chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3310981	3310982	A	G	19	GENIC	homozygous	109068414
20	3311096	3311097	T	A	10	GENIC	homozygous	109417032
20	3314181	3314182	T	C	21	GENIC	homozygous	109068422
20	3314234	3314235	C	T	21	GENIC	homozygous	109417034
20	3314537	3314538	G	A	15	GENIC	homozygous	109417037
20	3314699	3314700	A	T	4	GENIC	homozygous	109417039
20	3314872	3314873	C	T	11	GENIC	homozygous	109068426
20	3314963	3314964	G	A	26	GENIC	homozygous	109068428
20	3315125	3315126	G	A	23	GENIC	homozygous	109068430
20	3315166	3315167	C	T	24	GENIC	homozygous	109068432
20	3315315	3315316	T	C	23	GENIC	homozygous	109068434
20	3315320	3315321	T	A	25	GENIC	homozygous	109068436
20	3315352	3315353	C	A	23	GENIC	homozygous	109068438
20	3315394	3315395	C	A	30	GENIC	homozygous	109068440
20	3315396	3315397	A	G	30	GENIC	homozygous	109068442
20	3316084	3316085	C	G	35	GENIC	homozygous	109417041
20	3316337	3316338	G	C	31	GENIC	homozygous	109417043
20	3317970	3317971	C	A	24	GENIC	homozygous	109417045
20	3318714	3318715	T	C	45	GENIC	homozygous	109417047
20	3317343	3317344	C	T	40	GENIC	homozygous	109388924