| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67464507-67464840 | Common:1; Rare:165 | ||||
| chr11:67469205-67469384 | Common:1; Rare:59 | ||||
| chr11:67482913-67483171 | Rare:57; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508050-67508353 | Common:1; Rare:73 | ||||
| chr11:67608294-67608541 | Rare:76; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:68003992-68004269 | Common:2; Rare:80 | ||||
| chr11:68030380-68030744 | Common:3; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038904-68039101 | Rare:58; Clinvar:1 | ||||
| chr11:68213579-68213924 | Common:1; Rare:201 | ||||
| chr11:68271871-68272265 | Common:2; Rare:162 | ||||
| chr11:68839335-68839496 | Common:1; Rare:41 | ||||
| chr11:68903784-68903955 | Common:5; Rare:82; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:69013208-69013477 | Common:2; Rare:77 | ||||
| chr11:69640990-69641267 | Common:1; Rare:61 | ||||
| chr11:69675300-69675541 | Common:1; Rare:68 |