chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149261085149261086CT52GENIChomozygous112880972
4149261145149261146CT59GENIChomozygous112880974
4149261207149261208TG47GENIChomozygous112880976
4149261290149261291GC30GENIChomozygous112880978
4149261302149261303GC25GENIChomozygous112880980
4149262475149262476GT16GENICpossibly homozygous112880982
4149262734149262735TG34GENIChomozygous112880983
4149263191149263192AG13GENIChomozygous112880985
4149263832149263833CG21GENIChomozygous112880986
4149264140149264141TC27GENIChomozygous112880988
4149266190149266191CG35GENIChomozygous112880990
4149266735149266736AT34GENIChomozygous112880992
4149267751149267752AG35GENIChomozygous112880993
4149268403149268404AG20GENIChomozygous112880995
4149268735149268736GA24GENIChomozygous112880997
4149268750149268751GC25GENIChomozygous112880999
4149269079149269080GC32GENIChomozygous112881001
4149269399149269400GA32GENIChomozygous112881003
4149269416149269417CT30GENIChomozygous112881005
4149269863149269864GA26GENIChomozygous112881007
4149270013149270014TC32GENIChomozygous112881009
4149270246149270247AG26GENIChomozygous112881011
4149270298149270299TG27GENIChomozygous112881013
4149270389149270390CT20GENIChomozygous112881015
4149272089149272090AG49GENIChomozygous112881017
4149272209149272210AG28GENIChomozygous112881019
4149272287149272288CT19GENIChomozygous112881020
4149272346149272347CG22GENIChomozygous112881022
4149273082149273083GT30GENIChomozygous112881024
4149273177149273178CT33GENIChomozygous112881025
4149273178149273179CT33GENIChomozygous112881027
4149273247149273248GA39GENIChomozygous112881028