chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2075213907521391T17GENIChomozygous129655786
2075213917521392AG17GENIChomozygous109542469
2075213957521395G17GENIChomozygous129655787
2075213967521397CG17GENIChomozygous109542471
2075213997521400TC18GENIChomozygous109542473
2075214017521402AG18GENIChomozygous109542475
2075214077521408AG17GENIChomozygous124631706
2075214237521432AAAACCCTT15GENIChomozygous129655788
2075214357521439TCTA14GENIChomozygous129655789
2075214597521459T14GENIChomozygous129655790
2075214617521462AG14GENIChomozygous129708244
2075214667521467AG14GENIChomozygous129708245
2075214727521473AG14GENIChomozygous129708246
2075214727521472GTGG14GENIChomozygous129655791
2075214757521475GC14GENIChomozygous129655792
2075214767521477TG13GENIChomozygous129708247
2075214787521478GGG13GENIChomozygous129655793
2075214807521480ACCCACT12GENIChomozygous129655794
2075214817521482AC12GENIChomozygous129708248
2075214857521485TTC10GENIChomozygous129655795
2075214887521489AT11GENIChomozygous129708249
2075214907521490GTCTTT11GENIChomozygous129655796
2075214917521492TC12GENIChomozygous129708250
2075214987521498TTTC12GENIChomozygous129655797
2075215367521537T14GENIChomozygous129655798
2075215417521542A14GENIChomozygous129655799
2075214457521456CAACAACAAAA14GENIChomozygous130490077
2075744757574505CTCATAATGTCATAACCGTGGTGTGTGTGT6GENIChomozygous130490078
2075846647584666CT22GENICheterozygous129655813
2075733287573329CT16GENIChomozygous133517669