Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161314319-161314425 | Common:2; Rare:49; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749756-161749837 | Rare:35 | ||||
chr1:161766133-161766382 | Common:3; Rare:77 | ||||
chr1:162790533-162790793 | Common:4; Rare:77 | ||||
chr1:163321723-163322077 | Common:1; Rare:93 | ||||
chr1:165768747-165768933 | Common:1; Rare:74 | ||||
chr1:166839322-166839522 | Rare:57 | ||||
chr1:167935950-167936261 | Common:1; Rare:94 | ||||
chr1:167936556-167936941 | Common:1; Rare:138 | ||||
chr1:168178875-168179090 | Common:1; Rare:79 | ||||
chr1:168225712-168226072 | Common:4; Rare:114 | ||||
chr1:169367725-169368271 | Common:3; Rare:116 | ||||
chr1:169485941-169486158 | Rare:52; Clinvar:1 | ||||
chr1:169794890-169795107 | Common:3; Rare:59 | ||||
chr1:170532059-170532182 | Rare:60; Clinvar:1 |