| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:65056133-65056473 | Common:2; Rare:120 | ||||
| chr2:65130162-65130607 | Common:1; Rare:118 | ||||
| chr2:65227582-65227955 | Rare:100 | ||||
| chr2:66434802-66435179 | Common:1; Rare:90 | ||||
| chr2:68062958-68063119 | Common:2; Rare:51 | ||||
| chr2:68157456-68157955 | Common:2; Rare:256 | ||||
| chr2:68252167-68252331 | Common:2; Rare:50 | ||||
| chr2:68252483-68252879 | Common:3; Rare:125 | ||||
| chr2:68319888-68320070 | Rare:48 | ||||
| chr2:68467248-68467738 | Common:2; Rare:134 | ||||
| chr2:69012969-69013244 | Common:10; Rare:71 | ||||
| chr2:69013273-69013467 | Common:1; Rare:42 | ||||
| chr2:69387103-69387429 | Common:1; Rare:95; Clinvar:3 | ||||
| chr2:69437409-69437551 | Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:69437590-69437703 | Rare:52; Clinvar:3 |