chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145119351145119352AG17GENIChomozygous115946571
7145120078145120079TG22GENIChomozygous115946573
7145120692145120693CA27GENIChomozygous115946575
7145120839145120840CT22GENIChomozygous115946577
7145121171145121172TC13GENIChomozygous115946580
7145121810145121811TG21GENIChomozygous115946582
7145121814145121815TC20GENIChomozygous115946584
7145121834145121835CG16GENIChomozygous115946586
7145121967145121968GT16GENIChomozygous115946588
7145122094145122095GA18GENIChomozygous115946590
7145124175145124176AG16GENIChomozygous115946593
7145124844145124845GA12GENIChomozygous115946595
7145125788145125789AG21GENIChomozygous115946597
7145125874145125875GA22GENIChomozygous115946599
7145126437145126438GA14GENIChomozygous115946601
7145129161145129162AG9GENIChomozygous115946605
7145130840145130841TG9GENICheterozygous118391163
7145130955145130956GA16GENIChomozygous115946607
7145131424145131425GA16GENIChomozygous115946609
7145135727145135728GA15GENICpossibly homozygous115946613
7145136230145136231GA20GENIChomozygous115946614
7145145016145145017CT15GENIChomozygous115946616