| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74493240-74493801 | Common:4; Rare:184; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713058-74713207 | Rare:81 | ||||
| chr14:75002666-75002947 | Common:1; Rare:85; Clinvar:2 | ||||
| chr14:75069489-75069673 | Common:1; Rare:43 | ||||
| chr14:75127036-75127110 | Rare:20 | ||||
| chr14:75660797-75661346 | Common:4; Rare:132 | ||||
| chr14:75981129-75981195 | Rare:9 | ||||
| chr14:76762544-76762846 | Rare:81 | ||||
| chr14:77377045-77377410 | Common:2; Rare:107 | ||||
| chr14:77457550-77457876 | Common:1; Rare:97 | ||||
| chr14:77707992-77708206 | Common:2; Rare:108 | ||||
| chr14:77761114-77761406 | Common:2; Rare:88 | ||||
| chr14:81220867-81221256 | Common:1; Rare:154 | ||||
| chr14:85530030-85530235 | Common:1; Rare:43 | ||||
| chr14:88824343-88824710 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):1 |