chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	19330513	19330514	A	-	19	GENIC	homozygous	50368645
12	19330895	19330929	CGCACGCACGCACGCACGCACGCACGCACGCACG	----------------------------------	9	GENIC	heterozygous	50536689
12	19331155	19331156	G	T	20	GENIC	homozygous	50368651
12	19331356	19331357	A	G	25	GENIC	homozygous	50368653
12	19331634	19331635	T	C	23	GENIC	homozygous	50368655
12	19331771	19331772	T	C	24	GENIC	homozygous	50368657
12	19332106	19332107	T	C	28	GENIC	homozygous	50368659
12	19332949	19332950	C	T	25	GENIC	homozygous	50368661
12	19333153	19333154	A	G	33	GENIC	possibly homozygous	50368663
12	19333235	19333236	T	C	33	GENIC	homozygous	50368665
12	19333328	19333329	T	C	43	GENIC	homozygous	50098673
12	19334026	19334027	A	G	33	GENIC	homozygous	50098675
12	19334642	19334643	G	GGGGTGT	6	GENIC	heterozygous	50098681
12	19334642	19334643	G	GGGGT	6	GENIC	heterozygous	50607196
12	19335795	19335796	A	G	28	GENIC	homozygous	50368670
12	19336271	19336272	T	C	22	GENIC	homozygous	50098683
12	19336565	19336566	T	TGCA	9	GENIC	homozygous	50368672
12	19337560	19337564	GCCT	----	28	GENIC	homozygous	50098685
12	19337917	19337918	G	A	40	GENIC	homozygous	50368674
12	19338930	19338931	T	C	21	GENIC	homozygous	50098689
12	19340291	19340292	A	G	30	GENIC	homozygous	50098699
12	19341298	19341299	A	T	36	GENIC	homozygous	50098701
12	19341300	19341301	T	G	36	GENIC	homozygous	50098703
12	19341477	19341478	A	G	24	GENIC	homozygous	50098707
12	19342154	19342159	GTGGG	-----	22	GENIC	homozygous	50098713
12	19343288	19343289	C	T	44	GENIC	homozygous	50098719
12	19344133	19344134	G	A	21	GENIC	homozygous	50368686
12	19344414	19344415	G	C	27	GENIC	homozygous	50098721
12	19344497	19344498	T	C	30	GENIC	homozygous	50098723
12	19344944	19344946	AC	--	35	GENIC	homozygous	50098727