chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105557579855575799CT26GENIChomozygous116602605
105557627655576277AT26GENIChomozygous116602607
105557739355577394GA35GENIChomozygous117130675
105557768855577689GA32GENIChomozygous117130676
105557801755578018AG14GENIChomozygous116934871
105557834655578347AG28GENIChomozygous117130677
105557856655578567TG22GENIChomozygous117130678
105557907255579073CT19GENIChomozygous116602609
105558069455580695AC38GENIChomozygous117130679
105558141755581418AC21GENIChomozygous116602611
105558205055582051CT30GENIChomozygous117130680
105558254555582546TA23GENIChomozygous117130681
105558305555583056TC27GENIChomozygous116602613
105558348455583485AG33GENIChomozygous116602615
105558357955583580GA25GENIChomozygous117130682
105558520055585201AG21GENIChomozygous116602619
105558618055586181CT27GENIChomozygous117130683
105558661255586613AG29GENIChomozygous116602623
105558763555587636TC25GENIChomozygous116602625
105558798655587987TC31GENIChomozygous117130684
105558894455588945GT26GENIChomozygous117130685
105559043055590431CT32GENIChomozygous116602627
105559231555592316GA35GENIChomozygous117130686
105559240155592402GA35GENIChomozygous117130687
105559271655592717AT5GENIChomozygous116602629
105559332055593321AG27GENIChomozygous117130688