| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75660833-75661582 | Common:7; Rare:191 | ||||
| chr14:77097914-77098348 | Rare:140 | ||||
| chr14:77320767-77321105 | Common:2; Rare:99; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:77377060-77377473 | Common:3; Rare:128 | ||||
| chr14:77457529-77457891 | Common:2; Rare:108 | ||||
| chr14:77457987-77458262 | Rare:66 | ||||
| chr14:77707828-77708230 | Common:2; Rare:180 | ||||
| chr14:77710663-77710881 | Common:1; Rare:48 | ||||
| chr14:80211148-80211224 | Rare:24 | ||||
| chr14:80212016-80212391 | Common:4; Rare:68 | ||||
| chr14:80941678-80941945 | Common:3; Rare:61 | ||||
| chr14:81220693-81221059 | Common:3; Rare:140 | ||||
| chr14:81533725-81533909 | Common:1; Rare:64 | ||||
| chr14:85530007-85530190 | Common:1; Rare:38 | ||||
| chr14:87993117-87993260 | Common:2; Rare:69; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):2 |