chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	15099983	15099984	A	G	42	GENIC	heterozygous	116497709
10	15099997	15099998	C	T	41	GENIC	heterozygous	116497711
10	15100001	15100002	C	T	44	GENIC	heterozygous	116497713
10	15100064	15100065	G	A	44	GENIC	heterozygous	116497715
10	15100306	15100307	C	T	52	GENIC	heterozygous	116737568
10	15100368	15100369	G	A	34	GENIC	heterozygous	116497717
10	15100376	15100377	T	C	33	GENIC	heterozygous	116497719
10	15100528	15100529	C	T	36	GENIC	heterozygous	117074910
10	15101021	15101022	C	T	19	GENIC	homozygous	116737569
10	15101960	15101961	C	T	38	GENIC	heterozygous	117074911
10	15101972	15101973	T	C	34	GENIC	heterozygous	116497725
10	15102102	15102103	C	T	53	GENIC	heterozygous	116497735
10	15102120	15102121	C	A	46	GENIC	heterozygous	116497737
10	15102144	15102145	A	G	39	GENIC	heterozygous	116497739
10	15102149	15102150	C	T	38	GENIC	heterozygous	116497741
10	15102150	15102151	A	G	35	GENIC	heterozygous	116497743
10	15102162	15102163	C	T	32	GENIC	heterozygous	116497745
10	15102212	15102213	A	G	50	GENIC	heterozygous	116497747
10	15102251	15102252	A	G	50	GENIC	heterozygous	116497749
10	15102273	15102274	A	G	38	GENIC	heterozygous	116497751
10	15102301	15102302	A	G	25	GENIC	heterozygous	116497753
10	15102513	15102514	T	C	46	GENIC	heterozygous	116859931
10	15102531	15102532	C	T	39	GENIC	heterozygous	116859933