| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61144916-61145192 | Common:3; Rare:89 | ||||
| chr2:61177158-61177526 | Common:6; Rare:146 | ||||
| chr2:61470664-61470985 | Rare:109 | ||||
| chr2:61471257-61471387 | Common:2; Rare:47 | ||||
| chr2:61536466-61536767 | Common:2; Rare:86 | ||||
| chr2:61854000-61854113 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888487-61888748 | Common:2; Rare:109 | ||||
| chr2:61905551-61905724 | Rare:74 | ||||
| chr2:62506146-62506342 | Common:1; Rare:78 | ||||
| chr2:63588207-63588557 | Common:1; Rare:112; Clinvar:6 | ||||
| chr2:63588592-63589187 | Common:1; Rare:192; Clinvar (benign):1 | ||||
| chr2:63827821-63827984 | Rare:23 | ||||
| chr2:63840813-63841204 | Common:3; Rare:111 | ||||
| chr2:63841614-63841944 | Common:2; Rare:110 | ||||
| chr2:63842252-63842442 | Rare:56 |