| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158168219-158168388 | Common:2; Rare:61 | ||||
| chr6:158644704-158644933 | Common:2; Rare:89 | ||||
| chr6:158649839-158650069 | Common:1; Rare:41 | ||||
| chr6:158818203-158818538 | Common:7; Rare:115 | ||||
| chr6:158819316-158819446 | Common:2; Rare:49 | ||||
| chr6:158999767-158999941 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:159000130-159000282 | Common:1; Rare:40 | ||||
| chr6:159693148-159693594 | Common:6; Rare:132 | ||||
| chr6:159726911-159727175 | Common:1; Rare:103 | ||||
| chr6:159727323-159727682 | Common:5; Rare:145 | ||||
| chr6:159761828-159762077 | Common:4; Rare:123 | ||||
| chr6:159762309-159762524 | Common:2; Rare:62 | ||||
| chr6:159789534-159789990 | Common:4; Rare:153 | ||||
| chr6:160991686-160991801 | Common:1; Rare:41 | ||||
| chr6:162727713-162727974 | Rare:88; Clinvar:1 |