chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	130476924	130476925	T	C	18	GENIC	homozygous	143330567
6	130477773	130477774	G	A	23	GENIC	homozygous	146170885
6	130478068	130478069	G	A	14	GENIC	homozygous	143330568
6	130478156	130478157	T	C	18	GENIC	homozygous	146170886
6	130479926	130479927	C	T	19	GENIC	homozygous	143330570
6	130480523	130480524	C	G	16	GENIC	homozygous	146170887
6	130477897	130477898	G		17	GENIC	homozygous	143280365
6	130478209	130478210	A	G	27	GENIC	homozygous	137912029
6	130481444	130481445	A	G	26	GENIC	homozygous	137912032
6	130481550	130481551	T	A	19	GENIC	homozygous	137912034
6	130482726	130482727	G	T	18	GENIC	homozygous	137912035
6	130482865	130482866	C	T	35	GENIC	homozygous	146170888
6	130482988	130482989	C	A	24	GENIC	possibly homozygous	137912036
6	130483323	130483324	T	A	16	GENIC	homozygous	137912037
6	130484455	130484456	G	A	21	GENIC	homozygous	146170889
6	130485032	130485033	G	A	29	GENIC	homozygous	146170890
6	130485518	130485519	T	C	26	GENIC	homozygous	137912038
6	130486464	130486465	C	T	17	GENIC	homozygous	146170891
6	130488210	130488211	T	C	20	GENIC	homozygous	146170892
6	130488212	130488213	T	C	20	GENIC	homozygous	146170893
6	130483175	130483175		C	24	GENIC	homozygous	137711125
6	130489871	130489873	AT		14	GENIC	possibly homozygous	137711126