| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88824361-88824710 | Common:2; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:89619097-89619260 | Common:1; Rare:58 | ||||
| chr14:90332033-90332408 | Rare:81 | ||||
| chr14:90396998-90397233 | Common:5; Rare:114; Clinvar (benign):2 | ||||
| chr14:90398383-90398487 | Common:1; Rare:30 | ||||
| chr14:91060122-91060393 | Common:3; Rare:97 | ||||
| chr14:91060553-91060647 | Rare:35 | ||||
| chr14:91060650-91060829 | Common:2; Rare:56 | ||||
| chr14:91114272-91114402 | Rare:23 | ||||
| chr14:91244664-91244832 | Common:2; Rare:30 | ||||
| chr14:91510242-91510627 | Common:1; Rare:122 | ||||
| chr14:91836410-91836681 | Common:12; Rare:46 | ||||
| chr14:91947977-91948196 | Common:4; Rare:33 | ||||
| chr14:92040019-92040192 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:92121655-92121990 | Common:5; Rare:110 |