chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	93197958	93197959	G	T	15	GENIC	homozygous	117388682
9	93205563	93205564	A	C	46	GENIC	possibly homozygous	117600472
9	93241084	93241085	G	T	19	GENIC	possibly homozygous	117388712
9	93265704	93265705	C	T	31	GENIC	homozygous	117388732
9	93270172	93270173	C	T	34	GENIC	heterozygous	117828922
9	93271520	93271521	T	G	21	GENIC	homozygous	117388744
9	93271589	93271590	C	G	26	GENIC	homozygous	117388745
9	93271646	93271647	T	G	30	GENIC	homozygous	117388747
9	93281996	93281997	A	C	30	GENIC	heterozygous	117600474
9	93286293	93286294	C	A	32	GENIC	heterozygous	117388767
9	93286299	93286300	T	C	37	GENIC	heterozygous	117388768
9	93287680	93287681	G	T	24	GENIC	heterozygous	117388769
9	93287683	93287684	G	T	26	GENIC	heterozygous	117388770
9	93292574	93292575	T	C	15	GENIC	heterozygous	117801029
9	93295595	93295596	T	G	40	GENIC	homozygous	117388784
9	93298495	93298496	A	G	29	GENIC	homozygous	117388790
9	93299025	93299026	G	A	29	GENIC	homozygous	117600476