iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

Rnf123

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3715103	snp	C/T	0.444444	0.157135	upstream-variant-2KB	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108080055	GACTACTGTGATGGG[C/T]ACCACACCTCTACAG	84585
rs4227915	snp	C/G	0.48	0.0979796	intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108052431	TGACCTGACCCACCC[C/G]CTGGTTCACTTACAA	84585
rs4227916	snp	A/G	0.436656	0.166311	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	Rnf123, Amigo3	Mm_Celera	9:108052494	AGGCAAGGTAGTGCC[A/G]GGTGCTAGGGGCTCT	84585
rs8240616	in-del	-/A	0.375	0.216506	upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079564	TACCTTGCCTGGAGG[-/A]NNCCTGACCCACATG	84585
rs8240617	in-del	-/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079565	ACCTTGCCTGGAGGN[-/G]NCCTGACCCACATGC	84585
rs8240618	in-del	-/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079566	CCTTGCCTGGAGGNN[-/G]CCTGACCCACATGCA	84585
rs13470922	snp	C/T	0.231111	0.249285	synonymous-codon, downstream-variant-500B, nc-transcript-variant	Rnf123, Amigo3	GRCm38.p3	9:108056048	CCTCCTGGTGCACGG[C/T]CCAACCTCAGAGTGA	84585
rs29590617	snp	A/C	0.484429	0.0868505	intron-variant	Rnf123	GRCm38.p3	9:108064093	CACAGGGGAACGGAT[A/C]TGAGTGGTGATGACA	84585
rs29591029	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Rnf123, Amigo3	Mm_Celera	9:108053108	AGCCAATGGGAACTT[A/G]GGTCCCCGCCCCTGA	84585
rs29600065	snp	C/T	0.432133	0.171253	intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055441	AGCTACAGGCAGACC[C/T]AATCCCTAAGGCTCA	84585
rs29602266	snp	A/C	0.444444	0.157135	intron-variant, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108056139	AAGGGGAGGGAAGGA[A/C]GATGAAGTGGTTCCA	84585
rs29603889	snp	C/T	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime, intron-variant	Rnf123, Mst1	GRCm38.p3	9:108079352	GGCCAAACCGCGTGC[C/T]CGCTCGAGCGCTGCT	84585
rs29694349	snp	A/G	0.49827	0.0293608	intron-variant	Rnf123	GRCm38.p3	9:108056720	TGAATCTAAACCACC[A/G]GCAGGTAGCCAGGAA	84585
rs29736527	snp	C/T	0.48	0.0979796	upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108081125	GTTAAAGTACTAATG[C/T]GCTCATGCTCACCAC	84585
rs29741418	snp	C/T	0.465374	0.126941	intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054366	TCAGGATGGTAGCAT[C/T]GCTGTGTTGGCTGAT	84585
rs29743766	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108058496	CGGGGTATGTATCCC[C/T]CAAGCTACTTACTGT	84585
rs29791847	snp	G/T	0.375	0.216506	synonymous-codon, downstream-variant-500B, upstream-variant-2KB, utr-variant-5-prime	Mst1, Mir7088, Rnf123	Mm_Celera	9:108081591	GCTTCCAGATTATGT[G/T]CGGACCTGCATTATG	84585
rs29795241	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108060439	TCTCAGAGTCTCTAC[C/T]AGGATTAAGTGATGG	84585
rs29825851	snp	G/T	0.5	0	intron-variant	Rnf123	Mm_Celera	9:108063781	GGACGGGGCAGGGGG[G/T]GTCATGCCTCCATCC	84585
rs29830998	snp	A/G	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108064955	GCTGGGATTAAAGGC[A/G]TGAGCCACCACGCCT	84585
rs29841586	snp	A/C	0.497778	0.0332592	intron-variant	Rnf123	Mm_Celera	9:108065527	AGTCTCTTGTGCCCG[A/C]GGAAGGCACTGCTGG	84585
rs29880471	snp	C/T	0.459184	0.136902	intron-variant	Rnf123	GRCm38.p3	9:108059059	GATTAAGGCATAGAT[C/T]CACTGTGGGGATTGG	84585
rs29894165	snp	A/G	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108077254	ACAGCTGGGAGCCTA[A/G]TGAGAATAGGACACC	84585
rs29930943	snp	C/T	0.429688	0.173817	intron-variant	Rnf123	GRCm38.p3	9:108058123	GGGCTACCAGCCTCT[C/T]TGGAGCCATCACCAG	84585
rs29933460	snp	A/G	0.5	0	intron-variant	Rnf123	GRCm38.p3	9:108075866	AGACTTAAAACTACT[A/G]CCTGTGGAGCTAACA	84585
rs29946565	snp	A/C	0.48	0.0979796	intron-variant	Rnf123	Mm_Celera	9:108059339	GTCTTGCTACAATGG[A/C]AAGCTACTCTGCCTG	84585
rs29982935	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108067244	TTTCCTAGGAACTGA[C/T]TTACACAGGACTACT	84585
rs29983208	snp	C/T	0.48	0.0979796	intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	GRCm38.p3	9:108078327	ATTAGTTTTCTTGCA[C/T]GCGTGCACGCGCTCA	84585
rs29986886	snp	C/T	0.484429	0.0868505	intron-variant, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108056016	CCAGTTCCCAGGAGG[C/T]CAGCAGTCCCCAACA	84585
rs30029385	snp	C/T	0.375	0.216506	intron-variant	Rnf123	Mm_Celera	9:108061265	ACGTTGTTGAAGAAA[C/T]GGAGAACCGGGACTA	84585
rs30037645	snp	A/G	0.465374	0.126941	intron-variant, utr-variant-5-prime	Rnf123, Amigo3	Mm_Celera	9:108053268	AGCGTTGTGCCTCTC[A/G]AGCCATGGGCCATAG	84585
rs30124349	snp	A/G	0.375	0.216506	intron-variant	Rnf123	Mm_Celera	9:108077468	AGAGAAAAAAGGCAC[A/G]TGGTCAGAGCAGCTC	84585
rs30135775	snp	A/T	0.391111	0.206368	intron-variant	Rnf123	Mm_Celera	9:108056343	GCTGAGGTGCGGGAC[A/T]TCTAGATCCTTACCA	84585
rs30178216	snp	A/G	0.375	0.216506	intron-variant, downstream-variant-500B, upstream-variant-2KB	Mst1, Mir7088, Rnf123	Mm_Celera	9:108081762	CCCAGTGTGCACTGT[A/G]GTAAGAATCTTTGTC	84585
rs30180698	snp	A/G	0.48	0.0979796	intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108054471	GCACCACAACCAGAC[A/G]CTTGAGTACAATGTG	84585
rs30217128	snp	C/T	0.375	0.216506	missense, nc-transcript-variant	Rnf123	Mm_Celera	9:108066317	CGGGGGTTGGAAGCT[C/T]TGTATTCATCCCAAT	84585
rs30223385	snp	C/G	0.32	0.24	intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055394	GCATACACACCTACA[C/G]GACCCTCCTACAGAG	84585
rs30227658	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108060954	CTATTCAACATAGCA[C/T]TGGGGATCACAGCCA	84585
rs30277324	snp	A/G	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108064936	CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA	84585
rs30278931	snp	A/G	0.498615	0.0262793	intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108053412	ATCAGGTATACTACT[A/G]TGCATGTTGGGTGCT	84585
rs30282838	snp	A/G	0.277778	0.248452	intron-variant	Rnf123	Mm_Celera	9:108066556	GCAGGCTGAGGTGGC[A/G]GATGCCCAGGCTGCA	84585
rs30326944	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108059656	AGATCGTGAATGGCC[C/T]CATCACCTGGGAGTT	84585
rs30333350	snp	C/T	0.5	0	intron-variant	Rnf123	Mm_Celera	9:108071359	CCTCACCCACCCCAC[C/T]CCTGAGAACACCTCC	84585
rs30380920	snp	A/C	0.498615	0.0262793	intron-variant	Rnf123	GRCm38.p3	9:108057039	GCATTAAGAATGCAG[A/C]GACGCCTGCCTAAGA	84585
rs30382918	snp	A/C/T	0.375	0.216506	intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108054507	GCAAAAGGCTCGCCC[A/C/T]GAGCCAGAGACTTTC	84585
rs30427123	snp	A/T	0.48	0.0979796	intron-variant	Rnf123	GRCm38.p3	9:108071778	TAAATAAGTCTTTTT[A/T]AAAAATGATTGCTAC	84585
rs30468021	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108062504	TCCCTCCCAGTATAC[C/T]TAGGACCCTGTGCAA	84585
rs30524227	snp	C/T	0.375	0.216506	intron-variant, nc-transcript-variant, upstream-variant-2KB	Mst1, Mir7088, Rnf123	Mm_Celera	9:108081543	GAGTAACAGGGGCCA[C/T]GAGGCCTCAGGCCCT	84585
rs33279253	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB, synonymous-codon, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108051215	TGAGTCATGCATCGT[A/G]GGCTGGCGCTGCCGT	84585
rs33280265	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108051482	AGGGCTGGCCAAGCA[C/T]CCACTTTGCCATCAG	84585
rs33280267	snp	C/T	0.231111	0.249285	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108051805	TGGGTAAACAGGGCC[C/T]GGTCTGCGGCTGATG	84585
rs33280269	snp	A/G	0.124444	0.216185	missense, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108051865	GAGGACATGGCGCTT[A/G]TGTTGGCTGCCTTGT	84585
rs33280271	snp	C/T	0.132653	0.220748	intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108051995	GAGTGCTACCTCGTG[C/T]GTCCTAATTTGCCTC	84585
rs33280273	snp	A/G	0.124444	0.216185	synonymous-codon, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052112	GCAGAGGTCCTCTTC[A/G]TTGGTGGGCTACAGG	84585
rs33281005	snp	C/G	0.142012	0.225474	intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108052166	GATCCTTACCCCTGT[C/G]CTGGTGTTTACAGAT	84585
rs33281007	snp	C/G	0.231111	0.249285	intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108052343	CATCAGGGCCCCTGT[C/G]GTCTGAGAACTCAGT	84585
rs33281009	snp	A/C	0.124444	0.216185	intron-variant, upstream-variant-2KB	Rnf123, Amigo3	Mm_Celera	9:108052840	CCCCAGAACCTCACA[A/C]GTCGTCGTCCGACGT	84585
rs33281011	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Rnf123, Amigo3	GRCm38.p3	9:108053010	GCTTCCAGCCAAGCA[A/G]ACTGGGACACTGGGG	84585
rs33281216	snp	C/T	0.124444	0.216185	intron-variant	Rnf123	Mm_Celera	9:108058152	AGGGCTGGTCTAACC[C/T]GAACACTCACTTTGG	84585
rs33281218	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108058883	GGGCAATGAAGACTG[C/T]GGCCGGGAATAAAGG	84585
rs33281220	snp	A/G	0.465374	0.126941	intron-variant	Rnf123	Mm_Celera	9:108059117	GCTCTAACTCATTCT[A/G]GAACATGCCTGGTGA	84585
rs33281222	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108059219	AGGCACAAGACAAGT[A/G]AGGGCCCGCCAGCTT	84585
rs33282025	snp	C/T	0.231111	0.249285	intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108053526	GTTGAGCTGTGCGGG[C/T]CGTGGGTTACAGGAC	84585
rs33282027	snp	C/T	0.124444	0.216185	intron-variant, missense	Rnf123, Amigo3	Mm_Celera	9:108053690	TCCTGGGCCATGGTG[C/T]GTTCACCAATGCCAG	84585
rs33282029	snp	C/T	0.475309	0.108333	intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108054168	GTCCCGAGTGCGCTT[C/T]TTTGAGCACAGCCGG	84585
rs33282031	snp	A/G	0.124444	0.216185	intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054342	TGAGCTGCTTGTGGC[A/G]CCAGCCTCTCAGGAT	84585
rs33282405	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108059802	CTCAATGGTCCGTAG[A/G]CAGACACGCAGTAAC	84585
rs33282407	snp	C/G	0.165289	0.235211	intron-variant	Rnf123	Mm_Celera	9:108059853	CTCCTGCAGGAGGCA[C/G]AGAGGAGGCATTTAC	84585
rs33282409	snp	A/G	0.260355	0.249785	intron-variant	Rnf123	GRCm38.p3	9:108059923	AAAGGCCTACCCAGG[A/G]CAGTGGCCTCACAAC	84585
rs33282410	snp	A/G	0.124444	0.216185	intron-variant	Rnf123	Mm_Celera	9:108060236	TTTCTGAAGCTGAAG[A/G]TCATGGAGCAGAGAC	84585
rs33282412	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108060725	GGCAGCTGTAGTCCA[A/G]GAAAGCACTCACACT	84585
rs33282413	snp	A/G	0.345679	0.230967	intron-variant	Rnf123	GRCm38.p3	9:108061909	TATGGCCTCATGGCC[A/G]TATCTCTCACCTGAC	84585
rs33282965	snp	A/G	0.142012	0.225474	intron-variant, missense	Rnf123, Amigo3	Mm_Celera	9:108054895	GGCTCAGAGGGTCTC[A/G]TGATGAGCTAGACTG	84585
rs33282967	snp	C/T	0.486111	0.0821678	intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055157	CCTGGCATCAGAGTC[C/T]GGGGACCACCCCCAG	84585
rs33282970	snp	A/G	0.244898	0.249948	intron-variant, utr-variant-3-prime	Rnf123, Amigo3	GRCm38.p3	9:108055696	TAAAAGTGGTACATG[A/G]TCATCGCTGGGCCTT	84585
rs33282971	snp	C/T	0.32	0.24	intron-variant, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055895	TTTACACATCACCAG[C/T]TACTCTTTGCCTCAG	84585
rs33283375	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108062002	TCGTTTCTGCCAGTG[C/T]TGACCAGTGGTGACC	84585
rs33283377	snp	A/G	0.32	0.24	intron-variant	Rnf123	Mm_Celera	9:108062087	GGGGTCTGAGCTAGT[A/G]TGAGCATCCAGGACA	84585
rs33283379	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108062139	ATAGCTGGCTAGGCC[C/T]GAGGCTTTGGTGACA	84585
rs33283380	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108062401	TCAGCCAGCCTTGCT[C/T]TTAACACTCAGTGCA	84585
rs33283382	snp	C/T	0.231111	0.249285	synonymous-codon, nc-transcript-variant	Rnf123	GRCm38.p3	9:108062574	TACCCTCTTAGGGCA[C/T]CGACGGAGCTTGTCC	84585
rs33283966	snp	C/T	0.142012	0.225474	synonymous-codon, downstream-variant-500B, nc-transcript-variant	Rnf123, Amigo3	Mm_Celera	9:108056054	TGAGGTTGGGCCGTG[C/T]ACCAGGAGGCGTACC	84585
rs33283971	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108057225	AGTTCTGAGTCACAT[A/G]CCTGTCGGGCAGATG	84585
