SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3698658 | snp | A/G | 0.5 | 0 | intron-variant | Epn2 | GRCm38.p3 | 11:61527477 | CACCATAGTCTAAAA[A/G]GGTCATATACTGCCC | 13855 |
rs6338513 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Epn2 | GRCm38.p3 | 11:61528093 | ATCTGAGCTCCTAAC[A/G]CACAAGAGCCCTGCC | 13855 |
rs6340658 | snp | A/C | 0.5 | 0 | intron-variant | Epn2 | GRCm38.p3 | 11:61528509 | ggaatgcaatgcctt[A/C]gtctggcttccacag | 13855 |
rs26941068 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Epn2 | GRCm38.p3 | 11:61543737 | TTTTCTACTCCTACA[C/T]TGGGAACAGTGGCTT | 13855 |
rs26941069 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Epn2 | GRCm38.p3 | 11:61543174 | TGTAAAGCTGGTCTT[C/T]CTTACCTTTCCAAAC | 13855 |
rs26941070 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Epn2 | GRCm38.p3 | 11:61543074 | AGAACAGATCCTAAG[C/T]AAGTGGTAGCAAAAT | 13855 |
rs26941071 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61542549 | GGAATTCTCCCAACC[A/C]TTCTCAAGTGCTTCT | 13855 |
rs26941072 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61541685 | CTGGCTTTTATCAGG[A/G]TATAGCAGCAGCTCT | 13855 |
rs26941073 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Epn2 | GRCm38.p3 | 11:61541523 | ACTACCAGCGCTGCC[A/G]TGGTTCCTACACTAC | 13855 |
rs26941074 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Epn2 | GRCm38.p3 | 11:61541393 | AGCTCAAGGATCCCC[A/G]ACATTTTCCTAGGGA | 13855 |
rs26941075 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Epn2 | GRCm38.p3 | 11:61541277 | AAATCCTCTGTGAAG[C/T]GAGCCCAGCAAAGAC | 13855 |
rs26941076 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61540820 | CTTAACCACACTGAC[C/T]TCATTCACCTGCTTT | 13855 |
rs26941077 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61540264 | ATAGATCAGGTTCTA[G/T]GGACCACAAGCCCAG | 13855 |
rs26941078 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61539275 | AGTGAGAGCTGAGCA[A/G]GCTGACTTACCTGGG | 13855 |
rs26941079 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Epn2 | GRCm38.p3 | 11:61537575 | CTTATTTAGAGACAC[G/T]CTAGCCTCAGTGATG | 13855 |
rs26941080 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61537080 | TTGAAAACTGGGGAA[A/T]GAATGGTTAACAAAC | 13855 |
rs26941081 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Epn2 | GRCm38.p3 | 11:61537006 | TAGACATCTCTAGGA[C/G]GCATACATGGGAAAT | 13855 |
rs26941082 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Epn2 | GRCm38.p3 | 11:61536701 | TCCTACCCAATTATA[C/G]TTTTCATTGGACCTC | 13855 |
rs26941083 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61535777 | AGGCATGCTTAGGAA[A/G]AGGAAGCCCACACAG | 13855 |
rs26941084 | snp | C/T | 0.408163 | 0.193609 | synonymous-codon | Epn2 | GRCm38.p3 | 11:61535367 | CTCTAACTCAGAGGA[C/T]ACTCGTGGGGAAGTA | 13855 |
rs26941085 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Epn2 | GRCm38.p3 | 11:61535056 | TCACTCGGAGTTAGC[C/T]GTTTCTCTGGACACT | 13855 |
rs26941086 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Epn2 | GRCm38.p3 | 11:61535020 | TCAGAAGTCCCTGGA[C/G]AGTAAGTCTACATAG | 13855 |
rs26941087 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61534883 | CCACACATCTGCCAC[A/G]GGATATATTGCCCTG | 13855 |
rs26941088 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61534863 | CCTTCTAGCCTTCTA[A/G]TCTCCCACACATCTG | 13855 |
rs26941089 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61533847 | TTCCCAGAGGACTCA[C/T]GGAGGTTCCTCCTTC | 13855 |
rs26941090 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61533168 | CACATCAGGTGATAC[A/C]ACTAGTATGCCTGGC | 13855 |
rs26941091 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61533138 | GCAACATCTATCATC[A/G]GGGCCCTGTGGCACC | 13855 |
rs26941092 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61533002 | ATCATCATCCCTCTT[C/T]ACCTGCCTTTGGTTT | 13855 |
rs26941093 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61532825 | AACTTGGAAATTGAG[C/T]TGCTCCAATCCCAAA | 13855 |
rs26941094 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61532813 | TAACTCCTGAATAAC[A/T]TGGAAATTGAGCTGC | 13855 |
rs26941095 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61532776 | TAATATTAGTTCTCA[C/G]CACAGCACAGGCCTT | 13855 |
rs26941096 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61532353 | ATTATGACTTCTTGA[A/G]CTTGAGCTGGGTGCA | 13855 |
rs26941097 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61531921 | ACAGAGCCTAGCATT[A/T]GGTATACTTTAACAA | 13855 |
rs26941098 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61531892 | TGGGTGTCCCAGATA[A/C]TTCATATGGGAGGAC | 13855 |
rs26941099 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61531843 | GGTTCACACAGCACT[A/G]CTCGCTGCTACCAGG | 13855 |
rs26941100 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61531797 | GATGCTCAACTCACT[A/G]TTCTGATCTGACAAG | 13855 |
rs26941101 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61531685 | TCTACCTGCTGCCCA[C/T]GTCACAATGCATGGG | 13855 |
rs26941102 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61530882 | TGGCAAATTTCATCT[C/T]CATTTGAAGAGCAAG | 13855 |
rs26941103 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61530858 | TCCAGTTTTGTTAAA[C/T]AGTCGGAATGGCAAA | 13855 |
rs26941104 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61530789 | TCTACCTAGTAACAA[C/T]AGTTATACAGCTCTG | 13855 |
rs26941105 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61530749 | GAGTATGGATTCTTT[C/T]TGGAGTAATGGAAAC | 13855 |
rs26941106 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61530732 | GCTGGTGGCTAGGAG[C/T]TGAGTATGGATTCTT | 13855 |
rs26941107 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61530531 | AATGCAAATGTCCAA[C/T]GGGAGGAGAGTGTAC | 13855 |
rs26941108 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61529464 | AGGCCTTCTGAATTA[A/C]CAGGCTGTGAGGCCT | 13855 |
rs26941109 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61529321 | TTCATGTGCACAGCC[A/G]GCAGTCACAGTCCAT | 13855 |
rs26941110 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61529087 | ACGAGGCTGGCCCGC[C/T]GCCCTTAGGAGAGAG | 13855 |
rs26941111 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61528702 | CACCACCAGTCTGGA[C/T]ACCTGCAACACTCCT | 13855 |
rs26941112 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61528617 | AAGACAATGCAAAGA[C/T]TAGGAGTCTGAGAGG | 13855 |
rs26941113 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61528127 | GGCCCTCTCAGGCAA[A/G]AGCCACCTAGCTCAA | 13855 |
rs26941114 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61527884 | CTGAGAATCCACACA[G/T]GAAGAACCCCAAGGG | 13855 |
rs26941115 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61527719 | CTAAGTGAAGGTACA[A/G]GCCTCTGGGTAAGTG | 13855 |
rs26941116 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61527598 | CCATGGGGACAGAAC[A/G]CGCAGTTGGCTTTCC | 13855 |
rs26941117 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61527564 | CAGGATCTGCAAAGT[A/G]AGCTTCCCTCTCCCT | 13855 |
rs26941118 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61527446 | AATACTCCACCAAAG[A/T]GTTTTCCCCTCACCT | 13855 |
rs26941119 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61527263 | TCTCTCAGCTAGATA[A/G]ATACACTTGAGGGAC | 13855 |
rs26941120 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61527027 | CTACAGGGGTGGTAC[C/T]TCATCAGGCATGGCT | 13855 |
rs26941121 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61526845 | TATTTGGCCTTTCTG[G/T]TTCTAATGCTCCAGA | 13855 |
rs26941122 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61526737 | GGCTTGCTGCAGTGA[C/T]ACACCCAAAAGTTGT | 13855 |
rs26941123 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61526606 | AAGGCTTACTTGGGT[C/G]CTGCTCAGATATTGC | 13855 |
rs26941124 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61526169 | ACACAGCTTCCATGC[C/T]TAGCCTGGCCAGACT | 13855 |
rs26941125 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn2 | Mm_Celera | 11:61524708 | GGTTATCTCTGCCTA[A/G]CTAACCTCAGCAGCA | 13855 |
rs26941126 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Epn2 | Mm_Celera | 11:61524589 | GTGGTGCATATGAAG[C/T]CTATTTTGCAACCGT | 13855 |
rs26941127 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | Mm_Celera | 11:61524570 | TTTTTCCATTTGTGT[C/T]GAAGTGGTGCATATG | 13855 |
rs26941128 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | Mm_Celera | 11:61524499 | TCTAACAGTTTATAA[C/T]CCTCTCAGCAGGTCC | 13855 |
rs26941129 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Epn2 | Mm_Celera | 11:61524477 | CCAGCACCGTTTCCA[C/T]GCTGGTTCTAACAGT | 13855 |
rs26941130 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | Mm_Celera | 11:61524202 | GAAACAATATGCTGG[A/G]TAGCTATGCCAGATT | 13855 |
rs26941131 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn2 | Mm_Celera | 11:61524140 | ATTTCCAGATCCACC[A/G]CAAAGTGTCCTGAGC | 13855 |
rs26941132 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Epn2 | Mm_Celera | 11:61524139 | CATTTCCAGATCCAC[C/T]GCAAAGTGTCCTGAG | 13855 |
rs26941133 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Epn2 | Mm_Celera | 11:61523798 | AATTTTGAGCAACAA[A/C]GGTTAGTCAACTTAG | 13855 |
rs26941134 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | Mm_Celera | 11:61523545 | TTCCCATCACACAAG[A/G]GGCTCACAGGGGTTC | 13855 |
rs26941135 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | Mm_Celera | 11:61523500 | TCTGGCAAGTGCACC[A/G]AGAGGCAAAGCTAAA | 13855 |
rs26941136 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Epn2 | Mm_Celera | 11:61523418 | CACATATACACAGAG[C/G]ACACCAGTAAGAATA | 13855 |
rs26941137 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn2 | Mm_Celera | 11:61523214 | GAAGTCAGAGTCAAA[A/G]TTCAGAACAGGGGCT | 13855 |
rs26941138 | snp | C/T | 0.32 | 0.24 | missense | Epn2 | GRCm38.p3 | 11:61523068 | CTCCCCAGGCATCTG[C/T]TGTCTTTCCAGCATT | 13855 |
rs26941139 | snp | A/C | 0.32 | 0.24 | intron-variant | Epn2 | Mm_Celera | 11:61523000 | AGAAGTAGTGAAGCT[A/C]TAGGAACCAGGCTGA | 13855 |
rs26941140 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | Mm_Celera | 11:61522831 | GGTCAGTCTGCCACC[C/T]AGAAAGGAGACCAGA | 13855 |
rs26941141 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Epn2 | Mm_Celera | 11:61522761 | CAGTGTAGGAAATAC[A/G]TGTTGTTCTGGACAT | 13855 |
rs26941142 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Epn2 | Mm_Celera | 11:61522685 | GGCAACAGGTGGGAT[A/C]AGAGAACACAAGTGC | 13855 |
rs26941143 | snp | A/C | 0.32 | 0.24 | intron-variant | Epn2 | Mm_Celera | 11:61522660 | CTTCAGTCACTTGCT[A/C]GACTGGGAAGGCAAC | 13855 |
rs26941144 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Epn2 | Mm_Celera | 11:61522608 | AGGGGCTTCTCTCCC[A/T]GGTACTCCACATCAT | 13855 |
rs26941145 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn2 | Mm_Celera | 11:61522512 | GGGGACATACAAGCT[A/G]GTGACTGAAAGCATC | 13855 |
rs26941146 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Epn2 | Mm_Celera | 11:61522083 | ATTTGGGGTTGGTGG[C/T]AAAGCACAGATGTGT | 13855 |
rs26941147 | snp | G/T | 0.391111 | 0.206368 | synonymous-codon | Epn2 | Mm_Celera | 11:61521770 | ACTCAGGTGTTTTCC[G/T]GGCACTGCTAGGCTT | 13855 |
rs26941148 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Epn2 | Mm_Celera | 11:61520836 | GTTGGAGTTGACACT[C/G]CTGGAGATACAGTTC | 13855 |
rs26941149 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Epn2 | Mm_Celera | 11:61520530 | TTGTAAGCAAGGCCT[A/T]CCACAGTGCTAGACC | 13855 |
rs26941150 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | Mm_Celera | 11:61520458 | TCTACCCATGTAGCT[C/T]GGATATCTGCCAAAA | 13855 |
rs26941151 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Epn2 | Mm_Celera | 11:61520405 | ACCCTAGGTTCAAAG[A/G]GGCTGTGTAGCCCCT | 13855 |
rs26941152 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Epn2 | Mm_Celera | 11:61519807 | CACTTTTGGCATTCC[A/T]GAAGTGATCTGAAGG | 13855 |
rs26941153 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Epn2 | Mm_Celera | 11:61519800 | CTGCCTCCACTTTTG[C/G]CATTCCAGAAGTGAT | 13855 |
rs26941154 | snp | G/T | 0.124444 | 0.216185 | missense | Epn2 | Mm_Celera | 11:61519621 | ATGCACTGCTTCCCA[G/T]GACAGGGCTTCCCCG | 13855 |
rs26941155 | snp | A/T | 0.260355 | 0.249785 | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61519010 | CAAAGGAAAATAAAA[A/T]ATGCACAACCACTTC | 13855 |
rs26941156 | snp | A/G | 0.497778 | 0.0332592 | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518501 | CAGAGTCAACTGACT[A/G]ATAATTCATCAAAAG | 13855 |
rs26941157 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518322 | CCAGCCACATTTCTG[A/G]CCTGCAGTAAATGGA | 13855 |
rs26941158 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Epn2 | GRCm38.p3 | 11:61518201 | CTGGGCCAGTCTCTG[C/T]CATGACTCAGCTAGG | 13855 |
rs26941159 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61517953 | GACACAAACTGCCAG[A/G]ACCAAGAAGGGGCAG | 13855 |
rs26941160 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61517769 | GCCTAGGAGCAGCAT[A/G]TAGACTCAGACCCAG | 13855 |
rs26941161 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Epn2 | GRCm38.p3 | 11:61517686 | CCTGAATAGCAGAGC[C/T]CAAACCTTTCCCTCG | 13855 |
rs26941162 | snp | A/C | 0.391111 | 0.206368 | downstream-variant-500B | Epn2 | Mm_Celera | 11:61517177 | AAGCTGCTTCCCTAG[A/C]CAGCCCTGCCACATC | 13855 |
rs26941163 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Epn2 | Mm_Celera | 11:61517132 | CATCAAAAGCAGACC[C/T]GAGCCTGTCCTTGAG | 13855 |
rs26941164 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Epn2 | Mm_Celera | 11:61516885 | CTGACAGAGAAATCC[A/G]GTCTGTGGAGAGGTG | 13855 |
rs26941165 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Epn2 | Mm_Celera | 11:61516873 | ATAAGTGCTCAACTG[A/G]CAGAGAAATCCGGTC | 13855 |
rs26985787 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61573135 | CCCTGAGGTGTTCTG[C/T]CTGGATAGACCAAAG | 13855 |
rs26985788 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61573028 | GTGGAAAGGGGAAAT[G/T]TTTTTCTCAAACTCT | 13855 |
rs26985789 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Epn2 | GRCm38.p3 | 11:61572983 | AACCCTGAGCATTAG[C/T]TCTTTCAAAATGCAA | 13855 |
rs26985790 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61572824 | CACCAGAACTCCCAG[C/G]ATGTACCACCTCACA | 13855 |
rs26985791 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61572486 | AACAGCAAGGTCACA[A/G]AAACACACAGAACAC | 13855 |
rs26985792 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61571952 | GTATACAGAAGAGCA[C/T]CCACACCCAAGCCCA | 13855 |
rs26985793 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61571696 | GGCCTGGTGTTCCTA[A/G]AGGCTACCCTAAGCA | 13855 |
rs26985794 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61571397 | AGGAACCCTTGATGG[A/G]GATGATAAGAACCGG | 13855 |
rs26985795 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61570311 | ACACCATGTCTCCAG[C/T]CCTCTGCGCACACAG | 13855 |
rs26985796 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61570184 | CTACAGAATTGCCCA[C/T]TCACCATACCAAAAG | 13855 |
rs26985797 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Epn2 | GRCm38.p3 | 11:61569935 | CCTGGGAAACTGGCC[C/G]GGAAAGCAGTGGAAC | 13855 |
rs26985798 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61569545 | TCTCCTCCTTGGCTG[C/T]CCCAGCTCACATCAG | 13855 |
rs26985799 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61569163 | TTCCCATTTGTCCAT[A/G]AAACTGCAAATGTGG | 13855 |
rs26985800 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61568711 | AAAAGGAGGGAATGG[G/T]AAACAAACAGTCACA | 13855 |
rs26985801 | snp | A/C/T | 0.336735 | 0.234472 | intron-variant | Epn2 | GRCm38.p3 | 11:61568635 | CCTTTTCATGAACTC[A/C/T]AAGCATGACACCCAG | 13855 |
rs26985802 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61568616 | GAAGTACATGATAAG[A/G]ACTCCTTTTCATGAA | 13855 |
rs26985803 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61568517 | AGGGTACTCAGTCAC[A/T]TTTCCAGTATCTAGG | 13855 |
rs26985804 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61568465 | CTTTCTTCCACTTTC[A/G]AATGAGTTTTACACA | 13855 |
rs26985805 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61568265 | AGCCTGTTAAAAATT[C/T]CAGCTATCAACTAGG | 13855 |
