| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49586327-49586800 | Common:1; Rare:249; Clinvar (benign):1 | ||||
| chr14:49598666-49598703 | Rare:13 | ||||
| chr14:49598731-49599036 | Common:1; Rare:110 | ||||
| chr14:49620574-49620903 | Common:2; Rare:125; Clinvar:4 | ||||
| chr14:49688199-49688278 | Rare:29 | ||||
| chr14:49767664-49767757 | Common:1; Rare:25 | ||||
| chr14:49768696-49768988 | Rare:75 | ||||
| chr14:49780658-49780762 | Rare:20 | ||||
| chr14:49795844-49796038 | Rare:41 | ||||
| chr14:49892889-49893221 | Rare:133 | ||||
| chr14:50312140-50312384 | Common:1; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:50396702-50396995 | Common:5; Rare:84 | ||||
| chr14:50532455-50532801 | Common:4; Rare:106 | ||||
| chr14:50533159-50533311 | Common:1; Rare:25 | ||||
| chr14:50668327-50668556 | Common:3; Rare:85 |