chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	84052053	84052054	A	G	21	GENIC	homozygous	116069109
11	84052055	84052056	G	A	22	GENIC	homozygous	116069111
11	84052186	84052187	A	G	20	GENIC	homozygous	116069113
11	84056006	84056007	G	T	18	GENIC	homozygous	116069115
11	84056471	84056472	C	T	22	GENIC	homozygous	116069117
11	84057438	84057439	G	T	14	GENIC	homozygous	116069119
11	84059005	84059006	A	G	18	GENIC	homozygous	116069121
11	84059268	84059269	G	A	16	GENIC	homozygous	116069123
11	84059340	84059341	G	A	23	GENIC	homozygous	116069125
11	84060009	84060010	A	G	21	GENIC	homozygous	116069127
11	84060222	84060223	C	A	15	GENIC	homozygous	116069129
11	84061264	84061265	G	A	8	GENIC	homozygous	116069131
11	84061921	84061922	G	A	13	GENIC	homozygous	116069133
11	84062979	84062980	C	T	21	GENIC	homozygous	116069141
11	84063578	84063579	A	G	18	GENIC	homozygous	116069143
11	84065405	84065406	C	T	15	GENIC	homozygous	116069145
11	84065610	84065611	T	C	23	GENIC	homozygous	116069147
11	84066408	84066409	C	T	30	GENIC	homozygous	116069149
11	84067080	84067081	A	G	7	GENIC	homozygous	116069151
11	84067398	84067399	A	T	17	GENIC	homozygous	116069153