| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:53348824-53349222 | Common:2; Rare:168 | ||||
| chr6:53545098-53545239 | Rare:40 | ||||
| chr6:53665688-53665929 | Common:1; Rare:50 | ||||
| chr6:56542779-56543159 | Common:3; Rare:68 | ||||
| chr6:57046413-57046759 | Rare:120 | ||||
| chr6:57172450-57172764 | Common:1; Rare:95 | ||||
| chr6:63572324-63572622 | Rare:111 | ||||
| chr6:63636063-63636132 | Rare:23 | ||||
| chr6:68635138-68635361 | Common:1; Rare:69 | ||||
| chr6:69796868-69797162 | Common:1; Rare:91; Clinvar:6; Clinvar (benign):2 | ||||
| chr6:70413176-70413595 | Common:2; Rare:126 | ||||
| chr6:70566798-70566958 | Common:1; Rare:52 | ||||
| chr6:70667707-70667970 | Common:2; Rare:91 | ||||
| chr6:71289012-71289159 | Common:1; Rare:53 | ||||
| chr6:73310152-73310327 | Common:1; Rare:39 |