chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58854678888546789TG18GENIChomozygous113911589
58854916988549170AG29GENIChomozygous113911592
58854998288549983CT18GENIChomozygous113911594
58855156788551568GA22GENIChomozygous114226904
58855222688552227AC26GENIChomozygous113911598
58855327988553280CT14GENIChomozygous113911600
58855402688554027AG31GENIChomozygous113911605
58855487188554872CT18GENIChomozygous114226905
58855531788555318CG24GENIChomozygous113911607
58855548088555481TC21GENIChomozygous114226906
58855554288555543AG26GENIChomozygous114226907
58855808888558089TC32GENIChomozygous113911613
58855851688558517AC28GENIChomozygous113911615
58855914088559141GC28GENIChomozygous113911619
58855934888559349GA25GENIChomozygous114226909
58856395088563951AT30GENIChomozygous114226910
58856473588564736CT30GENIChomozygous113911626
58856479288564793AC21GENIChomozygous113911628
58856607288566073AG30GENIChomozygous113911634
58856614788566148TA31GENIChomozygous113911636
58856614888566149TA31GENIChomozygous113911637
58856888988568890AG31GENICpossibly homozygous114226911
58857088388570884CT34GENIChomozygous114226912
58857110288571103GA28GENIChomozygous113911644
58857118988571190CT26GENIChomozygous114226913
58857170388571704TC25GENIChomozygous113911646
58857195888571959GC35GENIChomozygous113911648
58857240588572406AT26GENIChomozygous113911650
58857729088577291CT28GENIChomozygous114226914
58858660088586601TC32GENIChomozygous113911670
58859454988594550CA34GENIChomozygous114226915
58861272988612730GC34GENIChomozygous118854456
58861275488612755GA31GENIChomozygous114226917
58861745488617455AG21GENIChomozygous113911734
58862029988620300CT33GENIChomozygous114226918
58862345488623455AG26GENIChomozygous113911764
58862471088624711TG33GENIChomozygous114226919