chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 18,59409424,59409425,G,C,26,GENIC,homozygous,971282340 18,59409466,59409467,C,T,26,GENIC,homozygous,971282341 18,59409470,59409471,C,T,29,GENIC,homozygous,971282342 18,59409713,59409714,A,G,18,GENIC,homozygous,971282343 18,59409716,59409717,C,T,20,GENIC,homozygous,971282344 18,59410596,59410597,C,A,31,GENIC,homozygous,971282345 18,59410868,59410869,G,A,17,GENIC,homozygous,971282346 18,59410952,59410953,T,C,35,GENIC,homozygous,971282347 18,59411050,59411051,A,G,33,GENIC,homozygous,971282348 18,59411085,59411086,A,G,29,GENIC,homozygous,971282349 18,59411508,59411509,C,T,31,GENIC,homozygous,971282350 18,59412955,59412956,C,T,32,GENIC,homozygous,971282351 18,59413457,59413458,T,A,35,GENIC,homozygous,971282352 18,59414673,59414674,T,C,31,GENIC,homozygous,971282353 18,59416433,59416434,G,A,8,GENIC,homozygous,971282354 18,59417487,59417488,C,T,21,GENIC,homozygous,971282355 18,59417833,59417834,T,C,37,GENIC,homozygous,971282356 18,59417943,59417944,T,A,29,GENIC,homozygous,971282357