chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG29GENIChomozygous635387629
1228739709228739710AG29GENIChomozygous635387630
1228739864228739868CCCC----14GENIChomozygous748070422
1228741329228741330AAGAGAG21GENIChomozygous748070423
1228741505228741506A-13GENIChomozygous748070424
1228741525228741526A-11GENIChomozygous748070425
1228741819228741820CCG20GENIChomozygous748070426
1228743086228743096AAAAAAAAAA----------29GENICheterozygous748070427
1228744220228744221TC30GENIChomozygous635387631
1228745418228745419CT32GENIChomozygous635387632
1228746722228746723TC26GENIChomozygous635387633
1228747028228747043CTGGCATTGTGGTAG---------------28GENIChomozygous748070428
1228751732228751733CCATTT10GENIChomozygous748070429
1228752487228752488AG37GENIChomozygous635387634
1228752836228752837G-27GENIChomozygous748070431
1228753035228753036CCCACA8GENIChomozygous748070433
1228753085228753089ACAC----16GENIChomozygous748070436
1228754008228754009T-25GENIChomozygous748070438
1228755143228755145GC--8GENIChomozygous748070439
1228755467228755468GGCA39GENICpossibly homozygous748070440
1228756439228756440CCT10GENICheterozygous748070443
1228756439228756440CCTT10GENICheterozygous748070444
1228756440228756441T-10GENICheterozygous748070442
1228756521228756522AAGT8GENICpossibly homozygous748070448