chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	15379677	15379678	C	T	45	GENIC	homozygous	117267684
9	15379789	15379790	A	G	28	GENIC	homozygous	117267685
9	15380347	15380348	G	A	36	GENIC	homozygous	117267686
9	15380881	15380882	T	C	37	GENIC	homozygous	117267687
9	15381078	15381079	C	G	38	GENIC	homozygous	117267688
9	15381622	15381623	A	G	33	GENIC	homozygous	117267689
9	15382500	15382501	C	T	13	GENIC	homozygous	117267690
9	15382584	15382585	A	G	17	GENIC	homozygous	117267691
9	15382591	15382592	T	C	19	GENIC	homozygous	117267692
9	15383418	15383419	G	A	39	GENIC	homozygous	117267693
9	15384516	15384517	T	G	31	GENIC	homozygous	117267696
9	15384919	15384920	A	C	20	GENIC	homozygous	117267698
9	15384991	15384992	T	C	23	GENIC	homozygous	117460976
9	15384992	15384993	G	T	23	GENIC	homozygous	117460977
9	15385694	15385695	G	A	20	GENIC	homozygous	117267701
9	15386128	15386129	C	A	37	GENIC	homozygous	117267704
9	15386153	15386154	T	C	46	GENIC	homozygous	117267705
9	15386645	15386646	C	T	27	GENIC	homozygous	117267706
9	15387240	15387241	T	C	26	GENIC	homozygous	117267707
9	15390204	15390205	A	G	37	GENIC	homozygous	117267713
9	15390605	15390606	T	C	35	GENIC	homozygous	117267714
9	15391019	15391020	C	T	26	GENIC	homozygous	117267715
9	15391445	15391446	T	C	35	GENIC	homozygous	117267716