| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74507256-74507452 | Rare:51 | ||||
| chr2:74507639-74507733 | Rare:27 | ||||
| chr2:74527458-74527742 | Common:1; Rare:95 | ||||
| chr2:74529585-74530030 | Rare:142; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:74530434-74530616 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74553941-74554171 | Rare:49 | ||||
| chr2:74554411-74554769 | Common:2; Rare:111 | ||||
| chr2:74555624-74555913 | Common:1; Rare:83 | ||||
| chr2:74654113-74654322 | Rare:59 | ||||
| chr2:74958332-74958772 | Common:7; Rare:149 | ||||
| chr2:74958867-74959011 | Rare:57 | ||||
| chr2:75199513-75199788 | Common:2; Rare:53 | ||||
| chr2:75654605-75654800 | Common:1; Rare:56 | ||||
| chr2:75710622-75710770 | Common:2; Rare:60 | ||||
| chr2:75710857-75711132 | Common:2; Rare:84 |