chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	37668749	37668750	A	G	2	GENIC	homozygous	115321201
12	37668751	37668752	A	G	2	GENIC	homozygous	115321203
12	37668841	37668841		C	2	GENIC	homozygous	128986167
12	37668846	37668846		C	2	GENIC	homozygous	128986168
12	37668801	37668801		G	2	GENIC	homozygous	128986165
12	37668824	37668825	T		2	GENIC	homozygous	128986166
12	37668856	37668856		C	2	GENIC	homozygous	128986169
12	37668869	37668869		C	2	GENIC	homozygous	128986170
12	37668911	37668912	T		2	GENIC	homozygous	128986171
12	37668916	37668917	A		3	GENIC	homozygous	128986172
12	37668920	37668921	G		3	GENIC	homozygous	128986173
12	37668926	37668927	C		3	GENIC	homozygous	128986174
12	37668939	37668940	G		4	GENIC	homozygous	128986175
12	37668951	37668952	A		4	GENIC	homozygous	128986176
12	37668968	37668968		GG	4	GENIC	homozygous	128986177
12	37668988	37668990	GT		4	GENIC	homozygous	128986178
12	37668998	37668998		G	5	GENIC	homozygous	128986179
12	37669045	37669046	T	C	5	GENIC	homozygous	115321205
12	37668850	37668851	G	C	2	GENIC	homozygous	115525352
12	37671749	37671750	T	C	17	GENIC	homozygous	115321207
12	37672994	37672995	C	G	17	GENIC	homozygous	115321209
12	37673499	37673500	T	C	20	GENIC	homozygous	115321211
12	37673924	37673925	T	C	38	GENIC	homozygous	115321213
12	37674255	37674256	T	C	29	GENIC	heterozygous	115525354
12	37674910	37674911	T	A	14	GENIC	possibly homozygous	115321215
12	37676601	37676602	A	T	29	GENIC	heterozygous	115525356