chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	174766487	174766487		GG	20	GENIC	homozygous	127458057
1	174766738	174766739	C	T	44	GENIC	homozygous	108393009
1	174766843	174766845	AA		43	GENIC	homozygous	127458058
1	174766972	174766973	T	C	38	GENIC	homozygous	108393011
1	174767104	174767105	G	A	46	GENIC	homozygous	108393013
1	174767270	174767271	A	G	40	GENIC	homozygous	108393015
1	174767771	174767771		GCG	57	GENIC	homozygous	127458059
1	174768852	174768853	C	T	35	GENIC	homozygous	108393017
1	174775958	174775959	G	A	43	GENIC	homozygous	108961468
1	174779542	174779542		C	41	GENIC	homozygous	127458060
1	174779930	174779931	G	A	41	GENIC	homozygous	108393029
1	174780244	174780245	A	G	44	GENIC	homozygous	108393031
1	174781008	174781009	A	C	35	GENIC	homozygous	108393033
1	174781009	174781010	T	A	35	GENIC	homozygous	108393035
1	174781363	174781364	G	A	51	GENIC	homozygous	108393037
1	174781736	174781737	T	C	31	GENIC	homozygous	108393039
1	174787514	174787515	G	A	19	GENIC	possibly homozygous	108393043
1	174788601	174788602	A	G	41	GENIC	possibly homozygous	108393045
1	174784122	174784125	TTC		32	GENIC	homozygous	130827877