chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	86344799	86344799		CGAGCTGCC	10	GENIC	homozygous	128841950
10	86344807	86344807		GACTCT	12	GENIC	homozygous	128841951
10	86344811	86344811		A	10	GENIC	homozygous	128841952
10	86344813	86344813		CCCAG	9	GENIC	homozygous	128841953
10	86344816	86344817	T	C	11	GENIC	homozygous	128872805
10	86344829	86344830	C		14	GENIC	homozygous	128841954
10	86344838	86344839	C	A	15	GENIC	homozygous	128872806
10	86344847	86344848	C		16	GENIC	heterozygous	128841955
10	86353156	86353158	TT		23	GENIC	homozygous	128841956
10	86353168	86353168		AGATC	19	GENIC	homozygous	128841957
10	86353174	86353174		CCCAGCTG	17	GENIC	homozygous	128841958
10	86353175	86353180	TTTAT		13	GENIC	homozygous	128841959
10	86353182	86353182		AGAG	13	GENIC	homozygous	128841960
10	86353186	86353190	TTTT		11	GENIC	homozygous	128841961
10	86353158	86353159	T	G	23	GENIC	homozygous	116898667
10	86353160	86353161	T	G	23	GENIC	homozygous	116898669
10	86353162	86353163	C	A	21	GENIC	homozygous	116898671
10	86353171	86353172	T	C	17	GENIC	homozygous	116898673
10	86353184	86353185	T	G	11	GENIC	homozygous	116898675
10	86353192	86353192		GGG	11	GENIC	homozygous	128841962
10	86353196	86353200	TTTT		9	GENIC	homozygous	128841963
10	86353686	86353687	A	G	2	GENIC	homozygous	134143059