| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35121913-35122751 | Common:4; Rare:243 | ||||
| chr14:35292177-35292463 | Common:4; Rare:105 | ||||
| chr14:35404635-35404814 | Common:2; Rare:74; Clinvar (benign):2 | ||||
| chr14:35809206-35809366 | Common:1; Rare:40 | ||||
| chr14:35826313-35826465 | Rare:36 | ||||
| chr14:36320580-36320783 | Common:3; Rare:63 | ||||
| chr14:37197813-37198103 | Common:3; Rare:97 | ||||
| chr14:38256077-38256319 | Common:1; Rare:59 | ||||
| chr14:39114137-39114335 | Common:2; Rare:61 | ||||
| chr14:39170203-39170471 | Common:3; Rare:72 | ||||
| chr14:39174916-39175292 | Common:5; Rare:134 | ||||
| chr14:39266828-39267422 | Common:3; Rare:206 | ||||
| chr14:39432438-39432657 | Common:6; Rare:75 | ||||
| chr14:44897065-44897352 | Common:1; Rare:101 | ||||
| chr14:44961892-44962259 | Common:3; Rare:106 |