| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43516745-43517124 | Common:6; Rare:135; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575939-43576224 | Common:1; Rare:116; Clinvar:7 | ||||
| chr6:43629098-43629565 | Common:2; Rare:135 | ||||
| chr6:43687757-43687827 | Common:1; Rare:26 | ||||
| chr6:43770076-43770423 | Common:5; Rare:91 | ||||
| chr6:43770435-43770509 | Rare:14 | ||||
| chr6:43770687-43770802 | Common:1; Rare:36 | ||||
| chr6:43770815-43771310 | Common:1; Rare:158 | ||||
| chr6:43771927-43772022 | Rare:14 | ||||
| chr6:43772796-43772937 | Rare:20 | ||||
| chr6:43773436-43773583 | Common:2; Rare:25 | ||||
| chr6:44126813-44127038 | Common:1; Rare:65 | ||||
| chr6:44127278-44127677 | Common:4; Rare:112 | ||||
| chr6:44219496-44219716 | Common:2; Rare:60 | ||||
| chr6:44223475-44223615 | Common:1; Rare:44 |