| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017177-61017749 | Common:4; Rare:163; Clinvar:2 | ||||
| chr2:61144921-61145187 | Common:3; Rare:87 | ||||
| chr2:61471071-61471386 | Common:2; Rare:122 | ||||
| chr2:61492096-61492695 | Common:2; Rare:101; Clinvar (pathogenic):1 | ||||
| chr2:61537663-61537712 | Rare:10 | ||||
| chr2:61537746-61537952 | Common:1; Rare:60 | ||||
| chr2:61854016-61854224 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888411-61888700 | Common:1; Rare:134 | ||||
| chr2:63588604-63589031 | Common:1; Rare:132; Clinvar (benign):1 | ||||
| chr2:63840846-63841141 | Common:1; Rare:80 | ||||
| chr2:63841624-63841990 | Common:2; Rare:117 | ||||
| chr2:64524102-64524370 | Common:3; Rare:76 | ||||
| chr2:64653911-64654078 | Common:1; Rare:62 | ||||
| chr2:64988328-64988519 | Common:1; Rare:38 | ||||
| chr2:65056144-65056462 | Common:2; Rare:110 |