chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9601192	9601192		T	9	GENIC	homozygous	129657449
20	9601196	9601197	C		9	GENIC	homozygous	129657450
20	9601211	9601212	G		9	GENIC	homozygous	129657451
20	9601259	9601260	G		19	GENIC	homozygous	129657452
20	9601274	9601276	GG		17	GENIC	homozygous	129657453
20	9601292	9601292		G	15	GENIC	homozygous	129657454
20	9601321	9601322	G		9	GENIC	homozygous	129657455
20	9601342	9601342		T	9	GENIC	homozygous	129657456
20	9601351	9601352	A		7	GENIC	homozygous	129657457
20	9601358	9601359	T		6	GENIC	homozygous	129657458
20	9605239	9605240	G	A	29	GENIC	homozygous	109088511
20	9605293	9605293		C	27	GENIC	homozygous	129657462
20	9605357	9605357		A	22	GENIC	homozygous	129657463
20	9605363	9605363		C	23	GENIC	homozygous	129657464
20	9605460	9605460		C	25	GENIC	homozygous	129657466
20	9605464	9605464		A	25	GENIC	homozygous	129657467
20	9608281	9608282	C		17	GENIC	homozygous	129657468
20	9608313	9608314	C	G	17	GENIC	homozygous	109455842
20	9608315	9608316	C		16	GENIC	homozygous	129657469
20	9608318	9608319	C		16	GENIC	homozygous	129657470
20	9608324	9608325	G		16	GENIC	homozygous	129657471
20	9616644	9616645	G		28	GENIC	homozygous	129657478
20	9616780	9616781	A	G	36	GENIC	homozygous	109088603