chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3310938	3310939	T	G	28	GENIC	homozygous	109370704
20	3310981	3310982	A	G	34	GENIC	homozygous	109068414
20	3311423	3311424	A	T	49	GENIC	homozygous	109370706
20	3312129	3312130	C	T	23	GENIC	homozygous	109370709
20	3312681	3312682	G	A	42	GENIC	homozygous	109370711
20	3314643	3314644	T	A	47	GENIC	homozygous	109370713
20	3314666	3314667	T	C	42	GENIC	homozygous	109490464
20	3314717	3314718	T	C	43	GENIC	homozygous	109490466
20	3315125	3315126	G	A	26	GENIC	homozygous	109068430
20	3315165	3315166	G	A	33	GENIC	homozygous	109490468
20	3315681	3315682	G	A	26	GENIC	homozygous	109370715
20	3315725	3315726	A	C	19	GENIC	homozygous	109370717
20	3315891	3315892	G	A	19	GENIC	homozygous	109370719
20	3316212	3316213	C	A	32	GENIC	homozygous	109068446
20	3317096	3317097	G	C	24	GENIC	homozygous	109068450
20	3317287	3317288	C	T	44	GENIC	homozygous	109370721
20	3317295	3317296	G	A	47	GENIC	homozygous	109370723
20	3317694	3317695	T	C	26	GENIC	homozygous	109068454
20	3317980	3317981	T	C	30	GENIC	homozygous	109068456
20	3319117	3319118	C	T	28	GENIC	homozygous	109370725