chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	101475918	101475919	G	C	12	GENIC	homozygous	66168197
13	101475923	101475924	C	A	4	GENIC	homozygous	66168200
13	101475964	101475965	G	T	6	GENIC	homozygous	66168206
13	101476035	101476036	C	G	20	GENIC	homozygous	66168209
13	101476038	101476039	C	A	23	GENIC	homozygous	66168212
13	101476095	101476096	C	A	20	GENIC	homozygous	66168215
13	101476101	101476102	C	A	20	GENIC	homozygous	66168218
13	101488049	101488050	C	T	41	GENIC	heterozygous	66168245
13	101488088	101488089	C	T	7	GENIC	heterozygous	66168248
13	101488097	101488098	C	T	7	GENIC	possibly homozygous	66168251
13	101488151	101488152	C	T	7	GENIC	homozygous	66168253
13	101488172	101488173	A	T	6	GENIC	homozygous	66168256
13	101488184	101488185	C	T	15	GENIC	possibly homozygous	66168259