chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	26031412	26031413	T	C	60	GENIC	possibly homozygous	109776653
19	26031966	26031967	A	C	54	GENIC	possibly homozygous	109673579
19	26033859	26033860	C	G	23	GENIC	heterozygous	119602576
19	26037654	26037655	T	C	53	GENIC	homozygous	109673581
19	26037998	26037999	G	C	49	GENIC	homozygous	109673583
19	26039540	26039541	C	T	51	GENIC	homozygous	109673585
19	26042129	26042130	T	C	47	GENIC	possibly homozygous	109803245
19	26042606	26042607	G	A	46	GENIC	heterozygous	119639289
19	26044593	26044594	T	C	62	GENIC	possibly homozygous	109673587
19	26046276	26046277	T	C	55	GENIC	homozygous	109673589
19	26047360	26047361	C	T	61	GENIC	heterozygous	119639290
19	26047366	26047367	C	A	72	GENIC	heterozygous	119639291
19	26047414	26047415	C	T	97	GENIC	heterozygous	119639292
19	26047416	26047417	A	C	89	GENIC	heterozygous	119639293
19	26047460	26047461	C	T	58	GENIC	heterozygous	119639294
19	26047661	26047662	G	A	45	GENIC	homozygous	109673591
19	26050915	26050916	T	C	48	GENIC	homozygous	109673593
19	26051251	26051252	T	G	64	GENIC	possibly homozygous	109673595
19	26053368	26053369	A	G	33	GENIC	possibly homozygous	109803247