SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3022801 | snp | A/G | 0.33099 | 0.236518 | intron-variant | Satb2 | Mm_Celera | 1:56835144 | GCCATTTGGACACTG[A/G]CTCCTTTTTGTTAAT | 212712 |
rs3089908 | snp | A/G | 0.287335 | 0.247197 | intron-variant | Satb2 | Mm_Celera | 1:56835113 | CATCTTTTTGTTTAC[A/G]CCATCTCTCCAGGAG | 212712 |
rs3653534 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Satb2 | GRCm38.p3 | 1:56809453 | CTCTTAGCACATACA[A/G]CTGTAGGAAGGGGAT | 212712 |
rs3664259 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Satb2 | Mm_Celera | 1:56814006 | ATACCAAACACTTCA[C/T]AGGACAAGGCACACA | 212712 |
rs6152247 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Satb2 | Mm_Celera | 1:56888858 | GCAAGAAGCCTCTAT[C/T]AAATGAAAAGAACCA | 212712 |
rs6152302 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Satb2 | Mm_Celera | 1:56888888 | AGCTAGGCTCAACAC[A/T]TCTGTTTNCTGAGGG | 212712 |
rs6152314 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56888896 | TCAACACNTCTGTTT[C/T]CTGAGGGTAGAAAGT | 212712 |
rs6154767 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56876148 | GTTTNTGCCTATTTA[C/T]TTCATGTTTGTCTTA | 212712 |
rs6154863 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56882762 | ctctctctctctctt[C/T]ctctctctctctctc | 212712 |
rs6155380 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Satb2 | Mm_Celera | 1:56882840 | ctctctctcCTTACA[A/T]CTAATGATGCCCACA | 212712 |
rs6155498 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Satb2 | Mm_Celera | 1:56882901 | AAAGTAAATTCAGCA[C/T]ATGATGAAAAAAAAT | 212712 |
rs6155864 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Satb2 | Mm_Celera | 1:56876315 | AAAACACTCAGGAGC[C/T]ANTGAAACACAAATG | 212712 |
rs6155865 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56876317 | AACACTCAGGAGCNA[C/T]TGAAACACAAATGCT | 212712 |
rs6156443 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Satb2 | Mm_Celera | 1:56876433 | GGGTAAAGTGGCTGC[A/G]AAGTCCCAGGCATGA | 212712 |
rs6156494 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Satb2 | Mm_Celera | 1:56876462 | GATCAGACTTAAGGC[C/T]TTTGTGTCTCCTTCC | 212712 |
rs6156557 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56876504 | TCCTCACTCCCACAG[G/T]CCCCAGGAAAGCATG | 212712 |
rs6157102 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56876602 | GAGAAGAACTGCAGA[G/T]CAGGGGCCAGTNCAA | 212712 |
rs6157480 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56876614 | AGANCAGGGGCCAGT[A/G]CAAGAGAACATCGTT | 212712 |
rs6157538 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Satb2 | Mm_Celera | 1:56876650 | GTGTTACAGCCCGTG[C/T]CTGCAGAAGCCTTAC | 212712 |
rs6164778 | snp | A/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56928700 | TTGCCAAAGCCACTG[A/T]CCTCAGTCTGGCCTT | 212712 |
rs6164900 | snp | A/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56928771 | ATTAGCCACAGATGA[A/T]TAATAACCGATTCCC | 212712 |
rs6236725 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56964701 | GCGTGGGTGGGTGAG[C/T]Gcacatacacacaca | 212712 |
rs6237814 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56964903 | TCTGTTTAATGTGTA[C/T]GTTCCATTGCATATA | 212712 |
rs6238252 | snp | A/C | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56926440 | TGTCCTGTTTACTGT[A/C]TTTCAAACAATGTTT | 212712 |
rs6238391 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56965030 | AGGACATGTTAGACG[A/G]GTAGATGACCCCCAA | 212712 |
rs6238718 | snp | C/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926505 | tgtgtgtgtgtgtgt[C/G]tgtgtgtgtgCGCGC | 212712 |
rs6238815 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926561 | ATGTGCACATGGGTA[C/T]AGGTACCTATGGAGG | 212712 |
rs6238902 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56965125 | GGATGGGTAGGGAAG[C/T]CTTCCCTCTGCAACC | 212712 |
rs6239296 | snp | A/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926629 | ACCCAAATTTGGACT[A/T]CGANTACCTNCCAGG | 212712 |
rs6239309 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926633 | AAATTTGGACTNCGA[A/G]TACCTNCCAGGTGTT | 212712 |
rs6239311 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926639 | GGACTNCGANTACCT[G/T]CCAGGTGTTAATAAC | 212712 |
rs6239337 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56965160 | GTCCTTCCTATCAGC[A/G]TATGCTCCAACTGCC | 212712 |
rs6326859 | snp | A/T | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56904525 | ATCAAAAGGTTTGTA[A/T]NCAGTGCTAAGCATC | 212712 |
rs6326861 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56904526 | TCAAAAGGTTTGTAN[G/T]CAGTGCTAAGCATCC | 212712 |
rs6336903 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56917322 | TTAAAATATAATACA[C/T]AGGCCAGGCACACAT | 212712 |
rs6337424 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56917367 | AGTCCTGGTCCAGTG[A/G]CTCAATTTTGTTACA | 212712 |
rs6337500 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56917400 | ATAATACATATGCTT[A/G]TTTTGAACATAAAAA | 212712 |
rs6338592 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56917576 | AGACTGAATGTCTAC[G/T]AACCAACAAGCNAAG | 212712 |
rs6338623 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56917588 | TACNAACCAACAAGC[A/G]AAGGTATAATTAAAA | 212712 |
rs6341554 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Satb2 | Mm_Celera | 1:56904968 | AAAATGAGACATTAG[C/T]TTTAATATCCAAAGG | 212712 |
rs6374058 | snp | A/C | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56958086 | TTGGCTTATAAGCAT[A/C]GGTGCAGGCTTGTGG | 212712 |
rs6375223 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56958319 | GGGGGCTTTCCTAAG[C/T]GGTGCTATCAGAGAA | 212712 |
rs6375686 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Satb2 | Mm_Celera | 1:56958381 | ATGGAAAGGAATTGT[C/G]TCTCTCAACCTTGCT | 212712 |
rs6403535 | snp | A/C | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926881 | TAAGTGTGCACGACG[A/C]ATGATAACTCACAGG | 212712 |
rs6404090 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56926992 | AGAAAGCCACCCATC[C/T]GCCTGTCAGCGGGCA | 212712 |
rs6404717 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56927130 | ATAGAGGAAGCAGCC[A/G]AACCATTTATCCNGA | 212712 |
rs6404740 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56927143 | CCNAACCATTTATCC[A/G]GAAAAGACTGTTTTA | 212712 |
rs6411272 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Satb2 | Mm_Celera | 1:56888425 | TGTAACAGAATCACA[G/T]AGCTTATGTTTAGGA | 212712 |
rs6411341 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56953810 | CTCGCACTATCTGTC[A/G]CCTAAGATTCCAGAA | 212712 |
rs6411834 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Satb2 | Mm_Celera | 1:56888532 | ACATATTTAAGGATG[A/G]AGCCTGCATTTTGTT | 212712 |
rs6411879 | snp | A/C | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56888552 | TGCATTTTGTTTAGG[A/C]CATCGGTAAGCTGGC | 212712 |
rs6412419 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Satb2 | Mm_Celera | 1:56888622 | TGTATGCTGGTGACT[C/G]CATGACTTGACCAGG | 212712 |
rs6413099 | snp | A/G | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56888769 | CATGGTCACCAGCAA[A/G]TGTTAGAAAGCAAAC | 212712 |
rs32742539 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56901669 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 212712 |
rs32778009 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Satb2 | Mm_Celera | 1:56799388 | TAACCGCATTTAGAT[A/G]GGCATTTTAATATCC | 212712 |
rs36242908 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Satb2 | GRCm38.p3 | 1:56955876 | GGAAAGAGACAGACA[C/T]GTGGATTCACGAGCT | 212712 |
rs36246795 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56836405 | GGGATCACACTGTCC[A/T]TGGGAGAACTGCTAA | 212712 |
rs36252917 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56934019 | ACCTCAAGATGTCCA[G/T]GCAGAGGCAGCACCG | 212712 |
rs36254185 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56869719 | TCTTTAAGCTCCACC[C/T]TGCTGTGTTGCTGAA | 212712 |
rs36254371 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56836241 | AAATCAAAACCAAGA[G/T]AAGCTTGATGCAATA | 212712 |
rs36260345 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56939895 | CTTAGAGCTGGAAAA[C/T]GATGGCGTCCAAACA | 212712 |
rs36260772 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56881437 | GGCACATAAATGCTT[A/G]GAATACCAGCCTATG | 212712 |
rs36264461 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Satb2 | GRCm38.p3 | 1:56915862 | CTCAGTCCATGGCAC[C/T]TGCTAAGAGTTGCTG | 212712 |
rs36266348 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56903908 | GTTATCTGCAAACAT[C/T]CAGAAAATGCCTGGT | 212712 |
rs36266711 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56812000 | ACTGTGTGTCTGAGG[C/G]CTGTGTAGGATATGG | 212712 |
rs36269229 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56854261 | TGCCTCATTGTAGGG[A/T]ACAGAACATTTTCCA | 212712 |
rs36269637 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56828772 | CTCTTAAGTCCAATG[C/G]CCTGGCATGTGCTCA | 212712 |
rs36269733 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56933264 | GGAGTTAACAAGTCA[C/T]GTGGTGCGATTCTTA | 212712 |
rs36269740 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56876179 | AACTGACTGAACACC[A/G]CTGTTTCGCCTATAA | 212712 |
rs36273503 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56812589 | AACGAGCTGTCAGTC[C/T]AGGAGCATTCTTTTT | 212712 |
rs36273696 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Satb2 | Mm_Celera | 1:56882628 | CCATGGAAAAAGTGA[C/T]CACTGTTCACTTAAC | 212712 |
rs36273806 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56801234 | ATAGATAAATATAAA[C/T]GTAATCCTACAATTC | 212712 |
rs36274161 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Satb2 | GRCm38.p3 | 1:56909793 | CATGTGCGTGCACCC[A/G]TAAATAGATGCAGAA | 212712 |
rs36276263 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56830212 | GTAAGCACTGTGGTT[C/T]AGCCTCCCTGAATAA | 212712 |
rs36279138 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56915805 | GGAAAGCCTTTGGCT[A/G]TAACCCTAAGAGCAA | 212712 |
rs36280067 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56814460 | GGAATCTTGAACCAA[A/G]AAAGAATCTACAAAA | 212712 |
rs36280661 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56900164 | GACTCCATAGCTGTG[A/G]GGCAAAATTCAGAGG | 212712 |
rs36280769 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56943515 | GACTCTACATCTGCT[A/G]AGGTTCATCCCTGTT | 212712 |
rs36283732 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56894664 | CTATATATTAATATG[C/T]AATGCCTGACAATCA | 212712 |
rs36286174 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56959773 | AGAGAAGGTGGTTGC[A/G]TGAAAGAAATACCAC | 212712 |
rs36288113 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56818685 | ATAGATGAAGCAAAC[C/T]AAGGTGTGAGTGTAT | 212712 |
rs36288364 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56802546 | TTATAAACTACTTCA[A/G]TCAGCCTTGGTTTTC | 212712 |
rs36291231 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56854513 | ATGAGCTTTGCAGAC[C/T]ATTGCTAGGACCAGC | 212712 |
rs36294685 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56837403 | TATGTTAGGTGTAGA[G/T]GTGTCTGATGTACCT | 212712 |
rs36295390 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56949827 | TGAGACGACTCAAAC[A/G]TTAGGCAAAGGAGAT | 212712 |
rs36295725 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56803971 | TAAGGTGCAGCACCA[A/T]GTTCCTGTGATTTTC | 212712 |
rs36300180 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56905713 | CCTCTCAACTCACCA[A/G]TCTGGGAGCCTAGAA | 212712 |
rs36302941 | snp | A/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56886382 | GATCCAATATTTATC[A/T]AAAATTCAAAGGGCT | 212712 |
rs36303111 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56880994 | TTCCAGGCTCCTGGT[A/G]CCTATGGTCTGTTGC | 212712 |
rs36305174 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Satb2 | GRCm38.p3 | 1:56837072 | AGGAAGGAGACCGCT[A/G]GAGGAGGTGACAGTT | 212712 |
rs36309515 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56939783 | CTGTGGGCTTTCAAC[A/G]CGACAATCATTTTCC | 212712 |
rs36311999 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56910492 | CCCTCTCAAATTATC[C/T]CAGAGACCCTCTGCA | 212712 |
rs36313415 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Satb2 | GRCm38.p3 | 1:56842965 | TTATCCCAGCAGCCT[C/T]GACTCTTCACTTCCC | 212712 |
rs36314309 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56945990 | AGAGTATTTAACCTT[C/T]TAATCATCAGAATGG | 212712 |
rs36314601 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56956101 | GGACCACGGCCTACA[C/T]TGCAGCAAAACGCCT | 212712 |
rs36316567 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56886022 | TTTATTTCTTTTACT[C/T]CATCAATTCTGTTAT | 212712 |
rs36322383 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56934419 | ATATGTGAGACGTTA[C/T]AGCAGCTTTTATTGG | 212712 |
rs36327710 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56955555 | ATAACAAAGAATGAG[C/T]GACACCAGGGACCGC | 212712 |
rs36328370 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56811296 | TGCACACCACTATCA[C/T]TGTTATCATGTCTTC | 212712 |
rs36330619 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56816252 | GGCCCGCCAAAATTC[A/G]CACCACTGGATAGCA | 212712 |
rs36331495 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56953333 | GCGTCTGAAAGGACC[A/G]GAAAATGATGCAGCT | 212712 |
rs36333172 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56935938 | TACATATTTATGATA[C/G]AATGCTTGTTTAACA | 212712 |
rs36333504 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Satb2 | Mm_Celera | 1:56825973 | AAGGCTGAGAACCAC[G/T]GGTCCAGTGCCTCAG | 212712 |
rs36346726 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56889426 | TTCTTTTTACTCACA[A/G]CAGCAGGTAAATGTG | 212712 |
rs36357831 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56830671 | GAGGTCTTACACGAG[C/T]CCCTTTGTTGCAGTC | 212712 |
rs36361133 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56821277 | TGGGAAAGCCTTTCT[C/T]TGCAGACTGTCCTGT | 212712 |
rs36363965 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56903051 | GCTTATGGTGGAGGA[A/T]GATCCACTTTCTTGC | 212712 |
rs36365041 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56817676 | ATACATACCATGGTG[C/T]TTGACAAAATTTATT | 212712 |
rs36373218 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56838975 | TCTATAGAACACTAA[C/T]AAGGCCTAGCTTGAG | 212712 |
rs36373761 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56890344 | TATTGTAGTAGTAGT[A/T]TATCTTAACTACTAG | 212712 |
rs36377325 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56869079 | GGTCTCTCTTGGCAG[C/T]CTCCTAACTGGAAGT | 212712 |
rs36377407 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56882469 | TCATATGACTGGGTT[C/G]CTTAGGTGGATTTTT | 212712 |
rs36378250 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56853184 | TACCATATCTAAAAA[C/T]TATGCAGGTTCCCAA | 212712 |
rs36379699 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56861738 | TATATTCCAAACACA[A/G]TGTAAATAAAGCTTA | 212712 |
rs36385110 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56878528 | GTCTTCTGTTTCCCG[A/C]AAGATTACCTAAAGA | 212712 |
rs36391342 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56949870 | TGCTTTATAGTGCTG[C/T]TTTCCTTGGTTACCA | 212712 |
rs36396115 | snp | A/G | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56965375 | CACCTGACCTGATCC[A/G]CATTTCTTTGGCTCT | 212712 |
rs36403136 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56887409 | TTACCTCTCCTATGC[A/G]CCCTGTGAGTGTGTG | 212712 |
rs36406489 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56894133 | GAGACACAGAGAATG[C/T]GCACGTACCACGCAA | 212712 |
rs36407319 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56797287 | GTGTGACTGGGATTA[C/T]ATTTGCAAGGCCACC | 212712 |
rs36407441 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56896938 | AACTCTCAAGGACTG[A/G]AGTTTTGTAGTCAAA | 212712 |
rs36408066 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56877645 | TGATGTCATATAATC[A/T]GTGCTTGAATTTGCT | 212712 |
rs36408396 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56942253 | AAGCAAGCTCACACG[G/T]TAGGGCATACACATT | 212712 |
rs36410605 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56827470 | TTGATACAGACAACC[A/G]TACACTATTGTGAAT | 212712 |
