chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	135555735	135555736	T	C	79	GENIC	homozygous	114018179
5	135555971	135555972	A	G	68	GENIC	possibly homozygous	114018180
5	135555981	135555982	A	T	71	GENIC	homozygous	114018181
5	135556391	135556392	G	C	52	GENIC	homozygous	114018182
5	135557381	135557382	T	C	42	GENIC	homozygous	114018183
5	135557595	135557596	T	A	41	GENIC	homozygous	114018184
5	135558239	135558240	A	C	60	GENIC	homozygous	114018187
5	135558241	135558242	G	C	58	GENIC	homozygous	114018188
5	135558617	135558618	C	T	56	GENIC	homozygous	114018190
5	135558957	135558958	G	T	85	GENIC	homozygous	114018191
5	135559336	135559337	C	T	64	GENIC	homozygous	114018192
5	135559561	135559562	G	A	52	GENIC	homozygous	114144586
5	135559563	135559564	G	A	53	GENIC	homozygous	114144587
5	135559641	135559642	C	T	40	GENIC	homozygous	114018193
5	135559766	135559767	G	A	28	GENIC	heterozygous	114018194
5	135559814	135559815	A	G	19	GENIC	possibly homozygous	114018195
5	135560377	135560378	T	C	47	GENIC	homozygous	114018199
5	135560698	135560699	T	A	67	GENIC	homozygous	114018200
5	135560701	135560702	C	T	70	GENIC	homozygous	114018201