chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148635856886358569AG21GENICheterozygous118704063
148635857786358578AG17GENICheterozygous118704064
148635857886358579AG18GENICheterozygous118704065
148635859186358592AG22GENICheterozygous118704066
148636047786360478TC39GENIChomozygous113501868
148636176186361762AT31GENICpossibly homozygous114166429
148636188386361884CT39GENICheterozygous118704067
148636200686362007TC39GENICpossibly homozygous113912081
148636669986366700GA80GENICheterozygous118704068
148638058486380585AG4GENIChomozygous118704069
148639481486394815TC52GENIChomozygous113501870
148641652086416521GT19GENIChomozygous113501874
148641656686416567GT17GENIChomozygous118704070
148641669586416696GT6GENIChomozygous118704071
148641669986416700AT6GENIChomozygous118704072
148641675486416755GT19GENIChomozygous118704073
148641675586416756GT19GENIChomozygous118704074
148642384686423847GA70GENICheterozygous118704075
148642388486423885TC55GENICheterozygous118704076
148642388686423887GA54GENICheterozygous118704077
148644485786444858TA27GENIChomozygous113501876
148644487986444880CT21GENIChomozygous113501878
148644488186444882AT21GENIChomozygous113501880
148644488386444884GT22GENIChomozygous113501882
148644488886444889AT22GENIChomozygous113501884
148645161786451618CA35GENICpossibly homozygous118704078
148646157186461572GC63GENICheterozygous118704079
148646163386461634GC102GENICheterozygous118704080
148646167386461674TA103GENICheterozygous118704081
148646168086461681AC97GENICheterozygous118704082
148646169686461697CA78GENICheterozygous118704083
148646170186461702TA66GENICheterozygous118704084
148646267886462679AT83GENICheterozygous118704085
148646326086463261GA107GENICheterozygous118704086
148646403286464033CA200GENICheterozygous118704087
148646413186464132CT235GENICheterozygous118704088
148655316986553170CT9GENIChomozygous118704089
148655327986553280CG22GENIChomozygous118704090