chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,110901804,110901805,G,A,14,GENIC,homozygous,887112189 X,110904072,110904073,G,T,9,GENIC,heterozygous,887112190 X,110906891,110906892,C,T,7,GENIC,homozygous,887112191 X,110906892,110906893,C,T,7,GENIC,homozygous,887112192 X,110911116,110911117,C,A,7,GENIC,homozygous,887112193 X,110915401,110915402,C,T,4,GENIC,homozygous,887112194 X,110917889,110917890,A,G,7,GENIC,heterozygous,887112195 X,110917920,110917921,C,A,4,GENIC,heterozygous,887112196 X,110922014,110922015,C,G,4,GENIC,homozygous,887112197 X,110944090,110944091,C,A,8,GENIC,homozygous,887112198 X,110944322,110944323,A,G,4,GENIC,homozygous,887112199 X,110944345,110944346,A,G,5,GENIC,homozygous,887112200 X,110969698,110969699,C,A,12,GENIC,homozygous,887112202 X,110975092,110975093,G,C,7,GENIC,heterozygous,886208595