chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	16392598	16392599	T	C	69	GENIC	possibly homozygous	115270187
12	16393562	16393563	T	C	42	GENIC	heterozygous	118246354
12	16393571	16393572	T	C	39	GENIC	heterozygous	118246355
12	16393718	16393719	A	G	44	GENIC	homozygous	115270189
12	16393875	16393876	T	C	51	GENIC	homozygous	115270191
12	16394090	16394091	C	T	38	GENIC	homozygous	115270193
12	16394351	16394352	T	C	78	GENIC	homozygous	115270195
12	16394495	16394496	T	C	52	GENIC	homozygous	115270197
12	16394523	16394524	A	G	58	GENIC	homozygous	115270199
12	16395875	16395876	C	T	36	GENIC	heterozygous	115421172
12	16395877	16395878	C	T	38	GENIC	possibly homozygous	115421174
12	16395889	16395890	A	T	45	GENIC	homozygous	118246356
12	16396342	16396343	A	G	63	GENIC	homozygous	115270201
12	16396414	16396415	T	C	64	GENIC	homozygous	115270203
12	16396744	16396745	T	G	56	GENIC	heterozygous	118246357
12	16396764	16396765	G	A	57	GENIC	heterozygous	118292833
12	16393545	16393546	C	T	49	GENIC	heterozygous	118292829
12	16393554	16393555	T	C	46	GENIC	heterozygous	118292830
12	16396688	16396689	C	T	72	GENIC	heterozygous	118292832
12	16396163	16396164	A	T	42	GENIC	homozygous	115364521
12	16397277	16397278	T	C	56	GENIC	heterozygous	115421176
12	16397287	16397288	T	C	53	GENIC	heterozygous	115270205
12	16397553	16397554	T	G	37	GENIC	homozygous	115270207
12	16397579	16397580	A	G	32	GENIC	possibly homozygous	115505258
12	16397623	16397624	T	C	27	GENIC	homozygous	115364522
12	16398119	16398120	A	G	58	GENIC	homozygous	115270209
12	16398266	16398267	G	A	45	GENIC	homozygous	115270211
12	16398299	16398300	A	G	45	GENIC	homozygous	115270213
12	16393560	16393561	T	C	44	GENIC	heterozygous	118292831