chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396355108396371GTGTGTGTGTGTGTGT----------------3GENIChomozygous51596094
10108396766108396767TC43GENIChomozygous51596096
10108397090108397091GT43GENIChomozygous51596098
10108397871108397872CT39GENIChomozygous51596100
10108397987108397988CT48GENIChomozygous51596102
10108398368108398369AG29GENIChomozygous51596104
10108398863108398864TC33GENIChomozygous51596106
10108399592108399593CT49GENIChomozygous51596108
10108400021108400024TCC---18GENIChomozygous51596110
10108400449108400450AG30GENIChomozygous51596112
10108401486108401487TC14GENICpossibly homozygous51596116
10108402283108402284AG45GENIChomozygous51596118
10108403550108403551TTAAC10GENIChomozygous51596120
10108403553108403554GGGGCTAC6GENIChomozygous51596122
10108403922108403924AA--34GENIChomozygous51596124
10108405663108405664TTC33GENIChomozygous51596126
10108406935108406936AAGT3GENIChomozygous51596128
10108407055108407057TT--16GENIChomozygous51596130
10108401478108401479TC16GENICheterozygous51772050
10108407879108407880AT36GENIChomozygous51596132
10108408887108408888TTC18GENICheterozygous51596134
10108408887108408888TTTC18GENICheterozygous51596136
10108409221108409222TTCA38GENICheterozygous51596138
10108409485108409486AG41GENIChomozygous51596140
10108410258108410259TA24GENIChomozygous51596142
10108411238108411239GA47GENIChomozygous51596144
10108411935108411936CT17GENICheterozygous51596146
10108412065108412066GA42GENIChomozygous51596148
10108412067108412068CCT42GENIChomozygous51596149
10108412524108412525CT42GENIChomozygous51596151
10108412774108412775TC44GENIChomozygous51596153