chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	40612106	40612107	T	-	19	GENIC	homozygous	49731466
13	40612116	40612117	C	-	17	GENIC	homozygous	49731467
13	40613319	40613320	T	C	18	GENIC	homozygous	49731470
13	40614655	40614656	C	-	11	GENIC	homozygous	49731475
13	40614828	40614829	C	-	8	GENIC	homozygous	49731476
13	40614856	40614857	G	GT	8	GENIC	homozygous	49731477
13	40616163	40616164	G	T	16	GENIC	homozygous	49731481
13	40616202	40616203	A	G	14	GENIC	homozygous	49731482
13	40617037	40617038	G	A	10	GENIC	homozygous	49731484
13	40617092	40617093	T	C	8	GENIC	homozygous	49731485
13	40617782	40617783	C	T	10	GENIC	homozygous	49731487
13	40617866	40617867	T	G	8	GENIC	homozygous	49731488
13	40617948	40617949	G	A	10	GENIC	homozygous	49731489
13	40618382	40618383	C	G	9	GENIC	homozygous	49731490
13	40618437	40618438	C	A	11	GENIC	homozygous	49731491
13	40618734	40618735	G	A	7	GENIC	homozygous	49731492
13	40619064	40619065	T	C	8	GENIC	homozygous	49731493
13	40619607	40619608	G	A	11	GENIC	homozygous	50492512
13	40619742	40619743	T	G	15	GENIC	homozygous	49731494
13	40619775	40619776	T	C	13	GENIC	homozygous	49731495
13	40623183	40623184	G	T	7	GENIC	homozygous	49731509
13	40623695	40623696	T	C	14	GENIC	homozygous	49731510
13	40623696	40623697	C	CAG	14	GENIC	homozygous	49731511
13	40623697	40623698	T	C	14	GENIC	homozygous	50492514
13	40623860	40623861	C	T	12	GENIC	homozygous	49731512
13	40624260	40624261	A	T	14	GENIC	homozygous	50492515
13	40625196	40625197	G	T	9	GENIC	homozygous	49731513
13	40625726	40625727	T	C	15	GENIC	homozygous	49731516
13	40628283	40628284	T	-	8	GENIC	homozygous	49731519
13	40630212	40630213	T	G	12	GENIC	homozygous	49731520
13	40631247	40631248	A	G	16	GENIC	homozygous	49731521
13	40633017	40633018	A	C	14	GENIC	homozygous	49731526
13	40634649	40634650	G	A	7	GENIC	homozygous	50492517
13	40636528	40636529	T	C	12	GENIC	homozygous	50492519
13	40641122	40641123	C	T	15	GENIC	homozygous	49731549
13	40646128	40646129	C	G	7	GENIC	homozygous	51273924