chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214611218214611219GC37GENICpossibly homozygous108532480
1214611257214611258CG35GENIChomozygous108532481
1214611273214611274GT35GENIChomozygous108532482
1214611700214611701GA162GENICheterozygous108532483
1214613150214613151AG250GENICheterozygous108532484
1214613253214613254CT237GENIChomozygous108532485
1214614780214614781CT39GENICpossibly homozygous108532486
1214616316214616317TG44GENIChomozygous108532487
1214616426214616427GA34GENIChomozygous108532488
1214618946214618947GA33GENIChomozygous108532490
1214621090214621091AG38GENIChomozygous108532491
1214625456214625457TC17GENIChomozygous108532492
1214625508214625509CT23GENICpossibly homozygous108532493
1214626396214626397GA32GENIChomozygous108532494
1214627682214627683CT22GENIChomozygous108532495
1214628089214628090TG13GENIChomozygous108532498
1214628090214628091TC14GENIChomozygous108532499
1214628823214628824TC27GENIChomozygous108532500
1214629338214629339GA32GENIChomozygous108532501
1214629427214629428CG39GENIChomozygous108532502
1214630231214630232TG39GENIChomozygous108532503