chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214609731214609732GA20GENIChomozygous120592318
1214611172214611173AG30GENIChomozygous120592320
1214611218214611219GC28GENIChomozygous108532480
1214611273214611274GT32GENIChomozygous108532482
1214615891214615892TC24GENIChomozygous120592322
1214616186214616187TA31GENIChomozygous120592324
1214616316214616317TG31GENIChomozygous108532487
1214616426214616427GA37GENIChomozygous108532488
1214618501214618502AG32GENIChomozygous120592326
1214620161214620162CT26GENIChomozygous120592328
1214620206214620207GA25GENIChomozygous120592330
1214621601214621602TC22GENIChomozygous108990468
1214623317214623318GT35GENIChomozygous120592332
1214625451214625452GA19GENIChomozygous120592334
1214625456214625457TC20GENIChomozygous108532492
1214628089214628090TG29GENIChomozygous108532498
1214628090214628091TC29GENIChomozygous108532499
1214628823214628824TC22GENIChomozygous108532500
1214629427214629428CG32GENIChomozygous108532502