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

Hgs

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6280170	snp	A/G	0.485582	0.0836725	intron-variant	Hgs	GRCm38.p3	11:120479308	CAGGCGTAGGTGCCC[A/G]CCCTCCGGGGTCCCG	15239
rs6281276	snp	C/T	0.5	0	intron-variant	Hgs	Mm_Celera	11:120479500	GAACAGAGGCCCACA[C/T]CACCTAGGCTCTCAG	15239
rs13466219	snp	C/T	0.456747	0.140554	synonymous-codon, upstream-variant-2KB	Hgs, Mrpl12	GRCm38.p3	11:120483493	CCAGCTCATCTCCTT[C/T]GACTGACCTTGAGTC	15239
rs13466220	snp	A/T			missense, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469038	CAGCTTCTGTTGGAG[A/T]CAGACTGGGAGTCCA	15239
rs13466221	snp	A/G	0.244898	0.249948	utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483654	CTCTTCCCTGTCCTC[A/G]GTGGTCTGGCTCCTA	15239
rs26981053	snp	G/T	0.124444	0.216185	downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484027	GGTTGGACCAACAAT[G/T]TAATAGTCTGCATCT	15239
rs26981054	snp	C/T	0.124444	0.216185	utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483901	CAGCAAGGGTAGAAG[C/T]TTTAGGTATCTCTGT	15239
rs26981055	snp	C/T	0.231111	0.249285	utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483886	CATGTGGCTCCTGCA[C/T]AGCAAGGGTAGAAGC	15239
rs26981056	snp	C/G	0.124444	0.216185	utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483772	GCCCGGCTGTGTTGG[C/G]TGCCACAGGTGAATG	15239
rs26981057	snp	A/G	0.408163	0.193609	utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483688	CTGGTTCCCTGCTTC[A/G]GTCCTGATGCCGTCT	15239
rs26981058	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483336	AGCTTGTTCTAAGCC[A/G]AAGGTTTTGTTTGTG	15239
rs26981059	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483294	TGCCATATTGGTAAC[A/G]ACCTGATCTACTATG	15239
rs26981060	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483272	TACAAGAGATCACAC[A/G]TGCCATTGCCATATT	15239
rs26981061	snp	C/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483201	CAGACAGAATCATGA[C/G]ATGCCATTAAGTGCA	15239
rs26981062	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483139	GCCCTTGGACTTCTG[A/G]GCTTCCTTTGATCCC	15239
rs26981063	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483109	ACCAGCAGGTGAGCC[A/G]TCTCCCAGCGGCCTG	15239
rs26981064	snp	A/G	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120480803	TTCCTGCCAGTTAGT[A/G]TCGTCAGCCTCCCTC	15239
rs26981065	snp	A/G	0.408163	0.193609	intron-variant	Hgs	Mm_Celera	11:120480759	CACCTCAGGACTGCA[A/G]GTGTCTTGGCTCAGA	15239
rs26981066	snp	A/G	0.197531	0.244432	intron-variant	Hgs	Mm_Celera	11:120480750	CTTAGAAAGCACCTC[A/G]GGACTGCAGGTGTCT	15239
rs26981067	snp	C/T	0.489796	0.070696	intron-variant	Hgs	Mm_Celera	11:120480610	TCAATTTGTTTTGTC[C/T]GGTGGTTCTACTTCC	15239
rs26981068	snp	C/G	0.396694	0.202437	intron-variant	Hgs	Mm_Celera	11:120480560	GTGCCTATAGTGTGG[C/G]CTTGAACCATTGTAC	15239
rs26981069	snp	C/T	0.152778	0.230321	intron-variant	Hgs	Mm_Celera	11:120479035	GCTTCCTGAGCTTAA[C/T]GGGCATAGCGTTCAC	15239
rs26981070	snp	A/G	0.165289	0.235211	intron-variant	Hgs	Mm_Celera	11:120479006	ATCTACCTGCCTAGC[A/G]CCTTTGCGAGGATGC	15239
rs26981071	snp	C/T	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120478983	GAAGGACACAGTGGG[C/T]AGCGCCTATCTACCT	15239
rs26981072	snp	C/T	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120478905	AGTCATGCCCAGTCA[C/T]AGGTGGAAGAGGGCC	15239
rs26981073	snp	C/T	0.42	0.183303	intron-variant	Hgs	Mm_Celera	11:120478885	CAACTGCTGAGGTGC[C/T]TGCCAGTCATGCCCA	15239
rs26981074	snp	C/T	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120478637	CTCTCTTGACTGTCG[C/T]TCCTAGGGCAAGGTC	15239
rs26981075	snp	C/T	0.375	0.216506	intron-variant	Hgs	Mm_Celera	11:120478276	AAGATTGCTTGGGAT[C/T]ACTTGATCACTTGAT	15239
rs26981076	snp	G/T	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120478043	TAGATAGTCAAGTTA[G/T]TGTGGCCACTGCTGC	15239
rs26981077	snp	A/C/T	0.32	0.24	intron-variant	Hgs	Mm_Celera	11:120477902	GCCACAGATGGGACC[A/C/T]GGAGCTAGAAACAGC	15239
rs26981078	snp	C/T	0.277778	0.248452	intron-variant	Hgs	Mm_Celera	11:120477650	TGGCTGCTCATTTTC[C/T]AGGGATCACCACAGG	15239
rs26981079	snp	A/G	0.18	0.24	intron-variant	Hgs	Mm_Celera	11:120477001	GCTGGCTGAGGCACC[A/G]AGGTCCCTTCTGCCA	15239
rs26981080	snp	C/G	0.277778	0.248452	intron-variant	Hgs	Mm_Celera	11:120476868	ACACTGTCCTTTCTG[C/G]CACCTTCTGAAGGGA	15239
rs26981081	snp	C/T	0.42	0.183303	intron-variant	Hgs	Mm_Celera	11:120476104	TTCTCTTGGATTTCT[C/T]AACTGTGGTTTGTGT	15239
rs26981082	snp	G/T	0.18	0.24	intron-variant	Hgs	Mm_Celera	11:120475281	CGGACTCTGTGATGC[G/T]TCAGAACTGCAGGCC	15239
rs26981083	snp	C/T	0.165289	0.235211	intron-variant	Hgs	Mm_Celera	11:120475104	TTCACTGGGCCTGTC[C/T]TGCTCTGTCTCACAG	15239
rs26981084	snp	A/G	0.277778	0.248452	intron-variant	Hgs	Mm_Celera	11:120474682	ATAGCTTCCCATCTC[A/G]CTTCCCGCCTGACAG	15239
rs26981085	snp	C/T	0.375	0.216506	intron-variant	Hgs	Mm_Celera	11:120474437	CTAACCTGATGGTTT[C/T]GGAACCACATTCATC	15239
rs26981086	snp	C/T	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120474146	GCCATGTGGTTTAGG[C/T]CACAGAATTCGATGG	15239
rs26981087	snp	A/G	0.426035	0.177515	intron-variant	Hgs	Mm_Celera	11:120472941	GAAAAGCAGCCGTTA[A/G]CCCCAGGTCAAGTTG	15239
rs26981088	snp	C/T	0.396694	0.202437	synonymous-codon	Hgs	Mm_Celera	11:120472643	AAGTGATGCCATGTT[C/T]GCTGCTGAAAGAGTG	15239
rs26981089	snp	C/T	0.444444	0.157135	intron-variant	Hgs	Mm_Celera	11:120472513	TATCCTTTCCTAGTC[C/T]TGACAGTTTTGTCTG	15239
rs26981090	snp	G/T	0.345679	0.230967	intron-variant	Hgs	Mm_Celera	11:120472290	TGCAAGGCTACAAGA[G/T]TGGCTCATGCCAGCA	15239
rs26981091	snp	C/T	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120471820	TTGCACCTTACACAT[C/T]TACCCCACAGGGAGG	15239
rs26981092	snp	A/G	0.32	0.24	intron-variant	Hgs	Mm_Celera	11:120471783	AGAGCTCCGTAGAGA[A/G]AGGCCAGGCTCTGAC	15239
rs26981093	snp	A/G	0.132653	0.220748	intron-variant	Hgs	Mm_Celera	11:120471732	GGTCTTCCCTGAGTG[A/G]TTGGGAGTGAGGAGG	15239
rs26981094	snp	A/G	0.260355	0.249785	intron-variant	Hgs	Mm_Celera	11:120471712	GGGACAAGGGAGGGC[A/G]GACTGGTCTTCCCTG	15239
rs26981095	snp	G/T	0.336735	0.234472	intron-variant	Hgs	Mm_Celera	11:120471449	CACCTGGAGTCTCCT[G/T]AGCCCTCCCCACTTT	15239
rs26981096	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120471371	CTCCCCTACCTTTGC[A/G]CTAATCGTCTCTGCT	15239
rs26981097	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120471309	GCAAGCATAGACCCA[A/G]GAGAGTCGCTTCTGT	15239
rs26981098	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120471200	ATCCCCTGGAGAGAT[A/G]GAAGGAGGCATGGTT	15239
rs26981099	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120471131	GGTCCTGTCTTCCTC[A/G]TGCTTTTTGGAGAGT	15239
rs26981100	snp	A/G	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120471005	TCATCCCAACATAAT[A/G]TGTCACAGCCTCCCT	15239
rs26981101	snp	A/G/T	0.260355	0.249785	intron-variant	Hgs	Mm_Celera	11:120470925	TGCTCCTCTCCTGGA[A/G/T]GGAACCCTTAGAGGG	15239
rs26981102	snp	C/T	0.231111	0.249285	intron-variant	Hgs	Mm_Celera	11:120470900	TGCTGCAAGGGGCAG[C/T]AGGCTGGCTTGCTCC	15239
rs26981103	snp	C/T	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120470705	CCCCATTTCATGGGA[C/T]CCAGCATCAGGGTTT	15239
rs26981104	snp	C/T	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120470648	ACCTAAGGATTGTGA[C/T]GTGGATGGTGATACA	15239
rs26981105	snp	C/T	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120470467	AGACATTCAGAGCAG[C/T]ACATTCAGGGATGGG	15239
rs26981106	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120470448	ATATGTGTGAGCTTG[A/G]GGAAGACATTCAGAG	15239
rs26981107	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120470213	CAGAATACAGCAGGA[A/G]GAGCAGTGGGTGTGT	15239
rs26981108	snp	A/C	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120470202	CTGTTTGTGGGCAGA[A/C]TACAGCAGGAAGAGC	15239
rs26981109	snp	C/G	0.152778	0.230321	intron-variant	Hgs	Mm_Celera	11:120469985	GCAAGAGGGGCTCTT[C/G]CCTCTTCCCTGAACA	15239
rs26981110	snp	C/G	0.142012	0.225474	intron-variant	Hgs	Mm_Celera	11:120469950	TAACAAGTTAGGTGG[C/G]TTCAGAGACCTGTCT	15239
rs26981111	snp	A/G	0.336735	0.234472	intron-variant	Hgs	Mm_Celera	11:120469944	GGTTTCTAACAAGTT[A/G]GGTGGGTTCAGAGAC	15239
rs26981112	snp	C/G	0.32	0.24	intron-variant	Hgs	Mm_Celera	11:120469911	GGGCCTGGAACCCGA[C/G]TTTGAGCTGCTGCTT	15239
rs26981113	snp	A/G	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120469909	CAGGGCCTGGAACCC[A/G]ACTTTGAGCTGCTGC	15239
rs26981114	snp	A/G	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120469805	GTGAGCTCGGCCACT[A/G]AGCCTGGCTGCTCTC	15239
rs26981115	snp	C/T	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120469781	AGACCTTTAGCACTT[C/T]GTACAGTTGTGAGCT	15239
rs26981116	snp	C/T	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120469692	TAACTAGAGCGCTGT[C/T]GCAGTTGTTTCTCTC	15239
rs26981117	snp	C/T	0.152778	0.230321	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469546	CCCATCCTTTTCTCT[C/T]TCTGCTGTTACTAAT	15239
