chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140449138140449139AG19GENIChomozygous115938696
7140450582140450583AG11GENIChomozygous115938697
7140450993140450994AG21GENIChomozygous115938698
7140451011140451012CT18GENIChomozygous115938699
7140455199140455200CT26GENIChomozygous115938700
7140456602140456603GA22GENIChomozygous115938701
7140457174140457175TC3GENICheterozygous116096858
7140457575140457576AG9GENIChomozygous115938702
7140457607140457608AC20GENIChomozygous115938703
7140457831140457832GT8GENIChomozygous115938705
7140458146140458147CT27GENIChomozygous115938706
7140458171140458172GA26GENIChomozygous115938707
7140458879140458880TC11GENIChomozygous115938709
7140458893140458894GA12GENIChomozygous115938710
7140460127140460128TC23GENIChomozygous115938711
7140460500140460501AG12GENIChomozygous115938712
7140463441140463442TC4GENIChomozygous115938717
7140465355140465356CT17GENIChomozygous115938718
7140465548140465549GT22GENIChomozygous115938719
7140465585140465586CT19GENIChomozygous115938720