chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	101055537	101055538	G	GCC	29	GENIC	homozygous	55524181
6	101055554	101055556	GC	--	36	GENIC	homozygous	55419821
6	101056135	101056136	C	CTTT	7	GENIC	heterozygous	55524183
6	101055958	101055962	ACAG	----	41	GENIC	homozygous	54601814
6	101056135	101056136	C	CTTTT	7	GENIC	heterozygous	54601815
6	101056561	101056562	A	G	34	GENIC	homozygous	54601818
6	101056888	101056889	A	AT	32	GENIC	heterozygous	54601819
6	101056889	101056890	T	-	32	GENIC	possibly homozygous	54601820
6	101057505	101057506	G	A	49	GENIC	homozygous	54601821
6	101058413	101058414	A	-	22	GENIC	homozygous	54601822
6	101058901	101058902	T	G	34	GENIC	homozygous	54601824
6	101058958	101058959	T	TGAG	35	GENIC	homozygous	54601825
6	101059518	101059519	A	G	47	GENIC	homozygous	54601826
6	101059884	101059885	A	G	47	GENIC	homozygous	54601827
6	101060936	101060937	C	CT	21	GENIC	heterozygous	54601828
6	101061380	101061381	G	A	28	GENIC	homozygous	54601830
6	101061885	101061891	TTTGTT	------	10	GENIC	heterozygous	55524189
6	101062368	101062369	A	AT	15	GENIC	homozygous	54601831
6	101062423	101062435	GCACACCTCAGC	------------	15	GENIC	homozygous	54601832
6	101062947	101062948	T	A	19	GENIC	homozygous	54601833
6	101064349	101064350	T	A	38	GENIC	possibly homozygous	54601834
6	101065477	101065478	T	TACCTGAAAAA	16	GENIC	homozygous	54601836
6	101066118	101066119	G	GT	28	GENIC	possibly homozygous	54601837
6	101066831	101066832	A	G	51	GENIC	homozygous	54601838
6	101067142	101067143	C	T	27	GENIC	possibly homozygous	54601839
6	101067165	101067166	G	A	32	GENIC	possibly homozygous	54601840
6	101067168	101067169	G	C	31	GENIC	possibly homozygous	54601841
6	101067169	101067170	G	C	31	GENIC	possibly homozygous	54601842
6	101067296	101067297	A	C	36	GENIC	homozygous	54601846
6	101067419	101067426	TTTTTTT	-------	1	GENIC	homozygous	54601848