chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT5GENIChomozygous742779246
99073349690733497GGT6GENIChomozygous742779247
99073384490733846GT--9GENICheterozygous742779249
99073588190735882AAGT8GENICheterozygous742779252
99073603090736031TTGGGA15GENIChomozygous742779255
99073603290736033TG15GENIChomozygous619083382
99073687890736879TG14GENIChomozygous619083383
99073692190736922TG14GENIChomozygous619083384
99073693290736933TG19GENIChomozygous619083385
99073694690736947AG23GENIChomozygous619083386
99073695490736955TG20GENIChomozygous619083387
99073697190736972TA15GENIChomozygous619083388
99073856290738563TC22GENIChomozygous619083389
99073880190738802C-4GENIChomozygous742779256
99073881790738818T-5GENIChomozygous742779257
99074145590741456AAAGG12GENIChomozygous742779258
99074258390742584CT11GENIChomozygous619083390
99074258590742586TC12GENIChomozygous619083391
99074259990742600CA14GENIChomozygous619083392
99074260190742602GT14GENIChomozygous619083393
99074260490742606CC--15GENIChomozygous742779259
99074261090742611CT18GENIChomozygous619083394
99074261190742612CA18GENIChomozygous619083395
99074294190742943AG--3GENIChomozygous742779260
99074294590742946AAGG3GENIChomozygous742779261
99074769090747691TTAG12GENIChomozygous742779262
99074795090747951CT13GENIChomozygous619083396