| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31208137-31208196 | Rare:13 | ||||
| chr14:31420514-31420755 | Common:3; Rare:76 | ||||
| chr14:31457385-31457580 | Common:2; Rare:67 | ||||
| chr14:31561088-31561463 | Common:4; Rare:102; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076128-32076326 | Rare:58 | ||||
| chr14:32076713-32077045 | Common:3; Rare:104 | ||||
| chr14:34462188-34462522 | Rare:122 | ||||
| chr14:34713090-34713365 | Common:2; Rare:63; Clinvar (benign):2 | ||||
| chr14:34714538-34714766 | Common:3; Rare:82 | ||||
| chr14:34875271-34875433 | Rare:64 | ||||
| chr14:34982484-34982682 | Common:1; Rare:83 | ||||
| chr14:35046089-35046580 | Common:2; Rare:167 | ||||
| chr14:35122206-35122781 | Common:2; Rare:165 | ||||
| chr14:35292179-35292620 | Common:5; Rare:140; Clinvar:1 | ||||
| chr14:35402746-35403174 | Common:5; Rare:131; Clinvar (benign):4 |