| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67583673-67583844 | Common:1; Rare:59 | ||||
| chr11:67611229-67611535 | Common:2; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:68030399-68030744 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68030891-68030970 | Common:5; Rare:30 | ||||
| chr11:68038925-68039078 | Rare:47; Clinvar:1 | ||||
| chr11:68121264-68121656 | Common:5; Rare:151 | ||||
| chr11:68213535-68213929 | Common:1; Rare:225 | ||||
| chr11:68271865-68272134 | Common:2; Rare:109 | ||||
| chr11:68460534-68460809 | Common:3; Rare:99 | ||||
| chr11:68773821-68773977 | Common:1; Rare:47 | ||||
| chr11:68903774-68903943 | Common:4; Rare:80; Clinvar (benign):6 | ||||
| chr11:68929972-68930130 | Rare:31 | ||||
| chr11:69048747-69048995 | Common:6; Rare:91 | ||||
| chr11:69640972-69641167 | Rare:40 | ||||
| chr11:69675289-69675503 | Rare:61 |