chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,200037846,200037847,C,G,25,GENIC,homozygous,971696209 1,200089184,200089185,G,T,29,GENIC,homozygous,971696210 1,200089615,200089616,G,A,19,GENIC,homozygous,971696211 1,200091092,200091093,C,T,21,GENIC,homozygous,971696212 1,200092336,200092337,T,C,14,GENIC,homozygous,971696213 1,200096126,200096127,A,G,15,GENIC,homozygous,971696214 1,200096203,200096204,C,A,14,GENIC,homozygous,971696215 1,200096223,200096224,A,C,15,GENIC,homozygous,971696216 1,200099876,200099877,T,C,14,GENIC,homozygous,971696217 1,200101883,200101884,T,A,22,GENIC,homozygous,971696218 1,200101884,200101885,T,A,22,GENIC,homozygous,971696219 1,200102768,200102769,A,G,16,GENIC,homozygous,971696220 1,200103259,200103260,A,G,27,GENIC,homozygous,971696221 1,200103287,200103288,A,G,25,GENIC,homozygous,971696222 1,200103734,200103735,C,A,26,GENIC,homozygous,971696223 1,200103867,200103868,T,G,22,GENIC,homozygous,971696224 1,200103883,200103884,G,A,22,GENIC,homozygous,971696225 1,200105292,200105293,G,A,27,GENIC,homozygous,971696226 1,200107695,200107696,T,C,32,GENIC,homozygous,971696227 1,200111928,200111929,T,C,25,GENIC,homozygous,971696228 1,200112449,200112450,A,G,35,GENIC,homozygous,971696229 1,200112480,200112481,A,G,38,GENIC,homozygous,971696230 1,200112530,200112531,T,G,29,GENIC,homozygous,971696231 1,200112829,200112830,A,G,32,GENIC,homozygous,971696232 1,200115478,200115479,T,C,20,GENIC,homozygous,971696233