| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs48777203 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108374690 | CCGAAGACACTGAGG[A/C]GCCATCCATAACGCA | 68519 |
| rs48784581 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108483570 | GGAAATGTTTTATTT[C/T]TTTTTTTTCTTCTTC | 68519 |
| rs48798437 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml1 | GRCm38.p3 | 12:108393740 | GAAGACTCAAGCAGT[A/G]TAACTACACCAAAGA | 68519 |
| rs48801144 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404019 | GTTTGCAGGGAGCGC[A/G]CAGGTCAGCCTCTAA | 68519 |
| rs48801276 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108507007 | TACACTCCCACACTG[C/T]TGTTCATCACCAAAG | 68519 |
| rs48807222 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108386772 | CCGGAGACTTTGCTG[A/C]AGTGGCTTGTTACAG | 68519 |
| rs48809560 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | GRCm38.p3 | 12:108411296 | TCTGGTTGGCCATGA[C/T]GACTGTGTTGTATTC | 68519 |
| rs48835784 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108446030 | AAAGACTCTGATACC[C/G]TCTTCTGGTTGCCAA | 68519 |
| rs48851070 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108413069 | ACATAAGTGGGACAC[A/C]TGTGTCTGTGGAGTC | 68519 |
| rs48877490 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448508 | CCCGGAAAATAGCCA[C/T]GAGTCACATTTGTCA | 68519 |
| rs48878214 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108462466 | CTGGCGGAGTGAAGA[C/T]GCCATGGCAGCAGGT | 68519 |
| rs48882313 | snp | C/T | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108415148 | GGCTCTGATGTTAGC[C/T]GATCGTCTCAGTGGT | 68519 |
| rs48900727 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108448496 | CATTTCAGGGTACCC[A/G]GAAAATAGCCATGAG | 68519 |
| rs48909358 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108378235 | TTTAACCAATCAGTG[A/G]CTACCCAGGCAGTGC | 68519 |
| rs48927934 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108379852 | ATGAGCCAGGGTCTA[C/T]GCTGTAATCCAGGCT | 68519 |
| rs48930105 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535392 | GGGGTCGTGGGGGGG[A/G]GGGGAGTGGGATGTG | 68519 |
| rs48943747 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml1 | Mm_Celera | 12:108385809 | AAAGAAGGATAAATG[C/T]TCTGCCCTTTATCTG | 68519 |
| rs48959334 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Eml1 | Mm_Celera | 12:108384376 | TGCCCCACAACCAGA[A/G]TAGGCTGAGCAACAC | 68519 |
| rs48959541 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500704 | CTAACCTAAAACTTT[C/T]GATCAACTCTCCTAA | 68519 |
| rs48960002 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | Mm_Celera | 12:108414208 | ATTGGTTATCACAGA[C/T]TTAGAGTTTTGTGTC | 68519 |
| rs48986974 | snp | C/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413244 | AGCACAGGGTTGGGG[C/G]CAGAAATCAGTGGCA | 68519 |
| rs48996189 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml1 | Mm_Celera | 12:108386454 | TTGCCAGTGGACATC[A/G]TTGCTTGGAGCTGCA | 68519 |
| rs48997033 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108456177 | CCAGGCTAACCAAGA[C/T]AGTTACGGTTTATTT | 68519 |
| rs49018563 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108401513 | CAGGACTTGCCACAT[C/T]AGTCACAGGAAATGC | 68519 |
| rs49026785 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410439 | ATCCATGGAGGGAGC[A/G]CACCTCTCAGGACCA | 68519 |
| rs49030381 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412299 | AGATGGGAAGTGGGG[A/G]CAAGCCCAAAGAACA | 68519 |
| rs49040840 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108399058 | ACACGAGAGCTGCCA[C/G]CCGAGAGCCCAGTGT | 68519 |
| rs49045003 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108444216 | AAGTGTTGGGATTAA[C/T]GACATTGTGCTACCA | 68519 |
| rs49050990 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460793 | ACAGTCAGGACTACA[A/C]AGAGAAATCCTGGGA | 68519 |
| rs49054886 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108374726 | TTCCTCCAGGCCCAC[A/G]AGAGACCCGGTTGCT | 68519 |
| rs49070954 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500802 | TCCATAAAATCCTTA[A/G]TTCATCTAGACAGCA | 68519 |
| rs49078135 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108385192 | CACCCAGCTCAGCAC[C/T]CAGGCTTTTCAAAGG | 68519 |
| rs49082214 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108481707 | ATTTATTCACTTTAT[A/G]TCTCAATATCAGCAC | 68519 |
| rs49082247 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108388025 | AGGCATTAAAGTCTG[C/T]AGGAGTTAGGTGGGT | 68519 |
| rs49083093 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108388051 | TGGGTTCAGGCCTCA[A/G]AACCCATCTGGCTCC | 68519 |
| rs49099323 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Eml1 | Mm_Celera | 12:108380839 | AGCCGTGAAAAGGAC[A/G]GAAAGCCAGCCATTT | 68519 |
| rs49100248 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108419001 | TGCCACACCACATCT[C/T]CAGTCCGCTAGAACA | 68519 |
| rs49114248 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108380227 | CTGCACATTAATCCT[C/T]GGTTAGATGTATACA | 68519 |
| rs49114250 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108376774 | CTTTAAATGATCACT[A/G]CAGTTGTGGTGAACA | 68519 |
| rs49119037 | snp | C/G | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108420930 | ATTTCTGCAAAGTAT[C/G]GAGGAGAGAGCATAA | 68519 |
| rs49131881 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108380805 | AAGAGGGGTGGGCTA[C/T]TATGATAGAATGTTA | 68519 |
| rs49132938 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449518 | ACAGCTGACACCTGA[A/T]AGAAGTTTGTGAAGT | 68519 |
| rs49145996 | snp | C/T | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108414079 | GTTTACACATCGACG[C/T]GTTGTGTAGGAATAT | 68519 |
| rs49187114 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108421003 | AGTGCACACTGGCAT[C/T]AAATCTGTCCCTTCG | 68519 |
| rs49197011 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418969 | GGCCTCAGGCTTGCT[C/T]AGCAAGCACACTTTA | 68519 |
| rs49208240 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108389636 | AATATGGAGAGACCA[A/G]TATATATGTTTTTTG | 68519 |
| rs49224478 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108376975 | CAGGGGGAAACTGAG[C/G]CCAAGAGAGAAAGAA | 68519 |
| rs49233480 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108459006 | CCTGCTGCCATGCTC[C/T]CCACCATGACAGACA | 68519 |
| rs49235361 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430871 | GGCCGCTGGTGGTCA[C/T]CCTTCTTTATTCTGC | 68519 |
| rs49247407 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108395239 | CTCCCAAAGTCCTGA[C/T]GCTTCCTCAATAAAA | 68519 |
| rs49261487 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500715 | CTTTTGATCAACTCT[C/T]CTAATTTCCTAACTT | 68519 |
| rs49285920 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108530188 | CTGTGGGGGAGGGGG[C/T]TTCTTGAGTAAGAGC | 68519 |
| rs49286173 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430859 | CGTGTTCTCCTAGGC[C/T]GCTGGTGGTCATCCT | 68519 |
| rs49291589 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108458968 | CCAGCGCTATGCCTG[A/C]CTGCCTGCCTGCCTG | 68519 |
| rs49319006 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462925 | TGGGCCTGTGCTCTG[C/T]ATCTGAAGCTCTGAG | 68519 |
| rs49333853 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108392838 | GCTTCCTGCACGGGG[C/T]CAGGAACAACAGGCT | 68519 |
| rs49348990 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433813 | TGGGCTTCTTTCCTG[C/T]TTCAGTGGAATAAAA | 68519 |
| rs49356066 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430818 | TTCTTTAAAAACACA[C/T]GTGGAGTGGAAAACC | 68519 |
| rs49370346 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108384911 | CCAGCCGTGGCTCAG[G/T]CAGTGGGACCTGAGG | 68519 |
| rs49381671 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml1 | Mm_Celera | 12:108380465 | CCAATAAGTGAGACC[A/G]TAGGCCTAACTATGT | 68519 |
| rs49387219 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108483700 | CGAGCTGTGTGTGCA[A/G]AGCAGGGTGTCTTGG | 68519 |
| rs49397083 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446373 | TGACAAGAGCCATGT[C/G]TTTGCCTTCAGATGT | 68519 |
| rs49405528 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108529442 | GCACTTGAGTACAAA[A/C]GCCCACACACACTCT | 68519 |
| rs49406245 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108378481 | GGGATACTTCCATAC[C/T]GACCCGGGTCCAGAG | 68519 |
| rs49407406 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452559 | CTCTGAGGAACTTCG[C/T]TCCTAACCACAACTC | 68519 |
| rs49410128 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445988 | GCACCGGCATGGAGG[C/T]TCCCAACTGTCTGTA | 68519 |
| rs49417802 | snp | A/G | 0.497778 | 0.0332592 | intron-variant, downstream-variant-500B | Eml1, Gm33385 | GRCm38.p3 | 12:108400191 | CTGGGTAGGGTGCAG[A/G]AAGCCATGGTTCCAC | 68519 |
| rs49421170 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108389931 | TCTCTGTCCTCCCTA[C/T]CCCCAGGTTCTCTTC | 68519 |
| rs49423420 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443167 | GAGACCTATGAAAGA[A/G]TAAATGTTTCTCTTT | 68519 |
| rs49424647 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108417028 | TGGGAGTGTATTGTG[C/T]ATGATGGGAAACTGT | 68519 |
| rs49425508 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Eml1 | Mm_Celera | 12:108380600 | GCAGGTATCGCATGG[C/T]GATCGATCGTATGCT | 68519 |
| rs49464942 | snp | A/G | 0.497778 | 0.0332592 | intron-variant, missense | Eml1, Gm33385 | GRCm38.p3 | 12:108401250 | TCCGAATATCCTGAA[A/G]AGATAGATGCTCATC | 68519 |
| rs49468948 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml1 | GRCm38.p3 | 12:108381963 | CAGAGTCGGGGTCCA[C/T]GGTGAACATCTTCAC | 68519 |
| rs49469449 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | Mm_Celera | 12:108414474 | GACTCAAGTGTTCAC[A/G]TGGAAGGCAATGGTT | 68519 |
| rs49470069 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499754 | CAGATCCATCCATTT[C/T]CTGTAAACTTTATTT | 68519 |
| rs49474187 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108381672 | CAGGACCAGCAAGAA[A/G]CAACAGAGCTAGGGG | 68519 |
| rs49476422 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml1 | GRCm38.p3 | 12:108385836 | TCTGGCTCATTTTGC[A/G]CTTGTCACCCGAGGG | 68519 |
| rs49486070 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433501 | ATTGGATGGAGTTGG[G/T]CTCTCTCTCTCTCTC | 68519 |
| rs49489206 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108389851 | AGGGTGGGATACTGC[A/G]GCCCCATGGCCTCTA | 68519 |
| rs49491891 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Eml1 | GRCm38.p3 | 12:108385106 | AAGCTTGTGAACAGG[C/T]CTGGAGATTCTACTG | 68519 |
| rs49492373 | snp | C/T | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108413480 | AAGGAGATGGCAATG[C/T]CTCTCTGTAAATGGA | 68519 |
| rs49519871 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108401600 | GCCCAAGATTAGGTA[C/T]GCCTCCTCACAGACC | 68519 |
| rs49521110 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Eml1 | GRCm38.p3 | 12:108395050 | TTAATGAGAAAAAAA[A/T]ATATATCAGAGTTGA | 68519 |
| rs49524226 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108388453 | GCTCACTATAGACAG[A/G]AACACAGCTGCAGCT | 68519 |
| rs49524231 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108376068 | CTGCCTAGTCAGGTA[A/G]CTGCAATCAGGATTT | 68519 |
| rs49527205 | snp | A/G | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108420825 | CTGGGCATTCCACTC[A/G]GGGCCTCACGCTTGG | 68519 |
| rs49529948 | snp | A/C | 0.32 | 0.24 | intron-variant, missense | Eml1, Gm33385 | Mm_Celera | 12:108401311 | GCTGATGTGACTGAT[A/C]CAAGGAACAGGCTTT | 68519 |
| rs49534359 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Eml1 | Mm_Celera | 12:108377243 | TCCTGAAGAATGCCA[A/G]CCCAGCCTGTCCTGT | 68519 |
| rs49540007 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443121 | GCCCGGTCTACACCG[A/C]AAGTTTCCAGCAGAG | 68519 |
| rs49541061 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108384306 | ACCAGGGAGGTACCC[C/G]CAAAGCTCCAGCCAT | 68519 |
| rs49569950 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108395131 | AATCATTGTCTTGGG[A/T]TTCATGGGTAACGTT | 68519 |
| rs49593090 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108378324 | TTGGGTGTCACTGAC[A/G]GCACTGAAAGCCCAC | 68519 |
| rs49597180 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408375 | CCCATCAACCCCTGT[C/T]CCTGCTTTAATGTGT | 68519 |
| rs49608261 | snp | G/T | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422434 | GGGTGTGCTACTGAC[G/T]CTTGGGTTTGCTTTT | 68519 |
| rs49617261 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108507585 | AATGCTTCTGCCTCA[C/G]TCTCCTGAATGCTGG | 68519 |
| rs49625864 | snp | C/T | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108414168 | CCTTTATCCCATAAC[C/T]TCATTCAGGTGCAGT | 68519 |
| rs49626577 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml1 | Mm_Celera | 12:108377682 | AGAGAGCAAGATGTT[C/T]TATTTGTTTGGATTT | 68519 |
| rs49647922 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108385465 | TCAGAGGAAACAAAA[C/T]GGATGGCCAGGAACA | 68519 |
| rs49653347 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518258 | CGTGAGCACATACAT[A/G]CATGCAGACAAACAT | 68519 |
| rs49660457 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108535316 | TGTGCCTACGTAAGA[C/T]CTGGGAGGAGGGAGG | 68519 |
| rs49667467 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108397834 | AGTAAGTATAAACCC[A/G]GGGCTCGAACACTGC | 68519 |
| rs49682502 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449866 | ACCCACGTAGCCGCC[A/G]TCTCGCTAGCCAGCC | 68519 |
| rs49684471 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108463337 | CGTGGCAAGCCCATA[A/G]AGCGTGCGTGATGCT | 68519 |
| rs49686237 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108495215 | TTCCTGTCTGGCTCC[A/C]GCATCCCGTTCCTAT | 68519 |
| rs49687488 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499878 | GACGAAGGTGGATCC[A/T]GTGCTTACAAGGGCT | 68519 |
| rs49689377 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535590 | ATAGAAAGTTCAGAT[A/G]CCAGTGGGGGGCAGA | 68519 |
| rs49697211 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108393205 | CTCATCCTTGGTTGG[C/T]TCCCAGAGTTGGTGC | 68519 |
| rs49701864 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402260 | CCTAACACCACCTAA[A/C]GCTTTGATGAAATGT | 68519 |
| rs49710780 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Eml1 | GRCm38.p3 | 12:108375348 | AAAAACTACATTTCT[A/G]GAGTAATCTTTAGGA | 68519 |
| rs49716083 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446017 | TAACTCCAGGCCCAA[A/G]GACTCTGATACCGTC | 68519 |
| rs49716354 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108469592 | ACATCTTGGTTCCTT[A/C]TAGTTTTTGACAATT | 68519 |
| rs49739434 | snp | A/C | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108394821 | GTGATTCTGAACCAT[A/C]TAACCAGCTAGGGCC | 68519 |
| rs49742225 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108499318 | CTAGTTTTATGTCAA[C/T]TTGCCATAGCTGAAG | 68519 |
| rs49757771 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108388160 | GGCTCAGTCCCGGGT[A/G]TTAAGGCTTTCAGTC | 68519 |
| rs49771152 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402344 | ATGTGCAGAGATGCA[C/T]TGAGATACCCGAGTA | 68519 |
| rs49775099 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108421017 | TTAAATCTGTCCCTT[C/T]GGAAACTAGCTCCCT | 68519 |
| rs49776750 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | Mm_Celera | 12:108396957 | CAATTCTTTATGTGT[G/T]TTCCCGGGTGACTTC | 68519 |
| rs49781501 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108390368 | ACACAAAAATGTACA[C/G]TTTAGGGTTTCTGAG | 68519 |
| rs49800104 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108395752 | TCTGGCATTAGCCAC[A/G]ATGCACAGAGAGAGA | 68519 |
| rs49803311 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108439320 | TCCAACTCCCAGAGA[A/T]CCTTTTGTAGTTTTT | 68519 |
| rs49808976 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml1 | GRCm38.p3 | 12:108384369 | CCAGCTCTGCCCCAC[A/G]ACCAGAGTAGGCTGA | 68519 |
| rs49814121 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml1 | GRCm38.p3 | 12:108390404 | TAGATGGATAAAGGG[C/T]TTGAGTTTAATCCTT | 68519 |
| rs49817184 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449503 | CGAAAGGGTCTTTAG[A/G]CAGCTGACACCTGAA | 68519 |
| rs49821854 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108380124 | GAGTTACAGGTAGTT[G/T]TGAACTCCCTGATGA | 68519 |
| rs49831994 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413437 | AACTGTGTGTGTATA[C/T]GCAATCAGCAGCCCT | 68519 |
| rs49839774 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108379493 | GGTGATGGCTTTCCG[C/T]TATTTCTGCATTGCT | 68519 |
| rs49847026 | snp | A/G | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108421471 | CAACCATGGTTCACT[A/G]TGATCCCTTTGCCAG | 68519 |
| rs49847580 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502133 | CAGAGTGAGGGAGGC[A/G]GAGATGGGGACCCTC | 68519 |
| rs49857455 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108495014 | TTCTGTGTGGGTGCT[A/G]GGGATCTGGACCCTG | 68519 |
| rs49870866 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108387155 | CTGGGTGCCAGGTTC[A/G]TTCTCTGCCCCTGGT | 68519 |
| rs49885439 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108453652 | CCCCGCAGAAGACAG[C/T]CATCACTCTTTCCAG | 68519 |
| rs49905545 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108524031 | CAGATATTTATAGAA[A/C]ATTTCATCCTAAAGC | 68519 |
| rs49907599 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449488 | TCAGCCCTGTGTCCT[C/G]GAAAGGGTCTTTAGA | 68519 |
| rs49917505 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446171 | ATAAAATCTCATTGT[A/G]TAGTTCAGATTAGGT | 68519 |
| rs49938671 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108500280 | TCATTGATCAGTAAA[A/G]TTTAAACAAGCCAAG | 68519 |
| rs49947692 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Eml1 | GRCm38.p3 | 12:108377863 | GCTTGGAGGAAGCAC[A/C]TTTACCCACTGAGAC | 68519 |
| rs49955288 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108448037 | GTACAAATGGTGGAT[A/G]CAAGTCTGAGATTCC | 68519 |
| rs49956876 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108373549 | AGGTCATCGTCTGCT[C/G]TAGGGTCTAGCAGAG | 68519 |
| rs49962557 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108386937 | TGGAGGTGAAGGGAC[G/T]TAATCAGCCTGTCAC | 68519 |
| rs49967252 | snp | A/C | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108413421 | CACATAACCAAGGGT[A/C]AACTGTGTGTGTATA | 68519 |
| rs49967286 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374270 | GTTCAAATCTCTGCT[C/T]CCACTCACTGGCTCT | 68519 |
| rs49972384 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403802 | AGCAACTCCAGCACA[C/T]GATGCCCCCAAACCA | 68519 |
| rs49974042 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108388661 | GAATGATGTATCTCA[C/T]AGCTGCATCACATCC | 68519 |
| rs49981292 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Eml1 | Mm_Celera | 12:108380983 | AGTGTAGCATGGTGC[G/T]TACCAAAGGGTGGAG | 68519 |
| rs49984446 | snp | A/G/T | 0.495868 | 0.0452663 | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411515 | TAAAAACCTTTAAAA[A/G/T]CCCCACTGGGATAGT | 68519 |
| rs49984714 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500084 | TCATAGCCACAGTTA[C/G]AAATTTTCCAGAGAT | 68519 |
| rs50029983 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108417496 | TCAGTCCTGGAGCAA[C/T]GGCACCAACAGGGCA | 68519 |
| rs50049753 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108458078 | AGCCTCTGCTTGCAA[A/G]AGCTCAGCTTACTCT | 68519 |
| rs50051604 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449537 | AGTTTGTGAAGTTCC[A/G]GCTTCCTTCCTCCTG | 68519 |
| rs50094401 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443147 | CAGAGCCAGCCATAC[A/G]TAGTGAGACCTATGA | 68519 |
| rs50094945 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108379918 | AAAATCACAGCACTC[C/G]TCTTGCCCCATCGCT | 68519 |
| rs50101566 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | Mm_Celera | 12:108397417 | GCTCAGTTGCTGCTG[C/T]GTTCAGGACTGTGGA | 68519 |
| rs50124562 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108458567 | GATAATAAAGAAAGT[A/T]AAATGTTATGGGACG | 68519 |
| rs50126277 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108415243 | ATAGTCTCAAGATGA[A/G]CTTGTCCCTTTGAGA | 68519 |
| rs50130292 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108373576 | AGAGGCTGGACCCAG[A/C]ACCCCTATTCTCTGT | 68519 |
| rs50149051 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500705 | TAACCTAAAACTTTT[G/T]ATCAACTCTCCTAAT | 68519 |
| rs50149307 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108502044 | GGGTAAGACACATCG[C/T]GTGGCTGAGAATGTG | 68519 |
| rs50157089 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108483670 | TGTCCTGAAAGAGCC[A/G]TGATGGATTATACCC | 68519 |
| rs50167717 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446051 | TGGTTGCCAAGGTAA[C/T]CAGGCGTGCACACGG | 68519 |
| rs50172171 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108412907 | TGCTATAGTTTATGT[A/G]TGCATTCTTCCAACT | 68519 |
| rs50194533 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412658 | AGACTCACTTAGAAC[A/G]TATAGCATGTGAAGC | 68519 |
| rs50201209 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449417 | CACCGAGTTGCACAG[C/T]GTGCCTGCTTGTGAT | 68519 |
| rs50202955 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449529 | CTGAAAGAAGTTTGT[A/G]AAGTTCCGGCTTCCT | 68519 |
| rs50206688 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108377463 | CGCCATGTGTAGGGC[C/T]CATACAGGCTCAGTG | 68519 |
| rs50212239 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108535688 | AGGCAGGGAGGAGAG[A/G]TAGCCAGTTCCAGGA | 68519 |
| rs50224053 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108396270 | TATTCATAGACTGGC[C/T]CATCAATTATGCATT | 68519 |
| rs50227967 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446130 | TGTAAAAGCAAATGC[A/G]TTTATTTATGTAAGC | 68519 |
| rs50240742 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377434 | ACAAATAACTGCGTG[C/T]GTGTGCCCTCCCTCG | 68519 |
| rs50244409 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108405143 | CTAAGAGCACACCTT[A/G]GGGTTCCCTGTAGCT | 68519 |
| rs50277378 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499349 | TCATCAGAGAGGAGG[A/G]AACCTCAAATAAGAA | 68519 |
| rs50305973 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108374515 | CTCTGGATACTCTCG[C/T]TGGGGGAGGGTTGCT | 68519 |
| rs50326829 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500630 | GCTCGCTGTGCCTCT[C/T]TCTCTAACTTGAGCG | 68519 |
| rs50342505 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108501083 | AGTAGGACGGTGGGC[A/G]GTCTCCAGGGAGCTC | 68519 |
| rs50348029 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Eml1 | GRCm38.p3 | 12:108417179 | CGTCAGAGATATGTA[C/T]GCAATTGCAGGGGAT | 68519 |
| rs50382295 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464277 | GCCATTATTTCATGC[C/T]CCTCCCAGGACACAG | 68519 |
| rs50407453 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Eml1 | GRCm38.p3 | 12:108374885 | AGCTGTGCAGACCTC[A/G]GAGGACAAACCTGAC | 68519 |
| rs50426091 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108387756 | GGAGAACTGAGGTCC[C/T]TTCAGATCAGCGCTC | 68519 |
| rs50435416 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108375926 | CTAGGCCACATCCCT[C/T]TAAGGGACACTCAAG | 68519 |
| rs50443811 | snp | A/C | 0.497778 | 0.0332592 | intron-variant, synonymous-codon | Eml1, Gm33385 | GRCm38.p3 | 12:108411015 | ACCATGCATGGAGAC[A/C]AGGAAGGGCTTGGTC | 68519 |
| rs50455240 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108502203 | GGTTCCGTGAGAGAC[C/T]CTGCCTGCATATGTG | 68519 |
| rs50460809 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108374296 | GCTCTGTGGCCTTGG[A/G]CAAGACACTTACCTG | 68519 |
| rs50466974 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Eml1 | GRCm38.p3 | 12:108417764 | AGCCACAGTGTAATG[C/T]TCCCTATTGATGCTA | 68519 |
| rs50471799 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml1 | GRCm38.p3 | 12:108392257 | GCCACAGTGGCATGC[A/G]TGATCCTTGTGGGCC | 68519 |
| rs50472859 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500299 | AAACAAGCCAAGTCT[A/T]TGGTTGCAAGTTTTT | 68519 |
| rs50495803 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Eml1 | GRCm38.p3 | 12:108375117 | GGCTCACAACAGCAA[A/G]AGGAGGTGTCATGTC | 68519 |
| rs50496932 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108397682 | ACCTGGCCATCTTCA[C/T]CCCCAATCACATGTG | 68519 |
| rs50516961 | snp | C/T | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108422280 | TCAGAATTTTACCTC[C/T]AGTGGACAGAACCCA | 68519 |
| rs50526325 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108458282 | ACTTTCAGAGTCACC[A/G]CTCCAAGGACAGAAC | 68519 |
| rs50539729 | snp | C/T | 0.495868 | 0.0452663 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108413537 | TTGGTGCGGAGTCCC[C/T]AGGATAGGTACAAGC | 68519 |
| rs50550937 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml1 | GRCm38.p3 | 12:108379561 | TCATGGCTGTCTGAA[C/T]GCCCTCTTTTGAGAA | 68519 |
| rs50558739 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108376001 | TCTCTGGGCCCTGAG[A/G]CTCTAATTCAGGCTG | 68519 |
| rs50581241 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108483198 | AAGTTTGGGGTCACG[C/T]GCAGGGACAGACAAG | 68519 |
| rs50593966 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445978 | TCGATTCCCAGCACC[C/G]GCATGGAGGTTCCCA | 68519 |
| rs50595684 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108378817 | GCCAATCATTCAAAG[C/G]AAGGGGCGAGAATTT | 68519 |
| rs50617519 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Eml1 | GRCm38.p3 | 12:108386575 | TTAGAAAGGGCATCA[A/G]GGAAGGTGCTGATGG | 68519 |
| rs50633163 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml1 | Mm_Celera | 12:108385973 | TGTTCTCCTGTGCAA[C/T]GTTGGATGCTGTACA | 68519 |
| rs50633411 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458722 | GTATCTTCTTCAGTG[A/G]CTCTCTGCTTTATAT | 68519 |
| rs50640243 | snp | C/T | 0.489796 | 0.070696 | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | GRCm38.p3 | 12:108401028 | GCCCGCAGGGCTCAC[C/T]TTGCTGTGTTGACTA | 68519 |
| rs50640921 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108458719 | TGGGTATCTTCTTCA[A/G]TGACTCTCTGCTTTA | 68519 |
| rs50645414 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eml1 | GRCm38.p3 | 12:108389420 | CTATAGGCATGGAGA[A/C]TGCTTTGTGCACTCA | 68519 |
| rs50645892 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108435202 | CTTACTTATGTCTGA[A/G]TTCTAAGATGTCTTA | 68519 |
| rs50646997 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108401561 | GCCAAGATACTGTGC[C/T]TGGAGAGCTGAGACT | 68519 |
| rs50666295 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458656 | AAATGTTAAATCTCA[A/G]TAAGTAGTGTGTGTG | 68519 |
| rs50678277 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Eml1 | Mm_Celera | 12:108386584 | GCATCAAGGAAGGTG[C/T]TGATGGATGTGGCCC | 68519 |
| rs50679415 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108499594 | TGAGGGAAGTCCGGG[A/C]AGGAACTCAAGTAGG | 68519 |
| rs50698174 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409437 | ACTGTGGTGCTCCCA[C/T]ACCTTCTTCTGGGGC | 68519 |
| rs50742983 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml1 | GRCm38.p3 | 12:108386542 | TGCATGGAGGCATGT[A/G]TGTGTACAAAAATCC | 68519 |
| rs50750995 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499879 | ACGAAGGTGGATCCT[A/G]TGCTTACAAGGGCTG | 68519 |
| rs50753431 | snp | C/T | 0.165289 | 0.235211 | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108410060 | AATTTAGTGTACATG[C/T]GTGCACACTTGCACA | 68519 |
| rs50765398 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108394382 | ACACTAAAAATAATT[A/T]AAATTTTTAATTTAC | 68519 |
| rs50802808 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml1 | Mm_Celera | 12:108400083 | TGTCTGTCCATTCTG[C/T]CGGACAGAAAGCAGG | 68519 |
| rs50812999 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108376045 | TTTCATGGCTTCCTG[A/C]TGTCCCTCTGCCTAG | 68519 |
| rs50814246 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383968 | CTGCAAGAAGCAATC[C/T]TGAGATGAAGTGTCT | 68519 |
| rs50834841 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108380344 | TACAGCTTACTAATC[C/T]TCCAGAGTACTTCAC | 68519 |
| rs50841985 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108483351 | AAATAAAGGACATTG[G/T]TTTCCCTTGCTGTCC | 68519 |
| rs50842410 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405816 | GCTAATGTCCTCTGA[A/T]TTGCTCTGAAGTTGG | 68519 |
| rs50864003 | snp | C/T | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108414153 | TTTAGCCACCATGGG[C/T]CTTTATCCCATAACT | 68519 |
| rs50876142 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108379374 | TACAAAGGCTCTTGA[C/T]TTTGAACTTGGGGTT | 68519 |
| rs50882991 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Eml1 | Mm_Celera | 12:108378758 | ACATTGTGTAAACCG[C/T]GGCTAGCAGACGGGT | 68519 |
| rs50884696 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108444227 | TTAATGACATTGTGC[C/T]ACCATAGCCAGACAG | 68519 |
| rs50886773 | snp | A/C | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108400830 | AGAAAAAAATGTTTC[A/C]TGACAAAGTCAAACA | 68519 |
| rs50903031 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml1 | Mm_Celera | 12:108416221 | ATTTCATATTAATAT[C/T]GGTGCTGAGAAAAGC | 68519 |
| rs50906146 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Eml1 | GRCm38.p3 | 12:108379492 | AGGTGATGGCTTTCC[A/G]TTATTTCTGCATTGC | 68519 |
| rs50922848 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108501953 | AATGGCTGTAGTGTG[C/G]AGCTGCGGAGCTCTG | 68519 |
| rs50926971 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458755 | TGAGACAGTCTTCGT[G/T]GTGGTTTCATAGTTT | 68519 |
| rs50928129 | snp | C/G | | | stop-lost, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538228 | GTGGCGAGTCATTTA[C/G]TCCCTGTGGGAGCCC | 68519 |
| rs50945353 | snp | C/T | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108421503 | GTCTCCCAGTTCTTG[C/T]CACTACAACTGCCAG | 68519 |
| rs50951004 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108378393 | GTTCGTAGTGGTACA[A/G]GGTCTTCATTCATGC | 68519 |
| rs50955746 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108397708 | ATGTGAGAGTCACCA[C/G]TGCTAGTAAGGTCCT | 68519 |
| rs50964173 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Eml1 | GRCm38.p3 | 12:108380609 | GCATGGCGATCGATC[A/G]TATGCTGTCCTGGAG | 68519 |
| rs50975196 | snp | A/T | | | intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108537745 | cacacacacacacac[A/T]cTCTCTGCCTACCTA | 68519 |
| rs50978183 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108414877 | TTTCTGATAAAAATC[C/T]AGATCTCTAGTAACT | 68519 |
| rs50981032 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108417429 | ACAAAGTCTATGTCC[C/T]CATGTAATGGTGGGT | 68519 |
| rs50991052 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Eml1 | GRCm38.p3 | 12:108386597 | TGCTGATGGATGTGG[C/T]CCAGCCCCGGGTGAT | 68519 |
| rs51010894 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108435934 | AAAACATAATCATGG[C/G]AAGACACATGTGACA | 68519 |
| rs51019101 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433580 | ATCCCTGTTGGGACG[C/G]CTAAGCAATAGCACT | 68519 |
| rs51022492 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449405 | GAACCATGAAGTCAC[C/T]GAGTTGCACAGTGTG | 68519 |
| rs51031194 | snp | C/T | 0.391111 | 0.206368 | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | GRCm38.p3 | 12:108400981 | AAAAATAAGAGCAGG[C/T]TGAGCAGGGCAGGGC | 68519 |
| rs51040646 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108451854 | GTAGATGTGATACTG[C/T]TTTTATGAGAGGCTC | 68519 |
| rs51043688 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108410951 | CACTCCTATTCTTCA[C/T]CTGGACCTACCTGGG | 68519 |
| rs51066370 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Eml1 | GRCm38.p3 | 12:108387294 | TCTGTACTTCTCCTG[A/G]CACTTGTCATGTGTG | 68519 |
| rs51067272 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml1 | Mm_Celera | 12:108415620 | ATTGCCTTCCGTTTT[C/T]CAATTCACCTCAGAT | 68519 |
| rs51073199 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448532 | TTTGTCAGAGGTGTA[C/T]AAAGGCAAAAACCAC | 68519 |
| rs51073214 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443035 | ATATGTATGCCAAAG[A/G]ATTGCTTAAAAAAAT | 68519 |
| rs51078667 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108397765 | TCTCACTAACTTACT[G/T]CATGGCTGGGCAGCT | 68519 |
| rs51093952 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108375159 | GGCCCCAAAGACAAC[C/G]GAGGAGCCATTTGCG | 68519 |
| rs51094935 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108379540 | CTGAGGGTGTTTGCA[C/T]ATACCTCATGGCTGT | 68519 |
| rs51105827 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433658 | CATAGTGAAACGCAC[G/T]CGGCTGCCGCTCCCC | 68519 |
| rs51120355 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448528 | CACATTTGTCAGAGG[C/T]GTACAAAGGCAAAAA | 68519 |
| rs51142545 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374346 | GTTAGAGAGCATGTG[G/T]GGGGGGACTCTGTTT | 68519 |
| rs51158290 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108410790 | GCTTTACTGACGGCC[A/G]GGAGGACATGAGAGG | 68519 |
| rs51171847 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506991 | AAGGGTTTATTCAGC[G/T]TACACTCCCACACTG | 68519 |
| rs51182703 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Eml1 | Mm_Celera | 12:108393441 | AAGAGGCAGAATAAG[A/G]CACCAAGCCCCTCAC | 68519 |
| rs51192564 | snp | C/T | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108395027 | ATAGGAAGTGTGCTG[C/T]TTAGCATTTAATGAG | 68519 |
| rs51193604 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500122 | ATAAAAACGCTCTTC[A/G]AAAATCCAAATCTTT | 68519 |
| rs51198874 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430741 | TTCCCACACCCATTC[C/T]CCACCTGCAAAAAAA | 68519 |
| rs51205829 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108394971 | AAAATTCTCACACAT[A/G]TTCAGAGGCAATGAG | 68519 |
| rs51236678 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108378446 | AGGTAGATCCAGTCC[C/T]TTACACAGAAGCATC | 68519 |
| rs51247070 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374228 | TACAATATCAGAGAG[C/T]AAGGAAAGTAGTCTA | 68519 |
| rs51255921 | snp | A/T | 0.495868 | 0.0452663 | intron-variant, missense | Eml1, Gm33385 | GRCm38.p3 | 12:108411003 | GGGAGCCTCTGAACC[A/T]TGCATGGAGACAAGG | 68519 |
| rs51257277 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108388517 | ATGTCTGGAAGGAGC[G/T]CACATTCTTCCCTAG | 68519 |
| rs51272563 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535620 | AAAGGCAGTGTGCAG[A/G]GAGGAAGTTACACAT | 68519 |
| rs51281303 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458752 | TTTTGAGACAGTCTT[C/T]GTTGTGGTTTCATAG | 68519 |
| rs51293080 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108385602 | TCATATGCTATTAGG[C/T]TTGGCCATTTGCTTC | 68519 |
| rs51306470 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | Mm_Celera | 12:108398129 | GCTCCAAGCCAGTGT[A/G]GCTTCACTGACCTAA | 68519 |
| rs51308092 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108377615 | AGCATACAGGGGAGC[C/T]GTTAGATATTCAATA | 68519 |
| rs51319926 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430988 | AGGCCCAGCCCACCA[C/T]GACCCAAGCCTGGGG | 68519 |
| rs51327214 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108392597 | ACCTTGTACTTGGGA[G/T]ATATAAAACTCCACA | 68519 |
| rs51328983 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108387726 | ATAAAGTAATGTGTG[C/T]TCAAAGACCGAGCTG | 68519 |
| rs51341210 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108506961 | CATCATGACTAAGAA[G/T]CAAGTTGGGGAGGAA | 68519 |
| rs51357396 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449520 | AGCTGACACCTGAAA[A/G]AAGTTTGTGAAGTTC | 68519 |
| rs51362755 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108388572 | CTCCATCCTTGCCCA[C/T]GATACCTGCCTCTTC | 68519 |
| rs51366635 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412980 | ATTTATTTTTTTTCT[A/G]CTGCTTTAAATGGCA | 68519 |
| rs51373083 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108376136 | ACCAGGAGGGACCCG[A/G]ATGTTTGATGTGCTG | 68519 |
| rs51373846 | snp | A/G | 0.489796 | 0.070696 | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108413197 | CCCTGATATTGATAG[A/G]CTATGTTTAGCCATC | 68519 |
| rs51395601 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404062 | GGCGCTGGCTTCTCC[A/G]GGAAGCAAAGGCCAA | 68519 |
| rs51396875 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml1 | Mm_Celera | 12:108389814 | GCAGAGAGAGAGCCC[A/G]CTAGTAGGCAGTGCG | 68519 |
| rs51401760 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108394314 | TCCCCTAATGTCAGC[A/G]ATCTTCACTCTTAAG | 68519 |
| rs51415480 | snp | C/T | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108377324 | TGACGCCCTCATTAT[C/T]CTGCGTTCTGGCGTA | 68519 |
| rs51419837 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | Mm_Celera | 12:108385026 | GACCCAAGAGCACCC[C/T]GTTTGTGTCTGTTGA | 68519 |
| rs51423859 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108444222 | TGGGATTAATGACAT[G/T]GTGCTACCATAGCCA | 68519 |
| rs51433723 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108374829 | GACTTGAGTTTCTCC[C/T]TGGAGACTCCTCAAA | 68519 |
| rs51436491 | snp | C/G | 0.497778 | 0.0332592 | intron-variant, missense | Eml1, Gm33385 | GRCm38.p3 | 12:108411139 | GATTCTGGGGCCAGG[C/G]AACTCTGTCCAGTTC | 68519 |
| rs51436824 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108436047 | CTCGTTCCAAGGGAA[A/T]ACTCTGAAAAGTCCC | 68519 |
| rs51447193 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108405424 | CTGTAGAGCTGATGG[A/T]GCTGCCTTGGAAGAA | 68519 |
| rs51487044 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Eml1 | Mm_Celera | 12:108397470 | TTTCTGCCTGCAACT[C/G]TCCGCCTCTGTCATG | 68519 |
| rs51492715 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108420784 | GGACTGCCAGTGGGA[A/G]CTACCACACCTAGTT | 68519 |
| rs51493291 | snp | C/G | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108414928 | CTGCTGCTTCGAGAT[C/G]GCATTTTAAATATGC | 68519 |
| rs51495566 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108483751 | CCTGAAGTTTTTACA[A/G]CACTTTCCCACTGGA | 68519 |
| rs51502446 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108399203 | CTGAGCGTCCTGAGT[A/G]TCCTTTTCTCCTACA | 68519 |
| rs51521052 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml1 | Mm_Celera | 12:108398843 | ATCAGCTGCAAAACG[A/G]AGCCTTGAACCAGAC | 68519 |
| rs51527841 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108377775 | TGTATGTGTGGTGCT[C/T]AGGAGACAGCTTGTC | 68519 |
| rs51534768 | snp | A/T | 0.5 | 0 | intron-variant | Eml1 | GRCm38.p3 | 12:108384885 | GTGGGAGGTAGGGAG[A/T]CTGAGAAATACCAGC | 68519 |
| rs51542294 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108462467 | TGGCGGAGTGAAGAT[A/G]CCATGGCAGCAGGTA | 68519 |
| rs51550922 | snp | A/C | 0.444444 | 0.157135 | intron-variant, missense | Eml1, Gm33385 | GRCm38.p3 | 12:108411095 | GGCTCGGCAATGTGC[A/C]AAGGGTGGACTGGGA | 68519 |
| rs51553465 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108377352 | GTAGGCCTCTTTCTC[C/T]TTCTGGATTCGGGTA | 68519 |
| rs51580227 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Eml1 | Mm_Celera | 12:108399668 | TGACTCCCCAGCAAG[A/C]GCTATGTCTAGGGTT | 68519 |
| rs51615415 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108405545 | CACTGTATTTACTTA[C/T]TTACTTATTTTAAGT | 68519 |
| rs51628078 | snp | C/T | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422445 | TGACTCTTGGGTTTG[C/T]TTTTTACAATATTCC | 68519 |
| rs51650734 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374329 | GGGTGAACATTTGTC[C/T]TGTTAGAGAGCATGT | 68519 |
| rs51657309 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535484 | TTTCTCATGATCCAC[A/G]GTAGTATTTTCTGAC | 68519 |
| rs51663938 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458565 | TAGATAATAAAGAAA[C/G]TTAAATGTTATGGGA | 68519 |
| rs51665185 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500749 | ATTTTCTATCAACTA[A/C/T]CCTAACTTCCCAAAA | 68519 |
| rs51667873 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421665 | CTAGAGCACTGACAA[A/C]ACACTGGGTTGTTTG | 68519 |
| rs51668588 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml1 | GRCm38.p3 | 12:108377027 | ACCGTTCTCAGGGCG[C/T]TTGCTCTCTCTAACA | 68519 |
| rs51679686 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500325 | TTTTTCCTTCTGGTT[G/T]GCTGGCGACAACCTA | 68519 |
| rs51693075 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500716 | TTTTGATCAACTCTC[C/T]TAATTTCCTAACTTT | 68519 |
| rs51698116 | snp | C/G | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Eml1, Gm33385 | GRCm38.p3 | 12:108400403 | TGACTCTCATGCCAA[C/G]TATGAATAGGAGAGT | 68519 |
| rs51699254 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108385452 | TCCTCTGAGACCATC[A/G]GAGGAAACAAAATGG | 68519 |
| rs51710121 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108381429 | TGGCACACATTAAAT[A/C]ACATGTAAAGTAGTT | 68519 |
| rs51718279 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml1 | GRCm38.p3 | 12:108396689 | CCCCGATTCTAGCAG[A/G]ACCATGAGGAAGAGA | 68519 |
| rs51721146 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108377693 | TGTTCTATTTGTTTG[A/G]ATTTATTATATCTTG | 68519 |
| rs51744111 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Eml1 | GRCm38.p3 | 12:108395319 | AGGACAGGATCGCTC[C/T]CTCTCCTCCGCCCCA | 68519 |
| rs51755046 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108399588 | ATGCCTTCTGTGATG[C/T]TTACATGACCACTGA | 68519 |
| rs51760212 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446143 | GCGTTTATTTATGTA[A/T]GCATTTATTTAGATA | 68519 |
| rs51770261 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml1 | Mm_Celera | 12:108415902 | AGGACATTTGAACTC[A/G]GGATGGGAGTCACCA | 68519 |
| rs51782303 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108445979 | CGATTCCCAGCACCG[A/G]CATGGAGGTTCCCAA | 68519 |
| rs51785786 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108382670 | AGTGGGAAAGTGTAA[A/G]TATTGGAACAGTTGC | 68519 |
| rs51805439 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108388551 | GCTTTGTCCCGGGAA[C/T]AGCAGCTCCATCCTT | 68519 |
| rs51810062 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108461629 | CTGGCTTGCTCAGCC[C/T]GCTCTCTTATAGAAC | 68519 |
| rs51826060 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108481854 | GCCCAGTTAGGAGAA[C/T]GGGATCCAGAATCTG | 68519 |
| rs51834789 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108416956 | TGGACCATGCTACGT[A/G]TCTAGGTACCCAAAT | 68519 |
