chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	44579585	44579586	C	T	53	GENIC	homozygous	114781157
6	44580106	44580107	C	T	43	GENIC	homozygous	114781159
6	44580313	44580314	A	C	42	GENIC	homozygous	114781161
6	44580361	44580362	T	G	40	GENIC	homozygous	114781163
6	44580638	44580639	A	G	63	GENIC	homozygous	114781165
6	44580900	44580901	T	C	31	GENIC	possibly homozygous	114781167
6	44581306	44581307	A	T	33	GENIC	homozygous	114781173
6	44581482	44581483	A	G	35	GENIC	homozygous	114781175
6	44583566	44583567	A	G	40	GENIC	homozygous	114781177
6	44584380	44584381	T	C	31	GENIC	homozygous	114781181
6	44584592	44584593	A	C	35	GENIC	homozygous	114781183
6	44584690	44584691	A	C	49	GENIC	homozygous	114781185
6	44585105	44585106	G	C	45	GENIC	homozygous	114781189
6	44585754	44585755	C	T	43	GENIC	homozygous	114781191
6	44585799	44585800	A	G	34	GENIC	homozygous	114781193
6	44586956	44586957	T	A	37	GENIC	homozygous	114781195
6	44587001	44587002	A	C	25	GENIC	homozygous	114781197
6	44587029	44587030	C	T	26	GENIC	homozygous	114781199
6	44587033	44587034	T	C	29	GENIC	homozygous	114781201
6	44588139	44588140	G	A	46	GENIC	homozygous	114781205