SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3718577 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Stac | Mm_Celera | 9:111563030 | TGACTCCCTGGAGAC[G/T]CAGTGTAAGGGCAGA | 20840 |
rs3719690 | snp | C/T | 0.235537 | 0.249581 | intron-variant | Stac | Mm_Celera | 9:111563169 | AAATAAGCATAAGCA[C/T]CTCTCATATTCCAGA | 20840 |
rs29590874 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Stac | GRCm38.p3 | 9:111659030 | CCAGTTAATCTGTTC[C/T]GTGCTTCTCATCTCC | 20840 |
rs29591650 | snp | G/T | 0.188366 | 0.242283 | utr-variant-3-prime | Stac | Mm_Celera | 9:111562057 | AGGACGCCCTCGTTC[G/T]CGATCTGTAGGTAAG | 20840 |
rs29604604 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Stac | GRCm38.p3 | 9:111568620 | ATATCATCGCTATTC[C/T]CTTTCTTCCCTCATC | 20840 |
rs29639594 | snp | A/G | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Stac, Gm36088 | Mm_Celera | 9:111579392 | TCTCTCTCTGTCTCT[A/G]TCTGTCTGTCTCTGT | 20840 |
rs29640551 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Stac | GRCm38.p3 | 9:111562000 | CTGCTGGACTCTGTG[C/T]CTTGGACCTTGCCCT | 20840 |
rs29641278 | snp | A/C | 0.42 | 0.183303 | intron-variant | Stac | GRCm38.p3 | 9:111657810 | TCACAGATACCATTA[A/C]ACTTGCACATTGTGT | 20840 |
rs29644688 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Stac | GRCm38.p3 | 9:111655924 | ATCAACTGAACAAAG[A/G]ATGGCTTGCTGGAAA | 20840 |
rs29686029 | snp | C/T | 0.255 | 0.24995 | intron-variant | Stac | Mm_Celera | 9:111563725 | GACCCTTCTTTAAAA[C/T]GGGGTGAGGCTATTT | 20840 |
rs29687176 | snp | C/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111643034 | ACCAGCATGTGCTTG[C/G]TCTTCCCAAGTCTGA | 20840 |
rs29694790 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111680589 | GGACTTATATTTCCA[C/T]GCCACCAATCATTAT | 20840 |
rs29704607 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111630420 | GCTCAAAGGCACACA[A/G]TACTGCTTGCTTCAC | 20840 |
rs29740886 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111657867 | TTGTTTTTGAGACAG[A/G]GTTTCTCTGTGTATC | 20840 |
rs29786244 | snp | C/G | 0.42 | 0.183303 | intron-variant | Stac | Mm_Celera | 9:111630444 | GCTTCACTCACATTT[C/G]TATGCAAGGTTGGGT | 20840 |
rs29787724 | snp | A/T | 0.345679 | 0.230967 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111572881 | TTATATTGTTTAGTA[A/T]TTATTAAAGCCAGTC | 20840 |
rs29790945 | snp | C/T | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111567406 | AGAATCAATTTTCTC[C/T]GACCTCTCTGTTAAT | 20840 |
rs29829417 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111686346 | GAGGGACCAAACTTG[A/G]AACTTCATGTTTGCC | 20840 |
rs29832210 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Stac | GRCm38.p3 | 9:111630988 | AATCCACAAGGAGAG[A/G]AAGCCAGCTCAGTAG | 20840 |
rs29840071 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111681566 | CAGTCATTACCCAGC[C/T]TTGGTCTGTACTTTA | 20840 |
rs29893423 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Stac | Mm_Celera | 9:111562610 | CGCTGGCCTCCTGCT[C/T]GGGAAGGGACTGCTA | 20840 |
rs29894639 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111680690 | GTTGCTTCCTTGCTT[A/G]CTTCCAGTACCTTGT | 20840 |
rs29894870 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111630434 | AATACTGCTTGCTTC[A/G]CTCACATTTGTATGC | 20840 |
rs29931056 | snp | A/C | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111642932 | GGGCATCCTGAGAGC[A/C]CATGGAGAATTTAGC | 20840 |
rs29976442 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Stac | GRCm38.p3 | 9:111659233 | TTTGCCCAGATACTG[C/T]CAATCGAATGTTCAT | 20840 |
rs29991570 | snp | G/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111686148 | GAGTACACCCCCAGG[G/T]GTAGGTCATCCTCCG | 20840 |
rs30029242 | snp | G/T | 0.18 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111656382 | ACTTCCTGAGGGTCA[G/T]GTAGGGTCTTTCTGT | 20840 |
rs30035713 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Stac | GRCm38.p3 | 9:111691170 | TGAATACTAGACTCC[C/T]TCCTTATTTTTATGT | 20840 |
rs30037404 | snp | C/T | 0.18 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111563757 | AGGACTTAATTTCTT[C/T]GCAACTCTCTTTTCC | 20840 |
rs30043201 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Stac | Mm_Celera | 9:111632921 | TGCTTGAGGTGTCCT[A/G]AGAACCCCACTAAGG | 20840 |
rs30076591 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Stac | Mm_Celera | 9:111630628 | TTCTGGACACCAAAA[G/T]ACTATTGCATCCACT | 20840 |
rs30090389 | snp | A/C | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111573063 | ACTGTCTGTAGCTTC[A/C]GGTCCAGAGGATCTG | 20840 |
rs30090664 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Stac | Mm_Celera | 9:111659559 | ACAATACAGACAATG[A/C]ATTTTACATCTGGAT | 20840 |
rs30092135 | snp | A/G/T | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111568803 | CAGAGGCCCATGCTT[A/G/T]TACTCTTGCCCGGCG | 20840 |
rs30127106 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Stac | GRCm38.p3 | 9:111631165 | TCTTGAGTGGTGGTG[A/G]TGATGATGATGGTGG | 20840 |
rs30130381 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Stac | Mm_Celera | 9:111683899 | ACTGGTACTCTATGC[A/G]TACGTGTGTCGATTG | 20840 |
rs30135725 | snp | A/G | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111568877 | ACTCTATTTTGTAAA[A/G]TAGAAATACTGCATG | 20840 |
rs30137197 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Stac | GRCm38.p3 | 9:111630956 | GACTGGCTGGAGGGC[A/G]AGGCTTAGATCTGCT | 20840 |
rs30169579 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Stac | Mm_Celera | 9:111567374 | ATGTTATAAAAAAAA[A/C]CACGGCATTCATTTT | 20840 |
rs30173635 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111680581 | TCTTGTTTGGACTTA[A/C/T]ATTTCCATGCCACCA | 20840 |
rs30177252 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111664105 | AATTTTTGGGGTCAC[C/T]TATATATACTATCAT | 20840 |
rs30182024 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Stac | Mm_Celera | 9:111655347 | GCTTAAAGTGGCTTC[A/G]CTCAGCACCTGGGGG | 20840 |
rs30229969 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111636565 | CAGCTTTGAGGTGGG[C/T]TCCTTTGGTTAAGTA | 20840 |
rs30232189 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111616901 | ATCTATCTATCTATC[C/T]ATCCATCCATCCATC | 20840 |
rs30277978 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111630717 | GGGGCTCACAGCAAG[A/G]TTTTTGTTTGTTTGT | 20840 |
rs30321940 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Stac | Mm_Celera | 9:111581793 | CAAACCTAGTCCCGA[G/T]AGACTTCTCAGAGTG | 20840 |
rs30423144 | snp | G/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111643086 | CCCGCACAGGCAGCA[G/T]CCTGCGAGGCATACA | 20840 |
rs30425218 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111658261 | TGGGTTTTCCATCTT[C/T]ATTTGCTGCTAAGCA | 20840 |
rs30431581 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111604362 | GAACTTGATACTTGG[A/G]GAACTTGATACCAAC | 20840 |
rs30468189 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Stac | GRCm38.p3 | 9:111562469 | CTGCTCTCAGGACGC[C/T]TTGATGTGCTGTGCA | 20840 |
rs30477832 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111685106 | GGGACGTCATGTCAG[C/T]AACTTACTCTTCTTT | 20840 |
rs30477861 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Stac | GRCm38.p3 | 9:111635286 | GTGAGCAGGGAGAGG[C/T]TCCACATGACCCATT | 20840 |
rs30482498 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Stac | Mm_Celera | 9:111659723 | ATCTCTTAGTCACGT[A/G]CACTATTAATGTCAA | 20840 |
rs30518159 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111635336 | CCTTGCTTTCTTAGG[C/T]CCCACCAATGTGCTG | 20840 |
rs30519269 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Stac | Mm_Celera | 9:111658195 | CAACATGCATTTGAA[A/G]GGAAAGACAAAGATC | 20840 |
rs30761993 | snp | A/T | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111668876 | GTGGAAAACCCTGTG[A/T]CTGGAAAAGCCTAGA | 20840 |
rs30820134 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Stac | GRCm38.p3 | 9:111671225 | AGTGATGGATATGGC[A/G]CTTAAATATCCCTTG | 20840 |
rs30858310 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111677263 | TGCGAGGAATAGAGC[A/G]GGGGAGGTGATTCTG | 20840 |
rs30874687 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111668895 | AAACCTGGAATTCAC[A/G]TGAGTGGAAAACCCT | 20840 |
rs30960812 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111677438 | TTCTGTAGGACATTG[C/T]GTCAAGTAGAAGAAG | 20840 |
rs30973803 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Stac | GRCm38.p3 | 9:111672477 | TATTAGGGGGGCGGT[A/G]TATGTGTTTGGTATA | 20840 |
rs31014394 | snp | C/T | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111672623 | AAACAAAACCCACCC[C/T]CACCAAAAATCCAAC | 20840 |
rs33630412 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111564213 | GTTATAGGAATGGAA[C/T]GTTATGTACGCTGCC | 20840 |
rs33644814 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | Mm_Celera | 9:111632868 | TCAGATAAAATCACA[A/G]CACAACCTTCTTTAG | 20840 |
rs33644821 | snp | A/G | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111651969 | AAAGCTGGGGGGAGC[A/G]TACAATAGAGACATA | 20840 |
rs33648891 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Stac | GRCm38.p3 | 9:111630981 | TCTGCTCAATCCACA[A/G]GGAGAGGAAGCCAGC | 20840 |
rs33655573 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111642913 | ATTAGGAAGCACAGA[C/T]ATTGGGCATCCTGAG | 20840 |
rs33656426 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111565015 | TCAGCTCCTGCTTGA[C/G]TTCCAGTCCTGACTT | 20840 |
rs33658602 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111568536 | GCCTCTACCTCCCAA[A/G]CACTGAGGTGCCAGA | 20840 |
rs33661759 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111631163 | AATCTTGAGTGGTGG[C/T]GGTGATGATGATGGT | 20840 |
rs33676918 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Stac | Mm_Celera | 9:111658043 | AAAAAAATCCACATG[C/T]TAGGTATCAGGGTGG | 20840 |
rs33702092 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Stac | GRCm38.p3 | 9:111653318 | ATGAGTGAATGTTAC[A/G]ATTTTTTTAAAAAAG | 20840 |
rs33702690 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111633186 | TGAGCATGGAGCATG[A/C]CGGGACCCCCTCTGG | 20840 |
rs33739020 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111630905 | CCCCAGCACCCCCAC[C/T]ATCACCCCAATAGAC | 20840 |
rs33740926 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Stac | GRCm38.p3 | 9:111635252 | GGACTCAGTAGTTCA[C/T]CCTGTATCCCATAAG | 20840 |
rs33748344 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Stac | Mm_Celera | 9:111642850 | CCAGCTGGGATTTTA[A/G]CAGTGGTCTACACAG | 20840 |
rs33750397 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Stac | Mm_Celera | 9:111692208 | AATAGGATTAGCGAT[C/T]GATAATGATGTCTTC | 20840 |
rs33752617 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Stac | Mm_Celera | 9:111630691 | CCTGCAGAAGATGTA[G/T]GGATAGGAATGGGGC | 20840 |
rs33767311 | snp | C/G | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111681729 | AAAGAGGAGCATCAA[C/G]AAACTGGACCACGTG | 20840 |
rs33776067 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Stac | Mm_Celera | 9:111567410 | TCAATTTTCTCTGAC[C/T]TCTCTGTTAATGGCC | 20840 |
rs45646585 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111627855 | TTATCAAAGCTGATC[G/T]CGTCTTTGAGGAATT | 20840 |
rs45649217 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111606099 | GATGGGGTTTGGGCA[C/T]AGAAGTGGCTCCCTA | 20840 |
rs45654564 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111634263 | CATGAACCATTGACT[C/T]ATAGTATCGGGGTAG | 20840 |
rs45656925 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111630467 | GGTTGGGTTGTCTAT[A/C]ATAGCTTGAATAGGT | 20840 |
rs45662770 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111655097 | GCTGATGTCTGACGG[C/T]GAAATGTTGGGTTGG | 20840 |
rs45674404 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641085 | CCAGAGGTCTGAGAT[A/G]CTCATTTAAAATTCA | 20840 |
rs45674864 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111642468 | TCCTAGCTGCCTGGA[C/T]GTAAGTCTTCTCCTG | 20840 |
rs45676138 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111685615 | AAAACACCTGGAATG[A/G]ATGCTCTCTTCTGTT | 20840 |
rs45679354 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Stac | GRCm38.p3 | 9:111643623 | GACACACCCAAGGCT[A/C]GTGGGCAGACACAGT | 20840 |
rs45681747 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | Mm_Celera | 9:111636484 | TCAGCCCTTAGCACC[C/T]GCCTTTCTGCCACCC | 20840 |
rs45691125 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111583087 | TCAAACAAGAGACAA[A/C]TCCCTGAGAAAACAT | 20840 |
rs45697149 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111629565 | TAAAAATGTAAAAGC[A/G]TGTAATAAAAAATGG | 20840 |
rs45707689 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111610340 | ATAGGAAGTGTAGAC[A/G]TGAGTTTAATATTTA | 20840 |
rs45710372 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111671178 | TGCTGCCTTGTGGTT[A/G]ATGCTCTGTTCCTAG | 20840 |
rs45711323 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111674423 | TCTTTTCATTTTCTC[A/G]AAGTCACTTTGGAAG | 20840 |
rs45719633 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111609110 | GGTCTGGTCGGACCT[C/T]GATCTGCTACACCTG | 20840 |
rs45728575 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111630969 | GCGAGGCTTAGATCT[C/G]CTCAATCCACAGGGA | 20840 |
rs45737768 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111684991 | GACTACACACGCTTA[C/T]AGGAATTGGCTCTGA | 20840 |
rs45739527 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111660533 | TGTGGGAAGAGAGAA[A/G]AAGGATCTTGTTGAA | 20840 |
rs45744730 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111673996 | ACACGGAAGCAGAAG[C/T]GAATCTGTGTCCCTC | 20840 |
rs45758462 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Stac | GRCm38.p3 | 9:111687108 | TGGTGCTGCTCTTGC[C/T]GTGACCTTGGCCAGG | 20840 |
rs45768846 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111676306 | CCCTTTAAAAGGAGG[G/T]CTGTAGCTGCAGGTA | 20840 |
rs45772048 | snp | A/C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111639292 | CCAATATCTACCCTA[A/C/T]CAAGGAACTGCTACA | 20840 |
rs45777959 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Stac | GRCm38.p3 | 9:111635443 | GGTATGAACTCCTGG[A/G]TACCAAGGCTGTGTG | 20840 |
rs45778852 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111680291 | AATGTTACATGAGAT[A/C]TGTAGAACCCACAAT | 20840 |
rs45778926 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111575938 | CCAAACTCTCAGAGC[A/T]CCCCTACACTTCATG | 20840 |
rs45779668 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111627433 | CTGAGTCAGAATCTC[A/T]TACTGGTTTGGAGCT | 20840 |
rs45788056 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Stac, Gm36034 | GRCm38.p3 | 9:111594204 | ATTCTGTCTTGAAGA[C/T]TAAGGCATTCAATTT | 20840 |
rs45819881 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Stac | Mm_Celera | 9:111583816 | AAAACCATATAGGTT[A/G]TTTCTACTGATTAAA | 20840 |
rs45823188 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111625726 | CTTGCACTAAAAAAT[A/G]GTTGTCTTTTGTAAG | 20840 |
rs45844817 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Stac | Mm_Celera | 9:111614710 | GAGTTAGTGGAGTGA[C/T]ATTTTTGAGAATTCC | 20840 |
rs45845166 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111632321 | TAGACTTCCTTGTTC[C/T]TGAGTTTAGATTGTG | 20840 |
rs45846580 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111656183 | AGAGCTGCCTCTCCA[G/T]CCACTCTCATCCTGT | 20840 |
rs45861750 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111581691 | TTAGATAGATGAGAG[A/T]CACAGCTTGACCTGT | 20840 |
rs45870338 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641100 | GCTCATTTAAAATTC[A/G]GGGGGACTGAAAATG | 20840 |
rs45878450 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111629579 | CATGTAATAAAAAAT[A/G]GGAAGATAGGAGAAT | 20840 |
rs45901737 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Stac | Mm_Celera | 9:111633782 | GAGCAGAAAGGCAAC[C/T]CATGAGGCTGCAAGC | 20840 |
rs45906209 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111639370 | AGTGAGATGCCAGTA[A/T]TTATTGAGTGGCAGA | 20840 |
rs45916909 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111625400 | GAAGAACCATGCAAC[C/T]ACCATGTCAAAAATT | 20840 |
rs45922780 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Stac | GRCm38.p3 | 9:111638173 | CTCATGAAAAGCAGG[C/T]TCAACGTTAGCCTGC | 20840 |
rs45924628 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111570291 | TTCTTGGTTGCTATG[C/T]AGTTCAGCCTAGCTT | 20840 |
