| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs6154350 | snp | C/T | 0.5 | 0 | intron-variant | Ep300 | Mm_Celera | 15:81612658 | gtgtgtgtgtgtgtg[C/T]gcgcgngngtgcgtg | 328572 |
| rs6154362 | snp | C/T | 0.5 | 0 | intron-variant | Ep300 | Mm_Celera | 15:81612664 | gtgtgtgtgngcgcg[C/T]gngtgcgtgtgcatg | 328572 |
| rs6154363 | snp | C/T | 0.5 | 0 | intron-variant | Ep300 | Mm_Celera | 15:81612666 | gtgtgtgngcgcgng[C/T]gtgcgtgtgcatgca | 328572 |
| rs6168681 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Ep300 | Mm_Celera | 15:81612991 | aaaccaaaaaTTTGC[A/T]TGTGCATATATAAAG | 328572 |
| rs6362097 | snp | C/G | 0.5 | 0 | intron-variant | Ep300 | Mm_Celera | 15:81603231 | ttcttagccctcgag[C/G]catctctctagcccT | 328572 |
| rs13459688 | snp | A/G | | | utr-variant-3-prime | Ep300 | Mm_Celera | 15:81651736 | AGCTGCCAAATTGAT[A/G]TATTATAATATTGTG | 328572 |
| rs31584946 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Ep300 | Mm_Celera | 15:81604716 | TAATTTTTAGAATTT[A/T]CTCTTGGCATCAATC | 328572 |
| rs31620317 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ep300 | Mm_Celera | 15:81622762 | GAGGTCAGCAACAAA[A/G]ACATGGCCAAAGTGC | 328572 |
| rs31897910 | snp | A/C | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81622484 | TATATATATACACAC[A/C]CACACACACATATAT | 328572 |
| rs31899562 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ep300 | Mm_Celera | 15:81647336 | GATGCATTTCAAGTT[C/T]ATGACTAGGATTTTA | 328572 |
| rs31917655 | snp | A/T | 0.5 | 0 | intron-variant | Ep300 | Mm_Celera | 15:81611916 | ATAGATGACAAATTT[A/T]AAAAAAATTTTTTTT | 328572 |
| rs32242613 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ep300 | Mm_Celera | 15:81588165 | AATTTTTTTTAAATT[A/G]TGTCTTTGAAATTCA | 328572 |
| rs33858657 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ep300 | Mm_Celera | 15:81602883 | TTTCATTTTTTATTG[G/T]TATTTGTATGTGATG | 328572 |
| rs33885551 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ep300 | Mm_Celera | 15:81627958 | TCTTCCTCCTCCTCC[C/T]CCTCCTCCTCCTCCT | 328572 |
| rs45779300 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81595938 | TATACTAGGGAAGTG[A/G]CTCAAACCTTGGACA | 328572 |
| rs45864429 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81619440 | TTAGAGAAGAGTAAA[A/G]CTGGGCATGCATTAT | 328572 |
| rs45870460 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81595909 | TTGTATGAACAGATG[A/G]AGGATCAAATGTATA | 328572 |
| rs45941958 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ep300 | Mm_Celera | 15:81643506 | TCTCTAGTTTATTTT[C/T]CCAGAAGTGCTGAGC | 328572 |
| rs45979282 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Ep300 | Mm_Celera | 15:81600936 | GTTTGACCTGGAACA[C/T]GACTTACCAGATGAA | 328572 |
| rs46138992 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81643938 | CCAGGACCTTTTAAG[C/G]CAAGCATGGCAGTGC | 328572 |
| rs46281269 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ep300 | Mm_Celera | 15:81619943 | ATTGTGTGGTTTTGT[C/T]TTGTGAATTTGGGTA | 328572 |
| rs46284545 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ep300 | Mm_Celera | 15:81620951 | CCTACCTTTGCCTCT[A/G]CAGCCAGCTTTAGCT | 328572 |
| rs46337614 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81609096 | CTGCATGAGTGGCTA[C/T]GGTTAAGCTTCATTA | 328572 |
| rs46356975 | snp | A/G | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81595421 | TAACACCTATGATGT[A/G]CCTTGGCTGAAATAG | 328572 |
