| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65615714-65615835 | Rare:39 | ||||
| chr11:65662881-65663028 | Common:1; Rare:40 | ||||
| chr11:65900322-65900613 | Common:4; Rare:64 | ||||
| chr11:66002097-66002845 | Common:4; Rare:214; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:66289072-66289393 | Common:1; Rare:77 | ||||
| chr11:66347605-66347896 | Common:5; Rare:68 | ||||
| chr11:66480212-66480448 | Common:3; Rare:62 | ||||
| chr11:66616408-66616634 | Common:1; Rare:58 | ||||
| chr11:66638393-66638757 | Common:4; Rare:158 | ||||
| chr11:66677775-66677972 | Common:1; Rare:77 | ||||
| chr11:66744652-66744848 | Common:3; Rare:82 | ||||
| chr11:67317769-67317877 | Rare:19 | ||||
| chr11:67353499-67353722 | Common:1; Rare:61 | ||||
| chr11:67401756-67402071 | Common:3; Rare:115 | ||||
| chr11:67443427-67443625 | Common:1; Rare:75 |