chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	57623010	57623011	G	A	18	GENIC	homozygous	116785619
10	57624345	57624346	C	T	11	GENIC	homozygous	116785621
10	57625189	57625190	A	T	21	GENIC	homozygous	116604077
10	57625717	57625718	A	C	16	GENIC	homozygous	116604083
10	57627104	57627105	A	C	9	GENIC	homozygous	116785623
10	57627375	57627376	C	G	13	GENIC	homozygous	116785625
10	57627658	57627659	C	T	13	GENIC	homozygous	117011627
10	57628415	57628416	T	G	8	GENIC	homozygous	116604095
10	57629218	57629219	T	C	7	GENIC	homozygous	116604097
10	57629811	57629812	A	G	21	GENIC	homozygous	116604099
10	57629837	57629838	T	C	21	GENIC	homozygous	116604101
10	57630497	57630498	G	A	4	GENIC	homozygous	116785627
10	57630760	57630761	T	C	12	GENIC	homozygous	116604103
10	57630838	57630839	G	T	17	GENIC	homozygous	126383183
10	57630934	57630935	T	C	18	GENIC	homozygous	126383184
10	57631729	57631730	C	T	22	GENIC	homozygous	116785629
10	57632395	57632396	G	A	4	GENIC	heterozygous	116604107
10	57632568	57632569	A	T	16	GENIC	homozygous	116604111
10	57632632	57632633	C	A	11	GENIC	homozygous	116785633
10	57632975	57632976	T	C	15	GENIC	homozygous	116604115
10	57633085	57633086	C	T	16	GENIC	homozygous	116785635
10	57633511	57633512	C	T	13	GENIC	homozygous	116785637
10	57634311	57634312	G	A	16	GENIC	homozygous	116604119
10	57635350	57635351	C	T	14	GENIC	homozygous	116785639
10	57636025	57636026	C	T	9	GENIC	homozygous	116785641
10	57636248	57636249	G	C	23	GENIC	homozygous	116604123
10	57636336	57636337	A	C	9	GENIC	homozygous	126383186
10	57636912	57636913	T	G	8	GENIC	homozygous	116785643
10	57638040	57638041	T	C	6	GENIC	homozygous	116604125