| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50231828-50232041 | Common:1; Rare:82 | ||||
| chr14:50312122-50312412 | Common:1; Rare:128; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:50312570-50312714 | Common:6; Rare:54 | ||||
| chr14:50396879-50397046 | Common:2; Rare:52 | ||||
| chr14:50397117-50397256 | Rare:65 | ||||
| chr14:50532533-50532825 | Common:4; Rare:93 | ||||
| chr14:50560440-50560619 | Rare:46 | ||||
| chr14:50561007-50561155 | Rare:27 | ||||
| chr14:50668172-50668453 | Common:2; Rare:91 | ||||
| chr14:50830500-50830809 | Common:2; Rare:79 | ||||
| chr14:50831129-50831256 | Common:1; Rare:45 | ||||
| chr14:50831289-50832213 | Common:4; Rare:291 | ||||
| chr14:50944310-50944740 | Common:6; Rare:142; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51095071-51095553 | Common:5; Rare:170 | ||||
| chr14:51095644-51096184 | Common:4; Rare:133 |