| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:90396870-90397140 | Common:2; Rare:136 | ||||
| chr14:91060551-91060783 | Common:1; Rare:75 | ||||
| chr14:91060947-91061162 | Rare:49 | ||||
| chr14:91114002-91114105 | Rare:30 | ||||
| chr14:91114569-91114677 | Common:1; Rare:11 | ||||
| chr14:91510251-91510717 | Common:1; Rare:162 | ||||
| chr14:91836448-91836681 | Common:12; Rare:42 | ||||
| chr14:91947504-91947776 | Common:2; Rare:81; Clinvar:3; Clinvar (benign):4 | ||||
| chr14:92040023-92040177 | Common:2; Rare:45; Clinvar (benign):1 | ||||
| chr14:92106548-92106780 | Common:2; Rare:76 | ||||
| chr14:92121649-92122021 | Common:5; Rare:129 | ||||
| chr14:92154121-92154405 | Rare:56 | ||||
| chr14:92748546-92748803 | Rare:67 | ||||
| chr14:92793977-92794408 | Rare:139 | ||||
| chr14:93115196-93115474 | Common:2; Rare:108 |