chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	63769999	63770000	A	G	14	GENIC	homozygous	68455281
9	63771844	63771845	G	A	19	GENIC	homozygous	68455284
9	63772700	63772701	A	G	32	GENIC	homozygous	68455287
9	63773136	63773137	C	T	244	GENIC	homozygous	68455290
9	63773855	63773856	A	G	40	GENIC	homozygous	68455292
9	63773945	63773946	T	G	41	GENIC	homozygous	68455295
9	63774478	63774479	T	C	41	GENIC	homozygous	68455298
9	63774965	63774966	T	G	22	GENIC	homozygous	68455301
9	63776665	63776666	C	T	13	GENIC	homozygous	68455304
9	63777143	63777144	T	A	41	GENIC	possibly homozygous	68455307
9	63777637	63777638	A	T	49	GENIC	heterozygous	68455310
9	63777777	63777778	G	A	36	GENIC	homozygous	68455313
9	63777781	63777782	A	G	35	GENIC	homozygous	68455316
9	63778487	63778488	G	A	43	GENIC	homozygous	68455319
9	63779248	63779249	G	T	31	GENIC	homozygous	68455322
9	63779550	63779551	A	G	27	GENIC	homozygous	68455324
9	63780214	63780215	A	G	25	GENIC	homozygous	68455327
9	63783049	63783050	A	C	21	GENIC	homozygous	68455330
9	63785545	63785546	A	G	22	GENIC	homozygous	68455332
9	63788094	63788095	G	A	53	GENIC	homozygous	68455335
9	63788249	63788250	T	A	23	GENIC	homozygous	68455338
9	63789753	63789754	A	G	21	GENIC	homozygous	68455341
9	63789798	63789799	G	A	23	GENIC	homozygous	68455344
9	63777631	63777632	T	A	49	GENIC	heterozygous	68620538