| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70673123-70673274 | Common:1; Rare:43 | ||||
| chr2:71068538-71068678 | Rare:62 | ||||
| chr2:71130146-71130698 | Common:7; Rare:168; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71130718-71130790 | Rare:30 | ||||
| chr2:71417972-71418087 | Rare:27 | ||||
| chr2:71466546-71466709 | Common:3; Rare:42 | ||||
| chr2:73071701-73071864 | Common:2; Rare:61 | ||||
| chr2:73214134-73214306 | Common:1; Rare:61 | ||||
| chr2:73233195-73233468 | Common:1; Rare:75 | ||||
| chr2:73234182-73234370 | Common:2; Rare:57 | ||||
| chr2:73385644-73386070 | Common:4; Rare:198; Clinvar:16; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr2:73737266-73737582 | Common:3; Rare:104 | ||||
| chr2:73828793-73829037 | Common:1; Rare:55 | ||||
| chr2:73926742-73926913 | Common:2; Rare:86; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:74147836-74148150 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):1 |