chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	40450338	40450338		CAA	43	GENIC	homozygous	129355389
16	40460360	40460361	A	G	44	GENIC	heterozygous	119160021
16	40460381	40460382	G	T	45	GENIC	heterozygous	119160023
16	40460402	40460403	A	T	43	GENIC	heterozygous	119160025
16	40460409	40460410	A	C	39	GENIC	heterozygous	119160027
16	40483892	40483893	G	C	15	GENIC	heterozygous	131948029
16	40499963	40499964	C		52	GENIC	homozygous	129355396
16	40532332	40532333	T	G	2	GENIC	homozygous	131948030
16	40532342	40532343	A		3	GENIC	homozygous	129355399
16	40532358	40532360	TC		4	GENIC	homozygous	129355400
16	40532362	40532363	C	G	6	GENIC	homozygous	129406914
16	40532350	40532351	C	G	3	GENIC	homozygous	129406913
16	40532060	40532061	C		2	GENIC	homozygous	130453708
16	40532111	40532111		C	2	GENIC	homozygous	130453709
16	40532143	40532144	C		2	GENIC	homozygous	130453710
16	40532129	40532130	C	T	2	GENIC	homozygous	119219692
16	40532169	40532170	T	C	2	GENIC	homozygous	119219693
16	40532137	40532138	C	A	2	GENIC	homozygous	130459289
16	40532149	40532150	G	A	2	GENIC	homozygous	130459290
16	40532362	40532362		T	4	GENIC	homozygous	129355401
16	40532390	40532390		G	9	GENIC	homozygous	129355402
16	40532406	40532407	C	T	11	GENIC	homozygous	119114585
16	40532454	40532455	A		22	GENIC	homozygous	129355403
16	40539435	40539436	C	A	57	GENIC	homozygous	111974568