| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67482970-67483250 | Rare:74; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr11:67507804-67508300 | Common:1; Rare:140 | ||||
| chr11:67508632-67508780 | Common:3; Rare:54 | ||||
| chr11:67583442-67583742 | Common:7; Rare:63 | ||||
| chr11:67611081-67611569 | Common:3; Rare:155; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67612092-67612417 | Common:4; Rare:124; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:68010238-68010355 | Common:1; Rare:31 | ||||
| chr11:68030355-68030768 | Common:3; Rare:115; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68121377-68121648 | Common:1; Rare:89 | ||||
| chr11:68271910-68272108 | Common:2; Rare:86 | ||||
| chr11:68460560-68460817 | Common:3; Rare:88 | ||||
| chr11:68841819-68841916 | Rare:33 | ||||
| chr11:68903725-68903933 | Common:4; Rare:91; Clinvar (benign):6 | ||||
| chr11:69640969-69641290 | Common:1; Rare:74 | ||||
| chr11:69641329-69641508 | Rare:47 |