chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,105293208,105293209,A,G,8,GENIC,homozygous,792134042 X,105293226,105293227,G,A,8,GENIC,homozygous,792134043 X,105293276,105293277,G,A,10,GENIC,homozygous,792134044 X,105293666,105293667,C,A,6,GENIC,homozygous,792134045 X,105293676,105293677,G,C,7,GENIC,homozygous,792134046 X,105294042,105294043,A,G,2,GENIC,homozygous,792134047 X,105296887,105296888,T,A,7,GENIC,homozygous,792134048 X,105297118,105297119,C,T,7,GENIC,homozygous,792134049 X,105297905,105297906,T,A,6,GENIC,homozygous,792134050 X,105301990,105301991,G,T,5,GENIC,homozygous,792134051 X,105302163,105302164,C,A,4,GENIC,homozygous,792134052 X,105302184,105302185,T,C,6,GENIC,homozygous,792134053 X,105302210,105302211,C,A,6,GENIC,homozygous,792134054 X,105303915,105303916,A,G,10,GENIC,homozygous,792134055