chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	124124721	124124722	T	A	31	GENIC	heterozygous	54687099
6	124124731	124124732	T	A	34	GENIC	heterozygous	54687100
6	124124757	124124758	A	G	28	GENIC	homozygous	54687101
6	124124778	124124779	G	GT	26	GENIC	homozygous	54687102
6	124125125	124125126	A	G	32	GENIC	homozygous	54687103
6	124127497	124127498	G	A	38	GENIC	homozygous	54687104
6	124128152	124128153	C	T	52	GENIC	homozygous	54687105
6	124128216	124128217	T	C	51	GENIC	homozygous	54687106
6	124130484	124130485	A	G	44	GENIC	homozygous	54687107
6	124130660	124130661	C	A	36	GENIC	homozygous	54687108
6	124130855	124130856	T	C	46	GENIC	homozygous	54687109
6	124132452	124132453	T	TG	15	GENIC	homozygous	54687110
6	124132455	124132456	G	A	14	GENIC	homozygous	54687111
6	124132457	124132458	T	C	13	GENIC	homozygous	54687112
6	124132458	124132459	T	A	13	GENIC	homozygous	54687113
6	124132460	124132461	G	GC	12	GENIC	homozygous	54687114
6	124132500	124132501	C	T	17	GENIC	homozygous	54687115
6	124133010	124133011	C	CTTT	8	GENIC	homozygous	54687116
6	124133736	124133737	T	C	17	GENIC	homozygous	54687117
6	124133981	124133982	T	C	31	GENIC	possibly homozygous	54687118
6	124134360	124134361	G	T	30	GENIC	heterozygous	54687119
6	124134364	124134368	GTGC	----	25	GENIC	heterozygous	54687120
6	124134404	124134405	G	A	25	GENIC	heterozygous	54687121
6	124134406	124134407	G	A	25	GENIC	heterozygous	54687122