chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4044149	4044150	G	A	10	INTERGENIC	possibly homozygous	45730104
20	4044378	4044379	T	C	11	INTERGENIC	possibly homozygous	45730105
20	4044544	4044545	A	T	17	INTERGENIC	possibly homozygous	45374644
20	4044834	4044835	T	C	12	GENIC	homozygous	45374645
20	4045193	4045194	G	A	7	GENIC	homozygous	45730106
20	4045837	4045838	G	A	9	GENIC	homozygous	45730107
20	4046229	4046230	G	A	6	GENIC	homozygous	45730108
20	4046230	4046231	C	A	5	GENIC	homozygous	45730109
20	4046299	4046300	C	A	11	GENIC	heterozygous	45730110
20	4046317	4046318	A	ACC	2	GENIC	homozygous	45374654
20	4046573	4046575	TT	--	2	GENIC	homozygous	45374657
20	4047190	4047191	A	G	14	GENIC	homozygous	45730111
20	4047385	4047386	G	GATAC	1	GENIC	homozygous	45818340
20	4047598	4047599	C	A	12	GENIC	homozygous	45374663
20	4047620	4047626	ACACAC	------	4	GENIC	homozygous	45374664
20	4047725	4047726	T	C	3	GENIC	heterozygous	45374666
20	4047933	4047934	C	G	7	GENIC	homozygous	45374681
20	4048031	4048032	A	C	17	GENIC	heterozygous	45374682
20	4048469	4048470	A	G	2	GENIC	homozygous	45374685
20	4048562	4048563	T	TGTGCG	6	GENIC	homozygous	45374686
20	4049223	4049225	AC	--	6	GENIC	homozygous	45374687