chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	5973361	5973362	A	T	33	GENIC	homozygous	403845128
12	5974127	5974128	C	G	21	GENIC	homozygous	146253231
12	5974801	5974802	A	T	39	GENIC	homozygous	139072188
12	5974139	5974139		CTC	20	GENIC	homozygous	139037971
12	5974698	5974699	T		38	GENIC	possibly homozygous	139037972
12	5974867	5974867		TTG	29	GENIC	homozygous	139037973
12	5975372	5975373	C	T	50	GENIC	homozygous	139072190
12	5974535	5974536	C	A	41	GENIC	homozygous	139072187
12	5975015	5975016	C	T	51	GENIC	homozygous	139072189
12	5976513	5976515	AT		45	GENIC	homozygous	139037974
12	5976617	5976618	T	C	50	GENIC	homozygous	139072191
12	5976728	5976729	G	T	53	GENIC	homozygous	139072192
12	5976989	5976990	G	A	36	GENIC	homozygous	139072193
12	5978349	5978349		TT	20	GENIC	homozygous	139037975