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

Nosip

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs31097134	snp	C/T	0.444444	0.157135	utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078345	ATTAAAGGCGTGCGC[C/T]ACCACGCCCGGCTGT	66394
rs31153364	snp	C/G	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45071539	TTGGAGCTTTGCTTT[C/G]TTTGAAGAACACAGA	66394
rs31158750	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064318	CACCCCCAGTTCTTG[A/G]CAGTCTCTAAACTCG	66394
rs31179735	snp	C/T	0.444444	0.157135	intron-variant	Nosip	Mm_Celera	7:45069516	TTGTGAGCCACCATG[C/T]CAGTGCTGGAAGTTG	66394
rs31207243	snp	G/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45064811	TTGTTTTTGAGCAGG[G/T]TTTCTCTGTGCAGAC	66394
rs31237463	snp	A/C	0.277778	0.248452	intron-variant	Nosip	Mm_Celera	7:45066730	GCTTAGACTTACAGT[A/C]CCTCTGAGAAAATGA	66394
rs31336198	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070563	TCTGAGACAGGGTCT[C/T]TCTCAGTTCTTACTG	66394
rs31345396	snp	A/T	0.265928	0.249492	intron-variant	Nosip	Mm_Celera	7:45070778	AGAGGATTCCACCCC[A/T]TTGGGCCCTGCCTAC	66394
rs31377748	snp	C/G	0.5	0	intron-variant	Nosip	Mm_Celera	7:45067124	AGAGTCTTGGGGAAA[C/G]GGTGGTAAGGTGCTA	66394
rs31383397	snp	A/G	0.401235	0.199068	intron-variant	Nosip	Mm_Celera	7:45066880	CTCAAATAGGAAACA[A/G]ACTTTTTTTTTATAA	66394
rs31388296	snp	A/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070120	GGGCATCAGATCCCA[A/T]TGCAGATGGTTATGA	66394
rs31432176	snp	A/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45066891	AACAAACTTTTTTTT[A/T]ATAATTTAAGTGACT	66394
rs31441324	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061077	CTCTGCCTCCCAAGC[A/G]CTGGGATTAAAGGTG	66394
rs31486074	snp	A/G	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070763	GATAGAGGGAGGGAG[A/G]GAGGATTCCACCCCT	66394
rs31525488	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062954	TCTAGAACTCGCTAT[A/G]TAGTTAGCCTCAAAC	66394
rs31591839	snp	A/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070043	TAAATCTTTTTTTTT[A/T]AAGATTTATTTATTT	66394
rs31598675	snp	C/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063660	GCACTGTCTACAGAG[C/G]CCAGAAGGCCATTAG	66394
rs31653574	snp	A/G	0.375	0.216506	intron-variant, missense	Nosip	Mm_Celera	7:45076237	AACACAGGTGACAAG[A/G]AATACCTGCCCTTGG	66394
rs31689137	snp	A/C	0.375	0.216506	synonymous-codon	Nosip	Mm_Celera	7:45077320	TCTCTAGGGCGGCAC[A/C]GGCTTTGCGGGCTCC	66394
rs31701846	snp	A/C	0.444444	0.157135	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062971	AGTTAGCCTCAAACT[A/C]ACAAAGATCCGCCAA	66394
rs31706287	snp	G/T	0.375	0.216506	utr-variant-3-prime	Nosip	Mm_Celera	7:45077838	ACCCTCATCCCTGCC[G/T]CCAAGTAAAAATAGC	66394
rs31711374	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063085	GTTTTTGTTTTTTGG[C/T]TTTTCGAGACAGGGT	66394
rs31730498	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45075886	GGAGGAGGACTGGGT[C/T]CCATATTGAGTAGGA	66394
rs31760746	snp	A/G	0.265928	0.249492	intron-variant	Nosip	Mm_Celera	7:45070444	ATACATGTAGAGAGC[A/G]GACAATTCTTCCATG	66394
rs31762319	snp	A/G	0.265928	0.249492	utr-variant-3-prime	Nosip	Mm_Celera	7:45077524	CCAGGCAGAAACCCC[A/G]GCGTGAACCTGTGGG	66394
rs31769138	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45064923	GGTGAAAGCTATGTA[C/T]CATGCCTGGCTGTAC	66394
rs31769310	snp	A/G	0.265928	0.249492	intron-variant	Nosip	Mm_Celera	7:45071413	AAATCAGGTTAAAAT[A/G]GGAACCAATGAAAAT	66394
rs31776630	snp	A/G	0.277778	0.248452	intron-variant	Nosip	Mm_Celera	7:45065912	AGTCACGTGTGGGGA[A/G]CAGGTTCCCTACCGT	66394
rs31783193	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064425	TTATGGCCTGTTTGC[A/G]GATGAACAGTCTGTT	66394
rs31815415	snp	A/T	0.255	0.24995	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063855	TTTCTTGAGATGCAC[A/T]ACCTGGTACTGAAAT	66394
rs31840602	snp	C/T	0.265928	0.249492	intron-variant	Nosip	Mm_Celera	7:45071505	TGTATGTATGTGTTT[C/T]ACATGGGTAGTGACA	66394
rs31894656	snp	G/T	0.265928	0.249492	intron-variant	Nosip	Mm_Celera	7:45064979	CACCTTCCTAACTGA[G/T]CTGGGCCGCAGGCTT	66394
rs31901058	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45069712	TTGGCACCAGGCACA[C/T]ATGTTGTGTATAGAC	66394
rs31935039	snp	A/G	0.255	0.24995	intron-variant	Nosip	Mm_Celera	7:45076435	GAAAAGCCGGTGAGG[A/G]CCCAATGTCCAGGAT	66394
rs32029051	snp	A/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070234	TGGCTCCAAAGTTAA[A/T]TACACCGGGCTTGGT	66394
rs32058838	snp	A/G	0.32	0.24	intron-variant	Nosip	Mm_Celera	7:45076477	CAGTCCGTTCTCCCC[A/G]CCCCTCATGCCCCTT	66394
rs32076582	snp	A/G	0.387812	0.208586	intron-variant	Nosip	Mm_Celera	7:45066943	CTGTGAGTTGTGGCT[A/G]AAGCCCCTGCAGCTC	66394
rs32092666	snp	A/G	0.444444	0.157135	intron-variant	Nosip	Mm_Celera	7:45066784	AGTCCTGTCTTCGCA[A/G]CCCTTAGAAGGCTGA	66394
rs32101165	snp	A/G	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45067326	TGTGGCTCAGAGGCA[A/G]AGCCCCTAGAATCCT	66394
rs32156322	snp	G/T	0.387812	0.208586	intron-variant	Nosip	Mm_Celera	7:45066201	TTCTTCTCTCCTGTG[G/T]TGGTCTCCTCTGACT	66394
rs32176447	snp	A/G	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070469	TCCATGGCACAGGAG[A/G]TTGAACTCAGGTTAT	66394
rs32203984	snp	G/T	0.32	0.24	utr-variant-3-prime	Nosip	Mm_Celera	7:45077387	ATGCAGGCCTGAGCC[G/T]TGGCCTAATAAACGT	66394
rs32233831	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070353	GAGGCCAGCCTAGCC[C/T]TTTTGAGACCTGTTG	66394
rs32279047	snp	A/G	0.255	0.24995	intron-variant	Nosip	Mm_Celera	7:45065859	GCTGGTTAGCTTTTG[A/G]TGGTAGACTGACAAT	66394
rs32295611	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45069723	CACACATGTTGTGTA[C/T]AGACATCCATGCAGG	66394
rs32321721	snp	A/G	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45075935	CAGGGCCACCTTAGC[A/G]AAAGAACACGAAAGT	66394
rs32369475	snp	A/G	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime	Nosip, Prrg2	Mm_Celera	7:45062414	GCGACTAGGGGCAGA[A/G]TTATTTCCGGTCTCC	66394
rs32381615	snp	A/G	0.375	0.216506	utr-variant-3-prime	Nosip	Mm_Celera	7:45077479	TGCGGTGTGGGCCTG[A/G]GCTCCTGGGATTTAC	66394
rs32382775	snp	A/T	0.444444	0.157135	intron-variant	Nosip	Mm_Celera	7:45071232	GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGACAG	66394
rs32397927	snp	C/T	0.387812	0.208586	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062663	AGCGCTCTTGAACGC[C/T]TAGGTTGGAAGACGA	66394
rs32401407	snp	C/G	0.375	0.216506	utr-variant-3-prime	Nosip	Mm_Celera	7:45077839	CCCTCATCCCTGCCT[C/G]CAAGTAAAAATAGCT	66394
rs32440945	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070369	TTTTGAGACCTGTTG[C/T]GGAAACCATTGGGTG	66394
rs32444111	snp	C/T	0.32	0.24	intron-variant	Nosip	Mm_Celera	7:45071647	ATGATTTGCCTTGTG[C/T]CCTAGCAGAGGTGTA	66394
rs36243007	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45073632	TGGCTTTCTAATTCT[A/G]CCCTGTTGTCCTGTT	66394
rs36262509	snp	G/T	0.124444	0.216185	utr-variant-5-prime, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062494	TTCCGGTTCGGGACG[G/T]AGTTGAAGCAACGAC	66394
rs36266967	snp	A/C	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45075971	CAACTGTTGCCAGTT[A/C]TGCCAGAGCTGCCCA	66394
rs36275742	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075313	GGCACCCGGGCTTCA[C/T]AGGCCAAGCACCTGC	66394
rs36301613	snp	C/T	0.244898	0.249948	intron-variant	Nosip	Mm_Celera	7:45074184	CAGGCAGCTCACCTC[C/T]ACCACAGGTGCAGTT	66394
rs36331368	snp	C/T	0.231111	0.249285	synonymous-codon	Nosip	Mm_Celera	7:45076173	GAAGGAGGCGGCCAT[C/T]GTGAGCCGGCCCCTC	66394
rs36351829	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064291	CCACATTCTTTGCCA[C/T]TTAGTCTTTCTCACC	66394
rs36395487	snp	A/C	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075146	CCTGTGCTTGGTCTT[A/C]CGCTGTACAATGGCC	66394
rs36428750	snp	A/G	0.124444	0.216185	intron-variant	Nosip	Mm_Celera	7:45068925	CCATGCCCGTGAAAC[A/G]GGAACTTCATCTTGA	66394
rs36429432	snp	A/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45067790	GAGGAGACATATAGG[A/T]GAGTGTGACTGTGGC	66394
rs36431943	snp	C/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063315	TTAAGATTTATTAGC[C/T]GGGCAGTGGCAAAAA	66394
rs36480189	snp	A/G	0.124444	0.216185	intron-variant	Nosip	Mm_Celera	7:45066704	GTCATCACCACCACT[A/G]TGTTACCCAAGCTTA	66394
rs36508521	snp	C/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45068515	GTGGACATAAATTGA[C/G]TACACTCCGTAGATG	66394
rs36543664	snp	C/G	0.124444	0.216185	downstream-variant-500B	Nosip	Mm_Celera	7:45078704	CAGATGTCCACCTGC[C/G]GCCACTAGAGGGCAG	66394
rs36566831	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45068846	TTTTATTTCTTGTTG[C/T]GCTCTGCTAGAATTC	66394
rs36624351	snp	A/C	0.244898	0.249948	downstream-variant-500B	Nosip	Mm_Celera	7:45078960	CACACAGGGACACAC[A/C]AAATACAGATGTTAC	66394
rs36643967	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45067011	CCAGTCTCCATAGGC[C/T]TCTCTCTCAGTGGCA	66394
rs36646969	snp	A/T	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45066515	AATTATCCAGGTGGT[A/T]ACAGCTTGTTTTTTC	66394
rs36676612	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075492	ACCTCAGCTGGGTGA[C/T]CCAGGGAGTCTCCAG	66394
