| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49596377-49596845 | Common:4; Rare:117 | ||||
| chr14:49597326-49597820 | Common:3; Rare:158 | ||||
| chr14:49617280-49617690 | Common:4; Rare:130 | ||||
| chr14:49617689-49618496 | Common:14; Rare:269 | ||||
| chr14:49622039-49622666 | Rare:248; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):10 | ||||
| chr14:49624253-49624482 | Rare:74 | ||||
| chr14:49633824-49634188 | Common:4; Rare:363; Clinvar:40; Clinvar (benign):15; Clinvar (pathogenic):7 | ||||
| chr14:49634215-49634667 | Common:4; Rare:487; Clinvar:34; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr14:49840845-49841119 | Common:1; Rare:48 | ||||
| chr14:49853737-49854137 | Rare:75 | ||||
| chr14:49858364-49858764 | Common:2; Rare:100 | ||||
| chr14:49861430-49861600 | Rare:29 | ||||
| chr14:49861620-49862041 | Common:2; Rare:132 | ||||
| chr14:49862043-49862443 | Common:1; Rare:107 | ||||
| chr14:49862642-49863273 | Common:4; Rare:487 |