chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42766200	42766201	T	C	18	GENIC	homozygous	67255056
12	42766204	42766205	A	C	19	GENIC	possibly homozygous	67657592
12	42766208	42766209	A	C	19	GENIC	possibly homozygous	66755324
12	42766212	42766213	A	C	17	GENIC	possibly homozygous	66755326
12	42766216	42766217	A	C	18	GENIC	homozygous	66755328
12	42766220	42766221	A	C	18	GENIC	homozygous	66755330
12	42766224	42766225	A	C	17	GENIC	homozygous	66755332
12	42766228	42766229	A	C	17	GENIC	possibly homozygous	66755334
12	42766232	42766233	A	C	17	GENIC	heterozygous	66755336
12	42767079	42767080	C	A	33	GENIC	homozygous	66755338
12	42768049	42768050	A	T	30	GENIC	possibly homozygous	66755340
12	42768453	42768454	T	C	39	GENIC	homozygous	66755342
12	42770760	42770761	A	C	30	GENIC	homozygous	66755344
12	42771511	42771512	C	A	15	GENIC	homozygous	66755346
12	42766236	42766237	A	C	17	GENIC	heterozygous	66881057