chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54246537	54246538	C	T	49	GENIC	homozygous	109733325
19	54246805	54246806	G	A	51	GENIC	homozygous	109733327
19	54246898	54246899	T	A	40	GENIC	homozygous	109733329
19	54247694	54247695	C	T	49	GENIC	homozygous	109733331
19	54248289	54248290	T	C	49	GENIC	homozygous	109733333
19	54248984	54248985	C	G	54	GENIC	homozygous	109733335
19	54249361	54249362	G	A	44	GENIC	homozygous	109733337
19	54249614	54249615	A	G	47	GENIC	homozygous	109733339
19	54249694	54249695	A	G	42	GENIC	homozygous	109733341
19	54249816	54249817	A	G	40	GENIC	homozygous	109733344
19	54250329	54250330	C	T	48	GENIC	homozygous	109733346
19	54249192	54249196	GTAT		37	GENIC	homozygous	129622110
19	54249595	54249596	T		49	GENIC	homozygous	129622111
19	54249338	54249339	C	T	47	GENIC	homozygous	109890243
19	54250483	54250484	A	C	70	GENIC	heterozygous	109977701
19	54250484	54250485	G	A	70	GENIC	heterozygous	109977703
19	54250433	54250434	A	G	61	GENIC	homozygous	109825543
19	54250952	54250953	G	A	54	GENIC	homozygous	109875891
19	54251125	54251126	T	A	53	GENIC	homozygous	109733348
19	54251783	54251784	C	T	59	GENIC	homozygous	109733350
19	54252022	54252023	G	A	87	GENIC	heterozygous	109733352
19	54252119	54252119		CCC	52	GENIC	heterozygous	129622112