| rs51856684 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108394939 | CCATGAACACACACT[C/T]ATATGCGTATACACT | 68519 |
| rs51883585 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108381936 | ATAGACACAATTGCA[C/T]ACAATCCACAGCAGA | 68519 |
| rs51893342 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108395695 | AGATTCATATGTTTT[C/T]TAGGTCATTAAGAAA | 68519 |
| rs51899876 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108376033 | TTGCCTTCTGGGTTT[C/G]ATGGCTTCCTGATGT | 68519 |
| rs51906871 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108430982 | GGCTGAAGGCCCAGC[C/G]CACCACGACCCAAGC | 68519 |
| rs51928605 | snp | A/G | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Eml1, Gm33385 | GRCm38.p3 | 12:108400302 | TGGGCTGTCACATGC[A/G]GTTCTAATGCCACCA | 68519 |
| rs51939910 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108533395 | CCTGGCCCTGCTCAG[A/C]GGCAGCAGGGTAGAT | 68519 |
| rs51956934 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Eml1 | Mm_Celera | 12:108399755 | GGCAAGCGGACCTGC[C/T]CACAGGATTCTGGTT | 68519 |
| rs51959775 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381283 | ATTGTTATTAAGGAT[A/C]GCATACTGCGTACAT | 68519 |
| rs51962555 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108381248 | AAGAAGTACATTCCA[A/G]ATCTGTGAACCCCAA | 68519 |
| rs51973025 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108375415 | GGCTAGGTTATCTAT[C/T]CTCTGCAGGATGTCT | 68519 |
| rs51985169 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108413847 | GCTATACCATAAGCA[A/G]TACAATGCAATTAAG | 68519 |
| rs51989864 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408429 | CTGTGTGTCTGTGTA[A/G]CTTGGTGTTAAGTAG | 68519 |
| rs51997793 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446249 | CATTTCACTGACCAT[A/G]AGGTCATTAATATGT | 68519 |
| rs52033451 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108415303 | CCCATGGTGCCTACG[G/T]TATTGTATGTGGGAT | 68519 |
| rs52036786 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108458249 | ACACGGAACACACAC[A/G]TAATTTTCTGTGAAG | 68519 |
| rs52039770 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108385101 | AAAGAAAGCTTGTGA[A/G]CAGGTCTGGAGATTC | 68519 |
| rs52054521 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108381842 | GGGGTGTCACACCAG[A/G]GAGCTCAGAAGGGAA | 68519 |
| rs52057264 | snp | C/T | 0.32 | 0.24 | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402245 | TAGATGAGATGCTGC[C/T]CTAACACCACCTAAA | 68519 |
| rs52060290 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446219 | CCTCCACCACCAGAA[C/T]GCACTTCAAGATTCC | 68519 |
| rs52091142 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108378018 | ACAATGTAAAGGAGC[C/T]AGTTCCCTTCATCTA | 68519 |
| rs52223897 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108384618 | CTCAGACACTGGGAT[A/C]AGCACATTTAAACAG | 68519 |
| rs52235593 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108405007 | ATCCTAGGTGATTAA[C/G]TAAAACTCCACTTTA | 68519 |
| rs52251639 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | GRCm38.p3 | 12:108379946 | GCTGAGATTATAGGC[A/G]TGAACCATGACATTT | 68519 |
| rs52251874 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Eml1 | GRCm38.p3 | 12:108380033 | TCCTCTTTCCTCTTC[C/G]TATGTCTGAGTGTAT | 68519 |
| rs52269725 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml1 | Mm_Celera | 12:108381191 | AGCTGGGAGAGGGGC[A/G]TGGAGGACCGTGGAC | 68519 |
| rs52311027 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108439189 | TGCTGAGCCAGCACT[C/T]TGTGTTCCAGCCCCA | 68519 |
| rs52351221 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494877 | GTGTGTGTGTGTGTG[C/T]GTGTGTGCGTGCACA | 68519 |
| rs52390153 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml1 | GRCm38.p3 | 12:108391025 | CTACATAGACTGATA[A/G]GCACATACACACACC | 68519 |
| rs52403099 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403192 | AATTACCATCCTACC[G/T]TCTTTATCTTTTTTG | 68519 |
| rs52410139 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Eml1 | Mm_Celera | 12:108384638 | CATTTAAACAGACAG[A/G]CAAACAGGATAAAAC | 68519 |
| rs52424803 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml1 | GRCm38.p3 | 12:108387818 | TTGAGACAGAGCTCT[A/G]AGGAGAAACAGAAAG | 68519 |
| rs52474701 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml1 | Mm_Celera | 12:108380071 | TACATGAGGGGGTGC[C/T]TAAGGCAGCCAGGAA | 68519 |
| rs52587955 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eml1 | GRCm38.p3 | 12:108379120 | GGCTCCTCTGTATGT[A/C]GCCTTTCAACTTTTA | 68519 |
| rs52598723 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108448195 | TGTCTGGGAATATGC[A/G]CAGATGTGTAGGTAC | 68519 |
| rs52600513 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108439178 | GGCTCTGGGTATGCT[A/G]AGCCAGCACTCTGTG | 68519 |
| rs52603893 | snp | A/C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381082 | GCTCAGGGAGTGGGG[A/C/G]CGGGCTCGGGGCGGG | 68519 |
| rs52605503 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466697 | TGTGTGTGTGTGTGT[A/G]GTGTGTGTGTGTGTG | 68519 |
| rs52609023 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381102 | CTCGGGGCGGGGTTC[A/G]GGGTTCAGGGCGGAG | 68519 |
| rs52615136 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108391095 | acagacagacagaca[C/G]acacacaCCCCAATG | 68519 |
| rs52617818 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449679 | TGTGAGTGTGTGTGC[A/G]TGTGTATGAATGTGT | 68519 |
| rs52618713 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108434570 | TAGTTGGAGTCCTGT[A/G]ATTGAATCTTAAGAA | 68519 |
| rs52619152 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449742 | GTGTTTCGCATGACG[G/T]GGAACATTGATGGAG | 68519 |
| rs52620935 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108448199 | TGGGAATATGCACAG[A/G]TGTGTAGGTACCCAT | 68519 |
| rs52627163 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108466710 | GTGGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 68519 |
| rs52627430 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449733 | AGCATGTGTGTGTTT[C/T]GCATGACGTGGAACA | 68519 |
| rs52629446 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433912 | GGTTGGCATTTGGAA[A/G]ATAGGAACCATGTTC | 68519 |
| rs52631266 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381183 | GCACAGGGAGCTGGG[A/G]GAGGGGCATGGAGGA | 68519 |
| rs52632814 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108515741 | TTGAGACAGGGTTTC[C/T]CAGTATAGCCCTAGC | 68519 |
| rs52637596 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108384588 | CAACCCTATCAGGTG[G/T]CACTGGTGCATAAGC | 68519 |
| rs52639691 | snp | A/C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381083 | CTCAGGGAGTGGGGC[A/C/G]GGGCTCGGGGCGGGG | 68519 |
| rs52652338 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108466709 | TGTGGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 68519 |
| rs52725135 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471491 | GGAAGAGCAGGGGAG[A/G]AAGAGCAGGGAGGGG | 68519 |
| rs107610395 | snp | A/G | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108370071 | TAGCTATCTTTAGTC[A/G]CACCAGAAGAGGGTG | 68519 |
| rs107649935 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108481633 | TCTATAAGAGTCCCA[A/G]GTCTGCCTGGACTGA | 68519 |
| rs107662786 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108394483 | CAATCTAAAGGAGTC[A/G]TTGCTTTCCACTCAG | 68519 |
| rs107695062 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448850 | AATCTGGCCCTGACA[G/T]AGGGTTGTGTGTAGT | 68519 |
| rs107797181 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448927 | TACTGATTCTCCACT[A/T]GTACCCGTGAACTGC | 68519 |
| rs107824687 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108448791 | TAATAACCTCCAACA[C/G]TCCAGGAAGCGTCTG | 68519 |
| rs107841505 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108448014 | AGGCGAGAGCTAGGG[C/T]TGAAGTGGTACAAAT | 68519 |
| rs107861954 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108448968 | GACATGCACCACCAC[A/G]TATGGTTTCTGTAGT | 68519 |
| rs107997285 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108384688 | GACAAAAACCCTGGG[G/T]CTAGTTAGATAGTTG | 68519 |
| rs108131858 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108462382 | CTATGAGAAAACACC[A/G]TGCTCAAGGTAACTT | 68519 |
| rs108156776 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449044 | ACCAGCTGAGCCACA[A/T]CTGCAGTTCTTGCTT | 68519 |
| rs108406779 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108459065 | GCCTCCAATTAAATG[C/T]TCCCTCTTATAAGTT | 68519 |
| rs108422891 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384694 | AACCCTGGGGCTAGT[G/T]AGATAGTTGTCAGGA | 68519 |
| rs108449837 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108493606 | GAGATGGTCCCCCCA[A/G]GCGATGCTAGATCAA | 68519 |
| rs108473201 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108459346 | AAAACCTCATGATTT[A/G]GGATGAGTGCTTGTC | 68519 |
| rs108500525 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448611 | ACATACTTCCTGCCC[G/T]CATATCTCCTGCCTA | 68519 |
| rs108509212 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108448592 | GGGGCAAGTATATAT[C/T]CTGACATACTTCCTG | 68519 |
| rs108533681 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500540 | CCATCCTAGGGTGTA[C/T]GCTCACTTTGATCGT | 68519 |
| rs108551107 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376046 | TTCATGGCTTCCTGA[C/T]GTCCCTCTGCCTAGT | 68519 |
| rs108639057 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108448565 | GGTCACACTCCCCAT[A/C]GGGTTCAATCAGGGG | 68519 |
| rs108709952 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108384681 | CCAAACTGACAAAAA[A/C]CCTGGGGCTAGTTAG | 68519 |
| rs108729574 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108459007 | CTGCTGCCATGCTCT[C/T]CACCATGACAGACAT | 68519 |
| rs108822796 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108459243 | TCCAAACTGAGGTCC[A/T]TACGCTTGTCCTGCA | 68519 |
| rs108927326 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108448896 | AATCATCTTAGAGCC[A/G]AGGATGGCCTTGATC | 68519 |
| rs211706562 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108373324 | AAAACTTGTAGCACC[A/G]TTAAAATGATGCCAG | 68519 |
| rs211712649 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108466973 | CAGGCAGTTGGTGGT[A/G]AGCCACCCAACGTGG | 68519 |
| rs211717192 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379762 | TTTCCTGCCTCTGCC[C/T]CCCCAGTGCTGGGAC | 68519 |
| rs211719070 | in-del | -/TGTTTGTTTAATG | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406933 | GTTTAGTGTCTGCCT[-/TGTTTGTTTAATG]TGTTTGTTTAATGTA | 68519 |
| rs211733145 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108518463 | GCAGTGCCCTGAGAC[C/T]GGTGGGGGTGGGGCA | 68519 |
| rs211747286 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504748 | TGGGTTAGGGGGCGT[-/G]GGGGGAAACAGAAGT | 68519 |
| rs211756382 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108466086 | CCCTTTCTTCATAAG[A/C]GGCTTTTTGTCAGGG | 68519 |
| rs211759176 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108430267 | TCACTTCAGTCAGCA[C/G]AAAGTATATGTCCTC | 68519 |
| rs211769275 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108526226 | AGCTGTTGGCACCCC[A/G]GCTGTGAATGCATCG | 68519 |
| rs211796807 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108429462 | GGAGGAACCACCTGG[A/G]CACTGAGGCATCTCC | 68519 |
| rs211807102 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517980 | TCTGATTTACATAGA[A/G]AGTTCTAAGACAGCC | 68519 |
| rs211831877 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108384720 | CAGGAGAGTGTCTAT[A/G]GTGCAAGCATGGGGA | 68519 |
| rs211836459 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474183 | TGATTGTGTCAAGTT[A/G]ATAATTAAAACTCAC | 68519 |
| rs211839435 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108420149 | TTTGCTTTTTTTTTT[A/T]ACCCAAATTTTATAA | 68519 |
| rs211844145 | in-del | -/AA | | | intron-variant | Eml1 | Mm_Celera | 12:108429723 | TGCTTGGAGTGGGGG[-/AA]AAAAAACCCTAAATT | 68519 |
| rs211847624 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525769 | TAACAAAGTAAGTTC[C/T]AGGATAGCCAGGACT | 68519 |
| rs211856594 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433445 | ATTACATAACAAGAA[-/T]TTTAACACTCCTAAG | 68519 |
| rs211867584 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108481270 | TGGGGGTGGGTGAGG[A/G]TGGGGAGTGAGCAGA | 68519 |
| rs211921815 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108441943 | AGACTATGCAGCTAC[A/G]GGGACTAGTATATCA | 68519 |
| rs211938967 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532381 | TCAGTGCTCTTAACT[A/G]CTAGGCCACCTCTCC | 68519 |
| rs211949545 | in-del | -/ACAC | | | intron-variant | Eml1 | Mm_Celera | 12:108482438 | CACACACACACACAT[-/ACAC]ACACACACACACAGC | 68519 |
| rs211956521 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108390253 | AGGGTTGGTGAGTAA[C/T]CCTGCCTCAAAACCT | 68519 |
| rs211963116 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108488013 | TCTAGTGGTGGGCTC[C/T]AGAGCTCCCAAGCCC | 68519 |
| rs211972275 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447367 | ACCCAAACTAGTACA[C/T]GGTCTGGAAGGATGC | 68519 |
| rs211975107 | in-del | -/CA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473205 | ACATACATACCACAC[-/CA]CACACACACACACAC | 68519 |
| rs211981672 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108441603 | TGGGTCCTTCCCCAG[C/T]CCAAGGCTCACCTTA | 68519 |
| rs212003072 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108496007 | AAGACTGCAGTGTTG[A/T]CTGGACGCCCAAGAA | 68519 |
| rs212024848 | in-del | -/TTTTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108515698 | CGCACAGATCAGACC[-/TTTTTT]TTTTTTTTTTTTTTT | 68519 |
| rs212063806 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446914 | CCTCAGGGGGTCACT[A/G]TCCTAGCAAAGATGA | 68519 |
| rs212068901 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404088 | GCCAATCCATCATCC[C/T]AGGGCTTTACCCTGA | 68519 |
| rs212073427 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379156 | GTTTTGTATAgtgtg[C/T]gtgtgcgtgtgtgtg | 68519 |
| rs212081900 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532066 | ACTTAAACCTTCCAT[-/G]TCCTAAGGGCCCAGG | 68519 |
| rs212091526 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108495061 | GGCAGTCACTTTAAT[A/G]ACCTAGACACCTCCC | 68519 |
| rs212098266 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108386193 | ACTGTCATCTGGTGT[C/T]TCTGCCTGGACCCCA | 68519 |
| rs212100009 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108527188 | CGTTGGGTTTGGTCT[A/C]GGGCACTTGGGATCT | 68519 |
| rs212109341 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108393557 | GGGAGTGGCGCTGTG[C/T]TGGGGACACCTCGGA | 68519 |
| rs212125802 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108437410 | GCCATGGCTGAGTTA[A/C]AAGATCTCACCCAGG | 68519 |
| rs212127868 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108443197 | TATGATTTATTGTTG[A/G]TGAATGTTGGCTTTC | 68519 |
| rs212139255 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108533214 | CTGAGCCCTGTCTCA[A/G]ACATTTGATGTGTGT | 68519 |
| rs212145428 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108487185 | ACTCAGATTCAAGGC[C/T]ATTATATGCTATGCA | 68519 |
| rs212175244 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108491113 | GAACAGATGGCCCAC[A/G]CCATGATCCTCCCAG | 68519 |
| rs212179472 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392958 | GGTCCCTGCTGGCAG[C/T]CGAAGGGAGGCATGA | 68519 |
| rs212187013 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442873 | TCCTTCAGCATTGGC[A/T]ATGACTAAAGTCAAA | 68519 |
| rs212236256 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108453725 | AGGGTGACGGTGCTC[C/T]GGACCTTCTGACTGC | 68519 |
| rs212238271 | snp | C/T | | | intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108537794 | TCACTCAAGCTCTGC[C/T]GAGCTGACCAACCCC | 68519 |
| rs212239848 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108399846 | ATTTCTCCATCCAGT[C/T]TCCCCTCTCCAACAG | 68519 |
| rs212250360 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108448053 | CAAGTCTGAGATTCC[A/G]TGGTCCAGCGCCACA | 68519 |
| rs212263783 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108503383 | AACATTCACTTGAAC[A/G]GGCTTCGACATGCGG | 68519 |
| rs212303411 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405529 | AGCATTAAAACAGGA[A/G]CACTGTATTTACTTA | 68519 |
| rs212305592 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108497722 | TAGCAGCATTTAAGG[A/G]GTGATTAAAGTGACC | 68519 |
| rs212324372 | in-del | -/GTCT | | | intron-variant | Eml1 | Mm_Celera | 12:108431453 | CCTTGCTAACCACCA[-/GTCT]AAGTAAAATCCAGGT | 68519 |
| rs212341752 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108497021 | AGTTTAGATTCCCAA[A/C]ACTCATAAAAAGAAC | 68519 |
| rs212342086 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108454644 | TCATTTATTTATTTT[A/G]TGACAGGGTCTCATT | 68519 |
| rs212364533 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503951 | GCCTTTTAAGCCTGC[C/T]TTTGTGGTCACCAAG | 68519 |
| rs212400532 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108510848 | CAGTCTGGCTTGGAA[A/G]GAAGGAGGTGAGGAA | 68519 |
| rs212403211 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461557 | AACTCAAGCAGGTCA[G/T]AAAGCAGGAGCTGAT | 68519 |
| rs212414811 | snp | A/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413662 | CTGTACATCATGTGT[A/G]TGACTGGTGCCCTCA | 68519 |
| rs212427065 | in-del | -/GCCATTAT | | | intron-variant | Eml1 | Mm_Celera | 12:108520773 | GCACTGAGATTAAAG[-/GCCATTAT]GCCCTGCTAAAACTT | 68519 |
| rs212447776 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm33385 | Mm_Celera | 12:108400373 | GAGTCTTTACCACCC[A/G]TGGATTGTGTGGGAT | 68519 |
| rs212478210 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421037 | ACTAGCTCCCTTACA[A/G]ATGCAGAGGAGCCAC | 68519 |
| rs212489927 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108448761 | CATGCGACTTCTTAT[A/T]TCCCATAAACAATAT | 68519 |
| rs212513261 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388904 | AGAGAGCTGGTCTCT[C/T]CTCTTTCCTAATGCT | 68519 |
| rs212517459 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108396562 | GTCACCCCACAGGTC[A/G]CAGCTGCCAACCAGA | 68519 |
| rs212524154 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406172 | CCCCTCCTTCCCTCT[C/T]CCTCCCCCTCCTTTC | 68519 |
| rs212531905 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108385983 | TGCAATGTTGGATGC[-/T]GTACAGCCGAGATCT | 68519 |
| rs212537954 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455074 | TGCATGTGTGTGCAT[G/T]TGTGTGTGTGCGTGT | 68519 |
| rs212543442 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451260 | TCCGTTTAACATTGT[A/G]TCCCGCAGACACACA | 68519 |
| rs212567231 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504582 | GAGGTGATTTCCTGT[A/G]GGGTTTGGCACAGGT | 68519 |
| rs212582357 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108395751 | CTCTGGCATTAGCCA[A/C]GATGCACAGAGAGAG | 68519 |
| rs212583327 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402846 | CGGCTTTATGTCCCT[A/G]CCTCCTCCAGCATCC | 68519 |
| rs212621642 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108459974 | GAGGGAGGCTGGGTG[A/G]GGACACACTCCTTGT | 68519 |
| rs212624810 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108493562 | AGAAACGTTCTCACA[A/C]GCTAACCCAATTCAG | 68519 |
| rs212647745 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410357 | ATGCACCTGGAGCCC[C/T]GACTTGACTGGCACC | 68519 |
| rs212656048 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458222 | CCTGTGCATCATGGC[A/G]TCTGGCTCGAGACAC | 68519 |
| rs212701297 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450997 | GGAGACCCCAAACAG[A/T]AAATGACCAGGGGAA | 68519 |
| rs212765960 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108515451 | GAAAGGTTTTTTAAG[G/T]TTAGGATACAATGAT | 68519 |
| rs212808013 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369250 | GAGCAGGAGCAGTGG[A/G]CCCCTGAGATGCCTC | 68519 |
| rs212821710 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108416807 | CCACCATCAATATCA[A/T]TAATAAAGTCAATGA | 68519 |
| rs212829332 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440377 | CGGAGACATTCAAGT[C/T]CGAGAACTGGCAAGG | 68519 |
| rs212861932 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108453350 | GGTCTTCATGTTTCT[G/T]TTGTTGTTTGTTTTG | 68519 |
| rs212877598 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108425163 | CCATTCAGTTAATTA[C/T]AATGACAATGATTCG | 68519 |
| rs212881758 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108485864 | TGAAGAAGCACTTTT[C/T]TCCTCCGACTTTTTT | 68519 |
| rs212883918 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108502589 | GAGACAGGCAGCAGG[C/T]ATAGCGACTAGACCC | 68519 |
| rs212907091 | snp | C/G | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108535943 | TCTAGTGTGCGCACA[C/G]ACACCTGTAATAAGG | 68519 |
| rs212915170 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108412090 | CCGACTGGGACCAGT[C/T]TCTAACTCCCAAGCA | 68519 |
| rs212929280 | in-del | -/TTTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108510996 | GGACAGGAACCTCCA[-/TTTTT]TTTTTTTTTATCAAT | 68519 |
| rs212939527 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108464594 | AAGCAGAGGCAGGTG[A/G]AGCTCTGTGACTTCT | 68519 |
| rs212957601 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108380827 | AGAATGTTAGTCAGC[C/T]GTGAAAAGGACAGAA | 68519 |
| rs212971907 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508696 | TGCCTCAAGCACAGC[C/T]TGAGAGCATTTGCCT | 68519 |
| rs213033054 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108483797 | GGTGGTTTAAGCACA[-/C]CTGGCTGCTCTTGCA | 68519 |
| rs213034417 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465162 | GGGATTAAAGGCGTG[C/T]GCCACCACTGCTCGG | 68519 |
| rs213038297 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419188 | TGGCTTAGTCACTCA[A/G]CATAATGTTCTCAAA | 68519 |
| rs213049804 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108434922 | ATACACACATTATAC[A/C]TGCCAGCTCTTGTCT | 68519 |
| rs213050410 | in-del | -/GTTCAGGACTGTGGAACCTGAAGTCAAACAAGGTGG | | | intron-variant | Eml1 | Mm_Celera | 12:108397418 | CTCAGTTGCTGCTGT[lengthTooLong]CTTTCTGCCTGCAAC | 68519 |
| rs213057636 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108371735 | CATTAAGCTGGGACA[A/T]TCTCGTAGGTCCTGG | 68519 |
| rs213080911 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378119 | ATTTTTTTAAAAGAA[A/T]GTTATTAGCATTTTG | 68519 |
| rs213104294 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108418177 | ATGTGGGAGGAACTC[C/T]GCGCTACCTGTAGAT | 68519 |
| rs213117793 | snp | C/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409482 | GCCCAAAGTCACTTA[C/G]AGTTCATTCCTCAGT | 68519 |
| rs213118208 | snp | A/C | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | GRCm38.p3 | 12:108411339 | TTGTCTCCCTCCCCC[A/C]ACTCCCATGTATACC | 68519 |
| rs213121918 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464436 | TGGCTCAACTTTCGC[C/T]AGAGTTGATTTTCTG | 68519 |
| rs213125874 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472723 | AGCTCTAGGTTCACC[C/T]GAGAGACCCTGCCTC | 68519 |
| rs213136902 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383873 | ATCTTCATGTTGATC[C/T]CTAGGAAGTCTGCTC | 68519 |
| rs213164654 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524608 | AGCCGCTTGACAGCA[C/T]ACCTGAACGCTCTAG | 68519 |
| rs213171443 | snp | A/G | | | missense | Eml1 | Mm_Celera | 12:108471963 | GGGGCCAGGAAAGAA[A/G]TAGTTGTGCCGGTAA | 68519 |
| rs213176970 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478020 | TGAACAGAGAGTGGG[-/T]TATCACCTACAGATG | 68519 |
| rs213177290 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507023 | TGTTCATCACCAAAG[A/G]AAGTCAGGACAGGAA | 68519 |
| rs213187239 | in-del | -/ACAT | | | intron-variant | Eml1 | Mm_Celera | 12:108510482 | TGGTTGGGATGGCAC[-/ACAT]ACATCTTTAACGCCA | 68519 |
| rs213192992 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108502019 | GGCAGTGCTGGGGAG[-/A]TGGCTCAGCGGGTAA | 68519 |
| rs213197907 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524299 | CAAAACAGGCCTCAA[C/G]GGATACAAGAAGAAT | 68519 |
| rs213204564 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108463160 | GGTCAAGTAGCACCA[A/G]TGGATAAAGGCAAGA | 68519 |
| rs213220923 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479341 | CTCTTAATATGGTCA[G/T]TACGTTGTTTGATTT | 68519 |
| rs213226080 | in-del | -/AAAAGAAAACATC | | | intron-variant | Eml1 | Mm_Celera | 12:108467301 | GGAATAATAGCAAGA[-/AAAAGAAAACATC]AAAAACCATTGTCTG | 68519 |
| rs213242569 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108514763 | GCAAGGAGCCTGCAT[A/G]TGGGCACTGGTTGCT | 68519 |
| rs213248327 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108389459 | TTATAACTACTATAC[A/G]ACAAGGTCACCTAGT | 68519 |
| rs213248660 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108440863 | CCTCGTACTTCTCCA[C/G]CTCGGCCTGCAGCCT | 68519 |
| rs213262485 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108434694 | TCATACTACACACAC[-/AT]ACATACATACACACA | 68519 |
| rs213266726 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486260 | GGTGAGGGGCTCTCA[A/G]TGAAGCCTGTAACAG | 68519 |
| rs213292407 | in-del | -/TA | | | intron-variant | Eml1 | Mm_Celera | 12:108379147 | TTTAAAAATGTTTTG[-/TA]TAGTGTGCGTGTGCG | 68519 |
| rs213315485 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108505607 | ATATTTTACACTTAT[A/T]TAACAAGGCGATTTA | 68519 |
| rs213352132 | in-del | -/GGAG | | | intron-variant | Eml1 | Mm_Celera | 12:108531968 | ATAGGAAGAAGAAAA[-/GGAG]GGAGGGAGGGAGGGA | 68519 |
| rs213373702 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108375334 | CAAGATAATCTTTTA[A/T]AAACTACATTTCTGG | 68519 |
| rs213400917 | in-del | -/GTATTGAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108442227 | AAAACCACCAAAAAT[-/GTATTGAAA]GTCAAATTCATGATG | 68519 |
| rs213401767 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527859 | CTCCCTGGGGCGGGG[A/G]CAGTGCATGGCAGCT | 68519 |
| rs213404548 | in-del | -/TC | | | intron-variant | Eml1 | Mm_Celera | 12:108467390 | CCATGTGTAGCACAT[-/TC]TCTCTATGTGTGGGC | 68519 |
| rs213405131 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455251 | CTGTGTTTTCTGGAT[A/C]AGCACTAGGTGTCAG | 68519 |
| rs213406127 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504659 | CTCCGATCTGCGAGA[A/G]CATCAGAACAGAGAC | 68519 |
| rs213420493 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469032 | AGGACAAGAGGACAA[C/T]CAAGGCTGACAGTGC | 68519 |
| rs213440270 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458780 | TAGTTTCACATATTG[A/G]AATATTTGATCCCCA | 68519 |
| rs213444783 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108414593 | TGGATTCACAACACT[A/G]GACTCAGAAGCTCCT | 68519 |
| rs213460708 | in-del | -/CAGGG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108493110 | ATGTGTCTCTCTTCT[-/CAGGG]ACTGCCCAAGTTTTG | 68519 |
| rs213464040 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461686 | CACCCACAAGGGGAC[C/T]TCCCCCCTTGATCTC | 68519 |
| rs213479710 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108380759 | AAAATCCTTGCCCAG[A/C]ATGATGATTACATTG | 68519 |
| rs213500533 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108476430 | AAGCTTCTCCCCTGT[A/G]CTGTTTTCGAGGGCT | 68519 |
| rs213502393 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108467919 | GTACCTTGTATCAAA[C/T]AGTGCTTTCTAGAGG | 68519 |
| rs213511783 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108475123 | GCTAGGATCATCCAT[G/T]GTTTATAACAACACA | 68519 |
| rs213533546 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108430836 | GGAGTGGAAAACCAT[A/C]TGTTTGCCGTGTTCT | 68519 |
| rs213551183 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527013 | CAGCTAACTGCTTTG[A/G]CCTAACAAAACTTGG | 68519 |
| rs213598679 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392804 | GTTGATCTCTCTCTC[C/T]CGAGGAGGAGGAGGT | 68519 |
| rs213605823 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519157 | GACATCACACATGCG[A/G]AGTTCAACTCTGTAA | 68519 |
| rs213622742 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474823 | TGCAGCCGGGTGATG[A/G]TGGCACCAGCCTTTA | 68519 |
| rs213630580 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108416155 | AGAGAGGGTCGTCAT[C/T]CCCCTCCCCCAAAAG | 68519 |
| rs213636600 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108533182 | TGCTTGAAGCTATAA[A/C]CCCCCCCACTCCCCG | 68519 |
| rs213637271 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108526571 | GGGCTTACCAGGCAT[A/G]CCCATTGACGTACTT | 68519 |
| rs213659790 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108444415 | GTTCTCATGGGGCGC[A/G]TACCTCCCATGACTG | 68519 |
| rs213662090 | snp | C/T | | | intron-variant, downstream-variant-500B | Eml1, Gm33385 | GRCm38.p3 | 12:108400266 | TCGTGACCCACAGTG[C/T]CTCAATAGGAATAGA | 68519 |
| rs213667421 | in-del | -/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381248 | AAGAAGTACATTCCA[-/G]ATCTGTGAACCCCAA | 68519 |
| rs213686090 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376056 | CCTGATGTCCCTCTG[C/T]CTAGTCAGGTAACTG | 68519 |
| rs213691199 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108470565 | GTGGATTTGAGGAAT[C/G]GAACCCAAGTCCTCC | 68519 |
| rs213696653 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108382798 | CCTTTTGGGATTCAA[A/T]GCTGAGGTAGAACAC | 68519 |
| rs213716758 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108521591 | ATGAGACGGTCCTTC[A/G]GGGGTGCCGTTGTGA | 68519 |
| rs213718230 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108424139 | ACCCTTGAACAACTG[A/G]AGAAAAATTACATTG | 68519 |
| rs213723500 | in-del | -/CA | | | intron-variant | Eml1 | Mm_Celera | 12:108429148 | GTGTGTGCGCGCGCG[-/CA]TGCGTGCGCGCATAT | 68519 |
| rs213727038 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433579 | CATCCCTGTTGGGAC[A/G]GCTAAGCAATAGCAC | 68519 |
| rs213729951 | in-del | -/CTTGATCTA | | | intron-variant | Eml1 | Mm_Celera | 12:108448905 | AGAGCCAAGGATGGC[-/CTTGATCTA]CTGATTCTCCACTTG | 68519 |
| rs213730667 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108469962 | TTTGCCACCTGAAGA[C/T]CTTTAGTGAGGTGTC | 68519 |
| rs213732560 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108477842 | GGGGACAGAGCGGAC[C/T]GGGGCTCTGAGGGAA | 68519 |
| rs213747366 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478405 | TTATTTAAGATTTTT[A/T]AAAAGATTTATTTAT | 68519 |
| rs213748702 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108529330 | TTGTCCCCTCCCGTC[C/T]CCCCCTCCCCCCAAC | 68519 |
| rs213753185 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520945 | CACACATGCACATGC[A/T]CTTGAGTGTGCACAC | 68519 |
| rs213768530 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108481901 | TCTTTGTATTCAGAT[C/T]CAATAAGTGGAGGTG | 68519 |
| rs213768823 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455559 | AGGTGGCCACCTCCT[G/T]TGTGGACAGCGTCAA | 68519 |
| rs213800310 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390632 | CCTCTAGCTCTGCCA[C/T]TGTGGGCAGTGACTG | 68519 |
| rs213813666 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108477136 | AATCTCAGCACTCAG[A/G]AGGCAGAGGCAGGTA | 68519 |
| rs213834966 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108528694 | CAAGGGATGTGGGCC[A/G]AGACCCCTGCTGGAT | 68519 |
| rs213853166 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108514097 | GGTCCTTCATAGGGA[C/T]CCCAGTCACTAGAAA | 68519 |
| rs213857157 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432844 | TGGAGTGCCCTTTCT[C/G]AGTGACAGAAGCCTG | 68519 |
| rs213861859 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462080 | CTTACAATTGCCACC[C/T]CTTTTCGCTGTGACA | 68519 |
| rs213886856 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108512955 | GTGCAGTCTTCCTGC[A/G]AATCACTTTTTCTTG | 68519 |
| rs213933416 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108519635 | ACAAGCCCTTACTAC[C/T]GCATCCGGATTTTTT | 68519 |
| rs213934896 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108401595 | CTTGGGCCCAAGATT[A/G]GGTATGCCTCCTCAC | 68519 |
| rs213936285 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393647 | TATGCTGCCAGGAAC[A/G]ACACCCCCGATGCCA | 68519 |
| rs213937093 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449782 | CAACGTGCAGCAGTT[A/G]GCTTTCGGCTCACCA | 68519 |
| rs213950101 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443477 | GTGGCCTGAGGAGCC[A/T]GAGTGATTCTTCCCA | 68519 |
| rs213962160 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108453140 | GTTGTGTTTGTGTAT[-/C]TCTGTGTGTTTGTGT | 68519 |
| rs213968558 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108499894 | GTGCTTACAAGGGCT[C/G]TAGCAGTTAGAGAAG | 68519 |
| rs214023704 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484684 | CCCTCAGGAGCTTCC[A/G]AGTCTGCGCTGGGTA | 68519 |
| rs214037533 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108499210 | AGATTTCATAGCCTA[G/T]ACTCACTCACACACC | 68519 |
| rs214043418 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535143 | GCGGGACCCACCCTG[A/G]GGAAGAAGCAGGTGA | 68519 |
| rs214051695 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473889 | CATCATTCCAGGTTG[C/T]AGCCCATCACTTTGG | 68519 |
| rs214056481 | in-del | -/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402802 | GGTTATTCTAGTCTA[-/C]CTTCCTCCACCAGTC | 68519 |
| rs214081307 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108525736 | CAGGCAGATTTCTGA[A/G]TTCGAGGCTAGCCTG | 68519 |
| rs214087653 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480945 | AAATCCCCTTTGGAA[A/G]CAGTCCAGCCCCAGC | 68519 |
| rs214089580 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473445 | ACTGAGGATTTGGAT[A/G]TGGGGACTGCACCTG | 68519 |
| rs214094057 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108477048 | CAACATGGCACCACC[C/T]ATGGTAAGCCTGGCC | 68519 |
| rs214115086 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525014 | TTTGCTATTTTGAAA[A/T]TTTTAAAATATACTT | 68519 |
| rs214117348 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108531872 | GTGTCAGTTACTATG[A/G]TGTCATTAGTACAGT | 68519 |
| rs214122296 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437263 | TGGGTAACTTAAGGG[A/G]GTCTCGATAAAGACA | 68519 |
| rs214161076 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108482515 | TATTATATGTAAGTA[C/T]ACTGTAGCTGTCTTC | 68519 |
| rs214161393 | in-del | -/AT | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404639 | CACATGCACGTGCAA[-/AT]ACACACACATGCACG | 68519 |
| rs214172982 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108480260 | TGCATTTAAGCATGC[C/T]CTCTCTTGCTCTGTA | 68519 |
| rs214175865 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108483660 | GCATGACAAATGTCC[C/T]GAAAGAGCCATGATG | 68519 |
| rs214185903 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108484049 | GAACATGTCAGCGCC[-/A]AAGATGAGAGAAGCT | 68519 |
| rs214193151 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108533893 | AGTCTCCAGGCTCCG[A/C]GTTCTTCCTGTCTTA | 68519 |
| rs214202081 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442820 | GAAACTTCTCTACTC[A/G]TACTTCTCCTGTGTA | 68519 |
| rs214219000 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108491312 | TGTCACTCCCCCCCC[C/T]GCCCCCCAGTGCAAA | 68519 |
| rs214244191 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408327 | CTCACACACGTGCAC[A/G]CATGTTCATGCAATG | 68519 |
| rs214246762 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108396710 | GAGGAAGAGATCAGC[C/T]AGTGCCTGTGTTAGG | 68519 |
| rs214266169 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446814 | AAGGCATGGCATCCC[A/G]TTCCAAGTATGCCAG | 68519 |
| rs214284950 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108396913 | TTCTGATGACTCTCT[A/G]TTGGAGCCTAGTCCT | 68519 |
| rs214306580 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453237 | TGTTTATGTGTGTGT[A/G]TCTGTGTGTATGTGT | 68519 |
| rs214322286 | in-del | -/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406398 | ATTGCCAATATTAAA[-/T]GTTAAAAACCTTTCA | 68519 |
| rs214323522 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108381239 | GTGAGGCTGAAGAAG[C/T]ACATTCCAGATCTGT | 68519 |
| rs214334995 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108411937 | GGAGGGGGAGTTGGG[-/T]TTTTTTTTTTTTTTT | 68519 |
| rs214337533 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108471159 | AATGCTGTGAGAGCT[-/C]GACACAGAGGTGCAT | 68519 |
| rs214337693 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108502532 | GTACTCAGACAACAA[A/T]CAGTCAGTCATTGGG | 68519 |
| rs214351499 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432444 | TAGCTCTGAAAGGTC[A/G]CTGTCAGTGGTGCAG | 68519 |
| rs214355495 | snp | C/G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379297 | GTGTGTGTGGCCACC[C/G/T]GTGCTTGAGCTCATG | 68519 |
| rs214358432 | in-del | -/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473208 | ACATACCACACCACA[-/C]CACACACACACACCT | 68519 |
| rs214363667 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108444676 | CAGAATGTGGGTGCC[-/T]TGACTGAGGACATTC | 68519 |
| rs214393523 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108452220 | TTGTCCATGAGTTCT[A/G]CCTTCATGATTCCCC | 68519 |
| rs214396169 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387584 | AATATGCCACTCCCG[C/T]CTCTGTTTCCCCTCT | 68519 |
| rs214411906 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384437 | GGACTGGAATGATGT[G/T]GCCTGCCACCCCTCC | 68519 |
| rs214419492 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108502090 | GCCACACAAAAGCCA[G/T]GTGGGCACCGTAGCG | 68519 |
| rs214426408 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532676 | CAAAGTGAGTTCCAG[G/T]ACAGCCAGGGCTACA | 68519 |
| rs214432548 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438552 | AAATCTTCTCACATA[G/T]CTTTTAGAACCCAGC | 68519 |
| rs214449378 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484242 | TGGGTGACTAAGGGG[A/G]CTTCCCGCAGGAAGG | 68519 |
| rs214467614 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108534397 | CATACATAAAAATCA[A/G]TAAATCTAAAAGTTA | 68519 |
| rs214478965 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108390168 | GCTTGGAGATGTGAA[C/G]TATGATCCTAGCACT | 68519 |
| rs214494644 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108399726 | GTTTACAGACAGGCA[C/T]CCAGCTCAGAGAGGG | 68519 |
| rs214500998 | in-del | -/CTG | | | intron-variant | Eml1 | Mm_Celera | 12:108441229 | TGTTTTGGAAACAAT[-/CTG]CTTCTTGGGCTGTCT | 68519 |
| rs214518791 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429947 | AACGGCTCCAAGCCT[C/T]GCGCGTTCTGAAGGC | 68519 |
| rs214532112 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108441500 | GGGCTTCACGGAGAC[A/G]AAGCCATTGATGACT | 68519 |
| rs214534230 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108487111 | GCACACAGTGTGCAT[C/T]GACACACTACACATG | 68519 |
| rs214537488 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496894 | TCAGTGATACATTGT[A/G]ACTTCAGAGTTGTAA | 68519 |
| rs214552137 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108492219 | CCTCTGTACAGCCCT[C/G]TTGCTTCGCAGCCTG | 68519 |
| rs214569261 | snp | A/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108537504 | TTTCTTACAGGGCAC[A/G]GACCGACGGTCTGAC | 68519 |
| rs214582294 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447599 | TATGTGTAGAGGGAG[A/G]GGTGATCCCTTGGAG | 68519 |
| rs214618872 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108453960 | AGAGGATGTGTGGTT[A/G]AATGGCTGGATCGCT | 68519 |
| rs214620902 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404876 | CACACACACATGCAC[A/G]TGCAAATACACACAC | 68519 |
| rs214621929 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108496246 | ACCCTAGAATTTAGA[C/T]CGGAAGGCCAAACAG | 68519 |
| rs214644087 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108373952 | CTCCTTGGGTGCAAG[C/T]GATTCTTGGATGCAC | 68519 |
| rs214649364 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108503601 | GTTGTACTGGTTGTA[A/G]ACGTAGGCTGTCCCC | 68519 |
| rs214663758 | in-del | -/CC | | | intron-variant | Eml1 | Mm_Celera | 12:108491303 | CAGTGTGGTGTCACT[-/CC]CCCCCCCCCGCCCCC | 68519 |
| rs214671734 | snp | A/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108420970 | GGGGAGCAGGGGAAA[A/T]GAAGAGGGCTCAGAG | 68519 |
| rs214693224 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407622 | CAGAAGCCTGGAGAG[A/G]GTCCTAGAACCCCTG | 68519 |
| rs214706545 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108373210 | GCCTGTAAAAACAGT[C/T]TCAACATTCATGAGG | 68519 |
| rs214709311 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108384710 | AGATAGTTGTCAGGA[A/G]AGTGTCTATGGTGCA | 68519 |
| rs214718177 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108465369 | CATCAGAGGCACACA[C/T]TACCCTCAGCTCTGT | 68519 |
| rs214733125 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108420086 | TTATAATGCTATGTA[A/G]ATTATACCTAATTGA | 68519 |
| rs214741671 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108517071 | AGGTCTTCCCCTCCA[A/G]CTCCCAGTGATGAGC | 68519 |
| rs214755151 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108435867 | GTGTGTGGAAGCTTC[C/T]GTTACCACTTCCAAC | 68519 |
| rs214759555 | in-del | -/TGTGTGTGTGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108467803 | GCACGTGGATAGAGA[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 68519 |
| rs214770797 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108372639 | CCAGGATCGTGGTAC[A/G]GCACTGAGTGTGCAT | 68519 |
| rs214771025 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379348 | TGAGTCCATTTTTCT[C/T]CATTCACATTTACAA | 68519 |
| rs214790857 | in-del | -/ATTTATTTATTTA | | | intron-variant | Eml1 | Mm_Celera | 12:108379680 | CTTTATTATTTATTT[-/ATTTATTTATTTA]TTTTTTTTTGTGACA | 68519 |
| rs214796723 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429359 | TTCTGATGTCGGTAA[G/T]ACCGGTGGCTGTCTC | 68519 |
| rs214827561 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442392 | AGACAACTCAGCGCA[C/T]ACCAGTCTTTCTGCT | 68519 |
| rs214870481 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108489081 | CATGTTGGGTCGGTG[A/C]GGTTCCCGTGCTTTT | 68519 |
| rs214872100 | in-del | -/ACAATGTTTTC | | | intron-variant | Eml1 | Mm_Celera | 12:108534528 | AAGATACATTGAAAA[-/ACAATGTTTTC]CCAATGTTTTCCTTT | 68519 |
| rs214886488 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450895 | CACATGAGGTTGAGG[A/T]TTTTAGGAAGATCAT | 68519 |
| rs214903209 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108458953 | CTCTCAGCTACTGCA[-/C]CAGCGCTATGCCTGA | 68519 |
| rs214929234 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108389613 | GGTGCCTGGAACCCA[A/G]TGCCACCAATATGGA | 68519 |
