chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	24655608	24655609	A	G	12	GENIC	homozygous	47060221
17	24658383	24658384	C	T	28	GENIC	homozygous	47060222
17	24658712	24658713	G	A	28	GENIC	possibly homozygous	47060223
17	24658953	24658954	G	A	17	GENIC	possibly homozygous	47060224
17	24659323	24659324	C	CTGTT	1	GENIC	homozygous	47060227
17	24659497	24659498	A	G	10	GENIC	heterozygous	47060228
17	24659565	24659566	A	G	9	GENIC	homozygous	47060229
17	24659967	24659968	G	T	13	GENIC	possibly homozygous	47060230
17	24660017	24660018	G	C	18	GENIC	possibly homozygous	47060231
17	24661306	24661307	A	G	13	GENIC	possibly homozygous	47060232
17	24662640	24662641	T	A	2	GENIC	homozygous	47060233
17	24662774	24662775	C	A	24	INTERGENIC	homozygous	47060234
17	24662785	24662786	A	AT	18	INTERGENIC	homozygous	47060235
17	24663285	24663286	T	C	13	GENIC	heterozygous	47060236
17	24663297	24663298	T	C	10	GENIC	homozygous	47060237
17	24664277	24664278	C	A	20	GENIC	heterozygous	47060238
17	24664526	24664527	G	A	19	INTERGENIC	heterozygous	47060239
17	24664629	24664636	ATCATGC	-------	3	INTERGENIC	homozygous	47060240
17	24664721	24664722	C	T	7	INTERGENIC	homozygous	47060241
17	24664783	24664784	A	G	11	INTERGENIC	homozygous	47060242
17	24665132	24665133	T	-	2	INTERGENIC	homozygous	47060243
17	24665139	24665140	T	G	3	INTERGENIC	homozygous	47384630
17	24665384	24665385	G	C	15	INTERGENIC	homozygous	47060245
17	24666229	24666230	T	C	26	INTERGENIC	possibly homozygous	47060247
17	24666550	24666551	G	T	30	INTERGENIC	possibly homozygous	47060248
17	24667650	24667651	T	TC	14	INTERGENIC	homozygous	47060250