chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,14530342,14530343,T,G,5,GENIC,homozygous,140616099 X,14531821,14531822,C,T,11,GENIC,homozygous,140616100 X,14532201,14532202,G,A,6,GENIC,homozygous,140616101 X,14532477,14532477,,A,3,GENIC,homozygous,145096460 X,14532609,14532610,T,C,3,GENIC,homozygous,140616102 X,14533450,14533451,C,G,8,GENIC,homozygous,140616103 X,14533697,14533698,T,C,11,GENIC,homozygous,140616104 X,14536236,14536237,C,T,12,GENIC,homozygous,140616105