chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5388821	5388822	A	G	24	GENIC	homozygous	45386510
20	5389655	5389656	G	A	31	GENIC	homozygous	45386519
20	5389773	5389774	C	G	30	GENIC	homozygous	45386521
20	5390225	5390226	T	TGGTCTCCCTGCCTACAGTTGTGGCCCCA	31	GENIC	homozygous	45818522
20	5391305	5391306	T	C	39	GENIC	homozygous	45386536
20	5391411	5391412	C	T	40	GENIC	homozygous	45731706
20	5391604	5391605	C	-	41	GENIC	homozygous	45731707
20	5391828	5391829	T	C	35	GENIC	possibly homozygous	45731708
20	5391836	5391837	A	G	36	GENIC	possibly homozygous	45386542
20	5392767	5392768	C	A	30	GENIC	homozygous	45386547
20	5394467	5394472	ACACA	-----	12	GENIC	homozygous	45731710
20	5394476	5394477	T	-	9	GENIC	homozygous	45386559
20	5395187	5395188	A	-	27	GENIC	homozygous	45752710
20	5390392	5390393	C	CACTTTCTTTCTGTCCGAGTAAGACACCTGCACAG	21	GENIC	homozygous	45862082
20	5394509	5394510	A	AC	4	GENIC	homozygous	45862084
20	5394512	5394513	C	CA	4	GENIC	homozygous	45862085
20	5394516	5394517	A	AC	4	GENIC	homozygous	45862086
20	5394055	5394056	G	A	26	GENIC	homozygous	45752707
20	5394479	5394480	T	-	9	GENIC	homozygous	45971865
20	5395331	5395332	T	A	28	GENIC	homozygous	45386561
20	5395782	5395783	G	A	35	GENIC	homozygous	45386563
20	5395949	5395950	A	G	26	GENIC	possibly homozygous	45386565
20	5396546	5396547	T	C	39	GENIC	homozygous	45386569