chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3618991	3618991		ATGGG	20	GENIC	homozygous	129978312
20	3619023	3619024	G	T	19	GENIC	homozygous	142722790
20	3619048	3619049	G	A	16	GENIC	homozygous	142722791
20	3619054	3619054		GTCA	9	GENIC	possibly homozygous	129978313
20	3619808	3619809	A	G	23	GENIC	homozygous	142722792
20	3619816	3619817	A	C	27	GENIC	possibly homozygous	142722793
20	3619915	3619916	C	T	26	GENIC	homozygous	142722794
20	3620316	3620317	T	C	22	GENIC	possibly homozygous	142722795
20	3620397	3620398	A	G	16	GENIC	homozygous	142722796
20	3620400	3620401	A	G	14	GENIC	homozygous	142722797
20	3620401	3620402	T	C	14	GENIC	homozygous	142722798
20	3620415	3620416	G	A	15	GENIC	homozygous	142722799
20	3619675	3619675		C	19	GENIC	homozygous	142711819
20	3619807	3619807		GG	23	GENIC	homozygous	142711820
20	3620546	3620547	G	A	22	GENIC	homozygous	142722800
20	3620464	3620465	T	C	22	GENIC	homozygous	130025298
20	3620928	3620929	G	A	22	GENIC	homozygous	142722801
20	3620955	3620956	A	G	23	GENIC	homozygous	142722802
20	3621000	3621001	T	A	15	GENIC	homozygous	142722803
20	3621007	3621008	A	G	15	GENIC	homozygous	142722804