chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214611218214611219GC13GENIChomozygous108532480
1214611257214611258CG12GENIChomozygous108532481
1214611273214611274GT12GENIChomozygous108532482
1214611700214611701GA32GENICheterozygous108532483
1214613150214613151AG109GENICheterozygous108532484
1214613253214613254CT144GENIChomozygous108532485
1214614780214614781CT12GENIChomozygous108532486
1214616316214616317TG14GENIChomozygous108532487
1214616426214616427GA17GENIChomozygous108532488
1214618946214618947GA20GENIChomozygous108532490
1214621090214621091AG19GENIChomozygous108532491
1214625456214625457TC21GENIChomozygous108532492
1214625508214625509CT19GENIChomozygous108532493
1214626396214626397GA22GENIChomozygous108532494
1214627682214627683CT17GENIChomozygous108532495
1214627964214627965CT7GENIChomozygous121174459
1214628089214628090TG13GENIChomozygous108532498
1214628090214628091TC13GENIChomozygous108532499
1214628823214628824TC15GENIChomozygous108532500
1214629338214629339GA31GENIChomozygous108532501
1214629427214629428CG23GENIChomozygous108532502
1214630231214630232TG17GENIChomozygous108532503
1214629595214629599CTAA24GENIChomozygous127481197