| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49892875-49893125 | Rare:110 | ||||
| chr14:50116548-50116691 | Rare:66 | ||||
| chr14:50312170-50312380 | Rare:91 | ||||
| chr14:50396829-50397003 | Common:3; Rare:53 | ||||
| chr14:50532488-50532797 | Common:3; Rare:98 | ||||
| chr14:50668340-50668556 | Common:3; Rare:84 | ||||
| chr14:50944356-50944580 | Common:4; Rare:82; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51240093-51240304 | Common:1; Rare:87 | ||||
| chr14:51554475-51554705 | Rare:44 | ||||
| chr14:51651454-51651473 | Rare:9 | ||||
| chr14:51651670-51652031 | Common:4; Rare:105 | ||||
| chr14:51989380-51989690 | Common:2; Rare:104 | ||||
| chr14:52707041-52707289 | Common:1; Rare:104 | ||||
| chr14:52791418-52791790 | Common:2; Rare:121 | ||||
| chr14:52951003-52951442 | Common:4; Rare:157 |