| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67482913-67483154 | Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67583655-67583857 | Common:1; Rare:68 | ||||
| chr11:68010132-68010354 | Common:1; Rare:58 | ||||
| chr11:68030453-68030755 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039101 | Rare:54; Clinvar:1 | ||||
| chr11:68049601-68049698 | Rare:32; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr11:68213486-68213930 | Common:1; Rare:249 | ||||
| chr11:68271865-68272134 | Common:2; Rare:109 | ||||
| chr11:68460223-68460331 | Common:2; Rare:52 | ||||
| chr11:68460560-68460803 | Common:3; Rare:86 | ||||
| chr11:68839287-68839548 | Common:1; Rare:60 | ||||
| chr11:68903774-68903943 | Common:4; Rare:80; Clinvar (benign):6 | ||||
| chr11:69013191-69013276 | Common:1; Rare:17 | ||||
| chr11:69048701-69048970 | Common:5; Rare:91 | ||||
| chr11:69640990-69641235 | Common:1; Rare:51 |