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

Ppara

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3679297	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770566	ACCTACCAGGCATGC[C/G]TAAGACTCCCACGAG	19013
rs3679322	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770578	TGCGTAAGACTCCCA[C/T]GAGCTACAGCTCATT	19013
rs3679344	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770588	TCCCACGAGCTACAG[C/G]TCATTGACAGAGTCT	19013
rs3679946	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770664	GTTGAAAGCAAAGTA[A/G]TGGTGCTTTTAAAGT	19013
rs3680606	snp	A/G	0.46875	0.121031	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770745	GCCTGGCTGTCCATC[A/G]TTGCTTATTTTTCCC	19013
rs3680770	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770821	ATGAGATGCCCTTTT[C/T]CCTTTTCTATTGAGT	19013
rs3681229	snp	A/G	0.489796	0.070696	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770830	CCTTTTCCCTTTTCT[A/G]TTGAGTTTCTGGTCA	19013
rs3681406	snp	A/G	0.46875	0.121031	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770922	CAACTGTTTGCTTAC[A/G]TGTACCTCTTATGGT	19013
rs6253977	snp	C/T	0.32	0.24	utr-variant-3-prime	Ppara	Mm_Celera	15:85802674	CCAAGGAGTCGAGGA[C/T]GTAGCCCAGTGGATG	19013
rs6254040	snp	C/T	0.290657	0.246672	utr-variant-3-prime	Ppara	Mm_Celera	15:85802711	CTTGGTTCCTGGTGC[C/T]GATTTATggacatgg	19013
rs6255204	snp	A/G	0.5	0	utr-variant-3-prime	Ppara	Mm_Celera	15:85802940	TTTGCACCCTTACTG[A/G]ccttccccnctccct	19013
rs6255595	snp	A/C	0.444444	0.157135	utr-variant-3-prime	Ppara	Mm_Celera	15:85802949	TTACTGACCTTCCCC[A/C]CTCCCTCCTGCTCTT	19013
rs6311008	snp	A/G	0.495	0.0497494	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85774379	CCTCATTACCCTACC[A/G]TTCTGGAATATCTAG	19013
rs6312031	snp	C/T	0.265928	0.249492	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85774569	TGTGTTGGGGTGTGC[C/T]CATGTGACCTCTGTT	19013
rs6313052	snp	A/G	0.487293	0.0786907	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85774741	GTGTTATCTCATCTC[A/G]TTTGTGCATGGCAAG	19013
rs8238200	snp	C/T	0.345679	0.230967	upstream-variant-2KB, utr-variant-5-prime, intron-variant	Ppara	Mm_Celera	15:85735014	TCTNAAGATCAGATT[C/T]CGCCTGTCCGTCCAC	19013
rs8238201	snp	C/T	0.18	0.24	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85735199	GCGCACCCTTCCCAC[C/T]GACTGTTCTCCCCCG	19013
rs8238202	snp	C/T	0.128419	0.218444	synonymous-codon	Ppara	Mm_Celera	15:85798088	CTTGATGAACAAAGA[C/T]GGGATGCTGATCGCG	19013
rs8238203	snp	A/T	0.113866	0.209684	synonymous-codon	Ppara	Mm_Celera	15:85798136	CACACGCGAGTTCCT[A/T]AAGAACCTGAGGAAG	19013
rs13466761	snp	A/C	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85806285	CCTTGGCGTGTCTTC[A/C]TAACTCCAAGATCCA	19013
rs13475195	snp	C/T	0.375	0.216506	intron-variant, utr-variant-3-prime, downstream-variant-500B	Ppara, Cdpf1	GRCm38.p3	15:85807102	CAAACAACACAATGT[C/T]ATCTGTCTAGGGAAT	19013
rs13475196	snp	C/T	0.444444	0.157135	intron-variant, utr-variant-3-prime, downstream-variant-500B	Ppara, Cdpf1	GRCm38.p3	15:85806997	TGACTCTGTATCATA[C/T]TTATCATTAAAAACC	19013
rs16783499	snp	A/G	0.0980975	0.198559	synonymous-codon	Ppara	GRCm38.p3	15:85791012	CTTTCCCGCGAGTAT[A/G]ACCCGGGCCTTGACC	19013
rs16783500	snp	C/T	0.188366	0.242283	intron-variant	Ppara	GRCm38.p3	15:85791087	CTGGCGCTGACATAT[C/T]GCCAAGGGACATTTC	19013
rs16783501	snp	A/T	0.0980975	0.198559	intron-variant	Ppara	Mm_Celera	15:85791128	TATTTCNTGCACTGG[A/T]CAGTGTTCTCAGCCA	19013
rs16783502	snp	A/C	0.090703	0.192677	intron-variant	Ppara	Mm_Celera	15:85791137	GATAAATTCTATTTC[A/C]TGCACTGGNCAGTGT	19013
rs16783503	snp	C/T	0.290657	0.246672	intron-variant	Ppara	Mm_Celera	15:85798282	AGTGGATCTGTCACT[C/T]GCAGGNNTTCACNGG	19013
rs16783504	snp	C/T	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85798288	TCTGTCACTNGCAGG[C/T]NTTCACNGGCTTCCC	19013
rs16783505	snp	A/G	0.235537	0.249581	intron-variant	Ppara	Mm_Celera	15:85798289	CTGTCACTNGCAGGN[A/G]TTCACNGGCTTCCCC	19013
rs16783506	snp	C/T	0.463593	0.129916	intron-variant	Ppara	GRCm38.p3	15:85798295	CTNGCAGGNNTTCAC[C/T]GGCTTCCCCTTCTNT	19013
rs16783507	snp	A/G	0.165289	0.235211	intron-variant	Ppara	Mm_Celera	15:85798309	CNGGCTTCCCCTTCT[A/G]TAGGAACTCAGTGGT	19013
rs16783508	snp	G/T	0.4352	0.167931	intron-variant	Ppara	GRCm38.p3	15:85798356	ATATGTATGCCGATA[G/T]NGTGANNTGAGCTCT	19013
rs16783509	snp	A/T	0.4352	0.167931	intron-variant	Ppara	GRCm38.p3	15:85798357	TATGTATGCCGATAN[A/T]GTGANNTGAGCTCTG	19013
rs16783510	snp	C/T	0.0849383	0.187762	intron-variant	Ppara	Mm_Celera	15:85798362	ATGCCGATANNGTGA[C/T]NTGAGCTCTGGCAGG	19013
rs16783511	snp	A/G	0.0849383	0.187762	intron-variant	Ppara	Mm_Celera	15:85798363	TGCCGATANNGTGAN[A/G]TGAGCTCTGGCAGGG	19013
rs16783512	snp	G/T	0.235537	0.249581	intron-variant	Ppara	Mm_Celera	15:85798380	GAGCTCTGGCAGGGT[G/T]GGGTGATGTCTTGAG	19013
rs16783513	snp	C/T	0.231111	0.249285	intron-variant	Ppara	Mm_Celera	15:85798401	ATGTCTTGAGTAACT[C/T]CAAATTTCTGTGGAG	19013
rs16783514	snp	A/G	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85798430	AGTGGAACTGAGTGA[A/G]AACAGTATAGCTATG	19013
rs16783515	snp	A/T	0.0849383	0.187762	intron-variant	Ppara	Mm_Celera	15:85798498	TGTATAGTAGCATAT[A/T]ATATGTATACATTAA	19013
rs16783516	snp	A/C	0.0849383	0.187762	intron-variant	Ppara	Mm_Celera	15:85798525	TTAAACATATACTCC[A/C]CTGGTAATATACAAT	19013
rs16820243	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733375	CTAGAACCCCTCAAC[A/C]CCTTAGGAAGCAAAG	19013
rs16820244	in-del	-/A/C/T	0.119908	0.219859	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733474	ATAGGACAAGTCCTT[-/A/C/T]NNNNNNTCCTCTCAA	19013
rs16820251	snp	A/G	0.18	0.24	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733492	CTCTCAATACAGTCT[A/G]TCAAACAAAATTCAC	19013
rs16820252	in-del	-/G	0.095	0.19615	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733543	GAGCCATTTGAGGAG[-/G]ANATGTTCAGGATCT	19013
rs16820254	snp	A/G	0.197531	0.244432	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733597	AGTCTATGTTCCAAA[A/G]NNATTCTTCTGGACA	19013
rs16820255	snp	A/T	0.30839	0.243086	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733598	GTCTATGTTCCAAAN[A/T]NATTCTTCTGGACAG	19013
rs16820257	snp	C/T	0.362812	0.2231	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733644	AAAACCAAACAAAAC[C/T]CCCATATTTTCTCAT	19013
rs16820258	snp	C/T	0.095	0.19615	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733670	CTCATCTTGAAACCT[C/T]GGGCGCTCCAANAAT	19013
rs16820259	snp	A/G	0.117188	0.211804	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733682	CCTNGGGCGCTCCAA[A/G]AATCCCAACTGTCAT	19013
rs16820260	snp	G/T	0.099723	0.199792	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733719	TTTCTGTGTTCTCTG[G/T]GCTCAGCAGTTACTC	19013
rs16820261	snp	A/G	0.18	0.24	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733754	GGCCCCTCTCATTCC[A/G]AACCATTCTTTCCAN	19013
rs16820262	snp	A/G	0.473373	0.11227	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733769	NAACCATTCTTTCCA[A/G]ATTATTCCAAATGTC	19013
rs16820263	snp	A/G	0.152778	0.230321	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733790	TCCAAATGTCTGGTA[A/G]AACTGGGTTAACAGC	19013
rs16820264	snp	C/G	0.095	0.19615	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734266	TCGAAGCTTGCAAAA[C/G]TGAGACCCTGgagat	19013
rs16820265	snp	A/G	0.110727	0.207612	upstream-variant-2KB, intron-variant	Ppara	GRCm38.p3	15:85734201	gatgacctggattcc[A/G]acctggggactcaca	19013
rs16820266	snp	G/T	0.172336	0.23763	upstream-variant-2KB, intron-variant	Ppara	GRCm38.p3	15:85734040	GTATGATTTCCTGAA[G/T]GGCCCAGGGGATATT	19013
rs16820267	snp	A/G	0.244898	0.249948	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734627	AGGAGCGGCGTCCTG[A/G]GGNGTTGGCACCCCG	19013
rs16820268	snp	C/T	0.408163	0.193609	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734630	AGCGGCGTCCTGNGG[C/T]GTTGGCACCCCGGGG	19013
rs16820269	snp	A/G	0.188366	0.242283	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734675	GTGACTGAAGATCCA[A/G]GGNCGACACAAGCAA	19013
rs16820270	snp	A/G	0.244898	0.249948	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734678	ACTGAAGATCCANGG[A/G]CGACACAAGCAAAGN	19013
rs16820271	snp	A/C	0.090703	0.192677	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734693	NCGACACAAGCAAAG[A/C]GGCTGCTCTGGGTCG	19013
rs16820272	snp	A/G	0.444444	0.157135	upstream-variant-2KB, intron-variant	Ppara	GRCm38.p3	15:85734711	CTGCTCTGGGTCGCA[A/G]CCTGCTCCCAGTTGC	19013
rs16820273	snp	A/G	0.35124	0.228584	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734755	CGCTGTCAGTTGGCA[A/G]AGCCCCAGTGCCTNA	19013
rs16820274	snp	A/G	0.362812	0.2231	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734769	ANAGCCCCAGTGCCT[A/G]AGCTGGACACAGTCA	19013
rs16820275	snp	A/G	0.35124	0.228584	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734816	AGCGTATGCAGAGGG[A/G]CCACAGCCCGGGGCG	19013
rs16820276	snp	A/G	0.362812	0.2231	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734854	GGCGGAGGGTGGGTC[A/G]GAGCGGCCGCGCCTC	19013
rs16820277	snp	A/C	0.090703	0.192677	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734874	GGCCGCGCCTCCCTG[A/C]GACCGTCCTCGATGC	19013
rs16820278	snp	A/G	0.287335	0.247197	upstream-variant-2KB, utr-variant-5-prime, intron-variant	Ppara	Mm_Celera	15:85735002	TCATCCTGGGACTCT[A/G]AAGATCAGATTNCGC	19013
rs16820279	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85735771	CGGACTAGGGGCGCG[A/G]GTCTGGAGACCCACA	19013
rs16820280	snp	C/G	0.090703	0.192677	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85735830	GGCACACGCGTGCGA[C/G]TTTTCAGGGCCCNCG	19013
rs16820281	snp	A/G	0.090703	0.192677	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85735843	GANTTTTCAGGGCCC[A/G]CGGAACTGTCCGCCA	19013
rs16820282	snp	A/G	0.099723	0.199792	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85735955	TCCTGGAACTGGAGC[A/G]ACGCTGGGTCCTCTG	19013
rs16820283	snp	C/T	0.244898	0.249948	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85736000	GGGAGGGCACACGGG[C/T]GGGGACATCGGGGCG	19013
rs16820284	snp	A/T	0.0831758	0.186198	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85736049	GTGCATTTGGGCGTA[A/T]CTCACCGGGAGGCGT	19013
rs16820285	snp	C/T	0.15879	0.232768	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85736078	GTTTCCTGAGACCCT[C/T]GGGGAACTTAGAGGA	19013
rs16820286	snp	C/T	0.0831758	0.186198	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85736108	AGAGGTAACTGGAGG[C/T]TCCCTGACAGACTGA	19013
rs16820287	snp	C/T	0.0867769	0.189363	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85736171	CCTGAGAAACGCTGC[C/T]GGTGGGTTTGAGTCA	19013
rs16820288	snp	A/G	0.099723	0.199792	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85736231	TTCCTCATTGCTCCT[A/G]ATCGTAGTGGGGCGA	19013
rs16820289	snp	G/T	0.095	0.19615	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85736250	GTAGTGGGGCGATGT[G/T]GGCCCCAACAGTAGG	19013
rs16820290	snp	C/T	0.48	0.0979796	intron-variant	Ppara	Mm_Celera	15:85736755	CGGTTACAATATGTT[C/T]TNTGGATCTCCCCCA	19013
rs16820291	snp	C/T	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85736753	GTTACAATATGTTNT[C/T]TGGATCTCCCCCAAC	19013
rs16820292	snp	C/T	0.277778	0.248452	intron-variant	Ppara	Mm_Celera	15:85736736	GGATCTCCCCCAACT[C/T]TCCACCNCCTTGGGA	19013
rs16820293	snp	A/C	0.408163	0.193609	intron-variant	Ppara	Mm_Celera	15:85736729	CCCCAACTNTCCACC[A/C]CCTTGGGAAAGTCAC	19013
rs16820294	snp	C/T	0.117188	0.211804	intron-variant	Ppara	GRCm38.p3	15:85736658	CGCCCAAGAAAGTTC[C/T]GTGCTCCTCCCCCAA	19013
rs16820295	snp	A/G	0.260355	0.249785	intron-variant	Ppara	GRCm38.p3	15:85736409	TCCGGACTAGCACAC[A/G]GGCACTCCCGGCTCC	19013
rs16820296	snp	A/G	0.165289	0.235211	intron-variant	Ppara	GRCm38.p3	15:85737243	TGCTTCTTGGGGGCC[A/G]TCCCTGCCTGGCTAA	19013
rs16820297	snp	C/T	0.095	0.19615	intron-variant	Ppara	GRCm38.p3	15:85737214	AATGATGAAACTAAC[C/T]NACTACTTCATTGAA	19013
rs16820298	snp	A/G	0.104938	0.20361	intron-variant	Ppara	GRCm38.p3	15:85737213	ATGATGAAACTAACN[A/G]ACTACTTCATTGAAT	19013
rs16820299	in-del	-/C/CT/T	0.466759	0.178654	intron-variant	Ppara	Mm_Celera	15:85737114	AACGCAATACCACCT[-/C/CT/T]NTTTNAAACTACGCC	19013
rs16820301	in-del	-/T	0.391111	0.206368	intron-variant	Ppara	Mm_Celera	15:85737111	AATACCACCTNNTTT[-/T]AAACTACGCCGACGC	19013
rs16820302	snp	A/C	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85737083	CGCAGCCTGCCATAA[A/C]GAAATGNGGTTCCCA	19013
rs16820303	snp	C/T	0.35503	0.226867	intron-variant	Ppara	GRCm38.p3	15:85737076	TGCCATAANGAAATG[C/T]GGTTCCCATGAAGCA	19013
rs16820304	snp	C/T	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85736964	ACAAAATAACCACTA[C/T]CCAAGCCCTGTTGCT	19013
rs16820305	snp	G/T	0.0867769	0.189363	intron-variant	Ppara	GRCm38.p3	15:85736947	CAAGCCCTGTTGCTA[G/T]TCTGAAGTGCAACCA	19013
rs16820306	snp	A/G	0.4992	0.019984	intron-variant	Ppara	Mm_Celera	15:85777129	GGTTGCCAACTGCAC[A/G]GCAGCTTGGCACCTT	19013
rs16820307	snp	G/T	0.5	0	intron-variant	Ppara	Mm_Celera	15:85777264	tgcccacagaggtca[G/T]aagatcccctggaac	19013
rs16820308	snp	G/T	0.197531	0.244432	intron-variant	Ppara	Mm_Celera	15:85777304	agatgtttgtgagct[G/T]ccacgtaggtgttgg	19013
rs16820309	snp	A/G	0.0831758	0.186198	intron-variant	Ppara	Mm_Celera	15:85777367	agtactcccaactgc[A/G]gagtcatccctcnag	19013
rs16820310	snp	C/T	0.0831758	0.186198	intron-variant	Ppara	Mm_Celera	15:85777380	gcngagtcatccctc[C/T]agacccTGTTTGGAG	19013
rs16820311	snp	A/C	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85777455	GCTGCCACTGCTGAG[A/C]TTTGAGCTTAGACAG	19013
rs16820312	snp	A/G	0.493827	0.0552116	intron-variant	Ppara	GRCm38.p3	15:85777473	TGAGCTTAGACAGTG[A/G]TGNTTTCAATTNGNA	19013
rs16820313	snp	A/T	0.497323	0.0364873	intron-variant	Ppara	GRCm38.p3	15:85777476	GCTTAGACAGTGNTG[A/T]TTTCAATTNGNAACA	19013
rs16820314	snp	C/T	0.095	0.19615	intron-variant	Ppara	Mm_Celera	15:85777485	GTGNTGNTTTCAATT[C/T]GNAACAGNAAGTGAA	19013
rs16820315	snp	G/T	0.0831758	0.186198	intron-variant	Ppara	Mm_Celera	15:85777487	GNTGNTTTCAATTNG[G/T]AACAGNAAGTGAATG	19013
rs16820316	snp	A/G	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85777493	TTCAATTNGNAACAG[A/G]AAGTGAATGGCTATT	19013
rs16820317	snp	A/G	0.497041	0.0383476	intron-variant	Ppara	GRCm38.p3	15:85786758	tcaGAACACTTGTGG[A/G]TATGACTAGTCTATT	19013
rs16820318	snp	A/G	0.48	0.0979796	intron-variant	Ppara	GRCm38.p3	15:85786822	CTCTGTGTTGAGCCC[A/G]TGGCACGGGAGGCTG	19013
rs16820319	snp	A/G	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85786846	GAGGCTGGGGCCCCC[A/G]TGGAGGTCCTGTAAT	19013
rs16820320	snp	C/T	0.48	0.0979796	intron-variant	Ppara	GRCm38.p3	15:85786891	ACTGGAGATAGGGTA[C/T]GAGTCAGGAGACAGN	19013
rs16820321	snp	A/G	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85786906	NGAGTCAGGAGACAG[A/G]CTAGCANACGTGAGC	19013
rs16820322	snp	C/T	0.090703	0.192677	intron-variant	Ppara	Mm_Celera	15:85786913	GGAGACAGNCTAGCA[C/T]ACGTGAGCCTCAAGA	19013
rs16820323	snp	A/G	0.165289	0.235211	intron-variant	Ppara	Mm_Celera	15:85786943	AATGGTGGCACCATG[A/G]TAAGTAACCATGGGC	19013
rs16820324	snp	C/T	0.473373	0.11227	intron-variant	Ppara	GRCm38.p3	15:85787070	TGTCATGGGTGGTAA[C/T]ACCCCAGGTTTCACA	19013
rs16820325	snp	A/G	0.495317	0.04816	intron-variant	Ppara	GRCm38.p3	15:85787100	ATACTTTCCTCTTCC[A/G]TCTGTAGACACCCTC	19013
rs16820326	snp	C/T	0.0831758	0.186198	synonymous-codon	Ppara	Mm_Celera	15:85787136	AGCTTCCAGCCCTTC[C/T]TCAGTCAGCTGCCCN	19013
rs16820327	snp	C/T	0.0867769	0.189363	synonymous-codon	Ppara	Mm_Celera	15:85787151	NTCAGTCAGCTGCCC[C/T]GTGATCCCCGCCAGC	19013
