chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	37368853	37368854	A	G	14	GENIC	homozygous	115380842
12	37371533	37371534	A	G	15	GENIC	homozygous	115380844
12	37373946	37373947	C	T	17	GENIC	possibly homozygous	115380846
12	37374396	37374397	G	T	20	GENIC	homozygous	115380848
12	37374844	37374845	A	G	24	GENIC	homozygous	115380850
12	37376312	37376313	G	C	23	GENIC	homozygous	115320306
12	37380494	37380495	T	C	29	GENIC	homozygous	115486174
12	37381905	37381906	G	A	29	GENIC	homozygous	115380852
12	37381910	37381911	T	C	27	GENIC	homozygous	115380854
12	37384618	37384619	C	G	25	GENIC	homozygous	115320310
12	37385385	37385386	A	C	32	GENIC	homozygous	115380856
12	37385820	37385821	A	G	19	GENIC	homozygous	115380858
12	37386324	37386325	T	C	23	GENIC	homozygous	115320312
12	37387201	37387202	T	C	29	GENIC	homozygous	115380860
12	37389149	37389150	A	G	16	GENIC	homozygous	115320316
12	37389786	37389787	C	T	18	GENIC	homozygous	115380862
12	37389858	37389859	C	T	24	GENIC	homozygous	115380864
12	37389967	37389968	T	G	25	GENIC	homozygous	115380866
12	37390056	37390057	A	G	27	GENIC	homozygous	115380868
12	37391786	37391787	C	T	19	GENIC	homozygous	115380870
12	37392191	37392192	C	T	23	GENIC	homozygous	115380872
12	37383167	37383168	G	A	26	GENIC	homozygous	115426308
12	37394853	37394854	G	A	16	GENIC	homozygous	115486175
12	37395108	37395109	A	C	17	GENIC	possibly homozygous	115380874
12	37395766	37395767	C	T	19	GENIC	homozygous	115380876
12	37396046	37396047	T	C	17	GENIC	homozygous	115380878
12	37396056	37396057	T	C	16	GENIC	homozygous	115380880
12	37396308	37396309	G	C	18	GENIC	homozygous	115380882
12	37396694	37396695	G	A	28	GENIC	possibly homozygous	115380884