chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	37368853	37368854	A	G	53	GENIC	homozygous	115380842
12	37368919	37368920	G	A	54	GENIC	homozygous	115565277
12	37369822	37369823	G	A	49	GENIC	homozygous	115565279
12	37374844	37374845	A	G	29	GENIC	homozygous	115380850
12	37375957	37375958	G	A	22	GENIC	homozygous	115565281
12	37381910	37381911	T	C	71	GENIC	homozygous	115380854
12	37376312	37376313	G	C	52	GENIC	homozygous	115320306
12	37377384	37377385	G	A	48	GENIC	homozygous	115608613
12	37380649	37380650	C	T	61	GENIC	homozygous	115608615
12	37381501	37381502	G	A	56	GENIC	homozygous	115608617
12	37381033	37381034	C	T	38	GENIC	homozygous	115622346
12	37381319	37381320	A	T	32	GENIC	homozygous	115622348
12	37385385	37385386	A	C	36	GENIC	homozygous	115380856
12	37385820	37385821	A	G	51	GENIC	homozygous	115380858
12	37386324	37386325	T	C	61	GENIC	homozygous	115320312
12	37388843	37388844	C	T	70	GENIC	homozygous	115608619
12	37389149	37389150	A	G	74	GENIC	homozygous	115320316
12	37389920	37389921	G	A	82	GENIC	homozygous	115608621
12	37389967	37389968	T	G	81	GENIC	homozygous	115380866
12	37390056	37390057	A	G	70	GENIC	homozygous	115380868
12	37391152	37391153	T	G	26	GENIC	possibly homozygous	115608623
12	37391761	37391762	G	A	44	GENIC	homozygous	115608625
12	37396046	37396047	T	C	19	GENIC	homozygous	115380878
12	37396056	37396057	T	C	17	GENIC	homozygous	115380880
12	37396308	37396309	G	C	34	GENIC	homozygous	115380882
12	37397607	37397608	C	T	45	GENIC	homozygous	115608627