chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4123706579123706580TC25GENIChomozygous113156038
4123709103123709104TC25GENIChomozygous113156040
4123713757123713758GA23GENIChomozygous113156043
4123715955123715956GT29GENIChomozygous113156044
4123717580123717581AT26GENIChomozygous113156046
4123718309123718310TC19GENIChomozygous113156047
4123719507123719508GA29GENIChomozygous113156048
4123722552123722553CT28GENIChomozygous113156049
4123722927123722928AG17GENIChomozygous113156050
4123723482123723483TC29GENIChomozygous113156051
4123725061123725062AG27GENIChomozygous113156052
4123725352123725353GC27GENIChomozygous113156053
4123725731123725732AG19GENIChomozygous113156054
4123725926123725927CG20GENIChomozygous113156055
4123727924123727925GA24GENIChomozygous113156058
4123728872123728873TA27GENIChomozygous113156059
4123729364123729365TA53GENIChomozygous113156060
4123732137123732138GA26GENIChomozygous113156062
4123732214123732215CT28GENIChomozygous113156063
4123732964123732965GA32GENIChomozygous113156064
4123733151123733152TG30GENIChomozygous113156065
4123733165123733166AG25GENIChomozygous113156066
4123733523123733524TG18GENIChomozygous113156067
4123737592123737593TC17GENIChomozygous113156069
4123737635123737636CT17GENIChomozygous113156070
4123737732123737733GA21GENIChomozygous113156071