rs16820328	snp	A/G	0.21875	0.248039	synonymous-codon	Ppara	GRCm38.p3	15:85789017	CCGATCACACTTGTC[A/G]TACACCAGCTTCAGC	19013
rs16820329	snp	A/G	0.095	0.19615	intron-variant	Ppara	GRCm38.p3	15:85788971	AAGAAGCCCTGTGAC[A/G]TCAACACATAATTTA	19013
rs16820330	snp	G/T	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85788920	GGTAAGCCTCCAGAC[G/T]GGCTTCNCGCAGCTT	19013
rs16820331	snp	A/G	0.099723	0.199792	intron-variant	Ppara	GRCm38.p3	15:85788913	CTCCAGACNGGCTTC[A/G]CGCAGCTTTCTCATG	19013
rs16820332	snp	C/T	0.0867769	0.189363	intron-variant	Ppara	GRCm38.p3	15:85788824	aagagcttgctctgg[C/T]ggccaaagangggct	19013
rs16820333	snp	C/T	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85788814	tctggnggccaaaga[C/T]gggcttgaactcttg	19013
rs16820334	snp	C/G	0.499314	0.0185058	intron-variant	Ppara	GRCm38.p3	15:85788712	TCTGAGGAGCCAACC[C/G]GGGGCTTCATGCATG	19013
rs16820335	snp	A/G	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85788711	ctgaggagccaaccn[A/G]gggcttcatgcatgc	19013
rs16820336	snp	C/T	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85788640	CCATCTCTAAGAAAC[C/T]ATGTGTTGAAGNTCT	19013
rs16820337	snp	C/T	0.0867769	0.189363	intron-variant	Ppara	GRCm38.p3	15:85788628	AACNATGTGTTGAAG[C/T]TCTAGAAAAGTCCCG	19013
rs16820338	snp	C/G	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85788611	CTAGAAAAGTCCCGT[C/G]TAACTGGGGCAAATA	19013
rs16820339	snp	A/G	0.0867769	0.189363	intron-variant	Ppara	GRCm38.p3	15:85788572	ATGTCTCTACATTGA[A/G]AANNGAAANTNATGT	19013
rs16820340	snp	C/T	0.491493	0.0646602	intron-variant	Ppara	GRCm38.p3	15:85788569	TCTCTACATTGAAAA[C/T]GGAAACTGATGTGCT	19013
rs16820341	snp	A/G	0.095	0.19615	intron-variant	Ppara	GRCm38.p3	15:85788568	CTCTACATTGANAAN[A/G]GAAANTNATGTGCTA	19013
rs16820342	snp	C/T	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85788563	CATTGANAANNGAAA[C/T]TNATGTGCTAAGGCA	19013
rs16820343	snp	A/G	0.172336	0.23763	intron-variant	Ppara	GRCm38.p3	15:85788561	TTGANAANNGAAANT[A/G]ATGTGCTAAGGCAGA	19013
rs16820344	snp	A/G	0.0867769	0.189363	intron-variant	Ppara	GRCm38.p3	15:85791050	CCAAGGGCAGTAGAA[A/G]CACCTACCGGGTTGT	19013
rs16820345	snp	A/G	0.0867769	0.189363	synonymous-codon	Ppara	GRCm38.p3	15:85791030	TACCGGGTTGTTGCT[A/G]GTCTTTCCCGCNAGT	19013
rs16820346	snp	A/G	0.095	0.19615	synonymous-codon	Ppara	GRCm38.p3	15:85791018	GCTNGTCTTTCCCGC[A/G]AGTATNACCCGGGCC	19013
rs16820347	snp	C/T	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85790787	TAGAAATGGTCAAGG[C/T]ANTCAAAAANCCAAG	19013
rs16820348	snp	C/T	0.345679	0.230967	intron-variant	Ppara	GRCm38.p3	15:85790785	GAAATGGTCAAGGNA[C/T]TCAAAAANCCAAGGC	19013
rs16820349	in-del	-/A	0.260355	0.249785	intron-variant	Ppara	Mm_Celera	15:85790777	CAAGGNANTCAAAAA[-/A]CCAAGGCAGAGGCAA	19013
rs16820350	snp	A/G	0.0867769	0.189363	intron-variant	Ppara	GRCm38.p3	15:85790737	GGTAGGTCACACTAG[A/G]AATGGCNAGCTAAAC	19013
rs16820351	snp	A/G	0.18	0.24	intron-variant	Ppara	GRCm38.p3	15:85790730	CACACTAGNAATGGC[A/G]AGCTAAACCAACCCA	19013
rs16820352	snp	A/G	0.090703	0.192677	intron-variant	Ppara	GRCm38.p3	15:85790706	CAACCCATTCCTCAT[A/G]ACCATCAAACTTTCT	19013
rs16820353	snp	C/T	0.244898	0.249948	intron-variant	Ppara	GRCm38.p3	15:85790679	TTCTACTACAGAGAC[C/T]GAAAACCAACTACAC	19013
rs16820354	snp	A/G	0.104938	0.20361	intron-variant	Ppara	Mm_Celera	15:85791280	CTAGGCATTATAAAG[A/G]CTGTGTAATTGATAC	19013
rs16820355	snp	A/G	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85791348	GGGTGTTTCTTAAGT[A/G]CGTTCTAATCCCTAT	19013
rs16820356	snp	C/T	0.107755	0.205588	intron-variant	Ppara	Mm_Celera	15:85791394	CAAACCTGTTGCTTC[C/T]CTACTCAGAACATTC	19013
rs16820357	snp	A/G	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85797768	ACAATTCTATGACAA[A/G]CTATGCAGTNCCCCT	19013
rs16820358	snp	C/T	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85797758	GACAANCTATGCAGT[C/T]CCCCTTAAACATCAA	19013
rs16820359	snp	A/C	0.090703	0.192677	intron-variant	Ppara	GRCm38.p3	15:85797713	CTACTGTGTCCCAAT[A/C]GCCAAGCTGGGTGGT	19013
rs16820360	snp	A/G	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85797695	CAAGCTGGGTGGTAG[A/G]ATGATTCCAAGTACN	19013
rs16820361	snp	A/G	0.090703	0.192677	intron-variant	Ppara	GRCm38.p3	15:85797680	NATGATTCCAAGTAC[A/G]NGTGCAGTGCAGTCC	19013
rs16820362	snp	C/T	0.090703	0.192677	intron-variant	Ppara	GRCm38.p3	15:85797679	ATGATTCCAAGTACN[C/T]GTGCAGTGCAGTCCC	19013
rs16820363	snp	A/G	0.090703	0.192677	intron-variant	Ppara	GRCm38.p3	15:85797652	TCCCATCCTTGGACA[A/G]TTTCAAACTCAGACA	19013
rs16820364	snp	A/G	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85797634	TCAAACTCAGACAAC[A/G]TAAGATTTTGCAGAA	19013
rs16820365	snp	A/G	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85797610	TGCAGAAAGCTAACA[A/G]TGTAAGTCAGTAAGA	19013
rs16820366	snp	A/G	0.090703	0.192677	intron-variant	Ppara	Mm_Celera	15:85797484	gtagctccaggccca[A/G]agaatgaaatgcctt	19013
rs16820367	snp	A/G	0.385633	0.210009	intron-variant	Ppara	GRCm38.p3	15:85797448	gacctgtgcagtacc[A/G]cacaggaaggaggag	19013
rs16820368	snp	G/T	0.197531	0.244432	synonymous-codon	Ppara	Mm_Celera	15:85798154	GAACCTGAGGAAGCC[G/T]TTCTGTGACATCATG	19013
rs16820369	snp	C/G	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85798638	AGAGTCTGGAAAGTA[C/G]AGTGCAGGTTTAGGT	19013
rs16820370	snp	C/T	0.0831758	0.186198	intron-variant	Ppara	Mm_Celera	15:85798667	GTGCAGTGCTATCCC[C/T]GTTAATACTGATGTT	19013
rs16820371	snp	C/T	0.260355	0.249785	splice-acceptor-variant, intron-variant	Ppara	Mm_Celera	15:85801010	GAAGGCCAGGCCGAT[C/T]TACGCTCAAAAGAAG	19013
rs16820372	snp	C/T	0.152778	0.230321	intron-variant	Ppara	GRCm38.p3	15:85800977	AAAGACGTCTGAGTG[C/T]GGCCATCGGAGAGGC	19013
rs16820373	snp	C/T	0.387812	0.208586	intron-variant	Ppara	GRCm38.p3	15:85800944	CAGTCAGTGGAGGAG[C/T]CAAGTGTCTGCTGCT	19013
rs16820374	snp	A/G	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85800941	TCAGTGGAGGAGCCA[A/G]GTGTCTGCTGCTTGG	19013
rs16820375	snp	C/T	0.120708	0.213971	intron-variant	Ppara	GRCm38.p3	15:85800935	GAGGAGNCANGTGTC[C/T]GCTGCTTGGTGTGGC	19013
rs16820376	snp	C/G	0.35503	0.226867	intron-variant	Ppara	Mm_Celera	15:85800916	GCTTGGTGTGGCCCC[C/G]CTGAGGAGGCACTGA	19013
rs16820377	snp	C/T	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85800891	GCACTGAGGGACCTT[C/T]NCAGGGCAGCCCNNN	19013
rs16820378	snp	A/C	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85800891	CACTGAGGGACCTTN[A/C]CAGGGCAGCCCNNNC	19013
rs16820379	snp	A/C/G	0.601562	0.10335	intron-variant	Ppara	GRCm38.p3	15:85800877	TTNNCAGGGCAGCCC[A/C/G]NNCGGGNCNGGAGGT	19013
rs16820381	snp	C/T	0.099723	0.199792	intron-variant	Ppara	Mm_Celera	15:85800877	NNCAGGGCAGCCCNN[C/T]CGGGNCNGGAGGTCA	19013
rs16820382	snp	C/T	0.117188	0.211804	intron-variant	Ppara	Mm_Celera	15:85800870	CAGCCCNNNCGGGNC[C/T]GGAGGTCACCGCCTC	19013
rs16820383	snp	C/T	0.197531	0.244432	intron-variant	Ppara	GRCm38.p3	15:85800841	TCTGATGGGTACAGA[C/T]ANGACTGACACTCCT	19013
rs16820384	snp	C/T	0.197531	0.244432	intron-variant	Ppara	GRCm38.p3	15:85800839	TGATGGGTACAGANA[C/T]GACTGACACTCCTAG	19013
rs16820385	snp	C/T	0.117188	0.211804	intron-variant	Ppara	GRCm38.p3	15:85800749	TACTTTTGGATTTGC[C/T]TGATAATCCCCAAAC	19013
rs16820386	snp	A/C	0.396694	0.202437	intron-variant	Ppara	Mm_Celera	15:85800732	GATAATCCCCAAACC[A/C]CNCCACATCTTTGGA	19013
rs16820387	snp	A/C	0.297521	0.245442	intron-variant	Ppara	Mm_Celera	15:85800730	TAATCCCCAAACCNC[A/C]CCACATCTTTGGAGG	19013
rs16820388	snp	C/T	0.231111	0.249285	intron-variant	Ppara	GRCm38.p3	15:85800656	GCATCCCATCAGCAG[C/T]AAGGGGCATGACAAA	19013
rs16820389	snp	A/G	0.099723	0.199792	utr-variant-3-prime, missense	Ppara	Mm_Celera	15:85801273	ATCTTTCCTGAGATG[A/G]CAGGCCNTTNCCACT	19013
rs16820390	snp	A/G	0.099723	0.199792	utr-variant-3-prime, missense	Ppara	Mm_Celera	15:85801280	CTGAGATGNCAGGCC[A/G]TTNCCACTGTTCAGG	19013
rs16820391	snp	A/G	0.465374	0.126941	utr-variant-3-prime, missense	Ppara	GRCm38.p3	15:85801283	AGATGNCAGGCCNTT[A/G]CCACTGTTCAGGGAC	19013
rs16820392	snp	A/G	0.413194	0.189387	utr-variant-3-prime, missense	Ppara	GRCm38.p3	15:85801312	ACCTCCGAGGCCTGC[A/G]GCCCCATACAGGAGA	19013
rs16820393	snp	C/T	0.156735	0.231952	utr-variant-3-prime	Ppara	Mm_Celera	15:85801402	GGTAATGCGGGCTCT[C/T]CCCACATCCTTNNNN	19013
rs16820407	snp	C/G	0.095	0.19615	utr-variant-3-prime	Ppara	Mm_Celera	15:85801447	NNNNNACCTGCTACC[C/G]AAATGGGGGTGATCG	19013
rs16820408	snp	C/T	0.33241	0.236027	utr-variant-3-prime	Ppara	GRCm38.p3	15:85801495	GACAGTGACAGACAA[C/T]GGCAGTCCCCAGTCT	19013
rs16820409	snp	A/G	0.095	0.19615	utr-variant-3-prime	Ppara	Mm_Celera	15:85801569	TTGCGTTTATAATTC[A/G]CCATTAATTAACGGG	19013
rs16820410	snp	A/G	0.482104	0.0928863	utr-variant-3-prime	Ppara	Mm_Celera	15:85801592	TTAACGGGTAACCTC[A/G]AAGTCTGAGCGGNCT	19013
rs16820411	snp	G/T	0.107755	0.205588	utr-variant-3-prime	Ppara	Mm_Celera	15:85801605	TCNAAGTCTGAGCGG[G/T]CTGTTCCCTTCCTGC	19013
rs16820412	snp	A/C	0.48	0.0979796	utr-variant-3-prime	Ppara	Mm_Celera	15:85801721	GGCCCAAGGTTAGCC[A/C]TTTAAATGTGGCAAA	19013
rs16820413	snp	A/G	0.426035	0.177515	utr-variant-3-prime	Ppara	Mm_Celera	15:85801762	AATGTTTATTGGGAA[A/G]ACTTCACTTGAGTTT	19013
rs16820414	snp	A/G	0.152778	0.230321	utr-variant-3-prime	Ppara	Mm_Celera	15:85801819	TCTGAGAACATTCGA[A/G]AANAGTTTGATAAGC	19013
rs16820415	snp	A/T	0.117188	0.211804	utr-variant-3-prime	Ppara	Mm_Celera	15:85801822	GAGAACATTCGANAA[A/T]AGTTTGATAAGCTAT	19013
rs16820416	snp	C/T	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85801867	TGGGGGCTCACTGTT[C/T]TGGAGGGNGTAACTG	19013
rs16820417	snp	G/T	0.489796	0.070696	utr-variant-3-prime	Ppara	Mm_Celera	15:85801875	CACTGTTNTGGAGGG[G/T]GTAACTGACTCATGA	19013
rs16820418	snp	A/G	0.297521	0.245442	utr-variant-3-prime	Ppara	Mm_Celera	15:85801932	TTTCAGATTTGTGTA[A/G]AAGATTCCCAGAAAG	19013
rs16820419	snp	C/T	0.345679	0.230967	utr-variant-3-prime	Ppara	Mm_Celera	15:85801954	CCCAGAAAGTTACAT[C/T]TTCAAGAAGCCCTCA	19013
rs16820420	snp	C/T	0.408163	0.193609	utr-variant-3-prime	Ppara	Mm_Celera	15:85802027	CCTGAGCAGGTAGTT[C/T]TGCACNTCTGTTCAT	19013
rs16820421	snp	C/T	0.104938	0.20361	utr-variant-3-prime	Ppara	Mm_Celera	15:85802033	CAGGTAGTTNTGCAC[C/T]TCTGTTCATGTCANA	19013
rs16820422	snp	G/T	0.489796	0.070696	utr-variant-3-prime	Ppara	Mm_Celera	15:85802058	GTCANACCCTCAGGG[G/T]GNGGGCATGGCAGCA	19013
rs16820423	snp	G/T	0.489796	0.070696	utr-variant-3-prime	Ppara	Mm_Celera	15:85802060	CANACCCTCAGGGNG[G/T]GGGCATGGCAGCAAT	19013
rs30531529	snp	C/T	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85800402	CTCTGGTCATCTCTC[C/T]GCCTGCTTTCCACCT	19013
rs31557255	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85752817	AACTGTGGGCATGTC[C/T]GAGAGATTGATTGTC	19013
rs31560309	snp	A/C	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85745352	GTGTGTGTGGTATGT[A/C]TGTTCCCATGTAAAC	19013
rs31561215	snp	C/G	0.207612	0.24638	intron-variant	Ppara	Mm_Celera	15:85741507	ACTTTTTTGAAACTA[C/G]GAAACCTGAGGATCT	19013
rs31573845	snp	G/T	0.48	0.0979796	intron-variant	Ppara	Mm_Celera	15:85777176	AGAAATTTAAAAATA[G/T]ATATTAATTTTATTT	19013
rs31584724	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85783151	TGGTTCCAAGTTACA[A/G]CCCATCACAGCAGTG	19013
rs31584947	snp	C/G	0.484429	0.0868505	intron-variant	Ppara	GRCm38.p3	15:85772644	CCTCTGTTAATAATA[C/G]AGAGGTTTGGCGATG	19013
rs31588595	snp	A/G	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85752869	AGGGTCCAGCCCACC[A/G]TGGGTGGTACCATCC	19013
rs31588864	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85761691	CAATGTATCTGCATC[C/T]GGATAGACAATAATA	19013
rs31599542	snp	G/T	0.188366	0.242283	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85774199	ATCCCCATGTGCTTT[G/T]ACCCTTTCCCACCAT	19013
rs31627256	snp	A/G	0.375	0.216506	upstream-variant-2KB	Ppara	Mm_Celera	15:85726800	TCAGCTACCCCTCCA[A/G]CTCCATGTCTGCCTG	19013
rs31635296	snp	G/T	0.497778	0.0332592	intron-variant	Ppara	GRCm38.p3	15:85754208	AAGAAAGGCTTTGCC[G/T]TGCAGTCTGCCCTGT	19013
rs31638105	snp	G/T	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85765249	CTTCCTGACGCGTGC[G/T]ACAGGACCATTGCAC	19013
rs31640195	snp	G/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85752547	CACCTTAGTAACAGG[G/T]GGATTGGTCAGAACT	19013
rs31652682	snp	C/T	0.265928	0.249492	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85777044	GCCTGTTCTAGGGAA[C/T]GTGGACTTTGCTCTT	19013
rs31653175	snp	A/T	0.117188	0.211804	intron-variant	Ppara	Mm_Celera	15:85747632	AGTCTCTGTAGTACT[A/T]TTCTTCTGAGGTACC	19013
rs31660559	snp	C/T	0.231111	0.249285	intron-variant	Ppara	Mm_Celera	15:85754237	GTCCTTTCAACACTG[C/T]TGTTATCTGTGGGCA	19013
rs31677041	snp	A/G	0.375	0.216506	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85776026	GCTGGGATTAAAGGC[A/G]TGCACCACTCATTTC	19013
rs31685131	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85783147	GTTATGGTTCCAAGT[C/T]ACAACCCATCACAGC	19013
rs31685620	snp	A/G/T	0.32	0.24	upstream-variant-2KB	Ppara	GRCm38.p3	15:85726378	TACACCCAAGGTACC[A/G/T]CGAGGAAGAACCACC	19013
rs31686915	snp	A/G	0.197531	0.244432	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Ppara	Mm_Celera	15:85771881	CCTTCAGCGTTGTTG[A/G]GCAAGAACCAGGTGA	19013
rs31689155	snp	C/T	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85792017	GGGTTCCTCAGGTCG[C/T]GGTGATCCCCCCCCA	19013
rs31708044	snp	C/T	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85803011	CCTCAAACCCACTTG[C/T]CCCCTTTGTCTTCCC	19013
rs31708589	snp	G/T	0.48	0.0979796	intron-variant	Ppara	GRCm38.p3	15:85744820	CACTTACTGCCCCCA[G/T]TGAGGCTGATCTGGG	19013
rs31717376	snp	A/G	0.484429	0.0868505	utr-variant-3-prime, intron-variant, downstream-variant-500B	Ppara, Cdpf1	GRCm38.p3	15:85806562	TATCCAGGACATCAG[A/G]AATCAGGGTGAACAC	19013
rs31718912	snp	A/G	0.290657	0.246672	utr-variant-3-prime	Ppara	Mm_Celera	15:85805664	TACCTCACAACAGAC[A/G]AACGCCACTTGGCAC	19013
rs31724299	snp	A/G	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85804231	TATGTCATGGGGTAT[A/G]TTAGACACTCAGCAG	19013
rs31736498	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85739508	GCCTTTTTAATGCAC[C/T]GAGCAAGCTAGAATG	19013
rs31737725	snp	A/G	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85803322	AGTTTTGAGTCATGG[A/G]CTTTCGGGATAGTTG	19013
rs31742982	snp	C/T	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85754790	GTTTCATCAGTGGGT[C/T]ACAAACACAAAACCC	19013
rs31746606	snp	C/G	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85786654	TCTCTGTCTCTGACT[C/G]GGTCTCTGTCTCACT	19013
rs31753418	snp	C/G	0.290657	0.246672	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85775799	ATTCCAAGCTCCAGA[C/G]GTGAATTTCACAGAA	19013
rs31756699	snp	A/C	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85748034	CTCCAAGCTAGCTGG[A/C]CTGAGAGCTATCCAG	19013
rs31761521	snp	C/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85764287	AAAAGTTTGTTTTTC[C/T]TTTTAGGAAATAATA	19013
rs31763260	snp	C/T	0.277778	0.248452	utr-variant-3-prime	Ppara	Mm_Celera	15:85804781	TAAGTGGACCACGTT[C/T]CTCACCGAGACTCCT	19013
rs31765956	snp	C/T	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85779523	TTTTTACATACACAT[C/T]AAAGTTCCTTTCTCT	19013
rs31769263	snp	A/G/T	0.207612	0.24638	intron-variant	Ppara	GRCm38.p3	15:85744448	GGTGGTTGAAAACCC[A/G/T]ACCTGGAGAGATGGT	19013
rs31772214	snp	C/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85783419	GTGGGAATTGAACTC[C/T]AGTCCTCTGGAAGAG	19013
rs31773124	snp	A/G	0.345679	0.230967	intron-variant	Ppara	Mm_Celera	15:85799013	TTGTCACATTGTCAC[A/G]CTCCCGAAAAGCGTA	19013
rs31777353	snp	A/G	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85761514	GTAGAAGATCATAAC[A/G]CGCTCCCGAATCCCT	19013
