chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	171296761	171296762	C	T	33	GENIC	possibly homozygous	112206131
3	171298431	171298432	G	C	41	GENIC	homozygous	112206133
3	171298560	171298561	A	G	28	GENIC	homozygous	112206135
3	171298567	171298568	G	A	28	GENIC	homozygous	112206137
3	171298663	171298664	C	T	20	GENIC	homozygous	112206139
3	171299049	171299050	G	T	46	GENIC	homozygous	112206141
3	171300896	171300897	G	A	26	GENIC	homozygous	112206143
3	171300939	171300940	T	C	17	GENIC	heterozygous	112206149
3	171301213	171301214	A	C	20	GENIC	possibly homozygous	112258386
3	171301259	171301260	G	A	21	GENIC	homozygous	112206153
3	171301765	171301766	T	C	31	GENIC	homozygous	112206155
3	171302170	171302171	T	C	27	GENIC	homozygous	112206157
3	171302654	171302655	G	A	30	GENIC	homozygous	112206159
3	171303043	171303044	A	T	20	GENIC	heterozygous	112258387
3	171303214	171303215	C	A	25	GENIC	homozygous	112206160
3	171304031	171304032	C	T	23	GENIC	homozygous	112206161
3	171304038	171304039	T	G	23	GENIC	homozygous	112206162
3	171304169	171304170	C	T	26	GENIC	homozygous	112206163
3	171304234	171304235	A	G	26	GENIC	homozygous	112206164
3	171304971	171304972	C	T	37	GENIC	homozygous	112206165
3	171305144	171305145	C	A	47	GENIC	homozygous	112206166
3	171306164	171306165	G	T	34	GENIC	possibly homozygous	112206167
3	171306364	171306365	C	T	25	GENIC	homozygous	112206168
3	171306431	171306432	T	C	37	GENIC	homozygous	112206169
3	171308286	171308287	G	A	38	GENIC	homozygous	112206170
3	171308846	171308847	T	C	41	GENIC	homozygous	112206171
3	171309165	171309166	G	A	46	GENIC	homozygous	112206172
3	171309573	171309574	A	G	38	GENIC	homozygous	112206173
3	171311119	171311120	G	A	32	GENIC	homozygous	112206174
3	171303057	171303058	G	C	28	GENIC	heterozygous	111836858
3	171303061	171303062	C	T	24	GENIC	heterozygous	111836860