| rs214946119 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409389 | TGAGCTGCTACGGAA[C/T]GGTCTTAGGCTGTCT | 68519 |
| rs214946757 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108420139 | TATTCTAAATTTTGC[-/TT]TTTTTTTTTACCCAA | 68519 |
| rs214972892 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108440953 | TGTTGCTGAACTTTT[C/T]CAGGGGTTCAGTCAC | 68519 |
| rs214978220 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457215 | AGGAACGCTCCTGTC[G/T]GAAATAAGCTTTGAC | 68519 |
| rs214979122 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450148 | GCACCGGGGTCACCG[C/T]CTCGTGCTACCTACT | 68519 |
| rs215001043 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408564 | CCCTCCCCCAGCAGC[C/T]ATAGTTAAATGCCCA | 68519 |
| rs215008853 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108486417 | CTGCACCAGTGGCAG[C/T]CTGGTGCCTTCTCTC | 68519 |
| rs215016361 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456579 | CACTTTGCCACCATA[C/T]CCCTCTCTCTTGAAC | 68519 |
| rs215055855 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108506264 | TTGTGGGATGGAAGC[A/C]AAAAACCAACTCCCA | 68519 |
| rs215106797 | in-del | -/AAA | | | intron-variant | Eml1 | Mm_Celera | 12:108492545 | AGTTACCTGTTTCTG[-/AAA]AAAAAAATCCCAAGA | 68519 |
| rs215109750 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108508213 | GGATCCACTTGATGG[A/G]AGGAGAGGGCCAACT | 68519 |
| rs215112427 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108462749 | AAGATTCTAAAAACG[A/G]GGTGGTAGAGACAAG | 68519 |
| rs215122979 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108464671 | AAGAACAAGAACAAA[C/T]CTTTCTTGAACCATG | 68519 |
| rs215138487 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108514006 | TCGTTGATGCAGAAG[C/T]AGAAGCAAGAGAAGT | 68519 |
| rs215162521 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108375518 | GAGTTGGAGTTTAGC[C/T]CCTGGTCTCCCACAA | 68519 |
| rs215166901 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108466040 | TTCCCTGCTATGGCC[G/T]GCGATACCTGGAACT | 68519 |
| rs215180103 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433203 | CGTGAATGAGGGACC[A/G]TGAGTGGTGGGTCTG | 68519 |
| rs215188612 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108517732 | CCTCAAACTCACAGC[A/G]ATATTCTTCTTCAGT | 68519 |
| rs215192728 | in-del | -/GA | | | intron-variant | Eml1 | Mm_Celera | 12:108372972 | ACAGAAAGCAAAATG[-/GA]GAAAGAGAGAGAGAG | 68519 |
| rs215249575 | in-del | -/TG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451333 | ATATGCAGATATACA[-/TG]CACGCACACACACAC | 68519 |
| rs215291398 | in-del | -/GCTC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507276 | TCTGTGCTAACTCCA[-/GCTC]GTGTCAAGTTGCCAC | 68519 |
| rs215291694 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378104 | GGTTCATTTATTGTA[-/T]TTTTTTTAAAAGAAT | 68519 |
| rs215302252 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458328 | GCAGGACTCTGGGTC[C/T]GGACTGACCCATGTT | 68519 |
| rs215343332 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405466 | ACTGTAGGGAAGAAC[G/T]TGGGCTAGCTCCGGC | 68519 |
| rs215343710 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449102 | ATTGGTTTCGTTTTT[-/G]TTGTTGTTGTTGTTT | 68519 |
| rs215357297 | in-del | -/TGTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108502363 | TAAATAAATAAATAC[-/TGTTT]TTTTTTTTTTTGGTT | 68519 |
| rs215374845 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508163 | GTGGCTAAAGGTACC[-/T]GCTAACAAGCCTGAA | 68519 |
| rs215406341 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108382411 | GTGAACTTCCGGTTG[G/T]ATGAGTGACCCAAGC | 68519 |
| rs215445290 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108416761 | ACCATGGGCCTACAT[C/T]CACCCCTTGGCTATA | 68519 |
| rs215447478 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108478304 | AGTGTGTGGGGTTTT[A/G]AATGTTCTGTGGCTT | 68519 |
| rs215464996 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108510660 | ATCAACACGAAAATA[C/T]ACCAATCTAAGCAGC | 68519 |
| rs215465517 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381965 | GAGTCGGGGTCCATG[A/G]TGAACATCTTCACCA | 68519 |
| rs215470491 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108463071 | TCAGACCGACCTGCT[G/T]TGGTTTCAAGAGGCT | 68519 |
| rs215481798 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530092 | TCCCATGCACATACA[A/T]GTCCCAGAGAAAACC | 68519 |
| rs215497156 | in-del | -/C | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421726 | CACACCCAACCTCAG[-/C]CCTCTAACCCACCCA | 68519 |
| rs215504927 | in-del | -/CC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473312 | CATACACCAAGCATA[-/CC]CACCCCCCCCCAAGC | 68519 |
| rs215527359 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108477957 | GAAAGCTTAGGGTAT[A/T]TATTGTGTAGAAGGG | 68519 |
| rs215528693 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108485203 | AGGAGCCCAGCGGGG[A/G]CTGCGTGTAGTGGGG | 68519 |
| rs215551884 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108484861 | TGTCCCTAAATTGAG[C/T]ATTCTAAAACAAAGA | 68519 |
| rs215552386 | in-del | -/GGGTGGGGGT | | | intron-variant | Eml1 | Mm_Celera | 12:108374347 | TAGAGAGCATGTGGG[-/GGGTGGGGGT]GGGGGACTCTGTTTG | 68519 |
| rs215595950 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108511662 | CCTAGAGTTTCCTTA[A/G]GTCACTGCGAATGTT | 68519 |
| rs215602167 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108413782 | CTCTGGGAGAACAGC[C/T]AGTACTCTTAACTGC | 68519 |
| rs215631593 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475190 | TGCTTTGACTCTCTA[G/T]ATGTAACACCAACAA | 68519 |
| rs215656006 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108461203 | TCCTAGCACACAGTG[A/G]GCCACTCACCATTCA | 68519 |
| rs215666619 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108510888 | TAGGAGACGTCCAAG[C/G]TGGCATCCACGAGTG | 68519 |
| rs215689669 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108485684 | ACACACACACATACA[-/TG]CACACACACATACAC | 68519 |
| rs215691512 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419300 | TTGTTTATCCAGTCC[A/G]TCACTGGACTTTATG | 68519 |
| rs215693294 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379890 | AGCCCACTATGTAGC[C/T]CAGGCTAGCCTCAAA | 68519 |
| rs215709727 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108531664 | AAACAAACAAACAAA[-/C]AAACAAAAACAAAGA | 68519 |
| rs215749793 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108444697 | GAGGACATTCGTGTG[A/G]CTGTACCTTTGTGAT | 68519 |
| rs215782304 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436566 | ATCTAGGAATCCTGA[A/G]TCTTCTGGGTTAAGC | 68519 |
| rs215787080 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492786 | AACAATGCTAAGGCA[C/T]GCAGTAGGTGCCCAG | 68519 |
| rs215791328 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108371609 | TGGGCTGTCAGCCTG[A/G]AGAAGGGGCAGGGCT | 68519 |
| rs215796878 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108481839 | TGGCCAGACAAGGCA[A/G]CCCAGTTAGGAGAAC | 68519 |
| rs215811630 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418067 | GATGACTGTGTGTCT[A/G]TTTGATAGGACTTCT | 68519 |
| rs215829095 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108500611 | GAGCTTGTACTGCAC[A/G]GGTGCTCGCTGTGCC | 68519 |
| rs215829653 | in-del | -/A | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499229 | CACTCACACACCCCC[-/A]CCCACACACACACAT | 68519 |
| rs215841732 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532577 | AAATATAACTGGGCT[A/G]GGCATTGGTGGCGCA | 68519 |
| rs215861207 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108436715 | TTCAGATCCAGTAGC[G/T]TACATTCTCTCTGCA | 68519 |
| rs215865631 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108464334 | TAACTTTGTAGTGAT[C/G]GAGCCTTCACATTTC | 68519 |
| rs215874704 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488998 | GTTATGATAAATATG[C/T]GAAATGCACTCTAAC | 68519 |
| rs215903842 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442017 | TGGCTTGATACTTGG[A/G]TGACATTTTCATAAA | 68519 |
| rs215912238 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108488102 | TGTGTCACTTGCTCA[G/T]TCACAAAGTGTGCAG | 68519 |
| rs215945136 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524228 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 68519 |
| rs215945943 | in-del | -/TTT | | | intron-variant | Eml1 | Mm_Celera | 12:108532211 | TTTGGATACAGGGTC[-/TTT]TTTTTTTTTTTTAAG | 68519 |
| rs215968258 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108476950 | GAATGTTGTTTACTG[A/G]CTTGTTCAGCCTGCT | 68519 |
| rs216004865 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108383782 | TTAAAACTTTCTTCC[-/A]AAAAATTATTTGAAT | 68519 |
| rs216005711 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108484087 | GCTCTGTAATCCTAG[C/T]GCTCCTCCCTCTATC | 68519 |
| rs216005857 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476524 | GTAAGACAAAGGCCC[A/T]CCCTCATCCCTTGGC | 68519 |
| rs216021313 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437894 | ATCGCACAGGTTTCT[G/T]CGAAGCAGATGTCCT | 68519 |
| rs216080854 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388854 | GCTATACCATAAGAA[C/T]ACAGGGCTTGCCCAT | 68519 |
| rs216083589 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108483425 | AGGAGCTTCCTGCAG[C/T]GAGTTGACAACCAGC | 68519 |
| rs216097616 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108533712 | CATGGACAGGGATGG[A/C]TGGTCAGCAAGAGCC | 68519 |
| rs216106780 | in-del | -/CACACACACACACACA | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409873 | TCTGTGTCTCTCTGT[-/CACACACACACACACA]CACACACACACACAC | 68519 |
| rs216117752 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108469823 | GCTCCCGCTGGCTTG[C/T]GATTGCTGTTTCATC | 68519 |
| rs216144641 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108395486 | GGCACACAGCTGCCC[G/T]GCCAGCCTAGCCAGT | 68519 |
| rs216155253 | in-del | -/TTTGTTTTTGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108439255 | GTTTTTGTTTTTGTT[-/TTTGTTTTTGTG]TAGAGCTGACTGTGC | 68519 |
| rs216155713 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108520930 | TGTGCATACACAATA[C/T]ACACATGCACATGCT | 68519 |
| rs216172367 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108435099 | CTTGGTAACAGAAAA[C/T]CAGTGAAGACAACTG | 68519 |
| rs216183443 | in-del | -/ACACACACAC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108526247 | AATGCATCGTACAAT[-/ACACACACAC]ACACACACACACACA | 68519 |
| rs216190363 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm33385 | Mm_Celera | 12:108400460 | CGGAAGGGGGAGGGT[A/G]AACCACACACAGCAT | 68519 |
| rs216190527 | snp | C/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407329 | GTTGCTTTTCCTGCA[C/G]AGAGGGGAGAAAAGA | 68519 |
| rs216202545 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445383 | ACTTTTCCATAGCCC[C/T]GTGAGCTCCAGCATC | 68519 |
| rs216204750 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108493367 | ACCATCTGTACTTCC[A/G]GTTCCAGAAGATTCA | 68519 |
| rs216209380 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455520 | AGTTGCTCTTCCGAT[A/G]TTTGTGCCAGTCCCT | 68519 |
| rs216216932 | in-del | -/TGGAAAAACACAGATAC | | | intron-variant | Eml1 | Mm_Celera | 12:108528115 | GACCCCCAAAGACCA[-/TGGAAAAACACAGATAC]TTATATTATGGTTCA | 68519 |
| rs216218391 | in-del | -/GAG | | | intron-variant | Eml1 | Mm_Celera | 12:108383517 | TTACTTACAGTTTAT[-/GAG]GAGTAGTCACATTCT | 68519 |
| rs216258899 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406239 | ATTTGTCTCTCTACC[A/G]GTTCTCTGACTTTTT | 68519 |
| rs216266427 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410720 | CCCCTCCCAACCCCA[C/T]TCCGGGAGCAGTTCT | 68519 |
| rs216297393 | snp | C/T | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108370391 | TCACAACTGGAATGA[C/T]CCCTGGTCCCAGGGG | 68519 |
| rs216328896 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108383959 | CTATATCAGCTGCAA[A/G]AAGCAATCCTGAGAT | 68519 |
| rs216333885 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108480169 | GAGAGAAGGAAGGGG[A/C]TGTGGGCTTATAGAC | 68519 |
| rs216349358 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417569 | AAGCTTCAGGCATGT[C/T]GCAGGCAGACAGAAT | 68519 |
| rs216356778 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108463773 | CAAAATGCCCCGAGC[C/T]CCACCCACTGAACCA | 68519 |
| rs216358419 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421196 | ACTTCCCAACTACAT[C/T]GTCTCTCCACAATGC | 68519 |
| rs216361914 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108434304 | TGTAGTCAGGAAGGG[A/G]GATGAGGAGGCAGCT | 68519 |
| rs216363406 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108441428 | AACATCCTGCGGGGA[A/G]TGGCTTGCCTGTTTT | 68519 |
| rs216363789 | in-del | -/CACACACA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451338 | GCAGATATACACACG[-/CACACACA]CACACACACACACAC | 68519 |
| rs216371684 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486965 | GAGGGGATCTTGAGT[A/G]AAAAGAGTAAAAGAT | 68519 |
| rs216384013 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108515627 | AGATGCGCACAGGGC[A/C]GCTCAGAGGCTGACG | 68519 |
| rs216387447 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108467014 | CCAAACTCAGGTCCC[G/T]TGAAAGATTCGTGCA | 68519 |
| rs216390129 | snp | A/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413633 | GTGTATGGTTATTTT[A/G]TCTGCCTGTGTGTCT | 68519 |
| rs216391110 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108389585 | GATTTAGGGTTTGGT[A/G]TATGAGGTATGGGGT | 68519 |
| rs216414204 | snp | G/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108537265 | GAAGGTGGATTTCTG[G/T]CCCCTTTGGTGACCA | 68519 |
| rs216420132 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440907 | ACGGCCTGCTCCCGT[C/T]ACTTCACTGCCACGT | 68519 |
| rs216457083 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486335 | CATGGTCTGTTGACT[A/G]ACAAGCCACAGAAGA | 68519 |
| rs216464469 | in-del | -/ATATATATAT | | | intron-variant | Eml1 | Mm_Celera | 12:108467949 | AATAAAACTGATAGA[-/ATATATATAT]ATATATATAGTTTAT | 68519 |
| rs216467490 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108471175 | GACACAGAGGTGCAT[A/C]TCCATAATGTAAGTG | 68519 |
| rs216490445 | snp | C/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536674 | GAGGCACAGGACAGC[C/G]CCCCCTAGTGGTTAT | 68519 |
| rs216497555 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474585 | GGGGACTATGCTGTG[A/G]TTTGGTTTGTGAAGT | 68519 |
| rs216501361 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108522354 | TAGTGCTAATAATCA[G/T]GTGGCAGGAGGCAAG | 68519 |
| rs216510050 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108416136 | CGGAAAACTGGAAAG[-/AG]AGAGAGAGGGTCGTC | 68519 |
| rs216522613 | in-del | -/ACCT | | | intron-variant | Eml1 | Mm_Celera | 12:108496822 | CAGCACCTCTCCAGG[-/ACCT]TGCTGCATCATCTCC | 68519 |
| rs216532791 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108526392 | GTGGCAGAGTTACTT[A/G]TAAAGGTCACGGAGT | 68519 |
| rs216574123 | snp | C/T | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411223 | GCTGTCTGTATTCCT[C/T]ACCAGGTGTTCTTAG | 68519 |
| rs216613617 | in-del | -/CT | | | intron-variant | Eml1 | Mm_Celera | 12:108429180 | CATGAGTGTTTGTGC[-/CT]CTGCCTTGCATGTGG | 68519 |
| rs216618531 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108388245 | CTTGTGGCTCTACCC[A/C]TCTGTGGTGAGGACA | 68519 |
| rs216625613 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508193 | AGCCCTGCGTTCAGT[C/T]TCCAGGATCCACTTG | 68519 |
| rs216672475 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108439522 | TATGGATGGCTGAGT[A/G]CCACCATGTGGTTGC | 68519 |
| rs216727622 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108387409 | GGCGCCACTTTGGGA[A/G]GTTATGGGTCCTATG | 68519 |
| rs216734492 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469143 | CCCCTCCCCCTCCTC[C/T]CGGCCCCTCCCCTCC | 68519 |
| rs216738464 | snp | A/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404821 | ACGTGCAAGTGCAAA[A/T]ACACACACATGCACA | 68519 |
| rs216744865 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374660 | AATTCAGAGGCTTTG[C/T]CCCAAGCCTAGGGCC | 68519 |
| rs216775519 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461458 | TGCACAAACATCATG[A/G]CCAAGAAGCAAGTTG | 68519 |
| rs216782443 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519950 | CCCAAGCTTCATCCT[C/T]GCTTTTTGTGATGTA | 68519 |
| rs216825478 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108460147 | CATCGCCAGTGTCTC[C/T]AAAGATCAGGCTTTG | 68519 |
| rs216830983 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467674 | TTCCTCTGGCTCTGC[A/T]AAGTGCTTCCTGCCT | 68519 |
| rs216844670 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433326 | GTTAGCAGTCTTAGC[A/G]CGTTATTTCCTGCCA | 68519 |
| rs216872300 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108509939 | GGTGGCGACTAAGTC[A/G]GTGGTTCTGAGAAGG | 68519 |
| rs216874089 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519081 | AAGTCCTTGATCACA[C/T]GCATGCCATCCCATG | 68519 |
| rs216904361 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517670 | AACTTTTTTTTCTTA[C/T]TATATAGTCCAGGAT | 68519 |
| rs216905688 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108509002 | ACTGATAGCACCATT[G/T]CACAGCATCTTTGGG | 68519 |
| rs216970752 | in-del | -/AACTCTTTA | | | intron-variant | Eml1 | Mm_Celera | 12:108484571 | AAGAGTGTTTTATGC[-/AACTCTTTA]AACTGCTATGAACTT | 68519 |
| rs216985362 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108516998 | ATTTCACCACCTGAG[A/G]CCTAGACAGCAGCCT | 68519 |
| rs217001678 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393163 | CATTGTTACATCTCA[A/G]ATCCTACAGGTAGTG | 68519 |
| rs217017476 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108504780 | GCCTCAGATCGACAT[-/A]TTTTTTTACTTTGGC | 68519 |
| rs217021218 | in-del | -/CACACACAC | | | intron-variant | Eml1 | Mm_Celera | 12:108390047 | CCTTAAAAAAAAAAA[-/CACACACAC]ACACACACACACATT | 68519 |
| rs217025598 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392136 | GCATGAACAAGCTTG[C/T]TGCTGTCCAGGCACC | 68519 |
| rs217061613 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442348 | TGTGCATGGCCTCCC[C/T]GCCACTCAGCACCCA | 68519 |
| rs217075933 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442906 | ATCAGTAAACCCTGA[A/G]GAATGTTACCAAGGT | 68519 |
| rs217121762 | in-del | -/CCC | | | intron-variant | Eml1 | Mm_Celera | 12:108487891 | TCTACCCAGTAGCAA[-/CCC]CCCCCCCCCATTTGT | 68519 |
| rs217121819 | in-del | -/GC | | | intron-variant | Eml1 | Mm_Celera | 12:108433500 | ATTGGATGGAGTTGG[-/GC]GCTCTCTCTCTCTCT | 68519 |
| rs217125453 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108490669 | AGGTGGCTGCCTCCC[A/G]TCTGAGAAGATGTGC | 68519 |
| rs217126325 | in-del | -/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403701 | AACTCAATTGATAAC[-/T]TTAAAAAAAAAACCA | 68519 |
| rs217140506 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108390867 | cacacactacataca[C/T]acatatcacatacag | 68519 |
| rs217145098 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407791 | ACTTCAGACTCTGAC[A/G]TCTATGGTGGCTTGG | 68519 |
| rs217145155 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416150 | GAGAGAGAGAGGGTC[A/G]TCATCCCCCTCCCCC | 68519 |
| rs217169286 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447886 | CAGGTGCCCTGCGGG[C/T]CAGGTGAGAAGCAGA | 68519 |
| rs217173818 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108496742 | TGGGGCCACCTCTGG[A/C]CTGGTGATCCTGGGT | 68519 |
| rs217182029 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108415386 | AAAAAAAAAAAAAAA[A/G]AAGAAGACCTACTTT | 68519 |
| rs217187010 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108497894 | TCAGGAAGGTCGAGA[A/G]CCACTGGATAAACCA | 68519 |
| rs217194940 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108513853 | TTAAGAACATAGAAT[C/T]GAATCATTACATAGA | 68519 |
| rs217219683 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108513268 | TTTAATTAATTTTAG[A/T]CAACCAGTCACTTCT | 68519 |
| rs217221020 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108520857 | GGTGAATCCTTGCCT[A/G]GATTGGAGAGGTCCT | 68519 |
| rs217253780 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108471659 | AATATCTGTGTAGGG[C/T]GAGGATGCTATCTAG | 68519 |
| rs217273228 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108462145 | ACTATTTTTATCTTT[A/G]TATCTAAAGTGTGTC | 68519 |
| rs217273276 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108469447 | TCTGTTAAGTTCACA[A/G]TTAATGCTAGCAATC | 68519 |
| rs217283532 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519837 | TTAAAGGCGTGCTCT[A/G]CCACCACCCAGCCAC | 68519 |
| rs217287510 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108386943 | TGAAGGGACTTAATC[A/G]GCCTGTCACAGTGGA | 68519 |
| rs217306071 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469082 | TGTGGTCCCCAGAGC[G/T]CCAGAACATTGTGGA | 68519 |
| rs217320680 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108438913 | CAGGAGCTGTCAGAC[-/TG]AGAGGAAAGGAGGGA | 68519 |
| rs217354648 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393593 | AAGGAACCTGTGAGC[A/G]TGTGTGGGTCCTAGA | 68519 |
| rs217379606 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108463223 | CTTGATGTAAGCAGA[A/G]TCTGATATCACTTGG | 68519 |
| rs217406803 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108491174 | TCGACCGCAGGAGGC[A/G]CGAGTTCTGGCTGGA | 68519 |
| rs217479244 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416850 | CATCAATAAGGACAC[A/G]GTATCCTGGGTGCTA | 68519 |
| rs217504481 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108498775 | GAGATGGCTTGGCCC[A/G]GCCCGTCATGTGGGT | 68519 |
| rs217510044 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108382357 | GGTAGAGACAAGAGG[A/G]TCATGGGAGCTGGCA | 68519 |
| rs217542189 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108444547 | CCAGAACTGTTCATC[A/G]CCATGGATACGATGG | 68519 |
| rs217556893 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108514857 | GCATAGCCCCTCCCT[C/T]ATGTCCCCCTTACCA | 68519 |
| rs217559048 | in-del | -/TACC | | | intron-variant | Eml1 | Mm_Celera | 12:108494034 | GGCATCACTCTGAGA[-/TACC]TGTCACCCAGCTGTG | 68519 |
| rs217559649 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108514030 | AGAAGTGGGGGACCT[-/G]GGCAGCCACAGTAAG | 68519 |
| rs217580364 | in-del | -/TT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108483567 | AAAGGAAATGTTTTA[-/TT]TTTTTTTTTTCTTCT | 68519 |
| rs217594494 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443908 | GCGTGTTTCAAGATG[C/G]TAACACTTTGAGTGT | 68519 |
| rs217597538 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108521612 | GCCGTTGTGATGGTG[A/G]GATCTCAGAGTCCCT | 68519 |
| rs217612050 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108424584 | AGAGGCATGAAGCTC[-/A]AAAAAAAGGAATGAT | 68519 |
| rs217615464 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108472008 | ACTTGAAGAACCCCC[-/T]CTCCCTCCCTACACA | 68519 |
| rs217646667 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108388193 | AGGTAGAAGTCCTTC[C/T]ACGCATCCTGCAGCT | 68519 |
| rs217658340 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108472119 | GAGGCTTGCAGAAGC[C/G]CAGGCTTTGATGCCT | 68519 |
| rs217700190 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387735 | TGTGTGTTCAAAGAC[C/T]GAGCTGGAGAACTGA | 68519 |
| rs217702773 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372713 | CTCTTCTTTGTCTGG[A/G]GGTGGGGTCAGTACT | 68519 |
| rs217707445 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484752 | ATTTTCATCATGGAG[A/G]ATGGTGACCTCCGGG | 68519 |
| rs217709653 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108524320 | CAAGAAGAATGAAAT[A/C]ATCCCATGCATCCTA | 68519 |
| rs217714504 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479454 | TTTGTTGGTATCGTG[G/T]ATACTGGTCTCTATT | 68519 |
| rs217735351 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403392 | TGCGCCACCACTGCC[C/T]GTCTGCATCTGTCTT | 68519 |
| rs217757013 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372041 | AACAGATGTGGCTAC[A/G]CACCTACCGTGCGGT | 68519 |
| rs217765057 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452110 | CTGTTTCGCTTCTCC[G/T]GCATGCCGTCTTTTA | 68519 |
| rs217766116 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108465654 | GACGAGTGACAAACT[A/G]GAAAGAGATGACTTT | 68519 |
| rs217771780 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108484321 | CAGCCGCTCTTGGAA[A/G]CTCAGGCAAGTTGCT | 68519 |
| rs217795742 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473563 | TGAACCCCAGCCATG[A/C]CATCTGGGTGCAGGC | 68519 |
| rs217798350 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464758 | CCCCACTGCATGAGG[C/T]GGCATGGGTTTACAG | 68519 |
| rs217799634 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108397390 | TCACTGCCACAGCCA[C/T]AGCCACATGTTGCTC | 68519 |
| rs217807071 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492248 | TGTCCAGGACAGCTG[G/T]GCTGGTCTCTCTGGC | 68519 |
| rs217812915 | in-del | -/AGTT | | | intron-variant | Eml1 | Mm_Celera | 12:108515469 | AGGATACAATGATAA[-/AGTT]AATCACTTTGCTGTG | 68519 |
| rs217871611 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108395843 | AAGGCTGAGGCCAGT[A/G]ACCTCAGTCTGAATG | 68519 |
| rs217888294 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108414518 | GCTCACTATACAAGC[A/C]TGAGAACCTGAGTTT | 68519 |
| rs217909994 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108419411 | ATATACATGATGCTG[A/G]CATACATGTGGGTAT | 68519 |
| rs217915770 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445734 | TGCATGAAAATTTTG[G/T]ATGCAGAAAATGATT | 68519 |
| rs217927011 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108371894 | TACCCTGATGTGTGT[-/TG]AGGATTAGCTACCTG | 68519 |
| rs217948311 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108440999 | GTTCACCATCTCCTG[C/G]TTCATGTCTGTGTCT | 68519 |
| rs217972467 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108463434 | TCGTCTTAGGTCGGC[-/AG]AGTGTATCACGTGCA | 68519 |
| rs217978267 | snp | C/T | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370166 | ATTGACCTGAGAGAG[C/T]GGGGACAACCGGAGT | 68519 |
| rs218007273 | in-del | -/GT | | | intron-variant | Eml1 | Mm_Celera | 12:108448128 | TTATTTTATTTTTAA[-/GT]GTGTGTGTGTGTGTG | 68519 |
| rs218020254 | in-del | -/AAT | | | intron-variant | Eml1 | Mm_Celera | 12:108425164 | CATTCAGTTAATTAC[-/AAT]GACAATGATTCGGTT | 68519 |
| rs218023059 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108518834 | GGGATTAAAGGCATT[C/T]ACCACCACTGCTCAG | 68519 |
| rs218024746 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108451570 | TTCAGATGTGCTCAC[A/T]GTAAGCCTGACACTC | 68519 |
| rs218032723 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108501269 | AGCATATGGCTCGTT[C/T]CTGTTGATGAGTGTA | 68519 |
| rs218037030 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108516719 | ATGAATTTTATGGCG[A/G]CAACAATCTTAGAAA | 68519 |
| rs218046068 | in-del | -/TTTGGTTGGTTGG | | | intron-variant | Eml1 | Mm_Celera | 12:108520614 | GGTGGTTGGGTTTTT[-/TTTGGTTGGTTGG]TTGGTTGGTTGGTTT | 68519 |
| rs218071695 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108447439 | CACCAGGGACCAGCA[C/G]AGGACAAGCTCCAGG | 68519 |
| rs218101941 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108392333 | CCTTGTGCTGAGGAC[A/G]AGGGGGTGAGGCAGT | 68519 |
| rs218129834 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526011 | CAAAGTGCTAGAAAG[C/T]CCCGTGAATATCCCG | 68519 |
| rs218151527 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489165 | GAGGAGTCCAGGAAG[A/G]AGCCTCGGCTTCAGA | 68519 |
| rs218155869 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108391374 | GTGAAGGATCGTCTT[G/T]CTTACATTACCTGTG | 68519 |
| rs218163106 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496117 | TTAGGGAGCCAATGC[A/G]AATACTGGGGTGCTC | 68519 |
| rs218168409 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108389370 | CATGAGAAGAAGCAC[A/G]ATTGGCCTCTAAGTC | 68519 |
| rs218176315 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108397186 | GATGCAGTGTAAAGT[C/G]ATGGATTAAGAGTTG | 68519 |
| rs218187329 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486233 | CTTGGTTAAGGTTAA[-/G]GGATTAAGGAAGGTG | 68519 |
| rs218188533 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108488449 | TGTTGCCTGTACCTT[C/G]TTCCATTTATTACCC | 68519 |
| rs218245362 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108459595 | GACAGGCCCTAGTCT[-/C]CTCTTTTAAGATTAA | 68519 |
| rs218306933 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453495 | GTGGTGGGGTTACAG[A/C]CATGTGCTGCCCTCT | 68519 |
| rs218317674 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442443 | TACTGAAAATGAAGA[C/T]TCACGGTCCACACCA | 68519 |
| rs218327670 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108373103 | TCCTGGAATTCATCT[C/G]CAGACATTCAGGCTT | 68519 |
| rs218328043 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108495533 | AAGGGACAGGCCCAC[A/G]CTGCATTTTTGGCAG | 68519 |
| rs218337361 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108521839 | TCTTCTGGGATATAT[C/T]TTTGTATGAATTAAC | 68519 |
| rs218362161 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419970 | TTATCTCAAAGTGAC[A/G]TGGAATAATAGTCTG | 68519 |
| rs218368455 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442157 | CCCACGTGGCATTGC[A/G]TGACCAAACGTGGGG | 68519 |
| rs218373431 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108372404 | TCGCCTGCTTCCACC[A/G]GGCGCCAGCAGAGCC | 68519 |
| rs218392530 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388308 | TCCAGGATCATCTCT[C/T]CCCTGAAGTTCTAAA | 68519 |
| rs218401104 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402648 | GGTAAAATACGTAGC[C/T]GCACTTGTAACTATA | 68519 |
| rs218405527 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419224 | ACCATGCAGCAGCAG[C/G]TGTCAGAAGTCCTTT | 68519 |
| rs218410323 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108529491 | CACCCACAAGTATAC[A/G]TACCATCTTCCATTT | 68519 |
| rs218411532 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108465824 | TCATGGGGAGGGGGC[A/G]GAGCTAGGCATTGGA | 68519 |
| rs218439445 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447655 | AGGCTTCGTGAAGCA[G/T]CGCCTGCAGTGGAAT | 68519 |
| rs218446361 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387938 | TTGGTAGATGTCTGC[C/T]GAATGTTTCTGTGCC | 68519 |
| rs218474431 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447186 | TTTGAGAGAGCCAAG[C/T]GCCTTCTAACACAGG | 68519 |
| rs218483392 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108529065 | AAGTGGAAGGACAGC[A/G]GAGCAGCTCCCTGGC | 68519 |
| rs218494249 | in-del | -/A | | | intron-variant | Eml1 | GRCm38.p3 | 12:108466629 | TGTGTGTGTGTGTGT[-/A]GTGTGTGTGGTGTGT | 68519 |
| rs218513858 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108413390 | GTTGGTAAGGGGGTC[C/T]TGAGAGTGACTCCTG | 68519 |
| rs218540745 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108472773 | AATCAGGGAAGACTC[C/T]TGATTTCAACTACAT | 68519 |
| rs218541997 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384327 | CTCCAGCCATCTGAT[A/G]GAGCAGCTGGGGACT | 68519 |
| rs218571939 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108518706 | TTTGTTTAGTTGGTG[-/T]TTTGTTTGTTTTAAG | 68519 |
| rs218583131 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108428186 | CTGTTTGTGTGGGGC[C/T]GTTGGGGGCCCCATG | 68519 |
| rs218594352 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470415 | TTATTAGATTAATTT[A/T]AAAAATTTTAATGGG | 68519 |
| rs218602923 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108524847 | AGGGAGACATAACAA[C/T]GAAATATATCTTCAA | 68519 |
| rs218606495 | in-del | -/CA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474627 | GGTCATAGTTCAGAT[-/CA]GGAGAGTCATTATAA | 68519 |
| rs218612581 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500202 | AACTTATATCTAACG[A/G]AACAATTCTCATCTA | 68519 |
| rs218620333 | in-del | -/ACACACACACAT | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409692 | CACACACACACACAC[-/ACACACACACAT]ACATACCCAGTCTTT | 68519 |
| rs218640858 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108450038 | TAGGACAAGACGTGT[G/T]TGTGGCGGTTGAACT | 68519 |
| rs218645943 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499632 | TTGTTACCTGGAAGT[A/G]TAACCTGACATTAAC | 68519 |
| rs218666658 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108444854 | ACTAGGGATGTTCTG[A/G]CTTACAGACCATCTG | 68519 |
| rs218691408 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108446254 | CACTGACCATAAGGT[A/C]ATTAATATGTCAGGG | 68519 |
| rs218717154 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500075 | GAAATTACCTCATAG[C/T]CACAGTTACAAATTT | 68519 |
| rs218721899 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108444026 | AATTTTTAATTGGCA[A/G]TTATTATTTATGCAC | 68519 |
| rs218753518 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445846 | AATGGCAGAACTTAC[C/T]AACGATTCCTTCAGG | 68519 |
| rs218755974 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108456499 | TCCCTCTGGCGGGTC[A/G]CTACCACACCAGCCC | 68519 |
| rs218764411 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108506210 | TCAGCAGGTAAAGCC[A/G]CTTACCCAAACCTAA | 68519 |
| rs218783284 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443642 | GCCCTGGGGCATAAA[C/T]GATGAGCACTGCCAC | 68519 |
| rs218797022 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108450261 | CTACACTTCCGGGGG[G/T]TGGGGGGGTTTATCT | 68519 |
| rs218848776 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455649 | GCTGAGCATGGTGCA[G/T]CAGGAGGGCTGGAAG | 68519 |
| rs218858214 | in-del | -/TTCC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108420441 | ATTTTTTCTTTCTTT[-/TTCC]TTCCTTCCTTCCTTC | 68519 |
| rs218906915 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108423740 | ATGTGCTCCAGAGCC[C/T]GGGTGGACCTGGCTT | 68519 |
| rs218909087 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417730 | TGGAACAGACAGTTG[C/T]ATTGTCAGGCAGGCA | 68519 |
| rs218926731 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108494078 | GCTTCAGAGTCTAGA[-/G]GTGGGAGTGACAGTG | 68519 |
| rs218928746 | in-del | -/AGCAGGGGA | | | intron-variant | Eml1 | Mm_Celera | 12:108451401 | CAGACTGAGCTCTGG[-/AGCAGGGGA]AGCCTTGGCTAGAGA | 68519 |
| rs218930686 | in-del | -/TTCTTTATTCTTTA | | | intron-variant | Eml1 | Mm_Celera | 12:108478365 | AGAATGTTTAAAGAT[-/TTCTTTATTCTTTA]TTCTTTATTATTTAT | 68519 |
| rs218931239 | snp | A/C | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422334 | TCTCTAGCTTTCTCG[A/C]TTGTCACTTGGCATT | 68519 |
| rs218932756 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108505648 | GATATATTTTGATTC[C/T]GAGATTGTATATACT | 68519 |
| rs218966572 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108427008 | GTACACGCGCTTAAC[C/T]ACTAAGCCATCTCTC | 68519 |
| rs218978114 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108497663 | TAGCAATGTATCTGC[-/TT]TTTTTTTTCTTTTTT | 68519 |
| rs218993455 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502151 | GATGGGGACCCTCTG[C/G]AGCAGCCGGCCAGCC | 68519 |
| rs218996315 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108493722 | TCTGTCACCCTACTC[A/G]TGCAGCCTACAGCAG | 68519 |
| rs219006259 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108431372 | CCTCAGCACCTATAT[C/G]CAAAGCCAGGGACAG | 68519 |
| rs219017439 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402758 | agctcccgctctgtt[C/T]tcagactagcacatg | 68519 |
| rs219023567 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108425851 | TGTGTGTGTCTGTGG[G/T]GTGTGGGGCAGTGCT | 68519 |
| rs219048019 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474418 | TGTGGGACCTTCGGA[A/G]AGATCTCAACCTTTT | 68519 |
| rs219052209 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476461 | ATCTAAGTTGTAGGT[A/G]TTAATTGTAGGTCAT | 68519 |
| rs219062333 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108527830 | AGTTGCAGGGAGCAG[C/T]TAGACGGCTGAGCCT | 68519 |
| rs219084550 | snp | C/T | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370456 | GATACCCCTGGGAGC[C/T]ATGGCCCTACAGCAG | 68519 |
| rs219093244 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108483290 | ACCCAGAGATGAGCT[A/G]TGTTATTGTGAGGCC | 68519 |
| rs219106065 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500935 | GTCTCCCGGTGTCCA[A/C]TCACACCAAGCCACA | 68519 |
| rs219130739 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108448346 | AAATCCTGAGCTGTA[A/G]CCCCAGCCCACTCTC | 68519 |
| rs219136497 | in-del | -/ACAGATACAT | | | intron-variant | Eml1 | Mm_Celera | 12:108390778 | AACCATACACACCAC[-/ACAGATACAT]ACAGATACATATACA | 68519 |
| rs219141480 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369436 | CTGGCATAGGACACG[A/G]CATGGGCCAGGCCAG | 68519 |
| rs219145299 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380599 | TGCAGGTATCGCATG[A/G]CGATCGATCGTATGC | 68519 |
| rs219166427 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454838 | AGCCACTGTCTCCCT[C/T]GTTTTCTGAGCCTGT | 68519 |
| rs219171544 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108506915 | ATCATTAAAATTGGT[A/G]TCTTAGTCAGGGTTT | 68519 |
| rs219192009 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108463340 | GGCAAGCCCATAGAG[C/T]GTGCGTGATGCTGGT | 68519 |
| rs219195798 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471280 | AACAGGAGAAGGATC[A/G]GCAGGAACTGAGGAG | 68519 |
| rs219197218 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508209 | CCAGGATCCACTTGA[-/T]TGGGAGGAGAGGGCC | 68519 |
| rs219204210 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475557 | TTCTCACCCTCCGTC[A/G]TGTGGGCCCTAGGGA | 68519 |
| rs219204885 | snp | A/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409796 | ctctctctctctctc[A/T]cacacacacacacac | 68519 |
| rs219205475 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108389801 | GAGCCCCTGAGGTGC[-/AG]AGAGAGAGCCCACTA | 68519 |
| rs219226243 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108470813 | GGTAGGATGTCTCGA[A/G]TGCTCTGAGAGGGTA | 68519 |
| rs219235189 | in-del | -/TGGGGCA | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108536149 | GGGTGATCTTCCCTG[-/TGGGGCA]TGGCTCTGAGGACTC | 68519 |
| rs219241508 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108413742 | TATAAGCTGCTATGT[A/G]GATTCTGTGAGTCGA | 68519 |
| rs219248077 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454172 | GGAGTTCTGGTGTCT[C/T]GGTGGAGAACAGACT | 68519 |
| rs219254114 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108425442 | CACAGCGAATGGATG[C/T]CACAGGACAAAGTGC | 68519 |
| rs219257885 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532881 | TAATCCTTGTGGCTT[A/T]TCCAGGGCTACTTGC | 68519 |
| rs219270311 | snp | A/C | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421368 | ATTTCCTCTTCGGAG[A/C]TGCTGGCTTCCTGGC | 68519 |
| rs219272951 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108508624 | TGACTCCAGAGCAAG[A/G]GAGGTTGAGGCAGGA | 68519 |
| rs219276991 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108426626 | GAACTCAGAAATCCG[A/C]CTGCCTTTGCCTCCC | 68519 |
| rs219287321 | in-del | -/TACTTGCCAGGGTTAATGATCGAGATCAAGAACCC | | | intron-variant | Eml1 | Mm_Celera | 12:108460540 | CTGGAGTGGTCAAGT[lengthTooLong]TACTGTGTGTGCCCG | 68519 |
| rs219301133 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108470725 | AGTTGGCCTGTGGCC[A/G]TGTGTGTGAGAGACT | 68519 |
| rs219310788 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471123 | AAGTAGCACACACAA[A/G]CCCCGGGTTTGATCC | 68519 |
| rs219333693 | in-del | -/GTCA | | | intron-variant | Eml1 | Mm_Celera | 12:108463496 | TGTCATGGGCTGTAC[-/GTCA]CTCACCTGACACTTC | 68519 |
| rs219341479 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108497222 | TGACCCTACCTGCCC[C/T]TGGGGGCTGGAGGTG | 68519 |
| rs219350835 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108387015 | AGGGAACAGAACCAG[A/G]TGGGGAGGAGAGCGG | 68519 |
| rs219357475 | in-del | -/CACACACA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108462266 | TGGCATGTATGAGTG[-/CACACACA]CACACACACACACAC | 68519 |
| rs219364624 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108477930 | CCTTGTATAGAGATG[C/T]CTCGGGATTGTGAAA | 68519 |
| rs219368121 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108389146 | TTCAGCCCACTAAGC[A/G]TTTGTGTCTGGCTCA | 68519 |
| rs219373542 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504173 | GCTCGTACTGCTAGA[C/T]GTATCAGTAAGCAAG | 68519 |
| rs219382231 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108465557 | AGGCTCTGGGTTTCT[-/A]AAAATCTCCTTATGT | 68519 |
| rs219392012 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433296 | AGTAGAAGCATTCGC[A/T]GAAAGCATATGGTGG | 68519 |
| rs219413456 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108522299 | TACACAACCAGGATC[A/G]CAGGAAGGGCAGGCT | 68519 |
| rs219427628 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108374345 | TGTTAGAGAGCATGT[C/G]GGGGGGGACTCTGTT | 68519 |
| rs219442975 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108389735 | AGAAGCTGAGCCCCC[-/T]TTAGTAAAACGACTA | 68519 |
| rs219458738 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108478258 | TGACAAACAACACGC[A/G]TTCACCCAGGACTTC | 68519 |
| rs219467517 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108375650 | GGCCGCTGACCGGAT[C/G]ATTGACACTCCGCGT | 68519 |
| rs219491331 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492493 | CCCAGCAGAAAAAAA[-/T]TTTTTTTTCTTCTCT | 68519 |
| rs219515086 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108469192 | AGCAAGCACAGGTCA[C/G]GTCACTTCGCACCCA | 68519 |
| rs219544392 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468397 | AAGAAGTCTGGTTTT[A/G]AAAAACAAAACAAAA | 68519 |
| rs219547469 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108476546 | TCCCTTGGCATGTGA[C/T]TCCCAGTTTCCCAGC | 68519 |
| rs219577187 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474254 | CTCGGAAGGCAGAGG[C/T]AGGAGGATTTCTGAG | 68519 |
| rs219603156 | in-del | -/CACCC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472981 | ATACACACACACACA[-/CACCC]CACACCATACACACA | 68519 |
| rs219604810 | in-del | -/GA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477359 | AGGGAGAGGGAGAGG[-/GA]GAGAGAGAGTTGCCT | 68519 |
| rs219624272 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108476081 | TCCTGATACTTGTGA[C/T]TTTCCTGCCTCCACT | 68519 |
| rs219630688 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108415614 | CTGCAAATTGCCTTC[A/C]GTTTTCCAATTCACC | 68519 |
| rs219636199 | in-del | -/AAAAAA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474505 | TGCTGAATTTAGAAG[-/AAAAAA]AAAAAAACAAAAACA | 68519 |
| rs219647438 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108394942 | TGAACACACACTTAT[A/G]TGCGTATACACTGAA | 68519 |
