| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43041019-43041247 | Common:1; Rare:53; Clinvar (benign):1 | ||||
| chr6:43059833-43059890 | Rare:21 | ||||
| chr6:43427366-43427578 | Rare:51 | ||||
| chr6:43427783-43427893 | Rare:23 | ||||
| chr6:43516887-43517151 | Common:4; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575957-43576199 | Rare:95; Clinvar:4 | ||||
| chr6:43635807-43635893 | Common:1; Rare:25 | ||||
| chr6:43687768-43687841 | Common:1; Rare:31 | ||||
| chr6:43770070-43770222 | Common:2; Rare:45 | ||||
| chr6:43771934-43771985 | Rare:8 | ||||
| chr6:44127358-44127665 | Common:4; Rare:88 | ||||
| chr6:44219496-44219765 | Common:2; Rare:74 | ||||
| chr6:44223453-44223821 | Common:2; Rare:110 | ||||
| chr6:44246854-44247178 | Common:5; Rare:137 | ||||
| chr6:44387445-44387761 | Common:4; Rare:85 |