Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169367728-169368306 | Common:4; Rare:122 | ||||
chr1:169485901-169486148 | Rare:63; Clinvar:2 | ||||
chr1:169794875-169795058 | Common:3; Rare:38 | ||||
chr1:170531939-170532169 | Common:2; Rare:69 | ||||
chr1:171485362-171485593 | Rare:86 | ||||
chr1:171841354-171841543 | Common:3; Rare:58 | ||||
chr1:173477148-173477492 | Common:4; Rare:126 | ||||
chr1:173714863-173714937 | Rare:14 | ||||
chr1:173824397-173824738 | Rare:61; Clinvar:2 | ||||
chr1:173824870-173824886 | Rare:4 | ||||
chr1:174159268-174159545 | Common:4; Rare:96 | ||||
chr1:179081889-179082102 | Common:1; Rare:65 | ||||
chr1:179882474-179882707 | Rare:111; Clinvar:2; Clinvar (benign):2 | ||||
chr1:179882725-179882861 | Rare:62; Clinvar:5 | ||||
chr1:182391327-182391520 | Common:1; Rare:45 |