chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	135446592	135446593	A	C	29	GENIC	homozygous	114144467
5	135446596	135446598	AT		29	GENIC	homozygous	128242411
5	135449648	135449648		TC	26	GENIC	homozygous	128242412
5	135449328	135449329	T	C	14	GENIC	homozygous	114017987
5	135450470	135450471	C	T	3	GENIC	homozygous	114017988
5	135451781	135451782	A	G	18	GENIC	homozygous	114017989
5	135453470	135453471	A	T	24	GENIC	homozygous	114017990
5	135453547	135453548	G	A	19	GENIC	homozygous	114017991
5	135453968	135453969	A	G	17	GENIC	homozygous	114017992
5	135455276	135455277	C	T	29	GENIC	homozygous	114017993
5	135456857	135456858	C	A	23	GENIC	homozygous	114017994
5	135457522	135457522		A	17	GENIC	homozygous	128242413
5	135457612	135457614	AA		19	GENIC	homozygous	128242414
5	135460850	135460851	C	T	13	GENIC	homozygous	114017995
5	135461372	135461373	T	G	29	GENIC	homozygous	114017996
5	135461516	135461517	A		21	GENIC	homozygous	128242415
5	135461943	135461943		T	21	GENIC	homozygous	128242416
5	135463891	135463892	G	A	22	GENIC	homozygous	114017998
5	135464035	135464036	G	A	18	GENIC	homozygous	114017999
5	135464554	135464555	A	G	32	GENIC	homozygous	114018000
5	135465138	135465138		T	24	GENIC	homozygous	128242417
5	135467255	135467256	T	C	18	GENIC	homozygous	114018001
5	135468794	135468795	T	G	21	GENIC	homozygous	114018002
5	135469795	135469796	A	G	16	GENIC	homozygous	114018003
5	135470198	135470199	G	A	18	GENIC	homozygous	114018004
5	135471437	135471438	A	G	6	GENIC	homozygous	114018005
5	135457530	135457531	T	A	18	GENIC	homozygous	114603282