| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:65227603-65227857 | Rare:67 | ||||
| chr2:68157444-68157949 | Common:2; Rare:257 | ||||
| chr2:69387178-69387419 | Rare:70; Clinvar:2 | ||||
| chr2:69643641-69643794 | Rare:58 | ||||
| chr2:69829517-69829686 | Rare:65 | ||||
| chr2:70293655-70293821 | Common:2; Rare:60 | ||||
| chr2:71068539-71068672 | Rare:59 | ||||
| chr2:71130225-71130327 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276430-71276599 | Rare:54 | ||||
| chr2:73071701-73071848 | Common:2; Rare:57 | ||||
| chr2:73385647-73385866 | Common:2; Rare:86; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147870-74148048 | Common:1; Rare:46; Clinvar:2 | ||||
| chr2:74178834-74179009 | Common:1; Rare:47 | ||||
| chr2:74421639-74421759 | Rare:39 | ||||
| chr2:74454881-74455128 | Rare:71 |