chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61624224	61624225	C	T	9	GENIC	homozygous	142253001
10	61642612	61642612		AT	7	GENIC	heterozygous	138686704
10	61658276	61658277	C	A	16	GENIC	homozygous	138802466
10	61663971	61663972	G	A	16	GENIC	homozygous	142253002
10	61680643	61680644	A		8	GENIC	heterozygous	403288314
10	61680638	61680639	A	G	6	GENIC	homozygous	403288307
10	61680638	61680639	A		6	GENIC	heterozygous	403288308
10	61680643	61680644	A	G	8	GENIC	possibly homozygous	403288313
10	61680644	61680645	A	G	8	GENIC	possibly homozygous	403288315
10	61680644	61680645	A		8	GENIC	heterozygous	403288316
10	61683971	61683972	C		7	GENIC	heterozygous	403288317
10	61683971	61683972	C	G	7	GENIC	heterozygous	403288318
10	61685262	61685263	C	T	21	GENIC	homozygous	142253003
10	61685286	61685287	C	T	20	GENIC	homozygous	142253004
10	61685651	61685652	G	A	21	GENIC	homozygous	138802494
10	61685831	61685831		TC	13	GENIC	homozygous	142204640
10	61686303	61686304	C	T	18	GENIC	homozygous	138802496
10	61686379	61686381	GC		21	GENIC	homozygous	142204641
10	61686505	61686506	T	G	24	GENIC	homozygous	138802497