chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,214127746,214127747,G,C,30,GENIC,homozygous,978017493 1,214128734,214128735,C,T,30,GENIC,homozygous,978017494 1,214128881,214128882,C,G,34,GENIC,homozygous,978017495 1,214130010,214130011,G,A,47,GENIC,homozygous,978017496 1,214131357,214131358,A,G,58,GENIC,homozygous,978017497 1,214132530,214132531,C,T,72,GENIC,homozygous,978017498 1,214132768,214132769,C,G,29,GENIC,homozygous,978017499 1,214135782,214135783,A,G,45,GENIC,homozygous,978017500 1,214136646,214136647,G,A,55,GENIC,homozygous,978017501 1,214138264,214138265,G,T,23,GENIC,homozygous,978017502 1,214139461,214139462,A,T,29,GENIC,homozygous,978017503 1,214140827,214140828,G,T,32,GENIC,homozygous,978017504 1,214142890,214142891,A,G,48,GENIC,homozygous,978017505 1,214146027,214146028,T,C,35,GENIC,homozygous,978017506 1,214146950,214146951,G,A,51,GENIC,homozygous,978017507