| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs3658361 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4632903 | TGCTAAGTCTTGAGG[C/T]AGGGGCATTTGGGAG | 13982 |
| rs3658423 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Esr1 | Mm_Celera | 10:4632941 | AATCATCGGAGGGTA[A/G]TGTGTTTGGAGCCCA | 13982 |
| rs3659113 | snp | A/C | 0.46281 | 0.131194 | intron-variant | Esr1 | Mm_Celera | 10:4633070 | TTTACTATATTTTTA[A/C]TATCTTCTATGTAAT | 13982 |
| rs3659700 | snp | C/G | 0.46875 | 0.121031 | intron-variant | Esr1 | Mm_Celera | 10:4633163 | TCATAAACATCTCTT[C/G]TTTCATTCACCAACA | 13982 |
| rs3661006 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Esr1 | Mm_Celera | 10:4633374 | AAAACTCAGCGGCTG[A/G]CGATAACAAAGAATA | 13982 |
| rs3666332 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Esr1 | Mm_Celera | 10:4679669 | CGGATTAAAGGCGTG[C/T]GCCACCACTGCCTGG | 13982 |
| rs3692364 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Esr1 | Mm_Celera | 10:4648483 | GGAAATTCCAGATAA[A/C]ATTAACAGACAAGAC | 13982 |
| rs3692851 | snp | G/T | 0.495 | 0.0497494 | intron-variant | Esr1 | Mm_Celera | 10:4648513 | CCAGTTATTTGACAC[G/T]TGCTGTGTACTATCT | 13982 |
| rs3695463 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4961994 | ATGTGTCTTTCTGTG[C/T]CTACCTCATTTCACT | 13982 |
| rs3695482 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4962008 | GCCTACCTCATTTCA[C/T]TTAAACTGATATTCT | 13982 |
| rs3695548 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4962050 | CACATTGTTGAAAAT[A/G]ACAGTATTTCCTTCA | 13982 |
| rs3696067 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4962076 | CTTCATTTTTAGGGC[C/T]GAATGGTATTTCATT | 13982 |
| rs3696090 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4962091 | TGAATGGTATTTCAT[C/T]ATAAACATATATGTC | 13982 |
| rs3696105 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4962094 | ATGGTATTTCATTAT[A/G]AACATATATGTCTAT | 13982 |
| rs6152019 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4689264 | TGCACCCCAAATTTT[C/T]ACTTCAACTCTGCAC | 13982 |
| rs6171601 | snp | A/C | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4888213 | TGGTGTTTTAGCTTC[A/C]GTGATATTTGGGGTG | 13982 |
| rs6172752 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4888430 | ATTGTTTGGAAGCTG[C/T]ACTGATGCANCATGT | 13982 |
| rs6172769 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4888440 | AGCTGNACTGATGCA[A/G]CATGTGATAATAATC | 13982 |
| rs6173906 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4888632 | ATTTAATCTTTTATG[C/T]AACATCTTTGTCATT | 13982 |
| rs6185923 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Esr1 | Mm_Celera | 10:4967917 | TATAGCATCACTCAA[C/T]GAGGTCACAAATATT | 13982 |
| rs6187095 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Esr1 | Mm_Celera | 10:4968150 | TGAAATGCTTTTTAC[A/G]AAGGCCAAATAAATG | 13982 |
| rs6191643 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4889606 | GAAGATGATAGGTAT[A/G]CATGAAACAGANGTA | 13982 |
| rs6191672 | snp | G/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4889618 | TATNCATGAAACAGA[G/T]GTAAGGAATGAAAGA | 13982 |
| rs6192204 | snp | A/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4889710 | TAAAAACAGTCTTTG[A/T]TAACAAAATAGTGTA | 13982 |
| rs6198063 | snp | G/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4777691 | aagcaactaagggca[G/T]taaaggatttatttt | 13982 |
| rs6198557 | snp | A/C | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4777761 | actcaagcagtaatt[A/C]gaagcagaaaccagg | 13982 |
