chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147190016771900168CG36GENICpossibly homozygous113488704
147190025371900254CA46GENIChomozygous113488705
147190027771900278CG52GENIChomozygous113488706
147190027971900280CA53GENIChomozygous113488707
147190030571900306CA52GENIChomozygous113488708
147190031271900313CA54GENICpossibly homozygous113488709
147192658571926586CT9GENIChomozygous113488710
147192699371926994AC16GENIChomozygous113488711
147194373771943738AG42GENICheterozygous118702017
147194382571943826TC55GENICheterozygous118805662
147194426371944264AG248GENICheterozygous118702019
147194432171944322AG142GENICheterozygous118702020
147194434571944346CT96GENICheterozygous118702021
147194519671945197GA177GENICheterozygous118805663
147194627671946277GC118GENICheterozygous118805665
147194628271946283CA123GENICheterozygous118805666
147194637771946378TC193GENICheterozygous118702026
147194640171946402AG209GENICheterozygous118702027
147194643671946437CA198GENICheterozygous118702028
147194644971946450AT183GENICheterozygous118702029
147194647271946473CA182GENICheterozygous118764800
147194647871946479TA184GENICheterozygous118764801
147194713171947132AG88GENICheterozygous118805668
147194718171947182TC122GENICheterozygous118805669
147194718271947183AT121GENICheterozygous118702030
147194719771947198AC121GENICheterozygous118702031