| rs219672864 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108509499 | GGTCTCTAAGTTTAG[-/A]AAAACGTGCTTTGTG | 68519 |
| rs219674928 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108510260 | AGGTGAGGTTTCCTC[C/T]TTGTCTTTCTGACTT | 68519 |
| rs219698574 | in-del | -/AC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474355 | AAACAAAAACAAAAA[-/AC]ACCTCACCATCATGG | 68519 |
| rs219700820 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442963 | TCAGCTAAAAGTCAA[C/T]GTCACTCTCCTCATT | 68519 |
| rs219710693 | in-del | -/GGCC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433702 | TCTAATGGGGGCTCG[-/GGCC]GCCGGCTGGGGAGGT | 68519 |
| rs219729898 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520081 | GTCTCTGCCAAGACA[C/T]GCACCACAGGTAGAG | 68519 |
| rs219733088 | snp | C/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422108 | GCCTACATCTTTGAG[C/G]ACCAGAGTGACAGAT | 68519 |
| rs219745445 | snp | A/G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108371895 | TACCCTGATGTGTGT[A/G/T]GGATTAGCTACCTGA | 68519 |
| rs219755982 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108371504 | TAGCTGCAGCCTAGC[-/G]GAGGCAGTTTGAGTT | 68519 |
| rs219760640 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519527 | GGACCGCATCTCACC[A/G]AGGCATGGAGCTTGC | 68519 |
| rs219765609 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108493961 | ACAGCCCTGAACTGA[-/T]TTTAAAAAAAAATGG | 68519 |
| rs219769825 | in-del | -/CTAA | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402887 | TCTCCATCTAACCAT[-/CTAA]CTCTTTCCCAGAATA | 68519 |
| rs219774951 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108508467 | TACTTGTATCATTTC[A/T]AAGTGATGTTTAATA | 68519 |
| rs219786909 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108534516 | CGAAAGCAGTATAAG[A/G]TACATTGAAAAACAA | 68519 |
| rs219788966 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108450749 | TGGGCAAGAAGCCAG[C/T]GAGTGTGCACTGTGT | 68519 |
| rs219803690 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378278 | CTCTTTCCATTTTGC[C/T]TTCGAGGTTGACACT | 68519 |
| rs219803810 | snp | C/T | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370725 | AAGCTTCCTATGCCT[C/T]GGAGACAGACAGCCT | 68519 |
| rs219805526 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108378709 | TTTTTTGTAACTCTA[C/G]AGTAATCCACTTCAA | 68519 |
| rs219806943 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108526639 | CATGTGGCTCAGCCA[-/C]CCAGCTCAGGCTGAC | 68519 |
| rs219831951 | in-del | -/GCCACGCCAC | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408707 | TTTCTGGCTGCCCTG[-/GCCACGCCAC]GCCACGCCACCCCCA | 68519 |
| rs219837472 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527328 | ATCTCTGTGGCTCCA[A/G]TGTCCACTCCTGAAC | 68519 |
| rs219838376 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108507951 | AAATTGAGTAGTTTT[-/A]AAAATCTAATCTGGA | 68519 |
| rs219839408 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429038 | TACAAATTTGTTTTA[A/T]TTTCCATTTATTTCT | 68519 |
| rs219869430 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108453588 | ATTGAGCCATGTCCC[C/T]AGCTCTTCGTCAGCT | 68519 |
| rs219881449 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502893 | TTTAGCATATTAACT[A/G]TATTTTAAGATATAG | 68519 |
| rs219894690 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479478 | CTCTATTGTTCCTTT[A/T]CCTTTTAGTGGATTT | 68519 |
| rs219899774 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108471556 | CTGGGGAGGAGGAGC[A/T]GGGGAGGAGGGACAG | 68519 |
| rs219925218 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108435231 | TACAGCTTGAGCCTT[A/G]GGAAGTGCCCAGGCT | 68519 |
| rs219925911 | snp | C/T | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | GRCm38.p3 | 12:108400693 | ATTAAACCGTCATAG[C/T]CTCAGGAAGGTTGAG | 68519 |
| rs219927225 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392667 | CCAGTATATAAGAGG[C/T]GCTTCATCAAACCCC | 68519 |
| rs219933934 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108509578 | GGGGCGCAGTAATTT[-/A]AAAAAAGAAAAAGAA | 68519 |
| rs219934828 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108459780 | GAAACAGACAAGCTA[C/T]CTTTTATGCCATTTT | 68519 |
| rs219965595 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108480354 | TTCCTTCCTTCCTCC[C/T]TCCCTCCCTCCCTCC | 68519 |
| rs219970426 | snp | C/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478643 | GTATAGCCCTGGCTG[C/G/T]CCTGGAACTCACTTT | 68519 |
| rs219986053 | in-del | -/TTT | | | intron-variant | Eml1 | Mm_Celera | 12:108510997 | GGACAGGAACCTCCA[-/TTT]TTTTTTATCAATGTG | 68519 |
| rs220052668 | in-del | -/AC | | | intron-variant | Eml1 | Mm_Celera | 12:108399620 | AACTCTAGCTTAGGG[-/AC]AGGTCCTTGCAGGCC | 68519 |
| rs220068046 | snp | C/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108509540 | GTGGTGGGCGGGGCC[C/G/T]GGGTGGTGGGCGGGG | 68519 |
| rs220076045 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429134 | TGGTGTGTGTGTGTG[C/T]GTGTGCGCGCGCGCA | 68519 |
| rs220083959 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108535392 | GGGTCGTGGGGGGGG[-/C]GGGGAGTGGGATGTG | 68519 |
| rs220092175 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108434432 | GTGTCATTATTGCTG[A/C]AGCCTGGATATGGAT | 68519 |
| rs220093317 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532187 | TATTTGTGTGAACAC[-/T]TTGGTTTGGTTTGGA | 68519 |
| rs220106598 | in-del | -/A | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406486 | CACTCCACCCACCCC[-/A]GCACCCCTCCCCCCC | 68519 |
| rs220119230 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108530613 | GGGTTTCTCTGTGTA[G/T]CCCTGGCTGCCCTGG | 68519 |
| rs220131616 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532095 | GGCCTGGGTCACTGC[A/G]CATGCTGACATTTAG | 68519 |
| rs220134648 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108525380 | ATATATTTCTTAAAG[A/G]TTCATTTTTAATATT | 68519 |
| rs220158253 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378306 | ACTCATGAGAATGGC[C/T]TCTTGGGTGTCACTG | 68519 |
| rs220166768 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108531407 | CATCTGTAGTCCCAG[C/T]ACTCAGGAGGCAGAG | 68519 |
| rs220177317 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108430487 | AACTCCAATTCCAGG[A/G]CTTCTGATTCTCTCA | 68519 |
| rs220195439 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108428496 | GTTTTTGTTTGGGGG[G/T]AATTTCCTTTGTAGG | 68519 |
| rs220227278 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108398419 | GAGAGGTTGGGCAAG[C/G]ACATGATAGGGAGGC | 68519 |
| rs220230025 | snp | A/C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108491313 | GTCACTCCCCCCCCC[A/C/G]CCCCCCAGTGCAAAT | 68519 |
| rs220233007 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108475055 | AAAGCAAACCCACAG[C/T]CAAGTCCCTGTAAAG | 68519 |
| rs220236264 | snp | A/C | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108536202 | GGCCTGAGCTGAGAA[A/C]TCACAAGGCTGTTGC | 68519 |
| rs220244833 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108526661 | CAGGCTGACTCCCAA[A/G]CCCAGGCCAGGTTGT | 68519 |
| rs220255894 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108436731 | TACATTCTCTCTGCA[C/T]TAGCTCAGATACTAA | 68519 |
| rs220282743 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404491 | GTGGAGAAAGGGAAT[C/T]GCTTGAGAAAATGCA | 68519 |
| rs220284155 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108397473 | CTGCCTGCAACTCTC[C/T]GCCTCTGTCATGTCA | 68519 |
| rs220297024 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402996 | TCATTAGCCATAAGC[A/G]TTTTTATTGACAGGC | 68519 |
| rs220308510 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108398248 | ACCACTGAGGGAGGT[A/G]GGTGGATAGAGCAGT | 68519 |
| rs220313767 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479668 | TCATATTTTTAATTT[C/T]TTTATGATTCGTTCT | 68519 |
| rs220347292 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532797 | CAGTTTAATGATACC[A/G]GTCTATTTGGAACTT | 68519 |
| rs220363475 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108379720 | AACTCACTCCGTAGA[A/C]CAGGAGTTGACCTTA | 68519 |
| rs220367652 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473667 | CAGTATATGGTGGGG[A/C]CCCTGTGGCTGTTGG | 68519 |
| rs220368452 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108509325 | AGCCAGGGGTGGGGT[G/T]GTGCAGGGCTCTGAA | 68519 |
| rs220368468 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108502268 | CCTCAGACCTCCACA[C/T]GAACATGCACACACG | 68519 |
| rs220407727 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480439 | TGGGAATCACACCCA[A/G]GCCCTCACAAGTGCT | 68519 |
| rs220410194 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108530652 | CTGTAGACCAGGTTG[A/G]CCTTGAACTCCTAGA | 68519 |
| rs220443445 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486508 | GCAACCTCATTCATA[A/T]GGGCTTTCCCTACAC | 68519 |
| rs220446152 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108431864 | CTCCTCCAGACTCCG[C/G]CCTCAGCCCCCTCCA | 68519 |
| rs220459594 | in-del | -/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407083 | TAGTACACATTGAGG[-/T]TTTTTTGTTTTGTTT | 68519 |
| rs220463162 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108423940 | CAGGGTTGGGAAAGA[-/T]TTTTTCACCGCGCTC | 68519 |
| rs220466964 | in-del | -/TC | | | intron-variant | Eml1 | Mm_Celera | 12:108381739 | CCAGCTGAGAAGTCT[-/TC]TCTCCAGTTTCAAAA | 68519 |
| rs220498576 | snp | A/C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108534539 | AAAAACAATGTTTTC[A/C/G]CAATGTTTTCCTTTT | 68519 |
| rs220500594 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447092 | ACCACCTATACCTCA[A/T]GGATCAGCATTGCCC | 68519 |
| rs220501942 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108438198 | GGCTGGCTGTGTATA[A/G]CCTGTGTTCACAGGT | 68519 |
| rs220518422 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404949 | ACACGTATGCATGCA[C/T]ATACACACATGTGCA | 68519 |
| rs220526270 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379649 | TATTTGAGTTTCTTT[C/T]TTTCTTTGATCCTAT | 68519 |
| rs220529810 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454079 | GCAGACAACCTGGTG[C/T]GCAGAAATGAAAAAC | 68519 |
| rs220534608 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108518020 | AGAGAGATCCCATCT[-/A]CAAAATAAATAAATA | 68519 |
| rs220546086 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108395443 | AGTGCTGGAGTGGGG[G/T]AGGGGGAGTGGATGC | 68519 |
| rs220559972 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108429949 | CGGCTCCAAGCCTCG[A/C]GCGTTCTGAAGGCGT | 68519 |
| rs220560425 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503625 | TGTCCCCGTTTATAG[A/T]ACACGATGGCACATA | 68519 |
| rs220561811 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379032 | TGTGTCTATTTTTAA[-/T]TTTTTTGAGGGACTA | 68519 |
| rs220581934 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474291 | GCCAGCCTGGTCTAT[A/G]AAGTGAGTTCCAGGA | 68519 |
| rs220583024 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108446481 | TATGGCATGGTCTCT[A/G]GTCCTAGCACTTGGG | 68519 |
| rs220583174 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108453552 | ACTCCAGTTCTTCTG[A/C]TTATACAGCAGGCTC | 68519 |
| rs220629868 | in-del | -/CAGACACGGGTA | | | intron-variant | Eml1 | Mm_Celera | 12:108535790 | TGTCTAAAACCTACC[-/CAGACACGGGTA]CATAGGCTACCAGTG | 68519 |
| rs220635790 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407965 | CCTCTCCCTCCTCCT[C/T]TCCCTCCTCCTGATT | 68519 |
| rs220636056 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108487241 | AGTTTCCTGTTCCTA[-/T]TAGATACAGAATGCC | 68519 |
| rs220650173 | snp | A/C | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108400855 | CAAACAGAAATGGCC[A/C]TGCACACCTGTCCTG | 68519 |
| rs220653509 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436112 | CCCCTGCCCCCTATG[A/G]TGGCCGTTCTACTTG | 68519 |
| rs220684028 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108458445 | CACAGGAGGATCATG[A/G]TTCCGGCCTTAAAAT | 68519 |
| rs220705419 | snp | A/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406570 | CTTGTACTAGTTAGC[A/T]CTCCCTGTCACTAGG | 68519 |
| rs220714727 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108481664 | AGACTAAGACCCTGG[G/T]TTTCGTTTTGTTTTG | 68519 |
| rs220730876 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504831 | ATTTATTAGAATACC[A/G]AAGTATTTTTGGGTC | 68519 |
| rs220734803 | in-del | -/CAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108459875 | AGTAAGGAAGAGGAG[-/CAAA]CTATAAGGTTGTCTT | 68519 |
| rs220735808 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532119 | CATTTAGTAACCTTC[C/T]GACAGAATTCACGTG | 68519 |
| rs220738450 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476726 | GTAATATCTTTATCA[C/T]AGCAGGTTTAAACTC | 68519 |
| rs220738469 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484460 | GTTCCCGCTGGCTCT[A/T]CCCATCATCCACATA | 68519 |
| rs220740274 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108513320 | ACAAACCCAGGAAAC[C/T]ACTATGTGCTGGGCT | 68519 |
| rs220744367 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477683 | TCGCTAAGTAAGCAT[C/T]TCTGACGTTGTAATA | 68519 |
| rs220753525 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108395048 | TTTAATGAGAAAAAA[-/AT]ATATATATCAGAGTT | 68519 |
| rs220764717 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417043 | TATGATGGGAAACTG[-/T]TTTTTCCCTGGAGGA | 68519 |
| rs220778117 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451697 | TTGTTTTCCCAGTGA[C/G]ATGATTTTCTCTGGA | 68519 |
| rs220822877 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108392693 | ACCCCTGCATCCCCT[A/G]GGCCAGCAGGCACCT | 68519 |
| rs220843923 | snp | C/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108539034 | GCCTTGCTGTGTGTG[C/T]TCTGGACACTGTACA | 68519 |
| rs220862855 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451079 | CGTTTGATTGTTTAT[A/C]ATGTAGATATTTAGA | 68519 |
| rs220865472 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449494 | CTGTGTCCTCGAAAG[A/G]GTCTTTAGACAGCTG | 68519 |
| rs220872031 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108398434 | GACATGATAGGGAGG[C/T]TACAGGATGAGAACA | 68519 |
| rs220876273 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108489830 | CGTGGACTCATCTTC[-/T]TCTCAGACTATGAGT | 68519 |
| rs220892160 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108531766 | CACATTCCTCTAATA[-/G]GATACTGTTGGCATG | 68519 |
| rs220897089 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108457819 | TGTCAGCCTTGTGCC[C/T]TGAGGCATGGTGGGA | 68519 |
| rs220897963 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527861 | CCTGGGGCGGGGGCA[-/G]GTGCATGGCAGCTCT | 68519 |
| rs220913383 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108420003 | AAAATGTTTGGGCAC[-/A]AAAAAAATCACACAT | 68519 |
| rs220928467 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108469999 | ATCTTTTGTCCATTA[-/T]TTTTTTTTCCATTTT | 68519 |
| rs220946462 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455688 | CTTCTGCTCTGGGTT[A/G]GATCTTGCCATGACT | 68519 |
| rs220952549 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404719 | ATGCACGTGCAAATA[C/T]ACACACATGCATGTG | 68519 |
| rs220976069 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108456919 | TTCTCCATATAAGTC[A/G]GGAGACACTAGTAGC | 68519 |
| rs220977624 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460333 | CAATGAAACACAGGC[C/T]TGAAAAACTTCAAAA | 68519 |
| rs220980038 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455386 | CACACCCTTGGGTGC[C/T]AGCACAGGGTCACAG | 68519 |
| rs220991350 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108382104 | AGCAACCAACCAGCC[G/T]AATATTGTTCTGATT | 68519 |
| rs221002897 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108425646 | TGTTCACTCGTTTAA[C/G]TAGAAATCTTGTACA | 68519 |
| rs221013081 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379563 | ATGGCTGTCTGAATG[C/T]CCTCTTTTGAGAAGT | 68519 |
| rs221029162 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108382014 | CTGCCATCTCTGCCT[-/G]GGGAGGCTGGCCCAG | 68519 |
| rs221039589 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108396957 | CAATTCTTTATGTGT[-/G]TTCCCGGGTGACTTC | 68519 |
| rs221043022 | in-del | -/GTGTGAGAGTGTATGTGA | | | intron-variant | Eml1 | Mm_Celera | 12:108449651 | TGTGTGTGTGCATGT[-/GTGTGAGAGTGTATGTGA]GTGTGTGTGCGTGTG | 68519 |
| rs221054910 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108535595 | AAGTTCAGATGCCAG[G/T]GGGGGGCAGAAAGGC | 68519 |
| rs221057332 | in-del | -/CG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108434628 | ACCACACTTAACACA[-/CG]CACACACATCATTTA | 68519 |
| rs221057918 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108424374 | TTGGTATTCCGCCGA[C/T]CACTGGGATACTTTA | 68519 |
| rs221065373 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108501326 | GGACAAATGGCTGGT[A/T]CTAGCCCTTCTGTTG | 68519 |
| rs221074029 | in-del | -/C | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369569 | TCCTGGAAAGGACTT[-/C]CTTTGAGACCTTGTG | 68519 |
| rs221082859 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478051 | TCAAGGAGCCGGGGT[A/T]ATTAGGTACAGAGGA | 68519 |
| rs221090082 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402581 | TTTTGCCTAGGAGGC[A/G]AGCACTCTGCAAACT | 68519 |
| rs221098736 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408113 | TCTCAGAAATGTCTG[C/T]TCCCTTTTTGGGGGT | 68519 |
| rs221113594 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108439608 | CATCTCTCCAGCCCC[C/T]GCCCCACATAGCACC | 68519 |
| rs221114986 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384456 | TGCCACCCCTCCCTC[C/T]AGGGCTCACAAGTCG | 68519 |
| rs221130375 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454731 | CAGAGATCAGCCTGC[C/T]TCTGCCCACGGAGTG | 68519 |
| rs221145045 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108485003 | ATGTGTGAACAGGAT[C/T]GTGCTCTGTTACTTG | 68519 |
| rs221164453 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507150 | CCCAGGACTACCAGC[C/T]CAGGGATGGCTCCAC | 68519 |
| rs221165886 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108486042 | CAGCCGGCCCCTCTT[C/T]CCCTGCGCCCTCAGC | 68519 |
| rs221189109 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408907 | CATGGAGGAGCCTCC[C/T]AGGCCAGGACTGAGA | 68519 |
| rs221203078 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403535 | ATCTGTGGCTACTCC[A/G]GCTTTTTCCACCCTT | 68519 |
| rs221213325 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454118 | CTCACTTTTGAACAA[A/G]GGCACTGCCCAGTGT | 68519 |
| rs221230892 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108535560 | AAAAAAAAAAACAAG[A/C]AAACAACCTTATGAA | 68519 |
| rs221240670 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452347 | CATGGCACCTGCAGG[C/T]CAGCTTGCACGTGGC | 68519 |
| rs221244754 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460346 | GCCTGAAAAACTTCA[A/C]AAATAGAAGCATCCC | 68519 |
| rs221246660 | snp | G/T | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108536370 | TTTGAATGTACTCTA[G/T]TGCCCGAGACCATAC | 68519 |
| rs221286815 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376440 | TCTCATTACGGATGG[C/T]TGTGAGCCACCATGT | 68519 |
| rs221290358 | in-del | -/GTGTGTGTGTGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433955 | AGAGAGTGTGTGCTC[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs221323718 | in-del | -/ACTG | | | intron-variant | Eml1 | Mm_Celera | 12:108529735 | TTATGTGCCAGCCTC[-/ACTG]AGATCAGTGGGATGT | 68519 |
| rs221324962 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108465808 | ACGGCCCTACACTAC[A/G]TCATGGGGAGGGGGC | 68519 |
| rs221329132 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108459902 | TCTTTTTGTTTCTGG[A/G]ACCAGGGACAGAGCC | 68519 |
| rs221333958 | in-del | -/GTGTGTGTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108487521 | ACACATATAGACACA[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTA | 68519 |
| rs221355883 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108381340 | TCAGGATTAGACAGC[C/T]ACGTGAGGTGGTCTG | 68519 |
| rs221404289 | in-del | -/ACAA | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409734 | CTCTCTTACATACAC[-/ACAA]ACATACTCTCTCTCT | 68519 |
| rs221412787 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108477590 | CTTAATTAAAATTTG[C/T]TTGTATCTTAATTTT | 68519 |
| rs221432395 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108381099 | GGGCTCGGGGCGGGG[C/T]TCGGGGTTCAGGGCG | 68519 |
| rs221433294 | snp | G/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408684 | GCAAATGACCATGGC[G/T]TCTCAGAATTTCTGG | 68519 |
| rs221438230 | in-del | -/G | | | intron-variant, frameshift-variant | Eml1, Gm33385 | Mm_Celera | 12:108411055 | TCTGGCGTGGCTCCA[-/G]GGGGGCAGGATAGGA | 68519 |
| rs221445985 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108456664 | CGGTAACTCGATCGA[C/T]CACTGGGTGCAACAA | 68519 |
| rs221456940 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108377620 | ACAGGGGAGCCGTTA[G/T]ATATTCAATATGGGA | 68519 |
| rs221456963 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507198 | CTCCCTCCTTGATCA[C/T]TAATTGAGAAAGTGC | 68519 |
| rs221457061 | snp | A/G | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108539080 | GTGGGTCAAGTCGGA[A/G]AGGGACTCTTCAGTA | 68519 |
| rs221476741 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404968 | CACACATGTGCACGC[A/G]TACAACACACAAACT | 68519 |
| rs221478611 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108512271 | CGTTCATGCAGAGGC[C/T]GCAGTCAACCTCTCC | 68519 |
| rs221500404 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108380623 | CGTATGCTGTCCTGG[A/T]GTTGGTCCCCACCTC | 68519 |
| rs221516671 | in-del | -/AAA | | | intron-variant | Eml1 | Mm_Celera | 12:108467998 | TGGTCCAGGTAGTCC[-/AAA]AAAAAAAAAATGGCT | 68519 |
| rs221543391 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108386335 | CTCAAATACTTATTG[A/G]GCAATATTGGGCCTC | 68519 |
| rs221545309 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108475717 | TTTGGTTTTATTTGT[A/G]TGAGTGTGCCTGAGT | 68519 |
| rs221573050 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482668 | CTCCAGCCCCCGTAA[A/G]GATGTTTTTAAAGAT | 68519 |
| rs221599453 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412702 | TCACACCTTTAATCC[C/T]AGCACTTGGGAGGCA | 68519 |
| rs221602469 | in-del | -/CT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108417604 | AGCCTAAAAGGATCA[-/CT]TTTTTTTTTTCTTTT | 68519 |
| rs221606113 | in-del | -/ATGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108467803 | AGCACGTGGATAGAG[-/ATGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs221628720 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482185 | AGGCTCTGAGTTCAT[A/G]TCCTCAGCACCCCAC | 68519 |
| rs221654323 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108489558 | TGGAGAGATGACTCA[G/T]CAGTCAGGACCACTG | 68519 |
| rs221672929 | in-del | -/GTTG | | | intron-variant | Eml1 | Mm_Celera | 12:108433758 | GTGGGGAGGAACAGA[-/GTTG]GTATGCACTCATGGC | 68519 |
| rs221711883 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488588 | GGCAATCACAGGTCA[C/T]ATCCTGGAAACTGTA | 68519 |
| rs221717623 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108378788 | TGCGTTGTAGGTCAC[A/G]TGACTCTCAAAATGC | 68519 |
| rs221729910 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108517249 | GGTTCTCCTGGTTAC[A/G]TGGCAGACAAAGGCT | 68519 |
| rs221766267 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108383001 | GTTTCTGGCTGTTTA[A/G]TACATGCTATTTAGC | 68519 |
| rs221782395 | in-del | -/CT | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408312 | ACAATCACGCACACA[-/CT]CACACACGTGCACGC | 68519 |
| rs221784281 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451820 | CTGGACATTGTATGG[C/T]CAGGATAGGGAAATA | 68519 |
| rs221794444 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108384495 | GGAGGCGGATGGAGC[A/C]AGGCTTCTGTTGTGT | 68519 |
| rs221800306 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108405617 | TCCTTCTGTCACTGC[C/T]CACATTTTTTGTTGT | 68519 |
| rs221806415 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108382140 | GAAACAAATTTCAGT[A/G]AAAACTTAACAGTCT | 68519 |
| rs221807166 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108389017 | TGGTAAGTACTTTAT[C/T]TCCCAAGCCCTAGAA | 68519 |
| rs221864649 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480389 | CTTCCTTCCTTCCTT[C/T]CCCGTTTTTGTAGTA | 68519 |
| rs221874006 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410799 | ACGGCCAGGAGGACA[C/T]GAGAGGCACAGTCTG | 68519 |
| rs221883030 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108384275 | AAATGCATCACTTCC[A/C]TTTGCCTGAGCCAGG | 68519 |
| rs221885869 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485047 | CACTCTAAGGATGGC[G/T]AGATTTGTCAAAAGC | 68519 |
| rs221920109 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108461255 | CCAGGGGATCCAACA[C/G]CCTTTGCTGGTGTGT | 68519 |
| rs221930635 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108458449 | GGAGGATCATGATTC[C/T]GGCCTTAAAATGACA | 68519 |
| rs221953315 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108510945 | CAGCCTCTTAAGTCC[C/T]TGTTTGTACAGCTTT | 68519 |
| rs221963267 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492475 | AGCCCGCCTCTTCTA[C/T]TTCCCAGCAGAAAAA | 68519 |
| rs221979616 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108441630 | CTTAGACATCTTGAG[C/T]TCCAGCCCACAGCTC | 68519 |
| rs221994751 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108518759 | GCTGCCCTGGAATTC[C/T]CTCTGTAGACCAGGC | 68519 |
| rs222004369 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412794 | ACAGAGAAACTATCG[-/AA]AGAGAGAGAGAGAGA | 68519 |
| rs222047686 | snp | A/G | | | intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108537914 | GATTTCAGACCTATC[A/G]TGTGCTGTTCTCTGT | 68519 |
| rs222052206 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108441086 | TAGGTCCTGGGATAT[C/T]TTCACAGAAGATTTG | 68519 |
| rs222067656 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108430618 | GTACAAGGTGGGTGT[A/G]CACTCCCTGTAATCC | 68519 |
| rs222070782 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108437478 | TTTCCCACCTGTTGG[A/G]TCCACCAATGTAGCT | 68519 |
| rs222079944 | snp | C/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536975 | TCCCAGGACACAGTG[C/G]CCCTATTCTCCAGGT | 68519 |
| rs222083646 | in-del | -/GAGT | | | intron-variant | Eml1 | Mm_Celera | 12:108498750 | GGATCCTGGGAACTG[-/GAGT]GAGTTAGAGATGGCT | 68519 |
| rs222086709 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108390037 | GCAGCTGCTACCCTT[-/A]AAAAAAAAAAACACA | 68519 |
| rs222095563 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108533261 | CTTCCCAGTTCCCCA[C/T]GTGCATTCTCTGTTC | 68519 |
| rs222107803 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108377294 | GTGCTGAGGTATTGG[A/G]TGTTTGGGGACAACT | 68519 |
| rs222128111 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436903 | TGACACGAACGCCTG[A/G]TTGGGGCTTCCAATT | 68519 |
| rs222170109 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455824 | GGCACAGTATGTGTG[C/T]ACAGACTCTGAGCCT | 68519 |
| rs222175528 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532844 | ATAATTTGTTAGCAC[C/T]GACATGTACAGCATT | 68519 |
| rs222179687 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403115 | AGGCAGTTCCCACCA[A/C]TGATTTCCAGAACTG | 68519 |
| rs222180056 | snp | A/G | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411576 | CAGCCATGGGCATGG[A/G]TCCTGCTTGTTTGGG | 68519 |
| rs222197094 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108505910 | GCATTAGATTTTAAA[A/T]TTTGATTTAATTTTT | 68519 |
| rs222234839 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108513394 | GCTCAAGACCAGCCA[C/G]TCTGTGGGACTGCAG | 68519 |
| rs222240600 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442584 | TGTGCCAGAAGAGGG[C/T]GTCAGATCCCATTAC | 68519 |
| rs222247533 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108444991 | TTGTCCCACTCTTCT[-/C]CCCCACACAATTGCG | 68519 |
| rs222253719 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405578 | GCCTGCATGTTTGCT[A/C]TCATGTGACAACCTT | 68519 |
| rs222262777 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489669 | GCTTTGACACCCTCT[A/T]CCTGGGCCCTGCACA | 68519 |
| rs222274616 | snp | A/G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406309 | TTTGATTTCAGACTC[A/G/T]GCACAGTTGTACGAT | 68519 |
| rs222280113 | in-del | -/GT | | | intron-variant | Eml1 | Mm_Celera | 12:108496950 | TTGCTTTGGGTCACA[-/GT]GTTTCGTCACAGCAA | 68519 |
| rs222292638 | in-del | -/TC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473035 | CATCAAGCATACACA[-/TC]TATCTCTCTCACACA | 68519 |
| rs222294520 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108534602 | CAGCCTTTCCTCTTA[-/C]GACAAGTGATGTCAC | 68519 |
| rs222295412 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507834 | CGCTGACAAGAATTA[A/G]TATTTGAGATGGTGG | 68519 |
| rs222297931 | snp | C/T | | | synonymous-codon | Eml1 | Mm_Celera | 12:108516602 | AAACTATCAAAAACT[C/T]CACAAAGCAGAGGTA | 68519 |
| rs222345422 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108443546 | CCAAATTCCTGCAGC[A/G]GTTGTGCTCTCCACC | 68519 |
| rs222368008 | in-del | -/CCTGGTTGAAGGCATCCA | | | intron-variant | Eml1 | Mm_Celera | 12:108440994 | TCGGGTTCACCATCT[-/CCTGGTTGAAGGCATCCA]CCTGCTTCATGTCTG | 68519 |
| rs222381649 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405018 | TTAACTAAAACTCCA[C/T]TTTATATTTATTCTT | 68519 |
| rs222409668 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108380638 | AGTTGGTCCCCACCT[C/T]GGAGATTGTTTCCTT | 68519 |
| rs222450766 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108440579 | AGTTTGGTCTCATTT[C/T]CCAGCTCTCGCTGCT | 68519 |
| rs222450871 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433105 | CTTACTGTGAGACGC[A/G]AGATCCTGTACACAT | 68519 |
| rs222454935 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460355 | ACTTCAAAAATAGAA[A/G]CATCCCTGGTCCGAA | 68519 |
| rs222464539 | in-del | -/TA | | | intron-variant | Eml1 | Mm_Celera | 12:108532430 | TGTAATCATCGCCGG[-/TA]TACACTTGGCTGCGG | 68519 |
| rs222474737 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464987 | ctcCTTGCTTttttt[G/T]tttgtttgtttttgg | 68519 |
| rs222480016 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108510433 | CACCCTGAGCTTCCT[C/G]ATAACTTCAGCCAGT | 68519 |
| rs222504602 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108386384 | CTGTATAAGGGGACA[A/G]TGACAGTATCTGTTT | 68519 |
| rs222504968 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108439881 | TCTTAAAAAAAAAAA[A/G]GAAAAAAAAATTCCA | 68519 |
| rs222542865 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108414761 | GTTCTGTGGATCCCC[A/G]TCTCCACATCACTCT | 68519 |
| rs222546270 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466392 | GGTGCTTCCACCTCA[C/G]TATTTGGGGTGCTTC | 68519 |
| rs222557281 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437568 | GCGGCACGCTCAGGG[C/T]GCCGAGCTTCATCTC | 68519 |
| rs222557614 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480836 | TGTGATCACAGCTCC[A/C]AATGAAGCAAGCCAG | 68519 |
| rs222562166 | in-del | -/ATATGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108486680 | GTCTATGGGATTCCC[-/ATATGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs222562234 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451291 | CAATCATGAGTGCAC[A/G]CGCACACACACATGT | 68519 |
| rs222569646 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108518176 | ACCTACATGGCCCTC[A/G]CAAACATCTGTTGCT | 68519 |
| rs222586652 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535591 | TAGAAAGTTCAGATG[C/G]CAGTGGGGGGCAGAA | 68519 |
| rs222609907 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108414099 | TGTAGGAATATTTTC[C/T]TTATGGGAGATTTAT | 68519 |
| rs222613763 | in-del | -/AGGCACCCATACACACACACACACAC | | | intron-variant | Eml1 | Mm_Celera | 12:108485361 | CACACACACACACAG[-/AGGCACCCATACACACACACACACAC]AGGCACCCACTCATT | 68519 |
| rs222618158 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108462779 | GGAAGGTGTCCAGGG[C/T]TGGGAACTGTGCCTC | 68519 |
| rs222628411 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108512001 | GGCTTCCAGCCTTTC[G/T]CAAGGCATGCTAGCC | 68519 |
| rs222655020 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108478194 | CCAAGGAAGGCTCTG[-/C]CCCTGTCATGGGGCC | 68519 |
| rs222661573 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460185 | TTGCGATAACAATAA[C/G]GTTAGCAGCAGTGGG | 68519 |
| rs222670209 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519308 | TTCTGGTACCTTAGA[C/G]GACATCATTCACCAC | 68519 |
| rs222673414 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108409555 | CATCCCATACATATA[C/T]TTCCTCTCTGTCTCT | 68519 |
| rs222679173 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108490717 | GTGTAGCCAGTGAGA[A/C]AGAATGGAAAGCACA | 68519 |
| rs222713275 | in-del | -/ATCA | | | intron-variant | Eml1 | Mm_Celera | 12:108534965 | CTGTGAGTAACAGGC[-/ATCA]ATCAGGCTTGTCGGG | 68519 |
| rs222736945 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108461921 | CCTACTTTTCTGGTG[A/G]AGAAGTTGAGGTATC | 68519 |
| rs222743816 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108457657 | AAATTCTACCACACA[C/T]TCCACTGCAGCCACA | 68519 |
| rs222760318 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108512555 | AAATAATCAGGGATA[A/G]AGAGATGGTTAAGAA | 68519 |
| rs222763756 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108431639 | CACAGACACGGACAC[A/G]TATACACAGAACTCA | 68519 |
| rs222764928 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108479791 | CTGTGTGTATCTGGG[A/G]TGACATCACTGGGGC | 68519 |
| rs222768911 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108487537 | GTGTGTGTGTGTGTA[C/T]GTGTACATATACATA | 68519 |
| rs222781770 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108456898 | CTGGTGGTGAATCCT[A/G]GTGGATTCTCCATAT | 68519 |
| rs222803674 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486529 | TTCCCTACACTCTTG[A/T]CCCCCCTGAAGGACC | 68519 |
| rs222819564 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475503 | CCAACACGCCGTGGT[G/T]GTCCACGCAGAGGTC | 68519 |
| rs222819720 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437935 | CCGGGATTCACACAC[C/T]CTGTAACAGCGCTGG | 68519 |
| rs222848980 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108384008 | GCCTCAGAGCTCACC[C/T]ATCATAAACCATACA | 68519 |
| rs222894346 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500570 | TTAGCTTGCCCCAAG[C/T]CGACTCTTCTTGCTT | 68519 |
| rs222895507 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108515984 | ACCTTCCTGTCTTCC[C/T]GGGTCTCAGAGTTAG | 68519 |
| rs222907110 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108385870 | ATCGGGAGGGCACAT[A/C]CCCAACAGCACTCAC | 68519 |
| rs222934338 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437030 | TAGAACGTTCTCTGG[A/G]ACTGACAACAGATAA | 68519 |
| rs222940406 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524047 | ATTTCATCCTAAAGC[A/T]ATATATATATATATA | 68519 |
| rs222975475 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482341 | GAGGAAGACTCCTGA[C/T]GTCCTCTGGCCTACT | 68519 |
| rs223018367 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418708 | GTGTGTACACATGGG[C/T]GTGAATATGCTTATG | 68519 |
| rs223055593 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108430756 | CCACCTGCAAAAAAA[-/AT]CCCCAGGTAGACACA | 68519 |
| rs223073256 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108512710 | TGCACATTTTTTTTT[-/A]AAAAAAGTAATCCCC | 68519 |
| rs223090726 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437998 | TGTGGTTTGCTCTGA[A/G]TCGCCTCGAGACATA | 68519 |
| rs223139223 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524348 | CTATCAGATTACCAT[A/G]GCCTAAGGCTGATCT | 68519 |
| rs223164351 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486316 | ACCTGCTTTACCACC[A/G]GGCCATGGTCTGTTG | 68519 |
| rs223164732 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108494823 | ACTTCCTCTTCTTGG[A/C]GGACCATTGTCTATA | 68519 |
| rs223165387 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393335 | TCACCTGTGAAGACC[A/G]GGTGGAAGTTGAGAT | 68519 |
| rs223171340 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108485084 | GTTAGGCGGCCTTTA[C/T]AGTCTTGGCACAAGG | 68519 |
| rs223194364 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442479 | CCTCAGCAGAAAAGT[-/G]AAAAAAATGTGCTTG | 68519 |
| rs223195262 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383188 | CAACTCACACCACTT[C/T]TCTTTATTGCTTTCA | 68519 |
| rs223207977 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436072 | AGTCCCTCTCCACAG[A/G]ATGCGGCCCTGCTCT | 68519 |
| rs223222138 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108490748 | TGGCACGATCTGGAT[A/G]TCTTCACGTTTGAGA | 68519 |
| rs223282620 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442117 | GGGTCCGCCAGAACC[C/G]GACTCTGGAAACTGT | 68519 |
| rs223295690 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440629 | TTCAAGCTGCTGGCT[C/T]AGGTCTCCAAAGATC | 68519 |
| rs223306952 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488248 | TCAGTACACTGGGCA[A/G]TGAAGGACTGTCCCT | 68519 |
| rs223312071 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485986 | ACCACAGGATGAGTC[A/G]CACACTTGTGCATAG | 68519 |
| rs223321808 | snp | A/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538946 | TTAGCCACCACTCTC[A/T]GCGTATTGATGGCAT | 68519 |
| rs223337862 | snp | C/T | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370905 | CACACTCACTGGCAG[C/T]GTCCCTTGGGATCCT | 68519 |
| rs223344583 | in-del | -/GTGTGTGTGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494840 | GACCATTGTCTATAG[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs223368680 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108461836 | ATTAGTTTGTATAAT[A/G]TACTGTAAGTGAAGC | 68519 |
| rs223379058 | in-del | -/CA | | | intron-variant | Eml1 | Mm_Celera | 12:108431552 | CCAGCCCCACACATG[-/CA]CAGACACAGACACGT | 68519 |
| rs223390765 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445774 | CCGATAAAAGCAATT[A/T]TCTTTACCTGTTAGA | 68519 |
| rs223398097 | snp | C/T | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370084 | TGCGACTAAAGATAG[C/T]TACAGTGTACTTATG | 68519 |
| rs223423228 | in-del | -/AACTATCGAAAGAGAGAGAGAGAGAGAGAGAG | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412786 | AGGGCTATACAGAGA[lengthTooLong]AGAGAGAGAGAGAGA | 68519 |
| rs223426513 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471381 | GAGGAGCAGGGGAGG[A/G]GGAGCAGGAGAGGAG | 68519 |
| rs223442410 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108468194 | CCTCCTCCCCCCATG[A/G]CCTTATAGGCTGCCC | 68519 |
| rs223444622 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108493640 | AAGTTAACCGTCACA[A/G]AAGCATTTGGAGTTC | 68519 |
| rs223472658 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108467345 | CTTTAGTTGGAAGAG[C/T]CCCGGGCATTGAACC | 68519 |
| rs223516005 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108475247 | GGGCTTTATCTGCTA[-/T]TTTTTTTTATTGTAA | 68519 |
| rs223516802 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408750 | TTACAGATGGCTCCT[A/G]TTCCCCAGCTGTTCC | 68519 |
| rs223520604 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108529379 | CACCATCCATAACTC[-/T]TGTCTTTCTGGGAGA | 68519 |
| rs223525303 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471092 | TTAAGGAAGTGGCTC[A/G]GTTGGTTGAGTGCTT | 68519 |
| rs223552081 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413093 | TGGAGTCGGTGGATT[C/T]AGTCAGCCACCTATC | 68519 |
| rs223553682 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449581 | ATTAAGGTCAAACAC[-/T]TGTCAGTTATTTTCT | 68519 |
| rs223559322 | in-del | -/CGCGCG | | | intron-variant | Eml1 | Mm_Celera | 12:108462283 | ACACACACACACACA[-/CGCGCG]CACACACACACACAC | 68519 |
| rs223563020 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108416359 | GTTCAGAGGACTAAG[A/C]TGGCTGAGGAGACAG | 68519 |
| rs223570189 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108435495 | TGTGCACGCTAACCC[C/T]GAGCCAGACCAGGAC | 68519 |
| rs223572248 | snp | A/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412465 | ACTAGAGTTGGGCTT[A/T]GACAGGCTGGCTTCC | 68519 |
| rs223577299 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108494755 | TCCTAGAAGCCATTC[A/C]CTCTTCTCAGATTCC | 68519 |
| rs223584795 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108459667 | ATGAAAAAACCCATC[C/T]CAAAAAACCTAAGCA | 68519 |
| rs223587073 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108460089 | TCTAAGTGATCTCAC[A/G]GGGCTGTGCGCTGCG | 68519 |
| rs223592805 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108518248 | GCACTGTATACGTGA[A/G]CACATACATACATGC | 68519 |
| rs223596409 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108419682 | ATTCATTCCCAGCCC[A/T]GAGTGTGGTGCCTGG | 68519 |
| rs223605078 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416136 | CGGAAAACTGGAAAG[A/G]GAGAGAGAGGGTCGT | 68519 |
| rs223613912 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418668 | tctctctctctctct[C/T]tctctctctctctct | 68519 |
| rs223617405 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390387 | AGGGTTTCTGAGATA[G/T]GTAGATGGATAAAGG | 68519 |
| rs223630080 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108514209 | TCCTTGTTGACATCT[A/G]GCTTCCAGCCACACA | 68519 |
| rs223643190 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108415701 | CTTTGAGTAAACAGT[C/T]GATGAACAATTATTA | 68519 |
| rs223646436 | in-del | -/AC/TA | | | intron-variant | Eml1 | Mm_Celera | 12:108434756 | ACATATACCATGTAC[-/AC/TA]CACACACATACATAA | 68519 |
| rs223648375 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441727 | TGGCTTCCTGTGGCT[C/T]CTCTTAGTTTAATGG | 68519 |
| rs223658736 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517613 | GTGCCCTCTTGCCCA[C/T]GGGGCATCTCCCCAA | 68519 |
| rs223666835 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430544 | GGCACAACATCATTG[C/T]ACATAAAATAGAGAT | 68519 |
| rs223671789 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381293 | AGGATAGCATACTGC[A/G]TACATGAAAAGTTGA | 68519 |
| rs223675577 | in-del | -/ACCTGTAC | | | intron-variant | Eml1 | Mm_Celera | 12:108447156 | CGTGCCAAATGTGAG[-/ACCTGTAC]ACCCTTATTTGAGAG | 68519 |
| rs223677994 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384639 | ATTTAAACAGACAGA[A/C]AAACAGGATAAAACA | 68519 |
| rs223686297 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525568 | TAAAAACTTGTTATA[C/T]AAAAGAATATAACAA | 68519 |
| rs223686345 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108516996 | TCATTTCACCACCTG[A/C]GACCTAGACAGCAGC | 68519 |
