chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51597827	51597828	C	A	13	GENIC	homozygous	114550001
13	51629251	51629252	T	C	8	GENIC	homozygous	114550002
13	51629252	51629253	G	T	8	GENIC	homozygous	114550003
13	51632780	51632781	A	G	8	GENIC	homozygous	114550004
13	51632828	51632829	G	T	7	GENIC	homozygous	114550005
13	51632832	51632833	C	A	5	GENIC	homozygous	114550006
13	51633512	51633513	G	T	8	GENIC	homozygous	114343713
13	51655368	51655369	G	T	8	GENIC	homozygous	114343820
13	51655375	51655376	G	C	8	GENIC	homozygous	114343822
13	51655391	51655392	G	A	8	GENIC	homozygous	114343824
13	51632886	51632887	A	G	6	GENIC	homozygous	114550007
13	51633547	51633548	T	C	5	GENIC	homozygous	114550008
13	51633549	51633550	A	T	5	GENIC	homozygous	114550009
13	51672816	51672817	G	C	7	GENIC	homozygous	114550010
13	51672854	51672855	T	A	5	GENIC	homozygous	114343866
13	51672858	51672859	A	C	5	GENIC	homozygous	114343868
13	51696535	51696536	C	T	15	GENIC	homozygous	114343900
13	51696536	51696537	A	C	15	GENIC	homozygous	114343902
13	51699743	51699744	C	T	12	GENIC	homozygous	114343908