| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91060168-91060393 | Common:3; Rare:90 | ||||
| chr14:91060546-91060812 | Common:2; Rare:84 | ||||
| chr14:91114049-91114406 | Common:1; Rare:88 | ||||
| chr14:91510215-91510644 | Common:1; Rare:146 | ||||
| chr14:91836452-91836701 | Common:12; Rare:48 | ||||
| chr14:91947618-91947819 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):4 | ||||
| chr14:92039756-92040181 | Common:3; Rare:107; Clinvar:7; Clinvar (benign):2 | ||||
| chr14:92106536-92106693 | Common:1; Rare:50 | ||||
| chr14:92121647-92122266 | Common:5; Rare:194 | ||||
| chr14:92513297-92513425 | Common:2; Rare:29 | ||||
| chr14:92748504-92748803 | Rare:72 | ||||
| chr14:92794038-92794456 | Rare:130 | ||||
| chr14:92923015-92923153 | Common:3; Rare:33 | ||||
| chr14:93184834-93185022 | Rare:67 | ||||
| chr14:93206977-93207316 | Common:3; Rare:171 |