chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6053801	6053802	C	T	9	GENIC	homozygous	45673207
20	6055235	6055236	C	G	18	GENIC	homozygous	45391689
20	6055388	6055389	A	G	30	GENIC	homozygous	45391690
20	6055529	6055530	G	-	10	GENIC	homozygous	45673208
20	6055532	6055537	GTGCG	-----	13	GENIC	homozygous	45673209
20	6055717	6055718	A	-	28	GENIC	homozygous	45391694
20	6055727	6055728	A	G	29	GENIC	homozygous	45391696
20	6055924	6055925	T	-	28	GENIC	homozygous	45733005
20	6056047	6056048	G	A	14	GENIC	homozygous	45391699
20	6056158	6056159	G	GA	30	GENIC	homozygous	45391701
20	6056168	6056169	G	T	31	GENIC	homozygous	45391703
20	6056210	6056211	C	T	28	GENIC	homozygous	45391705
20	6056238	6056239	G	A	24	GENIC	homozygous	45391707
20	6056298	6056299	T	A	21	GENIC	homozygous	45391709
20	6056299	6056300	T	C	20	GENIC	homozygous	45391711
20	6056331	6056332	A	C	18	GENIC	homozygous	45391713
20	6056432	6056433	G	A	22	GENIC	homozygous	45391715
20	6056523	6056525	CG	--	27	GENIC	homozygous	45839690
20	6056525	6056526	T	TAC	27	GENIC	homozygous	45839691
20	6056530	6056531	C	A	28	GENIC	homozygous	45391722
20	6056546	6056547	A	G	22	GENIC	homozygous	45391724
20	6056596	6056597	G	A	16	GENIC	homozygous	45391726
20	6056711	6056712	C	T	11	GENIC	homozygous	45391728
20	6057454	6057455	C	T	22	GENIC	possibly homozygous	45391732
20	6057913	6057914	G	A	23	GENIC	homozygous	45391734