| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42929394-42929562 | Common:1; Rare:58 | ||||
| chr6:42979173-42979334 | Common:3; Rare:49; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:42984322-42984629 | Rare:75 | ||||
| chr6:43013869-43014304 | Common:2; Rare:98 | ||||
| chr6:43182084-43182223 | Rare:40 | ||||
| chr6:43427431-43427576 | Rare:38 | ||||
| chr6:43427734-43427893 | Rare:33 | ||||
| chr6:43477483-43477589 | Rare:21 | ||||
| chr6:43516850-43517124 | Common:5; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576190 | Rare:90; Clinvar:4 | ||||
| chr6:43635793-43635893 | Common:1; Rare:28 | ||||
| chr6:43687768-43687838 | Common:1; Rare:30 | ||||
| chr6:43770070-43770230 | Common:2; Rare:48 | ||||
| chr6:43771906-43771986 | Rare:17 | ||||
| chr6:44127346-44127657 | Common:4; Rare:92 |