chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25038120	25038121	G	A	12	GENIC	homozygous	115369038
12	25038168	25038169	G	T	19	GENIC	homozygous	115369040
12	25038197	25038198	T	C	10	GENIC	homozygous	115369042
12	25038210	25038211	C	T	12	GENIC	homozygous	115369044
12	25039002	25039003	C	T	13	GENIC	homozygous	115289394
12	25040407	25040408	A	G	11	GENIC	homozygous	115289396
12	25044081	25044082	A	G	16	GENIC	homozygous	115289412
12	25044164	25044165	A	G	10	GENIC	homozygous	115289414
12	25044495	25044496	G	A	24	GENIC	homozygous	115369048
12	25045155	25045156	A	G	6	GENIC	homozygous	115289416
12	25045685	25045686	C	T	11	GENIC	homozygous	115369050
12	25048280	25048281	T	C	14	GENIC	homozygous	115369052
12	25048416	25048417	G	T	8	GENIC	homozygous	115289430
12	25049493	25049494	G	A	10	GENIC	homozygous	115369054
12	25050273	25050274	G	A	4	GENIC	heterozygous	126170934
12	25050488	25050489	C	T	5	GENIC	homozygous	115369056
12	25050498	25050499	G	C	6	GENIC	homozygous	115369058
12	25050812	25050813	C	T	19	GENIC	homozygous	115369060
12	25051245	25051246	G	A	17	GENIC	homozygous	115369062
12	25054317	25054318	C	A	7	GENIC	homozygous	115369064
12	25056897	25056898	A	G	11	GENIC	homozygous	115289447
12	25061602	25061603	G	A	15	GENIC	heterozygous	115369066
12	25062206	25062207	G	A	9	GENIC	homozygous	115369068
12	25064646	25064647	G	A	3	GENIC	heterozygous	118325055
12	25065812	25065813	C	A	14	GENIC	homozygous	115289489
12	25066487	25066488	C	T	15	GENIC	homozygous	115289493