chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,110903046,110903047,A,T,6,GENIC,homozygous,959814697 X,110903049,110903050,T,A,6,GENIC,homozygous,959814698 X,110903511,110903512,G,C,12,GENIC,homozygous,959814699 X,110906891,110906892,C,T,12,GENIC,homozygous,959814700 X,110906892,110906893,C,T,12,GENIC,homozygous,959814701 X,110911116,110911117,C,A,5,GENIC,homozygous,959814702 X,110940136,110940137,G,T,14,GENIC,homozygous,959814703 X,110940211,110940212,G,A,12,GENIC,homozygous,959814704 X,110957382,110957383,T,A,4,GENIC,homozygous,959814705 X,110957386,110957387,A,T,4,GENIC,homozygous,959814706