chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	106845394	106845395	A	T	57	GENIC	homozygous	138409184
8	106846351	106846352	T	C	70	GENIC	homozygous	138409185
8	106847097	106847098	C	T	46	GENIC	homozygous	138409186
8	106847660	106847661	G	A	41	GENIC	homozygous	138409187
8	106847680	106847681	C	T	45	GENIC	homozygous	138409188
8	106848010	106848011	T	C	53	GENIC	possibly homozygous	138409189
8	106848712	106848713	G	A	42	GENIC	homozygous	138409190
8	106849267	106849268	C	T	58	GENIC	homozygous	138409191
8	106850372	106850373	A	G	28	GENIC	homozygous	138409192
8	106850659	106850660	T	G	25	GENIC	homozygous	138409193
8	106853600	106853601	T	A	47	GENIC	homozygous	138409194
8	106854335	106854336	C	T	77	GENIC	homozygous	138409195
8	106856848	106856849	A	T	54	GENIC	homozygous	138409196
8	106853248	106853248		GATGATGACGATGACGACGAC	60	GENIC	homozygous	138263080
8	106853238	106853238		TAA	61	GENIC	homozygous	138263079