| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42956710-42956766 | Common:2; Rare:9 | ||||
| chr6:44249412-44249888 | Common:1; Rare:136 | ||||
| chr6:44251730-44252264 | Common:3; Rare:180 | ||||
| chr6:44253041-44253603 | Common:6; Rare:188 | ||||
| chr6:50843003-50843150 | Rare:44; Clinvar (benign):1 | ||||
| chr6:53793605-53793809 | Common:2; Rare:31 | ||||
| chr6:53933413-53933625 | Rare:45 | ||||
| chr6:57961351-57961653 | Common:2; Rare:93 | ||||
| chr6:71289945-71289968 | Rare:3 | ||||
| chr6:71296502-71296815 | Common:1; Rare:68 | ||||
| chr6:73517827-73518272 | Common:2; Rare:119 | ||||
| chr6:78985427-78985474 | Rare:17 | ||||
| chr6:85678668-85678910 | Rare:96 | ||||
| chr6:89720870-89721161 | Common:3; Rare:46 | ||||
| chr6:106563524-106563824 | Common:1; Rare:53 |