chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149261085149261086CT39GENIChomozygous112880972
4149261145149261146CT38GENIChomozygous112880974
4149261207149261208TG33GENIChomozygous112880976
4149261290149261291GC37GENIChomozygous112880978
4149261302149261303GC46GENIChomozygous112880980
4149262734149262735TG42GENIChomozygous112880983
4149263191149263192AG37GENIChomozygous112880985
4149263832149263833CG40GENIChomozygous112880986
4149264140149264141TC39GENIChomozygous112880988
4149266190149266191CG35GENIChomozygous112880990
4149266735149266736AT42GENIChomozygous112880992
4149267751149267752AG27GENIChomozygous112880993
4149268403149268404AG40GENIChomozygous112880995
4149268735149268736GA50GENIChomozygous112880997
4149268750149268751GC46GENIChomozygous112880999
4149269079149269080GC30GENIChomozygous112881001
4149269399149269400GA50GENIChomozygous112881003
4149269416149269417CT54GENIChomozygous112881005
4149269863149269864GA18GENIChomozygous112881007
4149270246149270247AG40GENIChomozygous112881011
4149270298149270299TG36GENIChomozygous112881013
4149270389149270390CT34GENIChomozygous112881015
4149272089149272090AG48GENIChomozygous112881017
4149272209149272210AG55GENIChomozygous112881019
4149272287149272288CT34GENIChomozygous112881020
4149272346149272347CG35GENIChomozygous112881022
4149273082149273083GT31GENIChomozygous112881024
4149273177149273178CT49GENIChomozygous112881025
4149273178149273179CT50GENIChomozygous112881027
4149273247149273248GA40GENIChomozygous112881028