rs31778750	snp	C/T	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85746774	GAGCTAAACTCCTCT[C/T]GACCCACATCGGCCG	19013
rs31783013	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85783587	TTATTCTGTAGGTAT[A/G]CCATGTTTCCTTTCT	19013
rs31783985	snp	A/G	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85741551	TGTGTATATATATAT[A/G]TGTGTGTGTGTGTGT	19013
rs31786461	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85739752	TTGCTTCCCTCCCAC[C/T]CTGCCCCCCCAAAAC	19013
rs31791603	snp	C/G	0.495868	0.0452663	intron-variant	Ppara	Mm_Celera	15:85761747	CATATTTTTCTAACA[C/G]TCAAATTGAAATCTA	19013
rs31802185	snp	G/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85740849	TAGTGATCAATGGGG[G/T]AGGGCCCAGCCCCTT	19013
rs31808118	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85730226	GCCAGAAGACCCTTC[C/T]GCAGAGTGCTATGGA	19013
rs31811452	snp	A/C	0.375	0.216506	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85776272	CGCTCCCTCCTCCTG[A/C]CCCCTCCCCCTAGTC	19013
rs31831905	snp	A/T	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85760595	TAATTCCAGACTCTG[A/T]GGAAACAGGGAATTC	19013
rs31832101	snp	C/T	0.207612	0.24638	intron-variant	Ppara	Mm_Celera	15:85742338	CCTAGTAATGAGAGG[C/T]GGATGGGTGGACGCG	19013
rs31835952	snp	A/G	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85768523	CCAGGAAGCAGGAGC[A/G]GGTGGATTTCTGTGA	19013
rs31844442	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85739632	GTTGTTGAACATCGA[A/G]CCTGGGACTTGAAGT	19013
rs31846037	snp	G/T	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85804227	ACACTATGTCATGGG[G/T]TATATTAGACACTCA	19013
rs31848401	snp	A/G	0.48	0.0979796	intron-variant	Ppara	Mm_Celera	15:85792011	AATACAGGGTTCCTC[A/G]GGTCGTGGTGATCCC	19013
rs31856428	snp	C/T	0.5	0	intron-variant	Ppara	Mm_Celera	15:85793389	TCCTGCCTCAGCCTT[C/T]TGAGGACTAGGATAA	19013
rs31863250	snp	C/G	0.48	0.0979796	upstream-variant-2KB	Ppara	Mm_Celera	15:85726369	ACCCAAAACTACACC[C/G]AAGGTACCTCGAGGA	19013
rs31864476	snp	A/G	0.207612	0.24638	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85776738	CATTTATTTTCTAAA[A/G]CCATCTACTATACCC	19013
rs31871407	snp	C/T	0.290657	0.246672	intron-variant	Ppara	Mm_Celera	15:85742425	CGAAGCAAGATGCCT[C/T]GTAAAAAACCGAAGA	19013
rs31890357	snp	A/T	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85729670	CATGGGGTTGTTAGC[A/T]CTCGGTGAGGCCAAG	19013
rs31893534	snp	C/G	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85740977	TTTCCTCTCCAACTT[C/G]CTTTTTGGTCATGGT	19013
rs31894256	snp	A/G	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85792016	AGGGTTCCTCAGGTC[A/G]TGGTGATCCCCCCCC	19013
rs31898267	snp	C/T	0.375	0.216506	utr-variant-3-prime	Ppara	GRCm38.p3	15:85803998	GCAAAATTTAGTCAT[C/T]GACTGGACTAAGGTC	19013
rs31906473	snp	C/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85746243	CAGGCACATTCCTGC[C/T]GAGCCTTCTCCCCAA	19013
rs31917499	snp	A/T	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85789883	GAAGACCCTGTCTTT[A/T]AAAAAAAAAATTAGT	19013
rs31919255	snp	A/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85778095	CCATCCTTCCTACTC[A/T]CCACGTAACTTCTGG	19013
rs31922889	snp	A/G	0.475309	0.108333	intron-variant, utr-variant-5-prime	Ppara	GRCm38.p3	15:85772258	AGTGAGTCCGGAGCC[A/G]CCTGCTGGCAACTTG	19013
rs31925324	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85783163	ACAACCCATCACAGC[A/G]GTGATGTCGGCAAGA	19013
rs31929562	snp	C/T	0.5	0	upstream-variant-2KB	Ppara	Mm_Celera	15:85726307	CAGTCTCATGGAACC[C/T]CAGCAAAGACTGGCT	19013
rs31933053	snp	A/G	0.5	0	intron-variant	Ppara	Mm_Celera	15:85794814	TGTGTGCGTGCATGC[A/G]TGTGCATGAGAGAGG	19013
rs31933867	snp	C/T	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85791979	GGTTTTCACCCTTCC[C/T]AGTGCTGCGATCCTT	19013
rs31948695	snp	C/G	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85768869	GCAAGGACACGCCAC[C/G]ACACAGAGCTCTTTA	19013
rs31962159	snp	C/T	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85760666	CTCTTTGAGAGAGCC[C/T]ACCTGGATCAATAAG	19013
rs31964040	snp	A/G	0.493827	0.0552116	intron-variant	Ppara	GRCm38.p3	15:85769301	TCTCTGGTTTACAGC[A/G]GTGTTGTGTCTGACA	19013
rs31965221	snp	A/G	0.5	0	intron-variant	Ppara	Mm_Celera	15:85741603	TGTGTGTGTGTGTGT[A/G]TGTAAAATTTCAAGA	19013
rs31966053	snp	A/C	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85753072	CTTAATGTTTATCAC[A/C]GTAACAGAAAAGCAA	19013
rs31971364	snp	A/G	0.290657	0.246672	intron-variant	Ppara	Mm_Celera	15:85755057	GCTGGGCTCATGCAA[A/G]GAGCAACAAGGCAGT	19013
rs31973194	snp	A/G	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85762062	AGGCATCCATGTGGT[A/G]TATATATATATATAT	19013
rs31988784	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85745275	TGTGTGAATGCACTC[A/G]TATGTGCGTGTGTGT	19013
rs31995919	snp	C/T	0.375	0.216506	upstream-variant-2KB	Ppara	Mm_Celera	15:85726286	ATTCTTAGAAGGAGC[C/T]TCATTCAGTCTCATG	19013
rs31998520	snp	G/T	0.444444	0.157135	utr-variant-3-prime	Ppara	Mm_Celera	15:85804437	CCTTTCAAGAGGAGT[G/T]TCCACTGGGAAAATC	19013
rs32002813	snp	C/T	0.46875	0.121031	intron-variant	Ppara	GRCm38.p3	15:85789443	CATTCATCCATTTAG[C/T]TTTTGAGATGGGGAC	19013
rs32012636	snp	C/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85767917	TCACATGTGTGTATG[C/T]TTCCGAATGCTTCTC	19013
rs32029135	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85789208	TTGTGATTGGGTGTG[C/T]TGTGCTGTGTAACTA	19013
rs32035672	snp	G/T	0.444444	0.157135	utr-variant-3-prime	Ppara	Mm_Celera	15:85805056	TTTAGTTAGGGGGGG[G/T]GGGTGGTTGAATCGT	19013
rs32039308	snp	A/G	0.32	0.24	utr-variant-3-prime	Ppara	Mm_Celera	15:85802547	TCCAAGGGGGTGGCT[A/G]CATATTTCAGAGCAG	19013
rs32056655	snp	C/T	0.48	0.0979796	intron-variant	Ppara	Mm_Celera	15:85730031	TCAATACATCTTTTC[C/T]CTCCAGTTTGCTGAG	19013
rs32073279	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85730472	GACCAGCTTCAGCCA[C/T]GAGATGGAAGCCAAG	19013
rs32083909	snp	A/G	0.444444	0.157135	utr-variant-3-prime	Ppara	Mm_Celera	15:85805182	TGACACCTTAGTGGC[A/G]ATCAAGTACTACTGT	19013
rs32090859	snp	C/T	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85806086	CAAGTGCCAGCCAGG[C/T]TTGACTGAACCATGA	19013
rs32097580	snp	G/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85737680	GAAAGCATGTTTCTA[G/T]TTTGTTTTATTAACT	19013
rs32098928	snp	A/G	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85782690	ACTGGTGGTGGCGGC[A/G]GCCACAATTGTACTT	19013
rs32106970	snp	A/G	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85760500	AATTCAGTGTTAAAG[A/G]ATGTACTCTATGCGC	19013
rs32109011	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85777997	CCTGGTCTACAGAGT[A/G]AGTTCCAGGACAGCC	19013
rs32109544	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85777959	GGAGGCAGAGGCAGG[C/T]GGATTTTTGAGTTCG	19013
rs32116386	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85760909	TATATATATGTGTGT[A/G]TATAGATATATGTTT	19013
rs32119154	snp	C/T	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85803281	AATCTTAGACAAATG[C/T]CACTCGTAGGTGACC	19013
rs32128763	snp	A/T	0.265928	0.249492	utr-variant-3-prime	Ppara	Mm_Celera	15:85803141	TGATCCTGGTGAGGG[A/T]TGAGCTCAGTCAGGA	19013
rs32128916	snp	C/T	0.290657	0.246672	intron-variant	Ppara	Mm_Celera	15:85742244	CCCTCTGGCCTTTGA[C/T]AGCCATCTGTAACTG	19013
rs32131993	snp	A/G	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85786023	TAGTTTAATCGGTAC[A/G]CAGTGATAGTCTCTG	19013
rs32135725	snp	C/T	0.304688	0.243945	utr-variant-3-prime	Ppara	Mm_Celera	15:85804742	AAAAACACTAAAATC[C/T]GCATGGAGAGGTTTT	19013
rs32149558	snp	A/G	0.48	0.0979796	upstream-variant-2KB	Ppara	Mm_Celera	15:85726370	CCCAAAACTACACCC[A/G]AGGTACCTCGAGGAA	19013
rs32155299	snp	A/C	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85803252	CCCTAGGAGGACAGG[A/C]TCCTGTTCTGGTGAA	19013
rs32160940	snp	C/T	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85742350	AGGTGGATGGGTGGA[C/T]GCGCCCAATTCTGAA	19013
rs32163852	snp	A/G	0.444444	0.157135	utr-variant-3-prime	Ppara	Mm_Celera	15:85805609	AAAAAAAAAAAAGGC[A/G]GGGCCCAGCCAGCTC	19013
rs32165814	snp	A/G	0.375	0.216506	upstream-variant-2KB	Ppara	Mm_Celera	15:85726588	GGCCCAGCACATGGT[A/G]TATCTCAGCTTCTGT	19013
rs32173225	snp	C/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85767723	TGCAGCTCATGACTG[C/T]CCATAACTCCAGTCC	19013
rs32175746	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85737592	GTATCAATGTGTGTT[C/T]GTATGTGTGTATGTG	19013
rs32184954	snp	C/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85788271	GGCTAGAGGAAGAAG[C/T]AAAAGCAAAGAACCC	19013
rs32187729	snp	A/G	0.48	0.0979796	intron-variant	Ppara	GRCm38.p3	15:85746366	CTTGTTCCTAGGCTC[A/G]TTTATTTATTCAACA	19013
rs32188799	snp	A/G	0.290657	0.246672	utr-variant-3-prime	Ppara	Mm_Celera	15:85806111	CCATGACTGGAAACC[A/G]TCAACTTTACATCAG	19013
rs32194132	snp	C/T	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85761515	TAGAAGATCATAACA[C/T]GCTCCCGAATCCCTT	19013
rs32203598	snp	A/C	0.375	0.216506	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85776243	CCCCTCCTCCTGCCC[A/C]CCCCCACCACAGCCG	19013
rs32204672	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85739768	CTGCCCCCCCAAAAC[A/G]TTTTTGCTTCGTATG	19013
rs32211444	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85782985	CCTGTTGAACGTATG[C/T]GTAGGAAGCTATCCC	19013
rs32230702	snp	A/G	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85788352	GGGATGGGGCCCTCC[A/G]TCAAGGCCATGTCTA	19013
rs32237974	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85731175	ATAGTGTTTAATTTA[C/T]ATAGCAGGCACACAA	19013
rs32252035	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85791470	TGCTTTTTCTTCAGT[A/G]TGATAGCTCAGGTCT	19013
rs32253435	snp	A/G	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85752264	TGTAAAGGAAAGGCC[A/G]AGAGTATGGAGCCAA	19013
rs32264004	snp	C/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85778156	GTTTCCCAGAACTTC[C/G]TCTAAACGGCACAGT	19013
rs32266396	snp	A/C	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85753029	CTTGGAAGTGGTGAA[A/C]CTTTTTCTCTCTTAG	19013
rs32272190	snp	A/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85760883	TGTATATATATATAG[A/T]TGTGTATACGTATAT	19013
rs32300076	snp	C/T	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85768683	TGTGTTGTGTACACA[C/T]ACATACTAACACACA	19013
rs32300145	snp	A/G	0.265928	0.249492	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Ppara	Mm_Celera	15:85772059	ATCACTGTGTGGTTG[A/G]TAATGATTAACCTAT	19013
rs32302447	snp	A/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85730202	TGAGCTCTGCAGATG[A/T]GCTACAGGGCCAGAA	19013
rs32303278	snp	A/G	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85804357	ATTAACCAGCCTTTG[A/G]CCCCAGGGCCTCCTA	19013
rs32306400	snp	A/G	0.492188	0.0620098	intron-variant	Ppara	GRCm38.p3	15:85752154	GTCCCTTCCGACAGC[A/G]TTGTGGCCAGTAGCA	19013
rs32309692	snp	C/G	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85760132	TTCTGTTGTGATTTC[C/G]ATATGGCATGTCTTC	19013
rs32310101	snp	A/G	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85804866	TGGCTCATCAGGAAA[A/G]GATGTGTGGTCCCTA	19013
rs32314675	snp	A/C	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85752522	TAACAGATTTGTCTC[A/C]TCAATGCAACACCTT	19013
rs32320740	snp	A/G	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85804021	CTAAGGTCTATCATG[A/G]CCTCCCTTTTGATCC	19013
rs32321326	snp	A/C	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85792033	TCGTGGTGATCCCCC[A/C]CCAACCATAAAATTA	19013
rs32324421	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85783515	GATCCCCTGTGTAGG[A/G]CATGGTGCTGCCCAC	19013
rs32329404	snp	C/T	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85740797	GAGCCTTAGTTGAGG[C/T]AATGCTTCCTTCAGA	19013
rs32336557	snp	A/G	0.345679	0.230967	utr-variant-3-prime	Ppara	Mm_Celera	15:85802309	TGGAGAACAAGAGAC[A/G]AGGGTGTGATTTCAT	19013
rs32341061	snp	C/T	0.48	0.0979796	intron-variant	Ppara	GRCm38.p3	15:85769222	TCAGGGTGTGGCCCA[C/T]GATAAGCGCTCAGGA	19013
rs32345608	snp	A/G	0.487535	0.077957	intron-variant	Ppara	Mm_Celera	15:85747224	GCAGTAGGGCTGGTC[A/G]TGGATGTTTCTGGAC	19013
rs32350455	snp	C/T	0.265928	0.249492	utr-variant-3-prime	Ppara	Mm_Celera	15:85804115	CTTCCCCAGAAAAGA[C/T]TGCTTGAAGCAGACC	19013
rs32362975	snp	A/G	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85752443	TCAGCCCTACAAAGA[A/G]TGATCTCCAATGGTA	19013
rs32373732	snp	G/T	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85760612	GAAACAGGGAATTCC[G/T]AGAATGAAATGGCTA	19013
rs32377774	snp	A/G	0.444444	0.157135	utr-variant-3-prime	Ppara	Mm_Celera	15:85804872	ATCAGGAAAGGATGT[A/G]TGGTCCCTAATCAGG	19013
rs32386466	snp	C/T	0.408163	0.193609	intron-variant	Ppara	Mm_Celera	15:85793235	ATTTAAAACATTTAT[C/T]TTGTGCATATGTGCA	19013
rs32389654	snp	A/C	0.5	0	intron-variant	Ppara	Mm_Celera	15:85793324	AGAGACAGAGACACA[A/C]AGAGAGAATGTCTCA	19013
rs32394174	snp	A/C/G	0.42	0.183303	intron-variant	Ppara	GRCm38.p3	15:85787673	CCATGTGTTGAGCAA[A/C/G]GGTGTTCTGTCCCTA	19013
rs32397767	snp	C/T	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85782741	GCACACACTGGCCAG[C/T]ATCTCTCCTTCTTTG	19013
rs32400154	snp	G/T	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85729932	AGCAAAACAAAGGGG[G/T]ATTTACAACAATAAC	19013
rs32414658	snp	C/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85764547	ACAGGACACACATTA[C/T]TTGTCAAGTTGCCTA	19013
rs32416656	snp	A/C	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85761025	AAGAAAGAAGTTATC[A/C]TGAGCTGAGTCGTGT	19013
rs32426013	snp	C/G	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85761295	AGACCATCGATCTAT[C/G]GATCTACCACAGGTG	19013
rs32428285	snp	A/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85752285	ATGGAGCCAATAAAA[A/T]CAGTGGTGGTCTGGA	19013
rs32430421	snp	A/T	0.33241	0.236027	intron-variant	Ppara	Mm_Celera	15:85791767	TTTCCTCATTTGGAA[A/T]TACAAGCTAGAATTT	19013
rs32433824	snp	A/G	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85762107	TATATATATATGTGT[A/G]TGTGTGTGTGTGTGT	19013
rs32436300	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85760853	TGTGTACATATATCT[A/G]TGTATGTATATGTGT	19013
rs32442613	snp	C/T	0.5	0	upstream-variant-2KB	Ppara	Mm_Celera	15:85727234	TTGCTGGGATTTGAA[C/T]TCAGGACCTTCGGAA	19013
rs32457386	snp	A/C	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85730235	CCCTTCCGCAGAGTG[A/C]TATGGAGCCTGGGGC	19013
rs32462046	snp	A/G	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85754795	ATCAGTGGGTTACAA[A/G]CACAAAACCCCATCT	19013
rs32478617	snp	A/T	0.48	0.0979796	intron-variant	Ppara	GRCm38.p3	15:85742346	TGAGAGGTGGATGGG[A/T]GGACGCGCCCAATTC	19013
rs32480328	snp	A/G	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85762101	TATATATATATATAT[A/G]TGTGTATGTGTGTGT	19013
rs32480602	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85730443	AACTATGTGGAAGGA[A/G]GGCCTGGAATGGAGA	19013
rs32483346	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85783112	TGACAAAGCCACTGA[A/G]GGGAGAATGTATTGT	19013
rs32484873	snp	A/C	0.5	0	intron-variant	Ppara	Mm_Celera	15:85730459	GGCCTGGAATGGAGA[A/C]CAGCTTCAGCCATGA	19013
rs32501171	snp	C/T	0.197531	0.244432	utr-variant-3-prime	Ppara	Mm_Celera	15:85805997	CCTCACCTGTCACTG[C/T]CCCTAAGCTGTGTAC	19013
rs32504661	snp	A/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85731221	CAACTAGAATAACTG[A/T]AATAATACGCTGCAA	19013
rs32512960	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85739375	TCTACATAGTGAGTT[C/T]CAGGCCAACCAGGGC	19013
rs32520651	snp	C/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85764576	TAATTCGCTGATATG[C/T]ACCATATTTTGAGTC	19013
