chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12710052	12710053	A	G	35	GENIC	homozygous	116316819
7	12710596	12710597	C	T	33	GENIC	homozygous	116316821
7	12710763	12710764	T	C	22	GENIC	homozygous	116316823
7	12711086	12711087	T	C	20	GENIC	homozygous	116316825
7	12711699	12711700	T	G	29	GENIC	possibly homozygous	116316827
7	12712205	12712206	G	A	32	GENIC	homozygous	116316829
7	12712913	12712914	C	G	20	GENIC	homozygous	116316831
7	12713555	12713556	T	G	25	GENIC	homozygous	116316833
7	12713649	12713650	C	G	19	GENIC	homozygous	116316835
7	12714700	12714701	T	C	17	GENIC	homozygous	116316841
7	12714901	12714902	T	C	12	GENIC	homozygous	116316845
7	12715145	12715146	T	A	4	GENIC	homozygous	116316847
7	12716014	12716015	A	G	27	GENIC	homozygous	116316855
7	12716629	12716630	C	T	29	GENIC	homozygous	116316857
7	12716804	12716805	T	C	25	GENIC	homozygous	115570387
7	12718288	12718289	T	C	18	GENIC	homozygous	115570390
7	12719449	12719450	A	G	22	GENIC	homozygous	115570403
7	12719647	12719648	G	A	23	GENIC	homozygous	116274957