| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66677772-66678024 | Common:1; Rare:100 | ||||
| chr11:66744650-66744849 | Common:3; Rare:84 | ||||
| chr11:66843320-66843537 | Common:6; Rare:110 | ||||
| chr11:66907857-66908065 | Common:2; Rare:29 | ||||
| chr11:66958532-66958852 | Common:5; Rare:83 | ||||
| chr11:67121041-67121319 | Common:1; Rare:53 | ||||
| chr11:67303356-67303582 | Rare:58 | ||||
| chr11:67317758-67317877 | Rare:22 | ||||
| chr11:67353292-67353340 | Rare:16 | ||||
| chr11:67353460-67353717 | Common:1; Rare:61 | ||||
| chr11:67401754-67402075 | Common:3; Rare:116 | ||||
| chr11:67428394-67428537 | Rare:57 | ||||
| chr11:67443435-67443553 | Common:1; Rare:36 | ||||
| chr11:67482936-67483154 | Rare:50; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67508635-67508761 | Common:2; Rare:45 |