chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4176994748176994749CT23GENIChomozygous119320525
4176994921176994922TA40GENIChomozygous113407099
4176995409176995410CA29GENIChomozygous113407102
4176995909176995910GA23GENIChomozygous113407104
4176995940176995941CT26GENIChomozygous113407106
4176996202176996203CG21GENIChomozygous113407108
4176996370176996371CT18GENIChomozygous113407110
4176996668176996669TC27GENIChomozygous112966595
4176996669176996670GA28GENIChomozygous113407112
4176996718176996719AG26GENIChomozygous112966597
4176997600176997601GA26GENIChomozygous113407114
4176999157176999158AG23GENIChomozygous112966601
4177000221177000222GA28GENIChomozygous113407116
4177001590177001591TC25GENIChomozygous112966605
4177002789177002790TC29GENIChomozygous112966609
4177003625177003626CA19GENIChomozygous113407122
4177003940177003941GA14GENIChomozygous112966622
4177004005177004006GA22GENIChomozygous113407124
4177004172177004173AG29GENIChomozygous113407126
4177004242177004243CT22GENIChomozygous113407128
4177004384177004385GA16GENIChomozygous112966624
4177004591177004592AG12GENIChomozygous113407132
4177004914177004915CT16GENIChomozygous112966628
4177005146177005147TC18GENIChomozygous112966630
4177005341177005342GA31GENIChomozygous113407134
4177005712177005713AC25GENIChomozygous112966632
4177005978177005979AG22GENIChomozygous112966634
4177008847177008848CT21GENIChomozygous113407138
4177009047177009048TC21GENIChomozygous112966640
4177009118177009119GC26GENIChomozygous113407140
4177009425177009426AT25GENIChomozygous112966642
4177009844177009845GA33GENIChomozygous113407142