chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10567304	10567305	G	C	38	GENIC	homozygous	110954352
17	10567961	10567962	G	A	23	GENIC	homozygous	110954354
17	10569857	10569858	T	C	36	GENIC	homozygous	110954356
17	10570724	10570725	G	A	24	GENIC	homozygous	110954358
17	10572251	10572252	A	G	26	GENIC	homozygous	110954360
17	10572288	10572289	C	G	26	GENIC	homozygous	110954362
17	10572381	10572382	C	T	20	GENIC	homozygous	110954364
17	10572435	10572436	C	T	21	GENIC	homozygous	110954366
17	10572641	10572642	T	C	20	GENIC	homozygous	110954368
17	10572858	10572859	A	T	18	GENIC	homozygous	110954370
17	10573122	10573123	G	T	19	GENIC	homozygous	110954372
17	10573639	10573640	G	A	15	GENIC	homozygous	110954374
17	10573798	10573799	T	G	11	GENIC	heterozygous	111402078
17	10573799	10573800	A	G	10	GENIC	heterozygous	111402079
17	10573801	10573802	T	G	11	GENIC	heterozygous	111402080
17	10574326	10574327	G	A	26	GENIC	homozygous	111231018