chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58854678888546789TG25GENIChomozygous113911589
58854916988549170AG29GENIChomozygous113911592
58854998288549983CT20GENIChomozygous113911594
58855156788551568GA17GENIChomozygous114226904
58855222688552227AC19GENIChomozygous113911598
58855327988553280CT39GENIChomozygous113911600
58855402688554027AG23GENIChomozygous113911605
58855487188554872CT28GENIChomozygous114226905
58855531788555318CG32GENIChomozygous113911607
58855548088555481TC31GENIChomozygous114226906
58855554288555543AG30GENIChomozygous114226907
58855808888558089TC29GENIChomozygous113911613
58855851688558517AC35GENIChomozygous113911615
58855914088559141GC26GENIChomozygous113911619
58855934888559349GA22GENIChomozygous114226909
58856395088563951AT37GENIChomozygous114226910
58856473588564736CT29GENIChomozygous113911626
58856479288564793AC32GENIChomozygous113911628
58856607288566073AG21GENIChomozygous113911634
58856614788566148TA27GENIChomozygous113911636
58856614888566149TA26GENIChomozygous113911637
58856888988568890AG47GENIChomozygous114226911
58857045088570451AG41GENIChomozygous113911643
58857088388570884CT28GENICpossibly homozygous114226912
58857110288571103GA27GENIChomozygous113911644
58857118988571190CT29GENIChomozygous114226913
58857170388571704TC22GENIChomozygous113911646
58857195888571959GC24GENIChomozygous113911648
58857240588572406AT31GENIChomozygous113911650
58858660088586601TC26GENIChomozygous113911670
58859454988594550CA28GENIChomozygous114226915
58861272988612730GC35GENIChomozygous118854456
58861275488612755GA35GENIChomozygous114226917
58861745488617455AG30GENIChomozygous113911734
58862029988620300CT40GENIChomozygous114226918
58862345488623455AG24GENIChomozygous113911764
58862471088624711TG25GENIChomozygous114226919