chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90559659	90559660	C	T	25	INTERGENIC	homozygous	51736982
10	90560123	90560124	G	T	29	INTERGENIC	homozygous	51736984
10	90560177	90560178	C	T	36	INTERGENIC	homozygous	51736986
10	90560356	90560360	CCCC	----	13	INTERGENIC	homozygous	51736988
10	90560374	90560375	T	C	22	INTERGENIC	homozygous	51736990
10	90560748	90560749	C	A	17	INTERGENIC	homozygous	51736992
10	90560941	90560942	A	C	19	INTERGENIC	heterozygous	52072807
10	90561398	90561399	T	C	33	INTERGENIC	homozygous	51736994
10	90561410	90561411	C	CA	17	INTERGENIC	homozygous	51736996
10	90561625	90561626	C	T	33	INTERGENIC	homozygous	51736998
10	90561646	90561647	C	G	33	INTERGENIC	homozygous	51737000
10	90562239	90562240	G	T	33	INTERGENIC	homozygous	51737002
10	90562346	90562347	T	-	17	INTERGENIC	heterozygous	52072809
10	90562481	90562482	G	T	33	INTERGENIC	homozygous	51737004
10	90562723	90562724	T	C	41	INTERGENIC	heterozygous	51737006
10	90562728	90562729	C	CT	18	INTERGENIC	possibly homozygous	52072811
10	90562729	90562730	T	-	18	INTERGENIC	heterozygous	51928252
10	90564601	90564602	A	G	41	INTERGENIC	homozygous	51737010
10	90564647	90564648	C	T	40	INTERGENIC	homozygous	51737012
10	90564681	90564682	A	G	49	INTERGENIC	homozygous	51737014
10	90564747	90564748	T	C	37	INTERGENIC	homozygous	51737016
10	90564832	90564833	C	T	13	INTERGENIC	homozygous	51737017
10	90565116	90565117	A	G	18	INTERGENIC	homozygous	51737019
10	90565125	90565129	GCTG	----	13	INTERGENIC	homozygous	51737021
10	90565198	90565199	G	A	23	INTERGENIC	homozygous	51737023
10	90565243	90565244	T	C	27	INTERGENIC	homozygous	51737025
10	90565277	90565278	C	T	30	INTERGENIC	homozygous	51737027
10	90565299	90565300	C	T	30	INTERGENIC	homozygous	51737029
10	90565426	90565427	A	T	44	INTERGENIC	homozygous	51737031
10	90565475	90565476	C	T	50	INTERGENIC	homozygous	51737032
10	90565869	90565870	G	A	16	INTERGENIC	homozygous	51737034