chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	4217736	4217737	G	A	16	GENIC	homozygous	50002749
12	4218375	4218377	AA	--	11	GENIC	homozygous	50002751
12	4218859	4218860	T	C	30	GENIC	homozygous	50002753
12	4218980	4218981	T	G	29	GENIC	homozygous	50002754
12	4220091	4220092	C	CT	11	GENIC	heterozygous	50526402
12	4222266	4222267	C	T	29	GENIC	homozygous	50002756
12	4223430	4223432	AG	--	5	GENIC	heterozygous	50002759
12	4223480	4223481	A	G	12	GENIC	homozygous	50002761
12	4224870	4224871	A	G	24	GENIC	homozygous	50002762
12	4226353	4226354	A	G	25	GENIC	homozygous	50002763
12	4226664	4226665	A	G	14	GENIC	homozygous	50002764
12	4228269	4228270	T	C	21	GENIC	homozygous	50002766
12	4228283	4228284	A	G	19	GENIC	homozygous	50002767
12	4228666	4228688	TGTGTGTGTATGTGTGTGTGTG	----------------------	6	GENIC	heterozygous	50526408
12	4228668	4228688	TGTGTGTATGTGTGTGTGTG	--------------------	6	GENIC	heterozygous	50526410
12	4229356	4229357	A	G	16	GENIC	homozygous	50002792
12	4229397	4229398	C	T	18	GENIC	homozygous	50002793
12	4229682	4229686	ACAC	----	3	GENIC	homozygous	50002795
12	4229985	4229986	A	T	16	GENIC	homozygous	50274550
12	4229986	4229987	T	C	15	GENIC	homozygous	50274552