| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151452029-151452538 | Common:4; Rare:177 | ||||
| chr6:152983009-152983351 | Common:2; Rare:105 | ||||
| chr6:153131207-153131491 | Rare:123 | ||||
| chr6:155314456-155314764 | Common:9; Rare:109 | ||||
| chr6:157323497-157323598 | Common:2; Rare:37 | ||||
| chr6:158168200-158168402 | Common:2; Rare:73; Clinvar:1 | ||||
| chr6:158818216-158818373 | Common:3; Rare:61 | ||||
| chr6:159000141-159000292 | Common:1; Rare:38 | ||||
| chr6:159693219-159693594 | Common:6; Rare:105 | ||||
| chr6:159726918-159727162 | Common:1; Rare:94 | ||||
| chr6:159727347-159727673 | Common:5; Rare:135 | ||||
| chr6:159789538-159790025 | Common:5; Rare:160 | ||||
| chr6:166342513-166342617 | Common:2; Rare:40 | ||||
| chr6:166999074-166999410 | Common:1; Rare:114 | ||||
| chr6:169751521-169751644 | Rare:44; Clinvar (benign):1 |