rs36680693	snp	A/G	0.260355	0.249785	intron-variant	Nosip	Mm_Celera	7:45076963	ACCGCAGCCCTCACC[A/G]CAGCCCGCACCCCAT	66394
rs36726102	snp	A/G	0.336735	0.234472	intron-variant	Nosip	Mm_Celera	7:45074443	AAAGAGAGGACTGAA[A/G]GGAGTGCTGTGAAGA	66394
rs36774951	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075185	GAAGCTAGAGGGTGC[A/G]CAGAGCAAGTGCAAG	66394
rs36778793	snp	C/T	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45070969	TCTCACTAAGTTACT[C/T]AGGCCAGGACACTAA	66394
rs36786690	snp	A/G	0.231111	0.249285	utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078406	CACTGGCCATGCAGT[A/G]ATGAGAAGATGTGTT	66394
rs36801561	snp	A/G	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45067537	CACCACAAGTCAAGG[A/G]CACATCAATCAATTG	66394
rs37000550	snp	C/T	0.391111	0.206368	downstream-variant-500B	Nosip	Mm_Celera	7:45078597	TGGGTCTTTCCTGTG[C/T]GCGTAGTTTGCTGCT	66394
rs37004280	snp	A/T	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45066356	GCAACAGACCAAACC[A/T]CGGCTAGTTGGCTTC	66394
rs37082874	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45068401	CTCAGTATTGAGTCT[A/G]TGTAAATGTACTGAA	66394
rs37125465	snp	A/G	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45074854	GGCAGGGCAGTTTCT[A/G]CAATGGTGGCGTCTG	66394
rs37162593	snp	A/G	0.260355	0.249785	intron-variant	Nosip	Mm_Celera	7:45073372	GACTGCTGTGGTTTA[A/G]GGCTGTGTTTTCGGC	66394
rs37179324	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45077092	GTTGGCTCTTCTATG[A/G]CACTGTTTTCTTTCT	66394
rs37190410	snp	C/T	0.231111	0.249285	intron-variant	Nosip	GRCm38.p3	7:45071132	TGGAAGAGCAGTGAC[C/T]GCTGGAAGAGCAGTC	66394
rs37209184	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45069865	CTGGAGGTGGCTAGC[C/T]CAGCTGGTCCTTGCT	66394
rs37233658	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45076803	GGGGCTGACTTTTGG[C/T]ACTGTCTTCCACTGT	66394
rs37237238	snp	A/G	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45073070	TGCAGTTCCGCATGC[A/G]CACACTTGCCTAGCA	66394
rs37257687	snp	A/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45073404	ACCTGAACAGGCTTC[A/T]GGAGCAGGCTACTGA	66394
rs37296873	snp	A/G	0.231111	0.249285	downstream-variant-500B	Nosip	Mm_Celera	7:45078718	CGGCCACTAGAGGGC[A/G]GAACGTCACTGCCGA	66394
rs37318155	snp	C/T	0.231111	0.249285	downstream-variant-500B	Nosip	Mm_Celera	7:45078553	TTTCACTGCCCTTGT[C/T]GCACATTACCGGAGT	66394
rs37327208	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45067761	GCCTCAACGTCCTGG[A/G]CAAAGGAGACCCTGA	66394
rs37387748	snp	A/G	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45075101	CCAGGCACTTAGCAG[A/G]GGCTTGAGATGTAAA	66394
rs37403962	snp	A/G	0.391111	0.206368	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063252	TTTTGAGGCAAGGTG[A/G]CATGTAGTCCAGGCT	66394
rs37460934	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45069893	GCTTGGTGACAGTCA[C/T]AGGAAACCCTGTGGT	66394
rs37486489	snp	A/C	0.391111	0.206368	utr-variant-3-prime	Nosip	Mm_Celera	7:45077441	GCGCCTCATTGTAGG[A/C]CCGGCGACAGAAGGA	66394
rs37598419	snp	A/G	0.231111	0.249285	synonymous-codon	Nosip	Mm_Celera	7:45074034	CCGGGACGCTGTGAA[A/G]GACTTTGACTGCTGC	66394
rs37634098	snp	A/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062699	ATTTCCCAGGATGCC[A/T]TGTACTGTCTCCCTC	66394
rs37753649	snp	C/G	0.497778	0.0332592	intron-variant	Nosip	Mm_Celera	7:45074937	AGCATCCGCATAGAC[C/G]TCCTGCGGGCCAGGC	66394
rs37755133	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45069291	GCCCTGAGTCACTCC[C/T]TTCCGTTGTTTGTTT	66394
rs37785325	snp	A/G	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45068918	TTCCTTTCCATGCCC[A/G]TGAAACGGGAACTTC	66394
rs37805698	snp	A/G	0.124444	0.216185	downstream-variant-500B	Nosip	Mm_Celera	7:45078766	AAACAGGCTGGGGCT[A/G]AGAGTCCACAGACTG	66394
rs37859254	snp	A/G	0.336735	0.234472	intron-variant	Nosip	Mm_Celera	7:45073040	AGAGATGAGAAACAT[A/G]GGGAAGGCTGGGGAT	66394
rs37881924	snp	C/T	0.32	0.24	intron-variant	Nosip	Mm_Celera	7:45071479	TTTCTGGTGAAACCT[C/T]TTCTTTAGTTTGTAT	66394
rs37898081	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45076995	CTAGCCTGCACTGCA[A/G]ACTGTCCCCTGGTGT	66394
rs37932243	snp	A/C	0.231111	0.249285	downstream-variant-500B	Nosip	Mm_Celera	7:45078648	ATACTGTCAAGGACA[A/C]AACCTTTCAAAGATT	66394
rs37969885	snp	A/G	0.231111	0.249285	downstream-variant-500B	Nosip	Mm_Celera	7:45078723	ACTAGAGGGCAGAAC[A/G]TCACTGCCGATGAGA	66394
rs38048805	snp	C/T	0.231111	0.249285	downstream-variant-500B	Nosip	Mm_Celera	7:45078515	AGGCATAGTGGTGTG[C/T]GCCTGTAACACTGAC	66394
rs38144386	snp	C/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075708	GCACTTTAGAAACTT[C/G]GCCTTGTGGCTGGGG	66394
rs38149293	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075215	GACACAAATAGATAA[C/T]CTAAGTGCCCAGCAG	66394
rs38365198	snp	A/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075423	GCTAGACTCTCCCTG[A/T]CCTTGGTTCCCTCAT	66394
rs38374104	snp	A/T	0.231111	0.249285	utr-variant-5-prime, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062471	AGAGTTTAAAAACAG[A/T]ACTCTTTTTCCGGTT	66394
rs38422029	snp	C/G	0.231111	0.249285	downstream-variant-500B	Nosip	Mm_Celera	7:45078777	GGCTGAGAGTCCACA[C/G]ACTGGAAGGTGTGAG	66394
rs38423642	snp	A/G	0.231111	0.249285	downstream-variant-500B	Nosip	Mm_Celera	7:45078984	ATGTTACCCAAGTAC[A/G]TAAAGTAACCAGAAA	66394
rs38445674	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45074168	GAGCCCTCACCAGAG[A/G]CAGGCAGCTCACCTC	66394
rs38472869	snp	G/T	0.132653	0.220748	utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078436	TCAATGTGTGGCAAC[G/T]TGTGTATTTATAATT	66394
rs38591119	snp	C/T	0.260355	0.249785	utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078490	AATATTTAAACAAAA[C/T]GTATATTCCAGGCAT	66394
rs38746536	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45073920	CTACACACTTCTCTG[C/T]GACATTTGGTGGAGG	66394
rs38917422	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063275	TCCAGGCTGCATCGA[A/G]TTTCACTAAATATCT	66394
rs39041630	snp	G/T	0.32	0.24	intron-variant	Nosip	Mm_Celera	7:45073881	TGACCTAGCCATTGT[G/T]GACTCTCTCAGACTC	66394
rs39113931	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45073847	TGAGCCTCTTCACCC[C/T]GCTTCTGGGGAAAAA	66394
rs39237361	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45074884	GCCTGGAATGCCATC[C/T]ACCTCCCGCTTCTCT	66394
rs39431109	snp	A/C	0.408163	0.193609	utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078385	TCTTGATGGAAAAAA[A/C]CAAAACACTGGCCAT	66394
rs39568677	snp	A/C	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075419	GCTAGCTAGACTCTC[A/C]CTGACCTTGGTTCCC	66394
rs39604997	snp	A/G	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45073597	TCACTGTCACCTTCA[A/G]TTTCACCCTTTGTGA	66394
rs45870789	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45072397	CTCACAGCCACCTGT[A/T]ACTCTGGCTTCAGAG	66394
rs46002966	snp	A/C			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062940	GTAGCCCTTGCTGTT[A/C]TAGAACTCGCTATGT	66394
rs46208191	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45074376	CCTTCAAGGCAAGCC[C/T]CAGCTACATAGTAGT	66394
rs46791439	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45071884	GGGAGCTTGATGCCC[A/G]TAATGAGCAGGAGGT	66394
rs46895224	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45068098	GTGGCCCACAACCAC[A/G]TGGTGGCTCACAACC	66394
rs47027117	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45071731	GTTTTCAGAGGGTCT[A/C]TAAATGCTAGGGCCC	66394
rs47570536	snp	C/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061259	ATAAGCACACAGTTG[C/G]TGAGGCTTGCTTTCT	66394
rs47582994	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45077295	ACCTCCAGCTTGTTC[C/T]TTTCTCTCCTCTCTA	66394
rs47910596	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45074279	ATGCAGGAACCTCTG[G/T]TCCATCCCAGCACCA	66394
rs48036773	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074413	CTAGCCTGAGCTCCA[A/G]TACATTGTCTCTCTA	66394
rs48102731	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45074255	CTCGGGGTACAGTGC[G/T]TGCCTCGCATGCAGG	66394
rs48238965	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45068632	TTTTTTTAAAGATTT[A/G]TTTTTTATGTGCATT	66394
rs48344835	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45073198	GAGTTTTTTTTTTTT[G/T]TTTTTGTTTTTAAAG	66394
rs48746788	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45073169	AAGATCAGCCTGGGC[A/C]ATAGAGGAAGACAGA	66394
rs48905901	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45077259	AACCCCCACTGCTGC[C/T]GGGAGCCCAGCCTGT	66394
rs49028662	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45067143	GGTAAGGTGCTAAAC[C/T]GGTACCCTACCATTA	66394
rs49202095	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45072438	CCTCTTCTGGTCTTG[G/T]CAGGCATTGCTGCAC	66394
rs49204564	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074188	CAGCTCACCTCCACC[A/G]CAGGTGCAGTTGGGC	66394
rs49277713	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45071929	TCCGCCCCCTTCCCA[A/G]CCCTTTTCTTCCCAT	66394
rs49888303	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45073220	TTTTTAAAGTGGTTC[A/C]GGCCTTTAAACCAGC	66394
