chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	111828905	111828906	C	T	56	GENIC	homozygous	114447927
13	111830177	111830178	C	T	74	GENIC	possibly homozygous	114447929
13	111831008	111831009	G	A	54	GENIC	homozygous	114447931
13	111831205	111831206	C	A	57	GENIC	possibly homozygous	114447933
13	111831233	111831234	T	G	57	GENIC	homozygous	114447935
13	111831444	111831445	C	A	54	GENIC	homozygous	114447937
13	111831982	111831983	C	T	48	GENIC	possibly homozygous	114447939
13	111832046	111832047	A	G	52	GENIC	possibly homozygous	114447941
13	111834454	111834455	A	G	44	GENIC	possibly homozygous	114447943
13	111837301	111837302	G	T	54	GENIC	homozygous	114447945
13	111837526	111837527	T	C	69	GENIC	homozygous	114447947
13	111839288	111839289	A	C	54	GENIC	homozygous	114447949
13	111840228	111840229	T	C	66	GENIC	homozygous	114447951
13	111841232	111841233	A	G	58	GENIC	possibly homozygous	114447953
13	111841276	111841277	T	C	54	GENIC	possibly homozygous	114447955
13	111842123	111842124	T	A	64	GENIC	homozygous	114447957
13	111843735	111843736	T	C	46	GENIC	homozygous	114447959
13	111843988	111843989	A	T	66	GENIC	homozygous	114447961
13	111844335	111844336	A	G	59	GENIC	homozygous	114447963
13	111844357	111844358	G	A	49	GENIC	homozygous	114447965
13	111844359	111844360	T	C	50	GENIC	homozygous	114447967
13	111844429	111844430	C	T	61	GENIC	possibly homozygous	114447969
13	111844518	111844519	A	C	58	GENIC	possibly homozygous	114447971
13	111844581	111844582	T	C	62	GENIC	homozygous	114447973
13	111844635	111844636	A	G	73	GENIC	homozygous	114447975
13	111844674	111844675	A	G	61	GENIC	homozygous	114447977
13	111844706	111844707	T	C	53	GENIC	homozygous	114447979
13	111847156	111847157	C	G	64	GENIC	possibly homozygous	114447981
13	111847379	111847380	A	G	52	GENIC	homozygous	114447983