| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43516785-43517141 | Common:6; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575939-43576234 | Common:1; Rare:120; Clinvar:8 | ||||
| chr6:43628836-43628904 | Rare:22 | ||||
| chr6:43629143-43629484 | Common:2; Rare:96 | ||||
| chr6:43630029-43630196 | Common:1; Rare:36 | ||||
| chr6:43687757-43688050 | Common:2; Rare:85 | ||||
| chr6:43770050-43770332 | Common:6; Rare:80 | ||||
| chr6:43770614-43770797 | Common:1; Rare:50 | ||||
| chr6:43771192-43771266 | Common:1; Rare:32 | ||||
| chr6:43771941-43772022 | Rare:10 | ||||
| chr6:43772806-43772988 | Common:1; Rare:25 | ||||
| chr6:44127272-44127677 | Common:4; Rare:114 | ||||
| chr6:44246904-44247192 | Common:4; Rare:120 | ||||
| chr6:44247832-44248000 | Common:1; Rare:54 | ||||
| chr6:44257480-44257770 | Rare:76 |