chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094261264094262TC28GENICpossibly homozygous992765721
1264095002264095003TC31GENICpossibly homozygous992765722
1264095472264095473TC33GENIChomozygous992765723
1264095886264095887AG29GENICpossibly homozygous992765724
1264096218264096219CT36GENICpossibly homozygous992765725
1264096731264096732GA32GENIChomozygous992765726
1264097115264097116CT24GENIChomozygous992765727
1264097200264097201GA35GENICpossibly homozygous992765728
1264097208264097209TC35GENICpossibly homozygous992765729
1264097432264097433TC19GENIChomozygous992765730
1264097633264097634AC39GENIChomozygous992765731
1264098036264098037GT26GENICpossibly homozygous992765732
1264098042264098043GA25GENICpossibly homozygous992765733
1264098403264098404TC20GENIChomozygous992765734
1264098424264098425GA23GENIChomozygous992765735
1264099176264099177GA18GENICpossibly homozygous992765736
1264099576264099577CT11GENICpossibly homozygous992765737
1264099875264099876CT35GENICpossibly homozygous992765738
1264100059264100060TA27GENIChomozygous992765739
1264100188264100189AG23GENIChomozygous992765740
1264100212264100213TG20GENICpossibly homozygous992765741
1264100452264100453CA25GENICpossibly homozygous992765742
1264100637264100638TC36GENIChomozygous992765743
1264100695264100696GA35GENICpossibly homozygous992765744
1264101486264101487CG5GENIChomozygous992765745
1264103421264103422CT30GENIChomozygous992765746
1264105400264105401TG35GENICpossibly homozygous992765747
1264105443264105444AC26GENIChomozygous992765748