chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46183100	46183101	C	T	27	GENIC	homozygous	116772328
10	46184697	46184698	C	T	20	GENIC	homozygous	116585214
10	46185144	46185145	G	A	29	GENIC	homozygous	116772330
10	46185750	46185751	T	C	33	GENIC	homozygous	116585220
10	46187412	46187413	C	A	32	GENIC	homozygous	116585222
10	46190515	46190516	T	C	26	GENIC	homozygous	116585226
10	46191396	46191397	C	T	38	GENIC	homozygous	116772332
10	46194581	46194582	T	C	31	GENIC	homozygous	116585230
10	46194922	46194923	T	G	26	GENIC	homozygous	116585232
10	46195117	46195118	A	G	38	GENIC	homozygous	116772334
10	46195298	46195299	G	T	27	GENIC	homozygous	116585234
10	46197537	46197538	G	A	34	GENIC	homozygous	116772336
10	46198312	46198313	T	A	31	GENIC	homozygous	116772338
10	46199330	46199331	A	G	31	GENIC	possibly homozygous	116772340
10	46200282	46200283	T	G	34	GENIC	homozygous	116772342
10	46201113	46201114	A	G	35	GENIC	homozygous	116585236
10	46202668	46202669	G	A	52	GENIC	homozygous	116772344
10	46203732	46203733	T	C	29	GENIC	homozygous	116585238
10	46204813	46204814	T	G	48	GENIC	homozygous	116585240