SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3022739 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35526978 | TGAAGTAATTCTCAA[G/T]AAACCCCTCTACTAT | 11622 |
rs3022740 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535501 | AATAAAACATCGTTT[C/T]CTCCATCAGACTTCA | 11622 |
rs3022741 | snp | C/G | 0.152778 | 0.230321 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535510 | TCGTTTCCTCCATCA[C/G]ACTTCAGGAAGATGA | 11622 |
rs3022742 | snp | C/G | 0.152778 | 0.230321 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535593 | CTGAGACTATGACCA[C/G]AGACCTGAGTTTCTG | 11622 |
rs3022743 | in-del | -/A | 0.486111 | 0.0821678 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535639 | AGCTGNTGGGAGNNN[-/A]AAAAAAAAAAAAAGA | 11622 |
rs3022744 | in-del | -/A | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535640 | GCTGATGGGAGGAAA[-/A]AGAAAAAAAAAAAAA | 11622 |
rs3022745 | in-del | -/A | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535641 | CTGATGGGAGGAAAA[-/A]GAAAAAAAAAAAAAG | 11622 |
rs3022747 | snp | A/T | 0.244898 | 0.249948 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535679 | CTAGGAACAAATCAT[A/T]AAGATTTAATGAAGA | 11622 |
rs3022748 | snp | A/C | 0.277778 | 0.248452 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535692 | ATAAAGATTTAATGA[A/C]GAAATTGGGTCTCAT | 11622 |
rs3022749 | snp | A/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535746 | AAAGGCGTAATTTGG[A/G]AGATGATGTTCCATC | 11622 |
rs3022750 | snp | G/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536024 | GATAGAGATGAAGTC[G/T]GATGTGTTTTATAGA | 11622 |
rs3667105 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ahr | Mm_Celera | 12:35531782 | CATTCCTGAATACTA[A/G]CAAGGTAAAAATTGA | 11622 |
rs3667122 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ahr | Mm_Celera | 12:35531793 | ACTAACAAGGTAAAA[A/G]TTGATATTGGTGTGT | 11622 |
rs3667190 | snp | A/G | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35531840 | TGAGAGCCTTGCTAC[A/G]GCTGGCTTGAATACC | 11622 |
rs3667618 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Ahr | Mm_Celera | 12:35531845 | GCCTTGCTACGGCTG[C/G]CTTGAATACCACCAC | 11622 |
rs3668383 | snp | A/G | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35532014 | TCTTCTGCTTTGCTC[A/G]GCCATTTTCATGAGA | 11622 |
rs3668390 | snp | C/T | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35532020 | GCTTTGCTCAGCCAT[C/T]TTCATGAGACTGAAT | 11622 |
rs3680691 | snp | A/G | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35522154 | AATTATTAGCTGACC[A/G]TGGTAGTGAACACCT | 11622 |
rs3680718 | snp | C/T | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35522165 | GACCGTGGTAGTGAA[C/T]ACCTCTAATCCTAGC | 11622 |
rs3680739 | snp | C/T | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35522177 | GAACACCTCTAATCC[C/T]AGCACTCAAAAGGCA | 11622 |
rs3692249 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Ahr | Mm_Celera | 12:35525518 | TCCCTGGCACAGTTA[A/G]AGTCAAGGAGCTGGC | 11622 |
rs3692772 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Ahr | Mm_Celera | 12:35525560 | TGGAGAATGAAACCC[A/G]ACACTGTTGATTCCA | 11622 |
rs3695108 | snp | G/T | 0.301783 | 0.244578 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535469 | CCTCCCACATTTATT[G/T]TATGTCTACAGAAGA | 11622 |
rs3695709 | snp | A/G | 0.301783 | 0.244578 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535556 | AGGAGTGCTGAGAGC[A/G]TGAGAAATTGGAGGG | 11622 |
rs8237542 | snp | A/C | 0.252401 | 0.249988 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535168 | ACACTTCTTGCAGTC[A/C]GAGGTTCTGGGGGTG | 11622 |
rs8237543 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535182 | CCGAGGTTCTGGGGG[C/T]GGGGTGGTGTTCGCC | 11622 |
rs8237544 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535293 | TTTACCAGGCAAAGA[A/G]CTTAGCTCATCCTAG | 11622 |
rs8237545 | snp | C/T | 0.336735 | 0.234472 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535296 | ACCAGGCAAAGAGCT[C/T]AGCTCATCCTAGAGT | 11622 |
rs8254591 | snp | G/T | 0.152778 | 0.230321 | missense | Ahr | Mm_Celera | 12:35504093 | GTAAGCTGGAAAAGA[G/T]CTGATAGTGCTTTAG | 11622 |
rs8254592 | in-del | -/G | 0.142012 | 0.225474 | frameshift-variant | Ahr | Mm_Celera | 12:35504254 | TCCAGAGCCTGCGGC[-/G]GGGGCTGCTGAAGCT | 11622 |
rs8254593 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35500506 | GTGTACTGATGTCCA[A/C]CNCTCACAGTTCTGG | 11622 |
rs8254594 | in-del | -/A | 0.197531 | 0.244432 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35500193 | AAACCATTTACTTTA[-/A]CTTCTGGGACAAAAA | 11622 |
rs8254614 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499962 | CACAGCGGGGTCATA[A/G]AAAGGTTGGGATTCG | 11622 |
rs8254615 | snp | A/G | 0.304688 | 0.243945 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35500143 | ATTAACAGTGCAGAA[A/G]GAAAGCATTGAGATT | 11622 |
rs8254617 | in-del | -/A | 0.124444 | 0.216185 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535263 | GGCAAATTCCTTGTA[-/A]CCCAGACATCAAGAT | 11622 |
rs8254618 | in-del | -/T | 0.18 | 0.24 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535312 | AGCTCATCCTAGAGT[-/T]GAGTCATCTAATTTT | 11622 |
rs8254619 | snp | C/G | 0.152778 | 0.230321 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535329 | AGTCATCTAATTTTT[C/G]ACAAAGATTTTACAT | 11622 |
rs8254620 | in-del | -/T | 0.459184 | 0.136902 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535946 | GCCTCTATTCTTTGG[-/T]GGTTAANAGCGACCT | 11622 |
rs8254621 | snp | C/G | 0.244898 | 0.249948 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535905 | TTTATCATCTCTGCT[C/G]TCTCNTTTCTCTCAT | 11622 |
rs8254622 | snp | C/T | 0.260355 | 0.249785 | upstream-variant-2KB | Ahr | GRCm38.p3 | 12:35535900 | CATCTCTGCTNTCTC[C/T]TTTCTCTCATCCCCA | 11622 |
rs8254623 | snp | A/C | 0.260355 | 0.249785 | upstream-variant-2KB | Ahr | GRCm38.p3 | 12:35535737 | TCATCTTCCAAATTA[A/C]GCCTTTAAAAGCTCT | 11622 |
rs8254637 | in-del | -/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535693 | TNAANATTTATTGAN[-/G]AAATTGGGTCTCNTT | 11622 |
rs8254638 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Ahr | GRCm38.p3 | 12:35535429 | TATAAAACTCGTAGC[C/T]TTCAAGACAACTAAC | 11622 |
rs8254639 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB | Ahr | GRCm38.p3 | 12:35535427 | TAAAACTCGTAGCCT[C/T]CAAGACAACTAACTT | 11622 |
rs8254640 | in-del | -/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535262 | TCTTGATGTCTGGGT[-/T]ACAAGGAATTTGCCT | 11622 |
rs8254641 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535382 | CGACTGGAGAGCATT[C/T]TANGNAGAAAACTTC | 11622 |
rs8254649 | in-del | -/T | 0.152778 | 0.230321 | intron-variant | Ahr | Mm_Celera | 12:35515172 | CACAAAAGGCACATA[-/T]TCAAACAAGCACTAT | 11622 |
rs8254650 | in-del | -/T | 0.132653 | 0.220748 | intron-variant | Ahr | Mm_Celera | 12:35511207 | AAAAACTTATAGTGA[-/T]TTGAAGAGTGATAAG | 11622 |
rs8254651 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Ahr | Mm_Celera | 12:35509935 | TCTTTTATTATATTA[A/C]GTCATGATATTTTAA | 11622 |
rs8254656 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ahr | Mm_Celera | 12:35510146 | TGCTGTGAAATCAAG[A/G]GTGACAGTGGTGACA | 11622 |
rs8254657 | in-del | -/T | 0.142012 | 0.225474 | intron-variant | Ahr | Mm_Celera | 12:35510167 | AGTGGTGACAGACTT[-/T]AAACNNNNNNCTGTA | 11622 |
rs8254658 | in-del | -/A/G/T/TAGAGT | 0.737673 | 0.0462566 | intron-variant | Ahr | Mm_Celera | 12:35510171 | TGACAGACTTNAAAC[-/A/G/T/TAGAGT]NNNNNCTGTATNTTG | 11622 |
rs8254665 | snp | C/T | 0.18 | 0.24 | intron-variant | Ahr | Mm_Celera | 12:35510199 | TTAAAAATACCATTT[C/T]GAAAATAATTGAAAA | 11622 |
rs8254667 | in-del | -/A | 0.444444 | 0.157135 | intron-variant | Ahr | Mm_Celera | 12:35508115 | GAAGAATTANGAGTG[-/A]AAANGTTCCCTTACT | 11622 |
rs8254668 | in-del | -/A | 0.375 | 0.216506 | intron-variant | Ahr | GRCm38.p3 | 12:35508336 | GAAATTCATTGCCTT[-/A]AAAAAAATATGTCAT | 11622 |
rs8254669 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ahr | Mm_Celera | 12:35507276 | GGTTGATCCTAGGGA[C/T]GCACAAAGGCAAAGA | 11622 |
rs8254670 | in-del | -/A | 0.32 | 0.24 | intron-variant | Ahr | Mm_Celera | 12:35506182 | TAGGATTCTTTTTCA[-/A]CTTTCNTGTAAGAAG | 11622 |
rs8254673 | snp | A/C/T | 0.31405 | 0.280505 | intron-variant | Ahr | Mm_Celera | 12:35506460 | tacantacagtacan[A/C/T]ncTGCANNTAAGTGG | 11622 |
rs8254676 | snp | A/T | 0.32 | 0.24 | intron-variant | Ahr | Mm_Celera | 12:35505381 | ACATTCACTATGGTT[A/T]TGGGTTAATGACTCA | 11622 |
rs8254677 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ahr | Mm_Celera | 12:35505396 | ATGGGTTAATGACTC[A/G]GTTCTGTGCAAATGT | 11622 |
rs8254678 | snp | A/G | 0.32 | 0.24 | intron-variant | Ahr | Mm_Celera | 12:35505492 | GGGGATTTAGTCTTT[A/G]ATAAATGAGTTTTAA | 11622 |
rs8254679 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ahr | Mm_Celera | 12:35505504 | TTTAATAAATGAGTT[C/T]TAAAGTACATTTGGA | 11622 |
rs8254680 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ahr | Mm_Celera | 12:35505558 | AAGACAATTATGAAC[G/T]AGAACAAAATGTATC | 11622 |
rs16794373 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535748 | AGGCTTAATTTGGNA[A/G]ATGATGTNCCTTCTT | 11622 |
rs29132148 | snp | C/T | 0.32 | 0.24 | intron-variant | Ahr | Mm_Celera | 12:35508540 | AAGTGACCTACCCTG[C/T]CCCCAAGTCATGACA | 11622 |
rs29146187 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Ahr | Mm_Celera | 12:35519434 | CCGCTGAAGCAATCC[C/T]ATAGTGGAAAGAACT | 11622 |
rs29149867 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ahr | Mm_Celera | 12:35513510 | TATTTCTATTCGTTT[A/G]AGCCACACTCTACCC | 11622 |
rs29176532 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ahr | GRCm38.p3 | 12:35503319 | ATTTAAGCCACACTT[G/T]TAAATGGCTATACTC | 11622 |
rs29184676 | snp | A/G | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35533134 | TCAAGCGGAGCTCCA[A/G]GTTTTATGCCCATGT | 11622 |
rs29196351 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ahr | Mm_Celera | 12:35508857 | TTAGACATGGGTGTC[A/G]TAAACTCAGCTGATC | 11622 |
rs29198961 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499646 | CCTCACTGCAGCGTA[A/G]TGGACATAGGCACCT | 11622 |
rs29210568 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Ahr | Mm_Celera | 12:35508681 | GTCAAACTACATATT[A/C]ATTTTCAAACATGTA | 11622 |
rs33847342 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Ahr | GRCm38.p3 | 12:35532764 | AGCACTAAAGTCTTC[A/C/G]ACAAAGCAAGCTGGT | 11622 |
rs45652484 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35516798 | TGAGTCCAGAAATAG[G/T]ATGTGCTCTCCATTC | 11622 |
rs45654728 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533793 | CTCAATCATGAATCT[C/T]TTTTCTGAGGGGGGA | 11622 |
rs45691767 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35533588 | GGTTTTTTTGTTGTT[G/T]TTGTTTTCTTTTTTT | 11622 |
rs45720212 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35531968 | CTTCAAAATATATTT[A/C]AAGTTTTAATCACCA | 11622 |
rs45812769 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35513920 | CAAGCCTGGAACCCA[A/G]CAGGGCAAACGCCAG | 11622 |
rs45879619 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525392 | AGGAATTCCATTTTG[A/G]AATTACTGTGGTGAT | 11622 |
rs45904323 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35514016 | TTGGGCATTTGAACA[C/G]TTGGTCTCAATTTGG | 11622 |
rs45915597 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35523504 | TGGTGAGGAATAATA[C/T]AAATAAGTAGTAAAC | 11622 |
rs45931008 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35530371 | TACAGACCTCCAGAC[G/T]ATTCTCTGAAACACC | 11622 |
rs45942625 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35520720 | ATGACACACTCCATG[C/G]GTCACACCAATAATC | 11622 |
rs45949636 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533322 | TAAAGCACTGAAAGC[C/T]AGGGTCCAAAGAACT | 11622 |
rs45965099 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35522701 | AGATCGATTCATGCC[A/G]TATTATTTGAACTTG | 11622 |
rs45978460 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35519282 | ATTCTGCTACCTGAG[A/T]AGCATCTGTTAAGCG | 11622 |
rs45984672 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35525203 | CACATGCCTTAATAA[A/C]TCAATTTTTTATGAA | 11622 |
rs46000574 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35527045 | CTATGAAATAACTAT[C/G]AGATAATACCAAACA | 11622 |
rs46004999 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35521283 | ACATGAGAACAACTG[C/T]AATTATAGAATCCAT | 11622 |
rs46031753 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35518908 | TTTTCTTGCCTCTAC[A/G]TAAGAGGAATGCTGT | 11622 |
rs46054873 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529213 | GTCCTGTTGGCTTTC[A/G]TCAAGGAGAGATTTA | 11622 |
rs46129620 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ahr | Mm_Celera | 12:35530267 | GACTGTAACATTCGG[C/T]TCATCCTTAGAAGTA | 11622 |
rs46132423 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35532803 | AGGCATTTGAAGGCT[C/T]AGAGTTGATTAAAGG | 11622 |
rs46167218 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Ahr | Mm_Celera | 12:35517058 | TCCTACCTTTAGAAT[G/T]TCTCTACTCACTCGG | 11622 |
rs46170080 | snp | A/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536907 | ACCTGTGAGGTAGAA[A/G]CTGGAACTGTGATCG | 11622 |
rs46172663 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35531102 | TCCGGCAGTGTCTGT[A/C]TGTCAGGCCTGCAAC | 11622 |
rs46187218 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529366 | TATTTCTTAAGCAGA[A/G]GCATGTTCTTTTTTT | 11622 |
rs46220021 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35530362 | ATAAGAGTTTACAGA[C/T]CTCCAGACGATTCTC | 11622 |
rs46252848 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533131 | CACTCAAGCGGAGCT[C/T]CAAGTTTTATGCCCA | 11622 |
rs46267352 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35518939 | CACTTGAGATGAATT[A/G]TGGTGAGTATAAAAT | 11622 |
rs46296806 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35521105 | CTCCACTAAGAGCTC[A/G]TATGAGCTCGTTAGC | 11622 |
rs46317989 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35531021 | TGCGTAGTGCTCACT[C/T]CTAAGTAATGGTGTT | 11622 |
rs46346037 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35534427 | GCCAGGGAAGGTCGC[C/T]GAGCAGTAAAGGTGC | 11622 |
rs46422371 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Ahr | Mm_Celera | 12:35532832 | GGTGTTCAGTACAGA[G/T]CTGATAAACAGAAGT | 11622 |
rs46424239 | snp | A/G | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35532412 | TCGGGTTAAAATCAT[A/G]TCACCCACTTTACTC | 11622 |
rs46446783 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35527664 | GGAGATAGCCAAGAA[C/T]GGACACACCCACAAG | 11622 |
rs46483026 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35520264 | CCTCCTCTGCTGCCC[C/T]GAAGTGTGTTTCTTG | 11622 |
rs46485439 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35502387 | AAAGGTTGTAGAAAA[A/G]AAAGGGAAACAGAAA | 11622 |
rs46487535 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35515706 | TTATTAGATTTCTAT[A/G]TTCCCCTGGTTCAGG | 11622 |
rs46495352 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35530664 | CCAGGACAGGGGCCA[C/T]CATGCACTCTGATTA | 11622 |
rs46501177 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35519421 | CTTCCTCTGAAGGCC[A/G]CTGAAGCAATCCCAT | 11622 |
rs46516328 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35521430 | TCAGATTGGCATACC[A/G]GGAGGTGGGCCTTAC | 11622 |
rs46552607 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35531886 | TTTATTGATTGAGCA[C/T]CTGCTGTTTGCTAGC | 11622 |
rs46578638 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ahr | Mm_Celera | 12:35507096 | GCTGTAGAGGAATTA[G/T]AAGTAAAAAGCAAAA | 11622 |
rs46612549 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35514627 | GCTGGGGGAAAAAAA[A/C]CTATAACATGTAAGT | 11622 |
rs46623572 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ahr | Mm_Celera | 12:35523628 | ACATGTCCATCATGC[A/T]TGTGTGTGAACCTAC | 11622 |
rs46639856 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35532541 | AAGTTAATTAAATTA[A/G]AAAGCACAGTCAACA | 11622 |
rs46643565 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35521590 | CTTTGGACTTTTAAA[C/T]AGACTTTTGAGATTG | 11622 |
rs46652935 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ahr | Mm_Celera | 12:35529956 | CACACTGTGGGCAAG[A/G]TGGCAGGTACTGTGT | 11622 |
rs46655524 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35520731 | CATGGGTCACACCAA[C/T]AATCCCAGGCAACTC | 11622 |
rs46669206 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahr | Mm_Celera | 12:35516670 | AGCACTTGACATGCA[C/T]GATAAATGGGTTCCT | 11622 |
rs46688281 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35521921 | CGGTCTTCTCCATCA[C/T]AGCTCACCCTCTGAA | 11622 |
rs46785540 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35514394 | CTCCCCTCACTTCAC[C/T]GGCCAGAGCTGCAGG | 11622 |
rs46790967 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35520608 | GACTAATACATTATA[C/T]CAGTTACTATGAAAC | 11622 |
rs46795851 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ahr | Mm_Celera | 12:35525156 | TTAATCCATTCACTA[C/T]AATTCGTGAAAGAAT | 11622 |
rs46811011 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35519031 | CCCTGGAAGCACTAC[A/T]AAAAACCTCATAAAC | 11622 |
rs46856064 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Ahr | Mm_Celera | 12:35525457 | CTGAACCATGCAGGC[A/C]GCACTGCCACCCTCA | 11622 |
rs46865339 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35516321 | TCTCTTCACATTAAT[C/T]TTTGGATGATGGAAT | 11622 |
rs46901269 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ahr | Mm_Celera | 12:35516016 | TCACTGAAATGCAGA[A/G]CAGAGAATGGCCTTT | 11622 |
rs46902408 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35514771 | ACATTGTTTTGAAAG[C/T]GCACACAGATTCATC | 11622 |
rs46909984 | snp | G/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536692 | TGGGAGCATGGTAAT[G/T]CATACATTTCATTAA | 11622 |
rs46923435 | snp | C/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536772 | TGATAGTTTTCTCAA[C/T]TATGTTTCCAGCTGG | 11622 |
