| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:696221-696324 | Rare:17 | ||||
| chr11:725737-725816 | Rare:20 | ||||
| chr11:726365-726486 | Rare:45 | ||||
| chr11:726591-726617 | Rare:12 | ||||
| chr11:747171-747517 | Rare:127; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:776616-776786 | Common:2; Rare:35 | ||||
| chr11:777417-777691 | Common:2; Rare:124 | ||||
| chr11:796186-796447 | Rare:70; Clinvar:1 | ||||
| chr11:797339-797481 | Common:1; Rare:42 | ||||
| chr11:797563-797773 | Rare:58 | ||||
| chr11:797916-798061 | Common:1; Rare:40 | ||||
| chr11:805170-805576 | Common:8; Rare:135 | ||||
| chr11:809223-809338 | Common:2; Rare:28 | ||||
| chr11:809429-809671 | Common:3; Rare:69 | ||||
| chr11:809738-810044 | Common:2; Rare:132 |