rs33283973	snp	A/T	0.336735	0.234472	intron-variant, downstream-variant-500B	Rnf123	GRCm38.p3	9:108057562	AAGGAAGAACTTGCT[A/T]TGTGAATCTACACAA	84585
rs33284124	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108063024	GCCCTCAACTGGGGA[A/G]CACAACACGGCATGA	84585
rs33284126	snp	C/G	0.132653	0.220748	intron-variant	Rnf123	Mm_Celera	9:108063352	TCTTATCCTCAGACT[C/G]TGCTTCCTGTGCCCT	84585
rs33284129	snp	C/T	0.260355	0.249785	intron-variant	Rnf123	Mm_Celera	9:108064126	GGCAGGCTGGGCAGG[C/T]GGGCTTGCACAGCTT	84585
rs33284131	snp	C/T	0.142012	0.225474	intron-variant	Rnf123	GRCm38.p3	9:108064434	CCTTGCCATCTCAGC[C/T]TCCGGCAGCCCCTCG	84585
rs33284945	snp	G/T	0.244898	0.249948	intron-variant, downstream-variant-500B	Rnf123	GRCm38.p3	9:108057682	CCCTCTCTGCAAGCT[G/T]CACAGCCCAAGGTCT	84585
rs33284964	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108065548	GCACTGCTGGCTAAA[C/T]AGGAGATCAGATACA	84585
rs33284966	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	Mm_Celera	9:108065573	GATACAGCCTAGCAG[A/G]TCACCCTGTCTCAAC	84585
rs33284968	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108065609	AGAGAGTCTTGGGCA[C/T]CCTCTGGTGGACACA	84585
rs33284972	snp	A/G	0.426035	0.177515	intron-variant	Rnf123	GRCm38.p3	9:108067311	ACCAGGGCAGAAGAG[A/G]CCCCAGGTGCCCGGT	84585
rs33285884	snp	C/T	0.132653	0.220748	intron-variant	Rnf123	Mm_Celera	9:108067793	GAGAGAGACCAGCTT[C/T]GGCCTCCTGGTCAGT	84585
rs33285886	snp	A/G	0.231111	0.249285	intron-variant, synonymous-codon	Rnf123	Mm_Celera	9:108068100	AGGTATTACATGGCA[A/G]ATCTGTCTGGCAACA	84585
rs33285888	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108068605	GTATACCTTGCGCTG[C/T]GGCAAAGGGCAGGCA	84585
rs33285890	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108068613	TGCGCTGCGGCAAAG[A/G]GCAGGCACTAGTAAA	84585
rs33285892	snp	G/T	0.32	0.24	intron-variant	Rnf123	GRCm38.p3	9:108068905	GGCAGGTAACACGCT[G/T]AGCACCCGAGGCCCC	84585
rs33285893	snp	C/T	0.124444	0.216185	intron-variant	Rnf123	Mm_Celera	9:108069487	CATTTTTATGCTTAC[C/T]TGCTCAATGGAGACA	84585
rs33286795	snp	A/G	0.32	0.24	intron-variant	Rnf123	GRCm38.p3	9:108069580	TGTGTACACACCACA[A/G]CAGCTAGGCCTGCCA	84585
rs33286797	snp	C/T	0.32	0.24	synonymous-codon, nc-transcript-variant	Rnf123	GRCm38.p3	9:108069720	CACAGACTCCTTGAA[C/T]GACAGGCTGATGGCT	84585
rs33286799	snp	A/G	0.231111	0.249285	synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108069795	AGTGCCCAGTGACAC[A/G]CCATTCCTGGGAGAG	84585
rs33286801	snp	C/G	0.124444	0.216185	intron-variant	Rnf123	Mm_Celera	9:108070113	GGAAGGACTCGGAGT[C/G]TCCAAACCTCTTGGC	84585
rs33286803	snp	A/G	0.124444	0.216185	intron-variant	Rnf123	Mm_Celera	9:108070156	CCTAAAATTCTTCAC[A/G]GCTGGCCCATGGCTC	84585
rs33287615	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108070674	GTGAATGGAGACCGC[A/G]ACTTGCCTCAAACTC	84585
rs33287617	snp	C/T	0.32	0.24	intron-variant	Rnf123	GRCm38.p3	9:108071508	TTGAGCTCAGCCAAA[C/T]AGTAAGTCCCTGTCA	84585
rs33287619	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108071960	AACCTTACAAGCAGC[C/T]GGATTGGCACAGGCA	84585
rs33690144	snp	A/C	0.444444	0.157135	intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055104	AGAGTGACCAAATGT[A/C]CCATTAACATTACAG	84585
rs33712274	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108077013	GTTTCCAAGTTTCTG[C/T]TACTTGTAACTTCTT	84585
rs33718444	snp	C/T	0.48	0.0979796	intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	Mm_Celera	9:108078337	TTGCATGCGTGCACG[C/T]GCTCACACACACACA	84585
rs33774121	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Rnf123, Mst1	GRCm38.p3	9:108078479	ACTACAGAAACTGCA[C/T]GAACTCCCTGATGCC	84585
rs33896606	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108074685	CCAGCCCCCTCCCCC[C/T]CTTTTTAAAAAAAAA	84585
rs46366468	snp	C/T			intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054699	ACAGTCCTCCATGCT[C/T]AGCACTACGCCACCA	84585
rs48565505	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108061499	GTAAGGTTCAGGGAG[A/G]GCAAAGACTAGCCCA	84585
rs49001764	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108061180	AATCGGAGACATCTA[C/T]ATTCATGGGCTGTTG	84585
rs49392491	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108061359	GCATCCACACGATGG[C/T]TCACATGAAACAGCA	84585
rs49754730	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108061486	GGAGAGGTAGAAGGT[A/G]AGGTTCAGGGAGAGC	84585
rs51181217	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, intron-variant	Rnf123, Mst1	Mm_Celera	9:108079287	CGGCCTCAGCCTCCG[C/G]GACCGGCTCACAACA	84585
rs51407163	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108061367	ACGATGGCTCACATG[A/G]AACAGCACCCAAATA	84585
rs52578713	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108076743	TCTCTCTCTCTCTCT[C/T]TCTTTCTTTCTTTCT	84585
rs107624256	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073957	TGGCCCTGAGAAGAA[A/G]CCAGAATTTGATAGG	84585
rs107666639	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108074157	GAACACACAGGTAGG[A/G]ACATTCATGCTTCAC	84585
rs211897683	in-del	-/CCCAT			intron-variant	Rnf123	Mm_Celera	9:108072296	ACTTGCACCCCCCAC[-/CCCAT]CCCACCCCCTGTTCA	84585
rs212034435	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108069120	GGAGAAAGAATGAGG[A/G]CAGGCGGGCTAAGGT	84585
rs212070496	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108060156	ACAGTGGAAAGAACT[C/G]GATATCCAAGACTAG	84585
rs212251032	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108061648	GCAATATGTGCCAGC[A/G]CCCCAAGAAGGCAGG	84585
rs212294660	snp	A/T			intron-variant, upstream-variant-2KB	Rnf123, Amigo3	Mm_Celera	9:108052829	TTGGGTCTGATCCCC[A/T]GAACCTCACAAGTCG	84585
rs212311926	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108071668	CCAGAGGTCCTGAGT[C/T]CAATTCCCAGCAACC	84585
rs212332026	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108061325	GCTACTCTTTCAGAG[A/G]ACCCAGGTTTGATCC	84585
rs212395188	snp	C/T			intron-variant, nc-transcript-variant, upstream-variant-2KB	Mst1, Mir7088, Rnf123	Mm_Celera	9:108081572	CTGTTGACCTTCCTC[C/T]ATTGCTTCCAGATTA	84585
rs212494988	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108070673	GGTGAATGGAGACCG[C/T]GACTTGCCTCAAACT	84585
rs212517625	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108064044	TGAGAGACATGGCAG[A/G]ATGGGAGGCTTAGGC	84585
rs212556514	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108064966	AGGCGTGAGCCACCA[C/T]GCCTGGCTCGTTGTT	84585
rs212598439	snp	C/G			intron-variant	Rnf123	GRCm38.p3	9:108073390	TCAGTACCTGTTCTA[C/G]TCCTCTACCTAAAAC	84585
rs212673704	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108074003	GGGGTGAGGTGTGTG[G/T]GGGGGGTGAGGGTGG	84585
rs213025604	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108074037	GGAGCCCTCCAGAGC[A/G]GGCTGACCACCCTAC	84585
rs213291191	snp	C/T			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055425	TAGCCCTGCTGTCTT[C/T]AGCTACAGGCAGACC	84585
rs213512629	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108056808	TACGGAGTCCCATCA[C/G]AGCCCACCTCCTGGA	84585
rs213541446	snp	A/G			intron-variant, downstream-variant-500B	Rnf123	Mm_Celera	9:108057771	CCACATCTATAACCC[A/G]CTCTGGGTCCTGATC	84585
rs213625528	in-del	-/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	Rnf123, Mst1	Mm_Celera	9:108078933	ACCTGGAAGCCAACC[-/T]TCCAGACACACACTC	84585
rs213694069	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108060269	AGGACTGGCGCAGGG[C/T]GGGAGTGTAGCCCGG	84585
rs213735895	snp	A/G/T			intron-variant	Rnf123	GRCm38.p3	9:108060828	CAGGAAAGGAGGGCC[A/G/T]GGCTGCGGTGAAAAG	84585
rs213768484	snp	A/G			missense, nc-transcript-variant	Rnf123	Mm_Celera	9:108077368	TGGTGGCTGCGGCGG[A/G]TCCACGGTCAGGAGG	84585
rs214021065	snp	A/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079961	ATGGCAGCCACTGTG[A/G]TCACTAGACTCTTGA	84585
rs214172518	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108076524	ATGGTTGTGAGCCAC[C/T]ATGTGGTTGCTGGGA	84585
rs214268364	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108070401	TGACGTGTCTACTAG[A/G]TGCCCTTGAGTAGAA	84585
rs214397741	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108068445	GATGAAGTCCAACAG[C/T]CTGGCCTAAGCCTGG	84585
rs214477468	snp	C/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Rnf123, Mst1	GRCm38.p3	9:108078552	GCCAAGAGTGGTTAA[C/G]TTTACAAAGTTAAAA	84585
rs214511724	in-del	-/T			intron-variant	Rnf123	Mm_Celera	9:108069474	AAAACCCCTTTGTCA[-/T]TTTTATGCTTACCTG	84585
rs214831943	snp	A/G			intron-variant, utr-variant-3-prime, missense	Rnf123, Amigo3	GRCm38.p3	9:108055591	GCATGCGCCCTGCAC[A/G]CCCACTGGGGTGGGT	84585
rs214868822	snp	A/G			intron-variant, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108056174	CGCAGTTGCTTCTGC[A/G]GCAGAGGCTTCAGGC	84585
rs214884543	in-del	-/G			intron-variant	Rnf123	GRCm38.p3	9:108075027	GAAGAAGAAGAAGAA[-/G]GAGGAGGAGGAGGAG	84585
rs214898730	snp	A/T			intron-variant, downstream-variant-500B, upstream-variant-2KB	Mst1, Mir7088, Rnf123	Mm_Celera	9:108081741	TTAGGCCTGAAGCAG[A/T]ATTCCCCCAGTGTGC	84585
rs215211932	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108077444	GATGCCTGGGTCACC[A/G]ATCAGAAGAGAGAAA	84585
rs215224218	snp	C/T			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108061787	GTGGACCCAGGCAAG[C/T]CTGCGGCTCAGGTGG	84585
rs215264862	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108066267	CAGCCTTGCCAACCC[A/G]GGTCTGCTGTTTCTT	84585
rs215457257	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108062517	ACCTAGGACCCTGTG[C/T]AATACACTTCTGTCC	84585
rs215474676	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108074174	CATTCATGCTTCACC[A/G]CAGGAGAAAAACCTA	84585
rs215689464	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108072522	GGGAGACTAGGCGGA[C/G]ACTAGGGAGGAATGC	84585
rs215855205	in-del	-/T			intron-variant	Rnf123	Mm_Celera	9:108074740	CCAGCCCTGGAACCC[-/T]CACACTATGTTTATA	84585
rs215876247	snp	C/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	Mm_Celera	9:108078045	GTCAGGGACACTATT[C/G]TCCCACGACGTCTCA	84585
rs215889096	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075530	TTGATGCTAGTTATT[A/G]TTTCATAAGTCTCTC	84585
rs215937142	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108065203	TCTCAGGCCCTGTGC[A/G]TTGCTTTTTAAAGTA	84585
rs216007660	in-del	-/CC			intron-variant	Rnf123	Mm_Celera	9:108074679	TCTCTCCAGCCCCCT[-/CC]CCCCCTCTTTTTAAA	84585
rs216083886	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108070527	CCTCTTTGGGAGAGC[A/C]CCTTCCCTCGTGTGT	84585
rs216141403	snp	A/G			upstream-variant-2KB, synonymous-codon, utr-variant-5-prime	Rnf123, Mst1, Mir7088	Mm_Celera	9:108081215	CCTGTTACACACAGC[A/G]GTGCCGGGGCCATGG	84585
rs216288894	snp	C/T			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080083	CAGTAAAGCAGGCAC[C/T]AGGGACTCCATGCAA	84585
rs216340478	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108072884	TAATTCCAGCACTAG[A/G]GATGCTGAGGCAGGA	84585
rs216497372	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108058940	TGTGGGTGGGCTTGT[A/G]TAGCAGAGCCTAGAG	84585
rs216690270	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108068259	AGGGCAGGGACAGAT[A/G]TTCCCACCTGTAGAC	84585
rs216977797	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108061169	ATTAAGGACACAATC[A/G]GAGACATCTATATTC	84585
rs217008469	snp	A/C			intron-variant	Rnf123	GRCm38.p3	9:108073849	AGGTCCTGGCCTAGA[A/C]TCCTACATCTCCTCA	84585
rs217118303	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108067343	CCAGACGCCCTGGTA[C/T]GCTGGGCAGGCCCTC	84585
rs217157999	snp	C/T			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108066400	GGGGCAGAGCACGGG[C/T]GTGTTCTAGGGGCAT	84585
rs217173585	snp	A/G			intron-variant, utr-variant-3-prime	Rnf123	GRCm38.p3	9:108057938	AGCTTCCGCCAAGCT[A/G]GAGGGGTCCTTTCAC	84585