rs26985806 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Epn2 | GRCm38.p3 | 11:61567983 | CTTTTCATTCATTGA[A/C]TACTCCATAATGAAA | 13855 |
rs26985807 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61567305 | AACCAGAGTTAGAAA[G/T]CGGCTTAGTGATCAG | 13855 |
rs26985808 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61566928 | CAGCAGTTCAGCTAA[C/T]AAACAGCTCAAAGAA | 13855 |
rs26985809 | snp | A/G/T | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61566821 | CTCAGACCACTGAGC[A/G/T]TGTCCTCCACACCAG | 13855 |
rs26985810 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61566750 | GGAATGGAAACCTTT[C/T]TGCCATTGGATCCCA | 13855 |
rs26985811 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61566696 | AACAGACTTAAAACT[A/T]TGTGGGCTATATAAA | 13855 |
rs26985812 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61566643 | ACTGACAAGGACAGA[A/C]TTGACCTATCTCTAG | 13855 |
rs26985813 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61566563 | CAACACATTGCTGCC[A/C]AGTAACCCCTCTAAG | 13855 |
rs26985814 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61566501 | CCATCAACAGAACAT[A/G]GGGCCACTGTCTTCC | 13855 |
rs26985815 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61566323 | AAGACTCTGAACTGA[A/G]CTGCCTAGAAGCCTC | 13855 |
rs26985816 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn2 | GRCm38.p3 | 11:61565459 | TGACAAAAATAAACC[C/T]GAAATCAGTTAACAG | 13855 |
rs26985817 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61564936 | TAGCACATACCCAGA[A/G]AAAATTTCCAGTCCA | 13855 |
rs26985818 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61564762 | GCCTGTTCCAGCTCC[C/T]TGCTTGCACCACAGT | 13855 |
rs26985819 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61563609 | CCCTGCCATGAGCAG[A/G]GTGGAGCTAGGCACC | 13855 |
rs26985820 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61561972 | GTGTCTACCTAGCAA[A/G]ATGAAGCATACAAAC | 13855 |
rs26985821 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Epn2 | GRCm38.p3 | 11:61561668 | CACATACTTAGGTCA[C/G]TGTCTACTACCTACC | 13855 |
rs26985822 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61560413 | GCAAATCTGACAGCC[C/T]CAATAATGGCAGGGA | 13855 |
rs26985823 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Epn2 | GRCm38.p3 | 11:61558016 | TGAAAACTAACTACC[A/G]CTTTGATATTTGAGG | 13855 |
rs26985824 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61557221 | ACAACCATTTGTTTG[C/T]ACCCAAGCTTCATCC | 13855 |
rs26985825 | snp | C/T | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556444 | TTTTCCTTAGAGGTA[C/T]CCCAGGTTTTTTATC | 13855 |
rs26985826 | snp | A/T | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556395 | GAGGCTGAAAGGTAA[A/T]CTCCCTTTTTTGATG | 13855 |
rs26985827 | snp | C/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556055 | TAGGAAATGATGTCT[C/T]TCTGGCTGTTGTGAT | 13855 |
rs26985828 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Epn2 | GRCm38.p3 | 11:61554843 | CAGGAGCACTCTCCT[C/T]ATATGGACTGCTCTG | 13855 |
rs26985829 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Epn2 | GRCm38.p3 | 11:61554669 | ATGACAGGTATCTAA[A/C]GAGCTCTTCCCTTAC | 13855 |
rs26985830 | snp | A/G | 0.5 | 0 | intron-variant | Epn2 | GRCm38.p3 | 11:61554646 | CTGCAGCTGAACGGA[A/G]CTGGTAAATGACAGG | 13855 |
rs26985831 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Epn2 | GRCm38.p3 | 11:61554599 | AGACAGTGGGTATTC[C/T]TGCTTTTCTGGCTAG | 13855 |
rs26985832 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61554204 | ACACTGTCTCTCCGT[A/G]CCTAGTGTAGCACCT | 13855 |
rs26985833 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61553934 | CAGGGCCCTCTTCCA[C/T]GTTTTGTTTTGTTGT | 13855 |
rs26985834 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Epn2 | GRCm38.p3 | 11:61553300 | AAGAAGTGGAACTCT[C/T]AGCCACATGCCACAA | 13855 |
rs26985835 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn2 | GRCm38.p3 | 11:61553207 | TATGCTTAATTTAGA[C/T]CTGGCTGGTGACTGG | 13855 |
rs26985836 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Epn2 | GRCm38.p3 | 11:61552796 | CTAGATGCTCTCTGC[C/T]TAGATGTTCTGTCAG | 13855 |
rs26985837 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Epn2 | GRCm38.p3 | 11:61552673 | ATACCATGTGGCATT[C/G]ATGGAAAAGAAGCAG | 13855 |
rs26985838 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Epn2 | GRCm38.p3 | 11:61552528 | GATCAAACACCCTGC[A/T]CTCTGCACAAAAGGG | 13855 |
rs26985839 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61552372 | TATTAGCAGGCTCCT[G/T]TTTAGCCCTTAGGAA | 13855 |
rs26985840 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61551951 | CAGTAATTTCTGGCT[A/G]GTTAAAAAATACCAA | 13855 |
rs26985841 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Epn2 | GRCm38.p3 | 11:61551748 | AGTGATCATTTTAGT[G/T]TGAAGAGAAAGGGCT | 13855 |
rs26985842 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Epn2 | GRCm38.p3 | 11:61551740 | TTTTTAACAGTGATC[A/G]TTTTAGTTTGAAGAG | 13855 |
rs26985843 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61550784 | GTGCAGCTAGGCAGG[A/G]AAATGCCATCCAACC | 13855 |
rs26985844 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Epn2 | GRCm38.p3 | 11:61549638 | AATTTCCAGAACCTA[C/T]GCGACAATTCAGGGA | 13855 |
rs26985845 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn2 | GRCm38.p3 | 11:61549522 | TGTCAAAGTTGTTAA[A/G]TCATTTCAGATCCAC | 13855 |
rs26985846 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Epn2 | GRCm38.p3 | 11:61548709 | AGGTTGGGCCTCATA[A/G]AAGAAAAAGACACCT | 13855 |
rs26985847 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Epn2 | GRCm38.p3 | 11:61548179 | TTCCTTCCCATCAGA[A/G]ATATAAAATACAAGG | 13855 |
rs26985848 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Epn2 | GRCm38.p3 | 11:61547911 | CCATCTCCAGCATGT[A/G]TGGTGATCGCCATCT | 13855 |
rs26985849 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61547139 | AGGTTTTTGCCGGAG[C/T]GGCTAGCTTGCAGTG | 13855 |
rs26985850 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61546919 | GCCATGCCCTAGAGA[A/G]AAAAAGAACACATTG | 13855 |
rs26985851 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Epn2 | GRCm38.p3 | 11:61546493 | AGAACCTGTCTTGAT[A/G]AGGTAGTCCAGCAGT | 13855 |
rs26985852 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Epn2 | GRCm38.p3 | 11:61546229 | AAGGTTGGGCTGGCT[A/G]GAGCCACGGCCAAAG | 13855 |
rs26985853 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Epn2 | GRCm38.p3 | 11:61546007 | CAGGGGGACCAAAAG[C/G]CCCTTTGTAAGTAAC | 13855 |
rs26985854 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Epn2 | GRCm38.p3 | 11:61544900 | AGAAAGCAACTCAAA[C/T]TTGAAAATTACGATA | 13855 |
rs45637332 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563242 | GAGAAAAAAAAAAAA[A/C]CAAAATAAGAAAGGA | 13855 |
rs46028967 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538841 | CGAACTCAGAAATCC[A/G]CCTGCCTCTGCCTCC | 13855 |
rs46348090 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575501 | ACCTTATGCTCTGAT[A/G]AAAATGGTTCTGTTT | 13855 |
rs46423086 | snp | A/C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562544 | CTGGCAAGGCTGTGG[A/C/G]GGAAATGAGCAGCCA | 13855 |
rs46577646 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531671 | TTTCCCCTCACCCTT[C/T]TACCTGCTGCCCATG | 13855 |
rs46801787 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61555604 | ACATAAAATAAATCT[C/T]TAAAAAAGGAAAAAA | 13855 |
rs46888776 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61543006 | ACTCACCTGAGTCAC[A/T]GCCTAGGACAGAGGA | 13855 |
rs47065728 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576147 | TACCATGTGGTTGCT[G/T]GGATTTGAACTCGGA | 13855 |
rs47826262 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547994 | AACACCTGAATAAAC[A/G]ATATTACACTTACAA | 13855 |
rs47990192 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562433 | TGTGATAGTATGATA[A/T]GCTCAACTTGAGAAG | 13855 |
rs48542178 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558102 | ATATACATACCTGCT[G/T]CTGTCAGGGCCAGAG | 13855 |
rs48721134 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61544696 | TGAGGGTTCCAACCC[C/G]CTTTGTATCCTCCAC | 13855 |
rs48859692 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61543400 | GTTGGTGCCCCTTGG[A/G]CAAAAGTAGAAGAGA | 13855 |
rs49030329 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556907 | GGACACACGTGCAAG[C/T]CATACATGGAGGTCA | 13855 |
rs49534804 | snp | G/T | | | missense | Epn2 | GRCm38.p3 | 11:61532574 | GTTCCACCCCAGGGG[G/T]TGGTCTGGTTAGCAG | 13855 |
rs49996961 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61578148 | AAAAGAAAAAAAAAA[A/C]CAAGACCTACAGGTG | 13855 |
rs50000297 | snp | A/G | | | downstream-variant-500B | Epn2 | Mm_Celera | 11:61516922 | CTGATGAACAGTGAT[A/G]TGGAAGCATAAATAA | 13855 |
rs50124091 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559160 | TGTTTACCTCTGAGG[A/G]ACTGCCAAAGTACTA | 13855 |
rs50365857 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61543005 | AACTCACCTGAGTCA[A/C]TGCCTAGGACAGAGG | 13855 |
rs50437757 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570775 | GCCGGGCGTGGTGGC[A/G]CAGGCCTTTAATCCC | 13855 |
rs50667439 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531699 | ATGTCACAATGCATG[A/G]GTCTCCCCCCGCCCC | 13855 |
rs50713391 | snp | A/C/G | | | utr-variant-3-prime | Epn2 | GRCm38.p3 | 11:61517839 | TGAGTCAACTCTGTG[A/C/G]GTGCTGGGGGCCAAA | 13855 |
rs51197897 | snp | C/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581067 | CTCTTCACAGCAATG[C/T]AAACCCTAAGACAAT | 13855 |
rs51480842 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570692 | ATTAAATACTAGGTT[A/T]AAAAAAAAAACTCAC | 13855 |
rs51506055 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567591 | AGTGTGGCTCTCTCG[A/C]GTTCAAGGCCAGCCT | 13855 |
rs51567564 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579186 | AAAGACGTGGGGAAG[A/G]GTATCCCCTTCCCCC | 13855 |
rs51569334 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61573797 | GGCTTAACAATTACG[A/G]GTACCATTTAATGAT | 13855 |
rs51775042 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539222 | CCAGCCAGCAGCAGG[C/T]TGCAGGACACTCCGC | 13855 |
rs51812189 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548693 | TACTGTATGCAGTAA[A/C]AGGTTGGGCCTCATA | 13855 |
rs51903601 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571768 | TACTTCTAAAAATCC[C/G]TGATTGGTCTGGGAA | 13855 |
rs52000360 | snp | A/G | | | downstream-variant-500B | Epn2 | Mm_Celera | 11:61516799 | CCCAGAGGGCTACCT[A/G]TAACAGTAGCTGGTA | 13855 |
rs52042390 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530053 | CACAAGTTGGGAAAT[A/G]TATGTGTGTCTGAGC | 13855 |
rs52284559 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536812 | TACACACACACGCGC[G/T]CGCGCGCGCGCTCGC | 13855 |
rs211709316 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61529937 | GGACACATAGCTGCT[A/G]AAGAGCTAGTGGCCC | 13855 |
rs211755517 | in-del | -/ACCT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570259 | TGGAGCTGCCCAGCC[-/ACCT]ACCTCTTCTGTCTTC | 13855 |
rs211870918 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61541808 | GGAGGAACACTGGCT[A/G]TACCTGAGCTGACAC | 13855 |
rs211924986 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572634 | AATCTCCAGACCCAC[A/G]CAAAAAGCTCAGCAC | 13855 |
rs212156803 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560804 | CTCTCAGGAGGATTA[A/T]GTAATATTGTCCTGA | 13855 |
rs212269990 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559269 | CTCTGGCCGTCCTGG[A/T]ACTCTGTAGACCAGG | 13855 |
rs212320828 | snp | C/T | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518344 | GTAAATGGAAGTCCC[C/T]GGCAATCCCTGCATT | 13855 |
rs212431069 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574224 | AATTTCTGAATACAA[A/G]GCCAGCCTGGTCTAC | 13855 |
rs212433692 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531678 | TCACCCTTCTACCTG[C/T]TGCCCATGTCACAAT | 13855 |
rs212481606 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548305 | CCTCTCCCTGGATTG[C/T]TGTGGTGTTTCTGTC | 13855 |
rs212556927 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567275 | GACAGAAGACACTGG[A/G]CACGTGGGATGTCTA | 13855 |
rs212569900 | snp | G/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581308 | TAACACAAGGTCATG[G/T]GGTCACTTTTCTTTT | 13855 |
rs212577676 | snp | G/T | | | intron-variant | Epn2 | Mm_Celera | 11:61520176 | CAGCTTCTCTAAAAC[G/T]TACTCAACCAAAAGG | 13855 |
rs212620981 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566034 | TTAAAATGATTACAG[A/G]GGTCAGCTATACTTT | 13855 |
rs212661750 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525210 | TTCTTTCCAATAAAT[C/T]AATATTCCTAAGTGG | 13855 |
rs212726111 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538840 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 13855 |
rs212788734 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61524470 | AGTAATGCCAGCACC[A/G]TTTCCACGCTGGTTC | 13855 |
rs212879446 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554847 | AGCACTCTCCTTATA[C/T]GGACTGCTCTGTAAA | 13855 |
rs212907844 | in-del | -/AA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570692 | ATTAAATACTAGGTT[-/AA]AAAAAAAAACTCACT | 13855 |
rs212963071 | in-del | -/AAAAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563229 | CCTGTTCCAAAAGAG[-/AAAAA]AAAAAAAAAAAAACA | 13855 |
rs213025899 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550193 | ATTGACAAAAAGCAC[-/T]TTTTTTTAGTAAAAT | 13855 |
rs213113870 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550105 | TGCTTTTTATTGTTT[-/G]GGGGTTTTGTTTGGT | 13855 |
rs213171168 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61557863 | CACAGGCTGTACAGC[C/T]AAGGCCCCACCAAGC | 13855 |
rs213181912 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571021 | AAGCAAGAGGATAAC[A/G]AATTTTAGGCCAACC | 13855 |
rs213281788 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537565 | CAGGCCCTGGCTTAT[A/T]TAGAGACACTCTAGC | 13855 |
rs213338088 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574916 | GGGTGAGAGCAGAAG[A/G]AGGATACAGCCTGCA | 13855 |
rs213451937 | snp | G/T | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518048 | TGAGTAGTGAGGACA[G/T]CAGGAGGTTGGGAGA | 13855 |
rs213529044 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563681 | GTTGTCCCTCCCTCA[A/G]TGAGACTCTCCTCTA | 13855 |
rs213538678 | snp | A/T | | | intron-variant, utr-variant-5-prime | Epn2 | GRCm38.p3 | 11:61578423 | AGAAATTCACCTTTT[A/T]CAATCATTTCAACCC | 13855 |
rs213538802 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562205 | ATACATACACAATTT[A/T]AAAACTCAGTATTAG | 13855 |
rs213585785 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576355 | GAAGCTTGTAGAATC[C/T]CGCACCTTCTTCTGG | 13855 |
rs213592702 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540871 | CTGCGCCCGGCCCGC[C/T]GCCTTACCCCCACCC | 13855 |
rs213613363 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61549576 | TGTCATGTGATTGAT[C/T]TGATATCCAGCAGTA | 13855 |
rs213753791 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539538 | ACCACTGTGACAGCG[-/T]TTTTTTATTTGAGGT | 13855 |
rs213763281 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525171 | TTCCACAATATACTC[-/T]TTAAAAAAAATCCTG | 13855 |
rs213803563 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536250 | CTGTAAACCTTTCTA[C/T]TTTACACAGTGAATG | 13855 |
rs213852319 | in-del | -/TTGT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553945 | CCACGTTTTGTTTTG[-/TTGT]TTGTGATTTTTTTCT | 13855 |
rs213898647 | snp | C/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580081 | AAGGAGGCCAGGTGC[C/T]AGACAGGGTTGATTT | 13855 |
rs214003109 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61523268 | TGCTTTTGCAGAACA[C/T]CAGGGTTTGGTTCCA | 13855 |
rs214253815 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61578688 | TTAGTTCCCCTAGTC[-/A]AAAAAACACAAGAAT | 13855 |
rs214311568 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61535390 | GGGAAGTAGCTGTGA[A/G]ATCGGGGGACAGGAG | 13855 |
rs214409449 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572235 | TATTCCCACCCACTG[-/A]CCTCAAATATCCTAT | 13855 |
