| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:60091809-60092338 | Common:8; Rare:193 | ||||
| chr14:60248981-60249257 | Common:3; Rare:105 | ||||
| chr14:60980998-60981283 | Rare:110 | ||||
| chr14:61322816-61322931 | Rare:19 | ||||
| chr14:61695178-61695586 | Common:3; Rare:129 | ||||
| chr14:61736709-61736964 | Common:2; Rare:55 | ||||
| chr14:61740309-61740573 | Common:1; Rare:51 | ||||
| chr14:61762201-61762470 | Common:5; Rare:114 | ||||
| chr14:63204241-63204482 | Rare:50 | ||||
| chr14:63543305-63543629 | Common:4; Rare:90 | ||||
| chr14:63641789-63642100 | Common:4; Rare:98 | ||||
| chr14:63852869-63853080 | Common:1; Rare:82; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:64196708-64197062 | Common:1; Rare:78 | ||||
| chr14:64218442-64218709 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:64388229-64388430 | Common:2; Rare:103 |