chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	161451104	161451105	T	C	19	GENIC	homozygous	137661717
5	161451330	161451331	C		5	GENIC	homozygous	137351852
5	161451401	161451402	A	G	16	GENIC	homozygous	137661718
5	161451406	161451407	T	G	17	GENIC	homozygous	137661719
5	161451447	161451449	CG		21	GENIC	homozygous	137351853
5	161451450	161451455	CCGAC		21	GENIC	homozygous	137351854
5	161451470	161451471	C	T	20	GENIC	homozygous	137661720
5	161451599	161451600	T	C	16	GENIC	homozygous	137661721
5	161451648	161451649	C	T	15	GENIC	homozygous	137661722
5	161451875	161451876	T	C	9	GENIC	homozygous	137661723
5	161452470	161452471	A	T	12	GENIC	possibly homozygous	403164860
5	161451452	161451453	G	A	21	GENIC	heterozygous	154254622
5	161451452	161451453	G		21	GENIC	homozygous	403997406
5	161452466	161452467	A		12	GENIC	heterozygous	403164855
5	161452466	161452467	A	T	12	GENIC	possibly homozygous	403164856
5	161452468	161452469	A		12	GENIC	heterozygous	403164857
5	161452468	161452469	A	T	12	GENIC	possibly homozygous	403164858
5	161452470	161452471	A		12	GENIC	heterozygous	403164859
5	161452744	161452745	C	G	16	GENIC	homozygous	137661724
5	161453002	161453003	C	T	16	GENIC	homozygous	137661725
5	161453098	161453099	T	G	16	GENIC	homozygous	137661726
5	161453546	161453547	G	C	19	GENIC	homozygous	137661727
5	161453743	161453744	T	G	23	GENIC	homozygous	137661728
5	161454013	161454013		T	11	GENIC	homozygous	137351855
5	161454827	161454828	T	C	16	GENIC	homozygous	137661729
5	161454886	161454887	G	T	17	GENIC	homozygous	137661730
5	161454890	161454891	T	G	18	GENIC	homozygous	137661731
5	161455018	161455019	T	C	20	GENIC	homozygous	137661732
5	161455430	161455431	T	C	19	GENIC	homozygous	137661733