Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:90839092-90839204 | Common:1; Rare:19 | ||||
chr4:94468149-94468400 | Common:3; Rare:40 | ||||
chr4:99315898-99316292 | Rare:128 | ||||
chr4:118279110-118279190 | Common:3; Rare:20 | ||||
chr4:118591553-118591805 | Common:4; Rare:78 | ||||
chr4:119454582-119454861 | Common:13; Rare:96 | ||||
chr4:140094943-140095139 | Common:1; Rare:33 | ||||
chr4:147637145-147637187 | Rare:10 | ||||
chr4:151100825-151101158 | Rare:71 | ||||
chr4:153684143-153684299 | Common:1; Rare:52 | ||||
chr4:168903550-168903899 | Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
chr4:168923993-168924418 | Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
chr4:182814534-182814674 | Common:1; Rare:41 | ||||
chr5:282743-283057 | Common:1; Rare:41 | ||||
chr5:1633909-1634056 | Common:2; Rare:49 |