| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74465029-74465199 | Common:2; Rare:68; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:74465327-74465439 | Rare:29; Clinvar:1 | ||||
| chr2:74482955-74483097 | Common:1; Rare:51 | ||||
| chr2:74483268-74483387 | Common:1; Rare:50 | ||||
| chr2:74503357-74503475 | Rare:27 | ||||
| chr2:74529653-74530053 | Rare:126; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530348-74530626 | Common:4; Rare:90; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:74553100-74553136 | Common:1; Rare:9 | ||||
| chr2:74553777-74554042 | Rare:41 | ||||
| chr2:74554406-74554761 | Common:2; Rare:107 | ||||
| chr2:74833915-74834173 | Rare:74 | ||||
| chr2:74835141-74835316 | Rare:46 | ||||
| chr2:74958596-74959086 | Common:4; Rare:200 | ||||
| chr2:75560854-75561254 | Common:3; Rare:99 | ||||
| chr2:75561257-75561608 | Common:3; Rare:48 |