chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	137357344	137357345	A	C	16	GENIC	homozygous	114022986
5	137357457	137357458	T	G	18	GENIC	homozygous	114022987
5	137358071	137358072	C	T	21	GENIC	homozygous	114022989
5	137358221	137358222	C		16	GENIC	homozygous	128244389
5	137358586	137358587	A	T	17	GENIC	homozygous	114022991
5	137358592	137358593	C	G	17	GENIC	homozygous	114022993
5	137359187	137359188	A	C	28	GENIC	homozygous	114022995
5	137359453	137359454	C	T	28	GENIC	homozygous	114022997
5	137359479	137359483	CCCT		29	GENIC	homozygous	128244390
5	137359484	137359492	TCCTCAGC		29	GENIC	homozygous	128244391
5	137359673	137359674	A	G	22	GENIC	homozygous	114022999
5	137359676	137359677	T	C	22	GENIC	homozygous	114023001
5	137359846	137359847	G	T	17	GENIC	homozygous	114023002
5	137359873	137359874	G	T	18	GENIC	homozygous	114536456