chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	103521956	103521957	T	TA	11	GENIC	homozygous	51269456
13	103522214	103522215	G	-	9	GENIC	homozygous	51269457
13	103523118	103523119	C	T	16	GENIC	homozygous	49872694
13	103523372	103523373	G	A	20	GENIC	homozygous	51269458
13	103523870	103523871	G	A	7	GENIC	homozygous	51269459
13	103524304	103524308	CTCA	----	13	GENIC	homozygous	51269460
13	103524358	103524359	C	T	18	GENIC	possibly homozygous	51269461
13	103524700	103524701	G	A	8	GENIC	homozygous	51269462
13	103525757	103525758	G	A	11	GENIC	homozygous	51269463
13	103525975	103525976	G	A	14	GENIC	homozygous	49872699
13	103526655	103526656	T	C	15	GENIC	homozygous	49872700
13	103528159	103528160	C	T	7	GENIC	homozygous	51269464
13	103528280	103528281	A	G	10	GENIC	homozygous	49872706
13	103528336	103528337	G	A	9	GENIC	homozygous	51269465
13	103528580	103528581	G	A	10	GENIC	homozygous	51269466
13	103529667	103529668	G	GA	17	GENIC	homozygous	51269467
13	103529761	103529762	A	G	14	GENIC	homozygous	49872708
13	103531236	103531237	G	A	11	GENIC	homozygous	51269468
13	103535336	103535337	G	A	16	GENIC	homozygous	51269469
13	103539837	103539838	G	C	10	GENIC	homozygous	51269470
13	103535663	103535664	T	C	14	GENIC	homozygous	49872717
13	103537529	103537530	T	C	9	GENIC	homozygous	49872721
13	103539836	103539837	T	C	10	GENIC	homozygous	49872723
13	103539838	103539839	T	C	10	GENIC	homozygous	49872724
13	103539989	103539991	AC	--	7	GENIC	homozygous	51269471
13	103541194	103541195	T	C	9	GENIC	homozygous	49872727
13	103542177	103542178	C	T	11	GENIC	homozygous	51269472
13	103542931	103542932	C	T	11	GENIC	homozygous	51269473