chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	7394536	7394537	T	C	9	GENIC	heterozygous	45676740
20	7394554	7394564	CCTGAAGTTT	----------	9	GENIC	heterozygous	46044583
20	7394573	7394574	C	G	10	GENIC	heterozygous	46044585
20	7394644	7394645	T	C	5	GENIC	homozygous	45410361
20	7394659	7394660	G	A	11	GENIC	heterozygous	45410362
20	7394700	7394701	G	C	19	GENIC	heterozygous	46044587
20	7394707	7394708	C	G	19	GENIC	heterozygous	46044589
20	7394712	7394713	A	T	20	GENIC	heterozygous	46044591
20	7394728	7394729	C	G	27	GENIC	heterozygous	45621923
20	7394741	7394742	T	A	30	GENIC	heterozygous	45621924
20	7394744	7394745	C	A	28	GENIC	heterozygous	45621925
20	7394747	7394748	C	T	28	GENIC	heterozygous	45410364
20	7394765	7394766	A	G	39	GENIC	heterozygous	45736319
20	7394789	7394790	A	G	56	GENIC	heterozygous	45776592
20	7394841	7394842	G	C	48	GENIC	heterozygous	45736320
20	7394842	7394843	G	A	46	GENIC	heterozygous	45410365
20	7394843	7394844	C	T	47	GENIC	heterozygous	45736321
20	7394864	7394865	A	G	33	GENIC	heterozygous	45410367
20	7394870	7394871	G	A	32	GENIC	heterozygous	46044593
20	7394876	7394877	T	C	28	GENIC	heterozygous	45410368
20	7394894	7394898	ACCC	----	21	GENIC	heterozygous	46044595
20	7395045	7395046	G	C	14	GENIC	heterozygous	45410378
20	7395053	7395054	G	A	16	GENIC	heterozygous	45410380
20	7395057	7395058	T	G	17	GENIC	heterozygous	45410381
20	7395102	7395103	G	A	37	GENIC	heterozygous	45410384
20	7395109	7395110	A	G	37	GENIC	heterozygous	45410385
20	7395113	7395114	T	A	39	GENIC	heterozygous	45410386
20	7395141	7395142	C	T	47	GENIC	heterozygous	45410388
20	7395150	7395151	G	T	45	GENIC	heterozygous	45410389
20	7395158	7395159	C	T	43	GENIC	heterozygous	45410390
20	7395249	7395250	C	G	10	GENIC	homozygous	45410393
20	7395117	7395118	A	T	40	GENIC	heterozygous	46072010
20	7395071	7395072	C	A	26	GENIC	heterozygous	46072008