rs47003104 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35523963 | ATCTGGTGCAGCAGG[A/G]ATCACAACCTATGAG | 11622 |
rs47014845 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35523491 | AGCATGATGTAATTG[A/G]TGAGGAATAATACAA | 11622 |
rs47046527 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35530440 | CCTCGAAAGGAAAAT[A/C]CTGGAGTTAGTCAAC | 11622 |
rs47070167 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Ahr | Mm_Celera | 12:35524904 | CTTGTTAAGAAAATA[C/T]ACAACTGTGCAAGCA | 11622 |
rs47084969 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ahr | Mm_Celera | 12:35525109 | GTGATGCCTAGTGAC[A/G]TATAAGCACACAACA | 11622 |
rs47093592 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35530136 | ATACCAGCTCAACCA[C/T]TCCCATCACTTGGTA | 11622 |
rs47116103 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35516054 | TTCTGTACATTCTTA[C/G]CTAGTGTTGCTGCTT | 11622 |
rs47149924 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Ahr | Mm_Celera | 12:35529543 | CAGTGATGTAGGTGG[A/T]TTAGCAAGTGTTCCT | 11622 |
rs47198379 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35524509 | CAGACCATATGGAAT[C/G]ACCACTGTAGGAGTT | 11622 |
rs47238033 | snp | A/G | 0.124444 | 0.216185 | missense | Ahr | Mm_Celera | 12:35507431 | TCACTGCGGATGTGG[A/G]ATTCTGCACAGTGAA | 11622 |
rs47242658 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Ahr | Mm_Celera | 12:35531962 | ATAAAGCTTCAAAAT[A/T]TATTTCAAGTTTTAA | 11622 |
rs47280811 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ahr | Mm_Celera | 12:35516502 | CTTTCAGGAGGATTT[G/T]CAAGCTCTAGAAATA | 11622 |
rs47288889 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35521794 | CCTTATTGAAGTAGC[A/G]GTGTCACTAAAAGTG | 11622 |
rs47318212 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35523893 | GCCTGAAGCCCCTGT[A/G]CATGAAATTCTCTAA | 11622 |
rs47330723 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533345 | AAAGAACTGCCGGGG[C/T]AGAAAACTGCTGAGT | 11622 |
rs47334451 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Ahr | Mm_Celera | 12:35532808 | TTTGAAGGCTCAGAG[A/T]TGATTAAAGGTGTTC | 11622 |
rs47387002 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35519807 | AGTTAAATTCCTTGA[C/T]AACACTGGTGTACAC | 11622 |
rs47439436 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35524424 | CTATGAAACTAAGCA[C/T]GATCCCACCACTGTA | 11622 |
rs47478110 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35516019 | CTGAAATGCAGAGCA[A/G]AGAATGGCCTTTTCT | 11622 |
rs47534328 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35519131 | AGATGACCAGATGGT[A/G]CCTAAAATAGTTCAA | 11622 |
rs47559383 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahr | Mm_Celera | 12:35519766 | TAACATTTATCACTT[C/T]CTATCATTAATTATT | 11622 |
rs47580897 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35531593 | AGAAAATGAAAAATA[C/G]TACGGTAGCTGCAAA | 11622 |
rs47591272 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35529834 | AAAAACAATGAAAGG[A/C]TGAAAGCATATTTAA | 11622 |
rs47592167 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35518972 | AATGCAGCTTACACA[C/G]GAGCAGTAAAGGCCA | 11622 |
rs47597010 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35519539 | CAACTGACAGTCACT[A/C]AATTTACGTTTTCTA | 11622 |
rs47601417 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ahr | Mm_Celera | 12:35527416 | TTTTATGACCTCAAT[A/G]CAGAACCACTGATAA | 11622 |
rs47623406 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35520098 | TTGTGTGTAAGTGTG[C/T]TTTTCCTGCATGTAT | 11622 |
rs47694388 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35524482 | ATCACTGTGGTCAGA[C/T]TCTGTACACTACAGA | 11622 |
rs47734431 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ahr | Mm_Celera | 12:35531088 | TGGGGAAAATAAGAT[C/T]CGGCAGTGTCTGTCT | 11622 |
rs47761788 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35530137 | TACCAGCTCAACCAT[C/T]CCCATCACTTGGTAA | 11622 |
rs47765745 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ahr | Mm_Celera | 12:35529679 | GCAGAAATCCTGTCT[C/T]TCACACACCTAAGAC | 11622 |
rs47804136 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35508605 | TGACATTTCCACCTT[C/T]TACAACCCTTTGCAC | 11622 |
rs47821194 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35519869 | CATAAACATATATAT[A/G]TGTGTGTGTGTATAA | 11622 |
rs47831308 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35521256 | GTATTCTATAGGACA[G/T]ATGAGTAACTCACAT | 11622 |
rs47876272 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35516523 | TCTAGAAATAAAGTG[C/G]TAGAAGAGAATGTCA | 11622 |
rs47927535 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35516568 | CTCAGGGCAGGTTTA[A/G]AAGGCATTTCGGAAA | 11622 |
rs47949668 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35532230 | TTCATTGCACTGAAG[A/G]AGGAGGAAACAGCTA | 11622 |
rs47975772 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35519212 | ATGGAAACTTAACAG[C/T]CCTGGACCATGTGAC | 11622 |
rs48059541 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35530018 | ACAGGAATTTAATTC[C/T]GAACAAGAGAAAGAA | 11622 |
rs48064959 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ahr | Mm_Celera | 12:35531730 | AGATGGGGCTCACAA[C/T]GTTTTAATAGAGTGA | 11622 |
rs48068291 | snp | C/G | 0.46281 | 0.131194 | intron-variant | Ahr | Mm_Celera | 12:35529490 | TTACCAGGACCAAAC[C/G]TATTCTATAGGGAGG | 11622 |
rs48087619 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35521352 | CCTCAGAACAGGCAC[A/G]CCTGGTTCACACAGA | 11622 |
rs48140298 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35521333 | AGCATTAAGCCACTT[C/T]AGACCTCAGAACAGG | 11622 |
rs48161813 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35531068 | GAGACTGTACTGGTC[A/T]CTGCTGGGGAAAATA | 11622 |
rs48194391 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35533346 | AAGAACTGCCGGGGT[A/G]GAAAACTGCTGAGTC | 11622 |
rs48241652 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35527120 | TACTAAAACCACTGA[A/G]CTGTCCAAAAAAAAA | 11622 |
rs48241855 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ahr | Mm_Celera | 12:35516856 | TGCTGTCTCGGAAAG[C/T]TTACATTATGCTCGC | 11622 |
rs48248293 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ahr | Mm_Celera | 12:35519359 | CAGGAATCTAAAAGT[C/T]GCCCAAGATAAGGAT | 11622 |
rs48266720 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35530463 | TAGTCAACAGAACAA[C/T]ATGCAGTTGTTCAAA | 11622 |
rs48288701 | snp | G/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536647 | GCAGCAGGAGTGGGG[G/T]AAGGAATGGGGGGGG | 11622 |
rs48318230 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ahr | Mm_Celera | 12:35530977 | AAACAGTTTTTAAAG[A/G]GTTTAGAAGTAGAAT | 11622 |
rs48336756 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ahr | Mm_Celera | 12:35529968 | AAGGTGGCAGGTACT[A/G]TGTGGCACTGACTTT | 11622 |
rs48359932 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35518985 | CAGGAGCAGTAAAGG[C/G]CAGACGTGATAAACT | 11622 |
rs48377214 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35530497 | CTTCACAGGGAGATG[A/T]GTGCAGGGAAATGGG | 11622 |
rs48384323 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35530295 | GTATATAAACCCTTG[C/T]CCCCCCAAATTCCAC | 11622 |
rs48451715 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ahr | Mm_Celera | 12:35529705 | AAGACACTGTACCCA[C/T]ATGAAAAAGACAATT | 11622 |
rs48490944 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ahr | Mm_Celera | 12:35521059 | GCCATTTCTAACAAG[A/G]GAAAATGTCATAGGC | 11622 |
rs48503506 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35523716 | GGTTATTCTAAGCAG[A/C]TTCAGGGCCATCCTC | 11622 |
rs48525810 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35519620 | ATTCATGAGGACAAA[A/C]TATGGGGTTCTGGTA | 11622 |
rs48544360 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Ahr | Mm_Celera | 12:35520745 | ATAATCCCAGGCAAC[A/T]CTACAAATCACACGC | 11622 |
rs48596698 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35519341 | TACCCCCTTCTAAAG[A/G]GACAGGAATCTAAAA | 11622 |
rs48608148 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ahr | Mm_Celera | 12:35532439 | ACTCCAAATTTTCAC[A/G]GAACTGTATATTTAA | 11622 |
rs48638622 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35519163 | CATCAAGAGGCACTT[C/T]ACACATCACGTATAT | 11622 |
rs48646735 | snp | A/T | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35507832 | AGACAGGGTCTGTCA[A/T]TTATTCTAAAAGGTG | 11622 |
rs48652893 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35526304 | ATTGGAGATTTGAAC[A/G]CAGATCTGCATTGTT | 11622 |
rs48666814 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35521633 | GGGACTTTTGAAGTT[A/G]CACTGAATGCACTTT | 11622 |
rs48693805 | snp | A/C/G/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35519303 | CTGTTAAGCGGTAAT[A/C/G/T]GACATCCGTGCAGTA | 11622 |
rs48781278 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35520440 | CTCCATATTATGCCT[G/T]TGGTCAGATGCAGTA | 11622 |
rs48802855 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35533265 | AACAAAGTCAAATTG[A/G]GCAAACATGTTTTAA | 11622 |
rs48804750 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35510257 | TGTAGAACTTGCCTC[C/T]TTCTATATTGGTAAT | 11622 |
rs48809140 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35520478 | GCATTAACACAACCA[G/T]AGTAGAAATGTCTGC | 11622 |
rs48828407 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Ahr | Mm_Celera | 12:35517072 | TGTCTCTACTCACTC[A/G]GTAATGACATATTGT | 11622 |
rs48852357 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ahr | Mm_Celera | 12:35529498 | ACCAAACCTATTCTA[C/T]AGGGAGGCAAGCAAG | 11622 |
rs48855519 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35532901 | AACAGTTTAGTTGTC[C/T]GAAATTATCAAATGC | 11622 |
rs48897837 | snp | C/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536915 | GGTAGAAACTGGAAC[C/T]GTGATCGAGAAGCTG | 11622 |
rs48897927 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ahr | Mm_Celera | 12:35525012 | GACACATTACAGATA[C/T]GAGGAGGTGCTGCCT | 11622 |
rs48935913 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35521159 | AGCATCACTTCCACA[C/G]ACGAGTTCATAGGTG | 11622 |
rs48956859 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531545 | CACATCCACAGCCTC[A/G]GCATAGATGCCCTCT | 11622 |
rs48980001 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35506971 | TTTAGTATTTCCCGA[C/T]TTTATATTAACATAT | 11622 |
rs49026643 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ahr | Mm_Celera | 12:35521506 | CACATGTCCTCTGCC[A/G]TGTACAGTCTCCATG | 11622 |
rs49028494 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ahr | Mm_Celera | 12:35508903 | CTATGTGACACACAT[C/T]TGATATAGCACAAGA | 11622 |
rs49030096 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35507847 | TTTATTCTAAAAGGT[A/G]GGAAAATTAAAATGC | 11622 |
rs49045849 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35523696 | GCTTGTATGGCAACG[C/T]GTATGGTTATTCTAA | 11622 |
rs49084102 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35515490 | AAGCTGTTGTGAAGA[A/G]TAATGAAAATGCCCA | 11622 |
rs49089331 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35523922 | AAGGGCAGAGATACC[C/T]CCTGTGTCAGGGAAG | 11622 |
rs49149079 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529609 | GGATTCATGATGACA[A/G]AATACAATACTTTCT | 11622 |
rs49212886 | snp | A/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536759 | TAAGAGTTAAAATTG[A/T]TAGTTTTCTCAACTA | 11622 |
rs49219005 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35531601 | AAAAATAGTACGGTA[G/T]CTGCAAAGTCCTTTC | 11622 |
rs49226762 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Ahr | Mm_Celera | 12:35529281 | TTAAAAAGCCAGGAA[A/G]ATTAAATAGGTCTAG | 11622 |
rs49300653 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35518782 | GTAGGGATATGCTCC[A/C]AGTGTGCAGGGATGT | 11622 |
rs49366745 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35506009 | GATGACATTGTCTTT[C/T]ATCTCCTCAACTGCA | 11622 |
rs49399871 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35520956 | CACACAGGGTGAGTG[C/T]GCAAACAACACACTG | 11622 |
rs49439170 | snp | C/G/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35534446 | CAGTAAAGGTGCAGG[C/G/T]GCCTGAAAGCAGGAT | 11622 |
rs49475383 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35527702 | CGTGCAGCAAGAAGA[A/C]GGAGAGGAAGGAGTG | 11622 |
rs49483486 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35530626 | GTGTCATTAAAGAAG[G/T]TGCAGTGGACAAGTG | 11622 |
rs49499968 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35530161 | TTGGTAATATTTTTA[A/T]GTAAAATACGTGGAT | 11622 |
rs49505343 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35533964 | AGTAGAAATAACTTA[A/G]AAGTCAGTCTAGTTC | 11622 |
rs49511775 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35523722 | TCTAAGCAGCTTCAG[G/T]GCCATCCTCCTGCCT | 11622 |
rs49576196 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35516930 | TTCCCTTGAAGTTTT[A/G]GTATCATAACTATTA | 11622 |
rs49619473 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35521017 | CAACAGCTCTCTTTC[C/T]GGAGAACATCTAGAC | 11622 |
rs49663737 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ahr | Mm_Celera | 12:35521047 | CTTGAGCAATGTGCC[A/G]TTTCTAACAAGAGAA | 11622 |
rs49666202 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35520039 | TTTAACACACTGTAA[A/G]GTTTTCTTCTGCATA | 11622 |
rs49667713 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35530901 | AAAATTCTGTGTTCA[A/G]TGATCCTATCAGTAT | 11622 |
rs49672197 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ahr | Mm_Celera | 12:35508712 | GGATCTACATGCCAT[A/T]GCTCACCGTAGTCTT | 11622 |
rs49684381 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35513768 | CGTCTCCCCAGAGAC[G/T]CAAGGTAATCTCTTT | 11622 |
rs49713914 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35519297 | TAGCATCTGTTAAGC[G/T]GTAATTGACATCCGT | 11622 |
rs49722724 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35506491 | CCGCTGTGGGGCTAA[C/G]GTGAGGCTCACTTGC | 11622 |
rs49740311 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35529193 | GCTGTGATGGACTCT[C/T]TACTGTCCTGTTGGC | 11622 |
rs49875126 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35519560 | ACGTTTTCTAACGTG[C/G]ACTTTCCTCTCTTGT | 11622 |
rs49961601 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35527762 | AGTGCCTTCCCCTCA[C/T]GGCTCAGGGATCTAT | 11622 |
rs49975700 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35506727 | AAAGCCATCTTGACA[C/T]ATTTCCATATGAATT | 11622 |
rs49989263 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35527703 | GTGCAGCAAGAAGAA[A/G]GAGAGGAAGGAGTGT | 11622 |
rs50000478 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35520300 | AAGGGGGGAATTGTG[C/T]TTGTGTTGTGATTAT | 11622 |
rs50026772 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35523583 | ATGTGCCTGGCACTG[C/G]TAATGAGGCTGACTT | 11622 |
rs50032368 | snp | A/C | 0.32 | 0.24 | intron-variant | Ahr | Mm_Celera | 12:35524999 | TGCAGTCCTCTGAGA[A/C]ACATTACAGATATGA | 11622 |
rs50047349 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35520550 | TGTTGTTACCTTGAC[C/T]CAACAAGAGTGAAGT | 11622 |
rs50053407 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35521153 | AAGTGTAGCATCACT[C/T]CCACAGACGAGTTCA | 11622 |
rs50062628 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35523928 | AGAGATACCCCCTGT[A/G]TCAGGGAAGAGTGAA | 11622 |
rs50091062 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ahr | Mm_Celera | 12:35519073 | CTAACCATTCCCTCA[C/T]CTTTAAATGGAGAGC | 11622 |
rs50105852 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525117 | TAGTGACGTATAAGC[A/G]CACAACAGTTTGAGG | 11622 |
rs50106884 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35528227 | TATGGGTCTGAGCTA[A/G]GACCTCTGCATATAC | 11622 |
rs50119593 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35523281 | ACCTTTAAAAATTCG[C/T]TCTGGGCACAATGGA | 11622 |
rs50139653 | snp | A/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536625 | GGATCCTGTGGGAGC[A/G]AGCAGAGCAGCAGGA | 11622 |
rs50151845 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35521265 | AGGACAGATGAGTAA[C/T]TCACATGAGAACAAC | 11622 |
rs50163118 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahr | Mm_Celera | 12:35513321 | AGCACAGAAGGAAAA[A/G]CCCACTTGTTGGACC | 11622 |
rs50188636 | snp | C/G/T | 0.277778 | 0.248452 | intron-variant | Ahr | GRCm38.p3 | 12:35516837 | CCCCTACAAAACATG[C/G/T]CTGTGCTGTCTCGGA | 11622 |
rs50200906 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35527249 | ATTTGGCTTTTGAAA[G/T]TGTAATGCTGAGTGA | 11622 |
rs50202400 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35523771 | ATGTACTTTCTCAAA[C/T]ATCATAAACTTTATT | 11622 |
rs50204226 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35521232 | CGTTCTCTGTTAAAA[C/T]AAATGTCAGTATTCT | 11622 |
rs50261103 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35521634 | GGACTTTTGAAGTTA[C/G]ACTGAATGCACTTTG | 11622 |
rs50310274 | snp | C/G/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518747 | TGTGCTCCCAGTGAG[C/G/T]AGGGATGTGCTCCCA | 11622 |
rs50339248 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35533733 | AACTCCAAGGTAATT[A/C]TGAATGAATGCATCA | 11622 |
rs50362405 | snp | A/G | 0.5 | 0 | intron-variant | Ahr | Mm_Celera | 12:35516720 | GATCCACTGCAAGCA[A/G]ACCAGACACTATTTC | 11622 |
rs50403663 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35530120 | CAAACACAGTCACAA[C/T]ATACCAGCTCAACCA | 11622 |
rs50410268 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35530520 | GAAATGGGGGCTGGA[A/G]GGACTCTAAGAAAAA | 11622 |
rs50458852 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35520493 | TAGTAGAAATGTCTG[C/T]TTGTGTGTGGCCTTT | 11622 |
rs50460940 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ahr | Mm_Celera | 12:35529817 | AAGACATTGACATAG[C/T]CAAAAACAATGAAAG | 11622 |
rs50496741 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ahr | Mm_Celera | 12:35516141 | TAAGGACTCTGCTAC[C/T]TCACCAAGCAGAGAA | 11622 |
