chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	42302804	42302805	G	A	11	GENIC	homozygous	111049944
17	42303336	42303337	C	T	30	GENIC	homozygous	111049946
17	42303673	42303674	G	T	18	GENIC	homozygous	111465352
17	42304080	42304081	T	C	10	GENIC	homozygous	111049948
17	42304091	42304092	G	A	11	GENIC	homozygous	111049950
17	42304149	42304150	T	C	26	GENIC	homozygous	111049952
17	42304276	42304277	T	A	23	GENIC	homozygous	111049954
17	42305842	42305843	T	C	13	GENIC	homozygous	111049956
17	42306079	42306080	A	G	33	GENIC	homozygous	111049958
17	42306370	42306371	G	A	25	GENIC	homozygous	111049960
17	42306572	42306573	G	A	37	GENIC	homozygous	111049962
17	42307463	42307464	G	A	27	GENIC	homozygous	111049964
17	42308011	42308012	A	G	38	GENIC	homozygous	111049966
17	42308091	42308092	G	A	36	GENIC	homozygous	111049968
17	42308181	42308182	A	G	33	GENIC	homozygous	111049970
17	42309276	42309277	G	A	20	GENIC	homozygous	111049974
17	42310070	42310071	G	C	26	GENIC	homozygous	111049976