| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67630053-67630296 | Common:7; Rare:40 | ||||
| chr11:68030361-68030969 | Common:9; Rare:181; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68036308-68036474 | Rare:67; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr11:68120722-68120839 | Rare:37 | ||||
| chr11:68120853-68120971 | Rare:39 | ||||
| chr11:68121357-68121667 | Common:1; Rare:109 | ||||
| chr11:68271891-68272183 | Common:2; Rare:125 | ||||
| chr11:68312150-68312712 | Common:2; Rare:163; Clinvar (benign):1 | ||||
| chr11:68460223-68460507 | Common:3; Rare:92 | ||||
| chr11:68460543-68460826 | Common:3; Rare:98 | ||||
| chr11:68750613-68750922 | Common:2; Rare:62 | ||||
| chr11:68751391-68751578 | Common:1; Rare:40 | ||||
| chr11:68903718-68903930 | Common:4; Rare:90; Clinvar (benign):6 | ||||
| chr11:69013194-69013348 | Common:2; Rare:35 | ||||
| chr11:69013533-69013812 | Common:2; Rare:57 |