| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:99269624-99269723 | Common:1; Rare:19 | ||||
| chr14:99272093-99272216 | Rare:21 | ||||
| chr14:99298987-99299220 | Common:3; Rare:41 | ||||
| chr14:99942961-99943010 | Rare:7 | ||||
| chr14:100274712-100274797 | Rare:11 | ||||
| chr14:100366494-100366606 | Rare:20 | ||||
| chr14:100829109-100829189 | Rare:12 | ||||
| chr14:101843773-101843849 | Rare:16 | ||||
| chr14:101979420-101979755 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:101994981-101995294 | Rare:61; Clinvar:2; Clinvar (benign):5 | ||||
| chr14:102001227-102001682 | Common:3; Rare:95; Clinvar:6; Clinvar (benign):8 | ||||
| chr14:102009794-102009905 | Rare:28; Clinvar (benign):2 | ||||
| chr14:102017133-102017498 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:102081817-102082227 | Common:5; Rare:146 | ||||
| chr14:102083253-102083666 | Common:5; Rare:160 |