rs50508702 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35519406 | GTTAAGGATGCCTTT[C/G]TTCCTCTGAAGGCCA | 11622 |
rs50529974 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529628 | ACAATACTTTCTGCA[A/G]CTACCCCTCCTTCAG | 11622 |
rs50584741 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35516440 | TGTCCTGTTTGCTAC[A/T]GGGCTTGTATTGAGA | 11622 |
rs50587668 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35531616 | GCTGCAAAGTCCTTT[A/C]ATGTCAGGTGCTGTC | 11622 |
rs50616981 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Ahr | Mm_Celera | 12:35519905 | TGGCTTAAGAAACAC[A/G]GTTTTTATTAATTTA | 11622 |
rs50619331 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533367 | CTGCTGAGTCAACGA[C/T]ATTTGCGTCCTTTAA | 11622 |
rs50626055 | snp | A/G | | | utr-variant-5-prime | Ahr | Mm_Celera | 12:35534744 | TGCGGGCGACAGAGG[A/G]GACTCGGGCTGCCCG | 11622 |
rs50651961 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35520501 | ATGTCTGCTTGTGTG[C/T]GGCCTTTGGCGGGGC | 11622 |
rs50655641 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35520476 | ATGCATTAACACAAC[A/C]ATAGTAGAAATGTCT | 11622 |
rs50699435 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35530213 | ACAATGTGAATGTAA[G/T]TCACAAAAAAATTTA | 11622 |
rs50707886 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35519003 | GACGTGATAAACTCT[A/T]CCTTGTCACATGCCC | 11622 |
rs50708439 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35534065 | CCAAAGAGTGGCTAA[A/G]AATGCCACCAAGCTG | 11622 |
rs50730420 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35521879 | CAACCTATAGATCAG[A/C]TGTGGGCTCTCCATT | 11622 |
rs50752544 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35512541 | TTCAAAACCTGACCA[G/T]CCTCAGAGTTTCTCT | 11622 |
rs50752949 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35534495 | TTGGTTGAGACTCAG[C/T]TCCTGGATGGCGGCA | 11622 |
rs50754365 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35512557 | CCTCAGAGTTTCTCT[C/G]CCTGGCCCTGATCTG | 11622 |
rs50791150 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Ahr | Mm_Celera | 12:35521140 | CCCATCTGAGTTAAA[C/G]TGTAGCATCACTTCC | 11622 |
rs50791996 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35530093 | GGCAGCATAAAATCC[G/T]ACTACTGCACACAAA | 11622 |
rs50834897 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35526580 | TTTGCACTCATGGAT[A/G]GTTTTTTTTTTTTTT | 11622 |
rs50849865 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ahr | Mm_Celera | 12:35506753 | GAATTCCATTAACCA[C/T]CAGCTGTGACAATAT | 11622 |
rs50875595 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35509071 | AAAGTGCACTGATTC[C/G]TGAGGCTTAATGTAA | 11622 |
rs50927341 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35532959 | GTAACTTAATCTAAA[A/G]GGAAGTGTTGTCGTG | 11622 |
rs50939052 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35533019 | AAACTAAGAGCACTC[A/G]CCGTTATAATGAATA | 11622 |
rs50980963 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35521907 | ATTACTGCCTTCTTC[A/G]GTCTTCTCCATCATA | 11622 |
rs51023552 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35534451 | AAGGTGCAGGTGCCT[A/G]AAAGCAGGATTTTTT | 11622 |
rs51056798 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Ahr | Mm_Celera | 12:35519016 | CTACCTTGTCACATG[C/T]CCTGGAAGCACTACT | 11622 |
rs51131831 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ahr | Mm_Celera | 12:35529564 | AAGTGTTCCTAGAGA[C/T]GCGGGTGTTAAACAG | 11622 |
rs51182697 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35519004 | ACGTGATAAACTCTA[C/T]CTTGTCACATGCCCT | 11622 |
rs51184424 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35522086 | AAATTTCAATAAGTA[A/G]TAAGAAAACCTCATT | 11622 |
rs51215921 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ahr | Mm_Celera | 12:35515753 | AGCTAGGGGTCACGT[A/G]AGTCATTCTTGTGTT | 11622 |
rs51268378 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ahr | Mm_Celera | 12:35519761 | TTTTATAACATTTAT[C/T]ACTTCCTATCATTAA | 11622 |
rs51297031 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ahr | Mm_Celera | 12:35531108 | AGTGTCTGTCTGTCA[C/G]GCCTGCAACACATAA | 11622 |
rs51312833 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529856 | CATATTTAACCTAAA[A/G]CTCTGAGGCCAGGAA | 11622 |
rs51337690 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35520333 | GAAGGTTATTGTTTT[A/T]AGCAGATCATTTTTA | 11622 |
rs51397133 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35527841 | TTCAGACATAACAGG[A/G]CAGAGGACATATCAA | 11622 |
rs51406056 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ahr | Mm_Celera | 12:35527082 | AAAAATACCAAGAAA[C/T]CCATAGCATTCATGC | 11622 |
rs51446877 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35532915 | CCGAAATTATCAAAT[A/G]CAAATAGTGAGACAA | 11622 |
rs51494124 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35527823 | CCAAAGGCAGTGGAT[A/G]ACTTCAGACATAACA | 11622 |
rs51519389 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529567 | TGTTCCTAGAGACGC[A/G]GGTGTTAAACAGAAG | 11622 |
rs51521500 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ahr | Mm_Celera | 12:35521528 | GTCTCCATGACATGG[A/G]AAGGAGACATTACGA | 11622 |
rs51586415 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35507060 | TCATAATAATCATAT[C/T]GTAACCATTACTGCA | 11622 |
rs51595631 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35531181 | GCCTTCGGGTTTACT[C/T]GACCTTCTGCTTTCC | 11622 |
rs51626876 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35531119 | GTCAGGCCTGCAACA[C/T]ATAACCAGCAGTAGT | 11622 |
rs51697813 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35516279 | AATACGGTGTCAGGA[A/C]AAAAAGACCTCAATT | 11622 |
rs51773056 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531009 | CTGTTAAAGACCTGC[A/G]TAGTGCTCACTCCTA | 11622 |
rs51790402 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533228 | CAAGCACTTGAAAGC[C/T]TCGGAAACTGTAACT | 11622 |
rs51791076 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35529886 | AGAGATGAAGCAAAC[C/T]CGGGAGAGATGGAAA | 11622 |
rs51800460 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Ahr | Mm_Celera | 12:35527360 | GAGTTAGTCTTCTCA[A/C]GCAGACTAAGTAAGA | 11622 |
rs51802882 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ahr | Mm_Celera | 12:35523743 | CCTCCTGCCTCTAAA[C/G]AGGGGACAATGCATG | 11622 |
rs51825976 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ahr | Mm_Celera | 12:35525757 | GGAGGAGAGAAAGGT[A/G]TATATTAATTTGTAT | 11622 |
rs51833221 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35521274 | GAGTAACTCACATGA[C/G]AACAACTGCAATTAT | 11622 |
rs51853104 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ahr | Mm_Celera | 12:35531660 | CATACTGTAGATCTG[C/T]GGAAAATTTAGTATT | 11622 |
rs51870951 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35514081 | GTCAGTCACTAGGGG[A/G]TTATATGGTCACTCT | 11622 |
rs51896298 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ahr | Mm_Celera | 12:35519514 | AGCACCCATGGCTCC[A/G]GTCTGAACTCAACTG | 11622 |
rs51945973 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35521013 | CAAGCAACAGCTCTC[A/T]TTCCGGAGAACATCT | 11622 |
rs51992844 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ahr | Mm_Celera | 12:35520756 | CAACTCTACAAATCA[C/T]ACGCCTCTCTCTGAA | 11622 |
rs52043065 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ahr | Mm_Celera | 12:35520312 | GTGTTTGTGTTGTGA[C/T]TATTGGAAGGTTATT | 11622 |
rs52133085 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35509454 | AGAGAGAGAGAGAGA[C/G]AGACAGACAGACAGA | 11622 |
rs52158667 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Ahr | Mm_Celera | 12:35507689 | CTAATTTTCAATTTT[A/T]GTCTTTTTTCTTAAC | 11622 |
rs52166654 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35528572 | ATTAAAATTGAATAC[A/G]CAAGCATACACATAC | 11622 |
rs52231794 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35507684 | GGCTACTAATTTTCA[A/G]TTTTAGTCTTTTTTC | 11622 |
rs52401370 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ahr | Mm_Celera | 12:35505252 | AAAAGAAATGGACAA[C/T]AGCAAATCAATAAAT | 11622 |
rs52407967 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35528579 | TTGAATACACAAGCA[C/T]ACACATACATACAGA | 11622 |
rs52487347 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35525971 | AAGGAGAGAGAAAAG[C/T]ATATATGTGTGTCAG | 11622 |
rs52497008 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35528607 | AGAGAGGGGGAGGGA[C/T]GAGGGGTGTTGGGAG | 11622 |
rs107610981 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35531232 | CAGTGGAGGAGACTG[C/T]CCTGCTAGTAAAAAC | 11622 |
rs107614312 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35531334 | ATGGTGTGGGGAGAG[A/T]AGAAGGGAGGGCCTA | 11622 |
rs107667213 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531546 | ACATCCACAGCCTCG[A/G]CATAGATGCCCTCTC | 11622 |
rs107704729 | snp | A/G | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35500086 | TGTTGTTGTTTTCTG[A/G]TTTTTTTCTTTTTTT | 11622 |
rs107755584 | snp | A/C/T | | | intron-variant | Ahr | Mm_Celera | 12:35517270 | GAAGGGATGTGCTCC[A/C/T]AGTGTGCAGGGATGT | 11622 |
rs107767222 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35516702 | GGAATGGTCACTGGA[C/T]GGGATCCACTGCAAG | 11622 |
rs107802429 | snp | A/G | | | utr-variant-5-prime | Ahr | GRCm38.p3 | 12:35534889 | ACGGACTCGGGGGTG[A/G]CTGCCAGGCAGGGTT | 11622 |
rs107947667 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531402 | ATATTGTATGAAAAA[A/G]AGAATTTTAATACAG | 11622 |
rs108038831 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35516619 | AGAGCAAGCTCCTCC[G/T]AAGGAATAGCTCAGA | 11622 |
rs108039587 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531090 | GGGAAAATAAGATCC[A/G]GCAGTGTCTGTCTGT | 11622 |
rs108046436 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35516393 | AGATACTTGGTTTAT[G/T]TTTGTACGGCTAATG | 11622 |
rs108074366 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35517211 | ATCAGAGCTGCCAAA[A/G]TTTAAGAGGTAAAGC | 11622 |
rs108082915 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35531253 | TAGTAAAAACAAaaa[A/C]caaaacaaaataaaa | 11622 |
rs108137558 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35516840 | CTACAAAACATGGCT[C/G]TGCTGTCTCGGAAAG | 11622 |
rs108157896 | snp | C/G | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499954 | AACCTTTYTATGACC[C/G]CGCTGTGTGTGCACT | 11622 |
rs108197956 | snp | A/G | | | utr-variant-3-prime | Ahr | GRCm38.p3 | 12:35500508 | TACCAGAACTGTGAG[A/G]GTTGGACATCAGTAC | 11622 |
rs108202404 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35516062 | ATTCTTACCTAGTGT[C/T]GCTGCTTGCTTTGAT | 11622 |
rs108265899 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531109 | GTGTCTGTCTGTCAG[A/G]CCTGCAACACATAAC | 11622 |
rs108298835 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35516965 | CCCTTCGTATAATGC[A/G]AGTCTCTGCACTAAT | 11622 |
rs108323345 | snp | C/T | | | utr-variant-5-prime | Ahr | GRCm38.p3 | 12:35534823 | AGCCCTAGAGCACTG[C/T]GGCCCCTCCTGACCC | 11622 |
rs108417144 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35517206 | ACTCCATCAGAGCTG[C/T]CAAAGTTTAAGAGGT | 11622 |
rs108457319 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35517164 | TTGTTTGATATACTA[C/T]GAAACTAAGACATAG | 11622 |
rs108485770 | snp | A/C | | | synonymous-codon | Ahr | GRCm38.p3 | 12:35511105 | GGCGGAATTCCAGCG[A/C]CAGCTTCACTGGGCT | 11622 |
rs108624454 | snp | A/G | | | synonymous-codon | Ahr | GRCm38.p3 | 12:35511114 | AGAAGACCGGGCGGA[A/G]TTCCAGCGCCAGCTT | 11622 |
rs108675506 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35522297 | AACTAACTAACTAAC[G/T]AAAATCCTGTGGTTG | 11622 |
rs108710489 | snp | A/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535939 | AGAGGGAAGGTCGCT[A/G]TTAACCACCAAAGAA | 11622 |
rs108804732 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35516974 | TAATGCAAGTCTCTG[C/T]ACTAATACTCTCTCT | 11622 |
rs108851513 | snp | A/C | | | upstream-variant-2KB | Ahr | GRCm38.p3 | 12:35535002 | GGAGCGGGCTCGCGG[A/C]GGGCGGCAGCGTGTG | 11622 |
rs108874429 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35510535 | AAACAAAAGAAAACA[A/C]AACAGTACTGCTTTG | 11622 |
rs108911442 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35516601 | GTGGAGATGGTGAAC[A/G]TAAGAGCAAGCTCCT | 11622 |
rs108927609 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35516628 | TCCTCCTAAGGAATA[A/G]CTCAGAGTTTTCGTC | 11622 |
rs211792704 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35519494 | CTGTCAAGTAGCCAT[C/G]CCCCAGCACCCATGG | 11622 |
rs211824428 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35527748 | GGGATGTTTACAACA[C/G]TGCCTTCCCCTCATG | 11622 |
rs211893817 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35528407 | TATTGCAATTTCTTA[C/T]GCCATGCTGGGTTGA | 11622 |
rs212098596 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35532795 | GACCTTTAAGGCATT[G/T]GAAGGCTCAGAGTTG | 11622 |
rs212100190 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35526273 | AAAGTCATGCAAGGC[A/G]ACACATTAAGTGGGT | 11622 |
rs212164941 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35533802 | GAATCTCTTTTCTGA[-/G]GGGGGAAAAAAAATC | 11622 |
rs212175898 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35520799 | AGGATCTAGACTTAG[A/G]AAAATAATTTAGAAA | 11622 |
rs212188256 | in-del | -/TAATGCGTTCTCCCATA | | | intron-variant | Ahr | Mm_Celera | 12:35507838 | GTCTGTCATTTATTC[-/TAATGCGTTCTCCCATA]TAAAAGGTGGGAAAA | 11622 |
rs212258759 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35513964 | GTGCAGATTGCCAGT[G/T]GAGTGTGGTACCTGA | 11622 |
rs212298571 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35526602 | TTTTTTTTTTTTTGT[C/T]TTGTCACCAACATTT | 11622 |
rs212471055 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35530246 | ATCTAATTTGACACT[A/G]TATCTGACTGTAACA | 11622 |
rs212516516 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35520235 | GAAAGCAGTAAGTGC[C/T]CCTAGCCACTGAGCC | 11622 |
rs212675095 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35524274 | GAAACCTGGGCTCAG[A/C]GATAGCTCTCCCAGG | 11622 |
rs212727628 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35514549 | AAAATTTTAAGAACC[C/T]ATCCACCATCAAACC | 11622 |
rs213057022 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35500989 | GAAATTATGTGACAT[-/G]GGGGTGTCAAAGGGT | 11622 |
rs213064071 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35501469 | TCTTGGGGATAAATG[A/C]GAAAGGAAAGGTTCT | 11622 |
rs213197231 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35501985 | TCTACAGAAACTTCA[C/T]ATTGTGGTGTAGTTG | 11622 |
rs213264242 | in-del | -/G | | | utr-variant-5-prime | Ahr | Mm_Celera | 12:35534749 | CGACAGAGGAGACTC[-/G]GGGCTGCCCGAGCTG | 11622 |
rs213467208 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35509116 | CTGCCTGTGGCTGCA[C/G]TATCACAGTCACTCT | 11622 |
rs213596263 | in-del | -/TATATGTG | | | intron-variant | Ahr | GRCm38.p3 | 12:35519866 | ACACATAAACATATA[-/TATATGTG]TGTGTGTATAATAGA | 11622 |
rs213635184 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35520393 | TCCAAATTTCAAGTG[-/A]AAAACTCACTTCCAA | 11622 |
rs213715216 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35526930 | TGTCTAACATTAAAA[C/T]GTCCCCTCAGGGACT | 11622 |
rs213781099 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35532827 | TTAAAGGTGTTCAGT[A/T]CAGATCTGATAAACA | 11622 |
rs213791074 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35527697 | GCAAACGTGCAGCAA[-/G]AAGAAGGAGAGGAAG | 11622 |
rs213809644 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35525093 | ACTTCTGCATCTCAT[C/T]GTGATGCCTAGTGAC | 11622 |
rs213997711 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35520136 | TACCACATGGATGCT[A/C]GTCCTCTCAGAAGAG | 11622 |
rs214001110 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35532163 | TTCTGCCTTTGAAGA[C/T]GAGGATATGGGCTAG | 11622 |
rs214005873 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35525854 | GCATGTGTGACAGAG[A/T]GTGTGTGTGTGTGTG | 11622 |
rs214463572 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35531065 | AAGGAGACTGTACTG[G/T]TCTCTGCTGGGGAAA | 11622 |
rs214555993 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35528531 | TGGAGGTGGAGGAAA[A/C]TGTGGTTGGGATGTA | 11622 |
rs214715217 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35517256 | CTTGCTCCCAGTGTG[A/G]AGGGATGTGCTCCCA | 11622 |
rs214735641 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35509599 | TGTGTGCTTATGTGT[A/G]TGGGTGTGGGTGTGA | 11622 |
rs214744925 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35523467 | AACCAGCAAAGTAGC[C/G]TAAAAGTAAGCATGA | 11622 |
rs214849520 | snp | G/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35529383 | CATGTTCTTTTTTTA[G/T]GATAATCAACTGGTA | 11622 |
rs214975334 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35511943 | GTGGTATGCAGACCC[A/G]GAGCCTTGTGAGTTT | 11622 |
rs214982293 | in-del | -/TCCATCATAATGA | | | intron-variant | Ahr | Mm_Celera | 12:35521913 | CCTTCTTCGGTCTTC[-/TCCATCATAATGA]TCCATCATAGCTCAC | 11622 |
rs215101578 | in-del | -/AA | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35498768 | TTAATTTTCTAAAAG[-/AA]AAAAAAAGAAGAGTC | 11622 |
rs215212436 | snp | C/G | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499953 | GTGCACACACACAGC[C/G]GGGTCATAGAAAGGT | 11622 |
rs215262813 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524957 | TTAAATCATATAAAC[A/G]CACATCTGAAGGGGG | 11622 |
rs215416507 | in-del | -/GGG | | | intron-variant | Ahr | Mm_Celera | 12:35533801 | GAATCTCTTTTCTGA[-/GGG]GGGGGGAAAAAAAAT | 11622 |
rs215747593 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533596 | TGTTGTTTTTGTTTT[C/T]TTTTTTTGGTTCACT | 11622 |
rs215853752 | in-del | -/C | | | utr-variant-5-prime | Ahr | Mm_Celera | 12:35534711 | CCGCCGAGGGCGGGA[-/C]CGACCGCGACGCGCA | 11622 |
rs216149061 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35530765 | AATAACCAAAGTCCA[A/G]TTTTCCACTTATTAC | 11622 |
rs216287382 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35513919 | GCAAGCCTGGAACCC[A/T]ACAGGGCAAACGCCA | 11622 |
