| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41921109-41921275 | Rare:43 | ||||
| chr6:42929240-42929561 | Common:3; Rare:87 | ||||
| chr6:42984337-42984619 | Rare:66 | ||||
| chr6:43013863-43014270 | Common:2; Rare:90 | ||||
| chr6:43477390-43477582 | Rare:34 | ||||
| chr6:43516893-43517106 | Common:3; Rare:84; Clinvar:2 | ||||
| chr6:43770095-43770229 | Common:1; Rare:41 | ||||
| chr6:44127357-44127657 | Common:4; Rare:88 | ||||
| chr6:44387410-44387749 | Common:4; Rare:85 | ||||
| chr6:47478070-47478232 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:49463191-49463433 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420238-52420385 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52995275-52995807 | Common:4; Rare:224 | ||||
| chr6:57172550-57172764 | Common:1; Rare:70 | ||||
| chr6:73519883-73520241 | Common:1; Rare:133 |