| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77923680-77924089 | Common:5; Rare:160 | ||||
| chr14:80941217-80941617 | Common:2; Rare:132 | ||||
| chr14:80941644-80942052 | Common:18; Rare:320 | ||||
| chr14:80954968-80955220 | Common:8; Rare:81 | ||||
| chr14:81220800-81221247 | Common:7; Rare:830 | ||||
| chr14:81221220-81221625 | Common:6; Rare:541 | ||||
| chr14:81221630-81222429 | Common:4; Rare:255 | ||||
| chr14:81427260-81427620 | Common:6; Rare:135 | ||||
| chr14:81427697-81428097 | Common:5; Rare:254 | ||||
| chr14:81435489-81436168 | Common:7; Rare:259 | ||||
| chr14:81436311-81436711 | Common:23; Rare:656 | ||||
| chr14:81533753-81534219 | Common:2; Rare:361 | ||||
| chr14:87992359-87993520 | Common:33; Rare:1285; Clinvar:84; Clinvar (benign):41; Clinvar (pathogenic):24 | ||||
| chr14:88385440-88385840 | Common:5; Rare:242; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:88551251-88551747 | Common:10; Rare:247 |