chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	30584138	30584139	A	G	25	GENIC	homozygous	138754914
10	30584431	30584432	A	G	24	GENIC	homozygous	138754915
10	30584532	30584533	G	A	23	GENIC	homozygous	138754916
10	30585090	30585091	C	T	22	GENIC	homozygous	138754917
10	30585343	30585344	C	T	18	GENIC	homozygous	138754918
10	30587775	30587776	T	C	17	GENIC	homozygous	138754919
10	30588880	30588881	C	T	13	GENIC	homozygous	138754920
10	30589003	30589004	A	G	22	GENIC	homozygous	138754921
10	30589792	30589793	A	C	19	GENIC	homozygous	138754922
10	30591483	30591484	A	G	13	GENIC	homozygous	138754923
10	30593311	30593312	T	C	10	GENIC	homozygous	138754924
10	30596745	30596746	C	T	20	GENIC	homozygous	138754925
10	30597780	30597781	T	C	22	GENIC	homozygous	138754926
10	30598121	30598122	C	T	19	GENIC	homozygous	138754927
10	30598130	30598131	G	A	18	GENIC	homozygous	138754928
10	30598613	30598613		GGA	19	GENIC	homozygous	138676344
10	30598833	30598834	C	T	22	GENIC	homozygous	138754929
10	30599067	30599068	G	C	15	GENIC	homozygous	138754930
10	30599092	30599093	G	T	14	GENIC	homozygous	138754931
10	30599175	30599176	G	A	18	GENIC	homozygous	138754932
10	30599308	30599309	G	A	21	GENIC	homozygous	138754933
10	30599471	30599472	G	C	19	GENIC	homozygous	138754934
10	30599764	30599765	G		10	GENIC	possibly homozygous	403280997
10	30599764	30599765	G	A	10	GENIC	heterozygous	403280998
10	30599760	30599761	G		10	GENIC	possibly homozygous	403280995
10	30599760	30599761	G	C	10	GENIC	heterozygous	403280996
10	30599800	30599801	G	C	21	GENIC	homozygous	138754935
10	30599802	30599803	G	T	21	GENIC	homozygous	138754936
10	30600206	30600207	A	G	19	GENIC	homozygous	138754937