chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	54073946	54073947	C	CAT	18	GENIC	homozygous	52636105
8	54074742	54074743	C	T	35	GENIC	homozygous	53698274
8	54074965	54074966	G	T	21	GENIC	homozygous	53698275
8	54075301	54075302	C	T	16	GENIC	homozygous	53698276
8	54075980	54075981	C	T	21	GENIC	homozygous	53698277
8	54077548	54077549	T	A	21	GENIC	homozygous	53698278
8	54077770	54077771	T	C	24	GENIC	homozygous	52636109
8	54078430	54078431	T	-	13	GENIC	homozygous	52976706
8	54078814	54078816	TG	--	1	GENIC	homozygous	53964046
8	54078829	54078830	G	GTC	1	GENIC	homozygous	53964048
8	54078838	54078840	TG	--	1	GENIC	homozygous	53964050
8	54078849	54078850	C	CTG	1	GENIC	homozygous	53964052
8	54078879	54078880	C	G	22	GENIC	homozygous	53698279
8	54080482	54080483	C	T	17	GENIC	homozygous	53698280
8	54080731	54080732	T	C	17	GENIC	homozygous	52636123
8	54080869	54080870	C	T	14	GENIC	homozygous	53698281
8	54080908	54080909	A	G	21	GENIC	homozygous	53698282
8	54083825	54083826	G	GA	9	GENIC	heterozygous	52976716
8	54084141	54084142	A	C	16	GENIC	homozygous	53698283
8	54084554	54084555	A	G	25	GENIC	homozygous	52636133