chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106361612763616128TG10GENIChomozygous51672433
106361694863616949AATT6GENIChomozygous52440520
106361762763617628AG19GENIChomozygous52250067
106361788863617889GGTTTGT11GENIChomozygous51672443
106361821263618213AT25GENIChomozygous52250069
106361867963618680TA24GENIChomozygous52250071
106361956363619564CG16GENIChomozygous51475133
106362006563620066GA20GENIChomozygous52250073
106362160663621607GA6GENIChomozygous52250076
106362211763622118AC22GENIChomozygous51475138
106362213863622139AG28GENIChomozygous51672454
106362308263623083GGA15GENIChomozygous52250078
106362434063624341CT8GENIChomozygous52250080
106362604763626048TG30GENIChomozygous51672456
106362661063626611GA29GENIChomozygous52250082
106362681863626819AG26GENIChomozygous51475140
106362708563627086AT23GENIChomozygous52250084
106362742463627425AG31GENIChomozygous52250086
106362857663628577TG23GENIChomozygous51672464
106363040963630410GGT11GENIChomozygous51475142
106363073963630740AG19GENIChomozygous52250090
106363074963630750GC17GENIChomozygous52250092
106363094063630941CT19GENIChomozygous52250094
106363149763631498GA15GENIChomozygous52250096
106363195063631951GT20GENIChomozygous51475143
106363207063632071TG15GENICpossibly homozygous51672468
106363312963633130GA18GENIChomozygous52250098
106363332863633329AG25GENIChomozygous52250100
106363339763633398AAG24GENIChomozygous51475146