SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3697592 | snp | A/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115469200 | CAATGTAAACTAGAT[A/T]AAAAAAAAAAATTAC | 19016 |
rs3698220 | snp | A/G | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115469306 | TGCTAGGGCTCTCTT[A/G]GCTTTGTATAGAAAT | 19016 |
rs3698385 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Pparg | Mm_Celera | 6:115469385 | AAGGCTGTCAGTGAT[C/T]CAGAGTGTTAATAAC | 19016 |
rs3699371 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Pparg | Mm_Celera | 6:115469494 | ATGCCTAAGTGGATC[C/G]TTTGAAGTATGGGAA | 19016 |
rs6211345 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Pparg | Mm_Celera | 6:115464041 | TAGATGAAAATTATC[A/G]TTGAATCCAGTTTTC | 19016 |
rs6211421 | snp | C/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115464085 | GCTTCTGATAGGAAG[C/T]TGAGAATCAACNTCA | 19016 |
rs6211793 | snp | A/G | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115464097 | AAGNTGAGAATCAAC[A/G]TCAAATTACATTAAA | 19016 |
rs6340867 | snp | A/G | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366658 | taccactttgtctgg[A/G]ttcctagagaggctg | 19016 |
rs6341382 | snp | A/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366801 | ctgagccatttctct[A/T]gccccATCTTATTCT | 19016 |
rs6341821 | snp | A/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366854 | TATATTTAACTACTT[A/T]AAAAAAAAACCTATA | 19016 |
rs6341880 | snp | C/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366884 | AGACTTATCTGGAAT[C/T]CTAANATGGAGATAA | 19016 |
rs6341892 | snp | A/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366889 | TATCTGGAATNCTAA[A/T]ATGGAGATAAAATGA | 19016 |
rs6342353 | snp | A/G | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115366950 | AGTTCAGATTGGCAT[A/G]GACCTGGNAGTGAGG | 19016 |
rs6342369 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Pparg | Mm_Celera | 6:115366958 | TTGGCATNGACCTGG[A/G]AGTGAGGAGTCCTTT | 19016 |
rs6350947 | snp | C/G/T | 0.456747 | 0.140554 | intron-variant | Pparg | Mm_Celera | 6:115418086 | CTCTCAGTGTGTTTT[C/G/T]GGGTATTGTAAACAA | 19016 |
rs8236549 | snp | A/G | 0.4032 | 0.19756 | synonymous-codon | Pparg | GRCm38.p3 | 6:115473037 | AAGGTTAATGAAACC[A/G]GGGATATTTTTGGCA | 19016 |
rs8236550 | snp | A/G | 0.470416 | 0.117969 | synonymous-codon | Pparg | GRCm38.p3 | 6:115473055 | CACTTGGTCATTCAA[A/G]TCAAGGTTAATGAAA | 19016 |
rs8239553 | snp | A/T | 0.21875 | 0.248039 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360545 | TTCGCCTTCATAACA[A/T]TCTGAGATtaaaaat | 19016 |
rs8239554 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360572 | aaataaaaataaaac[-/T]nagattaaaaataaa | 19016 |
rs8239555 | in-del | -/G | 0.5 | 0 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360573 | aataaaaataaaacn[-/G]agattaaaaataaaa | 19016 |
rs8239556 | in-del | -/A | 0.444444 | 0.157135 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360592 | ttaaaaataaaaann[-/A]nannngaaaAAAGGG | 19016 |
rs8239557 | in-del | -/A | 0.444444 | 0.157135 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360593 | taaaaataaaaannn[-/A]annngaaaAAAGGGA | 19016 |
rs8239558 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360619 | AGGGAGATCCTAAAT[A/T]CACTTAATTCatata | 19016 |
rs8254771 | snp | A/G | 0.35503 | 0.226867 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360159 | CTGAAAGAGTGCAAG[A/G]AAAGGAACTGTCTAT | 19016 |
rs8254772 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360200 | TCAGGCTCCCGAGGC[A/C]AGAAGCTCCAATAGT | 19016 |
rs8254773 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360201 | CAGGCTCCCGAGGCA[A/G]GAAGCTCCAATAGTC | 19016 |
rs8254774 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360376 | GAACACTTTGTGTTC[G/T]TCCAGAGGACCCTTG | 19016 |
rs8254775 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360388 | TTCTTCCAGAGGACC[C/T]TTGTTCGGTTCCCAG | 19016 |
rs8254776 | snp | A/C | 0.132653 | 0.220748 | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360444 | CAGGGGAGCCCACAC[A/C]TCTCCCTCCGTTCAC | 19016 |
rs8254777 | snp | A/T | 0.391111 | 0.206368 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115361271 | CTGAGGAGAAGTCAC[A/T]CTCTGACAGGAGCCT | 19016 |
rs8254778 | snp | A/G | 0.444444 | 0.157135 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115361295 | GGAGCCTGTGAGACC[A/G]ACAGCCTGACGGGGT | 19016 |
rs8254779 | in-del | -/A | 0.142012 | 0.225474 | frameshift-variant | Pparg | Mm_Celera | 6:115473164 | ACTCCCTGGTCATGA[-/A]TCCTTGGCCCTCTGA | 19016 |
rs8254780 | snp | A/G | 0.336735 | 0.234472 | synonymous-codon | Pparg | GRCm38.p3 | 6:115473001 | TGTGATCTCTTGCAC[A/G]GCTTCTACGGATCGA | 19016 |
rs8254781 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon | Pparg | GRCm38.p3 | 6:115472953 | AATTCGGATGGCCAC[C/T]TCTTTGCTCTGCTCC | 19016 |
rs8254782 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Pparg | GRCm38.p3 | 6:115490033 | AGAGGACTCTGGGTG[A/G]TTCAGCTTGAGCTGC | 19016 |
rs29969982 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Pparg | GRCm38.p3 | 6:115422832 | TCAGATTTGCTTCAC[A/G]GGAACAAAATTCTCC | 19016 |
rs30014734 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | GRCm38.p3 | 6:115466553 | GTCACTAAAGAAGTC[C/T]TAGGAACATTATACA | 19016 |
rs45639557 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115382887 | AGTTTTGTGTGTGTC[A/G]GACTGTGCAGAATGT | 19016 |
rs45654618 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115387630 | TAACTTTAATTACAT[A/T]TAGGTATGCATGTGG | 19016 |
rs45687356 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115464460 | ATGACTTCGAGTGGA[A/G]TCAGCTAGTAGCTAT | 19016 |
rs45693233 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Pparg | Mm_Celera | 6:115440075 | ATACCAAAGTATGTT[C/T]ACTTTTCAAACTACT | 19016 |
rs45700899 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115391560 | AACTTCATTTTTCAT[G/T]CTAATTATTGTTACA | 19016 |
rs45722776 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115385772 | GGTAATTCGTACTCA[A/G]ATCAGAGGTATGAGG | 19016 |
rs45722938 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115476896 | GCCAGCTTGCTGAGA[A/G]AGATGACCTAGTTCT | 19016 |
rs45735678 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115378890 | CTAGTTTTATAATAT[C/T]TGTGTTACCAGAGAA | 19016 |
rs45749774 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115387167 | AAAAGAGTGTCTGTT[G/T]ATTAAAGATATCTGA | 19016 |
rs45763130 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | GRCm38.p3 | 6:115402837 | GAGCAGTTAGATGTC[A/G]TTTTTTTAATTTAAT | 19016 |
rs45771868 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115469006 | ATCAGAAAATCTCAT[G/T]CCCAGAGCCTTGGCC | 19016 |
rs45775174 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115414008 | CTGGTTTATTTAAAT[A/C]ATTTAACAATTCTTT | 19016 |
rs45777353 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115453906 | TTCAAGTTTCCAAAG[G/T]AGACACCCTGTGCAT | 19016 |
rs45781199 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115418887 | GAGAACAAGATAGAT[A/G]CATACTTACAGGAAA | 19016 |
rs45787490 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115373963 | TGGATGCAGTATTGA[A/G]ACTCAAACCCAGACC | 19016 |
rs45792435 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115441166 | CCTAGCCAAGTAAGC[G/T]TCACTTATCCAAACC | 19016 |
rs45792522 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115461547 | AAGTCACTGAACAGA[C/T]AGAAATGTTCCTGTA | 19016 |
rs45794401 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115365367 | TTTTCTGTTTTTGTG[A/G]GTCCTTCACAGACAA | 19016 |
rs45804653 | snp | A/G | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115433413 | TAATTGGAGGTTATT[A/G]TTTTTGTTAGTGTAG | 19016 |
rs45806952 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115472724 | TGATAAATAGGAAGA[A/G]CCTCTCTCCTGTTTA | 19016 |
rs45807727 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115371335 | GCTAGGTAAACTGTT[C/T]GCCACTGAGCCACCA | 19016 |
rs45822703 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115388584 | TTACCTGCGTAACTT[C/G]TGATTTGGGGTAGTG | 19016 |
rs45826663 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115436815 | CAGGAAAAGATACAG[C/T]AACCTCAGGAATCTG | 19016 |
rs45826745 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115412182 | AGATAACTTTGGAAG[C/T]ACCAGTTGAATTCAT | 19016 |
rs45826789 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Pparg | Mm_Celera | 6:115372226 | TGTTTCTGTCATGTA[G/T]TATTAAAGTATAGGG | 19016 |
rs45853449 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115397029 | TGTTAGGAGTCTGTA[C/T]ACCTATAAATCAGCA | 19016 |
rs45866169 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115376610 | GTGGTAGGGAGTTCC[A/G]GTTTTGAGAAAAGCT | 19016 |
rs45885522 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115419715 | CACAAGTTAAATGTT[C/G]CTTTTGAAAGGAAGG | 19016 |
rs45887332 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115397830 | GCAGGTGGTTAGTCA[A/G]TGCTTACCCTGTGAG | 19016 |
rs45897754 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Pparg | Mm_Celera | 6:115478595 | GTTCATATACTGTTA[A/C]TGATATCCAATGCCC | 19016 |
rs45911251 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115412728 | AGAGATGATGAAGGT[C/T]TTAGAACCCTAAGCA | 19016 |
rs45911754 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115485874 | TTGCATTTCATTCCC[C/T]GAGCCAGGTTCCAGC | 19016 |
rs45942963 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115424680 | GTTGAGCAATGGAAA[C/T]GCATCTTAGAAACAT | 19016 |
rs45944314 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115394328 | ATAATATATTCCTGG[C/T]TCACGGTTTTGTTTT | 19016 |
rs45956838 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Pparg | Mm_Celera | 6:115490824 | CAAACTTCTCCCACG[A/G]CTCTGAGTTTTCACG | 19016 |
rs45957498 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115421617 | AAGATAAATACTTAA[A/G]AAAAACTTTGGCCAA | 19016 |
rs45982368 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115375552 | TTCATTTATTTCCAA[C/T]TTTAAAATTATAGTA | 19016 |
rs45996004 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420020 | CATTGGTATTGAAAA[C/T]GGGATAATATAGGTA | 19016 |
rs46002291 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Pparg | Mm_Celera | 6:115434259 | ATTAACCTAAAACAA[A/G]AAGTCATTGAAAATT | 19016 |
rs46009770 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115487367 | ACAAGCAGGATATAA[C/T]GATGTGAGTAGGTTT | 19016 |
rs46012115 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115390374 | AATTCAATTGACAAG[A/G]TCTAGTTTTGCTAGT | 19016 |
rs46016286 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115414926 | GTATTAATTGTCCTG[A/G]TACTAAGTTTTATCA | 19016 |
rs46027909 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115396255 | AGCAGCCCGGTGATA[C/T]TGAATAACCTTCTCC | 19016 |
rs46055300 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115443454 | ACATTAATGAGTGTG[A/G]ATTGTATAATCATTC | 19016 |
rs46076755 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115397977 | GGATTCACTCAGAGT[C/T]TAAACGGTCAGTCAG | 19016 |
rs46096787 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115380918 | CTTGCAGAGTATTTA[C/T]ATCTTAATGTCTTCT | 19016 |
rs46096866 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115395245 | CCTGAGATACAACTC[A/G]GAAGCTAGATGGAGC | 19016 |
rs46097543 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115461072 | TTTTTTTAAATGGCA[A/G]TTGTTTAAAGATTTC | 19016 |
rs46124349 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115376493 | ATTACCTAATAGATA[A/G]TAGGCACTCAAATAT | 19016 |
rs46127268 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115455351 | AGGGAAGCTCAGAAT[A/G]CAAGTGCTAACATGT | 19016 |
rs46146082 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115462801 | TAGGAGTTGTCTCTC[A/G]ATTCATGTTTAAATG | 19016 |
rs46160271 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115367372 | TGCTGGGGTGAAGAA[C/G]TGGAAAGAACTCCTT | 19016 |
rs46196029 | snp | G/T | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115479489 | GTTCCCCTTCAGTTC[G/T]TGAGTATACGTGCCA | 19016 |
rs46196758 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115459563 | GATTGGTCTGTGAAG[C/T]AGTAGATGATTCTGG | 19016 |
rs46223269 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115398890 | TTAATATCACAACAC[C/T]GGGGAGCAGACTTCC | 19016 |
rs46223975 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115390269 | ATCATTTTGTATGAG[G/T]CGAGTATTAACAATG | 19016 |
rs46239196 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Pparg | Mm_Celera | 6:115390036 | AATCCAAGAACATGT[A/T]GTGTGGGCTCCTTTT | 19016 |
rs46265991 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115454812 | GTCCTACTCTATGTT[C/G]ATTTGGCCCTGTTGC | 19016 |
rs46274689 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115419586 | ACACAATCCTAGGAG[C/G]AGATGCTACCAGATT | 19016 |
rs46301931 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Pparg | Mm_Celera | 6:115483824 | CAGACCCTTCGATAG[C/T]TTACTTTACTCTGTT | 19016 |
rs46302523 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115388737 | GAGTAGTGTGTTGTC[C/T]TAGTAGGTACAGCAC | 19016 |
rs46306894 | snp | G/T | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115485104 | AGCCTTTCAGGGAAT[G/T]TCCTAGCAGGCCCTG | 19016 |
rs46312450 | snp | C/T | 0.489796 | 0.070696 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115451709 | CCTTTGCTATATTAT[C/T]CTTGACTTCAGAGAA | 19016 |
rs46319133 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115446666 | TGATTTTTACATACA[C/T]AGTCAATATTAGTAA | 19016 |
rs46325420 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115382167 | ATATAACCTGGCCTG[A/C]TGTGAACTTTGTGTC | 19016 |
rs46329925 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115368448 | AATTGGTGGGATTTG[C/T]TAAGAGTGGCCACCC | 19016 |
rs46353648 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Pparg | Mm_Celera | 6:115463602 | GAAGCCTTCCAGTCA[C/T]AAGAGTGTCTCAGAA | 19016 |
rs46363895 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115390885 | GATAAGTCAAGCCAA[C/T]CTTGAAAACAGTAGG | 19016 |
rs46379256 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Pparg | Mm_Celera | 6:115440683 | CAGAACCAAACTTTT[C/T]GAGATAAAGTATCAT | 19016 |
rs46383112 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115405498 | GAATCAAAATTGTTA[A/G]TTTCCTTTCAAGGTA | 19016 |
rs46395238 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115413089 | GAGATCAGATTATTG[C/T]CATTCCATGTTAGTG | 19016 |
rs46404515 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115385864 | TAAATGCAAGCTAAA[C/T]GGATTTCCCCCACTG | 19016 |
rs46432370 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115464820 | CCAAAAGTAGCCATG[A/G]CAAGAGACACACAAG | 19016 |
rs46473968 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115373725 | GAGTGTAACTGAAAT[C/T]AAAGGAGTGAGGGAG | 19016 |
rs46481331 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115363303 | CTATATCTTCAGTGA[A/G]AAGATCTAAGGAGCA | 19016 |
rs46489562 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115407726 | ACCACTAAGCTACAT[C/T]CCTATCTTGCATGTA | 19016 |
rs46515923 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115377292 | AAACTACCTGAAAGA[G/T]ATCAATATGCCTAAA | 19016 |
rs46516710 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115464261 | CAAGTCCCATGCAGA[A/G]GACCTGGATCCAGCT | 19016 |
rs46527787 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115466424 | TCCTGCTCTTCTCCA[A/G]TCAATTTTAACATCA | 19016 |
rs46551961 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115482512 | ACACAGCAGAATAAG[A/G]GACAAGTGAAGGAGT | 19016 |
rs46557316 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115461206 | AAGCAAGGTCTCTTA[A/T]GAAGCCCCTGTAGGG | 19016 |
rs46559612 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115387426 | CACAACAGTATGTAA[A/C]GCTAAAACAAATTAC | 19016 |
rs46569499 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115456255 | AGAAGTGAACAGGCC[C/T]TTTCTGACACATGTG | 19016 |
rs46573145 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115374051 | TGCACGGCTTTTCCA[A/G]TGTTCTGGTCTGACC | 19016 |
rs46579198 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115451615 | ATGCTGGGTATATCT[A/G]ATGTTCAGAGTATAA | 19016 |