rs49941284	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45073343	GTGTTCTGTCCTCCC[C/T]GCTGAGACCCACGGA	66394
rs49953750	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45071957	CATCCTTTTTCCTCT[C/T]TCTAGTGTTGGGGGT	66394
rs50472194	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45073099	CACAGACGTGGTGGC[A/T]CAGCCTGTCTTCCCA	66394
rs50558990	snp	A/C			downstream-variant-500B	Nosip	Mm_Celera	7:45078958	CACACACAGGGACAC[A/C]CCAAATACAGATGTT	66394
rs50786945	snp	C/G/T			intron-variant	Nosip	GRCm38.p3	7:45071883	AGGGAGCTTGATGCC[C/G/T]ATAATGAGCAGGAGG	66394
rs50990496	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074117	GGCAAAGGGGCAGCT[A/G]GTGTGTGTGGGTTTA	66394
rs51085300	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45072199	ACAAACACAAAAAAC[A/G]AAACAACCCAAGTGA	66394
rs51142095	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45067144	GTAAGGTGCTAAACT[G/T]GTACCCTACCATTAA	66394
rs51577025	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45073239	CTTTAAACCAGCTCT[C/T]AGGGGGCAGAGGTAG	66394
rs52192869	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45071133	GGAAGAGCAGTGACT[A/G]CTGGAAGAGCAGTCA	66394
rs52210972	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45072955	CTTAACCCCTGAGTC[A/G]TCTCCCTACCCCCTC	66394
rs52332233	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45072133	CAAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC	66394
rs52371720	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45071062	AAGAACATGATACTA[A/G]GTTTTATTTATTTAT	66394
rs52562057	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45072154	GTTCCAGGACAGCCA[A/G]GGCTGTCTCAAAAAC	66394
rs108508704	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45067436	GAGGTAGAGCCTCTA[C/T]CTTGCAACCTTGCAG	66394
rs211756474	in-del	-/G			intron-variant	Nosip	Mm_Celera	7:45074243	GGCTGAGGCTGACTC[-/G]GGGTACAGTGCGTGC	66394
rs211973637	snp	C/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061668	TGTGCAAAGGGGTAG[C/G]CAAGAGGGGAGGGGA	66394
rs212065661	snp	C/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45060655	GAATCTAGGAAGTCT[C/T]CTGGCTAGGGAGAGG	66394
rs212145171	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45069584	GAAGAGGACTCCTCC[A/G]GTTCTCTTTCAGAGG	66394
rs212159087	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45072327	TGGAGAGATGGCTCA[A/T]CCATTAGTAATGATG	66394
rs212175912	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45066483	TGTGGCTCAGTGGGT[-/A]GAATGGACCAGGATC	66394
rs212213919	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063291	TTTCACTAAATATCT[C/T]TAAGGAGATTAAGAT	66394
rs212348253	snp	C/T			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078474	CTGTAAGTCTGTTGC[C/T]AATATTTAAACAAAA	66394
rs212364702	snp	A/C			utr-variant-3-prime	Nosip	Mm_Celera	7:45078025	AGCCTAGTCTAGATG[A/C]TGGGGGCCAGGCTTG	66394
rs212412349	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062711	GCCTTGTACTGTCTC[C/T]CTCATCCTGGCTGGT	66394
rs212605260	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45066846	CCTGAGCTATATGCA[G/T]TATGAGACACAGACA	66394
rs212644767	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45071290	GATCCATCCCCTGGG[A/G]CTGTGTCTATAGGAG	66394
rs212662945	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45067350	GAATCCTCCAATGAG[A/G]GGTAGGGAATGTGGC	66394
rs212731906	in-del	-/GGG			downstream-variant-500B	Nosip	Mm_Celera	7:45078570	ACATTACCGGAGTGT[-/GGG]GTGGGGGCACCTGGG	66394
rs212751733	in-del	-/GAGTT			intron-variant	Nosip	Mm_Celera	7:45073184	ATAGAGGAAGACAGA[-/GAGTT]GTTTTTTTTTTTTGT	66394
rs212891596	snp	G/T			synonymous-codon	Nosip	Mm_Celera	7:45076092	GAAGCAGCGAGGAGC[G/T]AGGAGAGAAGAGCAG	66394
rs213151477	in-del	-/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062783	AGTGAGGGGGAACTT[-/G]GGGGTTCCCTGTGTT	66394
rs213194946	in-del	-/AAAAA			intron-variant	Nosip	GRCm38.p3	7:45071822	ACAAAGAAGGAAAGG[-/AAAAA]AAAAAAATGAGATAT	66394
rs213588532	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45074561	GGGGACCCGACCCTG[C/T]GGCTGAGCCCACGCC	66394
rs213708177	snp	G/T			utr-variant-3-prime	Nosip	Mm_Celera	7:45077573	AGGACTTGGAAGAGG[G/T]TGCCCTGAACAAGAA	66394
rs213771467	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45070282	TCTAGGACTCCAGAG[A/G]TGGATGCAGGAGGAT	66394
rs213776599	snp	A/C/T			intron-variant	Nosip	Mm_Celera	7:45077032	CACCTGTCTTCCACC[A/C/T]GGCCCCCTTTTGCCC	66394
rs213881259	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45068278	GTTCGAGCCCAGCCT[C/T]GTCTATAGAACTACT	66394
rs213916864	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	Nosip, Prrg2	Mm_Celera	7:45060854	CCAGATGACAAATGC[C/T]GCAGCGGAGTTAGGA	66394
rs214045359	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45069668	GATTCCAGGGGATCC[A/G]ATACCCTCACCCCCA	66394
rs214437837	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45073800	CCGAGAGCCACAGTG[A/G]TGGTCCCCACCCCGG	66394
rs214736656	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45073117	GCCTGTCTTCCCAGC[A/G]TTGAAGAGGCTGAGG	66394
rs214815348	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45064625	AAACAAACAAACAAA[A/C]TATATATATATATTT	66394
rs214886545	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45066792	CTTCGCAGCCCTTAG[A/G]AGGCTGACGTAGGGA	66394
rs214917872	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45073878	AGCTGACCTAGCCAT[G/T]GTGGACTCTCTCAGA	66394
rs215146826	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45065670	GCTGGCCAGACTGTC[A/T]TTGGCTTTTTTTGTT	66394
rs215917375	in-del	-/TT			intron-variant	Nosip	Mm_Celera	7:45064637	AACTATATATATATA[-/TT]TTTTTATGTATGAGT	66394
rs216211463	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45073037	AGGAGAGATGAGAAA[C/T]ATAGGGAAGGCTGGG	66394
rs216236890	snp	A/G			downstream-variant-500B	Nosip	Mm_Celera	7:45078896	ACCTCCTCTCCCTAC[A/G]TAATGTAAGCAGTGG	66394
rs216287788	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45072511	ATGGTTTTGAAAAAG[G/T]CAAGGTTTTAGTTGT	66394
rs216401989	in-del	-/AA			intron-variant	Nosip	GRCm38.p3	7:45067276	CCCTATCTTAATATT[-/AA]AAAAAAAAAAAAAAT	66394
rs216674049	snp	A/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062602	TTTGCAGTTCTGAGG[A/G]AGGTAGGATAAGGTT	66394
rs216808488	in-del	-/TT			intron-variant	Nosip	Mm_Celera	7:45064635	CAAACTATATATATA[-/TT]TATTTTTATGTATGA	66394
rs216945747	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45065402	AGATTAGATTATATT[A/G]AAGGCAGGGTTCATT	66394
rs217021881	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45064578	AGCCAGGGCTATACA[C/G]AGAAACCCTGTCTCG	66394
rs217088301	snp	G/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061764	ACTGATTACCTTCTT[G/T]GGGAGGGACTCAGGT	66394
rs217104822	in-del	-/C			intron-variant	Nosip	Mm_Celera	7:45065234	TTCTCTCCCCCCCCA[-/C]ACCCCCCCCACCCCG	66394
rs217157974	snp	C/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45060568	TTCTGAAGCAGGGGG[C/T]GACCATGTGGATCTG	66394
rs217252797	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45069184	TCCAATTCCAGTAGA[A/G]GTCAGCTTTCAAGAA	66394
rs217269640	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45076000	CAGGGCTCTGTCCCC[A/C]CACTGGTGGGGTGGG	66394
rs217309262	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45068471	CGCTCACTCCTCTAT[G/T]TGAGGCAAGGCTTTC	66394
rs217517017	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063353	ATTTATTTAAAGTAA[C/T]GAGGGGGGGGATGGG	66394
rs217615467	snp	C/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061830	GGTCTTCAGTGCCAC[C/G]GCCCCACACAGAAGA	66394
rs217674012	snp	C/T			downstream-variant-500B	Nosip	Mm_Celera	7:45078943	CTGGCCTGTGGGTGT[C/T]ACACACAGGGACACA	66394
rs217754137	in-del	-/TAG			intron-variant	Nosip	Mm_Celera	7:45067687	CTTCTGAAAGGAAGT[-/TAG]TAGTCTCGGCAATCA	66394
rs217762946	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45072612	TGTGCTTGCTAGGCA[A/C]GCACTCTACCACTGA	66394
rs218241318	in-del	-/TTG			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063806	TGTTTTTTGTTTTTT[-/TTG]TTTGTTTTTTGTTTT	66394
rs218386537	snp	C/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061325	TTTAAACAAGCTCAT[C/T]ATCAACCCTCTTCCC	66394
rs218410994	in-del	-/CCCCCC			intron-variant	Nosip	GRCm38.p3	7:45077225	GGACTTATTTCTCTG[-/CCCCCC]CCCCCCCCAACAGAA	66394
rs218441105	snp	C/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45062096	GATCTTTGAAAATTG[C/T]TTTTTCTATAATAGG	66394
rs218506681	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45073090	CTTGCCTAGCACAGA[C/T]GTGGTGGCACAGCCT	66394
rs218708790	in-del	-/T			intron-variant	Nosip	Mm_Celera	7:45071030	CTTTTTCTTTTTTTC[-/T]TTTTTTTTTTTTTAA	66394
rs218736856	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45064956	GGTTTAGACCTGGGG[A/G]CAGCAAGCACCTTCC	66394
rs218748915	in-del	-/CAGA			intron-variant	Nosip	Mm_Celera	7:45067531	ACACACACCACAAGT[-/CAGA]CAAGGACACATCAAT	66394
rs218797188	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45065993	CACCTCGATCTTTCC[A/G]TTCCCAGATAAAAGA	66394
rs218819016	in-del	-/GG			intron-variant	Nosip	Mm_Celera	7:45072048	GATACAAGTGAATGT[-/GG]GGGGGGGGGGGGACG	66394
