chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13091642	13091643	A	G	29	GENIC	homozygous	115259742
12	13092299	13092300	G	T	17	GENIC	homozygous	115259744
12	13092512	13092513	G	A	18	GENIC	homozygous	115259746
12	13092755	13092756	T	A	35	GENIC	homozygous	115259748
12	13096700	13096701	G	A	25	GENIC	homozygous	115259750
12	13098210	13098211	G	C	36	GENIC	homozygous	115259752
12	13099650	13099651	T	C	18	GENIC	homozygous	115259754
12	13102473	13102474	T	C	29	GENIC	homozygous	115259756
12	13103676	13103677	C	T	29	GENIC	homozygous	115259758
12	13103844	13103845	A	T	20	GENIC	homozygous	115259760
12	13104281	13104282	G	A	38	GENIC	homozygous	115259762
12	13105348	13105349	C	T	22	GENIC	homozygous	115416645
12	13105565	13105566	T	G	21	GENIC	homozygous	115259764
12	13105707	13105708	C	G	16	GENIC	homozygous	115259766
12	13107182	13107183	C	T	21	GENIC	homozygous	115259768
12	13107640	13107641	C	T	23	GENIC	homozygous	115259770
12	13109211	13109212	C	T	13	GENIC	homozygous	115259772
12	13109316	13109317	G	A	19	GENIC	homozygous	115259774
12	13110695	13110696	T	C	21	GENIC	homozygous	115259776
12	13111748	13111749	A	G	26	GENIC	homozygous	115416647