chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	38581646	38581647	A	-	5	GENIC	heterozygous	50194774
12	38585957	38585958	T	TAAA	7	GENIC	homozygous	50542254
12	38585929	38585930	G	GCTCT	4	GENIC	homozygous	50542252
12	38585930	38585931	A	ACCACT	4	GENIC	homozygous	50542253
12	38585958	38585959	T	TCCCCAA	7	GENIC	homozygous	50542255
12	38592108	38592109	T	-	9	GENIC	heterozygous	50542256
12	38592244	38592246	TG	--	10	GENIC	heterozygous	50542257
12	38595320	38595321	C	CTGG	5	GENIC	homozygous	50194780
12	38595323	38595324	C	CTTGA	5	GENIC	homozygous	50194782
12	38595325	38595326	C	CTCAG	5	GENIC	homozygous	50542258
12	38595329	38595330	C	CTCTGGAAACGCAAT	4	GENIC	homozygous	50542259
12	38598227	38598228	A	-	4	GENIC	heterozygous	50322790
12	38606776	38606777	G	GA	1	GENIC	homozygous	50542260
12	38606934	38606935	T	TGCGCGCGCGC	2	GENIC	homozygous	50542261
12	38608830	38608831	C	-	7	GENIC	homozygous	50194796
12	38619570	38619571	T	-	9	GENIC	heterozygous	50412772
12	38619831	38619833	TG	--	16	GENIC	heterozygous	50542262
12	38635090	38635091	G	GTT	3	GENIC	heterozygous	50542263
12	38583566	38583568	CA	--	19	GENIC	heterozygous	50542249
12	38585918	38585919	G	GCTTGCT	1	GENIC	homozygous	50542250
12	38585925	38585926	G	GCA	3	GENIC	homozygous	50542251