chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214611218214611219GC32GENIChomozygous108532480
1214611273214611274GT31GENICpossibly homozygous108532482
1214616316214616317TG20GENIChomozygous108532487
1214616426214616427GA25GENIChomozygous108532488
1214618946214618947GA18GENIChomozygous108532490
1214621090214621091AG27GENIChomozygous108532491
1214625456214625457TC24GENIChomozygous108532492
1214625508214625509CT26GENIChomozygous108532493
1214626396214626397GA26GENICpossibly homozygous108532494
1214627682214627683CT18GENICpossibly homozygous108532495
1214628089214628090TG25GENIChomozygous108532498
1214628090214628091TC25GENIChomozygous108532499
1214628823214628824TC19GENIChomozygous108532500
1214629338214629339GA20GENIChomozygous108532501
1214629427214629428CG24GENIChomozygous108532502
1214630231214630232TG9GENIChomozygous108532503