chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	100964900	100964901	T	G	38	GENIC	homozygous	51758929
10	100966938	100966939	G	-	17	GENIC	homozygous	51579786
10	100966942	100966943	T	TC	16	GENIC	homozygous	51579788
10	100966948	100966950	CC	--	7	GENIC	heterozygous	51998714
10	100966949	100966950	C	-	7	GENIC	possibly homozygous	51579790
10	100967888	100967889	G	T	13	GENIC	homozygous	51758939
10	100968421	100968422	C	CTTTT	11	GENIC	possibly homozygous	51758941
10	100968504	100968505	C	CT	27	GENIC	heterozygous	51758943
10	100968863	100968864	T	TAA	37	GENIC	homozygous	51758945
10	100969183	100969184	G	A	27	GENIC	heterozygous	51758947
10	100969293	100969294	A	AAT	38	GENIC	homozygous	51758949
10	100969644	100969645	T	-	37	GENIC	homozygous	51758951
10	100969722	100969724	TT	--	43	GENIC	homozygous	51758953
10	100970163	100970164	T	C	31	GENIC	homozygous	51758955
10	100970263	100970264	C	CTT	29	GENIC	homozygous	51758957