chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	205179364	205179365	T	C	7	GENIC	homozygous	61064317
1	205179394	205179395	G	A	8	GENIC	homozygous	61064318
1	205179638	205179639	A	G	27	GENIC	possibly homozygous	61064319
1	205179719	205179720	T	C	22	GENIC	homozygous	61064320
1	205180756	205180757	C	G	8	GENIC	homozygous	61064323
1	205181519	205181520	G	C	22	GENIC	possibly homozygous	61064324
1	205182931	205182932	C	A	17	GENIC	possibly homozygous	61064329
1	205183648	205183649	T	C	12	GENIC	homozygous	61064331
1	205183751	205183752	C	T	22	GENIC	possibly homozygous	61064332
1	205183972	205183973	A	C	9	GENIC	heterozygous	61064333
1	205184054	205184055	T	G	13	GENIC	possibly homozygous	61064335
1	205184362	205184363	C	A	19	GENIC	possibly homozygous	61064336
1	205185132	205185139	TTTTTTG	-------	3	GENIC	heterozygous	61064343
1	205185254	205185255	A	G	24	GENIC	homozygous	61064346
1	205185462	205185463	G	T	12	GENIC	possibly homozygous	61064348
1	205186000	205186001	T	C	16	GENIC	possibly homozygous	61064351
1	205186601	205186602	G	T	29	GENIC	possibly homozygous	61064352
1	205187334	205187335	T	TA	7	GENIC	homozygous	61064353
1	205187819	205187820	G	GGGA	2	GENIC	homozygous	61064354
1	205188054	205188055	T	C	8	GENIC	possibly homozygous	61064356
1	205188274	205188281	CTTCTAT	-------	2	GENIC	homozygous	61064357
1	205188547	205188548	G	A	16	GENIC	possibly homozygous	61064358