| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69387167-69387419 | Rare:74; Clinvar:2 | ||||
| chr2:70258037-70258156 | Common:1; Rare:38 | ||||
| chr2:70293661-70293891 | Common:3; Rare:74 | ||||
| chr2:71130225-71130322 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71130531-71130662 | Common:2; Rare:37 | ||||
| chr2:71276450-71276599 | Rare:44 | ||||
| chr2:73234220-73234361 | Common:1; Rare:44 | ||||
| chr2:73828804-73829005 | Common:1; Rare:45 | ||||
| chr2:74441875-74442022 | Common:2; Rare:26 | ||||
| chr2:74529665-74529997 | Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:84459205-84459593 | Common:3; Rare:99; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:85538916-85539168 | Common:1; Rare:89 | ||||
| chr2:85561432-85561612 | Rare:62; Clinvar:4 | ||||
| chr2:85595555-85595764 | Common:2; Rare:66 | ||||
| chr2:85612030-85612107 | Rare:20 |