chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	55013851	55013852	G	A	21	GENIC	homozygous	116602024
10	55014844	55014845	A	G	41	GENIC	homozygous	117130658
10	55014914	55014915	C	A	36	GENIC	homozygous	116602033
10	55016633	55016634	A	G	16	GENIC	homozygous	116602047
10	55016669	55016670	G	T	21	GENIC	homozygous	116602051
10	55019305	55019306	A	G	31	GENIC	homozygous	117130659
10	55020872	55020873	A	G	21	GENIC	homozygous	116602057
10	55022218	55022219	C	T	19	GENIC	homozygous	117130660
10	55022271	55022272	C	T	20	GENIC	homozygous	117130661
10	55022732	55022733	A	G	15	GENIC	homozygous	117151073
10	55023600	55023601	A	G	37	GENIC	homozygous	117011397
10	55024151	55024152	G	A	11	GENIC	homozygous	117130662
10	55025414	55025415	A	T	32	GENIC	homozygous	116781613
10	55025416	55025417	G	T	33	GENIC	homozygous	116781615
10	55025553	55025554	G	T	34	GENIC	homozygous	116602061
10	55025811	55025812	T	A	29	GENIC	homozygous	116602063
10	55026503	55026504	T	G	51	GENIC	homozygous	117151074
10	55029354	55029355	C	A	38	GENIC	homozygous	117130663
10	55030286	55030287	C	G	23	GENIC	homozygous	116602075
10	55030665	55030666	A	G	37	GENIC	homozygous	116602077
10	55031923	55031924	G	T	28	GENIC	homozygous	116602079