chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119554728119554729AG26GENIChomozygous115852485
7119554834119554835CG27GENIChomozygous115852487
7119555210119555211CT52GENIChomozygous116302606
7119555397119555398TC33GENIChomozygous115852489
7119555404119555405GA31GENIChomozygous116302607
7119555406119555407CT30GENIChomozygous115852491
7119555501119555502GA33GENICpossibly homozygous115852493
7119555624119555625AG25GENIChomozygous115852495
7119556868119556869GA46GENIChomozygous116302608
7119557185119557186GT15GENIChomozygous115852521
7119558718119558719AT42GENIChomozygous116302609
7119558739119558740AG46GENIChomozygous116302610
7119558755119558756AG50GENIChomozygous115852535
7119559502119559503CT32GENIChomozygous116302611
7119561740119561741GA42GENIChomozygous116302612
7119561908119561909AT29GENIChomozygous116302613
7119563679119563680TC42GENIChomozygous116302614
7119564219119564220AG25GENIChomozygous116302615
7119565317119565318CT41GENIChomozygous116302616
7119565389119565390GA32GENIChomozygous116302617
7119565653119565654CT48GENIChomozygous116302618
7119565918119565919GA38GENIChomozygous116302619
7119565957119565958GA36GENIChomozygous116302620
7119566004119566005TC40GENIChomozygous116302621
7119566041119566042AG32GENIChomozygous116302622
7119566528119566529CT38GENIChomozygous116302623
7119566613119566614AG37GENIChomozygous116302624
7119566637119566638TA42GENIChomozygous116302625
7119566822119566823GA50GENICpossibly homozygous116302626
7119567839119567840TC33GENIChomozygous115852577