chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3995757	3995758	A	C	26	INTERGENIC	homozygous	45730052
20	3995774	3995775	A	G	31	INTERGENIC	homozygous	45374464
20	3996471	3996472	T	G	17	GENIC	homozygous	45374466
20	3996830	3996831	C	G	26	GENIC	homozygous	45730053
20	3996859	3996860	G	GCA	14	GENIC	possibly homozygous	45730054
20	3997068	3997069	G	A	33	GENIC	homozygous	45730055
20	3997124	3997144	GTGTGTGTGTGTGTGTGTGT	--------------------	5	GENIC	heterozygous	45838313
20	3997126	3997144	GTGTGTGTGTGTGTGTGT	------------------	5	GENIC	heterozygous	45838315
20	3997873	3997874	A	AG	3	GENIC	homozygous	45374473
20	3998001	3998002	T	TA	11	GENIC	possibly homozygous	45374474
20	3998443	3998444	G	A	15	GENIC	homozygous	45730056
20	3998760	3998761	A	G	33	GENIC	homozygous	45374475
20	3999135	3999136	C	T	27	GENIC	homozygous	45730057
20	3999950	3999951	T	TA	19	GENIC	possibly homozygous	45730058
20	4004135	4004136	T	C	18	GENIC	homozygous	45374485
20	4004427	4004428	G	-	11	GENIC	possibly homozygous	45374486
20	4004755	4004756	T	G	14	GENIC	homozygous	45374488
20	4009398	4009399	G	-	14	GENIC	homozygous	45374500
20	4008973	4008974	G	A	5	GENIC	homozygous	45818336
20	4004716	4004717	A	C	23	GENIC	homozygous	45971204
20	4004804	4004805	C	T	17	GENIC	homozygous	45971205
20	4005626	4005627	T	-	18	GENIC	homozygous	45971206
20	4007276	4007277	G	A	32	GENIC	homozygous	45971207