rs36412349 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56968414 | TCTCATTAAAAGTAT[A/G]TTTTCACATCTCTAA | 212712 |
rs36412556 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56951164 | TTATGGCTTTATAAT[A/G]CAATTCTGTTTTTAC | 212712 |
rs36417763 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56837425 | GATGTACCTTCATCA[A/G]TAGGGCTGGCTGGCC | 212712 |
rs36419730 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56945860 | AGCCTTTCAGAGGAA[C/T]GGATAACCCTGTTTC | 212712 |
rs36422348 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56958538 | ACACAAACCTACAAC[A/G]GGCCCATTATGGGGC | 212712 |
rs36432743 | snp | A/C | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56960184 | TTTCAAGTAATGGCA[A/C]CAAGAAAATGTTTTA | 212712 |
rs36438042 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56837539 | TTCCAAAAGCAGCCA[C/T]GACAAGGTCTATTTG | 212712 |
rs36441995 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56807096 | ATCCCACAGCCTCTC[A/G]ACTTTATTTCTAGTT | 212712 |
rs36443995 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56957153 | AGTGGGCATCTGATA[G/T]CTCCCTCCAGGGACA | 212712 |
rs36447527 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56815407 | TTCCTGGTTATTATA[A/C]TTCATGGGCTAAGTA | 212712 |
rs36457098 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56850644 | AGCGAGCAAGGTAGG[C/T]GCTCAGGAGGAAATA | 212712 |
rs36467878 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56857060 | TTTAGTTCTGATGTC[C/T]ATGCTCAGTTAACAA | 212712 |
rs36468023 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56896403 | CCGTGTCTACTCTTT[A/G]CTCACTTTCAGAACA | 212712 |
rs36472795 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56954423 | CCCCGTCCTCAGGGG[A/C]TGATGTGGAAATTTT | 212712 |
rs36473414 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56866647 | AATTTGATAAGGACA[A/T]CTCCCAACCAATAGA | 212712 |
rs36475193 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56826382 | TGATCTTCTCTGTGC[C/T]ATCTACTCTTGAACC | 212712 |
rs36475619 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Satb2 | GRCm38.p3 | 1:56865698 | AAAATGTGTTCTGTG[A/C]GTCAATTAGACCTTT | 212712 |
rs36475674 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56828141 | GGATCCCCATGGAAA[C/T]GGTGTAGCTTCAGCT | 212712 |
rs36476851 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Satb2 | Mm_Celera | 1:56936099 | GAGCCACCCGCAGAG[C/T]CATAGACAAAGAAAC | 212712 |
rs36481749 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56956158 | GCTCAAGCCCATGGC[A/G]TATTGCTGGAAGATA | 212712 |
rs36483452 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB | Satb2 | Mm_Celera | 1:56979776 | GCCTCTGCCCAGTAA[C/T]GTCCAGAGTTCAGAG | 212712 |
rs36492107 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56852847 | TTTCTCTCATAATGA[A/G]CCATGCATAGAAAGA | 212712 |
rs36492665 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56965237 | CCCTGGGTTGACAAT[G/T]ATATTTCTAAGTATT | 212712 |
rs36499232 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56852545 | CTGCTGAAATGATTA[A/G]AGGAAAATCCAGATC | 212712 |
rs36503500 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56877323 | GACCACTTTCCTGTG[C/T]TGGAACTTTTCATAT | 212712 |
rs36504542 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56919456 | GGGAACAGAATCCAG[C/T]GAGGTTCTTCGGGCA | 212712 |
rs36504930 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Satb2 | GRCm38.p3 | 1:56900887 | TGGCACAGAGGAGAA[C/T]CCAGGAGTCATTTTG | 212712 |
rs36505620 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Satb2 | Mm_Celera | 1:56795048 | GCGGGACTGCTGAGT[C/G]GCCATCTCAAGCCTG | 212712 |
rs36506801 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Satb2 | Mm_Celera | 1:56795570 | TCTCTAACCTAACAT[C/T]ACATTAAACTATGTT | 212712 |
rs36507195 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56836179 | AATGCATAACCTCAG[A/C]CAAATGATGAAAAAA | 212712 |
rs36508962 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56908567 | ATAGGTGCTCATTCC[A/G]CAGACAAATGTTTCT | 212712 |
rs36509664 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56800506 | GGCAATGTTCTTAGC[A/G]TTTTTTGTTACCACT | 212712 |
rs36510371 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56805868 | GATACAAACAAATTA[A/C]AAGTTCAAAGCCTGA | 212712 |
rs36512771 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56890179 | TTTTATGTTAACATG[C/T]TTGCAAAGATAAAAC | 212712 |
rs36513788 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56961040 | CAGGGAAGGACAGCC[A/G]ATGCAGATCACAGCT | 212712 |
rs36519729 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56937953 | ACCATTCAAGTTCTG[A/G]GCTCACTGAAAGACC | 212712 |
rs36519832 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56891503 | GCCAGTCCTAGAGTA[A/C]TGTCAAAGACAGAGA | 212712 |
rs36532553 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56955445 | TCAGGGCTGCTTAAC[C/T]GCTAGGAAATTCAGT | 212712 |
rs36533191 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56877577 | CCTAAGCTTGAGAAC[C/T]AATATGCTATGTCAT | 212712 |
rs36535847 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56952330 | CTTCAATACTTTTCA[G/T]TAAGCAATGTTCAGG | 212712 |
rs36536483 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Satb2 | Mm_Celera | 1:56865942 | ATCACTTTAAAAATC[G/T]AAAGTACTACAACCA | 212712 |
rs36540310 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56857311 | TAATGAAGCTGCCCC[C/T]TACCTCGTTTCTCTC | 212712 |
rs36543814 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56879967 | CAATATTGTAGATAA[C/T]GACCTTGTTAAAAAT | 212712 |
rs36545171 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56862501 | CAGACGGAAGGTCTC[A/G]GAGGGGACGTGATGT | 212712 |
rs36548935 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56839606 | AAATGTCAGCATATG[C/T]AACCAAAAGGGAATG | 212712 |
rs36551401 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56935303 | AAAGGGTTATTTGCC[A/G]AGGTTTAAAGCAAGT | 212712 |
rs36553782 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56894082 | CCAGCACATGCACTT[A/C]TGCTTCTATGGAAAC | 212712 |
rs36556016 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56887210 | ATTTTGTAATAGCCA[C/T]CAGTATTTGTATGAA | 212712 |
rs36557232 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56901768 | GGAAGTATTAGATTG[A/C]AGACAGCTATCTCCA | 212712 |
rs36561867 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56965973 | TGAAAGTTCCTCTTG[A/C]AGCCAAACACTAAAA | 212712 |
rs36563890 | snp | C/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56942158 | GCACTGAACTGTAGT[C/G]TCACACTGTACTGTG | 212712 |
rs36565694 | snp | C/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56962176 | ATCAGACCAACAGTC[C/G]CGCAAGTGCCTGCTG | 212712 |
rs36567330 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56950642 | TTGTGATTGGAGGGA[A/G]CAACTGCTGGCTAGC | 212712 |
rs36567705 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56904691 | TCCAGATAAGCCAGG[A/T]TGATAACTTTCACCC | 212712 |
rs36570053 | snp | A/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56823109 | TTGGAAATTCATGCC[A/T]CGAAAATCTGCCTTC | 212712 |
rs36575266 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56862113 | CAGAGAGACCTCTGC[C/T]AAACGGCATGGATTG | 212712 |
rs36578502 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56817421 | CAGATACAATGACAG[C/T]GCCTCTAGTTCTGGT | 212712 |
rs36580544 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56889453 | TGTGATCAGTAAACA[A/G]CCTTGAAGCTGCATG | 212712 |
rs36580948 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56880503 | CAAGCCTGCCATGTA[C/T]ATCACAGCTGAGGTG | 212712 |
rs36583620 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56836297 | CACAGCCATAAAAGA[C/T]GGAGGAAGAATCGCA | 212712 |
rs36583629 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Satb2 | Mm_Celera | 1:56951120 | TTGGAAAAATTAATC[A/T]TTTTACTAGTACTTG | 212712 |
rs36584445 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56852801 | CACTTTCCAAGGTCA[A/G]TAAGACAGTAAGATT | 212712 |
rs36589548 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56804503 | GCAGAGTGTACAGAG[A/G]TAAGCTGAGTTGATC | 212712 |
rs36599825 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56857371 | CTTACGGATAGAACA[G/T]CTTTTCCATGACCTA | 212712 |
rs36602140 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56823734 | ATGAACACAGCAGTT[A/G]CCTAAAAAGAACTGG | 212712 |
rs36604000 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56944777 | AAAAGGTTCAAAGAG[A/G]AAGAATAAAAAGAAT | 212712 |
rs36609045 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56814474 | AGAAAGAATCTACAA[A/C]AGCAGCCCACGTTTT | 212712 |
rs36610116 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Satb2 | GRCm38.p3 | 1:56944759 | ACCTCACAGGGCAAC[A/G]TCAAAAGGTTCAAAG | 212712 |
rs36611699 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56963290 | CTGTTTCTAATGCTC[A/T]GACAGTTTCAAAACC | 212712 |
rs36613460 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56833158 | TTGCAAAAGGGTAGA[A/T]TTTTTTTTCTTCTTA | 212712 |
rs36614073 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56830688 | CCTTTGTTGCAGTCA[A/G]AATTTCTGTTACTGG | 212712 |
rs36617414 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56799030 | TTCAGTAAGGGGCCA[C/T]AGCCATTGCTCAGTG | 212712 |
rs36618782 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56822805 | ACCATTATGCAAAAA[A/G]CAGGCAATATGAATC | 212712 |
rs36618996 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56827445 | GCTCACTGTCTCTTT[A/G]TATGCTGAATTGATA | 212712 |
rs36620399 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56964821 | TCTGCTGATGGAACA[C/T]GAAACTTCCAAGATT | 212712 |
rs36621902 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56804447 | TTGTAAATAACAGAG[C/T]TTGCATTCTTCATCT | 212712 |
rs36622744 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56961607 | TTTGGTCAGTTCTCT[A/G]CAGTTGTGTGGTTCT | 212712 |
rs36634411 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56887385 | GAGTGCCTCACTCGG[C/T]CCATTTCCTTACCTC | 212712 |
rs36642770 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56939928 | GACTGAGCCCTGTAT[C/G]GATGGACAGTCTTAT | 212712 |
rs36650271 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56935047 | TTCCTTGAGGAAGCC[A/G]AGCTCACACTTGGGT | 212712 |
rs36650635 | snp | G/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56806933 | GAGTCTAAAGATTCA[G/T]CAGGGGAAACACCTA | 212712 |
rs36655305 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56862039 | TCAAATGAGACCTCA[C/T]TGAATTTTCAGGGTC | 212712 |
rs36655563 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56953433 | CACAGGGACCCAACA[A/G]CTTGCCCTATTAGCT | 212712 |
rs36658217 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56967096 | ACAATGCAATAGCCC[A/G]AAGATGAAAACAAAT | 212712 |
rs36663532 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56821907 | AGGAGATACCACCCT[A/G/T]TTGGAACAGGACTTG | 212712 |
rs36664609 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56942532 | TTTTAAAGAGTAACC[A/G]CTGAACTAAGCACCA | 212712 |
rs36666855 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56902892 | CCTCAATAACTCTGG[A/G]GTAAGCGGCAGTATA | 212712 |
rs36669083 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56955361 | GCCGAAAGAAGGACC[A/G]GTTGTAGCATTACAT | 212712 |
rs36673161 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56937933 | GAGTGCTGGGCCTGG[C/G]TGCTACCATTCAAGT | 212712 |
rs36673772 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Satb2 | Mm_Celera | 1:56878348 | ATACTCATTCTTATC[A/G]TAAGAAAACTTTTAT | 212712 |
rs36674038 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Satb2 | Mm_Celera | 1:56793711 | TAAATGATTCTCCAG[A/G]TCCTCCATGACAGCA | 212712 |
rs36674462 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56961568 | AAAAATATCAAAATA[C/T]GGTTTCTTATTTTAC | 212712 |
rs36677519 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56830620 | ACACGTGTTCCGCCC[C/T]AGCTTTACTCTTCTA | 212712 |
rs36677594 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Satb2 | GRCm38.p3 | 1:56915177 | GAAGCTGGTTCTGCA[C/T]CTGGGAGAGGTCTGT | 212712 |
rs36679192 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56941299 | GCTCATTTGTTCAAA[C/T]TTTGCTCCAAGATCT | 212712 |
rs36680037 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56891018 | TAAATTAAGGGTTGA[A/T]TTTTACGATAAAAAT | 212712 |
rs36682645 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56940226 | CTGGAGAGTATGCAA[C/T]AGGAAGTGAATAATA | 212712 |
rs36691444 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56856258 | TGTTTGTCTAAGAAT[C/T]AAAGTAGCTGGAGAC | 212712 |
rs36695738 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56836660 | AGACTGCATCTTTAC[A/G]GTGGGACCCAGTGAG | 212712 |
rs36697446 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56877178 | TATTGAAATTTTACA[C/T]GAAATCTTTCCAGAT | 212712 |
rs36697506 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Satb2 | GRCm38.p3 | 1:56916217 | TGAAACCTCCCTAGA[A/G]GACTATATCTATAAA | 212712 |
rs36699918 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56882037 | GAATATTCCCACCTA[C/T]GAAGTATTTCTGATT | 212712 |
rs36700969 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Satb2 | GRCm38.p3 | 1:56804434 | GAGGGACCCCAGCTT[G/T]TAAATAACAGAGCTT | 212712 |
rs36703863 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56884806 | ACGGTCCCCAAAATT[A/C]TGTCATCACCAGTGT | 212712 |
rs36704322 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56902056 | CTCTCTTCAATGTGC[C/T]GTCCCTTCAAGCAGG | 212712 |
rs36709038 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56964660 | ACAGATGCTTAAGGG[A/G]CTTCTTTGTAGTTTT | 212712 |
rs36709748 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56811401 | GACAATGATAAGGTG[C/T]TGCAAAGATTTCATA | 212712 |
rs36710230 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56860498 | CACAACAGTAGATGC[C/T]CGCACCAGAAATCCA | 212712 |
rs36711976 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Satb2 | Mm_Celera | 1:56795843 | ATTCCATAGGTCCAA[C/T]GTCAAAACGTCACTC | 212712 |
rs36715693 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56951482 | CAAAAATAAATGTAA[C/G]AGTGGCAAGAATAAA | 212712 |
rs36720022 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56822003 | AGTTCAGTAGTTGTC[A/G]GGTGAAGAGATAAAA | 212712 |
rs36729916 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56835672 | TTAGAGATTAGCTGA[A/G]TATTCAGGCAGTCCA | 212712 |
rs36732620 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Satb2 | Mm_Celera | 1:56912537 | AGAGCAAACTATCAT[C/T]AAGCTGCCCACCCAT | 212712 |
rs36734617 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56854455 | AGGTTTGGGCAAAGA[C/G]AGCCTCAAGGGGGCT | 212712 |
rs36741226 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56943259 | GCTGTGGTTAAAAAA[A/T]AAATAAACTGTATAG | 212712 |
rs36743231 | snp | C/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56889733 | CTTAACTTCTGGATA[C/G]CTCAAGATTTTTACT | 212712 |
rs36745583 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Satb2 | GRCm38.p3 | 1:56856364 | TGTTTATGTATTATT[A/C]CAACAGACAGGGGTA | 212712 |
rs36748248 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56917990 | CTGAGCTATTTGGCA[C/T]GCATTCGAAAAAAAT | 212712 |
rs36748845 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56963232 | GAAATGGCAATCACT[C/T]ATCCATAAGCAGCAG | 212712 |
rs36749820 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Satb2 | GRCm38.p3 | 1:56917236 | ATATCTGAAGTACTG[A/G]AAACAAAAATAAGAC | 212712 |
rs36750551 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56952003 | GGGAAGATAGTTAGA[A/T]GTTCTGAAAAGCCCT | 212712 |
rs36752152 | snp | A/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56799898 | CTTTACAACTTTCTA[A/T]TGCTTCATGAAATGT | 212712 |
rs36754014 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56797833 | ACTAATGGCAGACAC[C/T]GCAGTTCAACGTTAG | 212712 |
rs36756482 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Satb2 | Mm_Celera | 1:56851669 | AATCCTGTACTTTGA[G/T]CACACAAAAAGTCAC | 212712 |
rs36762712 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56877506 | CAGTTATGGGTACTG[A/C]GCCAGAATCTCTTAG | 212712 |
rs36764084 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Satb2 | GRCm38.p3 | 1:56853355 | CACTCATCTCTCATA[G/T]AGAGCACCCTTGATG | 212712 |
