chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	55575798	55575799	C	T	70	GENIC	homozygous	116602605
10	55576276	55576277	A	T	71	GENIC	homozygous	116602607
10	55578017	55578018	A	G	57	GENIC	homozygous	116934871
10	55579072	55579073	C	T	56	GENIC	homozygous	116602609
10	55580020	55580020		AAGCAAAGCAACAT	65	GENIC	homozygous	128818963
10	55581194	55581195	T	C	30	GENIC	homozygous	117994770
10	55581417	55581418	A	C	48	GENIC	homozygous	116602611
10	55583055	55583056	T	C	61	GENIC	possibly homozygous	116602613
10	55583484	55583485	A	G	57	GENIC	homozygous	116602615
10	55584487	55584488	C	T	65	GENIC	homozygous	116602617
10	55584861	55585033	TAAGCTGCTGTCTCTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTTTTTTTTACTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCTTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC		42	GENIC	homozygous	128818964
10	55585184	55585184		GGGCGGGTAGTGAGTGT	28	GENIC	homozygous	128818965
10	55585200	55585201	A	G	32	GENIC	homozygous	116602619
10	55586307	55586308	G	A	28	GENIC	homozygous	116602621
10	55586612	55586613	A	G	48	GENIC	homozygous	116602623
10	55587635	55587636	T	C	46	GENIC	homozygous	116602625
10	55589499	55589499		GAG	61	GENIC	homozygous	128818966
10	55590430	55590431	C	T	37	GENIC	homozygous	116602627
10	55592744	55592759	TAATAATAATAATAT		37	GENIC	homozygous	128818967
10	55593366	55593367	C	A	50	GENIC	homozygous	116602631
10	55592052	55592053	T	A	51	GENIC	homozygous	116890216
10	55593013	55593014	C	T	40	GENIC	homozygous	116890218