chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6633485	6633486	A		14	GENIC	homozygous	140483920
20	6633658	6633659	C	A	17	GENIC	homozygous	130037575
20	6633728	6633729	C	T	31	GENIC	homozygous	140512719
20	6633784	6633785	G	A	30	GENIC	homozygous	140512720
20	6633855	6633856	C	G	27	GENIC	homozygous	130037576
20	6634832	6634832		T	18	GENIC	homozygous	140483921
20	6635677	6635678	A	G	16	GENIC	homozygous	130037579
20	6635826	6635827	T	C	15	GENIC	homozygous	130037580
20	6637045	6637046	A	T	15	GENIC	homozygous	130037581
20	6634144	6634148	GGGT		16	GENIC	homozygous	129980651
20	6636638	6636638		GACAT	10	GENIC	homozygous	129980653
20	6637919	6637920	T	C	17	GENIC	homozygous	130037582
20	6637982	6637983	T	C	16	GENIC	homozygous	130037583
20	6638319	6638320	A	G	15	GENIC	homozygous	130037585
20	6638510	6638511	G	C	3	GENIC	homozygous	140512721
20	6639093	6639093		A	14	GENIC	homozygous	140483922
20	6639109	6639114	AAAAG		14	GENIC	homozygous	140483923
20	6639258	6639259	C	G	13	GENIC	homozygous	130037588
20	6639112	6639113	A	G	14	GENIC	heterozygous	404039770
20	6639282	6639283	G	A	14	GENIC	homozygous	155133250
20	6639113	6639114	G	A	14	GENIC	heterozygous	155133249
20	6639112	6639113	A		14	GENIC	homozygous	404039769
20	6639113	6639114	G		14	GENIC	homozygous	404039771
20	6641035	6641035		TCC	7	GENIC	homozygous	140483925
20	6641146	6641147	A	G	12	GENIC	homozygous	130037592
20	6641724	6641725	A	C	16	GENIC	homozygous	130037594
20	6641875	6641876	T	C	27	GENIC	homozygous	130037595