rs46591515 | snp | A/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420221 | TCACTCTGCCAAATG[A/T]TAGCATTTCAAATAC | 19016 |
rs46593553 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115445909 | AATGATAGGCCGGAT[A/G]ATTACTCTTTAGAAT | 19016 |
rs46616437 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115388769 | GGGGCCCCATTCTTA[C/G]AGTCAAACAAACAAC | 19016 |
rs46624428 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115383038 | ATTATTTAGACAATC[C/T]GCTCCCTGGACCTTC | 19016 |
rs46653552 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115410623 | ACACTGTTCCTGGAC[A/T]CTTCTGTTTTGGAAC | 19016 |
rs46667128 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Pparg | Mm_Celera | 6:115390955 | AATTCTGTTTACAAC[A/G]AGGATTCTTTTCTAG | 19016 |
rs46669448 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115380851 | AATGACAAGTGATGA[A/G]TCCAGTGTTCAGTGA | 19016 |
rs46692664 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115426601 | CCTGTAGCTAATCGA[C/T]AGACACAGGCATTGC | 19016 |
rs46706677 | snp | A/C | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115489765 | AGCTGCAGAGCCTCG[A/C]TCCACGAACCTGCTT | 19016 |
rs46707286 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115374334 | AATCAAGTCTGGAAT[A/C]GTGACTAAACACGGC | 19016 |
rs46755383 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115463846 | TAAGTTGCCTATGCT[A/G]CTCCAATGGAATGGT | 19016 |
rs46776012 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115472145 | AGGCCTGCTACAGCT[G/T]CATTTTCTGAAACAG | 19016 |
rs46804187 | snp | A/C | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115472314 | ATCTAATGCTGTAAG[A/C]TTAGTTTATGTTCAA | 19016 |
rs46807870 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115442285 | AGTGCTGTTCCTGTA[A/G]TCCAGCCACAGATCA | 19016 |
rs46810574 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115416494 | GGGAGTGGACCGTAA[C/G]TCTGCCTGTTTCTCG | 19016 |
rs46821177 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115489354 | AAGACTGATGAAAAG[C/T]CCCAGTAATCTCATC | 19016 |
rs46825452 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115363725 | GAAAAGGGCAAATTA[C/T]ACTTTAAAAAAAATC | 19016 |
rs46864347 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115401940 | AGGGCCTCAAACATG[A/C]TAATATAACACTCTG | 19016 |
rs46864888 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115424773 | TGCATACCACTTCTA[C/T]GGGGGATATTTAAAC | 19016 |
rs46882236 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115366602 | TTACTGTTTATAAAT[A/G]TTAGACATGTGTGGT | 19016 |
rs46888949 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Pparg | Mm_Celera | 6:115396402 | GTCAAACATTTCACA[C/T]GTAGCAGGCCAGCTC | 19016 |
rs46930217 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115372385 | TAAGAACAAGTATGT[A/G]CGTTTTCAGCATAAT | 19016 |
rs46931882 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115482692 | TGCATGAAGACAGGA[A/G]TTCAATTCCCAGACC | 19016 |
rs46946159 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115433052 | ACCATGGGACTCTGG[C/T]TACTCTCTCTATATT | 19016 |
rs46974811 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115476995 | AAGCTTAGCACTTCC[C/T]TAAAGGCAGCTCATA | 19016 |
rs46979254 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115437315 | GCAGTGACTCTGGCT[A/G]GGTCCATGAGGAGGG | 19016 |
rs46994829 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115458514 | AGAAATGCTAAATCT[A/G]CCTGTGGAACAAGTC | 19016 |
rs46995030 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115423991 | AAATTTGAGCTATTA[A/G]AGCCCAACAACCTGT | 19016 |
rs47014441 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115390728 | AGTAAGGACACATTT[A/G]TGGAAAACTTAGAAA | 19016 |
rs47026003 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Pparg | Mm_Celera | 6:115389528 | AATGAACAGGAAAAA[A/T]TAGATTATGGATGAA | 19016 |
rs47042077 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115373454 | AACGGGAAGGATAAC[A/G]AGCTCAAGGAGGTTT | 19016 |
rs47056713 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115380493 | AGAGATGGTTAGTGA[A/G]TATTCAATTATGTGA | 19016 |
rs47062784 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115461560 | GATAGAAATGTTCCT[A/G]TATACCTTGTCTTAT | 19016 |
rs47070578 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115373530 | ACTCTTTCATGTCTC[A/G]CTGCACACAGGGAAT | 19016 |
rs47078336 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Pparg | Mm_Celera | 6:115477513 | ACTCCAGGACACTCC[A/G]CGGGACACTTTGCCC | 19016 |
rs47085602 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115423057 | TTTTATAATAGAAGT[A/G]CAGAGCATTAAAATG | 19016 |
rs47088101 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115383450 | TCAAACAGCTATCTG[C/T]TTCTTTTATGCAACT | 19016 |
rs47089724 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115484685 | AGAAACCTAACCTGT[A/G]GCCTGCTGCTGTAAG | 19016 |
rs47101383 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115401715 | CATCTCTGATATTTT[A/C]AAATCTTACATGTCG | 19016 |
rs47102918 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115391084 | TTACAAATTAAAGCC[A/G]AGCACTTTTGTCTCC | 19016 |
rs47109359 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115446282 | GTGCTGCCGTGCTCA[C/T]CAGGAGAAGAGCTGA | 19016 |
rs47119864 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Pparg | Mm_Celera | 6:115473274 | ATTAGATGACAGTGA[C/T]TTGGCTATATTTATA | 19016 |
rs47133748 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115459468 | TACATGCAACATTTT[A/T]AAAAAAATAACCAGA | 19016 |
rs47137814 | snp | A/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115461923 | TTCTACCAAGTACTA[A/T]GATATATGTAAATGT | 19016 |
rs47144893 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115378799 | AAAAAAAAAGAGACA[A/G]CCTAACCTGCTAAAT | 19016 |
rs47150580 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115427282 | AAAAATATGCTCTCT[A/C]CTCTACTTCCCGGGA | 19016 |
rs47153077 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115426927 | TCTTCTAACAGTTGG[A/G]TGCCTGCTGCTTGCA | 19016 |
rs47166694 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115487049 | TTGGATCAGATGAGC[A/G]CAATCGGGGAAATAT | 19016 |
rs47177400 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115422365 | GAACCCTAATCTAAT[C/T]TCTATTTTATCTCTG | 19016 |
rs47182148 | snp | A/G | 0.42 | 0.183303 | intron-variant | Pparg | Mm_Celera | 6:115410593 | CTTTCTGCTACCATT[A/G]CTGCATACACCGTTA | 19016 |
rs47185637 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115400791 | GGATGTAGCAGTTGA[C/T]ACAGACACGCATGAC | 19016 |
rs47191338 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115448463 | AAAATATTGTCATGT[A/G]GAAAATTCCATGGGT | 19016 |
rs47192504 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115416772 | CCAATAAAATTGAAT[A/G]AAGCAACTTTTAAAT | 19016 |
rs47206358 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115471239 | AAAGAATGGAAACCT[C/T]CAATTTTGTCAGCTT | 19016 |
rs47212663 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115393526 | AAGACATGTATGCTA[C/T]AGATACTGTATAAAA | 19016 |
rs47213758 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115415101 | CAGGATGTTGCCTAA[G/T]AAATATCCATACGAC | 19016 |
rs47232520 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115449082 | TTACAAGTGTTTTAG[C/T]TAATGGACTATTAAG | 19016 |
rs47240515 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115411288 | TACCTGTGAGATCCA[A/G]CTAGTCTTTTACCTG | 19016 |
rs47270187 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115478725 | TCCGGCTGCTGATAC[A/G]GTGAATGCCAGTGTC | 19016 |
rs47272789 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420395 | AAACCAGGATCTGGG[A/G]ACAGGAATAAGGGAA | 19016 |
rs47277607 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115372387 | AGAACAAGTATGTGC[A/G]TTTTCAGCATAATTT | 19016 |
rs47297837 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115404116 | CCTCACTGAAAGTGT[G/T]GAGACCCATACTCCT | 19016 |
rs47299122 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115395679 | TGTGACTAACTGGTT[C/T]TGCATGATTTTAATC | 19016 |
rs47303097 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115453874 | GCATGAGTAACAGTA[C/T]CCACACAAAATGCCT | 19016 |
rs47311617 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115446062 | TAACTTACTGCTAAT[C/G]CCCAGCATTGGCACA | 19016 |
rs47322740 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Pparg | Mm_Celera | 6:115489011 | AAAAATTTAAATGCC[A/G]TCAATAAAATTTAAC | 19016 |
rs47326592 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115377998 | CCCCAGTCCTCAATA[A/G]CTCTCATAACTTTCT | 19016 |
rs47337936 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115386922 | ATAGTCACATTCCAG[A/G]AAAGGCTATGGTGCC | 19016 |
rs47358384 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115448952 | GTGAAGAGGAATATA[G/T]ATTTCATGTTTACAA | 19016 |
rs47359315 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115408806 | TTAGGTCTAGGTTGT[A/G]TGACATCAACTCCAT | 19016 |
rs47360866 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115372058 | ACCCCGACCACCAGC[C/T]TTTGAATTCAGAGTA | 19016 |
rs47396111 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115399611 | TCACAAGCCCACATG[C/T]GGGTCTGATTCACTG | 19016 |
rs47397400 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115388802 | TACCAACCAATAAAA[A/C/G]CAATAGTCTACTTTA | 19016 |
rs47400002 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115449987 | TAGCAGATTTTCTAA[A/G]GATTTCCCAATTGCT | 19016 |
rs47414705 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115388174 | CATTTTCTCTAGTCA[C/T]TGCCTGACTTTCCAT | 19016 |
rs47418265 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115382068 | TCTGGATAAGTTGCT[C/T]TTGGAATGCGTTAAT | 19016 |
rs47436013 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Pparg | Mm_Celera | 6:115430713 | TCTAGAGGCTGAGGC[C/T]AAGGTTACAACTTCT | 19016 |
rs47436850 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115447965 | GATCTGTTAGAAAGT[C/T]ACAAGTAAGCTGAGC | 19016 |
rs47442778 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115396283 | TCCAGGCCACTCCAG[C/T]GCCAAGCCAGCCTGT | 19016 |
rs47454032 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115382464 | AGCAGTTTCCCATAT[C/G]TTAAACATGCAAGAT | 19016 |
rs47469183 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115446015 | TTATGGCAATCAAAA[G/T]TTTTCACTAGCATGG | 19016 |
rs47478636 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115442750 | AGTTAGGACTTCTGG[A/G]CTCTAGATGGATGGC | 19016 |
rs47480311 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115403120 | CAGACTATACCAGGG[A/G]TCTTTCAAATGATGG | 19016 |
rs47487312 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115440917 | CTGAGCCACGGGCAA[A/G]CGCAGTACTTGCCTC | 19016 |
rs47493369 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115386043 | AAGTGCTAGAATATC[C/T]GCCTAGGAGGTGTGT | 19016 |
rs47507713 | snp | A/G | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115477289 | AGCCTGGAAGCCAGG[A/G]GAGCACTTCCTTGTA | 19016 |
rs47527350 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115378014 | CTCTCATAACTTTCT[C/T]GTGTAAAATTACTCA | 19016 |
rs47532972 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115393462 | GAGCTAACATGATAA[C/T]ACGATTAGAAAATTC | 19016 |
rs47583297 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115394500 | AACCCTCCAAGAAAG[A/G]TGTGAATACACAGTA | 19016 |
rs47594698 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115390856 | ACTGTTGACACCATA[A/G]CCTCCTACACACTGA | 19016 |
rs47606211 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115445555 | AAAATACACGTTGTT[C/T]TATAGACCCTAAAAA | 19016 |
rs47622601 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115396290 | CACTCCAGCGCCAAG[C/T]CAGCCTGTAGCTTCT | 19016 |
rs47635533 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115425036 | TAAAGCCCTCTGTGA[C/T]GCTTATTGTTTTAGT | 19016 |
rs47640716 | snp | A/C | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115425479 | TTGTGTTAAATATGG[A/C]AAAATTACTTCCCAC | 19016 |
rs47645327 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115392016 | AATATATCCCCAAAT[A/G]AACAGTCAGTCCATC | 19016 |
rs47645745 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115370121 | CAGTAAAGATCAAGG[A/C]AAAGCATGAGAGTCC | 19016 |
rs47654006 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115412003 | ACTCAAAATGAAACT[A/C]ATGTTTGTGGACATA | 19016 |
rs47662303 | snp | A/G | | | upstream-variant-2KB | Pparg | Mm_Celera | 6:115358945 | TTATAAAGAGACACT[A/G]TCACAAACAAACAGA | 19016 |
rs47676812 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115376150 | TCAAACTGTTTCTGT[C/T]AACACCTAGTAACTA | 19016 |
rs47685300 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115404149 | TGCACACCTTGGCTA[A/G]ACCATTTACCAGAAA | 19016 |
rs47689399 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115440910 | AATAGGTCTGAGCCA[C/T]GGGCAAACGCAGTAC | 19016 |
rs47710910 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115370203 | CTTAGTTTTGTTTAA[C/T]ATATTAGATTTACCT | 19016 |
rs47717880 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115453771 | GGAGGAATCTGCAGT[A/G]CACTTTAACCAACTC | 19016 |
rs47721052 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115389656 | TATGTGCATGCCTGT[C/T]CTTTGGTTCCTGCCA | 19016 |
rs47735522 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Pparg | Mm_Celera | 6:115484814 | TTCTCAAGGCAGAAT[C/G]AGATCTGGATAAGAT | 19016 |
rs47744145 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115377866 | ACATGTGCAGTTACA[C/T]AAGAGAGTCTGTCAT | 19016 |
rs47774491 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115385794 | GGTATGAGGCAGGTG[C/T]CTTCCCTTTCCCTAG | 19016 |
rs47779546 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115378346 | AAAAGAAGTCACTTA[A/G]CCATCTTGCTTAAGG | 19016 |
rs47784569 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115412101 | ATATGGTTGGAATGT[A/G]GTTTAATTAGTCCAC | 19016 |
rs47802509 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115437264 | AAGAGTAAGAACAGA[A/G]AGAGATGAAAATTAA | 19016 |
rs47822079 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115373148 | TTATGAACAACTTCA[A/G]AGTATTAGAATGAGA | 19016 |
rs47825383 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115489922 | GAGGTCTGACAAAGC[C/T]TCTTTTTGTCTTCTC | 19016 |
rs47825565 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115370728 | ATTTACACTTATATG[C/T]GTGCATACATGCAAA | 19016 |
rs47825605 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115381153 | ACAGGTCCTTGAGCA[C/T]ACTAGGCAAGTATTG | 19016 |
rs47829414 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115434520 | CCACAGAGCTTTAGA[C/T]CTTCTGCATTCAATA | 19016 |
rs47840030 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115473644 | GGCCAATCTGGTCTT[C/T]GGTTCATTTTAGTAA | 19016 |
rs47847398 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115372992 | TGCATCTGCCTCCTG[A/T]GTAAAGGGCTCAAAG | 19016 |
rs47852438 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115442224 | ACTACAAAAGGAAAA[A/G]CAAAGTTACGGGTTA | 19016 |
rs47852510 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115396066 | GTGTTTCCAAACATC[A/G]CTGTAATATCTTATA | 19016 |
rs47867862 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115424869 | AGAAGTTTAAAGGGA[C/T]GAAAATACAAGGACC | 19016 |
rs47884163 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115407188 | CAATGAGTTCAGGAG[C/T]ATGTGGTATCTGTAA | 19016 |
rs47892678 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115468384 | AAAAAAATCTAAGTA[C/T]CTGGAGAGGCCCATG | 19016 |
rs47898772 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115383212 | CTCTCATCAAACTGG[C/T]ATCAGACACCCTCCG | 19016 |
rs47916495 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | GRCm38.p3 | 6:115426984 | ACCTTTGCCTGGCTT[C/T]CACTGCCTTTTGGTA | 19016 |
rs47931858 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115425576 | TTTAAATGGAAGCAG[C/T]GATCGCTCATTTTCC | 19016 |
rs47960718 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115471898 | TGACAAATATGAATT[A/G]CCTTTCAAAGCAACC | 19016 |
rs47962382 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115388231 | ATTGTAGTGACCTTA[A/G]TGACATTACCTAATT | 19016 |
