chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6053801	6053802	C	T	25	GENIC	homozygous	45673207
20	6055235	6055236	C	G	12	GENIC	homozygous	45391689
20	6055388	6055389	A	G	13	GENIC	homozygous	45391690
20	6055529	6055530	G	-	9	GENIC	homozygous	45673208
20	6055532	6055537	GTGCG	-----	11	GENIC	homozygous	45673209
20	6055536	6055537	G	-	11	GENIC	homozygous	45673210
20	6055717	6055718	A	-	17	GENIC	homozygous	45391694
20	6055727	6055728	A	G	21	GENIC	homozygous	45391696
20	6056047	6056048	G	A	31	GENIC	homozygous	45391699
20	6056158	6056159	G	GA	20	GENIC	homozygous	45391701
20	6056168	6056169	G	T	21	GENIC	homozygous	45391703
20	6056210	6056211	C	T	20	GENIC	homozygous	45391705
20	6056238	6056239	G	A	22	GENIC	homozygous	45391707
20	6056298	6056299	T	A	15	GENIC	homozygous	45391709
20	6056299	6056300	T	C	15	GENIC	homozygous	45391711
20	6056331	6056332	A	C	14	GENIC	homozygous	45391713
20	6056432	6056433	G	A	21	GENIC	heterozygous	45391715
20	6056438	6056439	C	CGGATCAGGGGCCAT	14	GENIC	homozygous	45391717
20	6056442	6056443	T	-	14	GENIC	heterozygous	45391719
20	6056447	6056448	A	G	16	GENIC	heterozygous	45391721
20	6056530	6056531	C	A	20	GENIC	homozygous	45391722
20	6056546	6056547	A	G	27	GENIC	homozygous	45391724
20	6056596	6056597	G	A	21	GENIC	homozygous	45391726
20	6056711	6056712	C	T	15	GENIC	homozygous	45391728
20	6057454	6057455	C	T	21	GENIC	homozygous	45391732
20	6057913	6057914	G	A	13	GENIC	homozygous	45391734