rs32529018	snp	G/T	0.5	0	upstream-variant-2KB	Ppara	Mm_Celera	15:85727200	ATCTTGTTATGGATG[G/T]TTGTGAGCCACCATG	19013
rs32541261	snp	A/T	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85806103	TGACTGAACCATGAC[A/T]GGAAACCATCAACTT	19013
rs33858527	snp	A/G	0.46875	0.121031	utr-variant-3-prime	Ppara	Mm_Celera	15:85802896	AGAATAATAATAAGG[A/G]AAAATTAGCATTGGG	19013
rs33858776	snp	C/T	0.32	0.24	intron-variant	Ppara	GRCm38.p3	15:85769229	GTGGCCCACGATAAG[C/T]GCTCAGGAGTGTTAG	19013
rs33858934	snp	C/T	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85752040	AGTAGAAAGAGTCCC[C/T]GAGTCTCTTGCTGGA	19013
rs33858949	snp	C/G	0.5	0	intron-variant	Ppara	Mm_Celera	15:85793296	AGAGAGAGAGAGAGA[C/G]AGAGACAGAGACAGA	19013
rs33885747	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85777983	GAGTTCGAGGCCAGC[C/T]TGGTCTACAGAGTAA	19013
rs36243057	snp	C/T	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85773286	GTTGAAACTTCTGCA[C/T]TATCCTGTGGCACAC	19013
rs36251815	snp	A/G	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85798915	GGCATAGACCTATGG[A/G]TGACAGTTCTACCTA	19013
rs36253764	snp	C/T	0.48	0.0979796	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770114	TGTCATGGGTGTCAC[C/T]GCTTCTGCCAGTTAC	19013
rs36260283	snp	A/G	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85768385	GACCATAATCACACA[A/G]CATTCAGCAGCATGA	19013
rs36282236	snp	C/T	0.18	0.24	intron-variant	Ppara	Mm_Celera	15:85752147	TGAAGAAGTCCCTTC[C/T]GACAGCATTGTGGCC	19013
rs36285248	snp	A/G	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85796910	CATGGTACTGCATCG[A/G]AAAGGGAGCCCGGCT	19013
rs36292757	snp	C/T	0.124444	0.216185	utr-variant-3-prime, intron-variant, downstream-variant-500B	Ppara, Cdpf1	Mm_Celera	15:85806716	AACTGACTGTACGAG[C/T]GATTTATATCCTGAA	19013
rs36303136	snp	A/G	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85757426	CCATTCATGGCAAGC[A/G]TGCAATTTATAGTAC	19013
rs36310984	snp	C/T	0.444444	0.157135	utr-variant-3-prime	Ppara	Mm_Celera	15:85805140	CCAGGGTCAGCGTCA[C/T]GTCTTGACCAAGCAG	19013
rs36313409	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85769835	CAAGGCTTCCTTCTC[C/T]GAGGAATTTTCTTGA	19013
rs36316876	snp	C/T	0.231111	0.249285	intron-variant	Ppara	Mm_Celera	15:85797315	GCAGCCTCTTTGTTT[C/T]TTAGTATTGCAATCC	19013
rs36319443	snp	A/G	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85748963	CCATGATTCCTGGCC[A/G]GTTTCAAAGTCACTC	19013
rs36319976	snp	C/T	0.495868	0.0452663	intron-variant	Ppara	GRCm38.p3	15:85796174	ACTCCTCATGAAACT[C/T]GTAAGGTATCTGGAG	19013
rs36324826	snp	A/G	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85763209	AGGTCCAGAAACTGT[A/G]CCTACAACTCCTACT	19013
rs36324905	snp	C/T	0.132653	0.220748	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85775701	CCATCTCCTCAGTCC[C/T]GGGATGATTTTGTCT	19013
rs36350778	snp	C/T	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85740350	CTGGGACACCTGTGT[C/T]TCACCTACCGCAAGC	19013
rs36358963	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85771007	CCATGATTCCCACTC[C/T]GCCTTGGTACTAGGA	19013
rs36380917	snp	A/C	0.132653	0.220748	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85772239	GCCTTTGTAGACTAG[A/C]ATTAGTGAGTCCGGA	19013
rs36384844	snp	C/T	0.21875	0.248039	intron-variant	Ppara	Mm_Celera	15:85758976	TGCATACCTGAAATC[C/T]ATCTCACGTGGCTGT	19013
rs36385560	snp	C/T	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85785847	TTATTTTTGTTCAGA[C/T]CTGTTCCTGAATCAG	19013
rs36397157	snp	A/G	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85748455	GAACCCTCTGCCATG[A/G]GAGAGAACAAGATGA	19013
rs36399557	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770994	TAGTGAGTGAGACCC[A/G]TGATTCCCACTCCGC	19013
rs36404607	snp	A/G	0.142012	0.225474	utr-variant-3-prime	Ppara	Mm_Celera	15:85804329	GTTTAAAGTTTTCCC[A/G]GTGTCCCCTGAGATT	19013
rs36405525	snp	A/G	0.32	0.24	intron-variant	Ppara	GRCm38.p3	15:85755577	GGTAGGAAGTAGACG[A/G]AGCATTATGGCCAGA	19013
rs36408981	snp	G/T	0.408163	0.193609	intron-variant	Ppara	Mm_Celera	15:85756822	TGCAAATGGAGAGAG[G/T]CCCGGAGCCTATTTA	19013
rs36417329	snp	C/T	0.459184	0.136902	utr-variant-3-prime	Ppara	Mm_Celera	15:85805315	GGGAGAAATAACGCT[C/T]TTCTCTCACCTCTTT	19013
rs36428438	snp	A/G	0.486111	0.0821678	intron-variant	Ppara	GRCm38.p3	15:85757031	CAGAAAAGGAAAGCC[A/G]TGGGCAGGTTTCAGA	19013
rs36435780	snp	C/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85768353	GCTCCATTTGCTAAA[C/T]GAGCAGACTAATAGA	19013
rs36460189	snp	A/T	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85763259	TGCTTCAAGGGGAAC[A/T]GGACAGATTCCTCCT	19013
rs36462604	snp	G/T	0.132653	0.220748	intron-variant	Ppara	Mm_Celera	15:85756680	GGACAAAATAATTAC[G/T]CTCCCAAGTTTCTTT	19013
rs36473594	snp	C/G	0.124444	0.216185	utr-variant-3-prime	Ppara	Mm_Celera	15:85803101	CTCTTAGGAATCAGA[C/G]GGCAGAGCAAGTCAT	19013
rs36474893	snp	C/T	0.132653	0.220748	utr-variant-3-prime	Ppara	Mm_Celera	15:85804328	AGTTTAAAGTTTTCC[C/T]GGTGTCCCCTGAGAT	19013
rs36485779	snp	C/T	0.124444	0.216185	intron-variant, utr-variant-3-prime, downstream-variant-500B	Ppara, Cdpf1	Mm_Celera	15:85807329	CAGTTCAAAGAAGAC[C/T]GGGTCCACAGCTCCC	19013
rs36488219	snp	A/T	0.197531	0.244432	intron-variant	Ppara	Mm_Celera	15:85763782	AAGAGAGCCATTTAA[A/T]GTGAAATACACAGGA	19013
rs36493396	snp	A/G	0.489796	0.070696	intron-variant	Ppara	Mm_Celera	15:85767835	AAATATTTTAAAAAC[A/G]TTAAGCAAATACATA	19013
rs36497029	snp	C/T	0.132653	0.220748	intron-variant	Ppara	Mm_Celera	15:85744708	TTATCCTGAGTCAGC[C/T]TGCACTCTCCCCTCT	19013
rs36531169	snp	C/T	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85756506	TAGTGTCCATGCCAC[C/T]TTAAACCATGTTGGT	19013
rs36538069	snp	A/G	0.197531	0.244432	intron-variant	Ppara	Mm_Celera	15:85762820	TAACAAAAAGCCCAG[A/G]CCAAGTGGATTCTGC	19013
rs36542768	snp	A/G	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85762780	AATGGCCGGCCCCTT[A/G]TCATGAGGGATAACA	19013
rs36545450	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Ppara	Mm_Celera	15:85806411	CTGCCACTTGCTCAC[C/T]ACTGTCCTTGGTGCC	19013
rs36550327	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770443	TCTTAAGATGGTGCC[A/G]CTCTTGAAGTCCAGC	19013
rs36559548	snp	A/G	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85791891	TTCTCCAATGAAGTG[A/G]GTTGAGACATTTTAG	19013
rs36564150	snp	C/T	0.132653	0.220748	intron-variant, utr-variant-3-prime, downstream-variant-500B	Ppara, Cdpf1	Mm_Celera	15:85807149	CTAGGTGTCTTCCCA[C/T]GTGTGCATCTACAGG	19013
rs36589429	snp	C/G	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85797051	TTGCTGATTTCTACA[C/G]GAAGCCAGTCCTGAT	19013
rs36592631	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85775034	ACTTCATGGCTGATA[C/T]CACGATTGGCGCTTT	19013
rs36609432	snp	A/G	0.132653	0.220748	intron-variant	Ppara	Mm_Celera	15:85795002	AAGATCAATAGACCC[A/G]CTGCGCTTCTGTCGC	19013
rs36609671	snp	A/G	0.231111	0.249285	intron-variant	Ppara	Mm_Celera	15:85792424	CTGTCAGAGCTCAGG[A/G]GAATCAGGACTCACA	19013
rs36616945	snp	A/G	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85763290	CTGTAGTGGGGAGCA[A/G]TGACCTGGCGCAACA	19013
rs36621510	snp	C/T	0.152778	0.230321	intron-variant	Ppara	Mm_Celera	15:85754856	GGTGACTGAGGTGGA[C/T]CTGGTAACGTAAAAT	19013
rs36651261	snp	A/C	0.260355	0.249785	intron-variant	Ppara	Mm_Celera	15:85755469	GCTCTGCCAGCACAC[A/C]CGGGTAGTTGAGAGC	19013
rs36655534	snp	C/T	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85742986	GCAGGAGCCTAAAGT[C/T]CTTGAAATTTCAGAT	19013
rs36663300	snp	A/G	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85763039	CAGATGGTAGGAGGA[A/G]AAAGATCTCTGGCCC	19013
rs36677578	snp	A/T	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85758932	TCTTTAGCTATTGTT[A/T]TGGCGGTATGCATTT	19013
rs36682881	snp	A/G	0.124444	0.216185	utr-variant-3-prime	Ppara	Mm_Celera	15:85801465	ATGGGGGTGATCGGA[A/G]GCTAATAGGATTCAG	19013
rs36688001	snp	A/C	0.132653	0.220748	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85776346	CTGAGTCAGGGCCTA[A/C]TGAAGGCAGCTGTGA	19013
rs36693878	snp	A/C	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85791683	CCTCCTTGGCACATG[A/C]GGACTCTTGCCTGTA	19013
rs36708338	snp	A/C	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85795106	TCCCAAATTATCCCC[A/C]AAAAGTGGTTATCGG	19013
rs36711712	snp	A/T	0.345679	0.230967	intron-variant	Ppara	Mm_Celera	15:85761207	TCTTGAGCTAAAACC[A/T]CCAAAGGACCCATTT	19013
rs36715933	snp	A/G	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85747817	CTTCCTTTCACTTCA[A/G]AAAGCATCTATCCTC	19013
rs36735672	snp	A/T	0.408163	0.193609	intron-variant	Ppara	GRCm38.p3	15:85773731	CCCAGATGTTGTCTT[A/T]GGATGCTGGGTGCTG	19013
rs36763858	snp	A/G	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85757569	TGGCTAAAATGGTAG[A/G]TAGTTACACTGGGGA	19013
rs36795141	snp	A/C	0.489796	0.070696	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Ppara	GRCm38.p3	15:85771488	ATCGAAGCTTCCAAA[A/C]GACAAATCCAAATGC	19013
rs36802193	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85770706	CTATTTGTTACAGTT[A/G]TAGCTGATACAACTC	19013
rs36817188	snp	A/G	0.244898	0.249948	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85776736	GTCATTTATTTTCTA[A/G]AACCATCTACTATAC	19013
rs36825479	snp	C/T	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85785884	AAGTAAGCAGAGATG[C/T]GATTTTTCTCATGAC	19013
rs36831994	snp	A/G	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85789236	CTATCTCCAGCAGCT[A/G]GTATATTTAGCAGAG	19013
rs36852158	snp	C/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85760309	AGAAAACACACTCCT[C/T]GTGATGTTGATTATT	19013
rs36857746	snp	A/G	0.493827	0.0552116	intron-variant	Ppara	GRCm38.p3	15:85762734	AATCCAAGTGGCCTT[A/G]TTGAAGCCAACTTAT	19013
rs36863683	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85769479	ACCAAAGAGAGGTAC[A/G]TCCGAATGTTGCCGA	19013
rs36866264	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85775279	GCACAGGTTTCTTGC[A/G]TACCATAACATAAAC	19013
rs36870211	snp	C/T	0.48	0.0979796	intron-variant	Ppara	GRCm38.p3	15:85795233	TGTTCTGACTTGAAA[C/T]GTTCAGCTTGGCTCA	19013
rs36878020	snp	C/T	0.197531	0.244432	intron-variant	Ppara	Mm_Celera	15:85759448	AGCAGTATTTTGTGG[C/T]TTCTGCTTCAAGTTT	19013
rs36912457	snp	A/G	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85799161	CCGTAGTCCTGCACC[A/G]ACCCCGTGGGTATGG	19013
rs36914929	snp	A/C	0.486111	0.0821678	intron-variant	Ppara	GRCm38.p3	15:85756985	GGTGAGAGCTACCAA[A/C]GGTATCCCTTGAAAG	19013
rs36925423	snp	A/G	0.5	0	intron-variant	Ppara	Mm_Celera	15:85795725	AGCATGGGGTGGGGC[A/G]TGTCACATACCTCCT	19013
rs36929256	snp	C/T	0.336735	0.234472	intron-variant	Ppara	Mm_Celera	15:85773390	TCCTCTGTCTCTTCA[C/T]GTTTGCTGTCTGCTG	19013
rs36942433	snp	C/T	0.197531	0.244432	intron-variant	Ppara	Mm_Celera	15:85758767	TCATAACTGAGCATC[C/T]TTGTCCTTGCTGCTG	19013
rs36962862	snp	A/G	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85767295	ATATATGTGTAGTGG[A/G]TGATTTGTGAAAAAC	19013
rs36970049	snp	A/G	0.124444	0.216185	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85776766	CCCTGGCCTTCATGT[A/G]TATAGGAAGAGCACT	19013
rs36981016	snp	C/T	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85758385	TGTATTTACTGCTAT[C/T]TTTTGGCAGGGTTAC	19013
rs36981144	snp	A/G	0.165289	0.235211	intron-variant	Ppara	Mm_Celera	15:85752030	CCTTTCACCAAGTAG[A/G]AAGAGTCCCTGAGTC	19013
rs36985795	snp	A/G	0.497041	0.0383476	intron-variant	Ppara	GRCm38.p3	15:85756495	TTCCGTTCCCTTAGT[A/G]TCCATGCCACTTTAA	19013
rs36988046	snp	A/G	0.132653	0.220748	intron-variant	Ppara	Mm_Celera	15:85743703	ATTTTAGATGCATGA[A/G]GGCGTTAAGTCAAAC	19013
rs36994391	snp	A/G	0.231111	0.249285	intron-variant	Ppara	Mm_Celera	15:85792367	TGCTGAGTCGCCTCC[A/G]TTTTCTTCACCACAA	19013
rs37000190	snp	A/C/G	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85758906	TTTGTCATGTTCTGC[A/C/G]CAGTGTCTTTTCTTT	19013
rs37030235	snp	A/G	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85791638	GGGTACAAGAAGGGG[A/G]TCAAGAGCCATTTTC	19013
rs37059314	snp	C/T	0.132653	0.220748	intron-variant	Ppara	Mm_Celera	15:85739802	CTCAGGCTTCCTGCA[C/T]GCATGTGGCTCTCCA	19013
rs37062186	snp	C/T	0.486111	0.0821678	intron-variant	Ppara	GRCm38.p3	15:85756947	AAGAGGTACTGAAGA[C/T]GTTTCTATGTTCTGT	19013
rs37065511	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Ppara	Mm_Celera	15:85771874	GGTCACGCCTTCAGC[A/G]TTGTTGAGCAAGAAC	19013
rs37079075	snp	A/G	0.48	0.0979796	intron-variant	Ppara	Mm_Celera	15:85759543	AAATCTTTCCTCTCC[A/G]AGTTGTTTTGGCCAT	19013
rs37085640	snp	A/T	0.132653	0.220748	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85775752	TACAGTTTCTCCCTG[A/T]GGGTCATGAGCACCC	19013
rs37096204	snp	A/G	0.152778	0.230321	intron-variant	Ppara	Mm_Celera	15:85796169	TTTAAACTCCTCATG[A/G]AACTCGTAAGGTATC	19013
rs37102851	snp	C/T	0.197531	0.244432	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85769843	CCTTCTCTGAGGAAT[C/T]TTCTTGAATTCACGG	19013
rs37105939	snp	A/G	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85763136	AGAACCAATCAGAGA[A/G]GTTTAGAGGGAAACA	19013
rs37106663	snp	A/G	0.124444	0.216185	utr-variant-3-prime	Ppara	Mm_Celera	15:85803838	CCAGCACTGATGGCA[A/G]AGTCTTAGTGCCAGA	19013
rs37148838	snp	A/G	0.444444	0.157135	utr-variant-3-prime	Ppara	Mm_Celera	15:85804862	CTCCTGGCTCATCAG[A/G]AAAAGATGTATGGTC	19013
rs37168110	snp	A/G	0.459184	0.136902	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770516	GGACCAATCAGGAGC[A/G]TCAGTTGATGGGCAT	19013
rs37177370	snp	C/T	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85773502	CCTGGCATCCCTTGT[C/T]TCCACAGCTCTCAAT	19013
rs37181324	snp	A/G	0.345679	0.230967	intron-variant	Ppara	Mm_Celera	15:85748623	CTCAACTGTGGACCT[A/G]GCAGGGGGAGCTAGC	19013
rs37192519	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Ppara	Mm_Celera	15:85771570	CTGATTGCAACAGGC[A/G]CAGAATGTGTCCAAG	19013
rs37196333	snp	A/G	0.408163	0.193609	intron-variant	Ppara	Mm_Celera	15:85772667	TGGCGATGGGTCCAA[A/G]TTAACCCACAGTAAC	19013
rs37207536	snp	C/T	0.486111	0.0821678	intron-variant	Ppara	GRCm38.p3	15:85787462	CTGAGAGGCGCATAT[C/T]CTTTAAACCAAAATG	19013
rs37210028	snp	G/T	0.473373	0.11227	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85769878	TTTCCCTCTGCTCTG[G/T]TCCCAGAATCCTCCT	19013
rs37224470	snp	A/T	0.18	0.24	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85776035	AAAGGCATGCACCAC[A/T]CATTTCTTGAGGAAG	19013
rs37237897	snp	A/G	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85763434	CAAGGCTCTTCCACA[A/G]CAAGCAAGAAGAGAT	19013
rs37245191	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85769627	TCAGCGATTTGATGG[C/T]GTTAACTCCTTTTCT	19013
rs37261110	snp	A/G	0.124444	0.216185	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85772244	TGTAGACTAGAATTA[A/G]TGAGTCCGGAGCCGC	19013
rs37264522	snp	A/G	0.124444	0.216185	utr-variant-3-prime, intron-variant, downstream-variant-500B	Ppara, Cdpf1	Mm_Celera	15:85806738	TATCCTGAATTTATG[A/G]GAACCCGTATGTTTG	19013
rs37270036	snp	C/T	0.459184	0.136902	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770470	CAGCAGCTTCCAGTC[C/T]TAGTAAGAGGATGGG	19013
rs37279042	snp	A/G	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85761582	AAGAATCACCAGGAT[A/G]GCCTAGCATGTTCTT	19013
rs37281678	snp	G/T	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85796863	CCTGCTCAGTAGACT[G/T]TATAAAGTGGCAGAC	19013
rs37282986	snp	A/G	0.336735	0.234472	intron-variant	Ppara	GRCm38.p3	15:85793260	TGTGCATGCCTCTGT[A/G]TGCGTGAATATGTGT	19013
rs37283295	snp	C/T	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85795278	GAATGTTGTCACTTG[C/T]CCATGAGTCACTCTA	19013
rs37302914	snp	A/T	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85750224	ACCAGTGGTGATGTC[A/T]GAGGGGACTTTGGAA	19013
