chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	9422272	9422273	A	G	65	GENIC	homozygous	143527375
12	9422820	9422821	C	G	45	GENIC	homozygous	145773099
12	9422959	9422960	G	C	46	GENIC	homozygous	143527376
12	9423433	9423434	T	C	40	GENIC	homozygous	139079866
12	9424330	9424331	C	T	59	GENIC	homozygous	145773100
12	9424370	9424371	C	T	61	GENIC	homozygous	145773101
12	9424434	9424435	A	G	46	GENIC	homozygous	143527378
12	9424462	9424463	G		35	GENIC	possibly homozygous	403315494
12	9423322	9423323	G		36	GENIC	homozygous	403315493
12	9424462	9424463	G	T	35	GENIC	heterozygous	154752474
12	9424750	9424751	T	C	34	GENIC	homozygous	139079870
12	9425535	9425536	T	C	67	GENIC	homozygous	139079871
12	9425665	9425666	C	T	64	GENIC	homozygous	145773102
12	9425677	9425678	A	G	61	GENIC	homozygous	139079872
12	9425692	9425693	A	G	66	GENIC	homozygous	139079873
12	9426665	9426666	G	A	55	GENIC	homozygous	139079875
12	9426885	9426886	G		12	GENIC	heterozygous	403315495
12	9426885	9426886	G	A	12	GENIC	homozygous	403315496
12	9426947	9426948	T	C	32	GENIC	homozygous	139079877
12	9427867	9427868	G	A	66	GENIC	homozygous	139079878
12	9428032	9428033	T	C	59	GENIC	homozygous	139079879
12	9428049	9428050	T	C	67	GENIC	homozygous	139079880
12	9423322	9423323	G	A	36	GENIC	heterozygous	403315492
12	9424446	9424446		GG	44	GENIC	homozygous	145770432
12	9424460	9424463	TTG		32	GENIC	heterozygous	145770433