| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:172750356-172750806 | Common:4; Rare:102 | ||||
| chr3:172750893-172751030 | Rare:42 | ||||
| chr3:179604620-179604848 | Common:2; Rare:84 | ||||
| chr3:180602020-180602235 | Common:1; Rare:70 | ||||
| chr3:180912557-180912700 | Rare:55 | ||||
| chr3:180989652-180989827 | Rare:74; Clinvar:1 | ||||
| chr3:181711736-181711977 | Rare:76 | ||||
| chr3:182793393-182793635 | Common:3; Rare:54 | ||||
| chr3:183099444-183099742 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:184017868-184018103 | Common:1; Rare:73 | ||||
| chr3:184135242-184135401 | Common:2; Rare:42; Clinvar:2 | ||||
| chr3:184185883-184186210 | Common:4; Rare:120 | ||||
| chr3:184248875-184248997 | Rare:69; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249459-184249800 | Common:1; Rare:103 | ||||
| chr3:184298947-184299364 | Common:5; Rare:128 |