| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73851773-73852004 | Common:5; Rare:77 | ||||
| chr14:73950074-73950360 | Common:6; Rare:127; Clinvar (benign):4 | ||||
| chr14:74019233-74019436 | Common:1; Rare:81 | ||||
| chr14:74084399-74084603 | Common:2; Rare:60 | ||||
| chr14:74493225-74493813 | Common:4; Rare:197; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713058-74713203 | Rare:79 | ||||
| chr14:74881790-74881970 | Common:1; Rare:81 | ||||
| chr14:75002563-75002972 | Common:1; Rare:118; Clinvar:2 | ||||
| chr14:75126945-75127104 | Rare:52 | ||||
| chr14:75176368-75176810 | Common:1; Rare:122 | ||||
| chr14:75278376-75278680 | Common:1; Rare:73 | ||||
| chr14:75278799-75279311 | Common:3; Rare:139 | ||||
| chr14:75279318-75279816 | Common:1; Rare:89 | ||||
| chr14:75279868-75280738 | Common:6; Rare:229 | ||||
| chr14:75578339-75578701 | Common:2; Rare:69; Clinvar (benign):1 |