chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4021859	4021860	C	T	43	GENIC	homozygous	63335512
20	4022387	4022388	C	T	37	GENIC	possibly homozygous	63335513
20	4022581	4022582	C	T	49	GENIC	homozygous	63335514
20	4023154	4023155	A	G	33	GENIC	homozygous	63335515
20	4023283	4023284	T	C	30	GENIC	homozygous	63335516
20	4023429	4023430	G	A	49	GENIC	possibly homozygous	63335517
20	4023787	4023788	C	T	44	GENIC	homozygous	63335518
20	4023964	4023965	G	A	37	GENIC	homozygous	63335519
20	4025237	4025238	A	G	43	GENIC	homozygous	63335520
20	4025490	4025491	G	A	46	GENIC	possibly homozygous	63335521
20	4025634	4025635	C	T	60	GENIC	homozygous	63335522
20	4027598	4027599	G	A	31	GENIC	homozygous	63335523
20	4027937	4027938	T	C	29	GENIC	homozygous	63335524
20	4028036	4028037	G	A	53	GENIC	possibly homozygous	63335525
20	4028118	4028119	G	T	45	GENIC	homozygous	63335526
20	4028126	4028127	A	T	44	GENIC	homozygous	63335527
20	4028323	4028324	C	T	48	GENIC	homozygous	63335528
20	4029463	4029464	G	A	23	GENIC	homozygous	63335529
20	4031099	4031100	C	A	53	GENIC	homozygous	63335530
20	4031193	4031194	G	T	59	GENIC	homozygous	63335531
20	4031404	4031405	G	A	59	GENIC	homozygous	63335532
20	4031666	4031667	C	T	64	GENIC	homozygous	63335533
20	4031705	4031706	C	A	66	GENIC	possibly homozygous	63335534
20	4031831	4031832	C	T	43	GENIC	homozygous	63335535
20	4031940	4031941	A	T	46	GENIC	homozygous	63335536
20	4032037	4032038	G	A	48	GENIC	homozygous	63335537
20	4032542	4032543	G	A	43	GENIC	homozygous	63335538
20	4032675	4032676	C	T	52	GENIC	possibly homozygous	63335539
20	4033147	4033148	G	A	22	GENIC	heterozygous	63335540
20	4033164	4033165	G	C	19	GENIC	possibly homozygous	63335541
20	4033618	4033619	A	G	61	GENIC	homozygous	63335542