chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
394431049443105TC9GENIChomozygous57142628
394431759443176G-19GENIChomozygous57142630
394441739444174GGTCC23GENIChomozygous57142632
394453499445350CA14GENIChomozygous59995104
394455399445540GA22GENIChomozygous59757586
394467099446710AG34GENICpossibly homozygous57142636
394467969446797AG16GENIChomozygous57142638
394471069447107TA20GENIChomozygous57142640
394477319447732TC37GENIChomozygous57142644
394479159447916TC14GENIChomozygous59995105
394481499448150CT18GENIChomozygous59995106
394482629448263AAC1GENIChomozygous58412535
394486189448619GGGGC29GENICpossibly homozygous57142650
394489189448919C-22GENIChomozygous59995107
394494119449412CT27GENICpossibly homozygous59995108
394495979449598GT34GENICpossibly homozygous59995109
394499579449958CT14GENIChomozygous57142652
394506239450624CT16GENICpossibly homozygous57142654
394476109447614TGTG----5GENIChomozygous59465249
394480379448038CCT7GENICpossibly homozygous58637462
394486159448617TT--29GENICpossibly homozygous59036644
394486169448617TTAGGGA29GENICpossibly homozygous59036646
394497809449781GA24GENIChomozygous59826156