chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	78647727	78647728	T	C	16	GENIC	possibly homozygous	48803837
14	78648094	78648095	G	A	9	GENIC	homozygous	49519204
14	78649698	78649699	G	A	5	GENIC	heterozygous	48803838
14	78650159	78650160	A	G	6	GENIC	homozygous	48803839
14	78651400	78651401	A	G	17	GENIC	homozygous	48803840
14	78651807	78651808	G	A	13	GENIC	homozygous	48803841
14	78652817	78652818	A	G	11	GENIC	homozygous	48803842
14	78654123	78654124	T	C	6	GENIC	heterozygous	49519206
14	78654773	78654774	A	G	24	GENIC	homozygous	49343289
14	78655044	78655045	G	A	9	GENIC	possibly homozygous	49519208
14	78655934	78655935	G	-	3	GENIC	homozygous	49368428
14	78657289	78657290	T	C	16	GENIC	homozygous	48803845
14	78658359	78658360	T	TG	8	GENIC	possibly homozygous	49292012
14	78659263	78659264	A	G	16	GENIC	possibly homozygous	49343292
14	78659581	78659582	C	T	16	GENIC	possibly homozygous	49571940
14	78659979	78659980	T	C	8	GENIC	homozygous	49343294
14	78660207	78660208	G	A	2	GENIC	homozygous	49343295
14	78660398	78660399	G	A	14	GENIC	homozygous	49343296
14	78661083	78661084	G	A	14	GENIC	homozygous	49519214
14	78661484	78661486	AG	--	11	GENIC	homozygous	48803852
14	78661758	78661759	C	T	5	GENIC	homozygous	49343299
14	78662172	78662173	T	C	8	GENIC	homozygous	49343300
14	78662755	78662756	T	TAAAC	2	GENIC	homozygous	49519216
14	78663380	78663381	T	C	14	GENIC	possibly homozygous	49519218
14	78663502	78663503	C	A	11	GENIC	homozygous	49343304
14	78665743	78665744	G	T	15	GENIC	homozygous	48803861
14	78665886	78665887	A	G	8	GENIC	homozygous	49519220
14	78667051	78667052	A	C	19	GENIC	homozygous	48803864
14	78667901	78667902	A	G	9	GENIC	homozygous	48803870
14	78668371	78668372	A	G	11	GENIC	homozygous	49519222
14	78668909	78668910	C	T	12	GENIC	homozygous	48803875
14	78671481	78671482	A	G	9	GENIC	possibly homozygous	49519228
14	78671619	78671620	G	GT	20	GENIC	possibly homozygous	48803883
14	78672580	78672582	CC	--	8	GENIC	possibly homozygous	48803893