rs36764858 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56908291 | AATGCCTGCTTTGTG[C/T]CCTTTGGAATATTTT | 212712 |
rs36766300 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Satb2 | GRCm38.p3 | 1:56945364 | GACATATTTGCACTT[A/C]TACTGCTTTTCTAAG | 212712 |
rs36767577 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56884901 | AGCTTGAATCTCCAA[A/T]GTCCTCAAAGGCATG | 212712 |
rs36772231 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56927486 | ATACATCCTGGGTTC[A/T]GGCTTTAAAGGTCCC | 212712 |
rs36773057 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56965838 | CTTTTTGAAAGCATT[A/T]AAAAAAATCCTAGGA | 212712 |
rs36774454 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56823460 | CCTCTGCCTTCTACA[C/T]AGCTAACCACACTCA | 212712 |
rs36777321 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56947520 | ACATAAGCTCCCTGG[A/G]ATTATCAACAGAATA | 212712 |
rs36785494 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56889977 | ACCAGCAGATCATCA[C/T]GTGGCCCTTGAATGA | 212712 |
rs36785978 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56942329 | TCCAAATGACTGCTG[C/G]TGACTGATGTCAGCC | 212712 |
rs36786980 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56803486 | AAACACATACTGCAG[C/T]AAGAAAGCCTGAAAC | 212712 |
rs36792951 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56833197 | ATAAACACAACTGAG[G/T]TTGCGAGAAACAAAT | 212712 |
rs36794768 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56813179 | AATCATTAACACTCT[C/T]GATTGGTGTTCCAAG | 212712 |
rs36795032 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | GRCm38.p3 | 1:56830962 | CTCTCAGGGCATCGG[A/C/T]GAGAGTTAAAGGTAT | 212712 |
rs36795533 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56859625 | GTAAGCTGAAATTAA[A/G]ATAGTAATTATTGTT | 212712 |
rs36797100 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56963492 | AACTCTTCTGCACTT[C/T]CTCAGCTAAGTATAA | 212712 |
rs36797671 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56953550 | TGCGAGGCTTGGAAT[A/G]ACTTCAGAAATGATC | 212712 |
rs36797697 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56944953 | CAATTCAGCTTTTTA[C/T]ATATGTTCAATAGCA | 212712 |
rs36802187 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56834267 | CAACATCCATTGCCA[C/T]GTTTGATTTATATGC | 212712 |
rs36811151 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56837357 | CTGAGCCTCCAGCAC[A/G]TTGCATACTCTTTCA | 212712 |
rs36812550 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56807028 | GAACTGTGGATTGCA[C/T]ATCTCATGCCTAGCT | 212712 |
rs36815113 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56840631 | TATGTAAGACTTGTG[C/G]TAGGTCAGAGCAAGG | 212712 |
rs36817117 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56807056 | GCTGAGAGCTCAGGA[C/T]TTCTTTGATAGCTGC | 212712 |
rs36818609 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56877616 | GGAAGTATCTTAGTA[C/T]GAGTATAAAATGATG | 212712 |
rs36819671 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56943074 | AATTTGACCTTAGGG[A/C]ATTATTTATCTGAAA | 212712 |
rs36836810 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56809988 | AACAGCAAAGTTGAG[A/G]TGAATAACTATGTCT | 212712 |
rs36841382 | snp | A/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56960699 | CTCTCTACTTCTACC[A/T]AAGTGACAAGGTGAT | 212712 |
rs36842394 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Satb2 | GRCm38.p3 | 1:56835825 | CCCTGAAATGGACAA[C/T]CCTAGAGTAAGTGGC | 212712 |
rs36844849 | snp | C/T | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56962434 | TCATTCCGGGACTTT[C/T]TTATTTTGGCTTGAG | 212712 |
rs36849413 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56830478 | AAAGAGATGAGAGCC[A/T]GATAGCTGAGGGGCT | 212712 |
rs36852401 | snp | G/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56883805 | ATCTCACAGAGCACT[G/T]GTAGGTAAGAGCTTC | 212712 |
rs36853510 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56835173 | ATAGGGCCTCATATT[C/T]GCTTGTCTAGTGGCT | 212712 |
rs36854210 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56881338 | TACTTATTAATTATT[A/G]TGTGCCAAGAATCAT | 212712 |
rs36859663 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56801090 | ACAGTTGGGCTACTC[C/T]ACTTCCCCTCGTTTC | 212712 |
rs36859953 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56879184 | ATGCTATATTTGTAC[C/T]AACCAACAGATGGAA | 212712 |
rs36860593 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Satb2 | Mm_Celera | 1:56906850 | CATCAGTGACAGATT[G/T]CCTTATTATTGTTTC | 212712 |
rs36864169 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56968819 | AAAACAGTCTGAATG[C/T]TGTGTAAAGTTGTAC | 212712 |
rs36864417 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56827901 | GAACATATTGTGTGA[C/T]ATTCTAAAGAACTAA | 212712 |
rs36864703 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56873783 | CCAAAATAACAACTT[A/G]ACATGACTTCTTAAA | 212712 |
rs36866317 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56807891 | TTCATCAGACTTCAT[A/G]AATACATGTTCTTAC | 212712 |
rs36867711 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56878340 | CCAGGCCTATACTCA[G/T]TCTTATCGTAAGAAA | 212712 |
rs36871146 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56834517 | GTAGCCAACAAGGCC[A/C]TGTTCTTAGGGCAGC | 212712 |
rs36875486 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56953591 | GCACTACAGACAAAA[A/T]GAGAAAAGACTCTGA | 212712 |
rs36876274 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56940040 | AGACAGACGTACATC[C/T]TAAGCAAATGACTCA | 212712 |
rs36884187 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56854029 | AGCTAAGCAGGAGGT[A/G]TCATTTGGACAGTAC | 212712 |
rs36885353 | snp | A/C | 0.18 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56850134 | AATGTCCATGAAGCA[A/C]GAGTGAAGTATGTGA | 212712 |
rs36893209 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56885937 | TGGATGGATAGAAAA[C/T]TGGTAGCTAAGGAAA | 212712 |
rs36897391 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56836284 | TCTTCAGATGTGGCA[C/T]AGCCATAAAAGACGG | 212712 |
rs36897947 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56876619 | AGGGGCCAGTACAAG[A/T]GAACATCGTTTAACA | 212712 |
rs36897949 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56908202 | CGACTCAACAGATAT[C/T]ATAGCCATTTACTAA | 212712 |
rs36898376 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56863700 | CAGAAGTATAAGGAT[A/G]AATGTGGAGCAACAC | 212712 |
rs36900814 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56941818 | TTCCATTTCTGACTT[C/T]AACAGCTAAATCATG | 212712 |
rs36901235 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56949356 | CCAGGCACTCCATAA[C/T]GAAAACAAGGCCTCT | 212712 |
rs36901504 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56879861 | AATTGGTACCCAAAG[C/T]CTGAGTATAAAACAG | 212712 |
rs36903967 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56811824 | TTAACGCCTGGGAGA[C/T]GCGATTTGTGAACTC | 212712 |
rs36904470 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Satb2 | GRCm38.p3 | 1:56916148 | GTACAGATATAGATC[A/G]GGCTTAACAAGGTTT | 212712 |
rs36905236 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56904262 | TAATATCCTTCCAGA[C/G]TCAAAGAGTTGACGT | 212712 |
rs36905454 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56841340 | GCTGTCCCAAAGGCC[C/T]TGCTGGACAGGCAAA | 212712 |
rs36906424 | snp | C/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56934973 | AAAACACACTTAAGA[C/G]GAGTGGTTAAATGAT | 212712 |
rs36908045 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56829958 | TGTTCCACAGTACTG[A/G]AAAATACAGAGTGGT | 212712 |
rs36912664 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Satb2 | GRCm38.p3 | 1:56909402 | AGCCTCACTGTCATG[C/T]GCATGGATACCTGAT | 212712 |
rs36914475 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56894809 | ATAGCACCTTTGTAC[A/G]TCTCTCACATCTACA | 212712 |
rs36916297 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56946628 | CATTTGGGCATGTCA[C/T]GTGAGATAAAAGTAG | 212712 |
rs36920080 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56911352 | TTCTACCAACTATGC[C/T]GTTTACTTCCAACTG | 212712 |
rs36920103 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56816194 | AGTTTTTCCTGCTCC[A/G]TAGAACCTGACTGCA | 212712 |
rs36920743 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Satb2 | GRCm38.p3 | 1:56916794 | AAGCAGGCAGAGTTG[C/T]CTGGGCGCCATGCAT | 212712 |
rs36921270 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56839083 | CAGAGGACATAGAAC[A/G]TGGAGTCCTGTCCAT | 212712 |
rs36921567 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56854609 | GCAATCTGGCTTGCC[C/T]GATGATACATGCTAT | 212712 |
rs36925513 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56939667 | TGATACTACATGAAT[A/G]AGTGAACATACAGGG | 212712 |
rs36925999 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56811705 | AAGAAAGATGTGCTA[A/G]GTTTTCAGGTTAAAA | 212712 |
rs36928229 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56949171 | GACATGTAATAAACA[C/T]GGACTCTGCCCTGCA | 212712 |
rs36929022 | snp | C/T | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56960278 | AGTGCTAGGGACATC[C/T]GGTGCTTGAGCCTCA | 212712 |
rs36930045 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56882135 | TCAACACAGACACAA[C/T]GAGGCCTGCATCTAT | 212712 |
rs36932543 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56830900 | GAAAAGTGGGAACTG[A/G]AGACAGAAAAGGCTC | 212712 |
rs36933861 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56823848 | TTTTTTAATTAAACA[C/T]ACTGCAATCCTAACT | 212712 |
rs36935914 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56936728 | GCCAAGGGACATCTT[A/C]ACACAGGACTGTCAT | 212712 |
rs36940433 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56895141 | AGCTTAGAGACTGAC[A/G]ATGAGAAAACTCATT | 212712 |
rs36940798 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56875979 | GGGGATGCAACCCTG[A/G]GCCTCTTGCGTGCTA | 212712 |
rs36948967 | snp | A/C/G | 0.391111 | 0.206368 | intron-variant | Satb2 | GRCm38.p3 | 1:56939718 | ACAGAAATGTCCAGC[A/C/G]TAAACCACAGAATGC | 212712 |
rs36950969 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56945947 | TTATTCCAAAAATGT[C/T]ATTCAAGATTTTCCA | 212712 |
rs36951567 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56903209 | CTCTGCACAGCTGCA[C/T]GGAGAGAATCTGTAC | 212712 |
rs36952107 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56872536 | GTGTTGGAAACGCAC[C/T]GGGGATACACCTAAA | 212712 |
rs36953369 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56804650 | CATGAAGGAAGCATC[A/G]TAGGTGTGAGGTCTG | 212712 |
rs36956905 | snp | C/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56818002 | TTGATGAGGCACATA[C/G]TGCTTCGTGACCTTT | 212712 |
rs36957536 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56959865 | GAATTAATGTTTAGG[C/T]TCAAACTGTAAAGCC | 212712 |
rs36962330 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56893848 | GCACAGGGATCTTTC[A/G]GAAATAACGTACAGC | 212712 |
rs36963086 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56832248 | CATCATCGTCATCAT[C/T]GTCATTATTTTGAGC | 212712 |
rs36965249 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56965575 | AGCTATGCTCTTAAA[C/G]AGACCTGGAAGCAAG | 212712 |
rs36971455 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56953615 | ACTCTGAAGGGCCAG[A/G]CTCCACCCTTGTCCT | 212712 |
rs36972156 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56953198 | CTGAAGCACAGGATC[A/G]TCACAGCTGGAGGTT | 212712 |
rs36972750 | snp | G/T | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56830542 | GTCTGTGTCATAAAC[G/T]TTACCTAACCAGCCT | 212712 |
rs36981461 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Satb2 | Mm_Celera | 1:56830083 | GAAGAAGTTAAAAGT[C/T]GGAAAGCCACTGTTC | 212712 |
rs36982223 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56859150 | GATGGCTGAGGTGAC[C/T]GAGAATGGAGCAGGT | 212712 |
rs36982307 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56875446 | TTTCAGTGTCATTTA[C/T]CCAGTAATGAGGAAG | 212712 |
rs36987494 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56953012 | CTAGCAAACCTTAGG[C/T]AGCTACTTGATTGCT | 212712 |
rs36997390 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56853405 | ACTGTTGAAGCAAAA[A/G]ACAGGTAGACAGACA | 212712 |
rs36997822 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | GRCm38.p3 | 1:56854274 | GGTACAGAACATTTT[C/T]CAGGGAGACATAATA | 212712 |
rs37002822 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56822997 | CTTTTCTACTTCCCA[A/G]TCAACTTCTTAAGGT | 212712 |
rs37016840 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56861999 | CTCATAAAAACTAAA[A/G]AGTAGTCAAATGAGG | 212712 |
rs37018944 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56829384 | ATGATAACGTCTGCA[C/T]AGGAATCCAGACAGG | 212712 |
rs37024407 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56819560 | TAGACAGTCAGGAGA[A/G]ACCAGAGTAACTGAA | 212712 |
rs37025503 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56884845 | ACCCCAATGCAGTGC[C/T]ACTCCAGCTTCTTAC | 212712 |
rs37033222 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Satb2 | Mm_Celera | 1:56795111 | GGAGGTCTCCTCTTG[A/C]AATCGCTGTCACTGG | 212712 |
rs37034890 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56891396 | AGCTATGACTCCTCT[A/G]CAAACGAAATGATTT | 212712 |
rs37036111 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56905352 | TAATAATTCAGCCTG[C/T]GCTTCTAACCTGTGG | 212712 |
rs37036889 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Satb2 | Mm_Celera | 1:56918192 | CACAATAAAATCTTT[A/G]AATGACTATTATGCC | 212712 |
rs37037449 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56838795 | CACTTAACAAGCTGG[A/T]CTTATCCTTTTGAGC | 212712 |
rs37039901 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56881737 | ATAGCCAAGAGTAAA[C/T]TAAATGTGTTGCACA | 212712 |
rs37042735 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56823258 | GGACAAAGACAGGCC[C/T]GGGTTCTGATGAGGA | 212712 |
rs37046155 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56808882 | ATGACACATTACTGA[A/G]GTCATCAATTGCAAA | 212712 |
rs37047625 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56962261 | GTTCTTTATGGACTT[C/T]GGTTTGATTTCTCTG | 212712 |
rs37049279 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56812504 | TCCCATCAGTGGCAG[A/G]CCTCCTTGCTAATTC | 212712 |
rs37056466 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56880579 | CCTGTTGTTTAATTC[C/T]CACTACTGTGTGACC | 212712 |
rs37056636 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56825613 | AGGCAAGCAGGGATG[C/T]TAACAAATGCCTGTG | 212712 |
rs37060415 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56934927 | AAACCTGTATCTTCA[C/T]GGCTACTCAGAAGGT | 212712 |
rs37073991 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56949981 | CAGATGTCTCTCACA[C/T]TATCTTTTCATCATT | 212712 |
rs37078250 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Satb2 | Mm_Celera | 1:56796801 | TCTCTGGTCGGTTTC[A/G]GCCGGTGCAGCCTTG | 212712 |
rs37086161 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Satb2 | GRCm38.p3 | 1:56905484 | GGAAAAAAGGAAGAC[A/G]AAAGGCCAGGTTTAA | 212712 |
rs37086499 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56881845 | GGCAATCATTCAACC[A/G]TTTTGGCTCTCCAAA | 212712 |
rs37087762 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56907436 | GCATGTAGATTATCA[A/G]AGAAAAGGTGGCTAC | 212712 |
rs37089280 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56880228 | ATTATGAGATTTATT[A/T]ATTGACCTAGAGGAC | 212712 |
rs37092888 | snp | C/G | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56961893 | AAACGGAGATGGGCA[C/G]GGAGCTCTGTGAAAC | 212712 |
rs37098224 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56898804 | TGCCTCTGCAAACAG[C/T]GTAAAGCAGTTGGAA | 212712 |
rs37101187 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56961091 | AGAAGCACTCTGGTT[A/C]TTCTGCATCGTCTTC | 212712 |
rs37112635 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56806702 | GGAAAGTATTCCTGC[A/G]TCAAAAATTCCAAGA | 212712 |
rs37115521 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Satb2 | Mm_Celera | 1:56959323 | CCATTTCTATGTGAT[C/G]AGATGCCTGTAACAA | 212712 |
rs37115672 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56875930 | CCATGAGCTACTTTT[A/T]TTTTTCAGAGTGGGA | 212712 |
