chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	99372643	99372644	C	T	25	GENIC	homozygous	54491024
7	99372961	99372962	T	C	10	GENIC	homozygous	54491026
7	99373029	99373030	A	G	15	GENIC	homozygous	54491028
7	99373636	99373637	T	C	13	GENIC	homozygous	54491030
7	99373872	99373873	T	TTGTC	26	GENIC	homozygous	54491032
7	99374646	99374647	A	G	16	GENIC	homozygous	54491034
7	99375172	99375173	T	C	24	GENIC	homozygous	54491036
7	99375296	99375297	G	A	17	GENIC	homozygous	54491038
7	99375908	99375909	T	C	11	GENIC	homozygous	54491040
7	99376266	99376267	T	TA	8	GENIC	homozygous	54491042
7	99377623	99377624	G	GA	10	GENIC	possibly homozygous	54491044
7	99377663	99377664	A	AT	14	GENIC	homozygous	54491046
7	99378279	99378281	CT	--	16	GENIC	homozygous	54491048
7	99378532	99378533	T	G	10	GENIC	homozygous	54491050
7	99378585	99378589	TAGA	----	7	GENIC	homozygous	54491052
7	99380041	99380042	A	G	28	GENIC	homozygous	54491054
7	99381493	99381494	C	T	31	GENIC	homozygous	54491056