rs37303815	snp	G/T	0.244898	0.249948	intron-variant	Ppara	GRCm38.p3	15:85766789	CAAACCCCTGTTTCT[G/T]GGCAACGGTAGAGAA	19013
rs37307017	snp	A/C	0.277778	0.248452	intron-variant	Ppara	Mm_Celera	15:85743033	TCTCCTCCAAAAATT[A/C]TGCTTTGTCCAAGGT	19013
rs37309388	snp	A/T	0.260355	0.249785	intron-variant	Ppara	Mm_Celera	15:85753831	AAGTCATTCTTTCAA[A/T]TATGCTCTTTTAAAG	19013
rs37366824	snp	A/C	0.132653	0.220748	intron-variant	Ppara	Mm_Celera	15:85744162	GGTGAATATTTAACT[A/C]TGCTCAAGGGCAGCT	19013
rs37393549	snp	C/T	0.297521	0.245442	intron-variant	Ppara	Mm_Celera	15:85742968	GTGCCTGCTGCTTCC[C/T]GAGCAGGAGCCTAAA	19013
rs37416979	snp	C/T	0.18	0.24	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85769565	CCCACTCTCACCCTG[C/T]GGATGGCTTTCTGAA	19013
rs37420502	snp	A/G	0.124444	0.216185	utr-variant-3-prime	Ppara	Mm_Celera	15:85802061	AGACCCTCAGCGTGT[A/G]GGCATGGCAGCAATA	19013
rs37422556	snp	C/T	0.260355	0.249785	intron-variant, utr-variant-5-prime	Ppara	GRCm38.p3	15:85776034	TAAAGGCATGCACCA[C/T]TCATTTCTTGAGGAA	19013
rs37429188	snp	A/G	0.497778	0.0332592	utr-variant-3-prime	Ppara	GRCm38.p3	15:85801997	TAGTGTCCGATAGAC[A/G]AAGACAGGATGAGCC	19013
rs37445377	snp	A/C	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85792278	TGTCTCCCTCAGACT[A/C]TGAGACTTAGAACAG	19013
rs37455177	snp	C/G	0.124444	0.216185	utr-variant-3-prime	Ppara	Mm_Celera	15:85801553	TGCACAGCACTCTAC[C/G]TTGCGTTTATAATTC	19013
rs37460453	snp	C/T	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85748224	GATGAAGATGTCGGT[C/T]GCTTTGCCTTAGGCC	19013
rs37475393	snp	A/G	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85763505	AGACTCAGGAAGAGA[A/G]GCCTCATAATGAGGA	19013
rs37496507	snp	A/G	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85759313	CCTGTGTCTGTGTCT[A/G]AGGGGAACTGTCTTG	19013
rs37519533	snp	A/C	0.21875	0.248039	intron-variant	Ppara	Mm_Celera	15:85758564	TTCCATTTTTGAAAA[A/C]AACATGGCCTCATTT	19013
rs37520429	snp	A/G	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85756747	CTCTGGGGACCGCTC[A/G]TTCCAAACAGGAAAG	19013
rs37526259	snp	C/T	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85767555	CAATCACACCAAAGA[C/T]CAAACCAGGCCTTGC	19013
rs37573381	snp	A/T	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85793025	GCCTTCATCTCTTCC[A/T]GCCCAGACTGCTGGC	19013
rs37591805	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Ppara	Mm_Celera	15:85771918	AATGATTGGAGCTGT[A/G]TTGGACTTGACTTGT	19013
rs37598894	snp	A/G	0.124444	0.216185	intron-variant, utr-variant-3-prime, downstream-variant-500B	Ppara, Cdpf1	Mm_Celera	15:85807150	TAGGTGTCTTCCCAC[A/G]TGTGCATCTACAGGG	19013
rs37615513	snp	A/T	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85795682	CTGTATATCTCTCTG[A/T]GGTTGCTGAAGATGC	19013
rs37644353	snp	C/T	0.21875	0.248039	intron-variant	Ppara	Mm_Celera	15:85762336	CATCAGAAGAGAATA[C/T]GGATTTTAGAAAACA	19013
rs37648949	snp	A/G	0.132653	0.220748	intron-variant	Ppara	Mm_Celera	15:85794669	CTCTGCTAGAGAAGC[A/G]TTCCCAGCACATACC	19013
rs37650462	snp	C/T	0.48	0.0979796	intron-variant	Ppara	GRCm38.p3	15:85756648	TGCTGTGGCCCTTCA[C/T]TCTCTTACTTGGAGG	19013
rs37697719	snp	C/T	0.197531	0.244432	intron-variant	Ppara	Mm_Celera	15:85760180	CCAAATCTGTTTTTG[C/T]GACTTCCACTTGACT	19013
rs37723208	snp	C/T	0.197531	0.244432	intron-variant	Ppara	GRCm38.p3	15:85767318	TGAAAAACCTGTCAG[C/T]GTGGCTACCTAGTGA	19013
rs37730136	snp	C/T	0.132653	0.220748	intron-variant	Ppara	Mm_Celera	15:85790755	AGTGTGACCTACCAC[C/T]CTTTCTTTTGCCTCT	19013
rs37755750	snp	A/T	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85743015	ATTGTGGCCTCCATT[A/T]TCTCTCCTCCAAAAA	19013
rs37758322	snp	A/G	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85747774	CAGCCCTTCTGCTCC[A/G]TAGAGTACCAGGGCG	19013
rs37813356	snp	A/G	0.124444	0.216185	utr-variant-3-prime	Ppara	Mm_Celera	15:85804932	CCTGTCACCAGCCTG[A/G]GACCCCTGAGGACAT	19013
rs37826576	snp	A/C	0.336735	0.234472	intron-variant	Ppara	Mm_Celera	15:85797065	ACGAAGCCAGTCCTG[A/C]TCATCATATATTTAT	19013
rs37831460	snp	A/G	0.21875	0.248039	intron-variant	Ppara	Mm_Celera	15:85755666	GCCAGAGGAAGACAG[A/G]ACAGCCTTTCAAAAT	19013
rs37859952	snp	A/G	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85763370	CCAGAATTTGTCCAA[A/G]TAATTTAGCTGCATC	19013
rs37864101	snp	C/T	0.444444	0.157135	intron-variant	Ppara	GRCm38.p3	15:85762469	TGCGAGCATGCCTGG[C/T]ACCCCAGACAGGATG	19013
rs37867459	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85770320	TGAGTGCAGATCTCA[C/T]CCTGCTGCTGGGGCA	19013
rs37870615	snp	A/G	0.231111	0.249285	intron-variant	Ppara	GRCm38.p3	15:85758164	GGTTCATAAGATGTC[A/G]TTCCACCACCATGGT	19013
rs37882604	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85775427	TTACACGTGTGCCCC[A/G]TACACATGCTTGTCT	19013
rs37890435	snp	C/T	0.495868	0.0452663	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85769856	ATTTTCTTGAATTCA[C/T]GGAGGGTTTCCCTCT	19013
rs37896494	snp	C/G	0.152778	0.230321	intron-variant	Ppara	Mm_Celera	15:85748312	ACCATCCATCTCTAA[C/G]GTATAATGAGTTGAT	19013
rs37908159	snp	A/C	0.231111	0.249285	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Ppara	Mm_Celera	15:85771361	ATTTTTTGTGCCAGC[A/C]GCCTTTTGTGCCAGT	19013
rs37939224	snp	C/T	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85741082	TTTAGGTATTGCCTG[C/T]CCCTATGGAGACTGC	19013
rs37945684	snp	A/C	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85761674	ACAATACTCATTAAT[A/C]CCAATGTATCTGCAT	19013
rs37956635	snp	C/G	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85742821	GACCATGGGAATCAG[C/G]CTGGCAGTGTGTGAC	19013
rs37968628	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Ppara	Mm_Celera	15:85805220	AGGCAAGGAGAAGCA[C/T]CGTTTTGTGTCATAG	19013
rs37977606	snp	A/G	0.408163	0.193609	intron-variant	Ppara	Mm_Celera	15:85759400	AGGTTGACTATACAA[A/G]AAAGCTACCTTAGCA	19013
rs37979731	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Ppara	Mm_Celera	15:85771498	CCAAACGACAAATCC[A/G]AATGCCTCGTTAGTT	19013
rs38035614	snp	A/G	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85794694	CATACCAGGTCCCGA[A/G]TTCAGTCTCCAGTAT	19013
rs38042658	snp	A/G	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85743810	TTGCCACTGGACCTG[A/G]AACCCAAATGGGACC	19013
rs38074116	snp	A/G	0.244898	0.249948	utr-variant-3-prime	Ppara	Mm_Celera	15:85802290	AGAAGGGAGCTGGTC[A/G]CCTTGGAGAACAAGA	19013
rs38095450	snp	C/T	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85746908	TGCCTCGGATGAGTC[C/T]AGCAGCCTCAGAGCA	19013
rs38097019	snp	A/G	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85768639	CACCTATACTACTTG[A/G]TGGAACATGCACTAT	19013
rs38110376	snp	C/T	0.132653	0.220748	intron-variant	Ppara	Mm_Celera	15:85773768	TGACTGGGTGATACC[C/T]GAGTAGTAGCTGCTC	19013
rs38152207	snp	A/G	0.244898	0.249948	intron-variant	Ppara	Mm_Celera	15:85743528	TGATCAACGCAGGAC[A/G]AAGCCACGTATGGTG	19013
rs38164530	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85775263	CCAAGTAATAAAGTA[A/G]GCACAGGTTTCTTGC	19013
rs38166406	snp	A/G	0.408163	0.193609	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Ppara	GRCm38.p3	15:85771542	TGTGACAGACTCCTG[A/G]ACTCAGCCAGCTCTG	19013
rs38180101	snp	A/C	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85758952	GGTATGCATTTCTCA[A/C]TGTTAAATTGCATAC	19013
rs38206585	snp	C/T	0.48	0.0979796	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85770243	CTTTTAGGTAGCCTC[C/T]GGGTGTAGAGGGACA	19013
rs38208931	snp	A/C	0.32	0.24	intron-variant	Ppara	Mm_Celera	15:85755798	GCATGGCTGTCCCTA[A/C]CCTCAGGTATGCCTG	19013
rs38251360	snp	C/T	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85763578	ATTGGATTTAGCAGC[C/T]GGGTACATTAAAGTC	19013
rs38275915	snp	A/G	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85756874	ACACAAGATACCTTG[A/G]GCTAGAAATTCTCAA	19013
rs38288397	snp	A/G	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85762303	AAACAGCGCTAGAGA[A/G]TATGAGATGTTTCTG	19013
rs38300999	snp	A/G	0.486111	0.0821678	intron-variant	Ppara	GRCm38.p3	15:85748429	cacacacacacacCA[A/G]GCTCACTGCAGAACC	19013
rs38306580	snp	A/G	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85743470	GTCTAAACCTGCGCC[A/G]AGCCAATGCTCTTCG	19013
rs38311399	snp	A/G	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85755870	CGTCATGACTTCACC[A/G]AGTGCTCAACTTGTT	19013
rs38322952	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85774701	CGTCCAGAGTTCACG[C/T]TGAGATTGCTCTCCT	19013
rs38369913	snp	A/C	0.124444	0.216185	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85770771	TTCCCAGTAACATCT[A/C]GGGTCATTCATGTAT	19013
rs38386845	snp	C/G	0.132653	0.220748	utr-variant-3-prime	Ppara	Mm_Celera	15:85803724	TGAGAAAGCTGGCAG[C/G]TATGCTCTGCAAGGT	19013
rs38412359	snp	C/T	0.132653	0.220748	intron-variant	Ppara	Mm_Celera	15:85790597	AAAGAAATGATAACT[C/T]ACTTTCATTCCCTTC	19013
rs38419961	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Ppara	Mm_Celera	15:85804184	GCATCTGATCCTAAA[C/T]ATGTCTCACCTTGAG	19013
rs38427490	snp	A/G	0.497041	0.0383476	intron-variant	Ppara	GRCm38.p3	15:85772612	GATATCTAGGAAGTG[A/G]CTTGTCGATCCAAGA	19013
rs38428581	snp	C/T	0.336735	0.234472	intron-variant	Ppara	Mm_Celera	15:85743690	TGAAGCAGAAAGGAT[C/T]TTAGATGCATGAGGG	19013
rs38433869	snp	A/G	0.336735	0.234472	intron-variant	Ppara	Mm_Celera	15:85796893	CCTGCAGGTGTGGAT[A/G]CCATGGTACTGCATC	19013
rs38440354	snp	G/T	0.375	0.216506	intron-variant	Ppara	Mm_Celera	15:85761434	GAAGATGCTGGACTT[G/T]TCCTATTCTTTCAGC	19013
rs38452541	snp	C/T	0.48	0.0979796	intron-variant	Ppara	Mm_Celera	15:85763366	AGGACCAGAATTTGT[C/T]CAAGTAATTTAGCTG	19013
rs38457619	snp	A/C/T	0.408163	0.193609	intron-variant	Ppara	GRCm38.p3	15:85793209	TCAAGAGACCATAGA[A/C/T]CTTTGATAAGATTTA	19013
rs38466823	snp	C/T	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85741063	CAGCTTACTGGAGCT[C/T]ATGTTTAGGTATTGC	19013
rs38496028	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85774915	GGAATAAAGGCTGCT[A/G]TCGGAGGCAGTGACA	19013
rs38617985	snp	A/G	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85800308	TTGAGACTGTACCAG[A/G]AAGGCTACCTAGTGT	19013
rs38653448	snp	C/T	0.132653	0.220748	utr-variant-3-prime	Ppara	Mm_Celera	15:85806149	GTCAGGGCCACTGTG[C/T]AGGCCTCTTAGGCTA	19013
rs38697109	snp	C/T	0.408163	0.193609	intron-variant	Ppara	GRCm38.p3	15:85768320	TCAAGTGGCTGCAGG[C/T]AGGGACAACCTACAA	19013
rs38789321	snp	A/G	0.489796	0.070696	intron-variant	Ppara	GRCm38.p3	15:85796927	AAGGGAGCCCGGCTG[A/G]GATCTGGGATCTGGC	19013
rs38883890	snp	C/T	0.489796	0.070696	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770135	TGCCAGTTACTAAGC[C/T]AGGGTCCTTGTCTGT	19013
rs38907888	snp	C/T	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85758315	ACTTGTCTGCTGCAA[C/T]GTATACCCATTCCTT	19013
rs38995463	snp	G/T	0.132653	0.220748	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85774237	CATGTCTGTTTCTTT[G/T]GCTTCCTATTTACTG	19013
rs39100941	snp	A/G	0.142012	0.225474	intron-variant	Ppara	Mm_Celera	15:85742840	GCAGTGTGTGACAGC[A/G]GTGCCCTTGGACTTC	19013
rs39141887	snp	A/G	0.5	0	intron-variant	Ppara	GRCm38.p3	15:85795518	GCCCCACAATGAGCC[A/G]TCTTTACTACACCAT	19013
rs39226829	snp	C/T	0.197531	0.244432	intron-variant	Ppara	Mm_Celera	15:85759583	TCATAGCAACAGAAA[C/T]GAGACAGGAGTACTT	19013
rs39248004	snp	A/T	0.375	0.216506	intron-variant	Ppara	GRCm38.p3	15:85762381	GACCTGGCTTAGCAG[A/T]TATAAGCACACTTGC	19013
rs39362271	snp	C/G	0.124444	0.216185	intron-variant	Ppara	Mm_Celera	15:85789261	GCAGAGCACTTGAAA[C/G]TCTTATGGTGAGACA	19013
rs39504571	snp	A/G	0.124444	0.216185	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85776047	CACTCATTTCTTGAG[A/G]AAGCCAAACCATCTC	19013
rs39949675	snp	A/G	0.231111	0.249285	synonymous-codon, intron-variant	Ppara	Mm_Celera	15:85801102	GCAGAGCAACCATCC[A/G]GATGACACCTTCCTC	19013
rs45720835	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85766255	CTAGGAACACATCTA[C/T]ACCAGTAAACAGCAC	19013
rs45808142	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85762017	TAGCTCTGGGTGATA[C/T]ATCAGCCTTTTCTGG	19013
rs45809630	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85793814	TTAAAAACAGTGCTT[C/G]CTCTTAACTGCTGAG	19013
rs45816277	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85729277	ATCCTTCCTGAGGCT[C/T]GCAAACAGAGGGAAA	19013
rs45832353	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85796038	CTATATACATTTGTG[A/G]GGTAGAGTTTGGAAA	19013
rs45839187	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85751050	GTGCACATGGTGCTT[A/G]TATGGTGGTACAAGC	19013
rs45849893	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85752300	ACAGTGGTGGTCTGG[A/T]CTGGAGAGAGGGAGG	19013
rs45868981	snp	C/T			upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85732903	TTCCTGGAAAGGTCT[C/T]ACATAAGTTGCAAGG	19013
rs45892654	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85730578	GTTCGAGGCCAGCCT[G/T]GTCTACAGAGTGAGT	19013
rs45934659	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85728719	ACCCAGGAATGAATA[A/G]GCTGAGTTTTCCCCA	19013
rs45934751	snp	A/G			upstream-variant-2KB	Ppara	GRCm38.p3	15:85728174	TTCAACCCCTGCCCC[A/G]CCCCCCCAGCAACCC	19013
rs45943609	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85732196	CAGTGAGTTTATAGC[G/T]TCTCTGCCCAGGTGA	19013
rs45972139	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85743558	GGCCTACGCCTATAA[C/T]CCGCACTGGGGAATC	19013
rs46000769	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85755708	GAAAGCAGACGGTTC[A/G]AAGGGGACCAGCTCT	19013
rs46017610	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85749015	CACCTTGAGATCATG[C/T]ACAGACAGCAAACAT	19013
rs46020631	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85748523	TCATCCCATGGCCCC[C/T]CGTGGCTTCTGCCTG	19013
rs46021292	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85780868	AATTAGATCTGGTGA[A/G]TTCTTTACAGATTCT	19013
rs46022419	snp	G/T			intron-variant	Ppara	GRCm38.p3	15:85757876	TGTATTTATGTTTGG[G/T]GTGTGTGTGTGTGTG	19013
rs46023646	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85797103	ATTTATTCAAAAGTC[A/G]GTGCTAAATAATGAT	19013
rs46027134	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85779612	CTGGGTCTCTGGAAT[C/G]GGGGGACAGTTGTAG	19013
rs46028204	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85768401	CATTCAGCAGCATGA[A/G]CCTCTCCCCAACAGT	19013
rs46037809	snp	C/T			utr-variant-3-prime	Ppara	Mm_Celera	15:85803652	ACCTAGTCAGATTTC[C/T]CAAGGCCTTAGTAAC	19013
rs46071621	snp	A/C			intron-variant	Ppara	GRCm38.p3	15:85766535	GGTGAACAAGGAATC[A/C]AAAATTCTACTAAAA	19013
rs46073082	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85766319	CCTTTCAAAAACCCA[C/T]TTCCAGAAGAAATAT	19013
rs46088750	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85729103	CCGTTCTCCAGCCAG[C/G]TAACCACTTTTTACT	19013
rs46174098	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85759493	GTCTAGACTTCCCTC[A/G]GCAATGAACTATGAC	19013
rs46179292	snp	C/T			upstream-variant-2KB	Ppara	Mm_Celera	15:85727179	CGCACCAGAAGAGGG[C/T]GTCAGATCTTGTTAT	19013
rs46192923	snp	C/G			utr-variant-5-prime	Ppara	Mm_Celera	15:85728361	CCTTCTCCTGGGCCT[C/G]GGACAGGTTAGGACA	19013
rs46198471	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85731329	AAACAGACAAAGCAC[A/T]TTTCGTTTGTTTGTT	19013
rs46208528	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85755668	CAGAGGAAGACAGAA[C/T]AGCCTTTCAAAATAA	19013
rs46237685	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85729203	TCCAGGGACATGGAA[C/T]GCTTCTCACACCATG	19013
rs46276153	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85728586	CATGTGGCCGGCACC[A/C]TCCATCAGCAAGAAA	19013
