chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
156072235060722351AG32GENIChomozygous953429037
156072251560722516CT17GENIChomozygous953429038
156072300660723007TG13GENIChomozygous953429039
156072320060723201AC26GENIChomozygous953429040
156072339460723395TA38GENIChomozygous953429041
156072358960723590CT20GENIChomozygous953429042
156072404160724042TG37GENIChomozygous953429043
156072404360724044TC37GENIChomozygous953429044
156072406660724067AG34GENIChomozygous953429045
156072410360724104TC26GENIChomozygous953429046
156072418360724184TC29GENIChomozygous953429047
156072557560725576TC28GENIChomozygous953429048
156072762960727630CT21GENIChomozygous953429049
156072763060727631CA22GENIChomozygous953429050
156073477660734777TA20GENIChomozygous953429051
156073854060738541GA24GENIChomozygous953429052
156073873060738731CT32GENIChomozygous953429053
156073893760738938GA34GENIChomozygous953429054
156073906260739063GA19GENIChomozygous953429055
156074183860741839CT35GENIChomozygous953429056
156074745360747454AG29GENIChomozygous953429057
156074838960748390CA16GENICheterozygous953429058
156074907160749072GT24GENIChomozygous953429059
156074908060749081GA25GENIChomozygous953429060
156074995560749956CA26GENIChomozygous953429061
156075067960750680AG24GENIChomozygous953429062
156075134560751346TC33GENIChomozygous953429063
156075184260751843TA25GENIChomozygous953429064
156075431260754313TC21GENIChomozygous953429065
156075599360755994AG30GENIChomozygous953429066
156076161960761620TG20GENIChomozygous953429067
156076164660761647GA17GENIChomozygous953429068
156076218560762186GA25GENIChomozygous953429069
156076598760765988AG24GENIChomozygous953429070
156076648860766489GC7GENIChomozygous953429071
156076649160766492AC10GENIChomozygous953429072