rs26981118	snp	C/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469520	GCTTTCCTAACCATA[C/G]TGAGGGCTTTCCCAT	15239
rs26981119	snp	A/G	0.391111	0.206368	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469257	TTGAGGAGGTCTGTC[A/G]GGCTAAACTCATGGT	15239
rs26981120	snp	A/G/T	0.152778	0.230321	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469204	TGGGACAATTAAAAC[A/G/T]GCACAATTTGGAGAT	15239
rs26981121	snp	A/G	0.152778	0.230321	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469136	AAGATTAAATGGGCA[A/G]CATGAGTTTTTTGTT	15239
rs26981122	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468955	TGACTTTTGACGGGC[C/T]GGCTCGGAAACATAG	15239
rs26981123	snp	C/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468826	CTGATAGGGACTAAG[C/T]ATCATTTCCACATTA	15239
rs26981124	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468795	GAACTGAGTGAAGCC[A/G]AGCTTGAGCTGACAG	15239
rs26981125	snp	A/C	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468697	CATTTTAAAGTGCCC[A/C]GCAAGCTGTGACAAA	15239
rs26981126	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468677	TGAGAAGCAGCAGGG[C/T]ATGCCATTTTAAAGT	15239
rs26981127	snp	C/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468365	CTTGCTCCTTTTTGA[C/G]CTAAGGTTTTCAAAG	15239
rs26981128	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468320	CCTCAATAAATGTGT[C/T]CAGGAGCAGGCCCCA	15239
rs26981129	snp	C/T	0.165289	0.235211	upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120467634	GGCGTTGCGCGTGCG[C/T]GAGCAGAAAAAGAAA	15239
rs26981130	snp	A/G/T	0.426035	0.177515	upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	GRCm38.p3	11:120467592	AGCGCAAGTCTCGCC[A/G/T]TGGAGCAGGACTCGG	15239
rs26981131	snp	C/T	0.35503	0.226867	upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	Mm_Celera	11:120467481	AATGAGGCCCGCCTC[C/T]GCTTAGCTTTCATTG	15239
rs26981132	snp	A/C	0.277778	0.248452	upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	Mm_Celera	11:120467466	TCCGAGCTACCACGC[A/C]ATGAGGCCCGCCTCC	15239
rs26981133	snp	A/T	0.408163	0.193609	upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	Mm_Celera	11:120467435	ACATCCCTTCCTCGG[A/T]TAACGCGCTTGTACC	15239
rs26981134	snp	C/T	0.132653	0.220748	upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120467093	ACCCAACCTACTGAC[C/T]ACAGGCACCGCGGCT	15239
rs26981135	snp	C/T	0.260355	0.249785	upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466952	CGTCAACCATAGAGA[C/T]GGGCCTTGAGAGTGA	15239
rs26981136	snp	C/T	0.165289	0.235211	upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120465871	TCGCCACAAAGTTGT[C/T]CTACCCACAGCTGCA	15239
rs46890120	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471135	CTGTCTTCCTCATGC[C/T]TTTTGGAGAGTTTAG	15239
rs211711843	in-del	-/GAAAAGTT			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120482671	CTACCAGGTATGTGG[-/GAAAAGTT]GCACCCAGCATCTAC	15239
rs211731773	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120481001	AGTGCTGGGATTAAA[C/G]GCAGGCACCACATTC	15239
rs212196577	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120471077	TGAGCCCCTGGAGAA[A/G]CATCTGAAGAGGATA	15239
rs212261854	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120478810	GTAAGGAGGCTCCAG[A/G]CTCCAGCTGCTCTGT	15239
rs212327077	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120477684	CTGTTGATTCAGGAC[G/T]TCACTGTGGCGTATT	15239
rs212825440	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120476568	CTGGATGCTGTTATG[C/T]TCCCACCTTGGTGAT	15239
rs212886351	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120475694	ATGAAGTTTACAAGC[A/T]GAGAATAGTGGTGCA	15239
rs213171728	snp	G/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468503	CTTGGGATAGCTCAC[G/T]TTCGTAAGGGAGGGG	15239
rs213246372	snp	C/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120467099	CCTACTGACCACAGG[C/T]ACCGCGGCTTCCATT	15239
rs213318379	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120474451	TCGGAACCACATTCA[G/T]CTCAGAATTGTGTGG	15239
rs213441661	snp	C/G			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483127	TCCCAGCGGCCTGCC[C/G]TTGGACTTCTGAGCT	15239
rs213509712	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120473147	AGGGAGAGAAAGGGA[A/G]AGAGAGAAGAGAGGA	15239
rs213520007	snp	C/G/T			intron-variant	Hgs	Mm_Celera	11:120482264	TGTGGATAAGACCCT[C/G/T]GGCTCAGCCCCTTGC	15239
rs213793461	snp	A/C			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466802	GCACTGAGACCAGCG[A/C]AAGCGGTGTGCTGTG	15239
rs213862040	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120473746	AGAGGGTTTCTCTGT[G/T]TAGCCCTGGCTGTCC	15239
rs213946693	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120480806	CTGCCAGTTAGTGTC[A/G]TCAGCCTCCCTCTGC	15239
rs214000030	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120480224	CAGTTTACAGAAGAC[A/C]GTGAGAATATAAAGA	15239
rs214100704	in-del	-/A			intron-variant	Hgs	Mm_Celera	11:120481398	TCTCGGACAGGTTTT[-/A]TTTTTTTTTTTTTTT	15239
rs214183959	in-del	-/T			intron-variant	Hgs	Mm_Celera	11:120475854	ATACAAAGAGGCATG[-/T]TTTTTTTTTTTAAAG	15239
rs214194442	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120471697	GTAACATCAGTGATA[C/G]GGACAAGGGAGGGCG	15239
rs214372573	in-del	-/TGTGTA			intron-variant	Hgs	Mm_Celera	11:120481909	ACTGAGGACCGTGTG[-/TGTGTA]TGTGTGTGTGTGTGT	15239
rs214503147	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120472136	GGCAGTTGTGAGCCA[C/T]CGTTTGTGTGCTGGA	15239
rs214601475	in-del	-/AACT			utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483825	CCGGAGTCTGATGTG[-/AACT]AACTGTGTGGTGTCC	15239
rs214822407	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120470158	GGGAGTCACAAGAGA[A/C]GGTAGATTCAGGTAT	15239
rs214889798	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120477446	TCTAGGTGTGGCAGC[A/G]GGGGTATGTGGAGGC	15239
rs215039595	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	Mm_Celera	11:120467442	TTCCTCGGATAACGC[A/G]CTTGTACCTCCGAGC	15239
rs215371711	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120476656	TTGCAAGCCGGGCGT[A/G]GTGGCGCACACCTTT	15239
rs215427216	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468321	CTCAATAAATGTGTT[C/T]AGGAGCAGGCCCCAT	15239
rs215498599	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120475566	GCCCTGGGCCAGTCA[C/T]TGGCTTTGAGTTTTG	15239
rs215504892	snp	A/C			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466640	CTCCAAAGAAGCTTG[A/C]AGTATTAACTCACCA	15239
rs215562942	snp	C/T			upstream-variant-2KB, synonymous-codon	Hgs, Arl16	Mm_Celera	11:120465743	TACTGCGGTGATGTT[C/T]TGCTTGGCACAAGCA	15239
rs216065375	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120474655	CCACAGCCTGTGTGG[A/C]CAGCGGCCCCTATAG	15239
rs216091719	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120471641	CCAGGCTGAGAACAC[C/G]CTCTCTAGGAGCCAC	15239
rs216145108	snp	A/G			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484160	AGGCGGGTGAGGAAG[A/G]GTGCAAACGCGGGCT	15239
rs216156631	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120471089	GAAACATCTGAAGAG[G/T]ATATCACCCTGCCTC	15239
rs216187108	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120473651	CCACCCCCACCATCC[C/T]CCCAAAAAGAAAGGA	15239
rs216411683	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120481053	TATTTTCCTTATGTG[C/T]ATCTGTGCACCACAG	15239
rs216673311	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469256	CTTGAGGAGGTCTGT[C/T]AGGCTAAACTCATGG	15239
rs216829280	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120482248	GAGAGTGCTTGCCCA[A/G]TGTGGATAAGACCCT	15239
rs217098374	snp	A/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468171	CTCAGCCTCTTGCGC[A/T]CTGGTAGTGCCTGGG	15239
rs217162491	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120478868	CGGCCCTCCTTGTCC[C/T]TCAACTGCTGAGGTG	15239
rs217164177	snp	A/G			upstream-variant-2KB, synonymous-codon	Hgs, Arl16	Mm_Celera	11:120467384	GGCGTTTCACCAGCA[A/G]GGTCTTCCCGACCCC	15239
rs217228021	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120474549	GGGCAGGGCCCAGCT[A/T]CTCCTCGGGGATCTG	15239
rs217281154	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120473940	GGCAGAAGCAGAGGC[A/C]GGCAGAGCTCTGTGA	15239
rs217553158	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120472875	AGCTCACTGTAAAGC[A/T]CGTGAGTGTCATACA	15239
rs217605913	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120482045	TTCATTTCTATCATA[A/G]TGGTCTTTTCTGAAG	15239
rs217667081	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120471778	CTTGGAGAGCTCCGT[A/G]GAGAGAGGCCAGGCT	15239
rs217724604	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120480346	CCCCACCCCCCCCCC[C/T]CTCTCTCTCTCCCCC	15239
rs217724681	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471264	GGAGTCCCCTGATTT[C/T]TTGGGGGGGATTAAA	15239
rs218002465	in-del	-/GATCACTT			intron-variant	Hgs	Mm_Celera	11:120478273	TGAAAGATTGCTTGG[-/GATCACTT]GATCACTTGATCACT	15239
rs218105879	snp	A/T			synonymous-codon	Hgs	Mm_Celera	11:120477312	AAAGCGGGATGAGAC[A/T]GCCCTGCAGGAAGAG	15239
