chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23790401	23790402	C	T	10	GENIC	homozygous	115368652
12	23790437	23790438	T	C	15	GENIC	homozygous	115285810
12	23790859	23790860	T	A	15	GENIC	homozygous	115368654
12	23791151	23791152	T	C	28	GENIC	homozygous	115285814
12	23791813	23791814	G	A	16	GENIC	homozygous	115285816
12	23792559	23792560	G	A	25	GENIC	homozygous	115368656
12	23793477	23793478	A	T	29	GENIC	homozygous	115285818
12	23795054	23795055	A	G	31	GENIC	homozygous	115368658
12	23796333	23796334	T	C	39	GENIC	homozygous	115285826
12	23798920	23798921	G	A	29	GENIC	homozygous	115368660
12	23799910	23799911	G	A	22	GENIC	homozygous	115368662
12	23800087	23800088	T	A	21	GENIC	homozygous	115285834
12	23800247	23800248	C	G	22	GENIC	homozygous	115368664
12	23800317	23800318	C	T	22	GENIC	homozygous	115285838
12	23801574	23801575	A	G	23	GENIC	homozygous	115285844
12	23803532	23803533	G	A	27	GENIC	homozygous	115368666
12	23803753	23803754	A	G	37	GENIC	homozygous	115368668
12	23804555	23804556	T	C	23	GENIC	homozygous	115368670
12	23806124	23806125	A	T	29	GENIC	homozygous	115285852
12	23810713	23810714	T	G	18	GENIC	homozygous	115368672
12	23811773	23811774	C	T	35	GENIC	homozygous	115285876