rs37119437 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56942798 | TCTTTACTTCCAAAA[A/G]CTGAAACGGCACTAA | 212712 |
rs37119842 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56829904 | ATGTCTACTCTTGCT[A/T]TGGCCTTTTGCCTGG | 212712 |
rs37120162 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56835587 | CATCTGATCTCCAGC[A/G]ACCAGTAGCTCCTTC | 212712 |
rs37128225 | snp | C/T | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56965725 | GAACAGGTATTTCAA[C/T]AAGACATTCTCAAGG | 212712 |
rs37129986 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56840475 | TATTAATAGCAAAAT[A/G]TACCTTACTACCATA | 212712 |
rs37130223 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56896539 | CTCTACTATCTTCTC[A/G]TAGCCCCACTTGTGT | 212712 |
rs37130318 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56833005 | AATGCAAATGATGGC[G/T]TATATGAAAATAATA | 212712 |
rs37133256 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Satb2 | GRCm38.p3 | 1:56859097 | TTACTGCCTGTACCA[C/T]CTTGAGGAAGGGGTG | 212712 |
rs37134647 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56872830 | TCACAGAGTCAAGCA[C/T]ATAGGATCCGTCTGC | 212712 |
rs37137313 | snp | A/C | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56886112 | TAAGCAACTACCAGC[A/C]TAGCTAAAATGAGCC | 212712 |
rs37137527 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56835227 | TGCTCTTGCATGAAC[A/G]CATCCGTACCTGTGT | 212712 |
rs37148601 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56947810 | ATATCTCAGCACTGA[A/G]CCCGAAAACACCAAT | 212712 |
rs37156654 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56887436 | TGTGAGAACGGAATC[C/G]GTTACACTGCAAATA | 212712 |
rs37159808 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Satb2 | Mm_Celera | 1:56893378 | AGGTGAGGCTGTAAC[C/G]CACAACACTCTGGTC | 212712 |
rs37162270 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56856680 | CATCTCTTATGAAAA[C/T]GTATGATTCAAAAAT | 212712 |
rs37163060 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56952087 | CCTGAGTCACTGACT[A/G]TTCATAATGTATGTA | 212712 |
rs37165472 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56868824 | ACTTATAGGTTCAAT[A/T]TTCTTTGCCAATCTT | 212712 |
rs37168191 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56829076 | CAGGGCAAATTCAGT[A/G]TAGAAAAAATGGCCT | 212712 |
rs37176800 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56948548 | CATGTGGCCCAGGTC[C/G]AGGTGACCTTAGGAC | 212712 |
rs37183807 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56797313 | CCACCAGTCCTTTGC[A/G]GCATGTATTATCTCC | 212712 |
rs37186041 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56804202 | AATATGGTGGGAGAG[A/G]CCCATAGTATGAAAT | 212712 |
rs37191093 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56945462 | CACTATCCTTACAGC[A/T]CGAGTCTCCCTCACA | 212712 |
rs37193468 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56871283 | CTACTCTGACTCTTA[A/C]TCCCCAGAGAGAATA | 212712 |
rs37197021 | snp | A/G/T | 0.231111 | 0.249285 | synonymous-codon | Satb2 | GRCm38.p3 | 1:56796825 | AGCCTTGCTCTTGTC[A/G/T]GCATTCTCTTCCTCG | 212712 |
rs37199361 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56797718 | AAGCCAGCACTGAGA[C/T]TGTGGGGCACTGAGT | 212712 |
rs37201780 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56890227 | CTAGCTGATCTAAAT[A/G]GCATCTAACTTGTTA | 212712 |
rs37218268 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56886023 | TTATTTCTTTTACTT[C/T]ATCAATTCTGTTATT | 212712 |
rs37219354 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Satb2 | GRCm38.p3 | 1:56946348 | CATCACTGAGAGTCA[A/G]TGGGGCTCCCTAGTG | 212712 |
rs37219978 | snp | A/C/T | 0.46281 | 0.131194 | intron-variant | Satb2 | GRCm38.p3 | 1:56916816 | GCCATGCATCAGTAC[A/C/T]AACACATGATCCCAT | 212712 |
rs37221126 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56816235 | TAGCAGAGCAGGTGG[C/G]AGGCCCGCCAAAATT | 212712 |
rs37228233 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56935248 | AAGCCTGGTGAGCTA[A/C]GGACTATGCAGTTGG | 212712 |
rs37229947 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56814978 | TTAAGGTGCTATCCT[C/T]TTAAGGTATTGTACA | 212712 |
rs37234993 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56943537 | ATCCCTGTTCAGAGC[A/C]GGCAGGGCTTCCCAC | 212712 |
rs37240102 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56838500 | CTATAGCCTCGGGGA[A/G]CTACTGAAGGCATTT | 212712 |
rs37240259 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56815300 | CTCTAAACGAAGAAC[A/G]GTACTGCCTCAAGGA | 212712 |
rs37241165 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56955282 | TAGAAATGAAGTGCA[A/G]GGTTAGACAGAAGTA | 212712 |
rs37241741 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Satb2 | Mm_Celera | 1:56795778 | ATTTTAAGATTTGAA[A/G]CCACAAGCGAGTAAA | 212712 |
rs37249530 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56833115 | CGTCGCTAATTTTAA[A/C]ACCAAGAACTGTCCC | 212712 |
rs37251827 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56906628 | GAAGTTGGTATTTTA[C/T]AAACCTTTATTTAAT | 212712 |
rs37253604 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56890821 | TTCCTGATGCGTCAG[C/T]GCTCATTCCAACTTG | 212712 |
rs37255847 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56893508 | GTGAGAAGGCAGGGA[A/G]AAGGTGTCCTCTACC | 212712 |
rs37260899 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56935183 | CCTTATTGAACTCAA[C/G]TCTGCAGCGAGGGTC | 212712 |
rs37272376 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56874690 | CTAAATAGCATTGTT[A/T]AAAAAAATACAGATC | 212712 |
rs37284339 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56943073 | CAATTTGACCTTAGG[A/G]AATTATTTATCTGAA | 212712 |
rs37285649 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56806863 | TGAGGCTTCAACAAC[A/T]TAGTGGCAAGTTTCC | 212712 |
rs37286028 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56904454 | TGTAGCTGAACATTC[A/G]AGAAACCACTTAAAG | 212712 |
rs37287894 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Satb2 | GRCm38.p3 | 1:56945344 | CACTCCAAAATCACA[C/T]TGCAGACATATTTGC | 212712 |
rs37289123 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56806637 | TGTTTTACCTCATCT[A/G]TGCCAATAAACACGA | 212712 |
rs37293368 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56933539 | TGCTAATGCTACACA[C/T]GGAACCATTCACAGC | 212712 |
rs37294028 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56833783 | TGGTTAATTTTCAAG[C/T]GCCATGCACATGAAA | 212712 |
rs37300924 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56817236 | GATTACAGACGCATT[C/T]TGTGTTGAGGGCTGG | 212712 |
rs37302059 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56955927 | AAGCTCGCCAGACCA[C/T]GCGGCGATGCGTGTC | 212712 |
rs37307812 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56957945 | CAACCCTAAACCTCA[C/T]GCTGAAGTATTTTAG | 212712 |
rs37313326 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Satb2 | GRCm38.p3 | 1:56916892 | CCAGAGGACCAAATG[A/G]AAGGAGAAAAGGATT | 212712 |
rs37313501 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56801682 | TAAAATGCTTAGAAA[A/G]GAATGATCTCCAGTG | 212712 |
rs37317977 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56828904 | AAAAGCATTCCCAGC[C/T]GTTTCCAGTGATTAT | 212712 |
rs37320828 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56799763 | TTAAAAAGCAGTCAC[A/G]GCCATCCCTGCTGAG | 212712 |
rs37328215 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56823368 | GTGATGGTTTGGAAG[A/G]AAAGCTTATTAGAGA | 212712 |
rs37333680 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56938937 | AGCACACATTCTCAA[A/G]AACTGGAAGGTGGTC | 212712 |
rs37337033 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56948693 | GTTATAGTTCCAGGC[C/T]TGAGAAGTTATGTGA | 212712 |
rs37339865 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56822356 | TGGCTGTGTCATTCA[C/T]ATGGGATCAGTTTGT | 212712 |
rs37347257 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56813156 | ACAAATGACATTAGC[A/G]GGGAATTAATCATTA | 212712 |
rs37347835 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Satb2 | Mm_Celera | 1:56796354 | ACAGTCTAGTCCTTC[A/G]GATTGTAAAGTTCTC | 212712 |
rs37350012 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56889053 | GTGTTTACTTCACAC[A/T]AACCTTAACCTTCCC | 212712 |
rs37352855 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56832683 | AGGAAAGACAAACAG[A/G]CATATATTATGAGAT | 212712 |
rs37359309 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Satb2 | Mm_Celera | 1:56902084 | AGGGCTGTCTGCCTA[A/G]TGCATTAATCCACTT | 212712 |
rs37363974 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56942621 | AGTAAAGTAGCACCA[A/G]ACTAACAAATAAGTT | 212712 |
rs37366923 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Satb2 | GRCm38.p3 | 1:56911284 | AGCAAAACAATGGCA[C/T]ATATATCAATGAGGA | 212712 |
rs37369419 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56898098 | GGAGAGTGAGTGACA[C/T]GAGGCCCTCGCCCAT | 212712 |
rs37371889 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56834865 | AGCTTGTTGAGAGCC[C/T]GCACTAGTACAAAGT | 212712 |
rs37372648 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56957219 | TACTGTGACTGAGAC[A/G]AAGTTAATAAACACA | 212712 |
rs37378537 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56805644 | ATTGATGGCTGCCTT[C/T]GTCAGCTGTGGCACA | 212712 |
rs37380491 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56904436 | GTTTGGGATATTGCA[A/G]ATTGTAGCTGAACAT | 212712 |
rs37380662 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56840782 | CTGGGAAAATAACGC[A/G]TAAAACAGTTTCCAT | 212712 |
rs37380911 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Satb2 | Mm_Celera | 1:56870875 | TATGCGTGACAGGTG[G/T]ACATGCTTGTGGAGG | 212712 |
rs37382890 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Satb2 | Mm_Celera | 1:56842626 | GGCTTTGTGAAACTA[C/T]GATGGTAGAACTCGT | 212712 |
rs37386531 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56857858 | CAGTCTCACAATTAT[A/T]CCTCTCACCTTCCTT | 212712 |
rs37388693 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56942805 | TTCCAAAAGCTGAAA[A/C]GGCACTAACTCAAGA | 212712 |
rs37389161 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56938590 | CAGGGACCTTAACAT[A/C]TCAGGACCTTTGTTA | 212712 |
rs37393342 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56947687 | GTTTAATTAAAACCT[A/G]ATGCCAAACTGCAGA | 212712 |
rs37408057 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56829763 | TTGAATATAAGGCCA[C/T]GAAAAGTCCCTGGTT | 212712 |
rs37409374 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56872636 | AGTTCAGGAAAATGC[A/T]ACCATAGATGTGTTA | 212712 |
rs37423741 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56800760 | AGGTTAGGGGCTCGG[C/T]TTCTGGTGAGAAAGG | 212712 |
rs37426883 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56946943 | GTGCATATAGAATCA[A/G]AGGGAAGACCTTAAA | 212712 |
rs37435146 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56839518 | CAGCAAATGAACAGT[C/T]CCTCGGAATGACTCA | 212712 |
rs37436905 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56875865 | ATGCATGCGGTGGAA[A/G]CAGTGACTTGGCACA | 212712 |
rs37439582 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56936358 | TGTACCCAGACCCAT[A/T]TCAAACCTGTTAATG | 212712 |
rs37442759 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Satb2 | GRCm38.p3 | 1:56796570 | ATTGTAAAAGTTTAA[C/T]ACTTAGTGTCTTTGC | 212712 |
rs37459605 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Satb2 | GRCm38.p3 | 1:56945717 | GCTATCTCCTTGTCG[A/G]ATAAACTGGCTGTGC | 212712 |
rs37463167 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56877588 | GAACCAATATGCTAT[A/G]TCATCTCTGCTTGGA | 212712 |
rs37464893 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Satb2 | GRCm38.p3 | 1:56897982 | GGCTAATGTGCTCTG[A/G]TTCATTTCTTTGAGC | 212712 |
rs37470049 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56877254 | AGCCACAGGCCAGGA[C/T]AGAATCCTACTCAAT | 212712 |
rs37470965 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56834543 | GCAGCAGAGAACTTC[C/T]TCAAATCCCTGATGG | 212712 |
rs37473005 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56870884 | CAGGTGTACATGCTT[A/G]TGGAGGCAAGACCTT | 212712 |
rs37477981 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56966668 | TAGCTGCTATTGGGC[A/G]TCTAAGGCTGACCAT | 212712 |
rs37479986 | snp | G/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56836751 | AGAAAATAAGCAAAC[G/T]GTTTTTATTAACATT | 212712 |
rs37486162 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56938226 | TGCGTTGTCCATATC[A/G]TTTCATTTTTAGCCC | 212712 |
rs37488923 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56857887 | TTTACATTGGCCACT[A/G]TAAAAACTGCCTCCT | 212712 |
rs37491958 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56873864 | ACCATGTTATTCCCT[A/G]TCTAAAAGTTTTGCA | 212712 |
rs37492104 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56885874 | ATTACAAACTTTTAG[A/G]AACCAGGAGCTTAGT | 212712 |
rs37500388 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56823171 | TTGGGAGTTATCTAA[C/G]GTAGTATATATGGAT | 212712 |
rs37501696 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56916105 | AAGCTGATGGACAGC[A/T]GTGGCCACCACCTCT | 212712 |
rs37509356 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Satb2 | GRCm38.p3 | 1:56794824 | CCTGTATAGTGTAAG[C/T]TCTGAGTTAATATCT | 212712 |
rs37513465 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56799783 | TCCCTGCTGAGACCT[A/G]TGAAGTCAAGTGTGG | 212712 |
rs37514054 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Satb2 | GRCm38.p3 | 1:56917281 | TGACCCTAATTGGTG[A/G]CATTTAATAAATGAG | 212712 |
rs37524290 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56855100 | AGAATGTGAACAAGT[A/G]CTGTGCAGATCCCCA | 212712 |
rs37524354 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56942393 | CTACCACATTAAAAA[A/C]CAAAGCCAGAGAGGA | 212712 |
rs37529822 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56876646 | AACAGTGTTACAGCC[C/T]GTGCCTGCAGAAGCC | 212712 |
rs37533692 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56888057 | AACCAATTTAGGACC[C/T]TTTAAAGAGTATGTG | 212712 |
rs37535039 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56853986 | AAAGCCTTTGCTACT[A/G]TGTCATCTGGCATTC | 212712 |
rs37538780 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56908560 | ATACATAATAGGTGC[A/T]CATTCCGCAGACAAA | 212712 |
rs37541847 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56902121 | CAGTCTCCTTCCCTG[A/G]TTACTTAGAATAGCA | 212712 |
rs37544404 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56917180 | TCCACTACTAAAGAG[C/G]CTTCTAACTCCAGTA | 212712 |
rs37546987 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56829653 | TTTCCACTTTCATCA[C/T]TGACATGTGGCTGAG | 212712 |
rs37548732 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56839130 | TGTATGACTTTGCTA[A/T]TTTTCCTGTATCTAG | 212712 |
rs37549742 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Satb2 | Mm_Celera | 1:56901740 | AAACCATAATTAAAG[A/G]GAGAGGTGTGTTGGA | 212712 |
rs37562607 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Satb2 | GRCm38.p3 | 1:56828801 | CAGCCACAGACAATG[C/T]CATTATGGCTAGGTA | 212712 |
rs37575041 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56819284 | GCATGGCCTTATAAC[G/T]CTACAGTCTCAAAGC | 212712 |
rs37582051 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56862320 | TTCTCAAAGGTGTCT[A/T]TGTCTTACTGCCGGC | 212712 |
rs37583183 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Satb2 | Mm_Celera | 1:56843375 | TGGCCAAGAGCCATA[C/G]CTGCACTGGAAACAT | 212712 |
rs37586164 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56898368 | GACTCTTTATCAGTC[A/G]CAGAAGAACTTTTGA | 212712 |
rs37590025 | snp | G/T | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56834989 | ATCTGAAATGGCAGT[G/T]CATTCTTTGGCCAAT | 212712 |
rs37591827 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56958691 | ATTGGAATCCCATAC[A/T]TCTCTATCAGACAGT | 212712 |
rs37594018 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56879216 | GATGGCACCCTGGAG[C/T]ATTCTCTAAAGTAAC | 212712 |
rs37594338 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56941511 | TCCCTCAAAAGGTGT[A/G]AATTTCTGAACTCTT | 212712 |
