chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	71503022	71503023	G	T	21	GENIC	homozygous	52673646
8	71503024	71503025	G	T	21	GENIC	homozygous	52673647
8	71503090	71503091	G	-	22	GENIC	homozygous	52673648
8	71504165	71504166	G	GT	12	GENIC	homozygous	52673649
8	71509641	71509642	G	A	54	GENIC	heterozygous	53212462
8	71509685	71509686	T	C	68	GENIC	heterozygous	53212463
8	71509700	71509701	T	G	64	GENIC	heterozygous	53212464
8	71524489	71524491	GT	--	11	GENIC	heterozygous	52673655
8	71525422	71525423	G	T	23	GENIC	possibly homozygous	52673656
8	71528664	71528667	CCC	---	14	GENIC	heterozygous	52673657
8	71528666	71528667	C	-	14	GENIC	possibly homozygous	52673658
8	71528695	71528696	G	A	16	GENIC	heterozygous	52673659
8	71545193	71545194	C	A	17	GENIC	homozygous	52673660
8	71546665	71546666	A	G	16	GENIC	heterozygous	52673661
8	71546770	71546771	A	AGC	21	GENIC	homozygous	52673662
8	71585279	71585280	G	C	26	GENIC	possibly homozygous	52673664
8	71590498	71590499	T	-	19	GENIC	homozygous	52673665
8	71590501	71590502	G	GA	20	GENIC	homozygous	52673666
8	71590504	71590505	G	T	21	GENIC	homozygous	52673667
8	71603455	71603457	AC	--	7	GENIC	heterozygous	52673668