chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72413897624138977TC18GENIChomozygous54321137
72413913224139133TTA19GENICheterozygous53836430
72413913224139133TTAAAA19GENICheterozygous54321140
72413913224139133TTAA19GENICheterozygous55073079
72414080724140808AG29GENIChomozygous56151313
72414106324141064TC25GENIChomozygous54321179
72414129524141296AT24GENIChomozygous53836431
72414178824141789AG26GENIChomozygous53836432
72414194024141941AG23GENIChomozygous53836433
72414441224144413GT21GENICpossibly homozygous56151315
72414639224146393A-20GENICpossibly homozygous53836435
72414722124147223TT--19GENIChomozygous56151317
72414935124149352AAT7GENIChomozygous53836442
72415105124151052TC23GENIChomozygous54321468
72415220824152209G-20GENIChomozygous56151319
72415282024152821TC32GENICpossibly homozygous54321499
72415343224153433CG17GENIChomozygous54718394
72415431724154318TC35GENIChomozygous54321516
72415448024154481GT23GENIChomozygous54718396
72415459624154597GA28GENIChomozygous53836446
72415480324154804CG31GENIChomozygous54321525
72415484624154847AG27GENIChomozygous54321528
72415014524150146CT17GENIChomozygous54887112