chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 5,57028775,57028776,G,C,69,GENIC,homozygous,978986944 5,57030477,57030478,T,C,22,GENIC,homozygous,978986945 5,57030720,57030721,T,G,6,GENIC,homozygous,978986946 5,57030931,57030932,G,A,11,GENIC,homozygous,978986947 5,57030942,57030943,A,G,17,GENIC,homozygous,978986948 5,57031177,57031178,G,T,16,GENIC,homozygous,978986949 5,57031624,57031625,A,G,16,GENIC,homozygous,978986950 5,57031766,57031767,G,A,9,GENIC,homozygous,978986951 5,57032209,57032210,T,C,17,GENIC,homozygous,978986952 5,57032479,57032480,T,C,33,GENIC,homozygous,978986953 5,57033573,57033574,G,A,11,GENIC,homozygous,978986954 5,57033958,57033959,T,C,42,GENIC,homozygous,978986955 5,57034277,57034278,T,C,24,GENIC,homozygous,978986956 5,57034397,57034398,A,G,26,GENIC,homozygous,978986957 5,57034409,57034410,G,A,28,GENIC,homozygous,978986958 5,57034825,57034826,C,G,13,GENIC,homozygous,978986959 5,57035682,57035683,T,C,46,GENIC,homozygous,978986960 5,57035743,57035744,A,G,41,GENIC,possibly homozygous,978986961 5,57036058,57036059,C,T,24,GENIC,homozygous,978986962 5,57036421,57036422,G,A,16,GENIC,homozygous,978986963 5,57036500,57036501,C,T,18,GENIC,homozygous,978986964 5,57037152,57037153,C,T,10,GENIC,homozygous,978986965 5,57037225,57037226,G,A,15,GENIC,homozygous,978986966 5,57037504,57037505,G,A,17,GENIC,homozygous,978986967 5,57037612,57037613,T,C,17,GENIC,homozygous,978986968 5,57037878,57037879,C,G,25,GENIC,homozygous,978986969 5,57037885,57037886,C,T,28,GENIC,homozygous,978986970 5,57038528,57038529,C,T,20,GENIC,homozygous,978986971