chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	30468831	30468832	T	C	20	GENIC	homozygous	111022351
17	30469024	30469025	G	A	14	GENIC	homozygous	111022355
17	30469254	30469255	G	T	31	GENIC	homozygous	111022357
17	30469311	30469312	G	C	32	GENIC	homozygous	111022359
17	30469515	30469516	T	C	21	GENIC	homozygous	111241707
17	30469687	30469688	A	G	14	GENIC	homozygous	111241709
17	30469939	30469940	C	A	19	GENIC	homozygous	111241711
17	30470016	30470017	A	C	14	GENIC	homozygous	111241713
17	30470172	30470173	T	G	25	GENIC	homozygous	111022361
17	30470199	30470200	T	G	27	GENIC	homozygous	111241715
17	30470301	30470302	C	T	38	GENIC	homozygous	111022367
17	30470309	30470310	G	C	38	GENIC	homozygous	111241716
17	30470358	30470359	T	C	37	GENIC	homozygous	111022369
17	30470386	30470387	G	A	43	GENIC	heterozygous	119360521
17	30470404	30470405	G	A	44	GENIC	heterozygous	119415663
17	30470413	30470414	G	A	42	GENIC	heterozygous	119446733
17	30470645	30470646	T	C	56	GENIC	possibly homozygous	111022371
17	30472448	30472449	T	C	36	GENIC	homozygous	111022373
17	30473239	30473240	G	A	23	GENIC	homozygous	111241718
17	30474078	30474079	T	C	15	GENIC	homozygous	111022375