| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:101071768-101071912 | Common:1; Rare:34 | ||||
| chr14:101071946-101072156 | Common:2; Rare:35 | ||||
| chr14:101948020-101948345 | Common:2; Rare:97 | ||||
| chr14:102029509-102029937 | Common:1; Rare:84; Clinvar:4; Clinvar (benign):4 | ||||
| chr14:102044398-102044698 | Common:2; Rare:73; Clinvar:4; Clinvar (benign):3 | ||||
| chr14:102082505-102082595 | Rare:36 | ||||
| chr14:102202977-102203127 | Common:1; Rare:30 | ||||
| chr14:102320949-102321220 | Rare:45 | ||||
| chr14:102330343-102330496 | Common:2; Rare:29 | ||||
| chr14:102333979-102334284 | Rare:48 | ||||
| chr14:102593204-102593306 | Rare:50 | ||||
| chr14:103462769-103463163 | Common:4; Rare:73 | ||||
| chr14:103463394-103463444 | Rare:8 | ||||
| chr14:103482749-103482843 | Common:1; Rare:12 | ||||
| chr14:103500909-103501011 | Common:2; Rare:24 |