chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140449138140449139AG15GENIChomozygous115938696
7140450582140450583AG6GENIChomozygous115938697
7140450993140450994AG20GENIChomozygous115938698
7140451011140451012CT16GENIChomozygous115938699
7140455199140455200CT7GENIChomozygous115938700
7140455949140455950CT4GENICheterozygous126620861
7140455967140455968TA4GENICheterozygous126620862
7140456602140456603GA13GENIChomozygous115938701
7140457575140457576AG20GENIChomozygous115938702
7140457607140457608AC12GENIChomozygous115938703
7140457695140457696TA17GENIChomozygous115938704
7140457831140457832GT11GENIChomozygous115938705
7140458146140458147CT22GENIChomozygous115938706
7140458171140458172GA24GENIChomozygous115938707
7140458485140458486GC5GENICheterozygous115938708
7140458879140458880TC20GENIChomozygous115938709
7140458893140458894GA8GENIChomozygous115938710
7140460127140460128TC24GENIChomozygous115938711
7140460500140460501AG16GENIChomozygous115938712
7140462086140462087TA11GENIChomozygous115938714
7140463441140463442TC4GENIChomozygous115938717
7140465355140465356CT4GENIChomozygous115938718
7140465548140465549GT14GENIChomozygous115938719
7140465585140465586CT14GENIChomozygous115938720
7140465830140465831TC5GENIChomozygous126620863
7140465831140465832GA4GENICheterozygous126620864