rs45932501 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111622930 | AGGTGTACATTGTTG[A/G]AGGAAGTCTGCACTG | 20840 |
rs45932989 | snp | A/C | | | intron-variant | Stac | GRCm38.p3 | 9:111687642 | GGAGGGGAGAACTGA[A/C]TCCTGCAACTTGTTT | 20840 |
rs45940311 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111639253 | CCCCTCAGGCTCAGA[C/T]CCAGGGCTTTGAATT | 20840 |
rs45942095 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111632028 | GTGTGATTAGAAGTT[A/C]AAAATTACCCTAATT | 20840 |
rs45942238 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111629111 | TTCCTCCCAAGGGCA[C/T]GCCTACAACTGAGCA | 20840 |
rs45946106 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111627163 | TTGGAGGAATTGAAA[G/T]GTCCTCTAAGTCATG | 20840 |
rs45950823 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111636312 | CTGGCTGGGTAAAAC[A/G]CTAGGCTCGGTCCCT | 20840 |
rs45951780 | snp | G/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111616408 | AGCATGAGAACCCTT[G/T]GTGGTATCGAATGTG | 20840 |
rs45954482 | snp | C/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111634028 | ATCTTTAGTTTCCCA[C/G]TCATTAATAACCCAC | 20840 |
rs45971668 | snp | A/T | | | intron-variant | Stac | Mm_Celera | 9:111645965 | GTACCTCCGAATGTG[A/T]CTATGTTTGGAGATC | 20840 |
rs45976125 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111636486 | AGCCCTTAGCACCCG[C/T]CTTTCTGCCACCCAG | 20840 |
rs45989970 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111576714 | TCTCAAACCTTCTCA[A/C]CTTGGACATGGTGTT | 20840 |
rs45995723 | snp | C/T | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111571218 | ACAGAAGGACACCCT[C/T]GCTGTGCTGGAGGGA | 20840 |
rs45997703 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111669392 | ATGATTCAGAAAGGT[A/G]GGAGCTTTTTTTTTC | 20840 |
rs46001563 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111566766 | TGAATTCAGTTCAAA[A/G]CGCATCGCACATTGA | 20840 |
rs46015748 | snp | C/T | | | upstream-variant-2KB | Stac | Mm_Celera | 9:111690747 | AATACACTTGGTGTA[C/T]GGACACCTGGTCCCC | 20840 |
rs46015950 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111658662 | TTCATTTCCTATGTG[C/T]ACAGATGTGTGCAGT | 20840 |
rs46020525 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111638379 | GGTGTGTGTGGGTGG[A/T]CACCGTGTCAGGCAA | 20840 |
rs46023775 | snp | C/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111573944 | AGAGCAGATTAGATT[C/T]CTGTGTTCACTTTGT | 20840 |
rs46025933 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111634720 | AAGCTCAGAGCTGGT[C/T]TATGGGTCCCCTGAA | 20840 |
rs46027372 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111670966 | GGCTCTGTGACTGGG[A/G]TTTGACTGAAGTAAA | 20840 |
rs46029650 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111577014 | TTCTCCTGTGCCCTG[A/G]GTGGATAAAGGTTCT | 20840 |
rs46030228 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111622076 | CAACTTGGGAAGTTT[G/T]TATTTTCCCAAGAGG | 20840 |
rs46031527 | snp | C/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111633537 | ATGACAAGTCTGGGT[C/G]TCTGGCTTCAGGAAA | 20840 |
rs46033052 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641862 | TGCTTATTGGATACA[A/G]ATCTTTCATGTGTGT | 20840 |
rs46053809 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111666481 | CCTAGGTGCCCATGT[C/G]ATGATCCCTGTGTCA | 20840 |
rs46057400 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Stac | Mm_Celera | 9:111629202 | GACAGTTATGAAAGC[C/T]ATTGATTCTTTCAAG | 20840 |
rs46068340 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111674812 | ATTTGAGTCAGGGAG[C/T]GAGAGGGAGATAATG | 20840 |
rs46080735 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111633495 | GGCACTTTGCATTCT[A/G]CCTCTTGTCTTTGCT | 20840 |
rs46089967 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Stac | GRCm38.p3 | 9:111569752 | TATGAGATTACTGTG[A/G]GCATTGCTGCAGCTC | 20840 |
rs46105158 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111634519 | CTCAGGCAGGTATAC[A/G]TGGGCCACATACAGA | 20840 |
rs46121428 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111636669 | GGCCAGGCTCCCTGA[A/G]GACAGTGAAGAAGAG | 20840 |
rs46145614 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111635560 | TTGACATTAATCTGG[C/T]TAAATGGTCTCCAGG | 20840 |
rs46148038 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Stac | Mm_Celera | 9:111635906 | GGTGTCCTTGCCCTG[C/G]TTTTCAGCCTCAGTA | 20840 |
rs46162067 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Stac | GRCm38.p3 | 9:111634126 | AACTTCCTCCATCCC[A/C]AAGGCTGAAGATGTC | 20840 |
rs46177407 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111649302 | ATTTCATTATGAAAA[C/T]ACCATACACATGAAT | 20840 |
rs46180258 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111628602 | TATCTTGAATGTATG[A/G]TAGTGTTTCCTCATG | 20840 |
rs46181647 | snp | A/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111573344 | CAATATCTCAAGCTA[A/T]GGGAAGGAGAGCACA | 20840 |
rs46181734 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111675023 | GGGTGTGGGCTGAAC[A/C]TGGTGTCCAAGGACT | 20840 |
rs46182512 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Stac | Mm_Celera | 9:111681518 | GGCCTTTACATGGGC[A/G]TGGCTGAACTGCTCA | 20840 |
rs46190002 | snp | A/C | | | intron-variant | Stac | GRCm38.p3 | 9:111640299 | TGTTCAACAGTGAGA[A/C]TGATCTCCCTAAGGT | 20840 |
rs46200069 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111605930 | AATTTAAGAGAAGGG[A/G]ACATTGCAAGCTAGA | 20840 |
rs46217996 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111671766 | TGGAAAGCAGATACA[C/T]AGGCTCAGGGAGCTC | 20840 |
rs46226883 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Stac | Mm_Celera | 9:111569507 | CATCGCTGTAGTCAC[A/T]GGGCTGAAAATGACT | 20840 |
rs46227096 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Stac | GRCm38.p3 | 9:111623535 | CATTGTGAACAAGCT[A/G]CAGAGATGATCTCCT | 20840 |
rs46239992 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Stac | GRCm38.p3 | 9:111635184 | CATGTATACCTGGGA[A/G]GTTCTGCCAGGCCCC | 20840 |
rs46244843 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Stac | Mm_Celera | 9:111665588 | TTGAGTGCACCCTCA[A/C]TCAGATTCATAAATC | 20840 |
rs46247216 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111673471 | ATCACCTGTTGCTCA[C/T]CTGTCTCCTCTATTT | 20840 |
rs46248211 | snp | C/T | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111609161 | GTTGTATGTGCCCCT[C/T]ATGCTTGACTAGCAA | 20840 |
rs46254877 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111685813 | TAGACCAGTGGGTCT[A/G]CTGTATCCTAGTTTC | 20840 |
rs46260154 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111640184 | CCTTGCAGGGAGGGC[A/G]TCATTCATCACTCAC | 20840 |
rs46261270 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111655425 | GTCCCAGATGTGGGA[G/T]AGTTAGTGGAAAATA | 20840 |
rs46263160 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111628941 | TTCCACCTTTCTCCC[A/T]TGACAGCCACGGCCA | 20840 |
rs46267777 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime | Stac | GRCm38.p3 | 9:111562012 | GTGCCTTGGACCTTG[C/G]CCTGCCACTTCGGAG | 20840 |
rs46270157 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111630539 | GAAATCACACTCTTT[A/T]CACCCAAGTCTCAGG | 20840 |
rs46279124 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Stac | Mm_Celera | 9:111634262 | TCATGAACCATTGAC[G/T]CATAGTATCGGGGTA | 20840 |
rs46279410 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111654783 | TAAAAGGGCAGAAAC[A/G]ACTGGTGCACACACA | 20840 |
rs46280465 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111626861 | CAGGACACAGGTCCT[C/T]GTGCGCATGTGACAT | 20840 |
rs46288650 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111581564 | CTGTTCCTTGATTTG[C/T]CAGTTCCCATCAGCA | 20840 |
rs46290871 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577227 | TTCTGAGAGCCTATG[A/G]CATTCAGGTCTTGAA | 20840 |
rs46300781 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111613840 | TAAGGAGGCAGGGAC[A/G]GGCCGTAGCTGGTAG | 20840 |
rs46301456 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111674944 | TTAGGGATGCTCATG[A/G]TTGAACATGCAGGGA | 20840 |
rs46303930 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111636584 | TTTGGTTAAGTATTC[A/C]TCTGGAGCCATTCTT | 20840 |
rs46314911 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111629758 | GCTTCACTTTAGTGA[A/C]AAAGTTGGATATGGT | 20840 |
rs46318561 | snp | A/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111618601 | CCATCACACCACACT[A/T]ACGTCAAGCAGACCC | 20840 |
rs46321076 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Stac | GRCm38.p3 | 9:111585964 | GACCAGACATCTTGG[C/T]TTTTAATGGCCTGCA | 20840 |
rs46323889 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111649173 | TTTTTCTGGCCCATC[A/G]ATAAGGATTATGATA | 20840 |
rs46327974 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Stac, Gm36034 | Mm_Celera | 9:111593531 | TATTCTGTGTTACTT[A/C]TTATGTGACATCACA | 20840 |
rs46329783 | snp | A/C | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111670394 | CTCAGCCAGGGCCTT[A/C]TTCCTGGTCTTCAGC | 20840 |
rs46333312 | snp | C/T | 0.124444 | 0.216185 | missense, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111572383 | CTGGAAAGAAACCAA[C/T]CCTGTCCTGAATCTT | 20840 |
rs46362217 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111607434 | TATATATCTGGGATG[C/T]TGTTCTGTGGATACT | 20840 |
rs46366530 | snp | A/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571241 | TGGAGGGACAGAAGG[A/T]CACCCTCTCTGTGCT | 20840 |
rs46371066 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111654857 | ACATTGGTGGGTTTC[A/G]GAATAAAATACAAAT | 20840 |
rs46374117 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111632083 | AGAAGATGGCCTAGT[C/T]GGCCATCGATGGGAA | 20840 |
rs46382890 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111633876 | CCCACTGAGAACCGC[C/T]CACTTGGGAACAGAA | 20840 |
rs46391013 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111624065 | CATTATTCCAAAAAT[G/T]TAGCCCAAACCACTG | 20840 |
rs46397424 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111688314 | GAACTCATCTCCATT[A/G]GCTAGGACGCCTAAG | 20840 |
rs46398029 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111634618 | AAACTAATTCTCCCT[C/T]CACCTAGCCCTGTTT | 20840 |
rs46398405 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111645363 | CTTTGAGGTATACTC[A/G]TGAGGGTTCATTATT | 20840 |
rs46398851 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111633938 | TCATAACACCCTCTG[A/T]GGCGGATTGATTAAA | 20840 |
rs46419180 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111632306 | TGGTGATAAATGCAT[C/T]AGACTTCCTTGTTCT | 20840 |
rs46424562 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111638459 | ACATTTCTTATTGAA[A/G]TGGACTGCTTGAAAG | 20840 |
rs46428972 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111627560 | TCCTCTCTACGTGGG[A/T]GCTAGGGACTGAAAT | 20840 |
rs46431334 | snp | C/T | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111615343 | ACTCTGGGATCACCA[C/T]TTCAGGTTCCTTAAA | 20840 |
rs46436966 | snp | C/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111634567 | CAGGCTTCTGGTGGA[C/G]GATGCCAGCTGCTGT | 20840 |
rs46437220 | snp | A/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111611461 | AAGGGCAGAAGGAAG[A/T]CAGGCAAGTGTAGTT | 20840 |
rs46440354 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111569791 | TTCTCCCTGTGCATA[G/T]ACTATTTTCATGAGT | 20840 |
rs46445198 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111656553 | GCAATGCTCTCACAC[C/T]GAGTAAGCCTCTCAT | 20840 |
rs46466745 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Stac | GRCm38.p3 | 9:111647313 | ACCACGAGGCCTAAA[C/G]CCAAAAGGTCTCATC | 20840 |
rs46471317 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111637502 | AAAAATGAAAGTTAT[A/G]TTATTTGAAAGAAAA | 20840 |
rs46510377 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111632707 | CAGGACCTGTTCCAT[C/T]AGGAGGCTCACAGCT | 20840 |
rs46511682 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111644513 | AGACCACACCTTGAT[G/T]TCACAAAGTAGTAAG | 20840 |
rs46514627 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111643207 | GCATCAGTACCACAC[C/T]GGCTTCATATCAGGA | 20840 |
rs46514881 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111657698 | AAAACAAAACAAAAC[A/C]AAACCAAACAACCTC | 20840 |
rs46517802 | snp | C/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111582977 | TTCAGTGTCCCTCTG[C/G]GGTGTGTTCTAGCAC | 20840 |
rs46528604 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111644861 | AAAGATGTGTTAGCT[A/C]TCCACATCTTTGTTT | 20840 |
rs46529079 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111640026 | TATCTTCTTATGTGC[A/G]GGACATGACCCATAC | 20840 |
rs46530293 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111636164 | CCTAGACCCCTAGCT[A/T]CTCAGGAGGCTGCAA | 20840 |
rs46531857 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111635946 | ATTTCTCTCTTGCCT[A/G]TGGGACTTATGGTGA | 20840 |
rs46549027 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111642971 | GACCTTAATGCAGAC[A/G]TGTTGATTCACCCAT | 20840 |
rs46549366 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111575589 | AATAACAATATAAAC[A/G]ACCACACATTTTAGA | 20840 |
rs46553459 | snp | C/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111571136 | TCGGTCTTGGAGATA[C/T]GATCATGTTTTGCCC | 20840 |
rs46555475 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111621871 | GTACGTCATACTTAG[C/T]TTAACCAAAGCTTGT | 20840 |
rs46559659 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111681363 | TCTTTCTAAAGTGTG[A/G]AGAGCCGAAAGTGTC | 20840 |
rs46568554 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111650701 | AACTCCAATCCCAAA[G/T]GTGTGCAGAGCCTTA | 20840 |
rs46574180 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111610334 | TCACCAATAGGAAGT[A/G]TAGACGTGAGTTTAA | 20840 |
rs46579949 | snp | A/C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111636337 | GTCCCTGCACTAAAA[A/C/T]CACAAAGGGTCCAGC | 20840 |
rs46581770 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111579945 | GAATATCTAACCACA[C/T]AGAATTCCAGGCAGA | 20840 |
rs46586485 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111632796 | TCCCCCCCCCCCCAC[A/C]CACACCTCAGGCATA | 20840 |
rs46595191 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111641542 | GTGAAGTTCTGAGTG[C/T]GTGATAACAAGGTTT | 20840 |
rs46598334 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111658690 | AGTGGCAACATGTGC[A/G]ACCCACTGAATCTGT | 20840 |
rs46600742 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111668902 | TCCACTCACGTGAAT[C/T]CCAGGTTTCCTGTAA | 20840 |
rs46605875 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111686875 | AAGATCTACAGGCAG[A/G]TGTAGTGATGTATGT | 20840 |
rs46610808 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111677317 | CTGACCTGTATTTCC[C/T]TATTTCTTCTCCCCA | 20840 |
rs46617830 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111630519 | ATGGCTGAAAGAGGC[A/G]AGAAGAAATCACACT | 20840 |
rs46620482 | snp | A/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111571123 | TAACACATCCAGATC[A/G]GTCTTGGAGATACGA | 20840 |
rs46621093 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111686740 | CCCATGTGGTGGTGG[A/G]GGGGGGCAGGACTGA | 20840 |
rs46622786 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111676223 | AGGTCAGCTATGAGC[C/T]TGATGCCTCCAGTAA | 20840 |
rs46624008 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111613530 | GATCCTAAAGTTACA[C/T]GAGGCCAACCAAGCC | 20840 |
rs46631918 | snp | G/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111569566 | CTTTCATCTTTTAGA[G/T]ACTTTTCTTAGAGAA | 20840 |
rs46633341 | snp | C/G | | | intron-variant | Stac | GRCm38.p3 | 9:111641358 | TTGAGAAGCTGCCAA[C/G]GAAGGGGACCTAGAG | 20840 |
rs46647104 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111641768 | TCTGGCTGTTGAGCT[C/T]TGCCCTTGAGAAGGG | 20840 |
rs46653172 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111666402 | GTGAGGTTTTGCTTT[C/T]CTGAAAATTCATTCA | 20840 |
rs46654153 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111606170 | AGATATTGTACTGAA[C/T]GTATCCTGAACTTTT | 20840 |
rs46655246 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111632031 | TGATTAGAAGTTAAA[A/G]ATTACCCTAATTAGT | 20840 |
rs46670963 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Stac | Mm_Celera | 9:111644315 | TTGAAGGAAGTCCCT[A/G]AAGCCTCGTGGCTTG | 20840 |
