| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:49636829-49637083 | Rare:59 | ||||
| chr6:52420089-52420378 | Common:3; Rare:124; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995267-52995819 | Common:4; Rare:228 | ||||
| chr6:53348876-53349281 | Common:2; Rare:145 | ||||
| chr6:53545098-53545239 | Rare:40 | ||||
| chr6:53665727-53665886 | Common:1; Rare:35 | ||||
| chr6:54846563-54846786 | Common:1; Rare:55 | ||||
| chr6:56542649-56542977 | Common:1; Rare:74 | ||||
| chr6:56543007-56543069 | Rare:8 | ||||
| chr6:57172171-57172326 | Rare:46 | ||||
| chr6:57221383-57221651 | Common:1; Rare:63 | ||||
| chr6:57222247-57222391 | Rare:64 | ||||
| chr6:57317539-57317660 | Rare:36 | ||||
| chr6:63636051-63636149 | Rare:31 | ||||
| chr6:68634956-68635361 | Common:2; Rare:110 |