Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:67837427-67837745 | Rare:55 | ||||
chr10:67838015-67838270 | Common:3; Rare:52 | ||||
chr10:67884355-67884402 | Rare:11 | ||||
chr10:67884418-67885226 | Common:7; Rare:296 | ||||
chr10:67885258-67885346 | Rare:28 | ||||
chr10:68074227-68074351 | Rare:27 | ||||
chr10:68074556-68075512 | Common:8; Rare:275 | ||||
chr10:68231363-68231700 | Common:1; Rare:119; Clinvar (pathogenic):2 | ||||
chr10:68332466-68332560 | Rare:26 | ||||
chr10:68332679-68333042 | Common:2; Rare:104 | ||||
chr10:68406418-68406624 | Rare:52 | ||||
chr10:68406746-68407138 | Common:2; Rare:128 | ||||
chr10:68407144-68407590 | Common:7; Rare:126 | ||||
chr10:68471694-68472063 | Common:2; Rare:152; Clinvar:1; Clinvar (benign):3 | ||||
chr10:68527031-68527279 | Common:1; Rare:56 |