| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:18155032-18155532 | Common:22; Rare:235; Clinvar:4 | ||||
| chr6:18263946-18264711 | Common:4; Rare:445 | ||||
| chr6:18387290-18387508 | Common:4; Rare:139 | ||||
| chr6:20212389-20212592 | Common:2; Rare:90 | ||||
| chr6:20401547-20402148 | Common:5; Rare:225 | ||||
| chr6:20402192-20402610 | Rare:268 | ||||
| chr6:20403363-20403843 | Common:2; Rare:163 | ||||
| chr6:20534379-20534763 | Common:4; Rare:157 | ||||
| chr6:24402777-24403016 | Common:5; Rare:121 | ||||
| chr6:24495070-24495790 | Common:6; Rare:226; Clinvar:21; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:24645651-24645948 | Common:5; Rare:48 | ||||
| chr6:24646030-24646245 | Common:1; Rare:63 | ||||
| chr6:24646165-24646303 | Common:2; Rare:44 | ||||
| chr6:24658710-24659745 | Common:10; Rare:288 | ||||
| chr6:24666716-24667255 | Common:8; Rare:420 |