chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8132828839132828848ATATATATA5GENIChomozygous131056250
8132828942132828943GA13GENIChomozygous116905484
8132829194132829195CT13GENIChomozygous116905486
8132831177132831178GA13GENIChomozygous116905488
8132832819132832820TC23GENIChomozygous116730002
8132833593132833594T14GENIChomozygous128651127
8132834594132834595AG13GENIChomozygous116905490
8132835630132835631TC13GENIChomozygous116730009
8132835811132835811T14GENIChomozygous131056251
8132836459132836460GA13GENIChomozygous116905498
8132835847132835848CG14GENIChomozygous116905492
8132835992132835993AG9GENIChomozygous116905494
8132836100132836101AG14GENIChomozygous116905496
8132836252132836253GT12GENIChomozygous116730010
8132836539132836540GA11GENIChomozygous116905500
8132836550132836551CA13GENIChomozygous116905502
8132836608132836609AG16GENIChomozygous116905504
8132836902132836903TG18GENIChomozygous116905506
8132837174132837175AC18GENIChomozygous116905508
8132837196132837197TC15GENIChomozygous116905510
8132837555132837555TTAAGTAG21GENIChomozygous131056252
8132837750132837750T15GENIChomozygous131056253
8132838025132838026GT25GENICpossibly homozygous116905512
8132838253132838254GA27GENIChomozygous116905514
8132838389132838390GA28GENIChomozygous116905516
8132838490132838491TC25GENIChomozygous116905518
8132838681132838682AT20GENIChomozygous116905520
8132839202132839202ACTT21GENIChomozygous131056254
8132839257132839258CT24GENIChomozygous116905522
8132839373132839374TG14GENIChomozygous116730011
8132839601132839602TC21GENIChomozygous116905524
8132840641132840642TC17GENIChomozygous116905526