chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5136795287136795288AG19GENIChomozygous186418432
5136796362136796363TC12GENIChomozygous186418433
5136797942136797943CG15GENIChomozygous185631835
5136797958136797959TA8GENICheterozygous186418434
5136798035136798036AG11GENIChomozygous185631836
5136798053136798054TC11GENIChomozygous185631837
5136799745136799746CT18GENIChomozygous185631838
5136801209136801210GT25GENIChomozygous186418435
5136801244136801245GA18GENIChomozygous186418436
5136802287136802288TA8GENIChomozygous186418437
5136805808136805809GA17GENIChomozygous186418438
5136806947136806948CT6GENIChomozygous185631839
5136808016136808017CT20GENIChomozygous186418439
5136808182136808183TC23GENICpossibly homozygous185631840
5136808582136808583GA22GENIChomozygous186418440
5136808907136808908CT17GENIChomozygous186418441
5136809888136809889CT19GENIChomozygous186418442
5136810310136810311TC6GENICheterozygous186418443
5136810694136810695CT16GENIChomozygous186418444
5136811151136811152TG4GENIChomozygous186418445
5136811157136811158CT4GENIChomozygous186418446
5136812070136812071CT9GENIChomozygous186418447
5136814019136814020CT9GENIChomozygous186418448
5136814331136814332TG17GENIChomozygous186418449
5136815930136815931TC9GENIChomozygous186418450
5136815996136815997TC10GENIChomozygous186418451
5136817356136817357CT7GENIChomozygous186418452
5136817505136817506GA8GENIChomozygous185631841
5136819351136819352GA11GENIChomozygous186418453
5136820023136820024TC7GENIChomozygous186418454
5136822954136822955TC14GENIChomozygous185631842
5136824273136824274CG28GENIChomozygous185631843
5136825028136825029TA13GENIChomozygous185631844