| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:89955780-89956111 | Common:13; Rare:118; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89956155-89956298 | Rare:63 | ||||
| chr14:89956406-89956523 | Rare:31 | ||||
| chr14:89956553-89956600 | Common:3; Rare:9; Clinvar (benign):3 | ||||
| chr14:90256457-90256635 | Common:2; Rare:60 | ||||
| chr14:90331612-90331735 | Rare:35 | ||||
| chr14:90331910-90332411 | Common:1; Rare:127 | ||||
| chr14:90396733-90397112 | Common:4; Rare:181 | ||||
| chr14:90397493-90397759 | Common:3; Rare:92 | ||||
| chr14:90397996-90398197 | Common:4; Rare:44 | ||||
| chr14:90816358-90816537 | Common:1; Rare:38 | ||||
| chr14:91060002-91060070 | Common:1; Rare:19 | ||||
| chr14:91060122-91060399 | Common:3; Rare:100 | ||||
| chr14:91060548-91061204 | Common:3; Rare:179 | ||||
| chr14:91113992-91114140 | Rare:44 |