chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61684197	61684198	G	A	13	GENIC	homozygous	116939439
10	61684886	61684887	T	C	20	GENIC	homozygous	116612998
10	61685807	61685808	C	T	26	GENIC	homozygous	116613000
10	61685815	61685816	T	C	22	GENIC	homozygous	116613002
10	61687164	61687165	C	T	19	GENIC	homozygous	116939441
10	61687165	61687166	C	T	20	GENIC	homozygous	116939443
10	61691766	61691767	C	G	17	GENIC	homozygous	116939445
10	61693994	61693995	A	G	19	GENIC	homozygous	116613008
10	61694412	61694413	T	C	14	GENIC	homozygous	117997247
10	61687660	61687661	C	G	22	GENIC	homozygous	116790683
10	61688120	61688120		TTTTAAC	23	GENIC	homozygous	128822366
10	61692739	61692741	CT		16	GENIC	homozygous	128822367
10	61688554	61688559	TGACT		27	GENIC	homozygous	131095380