| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:152168217-152168461 | Rare:60 | ||||
| chr6:152302022-152302198 | Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152637227-152637294 | Rare:18 | ||||
| chr6:152983021-152983216 | Common:2; Rare:58 | ||||
| chr6:152983525-152983768 | Common:4; Rare:94 | ||||
| chr6:153002448-153002859 | Common:7; Rare:164 | ||||
| chr6:154510506-154510881 | Common:4; Rare:111 | ||||
| chr6:154733622-154733740 | Common:1; Rare:33 | ||||
| chr6:155314431-155314625 | Common:4; Rare:72 | ||||
| chr6:157323497-157323597 | Common:2; Rare:37 | ||||
| chr6:158168206-158168388 | Common:2; Rare:63 | ||||
| chr6:158644692-158645003 | Common:3; Rare:110 | ||||
| chr6:158818220-158818340 | Common:1; Rare:45 | ||||
| chr6:158999665-158999910 | Common:1; Rare:102; Clinvar:3; Clinvar (benign):4 | ||||
| chr6:159000141-159000305 | Common:1; Rare:41 |