| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151325447-151325749 | Common:2; Rare:71 | ||||
| chr6:151452053-151452548 | Common:4; Rare:177 | ||||
| chr6:152302071-152302161 | Rare:29; Clinvar (benign):1 | ||||
| chr6:152983525-152983754 | Common:4; Rare:88 | ||||
| chr6:153002643-153002838 | Common:3; Rare:70 | ||||
| chr6:154510522-154510776 | Common:2; Rare:78 | ||||
| chr6:155314456-155314618 | Common:2; Rare:50 | ||||
| chr6:157323497-157323642 | Common:2; Rare:45 | ||||
| chr6:158168219-158168382 | Common:2; Rare:57 | ||||
| chr6:158644704-158644871 | Common:2; Rare:74 | ||||
| chr6:158649872-158650060 | Rare:37 | ||||
| chr6:158818106-158818266 | Common:2; Rare:61 | ||||
| chr6:158819316-158819450 | Common:2; Rare:50 | ||||
| chr6:158999746-158999910 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:159000193-159000268 | Rare:18 |