chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13548029	13548030	C	T	13	GENIC	heterozygous	51621451
10	13548047	13548048	G	A	14	GENIC	heterozygous	51621452
10	13548064	13548065	A	G	15	GENIC	heterozygous	51621453
10	13553097	13553098	G	A	22	GENIC	heterozygous	51621519
10	13553229	13553230	C	T	22	GENIC	heterozygous	51621520
10	13553235	13553236	T	C	24	GENIC	heterozygous	51621521
10	13553422	13553423	G	A	7	GENIC	heterozygous	51621522
10	13554527	13554528	C	T	13	GENIC	heterozygous	51621535
10	13554625	13554626	G	T	37	GENIC	heterozygous	51621536
10	13554652	13554653	G	A	50	GENIC	heterozygous	51621537
10	13554674	13554675	A	G	60	GENIC	heterozygous	51621538
10	13554788	13554789	C	T	38	GENIC	heterozygous	51621539
10	13554945	13554946	T	A	15	GENIC	heterozygous	51621540
10	13555506	13555507	C	T	16	GENIC	heterozygous	51621547
10	13555562	13555563	G	T	24	GENIC	heterozygous	51621548
10	13572430	13572431	G	A	27	GENIC	heterozygous	51621649
10	13575049	13575050	T	C	15	GENIC	heterozygous	51621652
10	13586289	13586290	G	A	9	GENIC	heterozygous	51621679
10	13588297	13588298	C	T	16	GENIC	heterozygous	51621685
10	13588493	13588494	G	A	13	GENIC	heterozygous	51621686
10	13588750	13588751	A	G	23	GENIC	heterozygous	51621687
10	13592773	13592774	A	G	13	GENIC	heterozygous	51621701
10	13596686	13596687	T	C	13	GENIC	heterozygous	51621710