chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	95224911	95224912	T	C	21	GENIC	homozygous	50140854
13	95225003	95225004	A	G	24	GENIC	homozygous	50367106
13	95225629	95225630	C	A	25	GENIC	homozygous	50367108
13	95226733	95226734	C	T	18	GENIC	homozygous	50367110
13	95227115	95227116	G	A	29	GENIC	homozygous	50367112
13	95227539	95227540	A	C	39	GENIC	homozygous	50367115
13	95228064	95228065	C	T	32	GENIC	homozygous	50367117
13	95228736	95228737	G	A	32	GENIC	homozygous	50367119
13	95229737	95229738	C	G	43	GENIC	possibly homozygous	50367121
13	95229743	95229744	T	TC	29	GENIC	possibly homozygous	50140869
13	95229948	95229949	T	C	30	GENIC	possibly homozygous	50140871
13	95230120	95230121	C	T	18	GENIC	homozygous	50367123
13	95230205	95230206	C	T	24	GENIC	homozygous	50367125