| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:695731-695818 | Rare:29 | ||||
| chr11:706516-706646 | Rare:21 | ||||
| chr11:764095-764412 | Rare:94; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:777465-777621 | Common:1; Rare:68 | ||||
| chr11:809516-809627 | Common:2; Rare:30 | ||||
| chr11:809808-810038 | Common:2; Rare:104 | ||||
| chr11:832782-833026 | Common:7; Rare:77 | ||||
| chr11:842413-842978 | Common:8; Rare:231 | ||||
| chr11:843964-844159 | Common:1; Rare:47 | ||||
| chr11:844206-844448 | Common:3; Rare:71 | ||||
| chr11:1223035-1223111 | Rare:24 | ||||
| chr11:1259900-1259965 | Common:1; Rare:15 | ||||
| chr11:1309535-1309780 | Common:2; Rare:107 | ||||
| chr11:1481494-1481826 | Common:9; Rare:72 | ||||
| chr11:1486651-1487059 | Common:2; Rare:72 |