chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105557200055572001GA25GENIChomozygous116782662
105557240255572403CT27GENIChomozygous116782664
105557271855572719AG35GENIChomozygous116782666
105557307255573073AG31GENIChomozygous116934861
105557497655574977TA16GENIChomozygous116978011
105557579855575799CT34GENIChomozygous116602605
105557600455576005CG44GENIChomozygous117130674
105557627655576277AT31GENIChomozygous116602607
105557739355577394GA27GENIChomozygous117130675
105557768855577689GA48GENIChomozygous117130676
105557801755578018AG26GENIChomozygous116934871
105557834655578347AG34GENIChomozygous117130677
105557856655578567TG41GENIChomozygous117130678
105557907255579073CT36GENIChomozygous116602609
105558069455580695AC30GENIChomozygous117130679
105558141755581418AC35GENIChomozygous116602611
105558205055582051CT27GENIChomozygous117130680
105558254555582546TA33GENIChomozygous117130681
105558305555583056TC51GENIChomozygous116602613
105558348455583485AG34GENIChomozygous116602615
105558357955583580GA32GENIChomozygous117130682
105558520055585201AG27GENIChomozygous116602619
105558618055586181CT22GENIChomozygous117130683
105558661255586613AG21GENIChomozygous116602623
105558763555587636TC25GENIChomozygous116602625
105558798655587987TC28GENIChomozygous117130684
105558894455588945GT33GENIChomozygous117130685
105559043055590431CT32GENIChomozygous116602627
105559231555592316GA25GENIChomozygous117130686
105559240155592402GA18GENIChomozygous117130687
105559332055593321AG21GENIChomozygous117130688