chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	123734573	123734574	G	A	37	GENIC	homozygous	138441220
8	123735037	123735038	G	A	39	GENIC	homozygous	142107903
8	123735050	123735051	T	A	38	GENIC	homozygous	142107904
8	123735391	123735392	A	G	48	GENIC	homozygous	142107905
8	123735698	123735699	T	G	51	GENIC	homozygous	142107906
8	123736562	123736563	G	T	43	GENIC	homozygous	138441222
8	123736612	123736613	C	T	47	GENIC	homozygous	138441223
8	123737067	123737068	C	T	51	GENIC	homozygous	142107907
8	123737411	123737412	G	A	39	GENIC	homozygous	138441226
8	123737501	123737502	C	A	42	GENIC	homozygous	142107908
8	123737751	123737752	A	G	40	GENIC	homozygous	142107909
8	123738850	123738851	C	T	44	GENIC	homozygous	142107910
8	123739556	123739557	T	C	29	GENIC	homozygous	142107911
8	123739687	123739688	C	T	38	GENIC	homozygous	142107912
8	123740089	123740090	G	A	40	GENIC	homozygous	138441229
8	123740276	123740277	C	T	47	GENIC	homozygous	142107913
8	123735269	123735270	C	T	6	GENIC	heterozygous	404416226
8	123735269	123735270	C		6	GENIC	heterozygous	404416227
8	123736134	123736134		GGAATGT	43	GENIC	homozygous	142032351
8	123740958	123740958		T	38	GENIC	homozygous	142032352