| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50532916-50533150 | Common:2; Rare:51 | ||||
| chr14:50561082-50561117 | Rare:5 | ||||
| chr14:50561124-50561156 | Rare:6 | ||||
| chr14:50668301-50668556 | Common:3; Rare:92 | ||||
| chr14:50944356-50944555 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51240096-51240413 | Common:1; Rare:129 | ||||
| chr14:51651620-51651996 | Common:4; Rare:106 | ||||
| chr14:51989376-51989666 | Common:2; Rare:92 | ||||
| chr14:51999525-51999779 | Rare:55 | ||||
| chr14:52069057-52069152 | Common:2; Rare:16 | ||||
| chr14:52314062-52314320 | Common:2; Rare:67 | ||||
| chr14:52706946-52707300 | Common:3; Rare:132 | ||||
| chr14:52791437-52791756 | Common:1; Rare:110 | ||||
| chr14:53152364-53152424 | Rare:24 | ||||
| chr14:55027048-55027320 | Common:2; Rare:74 |