rs47965422 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115426405 | CTGAGAAATTTTCTT[C/T]ACTGACTTAGGGGAC | 19016 |
rs47968039 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115465660 | CAACAGAGGGCTTTT[C/T]ACTAGCCCAATATTT | 19016 |
rs47980264 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115386120 | AACTGCACACATCAG[G/T]ACCTCTCTGGGAACT | 19016 |
rs47980976 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115375658 | GATGCTGACCTTTAA[A/G]TCATTTGTTTTTTAC | 19016 |
rs47991782 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115402249 | TTAGAAGCTGCTCTT[C/T]TAAAGAATTGGGTCA | 19016 |
rs48005358 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Pparg | Mm_Celera | 6:115487480 | TGGGTCCTAAATGTT[A/G]TATATGAATCAATCC | 19016 |
rs48021862 | snp | A/G | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115451341 | TGCTTGATATCCTTA[A/G]TGGGAAGTTCAACAG | 19016 |
rs48030550 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115387994 | TCCTTTGTTCCTCTT[A/G]TCAGTTCCTTCTAAA | 19016 |
rs48033604 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115399551 | GCTCTTCAAATGCAT[A/T]CCTTGGTGCAGTGGG | 19016 |
rs48034996 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115454238 | GATTCCACAGTGACC[A/G]TCAAAGGAAACAAGG | 19016 |
rs48036671 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115413899 | TTTATTAACCAAGAA[A/T]CAAACATAGGGATCA | 19016 |
rs48040639 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115453827 | AAAATTTTCTACATG[A/G]CTGTGGTTATACTAG | 19016 |
rs48044189 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115489853 | CGAGAACTGGGTTTC[A/T]TCTCCAGCCTGGGGA | 19016 |
rs48061510 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115431966 | ATACCCACAATTTTT[A/C]CAAATAAATAAATAG | 19016 |
rs48074969 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115489795 | TAAGAAACAGGGCGG[C/T]GATGGGGTCTTGGCT | 19016 |
rs48090518 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115430549 | TGGGAAAGGATATGA[A/G]TCTGAGGGTCAGGAA | 19016 |
rs48092597 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115418752 | GTGCACTCACTGAGG[C/T]TAAAAGCTGTGGCTT | 19016 |
rs48102789 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115427405 | CACTATTCTCCATTC[A/G]CCTCTTATCCATTGT | 19016 |
rs48103034 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115407387 | GTCTAGTCTTTGAAA[A/G]GTGTAACCAAACATC | 19016 |
rs48114725 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115462764 | CTTGAAAGCTCTATA[A/G]AGATGACTTTGCATC | 19016 |
rs48114726 | snp | C/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115459598 | TTCTGCCTCACTATA[C/T]GATAGCTCTGGTTTT | 19016 |
rs48119852 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115418427 | TCTCCACTGAGAACT[G/T]CAAAATTCTGATAAC | 19016 |
rs48138334 | snp | A/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115410831 | AATTTAGTTATGATA[A/T]TATGCAGATAATCTA | 19016 |
rs48162222 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115387070 | AATGAGTTGCTTGTA[A/G]GTTAATTTACAACTA | 19016 |
rs48214315 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115473521 | TCCCAGGTTCCTCGA[A/G]TTTGTTCATCACACT | 19016 |
rs48214709 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115443547 | GCAAGTTCTGAGACT[A/C]AAAAGTTTGATTCCC | 19016 |
rs48217079 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115374910 | ACAGAGCTATAATAG[C/T]AAGCAAGGCAGAGCT | 19016 |
rs48234081 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115397775 | TTTGCGGGGATGAAC[G/T]CACTCTGGGACCATT | 19016 |
rs48234912 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115390731 | AAGGACACATTTGTG[A/G]AAAACTTAGAAACTA | 19016 |
rs48237601 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115395076 | GATGCTTCTGGATTT[A/G]TTGAAACTTAAGTGA | 19016 |
rs48246573 | snp | C/G | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115477214 | TGATACAGGATCACC[C/G]TTCACTCTCAGCAGC | 19016 |
rs48252542 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115388662 | ACACAAGTGATTTTG[C/T]TGTTCTTATTGTTTT | 19016 |
rs48257640 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Pparg | Mm_Celera | 6:115462342 | CATTCACACTTCCTC[A/G]CTCCTTGAGAAGCCA | 19016 |
rs48274129 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115405000 | TGAATTTCTCAAGAT[G/T]AAATAGATACTATAT | 19016 |
rs48297118 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115442261 | TCTGTCCCTACCAAG[C/T]CCTAATCTAGTGCTG | 19016 |
rs48297967 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Pparg | Mm_Celera | 6:115386110 | AACAGATCCCAACTG[C/G]ACACATCAGTACCTC | 19016 |
rs48307662 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115430566 | CTGAGGGTCAGGAAG[A/C]AAAAGAGATGGTCAG | 19016 |
rs48309471 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115419971 | GACATGGGAAAGAAG[A/C/G]TATTGCTAGACCAGC | 19016 |
rs48317553 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115398744 | GCTGCACAGAAGCCT[A/G]GGCAGGGCAAATCTT | 19016 |
rs48325396 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115411138 | TCATTCTACTTCTAC[C/T]GCCTTGTCTGTGTCA | 19016 |
rs48343950 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115465379 | CTAGAAATCACTTGG[A/G]AACCTCATCCCAGCT | 19016 |
rs48350439 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115382031 | TCAATTTTCACTGTT[C/T]GTTCCATTTCAGGCA | 19016 |
rs48361301 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115368640 | GAAAGTGTATCCATA[G/T]GCATGTTTTTCTTGT | 19016 |
rs48373822 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115365041 | CTTTGTTTCTATTTG[C/T]TTGTCTTGGGTATGG | 19016 |
rs48380975 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115432916 | TCCTTTTCCAGAGGT[C/T]TTTAAAACAGGACAT | 19016 |
rs48386723 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115364117 | TGTAGGTGCCCGGTG[C/G]GTATGGCAAGACATG | 19016 |
rs48387096 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115415490 | TATTCTATTATTCTA[C/T]CATGTACCTTAGCAT | 19016 |
rs48395076 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115449955 | TAGTCCCAGAAGGAC[A/G]TATTTGCATTTTGAG | 19016 |
rs48402938 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115419563 | TAGGGCAAAAGAAGG[A/G]CGTTAAAACACAATC | 19016 |
rs48422242 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115416172 | ATGTAGCTTTGTTGT[A/G]TTAATTGCCTTAGAA | 19016 |
rs48442080 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115396743 | TTTCAGCCTGGACTA[C/T]CACATTATTTTAGAA | 19016 |
rs48451778 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115374405 | CAGCACCAGAGAATG[A/G]ACAGTCAGAAACAGG | 19016 |
rs48456298 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420749 | CCAACACAGTGATCC[C/T]CCATCATTTGGACTA | 19016 |
rs48482098 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Pparg | Mm_Celera | 6:115373683 | AAACAACAACCCATC[A/G]CAACATGGTGATTCA | 19016 |
rs48502972 | snp | A/C | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Pparg | Mm_Celera | 6:115463669 | GTGTCCCACTTCTAC[A/C]TTTCAGTTTTTCTAT | 19016 |
rs48503631 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115396062 | CCGAGTGTTTCCAAA[C/T]ATCACTGTAATATCT | 19016 |
rs48506771 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115407109 | GATTTATGTATACTC[C/T]GAATATCACAGGAGA | 19016 |
rs48534528 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115364799 | AGGCCATACTTTGGC[A/G]AAATGTACGGTTCAT | 19016 |
rs48537902 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115380872 | TGTTCAGTGAAGTTG[C/T]TGTTTATGATGTTAT | 19016 |
rs48538278 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Pparg | Mm_Celera | 6:115411243 | CTGGAATTTCTTGGA[C/T]ATGTGAAAAGTTCAT | 19016 |
rs48542217 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115472164 | TTTCTGAAACAGATG[A/G]CTTCCAGAGCACAGA | 19016 |
rs48550544 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115467510 | TCTGAACTAATATTA[A/T]TCTAGGTTTGGATGT | 19016 |
rs48551179 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115467195 | AAAATATACAGTGGC[C/T]GTCACATCATACTAA | 19016 |
rs48551399 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115418741 | TGAAATTAAATGTGC[A/G]CTCACTGAGGCTAAA | 19016 |
rs48560795 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115478916 | AGGAAAGTTATAAAT[A/G]CAGGCTGGGGGATTG | 19016 |
rs48568327 | snp | G/T | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115412677 | GTCAGAATTAGGAAA[G/T]CTTCGTGTTATAAAC | 19016 |
rs48569935 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115414097 | GCACTGAAATGCAAA[A/C]CCCGATCTCCTGCAC | 19016 |
rs48599572 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115435722 | AAGGCTGCTCATTAA[C/G]CATAACAAAAATGAA | 19016 |
rs48603004 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115477597 | TCTCCAACAGGAAAA[A/G]GCTCTTGTTAATTCA | 19016 |
rs48617239 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115401799 | TAGAGTCTTATAATA[G/T]GAAGAATATGTATGC | 19016 |
rs48656617 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Pparg | Mm_Celera | 6:115391157 | TTTCTTTCATAATGA[C/T]AGTAAACTTGCAGTA | 19016 |
rs48662130 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115427078 | CTCTCTTCAGACTAA[C/T]CTCACTTTGCAAAAA | 19016 |
rs48666115 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115465091 | GGCTCTGGGTTCTTA[C/T]TGTCATAACCTCAAG | 19016 |
rs48673253 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Pparg | Mm_Celera | 6:115487204 | GCAGCTGGAGTCACT[A/G]TGAAGTGAAGAGGCT | 19016 |
rs48677866 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115395808 | GTTGTAGTAACTTAA[A/C]CGTTAATTTGATTCT | 19016 |
rs48680491 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Pparg | Mm_Celera | 6:115408425 | GTATCAGAACCCAAA[A/C]TAAAGAACTTGTTAT | 19016 |
rs48692807 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115398614 | AATAGACTTTAGCTC[A/G]CAGCCCTAAAGACTT | 19016 |
rs48729131 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115398932 | TTTTAGGGAGGAACA[A/G]GCCATATCTAACTAC | 19016 |
rs48748101 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115386072 | GTGTGCTACTCAGCA[C/T]CCGTAGCTGGGGGTA | 19016 |
rs48748851 | snp | A/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Pparg | Mm_Celera | 6:115463508 | TCTGAAAAGGGAGTA[A/T]GTCCTCCAAGCTGTA | 19016 |
rs48749550 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115394740 | AATTAGGTAACAGGA[C/T]CATAGCTGTGCTTAG | 19016 |
rs48751404 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115414031 | AATTCTTTAGATGAG[A/G]GAACAAAGGTTTAAC | 19016 |
rs48760246 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115453956 | GGAGCTGTTTCAGTA[A/T]ATACAAGAATGAACA | 19016 |
rs48762117 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Pparg | Mm_Celera | 6:115373691 | ACCCATCACAACATG[A/G]TGATTCAAGGCTGAA | 19016 |
rs48764611 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115436602 | ATAGAGAACACAAAA[A/G]CCATGCAGAAGAACT | 19016 |
rs48771727 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115385539 | TAAGTTAAATAATTT[C/T]CCAGCTATAAAATGT | 19016 |
rs48772528 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115422709 | TACTCCAAGCATAAT[A/G]TCTGATTGAAGAATA | 19016 |
rs48785507 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Pparg | Mm_Celera | 6:115469058 | TTCTCATCATTTGCA[G/T]ATTTTTCTTAGACAT | 19016 |
rs48792911 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115484915 | AAAGAGCCCTTCCCA[A/C]TTTGCAGCCTGGGGA | 19016 |
rs48797977 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115440935 | CAGTACTTGCCTCAC[A/T]CAGGTTGCTCCCACT | 19016 |
rs48819222 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115381163 | GAGCATACTAGGCAA[A/G]TATTGTACCACTAAG | 19016 |
rs48823568 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115379039 | AGTGTGTGGCAGTGA[C/T]TTAAAAATACAGTGT | 19016 |
rs48840924 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115371607 | TGTGGAATATTGAGG[A/G]AACATCAATTTAGGC | 19016 |
rs48857463 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115476863 | GTTTAGCAACTCCTC[C/G]TGAACTCAGCTCTTG | 19016 |
rs48879111 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115379009 | GGCTAGTTGTTCTTC[A/G]TGGTAAATCAATTTA | 19016 |
rs48889230 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115395106 | AAAATACAACAGCTG[A/G]TAGAAAGGCCCAGAG | 19016 |
rs48892090 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115400499 | GACTTAAAAGGAAAG[A/G]AGTCAATTGAAGCTT | 19016 |
rs48896778 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115442271 | CCAAGCCCTAATCTA[A/G]TGCTGTTCCTGTAGT | 19016 |
rs48897794 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115454259 | GGAAACAAGGGCCCT[A/G]GAGAATAATGCCAAA | 19016 |
rs48901837 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115440477 | TTCAGTAAGTCATAG[C/T]TGTAGGTCAACTTAC | 19016 |
rs48904338 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115392066 | GCAGAGCCACCTTCT[A/G]TGCTTCTCTAAAACT | 19016 |
rs48904447 | snp | C/T | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115488855 | TGTAACACTCCCAAC[C/T]ACATCACCCACAGAT | 19016 |
rs48932424 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115404893 | GTTGGGTTAAATATC[C/T]TTTTAATACAGATTT | 19016 |
rs48933835 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115388091 | TTTCTCCCATAGTTT[C/T]CCTAGTTCTTATAAG | 19016 |
rs48934335 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115410780 | GTAATACTGGGTACT[A/G]GAGAGTTTATAATCT | 19016 |
rs48945274 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115457677 | AGTAACACAGAGAAT[A/G]TTTTCCTTTTGACAT | 19016 |
rs48969467 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115464783 | CACGAGTCACAGTAC[A/C]ATGGGCTCTGTGCAC | 19016 |
rs48978814 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115396414 | ACATGTAGCAGGCCA[A/G]CTCCAGCCATCTGGT | 19016 |
rs48986928 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115446538 | ATATCACAGTGAATT[C/T]AGAAAAGTCTCACTA | 19016 |
rs48992062 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115452895 | TTTAATGCTATTTGG[A/G]TTTTGCCTATTCAAA | 19016 |
rs48999177 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115396775 | AGTGGCCAATTTGCT[A/G]TGATATATACATAGA | 19016 |
rs49001185 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115384176 | CTAACATGGAGTATG[A/G]CTTCAGGGTCCATGA | 19016 |
rs49005900 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Pparg | Mm_Celera | 6:115381274 | ATTTTTTTCTAATGC[C/T]TTATATGTATTTATC | 19016 |
rs49010268 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115436124 | TATGAAGTGATGCTG[C/T]TGAGGTCAAGGTGTC | 19016 |
rs49020640 | snp | C/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115403965 | TCATAACTATAATTC[C/G]CAACCACAGGTGGAG | 19016 |
rs49057437 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115413347 | GTCTAAACAGGAGTG[C/T]GTATCGTAGGACAGC | 19016 |
rs49080845 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115370351 | AGATGGCCTATGATC[G/T]TTTTGATCTTTAGTT | 19016 |
rs49082243 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pparg | Mm_Celera | 6:115390575 | ACTGACCTCTAGAAC[C/T]TACTATATAATTCCA | 19016 |
rs49083405 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115456418 | TGCTCTTTCTCTAGG[A/G]GCCCTGCCTCTTCTC | 19016 |
rs49097663 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115426653 | CAGCCCCACTCATAC[A/C]ACCTCAGAACTGAGG | 19016 |
rs49098305 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115403239 | TGGAGTGTCTATCCT[C/T]CATGACTACATTGTG | 19016 |
rs49113506 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115386493 | GCAAATATGCAGTTT[G/T]GCATCAGAAGGAGTG | 19016 |
rs49139324 | snp | A/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115373170 | AGAATGAGAAACTGA[A/T]TTGCATATAAAAGCA | 19016 |
rs49153269 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420733 | TAGAGATAAAACTAA[C/T]CCAACACAGTGATCC | 19016 |
rs49155581 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115372714 | GTCGACTCTCAACAG[C/T]AACTGTGACAAATCC | 19016 |
rs49158145 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pparg | Mm_Celera | 6:115462222 | AATTTTTTTGGGGAA[A/G]GCCTTGCACATGCCA | 19016 |
