chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140448698140448698CGTA40GENIChomozygous128529072
7140448828140448830AC48GENIChomozygous128529073
7140449138140449139AG57GENICpossibly homozygous115938696
7140450582140450583AG37GENIChomozygous115938697
7140450993140450994AG55GENIChomozygous115938698
7140451011140451012CT55GENIChomozygous115938699
7140455199140455200CT51GENIChomozygous115938700
7140456602140456603GA64GENIChomozygous115938701
7140457165140457219CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCC20GENIChomozygous128529074
7140457575140457576AG46GENIChomozygous115938702
7140457607140457608AC40GENICpossibly homozygous115938703
7140457695140457696TA44GENIChomozygous115938704
7140457831140457832GT50GENIChomozygous115938705
7140458043140458061CCTGTGCTGTCTCTCCAG53GENIChomozygous128529075
7140458146140458147CT54GENIChomozygous115938706
7140458171140458172GA56GENIChomozygous115938707
7140458485140458486GC25GENIChomozygous115938708
7140458845140458845T17GENIChomozygous128529076
7140458879140458880TC23GENIChomozygous115938709
7140458893140458894GA30GENIChomozygous115938710
7140460127140460128TC43GENIChomozygous115938711
7140460500140460501AG43GENIChomozygous115938712
7140460871140460871A43GENIChomozygous128529077
7140454310140454311AC16GENICheterozygous130359607
7140454315140454316AC17GENICheterozygous130359608
7140462086140462087TA24GENIChomozygous115938714
7140462441140462442CT57GENIChomozygous115938715
7140462922140462923GC43GENIChomozygous115938716
7140463441140463442TC38GENIChomozygous115938717
7140465828140465832GGTG58GENIChomozygous128529078
7140465585140465586CT62GENIChomozygous115938720
7140465355140465356CT69GENIChomozygous115938718
7140465548140465549GT54GENIChomozygous115938719