| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75002741-75002982 | Common:2; Rare:151; Clinvar:4 | ||||
| chr14:75051378-75051530 | Common:4; Rare:75; Clinvar:6; Clinvar (benign):4 | ||||
| chr14:75063951-75064184 | Common:2; Rare:111 | ||||
| chr14:75069362-75069670 | Common:3; Rare:130 | ||||
| chr14:75126848-75127244 | Common:4; Rare:179 | ||||
| chr14:75175960-75176370 | Common:3; Rare:125 | ||||
| chr14:75176493-75177150 | Common:2; Rare:216 | ||||
| chr14:75278225-75278996 | Common:8; Rare:278 | ||||
| chr14:75279360-75279890 | Common:2; Rare:168 | ||||
| chr14:75427910-75428043 | Rare:18 | ||||
| chr14:75427954-75428085 | Rare:21 | ||||
| chr14:75578466-75578700 | Common:4; Rare:76; Clinvar (benign):2 | ||||
| chr14:75660789-75661479 | Common:12; Rare:331 | ||||
| chr14:75981830-75982370 | Common:4; Rare:125 | ||||
| chr14:76151754-76151955 | Rare:72 |