chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG35GENIChomozygous613647600
1228738748228738749AT22GENIChomozygous615907921
1228741236228741248CTCTCTCTCTCT------------4GENIChomozygous736060340
1228741329228741330AAGAGAG27GENIChomozygous736060342
1228741505228741506A-33GENIChomozygous736060343
1228743096228743097AC36GENICheterozygous615907922
1228744220228744221TC18GENIChomozygous615907923
1228744463228744464CA28GENIChomozygous615907924
1228744907228744908CT23GENIChomozygous615907925
1228745221228745222TC27GENIChomozygous615907926
1228745361228745362AG16GENIChomozygous615907927
1228745396228745397TC27GENIChomozygous615907928
1228745721228745722AG41GENIChomozygous615907929
1228746722228746723TC19GENIChomozygous615907930
1228749142228749143GA31GENIChomozygous615907931
1228751658228751659CT34GENIChomozygous615907932
1228751732228751733CCATTT11GENICheterozygous736060344
1228751732228751733CCATTTATTT11GENICpossibly homozygous736060345
1228751914228751915CT40GENIChomozygous615907933
1228752487228752488AG17GENIChomozygous615907934
1228753085228753089ACAC----6GENICheterozygous736060346
1228753087228753089AC--6GENICheterozygous736060347
1228755483228755484AACACAC21GENICpossibly homozygous736060348
1228755486228755487CCACA21GENICpossibly homozygous736060349
1228756439228756440CCT9GENICheterozygous736060351
1228756439228756440CCTT9GENICheterozygous736060352
1228756522228756536GTGTGTGTGTGTGT--------------6GENIChomozygous736060353
1228758692228758693CT26GENIChomozygous615907935
1228758718228758719AG29GENIChomozygous615907936