chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	46798522	46798526	AACA		53	GENIC	homozygous	128996730
12	46799526	46799527	T	C	41	GENIC	homozygous	115342551
12	46801416	46801417	G	C	40	GENIC	homozygous	115396992
12	46802661	46802662	A	G	46	GENIC	homozygous	115342553
12	46807417	46807418	C	T	40	GENIC	homozygous	115342557
12	46821658	46821672	CCACCCCACCCCAC		28	GENIC	homozygous	128996731
12	46827878	46827879	T	G	46	GENIC	homozygous	115342559
12	46825078	46825079	A		27	GENIC	heterozygous	131915274
12	46811877	46811878	T	C	43	GENIC	possibly homozygous	115444205
12	46825042	46825043	C	T	35	GENIC	homozygous	118272499
12	46828324	46828350	TGCATGTGTGCGTGTGTGTGCATGCA		38	GENIC	homozygous	128996732
12	46828624	46828625	T	C	21	GENIC	possibly homozygous	115567677
12	46829121	46829121		TGGA	34	GENIC	homozygous	128996733
12	46831119	46831120	A	G	5	GENIC	homozygous	118272502
12	46831250	46831251	T	C	35	GENIC	homozygous	115397078
12	46831387	46831388	C	T	26	GENIC	homozygous	115342561
12	46831390	46831391	C	G	26	GENIC	homozygous	115342563
12	46832755	46832756	A		33	GENIC	possibly homozygous	128996734
12	46832972	46832973	T	G	36	GENIC	homozygous	115444206
12	46834144	46834145	T	C	17	GENIC	homozygous	115452031
12	46842884	46842885	A	G	28	GENIC	homozygous	115342565
12	46843428	46843429	C		41	GENIC	homozygous	128996735
12	46844860	46844861	G	T	39	GENIC	homozygous	115342567