chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	14782427	14782428	C	CGCCCT	5	GENIC	homozygous	50434583
12	14782588	14782589	A	AACACACACACACACACACACACACACACAC	3	GENIC	homozygous	50533266
12	14783696	14783697	T	TCTCTCTCACACACACA	16	GENIC	homozygous	50533270
12	14784148	14784149	G	GT	19	GENIC	homozygous	50434585
12	14784151	14784152	G	GT	21	GENIC	possibly homozygous	50069363
12	14785166	14785167	T	C	37	GENIC	homozygous	50069365
12	14785176	14785177	T	C	37	GENIC	homozygous	50069367
12	14785400	14785401	A	G	33	GENIC	homozygous	50069369
12	14786582	14786583	T	C	41	GENIC	homozygous	50069375
12	14786794	14786795	G	C	20	GENIC	homozygous	50069379
12	14787810	14787811	C	T	24	GENIC	homozygous	50069381
12	14788159	14788160	A	G	1	GENIC	homozygous	50533276
12	14788163	14788164	A	G	1	GENIC	homozygous	50533278
12	14788201	14788202	G	A	8	GENIC	heterozygous	50533280
12	14788277	14788278	C	A	17	GENIC	homozygous	50434587
12	14788746	14788747	G	T	30	GENIC	homozygous	50434589
12	14788891	14788892	C	T	35	GENIC	homozygous	50434591
12	14789181	14789190	TTTTTTTTG	---------	20	GENIC	possibly homozygous	50069389
12	14788215	14788219	GAGC	----	6	GENIC	homozygous	50503971
12	14789726	14789727	C	A	36	GENIC	homozygous	50434593
12	14790627	14790628	C	CA	36	GENIC	homozygous	50434595