chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	76677048	76677049	C	T	59	GENIC	homozygous	114863304
6	76679957	76679958	A	G	47	GENIC	homozygous	114863306
6	76683961	76683962	C	T	56	GENIC	homozygous	114863311
6	76684009	76684010	A	G	52	GENIC	homozygous	114863312
6	76684289	76684290	C	T	55	GENIC	homozygous	114863313
6	76686566	76686567	A	G	42	GENIC	homozygous	114863314
6	76686858	76686859	T	C	49	GENIC	homozygous	114863315
6	76679659	76679660	C	T	47	GENIC	homozygous	115258842
6	76683046	76683046		T	47	GENIC	possibly homozygous	128355879
6	76683395	76683395		T	64	GENIC	homozygous	128355880
6	76687932	76687932		TCC	45	GENIC	possibly homozygous	128355882
6	76690015	76690016	A	G	47	GENIC	homozygous	114863316
6	76690278	76690279	A	G	47	GENIC	homozygous	114863317
6	76691697	76691698	T	G	47	GENIC	possibly homozygous	114863318
6	76692552	76692553	A		34	GENIC	homozygous	128355884
6	76693386	76693386		GTCT	47	GENIC	homozygous	128355885
6	76693727	76693728	C	A	49	GENIC	homozygous	114863319
6	76694405	76694406	G	C	38	GENIC	homozygous	114863320
6	76694901	76694902	A	G	48	GENIC	homozygous	114863322
6	76695513	76695514	T	G	22	GENIC	homozygous	115258844
6	76699302	76699303	C	T	3	GENIC	homozygous	126353632