chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3990826	3990827	C	G	7	GENIC	homozygous	109070773
20	3990855	3990856	C	A	6	GENIC	homozygous	109070775
20	3991058	3991059	C	T	10	GENIC	homozygous	109070777
20	3991065	3991066	T	G	9	GENIC	homozygous	109070779
20	3991087	3991088	T	G	9	GENIC	homozygous	109070781
20	3991120	3991121	C	G	8	GENIC	homozygous	109070783
20	3991123	3991124	A	G	8	GENIC	homozygous	109070785
20	3991161	3991162	T	C	10	GENIC	homozygous	109070787
20	3991170	3991171	T	G	8	GENIC	homozygous	109070789
20	3991293	3991294	G	A	11	GENIC	homozygous	109070791
20	3991316	3991317	G	C	11	GENIC	homozygous	109070793
20	3991346	3991347	T	C	13	GENIC	homozygous	109070795
20	3991349	3991350	A	G	13	GENIC	homozygous	109070797
20	3991427	3991428	C	T	13	GENIC	homozygous	109070799
20	3991430	3991431	C	T	12	GENIC	homozygous	109070801
20	3991450	3991451	C	T	13	GENIC	homozygous	109070803
20	3991516	3991517	A	T	17	GENIC	homozygous	109070805
20	3991615	3991616	G	A	12	GENIC	homozygous	109070807
20	3991628	3991629	C	T	11	GENIC	possibly homozygous	109070809
20	3991666	3991667	T	C	11	GENIC	homozygous	109070811
20	3991667	3991668	C	T	11	GENIC	homozygous	109070813
20	3991695	3991696	A	G	12	GENIC	homozygous	109070815
20	3991746	3991747	C	T	17	GENIC	homozygous	109070817
20	3991770	3991771	G	A	17	GENIC	homozygous	109070819
20	3991794	3991795	G	T	14	GENIC	homozygous	109070821
20	3991797	3991798	G	A	12	GENIC	homozygous	109070823
20	3991922	3991923	T	G	11	GENIC	homozygous	109070831
20	3991982	3991983	C	T	18	GENIC	homozygous	109294854
20	3992009	3992010	C	T	16	GENIC	homozygous	109070833
20	3992093	3992094	T	G	6	GENIC	homozygous	109294856
20	3992096	3992097	T	C	5	GENIC	homozygous	109070835
20	3992102	3992103	T	C	6	GENIC	homozygous	109070837
20	3992134	3992135	T	C	6	GENIC	homozygous	109070841