chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094261264094262TC21GENIChomozygous891587735
1264095002264095003TC15GENIChomozygous891587736
1264095472264095473TC17GENIChomozygous891587737
1264095886264095887AG10GENIChomozygous891587738
1264096218264096219CT9GENIChomozygous891587739
1264096731264096732GA14GENIChomozygous891587740
1264097079264097080AT10GENICheterozygous891587741
1264097115264097116CT21GENIChomozygous891587742
1264097432264097433TC11GENIChomozygous891587743
1264097633264097634AC24GENIChomozygous891587744
1264098036264098037GT11GENIChomozygous891587745
1264098042264098043GA11GENIChomozygous891587746
1264098403264098404TC8GENIChomozygous891587747
1264098424264098425GA5GENIChomozygous891587748
1264099176264099177GA4GENIChomozygous891587749
1264099576264099577CT28GENIChomozygous891587750
1264099875264099876CT19GENIChomozygous891587751
1264100059264100060TA16GENIChomozygous891587752
1264100188264100189AG14GENICheterozygous891587753
1264100212264100213TG6GENICheterozygous891587754
1264100452264100453CA18GENIChomozygous891587755
1264100637264100638TC23GENIChomozygous891587756
1264100695264100696GA14GENIChomozygous891587757
1264101486264101487CG6GENIChomozygous891587758
1264103421264103422CT15GENIChomozygous891587759
1264105170264105171CT12GENIChomozygous891587760
1264105400264105401TG15GENIChomozygous891587761
1264105443264105444AC7GENIChomozygous891587762