| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61470651-61471052 | Common:1; Rare:132 | ||||
| chr2:61471078-61471387 | Common:2; Rare:119 | ||||
| chr2:61536538-61536775 | Common:1; Rare:71 | ||||
| chr2:61537063-61537152 | Rare:18 | ||||
| chr2:61538181-61538439 | Common:1; Rare:58 | ||||
| chr2:61854000-61854207 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888309-61888733 | Common:1; Rare:187 | ||||
| chr2:62506131-62506297 | Common:1; Rare:65 | ||||
| chr2:63588207-63588566 | Common:1; Rare:113; Clinvar:6 | ||||
| chr2:63588604-63589046 | Common:1; Rare:137; Clinvar (benign):1 | ||||
| chr2:63840813-63841192 | Common:3; Rare:107 | ||||
| chr2:63841614-63842108 | Common:2; Rare:137 | ||||
| chr2:64018981-64019187 | Common:1; Rare:54 | ||||
| chr2:64019395-64019483 | Rare:36 | ||||
| chr2:64524105-64524475 | Common:3; Rare:119 |