Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32650313-32650702 | Common:1; Rare:143 | ||||
chr1:32650898-32651354 | Common:2; Rare:168 | ||||
chr1:32651626-32651687 | Common:2; Rare:14 | ||||
chr1:32741470-32741601 | Rare:28 | ||||
chr1:32741733-32741866 | Common:1; Rare:45 | ||||
chr1:32742333-32742584 | Common:1; Rare:53 | ||||
chr1:32816637-32816740 | Common:1; Rare:21 | ||||
chr1:32816907-32816991 | Rare:15 | ||||
chr1:32817215-32817768 | Common:1; Rare:151; Clinvar:5; Clinvar (benign):3 | ||||
chr1:32817978-32818136 | Common:2; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
chr1:32818138-32818243 | Rare:28 | ||||
chr1:32901314-32901600 | Common:1; Rare:60 | ||||
chr1:32963816-32964253 | Rare:100 | ||||
chr1:32964750-32965037 | Common:2; Rare:112 | ||||
chr1:33036221-33036417 | Rare:31 |