chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149261085149261086CT26GENIChomozygous112880972
4149261145149261146CT27GENIChomozygous112880974
4149261207149261208TG26GENIChomozygous112880976
4149261290149261291GC27GENIChomozygous112880978
4149261302149261303GC27GENIChomozygous112880980
4149262475149262476GT35GENICpossibly homozygous112880982
4149262734149262735TG42GENIChomozygous112880983
4149263191149263192AG43GENIChomozygous112880985
4149263832149263833CG35GENIChomozygous112880986
4149264140149264141TC25GENIChomozygous112880988
4149266190149266191CG45GENIChomozygous112880990
4149266735149266736AT30GENIChomozygous112880992
4149267751149267752AG53GENIChomozygous112880993
4149268403149268404AG43GENIChomozygous112880995
4149268735149268736GA56GENIChomozygous112880997
4149268750149268751GC52GENIChomozygous112880999
4149269079149269080GC35GENIChomozygous112881001
4149269399149269400GA38GENIChomozygous112881003
4149269416149269417CT38GENIChomozygous112881005
4149269863149269864GA45GENIChomozygous112881007
4149270013149270014TC13GENIChomozygous112881009
4149270246149270247AG36GENIChomozygous112881011
4149270298149270299TG29GENIChomozygous112881013
4149270389149270390CT33GENIChomozygous112881015
4149272089149272090AG45GENIChomozygous112881017
4149272209149272210AG38GENIChomozygous112881019
4149272287149272288CT40GENIChomozygous112881020
4149272346149272347CG50GENIChomozygous112881022
4149273082149273083GT37GENIChomozygous112881024
4149273177149273178CT23GENIChomozygous112881025
4149273178149273179CT23GENIChomozygous112881027
4149273247149273248GA21GENIChomozygous112881028