rs218966582	in-del	-/AAACAAAC			intron-variant	Nosip	Mm_Celera	7:45072165	CCAAGGCTGTCTCAA[-/AAACAAAC]AAACAAACAAACAAA	66394
rs219133633	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45070041	ATAAATCTTTTTTTT[-/A]TAAAGATTTATTTAT	66394
rs219268849	in-del	-/CAA			intron-variant	Nosip	Mm_Celera	7:45065233	TGTTCTCTCCCCCCC[-/CAA]CCCCCCCCACCCCGT	66394
rs219486898	snp	A/G			utr-variant-3-prime	Nosip	Mm_Celera	7:45077814	AACTTGCTCAAAGAG[A/G]CGCAGACCACCCTCA	66394
rs219710260	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45077266	ACTGCTGCTGGGAGC[A/C]CAGCCTGTGAGGCAC	66394
rs219782905	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45075736	GGGAGAGCTTGGTTA[A/G]TAGCATGAAGCCCTA	66394
rs219858354	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45071558	GAAGAACACAGAAAT[-/A]TTATAAGAATATGAT	66394
rs219907335	snp	C/T			intron-variant, synonymous-codon	Nosip	Mm_Celera	7:45076578	GACCTGCCCGATGTC[C/T]GGGAAGCCACTGCGC	66394
rs220100799	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074106	AGCAGGGGAGGGGCA[A/G]AGGGGCAGCTGGTGT	66394
rs220161981	snp	A/G			downstream-variant-500B	Nosip	Mm_Celera	7:45078669	TTCAAAGATTTGGAA[A/G]GGCCTCTTGGCCAGT	66394
rs220518759	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45069788	GGGTGCTTTGATAAG[A/G]GGCTGTGGTCTTCTA	66394
rs220771300	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45064785	CATTGAGCCATCTCC[C/T]CAGCCAGTTGTTGTT	66394
rs220771809	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45070486	TGAACTCAGGTTATA[C/G]GGTTTGTAAGGCAAG	66394
rs220800023	snp	A/G			synonymous-codon	Nosip	Mm_Celera	7:45074636	GTATGAGAGGGAAGC[A/G]ATCCTGGAGTACATC	66394
rs220862895	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45066984	TGTTCACTTTGTATA[C/G]CACATGGCTTCCCAG	66394
rs220886764	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45072822	TTATTTTATGTGCAC[C/T]GGTGTTTTGCCTGCA	66394
rs221150763	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45069980	GGCACCAGACACACA[G/T]GAGGGGCACAAACAT	66394
rs221154353	snp	A/G			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078256	GGGTTTCTCTGTGTA[A/G]CCCTGGCTGTCCTGG	66394
rs221239165	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45077280	CCCAGCCTGTGAGGC[A/T]CCTCCAGCTTGTTCT	66394
rs221269612	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45075685	GCCATGTGGTCATCA[A/G]AGTCTAAGCACTTTA	66394
rs221647850	in-del	-/GCTGGAAGAGCAGTGACT			intron-variant	Nosip	Mm_Celera	7:45071115	CGTAAGTACACTGTA[-/GCTGGAAGAGCAGTGACT]GCTGGAAGAGCAGTC	66394
rs221780636	snp	A/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063007	GCCGCCCAAGTGTTG[A/T]GATTAAAAGTGTGCA	66394
rs221952604	snp	A/G			downstream-variant-500B	Nosip	Mm_Celera	7:45078719	GGCCACTAGAGGGCA[A/G]AACGTCACTGCCGAT	66394
rs221991497	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45074736	GAGGGCATCGGATCC[C/T]GTTACAGATGGTTGC	66394
rs222234218	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063483	GATCCCAGAACTGGG[C/T]GCAGAGGTAGATGGA	66394
rs222257934	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45068809	AGCCGAGCCATTATT[C/T]TTCCAGCCTCCAGAT	66394
rs222523309	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45066309	ACCTGGTGCCAGCCC[C/T]TCCCCATACACACTT	66394
rs222614228	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45067709	CGGCAATCAGCAATC[C/T]ACAGTCCTCTGCTCT	66394
rs223010147	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063581	AAAGAAAAGAAATGC[C/T]TTCCTTTTATTTTAT	66394
rs223098806	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45072653	CAACCCCAGTAACTT[C/G]TTTTGTTTGCTGAGC	66394
rs223566036	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061195	TAAAGTCATTTGCCT[A/G]TTGTACCAGGTTTTC	66394
rs224100863	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063769	CTTTTAGCCACTGCC[C/T]CATCTCTCCAGCTTC	66394
rs224164707	in-del	-/AAAAAAAAAA			intron-variant, upstream-variant-2KB	Nosip, Prrg2	GRCm38.p3	7:45063325	TAGCTGGGCAGTGGC[-/AAAAAAAAAA]AAAAAAAAAAAGATT	66394
rs224386615	in-del	-/ATGCTAGC			downstream-variant-500B	Nosip	Mm_Celera	7:45078807	GTTCAGATCCCTGTA[-/ATGCTAGC]ATCAGAGACGAGGGT	66394
rs224702047	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45065410	TTATATTAAAGGCAG[C/G]GTTCATTGGGAAGCT	66394
rs224928789	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064078	GCACTCCCCTCAGTC[C/T]TGAGGAATTGAATGC	66394
rs225398203	in-del	-/C			downstream-variant-500B	Nosip	Mm_Celera	7:45078530	CGCCTGTAACACTGA[-/C]CCCCTGCTTTCACTG	66394
rs225440020	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074289	CTCTGGTCCATCCCA[A/G]CACCACAGAAAGCCG	66394
rs225595412	snp	A/C			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45062269	CGCTCTGGGTAATGC[A/C]TAGAACAGGCTAGGG	66394
rs225659413	in-del	-/TG			intron-variant	Nosip	Mm_Celera	7:45073197	AGAGTTTTTTTTTTT[-/TG]TTTTTGTTTTTAAAG	66394
rs225810762	in-del	-/TTTGTTTTTTTTGTTTGTTTTTTG			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063796	CTTCTTAATTTGTTT[-/TTTGTTTTTTTTGTTTGTTTTTTG]TTTTGTTTTGTTTTG	66394
rs226056375	snp	A/T			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078304	AGGCTGGCCTCGAAC[A/T]CAGAAATCCACCTGA	66394
rs226354082	snp	C/G			downstream-variant-500B	Nosip	Mm_Celera	7:45078824	GCTAGCATCAGAGAC[C/G]AGGGTCCCTGGGGTT	66394
rs226568278	snp	A/G			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078328	CACCTGACTCTGCTG[A/G]GATTAAAGGCGTGCG	66394
rs226672616	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45072716	TCACTTTGTAGATTC[-/A]AAGTAGTTCAAATTC	66394
rs226716455	in-del	-/C			intron-variant	Nosip	Mm_Celera	7:45072447	TCTTGGCAGGCATTG[-/C]CTGCACATGACGTCA	66394
rs226958613	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45065310	TACTCTCTAGTCTAG[A/T]CTGGCCTTGAACTCC	66394
rs227010148	snp	C/T			intron-variant	Nosip	GRCm38.p3	7:45077225	GGACTTATTTCTCTG[C/T]CCCCCCCCCCCCCAA	66394
rs227331138	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45069019	CCCTCCCTGTAGGGA[A/T]CCACACTCACCCACA	66394
rs227450789	snp	C/T			synonymous-codon	Nosip	Mm_Celera	7:45076677	ACGCAGTGAGCGCTA[C/T]GTTTGCGCAGTGACC	66394
rs227527994	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45075161	ACGCTGTACAATGGC[C/T]ACCAGGGTGAAGCTA	66394
rs227730034	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45068235	GAAACTCTCTGCGCC[C/T]AGCAGGCATAGGTCA	66394
rs227965765	in-del	-/AGA			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061420	GATCAGAGACTACAC[-/AGA]GACAGATCAGGTCGT	66394
rs227991415	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45069435	TGGTCTCTAGAGCTC[-/A]ATGTACTTAATGTCT	66394
rs228071341	snp	A/T			upstream-variant-2KB, utr-variant-5-prime, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061589	ATGCACCCACTTACC[A/T]GGCCAGGGCTGGGAG	66394
rs228137726	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45071092	TTAAGATTTATTTAT[C/T]TATTATACGTAAGTA	66394
rs228210906	snp	C/T			utr-variant-3-prime	Nosip	Mm_Celera	7:45077574	GGACTTGGAAGAGGG[C/T]GCCCTGAACAAGAAG	66394
rs228212426	in-del	-/CCCC			intron-variant	Nosip	Mm_Celera	7:45065235	TCTCTCCCCCCCCAA[-/CCCC]CCCCCCCCACCCCGT	66394
rs228239155	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45069196	AGAGGTCAGCTTTCA[A/C]GAATCTCCTTCTCTT	66394
rs228564895	in-del	-/C			intron-variant	Nosip	Mm_Celera	7:45072193	AACAAACAAACACAA[-/C]AAAACAAAACAACCC	66394
rs228591516	snp	A/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063270	TGTAGTCCAGGCTGC[A/T]TCGAATTTCACTAAA	66394
rs228937177	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45075052	CAGGCGCGCAGCCCA[C/T]GGCCCACAGGAGCAG	66394
rs228947996	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45067250	AAAAGCCAAACTAAG[G/T]TATAGATGATACCCT	66394
rs229094586	in-del	-/TTCCATGT			intron-variant	Nosip	Mm_Celera	7:45070452	GAGAGCGGACAATTC[-/TTCCATGT]TTCCATGGCACAGGA	66394
rs229345697	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45073763	TCTTAACCATTCCTG[G/T]CCAGCTCTGCCGAAA	66394
rs229537024	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45067900	ATGGCCTGTAACTGT[A/G]GGGCTCTCTTCTGAG	66394
rs229570870	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074239	TAGTGGCTGAGGCTG[A/G]CTCGGGGTACAGTGC	66394
rs230423877	in-del	-/ACACACACACACACACACACACACAC			intron-variant	Nosip	GRCm38.p3	7:45067485	CCACTGCACACACAT[-/ACACACACACACACACACACACACAC]ACACACACACACACC	66394
rs230442558	snp	A/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063484	ATCCCAGAACTGGGC[A/G]CAGAGGTAGATGGAT	66394
rs230780111	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45070928	TGCAAGAGCTCTGCC[C/T]CAGCTCTCGGCTCGA	66394
rs230793090	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062522	GACAAGCCGGATAAC[C/T]GCTCTTGAGGTAAGC	66394
rs230944978	snp	A/C			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064237	TGAACTACCCTCTCA[A/C]ACTGGACATGGTTAA	66394
rs231001045	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061686	AGAGGGGAGGGGAGG[A/G]GAGGAGGGGAGCTCC	66394
rs231037418	snp	C/G/T			intron-variant	Nosip	Mm_Celera	7:45072964	TGAGTCATCTCCCTA[C/G/T]CCCCTCCCTTGAACT	66394
