chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	200091092	200091093	C	T	12	GENIC	homozygous	108502954
1	200092336	200092337	T	C	22	GENIC	homozygous	108502958
1	200098783	200098784	C	A	11	GENIC	homozygous	108502962
1	200101883	200101884	T	A	16	GENIC	homozygous	108502964
1	200102768	200102769	A	G	7	GENIC	homozygous	108502968
1	200103259	200103260	A	G	32	GENIC	homozygous	108502970
1	200103287	200103288	A	G	36	GENIC	homozygous	108502972
1	200103734	200103735	C	A	16	GENIC	homozygous	108502974
1	200105292	200105293	G	A	17	GENIC	homozygous	108502976
1	200107695	200107696	T	C	15	GENIC	homozygous	108502980
1	200108550	200108551	G	A	7	GENIC	homozygous	108502982
1	200111121	200111122	C	T	23	GENIC	homozygous	108502984
1	200111280	200111281	G	A	20	GENIC	homozygous	108502986
1	200111928	200111929	T	C	21	GENIC	homozygous	108502988
1	200112449	200112450	A	G	23	GENIC	homozygous	108502990
1	200112829	200112830	A	G	6	GENIC	homozygous	108502992
1	200114822	200114823	G	A	20	GENIC	homozygous	108502994
1	200115095	200115096	G	C	21	GENIC	homozygous	108502996
1	200115478	200115479	T	C	22	GENIC	homozygous	108502998
1	200116078	200116079	G	A	27	GENIC	homozygous	108503000
1	200116373	200116374	G	A	32	GENIC	homozygous	108503002