chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	25183309	25183310	A	C	14	GENIC	homozygous	110064367
19	25184199	25184200	A	G	30	GENIC	homozygous	109672277
19	25184661	25184662	C	T	24	GENIC	possibly homozygous	109776348
19	25186211	25186212	T	C	31	GENIC	homozygous	109672279
19	25187090	25187091	A	G	32	GENIC	homozygous	109672281
19	25187942	25187943	A	G	27	GENIC	homozygous	109672283
19	25188035	25188036	C	A	18	GENIC	homozygous	109672285
19	25190400	25190401	C	T	24	GENIC	homozygous	109672289
19	25191343	25191344	A	G	18	GENIC	homozygous	109672291
19	25192802	25192803	A	T	20	GENIC	homozygous	109672293
19	25192852	25192853	A	G	15	GENIC	homozygous	109672295
19	25194614	25194615	T	C	30	GENIC	homozygous	109672297
19	25194876	25194877	A	G	42	GENIC	homozygous	109672300
19	25195694	25195695	C	T	37	GENIC	homozygous	109776350
19	25196847	25196848	A	G	34	GENIC	homozygous	109672302
19	25197942	25197943	C	T	26	GENIC	homozygous	109776352
19	25200043	25200044	G	A	30	GENIC	homozygous	109776354
19	25200832	25200833	C	T	12	GENIC	possibly homozygous	109776356
19	25201478	25201479	A	C	20	GENIC	heterozygous	109776361
19	25202002	25202003	A	G	31	GENIC	homozygous	109672306
19	25202451	25202452	T	C	27	GENIC	homozygous	109776363
19	25204227	25204228	T	C	38	GENIC	possibly homozygous	109672310
19	25204348	25204349	C	A	41	GENIC	heterozygous	119658113
19	25205629	25205630	T	C	25	GENIC	homozygous	109672314
19	25208930	25208931	T	A	26	GENIC	homozygous	109917483
19	25211398	25211399	C	T	40	GENIC	homozygous	109776365
19	25211948	25211949	T	C	19	GENIC	homozygous	109672316