chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28453593184535932TG23GENIChomozygous109886660
28453746884537469GA28GENIChomozygous110946029
28453771884537719TC33GENIChomozygous110946031
28453859184538592CT26GENIChomozygous110946033
28453979184539792CT9GENIChomozygous109886667
28453979284539793AT9GENIChomozygous120198914
28453980784539808GA9GENIChomozygous110946035
28454064284540643CT31GENIChomozygous109886669
28454140684541407GA18GENICpossibly homozygous120198915
28454269384542694CA7GENIChomozygous120198916
28455069484550695TC23GENIChomozygous110946043
28455070884550709CT24GENIChomozygous110946045
28455160584551606AC24GENIChomozygous109886685
28455203584552036AC39GENIChomozygous109886687
28455238784552388CG20GENIChomozygous109886690
28455695584556956GA19GENIChomozygous110946060
28456103384561034AT28GENIChomozygous109886711
28456121984561220TA30GENIChomozygous109886713
28456124184561242GA26GENIChomozygous110946066
28456127384561274CT28GENIChomozygous109886715
28456279684562797AG23GENIChomozygous109886718
28456331184563312AT30GENIChomozygous109886720
28456553384565534GA25GENIChomozygous120391237
28456882084568821AG22GENIChomozygous109886722
28457019684570197CT23GENIChomozygous110946072
28457182984571830CT41GENIChomozygous120198917
28457350684573507AG20GENIChomozygous109886733
28457559384575594TA29GENIChomozygous109886736
28457605184576052CT33GENIChomozygous109886738
28457711984577120GA25GENIChomozygous109886740
28458145484581455CA21GENIChomozygous109886742
28458472984584730AG26GENIChomozygous110946080
28458525884585259GC26GENIChomozygous109886747
28458596384585964GA33GENICpossibly homozygous120198918
28458827884588279CT28GENIChomozygous109886759
28459004784590048GA27GENIChomozygous120198919
28459939584599396CT32GENIChomozygous120198920
28460171584601716AG35GENIChomozygous109886770
28460325484603255GA16GENIChomozygous109886773