chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	266845636	266845637	C	T	30	GENIC	homozygous	108638680
1	266845640	266845641	G	A	32	GENIC	homozygous	108638681
1	266846660	266846661	C	T	19	GENIC	homozygous	108638682
1	266847220	266847221	C	A	31	GENIC	homozygous	108638683
1	266847339	266847340	C	A	21	GENIC	homozygous	108638685
1	266847359	266847360	C	A	26	GENIC	homozygous	108638686
1	266848538	266848539	T	C	50	GENIC	homozygous	108638687
1	266849700	266849701	T	C	49	GENIC	homozygous	108638688
1	266850266	266850267	G	A	21	GENIC	homozygous	108638690
1	266850741	266850742	A	G	24	GENIC	homozygous	108638691
1	266851391	266851392	C	T	48	GENIC	homozygous	108638692
1	266851543	266851544	A	C	44	GENIC	homozygous	108638693
1	266851942	266851943	A	G	42	GENIC	homozygous	108638695
1	266854156	266854157	A	C	44	GENIC	homozygous	108638696
1	266855702	266855703	T	C	22	GENIC	homozygous	108638698
1	266855772	266855773	T	C	30	GENIC	homozygous	108638699
1	266856268	266856269	C	G	40	GENIC	homozygous	108638700
1	266858119	266858120	A	G	27	GENIC	homozygous	108638701
1	266858271	266858272	C	T	25	GENIC	homozygous	108638702
1	266858867	266858868	A	G	44	GENIC	homozygous	108638703
1	266858919	266858920	T	C	41	GENIC	homozygous	108638704
1	266859629	266859630	C	T	51	GENIC	homozygous	108638705
1	266859655	266859656	T	C	42	GENIC	homozygous	108638706