| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113394022-113394174 | Common:2; Rare:46 | ||||
| chr14:23487093-23487155 | Rare:11 | ||||
| chr14:23512943-23513378 | Common:2; Rare:94 | ||||
| chr14:28764362-28764565 | Common:1; Rare:46 | ||||
| chr14:28766017-28766209 | Rare:48 | ||||
| chr14:28766514-28766779 | Common:2; Rare:85 | ||||
| chr14:28766790-28767016 | Common:1; Rare:61 | ||||
| chr14:28767889-28767953 | Rare:8; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr14:28768225-28768696 | Rare:110; Clinvar:4; Clinvar (benign):17; Clinvar (pathogenic):2 | ||||
| chr14:28770759-28770839 | Common:1; Rare:15 | ||||
| chr14:28773151-28773239 | Rare:18 | ||||
| chr14:28774479-28774839 | Common:4; Rare:65 | ||||
| chr14:28775042-28775177 | Rare:24 | ||||
| chr14:28778180-28778286 | Common:2; Rare:31 | ||||
| chr14:28784150-28784458 | Rare:52 |