chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	57060128	57060129	T	C	42	GENIC	homozygous	116784909
10	57060416	57060417	G	A	62	GENIC	homozygous	117060089
10	57060655	57060656	A	G	38	GENIC	homozygous	116603123
10	57060852	57060853	C	T	42	GENIC	homozygous	117060091
10	57061025	57061026	T	C	39	GENIC	homozygous	116784911
10	57061122	57061123	A	T	52	GENIC	homozygous	116784913
10	57061404	57061405	A	G	54	GENIC	homozygous	116784915
10	57061500	57061501	A	G	49	GENIC	homozygous	116784917
10	57062986	57062987	T	A	34	GENIC	homozygous	117060093
10	57063315	57063316	T	C	49	GENIC	homozygous	116784919
10	57063534	57063535	T	C	56	GENIC	homozygous	116784921
10	57064163	57064164	A	T	48	GENIC	homozygous	116784923
10	57062736	57062736		G	13	GENIC	homozygous	128819428
10	57063853	57063853		CGACTTGGA	56	GENIC	homozygous	131094701
10	57064230	57064230		C	49	GENIC	homozygous	131094702