rs216502149 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35529673 | ACAACGGCAGAAATC[C/T]TGTCTTTCACACACC | 11622 |
rs216625411 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35521381 | GAAGAGGTAACGGCC[A/G]TGTGACACAGAATGG | 11622 |
rs216626190 | in-del | -/AAAACAAAAC | | | intron-variant | Ahr | GRCm38.p3 | 12:35531265 | AAAACAAAACAAAAT[-/AAAACAAAAC]AAAACAAAAACTTGA | 11622 |
rs216896125 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531749 | TTAATAGAGTGAAGG[A/G]CTTCTATATTACTTC | 11622 |
rs216949545 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35509060 | AATACACTAACAAAG[C/T]GCACTGATTCGTGAG | 11622 |
rs217052763 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35520177 | CCCCAGAGACACTTG[C/T]GAGCCCTCATATGGG | 11622 |
rs217107054 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35528347 | TTTCTTCCTACTGGG[C/T]CGTCTTGTTCAGACT | 11622 |
rs217314686 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35529400 | ATAATCAACTGGTAA[C/T]TTAGTAAACCTCAAA | 11622 |
rs217397826 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35513167 | AAATCTAAAGTCTAA[A/G]CAGGTATATGAATAG | 11622 |
rs217647013 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35531004 | GAATACTGTTAAAGA[C/T]CTGCGTAGTGCTCAC | 11622 |
rs217806036 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35523582 | AATGTGCCTGGCACT[G/T]GTAATGAGGCTGACT | 11622 |
rs217811960 | in-del | -/AAAAA | | | upstream-variant-2KB | Ahr | GRCm38.p3 | 12:35535643 | GATGGGAGGAAAAAG[-/AAAAA]AAAAAAAAAAGATAA | 11622 |
rs217813951 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35525001 | CAGTCCTCTGAGACA[C/T]ATTACAGATATGAGG | 11622 |
rs217980971 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35518886 | AGCTAACCATTCTCA[C/G]CTCTAGTTTTCTTGC | 11622 |
rs218010124 | in-del | -/TGGG | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536654 | AGTGGGGGAAGGAAT[-/TGGG]GGGGGGGGGGCGTCC | 11622 |
rs218041956 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525561 | GGAGAATGAAACCCG[A/G]CACTGTTGATTCCAT | 11622 |
rs218131969 | in-del | -/AA | | | intron-variant | Ahr | Mm_Celera | 12:35527127 | ACCACTGAGCTGTCC[-/AA]AAAAAAAAAAAAAAA | 11622 |
rs218156091 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35522013 | TCACATAGACAATAA[C/G]CCTAACTAGGACAAC | 11622 |
rs218174114 | in-del | -/A | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536943 | TGTTTGCTATTGGAC[-/A]AAAAAAGAGAGTGTG | 11622 |
rs218371136 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35506114 | ACATTTTTCATCTTT[A/G]TCCTGCTCTTTCTAG | 11622 |
rs218493489 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35517295 | GGATGTGCTCCCACT[A/G]TGCAGGGATGTGTTC | 11622 |
rs218688542 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35519547 | AGTCACTCAATTTAC[A/G]TTTTCTAACGTGCAC | 11622 |
rs218821586 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35500756 | GAAGACCTTAAAAAC[A/G]ACTTTTAGTCTGTTA | 11622 |
rs218875123 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35528988 | AAATGCTACTCATCA[G/T]AAACTACGCGCTTGA | 11622 |
rs218883778 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35531991 | AATCACCAGAGTAGA[-/T]TGTTCCATCTTCTGC | 11622 |
rs219289701 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35533806 | TCTTTTCTGAGGGGG[-/A]GAAAAAAAATCTCCC | 11622 |
rs219480483 | in-del | -/AAAA | | | intron-variant | Ahr | GRCm38.p3 | 12:35530217 | GTGAATGTAAGTCAC[-/AAAA]AAAAAAATTTATAAT | 11622 |
rs219570624 | in-del | -/TA | | | intron-variant | Ahr | Mm_Celera | 12:35502137 | GACCACTGAGCTAGC[-/TA]TACTCTTGACCTTTT | 11622 |
rs219594839 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35523923 | AGGGCAGAGATACCC[C/T]CTGTGTCAGGGAAGA | 11622 |
rs219649852 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533021 | ACTAAGAGCACTCGC[C/T]GTTATAATGAATAAC | 11622 |
rs219688613 | in-del | -/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35513617 | TCTATTTTGTTAATG[-/T]TTTTTTTCAAGGTCA | 11622 |
rs219704867 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35519056 | ATAAACTGCACTGGG[G/T]GCTAACCATTCCCTC | 11622 |
rs219755357 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524649 | ACTACTGTAAGAGTC[A/G]CTGTACACTGTAGAT | 11622 |
rs219777901 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35519363 | AATCTAAAAGTCGCC[C/G]AAGATAAGGATAGTA | 11622 |
rs219937734 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35521155 | GTGTAGCATCACTTC[C/T]ACAGACGAGTTCATA | 11622 |
rs220049161 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35515381 | GTACAAATCTTAGTT[C/T]TGCCATTTACTAGAC | 11622 |
rs220056193 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35507653 | TTTAGTTTTTTTTTT[A/T]AATTTTCTTGCTTAT | 11622 |
rs220138903 | in-del | -/C | | | intron-variant | Ahr | Mm_Celera | 12:35516821 | CTCCATTCCCAGGGT[-/C]CCCCTACAAAACATG | 11622 |
rs220184306 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35514112 | GAGATTATAGAGTCT[C/T]ACCCTATTTCCAGTT | 11622 |
rs220194181 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35514037 | CTCAATTTGGTGGAG[C/T]TGTTTGAGGTGCGGC | 11622 |
rs220225945 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35519486 | GTATAGCACTGTCAA[A/G]TAGCCATGCCCCAGC | 11622 |
rs220238838 | in-del | -/AAAAAGAA | | | intron-variant | Ahr | Mm_Celera | 12:35533281 | CAAACATGTTTTAAC[-/AAAAAGAA]AAAAAGAAACCGTCC | 11622 |
rs220448496 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35519815 | TCCTTGACAACACTG[G/T]TGTACACATAAGAAT | 11622 |
rs220635865 | snp | C/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536896 | TAAATGGGGCAACCT[C/G]TGAGGTAGAAACTGG | 11622 |
rs221077211 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35517287 | GTGTGCAGGGATGTG[C/T]TCCCACTATGCAGGG | 11622 |
rs221096723 | in-del | -/TGAAATCTTCAT | | | intron-variant | Ahr | Mm_Celera | 12:35528921 | CAACTCTTAATTCCA[-/TGAAATCTTCAT]TTTGTTCCCCCAGCT | 11622 |
rs221124087 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35516886 | CACTTTTCAAGCCTG[A/C]CCGAATCATTTTAAC | 11622 |
rs221132008 | in-del | -/AAGAA | | | intron-variant | Ahr | Mm_Celera | 12:35534197 | AGAAAGCTAGGCGCT[-/AAGAA]CAGAAAGACATTCCT | 11622 |
rs221258766 | in-del | -/CATCAATTCCTA/CATCTATCCCTA | | | utr-variant-3-prime | Ahr | GRCm38.p3 | 12:35500426 | CCATCGTATAGGGAG[-/CATCAATTCCTA/CATCTATCCCTA]CATCTCAGGTACGGG | 11622 |
rs221402591 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35514050 | AGCTGTTTGAGGTGC[A/G]GCCTTGCTGGAGGAA | 11622 |
rs221440134 | in-del | -/TTT | | | intron-variant | Ahr | Mm_Celera | 12:35526582 | TGCACTCATGGATAG[-/TTT]TTTTTTTTTTTTTTT | 11622 |
rs221499201 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35531089 | GGGGAAAATAAGATC[C/T]GGCAGTGTCTGTCTG | 11622 |
rs221612215 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35532335 | ATAACTGTCATGGTG[A/G]GACCGGCCACTAGAG | 11622 |
rs221862136 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531166 | ACTGGGTCTCCAGCA[A/G]CCTTCGGGTTTACTT | 11622 |
rs221912218 | in-del | -/ACACAC | | | intron-variant | Ahr | Mm_Celera | 12:35502499 | TATGTTTGTATGTAT[-/ACACAC]ACACACACACACACA | 11622 |
rs222140148 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35526290 | CACATTAAGTGGGTA[C/T]TGGAGATTTGAACGC | 11622 |
rs222313982 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35527815 | CCTGAGAGCCAAAGG[C/T]AGTGGATGACTTCAG | 11622 |
rs222315265 | snp | C/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535218 | CCTGTTTTCCAGCCT[C/T]AAAAGGGGTGTGAGG | 11622 |
rs222400175 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35525653 | TTAATTTAAAGCTGT[A/C]GAAGTCTATATAACT | 11622 |
rs222471368 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35531566 | GATGCCCTCTCACTA[A/T]TGCTATCTGAGAGAA | 11622 |
rs222475859 | in-del | -/AGGGCTC | | | intron-variant | Ahr | Mm_Celera | 12:35524348 | AGTGACACAGAGTGA[-/AGGGCTC]AGTGCGATGGAACTG | 11622 |
rs222506328 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35509659 | GTTTATATGGTAAAC[A/G]TCGTGTGTATGTGTG | 11622 |
rs222690728 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35527753 | GTTTACAACAGTGCC[C/T]TCCCCTCATGGCTCA | 11622 |
rs222692185 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35531520 | GACACATCCATGGGT[G/T]AGCATGAGGCACATC | 11622 |
rs222692516 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35525163 | ATTCACTACAATTCG[C/T]GAAAGAATATGATCC | 11622 |
rs222777510 | in-del | -/AAAG | | | intron-variant | Ahr | Mm_Celera | 12:35510511 | TAAAAACAAAGAAAC[-/AAAG]AAAGAAAGAAACAAA | 11622 |
rs222866708 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35533805 | CTCTTTTCTGAGGGG[-/A]GGAAAAAAAATCTCC | 11622 |
rs222991979 | in-del | -/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536653 | GAGTGGGGGAAGGAA[-/T]TGGGGGGGGGGCGTC | 11622 |
rs223274031 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35505825 | AAATTCTGTTGGCTA[A/G]CTTGATAGTCAAAAG | 11622 |
rs223382432 | in-del | -/ACACACACACACACACACAC | | | intron-variant | Ahr | Mm_Celera | 12:35502498 | TATGTTTGTATGTAT[-/ACACACACACACACACACAC]ACACACACACACACA | 11622 |
rs223392222 | in-del | -/AGAGACAGAC | | | intron-variant | Ahr | GRCm38.p3 | 12:35509453 | AAGAGAGAGAGAGAG[-/AGAGACAGAC]AGACAGACAGACAGA | 11622 |
rs223523466 | snp | A/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535881 | AAGACCAATGGCACA[A/G]CCATGGGGATGAGAG | 11622 |
rs223777239 | in-del | -/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35530295 | GTATATAAACCCTTG[-/C]CCCCCCAAATTCCAC | 11622 |
rs223845360 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35533125 | CTTAGACACTCAAGC[A/G]GAGCTCCAAGTTTTA | 11622 |
rs223865413 | in-del | -/TGTGTGTGTGTG | | | intron-variant | Ahr | GRCm38.p3 | 12:35519867 | ACATAAACATATATA[-/TGTGTGTGTGTG]TATGTGTGTGTGTAT | 11622 |
rs223920548 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35502562 | ATGTGCAACACAAGT[A/G]TGCAGTGCTCAAGGG | 11622 |
rs223934760 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525805 | AAATGGGGAGAGGGA[A/G]AGAATGTCAAAGAAA | 11622 |
rs223937304 | in-del | -/CATAT | | | intron-variant | Ahr | Mm_Celera | 12:35521204 | CTAAGGGTCCCTAGG[-/CATAT]CCAGTCACAAGGCGT | 11622 |
rs224045256 | in-del | -/T/TT/TTT | | | intron-variant | Ahr | Mm_Celera | 12:35513616 | TCTATTTTGTTAATG[-/T/TT/TTT]TTTTTTTTCAAGGTC | 11622 |
rs224205377 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35530565 | AAGCAGGAGATGGGC[A/T]GGCACAGACTGAGTC | 11622 |
rs224262683 | in-del | -/TGGT | | | intron-variant | Ahr | Mm_Celera | 12:35505323 | TGTCAGCTGTAACAA[-/TGGT]TCAATGGTTTTATGA | 11622 |
rs224423572 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35529880 | CCAGGAAGAGATGAA[C/G]CAAACCCGGGAGAGA | 11622 |
rs224487494 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35523265 | AAGAGCATAGAAAAC[A/C]ACCTTTAAAAATTCG | 11622 |
rs224602864 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525425 | AGTGCTGGATGACTG[A/G]CATGTAACAGACAAC | 11622 |
rs224622169 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35527441 | TGATAATCTCTTCTG[G/T]ATTGGATTTCAGACC | 11622 |
rs224661200 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35521827 | CCTGGGGGTTTCAAA[A/C]GCCCAACCAGGCCCA | 11622 |
rs224771012 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35501060 | TGAACTGATTCTATC[C/T]GAACTTCTACACAGC | 11622 |
rs224870503 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35526318 | CGCAGATCTGCATTG[C/T]TTACACACCAAATCC | 11622 |
rs224935538 | snp | A/C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35529110 | AAAGCATCACAGAAC[A/C/T]GTCTGAGACGTCTAC | 11622 |
rs225074694 | in-del | -/AG | | | intron-variant | Ahr | Mm_Celera | 12:35533945 | AAATGAACTACAGGT[-/AG]AGAGTAGAAATAACT | 11622 |
rs225080709 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35524823 | GGGCTCAGTGTACAA[C/T]CACATGAAATCGCTG | 11622 |
rs225105421 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35519509 | GCCCCAGCACCCATG[A/G]CTCCAGTCTGAACTC | 11622 |
rs225171349 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35519231 | GGACCATGTGACAGT[C/T]CGTAGAAATGAAATG | 11622 |
rs225171493 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35525190 | ATCCCTTAAATAGCA[C/T]ATGCCTTAATAACTC | 11622 |
rs225328412 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524682 | CATGGAATCACTACC[A/G]TATGAGTAGGTGTTC | 11622 |
rs225391044 | in-del | -/TAGG | | | intron-variant | Ahr | Mm_Celera | 12:35513005 | AGAAATCCTGACAGT[-/TAGG]TAGGTAACAGGCTGT | 11622 |
rs225404204 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35519763 | TTATAACATTTATCA[C/T]TTCCTATCATTAATT | 11622 |
rs225451260 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35521772 | TTGAGAAACATTAGG[A/G]GGTGGGCCTTATTGA | 11622 |
rs225538198 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35528284 | AGGGGACTCCTAACA[-/G]AGGGAGTAAGGGGTG | 11622 |
rs225668313 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525949 | AAAGAGACAAAGAGA[A/G]GCAAAGAAGGAGAGA | 11622 |
rs225804793 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35517026 | TGTTAAGAAATCTAC[G/T]GAATAATTCCACTGC | 11622 |
rs225865315 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35523442 | AGGTCTTATGTACAC[G/T]GAAGTGTAAAACCAG | 11622 |
rs225996023 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518775 | CCAGTGAGTAGGGAT[A/G]TGCTCCCAGTGTGCA | 11622 |
rs226101589 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35525754 | GGGGAGGAGAGAAAG[-/T]GTGTATATTAATTTG | 11622 |
rs226207641 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35513785 | AAGGTAATCTCTTTA[C/T]TATAACCCCCTATAA | 11622 |
rs226277118 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35520673 | TATCTCACAGATTGG[G/T]CCCTGTCAACTGCTG | 11622 |
rs226393958 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35514295 | TCTAACCCCCCAGTA[C/T]TGTAAGCCCAAGTAC | 11622 |
rs226589695 | in-del | -/AA | | | intron-variant | Ahr | Mm_Celera | 12:35527176 | AAGAGCCTTTAAGTT[-/AA]AAAAAAAAAAACGAT | 11622 |
rs226597779 | snp | C/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535995 | AGTCAGGTAGGTGAT[C/G]CTGGACATGAAGAGA | 11622 |
rs226974964 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35520163 | AGAGGGCATTGGATC[A/C]CCAGAGACACTTGTG | 11622 |
rs226979116 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524600 | TGGAATCACTACTGT[A/G]GGAGTCACTGTATAC | 11622 |
rs227019975 | in-del | -/AA | | | intron-variant | Ahr | Mm_Celera | 12:35527065 | ATACCAAACACTGCC[-/AA]AAAAAATACCAAGAA | 11622 |
rs227100105 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35515946 | GCCAAAAAATAGTGT[G/T]GGGGTAAACTGGTCT | 11622 |
rs227217763 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35509014 | AGATTACAACTCTAA[A/G]TCCATATCAGCAAAA | 11622 |
rs227225284 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35520077 | TATTCTTTTTAAAAT[G/T]TATTATTGTGTGTAA | 11622 |
rs227291856 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35525036 | GCTGCCTGGTGACCT[-/G]GATGGCCATTTTTAG | 11622 |
rs227296360 | in-del | -/CCACA | | | intron-variant | Ahr | GRCm38.p3 | 12:35523105 | CTGGCTTTTACCCCC[-/CCACA]CACACTTTCCATTAA | 11622 |
rs227429555 | in-del | -/ACAG | | | intron-variant | Ahr | Mm_Celera | 12:35507336 | CCCACATGCACACAC[-/ACAG]AGGAATCAAAGGATT | 11622 |
rs227498729 | in-del | -/TTGA | | | intron-variant | Ahr | Mm_Celera | 12:35525210 | TTAATAACTCAATTT[-/TTGA]TTTATGAACATAAAA | 11622 |
rs227513501 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35523812 | ACAAACAAATCAACA[C/T]TCATCGTAAAGGCAC | 11622 |
rs227773759 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35517266 | GTGTGAAGGGATGTG[C/T]TCCCAGTGTGCAGGG | 11622 |
rs227826842 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35531185 | TCGGGTTTACTTGAC[A/C]TTCTGCTTTCCTAGT | 11622 |
rs227835866 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35513753 | ACTCAAATTGTCCAA[A/C]GTCTCCCCAGAGACG | 11622 |
rs228097355 | in-del | -/AAGT | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35498718 | ACTGAAAATGCATAG[-/AAGT]AAGAGATCTTTTTCC | 11622 |
rs228110041 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35519093 | AAATGGAGAGCACTG[A/G]TGCGCATCCAATAGA | 11622 |
rs228127587 | in-del | -/C | | | intron-variant | Ahr | Mm_Celera | 12:35530482 | CAGTTGTTCAAAGTG[-/C]TTCACAGGGAGATGT | 11622 |
rs228224299 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35531899 | CATCTGCTGTTTGCT[-/A]GCAATCCTAAACTAC | 11622 |
rs228261661 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35508879 | CAGCTGATCTACAAG[G/T]CTAAGAGACTATGTG | 11622 |
rs228265457 | in-del | -/CA | | | intron-variant | Ahr | Mm_Celera | 12:35521415 | ACATCCTCTCAAAGT[-/CA]CAGATTGGCATACCG | 11622 |
rs228290545 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35530854 | ATTATTTCCATAGTA[C/T]TATTACAGAAAGGAG | 11622 |
rs228375935 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35514388 | ATACAGCTCCCCTCA[C/T]TTCACCGGCCAGAGC | 11622 |
rs228436067 | in-del | -/GAAAGTAA | | | intron-variant | Ahr | Mm_Celera | 12:35521934 | CATAGCTCACCCTCT[-/GAAAGTAA]GAAATCTCCCAGTTA | 11622 |
rs228551424 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35528360 | GGCCGTCTTGTTCAG[A/G]CTTGATATGAATGAG | 11622 |
rs228737934 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35527314 | GCACAGATTCTCAAA[C/T]TTCCACTTCCTTAAT | 11622 |
rs228757695 | in-del | -/TGT | | | intron-variant | Ahr | Mm_Celera | 12:35502702 | TCTCCAGGCTAGAAA[-/TGT]TGTTATTTTTTTCAC | 11622 |
rs228925040 | in-del | -/TAAC | | | intron-variant | Ahr | Mm_Celera | 12:35534360 | ATTTCCAGGCAAGCT[-/TAAC]TAACTAAGCTAGAGC | 11622 |
rs229064188 | snp | G/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35530226 | AAGTCACAAAAAAAT[G/T]TATAATCTAATTTGA | 11622 |
rs229084707 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35524751 | ACGCTACAAACCACA[C/G]GGAATCACTACTGTA | 11622 |
