| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71068534-71068678 | Rare:66 | ||||
| chr2:71130140-71130677 | Common:6; Rare:160; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71226960-71227422 | Common:2; Rare:111 | ||||
| chr2:71276421-71276707 | Rare:116 | ||||
| chr2:71453441-71453912 | Common:3; Rare:86 | ||||
| chr2:71466596-71466738 | Common:3; Rare:32 | ||||
| chr2:72144492-72144710 | Common:3; Rare:49 | ||||
| chr2:73071707-73071857 | Common:2; Rare:54 | ||||
| chr2:73214149-73214265 | Common:1; Rare:34 | ||||
| chr2:73233185-73233440 | Common:1; Rare:69 | ||||
| chr2:73234214-73234361 | Common:2; Rare:44 | ||||
| chr2:73385644-73386099 | Common:4; Rare:216; Clinvar:18; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73737295-73737505 | Common:3; Rare:67 | ||||
| chr2:73828801-73829029 | Common:1; Rare:53 | ||||
| chr2:74147849-74148157 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):1 |