| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24429861-24429970 | Rare:23 | ||||
| chr14:24442681-24443013 | Common:5; Rare:107 | ||||
| chr14:31207662-31208030 | Common:2; Rare:128 | ||||
| chr14:31420496-31420709 | Common:4; Rare:77 | ||||
| chr14:32076017-32076312 | Common:2; Rare:75 | ||||
| chr14:32076672-32077041 | Common:3; Rare:111 | ||||
| chr14:34462205-34462558 | Common:1; Rare:123 | ||||
| chr14:34875299-34875454 | Rare:60 | ||||
| chr14:35046119-35046554 | Common:2; Rare:147 | ||||
| chr14:35121955-35122695 | Common:4; Rare:206 | ||||
| chr14:36320552-36320817 | Common:4; Rare:87 | ||||
| chr14:39267010-39267408 | Common:2; Rare:130 | ||||
| chr14:44961903-44962239 | Common:3; Rare:97 | ||||
| chr14:45253084-45253346 | Rare:76 | ||||
| chr14:49586297-49586766 | Common:1; Rare:241; Clinvar (benign):1 |