chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	53572827	53572828	T	C	18	GENIC	homozygous	108851323
1	53573453	53573454	G	A	22	GENIC	homozygous	108098212
1	53573527	53573528	A	G	16	GENIC	homozygous	108098213
1	53573975	53573976	C	G	23	GENIC	homozygous	108098214
1	53574073	53574074	A	G	29	GENIC	homozygous	108098215
1	53574154	53574155	C	T	31	GENIC	homozygous	108098216
1	53574177	53574178	G	A	32	GENIC	homozygous	108098217
1	53574431	53574432	A	G	32	GENIC	homozygous	108098218
1	53574868	53574869	A	G	18	GENIC	homozygous	108098220
1	53575096	53575097	A	T	39	GENIC	possibly homozygous	108851324
1	53576605	53576606	A	G	15	GENIC	homozygous	108098229
1	53576669	53576670	A	G	20	GENIC	homozygous	108851325
1	53577240	53577241	T	C	27	GENIC	homozygous	108098230
1	53581048	53581049	C	T	23	GENIC	homozygous	108098234
1	53591313	53591314	A	C	22	GENIC	homozygous	108098248
1	53591424	53591425	G	A	18	GENIC	homozygous	108851327
1	53591895	53591896	C	A	25	GENIC	homozygous	108098252
1	53592513	53592514	T	G	33	GENIC	homozygous	108851328
1	53592527	53592528	T	C	34	GENIC	homozygous	108098253
1	53592641	53592642	C	G	34	GENIC	homozygous	108098254
1	53592760	53592761	T	C	40	GENIC	possibly homozygous	108098256
1	53593054	53593055	A	G	27	GENIC	homozygous	108851329
1	53593238	53593239	A	C	29	GENIC	homozygous	108098257