chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46184057	46184058	C	A	21	GENIC	homozygous	116585212
10	46184578	46184578		T	9	GENIC	homozygous	128814161
10	46184697	46184698	C	T	10	GENIC	homozygous	116585214
10	46185002	46185003	C	T	18	GENIC	homozygous	116585216
10	46185035	46185036	A	G	16	GENIC	homozygous	116585218
10	46185383	46185384	A	G	16	GENIC	homozygous	117410415
10	46185750	46185751	T	C	34	GENIC	homozygous	116585220
10	46187412	46187413	C	A	17	GENIC	homozygous	116585222
10	46188489	46188491	CA		14	GENIC	homozygous	128814163
10	46189608	46189609	A	G	26	GENIC	homozygous	123441210
10	46189614	46189615	A	G	25	GENIC	homozygous	123441211
10	46189620	46189621	A	G	24	GENIC	homozygous	123441212
10	46189626	46189627	A	G	25	GENIC	homozygous	116585224
10	46189631	46189633	TA		24	GENIC	homozygous	128814164
10	46189713	46189721	TATATGTG		29	GENIC	homozygous	128814165
10	46190515	46190516	T	C	28	GENIC	homozygous	116585226
10	46192416	46192417	T	G	27	GENIC	homozygous	116585228
10	46194581	46194582	T	C	14	GENIC	homozygous	116585230
10	46196610	46196630	TGTGTGTGTGTATCTGTGTG		28	GENIC	homozygous	128814169
10	46185980	46185981	C	T	19	GENIC	homozygous	117129048
10	46189624	46189625	A	G	25	GENIC	homozygous	128869083
10	46196238	46196238		AAAAC	17	GENIC	homozygous	128814166
10	46196523	46196523		T	21	GENIC	possibly homozygous	128814167
10	46196578	46196582	TGTG		23	GENIC	homozygous	128814168
10	46194922	46194923	T	G	15	GENIC	homozygous	116585232
10	46195298	46195299	G	T	17	GENIC	homozygous	116585234
10	46197511	46197513	AG		16	GENIC	homozygous	128814170
10	46198081	46198082	G	C	25	GENIC	homozygous	116931244
10	46200048	46200049	A		19	GENIC	homozygous	128814171
10	46201113	46201114	A	G	20	GENIC	homozygous	116585236
10	46202861	46202861		CAGGGCTA	23	GENIC	homozygous	128814172
10	46203732	46203733	T	C	16	GENIC	homozygous	116585238
10	46204813	46204814	T	G	15	GENIC	homozygous	116585240
10	46205165	46205166	C	A	10	GENIC	homozygous	117993467
10	46205168	46205168		C	10	GENIC	homozygous	128814173