chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	74698139	74698140	C	T	45	GENIC	possibly homozygous	117064990
10	74700618	74700619	G	A	42	GENIC	possibly homozygous	117064992
10	74701022	74701023	C	A	46	GENIC	homozygous	117064994
10	74701584	74701585	G	A	37	GENIC	homozygous	117064996
10	74706197	74706198	A	T	36	GENIC	homozygous	117064998
10	74706509	74706510	T	C	44	GENIC	homozygous	117065000
10	74706514	74706515	G	A	46	GENIC	homozygous	117065002
10	74706828	74706829	T	C	39	GENIC	homozygous	118001492
10	74706863	74706864	G	A	31	GENIC	possibly homozygous	118001493
10	74706869	74706870	G	A	32	GENIC	possibly homozygous	118001494
10	74708146	74708147	A	T	28	GENIC	homozygous	116637544
10	74709597	74709598	A	G	62	GENIC	homozygous	116637546
10	74709958	74709959	G	A	38	GENIC	homozygous	116637548
10	74710444	74710445	G	A	49	GENIC	homozygous	116637550
10	74710863	74710864	T	C	44	GENIC	homozygous	116637554
10	74711174	74711175	A	C	34	GENIC	homozygous	116637556
10	74712202	74712203	T	C	29	GENIC	homozygous	117065004
10	74712234	74712235	G	T	33	GENIC	possibly homozygous	117065006
10	74712596	74712597	G	C	54	GENIC	homozygous	116637558
10	74713384	74713385	A	G	39	GENIC	homozygous	116637560
10	74713892	74713893	G	T	52	GENIC	possibly homozygous	116637562
10	74715051	74715052	G	A	45	GENIC	possibly homozygous	116637564
10	74717018	74717019	G	A	38	GENIC	homozygous	117065008
10	74718727	74718728	C	A	57	GENIC	homozygous	117065010
10	74718815	74718816	T	C	44	GENIC	homozygous	116637572
10	74718931	74718932	A	G	39	GENIC	homozygous	117065012
10	74719678	74719679	T	A	24	GENIC	homozygous	116637574
10	74720111	74720112	T	C	57	GENIC	homozygous	116637576
10	74720372	74720373	A	G	44	GENIC	homozygous	117065014
10	74721213	74721214	T	C	30	GENIC	possibly homozygous	118001497
10	74707856	74707857	C	T	31	GENIC	homozygous	117313024