DMR Stats
Positionchr16:661201-661700 (View on UCSC)
Width500bp
Genomic Contextintron
Nearest GenesRAB40C (0bp away)
ANODEV p-value0.000584424899601
FrequenciesBenign: 1.0 (14.29%), Low: 1.0 (16.67%), High: 8.0 (88.89 %)
Frequent?

Region Count Boxplot

Region Overview

Gene Overlaps

Dmrid Gene Symbol Gene Id Isoform Id Isoform Chr Isoform Start Isoform End Isoform Strand Overlap Bp Query Overlap Per Isoform Overlap Per Noncoding Promoter Per Exonintron Per End Per
40909 RAB40C 10685 uc002chq.3 chr16 640077 679273 + 500 100.0 0.47 0 0.0 E1 (0), I1 (0), E2 (0), I2 (100), E3 (0), I3 (0), E4 (0), I4 (0), E5 (0), I5 (0), E6 (0), I6 (0), E7 (0) 0.0
40909 RAB40C 10685 uc002chr.3 chr16 640173 679273 + 500 100.0 0.35 0 0.0 E1 (0), I1 (100), E2 (0), I2 (0), E3 (0), I3 (0), E4 (0), I4 (0), E5 (0), I5 (0), E6 (0) 0.0
40909 RAB40C 10685 uc021szt.1 chr16 639357 679273 + 500 100.0 0.39 0 0.0 E1 (0), I1 (0), E2 (0), I2 (100), E3 (0), I3 (0), E4 (0), I4 (0), E5 (0), I5 (0), E6 (0), I6 (0), E7 (0) 0.0
40909 RAB40C 10685 uc021szu.1 chr16 639669 679273 + 500 100.0 0.29 0 0.0 E1 (0), I1 (0), E2 (0), I2 (100), E3 (0), I3 (0), E4 (0), I4 (0), E5 (0), I5 (0), E6 (0), I6 (0), E7 (0) 0.0
40909 RAB40C 10685 uc021szv.1 chr16 640077 679273 + 500 100.0 0.2 0 0.0 E1 (0), I1 (0), E2 (0), I2 (100), E3 (0), I3 (0), E4 (0), I4 (0), E5 (0), I5 (0), E6 (0), I6 (0), E7 (0) 0.0
  • 5 geness