rs218109086	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120476615	GAATCCAGCCCCAAT[G/T]AAATGTTGTCCTTAT	15239
rs218443236	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120476970	AGCCAGGAGAGAGAC[C/T]CACTTACCTTCTGCA	15239
rs218499614	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120476208	TGGGCATGACCGCCA[A/G]TGCTGTGGTTAAAGC	15239
rs218714410	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120474745	CAGCACTGGGGTTCA[C/T]TGTACTTCCAGAATC	15239
rs218766721	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120474166	GAATTCGATGGTCTT[G/T]GCACAGGTAGTCACA	15239
rs218770006	snp	C/G			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484296	TTTGCTCTTTCCCTC[C/G]CCGCTAAGCGCCCGC	15239
rs218828425	snp	A/C			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483307	ACAACCTGATCTACT[A/C]TGTGCTAAGGTGAAG	15239
rs218882041	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120482697	TCTACACCCAGCCGT[C/T]GCCTGTTCCTCATCT	15239
rs218979818	snp	A/G			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484012	TCGGGCAGCAGGCTG[A/G]GTTGGACCAACAATT	15239
rs219496222	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120481198	AGTCTGCATCCTCTA[A/C]AAGAGCAAAAAATGC	15239
rs219552543	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120480626	GGTGGTTCTACTTCC[A/G]TATGCCACAGGCTAC	15239
rs219752795	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120478913	CCAGTCACAGGTGGA[A/T]GAGGGCCTTGCTCTG	15239
rs220260421	in-del	-/CTCTTGC			intron-variant	Hgs	Mm_Celera	11:120469980	TTCCAGCAAGAGGGG[-/CTCTTGC]CTCTTCCCTGAACAC	15239
rs220486742	snp	C/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468950	GTTCTTGACTTTTGA[C/G]GGGCCGGCTCGGAAA	15239
rs220768386	snp	A/C/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120469406	CTCTGTGATCCCAGC[A/C/G]CTTAGGAAGTGAAGA	15239
rs220948774	snp	A/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466865	GAGCTAAGCATCCAC[A/T]GCCAGTGACAACTGC	15239
rs221003324	snp	C/T			upstream-variant-2KB, missense	Hgs, Arl16	Mm_Celera	11:120466018	GGACGGAGGCTTTTT[C/T]AAGTTCTTCTGCAGA	15239
rs221165950	snp	A/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466898	AAGCCCTCTGCTCTC[A/G]CCACCAAGAAATGCA	15239
rs221513090	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	Mm_Celera	11:120467585	GTGTGTAAGCGCAAG[G/T]CTCGCCATGGAGCAG	15239
rs221941025	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120472463	AGGATGTTGTGGTGG[C/T]ACATGGTTGGGCTTG	15239
rs221999887	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468695	GCCATTTTAAAGTGC[C/T]CAGCAAGCTGTGACA	15239
rs222041959	snp	A/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120467796	CAGCTCCAAGTCAGC[A/T]CCCTCGCGCGCACCG	15239
rs222042076	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120475747	AGGCAGAAGCAGGTG[A/G]ATCTCTGAGTTCAAG	15239
rs222101187	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120475045	GTTTCCTGCGAGTCC[C/T]CACCTCTCTGCTCCA	15239
rs222225557	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120469701	CGCTGTTGCAGTTGT[G/T]TCTCTCCTCAGACTC	15239
rs222303356	snp	C/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120465882	TTGTTCTACCCACAG[C/G]TGCACCTCCCCGCTG	15239
rs222497850	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120471920	TGGGGGCAGCGCAGG[A/C]TGAGTGGACAGGGAA	15239
rs223074171	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120477963	CTTCCTAGATTGTGA[C/G]CAGGGCTCACACTAA	15239
rs223278063	snp	A/C			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469347	GCTCAACACACTATA[A/C]CCCAGGTGTGACAGC	15239
rs223283805	snp	C/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466842	TGGATGGCAGCACCG[C/G]CATGAGGGAGCTAAG	15239
rs223300472	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120470797	CTGAATCAGACCAGG[A/T]CCTGTTTGTTCTAGC	15239
rs223344527	snp	G/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120465912	GCAGACCCTATGGTC[G/T]TGGCTGTACTCAAGT	15239
rs223359729	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120478096	TTCTGGTGGCACATG[A/C]TAGTCTCATAACCCA	15239
rs223402358	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120473218	TGAGGGGAGAAGGGA[C/G]AGAGGGGGAGAGGAT	15239
rs223424722	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120477259	ACCCCTTCCCAGGGG[C/G]CCTTCTCACTCTACT	15239
rs223451562	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120472554	TGTCAGGGGTTAGAA[G/T]TGGTGACCAGGGAGG	15239
rs223477256	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120476588	ACCTTGGTGATAATG[A/G]ACTGAACCTCTGAAT	15239
rs223500144	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120475253	TGAACAAGTGAGTGT[G/T]CACATCTCTGTGCGG	15239
rs223728564	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120475956	GTTACAGATGGTTGT[G/T]AGCCACCATGTGGTT	15239
rs224190336	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120474102	TCTGTTTGGAGGAAG[G/T]TCTTCTCTTTGGAGC	15239
rs224251502	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473441	CACCGGACAGTGGTG[A/G]TGCATGCCTTTAATC	15239
rs224299723	in-del	-/TGTG			intron-variant	Hgs	Mm_Celera	11:120481914	GACCGTGTGTGTGTA[-/TGTG]TGTGTGTGTGTGTGT	15239
rs224328933	snp	A/G			synonymous-codon	Hgs	Mm_Celera	11:120482645	CTCCTACCAGCCCAC[A/G]CCAACCCCAGGCTAC	15239
rs224494984	in-del	-/GTT			intron-variant	Hgs	Mm_Celera	11:120480279	ATTTTTCTAGAGTTG[-/GTT]TTTTTTTTTCTTTCT	15239
rs224592874	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473460	ATGCCTTTAATCCCA[A/G]CACTTGGGAGGCAGA	15239
rs224638496	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120475327	GCTCTGTCAGGAGGG[C/T]TAAGGGGCAAACCAA	15239
rs224698194	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120472362	ACCGGCGGGTTTTAG[A/G]CCAGGCCAGGGAGGC	15239
rs224703961	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120474468	TCAGAATTGTGTGGT[A/G]GCTGGGGCCGGAGCT	15239
rs224746970	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120481881	CTTAGGGTGAATTTA[C/T]AGTCTGTAGGTTACT	15239
rs224817902	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120480920	CCGTAGCTCTAGCTG[C/T]CCTGGAACTCACTCT	15239
rs224906586	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471828	TACACATCTACCCCA[C/T]AGGGAGGCAGTAGGC	15239
rs225184816	in-del	-/T			intron-variant	Hgs	Mm_Celera	11:120478639	TCTTGACTGTCGTTC[-/T]CTAGGGCAAGGTCTA	15239
rs225451694	in-del	-/TTTTTTTTTT			intron-variant	Hgs	Mm_Celera	11:120481394	GCATTCTCGGACAGG[-/TTTTTTTTTT]TTTTTTTTTTTTTTT	15239
rs225553862	in-del	-/CTCCA			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484352	TCCGCCTAGTGAGCT[-/CTCCA]CTTGGGAGGACTCCA	15239
rs225812636	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120479407	TCCACAGCATGCTCA[C/T]GTGAGGTGGTCCCAT	15239
rs225879601	snp	A/G			synonymous-codon	Hgs	Mm_Celera	11:120478605	CAACAGCATGGCAGA[A/G]GTGAGAGGCTCCTTT	15239
rs226687913	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120482470	AAGGAGAAACCCAGG[A/C]GAGGGTGTTCTTTTC	15239
rs227215276	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120481308	TCTCACTATGTAACC[A/C]TGGCTAACCAGAAAC	15239
rs227479759	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120470858	GGAGCCCTCGCTGTT[G/T]TTGTTTTGGCACACT	15239
rs228166378	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468128	TTCCTTAAACCTTTC[A/G]AGCCCCTTGGGGAAT	15239
rs228346248	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468971	GGCTCGGAAACATAG[C/T]TCAATGGACCCTTTG	15239
rs228382830	snp	A/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468204	TTTGAGAAGACATGT[A/T]TTTCTCATTTTTGAA	15239
rs228658102	snp	G/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466948	CCAACGTCAACCATA[G/T]AGATGGGCCTTGAGA	15239
rs228715943	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120474362	CTCGAGTATTTGGTC[C/T]CATGCCCCTGCCATC	15239
rs228716179	snp	A/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466432	CTACAGATAGGACCA[A/T]CAAGAGGGATGTAAA	15239
rs228774838	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473516	CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC	15239
rs228821326	snp	G/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120467150	TGCAAGCCTCAAAGG[G/T]CATGCATGACCTGAG	15239
rs228930127	snp	A/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466190	CAGACAACTTTTTAA[A/G]TGGATTTAAATTTAT	15239
rs229158143	in-del	-/CTGAGACCTCAGACACCTGGAGTCTC			intron-variant	Hgs	Mm_Celera	11:120471421	AGATGGCCCTTCCCT[-/CTGAGACCTCAGACACCTGGAGTCTC]CTGAGCCCTCCCCAC	15239
rs229263229	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471990	ACACAGCAGCAGCCC[C/T]GGGCCTCGGCACCTT	15239
rs229318942	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120480699	CTGAGGTGGGCTCAG[C/T]GGGCTTTTCATCTGT	15239
rs229319067	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471461	CCTGAGCCCTCCCCA[C/T]TTTCTTCCTGCTCCA	15239
rs229377280	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120479468	CCAGCCCTAGGGCCA[A/G]CAGCTCTGCTCAAGG	15239
