| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:58046620-58046875 | Common:2; Rare:79 | ||||
| chr2:58241316-58241431 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:61017425-61017753 | Common:1; Rare:98; Clinvar:2 | ||||
| chr2:61144901-61145169 | Common:3; Rare:91 | ||||
| chr2:61471167-61471379 | Common:2; Rare:81 | ||||
| chr2:61538219-61538427 | Common:1; Rare:50 | ||||
| chr2:61854037-61854093 | Common:2; Rare:27; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888406-61888723 | Common:1; Rare:145 | ||||
| chr2:63588446-63588566 | Common:1; Rare:22; Clinvar:2 | ||||
| chr2:63588604-63589031 | Common:1; Rare:132; Clinvar (benign):1 | ||||
| chr2:63840822-63841142 | Common:1; Rare:88 | ||||
| chr2:63841646-63841978 | Common:2; Rare:109 | ||||
| chr2:64018985-64019146 | Common:1; Rare:48 | ||||
| chr2:65227578-65227941 | Rare:101 | ||||
| chr2:65432319-65432468 | Common:1; Rare:32 |