chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	109727493	109727494	T	C	71	GENIC	homozygous	60789712
1	109727818	109727819	T	C	41	GENIC	homozygous	60789713
1	109728936	109728937	A	-	58	GENIC	homozygous	60789714
1	109729045	109729046	T	G	79	GENIC	homozygous	60789715
1	109729455	109729456	T	C	37	GENIC	homozygous	60789716
1	109730320	109730322	AT	--	21	GENIC	homozygous	60789717
1	109730351	109730352	C	CT	38	GENIC	homozygous	60789718
1	109730361	109730362	C	A	45	GENIC	homozygous	60789719
1	109730367	109730368	C	T	48	GENIC	homozygous	60789720
1	109730407	109730408	G	A	59	GENIC	homozygous	60789721
1	109730562	109730563	A	G	66	GENIC	homozygous	60789722
1	109730648	109730649	G	GA	59	GENIC	homozygous	60789723
1	109731042	109731043	A	G	51	GENIC	homozygous	60789724
1	109731470	109731471	A	T	63	GENIC	homozygous	60789725
1	109731617	109731618	T	C	64	GENIC	homozygous	60789726
1	109731920	109731921	T	A	54	GENIC	homozygous	60789727
1	109732178	109732179	A	G	78	GENIC	possibly homozygous	60789728
1	109732279	109732280	C	G	75	GENIC	homozygous	60789729
1	109732936	109732937	T	A	66	GENIC	homozygous	60789730
1	109733531	109733532	T	C	46	GENIC	homozygous	60789731
1	109733563	109733567	GTTT	----	42	GENIC	homozygous	60789732