chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4593546	4593547	G	A	6	GENIC	homozygous	109329596
20	4598426	4598427	C	A	26	GENIC	possibly homozygous	109074825
20	4598428	4598429	C	A	31	GENIC	homozygous	109074827
20	4598729	4598730	G	A	24	GENIC	homozygous	109329598
20	4598775	4598776	C	A	42	GENIC	homozygous	109329600
20	4598948	4598949	C	T	27	GENIC	homozygous	109074829
20	4599033	4599034	G	A	19	GENIC	homozygous	109329603
20	4599344	4599345	G	A	21	GENIC	homozygous	109074835
20	4601137	4601138	G	A	11	GENIC	homozygous	109329605
20	4603411	4603412	T	G	17	GENIC	homozygous	109233547
20	4603508	4603509	C	A	20	GENIC	homozygous	109074843
20	4604312	4604313	G	A	16	GENIC	homozygous	109074849
20	4604395	4604396	T	C	29	GENIC	homozygous	109296184
20	4604400	4604401	A	G	29	GENIC	homozygous	109296186
20	4605201	4605202	A	C	18	GENIC	homozygous	109074851
20	4605408	4605409	T	A	30	GENIC	homozygous	109329607
20	4605480	4605481	A	T	34	GENIC	homozygous	109074853
20	4605773	4605774	G	A	29	GENIC	homozygous	109074855
20	4606252	4606253	A	G	35	GENIC	homozygous	109074858
20	4606879	4606880	C	A	25	GENIC	homozygous	109074860
20	4607252	4607253	T	G	23	GENIC	homozygous	109074862
20	4607420	4607421	C	T	20	GENIC	homozygous	109074864
20	4607834	4607835	T	G	22	GENIC	homozygous	109074868
20	4608156	4608157	T	C	11	GENIC	homozygous	109074872
20	4608594	4608595	A	C	12	GENIC	homozygous	109074876
20	4608606	4608607	G	T	13	GENIC	homozygous	109074878
20	4608635	4608636	T	C	15	GENIC	homozygous	109074880
20	4608756	4608757	G	A	36	GENIC	homozygous	109074882