chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	60685849	60685850	A	T	23	GENIC	homozygous	48745259
14	60686143	60686144	A	G	28	GENIC	homozygous	48745261
14	60686722	60686723	T	A	26	GENIC	homozygous	48745263
14	60687764	60687765	G	C	31	GENIC	homozygous	48745265
14	60688357	60688358	G	C	38	GENIC	homozygous	48745267
14	60690342	60690343	T	C	27	GENIC	homozygous	48745271
14	60692462	60692463	T	TAAA	22	GENIC	homozygous	48745273
14	60694448	60694449	G	A	13	GENIC	homozygous	48745275
14	60695992	60695993	A	C	16	GENIC	homozygous	48745279
14	60696274	60696275	G	T	19	GENIC	homozygous	48745281
14	60698134	60698137	AAA	---	19	GENIC	possibly homozygous	48745283
14	60698148	60698149	A	T	18	GENIC	homozygous	49288751
14	60698191	60698192	C	G	20	GENIC	homozygous	48745285
14	60700281	60700282	A	-	10	GENIC	homozygous	48745287
14	60703418	60703419	C	T	22	GENIC	homozygous	48745289
14	60704772	60704773	G	C	35	GENIC	homozygous	48745291
14	60704874	60704875	C	CTG	16	GENIC	possibly homozygous	49310884
14	60704876	60704877	C	CTG	13	GENIC	possibly homozygous	49310885
14	60704898	60704899	C	CTGTG	6	GENIC	heterozygous	49310886
14	60704898	60704899	C	CTGTGTG	6	GENIC	heterozygous	49310887
14	60705559	60705560	A	G	37	GENIC	homozygous	48745299
14	60705673	60705674	G	A	35	GENIC	possibly homozygous	48745301
14	60706301	60706302	G	-	19	GENIC	homozygous	48745303
14	60707096	60707099	AAA	---	17	GENIC	heterozygous	48745305
14	60707097	60707099	AA	--	17	GENIC	possibly homozygous	48745307
14	60708692	60708693	T	C	27	GENIC	homozygous	48745309
14	60709873	60709874	G	GTT	20	GENIC	homozygous	48745313
14	60710671	60710672	A	G	23	GENIC	homozygous	48745317
14	60707814	60707818	TAGA	----	5	GENIC	homozygous	49005888
14	60710422	60710423	G	GA	17	GENIC	homozygous	48745315