chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	110669704	110669705	T	C	22	GENIC	homozygous	112003935
3	110669764	110669765	A	G	30	GENIC	homozygous	112003937
3	110670472	110670473	C	T	23	GENIC	homozygous	112139000
3	110671832	110671833	G	A	23	GENIC	homozygous	112003939
3	110672711	110672712	G	C	28	GENIC	homozygous	112003943
3	110673349	110673350	T	A	21	GENIC	homozygous	111673167
3	110674207	110674208	T	C	22	GENIC	homozygous	112139001
3	110674208	110674209	G	A	22	GENIC	homozygous	112139002
3	110674465	110674466	T	C	16	GENIC	homozygous	111673170
3	110674854	110674855	A	G	27	GENIC	homozygous	111673172
3	110676197	110676198	G	T	21	GENIC	homozygous	111673173
3	110676200	110676201	T	A	21	GENIC	homozygous	111673175
3	110676206	110676207	G	T	20	GENIC	possibly homozygous	111673177
3	110679217	110679218	C	T	23	GENIC	homozygous	111673183
3	110684387	110684388	A	C	20	GENIC	homozygous	111673190
3	110684444	110684445	C	T	23	GENIC	homozygous	112139003