| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66268404-66268676 | Common:3; Rare:78 | ||||
| chr11:66288962-66289393 | Common:2; Rare:110 | ||||
| chr11:66345030-66345242 | Common:1; Rare:61 | ||||
| chr11:66347586-66347879 | Common:5; Rare:68 | ||||
| chr11:66480226-66480462 | Common:1; Rare:64 | ||||
| chr11:66510561-66510696 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66593042-66593218 | Common:1; Rare:64 | ||||
| chr11:66616356-66616657 | Common:1; Rare:93 | ||||
| chr11:66638392-66638740 | Common:4; Rare:156 | ||||
| chr11:66677769-66678128 | Common:1; Rare:126 | ||||
| chr11:66744671-66744859 | Common:2; Rare:78 | ||||
| chr11:66958350-66958673 | Common:3; Rare:101; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:67056762-67056894 | Common:1; Rare:41 | ||||
| chr11:67239819-67240146 | Rare:71 | ||||
| chr11:67353451-67353830 | Common:2; Rare:93 |