| rs46367735 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ep300 | Mm_Celera | 15:81636752 | AATCTTAGAATTCAT[A/G]CTGTTCATTTCAGGT | 328572 |
| rs46400874 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ep300 | Mm_Celera | 15:81602858 | AGCTAGCTTTCTTGT[C/T]CTTGTATTTTTTCAT | 328572 |
| rs46468582 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Ep300 | Mm_Celera | 15:81638728 | GTTTTTGAGATGCTC[A/T]CACTGGCTCGCCAGG | 328572 |
| rs46518264 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81599237 | ATTAAAACAAGTCAG[C/T]AAGATGGTGATGTTT | 328572 |
| rs46536510 | snp | G/T | | | utr-variant-3-prime | Ep300 | Mm_Celera | 15:81651141 | GGTTTAAAGTAAACA[G/T]GCCAGATGAACCTGA | 328572 |
| rs46538466 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ep300 | Mm_Celera | 15:81645182 | ACTGAGATGAAGAGA[A/G]TATGCATATAGAGTT | 328572 |
| rs46572490 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Ep300 | Mm_Celera | 15:81610432 | GGGTTCTGGAGCACA[C/T]ACAGCTGATCCAGAG | 328572 |
| rs46650776 | snp | A/G | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81606218 | TTTCGATCTAGGATA[A/G]CAACACTGGTCCTTT | 328572 |
| rs46663411 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81634178 | GACTGTTGTCTGTCC[A/G]ATACTGTATCCCACC | 328572 |
| rs46711480 | snp | A/G | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81609275 | GCTAGGCATGGTGGA[A/G]CACAACTTTAATCTG | 328572 |
| rs46778828 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81641098 | GCATCTGCTTTTGGG[A/T]CTTATTGAGAGTAAA | 328572 |
| rs46796815 | snp | A/G | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81599200 | GAAAACCTTAAAGGA[A/G]AGAAAACTCAAACAC | 328572 |
| rs46838454 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Ep300 | Mm_Celera | 15:81638956 | TTTTATGTTATATAA[A/G]CAAAGTCCTGGTTTA | 328572 |
| rs46899488 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81603801 | TGTTAAAAATTTGTT[A/G]CTTAGCTGGGCAGTG | 328572 |
| rs46923210 | snp | C/G | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81608946 | GGAAGAAGAACCTTT[C/G]TGCGCTTGCAGGAGA | 328572 |
| rs46926107 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81601845 | CAATTTTAAGATAAC[A/G]GGTATTAACACTGTT | 328572 |
| rs47034704 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Ep300 | Mm_Celera | 15:81591764 | TAAAGTAATATATTG[G/T]GGTAAATTAAAAAAA | 328572 |
| rs47062972 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81638411 | TATTATAGAATTTAA[C/T]GCCAGTTCTTGATCC | 328572 |
| rs47178453 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81623660 | CAGCAAGTCTTGTAA[C/T]AGTCTGCTTTGGAAA | 328572 |
| rs47181768 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81599592 | TGCATCCAGACTTGT[A/G]TTGGTTGTATATGTA | 328572 |
| rs47235612 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ep300 | Mm_Celera | 15:81636500 | TCTGAGCCTCGTGCA[C/T]TCAAGAGGACATGTT | 328572 |
| rs47290393 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81602778 | GTCTCCTGGCTTTTA[C/T]AGGAGTTCTCTGTAT | 328572 |
| rs47373584 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ep300 | Mm_Celera | 15:81621423 | ATTGGCTTTCTCTAG[C/T]ATCTACTGTCTTATA | 328572 |
| rs47376683 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81596134 | TTAAAGGTATCTGAT[A/G]GGGGCCAGTCGGTGG | 328572 |
| rs47451470 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81636119 | TTCAAAGAGCATTGT[A/T]TATTCAAGTAGTCGT | 328572 |
