Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:12043135-12043438 | Common:2; Rare:89 | ||||
chr10:12129433-12129719 | Rare:121 | ||||
chr10:12195784-12195990 | Rare:52 | ||||
chr10:13099949-13100273 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13300037-13300164 | Rare:49; Clinvar:1 | ||||
chr10:13348006-13348370 | Rare:123 | ||||
chr10:13707163-13707295 | Common:2; Rare:24 | ||||
chr10:13707550-13707626 | Rare:16 | ||||
chr10:13971806-13972109 | Common:2; Rare:64 | ||||
chr10:14008148-14008366 | Rare:53 | ||||
chr10:14571989-14572223 | Common:3; Rare:45 | ||||
chr10:14837978-14838405 | Common:4; Rare:126 | ||||
chr10:14878588-14878891 | Common:2; Rare:95 | ||||
chr10:14953977-14954202 | Rare:80; Clinvar (benign):1 | ||||
chr10:14954322-14954348 | Rare:2 |