chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396355108396371GTGTGTGTGTGTGTGT----------------5GENIChomozygous51596094
10108396766108396767TC42GENIChomozygous51596096
10108397090108397091GT31GENIChomozygous51596098
10108397871108397872CT38GENIChomozygous51596100
10108397987108397988CT50GENIChomozygous51596102
10108398368108398369AG32GENIChomozygous51596104
10108398863108398864TC27GENIChomozygous51596106
10108399592108399593CT31GENIChomozygous51596108
10108400021108400024TCC---38GENIChomozygous51596110
10108400449108400450AG37GENIChomozygous51596112
10108401441108401449GTGTGTGT--------6GENICheterozygous51596114
10108401486108401487TC15GENICheterozygous51596116
10108402283108402284AG32GENIChomozygous51596118
10108403550108403551TTAAC18GENIChomozygous51596120
10108403553108403554GGGGCTAC8GENIChomozygous51596122
10108403922108403924AA--31GENIChomozygous51596124
10108405663108405664TTC25GENIChomozygous51596126
10108406935108406936AAGT7GENICheterozygous51596128
10108407055108407057TT--10GENIChomozygous51596130
10108401478108401479TC18GENICheterozygous51772050
10108407879108407880AT47GENIChomozygous51596132
10108408887108408888TTC17GENICheterozygous51596134
10108408887108408888TTTC17GENICheterozygous51596136
10108409221108409222TTCA7GENICheterozygous51596138
10108409485108409486AG28GENIChomozygous51596140
10108410258108410259TA38GENIChomozygous51596142
10108411238108411239GA36GENIChomozygous51596144
10108411935108411936CT22GENICheterozygous51596146
10108412065108412066GA33GENIChomozygous51596148
10108412067108412068CCT36GENIChomozygous51596149
10108412524108412525CT29GENIChomozygous51596151
10108412774108412775TC41GENIChomozygous51596153