chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25853789958537900AG45GENIChomozygous109772548
25853903058539031AG24GENIChomozygous109772550
25854094158540942TC10GENIChomozygous109772557
25854098358540984AG16GENIChomozygous109772559
25854448458544485TC11GENIChomozygous109772563
25854743158547432CT30GENIChomozygous109772585
25855371358553714TC22GENIChomozygous109772589
25855393758553938CT31GENIChomozygous109772591
25855409358554094GA45GENIChomozygous109772593
25855454858554549TC21GENIChomozygous109772595
25855461658554617TC21GENIChomozygous109772597
25855493058554931AG33GENIChomozygous109772599
25855518358555184GA11GENIChomozygous109772601
25855520758555208AT2GENIChomozygous109772603
25855608258556083TA14GENIChomozygous109772605
25855780858557809CT52GENIChomozygous109772607
25856210558562106GA21GENICpossibly homozygous109772609
25856254558562546CT27GENIChomozygous109772611
25856449458564495GA39GENIChomozygous109772613
25856470958564710AG30GENIChomozygous109772615
25856784058567841AG49GENIChomozygous109772625
25856785458567855GA40GENIChomozygous109772627
25857062258570623GA19GENIChomozygous109772629
25857091258570913TG30GENIChomozygous109772631
25857091358570914TG30GENIChomozygous109772633
25857091458570915TC31GENIChomozygous109772635
25857532258575323TC23GENIChomozygous109772637
25857792658577927GA19GENIChomozygous109772641
25857802958578030AG26GENIChomozygous109772643
25858167358581674AT20GENIChomozygous109772645
25858239758582398TC17GENIChomozygous120143592
25858316758583168GA18GENIChomozygous109772647
25858423358584234GA15GENIChomozygous109772649
25858497558584976CT21GENIChomozygous109772650
25858756158587562GA29GENIChomozygous109772656
25858774458587745GC40GENIChomozygous109772658
25858796158587962AT11GENIChomozygous109772660
25858803158588032TC16GENIChomozygous109772662
25858818858588189TC28GENIChomozygous109772664
25858856658588567AC24GENIChomozygous109772666
25858893458588935TC17GENIChomozygous109772668