| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22589109-22589575 | Common:4; Rare:140 | ||||
| chr14:22598183-22598545 | Common:2; Rare:119 | ||||
| chr14:22766479-22766971 | Common:4; Rare:229 | ||||
| chr14:22767128-22767274 | Rare:41 | ||||
| chr14:22814895-22815136 | Common:2; Rare:37 | ||||
| chr14:22815326-22815378 | Common:1; Rare:17; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:22815379-22815784 | Common:1; Rare:86 | ||||
| chr14:22815804-22816048 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr14:22819194-22819370 | Common:1; Rare:34 | ||||
| chr14:22819566-22819903 | Common:4; Rare:69; Clinvar:3; Clinvar (benign):3 | ||||
| chr14:22819906-22819947 | Rare:7 | ||||
| chr14:22821271-22821628 | Common:3; Rare:60 | ||||
| chr14:22822535-22822669 | Rare:31 | ||||
| chr14:22822694-22823059 | Common:4; Rare:82 | ||||
| chr14:22823257-22823586 | Common:3; Rare:56 |