rs217198500	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108065244	TATATAGTCCTGGCT[A/G]ACCTGGAACTCACTA	84585
rs217199598	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108076479	GCTGTCTTCAGACAC[A/T]CCAGAAGAGGGCGTC	84585
rs217220808	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108061603	CTTAAGTCACAGGCA[A/T]GAGGGAATGGCCTGG	84585
rs217271057	in-del	-/A			intron-variant	Rnf123	Mm_Celera	9:108072899	AGATGCTGAGGCAGG[-/A]AAAAAAATGTGAGTT	84585
rs217311448	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108075659	ACCTTGGGGAAGGAT[A/T]CTATCAAGGAACATT	84585
rs217444638	snp	C/T			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108068351	CAGGCAATCCTGTAC[C/T]TCATAGTCCTGGGAA	84585
rs217563921	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108077525	CTCATCTTTGGCCAG[C/T]CACGAAGGTCAGAAG	84585
rs217608408	snp	A/C			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	GRCm38.p3	9:108078374	CACACACACCATATA[A/C]CCGTCTATCCTATGC	84585
rs217649206	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108068829	TAGCCTGGGACATCA[C/G]AACCCTTCCTTCCCA	84585
rs218320393	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108060586	TGGCAGTGGGTGCAT[C/T]ACCACTGAGGCTGGG	84585
rs218333554	in-del	-/G			intron-variant	Rnf123	Mm_Celera	9:108063775	TTGGGGGACGGGGCA[-/G]GGGGGGGTCATGCCT	84585
rs218407989	snp	A/G			intron-variant, missense	Rnf123, Amigo3	Mm_Celera	9:108054641	GGGCCTGCCGCAACC[A/G]TTGCTGGCCCCGGGC	84585
rs218561545	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108062796	AGGCAGTAACGTGTC[C/T]GTGTGCACCAGCGCC	84585
rs218659834	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108061996	CCAAACTCGTTTCTG[C/T]CAGTGTTGACCAGTG	84585
rs218691367	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108064585	CCGACCCCCTGCAGA[C/T]GATCCTCCCACCTCA	84585
rs218716604	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108072147	AAAGGTGGAAATCTC[A/G]GTCTTTCTGGGGAGC	84585
rs218841222	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108056363	GATCCTTACCAGGTA[A/G]CCGTAGGGTAACTAC	84585
rs219119071	in-del	-/C			intron-variant	Rnf123	Mm_Celera	9:108072842	ATAAAAAGGGCCTAT[-/C]AGGCTGGGCATGGTC	84585
rs219289037	in-del	-/G			intron-variant	Rnf123	GRCm38.p3	9:108073985	AGGGGTGGGGAGGTA[-/G]GGGGGGTGAGGTGTG	84585
rs219291271	in-del	-/A			intron-variant	Rnf123	Mm_Celera	9:108076125	AGGAAGGAAGGAAGG[-/A]AAGGAAGGAAGGAAG	84585
rs219349121	snp	C/T			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055012	ACTGCATGTGAGCCT[C/T]GATCCTACTGTAACA	84585
rs219350764	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108065299	AATGGAGATCTTCCT[A/G]CCTCTACCCTCCTGA	84585
rs219380394	snp	C/T			intron-variant, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055788	GAATAGCACATCTTC[C/T]AAGTTTGGGGATTTA	84585
rs219650147	snp	G/T			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080178	AGTGATCTTGGCAAG[G/T]CTGGGGATTGCATAG	84585
rs219711509	snp	G/T			synonymous-codon, nc-transcript-variant	Rnf123	GRCm38.p3	9:108058227	TGGCAGCCGTGTATA[G/T]CGGTACCCAAACCCA	84585
rs219745264	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108060627	ATGATTTGTGAGCAC[A/G]ATCTCAGAGAGGTGG	84585
rs220127468	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	Rnf123, Mst1	Mm_Celera	9:108079127	GCCCCTGCTTGGCCC[C/T]AAGGTCCATAGGACC	84585
rs220133427	in-del	-/GAG			intron-variant, upstream-variant-2KB	Rnf123, Amigo3	Mm_Celera	9:108052895	CATAAGTAAATCTAA[-/GAG]GAGAGCAGCAAGGAC	84585
rs220161938	in-del	-/TGTGTG			intron-variant	Rnf123	Mm_Celera	9:108059538	AGTACAAAAGTTTAA[-/TGTGTG]TGTGTGTGTGTGTGT	84585
rs220361959	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108061368	CGATGGCTCACATGA[A/G]ACAGCACCCAAATAC	84585
rs220457100	in-del	-/GTT			intron-variant	Rnf123	Mm_Celera	9:108061252	ACCGCTTCCAACAAC[-/GTT]GTTGAAGAAACGGAG	84585
rs220551603	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075025	aagaagaagaagaag[A/G]aggaggaggaggagg	84585
rs220684520	in-del	-/ATTAA			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055105	AGTGACCAAATGTCC[-/ATTAA]CATTAACATTACAGA	84585
rs221020364	in-del	-/CTCACA			intron-variant	Rnf123	GRCm38.p3	9:108075555	TCTCTCTCTCTCTCT[-/CTCACA]CACACATACACACAC	84585
rs221146492	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108075767	TCCAGGACAGACAGG[A/G]CCACACAGAGAAACC	84585
rs221177444	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108076828	AACTTCAGTCCTCTT[A/G]CCTTTCCCATTCCCA	84585
rs221212560	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108077699	ATCCCCCCCCCCCCC[C/G]CCCCGGTCATGCCAG	84585
rs221241977	snp	A/G			synonymous-codon, upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052226	CACCAGGGAGGCGGC[A/G]GCCGCCTGGGCAGAT	84585
rs221316717	snp	A/C			intron-variant	Rnf123	GRCm38.p3	9:108074425	CTGGCCTCAAACTCA[A/C]AGAGATCTGCCTTCT	84585
rs221451472	in-del	-/ACACACACAC			intron-variant	Rnf123	GRCm38.p3	9:108075568	CTCTCACACACACAT[-/ACACACACAC]ACACACACACACACA	84585
rs221586654	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108075734	ATGTTTGAGGCCAGC[C/T]TGGCCTACAGAGTAA	84585
rs221671563	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, intron-variant	Rnf123, Mst1	GRCm38.p3	9:108078978	AGAGGATTTAGAGGC[A/G]GAACCTGCGCCTGCC	84585
rs221886125	in-del	-/GGA			upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079559	ACTCCTACCTTGCCT[-/GGA]GGAGGCCTGACCCAC	84585
rs222041096	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073569	CCCCTGCAGAGCCCC[A/G]GGCTGAAGTCAGGAG	84585
rs222110943	in-del	-/C			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080362	ATGTGTCAGTCAAGT[-/C]CAGGCAGGTTCAGAG	84585
rs222214557	in-del	-/AA			intron-variant	Rnf123	Mm_Celera	9:108072898	AGATGCTGAGGCAGG[-/AA]AAAAAAAATGTGAGT	84585
rs222384006	in-del	-/G			intron-variant	Rnf123	Mm_Celera	9:108070107	ACACAGGAAGGACTC[-/G]GGAGTCTCCAAACCT	84585
rs222424533	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108071062	GTCAAGATAGGTGTA[C/T]GGCTACCTCCATCAG	84585
rs222460290	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108072012	GAAACTTATCAGTCT[C/T]AGTGTTTGTCTTACA	84585
rs222603484	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108077020	AGTTTCTGCTACTTG[C/T]AACTTCTTTGTAGAT	84585
rs222634723	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108074341	AAATCACTTTTTTTT[C/T]TTTTCTTTCTCAAGA	84585
rs222646908	snp	A/T			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080248	CACAGAACCCTCCTA[A/T]GTCCTGCCTACCACA	84585
rs222648472	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108066838	GCAGACCCACATAGG[C/T]GTCTTAGGTCACTTA	84585
rs222690656	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108070786	GTCCAATCACCTGGG[A/T]GGAGAAAAATGTGGT	84585
rs222946627	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108077674	TTCTCCTTCCCCCAA[A/C]CCAAAGCACATCCCC	84585
rs223046241	snp	C/G			upstream-variant-2KB, utr-variant-5-prime, intron-variant	Rnf123, Mst1	GRCm38.p3	9:108079424	CAGAAAACCCTCCTC[C/G]GTCTCCTACCAAGGT	84585
rs223110693	snp	A/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080199	GATTGCATAGAGTAG[A/G]CGGGCTCTGCCTCAG	84585
rs223149634	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108058752	AGGCCATTCCACCCC[C/T]ATTCCCAAGGCCCCC	84585
rs223158772	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108070067	GCAGCCTGCCTGGCC[C/T]GCATCCCAGCTGCAT	84585
rs223253027	in-del	-/GGAGAGGGAGGGA			intron-variant	Rnf123	GRCm38.p3	9:108073184	CAGGAAGAGGAAGAG[-/GGAGAGGGAGGGA]GGAGAGGGAAGAGAG	84585
rs223278969	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108067277	ACACAGAAAACCTTT[C/T]ACCCCAAGGACTTCG	84585
rs223506067	in-del	-/G			intron-variant, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108056013	ACCCAGTTCCCAGGA[-/G]GGCCAGCAGTCCCCA	84585
rs223620222	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108066802	CTGGGCTCAGAGCCC[C/T]AAACTGCATACCTCC	84585
rs223639039	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108067711	CCCAGCAGGGGTAAC[C/T]GATGGTCCTAGGTCA	84585
rs223678486	snp	A/C/T			intron-variant	Rnf123	Mm_Celera	9:108076934	TACATTTTGAGATAA[A/C/T]GAAATCCCACTCAAA	84585
rs223843652	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108075812	CTCCCCCCACCTGAA[A/C]ATTATATGTTTATAT	84585
rs223985170	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108063244	TCCCTGTGTCTTCCT[C/T]GTCCAGGAGGGGAGC	84585
rs224015985	in-del	-/TCTCTCTC			intron-variant	Rnf123	Mm_Celera	9:108068763	GCTCCTGACCCATAA[-/TCTCTCTC]TCTCTCTCTCTCTCT	84585
rs224168751	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108072321	TGTTCATTCACTCCT[A/G]TGAGAGTGTGCACAC	84585
rs224191375	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073455	CACTGGCTCCCACGA[A/G]ACAGTTAATCCTCAG	84585
rs224227233	in-del	-/T			intron-variant	Rnf123	GRCm38.p3	9:108073862	GACTCCTACATCTCC[-/T]CAACCACTGATTGAT	84585
rs224236615	snp	A/C			intron-variant	Rnf123	GRCm38.p3	9:108066698	AGAAGCTTCACCCTT[A/C]AAGGGATGGGAAAAC	84585
rs224334928	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108069121	GAGAAAGAATGAGGA[C/G]AGGCGGGCTAAGGTG	84585
rs224433102	in-del	-/AGAGCA			intron-variant	Rnf123	GRCm38.p3	9:108076161	AAGGAAGAAAGAAAG[-/AGAGCA]AGAGAAAGAGAAAGA	84585
rs224505869	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108074616	TGGTTGCTGGGAATT[A/G]AACTCAGTACCTTTG	84585
rs224561563	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108062496	CCCCAGCATCCCTCC[C/T]AGTATACCTAGGACC	84585
rs224608830	snp	C/T			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108063676	GGCCAGGGCTTGCAT[C/T]GGACGCTGTGGTAGA	84585
rs224823755	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108061469	GGCAGGTGAGTTAGG[A/C]AGGAGAGGTAGAAGG	84585
rs224938146	snp	A/C			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108070238	ATAATTCGTGGTGGT[A/C]ACATTCCACTTGCGC	84585
rs224942911	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108057090	GAGAGGAGCAGCACA[C/T]TACTGCCTGGGAGGT	84585
rs224970350	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108060826	CTCAGGAAAGGAGGG[A/C]CTGGCTGCGGTGAAA	84585
rs225026719	in-del	-/G			intron-variant	Rnf123	Mm_Celera	9:108066139	ACAATGGAGGCCCAA[-/G]GCCCCTGAGTGTGGG	84585
rs225198613	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108059530	CACTAATTCAGTACA[A/G]AAGTTTAATGTGTGT	84585
rs225351085	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108068716	GTCCTTCAAGCTGAG[C/T]CCCTTCTAGCGTCTG	84585
rs225394828	in-del	-/AA			intron-variant	Rnf123	GRCm38.p3	9:108072066	CCAGAAACACAAGTT[-/AA]AAAAAAAAAAAAAAA	84585
rs225414098	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108060403	GCAGCCATAATAAAG[G/T]CCCCGTTCCCGCAGT	84585
rs225479364	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108065052	CCTGTACATGCACGG[C/T]GTGCATGCCCAATGG	84585
rs225547577	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108061435	AGAAAGTTAGAAGCG[G/T]CCAAGAAACTCAAGA	84585
rs225626769	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108067970	TTGGGCAGCCTGGTG[A/G]CAGCCAGCAGCTGCC	84585
rs225715613	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108061921	GCCATATCTCTCACC[A/T]GACAGTCTGAGATAG	84585
rs225794136	in-del	-/AG			intron-variant	Rnf123	Mm_Celera	9:108077633	ATGTTCCATGGACCT[-/AG]GCCCTGGCTGCATCT	84585
rs225871209	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108058918	GAGAAGACCTGTCCT[C/T]TGTCAGTGTGGGTGG	84585
rs225893087	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108059914	AGGGTGCAGAAAGGC[C/T]TACCCAGGGCAGTGG	84585
rs226009119	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108057284	CCCACTAGTGTCAAG[A/G]CCAGCTTCATGAAGT	84585
rs226132031	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108066034	GGGACACTGTATGCC[C/G]AAACACAGGAGCCCC	84585
