chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41215922	41215923	C	T	17	GENIC	homozygous	115583257
12	41216025	41216026	G	A	18	GENIC	homozygous	115384753
12	41216158	41216159	G	A	15	GENIC	homozygous	115384755
12	41216226	41216227	A	G	20	GENIC	possibly homozygous	115384759
12	41216283	41216284	G	A	36	GENIC	possibly homozygous	115384761
12	41216339	41216340	A	G	41	GENIC	homozygous	115384763
12	41216351	41216352	T	C	45	GENIC	homozygous	115384765
12	41216435	41216436	T	C	26	GENIC	homozygous	115451504
12	41216475	41216476	A	G	19	GENIC	homozygous	115329650
12	41216482	41216483	T	C	18	GENIC	homozygous	115384767
12	41216545	41216546	A	G	21	GENIC	homozygous	115384769
12	41216783	41216784	C	T	20	GENIC	possibly homozygous	115329654
12	41216806	41216807	G	A	22	GENIC	possibly homozygous	115384771
12	41216901	41216902	A	T	39	GENIC	possibly homozygous	115384773
12	41216928	41216929	A	G	38	GENIC	possibly homozygous	115384775
12	41216929	41216930	T	C	39	GENIC	possibly homozygous	115384777
12	41216957	41216958	T	G	40	GENIC	homozygous	115384779
12	41217041	41217042	G	T	29	GENIC	homozygous	115384781
12	41217061	41217062	T	C	34	GENIC	homozygous	115384783
12	41217146	41217147	T	G	29	GENIC	homozygous	115329656
12	41217227	41217228	T	C	30	GENIC	homozygous	115441901
12	41217332	41217333	T	C	11	GENIC	homozygous	115583259
12	41218122	41218123	A	G	15	GENIC	homozygous	115329664
12	41218201	41218202	G	A	22	GENIC	homozygous	115384785
12	41218335	41218336	A	G	18	GENIC	homozygous	115505816
12	41219702	41219703	A	G	18	GENIC	homozygous	115384787
12	41220597	41220598	A	G	18	GENIC	homozygous	115583261
12	41222216	41222217	A	G	43	GENIC	heterozygous	115329680
12	41222222	41222223	C	T	42	GENIC	heterozygous	115329682
12	41222223	41222224	A	G	42	GENIC	heterozygous	115329684
12	41222224	41222225	C	T	41	GENIC	heterozygous	115329686
12	41222237	41222238	A	C	40	GENIC	heterozygous	115329688
12	41222275	41222276	G	T	35	GENIC	heterozygous	115329690