| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74555624-74555798 | Common:1; Rare:50 | ||||
| chr2:74654069-74654295 | Common:1; Rare:65 | ||||
| chr2:74958388-74958701 | Common:6; Rare:97 | ||||
| chr2:74958872-74959071 | Rare:72 | ||||
| chr2:75199513-75199788 | Common:2; Rare:53 | ||||
| chr2:75710627-75710784 | Common:2; Rare:62 | ||||
| chr2:84459219-84459581 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905484-84905962 | Common:2; Rare:145 | ||||
| chr2:85327915-85328080 | Common:2; Rare:74 | ||||
| chr2:85354491-85354792 | Common:1; Rare:100 | ||||
| chr2:85539072-85539195 | Common:2; Rare:54 | ||||
| chr2:85561425-85561603 | Rare:64; Clinvar:4 | ||||
| chr2:85584307-85584493 | Common:2; Rare:55 | ||||
| chr2:85595549-85595838 | Common:2; Rare:98 | ||||
| chr2:85602608-85602915 | Rare:80 |