chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	14604824	14604825	T	G	43	GENIC	heterozygous	119882202
20	14611163	14611164	T	C	53	GENIC	homozygous	109102903
20	14612584	14612585	A	G	34	GENIC	homozygous	109102905
20	14617121	14617122	A	G	39	GENIC	homozygous	109102922
20	14618066	14618067	T	C	67	GENIC	possibly homozygous	109102926
20	14620660	14620661	C	T	67	GENIC	possibly homozygous	109303570
20	14622004	14622005	C	G	34	GENIC	homozygous	109102936
20	14622424	14622425	G	A	34	GENIC	homozygous	109102940
20	14625835	14625836	G	A	55	GENIC	homozygous	109303574
20	14627421	14627422	G	A	23	GENIC	homozygous	109303576
20	14627542	14627543	C	T	26	GENIC	homozygous	109303578
20	14627774	14627775	G	A	50	GENIC	homozygous	109303580
20	14628382	14628383	C	T	66	GENIC	heterozygous	109493353
20	14628434	14628435	C	T	41	GENIC	heterozygous	109102957
20	14629271	14629272	C	T	72	GENIC	homozygous	109102967
20	14629537	14629538	A	T	39	GENIC	homozygous	109303582
20	14630469	14630470	G	A	37	GENIC	possibly homozygous	109102973
20	14630604	14630605	C	T	46	GENIC	homozygous	109303584
20	14632420	14632421	T	C	46	GENIC	possibly homozygous	109303586
20	14634543	14634544	C	G	44	GENIC	homozygous	109303588
20	14635772	14635773	C	T	36	GENIC	homozygous	109303590
20	14636602	14636603	A	G	23	GENIC	homozygous	109102993
20	14639215	14639216	T	C	35	GENIC	homozygous	109102997
20	14639494	14639495	C	T	36	GENIC	homozygous	109303592
20	14640632	14640633	C	T	56	GENIC	homozygous	109303594
20	14640930	14640931	C	T	37	GENIC	homozygous	109103005
20	14643592	14643593	A	G	21	GENIC	homozygous	109303596
20	14639929	14639930	T	C	84	GENIC	heterozygous	119871753
20	14639979	14639980	C	G	47	GENIC	heterozygous	119871754