chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	1476099	1476100	C	G	23	GENIC	heterozygous	147407357
9	1488626	1488627	G	C	8	GENIC	homozygous	403253318
9	1488626	1488627	G		8	GENIC	heterozygous	403253319
9	1491020	1491021	A		10	GENIC	heterozygous	403253323
9	1491020	1491021	A	T	10	GENIC	homozygous	403253324
9	1491022	1491023	A		10	GENIC	heterozygous	403253325
9	1491022	1491023	A	T	10	GENIC	homozygous	403253326
9	1491024	1491025	A		10	GENIC	heterozygous	403253327
9	1491024	1491025	A	T	10	GENIC	homozygous	403253328
9	1495378	1495379	G	T	44	GENIC	possibly homozygous	138483307
9	1484899	1484900	A	C	38	GENIC	homozygous	138483299
9	1486522	1486523	T	C	35	GENIC	homozygous	138483300
9	1489457	1489458	C	T	33	GENIC	homozygous	138483302
9	1490439	1490440	C	T	43	GENIC	homozygous	138483303
9	1493880	1493881	A	G	39	GENIC	homozygous	138483304
9	1493945	1493946	G	A	48	GENIC	homozygous	138483305
9	1494349	1494350	T	C	44	GENIC	homozygous	138483306
9	1496360	1496360		CCTCCTGTAGGGATGACTCCATGAGTGTCCTCCTATAGGGATGACCCCATTATTGTCCTTCTGTAGGGATGACCACATAAAGTGC	28	GENIC	homozygous	138441667
9	1486528	1486533	TTTCC		35	GENIC	homozygous	138441664
9	1490019	1490019		CTCCCTT	44	GENIC	homozygous	138441665
9	1493812	1493812		AGTT	35	GENIC	homozygous	138441666