chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	27121301	27121302	T	C	17	GENIC	homozygous	111012347
17	27126421	27126422	T	C	16	GENIC	homozygous	125505061
17	27126791	27126792	G	A	24	GENIC	homozygous	111012349
17	27128048	27128049	G	A	17	GENIC	homozygous	111012351
17	27128286	27128287	A	G	9	GENIC	homozygous	111012353
17	27129683	27129684	T	C	8	GENIC	homozygous	125505062
17	27131932	27131933	T	C	9	GENIC	homozygous	111012355
17	27132295	27132296	A	G	19	GENIC	homozygous	111012357
17	27132729	27132730	C	T	29	GENIC	homozygous	111012359
17	27133038	27133039	T	C	12	GENIC	homozygous	111012361
17	27133651	27133652	A	T	16	GENIC	homozygous	111012363
17	27135033	27135034	T	C	8	GENIC	heterozygous	119271441
17	27135669	27135670	G	A	19	GENIC	homozygous	111012365
17	27138292	27138293	T	C	13	GENIC	homozygous	111012367
17	27138684	27138685	A	T	14	GENIC	homozygous	111012369
17	27140087	27140088	A	G	19	GENIC	homozygous	111012372
17	27141418	27141419	T	G	14	GENIC	homozygous	111012374
17	27145006	27145007	G	A	19	GENIC	homozygous	111012376
17	27146511	27146512	T	A	26	GENIC	possibly homozygous	111012378
17	27133479	27133480	G	A	12	GENIC	heterozygous	111398900
17	27139126	27139127	G	A	6	GENIC	homozygous	111402261