rs229548889	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120472842	CCTGACCCAAAAGAA[A/G]GGCAACGTGAAGGAT	15239
rs229723364	in-del	-/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469579	CTACCCCCCCGCCCC[-/T]TTTTTTCCCCCCTCT	15239
rs229905385	snp	A/C			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469207	GACAATTAAAACAGC[A/C]CAATTTGGAGATACT	15239
rs230010996	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120470945	CCCTTAGAGGGAAAC[A/G]CAAATCCCAGTGTAA	15239
rs230015436	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120475724	ACACCTTTGATCCAG[C/T]ACTTAAGAGGCAGAA	15239
rs230076755	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120474793	TTTTTTTTTTTTTTT[A/T]AAAGATTTATTTATT	15239
rs230132493	snp	A/G			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484335	GCACTCAAAGGAGGC[A/G]GTTCCGCCTAGTGAG	15239
rs230391924	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120473881	ACACAGCTTTAAAAC[C/T]AGGCTAGTTGCAATG	15239
rs230408517	in-del	-/GTCTTCCCTGA			intron-variant	Hgs	Mm_Celera	11:120471718	AGGGAGGGCGGACTG[-/GTCTTCCCTGA]GTGATTGGGAGTGAG	15239
rs230440863	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120473155	AAAGGGAGAGAGAGA[A/G]GAGAGGAGTAGAGAC	15239
rs230496600	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120482277	CTGGGCTCAGCCCCT[A/T]GCACTATGAAAACAA	15239
rs230698519	snp	G/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469149	CAACATGAGTTTTTT[G/T]TTTTTTTGTTTTTTT	15239
rs230755620	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120476563	CCTGCCTGGATGCTG[C/T]TATGTTCCCACCTTG	15239
rs230914458	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120477226	CAAGGTCCCTTCTAG[A/T]CCCAAGAACACCTTC	15239
rs231097045	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120480228	TTACAGAAGACCGTG[A/G]GAATATAAAGAATTT	15239
rs231150703	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120478953	TGCAGACCAGGCATG[C/T]CACGTGTCAAGCATG	15239
rs231195443	snp	A/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120467034	GGCTTCGGGTTCTCC[A/G]CACTCAGAAGTCTAG	15239
rs231457140	snp	A/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120467926	GGCCGCCCGGGCTGT[A/T]CACTGAGTCCTGGGG	15239
rs231688772	in-del	-/C			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469586	CCCGCCCCTTTTTTT[-/C]CCCCCTCTTCCAGAG	15239
rs231706305	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120473686	GTACATTTGTTTAGA[A/G]TTTTTTGTTTGTTTA	15239
rs231749342	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120472709	CTTTGGAGAGGAAGG[A/G]GAAGGGAGGACCTGG	15239
rs231786552	snp	A/C			synonymous-codon, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483089	CCCAGGGCAGCAGCC[A/C]CTGTACCAGCAGGTG	15239
rs231805383	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120481470	GATGGTTGTATCTCT[C/T]GGAACTATAGTTATA	15239
rs231979896	snp	A/C/G			intron-variant	Hgs	GRCm38.p3	11:120477515	GTTTCTTCTTCTGCC[A/C/G]CAGAGACAGAAAACA	15239
rs232167231	snp	A/G			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484166	GTGAGGAAGGGTGCA[A/G]ACGCGGGCTTTTGCA	15239
rs232215547	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483283	ACACGTGCCATTGCC[A/G]TATTGGTAACAACCT	15239
rs232339930	in-del	-/C			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468583	AATCATCCCTCATCT[-/C]TCTAGAGCTTGCTAA	15239
rs232341145	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120472043	TGTTTTAATGTGTAT[A/G]GATGCTTTGCCAGCA	15239
rs232399958	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120480801	GCTTCCTGCCAGTTA[A/G]TGTCGTCAGCCTCCC	15239
rs232405148	snp	G/T			synonymous-codon	Hgs	Mm_Celera	11:120477348	GCTACAGCTGGCTCT[G/T]GCCCTATCACAGTCA	15239
rs232477619	snp	C/G			upstream-variant-2KB, synonymous-codon	Hgs, Arl16	Mm_Celera	11:120466657	GTATTAACTCACCAA[C/G]AGCGAATGGCAGTTT	15239
rs232537222	snp	C/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120465857	CGTCAAAGTGGTGCT[C/T]GCCACAAAGTTGTTC	15239
rs232600047	in-del	-/TT			intron-variant	Hgs	Mm_Celera	11:120481903	AGGTTACTGAGGACC[-/TT]GTGTGTGTGTATGTG	15239
rs232904582	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120475435	TGGCCACACTCTAGG[A/G]CAGGGTGGGCATAGT	15239
rs233056632	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120478389	GGTAAGCAGCGGTCT[C/T]GGGTGCTGTCCTCCC	15239
rs233080824	in-del	-/TGTTTATTTT			intron-variant	Hgs	Mm_Celera	11:120474971	CTCTCCAGCCCCTTC[-/TGTTTATTTT]TGTTTATTTTTAATT	15239
rs233460160	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120482886	GACCTAGTCTTTGCT[A/G]GGCACAGAGGGCTAT	15239
rs233545212	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120470001	CCTCTTCCCTGAACA[C/T]GAGCTAGGCCTTTCT	15239
rs233707544	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120476339	TAGATCAAACTCTAG[A/G]AAAACCCTGGCCTGC	15239
rs234335220	in-del	-/TG			intron-variant	Hgs	Mm_Celera	11:120481915	GACCGTGTGTGTGTA[-/TG]TGTGTGTGTGTGTGT	15239
rs234536465	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120482109	TGTCTTTGTTGCTGT[G/T]GTCTCAGTTTTGAAA	15239
rs234640518	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468506	GGGATAGCTCACTTT[C/T]GTAAGGGAGGGGTGA	15239
rs234717566	in-del	-/TA			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484313	GCTAAGCGCCCGCCT[-/TA]TAGTGTGCACTCAAA	15239
rs234735375	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120472877	CTCACTGTAAAGCAC[G/T]TGAGTGTCATACACA	15239
rs234801519	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120472313	TGCCAGCAGAGAGGA[A/C]AACCGGAATGCTGTC	15239
rs235201625	snp	C/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466813	AGCGCAAGCGGTGTG[C/T]TGTGGTGAGCTTCTG	15239
rs235341695	snp	A/C			upstream-variant-2KB, synonymous-codon	Hgs, Arl16	GRCm38.p3	11:120467409	GACCCCAGCAGCTCC[A/C]AGCAGGAGACACATC	15239
rs235392802	snp	C/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466843	GGATGGCAGCACCGC[C/G]ATGAGGGAGCTAAGC	15239
rs235392836	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120474568	CTCGGGGATCTGAAC[A/G]TGGAAAGCTTAGGCT	15239
rs235442929	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120473978	GCCAGCCTAGTCTAC[A/C]CAGTAAGTTGCAGGA	15239
rs235710140	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120472137	GCAGTTGTGAGCCAC[C/T]GTTTGTGTGCTGGAA	15239
rs236022295	snp	A/C/G			intron-variant	Hgs	Mm_Celera	11:120474354	GAGACTCACTCGAGT[A/C/G]TTTGGTCTCATGCCC	15239
rs236086391	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120473465	TTTAATCCCAACACT[C/T]GGGAGGCAGAGGCAG	15239
rs236156913	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120482698	CTACACCCAGCCGTT[A/G]CCTGTTCCTCATCTT	15239
rs236368926	snp	A/C			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469349	TCAACACACTATAAC[A/C]CAGGTGTGACAGCAC	15239
rs236428087	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120476701	GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTTGA	15239
rs236555666	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120471084	CTGGAGAAACATCTG[A/G]AGAGGATATCACCCT	15239
rs236619309	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120470214	AGAATACAGCAGGAA[A/G]AGCAGTGGGTGTGTT	15239
rs236621070	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120478853	CTGCAGCCTCAGAGG[A/C]GGCCCTCCTTGTCCC	15239
rs236683466	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120477695	GGACTTCACTGTGGC[A/G]TATTGAGGACGCCAA	15239
rs236965027	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120474695	TCACTTCCCGCCTGA[C/T]AGTTGTGAATGTGGA	15239
rs236976195	snp	C/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120465893	ACAGCTGCACCTCCC[C/T]GCTGCAGACCCTATG	15239
rs237242887	in-del	-/TC			intron-variant	Hgs	Mm_Celera	11:120469864	CTCTTCTAGCTGTCA[-/TC]CATGTACCCCTGAGG	15239
rs237266596	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120478032	TGGCTCCGTCCTAGA[G/T]AGTCAAGTTAGTGTG	15239
rs237331099	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120477254	TTCTCACCCCTTCCC[A/G]GGGGCCCTTCTCACT	15239
rs237587503	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120473020	CAACAAGTATGATTC[A/G]GGGTAGAACGAACTC	15239
rs237646179	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120482249	AGAGTGCTTGCCCAA[C/T]GTGGATAAGACCCTG	15239
rs237700827	in-del	-/CAATT			intron-variant	Hgs	Mm_Celera	11:120481834	GAGGCAGGAGGACTC[-/CAATT]CAAGGCCTAACAGAC	15239
rs237954075	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120472496	TCTCAGAGAACTCTG[A/G]GTATCCTTTCCTAGT	15239
rs238016575	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120481210	CTAAAAGAGCAAAAA[A/G]TGCTGTTAACTACTG	15239
rs238076567	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120480635	ACTTCCGTATGCCAC[A/G]GGCTACATCTTTTGT	15239
rs238109997	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120471642	CAGGCTGAGAACACG[A/C]TCTCTAGGAGCCACA	15239
rs238171138	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120479760	ATGTGGGTAGGGGAG[G/T]CCCAGGCTAGCCTGA	15239
