chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5071248	5071249	C	T	45	GENIC	homozygous	109076433
20	5071390	5071391	G	T	31	GENIC	homozygous	109076435
20	5071494	5071495	T	A	14	GENIC	homozygous	109076437
20	5071659	5071660	C	T	38	GENIC	homozygous	109076439
20	5071888	5071889	C	A	38	GENIC	homozygous	109296757
20	5071946	5071947	T	C	47	GENIC	homozygous	109076441
20	5072184	5072185	G	T	57	GENIC	homozygous	109233788
20	5072854	5072855	G	C	21	GENIC	homozygous	109296759
20	5072891	5072892	A	T	22	GENIC	homozygous	109076443
20	5072994	5072995	G	A	27	GENIC	homozygous	109076445
20	5072998	5072999	A	T	30	GENIC	homozygous	109076447
20	5073003	5073004	C	T	29	GENIC	homozygous	109076449
20	5073010	5073011	C	T	30	GENIC	homozygous	109076451
20	5073012	5073013	A	C	31	GENIC	homozygous	109076453
20	5073269	5073270	C	A	20	GENIC	homozygous	109296761
20	5073442	5073443	T	C	29	GENIC	homozygous	109076455
20	5073514	5073515	T	C	47	GENIC	homozygous	109076457
20	5073851	5073852	C	T	21	GENIC	homozygous	109296763
20	5073866	5073867	G	A	23	GENIC	homozygous	109076459
20	5074083	5074084	G	C	32	GENIC	homozygous	109296765
20	5074391	5074392	G	C	28	GENIC	homozygous	109076463
20	5074462	5074463	A	C	44	GENIC	homozygous	109076465
20	5074467	5074468	T	A	46	GENIC	homozygous	109296767
20	5074512	5074513	G	A	41	GENIC	homozygous	109076467
20	5074606	5074607	A	G	43	GENIC	homozygous	109076469
20	5074913	5074914	C	T	34	GENIC	homozygous	109296769
20	5075058	5075059	G	T	19	GENIC	homozygous	109076471
20	5075065	5075066	G	A	20	GENIC	homozygous	109076473
20	5075683	5075684	A	G	42	GENIC	homozygous	109076475
20	5075898	5075899	G	A	35	GENIC	homozygous	109076477
20	5075908	5075909	G	A	33	GENIC	homozygous	109076479
20	5076282	5076283	A	G	6	GENIC	homozygous	109076481
20	5076354	5076355	A	G	14	GENIC	homozygous	109076483
20	5076389	5076390	T	C	17	GENIC	homozygous	109076485
20	5076439	5076440	C	T	21	GENIC	homozygous	109076487
20	5076509	5076510	A	G	27	GENIC	homozygous	109076489
20	5076622	5076623	C	T	29	GENIC	homozygous	109296771