chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 10,59306517,59306518,A,C,24,GENIC,homozygous,558760807 10,59306518,59306519,T,TA,24,GENIC,homozygous,703706082 10,59308262,59308263,T,-,8,GENIC,homozygous,703706083 10,59308366,59308367,A,T,7,GENIC,homozygous,557012686 10,59308493,59308494,A,G,18,GENIC,homozygous,557012687 10,59308867,59308868,A,AACACAC,3,GENIC,heterozygous,703706087 10,59309038,59309039,G,A,20,GENIC,homozygous,557012688 10,59309136,59309137,C,T,23,GENIC,homozygous,557012689 10,59310029,59310030,C,A,24,GENIC,homozygous,557012690 10,59310380,59310381,A,G,47,GENIC,homozygous,557012691 10,59310717,59310718,T,C,28,GENIC,homozygous,557012692 10,59310868,59310869,C,T,28,GENIC,homozygous,557012693 10,59311552,59311553,C,G,8,GENIC,homozygous,557012694 10,59311721,59311722,T,TACACAC,6,GENIC,homozygous,703706089 10,59311924,59311925,C,T,27,GENIC,homozygous,557012695 10,59312489,59312490,G,A,23,GENIC,homozygous,557012696 10,59312928,59312929,T,C,15,GENIC,homozygous,557012697 10,59313114,59313115,T,C,18,GENIC,homozygous,557012698 10,59313531,59313532,T,C,18,GENIC,homozygous,557012699 10,59314557,59314558,G,A,27,GENIC,homozygous,557012700 10,59314949,59314950,A,G,21,GENIC,homozygous,557012701 10,59315564,59315565,T,C,22,GENIC,homozygous,557012702 10,59316014,59316015,C,CTCCTCCTCTTCT,5,GENIC,homozygous,703706090 10,59317242,59317243,C,-,27,GENIC,homozygous,703706092 10,59320139,59320140,G,A,21,GENIC,homozygous,557012703