rs238209238	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120470159	GGAGTCACAAGAGAA[A/G]GTAGATTCAGGTATA	15239
rs238390630	in-del	-/CG			intron-variant	Hgs	Mm_Celera	11:120481086	GAGCTGGGCTTTGCC[-/CG]CAGAGGCCAGAAGAG	15239
rs238429773	in-del	-/A			intron-variant	Hgs	Mm_Celera	11:120480219	CTTGCCAGTTTACAG[-/A]AGACCGTGAGAATAT	15239
rs238542362	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120482685	GGGCACCCAGCATCT[A/G]CACCCAGCCGTTGCC	15239
rs238604536	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120481615	ATTATCGGTGTAATC[C/T]ACGTGAGTGCTGATT	15239
rs238822082	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120475771	GTTCAAGGCCAGCCT[A/G]GTCTACAAAGCCAGT	15239
rs238937274	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120475572	GGCCAGTCACTGGCT[C/T]TGAGTTTTGTTTAGA	15239
rs239441115	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483203	GACAGAATCATGACA[C/T]GCCATTAAGTGCACG	15239
rs239529360	in-del	-/T			intron-variant	Hgs	Mm_Celera	11:120480443	CCAGGAGCCACTGGG[-/T]CACAGCAGGTTCTCA	15239
rs239683214	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120472419	GCCCTAGAGAGCTGG[A/T]GGAGTTTAAAGAAAG	15239
rs239762859	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120481128	CCTTGAAACTTGGAG[A/T]TTCAAGATGATTGTG	15239
rs240000241	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120481038	CAACTTTATTTTATA[G/T]ATTTTCCTTATGTGT	15239
rs240122795	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468766	AGTAGTACCTCTCTC[C/T]AGAGGGTCTGTGGGA	15239
rs240204174	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120467851	CAGGAGAGCGGGCCG[A/G]CCACCTAGACCGGCC	15239
rs240358756	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471097	TGAAGAGGATATCAC[C/T]CTGCCTCTCTCAGAT	15239
rs240646045	in-del	-/G			intron-variant	Hgs	Mm_Celera	11:120477789	CAGGCCTGGTCCTCT[-/G]GGTGCCCACGTCATC	15239
rs240946112	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120469716	TTCTCTCCTCAGACT[C/T]CAAGAATCCTTACCC	15239
rs241187783	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120476621	AGCCCCAATTAAATG[C/T]TGTCCTTATCAGAGT	15239
rs241302753	snp	A/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466925	TGCAGCTCTCTGGGG[A/G]CTCCAGGCCAACGTC	15239
rs241327895	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120471267	GTCCCCTGATTTTTT[G/T]GGGGGGATTAAAAGT	15239
rs241380724	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120470814	CTGTTTGTTCTAGCA[A/G]GTCCTAGCTGTAAAA	15239
rs241417410	in-del	-/TT			intron-variant	Hgs	Mm_Celera	11:120481395	GCATTCTCGGACAGG[-/TT]TTTTTTTTTTTTTTT	15239
rs241446689	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120478247	CATTTGGTGCCATGT[G/T]GGTCCTTGTCTGAAA	15239
rs241899527	snp	C/G			upstream-variant-2KB, synonymous-codon	Hgs, Arl16	Mm_Celera	11:120466007	GAAGAGTATGAGGAC[C/G]GAGGCTTTTTCAAGT	15239
rs241946231	snp	A/G			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484017	CAGCAGGCTGGGTTG[A/G]ACCAACAATTTAATA	15239
rs241956903	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120473232	ACAGAGGGGGAGAGG[A/G]TAGGAGAGCAAGAGG	15239
rs242014249	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120472576	CCAGGGAGGCACCCA[A/G]TAGTGACTGTCACCT	15239
rs242583002	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120472865	TGAAGGATTTAGCTC[A/C]CTGTAAAGCACGTGA	15239
rs242638633	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120472195	TCAGTGAGCTGCTTA[C/G]GCACTGAGCTGTGTC	15239
rs242638964	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120481965	GTGTGAGAAGCAAAC[C/T]AGGTTCCCCCTAATG	15239
rs242696690	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120480985	CTGCCTCTGTCTCCC[A/G]AGTGCTGGGATTAAA	15239
rs242763250	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120480390	CCAGGGTGCCAGGCA[A/G]GTAAAATCCCTTTAC	15239
rs242957358	in-del	-/T			intron-variant	Hgs	Mm_Celera	11:120480280	TTTTTCTAGAGTTGG[-/T]TTTTTTTTTTCTTTC	15239
rs243093398	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120476973	CAGGAGAGAGACCCA[C/T]TTACCTTCTGCAGCT	15239
rs243158435	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120476284	TTATGCTTTATATAT[A/G]TGGCCCTCAGCCCTA	15239
rs243215708	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120475342	TTAAGGGGCAAACCA[A/G]TGCTGCTCTGCAGGC	15239
rs243282290	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120474469	CAGAATTGTGTGGTG[C/G]CTGGGGCCGGAGCTT	15239
rs243341091	in-del	-/AAAA			intron-variant	Hgs	GRCm38.p3	11:120473582	AACAAACAAACAAAC[-/AAAA]GAAACAAACAAAAAC	15239
rs243402545	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483177	GGGTGCATCAGGGGC[C/T]TTGCTCAGCAGACAG	15239
rs243508538	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120467972	CTCTTTGGGGGTCCG[C/T]GACGGACCTCTCTTC	15239
rs243520513	in-del	-/CGCAG			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484450	GAATTCAAGGGGCTA[-/CGCAG]TGAGTTCCGTAGGTA	15239
rs243590381	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120475302	ACTGCAGGCCGCACA[A/G]GCTCCTCAAGCTCTG	15239
rs243708107	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120476564	CTGCCTGGATGCTGT[C/T]ATGTTCCCACCTTGG	15239
rs243772053	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120475591	GTTTTGTTTAGATAG[A/G]CTCTTGCTTGGACTT	15239
rs244111350	in-del	-/T			intron-variant	Hgs	Mm_Celera	11:120473248	TAGGAGAGCAAGAGG[-/T]TTTTTTTTTGGAAGG	15239
rs244148472	in-del	-/C			intron-variant	Hgs	Mm_Celera	11:120478828	CAGCTGCTCTGTGGA[-/C]CCCAGTATTCTGCAG	15239
rs244166908	snp	A/G			upstream-variant-2KB, synonymous-codon	Hgs, Arl16	GRCm38.p3	11:120466085	CTGGGTGGGGTTAGA[A/G]GCATCCATCATGAAC	15239
rs244241197	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120473442	ACCGGACAGTGGTGG[C/T]GCATGCCTTTAATCC	15239
rs244354748	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120479409	CACAGCATGCTCACG[A/T]GAGGTGGTCCCATTG	15239
rs244411499	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120478656	TAGGGCAAGGTCTAA[C/T]GTAGGCCAGAGACCC	15239
rs244973203	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120471954	CTCACAAGTCAGGGT[G/T]GCGGATGCTAGGAGC	15239
rs244997585	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120471829	ACACATCTACCCCAC[A/T]GGGAGGCAGTAGGCT	15239
rs245077074	in-del	-/GGAGTACAT			intron-variant	Hgs	Mm_Celera	11:120473667	CCAAAAAGAAAGGAG[-/GGAGTACAT]GGAGTACATTTGTTT	15239
rs245086591	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120480602	AACTGCCCTCAATTT[A/G]TTTTGTCCGGTGGTT	15239
rs245446526	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483756	ACCTTCTCTGGAGAG[C/T]GCCCGGCTGTGTTGG	15239
rs245611418	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120470679	GCTGGATTGGGCAAA[G/T]CGATGCTGTTCCCCA	15239
rs245902411	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120477930	AGCCCTGGCACCTGC[G/T]GGTGGTGGAAACTCT	15239
rs246244644	snp	G/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466455	GATGTAAAGTGTTGG[G/T]CGTATTCAGGTATCA	15239
rs246301387	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120473647	CCACCCACCCCCACC[A/G]TCCCCCCAAAAAGAA	15239
rs246301529	snp	C/T			upstream-variant-2KB, missense	Hgs, Arl16	GRCm38.p3	11:120465733	CACTTATTTCTACTG[C/T]GGTGATGTTTTGCTT	15239
rs246354432	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120472894	GAGTGTCATACACAC[A/G]GTACTCAGTAAAGCA	15239
rs246755945	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120474375	TCTCATGCCCCTGCC[A/T]TCTTCACAAAGAGCA	15239
rs246842047	snp	A/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466872	GCATCCACAGCCAGT[A/G]ACAACTGCTCAAGCC	15239
rs246861747	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483503	TCCTTTGACTGACCT[C/T]GAGTCTGGCGCTCAC	15239
rs246916309	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120474103	CTGTTTGGAGGAAGG[C/T]CTTCTCTTTGGAGCA	15239
rs246980711	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469113	GTGAAGAGAACCACC[C/T]CTCTTCTAAGATTAA	15239
rs247318294	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120469958	TAGGTGGGTTCAGAG[A/G]CCTGTCTTCCAGCAA	15239
rs247378858	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120477268	CAGGGGCCCTTCTCA[C/T]TCTACTCTGTCTGTC	15239
rs247380680	snp	A/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469255	CCTTGAGGAGGTCTG[A/T]CAGGCTAAACTCATG	15239
rs247443067	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120476613	CTGAATCCAGCCCCA[A/G]TTAAATGTTGTCCTT	15239
rs247498138	in-del	-/CATAGGTTCACAT			intron-variant	Hgs	Mm_Celera	11:120481152	GATTGTGAACCACAA[-/CATAGGTTCACAT]CATAGGTTCTGGGGA	15239
rs247529103	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120481376	GAATTAAAGGTGTGC[A/G]ATAGCATTCTCGGAC	15239
rs247674353	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471316	TAGACCCAAGAGAGT[C/T]GCTTCTGTGATTAAG	15239
rs247747376	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120479326	CTCCGGGGTCCCGCT[A/C]ATGATTCCTGGGGCC	15239
