| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:70977641-70978024 | Rare:132; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:71065552-71065595 | Common:1; Rare:9 | ||||
| chr3:71130531-71130692 | Common:1; Rare:64; Clinvar:2 | ||||
| chr3:71130932-71131105 | Rare:32 | ||||
| chr3:71245013-71245287 | Common:1; Rare:54 | ||||
| chr3:71581871-71582142 | Common:1; Rare:61 | ||||
| chr3:71582155-71582392 | Rare:74 | ||||
| chr3:71754767-71754815 | Rare:5 | ||||
| chr3:73624106-73624477 | Common:6; Rare:114 | ||||
| chr3:81761504-81761746 | Common:8; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:86991063-86991361 | Common:1; Rare:75 | ||||
| chr3:87227245-87227482 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058435-88058735 | Common:1; Rare:97 | ||||
| chr3:88058923-88059322 | Common:3; Rare:152 | ||||
| chr3:88149618-88149733 | Rare:25 |