chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 7,145146563,145146564,T,C,7,GENIC,homozygous,1000791552 7,145147728,145147729,C,A,6,GENIC,homozygous,1000791553 7,145148101,145148102,A,G,9,GENIC,homozygous,1000791554 7,145148126,145148127,A,G,7,GENIC,homozygous,1000791555 7,145148400,145148401,T,C,2,GENIC,homozygous,1000791556 7,145149929,145149930,G,A,9,GENIC,homozygous,1000791557 7,145149955,145149956,T,C,11,GENIC,homozygous,1000791558 7,145150310,145150311,C,A,5,GENIC,homozygous,1000791559 7,145150986,145150987,T,C,6,GENIC,homozygous,1000791560 7,145151089,145151090,G,C,2,GENIC,homozygous,1000791561 7,145151090,145151091,C,T,2,GENIC,homozygous,1000791562 7,145151136,145151137,T,C,2,GENIC,homozygous,1000791563 7,145151185,145151186,T,C,4,GENIC,homozygous,1000791564 7,145151315,145151316,G,C,3,GENIC,homozygous,1000791565 7,145151424,145151425,G,C,3,GENIC,homozygous,1000791566 7,145152460,145152461,T,C,8,GENIC,homozygous,1000791567 7,145152860,145152861,G,C,4,GENIC,homozygous,1000791568