| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43575952-43576178 | Rare:88; Clinvar:4 | ||||
| chr6:43770063-43770287 | Common:4; Rare:61 | ||||
| chr6:43771024-43771233 | Rare:80 | ||||
| chr6:43771877-43771985 | Rare:20 | ||||
| chr6:43773378-43773575 | Common:2; Rare:34 | ||||
| chr6:44127325-44127671 | Common:4; Rare:100 | ||||
| chr6:44223485-44223637 | Common:1; Rare:53 | ||||
| chr6:44229440-44229737 | Rare:86 | ||||
| chr6:46129777-46130176 | Common:5; Rare:126 | ||||
| chr6:46491938-46492062 | Rare:20 | ||||
| chr6:46652718-46653013 | Rare:74 | ||||
| chr6:46921819-46922076 | Common:3; Rare:68 | ||||
| chr6:47477690-47478255 | Common:5; Rare:163; Clinvar:7; Clinvar (benign):7 | ||||
| chr6:49463167-49463412 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284709-52284805 | Common:1; Rare:45 |