| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:94591220-94591564 | Common:2; Rare:49 | ||||
| chr14:94612180-94612472 | Common:2; Rare:72 | ||||
| chr14:95157327-95157740 | Common:4; Rare:143; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:95307503-95307710 | Rare:44 | ||||
| chr14:95533485-95533534 | Rare:20 | ||||
| chr14:95534560-95534674 | Rare:48 | ||||
| chr14:95534708-95534759 | Rare:16 | ||||
| chr14:95534775-95534809 | Rare:3 | ||||
| chr14:95535320-95535362 | Common:1; Rare:19; Clinvar (benign):1 | ||||
| chr14:95535368-95535371 | Rare:1 | ||||
| chr14:95714116-95714314 | Common:2; Rare:57 | ||||
| chr14:96363283-96363556 | Common:1; Rare:92 | ||||
| chr14:96391792-96392164 | Common:2; Rare:107 | ||||
| chr14:96502286-96502595 | Common:1; Rare:131 | ||||
| chr14:99480728-99480981 | Common:2; Rare:99 |