chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	57623010	57623011	G	A	55	GENIC	homozygous	116785619
10	57624345	57624346	C	T	51	GENIC	homozygous	116785621
10	57625189	57625190	A	T	65	GENIC	homozygous	116604077
10	57625717	57625718	A	C	35	GENIC	homozygous	116604083
10	57627104	57627105	A	C	49	GENIC	homozygous	116785623
10	57627375	57627376	C	G	33	GENIC	homozygous	116785625
10	57627658	57627659	C	T	36	GENIC	homozygous	117011627
10	57628415	57628416	T	G	33	GENIC	homozygous	116604095
10	57629218	57629219	T	C	32	GENIC	homozygous	116604097
10	57629811	57629812	A	G	50	GENIC	homozygous	116604099
10	57629837	57629838	T	C	46	GENIC	homozygous	116604101
10	57630497	57630498	G	A	32	GENIC	homozygous	116785627
10	57630760	57630761	T	C	46	GENIC	homozygous	116604103
10	57631729	57631730	C	T	39	GENIC	homozygous	116785629
10	57632568	57632569	A	T	36	GENIC	homozygous	116604111
10	57632632	57632633	C	A	39	GENIC	homozygous	116785633
10	57632975	57632976	T	C	53	GENIC	possibly homozygous	116604115
10	57633085	57633086	C	T	50	GENIC	homozygous	116785635
10	57633511	57633512	C	T	58	GENIC	homozygous	116785637
10	57634311	57634312	G	A	34	GENIC	homozygous	116604119
10	57635350	57635351	C	T	38	GENIC	homozygous	116785639
10	57636025	57636026	C	T	59	GENIC	homozygous	116785641
10	57636248	57636249	G	C	42	GENIC	homozygous	116604123
10	57636912	57636913	T	G	25	GENIC	homozygous	116785643
10	57638040	57638041	T	C	40	GENIC	homozygous	116604125