rs37598538 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56824024 | CAGGTTTTGCATAGG[A/C]GCTTGGAACGTATCC | 212712 |
rs37611000 | snp | C/G/T | 0.142012 | 0.225474 | intron-variant | Satb2 | GRCm38.p3 | 1:56870871 | GATATATGCGTGACA[C/G/T]GTGTACATGCTTGTG | 212712 |
rs37618099 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56896771 | AGACTTCTATCAAGA[A/C]TCCAGGAACAGTGGA | 212712 |
rs37620331 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56959633 | TATTCTTTTTTACAA[C/T]GTGAACTAATGGAAA | 212712 |
rs37620587 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56835228 | GCTCTTGCATGAACA[C/T]ATCCGTACCTGTGTA | 212712 |
rs37621315 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56832820 | TCCTCCTCGGCTAGA[A/G]TCAAAGACCAAGGTA | 212712 |
rs37628211 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56838830 | TCTATGTGGGCACTG[A/G]TGAGAACTTTCTGTT | 212712 |
rs37632462 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56806663 | CACGAAATACTCAGT[C/T]CAAAAAATAAAAAAA | 212712 |
rs37637793 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56831150 | TTGGATTCCCAGGGC[C/T]CAGTTAGGAAAAGGC | 212712 |
rs37640066 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56822224 | GTAACTGGTCAGTAT[C/T]GACAACAGCCTTCAT | 212712 |
rs37640544 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56878577 | TGTTCATAACTGTAT[C/T]ACAGCGTATCAATTT | 212712 |
rs37644064 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Satb2 | Mm_Celera | 1:56795034 | TAAAATCCAACCGTG[C/T]GGGACTGCTGAGTGG | 212712 |
rs37649894 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56841256 | CTGGCAACCAGAGAC[C/T]CACACCGATGTGGAG | 212712 |
rs37659231 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56886597 | GGCATTGTCCTGACC[A/G]CCGATACCACGGTGG | 212712 |
rs37660291 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56830396 | TGGCTGAGATGTCAA[C/T]ACTGATAAATTGAGA | 212712 |
rs37671469 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56858299 | ACAAGATAATGTGTA[C/G]AGCAGGACATTCTTA | 212712 |
rs37673885 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Satb2 | Mm_Celera | 1:56796761 | CTTGGACCCATCTAT[C/T]GCTCTGCCTGCGGAG | 212712 |
rs37673890 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56880035 | GATACAGAAAATATT[C/T]CAAATAGGAGCTATT | 212712 |
rs37675047 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56944733 | GCAGGAGCTGCATGA[C/T]GTCACAGAAAACCTC | 212712 |
rs37679225 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56877708 | AGAGAAAAGCTATGA[G/T]TTTTACTGAACTTTA | 212712 |
rs37682477 | snp | G/T | 0.5 | 0 | intron-variant | Satb2 | Mm_Celera | 1:56954353 | CTCCCTACTTTCTCA[G/T]GCCCAGCCTTCTGAG | 212712 |
rs37688688 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56857749 | CTTATAAAAGTATTT[C/T]CTAAAGGCCAGAGAT | 212712 |
rs37690061 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56827854 | AGACATACTTATCAG[C/T]CAACAAGCAAAGGGT | 212712 |
rs37691139 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Satb2 | Mm_Celera | 1:56831460 | GGGCTCAGGTGGGAG[C/T]TGGACCACATGCTGC | 212712 |
rs37691556 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56905035 | TCTCAGCAAAAAGAG[C/T]GTCAATAAAAACTCT | 212712 |
rs37694359 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Satb2 | GRCm38.p3 | 1:56935076 | GTACAGCTTCCTTTC[C/T]GTGACCTGAGAAGCT | 212712 |
rs37715762 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56893438 | CTCTAGCCATTCTCT[A/G]GACGCTGTTCCAGCT | 212712 |
rs37715844 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56942485 | CTTTGCCACCTACTT[C/T]CAACAACAGACTGGA | 212712 |
rs37725240 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56823951 | TAGGGCAAAACTTCG[C/T]TGCCATAGCTCCTTA | 212712 |
rs37727028 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56935191 | AACTCAACTCTGCAG[C/T]GAGGGTCTCTCATTT | 212712 |
rs37733526 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56879583 | TCTTTAAGCCACTAA[A/G]ATGCTTATGCAAATG | 212712 |
rs37740958 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56823989 | AGCAAGGGCTGAGAA[C/T]GGAAACTACATTCAA | 212712 |
rs37746894 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56895699 | CTGAGATACATGAAC[A/G/T]TTGTTTGTGGCACGT | 212712 |
rs37749872 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56887382 | TGTGAGTGCCTCACT[C/T]GGCCCATTTCCTTAC | 212712 |
rs37756689 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56934287 | TAAGTAGAATGCATT[A/C]GTAATGTCTCTCAAA | 212712 |
rs37767994 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56936223 | ATTAGGAAAGACTTA[A/G]GATATGGGAAAAAAC | 212712 |
rs37775895 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56947610 | TTTAAAATGAATGGA[C/T]CACATCAAGACTGAA | 212712 |
rs37776486 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56886219 | ATGTCACTATCATAT[A/G]CTGCTGATTGGACCA | 212712 |
rs37778875 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56857139 | AACCAGTTATGATCA[A/G]TGCCCTCTTAAGAAG | 212712 |
rs37779535 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Satb2 | GRCm38.p3 | 1:56805728 | AACAAAGTAGATCCA[C/T]GCATCAAATATCTGG | 212712 |
rs37780192 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56891105 | AGCAAAGAACTAATA[A/G]CTCATTACCTGAGAA | 212712 |
rs37781995 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56942141 | TCATCCATTTAGCAC[A/G]TGCACTGAACTGTAG | 212712 |
rs37782745 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56836697 | GCAGTTCAAAGACTG[A/G]TTCCTGGCAACCAAC | 212712 |
rs37792166 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56948075 | GGAAAGAGAGAAGGA[A/T]TACCTTGGGCCTGCG | 212712 |
rs37797654 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56889527 | CAAAAAGAAAACTCG[C/T]AGAGGACACTTTAAG | 212712 |
rs37798437 | snp | A/G | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56960636 | ATGCAATAGTTTACA[A/G]AACTCAGAATGAAAG | 212712 |
rs37804805 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56805518 | CCATGTACTAAATCC[A/G]AAGTATTCAGCATAT | 212712 |
rs37807302 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56894902 | TGCTCTGTATGTTCA[C/T]GTGATTCTGATGGAA | 212712 |
rs37810393 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56889539 | TCGCAGAGGACACTT[A/T]AAGAAAAGAAAGCCT | 212712 |
rs37813511 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56964035 | ATCTTAGTGAGTTAT[A/T]TGTTTCCTGCTATGA | 212712 |
rs37817046 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56857998 | AAGAAAACACTTATT[C/T]ATTACAGTTCTGGGA | 212712 |
rs37822245 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56860425 | CTAAAGGTAGTGTTT[C/T]CATTTCCTCTGTGAA | 212712 |
rs37823669 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56892120 | ACACATGTCTGTTTC[A/G]TATGGACACTTGATT | 212712 |
rs37825306 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56817565 | CTCTTCATAACAGAG[A/G]GGACAATTGTGCCTA | 212712 |
rs37861918 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56944694 | ACTGCTGGGTGACCA[A/G]TGATTAAAGAATCTC | 212712 |
rs37868166 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56953171 | CTCAGCCCGGAGAGA[C/T]GGAAGATTGGCCTGA | 212712 |
rs37868710 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56829940 | TTTCCTGGATATGCT[C/T]AGTGTTCCACAGTAC | 212712 |
rs37869831 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Satb2 | Mm_Celera | 1:56917920 | GACAGTAAGACAGGA[G/T]TATAGAAAAAAAGCA | 212712 |
rs37871851 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56805583 | GGAAACATTAGTGTA[A/C]AGTAGCCAGAACTGA | 212712 |
rs37875543 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56942439 | GGTAAGGAACTGACA[A/T]TGGAGCAAAGATTTC | 212712 |
rs37877873 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56906676 | TCCTGAAAAACAACC[A/G]AAATATCAGACAGGC | 212712 |
rs37885128 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56797865 | CTCTCTGCATAGCTG[G/T]CGGAGCTGGGCAAGT | 212712 |
rs37888440 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56820764 | ATTTCAGCTGCAATG[A/C]ATCTCAGGATAAGGG | 212712 |
rs37890480 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Satb2 | GRCm38.p3 | 1:56911892 | ACATCTGATTCATAA[A/G]TTATGACACAACAGA | 212712 |
rs37916260 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56853698 | GATTTTTTCACTTTG[A/G]CTACTTTCACTTTGT | 212712 |
rs37916600 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56957162 | CTGATAGCTCCCTCC[A/G]GGGACAATGAGATCT | 212712 |
rs37918086 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56832807 | GCTAATAGAAACATC[C/T]TCCTCGGCTAGAGTC | 212712 |
rs37919589 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56802738 | ATTTATATATGACTA[A/G]CTGGGTTATTTTAAT | 212712 |
rs37924752 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56949502 | CGAAAAGCAGGCACT[C/T]TTGCAGACTCCTGGC | 212712 |
rs37945083 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56942598 | TAACTAAACTGAATT[A/T]AAAACTAAGTAAAGT | 212712 |
rs37946475 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Satb2 | Mm_Celera | 1:56878346 | CTATACTCATTCTTA[C/T]CGTAAGAAAACTTTT | 212712 |
rs37946901 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56889760 | TACTTCCTTTTACAT[A/C]GTATATTTAGCATAA | 212712 |
rs37948284 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56831778 | ACATTTATTGAGTGT[C/T]CACTGAGCACTGGGC | 212712 |
rs37963218 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56877426 | CACAGTACAGGTCTG[A/T]GAGTCAGCAGATATT | 212712 |
rs37964680 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56893877 | GCAAAGGTCATGGTG[C/T]ATGGAATCATCCCAT | 212712 |
rs37964683 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56956700 | TTCATAGCACAAGCA[C/T]GTTTCCTTTGGGGAG | 212712 |
rs37965641 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56876780 | TTTACTCCGAGCAAC[C/T]GCACCGCATAGCCAG | 212712 |
rs37969784 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56938916 | TATTTACCATCTAGG[C/T]TCTGGAGCACACATT | 212712 |
rs37971195 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56960823 | GAGGACTTTGTAAAG[A/G]CTTGCTGGCTGGTAC | 212712 |
rs37974058 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56830658 | ACTAAGTCCGAGAGA[A/G]GTCTTACACGAGCCC | 212712 |
rs37974298 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56870562 | GGTGACTTTGTATCA[C/T]GACTGAAGACTATTA | 212712 |
rs37984667 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56833049 | CATCGCTCACTGACT[C/T]GTGTCAAAATATTTT | 212712 |
rs37985352 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56895913 | GGAAGGAACCTAGAG[C/G]ATTCTAAAAGCTAAT | 212712 |
rs37986920 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56830123 | CAGTACACTGGTCTA[A/C]TTATCTGTAGGGATG | 212712 |
rs37999343 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56905020 | ACTCCCTGGAAAAGA[G/T]CTCAGCAAAAAGAGT | 212712 |
rs38003709 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56917892 | AGTTAGCAGCAGCAA[C/T]CACTGGGATGGGGAC | 212712 |
rs38013235 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56817718 | AAAGATGTGAATGGC[A/G]AACAAGTTTTTATTT | 212712 |
rs38014639 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56881959 | CCCTGAAGTCTTTTG[C/T]TGTAAGTAGTTCTTT | 212712 |
rs38027214 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56838915 | GACAATGTCCATTTC[A/C]GTTTCTAACTACCAC | 212712 |
rs38038784 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56853118 | TCACATAGTGTTACA[A/G]CAAAGGCTCTTACAT | 212712 |
rs38049546 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56857940 | TGATTCTCTATATTT[C/T]GTGCTTGGTGATGAG | 212712 |
rs38051453 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56801641 | TGGTACTTGCCAATG[A/G]CTGTCTGCCTCCCAA | 212712 |
rs38070240 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56868478 | GCTGGTCCTAGGCAG[C/T]TGTAAGTCCATAATA | 212712 |
rs38072394 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56799151 | AGCCTCTAGTCAGTG[A/G]TAATCATTGTCTTCT | 212712 |
rs38079504 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56805880 | TTACAAGTTCAAAGC[A/C]TGATAAAGTTCCTTT | 212712 |
rs38080527 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56881698 | GTAAATTTTGTATGT[A/T]GAAGGTGAAGGTATT | 212712 |
rs38080883 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Satb2 | Mm_Celera | 1:56947919 | GTTGGTTTTTGTGGC[A/G]CTGGACAAATACTTC | 212712 |
rs38088012 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56937891 | AAGACCATGAGAGTA[A/G]ATGGCACCCATTCCC | 212712 |
rs38092873 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56804816 | CAGCTCAATGGAGGA[C/T]GCTCTCCCATGCAGT | 212712 |
rs38104625 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56916391 | TACTTCCTGTTAGGA[C/T]AAATAATTTGCCTAT | 212712 |
rs38124485 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56821962 | TACAGCTTAGAAGAA[C/T]ATCTGCTACCCTGCT | 212712 |
rs38129335 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Satb2 | GRCm38.p3 | 1:56848716 | AGGACGTGACAGAAG[A/G]TGATCCACGATTACA | 212712 |
rs38134607 | snp | C/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56836881 | AGCGGTCAAGGTATC[C/G]TTTGTTTACAATCCA | 212712 |
rs38140646 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56870465 | AACACCCAGCCAATC[A/C]GTGGGAAAATGCTTG | 212712 |
rs38140782 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56807808 | CAACAATTTCAGTAA[C/T]TGGCCCTTTCACCTT | 212712 |
rs38143051 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56866559 | ATTGGCTTCTGCATC[C/T]TGAGCAATTAATCAC | 212712 |
rs38146399 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56937595 | CCAGAGATTTGTGTT[A/G]TCTTTCTACTATTTA | 212712 |
rs38151943 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56896809 | TGGCTTTAGAGTTAT[A/G]TGTCCTCCCTTCCAC | 212712 |
rs38162932 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56819477 | ACGAATGTCATTTAA[C/T]TCTTCCCCACAGAGG | 212712 |
rs38165294 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56935264 | GGACTATGCAGTTGG[C/T]CTGATCTTTTACTTT | 212712 |
rs38166476 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56876751 | TGAGCAGACATTAGT[A/T]CCCCAGGTATGGCTT | 212712 |
rs38166811 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56886204 | CCATTCTTCTGCTTC[A/C]TGTCACTATCATATG | 212712 |
rs38167545 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56854643 | CAGATAAAAGGAAGA[A/T]ACTAGCTGGGCAGTG | 212712 |
rs38168517 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56935434 | CTGTGCTAATTTAAA[C/T]TGCAAGTAGGTACAT | 212712 |
rs38174346 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56949406 | ATAGGCCCAAGGCAC[A/T]GATGTATAGAAGGCT | 212712 |
rs38181577 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56860313 | AACCCTAGCCAAGGT[A/C]CTCATTTCAGCTAAT | 212712 |
rs38181959 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56837050 | GAGGGTTTTATTGCT[A/G]AGTTGCAGGAAGGAG | 212712 |
rs38182104 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56831678 | AGGACTGCAGGGTGT[A/T]CAGCAGCTATATGGG | 212712 |
rs38184906 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56839253 | GGCAAGTCTTAAGTC[A/G]GTCTGGATTTTGCTT | 212712 |
rs38191576 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56876686 | CCTCAGCGCTGATGT[C/T]CACCTCAGGGCACAG | 212712 |
rs38214534 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Satb2 | Mm_Celera | 1:56794745 | GTACAGGAAAAATGT[C/T]CCTTTGAAAACTCCA | 212712 |
rs38216670 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56819006 | GTCCTCTCTCTCTTC[G/T]GCCTCCTGGCTTATG | 212712 |
rs38218177 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56813927 | AGTCGAGTTTAGCAC[C/G]CTGACATTGTTTTTC | 212712 |
rs38244134 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56946676 | TTTATTGGAGATCAA[A/G]TCCTGAATCCCTCAC | 212712 |
rs38246787 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56941196 | GTATGACATCCCAGC[C/T]AACGTCACTTTGGGG | 212712 |
rs38250264 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56955548 | TACCTAAATAACAAA[A/G]AATGAGCGACACCAG | 212712 |
rs38251871 | snp | G/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56812403 | GAAGCAGAGGTCTCT[G/T]AGCCAAGATTCCTGG | 212712 |
rs38253167 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56839937 | CTGTCAAGGACTTCA[A/G]TGAGTCTCTGCTGAG | 212712 |
