chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	104388264	104388265	G	A	21	GENIC	homozygous	117611935
9	104389152	104389153	A	G	20	GENIC	homozygous	117631581
9	104389561	104389562	A	C	19	GENIC	homozygous	117611937
9	104389923	104389924	A	G	26	GENIC	homozygous	117631585
9	104390176	104390177	G	A	19	GENIC	homozygous	117631587
9	104391038	104391039	T	C	21	GENIC	homozygous	117631589
9	104392741	104392742	A	G	21	GENIC	homozygous	117611939
9	104394003	104394004	G	A	24	GENIC	homozygous	117611941
9	104394458	104394459	C	T	18	GENIC	homozygous	117631593
9	104396457	104396458	C	T	18	GENIC	homozygous	117611943
9	104397245	104397246	C	T	24	GENIC	homozygous	117611945
9	104397486	104397487	A	T	18	GENIC	homozygous	117611947
9	104397773	104397774	C	T	16	GENIC	homozygous	117611950
9	104398110	104398111	T	C	11	GENIC	homozygous	117611952
9	104398833	104398834	A	G	17	GENIC	homozygous	117611954
9	104398869	104398870	C	T	17	GENIC	homozygous	117611956
9	104403188	104403189	G	T	22	GENIC	homozygous	117631597
9	104404725	104404726	C	G	15	GENIC	homozygous	117611958
9	104407349	104407350	C	T	19	GENIC	homozygous	117631601
9	104410517	104410518	A	G	16	GENIC	homozygous	117631607
9	104411112	104411113	A	G	18	GENIC	homozygous	117611968
9	104411144	104411145	G	C	11	GENIC	homozygous	117611970
9	104411468	104411469	C	T	20	GENIC	homozygous	117631609
9	104412740	104412741	C	T	28	GENIC	homozygous	117611972
9	104413101	104413102	G	A	14	GENIC	homozygous	117611974
9	104413213	104413214	T	C	19	GENIC	homozygous	117631613
9	104415976	104415977	T	G	21	GENIC	homozygous	117631629
9	104416166	104416167	C	T	18	GENIC	homozygous	117611984
9	104417212	104417213	A	C	27	GENIC	homozygous	117611986
9	104418304	104418305	A	C	26	GENIC	homozygous	117631631
9	104418403	104418404	C	T	13	GENIC	homozygous	117631633