rs229111311 | in-del | -/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35503467 | ATGATATCCTCCTGA[-/G]GGGGGTAACAAAGAA | 11622 |
rs229142542 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35524102 | CTGAAGCTGCTTGTC[C/T]GGAGACTATGGGCGG | 11622 |
rs229144086 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35530615 | TTTCAGCCTCAGTGT[C/T]ATTAAAGAAGGTGCA | 11622 |
rs229453471 | snp | G/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536938 | AGAAGCTGTTTGCTA[G/T]TGGACAAAAAAGAGA | 11622 |
rs229545225 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35502667 | AAGAAGGGTAAGCAA[A/G]TGTTAATTGCCAAGC | 11622 |
rs229660093 | in-del | -/ACACAC | | | intron-variant | Ahr | Mm_Celera | 12:35528823 | TCCATGTGCACACTT[-/ACACAC]ACACACACACACACA | 11622 |
rs229814115 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35530265 | CTGACTGTAACATTC[A/G]GCTCATCCTTAGAAG | 11622 |
rs229835513 | in-del | -/AGAGAGAGAGAGACAGAC | | | intron-variant | Ahr | GRCm38.p3 | 12:35509454 | GAGAGAGAGAGAGAG[-/AGAGAGAGAGAGACAGAC]AGACAGACAGACAGA | 11622 |
rs230134523 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524601 | GGAATCACTACTGTG[A/G]GAGTCACTGTATACT | 11622 |
rs230365866 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35527749 | GGATGTTTACAACAG[C/T]GCCTTCCCCTCATGG | 11622 |
rs230491135 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35528454 | GATTTTTCTTTTTTT[C/T]TTGGAAGGGAAATGG | 11622 |
rs230622323 | snp | A/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536597 | AATACACATGACACA[A/G]AAGGAGAAGAGGGGA | 11622 |
rs230709570 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35524562 | GAATCATTACTATAG[-/A]ACTACGTAAATTACT | 11622 |
rs230795944 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35526284 | AGGCAACACATTAAG[G/T]GGGTATTGGAGATTT | 11622 |
rs230843277 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533355 | CGGGGTAGAAAACTG[C/T]TGAGTCAACGACATT | 11622 |
rs230904583 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35520955 | ACACACAGGGTGAGT[A/G]CGCAAACAACACACT | 11622 |
rs231023441 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35528527 | GGAGTGGAGGTGGAG[A/G]AAAATGTGGTTGGGA | 11622 |
rs231127842 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524360 | TGAAGGGCTCAGTGC[A/G]ATGGAACTGAAAGGG | 11622 |
rs231160589 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35525882 | GTGTGTCACAGAAAG[A/T]GTGTGTGTGCATCAG | 11622 |
rs231172947 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531830 | CAGCAGATCATGAGA[A/G]CCTTGCTACGGCTGG | 11622 |
rs231249279 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35518940 | ACTTGAGATGAATTA[C/T]GGTGAGTATAAAATA | 11622 |
rs231428992 | in-del | -/A | | | intron-variant | Ahr | GRCm38.p3 | 12:35520800 | GGATCTAGACTTAGG[-/A]AAATAATTTAGAAAT | 11622 |
rs231479672 | in-del | -/C | | | intron-variant | Ahr | Mm_Celera | 12:35530124 | CACAGTCACAATATA[-/C]CAGCTCAACCATTCC | 11622 |
rs231490491 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35532651 | AAAGCTTGGTGACCT[A/G]GTTGTTAAGGGTGAA | 11622 |
rs231724846 | in-del | -/ATTTTGAGAAGAAATT | | | intron-variant | Ahr | Mm_Celera | 12:35519696 | AATGTGGCATGATAC[-/ATTTTGAGAAGAAATT]ATTTATTCTTAACCA | 11622 |
rs231727298 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35527688 | CCACAAGTGGCAAAC[A/G]TGCAGCAAGAAGAAG | 11622 |
rs231920368 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35522366 | TCATTGTTCAACAGA[C/T]ATGATACAGGAGAAA | 11622 |
rs231981850 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35519310 | GCGGTAATTGACATC[C/T]GTGCAGTAGGCTACA | 11622 |
rs231985437 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35529662 | TAAAGGGAAACACAA[C/G]GGCAGAAATCCTGTC | 11622 |
rs232076569 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525340 | AATTAAGGAATTACT[A/G]TGCAAGATAAATTAT | 11622 |
rs232195077 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35519537 | CTCAACTGACAGTCA[C/G]TCAATTTACGTTTTC | 11622 |
rs232213759 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35528132 | CAGAGGGGTCAAAGA[C/T]ACCATGAGAACACTG | 11622 |
rs232333733 | in-del | -/GC | | | intron-variant | Ahr | Mm_Celera | 12:35509522 | TATGTGGTATATGTA[-/GC]GTGTGTGTGTGAGTT | 11622 |
rs232765375 | in-del | -/CA | | | utr-variant-3-prime | Ahr | GRCm38.p3 | 12:35499941 | AAAGGATGAGTAGTG[-/CA]CACACACAGCGGGGT | 11622 |
rs232850685 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525743 | GTGTGTGTATGTGGG[A/G]AGGAGAGAAAGGTGT | 11622 |
rs232865165 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35502854 | GAACCTTTGATTTCC[-/T]TTTTTTCTAGTGATT | 11622 |
rs232910176 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35514044 | TGGTGGAGCTGTTTG[A/G]GGTGCGGCCTTGCTG | 11622 |
rs232930130 | in-del | -/GCATGCAC | | | intron-variant | Ahr | Mm_Celera | 12:35526126 | CATGCACACATGCCT[-/GCATGCAC]ACATGCAGAGGCCAC | 11622 |
rs232956364 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35519930 | AATTTAACAAAAATA[A/C]CTCCAAATCAGTTTA | 11622 |
rs233078717 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35512978 | TGGCGTTAGAGGTGG[-/A]AAACTGTCACTCAGA | 11622 |
rs233188990 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35519724 | ATTATTTATTCTTAA[A/C]CACTGCTATTAATTT | 11622 |
rs233207294 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35519370 | AAGTCGCCCAAGATA[A/G]GGATAGTACAATGCC | 11622 |
rs233237259 | in-del | -/TACT | | | intron-variant | Ahr | Mm_Celera | 12:35519709 | CATTTTGAGAAGAAA[-/TACT]TTATTTATTCTTAAC | 11622 |
rs233425575 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35505056 | ATTTCTAAAAGGAAG[A/T]AAAGGTAAAACGCAC | 11622 |
rs233558142 | snp | G/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536440 | GCCGTGTTAAGCATG[G/T]CAGACACAGAAGGCA | 11622 |
rs233768077 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35516146 | ACTCTGCTACTTCAC[C/G]AAGCAGAGAAGATTT | 11622 |
rs233927579 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35509604 | GCTTATGTGTGTGGG[C/T]GTGGGTGTGATTCAA | 11622 |
rs233992964 | in-del | -/AAG | | | intron-variant | Ahr | Mm_Celera | 12:35522682 | GGACAGTTCAACTGT[-/AAG]AAGATCGATTCATGC | 11622 |
rs234062285 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35523348 | ATTTGCTCAAATACC[A/G]ATTCCTTGGTTTTCT | 11622 |
rs234073425 | in-del | -/A | | | intron-variant | Ahr | GRCm38.p3 | 12:35517111 | TACAATCTAAGTCCC[-/A]TTTAATTTCCAAAAC | 11622 |
rs234128127 | in-del | -/TG | | | intron-variant | Ahr | GRCm38.p3 | 12:35514149 | CTCCCCACCCCCTTC[-/TG]TGTGTGTGTGTGTGT | 11622 |
rs234437860 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35531476 | ATCTGTTGCTTCTTT[C/T]GTTCAGTTTGATGTG | 11622 |
rs234632845 | in-del | -/CTACAGACTGAATGATATCACTGCTGTGAGATCTGATGTGCACTTCAG | | | intron-variant | Ahr | GRCm38.p3 | 12:35524821 | AGGGCTCAGTGTACA[lengthTooLong]ACCACATGAAATCGC | 11622 |
rs234734241 | snp | C/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536714 | TTTCATTAAGCCCAT[C/T]GCTTTGTGTGCTAAT | 11622 |
rs234862623 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35529495 | AGGACCAAACCTATT[C/T]TATAGGGAGGCAAGC | 11622 |
rs234905005 | snp | A/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536222 | CAAATTAAAAACAGA[A/T]CCACAAGATGACCTG | 11622 |
rs234958496 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35531207 | TTCCTAGTTTAGTTG[-/T]TAAGAACAGCAGTGG | 11622 |
rs235045741 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35530319 | ATTCCACCTAAAGAG[C/G]TCTGTCCTATGGAAA | 11622 |
rs235047326 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35522447 | AAATCCATGTATTCA[C/T]AAATAAAGTTCTACT | 11622 |
rs235189700 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35516571 | AGGGCAGGTTTAAAA[A/G]GCATTTCGGAAAGTG | 11622 |
rs235232323 | snp | C/G | | | utr-variant-5-prime | Ahr | Mm_Celera | 12:35534926 | GTTCGTCCTCCGGGT[C/G]GCTCCGGGCTGAGCC | 11622 |
rs235398035 | in-del | -/G | | | utr-variant-5-prime | Ahr | Mm_Celera | 12:35534750 | GACAGAGGAGACTCG[-/G]GGCTGCCCGAGCTGG | 11622 |
rs235427818 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35527712 | GAAGAAGGAGAGGAA[A/G]GAGTGTGCTCGACCC | 11622 |
rs235586339 | in-del | -/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35525208 | GCCTTAATAACTCAA[-/T]TTTTTATGAACATAA | 11622 |
rs235709902 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35517835 | GTGCAGGGATGTGCT[C/T]CCAGTGTGCAGGGAT | 11622 |
rs235749946 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525164 | TTCACTACAATTCGT[A/G]AAAGAATATGATCCC | 11622 |
rs235787065 | in-del | -/AAAAA | | | intron-variant | Ahr | Mm_Celera | 12:35533808 | CTTTTCTGAGGGGGG[-/AAAAA]AAATCTCCCATCTCA | 11622 |
rs235803714 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525637 | TTGACGCTAACATAC[A/G]TTAATTTAAAGCTGT | 11622 |
rs235901018 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35519557 | TTTACGTTTTCTAAC[A/G]TGCACTTTCCTCTCT | 11622 |
rs235903353 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35523830 | TCGTAAAGGCACAAG[-/A]CACTGAAATGTACGA | 11622 |
rs236036809 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35503512 | TCTAAACATCAACTT[A/G]CTTTTAAGAAAATTA | 11622 |
rs236249121 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35509557 | GGGGTTTGTGTGTGT[A/G]AATATGAGTTTATGT | 11622 |
rs236291317 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35502719 | TTGTTATTTTTTTCA[C/T]TGCCGCACAATTACT | 11622 |
rs236342490 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35503259 | AGTCCCATACAATCA[A/G]ACACAGCAGATTCAC | 11622 |
rs236579640 | in-del | -/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35505786 | GCAGTGCTCAGACTC[-/T]TGTCAAGGGTTTGTC | 11622 |
rs236777992 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35519838 | ATAAGAATGACTTAG[A/C]TAATTTGACAAAACA | 11622 |
rs236846771 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35526303 | TATTGGAGATTTGAA[C/T]GCAGATCTGCATTGT | 11622 |
rs236890577 | in-del | -/ACCACA | | | intron-variant | Ahr | Mm_Celera | 12:35523104 | CTGGCTTTTACCCCC[-/ACCACA]CCACACACACTTTCC | 11622 |
rs237000979 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35526599 | TTTTTTTTTTTTTTT[G/T]GTCTTGTCACCAACA | 11622 |
rs237088198 | in-del | -/A/AA/AAA | | | intron-variant | Ahr | GRCm38.p3 | 12:35524875 | ACAGAACGCTTTTGT[-/A/AA/AAA]AAAAAAAATTACACT | 11622 |
rs237122328 | in-del | -/TAAA | | | intron-variant | Ahr | Mm_Celera | 12:35527176 | AAAGAGCCTTTAAGT[-/TAAA]AAAAAAAACGATTTT | 11622 |
rs237142333 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525094 | CTTCTGCATCTCATT[A/G]TGATGCCTAGTGACG | 11622 |
rs237182919 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35516871 | CTTACATTATGCTCG[C/T]ACTTTTCAAGCCTGA | 11622 |
rs237197484 | in-del | -/AAAT | | | intron-variant | Ahr | Mm_Celera | 12:35530224 | TAAGTCACAAAAAAA[-/AAAT]TTTATAATCTAATTT | 11622 |
rs237249088 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35523381 | AGAAGTGACTGAATC[A/G]GCATAGACGAGGCCT | 11622 |
rs237294682 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35516100 | CTTGCTGTAAGGCAC[A/T]GGCTGCTTATAATGC | 11622 |
rs237313848 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35529601 | GACATTCTGGATTCA[C/T]GATGACAAAATACAA | 11622 |
rs237489286 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35513975 | CAGTTGAGTGTGGTA[A/C]CTGAATGGGAACTGC | 11622 |
rs237717371 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35527126 | AACCACTGAGCTGTC[A/C]AAAAAAAAAAAAAAA | 11622 |
rs237750086 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35520477 | TGCATTAACACAACC[A/C]TAGTAGAAATGTCTG | 11622 |
rs237804849 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35521147 | GAGTTAAAGTGTAGC[A/G]TCACTTCCACAGACG | 11622 |
rs237923880 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35523205 | ACACACACACACACA[A/C]ACAAAACCTTCCTTA | 11622 |
rs238150405 | in-del | -/AT | | | intron-variant | Ahr | GRCm38.p3 | 12:35517081 | TCACTCGGTAATGAC[-/AT]ATTGTCTTGGGACTA | 11622 |
rs238157735 | in-del | -/CT | | | intron-variant | Ahr | Mm_Celera | 12:35529147 | TCCCACCGAGTCAGA[-/CT]CTCTTGCCAGTGTCT | 11622 |
rs238170903 | in-del | -/GTGCACTGTGAG | | | cds-indel | Ahr | Mm_Celera | 12:35511081 | CCTTGTGCAGAGTCT[-/GTGCACTGTGAG]GGGTTTAGAGCCCAG | 11622 |
rs238191984 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35508115 | GAAGAATTATGAGTG[A/G]AAAAGTTCCCTTACT | 11622 |
rs238196507 | in-del | -/TTTATTTGGCA | | | intron-variant | Ahr | Mm_Celera | 12:35509218 | CATAAATATAAGCAT[-/TTTATTTGGCA]TTTATTCCAGGCATG | 11622 |
rs238237038 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35519893 | TGTATAATAGAATGG[C/T]TTAAGAAACACGGTT | 11622 |
rs238406395 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529522 | AAGCAAGTATAATAC[A/G]CTGCTCAGTGATGTA | 11622 |
rs238637094 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35505851 | AAAAGGAAGGAGAAA[A/C]CCAGTCAGGATGCTT | 11622 |
rs239008370 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35533282 | CAAACATGTTTTAAC[-/A]AAAAGAAACCGTCCT | 11622 |
rs239096491 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35530530 | TGGAAGGACTCTAAG[-/A]AAAAAAGACATGAAT | 11622 |
rs239149727 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531354 | GGGAGGGCCTAGGAG[A/G]AGTTGAAGGAGGAGA | 11622 |
rs239243335 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35517306 | CACTATGCAGGGATG[C/T]GTTCCAAGTGTGCAG | 11622 |
rs239307373 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35513379 | TAGAACTGTTTCCAC[C/T]CCACAATACCTCCAG | 11622 |
rs239312168 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35525458 | TGAACCATGCAGGCC[C/G]CACTGCCACCCTCAC | 11622 |
rs239441223 | in-del | -/AA | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35500078 | TAGATAGAAAAAAAG[-/AA]AAAAAAATCAGAAAA | 11622 |
rs239563946 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35525526 | ACAGTTAAAGTCAAG[G/T]AGCTGGCCAGTGGCA | 11622 |
rs239704949 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35510550 | CAACAGTACTGCTTT[A/G]GGCTTGGGTCATAGC | 11622 |
rs239769821 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35524664 | GCTGTACACTGTAGA[C/T]CACATGGAATCACTA | 11622 |
rs239770183 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518776 | CAGTGAGTAGGGATA[C/T]GCTCCCAGTGTGCAG | 11622 |
rs239884661 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35530578 | GCTGGCACAGACTGA[A/G]TCCTGAAATGGCAGT | 11622 |
rs239920071 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35516686 | GATAAATGGGTTCCT[-/G]GGAATGGTCACTGGA | 11622 |
rs239948279 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35530171 | TTTTATGTAAAATAC[A/G]TGGATACAGACATGT | 11622 |
rs240123268 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35510494 | TGGTACCAGTGTTGG[-/T]TTTAAAAACAAAGAA | 11622 |
rs240176779 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35514304 | CCAGTACTGTAAGCC[C/T]AAGTACAAGCTCCCT | 11622 |
rs240230704 | in-del | -/TCG | | | intron-variant | Ahr | Mm_Celera | 12:35516638 | AATAGCTCAGAGTTT[-/TCG]TCGTCGTCGGAAGCC | 11622 |
rs240265760 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35515422 | CTTGAGCCTGTTTAC[G/T]GATAATGCGAAAGGG | 11622 |
rs240286673 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35516888 | CTTTTCAAGCCTGAC[C/T]GAATCATTTTAACCT | 11622 |
rs240376285 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35517291 | GCAGGGATGTGCTCC[A/C]ACTATGCAGGGATGT | 11622 |
rs240415316 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35522022 | CAATAAGCCTAACTA[A/G]GACAACATCCAAATG | 11622 |
rs240580100 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524978 | CTGAAGGGGGATGAC[A/G]GTCTTTGCAGTCCTC | 11622 |
rs240708937 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35513588 | CCTTCTTTTACTTCA[C/T]GAGTTCTTCTTTTTC | 11622 |
rs240842920 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35506501 | GCTAAGGTGAGGCTC[A/G]CTTGCTGGCTACAGG | 11622 |
rs240880429 | in-del | -/TTTGA | | | intron-variant | Ahr | Mm_Celera | 12:35506088 | TTATCACTTTTGTCT[-/TTTGA]TTTTTTTTCAACATT | 11622 |
rs240924826 | in-del | -/TTGAG | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499896 | AATAAATAGTGGACT[-/TTGAG]TTATCAATTACTCTT | 11622 |
rs240926667 | snp | A/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536916 | GTAGAAACTGGAACT[A/G]TGATCGAGAAGCTGT | 11622 |
rs241381828 | in-del | -/A | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35498379 | GATTTTATTATTCTT[-/A]AGATGTTTTAGCTAT | 11622 |
rs241568891 | in-del | -/CCCCGG | | | intron-variant | Ahr | Mm_Celera | 12:35523886 | AGTTGAGCCTGAAGC[-/CCCCGG]CCCTGTGCATGAAAT | 11622 |
rs241621620 | in-del | -/TACAGTACAA | | | intron-variant | Ahr | GRCm38.p3 | 12:35506431 | CAAACCCTCCATCAG[-/TACAGTACAA]TACAGTACAGTACAG | 11622 |
rs241631057 | in-del | -/CC | | | intron-variant | Ahr | Mm_Celera | 12:35528770 | CAAGTGAAGAAGACT[-/CC]TGACTCTGGCCTCCG | 11622 |
rs241751499 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35531654 | GGGCCCCATACTGTA[G/T]ATCTGCGGAAAATTT | 11622 |
rs241857436 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35534432 | GGAAGGTCGCTGAGC[A/C]GTAAAGGTGCAGGTG | 11622 |
rs241859700 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35533026 | GAGCACTCGCCGTTA[A/T]AATGAATAACATTTA | 11622 |
rs241884509 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35528785 | TTGACTCTGGCCTCC[G/T]AGTGCATTTGCATAC | 11622 |
rs241997762 | in-del | -/AAG | | | intron-variant | Ahr | GRCm38.p3 | 12:35507932 | CTGAAGCTAAAAATT[-/AAG]AAATATTTTTACAAA | 11622 |
rs242013535 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35526393 | TTAAAGTACTTTATT[-/A]TTTCTTTGTAAAAAT | 11622 |
rs242060931 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524103 | TGAAGCTGCTTGTCC[A/G]GAGACTATGGGCGGT | 11622 |
rs242122938 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35530238 | AATTTATAATCTAAT[C/T]TGACACTATATCTGA | 11622 |
