chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41201577	41201578	C	G	18	GENIC	homozygous	115384697
12	41201578	41201579	C	T	17	GENIC	homozygous	115384699
12	41201579	41201580	A	G	17	GENIC	homozygous	115384701
12	41203691	41203692	C	G	18	GENIC	homozygous	115329618
12	41204070	41204071	T	C	30	GENIC	homozygous	115329620
12	41204226	41204227	G	A	28	GENIC	homozygous	115329622
12	41204242	41204243	G	A	31	GENIC	homozygous	115329624
12	41204603	41204604	T	C	26	GENIC	homozygous	115384711
12	41204753	41204754	T	C	24	GENIC	homozygous	115329626
12	41204785	41204786	T	A	22	GENIC	homozygous	115329628
12	41204978	41204979	G	A	27	GENIC	homozygous	115329630
12	41205091	41205092	G	A	32	GENIC	homozygous	115329632
12	41206413	41206414	G	C	17	GENIC	homozygous	115329634