chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90342439	90342440	G	A	9	GENIC	homozygous	116951282
10	90342513	90342514	T	G	14	GENIC	homozygous	116676110
10	90343212	90343213	G	C	20	GENIC	homozygous	116676112
10	90343296	90343297	A	G	17	GENIC	homozygous	116904535
10	90343772	90343773	G	A	28	GENIC	homozygous	116904537
10	90344897	90344898	G	T	30	GENIC	homozygous	116676114
10	90345386	90345387	T	G	19	GENIC	homozygous	116676116
10	90345484	90345485	A	G	16	GENIC	homozygous	116676118
10	90345613	90345614	G	T	19	GENIC	homozygous	116904539
10	90345928	90345929	G	A	12	GENIC	homozygous	116676122
10	90346025	90346026	A	C	11	GENIC	heterozygous	117392104
10	90346312	90346313	T	C	11	GENIC	homozygous	116676124
10	90347331	90347332	T	G	25	GENIC	homozygous	117020547
10	90347574	90347575	A	G	20	GENIC	homozygous	116676130
10	90348029	90348030	C	T	18	GENIC	homozygous	116904541
10	90348248	90348249	A	G	10	GENIC	homozygous	116676134
10	90348274	90348275	A	G	9	GENIC	homozygous	116676136
10	90348675	90348676	A	T	21	GENIC	homozygous	116904543
10	90348684	90348685	T	C	21	GENIC	homozygous	116676140
10	90349365	90349366	A	G	16	GENIC	homozygous	116904545
10	90349748	90349749	T	C	17	GENIC	homozygous	116904547
10	90350936	90350937	A	C	20	GENIC	homozygous	116904549