rs46682154 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111665470 | TGGAATCAGGCTGGT[A/G]ATTTTGAATGCTTGC | 20840 |
rs46686527 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111577535 | ATTTATATAAAACAT[G/T]TAGGCAAGTTCACAA | 20840 |
rs46690535 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111571359 | GTCCAGAAGGAAGTG[A/G]CTAAGCACATTATAG | 20840 |
rs46714795 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111687291 | GGCAAAAAAATAGGC[A/G]AGATAGAGAATAAAG | 20840 |
rs46715476 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111643378 | TTGTTGAAATAGTCG[G/T]TTTTTTTTTTTTTTT | 20840 |
rs46720838 | snp | C/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111578790 | TTTCCATCTTAAACC[C/T]GAGAGCCTTGAGGCT | 20840 |
rs46725823 | snp | G/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111653800 | AGGAACACGTAAAAT[G/T]CCAGATGTGAGCAGC | 20840 |
rs46744228 | snp | G/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571872 | AGTGAGTCACTAGGG[G/T]CGGGCTTTGAGGCTT | 20840 |
rs46771569 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111645934 | GTCATACACTGAGGG[C/T]TTAACACTCCACCCT | 20840 |
rs46773776 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111631580 | GCAAGAAGTCACAAC[C/T]GATTGAGGACAACTG | 20840 |
rs46792652 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111620217 | TTGAGAGTAAGGGAA[C/T]GACTTGTGTCCAGTT | 20840 |
rs46800779 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Stac | Mm_Celera | 9:111641835 | AGGATACAAGCAAGC[A/C]AGTAGGGTTGGTGCT | 20840 |
rs46805595 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111627844 | GGTACTGCATGTTAT[C/G]AAAGCTGATCTCGTC | 20840 |
rs46812696 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Stac | GRCm38.p3 | 9:111651693 | GCTACTAAACACATC[C/T]AGGAAGAATGGGAGA | 20840 |
rs46826955 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111626117 | TAGGCTGGCATGGAA[G/T]CTCAGAGAAAAAGTT | 20840 |
rs46833332 | snp | C/T | 0.152778 | 0.230321 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111572763 | AGTATTCAATAAGTA[C/T]CAGGGTATATTTTGC | 20840 |
rs46851407 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111570447 | TGGAGTCACATATAG[A/G]AAAGAAAACTGTTGA | 20840 |
rs46857848 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111658626 | TGGGACAGAGTGTCA[C/G]TGCAATAGGCACCAG | 20840 |
rs46857882 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111658566 | AAATGTAGGCTGCTG[A/T]GCTAATTCGAAGTAA | 20840 |
rs46864162 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111671167 | AAAACGGATGTTGCT[G/T]CCTTGTGGTTAATGC | 20840 |
rs46867298 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111638397 | CCGTGTCAGGCAAGG[A/G]GGTCTGCCTGCTTCT | 20840 |
rs46867987 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111610413 | GGAAGTGGTGGCACA[C/T]GCCTTTAATCTCAGC | 20840 |
rs46870440 | snp | C/T | 0.244898 | 0.249948 | missense, upstream-variant-2KB | Stac, Gm36034 | GRCm38.p3 | 9:111593749 | TCTTCATTTGATCTC[C/T]GAAGTCATCCATACC | 20840 |
rs46896375 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111629818 | ATGGGAGGATGCCTG[C/T]GCTATGCTGGCCAGC | 20840 |
rs46915604 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111652780 | ACAATGGTGTCATTG[C/T]TACTGCTGGCATTTG | 20840 |
rs46919037 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111563190 | ATATTCCAGAGCAGG[C/T]GCCTGTATGAGACTT | 20840 |
rs46924661 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111667129 | AATCTTTACTATATC[A/G]TTATCTGTACCATTT | 20840 |
rs46931918 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111645717 | GATGTTGACTGTGTG[C/T]CTCACAGAAAAAGCC | 20840 |
rs46938289 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111650750 | GGAACAGCCAATCCA[A/G]GGAGGAAGACAATCA | 20840 |
rs46945939 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111633912 | CAGGACAAAGGCTGT[A/G]CTGATGTACTTCATA | 20840 |
rs46979708 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Stac | GRCm38.p3 | 9:111636063 | CGCACAGATGTGAGC[A/G]CAGGAGCTTTGCGCT | 20840 |
rs47001741 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111562942 | ACCTGGGTTTGGAAA[A/C]AGTCCCAGATGCAGA | 20840 |
rs47009627 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111639444 | ATTAACAAGCAAAAA[C/T]GTGTGGACAAAAGGG | 20840 |
rs47026392 | snp | A/C | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111644889 | TTTTTTTCTGCAGTG[A/C]CTCCTGGGTATGATA | 20840 |
rs47028039 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111634155 | TCACAGATCAGATCA[C/T]ATCTGAGGTTGATAC | 20840 |
rs47038037 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111666420 | GAAAATTCATTCATA[G/T]ACACTGATTGCCCCT | 20840 |
rs47039658 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Stac | GRCm38.p3 | 9:111647270 | TGCCCTGTGGATTAG[A/C]AGGAAACAGAGAAAA | 20840 |
rs47046137 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111656577 | CTCTCATCTCAACTC[C/T]TGTCACATTATCAAT | 20840 |
rs47048615 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111674156 | GGAGATGCTCATCCC[C/T]GGAGCCGACTGCACA | 20840 |
rs47053792 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111634045 | CATTAATAACCCACC[A/T]GTGTTTGACCTACCA | 20840 |
rs47059733 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Stac | Mm_Celera | 9:111640653 | GCAACCAATGAGGAT[A/G]CAGCAAGGGTAGGAA | 20840 |
rs47060891 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111578700 | TAATCAGACTAATTT[C/T]TCAGTTTGCGTTAAT | 20840 |
rs47067889 | snp | A/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111573872 | TCAGAAGCACTCTTT[A/T]AAAAACCCTCATTTT | 20840 |
rs47069872 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111665665 | AGAACAAGGTCATTG[A/G]CTTTTACATTTCTGG | 20840 |
rs47078502 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111644619 | CTTTCCAACCCCCCC[A/C]AAATGAATTAAGCTT | 20840 |
rs47079333 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111645272 | GGGCTTAATCTATTT[A/C]CAGATGGAGTGTGTA | 20840 |
rs47083210 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Stac | Mm_Celera | 9:111669049 | CAGAAGAATACCTGT[C/T]TTTTTCTTCACAAGA | 20840 |
rs47085168 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111577134 | TTTGTCTTGTATTTG[G/T]AAGTCAGAAAAATGA | 20840 |
rs47093030 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111621914 | TACACTTTCTGGATG[A/G]TTATTTATGCATTGA | 20840 |
rs47094308 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111633602 | TTGTCTCGGTCAGTT[C/T]GTCTCGGTCTGGTCC | 20840 |
rs47094897 | snp | A/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111615910 | TCTTGCTAACCGTTC[A/T]TAAGAGTTGTGGCCA | 20840 |
rs47103283 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111570464 | AAGAAAACTGTTGAT[C/T]AAATTGAGTAAAACA | 20840 |
rs47106025 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111614514 | GGATTTTGTTTAACA[A/G]CGTATTATGGCTTCT | 20840 |
rs47109366 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111634647 | TTGCCTTTGCTTTGG[A/G]TAAGGCCCCTCCATC | 20840 |
rs47110952 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111681605 | CAACAGGAAACCACC[A/G]CTAGATTTTAATCTA | 20840 |
rs47116070 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111665559 | ACCCCAGTGACCTGA[C/T]CCTGGACTCCAGCTT | 20840 |
rs47144117 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111621648 | AAGCAGAGGCCAGGT[A/G]CAAAGGCTCTGCCAC | 20840 |
rs47146116 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111657519 | CTGAGAACAGAGGAG[A/G]TTTGAGCATTCACAT | 20840 |
rs47152724 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111569642 | TCTCTGTCCTGTCTA[C/G]AACATTATCACCTCA | 20840 |
rs47164569 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | Mm_Celera | 9:111581839 | AGTTGGGATACATAA[C/T]TACATTGTCTAAGCT | 20840 |
rs47168682 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111641033 | AGGCATGCCCTTTTA[C/T]TAGAAGAGCATCAGA | 20840 |
rs47172501 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111640803 | GCTCTAGGGAGTGTT[C/T]GAGAAACAGAAGGTT | 20840 |
rs47173352 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111674614 | GGGGCCACATGTGTA[C/T]GCTTCATTTTCAATT | 20840 |
rs47188287 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111629234 | AGACTTAAAATTTTA[C/T]GCAAGGAAATTCAAC | 20840 |
rs47196869 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111626162 | GAAGATAGGTTTTTA[A/T]TTAGTTCTCAATAGA | 20840 |
rs47199635 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111651691 | GTGCTACTAAACACA[C/T]CTAGGAAGAATGGGA | 20840 |
rs47201450 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Stac | GRCm38.p3 | 9:111569679 | AAACTCCTTCCCTCA[A/G]GAGAGCCTTACTGTT | 20840 |
rs47209935 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111577189 | AATAGCCAAAGAAGA[G/T]TCTAGGATGCTGAGC | 20840 |
rs47220082 | snp | A/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111571317 | GTCCTGTTTGTTTCT[A/G]TCTATATTCCAGGGG | 20840 |
rs47268793 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111673365 | TGAGGGTTTACAATA[C/T]GGATCTTGTGTTTAG | 20840 |
rs47274512 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111644834 | AGTAATAGCACCACA[C/T]CAGAAATCTCCAAAG | 20840 |
rs47277498 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111584466 | TGAGTGACTTACCTA[A/G]GACTTGAGCCATGGC | 20840 |
rs47295823 | snp | G/T | 0.391111 | 0.206368 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577717 | AAGTGTGGAGTTAGA[G/T]CCAGGTGAAAACCCC | 20840 |
rs47301770 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111646678 | AAGGGACAGCACTGT[A/G]TTCCTAGAGTGATGC | 20840 |
rs47311715 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Stac | GRCm38.p3 | 9:111629008 | TTGCTTCTAAAGGGT[C/T]TCTTTACTTGGTCCA | 20840 |
rs47316324 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Stac | GRCm38.p3 | 9:111636241 | AAGTCCACGTCTTGA[A/C]AATTAAATAGTGAGA | 20840 |
rs47321613 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111614684 | AGACCTTTCACAAAA[C/T]GCTCAGTTCTGAGTT | 20840 |
rs47327369 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111621140 | ATCTTGAGTATGGGA[A/G]CTGTCATGCTGTTGA | 20840 |
rs47343815 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111674757 | GCTCATAGATGAACA[A/G]TTTCTATGGATGAGC | 20840 |
rs47345594 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stac | GRCm38.p3 | 9:111685744 | GTTGTGTATATGTTA[C/T]ATGCTCAGACACTGC | 20840 |
rs47353399 | snp | G/T | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111608710 | CATGCTATTTTGTCA[G/T]AGCCTGGTCTTGGAG | 20840 |
rs47362883 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577356 | TCTCCATTTTCCTTC[C/T]AGACAAATACATTAT | 20840 |
rs47375695 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111619800 | CAAATAGTAAGATGG[C/T]CAGACCTTTCCCTCC | 20840 |
rs47377107 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111639962 | TGGAAGAGCAGCAAG[G/T]GCTCGTAACCACCCA | 20840 |
rs47381731 | snp | C/T | 0.18 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111581654 | ACCAGTTCTCCCATT[C/T]GTTAATGGGTCAGAG | 20840 |
rs47384878 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111656138 | GACAAAGTCCTCTCT[A/G]AGAAACTGGTGATGC | 20840 |
rs47388263 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111578974 | ACATTAGTGACATTC[A/G]GGAAGGTCTGGGCTT | 20840 |
rs47389980 | snp | A/C | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111572117 | GGTTCCTGGCATGTC[A/C]GTTTTGCATGTAGGA | 20840 |
rs47413451 | snp | A/G | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111615971 | AAGTTTGGCCTTCTG[A/G]AGAGTCTTCCAAGTA | 20840 |
rs47426318 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577328 | GAGGCTAACACAGCA[C/G]CCTCTGATGGCATCT | 20840 |
rs47435006 | snp | A/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111571322 | GTTTGTTTCTGTCTA[A/T]ATTCCAGGGGCTGGG | 20840 |
rs47442352 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111675871 | AGGAGACAAAGGGCC[C/G]AAGCAATCCCTTGAT | 20840 |
rs47452838 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111683910 | ATGCATACGTGTGTC[A/G]ATTGTACATGAGCGC | 20840 |
rs47453658 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111644686 | TGGTCTTAAACTTAC[G/T]ATGAAGCGAGGATAA | 20840 |
rs47465422 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | Mm_Celera | 9:111569902 | TGAAAATTCGGGAGC[C/T]GATGCATACTAGCAT | 20840 |
rs47468268 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Stac | Mm_Celera | 9:111627859 | CAAAGCTGATCTCGT[C/G]TTTGAGGAATTTAGC | 20840 |
rs47476445 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111643379 | TGTTGAAATAGTCGT[C/T]TTTTTTTTTTTTTTT | 20840 |
rs47477537 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111607342 | CATGCTCAGGAGGTA[C/T]TAGCCACAGGGCTTT | 20840 |
rs47481500 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111606124 | TCCCTACCCTGAAGG[C/T]CTGTCTTTGGTGACA | 20840 |
rs47483650 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111608008 | CACAGCATTTGATGA[A/G]GCCACGGTAGCCGAT | 20840 |
rs47486480 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Stac | GRCm38.p3 | 9:111658131 | CTGACAGTACACTGA[A/G]CAGTTCTGAGGAGTG | 20840 |
rs47491978 | snp | A/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111570626 | GGAGAGGATGGCTAG[A/G]GAGATGACAACAGCA | 20840 |
rs47498829 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111577262 | CACTAGAAGCACAGA[C/T]ATGGCAAGATTTCTC | 20840 |
rs47530060 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111570296 | GGTTGCTATGCAGTT[C/T]AGCCTAGCTTTTAAC | 20840 |
rs47533366 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111607327 | AAGCCTGATATCCTT[C/T]ATGCTCAGGAGGTAT | 20840 |
rs47537358 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Stac | GRCm38.p3 | 9:111677120 | TCCTTGTGGATATTA[G/T]AGTTTGCAACACTAA | 20840 |
rs47547875 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111684130 | GTAATAACAGACAAA[A/G]CAACTACAAAATAAA | 20840 |
rs47552309 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111620622 | AAAGAACTCAGTCTA[C/T]GAAGTGCAAGCAAAG | 20840 |
rs47572069 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111628751 | CCCAGCTGAGGATGT[A/T]GCCCTTTCATTGAGG | 20840 |
rs47573221 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111674120 | AAATGGAGGAAGCTC[A/G]GAAGCTGCTGAGGGT | 20840 |
rs47575018 | snp | G/T | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571139 | GTCTTGGAGATACGA[G/T]CATGTTTTGCCCAGC | 20840 |
rs47576757 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111683835 | TTCAGTGATGTTGAC[C/T]ACTGGGCTTGGCTAG | 20840 |
rs47578195 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Stac | GRCm38.p3 | 9:111584031 | GTTCTCTGAAATAAA[A/G/T]AGTCCAAATAGAGTC | 20840 |
rs47583266 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111684753 | ACCCTTATAAGCTTT[C/T]ATGTTGTCACCAAGT | 20840 |
rs47595013 | snp | G/T | | | intron-variant | Stac | GRCm38.p3 | 9:111685690 | GAGAAAAATGGATAT[G/T]TAGAGATTTTTGTAT | 20840 |
rs47596726 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Stac | Mm_Celera | 9:111570192 | TTGTGTGGGGCTTCT[G/T]TCTTTTAAACACTGG | 20840 |
rs47605072 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111571060 | ATCTGTGAGACTTCA[C/T]TGTGAAAGAAAGGAA | 20840 |
rs47609467 | snp | A/C | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111655024 | CATCAAGGCTTGTAT[A/C]TGGAGTTTATTTACT | 20840 |
rs47615152 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111563543 | GTATACAATTTCTTC[C/T]TGACCAGGCCAGCAC | 20840 |
rs47655353 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111636351 | ATCACAAAGGGTCCA[A/G]CTCCTGCTGCTCAGA | 20840 |
rs47657313 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111564454 | CCTCTAATGCGGCCC[A/G]GGCCCAGGCAACAAG | 20840 |
rs47661623 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111672443 | CACAGGCATGTGTAC[C/T]GACCTGCATATGTAT | 20840 |
rs47664790 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | GRCm38.p3 | 9:111666519 | TTTCTCTGCATGGGT[A/G]TTTGTGTTTGTGGAC | 20840 |
rs47667006 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111605980 | AAGCTAGACTTGCTA[A/T]GCTCCAGGGCTGGAA | 20840 |
rs47671672 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111639479 | TTACGGGACACACTG[C/T]GACACACTACAGTTT | 20840 |
rs47683562 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111625266 | AGGAAAACAAAAGGA[C/T]GTGGGCATGAAAAAA | 20840 |
