| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100222467-100222572 | Rare:15 | ||||
| chr14:100240564-100240681 | Rare:36 | ||||
| chr14:100285365-100285606 | Rare:75 | ||||
| chr14:100285667-100285873 | Rare:49 | ||||
| chr14:100318307-100318432 | Common:1; Rare:33 | ||||
| chr14:101121265-101121465 | Common:3; Rare:37 | ||||
| chr14:101722237-101722383 | Common:2; Rare:17 | ||||
| chr14:101947932-101948441 | Common:6; Rare:146 | ||||
| chr14:101948498-101948641 | Common:2; Rare:22 | ||||
| chr14:101965277-101965404 | Common:2; Rare:28 | ||||
| chr14:101991450-101991609 | Common:4; Rare:30; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:101992772-101992940 | Common:1; Rare:34 | ||||
| chr14:102088451-102088805 | Common:3; Rare:111 | ||||
| chr14:102103110-102103289 | Common:2; Rare:17 | ||||
| chr14:102140651-102140742 | Rare:29 |