rs49165491 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115422511 | TTTCAGAACACTTGG[C/T]GAATTAGCTTCCTCT | 19016 |
rs49172694 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115394484 | GGGCTTGTTAACCAC[A/G]AACCCTCCAAGAAAG | 19016 |
rs49185728 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Pparg | Mm_Celera | 6:115455298 | GGCATCTTTTGCATC[A/G]CACAATCAATGTGAT | 19016 |
rs49187053 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115374562 | ACCTGGCAGCTGCGT[A/G]CAGAGAAAGCCACCA | 19016 |
rs49211668 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115398989 | TATTGGTTTATGCCA[C/T]TTGCCTTGAACTTGC | 19016 |
rs49229312 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115414186 | CTAGACCCTCACACA[C/T]GCTAGGCAAGTTCTC | 19016 |
rs49246176 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Pparg | Mm_Celera | 6:115483978 | AGCCGTCCTACATGT[A/G]TGTTTTCAACTGTGA | 19016 |
rs49270096 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115383329 | AAAATCTAGGTTTTC[A/C]TAAGTCTGAATACTG | 19016 |
rs49270620 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115422943 | CACAGCTTCTTCTAT[A/T]TTGTATCATTTCTTA | 19016 |
rs49318708 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115416108 | TGGACTCAAGTTAAT[A/G]TCATTTCACTGAGTT | 19016 |
rs49326250 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115410919 | GGTGGTTCAGTGCTT[A/G]CTTAGAATTCATGAG | 19016 |
rs49326734 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115471890 | GAGTGTCATGACAAA[C/T]ATGAATTACCTTTCA | 19016 |
rs49361626 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115428431 | CTTCTTTCTGAACTC[C/T]AAGGGCACCTGACAC | 19016 |
rs49388145 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115394071 | GTTGTTGCAAATATT[A/G]AAAATAAGTCCACAA | 19016 |
rs49388417 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115432994 | TCTTCCTCTTCCTGT[A/C]CCCCAGAGGCCGCAT | 19016 |
rs49388585 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115449857 | ACACACACATATATA[C/T]ACACTGGAGCTAGAA | 19016 |
rs49422337 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115470861 | CAGCAAGCCTCTGAG[C/T]CCTCTAGTCTCTCCT | 19016 |
rs49424324 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115426503 | AATACTTCCTGAGTA[C/T]TTGTGTTGGAGTCAT | 19016 |
rs49439347 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115369272 | CTATGTGAAGTTCCT[A/G]GCCATATTGCACCTT | 19016 |
rs49443131 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115402458 | GAAGGCCTGAGCTCC[A/G]AGCCAGCCTCCTGGA | 19016 |
rs49457252 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115464987 | GGTGCAGGAAAGAGG[A/G]CTGGAGTCTGGGATC | 19016 |
rs49464731 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115463031 | TAGGGAGAGCACAAT[A/G]CGGAGCCCTAGTAAT | 19016 |
rs49467435 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115380651 | ACATCATCTTTGGAA[C/G]TTGAAATCCTTGTCT | 19016 |
rs49472107 | snp | A/G | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115414337 | TTCTGTGCAGCTCTA[A/G]GATACTTTTTTTTAA | 19016 |
rs49484448 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Pparg | Mm_Celera | 6:115408656 | TCGTGGGATTTAACC[A/G]TCACAATAAGCAATC | 19016 |
rs49502144 | snp | C/T | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115365552 | CAGCTCCATAGTTTA[C/T]TACCAACACCTAAAA | 19016 |
rs49521412 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115482547 | CCTGAGCTAAAGCTC[A/G]GAAACCTGCTACATG | 19016 |
rs49537399 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115383616 | GCATTTTGGCAGATT[G/T]GAATGTCTGAGAATT | 19016 |
rs49546716 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Pparg | Mm_Celera | 6:115397676 | GAGATCAGAATGTTC[A/C]GACTTGTAGTTTTGA | 19016 |
rs49558530 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115419100 | ATATGCCACCAGATA[A/T]GTAAGCAACATTTAT | 19016 |
rs49578823 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115397472 | CCCAGATCAAAGTTG[A/G]AACCAGTGTCCTTTC | 19016 |
rs49583317 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115398828 | GCCACAGTCACTTCT[A/G]AAGCTGTATGCCACC | 19016 |
rs49590819 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115487010 | GCTGGCAACACAAGG[A/G]AAGGAGGACTTAAGT | 19016 |
rs49597395 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115395176 | AAAGTCAGACGTAGA[C/T]GTATCAGTTTGCATG | 19016 |
rs49602174 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115405887 | AAGGAGCCTCGTTAG[C/T]GCAGTAGGTAGCACT | 19016 |
rs49603777 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115400122 | TGGAGACAGAAGGCC[C/G]GAGCTCAGAGCCTGC | 19016 |
rs49604417 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115436968 | ATTGAACCCCTGTTT[C/T]AAAAACCTTAGGTGT | 19016 |
rs49607467 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115382723 | GATGGGGGATACCAA[C/T]AAGCAAAGCTCCCTG | 19016 |
rs49608106 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115386936 | GGAAAGGCTATGGTG[C/T]CTTTTACTCTTGGGA | 19016 |
rs49639358 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115388836 | CAAAGACTGTTTCCT[A/G]TGGCTGTACAAACTT | 19016 |
rs49671876 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115468116 | TTCTTCCTATTTAGA[A/G]AGCAATGATGTGTGC | 19016 |
rs49675580 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115375633 | AGTGAGTTACGTAAA[C/T]CTAAGTCAAGATGCT | 19016 |
rs49676025 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Pparg | Mm_Celera | 6:115468341 | TTTGAAAGATAGGCC[A/C]TAAGAATGTAGTGTT | 19016 |
rs49683776 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115467999 | AGAGTTTAAAGCCAT[A/G]GAGAAAGAATTTGAA | 19016 |
rs49687066 | snp | A/C | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115364778 | TAAGGAGATCTCAAA[A/C]ACAATAGGCCATACT | 19016 |
rs49687151 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115449567 | TGTGTATGATATTTG[A/G]ATATGGGCGTACACA | 19016 |
rs49695232 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115424729 | GCCCTTTGAAACCAG[A/T]GTCCCTCAGAGATGG | 19016 |
rs49697640 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115400389 | AGTGATTTTTATACA[C/G]TGACAAATTGATATG | 19016 |
rs49704236 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115444818 | AGGGTAGCTCAGGAA[C/T]GCAGCTCCTATTTGC | 19016 |
rs49709053 | snp | A/G | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115460271 | TTCTGTGTGAAAGAG[A/G]TGGTGGTTAGCCATG | 19016 |
rs49709124 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115370499 | CTAAAATGGAGTGAC[C/T]TCATGTAAGAGTTAT | 19016 |
rs49709973 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115466513 | GGTATTCTAGTCTCA[A/G]GGTTAGGAGGAGGTG | 19016 |
rs49713663 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115471020 | GGTGAAAATCAGGGA[C/T]GCTTATCTGCAAGAG | 19016 |
rs49718138 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115370621 | AATGAGACCTTGGTG[C/T]GAAATATGGTAGAAA | 19016 |
rs49720645 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115443696 | ATCATCAGTACCCAT[A/G]AGAACTAAGGAGAAT | 19016 |
rs49723006 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115391050 | GATGCATTCTTATTC[C/T]TGAGTCTCTCCTTAA | 19016 |
rs49750521 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115436465 | CTTAATCTTTTTAGG[A/G]GAGCTTACATCTTGA | 19016 |
rs49751526 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115445546 | AGCAGATGGAAAATA[C/T]ACGTTGTTCTATAGA | 19016 |
rs49758928 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115472756 | GTGCCTTCATCTTTC[A/G]CAGTTTTCCTCAGCA | 19016 |
rs49766924 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115403178 | ATATGTTTATATATT[C/T]GAGCACATGTGAATA | 19016 |
rs49783951 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115385784 | TCAGATCAGAGGTAT[A/G]AGGCAGGTGCCTTCC | 19016 |
rs49789653 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115444833 | CGCAGCTCCTATTTG[C/T]TGAACTGAGGCTGCA | 19016 |
rs49809031 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115443603 | TAGAGCCTGAAGAAA[C/T]ACAACTTAAGCACCA | 19016 |
rs49810194 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115393616 | CTTGAGTCTGTCATC[C/T]AAGATATCTCAGCAT | 19016 |
rs49813304 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115395141 | ACATATGTGAGGGTA[C/T]ATGACTGACCTTCAT | 19016 |
rs49813623 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Pparg | Mm_Celera | 6:115488650 | ACTTTGTATGTTATA[A/G]AAAGCCTAGGTGCAT | 19016 |
rs49817467 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Pparg | Mm_Celera | 6:115436883 | AGTAGACCAGTAGGA[A/T]ATGCCAGGCATGGAA | 19016 |
rs49819416 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115470788 | AGGGTAAACCAAAGC[G/T]AGATGTCCAAGAAAC | 19016 |
rs49839089 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115489456 | TGGTAATGGGATGTG[C/T]TTGTGCTAAGCAAAA | 19016 |
rs49851616 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115388345 | TATATATCATATATG[A/T]TCTGGCACCTATTTA | 19016 |
rs49851878 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115373126 | ATTTTCCAAGAAAGA[C/T]CTGTATTTATGAACA | 19016 |
rs49862737 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115375726 | GTGATTACCCATTTG[A/G]AGATAACTTTAGGGT | 19016 |
rs49870053 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115449376 | CCTATTTGTTTAGTA[C/T]TCAAGACATTATCCT | 19016 |
rs49878987 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115397199 | ACTCAGTTTAGTACC[A/G]AGTAGCCTCAGAGGT | 19016 |
rs49881521 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115474594 | CTGGGAGCCAGCCAT[A/G]ATGGTACACAGCTAT | 19016 |
rs49889081 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115431165 | ATGTATCATATACAC[C/T]AAAGTACATGCATGA | 19016 |
rs49933634 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115424835 | CAGTCAGATACTTGA[C/T]TAAAATTCTCACCTG | 19016 |
rs49953745 | snp | C/T | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115454974 | AGTCACACTTGAACA[C/T]GTGGGAGACAGTGTA | 19016 |
rs49956889 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Pparg | Mm_Celera | 6:115371779 | CACATGAATGGTGAA[G/T]CTGGGGCTTAGGAGG | 19016 |
rs49961670 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115402091 | TTTATTTTGGTAAAT[G/T]TTATAGGACAAATTA | 19016 |
rs49977914 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115424038 | GTTTTGTGGTTGACC[A/G]TTAAATATTTATTCC | 19016 |
rs50023090 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420670 | GTAGTGACGTTTCTA[A/G]GCATTGAGAAGAAAA | 19016 |
rs50033480 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Pparg | Mm_Celera | 6:115372232 | TGTCATGTATTATTA[A/G]AGTATAGGGATGTGT | 19016 |
rs50042774 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115423438 | AAAGTGGTCGCTATT[C/T]ATATTAGTTTTATTT | 19016 |
rs50061509 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115440202 | CGCTTGAAGTTCTAG[A/G]TGTCTGTGGGAGGCC | 19016 |
rs50062311 | snp | A/G | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115451784 | CAAAACTTCAATGCT[A/G]CATCAATGCAAGGGG | 19016 |
rs50066315 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115373281 | AGATGTTGAATGAAG[A/G]TAGGAGTCTGTTTGC | 19016 |
rs50100600 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115416509 | GTCTGCCTGTTTCTC[A/G]GAGGCCTCACCATGA | 19016 |
rs50103205 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115411207 | TTTTATCAAAAAGGA[A/G]GTCAGAGTGAGTATA | 19016 |
rs50104455 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115426681 | AGGCCTCACAGTGTT[C/T]GAACACCAGTGCTTT | 19016 |
rs50104850 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115450887 | TTTATCCACAGGTTG[C/T]TGCTTCTATGTATCA | 19016 |
rs50109068 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115372830 | GATTCCCTTTCATAC[A/G]TTTTGCCAGGTTAGA | 19016 |
rs50109873 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115418185 | CTTTCTTGAATAATT[C/T]GTTACCTACTTTCTT | 19016 |
rs50121041 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115409714 | ATTTAGAAAATGAAC[A/G]TTTCACAACTCAATT | 19016 |
rs50122363 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115446521 | TATGCTTGCACTAAT[A/C]AATATCACAGTGAAT | 19016 |
rs50122982 | snp | A/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115395706 | AATCGAGTTTTTCAC[A/T]TGGCTGCTATGTTAA | 19016 |
rs50129312 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Pparg | Mm_Celera | 6:115478887 | CAGGTCATAAGAGAT[A/G]TAAATGGTTACAAAG | 19016 |
rs50130719 | snp | A/C | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115424794 | ATATTTAAACTGTCT[A/C]AGGGGCTCTAGCTAA | 19016 |
rs50142915 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115377042 | GGGTTTGACAACTAC[C/T]TCTCTTCTGAAGATT | 19016 |
rs50159425 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115411089 | TCCATGCACAGCCTA[C/T]TAGAGGTTGATGTAT | 19016 |
rs50166780 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115412177 | ATTCTAGATAACTTT[A/G]GAAGCACCAGTTGAA | 19016 |
rs50255178 | snp | A/G | 0.5 | 0 | intron-variant | Pparg | Mm_Celera | 6:115413404 | ATAATACAGCATCTG[A/G]ATTCTAGAGATACTT | 19016 |
rs50259438 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Pparg | Mm_Celera | 6:115366038 | TGCAAGGTTGGGCCT[A/G]TGGAGGCAACGGAAG | 19016 |
rs50268590 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115422544 | TATTGTGTTAGATAT[A/C]TTTCATTACAGTTTT | 19016 |
rs50279659 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115464434 | CAGGTTATTTCTTTC[G/T]TTTTAGATAAATGAC | 19016 |
rs50305684 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115408815 | GGTTGTGTGACATCA[A/C]CTCCATTCAGTGAGT | 19016 |
rs50311459 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115399049 | GTACTTAACAGGCAT[A/G]ATTGGCTTATGGTTT | 19016 |
rs50345133 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115481854 | AACTCAGAAGACCCA[C/T]TTCCATCCTCAAAGA | 19016 |
rs50353476 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pparg | Mm_Celera | 6:115453658 | AAGCAGCTCAACCAT[G/T]AAAGGACTTACAGAT | 19016 |
rs50368694 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115375100 | CATTAGAGCCCAAAA[A/G]AGTCTTTAAGATGGC | 19016 |
rs50378800 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115368401 | TGTTAGAAACCGAAG[C/T]TTGATGGCCTTACTA | 19016 |
rs50392251 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115394424 | TGGTAAAATCCATAG[A/G]AGAAAGCATGCGTGC | 19016 |
rs50394197 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115374813 | CCTCAAATTAGGGCA[C/T]ACTGTCTTGAAGAAA | 19016 |
rs50398626 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Pparg | Mm_Celera | 6:115406199 | CTTTGTGGTTAATGT[A/G]TCTCCTGTTTTGGAA | 19016 |
rs50403132 | snp | A/T | 0.375 | 0.216506 | intron-variant | Pparg | Mm_Celera | 6:115406930 | ATTTTCAGTAAAATA[A/T]AGCCATAGGAGATGT | 19016 |
rs50430462 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115462371 | CAAATTAAAGGTATT[C/G]TGATGAACCTCATTA | 19016 |
rs50433963 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115467097 | ATAGTATATGAAATA[C/T]AAAACCTCTGAATCA | 19016 |
rs50437409 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115460042 | GAAAGCCTAGCATTT[A/G]GAAAGCTTTTTCAAA | 19016 |
rs50438447 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115372094 | ACTGTTCTTAATCTC[C/T]GCCTAAAGGACAGAA | 19016 |
rs50439565 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115377799 | TAACTTCTTTTTCCA[A/C]ATAGCATCTGTGCTG | 19016 |
rs50449363 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115374321 | TCCAGTGTAAGAAAA[C/T]CAAGTCTGGAATCGT | 19016 |
rs50460108 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Pparg | Mm_Celera | 6:115460373 | ATCGGCATAACTGGC[A/G]TTTCCATGTCATATT | 19016 |
rs50461332 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Pparg | Mm_Celera | 6:115456200 | GAAGGAGATGTGAGG[C/T]TCTGTCCCTGTTCAG | 19016 |
rs50472484 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Pparg | Mm_Celera | 6:115408586 | TCTTACAGACATTTT[A/G]AGACAAGTTTGAGTA | 19016 |
rs50473175 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115486814 | AGTCTTCACTGTGGT[A/G]ATTCTACCTTCAGGC | 19016 |
rs50487895 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115425437 | CAGCCGCTGAGCTTC[A/C]TCTCCAGCCTTGGTT | 19016 |
