chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105568153	105568154	A	G	31	GENIC	homozygous	116837132
10	105568214	105568215	A	T	23	GENIC	homozygous	116837134
10	105568539	105568540	A	G	40	GENIC	homozygous	116837136
10	105568777	105568778	T	C	33	GENIC	homozygous	116837138
10	105569180	105569181	C	G	39	GENIC	homozygous	116837140
10	105569232	105569233	T	C	43	GENIC	homozygous	116837142
10	105569499	105569500	C	T	43	GENIC	homozygous	116837144
10	105569518	105569519	A	G	43	GENIC	homozygous	116837146
10	105569583	105569584	C	T	42	GENIC	homozygous	116837148
10	105569639	105569640	G	A	33	GENIC	homozygous	116837150
10	105569650	105569651	C	T	36	GENIC	homozygous	116837152
10	105569707	105569708	T	C	31	GENIC	homozygous	116837154
10	105570102	105570102		ATAT	10	GENIC	homozygous	133233631
10	105570119	105570120	G		5	GENIC	homozygous	133233632
10	105570121	105570154	TGCACACACACAGATACACACACACAGAGATGC		4	GENIC	homozygous	133233633
10	105570164	105570166	AC		5	GENIC	homozygous	133233634
10	105570176	105570178	AC		5	GENIC	homozygous	133233635
10	105570192	105570202	ACACACATAT		5	GENIC	homozygous	133233636
10	105570223	105570224	T	G	5	GENIC	homozygous	126489858
10	105570831	105570832	T	C	38	GENIC	homozygous	116837156
10	105571011	105571012	G	A	38	GENIC	homozygous	116837158
10	105571015	105571016	G	A	39	GENIC	homozygous	116837160
10	105572049	105572050	G	T	47	GENIC	possibly homozygous	116837162
10	105572123	105572124	C	G	55	GENIC	possibly homozygous	116837164
10	105572362	105572363	T	C	48	GENIC	homozygous	116837166