chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	93029847	93029848	G	T	32	GENIC	homozygous	117388305
9	93031735	93031736	G	T	32	GENIC	possibly homozygous	117388306
9	93032069	93032070	G	A	59	GENIC	homozygous	117388307
9	93035650	93035651	A	G	18	GENIC	homozygous	117388308
9	93035660	93035661	A	G	18	GENIC	homozygous	117388309
9	93035803	93035804	A	G	59	GENIC	homozygous	117388310
9	93035891	93035892	G	A	58	GENIC	homozygous	117388311
9	93036254	93036255	G	A	68	GENIC	homozygous	117388312
9	93036616	93036617	T	C	52	GENIC	homozygous	117388313
9	93036882	93036883	C	T	58	GENIC	homozygous	117388314
9	93039278	93039279	T	C	39	GENIC	homozygous	117388315
9	93039937	93039938	C	T	35	GENIC	homozygous	117388316
9	93039938	93039939	A	G	34	GENIC	homozygous	117388317
9	93040670	93040671	G	A	44	GENIC	homozygous	117388318
9	93041082	93041083	C	A	32	GENIC	homozygous	117388319
9	93041176	93041177	G	T	26	GENIC	homozygous	117388320
9	93041433	93041434	T	C	24	GENIC	homozygous	117388321