chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	37324846	37324847	A	G	23	GENIC	homozygous	51416659
10	37325556	37325557	G	A	10	GENIC	homozygous	51416661
10	37325800	37325801	G	A	5	GENIC	homozygous	51416663
10	37326003	37326004	T	TG	3	GENIC	heterozygous	51416665
10	37326006	37326011	TTTTT	-----	6	GENIC	heterozygous	52493818
10	37326433	37326434	C	CTAGGCTG	20	GENIC	homozygous	51416669
10	37327778	37327779	A	T	18	GENIC	homozygous	51416671
10	37328710	37328721	TGCATGTAGAT	-----------	7	GENIC	homozygous	51416675
10	37328838	37328839	A	G	5	GENIC	homozygous	51416677
10	37328979	37328980	A	AT	13	GENIC	homozygous	51416679
10	37332205	37332206	G	GTGTT	15	GENIC	homozygous	51416681
10	37332798	37332799	A	C	22	GENIC	homozygous	51416683
10	37333162	37333182	ACAAACAAACAAACAAACAT	--------------------	3	GENIC	heterozygous	51416685
10	37334089	37334090	T	G	1	GENIC	homozygous	51416687
10	37334111	37334112	G	GTTTT	1	GENIC	homozygous	52681826
10	37334143	37334144	T	-	1	GENIC	homozygous	51416691
10	37333819	37333820	T	-	6	GENIC	heterozygous	51634490
10	37334122	37334123	G	GTTTGTT	1	GENIC	homozygous	52436021
10	37337098	37337106	TTTTTTTG	--------	9	GENIC	possibly homozygous	51416693
10	37337130	37337131	G	-	9	GENIC	homozygous	51416697
10	37338758	37338759	C	CT	13	GENIC	homozygous	51416699
10	37342127	37342128	C	T	14	GENIC	homozygous	51416701
10	37342829	37342830	A	-	16	GENIC	possibly homozygous	51634492
10	37337686	37337687	T	-	23	GENIC	heterozygous	51849252