chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	100964900	100964901	T	G	33	GENIC	homozygous	51758929
10	100966938	100966939	G	-	14	GENIC	homozygous	51579786
10	100966942	100966943	T	TC	12	GENIC	homozygous	51579788
10	100966948	100966950	CC	--	10	GENIC	heterozygous	51998714
10	100966949	100966950	C	-	10	GENIC	possibly homozygous	51579790
10	100967120	100967121	G	A	35	GENIC	heterozygous	51758931
10	100967122	100967123	G	A	34	GENIC	possibly homozygous	51758933
10	100967124	100967125	G	A	33	GENIC	heterozygous	51758935
10	100967129	100967130	C	A	36	GENIC	heterozygous	51758937
10	100967888	100967889	G	T	42	GENIC	homozygous	51758939
10	100968421	100968422	C	CTTTT	6	GENIC	homozygous	51758941
10	100968504	100968505	C	CT	4	GENIC	heterozygous	51758943
10	100968863	100968864	T	TAA	6	GENIC	homozygous	51758945
10	100969183	100969184	G	A	10	GENIC	possibly homozygous	51758947
10	100969293	100969294	A	AAT	2	GENIC	homozygous	51758949
10	100969644	100969645	T	-	7	GENIC	homozygous	51758951
10	100969722	100969724	TT	--	8	GENIC	homozygous	51758953
10	100970163	100970164	T	C	28	GENIC	homozygous	51758955
10	100970263	100970264	C	CTT	5	GENIC	homozygous	51758957