chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104651515746515158TC32GENIChomozygous116586180
104651550146515502CA20GENIChomozygous116772756
104652163146521632GA35GENIChomozygous116586184
104652445946524460CT35GENIChomozygous116586186
104652643246526433GA30GENIChomozygous116772758
104653048546530486AG22GENIChomozygous116586188
104653571446535715TC27GENIChomozygous116586192
104653614246536143TC25GENIChomozygous116772764
104653692446536925AT24GENIChomozygous116586194
104653718146537182TC26GENIChomozygous116586198
104653798446537985TC24GENIChomozygous116586200
104654140046541401AG18GENIChomozygous116586202
104654179046541791TC44GENIChomozygous116586204
104654600246546003GA27GENIChomozygous116877765
104652972246529723TG19GENIChomozygous116877751
104653276346532764GA28GENIChomozygous116877753
104653683346536834GT23GENIChomozygous116877757
104653765846537659TC29GENIChomozygous116877759
104653901446539015GA25GENICpossibly homozygous116877761
104654265446542655CT24GENIChomozygous116877763
104654608746546088GA23GENIChomozygous116877768
104655073346550734TC25GENIChomozygous116586210
104655157346551574GC21GENIChomozygous116586212
104655198646551987CT23GENIChomozygous116877770
104655390446553905TC43GENIChomozygous116877772
104655551046555511GA29GENIChomozygous116877774
104655574846555749GA38GENIChomozygous116877776
104656156446561565TC20GENIChomozygous116586218
104656246046562461AG27GENIChomozygous116877778
104656317546563176CT16GENIChomozygous116877780
104656359646563597AT24GENIChomozygous116877783
104656362346563624CA33GENIChomozygous116877785
104656386046563861GA26GENIChomozygous116877789
104656504846565049GT33GENIChomozygous116877791
104656506746565068CT36GENIChomozygous116877793
104656520946565210TC17GENIChomozygous116877795
104656561246565613GT38GENIChomozygous116586222
104656663446566635GA26GENIChomozygous116877797
104657069046570691GA25GENIChomozygous116877801
104657129946571300GA22GENIChomozygous116877803