Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102056102-102056368 | Common:1; Rare:63 | ||||
chr10:102395536-102395684 | Common:1; Rare:36 | ||||
chr10:102420997-102421228 | Rare:97 | ||||
chr10:102432530-102432781 | Common:1; Rare:74 | ||||
chr10:102645083-102645131 | Rare:11 | ||||
chr10:102714271-102714609 | Common:2; Rare:116 | ||||
chr10:102776074-102776266 | Common:1; Rare:30 | ||||
chr10:102854214-102854299 | Rare:35 | ||||
chr10:103193248-103193321 | Common:4; Rare:23; Clinvar (benign):1 | ||||
chr10:103396411-103396699 | Rare:103 | ||||
chr10:103452242-103452453 | Rare:64 | ||||
chr10:103917789-103917871 | Rare:15 | ||||
chr10:103967018-103967048 | Rare:2 | ||||
chr10:104121753-104122171 | Common:3; Rare:139 | ||||
chr10:104338333-104338573 | Rare:62 |