| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1759409-1759640 | Common:3; Rare:70; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr11:1760864-1761132 | Rare:59 | ||||
| chr11:1762411-1762661 | Common:3; Rare:64 | ||||
| chr11:1763792-1764002 | Rare:75; Clinvar:10; Clinvar (benign):8 | ||||
| chr11:1863051-1863414 | Common:3; Rare:79 | ||||
| chr11:1863529-1863569 | Rare:8 | ||||
| chr11:1864003-1864192 | Rare:40 | ||||
| chr11:1864782-1865249 | Common:3; Rare:101 | ||||
| chr11:1868501-1869181 | Common:3; Rare:142 | ||||
| chr11:1869405-1869672 | Common:8; Rare:67 | ||||
| chr11:1870404-1870618 | Common:1; Rare:52 | ||||
| chr11:1870682-1870948 | Common:4; Rare:59 | ||||
| chr11:1871152-1871401 | Common:3; Rare:69 | ||||
| chr11:1871458-1871585 | Rare:30 | ||||
| chr11:2138236-2138538 | Common:1; Rare:61 |