| rs6205664 | snp | A/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4889924 | CACCAAGTACCAATA[A/T]GTTTGTATGTTGGAG | 13982 |
| rs6206131 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4889966 | AATTACTCCAGTTCA[A/G]NATTTTATacacaca | 13982 |
| rs6206132 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4889967 | ATTACTCCAGTTCAN[A/G]ATTTTATacacacac | 13982 |
| rs6206193 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4890005 | cacacacacacacTC[C/T]TGTGAGGATTAGTTT | 13982 |
| rs6212017 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4777947 | ttggcaatccctcaG[C/T]CTCCAAGTCTTNCAC | 13982 |
| rs6212036 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Esr1 | Mm_Celera | 10:4777959 | caGNCTCCAAGTCTT[C/T]CACTCACTGAGTGTG | 13982 |
| rs6222763 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Esr1 | Mm_Celera | 10:4633197 | AGTTACAAAAAAGCC[A/G]CAGAAATTACCATCA | 13982 |
| rs6224315 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Esr1 | Mm_Celera | 10:4633405 | GGGCAGAGGTTTCAT[C/T]TGGGCAATCGGTTGG | 13982 |
| rs6225003 | snp | C/T | 0.375 | 0.216506 | intron-variant | Esr1 | Mm_Celera | 10:4633572 | TCTTGTTGTTGGCTC[C/T]GTGATTGTAAGGAAA | 13982 |
| rs6273868 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | GRCm38.p3 | 10:4972689 | ccttccttccttcct[C/T]cccccctctctttct | 13982 |
| rs6275594 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Esr1 | GRCm38.p3 | 10:4972995 | CACAGAGCAGGGGTA[C/T]CCTCAGGCAATGAAA | 13982 |
| rs6276612 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Esr1 | Mm_Celera | 10:4973182 | ACACTGCTTGTTTAT[A/G]TGTTAGAAGGACCTT | 13982 |
| rs6276710 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Esr1 | Mm_Celera | 10:4973247 | GCTCACTGCTCAGTG[C/T]TTGCTCCTTTATTGT | 13982 |
| rs6278514 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4821138 | CCAGCTCCCAGTGCC[A/G]TGGGGGTTAAGGAGA | 13982 |
| rs6280088 | snp | A/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4821496 | TACGTTAGTTCTTTT[A/T]AAAAAAATCAATTTC | 13982 |
| rs6280657 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4821594 | TAGTGTTTTAAAGAA[A/G]TACCTTTTAAAAAAA | 13982 |
| rs6333637 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4943342 | TTTTGAAACTAAAAC[A/G]CAGTGTGCTGCCATC | 13982 |
| rs6333706 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Esr1 | Mm_Celera | 10:4943379 | TCATGATCAGAGGGC[A/G]TGATTCCTAGCCAGT | 13982 |
| rs6346689 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Esr1 | Mm_Celera | 10:4943411 | TCCATATAAAAGAGA[A/G]TTATTGCCTGATTTA | 13982 |
| rs6358061 | snp | A/T | 0.32 | 0.24 | intron-variant | Esr1 | Mm_Celera | 10:4679450 | AAAGCACTCTTGAAA[A/T]ttttattatattatt | 13982 |
| rs6358149 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4679521 | TGGTTACATGAATTG[C/T]GAGNCATAATTTTCA | 13982 |
| rs6358168 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4679525 | TACATGAATTGNGAG[A/G]CATAATTTTCACTGt | 13982 |
| rs6358607 | snp | A/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4679572 | agggtttctctgtgt[A/T]gccntggctgtcctg | 13982 |
| rs6358625 | snp | A/C/G | 0.5 | 0 | intron-variant | Esr1 | GRCm38.p3 | 10:4679576 | tttctctgtgtngcc[A/C/G]tggctgtcctggaac | 13982 |
| rs6359159 | snp | C/T | 0.32 | 0.24 | intron-variant | Esr1 | Mm_Celera | 10:4679709 | ACTGTTTTTTAATAA[C/T]ACTCCAGTTATTGCA | 13982 |
| rs6359200 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Esr1 | Mm_Celera | 10:4679737 | GCACATAATTGATAT[A/G]TAACTGTAACTAATA | 13982 |
| rs6359643 | snp | G/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4679796 | TAAAACTGGAGAAAA[G/T]AATATTAAATGACAA | 13982 |