rs47684359 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111627396 | GGGGGTTAATGCTTT[A/T]GGTACCTTCACTCTT | 20840 |
rs47700315 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111631356 | TTGTTTTTAAAGATA[A/G]AAGAGCAGTCGGGAT | 20840 |
rs47703379 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111688221 | ATCCAGCTCTAAATA[C/G]GACTTCAAGAAAAAC | 20840 |
rs47708000 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111647506 | GTCAGCTGTGATAAA[C/T]AGAGTGCTCCTCTGA | 20840 |
rs47714788 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111654891 | GCAAGTGCTTGACCC[C/T]GAGAGAGCTGCAGTA | 20840 |
rs47718101 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111578710 | AATTTCTCAGTTTGC[A/G]TTAATCTGGTCCAGA | 20840 |
rs47724966 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111616113 | TGGCAGGACAGAAAA[C/T]GGGCAACTCCATGTG | 20840 |
rs47727297 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111641843 | AGCAAGCCAGTAGGG[C/T]TGGTGCTTATTGGAT | 20840 |
rs47744621 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111673521 | AGAGTCAGCTGGAAA[C/T]TGGCTTTTCTGAATG | 20840 |
rs47746748 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111578481 | CTTATCAAAATGCAG[A/G]AGAGTTGCCCATATC | 20840 |
rs47786251 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Stac | GRCm38.p3 | 9:111634176 | AGGTTGATACCTGAA[A/C]CTCCCTGCTTTTCTG | 20840 |
rs47787184 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111651581 | TCAATATGGGTGTGG[C/T]GGAGAGACTCTACAA | 20840 |
rs47789830 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111656487 | CAGTCACTGAGGATG[A/C]TAAGACATCACCATC | 20840 |
rs47817565 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stac | GRCm38.p3 | 9:111666408 | TTTTGCTTTCCTGAA[A/G]ATTCATTCATAGACA | 20840 |
rs47827690 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111651914 | AGTGTGACAAGGACT[C/T]GCTATGTAATAAGGT | 20840 |
rs47829889 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111647202 | CCTGTGGTGTGTTGC[A/C]TGCCCTGCCCTGCCT | 20840 |
rs47844870 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111671651 | ATTAAAAAAACTCAT[A/C]GGTTGGCACGTAACA | 20840 |
rs47849749 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111580104 | TTGTCTTGGGCAACC[A/G/T]CACAGCTTTTCTGGA | 20840 |
rs47875144 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Stac | GRCm38.p3 | 9:111636495 | CACCCGCCTTTCTGC[A/C]ACCCAGATAGAAGGA | 20840 |
rs47876452 | snp | C/G | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111637951 | CAAAAGGGGACTCTA[C/G]TGGAGACCACAACTT | 20840 |
rs47882249 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111673674 | GGTCTAATTAGTTCT[A/G]TGTTCAGATGGGATG | 20840 |
rs47887006 | snp | G/T | | | intron-variant | Stac | GRCm38.p3 | 9:111629404 | GGACCTGTAGGGGAA[G/T]TTTTCCTTAATTGAT | 20840 |
rs47888109 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641057 | CATCAGAGAAGACAT[A/G]TTGTCATGGAGACCA | 20840 |
rs47906734 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111654699 | ATTCAAAACTGGCAG[A/C]GTGTATTCTCTCCTG | 20840 |
rs47910206 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111673571 | AGGATCTCAGGGGCT[A/G]AGAATGTATGCAAAA | 20840 |
rs47961900 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Stac | GRCm38.p3 | 9:111688286 | TACCAGAGGGTCCAG[A/G]AGGCCCTTGGTAGAA | 20840 |
rs47964030 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111630485 | AGCTTGAATAGGTGA[C/G]CAATTCTTGCAGGAG | 20840 |
rs47972324 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111625551 | AGGGCTCTCAGGAAC[C/T]TCTGTACAATGTGCA | 20840 |
rs47974790 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577187 | TGAATAGCCAAAGAA[A/G]ATTCTAGGATGCTGA | 20840 |
rs47992328 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111615889 | CTGACTACTTGTGGC[A/G]AATCATCTTGCTAAC | 20840 |
rs47993138 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Stac | Mm_Celera | 9:111640122 | GCTGGGTCTTGTTCA[C/T]AGCAGTCTACCACCG | 20840 |
rs47997814 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111634690 | CACATTGACCTTCTT[A/G]CATTTAACTCTCTGA | 20840 |
rs48010007 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111650504 | AACTTAGGTCTTGAG[A/G]AAAGAAGCCAGTTTA | 20840 |
rs48016942 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111664813 | CCACCACAGGAGGTA[A/G]CCAAGGTGGTCTGGG | 20840 |
rs48025698 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111669474 | ATGCTGTGGTTGGAC[C/T]ATAAGGTATCACTGA | 20840 |
rs48027742 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111658443 | AGTGCAGCAACATCG[C/T]AAGTGGCAAAAGCCT | 20840 |
rs48065527 | snp | A/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111633919 | AAGGCTGTGCTGATG[A/T]ACTTCATAACACCCT | 20840 |
rs48083212 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111654232 | GAATGATGGCCCTAG[C/T]ATTTTTATGCAGTGA | 20840 |
rs48098738 | snp | G/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111632379 | AATTGAAAACCCATA[G/T]CCTATGCTACATTTG | 20840 |
rs48104937 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111652454 | TTGTACCTGGAACAT[A/G/T]GTCAATAAAGGAGAA | 20840 |
rs48116355 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Stac | Mm_Celera | 9:111634767 | TCATTCCTTTTCCCA[A/G]GGACATTGTACCTGT | 20840 |
rs48121461 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641402 | GGAAGCTAAAGGCAC[A/G]GAATGATTGGGAGAA | 20840 |
rs48124049 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111671817 | TCCCAGCAGGCTGTG[C/T]ACGCTTACAAGGAAG | 20840 |
rs48155299 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111652382 | TGACAAAGGACCGCC[A/G]ATAAGCAGAAAAAGC | 20840 |
rs48161281 | snp | C/G | | | intron-variant | Stac | GRCm38.p3 | 9:111562872 | GGAAGTGGGGGGCGG[C/G]GGCGGGGGCGGCCGC | 20840 |
rs48169846 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111614634 | AGAGTTGGCCTTACA[C/T]TATTACAAGGTTCCC | 20840 |
rs48173409 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Stac | Mm_Celera | 9:111644494 | AACACTTGGAGGTGA[C/T]AGAAGACCACACCTT | 20840 |
rs48173601 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Stac | Mm_Celera | 9:111569462 | CTGCAATAATGTGAT[A/C]TTTTTGGTACCTGTC | 20840 |
rs48190724 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111570515 | AGTTATAATTATAAA[A/G]TAATGACTGATTGTG | 20840 |
rs48193164 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111636358 | AGGGTCCAGCTCCTG[C/T]TGCTCAGACTCCTGG | 20840 |
rs48198935 | snp | C/T | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111640538 | AGTGGCAATAACTAG[C/T]CTCAAGACATTGCTG | 20840 |
rs48200267 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111583020 | TCCAGCACCTCACAC[C/T]AGACTGTAAATTATG | 20840 |
rs48206862 | snp | A/G | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111572677 | AGAAGTAAAGGAAGC[A/G]TGTTTCCACTGGCTC | 20840 |
rs48208345 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111574812 | TAAGAATGTAGGGCA[A/G]AAGTCACACTCTCTA | 20840 |
rs48211561 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111650982 | ATACCAGAAGATAAA[C/T]AGGAACAAAATGCAT | 20840 |
rs48221689 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111644439 | AAGTCCATTCTTCAG[C/T]GTGTAGGGTGTATTT | 20840 |
rs48228221 | snp | G/T | 0.244898 | 0.249948 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111573998 | GGTCACTGCCAAGTC[G/T]CAGTTATTTTGGTCC | 20840 |
rs48235677 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111579254 | AGAGGGTTGTATACA[A/G]TGGGCAAGGTGAACT | 20840 |
rs48237217 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111646256 | ATTGGTGAGTCCTAG[A/G]TTTAATGAGAGACCC | 20840 |
rs48238703 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111637566 | GTAAATTAACCCAGT[C/T]TCAGAAAGAGAAATA | 20840 |
rs48248345 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111630200 | AATGCTGTAGTAGTT[A/G]GCATATAGTAGTTAG | 20840 |
rs48256983 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111660641 | AAACTGATAGTGAAT[A/G]GAGGCAGATGGATAG | 20840 |
rs48258870 | snp | A/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111659028 | CCCCAGTTAATCTGT[A/T]CCGTGCTTCTCATCT | 20840 |
rs48259532 | snp | A/C | 0.46281 | 0.131194 | intron-variant | Stac | Mm_Celera | 9:111645172 | AGATGCCAGTTGCTC[A/C]TGCGTAAGTAAATAG | 20840 |
rs48271277 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111637067 | CTCTTCCCTCAGCCC[A/G]CTGCTGAGAGTTCAG | 20840 |
rs48297858 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111631273 | CATGTTCTCCTCAAA[A/G]AAGACACAGTTTGCT | 20840 |
rs48301704 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111629257 | AATTCAACATTTTTT[C/T]CCAACAATCTGTTAA | 20840 |
rs48317873 | snp | C/G | | | intron-variant | Stac | Mm_Celera | 9:111583577 | CAAAACCTGCCATCT[C/G]TTCTCCCTATCCCCC | 20840 |
rs48332844 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111645842 | ACATGTACACCATGT[A/T]CAAAGCTAAGCTTTG | 20840 |
rs48335116 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Stac | GRCm38.p3 | 9:111646989 | TTTATCCTTACCTAT[A/C]GAAGAGTTTTTGCCA | 20840 |
rs48337866 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111671931 | TGCAACTGACAGCAT[C/T]GGCGTTTGATTAGCA | 20840 |
rs48355530 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Stac | GRCm38.p3 | 9:111654723 | TCTCCTGACCAATTC[C/T]CAGTTCAATTGAAAG | 20840 |
rs48376514 | snp | A/C | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111609756 | TCACCCCACTAAACA[A/C]TGTAGCTTAGAACAA | 20840 |
rs48383316 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111650114 | ACAGGAAGTCAGATT[G/T]GCATTTTGTTTCAGA | 20840 |
rs48391065 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111639539 | GTGGGGGAGGTTGCA[A/G]GGGTGGAGGGTAGGT | 20840 |
rs48403947 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Stac | GRCm38.p3 | 9:111638121 | TGTTATTGGAGCCTC[C/T]GAGAAATGAAGGAGA | 20840 |
rs48414699 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Stac | Mm_Celera | 9:111632830 | ATACACTTTTAAAAA[G/T]GCAGCCACAATATCA | 20840 |
rs48433755 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111652011 | ATCACTAAAGACTAT[A/G]TTATTGGAGGAGGTA | 20840 |
rs48440779 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111628420 | TTCTCACCCAACTAA[C/G]TCTTTGCATATGCAC | 20840 |
rs48442167 | snp | A/G | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111578791 | TTCCATCTTAAACCC[A/G]AGAGCCTTGAGGCTG | 20840 |
rs48452149 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111669291 | AGCTATAGCTCCAAC[C/T]TGATCTAATTGCTGT | 20840 |
rs48452272 | snp | C/T | 0.277778 | 0.248452 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577820 | TAGATTATGGAATAT[C/T]GTTATTTTGAAAAGT | 20840 |
rs48458957 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111582902 | TCTCACAGGCAGACT[C/T]CTGCAAGTCGGATGC | 20840 |
rs48461219 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111659174 | ACTCCACTTTCAGCT[C/T]TCCTGTTACTGTTCA | 20840 |
rs48464052 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111655719 | AAGATGTTAAATTAC[C/T]AGTGTGACCTGTCTA | 20840 |
rs48473114 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111629495 | ATTGTCAAGAGTGTT[C/T]GGTTTCAATGTAAAA | 20840 |
rs48489547 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111572152 | AACTACCCTTGTACC[C/T]TGGGCTTATAATCAT | 20840 |
rs48497590 | snp | A/C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111638519 | CCTCATGCCCCCCTC[A/C/T]CCCCTCACCACCTGC | 20840 |
rs48502082 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111650950 | TGAGTGGAGAGGTGG[A/G]ACAGATTTTAACGAA | 20840 |
rs48503522 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111582196 | GTGAGGAACTTAGCT[C/T]GTTCCCAGAGATCAC | 20840 |
rs48509706 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Stac, Gm36034 | GRCm38.p3 | 9:111593917 | CTTCCTACCTTCATT[C/T]TTTCAGGTCCCTCAT | 20840 |
rs48529187 | snp | A/C/T | | | intron-variant | Stac | Mm_Celera | 9:111632794 | CATCCCCCCCCCCCC[A/C/T]CACACACCTCAGGCA | 20840 |
rs48531512 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Stac | Mm_Celera | 9:111687231 | TAGAGGCAACATTTA[C/G]TAGATACTCAGGACT | 20840 |
rs48531966 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641918 | TGTGTGCAGGTACAT[A/G]TGAAGGCCAGAGAAC | 20840 |
rs48535118 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111629607 | AATCTGAAGTTTAAA[C/T]TTTGAGTCCACAAAT | 20840 |
rs48551456 | snp | C/G | | | intron-variant | Stac | GRCm38.p3 | 9:111569441 | CTGAGGGCAAGGCGG[C/G]GTGGCCTGCAATAAT | 20840 |
rs48552400 | snp | A/T | | | intron-variant | Stac | Mm_Celera | 9:111645361 | GTCTTTGAGGTATAC[A/T]CATGAGGGTTCATTA | 20840 |
rs48558630 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Stac | GRCm38.p3 | 9:111658587 | TTCGAAGTAATAATC[C/T]CATAAAGCCCTTAGC | 20840 |
rs48558759 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111643272 | AAATATCTCATTCTG[A/G]ATTTTCCTACGTGAT | 20840 |
rs48560005 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111636031 | CTAATCTGACCATGC[A/G]GGAGGAAACTTCTGG | 20840 |
rs48564552 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111640764 | GCCAGGAGGTGATGA[G/T]GGCAGACATTTATTG | 20840 |
rs48567245 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111656301 | TTTCAGAATGCCACC[G/T]GCTCTGCTAAGCTCT | 20840 |
rs48572438 | snp | C/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111650555 | TCAAGCAATGAGTGC[C/G]AGCCTTGCTGTCCCA | 20840 |
rs48594721 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111687489 | CAAGTGTGAGGATTA[G/T]AGCTCCATGGCCACC | 20840 |
rs48625168 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stac | GRCm38.p3 | 9:111649196 | TTATGATAATGATGG[C/T]CATTGCTATTGTTTT | 20840 |
rs48644759 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111584361 | TCTTTGAAGCCAGCC[C/T]GGGGACTAGGAGGAA | 20840 |
rs48647022 | snp | A/C | | | intron-variant | Stac | GRCm38.p3 | 9:111628996 | AAAGGAAATCTCTTG[A/C]TTCTAAAGGGTCTCT | 20840 |
rs48654289 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111664552 | GGTGTGTCATCCCTG[A/G]TGTGAGGACAACTGA | 20840 |
rs48656466 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111634192 | CTCCCTGCTTTTCTG[G/T]GACATGCTGACCACA | 20840 |
rs48681907 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111578532 | AGTTTTAATATTCCA[C/T]ACCCTAGCCTATTCA | 20840 |
rs48690148 | snp | C/G | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111639646 | TTTTTCTCCGTACAA[C/G]CTTAAAGGAGCCACG | 20840 |
rs48730289 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111664510 | CTTCCCATTGGACCC[C/G]CAGATTTGTTGCTGA | 20840 |
rs48734323 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111658429 | TGAAGACATCACGGA[A/G]TGCAGCAACATCGCA | 20840 |
rs48734628 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111644867 | GTGTTAGCTCTCCAC[A/G]TCTTTGTTTTTTTCT | 20840 |
rs48750085 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111576894 | GAGCTAGGGATGGTA[C/T]AACCTGACTATGTGG | 20840 |
rs48750705 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111629288 | TTAAATCTGAATCCT[C/T]TTAATATGCTATATC | 20840 |
rs48754185 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111624443 | TAATGCACTTACTTT[A/T]AATCAAAATGCTAAA | 20840 |
rs48788706 | snp | A/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111668815 | AATGAGTGCCCATAG[A/T]CTGTCTTATTCTCTT | 20840 |
rs48790734 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111650314 | CCTGCCACAGGGCTC[A/G]GGCCATCATACATGC | 20840 |
rs48817606 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | GRCm38.p3 | 9:111666582 | TCATACTTAAACTTG[A/G]TCCTGTGAGCCGCCT | 20840 |
rs48827292 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111673010 | ACTCAGCAATGAAAA[A/G]AAAGTACAAGTGAAG | 20840 |
rs48835458 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Stac | GRCm38.p3 | 9:111582797 | AAGATTTTCTCTGGG[A/G]TTGGCATTTGCCCCC | 20840 |
rs48837925 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111645201 | AGAGCCATGAGGGAG[C/T]TGGGCTGGGAAGGGT | 20840 |
rs48853439 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111563372 | TGGATGAAGGGATGG[C/T]GGAAGCTAAAGGGTT | 20840 |
rs48857935 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111687471 | TCTCCTGCCTCTTCG[C/T]CTCAAGTGTGAGGAT | 20840 |
rs48862626 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Stac | GRCm38.p3 | 9:111560960 | CTCCCAAAGGTCTTG[C/T]GCCTGGGACCCTGGT | 20840 |