rs46287506	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85750001	AGCACATACTTGACA[C/T]GGATGGGAGGAAGGA	19013
rs46320887	snp	C/T			upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85732993	GCAGGTAGTAGGGTT[C/T]CCATGCTTTCTGCAT	19013
rs46323875	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85728978	AGCACCGCCACGTAG[A/G]TTTAGAGTAGTTTTA	19013
rs46344360	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85728612	AGAAAAACCGAAAGT[C/T]GGTCTTCTGTGGGAG	19013
rs46370986	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85749879	TGGAGTATACATGGG[A/G]AAGGATGGGGTTGAA	19013
rs46406570	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85784310	GCATGCCCAGGCTTT[A/G]CTCAGAGATGCAATT	19013
rs46416650	snp	C/T			upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733111	CAAGGGCTTTATAGA[C/T]TGGCTTTCTCTCATC	19013
rs46437355	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85757556	GCCCATAGAGACATG[A/G]CTAAAATGGTAGGTA	19013
rs46459568	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85751937	CTGGAGAAGCGCAAA[G/T]TGCCTGTGTTTAAAT	19013
rs46516797	snp	A/C/G			upstream-variant-2KB	Ppara	GRCm38.p3	15:85727453	ACCTTGACCCTTGAC[A/C/G]CTTGGAGCCCACGTG	19013
rs46533104	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85751086	AAACACCATACACAT[A/C]AACACAAATTTAAAA	19013
rs46540747	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85780921	GGAGAGATGGCTCAG[C/T]GGTTAAGAGCACTGC	19013
rs46614249	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85731806	CAGCACCTTTGGGAA[C/T]TGAATCTGTCTTCTT	19013
rs46616644	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85766419	ACAGGTTGCATACAG[A/T]CCTAGAAAATCAAAG	19013
rs46646707	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85795817	GACCACCTCATTAGC[A/G]ATCTGTGCTCACCCA	19013
rs46673380	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85730516	GGCAGTGGTGGCGCA[C/T]GCCTTTAATCCCAGC	19013
rs46674634	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85780254	AGCAGCAAATGCTCT[C/T]GCTCACTGAGCCATC	19013
rs46684755	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85749940	GGGAGGGCTAGAAAG[A/G]CACAAAATATCCCAT	19013
rs46696290	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85729161	GGGGAAAGGCTGGCC[C/T]CATGTCCCTCACTGC	19013
rs46697652	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85729320	ATCTGAGCACTGGGA[G/T]GGTGCCCAGTGTCTT	19013
rs46737063	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85782392	ATATACTGTGTGTGT[A/G]TGTATAGTTGTAAAA	19013
rs46758821	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85766510	AGTAAAACAAAAGAT[C/T]GATGTCCCTGGTGAA	19013
rs46765847	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85729346	GTCTTGTGCCACAGC[C/T]CCATGTGTGTGCAAA	19013
rs46796888	snp	A/G			intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85769985	TGAGACAGTCTCTCA[A/G]TGAACCTGTCATTCC	19013
rs46802484	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85763795	AAAGTGAAATACACA[A/G]GAAAAAGACTTTTTT	19013
rs46806986	snp	G/T			intron-variant	Ppara	GRCm38.p3	15:85763171	CCAGCACTCCCAATG[G/T]GCCAGGCGTCTGGCC	19013
rs46807048	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85768354	CTCCATTTGCTAAAT[A/G]AGCAGACTAATAGAA	19013
rs46872855	snp	C/T			utr-variant-3-prime	Ppara	Mm_Celera	15:85804496	ATAGAGAGTAGGTCC[C/T]GTTCTCCTTCTACAG	19013
rs46888299	snp	A/C			intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770350	AGTCCACATGTGACT[A/C]TCAGTATCTAGAGTT	19013
rs46912956	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85761323	GTGGAGTGTTCTGCT[C/T]GTTTTGATTAGAACC	19013
rs46917323	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85778824	CACTCCAGAAGAGGG[C/T]GTCAGATCTTGTTAC	19013
rs46921555	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85800342	CAGTGGTACTTCCTG[C/T]TATGTCTTCTCTGGA	19013
rs46925231	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85762252	GACTATACTAGGATC[A/T]TTAAGGATCATGGTC	19013
rs46957373	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85799943	GAGGATGCAATGCCC[C/T]CTTCTGGCTTTCTGG	19013
rs46958423	snp	A/C			intron-variant	Ppara	GRCm38.p3	15:85780971	GAGTTCAGTTCCCAG[A/C]AACCACATGGTGGCT	19013
rs46961873	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85757102	GAGAGATGGCTCAGC[A/G]GTTAAGAGCACTGAC	19013
rs46974543	snp	C/T			utr-variant-3-prime	Ppara	Mm_Celera	15:85804507	GTCCTGTTCTCCTTC[C/T]ACAGCCCCGGGGGGC	19013
rs47011395	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85731319	AGGTTCTTGCAAACA[C/G]ACAAAGCACTTTTCG	19013
rs47015435	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85764833	AACAGTGGTGCTTAG[A/G]GAGAAATGTGTAGCA	19013
rs47041634	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85757348	TGAATCATCGATTAA[A/G]GATTTGTGTCTCCTT	19013
rs47061223	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85754575	GTATTTGAGTACTCT[C/T]AAATGGGCAAAGGTG	19013
rs47061558	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85749677	CGAGGTTAGCCTGGT[C/T]TACATAGCAAGTTCC	19013
rs47094051	snp	A/C			intron-variant	Ppara	GRCm38.p3	15:85766405	CGGGAAGAGATAATA[A/C]AGGTTGCATACAGTC	19013
rs47106138	snp	A/G			upstream-variant-2KB	Ppara	Mm_Celera	15:85727478	CACGTGTTCCAACTA[A/G]CACAAGTTTCCCTCT	19013
rs47126625	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85756118	AAAGATTTTTTTATT[A/G]TATGTAAGCACACTG	19013
rs47128487	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85784278	TCTGTGGTGTGGTGG[A/G]CTCTGCATTCCACTA	19013
rs47169502	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85797300	CACTGAGCCACCTCC[A/G]CAGCCTCTTTGTTTT	19013
rs47186863	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85729028	ATACTTGACAGAGAC[A/G]CCAGTTCATTCTGGC	19013
rs47207492	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85763189	CAGGCGTCTGGCCCT[C/T]GTGCAGGTCCAGAAA	19013
rs47214501	snp	G/T			intron-variant	Ppara	GRCm38.p3	15:85763109	AACAGAGCTAGAAGA[G/T]AGGCCAGAAAAAGAA	19013
rs47218060	snp	A/G/T			intron-variant	Ppara	GRCm38.p3	15:85751574	CACAGAGAAAAATGC[A/G/T]GATGGACTCCTCAGT	19013
rs47230170	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85800261	AAGCCCCAGTTATGG[A/G]TGGATAGATGGATGG	19013
rs47237277	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85766478	GGAAATAAAAGTAGA[C/T]GAAGGCATCATGAAC	19013
rs47244375	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85756174	AAGGTGTCAGATCTC[A/G]TTACAGGTGGTTATG	19013
rs47249874	snp	C/T			intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770329	ATCTCACCCTGCTGC[C/T]GGGGCAGTCCACATG	19013
rs47266756	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85751121	ATTTTTTTTAAAGTC[C/T]GAGTGGTATGGTGGC	19013
rs47278728	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85757906	GTGTGTGTATACACG[C/T]GTGCACCTCCATGAG	19013
rs47291830	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85782337	TCTTTGCAAATGCTG[A/C]TAATTTGTTTCTGTA	19013
rs47332260	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85768113	GCCCAAAAAACCCAA[A/G]AAACAAAAACCCAAA	19013
rs47349212	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85732103	ACTTAGGTTTGGAGA[C/T]GGGTTAATTATCAAA	19013
rs47367469	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85729245	TTCCTTCTCTAGGTC[C/T]AGCTGCCCCTCTTAG	19013
rs47405774	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85728547	TGAGGCTACAGAGCT[A/G]GGTCTTGCTTCCAGG	19013
rs47407666	snp	G/T			intron-variant	Ppara	GRCm38.p3	15:85795063	GTTGTTGTTGTTGTT[G/T]TTGTTGTTTTTTCTG	19013
rs47407937	snp	A/G			utr-variant-3-prime	Ppara	Mm_Celera	15:85803666	CTCAAGGCCTTAGTA[A/G]CCCAAGACATGCCAG	19013
rs47429063	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85779871	AGCAATAGCCCAGTG[A/T]CACATAGATAAGTTC	19013
rs47516076	snp	A/G			utr-variant-3-prime	Ppara	Mm_Celera	15:85804641	CCTTGGTCCACATTT[A/G]TATGGCTGACTCCCA	19013
rs47539105	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85780640	CCAATTGGTCCCTGA[A/C]AGAAGGGTTCCTCCC	19013
rs47556439	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85750984	CCCACATGGTGGCTC[A/T]CAACCATCTTTAACT	19013
rs47564701	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85758438	CAACAATAATAATGC[A/G]GAATCATAAATTTCC	19013
rs47610858	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85761246	TGTGGCCTTGGGGGT[C/T]AGATTTTCAGCATGT	19013
rs47612638	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85749354	TAAAAGTAGAAGTGC[A/G]GTGTGGGTGTGTGCA	19013
rs47615250	snp	A/G			upstream-variant-2KB	Ppara	Mm_Celera	15:85727426	CTCAGCAGGTAAGGC[A/G]GCTTGCACCTGACCT	19013
rs47678202	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85729332	GGAGGGTGCCCAGTG[C/T]CTTGTGCCACAGCTC	19013
rs47697982	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85729042	CGCCAGTTCATTCTG[C/G]CACTTCCTCCCAGGG	19013
rs47708481	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85797190	AGCACTAAGTCCCCT[A/G]GAGCTGGAGTCACAC	19013
rs47785612	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85759542	TAAATCTTTCCTCTC[C/T]AAGTTGTTTTGGCCA	19013
rs47796097	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85732311	TATCCCTTCCACAGT[C/T]TCCTCCCCTGAGCCT	19013
rs47840039	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85780299	TGAAATGAATTGGTC[A/G]GTTTTTAAAAATAAA	19013
rs47845272	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85748738	CAGGGGTGAGATGTT[C/T]AGGGTTGCTATTATG	19013
rs47922341	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85796564	GGGTTCATTTTAGCT[C/T]GCAGTTTGAGGGTCA	19013
rs47951447	snp	A/C/G			utr-variant-3-prime	Ppara	GRCm38.p3	15:85803659	CAGATTTCTCAAGGC[A/C/G]TTAGTAACCCAAGAC	19013
rs47980326	snp	A/G			intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85769962	ACCCCCCTCTTTGCC[A/G]TAGTTTGTGAGACAG	19013
rs48009229	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85751931	AAAGGACTGGAGAAG[C/T]GCAAATTGCCTGTGT	19013
rs48018387	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85748783	CTGCCCCTTCCCTGC[A/G]TGAGGCTGGTGTGAG	19013
rs48019410	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85743547	CCACGTATGGTGGCC[C/T]ACGCCTATAATCCGC	19013
rs48042645	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85768889	AGAGCTCTTTAAGTG[A/G]TTTCTGGGGATCGAA	19013
rs48067131	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85754616	CAGGTCAAAGAAATG[A/G]GGGTGGAGGGAGCAG	19013
rs48118215	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85773886	CTCCGTGGTAGAGAT[C/T]GTTCTGGAAGTATGC	19013
rs48120357	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85790635	CCAATGGCCTACCTG[A/G]GGACAGTAAGCCATC	19013
rs48158948	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85749278	GCAAGTCGCACAGTG[C/T]TAGTGGAAGGGTAGA	19013
rs48174399	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85796117	TGACCACCTCCTTAA[A/G]CATCTGTCATCTTGC	19013
rs48184895	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85749646	GGAGGCAGAGGCAGG[C/T]AGATCTCTATGAGTT	19013
rs48222381	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85752331	AAGTGCGTTGGTGAG[C/T]GCGCGTGGGATACTT	19013
rs48312705	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85779415	TCTTTCCTGTGGTAG[G/T]CTGTGCCTTTTGTGT	19013
rs48412064	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85749900	TGGGGTTGAAAGACA[A/G]TGGAGATGGGCAAGA	19013
rs48433643	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85751459	TAGATCAATGAATTT[C/T]ACAGAGCTAATGGAA	19013
rs48444002	snp	C/T			upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733107	GCAGCAAGGGCTTTA[C/T]AGATTGGCTTTCTCT	19013
rs48464826	snp	C/T			upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85732959	GACCCATGGGAGAAT[C/T]TCCAAGCGCTGGTGC	19013
rs48477144	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85762251	GGACTATACTAGGAT[A/C]TTTAAGGATCATGGT	19013
rs48545236	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85757907	TGTGTGTATACACGC[A/G]TGCACCTCCATGAGT	19013
rs48564412	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85731978	TCTGTACACTGTGGG[A/G]GGAAGGGAGAGAGGG	19013
rs48568853	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85752482	CTTCGGCTCTTAATA[C/T]GGGGATATTGGCTCC	19013
rs48608817	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85730369	AGCTATGCTGAATGG[A/T]AGCCAGAATAGGGCA	19013
rs48622059	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85757089	GTGTCTAGGGCTGGA[A/G]AGATGGCTCAGCGGT	19013
rs48661686	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85749275	AGAGCAAGTCGCACA[C/G]TGTTAGTGGAAGGGT	19013
rs48665194	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85749194	AGTTTATGTCTCATC[C/T]GGGTCAGTCAGAATG	19013
rs48678744	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85759266	ACAAAGAACCCTGTA[C/T]CTTCTGGATTTGGCC	19013
rs48688982	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85728713	GAAATGACCCAGGAA[C/T]GAATAGGCTGAGTTT	19013
rs48703196	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85732237	TTGACATAGTTCTCA[A/T]CCCAACTGTTGTTCT	19013
rs48772137	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85729468	CAAGTCTCAACATAA[A/G]CCAGTGTGTTGACTT	19013
rs48801058	snp	A/C			intron-variant	Ppara	GRCm38.p3	15:85761312	ATCTACCACAGGTGG[A/C]GTGTTCTGCTCGTTT	19013
rs48836084	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85780672	TACCTGGTCCTCTTC[A/G]TGTCCTTCAAGCAAG	19013
rs48847615	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85750991	GGTGGCTCTCAACCA[G/T]CTTTAACTCCAGTTC	19013
rs48860685	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85730502	GAAGCTTTCTAGAGG[A/G]CAGTGGTGGCGCACG	19013
rs48869567	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85797016	CTCCTTCTTGCTCTA[C/T]AGAGCTGAACAAGGC	19013
rs48890689	snp	C/T			intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85769957	CCCCCACCCCCCTCT[C/T]TGCCGTAGTTTGTGA	19013
rs48900701	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85731446	GAGATCCAACTTCCT[C/T]TTCCTACCAAATGTT	19013
rs48936260	snp	C/T			upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733686	GGGCGCTCCAAGAAT[C/T]CCAACTGTCATTTTT	19013
rs48940758	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85729225	CACACCATGAGGAAC[A/G]AAGTTTCCTTCTCTA	19013
rs48953679	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85767995	TTAATCCCAGCACTC[A/G]GGAGGCAGAGGCAGG	19013
rs49036893	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85752381	TCTGTGTTATACCAT[C/T]ATGTGGATGCCAAGC	19013
rs49047458	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85728811	CCAGCCTAGAACAGC[A/G]TAGCCCAAGATAATG	19013
rs49070783	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85751108	AATTTAAAAAAAAAT[A/T]TTTTTTAAAGTCTGA	19013
rs49074006	snp	A/C			intron-variant	Ppara	GRCm38.p3	15:85755794	TTGTGCATGGCTGTC[A/C]CTAACCTCAGGTATG	19013
rs49084972	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85780218	CCCCGTGCTGGGAAC[C/T]CAACTTGGATCCTCT	19013
rs49176398	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85730876	ACAACTCTCAGGCTA[A/G]TGGTCATCACAATAT	19013
rs49183024	snp	A/G			utr-variant-3-prime	Ppara	Mm_Celera	15:85804446	AGGAGTTTCCACTAG[A/G]AAAATCAGGAACTCC	19013
rs49192144	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85731362	GAAGCTGGCTGGGTC[C/T]CTTTGTCATGTCGAA	19013
rs49199463	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85732815	GAGGCCACTATCCTG[A/G]CAGATGACACAGGAT	19013
rs49214846	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85782319	GACTGTTTATTTTTT[A/G]CCTCTTTGCAAATGC	19013
rs49241167	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85800635	GGAAAAAAAAATCTC[A/G]TTGATTTTGTCATGC	19013
rs49291902	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85768402	ATTCAGCAGCATGAG[C/T]CTCTCCCCAACAGTC	19013
