| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71129812-71129908 | Rare:19 | ||||
| chr2:71130215-71130662 | Common:6; Rare:124; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071703-73071841 | Common:2; Rare:53 | ||||
| chr2:73233200-73233468 | Common:1; Rare:72 | ||||
| chr2:73234189-73234361 | Common:2; Rare:51 | ||||
| chr2:73828804-73829054 | Common:2; Rare:60 | ||||
| chr2:73926696-73926934 | Common:2; Rare:114; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147862-74148079 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178756-74179022 | Common:2; Rare:67 | ||||
| chr2:74421571-74421781 | Rare:71 | ||||
| chr2:74441854-74442063 | Common:2; Rare:45 | ||||
| chr2:74465371-74465455 | Common:1; Rare:20 | ||||
| chr2:74483000-74483120 | Rare:53 | ||||
| chr2:74527301-74527572 | Rare:81 | ||||
| chr2:74529659-74530006 | Rare:105; Clinvar:3; Clinvar (benign):1 |