chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	19097411	19097412	G	A	25	GENIC	homozygous	111945933
16	19097798	19097799	C	T	26	GENIC	homozygous	111945935
16	19098175	19098176	G	T	37	GENIC	homozygous	111945937
16	19099303	19099304	T	A	16	GENIC	homozygous	111945939
16	19099559	19099560	A	G	24	GENIC	homozygous	111750644
16	19099772	19099773	T	C	21	GENIC	homozygous	111945941
16	19099833	19099834	T	C	33	GENIC	homozygous	111945943
16	19100036	19100037	A	G	27	GENIC	homozygous	112129083
16	19100080	19100081	C	T	20	GENIC	homozygous	111945947
16	19100081	19100082	A	G	20	GENIC	homozygous	111750646
16	19101568	19101569	G	A	31	GENIC	homozygous	112129087
16	19101845	19101846	T	C	27	GENIC	homozygous	111750650
16	19102550	19102551	T	G	26	GENIC	homozygous	112129089
16	19103440	19103441	C	A	20	GENIC	homozygous	111750652
16	19104781	19104782	T	C	27	GENIC	homozygous	111750654
16	19106221	19106222	G	A	13	GENIC	homozygous	112129091
16	19106226	19106227	G	A	13	GENIC	homozygous	112129093
16	19106928	19106929	G	A	28	GENIC	homozygous	112129095
16	19107918	19107919	C	T	20	GENIC	homozygous	112129097
16	19115474	19115475	T	C	26	GENIC	homozygous	111750660
16	19119868	19119869	T	C	21	GENIC	homozygous	111750672
16	19124004	19124005	G	C	9	GENIC	homozygous	112129099