chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	133415966	133415967	A	G	35	GENIC	homozygous	112832623
4	133416503	133416504	A	G	34	GENIC	homozygous	112832624
4	133416540	133416541	T	C	44	GENIC	homozygous	112832625
4	133416709	133416710	A	G	20	GENIC	homozygous	112832626
4	133416776	133416777	A	G	24	GENIC	homozygous	112832627
4	133416951	133416952	G	T	21	GENIC	homozygous	112832628
4	133417267	133417268	T	C	28	GENIC	homozygous	112832629
4	133417273	133417274	T	C	25	GENIC	homozygous	112832630
4	133417336	133417337	A	G	28	GENIC	homozygous	112832631
4	133417387	133417388	C	T	23	GENIC	homozygous	112832632
4	133417493	133417494	A	C	19	GENIC	homozygous	112832633
4	133417501	133417502	G	A	20	GENIC	homozygous	112832634
4	133417502	133417503	T	C	21	GENIC	homozygous	112832635
4	133417579	133417580	T	C	20	GENIC	homozygous	112832636
4	133419399	133419400	C	T	25	GENIC	homozygous	112832638
4	133419929	133419930	C	A	14	GENIC	homozygous	112832641
4	133420153	133420154	C	G	22	GENIC	homozygous	112832642
4	133420256	133420257	C	G	37	GENIC	homozygous	112832643
4	133420330	133420331	T	C	29	GENIC	homozygous	112832644
4	133420418	133420419	C	A	28	GENIC	homozygous	112832645
4	133420421	133420422	C	A	30	GENIC	homozygous	113306524