| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67303343-67303557 | Rare:55 | ||||
| chr11:67353487-67353607 | Rare:32 | ||||
| chr11:67401778-67402075 | Common:3; Rare:111 | ||||
| chr11:67428257-67428531 | Rare:91 | ||||
| chr11:67443451-67443710 | Common:2; Rare:87 | ||||
| chr11:67482936-67483171 | Rare:53; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:68030367-68030733 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271895-68272134 | Common:2; Rare:100 | ||||
| chr11:68460223-68460390 | Common:3; Rare:62 | ||||
| chr11:68903770-68903943 | Common:4; Rare:81; Clinvar (benign):6 | ||||
| chr11:69640972-69641234 | Common:1; Rare:53 | ||||
| chr11:69675309-69675472 | Rare:43 | ||||
| chr11:70398421-70398596 | Common:2; Rare:63 | ||||
| chr11:70826706-70826816 | Rare:23 | ||||
| chr11:71448327-71448711 | Common:4; Rare:102; Clinvar:3; Clinvar (benign):1 |