Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:22849621-22849721 | Common:2; Rare:17 | ||||
chr10:24238341-24238504 | Rare:17 | ||||
chr10:24266485-24266785 | Common:2; Rare:66 | ||||
chr10:24365569-24365610 | Rare:6 | ||||
chr10:24477005-24477340 | Common:3; Rare:55 | ||||
chr10:24724617-24724841 | Rare:71 | ||||
chr10:24850579-24850701 | Rare:27 | ||||
chr10:25934993-25935066 | Common:1; Rare:15 | ||||
chr10:26147291-26147467 | Common:2; Rare:34; Clinvar (pathogenic):1 | ||||
chr10:26152415-26152550 | Common:1; Rare:18 | ||||
chr10:26200707-26200858 | Rare:27 | ||||
chr10:26579362-26579561 | Common:1; Rare:22 | ||||
chr10:26637525-26637839 | Common:1; Rare:67 | ||||
chr10:26640151-26640292 | Rare:24 | ||||
chr10:26641572-26641598 | Rare:3 |