| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23409560-23409828 | Common:2; Rare:50 | ||||
| chr14:23414402-23414598 | Common:2; Rare:41 | ||||
| chr14:23415379-23415835 | Common:1; Rare:140; Clinvar:23; Clinvar (benign):14; Clinvar (pathogenic):5 | ||||
| chr14:23424767-23425420 | Common:1; Rare:164; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):13 | ||||
| chr14:23425693-23426085 | Common:1; Rare:96; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):9 | ||||
| chr14:23428953-23429349 | Rare:96; Clinvar:7; Clinvar (benign):13; Clinvar (pathogenic):6 | ||||
| chr14:23431416-23431679 | Common:1; Rare:67; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr14:23432477-23432825 | Rare:83; Clinvar:8; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
| chr14:23434192-23434295 | Common:1; Rare:21; Clinvar (benign):5 | ||||
| chr14:32203267-32203667 | Common:13; Rare:169 | ||||
| chr14:34874137-34874206 | Common:1; Rare:18 | ||||
| chr14:49633949-49634076 | Common:1; Rare:53; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:49862651-49862985 | Common:1; Rare:161 | ||||
| chr14:60642266-60642399 | Common:1; Rare:37 | ||||
| chr14:61751067-61751223 | Rare:41 |