chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47663710	47663711	C	G	38	GENIC	possibly homozygous	114668863
13	47663845	47663846	T	A	41	GENIC	homozygous	114668865
13	47664086	47664087	C	T	35	GENIC	possibly homozygous	114668866
13	47664260	47664261	G	A	44	GENIC	homozygous	114668868
13	47664421	47664422	G	A	56	GENIC	homozygous	114668870
13	47665099	47665100	T	C	31	GENIC	homozygous	114668872
13	47665421	47665422	A	C	25	GENIC	homozygous	114615089
13	47665553	47665554	C	T	38	GENIC	possibly homozygous	114668874
13	47665613	47665614	G	A	40	GENIC	homozygous	114615090
13	47667185	47667186	G	A	24	GENIC	homozygous	114668880
13	47667468	47667469	A	G	33	GENIC	homozygous	114823603
13	47667672	47667673	G	A	25	GENIC	homozygous	114668882
13	47668016	47668017	T	C	23	GENIC	homozygous	114668884
13	47668098	47668099	T	C	40	GENIC	homozygous	114668886
13	47668118	47668119	A	G	43	GENIC	possibly homozygous	114668888
13	47668275	47668276	A	T	48	GENIC	heterozygous	115218167
13	47668330	47668331	A	T	29	GENIC	heterozygous	118450251
13	47670285	47670286	A	G	23	GENIC	possibly homozygous	114615094
13	47670701	47670702	A	G	11	GENIC	homozygous	115182096
13	47670944	47670945	T	C	33	GENIC	homozygous	114615095
13	47672504	47672505	C	T	40	GENIC	homozygous	114668890
13	47673254	47673255	C	T	28	GENIC	homozygous	114668892
13	47674483	47674484	C	T	41	GENIC	possibly homozygous	114823605
13	47675010	47675011	A	T	42	GENIC	homozygous	114668894
13	47676310	47676311	A	C	38	GENIC	homozygous	114668896
13	47676378	47676379	A	C	31	GENIC	homozygous	114668898
13	47676823	47676824	A	T	45	GENIC	homozygous	114615098
13	47677030	47677031	C	T	46	GENIC	possibly homozygous	114668900
13	47677190	47677191	G	A	36	GENIC	homozygous	114668902
13	47677245	47677246	T	C	36	GENIC	homozygous	114668904
13	47677596	47677597	G	A	42	GENIC	possibly homozygous	114668906
13	47667928	47667929	A	G	18	GENIC	heterozygous	118541635
13	47667938	47667939	A	G	16	GENIC	possibly homozygous	114548339
13	47668183	47668184	A	T	43	GENIC	possibly homozygous	114760320