chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214611218214611219GC31GENIChomozygous108532480
1214611257214611258CG22GENIChomozygous108532481
1214611273214611274GT22GENIChomozygous108532482
1214611700214611701GA177GENICheterozygous108532483
1214613150214613151AG249GENICheterozygous108532484
1214613253214613254CT249GENIChomozygous108532485
1214614780214614781CT41GENIChomozygous108532486
1214616316214616317TG30GENIChomozygous108532487
1214616426214616427GA15GENIChomozygous108532488
1214618946214618947GA46GENIChomozygous108532490
1214621090214621091AG27GENIChomozygous108532491
1214623048214623049AG42GENICheterozygous109448923
1214625456214625457TC34GENIChomozygous108532492
1214625508214625509CT30GENIChomozygous108532493
1214626396214626397GA20GENIChomozygous108532494
1214627682214627683CT42GENIChomozygous108532495
1214627976214627977CT38GENICheterozygous108532496
1214627978214627979CT38GENICheterozygous108532497
1214628089214628090TG24GENIChomozygous108532498
1214628090214628091TC22GENIChomozygous108532499
1214628823214628824TC35GENIChomozygous108532500
1214629338214629339GA27GENIChomozygous108532501
1214629427214629428CG41GENIChomozygous108532502
1214630231214630232TG38GENIChomozygous108532503