rs226222504	snp	G/T			upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108081108	AACAAAAGATAGGGT[G/T]TGTTAAAGTACTAAT	84585
rs226650254	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108063364	ACTGTGCTTCCTGTG[C/T]CCTTGGGGTGTGGCC	84585
rs226733034	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108058133	CCTCTTTGGAGCCAT[C/T]ACCAGGGCTGGTCTA	84585
rs226886767	in-del	-/A			intron-variant	Rnf123	Mm_Celera	9:108076426	CTTTGAATTTTTTTT[-/A]AAAGATTTATTTATT	84585
rs226935944	snp	G/T			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108054975	TGACCTGCTGGTGGG[G/T]CGTGCTGTGCCTGGT	84585
rs226966391	snp	C/T			intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108054504	TGTGCAAAAGGCTCG[C/T]CCCGAGCCAGAGACT	84585
rs227009074	snp	A/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055187	GGAGTTAATGCAGAT[A/G]TCAGGGTGTGGTATA	84585
rs227179545	snp	C/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052336	TAGGTAGCATCAGGG[C/T]CCCTGTCGTCTGAGA	84585
rs227326494	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108076295	TAATCTAAATACTTA[C/G]GTGCCAGAGGCAGGT	84585
rs227361768	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108077095	AGGCAGAGGCTACAG[G/T]GGCAGAATAGAGGTA	84585
rs227414555	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108057231	GAGTCACATGCCTGT[C/T]GGGCAGATGTCATAT	84585
rs227836376	snp	C/T			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108077777	GCTCTTTCGGGAGAA[C/T]GACATGCCAGTCCCC	84585
rs227858867	in-del	-/AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAA			intron-variant	Rnf123	GRCm38.p3	9:108076035	AAGGAAGAAAGAGAG[lengthTooLong]AGAGAGAGAGAGAGA	84585
rs227895162	snp	C/T			intron-variant, downstream-variant-500B	Rnf123	Mm_Celera	9:108057615	ATCCAGAGACCAAGA[C/T]ACTAGCTTCAAGGCC	84585
rs227900136	snp	A/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108079880	AGAAAAGTATAATCC[A/G]GGGGTCTGGGAAATC	84585
rs228110816	in-del	-/GC			intron-variant	Rnf123	Mm_Celera	9:108068618	TGCGGCAAAGGGCAG[-/GC]ACTAGTAAAGTTGTG	84585
rs228150517	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	Mm_Celera	9:108078054	ACTATTGTCCCACGA[C/T]GTCTCAGTGCCCCAT	84585
rs228309118	in-del	-/AGCACT			intron-variant	Rnf123	GRCm38.p3	9:108073899	CTTCCTGGTGATCAC[-/AGCACT]AGCAGTAGCATCTGC	84585
rs228365296	snp	A/T			upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080912	AAGGCCAACACACTG[A/T]CACCCAAATTCTCAT	84585
rs228499474	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108070173	CTGGCCCATGGCTCC[A/C]GTGAAGACAACAACC	84585
rs228511734	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079726	GCGATGGGATGGATG[C/T]TCCTCGGATGTGCTG	84585
rs228532668	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108068981	CTGCCCTTCCCTGCC[A/T]TCTCCTCACCAGCAG	84585
rs228640111	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108071555	CTGGAGGATGCTTGG[C/T]TGAAGCTCCAGACCA	84585
rs228677397	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108072434	TGAAGATTCCAGGGA[A/C]CAGCATGCTCTGCCC	84585
rs228995432	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073610	CCTCACCCAGCCAGT[A/G]ATGAGGACGGCTGAA	84585
rs229200565	in-del	-/TGTG			intron-variant	Rnf123	GRCm38.p3	9:108059539	AGTACAAAAGTTTAA[-/TGTG]TGTGTGTGTGTGTGT	84585
rs229313675	in-del	-/GCATGCTCT			intron-variant	Rnf123	Mm_Celera	9:108072437	AGATTCCAGGGAACA[-/GCATGCTCT]GCCCTTAGCTCGCAA	84585
rs229509299	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108075898	GATGGCTCAGTGGAT[A/G]AAGGCACTTGCCCTG	84585
rs229551486	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108074837	AACCACTAAAATCAA[G/T]TCATACTATGGAAAA	84585
rs229623697	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108072511	GAAAGTGAGGCGGGA[A/G]ACTAGGCGGAGACTA	84585
rs229749748	in-del	-/AG			intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052129	GGTGGGCTACAGGGC[-/AG]AGAGTGGAGGAGTTG	84585
rs229807806	in-del	-/C			intron-variant, upstream-variant-2KB	Mst1, Rnf123, Mir7088	Mm_Celera	9:108081365	ACTTTGTGTCTGCCA[-/C]CCCCCCCCCCCTTCT	84585
rs229925051	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108066442	CATGTTCTGGTGCCA[C/T]CCCAGAGCCCAGCTC	84585
rs229942556	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108074959	CACATAGTAAGTTCC[A/G]AGATAGCCAGTGATA	84585
rs229946945	snp	A/C			intron-variant	Rnf123	GRCm38.p3	9:108075698	GCACACCTTTAGCTC[A/C]GGCACTAGGGAGGCA	84585
rs229977329	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108065281	CCAGGTTGGCCTTGA[A/G]CTAATGGAGATCTTC	84585
rs229978917	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108076495	CCAGAAGAGGGCGTC[A/C]GATCTTGTTACAGAT	84585
rs229989347	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108059209	GGACTGGGCCAGGCA[C/T]AAGACAAGTGAGGGC	84585
rs230007619	in-del	-/CCA			intron-variant, upstream-variant-2KB	Mst1, Rnf123, Mir7088	Mm_Celera	9:108081366	CTTTGTGTCTGCCAC[-/CCA]CCCCCCCCCCTTCTC	84585
rs230012913	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108067739	TCAGGCCTCAGCTTT[G/T]CTTCCTATGTTTCCT	84585
rs230046844	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108068434	CCCTTACCCATGATG[A/G]AGTCCAACAGCCTGG	84585
rs230820264	snp	A/G			intron-variant, missense	Rnf123	Mm_Celera	9:108068113	CAGATCTGTCTGGCA[A/G]CAGGATACAGGACAT	84585
rs230878262	snp	A/C			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	GRCm38.p3	9:108077938	CAGGTAAGACTGAAC[A/C]ATGCATATTCACACA	84585
rs230880814	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108068902	CCTGGCAGGTAACAC[A/G]CTTAGCACCCGAGGC	84585
rs231000842	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108061673	GGCAGGGGTCCTTAA[A/G]GGTCCAGTGCAACCT	84585
rs231016304	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108060922	TAAGACAAAGATGTC[C/T]ATCTTTGCCATTAAT	84585
rs231025226	in-del	-/G			intron-variant	Rnf123	Mm_Celera	9:108064803	TGCTAATTTTTTTTT[-/G]GTTTGTTTTGGTTTT	84585
rs231080208	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108070436	GCATAGTCCATCCTC[A/G]GGGGGGGGCAGCCCG	84585
rs231100425	snp	C/T			missense, nc-transcript-variant	Rnf123	Mm_Celera	9:108077392	CAGGAGGGGAAAAGA[C/T]GCGGTACAGATAGTC	84585
rs231314186	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108071537	CACCCTTCTCCTTGA[A/G]CACTGGAGGATGCTT	84585
rs231325422	snp	A/G			intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108054708	CATGCTTAGCACTAC[A/G]CCACCAGATGCACCC	84585
rs231357661	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108063067	GGCCTTTGGTTCTGG[C/T]TTGTTTGAGAGTCTC	84585
rs231415003	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108064088	GGGACCACAGGGGAA[C/T]GGATCTGAGTGGTGA	84585
rs231742047	in-del	-/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080299	AGCTGCAATGAGACA[-/G]GCACTCGAGGGCCTC	84585
rs231795098	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108064711	CCTCAGACTGGCCTC[A/T]CTCCCCAGTGTCCTG	84585
rs231963191	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108072586	CATTTAGTCCTTAAC[C/T]GTAAACCTATGGTTC	84585
rs232057139	snp	C/T			intron-variant, downstream-variant-500B	Rnf123	Mm_Celera	9:108057822	TCCTGAGTCAAGGGT[C/T]CAAGGCCAGAAGATA	84585
rs232069977	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108061507	CAGGGAGAGCAAAGA[C/T]TAGCCCAGCAGGCAT	84585
rs232116254	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108057034	CCGCTGCATTAAGAA[C/T]GCAGCGACGCCTGCC	84585
rs232118975	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108067186	CCTTGCTTCCTTACC[A/G]TCTCTGCTCTACGCA	84585
rs232155680	in-del	-/AGG			intron-variant	Rnf123	Mm_Celera	9:108063695	CGCTGTGGTAGAGAA[-/AGG]GGGTCAGAGGCTAGT	84585
rs232497118	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108063773	GGGTTGGGGGACGGG[A/G]CAGGGGGGGTCATGC	84585
rs232561429	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108076720	CTCCCTCCCTCCCTC[C/T]CTCCCTCTCTCTCTC	84585
rs232583970	snp	C/G			intron-variant	Rnf123	GRCm38.p3	9:108073641	GGCAACCCTCTCTCT[C/G]AATACCCCAGTAGTC	84585
rs232702686	snp	C/G			intron-variant, downstream-variant-500B	Rnf123	Mm_Celera	9:108057508	CCTTCCCCACTTGCA[C/G]CTCAATTCCGTCCTA	84585
rs232745626	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108056212	ACACCACTGACCTTT[C/G]CCCCTGTTTTTCCTA	84585
rs232814916	snp	C/T			missense, nc-transcript-variant	Rnf123	GRCm38.p3	9:108066302	TCACTGAAGGAAGCA[C/T]GGGGGTTGGAAGCTT	84585
rs233018077	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108059365	GCCTGTCTCACTGCC[A/G]CTCTGTGACAGTACC	84585
rs233038105	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108060035	TCTCACTATGACCCA[C/T]GCGAGAACCCATTAC	84585
rs233073512	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108060388	TGGTGGGAAAGAAGG[A/G]CAGCCATAATAAAGT	84585
rs233165790	in-del	-/TTTT			intron-variant	Rnf123	GRCm38.p3	9:108074332	ATATAGCAAAATCAC[-/TTTT]TTTTTTTTTTTTTCT	84585
rs233195386	snp	C/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052010	CGTCCTAATTTGCCT[C/T]CCCAAGTCCATGGGG	84585
rs233298320	snp	A/T			intron-variant	Rnf123	GRCm38.p3	9:108061632	GGTGAGTAGGGAAGG[A/T]GCAATATGTGCCAGC	84585
rs233454595	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108074246	GAGCTTGCAGGATAT[G/T]CATGGTGCCTGGATT	84585
rs233485290	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108075634	CCTTTCCAAGTGGAG[A/T]GCAAGGGGGACCTTG	84585
rs233577599	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108058647	TGTGGGCTAAGAACC[C/T]CAAGCCTAATGCCCA	84585
rs233769402	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108060678	GGGAGGAAGCTAAGA[C/T]AGCAGAGAGAGAAGA	84585
rs233861494	snp	C/T			intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054126	TTTTGAACGCGAGTA[C/T]ACATGCTTGGTCTTT	84585
rs234024950	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	Rnf123, Mst1	GRCm38.p3	9:108079022	CCACTCCATTATTGC[C/T]CAGCCCTTCTAAGAG	84585
rs234120061	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108062425	CAGTGCAGTCAGGGC[A/G]GGGACAAGGGAAAAT	84585
rs234426166	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108056507	GTCCCCCCTCCTTGT[C/T]CTGATGGACACACCT	84585
rs234691936	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108070651	GAGAGCAGCGTTAGG[C/T]CCAGCAGGTGAATGG	84585
rs234718649	snp	A/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080084	AGTAAAGCAGGCACC[A/G]GGGACTCCATGCAAC	84585
rs234761058	snp	A/C			intron-variant, upstream-variant-2KB	Mst1, Rnf123, Mir7088	Mm_Celera	9:108081369	TTGTGTCTGCCACCC[A/C]CCCCCCCTTCTCCAG	84585
rs234871336	in-del	-/GAGGGA			intron-variant	Rnf123	Mm_Celera	9:108060773	AGGCAGGGAGGGAGG[-/GAGGGA]GGGGGGAGCGCTGGA	84585
rs234930768	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076863	TGGGGTTCCAGTTAT[A/G]AGCCACACCCTTCAG	84585
rs234954620	in-del	-/AAA			intron-variant	Rnf123	Mm_Celera	9:108072065	CCAGAAACACAAGTT[-/AAA]AAAAAAAAAAAAAAA	84585
rs234970213	snp	C/G			intron-variant	Rnf123	GRCm38.p3	9:108077467	GAGAGAAAAAAGGCA[C/G]GTGGTCAGAGCAGCT	84585
rs234980131	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108077531	TTTGGCCAGCCACGA[A/G]GGTCAGAAGAGCAAC	84585
rs235059882	in-del	-/GAAGGAAGAAAGAAAGAGAGCA			intron-variant	Rnf123	GRCm38.p3	9:108076145	AAGGAAGGAAGGAAG[-/GAAGGAAGAAAGAAAGAGAGCA]AGAGAAAGAGAAAGA	84585
rs235158228	snp	A/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080184	CTTGGCAAGTCTGGG[A/G]ATTGCATAGAGTAGA	84585
rs235246540	snp	C/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055337	CCAGTCTGCTGCCAC[C/G]CAGCCTCCTGAAAGC	84585
rs235761497	in-del	-/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Rnf123, Mst1	Mm_Celera	9:108078701	TTGGCCTTTAGTCAC[-/T]TGCCTGAGCCAGCAC	84585
rs235801673	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108064544	CCCCTATCCTCCATC[C/G]GCTAGATACCTGTAC	84585
