chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	15332164	15332165	T	TTCC	21	GENIC	possibly homozygous	51331047
10	15333933	15333935	AA	--	7	GENIC	heterozygous	51331048
10	15333934	15333935	A	-	7	GENIC	heterozygous	51331049
10	15335560	15335561	A	G	42	GENIC	homozygous	51331050
10	15339277	15339278	C	T	33	GENIC	homozygous	51331051
10	15339863	15339864	C	CT	2	GENIC	heterozygous	51331052
10	15339863	15339864	C	CTT	2	GENIC	heterozygous	51331053
10	15346957	15346958	T	C	13	GENIC	homozygous	51331054
10	15350398	15350399	G	GT	15	GENIC	possibly homozygous	51331055
10	15352206	15352207	C	CT	19	GENIC	heterozygous	51624614
10	15352207	15352208	T	-	19	GENIC	heterozygous	51624615
10	15353853	15353854	T	TA	9	GENIC	possibly homozygous	51331056
10	15354661	15354662	G	GA	14	GENIC	possibly homozygous	51331057
10	15354684	15354685	A	AG	10	GENIC	heterozygous	51331059
10	15354684	15354685	A	AAG	10	GENIC	heterozygous	51331060
10	15355413	15355414	T	TC	17	GENIC	possibly homozygous	51812337
10	15358044	15358052	ATACATAC	--------	8	GENIC	heterozygous	51331061
10	15362111	15362112	A	AG	19	GENIC	homozygous	51331064
10	15362376	15362377	G	GCAT	43	GENIC	homozygous	51331065
10	15362679	15362683	AAAC	----	17	GENIC	homozygous	51331067
10	15365434	15365435	G	A	21	GENIC	heterozygous	51982719
10	15366811	15366812	A	-	3	GENIC	heterozygous	51624630
10	15368571	15368572	T	TAC	12	GENIC	homozygous	51331068