chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	84389088	84389089	T	C	26	GENIC	homozygous	142170026
9	84389097	84389098	C	A	25	GENIC	homozygous	142170027
9	84389138	84389139	G	A	25	GENIC	homozygous	142170028
9	84389154	84389155	T	C	23	GENIC	homozygous	142170029
9	84389348	84389349	G	C	20	GENIC	homozygous	142170030
9	84389503	84389504	T		24	GENIC	possibly homozygous	142117831
9	84389729	84389730	G	A	13	GENIC	homozygous	146927853
9	84389742	84389743	G	A	15	GENIC	homozygous	142170031
9	84389753	84389754	C	T	14	GENIC	homozygous	142170032
9	84389774	84389775	T	A	18	GENIC	homozygous	142170033
9	84389776	84389777	G	A	18	GENIC	homozygous	142170034
9	84389791	84389792	A	T	18	GENIC	homozygous	142170035
9	84389810	84389811	C	A	21	GENIC	possibly homozygous	142170036
9	84389925	84389926	C	T	22	GENIC	possibly homozygous	142170037
9	84390073	84390074	G	T	16	GENIC	homozygous	142170038
9	84390204	84390205	C	A	17	GENIC	homozygous	142170039
9	84390306	84390307	C	T	18	GENIC	homozygous	142170040
9	84390398	84390399	A	G	21	GENIC	homozygous	142170041
9	84390415	84390416	C	T	22	GENIC	homozygous	142170042
9	84390529	84390530	T	A	20	GENIC	homozygous	142170043
9	84390578	84390579	T	C	25	GENIC	homozygous	142170044
9	84390600	84390601	C	T	21	GENIC	homozygous	142170045
9	84390613	84390614	G		23	GENIC	homozygous	142117832
9	84390634	84390635	T	C	23	GENIC	homozygous	142170046
9	84390866	84390867	T	G	18	GENIC	homozygous	142170047
9	84391011	84391012	G	C	16	GENIC	homozygous	142170048
9	84391143	84391144	C	T	12	GENIC	homozygous	142170049
9	84391337	84391338	A	G	19	GENIC	homozygous	142170050