rs214409542 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540661 | TTTTTGAGACAAGGT[C/T]TCATGTAGCACAAGT | 13855 |
rs214415192 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61528266 | AAATCATTGTACCAA[C/T]CTGAAGACAATAGAA | 13855 |
rs214445523 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550933 | CCCAGCAACCACAAG[A/G]TAGCCCCCAACCATC | 13855 |
rs214537655 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571203 | AATCCCCAGCACCCC[A/G]TGACAGCTAACTCCA | 13855 |
rs214546334 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567380 | TGGTAAATTTCTTCC[-/A]TAAATACTTTACAGT | 13855 |
rs214630235 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531641 | TCAGTCCCTGAATTA[C/T]GTGACACCCACTCCT | 13855 |
rs214694625 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530268 | TGGGGAGGGGACATT[G/T]CTGGGCTTTGGTGAT | 13855 |
rs214717158 | in-del | -/CACACT | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61557327 | GTGTATACATACACA[-/CACACT]CACACTCACATTCCA | 13855 |
rs214823228 | in-del | -/TA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539764 | ACGGTCATCCTTGGC[-/TA]TATACTGAGTTTGAG | 13855 |
rs214863846 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579992 | CAAGCACAGAACCCC[A/G]CCTAGCCTAATCAGA | 13855 |
rs214928911 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61578864 | CAATCTGCTCCCCCT[A/G]CAAAACCACTGGGCC | 13855 |
rs214929612 | in-del | -/A | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518530 | AGAGTTGAAGAAAGG[-/A]AAAAGGCAACTAGAG | 13855 |
rs214984617 | in-del | -/AAAA | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556308 | CTCGAAAAACAAAAC[-/AAAA]AAATAAATAAATAAA | 13855 |
rs215027250 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537289 | GAGCAGACATGCTGC[A/T]GCAATGAGGTCTCTC | 13855 |
rs215064760 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61523706 | TTGGGCCCTGCTCTC[A/G]AGTGGCTGAGTATCA | 13855 |
rs215085054 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536621 | CTTACATCTCCTGTC[C/T]TGAGCAGATAAGACA | 13855 |
rs215247990 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581615 | CAGTAAAGACTCAAA[A/G]GACCCAGAGAAAGCT | 13855 |
rs215306319 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564087 | ATCTGTCAGTACACA[A/G]ACATTTCCACCTCAG | 13855 |
rs215326651 | in-del | -/CTG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569138 | CAGTGCAGCCTCCAA[-/CTG]CTAAGTGTTCCCATT | 13855 |
rs215390182 | in-del | -/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61578166 | GACCTACAGGTGTTT[-/C]CCCCAACACAATCAT | 13855 |
rs215449100 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569854 | ACTGCTCTAAGTGTG[A/G]GCATTCTAGTCCCAT | 13855 |
rs215567627 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554066 | TCAAGAGATCCACCC[A/G]CCTTAGCATATGCAC | 13855 |
rs215689495 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560717 | ACTAACCCTCCATGC[C/G]CTCACTGAATATAAA | 13855 |
rs215750396 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530187 | ATACACTTTAACTTA[G/T]CAGGGTGCACAACCT | 13855 |
rs215757545 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61565751 | CTAACCAGGAAACTA[A/T]GACTGCTCTGAACCC | 13855 |
rs215836598 | in-del | -/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562950 | GTGAATACATCCACA[-/C]TACCACATCCTTAAC | 13855 |
rs215920042 | in-del | -/CTACCT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536841 | CGCGCACACACACAC[-/CTACCT]ACCTACCTACCTACC | 13855 |
rs215939520 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61532883 | GAAGCCAGGGATCCA[A/C]TACACCAAGGTCCTT | 13855 |
rs215942787 | in-del | -/TTT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558325 | GATATGGGAAAGTGG[-/TTT]TTTTTTTTTTTTATT | 13855 |
rs216105632 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547403 | AACTGAGGTACTGGG[G/T]GAGATGTCGTGATAA | 13855 |
rs216177820 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61552830 | ACAGATTCCTAATTG[A/G]GCCAAGGGAGGGTTT | 13855 |
rs216338374 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538890 | GGTGTGCACCACCAC[A/G]ACCGGCTGTTGTTTT | 13855 |
rs216382009 | snp | A/G | | | downstream-variant-500B | Epn2 | Mm_Celera | 11:61516780 | AAAACTGAAGGCCTT[A/G]GTGCCCAGAGGGCTA | 13855 |
rs216395731 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61555097 | AAGTGGCAGGGCCAG[C/T]GTGATCCCAGACCTC | 13855 |
rs216400308 | in-del | -/AAAT | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556311 | AAAAACAAAACAAAA[-/AAAT]AAATAAATAAATAAA | 13855 |
rs216498410 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554377 | CTAAACTGCTGCACT[A/G]CCCAAAGATAATCTG | 13855 |
rs216506920 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61555263 | CCTCTGCCTCCCACC[A/T]TGCCTGGCAGCTTTT | 13855 |
rs216525611 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560911 | ATATGGATATTGTTA[C/T]AGCTTTAAAAACAGC | 13855 |
rs216538916 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574289 | AAACCCCCCCCCCCA[A/C]AAAAAAGAAAAACAA | 13855 |
rs216656671 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61551048 | ACACTCAAACATATT[-/A]AAATAAAAACAGTAA | 13855 |
rs216878447 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61528704 | CCACCAGTCTGGATA[C/G]CTGCAACACTCCTCC | 13855 |
rs216904001 | in-del | -/AAATAAATAAATAAATAAAT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61549793 | GACAGGCCCTGTCTC[-/AAATAAATAAATAAATAAAT]AAATAAATAAATAAA | 13855 |
rs216934956 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542485 | ACCAGGCCCCTCATC[C/T]TCCAGTCAGTAAGGC | 13855 |
rs217001104 | in-del | -/TTTTTTTGTTTG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61555127 | CAGATTTCTAGTCTC[-/TTTTTTTGTTTG]TTTTTTTGTTTGGTT | 13855 |
rs217003076 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576193 | GTCAGTGCTCTTAAC[C/T]GCTGAGCCATCTCAC | 13855 |
rs217157866 | in-del | -/AGGG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525468 | TTTAGGAAGGAAGAC[-/AGGG]AGTCATGTGACCAAG | 13855 |
rs217198703 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61552715 | CCAAGCTACTGAAGG[C/T]TGTGCTGGCCCAGCA | 13855 |
rs217243300 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61551245 | ATTATTTGATTGACT[A/G]GGTATTCTTGTCTCA | 13855 |
rs217320335 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563776 | CTGGTGGGCCCACCT[A/G]TAGCCATGTACAAAC | 13855 |
rs217408796 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562163 | TCCAATGTTCAATGG[C/T]CTCTTCTGGACTCCA | 13855 |
rs217463936 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536330 | GACAAGTTAATTTCA[C/T]AGCTTGGGCTAATTG | 13855 |
rs217569758 | snp | G/T | | | missense | Epn2 | Mm_Celera | 11:61522409 | ATCTATATCTACCTG[G/T]TTTTTTTGAAGTTCG | 13855 |
rs217598515 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574288 | TAAACCCCCCCCCCC[A/C]AAAAAAAGAAAAACA | 13855 |
rs218030193 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558214 | CTCTTAACCACTGAA[C/T]CACCTCTTTAGCTGT | 13855 |
rs218041368 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579347 | GGAGGCAGACGTCGC[-/CT]CTCTCTCGGCTCCGA | 13855 |
rs218044195 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61557066 | CTGCACTAACTCACC[C/T]AGGCTAATCTCAAAT | 13855 |
rs218104769 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570748 | AATATTAAAGTTAAG[A/T]ACTCTTTAGTAGCCG | 13855 |
rs218120561 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571080 | AAAATAAAGCAGAGG[G/T]TCAATAAAAAAGAAT | 13855 |
rs218124513 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525950 | CAAGCACACTAAAGT[A/T]ACTACCACTGCCCTC | 13855 |
rs218168202 | in-del | -/TATACAGT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560844 | CAGGTCAGTCTAAGG[-/TATACAGT]TAGATCCTGTTTCAA | 13855 |
rs218201250 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570346 | ATTGGTTCTGCTCCT[C/T]CTCTATCCCCCGTAA | 13855 |
rs218334761 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542629 | AAAGAGTCAGCACAG[C/G]GACAGTATCTAGAAA | 13855 |
rs218335212 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61522893 | TCTTTCAACTGTGGG[C/T]ATACATAAGGGCCTG | 13855 |
rs218467288 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558959 | CAAAACAGTAAATGA[A/G]GACTCAATCACACCA | 13855 |
rs218565043 | in-del | -/AG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61557657 | CCCACACAAGACAAC[-/AG]ACTCAAGTGGGCACT | 13855 |
rs218568398 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560134 | AATAAATCTTTTTTT[-/A]AAAGGGGGGGGGGAT | 13855 |
rs218632768 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558021 | ACTAACTACCGCTTT[A/G]ATATTTGAGGGATTT | 13855 |
rs218652356 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61523850 | AAGGATGGCGCAGGG[C/T]TGGTGGGACAGGTCA | 13855 |
rs218668045 | in-del | -/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572360 | GGGGTGAGTTACTGT[-/C]ATAGAAATGACTTTA | 13855 |
rs218674507 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61578635 | GTGTCAAACACCCTA[C/T]CCCTAGATGACCTTG | 13855 |
rs218717635 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568829 | CATGTAGAAACAGGA[A/G]TGACTTTGGGTCAAG | 13855 |
rs218729202 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576742 | TGGCCAACAGTTTAT[A/G]CCAGAGCAAGATTAA | 13855 |
rs218732062 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567661 | AGAAAACCCTGTCTG[A/G]AGGAACAAAGAGTAA | 13855 |
rs218938507 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61535431 | TCATCCCATGCAAAG[A/G]CAGAACTGTCTCTCT | 13855 |
rs218978423 | snp | C/T | | | intron-variant, utr-variant-5-prime | Epn2 | GRCm38.p3 | 11:61555494 | ATCTTTGGGACACAG[C/T]GAGGGAGCGGGGCTG | 13855 |
rs219022884 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61565307 | ACCCAGGCCTCTGAG[A/G]GCTTGCTAACCCACT | 13855 |
rs219083790 | in-del | -/CA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571659 | CTTCTCTCTAGCTCC[-/CA]CATTCCCTTGCATCT | 13855 |
rs219087061 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559952 | GAGAGATGGCTCAGC[A/G]GTTAGAGCACCAACT | 13855 |
rs219145875 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571877 | CCATCAAATCCAAAC[C/T]CCTTAGCCACAAATC | 13855 |
rs219334499 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560968 | TACTTACCCCTAGCC[A/G]CCACCAGGTACCTCA | 13855 |
rs219423029 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567346 | CCATGCCTCTGTCCC[C/T]AGTCTAACATGATAG | 13855 |
rs219441669 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581440 | CCTGCTTTGCCATAA[A/G]AACTATAGTTCCATT | 13855 |
rs219658677 | snp | C/G | | | intron-variant | Epn2 | Mm_Celera | 11:61520956 | GAAAGAAGAGGAAGA[C/G]GTGCAAGCAGAGTGG | 13855 |
rs219729071 | snp | C/T | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518555 | CTAGAGGCTGCGGGG[C/T]TTGTTATTGTTGGAA | 13855 |
rs219755701 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61534692 | TAACGCATGCTTATT[-/A]AAAAAATAAGGTATA | 13855 |
rs219788397 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564358 | AAATATTTAATTCCC[C/T]TTTCTGAGCTCTAAA | 13855 |
rs219844482 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563048 | CACACCCCAAAAGAA[A/T]TAGAAAGGAATGAGA | 13855 |
rs219855304 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577745 | ACACTTTTTTTTTTT[A/T]AAGTTTCTCGTTTCT | 13855 |
rs219861676 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527563 | ACAGGATCTGCAAAG[G/T]GAGCTTCCCTCTCCC | 13855 |
rs219946649 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571401 | ACCCTTGATGGGGAT[A/G]ATAAGAACCGGCTCT | 13855 |
rs219990483 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61526314 | GGGTCTTTTCCTGGA[C/T]TGAATTCCCTATAGT | 13855 |
rs220000688 | in-del | -/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61532969 | TAGCTCTGGCATTGG[-/C]CCAGACCATGATTAC | 13855 |
rs220088077 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527781 | GCGCCTTCCTACTCT[A/C]TATATACCATGTTGG | 13855 |
rs220099820 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61524665 | CCTCCTCCCATAAGG[C/T]CTACGTCTTTCATCA | 13855 |
rs220147148 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570460 | CACGTTTTACATTGT[C/T]TATCTGCTGATACAC | 13855 |
rs220202710 | in-del | -/TTT | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518618 | TGTAATCAAATTCCG[-/TTT]TTTTTTTTTTTCCTA | 13855 |
rs220211687 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569081 | AGCCCCATCTAGAAA[A/T]GATGGCACCCACACT | 13855 |
rs220269786 | in-del | -/ACACACACAC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61573697 | GTTGTCCTCTGACCT[-/ACACACACAC]ACACACACACACACA | 13855 |
rs220384261 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61533394 | AGTGTCTTCCTCCTG[lengthTooLong]GTGTGTGTGTGTGTG | 13855 |
rs220399184 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61528881 | GAGCTGTCAAGTCTC[C/T]ATTCTGCAAGTAACA | 13855 |
rs220452871 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61534275 | AAGGGTAAGTCACTT[A/G]CAAAATCAGAGTCCT | 13855 |
rs220569296 | snp | A/G | | | downstream-variant-500B | Epn2 | Mm_Celera | 11:61516943 | GCATAAATAAACCCT[A/G]GCCTTCCCAAGTTGC | 13855 |
rs220670891 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61522786 | GGACATTGGGATGAG[C/T]CTGTGGGAAATGTCC | 13855 |
rs220686993 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61535730 | GGAGCCCAAGAGCCC[A/G]AAGGCTCCAATCAAA | 13855 |
rs220747307 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61521580 | CCCAGCCACAGGCCA[A/G]CAGTCCTTGAGAGGG | 13855 |
rs220753180 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61573255 | GGACTTCCTGCCATT[C/T]TGAAGTCCACTTTCA | 13855 |
rs220757222 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61535573 | ACAGTTGCACACCTA[A/G]AGGTGACACATAAAA | 13855 |
rs220768763 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61552026 | ATTCAAAACCTTAAA[C/G]AACCCAGACAAACAT | 13855 |
rs220867701 | snp | G/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580922 | AGCAACCACATGGTG[G/T]CTCACAACCATCTGT | 13855 |
rs220873911 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579325 | GCGAGGACAGGAGCC[A/G]AAGCCGGGAGGCAGA | 13855 |
rs220891964 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580977 | GTGTGTCTGAAGACA[A/G]CTACAGTATACTTAA | 13855 |
rs220971519 | snp | A/C | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580056 | AAAAATGTTGTGATG[A/C]AGAGACAGGAAGGAG | 13855 |
rs221053098 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536754 | AATAAAACTGCCTCC[A/T]ATCCACTTTGCTGAT | 13855 |
rs221068973 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553021 | GTCTACTTGTTAGAT[G/T]CTGTAACTGACACTG | 13855 |
rs221110407 | in-del | -/TG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525510 | CCACAGCCCTTAAAC[-/TG]TTTTTTTGTTGTTGT | 13855 |
rs221253556 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537994 | AGAGCAAGACACTCA[A/C]GGGTTCTTTGCTGAT | 13855 |
rs221271751 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536916 | GAATACTTAGGTCTC[C/T]ACTTTCTCATGCTCA | 13855 |
rs221306604 | in-del | -/AAAAAAAAG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563239 | AAGAGAAAAAAAAAA[-/AAAAAAAAG]AAACAAAATAAGAAA | 13855 |
rs221507877 | in-del | -/GAAGGAAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575842 | GAGGTAGGGAGGAAG[-/GAAGGAAA]GAAGGAAGGAAAGAC | 13855 |
rs221522578 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538051 | AGGAAGCCAGAGACA[A/T]GAGTTTACCAACTAG | 13855 |
rs221608846 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563503 | TAAATGTCCTATCCA[-/T]TTTTTTTTTCATTTA | 13855 |
rs221685031 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61545273 | TTTCTGTTATGTTGA[C/T]ATAATGTACTGTTCT | 13855 |
rs221698344 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542703 | ACTCCATCCAGACTC[C/T]ACCAGGCCCTCTCTA | 13855 |
rs221757743 | snp | C/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581676 | AAGAATGAGCCACCA[C/T]ACAGAGACATGATTA | 13855 |
rs221858696 | in-del | -/AAAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570691 | ATTAAATACTAGGTT[-/AAAA]AAAAAAAAAAACTCA | 13855 |
rs221957935 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531798 | ATGCTCAACTCACTA[C/T]TCTGATCTGACAAGT | 13855 |
