| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151325409-151325720 | Common:2; Rare:72 | ||||
| chr6:151391503-151391832 | Common:3; Rare:93 | ||||
| chr6:151452047-151452552 | Common:4; Rare:180 | ||||
| chr6:151807384-151807726 | Common:2; Rare:73 | ||||
| chr6:152983027-152983361 | Common:2; Rare:102 | ||||
| chr6:152983508-152983743 | Common:3; Rare:89 | ||||
| chr6:153002622-153002872 | Common:4; Rare:94 | ||||
| chr6:153131231-153131470 | Rare:106 | ||||
| chr6:157323497-157323639 | Common:2; Rare:44 | ||||
| chr6:158168219-158168378 | Common:2; Rare:55 | ||||
| chr6:158644708-158644972 | Common:2; Rare:92 | ||||
| chr6:158818220-158818366 | Common:3; Rare:58 | ||||
| chr6:158819323-158819450 | Common:2; Rare:47 | ||||
| chr6:158999740-158999886 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:159000141-159000301 | Common:1; Rare:40 |