| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42984297-42984591 | Rare:70 | ||||
| chr6:43013846-43014321 | Common:2; Rare:114 | ||||
| chr6:43059820-43059910 | Rare:30 | ||||
| chr6:43516848-43517123 | Common:5; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575943-43576153 | Rare:78 | ||||
| chr6:43770620-43770795 | Common:1; Rare:48 | ||||
| chr6:44127348-44127652 | Common:4; Rare:90 | ||||
| chr6:45377788-45378166 | Common:2; Rare:121 | ||||
| chr6:46652839-46652945 | Rare:26 | ||||
| chr6:47478100-47478201 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:49463205-49463438 | Common:1; Rare:68; Clinvar (benign):1 | ||||
| chr6:52576885-52577307 | Common:7; Rare:151 | ||||
| chr6:73696109-73696210 | Rare:20 | ||||
| chr6:75284742-75285015 | Common:1; Rare:74 | ||||
| chr6:78867456-78867753 | Common:1; Rare:117 |