chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4123706579123706580TC18GENIChomozygous113156038
4123708656123708657CT13GENIChomozygous113156039
4123709103123709104TC19GENIChomozygous113156040
4123710195123710196AT23GENIChomozygous113156041
4123713099123713100CT6GENIChomozygous113156042
4123713757123713758GA21GENIChomozygous113156043
4123715955123715956GT18GENIChomozygous113156044
4123716739123716740TC24GENIChomozygous113156045
4123717580123717581AT21GENIChomozygous113156046
4123718309123718310TC15GENIChomozygous113156047
4123719507123719508GA26GENIChomozygous113156048
4123722552123722553CT27GENIChomozygous113156049
4123722927123722928AG17GENIChomozygous113156050
4123723482123723483TC25GENIChomozygous113156051
4123725061123725062AG14GENIChomozygous113156052
4123725352123725353GC19GENIChomozygous113156053
4123725731123725732AG23GENIChomozygous113156054
4123725926123725927CG29GENIChomozygous113156055
4123727383123727384AG18GENICheterozygous113156056
4123727391123727392AG17GENICheterozygous113156057
4123727924123727925GA21GENICpossibly homozygous113156058
4123728872123728873TA19GENIChomozygous113156059
4123729364123729365TA37GENIChomozygous113156060
4123729407123729408AG34GENIChomozygous113156061
4123732137123732138GA21GENIChomozygous113156062
4123732214123732215CT9GENIChomozygous113156063
4123732964123732965GA21GENIChomozygous113156064
4123733151123733152TG21GENIChomozygous113156065
4123733165123733166AG21GENIChomozygous113156066
4123733523123733524TG27GENIChomozygous113156067
4123733599123733600CA14GENIChomozygous113156068
4123737592123737593TC21GENIChomozygous113156069
4123737635123737636CT19GENIChomozygous113156070
4123737732123737733GA24GENIChomozygous113156071