chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
177728787977287880AG16GENIChomozygous111099568
177728949577289496GA26GENIChomozygous111099570
177728950977289510TC26GENIChomozygous111099572
177729020077290201TC18GENIChomozygous111099574
177729094377290944TC11GENIChomozygous111099576
177729104977291050CT24GENIChomozygous111099578
177729132577291326CT34GENIChomozygous111099580
177729169077291691TC36GENIChomozygous111099584
177729174177291742TC31GENIChomozygous111099586
177729192677291927GA19GENIChomozygous111099588
177729218777292188TC19GENIChomozygous111099590
177729224277292243GC14GENIChomozygous111099592
177729272177292722GA25GENIChomozygous111099594
177729309077293091GA30GENIChomozygous111099596
177729312077293121CG23GENIChomozygous111099598
177729356077293561AG20GENIChomozygous111099600
177729421477294215CT22GENIChomozygous111099602
177729475477294755AG29GENIChomozygous111099604
177729497077294971CT26GENIChomozygous111311259
177729668777296688CT35GENIChomozygous111099606
177729805477298055CA20GENIChomozygous111099608
177729829977298300TC29GENIChomozygous111099610
177729838277298383TC34GENIChomozygous111099612
177730135477301355GA24GENIChomozygous111099614
177730152877301529GA24GENIChomozygous111099616
177730317477303175TC12GENIChomozygous111099618
177730319977303200GA15GENIChomozygous111099620
177730366977303670TC22GENIChomozygous111099622
177730378977303790AC33GENIChomozygous111099624
177730393777303938GA31GENIChomozygous111099626
177730416177304162GT22GENIChomozygous111099628
177730427577304276CT23GENIChomozygous111099630
177730430077304301GT22GENIChomozygous111099632
177730146877301469GA30GENIChomozygous111213798
177730123077301231TA37GENIChomozygous111213796
177730141577301416TC27GENIChomozygous111213797