| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151452029-151452548 | Common:4; Rare:183 | ||||
| chr6:152302043-152302241 | Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152983037-152983281 | Common:2; Rare:74 | ||||
| chr6:152983476-152983743 | Common:3; Rare:98 | ||||
| chr6:153002513-153003063 | Common:7; Rare:193 | ||||
| chr6:153131219-153131460 | Rare:104 | ||||
| chr6:154733151-154733467 | Common:1; Rare:134 | ||||
| chr6:154734084-154734325 | Common:5; Rare:65 | ||||
| chr6:155314456-155314613 | Common:2; Rare:48 | ||||
| chr6:157323495-157323630 | Common:2; Rare:45 | ||||
| chr6:157715758-157716079 | Rare:47 | ||||
| chr6:158168206-158168388 | Common:2; Rare:63 | ||||
| chr6:158644216-158644374 | Rare:36 | ||||
| chr6:158644704-158644955 | Common:2; Rare:93 | ||||
| chr6:158649834-158650069 | Common:1; Rare:41 |