chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145118052145118053GA23GENIChomozygous115946569
7145119351145119352AG22GENIChomozygous115946571
7145120078145120079TG17GENIChomozygous115946573
7145120692145120693CA8GENIChomozygous115946575
7145120839145120840CT11GENIChomozygous115946577
7145121810145121811TG19GENIChomozygous115946582
7145121814145121815TC19GENIChomozygous115946584
7145121834145121835CG17GENIChomozygous115946586
7145121967145121968GT25GENIChomozygous115946588
7145122094145122095GA18GENIChomozygous115946590
7145123742145123743AT21GENIChomozygous115946591
7145124844145124845GA22GENIChomozygous115946595
7145125788145125789AG24GENIChomozygous115946597
7145125874145125875GA19GENIChomozygous115946599
7145126437145126438GA23GENIChomozygous115946601
7145128606145128607TC4GENIChomozygous115946603
7145130955145130956GA27GENIChomozygous115946607
7145131424145131425GA14GENIChomozygous115946609
7145136230145136231GA23GENIChomozygous115946614
7145136826145136827AG19GENIChomozygous116378455
7145135852145135853AT19GENIChomozygous116378453