chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14560752	14560753	C	-	14	GENIC	heterozygous	51982655
10	14567890	14567891	C	CGTGT	7	GENIC	heterozygous	52431615
10	14567891	14567893	GT	--	7	GENIC	heterozygous	52431617
10	14575698	14575699	T	TG	15	GENIC	heterozygous	51329672
10	14575698	14575699	T	TGG	15	GENIC	heterozygous	51329673
10	14589849	14589850	A	ATG	8	GENIC	possibly homozygous	52356698
10	14590431	14590432	A	G	42	GENIC	homozygous	51329676
10	14591077	14591078	A	AT	36	GENIC	homozygous	51329677
10	14591307	14591308	C	T	51	GENIC	homozygous	51329679
10	14591817	14591818	T	C	37	GENIC	homozygous	51329680
10	14592023	14592024	C	T	33	GENIC	homozygous	51329681
10	14592303	14592307	CACA	----	3	GENIC	homozygous	52356700
10	14593990	14593991	A	G	33	GENIC	homozygous	51329683
10	14593992	14593994	AC	--	33	GENIC	homozygous	51329684
10	14593995	14593996	C	A	34	GENIC	homozygous	51329685
10	14594070	14594071	A	G	39	GENIC	homozygous	51329686
10	14594696	14594697	T	C	36	GENIC	homozygous	51329688
10	14595138	14595139	G	A	35	GENIC	homozygous	51329689
10	14595648	14595649	G	A	37	GENIC	homozygous	51329690
10	14596924	14596925	G	A	39	GENIC	homozygous	51329692
10	14597260	14597261	G	T	44	GENIC	homozygous	51329693
10	14597624	14597625	C	T	61	GENIC	homozygous	51329695
10	14597709	14597710	C	CTAACACAG	45	GENIC	homozygous	51329696
10	14598511	14598513	AA	--	31	GENIC	homozygous	51329698
10	14600260	14600261	C	T	40	GENIC	homozygous	51329699
10	14601435	14601436	C	T	41	GENIC	homozygous	51329701
10	14603665	14603666	T	C	49	GENIC	homozygous	51329702
10	14603725	14603726	T	G	33	GENIC	homozygous	51329704
10	14604196	14604197	T	TG	15	GENIC	heterozygous	51329706