| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100214034-100214215 | Common:1; Rare:52 | ||||
| chr14:100214406-100214689 | Common:2; Rare:90 | ||||
| chr14:100221604-100221775 | Rare:37 | ||||
| chr14:100240572-100240685 | Rare:37 | ||||
| chr14:100285334-100285589 | Rare:75 | ||||
| chr14:100285677-100285761 | Rare:17 | ||||
| chr14:100318092-100318492 | Common:1; Rare:84 | ||||
| chr14:101120754-101120874 | Common:2; Rare:18 | ||||
| chr14:101722087-101722355 | Common:2; Rare:38 | ||||
| chr14:101947959-101948431 | Common:6; Rare:138 | ||||
| chr14:101948509-101948631 | Common:2; Rare:19 | ||||
| chr14:101965273-101965372 | Common:2; Rare:24 | ||||
| chr14:101991450-101991635 | Common:4; Rare:35; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:101992789-101992929 | Common:1; Rare:29 | ||||
| chr14:102088491-102088788 | Common:2; Rare:94 |