chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	88382148	88382149	G	-	2	GENIC	homozygous	62688490
1	88382215	88382216	A	G	12	GENIC	homozygous	61458559
1	88382836	88382837	C	T	22	GENIC	possibly homozygous	62688491
1	88385256	88385260	GGTC	----	11	GENIC	homozygous	62622096
1	88385955	88385956	G	A	37	GENIC	possibly homozygous	62688492
1	88386691	88386692	A	G	27	GENIC	homozygous	61458566
1	88388204	88388205	C	T	25	GENIC	homozygous	62622098
1	88388573	88388574	A	G	36	GENIC	homozygous	61458567
1	88389660	88389661	T	C	39	GENIC	possibly homozygous	61458569
1	88390104	88390105	C	T	29	GENIC	homozygous	62688493
1	88390921	88390922	G	GGCACA	11	GENIC	possibly homozygous	62263004
1	88392009	88392010	C	T	29	GENIC	possibly homozygous	62688494
1	88393125	88393126	A	T	11	GENIC	possibly homozygous	62688495
1	88393139	88393140	C	CA	13	GENIC	heterozygous	62688496
1	88393142	88393143	C	A	13	GENIC	possibly homozygous	62015556
1	88393145	88393146	C	A	24	GENIC	possibly homozygous	61458573
1	88394410	88394411	T	-	7	GENIC	heterozygous	62688497
1	88394412	88394417	TGTGT	-----	6	GENIC	heterozygous	62688498
1	88394528	88394529	A	AG	25	GENIC	possibly homozygous	61458575
1	88395472	88395473	T	A	27	GENIC	possibly homozygous	62688499
1	88396181	88396182	A	C	26	GENIC	possibly homozygous	62622102
1	88397853	88397854	C	T	30	GENIC	possibly homozygous	62622103
1	88398927	88398928	C	CTT	3	GENIC	homozygous	61458578
1	88399232	88399233	T	C	20	GENIC	possibly homozygous	61458579
1	88400561	88400562	C	T	34	GENIC	homozygous	61458584
1	88401733	88401734	G	A	35	GENIC	homozygous	62688500
1	88402237	88402238	C	CA	11	GENIC	homozygous	60758387
1	88391165	88391167	TA	--	10	GENIC	possibly homozygous	62349991
1	88391840	88391841	T	TGAGAGAGAGAGA	19	GENIC	possibly homozygous	62228260