chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	124662792	124662793	A	C	19	GENIC	homozygous	112825682
4	124662970	124662971	T	G	25	GENIC	homozygous	112825684
4	124663020	124663021	C	T	26	GENIC	homozygous	112825686
4	124663384	124663385	T	G	11	GENIC	homozygous	112825688
4	124684203	124684204	G	A	26	GENIC	homozygous	113241135
4	124692603	124692604	T	C	22	GENIC	homozygous	112825690
4	124719297	124719298	G	T	5	GENIC	homozygous	112825694
4	124719750	124719751	G	T	29	GENIC	possibly homozygous	112825696
4	124719902	124719903	G	T	3	GENIC	homozygous	113049467
4	124720163	124720164	C	A	11	GENIC	homozygous	112825698
4	124722112	124722113	C	A	20	GENIC	homozygous	112825700
4	124747563	124747564	C	G	16	GENIC	homozygous	112825704
4	124747568	124747569	A	G	17	GENIC	homozygous	112825706
4	124747578	124747579	C	A	21	GENIC	homozygous	112825708
4	124747607	124747608	G	T	23	GENIC	homozygous	112825710
4	124747613	124747614	G	C	27	GENIC	homozygous	112825712
4	124747620	124747621	T	C	30	GENIC	homozygous	112825714
4	124762735	124762736	A	T	15	GENIC	homozygous	112825716
4	124762894	124762895	G	C	12	GENIC	homozygous	112825718
4	124763170	124763171	C	A	12	GENIC	homozygous	112825720
4	124763229	124763230	A	C	11	GENIC	homozygous	112825726
4	124770642	124770643	T	A	22	GENIC	homozygous	112825728
4	124822393	124822394	C	G	18	GENIC	homozygous	113156093
4	124822417	124822418	A	G	17	GENIC	homozygous	113156094
4	124846025	124846026	C	G	2	GENIC	homozygous	112825740
4	124858273	124858274	G	C	21	GENIC	homozygous	112825742
4	124858276	124858277	T	C	21	GENIC	homozygous	112825744