DMR Stats
Positionchr1:6681901-6682050 (View on UCSC)
Width150bp
Genomic Contextexon
Nearest GenesPHF13 (0bp away)
ANODEV p-value0.000755101800442
FrequenciesBenign: 2.0 (28.57%), Low: 6.0 (100.0%), High: 9.0 (100.0 %)
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
24953 PHF13 159 uc001aob.4 chr1 6673756 6684093 + 150 100.0 0.46 0 0.0 E1 (0), I1 (0), E2 (0), I2 (0), E3 (0), I3 (0), E4 (100) 0.0
  • 1 genes

Feature Overlaps

Dmrid Feature Chr Feature Start Feature End Set Name Fields
24953 chr1 6681870 6682273 wgEncodeRegTfbsClusteredV3 POLR2A score:203, expCount:1, expNums:228, expScores:203, srow:15183
24953 chr1 6681889 6681903 phastConsElements100way lod=54 score:388, srow:24315
24953 chr1 6681906 6681908 phastConsElements100way lod=17 score:274, srow:24316
24953 chr1 6681974 6681978 phastConsElements100way lod=32 score:337, srow:24317
24953 chr1 6682030 6682031 phastConsElements100way lod=12 score:240, srow:24318
24953 chr1 6682037 6682040 phastConsElements100way lod=18 score:280, srow:24319
24953 chr1 6681072 6683071 cpgShelf values(x.gr)[overs$srow, ]:390
  • 7 featuress

Omics Overlaps

Dmrid Omic Set Data Plot
24953 cellmeth_recounts PrEC: 17, LNCaP: 18, DU145: 8
24953 cellmeth_diffreps_PrECvsDU145 A=177, B=13, Length=500, Event=Down, log2FC=-3.77, padj=0
24953 cellexp id=ENSG00000116273, name=PHF13, PrEC=2264, str=2611, LNCaP=1673, str=1572, DU145=1988, str=2081
24953 tcgaexp gene=SRSF10, entrez=10772, pos=chr1:36273-24306953(-), B=3487, L=3388, M=3432, H=4019
24953 tcgaexp gene=PHF13, entrez=148479, pos=chr1:6673756-6684093(+), B=1693, L=1505, M=1459, H=1621
24953 tcgaexp gene=LOC100133331, entrez=100133331, pos=chr1:322037-180753553(-), B=268, L=328, M=271, H=305