chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90116679	90116680	A	C	11	GENIC	homozygous	114573695
13	90118924	90118925	C	T	16	GENIC	homozygous	114573697
13	90121548	90121549	T	A	22	GENIC	homozygous	114573699
13	90131561	90131562	G	A	17	GENIC	homozygous	114573703
13	90132375	90132376	A	G	27	GENIC	homozygous	114573705
13	90132424	90132425	C	T	28	GENIC	homozygous	114573707
13	90132444	90132445	C	T	28	GENIC	homozygous	114573709
13	90132482	90132483	G	A	24	GENIC	homozygous	114573711
13	90132895	90132896	T	G	10	GENIC	homozygous	114573713
13	90133061	90133062	A	G	20	GENIC	homozygous	114573715
13	90133190	90133191	G	A	17	GENIC	homozygous	114573717
13	90133221	90133222	G	C	17	GENIC	homozygous	114573719
13	90133725	90133726	C	T	34	GENIC	homozygous	114573721
13	90133831	90133832	A	T	15	GENIC	homozygous	114573723
13	90133946	90133947	C	T	13	GENIC	homozygous	114573725
13	90134155	90134156	T	C	22	GENIC	homozygous	114573727
13	90134269	90134270	C	T	17	GENIC	homozygous	114573729
13	90134274	90134275	A	G	16	GENIC	homozygous	114573731
13	90134689	90134690	C	T	13	GENIC	homozygous	114573733
13	90135256	90135257	G	A	12	GENIC	homozygous	114573735
13	90135325	90135326	T	C	11	GENIC	homozygous	114573737
13	90135696	90135697	T	C	20	GENIC	homozygous	114573739
13	90135855	90135856	T	C	16	GENIC	homozygous	114573741
13	90135880	90135881	G	A	16	GENIC	homozygous	114573743
13	90135888	90135889	C	T	19	GENIC	homozygous	114573745
13	90135894	90135895	G	A	18	GENIC	homozygous	114573747
13	90136076	90136077	G	A	19	GENIC	homozygous	114573749
13	90136367	90136368	C	A	17	GENIC	homozygous	114573751
13	90136381	90136382	A	G	17	GENIC	homozygous	114573753
13	90136827	90136828	C	T	25	GENIC	homozygous	114573755
13	90136884	90136885	G	A	25	GENIC	homozygous	114573757
13	90137867	90137868	A	T	15	GENIC	homozygous	114573759
13	90138119	90138120	G	T	18	GENIC	homozygous	114573761
13	90138120	90138121	C	T	18	GENIC	homozygous	114573763
13	90139259	90139260	G	C	27	GENIC	homozygous	114573765