| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:49463143-49463407 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52576944-52577248 | Common:6; Rare:100 | ||||
| chr6:52671066-52671167 | Rare:28 | ||||
| chr6:52995259-52995817 | Common:4; Rare:229 | ||||
| chr6:53065379-53065470 | Common:1; Rare:29 | ||||
| chr6:53065566-53065695 | Rare:30 | ||||
| chr6:53348847-53349227 | Common:2; Rare:157 | ||||
| chr6:56541967-56542241 | Rare:41 | ||||
| chr6:56542689-56543086 | Common:2; Rare:80 | ||||
| chr6:56843056-56843494 | Common:1; Rare:116 | ||||
| chr6:57172451-57172810 | Common:1; Rare:103 | ||||
| chr6:57221605-57221685 | Common:1; Rare:21 | ||||
| chr6:57221724-57221803 | Rare:19 | ||||
| chr6:57221959-57222400 | Rare:146 | ||||
| chr6:63636040-63636149 | Rare:35 |