chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	124676502	124676503	C	T	21	GENIC	homozygous	111694727
3	124676543	124676544	T		22	GENIC	homozygous	127926386
3	124676553	124676554	G		22	GENIC	homozygous	127926387
3	124676561	124676561		TT	20	GENIC	homozygous	127926388
3	124676576	124676576		GA	16	GENIC	homozygous	127926389
3	124683914	124683915	C	A	15	GENIC	homozygous	111694732
3	124683919	124683920	T	C	15	GENIC	homozygous	111694733
3	124683952	124683953	T	A	18	GENIC	homozygous	111694735
3	124683964	124683965	G	A	17	GENIC	homozygous	111694736
3	124683973	124683974	A		20	GENIC	homozygous	127926390
3	124683997	124683998	A		22	GENIC	homozygous	127926391
3	124684042	124684043	A		23	GENIC	homozygous	127926392
3	124684044	124684045	T	G	23	GENIC	homozygous	119938898
3	124684048	124684049	T		23	GENIC	homozygous	127926393
3	124684060	124684061	A	G	21	GENIC	homozygous	111694738
3	124684077	124684078	A	G	16	GENIC	homozygous	111694740
3	124684081	124684082	C	T	16	GENIC	homozygous	111694741
3	124684087	124684088	T	C	15	GENIC	homozygous	111694743
3	124785366	124785367	C	A	17	GENIC	homozygous	111694761
3	124793892	124793893	T	C	11	GENIC	heterozygous	112027729
3	124684053	124684053		A	23	GENIC	homozygous	127926394
3	124781032	124781034	AC		13	GENIC	heterozygous	130283053