chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	14303979	14303980	C	T	25	GENIC	homozygous	51762438
9	14303996	14303997	C	-	24	GENIC	homozygous	51762440
9	14304091	14304092	A	G	21	GENIC	homozygous	51762442
9	14304649	14304650	G	A	19	GENIC	homozygous	51762444
9	14305183	14305184	T	C	17	GENIC	homozygous	51762446
9	14305241	14305242	T	-	25	GENIC	homozygous	51762448
9	14305380	14305381	C	G	14	GENIC	homozygous	51762450
9	14305846	14305847	G	-	20	GENIC	homozygous	51762452
9	14305924	14305925	A	G	26	GENIC	homozygous	51762454
9	14306515	14306521	TTTTTT	------	10	GENIC	homozygous	51762456
9	14306802	14306803	C	T	12	GENIC	homozygous	51762458
9	14306886	14306887	A	G	19	GENIC	homozygous	51762460
9	14306893	14306894	T	C	16	GENIC	homozygous	51762462
9	14307720	14307721	G	A	28	GENIC	homozygous	51762464
9	14308042	14308043	G	A	7	GENIC	homozygous	51762468
9	14308099	14308100	A	-	10	GENIC	homozygous	51762470
9	14308240	14308241	T	G	15	GENIC	homozygous	51762472
9	14308260	14308261	C	T	11	GENIC	homozygous	51762474
9	14308476	14308477	C	A	25	GENIC	possibly homozygous	51762476
9	14308501	14308502	T	C	30	GENIC	homozygous	51762478
9	14308993	14308994	C	T	19	GENIC	homozygous	51762480
9	14309142	14309143	G	GACGA	14	GENIC	homozygous	51762482
9	14309588	14309589	T	C	20	GENIC	homozygous	51762484
9	14311566	14311567	A	G	17	GENIC	homozygous	51762486
9	14311967	14311968	T	C	13	GENIC	homozygous	51762488
9	14312381	14312382	C	T	18	GENIC	homozygous	51762490
9	14312584	14312586	GA	--	5	GENIC	heterozygous	52898681
9	14312807	14312808	T	C	23	GENIC	homozygous	51762494
9	14313634	14313635	C	CT	10	GENIC	possibly homozygous	52898683
9	14314212	14314213	G	-	13	GENIC	homozygous	51762496
9	14314331	14314332	A	ATGCT	9	GENIC	homozygous	52843417
9	14314335	14314340	CCCCC	-----	11	GENIC	homozygous	52843420
9	14314551	14314552	A	T	25	GENIC	homozygous	51762498