| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:30622190-30622379 | Common:1; Rare:91 | ||||
| chr14:31025618-31025653 | Rare:12 | ||||
| chr14:31420524-31420763 | Common:3; Rare:71 | ||||
| chr14:31457401-31457584 | Common:2; Rare:58 | ||||
| chr14:31561089-31561442 | Common:4; Rare:95; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076667-32077018 | Common:3; Rare:106 | ||||
| chr14:34462213-34462593 | Common:1; Rare:130 | ||||
| chr14:34630072-34630260 | Common:5; Rare:89 | ||||
| chr14:34714536-34714738 | Common:2; Rare:76 | ||||
| chr14:34875271-34875381 | Rare:46 | ||||
| chr14:34982510-34982712 | Common:1; Rare:87 | ||||
| chr14:35046148-35046566 | Common:1; Rare:143 | ||||
| chr14:35121925-35122625 | Common:3; Rare:203 | ||||
| chr14:35292246-35292479 | Common:4; Rare:86; Clinvar:1 | ||||
| chr14:35404651-35404740 | Common:2; Rare:48; Clinvar (benign):2 |