chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 10,69766778,69766779,T,C,3,GENIC,homozygous,675911889 10,69767520,69767524,TGTC,----,6,GENIC,homozygous,771682971 10,69772257,69772258,C,A,9,GENIC,homozygous,675911890 10,69772568,69772569,G,GA,5,GENIC,homozygous,771682972 10,69774006,69774007,G,A,10,GENIC,homozygous,675911891 10,69774032,69774033,C,CT,2,GENIC,homozygous,771682974 10,69775330,69775331,T,G,5,GENIC,homozygous,675911892 10,69776752,69776754,AA,--,4,GENIC,homozygous,771682975 10,69776816,69776817,T,A,8,GENIC,homozygous,675911893 10,69777797,69777798,G,A,6,GENIC,homozygous,675911894 10,69779596,69779598,CA,--,7,GENIC,heterozygous,771682977 10,69782003,69782004,A,G,7,GENIC,homozygous,675911895 10,69782440,69782441,T,C,3,GENIC,homozygous,675911896 10,69786953,69786954,T,C,5,GENIC,homozygous,675911897 10,69787207,69787208,T,C,8,GENIC,homozygous,675911898 10,69787269,69787271,TC,--,6,GENIC,homozygous,771682978 10,69787470,69787471,A,G,8,GENIC,homozygous,675911899 10,69787925,69787926,T,C,4,GENIC,homozygous,675911900 10,69788151,69788152,C,T,3,GENIC,homozygous,675911901