chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105568539	105568540	A	G	16	GENIC	homozygous	116837136
10	105568777	105568778	T	C	19	GENIC	homozygous	116837138
10	105569180	105569181	C	G	27	GENIC	homozygous	116837140
10	105569232	105569233	T	C	30	GENIC	homozygous	116837142
10	105569499	105569500	C	T	28	GENIC	homozygous	116837144
10	105569518	105569519	A	G	27	GENIC	homozygous	116837146
10	105569583	105569584	C	T	22	GENIC	homozygous	116837148
10	105569639	105569640	G	A	40	GENIC	homozygous	116837150
10	105569650	105569651	C	T	36	GENIC	homozygous	116837152
10	105569707	105569708	T	C	17	GENIC	homozygous	116837154
10	105570831	105570832	T	C	31	GENIC	homozygous	116837156
10	105571011	105571012	G	A	26	GENIC	homozygous	116837158
10	105571015	105571016	G	A	27	GENIC	homozygous	116837160
10	105572049	105572050	G	T	14	GENIC	homozygous	116837162
10	105572123	105572124	C	G	24	GENIC	homozygous	116837164
10	105572362	105572363	T	C	23	GENIC	homozygous	116837166