chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214611218214611219GC16GENIChomozygous108532480
1214611257214611258CG15GENIChomozygous108532481
1214611273214611274GT11GENIChomozygous108532482
1214611700214611701GA35GENICheterozygous108532483
1214613150214613151AG126GENICheterozygous108532484
1214613253214613254CT180GENIChomozygous108532485
1214614780214614781CT10GENIChomozygous108532486
1214616316214616317TG21GENIChomozygous108532487
1214616426214616427GA24GENIChomozygous108532488
1214618946214618947GA23GENIChomozygous108532490
1214621090214621091AG27GENIChomozygous108532491
1214625456214625457TC21GENIChomozygous108532492
1214625508214625509CT21GENIChomozygous108532493
1214626396214626397GA29GENIChomozygous108532494
1214627682214627683CT24GENIChomozygous108532495
1214627964214627965CT15GENIChomozygous121174459
1214628089214628090TG26GENIChomozygous108532498
1214628090214628091TC26GENIChomozygous108532499
1214628823214628824TC36GENIChomozygous108532500
1214629338214629339GA33GENIChomozygous108532501
1214629427214629428CG35GENIChomozygous108532502
1214630231214630232TG26GENIChomozygous108532503
1214629595214629599CTAA27GENIChomozygous127481197