rs235802200	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108071700	CATGGTGGCTCACAA[C/T]CATCTGTAATGGGAT	84585
rs235868181	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108073223	agagggagagggagg[G/T]aggagagggagaggg	84585
rs235931700	snp	C/G			intron-variant	Rnf123	GRCm38.p3	9:108074038	GAGCCCTCCAGAGCG[C/G]GCTGACCACCCTACT	84585
rs236108230	snp	A/C/G			intron-variant	Rnf123	Mm_Celera	9:108062797	GGCAGTAACGTGTCT[A/C/G]TGTGCACCAGCGCCC	84585
rs236124158	snp	C/T			intron-variant, utr-variant-3-prime	Rnf123, Amigo3	Mm_Celera	9:108055701	GTGGTACATGATCAT[C/T]GCTGGGCCTTCCCAG	84585
rs236125623	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108072036	TCTTACAAGCAAGAG[A/G]AGCAGAGTTCAGTAC	84585
rs236166012	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108072893	CACTAGAGATGCTGA[A/G]GCAGGAAAAAAAATG	84585
rs236221448	in-del	-/CTCT			intron-variant	Rnf123	Mm_Celera	9:108068790	TCTCTCTCTCTGGGG[-/CTCT]CTCTATTCATGGCCC	84585
rs236305179	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108076554	ATTTGAACTCCGGAC[C/T]TTCGGAAGAGCAGTC	84585
rs236345946	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108068837	GACATCACAACCCTT[C/G]CTTCCCAGGATGCTC	84585
rs236384256	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108059855	CCTGCAGGAGGCACA[A/G]AGGAGGCATTTACTG	84585
rs236384338	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108069926	GTCTGGCTGTGTCTG[A/T]AGACAGAGGGAGGAG	84585
rs236754944	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108063841	TACACGGAGAGAAGC[C/T]GGACCTGGGTCATAC	84585
rs236941390	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108066577	CCAGGCTGCAGCCCT[G/T]CAACCCAGCCAGGAG	84585
rs237042818	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108060595	GTGCATCACCACTGA[A/G]GCTGGGGACAGGGTA	84585
rs237267931	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Rnf123, Mst1	Mm_Celera	9:108078637	AAGGCACAGGTGTGC[C/T]ATCACCACCACCGGC	84585
rs237351778	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108057248	GGCAGATGTCATATA[A/G]ACAAGACAACTTAGA	84585
rs237403323	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108058135	TCTTTGGAGCCATCA[C/T]CAGGGCTGGTCTAAC	84585
rs237493407	in-del	-/A			intron-variant	Rnf123	Mm_Celera	9:108074849	CAATTCATACTATGG[-/A]AAAATATTCATGAAA	84585
rs237517445	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108065661	CAGGAGACTCAGAGA[C/G]TGCTCCTACCCAGCC	84585
rs237536082	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108070820	TCTCTCCAGGAACAT[A/T]GGTTGTCCTGAGACA	84585
rs237570857	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108066814	CCCCAAACTGCATAC[A/C]TCCAAGCCGCAGACC	84585
rs237572903	in-del	-/GGACTCCATGCAACTTCT			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080086	TAAAGCAGGCACCAG[-/GGACTCCATGCAACTTCT]GGAGCGCGTGTAGCA	84585
rs237645108	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108064597	AGACGATCCTCCCAC[C/T]TCAGCAGCTAGAGGG	84585
rs237941899	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073428	CTCTGGAAGGGTTAT[A/G]AATGTGCAGAGCACT	84585
rs238157287	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075748	CCTGGCCTACAGAGT[A/G]AGTTCCAGGACAGAC	84585
rs238189369	in-del	-/A			intron-variant	Rnf123	GRCm38.p3	9:108075242	AGGAGGAGGGGGAGG[-/A]GGGGGAGGAGGAGGA	84585
rs238252072	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108062533	AATACACTTCTGTCC[C/T]AGCACCCACCTGCTG	84585
rs238295807	in-del	-/CTT			intron-variant	Rnf123	Mm_Celera	9:108067999	CCTCCTCCCTTTTGC[-/CTT]CTTTGCTCTGTAAAG	84585
rs238319100	snp	A/G			intron-variant, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055818	AGGCCCCTGCAAGGG[A/G]TGTGGCTGAAAAAGC	84585
rs238370776	in-del	-/A			intron-variant	Rnf123	GRCm38.p3	9:108070435	GCATAGTCCATCCTC[-/A]GGGGGGGGGCAGCCC	84585
rs238420556	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108065221	GCTTTTTAAAGTAAG[A/G]GTCTCACTATATAGT	84585
rs238454705	snp	A/G			intron-variant, utr-variant-3-prime	Rnf123, Amigo3	GRCm38.p3	9:108055632	GTCAGTGCCTGCCCA[A/G]TGATGAGCTGGCAGC	84585
rs238590629	snp	A/G			synonymous-codon, upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052252	CAGATGCAGCGGTCA[A/G]GTGAGCCAGCATCTG	84585
rs238629051	snp	A/G			intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108053550	ACAGGACTTGCCGGT[A/G]GCACTGCCTACCACT	84585
rs238794719	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108067414	CCTGCTGGAGCGATG[A/G]GGCCACCAGGTGGTG	84585
rs238823983	in-del	-/GCATGT			intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052191	CAGATTAGTAAAACG[-/GCATGT]GCCTCTGTTATGCCA	84585
rs238867311	in-del	-/T			intron-variant	Rnf123	Mm_Celera	9:108065363	TGCCTATATTTGCCA[-/T]TCTTGCCCTTGAGTT	84585
rs238981818	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108067333	GTGCCCGGTGCCAGA[C/T]GCCCTGGTATGCTGG	84585
rs239146333	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108069511	GGAGACAGCTAATGG[C/T]ACCCACCTTTAAAAG	84585
rs239236462	in-del	-/GT/GTGT			intron-variant	Rnf123	GRCm38.p3	9:108073995	GGTAGGGGGGGTGAG[-/GT/GTGT]GTGTGTGGGGGGGGT	84585
rs239449896	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108058032	GAGAGGAGCAGAAAT[A/G]GGAGCCCAAGGGAAA	84585
rs239477136	in-del	-/AG			intron-variant	Rnf123	Mm_Celera	9:108064273	GAGCCCCATGGATCT[-/AG]AGTTTCCTGCCGCTT	84585
rs239513778	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108076688	ctttctttctttctt[C/T]cttcctccctccctc	84585
rs239598426	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108071817	TGTAATTTTGCTACT[A/G]TTATGAATCGAACTG	84585
rs239654350	in-del	-/AA			intron-variant	Rnf123	Mm_Celera	9:108075004	ACCTCAAAGAAGAAG[-/AA]GAAGAAGAAGAAGAA	84585
rs239984601	snp	A/G			intron-variant, downstream-variant-500B	Rnf123	GRCm38.p3	9:108057414	AGAGCTCTCGGCCGC[A/G]ACTGGCCTGACATAG	84585
rs240021470	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108058287	AGGTAGGGGCAGGGT[A/G]ACATTTCCTTCCAGC	84585
rs240143654	in-del	-/T			intron-variant	Rnf123	Mm_Celera	9:108074685	CCAGCCCCCTCCCCC[-/T]CTTTTTAAAAAAAAA	84585
rs240396896	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108061893	AAAAATACAATCAGA[A/C]TATGGCCTCATGGCC	84585
rs240400070	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, intron-variant	Rnf123, Mst1	Mm_Celera	9:108079467	TGCCTGATGGTCCAC[C/T]TGTTTCGCCCCCACC	84585
rs240415864	snp	C/T			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080225	CTCAGGGACACCTAA[C/T]GTTTCCACACAGAAC	84585
rs240508803	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108077704	CCCCCCCCCCGCCCC[C/G]GTCATGCCAGCCCTT	84585
rs240549257	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108068020	TGCTCTGTAAAGGGG[C/T]TGGGACTTCTGAACC	84585
rs240570937	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108077097	GCAGAGGCTACAGGG[A/G]CAGAATAGAGGTACA	84585
rs240666643	snp	G/T			intron-variant, utr-variant-3-prime	Rnf123, Amigo3	GRCm38.p3	9:108054927	CTGAGATCTCCTGCT[G/T]CTTGCCCTGCTTGCT	84585
rs240731707	snp	C/T			intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054681	ACTCCAGGAGCTGAG[C/T]GCACAGTCCTCCATG	84585
rs240851385	in-del	-/GTTA			intron-variant	Rnf123	Mm_Celera	9:108077303	CAGGTTCCAGCATCT[-/GTTA]GGTCAGGCCTAACAG	84585
rs240903264	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108064286	CTAGAGTTTCCTGCC[A/G]CTTCCAGCTGACTGT	84585
rs240973320	in-del	-/TGT			intron-variant	Rnf123	GRCm38.p3	9:108074002	GGGGTGAGGTGTGTG[-/TGT]GGGGGGGTGAGGGTG	84585
rs240999158	in-del	-/T			intron-variant	Rnf123	Mm_Celera	9:108076882	ACACCCTTCAGATCG[-/T]TTTTTTCCCCAAAAG	84585
rs241143710	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108068727	TGAGTCCCTTCTAGC[C/G]TCTGACTGAGGGATG	84585
rs241164856	snp	C/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108054976	GACCTGCTGGTGGGG[C/G]GTGCTGTGCCTGGTC	84585
rs241197916	snp	C/T			intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054054	GCTGCCCTGTGACTG[C/T]AGCCTCTACCACCTG	84585
rs241322218	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108066738	CTGAGCTGAGGATTC[C/T]GCACCTTACCCTGCG	84585
rs241547050	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108075783	CCACACAGAGAAACC[C/T]TGTCTTGAAACACCT	84585
rs241563159	in-del	-/A			intron-variant	Rnf123	Mm_Celera	9:108072944	GCTACACAGAGAGGG[-/A]GAAGGGGAGGGAGGA	84585
rs241610698	snp	A/T			intron-variant	Rnf123	GRCm38.p3	9:108075816	CCCCACCTGAAAATT[A/T]TATGTTTATATAGAA	84585
rs241627282	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108073573	TGCAGAGCCCCAGGC[G/T]GAAGTCAGGAGCCAG	84585
rs241662825	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108074342	AATCACTTTTTTTTT[C/T]TTTCTTTCTCAAGAC	84585
rs241665594	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108063450	GGGTTGCACACAGCA[A/G]ACGGTCCCTTAGCAG	84585
rs241668302	in-del	-/CAAA			intron-variant	Rnf123	Mm_Celera	9:108072320	TGTTCATTCACTCCT[-/CAAA]GTGAGAGTGTGCACA	84585
rs241845211	in-del	-/C			intron-variant	Rnf123	Mm_Celera	9:108056494	AGTGATCCCCAGGGT[-/C]CCCCCTCCTTGTCCT	84585
rs241864010	in-del	-/TTT			intron-variant	Rnf123	Mm_Celera	9:108064814	TTTTGTTTGTTTTGG[-/TTT]TTTTTTTTGTTTTTT	84585
rs242009859	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108068288	ACCCAGGTCTGGGAC[A/G]ATAGGCGAGAATCGG	84585
rs242059951	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108059034	TATAATGGCAATTGG[A/G]AAGGGGATTGATTAA	84585
rs242063226	snp	C/T			utr-variant-5-prime, nc-transcript-variant	Rnf123	Mm_Celera	9:108077811	GACGCCATCCCTCAT[C/T]ACTCATGGGCAGTCA	84585
rs242640760	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108070176	GCCCATGGCTCCCGT[G/T]AAGACAACAACCTAG	84585
rs242672918	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108071114	ATAAGCGTAGAGGAT[A/G]GGGCTGAGCTGGGGC	84585
rs242695721	snp	A/C			upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080629	ACTTTTCTTTGGGTC[A/C]GGGATCAGTGACCTT	84585
rs242755695	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108058763	CCCCCATTCCCAAGG[C/T]CCCCTGGAAGACATC	84585
rs242815097	snp	A/G			intron-variant, missense	Rnf123	Mm_Celera	9:108068101	GGTATTACATGGCAG[A/G]TCTGTCTGGCAACAG	84585
rs242966653	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108072270	GATAGACAACTTTTC[C/T]CTCTGGCCTCCACTT	84585
rs242977713	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108067298	AAGGACTTCGGGAAC[C/T]AGGGCAGAAGAGACC	84585
rs243189652	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108074004	GGGTGAGGTGTGTGG[G/T]GGGGGTGAGGGTGGA	84585
rs243228376	snp	C/T			synonymous-codon, nc-transcript-variant	Rnf123	GRCm38.p3	9:108063984	GGTGGCTGCCTGGAG[C/T]TCCAGGGGGTCGATC	84585
rs243228455	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108074947	GTCAACCTGGTCCAC[A/G]TAGTAAGTTCCAAGA	84585
rs243289195	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108074518	TAAAAAAATATTTTA[C/T]TTATATGAATACACT	84585
rs243747074	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108077060	ATGTATTTAACTGAG[A/G]TTTCTCTTATGTAAG	84585
rs243835589	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108064958	GGGATTAAAGGCGTG[A/C]GCCACCACGCCTGGC	84585
rs243949221	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108063706	AGAAAGGGGGTCAGA[A/G]GCTAGTCTGGCTTCC	84585
rs243954536	snp	A/C			intron-variant, upstream-variant-2KB	Rnf123, Amigo3	Mm_Celera	9:108052954	CTGAGGGCTGAAGGC[A/C]TTCTCCCCTAAGTCC	84585
rs244361176	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108076989	AAGAGGTTTGCTTTG[C/T]TTTGCTTTGTTTCCA	84585
rs244364347	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108060237	TTCTGAAGCTGAAGG[C/T]CATGGAGCAGAGACT	84585
rs244530551	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108066920	GTTCTTCCACCACTG[A/G]GATGGGAAAAGGAAT	84585