rs221972671 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547822 | CCGAACCCCAGAGCT[A/G]AATCACAGGCTCCAG | 13855 |
rs221985032 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61526706 | GAGGAATAAAAGCAG[C/G]CTTCACTTCTCCCCA | 13855 |
rs221998858 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539495 | TCTAACCCAGAGCTG[C/T]ACTTTGCAGTCTCCC | 13855 |
rs222003883 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539702 | GTGGGTGGCACATGC[C/T]GGTGACCCCAGCTCT | 13855 |
rs222074823 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530844 | GTTTTGTTAAATATT[C/G]CAGTTTTGTTAAATA | 13855 |
rs222124732 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577216 | CCACAAGGCAGGAGA[A/G]CTCTGCACACAGTGG | 13855 |
rs222179110 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575787 | AAGGCCAACATGAGG[A/G]CTACATAGAGACCCT | 13855 |
rs222200098 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527599 | CATGGGGACAGAACA[C/T]GCAGTTGGCTTTCCA | 13855 |
rs222316932 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540952 | GACCTGGAATCTGTT[A/C]ATCTGTTTGCATGTC | 13855 |
rs222355683 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537719 | GAAAGCTCACATTTA[A/C]AGAGACCCAAGGAAA | 13855 |
rs222370059 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547944 | CCCATTCACAGTGAA[G/T]AGCCAGGATCCAACA | 13855 |
rs222379927 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61561054 | GGGCCTGAGAACTAC[A/G]GGGGGAAATGGCTAA | 13855 |
rs222459137 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530962 | CGTGTCCTACTCAGG[C/T]TCCCTGTCACAGCCT | 13855 |
rs222471690 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536862 | CCTACCTACCTACCT[A/T]TTGGTTGATTTTATT | 13855 |
rs222523251 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61545559 | ACACACAATCAGAAC[A/G]CAGATCAGTCCTGCA | 13855 |
rs222676090 | in-del | -/A | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61519210 | CTTAGGAAGAGACAC[-/A]GGGGCCCGACTAGGA | 13855 |
rs222693736 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61549729 | CAGACACAGCACTCA[C/G]GAGGCAGAGAATTAG | 13855 |
rs222774651 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61533132 | ATGACGGCAACATCT[A/G]TCATCAGGGCCCTGT | 13855 |
rs222825123 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550142 | TTTTTTTTTTCTTGG[C/T]TTTTTTGTTTTTAAA | 13855 |
rs222846062 | in-del | -/TTTATCAAGACAGCAG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572764 | GCTAAGGAGGGACCC[-/TTTATCAAGACAGCAG]TTTATCAAGACAAAG | 13855 |
rs222982245 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61555804 | GCCACCACTGGAAAG[A/G]CTCTGCCTCTCTTTA | 13855 |
rs223113552 | in-del | -/CT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563265 | AGAAAGGACCCACAC[-/CT]GTATGCTATACTACC | 13855 |
rs223218111 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542528 | CTCTGCCAACCTCCA[A/G]CCAGAGGAATTCTCC | 13855 |
rs223515669 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61541005 | CAGACAATCTACAAG[A/G]CTGCAGGGTTACAGA | 13855 |
rs223599048 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556804 | GTCAAAGCAGGACCT[A/G]CTTCCCTACCCACTT | 13855 |
rs223702360 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553174 | GCAGCCTGGGAAAAT[A/C]TCAAGTTCCCACGAT | 13855 |
rs223702496 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558844 | GTACACACCTGTAAT[C/T]CCAGTACTCAGGAGG | 13855 |
rs223714109 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61552281 | GCTGACAGGTGCCAC[A/G]CAGCCTCCTTTGATT | 13855 |
rs223783000 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61549880 | TCTGAAAATGACTAT[G/T]ATTATAACCACAAAA | 13855 |
rs223866763 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562735 | CCACATGCGTATTAC[G/T]CAGCATATGCCTGCC | 13855 |
rs223894190 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554878 | GGTATTGGCTCCCAG[C/G]GACAGTACCAGAACT | 13855 |
rs223950607 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568384 | AGCCTGGGAACTGAA[C/G]AAAGCAGACCCCACC | 13855 |
rs224019919 | snp | A/C | | | intron-variant | Epn2 | Mm_Celera | 11:61521645 | GCAACTGCTAAAACG[A/C]AGCACATGCCTACCT | 13855 |
rs224064507 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61519877 | ACTGGCAAACATCTA[C/T]AGACTGCTAAAGCCA | 13855 |
rs224117994 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539906 | TTTGAACCCCAAAAC[C/T]CACATGATGACTCAC | 13855 |
rs224146426 | snp | C/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61555883 | GGTCTCAGTCAATCA[C/G]AGAGACTCCAAAAAT | 13855 |
rs224195563 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61565161 | AACCCAGCCTTAATC[C/T]TCCCGCCCTGCAACT | 13855 |
rs224262364 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563695 | AATGAGACTCTCCTC[C/T]AAGCCCTTCCAGTTT | 13855 |
rs224269558 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566471 | GTGCTCCAACTCCAT[A/G]GGTGGAATGAGTCCC | 13855 |
rs224471632 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553679 | GTCAGGCCTGAAGGG[C/T]CTGAAAGTAGCTCCT | 13855 |
rs224533707 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567589 | TCAGTGTGGCTCTCT[C/T]GAGTTCAAGGCCAGC | 13855 |
rs224540845 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61552649 | GTTATTAAAATCATG[C/T]GAAAAGGCATACCAT | 13855 |
rs224544136 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566569 | ATTGCTGCCAAGTAA[C/T]CCCTCTAAGAAAGCA | 13855 |
rs224630849 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553422 | ATTGTTTGGCCCCCT[A/G]ATGCACTTCTTGGGG | 13855 |
rs224633394 | in-del | -/AG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564859 | AAAAAAAAAAAAAAA[-/AG]GCAATAGGCTAAGTA | 13855 |
rs224816141 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540035 | TTTAAAACACACATT[-/A]AAAAAATAAAAGCAT | 13855 |
rs224919979 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558388 | CCTAAAACATACAAT[C/T]AAGTTTTGTTTCTAG | 13855 |
rs224975666 | in-del | -/TT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61544759 | GATGGGCCAATCTTA[-/TT]TTTTTTTAATTAATT | 13855 |
rs225047181 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559693 | GGCTTCGGAGGAAGC[A/G]GAAACTTAGTTTTCA | 13855 |
rs225068078 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570861 | TAGAGTGAGTTCCAG[A/G]ACAGCCAGGGCTACA | 13855 |
rs225077638 | snp | C/T | | | downstream-variant-500B | Epn2 | Mm_Celera | 11:61517027 | GTGAATGTGAAACCA[C/T]TAAAGCATGCTGAGA | 13855 |
rs225128631 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572658 | TCAGCACAGAGCACA[C/T]GCCTATAACCCCACA | 13855 |
rs225222529 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61561132 | CTCATCTTTTTCGTC[A/C]CACTGGCCCCTTGAA | 13855 |
rs225414987 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61528578 | TGAAATAAATCTTTA[C/T]AGATAAAGTTTCTCA | 13855 |
rs225625943 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550109 | TTTTATTGTTTGGGG[-/G]TTTTGTTTGGTTTGT | 13855 |
rs225711807 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61529765 | GGCTCTTAGCCACTC[A/G]GTTTTAGCAGAGGCT | 13855 |
rs225818065 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560777 | GTTTGTGCACATCTA[A/T]AATTCTATCATCTCT | 13855 |
rs225827948 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61523974 | AACACACACCCAACA[C/T]GCACTCACATACACA | 13855 |
rs225875256 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558324 | ATGATATGGGAAAGT[-/G]GTTTTTTTTTTTTAT | 13855 |
rs225912245 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569059 | CTACACAGAACTGGC[A/G]CCCACAAGCCCCATC | 13855 |
rs226017435 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567915 | GAATAATCCATGGGA[A/G]TAACCTAGATTTAAA | 13855 |
rs226164367 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527022 | TCACACTACAGGGGT[A/G]GTACTTCATCAGGCA | 13855 |
rs226169479 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575958 | TCCCAGCAACCACGG[G/T]GGCTCACAACCATCT | 13855 |
rs226228144 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525151 | AATTGGTTCTGACAG[A/G]GGAATTTCCACAATA | 13855 |
rs226264287 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556508 | ATGCATGCATGTGGT[C/T]GTGTGGTGTGTGTCT | 13855 |
rs226288718 | in-del | -/GTTTG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547175 | CTTTTTGTTTTGTTT[-/GTTTG]TTTGTTTGTTTGTTT | 13855 |
rs226289403 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581260 | TAGAGTCCTTTTCTC[A/G]GCCCACGATATATTA | 13855 |
rs226368073 | in-del | -/CTG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531841 | CTGGTTCACACAGCA[-/CTG]CTCGCTGCTACCAGG | 13855 |
rs226392437 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569869 | GGCATTCTAGTCCCA[A/T]AGGACCATGCATGTC | 13855 |
rs226498180 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568078 | GCTGTCAGATACAAA[A/G]AGCTCTAACAAGTGT | 13855 |
rs226540543 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61532149 | AATTCTGCCAAGTTC[A/C]TGTTTTAAATCAGAC | 13855 |
rs226559452 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566962 | TGCGTCCTTAAGTCC[A/C]TCCAAAATGTGTTGT | 13855 |
rs226600214 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531530 | AACACTAATTGGCCC[C/T]AGGAAGTTGGCAAGC | 13855 |
rs226684072 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61526855 | TTCTGGTTCTAATGC[C/T]CCAGAACCACTAGGC | 13855 |
rs226702015 | in-del | -/TTCAGAACAGGGGC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61523215 | AAGTCAGAGTCAAAA[-/TTCAGAACAGGGGC]TAGAGAGTATTAAAG | 13855 |
rs226706176 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531902 | AGATAATTCATATGG[C/G]AGGACAGAGCCTAGC | 13855 |
rs226762119 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576254 | GAGATACAGAAAATA[A/C]ATTTGAGGGTTTGAG | 13855 |
rs226836922 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575460 | CAAATCTAAGAGTTT[C/T]CACTCACATACAGGT | 13855 |
rs226934703 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61522695 | GGGATAAGAGAACAC[A/G]AGTGCCTCCCACTGC | 13855 |
rs226995281 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61521206 | GAAATGAGGTAAGAG[A/G]TCAGAGGTCAGAGGC | 13855 |
rs227011973 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61533254 | AGCAAAGTAAGGGGG[A/G]TAGGGGATGGGGTGA | 13855 |
rs227035907 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566277 | AATAGTCAAGGCCAT[A/T]TGGAGAAACCCTGTC | 13855 |
rs227110935 | snp | A/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580539 | GGGGAGAGTACAGGG[A/T]ACTATTTCAGTTGTT | 13855 |
rs227229894 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579188 | AGACGTGGGGAAGAG[C/T]ATCCCCTTCCCCCGG | 13855 |
rs227392892 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61535156 | AAGACATAAACTCAT[C/T]AAGTAAGTGCCTTAA | 13855 |
rs227476662 | in-del | -/T | | | intron-variant | Epn2 | Mm_Celera | 11:61521056 | TAAGCTCAGAAGGAC[-/T]TTACTGACAGCATCT | 13855 |
rs227497018 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527120 | AGCCAGAAAAGCTGG[A/T]ATGATGACACACAGA | 13855 |
rs227512457 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540171 | AGAGAACCTGAGACT[C/T]CAGAAGTGGATGTGA | 13855 |
rs227583444 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564715 | GAAATGACTAGGCAC[A/G]ACATGTCATGGAGAG | 13855 |
rs227589918 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61524046 | GTTAACCCCGTGTGT[A/G]GATTTTTCAATTACC | 13855 |
rs227606843 | in-del | -/A | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581005 | TAAATAGAATAAATC[-/A]ATAAATCTTAAAAAA | 13855 |
rs227680111 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61523237 | CAGGGGCTAGAGAGT[A/G]TTAAAGAGTTTCTAC | 13855 |
rs227689119 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61578138 | AACATTCAAAAAAAG[-/A]AAAAAAAAACCAAGA | 13855 |
rs227708227 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536161 | TCAGCACACCCTCCT[C/T]CCCCTGTTCACCAAC | 13855 |
rs227806071 | snp | C/T | | | synonymous-codon | Epn2 | GRCm38.p3 | 11:61546250 | ACGGCCAAAGGTGAT[C/T]TGGTTGCTGCCCACG | 13855 |
rs227806299 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540282 | ACCACAAGCCCAGCA[C/T]TGCTTGAGACTCAGG | 13855 |
rs227861662 | in-del | -/TT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547172 | TATCTTTTTGTTTTG[-/TT]TTTTTTGTTTGTTTG | 13855 |
rs227877558 | snp | C/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581416 | ATGAATGAAATCACA[C/T]GTTATGTACCTGCTT | 13855 |
rs227961732 | in-del | -/AC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576404 | CATGTACACATAGAA[-/AC]ACACAAAAATAATAA | 13855 |
rs227971706 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61541146 | GTAAAAAACACCGGG[C/T]TCTCTTGTACCTCCT | 13855 |
rs228049734 | in-del | -/TAAG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572197 | TCCTCTCAGTCAGAC[-/TAAG]TGTGTCAGCAAGAAA | 13855 |
rs228072413 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538881 | GGGATTAAAGGTGTG[C/T]ACCACCACGACCGGC | 13855 |
rs228077563 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571035 | CGAATTTTAGGCCAA[C/T]CTAAACTATACATAG | 13855 |
rs228285884 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61573792 | GGGATGGCTTAACAA[C/T]TACGGGTACCATTTA | 13855 |
rs228504779 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61528043 | ATATTTAGTGGGTCT[A/G]TTTTGAGATAAATAG | 13855 |
rs228508848 | in-del | -/TGG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536573 | ACGTGGAATCATTCA[-/TGG]TGGTGGTGGTGGTGG | 13855 |
rs228535534 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538407 | TGTTTCAAAACAAAA[A/C]CTGAACAGATGAGCA | 13855 |
rs228543276 | in-del | -/AAAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531979 | AAGGTCCACTTTATG[-/AAAA]AAAAAAAAAAAAAAA | 13855 |
rs228620540 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554706 | CAGAGACACATGCAT[A/G]TCACAGGAGATAGAA | 13855 |
rs228622453 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537241 | GCCATGAAGTCACAG[A/G]AGATCCACCAGGTCA | 13855 |
rs228672518 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572058 | CAGCTCAACCCTACC[G/T]CTCCCTGATATCCTC | 13855 |
rs228748796 | in-del | -/ACC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61533280 | GGTGAGGGGATGAAG[-/ACC]AGTATAACCAATGGC | 13855 |
rs228939492 | in-del | -/TC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542570 | AGTGCTTCTGAGGTT[-/TC]TAAGCTTTTTTATCC | 13855 |
rs228939706 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61546041 | ATCTAGATCGAGGAC[A/G]CTGTCGCCTGGGTCT | 13855 |
rs228992888 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560333 | AAAATAAAAAGAAGA[A/C]GACGACAACAACGAC | 13855 |
rs229143113 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61578576 | TGGGGGAATCCTAAA[C/T]GTTGAAGAAATCCTT | 13855 |
rs229196621 | in-del | -/CACACACGCGCGCGCGCGCGCGCTCGCGCG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536801 | CTTTAAAAATATACA[lengthTooLong]CACACACACACACCT | 13855 |
rs229275825 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61523289 | TTTGGTTCCAAGCAC[C/T]CACAACAGCATTCTC | 13855 |
rs229276849 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548587 | CCCATCTGTTCAGCT[C/T]TCATGAATCCCCAAA | 13855 |
rs229295518 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574041 | ATAGCTAACCCACTC[A/G]GAAGGCAGAAGCAGG | 13855 |
rs229323608 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536292 | TGGATGGATGGGTGG[A/G]TAAGTGGGTAGACAA | 13855 |
rs229332861 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562042 | CTGGAGAGACGGCTC[A/T]GCAGTTAGGAACACT | 13855 |
rs229340283 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61524128 | AAACACTGCTTCATT[C/T]CCAGATCCACCGCAA | 13855 |
rs229385976 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538008 | ACGGGTTCTTTGCTG[A/G]TCTGTAAACACCAAC | 13855 |
rs229465599 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536033 | GAGCCTGGGTGTATA[C/T]CCACCTCTGCACACT | 13855 |
rs229476800 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61534998 | AAGCTGGAAGCACAC[A/G]GCTCCCTCAGAAGTC | 13855 |
rs229527579 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61557377 | AACGCCTCAGTTACT[C/T]CCATATCTCTATTGT | 13855 |
