| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42879583-42879950 | Rare:108 | ||||
| chr6:42890802-42890870 | Rare:31 | ||||
| chr6:42929209-42929578 | Common:4; Rare:111 | ||||
| chr6:42984284-42984630 | Rare:88 | ||||
| chr6:43013869-43014280 | Common:2; Rare:90 | ||||
| chr6:43182143-43182217 | Rare:20 | ||||
| chr6:43427436-43427579 | Rare:38 | ||||
| chr6:43427749-43427902 | Rare:36 | ||||
| chr6:43516835-43517130 | Common:5; Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575921-43576234 | Common:2; Rare:125; Clinvar:8 | ||||
| chr6:43687765-43687994 | Common:2; Rare:69 | ||||
| chr6:43770076-43770230 | Common:2; Rare:47 | ||||
| chr6:43771902-43771990 | Rare:18 | ||||
| chr6:44127342-44127669 | Common:4; Rare:94 | ||||
| chr6:44387439-44387738 | Common:4; Rare:77 |