chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3310059	3310060	G	A	3	GENIC	homozygous	109068410
20	3310981	3310982	A	G	11	GENIC	homozygous	109068414
20	3312721	3312722	A	C	19	GENIC	homozygous	109068418
20	3313233	3313234	C	T	13	GENIC	homozygous	109068420
20	3314181	3314182	T	C	21	GENIC	homozygous	109068422
20	3314521	3314522	T	C	22	GENIC	homozygous	109068424
20	3314872	3314873	C	T	33	GENIC	homozygous	109068426
20	3314963	3314964	G	A	26	GENIC	homozygous	109068428
20	3315125	3315126	G	A	31	GENIC	homozygous	109068430
20	3315166	3315167	C	T	25	GENIC	homozygous	109068432
20	3315315	3315316	T	C	6	GENIC	homozygous	109068434
20	3315320	3315321	T	A	6	GENIC	homozygous	109068436
20	3315352	3315353	C	A	11	GENIC	homozygous	109068438
20	3315394	3315395	C	A	19	GENIC	homozygous	109068440
20	3315396	3315397	A	G	20	GENIC	homozygous	109068442
20	3316212	3316213	C	A	13	GENIC	homozygous	109068446
20	3317096	3317097	G	C	28	GENIC	homozygous	109068450
20	3317158	3317159	G	C	22	GENIC	homozygous	109068452
20	3317206	3317207	C	T	10	GENIC	homozygous	109231532
20	3317207	3317208	G	T	10	GENIC	homozygous	109231533
20	3317211	3317212	C	T	17	GENIC	homozygous	109231534
20	3317980	3317981	T	C	22	GENIC	homozygous	109068456
20	3318802	3318803	A	G	17	GENIC	homozygous	109068458
20	3321287	3321288	G	A	19	GENIC	homozygous	109068460
20	3321375	3321376	C	T	22	GENIC	homozygous	109068462