Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:31651972-31652069 | Rare:25 | ||||
chr6:31652330-31652415 | Common:7; Rare:33 | ||||
chr6:31652593-31652711 | Rare:29 | ||||
chr6:31664911-31665123 | Common:2; Rare:49 | ||||
chr6:31665854-31666149 | Common:3; Rare:82 | ||||
chr6:31703285-31703552 | Common:2; Rare:67 | ||||
chr6:31736356-31736586 | Common:1; Rare:44 | ||||
chr6:31815308-31815546 | Common:1; Rare:71 | ||||
chr6:31897670-31897782 | Rare:21 | ||||
chr6:31958891-31959185 | Rare:91; Clinvar:8 | ||||
chr6:32178091-32178458 | Common:2; Rare:54 | ||||
chr6:32190148-32190475 | Rare:62 | ||||
chr6:32843983-32844108 | Rare:30; Clinvar:1 | ||||
chr6:32844634-32844840 | Common:1; Rare:44 | ||||
chr6:32853690-32853796 | Rare:50; Clinvar:1; Clinvar (benign):1 |