chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT9GENIChomozygous828326692
99073349690733497GGT18GENIChomozygous828326693
99073603090736031TTGGGA8GENIChomozygous828326694
99073603290736033TG8GENIChomozygous828326695
99073639590736396TG13GENICheterozygous828326696
99073693290736933TG7GENIChomozygous828326697
99073694690736947AG10GENIChomozygous828326698
99073695490736955TG8GENIChomozygous828326699
99073697190736972TA10GENIChomozygous828326700
99073748890737489TC15GENICheterozygous828326701
99073838490738385CT12GENIChomozygous828326702
99073856290738563TC9GENIChomozygous828326703
99073860890738609GA9GENIChomozygous828326704
99073864990738650CT7GENIChomozygous828326705
99074061090740612AT--12GENICheterozygous828326706
99074067290740673CT11GENIChomozygous828326707
99074164490741645AG11GENIChomozygous828326708
99074166290741663TC10GENIChomozygous828326709
99074258390742584CT7GENIChomozygous828326710
99074258590742586TC7GENIChomozygous828326711
99074259990742600CA7GENIChomozygous828326712
99074260190742602GT7GENIChomozygous828326713
99074260490742606CC--7GENIChomozygous828326714
99074261090742611CT7GENIChomozygous828326715
99074261190742612CA7GENIChomozygous828326716
99074293790742938CG11GENIChomozygous828326717
99074294190742943AG--11GENIChomozygous828326718
99074294590742946AAGG11GENIChomozygous828326719
99074296990742970GA14GENIChomozygous828326720
99074298290742983CT12GENIChomozygous828326721
99074300390743004GA8GENIChomozygous828326722
99074301090743011GA8GENIChomozygous828326723
99074472790744728CT8GENICheterozygous828326724
99074558690745587TG15GENICheterozygous828326725
99074741590747416CT15GENICheterozygous828326726
99074743390747434GA15GENICheterozygous828326727
99074751590747518GTA---15GENICheterozygous828326728
99074752190747524GTT---12GENICheterozygous828326729
99074803190748032CT7GENIChomozygous828326730
99074879190748792GGT16GENICheterozygous828326731