| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32894625-32894827 | Common:4; Rare:114 | ||||
| chr6:33249191-33249614 | Common:3; Rare:241 | ||||
| chr6:33425530-33425863 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr6:34657320-34657782 | Common:4; Rare:122 | ||||
| chr6:35318210-35318680 | Common:5; Rare:161 | ||||
| chr6:35566251-35566958 | Common:15; Rare:124 | ||||
| chr6:36667060-36667420 | Common:2; Rare:111 | ||||
| chr6:36677700-36678130 | Common:2; Rare:80 | ||||
| chr6:36819840-36820190 | Common:2; Rare:57 | ||||
| chr6:36829910-36830220 | Common:2; Rare:45 | ||||
| chr6:37059260-37059690 | Common:4; Rare:137 | ||||
| chr6:37083422-37083904 | Common:9; Rare:198 | ||||
| chr6:37102250-37102970 | Common:3; Rare:159 | ||||
| chr6:37104510-37104982 | Common:6; Rare:130 | ||||
| chr6:37105170-37105690 | Common:6; Rare:204 |