rs38258894 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56893735 | ATGAGAAAGAACTGA[C/T]TGAGTTTGTGATACA | 212712 |
rs38263623 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56869233 | CTTAAAGTTCAAAAT[G/T]TTTAGCAAGTTCTTA | 212712 |
rs38263672 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56827844 | GTTACATCAAAGACA[C/T]ACTTATCAGCCAACA | 212712 |
rs38288273 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Satb2 | GRCm38.p3 | 1:56902069 | GCCGTCCCTTCAAGC[A/T]GGGCTGTCTGCCTAG | 212712 |
rs38315159 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56885390 | CCCTGAAAAGCCATG[A/G]GTTCTCACACCCATA | 212712 |
rs38315901 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Satb2 | GRCm38.p3 | 1:56947366 | TCACTTCACCTGAAA[A/T]ACAAGGACAATAATT | 212712 |
rs38317466 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56858933 | AGAGACAAGTAAAGC[A/G]TGAGCTGTCCACAGT | 212712 |
rs38321807 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56968495 | AGGAAGGCTGCTTCT[A/C]GGGACAAATGGCCAA | 212712 |
rs38350383 | snp | C/T | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56963894 | CAAATGCTCTGTCTT[C/T]AAATATGTTCCAAAA | 212712 |
rs38354446 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Satb2 | GRCm38.p3 | 1:56900559 | ATGAAAAGTGCACAG[C/G]ATGCGGCTCAGCTCA | 212712 |
rs38368010 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56905143 | CTTGCAAAACCAGGA[A/G]AACTGGCATTGATCG | 212712 |
rs38371460 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56877269 | TAGAATCCTACTCAA[C/T]TGAATCCTATTCACA | 212712 |
rs38401582 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Satb2 | GRCm38.p3 | 1:56809941 | CCAGTGAAGTAATTC[C/T]TTCATACAACTGAAT | 212712 |
rs38402681 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Satb2 | GRCm38.p3 | 1:56826099 | ATGTTTTAGTTTTGC[A/G]TTGTTTCCCTTGTCA | 212712 |
rs38422570 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56882552 | GCATCCACTATAAAG[C/G]AACTGGGATATGGAC | 212712 |
rs38427541 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56946733 | AAGGAAGCCACCCTT[C/T]GTTATGCTGCTGGGA | 212712 |
rs38456742 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56898497 | TGAAGGACAACATTG[C/G]TTAAGACACAACTTG | 212712 |
rs38456983 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56967455 | CACTGCAAAATTTGA[A/T]ATTCTAAGTTATATT | 212712 |
rs38462121 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56887326 | AATATTTTAATATGA[A/C]GCTATTTGAATTCAC | 212712 |
rs38466571 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56797351 | CGCACTTAGATAAAG[C/T]CAAATCTTGGGAAAG | 212712 |
rs38470951 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56821763 | CATGTGTGTGCCCAA[A/G]TGTGTGTGAGTGTGC | 212712 |
rs38472598 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56824614 | CTTGGTTTTTTACAA[C/T]GAGTACAGATGATAA | 212712 |
rs38483228 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56875751 | CAGCTCCTGACAGCT[C/T]TATCAATAAAATCCA | 212712 |
rs38506963 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56797844 | ACACCGCAGTTCAAC[A/G]TTAGACTCTCTGCAT | 212712 |
rs38510115 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56797896 | CTTTGAGCCTCCATC[C/T]CATCCTGTGTCAGAG | 212712 |
rs38517206 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56953956 | GCCCAAGAAAGACGG[A/G]AGAAATTCAGGAAGC | 212712 |
rs38517215 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | GRCm38.p3 | 1:56839036 | AATCTCTAAAGTTTA[A/G]GTCTAAGTACTACAG | 212712 |
rs38518893 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56909064 | ACACAATGGCCAGAA[A/G]ACTAAGATCTACCCA | 212712 |
rs38529498 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56875567 | TTCCTCTTTTTTTCT[A/G]ACTTTTATGAAGACT | 212712 |
rs38532199 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56831287 | TCTATTTAATTATCT[G/T]AGCGACCTGCTGTCA | 212712 |
rs38557343 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56865869 | CTGTCTTTTGTCCTG[C/G]CTCATTGGAGAGTCT | 212712 |
rs38568637 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56894585 | GTTTTTCAGGCATAC[A/T]CTGGTAAACAAATCT | 212712 |
rs38581313 | snp | A/C | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56905305 | TATTTATCCATAAAT[A/C]AGTTCACAGGAAATC | 212712 |
rs38603002 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56837505 | CCTCAAAGTCAGTTT[C/G]TTAAAGAGGAACACC | 212712 |
rs38611702 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Satb2 | GRCm38.p3 | 1:56818550 | AGTCTAACTAATGTA[A/G]GCTGTTCAGAGTCAT | 212712 |
rs38618807 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Satb2 | GRCm38.p3 | 1:56916718 | TAGATTCTGCACCCA[G/T]AAACTGGATCCCACT | 212712 |
rs38624749 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56892533 | TAAAGAGGATGACAA[G/T]GAACCAAAGTAAGCA | 212712 |
rs38640766 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56818666 | TGACACTCACTGAGA[C/T]AAAATAGATGAAGCA | 212712 |
rs38641912 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56885580 | CGCATGGAAGGAGAA[A/T]CCATATCTTACATAT | 212712 |
rs38648369 | snp | C/T | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56890028 | GACTGTGAACACCAT[C/T]GTATAGTCAGATGGA | 212712 |
rs38665763 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56828876 | AGGCTGTGTTGGCTG[C/T]ATTCTCTAGTTTAAA | 212712 |
rs38669088 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56840947 | CATAAACAGGCAAAA[C/T]ATGTCAACTCAAAAT | 212712 |
rs38680424 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Satb2 | Mm_Celera | 1:56962200 | CCTGCTGTACACTGA[C/T]TTGACTCTCTAATAA | 212712 |
rs38696621 | snp | C/T | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56916142 | TGACAGGTACAGATA[C/T]AGATCAGGCTTAACA | 212712 |
rs38700956 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56832624 | TATTTTCAGCCATAA[A/T]TTTTTACAATACCCA | 212712 |
rs38724148 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56880472 | TTGAAAAGTGTGTTG[A/G]TATCTCAGGTACCAG | 212712 |
rs38726120 | snp | G/T | 0.473373 | 0.11227 | intron-variant | Satb2 | GRCm38.p3 | 1:56895050 | TTAAACTCACTTGTT[G/T]GTTTGATTTTTTTAA | 212712 |
rs38743299 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56829672 | CATGTGGCTGAGATG[A/C/G]TTCTACCTGCTGCTA | 212712 |
rs38763378 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Satb2 | GRCm38.p3 | 1:56936096 | CAGGAGCCACCCGCA[A/G]AGTCATAGACAAAGA | 212712 |
rs38798615 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56817913 | ACCAAATTTCTAAAA[A/T]TGTAACAGGCTGCCT | 212712 |
rs38801396 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56913212 | CATGAGCATATTCTA[A/G]GAACCCTGTGAACTA | 212712 |
rs38808020 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Satb2 | GRCm38.p3 | 1:56903075 | TTCTTGCTCTGAACA[A/G]ACAGCACACTTTGTC | 212712 |
rs38812016 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56946868 | GGGAAAATATGCTTG[A/G]CCACCCTGGTAGAAC | 212712 |
rs38841986 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Satb2 | GRCm38.p3 | 1:56915516 | AGAGAGAAGGCGAAA[C/G]CTGCAATATAGGCAC | 212712 |
rs38887388 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Satb2 | Mm_Celera | 1:56885453 | GAATACTGTCACTCA[A/G]CAGGTAAAGAACAGG | 212712 |
rs38894333 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56821931 | GGACTTGTGTGCCAT[C/T]ATGAGACTGAATATG | 212712 |
rs38902658 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56963741 | TCTCCCACAACTCAC[A/G]AAATACTATGAAACA | 212712 |
rs38922317 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56833717 | TTGCTTGCAAATGTG[C/T]TTTCCAAGTACTTCT | 212712 |
rs38925517 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56851131 | ATGTCTTGATCGACT[C/T]GATGTTTTCTGAGTT | 212712 |
rs38926342 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56821929 | CAGGACTTGTGTGCC[A/G]TCATGAGACTGAATA | 212712 |
rs38932891 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Satb2 | GRCm38.p3 | 1:56825984 | CCACTGGTCCAGTGC[C/G]TCAGGCCATAGTAAC | 212712 |
rs38947530 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Satb2 | GRCm38.p3 | 1:56945839 | GTGACTCCTGAGACC[C/T]GATACAGCCTTTCAG | 212712 |
rs38954439 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56838742 | ACTGTTGGGGGTTGT[C/G]TAAAAAGAATGACAT | 212712 |
rs38983572 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56824207 | ACAGGATATCTTTCT[C/T]GGTGCTGAGAACATC | 212712 |
rs38995913 | snp | C/T | 0.18 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56851712 | TGGTAAAGCTCTGCA[C/T]GTGCCAACGATGCTT | 212712 |
rs39015062 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Satb2 | GRCm38.p3 | 1:56943291 | CAATGCTTTCAAAAA[G/T]TATCTCTACATGTTT | 212712 |
rs39016962 | snp | A/C | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56823093 | GCGTCTGTGGTACTG[A/C]TTGGAAATTCATGCC | 212712 |
rs39050337 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56963063 | TGTTTCTTCAGAAAA[G/T]AGAGAACAATACAAT | 212712 |
rs39089381 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Satb2 | GRCm38.p3 | 1:56900615 | GACCCCTGGACAACC[A/G]CCCTGGAGCAGGCTG | 212712 |
rs39092559 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56812451 | AGTGTCAGATGAGGG[C/T]GCATCAAAGGCGGGG | 212712 |
rs39097835 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Satb2 | Mm_Celera | 1:56817770 | GACATGTATTCAGTT[C/T]TGTATTGGTGTTTTA | 212712 |
rs39117135 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56947462 | TGCATCTTTGGCATA[A/G]CAGAACAATAGAGTA | 212712 |
rs39126335 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56897374 | CCCTGGAGTGCTTGT[G/T]TCTTATGTTCACAGT | 212712 |
rs39128042 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56811376 | CCTTTGAAGATAGAT[C/T]TAAGGCACAGACAAT | 212712 |
rs39210098 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56897155 | TGGCCAGACAGAACA[A/G]CTAAATCATGACTTC | 212712 |
rs39211930 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56897440 | CATTGTTTCTAATGA[A/G]GCATTTTTGTGTGGT | 212712 |
rs39251969 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Satb2 | GRCm38.p3 | 1:56863900 | AGTTATACAAGTGCA[A/G]TGATACAAATACACT | 212712 |
rs39265723 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | GRCm38.p3 | 1:56916444 | CACATTTGTCTGACT[A/G]GGGAGCAGCAGGGTG | 212712 |
rs39271093 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56821591 | TAAGGGAGGAGCAGA[C/T]ATACTATTTATGTAT | 212712 |
rs39271616 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56877498 | TTTAGAAACAGTTAT[A/G]GGTACTGAGCCAGAA | 212712 |
rs39276247 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Satb2 | Mm_Celera | 1:56894762 | TCCTACATAGTGAAG[A/T]TTACTGGAAAACCAT | 212712 |
rs39303815 | snp | C/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56807313 | GGGTTATAAAATTCT[C/G]GTTTCAAGGCAGTTC | 212712 |
rs39306660 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Satb2 | GRCm38.p3 | 1:56915052 | AGCAACTGTCAATGT[A/G]CCTAATACAAACCAG | 212712 |
rs39336898 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Satb2 | Mm_Celera | 1:56945158 | GAATCCCTGGACTCT[C/G]TTTCAGTAGAATTCC | 212712 |
rs39358352 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56838920 | TGTCCATTTCAGTTT[C/T]TAACTACCACAGGCT | 212712 |
rs39363093 | snp | A/G | 0.32 | 0.24 | intron-variant | Satb2 | Mm_Celera | 1:56828186 | TGAGCTTGGTGGACC[A/G]CATCTTCTGACTCTC | 212712 |
rs39413107 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56885464 | CTCAACAGGTAAAGA[A/G]CAGGACCTTTCTCTG | 212712 |
rs39449850 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56835721 | ATAAACTGGGATTCT[A/C]TGAGTTTCAAGGGTG | 212712 |
rs39473806 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Satb2 | Mm_Celera | 1:56840579 | GTTAAACTTTATGCT[A/T]AGCAAACTTCCTTCA | 212712 |
rs39552332 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Satb2 | GRCm38.p3 | 1:56915547 | CGCAGAGAAGGCAGC[A/T]GGATGCCACCCTACA | 212712 |
rs39574221 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Satb2 | Mm_Celera | 1:56869922 | CTTGATGGTCCCTCA[C/T]AAGAGAGAACATGTG | 212712 |
rs39578443 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56890747 | AGCCTGGTTGGTATA[C/G]GATTCAGGGTTTGTC | 212712 |
rs39676536 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56899535 | AATTGGATTGAAAAA[A/T]TTTTAAAAAAGACTG | 212712 |
rs39730473 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Satb2 | Mm_Celera | 1:56886324 | CCTGAAAACCAGCAA[G/T]ATAGAAATGGCTGGT | 212712 |
rs39781150 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Satb2 | Mm_Celera | 1:56909264 | TTGGCATGGATGGAA[A/T]GAGCAATATGGCAGG | 212712 |
rs40013318 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Satb2 | Mm_Celera | 1:56868959 | CAGACACCAGGCTCA[C/T]CCTGAGACCATCATT | 212712 |
rs40055998 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Satb2 | Mm_Celera | 1:56854353 | ATGCTGCCTGCAAGG[A/G]CAGGGAATACAATGT | 212712 |
rs40173492 | snp | A/C | 0.375 | 0.216506 | intron-variant | Satb2 | Mm_Celera | 1:56963612 | TCAATCCAACATTTC[A/C]CTGCTGTTCCTGTTC | 212712 |
rs45860003 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56811946 | AGAATGCTGAACACA[C/T]TTGGTTCCTTATTTG | 212712 |
rs46279389 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56859109 | CCATCTTGAGGAAGG[A/G]GTGTGTCTTCCAAAC | 212712 |
rs46459955 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56842442 | CAGGCAAGTCAAACT[A/G]TAATTTGTTAAGCTG | 212712 |
rs47038894 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56944327 | TTTAAATAAAATTTA[C/G]CAGACAGAAGCACAC | 212712 |
rs47352574 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56842252 | GTTCAAGGCCAGCTA[C/T]GTACTGAGACCCTAT | 212712 |
rs47633345 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56842571 | AGAAACCCACTTACA[C/T]GTGAGCAGACACAGT | 212712 |
rs48653443 | snp | G/T | | | nc-transcript-variant, intron-variant | 9130024F11Rik, Satb2 | Mm_Celera | 1:56974056 | TGAAAGAAAGAAACT[G/T]TAAGTTTGATTTACA | 212712 |
rs48693245 | snp | C/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56919294 | GCAGGAACTCAGCCC[C/T]CCTTTCCTCTGCCTG | 212712 |
rs49682188 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56900922 | CCCTGACCATGAAGG[G/T]AATCAGAAGACTAGG | 212712 |
rs49818607 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56833822 | ATAAATTTTTATCAC[C/T]ACCAGAAAATAAATT | 212712 |
rs50439511 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56944415 | ACCTGGGTTCGGTGC[C/T]CAGGACCCACATGGT | 212712 |
rs50673724 | snp | A/G/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56925773 | ATCATAAAAGAAAGC[A/G/T]TTAAAAGCTGTGATG | 212712 |
rs50903373 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56842613 | CATGCAAAACACAGG[C/T]TTTGTGAAACTACGA | 212712 |
rs51827973 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56957559 | GGCTAGTCCCCCAGT[A/G]CTCCTCCCTGAAAAA | 212712 |
rs52041331 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56944469 | GGAATCTCATTCCTC[A/G]GACTGCTACAGGCAC | 212712 |
rs52516727 | snp | A/G | | | intron-variant | Satb2 | GRCm38.p3 | 1:56880798 | AAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAGAAG | 212712 |
rs107599085 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56867585 | GAACTTAGATCTAAG[C/T]ATGGTTAGAATGGTA | 212712 |
rs107766095 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56960292 | CCGGTGCTTGAGCCT[C/T]AGTGCTTCTCTGCGA | 212712 |
rs107823265 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56926241 | GTTTAGGGGGAAAAA[A/T]TGCTCGTTTATGTCT | 212712 |
rs107825126 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56867592 | GATCTAAGTATGGTT[A/G]GAATGGTAATCTCAG | 212712 |
rs107839332 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56876842 | CCCCTTTTCCTTTCA[A/G]GACAGGGTTTCTCGG | 212712 |
rs107848606 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56877122 | GGGAGAAGGGAGAGC[A/G]CAAGTGCTTATATGC | 212712 |
rs107870234 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56926094 | AAAGATCTCACTTGA[G/T]CCATATTACTATGGA | 212712 |
rs107952820 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56926329 | TGCTACCCAGGGGCA[A/G]TCAAGTGTACTGATG | 212712 |
