chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	73179946	73179947	G	A	17	GENIC	homozygous	108867007
1	73181582	73181583	A	G	17	GENIC	homozygous	108867008
1	73181645	73181646	T	C	19	GENIC	homozygous	108867009
1	73182097	73182098	C	G	32	GENIC	homozygous	108867010
1	73182183	73182184	A	G	30	GENIC	homozygous	108867011
1	73182769	73182770	G	A	31	GENIC	possibly homozygous	108867012
1	73183017	73183018	T	A	10	GENIC	homozygous	108867013
1	73209236	73209237	G	A	13	GENIC	homozygous	108133429
1	73216392	73216393	A	T	22	GENIC	homozygous	108867015
1	73216943	73216944	A	T	21	GENIC	homozygous	108867017
1	73222771	73222772	T	A	10	GENIC	homozygous	108867018
1	73222864	73222865	C	T	32	GENIC	homozygous	108867019
1	73224027	73224028	T	C	21	GENIC	homozygous	108867020
1	73224168	73224169	A	G	22	GENIC	homozygous	108867021
1	73224288	73224289	T	C	27	GENIC	possibly homozygous	108867022
1	73224320	73224321	G	A	18	GENIC	homozygous	108867023
1	73224858	73224859	T	C	20	GENIC	homozygous	108867024
1	73225506	73225507	T	C	29	GENIC	homozygous	108867025
1	73225976	73225977	A	G	24	GENIC	homozygous	108867026