Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:15684287-15684348 | Common:1; Rare:19 | ||||
chr17:15699509-15699799 | Common:3; Rare:77 | ||||
chr17:15999590-15999992 | Common:3; Rare:179; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr17:17237113-17237420 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):3 | ||||
chr17:17591589-17591956 | Common:2; Rare:106 | ||||
chr17:18087854-18087997 | Rare:44 | ||||
chr17:18183649-18183925 | Rare:119 | ||||
chr17:18247670-18247983 | Common:1; Rare:129 | ||||
chr17:18254649-18254824 | Rare:56 | ||||
chr17:18314895-18315326 | Common:1; Rare:119 | ||||
chr17:18682211-18682342 | Common:4; Rare:16 | ||||
chr17:18697973-18698013 | Common:1; Rare:8 | ||||
chr17:18856195-18856372 | Common:1; Rare:30 | ||||
chr17:19377622-19377781 | Common:2; Rare:39 | ||||
chr17:19377902-19378028 | Common:1; Rare:30 |