chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	10304111	10304112	G	T	28	GENIC	homozygous	68593285
7	10307821	10307822	A	T	44	GENIC	homozygous	68593295
7	10309015	10309016	C	T	32	GENIC	possibly homozygous	68593297
7	10309664	10309665	T	G	50	GENIC	homozygous	68593299
7	10310150	10310151	T	C	29	GENIC	homozygous	68593302
7	10311768	10311769	G	A	47	GENIC	homozygous	68593304
7	10312834	10312835	C	T	41	GENIC	homozygous	68593306
7	10314595	10314596	A	G	24	GENIC	homozygous	68593308
7	10317573	10317574	C	T	24	GENIC	homozygous	68593310
7	10318049	10318050	A	G	45	GENIC	homozygous	68593312
7	10318190	10318191	G	A	24	GENIC	possibly homozygous	68593316
7	10318732	10318733	C	A	30	GENIC	homozygous	68593318
7	10318780	10318781	C	T	26	GENIC	homozygous	68593320
7	10320139	10320140	T	C	44	GENIC	homozygous	68593321
7	10321758	10321759	C	G	33	GENIC	homozygous	68593323
7	10321768	10321769	C	T	33	GENIC	homozygous	68593325
7	10322050	10322051	G	T	24	GENIC	homozygous	68593327
7	10322195	10322196	A	G	30	GENIC	homozygous	68593329
7	10322487	10322488	A	G	47	GENIC	homozygous	68593331
7	10324192	10324193	A	G	29	GENIC	homozygous	68593333
7	10324320	10324321	T	C	20	GENIC	homozygous	68593335