rs242199986 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35507675 | CTTGCTTATGGCTAC[G/T]AATTTTCAATTTTAG | 11622 |
rs242235375 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524821 | TAGGGCTCAGTGTAC[A/G]ACCACATGAAATCGC | 11622 |
rs242262594 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35526265 | CTAAGGTTAAAGTCA[C/T]GCAAGGCAACACATT | 11622 |
rs242334967 | in-del | -/GG | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536655 | AGTGGGGGAAGGAAT[-/GG]GGGGGGGGCGTCCAG | 11622 |
rs242417240 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35520194 | AGCCCTCATATGGGT[A/T]CTGGGAATCAAACCT | 11622 |
rs242450226 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35515946 | GCCAAAAAATAGTGT[-/G]GGGGTAAACTGGTCT | 11622 |
rs242453810 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35509100 | AAGACCTAACTCCTC[G/T]CTGCCTGTGGCTGCA | 11622 |
rs242583129 | in-del | -/ACACACACACACACACAA | | | intron-variant | Ahr | Mm_Celera | 12:35523205 | CACACACACACACAC[-/ACACACACACACACACAA]ACAAAACCTTCCTTA | 11622 |
rs242588895 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35501338 | ACAAAACCAATTTTT[A/T]AAAGAGAATGGTTAT | 11622 |
rs242660751 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35509684 | TGTGTGTGTATGTGA[C/G]TATGTGCACACGCAC | 11622 |
rs242738177 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35509776 | CTCATTCCGCCCTCA[A/C]TGTACCATAGGTGCA | 11622 |
rs243472725 | in-del | -/TTAC | | | intron-variant | Ahr | Mm_Celera | 12:35503352 | ACAGCTCATGAATAG[-/TTAC]TTAATAAACTTCATG | 11622 |
rs243536146 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35528996 | CTCATCATAAACTAC[A/G]CGCTTGATTTGAAAT | 11622 |
rs243575066 | in-del | -/TTTT | | | intron-variant | Ahr | Mm_Celera | 12:35526581 | TGCACTCATGGATAG[-/TTTT]TTTTTTTTTTTTTTT | 11622 |
rs243638187 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35522449 | ATCCATGTATTCATA[A/G]ATAAAGTTCTACTGA | 11622 |
rs243698145 | in-del | -/CTA | | | intron-variant | Ahr | Mm_Celera | 12:35527269 | TGCTGAGTGACTTAC[-/CTA]CTAGTTAATCATTTA | 11622 |
rs243873951 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35531171 | GTCTCCAGCAGCCTT[A/C]GGGTTTACTTGACCT | 11622 |
rs244011509 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35527612 | ACCCACTGATAAGTG[C/T]GTTGCTCAACTCTCG | 11622 |
rs244062207 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35515680 | TGACTCTACAGTCCT[C/T]GAGAATTATTTTATT | 11622 |
rs244322159 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35519232 | GACCATGTGACAGTT[C/T]GTAGAAATGAAATGT | 11622 |
rs244350615 | snp | A/G | | | missense | Ahr | Mm_Celera | 12:35504813 | TTGGGGTTGACTGGG[A/G]AGCCCAGTCTTTCCT | 11622 |
rs244529892 | in-del | -/GAC | | | intron-variant | Ahr | GRCm38.p3 | 12:35509170 | GGTTACTTCTTACAG[-/GAC]GACGCCTCCTATCAG | 11622 |
rs244581510 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35525839 | GGTGTTTGTGTGTGT[G/T]CATGTGTGACAGAGA | 11622 |
rs244635813 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35525455 | CACTGAACCATGCAG[G/T]CCGCACTGCCACCCT | 11622 |
rs244889034 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35514127 | CACCCTATTTCCAGT[A/T]CATTCTCTCCCCACC | 11622 |
rs244933974 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35523466 | AAACCAGCAAAGTAG[A/C]CTAAAAGTAAGCATG | 11622 |
rs245096272 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35512730 | TCTCAAATCTGAAAG[-/A]AAAAAAAAATCAAGA | 11622 |
rs245249439 | in-del | -/TAAAA | | | intron-variant | Ahr | GRCm38.p3 | 12:35503530 | TTTAAGAAAATTATT[-/TAAAA]TAATTTATTATTCAT | 11622 |
rs245417686 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35532507 | GCTCCGTATAAAACA[A/G]CTATACCTTAAAGGG | 11622 |
rs245670809 | snp | C/T | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499270 | TCTTTATCTTAATGC[C/T]AACGTAAAAGCTTCA | 11622 |
rs245685587 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35532652 | AAGCTTGGTGACCTG[A/G]TTGTTAAGGGTGAAC | 11622 |
rs245742177 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529667 | GGAAACACAACGGCA[A/G]AAATCCTGTCTTTCA | 11622 |
rs245798438 | snp | A/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536004 | GGTGATGCTGGACAT[A/G]AAGAGATAGAGATGA | 11622 |
rs245833020 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35517036 | TCTACTGAATAATTC[A/C]ACTGCTTCCTACCTT | 11622 |
rs245948288 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35502612 | GCCTGGAAGTGGAAA[C/T]TGTGGACTGTTCTGA | 11622 |
rs246037353 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533847 | AATAGCCCATGGAAA[C/T]AAAGACCAAAGCCTG | 11622 |
rs246063885 | snp | A/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536980 | CCCTGTGGGTACTGC[A/T]AAAGAACTGCCAGGA | 11622 |
rs246073131 | snp | G/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536613 | AAGGAGAAGAGGGGA[G/T]CCTGTGGGAGCAAGC | 11622 |
rs246114374 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35515966 | TAAACTGGTCTCCTA[C/T]TAATCAAGACTAAAA | 11622 |
rs246115607 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35528080 | CACTAGGTGAAGCCA[A/G]GGCAACCCTGAAGAA | 11622 |
rs246133075 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35527066 | ATACCAAACACTGCC[-/A]AAAAATACCAAGAAA | 11622 |
rs246182744 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35534473 | GGATTTTTTTTTTTT[A/T]AACGCATTGGTTGAG | 11622 |
rs246194023 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35513894 | CACAGGGAAGAAATA[C/T]TGGACCCTAGCAAGC | 11622 |
rs246223610 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35509034 | TATCAGCAAAAACAA[C/T]TGTCAGAAATAATAC | 11622 |
rs246234836 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35516558 | GGAACCAAGACTCAG[A/G]GCAGGTTTAAAAGGC | 11622 |
rs246351798 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524728 | GAATCACTATTGTCA[A/G]ACTCTGTACGCTACA | 11622 |
rs246405291 | snp | C/T | | | utr-variant-5-prime | Ahr | Mm_Celera | 12:35534641 | TGCCCGCGCCCTGCC[C/T]GCTCCACCTGCGTCC | 11622 |
rs246435047 | in-del | -/TG | | | intron-variant | Ahr | Mm_Celera | 12:35509720 | GTTTATGTGTGTGTA[-/TG]TGTGTGTGCATAAGC | 11622 |
rs246592550 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35505067 | GAAGAAAAGGTAAAA[A/C]GCACTAAAGCTGAGC | 11622 |
rs246757786 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35520169 | CATTGGATCCCCAGA[C/G]ACACTTGTGAGCCCT | 11622 |
rs246777904 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35525657 | TTTAAAGCTGTCGAA[G/T]TCTATATAACTTTGA | 11622 |
rs246785665 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35523279 | CAACCTTTAAAAATT[C/T]GCTCTGGGCACAATG | 11622 |
rs246880902 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35514614 | AGGTCTATGGTTGCT[-/G]GGGGGAAAAAAACCT | 11622 |
rs247283703 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35527244 | CATGCATTTGGCTTT[A/T]GAAATTGTAATGCTG | 11622 |
rs247293178 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35521104 | ACTCCACTAAGAGCT[A/C]GTATGAGCTCGTTAG | 11622 |
rs247457110 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35514070 | TGCTGGAGGAAGTCA[A/G]TCACTAGGGGGTTAT | 11622 |
rs247505685 | in-del | -/AG | | | intron-variant | Ahr | Mm_Celera | 12:35531739 | TCACAACGTTTTAAT[-/AG]AGTGAAGGGCTTCTA | 11622 |
rs247574256 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35526600 | TTTTTTTTTTTTTTT[G/T]TCTTGTCACCAACAT | 11622 |
rs247637664 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35532786 | CAAGCTGGTGACCTT[C/T]AAGGCATTTGAAGGC | 11622 |
rs247638848 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35526271 | TTAAAGTCATGCAAG[C/G]CAACACATTAAGTGG | 11622 |
rs247683532 | in-del | -/ACTA | | | intron-variant | Ahr | Mm_Celera | 12:35507252 | TTGCCACCAAGCCTG[-/ACTA]ACTGAGGTTGATCCT | 11622 |
rs247908509 | in-del | -/AAAAG | | | intron-variant | Ahr | GRCm38.p3 | 12:35508421 | GGTAGGGGTGGTTAT[-/AAAAG]AAAATTCCCAAGGCT | 11622 |
rs247992793 | in-del | -/GGAGAA | | | intron-variant | Ahr | Mm_Celera | 12:35528653 | GACCTGGAGGGGGTT[-/GGAGAA]GGAATGAATATGATC | 11622 |
rs248039429 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35516384 | TCAGCATCTAGATAC[A/T]TGGTTTATTTTTGTA | 11622 |
rs248161100 | in-del | -/C | | | utr-variant-3-prime | Ahr | GRCm38.p3 | 12:35500109 | CAACAACAACAACAA[-/C]AAAAAGTGAGGCACT | 11622 |
rs248174614 | snp | G/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536655 | AGTGGGGGAAGGAAT[G/T]GGGGGGGGGCGTCCA | 11622 |
rs248183195 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35521154 | AGTGTAGCATCACTT[C/T]CACAGACGAGTTCAT | 11622 |
rs248268471 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35507652 | TTTTAGTTTTTTTTT[A/T]AAATTTTCTTGCTTA | 11622 |
rs248333001 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531204 | TGCTTTCCTAGTTTA[A/G]TTGTAAGAACAGCAG | 11622 |
rs248469867 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35507799 | CTAAAAACATGGCTG[C/G]CTCAGACTGTACTTT | 11622 |
rs248506937 | in-del | -/TATTC | | | intron-variant | Ahr | Mm_Celera | 12:35503041 | CATGGATGCTCTCTA[-/TATTC]TATAATGTCCTTCAG | 11622 |
rs248522336 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529497 | GACCAAACCTATTCT[A/G]TAGGGAGGCAAGCAA | 11622 |
rs248534244 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35528786 | TGACTCTGGCCTCCG[A/C]GTGCATTTGCATACA | 11622 |
rs248565348 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35533756 | ATGCATCAATACAGA[C/T]AACTCCTAAATGGAA | 11622 |
rs248672165 | in-del | -/AAAAA | | | intron-variant | Ahr | Mm_Celera | 12:35503232 | CTTCATTCTCCATTC[-/AAAAA]AAAAAAAAAAAAGTC | 11622 |
rs248698331 | in-del | -/CAGTACAGTACAATA | | | intron-variant | Ahr | GRCm38.p3 | 12:35506428 | CACCAAACCCTCCAT[-/CAGTACAGTACAATA]CAGTACAGTACAGTA | 11622 |
rs248710020 | snp | A/G | | | utr-variant-5-prime | Ahr | Mm_Celera | 12:35534825 | GTCAGGAGGGGCCGC[A/G]GTGCTCTAGGGCTTC | 11622 |
rs248800990 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35528389 | AGGGTTTGTGCCTAG[A/C]CTTATTGCAATTTCT | 11622 |
rs248885044 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35526286 | GCAACACATTAAGTG[A/G]GTATTGGAGATTTGA | 11622 |
rs248897118 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35525650 | ACATTAATTTAAAGC[C/T]GTCGAAGTCTATATA | 11622 |
rs249076434 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35518925 | AAGAGGAATGCTGTC[A/C]CTTGAGATGAATTAT | 11622 |
rs249550396 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35503298 | TAAAAAGCAACCAGG[A/T]CTGTGATTTAAGCCA | 11622 |
rs249633989 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35513762 | GTCCAACGTCTCCCC[A/T]GAGACGCAAGGTAAT | 11622 |
rs249665904 | in-del | -/C | | | intron-variant | Ahr | Mm_Celera | 12:35524327 | GGCACAGCAGTGGTG[-/C]TGCACAGTGACACAG | 11622 |
rs249767682 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35506627 | TCCTCTCCTGGCACC[C/T]AAGTTCACCTGTACT | 11622 |
rs250016707 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35527177 | AAGAGCCTTTAAGTT[-/A]AAAAAAAAAACGATT | 11622 |
rs250167297 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35529133 | ACGTCTACCTGGAAG[C/T]CCCACCGAGTCAGAC | 11622 |
rs250199181 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35517277 | TGTGCTCCCAGTGTG[C/G]AGGGATGTGCTCCCA | 11622 |
rs250278653 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525130 | GCACACAACAGTTTG[A/G]GGTCTTGCTATTAAT | 11622 |
rs250280070 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35518959 | GAGTATAAAATAAAA[G/T]GCAGCTTACACAGGA | 11622 |
rs250470765 | snp | C/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536804 | TAACAATGGCATGAA[C/T]CACCAGAAAGAAATT | 11622 |
rs250566844 | in-del | -/A/AAA | | | intron-variant | Ahr | Mm_Celera | 12:35531396 | AAAATATATTGTATG[-/A/AAA]AAAAAGAGAATTTTA | 11622 |
rs250606099 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35524643 | GGAATCACTACTGTA[A/T]GAGTCGCTGTACACT | 11622 |
rs250608896 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35529381 | GGCATGTTCTTTTTT[C/T]AGGATAATCAACTGG | 11622 |
rs250686433 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35524806 | CTGGAATGGCCACTA[-/T]AGGGCTCAGTGTACA | 11622 |
rs250757264 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35525085 | AAGGGGAGACTTCTG[A/C]ATCTCATTGTGATGC | 11622 |
rs250777965 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35515469 | ACAAAGTGAGACCGT[C/T]CTGCAAAGCTGTTGT | 11622 |
rs250864013 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35523234 | TAGCATTTTGTATGT[C/T]GGGATTTTTCCTTTC | 11622 |
rs251212153 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35516102 | TGCTGTAAGGCACTG[A/G]CTGCTTATAATGCCA | 11622 |
rs251216939 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524392 | GGAATCTTTTTAAAC[A/G]GACTGTTAAGTGTCT | 11622 |
rs251730317 | in-del | -/GCGGCG | | | cds-indel | Ahr | Mm_Celera | 12:35504436 | AAGTCAACCTCACCA[-/GCGGCG]GCAGCGGTGGAGTCA | 11622 |
rs251826481 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35521784 | AGGGGGTGGGCCTTA[C/T]TGAAGTAGCAGTGTC | 11622 |
rs252049360 | in-del | -/GT | | | intron-variant | Ahr | Mm_Celera | 12:35525855 | CATGTGTGACAGAGA[-/GT]GTGTGTGTGTGTGTG | 11622 |
rs252051064 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35514045 | GGTGGAGCTGTTTGA[A/G]GTGCGGCCTTGCTGG | 11622 |
rs252138072 | snp | G/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35508425 | GGGGTGGTTATAAAA[G/T]AAAATTCCCAAGGCT | 11622 |
rs252276106 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35524876 | ACAGAACGCTTTTGT[-/A]AAAAAAATTACACTT | 11622 |
rs252333449 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35529389 | CTTTTTTTAGGATAA[C/T]CAACTGGTAATTTAG | 11622 |
rs252479035 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35531360 | GCCTAGGAGGAGTTG[A/C]AGGAGGAGAAAGAAT | 11622 |
rs252592984 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35532313 | TCAAACTGATTTCCT[A/T]CTACAGATAACTGTC | 11622 |
rs252610266 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35531495 | CAGTTTGATGTGAGC[C/T]CTTGTGTTAGACACA | 11622 |
rs252664395 | in-del | -/GTGCCGCT | | | intron-variant | Ahr | GRCm38.p3 | 12:35506473 | CATCCCTGCAACCAA[-/GTGCCGCT]GTGGGGCTAAGGTGA | 11622 |
rs252714466 | snp | C/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536929 | CTGTGATCGAGAAGC[C/T]GTTTGCTATTGGACA | 11622 |
rs252903401 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35516969 | TCGTATAATGCAAGT[C/G]TCTGCACTAATACTC | 11622 |
rs253021854 | in-del | -/TCTC | | | intron-variant | Ahr | Mm_Celera | 12:35532558 | AGCACAGTCAACACT[-/TCTC]TGTGTTTTTTCCTGA | 11622 |
rs253082090 | in-del | -/AACTAACG | | | intron-variant | Ahr | Mm_Celera | 12:35522297 | ACTAACTAACTAACT[-/AACTAACG]AAAATCCTGTGGTTG | 11622 |
rs253197884 | in-del | -/GAAAAAGAAA | | | upstream-variant-2KB | Ahr | GRCm38.p3 | 12:35535636 | TAGAGCTGATGGGAG[-/GAAAAAGAAA]AAAAAAAAAAAAGAT | 11622 |
rs253224666 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35521946 | TCTGAAAGTAAGAAA[A/T]CTCCCAGTTAAACGC | 11622 |
rs253422059 | in-del | -/A | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35500217 | ACAAAAACAGAGGTT[-/A]AAAAATATAGGAAAT | 11622 |
rs253478885 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35509658 | TGTTTATATGGTAAA[C/G]ATCGTGTGTATGTGT | 11622 |
rs253533162 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35516722 | TCCACTGCAAGCAGA[C/T]CAGACACTATTTCTG | 11622 |
rs253559453 | in-del | -/GA | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535642 | TGATGGGAGGAAAAA[-/GA]AAAAAAAAAAAAAAG | 11622 |
rs253588689 | in-del | -/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35519031 | CCCTGGAAGCACTAC[-/T]AAAAACCTCATAAAC | 11622 |
rs254151974 | in-del | -/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535896 | GCCATGGGGATGAGA[-/G]AAAAGAGACAGCAGA | 11622 |
rs254181594 | in-del | -/CACG | | | intron-variant | Ahr | GRCm38.p3 | 12:35528851 | ACACACACACACACA[-/CACG]CACACACACGGTGGG | 11622 |
rs254260871 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35506440 | CATCAGTACAGTACA[A/G]TACAGTACAGTACAG | 11622 |
rs254364971 | in-del | -/C | | | intron-variant | Ahr | Mm_Celera | 12:35528301 | GGGAGTAAGGGGTGT[-/C]TCTGACTCTTTTGTC | 11622 |
rs254415205 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35524822 | AGGGCTCAGTGTACA[A/C]CCACATGAAATCGCT | 11622 |
rs254484785 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35519227 | TCCTGGACCATGTGA[C/G]AGTTCGTAGAAATGA | 11622 |
rs254484817 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525184 | AATATGATCCCTTAA[A/G]TAGCACATGCCTTAA | 11622 |
rs254575572 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35531332 | AAATGGTGTGGGGAG[A/G]GTAGAAGGGAGGGCC | 11622 |
rs254591743 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35519844 | ATGACTTAGCTAATT[C/T]GACAAAACACATAAA | 11622 |
rs254600417 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35519501 | GTAGCCATGCCCCAG[C/G]ACCCATGGCTCCAGT | 11622 |
rs254746246 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35530333 | GGTCTGTCCTATGGA[A/C]ATGACACATTTATAT | 11622 |
rs254790019 | in-del | -/TA | | | downstream-variant-500B | Ahr | Mm_Celera | 12:35497937 | GGGCTCTGTTTTCTC[-/TA]TAGAGACAGAAAGAA | 11622 |
rs254863315 | in-del | -/GAGAGAGAGAATGAGAGAGAGAGAGAGAGAGAGAGA | | | intron-variant | Ahr | GRCm38.p3 | 12:35526020 | TTTGTGTGCATGAGT[lengthTooLong]GAGAGAGAGAGAGAG | 11622 |
rs254894368 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35532433 | CACTTTACTCCAAAT[C/T]TTCACGGAACTGTAT | 11622 |
rs254955966 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35521260 | TCTATAGGACAGATG[A/C]GTAACTCACATGAGA | 11622 |
rs254962883 | snp | A/G | | | utr-variant-5-prime | Ahr | Mm_Celera | 12:35534973 | GGGGCACCGAGCGTC[A/G]AAGGGAGCGCACACA | 11622 |
rs254967253 | in-del | -/TCC | | | intron-variant | Ahr | GRCm38.p3 | 12:35529317 | TGATTCTGCGGTGAT[-/TCC]GAAAAGATTAGGGTG | 11622 |
rs254985336 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35502723 | TATTTTTTTCACTGC[C/T]GCACAATTACTCATA | 11622 |
