chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	141004120	141004121	A	G	41	GENIC	homozygous	143029358
3	141005616	141005617	A	G	56	GENIC	homozygous	143029359
3	141006007	141006008	G	A	57	GENIC	possibly homozygous	143029360
3	141006222	141006223	G	A	54	GENIC	homozygous	143029361
3	141006361	141006362	G	C	52	GENIC	possibly homozygous	143029362
3	141006531	141006532	G	A	56	GENIC	homozygous	143029363
3	141006743	141006744	A	G	47	GENIC	homozygous	143029364
3	141007085	141007086	T	C	52	GENIC	homozygous	143029365
3	141007193	141007193		T	42	GENIC	homozygous	143002659
3	141007911	141007927	CCCAAAGGGATTGTGA		49	GENIC	possibly homozygous	143002660
3	141008250	141008251	T	C	31	GENIC	homozygous	143029366
3	141008721	141008722	G	A	24	GENIC	homozygous	143029367
3	141008763	141008764	T	C	27	GENIC	homozygous	143029368
3	141008865	141008866	T	G	34	GENIC	homozygous	143029369
3	141008878	141008879	A	G	31	GENIC	homozygous	143029370
3	141008950	141008951	A	G	48	GENIC	homozygous	143029371
3	141008974	141008975	T	C	51	GENIC	homozygous	143029372
3	141009061	141009062	T	C	55	GENIC	homozygous	143029373