| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:76151726-76151995 | Rare:97 | ||||
| chr14:76152378-76152661 | Common:3; Rare:62 | ||||
| chr14:76812508-76812646 | Common:2; Rare:28 | ||||
| chr14:76812768-76813029 | Common:2; Rare:105 | ||||
| chr14:77028373-77028533 | Common:3; Rare:44 | ||||
| chr14:77028581-77029025 | Common:1; Rare:139 | ||||
| chr14:77097704-77098337 | Common:1; Rare:192 | ||||
| chr14:77320303-77320518 | Common:2; Rare:68; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr14:77320803-77321099 | Common:2; Rare:93; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:77321179-77321537 | Common:7; Rare:174 | ||||
| chr14:77321717-77321951 | Common:4; Rare:53 | ||||
| chr14:77376649-77376723 | Common:1; Rare:19 | ||||
| chr14:77376844-77377144 | Common:5; Rare:86 | ||||
| chr14:77377333-77377417 | Common:1; Rare:24 | ||||
| chr14:77457454-77457869 | Common:3; Rare:128 |