chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	49233006	49233007	T	C	43	GENIC	homozygous	117253744
10	49234949	49234956	CCGGTTT		22	GENIC	homozygous	131093185
10	49238713	49238714	C	T	37	GENIC	homozygous	117253746
10	49238927	49238927		CCAAGGAAGACGGATTGTTTGCTTTGCAGTTTAGGAAGGATCTTGGT	39	GENIC	homozygous	131093191
10	49240489	49240489		CTCTCTGT	13	GENIC	homozygous	131093192
10	49241190	49241191	G	A	35	GENIC	homozygous	116882111
10	49242022	49242023	C	A	34	GENIC	homozygous	116882115
10	49239487	49239488	T	A	23	GENIC	homozygous	118083210
10	49242829	49242831	AG		30	GENIC	homozygous	132145339
10	49243120	49243121	A	G	37	GENIC	homozygous	117129709
10	49244947	49244948	C	T	27	GENIC	homozygous	117253748
10	49245106	49245107	C	T	33	GENIC	homozygous	117253750
10	49246576	49246577	T	C	50	GENIC	homozygous	117253752
10	49246931	49246934	CCC		36	GENIC	homozygous	131093197
10	49247131	49247132	A	G	47	GENIC	homozygous	116882183
10	49247672	49247673	A	G	44	GENIC	homozygous	116882191
10	49248280	49248281	T	C	55	GENIC	homozygous	116882201
10	49248727	49248728	T	C	48	GENIC	homozygous	116882207
10	49249584	49249585	T	C	59	GENIC	homozygous	116882213
10	49250210	49250211	A	T	56	GENIC	homozygous	117253754
10	49250795	49250796	C	T	39	GENIC	homozygous	117253756
10	49250919	49250920	A	G	46	GENIC	homozygous	116882220
10	49251178	49251182	TTTT		31	GENIC	homozygous	133680379
10	49252442	49252443	A	G	42	GENIC	homozygous	116882222
10	49252939	49252940	A	G	8	GENIC	homozygous	116882224
10	49253686	49253687	C	A	42	GENIC	homozygous	117253758
10	49254312	49254313	G	A	40	GENIC	homozygous	117253760
10	49254646	49254647	T	A	55	GENIC	homozygous	117253762