chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	282142514	282142515	A	T	33	GENIC	homozygous	108670827
1	282144368	282144369	G	A	31	GENIC	homozygous	108670828
1	282144486	282144487	A	C	32	GENIC	homozygous	108670829
1	282144863	282144864	A	G	32	GENIC	homozygous	108670830
1	282145471	282145472	A	T	33	GENIC	homozygous	108670831
1	282148607	282148608	G	A	31	GENIC	homozygous	108670832
1	282150641	282150642	C	T	19	GENIC	homozygous	108670833
1	282151239	282151240	T	C	43	GENIC	homozygous	108670834
1	282152445	282152446	A	G	38	GENIC	possibly homozygous	108670835
1	282152616	282152617	T	A	26	GENIC	homozygous	108670836
1	282152971	282152972	T	C	29	GENIC	homozygous	108670837
1	282153710	282153711	T	C	28	GENIC	homozygous	108670838
1	282156377	282156378	A	T	21	GENIC	homozygous	108670839
1	282156443	282156444	T	C	24	GENIC	homozygous	108670840
1	282157370	282157371	A	G	22	GENIC	homozygous	108670841
1	282162332	282162333	C	T	26	GENIC	homozygous	108670842
1	282162800	282162801	G	A	28	GENIC	homozygous	108670843
1	282165523	282165524	C	G	41	GENIC	homozygous	108670844
1	282166029	282166030	C	G	28	GENIC	homozygous	108670845
1	282169541	282169542	C	G	35	GENIC	possibly homozygous	108670846