chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	97279239	97279240	A		12	GENIC	homozygous	128618683
8	97279250	97279251	G		13	GENIC	homozygous	128618684
8	97279263	97279264	T		13	GENIC	homozygous	128618685
8	97279267	97279268	G	C	13	GENIC	homozygous	128664487
8	97279269	97279272	CGT		13	GENIC	homozygous	128618686
8	97279273	97279278	TACGC		13	GENIC	homozygous	128618687
8	97279279	97279280	A	G	13	GENIC	homozygous	128664488
8	97279291	97279292	A		13	GENIC	homozygous	128618688
8	97279295	97279296	A		13	GENIC	homozygous	128618689
8	97279300	97279304	CATA		13	GENIC	homozygous	128618690
8	97279307	97279308	C		14	GENIC	homozygous	128618691
8	97279315	97279316	A	C	15	GENIC	homozygous	130374208
8	97279328	97279329	C	T	15	GENIC	homozygous	130374209
8	97279332	97279335	ATA		15	GENIC	homozygous	130366186
8	97279310	97279313	AGA		15	GENIC	homozygous	128618692
8	97279320	97279321	G		15	GENIC	homozygous	130366184
8	97279327	97279328	A		15	GENIC	homozygous	130366185
8	97279338	97279340	AA		15	GENIC	homozygous	130366187
8	97279342	97279343	C		15	GENIC	homozygous	130366188
8	97279350	97279353	AAC		16	GENIC	homozygous	130366189
8	97283301	97283301		C	2	GENIC	homozygous	128618701
8	97283408	97283409	G		11	GENIC	homozygous	128618702
8	97298838	97298839	T	A	7	GENIC	homozygous	116591956
8	97298840	97298841	C	T	7	GENIC	homozygous	116591958
8	97304323	97304323		G	12	GENIC	homozygous	130366191
8	97304430	97304433	GGG		20	GENIC	homozygous	128618704
8	97320393	97320394	C	A	7	GENIC	possibly homozygous	117054606
8	97360841	97360841		CA	20	GENIC	homozygous	128618713
8	97362616	97362617	G	A	2	GENIC	homozygous	116855353
8	97366167	97366169	TC		2	GENIC	homozygous	128618718
8	97368949	97368950	A	T	11	GENIC	homozygous	116592094
8	97369139	97369139		CT	18	GENIC	homozygous	128618719
8	97303563	97303563		AGAC	12	GENIC	heterozygous	130568215
8	97303550	97303551	G	C	11	GENIC	heterozygous	130570665
8	97303553	97303557	AAAC		12	GENIC	heterozygous	130568214