chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	48569691	48569692	G	A	61	GENIC	homozygous	117391283
10	48570381	48570382	G	A	59	GENIC	homozygous	117253389
10	48570410	48570411	G	A	69	GENIC	homozygous	117253391
10	48570803	48570804	C	T	32	GENIC	homozygous	133681341
10	48571586	48571587	A	G	67	GENIC	homozygous	116879966
10	48570885	48570886	G	C	20	GENIC	heterozygous	133236722
10	48570887	48570888	T	C	21	GENIC	heterozygous	133236723
10	48572789	48572790	T	A	32	GENIC	homozygous	133681342
10	48573661	48573662	C	T	56	GENIC	homozygous	116879968
10	48574155	48574156	T	C	53	GENIC	homozygous	116879970
10	48574811	48574812	G	A	58	GENIC	possibly homozygous	117253393
10	48575201	48575202	G	A	47	GENIC	homozygous	117253395
10	48575237	48575238	C	G	58	GENIC	homozygous	116879972
10	48577034	48577035	A	G	51	GENIC	homozygous	116879978
10	48580398	48580399	C	G	51	GENIC	homozygous	116879980
10	48584599	48584599		GTTTT	33	GENIC	homozygous	131092886
10	48580540	48580540		T	59	GENIC	homozygous	128815258
10	48572804	48572810	ATACAT		35	GENIC	possibly homozygous	133680302
10	48580112	48580112		AAC	48	GENIC	homozygous	133680303