chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	101476216	101476217	C	A	10	GENIC	homozygous	66168221
13	101476217	101476218	C	G	10	GENIC	homozygous	66168224
13	101476218	101476219	C	G	10	GENIC	homozygous	66168227
13	101476219	101476220	C	G	9	GENIC	homozygous	66168230
13	101476220	101476221	C	T	8	GENIC	homozygous	66168233
13	101488049	101488050	C	T	93	GENIC	heterozygous	66168245
13	101488088	101488089	C	T	43	GENIC	possibly homozygous	66168248
13	101488097	101488098	C	T	37	GENIC	possibly homozygous	66168251
13	101488151	101488152	C	T	20	GENIC	homozygous	66168253
13	101488172	101488173	A	T	28	GENIC	homozygous	66168256
13	101488184	101488185	C	T	33	GENIC	possibly homozygous	66168259