chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	30864346	30864347	A	G	44	GENIC	homozygous	111024017
17	30864802	30864803	G	C	42	GENIC	homozygous	111024019
17	30865352	30865353	A	C	48	GENIC	homozygous	111024021
17	30868308	30868309	A	G	38	GENIC	homozygous	111024023
17	30868082	30868083	T		25	GENIC	possibly homozygous	129442413
17	30868361	30868363	AT		42	GENIC	homozygous	129442414
17	30879322	30879323	A	C	45	GENIC	homozygous	111024025
17	30879330	30879331	T	G	45	GENIC	homozygous	111024027
17	30880020	30880021	T	C	42	GENIC	homozygous	111024029
17	30880082	30880083	T	C	45	GENIC	homozygous	111024031
17	30869845	30869846	C	T	18	GENIC	homozygous	119272649
17	30880152	30880153	C	T	48	GENIC	homozygous	111024033
17	30880738	30880739	T	C	42	GENIC	homozygous	111024035
17	30881463	30881464	C	A	50	GENIC	homozygous	111024037
17	30882069	30882070	T	C	36	GENIC	homozygous	111024039
17	30869621	30869622	A	G	41	GENIC	heterozygous	131753551
17	30869625	30869626	G	A	43	GENIC	heterozygous	131753552