chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	47893518	47893519	C	A	13	GENIC	homozygous	52621321
8	47893918	47893919	C	CTTCCTTCT	13	GENIC	homozygous	53429569
8	47894033	47894034	T	G	11	GENIC	homozygous	52621327
8	47894296	47894297	C	CAGATAGATAGATAGAT	2	GENIC	homozygous	53429571
8	47894347	47894348	A	G	22	GENIC	homozygous	52621334
8	47894568	47894573	AAAAG	-----	15	GENIC	homozygous	52621338
8	47894781	47894782	A	AAGGACATTCTTTTTTTTTTTTTTTTTTGGGTTCTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC	18	GENIC	heterozygous	53429573
8	47895112	47895113	C	A	14	GENIC	homozygous	52621342
8	47896183	47896184	T	A	21	GENIC	homozygous	52621344
8	47896369	47896370	C	CTCCTTCCTTCCT	14	GENIC	homozygous	53429575
8	47896399	47896402	TTC	---	6	GENIC	homozygous	53799744
8	47896408	47896409	C	-	8	GENIC	possibly homozygous	53799746
8	47896507	47896508	G	T	23	GENIC	homozygous	52621362
8	47896939	47896949	TTGTGTGTGT	----------	1	GENIC	homozygous	53429581
8	47896978	47896984	TGTGTA	------	5	GENIC	heterozygous	53603900
8	47897268	47897269	G	C	11	GENIC	homozygous	52621364
8	47897432	47897433	A	G	9	GENIC	homozygous	52621366
8	47897586	47897587	C	CTTCCTCCCTCCT	1	GENIC	homozygous	53506777
8	47897614	47897615	C	CT	6	GENIC	homozygous	52621374
8	47897679	47897680	T	C	14	GENIC	homozygous	52621376
8	47897711	47897712	C	CTCTTTCTTTCTT	2	GENIC	heterozygous	53382260
8	47897711	47897712	C	CTCTTTCTTTCTTTCTT	2	GENIC	heterozygous	53429583
8	47897775	47897776	C	CTTCCTTCT	7	GENIC	homozygous	53363470
8	47898166	47898170	GTGT	----	7	GENIC	heterozygous	53429585
8	47898168	47898170	GT	--	7	GENIC	heterozygous	53429587
8	47898178	47898182	TGTG	----	4	GENIC	heterozygous	53429591
8	47898709	47898710	C	T	5	GENIC	homozygous	52621382
8	47898730	47898731	C	T	7	GENIC	homozygous	52621384
8	47898794	47898795	G	A	1	GENIC	homozygous	52621386