chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	48570884	48570885	T	A	35	GENIC	heterozygous	118036832
10	48571334	48571335	T	C	54	GENIC	homozygous	117009212
10	48571582	48571583	C	T	60	GENIC	homozygous	117009213
10	48571586	48571587	A	G	58	GENIC	homozygous	116879966
10	48572109	48572110	T	C	42	GENIC	homozygous	118036833
10	48572765	48572766	C	T	49	GENIC	homozygous	117009214
10	48573661	48573662	C	T	78	GENIC	homozygous	116879968
10	48574155	48574156	T	C	57	GENIC	possibly homozygous	116879970
10	48574190	48574191	A	T	51	GENIC	homozygous	117009215
10	48574215	48574216	G	A	48	GENIC	homozygous	117009216
10	48574378	48574379	C	T	39	GENIC	homozygous	117009217
10	48574413	48574414	G	A	38	GENIC	homozygous	117009218
10	48574491	48574492	T	C	43	GENIC	possibly homozygous	117009219
10	48575353	48575354	A	G	57	GENIC	homozygous	117009220
10	48576596	48576597	G	A	49	GENIC	homozygous	117009221
10	48576975	48576976	T	C	62	GENIC	homozygous	116879976
10	48577034	48577035	A	G	52	GENIC	homozygous	116879978
10	48577601	48577602	G	A	48	GENIC	homozygous	117009222
10	48579232	48579233	C	T	77	GENIC	possibly homozygous	117009223
10	48580398	48580399	C	G	57	GENIC	homozygous	116879980
10	48580825	48580826	G	T	41	GENIC	homozygous	116879982
10	48580993	48580994	A	T	51	GENIC	homozygous	118036834
10	48581078	48581079	T	G	48	GENIC	homozygous	117009224
10	48582499	48582500	A	G	69	GENIC	possibly homozygous	117009225
10	48582771	48582772	C	T	61	GENIC	homozygous	116879989
10	48584808	48584809	T	C	63	GENIC	homozygous	116879991
10	48585493	48585494	G	A	62	GENIC	homozygous	116879993
10	48585588	48585589	C	T	66	GENIC	homozygous	117009226