chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	13447314	13447315	C	G	18	GENIC	homozygous	114725911
6	13448900	13448901	A	G	24	GENIC	possibly homozygous	114725913
6	13450366	13450367	C	T	26	GENIC	possibly homozygous	114725915
6	13450640	13450641	T	G	35	GENIC	possibly homozygous	114725917
6	13451582	13451583	T	C	31	GENIC	homozygous	114725919
6	13452152	13452153	T	C	24	GENIC	possibly homozygous	114725921
6	13454638	13454639	T	A	24	GENIC	homozygous	114725927
6	13454763	13454764	G	C	10	GENIC	homozygous	114725941
6	13454899	13454900	A	C	24	GENIC	possibly homozygous	114725943
6	13455447	13455448	G	A	20	GENIC	possibly homozygous	114725947
6	13455461	13455462	T	C	20	GENIC	possibly homozygous	114725949
6	13455734	13455735	T	C	20	GENIC	possibly homozygous	114725951
6	13456644	13456645	T	A	25	GENIC	homozygous	114725953
6	13456645	13456646	T	A	25	GENIC	homozygous	114725955
6	13458247	13458248	T	C	29	GENIC	homozygous	114725957
6	13459078	13459079	C	T	14	GENIC	homozygous	114725965
6	13459199	13459200	T	C	22	GENIC	homozygous	114725967
6	13459273	13459274	C	T	23	GENIC	homozygous	114725969
6	13460557	13460558	G	T	23	GENIC	homozygous	114725973
6	13462367	13462368	G	A	22	GENIC	possibly homozygous	114725975
6	13462433	13462434	C	G	28	GENIC	possibly homozygous	114725977