rs229532594 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550463 | GGGCCTCAAAAGCCC[A/G]GCTCATCCATACTAG | 13855 |
rs229593248 | snp | A/T | | | intron-variant | Epn2 | Mm_Celera | 11:61524885 | TTTTCTCCCCTCAAA[A/T]CAGAGTCTCACATAC | 13855 |
rs229706150 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554353 | CTCTCCCCACTCAAT[A/G]TGGCCCCTCTAAACT | 13855 |
rs229717422 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553103 | CTCCACCTAGGGGCA[A/G]GCTGTAGATGACAGT | 13855 |
rs229718935 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567277 | CAGAAGACACTGGGC[A/C]CGTGGGATGTCTAAC | 13855 |
rs229757826 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566222 | GGAGCAGAGGCAGTC[C/T]GTGAGTTTGAGGCCA | 13855 |
rs229874107 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558483 | ATCCTTCTCAAATCC[C/T]CCATATCAATTAGTA | 13855 |
rs230226455 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542255 | TGCAAAGCTGGAAGC[A/G]CTGGAACAGAACTGC | 13855 |
rs230286884 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540897 | CACCCCCCTCACTCC[C/T]GCTGTGGAGAAAACC | 13855 |
rs230288935 | in-del | -/AA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566768 | CCATTGGATCCCATG[-/AA]AACACAAGTTTGTCT | 13855 |
rs230288959 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558008 | CTTAGGAATGAAAAC[C/T]AACTACCGCTTTGAT | 13855 |
rs230343235 | in-del | -/TTTTGTTTG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61555130 | ATTTCTAGTCTCTTT[-/TTTTGTTTG]TTTTTTTGTTTGGTT | 13855 |
rs230343261 | in-del | -/ACG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570946 | CTTACTTTTAAAAAC[-/ACG]ATGATTTTGCTGAGC | 13855 |
rs230349467 | snp | C/T | | | intron-variant, utr-variant-5-prime | Epn2 | GRCm38.p3 | 11:61555531 | CAGAGGTCTTGAGTT[C/T]TATTCTCAGCAACCA | 13855 |
rs230423323 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61546958 | AGAAGCACTGGTGAG[A/G]ATGGGAGAGCCCAAG | 13855 |
rs230450595 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575140 | CTTAAATGCAGTACA[C/T]TGCTTGAACTAGGAT | 13855 |
rs230600904 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548226 | TGGCTGGCTACTGTA[A/T]CAGGCTGAGACCCTC | 13855 |
rs230689268 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525735 | TTAAACTACAGTCAA[-/G]ATCTAGTGTGAAAAA | 13855 |
rs230712226 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576536 | GGCATTCCATGGCAA[C/T]CAGAGCTCCACAGCC | 13855 |
rs230713439 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560980 | GCCACCACCAGGTAC[C/T]TCATCTATAAAATGT | 13855 |
rs230769438 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538822 | TTGTCGACCAGACTG[A/G]CCTCGAACTCAGAAA | 13855 |
rs230827520 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554812 | AGCCTGGAGATGCGA[C/T]CTCTCCTTCCAGACC | 13855 |
rs230840492 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61521200 | AGAGTAGAAATGAGG[C/T]AAGAGATCAGAGGTC | 13855 |
rs231061377 | in-del | -/AAAACAAAAAAC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570897 | AAACCCTGTCCAAAA[-/AAAACAAAAAAC]AAAAAAAACCTCTTT | 13855 |
rs231095891 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554087 | GCATATGCACAACCA[C/T]GCCCAGCATCGCTTG | 13855 |
rs231120687 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566690 | CAAGAAAACAGACTT[-/A]AAACTTTGTGGGCTA | 13855 |
rs231344377 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539952 | CGGTCTGAGGGGATC[G/T]GATGTTTCTGACCTC | 13855 |
rs231350706 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558596 | GGCAATATATAGCCC[-/T]TTTTTTTTGTTTTGT | 13855 |
rs231398123 | snp | A/T | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518029 | TTAATACTTTTCTTA[A/T]CAGTGAGTAGTGAGG | 13855 |
rs231421742 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548100 | AGAGAAAACAAGGGC[C/T]CTCGGCAGCCCTGCT | 13855 |
rs231528887 | in-del | -/AAAAAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61578129 | CAAAAGCAAACATTC[-/AAAAAA]AAAAAAAGAAAAAAA | 13855 |
rs231622036 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61561053 | GGGCCTGAGAACTAC[-/G]GGGGGGAAATGGCTA | 13855 |
rs231764383 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564835 | CTCTTCTCCAGACTT[C/T]TGCTTTAAAAAAAAA | 13855 |
rs231823115 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566303 | TGTCTTGGGGGGAGG[-/A]AAAAAAGACTCTGAA | 13855 |
rs231891137 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559216 | TGTTGTTGTTTGCAC[A/G]CTGTTGTTGCTTCTC | 13855 |
rs231904907 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558130 | GAGAGGACATCAGGT[C/T]GTCTGGAAATACAGT | 13855 |
rs231907481 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572497 | CACAAAAACACACAG[A/C]ACACCTCAGGGTAAA | 13855 |
rs232000608 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571345 | AATTTTGCAAAATTT[A/G]CCTGCTGAAATGATT | 13855 |
rs232008352 | snp | G/T | | | intron-variant | Epn2 | Mm_Celera | 11:61524209 | TATGCTGGATAGCTA[G/T]GCCAGATTTCTGAAT | 13855 |
rs232022785 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61523821 | CAACTTAGTGTGTCA[C/T]AACTGCCTCTCACAA | 13855 |
rs232083193 | in-del | -/AGAAAATAC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576684 | CCAACACTGCCGGGA[-/AGAAAATAC]AGAAATCCACTAGAT | 13855 |
rs232127344 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556011 | GCTTTTAAGATATAT[A/G]GATATTTGTTTTCCT | 13855 |
rs232138089 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569828 | ATTCTCCAGGGATTT[C/T]TAGAAAACACACTGC | 13855 |
rs232224322 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581616 | AGTAAAGACTCAAAA[A/G]ACCCAGAGAAAGCTG | 13855 |
rs232483204 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567590 | CAGTGTGGCTCTCTC[A/G]AGTTCAAGGCCAGCC | 13855 |
rs232511015 | snp | C/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580037 | GTATTTCCTCTTGCA[C/T]GTGAAAAATGTTGTG | 13855 |
rs232524441 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61578870 | GCTCCCCCTGCAAAA[C/T]CACTGGGCCAACTTC | 13855 |
rs232526075 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576442 | GCAATAAAATAAATC[-/T]TTTTTTTTTTAATTA | 13855 |
rs232687340 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558991 | ATCAGTGAGCCGCTC[C/T]ATTTCATGGCTAAAT | 13855 |
rs232689599 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61557268 | GGTACAGCTCAATCA[C/T]CTTTTAGGAAGTAAT | 13855 |
rs232719084 | in-del | -/TT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575241 | CTCAAAGAGGCATGC[-/TT]TTTTTTCCCCCCCTT | 13855 |
rs232739926 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572301 | CCCTGCACCTTTTGG[C/T]TCCTACTCAGAGGTA | 13855 |
rs232753217 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570774 | AGCCGGGCGTGGTGG[C/T]GCAGGCCTTTAATCC | 13855 |
rs232796702 | in-del | -/TTC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563453 | GTATTTTAATAACCT[-/TTC]ATTTTAGAACTGAGC | 13855 |
rs232829950 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574526 | TTCAAGCCACCCTAA[A/G]CTACACAAGAACCTA | 13855 |
rs232839829 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572718 | AGTTCACTGACCAGA[C/T]AGCCTAGCCAAATGA | 13855 |
rs233051973 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581124 | TTTCATTCTGCCTTT[A/G]CTCACTGAAGGAGAG | 13855 |
rs233082454 | in-del | -/ACTGTTA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568422 | CAATAGCATCCTGAC[-/ACTGTTA]AGTGCCCATTCTCCT | 13855 |
rs233178167 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61524979 | TAGTTTTCCTATTTC[A/G]GTTATCTGAGACAGG | 13855 |
rs233462297 | in-del | -/AC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61533506 | CCTGTTGTGTGTCCT[-/AC]ACCCTCACTGTAGTC | 13855 |
rs233494501 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560482 | CCTGGGCAAAGGATT[A/G]AGAGGCCCAGGAACT | 13855 |
rs233774911 | snp | C/T | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61519058 | GTGGGGCCAGAGCTT[C/T]ACCTTGTCCACACCC | 13855 |
rs233799926 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530207 | GTGCACAACCTCCCA[A/G]CAATCTAAGATGTCC | 13855 |
rs233856324 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61528711 | TCTGGATACCTGCAA[C/T]ACTCCTCCTGAGCCA | 13855 |
rs233856366 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61543345 | CCAGGGCTCAATAGA[A/G]GTTGGCTACCTTATC | 13855 |
rs233869253 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542499 | CCTCCAGTCAGTAAG[A/G]CCTCCTAGTCCAGCT | 13855 |
rs233896771 | in-del | -/AGGA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575836 | AGAAAGGAGGTAGGG[-/AGGA]AGGAAGGAAGGAAGG | 13855 |
rs233908577 | in-del | -/ACAC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61573698 | GTTGTCCTCTGACCT[-/ACAC]ACACACACACACACA | 13855 |
rs233922698 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563178 | GAGGCAAATGTATCT[C/T]TACGAGTTTGAGGCA | 13855 |
rs233981370 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577945 | GCCACACAGTTACAC[A/C]TAACTAGCCTAACTT | 13855 |
rs233996539 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61565317 | CTGAGAGCTTGCTAA[C/T]CCACTACAGAGGAAT | 13855 |
rs234028922 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61573561 | ATGCAGACACTGGTT[-/A]AAAAACGTATGTTCT | 13855 |
rs234074210 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Epn2 | GRCm38.p3 | 11:61579712 | GGCAGCGAGCGCGCG[C/T]GCGCGAGCCCCGCCC | 13855 |
rs234092196 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531749 | ACACACTATTCTACA[A/T]GACACTGTTTCTCAG | 13855 |
rs234156459 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536369 | GTTCTAATCTATACT[A/T]AGAACTTCCTTCTTT | 13855 |
rs234171612 | snp | A/C | | | intron-variant | Epn2 | Mm_Celera | 11:61524142 | TTCCAGATCCACCGC[A/C]AAGTGTCCTGAGCCC | 13855 |
rs234225968 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61535458 | CTCTTATTCCTAGTA[C/T]AAGATAGTACTCAGT | 13855 |
rs234226301 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61552720 | CTACTGAAGGCTGTG[C/T]TGGCCCAGCAGCTAC | 13855 |
rs234237646 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61551327 | TTCATCTTTCTAAAA[A/G]AAGCTAACAGCCTGT | 13855 |
rs234305962 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537566 | AGGCCCTGGCTTATT[G/T]AGAGACACTCTAGCC | 13855 |
rs234321957 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558044 | GGGATTTAGGATTTC[-/T]TTTTTGTGTAAAAGA | 13855 |
rs234340813 | snp | G/T | | | intron-variant | Epn2 | Mm_Celera | 11:61522496 | GCTCAAAGGACCCTG[G/T]GGGGACATACAAGCT | 13855 |
rs234431902 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61526059 | CATTCTTCAGCTTCC[A/T]GAACAGTAACTTTTA | 13855 |
rs234496527 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539093 | AAGTCAGTCTTATAT[C/T]AGTGAAGGGAAAGGT | 13855 |
rs234512710 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537720 | AAAGCTCACATTTAC[A/C]GAGACCCAAGGAAAA | 13855 |
rs234572205 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554556 | CAGTTCTTCCCACCA[C/T]AGAACCACATCTTGC | 13855 |
rs234583006 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531351 | GCATCAGCTCTCATT[A/T]TGGGTGGTTGTGAGC | 13855 |
rs234722039 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527354 | CAGAAGACTGCTGTC[A/G]TCTTTCTTCTTGCCC | 13855 |
rs234747853 | snp | C/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581545 | CAAAAGACTAGTTAA[C/T]AGGAGTGGGCAAAAT | 13855 |
rs234782071 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568835 | GAAACAGGAGTGACT[C/T]TGGGTCAAGAGTCTG | 13855 |
rs234984530 | snp | C/G | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61517715 | CGGCCTCTGGTCCTG[C/G]GTGGAATGGGTAGTT | 13855 |
rs235103390 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576159 | GCTGGGATTTGAACT[C/T]GGAACCTTTGGAAGA | 13855 |
rs235244490 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61522298 | CACACACACAGGCAC[A/G]CACACAAACATGCAT | 13855 |
rs235334872 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550977 | CCAGGGGCTCAGATA[C/T]CCATTTCTGGCATCT | 13855 |
rs235561592 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61535393 | AAGTAGCTGTGAGAT[C/T]GGGGGACAGGAGGGG | 13855 |
rs235590023 | in-del | -/AGCTCTAGG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61543042 | AGAAGAGCTCCATGA[-/AGCTCTAGG]AGAACCTGAGAACAG | 13855 |
rs235696973 | snp | C/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580331 | AAAGCAATGTAGGGC[C/T]GGCCACATGCCAAGC | 13855 |
rs235918189 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536806 | AAAATATACACACAC[A/G]CGCGCGCGCGCGCGC | 13855 |
rs235976566 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554650 | AGCTGAACGGAACTG[A/G]TAAATGACAGGTATC | 13855 |
rs236030270 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567766 | GTCACAGGCAAACCT[A/G]AGTTACAGAATAAGA | 13855 |
rs236032461 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553788 | CCTCCCTGCCAGAAA[A/G]GCTCTTGCCTAGAGC | 13855 |
rs236070998 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525372 | AATTTACCTATAAAG[C/T]TCTCTGGGTGGACTT | 13855 |
rs236105472 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564378 | TGAGCTCTAAACTGA[-/T]TTTTTTTCCTTCTAA | 13855 |
rs236321554 | in-del | -/TCCC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563902 | CTTACCTAGCACCCA[-/TCCC]TATCAGGCCTGGACA | 13855 |
rs236385527 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559974 | GCACCAACTGCTCTT[C/T]CAGAGGTCCTGAGTT | 13855 |
rs236450361 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558567 | TCTTTATGGATTTCT[C/T]TATATATGGAATCAG | 13855 |
rs236450419 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61573053 | AACTCTAAACACCAA[A/C]GAATATTAAATCAAT | 13855 |
rs236463214 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571944 | ATCGAGATGTATACA[C/G]AAGAGCATCCACACC | 13855 |
rs236464700 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531650 | GAATTATGTGACACC[C/T]ACTCCTTTCCCCTCA | 13855 |
rs236506451 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547239 | TTTAGCCCTGGCTGT[C/T]CTGGAACTCACTTTG | 13855 |
rs236520772 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560820 | GTAATATTGTCCTGA[A/G]TGTGAGGCCAGGTCA | 13855 |
rs236585236 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559295 | CCAGGTTGAATGATC[C/T]GCCTACCTCTGCTTT | 13855 |
rs236700054 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61565951 | TACCACAATCTTGAA[C/T]ACAGAGTTCATACCC | 13855 |
rs236737357 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570252 | TTGTTGCTGGAGCTG[C/T]CCAGCCACCTACCTC | 13855 |
rs236743173 | in-del | -/GAACTC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577275 | GCTTCAGTCCACAAA[-/GAACTC]GAAAGTTGCCACTAT | 13855 |
rs236984203 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61552138 | AGCTATATCAGCATG[A/G]AGACTGAGAGCTGCC | 13855 |
rs236995889 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61552898 | TCATTCCTCAATGCC[A/G]TTCTAGGCTACAAAG | 13855 |
rs237323824 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61555392 | AATCCCAGCAACCAC[A/T]TGGTGGCTCACAACC | 13855 |
rs237402085 | in-del | -/ACGCCT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536074 | ATAAACTGCAGATGG[-/ACGCCT]ACCCATGGAAGGAGC | 13855 |
rs237532558 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579182 | CGAGAAAGACGTGGG[A/G]AAGAGTATCCCCTTC | 13855 |
rs237695493 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527796 | CTATATACCATGTTG[C/G]CATCAGGACTAGAGG | 13855 |
rs237707952 | in-del | -/AG | | | intron-variant | Epn2 | Mm_Celera | 11:61522257 | CCCGCTGGAGATGAC[-/AG]GGGGGAAAAATACAT | 13855 |
rs237806247 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556119 | GTGAGGACCTGAAGT[C/T]CCCATGCTTCCTGTG | 13855 |
rs237912193 | snp | A/G | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518923 | CAAGCACAGAGCCAC[A/G]GGGCAGGGTTGCGCT | 13855 |
rs238079600 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562182 | TTCTGGACTCCACAG[A/G]CACACATATACATAC | 13855 |
rs238095889 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61534395 | CCTCCTGGGCACCTT[A/G]ATCCTGTGGAGCCAT | 13855 |
