chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	88394208	88394209	G	A	26	GENIC	homozygous	51729697
10	88394810	88394811	G	C	38	GENIC	homozygous	51729699
10	88395774	88395775	G	GGTGT	11	GENIC	heterozygous	51535181
10	88396918	88396919	G	A	30	GENIC	homozygous	51729701
10	88397927	88397928	G	A	33	GENIC	homozygous	51729703
10	88398439	88398440	T	A	21	GENIC	homozygous	51729705
10	88398983	88398984	A	C	19	GENIC	homozygous	51729707
10	88399131	88399132	C	T	17	GENIC	heterozygous	51729709
10	88399427	88399428	C	T	3	GENIC	homozygous	51729711
10	88399434	88399435	T	TA	1	GENIC	homozygous	51729713
10	88399989	88399990	A	G	22	GENIC	possibly homozygous	51729715
10	88400026	88400027	C	A	15	GENIC	homozygous	51535184
10	88400253	88400254	T	C	27	GENIC	homozygous	51729719
10	88400469	88400470	A	G	27	GENIC	homozygous	51729721
10	88400482	88400483	G	T	25	GENIC	homozygous	51729723
10	88400875	88400876	G	A	26	GENIC	homozygous	51729729
10	88400961	88400962	T	-	16	GENIC	possibly homozygous	51729731
10	88401645	88401646	G	A	27	GENIC	homozygous	51729733
10	88401782	88401783	G	A	28	GENIC	homozygous	51729734