| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71130194-71130676 | Common:6; Rare:140; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276422-71276623 | Rare:75 | ||||
| chr2:71453478-71453691 | Common:1; Rare:42 | ||||
| chr2:73071707-73071843 | Common:2; Rare:50 | ||||
| chr2:73214172-73214279 | Common:1; Rare:38 | ||||
| chr2:73233200-73233468 | Common:1; Rare:72 | ||||
| chr2:73234225-73234368 | Common:1; Rare:46 | ||||
| chr2:73737304-73737675 | Common:3; Rare:118 | ||||
| chr2:73828821-73829024 | Common:1; Rare:47 | ||||
| chr2:73892744-73893072 | Common:3; Rare:57 | ||||
| chr2:74147870-74148150 | Common:2; Rare:68; Clinvar:2 | ||||
| chr2:74198430-74198637 | Rare:80 | ||||
| chr2:74421582-74421779 | Rare:68 | ||||
| chr2:74458157-74458495 | Common:1; Rare:104 | ||||
| chr2:74459667-74459941 | Rare:96 |