chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149261085149261086CT27GENIChomozygous112880972
4149261145149261146CT25GENIChomozygous112880974
4149261207149261208TG29GENIChomozygous112880976
4149261290149261291GC22GENIChomozygous112880978
4149261302149261303GC21GENIChomozygous112880980
4149262475149262476GT22GENIChomozygous112880982
4149262734149262735TG26GENIChomozygous112880983
4149263191149263192AG21GENIChomozygous112880985
4149263832149263833CG26GENIChomozygous112880986
4149264140149264141TC15GENIChomozygous112880988
4149266190149266191CG39GENIChomozygous112880990
4149266735149266736AT33GENIChomozygous112880992
4149267751149267752AG17GENIChomozygous112880993
4149268403149268404AG32GENIChomozygous112880995
4149268735149268736GA20GENIChomozygous112880997
4149268750149268751GC23GENIChomozygous112880999
4149269079149269080GC27GENIChomozygous112881001
4149269399149269400GA29GENIChomozygous112881003
4149269416149269417CT26GENIChomozygous112881005
4149269863149269864GA20GENIChomozygous112881007
4149270246149270247AG17GENIChomozygous112881011
4149270298149270299TG25GENIChomozygous112881013
4149270389149270390CT23GENIChomozygous112881015
4149272089149272090AG35GENIChomozygous112881017
4149272209149272210AG33GENIChomozygous112881019
4149272287149272288CT34GENIChomozygous112881020
4149272346149272347CG30GENIChomozygous112881022
4149273082149273083GT16GENIChomozygous112881024
4149273177149273178CT25GENIChomozygous112881025
4149273178149273179CT26GENIChomozygous112881027
4149273247149273248GA41GENIChomozygous112881028