rs50492312 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115369442 | GACAGGGTCTCACTG[C/G]TTCTTTTTGTCTTTG | 19016 |
rs50492989 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115443749 | CTTACCTGTACAAAG[C/T]TTAAAATGCACCTTG | 19016 |
rs50509784 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115472213 | TTTCTTGGCTCAATA[C/T]TTTTAATCTGCTTTG | 19016 |
rs50510110 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115381053 | AAATGCACTGTCATA[C/T]TTCACAATTAGGACC | 19016 |
rs50521822 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115388830 | TTATAGCAAAGACTG[C/T]TTCCTGTGGCTGTAC | 19016 |
rs50528679 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115404211 | GTCTCTCCCACCCTC[A/G]CCATACTTTACTTCT | 19016 |
rs50530491 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115421117 | AAGGGCTGCTCCCAC[A/G]TTAGCAGTTTGGCAC | 19016 |
rs50581552 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115373433 | TTGCTTCCTGAGAAA[A/G]AGCACAACGGGAAGG | 19016 |
rs50608664 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115384386 | CCTGCAAATGCATTT[A/T]AAAAAACCTGTAAGA | 19016 |
rs50612589 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115386579 | ACCTGAATTTTTCTT[C/T]TCTTAACTTGCTTGC | 19016 |
rs50635040 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115438134 | AATGTTGAATTGACA[C/T]AGCTCTGTAGCATTT | 19016 |
rs50662719 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115386740 | GGCAAGAAAGTAAAC[C/T]GGGAACAATTGGCAT | 19016 |
rs50663430 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115466994 | ACTTTGGGTTCCAAG[A/G]CATCATGTTGTTTAA | 19016 |
rs50665069 | snp | A/C/T | 0.35503 | 0.226867 | intron-variant | Pparg | Mm_Celera | 6:115409942 | ATTTTGATTGGTTCG[A/C/T]GACTGCCTATAAATC | 19016 |
rs50666998 | snp | A/T | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115364523 | AGTTGACCAAAAAAA[A/T]AGCAAGGCCAGTTAA | 19016 |
rs50673506 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115453672 | TGAAAGGACTTACAG[A/G]TGACTAACAAAACTT | 19016 |
rs50695884 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115376771 | GTACAAAGTGAATAG[C/T]TTAACCTGAACATTC | 19016 |
rs50698365 | snp | G/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115363123 | CAACCACATTTGCTC[G/T]AAAGTAAATGTCCGA | 19016 |
rs50700496 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115441117 | TTTCAATAAAACCCA[C/T]AATAGCAGAATGGAT | 19016 |
rs50712508 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115482497 | CCAGGAAAACCAGGG[A/G]CACAGCAGAATAAGG | 19016 |
rs50723641 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115470985 | GTCTAAGAGTCCTCA[A/G]TGTGGAACAGACTGA | 19016 |
rs50725392 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115461260 | TATAGGGCCAACTGA[A/G]ATGAACTTACACATT | 19016 |
rs50735562 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Pparg | Mm_Celera | 6:115483924 | CTACAAGACATATGT[C/T]CCTGGACACATGGCT | 19016 |
rs50749267 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115393464 | GCTAACATGATAATA[C/T]GATTAGAAAATTCCA | 19016 |
rs50795992 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115457872 | TTCTCTGCTTAAAGG[A/G]TAGGAACTGGGCTGG | 19016 |
rs50803857 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115402144 | GCTCCAAATTGATGC[A/G]TTTGAAACTTTTGCT | 19016 |
rs50804205 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115364004 | TTAACTTACTTTTCA[A/G]ATTATGAAGTGGTTG | 19016 |
rs50807154 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115386677 | ACCTAAAGCAGTTAG[A/T]CTCATAGAAAGTGGA | 19016 |
rs50826274 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115397376 | CAGCGAGGAGATAAT[A/G]GTGAATGTCCTGTGC | 19016 |
rs50826517 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115487127 | CATAAGGTGCTGTGC[A/G]GGTCAGAATAAAAAG | 19016 |
rs50848848 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115371711 | GTGACCACTGACTTT[A/C]CGAACCCTGTATCTT | 19016 |
rs50856352 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115473413 | TTTTTACTGACTGTG[C/T]GTGTTGTGTAGAACA | 19016 |
rs50888408 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115397461 | GAGGTGTCAATCCCA[A/G]ATCAAAGTTGGAACC | 19016 |
rs50891349 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115443006 | TGCCAGTCACATAAA[C/T]ACTTCAGCCCTCAGT | 19016 |
rs50912321 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115379992 | TTTAATATATTTTTA[C/T]TGTGTAGTTGGATAC | 19016 |
rs50926965 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Pparg | Mm_Celera | 6:115487126 | TCATAAGGTGCTGTG[C/T]GGGTCAGAATAAAAA | 19016 |
rs50931661 | snp | C/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115426213 | TTGAAAGCAGCATGG[C/G]AGCAGCTAGTCTCTC | 19016 |
rs50934594 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115419575 | AGGGCGTTAAAACAC[A/G]ATCCTAGGAGCAGAT | 19016 |
rs50947675 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115482219 | ACAATGCGTCCTGCA[G/T]CAGGCAGATGATATC | 19016 |
rs50973710 | snp | G/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115444598 | CATAAAGATTAAAAC[G/T]TAACACTTGAATCCT | 19016 |
rs50981191 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115372001 | CATTTGGTTTTGATA[C/T]GGCTATAAAGCTTTA | 19016 |
rs50990768 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115458241 | TGAACTAATACATCC[A/G]GAATTTTCTCTTTTA | 19016 |
rs50990835 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115364807 | CTTTGGCGAAATGTA[C/T]GGTTCATGTTAAGAT | 19016 |
rs50993941 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115427294 | TCTCCTCTACTTCCC[C/G]GGATGCCAACAGCCT | 19016 |
rs50995208 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115469158 | TATGCCTACCGAGCC[A/T]TTTGATGCTGTTTCT | 19016 |
rs51005218 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115402436 | GGCAGGCAAACATGA[C/T]GGCACAGAAGGCCTG | 19016 |
rs51044956 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115392174 | TACCACCAATAGTTC[C/T]GACACTAAACTTTCA | 19016 |
rs51048799 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115465361 | GACACAGCACCCAAA[C/T]CACTAGAAATCACTT | 19016 |
rs51054278 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115363803 | AAAGCATGACTTTAA[A/T]TTTTTGACGTAGAAA | 19016 |
rs51094189 | snp | A/G | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115484142 | CTGACCTGACCTCAC[A/G]CTGTAGCAAGGTTTG | 19016 |
rs51113483 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115373413 | GCTAGACATGCGCAG[A/G]CCCTTTGCTTCCTGA | 19016 |
rs51114708 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115428220 | CACCATGTAATTTAG[C/T]CCTTAATAGAGACAG | 19016 |
rs51118079 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115411140 | ATTCTACTTCTACCG[C/T]CTTGTCTGTGTCATC | 19016 |
rs51131220 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115457823 | ACTTTAGCCTTCTAG[A/G]AAACAACTGCTCAAC | 19016 |
rs51131787 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115430520 | AAACTGTGCTTGAGC[G/T]AAGTTGATCACAGTG | 19016 |
rs51139989 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115465695 | ATCAAACTAGACATC[A/G]TGAGCTATTGGATAG | 19016 |
rs51140481 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Pparg | Mm_Celera | 6:115487459 | GAATCAATGCAAGAC[A/G]ATGAGTGGGTCCTAA | 19016 |
rs51146409 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115424154 | GCTATAGGATTCTGT[A/C]TTCAGCCTAGCCCAT | 19016 |
rs51156124 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pparg | Mm_Celera | 6:115461946 | GTAAATGTGCCCCAA[C/T]CTTTGCTCACAAGTA | 19016 |
rs51169793 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115458095 | GGCCTTCAGTCTGAT[C/T]GATTAGCTATAGAAA | 19016 |
rs51173353 | snp | G/T | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115451870 | ATATGAGATCTTGAG[G/T]TTCCATCCCCAGCAG | 19016 |
rs51177627 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115363837 | ATTATGCAAGTGACT[A/G]ATTTCAGTTAGTAAG | 19016 |
rs51186731 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115470891 | TCTCTGAGGTGTGAT[A/G]AGCATTATGGTTGAA | 19016 |
rs51192664 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115402318 | TTTTCTAAAGGTGTG[A/G]AGACAGCTCACTGAA | 19016 |
rs51206455 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115419880 | AACCAGGTGAAATTG[C/T]TGACCTTAGAAATCA | 19016 |
rs51218571 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115395573 | ATGTCACCAAGAATA[A/G]GCTTTATGGTATTAT | 19016 |
rs51226232 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115402754 | CAGAACTCTAAACTC[A/G]ATAATATAAGCAAGT | 19016 |
rs51228797 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115472090 | AAGTAAAAGCTCAGA[A/G]CCATTCTTATTTTAC | 19016 |
rs51241339 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Pparg | Mm_Celera | 6:115413797 | GTAAAATTGCTGCTT[A/G]ATCCTGAGGATTCCA | 19016 |
rs51260942 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115402330 | GTGAAGACAGCTCAC[C/T]GAAGCCATGCTGCTG | 19016 |
rs51273958 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115457987 | AATAGTTACTTAACT[A/G]AAAACACCAATCTTT | 19016 |
rs51283235 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pparg | Mm_Celera | 6:115483803 | GCTAGTGGGCGGGAA[C/T]AGCCACAGACCCTTC | 19016 |
rs51287267 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115470231 | ATTCTAAGCAAGCAC[A/G]GTACTTAGGCCTAGC | 19016 |
rs51293179 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115402108 | TATAGGACAAATTAA[A/G]ATGTACATTAAATTT | 19016 |
rs51324449 | snp | C/G | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420854 | TTCTCGATTCACTGA[C/G]TGATATTTAGACCTA | 19016 |
rs51332476 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115374720 | AGAGCTTTGAGGTGA[C/T]GTTGTCATAGAATTC | 19016 |
rs51343519 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115442466 | CTCAGAAATAAAATA[C/G]CATGTAACTTATGCA | 19016 |
rs51353613 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115369924 | ACAAGAACCCATATT[C/T]GAACTGGGAATGTTG | 19016 |
rs51363735 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115462649 | TTGTTCTACAGAGGG[A/G]TTAGAGGTATAAAAA | 19016 |
rs51371659 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115374445 | TTAGATTTCAGACTG[A/G]TGATAAAGGTCTGGA | 19016 |
rs51375751 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115438056 | AACCTTTGTCAAATG[C/G]TGCTAATATGACTAC | 19016 |
rs51379644 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115481953 | AGATCTAGAGAAGGT[A/G]TCACCTGCCTTTTCA | 19016 |
rs51391251 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115415394 | CTCTTTTAAATATTA[A/C]AAAAGTCAGACAGTA | 19016 |
rs51405606 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115397391 | GGTGAATGTCCTGTG[C/G]TGTGGTTGACTTAGA | 19016 |
rs51405893 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115453799 | CTCCTGATGAGGAAT[C/T]ATTTCTGAATACAAA | 19016 |
rs51406528 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115400164 | AAGGGAAACAGGGTG[A/G]TAGAGGCATGGAGAA | 19016 |
rs51428341 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115422736 | AATATCTGTTCTAAG[C/T]CTCTCACTTTACACA | 19016 |
rs51456420 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115400755 | GGGCTGAATGTGACT[A/G]CTTAACAAATCCAGT | 19016 |
rs51478688 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Pparg | Mm_Celera | 6:115406883 | GAGCAACATTTAAGC[C/T]AGGACAGTGCAAGAA | 19016 |
rs51487985 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115432371 | CTGACTCTCACCTCC[A/G]TGACTTGAGAATCAC | 19016 |
rs51489124 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115444673 | TCTGAAAGATCAGTC[G/T]GGATAAGATCTCCCC | 19016 |
rs51495377 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Pparg | Mm_Celera | 6:115429528 | ATTTCATGCATAGTT[C/G]GGATAAATAGTGTAT | 19016 |
rs51500963 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115394629 | GAGCATCAGAGCTTG[A/G]GATAGGGTCCTGTGG | 19016 |
rs51526350 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115387218 | TTTATGACAGCCATT[C/T]AACTCTAGTTATACT | 19016 |
rs51526492 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115464239 | TGTCCCTAGGCAGTA[A/G]GAGCTACAAGTCCCA | 19016 |
rs51568655 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115418692 | CAGTGGTAGATGATC[G/T]CTCTTTTAGGTTTGT | 19016 |
rs51583424 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115390686 | TTCTTTATCTGTTGA[A/G]TAGGAAGGTGTTTAT | 19016 |
rs51586928 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115370710 | AATGCAAAAATCACA[C/T]ATATTTACACTTATA | 19016 |
rs51590403 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115466436 | CCAATCAATTTTAAC[A/G]TCATATTTTTGTGAA | 19016 |
rs51620579 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115445690 | TCATAAAATTTGAGG[A/G]GAATAACAGTAAAAG | 19016 |
rs51636305 | snp | G/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115426912 | AACTGCCTCCATCAG[G/T]CTTCTAACAGTTGGG | 19016 |
rs51637011 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115395401 | ACTCAGTAAATGTCT[A/G]TATTTTGCTAACTGT | 19016 |
rs51655257 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115373636 | GAGCCTTGAATCCAC[C/G]TAAGTCCAAAAAGGG | 19016 |
rs51690293 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115400678 | GACAGCTGAAGGGAA[A/G]CCAAGGGGAGGTGCA | 19016 |
rs51706994 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115386513 | CAGAAGGAGTGATCT[A/G]AATTCAGTTATTTTG | 19016 |
rs51725471 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115419643 | ATAATTTGTGTGATT[G/T]AATAACAAGCACACA | 19016 |
rs51727010 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115363591 | TTATACACATCAATA[C/T]TTAAGACTACTTTGA | 19016 |
rs51731266 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Pparg | Mm_Celera | 6:115391388 | ATCCATGCTTAGCAT[G/T]CATGAGGTCCAGTCC | 19016 |
rs51732088 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115411575 | CTATACAATGGAGTC[A/G]TCCTCTGTGATTACA | 19016 |
rs51736628 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115422486 | TATAGTCTAAAAATA[C/T]GTGTGAGCATTTCAG | 19016 |
rs51737675 | snp | C/T | 0.142012 | 0.225474 | downstream-variant-500B | Pparg | Mm_Celera | 6:115490881 | TGTCATCCCTCTATA[C/T]TCATGGGGTCTGGCT | 19016 |
rs51738154 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115394809 | ATGTGGTGATTGAAT[A/G]CACAGAAAGAAGATG | 19016 |
rs51747952 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115469241 | TTGAAGACACGACTC[C/T]TCCTGCAATTGGTAT | 19016 |
rs51749968 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420171 | TATCAAGGGGCCTCC[A/G]TTTCTCATCTTTTTA | 19016 |
rs51750519 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pparg | Mm_Celera | 6:115488503 | ATGTATGGAAATGTC[A/G]TGATGAAACCCACTC | 19016 |
rs51754492 | snp | A/T | 0.42 | 0.183303 | intron-variant | Pparg | Mm_Celera | 6:115413235 | TCATTTGACAATTTA[A/T]CTGTGCTGCATGGTG | 19016 |
rs51767884 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115407196 | TCAGGAGCATGTGGT[A/G]TCTGTAACACAAGAC | 19016 |
rs51778987 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Pparg | Mm_Celera | 6:115486969 | ACACTGCTACTTCCT[A/G]GGCACAGCAGGAAAG | 19016 |
rs51783794 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Pparg | Mm_Celera | 6:115449004 | CAAGACCAAGATACC[G/T]TACTTTGTATTTGCA | 19016 |
rs51788296 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115470870 | TCTGAGTCCTCTAGT[A/C]TCTCCTCTCTGAGGT | 19016 |
rs51793016 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115428177 | TAACAGTCAAATGAG[A/G]GTGAAACCCCCTGAC | 19016 |
rs51810302 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115465352 | GTTCTGAAAGACACA[A/G]CACCCAAATCACTAG | 19016 |
rs51825820 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Pparg | GRCm38.p3 | 6:115388691 | TTTCTTTTTTAAAAA[C/G/T]GTCAGGCTTGGAGAT | 19016 |
rs51845096 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Pparg | Mm_Celera | 6:115426446 | GCACAGCTTCACTAT[G/T]TTAGCTTCCTTGGAC | 19016 |
rs51852708 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115405435 | TTCTGTTGCACAGGT[C/T]TATCACTGAACCAAA | 19016 |
rs51870021 | snp | A/G | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115470585 | ACCCCTAGAACACCA[A/G]TAGAGGAGGAAGAGG | 19016 |
