| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71453881-71454032 | Rare:42; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:71611048-71611321 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:73071266-73071479 | Common:1; Rare:76 | ||||
| chr2:73071694-73071848 | Common:2; Rare:61 | ||||
| chr2:73112860-73113141 | Common:4; Rare:75 | ||||
| chr2:73214166-73214311 | Common:1; Rare:57 | ||||
| chr2:73233183-73233499 | Common:1; Rare:91 | ||||
| chr2:73234244-73234368 | Common:1; Rare:43 | ||||
| chr2:73234544-73234645 | Rare:37 | ||||
| chr2:73284287-73284531 | Common:1; Rare:61 | ||||
| chr2:73284783-73284861 | Rare:12 | ||||
| chr2:73385647-73386081 | Common:4; Rare:203; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73386243-73386321 | Rare:31 | ||||
| chr2:73737220-73737498 | Common:2; Rare:88 | ||||
| chr2:73828804-73829047 | Common:1; Rare:59 |