Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61724952-61725220 | Rare:115 | ||||
chr1:61742347-61742553 | Rare:60 | ||||
chr1:62436255-62436419 | Common:2; Rare:49 | ||||
chr1:62436729-62437193 | Common:1; Rare:126 | ||||
chr1:62688260-62688553 | Common:1; Rare:112; Clinvar:1 | ||||
chr1:62688600-62688627 | Rare:8 | ||||
chr1:62784047-62784180 | Rare:50 | ||||
chr1:63367517-63367691 | Rare:53; Clinvar (benign):1 | ||||
chr1:63523152-63523602 | Common:3; Rare:123 | ||||
chr1:63593330-63593472 | Rare:58; Clinvar (benign):1 | ||||
chr1:63593503-63593699 | Rare:97; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:63773767-63774074 | Rare:65 | ||||
chr1:64203413-64203695 | Rare:67 | ||||
chr1:64204029-64204114 | Rare:31 | ||||
chr1:64841297-64841589 | Rare:71; Clinvar:2 |