chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,65195207,65195208,A,-,1,GENIC,homozygous,742807032 X,65195556,65195557,T,-,1,GENIC,homozygous,742807033 X,65208126,65208130,AGAG,----,1,GENIC,homozygous,742807035 X,65221013,65221014,T,G,7,GENIC,homozygous,619105526 X,65242215,65242216,C,G,6,GENIC,heterozygous,619105527 X,65244764,65244766,GT,--,3,GENIC,heterozygous,742807038 X,65252953,65252955,GT,--,8,GENIC,heterozygous,742807039 X,65257240,65257241,C,CT,7,GENIC,homozygous,742807040 X,65257397,65257398,C,CCTATGTACTGCACTTATCTACAATTTAGT,9,GENIC,homozygous,742807041 X,65259250,65259251,C,CGT,5,GENIC,heterozygous,742807042 X,65265754,65265756,TC,--,3,GENIC,heterozygous,742807043 X,65269452,65269453,C,-,9,GENIC,homozygous,742807044 X,65274821,65274822,G,-,17,GENIC,homozygous,742807045 X,65274840,65274841,G,-,21,GENIC,homozygous,742807046 X,65274846,65274847,C,T,21,GENIC,homozygous,619105528 X,65294793,65294794,A,-,4,GENIC,heterozygous,742807047 X,65295943,65295944,A,-,7,GENIC,heterozygous,742807048