Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:74783029-74783203 | Common:1; Rare:30 | ||||
chr15:74787279-74788208 | Common:5; Rare:176 | ||||
chr15:74788449-74788619 | Common:1; Rare:36 | ||||
chr15:74788674-74789018 | Common:1; Rare:70 | ||||
chr15:74821397-74821580 | Rare:32 | ||||
chr15:74842672-74842942 | Rare:55 | ||||
chr15:74843077-74843360 | Common:2; Rare:83 | ||||
chr15:74872935-74873183 | Common:2; Rare:69 | ||||
chr15:74873225-74873529 | Common:6; Rare:80 | ||||
chr15:74889477-74889596 | Rare:27 | ||||
chr15:74889878-74890161 | Rare:101; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr15:74905972-74906296 | Rare:70 | ||||
chr15:74906704-74907017 | Common:1; Rare:118 | ||||
chr15:74937458-74937517 | Common:1; Rare:11 | ||||
chr15:74937581-74937800 | Rare:59 |