| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73892706-73893072 | Common:3; Rare:68 | ||||
| chr2:74147862-74148140 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178800-74179066 | Common:4; Rare:83 | ||||
| chr2:74421639-74421762 | Rare:40 | ||||
| chr2:74440407-74440578 | Rare:44 | ||||
| chr2:74440582-74440756 | Rare:41 | ||||
| chr2:74441886-74442053 | Common:2; Rare:28 | ||||
| chr2:74458113-74458498 | Common:1; Rare:116 | ||||
| chr2:74459691-74459915 | Rare:76 | ||||
| chr2:74465336-74465439 | Rare:27; Clinvar:1 | ||||
| chr2:74472363-74472550 | Common:2; Rare:86 | ||||
| chr2:74482904-74483365 | Common:2; Rare:176 | ||||
| chr2:74503307-74503454 | Rare:36 | ||||
| chr2:74507282-74507504 | Rare:60 | ||||
| chr2:74529607-74530030 | Rare:139; Clinvar:4; Clinvar (benign):1 |