chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	79181991	79181992	G	A	7	GENIC	homozygous	108873838
1	79182107	79182108	C	A	13	GENIC	homozygous	108873839
1	79184791	79184792	T	C	12	GENIC	homozygous	108873843
1	79182347	79182348	G	T	7	GENIC	homozygous	108873840
1	79182450	79182451	T	C	16	GENIC	homozygous	108873841
1	79182938	79182939	G	A	15	GENIC	homozygous	108873842
1	79184818	79184819	T	A	13	GENIC	homozygous	108873844
1	79185160	79185161	C	G	9	GENIC	homozygous	108873845
1	79185391	79185392	T	A	11	GENIC	homozygous	108873846
1	79185421	79185422	T	C	8	GENIC	homozygous	108873847
1	79185529	79185530	T	C	13	GENIC	homozygous	108873848
1	79185698	79185699	C	T	14	GENIC	homozygous	108873849
1	79186037	79186038	T	C	11	GENIC	homozygous	108873850
1	79186871	79186872	T	C	10	GENIC	homozygous	108873852
1	79187493	79187494	T	C	5	GENIC	homozygous	108873853
1	79187865	79187866	G	C	16	GENIC	homozygous	108873854
1	79188030	79188031	A	G	8	GENIC	homozygous	108873855
1	79188871	79188872	A	T	15	GENIC	homozygous	108873857
1	79188985	79188986	C	T	11	GENIC	homozygous	108873858
1	79188988	79188989	C	T	12	GENIC	homozygous	108873859
1	79190631	79190632	G	A	8	GENIC	homozygous	108873860