| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43770610-43770802 | Common:2; Rare:52; Clinvar:1 | ||||
| chr6:44126803-44126933 | Rare:39 | ||||
| chr6:44127339-44127685 | Common:4; Rare:98 | ||||
| chr6:45422181-45422349 | Rare:41 | ||||
| chr6:46652708-46652985 | Rare:72 | ||||
| chr6:49463170-49463430 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52576919-52577331 | Common:7; Rare:148 | ||||
| chr6:52671040-52671174 | Rare:43 | ||||
| chr6:56542838-56543070 | Common:2; Rare:34 | ||||
| chr6:56843643-56843939 | Common:9; Rare:65 | ||||
| chr6:57046502-57046750 | Rare:87 | ||||
| chr6:57221422-57221580 | Rare:35 | ||||
| chr6:73263182-73263279 | Common:2; Rare:23 | ||||
| chr6:73520062-73520279 | Common:1; Rare:87 | ||||
| chr6:73695993-73696138 | Common:1; Rare:26 |