chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90342439	90342440	G	A	35	GENIC	homozygous	116951282
10	90342513	90342514	T	G	34	GENIC	homozygous	116676110
10	90342616	90342617	T	C	28	GENIC	homozygous	116951284
10	90343122	90343123	A	T	30	GENIC	homozygous	116951286
10	90343212	90343213	G	C	31	GENIC	homozygous	116676112
10	90343296	90343297	A	G	31	GENIC	homozygous	116904535
10	90343772	90343773	G	A	30	GENIC	homozygous	116904537
10	90343806	90343807	C	T	29	GENIC	homozygous	116951288
10	90344897	90344898	G	T	15	GENIC	homozygous	116676114
10	90345386	90345387	T	G	26	GENIC	homozygous	116676116
10	90345453	90345454	G	T	25	GENIC	homozygous	116951290
10	90345484	90345485	A	G	25	GENIC	homozygous	116676118
10	90345613	90345614	G	T	29	GENIC	homozygous	116904539
10	90345928	90345929	G	A	34	GENIC	homozygous	116676122
10	90345965	90345966	C	A	23	GENIC	homozygous	116951292
10	90346312	90346313	T	C	31	GENIC	homozygous	116676124
10	90348274	90348275	A	G	47	GENIC	homozygous	116676136
10	90348285	90348286	T	C	47	GENIC	homozygous	116676138
10	90348684	90348685	T	C	40	GENIC	homozygous	116676140
10	90349365	90349366	A	G	25	GENIC	homozygous	116904545
10	90349748	90349749	T	C	16	GENIC	homozygous	116904547
10	90350936	90350937	A	C	21	GENIC	homozygous	116904549
10	90348262	90348263	T	C	47	GENIC	homozygous	116982617
10	90348241	90348242	C	T	42	GENIC	homozygous	116982615