| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91060490-91060744 | Common:1; Rare:82 | ||||
| chr14:91060967-91061221 | Rare:63 | ||||
| chr14:91114002-91114030 | Rare:3 | ||||
| chr14:91114032-91114222 | Common:1; Rare:62 | ||||
| chr14:91114265-91114399 | Rare:24 | ||||
| chr14:91114559-91114704 | Common:2; Rare:14 | ||||
| chr14:91114757-91114800 | Common:1; Rare:5 | ||||
| chr14:91253400-91253540 | Common:1; Rare:44 | ||||
| chr14:91417143-91417505 | Common:3; Rare:89 | ||||
| chr14:91417514-91417711 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr14:91417728-91418042 | Common:5; Rare:93 | ||||
| chr14:91418089-91418361 | Common:1; Rare:75 | ||||
| chr14:91509128-91509165 | Common:2; Rare:11 | ||||
| chr14:91509492-91509779 | Common:1; Rare:109 | ||||
| chr14:91509791-91509919 | Rare:33 |