chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 19,55954267,55954268,C,T,23,GENIC,homozygous,971370929 19,55954280,55954281,T,C,23,GENIC,homozygous,971370930 19,55954436,55954437,T,G,27,GENIC,homozygous,971370931 19,55955492,55955493,C,T,25,GENIC,homozygous,971370932 19,55955630,55955631,G,A,32,GENIC,homozygous,971370933 19,55956322,55956323,C,T,36,GENIC,homozygous,971370934 19,55956368,55956369,A,G,45,GENIC,homozygous,971370935 19,55956409,55956410,T,C,38,GENIC,homozygous,971370936 19,55956610,55956611,A,G,30,GENIC,homozygous,971370937 19,55957368,55957369,A,G,23,GENIC,homozygous,971370938 19,55959036,55959037,C,A,24,GENIC,homozygous,971370939 19,55962798,55962799,G,A,15,GENIC,homozygous,971370940 19,55969496,55969497,A,C,43,GENIC,homozygous,971370941 19,55969634,55969635,T,C,15,GENIC,homozygous,971370942 19,55970589,55970590,A,T,23,GENIC,homozygous,971370943 19,55970590,55970591,A,G,22,GENIC,homozygous,971370944 19,55970894,55970895,G,A,17,GENIC,homozygous,971370945 19,55971676,55971677,A,G,31,GENIC,homozygous,971370946 19,55972186,55972187,G,C,24,GENIC,homozygous,971370947 19,55974009,55974010,A,G,35,GENIC,homozygous,971370948 19,55977203,55977204,T,C,26,GENIC,homozygous,971370949