chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	48084270	48084271	T	TCAAGA	17	GENIC	homozygous	46150428
19	48084278	48084279	T	TCTCTCCATAACAGG	19	GENIC	homozygous	46150429
19	48084580	48084581	A	G	29	GENIC	homozygous	46150430
19	48084691	48084692	G	A	23	GENIC	homozygous	46150431
19	48084748	48084749	C	CTTTTT	3	GENIC	heterozygous	46565580
19	48084771	48084773	GC	--	12	GENIC	heterozygous	46407662
19	48084777	48084778	G	T	11	GENIC	homozygous	46150432
19	48084807	48084808	G	-	19	GENIC	homozygous	46150433
19	48084813	48084814	G	GTT	10	GENIC	homozygous	46150435
19	48084983	48084984	G	T	35	GENIC	homozygous	46150436
19	48085209	48085210	A	G	32	GENIC	homozygous	46150437
19	48085621	48085622	G	C	31	GENIC	homozygous	46150438
19	48085896	48085897	G	GAAA	3	GENIC	homozygous	46150439
19	48086071	48086072	C	CAAAAAAAAAA	10	GENIC	homozygous	46565582
19	48086149	48086150	A	C	26	GENIC	possibly homozygous	46150440
19	48086150	48086151	A	T	27	GENIC	possibly homozygous	46150441
19	48086481	48086482	G	C	14	GENIC	homozygous	46150442