chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	150033958	150033959	T	C	21	GENIC	homozygous	114054667
5	150034287	150034288	A	G	40	GENIC	homozygous	114054669
5	150034347	150034348	A	G	31	GENIC	homozygous	114054670
5	150034367	150034368	A	G	34	GENIC	homozygous	114054672
5	150034561	150034562	G	A	35	GENIC	homozygous	114054674
5	150034749	150034750	C	T	31	GENIC	homozygous	114054676
5	150036681	150036682	A	G	23	GENIC	homozygous	114054678
5	150037426	150037427	A	C	17	GENIC	homozygous	114054680
5	150038106	150038107	T	C	18	GENIC	homozygous	114054682
5	150038978	150038979	G	A	22	GENIC	homozygous	114054684
5	150039488	150039489	A	G	15	GENIC	possibly homozygous	114054686
5	150039681	150039682	A	T	28	GENIC	homozygous	114054688
5	150040107	150040108	A	G	28	GENIC	homozygous	114054690
5	150040588	150040589	A	G	24	GENIC	homozygous	114054692
5	150041121	150041122	G	T	30	GENIC	homozygous	114054694
5	150043963	150043964	G	T	34	GENIC	homozygous	114054696
5	150045785	150045786	A	G	24	GENIC	homozygous	114054698
5	150046685	150046686	C	T	16	GENIC	homozygous	114054700
5	150050883	150050884	A	T	20	GENIC	homozygous	114054702
5	150051896	150051897	G	A	26	GENIC	homozygous	114054704
5	150054908	150054909	G	A	16	GENIC	homozygous	114054706
5	150054948	150054949	C	A	17	GENIC	possibly homozygous	114054708