| rs47457484 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ep300 | Mm_Celera | 15:81623283 | ATGTTTTAATCTCAT[C/T]TTAAGTTTTATATTT | 328572 |
| rs47568952 | snp | A/T | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81607496 | TGTATGTATGGGCTC[A/T]CATGAATGCAAAAAC | 328572 |
| rs47597133 | snp | C/G | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81599739 | TCTGTCCTCAGCTCC[C/G]GAGTGCTAGGGCTCT | 328572 |
| rs47689135 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Ep300 | Mm_Celera | 15:81601362 | GTTGGCTGCAGGCAA[C/T]GGACAAGGGATAATG | 328572 |
| rs47749585 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81610624 | CTGCCAAGGTGAGTA[A/G]CTTTGAGGATGATAT | 328572 |
| rs47750150 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81595172 | TATACTTATATGCTG[A/G]ACATTTATGCTTTCT | 328572 |
| rs47813658 | snp | G/T | | | intron-variant | Ep300 | Mm_Celera | 15:81645254 | TGGTGTTGCATTGTG[G/T]CTTAAAGGATAAGCA | 328572 |
| rs47965356 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81636536 | TTCTAACTCTGAATT[A/G]AGAGCAGCTGCCCTT | 328572 |
| rs47978755 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81634168 | AGTGGTCTTAGACTG[C/T]TGTCTGTCCAATACT | 328572 |
| rs48017744 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81616532 | ATAAAGAATTCACTC[C/T]CATCCTTCATAAGGA | 328572 |
| rs48027534 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81608011 | GCTTGATAGAATTTT[G/T]CAGTAAGCACCTTTA | 328572 |
| rs48046422 | snp | C/T | | | intron-variant | Ep300 | Mm_Celera | 15:81624037 | GTTTATAAGTTAAAG[C/T]GTGAGTTCAGGCTAA | 328572 |
| rs48075888 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81594235 | GTCCTGGTGTCCTGA[A/G]GTAGAATCACTGTGC | 328572 |
| rs48228660 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ep300 | Mm_Celera | 15:81616295 | CAGACTTGGTTTAAT[C/G]TATACCCCACAGGTA | 328572 |
| rs48250450 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ep300 | Mm_Celera | 15:81640805 | TAAAGACTAACAACA[C/T]GCTGAATATGATACG | 328572 |
| rs48265736 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ep300 | Mm_Celera | 15:81625965 | TCTCATTCACATTAC[C/T]GTAATTTCTTATTTC | 328572 |
| rs48294479 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81637181 | CCAGTTTTAAACTAT[A/G]AAGAGCAGCTGAGTA | 328572 |
| rs48318568 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Ep300 | Mm_Celera | 15:81645271 | TTAAAGGATAAGCAT[G/T]GTTTATCTAGTCCTG | 328572 |
| rs48323100 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81634097 | AACGTAAGTAACTAC[A/G]TTTTGAATCTGCTCT | 328572 |
| rs48519966 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81590633 | AGTTTTTGAATACTT[A/G]TTGAACTGATTATAT | 328572 |
| rs48572322 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81634274 | CTTCTCACATAGAGG[G/T]ACCTGTACTTTTATC | 328572 |
| rs48613765 | snp | C/T | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81590880 | AAACCAATCTCTCTA[C/T]CCCAGTTTCAAAGAC | 328572 |
| rs48655407 | snp | G/T | | | intron-variant | Ep300 | Mm_Celera | 15:81590958 | TTAGTGTATACTAGT[G/T]TATACTAGAGAACTG | 328572 |
| rs48698029 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81637461 | AGTGTTTACTGATAA[C/T]TACGGTCTTAAAAGG | 328572 |
| rs48724242 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81616586 | AGTATGTACACACAC[A/G]CAAAACGTGTAGTCT | 328572 |
| rs48752033 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81629940 | TTAGAACTTTGAACA[C/T]GCATGTCTTTAACAT | 328572 |
