chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3995757	3995758	A	C	28	INTERGENIC	homozygous	45730052
20	3995774	3995775	A	G	24	INTERGENIC	homozygous	45374464
20	3996471	3996472	T	G	31	GENIC	possibly homozygous	45374466
20	3996830	3996831	C	G	35	GENIC	homozygous	45730053
20	3996859	3996860	G	GCA	28	GENIC	possibly homozygous	45730054
20	3997068	3997069	G	A	31	GENIC	homozygous	45730055
20	3997126	3997144	GTGTGTGTGTGTGTGTGT	------------------	10	GENIC	homozygous	45838315
20	3997873	3997874	A	AG	14	GENIC	possibly homozygous	45374473
20	3998001	3998002	T	TA	15	GENIC	heterozygous	45374474
20	3998443	3998444	G	A	36	GENIC	possibly homozygous	45730056
20	3998760	3998761	A	G	26	GENIC	homozygous	45374475
20	3999135	3999136	C	T	29	GENIC	homozygous	45730057
20	3999950	3999951	T	TA	33	GENIC	possibly homozygous	45730058
20	4004135	4004136	T	C	28	GENIC	homozygous	45374485
20	4004427	4004428	G	-	21	GENIC	homozygous	45374486
20	4004716	4004717	A	C	27	GENIC	homozygous	45971204
20	4004755	4004756	T	G	28	GENIC	homozygous	45374488
20	4004804	4004805	C	T	29	GENIC	homozygous	45971205
20	4005568	4005569	T	TACAC	4	GENIC	homozygous	45891145
20	4005626	4005627	T	-	23	GENIC	homozygous	45971206
20	4007276	4007277	G	A	20	GENIC	homozygous	45971207
20	4008973	4008974	G	A	4	GENIC	heterozygous	45818336
20	4009398	4009399	G	-	28	GENIC	possibly homozygous	45374500