chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4022198	4022199	C	A	20	GENIC	homozygous	63662059
20	4024415	4024416	C	T	17	GENIC	homozygous	63662060
20	4025237	4025238	A	G	9	GENIC	homozygous	63335520
20	4025293	4025294	G	A	9	GENIC	homozygous	63662061
20	4025634	4025635	C	T	18	GENIC	homozygous	63335522
20	4025824	4025825	C	T	8	GENIC	heterozygous	63662062
20	4025912	4025913	G	A	18	GENIC	homozygous	63662063
20	4026923	4026924	A	C	22	GENIC	homozygous	63563653
20	4027784	4027785	G	A	25	GENIC	homozygous	63662064
20	4027839	4027840	C	T	16	GENIC	homozygous	63563655
20	4027937	4027938	T	C	21	GENIC	homozygous	63335524
20	4028126	4028127	A	T	12	GENIC	homozygous	63335527
20	4028323	4028324	C	T	26	GENIC	possibly homozygous	63335528
20	4028715	4028716	T	C	25	GENIC	homozygous	63563657
20	4029781	4029782	G	A	14	GENIC	homozygous	63662065
20	4031099	4031100	C	A	10	GENIC	homozygous	63335530
20	4031401	4031402	A	G	28	GENIC	homozygous	63640932
20	4031404	4031405	G	A	28	GENIC	homozygous	63335532
20	4031613	4031614	G	A	14	GENIC	homozygous	63640933
20	4031705	4031706	C	A	18	GENIC	homozygous	63335534
20	4027375	4027376	G	A	24	GENIC	homozygous	63716626
20	4031666	4031667	C	T	20	GENIC	homozygous	63335533
20	4031752	4031753	A	T	20	GENIC	homozygous	63640934
20	4031831	4031832	C	T	22	GENIC	homozygous	63335535
20	4032037	4032038	G	A	16	GENIC	homozygous	63335537
20	4032261	4032262	C	T	24	GENIC	homozygous	63662067
20	4032872	4032873	G	A	19	GENIC	homozygous	63640935
20	4033226	4033227	G	A	8	GENIC	homozygous	63640936
20	4033604	4033605	G	T	12	GENIC	homozygous	63716627