chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46182802	46182803	A	G	44	GENIC	homozygous	116877594
10	46184578	46184578		T	26	GENIC	possibly homozygous	128814161
10	46184697	46184698	C	T	16	GENIC	homozygous	116585214
10	46185035	46185036	A	G	50	GENIC	homozygous	116585218
10	46185383	46185384	A	G	33	GENIC	homozygous	117410415
10	46185750	46185751	T	C	35	GENIC	homozygous	116585220
10	46185892	46185893	G	A	40	GENIC	homozygous	116877596
10	46186984	46186985	C	A	31	GENIC	homozygous	116877598
10	46187412	46187413	C	A	43	GENIC	homozygous	116585222
10	46188489	46188491	CA		50	GENIC	possibly homozygous	128814163
10	46189626	46189627	A	G	28	GENIC	homozygous	116585224
10	46189693	46189703	TATATGTGTA		27	GENIC	homozygous	131092518
10	46190344	46190345	A	T	27	GENIC	homozygous	116877600
10	46190515	46190516	T	C	49	GENIC	homozygous	116585226
10	46194581	46194582	T	C	47	GENIC	homozygous	116585230
10	46194922	46194923	T	G	57	GENIC	homozygous	116585232
10	46195298	46195299	G	T	43	GENIC	homozygous	116585234
10	46195649	46195651	AC		36	GENIC	possibly homozygous	131092519
10	46196238	46196238		AAAAC	30	GENIC	homozygous	128814166
10	46200048	46200049	A		38	GENIC	homozygous	128814171
10	46200871	46200872	T	G	43	GENIC	homozygous	116877602
10	46201113	46201114	A	G	29	GENIC	homozygous	116585236
10	46201279	46201280	G	A	31	GENIC	homozygous	116877604
10	46202861	46202861		CAGGGCTA	50	GENIC	homozygous	128814172
10	46203017	46203018	A	G	40	GENIC	homozygous	116877606
10	46203732	46203733	T	C	49	GENIC	homozygous	116585238
10	46204813	46204814	T	G	33	GENIC	homozygous	116585240