Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102420746-102420836 | Rare:21 | ||||
chr10:102421002-102421236 | Rare:100 | ||||
chr10:102713909-102713998 | Rare:12 | ||||
chr10:102714188-102714669 | Common:2; Rare:155 | ||||
chr10:102776078-102776234 | Common:1; Rare:25 | ||||
chr10:102854190-102854299 | Rare:44 | ||||
chr10:102869439-102869573 | Common:8; Rare:34 | ||||
chr10:103193248-103193480 | Common:5; Rare:72; Clinvar (benign):1 | ||||
chr10:103350886-103351161 | Common:1; Rare:113 | ||||
chr10:103396386-103396709 | Rare:118 | ||||
chr10:103918095-103918511 | Common:4; Rare:114 | ||||
chr10:103966985-103967249 | Common:1; Rare:84 | ||||
chr10:104121900-104122193 | Common:2; Rare:99 | ||||
chr10:104231761-104231870 | Common:1; Rare:19 | ||||
chr10:104254716-104254788 | Common:1; Rare:15 |