| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61362255-61362407 | Common:1; Rare:43; Clinvar:7 | ||||
| chr11:61392527-61392649 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429912-61430176 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):6 | ||||
| chr11:61792563-61792948 | Common:5; Rare:107 | ||||
| chr11:61816103-61816325 | Rare:58 | ||||
| chr11:61816545-61816599 | Rare:6 | ||||
| chr11:61816760-61817033 | Rare:73 | ||||
| chr11:61967311-61967806 | Common:3; Rare:185; Clinvar:4 | ||||
| chr11:62123731-62124073 | Common:7; Rare:91 | ||||
| chr11:62545566-62545987 | Common:1; Rare:95 | ||||
| chr11:62621949-62622234 | Common:2; Rare:87 | ||||
| chr11:62653262-62653504 | Common:1; Rare:72 | ||||
| chr11:62665139-62665418 | Common:5; Rare:134 | ||||
| chr11:62678866-62679186 | Rare:107 | ||||
| chr11:62706231-62706400 | Common:2; Rare:69; Clinvar (benign):4 |