rs231076899	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45064622	ACAAAACAAACAAAC[A/T]AACTATATATATATA	66394
rs231100354	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45070240	CAAAGTTAAATACAC[C/T]GGGCTTGGTGCTACC	66394
rs231311819	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45065127	ACTCTGTAAAGTAGG[A/C]TGGCCTTGAACTCAG	66394
rs231497071	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45074573	CTGCGGCTGAGCCCA[C/T]GCCAGTGCGTCCCTC	66394
rs231500970	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45072338	CTCATCCATTAGTAA[A/T]GATGGCTGCTCTTCC	66394
rs231520419	snp	A/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063121	TGTGTAGCTCTGGCT[A/G]TCCTGGAACTAGCTC	66394
rs231842037	in-del	-/T			intron-variant	Nosip	GRCm38.p3	7:45073185	TAGAGGAAGACAGAG[-/T]TTTTTTTTTTTTGTT	66394
rs231862107	snp	C/T			utr-variant-3-prime	Nosip	Mm_Celera	7:45078093	GAGCCATCTTCACCC[C/T]GTGTTTCCATCCCAT	66394
rs232058604	snp	C/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062650	GTCAATCATTAACAG[C/G]GCTCTTGAACGCCTA	66394
rs232079052	snp	G/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45060713	TCCAAACACTCACCT[G/T]CAAACTTGAAGAGAC	66394
rs232120326	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061396	ACCTGTTGCCTCATC[A/G]AGCCTCAGAGATCAG	66394
rs232133879	in-del	-/AAAC			intron-variant	Nosip	Mm_Celera	7:45072166	CCAAGGCTGTCTCAA[-/AAAC]AAACAAACAAACAAA	66394
rs232263620	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45068280	TCGAGCCCAGCCTCG[G/T]CTATAGAACTACTTC	66394
rs232500008	snp	A/C			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078487	GCTAATATTTAAACA[A/C]AACGTATATTCCAGG	66394
rs232687814	snp	A/C			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45060499	CCTGAGCAAGAGGGG[A/C]CAGAGTTTTCACCAT	66394
rs232965474	in-del	-/TAA			intron-variant	Nosip	GRCm38.p3	7:45067276	ACCCTATCTTAATAT[-/TAA]AAAAAAAAAAAATGA	66394
rs233094859	snp	A/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063451	TTTATTTAAAGGGGT[A/G]TGGTAGACACATCTT	66394
rs233105670	in-del	-/TTTC			intron-variant	Nosip	Mm_Celera	7:45071008	CCTGCCTTTGTTTCT[-/TTTC]TTTTCTTTTTCTTTT	66394
rs233114845	in-del	-/GG			intron-variant	Nosip	Mm_Celera	7:45073189	GGAAGACAGAGTTTT[-/GG]TTTTTTTTGTTTTTG	66394
rs233174536	in-del	-/CTC			intron-variant	Nosip	Mm_Celera	7:45066206	CTCTCCTGTGTTGGT[-/CTC]CTCTGACTTCCAAGC	66394
rs233180122	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45072018	GATAAAGAACCTACA[A/T]AGCAGCAAAGACTGT	66394
rs233221206	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45072520	AAAAAGTCAAGGTTT[C/T]AGTTGTTTCTAGAGT	66394
rs233567231	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45075853	CACAGTGAGTTTCAG[A/G]CCGAGGAGGCCCTCC	66394
rs234090689	snp	C/T			synonymous-codon	Nosip	Mm_Celera	7:45076737	CGCAGTGCTGCGTCC[C/T]TCGTGAGTGCGGGGT	66394
rs234178371	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45072907	TGGGTGCTGGGAATT[A/G]AACCCAGGTTCTCTG	66394
rs234182256	snp	C/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45060595	TCTGAGGGGAGAAGC[C/T]GGGGCACAGACCCTA	66394
rs234194146	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45068497	TTTCTAGGCAGTCAG[-/A]AGGTGGACATAAATT	66394
rs234416209	snp	C/T			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078443	GTGGCAACTTGTGTA[C/T]TTATAATTTTACATC	66394
rs234481261	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45067360	ATGAGGGGTAGGGAA[C/T]GTGGCTCAGAGGCAG	66394
rs234679095	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45073968	TCTTCATTCCCACCT[C/T]GTTCTGTCCCCAGCG	66394
rs234717375	in-del	-/CAATAATTTTT			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063405	AAATTCACAAAGAAC[-/CAATAATTTTT]GTAGGACATTTGAAA	66394
rs234754512	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45067277	CCCTATCTTAATATT[-/A]AAAAAAAAAAAAATG	66394
rs234754858	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45069612	AGGACTGGGGTTCAA[C/T]TCCCAACACCCACAT	66394
rs234845130	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45070302	TGCAGGAGGATAAGA[C/T]GTTCAAGGCTATCCT	66394
rs234988939	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45069669	ATTCCAGGGGATCCA[A/G]TACCCTCACCCCCAT	66394
rs235023430	snp	A/G			missense	Nosip	Mm_Celera	7:45076342	CCCAGTGTGGGTCCC[A/G]TAGGCAAGGACAAGG	66394
rs235129410	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45072615	GCTTGCTAGGCACGC[A/G]CTCTACCACTGAGCT	66394
rs235269428	in-del	-/ACAAACAAAC			intron-variant	Nosip	Mm_Celera	7:45072180	AAAACAAACAAACAA[-/ACAAACAAAC]ACAAAAAACAAAACA	66394
rs235286572	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45067712	CAATCAGCAATCTAC[A/T]GTCCTCTGCTCTAGG	66394
rs235734951	snp	C/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061848	CCCACACAGAAGAAA[C/T]AAGGCTTTCCGACAC	66394
rs235873101	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45064637	AAACTATATATATAT[A/T]TTTTTATGTATGAGT	66394
rs236056684	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074530	CTGAATATGCTTGGT[A/G]GTACCCCATGTGGAG	66394
rs236060307	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45066808	AGGCTGACGTAGGGA[A/G]ATTGCTGGGAGTTCA	66394
rs236071040	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45066871	CAGACACACCTCAAA[C/T]AGGAAACAAACTTTT	66394
rs236189208	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45065910	GAAGTCACGTGTGGG[A/G]AACAGGTTCCCTACC	66394
rs236246371	in-del	-/GCGC			intron-variant	Nosip	Mm_Celera	7:45075040	CACACTGGACCGCAG[-/GCGC]GCAGCCCACGGCCCA	66394
rs236314368	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063032	TGTGCACCACCACAC[C/T]TAGCACTTATTACCC	66394
rs236332831	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45068680	TATCTGTATGAGGGT[A/G]CCAGATCCCCTGAAA	66394
rs236412335	in-del	-/CCTGGACCCCCGGACCCCCTGGTGCC			intron-variant	Nosip	Mm_Celera	7:45074979	CACCTGCTAACCCCA[-/CCTGGACCCCCGGACCCCCTGGTGCC]CTCGTACTCACTGCT	66394
rs236487973	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062456	GGAAGTAGGAGGAGT[A/G]GAGTTTAAAAACAGT	66394
rs236510138	snp	A/C			synonymous-codon	Nosip	Mm_Celera	7:45076093	AAGCAGCGAGGAGCG[A/C]GGAGAGAAGAGCAGA	66394
rs236869191	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45073091	TTGCCTAGCACAGAC[A/G]TGGTGGCACAGCCTG	66394
rs237266162	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45071363	TGCTGAGATATATGA[A/G]TGATTACCTAAATAG	66394
rs237277071	snp	A/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062759	CGCAGTAGAGGAGTG[A/T]TGCGGACCAAGTGAG	66394
rs237497427	snp	A/T			downstream-variant-500B	Nosip	Mm_Celera	7:45078523	TGGTGTGCGCCTGTA[A/T]CACTGACCCCCTGCT	66394
rs237650987	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45065780	ACTTCAGGCTCTCTG[C/T]TTTCCAGGACTTGCA	66394
rs237805317	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45073421	GAGCAGGCTACTGAC[C/T]ACAAGCCCAGGAGGC	66394
rs238010407	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45077267	CTGCTGCTGGGAGCC[C/T]AGCCTGTGAGGCACC	66394
rs238199691	snp	A/G			missense	Nosip	Mm_Celera	7:45076633	TTCACGCAGCTGGAC[A/G]ACTCTGTGGACCGCG	66394
rs238518655	in-del	-/CCTC/CCTCC/GC			intron-variant	Nosip	Mm_Celera	7:45072783	CCCTCCCTCCCTCTG[-/CCTC/CCTCC/GC]CCCCCCCCCAAGTAA	66394
rs238673433	in-del	-/C			intron-variant, upstream-variant-2KB	Nosip, Prrg2	GRCm38.p3	7:45063045	ACCTAGCACTTATTA[-/C]CCCCCCCCCCCCGCC	66394
rs238753133	snp	C/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061815	GGACCATAGGATCAA[C/G]GTCTTCAGTGCCACG	66394
rs238821032	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45070612	AACCTCCTGCCTCAG[A/G]CTTCTGTGTCCTGGG	66394
rs238930313	in-del	-/A			utr-variant-3-prime	Nosip	Mm_Celera	7:45077599	AGAAGTGCAAGTCTC[-/A]GTGATAGCACTCCCA	66394
rs239045184	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45070034	ACATCAAAATAAATC[C/T]TTTTTTTTAAAGATT	66394
rs239050432	snp	C/T			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078278	CTGTCCTGGAACTCA[C/T]TTTGTAGACCAGGCT	66394
rs239473992	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45070493	AGGTTATAGGGTTTG[C/T]AAGGCAAGCAAGCAT	66394
rs239596190	snp	A/C/G			downstream-variant-500B	Nosip	GRCm38.p3	7:45078935	ACCCAGCTCTGGCCT[A/C/G]TGGGTGTCACACACA	66394
rs240416870	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45076044	TGGGCCCTGGTACTG[C/T]TAACCCAGGTCCCTC	66394
rs240438512	in-del	-/T			intron-variant	Nosip	Mm_Celera	7:45075383	TTGCTCCACAGACTC[-/T]TGTGTCTCCCACACA	66394
rs240963844	in-del	-/AGGAGGAAGACTGG			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45060524	CACCATTGGGCATGA[-/AGGAGGAAGACTGG]AGTCTGGAACTCTAC	66394
rs241003318	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45066024	ACACAACTTTTATTA[C/T]TTACAATAAACCTTT	66394
rs241455411	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45067762	CCTCAACGTCCTGGG[C/T]AAAGGAGACCCTGAG	66394
rs241467339	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45067819	GCACCACAGCCAGCC[A/G]GCACTTCTGGCTGGA	66394
rs241533350	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45068810	GCCGAGCCATTATTT[C/T]TCCAGCCTCCAGATC	66394
