chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	9727714	9727715	T	A	50	GENIC	homozygous	112065341
3	9728124	9728125	C	T	61	GENIC	homozygous	112065343
3	9728584	9728585	G	A	46	GENIC	homozygous	112065345
3	9728756	9728757	C	A	40	GENIC	possibly homozygous	112065347
3	9729209	9729210	G		44	GENIC	homozygous	132038424
3	9730233	9730234	A	G	28	GENIC	homozygous	112065349
3	9730259	9730261	AC		26	GENIC	homozygous	132038425
3	9730265	9730267	AC		25	GENIC	homozygous	132038426
3	9730271	9730273	AC		25	GENIC	homozygous	132038427
3	9730441	9730442	T	C	49	GENIC	homozygous	112065351
3	9730636	9730637	G	A	43	GENIC	homozygous	112065353
3	9730789	9730790	A	G	40	GENIC	homozygous	112065355
3	9731842	9731843	T	C	58	GENIC	possibly homozygous	112065357
3	9731915	9731916	G	A	62	GENIC	homozygous	112065359
3	9732530	9732531	A	C	48	GENIC	homozygous	112065361
3	9732938	9732939	G	A	44	GENIC	homozygous	112065363
3	9733981	9733982	C	A	49	GENIC	homozygous	112065365
3	9733982	9733983	C	T	49	GENIC	homozygous	112065367
3	9734186	9734187	C	T	32	GENIC	homozygous	112065369
3	9734218	9734219	C	T	34	GENIC	homozygous	112065371
3	9734308	9734309	T	C	48	GENIC	homozygous	112065373
3	9734504	9734505	A	G	34	GENIC	homozygous	112065375
3	9734627	9734628	A	G	39	GENIC	homozygous	112065377
3	9734874	9734875	G	A	43	GENIC	homozygous	112065379
3	9735071	9735072	A	G	36	GENIC	homozygous	112065381
3	9735339	9735339		AAAC	38	GENIC	homozygous	131325163
3	9735709	9735710	T	A	44	GENIC	homozygous	112065385
3	9735921	9735921		T	14	GENIC	homozygous	131325164
3	9736187	9736188	T	C	42	GENIC	homozygous	112065387
3	9737256	9737257	C	T	46	GENIC	homozygous	112065389
3	9738041	9738042	G	C	46	GENIC	homozygous	112065391
3	9738116	9738117	T	C	34	GENIC	homozygous	112065393
3	9738149	9738150	A	G	36	GENIC	homozygous	112065395
3	9738539	9738540	G	T	56	GENIC	homozygous	112065397