chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3369139	3369140	G	A	28	GENIC	homozygous	109068607
20	3369349	3369350	C	A	30	GENIC	homozygous	109068609
20	3369454	3369455	C	T	36	GENIC	homozygous	109068611
20	3370226	3370227	T	C	26	GENIC	homozygous	109068613
20	3370361	3370362	C	T	30	GENIC	homozygous	109068615
20	3370380	3370381	T	A	26	GENIC	homozygous	109068617
20	3370695	3370696	T	C	24	GENIC	homozygous	109068619
20	3370991	3370992	C	A	24	GENIC	homozygous	109068621
20	3371868	3371869	A	G	19	GENIC	homozygous	109068627
20	3372479	3372480	C	A	16	GENIC	homozygous	109068629
20	3376855	3376856	C	T	28	GENIC	homozygous	109068633
20	3376997	3376998	G	C	25	GENIC	homozygous	109068635
20	3377322	3377323	C	T	21	GENIC	homozygous	109068639
20	3377324	3377325	A	G	21	GENIC	homozygous	109068641
20	3377443	3377444	A	G	26	GENIC	homozygous	109068643
20	3378598	3378599	T	C	40	GENIC	homozygous	109068645
20	3378649	3378650	G	C	27	GENIC	homozygous	109068647
20	3379237	3379238	T	C	38	GENIC	homozygous	109068653
20	3379399	3379400	G	A	30	GENIC	homozygous	109068655
20	3379818	3379819	A	G	24	GENIC	homozygous	109068657
20	3380531	3380532	T	C	40	GENIC	homozygous	109294418
20	3381033	3381034	C	T	24	GENIC	homozygous	109068661
20	3381157	3381158	C	A	20	GENIC	homozygous	109068663
20	3381536	3381537	A	G	29	GENIC	homozygous	109068667
20	3382561	3382562	C	T	20	GENIC	homozygous	109068669
20	3382661	3382662	G	A	21	GENIC	homozygous	109068671
20	3384425	3384426	C	T	29	GENIC	homozygous	109068673
20	3384758	3384759	A	G	25	GENIC	homozygous	109068675
20	3385878	3385879	G	A	11	GENIC	homozygous	109068677
20	3385935	3385936	T	C	8	GENIC	homozygous	109231546
20	3385970	3385971	T	C	10	GENIC	homozygous	109068679
20	3372219	3372220	G	C	3	GENIC	homozygous	109417134
20	3384770	3384771	G	A	23	GENIC	homozygous	109417136