| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:145814709-145814916 | Common:1; Rare:98 | ||||
| chr6:148342340-148342441 | Rare:19 | ||||
| chr6:148342900-148343221 | Common:1; Rare:122 | ||||
| chr6:149749529-149749796 | Rare:120 | ||||
| chr6:149941835-149942045 | Common:6; Rare:44 | ||||
| chr6:150866276-150866551 | Rare:115 | ||||
| chr6:151240234-151240416 | Common:1; Rare:49 | ||||
| chr6:151325475-151325780 | Common:2; Rare:72 | ||||
| chr6:151391509-151391828 | Common:3; Rare:86 | ||||
| chr6:151452032-151452540 | Common:4; Rare:177 | ||||
| chr6:152302056-152302221 | Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152983021-152983351 | Common:2; Rare:101 | ||||
| chr6:153002617-153002925 | Common:4; Rare:114 | ||||
| chr6:153131225-153131518 | Rare:133 | ||||
| chr6:155314456-155314655 | Common:2; Rare:74 |