chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	24819227	24819228	C	T	12	GENIC	possibly homozygous	46031510
20	24819255	24819256	T	C	8	GENIC	homozygous	45490377
20	24820550	24820551	G	A	12	GENIC	possibly homozygous	46028363
20	24820636	24820637	T	C	20	GENIC	possibly homozygous	45490379
20	24820853	24820854	G	T	24	GENIC	homozygous	45490380
20	24821444	24821446	TT	--	2	GENIC	homozygous	45902022
20	24821481	24821482	A	G	8	GENIC	possibly homozygous	45490383
20	24821485	24821486	C	CT	4	GENIC	heterozygous	45490384
20	24821553	24821554	T	TTA	7	GENIC	homozygous	45490385
20	24822579	24822580	A	T	20	GENIC	homozygous	45490396
20	24822708	24822709	T	C	24	GENIC	possibly homozygous	45490397
20	24822994	24822995	A	G	20	GENIC	possibly homozygous	45490398
20	24823459	24823460	A	G	28	GENIC	homozygous	45982219
20	24823546	24823547	G	A	23	GENIC	possibly homozygous	45490400
20	24823627	24823628	C	A	33	GENIC	possibly homozygous	46028364
20	24824105	24824106	C	G	17	GENIC	homozygous	45490401
20	24824839	24824840	A	G	28	GENIC	homozygous	45490402
20	24828323	24828324	C	G	32	GENIC	possibly homozygous	46028365
20	24831230	24831231	A	ATC	25	GENIC	homozygous	45490415
20	24831450	24831451	C	CTTCTTTCT	3	GENIC	homozygous	45845537
20	24831500	24831501	T	G	6	GENIC	homozygous	46031511
20	24831504	24831505	T	G	6	GENIC	homozygous	46031512
20	24832146	24832147	A	-	17	GENIC	homozygous	46028366