chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	78640802	78640803	G	C	24	INTERGENIC	homozygous	48803830
14	78642565	78642566	A	G	11	INTERGENIC	homozygous	48803831
14	78642711	78642712	T	A	14	INTERGENIC	homozygous	48803832
14	78642975	78642976	T	C	29	INTERGENIC	homozygous	48803833
14	78643139	78643140	A	-	19	INTERGENIC	possibly homozygous	48803834
14	78643920	78643921	C	T	30	INTERGENIC	homozygous	48803835
14	78646144	78646150	TGTGTG	------	6	GENIC	heterozygous	49327230
14	78646146	78646150	TGTG	----	6	GENIC	heterozygous	49315603
14	78647727	78647728	T	C	33	GENIC	homozygous	48803837
14	78649698	78649699	G	A	34	GENIC	homozygous	48803838
14	78650159	78650160	A	G	27	GENIC	homozygous	48803839
14	78651400	78651401	A	G	18	GENIC	homozygous	48803840
14	78651807	78651808	G	A	28	GENIC	homozygous	48803841
14	78652817	78652818	A	G	31	GENIC	possibly homozygous	48803842
14	78655738	78655739	G	GA	2	GENIC	homozygous	49013488
14	78655933	78655935	GG	--	16	GENIC	homozygous	48803843
14	78656192	78656216	TCTCAATCTCTCTCTCTCTCTCTC	------------------------	15	GENIC	heterozygous	49315605
14	78656194	78656216	TCAATCTCTCTCTCTCTCTCTC	----------------------	15	GENIC	heterozygous	49315606
14	78657289	78657290	T	C	31	GENIC	homozygous	48803845
14	78658111	78658112	A	G	15	GENIC	homozygous	48803846
14	78660122	78660123	T	C	33	GENIC	homozygous	48803847
14	78660160	78660161	G	A	31	GENIC	possibly homozygous	48803848
14	78660704	78660705	A	ACAGGAGCCTGCTCTTCC	12	GENIC	homozygous	49292013
14	78661283	78661284	G	A	27	GENIC	homozygous	48803851
14	78661484	78661486	AG	--	27	GENIC	homozygous	48803852
14	78661930	78661931	C	T	25	GENIC	homozygous	48803853
14	78662227	78662228	A	G	19	GENIC	possibly homozygous	48803854
14	78662701	78662702	C	CT	27	GENIC	homozygous	48803855
14	78662705	78662706	T	TGTGCCTA	27	GENIC	homozygous	48803856
14	78664839	78664840	A	G	17	GENIC	homozygous	48803858
14	78665076	78665077	T	C	31	GENIC	homozygous	48803859