| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs13451031 | snp | C/T | 0.276506 | 0.248591 | intron-variant | Satb2 | Rn_Celera | 9:63510676 | TCAAACTATGTGCCT[C/T]GCCACTGCACAGTCC | 501145 |
| rs13451032 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63511000 | CAATACACACTGTGA[C/T]GCCAGGGAGAGTGAG | 501145 |
| rs64574095 | snp | A/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63577680 | CCATGACAATAATGG[A/T]TTAAACCTCTGACCC | 501145 |
| rs64819970 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | Satb2, LOC102549320 | Rn_Celera | 9:63642225 | TTGTTTGTTTTGTTT[G/T]GTTTTTTTCTCTCCA | 501145 |
| rs65118687 | snp | C/T | 0.47947 | 0.099214 | intron-variant | Satb2 | Rn_Celera | 9:63577882 | CAAAATTGGTAACAG[C/T]TATTAGGACAAGAAT | 501145 |
| rs65464525 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63576816 | CTTTAAAGTCATTTC[C/T]TTGGGTAGTTTTGTC | 501145 |
| rs66226053 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | Satb2, LOC102549320 | Rn_Celera | 9:63642226 | TGTTTGTTTTGTTTT[G/T]TTTTTTTCTCTCCAC | 501145 |
| rs66360544 | snp | A/C | 0.499657 | 0.0130845 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Satb2, LOC102549320 | Rn_Celera | 9:63642134 | CCAGCCTCTCTGGCT[A/C]TCAAGTTCGGTGACC | 501145 |
| rs104897544 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63535926 | TGTGCTGGCACAGAG[A/G]AAGGAGATCACTCTT | 501145 |
| rs104898652 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63587634 | AGGGGAAAGCTTGCT[A/G]GGTAAAATACTTCAT | 501145 |
| rs104922915 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63526261 | GTCAGCAGCATGCCA[C/T]AGCTGAGAAGACTGA | 501145 |
| rs104932120 | snp | G/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63587515 | CCAAACCCCACAGGC[G/T]CATTTCTAGAAAGTA | 501145 |
| rs104955096 | snp | A/C | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63569325 | TCATGTGACTCTAGA[A/C]AGTTACTTAATGTCT | 501145 |
| rs104962542 | snp | C/T | 0.375 | 0.216506 | intron-variant | Satb2 | Rn_Celera | 9:63616592 | ACCTTTTAACTCTTA[C/T]ATACTGGTATATGAT | 501145 |
| rs104983534 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63569415 | AGAGTGTGTGAGTTA[C/T]AGGTAAGGTCCTTCG | 501145 |
| rs104987326 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63513743 | GCGAGCAAGGTAGGC[A/G]CTCAGGAGGAAATGT | 501145 |
| rs105034413 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63514338 | ACTCCAGTAAAGCAA[C/T]ATGGCCTCAGGGGAC | 501145 |
| rs105073223 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63488255 | GCCTGCTAGGCAAGC[A/G]CCCTACCACTGAGCT | 501145 |
| rs105105115 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63508120 | TGCTTCATCTAACTT[C/T]CATTTCCTCTGTCCT | 501145 |
| rs105110498 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63507986 | AACTACAGCACACAG[C/T]ACACATCTGTCAGGG | 501145 |
| rs105134920 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63622824 | ATTTACGAGGACACA[C/T]GTTTGTCTTGCTCCC | 501145 |
| rs105163798 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63617343 | CACCCGCTATGCATG[C/T]ACGCGCACACACACG | 501145 |
| rs105165973 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63575638 | TGCTCGCCACTGTGA[A/G]CCTGCGAATCTGATG | 501145 |
| rs105198397 | snp | C/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63628776 | TGCACTGCTCTGATA[C/G]CTATAATATCTACTC | 501145 |
| rs105228683 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63465168 | GTGTGTGTGCGCGTG[C/T]GTGTGTGTTTTCAAG | 501145 |
| rs105259622 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63530845 | CCTAGGACAGAATGA[C/T]TTTAGGTATAGACAT | 501145 |
| rs105265954 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63538694 | ACCCTAGAAAGTCAT[A/G]GCCAGGAGCCTTCCA | 501145 |
| rs105281539 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63463664 | CCACAACACAAATGC[A/G]CAAAGAGGACAAATG | 501145 |
| rs105302663 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63621558 | ACACATGCACACACA[C/T]ACACACACACACACA | 501145 |
| rs105372198 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63590658 | GGGGCGTGCGTGCTC[A/G]CGTGTGTATTCAGCT | 501145 |
| rs105404139 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63511611 | TAATCCTCAAAAGTG[C/T]TTGAATATTTCATAT | 501145 |
| rs105414721 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63517627 | GGGGTGATTTTAAAG[C/T]AGAAGAAGTCATGTT | 501145 |
| rs105416367 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63578300 | ATAGTCTGGTGAGCT[A/G]AATGGGAGTGTGTAT | 501145 |
