chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149003030149003031T52GENICpossibly homozygous136920772
4149003064149003064A44GENICpossibly homozygous136920773
4149004684149004685GA56GENIChomozygous137230076
4149005248149005249CT66GENIChomozygous137230077
4149007722149007723AG61GENIChomozygous137230078
4149008178149008179TC62GENIChomozygous137230079
4149008804149008805TC74GENICpossibly homozygous137230080
4149008807149008808TA74GENICpossibly homozygous137230081
4149009019149009020TC60GENIChomozygous137230082
4149009020149009021CT60GENIChomozygous137230083
4149010686149010687AG76GENIChomozygous137230084
4149011082149011083AG47GENIChomozygous137230085
4149011448149011448G20GENICheterozygous136920774
4149011707149011708CT51GENIChomozygous137230086
4149014343149014343C34GENICpossibly homozygous136920775
4149014528149014529TC49GENIChomozygous137230087
4149015822149015823GA65GENIChomozygous137230088
4149016052149016053CT74GENIChomozygous137230089
4149016056149016057AG72GENIChomozygous137230090
4149016086149016087AG70GENIChomozygous137230091
4149016601149016602AG56GENIChomozygous137230092
4149016977149016977T57GENICpossibly homozygous136920776
4149018381149018382TC51GENIChomozygous137230093
4149018458149018459CG52GENIChomozygous137230094
4149018522149018523AG62GENIChomozygous137230095
4149018581149018582CA59GENIChomozygous137230096
4149018864149018865AC61GENIChomozygous137230097
4149018908149018909TC58GENICpossibly homozygous137230098
4149019229149019230TG61GENIChomozygous137230099
4149023455149023456GA63GENIChomozygous137230100
4149023561149023562TC63GENIChomozygous137230101
4149023598149023599TA61GENIChomozygous137230102
4149026063149026064AG75GENICpossibly homozygous137230103
4149026116149026117AG86GENIChomozygous137230104
4149029970149029970GA51GENIChomozygous136920777
4149035482149035483TC50GENIChomozygous137230105
4149039520149039521TC81GENIChomozygous137230107
4149042846149042847AC16GENIChomozygous137230108