chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39873850	39873851	T	C	13	GENIC	homozygous	50380988
12	39874777	39874778	A	G	15	GENIC	homozygous	50380989
12	39874992	39874993	G	A	32	GENIC	homozygous	50201973
12	39875037	39875039	GT	--	17	GENIC	homozygous	50201975
12	39875072	39875073	T	TGC	7	GENIC	homozygous	50380990
12	39875078	39875084	TGTGTA	------	4	GENIC	homozygous	50201977
12	39875331	39875332	G	GGTGTGTGTGT	16	GENIC	heterozygous	50655135
12	39875350	39875351	G	GTC	18	GENIC	homozygous	50201989
12	39875397	39875398	A	G	18	GENIC	homozygous	50201993
12	39875512	39875514	TA	--	19	GENIC	homozygous	50201997
12	39875989	39875991	AA	--	23	GENIC	heterozygous	50323165
12	39875990	39875991	A	-	23	GENIC	heterozygous	50202005
12	39876820	39876821	C	CTTTTTT	12	GENIC	homozygous	50380994
12	39876845	39876846	T	C	16	GENIC	homozygous	50380995
12	39877253	39877254	A	-	18	GENIC	homozygous	50380996
12	39877765	39877766	G	-	14	GENIC	homozygous	50512107
12	39878253	39878254	C	CAAAAAAAAAAAAA	8	GENIC	heterozygous	50563451
12	39878275	39878276	A	-	5	GENIC	homozygous	50202013
12	39878413	39878414	T	TACACAC	5	GENIC	homozygous	50604468
12	39878604	39878611	AAAAAAA	-------	12	GENIC	homozygous	50571479
12	39879271	39879272	T	G	12	GENIC	homozygous	50380997
12	39879495	39879496	A	G	22	GENIC	homozygous	50202023
12	39879913	39879914	T	C	18	GENIC	homozygous	50380998
12	39880710	39880711	C	-	16	GENIC	homozygous	50202027
12	39881481	39881482	C	G	29	GENIC	homozygous	50202030
12	39881764	39881765	G	A	27	GENIC	homozygous	50380999