chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	150637696	150637697	T	C	17	GENIC	homozygous	113182414
4	150638213	150638214	A	G	18	GENIC	homozygous	112884481
4	150638432	150638433	A	G	16	GENIC	homozygous	113182415
4	150638559	150638560	C	T	20	GENIC	homozygous	113182416
4	150638851	150638852	C	A	7	GENIC	heterozygous	126102155
4	150639001	150639002	C	T	23	GENIC	homozygous	113182420
4	150639757	150639758	A	G	16	GENIC	homozygous	113182421
4	150640529	150640530	T	G	16	GENIC	heterozygous	112884483
4	150640921	150640922	C	T	24	GENIC	homozygous	112884485
4	150641793	150641794	C	T	5	GENIC	homozygous	113182422
4	150642933	150642934	C	A	13	GENIC	homozygous	113182423
4	150643206	150643207	G	T	6	GENIC	homozygous	113182424
4	150643222	150643223	G	A	13	GENIC	homozygous	113182425
4	150643322	150643323	C	T	15	GENIC	homozygous	113182426
4	150643450	150643451	A	T	17	GENIC	homozygous	112884489
4	150643517	150643518	G	A	19	GENIC	homozygous	113182427
4	150643841	150643842	A	C	21	GENIC	homozygous	112884490
4	150643843	150643844	A	G	18	GENIC	homozygous	112884491
4	150643882	150643883	C	T	25	GENIC	homozygous	112884492
4	150643989	150643990	C	T	20	GENIC	homozygous	113182428
4	150644186	150644187	G	A	16	GENIC	homozygous	113182429
4	150644429	150644430	A	G	17	GENIC	homozygous	112884496
4	150644448	150644449	C	T	11	GENIC	homozygous	113182430
4	150644789	150644790	G	A	13	GENIC	homozygous	113182431
4	150645227	150645228	G	A	11	GENIC	homozygous	112884499
4	150645481	150645482	T	C	10	GENIC	homozygous	112884502