| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013846-43014280 | Common:2; Rare:104 | ||||
| chr6:43053766-43054121 | Common:2; Rare:98; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059812-43059913 | Rare:34 | ||||
| chr6:43076123-43076563 | Rare:150 | ||||
| chr6:43477319-43477597 | Common:2; Rare:57 | ||||
| chr6:43516822-43517106 | Common:4; Rare:106; Clinvar:2 | ||||
| chr6:43575952-43576234 | Common:1; Rare:117; Clinvar:8 | ||||
| chr6:43629143-43629427 | Common:2; Rare:85 | ||||
| chr6:43687744-43687841 | Common:1; Rare:43 | ||||
| chr6:43770076-43770303 | Common:4; Rare:62 | ||||
| chr6:44127276-44127657 | Common:4; Rare:107 | ||||
| chr6:44246880-44247193 | Common:4; Rare:132 | ||||
| chr6:44387426-44387756 | Common:4; Rare:85 | ||||
| chr6:45377805-45378183 | Common:2; Rare:124 | ||||
| chr6:47477649-47478247 | Common:5; Rare:174; Clinvar:7; Clinvar (benign):7 |