| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42984280-42984625 | Rare:86 | ||||
| chr6:43013869-43014334 | Common:2; Rare:101 | ||||
| chr6:43059820-43059890 | Rare:23 | ||||
| chr6:43182105-43182233 | Rare:37 | ||||
| chr6:43186731-43187046 | Rare:79 | ||||
| chr6:43226362-43226483 | Common:1; Rare:24 | ||||
| chr6:43427369-43427602 | Rare:56 | ||||
| chr6:43516791-43517141 | Common:6; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575911-43576186 | Common:1; Rare:103; Clinvar:4 | ||||
| chr6:43629165-43629578 | Common:2; Rare:115 | ||||
| chr6:43687750-43688077 | Common:2; Rare:94 | ||||
| chr6:43770087-43770235 | Common:2; Rare:45 | ||||
| chr6:43771912-43772006 | Rare:17 | ||||
| chr6:44127369-44127676 | Common:4; Rare:90 | ||||
| chr6:44134918-44135045 | Rare:22 |