rs247773446	in-del	-/CTC			intron-variant	Hgs	Mm_Celera	11:120480481	CCCAGTAAAGAAAAT[-/CTC]CTCAGGACTGTCAGC	15239
rs247777405	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	Mm_Celera	11:120467445	CTCGGATAACGCGCT[C/T]GTACCTCCGAGCTAC	15239
rs248108228	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120472002	CCCTGGGCCTCGGCA[C/T]CTTTTCTATTTTTAA	15239
rs248163299	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120479061	TTCACCCTGCTGTGG[C/T]GCTCAGCTACCCACT	15239
rs248165099	snp	A/G			synonymous-codon	Hgs	Mm_Celera	11:120471488	TCCACAGAGGCAAGT[A/G]GAAGTTAATGTTCGG	15239
rs248545335	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120477089	CCTGGAAGGATGGTG[C/T]CAGTGCATGGTTGCT	15239
rs248556811	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471748	TTGGGAGTGAGGAGG[C/T]GGTGTTCCCTAAACC	15239
rs248618324	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120480243	AGAATATAAAGAATT[A/T]CCCAAGTTTTCTAAG	15239
rs248644840	in-del	-/TGTTTTTTTG			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469148	GCAACATGAGTTTTT[-/TGTTTTTTTG]TTTTTTTTTAATCCA	15239
rs248867997	snp	A/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120467162	AGGGCATGCATGACC[A/T]GAGAGAGGCCGACAC	15239
rs249225963	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468169	ACCTCAGCCTCTTGC[A/G]CTCTGGTAGTGCCTG	15239
rs249244173	in-del	-/C			intron-variant	Hgs	Mm_Celera	11:120478636	CTCTCTTGACTGTCG[-/C]TTCCTAGGGCAAGGT	15239
rs249407629	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120473931	AATCTCAGAGGCAGA[A/G]GCAGAGGCCGGCAGA	15239
rs249426030	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120475046	TTTCCTGCGAGTCCT[C/T]ACCTCTCTGCTCCAC	15239
rs249477287	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120473189	CCGTGAGCACGTGGC[A/G]AGGGAGAGGGGAATG	15239
rs249540287	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120482357	TCCCATAGGACCTCA[C/T]CCCACCCCACCCCAC	15239
rs249619565	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120481294	TTTGTGAGACAGGAT[C/T]TCACTATGTAACCCT	15239
rs249761813	snp	C/T			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484293	AGTTTTGCTCTTTCC[C/T]TCCCCGCTAAGCGCC	15239
rs249912325	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120471390	ATCGTCTCTGCTCAG[A/G]GCAATTGGTCTTACT	15239
rs250188098	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120482482	AGGCGAGGGTGTTCT[C/T]TTCTAATCTCATTTC	15239
rs250505675	in-del	-/G			intron-variant	Hgs	Mm_Celera	11:120473047	CTCTGGCATTTACAC[-/G]GCGCTCTGGTACTGG	15239
rs250714376	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120476753	GAGTTCCAGGACAGC[C/T]AGGGTTATACAGAGA	15239
rs250977974	in-del	-/AGTAA			intron-variant	Hgs	Mm_Celera	11:120472901	ATACACACAGTACTC[-/AGTAA]AGCAAACGAACCAGC	15239
rs251112948	snp	A/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466784	TATGGAAAAAACCAC[A/G]ATGCACTGAGACCAG	15239
rs251190076	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120473734	TGTTTTCTTGATAGA[A/G]GGTTTCTCTGTTTAG	15239
rs251309037	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469310	AGTATTTGCCTAGCA[C/T]GTATTAAACCTTGAG	15239
rs251370768	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468794	GGAACTGAGTGAAGC[C/T]GAGCTTGAGCTGACA	15239
rs251723719	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120472057	TGGATGCTTTGCCAG[C/T]AGTATATGTTCATGG	15239
rs251798654	in-del	-/ATAA			intron-variant	Hgs	Mm_Celera	11:120480522	CCCACCTTTTCTCTT[-/ATAA]ATATGTCCTGTTCTG	15239
rs251821070	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120482255	CTTGCCCAATGTGGA[C/T]AAGACCCTGGGCTCA	15239
rs251909724	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120481179	TCATAGGTTCTGGGG[A/G]TCAAGTCTGCATCCT	15239
rs252234314	snp	C/G			utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483969	CAGTGAAAATAAAAT[C/G]TATTTCAAAACTCTC	15239
rs252294155	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120478407	GTGCTGTCCTCCCTG[C/T]TCCTCGGCCCGACCA	15239
rs252382943	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120472349	GTGTGAGACACACAC[C/T]GGCGGGTTTTAGGCC	15239
rs252434254	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471812	ACAAGGTCTTGCACC[C/T]TACACATCTACCCCA	15239
rs252452436	in-del	-/GTGGAGTGTGCTGGGTACTGGCTGAGAAACC			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484046	TAGTCTGCATCTGTT[lengthTooLong]GTGGACTTGCCAACA	15239
rs252894359	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120476450	TGTGTCACTGTGGGT[A/G]TGGGCTTTGAGACCC	15239
rs252909985	snp	A/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466213	AAATTTATGATGCAG[A/G]AGTTTGAACCTAGGG	15239
rs253051570	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120474640	ACTTATTTCTAGGGT[C/G]CACAGCCTGTGTGGC	15239
rs253204532	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468524	AAGGGAGGGGTGATC[C/T]GAGTGTGAAGAGGTG	15239
rs253261059	snp	A/C			upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120467605	CCATGGAGCAGGACT[A/C]GGGGCGGCGCGGAGG	15239
rs253261150	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120475743	TAAGAGGCAGAAGCA[A/G]GTGGATCTCTGAGTT	15239
rs253318401	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120474826	ATATAAGTACACTGT[A/T]GCTGTCTTTAGACAT	15239
rs253505064	snp	A/C			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466859	ATGAGGGAGCTAAGC[A/C]TCCACAGCCAGTGAC	15239
rs253632113	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120482157	AGAAATTATCAGTGT[C/T]AGCTCTCCCTAACTC	15239
rs253902203	in-del	-/T			intron-variant	Hgs	Mm_Celera	11:120471135	CTGTCTTCCTCATGC[-/T]TTTTGGAGAGTTTAG	15239
rs254137118	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120479478	GGCCAACAGCTCTGC[C/T]CAAGGAGAACAGAGG	15239
rs254303870	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120470962	AAATCCCAGTGTAAA[A/G]GCCCTTGTATCCCTT	15239
rs254509945	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120477258	CACCCCTTCCCAGGG[G/T]CCCTTCTCACTCTAC	15239
rs254651727	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120471086	GGAGAAACATCTGAA[A/G]AGGATATCACCCTGC	15239
rs254714266	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120470345	ACACTTCTTTTGGGA[A/C]TGGGAAAGGCTTCCA	15239
rs254859225	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120476978	GAGAGACCCACTTAC[C/G]TTCTGCAGCTGGCTG	15239
rs255008668	snp	A/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469185	CCAGATTGTTTTGAT[A/T]TCTTGGGACAATTAA	15239
rs255315453	snp	C/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120465905	CCCCGCTGCAGACCC[C/T]ATGGTCTTGGCTGTA	15239
rs255617957	snp	C/G			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120482695	CATCTACACCCAGCC[C/G]TTGCCTGTTCCTCAT	15239
rs255685656	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120481850	CAAGGCCTAACAGAC[A/G]GTTAAGGCTTAGGTT	15239
rs255795633	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120474438	TAACCTGATGGTTTC[A/G]GAACCACATTCATCT	15239
rs256036970	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120471968	TGGCGGATGCTAGGA[C/G]CTCTGAACACAGCAG	15239
rs256096703	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120480648	ACAGGCTACATCTTT[A/T]GTCATTGTATCTCGT	15239
rs256151658	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120479454	GCTCCTTTCTGTCTC[C/T]AGCCCTAGGGCCAAC	15239
rs256482636	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120472711	TTGGAGAGGAAGGAG[A/G]AGGGAGGACCTGGGG	15239
rs256535973	in-del	-/TT			intron-variant	Hgs	Mm_Celera	11:120480279	TTTTTCTAGAGTTGG[-/TT]TTTTTTTTTTTCTTT	15239
rs256688445	snp	A/G			synonymous-codon	Hgs	Mm_Celera	11:120480041	CCAGGCTATGCCCAC[A/G]GCTGGGGGTGTACTC	15239
rs256961128	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468474	TTGTTGAATGAGTAA[C/T]AAGGGTGGTGTATCT	15239
rs257090566	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120476198	GGAGAGTAGTTGGGC[A/T]TGACCGCCAATGCTG	15239
rs257151772	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120475318	GCTCCTCAAGCTCTG[C/T]CAGGAGGGTTAAGGG	15239
rs257267980	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483829	AGTCTGATGTGAACT[A/G]ACTGTGTGGTGTCCA	15239
rs257283945	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120470138	TGAAGGTAGGCGGGC[A/G]TCCTGGGAGTCACAA	15239
rs257340635	in-del	-/T			intron-variant	Hgs	Mm_Celera	11:120480883	GCTATTGATTTTAGC[-/T]TTTTTTTGAGACAGG	15239
rs257354778	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120477428	CCCCTGCTGATGGAG[A/G]ACTCTAGGTGTGGCA	15239
rs257464417	snp	A/C			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120467914	GGCCTCGGGTGTGGC[A/C]GCCCGGGCTGTACAC	15239
rs257524930	snp	A/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120467018	TGCCCACCGGAAGAC[A/G]GGCTTCGGGTTCTCC	15239
rs257671786	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120472422	CTAGAGAGCTGGTGG[A/G]GTTTAAAGAAAGGGG	15239
rs257760719	in-del	-/CCCAGGTGTGACAGCACTGTCATAC			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469348	CTCAACACACTATAA[-/CCCAGGTGTGACAGCACTGTCATAC]CCCAGGTGTGACAGC	15239
