chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103145369931453700GT9GENIChomozygous116546580
103145371131453712AG10GENIChomozygous116546582
103145372231453723AG10GENIChomozygous116546584
103145373731453738AG10GENIChomozygous116546586
103146206031462061TC7GENIChomozygous116546588
103146501431465015GT9GENIChomozygous116546590
103146504831465049CG11GENIChomozygous116546592
103146505031465051GT11GENIChomozygous116546594
103146540031465401AC9GENIChomozygous116546596
103146545731465458GT10GENIChomozygous116546598
103147466731474668AT15GENIChomozygous116546600
103148602631486027TC11GENIChomozygous116546602
103148609031486091GA11GENIChomozygous116546604
103148680531486806TG11GENIChomozygous116752477
103148711931487120CT12GENIChomozygous116546606
103148760031487601GA11GENIChomozygous116546608
103148773131487732CT19GENIChomozygous116546610
103148853331488534AG13GENIChomozygous116546612
103148869031488691GA14GENIChomozygous116546614
103148871831488719GT12GENIChomozygous116546616
103148896331488964CG16GENIChomozygous116546618
103148904731489048GA15GENIChomozygous116546620
103148916731489168AG14GENIChomozygous116546622
103148966131489662CT16GENIChomozygous116546624
103149012931490130AG7GENIChomozygous116546626
103149122131491222TG9GENIChomozygous116546628
103149123531491236CT10GENIChomozygous116546630
103149166331491664GA7GENIChomozygous116752479
103149214431492145GA8GENIChomozygous116546632
103149254731492548TC16GENIChomozygous116546634
103149290531492906CT14GENIChomozygous116546636
103149305531493056AG12GENIChomozygous116546638
103149313331493134GA11GENIChomozygous116546640