chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	127638556	127638557	G	A	31	GENIC	homozygous	111119524
2	127655866	127655867	A	G	13	GENIC	homozygous	110008779
2	127659782	127659783	C	G	27	GENIC	homozygous	111119528
2	127660332	127660333	A	G	15	GENIC	homozygous	111119530
2	127661296	127661297	T	C	28	GENIC	homozygous	111119532
2	127661425	127661426	T	C	40	GENIC	homozygous	110008785
2	127662455	127662456	A	G	14	GENIC	homozygous	111119536
2	127662729	127662730	G	A	20	GENIC	homozygous	111119538
2	127663723	127663724	A	C	21	GENIC	homozygous	111119540
2	127665270	127665271	G	A	34	GENIC	homozygous	111119542
2	127666753	127666754	A	C	24	GENIC	homozygous	110008788
2	127667044	127667045	T	C	17	GENIC	possibly homozygous	111119544
2	127667391	127667392	T	C	16	GENIC	homozygous	110008789
2	127667464	127667465	A	G	10	GENIC	homozygous	111119546
2	127667510	127667511	G	T	14	GENIC	homozygous	110008790
2	127670074	127670075	T	C	16	GENIC	homozygous	111119548
2	127670143	127670144	A	T	15	GENIC	homozygous	111119550
2	127670955	127670956	A	G	25	GENIC	homozygous	110008792
2	127674167	127674168	T	C	21	GENIC	homozygous	110008795
2	127674168	127674169	A	G	21	GENIC	homozygous	110008796
2	127679155	127679156	A	T	24	GENIC	homozygous	110008799
2	127679889	127679890	C	T	17	GENIC	homozygous	111119559
2	127680005	127680006	G	A	20	GENIC	homozygous	111119561
2	127680610	127680611	A	G	35	GENIC	homozygous	111119563