| rs6362175 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Esr1 | Mm_Celera | 10:4877946 | AGTCAGTGTGGGCAG[A/T]GTACCTACAGCTGGG | 13982 |
| rs6363203 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Esr1 | Mm_Celera | 10:4878116 | gtgaatggattaaag[C/T]attgtatgatgagtc | 13982 |
| rs6376063 | snp | A/G | 0.5 | 0 | intron-variant | Esr1 | GRCm38.p3 | 10:4687129 | tgtgtgtgtgtgtgt[A/G]tAGAATTCACAGTGG | 13982 |
| rs6376563 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4687198 | ACGGTTGTTATTATG[C/T]GTACAATAGGTtgat | 13982 |
| rs6409936 | snp | C/G | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4623304 | TCCTTCTAAGGCATG[C/G]ATCCAAATTCCTCCA | 13982 |
| rs6410065 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4623391 | AGCAAGAGATTAGTG[C/T]ATTAGTGAGGACAGA | 13982 |
| rs6411121 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4623530 | TTTGGCCTTTTTTTT[C/T]CAGAGCTCTCAGATA | 13982 |
| rs6411650 | snp | C/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4623612 | AGAGATTGTGTAATT[C/T]CCTGCAGATACCTTG | 13982 |
| rs6411677 | snp | A/T | 0.5 | 0 | intron-variant | Esr1 | Mm_Celera | 10:4688984 | AACAAATCATTTTTT[A/T]AAAAAATGATATCAT | 13982 |
| rs8244291 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Esr1 | Mm_Celera | 10:4710029 | AGACAGCAAGGCTCC[C/T]GGACTCCCGCTGCCA | 13982 |
| rs8244292 | snp | A/G | 0.341797 | 0.232537 | intron-variant, utr-variant-5-prime | Esr1 | GRCm38.p3 | 10:4711952 | AGCAAAGGGACCTCC[A/G]GNAGCCGCGCCCCTA | 13982 |
| rs8244293 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Esr1 | Mm_Celera | 10:4712254 | AAGTCCCCCTTGGCA[C/G]GAGTACTGGCCCTGG | 13982 |
| rs13480470 | snp | C/T | 0.413728 | 0.188926 | intron-variant | Esr1 | Mm_Celera | 10:4637805 | TCACCATGTGATTAT[C/T]ATGCATTGCCATGGG | 13982 |
| rs16783368 | snp | C/T | 0.090703 | 0.192677 | utr-variant-3-prime | Esr1 | GRCm38.p3 | 10:5001922 | GGGGCTCAAGATTTC[C/T]CTTTAATAAAGTCAC | 13982 |
| rs16783369 | snp | C/T | 0.0867769 | 0.189363 | utr-variant-3-prime | Esr1 | Mm_Celera | 10:5001848 | AGATCGCTTTGTCAA[C/T]GACTTCAATTAAAGG | 13982 |
| rs16783370 | snp | G/T | 0.0928019 | 0.194393 | utr-variant-3-prime | Esr1 | GRCm38.p3 | 10:5001442 | GATTCTCAGAACCTT[G/T]CGGGGAGCCTGGGAG | 13982 |
| rs16783371 | snp | C/T | 0.113866 | 0.209684 | synonymous-codon | Esr1 | Mm_Celera | 10:4939288 | TCTGATGATTGGTCT[C/T]GTCTGGCGCTCCATG | 13982 |
| rs16783372 | snp | A/G | 0.0849383 | 0.187762 | intron-variant | Esr1 | Mm_Celera | 10:4857575 | CTTTATTGAGAACCA[A/G]TTTTTCCATAAATAA | 13982 |
| rs16783373 | snp | A/G | 0.090703 | 0.192677 | intron-variant | Esr1 | Mm_Celera | 10:4857443 | TCAAAACACTTGGAT[A/G]AACACTTCATTACAA | 13982 |
| rs16783374 | snp | A/G | 0.0886966 | 0.191001 | intron-variant | Esr1 | Mm_Celera | 10:4857416 | NACATGCTAATTTTG[A/G]CCCGTCTTTGCTCAA | 13982 |
| rs16783375 | snp | C/G | 0.0867769 | 0.189363 | intron-variant | Esr1 | Mm_Celera | 10:4857401 | CAGACTAAAACCTNG[C/G]ACATGCTAATTTTGN | 13982 |
| rs16783376 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Esr1 | Mm_Celera | 10:4857399 | AGCAGACTAAAACCT[C/T]GNACATGCTAATTTT | 13982 |
| rs16783377 | in-del | -/G | 0.0867769 | 0.189363 | intron-variant | Esr1 | Mm_Celera | 10:4857303 | ATTAGGGAGATGGNN[-/G]TATTGGGATTTGTCA | 13982 |
| rs16783378 | snp | A/T | 0.0867769 | 0.189363 | intron-variant | Esr1 | GRCm38.p3 | 10:4857301 | GATTAGGGAGATGGN[A/T]NTATTGGGATTTGTC | 13982 |