rs48873315 | snp | A/C | | | intron-variant | Stac | GRCm38.p3 | 9:111638437 | GATTTTGTTGGAAGG[A/C]AATGGGACATTTCTT | 20840 |
rs48876050 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111687824 | GAATTAAAAAAAAAA[C/T]GAGTGTGTTTAGCTG | 20840 |
rs48878554 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111608813 | GGAGCTGTTCCACTG[A/T]GAGCGGTCCTCTGAA | 20840 |
rs48880541 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stac | GRCm38.p3 | 9:111666546 | GGACTAGCCATTTGC[C/T]GTCATACACTAGCTA | 20840 |
rs48881670 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111642146 | AGCCTCCTCTAGACC[A/G]GGATACAGATCTTTT | 20840 |
rs48883874 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111655401 | GCCTGAGCTGATATG[A/G]GCTATAGAGTCCCAG | 20840 |
rs48891502 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111645570 | ACTGTGGCCACTAAG[C/T]CCCACTATATTTGGT | 20840 |
rs48893555 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111623384 | TGAGTGTTTGCTCAT[C/G]TCTCCTTCCAGTCAC | 20840 |
rs48898448 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111640945 | GGGAAAGTGAACCCA[A/G]GAGTTTGTTGAAGGC | 20840 |
rs48901301 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111634722 | GCTCAGAGCTGGTCT[A/G]TGGGTCCCCTGAACC | 20840 |
rs48914736 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111591644 | CACAAGAGACAGCTA[C/T]ATCTGGGTCCTTTCA | 20840 |
rs48915838 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | Mm_Celera | 9:111631398 | TAGACCAGTGGTCTT[C/T]AACCTCCCAATACTG | 20840 |
rs48917333 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111639390 | TGAGTGGCAGAAGCC[A/T]GAGGCTTCCAACCAG | 20840 |
rs48921341 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Stac | Mm_Celera | 9:111644171 | CAATTCATTCTGGGT[A/T]AGATTCACAAGAGTT | 20840 |
rs48922629 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111640845 | TTGAGGTAAGGAGAC[A/C]TGCTGGGAGATGCCT | 20840 |
rs48924048 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111580025 | ATAACATTCTCCACA[A/G]GAATTTTATGGTTTA | 20840 |
rs48942770 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111672433 | TCCAGGCATTCACAG[A/G]CATGTGTACCGACCT | 20840 |
rs48943366 | snp | C/T | | | upstream-variant-2KB | Stac | GRCm38.p3 | 9:111692486 | GGGTTTACTTTTGTT[C/T]TGGGATTAATCTTCT | 20840 |
rs48958356 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111660131 | ATTTCACTTGGCTCA[A/G]TAACAGCTATTGTTC | 20840 |
rs48969022 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111633849 | CAGCAATAGATCTGA[C/T]GCTGCTTCCTTCCCA | 20840 |
rs48980076 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111640718 | GTTGTGGTAAGGGCT[A/G]TGGAATTTATCCTAA | 20840 |
rs48990824 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111646608 | TGCTATCCAGTCTGT[A/G]GAATTTTTATTACAG | 20840 |
rs48997235 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111642669 | AGCAATGGAAACTCT[A/C]ACTAAGACACATGGC | 20840 |
rs49000278 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Stac | GRCm38.p3 | 9:111687469 | GCTCTCCTGCCTCTT[C/T]GTCTCAAGTGTGAGG | 20840 |
rs49019133 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111676208 | AGTGGCTCTGTTAGT[A/G]GGTCAGCTATGAGCC | 20840 |
rs49038181 | snp | C/G | 0.391111 | 0.206368 | utr-variant-3-prime | Stac | GRCm38.p3 | 9:111562504 | GCCTGCTTCCAGATT[C/G]CTAGCACAGTCTCAG | 20840 |
rs49044785 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111566559 | AATAAACCCTTTCCT[C/T]CACAACTTGTTTCTT | 20840 |
rs49044876 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111628496 | TCTTTTCTACTAAAG[A/G]TTTGGTTAATAGCTA | 20840 |
rs49052877 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111639272 | GGGCTTTGAATTGAC[C/T]TATCCCAATATCTAC | 20840 |
rs49054766 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111629059 | GAGACCACAATCTCA[C/T]TCAATGCCTTCTCTT | 20840 |
rs49055421 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111686614 | TGGGATCAAAGACAT[A/G]CACCACCACTGCCTG | 20840 |
rs49060043 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111647010 | GTTTTTGCCAGGGGA[C/T]TGGTACTTTGTTTAA | 20840 |
rs49065739 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Stac | Mm_Celera | 9:111629131 | ACAACTGAGCACCCT[C/T]GTGATAATCCCTCCA | 20840 |
rs49067417 | snp | C/T | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111636075 | AGCGCAGGAGCTTTG[C/T]GCTTAAAATCCTCTG | 20840 |
rs49073912 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111673980 | ACAAGAAGGGACAAT[A/T]ACACGGAAGCAGAAG | 20840 |
rs49089684 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111651677 | CAAGGAGCAGAGTTG[C/T]GCTACTAAACACATC | 20840 |
rs49098906 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111636620 | AGGCTATGCATGAAG[C/G]TACCCTGTGCTGACT | 20840 |
rs49100687 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111641533 | ACAGAATTTGTGAAG[C/T]TCTGAGTGCGTGATA | 20840 |
rs49102491 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111646787 | CAGCCTACTAGGTAA[A/C]AAGAATGGAAAACAC | 20840 |
rs49119879 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111613441 | CCAAACTACACATAC[A/G]GAATACAGGATGCAT | 20840 |
rs49135546 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111578864 | GCTAAAGAGCCATTT[A/G]GAAGGAACTGGGGAG | 20840 |
rs49149681 | snp | G/T | | | intron-variant | Stac | GRCm38.p3 | 9:111637999 | CAGATTATGCACCCT[G/T]CTCCCCACCAGAAAT | 20840 |
rs49155835 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111627828 | CGGACACTCAGAACT[A/G]GGTACTGCATGTTAT | 20840 |
rs49157520 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Stac | Mm_Celera | 9:111638267 | GGAAGTTACACCAGG[C/T]CTCAGGAACATGGAA | 20840 |
rs49161414 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571416 | GAGCAGAAGGTATCA[A/G]GAATGTGTCGATTAG | 20840 |
rs49173077 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111674969 | CAGGGATGGGTAAGA[A/G]CTATCTCAGTAAATC | 20840 |
rs49182548 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Stac | Mm_Celera | 9:111623904 | AGTGCCAGGAAAAAA[A/G]ACAGACAGAGAAAGA | 20840 |
rs49183399 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Stac | Mm_Celera | 9:111675224 | ACTGCTTCCAGTCTA[C/G]ACCCAGACCTGATGG | 20840 |
rs49206909 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111642327 | CCAGATCACTACCTA[C/T]TTTACAGATGAGAAA | 20840 |
rs49210075 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Stac | GRCm38.p3 | 9:111666614 | GTGAGTTTTCTGTGC[A/G]GATAACGTTCTGACT | 20840 |
rs49213761 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111653591 | AAGCCTGTTGGCTGG[C/T]TCATGTTAGGTCCTC | 20840 |
rs49216380 | snp | A/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111570624 | TGGGAGAGGATGGCT[A/G]GAGAGATGACAACAG | 20840 |
rs49238139 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111644501 | GGAGGTGACAGAAGA[C/T]CACACCTTGATGTCA | 20840 |
rs49245978 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111638179 | AAAAGCAGGTTCAAC[A/G]TTAGCCTGCCTTCTG | 20840 |
rs49250359 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Stac | Mm_Celera | 9:111680889 | CTAATTTGCTCCTTG[C/T]TTTCAAAAGTGAGTC | 20840 |
rs49262781 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111655429 | CAGATGTGGGATAGT[C/T]AGTGGAAAATATCTA | 20840 |
rs49279562 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111673764 | AGGCTGCCACGAGAG[A/G]GGAGAAGACCAGACT | 20840 |
rs49292852 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111627659 | CTCATTTAATGTTCT[C/T]TGCCCAGAAGTATGT | 20840 |
rs49293467 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | Mm_Celera | 9:111585426 | GTAAGGCTTTCCTTG[C/T]TCCAAGGCAGATCCG | 20840 |
rs49298544 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111629236 | ACTTAAAATTTTACG[C/T]AAGGAAATTCAACAT | 20840 |
rs49300167 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111654039 | ATGAAGCCAAGGATG[A/G]CATACTTACTGGTGA | 20840 |
rs49308564 | snp | C/T | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111571104 | GGCTCCCAGCATCCT[C/T]CTCTAACACATCCAG | 20840 |
rs49311871 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111656106 | AACTTACAGACGGTG[C/T]CATTGACAGTCAGAA | 20840 |
rs49319722 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Stac, Gm36034 | Mm_Celera | 9:111594039 | TTGGAACTCAAGTCT[C/T]TTCTAGCAGTGTTCC | 20840 |
rs49328209 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111574759 | TGGATACTTCAGGAT[G/T]TAGAATCTCATGTGA | 20840 |
rs49330831 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111642220 | GTGTCAAGAACTGGA[C/T]GAGAGACTAACTTAC | 20840 |
rs49364181 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | Mm_Celera | 9:111680922 | TCTGTCACAAGAAAA[C/T]TGGATCTAGAGTGCT | 20840 |
rs49366987 | snp | A/T | | | intron-variant | Stac | Mm_Celera | 9:111570308 | GTTCAGCCTAGCTTT[A/T]AACTCACTACATACA | 20840 |
rs49371955 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | GRCm38.p3 | 9:111667276 | ACAGGAACACAGACA[C/T]AGAAAGATTAAGCAA | 20840 |
rs49373603 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111619385 | TTCCTATTTCGGTTC[C/T]TGACGACTAGTGGAA | 20840 |
rs49383056 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Stac | GRCm38.p3 | 9:111679407 | GGATAGAGAATTTTA[A/C]AAATAAACAGGAGAT | 20840 |
rs49388184 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111669576 | TGGTCCTTTACTTCC[A/T]CAGAGGCAGGATGGG | 20840 |
rs49401310 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Stac | Mm_Celera | 9:111646946 | CACTCTCACCTTATA[C/T]TAAGTGGTCAGGACT | 20840 |
rs49408849 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111640315 | TGATCTCCCTAAGGT[C/T]TGACGTCTAATAGTC | 20840 |
rs49410841 | snp | C/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111572029 | CATGGTCTGAAACTC[C/T]AAGCTAAAATAAACA | 20840 |
rs49423573 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Stac | GRCm38.p3 | 9:111638479 | CTGCTTGAAAGACAC[A/G]CCTACCTGGATGAGG | 20840 |
rs49440509 | snp | A/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111616229 | CCCTTGTCAGGCTGG[A/T]GATATGAAAGTGGGG | 20840 |
rs49452909 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111687724 | AATTAATCCATATAA[C/T]GAGAAAAAAAAAACC | 20840 |
rs49454307 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111578203 | GTTTGTGTAGACCCA[A/G]TCTCCTTTCCCTTTA | 20840 |
rs49457517 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111610424 | CACATGCCTTTAATC[C/T]CAGCACTTGGAAGGC | 20840 |
rs49460061 | snp | A/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571492 | CTGTATTTTGTCTCT[A/G]TCTTATGTTATTATG | 20840 |
rs49462159 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111652396 | CGATAAGCAGAAAAA[G/T]CCAGAGCATTAGGAA | 20840 |
rs49467018 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111658350 | ACATCAGGTCATTCA[A/G]GAAGTGTAGTCATCA | 20840 |
rs49474439 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577570 | TGATGGCCACCATTG[C/T]TCTGAAGCCATTATT | 20840 |
rs49482182 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111638282 | TCTCAGGAACATGGA[A/G]CCTCTAATGGTCAGT | 20840 |
rs49486321 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111675127 | TTTCTGTATAGTGAC[C/T]GGTTGGAACCAGGAG | 20840 |
rs49490749 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111635937 | AACTAGATCATTTCT[C/T]TCTTGCCTATGGGAC | 20840 |
rs49498600 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111653789 | ATTAAAACGAAAGGA[A/G]CACGTAAAATGCCAG | 20840 |
rs49513141 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111628401 | TCCTGCAAGTCTCTG[A/G]CCATTCTCACCCAAC | 20840 |
rs49513726 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111628231 | TACTGCTTAAGGCGG[A/C]TTCTATTTGACATAT | 20840 |
rs49517838 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111665767 | TTTTAGCGTTATTGT[C/T]CATTTTTACTGCTGG | 20840 |
rs49522295 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111629681 | TTTCATCAATGTAAC[A/G]CTTAAGGTTAACTAG | 20840 |
rs49526908 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111584386 | GAGGAACTTTCTTCA[C/T]GCTCATGGTTAGAGA | 20840 |
rs49528903 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111643311 | TTGATTTGGAAAAGG[A/G]ACATGTTTTTCCTCC | 20840 |
rs49529962 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111566569 | TTCCTCCACAACTTG[C/T]TTCTTGGTCATGATG | 20840 |
rs49536218 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Stac | Mm_Celera | 9:111562162 | TCCTGCCAGCCAAAC[C/T]GAGACACAAACTGAG | 20840 |
rs49547711 | snp | A/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111570734 | TCAGTGTCCCACCTG[A/G]CCTCTACAGCATCAG | 20840 |
rs49547881 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111633258 | AGTGGGTGGGAGCTC[C/T]GAGAAGGAGCTGCAT | 20840 |
rs49561468 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111649908 | GTGATAAAAGTCCCT[A/T]TACATTTGGAAGTGG | 20840 |
rs49566289 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Stac, Gm36034 | Mm_Celera | 9:111593819 | ACAGGAGTTTTGTGT[A/G]GCTCGTAGCCATGTT | 20840 |
rs49569548 | snp | C/G | | | intron-variant | Stac | GRCm38.p3 | 9:111627561 | CCTCTCTACGTGGGA[C/G]CTAGGGACTGAAATT | 20840 |
rs49569986 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111646610 | CTATCCAGTCTGTGG[A/C]ATTTTTATTACAGCA | 20840 |
rs49583850 | snp | A/G | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111611480 | GCAAGTGTAGTTCTG[A/G]TGGCCGGAGAGATGA | 20840 |
rs49590980 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Stac | Mm_Celera | 9:111636573 | AGGTGGGCTCCTTTG[A/G]TTAAGTATTCATCTG | 20840 |
rs49594762 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111640537 | GAGTGGCAATAACTA[A/G]TCTCAAGACATTGCT | 20840 |
rs49605807 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111646762 | GTCTACCACACACTC[A/G]CCCAGAGTACAGCCT | 20840 |
rs49606530 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111627184 | CTAAGTCATGTGTGC[A/T]AGAGAGAGAGACATG | 20840 |
rs49637212 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111651479 | CAGAAATGGCCCTGA[A/G]TTCCTGCTATGGATA | 20840 |
rs49638046 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Stac | Mm_Celera | 9:111609308 | AGGTGGCTAACAGAA[C/T]GGTGTCATAAAAGAG | 20840 |
rs49638577 | snp | A/C | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111629369 | AGAAACATGGTGTCT[A/C]GTGAAAAAATGAAAA | 20840 |
rs49644189 | snp | G/T | | | intron-variant | Stac | GRCm38.p3 | 9:111686674 | ACTGGGTGGCTCCAC[G/T]GATGAAGGCTCTTGC | 20840 |
rs49644569 | snp | C/G | | | intron-variant | Stac | GRCm38.p3 | 9:111639376 | ATGCCAGTATTTATT[C/G]AGTGGCAGAAGCCAG | 20840 |
rs49653982 | snp | A/C/T | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111660584 | TGAAGGGCAAGCAGA[A/C/T]CCCAGCTCTCTAAGC | 20840 |
rs49663095 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111642230 | CTGGATGAGAGACTA[A/G]CTTACAGATGGAAGA | 20840 |
rs49682331 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111641772 | GCTGTTGAGCTTTGC[C/T]CTTGAGAAGGGGTGG | 20840 |
rs49682813 | snp | C/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571653 | GTATTGGTGGGGGCC[C/G]GCCCAGAGTAAAAAC | 20840 |
rs49685956 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111610387 | TTAATAAAAACAGGG[C/T]AAACAAGCCAGGAAG | 20840 |
rs49697481 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111658254 | TAAGACTTGGGTTTT[C/T]CATCTTTATTTGCTG | 20840 |
rs49710924 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Stac | Mm_Celera | 9:111646759 | GCTGTCTACCACACA[C/T]TCGCCCAGAGTACAG | 20840 |
rs49711283 | snp | C/G | | | intron-variant | Stac | Mm_Celera | 9:111646127 | TACAGGCACTGGTGT[C/G]CAAGTTCCCATCTCC | 20840 |
rs49721543 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | Mm_Celera | 9:111669081 | ACAGAGAGGAAACAT[A/G]TTTCAAGATGCTGAG | 20840 |
rs49722571 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Stac | Mm_Celera | 9:111645889 | TTGTAAATAGTAGGG[A/G]CTGATCACAGTCTGA | 20840 |
rs49725663 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111656457 | ACAGGTAGTGCTTAA[A/C]AGATAGCTGCTGCCC | 20840 |
rs49726066 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111627284 | GATAGTTACCATCTC[A/C]TTACGGTGACTGTCA | 20840 |
rs49727228 | snp | C/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111656212 | GTACTTCAGCCATGA[C/G]CAGACAGCAGGGTCT | 20840 |
rs49727377 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111610240 | GATGTCACTGGATTT[C/T]AAGTAAGCAGTATTG | 20840 |
