Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:52340344-52340509 | Common:1; Rare:41 | ||||
chr18:52340575-52340813 | Common:1; Rare:59 | ||||
chr18:54269484-54269622 | Common:1; Rare:69 | ||||
chr18:54357821-54358016 | Common:8; Rare:64 | ||||
chr18:55588108-55588272 | Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
chr18:55589713-55589906 | Rare:54 | ||||
chr18:56651122-56651722 | Common:9; Rare:150 | ||||
chr18:57621713-57621972 | Common:3; Rare:92 | ||||
chr18:58045463-58045761 | Common:4; Rare:76 | ||||
chr18:58045892-58045978 | Rare:14 | ||||
chr18:58046282-58046420 | Common:2; Rare:21 | ||||
chr18:58863346-58863573 | Common:8; Rare:71 | ||||
chr18:58864360-58864502 | Rare:26 | ||||
chr18:58864509-58864918 | Common:1; Rare:84 | ||||
chr18:59139692-59140035 | Common:3; Rare:92 |