| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73950086-73950323 | Common:5; Rare:93; Clinvar (benign):3 | ||||
| chr14:74019263-74019432 | Common:1; Rare:66 | ||||
| chr14:74493240-74493777 | Common:4; Rare:171; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713052-74713223 | Rare:95 | ||||
| chr14:75002605-75003026 | Common:1; Rare:135; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75660813-75661326 | Common:4; Rare:122 | ||||
| chr14:77098053-77098348 | Rare:84 | ||||
| chr14:77320727-77321046 | Common:4; Rare:86; Clinvar:4; Clinvar (benign):3 | ||||
| chr14:77377028-77377411 | Common:3; Rare:111 | ||||
| chr14:77457536-77457886 | Common:2; Rare:105 | ||||
| chr14:77707987-77708133 | Common:1; Rare:76 | ||||
| chr14:81220871-81221046 | Common:1; Rare:85 | ||||
| chr14:81221275-81221471 | Common:1; Rare:49 | ||||
| chr14:85529991-85530235 | Common:1; Rare:50 | ||||
| chr14:89619125-89619272 | Rare:55 |