| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67353294-67353310 | Rare:6 | ||||
| chr11:67353323-67353370 | Rare:11 | ||||
| chr11:67353443-67353766 | Common:2; Rare:78 | ||||
| chr11:67373583-67373794 | Rare:41 | ||||
| chr11:67401768-67402075 | Common:3; Rare:113 | ||||
| chr11:67428394-67428545 | Rare:63 | ||||
| chr11:67469212-67469407 | Common:1; Rare:63 | ||||
| chr11:67482936-67483161 | Rare:52; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508038-67508216 | Common:1; Rare:55 | ||||
| chr11:67508627-67508751 | Common:2; Rare:41 | ||||
| chr11:67583656-67583866 | Common:1; Rare:74 | ||||
| chr11:68010130-68010371 | Common:1; Rare:62 | ||||
| chr11:68030380-68030764 | Common:3; Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68030891-68030959 | Common:5; Rare:27 | ||||
| chr11:68038915-68039101 | Rare:54; Clinvar:1 |