| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:57268814-57269125 | Common:2; Rare:92 | ||||
| chr14:57390462-57390665 | Rare:62 | ||||
| chr14:58199832-58200207 | Common:4; Rare:148 | ||||
| chr14:58244535-58244939 | Rare:126 | ||||
| chr14:58298084-58298439 | Rare:92 | ||||
| chr14:58427149-58427399 | Rare:55 | ||||
| chr14:59188409-59188757 | Common:2; Rare:93 | ||||
| chr14:59484321-59484565 | Common:3; Rare:98 | ||||
| chr14:60091834-60092270 | Common:4; Rare:160 | ||||
| chr14:60981017-60981257 | Rare:96 | ||||
| chr14:61695214-61695569 | Common:3; Rare:110 | ||||
| chr14:61762184-61762454 | Common:4; Rare:92 | ||||
| chr14:63543307-63543619 | Common:4; Rare:87 | ||||
| chr14:63641823-63642153 | Common:4; Rare:106 | ||||
| chr14:63852816-63853066 | Common:1; Rare:91; Clinvar:2; Clinvar (benign):2 |