| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70768070-70768451 | Common:5; Rare:76 | ||||
| chr2:70978578-70978648 | Rare:27 | ||||
| chr2:70994786-70995063 | Common:4; Rare:86 | ||||
| chr2:71068534-71068672 | Rare:64 | ||||
| chr2:71130225-71130677 | Common:6; Rare:129; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73214190-73214335 | Common:1; Rare:64 | ||||
| chr2:73233200-73233468 | Common:1; Rare:72 | ||||
| chr2:73234219-73234356 | Common:1; Rare:40 | ||||
| chr2:73385581-73386099 | Common:4; Rare:236; Clinvar:18; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73737266-73737589 | Common:3; Rare:107 | ||||
| chr2:73828804-73829029 | Common:1; Rare:53 | ||||
| chr2:74002580-74002705 | Common:2; Rare:49 | ||||
| chr2:74147866-74148062 | Common:1; Rare:53; Clinvar:2 | ||||
| chr2:74374615-74374803 | Rare:44 | ||||
| chr2:74391792-74392143 | Common:2; Rare:165 |