chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109389134	109389135	C	T	34	GENIC	homozygous	51599138
10	109391046	109391047	T	C	32	GENIC	homozygous	51599139
10	109391914	109391915	G	A	26	GENIC	homozygous	51599140
10	109392071	109392073	CA	--	11	GENIC	homozygous	51599142
10	109392097	109392098	C	T	9	GENIC	homozygous	51599143
10	109393080	109393081	T	-	19	GENIC	possibly homozygous	51599150
10	109393643	109393645	TT	--	30	GENIC	homozygous	51599151
10	109393846	109393847	T	C	19	GENIC	homozygous	51599152
10	109394076	109394077	G	A	23	GENIC	homozygous	51599153
10	109394100	109394101	C	CT	16	GENIC	heterozygous	51599154
10	109394100	109394101	C	CTT	16	GENIC	possibly homozygous	51599155
10	109394149	109394150	A	AT	17	GENIC	homozygous	51599156
10	109394629	109394630	C	T	32	GENIC	homozygous	51599157
10	109394684	109394685	C	CTTTTTT	2	GENIC	homozygous	52734672
10	109394854	109394855	T	C	23	GENIC	homozygous	51599160
10	109394981	109394982	T	C	20	GENIC	homozygous	51599161