chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5071390	5071391	G	T	43	GENIC	homozygous	109076435
20	5071494	5071495	T	A	30	GENIC	homozygous	109076437
20	5071659	5071660	C	T	22	GENIC	possibly homozygous	109076439
20	5071946	5071947	T	C	20	GENIC	homozygous	109076441
20	5072184	5072185	G	T	42	GENIC	homozygous	109233788
20	5072255	5072256	A	G	47	GENIC	homozygous	109329661
20	5072891	5072892	A	T	24	GENIC	possibly homozygous	109076443
20	5072994	5072995	G	A	18	GENIC	homozygous	109076445
20	5072998	5072999	A	T	18	GENIC	homozygous	109076447
20	5073003	5073004	C	T	19	GENIC	homozygous	109076449
20	5073010	5073011	C	T	21	GENIC	homozygous	109076451
20	5073012	5073013	A	C	21	GENIC	homozygous	109076453
20	5073514	5073515	T	C	28	GENIC	homozygous	109076457
20	5073866	5073867	G	A	33	GENIC	homozygous	109076459
20	5074367	5074368	G	T	12	GENIC	homozygous	109076461
20	5074389	5074390	C	G	8	GENIC	homozygous	109233791
20	5074512	5074513	G	A	18	GENIC	homozygous	109076467
20	5074606	5074607	A	G	17	GENIC	homozygous	109076469
20	5075058	5075059	G	T	32	GENIC	homozygous	109076471
20	5075065	5075066	G	A	33	GENIC	homozygous	109076473
20	5075451	5075452	G	A	26	GENIC	homozygous	109233792
20	5075610	5075611	A	G	25	GENIC	homozygous	109233793
20	5075683	5075684	A	G	25	GENIC	homozygous	109076475
20	5075898	5075899	G	A	37	GENIC	homozygous	109076477
20	5075908	5075909	G	A	41	GENIC	homozygous	109076479
20	5076282	5076283	A	G	15	GENIC	homozygous	109076481
20	5076354	5076355	A	G	23	GENIC	homozygous	109076483
20	5076389	5076390	T	C	27	GENIC	homozygous	109076485
20	5076509	5076510	A	G	16	GENIC	homozygous	109076489
20	5076543	5076544	G	A	17	GENIC	homozygous	109329663