chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2069706	2069707	G	A	20	GENIC	homozygous	115233558
12	2070044	2070045	T	C	21	GENIC	homozygous	115233560
12	2071647	2071648	G	C	26	GENIC	homozygous	115233562
12	2071700	2071701	G	A	27	GENIC	homozygous	115233564
12	2071900	2071901	T	C	18	GENIC	homozygous	115233566
12	2072117	2072118	T	C	30	GENIC	homozygous	115233568
12	2072264	2072265	T	C	21	GENIC	homozygous	115233570
12	2072899	2072900	T	G	37	GENIC	homozygous	115233572
12	2073357	2073358	G	C	41	GENIC	homozygous	115357226
12	2073664	2073665	C	A	36	GENIC	homozygous	115233574
12	2073739	2073740	T	C	29	GENIC	possibly homozygous	115233576
12	2075128	2075129	G	T	18	GENIC	homozygous	115233580
12	2077457	2077458	T	A	31	GENIC	homozygous	115233582
12	2085079	2085080	A	T	27	GENIC	possibly homozygous	115233584
12	2089791	2089792	A	G	11	GENIC	homozygous	115233586
12	2093373	2093374	C	T	40	GENIC	homozygous	115233588
12	2096896	2096897	G	A	20	GENIC	homozygous	115233590