chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	32456370	32456371	A	G	39	GENIC	homozygous	50443638
12	32456383	32456384	T	TGTGTGTG	28	GENIC	possibly homozygous	50933161
12	32456384	32456385	A	T	28	GENIC	possibly homozygous	50933164
12	32456442	32456443	G	C	49	GENIC	homozygous	50443640
12	32456560	32456561	A	AGT	20	GENIC	heterozygous	50541081
12	32456561	32456563	GT	--	20	GENIC	heterozygous	50541082
12	32456754	32456755	G	A	48	GENIC	homozygous	50933167
12	32459677	32459678	C	-	6	GENIC	homozygous	50175739
12	32460344	32460345	C	T	25	GENIC	homozygous	50933170
12	32460491	32460492	T	-	13	GENIC	homozygous	50933173
12	32460645	32460646	G	A	40	GENIC	homozygous	50933176
12	32460673	32460674	G	A	40	GENIC	homozygous	50933179
12	32461148	32461149	T	C	41	GENIC	homozygous	50443644
12	32461491	32461495	CTTC	----	10	GENIC	homozygous	50541083
12	32461749	32461763	CTCTCTCTCTCTCT	--------------	14	GENIC	heterozygous	50968036
12	32461751	32461763	CTCTCTCTCTCT	------------	14	GENIC	heterozygous	50933182
12	32462837	32462838	T	C	57	GENIC	homozygous	50443656
12	32462867	32462868	C	T	61	GENIC	homozygous	50443658
12	32463779	32463780	T	TACAC	63	GENIC	heterozygous	50443660
12	32463779	32463780	T	TAC	63	GENIC	possibly homozygous	50933185
12	32467820	32467822	AC	--	26	GENIC	heterozygous	50541084