chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	35090935	35090936	T	C	34	GENIC	homozygous	139135391
12	35091463	35091464	A	G	40	GENIC	homozygous	147004040
12	35091813	35091814	C	T	32	GENIC	possibly homozygous	144435669
12	35092116	35092117	A	T	43	GENIC	homozygous	144435670
12	35092243	35092244	C	T	55	GENIC	homozygous	144435671
12	35093121	35093122	C	T	63	GENIC	homozygous	144435672
12	35093745	35093746	A	G	40	GENIC	homozygous	139135395
12	35093864	35093865	C	T	35	GENIC	homozygous	139135396
12	35094083	35094084	A	C	51	GENIC	homozygous	144435674
12	35094600	35094601	C	T	38	GENIC	homozygous	139135397
12	35093459	35093460	G		46	GENIC	homozygous	147000114
12	35093808	35093809	G		27	GENIC	possibly homozygous	403325748
12	35093808	35093809	G	A	27	GENIC	heterozygous	403325747