chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	4770889	4770890	T	C	30	GENIC	possibly homozygous	72977373
3	4771153	4771154	C	T	22	GENIC	homozygous	72977376
3	4771157	4771158	C	T	22	GENIC	homozygous	71704504
3	4771390	4771391	A	G	18	GENIC	homozygous	71704510
3	4771441	4771442	G	A	19	GENIC	homozygous	72977379
3	4772458	4772459	T	C	25	GENIC	homozygous	72977382
3	4773774	4773775	C	T	28	GENIC	possibly homozygous	71704513
3	4774492	4774493	T	C	21	GENIC	homozygous	71704516
3	4778492	4778493	A	G	18	GENIC	possibly homozygous	71704522
3	4778958	4778959	A	C	21	GENIC	homozygous	71704528
3	4779619	4779620	C	A	21	GENIC	homozygous	71704535
3	4779750	4779751	A	T	15	GENIC	homozygous	71704538
3	4778604	4778605	C	G	17	GENIC	homozygous	74628470
3	4778606	4778607	C	G	16	GENIC	homozygous	74628472
3	4778608	4778609	C	G	15	GENIC	homozygous	74628475
3	4778612	4778613	C	G	14	GENIC	homozygous	74628477
3	4778614	4778615	C	G	14	GENIC	homozygous	74628480