chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	41047066	41047067	A	G	11	GENIC	homozygous	117331028
9	41047148	41047149	A	G	14	GENIC	homozygous	117716073
9	41047222	41047223	A	G	11	GENIC	homozygous	117716075
9	41047272	41047273	A	G	6	GENIC	homozygous	117716077
9	41047279	41047280	C	T	8	GENIC	homozygous	117716079
9	41047720	41047721	G	T	5	GENIC	homozygous	117716081
9	41047722	41047723	C	T	6	GENIC	homozygous	117716083
9	41047969	41047970	C	A	14	GENIC	homozygous	117331031
9	41048338	41048339	T	C	4	GENIC	homozygous	117331034
9	41048369	41048370	C	T	14	GENIC	homozygous	117331035
9	41048641	41048642	A	G	18	GENIC	homozygous	117331036
9	41050263	41050264	T	A	17	GENIC	homozygous	117331038
9	41050440	41050441	T	C	12	GENIC	homozygous	117864319
9	41050643	41050644	C	T	16	GENIC	homozygous	117864320
9	41051526	41051527	C	T	6	GENIC	homozygous	126514239
9	41051527	41051528	A	G	5	GENIC	heterozygous	126514241
9	41051547	41051548	A	G	3	GENIC	heterozygous	120405162
9	41051770	41051771	G	A	8	GENIC	homozygous	117864321
9	41051773	41051774	T	A	8	GENIC	homozygous	117864322
9	41051804	41051805	C	G	14	GENIC	homozygous	117331039
9	41051892	41051893	T	C	12	GENIC	homozygous	117864323