chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT23GENIChomozygous993816061
5159590355159590356AC30GENIChomozygous993816062
5159590356159590357GC30GENIChomozygous993816063
5159590377159590378GA28GENICpossibly homozygous993816064
5159590516159590517AG22GENIChomozygous993816065
5159590543159590544TC21GENIChomozygous993816066
5159590567159590568TC20GENIChomozygous993816067
5159590810159590811GA23GENIChomozygous993816068
5159591041159591042CT15GENIChomozygous993816069
5159591165159591166AG35GENIChomozygous993816070
5159591294159591295GA38GENIChomozygous993816071
5159591492159591493CT33GENIChomozygous993816072
5159591711159591712GA30GENIChomozygous993816073
5159592241159592242AG28GENIChomozygous993816074
5159592551159592552GA31GENIChomozygous993816075
5159592593159592594GA40GENIChomozygous993816076
5159592713159592714CT23GENIChomozygous993816077
5159593011159593012TA21GENIChomozygous993816078
5159593229159593230AG27GENIChomozygous993816079
5159593231159593232AC28GENICheterozygous993816080
5159593316159593317AC37GENIChomozygous993816081
5159594481159594482GA23GENICpossibly homozygous993816082
5159595521159595522GA36GENIChomozygous993816083
5159598268159598269GA33GENICpossibly homozygous993816084
5159599504159599505TC12GENIChomozygous993816085
5159599700159599701CT27GENICheterozygous993816086
5159600471159600472TC20GENIChomozygous993816087
5159601143159601144CT29GENIChomozygous993816088
5159601217159601218AG23GENIChomozygous993816089
5159601274159601275AG38GENIChomozygous993816090
5159602018159602019CT9GENIChomozygous993816091