chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396355108396371GTGTGTGTGTGTGTGT----------------5GENICheterozygous51596094
10108396766108396767TC44GENIChomozygous51596096
10108397090108397091GT68GENIChomozygous51596098
10108397871108397872CT40GENIChomozygous51596100
10108397987108397988CT62GENICpossibly homozygous51596102
10108398368108398369AG31GENIChomozygous51596104
10108398863108398864TC48GENIChomozygous51596106
10108399592108399593CT72GENIChomozygous51596108
10108400021108400024TCC---33GENIChomozygous51596110
10108400449108400450AG62GENIChomozygous51596112
10108401441108401449GTGTGTGT--------5GENIChomozygous51596114
10108401486108401487TC30GENICpossibly homozygous51596116
10108402283108402284AG46GENIChomozygous51596118
10108403550108403551TTAAC17GENIChomozygous51596120
10108403553108403554GGGGCTAC7GENIChomozygous51596122
10108403922108403924AA--60GENIChomozygous51596124
10108405663108405664TTC57GENIChomozygous51596126
10108407055108407057TT--21GENIChomozygous51596130
10108401478108401479TC27GENICheterozygous51772050
10108407879108407880AT60GENIChomozygous51596132
10108408887108408888TTC27GENICheterozygous51596134
10108408887108408888TTTC27GENICheterozygous51596136
10108409221108409222TTCA59GENIChomozygous51596138
10108409485108409486AG63GENIChomozygous51596140
10108410258108410259TA47GENICpossibly homozygous51596142
10108410992108410993CT67GENIChomozygous51772052
10108411935108411936CT32GENICheterozygous51596146
10108412065108412066GA51GENIChomozygous51596148
10108412067108412068CCT55GENIChomozygous51596149
10108412225108412226CT57GENIChomozygous51772054
10108412524108412525CT67GENIChomozygous51596151
10108412774108412775TC57GENIChomozygous51596153