| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67056757-67056923 | Common:1; Rare:50 | ||||
| chr11:67303343-67303577 | Rare:61 | ||||
| chr11:67353493-67353811 | Common:2; Rare:87 | ||||
| chr11:67401780-67402069 | Common:3; Rare:109 | ||||
| chr11:67428394-67428531 | Rare:55 | ||||
| chr11:67443458-67443625 | Common:1; Rare:64 | ||||
| chr11:67469229-67469439 | Common:1; Rare:59 | ||||
| chr11:68030390-68030744 | Common:3; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271910-68272156 | Common:2; Rare:104 | ||||
| chr11:68903779-68903955 | Common:5; Rare:85; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:69641005-69641250 | Common:1; Rare:46 | ||||
| chr11:69675315-69675486 | Rare:47 | ||||
| chr11:70398421-70398596 | Common:2; Rare:63 | ||||
| chr11:71448347-71448673 | Common:4; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928930-71929061 | Common:1; Rare:44 |