chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	93098138	93098139	A	T	26	GENIC	homozygous	52048252
9	93098914	93098915	G	A	24	GENIC	homozygous	53599543
9	93099101	93099102	G	GA	21	GENIC	homozygous	53179770
9	93099161	93099162	C	A	37	GENIC	homozygous	53599544
9	93099782	93099783	G	GT	24	GENIC	possibly homozygous	53599545
9	93100233	93100234	A	AT	36	GENIC	homozygous	52048262
9	93100375	93100376	A	G	35	GENIC	homozygous	52048263
9	93100682	93100683	A	G	36	GENIC	homozygous	52048265
9	93101001	93101002	T	-	16	GENIC	homozygous	52279137
9	93101104	93101105	G	A	13	GENIC	homozygous	53599546
9	93101400	93101401	C	T	24	GENIC	possibly homozygous	52048273
9	93101751	93101752	T	C	30	GENIC	homozygous	52279138
9	93102094	93102095	C	T	23	GENIC	homozygous	53599547
9	93103518	93103519	T	TTCC	9	GENIC	homozygous	53599548
9	93103555	93103561	TCTTCA	------	22	GENIC	homozygous	52048301
9	93104166	93104168	TC	--	6	GENIC	heterozygous	53599549
9	93104167	93104168	C	-	6	GENIC	heterozygous	52048311
9	93104300	93104301	T	A	29	GENIC	homozygous	53599550
9	93105127	93105128	C	-	29	GENIC	homozygous	52279142
9	93105339	93105340	C	CA	21	GENIC	homozygous	53599551
9	93105927	93105928	G	GCCC	5	GENIC	homozygous	52048325