chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	66090176	66090177	A	G	36	GENIC	homozygous	46190903
19	66090264	66090265	T	C	54	GENIC	homozygous	46190904
19	66090766	66090767	C	T	48	GENIC	possibly homozygous	46190905
19	66090845	66090846	T	C	55	GENIC	homozygous	46190906
19	66091187	66091188	A	G	56	GENIC	homozygous	46190907
19	66091428	66091429	C	CAG	48	GENIC	homozygous	46190908
19	66091743	66091744	G	A	59	GENIC	homozygous	46190909
19	66091820	66091821	A	G	67	GENIC	homozygous	46190910
19	66091840	66091841	C	G	68	GENIC	possibly homozygous	46190911
19	66092098	66092099	G	GTT	19	GENIC	heterozygous	46190912
19	66092098	66092099	G	GTTT	19	GENIC	heterozygous	46216591
19	66092111	66092112	G	-	32	GENIC	heterozygous	46216592
19	66092736	66092737	T	-	5	GENIC	homozygous	46190913
19	66092793	66092794	A	G	47	GENIC	homozygous	46190914