rs49727629 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Stac | GRCm38.p3 | 9:111685806 | AGAACTCTAGACCAG[A/T]GGGTCTGCTGTATCC | 20840 |
rs49733186 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Stac | GRCm38.p3 | 9:111679282 | TAAATGAACAGAGGA[A/G]AGCATAGCTAAATTT | 20840 |
rs49749938 | snp | A/C | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111569823 | CATTGCAGAACATGG[A/C]ATTATAGCATGCACG | 20840 |
rs49752762 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111643102 | CCTGCGAGGCATACA[A/G]TTCCTGTGGGCACTC | 20840 |
rs49761044 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Stac | Mm_Celera | 9:111634306 | TTCCTGGGACCATGG[C/T]CACTAATATTTGACG | 20840 |
rs49767888 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111610397 | CAGGGTAAACAAGCC[A/G]GGAAGTGGTGGCACA | 20840 |
rs49773201 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111639228 | GCTGACAGGATGACC[A/T]GCTCAGATACCCCTC | 20840 |
rs49774794 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111638092 | AACCAACACAGGAGC[A/G]TAGGCCAGGACGGTG | 20840 |
rs49776477 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111658609 | GCCCTTAGCACAGAT[A/C]CTGGGACAGAGTGTC | 20840 |
rs49776639 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111645642 | GGAAACTGAGGAGGG[A/C]TCAATTTTGGGACCA | 20840 |
rs49784182 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Stac | GRCm38.p3 | 9:111634327 | ATATTTGACGTTAGA[A/C]GAAACTGTCTCTTAG | 20840 |
rs49791392 | snp | C/T | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111609062 | TTTGGATCACTGCAG[C/T]CGTCCTGGTTTAGCC | 20840 |
rs49806207 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111648187 | TCACTCTTGTTCTTC[A/G]TTCTTTTCATCATGC | 20840 |
rs49814916 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111651624 | GGGCAATGTAAAAGG[A/G]GAGATGTCTTGGAAG | 20840 |
rs49815046 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111687948 | TTAGACATCTATCTT[C/T]TTGCTTATATTGGGA | 20840 |
rs49830999 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111634212 | TGCTGACCACACCCA[C/T]ATATTTGAAAAAAAA | 20840 |
rs49831055 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111674867 | TTAAGATACAAGCTT[C/T]AAGAGCAGTGGAAAT | 20840 |
rs49832198 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111608403 | TCCCCTAAGAAAGTA[A/C]CATTTAACCGAGAAC | 20840 |
rs49841456 | snp | A/T | | | intron-variant | Stac | Mm_Celera | 9:111645223 | GGGAAGGGTAAAAGG[A/T]GGCAAACTTAGTAGT | 20840 |
rs49848050 | snp | A/C | | | intron-variant | Stac | GRCm38.p3 | 9:111633952 | GAGGCGGATTGATTA[A/C]AACTTCCATCATCTC | 20840 |
rs49848669 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111671253 | ACTGCTCTAGCAAGC[A/G]GAGGAAGGTACCTTC | 20840 |
rs49875124 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111634086 | ACTTGGAGGTAAAGA[C/G]CTCTCAGAATATATG | 20840 |
rs49886447 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111639967 | GAGCAGCAAGGGCTC[G/T]TAACCACCCAACCAT | 20840 |
rs49886576 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111627554 | CATCTGTCCTCTCTA[C/T]GTGGGAGCTAGGGAC | 20840 |
rs49890817 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111676007 | AGCTTAATTGTTAAC[A/G]TGACCCTGGAGTGTG | 20840 |
rs49898706 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111653845 | GGAAATAAACACAGC[A/G]AATGCTAATGGGTAA | 20840 |
rs49901340 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111631476 | GTGCCTCTTCAAAGC[C/T]GTAATTTTCTACTGT | 20840 |
rs49906351 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111664833 | GGTGGTCTGGGGGTT[A/G]CCCAGTAACAAGTGA | 20840 |
rs49910993 | snp | A/G | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111640076 | GGAAACTTTATCCAT[A/G]TATGTACTCACTTGG | 20840 |
rs49922338 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641692 | AGCATTTGTTTGTGG[A/G]GAATTTTGTTTAAAT | 20840 |
rs49930759 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111665717 | TTTGTAGTTGACAAA[C/T]GTTACCATGATTTCT | 20840 |
rs49934998 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111577151 | AGTCAGAAAAATGAT[C/G]TTCATGTCTTGACCT | 20840 |
rs49943645 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Stac | GRCm38.p3 | 9:111666635 | CGTTCTGACTAGAAT[C/G]ATCAGAGTTAGGGAG | 20840 |
rs49943871 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111655215 | CAGGTGCCGATTCCT[C/T]ACCCCATAATTAAAA | 20840 |
rs49948009 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111583709 | GACATGACACAGCCA[C/T]TGAATATGTATTTGA | 20840 |
rs49950760 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Stac | GRCm38.p3 | 9:111656128 | CAGTCAGAATGACAA[A/G]GTCCTCTCTAAGAAA | 20840 |
rs49961997 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111652103 | TGGTAAGGTGAGAGG[C/T]TTCCTGGGATGAGTA | 20840 |
rs49971033 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111584086 | AAGGAACACTGAGAT[A/C]TGACTGAGAGGATGA | 20840 |
rs49975987 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111630295 | AAGATCTACTTGGAG[A/G]ACAATGTGAAGTTGC | 20840 |
rs49979196 | snp | A/T | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111616426 | GGTATCGAATGTGCT[A/T]TCTGCCAATCATGGT | 20840 |
rs49982626 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111645837 | AATAAACATGTACAC[C/T]ATGTTCAAAGCTAAG | 20840 |
rs49982877 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111669979 | ACTGCAATTGTCTCC[A/G]TGCCAGCTGGATAAA | 20840 |
rs49987296 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111670043 | AGAGCCCTTATGCAT[C/T]GAGGAGATGGTTTTA | 20840 |
rs49989340 | snp | A/G | 0.391111 | 0.206368 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577939 | GACAAGATCTAGTGG[A/G]TGTGGTATGCTCTGT | 20840 |
rs49997276 | snp | C/G | | | intron-variant | Stac | GRCm38.p3 | 9:111610094 | AAAGGAGAGAACTGA[C/G]TTTTGCAGTTGTCCT | 20840 |
rs49998641 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111657497 | TATCTCTGTATCTGT[C/T]GTATCACTGAGAACA | 20840 |
rs50000536 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111643358 | CTAAAATAGTTTACA[C/T]CTTCTTGTTGAAATA | 20840 |
rs50006629 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Stac | Mm_Celera | 9:111646810 | GAAAACACGGAGGCT[A/G]TCTTAGGCATGTCTA | 20840 |
rs50024974 | snp | G/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111571219 | CAGAAGGACACCCTT[G/T]CTGTGCTGGAGGGAC | 20840 |
rs50025794 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111657542 | ATTCACATTTAAACC[C/T]GGCAATAAACAATTC | 20840 |
rs50028373 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111645665 | TGGGACCAATCATTT[C/T]TCTTCAAGAGAAAAG | 20840 |
rs50028655 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | Mm_Celera | 9:111623779 | AAAAACTTATGATCA[A/G]AATGTTTATTAGAGG | 20840 |
rs50050729 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111570437 | AAAAGTCATTTGGAG[C/T]CACATATAGGAAAGA | 20840 |
rs50063752 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111640457 | TGACATTTGAGCAGA[G/T]ATGTGAAGAAAGTGG | 20840 |
rs50068767 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111652143 | GGACTTAGGTCTAGC[A/T]GCAGAGATCACCATG | 20840 |
rs50086838 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111671588 | TAGCTCTTTCTCCCC[C/T]CCTTAAATTTTAACT | 20840 |
rs50087248 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111563596 | CCTGAGTACACAGTG[C/T]CAGTCTTTGTGGTGG | 20840 |
rs50111012 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111652966 | GGAGAAGTGAATAGC[C/T]TTTATAGGGTGCTGG | 20840 |
rs50130310 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Stac | Mm_Celera | 9:111584443 | ACATGTGGGGTCATG[C/T]CACTGCATGAGTGAC | 20840 |
rs50130946 | snp | A/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571892 | CTTTGAGGCTTTATC[A/G]GTTATTCCCACTTCC | 20840 |
rs50133249 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111687572 | GGCTCAGTGGGTAAC[A/G]ACACTTGCCACGAGC | 20840 |
rs50133596 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Stac | GRCm38.p3 | 9:111569625 | GAGGTCTGGGTCTGA[C/T]TTCTCTGTCCTGTCT | 20840 |
rs50139364 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111618339 | AGAAACCAAACAGGG[C/T]ACGTATTACTGTTTT | 20840 |
rs50160048 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111630574 | ATCGAGGAAAGGAAT[G/T]TAGAGCCAGGGATTG | 20840 |
rs50162674 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | Mm_Celera | 9:111563587 | CAGACCTGGCCTGAG[C/T]ACACAGTGCCAGTCT | 20840 |
rs50165898 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111629888 | AAGATGGAGAGTGAA[G/T]ATATGCCGCCTTGAC | 20840 |
rs50167532 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111640782 | CAGACATTTATTGGA[C/T]GGGCTGCTCTAGGGA | 20840 |
rs50194452 | snp | G/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Stac, Gm36034 | Mm_Celera | 9:111596108 | CCTACTTATGCATGA[G/T]ACTACACCAGCTTAC | 20840 |
rs50200743 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111640183 | ACCTTGCAGGGAGGG[C/T]GTCATTCATCACTCA | 20840 |
rs50201075 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111669368 | AAGCAATGTAGAGCC[A/G]TTTTGTTAATGATTC | 20840 |
rs50218139 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Stac | Mm_Celera | 9:111671408 | CTTACTCTGTGGGTA[A/C]AGCCCCTACAGAGTG | 20840 |
rs50221651 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111628183 | GGGCCAAGGAGTTTA[C/T]CCTTTCAAAGCGATG | 20840 |
rs50224588 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111649329 | GAATGCACGTTTGCT[A/G]CTTATGCTCAGATTT | 20840 |
rs50225215 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Stac | Mm_Celera | 9:111562348 | GACCACACCATGACC[C/T]GGAGCAGACTCCAGC | 20840 |
rs50232418 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stac | Mm_Celera | 9:111647051 | CCAGATTTACTGGGA[A/G]GGCGATCACAGAGTT | 20840 |
rs50238044 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111641023 | GAGTGAACAGAGGCA[C/T]GCCCTTTTACTAGAA | 20840 |
rs50247409 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111627848 | CTGCATGTTATCAAA[G/T]CTGATCTCGTCTTTG | 20840 |
rs50247779 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Stac | Mm_Celera | 9:111643458 | CATGAAGGGAATAAG[G/T]TACTTGGCAAGCATA | 20840 |
rs50258597 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111629431 | TGATGGAGTGGACCC[A/G]TGCCTGAGGTTAGTC | 20840 |
rs50265755 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111669323 | CTCTATCAGGGTCTT[C/T]AGGTAGATTTCTGTA | 20840 |
rs50273357 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111631967 | TTATAAAACCAGCTA[C/T]GGTGGCACACAAATG | 20840 |
rs50273955 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111686595 | TGCCTCTGACTCAGA[A/G]TGCTGGGATCAAAGA | 20840 |
rs50301021 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111637884 | ACTGTGCAAAACAAG[G/T]CTCCTTCACCCAGGG | 20840 |
rs50318387 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111674259 | GAGTTCCTGGCAGCT[A/G]CATCCCTGTGTAAAG | 20840 |
rs50319888 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111654404 | CACCAAATAAGATGC[A/G]TTGCATTGACCCACT | 20840 |
rs50327742 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111641749 | TCTGATGTTGCCTAA[C/T]AGGTCTGGCTGTTGA | 20840 |
rs50328420 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | GRCm38.p3 | 9:111667396 | ACTGAGCCTCTATGC[C/T]TCCAAACTTCCCTCA | 20840 |
rs50338311 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111611487 | TAGTTCTGGTGGCCG[G/T]AGAGATGAATCCTTA | 20840 |
rs50350687 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Stac | GRCm38.p3 | 9:111687024 | TCTTTAGACCATCAG[A/G]ATGATGTGAGCACTG | 20840 |
rs50353707 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111619726 | TCCTAATGTCCTTTC[C/T]CTCTTTCAGACTTGT | 20840 |
rs50355110 | snp | A/C | | | intron-variant | Stac | Mm_Celera | 9:111570496 | TATTTTAGAACAATA[A/C]ATCAGTTATAATTAT | 20840 |
rs50357657 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111633753 | TTGTTTAGACGAAGA[A/G]CAGGCATAGTTGGGA | 20840 |
rs50359430 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111633932 | TGTACTTCATAACAC[C/T]CTCTGAGGCGGATTG | 20840 |
rs50366509 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111625481 | GGGCGCCCATCACTA[A/T]CAACTGGATAGGACA | 20840 |
rs50368009 | snp | G/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571893 | TTTGAGGCTTTATCG[G/T]TTATTCCCACTTCCT | 20840 |
rs50369467 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Stac | GRCm38.p3 | 9:111673937 | TGATGATGACGTCGG[A/G]TGGAAGAGCTTGAAA | 20840 |
rs50371027 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111656344 | TCTTGTTTGTGTCTT[A/G]TCTAGGCTCCTCTTG | 20840 |
rs50371576 | snp | A/T | | | intron-variant | Stac | Mm_Celera | 9:111646778 | CCCAGAGTACAGCCT[A/T]CTAGGTAACAAGAAT | 20840 |
rs50373898 | snp | C/T | 0.18 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111681818 | GACTTGAGTTTCATG[C/T]CCAGAATCCATTCAA | 20840 |
rs50384968 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111672064 | TCAGACGAGTTCATG[C/G]AATTCAGGCATGGAG | 20840 |
rs50386994 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111628822 | ATTTATCACACTGGT[A/G]CAGTGATTACTGGTT | 20840 |
rs50408936 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111584413 | GAGACTCAGACAGCT[C/T]GTGTAGCTCTCTAGA | 20840 |
rs50410328 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Stac | GRCm38.p3 | 9:111664788 | TCTCATCACAGGGTT[C/T]TGTGATTAACCACCA | 20840 |
rs50410499 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Stac | Mm_Celera | 9:111637996 | ATGCAGATTATGCAC[C/T]CTGCTCCCCACCAGA | 20840 |
rs50417495 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111627611 | GAAAGCATTCAATGA[C/T]GGGTGAACTCTCCAG | 20840 |
rs50432412 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111563137 | GCCAAGGGACAGTTT[C/T]GTTATTAGCTCCAGG | 20840 |
rs50438995 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111569438 | GTGCTGAGGGCAAGG[C/T]GGCGTGGCCTGCAAT | 20840 |
rs50440422 | snp | G/T | | | intron-variant | Stac | GRCm38.p3 | 9:111639363 | GAGTCTCAGTGAGAT[G/T]CCAGTATTTATTGAG | 20840 |
rs50448903 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111673285 | CCTCCTGATTCACAC[A/C]TGGCTGCTTTGCACT | 20840 |
rs50465327 | snp | A/C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111685493 | GTTAATAAGCAGGGA[A/C/T]GGTTAGCTAGTTAGA | 20840 |
rs50492254 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111583862 | GATAAGAATAAGAAG[C/T]GATGACTTCAAGCCT | 20840 |
rs50493477 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | Mm_Celera | 9:111633983 | AGAGAGCTAAACTAC[C/T]GTAGGTCCAGAGGCA | 20840 |
rs50501650 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111652477 | AAGGAGAAGCTAACT[A/G]ATGTGATAGAAGTCA | 20840 |
rs50508161 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Stac | Mm_Celera | 9:111633872 | CCTTCCCACTGAGAA[C/T]CGCCCACTTGGGAAC | 20840 |
rs50516059 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111671944 | ATTGGCGTTTGATTA[G/T]CAGCTGTGTACAGAA | 20840 |
rs50526182 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111637400 | ACTAAGTTACATGTT[C/T]ATTATCTATTCTAGA | 20840 |
rs50539368 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111688417 | AGATCTGAATGGTAA[C/G]CTGGATAAATTGGTG | 20840 |
rs50549344 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111667310 | AACAAATTAACCGGG[A/C]CCCAGAGCCAGAAAT | 20840 |
rs50567116 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111648053 | TTCCTGCAAAGAGGC[C/T]CTCAGTGGTTTTCGA | 20840 |
rs50581009 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111670103 | GTGTACATCAGGCAT[A/G]CAGCATTGATGTTCA | 20840 |
rs50583043 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111633811 | GCCTTATCTGAAAAC[A/G]TAGGCAGGCCTCATG | 20840 |
rs50592655 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111648131 | CACACCCCTTCAGTG[C/T]CCAGCAAGGCCTGGC | 20840 |
rs50599311 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111646179 | TCACACACTTGTAAT[A/G]CCAGCACTTGGAGAA | 20840 |
rs50619562 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Stac | Mm_Celera | 9:111635886 | TTAGCTCTCCTGGCC[C/T]TTCAGGTGTCCTTGC | 20840 |
rs50623379 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | Mm_Celera | 9:111581836 | TGAAGTTGGGATACA[C/T]AACTACATTGTCTAA | 20840 |