rs255026031 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35527097 | TCCATAGCATTCATG[C/T]AAAAATATACTAAAA | 11622 |
rs255032290 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35506088 | CTTATCACTTTTGTC[-/T]TTTTTTTTCAACATT | 11622 |
rs255095624 | in-del | -/AC | | | intron-variant | Ahr | Mm_Celera | 12:35502301 | TTTAAATATTTAGGA[-/AC]ACACACACACACAGA | 11622 |
rs255175251 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35527720 | AGAGGAAGGAGTGTG[C/G]TCGACCCTAGTTGGG | 11622 |
rs255213580 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35515431 | GTTTACTGATAATGC[A/G]AAAGGGCGATCAAAA | 11622 |
rs255227277 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35509696 | TGAGTATGTGCACAC[A/G]CACATGTGTGTTTAT | 11622 |
rs255249188 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35529634 | CTTTCTGCAACTACC[C/G]CTCCTTCAGAAATAA | 11622 |
rs255421897 | in-del | -/A | | | intron-variant | Ahr | GRCm38.p3 | 12:35532712 | TTCTGTTCAGGGGGG[-/A]ACAACGTAAGTACTT | 11622 |
rs255506710 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35528028 | ATGGAAAGACACACA[C/T]CCAGGAGTCTTGGCC | 11622 |
rs255508290 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35506109 | TTTCAACATTTTTCA[G/T]CTTTGTCCTGCTCTT | 11622 |
rs255573213 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35505462 | CCAACAGTGTTTTTT[G/T]TTGTTGTTGTTGTTG | 11622 |
rs255606099 | in-del | -/TTG | | | intron-variant | Ahr | Mm_Celera | 12:35528730 | TTTTTGGGGTTTTTT[-/TTG]TTTTGTTTTTTTAAA | 11622 |
rs255657352 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35514645 | ATAACATGTAAGTCA[C/T]GCATTGTTGCTCAAA | 11622 |
rs255836439 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35512784 | TTGACCTTACACTAT[-/A]AAAACAGATCAAGCA | 11622 |
rs255908063 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35530723 | TAGTTAAGAACATAA[A/G]GCTTTAGAGCCAACA | 11622 |
rs255936406 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35510108 | GCTTCTGTAGGAGGG[-/A]AAAGCACAGTCTACC | 11622 |
rs256072273 | in-del | -/AG | | | intron-variant | Ahr | Mm_Celera | 12:35509438 | CTCAAAACCAAAATA[-/AG]AGAGAGAGAGAGAGA | 11622 |
rs256255892 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35532024 | TGCTCAGCCATTTTC[A/C]TGAGACTGAATAACT | 11622 |
rs256607988 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35502835 | CATCTGTTATTTGCA[A/T]GAAGAACCTTTGATT | 11622 |
rs256690409 | in-del | -/CC | | | intron-variant | Ahr | Mm_Celera | 12:35529132 | ACGTCTACCTGGAAG[-/CC]TCCCACCGAGTCAGA | 11622 |
rs256693749 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35516882 | CTCGCACTTTTCAAG[C/G]CTGACCGAATCATTT | 11622 |
rs256730582 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35534006 | CTTAATGATTTAAAA[A/T]TTTACAGACCCAAAA | 11622 |
rs256757059 | in-del | -/C | | | intron-variant | Ahr | Mm_Celera | 12:35526982 | GTAATTCTCAATAAA[-/C]CCCTCTACTATACTG | 11622 |
rs256768170 | in-del | -/GC | | | intron-variant | Ahr | GRCm38.p3 | 12:35534325 | CTAAAGCTCACGGCA[-/GC]GGAGATCTAGAGTGG | 11622 |
rs256815455 | in-del | -/TT | | | intron-variant | Ahr | Mm_Celera | 12:35506087 | CTTATCACTTTTGTC[-/TT]TTTTTTTTTCAACAT | 11622 |
rs256816408 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35523424 | TCAACAAAGTTTCCA[A/G]CTAGGTCTTATGTAC | 11622 |
rs256867179 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35527750 | GATGTTTACAACAGT[A/G]CCTTCCCCTCATGGC | 11622 |
rs256966070 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35519516 | CACCCATGGCTCCAG[G/T]CTGAACTCAACTGAC | 11622 |
rs257014836 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35508119 | AATTATGAGTGAAAA[A/T]GTTCCCTTACTTGGC | 11622 |
rs257131300 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35533377 | ACGACATTTGCGTCC[-/T]TTTAAAGTGTACCAA | 11622 |
rs257147999 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35513414 | GACTGAATTATAAAG[A/C]TATTAAAACTTTTAT | 11622 |
rs257314119 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35514291 | GGATTCTAACCCCCC[A/G]GTACTGTAAGCCCAA | 11622 |
rs257977144 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35534014 | TTTAAAATTTTACAG[A/G]CCCAAAAGCACTCCA | 11622 |
rs257979916 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35500758 | AGACCTTAAAAACGA[A/C]TTTTAGTCTGTTAGA | 11622 |
rs258073894 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35524015 | GGCAGGAGCTCAAGG[G/T]TACAGTCCACAGCAG | 11622 |
rs258154861 | in-del | -/GGTGGTGGT | | | intron-variant | Ahr | GRCm38.p3 | 12:35524116 | CCGGAGACTATGGGC[-/GGTGGTGGT]GGTGGTGGTGGTGGT | 11622 |
rs258161906 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529535 | ACGCTGCTCAGTGAT[A/G]TAGGTGGTTTAGCAA | 11622 |
rs258186558 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35518849 | GGACGACCCACCTAT[C/T]TATCCCACAATTCTT | 11622 |
rs258272407 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35532749 | AAGGACCTAAGTGCC[A/T]GCACTAAAGTCTTCG | 11622 |
rs258305729 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35529351 | AATGTTTCATCTTCC[-/T]ATTTCTTAAGCAGAG | 11622 |
rs258312655 | in-del | -/ACACT | | | intron-variant | Ahr | Mm_Celera | 12:35522546 | ACGGCTTCAAACCTC[-/ACACT]ACACTACCTAAAACA | 11622 |
rs258410851 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35521377 | CACAGAAGAGGTAAC[A/G]GCCGTGTGACACAGA | 11622 |
rs258666213 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35502621 | TGGAAACTGTGGACT[A/G]TTCTGAGCTCCCATG | 11622 |
rs258697223 | snp | A/G | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536913 | GAGGTAGAAACTGGA[A/G]CTGTGATCGAGAAGC | 11622 |
rs258775346 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35525495 | GTGCACGGTAAAGCA[C/T]AGGGGGCTCCCTGGC | 11622 |
rs258805492 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35530587 | GACTGAGTCCTGAAA[C/T]GGCAGTCAACTGTTT | 11622 |
rs258891745 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525363 | TAAATTATGTTAGAA[A/G]ATTAATTTCAAACAG | 11622 |
rs259203332 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518778 | GTGAGTAGGGATATG[C/T]TCCCAGTGTGCAGGG | 11622 |
rs259316171 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35510798 | CTGAGGTTGTGACCT[C/T]TGGCCTCCACACATG | 11622 |
rs259319699 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35519077 | CCATTCCCTCATCTT[C/T]AAATGGAGAGCACTG | 11622 |
rs259625554 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35514312 | GTAAGCCCAAGTACA[A/C]GCTCCCTTCTGCAAG | 11622 |
rs259650933 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35528310 | GGGTGTCTCTGACTC[-/T]TTTGTCTGCACTTGG | 11622 |
rs259709442 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35515423 | TTGAGCCTGTTTACT[A/G]ATAATGCGAAAGGGC | 11622 |
rs259745400 | snp | A/C | | | utr-variant-3-prime | Ahr | GRCm38.p3 | 12:35500109 | CAACAACAACAACAA[A/C]AAAAAGTGAGGCACT | 11622 |
rs259863947 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35529162 | ACTCTTGCCAGTGTC[C/T]TGTTGCTGCTCTCTG | 11622 |
rs259941280 | snp | A/G | | | utr-variant-5-prime | Ahr | Mm_Celera | 12:35534817 | TCCCGAGGGTCAGGA[A/G]GGGCCGCAGTGCTCT | 11622 |
rs260375331 | in-del | -/AAACAAAG | | | intron-variant | Ahr | Mm_Celera | 12:35510500 | CCAGTGTTGGTTTAA[-/AAACAAAG]AAACAAAGAAAGAAA | 11622 |
rs260453862 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35513934 | AACAGGGCAAACGCC[A/G]GATCCTCTAGCTGTG | 11622 |
rs260507835 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35523789 | CATAAACTTTATTTT[G/T]CATACACACAAACAA | 11622 |
rs260573689 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35517293 | AGGGATGTGCTCCCA[C/G]TATGCAGGGATGTGT | 11622 |
rs260669480 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35529173 | TGTCTTGTTGCTGCT[C/T]TCTGGCTGTGATGGA | 11622 |
rs260672077 | in-del | -/C | | | intron-variant | Ahr | Mm_Celera | 12:35519378 | AAGATAAGGATAGTA[-/C]CAATGCCATGGTGTT | 11622 |
rs260781708 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529565 | AGTGTTCCTAGAGAC[A/G]CGGGTGTTAAACAGA | 11622 |
rs260878263 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35521433 | GATTGGCATACCGGG[A/C]GGTGGGCCTTACCTG | 11622 |
rs260936060 | in-del | -/TTT | | | intron-variant | Ahr | Mm_Celera | 12:35533683 | TCCTAAAATAATTTA[-/TTT]TTTTAAAAAAATAAC | 11622 |
rs260989178 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35525788 | GTGTCAAAGAGAGAT[A/T]GAAATGGGGAGAGGG | 11622 |
rs260989351 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35520206 | GGTACTGGGAATCAA[A/G]CCTGGGTCTTCCAGA | 11622 |
rs261097945 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35526363 | AGCCAGCCCCAGTCC[G/T]AGCCCCAATCAGTCT | 11622 |
rs261270079 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35507808 | TGGCTGGCTCAGACT[A/G]TACTTTAGAGACAGG | 11622 |
rs261374218 | snp | C/T | | | missense | Ahr | Mm_Celera | 12:35504711 | GGCTGTCTAACAGCG[C/T]AGGGCTTGAAGGAGG | 11622 |
rs261546742 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35531655 | GGCCCCATACTGTAG[A/C]TCTGCGGAAAATTTA | 11622 |
rs261585229 | snp | C/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536744 | TATTAGAAACAAATT[C/T]AAGAGTTAAAATTGA | 11622 |
rs261592657 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35531231 | GCAGTGGAGGAGACT[G/T]CCCTGCTAGTAAAAA | 11622 |
rs261646795 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35533315 | AAAATACTAAAGCAC[A/T]GAAAGCCAGGGTCCA | 11622 |
rs261723300 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35515473 | AGTGAGACCGTCCTG[C/T]AAAGCTGTTGTGAAG | 11622 |
rs261809298 | in-del | -/ACTTAG | | | intron-variant | Ahr | Mm_Celera | 12:35533103 | TAAGGAAAATCAGTT[-/ACTTAG]ACTTAGACACTCAAG | 11622 |
rs261815545 | in-del | -/GTGTGT | | | intron-variant | Ahr | Mm_Celera | 12:35509634 | ATGTGGTGTATATGG[-/GTGTGT]GTGTGTTTATATGGT | 11622 |
rs262116702 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35513312 | TCTTTAGGGAGCACA[A/G]AAGGAAAAACCCACT | 11622 |
rs262119748 | in-del | -/TA | | | intron-variant | Ahr | Mm_Celera | 12:35519993 | CTAAAGGAAGTTTTC[-/TA]TATAGATTGAGAAAC | 11622 |
rs262144608 | snp | G/T | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536506 | TTGATTTTTACACAT[G/T]TTGAAACTAGGAAAG | 11622 |
rs262198769 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35533116 | TTACTTAGACTTAGA[A/C]ACTCAAGCGGAGCTC | 11622 |
rs262406712 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35503554 | TTATTATTCATACTA[G/T]TTTAAGTAAACTATA | 11622 |
rs262514898 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35509574 | ATATGAGTTTATGTG[A/G]TATATGTGGTGTGTG | 11622 |
rs262516070 | in-del | -/AAG | | | intron-variant | Ahr | Mm_Celera | 12:35532082 | CCAAAGAGAATAAGC[-/AAG]AACAGGATTTAAGTG | 11622 |
rs262701494 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529653 | CTTCAGAAATAAAGG[A/G]AAACACAACGGCAGA | 11622 |
rs262739085 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35528854 | cacacacacacacac[A/G]cacacacacGGTGGG | 11622 |
rs262801034 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35534474 | GATTTTTTTTTTTTT[A/T]ACGCATTGGTTGAGA | 11622 |
rs262867604 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35528111 | AACTGGGAGGATTGT[A/G]GGAGCCAGAGGGGTC | 11622 |
rs262943565 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35508994 | GGTACTGGGAATGCC[A/G]TCTCAGATTACAACT | 11622 |
rs263031964 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35533574 | TAAATCTTAAGTTGG[-/T]TTTTTTTGTTGTTTT | 11622 |
rs263063044 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35525675 | TATATAACTTTGAAA[A/G]GCTAAATGAATAAAT | 11622 |
rs263144396 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35526945 | CGTCCCCTCAGGGAC[C/T]GCTCTACCGACGAAA | 11622 |
rs263236774 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35524681 | ACATGGAATCACTAC[C/T]GTATGAGTAGGTGTT | 11622 |
rs263533331 | in-del | -/AGACCCG | | | utr-variant-3-prime | Ahr | Mm_Celera | 12:35499546 | CACAAACAGGATTAC[-/AGACCCG]AGACAGTTTTTCAAA | 11622 |
rs263545890 | in-del | -/AAAAA | | | intron-variant | Ahr | Mm_Celera | 12:35527126 | ACCACTGAGCTGTCC[-/AAAAA]AAAAAAAAAAAAAAA | 11622 |
rs263564082 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35527765 | GCCTTCCCCTCATGG[C/G]TCAGGGATCTATGTG | 11622 |
rs263601787 | snp | C/T | | | downstream-variant-500B | Ahr | Mm_Celera | 12:35497854 | TTTAAGTAACCCTTT[C/T]ATGAAAGACTTGGTG | 11622 |
rs263823577 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35527311 | TAAGCACAGATTCTC[A/C]AATTTCCACTTCCTT | 11622 |
rs263941606 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35524063 | TCCTACGGGGCCAGT[A/G]TCTTTAACAAGCCCC | 11622 |
rs264083988 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35519949 | AAATCAGTTTATATG[-/A]AATGAATAAATTTCC | 11622 |
rs264378126 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35513712 | ATTGCCTGAAACTTT[A/G]AATCAAAAAGCTCTT | 11622 |
rs264476957 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35519449 | CATAGTGGAAAGAAC[G/T]GGCTTTACTCCATGG | 11622 |
rs264503335 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35516385 | CAGCATCTAGATACT[C/T]GGTTTATTTTTGTAC | 11622 |
rs264639277 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35522695 | TAAGAAGATCGATTC[-/A]ATGCCGTATTATTTG | 11622 |
rs264744126 | in-del | -/GAA | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35536132 | GCCCAGGCTGTGGAG[-/GAA]GAAGAACCCGCATCA | 11622 |
rs264813033 | snp | A/C | | | intron-variant | Ahr | Mm_Celera | 12:35530656 | GGCAATGCCCAGGAC[A/C]GGGGCCATCATGCAC | 11622 |
rs264905191 | snp | C/G | | | intron-variant | Ahr | Mm_Celera | 12:35517314 | AGGGATGTGTTCCAA[C/G]TGTGCAGGGATGTGC | 11622 |
rs264975837 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35527144 | AAAAAAAAAAAAAAA[A/T]AGGTATTTTCATACT | 11622 |
rs265278999 | snp | G/T | | | intron-variant | Ahr | Mm_Celera | 12:35523952 | GAGTGAAGTGGATCT[G/T]GTGCAGCAGGAATCA | 11622 |
rs265317185 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35510747 | GAAAACTCTTGTTTC[-/A]AAAAAACAAGGCGGA | 11622 |
rs265333743 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35529071 | TAAGTTCAGCTTGAC[A/G]TTCTAACTCCCTAGA | 11622 |
rs265445545 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35525327 | GCATGTAAAAGATAA[C/T]TAAGGAATTACTATG | 11622 |
rs265496931 | in-del | -/TT | | | intron-variant | Ahr | Mm_Celera | 12:35528724 | CATTACTTTTTGGGG[-/TT]TTTTTTGTTTTGTTT | 11622 |
rs265637935 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35521660 | CTTTGTATTATGCTA[C/T]GGCTACAAGCCTATG | 11622 |
rs265703173 | in-del | -/TGTGTG | | | intron-variant | Ahr | GRCm38.p3 | 12:35509710 | GCACATGTGTGTTTA[-/TGTGTG]TGTGTGTGTATGTGT | 11622 |
rs265850425 | in-del | -/ACAC/CG | | | intron-variant | Ahr | GRCm38.p3 | 12:35528853 | ACACACACACACACA[-/ACAC/CG]CACACACACGGTGGG | 11622 |
rs265904268 | in-del | -/CTT | | | intron-variant | Ahr | Mm_Celera | 12:35510708 | TCCCAGCAGCCTACC[-/CTT]CTTGGTGATCTCCTG | 11622 |
rs265915637 | snp | C/T | | | intron-variant | Ahr | Mm_Celera | 12:35519151 | AAATAGTTCAAACAT[C/T]AAGAGGCACTTCACA | 11622 |
rs265918724 | snp | A/T | | | intron-variant | Ahr | Mm_Celera | 12:35524736 | ATTGTCAGACTCTGT[A/T]CGCTACAAACCACAC | 11622 |
rs266063654 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35500851 | TTCAAATCACACAGA[-/G]GAAACGCTCACACAC | 11622 |
rs266079210 | snp | A/G | | | intron-variant | Ahr | Mm_Celera | 12:35520061 | TTCTGCATATGACAT[A/G]TATTCTTTTTAAAAT | 11622 |
rs266186248 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35534457 | AGGTGCCTGAAAGCA[-/G]GGATTTTTTTTTTTT | 11622 |
rs266239039 | in-del | -/AAAC | | | intron-variant | Ahr | Mm_Celera | 12:35515444 | GCGAAAGGGCGATCA[-/AAAC]AAACACACAAAGTGA | 11622 |
rs386835480 | in-del | -/GT | | | intron-variant | Ahr | Mm_Celera | 12:35514164 | TGTGTGTGTGTGTGT[-/GT]TTGTGTGTGTGTGTG | 11622 |
rs386888297 | in-del | -/TTT | | | intron-variant | Ahr | Mm_Celera | 12:35526597 | TTTTTTTTTTTTTTT[-/TTT]GTCTTGTCACCAACA | 11622 |
rs386907488 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518427 | AGGGATGTGCTCCCA[C/G]TGTGCAGGGATGTGT | 11622 |
rs386918593 | in-del | -/GAAAA | | | intron-variant | Ahr | GRCm38.p3 | 12:35508425 | GGGGTGGTTATAAAA[-/GAAAA]TTCCCAAGGCTCAGA | 11622 |
rs386935885 | in-del | -/AA | | | upstream-variant-2KB | Ahr | GRCm38.p3 | 12:35535643 | GATGGGAGGAAAAAG[-/AA]AAAAAAAAAAAAAGA | 11622 |
rs386982869 | in-del | -/CT | | | intron-variant | Ahr | Mm_Celera | 12:35529151 | ACCGAGTCAGACTCT[-/CT]TGCCAGTGTCTTGTT | 11622 |
rs386987036 | in-del | -/GAA | | | intron-variant | Ahr | GRCm38.p3 | 12:35507934 | GAAGCTAAAAATTAA[-/GAA]ATATTTTTACAAAAT | 11622 |
rs386987691 | in-del | -/CTCT | | | intron-variant | Ahr | Mm_Celera | 12:35532559 | GCACAGTCAACACTT[-/CTCT]GTGTTTTTTCCTGAA | 11622 |
rs387006206 | in-del | -/TGAGAAGAAATTATTT | | | intron-variant | Ahr | Mm_Celera | 12:35519700 | TGGCATGATACATTT[-/TGAGAAGAAATTATTT]ATTCTTAACCACTGC | 11622 |
rs387044211 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35530536 | GACTCTAAGAAAAAA[-/A]GACATGAATACAAAA | 11622 |
rs387068699 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35533581 | TAAGTTGGTTTTTTT[-/T]GTTGTTTTTGTTTTC | 11622 |
rs387122782 | in-del | -/G | | | utr-variant-5-prime | Ahr | Mm_Celera | 12:35534752 | CAGAGGAGACTCGGG[-/G]CTGCCCGAGCTGGCC | 11622 |
rs387135678 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35507655 | TAGTTTTTTTTTTAA[-/A]TTTTCTTGCTTATGG | 11622 |
rs387145530 | in-del | -/GT | | | intron-variant | Ahr | Mm_Celera | 12:35525872 | TGTGTGTGTGTGTGT[-/GT]CACAGAAAGAGTGTG | 11622 |
rs387161710 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35517466 | TGTGCTCCCAGTGTG[C/G]AGGGATGTGTTCCAA | 11622 |
rs387188387 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35506096 | TTTTGTCTTTTTTTT[-/T]CAACATTTTTCATCT | 11622 |
