chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	49330656	49330657	T	C	41	GENIC	homozygous	115348885
12	49330802	49330803	T	C	36	GENIC	homozygous	115348887
12	49331002	49331003	G	A	37	GENIC	homozygous	115348889
12	49331099	49331100	A	C	36	GENIC	homozygous	115348891
12	49331242	49331243	T	C	46	GENIC	homozygous	115348893
12	49331924	49331925	C	T	43	GENIC	homozygous	115348895
12	49332445	49332446	C	T	25	GENIC	homozygous	115348897
12	49333270	49333271	A	C	42	GENIC	homozygous	115348899
12	49333996	49333997	A	G	61	GENIC	homozygous	115348901
12	49334432	49334433	C	G	43	GENIC	homozygous	115348903
12	49334857	49334858	G	A	14	GENIC	homozygous	115348905
12	49335350	49335351	T	G	63	GENIC	homozygous	115348907
12	49336497	49336498	T	C	49	GENIC	homozygous	115348909
12	49336851	49336852	C	T	52	GENIC	homozygous	115348911
12	49336852	49336853	A	G	53	GENIC	homozygous	115348913
12	49337448	49337449	A	G	32	GENIC	homozygous	115348915
12	49338137	49338138	G	T	47	GENIC	homozygous	115348917
12	49339394	49339395	G	C	32	GENIC	homozygous	115348919
12	49339446	49339447	C	G	18	GENIC	homozygous	115348921
12	49340050	49340051	T	C	45	GENIC	homozygous	115348923
12	49341000	49341001	T	C	24	GENIC	homozygous	115348925
12	49341210	49341211	C	T	41	GENIC	homozygous	115348927
12	49373017	49373018	A	G	30	GENIC	homozygous	115348933
12	49369810	49369811	G	A	32	GENIC	homozygous	115348929
12	49372606	49372607	G	A	43	GENIC	homozygous	115348931
12	49376541	49376542	A	G	33	GENIC	possibly homozygous	115348935
12	49386849	49386850	A	G	34	GENIC	possibly homozygous	115348937