chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4022898	4022899	C	T	37	GENIC	homozygous	63563645
20	4023438	4023439	G	A	45	GENIC	homozygous	63563647
20	4025634	4025635	C	T	43	GENIC	homozygous	63335522
20	4025237	4025238	A	G	20	GENIC	homozygous	63335520
20	4026553	4026554	C	T	26	GENIC	homozygous	63563649
20	4026579	4026580	C	T	31	GENIC	possibly homozygous	63563651
20	4026923	4026924	A	C	36	GENIC	homozygous	63563653
20	4027839	4027840	C	T	37	GENIC	homozygous	63563655
20	4027937	4027938	T	C	21	GENIC	homozygous	63335524
20	4028126	4028127	A	T	29	GENIC	homozygous	63335527
20	4028323	4028324	C	T	15	GENIC	homozygous	63335528
20	4028715	4028716	T	C	30	GENIC	homozygous	63563657
20	4031099	4031100	C	A	40	GENIC	homozygous	63335530
20	4031193	4031194	G	T	40	GENIC	homozygous	63335531
20	4031404	4031405	G	A	41	GENIC	homozygous	63335532
20	4031666	4031667	C	T	25	GENIC	homozygous	63335533
20	4031705	4031706	C	A	23	GENIC	homozygous	63335534
20	4031831	4031832	C	T	43	GENIC	homozygous	63335535
20	4031940	4031941	A	T	38	GENIC	homozygous	63335536
20	4032037	4032038	G	A	35	GENIC	homozygous	63335537
20	4032542	4032543	G	A	37	GENIC	homozygous	63335538
20	4032675	4032676	C	T	23	GENIC	homozygous	63335539
20	4033164	4033165	G	C	11	GENIC	homozygous	63335541
20	4033618	4033619	A	G	20	GENIC	homozygous	63335542