chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3310353	3310354	A	T	9	GENIC	homozygous	125215360
20	3312129	3312130	C	T	17	GENIC	homozygous	109370709
20	3312681	3312682	G	A	14	GENIC	homozygous	109370711
20	3314181	3314182	T	C	28	GENIC	homozygous	109068422
20	3314234	3314235	C	T	10	GENIC	homozygous	109417034
20	3314872	3314873	C	T	18	GENIC	homozygous	109068426
20	3314963	3314964	G	A	20	GENIC	homozygous	109068428
20	3315166	3315167	C	T	9	GENIC	homozygous	109068432
20	3315396	3315397	A	G	6	GENIC	homozygous	109068442
20	3315681	3315682	G	A	14	GENIC	homozygous	109370715
20	3316044	3316045	G	A	10	GENIC	homozygous	109454642
20	3316212	3316213	C	A	10	GENIC	homozygous	109068446
20	3316689	3316690	T	A	17	GENIC	homozygous	109068448
20	3316775	3316776	G	A	19	GENIC	homozygous	119856788
20	3317096	3317097	G	C	11	GENIC	homozygous	109068450
20	3317158	3317159	G	C	22	GENIC	homozygous	109068452
20	3317206	3317207	C	T	4	GENIC	homozygous	109231532
20	3317207	3317208	G	T	4	GENIC	homozygous	109231533
20	3317211	3317212	C	T	4	GENIC	homozygous	109231534
20	3317343	3317344	C	T	22	GENIC	homozygous	109388924
20	3317694	3317695	T	C	24	GENIC	homozygous	109068454
20	3317980	3317981	T	C	11	GENIC	homozygous	109068456
20	3318802	3318803	A	G	23	GENIC	homozygous	109068458
20	3320325	3320326	C	T	13	GENIC	homozygous	109388925
20	3321287	3321288	G	A	17	GENIC	homozygous	109068460
20	3321375	3321376	C	T	21	GENIC	homozygous	109068462
20	3321763	3321764	G	T	20	GENIC	homozygous	109388926
20	3322053	3322054	A	T	10	GENIC	homozygous	109068464
20	3315088	3315089	C	A	4	GENIC	heterozygous	125231422
20	3316900	3316901	A	T	6	GENIC	heterozygous	125231423
20	3316737	3316738	G	A	5	GENIC	homozygous	119756122