rs241591226	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45074944	GCATAGACCTCCTGC[C/G]GGCCAGGCCCTCTGG	66394
rs241594169	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45066987	TCACTTTGTATACCA[A/C]ATGGCTTCCCAGTCT	66394
rs241654476	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45075763	CCTAGGTCCCAACCC[C/T]AGCACGGATAACCAG	66394
rs241773358	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45066358	AACAGACCAAACCAC[A/G]GCTAGTTGGCTTCCT	66394
rs241870098	in-del	-/TTGT			intron-variant	Nosip	Mm_Celera	7:45069297	AGTCACTCCCTTCCG[-/TTGT]TTGTTTCTTTGTTGA	66394
rs241992055	snp	C/T			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078313	TCGAACTCAGAAATC[C/T]ACCTGACTCTGCTGG	66394
rs242189563	in-del	-/CTTC			intron-variant	Nosip	Mm_Celera	7:45072768	TCCCTCTCTCTCCCT[-/CTTC]CCCTCCCTCCCTCTG	66394
rs242286941	snp	G/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061268	CAGTTGCTGAGGCTT[G/T]CTTTCTCTACCTATC	66394
rs242334591	in-del	-/AT			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062641	GAATCCCTGTCAATC[-/AT]ATTAACAGCGCTCTT	66394
rs242349895	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45071163	AGTGCTCTTAATTGC[G/T]GAGCCATCTCTCCAA	66394
rs242409996	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45068883	CCACTGTGCTATAAT[A/G]CTTGTTTTGAAGATG	66394
rs242478117	in-del	-/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063800	TTAATTTGTTTTTTG[-/T]TTTTTTTGTTTGTTT	66394
rs242726167	in-del	-/GTGTGTGTGTGT			intron-variant	Nosip	Mm_Celera	7:45069387	TGTTTTGCAGAGGTG[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG	66394
rs242786039	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45072823	TATTTTATGTGCACT[A/G]GTGTTTTGCCTGCAT	66394
rs242907791	snp	C/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45060611	GGGGCACAGACCCTA[C/G]GATCTGAGGGAGAAG	66394
rs242976180	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061624	GCCTCTCTTCTTTAA[C/T]GAAGGCCCTCTGGGT	66394
rs243010640	snp	C/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063107	AGACAGGGTTTCTCT[C/G]TGTAGCTCTGGCTGT	66394
rs243091134	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45075469	CCTCAGGCATTGTTA[A/C]TGTCACCACCTCAGC	66394
rs243187090	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45065182	CTGGGATTGAGGGCT[A/G]CACCCCCACCACCAT	66394
rs243633574	in-del	-/T			intron-variant	Nosip	Mm_Celera	7:45074459	GAGTGCTGTGAAGAC[-/T]GTTGCCTAAAGGTAC	66394
rs243983502	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45072990	GAACTCTTCTCCTGC[C/T]TCCCCTGACCCCCAA	66394
rs244188053	snp	C/T			downstream-variant-500B	Nosip	Mm_Celera	7:45078849	GGGGTTTGCTGATGA[C/T]CCACACCATCCCATT	66394
rs244364558	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064217	AATCCGAGGCCTGGA[C/T]TACATGAACTACCCT	66394
rs244380776	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45067049	ACAGGCATTGCCTGA[A/G]CCAGCTCTTCCAGGA	66394
rs244483473	snp	C/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062710	TGCCTTGTACTGTCT[C/G]CCTCATCCTGGCTGG	66394
rs244666917	snp	C/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061336	TCATCATCAACCCTC[C/T]TCCCTTCCAGCCCAG	66394
rs244802814	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45062282	GCCTAGAACAGGCTA[A/G]GGTGTCTCCCAGAGT	66394
rs244816694	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45071616	GGCTGCTTCAGACCG[C/T]CCACAGCAGCTGACT	66394
rs245050283	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45069086	ACTTGTCTGTGGAGC[C/T]ATGACACACATTGTT	66394
rs245113131	in-del	-/GGGAATTGAACCCTGGTC			intron-variant	Nosip	Mm_Celera	7:45068735	TCTCACGTGGGTACT[-/GGGAATTGAACCCTGGTC]AGCAGGTCCTCTGGA	66394
rs245136370	snp	C/T			synonymous-codon	Nosip	Mm_Celera	7:45076683	TGAGCGCTACGTTTG[C/T]GCAGTGACCCGAGAC	66394
rs245155436	in-del	-/C			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062625	ATAAGGTTTCGCACT[-/C]CGAATCCCTGTCAAT	66394
rs245247581	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45075998	CCCAGGGCTCTGTCC[C/G]CACACTGGTGGGGTG	66394
rs245369387	in-del	-/T			intron-variant	Nosip	Mm_Celera	7:45071337	CTCCAGCCCTCTGTA[-/T]TTTTTTCTATTGCTG	66394
rs245436673	in-del	-/T			intron-variant	Nosip	Mm_Celera	7:45072048	TGATACAAGTGAATG[-/T]GGGGGGGGGGGGACG	66394
rs245632445	in-del	-/TA			intron-variant	Nosip	Mm_Celera	7:45066891	ACAAACTTTTTTTTT[-/TA]ATAATTTAAGTGACT	66394
rs245736769	snp	G/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063606	TTTTATGTAAACGAG[G/T]GTTTTGCCTGTTTTT	66394
rs245836253	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45072786	CTCCCTCCCTCTGCC[C/T]CCCCCCAAGTAATTA	66394
rs246025514	in-del	-/A			intron-variant	Nosip	GRCm38.p3	7:45067499	TACACACACACACAC[-/A]CACACACACACACAC	66394
rs246060992	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45066316	GCCAGCCCCTCCCCA[C/T]ACACACTTAGCATTC	66394
rs246173264	in-del	-/T			utr-variant-5-prime, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062475	TTAAAAACAGTACTC[-/T]TTTTTCCGGTTCGGG	66394
rs246683580	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45070303	GCAGGAGGATAAGAC[A/G]TTCAAGGCTATCCTC	66394
rs246786472	in-del	-/TTTTTTT			intron-variant	Nosip	Mm_Celera	7:45072554	TACATAGTAACTTGG[-/TTTTTTT]GTTTTTTGTTTTTTT	66394
rs246928338	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074343	CAGCACTCAGGCAAT[A/G]CAGACAGGAAGACGA	66394
rs247067822	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45073877	AAGCTGACCTAGCCA[C/T]TGTGGACTCTCTCAG	66394
rs247077933	in-del	-/GC			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061089	GCGCTGGGATTAAAG[-/GC]GTGTGCCACCACTGC	66394
rs247079458	in-del	-/G			intron-variant	Nosip	Mm_Celera	7:45072049	GATACAAGTGAATGT[-/G]GGGGGGGGGGGACGC	66394
rs247180142	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45062183	ATATTTGGGGAACTG[A/G]ATATCAGTCTCTTCG	66394
rs247365149	snp	C/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061435	CGACAGATCAGGTCG[C/T]ATATTTCTAGGTCTT	66394
rs247603545	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45065311	ACTCTCTAGTCTAGA[C/G]TGGCCTTGAACTCCT	66394
rs247684048	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064454	TTGTATGAGATATGC[C/T]GTGCCTTATTTCTCC	66394
rs247821853	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45066843	TAGCCTGAGCTATAT[A/G]CAGTATGAGACACAG	66394
rs247925711	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45076497	TCATGCCCCTTCCAC[C/T]GCCCACATGGCGGAC	66394
rs248267880	in-del	-/CCCAGCAC			intron-variant	Nosip	GRCm38.p3	7:45072071	GGGGACGCCTTTAAT[-/CCCAGCAC]CCCAGCACCCGGGAG	66394
rs248418605	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45067744	AGCTGCTTCCCCCGT[-/A]AGCCTCAACGTCCTG	66394
rs248574810	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074694	CAGGTGAAGGTGATG[A/G]AGGCTGAGGGGAGGA	66394
rs248768058	snp	A/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062651	TCAATCATTAACAGC[A/G]CTCTTGAACGCCTAG	66394
rs248833018	snp	A/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063222	TGCGCCACCACCCCA[A/G]CGATTATTGTATTTT	66394
rs248871179	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45068572	TGCCTCAGAACCCTC[C/T]CAGGTAGCTGGGGTG	66394
rs249153726	snp	C/T			intron-variant	Nosip	GRCm38.p3	7:45067510	acacacacacacaca[C/T]acacacacacacacc	66394
rs249323562	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45066659	CAAGACCCTGCCTCA[A/G]AGGACAGCCATCTGC	66394
rs249408655	snp	A/C			utr-variant-3-prime	Nosip	Mm_Celera	7:45078201	TACATTTGAGTCCTT[A/C]AATCTGGCCAAATTC	66394
rs249714437	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45075873	GGAGGCCCTCCCAGG[A/G]GGAGGACTGGGTTCC	66394
rs249851340	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45076751	CCTCGTGAGTGCGGG[A/G]TGTGGGGAGAAGAGG	66394
rs249870977	in-del	-/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063574	GAAAGGAAAAGAAAA[-/G]AAATGCTTTCCTTTT	66394
rs249968058	in-del	-/C			intron-variant	Nosip	Mm_Celera	7:45075145	CCTGTGCTTGGTCTT[-/C]ACGCTGTACAATGGC	66394
rs250087880	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45071402	ACAAAGACATGAAAT[C/T]AGGTTAAAATAGGAA	66394
rs250132900	snp	C/T			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078467	TTACATCCTGTAAGT[C/T]TGTTGCTAATATTTA	66394
rs250597680	snp	C/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45062079	GAACAGTTTAGTCTC[C/G]AGATCTTTGAAAATT	66394
rs250619419	in-del	-/AA			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45062153	AAGATGCAATGGGGG[-/AA]AAAAAATAAGTAATA	66394
rs250662875	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45070241	AAAGTTAAATACACC[A/G]GGCTTGGTGCTACCC	66394
rs250683044	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061319	TAGGCATTTAAACAA[A/G]CTCATCATCAACCCT	66394
rs250723552	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061725	TACTAGGCCCGAGCC[A/G]GCTACTGGCGAGGGG	66394
rs250864164	snp	A/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063326	TAGCTGGGCAGTGGC[A/T]AAAAAAAAAAGATTT	66394
