chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8132828942132828943GA18GENIChomozygous116905484
8132829194132829195CT23GENIChomozygous116905486
8132831177132831178GA21GENIChomozygous116905488
8132832819132832820TC15GENIChomozygous116730002
8132834594132834595AG16GENIChomozygous116905490
8132835630132835631TC16GENIChomozygous116730009
8132835847132835848CG17GENIChomozygous116905492
8132835992132835993AG17GENIChomozygous116905494
8132836100132836101AG28GENIChomozygous116905496
8132836252132836253GT24GENIChomozygous116730010
8132836459132836460GA24GENIChomozygous116905498
8132836539132836540GA13GENIChomozygous116905500
8132836550132836551CA14GENIChomozygous116905502
8132836608132836609AG14GENIChomozygous116905504
8132836902132836903TG28GENIChomozygous116905506
8132837174132837175AC24GENIChomozygous116905508
8132837196132837197TC19GENIChomozygous116905510
8132838025132838026GT22GENIChomozygous116905512
8132838253132838254GA22GENICpossibly homozygous116905514
8132838389132838390GA31GENIChomozygous116905516
8132838490132838491TC28GENICpossibly homozygous116905518
8132838681132838682AT26GENIChomozygous116905520
8132839257132839258CT18GENIChomozygous116905522
8132839373132839374TG27GENIChomozygous116730011
8132839601132839602TC20GENIChomozygous116905524
8132840641132840642TC15GENIChomozygous116905526