| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50532469-50532798 | Common:3; Rare:103 | ||||
| chr14:50667828-50667969 | Rare:60 | ||||
| chr14:50668174-50668472 | Common:3; Rare:97 | ||||
| chr14:50668505-50668573 | Common:2; Rare:33 | ||||
| chr14:50668597-50668655 | Common:4; Rare:36 | ||||
| chr14:50821722-50821865 | Rare:36 | ||||
| chr14:50830564-50830828 | Common:2; Rare:68 | ||||
| chr14:50831097-50831393 | Common:1; Rare:97 | ||||
| chr14:50831552-50831719 | Rare:34 | ||||
| chr14:50944474-50944573 | Common:4; Rare:26; Clinvar (benign):1 | ||||
| chr14:51239953-51240354 | Common:2; Rare:132 | ||||
| chr14:51240474-51240537 | Common:2; Rare:32 | ||||
| chr14:51651361-51651479 | Common:1; Rare:37 | ||||
| chr14:51651508-51651954 | Common:4; Rare:114 | ||||
| chr14:51846611-51846768 | Rare:30 |