| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75279515-75279660 | Rare:28 | ||||
| chr14:75427610-75427749 | Rare:36 | ||||
| chr14:75660813-75661330 | Common:4; Rare:124 | ||||
| chr14:76310534-76310834 | Common:3; Rare:52 | ||||
| chr14:76762653-76762966 | Rare:104 | ||||
| chr14:77098011-77098385 | Rare:113 | ||||
| chr14:77377045-77377411 | Common:2; Rare:107 | ||||
| chr14:77457550-77457886 | Common:2; Rare:99 | ||||
| chr14:77708000-77708188 | Common:2; Rare:97 | ||||
| chr14:77761126-77761228 | Rare:44 | ||||
| chr14:81220855-81221059 | Common:1; Rare:98 | ||||
| chr14:81221329-81221635 | Common:1; Rare:97 | ||||
| chr14:85529885-85530190 | Common:2; Rare:65 | ||||
| chr14:87993045-87993306 | Common:4; Rare:122; Clinvar:12; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr14:88562751-88563136 | Rare:151 |