Feature Overlaps

Dmrid Feature Chr Feature Start Feature End Set Name Fields
40909 chr16 660826 661415 wgEncodeRegDnaseClusteredV2 70 score:1000, srow:427652
40909 chr16 661034 661433 wgEncodeRegTfbsClusteredV3 MXI1 score:339, expCount:1, expNums:441, expScores:339, srow:1443574
40909 chr16 661044 661375 wgEncodeRegTfbsClusteredV3 STAT3 score:223, expCount:3, expNums:567,568,569, expScores:205,223,210, srow:1443575
40909 chr16 661046 661385 wgEncodeRegTfbsClusteredV3 HDAC2 score:152, expCount:1, expNums:181, expScores:152, srow:1443576
40909 chr16 661051 661474 wgEncodeRegTfbsClusteredV3 CTCF score:1000, expCount:91, expNums:0,2,5,9,12,14,16,18,20,24,35,37,39,42,44,49,137,174,213,262,290,463,493,595,597,598,601,603,604,605,606,607,609,612,615,618,621,627,628,629,630,631,635,636,638,639,640,641,642,643,644,645,646,648,650,651,652,653,654,655,656,657,658,659,660,661,662,663,664,665,666,667,669,670,671,672,673,674,675,676,677,678,679,680,681,683,685,686,687,688,689, expScores:1000,401,1000,592,864,640,704,592,388,220,168,346,1000,294,839,224,1000,921,183,247,690,496,266,728,469,1000,439,452,547,679,426,407,801,637,377,221,284,862,1000,1000,881,1000,1000,580,462,223,215,266,365,263,300,623,558,316,689,743,373,927,607,361,378,225,553,971,346,429,1000,561,1000,918,661,804,387,114,1000,649,638,359,627,1000,606,843,277,471,118,1000,1000,1000,667,1000,158, srow:1443577
40909 chr16 661066 661441 wgEncodeRegTfbsClusteredV3 YY1 score:566, expCount:3, expNums:119,162,203, expScores:295,566,294, srow:1443578
40909 chr16 661089 661364 wgEncodeRegTfbsClusteredV3 EGR1 score:218, expCount:1, expNums:138, expScores:218, srow:1443579
40909 chr16 661090 661385 wgEncodeRegTfbsClusteredV3 BHLHE40 score:177, expCount:1, expNums:423, expScores:177, srow:1443580
40909 chr16 661099 661442 wgEncodeRegTfbsClusteredV3 GABPA score:298, expCount:1, expNums:140, expScores:298, srow:1443581
40909 chr16 661119 661400 wgEncodeRegTfbsClusteredV3 SMC3 score:255, expCount:2, expNums:313,450, expScores:255,169, srow:1443582
40909 chr16 661125 661390 wgEncodeRegTfbsClusteredV3 RAD21 score:1000, expCount:9, expNums:108,149,193,231,264,310,355,448,466, expScores:299,1000,1000,268,584,161,799,757,334, srow:1443583
40909 chr16 661127 661416 wgEncodeRegTfbsClusteredV3 ZNF143 score:518, expCount:1, expNums:361, expScores:518, srow:1443584
40909 chr16 661182 661351 wgEncodeRegTfbsClusteredV3 CTCFL score:166, expCount:1, expNums:214, expScores:166, srow:1443585
40909 chr16 661263 661279 tfbsConsSites V$YY1_01 score:876, zScore:1.98, srow:1869255
40909 chr16 660988 661438 oreganno OREG0023540 id:OREG0023540, srow:8403
40909 chr16 661630 661643 phastConsElements100way lod=14 score:255, srow:3213430
40909 chr16 661662 661668 phastConsElements100way lod=17 score:274, srow:3213431
40909 chr16 661694 661712 phastConsElements100way lod=26 score:316, srow:3213432
40909 chr16 661335 661335 gwasCatalog rs7204439 pubMedID:22993228, author:Williams FM, pubDate:2012-09-19, journal:Ann Rheum Dis, title:Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects., trait:Disc degeneration (lumbar), initSample:4,683 European ancestry individuals, replSample:NR, region:16p13.3, genes:RAB40C, riskAllele:rs7204439-C, riskAlFreq:0.42, pValue:4E-6, pValueDesc:, orOrBeta:.11, ci95:[0.065-0.155] unit increase, platform:Affymetrix & Illumina [2,552,511] (imputed), cnv:N, srow:5857
40909 chr16 660037 662036 cpgShelf values(x.gr)[overs$srow, ]:13443
  • 20 featuress

Omics Overlaps

Dmrid Omic Set Data Plot
40909 cellmeth_recounts PrEC: 53, LNCaP: 18, DU145: 4
40909 cellmeth_diffreps_PrECvsLNCaP A=0, B=12, Length=220, Event=Up, log2FC=Inf, padj=0.00157949948552458
40909 cellmeth_diffreps_PrECvsLNCaP A=79, B=9, Length=420, Event=Down, log2FC=-3.13, padj=1.53853878359442e-13
40909 cellmeth_diffreps_PrECvsDU145 A=79, B=1, Length=460, Event=Down, log2FC=-6.3, padj=0
40909 cellexp id=ENSG00000197562, name=RAB40C, PrEC=1266, str=1075, LNCaP=3058, str=1915, DU145=1377, str=938
40909 tcgaexp gene=RAB40C, entrez=57799, pos=chr16:639357-679273(+), B=1884, L=2091, M=2225, H=2141
40909 pubmed gene=RAB40C, G=6, GP=0, GC=2, GM=0, GPM=0, GCM=0