chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186227907162279072AG60GENIChomozygous980804807
186227971562279716TC31GENIChomozygous980804808
186228009062280091TC20GENICpossibly homozygous980804809
186228082462280825TC37GENIChomozygous980804810
186228105962281060GC17GENIChomozygous980804811
186228127862281279GA28GENIChomozygous980804812
186228139662281397CT30GENIChomozygous980804813
186228155862281559AG36GENIChomozygous980804814
186228160862281609AT47GENIChomozygous980804815
186228194162281942GT37GENIChomozygous980804816
186228198462281985TC37GENIChomozygous980804817
186228209162282092TC19GENIChomozygous980804818
186228694162286942TA31GENIChomozygous980804819
186228695062286951AG34GENIChomozygous980804820
186228711162287112TA37GENIChomozygous980804821
186228725762287258GA34GENIChomozygous980804822
186228727062287271CT35GENIChomozygous980804823
186228727462287275AG36GENIChomozygous980804824
186228730062287301TC43GENIChomozygous980804825