| rs16783379 | snp | C/G | 0.0867769 | 0.189363 | intron-variant | Esr1 | Mm_Celera | 10:4857301 | GGATTAGGGAGATGG[C/G]NNTATTGGGATTTGT | 13982 |
| rs16783380 | snp | A/T | 0.0849383 | 0.187762 | intron-variant | Esr1 | Mm_Celera | 10:4857217 | GCTAAACTCAACTTC[A/T]ATGTTAAGAGTGAAT | 13982 |
| rs16783381 | snp | C/G | 0.0928019 | 0.194393 | intron-variant | Esr1 | Mm_Celera | 10:4713249 | AAAAGACTAATAAAT[C/G]TCCCCTGGGCTCCAC | 13982 |
| rs16783382 | snp | A/G | 0.209751 | 0.246739 | intron-variant | Esr1 | GRCm38.p3 | 10:4713218 | TGGCCTCAAACACCT[A/G]CAGCTTTAAATAATA | 13982 |
| rs16783383 | snp | A/G | 0.24013 | 0.249805 | intron-variant | Esr1 | GRCm38.p3 | 10:4713180 | TCCTTGCTAGCACAG[A/G]CCACCTGGACCTTTA | 13982 |
| rs16783384 | snp | A/G | 0.090703 | 0.192677 | intron-variant | Esr1 | GRCm38.p3 | 10:4713131 | TAACTTCTTTGGACT[A/G]NTTTCCAATTCTTGT | 13982 |
| rs16783385 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Esr1 | GRCm38.p3 | 10:4713130 | AACTTCTTTGGACTN[G/T]TTTCCAATTCTTGTG | 13982 |
| rs16783386 | snp | A/G | 0.0867769 | 0.189363 | intron-variant | Esr1 | GRCm38.p3 | 10:4713108 | ATTCTTGTGTAATTA[A/G]GGGACAGGGNCGTTT | 13982 |
| rs16783387 | snp | C/T | 0.0867769 | 0.189363 | intron-variant | Esr1 | Mm_Celera | 10:4713098 | AATTANGGGACAGGG[C/T]CGTTTGGATCTGTCT | 13982 |
| rs16783388 | snp | A/C/T | 0.367769 | 0.260363 | intron-variant | Esr1 | GRCm38.p3 | 10:4712962 | TGCCAAAGAATCCTT[A/C/T]CTGACTTCCCCGAGG | 13982 |
| rs16783389 | snp | C/G | 0.0867769 | 0.189363 | intron-variant | Esr1 | Mm_Celera | 10:4712945 | TGACTTCCCCGAGGG[C/G]TGGGANGGGGAGACC | 13982 |
| rs16783390 | snp | G/T | 0.35124 | 0.228584 | intron-variant | Esr1 | GRCm38.p3 | 10:4712939 | CCCCGAGGGNTGGGA[G/T]GGGGAGACCTGCAGC | 13982 |
| rs16821018 | snp | C/T | 0.099723 | 0.199792 | upstream-variant-2KB, intron-variant | Esr1 | GRCm38.p3 | 10:4708534 | NGAAAGGGGTTGTGG[C/T]GGNAAGCATGGCCNC | 13982 |
| rs16821019 | snp | A/G | 0.104938 | 0.20361 | upstream-variant-2KB, intron-variant | Esr1 | GRCm38.p3 | 10:4708531 | AAGGGGTTGTGGNGG[A/G]AAGCATGGCCNCCAT | 13982 |
| rs16821020 | snp | A/G | 0.099723 | 0.199792 | upstream-variant-2KB, intron-variant | Esr1 | GRCm38.p3 | 10:4708520 | GNGGNAAGCATGGCC[A/G]CCATCTTGGTTCCCC | 13982 |
| rs16821021 | snp | C/G | 0.095 | 0.19615 | upstream-variant-2KB, intron-variant | Esr1 | Mm_Celera | 10:4708491 | CCCACTCACCACCCG[C/G]CACCGCTACTCTGGC | 13982 |
| rs16821022 | snp | A/C | 0.18 | 0.24 | upstream-variant-2KB, intron-variant | Esr1 | GRCm38.p3 | 10:4708398 | CTGTACTGCTTGCCC[A/C]GGTGTAGGGGAGAAC | 13982 |
| rs16821023 | snp | A/C | 0.188366 | 0.242283 | upstream-variant-2KB, intron-variant | Esr1 | GRCm38.p3 | 10:4708342 | GTGCAGACTCTGGAC[A/C]AAACACCCAACATCA | 13982 |
| rs16821024 | snp | A/T | 0.090703 | 0.192677 | upstream-variant-2KB, intron-variant | Esr1 | Mm_Celera | 10:4708303 | CCGACCCAACACTTC[A/T]CTCCGNACACAGGAC | 13982 |
| rs16821025 | snp | A/G | 0.090703 | 0.192677 | upstream-variant-2KB, intron-variant | Esr1 | GRCm38.p3 | 10:4708297 | CAACACTTCNCTCCG[A/G]ACACAGGACACAGCA | 13982 |
| rs16821026 | snp | C/G | 0.265928 | 0.249492 | upstream-variant-2KB, intron-variant | Esr1 | Mm_Celera | 10:4708259 | CTCTGTCTGACACTC[C/G]TATGCCTTCTATAGT | 13982 |
| rs16821027 | snp | C/T | 0.172336 | 0.23763 | upstream-variant-2KB, intron-variant | Esr1 | Mm_Celera | 10:4708203 | ATAGTTTGCACGCTC[C/T]CTTCCCATGCATTGC | 13982 |
| rs16821028 | snp | C/T | 0.090703 | 0.192677 | upstream-variant-2KB, intron-variant | Esr1 | Mm_Celera | 10:4708160 | AGCGGCCTCTTACCT[C/T]ACTTGTCTAAGTGCA | 13982 |