| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:55580104-55580291 | Common:2; Rare:83 | ||||
| chr14:57268551-57268613 | Rare:16 | ||||
| chr14:57268812-57269094 | Common:2; Rare:87 | ||||
| chr14:58199866-58200207 | Common:3; Rare:128 | ||||
| chr14:58244646-58244918 | Rare:89 | ||||
| chr14:58298102-58298559 | Rare:109 | ||||
| chr14:58427076-58427432 | Common:2; Rare:85 | ||||
| chr14:58427529-58427749 | Rare:75 | ||||
| chr14:59484333-59484565 | Common:3; Rare:90 | ||||
| chr14:60980982-60981257 | Rare:110 | ||||
| chr14:61762211-61762437 | Common:4; Rare:64 | ||||
| chr14:63543336-63543587 | Common:3; Rare:62 | ||||
| chr14:63641813-63642081 | Common:4; Rare:86 | ||||
| chr14:63852873-63853041 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:64388234-64388385 | Common:2; Rare:81 |