| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74713049-74713207 | Rare:89 | ||||
| chr14:74763198-74763425 | Rare:76 | ||||
| chr14:74881801-74881975 | Common:1; Rare:79 | ||||
| chr14:75002720-75002982 | Common:1; Rare:86; Clinvar:2 | ||||
| chr14:75051418-75051523 | Common:2; Rare:30; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:75063983-75064184 | Common:1; Rare:50 | ||||
| chr14:75069471-75069677 | Common:2; Rare:51 | ||||
| chr14:75126994-75127128 | Rare:46 | ||||
| chr14:75660774-75661330 | Common:4; Rare:141 | ||||
| chr14:76151777-76151982 | Rare:71 | ||||
| chr14:76812819-76812998 | Common:1; Rare:76 | ||||
| chr14:77097980-77098369 | Rare:126 | ||||
| chr14:77320824-77321111 | Rare:91; Clinvar:2 | ||||
| chr14:77377030-77377198 | Common:2; Rare:56 | ||||
| chr14:77377339-77377443 | Rare:41 |