| rs223703369 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108487648 | ATTCAGGATTAGGAC[A/G]ATATTTCCAGCAGAT | 68519 |
| rs223703956 | in-del | -/TCTG | | | intron-variant | Eml1 | Mm_Celera | 12:108446551 | GTCATCCAGGGAGAC[-/TCTG]TCTAAGAAAAACCAA | 68519 |
| rs223708851 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108513580 | CTCTTGGCATCTGTC[A/G]GCCTCGGTTAACCTG | 68519 |
| rs223725739 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390425 | TTTAATCCTTTGAAC[C/T]CTCTGACTTCCACAT | 68519 |
| rs223725997 | snp | A/G | | | intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538019 | GGGGGCAGTAACGGA[A/G]TTTTAGACTGATTTA | 68519 |
| rs223738042 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520163 | TCTTCCTGCGGTGAA[A/T]GAGCATGCTTTACTT | 68519 |
| rs223786740 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108524616 | GACAGCATACCTGAA[A/C]GCTCTAGAACAAAAA | 68519 |
| rs223794769 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108387176 | TGCCCCTGGTACTAT[A/G]TTCTGGGCCAAAAAG | 68519 |
| rs223795608 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108487784 | AGCTTCTGCCATGAC[A/G]TCTGCGTTTGTCCCT | 68519 |
| rs223845371 | snp | A/G | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | GRCm38.p3 | 12:108411623 | TGACTTGGCTCGTGG[A/G]TTCTCTGCTAGTTAG | 68519 |
| rs223867084 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108440893 | TCCTGTAGTCATGCA[A/C]GGCCTGCTCCCGTCA | 68519 |
| rs223885834 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438789 | TGTATTGGGGGGTTT[G/T]GGGGGAGAAATGAAA | 68519 |
| rs223890834 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446667 | TTCTTTATAAAGCAC[C/T]TTTAAGTTGACAGAT | 68519 |
| rs223895818 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108534024 | CACAGGAGGCTCCAC[A/T]GAGGTGGACCCCCCA | 68519 |
| rs223914330 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486899 | TTGCACTCTCCTAGA[A/G]CATACCTTCCACTGT | 68519 |
| rs223920123 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443609 | CCCACTGGCATCTCG[A/G]CGCTGCTGCCTTCAA | 68519 |
| rs223923612 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108446038 | TGATACCGTCTTCTG[A/G]TTGCCAAGGTAACCA | 68519 |
| rs223943019 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108443987 | GCATATTAAAGCATC[A/G]CATCTTACTCTGTAT | 68519 |
| rs223957615 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416028 | AAACATCTCACAAGC[A/G]CTCACAAGAGGAGAG | 68519 |
| rs223957866 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108424749 | TCTTTGGTAGCTCAG[A/T]CATACAGTTGTTTTA | 68519 |
| rs223959953 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108491602 | TCCCATGACTTCATA[C/T]AATCTTCACCTTCCA | 68519 |
| rs223962242 | in-del | -/GCA | | | intron-variant | Eml1 | Mm_Celera | 12:108503750 | GACCTCAACAGACAC[-/GCA]GCACTATCGGCACCC | 68519 |
| rs223976593 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | GRCm38.p3 | 12:108535940 | CTGTCTAGTGTGCGC[A/G]CACACACCTGTAATA | 68519 |
| rs224024508 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108423633 | AACAAATCACTGCTG[A/G]AACAAAACCTTTGCA | 68519 |
| rs224091152 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108417941 | CTGTCCCTCAGCCTC[C/T]AAAGTGCTGTCATTA | 68519 |
| rs224122669 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108516031 | AAACACAGACCGCCC[A/G]CCCGATGTTACTTCT | 68519 |
| rs224131513 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108520682 | CAGGGTCTCTCTATT[C/T]CTGGCTGACCTAGAA | 68519 |
| rs224137845 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449030 | TGAGCCAGCATGCTA[C/T]CAGCTGAGCCACATC | 68519 |
| rs224137867 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108471158 | CAATGCTGTGAGAGC[-/T]TGACACAGAGGTGCA | 68519 |
| rs224149247 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108415497 | GACACCCTCTTCTGT[C/T]TTGTGCCGGCATCTG | 68519 |
| rs224167105 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462248 | TGACTTCCAAATGTG[C/T]CATGGCATGTATGAG | 68519 |
| rs224173080 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108519735 | TTGAGTCAGGTTCTC[C/T]CTGTGTGTATGTGTA | 68519 |
| rs224194709 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108426413 | CCTTCCACCATGTGG[A/G]CACCAGGGATGAAGC | 68519 |
| rs224206823 | snp | A/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402953 | ctctctctctctctc[A/T]catggaactcccacc | 68519 |
| rs224207590 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524106 | TTCTCCAAAATTGAT[C/T]GTATAGCCGGGTGGT | 68519 |
| rs224213555 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108414922 | GAAACTCTGCTGCTT[C/T]GAGATGGCATTTTAA | 68519 |
| rs224255293 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445120 | GGTTAATTAAGGGAA[C/T]AACATAAACATTTGA | 68519 |
| rs224270387 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527826 | GCAGAGTTGCAGGGA[A/G]CAGTTAGACGGCTGA | 68519 |
| rs224302632 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108393550 | AGAATCAGGGAGTGG[C/T]GCTGTGCTGGGGACA | 68519 |
| rs224332406 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405084 | CTGCCCAAGGCCAGG[A/G]GTAGGGAGCACACAC | 68519 |
| rs224349564 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409707 | ACACACACACATACA[C/T]ACCCAGTCTTTCTCT | 68519 |
| rs224371663 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369456 | GGCCAGGCCAGAGGA[A/G]CCTTTGAAGTTTTGA | 68519 |
| rs224392407 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108392806 | TGATCTCTCTCTCCC[A/G]AGGAGGAGGAGGTCG | 68519 |
| rs224392591 | snp | C/T | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108400945 | CCAGAGCCCAGCTCC[C/T]AGGGGGACCTTGAGG | 68519 |
| rs224433605 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108463310 | AGATGAAGTGCCAGT[C/T]TAGACGTTAAACGTG | 68519 |
| rs224440434 | in-del | -/GT | | | intron-variant | Eml1 | Mm_Celera | 12:108444754 | GAAGAAGTCCAGCCA[-/GT]GAGTGCTCCTGACCT | 68519 |
| rs224453644 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108515020 | ACTCCAGAGGCTGGC[A/G]TGGTCCAGCTGGAGT | 68519 |
| rs224468433 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108470799 | ATCACCATCCCCTGG[A/G]TAGGATGTCTCGAAT | 68519 |
| rs224485888 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108452797 | CTGTCCTTAACAAGT[-/C]TACCTGCAGGGACCA | 68519 |
| rs224490715 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108521794 | GGTAAGTAAGTGTGC[A/G]TGCTGCATTTCCAGT | 68519 |
| rs224492174 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108381483 | AACCAGAACAGAGAC[-/A]ACGTAGAGAGCCCAG | 68519 |
| rs224500653 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441785 | TGCTTTGGTTTTGCC[C/T]TGTCTGTGGTGCAAG | 68519 |
| rs224505497 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108440046 | ACCGGCTTTCGTTGT[A/G]TTGGCACGAAGGGCC | 68519 |
| rs224513612 | in-del | -/C | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536714 | TTATACCCACAGGAA[-/C]CACATGACACTTGAC | 68519 |
| rs224521907 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494076 | GGTGCTTCAGAGTCT[A/G]GAGTGGGAGTGACAG | 68519 |
| rs224525426 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108377427 | TTAGCCACAAATAAC[-/TG]TGCGTGCGTGTGCCC | 68519 |
| rs224531707 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416426 | GCTACCTCTGGGAGG[C/G]CTCCCCAGAAGTCTG | 68519 |
| rs224536298 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451024 | GGAAACCAAGGAGGT[A/G]CAAGGAGGTGCTGAG | 68519 |
| rs224563233 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108441295 | CTCACGCCGACTGCC[C/G]GGGTCCTCGGTAGAA | 68519 |
| rs224573800 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108445216 | TTATAGAAAGTCTGT[A/G]CTTTGTAAAACAAAT | 68519 |
| rs224577869 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108514284 | AAGGTGAAGTCGGTG[A/G]GGCTTGAGAGACTCA | 68519 |
| rs224612636 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447711 | GTCAAATGTCATTCC[C/T]TTGTCTTCATGCTAA | 68519 |
| rs224615504 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376519 | TAAACCACAGAGCCA[C/T]CTCTCCAGCCCCTCT | 68519 |
| rs224634902 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108496362 | GGCTTGTTTGAGCCT[C/T]ACCACCCACTCCACA | 68519 |
| rs224649862 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470360 | TCTTAATGAGACCCA[C/T]ATTGTCAATCCTCCC | 68519 |
| rs224650496 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108444447 | TTGTTTCTGTTCTTC[C/T]GCTAGGACTGACGCC | 68519 |
| rs224674980 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108521446 | CCATCACTCAGGTAT[C/T]GTCAACTTGGCAAAT | 68519 |
| rs224691254 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108438882 | CAAGAATTTGAGGTC[A/C]GTGTGAGTATACAGC | 68519 |
| rs224726658 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469372 | GAGCAGGTCTTCCCA[C/T]TTCAATGAACCTAAC | 68519 |
| rs224732717 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503695 | GCGAGATAAGGAAGC[G/T]TCAGGCACACGCATT | 68519 |
| rs224778458 | in-del | -/TC | | | intron-variant | Eml1 | Mm_Celera | 12:108485801 | ACAGAGCTACCACAT[-/TC]TCTCTCTCTCTGCTA | 68519 |
| rs224805435 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108476782 | TTCCCTCCCTCAGCC[C/T]TGTCTTTTGTTTCTG | 68519 |
| rs224808962 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469037 | AAGAGGACAACCAAG[A/G]CTGACAGTGCTATAT | 68519 |
| rs224817074 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108372922 | TTAGGCCAGCCTGAG[C/G]TACACAGAGAGATTG | 68519 |
| rs224833377 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419506 | TCTTGCCTGTTGGAT[A/G]TACATAAAACTGCAT | 68519 |
| rs224844971 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108476440 | CCTGTACTGTTTTCG[A/G]GGGCTATCTAAGTTG | 68519 |
| rs224849095 | in-del | -/AGAC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108481343 | CTCTGTGCCAGTCTG[-/AGAC]AGAGTCGTGAAGTAG | 68519 |
| rs224854241 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108465691 | GTGACCTAACACCTC[G/T]CTGTGTGCCGCTTTC | 68519 |
| rs224863567 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108478289 | ACTCACGTCCTACAT[-/AG]TGTGTGGGGTTTTAA | 68519 |
| rs224894668 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429089 | TTTAATAGTAATATT[A/T]AAAAATTTTAAATTG | 68519 |
| rs224910495 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108414351 | ATAGATGTCTCTAGG[A/T]GGGGTGTGTGAAGGA | 68519 |
| rs224929042 | in-del | -/CT | | | intron-variant | Eml1 | Mm_Celera | 12:108447953 | TCTGGCCCGGGGTAC[-/CT]CTCTGTTTGGCCCAA | 68519 |
| rs224944781 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473573 | CCATGCCATCTGGGT[C/G]CAGGCCGTGCCTTCA | 68519 |
| rs224960362 | in-del | -/AAGACTCT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450123 | GAGTCAGTGGCAATG[-/AAGACTCT]AAGCACCGGGGTCAC | 68519 |
| rs224972929 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525291 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCTC | 68519 |
| rs224988356 | in-del | -/CTGGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108511367 | TAGAGAGACCACATG[-/CTGGTGT]CTGGTGCCTGGCAAC | 68519 |
| rs224994674 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108466263 | TTGGCATATCCCTGG[C/T]TGGTCCTGGTTGATG | 68519 |
| rs225005927 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108522086 | AGATCTTGGGTGCAA[C/T]TCTGAACCCAGAAGA | 68519 |
| rs225017649 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447765 | TGACCAAAGGCAGGA[G/T]GTCTGCCTGCTTTTG | 68519 |
| rs225019124 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381101 | CTCGGGGCGGGGTTC[-/G]GGGGTTCAGGGCGGA | 68519 |
| rs225042336 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108518022 | GAGAGATCCCATCTC[A/C]AAATAAATAAATAAA | 68519 |
| rs225048719 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474218 | AGCCAGGCATGGTGG[C/T]GCACGCCTTTAATCC | 68519 |
| rs225089985 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525884 | CTTTTAATAATTGTG[G/T]TGCTTTTGAGAATGT | 68519 |
| rs225114796 | in-del | -/AC | | | intron-variant | Eml1 | Mm_Celera | 12:108441697 | GACTCAGAAAATGAA[-/AC]ACATGGTTTTCAGTG | 68519 |
| rs225118912 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108395435 | GTCACTTCAGTGCTG[C/G]AGTGGGGGAGGGGGA | 68519 |
| rs225119016 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108388157 | CAGGGCTCAGTCCCG[A/G]GTGTTAAGGCTTTCA | 68519 |
| rs225120430 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108447306 | AAACGAGGATGAGTG[C/G]ATAGTTCTTTTAGAT | 68519 |
| rs225124353 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108529349 | CCTCCCCCCAACCCA[C/T]ATCAGGCAGCTCACC | 68519 |
| rs225136998 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467398 | TAGCACATTCTCTAT[A/G]TGTGGGCCTGGTGCC | 68519 |
| rs225145886 | in-del | -/TGGA | | | intron-variant | Eml1 | Mm_Celera | 12:108397237 | CTATTGGGTTGGGGG[-/TGGA]GGGGGCATTCCGAAT | 68519 |
| rs225158448 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453680 | CAGCCAGATGAGCTG[G/T]CTGTAAGTCCAACAC | 68519 |
| rs225160871 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108518895 | TACCGACATCACTAC[A/G]TGTCTGCGTTAGACA | 68519 |
| rs225162134 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108462825 | CCATAGCTGTCACAT[-/A]AGGATTTCTTTACCG | 68519 |
| rs225166149 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108394905 | TCCTCACAGACGAAT[C/G]TCCCCACAGGACAGA | 68519 |
| rs225195252 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526698 | GCAGCACCATGAACC[G/T]CAGGCAGCCTTGCTG | 68519 |
| rs225218128 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108492673 | GTGACAGTCACAATC[A/C]TGCCTCAGTGTTCCA | 68519 |
| rs225236514 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390345 | ATACACAAGAACATA[C/T]AGACCTTACACAAAA | 68519 |
| rs225238753 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108498474 | GTGACATTCCCTTAT[-/G]GGGCGGCCTCTGTTC | 68519 |
| rs225248901 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108374905 | ACAAACCTGACAGCT[A/G]TCTCTGCCCTGGATT | 68519 |
| rs225261378 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453297 | TGTGTACACATGTAA[G/T]TGTAGGCCAGAAATT | 68519 |
| rs225268617 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108418399 | aggctatgaagggat[A/G]ttctttactggcttg | 68519 |
| rs225287098 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108419595 | AAATTTCTGTTTCTT[C/T]TTCTTCTTCCCCTTT | 68519 |
| rs225300272 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500440 | TTATTTATAATGGAA[C/T]TATTTGCTCTTTATT | 68519 |
| rs225302611 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108391653 | CTTCCCTCTGCTTTT[C/T]CTTTCCTGATGGGGA | 68519 |
| rs225303887 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421970 | TCACCCACCTGGTAA[C/T]AGTTGAATTAGCAGC | 68519 |
| rs225314011 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468230 | GGTATGGCTGACTAA[C/G]AGTGGATAGTCTCAC | 68519 |
| rs225337474 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519448 | CATTCGACTGTGTGC[A/G]TGCGTGTGGGAGCGT | 68519 |
| rs225339710 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499921 | GAAGGGAGGGGGGAA[A/G]ATCAAACATTCACAG | 68519 |
| rs225341716 | in-del | -/TGAATGGTTTTTCCT | | | intron-variant | Eml1 | Mm_Celera | 12:108383410 | CTTTATCCTTGGACC[-/TGAATGGTTTTTCCT]TGACACAAATTTGTC | 68519 |
| rs225341957 | in-del | -/GGTCCTAGAGGT | | | intron-variant | Eml1 | Mm_Celera | 12:108535170 | TGAACCCTGTGCAGA[-/GGTCCTAGAGGT]GGGACAGTCCCACAG | 68519 |
| rs225344201 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442256 | TGAATCCAGGGTGTG[C/T]CTGCCAGCACTCACA | 68519 |
| rs225372129 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108498686 | TTAATTCTATGTGTA[C/T]GAGAATTTTGCCTGC | 68519 |
| rs225387096 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526120 | CGGTGGCAAAGACAT[C/T]ACATTCATTTTGAAC | 68519 |
| rs225387862 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108523047 | aaatctacagaactc[C/T]aaatagactggacca | 68519 |
| rs225413249 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504845 | CGAAGTATTTTTGGG[G/T]CCTAGAGAGATGGTG | 68519 |
| rs225415934 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108497417 | CCTCCAGCAGGAGAT[A/G]CTTCTGCGGCTGCTC | 68519 |
| rs225427254 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527303 | TTGTGGTTGCAGTTT[A/T]TCTAGTAGCATCTCT | 68519 |
| rs225442317 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471512 | CAGGGAGGGGGAGCA[A/G]GGGAGGAGGAGCAGG | 68519 |
| rs225443107 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108391902 | TCGGCAGTGGGGCTA[A/G]TCCAGGGTTTGGCTG | 68519 |
| rs225480584 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108523779 | AAGGACACTTCATAC[A/T]GGTTAAAAGAAAAAT | 68519 |
| rs225484339 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532306 | TCAGATCCTTTTACA[A/G]ATGGGTGTGAGCCAC | 68519 |
| rs225488714 | in-del | -/TCAACAGCAGAAGGAAGGGGA | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412197 | CGGGTGCTGAGGAGT[-/TCAACAGCAGAAGGAAGGGGA]TGTGCAGAGGAGAGG | 68519 |
| rs225498610 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108420426 | TTACTTTCTTTGAGA[-/TT]TTTTTTCTTTCTTTT | 68519 |
| rs225510167 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390754 | GACACCCCACACATG[C/T]GCACACCCAACCATA | 68519 |
| rs225514198 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504482 | TCTGAAGTGCATGCA[C/T]GTGGTGACAAATACT | 68519 |
| rs225524341 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108531882 | CTATGATGTCATTAG[C/T]ACAGTGCTATTGGCC | 68519 |
| rs225526288 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478449 | TACATTGTAGCTGTC[C/T]TCAGACACCCCAGAA | 68519 |
| rs225532161 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108392567 | TCCTTCAGCCCCCAC[A/G]GCTTCAGTTTCCCTA | 68519 |
| rs225546925 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108496424 | GCAAGGGATCATATC[A/C]CTGATACAGCGTGGG | 68519 |
| rs225550073 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108374538 | GGGTTGCTCTATCAA[G/T]GTCAGCTCCCTTCAT | 68519 |
| rs225554411 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530156 | TGTCAATATCCTGTT[C/T]CTTTCTGTAGAGAAA | 68519 |
| rs225576318 | in-del | -/GGAGGAGCTGG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471534 | AGGAGCAGGGGAGGA[-/GGAGGAGCTGG]GGAGGAGGAGCTGGG | 68519 |
| rs225592382 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442499 | AAATGTGCTTGCAGC[C/T]CTTTACACTGGAACA | 68519 |
| rs225597995 | in-del | -/ATGGCTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108382316 | TGCAAAAAGCCAGGC[-/ATGGCTGT]ATGTGCCTGTGACCC | 68519 |
| rs225612830 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108373985 | CTTCACCAAACAAAG[C/T]GTTAGTTTCATCAGT | 68519 |
| rs225616959 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108399862 | TCCCCTCTCCAACAG[A/T]CACAGCCCCAAATCC | 68519 |
| rs225617773 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108467520 | CTAGAGTCGGCACAC[A/G]CACAGCCTTCCTCTG | 68519 |
| rs225657730 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108444983 | GCATGCCTTTGTCCC[A/T]CTCTTCTCCCCCACA | 68519 |
| rs225663441 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466948 | TTGGATATCCTGAAG[C/G]TGCAGTTAACAGGCA | 68519 |
| rs225669017 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503349 | TTCTGTTATCTCTCC[G/T]AAGTTCAGTGCTCCT | 68519 |
| rs225696696 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402528 | TCACAGTCAGGCACC[A/G]CACCAAGTTTATGTG | 68519 |
| rs225700727 | snp | A/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404030 | GCGCACAGGTCAGCC[A/T]CTAATGCAGTGAGCC | 68519 |
| rs225701406 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108497052 | TGGGACATAGTGGAA[A/T]CTGTGCCTGTAACCA | 68519 |
| rs225718600 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451065 | GGACAGAGACAATGC[A/G]TTTGATTGTTTATCA | 68519 |
| rs225729973 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108372951 | TGTGTCTCAAAAACC[A/C]GAAACAACAGAAAGC | 68519 |
| rs225748884 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474413 | GTGCCTGTGGGACCT[G/T]CGGAAAGATCTCAAC | 68519 |
| rs225749229 | in-del | -/AC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108434702 | CACACACACATACAT[-/AC]ACACACACATACCAC | 68519 |
| rs225785369 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455845 | TCTGAGCCTGTCATG[-/T]TTGCTTGCTCCTGTG | 68519 |
| rs225796013 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442828 | TCTACTCGTACTTCT[C/G]CTGTGTATGATATGT | 68519 |
| rs225812801 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449117 | TTTGTTGTTGTTGTT[G/T]TTTTAAAGACAGGGT | 68519 |
| rs225835459 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108426065 | ATGTGAAGGGCAGAG[G/T]TTGGCATCTGGTGTC | 68519 |
| rs225836836 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507915 | TGGCTCATGCCGTGG[G/T]AGGGGATCTGCCTCT | 68519 |
| rs225889751 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108385501 | AGATGCAGGTTCTGT[-/G]GGGTAAGTCCTGGGT | 68519 |
| rs225893226 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507365 | GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCGA | 68519 |
| rs225908807 | snp | A/C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108397450 | CTGAAGTCAAACAAG[A/C/G]TGGCTTTCTGCCTGC | 68519 |
| rs225921688 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470928 | GAGTTCTGGCTTTGA[C/T]TTCCCCTCAGCGATA | 68519 |
| rs225954844 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108521915 | AGCTCCACTCCCAAG[A/C]GCTTTAACACACCCA | 68519 |
| rs225963867 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478081 | AGAAAAGAGACAGGA[C/T]TAGCTAATCTTGGTA | 68519 |
| rs225970931 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446354 | CAGTGAAGGACCTGG[A/T]GGGTGACAAGAGCCA | 68519 |
| rs225973852 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376863 | AGATGTCGGGTGTGG[A/T]GAGAGCAGTTACAGG | 68519 |
| rs225974262 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108382229 | ACAGTTTTCAGGGCA[A/G]GGGAGATGACTCAGT | 68519 |
| rs225978298 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108471062 | CATATCTTAAGCAGC[A/C]AAAGCATCGTTGCAT | 68519 |
| rs225996419 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108529567 | GATAAACATCACCGT[C/T]GTCGATCTGCTGACA | 68519 |
| rs226018119 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108478155 | GAACATTTCCTTCAC[A/G]CACTGTCACCATCTG | 68519 |
| rs226020623 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108452367 | TTGCACGTGGCAGCT[C/T]GCAGGGTGAGGATTA | 68519 |
| rs226035402 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421577 | CCTTCTGGGCCTGTC[C/T]TACAGTGATCTCCCC | 68519 |
| rs226038590 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108381707 | ATTAGCTGTTGATGG[G/T]CAAGAGTCTCGCTTT | 68519 |
| rs226039436 | in-del | -/CA | | | intron-variant | Eml1 | Mm_Celera | 12:108521309 | CATGTGACTTTTCCC[-/CA]CACAGATTCCTGAGC | 68519 |
| rs226076098 | in-del | -/CACACACACACACACACACACACACA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108414394 | GCGCATTCACTCGCG[-/CACACACACACACACACACACACACA]CACACACACACACAC | 68519 |
| rs226097976 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430710 | TCAGCTGTGAGATCC[C/T]ACCTTACCACCTCCA | 68519 |
| rs226102529 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477799 | TGCTGAACTTGTTTA[C/T]TTGTTGTGCCTCATC | 68519 |
| rs226108259 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108415038 | ACAATCTATTATCCT[C/T]ACTGGAATACATAAG | 68519 |
| rs226110571 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387352 | TGAGATGTAAAATGT[C/T]CCTACAGCCTCTTGT | 68519 |
| rs226128113 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108526748 | ACTCACACACCCCAC[A/C]TAAGGAAACAGCCCT | 68519 |
| rs226139592 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108419152 | TGCAAGTAGAACCTA[C/T]AGTATTTAATCCTTT | 68519 |
| rs226145729 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530991 | GATTTGTTCCTGTTA[-/T]TTTTTTTTAGTGTTC | 68519 |
| rs226153032 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430212 | GCACATTTCCTATCC[C/T]GCTGGGAGCATGGCT | 68519 |
| rs226156868 | in-del | -/CATGTATG | | | intron-variant | Eml1 | Mm_Celera | 12:108494914 | GCTCACCTGCATGGA[-/CATGTATG]CATGTATGCGAGCCA | 68519 |
| rs226170483 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108388895 | TAGCTGGCCAGAGAG[C/T]TGGTCTCTCCTCTTT | 68519 |
| rs226182461 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390752 | CAGACACCCCACACA[C/T]GCGCACACCCAACCA | 68519 |
| rs226198146 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402080 | AGCTCTGGCCAGCAT[C/T]AAACTCATGGAGATC | 68519 |
| rs226202372 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108428658 | AGATGTTGAGAAAAA[C/T]CTTGTCAGGTTCCCT | 68519 |
| rs226215903 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108451967 | CAGCTAAGCCCTACC[C/T]AGTAAAGATTCCACA | 68519 |
| rs226235621 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108524596 | AGAGCGTACACTAGC[A/C]GCTTGACAGCATACC | 68519 |
| rs226251505 | in-del | -/TCAAAGACATAAAC | | | intron-variant | Eml1 | Mm_Celera | 12:108497239 | GGGGCTGGAGGTGAG[-/TCAAAGACATAAAC]TCAGGGAGCAGGTGA | 68519 |
| rs226256284 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108451550 | CAGGAAACCTTTGGG[A/G]GTGGTTCAGATGTGC | 68519 |
| rs226267973 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108428046 | GAACAGCGTCTTCTG[A/G]TGGAGCCCAGGCTGA | 68519 |
| rs226274060 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108398317 | GTGTGTCACTGGGCC[C/G]GGCTGCCCTTTATCT | 68519 |
| rs226317909 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482877 | GATTCGTTGAAAGAG[A/G]TCACAGTTTTTAATT | 68519 |
| rs226326964 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524247 | GAGAAACCCTGTCTC[A/G]AAAAACAAACAAACG | 68519 |
| rs226328772 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108447030 | GCCAGGCATCCGGGG[A/G]GTGGCAGAGCCAGGG | 68519 |
| rs226332879 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108495137 | TCACGGGATTCAAGG[C/T]TTGGGCATCTTTTTG | 68519 |
| rs226341153 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108505485 | CCCACAAAAAACACA[A/C]AAAAAAGTCTTATTT | 68519 |
| rs226349851 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108420149 | TTGCTTTTTTTTTTT[-/A]ACCCAAATTTTATAA | 68519 |
| rs226350789 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449447 | TATATGTATTACACG[A/G]CATCAGAGTGTTCTG | 68519 |
| rs226363931 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530464 | TTGACAAAGCTCCAC[C/T]AAGGGACTTAACTTA | 68519 |
| rs226363972 | snp | G/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536703 | ATGTGGATGATGTTA[G/T]ACCCACAGGAACACA | 68519 |
| rs226418657 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477183 | AGACCAACATGATCT[A/T]CAGAGTAAGTTCCAG | 68519 |
| rs226420481 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108396475 | TACACTGATGGCCAA[C/T]GGATACCAGTGGCTG | 68519 |
| rs226471557 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403160 | CCACCCGTCCCCTCC[A/G]ACACCCAGGCTCTAG | 68519 |
| rs226481567 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433152 | CCTGGGGAGCGGGTG[A/C]GTGCGCATGGACACT | 68519 |
| rs226511767 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108529713 | CTGGCTAAGCCCAGT[A/G]CGTGTGTTATGTGCC | 68519 |
| rs226524249 | in-del | -/ACACACAT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473006 | CATACACACACATAC[-/ACACACAT]ACACACACATCAAGC | 68519 |
| rs226541923 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432792 | CAGCCATCAGCACCA[A/G]CAGTAATTACATCAC | 68519 |
| rs226560216 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108371833 | CATGGAGGTGGCTGG[A/G]GATACAGGTGGGAGG | 68519 |
| rs226575346 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454962 | GTCAGGAATGTTCCA[C/T]AGAAAGGTTGTTGAG | 68519 |
| rs226579228 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108431300 | GCAATGTAGAGTTGG[A/G]AGATGGCTCAGTGGG | 68519 |
| rs226590149 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108372195 | GGCATCTTCCCTTGG[C/T]GTCCTTAGTTAAGAC | 68519 |
| rs226611086 | in-del | -/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450263 | ACACTTCCGGGGGGT[-/G]GGGGGGTTTATCTCA | 68519 |
| rs226623423 | snp | C/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421882 | TGAGCCCCTCATTCA[C/G]GTCAGGTCAGAGCTC | 68519 |
| rs226639573 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437706 | CCAGTACCCATAGTG[A/G]CTATCTCATGAATGT | 68519 |
| rs226640932 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504218 | ATGGATGAAGAATCT[A/G]ATGAAGTGCACTGGA | 68519 |
| rs226673420 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108478361 | TTAAGAATGTTTAAA[-/AG]GATTTCTTTATTCTT | 68519 |
| rs226685490 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108511274 | TTTCCATTTTTGGCA[C/T]CCTGATTGAATCCTT | 68519 |
| rs226689430 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108472688 | TACCCCGCAGGCCAG[C/T]CAGACTAACCTTCTC | 68519 |
| rs226718392 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108533948 | CTCTGTCACCCTTAC[C/T]AAATGCCTGGTCTAG | 68519 |
| rs226747901 | in-del | -/TT | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407746 | CCCCAAGTGTTGACA[-/TT]TTTTTGTTAGTTAAC | 68519 |
| rs226769220 | in-del | -/TAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108416758 | TGACCATGGGCCTAC[-/TAAA]ATTCACCCCTTGGCT | 68519 |
| rs226771283 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507063 | GGCAGGAACTTGGAG[G/T]CAGGAGCTGATGGAG | 68519 |
| rs226774696 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108479899 | TTGCTAGAGGTGTTT[A/G]GATTTTGTTGATCTG | 68519 |
| rs226782538 | in-del | -/CCAACCTCCGGGG | | | intron-variant | Eml1 | Mm_Celera | 12:108498383 | CTGAGGCATTTTCTT[-/CCAACCTCCGGGG]CTTTGATTTCCCAGG | 68519 |
| rs226810504 | snp | A/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108479308 | AATTGAGATGGCTGT[A/G/T]TAATGTTTGCTCTTC | 68519 |
| rs226850164 | in-del | -/AC | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404683 | CATGCATGTGCAAAT[-/AC]ACACACACACGAACA | 68519 |
| rs226861737 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448950 | TGAACTGCTGGGACT[G/T]CAGACATGCACCACC | 68519 |
| rs226888462 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108484661 | GCCACAGAGCCCTTT[C/T]AGCAGCTCCCTCAGG | 68519 |
| rs226925777 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108498347 | ACAAGCTCTGCTTGC[C/T]CTAAGAAGGACTGTG | 68519 |
| rs226941568 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108424277 | CTTTGGTGGAATTTG[A/T]CTTTTTCTTTTAATG | 68519 |
| rs226942319 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445991 | CCGGCATGGAGGTTC[C/T]CAACTGTCTGTAACT | 68519 |
| rs226959596 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470230 | TGAATGTTCAGAGTT[C/T]TTACACTTTATACAA | 68519 |
| rs226963156 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494080 | CTTCAGAGTCTAGAG[G/T]GGGAGTGACAGTGTT | 68519 |
| rs226966233 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108484101 | GCGCTCCTCCCTCTA[A/T]CCCAGTGGCTCAATG | 68519 |
| rs226969990 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450538 | CCCGCAGCTCAGCTC[A/G]CTCTTCAGGTAGTGG | 68519 |
| rs226975649 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504723 | AGTAGTCAGAGTACC[C/T]CAAGTGGGTTGGGTT | 68519 |
| rs226980415 | in-del | -/TTTTGGTTT | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108411934 | GGGGAGGGGGAGTTG[-/TTTTGGTTT]GGTTTTTTTTTTTTT | 68519 |
| rs226994918 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108512739 | CCAGGCGGTGGTGGC[A/G]CACACCTTTAGTTCC | 68519 |
| rs227012493 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108432552 | TGCAGGGTGTGTGTG[G/T]GGTTCAGGAGAGACC | 68519 |
| rs227019508 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520207 | TGCTCTTGACAGAAG[C/T]GTTCTGAAAGTCTTC | 68519 |
| rs227041614 | in-del | -/AC | | | intron-variant | Eml1 | Mm_Celera | 12:108391096 | CAGACAGACAGACAG[-/AC]ACACACCCCAATGTT | 68519 |
| rs227050016 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108380718 | TTACGCTTTTGTTAT[A/C]GATGCTTTTGAGATA | 68519 |
| rs227056945 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449739 | TGTGTGTTTCGCATG[A/G]CGTGGAACATTGATG | 68519 |
| rs227057184 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477475 | GCACAAGTTACCTTT[A/G]AAGTCTTAATCAGGA | 68519 |
| rs227092774 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108456068 | AGCTGAATCTTCCTG[C/T]TGCAGGACAGCCTTG | 68519 |
| rs227111483 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374431 | GGTTGTTGGGTGACT[C/T]TGTTTCCTTCCATGT | 68519 |
| rs227114884 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380457 | CAATGTGTCCAATAA[A/G]TGAGACCATAGGCCT | 68519 |
| rs227166899 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455547 | CCCTGGCTATAGAGG[C/T]GGCCACCTCCTTTGT | 68519 |
| rs227167495 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482966 | TGTCCAGGGCCTTTT[A/T]AATGAAATTTTGGAA | 68519 |
| rs227175667 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108475415 | ATCCCTTTTCCCTCT[A/G]ACTCTGTTTTACCTC | 68519 |
| rs227211041 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108386689 | CGGCGGAATGCCGAC[A/G]GGCCTGGCTGGCACC | 68519 |
| rs227212590 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482450 | ACATACACACACACA[C/G]AGCAAAGAAGTAAAG | 68519 |
| rs227217494 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108450442 | ACTTCTAGGTGCCCT[A/G]GCTGAATATGGAAGG | 68519 |
| rs227233438 | snp | A/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108537196 | GAGCTAGAGAGAGGC[A/G]GGAGCTGGAAACGAG | 68519 |
| rs227248057 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108487902 | GCAACCCCCCCCCCC[C/G]ATTTGTGACCAGAGA | 68519 |
| rs227310783 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108401977 | ATTGGGTTGTCCTTA[G/T]CATAGTTATAAGCCA | 68519 |
| rs227326761 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108486998 | CTGAATAACCAGCAA[A/C]CAAAAATTAACCCAG | 68519 |
| rs227336370 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108453619 | CTTAGTCAGAGCTTC[A/G]TGCATGCCACTCTAC | 68519 |
| rs227339394 | in-del | -/GA | | | intron-variant | Eml1 | Mm_Celera | 12:108530179 | AGAGAAAGCTGTGGG[-/GA]GGAGGGGGTTTCTTG | 68519 |
| rs227346576 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108385643 | GTTTAGTTGGTAGAA[C/T]GCTCAGGTAGCAGAA | 68519 |
| rs227354995 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403379 | GGGATTAAAGGCGTG[C/T]GCCACCACTGCCTGT | 68519 |
| rs227372770 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108529327 | GTTTTGTCCCCTCCC[A/G]TCCCCCCCTCCCCCC | 68519 |
| rs227381543 | in-del | -/CGTGTGTGTGTGTGTGTG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433954 | CAGAGAGTGTGTGCT[-/CGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 68519 |
| rs227412823 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108452096 | TGTTTTCATTTAAAC[C/T]GTTTCGCTTCTCCTG | 68519 |
| rs227417746 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453005 | TATGTGAATTTTGTG[G/T]GTATGTATCTGTGTA | 68519 |
| rs227421777 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108502039 | TCAGCGGGTAAGACA[C/T]ATCGTGTGGCTGAGA | 68519 |
| rs227444114 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458640 | TATATGATTTGTTGT[A/G]AAATGTTAAATCTCA | 68519 |
| rs227467651 | snp | A/T | | | utr-variant-5-prime, intron-variant | Eml1 | GRCm38.p3 | 12:108422900 | TTCTGCCTGTAGATC[A/T]TAGGAGCAAGGACCA | 68519 |
| rs227488471 | in-del | -/ACAAACACCCATAGTACACCATAT | | | intron-variant | Eml1 | Mm_Celera | 12:108390979 | CAACACCATACACAC[-/ACAAACACCCATAGTACACCATAT]ACAAACACTACATAG | 68519 |
| rs227492962 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402123 | CCACCTCAAACTCAC[A/C]TGCCTCTGCCTCCCG | 68519 |
| rs227500429 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108469200 | CAGGTCACGTCACTT[A/C]GCACCCACCAAGTGG | 68519 |
| rs227505088 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508118 | GTACACATGTGAAAA[A/T]TTTTAACACTAGGTC | 68519 |
| rs227519053 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474639 | AGATGGAGAGTCATT[A/G]TAAGTAGGTCAAAGG | 68519 |
| rs227529095 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108381062 | TAGCATGGAGAAGGG[G/T]CGGGGCTCAGGGAGT | 68519 |
| rs227539914 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500331 | CTTCTGGTTTGCTGG[C/T]GACAACCTATGCTTA | 68519 |
| rs227548178 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108528430 | CAGCCTCCTCCACCG[C/T]GGGGTGGGCAGTAGA | 68519 |
| rs227564831 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475382 | TTTCAGCTCTCCATC[C/T]CTGCAGCCCCTGACA | 68519 |
| rs227583268 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108420555 | TTTGTTGAGACAGGG[-/T]TTCTCTGTGTAGCCC | 68519 |
| rs227585244 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377447 | TGCGTGTGCCCTCCC[C/T]CGCCATGTGTAGGGC | 68519 |
| rs227614650 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476654 | GCAAGGGTTCATTTC[C/T]GGATTTACACTTCTG | 68519 |
| rs227619978 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474062 | CCCAGCCCATGAAAT[A/G]GAGCTGCTCACAGTG | 68519 |
| rs227629591 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504309 | AGTGATGGCAGTCCC[A/G]GGTGAGCCGATCTGG | 68519 |
| rs227636236 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408271 | AATTTCTTAAAATTT[A/C]TTATTTCATGCATAC | 68519 |
| rs227637874 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405413 | TTGATTCAGGGCTGT[A/G]GAGCTGATGGTGCTG | 68519 |
| rs227646728 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108382290 | GACTCCAGTTTTAAT[C/G]CCCAGCACCTCTGCA | 68519 |
| rs227648701 | in-del | -/GGA | | | intron-variant | Eml1 | Mm_Celera | 12:108471527 | GGGAGGAGGAGCAGG[-/GGA]GGAGGAGGAGGAGCT | 68519 |
| rs227649632 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108528175 | ATTACAGTTATGAAG[C/T]AGCAGTGAAAATAAT | 68519 |
| rs227665456 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108511349 | TTGACCTGTGAAGAA[A/G]CCTAGAGAGACCACA | 68519 |
| rs227665607 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503847 | GGCTGGGTTGATCCC[C/T]GCATTACAGAGTTAG | 68519 |
| rs227665946 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108373784 | GGAGCACAGCGGGCG[A/G]CGCAGGCTCTGGGAT | 68519 |
| rs227666426 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506073 | TCCTCTGGAAAAGCA[A/G]TCTGTGCTCTTAACC | 68519 |
| rs227677940 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108475568 | CGTCGTGTGGGCCCT[A/G]GGGATGGCACTCTGC | 68519 |
| rs227685954 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108453816 | ACTGTAAGGACTCTA[C/T]GAGAGATGATGAAAT | 68519 |
| rs227692619 | snp | A/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407332 | GCTTTTCCTGCAGAG[A/T]GGGGAGAAAAGAGGT | 68519 |
| rs227719005 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403799 | CCCAGCAACTCCAGC[A/G]CATGATGCCCCCAAA | 68519 |
| rs227730603 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503389 | CACTTGAACGGGCTT[C/T]GACATGCGGCTGTGA | 68519 |
| rs227746106 | snp | A/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536591 | ATCTGTTCTGTTCCC[A/G]CCTGGGGCCATGATT | 68519 |
| rs227746430 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452491 | ATGTGCATAACGGGC[A/T]AAGCACAGGCCAGCG | 68519 |
| rs227769410 | snp | A/G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379678 | ATCCTTTATTATTTA[A/G/T]TTTTTTTTTTTGTGA | 68519 |
| rs227770319 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108375277 | GGGTGCAGGGCATTT[A/T]TTGTAGTTACATCAA | 68519 |
| rs227781929 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108387243 | AGGATCCAGATTGAC[A/G]TTGGCACTTGAGTTC | 68519 |
| rs227787685 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108509820 | ATGCCTATGGATCAT[A/C]GTATAGCTTAGGGAA | 68519 |
| rs227830269 | snp | G/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108538265 | GCAGACTCGAGTTCC[G/T]CTTGGTCACTGTGAT | 68519 |
| rs227859935 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108424023 | CACTTTTTTTTTTTT[-/T]GCATGTTGGGAGTTA | 68519 |
| rs227868897 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404789 | GCAAATACATACACA[C/T]GCACATGAACACACA | 68519 |
| rs227919003 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108425244 | CATTGAGAATTTCAC[-/T]AGGGGCATGGGGAAG | 68519 |
| rs227922505 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403979 | GCAATCACACTAATA[A/C]ACGGCCATTGCTTTT | 68519 |
| rs227940523 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480755 | GAAAGAAGCCAGCCA[A/G]ACTTCCTGAATGTCG | 68519 |
| rs227962942 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410361 | ACCTGGAGCCCCGAC[C/T]TGACTGGCACCCTAG | 68519 |
| rs227968474 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108428813 | TTGTAGGATGGTCTT[C/T]CCAGCTACTGGGTAT | 68519 |
| rs227978162 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108409339 | ATGAAATGCAATTCG[A/G]ACCCTCCCCACACAG | 68519 |
| rs227981486 | in-del | -/GTACTCG | | | intron-variant, frameshift-variant | Eml1, Gm33385 | Mm_Celera | 12:108401075 | ATGGGAACAGTTCCA[-/GTACTCG]GTTCTCTCTCCCAGT | 68519 |
| rs227998034 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108507317 | CCAAAACAAGCTGGG[A/G]TGGTGTCGCATGCCT | 68519 |
| rs228010514 | in-del | -/GGC | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403746 | GTTTTGTTTTGGGGG[-/GGC]AGGGTTTATCAGCCA | 68519 |
| rs228013701 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108377891 | GACACCTTGCTAGGC[G/T]CTGTATTTTTATTTT | 68519 |
| rs228024094 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108508585 | ATGTTCATACCAGAC[A/C]TGGTGTGTAGCCAGA | 68519 |
| rs228027150 | in-del | -/AGACAGAC | | | intron-variant | Eml1 | Mm_Celera | 12:108459726 | AAAACATAGATAGAT[-/AGACAGAC]AGACAGACAGACAGA | 68519 |
| rs228030418 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108515307 | GAAATGAGCTGTTGG[A/G]GTTACGAACAGGACA | 68519 |
| rs228032787 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108507497 | AGGACTCTAATGATC[A/T]TAATTTCAACAAACC | 68519 |
| rs228037296 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108416746 | ATAGGTTTATGATTG[A/G]CCATGGGCCTACATT | 68519 |
| rs228043547 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108394566 | AGAGAGAATAAGCCC[-/TT]TCTCTGGCCCCTTTT | 68519 |
