chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4089081	4089082	C	T	17	GENIC	heterozygous	46027375
20	4089113	4089114	A	ATT	11	GENIC	heterozygous	46027376
20	4089421	4089422	T	C	14	GENIC	homozygous	45374822
20	4089437	4089438	A	G	19	GENIC	homozygous	45374823
20	4089483	4089484	C	T	22	GENIC	heterozygous	45374825
20	4091137	4091138	A	AT	11	INTERGENIC	homozygous	45374828
20	4091400	4091401	T	C	11	INTERGENIC	homozygous	45374830
20	4092600	4092601	A	G	22	INTERGENIC	homozygous	45374831
20	4093893	4093894	A	G	8	INTERGENIC	homozygous	45374833
20	4093986	4093987	G	GATTT	9	INTERGENIC	homozygous	45374835
20	4094339	4094340	C	T	11	INTERGENIC	homozygous	45374836
20	4094359	4094360	G	T	11	INTERGENIC	homozygous	45374838
20	4095136	4095137	T	C	13	INTERGENIC	homozygous	45374844
20	4096400	4096401	A	G	17	INTERGENIC	heterozygous	45374847
20	4097170	4097171	T	-	12	INTERGENIC	homozygous	45374849
20	4090425	4090426	C	-	8	GENIC	heterozygous	46035623
20	4095912	4095913	T	C	15	INTERGENIC	homozygous	46035627