rs244667503	in-del	-/TAC			intron-variant	Rnf123	GRCm38.p3	9:108075402	ACCCTCACACTGACA[-/TAC]TACATGGAGGCAAAA	84585
rs244822253	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108061378	CATGAAACAGCACCC[A/G]AATACATATGTCAGC	84585
rs244934047	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108060827	TCAGGAAAGGAGGGC[C/T]TGGCTGCGGTGAAAA	84585
rs245186451	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108058931	CTCTGTCAGTGTGGG[C/T]GGGCTTGTGTAGCAG	84585
rs245451815	snp	G/T			intron-variant, utr-variant-3-prime, missense	Rnf123, Amigo3	GRCm38.p3	9:108055576	AACAGAGCCCTCAGG[G/T]CATGCGCCCTGCACA	84585
rs245503601	snp	C/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080082	ACAGTAAAGCAGGCA[C/G]CAGGGACTCCATGCA	84585
rs246029453	snp	C/T			intron-variant, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108056155	GATGAAGTGGTTCCA[C/T]TTACGCAGTTGCTTC	84585
rs246080128	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108065332	GCTGGGATTAACAGT[G/T]TGTGCCATCACAACC	84585
rs246298183	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108073622	AGTAATGAGGACGGC[C/T]GAAGGCAACCCTCTC	84585
rs246354691	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073532	AGCTGCTGGAGATAG[A/G]TTCTGCAAAGGCCCC	84585
rs246403471	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	Mm_Celera	9:108078007	CTTTCCAAACATGGA[C/T]GTTGGGTGGGATTTA	84585
rs246407703	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108063339	TGTAGTATTGATTTC[A/T]TATCCTCAGACTGTG	84585
rs246568769	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108075643	GTGGAGTGCAAGGGG[A/G]ACCTTGGGGAAGGAT	84585
rs246605445	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108076329	TCTCACACCACCTTC[A/G]AGTGAGCGGAGTACC	84585
rs246636404	snp	C/T			intron-variant, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055925	GTGTCCCAAACTAGA[C/T]TCTGAAGTTCATTCT	84585
rs246982144	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108072798	AAGGGCTGGGCAGCT[A/G]CCTAATCCTCTCAGC	84585
rs247179897	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108067839	GAGAAGAGGAAGGCT[A/G]CCTCTTCAGAGAAGA	84585
rs247248006	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108077678	CCTTCCCCCAACCCA[A/T]AGCACATCCCCCCCC	84585
rs247403149	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108060656	GGAGCAGCCAAGAGT[C/G]GGGGAGGGGAGGAAG	84585
rs247412015	in-del	-/TT			intron-variant	Rnf123	GRCm38.p3	9:108076418	AAAAGCAACTTTGAA[-/TT]TTTTTTTTAAAGATT	84585
rs247512261	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108062428	TGCAGTCAGGGCGGG[A/G]ACAAGGGAAAATGTC	84585
rs247571898	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108061647	AGCAATATGTGCCAG[C/T]GCCCCAAGAAGGCAG	84585
rs247574689	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108073738	TGCCTATGCCAGCAG[C/T]ACACAATACATAGTG	84585
rs247576710	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108072443	CAGGGAACAGCATGC[G/T]CTGCCCTTAGCTCGC	84585
rs247690458	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108070671	CAGGTGAATGGAGAC[A/C]GCGACTTGCCTCAAA	84585
rs247722640	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108071599	TTCCTCAGTGAAAAA[A/G]TGATTTCTGGGGCTG	84585
rs247913232	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108058666	GCCTAATGCCCACAT[G/T]GCCACCATTTAGGTA	84585
rs247932105	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108072352	ACCCAAGCACAAGCT[C/T]ACACCACCCTTCTAA	84585
rs248075060	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	GRCm38.p3	9:108078163	CAACACGTCCAAAGT[A/G]AGGTGGCCTAGAATA	84585
rs248106206	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079733	GATGGATGCTCCTCG[A/G]ATGTGCTGCTAGGGG	84585
rs248108221	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108068315	TCGGTAGAGACGTAG[A/G]AGTGACATCATCAAC	84585
rs248134671	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108061959	TAGTGCCCAAGGCAG[A/G]ATAGGGGTGCGGCTC	84585
rs248232435	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108064569	CTGTACCCTCTTTCA[C/G]CCGACCCCCTGCAGA	84585
rs248236012	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108060690	AGATAGCAGAGAGAG[A/G]AGAGAGAGTGAGTGC	84585
rs248293419	in-del	-/TT			intron-variant	Rnf123	Mm_Celera	9:108064815	TTTTGTTTGTTTTGG[-/TT]TTTTTTGTTTTTTGT	84585
rs248737463	snp	C/T			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108069075	CCACTCAGAGCTCTC[C/T]GTCTCCACCAGCCGC	84585
rs248767633	snp	C/T			intron-variant, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055726	TCCCAGATGGATCCC[C/T]TTGTGTGCTCAGCTC	84585
rs248771950	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108066495	CTAGGATCCCAGGAG[A/G]GAAAGGCAGCAGAGG	84585
rs248931330	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108065282	CAGGTTGGCCTTGAA[C/T]TAATGGAGATCTTCC	84585
rs249260125	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108057140	CTCTTGCTGGGCAAG[C/T]CACAGGCTGCAGGTG	84585
rs249267409	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108062809	TCTGTGTGCACCAGC[A/G]CCCCCCAGGCAAGTG	84585
rs249421005	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108072928	TTGGAGGCCTAACTG[A/G]GCTACACAGAGAGGG	84585
rs249425109	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108061970	GCAGGATAGGGGTGC[A/G]GCTCTGCTTTCCAAA	84585
rs249488937	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108072118	GTGTGTAATTTCAGC[A/G]TGGGGAAGAAGAGAA	84585
rs249523924	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108064775	CACAGTGGGATGCTT[C/T]CGAGTTTTGTTGTTG	84585
rs249914146	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108076517	GTTACAGATGGTTGT[A/G]AGCCACTATGTGGTT	84585
rs249943548	snp	A/G			upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080933	AAATTCTCATGGAGT[A/G]GATGTGGTAGACCAG	84585
rs249953534	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108061720	AAACATGGAGGCTGA[A/C]AATGGGGCATGCTGG	84585
rs249980470	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108070350	AGATGGGTAAGGTTA[C/T]TAACCTAGTACCCTC	84585
rs249995930	snp	C/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108051991	GAAGGAGTGCTACCT[C/T]GTGCGTCCTAATTTG	84585
rs250040974	in-del	-/TTT			intron-variant	Rnf123	Mm_Celera	9:108074333	ATATAGCAAAATCAC[-/TTT]TTTTTTTTTTCTTTC	84585
rs250300251	in-del	-/T			intron-variant	Rnf123	Mm_Celera	9:108063174	CACTGCCACAGCCAG[-/T]TATTTTTCTCTTAAA	84585
rs250491242	in-del	-/T			intron-variant	Rnf123	Mm_Celera	9:108074771	CAAGCAAGGAGCCTC[-/T]AAAGTGTGCACAGTG	84585
rs250650275	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108068440	CCCATGATGAAGTCC[A/G]ACAGCCTGGCCTAAG	84585
rs250662076	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108059646	CCTACTCCCCAGATC[A/G]TGAATGGCCCCATCA	84585
rs250725033	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108067760	TATGTTTCCTTTGGT[G/T]TCTGCCTACTAGAAG	84585
rs250873526	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108061442	TAGAAGCGTCCAAGA[A/G]ACTCAAGAGGTGGCA	84585
rs250939109	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108077698	CATCCCCCCCCCCCC[A/C]GCCCCGGTCATGCCA	84585
rs250958281	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108072518	AGGCGGGAGACTAGG[C/T]GGAGACTAGGGAGGA	84585
rs250967136	in-del	-/GCAGA			intron-variant	Rnf123	Mm_Celera	9:108065108	CCTGACACTGGAGAT[-/GCAGA]GCATTGTGAGCTGCT	84585
rs251117027	snp	C/T			intron-variant, utr-variant-3-prime	Rnf123	Mm_Celera	9:108057929	TCCTCCACGAGCTTC[C/T]GCCAAGCTGGAGGGG	84585
rs251155316	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108065067	CGTGCATGCCCAATG[C/G]CACAGAGATCAGAAG	84585
rs251330088	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075451	AAAAATAAATACATT[A/G]TTTTTTAAAAAGAAT	84585
rs251330609	in-del	-/CTGTCCTAG			intron-variant, utr-variant-3-prime	Rnf123, Amigo3	Mm_Celera	9:108055657	GCAGCACTGTGCTGT[-/CTGTCCTAG]CTGACTGCTATGACA	84585
rs251610089	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108077393	AGGAGGGGAAAAGAT[A/G]CGGTACAGATAGTCG	84585
rs251610699	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, intron-variant	Rnf123, Mst1	GRCm38.p3	9:108078906	CAGGACTTATTGGAC[A/G]CAGTTAGTAAGACCT	84585
rs251661199	snp	C/T			intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054801	TGGCCGTGTGCAGCT[C/T]GCAGTAGCTGAAGAC	84585
rs251741412	snp	A/G			intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108053556	CTTGCCGGTAGCACT[A/G]CCTACCACTGCTGCA	84585
rs251748875	in-del	-/C			intron-variant	Rnf123	GRCm38.p3	9:108073812	TTTGCCAGACTCTTG[-/C]CTGTCCTTTCAGGGA	84585
rs252016812	snp	C/G			intron-variant	Rnf123	GRCm38.p3	9:108073543	ATAGATTCTGCAAAG[C/G]CCCCTCTTCACCCCT	84585
rs252206574	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108067336	CCCGGTGCCAGACGC[C/T]CTGGTATGCTGGGCA	84585
rs252249203	snp	A/G			synonymous-codon, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052085	AGAGATGGGGTGGGC[A/G]TAGCAGATTGGGCAG	84585
rs252336501	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108071550	GAACACTGGAGGATG[C/T]TTGGCTGAAGCTCCA	84585
rs252375861	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108061524	AGCCCAGCAGGCATG[A/G]GTAGAGCGATCAATG	84585
rs252427010	in-del	-/A			intron-variant, utr-variant-3-prime	Rnf123	Mm_Celera	9:108057875	GCTACAGCTGGGAGT[-/A]AGGAGGCAGGCAGAG	84585
rs252471486	in-del	-/C			intron-variant	Rnf123	Mm_Celera	9:108062809	CTGTGTGCACCAGCG[-/C]CCCCCCAGGCAAGTG	84585
rs252642981	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108074335	ATAGCAAAATCACTT[G/T]TTTTTTTTTTCTTTC	84585
rs252925567	snp	A/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	Rnf123, Mst1	Mm_Celera	9:108079066	ACCGAACCGACTAAG[A/T]CTGGGTGGCCAAGGA	84585
rs252951896	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108068763	GGCTCCTGACCCATA[A/C]TCTCTCTCTCTCTCT	84585
rs252951910	snp	C/T			upstream-variant-2KB	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108080089	AGCAGGCACCAGGGA[C/T]TCCATGCAACTTCTG	84585
rs253287006	snp	C/T			intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054690	GCTGAGCGCACAGTC[C/T]TCCATGCTTAGCACT	84585
rs253368134	in-del	-/A			intron-variant	Rnf123	GRCm38.p3	9:108075233	AGGAGGAAGAGGAGG[-/A]AGGGGGAGGGGGGGA	84585
rs253423759	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108063779	GGGGACGGGGCAGGG[G/T]GGGTCATGCCTCCAT	84585
rs253499620	snp	C/T			intron-variant, downstream-variant-500B, upstream-variant-2KB	Mst1, Mir7088, Rnf123	Mm_Celera	9:108081773	CTGTAGTAAGAATCT[C/T]TGTCTACAGGTATAC	84585
rs253555720	snp	C/T			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108069744	GATGGCTGGGAAGTA[C/T]GCCATTCCTAGGCCC	84585
rs253934418	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108063658	GGGCAGTGCCCCTCC[A/G]ATGGCCAGGGCTTGC	84585
rs253978310	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108077270	TGAGAATAGGACACC[A/G]TGCCCTCCTTCAGAA	84585
rs254047673	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108072460	TGCCCTTAGCTCGCA[A/G]CCTATCTTCTCTCAG	84585
rs254076659	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073580	CCCCAGGCTGAAGTC[A/G]GGAGCCAGCAATACC	84585
rs254077516	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108062494	TGCCCCAGCATCCCT[C/T]CCAGTATACCTAGGA	84585
rs254120667	in-del	-/TGCATGCG			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	Mm_Celera	9:108078323	TCTCATTAGTTTTCT[-/TGCATGCG]TGCACGCGCTCACAC	84585
rs254223704	in-del	-/AG			intron-variant, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055953	CTGAGACAAGGAAAC[-/AG]AGGTACCATGAGGCT	84585
rs254270079	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108069294	CTGGGTAGGTGCCAC[C/T]GAGTTAAGCCAGCAA	84585
rs254446062	snp	A/T			upstream-variant-2KB	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108079910	CTTGGCAACTCCTGT[A/T]TAGCAGAGTCTTTTG	84585
