Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:13707540-13707740 | Rare:46 | ||||
chr10:14008421-14008635 | Common:1; Rare:49 | ||||
chr10:14838002-14838393 | Common:2; Rare:112 | ||||
chr10:14878606-14878901 | Common:2; Rare:94 | ||||
chr10:14953977-14954195 | Rare:75; Clinvar (benign):1 | ||||
chr10:15043800-15043982 | Rare:43 | ||||
chr10:15097299-15097401 | Common:1; Rare:52 | ||||
chr10:15860455-15860572 | Rare:34 | ||||
chr10:16817337-16817734 | Common:4; Rare:141 | ||||
chr10:17228006-17228241 | Common:2; Rare:45 | ||||
chr10:17228355-17228675 | Common:4; Rare:83 | ||||
chr10:17228796-17229026 | Common:3; Rare:58 | ||||
chr10:17230526-17230717 | Rare:80; Clinvar:1 | ||||
chr10:17643866-17644315 | Common:2; Rare:140 | ||||
chr10:18651543-18651741 | Common:1; Rare:83 |