chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	1460958	1460959	A	G	39	GENIC	homozygous	115232254
12	1462370	1462371	C	T	44	GENIC	homozygous	115357073
12	1466134	1466135	A	C	42	GENIC	possibly homozygous	115232262
12	1466254	1466255	A	T	37	GENIC	homozygous	115232264
12	1466606	1466607	A	G	46	GENIC	homozygous	115232266
12	1468081	1468082	C	T	39	GENIC	homozygous	115232268
12	1468907	1468908	C	T	43	GENIC	homozygous	115357074
12	1470541	1470542	T	A	43	GENIC	possibly homozygous	115357075
12	1469750	1469750		GTGTCTGT	41	GENIC	homozygous	132164426
12	1468402	1468406	GTGT		36	GENIC	homozygous	128948593