| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43516719-43517133 | Common:6; Rare:150; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575882-43576186 | Common:1; Rare:121; Clinvar:4 | ||||
| chr6:43627306-43627491 | Rare:25 | ||||
| chr6:43629010-43629122 | Common:1; Rare:36 | ||||
| chr6:43770087-43770555 | Common:5; Rare:111 | ||||
| chr6:43770610-43770872 | Common:2; Rare:80; Clinvar:1 | ||||
| chr6:43777555-43778214 | Common:1; Rare:131 | ||||
| chr6:44126772-44126933 | Rare:43 | ||||
| chr6:44127275-44127681 | Common:4; Rare:113 | ||||
| chr6:44257455-44257679 | Rare:68 | ||||
| chr6:45377447-45377548 | Common:2; Rare:36 | ||||
| chr6:45377559-45377593 | Rare:6 | ||||
| chr6:45377594-45377746 | Common:3; Rare:60 | ||||
| chr6:45377777-45378184 | Common:2; Rare:129 | ||||
| chr6:45422181-45422591 | Common:3; Rare:111 |