| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:53065378-53065598 | Common:1; Rare:68 | ||||
| chr6:54846623-54846820 | Common:1; Rare:49 | ||||
| chr6:57172432-57172768 | Common:1; Rare:98 | ||||
| chr6:63572191-63572596 | Rare:147 | ||||
| chr6:63635763-63636149 | Common:1; Rare:126 | ||||
| chr6:68635161-68635331 | Common:1; Rare:51 | ||||
| chr6:70413174-70413602 | Common:2; Rare:130 | ||||
| chr6:73452274-73452583 | Common:2; Rare:55 | ||||
| chr6:73653891-73654174 | Common:3; Rare:76; Clinvar:3 | ||||
| chr6:73696019-73696187 | Common:1; Rare:33 | ||||
| chr6:75284675-75285037 | Common:1; Rare:109 | ||||
| chr6:75601795-75601893 | Rare:42 | ||||
| chr6:75602330-75602527 | Common:1; Rare:57 | ||||
| chr6:75666670-75666741 | Rare:17 | ||||
| chr6:75749120-75749423 | Common:4; Rare:82; Clinvar:3; Clinvar (benign):1 |