chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61624224	61624225	C	T	36	GENIC	homozygous	142253001
10	61642612	61642612		AT	34	GENIC	possibly homozygous	138686704
10	61658276	61658277	C	A	58	GENIC	homozygous	138802466
10	61663971	61663972	G	A	34	GENIC	homozygous	142253002
10	61671530	61671531	C		6	GENIC	homozygous	142204639
10	61680641	61680642	A	G	5	GENIC	heterozygous	403288310
10	61680641	61680642	A		5	GENIC	heterozygous	403288309
10	61671555	61671556	G		7	GENIC	possibly homozygous	403288305
10	61671555	61671556	G	T	7	GENIC	heterozygous	403288306
10	61680642	61680643	A		6	GENIC	heterozygous	403288311
10	61680642	61680643	A	G	6	GENIC	heterozygous	403288312
10	61685262	61685263	C	T	51	GENIC	homozygous	142253003
10	61685286	61685287	C	T	53	GENIC	homozygous	142253004
10	61685651	61685652	G	A	44	GENIC	homozygous	138802494
10	61685831	61685831		TC	57	GENIC	homozygous	142204640
10	61686303	61686304	C	T	36	GENIC	homozygous	138802496
10	61686379	61686381	GC		36	GENIC	homozygous	142204641
10	61686505	61686506	T	G	41	GENIC	homozygous	138802497