rs251201743	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45066950	TTGTGGCTAAAGCCC[C/T]TGCAGCTCAGCTAGG	66394
rs251213241	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45067613	ATTAAACTGCATATG[C/T]GTAAAGGAGTAAAAA	66394
rs251334067	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45068250	CAGCAGGCATAGGTC[A/G]GTGGATCTCTGAGTT	66394
rs252040347	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074578	GCTGAGCCCACGCCA[A/G]TGCGTCCCTCATCCC	66394
rs252056671	in-del	-/ACCCCCC			intron-variant, upstream-variant-2KB	Nosip, Prrg2	GRCm38.p3	7:45063044	CACCTAGCACTTATT[-/ACCCCCC]CCCCCCCGCCCCATT	66394
rs252079628	in-del	-/C			intron-variant	Nosip	Mm_Celera	7:45071033	TTTCTTTTTTTCTTT[-/C]TTTTTTTTTTAATAA	66394
rs252095657	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45060560	AACTCTACTTCTGAA[A/G]CAGGGGGTGACCATG	66394
rs252135132	in-del	-/GT			intron-variant	Nosip	Mm_Celera	7:45072555	ACATAGTAACTTGGG[-/GT]TTTTTTGTTTTTTTC	66394
rs252350121	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45075722	TGGCCTTGTGGCTGG[A/G]GAGAGCTTGGTTAAT	66394
rs252446768	snp	C/T			utr-variant-3-prime	Nosip	Mm_Celera	7:45077652	CTAGACATGGACCTG[C/T]CCCCACCAAGTGCCC	66394
rs252657672	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45067760	AGCCTCAACGTCCTG[C/G]GCAAAGGAGACCCTG	66394
rs252669733	in-del	-/AGGCCC			intron-variant	Nosip	Mm_Celera	7:45065572	GCTGGGAGAACCTGG[-/AGGCCC]AGTCTGCTTTGATGT	66394
rs252892750	in-del	-/TTTATTTA			intron-variant	Nosip	Mm_Celera	7:45071064	AACATGATACTAGGT[-/TTTATTTA]TTTATTTATTTATTA	66394
rs253022866	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45069710	CCTTGGCACCAGGCA[C/T]ACATGTTGTGTATAG	66394
rs253161929	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45077178	CTGTCCAGACTCTTC[C/G]ATGTTCTGAATGCCC	66394
rs253163597	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45068836	AGATCTGAATTTTTA[C/T]TTCTTGTTGTGCTCT	66394
rs253334077	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45073786	TGCCGAAAGGAAGGC[C/G]GAGAGCCACAGTGGT	66394
rs253397577	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45073204	TTTTTTTTTGTTTTT[G/T]TTTTTAAAGTGGTTC	66394
rs253462701	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45065501	GCAGGAGGGGAGGGG[A/G]AGAAGAGAAAAAGTT	66394
rs253500247	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45072530	GGTTTTAGTTGTTTC[C/T]AGAGTGTCTTACATA	66394
rs253522297	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45072812	AATTATTTGTTTATT[A/T]TATGTGCACTGGTGT	66394
rs253554394	snp	A/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063468	GGTAGACACATCTTT[A/G]ATCCCAGAACTGGGC	66394
rs253706737	snp	G/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063077	CATTGTTCGTTTTTG[G/T]TTTTTGGCTTTTCGA	66394
rs253752490	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45075074	CAGGAGCAGCTTCCC[A/C]TGCTCTCAGCTCCAG	66394
rs253923747	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45070144	GTTATGAGCCACCAT[A/G]TGGTTGCTGGGGATT	66394
rs254196793	snp	C/T			downstream-variant-500B	Nosip	Mm_Celera	7:45078800	GGTGTGAGTTCAGAT[C/T]CCTGTAATGCTAGCA	66394
rs254227271	in-del	-/C			intron-variant	Nosip	Mm_Celera	7:45065226	TTGTTGTTGTTCTCT[-/C]CCCCCCCAACCCCCC	66394
rs254347402	snp	A/G			downstream-variant-500B	Nosip	Mm_Celera	7:45078941	CTCTGGCCTGTGGGT[A/G]TCACACACAGGGACA	66394
rs254578707	in-del	-/AG			intron-variant	Nosip	Mm_Celera	7:45065141	GATGGCCTTGAACTC[-/AG]AGATCTGGCTGCCTC	66394
rs255025076	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062524	CAAGCCGGATAACCG[C/T]TCTTGAGGTAAGCTG	66394
rs255076165	in-del	-/A			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063326	TAGCTGGGCAGTGGC[-/A]AAAAAAAAAAGATTT	66394
rs255112970	snp	A/G			synonymous-codon	Nosip	Mm_Celera	7:45076653	TGTGGACCGCGTGGG[A/G]CTCATCACACGCAGT	66394
rs255162355	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45077279	GCCCAGCCTGTGAGG[C/T]ACCTCCAGCTTGTTC	66394
rs255299471	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45075950	AAAAGAACACGAAAG[C/T]GTCAACAACTGTTGC	66394
rs255409343	snp	A/G			downstream-variant-500B	Nosip	Mm_Celera	7:45078667	CTTTCAAAGATTTGG[A/G]AGGGCCTCTTGGCCA	66394
rs255810076	in-del	-/A			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45062152	TAAGATGCAATGGGG[-/A]GAAAAAATAAGTAAT	66394
rs255837725	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45064624	AAAACAAACAAACAA[A/T]CTATATATATATATT	66394
rs255853124	in-del	-/GA			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064365	CGGCTGGGCTTTTGT[-/GA]CTGGCTTCTCTCCCG	66394
rs255976696	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45067373	AATGTGGCTCAGAGG[C/T]AGAGCCTTGCCTAGA	66394
rs256067266	in-del	-/TTTA			intron-variant	Nosip	Mm_Celera	7:45068621	ATCTTGATTTTTTTT[-/TTTA]AAGATTTATTTTTTA	66394
rs256389698	in-del	-/CCGA			intron-variant	Nosip	Mm_Celera	7:45076513	CCCACATGGCGGACC[-/CCGA]CTCTCCCTCTCCCCT	66394
rs256656684	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45077261	CCCCCACTGCTGCTG[A/G]GAGCCCAGCCTGTGA	66394
rs256674596	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45069750	CAGGCACAGCTGTAG[C/T]CCTAGCTGGCCTGAA	66394
rs257440349	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45070504	TTTGTAAGGCAAGCA[A/C]GCATCTTCACCCTGA	66394
rs257453486	snp	A/C			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45062238	TCAAACTTGAAGAGA[A/C]TCAAAGCAACTGCCC	66394
rs257483532	in-del	-/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	GRCm38.p3	7:45063356	TATTTAAAGTAACGA[-/G]GGGGGGGATGGGTGG	66394
rs257660375	snp	A/G			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078351	GGCGTGCGCTACCAC[A/G]CCCGGCTGTTGGGCA	66394
rs257702245	in-del	-/A			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078378	GCAAATTCTTGATGG[-/A]AAAAAACCAAAACAC	66394
rs257785957	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45069444	AGAGCTCATGTACTT[-/A]ATGTCTCTGGAGGTC	66394
rs257842309	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074538	GCTTGGTGGTACCCC[A/G]TGTGGAGGGGGACCC	66394
rs258034258	in-del	-/A			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064449	TCTGTTGTATGAGAT[-/A]ATGCTGTGCCTTATT	66394
rs258043631	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45068797	TCTTAACTGCTGAGC[C/T]GAGCCATTATTTTTC	66394
rs258220631	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45066336	ACTTAGCATTCCAAT[A/T]CATAGCAACAGACCA	66394
rs258246852	snp	A/G			synonymous-codon	Nosip	Mm_Celera	7:45073527	GAACTGCACTGCAGG[A/G]GCCGTCTACACCTAC	66394
rs258313766	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45074157	TCAGAGCCTCAGAGC[C/T]CTCACCAGAGGCAGG	66394
rs258799624	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45065238	CTCCCCCCCCAACCC[-/A]CCCCCACCCCGTGTG	66394
rs258812759	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074984	GCTAACCCCACCTGG[A/G]CCCCCGGACCCCCTG	66394
rs258823829	snp	C/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061188	CAGGTAGTAAAGTCA[C/T]TTGCCTATTGTACCA	66394
rs258932065	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45074434	TGTCTCTCTAAAGAG[A/C]GGACTGAAAGGAGTG	66394
rs259068862	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45065853	CTGCCTGCTGGTTAG[C/T]TTTTGATGGTAGACT	66394
rs259187244	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45066507	CAGGATCCAATTATC[A/C]AGGTGGTTACAGCTT	66394
rs259227694	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45076054	TACTGCTAACCCAGG[C/T]CCCTCTTCCCCCAGG	66394
rs259231244	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45066995	TATACCACATGGCTT[C/T]CCAGTCTCCATAGGC	66394
rs259482998	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45067150	TGCTAAACTGGTACC[C/T]TACCATTAAGCTAAG	66394
rs259484629	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45075769	TCCCAACCCCAGCAC[A/G]GATAACCAGGAATGG	66394
rs259492939	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45067841	CTGGCTGGAGAGATG[C/T]CTCAGCTTGTTTTTA	66394
rs259497297	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	Nosip, Prrg2	Mm_Celera	7:45062399	AGGCGAAGCGCCTCC[C/G]CGACTAGGGGCAGAA	66394
rs259626359	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45070116	AAGAGGGCATCAGAT[C/T]CCAATGCAGATGGTT	66394
rs259637095	snp	C/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061549	CAGGACACCAGATCC[C/T]CTGCCCAGGAGTTTC	66394
rs259637425	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45070740	CTTTTCATCTGTCAG[C/T]ACACTCAGATAGAGG	66394
rs259856105	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45071043	TTCTTTTTTTTTTTT[A/T]AATAAGAACATGATA	66394
rs260096233	in-del	-/C			intron-variant	Nosip	Mm_Celera	7:45076949	GTTGCCATTCGCTCA[-/C]CGCAGCCCTCACCGC	66394
rs260106399	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45073884	CCTAGCCATTGTGGA[C/G]TCTCTCAGACTCCAC	66394
rs260223856	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45070043	TAAATCTTTTTTTTT[-/A]AAGATTTATTTATTT	66394
rs260595681	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063505	GTAGATGGATTTTCC[C/T]GAGTTTGAGACCAGC	66394
rs260611089	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45072885	GAACTGGGTGTGAGC[A/C]ACCATGTGGGTGCTG	66394
