chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41155803	41155804	G	C	28	GENIC	homozygous	126263056
12	41157954	41157955	A	G	11	GENIC	homozygous	126173444
12	41162836	41162837	G	T	16	GENIC	homozygous	126263057
12	41162985	41162986	C	T	6	GENIC	heterozygous	126173484
12	41163110	41163111	A	G	21	GENIC	heterozygous	126173485
12	41163117	41163118	C	T	25	GENIC	heterozygous	126263058
12	41163230	41163231	G	A	30	GENIC	heterozygous	126263059
12	41163263	41163264	T	A	19	GENIC	heterozygous	126249579
12	41163303	41163304	A	G	10	GENIC	homozygous	126263060
12	41163609	41163610	C	A	4	GENIC	homozygous	126263061
12	41163880	41163881	C	A	13	GENIC	homozygous	126173486
12	41164101	41164102	T	C	20	GENIC	homozygous	126173487
12	41164367	41164368	G	A	26	GENIC	homozygous	126263062
12	41164751	41164752	G	A	14	GENIC	homozygous	126173488
12	41164889	41164890	T	C	21	GENIC	homozygous	126173489
12	41165150	41165151	A	G	16	GENIC	homozygous	126173490
12	41165420	41165421	C	G	11	GENIC	heterozygous	126263063
12	41165493	41165494	A	G	5	GENIC	homozygous	126263064
12	41165696	41165697	G	A	13	GENIC	heterozygous	126173492
12	41166080	41166081	T	A	5	GENIC	heterozygous	126214775
12	41166197	41166198	C	T	17	GENIC	heterozygous	126173493
12	41166355	41166356	A	G	13	GENIC	heterozygous	126263065
12	41166382	41166383	G	A	9	GENIC	heterozygous	126173496
12	41166563	41166564	G	C	12	GENIC	heterozygous	126173497
12	41167127	41167128	G	A	14	GENIC	homozygous	126263066