chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	80154571	80154572	A	G	50	GENIC	homozygous	120270028
9	80154643	80154644	G	A	53	GENIC	homozygous	120270029
9	80154696	80154697	A	C	61	GENIC	homozygous	120270030
9	80154969	80154970	T	C	57	GENIC	homozygous	120270031
9	80154991	80154992	G	T	51	GENIC	homozygous	120270032
9	80155177	80155178	C	T	69	GENIC	homozygous	120270033
9	80155531	80155532	G	A	52	GENIC	homozygous	120270034
9	80155664	80155665	A	G	70	GENIC	homozygous	120270035
9	80155983	80155984	G	A	53	GENIC	homozygous	120270036
9	80156022	80156023	A	G	51	GENIC	homozygous	120270037
9	80156201	80156202	A	T	73	GENIC	homozygous	120270038
9	80156310	80156311	T	C	61	GENIC	homozygous	120270039
9	80156398	80156399	C	A	60	GENIC	possibly homozygous	120270040
9	80156452	80156453	G	A	61	GENIC	homozygous	120270041
9	80156865	80156866	A		46	GENIC	homozygous	128727205
9	80157526	80157527	A	G	63	GENIC	homozygous	120270042
9	80157666	80157667	A	G	60	GENIC	homozygous	120270043
9	80160151	80160152	G	A	55	GENIC	homozygous	117848246
9	80160426	80160427	T	G	58	GENIC	homozygous	117848247
9	80163030	80163031	G	A	48	GENIC	homozygous	117848248
9	80163811	80163812	A	T	45	GENIC	homozygous	117879393
9	80162519	80162520	A		49	GENIC	possibly homozygous	128727206
9	80157748	80157748		C	73	GENIC	homozygous	131071635
9	80163402	80163403	T	C	50	GENIC	homozygous	117879389
9	80166545	80166546	G	C	41	GENIC	homozygous	117848251
9	80166548	80166549	G	T	40	GENIC	homozygous	117879399
9	80161551	80161552	A		54	GENIC	homozygous	131071636