| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:96502286-96502586 | Common:1; Rare:128 | ||||
| chr14:100065295-100065441 | Rare:23 | ||||
| chr14:100375427-100375769 | Common:2; Rare:51 | ||||
| chr14:100376269-100376502 | Common:3; Rare:78 | ||||
| chr14:101809684-101810034 | Rare:83 | ||||
| chr14:102027777-102028012 | Rare:49; Clinvar:1; Clinvar (benign):4 | ||||
| chr14:102083474-102083996 | Common:6; Rare:221 | ||||
| chr14:102084398-102085098 | Common:1; Rare:305 | ||||
| chr14:102085270-102085690 | Common:8; Rare:177 | ||||
| chr14:102086981-102087493 | Common:6; Rare:212 | ||||
| chr14:102139678-102139923 | Rare:85 | ||||
| chr14:102235415-102235727 | Rare:68 | ||||
| chr14:102362862-102363092 | Rare:103 | ||||
| chr14:103333969-103334241 | Common:1; Rare:112 | ||||
| chr14:103521089-103521325 | Common:1; Rare:78 |