chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109106652691066527GGA23GENIChomozygous687879310
109106669591066696CT26GENIChomozygous515101471
109106671791066718GA25GENIChomozygous512175234
109106677791066778AG30GENIChomozygous515101472
109106678391066784GA28GENIChomozygous515101473
109106709091067091GA19GENIChomozygous515101474
109106747491067476CT--16GENIChomozygous687879311
109106778791067788TC28GENIChomozygous515101475
109106818591068186AAT16GENICpossibly homozygous687879312
109106910291069103TC33GENIChomozygous515101476
109106943891069440GG--9GENIChomozygous687879313
109106951591069516GA8GENIChomozygous515101477
109106960591069606CT16GENIChomozygous515101478
109106967291069673GA21GENIChomozygous515101479
109106973291069733AG25GENIChomozygous512175235
109106982491069825G-13GENIChomozygous687879315
109107006591070066GA19GENICpossibly homozygous515101480
109107011791070131GAGAGAGAGAGAGA--------------11GENIChomozygous687879317
109107013091070131A-21GENICheterozygous687879318
109107033491070335CG34GENIChomozygous512175236
109107058391070584AC28GENICpossibly homozygous515101481
109107102291071023AG16GENIChomozygous515101482
109107103591071036GA15GENIChomozygous515101483
109107210391072104GGTATT2GENIChomozygous687879319
109107222391072224T-9GENICpossibly homozygous687879322
109107268491072685A-1GENIChomozygous687879323
109107285291072853AG17GENIChomozygous515101484
109107286591072866CA18GENIChomozygous512175237