| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71068526-71068711 | Rare:84 | ||||
| chr2:71130215-71130698 | Common:7; Rare:141; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276422-71276680 | Rare:101 | ||||
| chr2:72825879-72826079 | Rare:68 | ||||
| chr2:72887210-72887427 | Common:2; Rare:66; Clinvar (benign):1 | ||||
| chr2:73071692-73071868 | Common:2; Rare:70 | ||||
| chr2:73214199-73214398 | Common:2; Rare:87 | ||||
| chr2:73214481-73214674 | Common:2; Rare:66 | ||||
| chr2:73233174-73233504 | Common:2; Rare:98 | ||||
| chr2:73234189-73234361 | Common:2; Rare:51 | ||||
| chr2:73284209-73284524 | Common:1; Rare:78 | ||||
| chr2:73284776-73284855 | Rare:15 | ||||
| chr2:73385688-73386076 | Common:4; Rare:187; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73386182-73386339 | Common:1; Rare:58; Clinvar (benign):3 | ||||
| chr2:73737250-73737498 | Common:2; Rare:81 |