chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	42302804	42302805	G	A	31	GENIC	possibly homozygous	111049944
17	42303336	42303337	C	T	25	GENIC	homozygous	111049946
17	42304080	42304081	T	C	23	GENIC	homozygous	111049948
17	42304091	42304092	G	A	24	GENIC	homozygous	111049950
17	42304149	42304150	T	C	19	GENIC	homozygous	111049952
17	42304276	42304277	T	A	13	GENIC	homozygous	111049954
17	42306572	42306573	G	A	17	GENIC	homozygous	111049962
17	42305183	42305184	C	T	35	GENIC	possibly homozygous	119285558
17	42305842	42305843	T	C	31	GENIC	homozygous	111049956
17	42306079	42306080	A	G	29	GENIC	homozygous	111049958
17	42306370	42306371	G	A	33	GENIC	homozygous	111049960
17	42307463	42307464	G	A	44	GENIC	homozygous	111049964
17	42308011	42308012	A	G	33	GENIC	homozygous	111049966
17	42308091	42308092	G	A	30	GENIC	homozygous	111049968
17	42308181	42308182	A	G	31	GENIC	homozygous	111049970
17	42308708	42308709	T	C	13	GENIC	homozygous	111049972
17	42309276	42309277	G	A	48	GENIC	homozygous	111049974
17	42310070	42310071	G	C	55	GENIC	homozygous	111049976