chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	77615979	77615980	A	G	43	GENIC	homozygous	136756035
3	77616001	77616002	G	C	38	GENIC	homozygous	136756036
3	77616346	77616347	A	G	60	GENIC	homozygous	136756037
3	77616397	77616398	T	C	56	GENIC	homozygous	136756038
3	77616767	77616768	C	T	61	GENIC	homozygous	136756039
3	77617185	77617186	C	T	65	GENIC	homozygous	136756040
3	77617407	77617408	G	T	74	GENIC	homozygous	136756041
3	77617584	77617585	C	T	70	GENIC	homozygous	146389601
3	77617639	77617640	G	A	57	GENIC	homozygous	136756043
3	77618133	77618134	T	C	72	GENIC	homozygous	136756044
3	77618754	77618755	T	C	48	GENIC	homozygous	136756045
3	77619058	77619059	C	A	57	GENIC	homozygous	136756046
3	77619655	77619656	C	T	35	GENIC	homozygous	136756047
3	77620019	77620020	T	C	53	GENIC	homozygous	136756048
3	77620705	77620706	C	T	60	GENIC	homozygous	136756049
3	77620794	77620795	T	C	51	GENIC	homozygous	136756050
3	77620817	77620818	C	T	49	GENIC	homozygous	136756051
3	77621118	77621119	G	A	54	GENIC	homozygous	136756052
3	77620736	77620736		C	58	GENIC	homozygous	136574389
3	77621289	77621295	TTTTTG		30	GENIC	homozygous	146370914
3	77617957	77617957		GCTGGGT	74	GENIC	homozygous	136574387
3	77618454	77618455	A		45	GENIC	homozygous	136574388
3	77621283	77621284	T	G	35	GENIC	homozygous	403069112
3	77621283	77621284	T		35	GENIC	heterozygous	403069111