| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:101991420-101991660 | Common:8; Rare:83; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr14:101992700-101993320 | Common:6; Rare:150 | ||||
| chr14:102087956-102088251 | Common:7; Rare:84 | ||||
| chr14:102088529-102088850 | Common:1; Rare:144 | ||||
| chr14:102140521-102140643 | Common:1; Rare:29 | ||||
| chr14:102314180-102314500 | Common:4; Rare:75 | ||||
| chr14:102344027-102345067 | Common:6; Rare:223 | ||||
| chr14:102370320-102370720 | Common:4; Rare:83 | ||||
| chr14:102516597-102517212 | Common:4; Rare:195 | ||||
| chr14:102524600-102525063 | Common:6; Rare:147 | ||||
| chr14:102554790-102555480 | Common:2; Rare:254 | ||||
| chr14:102555640-102555920 | Common:3; Rare:86 | ||||
| chr14:102591495-102591976 | Common:8; Rare:197 | ||||
| chr14:102607990-102608430 | Common:5; Rare:152 | ||||
| chr14:102645890-102646250 | Rare:63 |