chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG28GENIChomozygous638805370
1228738748228738749AT35GENIChomozygous638805371
1228738907228738908CT16GENIChomozygous638805372
1228741240228741248CTCTCTCT--------4GENICheterozygous750260690
1228741329228741330AAGAGAG18GENIChomozygous750260691
1228741505228741506A-23GENIChomozygous750260692
1228741525228741526A-23GENIChomozygous750260693
1228743096228743097AC27GENICheterozygous638805373
1228744220228744221TC20GENIChomozygous638805374
1228744463228744464CA16GENIChomozygous638805375
1228744907228744908CT25GENIChomozygous638805376
1228745221228745222TC17GENIChomozygous638805377
1228745396228745397TC29GENIChomozygous638805378
1228745721228745722AG29GENIChomozygous638805379
1228746722228746723TC16GENIChomozygous638805380
1228749142228749143GA30GENIChomozygous638805381
1228751658228751659CT19GENIChomozygous638805382
1228751914228751915CT32GENIChomozygous638805383
1228752487228752488AG32GENIChomozygous638805384
1228753035228753036CCCACACACACA7GENICheterozygous750260696
1228753035228753036CCCACACACACACA7GENICheterozygous750260697
1228753087228753089AC--17GENICpossibly homozygous750260699
1228755150228755166CGCGCACACACACACA----------------11GENICheterozygous750260700
1228755467228755468GGCACA29GENICpossibly homozygous750260702
1228756439228756440CCT3GENICheterozygous750260704
1228756439228756440CCTT3GENICheterozygous750260705
1228756522228756536GTGTGTGTGTGTGT--------------4GENIChomozygous750260706
1228758718228758719AG15GENIChomozygous638805385