Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102056100-102056366 | Common:1; Rare:64 | ||||
chr10:102120477-102120565 | Common:1; Rare:31 | ||||
chr10:102394321-102394582 | Common:1; Rare:69 | ||||
chr10:102395553-102395933 | Common:1; Rare:86 | ||||
chr10:102714264-102714643 | Common:2; Rare:127 | ||||
chr10:102776078-102776279 | Common:1; Rare:34 | ||||
chr10:103193248-103193369 | Common:5; Rare:41; Clinvar (benign):1 | ||||
chr10:103396411-103396699 | Rare:103 | ||||
chr10:103452199-103452375 | Rare:47 | ||||
chr10:103452383-103452458 | Rare:20 | ||||
chr10:103917789-103917888 | Rare:18 | ||||
chr10:104121698-104122171 | Common:4; Rare:155 | ||||
chr10:104268956-104269185 | Common:3; Rare:52 | ||||
chr10:104338397-104338541 | Rare:39 | ||||
chr10:110005930-110006095 | Common:3; Rare:51 |