chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	109816430	109816431	G	C	27	GENIC	homozygous	141529363
3	109818826	109818827	C	T	17	GENIC	homozygous	141529364
3	109820292	109820293	C	T	19	GENIC	homozygous	141529365
3	109820884	109820885	C	T	20	GENIC	homozygous	141529366
3	109818972	109818974	TG		21	GENIC	homozygous	136583637
3	109823498	109823499	A	G	13	GENIC	possibly homozygous	141529367
3	109823502	109823503	A	G	13	GENIC	possibly homozygous	141529368
3	109823645	109823646	T	C	20	GENIC	homozygous	141529369
3	109824586	109824587	T	C	19	GENIC	homozygous	141529370
3	109823494	109823495	A		13	GENIC	heterozygous	403073989
3	109823494	109823495	A	G	13	GENIC	possibly homozygous	154110720
3	109824137	109824138	G	A	10	GENIC	heterozygous	154110722
3	109824137	109824138	G		10	GENIC	heterozygous	403073990
3	109824139	109824140	G		10	GENIC	heterozygous	403073991
3	109824139	109824140	G	A	10	GENIC	heterozygous	403073992
3	109824084	109824094	TCTCTGTCTC		22	GENIC	homozygous	141479408
3	109824979	109824980	A	G	12	GENIC	homozygous	141529371