rs387195314 | in-del | -/CACACACACACACAAACA | | | intron-variant | Ahr | Mm_Celera | 12:35523208 | ACACACACACACACA[-/CACACACACACACAAACA]AAACCTTCCTTAGCA | 11622 |
rs387211514 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35527187 | AGTTAAAAAAAAAAA[-/A]CGATTTTAAAGCAAA | 11622 |
rs387237743 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35503682 | AGATGCTTAGGCCTA[C/T]AAGGTTTTTTCAGCT | 11622 |
rs387242078 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518432 | TGTGCTCCCACTGTG[C/G]AGGGATGTGTTCCAA | 11622 |
rs387262865 | in-del | -/ACG | | | intron-variant | Ahr | Mm_Celera | 12:35509174 | ACTTCTTACAGGACG[-/ACG]CCTCCTATCAGATGC | 11622 |
rs387271765 | in-del | -/CAAAAAAAAAAAAAAAAAAAAAAAA | | | intron-variant | Ahr | Mm_Celera | 12:35533882 | CTCTGTCAGAATTGG[-/CAAAAAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 11622 |
rs387312363 | in-del | -/CAAAA | | | intron-variant | Ahr | Mm_Celera | 12:35531279 | TAAAACAAAACAAAA[-/CAAAA]ACTTGACCAGGAAAG | 11622 |
rs387314617 | in-del | -/CCT | | | intron-variant | Ahr | GRCm38.p3 | 12:35529318 | TGATTCTGCGGTGAT[-/CCT]GAAAAGATTAGGGTG | 11622 |
rs387355701 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35508119 | AATTATGAGTGAAAA[-/A]GTTCCCTTACTTGGC | 11622 |
rs387371770 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35517382 | TGTGCTCCCAGTGTG[C/G]AGGGATGTGCTCCCA | 11622 |
rs387378849 | in-del | -/CAAAGAAA | | | intron-variant | Ahr | Mm_Celera | 12:35510511 | TTAAAAACAAAGAAA[-/CAAAGAAA]GAAACAAAAGAAAAC | 11622 |
rs387444436 | in-del | -/G | | | intron-variant | Ahr | Mm_Celera | 12:35534459 | GTGCCTGAAAGCAGG[-/G]ATTTTTTTTTTTTTA | 11622 |
rs387470785 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35528724 | CATTACTTTTTGGGG[-/T]TTTTTTTGTTTTGTT | 11622 |
rs387502959 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35520803 | TCTAGACTTAGGAAA[-/A]TAATTTAGAAATCTC | 11622 |
rs387525198 | in-del | -/TGCGTTCTCCCATATAA | | | intron-variant | Ahr | Mm_Celera | 12:35507841 | TGTCATTTATTCTAA[-/TGCGTTCTCCCATATAA]AAGGTGGGAAAATTA | 11622 |
rs387525701 | in-del | -/TGG | | | intron-variant | Ahr | Mm_Celera | 12:35524166 | TGGTGGTGGTGGTGG[-/TGG]GACAGGCCTTCATCC | 11622 |
rs387526276 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35513624 | GTTAATGTTTTTTTT[-/T]CAAGGTCAGTGTGAA | 11622 |
rs387538611 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518485 | TGTGCAGGGATGTGT[A/T]CCAAGTGTGCAGGGA | 11622 |
rs387553070 | in-del | -/AAA | | | upstream-variant-2KB | Ahr | Mm_Celera | 12:35535655 | AAGAAAAAAAAAAAA[-/AAA]GATAATCTAGGAACA | 11622 |
rs387564201 | in-del | -/AATAA | | | intron-variant | Ahr | GRCm38.p3 | 12:35503533 | AAGAAAATTATTTAA[-/AATAA]TTTATTATTCATACT | 11622 |
rs387569151 | in-del | -/T | | | intron-variant | Ahr | Mm_Celera | 12:35532568 | AACACTTGTGTTTTT[-/T]CCTGAAATTGAGGTA | 11622 |
rs387592755 | in-del | -/GAGAGA | | | intron-variant | Ahr | Mm_Celera | 12:35526084 | AGAGAGAGAGAGAGA[-/GAGAGA]AGGGTACAAGTGCAC | 11622 |
rs387594868 | in-del | -/C | | | intron-variant | Ahr | Mm_Celera | 12:35530125 | ACAGTCACAATATAC[-/C]AGCTCAACCATTCCC | 11622 |
rs387645731 | in-del | -/ACACACAC | | | intron-variant | Ahr | Mm_Celera | 12:35502542 | CACACACACACACAC[-/ACACACAC]GTGCATGTGCAACAC | 11622 |
rs387688232 | in-del | -/ATACAGTACA | | | intron-variant | Ahr | GRCm38.p3 | 12:35506440 | CATCAGTACAGTACA[-/ATACAGTACA]GTACAGTACATCCCT | 11622 |
rs387688951 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35534475 | TTTTTTTTTTTTTAA[-/A]CGCATTGGTTGAGAC | 11622 |
rs387689550 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35517487 | TGTGTTCCAAGTGTG[A/C]AGGGATGTGCTCCCA | 11622 |
rs387705545 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35510109 | CTTCTGTAGGAGGGA[-/A]AAGCACAGTCTACCT | 11622 |
rs387719303 | in-del | -/A | | | intron-variant | Ahr | GRCm38.p3 | 12:35510753 | TCTTGTTTCAAAAAA[-/A]CAAGGCGGAAGGTTT | 11622 |
rs387782918 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35524822 | AGGGCTCAGTGTACA[-/A]CCACATGAAATCGCT | 11622 |
rs387787777 | in-del | -/GAGAGAGAGAGACAGACAGA | | | intron-variant | Ahr | Mm_Celera | 12:35509457 | AGAGAGAGAGAGAGA[-/GAGAGAGAGAGACAGACAGA]CAGACAGACAGACAG | 11622 |
rs387791827 | in-del | -/AG | | | intron-variant | Ahr | Mm_Celera | 12:35531741 | ACAACGTTTTAATAG[-/AG]TGAAGGGCTTCTATA | 11622 |
rs387803405 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35508343 | ATTGCCTTAAAAAAA[-/A]TATGTCATTAAAATT | 11622 |
rs387814399 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35532713 | TCTGTTCAGGGGGGA[-/A]CAACGTAAGTACTTT | 11622 |
rs387863070 | in-del | -/A | | | intron-variant | Ahr | Mm_Celera | 12:35518982 | ACACAGGAGCAGTAA[-/A]GGCCAGACGTGATAA | 11622 |
rs578360399 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518728 | TGCTCCCACTATGCA[C/G]GGATGTGCTCCCAGT | 11622 |
rs578382714 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35528864 | CACACGCACACACAC[A/G]GTGGGGGAATAATTT | 11622 |
rs578544697 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518766 | GATGTGCTCCCAGTG[A/T]GTAGGGATATGCTCC | 11622 |
rs578749406 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35533810 | TTTCTGAGGGGGGAA[A/G]AAAAATCTCCCATCT | 11622 |
rs578919271 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35523971 | CAGCAGGAATCACAA[C/T]CTATGAGCCAGGTTC | 11622 |
rs578935107 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518275 | CTGTGCAGGGATGTG[C/T]TCCCAGTGTGCAGGA | 11622 |
rs578973058 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35530570 | GGAGATGGGCTGGCA[C/T]AGACTGAGTCCTGAA | 11622 |
rs578975701 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35502547 | CACACACACACGTGC[A/G]TGTGCAACACAAGTA | 11622 |
rs579104136 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35515459 | AAACAAACACACAAA[A/G]TGAGACCGTCCTGCA | 11622 |
rs579131422 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518334 | CCCAGTGTGCAGGGA[C/T]GTGCTCCCAGTGTGC | 11622 |
rs579139676 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35527189 | GTTAAAAAAAAAAAC[A/G]ATTTTAAAGCAAATT | 11622 |
rs579170257 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35533575 | TAAATCTTAAGTTGG[C/T]TTTTTTGTTGTTTTT | 11622 |
rs579292971 | snp | A/G | | | upstream-variant-2KB | Ahr | GRCm38.p3 | 12:35536643 | CAGAGCAGCAGGAGT[A/G]GGGGAAGGAATGGGG | 11622 |
rs579340022 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35517060 | CTACCTTTAGAATGT[C/T]TCTACTCACTCGGTA | 11622 |
rs579351335 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518694 | CTGTGCAGGGATGTG[C/T]TCCCAGTGTGCAGGG | 11622 |
rs579540122 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35517348 | CACTGTGCAGGGATG[C/T]GTTCCCAGTGTGCAG | 11622 |
rs579554666 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35519027 | CATGCCCTGGAAGCA[C/T]TACTAAAAACCTCAT | 11622 |
rs579729654 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35528933 | TCCATTTGTTCCCCC[A/C]GCTCTGGTGCAAGGG | 11622 |
rs579769992 | snp | G/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35519793 | TATTATGACAAGAAA[G/T]TTAAATTCCTTGACA | 11622 |
rs579972273 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35524336 | AGTGGTGTGCACAGT[A/G]ACACAGAGTGAAGGG | 11622 |
rs580085942 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35524692 | CTACCGTATGAGTAG[C/G]TGTTCACTATAGACC | 11622 |
rs580190955 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35533928 | AAAAAAAAAGCAAGG[A/G]GAAATGAACTACAGG | 11622 |
rs580197079 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518557 | ATGTGCTCCCAGTGT[A/G]CAGGGATGTGCTCCC | 11622 |
rs580260961 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518595 | AGGGATGTGCTCCCA[C/G]TGTGCAGGGATGTGT | 11622 |
rs580333540 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35506097 | TTTGTCTTTTTTTTT[A/C]AACATTTTTCATCTT | 11622 |
rs580359914 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35524118 | GGAGACTATGGGCGG[C/T]GGTGGTGGTGGTGGT | 11622 |
rs580484433 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518787 | GATATGCTCCCAGTG[A/T]GCAGGGATGTGCTCC | 11622 |
rs580605139 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35529305 | GGTCTAGAAATAATG[A/C]TTCTGCGGTGATCCT | 11622 |
rs580639854 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35529333 | CCTGAAAAGATTAGG[A/G]TGAATGTTTCATCTT | 11622 |
rs580707399 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35517634 | TGTGCTCCCAGTGTG[C/G]AGGGATGTGCTCCCA | 11622 |
rs580838032 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35517986 | AGGGATGTGCTCCCA[C/G]TGTGCAGGGATGTGC | 11622 |
rs581046897 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35514150 | TCCCCACCCCCTTCT[C/G]TGTGTGTGTGTGTGT | 11622 |
rs581143156 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518637 | AGGGATGTGCTCCCA[C/G]TGTGCAGGGATGTGC | 11622 |
rs581372891 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35518656 | GCAGGGATGTGCTCC[A/C]AGTGTGCAGGGATGT | 11622 |
rs581433243 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35518698 | GCAGGGATGTGCTCC[A/C]AGTGTGCAGGGATGT | 11622 |
rs581609739 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35524871 | CACTGACAGAACGCT[A/T]TTGTAAAAAAAATTA | 11622 |
rs581624092 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35530472 | GAACAACATGCAGTT[A/G]TTCAAAGTGCTTCAC | 11622 |
rs581703648 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35520007 | CTATATAGATTGAGA[A/T]ACAAGATACATTTTA | 11622 |
rs581755278 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518286 | TGTGTTCCCAGTGTG[C/G]AGGAATGTGCTCCCA | 11622 |
rs581783955 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35531256 | TAAAAACAAAAAACA[A/G]AACAAAATAAAACAA | 11622 |
rs581808646 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35533808 | CTTTTCTGAGGGGGG[A/G]AAAAAAATCTCCCAT | 11622 |
rs582014246 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35524166 | TGGTGGTGGTGGTGG[C/T]GGGACAGGCCTTCAT | 11622 |
rs582128749 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35533811 | TTCTGAGGGGGGAAA[A/G]AAAATCTCCCATCTC | 11622 |
rs582198874 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35523815 | AACAAATCAACATTC[A/G]TCGTAAAGGCACAAG | 11622 |
rs582203813 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35517350 | CTGTGCAGGGATGTG[C/T]TCCCAGTGTGCAGGG | 11622 |
rs582226754 | snp | A/C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518495 | TGTGTACCAAGTGTG[A/C/G]AGGGATGTGCTCCCA | 11622 |
rs582334878 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35528867 | ACGCACACACACGGT[A/G]GGGGAATAATTTCAA | 11622 |
rs582348314 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35527262 | AATTGTAATGCTGAG[A/T]GACTTACCTAGTTAA | 11622 |
rs582400967 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518745 | GATGTGCTCCCAGTG[A/T]GTAGGGATGTGCTCC | 11622 |
rs582568663 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518788 | ATATGCTCCCAGTGT[A/G]CAGGGATGTGCTCCC | 11622 |
rs582746006 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35503417 | TATATCTTCAAATAA[A/G]CTAATATTTGTAAAG | 11622 |
rs582748490 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35533807 | TCTTTTCTGAGGGGG[A/G]AAAAAAAATCTCCCA | 11622 |
rs582766624 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35517329 | GTGTGCAGGGATGTG[C/T]TCCCACTGTGCAGGG | 11622 |
rs582780561 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35517711 | GGAGGGATGTGCTCC[C/T]AGTGTGCAGGGATGT | 11622 |
rs582891499 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35524002 | AGGCTATGAAGTTGG[C/T]AGGAGCTCAAGGTTA | 11622 |
rs583155868 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35524685 | GGAATCACTACCGTA[A/T]GAGTAGGTGTTCACT | 11622 |
rs583300640 | snp | G/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35509483 | GACAGACAGACAGAG[G/T]TGTATGTATGTTATA | 11622 |
rs583408157 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518641 | ATGTGCTCCCAGTGT[A/G]CAGGGATGTGCTCCC | 11622 |
rs583534844 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35524696 | CGTATGAGTAGGTGT[A/T]CACTATAGACCACAT | 11622 |
rs583735087 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35519887 | TGTGTGTGTATAATA[A/G]AATGGCTTAAGAAAC | 11622 |
rs583788397 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35517409 | CCCACTGTGCAGGGA[C/T]GTGCTCCCAGTGTGC | 11622 |
rs583795633 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518600 | TGTGCTCCCAGTGTG[C/G]AGGGATGTGTTCCAA | 11622 |
rs583978318 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35529327 | GGTGATCCTGAAAAG[A/C]TTAGGGTGAATGTTT | 11622 |
rs584182944 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518578 | ATGTGCTCCCAGTGT[A/G]CAGGGATGTGCTCCC | 11622 |
rs584218148 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35523119 | CCCACACACACTTTC[C/T]ATTAAACCCTATGTC | 11622 |
rs584287468 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35526966 | ACCGACGAAACATGA[A/C]GTAATTCTCAATAAA | 11622 |
rs584329993 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518723 | GGATGTGCTCCCACT[A/G]TGCACGGATGTGCTC | 11622 |
rs584392801 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35525027 | TGAGGAGGTGCTGCC[C/T]GGTGACCTGGATGGC | 11622 |
rs584511120 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35514620 | TATGGTTGCTGGGGG[A/G]AAAAAACCTATAACA | 11622 |
rs584679628 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35502544 | ACACACACACACACG[C/T]GCATGTGCAACACAA | 11622 |
rs584740479 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35527682 | ACACACCCACAAGTG[A/G]CAAACGTGCAGCAAG | 11622 |
rs584819656 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35517050 | CCACTGCTTCCTACC[C/T]TTAGAATGTCTCTAC | 11622 |
rs584827160 | snp | G/T | | | upstream-variant-2KB | Ahr | GRCm38.p3 | 12:35536144 | GAGGAAGAAGAACCC[G/T]CATCACTGTGGGTGG | 11622 |
rs584834542 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518663 | TGTGCTCCCAGTGTG[C/G]AGGGATGTGCTCCCA | 11622 |
rs584850424 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35521425 | CAAAGTCAGATTGGC[A/C]TACCGGGAGGTGGGC | 11622 |
rs584912375 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35523844 | AGCACTGAAATGTAC[A/G]ATGATTCAAGTCAAT | 11622 |
rs585010384 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518251 | CCAGTGTGGAGGGAT[A/G]TGCTCCCACTGTGCA | 11622 |
rs585041940 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35530568 | CAGGAGATGGGCTGG[C/T]ACAGACTGAGTCCTG | 11622 |
rs585252379 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518290 | TTCCCAGTGTGCAGG[A/G]ATGTGCTCCCACTGT | 11622 |
rs585330508 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35533809 | TTTTCTGAGGGGGGA[A/G]AAAAAATCTCCCATC | 11622 |
rs585427566 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35528918 | CACCCAACTCTTAAT[C/T]CCATTTGTTCCCCCA | 11622 |
rs585482264 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35524170 | GGTGGTGGTGGTGGG[A/G]CAGGCCTTCATCCCA | 11622 |
rs585537319 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518789 | TATGCTCCCAGTGTG[C/T]AGGGATGTGCTCCCA | 11622 |
rs585641602 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35517335 | AGGGATGTGCTCCCA[C/G]TGTGCAGGGATGTGT | 11622 |
rs585673118 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35528768 | AAGCAAGTGAAGAAG[A/T]CTTGACTCTGGCCTC | 11622 |
rs585755231 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35517361 | TGTGTTCCCAGTGTG[C/G]AGGGATGTGCTCCCA | 11622 |
rs585782930 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518763 | AGGGATGTGCTCCCA[C/G]TGAGTAGGGATATGC | 11622 |
rs585961109 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35524004 | GCTATGAAGTTGGCA[C/G]GAGCTCAAGGTTACA | 11622 |
rs585998873 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35529139 | ACCTGGAAGTCCCAC[C/T]GAGTCAGACTCTTGC | 11622 |
rs586007053 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35517430 | CCCAGTGTGCAGGGA[C/T]GTGCTCCCAGTGTGG | 11622 |
rs586189032 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35533812 | TCTGAGGGGGGAAAA[A/G]AAATCTCCCATCTCA | 11622 |
rs586191291 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518524 | CACTGTGCAGGGATG[C/T]GTTCCAAGTGTGCAG | 11622 |
rs586341217 | snp | C/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35518579 | TGTGCTCCCAGTGTG[C/G]AGGGATGTGCTCCCA | 11622 |
rs586580700 | snp | A/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35526055 | GAGAGAGAGAGAGAG[A/T]GAGAGAGAGAGAGAG | 11622 |
rs586754829 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35529329 | TGATCCTGAAAAGAT[C/T]AGGGTGAATGTTTCA | 11622 |
rs586760602 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35517600 | CACTGTGCAGGGATG[C/T]GTTCCAAGTGTGCAG | 11622 |
rs586766943 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35519939 | AAAATAACTCCAAAT[C/T]AGTTTATATGAATGA | 11622 |
rs586785226 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35521426 | AAAGTCAGATTGGCA[C/T]ACCGGGAGGTGGGCC | 11622 |
rs586966761 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35517948 | ATGTGCTCCCAGTGT[A/G]CAGGGATGTGCTCCC | 11622 |
rs587097658 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35519713 | TTTGAGAAGAAATTA[C/T]TTATTCTTAACCACT | 11622 |
rs587329677 | snp | C/G/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518768 | TGTGCTCCCAGTGAG[C/G/T]AGGGATATGCTCCCA | 11622 |
rs587335928 | snp | A/C | | | intron-variant | Ahr | GRCm38.p3 | 12:35524690 | CACTACCGTATGAGT[A/C]GGTGTTCACTATAGA | 11622 |
rs587423358 | snp | C/T | | | intron-variant | Ahr | GRCm38.p3 | 12:35518652 | GTGTGCAGGGATGTG[C/T]TCCCAGTGTGCAGGG | 11622 |
rs587448211 | snp | A/G | | | intron-variant | Ahr | GRCm38.p3 | 12:35524701 | GAGTAGGTGTTCACT[A/G]TAGACCACATGGAAT | 11622 |
rs864257276 | snp | C/T | | | missense | Ahr | GRCm38.p3 | 12:35508170 | AGTCTAGCTTGTGTT[C/T]GGTCCTGAAGATGAA | 11622 |
rs864303867 | in-del | -/A | | | utr-variant-3-prime | Ahr | GRCm38.p3 | 12:35499051 | TCTCATCAGCTTTTT[-/A]TATAACATATGAAAA | 11622 |