| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43427716-43427925 | Rare:57 | ||||
| chr6:43477461-43477597 | Rare:29 | ||||
| chr6:43516850-43517123 | Common:5; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575909-43576234 | Common:2; Rare:129; Clinvar:8 | ||||
| chr6:43627287-43627492 | Rare:30 | ||||
| chr6:43628806-43628920 | Rare:38 | ||||
| chr6:43629130-43629503 | Common:2; Rare:105 | ||||
| chr6:43630029-43630133 | Common:1; Rare:23 | ||||
| chr6:43635622-43635893 | Common:2; Rare:63 | ||||
| chr6:43687731-43687848 | Common:1; Rare:52 | ||||
| chr6:43770081-43770231 | Common:2; Rare:46 | ||||
| chr6:43770626-43770808 | Common:1; Rare:55 | ||||
| chr6:43771906-43772022 | Rare:21 | ||||
| chr6:44127346-44127665 | Common:4; Rare:93 | ||||
| chr6:44223480-44223821 | Common:2; Rare:105 |