chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	73938951	73938952	T	A	36	GENIC	homozygous	117376802
9	73939516	73939517	C	T	35	GENIC	homozygous	117559324
9	73940371	73940372	A	C	28	GENIC	homozygous	117559326
9	73940821	73940822	C	T	23	GENIC	homozygous	117376803
9	73942265	73942266	T	A	20	GENIC	homozygous	117559328
9	73942319	73942320	G	A	18	GENIC	homozygous	117559330
9	73942691	73942692	T	C	23	GENIC	homozygous	117376805
9	73943036	73943037	A	G	18	GENIC	homozygous	117376806
9	73943639	73943640	G	C	41	GENIC	homozygous	117376809
9	73943835	73943836	C	T	24	GENIC	homozygous	117376810
9	73944350	73944351	T	C	14	GENIC	homozygous	117376811
9	73946281	73946282	A	G	28	GENIC	homozygous	117559332
9	73946352	73946353	G	A	20	GENIC	homozygous	117376813
9	73949230	73949231	C	T	32	GENIC	homozygous	117559334
9	73950208	73950209	T	C	17	GENIC	homozygous	117559336
9	73950721	73950722	A	G	28	GENIC	homozygous	117376815
9	73951059	73951060	C	A	27	GENIC	homozygous	117559338
9	73952385	73952386	G	A	19	GENIC	homozygous	117559340
9	73957148	73957149	T	C	29	GENIC	homozygous	117376822