| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43575914-43576339 | Common:2; Rare:149; Clinvar:10 | ||||
| chr6:43622617-43622937 | Common:1; Rare:72 | ||||
| chr6:43627327-43627492 | Rare:20 | ||||
| chr6:43629162-43629495 | Common:2; Rare:94 | ||||
| chr6:43770670-43770782 | Rare:32 | ||||
| chr6:44127324-44127682 | Common:4; Rare:103 | ||||
| chr6:44247013-44247216 | Common:2; Rare:93 | ||||
| chr6:44247982-44248174 | Common:4; Rare:62 | ||||
| chr6:45377452-45377520 | Common:2; Rare:24 | ||||
| chr6:45377774-45378183 | Common:2; Rare:129 | ||||
| chr6:46652715-46652985 | Rare:69 | ||||
| chr6:47477591-47477811 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:47478071-47478241 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:47698635-47698776 | Rare:33 | ||||
| chr6:49463180-49463439 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 |