chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4044149	4044150	G	A	28	INTERGENIC	possibly homozygous	45730104
20	4044378	4044379	T	C	24	INTERGENIC	homozygous	45730105
20	4044544	4044545	A	T	17	INTERGENIC	homozygous	45374644
20	4044834	4044835	T	C	21	GENIC	homozygous	45374645
20	4045193	4045194	G	A	28	GENIC	homozygous	45730106
20	4045837	4045838	G	A	29	GENIC	homozygous	45730107
20	4046229	4046230	G	A	25	GENIC	homozygous	45730108
20	4046230	4046231	C	A	26	GENIC	homozygous	45730109
20	4046299	4046300	C	A	19	GENIC	homozygous	45730110
20	4046317	4046318	A	ACC	15	GENIC	homozygous	45374654
20	4046324	4046325	C	CACACACACAG	11	GENIC	heterozygous	45838347
20	4046324	4046325	C	CACACACACACAG	11	GENIC	possibly homozygous	45838348
20	4046573	4046575	TT	--	18	GENIC	homozygous	45374657
20	4047190	4047191	A	G	23	GENIC	homozygous	45730111
20	4047385	4047386	G	GATAC	6	GENIC	homozygous	45818340
20	4047619	4047624	TACAC	-----	8	GENIC	possibly homozygous	46027328
20	4047649	4047650	C	CATATATAT	11	GENIC	possibly homozygous	46027329
20	4047650	4047652	AT	--	11	GENIC	heterozygous	45374665
20	4047725	4047726	T	C	5	GENIC	homozygous	45374666
20	4048117	4048118	C	CCAAACCAAACCA	8	GENIC	homozygous	46027330
20	4048469	4048470	A	G	14	GENIC	homozygous	45374685
20	4048562	4048563	T	TGTGCG	24	GENIC	heterozygous	45374686
20	4048912	4048913	G	GTTTTTTTTTT	3	GENIC	homozygous	45838358
20	4049117	4049118	T	TA	10	GENIC	possibly homozygous	46027331