chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	77615979	77615980	A	G	39	GENIC	homozygous	136756035
3	77616001	77616002	G	C	44	GENIC	homozygous	136756036
3	77616346	77616347	A	G	42	GENIC	homozygous	136756037
3	77616397	77616398	T	C	52	GENIC	homozygous	136756038
3	77616767	77616768	C	T	66	GENIC	homozygous	136756039
3	77617185	77617186	C	T	50	GENIC	homozygous	136756040
3	77617407	77617408	G	T	66	GENIC	possibly homozygous	136756041
3	77617599	77617600	C	T	43	GENIC	homozygous	143905708
3	77617639	77617640	G	A	51	GENIC	homozygous	136756043
3	77617957	77617957		GCTGGGT	42	GENIC	homozygous	136574387
3	77618133	77618134	T	C	51	GENIC	homozygous	136756044
3	77618454	77618455	A		57	GENIC	homozygous	136574388
3	77618754	77618755	T	C	50	GENIC	homozygous	136756045
3	77619034	77619035	C	T	43	GENIC	homozygous	143905709
3	77619058	77619059	C	A	46	GENIC	homozygous	136756046
3	77619655	77619656	C	T	41	GENIC	homozygous	136756047
3	77620019	77620020	T	C	47	GENIC	homozygous	136756048
3	77620705	77620706	C	T	56	GENIC	homozygous	136756049
3	77620736	77620736		C	56	GENIC	homozygous	136574389
3	77620794	77620795	T	C	72	GENIC	homozygous	136756050
3	77620817	77620818	C	T	64	GENIC	homozygous	136756051
3	77621118	77621119	G	A	58	GENIC	possibly homozygous	136756052
3	77621285	77621286	T	G	38	GENIC	homozygous	136756053
3	77621283	77621284	T		38	GENIC	homozygous	403069111
3	77621283	77621284	T	G	38	GENIC	heterozygous	403069112