Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:150778625-150778817 | Common:3; Rare:77 | ||||
chr5:151540732-151540972 | Common:1; Rare:50 | ||||
chr5:180830724-180831019 | Common:1; Rare:89 | ||||
chr5:180831582-180831669 | Common:2; Rare:38 | ||||
chr6:1111200-1111461 | Common:2; Rare:61 | ||||
chr6:4018688-4018831 | Common:2; Rare:45 | ||||
chr6:13813808-13813847 | Rare:11 | ||||
chr6:19839029-19839135 | Rare:40 | ||||
chr6:29888079-29888194 | Common:12; Rare:80 | ||||
chr6:29944276-29944550 | Common:21; Rare:67 | ||||
chr6:31121448-31121589 | Common:1; Rare:26 | ||||
chr6:31400599-31400721 | Common:4; Rare:27 | ||||
chr6:31720120-31720497 | Common:2; Rare:72 | ||||
chr6:32853037-32853197 | Rare:41; Clinvar (benign):2 | ||||
chr6:32894586-32894807 | Common:6; Rare:61 |