chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	6661553	6661554	A	G	37	GENIC	homozygous	111927130
16	6662171	6662172	G	A	19	GENIC	homozygous	111927132
16	6662823	6662824	C	T	34	GENIC	homozygous	111711366
16	6663518	6663519	G	A	46	GENIC	possibly homozygous	111927134
16	6663653	6663654	C	A	37	GENIC	homozygous	111927136
16	6664734	6664735	A	G	37	GENIC	homozygous	111927138
16	6665405	6665406	G	A	41	GENIC	homozygous	111927140
16	6665642	6665643	T	C	49	GENIC	homozygous	111927142
16	6665743	6665744	T	C	43	GENIC	homozygous	111711368
16	6666639	6666640	A	G	33	GENIC	homozygous	111711370
16	6667474	6667475	T	C	48	GENIC	homozygous	111927144
16	6672093	6672094	T	C	44	GENIC	homozygous	111711378
16	6673235	6673236	C	T	26	GENIC	homozygous	111711380
16	6674289	6674290	G	A	39	GENIC	homozygous	111711384
16	6674507	6674508	C	A	26	GENIC	possibly homozygous	119093822
16	6674684	6674685	G	T	5	GENIC	homozygous	119141559
16	6674714	6674715	T	G	3	GENIC	homozygous	119141561
16	6675169	6675170	T	G	28	GENIC	homozygous	119093825
16	6675321	6675322	A	G	54	GENIC	possibly homozygous	111711386
16	6675388	6675389	C	T	64	GENIC	homozygous	112144741
16	6675447	6675448	A	G	44	GENIC	homozygous	111711388
16	6675677	6675678	T	C	26	GENIC	homozygous	111711390