| rs228045560 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108427752 | CAATTTGCAGGGCAA[A/G]GTGGGGCGTGCTTTT | 68519 |
| rs228077106 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480036 | TCAACCCTCAGTTTT[C/G]AGTGTTTCTTTTCTG | 68519 |
| rs228089421 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108508194 | GCCCTGCGTTCAGTT[C/T]CCAGGATCCACTTGA | 68519 |
| rs228092109 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383455 | CCAAGCCTATATCTC[C/T]TTTTAGTGTAATTAC | 68519 |
| rs228116121 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108454998 | CTGACTCTCCTGCTC[A/G]GGCTTATGGTAGAGA | 68519 |
| rs228137464 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454320 | ACTATGTATGAGAAT[A/T]CAGATCCACATCTGT | 68519 |
| rs228138568 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108461365 | AAATTCGAATTAACT[C/T]TGATATTCTGTTAAT | 68519 |
| rs228143705 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433698 | GAAGATCTAATGGGG[A/G]CTCGGCCGGCTGGGG | 68519 |
| rs228144770 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377581 | AGGACTTCCTGCTTA[C/T]GGGAAGAATCCCAGG | 68519 |
| rs228145711 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108514336 | GTTAAGCATCCTAAG[A/G]GGCCTGCGGCATTTG | 68519 |
| rs228187361 | in-del | -/TTTT | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108369662 | GGGGCCCAGAACTAG[-/TTTT]TTTTTTTTTTCCTTT | 68519 |
| rs228187678 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460513 | AGAACACCAGGGGCA[A/G]GAAAATTGGGCCTGG | 68519 |
| rs228199984 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478708 | GTGCGCCACCACGCC[C/G]GGCTTCTGGCTTTTG | 68519 |
| rs228208015 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525585 | AAAGAATATAACAAA[-/T]TTTTTATATATTATT | 68519 |
| rs228212681 | in-del | -/GTAC | | | intron-variant | Eml1 | Mm_Celera | 12:108487534 | ACAGTGTGTGTGTGT[-/GTAC]GTGTACATATACATA | 68519 |
| rs228215062 | in-del | -/TAA | | | intron-variant | Eml1 | Mm_Celera | 12:108488800 | GAATTTATCTTTGCT[-/TAA]GGAATGCTTAAAGCT | 68519 |
| rs228257036 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108381166 | GCAGGGAGAGGGGCG[G/T]GGCACAGGGAGCTGG | 68519 |
| rs228260595 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387945 | ATGTCTGCTGAATGT[C/T]TCTGTGCCAGCCTTT | 68519 |
| rs228266729 | in-del | -/CCCTCC | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408537 | AAATGATGCCCCTCT[-/CCCTCC]CCCTCCCCCTCCCCC | 68519 |
| rs228276912 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108510515 | GTTCAGGAGGCAGAG[A/G]CAGGCAGGTCTGTGG | 68519 |
| rs228281885 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108429249 | CCTTCCACTGTGTGG[A/G]TTCAGGGAACTGAGC | 68519 |
| rs228300102 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532168 | AGCTATGCTTTGTGG[A/G]TGGTATTTGTGTGAA | 68519 |
| rs228306876 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520879 | AGAGGTCCTAGGTTC[C/T]ACCCCTAGCACTACT | 68519 |
| rs228309554 | in-del | -/GCACAGGGCA | | | intron-variant | Eml1 | Mm_Celera | 12:108515618 | CGCCAATACAGATGC[-/GCACAGGGCA]GCTCAGAGGCTGACG | 68519 |
| rs228317510 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108484627 | GGGCACTGCAGAATG[A/T]CACTCTGGGCCTCCC | 68519 |
| rs228327968 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108373068 | AGCCTGCAGCGGAGG[A/G]GACTCTCTGTTCAGA | 68519 |
| rs228340232 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387377 | TCTTGTGTCTGAACA[C/T]TTTGTCTGCAGATGA | 68519 |
| rs228347305 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108458028 | CACATTGCTACTTGG[A/G]ATGAGATCTTTTCTC | 68519 |
| rs228367897 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108457089 | AAGTCTCCTGAGTCC[C/G]TGACTCATTCCTCAA | 68519 |
| rs228414321 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108463059 | TGCAAGATGGATTCA[G/T]ACCGACCTGCTGTGG | 68519 |
| rs228420077 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381105 | GGGGCGGGGTTCGGG[C/G]TTCAGGGCGGAGCTC | 68519 |
| rs228434749 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379213 | TGGGTACAGATCATG[C/T]GTGTTTATGCATAAG | 68519 |
| rs228438908 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108483978 | AAAATAAATAAATCC[A/C]AAACCCACGATGCTT | 68519 |
| rs228456791 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108432177 | CCCACTCACTGCCCG[A/C]CAGTGGGCAGGAGGC | 68519 |
| rs228464410 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429208 | TGGATGGAGACTAGC[G/T]GACAGCTTGCAGAGA | 68519 |
| rs228491084 | snp | A/C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108438971 | CATCTTTTATTTTGG[A/C/G]GGACTTCTCTCTCTT | 68519 |
| rs228495653 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108390494 | aaaaattaaaaaata[A/C]ACATTTTCAAACAGT | 68519 |
| rs228505220 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473755 | CTGCCCACCAGGTGA[A/G]ACACAGAGCAGACTT | 68519 |
| rs228509236 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387326 | AAGAAGAGGCTGATG[C/T]CTGCTATGTCTGAGA | 68519 |
| rs228516703 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108497163 | AGATTCTGTCTCAGG[-/A]AAAAAATACAAAAAG | 68519 |
| rs228518369 | in-del | -/CCT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474146 | TGCCCGCAGGCGATC[-/CCT]CATCAGACTGTCTTC | 68519 |
| rs228538280 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108438305 | GCTAAGCCGTGTTCT[C/T]AGCACACAGACAGTA | 68519 |
| rs228542219 | in-del | -/TGTGTGTGTGTGTGTGTA | | | intron-variant | Eml1 | Mm_Celera | 12:108425727 | ACACGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGTA]TGTGTGTGTATTCGC | 68519 |
| rs228554028 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438297 | AAGTGCAGGCTAAGC[C/T]GTGTTCTCAGCACAC | 68519 |
| rs228558468 | in-del | -/GAAGGGT | | | intron-variant | Eml1 | Mm_Celera | 12:108497876 | ATTAAAGGGTCACAG[-/GAAGGGT]CATCAGGAAGGTCGA | 68519 |
| rs228560383 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108516177 | AACTTACCCAGGGAC[G/T]TGGCCCACTGGGGAG | 68519 |
| rs228562785 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108435638 | TTAGAAAGCTTTAGC[A/G]TCCTGGGCTCTGTAG | 68519 |
| rs228569221 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377985 | ATGCTTCCACATGTG[C/T]ATACCTATGGTCAGG | 68519 |
| rs228592526 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383614 | GGGTATCAGATCCCA[C/T]TGCAGATGGTTGTCA | 68519 |
| rs228614050 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108478882 | CTTTTCCCACTCTTG[A/G]AGAGAACGCTTACAG | 68519 |
| rs228624563 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108533025 | ATTCCGTGTGACACT[-/G]GTGGGTTTTCATACT | 68519 |
| rs228634149 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108382374 | CATGGGAGCTGGCAC[A/G]GTGATCAGCCTAGCA | 68519 |
| rs228657839 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108534128 | TCTCCATTCTGCAAG[A/G]CTAGAGAGAGGGATG | 68519 |
| rs228672723 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108531574 | CTGAGTTTGAGGCCA[A/G]TCGGGTCTACAAAGT | 68519 |
| rs228695253 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108388840 | ATCCACTGAAGCAGG[C/G]TATACCATAAGAACA | 68519 |
| rs228703235 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486149 | ACTGCTGCCTCATTA[C/G]GTATCCATTTGTATC | 68519 |
| rs228713677 | snp | A/G | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108538234 | AGTCATTTAGTCCCT[A/G]TGGGAGCCCGAGGAC | 68519 |
| rs228716981 | in-del | -/AAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108506356 | AATAAATGCATCTTT[-/AAAA]AAAAAAAAATGTAAG | 68519 |
| rs228717346 | snp | C/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536508 | TGGCACTAGAGTTAC[C/T]CATAGTTGTGAGCTG | 68519 |
| rs228725231 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440131 | CACAGTCTAAAGAGT[C/T]CTGAGGGGATGGTGG | 68519 |
| rs228738953 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108485193 | GGTAATCGACAGGAG[C/T]CCAGCGGGGACTGCG | 68519 |
| rs228751673 | in-del | -/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407486 | ATAGAGAGAGTCAAA[-/T]AAGATACAGAAAGAC | 68519 |
| rs228842313 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108506192 | AGGGACCAGAGACAT[A/G]GCTCAGCAGGTAAAG | 68519 |
| rs228844614 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478255 | CTGTGACAAACAACA[C/T]GCGTTCACCCAGGAC | 68519 |
| rs228854987 | snp | A/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410109 | TGTAGAAGTCAGAGG[A/T]CAACTTGTGGGAGTC | 68519 |
| rs228905284 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108519013 | TTTCTTTTCCCTTTG[C/T]ACCCCAATGTGTACC | 68519 |
| rs228933274 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108529888 | TGCATCTGTCATCCA[A/G]GTCTGAGATTACAGT | 68519 |
| rs228942372 | in-del | -/TT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108435125 | AACTGATATCACATA[-/TT]TTTTTTCTTATTGCT | 68519 |
| rs228945265 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108447116 | ATTGCCCAACCACTT[-/A]AGCATCAGCTGTCCT | 68519 |
| rs228958248 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437132 | ATGCTGTTGAGATGG[C/T]GAACTGGCTTATTTT | 68519 |
| rs228971755 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485179 | AGGAGGAAAAGATGG[A/G]TAATCGACAGGAGCC | 68519 |
| rs228976387 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108431088 | GGTCCCTAAGGATGC[G/T]GACTGTATTGGGGTA | 68519 |
| rs228992179 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108392723 | TGCCTCTAGGCCTTC[A/C]CTGCATTGCAGGAGA | 68519 |
| rs229012760 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108380767 | TGCCCAGAATGATGA[G/T]TACATTGGTAGATGA | 68519 |
| rs229017403 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442618 | TGGTCAGGAGCCCCC[A/C]TGTGGGTGCTGGGAA | 68519 |
| rs229017432 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436435 | TGCAGTTTCACCTCT[A/G]GATTCTGAGTGCTAA | 68519 |
| rs229051543 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108392023 | TCTGTGTTCAACATC[C/G]TCTCCCTGGGCTTCA | 68519 |
| rs229063421 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108490076 | ACCAGATCTGTCTTA[C/T]CCTTTAAATCCCATG | 68519 |
| rs229074382 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442331 | CACGGGCGTGTCTGC[C/T]GTGTGCATGGCCTCC | 68519 |
| rs229093682 | in-del | -/AAAAAAAAAAAAAAAAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108535528 | CCCTTTGTATCGATT[-/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 68519 |
| rs229095353 | snp | C/T | | | downstream-variant-500B, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108539906 | CAACTTGCATAGTGG[C/T]TCATTTGGCGTCATC | 68519 |
| rs229097475 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488932 | TCCATTCAGGTTTCC[C/T]GTCCTATACTTAACT | 68519 |
| rs229101953 | in-del | -/TGTGTA | | | intron-variant | Eml1 | Mm_Celera | 12:108519739 | GTCAGGTTCTCTCTG[-/TGTGTA]TGTGTAGCCCTGGCT | 68519 |
| rs229105876 | in-del | -/TGG | | | intron-variant | Eml1 | Mm_Celera | 12:108379509 | ATTTCTGCATTGCTC[-/TGG]TGGTGATCTCTGGTG | 68519 |
| rs229115123 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437756 | GCATCTCCCCGAGTT[C/G]TGTGCGCCGAGAACA | 68519 |
| rs229158943 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380794 | ATGAATGGATAAAGA[-/G]GGGTGGGCTATTATG | 68519 |
| rs229172148 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496726 | CCCAGCTCCCTGTGG[A/G]TGGGGCCACCTCTGG | 68519 |
| rs229186997 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108533561 | TACCATTTCCTGAGC[C/T]ATACCACCCTGTGCA | 68519 |
| rs229209808 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108490983 | ATTGACAACTTCTGG[A/T]GACTCTGAAGTGACT | 68519 |
| rs229229881 | snp | A/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379189 | tgtgtgtgtgtgtgt[A/G/T]tgtgtatgtgGGTAC | 68519 |
| rs229235135 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460472 | TAATACTAGATGTTA[C/G]GGACACATTAACATT | 68519 |
| rs229272157 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108443753 | GCTGTGCCAGAGGAT[A/G]TGCCTCAGTTCCCTG | 68519 |
| rs229299477 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108457001 | GCTTCCTCTCGGGAA[G/T]TGTCCAACCCAGAAG | 68519 |
| rs229329140 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108443307 | TTAGAACAGCCAGGT[A/G]CCTAGAAAGCTAAGC | 68519 |
| rs229345203 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408219 | CTTCCTGAGTGCTGG[A/G]ATTAGGTGTGTGCCG | 68519 |
| rs229358084 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432845 | GGAGTGCCCTTTCTC[A/G]GTGACAGAAGCCTGC | 68519 |
| rs229368567 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471138 | CCCCGGGTTTGATCC[-/G]GCACGCAATGCTGTG | 68519 |
| rs229391698 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477888 | ACACAGACGCAGAAA[A/G]GCTGGGGTCAGGTGG | 68519 |
| rs229399824 | in-del | -/CGCACACACACACACACACA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108414393 | GAGCGCATTCACTCG[-/CGCACACACACACACACACA]CACACACACACACAC | 68519 |
| rs229400144 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407230 | TTGATACAATAGCTA[C/T]TTTAAAGTTTTTGTC | 68519 |
| rs229438853 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108439406 | TACTGCCTCTGCTTC[C/T]CAACTAGTCCATAGC | 68519 |
| rs229445326 | in-del | -/GTGTGTGTGTGTGTGC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377930 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGC]GCGCGCGCGCGCGTG | 68519 |
| rs229445657 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108384718 | GTCAGGAGAGTGTCT[A/G]TGGTGCAAGCATGGG | 68519 |
| rs229448235 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376285 | CTCCTCCTCCTCCTC[C/T]GCTTCTTCCTTCTCC | 68519 |
| rs229460500 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108434812 | TATATACATGCATAC[A/T]CACACCATGTAGTAC | 68519 |
| rs229468138 | in-del | -/TTC | | | intron-variant | Eml1 | Mm_Celera | 12:108430327 | ATTTGTTTTTTTTTT[-/TTC]CCTAAGAGCATAGCA | 68519 |
| rs229478132 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108461964 | GAGCTGGAATTTTAA[A/C]ACCAATGGTTTGACT | 68519 |
| rs229490644 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108435883 | GTTACCACTTCCAAC[G/T]TGTTCTATTAACCTT | 68519 |
| rs229503319 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484688 | CAGGAGCTTCCAAGT[C/T]TGCGCTGGGTACTTG | 68519 |
| rs229503822 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108512591 | GCCTTCCAAAGGACT[C/G]GGGATCGATTCCCAG | 68519 |
| rs229541750 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108481202 | AGAGCAGGACAATTG[A/G]GTGGGAGTAGGGGTA | 68519 |
| rs229543765 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535225 | AGGTACCCACCTCAA[A/G]CAGGCAGAGACCCTC | 68519 |
| rs229553394 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108461558 | ACTCAAGCAGGTCAT[A/G]AAGCAGGAGCTGATG | 68519 |
| rs229554889 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468997 | GAATCCCAGAGAAGG[A/G]TGTGACAGTCAGGAT | 68519 |
| rs229582119 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441918 | ATTTTAGAGCCCAGT[A/G]GCTTAGGGAAGACTA | 68519 |
| rs229583850 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519532 | GCATCTCACCAAGGC[A/G]TGGAGCTTGCTTATT | 68519 |
| rs229583853 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108511613 | AAAGTTTAAAACTTG[A/T]GAGCCTTCTCCCGAC | 68519 |
| rs229586125 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108467562 | CCTTCAGGATTGAGG[A/G]CTGGGGAAGGAAAGA | 68519 |
| rs229608936 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108487972 | TAACCCCTGACTCAA[G/T]GCCACACATCTAGAT | 68519 |
| rs229627194 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523534 | TCTTTTAACATCAAT[A/G]GACTCAATTCCCCCA | 68519 |
| rs229627922 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108401599 | GGCCCAAGATTAGGT[A/G]TGCCTCCTCACAGAC | 68519 |
| rs229688329 | in-del | -/AGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108378622 | GTGGGTGTCTGAGTG[-/AGT]AGTAGTAGTAGTAGT | 68519 |
| rs229695525 | snp | C/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538389 | AAGCGGTTGTGTGTC[C/T]GCTTTTGTTATATAG | 68519 |
| rs229704637 | in-del | -/GGCA | | | intron-variant | Eml1 | Mm_Celera | 12:108512353 | CTCTGTTTAAGCCAG[-/GGCA]GGCAGTTGGCTAGAA | 68519 |
| rs229731959 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108445682 | AGTCTTCAAGGCAAA[A/G]TTTCAGATGTTCTGG | 68519 |
| rs229732006 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108439867 | TAATAATAAATAAAT[C/T]TTAAAAAAAAAAAAG | 68519 |
| rs229750216 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108493584 | CCAATTCAGACAGTT[A/C]CTCAGGGAGATGGTC | 68519 |
| rs229750696 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108497435 | CTGCGGCTGCTCCAG[-/C]CCCAGCGTTTACATA | 68519 |
| rs229770070 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108444873 | ACAGACCATCTGGCC[C/T]TTGGACAGGCCATAC | 68519 |
| rs229780157 | in-del | -/GTG | | | intron-variant | Eml1 | Mm_Celera | 12:108455267 | GCACTAGGTGTCAGC[-/GTG]GTGGTGACAAATGTG | 68519 |
| rs229782467 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108481780 | TTCTCAGAGAAGGAG[A/G]AGCCCAACATGATCC | 68519 |
| rs229816554 | in-del | -/CCTGAAG | | | intron-variant | Eml1 | Mm_Celera | 12:108535833 | AAACAGACAGATCAC[-/CCTGAAG]CCTTGGCACTTGCTG | 68519 |
| rs229842971 | in-del | -/ATAA | | | intron-variant | Eml1 | Mm_Celera | 12:108518635 | CCATGTCTTCCAGAC[-/ATAA]ATAAGACTTTTATGT | 68519 |
| rs229847917 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442280 | ACTCACAGATGTGTA[A/G]CGCACAGCTCCACTG | 68519 |
| rs229860267 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492920 | CCACTTTGTGTTCCA[C/T]GATTTTAAATCACTA | 68519 |
| rs229866081 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108501226 | TTCTGTTGATGGACA[C/T]ATAGCTGATCCCATT | 68519 |
| rs229869641 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108434230 | TTCTGGCTCCAGTGC[C/T]TGGGCCATACTGAAT | 68519 |
| rs229872730 | in-del | -/A | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474350 | TCAAAAAACAAAAAC[-/A]AAAAAACCTCACCAT | 68519 |
| rs229903336 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488851 | TGGATAGGTTGAAAG[C/G]TGTGCTTTTGAACTC | 68519 |
| rs229905318 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494149 | GAGCCCCTTTTTTAG[A/C]CCCCACCTGAGGTAG | 68519 |
| rs229932239 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108412085 | GCAATCCGACTGGGA[C/T]CAGTCTCTAACTCCC | 68519 |
| rs229936055 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108535394 | GTCGTGGGGGGGGGG[-/A]GGAGTGGGATGTGAG | 68519 |
| rs229941201 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108495081 | AGACACCTCCCCAGC[A/G]CCTGAAACTGCATTT | 68519 |
| rs229949924 | snp | A/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412679 | CATGTGAAGCTGGGC[A/G]TAATGGCTCACACCT | 68519 |
| rs229952273 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369267 | CCCTGAGATGCCTCA[A/G]GACAGTAAGAGGAGG | 68519 |
| rs229972024 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108494263 | TCTAAGAGAGCAGGG[A/T]CACTGTCCTTTCTTA | 68519 |
| rs230006332 | in-del | -/CT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376282 | CTCCTCCTCCTCCTC[-/CT]CCGCTTCTTCCTTCT | 68519 |
| rs230016634 | in-del | -/AAATTAAAAAATAC | | | intron-variant | Eml1 | Mm_Celera | 12:108390481 | GTAATAATAATAAAA[-/AAATTAAAAAATAC]ACATTTTCAAACAGT | 68519 |
| rs230025232 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372289 | TCACAGGCATGCCAG[A/G]CTGTCCCGGGAGGCC | 68519 |
| rs230026142 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447003 | ATAGGCAAGGCTTAC[G/T]GCTCCAGTAAGGCCA | 68519 |
| rs230042187 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429246 | TCTCCTTCCACTGTG[-/T]GGGTTCAGGGAACTG | 68519 |
| rs230047515 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406974 | TAATGCTTCAACTTT[G/T]CCCGTGTTGTGGCTT | 68519 |
| rs230059247 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404808 | CATGAACACACACAC[A/G]TGCAAGTGCAAATAC | 68519 |
| rs230062225 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455480 | TGTAAAACTACCATT[A/T]AGGAGACTATGGTGG | 68519 |
| rs230063782 | in-del | -/ACACAT | | | intron-variant | Eml1 | Mm_Celera | 12:108485489 | CACCCACTCATTCAC[-/ACACAT]ACATACACACACACA | 68519 |
| rs230065003 | snp | A/C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446262 | ATAAGGTCATTAATA[A/C/T]GTCAGGGCACACCCT | 68519 |
| rs230073538 | in-del | -/CG | | | intron-variant | Eml1 | Mm_Celera | 12:108387650 | AAACAAATCCTTCTC[-/CG]CCCCCTCCAGCTGCT | 68519 |
| rs230073700 | in-del | -/TC | | | intron-variant | Eml1 | Mm_Celera | 12:108439372 | AGATGCCAGGGCTGG[-/TC]TTGAACTTGCAACCT | 68519 |
| rs230079586 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108371825 | CTGGGCTGCATGGAG[A/G]TGGCTGGGGATACAG | 68519 |
| rs230132942 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412910 | TATAGTTTATGTATG[C/T]ATTCTTCCAACTGAA | 68519 |
| rs230149931 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419195 | GTCACTCAGCATAAT[A/G]TTCTCAAAGTTCAAC | 68519 |
| rs230154869 | snp | A/T | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411542 | TAGTGGCTCAGCTGC[A/T]CCCCTGAGAGACTCT | 68519 |
| rs230173990 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108460020 | TGCTGCTTGTGAGGA[C/T]ACCAGTCTTGTCAAC | 68519 |
| rs230181019 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108472044 | CTTCTCAAAGCAGCT[C/T]TTTGGGGGTCTAAAA | 68519 |
| rs230212325 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418239 | CTGTCTTAGTCAGGG[A/T]TTCTATTCCTGAACA | 68519 |
| rs230251011 | snp | A/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471449 | AGAAAGAGCAGGGAG[A/G/T]GGGAGCAGGGGAGGG | 68519 |
| rs230262896 | in-del | -/AGA | | | intron-variant | Eml1 | Mm_Celera | 12:108471255 | GGACAGGGGAGGAAG[-/AGA]AGGAGAAAGAACAGG | 68519 |
| rs230275965 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417732 | GAACAGACAGTTGCA[C/T]TGTCAGGCAGGCAGG | 68519 |
| rs230282424 | snp | A/G | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | GRCm38.p3 | 12:108400697 | AACCGTCATAGTCTC[A/G]GGAAGGTTGAGAACC | 68519 |
| rs230296397 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499225 | TACTCACTCACACAC[A/C]CCCACCCACACACAC | 68519 |
| rs230326090 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524300 | AAAACAGGCCTCAAG[A/G]GATACAAGAAGAATG | 68519 |
| rs230335133 | in-del | -/TG | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411214 | GCCTTCATCGCTGTC[-/TG]TATTCCTCACCAGGT | 68519 |
| rs230365423 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108389501 | ATTAAGTGTTACAAA[C/T]GACTTGGAAATGACT | 68519 |
| rs230377765 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406144 | TCCCCCACAACTTTT[C/T]TTTCTCCCACTCCCC | 68519 |
| rs230387886 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473365 | acccatacacacaca[C/T]acacacaccacaAAG | 68519 |
| rs230419380 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455071 | GTGTGCATGTGTGTG[C/T]ATGTGTGTGTGTGCG | 68519 |
| rs230431035 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108374850 | ACTCCTCAAATCCAC[A/G]CTGCCCAAGACTCCA | 68519 |
| rs230444552 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108448897 | ATCATCTTAGAGCCA[A/G]GGATGGCCTTGATCT | 68519 |
| rs230457173 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108415359 | TTCTCAATGTGATGG[C/T]ATAGTTAAAAAAAAA | 68519 |
| rs230467854 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108468030 | TCTACCAACAGACAG[C/T]CCAAGAATGTAGAAG | 68519 |
| rs230484315 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374347 | TTAGAGAGCATGTGG[G/T]GGGGGACTCTGTTTG | 68519 |
| rs230514615 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108414642 | CTTGTGAAGCCCCAG[C/T]GTAGTGAGAGACCCT | 68519 |
| rs230547538 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467227 | CTCTTCTTTATAATC[A/G]AAGTCACCTCTGCGT | 68519 |
| rs230566632 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108494677 | GAACACAGACACTCC[-/A]AGTAGCCCTTGATGC | 68519 |
| rs230571912 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108421840 | CCTTTCCCTCAGCCC[A/G]ATCTCTTTCCCCACA | 68519 |
| rs230578784 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474831 | GGTGATGGTGGCACC[A/C]GCCTTTAATCCCAGC | 68519 |
| rs230591380 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518963 | GGGCACATTCTTAGG[C/T]CCTTTCCCTTGGAAT | 68519 |
| rs230607409 | in-del | -/AT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451288 | CACAATCATGAGTGC[-/AT]ACGCGCACACACACA | 68519 |
| rs230625163 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108425426 | TTCAGGAGAGGCAGC[A/G]CACAGCGAATGGATG | 68519 |
| rs230626449 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421399 | TGCTCTTTCCAAATT[C/T]TCTGCCTTGCCATCG | 68519 |
| rs230634811 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519221 | ACAGTTTGCTTAGCG[A/T]TTGGGGGAATGTGCC | 68519 |
| rs230661262 | in-del | -/AACACAC | | | intron-variant | Eml1 | Mm_Celera | 12:108390047 | CCCTTAAAAAAAAAA[-/AACACAC]ACACACATTGTAGGA | 68519 |
| rs230681419 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527118 | CCTTAGCCTCTCCAC[A/G]CCTCCATATGAAAGC | 68519 |
| rs230681576 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108518831 | GCTGGGATTAAAGGC[A/G]TTCACCACCACTGCT | 68519 |
| rs230719385 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108463402 | GAACCGTCTCACGTG[A/G]TTCTGCCAACAAACC | 68519 |
| rs230732621 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445396 | CCTGTGAGCTCCAGC[A/G]TCTTCGTCCTTGGGG | 68519 |
| rs230742229 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108515413 | GGAATGTTAAGAGTC[A/G]CTAACTTTGTGTATA | 68519 |
| rs230773914 | snp | A/G | | | intron-variant, missense | Eml1, Gm33385 | Mm_Celera | 12:108411023 | TGGAGACAAGGAAGG[A/G]CTTGGTCAGAAGAGC | 68519 |
| rs230776445 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108493394 | TTCAACACTCTCTTG[G/T]CCTCTGTGGGCCACA | 68519 |
| rs230802415 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108462782 | AGGTGTCCAGGGCTG[A/G]GAACTGTGCCTCTGG | 68519 |
| rs230815195 | in-del | -/TTTGTTTG | | | intron-variant | Eml1 | Mm_Celera | 12:108428867 | GAAATTTGTTTTTTA[-/TTTGTTTG]TTTGTTTGTTTGTTT | 68519 |
| rs230821985 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522021 | GGCACCCAGGAACTC[C/T]GCCTGACCAGTGGCA | 68519 |
| rs230837016 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470216 | TGTTTTCTTACTGTT[G/T]AATGTTCAGAGTTCT | 68519 |
| rs230842220 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520997 | ATCACTGCTCAGCAG[C/T]TGGTTCTGGTATCTG | 68519 |
| rs230903045 | in-del | -/TTC | | | intron-variant | Eml1 | Mm_Celera | 12:108383486 | GAAAGATTATTCTAT[-/TTC]TTATTATGCAGCCTT | 68519 |
| rs230909191 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108387607 | TCCCCTCTATTGTGG[A/G]CTGTACCCTCCCATC | 68519 |
| rs230914111 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108388131 | GAAGGCCGGGTCTGA[A/C]GTTAGTGTCCCAGGG | 68519 |
| rs230927555 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108508689 | GATCACCTGCCTCAA[A/G]CACAGCCTGAGAGCA | 68519 |
| rs230971002 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108430302 | CAAATGATTTTTGGG[A/G]GGAGACTTTTATTTG | 68519 |
| rs230976502 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443860 | TCCGTCTGGTGGCCG[C/T]GACTCAGGAGGGTTA | 68519 |
| rs230986356 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108465051 | GTTTCTTTGAGATAG[C/G]GTTTCTCTGTGTAGC | 68519 |
| rs231006969 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108416786 | GCTATATCATCATCA[C/T]CACCACCACCATCAA | 68519 |
| rs231010098 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108528057 | CTAGAAACGCTCCCA[A/G]AATTCTGCTCTAGAG | 68519 |
| rs231014627 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108516804 | CACTTCCTGTTTGGA[A/G]CATTGCTTTAATATA | 68519 |
| rs231019153 | snp | G/T | | | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108422599 | TCCTTGGTCCCCTCT[G/T]GGGGTAGGGACATGG | 68519 |
| rs231019565 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108431307 | AGAGTTGGGAGATGG[C/T]TCAGTGGGTAAAGTG | 68519 |
| rs231025230 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443528 | TGGCTCAGAGTCCCA[C/T]CACCAAATTCCTGCA | 68519 |
| rs231049477 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108463101 | TGAGTGGCTACAGGC[G/T]TAGCACACCAATGGG | 68519 |
| rs231049547 | in-del | -/GAAGTTTATAGCTGGT | | | intron-variant | Eml1 | Mm_Celera | 12:108450326 | AGAATTGCCACTCAG[-/GAAGTTTATAGCTGGT]GACTCGTGTGGCACA | 68519 |
| rs231064503 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108393658 | GAACAACACCCCCGA[A/T]GCCATCAGGGCCTGG | 68519 |
| rs231073596 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108514591 | AGCGCTGAGATACTT[A/C]AGTCTTAGTGATTGT | 68519 |
| rs231089528 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492223 | TGTACAGCCCTGTTG[C/T]TTCGCAGCCTGTCCA | 68519 |
| rs231092284 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470533 | AACTGGAGTTGTGGA[C/T]AGTTGTGAGCCACTG | 68519 |
| rs231103124 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108535580 | AACCTTATGAATAGA[-/A]AGTTCAGATGCCAGT | 68519 |
| rs231112592 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108383838 | TAATTCATCTAAACA[A/G]CATTAATTCATGAAA | 68519 |
| rs231125901 | in-del | -/GGGCTCTGGA | | | intron-variant | Eml1 | Mm_Celera | 12:108371951 | TCAGTGTTTACCATG[-/GGGCTCTGGA]GGAAGTGGTCCAGGC | 68519 |
| rs231129647 | in-del | -/ACACAA | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404974 | GTGCACGCGTACAAC[-/ACACAA]ACACAAACTTCTACA | 68519 |
| rs231131813 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378585 | GGCCAAAGCATGTCA[C/T]ATGACGTACATGAAG | 68519 |
| rs231159988 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108373607 | CTGGGTCTGTCTTTG[-/T]ACCCAGGTTAGGTCC | 68519 |
| rs231193038 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473454 | TTGGATATGGGGACT[A/G]CACCTGCTGCCTCTG | 68519 |
| rs231197219 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108440833 | GCTTGGCCAGCGCAG[A/G]GCCAGTCTTCTTTTC | 68519 |
| rs231212662 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108517432 | CTGTGCACACTCATG[A/C]ACATACTTGTGGAGG | 68519 |
| rs231224843 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419380 | TGTGATATACATGAC[A/G]CTGGCATGTGTGTGG | 68519 |
| rs231227279 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108480280 | CTTGCTCTGTAGACT[A/G]GATCCTTTCTCTCTC | 68519 |
| rs231233196 | in-del | -/GGCTTGGAAC | | | intron-variant | Eml1 | Mm_Celera | 12:108381810 | CAGTGCGGCGCGTGA[-/GGCTTGGAAC]AGATCAAGGGGTGTC | 68519 |
| rs231237018 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108486205 | GACTAATGAGCTAAG[A/T]CCCCAAGGTTGACCT | 68519 |
| rs231250507 | in-del | -/CT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108505070 | ATTCAATCTAGAAAA[-/CT]CTGCCTCCCCGTCTC | 68519 |
| rs231253300 | snp | C/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536549 | GCCGGGACTCGAACC[C/T]TGTTCCCACCACTTT | 68519 |
| rs231268200 | in-del | -/AAC | | | intron-variant | Eml1 | Mm_Celera | 12:108499010 | AATAAATCTTAAAAA[-/AAC]AAAAAAGAAGAGATG | 68519 |
| rs231271629 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108493831 | TTCACCTTCGCGGGA[C/T]TTGTTGACAGCACGG | 68519 |
| rs231292194 | in-del | -/GCTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108530568 | ACAAATCCCCCGCCC[-/GCTGT]CTAGTCCTCTCTGTT | 68519 |
| rs231307969 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479562 | CTCTGTCCCCTTCAG[C/T]TCCAAAGAGGAGAAT | 68519 |
| rs231318159 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446871 | GTGAACTGCACCCCC[C/T]GTGCAGAAGGGCTAG | 68519 |
| rs231333136 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525752 | TTCGAGGCTAGCCTG[G/T]CTAACAAAGTAAGTT | 68519 |
| rs231354949 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108384312 | GAGGTACCCCCAAAG[C/T]TCCAGCCATCTGATA | 68519 |
| rs231356990 | in-del | -/CAGGCACCAGTGCTCTGCAC | | | intron-variant | Eml1 | Mm_Celera | 12:108486388 | TGAGTGAGAGTCCAT[-/CAGGCACCAGTGCTCTGCAC]CAGTGGCAGCCTGGT | 68519 |
| rs231385452 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108525060 | TCTCTTCTAGAAACA[C/G]TGATAATCTTTTTTG | 68519 |
| rs231396131 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108394215 | CCCTTGGAATTCAAG[A/G]CTGGCATGGGCAACA | 68519 |
| rs231410549 | in-del | -/CCCCG | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408721 | GGCCACGCCACCCCC[-/CCCCG]AGAAGATGGTGCTTT | 68519 |
| rs231421680 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108386593 | AAGGTGCTGATGGAT[A/G]TGGCCCAGCCCCGGG | 68519 |
| rs231424060 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452264 | TGGTGTGTGGTTCTT[C/G]CTCATAGTGCCTATG | 68519 |
| rs231456188 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526580 | AGGCATGCCCATTGA[C/T]GTACTTACATGCGTT | 68519 |
| rs231474010 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392266 | GCATGCGTGATCCTT[G/T]TGGGCCCTGTAGGTG | 68519 |
| rs231482901 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108486611 | TTTGGAGGATGGGAA[C/T]ATTGGATGCTCTGGG | 68519 |
| rs231488742 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108424011 | AAAAGTTTACCACAC[-/T]TTTTTTTTTTTTGCA | 68519 |
| rs231503862 | snp | A/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108537049 | AAGCAGGGCCGTGGT[A/G]CCTGCCGCTGCACCC | 68519 |
| rs231508302 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526971 | TGCTGAGCACCCTGA[C/T]GCTCCACCTCCCTGC | 68519 |
| rs231508317 | in-del | -/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108383533 | AGTAGTCACATTCTA[-/T]TTTTTTTAAGATTTA | 68519 |
| rs231511760 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443116 | GGCCAGCCCGGTCTA[C/T]ACCGAAAGTTTCCAG | 68519 |
| rs231525958 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108490919 | AAAATAATACATGAA[A/G]TATTCCGAAATTCTC | 68519 |
| rs231527637 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108391345 | CATCCGGGAGACAGC[C/T]TCTACACCCATCTGT | 68519 |
| rs231576796 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108496989 | CCTAACTAAAACACA[C/T]AAAGACTTGAGTTCT | 68519 |
| rs231582314 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530623 | GTGTAGCCCTGGCTG[C/T]CCTGGAACTCACTCT | 68519 |
| rs231607081 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108471142 | GGGTTTGATCCGCAC[-/A]GCAATGCTGTGAGAG | 68519 |
| rs231610735 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108495003 | CTGCACAGCCTTTCT[A/G]TGTGGGTGCTGGGGA | 68519 |
| rs231650984 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108396914 | TCTGATGACTCTCTA[C/T]TGGAGCCTAGTCCTG | 68519 |
| rs231656965 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108496247 | CCCTAGAATTTAGAT[C/T]GGAAGGCCAAACAGA | 68519 |
| rs231691425 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503610 | GTTGTAGACGTAGGC[C/T]GTCCCCGTTTATAGT | 68519 |
| rs231725632 | snp | C/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403498 | TCCCTGTGTACAGGC[C/G]GGACGGGGTATCCAC | 68519 |
| rs231726785 | snp | A/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422264 | GTTAATACCGAAAAC[A/T]TCAGAATTTTACCTC | 68519 |
| rs231761535 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469026 | ATGGTAAGGACAAGA[A/G]GACAACCAAGGCTGA | 68519 |
| rs231786275 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372651 | TACGGCACTGAGTGT[A/G]CATGGTATGTGAAGC | 68519 |
| rs231787760 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108379366 | TTCACATTTACAAAG[A/G]CTCTTGATTTTGAAC | 68519 |
| rs231788381 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519585 | CCCGCCCCTGGGAAC[C/G]GCCCACTTCCTTCTG | 68519 |
| rs231796238 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466046 | GCTATGGCCGGCGAT[A/G]CCTGGAACTGTGAGC | 68519 |
| rs231817390 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108535927 | TGTGCTTGTCTGTCT[A/G]TCTAGTGTGCGCACA | 68519 |
| rs231828231 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527784 | GCATCCACCCTACCT[G/T]CCGCTGCCCCGCAAC | 68519 |
| rs231891008 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402759 | GCTCCCGCTCTGTTC[C/T]CAGACTAGCACATGT | 68519 |
| rs231909696 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404816 | CACACACGTGCAAGT[A/G]CAAATACACACACAT | 68519 |
| rs231912918 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108386004 | GCCGAGATCTCTCTC[A/G]CTTAGGGCAATGCCA | 68519 |
| rs231952847 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108401834 | CCTTTGACTAAGTGA[A/G]AAGGAAGTAAGTATT | 68519 |
| rs231956243 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108434716 | ATACACACACATACC[A/G]CATATCATATATACA | 68519 |
| rs231957603 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108415877 | TGAACTGAGAGAGAG[A/C]TAAAGAGCCAGGACA | 68519 |
| rs231980984 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500140 | AATCCAAATCTTTAT[A/T]CAAAAGAAAATTACA | 68519 |
| rs231984873 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108462513 | AAGAGCTCACATCTT[A/G]ATCCACAGGACACAG | 68519 |
| rs232016289 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108423414 | CTGCGGGCTCCCGGG[A/C]TCCCCCATGCCCACC | 68519 |
| rs232017293 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442704 | TCCAGCCCTGAGTGT[C/T]TGATTTTTAAAAGTG | 68519 |
| rs232019896 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469320 | TCTGCTGTTGCACTG[C/T]TCAGGGTCCCAGCCC | 68519 |
| rs232031348 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447611 | GAGAGGTGATCCCTT[A/G]GAGAGAGATGTCTGA | 68519 |
| rs232057086 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108414244 | GAAAAGGCCCAGAGC[C/T]CCGTCATCTCCACAG | 68519 |
| rs232057236 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506265 | TGTGGGATGGAAGCC[A/G]AAAACCAACTCCCAA | 68519 |
| rs232077729 | in-del | -/TCT | | | intron-variant | Eml1 | Mm_Celera | 12:108456691 | CAACTAGAATCCTAA[-/TCT]TATTTTTTTTTTTTT | 68519 |
| rs232081423 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108390015 | AGGCCTGGTTCCAGG[A/G]AGGGTAGCAGCTGCT | 68519 |
| rs232111669 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108497362 | GCTGGCATTGTCTGC[A/G]CCAGCAATCCTTGTT | 68519 |
| rs232115962 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108379813 | TTCAAGGTTCTTTTT[-/A]AATTTAATTAAAATA | 68519 |
| rs232117225 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108441486 | GACCACCGTGTGAGG[G/T]GCTTCACGGAGACGA | 68519 |
| rs232147636 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108375554 | AGTTTCTTCAAAAGC[A/G]GAGTTGGTTGGGCTT | 68519 |
| rs232155534 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446795 | TATTGAGCCTCCATA[A/G]CTCAAGGCATGGCAT | 68519 |
| rs232172653 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108494896 | TGTGCGTGCACACGC[G/T]CACGCTCACCTGCAT | 68519 |
| rs232217096 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451788 | TTCTTGTACTAATGA[A/G]CATGCTGGTATAGTT | 68519 |
| rs232258480 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108502458 | TTGGGGGAGGGGGCA[A/T]ATAATTTAGACCTTG | 68519 |
| rs232266859 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108438432 | GAGGACGACACACTT[A/G]CTTTCAGCTAGTTTG | 68519 |
| rs232272655 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508880 | CATGGCCTCTCTCAC[-/T]CATGCAGCCCCAGCT | 68519 |
| rs232315452 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108394263 | CAAAACAGTAATGAC[A/C]AAAGGGTCATATTCT | 68519 |
| rs232330989 | snp | G/T | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108371012 | TAGTCTCCAGAGCTG[G/T]GTTTCCAGAGACTGG | 68519 |
| rs232334253 | in-del | -/GT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108466638 | TGTGTAGTGTGTGTG[-/GT]GTGTGTGTGTGTGTT | 68519 |
| rs232343341 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443802 | AATTTCCCATAAATC[C/T]TAAGGGACATATTCT | 68519 |
| rs232344839 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108426953 | ATGTTTCTGAGCTGT[C/T]GGACCTAAATGCTGG | 68519 |
| rs232359132 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492098 | AGTAAGAACTCTCAG[C/T]CAACTGTTGGAATCT | 68519 |
| rs232365749 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108481554 | CAGCTCAGCACTTGG[G/T]AGCCTGGGACAGTCA | 68519 |
| rs232367971 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108534367 | ATATACAAACATACA[C/T]GTGGACAAAATACAC | 68519 |
| rs232393432 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108516666 | ATGCCTTTGCTGGCC[A/G]TTTGGATTCGCTCGG | 68519 |
| rs232395514 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377957 | GTGCGCGCGCGCGCG[C/T]GTGTGCGTGTGCATG | 68519 |
| rs232398908 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108425775 | ATATATGGATGCATG[C/T]GAATGTATGTGCATG | 68519 |
| rs232400688 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433518 | TCTCTCTCTCTCTCT[C/T]TCATGCTATATAGGG | 68519 |
| rs232419690 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108447942 | ACAGGATTTCTTCTG[A/G]CCCGGGGTACCTCTC | 68519 |
| rs232433939 | in-del | -/CAG | | | intron-variant | Eml1 | Mm_Celera | 12:108394753 | TAGCTGCAGGATTTT[-/CAG]CAGGGCCCTGTGTGA | 68519 |
| rs232451383 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108496757 | ACTGGTGATCCTGGG[C/T]GCTTTAAGAAAGCAG | 68519 |
| rs232454054 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108530107 | AGTCCCAGAGAAAAC[A/C]ATCAGTGCTAACTTC | 68519 |
| rs232459856 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433042 | AGTGCCTGGCACAGA[A/G]TGGGTTTCCTGGAGA | 68519 |
| rs232503369 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108413661 | TCTGTACATCATGTG[C/T]GTGACTGGTGCCCTC | 68519 |
| rs232509247 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450917 | GAAGATCATACTAGT[G/T]TAATAAAGAGGGATG | 68519 |
| rs232525948 | in-del | -/ACACACT | | | intron-variant | Eml1 | Mm_Celera | 12:108390816 | ACACACACACCAGAC[-/ACACACT]ACACACTACACACTA | 68519 |
| rs232532854 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108525199 | TTTGGAATATATTTC[-/TT]TTTTTTTTTTTCTTT | 68519 |
| rs232537160 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108436096 | CTGCTCTCCTTCCCT[-/C]CCCCTGCCCCCTATG | 68519 |
| rs232547152 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457313 | AGCCTATAGCAGGGT[C/T]CTGAGAACCAAGCAG | 68519 |
| rs232549616 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108450161 | CGTCTCGTGCTACCT[A/G]CTGGCACTTCCGCAG | 68519 |