rs258017652	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120475537	GGTGCTGTGGCTGCA[C/T]AGCAGCTGAGACTGC	15239
rs258086989	in-del	-/T			intron-variant	Hgs	Mm_Celera	11:120481339	TCATAGAGATCCACC[-/T]GCTTCTGCCTCCTGT	15239
rs258190940	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471101	GAGGATATCACCCTG[C/T]CTCTCTCAGATCATG	15239
rs258679565	in-del	-/TC			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469540	GCTTTCCCATCCTTT[-/TC]TCTCTCTCTGCTGTT	15239
rs258768976	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120471281	TGGGGGGGATTAAAA[A/G]TTGTGACCCTGAGCA	15239
rs258787328	snp	G/T			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120482924	AGGCCCTCTCCTCCT[G/T]GCTCTCGCTTCTGCT	15239
rs258788506	snp	A/C/G			intron-variant	Hgs	GRCm38.p3	11:120476631	AAATGTTGTCCTTAT[A/C/G]AGAGTTGCCTTGCAA	15239
rs258841103	in-del	-/TTTA			intron-variant	Hgs	Mm_Celera	11:120473713	TTTAGTTGGTTGATT[-/TTTA]TTTGTTTTCTTGATA	15239
rs258847099	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120470842	AAAGAGCTAAGTGTT[A/C]GGAGCCCTCGCTGTT	15239
rs259482188	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473357	GTGTGTTCTAGGCCA[A/G]CCTGGTCTAAATATG	15239
rs259514060	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120478867	GCGGCCCTCCTTGTC[C/T]CTCAACTGCTGAGGT	15239
rs259537833	snp	C/T			synonymous-codon	Hgs	Mm_Celera	11:120482618	CGGGCCCACCACCAG[C/T]CCTGCCTACTCCTCC	15239
rs259867296	snp	G/T			upstream-variant-2KB, missense	Hgs, Arl16	Mm_Celera	11:120466017	AGGACGGAGGCTTTT[G/T]CAAGTTCTTCTGCAG	15239
rs260018461	snp	C/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466940	GCTCCAGGCCAACGT[C/T]AACCATAGAGATGGG	15239
rs260058288	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120472017	CCTTTTCTATTTTTA[A/T]TTTTTATTTTTGTTT	15239
rs260076022	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120480535	TTATAAATATGTCCT[A/G]TTCTGCTTTGTGCCT	15239
rs260081711	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120474357	ACTCACTCGAGTATT[C/T]GGTCTCATGCCCCTG	15239
rs260083655	snp	C/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466290	CCCCAGATTGGCTTT[C/T]AAACAACAGGTTTTG	15239
rs260142980	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473483	GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCGA	15239
rs260488698	in-del	-/T			intron-variant	Hgs	Mm_Celera	11:120481128	CCTTGAAACTTGGAG[-/T]TTCAAGATGATTGTG	15239
rs260533532	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120477736	CCCCTGCCAGGGAGA[A/T]GAATCTCTTCCATAC	15239
rs260676999	snp	A/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466838	CTTCTGGATGGCAGC[A/T]CCGCCATGAGGGAGC	15239
rs260910716	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469585	CCCCGCCCCTTTTTT[C/T]CCCCCCTCTTCCAGA	15239
rs260961233	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468961	TTGACGGGCCGGCTC[A/G]GAAACATAGCTCAAT	15239
rs261010458	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120476318	TGTGGAGAAATCTCC[A/G]ACATATAGATCAAAC	15239
rs261063228	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120475390	CTTTGGGACAGGGTG[A/G]GCAGGGTGGACAGTG	15239
rs261676341	snp	C/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469391	AGGTGTGACAGCACT[C/G]TCTGTGATCCCAGCA	15239
rs262018584	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120474734	GGTCTGAGCAACAGC[A/C]CTGGGGTTCATTGTA	15239
rs262081643	snp	G/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468852	CATTATTTGCTTCTT[G/T]CATGGGAGGATGCCA	15239
rs262304882	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120473030	GATTCAGGGTAGAAC[G/T]AACTCTGGCATTTAC	15239
rs262368239	snp	C/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466886	TGACAACTGCTCAAG[C/T]CCTCTGCTCTCGCCA	15239
rs262471901	snp	A/C/T			intron-variant	Hgs	Mm_Celera	11:120472781	TTAATCTCAGCATTC[A/C/T]GGAAGAGGATTGCCA	15239
rs262611237	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120471682	TTCTAGCAACACTAG[A/G]TAACATCAGTGATAG	15239
rs262676528	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120470598	AGCAGAGGAGGAAAG[A/G]CTCTCTGGATCCATG	15239
rs262711343	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120477936	GGCACCTGCGGGTGG[A/T]GGAAACTCTTCCTTC	15239
rs262741945	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471370	TCTCCCCTACCTTTG[C/T]ACTAATCGTCTCTGC	15239
rs262771719	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120479354	GCCCTGGGACACCCA[C/T]GACTCTTTGCCTATA	15239
rs263016220	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120475788	TCTACAAAGCCAGTC[C/T]AGGACAGTCAGGGCT	15239
rs263040518	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120477110	CATGGTTGCTTACGG[C/T]GTCTCATTCTGTCTG	15239
rs263322565	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120474100	AGTCTGTTTGGAGGA[A/G]GGTCTTCTCTTTGGA	15239
rs263347365	in-del	-/C			intron-variant	Hgs	Mm_Celera	11:120481248	CTCTAGCCCCTGAGG[-/C]GTTTTTTTGTTTAAA	15239
rs263353882	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483237	GTACACATGCGTCCA[C/T]ATTGCACAGGAGACA	15239
rs263396494	snp	C/T			intron-variant, upstream-variant-2KB, missense	Hgs, Mrpl12	Mm_Celera	11:120482983	TCTGGTCACAGATAA[C/T]TCAGTGTCGGGCTCC	15239
rs263649320	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120481044	TATTTTATATATTTT[C/G]CTTATGTGTATCTGT	15239
rs263693933	in-del	-/AGTC			intron-variant	Hgs	Mm_Celera	11:120481745	TCTGTGGGGATGGAT[-/AGTC]AGTCATTAGAAGGCA	15239
rs263987151	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120478253	GTGCCATGTGGGTCC[C/T]TGTCTGAAAGATTGC	15239
rs264334707	snp	A/G			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484467	GAGTTCCGTAGGTAA[A/G]GGGGTGGGGGCGCCT	15239
rs264430737	in-del	-/TG			intron-variant	Hgs	GRCm38.p3	11:120473341	AGGCATGCTGATCTC[-/TG]TGTGTTCTAGGCCAA	15239
rs264467044	in-del	-/TTTTG			intron-variant	Hgs	Mm_Celera	11:120473065	GCTCTGGTACTGGCT[-/TTTTG]TTTTGTTTTGTTTTG	15239
rs264559052	snp	C/T			missense, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483422	CCTCCCCAGCAGCAA[C/T]CCCCTGTGGCCCAGC	15239
rs264946794	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468053	AGTCATGACTCAGAT[C/T]TTAGCTTCATGCGGG	15239
rs265089688	snp	A/G			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466168	CTGGTCATTTCACAA[A/G]AGCACACAGACAACT	15239
rs265106396	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120473446	GACAGTGGTGGTGCA[C/T]GCCTTTAATCCCAAC	15239
rs265248776	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120471890	GCTAATCAGGTTTCC[A/G]AGTGGCATGGTTCCT	15239
rs265301512	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120478418	CCTGCTCCTCGGCCC[A/G]ACCACACCAGTGCCG	15239
rs265447324	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120476545	AGCTCCTCCTGCACC[A/G]TGCCTGCCTGGATGC	15239
rs265590589	snp	A/C			intron-variant	Hgs	Mm_Celera	11:120474385	CTGCCATCTTCACAA[A/C]GAGCAGCGCTCCTTT	15239
rs265749381	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120481463	CAGAAGAGATGGTTG[G/T]ATCTCTTGGAACTAT	15239
rs265891008	snp	C/T			synonymous-codon	Hgs	Mm_Celera	11:120479149	GGCCCTGCAGAATGC[C/T]GTGAGCACTTTTGTC	15239
rs266232637	snp	A/G			synonymous-codon, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120482785	CCTCCCAGCCATCTC[A/G]CAGCCTCCACAGACC	15239
rs387106696	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120480827	CTCCCTCTGCCCTGT[C/T]GTCTGTGGCTGTGAG	15239
rs387249009	in-del	-/TG			intron-variant	Hgs	GRCm38.p3	11:120481953	GTGTGTGTGTGTGTG[-/TG]AGAAGCAAACTAGGT	15239
rs578607640	snp	A/C			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120467979	GGGGTCCGTGACGGA[A/C]CTCTCTTCCTCCGGG	15239
rs578618098	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120476758	CCAGGACAGCCAGGG[C/T]TATACAGAGAAACCC	15239
rs578721679	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473466	TTAATCCCAACACTT[A/G]GGAGGCAGAGGCAGG	15239
rs578983326	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120467795	TCAGCTCCAAGTCAG[C/T]TCCCTCGCGCGCACC	15239
rs579086662	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120481341	ATAGAGATCCACCTG[C/T]TTCTGCCTCCTGTAT	15239
rs579098016	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120473275	AAGGAAAGAAGGAAG[C/T]CAGCCAGCCAGGTGG	15239
rs579172887	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120473605	ACAAAAACAAACAAA[C/T]AAAAAAACTGAAAAG	15239
rs579219648	snp	C/G			intron-variant	Hgs	GRCm38.p3	11:120481203	GCATCCTCTAAAAGA[C/G]CAAAAAATGCTGTTA	15239
rs579271213	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120478956	AGACCAGGCATGTCA[C/T]GTGTCAAGCATGAAG	15239
rs579683411	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120480358	CCCTCTCTCTCTCTC[C/T]CCCTCCTCACTCTCT	15239
rs579702227	snp	G/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120469123	CCACCCCTCTTCTAA[G/T]ATTAAATGGGCAACA	15239
rs579761913	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120480323	AACACATGTTCTCCC[C/T]CCCTCCCCCCCACCC	15239
