chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	124123461	124123462	G	A	17	GENIC	homozygous	114976907
6	124123683	124123684	G	A	23	GENIC	homozygous	114976908
6	124123942	124123943	C	A	25	GENIC	homozygous	114976909
6	124124267	124124268	T	G	25	GENIC	homozygous	114976910
6	124124369	124124370	G	C	17	GENIC	possibly homozygous	114976911
6	124124837	124124838	C	G	16	GENIC	homozygous	114976912
6	124124864	124124865	T	G	24	GENIC	homozygous	114976913
6	124124919	124124920	C	T	24	GENIC	homozygous	114976914
6	124126653	124126654	G	A	16	GENIC	homozygous	114976915
6	124127089	124127090	T	A	12	GENIC	homozygous	114976916
6	124130974	124130975	C	T	30	GENIC	homozygous	114976917
6	124133945	124133946	T	C	29	GENIC	homozygous	114976918
6	124135563	124135564	C	T	22	GENIC	homozygous	114976919
6	124125047	124125047		TATATG	18	GENIC	homozygous	128391814
6	124130118	124130129	CTTTGCTTCCC		37	GENIC	homozygous	128391815
6	124133055	124133059	GACT		20	GENIC	homozygous	128391816
6	124133979	124133980	T		31	GENIC	homozygous	128391817