chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	84043905	84043906	T	C	22	GENIC	homozygous	109305099
1	84043964	84043965	T	C	36	GENIC	possibly homozygous	109305101
1	84044249	84044250	G	A	17	GENIC	homozygous	109305103
1	84046681	84046682	T	A	32	GENIC	homozygous	108879924
1	84046969	84046970	T	C	38	GENIC	homozygous	108879925
1	84047340	84047341	C	T	28	GENIC	homozygous	108879927
1	84047532	84047533	T	C	24	GENIC	homozygous	108879928
1	84047644	84047645	A	G	9	GENIC	homozygous	108879929
1	84048095	84048096	G	C	22	GENIC	homozygous	109305105
1	84048115	84048116	C	T	22	GENIC	homozygous	109305108
1	84050037	84050038	A	G	10	GENIC	homozygous	109561283
1	84050964	84050965	A	G	48	GENIC	homozygous	108879934
1	84051929	84051930	T	C	36	GENIC	homozygous	108879935
1	84053097	84053098	A	G	33	GENIC	homozygous	108879936
1	84053677	84053678	G	A	23	GENIC	possibly homozygous	109305112
1	84053790	84053791	G	A	26	GENIC	possibly homozygous	109305114
1	84053832	84053833	A	C	25	GENIC	homozygous	108879938
1	84055996	84055997	T	G	15	GENIC	homozygous	108879940
1	84056507	84056508	A	T	21	GENIC	possibly homozygous	108879941
1	84056898	84056899	A	G	15	GENIC	homozygous	108879942
1	84057439	84057440	G	T	43	GENIC	homozygous	108879943
1	84058062	84058063	A	T	19	GENIC	homozygous	108879944
1	84058641	84058642	A	G	33	GENIC	homozygous	108879945
1	84058775	84058776	G	A	39	GENIC	homozygous	108879946
1	84059552	84059553	A	G	39	GENIC	homozygous	108879947
1	84060364	84060365	A	G	29	GENIC	homozygous	108879948
1	84061062	84061063	A	G	28	GENIC	homozygous	108879949
1	84062197	84062198	G	A	27	GENIC	homozygous	109305116
1	84062217	84062218	A	G	28	GENIC	homozygous	108879950
1	84062333	84062334	C	T	15	GENIC	homozygous	108879952
1	84063005	84063006	C	T	42	GENIC	homozygous	108879953
1	84063841	84063842	A	C	39	GENIC	homozygous	108879954