| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42547663-42547851 | Rare:42 | ||||
| chr6:42548081-42548299 | Rare:34 | ||||
| chr6:42550406-42550554 | Rare:24 | ||||
| chr6:42555927-42556223 | Rare:60 | ||||
| chr6:42704474-42704552 | Rare:28; Clinvar:6; Clinvar (pathogenic):1 | ||||
| chr6:42727017-42727062 | Rare:12 | ||||
| chr6:42742219-42742386 | Common:2; Rare:39 | ||||
| chr6:42742552-42742816 | Common:1; Rare:43 | ||||
| chr6:42745319-42745463 | Rare:40 | ||||
| chr6:42747581-42747673 | Common:1; Rare:21 | ||||
| chr6:42747734-42747841 | Common:3; Rare:35 | ||||
| chr6:42747886-42747987 | Rare:13 | ||||
| chr6:42782665-42783123 | Common:4; Rare:137 | ||||
| chr6:42783169-42783637 | Common:2; Rare:121 | ||||
| chr6:42783641-42783765 | Common:3; Rare:33 |