chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT14GENIChomozygous938205728
5159590355159590356AC19GENIChomozygous938205729
5159590356159590357GC19GENIChomozygous938205730
5159590516159590517AG21GENIChomozygous938205731
5159590543159590544TC22GENIChomozygous938205732
5159590810159590811GA35GENIChomozygous938205733
5159591165159591166AG28GENIChomozygous938205734
5159591294159591295GA12GENIChomozygous938205735
5159591492159591493CT18GENIChomozygous938205736
5159591711159591712GA19GENIChomozygous938205737
5159591959159591960CT24GENIChomozygous938205738
5159592241159592242AG26GENIChomozygous938205739
5159592551159592552GA29GENIChomozygous938205740
5159592713159592714CT15GENIChomozygous938205741
5159592986159592987CT16GENIChomozygous938205742
5159593011159593012TA16GENIChomozygous938205743
5159593229159593230AG22GENIChomozygous938205744
5159593316159593317AC27GENIChomozygous938205745
5159594085159594086GA22GENIChomozygous938205746
5159594458159594459TG30GENIChomozygous938205747
5159594550159594551CT20GENIChomozygous938205748
5159596985159596986CT14GENIChomozygous938205749
5159599212159599213CT19GENIChomozygous938205750
5159599504159599505TC5GENIChomozygous938205751
5159599790159599791GC17GENIChomozygous938205752
5159599908159599909TG22GENIChomozygous938205753
5159600471159600472TC13GENIChomozygous938205754
5159600745159600746AC15GENIChomozygous938205755
5159600747159600748GT16GENIChomozygous938205756
5159600839159600840CT26GENIChomozygous938205757
5159600968159600969AG20GENIChomozygous938205758
5159601143159601144CT25GENIChomozygous938205759
5159601217159601218AG24GENIChomozygous938205760
5159601274159601275AG29GENIChomozygous938205761
5159601408159601409TC17GENIChomozygous938205762
5159602018159602019CT13GENIChomozygous938205763