chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149261085149261086CT23GENIChomozygous112880972
4149261145149261146CT24GENIChomozygous112880974
4149261207149261208TG25GENIChomozygous112880976
4149261290149261291GC30GENIChomozygous112880978
4149261302149261303GC29GENIChomozygous112880980
4149261570149261570C29GENIChomozygous128090130
4149262474149262475G17GENICheterozygous131363450
4149262475149262476GT17GENICheterozygous112880982
4149262734149262735TG25GENIChomozygous112880983
4149263191149263192AG19GENIChomozygous112880985
4149263832149263833CG28GENIChomozygous112880986
4149266163149266163A19GENIChomozygous128090131
4149267410149267411A26GENIChomozygous128090132
4149268403149268404AG26GENIChomozygous112880995
4149264140149264141TC26GENIChomozygous112880988
4149266190149266191CG17GENIChomozygous112880990
4149266735149266736AT35GENIChomozygous112880992
4149267751149267752AG27GENIChomozygous112880993
4149268735149268736GA26GENIChomozygous112880997
4149268750149268751GC26GENIChomozygous112880999
4149269079149269080GC30GENIChomozygous112881001
4149269399149269400GA25GENIChomozygous112881003
4149269416149269417CT25GENIChomozygous112881005
4149269863149269864GA16GENIChomozygous112881007
4149269917149269918A17GENIChomozygous128090133
4149270013149270014TC22GENIChomozygous112881009
4149270246149270247AG19GENIChomozygous112881011
4149270298149270299TG28GENIChomozygous112881013
4149270389149270390CT32GENIChomozygous112881015
4149272089149272090AG32GENIChomozygous112881017
4149272209149272210AG31GENIChomozygous112881019
4149272287149272288CT35GENIChomozygous112881020
4149272346149272347CG36GENIChomozygous112881022
4149273082149273083GT22GENICpossibly homozygous112881024
4149273177149273178CT26GENIChomozygous112881025
4149273178149273179CT26GENIChomozygous112881027
4149273247149273248GA26GENIChomozygous112881028