chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	8501115	8501115		G	12	GENIC	homozygous	131325009
3	8501121	8501122	G	A	13	GENIC	homozygous	111872923
3	8501125	8501126	G	A	12	GENIC	homozygous	111872925
3	8502020	8502021	T	G	22	GENIC	heterozygous	131840100
3	8502044	8502045	T	A	23	GENIC	heterozygous	131840101
3	8502085	8502085		ATCTTT	26	GENIC	heterozygous	127847919
3	8502085	8502086	G	T	26	GENIC	heterozygous	127968171
3	8502116	8502117	G	A	26	GENIC	heterozygous	127968172
3	8502117	8502118	C	G	26	GENIC	heterozygous	127968173
3	8502131	8502132	T	G	28	GENIC	heterozygous	127968174
3	8511936	8511937	G		17	GENIC	homozygous	127847921
3	8511946	8511947	A	G	18	GENIC	homozygous	111872927
3	8511947	8511948	G	A	19	GENIC	homozygous	121735517
3	8511996	8511997	G		18	GENIC	homozygous	127847922
3	8512034	8512034		G	19	GENIC	homozygous	127847923
3	8512053	8512054	C	T	18	GENIC	homozygous	119667011
3	8512054	8512055	T	G	19	GENIC	homozygous	119647575
3	8512085	8512086	A		16	GENIC	homozygous	127847924
3	8512141	8512141		T	15	GENIC	homozygous	127847925
3	8512149	8512150	A		17	GENIC	homozygous	127847926
3	8512152	8512152		A	19	GENIC	homozygous	127847927
3	8517726	8517727	T	C	16	GENIC	homozygous	111441853
3	8519476	8519477	G	A	14	GENIC	homozygous	111441856
3	8520326	8520327	G	A	16	GENIC	homozygous	111872931
3	8521032	8521033	T	A	24	GENIC	possibly homozygous	111872933
3	8521072	8521073	G	A	18	GENIC	homozygous	111872935
3	8521167	8521168	C	T	21	GENIC	homozygous	111441862