chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8132828942132828943GA19GENIChomozygous116905484
8132829194132829195CT28GENIChomozygous116905486
8132831177132831178GA15GENIChomozygous116905488
8132832819132832820TC22GENIChomozygous116730002
8132834594132834595AG13GENIChomozygous116905490
8132835630132835631TC18GENIChomozygous116730009
8132835811132835811T15GENIChomozygous131056251
8132835847132835848CG14GENIChomozygous116905492
8132835992132835993AG34GENIChomozygous116905494
8132836100132836101AG24GENIChomozygous116905496
8132836252132836253GT19GENIChomozygous116730010
8132836459132836460GA31GENIChomozygous116905498
8132836539132836540GA22GENIChomozygous116905500
8132836550132836551CA23GENIChomozygous116905502
8132836608132836609AG21GENIChomozygous116905504
8132836902132836903TG24GENIChomozygous116905506
8132837174132837175AC21GENIChomozygous116905508
8132837196132837197TC23GENIChomozygous116905510
8132837555132837555TTAAGTAG16GENIChomozygous131056252
8132837750132837750T17GENIChomozygous131056253
8132838389132838390GA29GENIChomozygous116905516
8132833593132833594T24GENIChomozygous128651127
8132835100132835101CT27GENIChomozygous117150408
8132838025132838026GT18GENIChomozygous116905512
8132838253132838254GA19GENIChomozygous116905514
8132838490132838491TC22GENIChomozygous116905518
8132838681132838682AT20GENIChomozygous116905520
8132839202132839202ACTT21GENIChomozygous131056254
8132839257132839258CT23GENIChomozygous116905522
8132839373132839374TG27GENIChomozygous116730011
8132839601132839602TC20GENIChomozygous116905524
8132840641132840642TC23GENIChomozygous116905526