rs51870698 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Pparg | Mm_Celera | 6:115461284 | ACACATTTGAGACTC[A/G]AGGACAAATCAGTCT | 19016 |
rs51871288 | snp | A/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115369868 | GGAGCACCAGAAGAT[A/T]TAGGAAAAGACAGAT | 19016 |
rs51879652 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115448992 | TATATGTTTTCTCAA[A/G]ACCAAGATACCGTAC | 19016 |
rs51885793 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115451690 | GGTGGTGTTCTTTAC[C/T]ATGCCTTTGCTATAT | 19016 |
rs51887259 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115379570 | GACATGGAAAAGCTC[A/T]GTGAGTTTGTATCCA | 19016 |
rs51888285 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115414233 | CTCTACCCCCTCCCC[C/G]GGCTCCATACTGAAG | 19016 |
rs51893634 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Pparg | Mm_Celera | 6:115486421 | TGAACTGCCTTGCTG[C/G]CCCAAGTGATTTCAT | 19016 |
rs51903363 | snp | C/T | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115479371 | ATGGCCATTGCAAAG[C/T]ACCTCATTCAACAGC | 19016 |
rs51920161 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115424495 | CTAAGTAACCTCATG[C/T]TGGCTCTGATTTCCA | 19016 |
rs51925937 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115488939 | CTGTTAATGTGATCC[A/C]CTACACTAGGTTAAG | 19016 |
rs51927856 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115462606 | AGGTTACCAAGATAA[A/T]TATGACAGTGTCCCT | 19016 |
rs51943367 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115374952 | TTATGGAACTGTCAC[A/G]TAGCCTTTATTTATC | 19016 |
rs51953249 | snp | C/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115478159 | CCTATTTGTTGAATG[C/T]CCCAAACATCCAGGA | 19016 |
rs51972096 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pparg | Mm_Celera | 6:115388888 | TATGTGCTGATGACT[A/G]AGTCCATGTACTGTG | 19016 |
rs51976290 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115489468 | GTGTTTGTGCTAAGC[A/C]AAAAAACAGCAAGGC | 19016 |
rs51981362 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115464603 | ACATTCTTTACACTC[C/G]AGCTCAGGGTCCTCT | 19016 |
rs51995321 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115381914 | CTTTTTGGTGGCAGG[A/C]AACTGGTCTATCACT | 19016 |
rs51995984 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115486441 | AGTGATTTCATTGTG[G/T]TGTCAGAACTGAGAA | 19016 |
rs52006109 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115407207 | TGGTATCTGTAACAC[A/G]AGACTAACTTTAAGT | 19016 |
rs52008325 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115394527 | AGTACGGAAGAAGTC[A/G]GACATTTCAATGATA | 19016 |
rs52014380 | snp | A/G | 0.18 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115487266 | TGGATCTGGATGTTG[A/G]AGGAATTTGAAATAG | 19016 |
rs52038298 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115368191 | TCTTCATGAGTTAGT[C/T]CCAGCAGACAGCTAA | 19016 |
rs52100350 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115387617 | GACTCATTTTTATTA[A/G]CTTTAATTACATTTA | 19016 |
rs52137641 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115459829 | CAATGTACATATTGA[C/T]TCATATTCTGTCTAA | 19016 |
rs52144431 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115387534 | CCCAGGGCTTTCCAG[A/G]CTCATAAGTCTACAC | 19016 |
rs52188745 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Pparg | Mm_Celera | 6:115410229 | TCAAGGATTTTATGA[C/T]ACTGTGTTGCACTAT | 19016 |
rs52205505 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115482680 | ACCTGCCTTGTATGC[A/G]TGAAGACAGGAATTC | 19016 |
rs52216985 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Pparg | Mm_Celera | 6:115486231 | CTTCTTAACTTTGGA[A/G]ATTTTTTTCTTTATT | 19016 |
rs52221967 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Pparg | Mm_Celera | 6:115445422 | TAAGAATCATTTTTT[A/T]AAAGGCAAATAGAAA | 19016 |
rs52265252 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115474966 | TGTTTGTTTTTTGTG[G/T]TTTTTTTTTTTGTTT | 19016 |
rs52330813 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115444299 | GTAGTGTAGGACTAC[A/G]AATGGTGAGAGACAG | 19016 |
rs52338233 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Pparg | Mm_Celera | 6:115376814 | CTGAATGGCCAGGAC[C/T]TCTGGGCCTGTTCTC | 19016 |
rs52351179 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pparg | Mm_Celera | 6:115380188 | ATTCATGCATGAACT[C/T]CTAGGGTCACACACA | 19016 |
rs52351811 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115371031 | GTATGTATGTATCTT[A/G]TATTGGTCTTGTGGC | 19016 |
rs52415173 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Pparg | Mm_Celera | 6:115416930 | TCTATATCATGGAAA[A/T]TTTTACATTAATTAT | 19016 |
rs52456724 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Pparg | Mm_Celera | 6:115403069 | CAGTAAATGGTCATA[A/C]TGTCTATATTATGCT | 19016 |
rs52503500 | snp | A/T | 0.32 | 0.24 | intron-variant | Pparg | Mm_Celera | 6:115457689 | AATATTTTCCTTTTG[A/T]CATTGGAAATTAATC | 19016 |
rs52504327 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pparg | Mm_Celera | 6:115370828 | TTCCAGAAGGAATTG[A/T]CCTAGGTTATATATT | 19016 |
rs52565575 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Pparg | Mm_Celera | 6:115403077 | GGTCATAATGTCTAT[A/T]TTATGCTTGAGTGAG | 19016 |
rs52582997 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pparg | Mm_Celera | 6:115444269 | GCAATTGCTTTCTTG[A/G]TGGAGGATTTTAAAG | 19016 |
rs107966595 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115413307 | ACGGAGTAGAGCTGC[A/C]CCTCAAGCTCACAGT | 19016 |
rs108119229 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115412967 | TACATATGTGGAAGC[A/T]AATAAGTAAATCTTT | 19016 |
rs108163022 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115413012 | TCAAGAACATGAGTG[C/T]CACAGTAACTGCACA | 19016 |
rs108604091 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115412854 | CACACACGTTGGGTG[A/G]TTCACAAGTGTCCAT | 19016 |
rs108740353 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115453118 | AGCCCAAAGTATATT[C/T]CCAGTACCCTTCCTC | 19016 |
rs211712492 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115462496 | ATATGAACTGACTGA[A/G]AACAGGGCCTATGTT | 19016 |
rs211727621 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115395008 | AATTTTTGACTGATA[A/T]AAGGGATAGAGGTGT | 19016 |
rs211787562 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115476028 | TCTCATCTGACCCAC[A/G]CAACAGTGAAAGATA | 19016 |
rs211852973 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115486317 | GCCATGATACATATA[G/T]AGAGGGTCAGAAGAT | 19016 |
rs211861480 | in-del | -/CCCCTGTTCCAGA | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115361895 | CGCGGAACAGGGTTG[-/CCCCTGTTCCAGA]CCCTGACAGGAAAGC | 19016 |
rs211876077 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115405825 | CCAGCTCCCCATGTG[C/T]ATTCTCTAGAGAATA | 19016 |
rs211932349 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115416447 | CAGCTTCAACTGAGC[C/T]AAGAAGGCAGTTGTT | 19016 |
rs211934362 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115429479 | ATCACCACCACATTC[C/T]TTTCTTTTGTTTCTC | 19016 |
rs211935502 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115417532 | GATCCCTGAGTGGGA[C/G]AGTTTCTGGATGGTC | 19016 |
rs211939734 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115363731 | GGCAAATTACACTTT[A/T]AAAAAAATCATATCT | 19016 |
rs211972305 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115439412 | AAAAAGGAAAAACTT[A/C]TGTTTCTTGTAGCAA | 19016 |
rs211973628 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115428545 | TTTAAAATAAATCTC[C/T]TTTTTTAAAGTCTGC | 19016 |
rs211980883 | in-del | -/TTATTGTTGTTGTTGTTG | | | intron-variant | Pparg | Mm_Celera | 6:115429155 | GGTTTTGTTTTTGTT[-/TTATTGTTGTTGTTGTTG]TTGTTGTTGTTGTTG | 19016 |
rs212013804 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115374982 | CAAATGGTAGCCAGA[C/T]ATTAAAGAGAGTCAT | 19016 |
rs212045646 | in-del | -/T | | | intron-variant | Pparg | Mm_Celera | 6:115469753 | TTTTTTTTTCTGTTC[-/T]TTTTTTTTCCCAAAC | 19016 |
rs212065789 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115438785 | CAGTCCAAAACAATG[A/C]ACAAAGGCTATTCGT | 19016 |
rs212148204 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115447858 | CAACTCTGCCCCATG[A/G]AAGTCACAATTTTAA | 19016 |
rs212165006 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115488584 | TAAAATAGATTCCAG[A/G]CTATAGTAGATTATC | 19016 |
rs212179254 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115460525 | TCTCCTTCTCCCTCC[C/T]CTTCCCCCCCTTCTT | 19016 |
rs212200359 | in-del | -/AG | | | intron-variant | Pparg | Mm_Celera | 6:115441232 | GGGGGGGGGGGGGGA[-/AG]CACACTTAATTCTCT | 19016 |
rs212204999 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115362974 | GGGTAGGAACGGATA[C/T]ACGCTATGACTACTC | 19016 |
rs212207741 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115474758 | CATGTTCTAAGCTTC[G/T]ATTCTGTGCAAAACA | 19016 |
rs212210604 | in-del | -/AGGATTGG | | | intron-variant | Pparg | Mm_Celera | 6:115440091 | ACTTTTCAAACTACT[-/AGGATTGG]AGTTAGACAGTTTTT | 19016 |
rs212214228 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115394291 | TTTACATATCCAGTA[A/C]TGTGCTAGACAGAAT | 19016 |
rs212236064 | in-del | -/A | | | intron-variant | Pparg | Mm_Celera | 6:115488569 | TTTACAATATATAAT[-/A]AAAATAGATTCCAGG | 19016 |
rs212244679 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115374476 | ATGCAGATGCAGGAG[A/T]ATGGGCTTTGTCTTA | 19016 |
rs212305015 | in-del | -/TG | | | upstream-variant-2KB | Pparg | Mm_Celera | 6:115360572 | AAATAAAAATAAAAC[-/TG]AGATTAAAAATAAAA | 19016 |
rs212305682 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115393580 | AGGGTACATGAAGCA[C/T]AAATGAACTTTGGGC | 19016 |
rs212313908 | in-del | -/CT | | | intron-variant | Pparg | Mm_Celera | 6:115471497 | AAGTCATATAGTTAA[-/CT]AGCACTCACCCAGCA | 19016 |
rs212395725 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115461183 | AACATCTTTTCCCCT[A/C]TAACTCCAAGCAAGG | 19016 |
rs212400693 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115483900 | AAGCACCCCCAAGCT[C/T]TTTCATTTCTACAAG | 19016 |
rs212407870 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115413409 | ACAGCATCTGAATTC[C/T]AGAGATACTTGTTGG | 19016 |
rs212415842 | snp | C/T | | | downstream-variant-500B | Pparg | Mm_Celera | 6:115490902 | GGGTCTGGCTCCAGG[C/T]CTCCTGAAGGAGCCA | 19016 |
rs212422108 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115380550 | tacaagagcaacaga[C/G]acacaaaaAAGTGTA | 19016 |
rs212432640 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115401468 | CGTCAGGCCTTGGAG[C/T]CTCCCCTTGAGATGG | 19016 |
rs212453324 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115444625 | TCCTTAAGAGACACA[C/T]TCCTAACAGAGCAAT | 19016 |
rs212456095 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115427782 | CACCATTGCTCCCTT[C/T]AGACACACCAAAAGA | 19016 |
rs212467276 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115487420 | AGCACTTAACAGAGC[A/G]AGCAACCTGCAGGGC | 19016 |
rs212492078 | in-del | -/TTAT | | | intron-variant | Pparg | Mm_Celera | 6:115468704 | GTTAGTTGAACTTTC[-/TTAT]TTATCTCCTTTATTG | 19016 |
rs212540547 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115456327 | GCAATTAACCATTAT[A/C]ATCTCAGTGGCATGA | 19016 |
rs212555638 | in-del | -/A | | | intron-variant | Pparg | Mm_Celera | 6:115376568 | TCAGACATCTCAAGT[-/A]AAAAAATTCATGTCT | 19016 |
rs212576471 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115380461 | TAATGGTAAAATCTC[G/T]GGGTTTTACAATTGT | 19016 |
rs212586168 | in-del | -/ACACACACACACACAC | | | intron-variant | Pparg | Mm_Celera | 6:115440289 | AATGTTCCCAAACTT[-/ACACACACACACACAC]ACACACACACACACA | 19016 |
rs212616527 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115379212 | TTGTATGCCTTTAAT[C/T]CCAGTACTCAGAGGC | 19016 |
rs212617314 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115468803 | ATATATTAACATGCC[A/G]ATGGATTACTAAAAG | 19016 |
rs212663033 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420197 | TTTTACACTCCTTCT[-/A]AAATAGTATCACTCT | 19016 |
rs212663106 | in-del | -/A | | | intron-variant | Pparg | Mm_Celera | 6:115369351 | TGCTAGATTACTTAG[-/A]AAAAACTCTGTGCTG | 19016 |
rs212678945 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115414229 | ACACCTCTACCCCCT[C/T]CCCGGGCTCCATACT | 19016 |
rs212689431 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115368583 | ATTGTCTCTTTCTTA[C/T]GGTTGATAATTACCC | 19016 |
rs212689843 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115398206 | TGATTTCTACCTTTT[A/T]AAATTTTGCCTATCC | 19016 |
rs212715149 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115389741 | ACAGCAGTGACATCT[C/T]TCGTTTTATTTTAGT | 19016 |
rs212727722 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115467370 | GAGAAAAACTTAGGG[A/G]CCCCATAGGAATCAA | 19016 |
rs212766981 | in-del | -/G | | | intron-variant | Pparg | Mm_Celera | 6:115462216 | TTATTTAATTTTTTT[-/G]GGGAAGGCCTTGCAC | 19016 |
rs212775896 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115409941 | CATTTTGATTGGTTC[A/G]CGACTGCCTATAAAT | 19016 |
rs212791113 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115479287 | TGTGTCTTCGTTTCT[C/T]GTGCTCTAGAGGAAC | 19016 |
rs212802899 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115478449 | CCACCACCACCACCA[C/T]CATCATCATCATTAC | 19016 |
rs212856275 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115422629 | AAATCTACATTTTTT[C/T]CCCAAAGAATTGCAA | 19016 |
rs212942451 | in-del | -/T | | | intron-variant | Pparg | Mm_Celera | 6:115394032 | CCCAATAGGCTGCAG[-/T]TTTTTTACTCTTTGT | 19016 |
rs212942975 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115432314 | TCAGTGTCTCAATAA[C/T]TCCCTTTCAAAGGCA | 19016 |
rs212959680 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115454931 | AGCATCTTCCCACCT[A/C]TGAAAGGTTTCACGA | 19016 |
rs212981868 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115431088 | ATTATACATAACTTC[A/G]TATTATATCTTTAAT | 19016 |
rs213030813 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115442074 | CTCTTAAACAAGAAA[A/G]GCTTGATAGACTATA | 19016 |
rs213035528 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115398832 | CAGTCACTTCTAAAG[A/C]TGTATGCCACCATCT | 19016 |
rs213038986 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115378074 | TGAATGAAAGTCTGT[A/G]ATTTCCTGTTTAGAA | 19016 |
rs213069276 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115453222 | CTTGATAATAAAGTC[A/G]TCATTTGACTTTAAC | 19016 |
rs213073062 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115480445 | ACTGAGCAAACAGTG[G/T]TGTCTGAGGCAGACA | 19016 |
rs213074291 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115430493 | AAACATAAAGATTAA[A/C]AGAAGAACCACAAAC | 19016 |
rs213105127 | in-del | -/AA | | | intron-variant | Pparg | Mm_Celera | 6:115489311 | AAAAAAAAACAAAGG[-/AA]AAAAAAAAACGGTAG | 19016 |
rs213181355 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115388812 | TAAAAGCAATAGTCT[A/G]CTTTATAGCAAAGAC | 19016 |
rs213209056 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115464887 | AAGCCTACTTCACCG[C/G]CAGAAAAGTAAAGAA | 19016 |
rs213214023 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115388254 | ACCTAATTTACTAAG[C/T]CAGGTTTTAAGTGCT | 19016 |
rs213219773 | in-del | -/C | | | intron-variant | Pparg | Mm_Celera | 6:115459215 | CCTAGGGATCCTATG[-/C]CCTCTTCAGGCCTTA | 19016 |
rs213238901 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115463958 | AGAACTAAGCTACAG[C/T]CCCAAGCCACAAAAG | 19016 |
rs213251471 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115408872 | ATGCTTATTTAAAAG[A/G]TGTCAACCAAGAAAA | 19016 |
rs213263187 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115487760 | ATATAGCTCTTAAGT[A/T]AAAAAAAAAATAAAG | 19016 |
rs213281124 | in-del | -/TT | | | intron-variant | Pparg | Mm_Celera | 6:115403278 | TGCTTGCTTTCCACA[-/TT]TTTTTTTTTGAGACA | 19016 |
rs213327553 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115414477 | CTAGAAACTAGGTTT[A/T]AAAATGTAAAATCTA | 19016 |
rs213330194 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115428370 | AACACATAGTAGTCA[A/G]CTTGTTGACTTATTA | 19016 |
rs213369337 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115427853 | TGGTTGCTGGGAATT[C/G]AACTCAGGACCTCTG | 19016 |
