chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	93575784	93575785	G	A	11	GENIC	homozygous	109920560
2	93580702	93580703	T	C	12	GENIC	homozygous	109920576
2	93581833	93581834	G	T	11	GENIC	homozygous	109920578
2	93582369	93582370	A	G	6	GENIC	homozygous	109920580
2	93582428	93582429	A	T	6	GENIC	homozygous	109920582
2	93582488	93582489	T	A	9	GENIC	homozygous	109920584
2	93582671	93582672	C	A	9	GENIC	homozygous	109920586
2	93582820	93582821	A	G	9	GENIC	homozygous	109920588
2	93583025	93583026	C	T	5	GENIC	homozygous	109920590
2	93583988	93583989	A	G	8	GENIC	homozygous	109920592
2	93584652	93584653	T	C	17	GENIC	homozygous	109920594
2	93584856	93584857	A	T	7	GENIC	homozygous	109920596
2	93590413	93590414	C	T	10	GENIC	homozygous	109920598
2	93597609	93597610	C	A	8	GENIC	homozygous	109920602
2	93626187	93626188	T	C	9	GENIC	homozygous	109920610
2	93631250	93631251	A	T	12	GENIC	homozygous	109920614
2	93631251	93631252	G	T	12	GENIC	homozygous	109920616
2	93631718	93631719	G	A	10	GENIC	homozygous	109920618
2	93637458	93637459	T	C	14	GENIC	homozygous	109920627
2	93639259	93639260	C	T	18	GENIC	homozygous	109920633
2	93641282	93641283	T	G	7	GENIC	homozygous	109920635