rs50631065 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111652383 | GACAAAGGACCGCCG[A/G]TAAGCAGAAAAAGCC | 20840 |
rs50632929 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111685968 | CTTGGTTTTGAGGTG[C/T]GATGGATTGAATTCA | 20840 |
rs50634811 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111576896 | GCTAGGGATGGTACA[A/G]CCTGACTATGTGGAA | 20840 |
rs50650386 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111673230 | GAATCCCAGAAACTT[C/T]TCTCTAGGTCGCATC | 20840 |
rs50654745 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111687885 | TCCATGTGATGTTTT[C/T]TTGATATATGGAGTA | 20840 |
rs50661580 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111640635 | GAAACCAACCTTCCC[A/G]CAGCAACCAATGAGG | 20840 |
rs50667708 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Stac | GRCm38.p3 | 9:111687452 | CAGGGTCTCATGCTG[C/T]AGCTCTCCTGCCTCT | 20840 |
rs50699345 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Stac | Mm_Celera | 9:111632494 | AAAAGATTACCCTAA[C/T]TGGAGATACTTAGGC | 20840 |
rs50703619 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Stac | Mm_Celera | 9:111632445 | TATTGTGTGTACACA[A/T]GATTATTAAACATGT | 20840 |
rs50708930 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111652066 | GGGAATTTTAGAATG[C/G/T]CTGGGTAGAAGAATC | 20840 |
rs50716734 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Stac | GRCm38.p3 | 9:111567668 | ACTAGTATACTGACT[C/G]TTCTGATGACATTTA | 20840 |
rs50720529 | snp | C/T | 0.391111 | 0.206368 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111578441 | CTAGCTGCAGGATAT[C/T]GAGTGCCTTTAACAC | 20840 |
rs50729925 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641752 | GATGTTGCCTAACAG[A/G]TCTGGCTGTTGAGCT | 20840 |
rs50730438 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111674190 | GGTCATTAGCAGATG[C/T]GAGACCCATGTGGTG | 20840 |
rs50758537 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111639975 | AGGGCTCGTAACCAC[C/T]CAACCATACAGTTTG | 20840 |
rs50764984 | snp | A/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571481 | GATTTTTTCCTCTGT[A/G]TTTTGTCTCTGTCTT | 20840 |
rs50790570 | snp | C/T | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111637870 | TGATAACCTGAGAGA[C/T]TGTGCAAAACAAGTC | 20840 |
rs50800206 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111673689 | GTGTTCAGATGGGAT[A/G]CAGCACTCTCTGATC | 20840 |
rs50801645 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111652366 | CAAGCATTCTGAATA[C/T]TGACAAAGGACCGCC | 20840 |
rs50803068 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111628358 | TCAGCCCTGAGGACA[C/T]GCAGACTTTACATTT | 20840 |
rs50806094 | snp | C/G | | | intron-variant | Stac | Mm_Celera | 9:111639164 | GTAGAGCTGGCCCTG[C/G]TTGCAGGGGTTGCTG | 20840 |
rs50807241 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111643589 | TAGCTGAGGCTGTGG[C/T]TTGTCAGAGTCTTTC | 20840 |
rs50814138 | snp | C/G | | | intron-variant | Stac | Mm_Celera | 9:111649880 | CAGGTAAAGGGCTCA[C/G]TAAGCACTTTCAGTG | 20840 |
rs50819605 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111674721 | TCCTCACGACTGTCT[A/T]GTATGGCTTTTGGCT | 20840 |
rs50831342 | snp | A/G | 0.391111 | 0.206368 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111578153 | CAGACTCTAGTCTTT[A/G]GGATAATTCAGAACT | 20840 |
rs50834560 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111664542 | GCTATTCTTAGGTGT[A/G]TCATCCCTGGTGTGA | 20840 |
rs50836059 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111683809 | GCTGTGTTAGTGCTA[C/G]CTGAAATAGCTTCAG | 20840 |
rs50839614 | snp | C/T | | | upstream-variant-2KB | Stac | GRCm38.p3 | 9:111692021 | CAGGGCCAAGGGAGT[C/T]TTCCACAAGAGTGAA | 20840 |
rs50842269 | snp | A/C/G | | | intron-variant | Stac | GRCm38.p3 | 9:111644221 | CAAAAATTTCCCCCC[A/C/G]TTGTATTAATGAAGA | 20840 |
rs50847235 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111666920 | CTGCATCTATAAAGT[A/G]AGCATGAAACAAGTA | 20840 |
rs50848710 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111650341 | ATGCTTGCCCTCATC[C/T]GGATTTGAGAACATC | 20840 |
rs50857214 | snp | A/C | 0.32 | 0.24 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577116 | CAGGAGGACTGGGCT[A/C]TCTTTGTCTTGTATT | 20840 |
rs50871720 | snp | A/C | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111616135 | CTCCATGTGGAACCT[A/C]ATGCTTAGATCAGGT | 20840 |
rs50878916 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111674773 | TTTCTATGGATGAGC[A/G]CACAGAAATTGAGGT | 20840 |
rs50881937 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641856 | GGTTGGTGCTTATTG[A/G]ATACAAATCTTTCAT | 20840 |
rs50910071 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111648014 | CTGCCTATGTCCAGG[A/G]ATTACATTCTGTTTT | 20840 |
rs50914853 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111644973 | TCTCCTAAGTATGAT[A/G]TCATCAGGGTCATGC | 20840 |
rs50916216 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111642221 | TGTCAAGAACTGGAT[A/G]AGAGACTAACTTACA | 20840 |
rs50917908 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Stac | GRCm38.p3 | 9:111664455 | TCACCACACCCAGAT[C/T]CTTAGAGATTCTTCA | 20840 |
rs50923896 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111644585 | AGGCGCTGGGAGAGC[A/G]CGAAGAGTCAGAAAC | 20840 |
rs50936598 | snp | A/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111629287 | ATTAAATCTGAATCC[A/T]CTTAATATGCTATAT | 20840 |
rs50937228 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111674293 | ACCACTGGGCTGCTT[C/T]CCATGGTCCCAAAGT | 20840 |
rs50938941 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Stac | Mm_Celera | 9:111562335 | AACTTCTCACTAGGA[C/T]CACACCATGACCTGG | 20840 |
rs50939851 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111685183 | AAGGTATACATGCTT[C/T]TCCCAGATAACACAT | 20840 |
rs50944538 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111680470 | TCTAAGAGACAGATG[A/G]TCAAGGACGCTCGCA | 20840 |
rs50953329 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111664594 | TTTTAAAGTTTGATC[A/G]CATAGTATGGAATTG | 20840 |
rs50973162 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111641838 | ATACAAGCAAGCCAG[C/T]AGGGTTGGTGCTTAT | 20840 |
rs50973185 | snp | C/T | 0.142012 | 0.225474 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111574891 | TGCCATCTCGACAGT[C/T]GCAGCTGCCTGCTGA | 20840 |
rs50977259 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111606053 | CACACATCTTGCAAG[C/T]GCTGCCCATCTTTGT | 20840 |
rs50977479 | snp | G/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111647660 | AGCAAGGCTTGGAAT[G/T]GGAGCTTGGTGGTCT | 20840 |
rs50991615 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111660562 | AAAAGGAGGAGGAAT[A/G]CACAGATGAAGGGCA | 20840 |
rs51019880 | snp | A/G | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111578197 | GCCTTTGTTTGTGTA[A/G]ACCCAGTCTCCTTTC | 20840 |
rs51037621 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111620135 | CTGCTTTCTCTGGCA[A/G]TGTTTTCTGTTAGTC | 20840 |
rs51037767 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111619279 | AGCCATCGCTCCCTG[A/C]CTATGTTACCCACTC | 20840 |
rs51037875 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111578466 | TAACACTATTCATGG[C/T]TTATCAAAATGCAGG | 20840 |
rs51040327 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111581741 | CAAGGCTTCATGAGC[G/T]TAGTCGGCAGACCAC | 20840 |
rs51040439 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111664772 | GAAAGCATCATTCCC[A/G]TCTCATCACAGGGTT | 20840 |
rs51041090 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111627043 | TGCTTTCTTCTTTTA[C/T]CTGAAAGGTATAGAG | 20840 |
rs51048951 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111643283 | TCTGAATTTTCCTAC[A/G]TGATCTACATCTTTG | 20840 |
rs51052367 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111683933 | ATGAGCGCTTCATCT[C/T]TTCCTTTAGTCCTCA | 20840 |
rs51063174 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Stac | Mm_Celera | 9:111644886 | TTGTTTTTTTCTGCA[A/G]TGACTCCTGGGTATG | 20840 |
rs51064955 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111655046 | TTATTTACTAGGCTT[C/T]TAGGGACCTGGGACT | 20840 |
rs51065589 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111652935 | AGAATGTAATTAAAT[A/G]GCACAGTTGTAATGG | 20840 |
rs51068653 | snp | G/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111623203 | TAAGATGATCTTCCT[G/T]CTAGAATTTATGGGA | 20840 |
rs51081957 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111564527 | TCTACAAAGAGGCAC[A/G]CTCTGAAGAACACAG | 20840 |
rs51083327 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111650937 | GCATGAGCCACCGTG[A/T]GTGGAGAGGTGGAAC | 20840 |
rs51087273 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Stac | Mm_Celera | 9:111679728 | TTCAGCCATACACCA[C/T]GATGCCTAATTACTT | 20840 |
rs51088109 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111563107 | AGTATAGCATGCCGA[A/G]GACAACACCAGAAAG | 20840 |
rs51089584 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111672820 | TGATCACTGCACAGT[A/T]AATTAGAAGGTCCAC | 20840 |
rs51090940 | snp | C/G | | | intron-variant | Stac | Mm_Celera | 9:111645290 | GATGGAGTGTGTACT[C/G]TAAAATTGCCCCCCC | 20840 |
rs51091794 | snp | A/T | | | intron-variant | Stac | GRCm38.p3 | 9:111605896 | TCTTGGAAAGACAGA[A/T]GGGAAAAGATGTGAC | 20840 |
rs51102891 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111562813 | GCTACTGCCTGAGAA[A/C]GCAGTGCCACTCAGC | 20840 |
rs51108882 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111675301 | TGAATGCCCACCAGG[C/T]TTCTTCTAGAGCTAA | 20840 |
rs51116860 | snp | G/T | | | intron-variant | Stac | GRCm38.p3 | 9:111628943 | CCACCTTTCTCCCAT[G/T]ACAGCCACGGCCAGT | 20840 |
rs51134506 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Stac | Mm_Celera | 9:111623264 | GTGGGAGTCCCCAGC[C/T]CATGGATACTGCGAT | 20840 |
rs51150762 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111689668 | TGCAAAAGAGTACCC[C/T]TAGGCTGTGTCGGTC | 20840 |
rs51161228 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111675281 | AACGAAGGCTGTGCT[A/C]AGGGTGAATGCCCAC | 20840 |
rs51163480 | snp | A/C | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111628205 | AAAGCGATGGCATTC[A/C]GGAAACATACTACTG | 20840 |
rs51167822 | snp | A/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111571254 | GGACACCCTCTCTGT[A/G]CTGGAGGGAGACATC | 20840 |
rs51170266 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111652826 | CATTGTCTTCAGGGG[A/G]CATTATGTGTCACCC | 20840 |
rs51192054 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111640769 | GAGGTGATGATGGCA[A/G]ACATTTATTGGATGG | 20840 |
rs51197077 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111570302 | TATGCAGTTCAGCCT[A/G]GCTTTTAACTCACTA | 20840 |
rs51229353 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111641056 | GCATCAGAGAAGACA[C/T]GTTGTCATGGAGACC | 20840 |
rs51236471 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111660238 | GGGTTCTTTCTGTCA[C/T]CATCTTTGACTTCTT | 20840 |
rs51252493 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111677196 | AAGCCAATTTCACAC[A/G]TGCTTCTGTATGACA | 20840 |
rs51253961 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111652209 | CCGCTACTATGTGAG[C/T]GTCTCATGAGAATGT | 20840 |
rs51262032 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Stac | Mm_Celera | 9:111668869 | GAACAACTCTAGGCT[G/T]TTCCAGACACAGGGT | 20840 |
rs51265298 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Stac | Mm_Celera | 9:111687745 | AAAAAAAACCCTAAA[C/T]GTCCAAAAAAGGCCA | 20840 |
rs51270147 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111654371 | GCTCAATTTTAGACA[C/T]ATAAAGAAACCCATA | 20840 |
rs51273705 | snp | A/C | | | intron-variant | Stac | GRCm38.p3 | 9:111641428 | gagaaggatgaaaag[A/C]caatggagtcaaata | 20840 |
rs51280515 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111644839 | TAGCACCACACCAGA[A/G]ATCTCCAAAGATGTG | 20840 |
rs51282519 | snp | C/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111570698 | CCACATGTTGACTAG[C/G]AACTCTAGATCACAG | 20840 |
rs51284851 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111583058 | TTCCCTCCCAGCACC[A/G]TGACCCCTTAAGCTC | 20840 |
rs51292216 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111687693 | TGTAATAAGCGCATA[C/T]GCACATGCATACTTA | 20840 |
rs51308286 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111673422 | AAGAGCTCCCAGGCC[C/T]TTCTGCCCACACGGA | 20840 |
rs51308336 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111610247 | CTGGATTTCAAGTAA[A/G]CAGTATTGGATTGGG | 20840 |
rs51308643 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Stac | Mm_Celera | 9:111561477 | AGTGGCAAAATAAAT[C/T]GAAGCAACAATAATC | 20840 |
rs51311010 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Stac | GRCm38.p3 | 9:111628470 | GCATGTTTTGTGTTT[G/T]TGTATGTATGTCTTT | 20840 |
rs51318619 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641162 | GGAGGAAGGTCTGAG[A/G]TGGAGAGTGAGTGGG | 20840 |
rs51323536 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111676349 | GAGCTGCTATAACTA[C/T]CCCCACACTAATATC | 20840 |
rs51333297 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111666594 | TTGATCCTGTGAGCC[A/G]CCTGGTGAGTTTTCT | 20840 |
rs51334452 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111563549 | AATTTCTTCTTGACC[A/G]GGCCAGCACAGTTAC | 20840 |
rs51345035 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111651370 | CTACTAACTTTGAAC[A/C]TTTAAACACACTTGA | 20840 |
rs51347173 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Stac | Mm_Celera | 9:111608881 | CTATGCATTTCCTTC[C/T]GCTGACTTCAGTTTT | 20840 |
rs51352373 | snp | C/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111570793 | CTGGCACAATCTCCA[C/T]ACACATACAATAAAA | 20840 |
rs51361036 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111655967 | GCTTACAAAGCAAGA[C/T]AGACCACAGAACACC | 20840 |
rs51364717 | snp | C/T | | | upstream-variant-2KB | Stac | GRCm38.p3 | 9:111692043 | AAGAGTGAAACTTCC[C/T]GGGTCTTCTATAGAG | 20840 |
rs51364792 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111658231 | TGAATTCCATATACT[A/G]ACTCTAATAAGACTT | 20840 |
rs51371074 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Stac | Mm_Celera | 9:111636120 | TCTTAGGCATAAAGA[C/G]CAGCTTTGGCTGAAT | 20840 |
rs51373164 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111640835 | GGAGGCAAGATTGAG[A/G]TAAGGAGACCTGCTG | 20840 |
rs51375922 | snp | A/T | | | intron-variant | Stac | Mm_Celera | 9:111686737 | GAACCCATGTGGTGG[A/T]GGGGGGGGGCAGGAC | 20840 |
rs51376114 | snp | A/T | 0.495868 | 0.0452663 | intron-variant | Stac | GRCm38.p3 | 9:111635460 | ACCAAGGCTGTGTGT[A/T]ATACTGTCTTCTCTC | 20840 |
rs51387636 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111686785 | CCTCAGATCTTCAAA[C/T]ATGTGCACCATGCTA | 20840 |
rs51388905 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111633408 | TGGTATTTCTCTACC[G/T]TCCTGATTGTCACAT | 20840 |
rs51391109 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111655146 | ACAGGGAATAGAAAC[C/T]AAGAAGCAAGGAGCA | 20840 |
rs51403626 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111677167 | GATATGACAGTCAAG[C/T]CTCTCCTCTGGTGAA | 20840 |
rs51404988 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111686765 | GACTGACTCCCAAAA[A/G]TTGTCCTCAGATCTT | 20840 |
rs51405467 | snp | A/T | | | intron-variant | Stac | Mm_Celera | 9:111636193 | AACTCTCAGATCACA[A/T]GGCCTGCAGAGTGAG | 20840 |
rs51415850 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111645339 | ATCATTAGCAATGTT[C/T]ACATTGGTCTTTGAG | 20840 |
rs51420647 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111660323 | AACAGCTTCTTCACC[A/G]TGTCTGCTCTTACTA | 20840 |
rs51423372 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111639755 | GCATAACCATTGAGG[C/T]AAGTTCTATTTAAAG | 20840 |
rs51423482 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111576679 | CTTGGCAGCCCTTGG[C/T]TCACAATCGTCCATT | 20840 |
rs51424488 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111654338 | AAATAAATGCCCCGA[A/G]CAAGGGATGTATTTT | 20840 |
rs51429521 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Stac | Mm_Celera | 9:111629189 | TGTAGAGAACTTGGA[C/T]AGTTATGAAAGCCAT | 20840 |
rs51438284 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111581757 | TAGTCGGCAGACCAC[A/G]GGCTTCCTGGGCTCC | 20840 |
rs51441739 | snp | C/G | | | intron-variant | Stac | GRCm38.p3 | 9:111569549 | CTGTCTGCGTCTCTG[C/G]TCTTTCATCTTTTAG | 20840 |