rs213438584 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115468969 | gaaagaaggaTCATT[C/T]TTTGTCCAGCAAAGC | 19016 |
rs213458638 | in-del | -/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pparg | Mm_Celera | 6:115361541 | ACACTCCGACAGGAC[-/G]GGAGAGTGACCAAGT | 19016 |
rs213459105 | in-del | -/GTTGTTGTTTTG | | | intron-variant | Pparg | Mm_Celera | 6:115468433 | CCAAGCCAGGTTATA[-/GTTGTTGTTTTG]GTTTGGTTTGGAAAT | 19016 |
rs213462107 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115373477 | GGAGGTTTGAGATGT[A/G]CTCTCATTGAATATC | 19016 |
rs213498382 | snp | G/T | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115365541 | GTAGTCTCCTTCAGC[G/T]CCATAGTTTATTACC | 19016 |
rs213515155 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Pparg | Mm_Celera | 6:115360950 | CGGGCGCGGGGCCTC[C/G]GGCCTCACCCTGGGC | 19016 |
rs213537097 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115440918 | TGAGCCACGGGCAAA[A/C]GCAGTACTTGCCTCA | 19016 |
rs213553635 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115384891 | TGTCAGAGAACCATA[C/G]CAACTGTTGCTGCAG | 19016 |
rs213557305 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115436261 | AGAAAAGTAAGGAAA[A/C]TATAACTCAGTAGTA | 19016 |
rs213564752 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115460392 | CCATGTCATATTCCA[C/T]GTCATATTCTCCCCA | 19016 |
rs213596795 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115459568 | GTCTGTGAAGCAGTA[C/G]ATGATTCTGGCAACT | 19016 |
rs213616424 | in-del | -/T | | | intron-variant | Pparg | Mm_Celera | 6:115472234 | ATCTGCTTTGAGTGA[-/T]TTTTTTTATAGTGAA | 19016 |
rs213634110 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115372758 | AGCTGGAAATGGTTT[A/G]TAACAAAGCACAACA | 19016 |
rs213648293 | in-del | -/AAA | | | intron-variant | Pparg | Mm_Celera | 6:115424250 | TGCTACTGTAGAAAT[-/AAA]AAAAAAAAATGTTTA | 19016 |
rs213663382 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115446884 | CTACAGAGTGCCAAG[A/G]GAAAGAATGTATACA | 19016 |
rs213711366 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115391871 | TTTTATCTTCCAGGC[C/T]TGGAATGAAAGCAAT | 19016 |
rs213749216 | in-del | -/T | | | intron-variant | Pparg | Mm_Celera | 6:115432011 | TCTGTTGGTTAAATA[-/T]TTTTTCTTTTATTTC | 19016 |
rs213790377 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115478393 | CATTGAGCATGTGCA[A/G]AACTGGGCATGTTCA | 19016 |
rs213792599 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115413252 | TGTGCTGCATGGTGT[A/C]TGAGCTCCCATTTCT | 19016 |
rs213858878 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115425276 | ATGAGTATCTTAAGA[A/C]GAAAATAATCAAACT | 19016 |
rs213899455 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115425419 | GTTTGCCAGGCAAGC[A/G]CTCAGCCGCTGAGCT | 19016 |
rs213902358 | in-del | -/CTACTTGG | | | intron-variant | Pparg | Mm_Celera | 6:115386314 | CACGATGAGGAAAGA[-/CTACTTGG]CATCAGTCAGAAAGT | 19016 |
rs213919918 | snp | A/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pparg | Mm_Celera | 6:115361599 | GCTGAGGAGAAGGCA[A/T]ACTCTTGACAGGACC | 19016 |
rs213926826 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115482387 | ATAAATCCTCAGCCC[A/G]GGATTGGAAAGAGGG | 19016 |
rs213937062 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115424446 | GTCCCTTTCATCTCA[C/T]TTCTTTTCTTTTTTA | 19016 |
rs213957744 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115437327 | GCTGGGTCCATGAGG[A/G]GGGATTTTGAGGCAA | 19016 |
rs213962759 | in-del | -/TTAG | | | intron-variant | Pparg | Mm_Celera | 6:115447934 | TGAGCATTTAGACAC[-/TTAG]TTAGGGAATTTCTGT | 19016 |
rs213994655 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115447677 | TTTACAGTAATGCTT[A/C]TGTAAGCTCATAATA | 19016 |
rs214010103 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115434085 | TCAAATGGGAAATGA[C/T]GATTATTTCAAAATG | 19016 |
rs214013462 | in-del | -/TTGGTTTGGTTTAGTTTGGG | | | intron-variant | Pparg | Mm_Celera | 6:115453480 | TTGGTTTGGTTTGGT[-/TTGGTTTGGTTTAGTTTGGG]TTTTTTGAGACAAGG | 19016 |
rs214053645 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115489796 | AAGAAACAGGGCGGT[A/G]ATGGGGTCTTGGCTC | 19016 |
rs214085245 | in-del | -/AAA | | | intron-variant | Pparg | Mm_Celera | 6:115395436 | TGTTTTTTGAAAGAC[-/AAA]AAAAAAAAAAAACCA | 19016 |
rs214146174 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115408757 | GGAGTTAACAGTATG[C/T]ACTTGGAGAGGTAAA | 19016 |
rs214182639 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115407859 | ATTCTATTGGTTTGG[G/T]TTTTGTTTGTTTTCC | 19016 |
rs214237682 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115392752 | ATAATGCAACTAAAA[C/T]TAAATTATTCAAACA | 19016 |
rs214265834 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115419193 | TTTAAAGTCCATAAG[A/G]GTACACACATTTTAT | 19016 |
rs214282274 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115400918 | AGTTTATGACCATTA[A/G]CTTTGAGTTGCCTGT | 19016 |
rs214286963 | in-del | -/A | | | intron-variant | Pparg | Mm_Celera | 6:115408811 | TCTAGGTTGTGTGAC[-/A]TCAACTCCATTCAGT | 19016 |
rs214292733 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115370434 | AGCTCTCCTCTTTTA[A/T]TTTTTCTCCTTAAAA | 19016 |
rs214303784 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115417945 | CTGAAATCCTAACAC[C/T]TGGGAAGTGGAGGCA | 19016 |
rs214332322 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115389063 | tcaagttcaaggcca[C/T]cttgagcatagggag | 19016 |
rs214351547 | snp | C/G | | | downstream-variant-500B | Pparg | Mm_Celera | 6:115490675 | AATTAGGTTAGACTA[C/G]AGGGTCAGTGAGCCC | 19016 |
rs214367245 | in-del | -/C | | | intron-variant | Pparg | Mm_Celera | 6:115379892 | TGGTCTCTCTTTCTA[-/C]CTTTACGTGAACTAC | 19016 |
rs214397433 | in-del | -/C | | | intron-variant | Pparg | Mm_Celera | 6:115428544 | ATTTAAAATAAATCT[-/C]CTTTTTTAAAGTCTG | 19016 |
rs214458963 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115487526 | TTAAGAAGAAAATCT[A/G]TATATTCTAACAAAC | 19016 |
rs214488166 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115375021 | TCAGTGTAAGTAAAG[A/G]ATTGTAATATCTATA | 19016 |
rs214509580 | snp | A/G | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115450554 | GTATATTTATATAGT[A/G]CAGATGCATGTATGT | 19016 |
rs214525568 | snp | G/T | | | upstream-variant-2KB | Pparg | Mm_Celera | 6:115359085 | AAAATATCTAGGGTA[G/T]AAAAGTCTATCCAGA | 19016 |
rs214542696 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115485559 | GGGAACTGAGCCCAA[A/C]AAATTTAATAGTCAG | 19016 |
rs214545313 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115462070 | CTGGAGAAAAGCAGT[A/G]TCCTAAAGAGAGCTA | 19016 |
rs214556893 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115434718 | GTATCTTCCGCTCTT[A/G]ATTACTCTTCTTTAA | 19016 |
rs214594754 | in-del | -/TAAA | | | intron-variant | Pparg | Mm_Celera | 6:115467231 | TGATGGGGAAGATGT[-/TAAA]GTCTCTTTAAATCCT | 19016 |
rs214613009 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115386549 | AGAATTAAATGCTAA[A/G]TATTTGGAATTTGAA | 19016 |
rs214624892 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115371606 | CTGTGGAATATTGAG[A/G]GAACATCAATTTAGG | 19016 |
rs214659885 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115430223 | ATCCTTCATAAAATA[C/T]GTGTGTGCTAAAGAT | 19016 |
rs214661432 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115445268 | GAGAAACTCAGTGCC[A/G]CAGACTTGTTATCTG | 19016 |
rs214729559 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115388398 | TTCAGTTAAGAATTT[A/G]TTAGTGGAAGTACTT | 19016 |
rs214757500 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115440787 | CTGGCAAGCATTACT[A/T]GATAATAAGTAAGAA | 19016 |
rs214764355 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115415998 | AGCCAAGAGCCTGAA[A/G]TCTAAGCTTTCTGGT | 19016 |
rs214900031 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115445335 | CCCAAACAACAACAA[C/T]AATAATAATAGTTTA | 19016 |
rs214904561 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115371660 | GCAGATGTGGCCAGT[G/T]TGTTTACTGTATCCT | 19016 |
rs214913917 | in-del | -/GGCCTAGG | | | intron-variant | Pparg | Mm_Celera | 6:115372661 | AACAGGCTCCATAAT[-/GGCCTAGG]GGCCTGAGCCCTGTT | 19016 |
rs214941434 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115444706 | GCTCTGAGTAAACAC[C/T]ATCTGCCCTCAGTTC | 19016 |
rs214941510 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115457904 | AATTTAGTTCCCTGA[C/T]AGAACATTTGCCTAG | 19016 |
rs215002268 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115394792 | TCAGGATCAGTGACA[C/T]CATGTGGTGATTGAA | 19016 |
rs215009656 | snp | A/G | | | intron-variant | Pparg | GRCm38.p3 | 6:115483539 | GAGAGGTTCATAAAT[A/G]TTCCCAAGGTCATCA | 19016 |
rs215026792 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115456502 | CTGGAAATGGTCTCT[A/G]TGCTTATAAACACTG | 19016 |
rs215032774 | in-del | -/A | | | intron-variant | Pparg | Mm_Celera | 6:115367973 | AAGTAAATGTAATTT[-/A]AAAAAAACTTAAATC | 19016 |
rs215041664 | snp | A/G | | | intron-variant | Pparg | GRCm38.p3 | 6:115481354 | GTTCTTCAgaaagga[A/G]aggagaggagaggag | 19016 |
rs215055255 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115475768 | AGAGAAATAAAAGTA[C/T]ACAGGCAAACATGCA | 19016 |
rs215057396 | in-del | -/TTGTTT | | | intron-variant | Pparg | Mm_Celera | 6:115413445 | TTGTTGTTGTTGTTG[-/TTGTTT]TTGTTGTTGTTCCCA | 19016 |
rs215137742 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115429516 | TATCAATGAGAAATT[C/T]CATGCATAGTTCGGA | 19016 |
rs215148139 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115363882 | ATAAATGATTTTTTT[A/T]ACTTTTAAGTCTCTG | 19016 |
rs215156375 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115410981 | AAGGCCCCCAAGAAA[C/T]ACAGATTTTGTTTCA | 19016 |
rs215185032 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115439540 | GGGAAGACTGGCCAG[A/G]GTTTCCATAACACTT | 19016 |
rs215185356 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115489220 | GTAGCTGCAGACTGA[C/T]AGGCTGAACCAGGAA | 19016 |
rs215188568 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115402945 | ACATTTTGATCAATG[A/T]CTTAATATATAAGCC | 19016 |
rs215214713 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115484416 | GAAATGGTGGAGTAA[A/G]TTGGAAAAGAAGTTA | 19016 |
rs215220125 | in-del | -/TGA | | | upstream-variant-2KB | Pparg | Mm_Celera | 6:115359519 | CTGAGTGTGGGATGC[-/TGA]TGACCCAAGTCAACA | 19016 |
rs215228289 | in-del | -/GG | | | intron-variant | Pparg | Mm_Celera | 6:115465251 | AGAGAGAGATGGAGA[-/GG]GAGAGAGAGAGAGAG | 19016 |
rs215235376 | in-del | -/C | | | intron-variant | Pparg | Mm_Celera | 6:115367895 | CAATCTGAGTTTGGT[-/C]CCTAGGACCCACATG | 19016 |
rs215244026 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115435013 | AAGACTCAGAGGTCG[A/G]TTAATATTAACCAGT | 19016 |
rs215250168 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115410005 | CTCTGAGGGCAGCAG[C/T]ACATCATGATATTTC | 19016 |
rs215386143 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115368378 | GTTACAGCAACTCAA[C/T]GAAGCTCTGTTAGAA | 19016 |
rs215467523 | in-del | -/AAA | | | upstream-variant-2KB | Pparg | Mm_Celera | 6:115359802 | CAAAAAACCAAAACC[-/AAA]AAAAAAAAAAAAAAA | 19016 |
rs215469332 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115378886 | GAGCCTAGTTTTATA[A/G]TATTTGTGTTACCAG | 19016 |
rs215469413 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115367119 | CTTACCATGTCCTAG[A/G]ATGTAAGAGTAGGTT | 19016 |
rs215493551 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115454573 | TAAAGCAATCTCCTT[A/T]AAAAAGTCACATAGT | 19016 |
rs215503709 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115378091 | TTTCCTGTTTAGAAC[A/G]TGGTTTGTTTGTTTG | 19016 |
rs215511198 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115478245 | TACCCCAGTTTACAG[A/G]TGGAGAAAATGGAAC | 19016 |
rs215529413 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115453324 | GAAGTTCTAGGTCAG[C/T]CATGACAACATAGTT | 19016 |
rs215560843 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115474820 | AGAAATAGCAGTATG[G/T]CAAGGGTTACTATCA | 19016 |
rs215561249 | in-del | -/CTG | | | intron-variant | Pparg | Mm_Celera | 6:115362879 | TCTGTGGGAGTCTTC[-/CTG]TCGTCCATAGCTAAG | 19016 |
rs215584854 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115467707 | AGTACCTTTGTTTAT[A/C]CACTGAGTAACTGTT | 19016 |
rs215596619 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115403896 | GCTGCGATGCTTTAA[C/T]ACGGTTCCCCATGCT | 19016 |
rs215610054 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115486211 | TTTCCTTGAAGCTTT[A/G]GTGGCTTCTTAACTT | 19016 |
rs215641574 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115469097 | CTAACAAACCTAGAT[G/T]GTCCCCTGAGCATGT | 19016 |
rs215655839 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115485216 | AAGGGAGCTGTTGAG[A/G]AAGGTGAGAAGAGAA | 19016 |
rs215659539 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115480819 | CAAGAGTCCAAAAGC[C/T]CCACTCCCCCACTTC | 19016 |
rs215661276 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115398917 | TTCCAACACATAAAC[C/T]TTTAGGGAGGAACAG | 19016 |
rs215729645 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115362645 | GTGTCCCTTTTTAGC[A/C]GGATGAAGGACAAAA | 19016 |
rs215733901 | in-del | -/A | | | intron-variant | Pparg | Mm_Celera | 6:115473658 | TCGGTTCATTTTAGT[-/A]ATGATGTGTGTAACT | 19016 |
rs215759791 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115438641 | AGTATATATATATAT[A/C]TCAAAGGGTGTGAAG | 19016 |
rs215811018 | snp | C/G | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115361842 | CGGAGGGCCACAGTG[C/G]TTCCCTGAGAGGGTG | 19016 |
rs215811504 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115374347 | ATCGTGACTAAACAC[A/G]GCCCCAGGGGCCTCC | 19016 |
rs215843785 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115437691 | ATGCCTTCACTCTCT[A/G]TGTACTAGTCCTATG | 19016 |
rs215845776 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115373608 | TCAGAGAAAGATAGA[G/T]TACCTTAGCTAGGAG | 19016 |
rs215846711 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115448694 | CAATAGCTTGCATAG[C/T]TTGTGCAAAGCCTTG | 19016 |
rs215924749 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115447782 | AGAAGGAGATAGAAT[C/T]ACATGTAAGATTTTA | 19016 |
rs215944829 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115391434 | AAAATAAACCTAACC[C/G]CCCCCTCAAGCAACT | 19016 |
rs215948992 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115432348 | ATACTTTACTCCAGG[A/G]CCCTCTTCTGACTCT | 19016 |
rs215973398 | in-del | -/T | | | intron-variant | Pparg | Mm_Celera | 6:115476220 | AGTAACAGACAAGAG[-/T]TAAAACTGGCCCACA | 19016 |
rs216000054 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115470552 | TTTTTGTTAATATGC[A/G]TTATAATACACTATG | 19016 |
rs216044452 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115484160 | GTAGCAAGGTTTGAA[A/C]AAACACAAAGAGTAA | 19016 |
rs216045357 | in-del | -/T | | | intron-variant, downstream-variant-500B | Pparg | Mm_Celera | 6:115463644 | GGCTGAGCAGGTGTG[-/T]TAAGCTGTTGTGTCC | 19016 |
rs216096894 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115401186 | AAGTGTTGGGGCCTC[A/G]GACCAGCTAGTGTAT | 19016 |
rs216148741 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115398280 | TACTCACGGTTTGTT[C/T]TCTTTGCACAATGTC | 19016 |
rs216154566 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115483798 | GAGAGGCTAGTGGGC[A/G]GGAATAGCCACAGAC | 19016 |
rs216212708 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115412763 | GATTATTGAAACTGA[A/G]TGTCAGGGTGAGGGA | 19016 |
rs216215640 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115388862 | AACTTAAATAAATTA[C/T]AGCACTGATATATGT | 19016 |
rs216228134 | snp | C/T | | | downstream-variant-500B | Pparg | Mm_Celera | 6:115490713 | CGGCCTGGCCCCACC[C/T]GCCCATCACTACCCT | 19016 |
rs216229933 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115479367 | GCTCATGGCCATTGC[A/C]AAGCACCTCATTCAA | 19016 |
rs216240395 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115489814 | GGGGTCTTGGCTCTT[C/T]GGTAAAGCATGTGCC | 19016 |
rs216267135 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115474863 | CTTTCATTTTGTGCT[A/G]TCTTTGTGCATTGGG | 19016 |
