| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61470651-61470986 | Rare:112 | ||||
| chr2:61471257-61471387 | Common:2; Rare:47 | ||||
| chr2:61536745-61536771 | Rare:6 | ||||
| chr2:61854010-61854084 | Common:2; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888483-61888693 | Common:1; Rare:91 | ||||
| chr2:62506146-62506319 | Common:1; Rare:70 | ||||
| chr2:63588207-63588566 | Common:1; Rare:113; Clinvar:6 | ||||
| chr2:63588618-63589045 | Common:1; Rare:130; Clinvar (benign):1 | ||||
| chr2:63840822-63841184 | Common:3; Rare:97 | ||||
| chr2:63841614-63842145 | Common:3; Rare:150 | ||||
| chr2:64018991-64019187 | Common:1; Rare:53 | ||||
| chr2:64144291-64144683 | Common:4; Rare:111 | ||||
| chr2:64454001-64454224 | Rare:48 | ||||
| chr2:64653707-64654071 | Common:1; Rare:122 | ||||
| chr2:65056166-65056462 | Common:2; Rare:102 |