chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,153555542,153555543,T,G,7,GENIC,homozygous,989778495 X,153594385,153594386,C,G,3,GENIC,homozygous,989778496 X,153598653,153598654,G,T,4,GENIC,homozygous,989778497 X,153598681,153598682,G,T,9,GENIC,homozygous,989778498 X,153598807,153598808,G,A,5,GENIC,homozygous,989778499 X,153598810,153598811,C,A,4,GENIC,homozygous,989778500 X,153598870,153598871,C,A,9,GENIC,homozygous,989778501 X,153602136,153602137,C,T,7,GENIC,homozygous,989778502 X,153602157,153602158,C,T,3,GENIC,homozygous,989778503 X,153602220,153602221,C,T,2,GENIC,homozygous,989778504 X,153646535,153646536,G,A,8,GENIC,homozygous,989778505 X,153646544,153646545,G,A,10,GENIC,homozygous,989778506 X,153692285,153692286,G,C,8,GENIC,homozygous,989778507 X,153755259,153755260,C,T,16,GENIC,homozygous,989778508 X,153755261,153755262,A,T,13,GENIC,homozygous,989778509 X,153772165,153772166,G,T,7,GENIC,homozygous,989778510 X,153836513,153836514,T,G,4,GENIC,homozygous,989778511