rs238112594 | in-del | -/AT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550752 | TGATATCCCATAGAC[-/AT]ATGTCCTTAAGACTT | 13855 |
rs238133489 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61544464 | GTGCCCTGTGCCTGG[A/T]GGTCATGAAGAGCCT | 13855 |
rs238370947 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61535582 | CACCTAGAGGTGACA[A/C]ATAAAACCTTGGCTG | 13855 |
rs238370973 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61521585 | CCACAGGCCAGCAGT[C/T]CTTGAGAGGGGAAAA | 13855 |
rs238378008 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564539 | TGGGGGAGATCAAAG[A/T]ATCTACACATCTGCA | 13855 |
rs238378146 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550331 | CTGGACTGCTCAGTT[A/G]TATGAAATACCTGTA | 13855 |
rs238437604 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563112 | CATAAAAAGAGAGGG[G/T]AAGAGCTGAGCTTAG | 13855 |
rs238546357 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580936 | GGCTCACAACCATCT[A/G]TAATGAGATCCGGTG | 13855 |
rs238556426 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579458 | CGGCGAGGGGGAAGC[C/T]GGTGCTCTTAGGGGC | 13855 |
rs238644662 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61526796 | GAGCACTTCCAAATG[-/T]GCACTTTTCCTGTTC | 13855 |
rs238658904 | in-del | -/CT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61529408 | CAGTCCTGGCCTTGG[-/CT]CTGGTAGGTGGGTAG | 13855 |
rs238736223 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537417 | TGCAAAGCCGAATGT[-/G]GGAACTTCAAGACAA | 13855 |
rs238756574 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570550 | GCAGGCAGAGACTTA[A/C]ATTTTACTCACTAAC | 13855 |
rs238785827 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556698 | TCTACTATGTATGCT[A/G]GATATAGAAAGGTTA | 13855 |
rs238818200 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564164 | TAAGGCTCAAAGATT[A/G]GAAAGTCATCAAGCT | 13855 |
rs238836680 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571734 | CAGCTCTCCATACCC[A/G]CAATTAGAATTGTCT | 13855 |
rs238842866 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570366 | ATCCCCCGTAACTCC[A/G]TATTTTCAAGATCCA | 13855 |
rs238859590 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579621 | CGGCGACGCGGGAGA[A/G]GCGGGAGCGACCCGA | 13855 |
rs238946139 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537436 | ACTTCAAGACAAGGG[G/T]TACTAAAAGTAGGAT | 13855 |
rs239070591 | in-del | -/CTCTTTCAGGACTCAGGTTTGAACCCCAAAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539873 | TAAAAACACTGTCTG[lengthTooLong]CTCTTTCAGGACTCA | 13855 |
rs239105071 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540864 | ACACGTGCTGCGCCC[-/G]GCCCGCCGCCTTACC | 13855 |
rs239196082 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61578845 | GGTTTCTAGGGAGCT[C/T]AGACAATCTGCTCCC | 13855 |
rs239474948 | in-del | -/TGTATT | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581483 | TTGGGTTTCAGAAAA[-/TGTATT]TGTGATTTCTCTGTT | 13855 |
rs239484996 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563918 | CCCTATCAGGCCTGG[A/G]CACAAACCTGGAGCA | 13855 |
rs239650036 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61523528 | AAAGGCCTTCTGAAC[A/G]TTTCCCATCACACAA | 13855 |
rs239806325 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567430 | AATTCTTATTAATGT[C/T]TTGCCCTAATAGAAG | 13855 |
rs239864437 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560943 | CAGCAAGGGCAGAAA[C/G]ACTACTGTCTACTTA | 13855 |
rs239884434 | in-del | -/ACTG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540685 | ACAAGTTGACCTCTA[-/ACTG]ACTATGTGGCCAAGG | 13855 |
rs240007393 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61524081 | GAAAATATGAAACAA[A/G]TCATCCCTTCTGTAG | 13855 |
rs240142305 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539706 | GTGGCACATGCTGGT[A/G]ACCCCAGCTCTTGAG | 13855 |
rs240216010 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547412 | ACTGGGTGAGATGTC[A/G]TGATAAATGTATTTT | 13855 |
rs240284929 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571431 | TGCCTGCTCCCTGCC[C/T]GGGGCTCAGGTGGAA | 13855 |
rs240434157 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540966 | TCATCTGTTTGCATG[C/T]CTGCTGGGCAGCCAG | 13855 |
rs240434201 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61526933 | CTTTCACTCCAAGCC[G/T]GAAACTATACTTCCA | 13855 |
rs240439185 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61529377 | ACACCTGCTACCGGC[A/G]GGCGGAACTTAGGCT | 13855 |
rs240451373 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563230 | CCTGTTCCAAAAGAG[-/A]AAAAAAAAAAAACAA | 13855 |
rs240501055 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542752 | AGGGTGGGTAGAAAC[A/G]GATAGGTTGAAGGCA | 13855 |
rs240547731 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547993 | AAACACCTGAATAAA[C/T]GATATTACACTTACA | 13855 |
rs240570455 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61543050 | TCCATGAAGCTCTAG[A/G]AGAACCTGAGAACAG | 13855 |
rs240596936 | snp | C/T | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518503 | GAGTCAACTGACTGA[C/T]AATTCATCAAAAGAG | 13855 |
rs240605981 | in-del | -/TTG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525516 | CCTTAAACTGTTTTT[-/TTG]TTGTTGTTGTTGTTT | 13855 |
rs240610574 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61546092 | AGGTGCTCAGGTGTT[A/C]AGCCCCAGCACCTGC | 13855 |
rs240648923 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61520308 | TCTGCTCATCAAGGG[A/G]CACCATGACAAAGAG | 13855 |
rs240657358 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61555216 | AACTTACTCTGTAGA[A/G]CAGACTAGCCTCCAA | 13855 |
rs240672591 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61532817 | TCCTGAATAACTTGG[A/G]AATTGAGCTGCTCCA | 13855 |
rs240681989 | snp | A/G | | | downstream-variant-500B | Epn2 | Mm_Celera | 11:61517065 | TCAGAACTGATAGCC[A/G]TCTGGGCTAACATCT | 13855 |
rs240770790 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61533483 | GGGTTCAATGTGGAA[G/T]TTAGCATCCTGTTGT | 13855 |
rs240812787 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577565 | AATACCTGGGCTGGG[G/T]AGAATGCTAAGCAGT | 13855 |
rs240816315 | snp | C/G | | | intron-variant | Epn2 | Mm_Celera | 11:61522897 | TCAACTGTGGGCATA[C/G]ATAAGGGCCTGTGAT | 13855 |
rs240830416 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61549733 | CACAGCACTCAGGAG[A/G]CAGAGAATTAGAGGC | 13855 |
rs240878397 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575923 | GTACTAATTGCTCTT[A/C]CAGAGGTGCTGAGTT | 13855 |
rs240977429 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580985 | GAAGACAACTACAGT[A/G]TACTTAAATAGAATA | 13855 |
rs240994240 | in-del | -/CACACACGAACTCACT | | | intron-variant | Epn2 | Mm_Celera | 11:61523986 | ACACGCACTCACATA[-/CACACACGAACTCACT]CACACGGGGGCAGGG | 13855 |
rs241094410 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536863 | CTACCTACCTACCTT[C/T]TGGTTGATTTTATTC | 13855 |
rs241216484 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571133 | GCAAGTATTGGACTT[A/G]GAAAGATAGCTCAAT | 13855 |
rs241550254 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548249 | GACCCTCCCTACAGA[-/T]TCCTCAGGCAGCCCA | 13855 |
rs241592907 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558050 | TTAGGATTTCTTTTT[G/T]TGTAAAAGAGTTTGC | 13855 |
rs241610791 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61524954 | ACTGACCTCGAACTT[C/T]TTTTTGTTATAGTTT | 13855 |
rs241680453 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538203 | TAGAGGCCAGTCTGG[A/G]CTACCAGAAGACCTG | 13855 |
rs241808970 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576931 | AAATGCCCAGAGTAC[C/T]CTAACAGACCTTGTG | 13855 |
rs241893299 | snp | C/G | | | intron-variant | Epn2 | Mm_Celera | 11:61522744 | AACGTAGTAAGGGCT[C/G]GCAGTGTAGGAAATA | 13855 |
rs242105176 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547896 | TAAGGTCCACATCTC[A/C]CATCTCCAGCATGTA | 13855 |
rs242134749 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61520076 | GTGCCTAAGAAAGGC[C/T]ATGCAGTGTCCCAGG | 13855 |
rs242156748 | in-del | -/GG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538304 | GTGGGGACAGCAGCA[-/GG]GGGGGGGAAGTTAAG | 13855 |
rs242165011 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61551234 | CCAATCAATAAATTA[C/T]TTGATTGACTGGGTA | 13855 |
rs242167316 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61565302 | GTCTGACCCAGGCCT[A/C]TGAGAGCTTGCTAAC | 13855 |
rs242167576 | in-del | -/AAA | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581015 | AAATCAATAAATCTT[-/AAA]AAAAAAAAAAAAAGA | 13855 |
rs242257660 | in-del | -/GCGCGC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61533427 | TGTGTGTGTGTGTGT[-/GCGCGC]GTGTGTGTGTGTTCG | 13855 |
rs242275261 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563748 | ACAGTCCATTCAAGC[C/T]TAAGCTTTCCTTCTG | 13855 |
rs242296717 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553234 | CTGGATGATGCTACT[C/G]CTTAGCTGTTGGCAT | 13855 |
rs242298980 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536094 | TACCCATGGAAGGAG[C/T]CATTGTGTCTAATGG | 13855 |
rs242363187 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61552291 | GCCACGCAGCCTCCT[G/T]TGATTCTTATGTCCA | 13855 |
rs242559645 | snp | C/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580734 | CAGCTCCTCAAGCAG[C/T]GTGCCTGCCTGGACT | 13855 |
rs242623646 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577793 | GGCACCATACACCCC[A/G]CAGCGAAAGGAGACC | 13855 |
rs242671172 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61541217 | GGTCTTTCTTCTATT[A/G]CCTAGTTATTCCTGT | 13855 |
rs242674302 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558231 | ACCTCTTTAGCTGTG[A/G]TTTTCTTTACTCAGT | 13855 |
rs242732842 | snp | G/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61557176 | TTCCTTGCTTTATTA[G/T]AACAACTATACCTCA | 13855 |
rs242745765 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61528698 | TACCCACCACCAGTC[G/T]GGATACCTGCAACAC | 13855 |
rs242793348 | in-del | -/AGGCC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558887 | GATCTCGTAAGTTCG[-/AGGCC]AGCCTGGTCTACATT | 13855 |
rs242863952 | snp | A/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61557494 | GGCCCAAGTGCTTTC[A/T]GCACTGTATTTTAAA | 13855 |
rs242936131 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572635 | ATCTCCAGACCCACA[C/T]AAAAAGCTCAGCACA | 13855 |
rs242954098 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542639 | CACAGCGACAGTATC[G/T]AGAAATTCCTATCAG | 13855 |
rs243024632 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61555827 | TCTCTTTAGGAAGGG[C/T]CTTCCCACCAGGCAG | 13855 |
rs243210690 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61529059 | CCCCTAACTCCACAG[G/T]AAAGCAGCAGACACG | 13855 |
rs243365163 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539987 | GACACCGGGCACAAA[C/T]GTGGTTCAGGTATAT | 13855 |
rs243371974 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61565354 | ACACCAGCTCTCCTG[-/A]AAAAAAAAAAAAGCA | 13855 |
rs243442803 | in-del | -/TT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558326 | GATATGGGAAAGTGG[-/TT]TTTTTTTTTTATTAA | 13855 |
rs243483618 | snp | G/T | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518345 | TAAATGGAAGTCCCT[G/T]GCAATCCCTGCATTC | 13855 |
rs243581072 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61523883 | AGGAAAGGGGCTTGC[A/G]ATCAAGCCACTCAGG | 13855 |
rs243638256 | in-del | -/TA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525173 | CCACAATATACTCTT[-/TA]AAAAAAAATCCTGGC | 13855 |
rs243680319 | in-del | -/ACCCACATGATG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539904 | GGTTTGAACCCCAAA[-/ACCCACATGATG]ACTCACAACCATCTA | 13855 |
rs243752825 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530822 | AATGTGTGGGGTTTA[-/T]TGTTTTGTTTTGTTA | 13855 |
rs243795840 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61549934 | GCAAAGCTGAGCACA[A/G]CAGCTGCTCTGGAGA | 13855 |
rs243873824 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562917 | CTGCAAATCTCCATG[C/T]ATACCAACAGAAGGG | 13855 |
rs243996283 | in-del | -/AA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61578200 | CACAAATGCCCTAAG[-/AA]AAAAGCTGCAGTTCC | 13855 |
rs244011090 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525197 | TCCTGGCTTACATTT[C/T]TTTCCAATAAATCAA | 13855 |
rs244053572 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570992 | TTTAATCCCTCCCTG[C/T]ACTTGAGAGGCTGAA | 13855 |
rs244053592 | snp | A/C | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556154 | GGCCTCTTGTCATCT[A/C]AAACAGCAGAGAAGC | 13855 |
rs244158168 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570129 | AAGATGTTGCTTTCC[A/G]CACAGCAGGGCCATT | 13855 |
rs244189541 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567259 | ACCAAGATGGCACAT[-/G]GACAGAAGACACTGG | 13855 |
rs244239926 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581685 | CCACCATACAGAGAC[A/G]TGATTAGACAGAACA | 13855 |
rs244285194 | in-del | -/CATCCATCC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547017 | CCATGGATACAAAAA[-/CATCCATCC]CATCCATCCTGCTTT | 13855 |
rs244320112 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61532237 | TATTATTTTAAGTAA[C/T]AAGAATAGCAGCAAA | 13855 |
rs244325045 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560800 | TCATCTCTCAGGAGG[A/G]TTAAGTAATATTGTC | 13855 |
rs244365972 | snp | A/G | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518031 | AATACTTTTCTTAAC[A/G]GTGAGTAGTGAGGAC | 13855 |
rs244379626 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531574 | AAGTACGCTAAAGAG[C/T]AGCTGAGGCTGACAC | 13855 |
rs244421668 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61578188 | CACAATCATTAATCA[C/T]AAATGCCCTAAGAAA | 13855 |
rs244429868 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574220 | GGCAAATTTCTGAAT[A/T]CAAGGCCAGCCTGGT | 13855 |
rs244439392 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539520 | TCTCCCAGCACCTCA[C/T]ACACCACTGTGACAG | 13855 |
rs244476348 | in-del | -/A | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518367 | CTGCATTCCAGGTAC[-/A]AAAAAGGGATTAGTT | 13855 |
rs244480016 | in-del | -/CCAAGGC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559646 | ACCATGTCATAAGGT[-/CCAAGGC]CCAGAACAGCAAATA | 13855 |
rs244492808 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572592 | CTCAGTGGATAAGAA[A/T]ACATGCTCTACTAAC | 13855 |
rs244526966 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536917 | AATACTTAGGTCTCT[A/T]CTTTCTCATGCTCAA | 13855 |
rs244527597 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576260 | CAGAAAATACATTTG[A/G]GGGTTTGAGATTTGG | 13855 |
rs244622840 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61561885 | TCTGCAACTCCTAAC[A/G]CAAAACCAACCTATG | 13855 |
rs244640886 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553631 | CAAGCCTAAATGACC[C/G]AAAGCATCCAAAACA | 13855 |
rs244674050 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567003 | AGAAACAAACCACTT[A/C]CTGCCCTCACATATG | 13855 |
rs244715289 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563612 | TGCCATGAGCAGGGT[A/G]GAGCTAGGCACCAAC | 13855 |
rs244716119 | in-del | -/TAATG | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581709 | AGAACAGGGTAGCTC[-/TAATG]TAAGAGAGGAGACCA | 13855 |
rs244767330 | snp | A/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581273 | TCGGCCCACGATATA[A/T]TAAAGCTGGAGGCCA | 13855 |
rs244945037 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531000 | CGACCCTGGTCCGAC[C/T]CACTAGGAATTCTCT | 13855 |
rs244984675 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568347 | AAGTGCTCCAAAAAC[A/T]ATGTAAGCAGATGGG | 13855 |
rs245016993 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61545835 | ACTAGGTATTTGAGT[C/T]CCTGTAGGTTTGGAA | 13855 |
rs245084507 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576132 | CTGATGGTTGTGAGC[C/T]ACCATGTGGTTGCTG | 13855 |
rs245120461 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61545298 | TGTTCTGAAGGATAT[A/G]GGCTTGGAAGCCCGT | 13855 |
rs245198935 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559727 | CAGACTCAGCTAGCC[A/G]TGACAAGCCTGAAAA | 13855 |
