chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	63661928	63661929	A	ATG	12	GENIC	heterozygous	62226899
1	63661928	63661929	A	ATGTGTG	12	GENIC	possibly homozygous	62130145
1	63663049	63663051	TT	--	16	GENIC	homozygous	61872606
1	63664002	63664003	T	G	16	GENIC	homozygous	61872607
1	63665464	63665465	G	A	10	GENIC	homozygous	61872608
1	63665726	63665728	TT	--	2	GENIC	homozygous	61872609
1	63665967	63665968	C	A	15	GENIC	homozygous	61872610
1	63668656	63668657	T	C	26	GENIC	homozygous	61872611
1	63668896	63668897	A	G	10	GENIC	homozygous	61706404
1	63672517	63672518	G	C	20	GENIC	homozygous	61872612
1	63674425	63674426	C	T	18	GENIC	homozygous	61872613
1	63675336	63675337	A	C	16	GENIC	homozygous	61872614
1	63676840	63676841	A	G	14	GENIC	homozygous	61872615
1	63677348	63677349	T	C	1	GENIC	homozygous	60728887
1	63674296	63674297	T	-	7	GENIC	possibly homozygous	60728884
1	63677299	63677300	C	-	3	GENIC	homozygous	60728885
1	63677346	63677347	C	A	1	GENIC	homozygous	60728886
1	63679907	63679908	C	A	10	GENIC	homozygous	61872616
1	63681634	63681635	C	A	9	GENIC	homozygous	61872617
1	63685788	63685789	C	-	3	GENIC	homozygous	60728896
1	63688084	63688085	C	-	1	GENIC	homozygous	62226900
1	63689150	63689151	G	-	19	GENIC	heterozygous	62130148
1	63689682	63689683	G	T	12	GENIC	homozygous	61872619
1	63690135	63690136	A	-	2	GENIC	homozygous	61872620
1	63690711	63690712	G	A	19	GENIC	homozygous	61872621