chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	15269408	15269408		GAAG	31	GENIC	possibly homozygous	128683165
9	15269499	15269499		GG	18	GENIC	homozygous	128683166
9	15269609	15269610	G		32	GENIC	homozygous	128683167
9	15270645	15270650	AAAAT		54	GENIC	homozygous	128683169
9	15272218	15272219	A	G	47	GENIC	homozygous	117267492
9	15270764	15270765	C	T	36	GENIC	homozygous	117267489
9	15271104	15271105	T	C	55	GENIC	homozygous	117267490
9	15271904	15271905	A	G	60	GENIC	homozygous	117267491
9	15272231	15272232	C	T	47	GENIC	homozygous	117267493
9	15272338	15272339	A	G	60	GENIC	homozygous	117267494
9	15273460	15273461	T	C	41	GENIC	homozygous	117267496
9	15273599	15273600	C	T	52	GENIC	homozygous	117267497
9	15273964	15273965	T	C	52	GENIC	homozygous	117267498
9	15273979	15273980	A	G	51	GENIC	homozygous	117267499
9	15274134	15274135	A	C	44	GENIC	homozygous	117267500
9	15274443	15274444	T	C	50	GENIC	homozygous	117267501
9	15274481	15274482	G	C	53	GENIC	homozygous	117267502
9	15274587	15274588	G	A	38	GENIC	homozygous	117267503
9	15274868	15274869	T	C	52	GENIC	homozygous	117267504