| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013838-43014280 | Common:2; Rare:109 | ||||
| chr6:43477483-43477597 | Rare:25 | ||||
| chr6:43516891-43517115 | Common:4; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575952-43576190 | Rare:95; Clinvar:4 | ||||
| chr6:43635697-43635867 | Common:2; Rare:35 | ||||
| chr6:43770088-43770230 | Common:2; Rare:43 | ||||
| chr6:44127351-44127639 | Common:4; Rare:81 | ||||
| chr6:44387439-44387747 | Common:4; Rare:81 | ||||
| chr6:45377788-45378183 | Common:2; Rare:126 | ||||
| chr6:46129823-46130096 | Common:5; Rare:89 | ||||
| chr6:47477602-47478015 | Common:2; Rare:108; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:47478067-47478247 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:49463241-49463417 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr6:52420122-52420392 | Common:3; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995266-52995808 | Common:4; Rare:227 |