| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:49463205-49463413 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr6:52420089-52420378 | Common:3; Rare:124; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995267-52995794 | Common:4; Rare:220 | ||||
| chr6:53348882-53349211 | Common:2; Rare:127 | ||||
| chr6:54846439-54846820 | Common:2; Rare:93 | ||||
| chr6:56542790-56543065 | Common:2; Rare:46 | ||||
| chr6:57172530-57172758 | Common:1; Rare:74 | ||||
| chr6:57221383-57221567 | Rare:41 | ||||
| chr6:57221612-57221643 | Common:1; Rare:11 | ||||
| chr6:57222266-57222439 | Rare:66 | ||||
| chr6:57317507-57317660 | Rare:42 | ||||
| chr6:63572255-63572675 | Rare:150 | ||||
| chr6:63805787-63805797 | Rare:2 | ||||
| chr6:63806332-63806613 | Rare:47; Clinvar:1 | ||||
| chr6:69796883-69797087 | Rare:64; Clinvar:4; Clinvar (benign):1 |