chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	22981079	22981080	A	C	52	GENIC	homozygous	116439652
8	22981862	22981863	C	T	48	GENIC	homozygous	116439653
8	22985283	22985284	C	T	47	GENIC	homozygous	116439656
8	22985873	22985874	G	A	35	GENIC	homozygous	116439657
8	22986555	22986556	A	G	43	GENIC	homozygous	116439658
8	22986822	22986823	T	A	54	GENIC	homozygous	116439659
8	22989142	22989143	G	A	43	GENIC	homozygous	116439660
8	22989176	22989177	G	A	45	GENIC	homozygous	116439661
8	22989292	22989293	C	T	55	GENIC	homozygous	116439662
8	22989361	22989362	T	G	55	GENIC	homozygous	116439663
8	22989414	22989415	C	T	48	GENIC	homozygous	116439664
8	22989521	22989522	A	C	44	GENIC	homozygous	116439665
8	22993181	22993182	T	C	33	GENIC	homozygous	116439666
8	22995438	22995439	A	T	18	GENIC	homozygous	116439667
8	22995665	22995666	T	C	17	GENIC	homozygous	116439669
8	22997758	22997759	A	G	38	GENIC	possibly homozygous	116439670
8	22998187	22998188	T	C	35	GENIC	homozygous	116439671
8	22998248	22998249	G	A	31	GENIC	homozygous	116439672
8	22995548	22995549	T	C	3	GENIC	heterozygous	128654261
8	22985173	22985173		A	32	GENIC	possibly homozygous	128574925
8	22985217	22985217		T	43	GENIC	homozygous	128574926
8	22995216	22995216		GA	26	GENIC	homozygous	128574927
8	22995582	22995582		CTTCCTTC	5	GENIC	homozygous	128574928
8	22991987	22991988	T	A	39	GENIC	homozygous	116779171
8	22991988	22991989	T	A	39	GENIC	homozygous	116779173