chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	73938440	73938441	A	T	20	GENIC	homozygous	117376800
9	73938628	73938629	A	T	23	GENIC	homozygous	117376801
9	73938951	73938952	T	A	44	GENIC	homozygous	117376802
9	73940821	73940822	C	T	56	GENIC	homozygous	117376803
9	73942265	73942266	T	A	44	GENIC	possibly homozygous	117559328
9	73942319	73942320	G	A	45	GENIC	homozygous	117559330
9	73940371	73940372	A	C	67	GENIC	homozygous	117559326
9	73942377	73942378	A	T	55	GENIC	homozygous	117744109
9	73942691	73942692	T	C	68	GENIC	homozygous	117376805
9	73943036	73943037	A	G	37	GENIC	homozygous	117376806
9	73943639	73943640	G	C	46	GENIC	homozygous	117376809
9	73943835	73943836	C	T	37	GENIC	homozygous	117376810
9	73944350	73944351	T	C	51	GENIC	homozygous	117376811
9	73946352	73946353	G	A	65	GENIC	possibly homozygous	117376813
9	73950721	73950722	A	G	41	GENIC	possibly homozygous	117376815
9	73953714	73953715	G	T	46	GENIC	possibly homozygous	117376816
9	73954263	73954264	C	A	39	GENIC	possibly homozygous	117376818
9	73950803	73950804	G	A	50	GENIC	possibly homozygous	120278691
9	73954613	73954614	C	G	47	GENIC	possibly homozygous	120278692
9	73954951	73954952	G	A	49	GENIC	homozygous	120278693
9	73956933	73956934	A	G	37	GENIC	homozygous	117376821
9	73956936	73956937	C	T	36	GENIC	homozygous	120278694
9	73957148	73957149	T	C	52	GENIC	homozygous	117376822
9	73957808	73957809	G	T	33	GENIC	homozygous	120278695
9	73957943	73957944	G	A	34	GENIC	homozygous	120278696