rs245433198 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538751 | GGTTTTTTGTTTTTG[-/T]TTTTTTTTTGAGACA | 13855 |
rs245590034 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61578137 | AAACATTCAAAAAAA[-/G]AAAAAAAAAACCAAG | 13855 |
rs245612073 | in-del | -/AG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548059 | GTAAGATAAAGAAAC[-/AG]AAATCTCAAGACAAC | 13855 |
rs245703933 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579145 | GGAGTGGGGGCCGGG[A/G]AGGGGAATCCAGTCC | 13855 |
rs246071019 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61523241 | GGCTAGAGAGTATTA[A/G]AGAGTTTCTACTGCT | 13855 |
rs246077011 | snp | G/T | | | intron-variant | Epn2 | Mm_Celera | 11:61524025 | GGCAGGGGCGGGACT[G/T]TAAATGTTAACCCCG | 13855 |
rs246084979 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525019 | TGTGTAGCTCTGGCT[A/G]TCCTGGAACTCACTC | 13855 |
rs246108709 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61541057 | GCAGCTACAGGATGT[C/G]GTTCCACAGTGGTCC | 13855 |
rs246137825 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538472 | TTGTCCACAGTGTGT[A/G]TCAATGTGTCCATAA | 13855 |
rs246139731 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61524171 | CCTGAGCCATTCCTT[C/T]AGTTTATCACACCTT | 13855 |
rs246151001 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537283 | GGCTCTGAGCAGACA[C/T]GCTGCAGCAATGAGG | 13855 |
rs246183028 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540448 | TGGTGCCCTGGTCTG[C/T]TTACAAATAATCCCT | 13855 |
rs246205208 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567968 | TTCACTAAATTATGT[C/G]TTTTCATTCATTGAC | 13855 |
rs246456007 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527404 | ATCATATCCAGCCCC[A/T]GCTGCCCTTTTTTAA | 13855 |
rs246481084 | in-del | -/GATCTCT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61549737 | CACTCAGGAGGCAGA[-/GATCTCT]GAATTAGAGGCCATC | 13855 |
rs246502925 | in-del | -/A | | | intron-variant | Epn2 | Mm_Celera | 11:61520579 | TCTGGCACTGGGCAC[-/A]AGAGTCTCTTGGGCA | 13855 |
rs246506177 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61543144 | AAACAGTTCTAACCC[C/T]GACATCAGTAACTGT | 13855 |
rs246520243 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572422 | CAAGCCCCCTCCCAA[C/T]CTGAGAGCACTAACC | 13855 |
rs246597315 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61545243 | TCACTTTCAGAAAGT[-/A]AAAAAACAAAAAGGT | 13855 |
rs246624392 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548117 | TCGGCAGCCCTGCTA[C/G]AGTTGCTCAGTCCCT | 13855 |
rs246638269 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554756 | CATTTTGCAGGAGAC[A/G]ACACAGAAACTTCTC | 13855 |
rs246679229 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574014 | TACACACTTGCCTTT[-/A]AGAAAATAATAATAG | 13855 |
rs246714991 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539432 | CAGGAAAGGGGGCGG[A/T]GAGGAAGAATGCTGA | 13855 |
rs246914768 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579980 | CCCTTAAATCCTCAA[A/G]CACAGAACCCCGCCT | 13855 |
rs247078967 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574281 | CCTGTCTTAAACCCC[C/T]CCCCCCAAAAAAAAG | 13855 |
rs247126148 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61561059 | TGAGAACTACGGGGG[A/G]AAATGGCTAACAGCA | 13855 |
rs247248004 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554630 | CAAAAAGCAACAGCA[G/T]CTGCAGCTGAACGGA | 13855 |
rs247261483 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581217 | TCACAAGAAAGAAAA[A/G]GCACCTGGGTCTCAA | 13855 |
rs247281218 | in-del | -/CTCCACCATACTA | | | intron-variant | Epn2 | Mm_Celera | 11:61522711 | AGTGCCTCCCACTGC[-/CTCCACCATACTA]CTCCAAACGTAGTAA | 13855 |
rs247301301 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61521317 | AGAAACTTGTGCCAG[A/G]CATTATAACAGGGGC | 13855 |
rs247499380 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579190 | ACGTGGGGAAGAGTA[C/T]CCCCTTCCCCCGGTC | 13855 |
rs247681905 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558879 | GGCAGAAGGGATCTC[A/G]TAAGTTCGAGCCTGG | 13855 |
rs247685442 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542415 | CCTCCAATAAGCCTT[A/C]TTGGGTCTTCTCTAG | 13855 |
rs247785910 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558428 | AATTTTGTGCAAGCA[C/T]CACCATCAAATTAGA | 13855 |
rs247837527 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61561053 | AGGGCCTGAGAACTA[C/T]GGGGGGAAATGGCTA | 13855 |
rs247864645 | in-del | -/CT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566610 | GCAGGCCATTCCATC[-/CT]CCCCCCACTAAGTAC | 13855 |
rs248019018 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569622 | AGGCAGCACCCAAAA[G/T]AGACGCCATATATAC | 13855 |
rs248056643 | in-del | -/CATG | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556488 | TGACTGGTATGAAAC[-/CATG]CATGCATGCATGTGG | 13855 |
rs248064028 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548616 | AAACCTGTCAGAAAA[C/T]AGATAAAACCTTTTT | 13855 |
rs248135987 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61549641 | TTCCAGAACCTATGC[A/G]ACAATTCAGGGAACC | 13855 |
rs248173314 | in-del | -/T | | | intron-variant, utr-variant-5-prime | Epn2 | GRCm38.p3 | 11:61555481 | ACATATAAATAAATC[-/T]TTTGGGACACAGCGA | 13855 |
rs248183301 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562263 | TCCAGCACTTGGGAA[A/G]CAGAGATAAGCAGAT | 13855 |
rs248186049 | in-del | -/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571502 | TTTCTTTACCCTCTG[-/C]TAAAGTACTCACTTC | 13855 |
rs248297265 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61561510 | CTCCTCTCCTCCTTG[C/T]ACCTTGTGGAGGGAA | 13855 |
rs248378032 | snp | C/T | | | downstream-variant-500B | Epn2 | Mm_Celera | 11:61516945 | ATAAATAAACCCTAG[C/T]CTTCCCAAGTTGCTT | 13855 |
rs248382979 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550522 | CAAGGGAACTCAGTG[A/C]TCCCCAAGAAAGTAG | 13855 |
rs248441075 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554996 | GCTGCAGGTGTCTAC[C/T]CTTTAATCTTCATAA | 13855 |
rs248543950 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61528082 | AATGCATGCAAATCT[A/G]AGCTCCTAACACACA | 13855 |
rs248638991 | in-del | -/ACACTGTAGTTGA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531196 | ATTATGTATATGGGT[-/ACACTGTAGTTGA]ACAGCTGGTTTTAAG | 13855 |
rs248775066 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540246 | GTCACTGCTTTCTAT[C/G]AGATAGATCAGGTTC | 13855 |
rs248786501 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61555910 | AAATGATCAAGAATG[C/T]GTTTTTTCAAGCTGC | 13855 |
rs248788721 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538886 | TAAAGGTGTGCACCA[C/G]CACGACCGGCTGTTG | 13855 |
rs249040274 | in-del | -/AAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568730 | AAACAGTCACAACAC[-/AAA]AAAAAAAAATACCAT | 13855 |
rs249044283 | in-del | -/TGTTGTTGC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550070 | TGGTTTTGTTGTTGT[-/TGTTGTTGC]TGCTGCTGCTGTTGT | 13855 |
rs249103407 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61551092 | CACTAGTTTACACCA[-/G]GCTCCATGGTTACTA | 13855 |
rs249149851 | snp | A/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61578601 | ATCCTTAAGTGTCCC[A/T]GAGTTGGGGCTTCCA | 13855 |
rs249190432 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61523347 | GGATTTGACATTCTC[A/G]GGCCTTCTCAGGCAT | 13855 |
rs249197096 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61555129 | GATTTCTAGTCTCTT[G/T]TTTTGTTTGTTTTTT | 13855 |
rs249235176 | snp | C/T | | | downstream-variant-500B | Epn2 | Mm_Celera | 11:61516929 | ACAGTGATGTGGAAG[C/T]ATAAATAAACCCTAG | 13855 |
rs249252749 | in-del | -/AAAAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564842 | CCAGACTTCTGCTTT[-/AAAAA]AAAAAAAAAAAAAGC | 13855 |
rs249259335 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536320 | CAAAAAGAAGGACAA[A/G]TTAATTTCATAGCTT | 13855 |
rs249275001 | in-del | -/TGTGTGTGTG | | | intron-variant | Epn2 | Mm_Celera | 11:61524264 | GTGTGTGTGTATGTA[-/TGTGTGTGTG]TGTGTGTGTGTGTTC | 13855 |
rs249328424 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581417 | TGAATGAAATCACAT[A/G]TTATGTACCTGCTTT | 13855 |
rs249332255 | snp | G/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61555738 | ATGGGGAGCAACTGT[G/T]TCTTGCCCACCCATG | 13855 |
rs249345133 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569063 | ACAGAACTGGCACCC[A/C]CAAGCCCCATCTAGA | 13855 |
rs249597095 | snp | C/G | | | intron-variant | Epn2 | Mm_Celera | 11:61524416 | TGTTCTGTGCACACA[C/G]TGACAACTGTTGGGC | 13855 |
rs249624167 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61523844 | TCTCACAAGGATGGC[A/G]CAGGGTTGGTGGGAC | 13855 |
rs249672900 | in-del | -/TG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559927 | CTCAAGAATAATTAC[-/TG]TGGGGCTGGAGAGAT | 13855 |
rs249697047 | in-del | -/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527674 | GCACAGCAGTTCCCA[-/C]CCTGCAGTAGTCCTA | 13855 |
rs249742880 | in-del | -/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548509 | AGATAGGCTGAGGAG[-/C]CCTGTCTGTGCCTGA | 13855 |
rs249749628 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574321 | CTAGTAATAAGTGTA[-/T]TTTTTTAGAAACTTG | 13855 |
rs249796773 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581669 | TTTGATGAAGAATGA[A/G]CCACCATACAGAGAC | 13855 |
rs249853835 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566252 | AGCTTTGTCTACAAA[A/G]CAGTTCCAAAATAGT | 13855 |
rs249870720 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560407 | CCCACAGCAAATCTG[A/T]CAGCCCCAATAATGG | 13855 |
rs249889692 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61529917 | TTTTCAATAGCACCT[A/C]CACAGGACACATAGC | 13855 |
rs249922769 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564591 | AGCCAGGTAGACCTA[A/G]CACCGCTGCATGGTA | 13855 |
rs250058937 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61555436 | TCTGATGCCCCTTTC[C/T]CGTGTGTCTAAAGAC | 13855 |
rs250090983 | snp | A/G | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61519076 | CTTGTCCACACCCTG[A/G]AGATAACTGGGGGTG | 13855 |
rs250195616 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61532809 | GGGCTAACTCCTGAA[G/T]AACTTGGAAATTGAG | 13855 |
rs250207026 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61526676 | AGGCTACTGGCTAGT[A/G]TAGTGTAGGATGGAG | 13855 |
rs250220282 | in-del | -/AA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577331 | TTTAACTTCTAGAAG[-/AA]AAAAAAAAAAAACAC | 13855 |
rs250260971 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61548295 | AGTGAACCTTCCTCT[C/T]CCTGGATTGCTGTGG | 13855 |
rs250361108 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61578072 | GATCTCTGTGCATTC[A/C]AGGCCAGACTGACTA | 13855 |
rs250499251 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61574571 | CAGAGTGTTGTCAGG[C/T]TTTATCTACTGAATT | 13855 |
rs250600098 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559261 | CTGTGTAACTCTGGC[C/T]GTCCTGGAACTCTGT | 13855 |
rs250640873 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566278 | ATAGTCAAGGCCATT[C/T]GGAGAAACCCTGTCT | 13855 |
rs250660388 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558152 | AAATACAGTTTTGAC[C/T]TGTCATGTGGATACT | 13855 |
rs250672803 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537452 | TACTAAAAGTAGGAT[A/C]ACCCCTACACACTGT | 13855 |
rs250688549 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554132 | CTAACCTGCAGGCCT[C/T]ACATACTCCCTCCCC | 13855 |
rs250942247 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61555688 | AACTGCAGGCCTAGG[-/A]AAAACCCTCTTGTCT | 13855 |
rs250991261 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61566026 | CTTGACACTTAAAAT[A/G]ATTACAGAGGTCAGC | 13855 |
rs251041348 | in-del | -/GCTTCCA | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61578610 | TGTCCCAGAGTTGGG[-/GCTTCCA]GCTGTGTCAAACACC | 13855 |
rs251051721 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61564273 | CTATTTCCGTGGGCC[C/T]CAGAGGGCAGAAGTC | 13855 |
rs251258168 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540977 | CATGTCTGCTGGGCA[A/G]CCAGGTTAAAGACAG | 13855 |
rs251275919 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570756 | AGTTAAGAACTCTTT[A/G]GTAGCCGGGCGTGGT | 13855 |
rs251365792 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542880 | AGTGAAGAGAAAAGG[-/A]AAAAAAAAATTGGCT | 13855 |
rs251497238 | in-del | -/CACGTAT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531547 | GAAGTTGGCAAGCTC[-/CACGTAT]CACTGTAGCCAAAGT | 13855 |
rs251502518 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530243 | CAAGCTCTGAGCTGG[C/T]GGGGAGAGGTGGGGA | 13855 |
rs251541372 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61529098 | CCGCCGCCCTTAGGA[A/G]AGAGAAAGGGCAATG | 13855 |
rs251557243 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61528840 | AAATGACATAGATCA[C/T]CAGGGATAAACAGTT | 13855 |
rs251621477 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61549779 | AGTAACTTCCTCCAG[A/G]ACAGGCCCTGTCTCA | 13855 |
rs251675239 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550909 | AGGACAAAGGACTGG[A/C]GTTCAGATCCCAGCA | 13855 |
rs251705191 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61573430 | TCAGCGCGGGATTTA[A/G]AAGCATTCTCATTTC | 13855 |
rs251712119 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562224 | ACTCAGTATTAGGCA[C/T]GCATAGTGATGCATG | 13855 |
rs251823451 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536426 | GACTGCTTACCACAA[C/T]GCTTTCTCCAGCTCT | 13855 |
rs251912510 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61535474 | AAGATAGTACTCAGT[G/T]TTCATCTCAAACCCA | 13855 |
rs251922182 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61551333 | TTTCTAAAAGAAGCT[A/G]ACAGCCTGTGAAGTG | 13855 |
rs251934179 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61557301 | GTGAGTCTAACACCA[C/T]ATAGCAGTGAGTGTA | 13855 |
rs251968797 | snp | C/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580763 | CTGTGCCCTGCTTCC[C/T]GCCATGTTGGTAATG | 13855 |
rs252042922 | in-del | -/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61541973 | TGTAGCTTTGCTAGT[-/C]CCACAGTACTTGGTG | 13855 |
rs252141676 | snp | A/C | | | intron-variant | Epn2 | Mm_Celera | 11:61520638 | CCAGCCACAGGGCAA[A/C]CTTTCTCTAGGGATA | 13855 |
rs252178549 | snp | A/G | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518504 | AGTCAACTGACTGAT[A/G]ATTCATCAAAAGAGT | 13855 |
rs252212180 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61533033 | CCTGGCTAGCAGCAC[C/T]CAGTACCCAACCTAA | 13855 |
rs252272270 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579039 | TCGCCCACCCGGACT[C/T]GCCCAACAGGGCCGC | 13855 |
rs252322685 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581604 | GAAGCCTTCAGCAGT[A/G]AAGACTCAAAAGACC | 13855 |
rs252330993 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577597 | AAGAGCACATACTTT[C/T]TAAAGAACCAGAGCT | 13855 |
rs252583456 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539190 | CTTTCAGAGAGAACA[C/T]CAACAAAGCCCACAG | 13855 |
rs252584368 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61524603 | GCCTATTTTGCAACC[A/G]TTTTATGTTTACTTG | 13855 |
rs252595097 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537937 | CCAGCATAGCTCCAC[A/G]TACAATGAGACACCT | 13855 |
rs252604069 | snp | C/T | | | synonymous-codon | Epn2 | GRCm38.p3 | 11:61546649 | GCTGGATGGGCCCCA[C/T]GGGTCATTGGAGGTG | 13855 |
rs252641558 | in-del | -/AC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536798 | GTACTTTAAAAATAT[-/AC]ACACACACGCGCGCG | 13855 |
rs252688626 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560543 | AACTTCTTCTTCCTA[C/T]AACGCCACAACTGAA | 13855 |
rs252803865 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537152 | ACTGAATGAAAATCC[A/G]GGAAGAAACGTCACA | 13855 |
rs252837024 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558488 | CTCAAATCCCCCATA[-/T]TCAATTAGTAGTCAT | 13855 |
rs252999982 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61571144 | ACTTGGAAAGATAGC[C/T]CAATGGTTAAGGAAA | 13855 |
rs253070322 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570448 | AATGTCTAACACCAC[G/T]TTTTACATTGTCTAT | 13855 |
