| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71130703-71130794 | Rare:35 | ||||
| chr2:71276450-71276620 | Rare:58 | ||||
| chr2:73071707-73071848 | Common:2; Rare:52 | ||||
| chr2:73214146-73214279 | Common:1; Rare:44 | ||||
| chr2:73233200-73233473 | Common:1; Rare:76 | ||||
| chr2:73234214-73234368 | Common:2; Rare:49 | ||||
| chr2:73284775-73284894 | Rare:20 | ||||
| chr2:73385580-73386063 | Common:4; Rare:215; Clinvar:16; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr2:73386117-73386321 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:73737300-73737596 | Common:3; Rare:100 | ||||
| chr2:73828804-73829020 | Common:1; Rare:50 | ||||
| chr2:73926701-73926939 | Common:2; Rare:117; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147862-74148052 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178812-74179012 | Common:2; Rare:57 | ||||
| chr2:74198424-74198634 | Rare:81 |