| rs232571188 | in-del | -/CACACA | | | intron-variant | Eml1 | Mm_Celera | 12:108485554 | AGGCACCCACTCATT[-/CACACA]CACACATACACACAC | 68519 |
| rs232581688 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108454761 | GCTGGGGTTCAACAA[A/G]ACAAAGAAAAGAAAA | 68519 |
| rs232605000 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108415302 | TCCCATGGTGCCTAC[A/G]TTATTGTATGTGGGA | 68519 |
| rs232609908 | in-del | -/AAACCAAACCAAACCAAACCAAACCAAACCAAACC | | | intron-variant | Eml1 | Mm_Celera | 12:108474933 | AAATCCTGTCTTGAA[lengthTooLong]AAACCAAACCAAACC | 68519 |
| rs232621421 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462002 | GTGTGCTGATTGTAA[C/T]AGAAGGAAGGCTCTG | 68519 |
| rs232636626 | in-del | -/TCCACTCAGTGAA | | | intron-variant | Eml1 | Mm_Celera | 12:108394490 | AAGGAGTCATTGCTT[-/TCCACTCAGTGAA]TCCAGGGGATTGAAC | 68519 |
| rs232648890 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108465937 | GTAGGAGAGTAGAAG[A/G]GGCAAGCCAGGACCA | 68519 |
| rs232663430 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456609 | CCCAATCGAACCACC[A/G]CGTGAAGGAAAATGC | 68519 |
| rs232668652 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517687 | ATATAGTCCAGGATG[A/G]CTTTAAGCTCATTGT | 68519 |
| rs232682547 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473848 | CCCCAGTGCAAGCAA[C/T]TTAGGAATAAAGGTT | 68519 |
| rs232701893 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108398758 | AGAAAATCCAACAAT[C/G]ATCAGACAAAGATGT | 68519 |
| rs232702720 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525675 | GTCTAAATGTAGCCG[G/T]GCGTGGTGGCACACG | 68519 |
| rs232713442 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390305 | ACATCTAGTCTGATG[C/T]TGGCTTCCATACACG | 68519 |
| rs232716992 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108430373 | AGAACCAGGTACAGG[A/G]GGCTGGAGAGATCAC | 68519 |
| rs232770496 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108495828 | AGGCGGTGGCCGCCC[C/T]CTGTTCTGCCCTGGA | 68519 |
| rs232771920 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108436602 | AGAGACAGGCATATG[A/T]GCTGGGCTGGGAATT | 68519 |
| rs232772006 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108487758 | TAAACAAGCCTGTCA[-/C]CAGTGACAGAAGCTT | 68519 |
| rs232783887 | in-del | -/TGTA | | | intron-variant | Eml1 | Mm_Celera | 12:108458672 | TAAGTAGTGTGTGTG[-/TGTA]TGTGTACATGGAGGT | 68519 |
| rs232808716 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108424038 | TGCATGTTGGGAGTT[A/T]TTGCTTTATCAGAAG | 68519 |
| rs232827786 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503074 | TCATGTCAAGATACA[C/T]ACAATATCCCCCTTG | 68519 |
| rs232828939 | in-del | -/TAA | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370213 | GCGAGCAGAGGTCCT[-/TAA]TTCAGTTTCCAACAA | 68519 |
| rs232841978 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108505505 | AAGTCTTATTTAGCA[-/T]TCTTGTTGCATCTCT | 68519 |
| rs232875910 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502099 | AAGCCAGGTGGGCAC[C/G]GTAGCGCTCTTGTAA | 68519 |
| rs232884247 | in-del | -/AACAACAACAAC | | | intron-variant | Eml1 | Mm_Celera | 12:108373005 | AGAGACCTTTTCCCA[-/AACAACAACAAC]AACAACAACAACAAA | 68519 |
| rs232908751 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108476955 | TTGTTTACTGGCTTG[C/T]TCAGCCTGCTTTTTT | 68519 |
| rs232911639 | in-del | -/AAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108415366 | TGTGATGGCATAGTT[-/AAAA]AAAAAAAAAAAAAAA | 68519 |
| rs232923374 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403011 | ATTTTTATTGACAGG[C/T]GAATGGTTTTACATA | 68519 |
| rs232933230 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470513 | GAAGGTATTGGATCC[G/T]TTGTAACTGGAGTTG | 68519 |
| rs232964709 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108521535 | CCTCCTGCTTCAGTT[C/T]GGTGTTCTGTGGCAT | 68519 |
| rs232970248 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432753 | TGGAGCCTCAAGGTG[C/G]CAGGATGGGAGCTGG | 68519 |
| rs232989164 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476527 | AGACAAAGGCCCACC[C/G]TCATCCCTTGGCATG | 68519 |
| rs232996458 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508239 | CAACTCCTGCAAACT[A/T]ATCCTCTGACTTCAC | 68519 |
| rs232996785 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108501416 | TCTGTTGATGGACAT[A/G]TGGCTGGTTCTAGCC | 68519 |
| rs233010789 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108419085 | TCTCACATCCCAGTG[C/T]CCATCTGTCATTTCT | 68519 |
| rs233019847 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477732 | GTTTCCTTTCGGATC[A/G]GGAGGGAATACACCC | 68519 |
| rs233023003 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108483494 | CAGGCTTTTGTTTTC[A/T]GTCCTTCATCTGAGC | 68519 |
| rs233028106 | in-del | -/CCATCTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108452115 | CGCTTCTCCTGCATG[-/CCATCTTT]CCGTCTTTTATCATG | 68519 |
| rs233036889 | snp | C/T | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108370407 | CCCTGGTCCCAGGGG[C/T]GGGGGGATAAGACAG | 68519 |
| rs233046154 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108529179 | AAGAACAAAACAACA[A/G]TAACAACAACAAAAG | 68519 |
| rs233056686 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464979 | CCCTCTCTCTCCTTG[C/T]TTTTTTTGTTTGTTT | 68519 |
| rs233068882 | in-del | -/GCCACAGC | | | intron-variant | Eml1 | Mm_Celera | 12:108392241 | TCCACCCTGCCTTCT[-/GCCACAGC]GCCACAGTGGCATGC | 68519 |
| rs233082080 | in-del | -/TAAAAAAAAAAAAAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108535528 | TCCCTTTGTATCGAT[-/TAAAAAAAAAAAAAAA]AAAAAAAAAAAACAA | 68519 |
| rs233094660 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482679 | GTAAGGATGTTTTTA[A/G]AGATGTGCTTTAATC | 68519 |
| rs233096586 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472582 | GAAGTGGTGCAGAGG[C/T]TAAAACACTGCCTGT | 68519 |
| rs233120649 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108394205 | GACATCTTGACCCTT[A/G]GAATTCAAGACTGGC | 68519 |
| rs233122478 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377601 | AGAATCCCAGGGCAA[A/G]CATACAGGGGAGCCG | 68519 |
| rs233130712 | snp | A/T | | | intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108537743 | CACACACACACACAC[A/T]CACTCTCTGCCTACC | 68519 |
| rs233148716 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381040 | CAGTAACAGGGAGAG[A/G]GGCAGGTAGCATGGA | 68519 |
| rs233153540 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471498 | AGGGGAGAAAGAGCA[-/G]GGGAGGGGGAGCAAG | 68519 |
| rs233170432 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108427877 | AGACACTGGGGGAGG[A/T]GGGGAGGGGGTTGCT | 68519 |
| rs233176640 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471225 | AGGGAGTGGAGAGGG[A/G]ACAGGAGTGGAGAGG | 68519 |
| rs233200654 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108446438 | TTGTTTTCCTTAAAC[-/AG]GGGAAAATGAAAGGG | 68519 |
| rs233201747 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108377234 | GGGCAGTATTCCTGA[A/G]GAATGCCAGCCCAGC | 68519 |
| rs233220865 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455163 | CTCTCTCTAGCCTTT[C/G]TCTCTCCCAACATCC | 68519 |
| rs233221723 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524151 | TTAATCCCAGCACTC[A/G]GGAGGCAGAGGCAGG | 68519 |
| rs233259888 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530435 | AAAGAATACAGTTTT[G/T]TACAAGAAACAGGTT | 68519 |
| rs233263837 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108480184 | ATGTGGGCTTATAGA[A/C]ACCATGCTGTGTGCA | 68519 |
| rs233292880 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478351 | GATTTATTTTTTTAA[G/T]AATGTTTAAAGATTT | 68519 |
| rs233294258 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108373822 | CTTAGGCCTGGGCGG[C/G]CAAGCCTACAGGAGG | 68519 |
| rs233300200 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108470801 | CACCATCCCCTGGGT[A/G]GGATGTCTCGAATGC | 68519 |
| rs233343328 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108420953 | GAGCATAAAGGTTAG[A/G]AGGGGAGCAGGGGAA | 68519 |
| rs233351649 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479465 | CGTGGATACTGGTCT[C/T]TATTGTTCCTTTACC | 68519 |
| rs233352933 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466775 | CACATGTTGGGTGTC[A/G]GGTGTGTCTATTCAG | 68519 |
| rs233385932 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486401 | ATCAGGCACCAGTGC[C/T]CTGCACCAGTGGCAG | 68519 |
| rs233398918 | in-del | -/GGGCCATC | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108420861 | GGTTCTTACTTCACT[-/GGGCCATC]TTCCGGGCCCACAGC | 68519 |
| rs233399027 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108505043 | TTAAAAGTAAAGTTA[C/T]TTTAATAGAAATATT | 68519 |
| rs233399380 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504631 | CTGGGTTAGATATCA[C/T]CGATTCTGGATTCTC | 68519 |
| rs233403650 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108445358 | CAAGAACAAAGCAAA[A/G]CAAAACAAAACTTTT | 68519 |
| rs233441994 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108405593 | CTCATGTGACAACCT[C/T]GGGTGGCATCCTTCT | 68519 |
| rs233452744 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508266 | TCACTTGTACACAGG[C/T]CCCTGTGCCCCTGTG | 68519 |
| rs233458730 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474319 | GGACAACCAGGGCAA[C/T]ACAGAGAAACCCTGT | 68519 |
| rs233464972 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108512236 | GATGTGCAGGCAGGT[-/G]GGGGGTGAGCGTGCA | 68519 |
| rs233466422 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464755 | AGTCCCCACTGCATG[A/T]GGTGGCATGGGTTTA | 68519 |
| rs233467954 | in-del | -/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108483569 | GGAAATGTTTTATTT[-/C]TTTTTTTTTCTTCTT | 68519 |
| rs233475675 | in-del | -/AC | | | intron-variant | Eml1 | Mm_Celera | 12:108499241 | CCCACCCACACACAC[-/AC]ATATACACACACACA | 68519 |
| rs233488879 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526081 | ACTGAGAATATGCAG[C/T]TTCATCTCTCCCTCT | 68519 |
| rs233493428 | in-del | -/AG | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405362 | GCTCAAAAGGCTTGC[-/AG]AGTCTGGACCAGGGA | 68519 |
| rs233505328 | in-del | -/GTG | | | intron-variant | Eml1 | Mm_Celera | 12:108466744 | GTGGTGTGTGTGTGT[-/GTG]GTGTGTGTGTGTGTG | 68519 |
| rs233517872 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108511264 | GAAAGTGTATTTCCA[-/TT]TTTTTGGCATCCTGA | 68519 |
| rs233523432 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527515 | AGGATGGACAAAGAA[A/G]TTCCAAAGGCAGGCA | 68519 |
| rs233524636 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504080 | TGAGGTGCTGAGAGC[C/T]GCTTCTGGCCCACAA | 68519 |
| rs233524648 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108511670 | TTCCTTAGGTCACTG[C/G]GAATGTTTTCATTGA | 68519 |
| rs233580881 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108510893 | GACGTCCAAGCTGGC[A/G]TCCACGAGTGACTGT | 68519 |
| rs233610921 | in-del | -/TC | | | intron-variant | Eml1 | Mm_Celera | 12:108425756 | TGTATGTGTGTGTAT[-/TC]GCATATATGGATGCA | 68519 |
| rs233637973 | snp | G/T | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369619 | TCTGAGTTAGAAAAG[G/T]CCTCAGTGCCCGTGC | 68519 |
| rs233653333 | snp | C/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538903 | GCACCCCGTCTCTGT[C/T]CATGCACCTCGATTC | 68519 |
| rs233665488 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108500558 | TCACTTTGATCGTTA[A/G]CTTGCCCCAAGCCGA | 68519 |
| rs233668099 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402172 | GTGCCCCATTATGGT[C/T]TGGCTGATACATTAT | 68519 |
| rs233668644 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108491304 | CAGTGTGGTGTCACT[-/C]CCCCCCCCGCCCCCC | 68519 |
| rs233676666 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379895 | ACTATGTAGCCCAGG[C/T]TAGCCTCAAAATCAC | 68519 |
| rs233689775 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404845 | ATGCACATGCAAATA[C/T]ACACACACACATGAA | 68519 |
| rs233728224 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506964 | CATGACTAAGAAGCA[A/G]GTTGGGGAGGAAAGG | 68519 |
| rs233742105 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503501 | AGCCCTGCACCGCTG[A/T]CCTCTCCCCACAAGC | 68519 |
| rs233749071 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108458987 | CTGCCTGCCTGCCTG[-/C]CTGCCTGCTGCCATG | 68519 |
| rs233777111 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108509960 | TCTGAGAAGGAAATG[C/G]TATTTTCCCAACAAA | 68519 |
| rs233796922 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379308 | CACCGGTGCTTGAGC[A/T]CATGGGTGGGGTCAG | 68519 |
| rs233850901 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108509257 | CCCCACAGACAGGTC[A/G]GCAGGACATAGGTGA | 68519 |
| rs233863087 | snp | A/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404819 | ACACGTGCAAGTGCA[A/T]ATACACACACATGCA | 68519 |
| rs233873031 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108423784 | CTTATTTATTTTGTT[A/T]ACGGCATCATAGATT | 68519 |
| rs233879650 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378472 | GCATCTATTGGGATA[C/T]TTCCATACCGACCCG | 68519 |
| rs233896783 | in-del | -/GAGGGC | | | intron-variant | Eml1 | Mm_Celera | 12:108484280 | TAGGCGACCGGTAGA[-/GAGGGC]GTGAACTGGAGCCAC | 68519 |
| rs233932934 | snp | C/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108401539 | AATGCAGGGTGTGCT[C/G]TCTGTGGCCAAGATA | 68519 |
| rs233933708 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384432 | GTCCAGGACTGGAAT[A/G]ATGTTGCCTGCCACC | 68519 |
| rs233943371 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378200 | AAGTCTAAATAAGTA[C/T]CGGAAGTCGCTGAGG | 68519 |
| rs233986819 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476921 | CGGCAGGAACTGAGG[C/T]AGAGGCCATAGAGGA | 68519 |
| rs233987126 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108424964 | AAACAGCTGTTGAAT[G/T]TGCTTCCCTTGAAGA | 68519 |
| rs233999931 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108455072 | GTGCATGTGTGTGCA[-/TG]TGTGTGTGTGTGCGT | 68519 |
| rs234009989 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460148 | ATCGCCAGTGTCTCC[A/G]AAGATCAGGCTTTGC | 68519 |
| rs234014189 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455918 | GGTTTGGGGTAAAGA[C/G]CAGAGAATAAAACAA | 68519 |
| rs234016468 | in-del | -/CACACACACA | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409671 | TCTCTCTGCCACACT[-/CACACACACA]CACACACACACACAC | 68519 |
| rs234018212 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108528671 | GTCTGACTCAACAGA[A/G]CAGCCCTCAAGGGAT | 68519 |
| rs234027161 | in-del | -/TTTTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108478724 | GCTTCTGGCTTTTGA[-/TTTTTT]TTTTTGTTTGCACAC | 68519 |
| rs234097719 | in-del | -/TTT/TTTT/TTTTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108508055 | GGCATTTTGGCAGGG[-/TTT/TTTT/TTTTTT]TTTTTTTTTTTTTCA | 68519 |
| rs234103469 | snp | A/C | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407849 | ACGTGTCAGAGGATG[A/C]GTGATTTGGGGATCA | 68519 |
| rs234110392 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524460 | AAGAAATAAAAAAAA[C/T]TAATGGCTTTTTATA | 68519 |
| rs234135727 | in-del | -/TCC | | | intron-variant | Eml1 | Mm_Celera | 12:108515713 | TTTTTTTTTTTTTTT[-/TCC]CCCTTTGGTTTTTTG | 68519 |
| rs234136992 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108513937 | GAATATGGATTGAGC[G/T]CTGCTAGAGCAGCTG | 68519 |
| rs234141286 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527972 | ACCTGGAGGAAAGCC[A/G]GATCTGTCAACACGT | 68519 |
| rs234159492 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108415441 | ATACTACCCTTGCAG[A/C]GGACCCAAGTTCAGT | 68519 |
| rs234183810 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108533780 | CATCCCTCACTCCAT[C/G]CTCTGCACCCCTCCC | 68519 |
| rs234216854 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108380680 | AGCTCGTTCATGGGA[C/T]ATAACCCCTCCTACT | 68519 |
| rs234229116 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108485493 | CACTCATTCACACAC[-/AT]ACATACACACACACA | 68519 |
| rs234235398 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374424 | TGCACCTGGTTGTTG[G/T]GTGACTCTGTTTCCT | 68519 |
| rs234255808 | snp | A/G | | | intron-variant, synonymous-codon | Eml1, Gm33385 | Mm_Celera | 12:108401131 | AGCAGAGTGCCAGAG[A/G]AAATCAGTCCCATGG | 68519 |
| rs234257777 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476222 | TTCACCGCTTATTAA[A/G]TGTGTGACTTGCAGG | 68519 |
| rs234258811 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519847 | GCTCTGCCACCACCC[A/G]GCCACATCTGCCTCT | 68519 |
| rs234308092 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478406 | TATTTAAGATTTTTA[A/T]AAAGATTTATTTATT | 68519 |
| rs234320031 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108386793 | CTTGTTACAGTTGTG[C/T]TGGTCATTGGAGGGC | 68519 |
| rs234321088 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm33385 | GRCm38.p3 | 12:108400571 | GCCTAAGGCCATTGA[A/G]AAACACAGATATTTA | 68519 |
| rs234332092 | in-del | -/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456694 | ACTAGAATCCTAATA[-/T]TTTTTTTTTTTTTGA | 68519 |
| rs234333313 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108530134 | CTTCTGAAGAGCTTC[A/G]AGCGTTTGTCAATAT | 68519 |
| rs234339576 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478295 | GTCCTACATAGTGTG[C/T]GGGGTTTTAAATGTT | 68519 |
| rs234359541 | in-del | -/ACTT | | | intron-variant | Eml1 | Mm_Celera | 12:108433273 | GCTAGCTGGACACTC[-/ACTT]ACTAAGTAGAAGCAT | 68519 |
| rs234377935 | in-del | -/AAA | | | intron-variant | Eml1 | Mm_Celera | 12:108395042 | TTAGCATTTAATGAG[-/AAA]AAAAAAATATATATC | 68519 |
| rs234381531 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108493815 | CGAGCGAAGAGATTG[A/G]TTCACCTTCGCGGGA | 68519 |
| rs234383952 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485870 | AGCACTTTTCTCCTC[C/G]GACTTTTTTTCTCAT | 68519 |
| rs234390617 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406265 | TTTTTCTGCTGTTTT[C/T]GATGACATGGAATCT | 68519 |
| rs234442033 | snp | G/T | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108535994 | AGGAACCAGAGACTG[G/T]TCAATGGGAGAAGCC | 68519 |
| rs234446976 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108457729 | AATTCATGAAAACCC[A/G]TGTTTGTTTTGAATC | 68519 |
| rs234456446 | in-del | -/ATCGGGAGGG | | | intron-variant | Eml1 | Mm_Celera | 12:108385855 | GTCACCCGAGGGCAC[-/ATCGGGAGGG]CACATCCCCAACAGC | 68519 |
| rs234479511 | in-del | -/CG | | | intron-variant | Eml1 | Mm_Celera | 12:108529938 | GCCTGTGAGCGGCAT[-/CG]TTCCGATACTTAGCA | 68519 |
| rs234481872 | in-del | -/CA | | | intron-variant | Eml1 | Mm_Celera | 12:108455071 | GTGTGCATGTGTGTG[-/CA]TGTGTGTGTGTGCGT | 68519 |
| rs234484122 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108434362 | TTGGTGCTCACCTTA[C/G]TCGGCCAGCTCTGCT | 68519 |
| rs234486581 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108463229 | GTAAGCAGAGTCTGA[C/T]ATCACTTGGACCCTC | 68519 |
| rs234525795 | in-del | -/AG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451517 | CCTACGGAGGAAAAC[-/AG]AGCAACTGTAAACTC | 68519 |
| rs234526905 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402409 | CCTTTCCTTCCCCTC[A/C]CATCTGTTTTTGAGA | 68519 |
| rs234549768 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108440908 | CGGCCTGCTCCCGTC[A/T]CTTCACTGCCACGTT | 68519 |
| rs234553565 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108430757 | CCACCTGCAAAAAAA[A/C]CCCAGGTAGACACAC | 68519 |
| rs234573786 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451010 | AGTAAATGACCAGGG[A/G]AAACCAAGGAGGTAC | 68519 |
| rs234580259 | snp | A/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536688 | CGCCCCCTAGTGGTT[A/G]TGTGGATGATGTTAT | 68519 |
| rs234588762 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409496 | AGAGTTCATTCCTCA[A/G]TTGAAACAACTCAAA | 68519 |
| rs234612488 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108440582 | TTGGTCTCATTTTCC[A/C]GCTCTCGCTGCTCAT | 68519 |
| rs234616404 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475365 | CTCTCTGTCATTAAA[A/T]ATTTCAGCTCTCCAT | 68519 |
| rs234648580 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403394 | CGCCACCACTGCCTG[G/T]CTGCATCTGTCTTCT | 68519 |
| rs234654521 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108526829 | GCCCAAGACTGGCTC[A/C]GGTGCTCCTGTCCTC | 68519 |
| rs234664564 | snp | A/C | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108536070 | TGAAAGGCAGACCCT[A/C]CTGAGACCCAGATTT | 68519 |
| rs234665841 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108482398 | GCCCTGATGCACACG[C/T]ACCACACAGCACTCG | 68519 |
| rs234671378 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507034 | AAAGGAAGTCAGGAC[A/T]GGAACTCACACAGGG | 68519 |
| rs234679412 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108439487 | CTTTGGACGTACCGG[A/G]AGAAGGCATCAGATC | 68519 |
| rs234680919 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108432567 | GGGTTCAGGAGAGAC[C/T]GTGGGTGACAGCATC | 68519 |
| rs234681060 | in-del | -/TTTT/TTTTT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108495256 | GTTTGCCTTGCTGTC[-/TTTT/TTTTT]TTTTTTTTTTTTTTT | 68519 |
| rs234696984 | in-del | -/ATG | | | intron-variant | Eml1 | Mm_Celera | 12:108508570 | TCATTTTAAAAAAAA[-/ATG]TGTTCATACCAGACC | 68519 |
| rs234699110 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532975 | GCTAGACAAAGCTGA[C/T]GTCAGTCTTGCTGAA | 68519 |
| rs234702689 | in-del | -/TTGG | | | intron-variant | Eml1 | Mm_Celera | 12:108453448 | GCTGGCCACTAAGCC[-/TTGG]TTGGAATCCTCCTGC | 68519 |
| rs234709561 | snp | C/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402963 | CTCTCTCATGGAACT[C/G]CCACCTCCTGTCTTA | 68519 |
| rs234718791 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108459729 | ACATagatagataga[C/T]agacagacagacaga | 68519 |
| rs234741747 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535338 | GGAGGGAGGATTTAC[C/G]GAGTACCTGCTACAT | 68519 |
| rs234766447 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108507521 | CAAACCAACCACTTG[-/T]TTTTTTTGAAACAGG | 68519 |
| rs234774243 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410505 | AGAATAATTATCCAA[C/T]TGCAGAGGTACAGGC | 68519 |
| rs234779294 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108534528 | AAGATACATTGAAAA[A/G]CAATGTTTTCCCAAT | 68519 |
| rs234794282 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403539 | GTGGCTACTCCGGCT[G/T]TTTCCACCCTTGTCT | 68519 |
| rs234829532 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108399458 | ATGTCAGCAGAGCTT[C/T]ATGGAGGAGGAGGCA | 68519 |
| rs234834467 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108430149 | AGCCTCTTATATGCT[A/C]TTATGACCATCGATG | 68519 |
| rs234841404 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452357 | GCAGGCCAGCTTGCA[C/T]GTGGCAGCTTGCAGG | 68519 |
| rs234865702 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108466984 | TGGTGAGCCACCCAA[C/T]GTGGATACTGGTAAC | 68519 |
| rs234865762 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108460302 | TTTTAGATTTCAGAC[A/G]TTTGCCATGGCCACT | 68519 |
| rs234879939 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108458845 | GGCCTTGCTGGAGGA[C/G]ACAAGTCACTAGTGG | 68519 |
| rs234903069 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466153 | TCAAACCTCATCTTC[A/G]TGCTAGGGACTTTCA | 68519 |
| rs234911988 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108508267 | CACTTGTACACAGGC[A/C]CCTGTGCCCCTGTGC | 68519 |
| rs234940331 | in-del | -/TTTGTTTG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452137 | TTTATCATGACAGTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 68519 |
| rs234959321 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454213 | CGGCTTTCTCAAAAC[G/T]ACCTCCTTCCAGGGC | 68519 |
| rs234967724 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503803 | GGCTTTCGGAAATGC[C/T]ATTGTATGGGCGTTA | 68519 |
| rs234971743 | in-del | -/GA | | | intron-variant | Eml1 | Mm_Celera | 12:108395955 | TAGGGATTGCTTTGG[-/GA]GAAGAGACTCAGCAT | 68519 |
| rs234990932 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453496 | TGGTGGGGTTACAGC[C/T]ATGTGCTGCCCTCTG | 68519 |
| rs235017820 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108377672 | AGCATGGTTGAGAGA[A/G]CAAGATGTTCTATTT | 68519 |
| rs235036185 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108427009 | TACACGCGCTTAACC[A/G]CTAAGCCATCTCTCC | 68519 |
| rs235040196 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108385913 | CCCAGCCTCTGGCAG[-/A]CTTCAGTCGGGCTTC | 68519 |
| rs235047542 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108393576 | GGACACCTCGGAGTC[C/T]CAAGGAACCTGTGAG | 68519 |
| rs235057670 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108464785 | CAGGTTATGGTTCTA[-/G]GTGCTAGAGAAGATG | 68519 |
| rs235065622 | in-del | -/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407046 | TATGGACATAACACA[-/T]TTTTTTTTACCCATT | 68519 |
| rs235066342 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108373718 | TCATCTGGAGCCTGT[-/A]AAAAAAATGTGGTAC | 68519 |
| rs235085474 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108441958 | AGGGACTAGTATATC[A/C]TGGTGACCCACATAC | 68519 |
| rs235087807 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108382839 | GAAGGTCAAAAGACT[A/G]ATGATCGTTGGCCTT | 68519 |
| rs235102628 | snp | C/T | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108401016 | GGCTCAGTCCCAGCC[C/T]GCAGGGCTCACCTTG | 68519 |
| rs235142581 | snp | G/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407695 | GGGTTCTCTGGAAGA[G/T]CAGAAAGCAGTCCTG | 68519 |
| rs235155694 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108498721 | ACACCTGTGCACCAT[A/G]AAGAAAGAGTGTTGG | 68519 |
| rs235167588 | snp | C/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538731 | CCATAAACTCCTCCC[C/T]TTGGGAGGCTGGCAA | 68519 |
| rs235171728 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441615 | CAGCCCAAGGCTCAC[C/G]TTAGACATCTTGAGT | 68519 |
| rs235189120 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455621 | GACTGAGGGTTCAGA[A/G]GTGGCACCTTCTGCT | 68519 |
| rs235200096 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108505637 | AAATATCAAAAGATA[A/T]ATTTTGATTCCGAGA | 68519 |
| rs235221335 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462083 | ACAATTGCCACCCCT[C/T]TTCGCTGTGACATGG | 68519 |
| rs235229529 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108519348 | CCACCTCACAGAATG[C/T]CATTCCTTTTCTTCT | 68519 |
| rs235240524 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108483320 | CTCTTGCAAGCTGGT[A/G]CCCCTGCCATGTCCC | 68519 |
| rs235243406 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108372975 | GAAAGCAAAATGGAA[-/AG]AGAGAGAGAGAGAGA | 68519 |
| rs235249730 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455510 | GCAGTGGAGGAGTTG[C/T]TCTTCCGATGTTTGT | 68519 |
| rs235252455 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108492254 | GGACAGCTGTGCTGG[G/T]CTCTCTGGCCTCTCC | 68519 |
| rs235254865 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108420040 | TAAGCCTTTAAGAGA[-/TT]TTTTCTTTCCTTGAA | 68519 |
| rs235256257 | in-del | -/AAAATGGGCAGG | | | intron-variant | Eml1 | Mm_Celera | 12:108442181 | CGTGGGGAAATGGTA[-/AAAATGGGCAGG]AGAGAAAGGTTTCTG | 68519 |
| rs235261382 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475263 | TTTTTTTTATTGTAA[C/T]AAAAGCCTCCTAGCA | 68519 |
| rs235262192 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108386264 | GGAATATGGGGTGTC[A/C]TCTCTCTGTGATTTT | 68519 |
| rs235319116 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482616 | GAACTCAGGACCTTC[A/G]GAAGAGCAGTCCGTG | 68519 |
| rs235338781 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108456530 | CATGCTTCAAAATCC[A/C]CACAGTCTTTGTGGT | 68519 |
| rs235351199 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108490633 | CTCTCACTGGGGCTT[C/T]GAGCTCTAGGGAATC | 68519 |
| rs235351309 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482031 | TAGCTCAAGAAGTCA[A/G]CTTTGTATCGAAGAG | 68519 |
| rs235363297 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108392366 | CTACAGGATGACCTC[A/G]GGGGTTCCCATTGGT | 68519 |
| rs235366138 | in-del | -/CA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485341 | TATGTTCTTTGAAGC[-/CA]CACACACACACACAC | 68519 |
| rs235367438 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108462713 | GAAGTTGGTGTGGTA[A/G]GTATGTAGTCAGTGA | 68519 |
| rs235370273 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455670 | GGGCTGGAAGCTTGG[C/T]GTCTTCTGCTCTGGG | 68519 |
| rs235419003 | in-del | -/AACAACAACAACAAC | | | intron-variant | Eml1 | Mm_Celera | 12:108373004 | AGAGACCTTTTCCCA[-/AACAACAACAACAAC]AACAACAACAACAAC | 68519 |
| rs235420106 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108489275 | TAAAGCTTCCAAGTT[A/T]GAAACTTTGTGGGGA | 68519 |
| rs235426328 | in-del | -/GTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108425829 | CACATATGGGTGCAG[-/GTGT]GTGTGTGTGTGTCTG | 68519 |
| rs235426893 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437312 | GAGGGAGGTGTGTGC[A/G]CAGCCAGAGGGTTAG | 68519 |
| rs235439850 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482516 | ATTATATGTAAGTAT[A/G]CTGTAGCTGTCTTCA | 68519 |
| rs235442843 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108462165 | TAAAGTGTGTCTGTT[A/G]GGCCATAAGATGGAT | 68519 |
| rs235480036 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108514783 | CACTGGTTGCTAGGG[A/C]CTGGCAACCTGGCTT | 68519 |
| rs235527423 | in-del | -/GTGGTT | | | intron-variant | Eml1 | Mm_Celera | 12:108527355 | AACTGGCGGTGGTCA[-/GTGGTT]GTACTCCCAGATAAA | 68519 |
| rs235530859 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108390047 | CCCTTAAAAAAAAAA[A/C]ACACACACACACATT | 68519 |
| rs235555436 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108507621 | TAGGTATGAGCTTAC[A/G]CTCCCCTAAAGAGCT | 68519 |
| rs235557790 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462530 | TCCACAGGACACAGA[G/T]CACACTACCAATGCC | 68519 |
| rs235568044 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108381244 | GCTGAAGAAGTACAT[C/T]CCAGATCTGTGAACC | 68519 |
| rs235569946 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416726 | CAGTTGTTTGAAAAA[A/G]ACTGATAGGTTTATG | 68519 |
| rs235570289 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108515244 | CTCCTAAAGCCATTC[A/G]ATGTCTTTGGTAATG | 68519 |
| rs235581109 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432454 | AGGTCGCTGTCAGTG[C/G]TGCAGAGGGTAGTCT | 68519 |
| rs235583869 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108409557 | TCCCATACATATACT[C/T]CCTCTCTGTCTCTCT | 68519 |
| rs235604700 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108521861 | TGAATTAACAGTGAA[A/G]AGGATAGGCTCAGAG | 68519 |
| rs235627790 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108424753 | TGGTAGCTCAGTCAT[A/T]CAGTTGTTTTATTTG | 68519 |
| rs235628972 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438585 | TCAGGTGAGCAAGCA[C/T]GACTTTGTCCCATTT | 68519 |
| rs235631755 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108464918 | CTCTCTCCCTCCCCT[-/C]CCCCTCCCTCTCCAC | 68519 |
| rs235632721 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108515625 | ACAGATGCGCACAGG[G/T]CAGCTCAGAGGCTGA | 68519 |
| rs235649505 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108484258 | CTTCCCGCAGGAAGG[G/T]CCTGGTTAGGCGACC | 68519 |
| rs235659556 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108390477 | TGTAGTAATAATAAT[-/A]AAAAAATTAAAAAAT | 68519 |
| rs235667760 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460021 | GCTGCTTGTGAGGAC[A/G]CCAGTCTTGTCAACC | 68519 |
| rs235677764 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108521524 | CAGTGTGGTGACCTC[C/T]TGCTTCAGTTCGGTG | 68519 |
| rs235680542 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108534416 | ATCTAAAAGTTATAA[C/T]TTAGAAGTTTGAAAG | 68519 |
| rs235711320 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108387939 | TGGTAGATGTCTGCT[A/G]AATGTTTCTGTGCCA | 68519 |
| rs235713907 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374585 | ATTCTCTAAGAAGGC[C/T]CTGACATCCTCGCAG | 68519 |
| rs235721648 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108434099 | CCTTGGTTGATTCTG[A/G]CAACAGGGCTCCGGA | 68519 |
| rs235729970 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108439622 | CTGCCCCACATAGCA[-/C]CCTTTTTTTATTTTC | 68519 |
| rs235734222 | snp | G/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421702 | AGTGCTGACTCTGGC[G/T]GTCCAGGTCACACCC | 68519 |
| rs235747296 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108394481 | ACCAATCTAAAGGAG[C/T]CATTGCTTTCCACTC | 68519 |
| rs235756739 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108435534 | GGACAGACAGCGGTC[G/T]GTGTCAGCCACTGTG | 68519 |
| rs235758653 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403641 | TATATATCTAGAAAC[A/G]GGATTACTGGTCCAT | 68519 |
| rs235807989 | snp | A/G | | | intron-variant, synonymous-codon | Eml1, Gm33385 | Mm_Celera | 12:108401305 | GGGCTGGCTGATGTG[A/G]CTGATCCAAGGAACA | 68519 |
| rs235816896 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108388195 | GTAGAAGTCCTTCTA[C/T]GCATCCTGCAGCTGC | 68519 |
| rs235817040 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381297 | TAGCATACTGCGTAC[A/G]TGAAAAGTTGAGTGG | 68519 |
| rs235825302 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530520 | GACAGCGAACCTTTT[C/T]GTCACTGTGCAGCTG | 68519 |
| rs235825901 | in-del | -/CA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473180 | CATACCATACCACAC[-/CA]CACACACACACATAC | 68519 |
| rs235833791 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450682 | CAGCATCTGGGAGAT[A/T]GCAGGCAGCACAGTA | 68519 |
| rs235845063 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108491919 | AACTTTAAAAAAGTT[C/T]TATATGAGAAATGGC | 68519 |
| rs235904730 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108441032 | GGCTGTCACAATGCG[C/T]AGAAAGTCCTGGTCC | 68519 |
| rs235907872 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108484824 | CAGAAAAGCCATGTT[A/G]CCCTAAGACATGCCA | 68519 |
| rs235910407 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380833 | TTAGTCAGCCGTGAA[A/G]AGGACAGAAAGCCAG | 68519 |
| rs235946379 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108484406 | AGGGGAATGGGTGAG[A/G]TTTAAGGGAAATAAT | 68519 |
| rs235949775 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108487567 | ATTATAAACAAAAAT[-/A]AAAAATAGTACTTAA | 68519 |
| rs235967787 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108434696 | ATACTACACACACAC[-/AT]ATACATACACACACA | 68519 |
| rs235989338 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485004 | TGTGTGAACAGGATC[C/G]TGCTCTGTTACTTGG | 68519 |
| rs235989468 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384009 | CCTCAGAGCTCACCC[A/G]TCATAAACCATACAA | 68519 |
| rs235999067 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402862 | CCTCCTCCAGCATCC[C/T]GGGCAAAGCTCTCCA | 68519 |
| rs236016263 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535581 | ACCTTATGAATAGAA[A/G]GTTCAGATGCCAGTG | 68519 |
| rs236017628 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108434460 | GATAGTGTTGGGCAC[A/G]CCCGTTCCCAAGGCT | 68519 |
| rs236018885 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108451560 | TTGGGGGTGGTTCAG[A/G]TGTGCTCACAGTAAG | 68519 |
| rs236019168 | in-del | -/GTGTGTGTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108535886 | TGAAGAGGCTGAGGG[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs236027301 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445850 | GCAGAACTTACCAAC[A/G]ATTCCTTCAGGTATT | 68519 |
| rs236035543 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108510880 | CTGACAAATAGGAGA[C/T]GTCCAAGCTGGCATC | 68519 |
| rs236040754 | snp | A/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108413398 | GGGGGTCTTGAGAGT[A/G]ACTCCTGCACATAAC | 68519 |
| rs236063594 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108471724 | CCACTTGCCTTTGTA[C/T]CCCTGCCACTTTGCT | 68519 |
| rs236078931 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108389616 | GCCTGGAACCCAATG[C/T]CACCAATATGGAGAG | 68519 |
| rs236095338 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445221 | GAAAGTCTGTGCTTT[G/T]TAAAACAAATAGTGC | 68519 |
| rs236108348 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108510305 | CGACAACCTCCTGGC[A/G]ACATTGCTGATGATG | 68519 |
| rs236125225 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108486455 | TGATACAGTGGTCAG[C/T]GATGAGAGGGCTGTC | 68519 |
| rs236137249 | in-del | -/ACAC | | | intron-variant | Eml1 | Mm_Celera | 12:108472968 | ATACACACCAAGCAT[-/ACAC]ACACACACACACCCC | 68519 |
| rs236139461 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517988 | ACATAGAGAGTTCTA[A/G]GACAGCCAGGGCTGT | 68519 |
| rs236184192 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410074 | GCGTGCACACTTGCA[C/T]ACATCTACCACAGTG | 68519 |
| rs236202042 | snp | C/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408688 | ATGACCATGGCGTCT[C/G]AGAATTTCTGGCTGC | 68519 |
| rs236226119 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108456823 | GCTGGGATTAAAGGC[A/G]TGCACCACCATGCCT | 68519 |
| rs236229318 | in-del | -/GGGGGGG | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422757 | GTTGTCCGGGGTCCC[-/GGGGGGG]GGGGGGGGGGGACAG | 68519 |
| rs236248541 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108417161 | AGGAGAGGAGGGTAC[C/T]GACGTCAGAGATATG | 68519 |
| rs236260506 | in-del | -/CAATGTTTTCC | | | intron-variant | Eml1 | Mm_Celera | 12:108534529 | AGATACATTGAAAAA[-/CAATGTTTTCC]CAATGTTTTCCTTTT | 68519 |
| rs236262987 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433594 | GGCTAAGCAATAGCA[C/T]TTAGAGCTGATCATC | 68519 |
| rs236263296 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525156 | TTTAAATACTCTCTC[A/T]CTATGTCAGGTGGTA | 68519 |
| rs236315171 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404099 | ATCCTAGGGCTTTAC[C/T]CTGAAAAGGCTGCGC | 68519 |
| rs236323743 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108488014 | CTAGTGGTGGGCTCC[A/G]GAGCTCCCAAGCCCT | 68519 |
| rs236347831 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108453430 | GCTGGCTCTGCTAGA[C/T]TGGCTGGCCACTAAG | 68519 |
| rs236350948 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442141 | AAACTGTGGTTCCAA[C/T]CCCACGTGGCATTGC | 68519 |
| rs236356591 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442585 | GTGCCAGAAGAGGGT[A/G]TCAGATCCCATTACA | 68519 |
| rs236360787 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108487256 | ATAGATACAGAATGC[C/T]GCCATCAGCATTTTC | 68519 |
| rs236360872 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108496082 | TTGTGTCTTCTGCAG[A/G]CTGGTGTCCAGGAGG | 68519 |
| rs236400040 | snp | C/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538948 | AGCCACCACTCTCTG[C/T]GTATTGATGGCATGA | 68519 |
| rs236403469 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454626 | TTCCTTCCTTCTTTC[C/T]ATTCATTTATTTATT | 68519 |
| rs236408714 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108387877 | GTGGAGTCAGATCTC[A/G]CCCCCCTGCGAAGGC | 68519 |
| rs236431844 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437840 | TGCTGATTCCTCAGA[C/T]CTCAGCTTCAGCCTT | 68519 |
| rs236485980 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108447799 | GAGCCTGACTCCAGT[A/G]ACAGTGTCTGTAGCA | 68519 |
| rs236500335 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437411 | CCATGGCTGAGTTAC[A/G]AGATCTCACCCAGGG | 68519 |
| rs236567354 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442903 | AATATCAGTAAACCC[C/T]GAGGAATGTTACCAA | 68519 |
| rs236581200 | in-del | -/A | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403064 | AGCCCCAGCTATCTC[-/A]ACCACGTCTCAGTGG | 68519 |
| rs236593325 | in-del | -/CCC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472983 | ACACACACACACACA[-/CCC]CACACCATACACACA | 68519 |
| rs236596254 | in-del | -/GTGGGGC | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108536148 | TGGGTGATCTTCCCT[-/GTGGGGC]GTGGCTCTGAGGACT | 68519 |
| rs236600264 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378166 | ATTCTTGAGATTATA[C/T]AGTCTAAATAAGCAC | 68519 |
| rs236611238 | in-del | -/GTGTGTGAGAGTGTATGTGA | | | intron-variant | Eml1 | Mm_Celera | 12:108449649 | ATTGTGTGTGTGCAT[-/GTGTGTGAGAGTGTATGTGA]GTGTGTGTGCGTGTG | 68519 |
| rs236612986 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108459759 | ACAGACAGATAGATA[G/T]AGGATGAAACAGACA | 68519 |
| rs236618229 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108439536 | TGCCACCATGTGGTT[G/T]CTGGGATTTGAACTC | 68519 |
| rs236631722 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442448 | AAAATGAAGATTCAC[C/G]GTCCACACCACCACT | 68519 |
| rs236638105 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108384766 | TCTACCTCCCACTGT[-/A]GGATGCTAAGGATCC | 68519 |
| rs236650830 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406204 | TCTCCCTTCCTTCTC[C/T]GTCTTACTACACACC | 68519 |
| rs236655439 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108420790 | CCAGTGGGAGCTACC[A/G]CACCTAGTTTGCTCT | 68519 |
| rs236658287 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108484924 | CTTCAGACACACCCA[C/T]GCAGAGGCTCTTGTG | 68519 |
| rs236681267 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383896 | GTCTGCTCAATAGGG[C/T]GGGCTGATGCTCAGG | 68519 |
| rs236682122 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108444787 | AATCTGAGAGTACAG[C/T]TGAAGAGGTCTTCTT | 68519 |
| rs236720526 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108499638 | CCTGGAAGTATAACC[G/T]GACATTAACCCTTTC | 68519 |
| rs236757670 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480567 | AGTGTGAAGCTTCAC[A/G]CTGGAAGTGTGTGGT | 68519 |
| rs236771449 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108479347 | ATATGGTCAGTACGT[C/T]GTTTGATTTTGATTC | 68519 |
| rs236777566 | in-del | -/GGGGGG | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422758 | GTTGTCCGGGGTCCC[-/GGGGGG]GGGGGACAGCTCGAG | 68519 |
| rs236823177 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108462381 | GCTATGAGAAAACAC[C/T]ATGCTCAAGGTAACT | 68519 |
| rs236836910 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108535397 | GTGGGGGGGGGGGGA[-/A]GTGGGATGTGAGAGC | 68519 |
| rs236839760 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108495516 | GGGGGCAGGCCCCCC[-/T]CAAGGGACAGGCCCA | 68519 |
| rs236843854 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108375694 | GCATCTCTGGAGGAG[A/G]TGCCCAAATACTCTG | 68519 |
| rs236856781 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408581 | TAGTTAAATGCCCAA[A/C]GTTTCTTATTTAGGG | 68519 |