rs216275445 | in-del | -/T | | | intron-variant | Pparg | Mm_Celera | 6:115382410 | ATAATATTAGCTGAC[-/T]TTTTTTTAAAAGTCA | 19016 |
rs216282612 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115417233 | TGATGGTCGACTAGG[C/T]CATCCTCTCCTACAT | 19016 |
rs216410421 | in-del | -/TT | | | intron-variant | Pparg | GRCm38.p3 | 6:115375868 | ATCCAACTCTGTGTC[-/TT]TTTTTTTTTTTTTTA | 19016 |
rs216432901 | snp | A/G | | | intron-variant | Pparg | GRCm38.p3 | 6:115398097 | TTACAGTATTGCATG[A/G]CTGTCTCATATATAT | 19016 |
rs216467799 | in-del | -/G | | | intron-variant | Pparg | Mm_Celera | 6:115383523 | GTTTAATGGTGTATT[-/G]GGTTATTTCTAGAGA | 19016 |
rs216504153 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115396466 | CTTTTTCATTATGGA[A/G]TTTCAAGCTTGGCAG | 19016 |
rs216531761 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115427937 | CTCAGATCTTACCTT[C/T]CAGTAAGAATAGCCT | 19016 |
rs216542845 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115408868 | ATAAATGCTTATTTA[A/C]AAGGTGTCAACCAAG | 19016 |
rs216622260 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115487272 | TGGATGTTGAAGGAA[A/T]TTGAAATAGAAGTAC | 19016 |
rs216624867 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115408035 | TCATACAGTAACATG[C/T]TGTCACTGTAATGTT | 19016 |
rs216693749 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115485263 | AGGAGCTCCCAGTGC[C/T]CGTGAGGAGCAGAAG | 19016 |
rs216722194 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115483994 | TGTTTTCAACTGTGA[A/G]AGGGAGAACTTGCCC | 19016 |
rs216756594 | snp | C/G | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115365138 | AGCTGAGATCCTAAA[C/G]ACAGCCTACCCAGCT | 19016 |
rs216782329 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115440869 | TTATCTGTGTGGCTC[A/G]GGGTTAGAGCCTAAT | 19016 |
rs216789890 | snp | A/T | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115364063 | TTGTTAAAATAATTT[A/T]CCCAAAAGTCTGAAT | 19016 |
rs216848293 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115459736 | GGACAGCACTCTACC[A/G]CTGATCCACATGCCC | 19016 |
rs216860731 | snp | A/G | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115451678 | TGTATTTTTGTTGGT[A/G]GTGTTCTTTACCATG | 19016 |
rs216860906 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115439702 | GGGTGGTACTAGAAA[G/T]GCAGTAGTGCACTCA | 19016 |
rs216863227 | in-del | -/T | | | intron-variant | Pparg | Mm_Celera | 6:115381260 | ATGGCTTGTTTTAAA[-/T]TTTTTTCTAATGCCT | 19016 |
rs216872379 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115472305 | GTAAATTTAATCTAA[C/T]GCTGTAAGCTTAGTT | 19016 |
rs216877130 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115392908 | GTCACCCTCAGGTGT[C/T]CTTATTCAGGAACCA | 19016 |
rs216890104 | snp | A/G | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115450702 | GGTCAATGAGCCTCA[A/G]GGTGCCTCTGGTCTT | 19016 |
rs216919579 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115428466 | GATATATGTGTATAT[G/T]ATATATTATATATAG | 19016 |
rs216944106 | in-del | -/AAGG | | | intron-variant | Pparg | GRCm38.p3 | 6:115468898 | TAAAGAAAGAGTAGA[-/AAGG]AAGGAAGGAAGGAAG | 19016 |
rs216962907 | in-del | -/TTGTTTGT | | | intron-variant | Pparg | Mm_Celera | 6:115401878 | ACAACTGTTTATTTG[-/TTGTTTGT]TTGTTTGTTTGTTTG | 19016 |
rs216963976 | in-del | -/AAAA | | | intron-variant | Pparg | Mm_Celera | 6:115434862 | AAACAGAAAAAGAAG[-/AAAA]AGAAGAGAAAAGAAA | 19016 |
rs216969117 | in-del | -/AC | | | intron-variant | Pparg | Mm_Celera | 6:115443244 | TTGTTTCAAAAAAAA[-/AC]CAAAAACAATGAAAA | 19016 |
rs216988443 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115394936 | TTGAATTCATAGAGA[C/T]CTGCCTGCCTCTGCC | 19016 |
rs217017751 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115405582 | AAGTTAACTATTAAG[A/G]TTTACTTTGGACTAT | 19016 |
rs217019714 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115394483 | TGGGCTTGTTAACCA[C/T]AAACCCTCCAAGAAA | 19016 |
rs217081128 | in-del | -/CTA | | | intron-variant | Pparg | Mm_Celera | 6:115389069 | CAAGGCCATCTTGAG[-/CTA]CATAGGGAGATGATG | 19016 |
rs217126096 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115435905 | ACTCCTGAGAATGGT[G/T]GTTGTTCACGCAAAT | 19016 |
rs217161675 | snp | A/G | | | upstream-variant-2KB | Pparg | Mm_Celera | 6:115359323 | AAACTGACACAAGGG[A/G]TGGGCTGGCCTTAGG | 19016 |
rs217188130 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115385304 | GGGAACCATCGCCCA[C/T]CTAAAGGAAAGCAAG | 19016 |
rs217194419 | in-del | -/TT | | | intron-variant | Pparg | Mm_Celera | 6:115372263 | TTATAGCTCTTGACC[-/TT]TTTTTTTTTTTTTTA | 19016 |
rs217208933 | in-del | -/TTACC | | | intron-variant | Pparg | Mm_Celera | 6:115397687 | TTCCGACTTGTAGTT[-/TTACC]TTGAAGCCCTCAAGA | 19016 |
rs217216035 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115460470 | TACCTCTATGTTATT[G/T]TCTTCATCATCCTTC | 19016 |
rs217222120 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115435217 | ATAAATTTGATTTTG[C/T]TTACTTTTTTTTTTC | 19016 |
rs217231753 | in-del | -/G | | | intron-variant | Pparg | Mm_Celera | 6:115428179 | CAGTCAAATGAGGGT[-/G]GAAACCCCCTGACAC | 19016 |
rs217258798 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115473502 | AGAGTGAAGGTGGTG[A/G]GGATCCCAGGTTCCT | 19016 |
rs217276136 | in-del | -/AAAGATAACTTTTT | | | intron-variant | Pparg | Mm_Celera | 6:115446446 | CACAGTTTATGGTCA[-/AAAGATAACTTTTT]AAAATTTTAATATTT | 19016 |
rs217280592 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115470651 | AATCATCTTCATCCA[C/T]TCATAGTTCTCTCAA | 19016 |
rs217324852 | in-del | -/T | | | intron-variant | Pparg | Mm_Celera | 6:115472735 | AGAGCCTCTCTCCTG[-/T]TTTAAGTGCCTTCAT | 19016 |
rs217340633 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115425444 | TGAGCTTCCTCTCCA[C/G]CCTTGGTTGTGTTGC | 19016 |
rs217347570 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115391593 | CCAACATGGAAAGAC[A/G]GGAGATGTTGGAGGT | 19016 |
rs217356372 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115482210 | AACATGTGCACAATG[A/C]GTCCTGCAGCAGGCA | 19016 |
rs217385393 | snp | A/G | | | upstream-variant-2KB | Pparg | Mm_Celera | 6:115359145 | CCAATGAGAATGAGG[A/G]GGATGAGGAGGAAGT | 19016 |
rs217402978 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115481053 | AAAATTCCACCAACC[A/G]TCCTTAAAATCCTTC | 19016 |
rs217436277 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115390894 | AGCCAATCTTGAAAA[A/C]AGTAGGATTTTCATG | 19016 |
rs217436426 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115399962 | TCTTCTGGCCTCTGG[A/G]GGCATTGCTCACATG | 19016 |
rs217447546 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115454821 | TATGTTGATTTGGCC[C/T]TGTTGCCTGCAGTGA | 19016 |
rs217510125 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115433599 | AAAGTGGAGGATGAA[A/G]TAGGGCTGGGCTAAA | 19016 |
rs217513605 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115389721 | TTCCATGGGACTAAA[A/G]GGAAACAGCAGTGAC | 19016 |
rs217514554 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115426046 | ATATCCCTGCCCCAC[A/C]CAATTGTGAATTAAA | 19016 |
rs217516415 | in-del | -/A | | | intron-variant | Pparg | Mm_Celera | 6:115392671 | AATGTAAAATACCTT[-/A]AAAAAAAGAACACAG | 19016 |
rs217539637 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115432466 | ATTCAACCCTTTTAC[C/T]ACCTCGTTCTTTCTC | 19016 |
rs217607018 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115435751 | AAAGCCAAGTTTGAA[A/G]GTCAAAAAGAAACAG | 19016 |
rs217611997 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115467161 | AACATTTCTGTACCC[A/T]CTTACATTTATGCTT | 19016 |
rs217615630 | in-del | -/T | | | intron-variant | Pparg | Mm_Celera | 6:115398225 | TTTTGCCTATCCCAA[-/T]TATTTCATATCAGTA | 19016 |
rs217731310 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115474890 | TGGGAATGGAACCGA[A/G]AGCCAGGCAAGCACC | 19016 |
rs217732522 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115378230 | GAGGCAGAGGCAGGT[C/G]GATTTCTGAGTTCGA | 19016 |
rs217735656 | in-del | -/TT | | | intron-variant | Pparg | Mm_Celera | 6:115409597 | AATTAACTAAAACAC[-/TT]TTTTTTTTCTTTCCC | 19016 |
rs217768841 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115453622 | GAGATTAAAGGCATG[C/T]GCTACCACTTCCAGA | 19016 |
rs217783867 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115474396 | GGTGCATGGTAATTA[G/T]TAAGGTCACTAAAAA | 19016 |
rs217811764 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115465364 | ACAGCACCCAAATCA[C/G]TAGAAATCACTTGGA | 19016 |
rs217854189 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115386778 | CTGAAAAAGTTCTGG[C/T]GATGGCTGCTCACCA | 19016 |
rs217927701 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115394506 | CCAAGAAAGATGTGA[A/G]TACACAGTACGGAAG | 19016 |
rs217927998 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115386074 | GTGCTACTCAGCACC[C/G]GTAGCTGGGGGTAGG | 19016 |
rs217934402 | snp | C/T | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115420116 | GACAAGTTCCAATTC[C/T]AGCCTCGCCTAATCT | 19016 |
rs217962712 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115427960 | AATAGCCTTTTCCAC[C/T]CTTTCTCCTCTTCTG | 19016 |
rs217992065 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115431065 | TTAACATTATTAAAC[A/G]GTGATTAATTATACA | 19016 |
rs217993365 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115437824 | ACAGACCTTCAACAA[A/G]TCATAAATCCTCACT | 19016 |
rs218014859 | in-del | -/AAAG | | | intron-variant | Pparg | Mm_Celera | 6:115432287 | TTAGTAAAAAAAAAA[-/AAAG]GTAGCGCCTCAGTGT | 19016 |
rs218032360 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115370388 | gtcaaatagagcttc[A/G]aaaacagtttccggg | 19016 |
rs218064436 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115436710 | GAAATTATGTCAGTA[C/T]TAAAGAGGAAGATTC | 19016 |
rs218074708 | in-del | -/CTT | | | intron-variant | Pparg | Mm_Celera | 6:115404221 | CCTCGCCATACTTTA[-/CTT]CTTCTTTCCAAACAT | 19016 |
rs218093307 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115419334 | CAGAGGCAGGTGGAT[G/T]TCTGAGTTCGAGGCC | 19016 |
rs218159683 | snp | A/G | | | intron-variant, upstream-variant-2KB | Pparg | Mm_Celera | 6:115362100 | CCCTGCCCGGGGCTC[A/G]CCAGGTGTGAGGAAA | 19016 |
rs218189798 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115393025 | CAGAGGACACTTTTG[C/T]GCAGTTGGCTCTCTC | 19016 |
rs218193845 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115430323 | TTTTTATTGTCCCTG[A/G]AGCATATGATTGTGT | 19016 |
rs218227873 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115376564 | GTATATCAGACATCT[C/G]AAGTAAAAAATTCAT | 19016 |
rs218265652 | snp | C/G | | | intron-variant | Pparg | Mm_Celera | 6:115392218 | CTTGACTGGACTGGA[C/G]CAACTATATCCTGTC | 19016 |
rs218300292 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115400733 | TAGGAGTGAGGAGGC[A/T]GAGAAGGGGCTGAAT | 19016 |
rs218363234 | snp | C/T | | | intron-variant, downstream-variant-500B | Pparg | Mm_Celera | 6:115463668 | TGTGTCCCACTTCTA[C/T]CTTTCAGTTTTTCTA | 19016 |
rs218375679 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115375073 | CTGCCACAAGGGCAG[A/G]AAATGCTTTGTCATT | 19016 |
rs218417104 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115431766 | ACATATTTATAATCC[C/T]AGTACTGGGCAGGGG | 19016 |
rs218424044 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115387538 | GGGCTTTCCAGACTC[A/T]TAAGTCTACACAGAG | 19016 |
rs218437113 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115472602 | GAGTGAGTTCCAGGA[C/T]AGCCAGGGCTACACA | 19016 |
rs218448201 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115471262 | GTCAGCTTCCCAACA[A/T]TAATAGTGCGGGCTT | 19016 |
rs218494733 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115378407 | AAGATAAGCTAGTTA[C/T]TGAGAGTTAGTATTA | 19016 |
rs218506280 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115482616 | TTACCATTCTAGCTC[C/T]GCTTAAAACCATTGT | 19016 |
rs218518318 | in-del | -/AG | | | intron-variant | Pparg | Mm_Celera | 6:115489541 | GGTAGAAGTTTAAAA[-/AG]GAAAACAAAATAAAA | 19016 |
rs218528224 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115377425 | TTGAAGGAAGCCAGG[A/G]CAGGAGCTCAAACAG | 19016 |
rs218529303 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115475818 | ACATACGCATGCATA[C/T]ACACAAATATACATG | 19016 |
rs218538138 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115389118 | TTGTCAATGAAAAAA[G/T]TATTATTGGGGACTG | 19016 |
rs218757041 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115465634 | TTATGCCCTTTGAAA[C/T]CATGGACTTTCAACA | 19016 |
rs218770413 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115480454 | ACAGTGTTGTCTGAG[A/G]CAGACAGGACTGAAA | 19016 |
rs218805409 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115372528 | AACATCAGAAGAAAA[G/T]TTTATTCTGCTCACC | 19016 |
rs218837364 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115446787 | AATCCCAAAACTGAT[A/G]AACGAGAGAAACTCA | 19016 |
rs218853165 | snp | A/T | | | utr-variant-5-prime | Pparg | Mm_Celera | 6:115383721 | ATTCAGGACATTTTT[A/T]AAAACAAGACTACCC | 19016 |
rs218862942 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115477610 | AAAGCTCTTGTTAAT[G/T]CAGAGAAGCTTGGAA | 19016 |
rs218888692 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115459264 | GGTACAAAAATATAT[A/G]TGCAAGCAAAATATT | 19016 |
rs218963298 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115476788 | TTTGCTGGGTAAATA[A/G]GTGTTACTACCCACT | 19016 |
rs219033852 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115418359 | CTGGTCCTTTTCTTG[A/G]CTCTAAATTCACCCT | 19016 |
rs219041957 | in-del | -/TGTGTGTGTGTG | | | intron-variant | Pparg | Mm_Celera | 6:115375359 | GTTTCACAATTAGAT[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 19016 |
rs219069923 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115458116 | GCTATAGAAAGCACA[G/T]CCTCTGCACTGCTTC | 19016 |
rs219071749 | snp | G/T | | | intron-variant | Pparg | Mm_Celera | 6:115429822 | ATTAAGATAATTCTG[G/T]CCTCATAGCATCAAG | 19016 |
rs219095936 | in-del | -/T | | | intron-variant | Pparg | Mm_Celera | 6:115422623 | ACTTTGAAATCTACA[-/T]TTTTTTCCCAAAGAA | 19016 |
rs219131729 | in-del | -/AT | | | intron-variant | Pparg | Mm_Celera | 6:115486289 | TACATAGGCATATAC[-/AT]ATATACACATAGCCA | 19016 |
rs219138181 | in-del | -/GG | | | intron-variant | Pparg | Mm_Celera | 6:115386201 | AACAAGAATTGCAAC[-/GG]TTTTTTGTGTGTTTT | 19016 |
rs219144604 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115429124 | TCAGATGCTGGTTTT[A/G]TTTGTTTTGGGTTTG | 19016 |
rs219161876 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115412319 | GTTGGTAAATGGTTT[A/G]TGTGTGTGTGATAAA | 19016 |
rs219167457 | in-del | -/A | | | intron-variant | Pparg | Mm_Celera | 6:115447057 | TGTTTACCTGTTTTT[-/A]AAAAATCACTGAAAA | 19016 |
rs219176843 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115439077 | ATTAGCAGCCCTACC[A/G]CTAGAAATATGGCCA | 19016 |
rs219182292 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115432048 | TCTTTTCTACTTTTC[C/T]ATATTATTACCTGAT | 19016 |
rs219266014 | snp | A/T | | | intron-variant | Pparg | Mm_Celera | 6:115414488 | GTTTAAAAATGTAAA[A/T]TCTATAAATGAAGCA | 19016 |
rs219284985 | in-del | -/C | | | intron-variant | Pparg | Mm_Celera | 6:115461565 | AAATGTTCCTGTATA[-/C]CTTGTCTTATGATAA | 19016 |
rs219292558 | in-del | -/CTT | | | intron-variant | Pparg | Mm_Celera | 6:115372299 | CTATGCAATGTATAC[-/CTT]CCTTAGTTCCGGCCT | 19016 |
rs219312375 | in-del | -/G | | | intron-variant | Pparg | Mm_Celera | 6:115372182 | TACTTTTGCTGATTT[-/G]GGGGGGGTGTCATTT | 19016 |
rs219319027 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115471348 | CCGGTCTACAGAATG[A/G]ATTCCAGGACAGCCA | 19016 |
rs219386530 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115426629 | TGCTCGTGCAACTAA[C/T]AGCAGCTGCAGCCCC | 19016 |
rs219411594 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115458211 | CATGCAGCTAGGATT[A/C]CCTGGGACTCCAAAT | 19016 |
rs219413437 | snp | A/C | | | intron-variant | Pparg | Mm_Celera | 6:115411155 | CCTTGTCTGTGTCAT[A/C]TGTAAATGAAGCACT | 19016 |
rs219417502 | snp | A/G | | | intron-variant | Pparg | Mm_Celera | 6:115425608 | CTCAGGGTCAGGGTG[A/G]GGAAGCTTTTCTAGG | 19016 |
rs219443780 | snp | C/T | | | intron-variant | Pparg | Mm_Celera | 6:115457354 | ATTTGCCTTTTTATT[C/T]TGTAAAGCCTCAAAT | 19016 |