| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67353451-67353790 | Common:2; Rare:87 | ||||
| chr11:67401768-67402078 | Common:3; Rare:114 | ||||
| chr11:67428307-67428533 | Rare:78 | ||||
| chr11:67443458-67443778 | Common:2; Rare:104 | ||||
| chr11:67469229-67469407 | Common:1; Rare:52 | ||||
| chr11:67482936-67483154 | Rare:50; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67508126-67508396 | Common:1; Rare:60 | ||||
| chr11:68030380-68030736 | Common:3; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68213558-68213893 | Rare:194 | ||||
| chr11:68271895-68272139 | Common:2; Rare:102 | ||||
| chr11:68460222-68460335 | Common:2; Rare:54 | ||||
| chr11:68903784-68903955 | Common:5; Rare:82; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:69048735-69048953 | Common:5; Rare:75 | ||||
| chr11:69640972-69641215 | Rare:52 | ||||
| chr11:69675289-69675477 | Rare:55 |