| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66480239-66480455 | Common:1; Rare:58 | ||||
| chr11:66510554-66510696 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66593066-66593209 | Common:1; Rare:47 | ||||
| chr11:66616403-66616657 | Common:1; Rare:71 | ||||
| chr11:66638393-66638725 | Common:3; Rare:146 | ||||
| chr11:66677765-66678079 | Common:1; Rare:114 | ||||
| chr11:66729001-66729113 | Common:1; Rare:23 | ||||
| chr11:66744648-66744892 | Common:3; Rare:99 | ||||
| chr11:66958347-66958597 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:67303343-67303575 | Rare:60 | ||||
| chr11:67317752-67317881 | Rare:23 | ||||
| chr11:67353504-67353721 | Common:1; Rare:60 | ||||
| chr11:67401778-67402075 | Common:3; Rare:111 | ||||
| chr11:67428336-67428545 | Rare:75 | ||||
| chr11:67469228-67469349 | Rare:36 |