chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	93657094	93657095	T	C	21	GENIC	homozygous	109920692
2	93657263	93657264	G	A	35	GENIC	homozygous	110720468
2	93657397	93657398	T	C	35	GENIC	possibly homozygous	109920694
2	93658169	93658170	T	C	43	GENIC	homozygous	109920696
2	93658184	93658185	C	T	44	GENIC	homozygous	110720469
2	93658369	93658370	T	C	34	GENIC	homozygous	110720470
2	93659033	93659034	G	A	60	GENIC	homozygous	110720471
2	93659120	93659121	G	A	43	GENIC	homozygous	109920700
2	93659506	93659507	T	C	45	GENIC	homozygous	109920702
2	93659985	93659986	A	C	52	GENIC	homozygous	109920704
2	93660077	93660078	T	C	47	GENIC	homozygous	109920706
2	93660355	93660356	A	C	47	GENIC	homozygous	109920712
2	93660503	93660504	C	T	42	GENIC	homozygous	109920714
2	93660508	93660509	C	A	42	GENIC	homozygous	110720472
2	93660567	93660568	T	C	44	GENIC	homozygous	109920716
2	93661055	93661056	G	A	57	GENIC	possibly homozygous	110720473
2	93661352	93661353	G	A	57	GENIC	homozygous	109920717
2	93662303	93662304	T	C	57	GENIC	homozygous	109920719
2	93662333	93662334	C	A	52	GENIC	homozygous	110720474
2	93663549	93663550	C	T	42	GENIC	homozygous	109920723
2	93663887	93663888	G	A	51	GENIC	homozygous	110720475
2	93664120	93664121	G	T	51	GENIC	homozygous	110720476
2	93664417	93664418	A	G	38	GENIC	homozygous	109920731
2	93664691	93664692	A	T	49	GENIC	homozygous	109920733
2	93665098	93665099	G	C	26	GENIC	homozygous	109920739
2	93665191	93665192	G	T	33	GENIC	homozygous	109920741
2	93665236	93665237	G	A	40	GENIC	homozygous	109920743
2	93665241	93665242	A	T	35	GENIC	homozygous	110720477
2	93665685	93665686	T	C	43	GENIC	homozygous	109920745