chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	16392598	16392599	T	C	57	GENIC	homozygous	115270187
12	16393718	16393719	A	G	55	GENIC	homozygous	115270189
12	16393875	16393876	T	C	49	GENIC	homozygous	115270191
12	16394495	16394496	T	C	62	GENIC	homozygous	115270197
12	16394090	16394091	C	T	52	GENIC	homozygous	115270193
12	16394351	16394352	T	C	73	GENIC	homozygous	115270195
12	16394523	16394524	A	G	57	GENIC	homozygous	115270199
12	16396163	16396164	A	T	49	GENIC	homozygous	115364521
12	16396342	16396343	A	G	67	GENIC	homozygous	115270201
12	16396414	16396415	T	C	67	GENIC	homozygous	115270203
12	16397285	16397286	T	C	32	GENIC	possibly homozygous	131121128
12	16397553	16397554	T	G	29	GENIC	homozygous	115270207
12	16397623	16397624	T	C	25	GENIC	homozygous	115364522
12	16398119	16398120	A	G	38	GENIC	homozygous	115270209
12	16398266	16398267	G	A	56	GENIC	homozygous	115270211
12	16398299	16398300	A	G	59	GENIC	homozygous	115270213
12	16398414	16398415	C		58	GENIC	homozygous	128965950
12	16395875	16395876	C	T	30	GENIC	possibly homozygous	115421172
12	16395877	16395878	C	T	30	GENIC	possibly homozygous	115421174
12	16395889	16395889		T	32	GENIC	possibly homozygous	128965949