rs108017608 | snp | C/G/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56926247 | GGGGAAAAAATGCTC[C/G/T]TTTATGTCTTTGCCA | 212712 |
rs108176750 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56877072 | ATATAGAATATATAT[A/G]TGTGTGTATATATAT | 212712 |
rs108286466 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56867533 | ATAGGTAGATACAAG[A/G]GCAGTAGGTTCCTGA | 212712 |
rs108310345 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56917212 | GTTGGATAAATCTTT[A/C]TGTCCTACATATCTG | 212712 |
rs108351671 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56876891 | GGAACTGGTTCTGTA[A/G]ACCAGGCTGGCCTTG | 212712 |
rs108374050 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56867598 | AGTATGGTTAGAATG[A/G]TAATCTCAGGACAAG | 212712 |
rs108388095 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56926359 | GTGCCCTCTATTTGT[C/G]TGTTTTTATATGCCT | 212712 |
rs108417921 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56877043 | ATTAGAAAATATTTA[C/T]ATACAGATTATGCAT | 212712 |
rs108434891 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56876787 | CGAGCAACTGCACCG[C/T]ATAGCCAGAGAACAT | 212712 |
rs108443671 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56960313 | TTCTCTGCGAGAGGC[C/T]GCTGGGGCCTGACTC | 212712 |
rs108521644 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56867125 | ATGAAAATCAGAGAC[A/G]GCAAGAGTCTGGTAG | 212712 |
rs108534475 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56816148 | TGTATCTGCTCAGAA[A/G]GGGTTAAGGAAAGAG | 212712 |
rs108546708 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56877080 | TATATATATGTGTGT[A/G]TATATATACACACAT | 212712 |
rs108552302 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56926144 | AATCACTTACTCTCC[A/G]CTTCCACAGACCTCT | 212712 |
rs108560862 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56867560 | CTGAGTTCAAGGTCA[C/G]CCTAGGACAGAACTT | 212712 |
rs108669897 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56867049 | CTTATTTATATATGA[C/T]TATACATATTTTAAT | 212712 |
rs108684377 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56867483 | AAAAGCAGAAGCAAC[C/T]GCATTATAAGCCAGC | 212712 |
rs108697447 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56926251 | AAAAAATGCTCGTTT[A/C]TGTCTTTGCCATCAT | 212712 |
rs108724874 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56867498 | CGCATTATAAGCCAG[A/C]TGGTCAGAAAGATAA | 212712 |
rs108851875 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56877103 | ACACACATATATATG[A/G]AGAGGGAGAAGGGAG | 212712 |
rs108857491 | snp | A/G | | | intron-variant | Satb2 | GRCm38.p3 | 1:56867477 | ACCCAGAAAAGCAGA[A/G]GCAACCGCATTATAA | 212712 |
rs108917850 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56867305 | CTGGGAGGCAAAGGT[A/G]TGTCTTCCTCTCAGC | 212712 |
rs211716070 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56804653 | GAAGGAAGCATCGTA[A/G]GTGTGAGGTCTGAGG | 212712 |
rs211723125 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56934795 | AGATGTGTATGCATG[A/G]AATGAGTTAACCTAT | 212712 |
rs211736283 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56943025 | CGTAGGCCAGAATTG[A/T]TAAGAAACATGTTTT | 212712 |
rs211737648 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56869535 | AGCTTCAGTCTCACA[A/G]TTTTTAACTCAATAT | 212712 |
rs211755117 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56818028 | CCTTTCTCTCTGCAA[A/T]CCCTTTGCTTGGCCT | 212712 |
rs211762650 | in-del | -/AAACAAAC | | | intron-variant | Satb2 | Mm_Celera | 1:56909006 | CCTAGGAGTCCCACA[-/AAACAAAC]AAACAAACAAACAAA | 212712 |
rs211773742 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56943793 | TTACCTCATTCCCAA[A/T]GGTGAAAATAGCAGG | 212712 |
rs211774845 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56877049 | AAATATTTACATACA[A/G]ATTATGCATATAGAA | 212712 |
rs211798903 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56950567 | AGGTGTCTATAACAT[A/G]TAAGAAACTGATGTT | 212712 |
rs211823596 | snp | A/C/T | | | nc-transcript-variant, intron-variant, utr-variant-5-prime | 9130024F11Rik, Satb2 | GRCm38.p3 | 1:56974717 | TGGCTAGATTCTACA[A/C/T]CCTTTCAAATTCATT | 212712 |
rs211825268 | snp | C/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56907986 | CAATTTTTTCTttca[C/T]ttatttatttattta | 212712 |
rs211847806 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56897081 | TTTATGCATGCTTGG[A/G]GAGGTGAAATAAAAA | 212712 |
rs211862585 | in-del | -/GG | | | upstream-variant-2KB | Satb2 | Mm_Celera | 1:56979887 | CAGCAACATGGGGGA[-/GG]GGTGGCGGGAGGGGG | 212712 |
rs211872293 | in-del | -/CT | | | intron-variant | Satb2 | Mm_Celera | 1:56837365 | CCAGCACGTTGCATA[-/CT]CTTTCACTGTGTGAT | 212712 |
rs211889361 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56919264 | GTCAACAGAGCAAAT[C/G]AAACAGGTCAGACAG | 212712 |
rs211894335 | in-del | -/ACAC | | | intron-variant | Satb2 | Mm_Celera | 1:56937981 | CCAAAACATATTCAT[-/ACAC]ACACACACACACACA | 212712 |
rs211911046 | in-del | -/ACACACACACACACACAC | | | intron-variant | Satb2 | Mm_Celera | 1:56889298 | TCTCTGAAAGAGCAA[-/ACACACACACACACACAC]ACACACACACACACA | 212712 |
rs211926201 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56885863 | GCTTTGTATATATTA[C/T]AAACTTTTAGAAACC | 212712 |
rs211948545 | snp | A/T | | | nc-transcript-variant, intron-variant, upstream-variant-2KB | 9130024F11Rik, Satb2 | Mm_Celera | 1:56975193 | TATATTTGATGATGA[A/T]TCAAAAAACTGTTTG | 212712 |
rs211949992 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56859677 | CAATTCCAGAACTTG[G/T]GAGGTTAAAAACAGG | 212712 |
rs211984704 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56816308 | TTCTCCTCTGGCCAT[C/T]TCCCCAATTTTTATT | 212712 |
rs211986185 | snp | A/G | | | intron-variant | Satb2 | GRCm38.p3 | 1:56911431 | AAGTGGCATGATTAT[A/G]AGGTGTCTGTGTCAC | 212712 |
rs212001077 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56870114 | TAGAAGAAAAAAAAA[A/G]TCAAACAAGCCACAC | 212712 |
rs212017917 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56927909 | AGAGAATCCCAGTTT[G/T]GGGGAGTTTTGTTGT | 212712 |
rs212035073 | in-del | -/A | | | intron-variant | Satb2 | Mm_Celera | 1:56852259 | ATCCTAATACCTGGG[-/A]TAAGTGCCTACACAA | 212712 |
rs212040348 | snp | A/T | | | downstream-variant-500B | Satb2 | Mm_Celera | 1:56793853 | ACTGAACAGAACTGA[A/T]ACATCTGTAACTGCG | 212712 |
rs212077014 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56926190 | GCCTCCTTGCCTTGG[C/T]CACCCCGACAGACTT | 212712 |
rs212080221 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56935475 | ATCAGAGTTAGAAGA[A/G]ACAGAGAGGCAAATC | 212712 |
rs212098765 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56903532 | GCTTGCTTTTTTTTT[C/T]CCTCTTTTTTTAATT | 212712 |
rs212099939 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56857397 | ACCTACAGCTGTACT[A/G]TGATTCTGGGTGTTG | 212712 |
rs212103936 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56916408 | AATAATTTGCCTATG[A/G]ATTGATTTTTCACTG | 212712 |
rs212126089 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56847610 | GCCACCAGGGAGAAG[A/G]AGTAAAGGACCATTC | 212712 |
rs212133252 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56868515 | GAAGGCCTGAGATTC[C/G]TTCAGGAGCAGGAAT | 212712 |
rs212141022 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56858591 | TCAAACCACACTAGC[A/G]CCAAAAAGCAAAAGC | 212712 |
rs212187028 | snp | C/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56901482 | AGGCAGAGGCCTCAG[C/T]GTGTGGCCCTTCATC | 212712 |
rs212194272 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56933877 | AAAACACCTTATTTC[C/T]GAGTAGGAAGTTTAT | 212712 |
rs212248943 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56927257 | CCAAGGAATATTAAA[A/G]GGTTGTTTAAATTCA | 212712 |
rs212259107 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56805255 | TGCTTGGGTGCCTCC[A/T]GCGTGCAATGCTAAG | 212712 |
rs212277794 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56802717 | AGTTCACTGGGCAGT[G/T]TTTGCATTTATATAT | 212712 |
rs212310680 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56959960 | GGTAAAAGAACCTTT[A/G]CTGACAAAGGTTTAA | 212712 |
rs212323889 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | Satb2, 9130024F11Rik | Mm_Celera | 1:56972047 | ATCAATCAATCGCTG[G/T]GAGCACGGCGACCCA | 212712 |
rs212352530 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56856816 | AAACAAACAAACAAA[C/T]AAAACCCCAAAACCA | 212712 |
rs212378315 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56949392 | CTGACTGAGGATAGA[G/T]AGGCCCAAGGCACAG | 212712 |
rs212391489 | in-del | -/GG | | | intron-variant | Satb2 | Mm_Celera | 1:56844861 | AGAGAGTGGGGGGTT[-/GG]GGGGGGGAGGGTCCC | 212712 |
rs212400926 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56848705 | AACAATTTGGCAGGA[C/T]GTGACAGAAGGTGAT | 212712 |
rs212407189 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56908084 | ACTGACCATGTAGTC[C/T]AGGATGACCTTGAAG | 212712 |
rs212411930 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56867830 | CTCGCACAGAGCAGT[A/G]CAGTCGGATCTCCTG | 212712 |
rs212446909 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56907105 | GCCCTGATTATGGCA[G/T]CTGCTCCTCAAAACA | 212712 |
rs212482758 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56916824 | TCAGTACTAACACAT[A/G]ATCCCATCTCACGTC | 212712 |
rs212485756 | snp | A/T | | | intron-variant, upstream-variant-2KB | Satb2, 9130024F11Rik | Mm_Celera | 1:56970283 | AAAGGAGCGTACTTA[A/T]GGGCGAGAGGTCCCA | 212712 |
rs212508863 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56933448 | AGTACACAGACAAGC[C/T]CACTGATGGACTGCC | 212712 |
rs212543795 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56835039 | ATTTGCTGTCTCCTC[A/C]CTGGCTCCCTCTGCA | 212712 |
rs212557745 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56855596 | AAACAGAAAGAGAAA[C/T]GGAGAAGGGAGCAGG | 212712 |
rs212565371 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56959156 | GAACCTTGTCTGAAG[A/G]TGCCTTTTGACCTGA | 212712 |
rs212571528 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56826257 | CCCTGGAACTGGTGT[C/T]CTGGCCATTGTGAGC | 212712 |
rs212580580 | snp | C/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56844860 | GCAGAGAGTGGGGGG[C/T]TGGGGGGGAGGGTCC | 212712 |
rs212624683 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56843809 | TGAGTTAATGTGGGA[A/C]AGCGGGAGGCCTTGC | 212712 |
rs212632214 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56915226 | TGTGCTTCCACTCAC[A/G]AGGCTTTAAGAACTG | 212712 |
rs212643657 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56965522 | TTGAATGCAGCAAGT[A/G]TGCACTGCATAATGA | 212712 |
rs212644664 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56896445 | AGATTATAATGATAC[C/T]TTTAGAACAGTAAAG | 212712 |
rs212668588 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56924577 | CCAGTGAGCTGACAC[A/C]CTGCAGCTACAGCAG | 212712 |
rs212670630 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56914777 | ATGATGTATGCTCAA[A/G]TCAGTTTTAATTGAA | 212712 |
rs212676504 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56813867 | GAAACTCCTGTAAGG[A/G]ACCCTAGACAGTCCC | 212712 |
rs212716308 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56801566 | ACAAGACAAAATGAA[C/T]GTCTCTAAAAGTGAT | 212712 |
rs212716970 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56824878 | AGGGAGGATGAGAGG[A/G]GAGGAAGGAGGAGAG | 212712 |
rs212735788 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56948287 | AGACAGCAGAACGGG[C/G]TGTTACAAGGCAGTT | 212712 |
rs212752940 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56940651 | ATGGATGACCTGAAC[A/T]TCTGAACATTTCAAC | 212712 |
rs212753306 | in-del | -/CCTG | | | intron-variant | Satb2 | Mm_Celera | 1:56905739 | TAGAATGCATTTAAT[-/CCTG]CCTGTATTTATAACA | 212712 |
rs212771009 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56941507 | ATTCTCCCTCAAAAG[A/G]TGTGAATTTCTGAAC | 212712 |
rs212797635 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56947464 | CATCTTTGGCATAGC[A/C]GAACAATAGAGTATG | 212712 |
rs212798016 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56884193 | TCTCGACTAATTATT[C/T]TCTCTGTCCTTAGTT | 212712 |
rs212798047 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56875035 | ATTCCCAGGTCTTTT[A/T]AAATGCTTATAGACA | 212712 |
rs212824607 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56966472 | CCCAGCCTTCATATG[G/T]TTTTTAAAGAGATAT | 212712 |
rs212835237 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56883229 | TTCCAGAAGAATTGG[A/C]AATTATTAACTCTTT | 212712 |
rs212875545 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56956491 | CTATTTGCTTCATTA[G/T]CTCAGGTTTTGAGCT | 212712 |
rs212878454 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56938837 | GTAAAACCAGTCCCC[C/T]TGAAGTGATGTCTCT | 212712 |
rs212900549 | in-del | -/AAAAAAA | | | intron-variant | Satb2 | Mm_Celera | 1:56929881 | CTTGTCTCAAAAATC[-/AAAAAAA]AAAACAAAACAAAAC | 212712 |
rs212916420 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56904783 | TGAAAGTTCTCAAAG[A/G]TCAGTGACATGGAGG | 212712 |
rs212934864 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56809636 | CAAGATACTATGGGA[C/T]GACTGTGTATGCTTT | 212712 |
rs212954456 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56945872 | GAACGGATAACCCTG[C/T]TTCTCCATCTACCCT | 212712 |
rs212990186 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56880339 | ATCTCAGATCCTCAA[C/G]TTTGGCGGAAAGTGC | 212712 |
rs212991894 | in-del | -/TTT | | | intron-variant | Satb2 | Mm_Celera | 1:56939837 | GGTTTTAAAAAGACA[-/TTT]TAAGATTATAAAATC | 212712 |
rs212992892 | snp | A/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56946590 | TCAAAGTTTACAGGG[A/T]CTGGGCAACAGTTCT | 212712 |
rs212996999 | in-del | -/GTC | | | intron-variant | Satb2 | Mm_Celera | 1:56898168 | GCTTCTGTGTCCTCT[-/GTC]AGTGTCTCATCTAGA | 212712 |
rs213016218 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56890998 | TACTTATTTACAACC[C/T]TTCCTAAATTAAGGG | 212712 |
rs213019190 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56954952 | CCTCCATACCAGCAT[C/T]TCTTCCTGGCTGTTG | 212712 |
rs213031074 | in-del | -/TTTG | | | intron-variant | Satb2 | Mm_Celera | 1:56921266 | TTTGGTATTGGTAGT[-/TTTG]TGTGTGTGTGTGTGT | 212712 |
rs213049367 | snp | A/G | | | intron-variant | Satb2 | GRCm38.p3 | 1:56924884 | ACTGCAGCAAGTCTG[A/G]ATTTAATTACAAGTC | 212712 |
rs213061972 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56821952 | ACTGAATATGTACAG[C/T]TTAGAAGAACATCTG | 212712 |
rs213067239 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56865985 | TACCCTTATCCAAaa[A/G]taaataaataaataa | 212712 |
rs213107050 | in-del | -/ACC | | | cds-indel, intron-variant | 9130024F11Rik, Satb2 | Mm_Celera | 1:56974207 | TACTAACTGTATTAA[-/ACC]CCCCCCTCCCACCCC | 212712 |
rs213114187 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56924341 | TCACTTCATTCAGTT[A/G]GAAATCCCACTCTAT | 212712 |
rs213117998 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56812469 | ATCAAAGGCGGGGCT[A/G]CTTTTCAGCCTTCAT | 212712 |
rs213179038 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56864790 | AATGGTATACGGCTC[G/T]GCAATCTAAGGTAAT | 212712 |
rs213182227 | in-del | -/GCCTGTGTAGGATAT | | | intron-variant | Satb2 | Mm_Celera | 1:56811999 | TACTGTGTGTCTGAG[-/GCCTGTGTAGGATAT]GGAATGGGCCACATT | 212712 |
rs213207562 | snp | C/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56932273 | TATGGGTCAAGGCCT[C/T]AGTAAAGTGCTTTAC | 212712 |
rs213220622 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56873789 | TAACAACTTAACATG[A/G]CTTCTTAAAAGAATA | 212712 |
rs213249295 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56873403 | GTGCACTTAGAAATC[A/G]GAGGCAGCACACCCC | 212712 |
rs213249356 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56881142 | TGGCTGGGTGAGTTA[C/T]GTAAGTAACAAGGGT | 212712 |
rs213249751 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56894632 | TAAAAAAAAAAAAAA[A/C]CCTATAGCACACACA | 212712 |
rs213254181 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56799796 | CTGTGAAGTCAAGTG[C/T]GGAGTTGAGATCCAC | 212712 |
rs213262172 | in-del | -/A | | | intron-variant | Satb2 | Mm_Celera | 1:56895543 | CAACTGTTTGCAGAC[-/A]AAAATAAGAAACAAG | 212712 |
