chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	35090453	35090453		C	37	GENIC	homozygous	144431595
12	35090935	35090936	T	C	34	GENIC	homozygous	139135391
12	35090964	35090965	C	T	36	GENIC	homozygous	144435668
12	35091618	35091628	TTTTTTTTAA		43	GENIC	heterozygous	144431596
12	35091813	35091814	C	T	49	GENIC	possibly homozygous	144435669
12	35092116	35092117	A	T	48	GENIC	homozygous	144435670
12	35092243	35092244	C	T	54	GENIC	homozygous	144435671
12	35093121	35093122	C	T	45	GENIC	homozygous	144435672
12	35093554	35093555	T	A	45	GENIC	homozygous	139135394
12	35093745	35093746	A	G	31	GENIC	homozygous	139135395
12	35093785	35093785		GC	18	GENIC	homozygous	144431597
12	35093792	35093795	CGC		19	GENIC	homozygous	144431598
12	35093864	35093865	C	T	30	GENIC	homozygous	139135396
12	35093922	35093923	C	T	41	GENIC	homozygous	144435673
12	35094083	35094084	A	C	59	GENIC	homozygous	144435674
12	35094600	35094601	C	T	53	GENIC	homozygous	139135397
12	35095355	35095356	G	A	51	GENIC	homozygous	144435675
12	35093808	35093809	G		17	GENIC	heterozygous	403325748
12	35093808	35093809	G	A	17	GENIC	homozygous	403325747