chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3329727	3329728	A	C	25	GENIC	homozygous	109068492
20	3329728	3329729	C	A	25	GENIC	homozygous	109068494
20	3329904	3329905	G	A	11	GENIC	homozygous	109068496
20	3330179	3330180	C	A	20	GENIC	homozygous	109068502
20	3330981	3330982	T	C	11	GENIC	homozygous	109068504
20	3331502	3331503	G	C	12	GENIC	homozygous	109294414
20	3331545	3331546	A	C	16	GENIC	homozygous	109068506
20	3331546	3331547	G	A	16	GENIC	homozygous	109068508
20	3331552	3331553	A	C	17	GENIC	homozygous	109068510
20	3331586	3331587	C	G	19	GENIC	homozygous	109068513
20	3331922	3331923	T	C	28	GENIC	homozygous	109068515
20	3334064	3334065	G	A	25	GENIC	homozygous	109068517
20	3334878	3334879	T	C	20	GENIC	homozygous	109068519
20	3335256	3335257	C	T	16	GENIC	homozygous	109068521
20	3335300	3335301	A	G	19	GENIC	homozygous	109068523
20	3335307	3335308	T	G	19	GENIC	homozygous	109068525
20	3336571	3336572	G	A	18	GENIC	homozygous	109068527
20	3337487	3337488	G	A	30	GENIC	homozygous	109068529
20	3339852	3339853	A	G	27	GENIC	homozygous	109068531
20	3340095	3340096	A	G	30	GENIC	homozygous	109068533
20	3340656	3340657	C	T	28	GENIC	homozygous	109068535
20	3341615	3341616	G	A	39	GENIC	homozygous	109068537
20	3342130	3342131	G	A	15	GENIC	homozygous	109068539
20	3342530	3342531	A	C	11	GENIC	homozygous	109068541
20	3342752	3342753	T	A	26	GENIC	homozygous	109068547
20	3342753	3342754	C	T	25	GENIC	homozygous	109068549
20	3344182	3344183	C	T	10	GENIC	homozygous	109068551