chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	91581094	91581095	A	G	13	GENIC	homozygous	136215577
2	91581200	91581201	C	T	13	GENIC	homozygous	136215578
2	91581296	91581297	G		4	GENIC	homozygous	135927779
2	91581340	91581341	C	T	8	GENIC	homozygous	136215579
2	91582464	91582465	G	A	26	GENIC	homozygous	136215580
2	91582554	91582555	C	A	28	GENIC	homozygous	136215581
2	91583087	91583089	AT		28	GENIC	homozygous	135927780
2	91583179	91583180	A	G	33	GENIC	homozygous	136215582
2	91584100	91584101	T	C	16	GENIC	homozygous	136215583
2	91584113	91584114	T	C	17	GENIC	homozygous	136215584
2	91584451	91584452	T	C	7	GENIC	homozygous	136215585
2	91584459	91584460	G	C	7	GENIC	homozygous	136215586
2	91584462	91584463	T	C	7	GENIC	homozygous	136215587
2	91584469	91584470	T	C	3	GENIC	homozygous	136215588
2	91584773	91584774	T	C	15	GENIC	homozygous	136215590
2	91584918	91584919	G	A	14	GENIC	homozygous	136215591
2	91584860	91584861	T		17	GENIC	homozygous	403012181
2	91584906	91584907	T	C	17	GENIC	heterozygous	153959480
2	91584860	91584861	T	C	17	GENIC	heterozygous	403012182
2	91584865	91584866	C		17	GENIC	homozygous	403012183
2	91584865	91584866	C	T	17	GENIC	heterozygous	403012184
2	91584906	91584907	T		17	GENIC	homozygous	403012185