chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	47943277	47943278	A	G	11	GENIC	possibly homozygous	46030616
20	47943574	47943575	A	G	28	GENIC	possibly homozygous	45643635
20	47943583	47943584	A	AC	26	GENIC	possibly homozygous	46030617
20	47943833	47943834	G	A	21	GENIC	homozygous	46030618
20	47943859	47943860	T	-	15	GENIC	homozygous	45643637
20	47943878	47943879	A	-	20	GENIC	homozygous	46032090
20	47945038	47945039	G	A	22	GENIC	homozygous	46030619
20	47945199	47945200	T	-	22	GENIC	possibly homozygous	46016092
20	47945684	47945685	T	C	28	GENIC	possibly homozygous	46030620
20	47945879	47945886	AACTGTT	-------	28	GENIC	possibly homozygous	46030621
20	47946155	47946156	G	GT	26	GENIC	possibly homozygous	45643642
20	47946715	47946716	G	A	22	GENIC	homozygous	45643645
20	47947486	47947494	AAGGCCTG	--------	32	GENIC	possibly homozygous	46030622
20	47947498	47947499	C	T	33	GENIC	possibly homozygous	46030623
20	47947931	47947932	A	T	30	GENIC	homozygous	45875165
20	47947932	47947933	T	C	30	GENIC	homozygous	45875166
20	47948038	47948039	T	G	34	GENIC	homozygous	45643649
20	47948195	47948196	A	C	44	GENIC	possibly homozygous	46030624
20	47948655	47948656	G	A	30	GENIC	homozygous	46030625
20	47948880	47948881	A	G	32	GENIC	possibly homozygous	46030626
20	47949550	47949551	A	G	16	GENIC	possibly homozygous	46016103
20	47949771	47949772	T	-	14	GENIC	possibly homozygous	45891854
20	47950378	47950379	C	T	30	GENIC	homozygous	46030627
20	47950954	47950955	A	ATATTT	29	GENIC	possibly homozygous	45643651