chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	9694942	9694943	C	T	48	GENIC	homozygous	140402075
19	9695644	9695645	T	C	57	GENIC	possibly homozygous	147184715
19	9695852	9695853	C	T	52	GENIC	possibly homozygous	147184716
19	9697082	9697083	A	G	56	GENIC	homozygous	147184717
19	9697490	9697491	A	G	16	GENIC	homozygous	147377748
19	9697542	9697543	T	C	20	GENIC	homozygous	147377749
19	9697574	9697575	A	G	25	GENIC	homozygous	147377750
19	9697604	9697605	T	C	27	GENIC	homozygous	147377751
19	9697657	9697658	G	C	31	GENIC	homozygous	147184718
19	9698205	9698206	G	A	53	GENIC	homozygous	147184719
19	9698621	9698622	C	T	44	GENIC	homozygous	147184720
19	9698708	9698709	C		49	GENIC	homozygous	147171132
19	9698453	9698458	GGCTC		43	GENIC	homozygous	147171130
19	9698647	9698647		G	45	GENIC	homozygous	147171131
19	9698819	9698820	A	G	52	GENIC	homozygous	140402077
19	9698829	9698830	C	T	51	GENIC	homozygous	147184721
19	9699036	9699037	C	T	36	GENIC	homozygous	147184722
19	9699319	9699319		AGAGACAG	35	GENIC	homozygous	147171133
19	9699341	9699341		AC	33	GENIC	homozygous	147171134
19	9701634	9701635	T	G	50	GENIC	possibly homozygous	140402081
19	9697542	9697543	T		20	GENIC	heterozygous	404100454
19	9697574	9697575	A		25	GENIC	heterozygous	404100455
19	9697604	9697605	T		27	GENIC	heterozygous	404100456