| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013869-43014339 | Common:2; Rare:101 | ||||
| chr6:43053778-43053958 | Common:2; Rare:67; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059811-43060031 | Common:1; Rare:58 | ||||
| chr6:43060358-43060585 | Rare:43 | ||||
| chr6:43308796-43308992 | Common:1; Rare:57 | ||||
| chr6:43516730-43517124 | Common:6; Rare:141; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576233 | Common:1; Rare:112; Clinvar:8 | ||||
| chr6:43626260-43626564 | Rare:56 | ||||
| chr6:43628832-43628927 | Rare:34 | ||||
| chr6:43629162-43629469 | Common:2; Rare:88 | ||||
| chr6:43687744-43687827 | Common:1; Rare:34 | ||||
| chr6:43770087-43770316 | Common:4; Rare:63 | ||||
| chr6:43771670-43772022 | Common:4; Rare:61 | ||||
| chr6:44126481-44126919 | Common:2; Rare:94 | ||||
| chr6:44127272-44127677 | Common:4; Rare:114 |