chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	47512202	47512203	G	A	49	GENIC	homozygous	118117927
8	47513649	47513650	C	A	40	GENIC	possibly homozygous	118117930
8	47514763	47514764	T	G	25	GENIC	homozygous	118117932
8	47516335	47516336	T	C	44	GENIC	homozygous	116953581
8	47518554	47518555	G	A	39	GENIC	homozygous	116953587
8	47518771	47518772	G	T	44	GENIC	homozygous	116953589
8	47518830	47518831	T	C	44	GENIC	homozygous	116953591
8	47520693	47520694	G	A	49	GENIC	homozygous	118117934
8	47522759	47522759		TGCCTA	42	GENIC	homozygous	131693219
8	47526990	47526991	T		49	GENIC	homozygous	131693225
8	47527718	47527719	T	G	47	GENIC	homozygous	116953621
8	47524356	47524357	C	T	51	GENIC	homozygous	118117936
8	47524551	47524552	G	A	37	GENIC	homozygous	116953611
8	47527492	47527493	C	A	52	GENIC	homozygous	116953615
8	47527496	47527497	T	A	51	GENIC	homozygous	116953617
8	47523638	47523639	A	C	19	GENIC	homozygous	118175245
8	47526003	47526004	T	C	48	GENIC	homozygous	118143301
8	47527759	47527760	T	C	53	GENIC	homozygous	118117938