chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	25079709	25079710	C	T	20	GENIC	homozygous	109866748
19	25080069	25080070	G	A	12	GENIC	homozygous	109866750
19	25081930	25081931	A	G	19	GENIC	homozygous	109866752
19	25081948	25081949	A	G	13	GENIC	homozygous	109672176
19	25082118	25082119	A	G	24	GENIC	homozygous	119602462
19	25082874	25082875	C	T	18	GENIC	homozygous	109866754
19	25084388	25084389	T	C	20	GENIC	homozygous	109866756
19	25084653	25084654	G	T	12	GENIC	homozygous	109866758
19	25088411	25088412	G	C	21	GENIC	homozygous	109672180
19	25089490	25089491	C	A	18	GENIC	homozygous	119678162
19	25089749	25089750	T	C	33	GENIC	homozygous	109672184
19	25089846	25089847	C	G	40	GENIC	homozygous	109866760
19	25090339	25090340	C	T	23	GENIC	homozygous	109866762
19	25090369	25090370	T	A	17	GENIC	homozygous	109866764
19	25090871	25090872	C	T	26	GENIC	homozygous	109866766
19	25091077	25091078	C	A	26	GENIC	homozygous	109866768
19	25091108	25091109	T	C	19	GENIC	homozygous	109866770
19	25091381	25091382	G	C	21	GENIC	homozygous	109672188
19	25091403	25091404	G	C	16	GENIC	homozygous	109672190
19	25091411	25091412	A	T	17	GENIC	homozygous	109672192