| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70900319-70900714 | Common:8; Rare:120 | ||||
| chr2:70994779-70995080 | Common:4; Rare:93 | ||||
| chr2:71068526-71068672 | Rare:71 | ||||
| chr2:71130146-71130805 | Common:7; Rare:212; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276428-71276651 | Rare:86 | ||||
| chr2:73071701-73071888 | Common:2; Rare:72 | ||||
| chr2:73214178-73214279 | Common:1; Rare:36 | ||||
| chr2:73233195-73233496 | Common:1; Rare:87 | ||||
| chr2:73234193-73234368 | Common:2; Rare:55 | ||||
| chr2:73385580-73386090 | Common:4; Rare:231; Clinvar:17; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73386117-73386327 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:73737260-73737596 | Common:3; Rare:114 | ||||
| chr2:73828793-73829047 | Common:1; Rare:60 | ||||
| chr2:73926701-73926989 | Common:2; Rare:139; Clinvar:9; Clinvar (benign):3 | ||||
| chr2:74002558-74002730 | Common:2; Rare:70 |