rs213263534 | in-del | -/A | | | intron-variant | Satb2 | Mm_Celera | 1:56927441 | TGAAAGTGGTATTCC[-/A]AAATGCATGTTCAAT | 212712 |
rs213268492 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56930748 | AAGTATTATTAGCTT[C/T]CAGATGATGATTCTA | 212712 |
rs213291685 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56811054 | AAATTCCATCCTCCC[C/G]TTCATCAGCCTCATC | 212712 |
rs213294856 | snp | C/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56917002 | TGTTAGAATTTAACA[C/T]GTATTATCTTCTGTC | 212712 |
rs213299513 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56824073 | TAGTAACCTGGTTAG[A/C]GAATTTGCAAACATC | 212712 |
rs213316623 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56920921 | CTTAGGGTCACAGAT[A/G]TCTCTACACACAACA | 212712 |
rs213320125 | in-del | -/T | | | intron-variant | Satb2 | Mm_Celera | 1:56963558 | CCACCGCCCCCCCCC[-/T]TTTTTTTTTCAAAAA | 212712 |
rs213334456 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56851753 | GAAATTAATATAAGT[A/G]CAGGAGATGCAGCTC | 212712 |
rs213359065 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56822666 | CGAAAAGAAACATGG[A/C]GACGATGCCAGGAAA | 212712 |
rs213382035 | snp | A/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56915764 | CAAAGATAGAGAAGA[A/T]AAGTAAGTGTATTCT | 212712 |
rs213389678 | in-del | -/A | | | intron-variant | Satb2 | Mm_Celera | 1:56811344 | CCTGCACTTTCAAAG[-/A]AAAAAAAAAGGCCTA | 212712 |
rs213395432 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56862024 | ATGAGGACATGTCAA[C/T]CAAATGAGACCTCAC | 212712 |
rs213432701 | snp | C/T | | | synonymous-codon | Satb2 | Mm_Celera | 1:56796975 | CTTGCCATGGTGCTT[C/T]ACGTGGTACCTCTGG | 212712 |
rs213442803 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56870886 | GGTGTACATGCTTGT[A/G]GAGGCAAGACCTTGA | 212712 |
rs213449351 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56878557 | GAACCTCTGTCATTC[C/T]TGTGTGTTCATAACT | 212712 |
rs213467979 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56806853 | GTCCTGTACTTGAGG[C/T]TTCAACAACTTAGTG | 212712 |
rs213486170 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56928493 | CTCTGAGTCCTAAAG[C/G]CCCCTCGGTATATCA | 212712 |
rs213489958 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56913012 | ACTATTTCATATAAC[G/T]TTGGGTGACACATCA | 212712 |
rs213528707 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56832019 | CCGGAGCTCTTGACT[C/T]TAGCTGCATATGTAT | 212712 |
rs213545949 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56953954 | AAGCCCAAGAAAGAC[A/G]GGAGAAATTCAGGAA | 212712 |
rs213584383 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56852638 | TGAATCGATTCTCCC[A/G]AAATTAAGAGTCACT | 212712 |
rs213588722 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56855016 | ATTATAGTGATTGAC[C/T]TTCAAGCTTCCATGC | 212712 |
rs213597979 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56963169 | AAGCCCTCAACTGAC[C/T]TGTCTTAGCTCAGCC | 212712 |
rs213603237 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56911813 | TTAGAGAGAATGAGC[G/T]ATCACAGAGCTCTAC | 212712 |
rs213641966 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56922323 | AAAATTGAAAAGGTG[A/G]CAGAAAATGATTTCA | 212712 |
rs213667296 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56901150 | CCAGAGAATTCACTG[A/G]GAAGGGCTTGCTTGC | 212712 |
rs213702047 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56931484 | ACGTAACGATGTGAC[A/G]TAGAACTGTTCTTCC | 212712 |
rs213707128 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56839180 | CACCACTCATCAGGT[C/T]CTCTTCTTGAAACAA | 212712 |
rs213744069 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56850615 | GCTGTAATAATCCTA[C/T]GTGCGCCAATGCCAG | 212712 |
rs213775299 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56929245 | GAAGGAAAGACCACT[C/T]CACAGGCAATAGTCA | 212712 |
rs213778782 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56977903 | CATCCCGGGACTCTG[G/T]CCTCTTCATGCACGG | 212712 |
rs213781884 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56849848 | CCCCCAGAAAAATAA[A/G]CAAGCAATGTAAGGA | 212712 |
rs213787373 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56909509 | GTGTACCATTCTGAG[A/C]CCCGTTTTCTTTACT | 212712 |
rs213810895 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56919018 | AATGTCACAATGGAG[A/G]TGTGTACTGTTAAAT | 212712 |
rs213811317 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56863247 | TCATACTACTTTCCA[C/G]TCAGTGAACTGAAGA | 212712 |
rs213815306 | in-del | -/TATT | | | intron-variant | Satb2 | Mm_Celera | 1:56925147 | TTCAGCTGTTAAGAC[-/TATT]TAAGTGATTTTTTTT | 212712 |
rs213842824 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56927841 | AGACACAAACACATG[A/G]TGGCCAATGCTGCTA | 212712 |
rs213843143 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56917871 | GTGAAGCAGGGTAAA[C/T]GCCTGAGTTAGCAGC | 212712 |
rs213849444 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56872168 | GGATTAGCACAGCAT[A/G]AAGAATGGCATCAAA | 212712 |
rs213882550 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56960730 | AACATGAAAACGAGG[A/C]AGTTCAGGTTCTCGT | 212712 |
rs213889793 | in-del | -/G | | | intron-variant | Satb2 | Mm_Celera | 1:56826164 | GTATGAGTGTTATGT[-/G]CTTAAGTGTGTATGC | 212712 |
rs213891757 | in-del | -/CACA | | | intron-variant | Satb2 | Mm_Celera | 1:56951020 | GCACGCACACTCAAG[-/CACA]CACACACACACACAG | 212712 |
rs213905159 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56952868 | GGAAGTACGTGATCG[A/T]CCTGAGCACTTCACC | 212712 |
rs213906704 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56944269 | GACAACAAAGACAAC[C/T]GGTTTGGGGGGGGGC | 212712 |
rs213923772 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56819528 | TCTTACTTTGACTTT[G/T]GGAGGACTTTAAGAC | 212712 |
rs213933290 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56937850 | AAACCAAAACTAAAT[A/G]AACTGATACAATAGG | 212712 |
rs213941380 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56944510 | GTGGTGGATGTACGT[A/T]TGTGCAGGCAAGACA | 212712 |
rs213948653 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56877793 | ATATAATTATATTAT[A/G]AAGAAACATTGATTG | 212712 |
rs213962332 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56951351 | CCCAGGGAAGCCTAC[A/G]CAGGGCAAGAAGAAA | 212712 |
rs213975413 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56889094 | CTACTGACACACACA[C/G]ACAGAGATACACACA | 212712 |
rs214006604 | in-del | -/TTTC | | | intron-variant | Satb2 | Mm_Celera | 1:56882742 | TATTTATATTCATAT[-/TTTC]TCTCTCTCTCTCTCT | 212712 |
rs214019829 | snp | A/T | | | upstream-variant-2KB | Satb2 | Mm_Celera | 1:56979450 | TTACCTGAAGTTAAA[A/T]TCTGTTTCAAAGGCA | 212712 |
rs214063194 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56964041 | GTGAGTTATATGTTT[C/T]CTGCTATGAAGAACA | 212712 |
rs214113393 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56950487 | CTAAGTAAGTCTGGG[A/G]CTGGTCCTATTAATT | 212712 |
rs214129645 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56885554 | GCTTCCATGGCCAGT[C/T]TGAGGCAACACGCAT | 212712 |
rs214137215 | snp | C/G | | | intron-variant | Satb2 | Mm_Celera | 1:56959106 | CTCCCTCAACAAAGG[C/G]CTCCTGATACCAATA | 212712 |
rs214159315 | in-del | -/T | | | intron-variant | Satb2 | Mm_Celera | 1:56881226 | GCTTGAAAAATTTAA[-/T]CAAAAAAAAAAAAAA | 212712 |
rs214162865 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56896382 | CAAGTGGCAGGCAGT[A/G]GGTGACCGTGTCTAC | 212712 |
rs214192103 | in-del | -/A | | | intron-variant | Satb2 | Mm_Celera | 1:56857888 | TACATTGGCCACTAT[-/A]AAAAACTGCCTCCTA | 212712 |
rs214197162 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56895455 | GAACCCTCTCACTGG[C/T]CCTCAGTTTCTTAAG | 212712 |
rs214221735 | in-del | -/A | | | intron-variant | Satb2 | Mm_Celera | 1:56954827 | AAAAAAAAAAAGTAG[-/A]AAAAAAATTCATCAA | 212712 |
rs214228187 | in-del | -/AAAAAAAAAA | | | intron-variant | Satb2 | Mm_Celera | 1:56854097 | CCTGGGCTCTGGAAG[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 212712 |
rs214240898 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56927176 | CAATCACATTGTATA[C/T]AATCCCTTGTCCCCC | 212712 |
rs214273856 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56858506 | TCCTCCTCACCCTTC[A/G]CTCCGTCTTGTCGTT | 212712 |
rs214281140 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56898617 | CAAAAAGAAAGACAT[C/T]TCTAAACAAAACCGT | 212712 |
rs214288244 | in-del | -/G | | | intron-variant | Satb2 | Mm_Celera | 1:56948468 | CAGCAGCATTGCTGA[-/G]GACTGGGGCAAAAGA | 212712 |
rs214316179 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56838602 | TTGGGGGGGTGGGGT[A/T]GTATATGACACAGTC | 212712 |
rs214317693 | snp | C/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56961708 | TTCCAGCTATGGACC[C/T]AAATCAAGCAAAGAC | 212712 |
rs214341612 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56876966 | GTCCACTTTTAATTG[A/G]CAGAGGGACATCAAC | 212712 |
rs214358717 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56859215 | ACTGGACTGGAATTA[G/T]ACACCGATCAATCAC | 212712 |
rs214369610 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56804564 | TCAAACACCCCAGAG[C/T]AGGATGATGAGTGAC | 212712 |
rs214378433 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56886613 | CCGATACCACGGTGG[C/T]GAAGCAAGGGGCGCC | 212712 |
rs214393129 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56908566 | AATAGGTGCTCATTC[A/C]GCAGACAAATGTTTC | 212712 |
rs214396881 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56826115 | TTGTTTCCCTTGTCA[G/T]GTGCCCTGCCCTCTA | 212712 |
rs214398893 | in-del | -/AAAAG | | | intron-variant | Satb2 | Mm_Celera | 1:56819748 | ACTGAGGCCAATCAC[-/AAAAG]AAGTCACTTGATATG | 212712 |
rs214400415 | in-del | -/T | | | intron-variant | Satb2 | Mm_Celera | 1:56817781 | AGTTCTGTATTGGTG[-/T]TTTAAAAAAAAAGAT | 212712 |
rs214408931 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56803713 | GGCATTGATTAAAGG[A/T]ATGAAAATATGTCTG | 212712 |
rs214422983 | snp | A/G | | | intron-variant | Satb2 | GRCm38.p3 | 1:56944809 | GCAAGTTTAAGATGA[A/G]GGGAAGGGGACTCTG | 212712 |
rs214441092 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56933253 | TAGAAGAAAAAGGAG[C/T]TAACAAGTCACGTGG | 212712 |
rs214442614 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56924695 | ACACCACCTTCAAGA[A/C]ATACCAAGTCCCTCT | 212712 |
rs214452928 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant, intron-variant | Satb2, 9130024F11Rik | Mm_Celera | 1:56972660 | TTCTCCCTCAAATCC[C/G]GTGCGGCCGCGGGTC | 212712 |
rs214466490 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56856001 | CGTTAGTAAGATCTG[G/T]AGGTGCTGGTGTGCA | 212712 |
rs214471130 | in-del | -/A | | | intron-variant | Satb2 | Mm_Celera | 1:56872770 | TTATTGCAAATTATT[-/A]AAGGTTTAAAGGATA | 212712 |
rs214478107 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56932653 | CTAACAGACCTGCAG[G/T]GCCCACTGTCCTAGG | 212712 |
rs214492391 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56820927 | ATATGGCAGAGCTGG[A/G]GATCCATGGGCTAGT | 212712 |
rs214520826 | snp | A/G | | | intron-variant | Satb2 | GRCm38.p3 | 1:56906938 | CACAAACAAGAACTC[A/G]CCACTTCTTTTCTCC | 212712 |
rs214535653 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56829867 | AGGGTGGCAGGTGAT[A/G]AGGAGTTTCCTAGAG | 212712 |
rs214565133 | in-del | -/A | | | intron-variant | Satb2 | Mm_Celera | 1:56896100 | GCATGATTTATTAAG[-/A]AAAATGCAGAAAGAC | 212712 |
rs214581682 | in-del | -/TTGT | | | intron-variant | Satb2 | Mm_Celera | 1:56935944 | TTTATGATACAATGC[-/TTGT]TTAACACTCCTTTTG | 212712 |
rs214596923 | in-del | -/C | | | intron-variant | Satb2 | Mm_Celera | 1:56921376 | TCAGGAAAAAAAAAA[-/C]AAACTGTTTCCTGAA | 212712 |
rs214614531 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56899383 | TTACTTAGAAAACCA[C/T]ACTGATATTTCCTTT | 212712 |
rs214626332 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56934681 | ACTGGGTTGGATCCT[A/G]GCTCCATTGCTTATT | 212712 |
rs214648169 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56848509 | TCCAATAATGGCTAA[A/C]CGTTGTAAAAGTACT | 212712 |
rs214655536 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56869484 | CCTGCCTCTGCCTCC[C/T]GAGTGCTGGGATTAA | 212712 |
rs214655888 | in-del | -/AAAT | | | intron-variant | Satb2 | Mm_Celera | 1:56923083 | AACAAACAAACAAAC[-/AAAT]AACATAGAGATCAGA | 212712 |
rs214683092 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56847466 | TTCCCACTCTACCAC[G/T]CAGTCATGTGAACTC | 212712 |
rs214690398 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56957838 | CTCCAAGCAAAGAAT[G/T]TTAAACTGGGGATAA | 212712 |
rs214693461 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56943011 | GAGATTTATTAACAC[A/G]TAGGCCAGAATTGTT | 212712 |
rs214722365 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56856631 | ATACATTTCACAGGG[C/T]ATTTAATGGCAAACC | 212712 |
rs214786582 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56942421 | GGAAGACCCTGAAAA[C/T]GTGGTAAGGAACTGA | 212712 |
rs214805484 | snp | A/C/G | | | intron-variant | Satb2 | GRCm38.p3 | 1:56925333 | ATGATATTTAAGGCT[A/C/G]CTAGAAGGAACTGCT | 212712 |
rs214871024 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56965224 | GTTCTCTCCACTTCC[C/T]TGGGTTGACAATGAT | 212712 |
rs214874036 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56875842 | TCTTCTCCCACCATC[A/G]ACCAAGGATGCATGC | 212712 |
rs214885862 | snp | A/C/T | | | intron-variant | Satb2 | GRCm38.p3 | 1:56940609 | GACTGTCATGTATAC[A/C/T]GGGCTGGCCTTGATC | 212712 |
rs214904767 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56854928 | ATTTCAGTTTCAATC[A/C]GTTTCAAGTGATACA | 212712 |
rs214931133 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56825381 | AATTTTAAAACAAGT[A/T]CTTCTCAAGAAACCA | 212712 |
rs214935431 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56907810 | GCCAGGGCCAAAAAG[C/T]GGGAGTGGGTGGGTA | 212712 |
rs214939141 | snp | A/T | | | intron-variant | Satb2 | Mm_Celera | 1:56854270 | GTAGGGTACAGAACA[A/T]TTTCCAGGGAGACAT | 212712 |
rs214940439 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56865744 | TCAAAGGTGGCAATG[C/T]CAAAAAAAAAATCTT | 212712 |
rs214954556 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56924273 | TAACGGAAGAAATGG[C/T]CCTCAATTGTGTTAT | 212712 |
rs214990505 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56923354 | AAATTTGTAGATTTT[A/G]CAATCATATTGGATG | 212712 |
rs214990823 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56931366 | CATTTGAGAAAAGGT[A/G]TGCACAGCTTAAATG | 212712 |
rs214999276 | in-del | -/GAGAGA | | | intron-variant | Satb2 | Mm_Celera | 1:56931772 | TTTTTGGTATAAAGT[-/GAGAGA]GAGAGAGAGAGATAA | 212712 |
rs214999761 | in-del | -/GGATGGAT | | | intron-variant | Satb2 | Mm_Celera | 1:56885911 | GATTGTAACTATCCA[-/GGATGGAT]GGATGGATGGATAGA | 212712 |
rs215030235 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56823986 | CACAGCAAGGGCTGA[A/G]AACGGAAACTACATT | 212712 |
rs215030827 | snp | A/G | | | intron-variant | Satb2 | Mm_Celera | 1:56798500 | TGTGTAGCAGAGGAT[A/G]GCCTTATCTGGCATC | 212712 |
rs215033292 | in-del | -/T | | | intron-variant | Satb2 | Mm_Celera | 1:56894080 | ATCCAGCACATGCAC[-/T]TCTGCTTCTATGGAA | 212712 |
rs215047544 | snp | G/T | | | intron-variant | Satb2 | Mm_Celera | 1:56956323 | GAGCAATTTGATTCT[G/T]CAAGTTTCTGACAGG | 212712 |
rs215066637 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56823330 | TACAGTGTGGAGACG[C/T]ACAGGCCATGAGGGC | 212712 |
rs215079423 | in-del | -/T | | | upstream-variant-2KB | Satb2 | Mm_Celera | 1:56980478 | AATCCACTTTTATTC[-/T]TTTTTCTGGTTTTGC | 212712 |
rs215089900 | snp | A/T | | | intron-variant, upstream-variant-2KB | Satb2, 9130024F11Rik | Mm_Celera | 1:56970125 | GTCTCAGGTCCCAAG[A/T]GTTAGCCCTCAGTTG | 212712 |
rs215099869 | in-del | -/ACACACACACACAC | | | intron-variant | Satb2 | GRCm38.p3 | 1:56965773 | AAACTAGAACATTTA[-/ACACACACACACAC]ACACACACACACACA | 212712 |
rs215105082 | snp | C/T | | | intron-variant | Satb2 | Mm_Celera | 1:56894407 | CACTACTATATATCA[C/T]TCTCCTTACTGTATT | 212712 |
rs215133812 | snp | A/C | | | intron-variant | Satb2 | GRCm38.p3 | 1:56808656 | TTCAACCAGAAGCAC[A/C]TATTACATCAAGCAC | 212712 |
rs215140396 | snp | A/C | | | intron-variant | Satb2 | Mm_Celera | 1:56893772 | CATCTTAACTCTCTG[A/C]ACAGAGTACACTCAG | 212712 |