| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69829501-69829735 | Common:1; Rare:96 | ||||
| chr2:70257935-70258165 | Common:1; Rare:75 | ||||
| chr2:70293659-70293841 | Common:2; Rare:62 | ||||
| chr2:71068526-71068678 | Rare:73 | ||||
| chr2:71130215-71130662 | Common:6; Rare:124; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73233200-73233494 | Common:1; Rare:84 | ||||
| chr2:73828821-73829020 | Common:1; Rare:46 | ||||
| chr2:74147862-74148111 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178804-74179066 | Common:4; Rare:81 | ||||
| chr2:74421639-74421767 | Rare:42 | ||||
| chr2:74454865-74455138 | Rare:75 | ||||
| chr2:74472419-74472703 | Common:4; Rare:128 | ||||
| chr2:74482949-74483095 | Common:1; Rare:51 | ||||
| chr2:74529665-74529788 | Rare:50; Clinvar:1 | ||||
| chr2:74530518-74530629 | Common:1; Rare:37; Clinvar:2 |