chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	4770889	4770890	T	C	17	GENIC	possibly homozygous	72977373
3	4771149	4771150	C	T	32	GENIC	possibly homozygous	79862769
3	4771153	4771154	C	T	29	GENIC	homozygous	72977376
3	4771157	4771158	C	T	27	GENIC	homozygous	71704504
3	4771390	4771391	A	G	24	GENIC	homozygous	71704510
3	4771441	4771442	G	A	24	GENIC	homozygous	72977379
3	4772458	4772459	T	C	13	GENIC	homozygous	72977382
3	4773774	4773775	C	T	22	GENIC	homozygous	71704513
3	4774492	4774493	T	C	21	GENIC	possibly homozygous	71704516
3	4775110	4775111	T	C	21	GENIC	possibly homozygous	72977385
3	4778492	4778493	A	G	30	GENIC	possibly homozygous	71704522
3	4778958	4778959	A	C	18	GENIC	heterozygous	71704528
3	4779619	4779620	C	A	16	GENIC	homozygous	71704535
3	4779750	4779751	A	T	17	GENIC	homozygous	71704538