chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	9912012	9912013	T	C	3	GENIC	homozygous	51616110
10	9912020	9912021	T	C	7	GENIC	homozygous	51616111
10	9913261	9913262	A	T	26	GENIC	heterozygous	52027449
10	9912255	9912256	C	CGG	2	GENIC	homozygous	52027441
10	9912459	9912460	A	G	24	GENIC	homozygous	52027443
10	9913124	9913125	T	G	17	GENIC	possibly homozygous	52027445
10	9913165	9913166	G	A	27	GENIC	homozygous	52027447
10	9913344	9913345	A	G	27	GENIC	homozygous	51616114
10	9913697	9913698	G	T	10	GENIC	homozygous	51616115
10	9913699	9913700	G	A	11	GENIC	possibly homozygous	52027451
10	9913824	9913825	A	C	21	GENIC	homozygous	51616116
10	9913960	9913961	G	-	6	GENIC	homozygous	52027453
10	9914118	9914119	C	T	21	GENIC	possibly homozygous	52027455
10	9914140	9914141	G	-	16	GENIC	possibly homozygous	52027457
10	9914191	9914192	A	G	28	GENIC	possibly homozygous	51616117
10	9914220	9914221	G	T	33	GENIC	homozygous	52027459
10	9914475	9914476	A	G	22	GENIC	homozygous	51616118
10	9915254	9915255	T	TC	16	GENIC	heterozygous	51616121
10	9916302	9916303	A	-	4	GENIC	homozygous	52027461
10	9916450	9916451	T	A	6	GENIC	heterozygous	51616124
10	9917759	9917760	A	G	16	GENIC	possibly homozygous	51616126
10	9918323	9918324	A	G	21	GENIC	heterozygous	51323669
10	9913667	9913668	C	A	28	GENIC	possibly homozygous	51323666
10	9916592	9916593	T	TC	18	GENIC	possibly homozygous	51323667
10	9918840	9918841	C	T	17	GENIC	homozygous	52027465
10	9918849	9918850	T	C	19	GENIC	homozygous	52027467
10	9918996	9918997	T	C	14	GENIC	possibly homozygous	52027469
10	9919164	9919165	T	C	21	GENIC	possibly homozygous	52027471