chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149261085149261086CT74GENICpossibly homozygous112880972
4149261145149261146CT63GENIChomozygous112880974
4149261207149261208TG53GENIChomozygous112880976
4149261290149261291GC69GENIChomozygous112880978
4149261302149261303GC70GENIChomozygous112880980
4149261570149261570C74GENIChomozygous128090130
4149262475149262476GT48GENIChomozygous112880982
4149262734149262735TG53GENIChomozygous112880983
4149263191149263192AG41GENIChomozygous112880985
4149263832149263833CG30GENIChomozygous112880986
4149264140149264141TC39GENIChomozygous112880988
4149266163149266163A48GENIChomozygous128090131
4149266190149266191CG53GENIChomozygous112880990
4149266735149266736AT53GENIChomozygous112880992
4149267410149267411A40GENIChomozygous128090132
4149267751149267752AG52GENIChomozygous112880993
4149268403149268404AG34GENIChomozygous112880995
4149268735149268736GA51GENIChomozygous112880997
4149268750149268751GC54GENIChomozygous112880999
4149269079149269080GC54GENIChomozygous112881001
4149269399149269400GA56GENIChomozygous112881003
4149269416149269417CT61GENIChomozygous112881005
4149269863149269864GA48GENIChomozygous112881007
4149269917149269918A37GENIChomozygous128090133
4149270013149270014TC35GENIChomozygous112881009
4149270246149270247AG55GENIChomozygous112881011
4149270298149270299TG63GENIChomozygous112881013
4149270389149270390CT57GENIChomozygous112881015
4149272089149272090AG45GENIChomozygous112881017
4149272209149272210AG49GENIChomozygous112881019
4149272287149272288CT41GENIChomozygous112881020
4149272346149272347CG46GENIChomozygous112881022
4149273082149273083GT64GENIChomozygous112881024
4149273177149273178CT58GENIChomozygous112881025
4149273178149273179CT57GENIChomozygous112881027
4149273247149273248GA65GENIChomozygous112881028