chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,123900771,123900772,C,T,17,GENIC,homozygous,805627091 X,123901333,123901334,T,C,7,GENIC,homozygous,805627092 X,123901666,123901667,C,A,11,GENIC,homozygous,805627093 X,123903096,123903097,C,T,10,GENIC,homozygous,805627094 X,123905627,123905628,A,G,5,GENIC,homozygous,805627095 X,123906855,123906856,C,T,8,GENIC,homozygous,805627096 X,123907940,123907941,C,A,9,GENIC,heterozygous,805627097 X,123908451,123908452,C,T,8,GENIC,homozygous,805627098 X,123910070,123910071,T,G,10,GENIC,homozygous,805627099 X,123910082,123910083,A,G,9,GENIC,homozygous,805627100 X,123910759,123910760,A,C,10,GENIC,homozygous,805627101 X,123910765,123910766,T,G,10,GENIC,homozygous,805627102 X,123910914,123910915,T,A,15,GENIC,homozygous,805627103 X,123911193,123911194,A,T,4,GENIC,homozygous,805627104 X,123911321,123911322,T,C,14,GENIC,homozygous,805627105 X,123911461,123911462,G,T,17,GENIC,homozygous,805627106