chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	267608381	267608382	T	C	36	GENIC	homozygous	61200961
1	267608865	267608866	G	A	36	GENIC	homozygous	61200963
1	267609078	267609083	AGTGG	-----	26	GENIC	homozygous	61200965
1	267609122	267609123	T	-	28	GENIC	homozygous	61200969
1	267609168	267609169	G	A	33	GENIC	homozygous	61200971
1	267609295	267609296	G	GC	37	GENIC	homozygous	61200973
1	267609303	267609304	T	A	41	GENIC	homozygous	61200975
1	267609886	267609887	G	A	30	GENIC	homozygous	61200977
1	267610104	267610105	G	A	35	GENIC	homozygous	61200979
1	267610445	267610446	A	G	25	GENIC	homozygous	61200981
1	267610465	267610466	T	A	32	GENIC	homozygous	61200983
1	267611177	267611179	TT	--	17	GENIC	possibly homozygous	61200985
1	267612402	267612403	C	T	24	GENIC	homozygous	61200987
1	267612680	267612681	A	G	31	GENIC	homozygous	61200989
1	267613195	267613196	T	TTTC	28	GENIC	homozygous	61200991
1	267613531	267613532	A	T	30	GENIC	homozygous	61200993
1	267613647	267613648	G	C	35	GENIC	homozygous	61200995
1	267613824	267613825	T	-	35	GENIC	homozygous	61200997
1	267613849	267613850	G	GA	32	GENIC	homozygous	61200999
1	267614275	267614276	A	T	29	GENIC	homozygous	61201001
1	267614355	267614356	C	T	34	GENIC	homozygous	61201003
1	267614367	267614368	C	G	31	GENIC	homozygous	61201005
1	267615009	267615010	G	C	41	GENIC	homozygous	61201007
1	267615227	267615228	T	-	21	GENIC	possibly homozygous	61201009
1	267616354	267616355	G	A	34	GENIC	homozygous	61201011
1	267616383	267616384	C	T	31	GENIC	homozygous	61201013
1	267616569	267616570	C	T	32	GENIC	homozygous	61201015