| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67469148-67469407 | Common:3; Rare:94 | ||||
| chr11:67508679-67508778 | Common:2; Rare:38 | ||||
| chr11:68030607-68030965 | Common:7; Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68036346-68036575 | Rare:87; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:68038909-68039083 | Rare:54; Clinvar:1 | ||||
| chr11:68271901-68272129 | Common:2; Rare:95 | ||||
| chr11:68903803-68903946 | Common:4; Rare:62; Clinvar (benign):6 | ||||
| chr11:69640840-69641310 | Common:1; Rare:108 | ||||
| chr11:70270500-70270747 | Common:2; Rare:100 | ||||
| chr11:70398350-70398617 | Common:2; Rare:96 | ||||
| chr11:70407298-70407597 | Common:2; Rare:83 | ||||
| chr11:71448328-71448681 | Common:4; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71453029-71453268 | Common:1; Rare:70 | ||||
| chr11:71928957-71929067 | Common:1; Rare:37 | ||||
| chr11:72040701-72040994 | Rare:63 |