chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	15379677	15379678	C	T	21	GENIC	homozygous	117267684
9	15379789	15379790	A	G	10	GENIC	homozygous	117267685
9	15380347	15380348	G	A	24	GENIC	homozygous	117267686
9	15380881	15380882	T	C	16	GENIC	homozygous	117267687
9	15381078	15381079	C	G	21	GENIC	homozygous	117267688
9	15381622	15381623	A	G	24	GENIC	homozygous	117267689
9	15382500	15382501	C	T	21	GENIC	homozygous	117267690
9	15382584	15382585	A	G	17	GENIC	homozygous	117267691
9	15382591	15382592	T	C	21	GENIC	homozygous	117267692
9	15383418	15383419	G	A	29	GENIC	homozygous	117267693
9	15384219	15384220	A	G	25	GENIC	homozygous	117267695
9	15384516	15384517	T	G	19	GENIC	homozygous	117267696
9	15384919	15384920	A	C	25	GENIC	homozygous	117267698
9	15384991	15384992	T	C	18	GENIC	homozygous	117460976
9	15384992	15384993	G	T	18	GENIC	homozygous	117460977
9	15385694	15385695	G	A	25	GENIC	homozygous	117267701
9	15386128	15386129	C	A	19	GENIC	homozygous	117267704
9	15386153	15386154	T	C	18	GENIC	homozygous	117267705
9	15386645	15386646	C	T	16	GENIC	homozygous	117267706
9	15390204	15390205	A	G	22	GENIC	homozygous	117267713
9	15390605	15390606	T	C	22	GENIC	homozygous	117267714
9	15391019	15391020	C	T	18	GENIC	homozygous	117267715
9	15391445	15391446	T	C	12	GENIC	homozygous	117267716