chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	122194745	122194746	C	T	25	GENIC	homozygous	111690175
3	122195519	122195520	A	G	34	GENIC	homozygous	111690176
3	122195581	122195582	C	T	27	GENIC	homozygous	119879569
3	122195603	122195604	A	G	26	GENIC	homozygous	111690177
3	122196249	122196250	T	G	25	GENIC	homozygous	111690178
3	122197178	122197179	G	A	22	GENIC	homozygous	111690180
3	122197578	122197579	T	C	29	GENIC	homozygous	111690181
3	122197583	122197584	T	C	27	GENIC	homozygous	111690182
3	122198210	122198211	G	A	26	GENIC	homozygous	111690183
3	122198281	122198282	A	G	25	GENIC	homozygous	111690184
3	122201835	122201836	A	G	27	GENIC	homozygous	111690186
3	122202472	122202473	A	C	24	GENIC	homozygous	119879570
3	122202770	122202771	T	C	27	GENIC	homozygous	111690187
3	122204217	122204218	G	A	37	GENIC	homozygous	119879571
3	122205159	122205160	C	G	26	GENIC	homozygous	111690190
3	122205431	122205432	G	T	16	GENIC	homozygous	119879572
3	122205452	122205453	A	G	17	GENIC	homozygous	111690191
3	122205933	122205934	C	G	28	GENIC	homozygous	111690192
3	122206279	122206280	A	G	18	GENIC	homozygous	111690193