| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:711403-711507 | Rare:15 | ||||
| chr6:868319-868483 | Common:1; Rare:32 | ||||
| chr6:1077016-1077275 | Common:3; Rare:58 | ||||
| chr6:1313868-1314110 | Common:1; Rare:57 | ||||
| chr6:1389086-1389125 | Rare:10 | ||||
| chr6:1389141-1389242 | Rare:33 | ||||
| chr6:1848359-1848673 | Common:3; Rare:47 | ||||
| chr6:2225781-2225861 | Rare:9 | ||||
| chr6:2272628-2272842 | Common:2; Rare:29 | ||||
| chr6:2389234-2389391 | Common:3; Rare:24 | ||||
| chr6:2777638-2777766 | Common:3; Rare:26 | ||||
| chr6:2836109-2836379 | Common:3; Rare:61 | ||||
| chr6:2990735-2990804 | Common:1; Rare:15 | ||||
| chr6:3155618-3155882 | Common:2; Rare:56; Clinvar (benign):3 | ||||
| chr6:3314940-3315181 | Common:2; Rare:51 |