rs260616002	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063916	TGTTCTTATTTTCAA[C/T]GAGGTTTATTGGGAT	66394
rs260676890	in-del	-/TG			intron-variant	Nosip	Mm_Celera	7:45071216	GCAGTTTATTACATT[-/TG]TGTGTGTGTGTGTGT	66394
rs260705539	snp	C/T			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078288	ACTCACTTTGTAGAC[C/T]AGGCTGGCCTCGAAC	66394
rs260708604	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45072635	ACCACTGAGCTAAAT[A/C]CCCAACCCCAGTAAC	66394
rs261091983	in-del	-/CCCACAACCACATGGTGG			intron-variant	Nosip	Mm_Celera	7:45068069	ACCCTGAGTTCAATT[-/CCCACAACCACATGGTGG]CCCACAACCACATGG	66394
rs261275081	in-del	-/TGA			downstream-variant-500B	Nosip	Mm_Celera	7:45078843	GTCCCTGGGGTTTGC[-/TGA]TGATCCACACCATCC	66394
rs261352073	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45072005	GTGAAAGGTGGAAGA[A/T]AAAGAACCTACAAAG	66394
rs261392118	in-del	-/A			intron-variant	Nosip	Mm_Celera	7:45067596	CTCATGTGACCTCAG[-/A]AATTAAACTGCATAT	66394
rs261452374	snp	A/C			utr-variant-3-prime	Nosip	Mm_Celera	7:45077449	TTGTAGGCCCGGCGA[A/C]AGAAGGAGTGGGCCT	66394
rs261588917	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45073374	CTGCTGTGGTTTAGG[G/T]CTGTGTTTTCGGCGA	66394
rs261662542	in-del	-/CCC			intron-variant	Nosip	Mm_Celera	7:45065236	TCTCTCCCCCCCCAA[-/CCC]CCCCCACCCCGTGTG	66394
rs261791900	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45068229	TTTCAGGAAACTCTC[G/T]GCGCCCAGCAGGCAT	66394
rs261816185	in-del	-/TTTGTTTTTTGTTTTTTTTG			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063789	TCTCCAGCTTCTTAA[-/TTTGTTTTTTGTTTTTTTTG]TTTGTTTTTTGTTTT	66394
rs261836412	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45075883	CCAGGAGGAGGACTG[A/G]GTTCCATATTGAGTA	66394
rs261992273	snp	A/G			upstream-variant-2KB, missense, utr-variant-5-prime	Nosip, Prrg2	Mm_Celera	7:45060816	AGAGCAGGGAAGGAC[A/G]GCCCCTCATACTGTG	66394
rs262139754	snp	A/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062765	AGAGGAGTGATGCGG[A/G]CCAAGTGAGGGGGAA	66394
rs262222292	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45060464	TGGGGTCCTAGGGGT[A/G]CGGACCAGGCCTGGA	66394
rs262268380	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45069001	CCTGAGATAGCCCCA[C/T]TCCCCTCCCTGTAGG	66394
rs262475269	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45069646	AGCTCTCAATGTCTG[A/T]AACTGCGATTCCAGG	66394
rs262544708	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45067775	GGCAAAGGAGACCCT[G/T]AGGAGACATATAGGA	66394
rs262648040	in-del	-/C			intron-variant	Nosip	Mm_Celera	7:45072379	CCAGTCCCCACATGG[-/C]AGCTCACAGCCACCT	66394
rs262725197	snp	C/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063058	TACCCCCCCCCCCCC[C/G]CCCCATTGTTCGTTT	66394
rs262763032	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45065092	AGACAGGGTTTCTCT[A/G]TGTAGTCCTGCTGAA	66394
rs262928205	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061822	AGGATCAAGGTCTTC[A/G]GTGCCACGGCCCCAC	66394
rs263226209	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45064770	AACAGTGTTCTTAAC[C/T]ATTGAGCCATCTCCC	66394
rs263658212	in-del	-/ACAGACAGACAGACAGACAGAC			intron-variant	Nosip	Mm_Celera	7:45071241	GTGTGTGAGAGAGAG[-/ACAGACAGACAGACAGACAGAC]AGACAGACAGACAGA	66394
rs263736784	snp	A/T			intron-variant	Nosip	Mm_Celera	7:45073247	CAGCTCTTAGGGGGC[A/T]GAGGTAGAGTTTGAG	66394
rs263777919	in-del	-/TT			intron-variant	Nosip	GRCm38.p3	7:45068612	GACACCAGATCTTGA[-/TT]TTTTTTTTTTTAAAG	66394
rs263843855	snp	A/G			intron-variant	Nosip	Mm_Celera	7:45074710	AGGCTGAGGGGAGGA[A/G]GACACCAGGAGAGGG	66394
rs264424527	snp	C/T			synonymous-codon	Nosip	Mm_Celera	7:45076722	CAATGCCACGCCGTG[C/T]GCAGTGCTGCGTCCC	66394
rs264428999	in-del	-/AGACAGACAGACAGAC			intron-variant	Nosip	Mm_Celera	7:45071242	GTGTGTGAGAGAGAG[-/AGACAGACAGACAGAC]AGACAGACAGACAGA	66394
rs264587395	in-del	-/TGTGTGTGTGTG			intron-variant	Nosip	Mm_Celera	7:45071215	GCAGTTTATTACATT[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT	66394
rs264624600	snp	G/T			intron-variant	Nosip	Mm_Celera	7:45070889	GTTGACCAGGCCTTG[G/T]GTGCTAGGCAAGTGC	66394
rs264651084	snp	C/T			utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078326	TCCACCTGACTCTGC[C/T]GGGATTAAAGGCGTG	66394
rs264680320	snp	A/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064225	GCCTGGACTACATGA[A/G]CTACCCTCTCAAACT	66394
rs264704039	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45072962	CCTGAGTCATCTCCC[C/T]ACCCCCTCCCTTGAA	66394
rs264783852	snp	C/G			intron-variant	Nosip	Mm_Celera	7:45076516	CACATGGCGGACCCT[C/G]TCCCTCTCCCCTATT	66394
rs264957029	snp	A/C			intron-variant	Nosip	Mm_Celera	7:45068906	TGAAGATGCAAGTTC[A/C]TTTCCATGCCCGTGA	66394
rs265169751	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061381	AGTCAGCCTCCCTCT[A/G]CCTGTTGCCTCATCG	66394
rs265554951	in-del	-/AAACA			intron-variant	Nosip	Mm_Celera	7:45064599	CCTGTCTCGAAAAAC[-/AAACA]AAACAAAACAAAACA	66394
rs265691260	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063114	GTTTCTCTGTGTAGC[C/T]CTGGCTGTCCTGGAA	66394
rs265765604	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45065186	GATTGAGGGCTGCAC[C/T]CCCACCACCATTAGG	66394
rs266027654	snp	C/T			intron-variant	Nosip	Mm_Celera	7:45073738	ACCATCCCACGTCTG[C/T]TCCCCTTCCTCTTAA	66394
rs266191081	snp	A/C			downstream-variant-500B	Nosip	Mm_Celera	7:45078755	GCTTAGAATTTAAAC[A/C]GGCTGGGGCTGAGAG	66394
rs266222484	in-del	-/A			upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45062154	AAGATGCAATGGGGG[-/A]AAAAATAAGTAATAT	66394
rs387095023	in-del	-/A			intron-variant	Nosip	GRCm38.p3	7:45071822	ACAAAGAAGGAAAGG[-/A]AAAAAAAAAAATGAG	66394
rs578814136	snp	A/G			intron-variant	Nosip	GRCm38.p3	7:45072063	TGGGGGGGGGGGGAC[A/G]CCTTTAATCCCAGCA	66394
rs578955018	snp	A/T			intron-variant	Nosip	GRCm38.p3	7:45068487	TGAGGCAAGGCTTTC[A/T]AGGCAGTCAGAGGTG	66394
rs579163600	snp	A/T			intron-variant	Nosip	GRCm38.p3	7:45071234	GTGTGTGTGTGTGTG[A/T]GAGAGAGAGACAGAC	66394
rs580075921	snp	C/G			intron-variant	Nosip	GRCm38.p3	7:45072113	CGGATTTCTGAGTTT[C/G]AGGCCAAGCCTGGTC	66394
rs580443730	snp	A/T			intron-variant	Nosip	GRCm38.p3	7:45072383	GTCCCCACATGGAGC[A/T]CACAGCCACCTGTAA	66394
rs580513411	snp	A/T			upstream-variant-2KB, intron-variant	Nosip, Prrg2	GRCm38.p3	7:45062166	GGGAAAAAATAAGTA[A/T]TATATTTGGGGAACT	66394
rs580842278	snp	G/T			intron-variant	Nosip	GRCm38.p3	7:45067695	AAGGAAGTTAGTCTC[G/T]GCAATCAGCAATCTA	66394
rs580854797	snp	C/T			intron-variant, upstream-variant-2KB	Nosip, Prrg2	GRCm38.p3	7:45063843	TGTTTTGTTTTGTTT[C/T]TTGAGATGCACAACC	66394
rs581091639	snp	C/G			intron-variant	Nosip	GRCm38.p3	7:45072779	TCCCTCCCTCCCTCC[C/G]TCTGCCCCCCCCCAA	66394
rs581233358	snp	C/T			utr-variant-3-prime, downstream-variant-500B	Nosip	GRCm38.p3	7:45078391	TGGAAAAAACCAAAA[C/T]ACTGGCCATGCAGTG	66394
rs581999782	snp	A/G			intron-variant	Nosip	GRCm38.p3	7:45072099	GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTTGA	66394
rs582855280	snp	G/T			intron-variant	Nosip	GRCm38.p3	7:45069538	TGGAAGTTGAGTCCA[G/T]GTCCTCTGTAGAAGC	66394
rs582898819	snp	A/C/G			intron-variant	Nosip	GRCm38.p3	7:45070443	CATACATGTAGAGAG[A/C/G]GGACAATTCTTCCAT	66394
rs583169704	snp	A/G			intron-variant	Nosip	GRCm38.p3	7:45074437	CTCTCTAAAGAGAGG[A/G]CTGAAAGGAGTGCTG	66394
rs583196925	snp	A/G			intron-variant	Nosip	GRCm38.p3	7:45072549	GTGTCTTACATAGTA[A/G]CTTGGGTTTTTTGTT	66394
rs583555774	snp	A/C			intron-variant	Nosip	GRCm38.p3	7:45072203	ACACAAAAAACAAAA[A/C]AACCCAAGTGAATGG	66394
rs583705154	snp	C/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	GRCm38.p3	7:45061016	CTGGCTGTCCTGGAA[C/G]TCACTCTGTAGAGCA	66394
rs583755901	snp	A/C			intron-variant, upstream-variant-2KB	Nosip, Prrg2	GRCm38.p3	7:45062780	ACCAAGTGAGGGGGA[A/C]CTTGGGGTTCCCTGT	66394
rs584204025	snp	A/T			intron-variant	Nosip	GRCm38.p3	7:45065225	TTTGTTGTTGTTCTC[A/T]CCCCCCCCAACCCCC	66394
rs584860869	snp	A/G			downstream-variant-500B	Nosip	GRCm38.p3	7:45078828	GCATCAGAGACGAGG[A/G]TCCCTGGGGTTTGCT	66394
rs584939568	snp	C/T			intron-variant	Nosip	GRCm38.p3	7:45067728	GTCCTCTGCTCTAGG[C/T]AAGCTGCTTCCCCCG	66394
rs585453944	snp	A/G			intron-variant	Nosip	GRCm38.p3	7:45072059	AATGTGGGGGGGGGG[A/G]GACGCCTTTAATCCC	66394
rs586182012	snp	C/T			intron-variant	Nosip	GRCm38.p3	7:45072112	GCGGATTTCTGAGTT[C/T]GAGGCCAAGCCTGGT	66394
rs586384905	snp	A/T			intron-variant	Nosip	GRCm38.p3	7:45072204	CACAAAAAACAAAAC[A/T]ACCCAAGTGAATGGT	66394
rs586602813	snp	C/T			intron-variant	Nosip	GRCm38.p3	7:45072767	TCTCCCTCTCTCTCC[C/T]TCCCTCCCTCCCTCT	66394
rs586766510	snp	A/G			intron-variant, upstream-variant-2KB	Nosip, Prrg2	GRCm38.p3	7:45063170	CCAACTCAGAAATCC[A/G]CCTGCCTCTGACTCC	66394
rs586773209	snp	A/G			upstream-variant-2KB, intron-variant	Nosip, Prrg2	GRCm38.p3	7:45061029	AACTCACTCTGTAGA[A/G]CAGGCTGGCCTCAAA	66394
rs586818122	snp	A/C			intron-variant	Nosip	GRCm38.p3	7:45076938	GCAGCGGGTGAGTTG[A/C]CATTCGCTCACCGCA	66394
rs587000315	snp	A/G			intron-variant	Nosip	GRCm38.p3	7:45066479	GGGATGTGGCTCAGT[A/G]GGTAGAATGGACCAG	66394