chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	26027923	26027941	TCTCTCTCTCTCTCTCTT		13	GENIC	heterozygous	129596211
19	26031368	26031368		TTTG	30	GENIC	possibly homozygous	129596212
19	26031412	26031413	T	C	41	GENIC	homozygous	109776653
19	26031966	26031967	A	C	30	GENIC	homozygous	109673579
19	26037654	26037655	T	C	46	GENIC	homozygous	109673581
19	26037998	26037999	G	C	49	GENIC	homozygous	109673583
19	26039540	26039541	C	T	37	GENIC	homozygous	109673585
19	26044593	26044594	T	C	60	GENIC	homozygous	109673587
19	26046276	26046277	T	C	47	GENIC	homozygous	109673589
19	26047661	26047662	G	A	30	GENIC	homozygous	109673591
19	26050915	26050916	T	C	47	GENIC	homozygous	109673593
19	26051251	26051252	T	G	36	GENIC	homozygous	109673595
19	26042129	26042130	T	C	21	GENIC	homozygous	109803245
19	26053368	26053369	A	G	39	GENIC	homozygous	109803247