Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160262390-160262634 | Common:1; Rare:72 | ||||
chr1:160343181-160343409 | Rare:92 | ||||
chr1:160400374-160400584 | Common:1; Rare:55 | ||||
chr1:160739157-160739293 | Rare:38 | ||||
chr1:161021122-161021237 | Rare:31 | ||||
chr1:161045878-161046064 | Common:1; Rare:48 | ||||
chr1:161117955-161118134 | Rare:84 | ||||
chr1:161132411-161132700 | Common:1; Rare:94 | ||||
chr1:161153709-161153792 | Rare:20 | ||||
chr1:161159392-161159517 | Common:1; Rare:34 | ||||
chr1:161166268-161166499 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161225733-161226069 | Common:10; Rare:50 | ||||
chr1:161314260-161314443 | Common:4; Rare:76; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:161512911-161513461 | Common:2; Rare:91 | ||||
chr1:161513529-161513910 | Common:2; Rare:67 |