chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG51GENIChomozygous502581782
1228738748228738749AT36GENIChomozygous505782977
1228741237228741238TG29GENICpossibly homozygous505782978
1228741239228741240TG28GENICheterozygous505782979
1228741329228741330AAGAGAG17GENIChomozygous683441452
1228741505228741506A-20GENIChomozygous683441453
1228741525228741526A-17GENIChomozygous683441454
1228743096228743097AC41GENICheterozygous505782980
1228743588228743589TG50GENICheterozygous505782981
1228744220228744221TC56GENIChomozygous505782982
1228744463228744464CA42GENIChomozygous505782983
1228744907228744908CT47GENIChomozygous505782984
1228745221228745222TC65GENIChomozygous505782985
1228745396228745397TC26GENIChomozygous505782986
1228745721228745722AG52GENIChomozygous505782987
1228746722228746723TC43GENIChomozygous505782988
1228749142228749143GA49GENIChomozygous505782989
1228750707228750708G-2GENIChomozygous683441455
1228751658228751659CT23GENIChomozygous505782990
1228751732228751733CCATTT1GENIChomozygous683441456
1228751914228751915CT56GENIChomozygous505782991
1228752487228752488AG49GENIChomozygous505782992
1228753035228753036CCCACA6GENIChomozygous683441457
1228753085228753089ACAC----16GENICheterozygous683441458
1228753087228753089AC--16GENICheterozygous683441459
1228754285228754286CCT15GENICheterozygous683441460
1228755467228755468GGCA33GENIChomozygous683441461
1228755483228755484AACACAC38GENICheterozygous683441462
1228755483228755484AACACACAC38GENICheterozygous683441463
1228755484228755485TC46GENICheterozygous505782993
1228755486228755487CCACA34GENICheterozygous683441465
1228755487228755488T-34GENICheterozygous683441464
1228755487228755488TTACAC33GENIChomozygous683441467
1228755506228755507TA44GENICheterozygous505782994
1228756439228756440CCT5GENICheterozygous683441468
1228756440228756441T-5GENICheterozygous683441469
1228756522228756528GTGTGT------6GENIChomozygous683441471
1228758692228758693CT56GENIChomozygous505782995
1228758718228758719AG51GENIChomozygous505782996