chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214609731214609732GA12GENIChomozygous120592318
1214611218214611219GC12GENIChomozygous108532480
1214611273214611274GT7GENIChomozygous108532482
1214611700214611701GA34GENICheterozygous108532483
1214612842214612843TG22GENICheterozygous134396124
1214613227214613228GA85GENICheterozygous108990464
1214613242214613243CG79GENICheterozygous108990465
1214613253214613254CT75GENIChomozygous108532485
1214614780214614781CT19GENIChomozygous108532486
1214615174214615175GA4GENICheterozygous134396126
1214616316214616317TG24GENIChomozygous108532487
1214617464214617465CT18GENIChomozygous125438154
1214620883214620884GA16GENIChomozygous125438155
1214625456214625457TC10GENIChomozygous108532492
1214625549214625550TA15GENIChomozygous125438156
1214627964214627965CT23GENIChomozygous121174459
1214628089214628090TG18GENIChomozygous108532498
1214628090214628091TC18GENIChomozygous108532499
1214628823214628824TC22GENIChomozygous108532500
1214629427214629428CG20GENIChomozygous108532502
1214630319214630320GA24GENIChomozygous125438158