chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1208608235208608236CT38GENICpossibly homozygous145321745
1208612303208612304CG45GENIChomozygous141298589
1208612772208612773AG54GENIChomozygous145321746
1208613059208613060TC41GENIChomozygous142858722
1208615262208615263CT18GENIChomozygous141298590
1208615634208615635TA48GENICpossibly homozygous141298591
1208615943208615944A51GENIChomozygous141179611
1208616714208616715CA67GENIChomozygous141298593
1208617049208617050AT59GENIChomozygous145321747
1208618026208618030TGTG55GENIChomozygous141179612
1208615929208615930T52GENIChomozygous145246145
1208618809208618829GAAAGAAAGAACAAACGAAC39GENIChomozygous145246146
1208618824208618825CA39GENICheterozygous403800760
1208618828208618829CA39GENICheterozygous403800762
1208618820208618821CA39GENICheterozygous403800758
1208618820208618821C39GENIChomozygous403800759
1208618824208618825C39GENIChomozygous403800761
1208618828208618829C39GENIChomozygous403800763
1208619252208619252G44GENIChomozygous141179613
1208619840208619841AC54GENIChomozygous141298595
1208619840208619840C53GENIChomozygous141179614
1208620102208620103AG60GENIChomozygous141298596
1208620213208620214GA49GENIChomozygous141298597