| rs105426376 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63618929 | GTATAAAATACACTC[A/G]ATTTTAATGATTTAC | 501145 |
| rs105428995 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63507663 | AGGAAGGAAGTCAGA[A/G]TCATTTTCAAGAATG | 501145 |
| rs105450068 | snp | A/G | 0.375 | 0.216506 | intron-variant | Satb2 | Rn_Celera | 9:63617887 | ACAGCTACAAGTGTT[A/G]CGGTCACAGAGAAAG | 501145 |
| rs105455940 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63476091 | TAGGGCAAAGAAACT[A/G]GACGGGAGGTTCCTT | 501145 |
| rs105483667 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63575829 | ATTAGAAACTTTTCA[C/T]CAAATGTGAACTGTA | 501145 |
| rs105493747 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63538831 | TACAACCATGGGGCT[A/G]CAGCAACTTAAGGAC | 501145 |
| rs105495759 | snp | C/T | 0.375 | 0.216506 | intron-variant | Satb2 | Rn_Celera | 9:63570241 | TTCTAGAATCGTATA[C/T]GCGCTCAGATTCCAA | 501145 |
| rs105552302 | snp | C/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63524523 | GGACCATGGAGTCAA[C/G]ACCCTAGGTTTACAT | 501145 |
| rs105579116 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63630834 | GATGAGGAGAAGGAG[A/G]AGGAGGAGGAGGAGG | 501145 |
| rs105582632 | snp | A/G | 0.375 | 0.216506 | intron-variant | Satb2 | Rn_Celera | 9:63614271 | CTAAGCACTGAGCCC[A/G]AAAACACCAATTTGC | 501145 |
| rs105597844 | snp | A/C | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63463790 | CAGTGTAGTCTGGAC[A/C]AAGAGGTAACTGGGA | 501145 |
| rs105622018 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63529011 | CTTTAATCCATAAAG[A/G]AAGACATAAAGGATT | 501145 |
| rs105647614 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63511456 | TTTATCACTGAGATG[C/T]GTTAGAATGAACTTT | 501145 |
| rs105652414 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63508671 | AAGCTTTGGATAAGG[A/G]AAAAATATTTTAACT | 501145 |
| rs105655363 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63579993 | GCTTCACCCATGAGC[A/G]TCAACAATGGCTGCC | 501145 |
| rs105659428 | snp | A/C | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63508944 | CAAAACAAAACAAAA[A/C]ACCCCTACTCACCTG | 501145 |
| rs105672203 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63579754 | CTGATCATGGATAAC[C/T]TGCAAAACTAGTTAC | 501145 |
| rs105677620 | snp | C/T | 0.5 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63558208 | AAATACTTATGTGTA[C/T]ACACACACACACACA | 501145 |
| rs105696881 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63467369 | TTGGACACCTCCTGT[A/G]TACAACACTAAGACG | 501145 |
| rs105703580 | snp | A/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63542448 | CTTTGTTGTGTTGGG[A/T]CCCCCTCCCCCACCT | 501145 |
| rs105722336 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63537910 | AAATGCACATCAGTA[A/G]TCTATTGTGCTATGG | 501145 |
| rs105723930 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63464376 | CAATGAGCACAGTAC[A/G]TGGGGAAACAGGAAG | 501145 |
| rs105725734 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63464512 | CATTCTCTATTATCT[A/G]TCTGTTTGTCTGTCT | 501145 |
| rs105732626 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63546824 | TTACAGGCTCGCTCC[C/T]CTTTCTTCTAGTTAT | 501145 |
| rs105751525 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63624592 | GGTCAGGGCAAGAGC[A/G]AGCATTCTGTCTCTG | 501145 |
| rs105756398 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63561203 | ACCAGATGAGACGCA[A/G]AAGGCAGAATGGGAT | 501145 |
| rs105800361 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63539319 | ACATATATATGGAGA[A/G]GGAGAAGGGAGAGCA | 501145 |
| rs105801357 | snp | A/G | 0.375 | 0.216506 | intron-variant | Satb2 | Rn_Celera | 9:63468251 | ATGACAAAAGCCGAC[A/G]GAGAGAGATAAAGCC | 501145 |
| rs105812506 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63467324 | AAAACGGCCTTCAGT[C/T]CTTCAGCCTCTTAGC | 501145 |
| rs105839534 | snp | C/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63465119 | TCTCTCTCTCTCTGT[C/G]TGTGTGTGTGTGTGT | 501145 |
| rs105951855 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63526927 | CAGAAGTATAAGCAT[A/G]AGTGTGGAGCAGCTC | 501145 |
| rs105969778 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63562882 | GGAGGTTGACACTTC[C/T]GCTCATCCTTGTCTG | 501145 |
| rs106036619 | snp | A/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63596670 | TTTGAGCATGGTCCC[A/T]TTTGATTCCTGACCT | 501145 |
