| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49767514-49767614 | Rare:45 | ||||
| chr14:49767565-49767711 | Common:2; Rare:54 | ||||
| chr14:49768000-49768263 | Common:4; Rare:186 | ||||
| chr14:49768490-49769150 | Rare:322 | ||||
| chr14:49852741-49853141 | Common:3; Rare:106 | ||||
| chr14:49892879-49893157 | Rare:234 | ||||
| chr14:50116557-50116731 | Common:2; Rare:154 | ||||
| chr14:50231518-50232170 | Common:3; Rare:280 | ||||
| chr14:50312067-50312387 | Common:2; Rare:225; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:50396774-50397023 | Common:6; Rare:110 | ||||
| chr14:50531960-50533062 | Common:17; Rare:408 | ||||
| chr14:50668179-50668565 | Common:10; Rare:236 | ||||
| chr14:50831117-50831296 | Common:1; Rare:63 | ||||
| chr14:50944358-50944668 | Common:7; Rare:154; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:51239952-51240378 | Common:4; Rare:258 |