chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	207964192	207964193	G	A	19	GENIC	homozygous	59356818
2	207964761	207964762	C	CGGG	11	GENIC	possibly homozygous	59356819
2	207964761	207964762	C	CGG	11	GENIC	heterozygous	60585304
2	207968686	207968687	C	CT	12	GENIC	possibly homozygous	59356823
2	207969018	207969020	TT	--	6	GENIC	homozygous	59356824
2	207970065	207970067	GT	--	37	GENIC	homozygous	59356826
2	207970104	207970105	T	TGTGC	37	GENIC	homozygous	59356828
2	207970329	207970330	T	-	13	GENIC	heterozygous	59356829
2	207970759	207970760	C	CAA	7	GENIC	heterozygous	59356830
2	207970759	207970760	C	CAAA	7	GENIC	heterozygous	59356831
2	207970999	207971000	C	A	32	GENIC	homozygous	59356832
2	207971244	207971245	C	T	44	GENIC	homozygous	59356833
2	207973017	207973018	T	C	23	GENIC	homozygous	59356834
2	207974874	207974875	T	C	15	GENIC	homozygous	59356835
2	207976322	207976338	CACGCACGCACGCACA	----------------	8	GENIC	homozygous	60585306
2	207977811	207977812	G	GT	25	GENIC	homozygous	59356838
2	207978277	207978279	GG	--	3	GENIC	heterozygous	59356840
2	207980587	207980588	A	G	41	GENIC	homozygous	59356842