chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	121725412	121725413	A	G	40	GENIC	homozygous	112145004
3	121728207	121728208	G	A	25	GENIC	homozygous	112145008
3	121728767	121728768	C	T	23	GENIC	homozygous	112145012
3	121729350	121729351	T	A	17	GENIC	homozygous	112145015
3	121729823	121729824	C	T	29	GENIC	homozygous	112145017
3	121730138	121730139	C	T	26	GENIC	homozygous	112145019
3	121730387	121730388	T	G	27	GENIC	homozygous	111690013
3	121730623	121730624	A	G	14	GENIC	homozygous	111690014
3	121730661	121730662	A	G	18	GENIC	homozygous	112356522
3	121729074	121729075	A	G	23	GENIC	homozygous	112356516
3	121731842	121731843	A	T	34	GENIC	homozygous	112145024
3	121731860	121731861	T	C	39	GENIC	homozygous	112145026
3	121731874	121731875	A	G	39	GENIC	homozygous	112145028
3	121731936	121731937	A	G	25	GENIC	homozygous	112145030
3	121732326	121732327	T	C	24	GENIC	homozygous	112145032
3	121732341	121732342	T	C	26	GENIC	homozygous	111690017
3	121733069	121733070	C	T	26	GENIC	homozygous	112356528
3	121733526	121733527	T	C	29	GENIC	homozygous	112145034
3	121734372	121734373	G	A	21	GENIC	homozygous	112145036
3	121734729	121734730	C	G	33	GENIC	homozygous	112145038
3	121735684	121735685	G	A	25	GENIC	homozygous	112145040
3	121736254	121736255	C	T	24	GENIC	homozygous	112356530
3	121736369	121736370	G	A	22	GENIC	homozygous	112145042
3	121736710	121736711	C	T	29	GENIC	homozygous	112356532
3	121737236	121737237	C	T	19	GENIC	homozygous	112145046
3	121737283	121737284	G	A	16	GENIC	homozygous	112145048
3	121738503	121738504	T	C	25	GENIC	homozygous	112145052