chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	10160705	10160706	T	C	57	GENIC	homozygous	117244133
9	10160907	10160908	G	T	47	GENIC	homozygous	117244134
9	10162485	10162486	T	C	50	GENIC	homozygous	117244135
9	10162506	10162507	G	A	47	GENIC	homozygous	117244136
9	10162761	10162762	T	C	61	GENIC	homozygous	117244137
9	10163136	10163137	C	T	53	GENIC	homozygous	117244138
9	10163346	10163347	G	A	44	GENIC	homozygous	117244139
9	10163412	10163413	G	T	41	GENIC	homozygous	117244140
9	10163563	10163564	T	C	26	GENIC	homozygous	117244141
9	10165105	10165106	C	T	46	GENIC	homozygous	117244142
9	10165876	10165877	C	T	54	GENIC	homozygous	117244143
9	10169070	10169071	G	A	49	GENIC	homozygous	117244145
9	10170201	10170202	C	T	35	GENIC	homozygous	117244146
9	10171475	10171476	G	A	30	GENIC	homozygous	117244147
9	10171539	10171540	T	A	26	GENIC	homozygous	117244148
9	10172228	10172229	T	C	42	GENIC	homozygous	117244149
9	10174810	10174811	T	C	40	GENIC	possibly homozygous	117244151
9	10175917	10175918	A	G	38	GENIC	homozygous	117244155
9	10176926	10176927	T	C	25	GENIC	homozygous	117244156
9	10181131	10181132	G	A	34	GENIC	homozygous	117244157
9	10181781	10181782	T	C	59	GENIC	homozygous	117244158
9	10184126	10184127	T	C	44	GENIC	homozygous	117244160
9	10185446	10185447	C	T	35	GENIC	homozygous	117244161
9	10186277	10186278	G	A	20	GENIC	homozygous	117244162