Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:193059264-193059422 | Rare:68 | ||||
chr1:193059447-193059733 | Rare:147 | ||||
chr1:193105373-193105533 | Common:3; Rare:68 | ||||
chr1:193121721-193122210 | Common:3; Rare:177; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:193122441-193122471 | Rare:10 | ||||
chr1:193186605-193186811 | Rare:38 | ||||
chr1:197902529-197902652 | Common:1; Rare:41 | ||||
chr1:200042292-200042613 | Common:1; Rare:71 | ||||
chr1:200042656-200042875 | Common:1; Rare:50 | ||||
chr1:200669842-200670041 | Common:12; Rare:78 | ||||
chr1:201469131-201469525 | Common:4; Rare:123 | ||||
chr1:201786302-201786509 | Common:1; Rare:43 | ||||
chr1:201828972-201829212 | Rare:94 | ||||
chr1:201888413-201888682 | Common:2; Rare:60 | ||||
chr1:201946284-201946296 | Rare:2 |