chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	50377623	50377624	G	A	6	GENIC	homozygous	116590844
10	50377851	50377852	A	G	21	GENIC	homozygous	116590846
10	50378338	50378339	G	C	12	GENIC	homozygous	116590848
10	50380230	50380231	A	G	10	GENIC	homozygous	116590850
10	50380494	50380495	C	T	16	GENIC	homozygous	116590852
10	50387616	50387617	T	C	23	GENIC	homozygous	116590862
10	50388090	50388091	T	C	14	GENIC	homozygous	116590864
10	50389732	50389733	C	T	19	GENIC	homozygous	116590866
10	50390711	50390712	C	T	5	GENIC	homozygous	116590868
10	50391122	50391123	G	A	16	GENIC	homozygous	117178956
10	50391742	50391743	G	A	23	GENIC	homozygous	116590870
10	50392081	50392082	T	G	20	GENIC	homozygous	126382326
10	50393121	50393122	T	C	16	GENIC	homozygous	116590872
10	50394037	50394038	T	G	8	GENIC	homozygous	116590874
10	50394516	50394517	A	G	9	GENIC	homozygous	117254172
10	50394558	50394559	A	C	8	GENIC	homozygous	126382327
10	50396605	50396606	G	T	16	GENIC	homozygous	116590876
10	50396626	50396627	C	T	11	GENIC	homozygous	116590878
10	50396985	50396986	A	G	5	GENIC	homozygous	116590880
10	50398310	50398311	C	G	12	GENIC	homozygous	116590882
10	50398731	50398732	C	G	10	GENIC	homozygous	116590884
10	50399192	50399193	C	T	25	GENIC	homozygous	116590886
10	50399703	50399704	C	T	14	GENIC	homozygous	116590888
10	50400234	50400235	T	C	19	GENIC	homozygous	116590890
10	50400303	50400304	C	A	18	GENIC	homozygous	116590892
10	50400483	50400484	A	C	12	GENIC	homozygous	116590894
10	50401149	50401150	A	G	14	GENIC	homozygous	116590896