rs254467523	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108067467	CTTCCTCCACACGCA[A/G]GGGACTCTTAATATA	84585
rs254645985	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108066742	GCTGAGGATTCCGCA[C/T]CTTACCCTGCGCCCT	84585
rs254711880	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108076865	GGGTTCCAGTTATGA[A/G]CCACACCCTTCAGAT	84585
rs254809758	snp	C/T			intron-variant, upstream-variant-2KB	Rnf123, Amigo3	Mm_Celera	9:108052726	TACTTACCAACCCTC[C/T]CAGGTGTTTGGTCCC	84585
rs255041678	in-del	-/G			intron-variant	Rnf123	Mm_Celera	9:108067085	CCAAGGCCTGAGGCA[-/G]GGGGCTGACCTTCAA	84585
rs255054228	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108059860	AGGAGGCACAGAGGA[G/T]GCATTTACTGCGAGG	84585
rs255091579	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108060609	AGGCTGGGGACAGGG[C/T]AGATGATTTGTGAGC	84585
rs255191847	snp	C/T			intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108053496	CCCCGATATATGCAT[C/T]TGTGCTGCCGATGTG	84585
rs255218320	in-del	-/AAGGAAGG			intron-variant	Rnf123	Mm_Celera	9:108076110	AGAGGGAAAGAAGGA[-/AAGGAAGG]AAGGAAGGAAGGAAG	84585
rs255529938	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108074374	GGGTTTCTCTGTGTA[G/T]CCCTGGCTGTCCTGG	84585
rs255784468	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108071748	TGTGTCTAAAAAGAG[C/T]GACAGTGTACTCAAT	84585
rs255838417	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108076259	GAAGCAAGGGAGGGA[G/T]CGCTAGACATGGTTG	84585
rs255878875	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108071166	CCCCAGGAGGTCATC[A/G]TCCACAAGGAGAAGC	84585
rs255892763	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108066188	ACTGGGCAGAAGGCC[C/T]AGTAGCCCCCACAAC	84585
rs255914808	snp	C/G			intron-variant	Rnf123	GRCm38.p3	9:108061468	TGGCAGGTGAGTTAG[C/G]CAGGAGAGGTAGAAG	84585
rs256026411	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108070211	GGTTATGAGGTTGGC[C/T]CTCACCTTGCCATAA	84585
rs256384488	snp	C/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055158	CTGGCATCAGAGTCT[C/G]GGGACCACCCCCAGG	84585
rs256425381	snp	C/T			intron-variant, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055889	AAGCAGTTTACACAT[C/T]ACCAGTTACTCTTTG	84585
rs256550785	in-del	-/CAGGAC			intron-variant, upstream-variant-2KB, cds-indel, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108051611	GGGGACAGACATGGA[-/CAGGAC]CCTGCTGGGTGTAAC	84585
rs256568448	snp	G/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Rnf123, Mst1	Mm_Celera	9:108078509	CTGTCTCAGTGTAGG[G/T]GTGTGCTGCACCACA	84585
rs256661363	in-del	-/AG			upstream-variant-2KB, utr-variant-5-prime	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080393	AGGGGGTGTGGAGCC[-/AG]AGTCACCCAATCCTG	84585
rs256717005	in-del	-/CTCTTGTCTTTGGAGAGCAGGAGGC			intron-variant, utr-variant-3-prime	Rnf123, Amigo3	Mm_Celera	9:108055499	GTGACTAACCTGGGA[-/CTCTTGTCTTTGGAGAGCAGGAGGC]CTCTCAAGAGCTGGC	84585
rs256730533	snp	A/G			intron-variant, downstream-variant-500B, upstream-variant-2KB	Mst1, Mir7088, Rnf123	GRCm38.p3	9:108081725	ACTTCAGGTCAGACC[A/G]TTAGGCCTGAAGCAG	84585
rs256762208	in-del	-/A			utr-variant-5-prime, upstream-variant-2KB, intron-variant	Rnf123, Mst1	Mm_Celera	9:108079076	TAAGACTGGGTGGCC[-/A]AAGGATGTCAAGGGC	84585
rs256769394	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108070719	AGCCTCAGTGGGGTG[C/T]GCTCACCTTTGTACA	84585
rs256828168	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108077079	CTCTTATGTAAGGGT[C/T]AGGCAGAGGCTACAG	84585
rs257003757	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108066835	GCCGCAGACCCACAT[A/G]GGTGTCTTAGGTCAC	84585
rs257041510	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108057280	TGTTCCCACTAGTGT[C/T]AAGGCCAGCTTCATG	84585
rs257096904	snp	A/G			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108068166	CTTCTCGTGTCTCAG[A/G]ATGGACATAGTGAGG	84585
rs257178483	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108066007	GAATATCCTGTCTCC[C/T]ACTGACTCCTGGGGA	84585
rs257425489	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108070438	ATAGTCCATCCTCGG[G/T]GGGGGGCAGCCCGTA	84585
rs257730205	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108073431	TGGAAGGGTTATAAA[G/T]GTGCAGAGCACTGGC	84585
rs257761836	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108063216	TCCTGGGCCTTCCAG[A/G]AGGAGAGGGAATTCC	84585
rs257923829	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108065526	CAGTCTCTTGTGCCC[A/G]AGGAAGGCACTGCTG	84585
rs258080029	snp	A/C/T			intron-variant	Rnf123	GRCm38.p3	9:108075762	TAAGTTCCAGGACAG[A/C/T]CAGGGCCACACAGAG	84585
rs258145217	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108072409	CAACAAAGCAGCTGA[C/T]GTCAAGATGTGAAGA	84585
rs258183414	in-del	-/GTATC			intron-variant	Rnf123	Mm_Celera	9:108072483	CTCTCAGACGCATCT[-/GTATC]GATTCTGGGTGAGAA	84585
rs258204643	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108062058	TGGCTAAGCCCTTAG[A/G]CTGTACAAGTGAGGG	84585
rs258234982	snp	C/T			synonymous-codon, upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052283	TTCCACCTGGGCCAG[C/T]TCCTCAGCGCTGATA	84585
rs258321449	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108071551	AACACTGGAGGATGC[C/T]TGGCTGAAGCTCCAG	84585
rs258445682	snp	C/T			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055210	GTGGTATAGAAGAGT[C/T]AAGCATACCACACTT	84585
rs258779182	snp	A/T			intron-variant	Rnf123	Mm_Celera	9:108060398	GAAGGGCAGCCATAA[A/T]AAAGTCCCCGTTCCC	84585
rs258836655	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108067223	GAGAATGGGAGAGAG[C/T]GGGGGTTTCCTAGGA	84585
rs258862649	in-del	-/AGA			intron-variant	Rnf123	GRCm38.p3	9:108073068	AGAGGGAGAGGGAGG[-/AGA]GGGAAAGGGAGAGGG	84585
rs258878653	snp	C/T			intron-variant, downstream-variant-500B	Rnf123	Mm_Celera	9:108057517	CTTGCACCTCAATTC[C/T]GTCCTAGAGTCCAGG	84585
rs258938947	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108069573	TGCTTCTTGTGTACA[C/T]ACCACAACAGCTAGG	84585
rs259500575	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108068067	GCTTGACGAACACTG[C/T]CCTCTGCTGACGTTA	84585
rs259535881	snp	C/G			intron-variant, downstream-variant-500B	Rnf123	Mm_Celera	9:108057500	CCCCATGCCCTTCCC[C/G]ACTTGCACCTCAATT	84585
rs259626443	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108077217	AAACAGAGTCCAGAG[A/G]GCAGCTGCAGGCAGA	84585
rs259662545	snp	C/T			synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108077756	AGCATCTGAGGTCAG[C/T]CTATAGCTCTTTCGG	84585
rs259760778	snp	A/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080234	ACCTAACGTTTCCAC[A/G]CAGAACCCTCCTAAG	84585
rs259930876	snp	C/T			upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108079578	GAGGCCTGACCCACA[C/T]GCAGCCTGAAAGACC	84585
rs260017584	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108060050	CGCGAGAACCCATTA[C/T]GAAAGGTGAGGAGAC	84585
rs260100720	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108076739	cctctctctctctct[C/T]tctttctttctttct	84585
rs260124751	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108064306	CAGCTGACTGTTCGA[A/G]GTCACAGGCTGCAGA	84585
rs260161668	snp	C/T			intron-variant, utr-variant-3-prime	Rnf123, Amigo3	Mm_Celera	9:108054937	CTGCTGCTTGCCCTG[C/T]TTGCTGCTGCAGTCT	84585
rs260280583	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108051495	CATCCACTTTGCCAT[C/T]AGCAGGGTAGGACTC	84585
rs260470576	in-del	-/CTCTCACACA			intron-variant	Rnf123	GRCm38.p3	9:108075553	AGTCTCTCTCTCTCT[-/CTCTCACACA]CACATACACACACAC	84585
rs260565587	in-del	-/C			intron-variant	Rnf123	Mm_Celera	9:108060516	CCAGTCTGCACTTGA[-/C]CCCCAGGACCTGAGA	84585
rs260603307	snp	G/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052191	ACAGATTAGTAAAAC[G/T]GCCTCTGTTATGCCA	84585
rs260779928	in-del	-/AG			intron-variant	Rnf123	Mm_Celera	9:108076209	GATAAAGAGAAAGAA[-/AG]AGAGAGAGAGAGAAA	84585
rs260830231	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108075789	AGAGAAACCCTGTCT[C/T]GAAACACCTCCCCCC	84585
rs260955625	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108075699	CACACCTTTAGCTCC[A/G]GCACTAGGGAGGCAG	84585
rs260958096	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108074824	GGCCCTAAAAGATAA[C/T]CACTAAAATCAATTC	84585
rs261324327	in-del	-/G			intron-variant	Rnf123	Mm_Celera	9:108074371	ACAGGGTTTCTCTGT[-/G]TAGCCCTGGCTGTCC	84585
rs261476874	snp	A/G			upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080774	AACCCAGAAGGCAGG[A/G]CTCCTAAGCCCGATG	84585
rs261562627	snp	A/G			intron-variant, missense	Rnf123, Amigo3	GRCm38.p3	9:108054247	GAAGAGCAGCTGCAC[A/G]CGCAGGTGGGCCAGT	84585
rs261592737	in-del	-/C			intron-variant	Rnf123	Mm_Celera	9:108077699	TCCCCCCCCCCCCCG[-/C]CCCCGGTCATGCCAG	84585
rs261677382	in-del	-/AAAAG			intron-variant	Rnf123	Mm_Celera	9:108072079	TTAAAAAAAAAAAAA[-/AAAAG]GGTGGACGTGATGGC	84585
rs261694571	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108077633	ATGTTCCATGGACCT[A/G]GGCCCTGGCTGCATC	84585
rs261769394	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108074954	TGGTCCACATAGTAA[G/T]TTCCAAGATAGCCAG	84585
rs261822351	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108070022	AGCCCACGCCTGTCA[C/T]GAAAGGAAGCCTTAC	84585
rs261913502	snp	C/T			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108080191	AGTCTGGGGATTGCA[C/T]AGAGTAGACGGGCTC	84585
rs262074741	in-del	-/A			intron-variant	Rnf123	Mm_Celera	9:108066771	CTGCCACAGGAACAT[-/A]AACCCGCCCTGCTAT	84585
rs262279708	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108068876	GTCTGCAGGCTGTGG[C/T]TACACAGAACCCTGG	84585
rs262413448	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108071525	GTAAGTCCCTGTCAC[C/T]CTTCTCCTTGAACAC	84585
rs262442456	in-del	-/CACACACACACACA			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	Mm_Celera	9:108078340	ATGCGTGCACGCGCT[-/CACACACACACACA]CACACACACACACAC	84585
rs262482432	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108076569	TTTCGGAAGAGCAGT[A/C]TCACCAGCCCCCTTG	84585
rs262504440	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108066581	GCTGCAGCCCTGCAA[A/C]CCAGCCAGGAGCCCA	84585
rs262897639	snp	C/G			intron-variant	Rnf123	GRCm38.p3	9:108073631	GACGGCTGAAGGCAA[C/G]CCTCTCTCTGAATAC	84585
rs262916858	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108063749	TATGTAGAACTCTCT[C/T]GATGCACAGGGTTGG	84585
rs262970575	in-del	-/TGCT			intron-variant	Rnf123	Mm_Celera	9:108062234	TGGGAGAGCCAGCCC[-/TGCT]TCCTGCTGACTCAGT	84585
rs263062639	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108059384	TGTGACAGTACCAGA[A/G]TAGCAGAGTGAGGAG	84585
rs263081658	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108076268	GAGGGAGCGCTAGAC[A/C]TGGTTGCACTATAAT	84585
rs263155853	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108061429	GGTGAAAGAAAGTTA[A/G]AAGCGTCCAAGAAAC	84585
rs263245526	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108070939	GAGCTTCTGGGACAG[A/G]CATGATGGGACTCTG	84585
rs263380495	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108067948	TCACAGTGAAGAATA[C/G]CCCTATTTGGGCAGC	84585
rs263477529	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108060673	GGGAGGGGAGGAAGC[C/T]AAGATAGCAGAGAGA	84585
rs263514782	snp	A/G			intron-variant, utr-variant-5-prime	Rnf123, Amigo3	GRCm38.p3	9:108053235	AGAGCAGGAGAAGCC[A/G]GCTGGGCAGGGGGAG	84585
rs263641810	in-del	-/TCTC			intron-variant	Rnf123	GRCm38.p3	9:108075540	TTATTATTTCATAAG[-/TCTC]TCTCTCTCTCTCTCA	84585
rs263645767	snp	C/T			intron-variant, utr-variant-3-prime	Rnf123, Amigo3	GRCm38.p3	9:108055690	TTGTAATAAAAGTGG[C/T]ACATGATCATCGCTG	84585
rs263695510	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108065232	TAAGGGTCTCACTAT[A/G]TAGTCCTGGCTGACC	84585