rs51452655 | snp | C/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111570662 | TGCTCTTCCAGAGGA[C/T]TCAGGTTCAATTCTC | 20840 |
rs51461647 | snp | C/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111572080 | TTAGTTATGGTGTTC[C/T]ATTATAATAATAAAA | 20840 |
rs51482570 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Stac | Mm_Celera | 9:111635258 | AGTAGTTCATCCTGT[A/G]TCCCATAAGCTAGTG | 20840 |
rs51483986 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111576272 | TATCTAGGATTTCCA[C/T]CCAATGCCTTTTCAG | 20840 |
rs51485818 | snp | G/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111658174 | ATCAGAGAGAGCTAT[G/T]CATGTCAACATGCAT | 20840 |
rs51489669 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Stac | Mm_Celera | 9:111561542 | GGAAGCAGGTCTGAA[C/T]GCTGGGACGGGGCTT | 20840 |
rs51490346 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111620360 | CATCAGTTGATGGGG[C/T]GGAGCCTTACTCTAC | 20840 |
rs51499099 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Stac | Mm_Celera | 9:111645465 | AGTCTAACCAGGGTC[A/T]GTTCGGTCTAAAAGG | 20840 |
rs51508586 | snp | A/C | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111573398 | CAGTCAATGTTACTG[A/C]AAACCCAGAGTCGGG | 20840 |
rs51510873 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111627318 | TGTACCCACCCCTCT[C/T]TTCACCCTGCCCCCC | 20840 |
rs51511586 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111641762 | AACAGGTCTGGCTGT[G/T]GAGCTTTGCCCTTGA | 20840 |
rs51515629 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111666303 | CTTCCACTTTACTGA[C/G]TCCATCTTTAGGTTT | 20840 |
rs51529653 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111647989 | AACCACTTCCCTTCT[C/T]CAGGGTCCTCTGCCT | 20840 |
rs51532141 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641012 | TGGGTGCAACTGAGT[A/G]AACAGAGGCATGCCC | 20840 |
rs51536075 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111655192 | CTTTTGATGGGCACA[C/T]GGAGAGCCAGGTGCC | 20840 |
rs51538136 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111569031 | TGGTGATTGGCTACC[C/T]TCCCCCGGGGGTCCC | 20840 |
rs51553073 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111685636 | CTCTTCTGTTACTAA[C/T]TTCAACCCTCTGTAA | 20840 |
rs51554782 | snp | C/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571823 | TGTTTGGAGAGGATA[C/T]AGGACCTTTAGTAGG | 20840 |
rs51556197 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Stac, Gm36034 | Mm_Celera | 9:111594186 | CTTTTTAATGCTGTC[A/T]TTATTCTGTCTTGAA | 20840 |
rs51568630 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111625469 | CATGATGTGCCAGGG[C/T]GCCCATCACTATCAA | 20840 |
rs51574781 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111631994 | AATGCAATCCCAGCT[C/T]TCTGATGGAGGAAAG | 20840 |
rs51577320 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Stac | Mm_Celera | 9:111668747 | TGCAGAAAAAAAAAA[A/G]GAATCAAATAAAGTA | 20840 |
rs51579806 | snp | C/T | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111612387 | ATTAGGAAGACTCAA[C/T]ATAATGTCAAAATTA | 20840 |
rs51580764 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stac | Mm_Celera | 9:111683886 | AAAGGAGAAGATCAC[C/T]GGTACTCTATGCATA | 20840 |
rs51588429 | snp | A/T | | | intron-variant | Stac | Mm_Celera | 9:111637345 | CTATCATATAAGGAC[A/T]TTTCATACACGTATG | 20840 |
rs51599055 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111581553 | CCTCATGAATTCTGT[G/T]CCTTGATTTGCCAGT | 20840 |
rs51600683 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111581771 | CGGGCTTCCTGGGCT[C/T]CAGGGTCAAACCTAG | 20840 |
rs51621843 | snp | C/G | | | intron-variant | Stac | Mm_Celera | 9:111645140 | TGGGTCCTGAGAGGA[C/G]AGGGATTTATAGCAT | 20840 |
rs51622381 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111629896 | GAGTGAATATATGCC[A/G]CCTTGACTTCAGTCT | 20840 |
rs51628129 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111656254 | TCCACCCTCTGTGCC[C/T]ACTGTCACTCTGTCT | 20840 |
rs51631105 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111642967 | AGACGACCTTAATGC[A/G]GACATGTTGATTCAC | 20840 |
rs51651510 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111665515 | TTGTTTTAAACCTGT[A/G]CCCTTTGGTGGCTGT | 20840 |
rs51654884 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577258 | TATGCACTAGAAGCA[C/T]AGATATGGCAAGATT | 20840 |
rs51659411 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111577447 | CCCACATGAAAGGGT[A/G]GACCATTGAAGGCAC | 20840 |
rs51671944 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Stac | GRCm38.p3 | 9:111685840 | TTTCCAGGTGGTGCT[A/G]GAATAAGCACTTGAT | 20840 |
rs51672640 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111642145 | GAGCCTCCTCTAGAC[C/T]AGGATACAGATCTTT | 20840 |
rs51693467 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111685238 | TCTCTTTTCTCATAG[A/G]TTTCTCACAGTTTTT | 20840 |
rs51693561 | snp | G/T | 0.142012 | 0.225474 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111573787 | AAGTTGGTAGACAGT[G/T]GGTATCACCCATCTC | 20840 |
rs51700241 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | GRCm38.p3 | 9:111669917 | ATCAAGTCTATAGCT[C/T]AGTGAGAAGCATAGG | 20840 |
rs51704919 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111685502 | CAGGGACGGTTAGCT[A/G]GTTAGATCTGTGATG | 20840 |
rs51705165 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Stac | GRCm38.p3 | 9:111567274 | ATGTGTTCATAATAG[A/G]TAACCCAATTCCATC | 20840 |
rs51711505 | snp | A/C | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111657626 | GGGCACACAGGCACC[A/C]TGAAACCAACAGCAA | 20840 |
rs51712498 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111673704 | GCAGCACTCTCTGAT[C/T]AAAAAGCACCAGAAG | 20840 |
rs51718023 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Stac | GRCm38.p3 | 9:111688121 | ACAATGATGGTCTCG[A/C]CAGCTCCTATCCCAA | 20840 |
rs51720418 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111675194 | AATAACATAGTGATA[C/T]GAGCAGTGATGGTGA | 20840 |
rs51720839 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111669591 | ACAGAGGCAGGATGG[A/G]CACAGCTTTGACAAG | 20840 |
rs51723847 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111639747 | ACTCCTATGCATAAC[C/T]ATTGAGGTAAGTTCT | 20840 |
rs51725343 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111658255 | AAGACTTGGGTTTTC[C/T]ATCTTTATTTGCTGC | 20840 |
rs51730419 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111621161 | ATGCTGTTGAGACAG[C/T]GCATGCAAGGGAGCC | 20840 |
rs51731547 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111583339 | TGCTTTCATTCAGAC[A/T]CACCCACAGAATGTC | 20840 |
rs51731811 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111639749 | TCCTATGCATAACCA[C/T]TGAGGTAAGTTCTAT | 20840 |
rs51738298 | snp | C/T | 0.18 | 0.24 | intron-variant, upstream-variant-2KB | Stac, Gm36034 | Mm_Celera | 9:111594104 | ACTTGAGAATCATAA[C/T]TTTGTTGCCTTTGAA | 20840 |
rs51780145 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Stac | GRCm38.p3 | 9:111658456 | CGCAAGTGGCAAAAG[C/T]CTCCAGGGAGCTGGC | 20840 |
rs51781946 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111641449 | GAGTCAAATATTCCA[A/G]CCCCAATTAGAGTCA | 20840 |
rs51783721 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111621681 | AGGACGAGAAGCTGG[C/T]AAACCCTTTTGGTGC | 20840 |
rs51787991 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111642966 | AAGACGACCTTAATG[C/T]AGACATGTTGATTCA | 20840 |
rs51798920 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111629763 | ACTTTAGTGACAAAG[C/T]TGGATATGGTGGTAT | 20840 |
rs51826949 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111685747 | GTGTATATGTTATAT[A/G]CTCAGACACTGCATA | 20840 |
rs51829470 | snp | A/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111570571 | GTGTGTGTGTGTGTG[A/T]GACTTCAGAACTGTC | 20840 |
rs51832645 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111641741 | GCTTTTAATCTGATG[G/T]TGCCTAACAGGTCTG | 20840 |
rs51833486 | snp | A/C | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111655430 | AGATGTGGGATAGTT[A/C]GTGGAAAATATCTAG | 20840 |
rs51835598 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111615697 | AGCTAGCCTTAAGTG[C/T]ATCTTCACATGAATA | 20840 |
rs51851270 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111637355 | AGGACATTTCATACA[C/T]GTATGTTATTGGTTC | 20840 |
rs51855870 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111673343 | TGAGCGGATCACCAT[C/T]TCAGGATGAGGGTTT | 20840 |
rs51861651 | snp | C/T | 0.21875 | 0.248039 | intron-variant, upstream-variant-2KB | Stac, Gm36034 | Mm_Celera | 9:111593685 | GCTGACAACTTGATC[C/T]AGGAACTCTCTCCTG | 20840 |
rs51880011 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Stac, Gm36088 | Mm_Celera | 9:111575771 | GATCACTCTGTCCTC[C/G]TGCCTGACACTGTCG | 20840 |
rs51888364 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Stac | GRCm38.p3 | 9:111623295 | GACCCGCAGTTCTGC[A/C]CCATGATTACGGCCA | 20840 |
rs51912692 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111583755 | TCTCCATCCTTTGTG[A/T]CCGAGTTCCCAAAGT | 20840 |
rs51917060 | snp | C/T | 0.124444 | 0.216185 | missense | Stac | Mm_Celera | 9:111562702 | CTGATGAAGCCGTCC[C/T]GTTCTTCCTCAGAGG | 20840 |
rs51924716 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Stac | Mm_Celera | 9:111569334 | GGCCAGATTTGCTGT[C/G]TTTCTTCCTGGCCTT | 20840 |
rs51929453 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111640066 | TAACATTTCAGGAAA[C/T]TTTATCCATATATGT | 20840 |
rs51930132 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111677359 | TGATTCACTCAATGT[C/T]CCGTCTCTTCCTCTC | 20840 |
rs51931106 | snp | G/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | Mm_Celera | 9:111571931 | TTGTTGGAATGAAAT[G/T]CGATTGGACAGCTTC | 20840 |
rs51933624 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111636361 | GTCCAGCTCCTGCTG[C/T]TCAGACTCCTGGGCC | 20840 |
rs51939761 | snp | G/T | | | intron-variant | Stac | GRCm38.p3 | 9:111641167 | AAGGTCTGAGGTGGA[G/T]AGTGAGTGGGGAGGC | 20840 |
rs51948729 | snp | A/C | 0.391111 | 0.206368 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111578278 | TATGTGCCTCATTAC[A/C]GTAGTATTTTTGTAG | 20840 |
rs51949294 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111570697 | CCCACATGTTGACTA[A/C/G]CAACTCTAGATCACA | 20840 |
rs51974134 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | GRCm38.p3 | 9:111621182 | CAAGGGAGCCGTAGC[C/T]GTGTCATTTTCTCCC | 20840 |
rs51980181 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111667336 | GAAATGAATTTTAGC[A/G]TAGACTCCAATCAGC | 20840 |
rs51997583 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111584323 | ATAAAGTTTGAGATC[A/C]CAAGACAAGGGAGGA | 20840 |
rs52002580 | snp | G/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111572922 | TTATTATCTTTATTT[G/T]GGATGGTTTGATTGG | 20840 |
rs52013259 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111643268 | AAGCAAATATCTCAT[C/T]CTGAATTTTCCTACG | 20840 |
rs52022416 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111659637 | ATGTCCCGATGACCT[C/T]GGCATGAATAAATCA | 20840 |
rs52066008 | snp | C/G | | | intron-variant | Stac | GRCm38.p3 | 9:111636799 | TAGCACAAAAAGTGT[C/G]TTCTTCTCACCTCCC | 20840 |
rs52105698 | snp | A/T | | | upstream-variant-2KB | Stac | Mm_Celera | 9:111691823 | GACAGGCAGACAGAC[A/T]GATAGATAGATACTA | 20840 |
rs52110391 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111672708 | TATCTTGGCCATTTT[A/T]TCTTATCGAATATGT | 20840 |
rs52114363 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111646413 | GCATGCATGCACATG[C/T]ACTCACCCACACATG | 20840 |
rs52121046 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111670894 | CATACATACTTGCAT[A/G]AATGCCTACATGAAA | 20840 |
rs52121368 | snp | C/G | | | intron-variant | Stac | Mm_Celera | 9:111629985 | GCATGCACAGACACA[C/G]ACACACACAGACACA | 20840 |
rs52124537 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111629968 | TGTGCGCATATCCAC[A/G]TGCATGCACAGACAC | 20840 |
rs52126935 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111624541 | TTTGAAACACAGGAG[G/T]TCATTACATGGAAAG | 20840 |
rs52150225 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | Mm_Celera | 9:111657773 | GGATGGGCAGGGATC[A/G]CTTCTCTATCAAAGA | 20840 |
rs52161959 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Stac | Mm_Celera | 9:111635617 | CTTGTACCTGAAACA[C/T]GTGGAAAGAAGCATG | 20840 |
rs52163927 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111637651 | ACgtgtgtatgtatg[C/T]atatatgtatgtatg | 20840 |
rs52164584 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111648315 | CCCAGGCCTCTGCTA[C/T]CCCTGCCCAAGCCTC | 20840 |
rs52166967 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Stac | GRCm38.p3 | 9:111653327 | TGTTACGATTTTTTT[A/T]AAAAAGTGCCTCTTT | 20840 |
rs52195968 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111669669 | AACTTCTTGTGACAT[A/G]GCTCTGAGCAGGTCA | 20840 |
rs52210539 | snp | A/C | | | intron-variant | Stac | GRCm38.p3 | 9:111610501 | TGAGTTCCAGGACAG[A/C]TAGGGCTACACAGAG | 20840 |
rs52226116 | snp | C/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Stac, Gm36088 | GRCm38.p3 | 9:111579300 | GGTGAACGCAGCTCT[C/T]TCCACAGGTTAAAAC | 20840 |
rs52226288 | snp | C/T | | | intron-variant, upstream-variant-2KB | Stac, Gm36088 | GRCm38.p3 | 9:111572201 | CTTCTTTTGTCCCTG[C/T]TTGTGGTGTGTGTGT | 20840 |
rs52230611 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111610232 | GAAACAAGGATGTCA[C/T]TGGATTTCAAGTAAG | 20840 |
rs52236223 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111686398 | AGCCACCTCCCTAGC[C/T]CTTTTCCTCCCTCCC | 20840 |
rs52248619 | snp | C/G | | | intron-variant | Stac | Mm_Celera | 9:111629979 | CCACATGCATGCACA[C/G]ACACAGACACACACA | 20840 |
rs52253294 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111629972 | CGCATATCCACATGC[A/G]TGCACAGACACAGAC | 20840 |
rs52274745 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111631948 | GCTGGGTGATCTCAG[A/C]ACCTTATAAAACCAG | 20840 |
rs52275325 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111622226 | GTGTGTGTGTTCCTC[C/T]CTCCTCGGTTTTTGA | 20840 |
rs52276997 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111567802 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 20840 |
rs52284637 | snp | C/T | | | upstream-variant-2KB | Stac | GRCm38.p3 | 9:111691951 | ATTAGCCAACTGACA[C/T]GAGGGACAATACAGG | 20840 |
rs52294518 | snp | G/T | | | intron-variant | Stac | Mm_Celera | 9:111672207 | ATCTGGAGCACCCAT[G/T]CACAAAGCAGAACTC | 20840 |
rs52295984 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111686990 | GTTACCAGCACCAGA[C/T]CTCTCAGGGAGGTTC | 20840 |
rs52315579 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111567814 | CTTTCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 20840 |
rs52318726 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Stac | Mm_Celera | 9:111632534 | ATACATGAAAACTCT[G/T]TCTTCAAAAGCTTTT | 20840 |
rs52321447 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111632143 | GTGCCGCAGTGCAGG[A/G]GAACACCAGGGCCAA | 20840 |
rs52324777 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111679553 | GCAATAATGAGACTC[A/G]GTGCTCTCTTCCCCA | 20840 |
rs52327167 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111629960 | TGTGTGAATGTGCGC[A/G]TATCCACATGCATGC | 20840 |
rs52348752 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111672577 | TTGTATTCATGGTCA[A/G]ATATTATTGAAGCAT | 20840 |
rs52355125 | snp | G/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111672589 | TCAAATATTATTGAA[G/T]CATGCTGCAGTTTTC | 20840 |
rs52370796 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111648314 | GCCCAGGCCTCTGCT[A/G]TCCCTGCCCAAGCCT | 20840 |
rs52378370 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111567794 | CTTTCTTCCTTCCTT[C/T]CTTCCTTTCTTCCTT | 20840 |
rs52389678 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111646451 | TAAAAATAATGCACA[C/T]AGACACAGGAAGAAA | 20840 |
rs52391189 | snp | C/G | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111643690 | AACGTGCCATTTCAT[C/G]CTGAGATTTTAATTC | 20840 |
rs52412936 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Stac | Mm_Celera | 9:111635846 | TGTGGTGTGTGTTTA[A/G]GACTTAGTATTTCAA | 20840 |
rs52438336 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111581490 | TGCAATTATCACTGT[C/T]CATAGAAATTAAAGA | 20840 |
rs52438361 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stac, Gm36088 | GRCm38.p3 | 9:111574327 | TCTTGTGTCTGATGT[A/G]TTAGTGCATGATGTA | 20840 |