chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103145369931453700GT24GENIChomozygous116546580
103145371131453712AG24GENIChomozygous116546582
103145372231453723AG23GENIChomozygous116546584
103145373731453738AG23GENIChomozygous116546586
103146206031462061TC21GENIChomozygous116546588
103146501431465015GT27GENIChomozygous116546590
103146504831465049CG20GENIChomozygous116546592
103146505031465051GT20GENIChomozygous116546594
103146540031465401AC20GENIChomozygous116546596
103147466731474668AT23GENIChomozygous116546600
103148602631486027TC30GENIChomozygous116546602
103148609031486091GA24GENIChomozygous116546604
103148680531486806TG25GENIChomozygous116752477
103148711931487120CT28GENIChomozygous116546606
103148760031487601GA30GENIChomozygous116546608
103148773131487732CT32GENIChomozygous116546610
103148853331488534AG28GENIChomozygous116546612
103148869031488691GA27GENIChomozygous116546614
103148871831488719GT22GENIChomozygous116546616
103148896331488964CG28GENIChomozygous116546618
103148904731489048GA25GENIChomozygous116546620
103148916731489168AG20GENIChomozygous116546622
103148966131489662CT29GENIChomozygous116546624
103149012931490130AG22GENIChomozygous116546626
103149122131491222TG21GENIChomozygous116546628
103149123531491236CT24GENIChomozygous116546630
103149166331491664GA30GENIChomozygous116752479
103149214431492145GA38GENIChomozygous116546632
103149254731492548TC20GENIChomozygous116546634
103149290531492906CT33GENIChomozygous116546636
103149305531493056AG17GENIChomozygous116546638
103149313331493134GA24GENIChomozygous116546640