chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140450066140450067AC30GENIChomozygous134708148
7140450582140450583AG45GENIChomozygous115938697
7140450936140450937AG37GENIChomozygous134708149
7140453209140453210CT61GENIChomozygous134708150
7140455276140455277CT51GENIChomozygous134708151
7140455883140455884TG17GENIChomozygous134708152
7140456602140456603GA56GENIChomozygous115938701
7140457575140457576AG40GENIChomozygous115938702
7140457695140457696TA33GENIChomozygous115938704
7140457831140457832GT57GENIChomozygous115938705
7140458146140458147CT49GENIChomozygous115938706
7140454310140454311AC17GENICheterozygous130359607
7140454315140454316AC18GENICheterozygous130359608
7140454326140454327AC18GENICheterozygous130359609
7140454816140454817CG54GENIChomozygous118287429
7140458171140458172GA46GENIChomozygous115938707
7140458485140458486GC36GENIChomozygous115938708
7140458879140458880TC33GENIChomozygous115938709
7140458893140458894GA33GENIChomozygous115938710
7140459203140459204TC29GENIChomozygous118515593
7140460500140460501AG27GENIChomozygous115938712
7140460671140460672AT48GENIChomozygous118515594
7140462243140462244CG43GENIChomozygous134708153
7140462922140462923GC35GENIChomozygous115938716
7140463149140463150TC35GENIChomozygous118515595
7140463441140463442TC34GENIChomozygous115938717
7140464949140464950GA52GENIChomozygous134708154
7140465402140465403CT59GENICpossibly homozygous118515596
7140459432140459434TG30GENICheterozygous129939984
7140453362140453362G57GENIChomozygous134704014
7140455877140455878T17GENIChomozygous134704015
7140455880140455881T17GENIChomozygous134704016
7140458845140458845T26GENIChomozygous128529076
7140461900140461902TG29GENIChomozygous134704017
7140462029140462029T22GENICheterozygous134704018
7140464776140464777G33GENIChomozygous132985660