rs49305123	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85795457	TTGGTGGAACCAGAT[C/T]GTGTGGAAGGCAGGT	19013
rs49346437	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85766412	AGATAATACAGGTTG[C/T]ATACAGTCCTAGAAA	19013
rs49376827	snp	A/C			upstream-variant-2KB	Ppara	Mm_Celera	15:85727864	TGTCCTCTGGCTTGC[A/C]CACATATACTTGCAG	19013
rs49403956	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85728675	AGGCAAGCTCTTCCC[C/T]ATCTGATGAGAGAAG	19013
rs49406659	snp	C/G			intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85736195	TGAGTCAACAGCAGC[C/G]GACCCTCTTTGAACA	19013
rs49406982	snp	C/T			upstream-variant-2KB	Ppara	Mm_Celera	15:85728168	GTTAATTTCAACCCC[C/T]GCCCCGCCCCCCCAG	19013
rs49431675	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85731470	AAATGTTGGGGTCCA[A/C]GGCGTGAGCTACCAC	19013
rs49466269	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85766988	ACGGGAGGAAAACTC[A/G]ATGACTGTGCATTAG	19013
rs49474947	snp	A/G			upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733871	TGGAACTCAGGACCT[A/G]CAACCAAGCACCCTC	19013
rs49544204	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85729094	GGTCCCAGGCCGTTC[C/T]CCAGCCAGGTAACCA	19013
rs49605814	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85759264	AAACAAAGAACCCTG[C/T]ATCTTCTGGATTTGG	19013
rs49637686	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85768471	GAATTGATAGCACTC[A/T]GCCAGGCGTGGTGGC	19013
rs49641951	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85758429	TGTCTCAAACAACAA[C/T]AATAATGCGGAATCA	19013
rs49644385	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85728938	ACTCTCTGAAAGCAG[C/G]AGCTCAGCCCTTGGT	19013
rs49686967	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85756574	TGCCTTATGAGTCTC[C/T]ATAAGCCTTCTAAGT	19013
rs49721951	snp	G/T			intron-variant	Ppara	GRCm38.p3	15:85766991	ggaggaaaactcaat[G/T]actgtgcattagcaa	19013
rs49745583	snp	C/G			intron-variant	Ppara	GRCm38.p3	15:85750492	TGGTGTGAGTGGCAG[C/G]CCAGCGGTCATGCTA	19013
rs49753462	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85748739	AGGGGTGAGATGTTC[A/G]GGGTTGCTATTATGG	19013
rs49754392	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85796101	ACCAGAGCCCAGTGT[A/C]TGACCACCTCCTTAA	19013
rs49810835	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85763116	CTAGAAGAGAGGCCA[A/G]AAAAAGAACCAATCA	19013
rs49860300	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85758192	GGTGTAACTCTTACA[C/T]AGTGAACAATCGCCA	19013
rs49863138	snp	A/G			utr-variant-3-prime	Ppara	Mm_Celera	15:85805868	TCACCGATACCTGGA[A/G]TTCTCTAATCCAGGG	19013
rs49887416	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85748637	TGGCAGGGGGAGCTA[G/T]CGATGGCCAAGGAGA	19013
rs49892317	snp	C/T			utr-variant-5-prime	Ppara	Mm_Celera	15:85728360	TCCTTCTCCTGGGCC[C/T]GGGACAGGTTAGGAC	19013
rs49940001	snp	C/T			intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770028	CTGATGTCACAGACA[C/T]TGTCACCACACCCTG	19013
rs49950699	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85732631	TTTGTTTCCTGGATG[G/T]TGAGTGCCAGTCCTA	19013
rs50028618	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85782333	TACCTCTTTGCAAAT[A/G]CTGATAATTTGTTTC	19013
rs50053557	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85749995	GATCTAAGCACATAC[A/T]TGACATGGATGGGAG	19013
rs50064118	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85796419	ATCCTGGCTGAGTGC[A/G]CATTTGTCTCTTGGG	19013
rs50155697	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85797281	GGCAGTACACACTTG[A/T]CATCACTGAGCCACC	19013
rs50166151	snp	A/G			intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85769969	TCTTTGCCGTAGTTT[A/G]TGAGACAGTCTCTCA	19013
rs50208661	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85779520	AATTTTTTACATACA[C/T]ATCAAAGTTCCTTTC	19013
rs50224961	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85779661	GCTCAGCTCCGTCCT[C/T]CCCTTTCTTTCACTG	19013
rs50235944	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85780321	AAAAATAAATTGTTT[C/T]TAATTCTATGTGCAT	19013
rs50358503	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85752895	CATCCCTAGGCAGAC[A/G]GGCTTAGAATATATA	19013
rs50420342	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85748788	CCTTCCCTGCGTGAG[A/G]CTGGTGTGAGGAGGA	19013
rs50429785	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85750041	GGTGGGAGGCAAGTG[C/T]GTGGGGTTGGGGGTA	19013
rs50436125	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85750263	GGGAGAACAGCCAGC[C/T]ACTGCTGGAGATGTG	19013
rs50460267	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85800070	GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCGA	19013
rs50473423	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85795345	CATACATCTTTGTAC[C/T]ACATGTGTGCAGTGC	19013
rs50488864	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85797284	AGTACACACTTGTCA[C/T]CACTGAGCCACCTCC	19013
rs50508101	snp	A/G			upstream-variant-2KB	Ppara	Mm_Celera	15:85727690	GCCAGGCATGGTAAT[A/G]CACCTTAGAATCCCA	19013
rs50541743	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85728928	GATGGAAATCACTCT[C/T]TGAAAGCAGCAGCTC	19013
rs50570523	snp	A/G			upstream-variant-2KB	Ppara	GRCm38.p3	15:85727337	TTGTGCTTTTCCTCC[A/G]CAGTGTATGGCAGAC	19013
rs50575389	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85780634	ATTCTTCCAATTGGT[C/T]CCTGAAAGAAGGGTT	19013
rs50584261	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85800069	GGAGGCAGAGGCAGG[C/T]AGATTTCTGAGTTCG	19013
rs50597118	snp	A/G/T			intron-variant	Ppara	GRCm38.p3	15:85763305	GTGACCTGGCGCAAC[A/G/T]CATGGCCGTGCTCCT	19013
rs50603175	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85795510	TCTCTCCAGCCCCAC[A/G]ATGAGCCGTCTTTAC	19013
rs50620787	snp	A/G			upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733860	ACTCTGATCTTTGGA[A/G]CTCAGGACCTACAAC	19013
rs50622489	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85768020	GGCAGGCAGATTTCT[A/G]AGTTGGAAGCCAGCC	19013
rs50634995	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85750479	CCACATAAATGCCTG[A/G]TGTGAGTGGCAGCCC	19013
rs50636402	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85740090	AGAAGCATCTGGATA[C/T]AGCAAGAAAGGTGTG	19013
rs50642269	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85757899	TGTGTGTGTGTGTGT[A/G]TACACGCGTGCACCT	19013
rs50644217	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85756160	AGACACACCAGAAGA[A/G]GGTGTCAGATCTCGT	19013
rs50670050	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85749667	TCTATGAGTTCGAGG[C/T]TAGCCTGGTCTACAT	19013
rs50677558	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85752269	AGGAAAGGCCAAGAG[G/T]ATGGAGCCAATAAAA	19013
rs50685062	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85749951	AAAGGCACAAAATAT[C/T]CCATATTTCCCCTCA	19013
rs50698629	snp	A/C			intron-variant	Ppara	GRCm38.p3	15:85766945	ATTCCAATGCAAAGT[A/C]TAAAGCAGTATAGCT	19013
rs50747375	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85751091	CCATACACATCAACA[C/T]AAATTTAAAAAAAAA	19013
rs50756879	snp	A/G			upstream-variant-2KB	Ppara	Mm_Celera	15:85727611	AAGCAAGTATAGAGC[A/G]ATAGGTCAGTCAATG	19013
rs50787326	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85767600	GGAAAGGGAAATGAC[A/G]CAGACACTGGAAAAC	19013
rs50793618	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85778318	GTGAACACTGGAGCT[A/G]TGGGCAGGTCTGGGC	19013
rs50826141	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85762479	CCTGGTACCCCAGAC[A/T]GGATGGGTAAAGACA	19013
rs50827094	snp	C/G			intron-variant	Ppara	GRCm38.p3	15:85768808	TCACCATCTGGCTAG[C/G]GTAACCATGGGATCC	19013
rs50837224	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85731845	ACCTAGACTCTCACC[A/G]TAGCCAGCAAGTCAC	19013
rs50841500	snp	A/G			intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770024	AGCACTGATGTCACA[A/G]ACATTGTCACCACAC	19013
rs50845149	snp	A/C			intron-variant	Ppara	GRCm38.p3	15:85762995	GCCCTCAGGGAGGGG[A/C]GGGGAGACAGTGTTC	19013
rs50890745	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85780963	GAGGTCCTGAGTTCA[A/G]TTCCCAGCAACCACA	19013
rs50911939	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85778970	TCAGGCTTTCTCTGT[A/G]TAGCCCTGGCTGTCC	19013
rs50956652	snp	A/G/T			intron-variant	Ppara	GRCm38.p3	15:85751836	AATTATAAAGCATGT[A/G/T]TGAGAAAAACACTAC	19013
rs51006701	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85758198	ACTCTTACATAGTGA[A/G]CAATCGCCATCCATC	19013
rs51013128	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85732697	ACTGAAGTCCACCCC[A/G]GGCCACCAGCAAGCC	19013
rs51043104	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85751734	AAGAAAAATGAAACT[C/T]ATCCGTCCTGGGGAG	19013
rs51049469	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85750934	GTTACAGACACTGGC[C/T]GTTCTTCCACAAGAC	19013
rs51099965	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85796463	TCGCTATGTGAATGC[A/G]TCATCTCGCAGCTAA	19013
rs51114703	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85752087	CTGACCAAATGTGTG[C/T]GGGGGGCTGTGCAAG	19013
rs51126745	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85784878	CACATCAATCTTGGC[A/T]ACTTCCAGCTCTTAG	19013
rs51131119	snp	A/G			utr-variant-3-prime	Ppara	Mm_Celera	15:85804444	AGAGGAGTTTCCACT[A/G]GAAAAATCAGGAACT	19013
rs51163757	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85749874	GATATTGGAGTATAC[A/G]TGGGAAAGGATGGGG	19013
rs51189518	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85785103	TCTCACTCTAGCTAC[C/T]CCGGTGCACAGACCA	19013
rs51202864	snp	G/T			intron-variant	Ppara	GRCm38.p3	15:85749950	GAAAGGCACAAAATA[G/T]CCCATATTTCCCCTC	19013
rs51255248	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85749350	AAGCTAAAAGTAGAA[C/G]TGCGGTGTGGGTGTG	19013
rs51348574	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85762456	GAAGCTGAGTATGTG[C/T]GAGCATGCCTGGTAC	19013
rs51439827	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85782311	AGAGGGAGGACTGTT[C/T]ATTTTTTACCTCTTT	19013
rs51474987	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85757086	ACAGTGTCTAGGGCT[A/G]GAGAGATGGCTCAGC	19013
rs51487941	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85800094	AGTTCGAGGCCAGCC[C/T]GGTCTACAAAGTGAG	19013
rs51520347	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85750200	CCACAATAAATGAGA[C/G]GAGAGGACACCAGTG	19013
rs51574662	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85750585	GATTGAGAGACCCTG[C/T]CTCAATGAAAAGGCA	19013
rs51579508	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85763304	AGTGACCTGGCGCAA[C/T]ACATGGCCGTGCTCC	19013
rs51607914	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85729577	AGCTTACCTAGTGTG[A/G]ATTAGTAAACCGGCC	19013
rs51615949	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85742693	AGGGTCTTACTCTCC[A/G]CCCCCTCGCTTTCTA	19013
rs51649491	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85757676	CATCTGCACTGGTGG[A/G]CTCTTCAATAGATCC	19013
rs51657872	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85766712	CAACTCAGCAACCCC[A/T]GAAAAAGCATTTGAT	19013
rs51662294	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85750047	AGGCAAGTGCGTGGG[G/T]TTGGGGGTAGTGTGG	19013
rs51690148	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85759288	GATTTGGCCCTCTTT[A/G]TCAGGTTGGCCTGTG	19013
rs51711696	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85796173	AACTCCTCATGAAAC[G/T]CGTAAGGTATCTGGA	19013
rs51750002	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85751849	GTGTGAGAAAAACAC[C/T]ACCCCTGAAAGATAC	19013
rs51752591	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85778572	CATCGGTAAACCGAC[C/T]TTAGCCATCTTGTGG	19013
rs51766493	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85748573	CAGCTGACCCTCCCT[C/G]GGGAAGGTGTGGAAC	19013
rs51810333	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85794027	TTCCAATGCATGTTT[A/G]TCCTGTCAAATACTC	19013
rs51833449	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85768047	AGCCTGGTCTACAGA[A/G]TAAGTTCCAGGACAG	19013
rs51899925	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85756273	CTCACCAGCCCCCCA[C/T]GTTAGTTTTTTGATA	19013
rs51910793	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85797233	TGCCCATCATAGATA[C/T]AGGAAACTGAACTCT	19013
rs51936091	snp	C/G			intron-variant	Ppara	GRCm38.p3	15:85766833	AATACACAGTGCTGT[C/G]TGTGTGTGTGTGTGC	19013
rs51983265	snp	G/T			upstream-variant-2KB	Ppara	Mm_Celera	15:85728160	TGCCTTCTGTTAATT[G/T]CAACCCCTGCCCCGC	19013
rs51983802	snp	C/T			utr-variant-3-prime	Ppara	Mm_Celera	15:85804477	CTACAGCTGCTCACC[C/T]AGCATAGAGAGTAGG	19013
rs52132273	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85738119	AGCAAGAAAGGAAGG[A/G]AGGAAGGAAGGAAGG	19013
rs52168634	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85738126	AAGGAAGGAAGGAAG[A/G]AAGGAAGGAAGGAAG	19013
rs52185729	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85767371	ACACACACACACACA[C/T]ACACACACACACACA	19013
rs52222185	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85738056	TAGTTCCCCAATAGC[C/T]AGGGCTACACAGAGA	19013
rs52326857	snp	G/T			upstream-variant-2KB	Ppara	Mm_Celera	15:85727003	CAAAAAACCAAAAAT[G/T]AAATAATAAAAATAG	19013
rs52364988	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85780595	ACACGGTCAGTTTGG[A/G]GAGAACTGACATCTT	19013
rs52374033	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85749749	ACAAAGCAAAGCAAA[A/G]CAAAACAAAACAATA	19013
rs52404666	snp	A/C			upstream-variant-2KB	Ppara	GRCm38.p3	15:85727043	AAAATAAAATAAAAT[A/C]AAAAAAACTAAGCTT	19013
rs52419437	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85738472	AAGAAAGAAAGAAAG[A/T]AAGTTAGTTGAAGGC	19013
rs52428109	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85793748	TCAGAGCTAGAATTA[C/T]AGACATTGTGAGCTG	19013
rs52436475	snp	A/T			upstream-variant-2KB	Ppara	Mm_Celera	15:85727042	TAAAATAAAATAAAA[A/T]AAAAAAAACTAAGCT	19013
rs52453412	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85757486	AATCATACACACGTG[C/T]GTACACACACAAACA	19013
rs52467649	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85738412	AAGAAAGGAAGAAAG[A/G]AAGAAAGAAAGAAAG	19013
rs52473953	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85795209	tgtgtatgtgtgtgt[A/G]GCCTACCTTGTTCTG	19013
rs52581805	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85738495	TTGAAGGCTAGGGCT[C/G]TAGTTCAGTTGGAGG	19013
rs52587137	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85748839	TAGGGTGTGAGTGAA[C/T]GGGGAAGGCAGGGGT	19013
rs52705448	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85745883	TGTGTGTGTGTGTGT[A/G]TGTGTATGTTAAGTG	19013
rs52705516	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85749700	CAAGTTCCAGGACAG[C/T]CAGGGCTACAAAGGG	19013
rs52705518	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85749706	CCAGGACAGCCAGGG[A/C]TACAAAGGGAAATTC	19013
rs52705522	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85749707	CAGGACAGCCAGGGC[A/T]ACAAAGGGAAATTCT	19013
rs52705524	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85749720	GCTACAAAGGGAAAT[C/T]CTGTCTCAAAAAAAC	19013
rs52705530	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85750610	AAGGCAGAGAAGCAA[A/T]TGAGGATGATAGCCA	19013
rs52705532	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85750628	AGGATGATAGCCAAC[C/T]GTAGTGTCAGGCTTC	19013
rs52705534	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85750635	TAGCCAACTGTAGTG[C/T]CAGGCTTCCACATGC	19013
rs52705536	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85750649	GTCAGGCTTCCACAT[A/G]CATATGGACCCATGC	19013
rs52705540	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85751203	GACTGGTCTACAGAG[A/T]AAGTTCTAGGATAGC	19013
