| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88824343-88824716 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90331906-90332219 | Common:1; Rare:93 | ||||
| chr14:90396870-90397131 | Common:2; Rare:134 | ||||
| chr14:91060572-91060821 | Common:2; Rare:79 | ||||
| chr14:91510457-91510713 | Common:1; Rare:88 | ||||
| chr14:91836421-91836706 | Common:12; Rare:52 | ||||
| chr14:91947231-91947776 | Common:6; Rare:140; Clinvar:3; Clinvar (benign):9 | ||||
| chr14:92040019-92040192 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:92121655-92122000 | Common:5; Rare:116 | ||||
| chr14:93184856-93185005 | Rare:46 | ||||
| chr14:93206983-93207290 | Common:2; Rare:148 | ||||
| chr14:93332469-93332694 | Common:1; Rare:64 | ||||
| chr14:93976559-93976724 | Rare:37 | ||||
| chr14:94081123-94081387 | Common:5; Rare:83 | ||||
| chr14:95157430-95157707 | Common:4; Rare:98 |