Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:30006273-30006731 | Common:7; Rare:67 | ||||
chr6:30288735-30288873 | Common:4; Rare:24 | ||||
chr6:30491134-30491670 | Common:2; Rare:139 | ||||
chr6:30723179-30723398 | Rare:37 | ||||
chr6:31400594-31400740 | Common:5; Rare:29 | ||||
chr6:31734752-31734907 | Rare:28 | ||||
chr6:31822070-31822270 | Common:2; Rare:39 | ||||
chr6:32442203-32442557 | Common:7; Rare:72 | ||||
chr6:32894079-32894298 | Common:3; Rare:40 | ||||
chr6:32894543-32894874 | Common:13; Rare:97 | ||||
chr6:33249404-33249612 | Rare:68 | ||||
chr6:33425670-33425872 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
chr6:33593160-33593389 | Common:2; Rare:80 | ||||
chr6:33623108-33623195 | Rare:19 | ||||
chr6:33633600-33633879 | Common:5; Rare:81 |