chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	39565384	39565385	T	C	9	GENIC	homozygous	138771180
10	39565608	39565609	C	T	19	GENIC	homozygous	138771181
10	39566122	39566123	G	C	31	GENIC	homozygous	138771182
10	39567095	39567096	G	A	16	GENIC	homozygous	138771183
10	39568198	39568199	A	G	17	GENIC	homozygous	138771184
10	39569673	39569678	TCTGT		11	GENIC	homozygous	138679864
10	39571177	39571178	A	C	22	GENIC	homozygous	138771185
10	39573059	39573060	A	C	21	GENIC	homozygous	138771186
10	39574800	39574801	C	T	21	GENIC	homozygous	138771187
10	39575176	39575177	C	T	20	GENIC	homozygous	138771188
10	39575650	39575651	A	T	24	GENIC	homozygous	138771189
10	39576096	39576097	T	C	26	GENIC	homozygous	138771190
10	39576475	39576476	C	T	18	GENIC	homozygous	138771191
10	39577231	39577232	A	G	21	GENIC	homozygous	138771192
10	39577619	39577620	C	T	16	GENIC	homozygous	138771193
10	39576903	39576904	A		15	GENIC	homozygous	403633569
10	39576903	39576904	A	G	15	GENIC	heterozygous	403633570