chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	55572000	55572001	G	A	80	GENIC	homozygous	116782662
10	55572402	55572403	C	T	56	GENIC	homozygous	116782664
10	55572718	55572719	A	G	49	GENIC	homozygous	116782666
10	55572908	55572909	T		51	GENIC	homozygous	131094348
10	55573072	55573073	A	G	48	GENIC	homozygous	116934861
10	55576561	55576561		GA	51	GENIC	homozygous	131094350
10	55577097	55577098	G	A	71	GENIC	homozygous	116782668
10	55578017	55578018	A	G	70	GENIC	homozygous	116934871
10	55574976	55574977	T	A	59	GENIC	homozygous	116978011
10	55575798	55575799	C	T	51	GENIC	homozygous	116602605
10	55576276	55576277	A	T	67	GENIC	homozygous	116602607
10	55580859	55580860	C	T	61	GENIC	homozygous	116782670
10	55581417	55581418	A	C	51	GENIC	homozygous	116602611
10	55583055	55583056	T	C	54	GENIC	homozygous	116602613
10	55583484	55583485	A	G	51	GENIC	homozygous	116602615
10	55585200	55585201	A	G	38	GENIC	homozygous	116602619
10	55586307	55586308	G	A	39	GENIC	possibly homozygous	116602621
10	55586309	55586310	T	C	40	GENIC	possibly homozygous	126460701
10	55586612	55586613	A	G	53	GENIC	homozygous	116602623
10	55587635	55587636	T	C	65	GENIC	homozygous	116602625
10	55590430	55590431	C	T	37	GENIC	homozygous	116602627
10	55591042	55591043	T	A	42	GENIC	possibly homozygous	123444016
10	55591043	55591044	T	A	42	GENIC	homozygous	123444017
10	55592305	55592306	G		53	GENIC	homozygous	133229066
10	55580020	55580020		AAGCAAAGCAACAT	68	GENIC	homozygous	128818963
10	55584861	55585033	TAAGCTGCTGTCTCTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTTTTTTTTACTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCTTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC		54	GENIC	homozygous	128818964
10	55585184	55585184		GGGCGGGTAGTGAGTGT	27	GENIC	homozygous	128818965
10	55589499	55589499		GAG	55	GENIC	homozygous	128818966
10	55581194	55581195	T	C	48	GENIC	possibly homozygous	117994770
10	55590744	55590745	C	T	65	GENIC	homozygous	117011506