| rs106040199 | snp | G/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63539599 | TTTCAACACCTACAC[G/T]CATTTGCAGATGCGT | 501145 |
| rs106048947 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63540144 | TAATTTATTGGTGTC[A/G]TTTTATTTTTTAAGG | 501145 |
| rs106059938 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63606681 | AATAAAAATCAAACA[C/T]AGAATGAATCATACT | 501145 |
| rs106078809 | snp | G/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63540482 | TCAGAAGAAGGCATC[G/T]GATGCCATTACAGAT | 501145 |
| rs106094226 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63569258 | AGTATGAATGAGTGC[A/G]GGCTTCCAAGGAAAC | 501145 |
| rs106120912 | snp | C/T | 0.375 | 0.216506 | intron-variant | Satb2 | Rn_Celera | 9:63526226 | GGCAGGGCCAGGGAG[C/T]GAAGAGACTGTAAAC | 501145 |
| rs106122014 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63562072 | TGAGCTCATGCTCAT[A/G]TGCTGCCGTCCCACA | 501145 |
| rs106148284 | snp | C/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63512620 | TAGAAGTGTGGAGAC[C/G]GGGAGGCCAGACCTC | 501145 |
| rs106167464 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63621559 | CACATGCACACACAC[A/G]CACACACACACACAC | 501145 |
| rs106189676 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63517789 | CACTCATAAAGGGGC[A/G]GGACATGCTAGTGAC | 501145 |
| rs106250302 | snp | C/G | 0.5 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63633179 | AGCATTCACCACTTC[C/G]ACTAGTTCAAACCAG | 501145 |
| rs106259538 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63618491 | GGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 501145 |
| rs106269080 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63565249 | GCTAGAAAAGGAAAG[A/G]GATGGTCAGTCCCCA | 501145 |
| rs106269799 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63541272 | GTTTATAGGGCTGGT[A/G]AGAAGGCTGAGTGGG | 501145 |
| rs106284768 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63464540 | TCTGTCTGTCTGTCT[A/G]TCTGTCTGTCTGTCT | 501145 |
| rs106309892 | snp | G/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63514175 | CATTAGCTAGGGACC[G/T]AGACATGCTCTAACT | 501145 |
| rs106371879 | snp | C/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63542374 | ATATTCCAAATATGA[C/G]CTATTGGTTCTAACA | 501145 |
| rs106392007 | snp | A/G | 0.5 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63516554 | CGAACAAGCTTGGCT[A/G]GTAGCACCTTCACAT | 501145 |
| rs106423137 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63617016 | TGTGACTGAGGGGGG[C/T]GACCGTTGGCCAGCA | 501145 |
| rs106434093 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63546540 | ACTACTGAGCCTTAA[C/T]AAGGCCTGCTTCCCT | 501145 |
| rs106446231 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63532204 | CTGAGCCCATCATTA[C/T]GCTTCTCCCTGCACC | 501145 |
| rs106464865 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63541427 | ACTTTTAAAACAGTA[C/T]ATTTTATAGAAATGC | 501145 |
| rs106490295 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63566804 | TTTCACAAATGACAC[C/T]GGGTAACAAAACTTT | 501145 |
| rs106518872 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63610489 | ACTGGGAAAGGCAAC[A/G]CAGATGTAGCGGTTT | 501145 |
| rs106568931 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63511487 | AAAGACATAGGCACG[C/T]AGGGATGTATGAAAT | 501145 |
| rs106588295 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63462458 | CTCCCAAACCAGGGT[C/T]CCAGATTACACATTT | 501145 |
| rs106601874 | snp | A/G | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63541024 | AAATGAGCATTAACC[A/G]TTCCATGCTGAGCTG | 501145 |
| rs106602186 | snp | A/C | 0.5 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63538637 | GCACAGGGCCAAAGA[A/C]CTCTGTGTCTCCATG | 501145 |
| rs106612725 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63522631 | TTAAAAATAAGCTTT[C/T]ATCTATATCATCATT | 501145 |
| rs106645685 | snp | A/G | 0.375 | 0.216506 | intron-variant | Satb2 | Rn_Celera | 9:63575792 | TGGAAGGTAAAGAAC[A/G]ATTTCTTATATATGA | 501145 |
| rs106654800 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63464518 | CTATTATCTATCTGT[C/T]TGTCTGTCTGTCTGT | 501145 |
| rs106683221 | snp | A/C | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63542365 | ATACAGGGGATATTC[A/C]AAATATGACCTATTG | 501145 |
| rs106687196 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63531692 | CTCAGGAACCCAGAC[C/T]TAGGCTGGTCCTTGG | 501145 |
| rs106703983 | snp | C/T | 0 | 0 | intron-variant | Satb2 | Rn_Celera | 9:63610857 | ACAGTGTGATTAGCG[C/T]GCCCCTTCTGAAGCA | 501145 |