chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	22401513	22401514	A	G	26	GENIC	homozygous	115366664
12	22403426	22403427	T	A	12	GENIC	homozygous	115366666
12	22405602	22405603	A	G	18	GENIC	homozygous	115281441
12	22409242	22409243	T	G	20	GENIC	homozygous	115281447
12	22409243	22409244	T	C	21	GENIC	homozygous	115281449
12	22409510	22409511	G	A	16	GENIC	homozygous	115281451
12	22409573	22409574	G	A	13	GENIC	homozygous	115281453
12	22410433	22410434	A	G	16	GENIC	homozygous	115281455
12	22411637	22411638	G	C	25	GENIC	homozygous	115469521
12	22411853	22411854	G	A	15	GENIC	homozygous	115366668
12	22413339	22413340	C	T	29	GENIC	homozygous	115366670
12	22413662	22413663	T	C	14	GENIC	homozygous	115281461
12	22413864	22413865	A	G	17	GENIC	homozygous	115281463
12	22414051	22414052	T	C	27	GENIC	homozygous	115281467
12	22414961	22414962	A	T	17	GENIC	homozygous	115281469
12	22414988	22414989	C	T	18	GENIC	homozygous	115281471
12	22415039	22415040	C	G	12	GENIC	homozygous	115281473
12	22415999	22416000	A	G	15	GENIC	homozygous	115281475
12	22416473	22416474	G	T	16	GENIC	homozygous	115366672
12	22416482	22416483	G	T	14	GENIC	homozygous	115281477
12	22416805	22416806	T	C	22	GENIC	homozygous	115281479
12	22416825	22416826	C	A	21	GENIC	homozygous	115281481
12	22416938	22416939	C	A	20	GENIC	homozygous	115281483