rs52705546	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85753297	TGATGATGGTGACGA[C/T]GATGAAGAAGATAGA	19013
rs52705556	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85755954	TTCTTGTTGGTGTGT[A/G]TGTGTGTGTGTGTGT	19013
rs52705558	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85755993	ATGTTATACACATGT[G/T]TGTATATGCATGTGT	19013
rs52705560	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85756053	TCTGCAGAGGTGAGA[A/G]GTCAGTGTTCCTCCT	19013
rs52705562	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85756058	AGAGGTGAGAAGTCA[A/G]TGTTCCTCCTTCTAC	19013
rs52705564	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85756127	TTTATTGTATGTAAG[C/T]ACACTGTAGCTGTCT	19013
rs52705566	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85756142	CACACTGTAGCTGTC[C/T]TCAGACACACCAGAA	19013
rs52705568	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85756151	GCTGTCTTCAGACAC[A/T]CCAGAAGAAGGTGTC	19013
rs52705696	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85758499	ATACATAAATTCCTT[C/T]ATTTGAGTTAATCCT	19013
rs52705706	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85762143	TATATATATATATAT[A/G]TGTGTGTGTGTGTGT	19013
rs52705729	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85768063	TAAGTTCCAGGACAG[C/T]TAGGGCTACACAGAG	19013
rs52705733	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85768674	TGTGTGCATTGTGTT[A/G]TGTACACACACATAC	19013
rs52705737	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85768745	CCTGAGGTGTTTACC[A/G]CTTTACAACTTGCTT	19013
rs52705873	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85772715	TCTGTCTGTCTGTCT[G/T]TCTTTCTCTCTTTCT	19013
rs52705875	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85772742	TTCTTTCTTTCTTTC[C/T]TTCTTTCTTTCTTTC	19013
rs52705885	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85778688	CCATCTTGAGGGGAG[C/T]CATGGTGCTTCAAGG	19013
rs52705887	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85778756	TTTATTTATTTATTT[A/G]TTTATTTATTTATTT	19013
rs52705889	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85778760	TTTATTTATTTATTT[A/G]TTTATTTATTTATTT	19013
rs52705891	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85778800	AAGTACACTGTAGCT[A/G]TCTTCAGACACTCCA	19013
rs52705903	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85781021	ATCCAATGCCCTCTT[C/T]TGATGTGTCTGAAGA	19013
rs52705905	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85784605	AATTTGGGgtgtgtg[A/T]gtgtgtgtgtgtgtg	19013
rs52705995	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85794875	TAGGGCTTCTCACAG[G/T]AGTCCGTCTTCTTGT	19013
rs107703182	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85756462	GAAAATTCCATTTTC[C/T]CCCCAAAATGTATTG	19013
rs108089523	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85781099	CATGGAAATCTTTTT[A/T]AGAAAGACTTATTTA	19013
rs108122852	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85743664	GGTTGGCAGTGTCTG[A/G]GGCATTTAGCTGAAG	19013
rs108203359	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85794952	CAAACACTTTTACCC[A/G]CCAAGCCATCTCACC	19013
rs108383029	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85781345	CAACAGTGTTCTTAT[A/G]GGGTGCTTAGATACT	19013
rs108490420	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85781131	GAATAATGATGTCAT[A/G]TGCCACAAAGACAGT	19013
rs108784533	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85781125	CCATGTGAATAATGA[C/T]GTCATATGCCACAAA	19013
rs211700087	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85761360	ttagctgtattcccc[A/G]gctgtattccttaac	19013
rs211737112	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85782484	TAGGTTGCCTTACAC[A/G]ATTGGAGGCTGGGTG	19013
rs211784285	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85766363	CCCTGCACCAAATGA[C/T]TCACTGGAGAATTGG	19013
rs211799102	snp	A/G			intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85775526	GGATTCAGCTAGGTT[A/G]GCTGACCAGCCTGTC	19013
rs211827165	snp	C/G			upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733210	TTATACCCCAGGATA[C/G]ACCAACACATTTGCA	19013
rs211863562	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85741557	tatatatatatatat[A/G]tgtgtgtgtgtgtgt	19013
rs211909348	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85798795	GGGAAGCTGGCGGCA[C/T]GGTCCCCGATGTTTG	19013
rs211945442	snp	C/T			intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85774438	GGCCACTCTTCTCCA[C/T]GAATCAGCAATGGTG	19013
rs211961425	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85743527	GTGATCAACGCAGGA[C/T]GAAGCCACGTATGGT	19013
rs211964768	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85732356	CCACGGCTTTTGAAT[A/T]GTCTGATGCCAACCC	19013
rs212050490	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85799828	TGGGGAGGCGGCTCC[A/G]TGGTTAGGAGCATGT	19013
rs212056403	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85787656	AGCTAGGGCAGAGGT[G/T]ACCATGTGTTGAGCA	19013
rs212076655	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85745644	GTAGTATATACTTGT[C/T]TCTGTGTGTATGTGT	19013
rs212119486	snp	C/T			downstream-variant-500B	Ppara, Cdpf1	Mm_Celera	15:85806946	AGTGTCCAAGTGTCA[C/T]TGAAACAGTGACTCA	19013
rs212133780	in-del	-/T			intron-variant	Ppara	Mm_Celera	15:85758533	TTGTAATTACACTGA[-/T]TTTTTTTTGTTTATT	19013
rs212168258	snp	A/T			intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85735743	AGGGGAGGGGCTCGG[A/T]GGCGCATGCGCGCGG	19013
rs212191275	in-del	-/AC			upstream-variant-2KB	Ppara	Mm_Celera	15:85727893	GCCATACCCACAGGG[-/AC]ACACACACACACACA	19013
rs212191760	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85800907	GAAGGTCCCTCAGTG[C/T]CTCCTCAGCGGGGCC	19013
rs212192258	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85752461	ATCTCCAATGGTAAC[G/T]AGGGCCTTCGGCTCT	19013
rs212209171	in-del	-/TTT			intron-variant	Ppara	Mm_Celera	15:85731618	GGAATTGAGGATTTC[-/TTT]CTTTTTTTTTTTTTT	19013
rs212210055	snp	G/T			intron-variant	Ppara	GRCm38.p3	15:85750498	GAGTGGCAGCCCAGC[G/T]GTCATGCTAGCCTCA	19013
rs212267390	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85794069	AGCCCCTCTCATTGT[C/G]TTGCTCTAAATCTTG	19013
rs212327920	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85760470	AAAGTTATAGTAAGC[A/C]GGGGCCAGGGAGAGA	19013
rs212506643	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85740170	GCGCTGCTGCCACCT[C/T]TCAGCTGCCATCTGC	19013
rs212532299	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85796566	GTTCATTTTAGCTTG[A/C]AGTTTGAGGGTCAGG	19013
rs212532823	in-del	-/TGTGTGTG			intron-variant	Ppara	GRCm38.p3	15:85766830	TTCAATACACAGTGC[-/TGTGTGTG]TGTGTGTGTGCTTGG	19013
rs212534126	snp	A/G			utr-variant-3-prime	Ppara	Mm_Celera	15:85804743	AAAACACTAAAATCT[A/G]CATGGAGAGGTTTTG	19013
rs212579421	in-del	-/GTGTGT			intron-variant	Ppara	Mm_Celera	15:85783875	CACCTGCCACTCATA[-/GTGTGT]GTGTGTGTGTGTGTG	19013
rs212599472	snp	G/T			utr-variant-3-prime	Ppara	Mm_Celera	15:85804331	TTAAAGTTTTCCCGG[G/T]GTCCCCTGAGATTAA	19013
rs212623765	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85752054	CTGAGTCTCTTGCTG[G/T]ACCAGAGGCAGGGCA	19013
rs212658096	in-del	-/GTGT			intron-variant	Ppara	Mm_Celera	15:85793672	TTTAGTCACGTGCAG[-/GTGT]GTGTGTGTGTGTGCA	19013
rs212673217	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85797182	TAGACAAGAGCACTA[A/C]GTCCCCTGGAGCTGG	19013
rs212674242	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85762857	TGGTGTAGGGAGTCG[A/G]GTACAGTGCGGGTGG	19013
rs212682863	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85779656	TCTTTGCTCAGCTCC[A/G]TCCTTCCCTTTCTTT	19013
rs212798350	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85749313	GGCCGCCATCCAGGG[A/T]ACCAGTGTGGCGGTG	19013
rs212859339	in-del	-/TGTGTGTGTGTA			intron-variant	Ppara	Mm_Celera	15:85741592	GTGTGTGTGTGTGTG[-/TGTGTGTGTGTA]TGTAAAATTTCAAGA	19013
rs212876868	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85757810	GGTTACTATTTATTG[C/G]TAGAGATGCTTTGGA	19013
rs212890799	in-del	-/C			intron-variant	Ppara	Mm_Celera	15:85791670	AGAGGGAACAGCCCT[-/C]CCTTGGCACATGAGG	19013
rs212916175	snp	C/T			intron-variant	Ppara	GRCm38.p3	15:85765720	GATTTGGAGTTAAGG[C/T]GGTGAGTTAAGATGA	19013
rs213006088	snp	A/T			utr-variant-3-prime	Ppara	Mm_Celera	15:85805743	TTCTGCACTGAATGA[A/T]AAAGAATGCTCTTCA	19013
rs213027559	in-del	-/GTGTGTGTGT			intron-variant	Ppara	GRCm38.p3	15:85779969	CAGCTGGTCAGTTTA[-/GTGTGTGTGT]GTGTGTGTGTGTGTA	19013
rs213059613	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85764786	GACCAGAGGAAAACT[A/C]AAAACAATGTTTCAA	19013
rs213092834	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85780508	CTGCCTTTTTTTTAA[A/T]AAAAAAAGAAGATGA	19013
rs213198933	snp	G/T			intron-variant	Ppara	Mm_Celera	15:85730403	AGAAGCTGCCAGATT[G/T]GGGGGGGGGCAGGGA	19013
rs213211415	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	Ppara	Mm_Celera	15:85771409	CATCGATCTGTGGCT[C/T]CTGTCACCTGGCTGC	19013
rs213247530	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85762282	CAATTCACTTTGAAA[C/T]TATGTAAACAGCGCT	19013
rs213262259	in-del	-/TCTTA			intron-variant	Ppara	Mm_Celera	15:85759282	TTCTGGATTTGGCCC[-/TCTTA]TCTTTATCAGGTTGG	19013
rs213288887	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85731268	ATGTGTGAAATATTT[A/C]TTTCCATTTAGTGTT	19013
rs213370679	in-del	-/A			intron-variant	Ppara	GRCm38.p3	15:85767223	CAAATCACCCAGAGT[-/A]AAAAATACCTAAGCT	19013
rs213390504	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85758392	ACTGCTATTTTTTGG[C/T]AGGGTTACATAGTTG	19013
rs213397969	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85761687	ATCCCAATGTATCTG[C/T]ATCCGGATAGACAAT	19013
rs213447855	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85767820	CATTACTACATAGAT[A/G]AATATTTTAAAAACG	19013
rs213585434	in-del	-/A			intron-variant	Ppara	Mm_Celera	15:85751422	TTTGGAAAATATTTG[-/A]AAAAAAAATCAAGGA	19013
rs213587303	in-del	-/A			intron-variant	Ppara	GRCm38.p3	15:85743297	AACAAACAAACAAAC[-/A]AAAAAAACCAAAAAA	19013
rs213598257	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85793833	TTAACTGCTGAGCCA[C/T]CCCTCCAACCCCATA	19013
rs213611687	in-del	-/TT			intron-variant	Ppara	Mm_Celera	15:85796357	GGCATCTTTTTTTTT[-/TT]AATGGCTAATATTCT	19013
rs213724792	snp	A/T			intron-variant	Ppara	GRCm38.p3	15:85781100	AAATAAGTCTTTCTA[A/T]AAAAGATTTCCATGT	19013
rs213747800	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85784004	CCCTGGTTTGTTTTT[C/T]CACACCACGTATTGT	19013
rs213764905	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85769258	AGCCATGCCGCCATC[A/T]CCCACACCACCAATG	19013
rs213770181	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85746072	GAGAACGGCTCTCTC[A/G]GAATCTAGCGCTTAT	19013
rs213781058	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, intron-variant	Ppara	Mm_Celera	15:85735562	ACAGGGGTGACGGGG[A/G]CGGAGGCAGCCGCTT	19013
rs213786524	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85761239	CTTATACTGTGGCCT[C/T]GGGGGTCAGATTTTC	19013
rs213798801	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85739044	AAACATCAGTTGAAA[C/T]GTGTCTTTGCTTGTC	19013
rs213812086	snp	A/T			intron-variant	Ppara	Mm_Celera	15:85772651	TAATAATACAGAGGT[A/T]TGGCGATGGGTCCAA	19013
rs213875145	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85746953	CTGGCCAGCGGGTCA[C/G]TGGCTTCCTGAGATG	19013
rs213909363	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85795316	ATTTCATGAGTATGG[A/G]TACTTTTCCCACACA	19013
rs213928329	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85737415	GGAGCCTGCGATGTA[A/G]CCCATGCTAGCCTGG	19013
rs213934211	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85747575	ATCTCAGATTCCAGC[A/G]GGCAGGAGTTAGAGT	19013
rs213982940	snp	C/T			utr-variant-3-prime	Ppara	Mm_Celera	15:85803013	tcaaacccacttgcc[C/T]cctttgtcttccctc	19013
rs214002345	snp	C/T			utr-variant-3-prime	Ppara	Mm_Celera	15:85803396	CTTGCTGTGTGCCTT[C/T]AGCATGGACCAACTG	19013
rs214024759	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85783208	TTGGTCGTATCACAT[C/G]AATTACAGGAAGGGA	19013
rs214137376	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85773527	CTCAATTTATGACTG[A/G]GACCTTCTCTGTTCA	19013
rs214167255	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85742988	AGGAGCCTAAAGTCC[C/T]TGAAATTTCAGATTG	19013
rs214186397	in-del	-/T			intron-variant	Ppara	Mm_Celera	15:85799064	GTCTGTGTGTGTGTG[-/T]GGGGGGTCCCCTTTG	19013
rs214235665	snp	A/G			upstream-variant-2KB	Ppara	Mm_Celera	15:85726697	AGGAAGGGTGTCACT[A/G]GGCTGTGGGCTTTGA	19013
rs214278066	in-del	-/A			intron-variant	Ppara	GRCm38.p3	15:85781784	GTCTAAGATTTTATT[-/A]AAGGGGGTGTTGGTT	19013
rs214374164	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	Ppara, Cdpf1	Mm_Celera	15:85806499	GGAATTATTGAGCCG[A/G]TACCAGCATCCCCAC	19013
rs214383735	snp	G/T			splice-donor-variant	Ppara	Mm_Celera	15:85728387	GGACAAGCAGATAGG[G/T]AAGTCCTGGTGTTTG	19013
rs214432967	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85743562	TACGCCTATAATCCG[A/C]ACTGGGGAATCTAAG	19013
rs214433050	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85752007	GCCTGTTGGGGAAAG[C/T]AAGGGACCCTTTCAC	19013
rs214437471	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85789435	AATTCATTCATTCAT[C/T]CATTTAGCTTTTGAG	19013
rs214460119	in-del	-/TTA			intron-variant	Ppara	Mm_Celera	15:85759919	TTTGTTGATTTTTTT[-/TTA]AACTTAATTGATTGC	19013
rs214481002	snp	C/G			intron-variant	Ppara	Mm_Celera	15:85731482	CCAAGGCGTGAGCTA[C/G]CACATCTGGCATGAA	19013
rs214496595	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85787631	TGACCTCAGGACCTC[C/T]CCAGAGGCCAGCTAG	19013
rs214557638	in-del	-/GCGGGGGG			intron-variant	Ppara	Mm_Celera	15:85752085	ACTGACCAAATGTGT[-/GCGGGGGG]GTGGGGGGCTGTGCA	19013
rs214564975	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85751206	TGGTCTACAGAGTAA[A/G]TTCTAGGATAGCCAG	19013
rs214582796	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85800782	GGCTGCACCGTAAGG[A/G]GGTGTGGGGTAGGAC	19013
rs214648975	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85742362	GGATGCGCCCAATTC[C/T]GAAACACACCAAGTC	19013
rs214662696	snp	A/C			intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85774371	GGTTTCTTCCTCATT[A/C]CCCTACCGTTCTGGA	19013
rs214744712	snp	C/T			synonymous-codon	Ppara	Mm_Celera	15:85797944	CTGCCAGTGCATGTC[C/T]GTGGAGACCGTCACG	19013
rs214825742	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85747786	TCCGTAGAGTACCAG[A/G]GCGGCCCTGCTGTGT	19013
rs214834312	in-del	-/A			intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85769480	CAAAGAGAGGTACAT[-/A]CCGAATGTTGCCGAA	19013
rs214870142	snp	C/T			intron-variant	Ppara	Mm_Celera	15:85759261	CAAAAACAAAGAACC[C/T]TGTATCTTCTGGATT	19013
rs214931322	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85732271	GGCTTCCTGGGCAGG[A/G]CCCCACCCACCTCTG	19013
rs214934271	in-del	-/TCCACCC			intron-variant	Ppara	GRCm38.p3	15:85781865	TGTAAAAGGAGGAAA[-/TCCACCC]CCCCCCCTTCTCTTT	19013
rs214947037	snp	A/C			intron-variant	Ppara	Mm_Celera	15:85760337	ATTTTAAAAGTATTA[A/C]AGTTTACTTACTGGC	19013
rs214967674	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85755581	GGAAGTAGACGGAGC[A/G]TTATGGCCAGAGTCT	19013
rs215075046	snp	C/T			upstream-variant-2KB	Ppara	Mm_Celera	15:85726377	CTACACCCAAGGTAC[C/T]TCGAGGAAGAACCAC	19013
rs215114788	snp	A/G			intron-variant	Ppara	Mm_Celera	15:85757714	TTGCTGTGGATTAGC[A/G]TTCTGTATTGCACTG	19013
rs215199133	snp	A/G			intron-variant	Ppara	GRCm38.p3	15:85765861	GACCTTCGTGTGCAC[A/G]CTCTTTTGCATATAC	19013
rs215266419	snp	A/C/T			intron-variant	Ppara	GRCm38.p3	15:85730825	aagaagaagaagaag[A/C/T]AGCAGCTTTCTAGAG	19013

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