chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	53386793	53386794	C	CAGGAGAGAGAGAGAGAGAG	6	GENIC	homozygous	53431154
8	53386904	53386905	A	-	12	GENIC	homozygous	52632591
8	53386910	53386911	G	-	12	GENIC	homozygous	52632593
8	53386914	53386915	G	-	11	GENIC	homozygous	52632595
8	53386921	53386922	G	-	10	GENIC	homozygous	52632597
8	53387021	53387024	TCT	---	2	GENIC	homozygous	53387232
8	53387006	53387007	G	-	6	GENIC	homozygous	53387229
8	53387010	53387012	GA	--	5	GENIC	homozygous	53387230
8	53387017	53387018	C	-	4	GENIC	homozygous	53387231
8	53387050	53387052	GG	--	1	GENIC	homozygous	53387233
8	53387060	53387061	C	-	1	GENIC	homozygous	52632605
8	53387062	53387063	C	-	3	GENIC	homozygous	52632607
8	53387067	53387068	C	-	4	GENIC	homozygous	52632609
8	53387069	53387071	GT	--	4	GENIC	homozygous	52632611
8	53387074	53387075	G	-	4	GENIC	homozygous	52632613
8	53387079	53387080	G	-	4	GENIC	homozygous	52632615
8	53387086	53387087	C	-	5	GENIC	homozygous	52632617
8	53387091	53387092	C	-	7	GENIC	homozygous	52632619
8	53387096	53387097	C	-	10	GENIC	homozygous	52632621
8	53387103	53387104	C	-	11	GENIC	homozygous	52632623
8	53387108	53387109	C	-	13	GENIC	homozygous	52632625
8	53387114	53387115	G	-	14	GENIC	homozygous	52632627
8	53387121	53387122	C	-	15	GENIC	homozygous	52632629
8	53387137	53387138	T	-	18	GENIC	homozygous	52632631
8	53387534	53387535	C	T	31	GENIC	homozygous	52632633
8	53388181	53388186	GCCAC	-----	14	GENIC	homozygous	52976369
8	53389242	53389243	T	-	32	GENIC	homozygous	52976370
8	53389329	53389330	A	ACTCCCAGGGAGCAGGAACTGTATTTTAGTCGCCTGTGCATCTCCATCCCTCAGAAGAGCACTGCCATGTCAGGTAGTCACTGACAGGAGGAGGTGAGAAATGAGAATGGCTTAGTCCTTTCTCTGCTG	43	GENIC	homozygous	53387234
8	53389832	53389833	A	G	16	GENIC	homozygous	52632641
8	53390008	53390009	G	A	19	GENIC	homozygous	52632643
8	53390106	53390107	T	TCATCC	23	GENIC	homozygous	52632645
8	53390449	53390450	A	G	23	GENIC	homozygous	52632647
8	53390491	53390492	C	T	25	GENIC	homozygous	52632649
8	53390914	53390915	C	T	32	GENIC	homozygous	52632651