chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	1484899	1484900	A	C	48	GENIC	homozygous	138483299
9	1486522	1486523	T	C	26	GENIC	homozygous	138483300
9	1486528	1486533	TTTCC		27	GENIC	homozygous	138441664
9	1489457	1489458	C	T	41	GENIC	homozygous	138483302
9	1490019	1490019		CTCCCTT	51	GENIC	possibly homozygous	138441665
9	1490439	1490440	C	T	41	GENIC	homozygous	138483303
9	1493812	1493812		AGTT	55	GENIC	homozygous	138441666
9	1493880	1493881	A	G	48	GENIC	homozygous	138483304
9	1493945	1493946	G	A	41	GENIC	homozygous	138483305
9	1494349	1494350	T	C	59	GENIC	possibly homozygous	138483306
9	1495378	1495379	G	T	58	GENIC	possibly homozygous	138483307
9	1496360	1496360		CCTCCTGTAGGGATGACTCCATGAGTGTCCTCCTATAGGGATGACCCCATTATTGTCCTTCTGTAGGGATGACCACATAAAGTGC	19	GENIC	possibly homozygous	138441667
9	1488921	1488922	C	A	10	GENIC	heterozygous	145214507