chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	113692725	113692726	C	G	24	GENIC	homozygous	114841049
13	113694240	113694241	A	G	18	GENIC	homozygous	114453339
13	113695554	113695555	A	G	16	GENIC	homozygous	114453343
13	113695640	113695641	T	C	13	GENIC	homozygous	114453345
13	113695977	113695978	A	G	21	GENIC	homozygous	114453349
13	113696189	113696190	G	A	17	GENIC	homozygous	114841053
13	113696213	113696214	G	A	14	GENIC	homozygous	114841055
13	113696218	113696219	T	C	12	GENIC	homozygous	114453351
13	113698165	113698166	T	A	19	GENIC	homozygous	115197965
13	113699138	113699139	A	G	15	GENIC	homozygous	114841057
13	113699490	113699491	T	C	14	GENIC	homozygous	114841059
13	113699616	113699617	C	G	20	GENIC	homozygous	114453355
13	113699974	113699975	A	G	11	GENIC	homozygous	114841063
13	113700145	113700146	T	C	14	GENIC	homozygous	114453357
13	113700688	113700689	A	G	22	GENIC	homozygous	114453359
13	113701371	113701372	C	T	8	GENIC	homozygous	115197966
13	113701684	113701685	T	C	20	GENIC	homozygous	114841067
13	113702403	113702404	A	G	16	GENIC	homozygous	115197967
13	113703265	113703266	C	T	8	GENIC	homozygous	115079303
13	113706104	113706105	T	C	9	GENIC	homozygous	115089051
13	113706236	113706237	G	T	16	GENIC	homozygous	115197968
13	113707726	113707727	A	G	17	GENIC	homozygous	115197969
13	113707788	113707789	T	C	18	GENIC	homozygous	115197970