chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	108892487	108892488	T	C	31	GENIC	homozygous	112642703
15	108893582	108893583	T	C	18	GENIC	homozygous	112642705
15	108893674	108893675	C	T	19	GENIC	homozygous	112642707
15	108893964	108893965	C	T	21	GENIC	homozygous	112865621
15	108894621	108894622	T	C	26	GENIC	homozygous	112642711
15	108895108	108895109	T	C	20	GENIC	homozygous	112642713
15	108895471	108895472	T	C	36	GENIC	homozygous	112642715
15	108895977	108895978	T	C	44	GENIC	homozygous	112642717
15	108896716	108896717	A	G	29	GENIC	homozygous	112642721
15	108898766	108898767	A	G	26	GENIC	homozygous	112642727
15	108898891	108898892	A	G	39	GENIC	homozygous	112642730
15	108899054	108899055	T	C	27	GENIC	homozygous	112642732
15	108899535	108899536	G	A	10	GENIC	homozygous	112642734
15	108901061	108901062	A	T	14	GENIC	homozygous	112642736
15	108901355	108901356	C	T	33	GENIC	homozygous	112865623
15	108901824	108901825	T	G	21	GENIC	homozygous	112642739
15	108902538	108902539	C	A	36	GENIC	homozygous	112865625
15	108902540	108902541	C	A	36	GENIC	homozygous	112642741
15	108904357	108904358	A	G	27	GENIC	homozygous	112642745
15	108904397	108904398	G	T	26	GENIC	homozygous	112865627
15	108904689	108904690	G	T	28	GENIC	homozygous	112865629
15	108905657	108905658	T	C	30	GENIC	homozygous	112642748
15	108906724	108906725	A	G	37	GENIC	homozygous	112642750
15	108907099	108907100	G	C	25	GENIC	homozygous	112642752
15	108905076	108905077	C	A	17	GENIC	homozygous	113013397
15	108904916	108904917	C	G	28	GENIC	homozygous	113013395