rs579771335	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120469574	AATTCCTACCCCCCC[A/G]CCCCTTTTTTTCCCC	15239
rs579887821	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120474433	TGCTCTAACCTGATG[A/G]TTTCGGAACCACATT	15239
rs579891596	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120481892	TTTACAGTCTGTAGG[C/T]TACTGAGGACCGTGT	15239
rs580262370	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120473614	AACAAACAAAAAAAC[C/T]GAAAAGAAAAACCAA	15239
rs580346144	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120482413	TTTACTTTTCTTTTA[C/T]GAGGATGTGAAACAT	15239
rs580386089	snp	G/T			intron-variant	Hgs	GRCm38.p3	11:120482110	GTCTTTGTTGCTGTG[G/T]TCTCAGTTTTGAAAC	15239
rs580537786	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120469133	TCTAAGATTAAATGG[A/G]CAACATGAGTTTTTT	15239
rs580592552	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120481151	TGATTGTGAACCACA[A/G]CATAGGTTCACATCA	15239
rs580886460	snp	A/C			intron-variant	Hgs	GRCm38.p3	11:120473031	ATTCAGGGTAGAACG[A/C]ACTCTGGCATTTACA	15239
rs580940504	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120476654	CCTTGCAAGCCGGGC[A/G]TGGTGGCGCACACCT	15239
rs580942180	snp	G/T			intron-variant	Hgs	GRCm38.p3	11:120473334	CAGACAGAGGCATGC[G/T]GATCTCTGTGTGTTC	15239
rs580999868	snp	G/T			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	GRCm38.p3	11:120482869	CAATATGCAGGTAAA[G/T]AGACCTAGTCTTTGC	15239
rs581059558	snp	G/T			intron-variant	Hgs	GRCm38.p3	11:120480677	GTGGTCACATCACTG[G/T]GGGTGGCTGAGGTGG	15239
rs581164985	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120476814	AAAAGAGTTGCCTTG[A/G]TCATGGTGTCTGTTC	15239
rs581440133	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	GRCm38.p3	11:120467597	AAGTCTCGCCATGGA[G/T]CAGGACTCGGGGCGG	15239
rs581530307	snp	G/T			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	GRCm38.p3	11:120483309	AACCTGATCTACTAT[G/T]TGCTAAGGTGAAGCT	15239
rs581572446	snp	G/T			intron-variant	Hgs	GRCm38.p3	11:120480448	AGCCACTGGGTCACA[G/T]CAGGTTCTCATCAGT	15239
rs581604611	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120476391	GTGTATATGCTTAGC[C/T]CAGGAAGTGGCACTA	15239
rs581720718	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120473117	AATTTATTTAGGGCA[C/T]GGGGAGGGGAGTAGA	15239
rs581813986	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120481914	GGACCGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT	15239
rs581874192	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473497	CAGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT	15239
rs582234305	snp	G/T			intron-variant	Hgs	GRCm38.p3	11:120481384	GGTGTGCGATAGCAT[G/T]CTCGGACAGGTTTTT	15239
rs582237695	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120468573	TGACATGGAGAAATC[A/G]TCCCTCATCTTCTAG	15239
rs582343396	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120478991	CAGTGGGCAGCGCCT[A/G]TCTACCTGCCTAGCA	15239
rs582432672	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120467809	GCTCCCTCGCGCGCA[C/T]CGGCCAGATGCTGCC	15239
rs582674664	snp	C/G			intron-variant	Hgs	GRCm38.p3	11:120481247	TTCTCTAGCCCCTGA[C/G]GGTTTTTTTGTTTAA	15239
rs582847799	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120469130	TCTTCTAAGATTAAA[C/T]GGGCAACATGAGTTT	15239
rs582944339	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120480360	CTCTCTCTCTCTCCC[C/T]CTCCTCACTCTCTTC	15239
rs582973185	snp	A/C			intron-variant	Hgs	GRCm38.p3	11:120473606	CAAAAACAAACAAAC[A/C]AAAAAACTGAAAAGA	15239
rs583070050	snp	G/T			intron-variant	Hgs	GRCm38.p3	11:120475840	AAAAAGCAAGTGTGA[G/T]ACAAAGAGGCATGTT	15239
rs583163354	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473775	CCTGGAACTTGCTCT[A/G]TAGACCAGGCTCACA	15239
rs583455381	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120469579	CTACCCCCCCGCCCC[C/T]TTTTTTCCCCCCTCT	15239
rs583558558	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120480327	CATGTTCTCCCTCCC[C/T]CCCCCCCACCCCCCC	15239
rs583576541	snp	G/T			intron-variant	Hgs	GRCm38.p3	11:120480456	GGTCACAGCAGGTTC[G/T]CATCAGTGCCCCAGT	15239
rs583760039	snp	A/C			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	GRCm38.p3	11:120482730	TCCCTCACCTCACTG[A/C]CTTCCTTCCATAGAG	15239
rs583764661	snp	C/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	GRCm38.p3	11:120467022	CACCGGAAGACGGGC[C/T]TCGGGTTCTCCACAC	15239
rs583841708	snp	G/T			intron-variant	Hgs	GRCm38.p3	11:120482265	GTGGATAAGACCCTG[G/T]GCTCAGCCCCTTGCA	15239
rs583950578	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	GRCm38.p3	11:120467464	CCTCCGAGCTACCAC[A/G]CAATGAGGCCCGCCT	15239
rs584043057	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120481158	GAACCACAACATAGG[C/T]TCACATCATAGGTTC	15239
rs584092270	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120476535	TAGAGCTCTCAGCTC[C/T]TCCTGCACCATGCCT	15239
rs584144281	snp	G/T			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	GRCm38.p3	11:120482871	ATATGCAGGTAAAGA[G/T]ACCTAGTCTTTGCTA	15239
rs584298908	snp	A/T			intron-variant	Hgs	GRCm38.p3	11:120476966	GCACAGCCAGGAGAG[A/T]GACCCACTTACCTTC	15239
rs584368556	snp	A/T			intron-variant	Hgs	GRCm38.p3	11:120473032	TTCAGGGTAGAACGA[A/T]CTCTGGCATTTACAC	15239
rs584608904	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120476664	CGGGCGTGGTGGCGC[A/G]CACCTTTAGTCCAGT	15239
rs584661084	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473414	AGAAAACCCTGTCTT[A/G]AAAAGAAAAACCACC	15239
rs584691796	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120477737	CCCTGCCAGGGAGAA[A/G]AATCTCTTCCATACT	15239
rs584839215	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473266	TTTTTTTGGAAGGAA[A/G]GAAGGAAGCCAGCCA	15239
rs584897541	snp	A/C			intron-variant	Hgs	GRCm38.p3	11:120481322	CCTGGCTAACCAGAA[A/C]CTCATAGAGATCCAC	15239
rs584950111	snp	G/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120467977	TGGGGGTCCGTGACG[G/T]ACCTCTCTTCCTCCG	15239
rs585094752	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120468580	GAGAAATCATCCCTC[A/G]TCTTCTAGAGCTTGC	15239
rs585203815	snp	G/T			intron-variant	Hgs	GRCm38.p3	11:120481956	TGTGTGTGTGTGTGA[G/T]AAGCAAACTAGGTTC	15239
rs585379863	snp	A/T			downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	GRCm38.p3	11:120484347	GGCGGTTCCGCCTAG[A/T]GAGCTCTTGGGAGGA	15239
rs585399827	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120467775	CTAGGTAACGCGTCC[A/G]CCCGTCAGCTCCAAG	15239
rs585556313	snp	A/C/G/T			intron-variant	Hgs	GRCm38.p3	11:120480335	CCCTCCCTCCCCCCC[A/C/G/T]CCCCCCCCCCTCTCT	15239
rs585569992	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120473543	GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT	15239
rs585608406	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120473894	ACTAGGCTAGTTGCA[A/G]TGGTGTACACTTTTA	15239
rs585633484	snp	A/C			intron-variant	Hgs	GRCm38.p3	11:120473611	ACAAACAAACAAAAA[A/C]ACTGAAAAGAAAAAC	15239
rs585744593	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120481497	TATAGGAGCCTGAGC[C/T]ACCTGACATGGGAAC	15239
rs585757775	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120479062	TCACCCTGCTGTGGC[A/G]CTCAGCTACCCACTG	15239
rs586351981	snp	A/G			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	GRCm38.p3	11:120482872	TATGCAGGTAAAGAG[A/G]CCTAGTCTTTGCTAG	15239
rs586420802	snp	G/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	GRCm38.p3	11:120467335	CTGCCTGGGACTCCC[G/T]GCCTGCCCACTCGGC	15239
rs586448351	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120478841	GGACCCAGTATTCTG[C/T]AGCCTCAGAGGCGGC	15239
rs586613052	snp	C/G			intron-variant	Hgs	GRCm38.p3	11:120481063	ATGTGTATCTGTGCA[C/G]CACAGGTGAGCTGGG	15239
rs586767839	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120471873	AAACACTAAAGTCTA[A/G]AGCTAATCAGGTTTC	15239
rs586791047	snp	A/G			missense, upstream-variant-2KB	Hgs, Mrpl12	GRCm38.p3	11:120482809	ACAGACCAGCAACAT[A/G]GGCTACATGGGGAGC	15239
rs586805014	snp	G/T			intron-variant	Hgs	GRCm38.p3	11:120476055	GCCCAAGAGGCATGT[G/T]TAATTGTGTACATGA	15239
rs587211669	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120482303	AACAAAAAGAACTTG[A/G]TTCTTTTTTTTTTTT	15239
rs587213680	snp	A/G			upstream-variant-2KB, synonymous-codon	Hgs, Arl16	GRCm38.p3	11:120465806	TTCCTCCATGGTCAT[A/G]TAACAGGGTAGGTCA	15239
rs587280122	snp	C/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	GRCm38.p3	11:120469573	TAATTCCTACCCCCC[C/T]GCCCCTTTTTTTCCC	15239
rs587297469	snp	A/G			intron-variant	Hgs	GRCm38.p3	11:120480628	TGGTTCTACTTCCGT[A/G]TGCCACAGGCTACAT	15239
rs587450125	snp	C/T			intron-variant	Hgs	GRCm38.p3	11:120473049	TCTGGCATTTACACG[C/T]GCTCTGGTACTGGCT	15239
rs864279175	snp	A/C/T			intron-variant	Hgs	GRCm38.p3	11:120480344	CCCCCCACCCCCCCC[A/C/T]CTCTCTCTCTCTCCC	15239
rs864302251	in-del	-/CT			upstream-variant-2KB, frameshift-variant	Hgs, Arl16	GRCm38.p3	11:120467239	ATCTCCGGAGCTCAG[-/CT]GTCCCGGCGGTCAAG	15239