chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	20690603	20690604	A	T	41	GENIC	homozygous	139107830
12	20690956	20690957	A		21	GENIC	heterozygous	403643994
12	20691033	20691034	T	C	47	GENIC	possibly homozygous	142322677
12	20691126	20691127	T	C	60	GENIC	homozygous	139107832
12	20691358	20691359	C	T	50	GENIC	homozygous	139107833
12	20691601	20691602	T	C	51	GENIC	homozygous	139107834
12	20695196	20695197	C	T	60	GENIC	homozygous	142322678
12	20695823	20695824	A	C	43	GENIC	possibly homozygous	142322679
12	20695863	20695864	C	T	43	GENIC	possibly homozygous	142322680
12	20696998	20696999	T	C	64	GENIC	homozygous	139107842
12	20697009	20697010	T	C	61	GENIC	homozygous	139107843
12	20697245	20697246	G	C	61	GENIC	homozygous	142322681
12	20696015	20696016	C		20	GENIC	heterozygous	403320317
12	20690956	20690957	A	G	21	GENIC	heterozygous	403643995
12	20690969	20690970	T		22	GENIC	heterozygous	403940700
12	20690969	20690970	T	G	22	GENIC	heterozygous	403940701
12	20692761	20692762	C		34	GENIC	homozygous	139046285
12	20693840	20693843	GAA		38	GENIC	homozygous	139046286
12	20695995	20695995		AAAAAA	16	GENIC	homozygous	139046288
12	20692777	20692777		G	35	GENIC	possibly homozygous	142310099
12	20696015	20696016	C	A	20	GENIC	homozygous	403320316