| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67650184-67650374 | Common:3; Rare:40 | ||||
| chr11:67650583-67650708 | Common:1; Rare:30 | ||||
| chr11:67650933-67651275 | Common:4; Rare:69 | ||||
| chr11:68003464-68003801 | Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68004007-68004215 | Common:1; Rare:63 | ||||
| chr11:68030335-68030774 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68030834-68030995 | Common:6; Rare:60 | ||||
| chr11:68031243-68031379 | Rare:27 | ||||
| chr11:68038858-68039151 | Common:1; Rare:85; Clinvar:1 | ||||
| chr11:68039387-68039426 | Rare:5 | ||||
| chr11:68120676-68120897 | Rare:68 | ||||
| chr11:68121280-68121715 | Common:6; Rare:166 | ||||
| chr11:68121803-68121861 | Rare:11 | ||||
| chr11:68212684-68212917 | Rare:78 | ||||
| chr11:68213508-68213626 | Rare:65 |