| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43427333-43427572 | Common:1; Rare:48 | ||||
| chr6:43427663-43427925 | Rare:65 | ||||
| chr6:43516887-43517130 | Common:4; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575957-43576196 | Rare:95; Clinvar:4 | ||||
| chr6:43629115-43629514 | Common:2; Rare:114 | ||||
| chr6:43770081-43770531 | Common:5; Rare:108 | ||||
| chr6:43770614-43770899 | Common:1; Rare:85 | ||||
| chr6:44127369-44127639 | Common:4; Rare:75 | ||||
| chr6:44219494-44219737 | Common:2; Rare:64 | ||||
| chr6:44223441-44223615 | Common:1; Rare:51 | ||||
| chr6:44246880-44247193 | Common:4; Rare:132 | ||||
| chr6:44247738-44247768 | Rare:8 | ||||
| chr6:44387445-44387810 | Common:4; Rare:100 | ||||
| chr6:45377649-45377693 | Common:1; Rare:14 | ||||
| chr6:45377807-45378122 | Common:2; Rare:102 |