chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	108892487	108892488	T	C	46	GENIC	homozygous	112642703
15	108893582	108893583	T	C	24	GENIC	homozygous	112642705
15	108893674	108893675	C	T	39	GENIC	homozygous	112642707
15	108893765	108893766	A	C	27	GENIC	homozygous	112642709
15	108894621	108894622	T	C	33	GENIC	homozygous	112642711
15	108895108	108895109	T	C	43	GENIC	possibly homozygous	112642713
15	108895471	108895472	T	C	59	GENIC	homozygous	112642715
15	108895977	108895978	T	C	51	GENIC	homozygous	112642717
15	108896318	108896319	G	A	57	GENIC	homozygous	112642719
15	108896716	108896717	A	G	23	GENIC	homozygous	112642721
15	108896808	108896809	G	A	31	GENIC	homozygous	112642723
15	108896810	108896811	G	A	28	GENIC	homozygous	112642725
15	108898766	108898767	A	G	38	GENIC	homozygous	112642727
15	108898891	108898892	A	G	32	GENIC	homozygous	112642730
15	108899054	108899055	T	C	49	GENIC	homozygous	112642732
15	108899535	108899536	G	A	30	GENIC	homozygous	112642734
15	108901061	108901062	A	T	58	GENIC	homozygous	112642736
15	108901212	108901213	G	A	46	GENIC	homozygous	112642738
15	108901824	108901825	T	G	33	GENIC	homozygous	112642739
15	108902540	108902541	C	A	33	GENIC	homozygous	112642741
15	108902925	108902926	T	C	20	GENIC	homozygous	112642743
15	108904357	108904358	A	G	28	GENIC	homozygous	112642745
15	108905657	108905658	T	C	37	GENIC	homozygous	112642748
15	108906724	108906725	A	G	33	GENIC	homozygous	112642750
15	108907099	108907100	G	C	23	GENIC	homozygous	112642752
15	108907289	108907290	A	G	12	GENIC	homozygous	112642754