chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,105293208,105293209,A,G,12,GENIC,homozygous,981026312 X,105293287,105293288,A,T,11,GENIC,homozygous,981026313 X,105295440,105295441,G,A,9,GENIC,homozygous,981026314 X,105296887,105296888,T,A,4,GENIC,homozygous,981026315 X,105297118,105297119,C,T,7,GENIC,homozygous,981026316 X,105297905,105297906,T,A,9,GENIC,homozygous,981026317 X,105298659,105298660,A,C,7,GENIC,homozygous,981026318 X,105302163,105302164,C,A,16,GENIC,homozygous,981026319 X,105302184,105302185,T,C,15,GENIC,homozygous,981026320 X,105302210,105302211,C,A,10,GENIC,homozygous,981026321 X,105302256,105302257,G,C,6,GENIC,homozygous,981026322 X,105303025,105303026,T,G,8,GENIC,homozygous,981026323 X,105303915,105303916,A,G,13,GENIC,homozygous,981026324 X,105308529,105308530,A,G,27,GENIC,homozygous,981026325