chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140448698140448698CGTA30GENIChomozygous128529072
7140448828140448830AC35GENIChomozygous128529073
7140449138140449139AG50GENIChomozygous115938696
7140450582140450583AG40GENIChomozygous115938697
7140450993140450994AG52GENIChomozygous115938698
7140451011140451012CT48GENIChomozygous115938699
7140455199140455200CT36GENIChomozygous115938700
7140456602140456603GA39GENIChomozygous115938701
7140457165140457219CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCC10GENIChomozygous128529074
7140457575140457576AG32GENIChomozygous115938702
7140457607140457608AC32GENIChomozygous115938703
7140457695140457696TA35GENIChomozygous115938704
7140457831140457832GT43GENIChomozygous115938705
7140458043140458061CCTGTGCTGTCTCTCCAG30GENIChomozygous128529075
7140458146140458147CT27GENIChomozygous115938706
7140458171140458172GA33GENIChomozygous115938707
7140458485140458486GC25GENIChomozygous115938708
7140458845140458845T17GENIChomozygous128529076
7140458879140458880TC17GENIChomozygous115938709
7140458893140458894GA18GENIChomozygous115938710
7140460127140460128TC46GENIChomozygous115938711
7140460500140460501AG45GENIChomozygous115938712
7140460871140460871A37GENIChomozygous128529077
7140462086140462087TA20GENIChomozygous115938714
7140462441140462442CT42GENIChomozygous115938715
7140462922140462923GC46GENIChomozygous115938716
7140463441140463442TC39GENIChomozygous115938717
7140465355140465356CT49GENIChomozygous115938718
7140465548140465549GT40GENIChomozygous115938719
7140465585140465586CT37GENIChomozygous115938720
7140465828140465832GGTG48GENIChomozygous128529078