chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	20343996	20343997	G	T	39	GENIC	possibly homozygous	139470690
14	20346106	20346107	A	G	35	GENIC	homozygous	144119289
14	20349866	20349867	G	C	40	GENIC	homozygous	139470691
14	20350080	20350081	G	A	47	GENIC	homozygous	139470693
14	20353315	20353316	G	T	32	GENIC	homozygous	139470694
14	20355174	20355175	C	T	30	GENIC	homozygous	139470695
14	20355315	20355316	G	A	51	GENIC	homozygous	144119290
14	20355613	20355617	ATGT		25	GENIC	homozygous	139383469
14	20355058	20355059	T		33	GENIC	possibly homozygous	139383468
14	20357116	20357117	C	T	33	GENIC	heterozygous	403354233
14	20357116	20357117	C		33	GENIC	homozygous	403354234
14	20357113	20357114	A		33	GENIC	homozygous	403354231
14	20357113	20357114	A	G	33	GENIC	heterozygous	403354232
14	20357129	20357130	A	G	22	GENIC	heterozygous	403354235
14	20357129	20357130	A		22	GENIC	heterozygous	403354236