| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24114996-24115319 | Common:2; Rare:90 | ||||
| chr14:24135951-24136299 | Common:1; Rare:110 | ||||
| chr14:24141577-24141862 | Common:1; Rare:61 | ||||
| chr14:24146559-24146935 | Common:2; Rare:112 | ||||
| chr14:24171988-24172119 | Rare:35 | ||||
| chr14:24195405-24195739 | Common:1; Rare:73 | ||||
| chr14:24213072-24213184 | Rare:19 | ||||
| chr14:24213431-24213622 | Common:1; Rare:62 | ||||
| chr14:24232295-24232714 | Common:8; Rare:104 | ||||
| chr14:24232800-24232953 | Common:1; Rare:31 | ||||
| chr14:24242264-24242408 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24242562-24242774 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24263148-24263302 | Common:2; Rare:39 | ||||
| chr14:24271418-24271611 | Common:1; Rare:54 | ||||
| chr14:24299706-24299858 | Common:4; Rare:44 |