chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24349553	24349554	A	G	30	GENIC	homozygous	115287734
12	24350448	24350449	C	A	28	GENIC	possibly homozygous	115287736
12	24351627	24351628	G	A	44	GENIC	homozygous	115287738
12	24353414	24353415	A	G	46	GENIC	homozygous	115287740
12	24358661	24358662	T	C	25	GENIC	homozygous	115287742
12	24358782	24358783	A	G	31	GENIC	homozygous	115287744
12	24359415	24359416	C	G	34	GENIC	homozygous	115287746
12	24359591	24359592	G	A	41	GENIC	possibly homozygous	115287748
12	24359777	24359778	T	C	44	GENIC	homozygous	115287750
12	24360206	24360207	C	G	36	GENIC	homozygous	115287752
12	24361017	24361018	G	A	43	GENIC	homozygous	115287754
12	24361362	24361363	G	A	37	GENIC	homozygous	115287756
12	24361461	24361462	T	C	38	GENIC	homozygous	115287758
12	24363616	24363617	T	C	37	GENIC	homozygous	115287776
12	24358331	24358332	C	A	15	GENIC	possibly homozygous	118262083
12	24360005	24360006	T	C	20	GENIC	heterozygous	118337090
12	24361467	24361468	C	A	38	GENIC	homozygous	115287760
12	24361639	24361640	G	A	35	GENIC	homozygous	115287762
12	24362237	24362238	A	G	22	GENIC	homozygous	115287764
12	24362437	24362438	G	A	37	GENIC	homozygous	115287766
12	24362726	24362727	A	G	38	GENIC	homozygous	115287768
12	24363373	24363374	G	T	26	GENIC	possibly homozygous	115287772
12	24363548	24363549	A	T	40	GENIC	homozygous	115287774
12	24362133	24362134	T	C	40	GENIC	homozygous	115422206
12	24363788	24363789	A	G	39	GENIC	homozygous	115287778
12	24363897	24363898	T	C	32	GENIC	homozygous	115287780
12	24364055	24364056	A	T	17	GENIC	homozygous	118262084
12	24364215	24364216	C	T	36	GENIC	homozygous	115287782
12	24364276	24364277	C	T	37	GENIC	homozygous	115287784
12	24364277	24364278	C	T	38	GENIC	homozygous	115287786
12	24364523	24364524	A	G	29	GENIC	homozygous	115287788
12	24364749	24364750	T	G	44	GENIC	possibly homozygous	115287790
12	24365146	24365147	T	C	41	GENIC	homozygous	115287792
12	24365366	24365367	G	A	27	GENIC	homozygous	115287794