rs253192077 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61565358 | CAGCTCTCCTGAAAA[A/G]AAAAAAAAGCAACAC | 13855 |
rs253216349 | snp | C/T | | | intron-variant, utr-variant-5-prime | Epn2 | GRCm38.p3 | 11:61555534 | AGGTCTTGAGTTCTA[C/T]TCTCAGCAACCACGA | 13855 |
rs253328483 | in-del | -/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537524 | AATTCACAGCCACCA[-/C]CCACACAATCAGCTG | 13855 |
rs253391153 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568558 | GCACTGAGATACTGA[C/T]CACAGACTTGTGTAA | 13855 |
rs253507052 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540899 | CCCCCCTCACTCCCG[A/C]TGTGGAGAAAACCCA | 13855 |
rs253534433 | in-del | -/TA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559086 | TCTATGTTGTATGGC[-/TA]TGTTTTCTCCTTCTG | 13855 |
rs253559987 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539611 | TAAAAATTCCTGGGC[C/T]GGGGCTCAATATGGC | 13855 |
rs253560000 | snp | G/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556453 | GAGGTACCCCAGGTT[G/T]TTTATCTACTGTTCA | 13855 |
rs253571602 | in-del | -/TTGTTT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530821 | AATGTGTGGGGTTTA[-/TTGTTT]TTGTTTTGTTTTGTT | 13855 |
rs253572743 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61546013 | GACCAAAAGCCCCTT[A/T]GTAAGTAACTCAATC | 13855 |
rs253625081 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61528592 | ATAGATAAAGTTTCT[C/G]AGGCAGAATAAGACA | 13855 |
rs253637090 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560137 | AAATCTTTTTTTAAA[A/G]GGGGGGGGGGATGGA | 13855 |
rs253658451 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531367 | TGGGTGGTTGTGAGC[C/T]ACCATGTGGTTGCTG | 13855 |
rs253734090 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558825 | CATATAGCTGGGCAT[A/G]GTGGTACACACCTGT | 13855 |
rs253758364 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61541763 | GGTGGGCTGTGCACC[A/G]TAGCAGGCAGGACAA | 13855 |
rs253810609 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61567926 | GGAGTAACCTAGATT[-/G]TAAAATGTTGAAGCT | 13855 |
rs253919690 | snp | C/T | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61517780 | GCATGTAGACTCAGA[C/T]CCAGGAGGGGCTTAA | 13855 |
rs254077826 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562118 | TGAAAGACCCATACA[C/T]AGCCACACAGAACTT | 13855 |
rs254138727 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576185 | GAAGAGCAGTCAGTG[C/T]TCTTAACTGCTGAGC | 13855 |
rs254203157 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61522315 | ACACAAACATGCATG[C/T]ACACACACAAAGTTG | 13855 |
rs254297768 | in-del | -/GGGAGTTCTCTTT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61551844 | GGGGACAAGTGAAAA[-/GGGAGTTCTCTTT]CCTCTTACAACATAA | 13855 |
rs254442689 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61533393 | AGTGTCTTCCTCCTG[lengthTooLong]GTGTGTGTGTGTGTG | 13855 |
rs254459445 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531688 | ACCTGCTGCCCATGT[A/C]ACAATGCATGGGTCT | 13855 |
rs254589418 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547322 | GCCGGGATTAAAGGC[G/T]TGCACCACCACACCC | 13855 |
rs254654056 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61544920 | AAATTACGATAGCCA[A/G]AAATACAAGAAAATG | 13855 |
rs254660150 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531674 | CCCCTCACCCTTCTA[C/G]CTGCTGCCCATGTCA | 13855 |
rs254679554 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547080 | CTAAACAATAAACTC[A/G]TTTAAACCTTAAGCA | 13855 |
rs254684084 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525657 | TCAAAGGTATGCACC[A/G]CCCTCCCAGCTGTAA | 13855 |
rs255015561 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554364 | CAATATGGCCCCTCT[A/G]AACTGCTGCACTACC | 13855 |
rs255050098 | snp | A/C | | | intron-variant | Epn2 | Mm_Celera | 11:61521637 | ATAGCACAGCAACTG[A/C]TAAAACGAAGCACAT | 13855 |
rs255060635 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572132 | ACAAAAATCAAAATC[A/T]CAGTTTAACACACCG | 13855 |
rs255081130 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553110 | TAGGGGCAGGCTGTA[A/G]ATGACAGTCCCAGAA | 13855 |
rs255132710 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538826 | CGACCAGACTGGCCT[C/G]GAACTCAGAAATCCG | 13855 |
rs255196898 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575442 | TCTTGCAGCTTAACC[C/T]AGCAAATCTAAGAGT | 13855 |
rs255234151 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579619 | GCCGGCGACGCGGGA[A/G]AAGCGGGAGCGACCC | 13855 |
rs255382446 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579634 | GAAGCGGGAGCGACC[A/C]GAGCCTGTGCAGCGT | 13855 |
rs255395482 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542186 | CAACAGAGAGACACA[-/G]GGGCCCAGTCTTTCT | 13855 |
rs255405524 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61522833 | TCAGTCTGCCACCCA[A/G]AAAGGAGACCAGAAC | 13855 |
rs255495421 | in-del | -/AGA | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581824 | TACAGGCTAACTTAC[-/AGA]AGAACTTCTCCATGG | 13855 |
rs255631245 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61565127 | AGAGCACGCAGCAAT[G/T]CCAAAAGTTTGGTTC | 13855 |
rs255635805 | snp | C/T | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61580975 | TGGTGTGTCTGAAGA[C/T]AACTACAGTATACTT | 13855 |
rs255702051 | snp | A/C | | | intron-variant | Epn2 | Mm_Celera | 11:61521201 | GAGTAGAAATGAGGT[A/C]AGAGATCAGAGGTCA | 13855 |
rs255801212 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538305 | GTGGGGACAGCAGCA[-/G]GGGGGGAAGTTAAGG | 13855 |
rs255970157 | snp | A/C | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61517700 | CCCAAACCTTTCCCT[A/C]GGCCTCTGGTCCTGG | 13855 |
rs256042531 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527501 | ACTGCCCTGACAACC[A/G]GGGAGAATCCTTGTG | 13855 |
rs256056926 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61540840 | TCACCTGCTTTCACG[A/C]ATGCACACACACGTG | 13855 |
rs256070468 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61570814 | GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCG | 13855 |
rs256093294 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562187 | GACTCCACAGACACA[C/T]ATATACATACACAAT | 13855 |
rs256114019 | in-del | -/AAG | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575810 | GAGACCCTGCTTCAA[-/AAG]AAGAAAAGAAGAAAG | 13855 |
rs256244791 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61552262 | CTGCAACAAGCTCAG[A/G]TGAGCTGACAGGTGC | 13855 |
rs256305980 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61550360 | TACTCCACAGCAAGT[C/T]ATGTTGTTATAGGCA | 13855 |
rs256322074 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61544613 | TGTAAGAAGGGTCTG[A/G]TGAAACAACCAGGCT | 13855 |
rs256410038 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563121 | AGAGGGTAAGAGCTG[A/G]GCTTAGAGGCATATA | 13855 |
rs256464982 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568365 | GTAAGCAGATGGGCC[C/T]GCCAGCCTGGGAACT | 13855 |
rs256500328 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577733 | CCCAGACACACACAC[-/T]TTTTTTTTTTTAAAG | 13855 |
rs256617669 | snp | G/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61557040 | TAAAGGAGGATGGGG[G/T]TTGGGAGGGGCTGCA | 13855 |
rs256630495 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577980 | CTAGGAAAACCAAAC[-/T]TTTAAAGTCACAAAA | 13855 |
rs256676427 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530589 | CTTCTGGCCAGGAAA[A/G]GACTAAACACCTACT | 13855 |
rs256682007 | snp | C/G | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61555858 | ATCAGGTCTGAGTAT[C/G]AAACAGTGTGGTCTC | 13855 |
rs256734136 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61535698 | AAGAGTTCCTGAAGA[A/G]CCTTCAGCCACGTGA | 13855 |
rs256738830 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536200 | TTTAGCCTCCTGCAC[C/T]GGGACCCACAGAGTA | 13855 |
rs256781985 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558605 | ATAGCCCTTTTTTTT[G/T]TTTTGTTTTGTTTTG | 13855 |
rs256783887 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569391 | AACAGAAACACAAGG[A/T]TTCTTTAGAGATGGG | 13855 |
rs256949136 | in-del | -/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61545181 | GCACCCTGAAGGTTG[-/C]ATTAGGAAGATAGCA | 13855 |
rs256962382 | snp | A/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61556029 | TATTTGTTTTCCTAA[A/T]CTTATATTCTTAGGA | 13855 |
rs256978711 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569845 | AGAAAACACACTGCT[C/T]TAAGTGTGGGCATTC | 13855 |
rs257047159 | in-del | -/TGTGTGTGTGTG | | | intron-variant | Epn2 | Mm_Celera | 11:61524263 | GTGTGTGTGTATGTA[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 13855 |
rs257080190 | in-del | -/TT | | | utr-variant-3-prime | Epn2 | Mm_Celera | 11:61518619 | TGTAATCAAATTCCG[-/TT]TTTTTTTTTCCTATA | 13855 |
rs257276400 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61526960 | TCCAGATCCTCTCCT[A/T]TGTGTGGGATGCTTT | 13855 |
rs257400628 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525049 | CTGTAAACCAGGCTG[A/G]CCTTGAACTCACAGA | 13855 |
rs257400692 | snp | A/C | | | intron-variant | Epn2 | GRCm38.p3 | 11:61539750 | AGAATCAGAAGTTCA[A/C]GGTCATCCTTGGCTA | 13855 |
rs257470975 | snp | A/C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538634 | CAAATCCCCTCAGGG[A/C/T]CCAAACTGGGACCTA | 13855 |
rs257491294 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61554642 | GCAGCTGCAGCTGAA[C/T]GGAACTGGTAAATGA | 13855 |
rs257496370 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61555614 | AATCTCTAAAAAAGG[-/A]AAAAAAGATAAATCC | 13855 |
rs257533254 | in-del | -/AAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577330 | TTTAACTTCTAGAAG[-/AAA]AAAAAAAAAAAAAAC | 13855 |
rs257534507 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568258 | GTAAAGAAGCCTGTT[-/A]AAAATTCCAGCTATC | 13855 |
rs257649643 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527767 | CAGGTGGGGCTGGAG[C/T]GCCTTCCTACTCTCT | 13855 |
rs257671491 | in-del | -/AGACAGAC | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575853 | GAAGGAAGGAAGGAA[-/AGACAGAC]AGACAGACAGACAGA | 13855 |
rs257709607 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61547457 | GGGTACTGAACTCTG[A/G]GCCACATGCATATCA | 13855 |
rs257711307 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61532102 | AGCAATTAAGAAATT[C/T]CATGTGCCAGGAAAA | 13855 |
rs257733576 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559055 | CTCTGCTTTATGAAT[A/G]ATGATGTTAGGAACA | 13855 |
rs257779678 | snp | A/G | | | intron-variant | Epn2 | Mm_Celera | 11:61524857 | ATCTTCACACATACT[A/G]TGATAATGATCCTTT | 13855 |
rs257820472 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560956 | AAGACTACTGTCTAC[C/T]TACCCCTAGCCACCA | 13855 |
rs257830932 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61531428 | GTCAGTGCTCTTAGC[C/T]GCTGAGCCATCTCGC | 13855 |
rs257885529 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61524123 | TGTTTAAACACTGCT[C/T]CATTTCCAGATCCAC | 13855 |
rs257936192 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61578853 | GGGAGCTCAGACAAT[C/T]TGCTCCCCCTGCAAA | 13855 |
rs258005677 | in-del | -/TTA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61576452 | AAATCTTTTTTTTTT[-/TTA]AATTAAGAAAGCTAG | 13855 |
rs258056746 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553988 | AGATAATTCAAGACA[G/T]GGTTTTTCTGTGTAG | 13855 |
rs258089497 | in-del | -/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61526190 | GGCCAGACTCCCTAT[-/G]CTCCTTGGACACACC | 13855 |
rs258196741 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61579295 | AAACTGAAGGCTCTG[C/T]CGCTGAGGTGTGAGG | 13855 |
rs258323021 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61578098 | GACTACCCAGTGAGA[G/T]CCTGTCACAAACATA | 13855 |
rs258364526 | in-del | -/GTGTGTGTGTATGTATGTGTGTGT | | | intron-variant | Epn2 | Mm_Celera | 11:61524249 | AAATCAGGTAAAGGG[-/GTGTGTGTGTATGTATGTGTGTGT]GTGTGTGTGTGTGTT | 13855 |
rs258375014 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61545184 | ACCCTGAAGGTTGAT[A/T]AGGAAGATAGCAAGT | 13855 |
rs258401618 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61573858 | ACCCATCTCTGGGTG[C/T]TCACAACCACCTTTA | 13855 |
rs258429114 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61555224 | CTGTAGAGCAGACTA[A/G]CCTCCAACTCAGAGA | 13855 |
rs258482646 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61569064 | CAGAACTGGCACCCA[C/T]AAGCCCCATCTAGAA | 13855 |
rs258553413 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562980 | CTTGATTCTATTCCA[C/T]TTCTGTGAGTTCCAG | 13855 |
rs258617601 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61561568 | CCTGAAGCATCTTAA[C/T]ATGTCTCCCAAGAGA | 13855 |
rs258636100 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575242 | CTCAAAGAGGCATGC[-/T]TTTTTCCCCCCCTTT | 13855 |
rs258681850 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558068 | TAAAAGAGTTTGCCT[A/G]CATGTACACACATGT | 13855 |
rs258725731 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575956 | ATTCCCAGCAACCAC[A/G]GGGGCTCACAACCAT | 13855 |
rs258775619 | snp | A/G | | | upstream-variant-2KB | Epn2 | GRCm38.p3 | 11:61581235 | ACCTGGGTCTCAAAA[A/G]CAGGGAATTTAGAGT | 13855 |
rs258924157 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61524039 | TTTAAATGTTAACCC[C/T]GTGTGTAGATTTTTC | 13855 |
rs258952037 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61530070 | ATGTGTGTCTGAGCG[C/T]AACAATACACAATGT | 13855 |
rs259010717 | snp | C/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61542507 | CAGTAAGGCCTCCTA[C/G]TCCAGCTCTGCCAAC | 13855 |
rs259162176 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61525846 | CCACCTGGTGCTTCC[-/A]AAATTTCAAACATGT | 13855 |
rs259170069 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61562702 | ACAGAAGTAACTCCC[A/G]AGTTGTCTTTCTGAC | 13855 |
rs259205443 | in-del | -/AAAAAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61565353 | ACACCAGCTCTCCTG[-/AAAAAA]AAAAAAAAAAAAAGC | 13855 |
rs259229649 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61563317 | AGCAGGCAGAATTCG[A/G]GTGATCAGGAGTGAC | 13855 |
rs259255864 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61577142 | GTTACACAGTGAGAC[C/T]CTTTGGGGAATAAAT | 13855 |
rs259387313 | in-del | -/TCT | | | intron-variant | Epn2 | GRCm38.p3 | 11:61575992 | TGGGACCTGATGCCC[-/TCT]TCTTCTTCTTCCTCC | 13855 |
rs259431200 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61560892 | AACAAAACACTACCA[A/T]GGCATATGGATATTG | 13855 |
rs259572450 | snp | C/T | | | intron-variant | Epn2 | Mm_Celera | 11:61520343 | CTATAATACTCTGAC[C/T]CACTCTAGGGGTTAT | 13855 |
rs259746975 | in-del | -/A | | | intron-variant | Epn2 | GRCm38.p3 | 11:61555234 | ACTAGCCTCCAACTC[-/A]AGAGATCCACCTTCC | 13855 |
rs259876275 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61568403 | GCAGACCCCACCCCA[C/T]ATGCAATAGCATCCT | 13855 |
rs259906464 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61538218 | GCTACCAGAAGACCT[A/G]TCTCAGTAAGACAAA | 13855 |
rs259952235 | in-del | -/AAA | | | intron-variant | Epn2 | GRCm38.p3 | 11:61532494 | ACAGGCAAGCCCAGG[-/AAA]AAAAAAAAAAGCAAT | 13855 |
rs259970340 | snp | A/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61537174 | AACGTCACACTGGCA[A/T]GGAGTGTTCACTCAG | 13855 |
rs260066847 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61527229 | CACAAAAGAAACACC[C/T]CACTGCAAGGTCAAC | 13855 |
rs260085732 | snp | C/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61553803 | GGCTCTTGCCTAGAG[C/T]CATTCCCACAACTGC | 13855 |
rs260099652 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61559331 | CTGAGATTTAAGGAG[G/T]GAGTATGGCACTACC | 13855 |
rs260158818 | snp | G/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61536864 | TACCTACCTACCTTT[G/T]GGTTGATTTTATTCC | 13855 |
rs260163076 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61572636 | TCTCCAGACCCACAC[A/G]AAAAGCTCAGCACAG | 13855 |
rs260180156 | snp | A/G | | | intron-variant | Epn2 | GRCm38.p3 | 11:61523230 | TTCAGAACAGGGGCT[A/G]GAGAGTATTAAAGAG | 13855 |
rs260213679 | in-del | -/T | | | intron-variant | Epn2 | GRCm38.p3 | 11:61558773 | CAGCAATATATAGCC[-/T]TTTTATGTCTGGATT | 13855 |