chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
826810222681023TA15GENICpossibly homozygous671232603
826819802681981TG14GENICpossibly homozygous671232604
826824252682426TG22GENICpossibly homozygous671232605
826827532682754T-3GENICheterozygous768973117
826831832683184CT17GENICheterozygous671232606
826839712683972TC13GENIChomozygous671232607
826840892684090TG7GENIChomozygous671232608
826843192684320CT13GENIChomozygous671232609
826844202684421GA2GENIChomozygous671232610
826850182685019CT6GENIChomozygous671232611
826864892686490CG4GENIChomozygous671232612
826884522688453T-5GENICheterozygous768973118
826890492689050CCT2GENICheterozygous768973119
826890642689069TTTTT-----1GENIChomozygous768973121
826893082689309TC9GENIChomozygous671232613
826902662690267CT17GENIChomozygous671232614
826936382693639G-2GENIChomozygous768973123
826941252694126C-1GENIChomozygous768973124
826944932694494CT6GENICheterozygous671232615
826946482694649AAT1GENIChomozygous768973125
826953212695322CG4GENICheterozygous671232616
826959492695950GA2GENICheterozygous671232617
826970242697025CA9GENIChomozygous671232618
826979702697971TA3GENIChomozygous671232619
827004192700420CT20GENICheterozygous671232620
827013902701391GA24GENICpossibly homozygous671232621
827026552702656GGT4GENICheterozygous768973126
827040642704065AT19GENICpossibly homozygous671232622
827069982706999TC15GENICpossibly homozygous671232623
827079192707920T-1GENIChomozygous768973127
827080192708020A-8GENIChomozygous768973128
827086492708650A-1GENIChomozygous768973129
827091772709178TA10GENIChomozygous671232624
827112932711294CT14GENIChomozygous671232625