rs264163848	snp	A/T			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055311	GAGCCTTCCCTGTAC[A/T]GAAAGAGGACCCAGT	84585
rs264359560	snp	A/C			intron-variant	Rnf123	Mm_Celera	9:108060457	GATTAAGTGATGGGG[A/C]ACAGGACACAAGAAG	84585
rs264555733	in-del	-/GAGA			intron-variant	Rnf123	GRCm38.p3	9:108073238	TAGGAGAGGGAGAGG[-/GAGA]GAGAGCACTGACCTC	84585
rs264865165	snp	A/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108054977	ACCTGCTGGTGGGGC[A/G]TGCTGTGCCTGGTCC	84585
rs265031901	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	Mm_Celera	9:108077930	CTTGGGAGCAGGTAA[A/G]ACTGAACCATGCATA	84585
rs265036746	in-del	-/A			intron-variant	Rnf123	Mm_Celera	9:108072386	TAATCCTTTATCTGT[-/A]AACAAAACAACAAAG	84585
rs265041139	snp	C/T			intron-variant, synonymous-codon	Rnf123	Mm_Celera	9:108068106	TACATGGCAGATCTG[C/T]CTGGCAACAGGATAC	84585
rs265127623	snp	C/T			upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108081037	AGGGACTTGCTGGGC[C/T]CTTGAAAATATACAT	84585
rs265179127	in-del	-/CACACACACACA			intron-variant, cds-indel	Rnf123	Mm_Celera	9:108078341	ATGCGTGCACGCGCT[-/CACACACACACA]CACACACACACACAC	84585
rs265212417	in-del	-/AA			intron-variant	Rnf123	Mm_Celera	9:108056752	AGTCAGAAGCCTTGC[-/AA]CACTGGGGAGCCTTG	84585
rs265293013	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108072274	GACAACTTTTCTCTC[C/T]GGCCTCCACTTGCAC	84585
rs265348032	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108064662	CTTCCAAAGCTGTCC[A/G]TGGATGGTTTGCACC	84585
rs265365178	snp	A/C			intron-variant	Rnf123	GRCm38.p3	9:108074564	CACACCAGAAGAAGG[A/C]ATTGGATCTCATTAC	84585
rs265419133	snp	C/G			intron-variant	Rnf123	Mm_Celera	9:108066957	CTTAGGCTCCCAGGA[C/G]AGGTAGCAGGCAGAA	84585
rs265673899	snp	G/T			intron-variant	Rnf123	Mm_Celera	9:108068954	ACACAGACACACCTG[G/T]CATGGCCCCCTCTGC	84585
rs265683858	in-del	-/T			intron-variant	Rnf123	Mm_Celera	9:108064794	TTTTGTTGTTGCTAA[-/T]TTTTTTTTTGTTTGT	84585
rs265684081	snp	A/G			intron-variant	Rnf123	Mm_Celera	9:108059952	ACTGAGACCTGGATT[A/G]CAGGAAGTGTGAGCA	84585
rs265887082	snp	G/T			intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054075	CTACCACCTGCTCCG[G/T]CGCTGGCACCAGCGG	84585
rs265982035	snp	A/T			intron-variant, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055933	AACTAGACTCTGAAG[A/T]TCATTCTGAGACAAG	84585
rs265991034	in-del	-/GAG			intron-variant	Rnf123	Mm_Celera	9:108076975	TAACTAACAACAAAA[-/GAG]GAGGTTTGCTTTGCT	84585
rs266052121	snp	C/T			intron-variant	Rnf123	Mm_Celera	9:108058744	TCTGGGACAGGCCAT[C/T]CCACCCCCATTCCCA	84585
rs266146074	snp	A/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079848	AGTCCTCACTTTACA[A/G]GAAGAAACTGAGGCC	84585
rs387070942	in-del	-/A			intron-variant	Rnf123	Mm_Celera	9:108072906	GAGGCAGGAAAAAAA[-/A]TGTGAGTTGGAGGCC	84585
rs387320403	in-del	-/GAGA			intron-variant	Rnf123	GRCm38.p3	9:108076072	AGAGAGAGAGAGAGA[-/GAGA]AAGAGAGAGAGAGAG	84585
rs387487175	in-del	-/GAAGGAAG			intron-variant	Rnf123	GRCm38.p3	9:108076145	AAGGAAGGAAGGAAG[-/GAAGGAAG]AAAGAAAGAGAGCAA	84585
rs578267112	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108065862	CTAGCCCAGGCCTCC[G/T]TGGCTCTCCCACTCC	84585
rs578320772	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076052	AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGAGA	84585
rs578632297	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	GRCm38.p3	9:108078308	TTTTCTTATTTTCAG[C/T]CTCATTAGTTTTCTT	84585
rs578639614	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108074994	GTGAGATCCTACCTC[A/G]AAGAAGAAGAAGAAG	84585
rs578848154	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076098	AGAGAGAGAGAAAGA[A/G]GGAAAGAAGGAAAGG	84585
rs578875778	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073173	GAGGAGAGGGACAGG[A/G]AGAGGAAGAGGGAGA	84585
rs578903827	snp	A/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108080079	TCTACAGTAAAGCAG[A/G]CACCAGGGACTCCAT	84585
rs579103804	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076028	ACACACCAAGGAAGA[A/G]AGAGAGAGAGAGAGA	84585
rs579235705	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108064800	TTGTTGCTAATTTTT[G/T]TTTGTTTGTTTTGGT	84585
rs579415346	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076187	AAGAGAAAGAGAGAA[A/G]GAAGGAGATAAAGAG	84585
rs579913694	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108076660	TTTTTTCTTTTCCTT[C/T]CTTTCTTTCTTTCTT	84585
rs579959641	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075036	GAAGAAGGAGGAGGA[A/G]GAGGAGGAGGAGGAG	84585
rs580020024	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108066776	ACAGGAACATAAACC[C/T]GCCCTGCTATCTGGG	84585
rs580053261	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108052138	ACAGGGCAGAGTGGA[A/G]GAGTTGGGCTGGGAT	84585
rs580173724	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108072371	CCACCCTTCTAAATC[C/T]TAATCCTTTATCTGT	84585
rs580480738	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076153	AAGGAAGGAAGGAAG[A/G]AAGAAAGAGAGCAAG	84585
rs580633518	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108077670	TTCCTTCTCCTTCCC[C/T]CAACCCAAAGCACAT	84585
rs580674349	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075134	AGAAGAGGAGGAGGA[A/G]GAGGAAGAGGAGGAG	84585
rs580768328	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075166	AGGAAGAGGAGGAGG[A/G]GGAGGGGGGGAGGAG	84585
rs580890647	snp	G/T			intron-variant, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108056011	CACACCCAGTTCCCA[G/T]GAGGCCAGCAGTCCC	84585
rs581194761	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073038	AGAGGGAGGGGGAGA[A/G]GGAGGGGGAGGGAAG	84585
rs581198040	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075214	GGAGGAGGAGGAAGA[A/G]GAGGAGGAGGAAGAG	84585
rs581311654	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073231	AGGGAGGTAGGAGAG[A/G]GAGAGGGAGAGAGAG	84585
rs581415722	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108076773	TTTCTTTCTTTCTTT[C/T]TTGAGACAGTGTCTT	84585
rs581576194	snp	A/T			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055047	TAACACTAGCTCAGG[A/T]CAAGGTCTCAGACTA	84585
rs581714792	snp	C/T			upstream-variant-2KB	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108080346	TAGCAACTGTCACCC[C/T]ATGTGTCAGTCAAGT	84585
rs581755517	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075259	GGGGAGGAGGAGGAA[A/G]AGGAGGGTAATTTCT	84585
rs581899888	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076076	AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGAGA	84585
rs581948530	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073875	CCTCAACCACTGATT[A/G]ATGGCCCTGCTTCCT	84585
rs581965961	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108074997	AGATCCTACCTCAAA[A/G]AAGAAGAAGAAGAAG	84585
rs582306924	snp	A/C			intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Rnf123, Mst1	GRCm38.p3	9:108078541	GGTAGTCAGGAGCCA[A/C]GAGTGGTTAAGTTTA	84585
rs582344901	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076128	GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA	84585
rs582728910	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108064836	TTGTTTTTTGTTTTT[C/T]TTCGAGACAGGGTTT	84585
rs582767546	snp	A/C			intron-variant	Rnf123	GRCm38.p3	9:108076165	AAGAAAGAAAGAGAG[A/C]AAGAGAAAGAGAAAG	84585
rs582856186	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	GRCm38.p3	9:108078367	ACACACACACACACA[C/T]CATATAACCGTCTAT	84585
rs583088201	snp	A/C/G			intron-variant	Rnf123	GRCm38.p3	9:108075137	AGAGGAGGAGGAGGA[A/C/G]GAAGAGGAGGAGGAG	84585
rs583121411	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075190	GGAGGAGGAGGAGGA[A/G]GAAGAGGAGGAGGAG	84585
rs583197977	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108076196	AGAGAAAGAAGGAGA[G/T]AAAGAGAAAGAAAGA	84585
rs583273674	snp	C/G			intron-variant	Rnf123	GRCm38.p3	9:108072477	CTATCTTCTCTCAGA[C/G]GCATCTGATTCTGGG	84585
rs583596876	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108066785	TAAACCCGCCCTGCT[A/G]TCTGGGCTCAGAGCC	84585
rs583677338	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108072378	TCTAAATCCTAATCC[C/T]TTATCTGTAACAAAA	84585
rs583699288	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075039	GAAGGAGGAGGAGGA[A/G]GAGGAGGAGGAGGAA	84585
rs583714372	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108076664	TTCTTTTCCTTTCTT[C/T]CTTTCTTTCTTTCTT	84585
rs583883694	snp	A/C			intron-variant, upstream-variant-2KB	Rnf123, Amigo3	GRCm38.p3	9:108052881	GCTCACATACACAGA[A/C]ATAAGTAAATCTAAG	84585
rs584194329	snp	A/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055102	ACAGAGTGACCAAAT[A/G]TCCCATTAACATTAC	84585
rs584209578	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076090	AAAGAGAGAGAGAGA[A/G]AGAAAGAGGGAAAGA	84585
rs584385807	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	GRCm38.p3	9:108078267	CCCAGAGTAAGAGAT[A/G]TCATACTTAGCCCAA	84585
rs584689457	snp	A/T			upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108079542	TAGGTCCACCTGTCT[A/T]AACTCCTACCTTGCC	84585
rs584761469	snp	G/T			intron-variant	Rnf123	GRCm38.p3	9:108073234	GAGGTAGGAGAGGGA[G/T]AGGGAGAGAGAGCAC	84585
rs584791337	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108073083	GGGGAAAGGGAGAGG[A/G]AGAGGGAGAGGAAGA	84585
rs584980496	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075217	GGAGGAGGAAGAGGA[A/G]GAGGAGGAAGAGGAG	84585
rs585109673	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108076867	GTTCCAGTTATGAGC[C/T]ACACCCTTCAGATCG	84585
rs585534937	snp	C/G			upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108080916	CCAACACACTGTCAC[C/G]CAAATTCTCATGGAG	84585
rs585641262	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108074754	CTCACACTATGTTTA[C/T]ACAAGCAAGGAGCCT	84585
rs585796886	snp	A/T			intron-variant	Rnf123	GRCm38.p3	9:108075005	CCTCAAAGAAGAAGA[A/T]GAAGAAGAAGAAGAA	84585
rs585832424	snp	C/G			intron-variant	Rnf123	GRCm38.p3	9:108066762	CCCTGCGCCCTGCCA[C/G]AGGAACATAAACCCG	84585
rs586154132	snp	A/G			intron-variant, utr-variant-3-prime	Rnf123, Amigo3	GRCm38.p3	9:108055664	CTGTGCTGTCTGACT[A/G]CTATGACATTTTGTA	84585
rs586172781	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076136	GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA	84585
rs586342062	snp	A/G			upstream-variant-2KB	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108080215	CGGGCTCTGCCTCAG[A/G]GACACCTAACGTTTC	84585
rs586354335	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075057	GGAGGAGGAGGAAGA[A/G]GAGGAGGAGGAAGAG	84585
rs586384573	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108065861	TCTAGCCCAGGCCTC[C/T]TTGGCTCTCCCACTC	84585
rs586431864	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108076178	AGCAAGAGAAAGAGA[A/G]AGAGAGAAAGAAGGA	84585
rs586538776	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108076553	GATTTGAACTCCGGA[C/T]TTTCGGAAGAGCAGT	84585
rs586743863	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075161	GGAGGAGGAAGAGGA[A/G]GAGGGGGAGGGGGGG	84585
rs586931549	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108072947	ACACAGAGAGGGAGA[A/G]GGGGAGGGAGGAAGG	84585
rs586966858	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075205	AGAAGAGGAGGAGGA[A/G]GAGGAAGAGGAGGAG	84585
rs587252693	snp	C/T			intron-variant	Rnf123	GRCm38.p3	9:108076691	TCTTTCTTTCTTCCT[C/T]CCTCCCTCCCTCCCT	84585
rs587477132	snp	A/C			intron-variant	Rnf123	GRCm38.p3	9:108072427	CAAGATGTGAAGATT[A/C]CAGGGAACAGCATGC	84585
rs587510697	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108075232	GGAGGAGGAAGAGGA[A/G]GAGGGGGAGGGGGGG	84585
rs587564793	snp	A/G			intron-variant	Rnf123	GRCm38.p3	9:108077309	TCCAGCATCTGGTCA[A/G]GCCTAACAGAGAGGA	84585
rs864271006	snp	C/T			intron-variant, missense	Rnf123, Amigo3	GRCm38.p3	9:108053678	ATAAGCTGGAAGTCC[C/T]GGGCCATGGTGCGTT	84585