chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	124124721	124124722	T	TGGTATGGTAA	14	GENIC	possibly homozygous	55535909
6	124124778	124124779	G	GT	22	GENIC	homozygous	54687102
6	124125125	124125126	A	G	24	GENIC	homozygous	54687103
6	124127497	124127498	G	A	36	GENIC	homozygous	54687104
6	124128152	124128153	C	T	47	GENIC	homozygous	54687105
6	124128216	124128217	T	C	38	GENIC	homozygous	54687106
6	124130484	124130485	A	G	39	GENIC	homozygous	54687107
6	124130660	124130661	C	A	32	GENIC	homozygous	54687108
6	124130855	124130856	T	C	37	GENIC	homozygous	54687109
6	124132452	124132453	T	TG	20	GENIC	homozygous	54687110
6	124132455	124132456	G	A	20	GENIC	homozygous	54687111
6	124132457	124132458	T	C	21	GENIC	homozygous	54687112
6	124132458	124132459	T	A	20	GENIC	homozygous	54687113
6	124132460	124132461	G	GC	19	GENIC	homozygous	54687114
6	124132500	124132501	C	T	24	GENIC	homozygous	54687115
6	124133010	124133011	C	CTTT	14	GENIC	homozygous	54687116
6	124133736	124133737	T	C	14	GENIC	homozygous	54687117
6	124133981	124133982	T	C	27	GENIC	homozygous	54687118
6	124134364	124134368	GTGC	----	8	GENIC	heterozygous	54687120
6	124134406	124134407	G	A	17	GENIC	homozygous	54687122