| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43053797-43054005 | Common:1; Rare:66; Clinvar:5 | ||||
| chr6:43054405-43054594 | Common:1; Rare:69 | ||||
| chr6:43056176-43056374 | Rare:59 | ||||
| chr6:43059812-43060038 | Common:1; Rare:60 | ||||
| chr6:43060192-43060584 | Common:2; Rare:99 | ||||
| chr6:43308761-43308981 | Common:1; Rare:75 | ||||
| chr6:43427500-43427592 | Rare:27 | ||||
| chr6:43516853-43517112 | Common:5; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575943-43576228 | Common:1; Rare:117; Clinvar:8 | ||||
| chr6:43625525-43625779 | Rare:67 | ||||
| chr6:43687757-43687827 | Common:1; Rare:26 | ||||
| chr6:43770076-43770254 | Common:3; Rare:54 | ||||
| chr6:43771670-43772022 | Common:4; Rare:61 | ||||
| chr6:43773456-43773572 | Common:2; Rare:18 | ||||
| chr6:44126519-44126933 | Common:2; Rare:94 |