chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	105690736	105690737	A	T	52	GENIC	homozygous	138648368
9	105691229	105691229		A	48	GENIC	homozygous	138478346
9	105691908	105691909	C		69	GENIC	homozygous	138478347
9	105692395	105692396	G	A	62	GENIC	homozygous	138648369
9	105695751	105695752	G	C	65	GENIC	homozygous	138648370
9	105696481	105696482	G	A	47	GENIC	homozygous	138648371
9	105699144	105699144		A	38	GENIC	homozygous	138478348
9	105701266	105701268	AA		46	GENIC	homozygous	138478349
9	105701435	105701436	T	C	46	GENIC	homozygous	138648372
9	105702408	105702409	A	C	47	GENIC	possibly homozygous	138648373
9	105703128	105703129	G	A	48	GENIC	homozygous	138648374
9	105706561	105706561		AT	37	GENIC	homozygous	138478351
9	105707204	105707204		CC	57	GENIC	homozygous	138478352
9	105708540	105708541	T	C	62	GENIC	homozygous	138648375
9	105709182	105709183	T	C	56	GENIC	homozygous	138648376
9	105710294	105710295	T	C	59	GENIC	homozygous	138648377