| rs48763859 | snp | A/C | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81629168 | GGACTCGAAGCAGCT[A/C]CCTGGAACTCCAATT | 328572 |
| rs48832976 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ep300 | Mm_Celera | 15:81613161 | ATACTGTGTTTTTGT[C/T]TTCTCTAGCAATTTT | 328572 |
| rs48835382 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ep300 | Mm_Celera | 15:81632118 | AGCCTTCAGTGTATT[A/G]ACTCATCAGACTAAG | 328572 |
| rs48837997 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81603396 | CAAATGTATTAAGCT[A/C]TCTTCCCTCTAACAC | 328572 |
| rs48848611 | snp | G/T | | | intron-variant | Ep300 | Mm_Celera | 15:81590957 | GTTAGTGTATACTAG[G/T]TTATACTAGAGAACT | 328572 |
| rs48878190 | snp | C/T | 0.231111 | 0.249285 | missense | Ep300 | Mm_Celera | 15:81624617 | GGACAATTGGCTCAG[C/T]CTGGGTCACTCAATC | 328572 |
| rs48891674 | snp | C/T | | | intron-variant | Ep300 | Mm_Celera | 15:81596705 | GTCTAGAACTCAAGA[C/T]ATCTGCCTGAGTGCT | 328572 |
| rs48988899 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Ep300 | Mm_Celera | 15:81624738 | TTAGTTCTTGCATGT[A/C]TGTTCTTCCATGTGT | 328572 |
| rs48990128 | snp | C/G | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81625168 | CAAAATCTGAAAGAA[C/G]TGGAGGGTCAGGAAT | 328572 |
| rs49033130 | snp | A/G | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81634144 | CACAGGATTGTTCTC[A/G]CATGTAGAAGTGGTC | 328572 |
| rs49039766 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81608024 | TTGCAGTAAGCACCT[A/T]TACCTGCTAAGCGAT | 328572 |
| rs49120737 | snp | G/T | | | intron-variant | Ep300 | Mm_Celera | 15:81637170 | TCAGTACAAACCCAG[G/T]TTTAAACTATAAAGA | 328572 |
| rs49227714 | snp | C/T | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81590845 | GTGTGGATAACTGAA[C/T]TGGCTTGGATTTATG | 328572 |
| rs49402200 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ep300 | Mm_Celera | 15:81620943 | CAGATCTGCCTACCT[C/T]TGCCTCTACAGCCAG | 328572 |
| rs49454721 | snp | A/G | | | utr-variant-3-prime | Ep300 | Mm_Celera | 15:81651004 | CTTGTAGTATTTTGG[A/G]AGCAAAAGATTATTT | 328572 |
| rs49506435 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Ep300 | Mm_Celera | 15:81613366 | AAAGAATCAACAAAG[C/T]CAGCCATCTGGACAG | 328572 |
| rs49514239 | snp | C/G | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81626704 | CCTTGGCCTTTAACT[C/G]AGAGAACAAACCTTT | 328572 |
| rs49545920 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ep300 | Mm_Celera | 15:81641214 | GACTACTGTAGCGTT[C/T]TCTAACACAAATGAT | 328572 |
| rs49564481 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81645494 | TTTGTAAGTGCTTAG[C/T]GTTAGACTTAAGACT | 328572 |
| rs49620780 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ep300 | Mm_Celera | 15:81634923 | AAACTTTAAATCAGT[A/G]AGACTCTGAGGTTAG | 328572 |
| rs49690411 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81643315 | GGGCTTCATTTCAGC[A/T]CTAAGGGTCCCAGAC | 328572 |
| rs49839098 | snp | A/C | 0.32 | 0.24 | intron-variant | Ep300 | Mm_Celera | 15:81590465 | CAGTCCTAGAACTCA[A/C]CATGAAGACCATTCT | 328572 |
| rs49861390 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ep300 | Mm_Celera | 15:81643383 | CTTAGAACGAAGAGG[C/T]TCTGTATTTCTAAGT | 328572 |
| rs49862017 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ep300 | Mm_Celera | 15:81595681 | TTTCTGGCTTTAGTA[A/G]AGGTGGTCTTTCTCA | 328572 |
| rs49877702 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ep300 | Mm_Celera | 15:81620950 | GCCTACCTTTGCCTC[C/T]ACAGCCAGCTTTAGC | 328572 |