| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65900243-65900403 | Common:4; Rare:38 | ||||
| chr11:65900405-65900492 | Rare:12 | ||||
| chr11:65920344-65920647 | Rare:103 | ||||
| chr11:66002087-66002836 | Common:4; Rare:214; Clinvar:8; Clinvar (benign):3 | ||||
| chr11:66268367-66268682 | Common:3; Rare:95 | ||||
| chr11:66344994-66345150 | Common:1; Rare:44 | ||||
| chr11:66480239-66480450 | Common:1; Rare:56 | ||||
| chr11:66593081-66593209 | Common:1; Rare:45 | ||||
| chr11:66616379-66616646 | Common:1; Rare:78 | ||||
| chr11:66638393-66638751 | Common:4; Rare:156 | ||||
| chr11:66677791-66678072 | Common:1; Rare:101 | ||||
| chr11:66744650-66744859 | Common:3; Rare:88 | ||||
| chr11:67353294-67353389 | Rare:28 | ||||
| chr11:67353443-67353692 | Common:1; Rare:62 | ||||
| chr11:67401741-67402075 | Common:3; Rare:123 |