| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61429929-61430158 | Common:1; Rare:104; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:61792573-61792955 | Common:5; Rare:102 | ||||
| chr11:62601228-62601336 | Rare:28 | ||||
| chr11:62665143-62665317 | Common:4; Rare:80 | ||||
| chr11:62855878-62856116 | Rare:93 | ||||
| chr11:64226141-64226318 | Common:2; Rare:49 | ||||
| chr11:64284630-64284843 | Common:1; Rare:101 | ||||
| chr11:64318038-64318293 | Rare:113 | ||||
| chr11:65014032-65014228 | Rare:49 | ||||
| chr11:65084041-65084272 | Common:1; Rare:70 | ||||
| chr11:65570366-65570510 | Rare:63 | ||||
| chr11:65662895-65663010 | Common:1; Rare:31 | ||||
| chr11:66002128-66002528 | Common:3; Rare:108; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66347630-66347826 | Common:5; Rare:50 | ||||
| chr11:66480239-66480448 | Common:1; Rare:55 |