| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75069387-75069648 | Common:1; Rare:70 | ||||
| chr14:75126776-75127132 | Common:2; Rare:118 | ||||
| chr14:75176376-75176411 | Rare:7 | ||||
| chr14:75176571-75176653 | Rare:38 | ||||
| chr14:75280357-75280663 | Common:2; Rare:69 | ||||
| chr14:75427873-75428022 | Rare:27 | ||||
| chr14:75631266-75631386 | Common:2; Rare:24 | ||||
| chr14:75660770-75661501 | Common:7; Rare:194 | ||||
| chr14:75661507-75661668 | Common:1; Rare:26 | ||||
| chr14:76151778-76151991 | Rare:74 | ||||
| chr14:77028670-77028961 | Rare:94 | ||||
| chr14:77097980-77098373 | Rare:126 | ||||
| chr14:77141703-77141934 | Common:1; Rare:32 | ||||
| chr14:77142779-77142849 | Common:1; Rare:15 | ||||
| chr14:77320776-77321179 | Common:2; Rare:125; Clinvar:3; Clinvar (benign):2 |