chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	72897986	72897987	G	T	17	GENIC	homozygous	112711893
4	72898163	72898164	C	T	12	GENIC	homozygous	112711895
4	72898747	72898748	C	T	15	GENIC	homozygous	112711897
4	72898997	72898998	G	A	5	GENIC	homozygous	112711899
4	72899117	72899118	T	C	11	GENIC	homozygous	112711901
4	72899282	72899283	A	G	19	GENIC	homozygous	112711903
4	72901180	72901181	C	T	15	GENIC	homozygous	112711909
4	72901212	72901213	G	A	12	GENIC	homozygous	112711911
4	72902003	72902004	A	G	42	GENIC	homozygous	112711913
4	72902349	72902350	T	C	27	GENIC	homozygous	112711915
4	72903464	72903465	T	C	30	GENIC	homozygous	112711917
4	72904691	72904692	G	C	45	GENIC	possibly homozygous	112711921
4	72905029	72905030	G	C	40	GENIC	homozygous	112711923
4	72905901	72905902	A	G	38	GENIC	homozygous	112711925
4	72906205	72906206	G	A	26	GENIC	homozygous	112711929
4	72906472	72906473	A	G	26	GENIC	homozygous	112711931
4	72906837	72906838	T	A	25	GENIC	homozygous	112711935
4	72907566	72907567	G	T	15	GENIC	possibly homozygous	112711937
4	72909598	72909599	C	G	29	GENIC	homozygous	112711951
4	72910599	72910600	T	A	35	GENIC	homozygous	112711955
4	72910686	72910687	C	A	44	GENIC	homozygous	112711957
4	72910834	72910835	T	C	54	GENIC	homozygous	112711959
4	72910879	72910880	G	A	37	GENIC	homozygous	112711961
4	72911427	72911428	G	A	27	GENIC	homozygous	112711963
4	72911962	72911963	C	T	29	GENIC	homozygous	112711965