chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2546669	2546670	A	G	32	GENIC	homozygous	115234638
12	2546780	2546781	G	A	33	GENIC	homozygous	115234640
12	2546917	2546918	C	T	44	GENIC	homozygous	115357470
12	2547111	2547112	G	A	37	GENIC	homozygous	115234642
12	2548161	2548162	G	A	30	GENIC	homozygous	115234644
12	2548421	2548422	A	T	12	GENIC	homozygous	115357471
12	2548447	2548448	G	A	12	GENIC	homozygous	115234646
12	2548526	2548527	C	T	32	GENIC	homozygous	115234648
12	2548637	2548638	G	A	38	GENIC	homozygous	115234650
12	2549644	2549645	C	T	29	GENIC	homozygous	115234652
12	2549904	2549905	G	A	32	GENIC	homozygous	115234654
12	2551362	2551363	C	T	15	GENIC	homozygous	115357472
12	2551511	2551512	T	C	34	GENIC	homozygous	115357473
12	2551912	2551913	T	C	27	GENIC	homozygous	115357474
12	2554177	2554178	A	G	23	GENIC	homozygous	115234660
12	2555000	2555001	G	C	5	GENIC	homozygous	115234666
12	2555259	2555260	C	T	41	GENIC	homozygous	115357476