chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46182802	46182803	A	G	11	GENIC	homozygous	116877594
10	46185750	46185751	T	C	14	GENIC	homozygous	116585220
10	46183733	46183734	T	C	9	GENIC	homozygous	117218260
10	46184697	46184698	C	T	18	GENIC	homozygous	116585214
10	46185035	46185036	A	G	33	GENIC	possibly homozygous	116585218
10	46185892	46185893	G	A	17	GENIC	homozygous	116877596
10	46186984	46186985	C	A	18	GENIC	homozygous	116877598
10	46187412	46187413	C	A	11	GENIC	homozygous	116585222
10	46190344	46190345	A	T	32	GENIC	homozygous	116877600
10	46190515	46190516	T	C	29	GENIC	homozygous	116585226
10	46194581	46194582	T	C	9	GENIC	homozygous	116585230
10	46194922	46194923	T	G	23	GENIC	homozygous	116585232
10	46195298	46195299	G	T	19	GENIC	homozygous	116585234
10	46200871	46200872	T	G	18	GENIC	homozygous	116877602
10	46201113	46201114	A	G	20	GENIC	homozygous	116585236
10	46201279	46201280	G	A	23	GENIC	homozygous	116877604
10	46203017	46203018	A	G	23	GENIC	homozygous	116877606
10	46203732	46203733	T	C	21	GENIC	homozygous	116585238
10	46204813	46204814	T	G	20	GENIC	homozygous	116585240