chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG29GENIChomozygous529395365
1228738748228738749AT34GENIChomozygous532297847
1228738907228738908CT20GENIChomozygous532297848
1228741239228741240TG9GENICpossibly homozygous532297849
1228741329228741330AAGAGAG11GENIChomozygous693508318
1228741505228741506A-14GENIChomozygous693508319
1228741525228741526A-13GENIChomozygous693508320
1228743096228743097AC24GENICheterozygous532297850
1228744220228744221TC24GENIChomozygous532297851
1228744463228744464CA17GENIChomozygous532297852
1228744907228744908CT26GENICpossibly homozygous532297853
1228745221228745222TC17GENIChomozygous532297854
1228745396228745397TC30GENIChomozygous532297855
1228745721228745722AG29GENIChomozygous532297856
1228746722228746723TC18GENICpossibly homozygous532297857
1228749142228749143GA30GENIChomozygous532297858
1228750707228750708G-1GENIChomozygous693508321
1228751658228751659CT19GENIChomozygous532297859
1228751914228751915CT38GENICpossibly homozygous532297860
1228752487228752488AG32GENIChomozygous532297861
1228753035228753036CCCACA9GENIChomozygous693508322
1228753087228753089AC--9GENICheterozygous693508324
1228754285228754286CCT9GENICpossibly homozygous693508325
1228754312228754313AT16GENICheterozygous532297862
1228755467228755468GGCA14GENIChomozygous693508326
1228755483228755484AACACAC13GENICheterozygous693508327
1228755483228755484AACACACAC13GENICheterozygous693508328
1228755486228755487CCACA11GENICheterozygous693508330
1228755487228755488T-11GENICheterozygous693508329
1228755487228755488TTACAC12GENIChomozygous693508332
1228755506228755507TA21GENICheterozygous532297863
1228756439228756440CCT1GENIChomozygous693508333
1228756522228756528GTGTGT------2GENIChomozygous693508336
1228758718228758719AG18GENIChomozygous532297864