| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44246890-44247193 | Common:4; Rare:129 | ||||
| chr6:44247749-44248001 | Common:2; Rare:85 | ||||
| chr6:44342550-44342674 | Rare:34 | ||||
| chr6:44387439-44387810 | Common:4; Rare:102 | ||||
| chr6:45377628-45377730 | Common:1; Rare:43 | ||||
| chr6:45377866-45378198 | Common:2; Rare:116 | ||||
| chr6:46129753-46130180 | Common:5; Rare:133 | ||||
| chr6:46170838-46171140 | Common:2; Rare:78 | ||||
| chr6:46652803-46653048 | Rare:60 | ||||
| chr6:48068552-48068951 | Common:4; Rare:123 | ||||
| chr6:49463137-49463430 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:52284709-52285107 | Common:3; Rare:126 | ||||
| chr6:52420231-52420398 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52671032-52671398 | Rare:79 | ||||
| chr6:52995259-52995822 | Common:4; Rare:230 |