chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	56626243	56626244	A	G	17	GENIC	homozygous	116783730
10	56628059	56628060	A	G	9	GENIC	homozygous	116783732
10	56629118	56629119	C	T	4	GENIC	homozygous	116783734
10	56629388	56629389	T	C	10	GENIC	homozygous	116783736
10	56629784	56629785	C	T	9	GENIC	homozygous	116783738
10	56632300	56632301	C	T	6	GENIC	homozygous	116783740
10	56632480	56632481	C	A	3	GENIC	homozygous	116783742
10	56633748	56633749	C	T	9	GENIC	homozygous	116783744
10	56633802	56633803	C	T	13	GENIC	homozygous	116783746
10	56633957	56633958	A	G	6	GENIC	homozygous	116783748
10	56634368	56634369	A	T	17	GENIC	homozygous	116783750
10	56634675	56634676	G	A	8	GENIC	homozygous	116783752
10	56634682	56634683	T	G	9	GENIC	homozygous	116783754
10	56634944	56634945	G	T	6	GENIC	homozygous	116783756
10	56638861	56638862	C	T	11	GENIC	homozygous	116783758
10	56639293	56639294	A	G	10	GENIC	homozygous	116783760
10	56640228	56640229	A	G	12	GENIC	homozygous	116783762
10	56640386	56640387	T	C	8	GENIC	homozygous	116783764
10	56640741	56640742	T	C	11	GENIC	homozygous	116783766
10	56642841	56642842	A	G	13	GENIC	homozygous	116783768
10	56644495	56644496	C	T	14	GENIC	homozygous	116783770
10	56644510	56644511	T	G	15	GENIC	homozygous	116783772
10	56645715	56645716	T	A	9	GENIC	homozygous	116783774
10	56646258	56646259	C	T	13	GENIC	homozygous	116783776
10	56646594	56646595	T	C	12	GENIC	homozygous	116783778
10	56646981	56646982	A	T	8	GENIC	homozygous	116783780
10	56647519	56647520	T	C	6	GENIC	homozygous	116783782
10	56648921	56648922	G	A	13	GENIC	homozygous	116783784
10	56649815	56649816	T	C	11	GENIC	homozygous	116783786
10	56651383	56651384	T	C	3	GENIC	homozygous	116783788
10	56651883	56651884	G	A	9	GENIC	homozygous	116783791
10	56654085	56654086	A	T	12	GENIC	homozygous	116783793