chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104651515746515158TC43GENIChomozygous116586180
104651550146515502CA30GENIChomozygous116772756
104652163146521632GA36GENIChomozygous116586184
104652321746523218TC11GENIChomozygous117008774
104652445946524460CT44GENIChomozygous116586186
104652643246526433GA30GENIChomozygous116772758
104653048546530486AG34GENIChomozygous116586188
104653571446535715TC33GENIChomozygous116586192
104653614246536143TC22GENIChomozygous116772764
104653683346536834GT31GENIChomozygous116877757
104652972246529723TG22GENIChomozygous116877751
104653276346532764GA35GENIChomozygous116877753
104653692446536925AT30GENIChomozygous116586194
104653718146537182TC29GENIChomozygous116586198
104653765846537659TC38GENIChomozygous116877759
104653798446537985TC20GENIChomozygous116586200
104653901446539015GA39GENIChomozygous116877761
104654140046541401AG30GENIChomozygous116586202
104654265446542655CT32GENIChomozygous116877763
104654600246546003GA35GENIChomozygous116877765
104654608746546088GA41GENIChomozygous116877768
104655157346551574GC33GENIChomozygous116586212
104655198646551987CT38GENIChomozygous116877770
104655390446553905TC28GENIChomozygous116877772
104655551046555511GA31GENIChomozygous116877774
104655574846555749GA35GENIChomozygous116877776
104656246046562461AG32GENIChomozygous116877778
104656317546563176CT20GENIChomozygous116877780
104656362346563624CA32GENIChomozygous116877785
104656368846563689GA22GENIChomozygous116877787
104656386046563861GA26GENIChomozygous116877789
104656504846565049GT25GENIChomozygous116877791
104656506746565068CT28GENIChomozygous116877793
104656520946565210TC24GENIChomozygous116877795
104656561246565613GT29GENIChomozygous116586222
104656663446566635GA26GENIChomozygous116877797
104657129946571300GA37GENIChomozygous116877803