chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	89174709	89174710	T	C	27	GENIC	homozygous	111140270
17	89174906	89174906		A	26	GENIC	homozygous	129487566
17	89175447	89175448	T		24	GENIC	possibly homozygous	129487567
17	89177157	89177158	A	G	19	GENIC	homozygous	111140272
17	89184998	89184999	T	G	12	GENIC	homozygous	119309205
17	89187503	89187504	A	G	19	GENIC	homozygous	111140274
17	89191590	89191591	G	T	18	GENIC	homozygous	111140276
17	89191594	89191595	G	T	18	GENIC	homozygous	111140278
17	89191595	89191596	G	T	18	GENIC	homozygous	111140280
17	89191597	89191598	G	A	17	GENIC	homozygous	111140282
17	89191599	89191600	G		17	GENIC	homozygous	129487568
17	89191703	89191704	T	A	10	GENIC	heterozygous	124400621
17	89191705	89191706	T	A	10	GENIC	homozygous	124400622
17	89193341	89193342	T	C	17	GENIC	homozygous	111140286
17	89202144	89202145	A	G	21	GENIC	homozygous	111140288
17	89207082	89207083	A	G	18	GENIC	homozygous	111140290
17	89210100	89210101	A		21	GENIC	homozygous	129487570
17	89216179	89216182	TGT		14	GENIC	possibly homozygous	129487571
17	89219309	89219310	G	A	14	GENIC	homozygous	111140292
17	89224115	89224116	G	A	20	GENIC	homozygous	111140294
17	89229163	89229164	C	T	25	GENIC	homozygous	111140296
17	89232106	89232107	C	G	24	GENIC	homozygous	111140298