chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	14782880	14782881	G	A	45	GENIC	homozygous	50069353
12	14783133	14783134	T	A	37	GENIC	homozygous	50069355
12	14783220	14783221	T	C	37	GENIC	homozygous	50069357
12	14783276	14783277	C	T	46	GENIC	homozygous	50069359
12	14783719	14783720	C	-	15	GENIC	possibly homozygous	50069361
12	14784151	14784152	G	GT	37	GENIC	possibly homozygous	50069363
12	14785166	14785167	T	C	39	GENIC	homozygous	50069365
12	14785176	14785177	T	C	50	GENIC	homozygous	50069367
12	14785400	14785401	A	G	38	GENIC	homozygous	50069369
12	14786221	14786222	G	T	20	GENIC	homozygous	50069371
12	14786222	14786223	G	T	19	GENIC	homozygous	50069373
12	14786582	14786583	T	C	40	GENIC	homozygous	50069375
12	14786617	14786618	A	G	49	GENIC	homozygous	50069377
12	14786794	14786795	G	C	50	GENIC	homozygous	50069379
12	14787810	14787811	C	T	49	GENIC	homozygous	50069381
12	14787852	14787853	G	A	41	GENIC	homozygous	50069383
12	14788167	14788169	AG	--	7	GENIC	homozygous	50069385
12	14788218	14788219	C	A	19	GENIC	possibly homozygous	50069387
12	14789181	14789190	TTTTTTTTG	---------	16	GENIC	heterozygous	50069389
12	14789189	14789190	G	-	22	GENIC	homozygous	50069391
12	14789205	14789206	C	T	20	GENIC	heterozygous	50069393
12	14789898	14789899	G	A	37	GENIC	homozygous	50069395