chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1152099336152099337CA17GENICheterozygous132002857
1152099562152099563TC12GENICheterozygous132002859
1152099581152099582AG13GENICheterozygous121099396
1152099607152099608GT17GENICheterozygous121099397
1152099643152099644AG19GENICheterozygous121099398
1152104133152104134TG50GENICheterozygous108307838
1152104199152104201TC46GENICheterozygous132794534
1152104214152104215TG41GENICheterozygous108749414
1152142534152142535T31GENIChomozygous127446570
1152142535152142536GA32GENIChomozygous121099441
1152142544152142548CTTG31GENIChomozygous127446571
1152142552152142552CCAA32GENIChomozygous127446572
1152142554152142557TCT30GENIChomozygous127446573
1152142560152142560AT29GENIChomozygous127446574
1152142563152142564AC29GENIChomozygous121099446
1152142568152142569AT28GENIChomozygous121099447
1152142581152142582GA28GENIChomozygous109051557
1152142596152142597GA27GENIChomozygous109051559
1152142597152142598TC27GENIChomozygous109051560
1152142600152142601TC27GENIChomozygous109051561
1152142616152142617AT26GENIChomozygous121099448
1152142617152142618GT26GENIChomozygous121099449
1152142621152142622TC26GENIChomozygous121099450
1152142622152142623GA25GENIChomozygous121099451
1152142624152142625GA24GENIChomozygous121099452
1152142627152142628TC23GENIChomozygous121099453
1152142633152142634TC23GENIChomozygous130233611
1152142636152142637GA22GENIChomozygous121099455
1152142641152142642TC22GENIChomozygous121099456
1152142642152142643TA22GENIChomozygous121099457
1152142649152142650TC19GENIChomozygous109565211