| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23953638-23953791 | Common:6; Rare:57 | ||||
| chr14:24115018-24115280 | Common:2; Rare:72 | ||||
| chr14:24146564-24146755 | Rare:63 | ||||
| chr14:24195410-24195715 | Common:1; Rare:69 | ||||
| chr14:24232305-24232687 | Common:8; Rare:93 | ||||
| chr14:24242272-24242433 | Rare:52; Clinvar (benign):2 | ||||
| chr14:24242586-24242732 | Common:1; Rare:30; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24299749-24299850 | Common:1; Rare:29 | ||||
| chr14:30559071-30559211 | Common:1; Rare:51 | ||||
| chr14:30622190-30622359 | Common:1; Rare:64 | ||||
| chr14:31420514-31420672 | Common:3; Rare:60 | ||||
| chr14:34539649-34539856 | Rare:56 | ||||
| chr14:34982504-34982696 | Common:1; Rare:81 | ||||
| chr14:35046089-35046387 | Common:1; Rare:105 | ||||
| chr14:35121955-35122614 | Common:3; Rare:187 |