chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90342513	90342514	T	G	39	GENIC	homozygous	116676110
10	90343212	90343213	G	C	44	GENIC	homozygous	116676112
10	90344897	90344898	G	T	37	GENIC	homozygous	116676114
10	90345386	90345387	T	G	42	GENIC	homozygous	116676116
10	90345484	90345485	A	G	34	GENIC	homozygous	116676118
10	90345840	90345841	G	A	42	GENIC	homozygous	116676120
10	90345928	90345929	G	A	50	GENIC	homozygous	116676122
10	90346312	90346313	T	C	40	GENIC	homozygous	116676124
10	90346569	90346570	C	T	32	GENIC	homozygous	116676126
10	90347054	90347055	C	T	26	GENIC	homozygous	116676128
10	90347545	90347546	G	T	32	GENIC	homozygous	117020548
10	90347574	90347575	A	G	18	GENIC	homozygous	116676130
10	90348037	90348038	T	C	36	GENIC	homozygous	116676132
10	90348248	90348249	A	G	38	GENIC	homozygous	116676134
10	90348274	90348275	A	G	42	GENIC	homozygous	116676136
10	90348285	90348286	T	C	41	GENIC	homozygous	116676138
10	90348684	90348685	T	C	48	GENIC	homozygous	116676140
10	90348890	90348891	C	G	28	GENIC	homozygous	116676142
10	90349357	90349358	C	A	30	GENIC	homozygous	116676144