chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 19,14653806,14653807,G,A,20,GENIC,homozygous,974247995 19,14654618,14654619,C,T,22,GENIC,homozygous,974247996 19,14654824,14654825,G,A,28,GENIC,homozygous,974247997 19,14654826,14654827,G,A,29,GENIC,homozygous,974247998 19,14656129,14656130,C,T,28,GENIC,homozygous,974247999 19,14656676,14656677,G,A,33,GENIC,homozygous,974248000 19,14657553,14657554,A,G,26,GENIC,homozygous,974248001 19,14657578,14657579,C,T,28,GENIC,homozygous,974248002 19,14658363,14658364,T,C,20,GENIC,homozygous,974248003 19,14659257,14659258,C,T,30,GENIC,homozygous,974248004 19,14659347,14659348,G,A,29,GENIC,homozygous,974248005 19,14659420,14659421,A,G,37,GENIC,homozygous,974248006 19,14659588,14659589,C,T,29,GENIC,homozygous,974248007 19,14660318,14660319,G,A,38,GENIC,homozygous,974248008 19,14661428,14661429,T,A,30,GENIC,homozygous,974248009 19,14662496,14662497,A,G,29,GENIC,homozygous,974248010 19,14662927,14662928,T,C,26,GENIC,homozygous,974248011 19,14663545,14663546,A,G,22,GENIC,homozygous,974248012