| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149749523-149749785 | Rare:115 | ||||
| chr6:149941869-149942030 | Common:4; Rare:28 | ||||
| chr6:151452032-151452548 | Common:4; Rare:182 | ||||
| chr6:152983005-152983353 | Common:2; Rare:107 | ||||
| chr6:152983499-152983720 | Common:3; Rare:81 | ||||
| chr6:153002643-153002798 | Common:2; Rare:59 | ||||
| chr6:153131219-153131498 | Rare:126 | ||||
| chr6:154995216-154995311 | Rare:27 | ||||
| chr6:157323503-157323593 | Common:2; Rare:32 | ||||
| chr6:158168219-158168388 | Common:2; Rare:61 | ||||
| chr6:158644710-158644930 | Common:2; Rare:83 | ||||
| chr6:158818229-158818358 | Common:3; Rare:51 | ||||
| chr6:158819325-158819457 | Common:2; Rare:49 | ||||
| chr6:158999767-158999886 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159693297-159693597 | Common:4; Rare:80 |