chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95257185452571857CTT---14GENIChomozygous53112522
95257215752572158GA24GENICpossibly homozygous51956689
95257226652572267AG29GENIChomozygous53590244
95257285452572855GT30GENIChomozygous51956695
95257290352572904AG27GENIChomozygous51956698
95257291752572918GT24GENIChomozygous51956701
95257312052573121AG29GENIChomozygous51956704
95257317852573179TC23GENIChomozygous51956707
95257320852573209AT21GENIChomozygous51956710
95257323452573235CA17GENIChomozygous51956713
95257334052573341TA29GENIChomozygous51956716
95257362752573628AG33GENIChomozygous51956719
95257373052573733TAG---34GENIChomozygous51956722
95257378952573790TA26GENIChomozygous51956725
95257419252574193AG30GENIChomozygous51956728
95257448952574490CT26GENIChomozygous51956734
95257469652574697TC21GENIChomozygous51956737
95257473752574738TC33GENIChomozygous51956740
95257512052575121GA27GENIChomozygous51956743
95257545052575451AG18GENIChomozygous51956746
95257567152575672AG5GENIChomozygous51956749
95257593552575936TC13GENIChomozygous53590245
95257628052576281TG29GENIChomozygous51956755
95257632152576322GC27GENIChomozygous51956758
95257661052576611TC23GENIChomozygous51956765
95257665052576651TA22GENIChomozygous51956768
95257683152576832AG31GENIChomozygous51956771
95257701252577013AT34GENIChomozygous51956774
95257741352577414CT36GENIChomozygous51956777
95257750252577503AT29GENIChomozygous51956780
95257784852577849GC17GENIChomozygous53590246