| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42929209-42929566 | Common:4; Rare:104 | ||||
| chr6:42984284-42984635 | Rare:91 | ||||
| chr6:43013809-43014280 | Common:2; Rare:119 | ||||
| chr6:43040696-43040980 | Rare:74; Clinvar:3 | ||||
| chr6:43053764-43054020 | Common:2; Rare:82; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43076123-43076451 | Rare:102 | ||||
| chr6:43427314-43427580 | Common:1; Rare:54 | ||||
| chr6:43516785-43517112 | Common:6; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576185 | Rare:87; Clinvar:4 | ||||
| chr6:43629158-43629403 | Common:2; Rare:78 | ||||
| chr6:43630027-43630219 | Common:1; Rare:43 | ||||
| chr6:43635564-43635873 | Common:2; Rare:71 | ||||
| chr6:43687768-43687838 | Common:1; Rare:30 | ||||
| chr6:43770070-43770254 | Common:3; Rare:55 | ||||
| chr6:44127342-44127669 | Common:4; Rare:94 |