chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106361612763616128TG40GENIChomozygous573520154
106361694863616949AATT14GENIChomozygous712974099
106361762763617628AG27GENIChomozygous575275576
106361788863617889GGTTTGT24GENIChomozygous712974101
106361821263618213AT23GENIChomozygous575275577
106361867963618680TA19GENIChomozygous575275578
106361956363619564CG23GENIChomozygous575275579
106362006563620066GA23GENIChomozygous575275580
106362160663621607GA1GENIChomozygous575275581
106362211763622118AC26GENIChomozygous573520155
106362213863622139AG29GENIChomozygous573520156
106362308263623083GGA18GENIChomozygous712974102
106362434063624341CT15GENIChomozygous575275582
106362604763626048TG24GENIChomozygous573520157
106362661063626611GA20GENIChomozygous575275583
106362681863626819AG29GENIChomozygous575275584
106362708563627086AT26GENIChomozygous575275585
106362742463627425AG16GENIChomozygous575275586
106362857663628577TG17GENIChomozygous573520158
106363040963630410GGT3GENIChomozygous712974103
106363073963630740AG13GENIChomozygous575275587
106363074963630750GC16GENIChomozygous575275588
106363094063630941CT20GENIChomozygous575275589
106363149763631498GA13GENIChomozygous575275590
106363195063631951GT19GENIChomozygous573520159
106363207063632071TG19GENIChomozygous573520160
106363312963633130GA17GENIChomozygous573520161
106363332863633329AG8GENIChomozygous573520162
106363339763633398AAG12GENIChomozygous712974104