| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73786597-73787040 | Common:3; Rare:124 | ||||
| chr14:73787091-73787482 | Common:9; Rare:280 | ||||
| chr14:73851591-73852096 | Common:18; Rare:349 | ||||
| chr14:73886598-73887078 | Common:7; Rare:183 | ||||
| chr14:73887901-73888383 | Common:1; Rare:86 | ||||
| chr14:73949993-73950416 | Common:19; Rare:452; Clinvar (benign):15 | ||||
| chr14:73950510-73950796 | Common:1; Rare:97 | ||||
| chr14:74018997-74019463 | Common:9; Rare:352 | ||||
| chr14:74084144-74085008 | Common:17; Rare:390 | ||||
| chr14:74302870-74303157 | Common:6; Rare:275; Clinvar (benign):5 | ||||
| chr14:74493129-74493878 | Common:12; Rare:658; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr14:74493972-74494432 | Common:1; Rare:327; Clinvar (benign):6 | ||||
| chr14:74713008-74713248 | Common:2; Rare:347 | ||||
| chr14:74763069-74763481 | Rare:214 | ||||
| chr14:74763607-74764260 | Common:3; Rare:411 |