chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52645521	52645522	C	T	17	GENIC	homozygous	114550660
13	52645671	52645672	G	A	25	GENIC	homozygous	114550661
13	52646810	52646811	A	G	14	GENIC	homozygous	114550662
13	52647112	52647113	T	C	22	GENIC	homozygous	114550663
13	52647221	52647222	A	C	24	GENIC	homozygous	114550664
13	52647698	52647699	T	A	23	GENIC	homozygous	114550665
13	52648134	52648135	T	C	36	GENIC	homozygous	114550666
13	52648369	52648370	T	A	30	GENIC	homozygous	114550667
13	52650080	52650081	C	T	26	GENIC	homozygous	114550669
13	52650712	52650713	A	G	39	GENIC	homozygous	114550670
13	52650714	52650715	A	G	37	GENIC	homozygous	114550671
13	52651007	52651008	C	T	22	GENIC	homozygous	114550672
13	52651074	52651075	C	T	29	GENIC	homozygous	114550673
13	52651244	52651245	T	A	25	GENIC	homozygous	114550674
13	52651437	52651438	G	A	40	GENIC	homozygous	114550675
13	52651572	52651573	A	G	38	GENIC	homozygous	114550676
13	52652622	52652623	G	T	43	GENIC	homozygous	114550677
13	52653603	52653604	T	A	10	GENIC	homozygous	114550682
13	52653662	52653663	G	A	13	GENIC	homozygous	114550683
13	52654921	52654922	G	T	16	GENIC	homozygous	114550684
13	52655088	52655089	G	A	42	GENIC	homozygous	114550685
13	52656170	52656171	C	A	28	GENIC	homozygous	114550686
13	52656528	52656529	T	C	26	GENIC	homozygous	114550687