chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	122311130	122311131	C	A	38	GENIC	homozygous	112357260
3	122311869	122311870	T	G	33	GENIC	homozygous	111690405
3	122312046	122312047	G	A	27	GENIC	homozygous	112357262
3	122312911	122312912	G	A	16	GENIC	homozygous	112357264
3	122316010	122316011	C	T	32	GENIC	homozygous	111690408
3	122317053	122317054	G	A	31	GENIC	homozygous	112147036
3	122317140	122317141	A	G	26	GENIC	homozygous	111690409
3	122317427	122317428	C	G	31	GENIC	homozygous	112357266
3	122317589	122317590	A	G	33	GENIC	homozygous	111690411
3	122317739	122317740	G	A	28	GENIC	homozygous	111690412
3	122317754	122317755	G	C	34	GENIC	homozygous	111690413
3	122318282	122318283	T	C	46	GENIC	homozygous	111690414
3	122319048	122319049	G	T	28	GENIC	heterozygous	111690418
3	122319256	122319257	G	A	27	GENIC	homozygous	111690419
3	122320240	122320241	T	C	28	GENIC	homozygous	111690421
3	122320558	122320559	G	A	23	GENIC	homozygous	112357268
3	122321301	122321302	T	C	43	GENIC	homozygous	111690424
3	122323532	122323533	T	C	29	GENIC	homozygous	111690426
3	122325956	122325957	C	G	31	GENIC	homozygous	112357270
3	122326162	122326163	T	A	22	GENIC	homozygous	112357272
3	122326308	122326309	G	A	23	GENIC	homozygous	111690435
3	122327696	122327697	C	A	17	GENIC	homozygous	112357274
3	122332557	122332558	G	T	40	GENIC	homozygous	112357276
3	122336144	122336145	T	C	27	GENIC	homozygous	111690449
3	122339709	122339710	A	G	17	GENIC	homozygous	111690453