| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:69796546-69796662 | Common:1; Rare:23 | ||||
| chr6:69796847-69797135 | Common:1; Rare:91; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:69866543-69866615 | Rare:14 | ||||
| chr6:70413195-70413603 | Common:2; Rare:118 | ||||
| chr6:70566843-70567000 | Common:2; Rare:62 | ||||
| chr6:70667696-70668104 | Common:5; Rare:153 | ||||
| chr6:70955852-70956178 | Common:1; Rare:115 | ||||
| chr6:71288059-71288447 | Common:1; Rare:82 | ||||
| chr6:71886433-71887169 | Common:3; Rare:220; Clinvar:3; Clinvar (benign):4 | ||||
| chr6:73263146-73263304 | Common:5; Rare:44 | ||||
| chr6:73309707-73309804 | Rare:26 | ||||
| chr6:73310134-73310408 | Common:3; Rare:62 | ||||
| chr6:73461437-73461807 | Common:2; Rare:75 | ||||
| chr6:73520998-73521414 | Common:3; Rare:110 | ||||
| chr6:73521519-73521668 | Rare:42 |