chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	63676355	63676356	T	G	27	GENIC	homozygous	116616348
10	63677706	63677707	A	T	30	GENIC	homozygous	116940601
10	63682057	63682058	T	C	27	GENIC	homozygous	116616358
10	63683053	63683054	G	A	26	GENIC	homozygous	116940603
10	63684180	63684181	C	T	38	GENIC	possibly homozygous	116940605
10	63688048	63688049	C	T	31	GENIC	homozygous	116616362
10	63693199	63693200	C	T	26	GENIC	homozygous	116940607
10	63693832	63693833	G	T	30	GENIC	homozygous	116616370
10	63694171	63694172	A	T	19	GENIC	homozygous	116940609
10	63696396	63696397	C	T	35	GENIC	homozygous	116940611
10	63699131	63699132	A	G	22	GENIC	homozygous	116940613
10	63701842	63701843	T	G	19	GENIC	homozygous	116616380
10	63703298	63703299	T	C	31	GENIC	homozygous	116616392
10	63703678	63703679	A	G	36	GENIC	homozygous	116616396
10	63708630	63708631	C	T	25	GENIC	homozygous	116940615
10	63709869	63709870	A	G	25	GENIC	homozygous	116616418
10	63710942	63710943	A	T	37	GENIC	homozygous	116616424
10	63718730	63718731	A	T	25	GENIC	homozygous	116940617
10	63714081	63714082	A	T	21	GENIC	possibly homozygous	116978547