chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	103118832	103118833	T	C	51	GENIC	homozygous	139366606
13	103120966	103120967	C	T	44	GENIC	homozygous	139366607
13	103130391	103130392	G	A	43	GENIC	possibly homozygous	139366608
13	103130574	103130575	G	A	47	GENIC	homozygous	139366609
13	103131241	103131242	A	G	49	GENIC	homozygous	139366610
13	103134964	103134965	C	T	55	GENIC	homozygous	139366611
13	103137454	103137455	A	C	48	GENIC	possibly homozygous	139366612
13	103139004	103139005	G	A	35	GENIC	homozygous	139366613
13	103140180	103140181	A	G	42	GENIC	homozygous	139366614
13	103141989	103141991	AC		42	GENIC	homozygous	139190564
13	103148647	103148648	A	G	37	GENIC	homozygous	139366615
13	103152524	103152525	T	C	58	GENIC	homozygous	139366616