chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54246537	54246538	C	T	25	GENIC	homozygous	109733325
19	54246805	54246806	G	A	22	GENIC	homozygous	109733327
19	54246898	54246899	T	A	15	GENIC	homozygous	109733329
19	54247694	54247695	C	T	32	GENIC	homozygous	109733331
19	54248289	54248290	T	C	33	GENIC	homozygous	109733333
19	54248984	54248985	C	G	34	GENIC	homozygous	109733335
19	54249338	54249339	C	T	18	GENIC	homozygous	109890243
19	54249614	54249615	A	G	26	GENIC	homozygous	109733339
19	54249694	54249695	A	G	34	GENIC	homozygous	109733341
19	54249816	54249817	A	G	39	GENIC	homozygous	109733344
19	54250329	54250330	C	T	24	GENIC	homozygous	109733346
19	54250425	54250426	G	A	53	GENIC	heterozygous	109977694
19	54250438	54250439	A	G	54	GENIC	heterozygous	109977698
19	54250433	54250434	A	G	52	GENIC	homozygous	109825543
19	54251035	54251036	G	A	60	GENIC	heterozygous	119633261
19	54250528	54250529	C	T	52	GENIC	heterozygous	119633257
19	54250987	54250988	G	A	55	GENIC	heterozygous	119633258
19	54251000	54251001	A	G	54	GENIC	heterozygous	119633259
19	54251032	54251033	C	T	64	GENIC	heterozygous	119633260
19	54250952	54250953	G	A	26	GENIC	homozygous	109875891
19	54251036	54251037	C	T	60	GENIC	heterozygous	119633262
19	54251047	54251048	A	G	63	GENIC	heterozygous	119633263
19	54251125	54251126	T	A	34	GENIC	homozygous	109733348
19	54251783	54251784	C	T	31	GENIC	homozygous	109733350
19	54252022	54252023	G	A	43	GENIC	heterozygous	109733352
19	54252120	54252121	T	C	34	GENIC	heterozygous	109733354