| rs236866964 | in-del | -/CAGA | | | intron-variant | Eml1 | Mm_Celera | 12:108491978 | GACATTAGATGTTAC[-/CAGA]CGGAGAAAGTGTCCC | 68519 |
| rs236874677 | in-del | -/AAATAAAT | | | intron-variant | Eml1 | Mm_Celera | 12:108518023 | AGAGATCCCATCTCA[-/AAATAAAT]AAATAAATAAATAAA | 68519 |
| rs236891724 | snp | G/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108406322 | TCTGCACAGTTGTAC[G/T]ATGTTCACTTGAGTC | 68519 |
| rs236913351 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469193 | GCAAGCACAGGTCAC[A/G]TCACTTCGCACCCAC | 68519 |
| rs236923289 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455252 | TGTGTTTTCTGGATC[A/G]GCACTAGGTGTCAGC | 68519 |
| rs236927275 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416175 | TCCCCCAAAAGGAGG[C/G]AAAGTTGGATTATGG | 68519 |
| rs236929459 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462774 | GACAAGGAAGGTGTC[C/T]AGGGCTGGGAACTGT | 68519 |
| rs236937367 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108470471 | TGTATGTGACAAATG[A/T]ATGCCTGGTGCCTAA | 68519 |
| rs236949851 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468413 | AAAAACAAAACAAAA[A/C]AGAACAAAAATAGTG | 68519 |
| rs236951884 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108428990 | CTCTGCCTCAGAGTG[C/T]TGGGGTTAAAGGCGT | 68519 |
| rs236954142 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446890 | AGAAGGGCTAGCATG[-/T]TGTGTGAACCTCAGG | 68519 |
| rs236979228 | in-del | -/ACAGGGTGCCAGA | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108539483 | GCCTGCTGTGGAAGG[-/ACAGGGTGCCAGA]AAACAACGTGACTCA | 68519 |
| rs236983237 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108395453 | TGGGGGAGGGGGAGT[A/G]GATGCAGGCAGATGC | 68519 |
| rs236988555 | in-del | -/GCAGTTAGCAC | | | intron-variant | Eml1 | Mm_Celera | 12:108387980 | TAGGGAGCTGTGCAT[-/GCAGTTAGCAC]GGGGACCACCAAGCT | 68519 |
| rs237003643 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108504679 | AGAACAGAGACTCTG[A/C]TCATTTTCCTTGCTC | 68519 |
| rs237018291 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108469868 | TCAGCCATTTGAATA[A/G]CTGTATAGAGCTAGT | 68519 |
| rs237039076 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461688 | CCCACAAGGGGACCT[C/T]CCCCCTTGATCTCTA | 68519 |
| rs237044346 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476168 | CTGGATTATGCTGTT[G/T]TTGTCCTGCAACTAC | 68519 |
| rs237052473 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108511964 | CAGGGACACATTTCC[C/G]ACCAAACATTTCTAG | 68519 |
| rs237094549 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108444051 | ATGCACTTAAATAGA[C/G]CTTGCTGCATGGCAA | 68519 |
| rs237104927 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108479011 | ATGAAAGGTTTTTTT[-/A]AAAAAAAATTATTTT | 68519 |
| rs237112939 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410724 | TCCCAACCCCATTCC[A/G]GGAGCAGTTCTGGGG | 68519 |
| rs237116947 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442965 | AGCTAAAAGTCAACG[G/T]CACTCTCCTCATTAG | 68519 |
| rs237117612 | in-del | -/AGGTTGAGGCAGGA | | | intron-variant | Eml1 | Mm_Celera | 12:108508626 | ACTCCAGAGCAAGGG[-/AGGTTGAGGCAGGA]AGATCTGAGCTAAAG | 68519 |
| rs237134713 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458329 | CAGGACTCTGGGTCT[A/G]GACTGACCCATGTTG | 68519 |
| rs237135882 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502321 | CACATCTATACATAT[A/G]TATATGTGCAAATAT | 68519 |
| rs237153815 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443689 | GAAAATGCAACCCTA[A/C]CGGGATGGCTGTTTA | 68519 |
| rs237177089 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108379392 | TGAACTTGGGGTTTT[-/G]GGCCTGCGAGGCAAG | 68519 |
| rs237197558 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379993 | TTTCTTTTTAAGATG[C/T]CCCTCTCCCTCCCCC | 68519 |
| rs237221404 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108463794 | CACTGAACCAATCTC[A/T]CTAAGGTCGACAGTC | 68519 |
| rs237242648 | in-del | -/AGTG | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404813 | ACACACACACGTGCA[-/AGTG]CAAATACACACACAT | 68519 |
| rs237246132 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454243 | AGCTCTTTTTCTTTC[-/T]TTTTTTCTTTAAGTT | 68519 |
| rs237247757 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370726 | AGCTTCCTATGCCTC[A/G]GAGACAGACAGCCTG | 68519 |
| rs237248420 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108389371 | ATGAGAAGAAGCACG[A/G]TTGGCCTCTAAGTCC | 68519 |
| rs237289749 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486126 | CTCTGCTTGTAGCAG[A/G]AGCAGAGACTGCTGC | 68519 |
| rs237290342 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108472361 | AACTCATTCTTTTAA[A/T]TTGGGCCTAAAAGTG | 68519 |
| rs237310496 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377861 | AGGCTTGGAGGAAGC[A/G]CATTTACCCACTGAG | 68519 |
| rs237317179 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108506457 | CCGAGGCATGTCACT[A/G]ACACCTTCACTGTTT | 68519 |
| rs237318565 | in-del | -/TGCGCACA | | | intron-variant | Eml1 | Mm_Celera | 12:108482423 | ACTCGCGCACTCGTG[-/TGCGCACA]CACACACACACACAT | 68519 |
| rs237335899 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108522359 | CTAATAATCATGTGG[C/T]AGGAGGCAAGCATAA | 68519 |
| rs237362249 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108382020 | TCTCTGCCTGGGGAG[A/G]CTGGCCCAGAAAGAT | 68519 |
| rs237372829 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108514113 | CCCAGTCACTAGAAA[A/G]GGGGAGGGGGTGTGA | 68519 |
| rs237378854 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108528411 | AGACTCAGCCTCCTC[-/T]CACCAGCCTCCTCCA | 68519 |
| rs237380720 | in-del | -/CC | | | intron-variant | Eml1 | Mm_Celera | 12:108512876 | TTCAAAAAAACAAAA[-/CC]AAACCAAACCAAAAG | 68519 |
| rs237409316 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108493728 | ACCCTACTCGTGCAG[C/T]CTACAGCAGGGCTTC | 68519 |
| rs237439945 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108431642 | AGACACGGACACGTA[G/T]ACACAGAACTCACAC | 68519 |
| rs237441462 | in-del | -/CCCGGCAGT | | | intron-variant | Eml1 | Mm_Celera | 12:108456408 | CTTGCTACTCTCAGC[-/CCCGGCAGT]CTTGCAGGCCAGTTC | 68519 |
| rs237450433 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388290 | GAAGGACCCACCTGA[G/T]AATCCAGGATCATCT | 68519 |
| rs237458113 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476547 | CCCTTGGCATGTGAT[A/T]CCCAGTTTCCCAGCA | 68519 |
| rs237459302 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108493123 | CTCAGGGACTGCCCA[A/G]GTTTTGTTTCTATAG | 68519 |
| rs237462748 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478686 | GGCCTCTGCTGGGAT[C/T]AAAGGCGTGCGCCAC | 68519 |
| rs237482008 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437945 | CACACCCTGTAACAG[C/G]GCTGGCTCCACTCTG | 68519 |
| rs237482125 | in-del | -/AA | | | intron-variant | Eml1 | Mm_Celera | 12:108439426 | AGTCCATAGCAACTT[-/AA]AAAAAAAAAAAAAGA | 68519 |
| rs237516039 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108483669 | ATGTCCTGAAAGAGC[C/T]ATGATGGATTATACC | 68519 |
| rs237534758 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108533911 | TCTTCCTGTCTTAGT[G/T]GTAGGACAGCTACGG | 68519 |
| rs237540021 | in-del | -/CC | | | intron-variant | Eml1 | Mm_Celera | 12:108443396 | CGCTTCTCCTCCAGT[-/CC]CCCCCCCTCCCTCCC | 68519 |
| rs237545775 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108535059 | CATCCCTCAGTGTCC[-/T]TTGTGACATGAGGAT | 68519 |
| rs237554031 | in-del | -/GTGTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108475735 | AGTGTGCCTGAGTGA[-/GTGTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs237560704 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478237 | CCCTTGACATGTTCA[C/T]GCCTGTGACAAACAA | 68519 |
| rs237574907 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108461682 | GCACCACCCACAAGG[A/G]GACCTCCCCCCTTGA | 68519 |
| rs237575100 | in-del | -/CTTGGCAGCCAT | | | intron-variant | Eml1 | Mm_Celera | 12:108428288 | GACTGGGTCACCAGG[-/CTTGGCAGCCAT]CTTGGCAGCCATCTT | 68519 |
| rs237595505 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108517772 | TCTGTATGTATTTGT[C/T]AAAACATCATGGGTG | 68519 |
| rs237595826 | in-del | -/TC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473037 | TCAAGCATACACATA[-/TC]TCTCTCTCACACACA | 68519 |
| rs237597612 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108445794 | TACCTGTTAGAAGCC[A/C]CAGAGATATGGCGGC | 68519 |
| rs237598564 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421799 | AGTCTGTCTTGTTCT[C/T]CTCCCTCCAGGCTTC | 68519 |
| rs237607588 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108419615 | TCTTCCCCTTTCCTC[C/T]CCTCCTCCTCTCCCT | 68519 |
| rs237612464 | snp | C/T | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369589 | GAGACCTTGTGATCA[C/T]AGCCCTCTGTGGCCT | 68519 |
| rs237612887 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108467691 | AGTGCTTCCTGCCTC[A/G]GCCCTTGAGTGCTAC | 68519 |
| rs237630765 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519114 | CCTGGGCATCTCGGA[A/G]GATGGTGAAGCTGAG | 68519 |
| rs237668957 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108429152 | GTGCGCGCGCGCATG[C/T]GTGCGCGCATATGCA | 68519 |
| rs237676959 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108463345 | GCCCATAGAGCGTGC[A/G]TGATGCTGGTAATGG | 68519 |
| rs237722120 | in-del | -/TTCCAATTCTTTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108518930 | TTTCCAAGTCTTTGC[-/TTCCAATTCTTTGT]TTCCAGTTCTTCATG | 68519 |
| rs237729027 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108490732 | CAGAATGGAAAGCAC[A/G]TGGCACGATCTGGAT | 68519 |
| rs237733714 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384453 | GCCTGCCACCCCTCC[A/C]TCCAGGGCTCACAAG | 68519 |
| rs237751831 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532097 | CCTGGGTCACTGCGC[A/T]TGCTGACATTTAGTA | 68519 |
| rs237756120 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108525427 | TTTAACTCCCAAAGA[A/C]TATTTTGAATGTTTT | 68519 |
| rs237757122 | in-del | -/ATACAAC | | | intron-variant | Eml1 | Mm_Celera | 12:108446457 | GAAAATGAAAGGGAT[-/ATACAAC]GTTATGGCATGGTCT | 68519 |
| rs237778218 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm33385 | Mm_Celera | 12:108400107 | AAGCAGGGTTCATCA[A/G]AGCATCTGGGTCTTA | 68519 |
| rs237791308 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108531412 | GTAGTCCCAGCACTC[A/G]GGAGGCAGAGGCAGG | 68519 |
| rs237811281 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108390195 | CACTGGGAAGGCAGA[A/C]ATAGGACGGTCACTG | 68519 |
| rs237823070 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108392175 | GAGACATGACATCCC[A/G]GTAGCTTCATGGCAG | 68519 |
| rs237827154 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474223 | GGCATGGTGGTGCAC[A/G]CCTTTAATCCCAGCA | 68519 |
| rs237833865 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108398428 | GGCAAGGACATGATA[A/G]GGAGGCTACAGGATG | 68519 |
| rs237844176 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441506 | CACGGAGACGAAGCC[A/G]TTGATGACTTTATAG | 68519 |
| rs237846742 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108525892 | AATTGTGTTGCTTTT[A/G]AGAATGTTTCAAGCA | 68519 |
| rs237850873 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442349 | GTGCATGGCCTCCCC[A/G]CCACTCAGCACCCAC | 68519 |
| rs237855921 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108497257 | AGGGAGCAGGTGAGA[A/C]ACGCCTCCGCAAGCT | 68519 |
| rs237868577 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108489043 | AAGCTCCTTTTTGGC[A/C]TTTTAACAGCCTGTT | 68519 |
| rs237892772 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108496458 | AAGGATGACTTCCGG[C/T]AGAGGTGCTTTTCAT | 68519 |
| rs237894229 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108487132 | ACTACACATGCCATC[A/G]TGCCTACGATATTGG | 68519 |
| rs237898937 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504177 | GTACTGCTAGACGTA[C/T]CAGTAAGCAAGTAGA | 68519 |
| rs237918872 | snp | G/T | | | intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108537686 | TGCAGCTATGTGGGC[G/T]TCACCCTGACACTGA | 68519 |
| rs237922293 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520942 | ATACACACATGCACA[C/T]GCTCTTGAGTGTGCA | 68519 |
| rs237925111 | in-del | -/CTCTCTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108516855 | GTTTATCACTAGAAC[-/CTCTCTTT]CTCTAGAATCCAACA | 68519 |
| rs237947893 | in-del | -/GCCTTTACCTAGTGCGC | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410186 | GGCTTAGCCACAAGT[-/GCCTTTACCTAGTGCGC]TATCCTGCTGGCCCT | 68519 |
| rs237973835 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108494770 | CCTCTTCTCAGATTC[C/T]TGGAGACCTGAGCAT | 68519 |
| rs237985295 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108503771 | ATCGGCACCCACAGC[A/G]GGCTCTCTAGCTCTC | 68519 |
| rs238011293 | in-del | -/GAA | | | intron-variant | Eml1 | Mm_Celera | 12:108396052 | GGTGGGGGTGGGGGG[-/GAA]GGAAGGCTCATTCTT | 68519 |
| rs238012838 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108432656 | CAGGAGACAGATGGA[C/T]GAGCAGAGAACAGGG | 68519 |
| rs238014719 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108423629 | AGCAAACAAATCACT[A/G]CTGGAACAAAACCTT | 68519 |
| rs238050539 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437920 | GTCCTTGCTTCCCAG[C/T]CGGGATTCACACACC | 68519 |
| rs238053182 | in-del | -/CTTC | | | intron-variant | Eml1 | Mm_Celera | 12:108447510 | TGTCTGGCAGTCTTT[-/CTTC]CTTCTTATGATCTAG | 68519 |
| rs238073067 | snp | A/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372975 | AGAAAGCAAAATGGA[A/G/T]AGAGAGAGAGAGAGA | 68519 |
| rs238078384 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466399 | CCACCTCAGTATTTG[C/G]GGTGCTTCCTTTATC | 68519 |
| rs238089282 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108393603 | TGAGCATGTGTGGGT[C/T]CTAGATTTGTATACC | 68519 |
| rs238105900 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436703 | GTAACATCTGCTTTC[A/G]GATCCAGTAGCTTAC | 68519 |
| rs238113786 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443408 | CAGTCCCCCCCTCCC[C/T]CCCTGCTTTGTTCAG | 68519 |
| rs238130832 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108431426 | CAGCACTGGGGAGCA[A/G]AGGCAGGAGGGCCTT | 68519 |
| rs238139563 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464605 | GGTGGAGCTCTGTGA[C/T]TTCTAAGACAGTCAG | 68519 |
| rs238153135 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108528352 | TCTCAGCTAGAGAGG[C/T]TTTCAGCACTGGGGA | 68519 |
| rs238153727 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108491179 | CGCAGGAGGCGCGAG[G/T]TCTGGCTGGAGTCAG | 68519 |
| rs238154944 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108534563 | TCCTTTTTGAGTAGT[C/T]CATGAATTGGTCTGA | 68519 |
| rs238160787 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108481952 | GTTTGCCTTTGTTGT[C/T]GGTAGCAAAAGTCAG | 68519 |
| rs238178840 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532696 | CCAGGGCTACACAGA[A/G]AAATCCTGTCTCAAA | 68519 |
| rs238197740 | snp | A/G | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108400836 | AAATGTTTCATGACA[A/G]AGTCAAACAGAAATG | 68519 |
| rs238229187 | snp | C/T | | | utr-variant-5-prime, intron-variant | Eml1 | GRCm38.p3 | 12:108422841 | GTAAGCGTCCCTTGC[C/T]TTCTCTCCCTTTATC | 68519 |
| rs238238303 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108385615 | GGTTTGGCCATTTGC[G/T]TCTGGGGATGTGGTT | 68519 |
| rs238247374 | snp | A/G | | | intron-variant, missense | Eml1, Gm33385 | Mm_Celera | 12:108401378 | CCTGGCTTGCGGAGA[A/G]TGTGGACAGGTGGAG | 68519 |
| rs238254887 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108489088 | GGTCGGTGAGGTTCC[C/T]GTGCTTTTCCGCCTA | 68519 |
| rs238260298 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108439427 | AGTCCATAGCAACTT[-/A]AAAAAAAAAAAAGAT | 68519 |
| rs238281843 | in-del | -/TTT | | | intron-variant | Eml1 | Mm_Celera | 12:108445437 | TGGGCGTTACCCTTT[-/TTT]GAAAGGGGTATGGGG | 68519 |
| rs238298138 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108387029 | GATGGGGAGGAGAGC[A/G]GACTCTCTGAGGAGC | 68519 |
| rs238303107 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108499498 | TCTATAAGAAAGCAG[A/G]CTGAAGCAAGCCATG | 68519 |
| rs238308306 | snp | G/T | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108400901 | TACCAGGGTGAGCAT[G/T]AATGTGGTGTAATAT | 68519 |
| rs238318594 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520108 | AGAGACCACATGGCA[A/G]GGCAGGGATCTCTCA | 68519 |
| rs238325399 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108428223 | CTATAGAAGTCAGAG[C/G]TTTTCTTCTGGGGAG | 68519 |
| rs238326196 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108505854 | GAAGCTCAAAAATAA[C/T]AACCACACAAACTTT | 68519 |
| rs238342804 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108472141 | TTGATGCCTTGCAAT[C/G]CAGGAACGGTAGGTA | 68519 |
| rs238355085 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519530 | CCGCATCTCACCAAG[A/G]CATGGAGCTTGCTTA | 68519 |
| rs238357908 | snp | A/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406815 | AGGCTCCACAGCCTC[A/T]CAGAGCAGCTGTGGG | 68519 |
| rs238363102 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524342 | TGCATCCTATCAGAT[C/T]ACCATGGCCTAAGGC | 68519 |
| rs238375574 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108495257 | GTTTGCCTTGCTGTC[-/TT]TTTTTTTTTTTTTTT | 68519 |
| rs238395298 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108523073 | gaccagaaaagaaat[C/G]cctcctgtcacataa | 68519 |
| rs238396931 | in-del | -/CTGAAAAC | | | intron-variant | Eml1 | Mm_Celera | 12:108500482 | AATTCCTGGTGCACA[-/CTGAAAAC]CTGAAAACCTGTTAC | 68519 |
| rs238405995 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404911 | ACACACATATATACA[C/T]ACACACACGTGCACG | 68519 |
| rs238444143 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527399 | TGACCAGCTTCCTAC[A/G]GGGCCAGAGGACAGA | 68519 |
| rs238447366 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445164 | ATAATTCCAGTTGGG[G/T]GTGTGTGTGTGTCAG | 68519 |
| rs238455240 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473684 | CCTGTGGCTGTTGGA[C/G]CTGCCCTACTCCATT | 68519 |
| rs238457344 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393240 | CCCTGTGCACAGGAG[A/G]TGCCTAGGGGTGGGT | 68519 |
| rs238474228 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451290 | ACAATCATGAGTGCA[C/T]GCGCACACACACATG | 68519 |
| rs238479215 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108526825 | AACAGCCCAAGACTG[A/G]CTCCGGTGCTCCTGT | 68519 |
| rs238492339 | snp | A/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413268 | AGTGGCACAGCTCTC[A/G]CCCCGTGTGCTGGGC | 68519 |
| rs238504085 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451080 | GTTTGATTGTTTATC[A/G]TGTAGATATTTAGAG | 68519 |
| rs238540845 | in-del | -/A | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405815 | GGCTAATGTCCTCTG[-/A]ATTGCTCTGAAGTTG | 68519 |
| rs238551442 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108395883 | CTGAGACTGAACAGT[G/T]TGTCTGTCTCCAGGC | 68519 |
| rs238551994 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108418740 | GTCTGTATGGAGGTC[A/G]GAGGAGGGAATTGGG | 68519 |
| rs238555328 | in-del | -/AAGG | | | intron-variant | Eml1 | Mm_Celera | 12:108448109 | TGTGGGTTTTTTTTT[-/AAGG]TTTATTTTATTTTTA | 68519 |
| rs238578657 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108445744 | TTTTGTATGCAGAAA[A/G]TGATTTTTTAAAAAC | 68519 |
| rs238583990 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108430317 | GGAGACTTTTATTTG[-/TT]TTTTTTTTTTCCTAA | 68519 |
| rs238584088 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475546 | GCAAAGCTCACTTCT[C/T]ACCCTCCGTCGTGTG | 68519 |
| rs238594486 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108493608 | GATGGTCCCCCCAGG[C/G]GATGCTAGATCAATT | 68519 |
| rs238595668 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108510134 | ATTGTAGAAGTAAAG[G/T]GCACCTTTGTGTGGG | 68519 |
| rs238618174 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108428374 | AGTCTGACATGATAT[C/T]AACTCCTTCTCTGGT | 68519 |
| rs238651387 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108451597 | ACTCCGCAGTGACAC[A/G]GCTGGATGACGTGTA | 68519 |
| rs238672465 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108501279 | TCGTTCCTGTTGATG[A/G]GTGTATGGCTGGTTC | 68519 |
| rs238680967 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108427457 | TCTCCAAAGGTGAAT[C/T]AGACAGATGTAGCTG | 68519 |
| rs238694826 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108442480 | CTCAGCAGAAAAGTG[-/A]AAAAAATGTGCTTGC | 68519 |
| rs238696558 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108524350 | ATCAGATTACCATGG[A/C]CTAAGGCTGATCTTA | 68519 |
| rs238705256 | in-del | -/TGGGCCCTGATG | | | intron-variant | Eml1 | Mm_Celera | 12:108485247 | GTTTCTTCCTGGAAC[-/TGGGCCCTGATG]TCTTAGGGACCTCAG | 68519 |
| rs238733284 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406486 | ccactccacccaccc[C/T]gcacccctccccccc | 68519 |
| rs238737579 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524085 | TTCTCAGCACCTCAT[G/T]CGAGCTTCTCCAAAA | 68519 |
| rs238751681 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108424410 | TAGACTCATGGGAAT[C/G]TTTTTGCTCCCGGGT | 68519 |
| rs238775533 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108475125 | TAGGATCATCCATGG[G/T]TTATAACAACACAAA | 68519 |
| rs238796010 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443990 | TATTAAAGCATCGCA[C/T]CTTACTCTGTATGGT | 68519 |
| rs238799327 | in-del | -/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108374388 | CAGTAGCTGAGTGTG[-/T]GTGGGGACAGTAGCT | 68519 |
| rs238804307 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108398325 | CTGGGCCCGGCTGCC[C/G]TTTATCTGCCGAAGC | 68519 |
| rs238836501 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447044 | GAGTGGCAGAGCCAG[A/G]GTCCAGATGGGTATG | 68519 |
| rs238851117 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409390 | GAGCTGCTACGGAAT[A/G]GTCTTAGGCTGTCTC | 68519 |
| rs238862044 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108495186 | TGAGGCAAAGAATCC[C/T]GGTGTCTTTTGGCTT | 68519 |
| rs238862288 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108395983 | GCATCCCCTAAAATG[A/C]TCTTCTTGAGCCCCA | 68519 |
| rs238868763 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108529770 | TAAGGTAAATGGTTG[C/T]CAAAGATGCAAGAAA | 68519 |
| rs238914083 | in-del | -/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402024 | GGCGTGTTTTGTGTG[-/T]GTGTGTGTGTGTGTG | 68519 |
| rs238928226 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108465743 | TTTGAAAGACACTGA[A/G]AAATGAAAGGAAATC | 68519 |
| rs238930318 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474272 | GAGGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 68519 |
| rs238936491 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454155 | TAGATTACTTGTGAC[A/G]AGGAGTTCTGGTGTC | 68519 |
| rs238968603 | in-del | -/TA | | | intron-variant | Eml1 | Mm_Celera | 12:108508562 | AAAAAGTCTTCATTT[-/TA]AAAAAAATGTTCATA | 68519 |
| rs238984389 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108415505 | CTTCTGTCTTGTGCC[A/G]GCATCTGCATTCCTG | 68519 |
| rs238994164 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502516 | CAGAGCCAGGCCACT[-/G]GTACTCAGACAACAA | 68519 |
| rs239040858 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108371858 | GGGAGGAGATGCAGT[C/T]GGAATCCAGTTCCTA | 68519 |
| rs239041783 | in-del | -/ACACACACACAC | | | intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108537701 | TTCACCCTGACACTG[-/ACACACACACAC]ACACACACACACACA | 68519 |
| rs239043933 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460349 | TGAAAAACTTCAAAA[A/C]TAGAAGCATCCCTGG | 68519 |
| rs239061768 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108472842 | CACACCACACCTCAC[-/A]TATACCATACCACAC | 68519 |
| rs239122720 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418077 | TGTCTGTTTGATAGG[A/T]CTTCTATGACAAATG | 68519 |
| rs239123896 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443975 | AGCATGGAACATGCA[C/T]ATTAAAGCATCGCAT | 68519 |
| rs239134259 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464398 | GTGCATATCAGTGCC[C/T]TGACATTTACTTCTG | 68519 |
| rs239143500 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108401697 | AATTAAGGCTGGTAC[A/G]CCAGAGTGGGTGAGA | 68519 |
| rs239165333 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108450057 | GGCGGTTGAACTTGA[A/G]CAGCATCAATAACTT | 68519 |
| rs239195586 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507076 | AGGCAGGAGCTGATG[C/G]AGGGATATTTCTTAC | 68519 |
| rs239200642 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108486106 | ATGAGGGCCAAGCAG[-/C]CCCGCTCTGCTTGTA | 68519 |
| rs239201116 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429112 | TTAAATTGCATTTCT[A/T]TTTACGTGGTGTGTG | 68519 |
| rs239202453 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447105 | CATGGATCAGCATTG[C/T]CCAACCACTTAAGCA | 68519 |
| rs239228487 | in-del | -/AC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473355 | TACCACACCACCCAT[-/AC]ACACACACACACACA | 68519 |
| rs239241516 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108453576 | CAGGCTCCACCCATT[A/G]AGCCATGTCCCCAGC | 68519 |
| rs239241832 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446515 | ATGAGGCTGGCTGAC[C/T]GTGAGTTCAGGATCA | 68519 |
| rs239274214 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504834 | TATTAGAATACCGAA[A/G]TATTTTTGGGTCCTA | 68519 |
| rs239288825 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506237 | CTAACAGAGTGAGCC[A/G]GATTCTGAACCTTGT | 68519 |
| rs239296868 | in-del | -/TGT | | | intron-variant | Eml1 | Mm_Celera | 12:108516682 | TTGGATTCGCTCGGG[-/TGT]GGGGGGGGGGGGGGG | 68519 |
| rs239310255 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108382561 | GCTGGGATTGTAGGT[A/G]GGATTGTAGATGGGG | 68519 |
| rs239332334 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452459 | GCTGAGCCTTAGCTG[A/G]TGCAGCGCACACTCA | 68519 |
| rs239363851 | in-del | -/A | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402771 | TTCTCAGACTAGCAC[-/A]TGTCTCAATAATCTG | 68519 |
| rs239369631 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374510 | GGCTGCTCTGGATAC[A/T]CTCGTTGGGGGAGGG | 68519 |
| rs239373028 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108380630 | TGTCCTGGAGTTGGT[A/C]CCCACCTCGGAGATT | 68519 |
| rs239373760 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108375439 | GATGTCTCGAGTTAT[C/T]TCTATGTACCTTGAC | 68519 |
| rs239388869 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108511471 | ATCCAAACCCTTTCG[C/T]GATGATGGATCTGTT | 68519 |
| rs239391052 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108388855 | CTATACCATAAGAAC[A/G]CAGGGCTTGCCCATA | 68519 |
| rs239397937 | in-del | -/TTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108490145 | ATATTTACAAAGGGA[-/TTTT]TTTTTTTTTTTGAGA | 68519 |
| rs239398039 | in-del | -/GAATCACCT | | | intron-variant | Eml1 | Mm_Celera | 12:108521151 | GAGACTAAATCAGAA[-/GAATCACCT]GAGATTGAGGCCGGC | 68519 |
| rs239403659 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108419626 | CCTCCCCTCCTCCTC[C/T]CCCTCCTCCTCCCCC | 68519 |
| rs239411254 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422379 | CCATGGGGAGTAAGG[C/T]TCAGATCGTTAACCT | 68519 |
| rs239414444 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108521817 | TTTCCAGTCTTCTTA[C/T]AAAAACTCTTCTGGG | 68519 |
| rs239416310 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476727 | TAATATCTTTATCAC[A/G]GCAGGTTTAAACTCA | 68519 |
| rs239418848 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108390975 | cacacaacaccatac[A/G]cacacaaacacCCAT | 68519 |
| rs239419141 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469084 | TGGTCCCCAGAGCTC[C/T]AGAACATTGTGGACA | 68519 |
| rs239429760 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440361 | ATCAGGCTCAAGGAC[A/T]CGGAGACATTCAAGT | 68519 |
| rs239449174 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108485323 | GTTTTCCCTCCATGC[G/T]CTATGTTCTTTGAAG | 68519 |
| rs239463241 | in-del | -/TTA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108426493 | CAACCATTATTTTAT[-/TTA]TTTATTTATTTATTT | 68519 |
| rs239482471 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519194 | ACTGAACAACTGTGA[-/G]CTTCTTACAATACAG | 68519 |
| rs239498211 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108475132 | ATCCATGGTTTATAA[C/T]AACACAAAATGTCCT | 68519 |
| rs239502480 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476511 | TTTTAGACATTGTGT[A/G]AGACAAAGGCCCACC | 68519 |
| rs239521425 | in-del | -/CCCCC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473314 | TACACCAAGCATACA[-/CCCCC]CCCCCCCCCAAGCAC | 68519 |
| rs239531754 | in-del | -/ACTT | | | intron-variant | Eml1 | Mm_Celera | 12:108374303 | GGCCTTGGGCAAGAC[-/ACTT]ACCTGATGGGTGAAC | 68519 |
| rs239532297 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482312 | TTTCTTCAAGGGGAA[G/T]GAAGAGGGCAATGGA | 68519 |
| rs239541808 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379750 | AAATTCAGAGCTTTT[C/T]CTGCCTCTGCCTCCC | 68519 |
| rs239574437 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369445 | GACACGACATGGGCC[A/G]GGCCAGAGGAGCCTT | 68519 |
| rs239578251 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108429979 | TCCCTCCAGTGACTC[-/AG]AGTCTGCTCTATTTT | 68519 |
| rs239612302 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416889 | CACACTGCTAGAGAG[C/G]TTCTCATGTGTTAGG | 68519 |
| rs239619903 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108481721 | TGTCTCAATATCAGC[A/G]CCCCCTCTCCTCCCA | 68519 |
| rs239638630 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108461240 | CCTGTATTGTCTCCT[C/G]CAGGGGATCCAACAC | 68519 |
| rs239658682 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108449864 | CTACCCACGTAGCCG[-/C]CATCTCGCTAGCCAG | 68519 |
| rs239668675 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507846 | TTAGTATTTGAGATG[A/G]TGGAATCATATTCAT | 68519 |
| rs239679311 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108425537 | ACTGTTTCCTGTTGT[C/T]CCCCGGGTACTTGGT | 68519 |
| rs239682478 | in-del | -/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406518 | GTCTCCTTTCTAATC[-/T]TTGTGGATTTGCCTG | 68519 |
| rs239700476 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421206 | TACATTGTCTCTCCA[C/T]AATGCTGCAGGTCCC | 68519 |
| rs239703795 | in-del | -/CTT | | | intron-variant | Eml1 | Mm_Celera | 12:108532043 | CTGGAACTCACTAAC[-/CTT]CTTCTGACTTAAACC | 68519 |
| rs239706603 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108515858 | GTGTGCCACCACGCC[C/T]GGCTAAACCTGCATT | 68519 |
| rs239709727 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108470747 | TGAGAGACTGTCTTG[A/G]TTGTCAGTTGATGAA | 68519 |
| rs239732047 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455433 | ACAGTGCATAGCTAG[C/T]TTTGTTTTATTATAA | 68519 |
| rs239735994 | snp | C/T | | | synonymous-codon | Eml1 | GRCm38.p3 | 12:108521707 | GCCTCAGTTCCTGAC[C/T]TGTGGACATGACAAA | 68519 |
| rs239749188 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108477934 | GTATAGAGATGCCTC[A/G]GGATTGTGAAAGCTT | 68519 |
| rs239750516 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108467132 | CCCAAGGACCTTTTC[C/T]AGGGCCCACAAAATA | 68519 |
| rs239764463 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108395372 | AAGCACAAGGGAGGG[C/T]CCATGCTAGGATCCA | 68519 |
| rs239766721 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383045 | TAAAAGGATTTACTG[C/T]TAGAGTTCCTTTCTC | 68519 |
| rs239783144 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108487902 | CAACCCCCCCCCCCC[-/G]ATTTGTGACCAGAGA | 68519 |
| rs239790316 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108515311 | TGAGCTGTTGGAGTT[A/C]CGAACAGGACAACCA | 68519 |
| rs239805780 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478519 | ATGTGGTTGCTGGGA[A/T]TTGAACTCAGGACCT | 68519 |
| rs239810947 | in-del | -/A | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477464 | AAAACTAGCCAGCAC[-/A]AGTTACCTTTAAAGT | 68519 |
| rs239811827 | in-del | -/GAAAGA | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412793 | TACAGAGAAACTATC[-/GAAAGA]GAGAGAGAGAGAGAG | 68519 |
| rs239823720 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108526540 | CAGGATATCTGACAC[A/C]TTTTTCTGATCTCTG | 68519 |
| rs239827703 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108382200 | TTCTTGCAAGAGAAG[A/G]GCCATTTTAAAGTAC | 68519 |
| rs239828938 | snp | A/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402592 | AGGCGAGCACTCTGC[A/T]AACTGAGCCACATCC | 68519 |
| rs239854692 | in-del | -/AGGTCTTAATTCCCATTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108451894 | AAAGAGAGGAGCTGA[-/AGGTCTTAATTCCCATTGT]AGGTTTGGGTATCAG | 68519 |
| rs239859528 | in-del | -/CACACACACA | | | intron-variant | Eml1 | Mm_Celera | 12:108388349 | TGCCCTCACCTCCAC[-/CACACACACA]CACACACACACACAC | 68519 |
| rs239893127 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402124 | CACCTCAAACTCACC[G/T]GCCTCTGCCTCCCGA | 68519 |
| rs239893858 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108394398 | AAATTTTTAATTTAC[C/T]GTATGGTATGTGTGT | 68519 |
| rs239896175 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108478126 | GCTGTAAAACTCAGG[A/G]TGAAAGCTACAGTGA | 68519 |
| rs239925302 | in-del | -/TGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108458417 | CCAGTCACCCAGGAC[-/TGTG]TGTGCATCGCACAGG | 68519 |
| rs239930073 | snp | A/C | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369463 | CCAGAGGAGCCTTTG[A/C]AGTTTTGAATTCCTT | 68519 |
| rs239939025 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108485062 | TAGATTTGTCAAAAG[C/T]CAGCACGTTAGGCGG | 68519 |
| rs239940796 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503653 | ATAGTTAAAATATTG[C/T]TTTGTCCTAGTCAGC | 68519 |
| rs239944110 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421073 | CCAGGTAGGGGACAG[C/T]GAGGACTCTTGACTG | 68519 |
| rs239947908 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108500397 | GTTCTGACTGGGGAG[A/G]CTGGCTAATCGTCTA | 68519 |
| rs239950090 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108507176 | TCCACCCACAATGGG[C/T]TAGGCCCTCCCTCCT | 68519 |
| rs239975011 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108391289 | GCTCCTCCATCCTCC[A/G]TGCCCCTCAGTGATA | 68519 |
| rs239992210 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379806 | CACCACTCTTCAAGG[G/T]TCTTTTTAATTTAAT | 68519 |
| rs239995153 | in-del | -/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404974 | TGTGCACGCGTACAA[-/C]ACACAAACTTCTACA | 68519 |
| rs240022104 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108513377 | GTCAATGCTTGAGGC[A/T]TGCTCAAGACCAGCC | 68519 |
| rs240025985 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108484649 | GGGCCTCCCACTGCC[A/T]CAGAGCCCTTTCAGC | 68519 |
| rs240035648 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474420 | TGGGACCTTCGGAAA[A/G]ATCTCAACCTTTTGG | 68519 |
| rs240039825 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506834 | TGTACAGATGGATGG[A/G]TTGGGGGCCAGGGGA | 68519 |
| rs240045206 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108469171 | TCCTGACTGGAGCAG[C/T]GCTGGAGCAAGCACA | 68519 |
| rs240048658 | in-del | -/AGACAGAC | | | intron-variant | Eml1 | Mm_Celera | 12:108391015 | ATACAAACACTACAT[-/AGACAGAC]AGACTGATAGGCACA | 68519 |
| rs240057928 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376468 | TGTGGTTGCTGGGAT[C/T]TGAACTCAGGACCTT | 68519 |
| rs240058743 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108435437 | ACTTCAGAGCCCACT[A/G]CACACCATGGGGACC | 68519 |
| rs240060585 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108428561 | GTACCGCACTCACTG[C/G]CAGTTAGCTTGGAGG | 68519 |
| rs240062769 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388905 | GAGAGCTGGTCTCTC[C/T]TCTTTCCTAATGCTG | 68519 |
| rs240066372 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108526238 | CCCGGCTGTGAATGC[A/G]TCGTACAATACACAC | 68519 |
| rs240072403 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519952 | CAAGCTTCATCCTTG[A/C]TTTTTGTGATGTAGA | 68519 |
| rs240109629 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108470361 | CTTAATGAGACCCAC[A/G]TTGTCAATCCTCCCC | 68519 |
| rs240112180 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108500541 | CATCCTAGGGTGTAT[A/G]CTCACTTTGATCGTT | 68519 |
| rs240122433 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108531391 | CTTGTGTGGTTGTGC[A/G]CATCTGTAGTCCCAG | 68519 |
| rs240126772 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108434782 | ACATAACACATACCT[C/T]ATATCATACACACTT | 68519 |
| rs240130569 | in-del | -/AAAAAAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108415365 | TGTGATGGCATAGTT[-/AAAAAAAA]AAAAAAAAAAAAAAA | 68519 |
| rs240160508 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530809 | ACCGCTTGGAAGGAC[C/T]ACTCTGCTACCTTCA | 68519 |
| rs240160885 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473568 | CCCAGCCATGCCATC[C/T]GGGTGCAGGCCGTGC | 68519 |
| rs240174858 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108507524 | AACCAACCACTTGTT[C/T]TTTTGAAACAGGGTC | 68519 |
| rs240178702 | in-del | -/GT | | | intron-variant | Eml1 | Mm_Celera | 12:108429952 | CTCCAAGCCTCGCGC[-/GT]TCTGAAGGCGTTCCC | 68519 |
| rs240178860 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390148 | GAACCTGTGTGAAAA[G/T]CTGGGCTTGGAGATG | 68519 |
| rs240182341 | in-del | -/TGGCTCCA | | | intron-variant | Eml1 | Mm_Celera | 12:108495208 | TTTTGGCTTCCTGTC[-/TGGCTCCA]GCATCCCGTTCCTAT | 68519 |
| rs240221896 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108435261 | TCAGCATCTCACTTA[A/G]CATCTCTGAGCTTCC | 68519 |
| rs240222464 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108386344 | TTATTGGGCAATATT[G/T]GGCCTCAAGCCTCAG | 68519 |
| rs240248272 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404991 | CACAAACTTCTACAG[C/T]ATCCTAGGTGATTAA | 68519 |
| rs240250928 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480372 | CCTCCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCT | 68519 |
| rs240258901 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437551 | TGAGACCAGGACTGT[A/G]TGCGGCACGCTCAGG | 68519 |
| rs240262687 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447393 | GATGCCTTGGCCTGC[C/T]TGGCAGGCTTGGAGA | 68519 |
| rs240270949 | in-del | -/GAAC | | | intron-variant | Eml1 | Mm_Celera | 12:108479060 | CTGTTTTGCAGGTAT[-/GAAC]GTGTGTGTGTGTGTG | 68519 |
| rs240278104 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108503698 | AGATAAGGAAGCGTC[A/G]GGCACACGCATTCTT | 68519 |
| rs240309268 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404790 | CAAATACATACACAC[A/G]CACATGAACACACAC | 68519 |
| rs240310513 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108393166 | TGTTACATCTCAAAT[C/T]CTACAGGTAGTGTGT | 68519 |
| rs240342153 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108442908 | CAGTAAACCCTGAGG[A/C]ATGTTACCAAGGTGC | 68519 |
| rs240351395 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108535483 | CTTTCTCATGATCCA[C/T]AGTAGTATTTTCTGA | 68519 |
| rs240357984 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403149 | CCATTAACCAACCAC[C/T]CGTCCCCTCCAACAC | 68519 |
| rs240358358 | snp | A/G | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411581 | ATGGGCATGGGTCCT[A/G]CTTGTTTGGGAGGCA | 68519 |
| rs240366724 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433230 | TCTGACCGAGTCAGA[C/T]GTCTCCAGCACTCTC | 68519 |
| rs240368174 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503104 | GTTCCCTTGTCCCCT[C/T]GGGGGCCAGGGTAGC | 68519 |
| rs240368316 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108510359 | CAGCATTTGAGAACC[A/T]TTGGGTCCTCACCAG | 68519 |
| rs240386772 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402634 | TAGTTTATTAAGGTG[A/G]TAAAATACGTAGCCG | 68519 |
| rs240395333 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108533703 | CACATGCTTCATGGA[C/T]AGGGATGGCTGGTCA | 68519 |
| rs240408085 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108509702 | TGAGTTCGAGGCCAG[A/C]CTGGTCTACAGAGTG | 68519 |
| rs240448765 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392969 | GCAGCCGAAGGGAGG[C/T]ATGAATAATATAGAA | 68519 |
| rs240469630 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438033 | GACTATCCCCACTAC[C/T]CTGCATGATCCCTTG | 68519 |
| rs240524473 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108524860 | AACGAAATATATCTT[A/C]AAATAATTATTCTGT | 68519 |
| rs240525912 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532829 | CTTTGTCTGCATTAC[A/G]TAATTTGTTAGCACT | 68519 |
| rs240528513 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108384530 | ACATGTGCCCTGCCC[A/T]GAGACAGCCCTTCTC | 68519 |
| rs240530133 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378335 | TGACGGCACTGAAAG[C/T]CCACGCATGCTCAGT | 68519 |
| rs240535140 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437678 | CGTCAGCTGGCCTGA[C/T]TTGTCCATGTTCCCA | 68519 |
| rs240561642 | in-del | -/CACACA | | | intron-variant | Eml1 | Mm_Celera | 12:108475477 | TCATGTGTGCAGCAC[-/CACACA]CACACACATACCAAC | 68519 |
| rs240581740 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402672 | AACTATAAGCTTTTC[C/T]TTCCGACCACTTTGT | 68519 |
| rs240587870 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108497745 | AAGTGACCCCACAGG[A/G]GTGGCATATTCAAAT | 68519 |
| rs240596489 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108443095 | GGAGGGTCTCCGTGA[A/G]TTTGAGGCCAGCCCG | 68519 |
| rs240599612 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455085 | GCATGTGTGTGTGTG[C/T]GTGTGTGTGTATGTG | 68519 |
| rs240639056 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504592 | CCTGTGGGGTTTGGC[A/G]CAGGTTTTGCTGGTC | 68519 |
| rs240662229 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442658 | GGACCTCTAGAAGAG[C/T]AGTCAGTGCTCTTAA | 68519 |
| rs240669043 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108389587 | TTTAGGGTTTGGTAT[A/G]TGAGGTATGGGGTGC | 68519 |
| rs240699886 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406515 | CCAGTCTCCTTTCTA[A/G]TCTTTGTGGATTTGC | 68519 |
| rs240731219 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108450233 | GGTGTTAGGAAAGTG[-/T]TTTTTTGACCTCCTA | 68519 |
| rs240733472 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108454080 | CAGACAACCTGGTGC[A/G]CAGAAATGAAAAACT | 68519 |
| rs240733814 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108502917 | GATATAGCTAAACAC[-/A]AAAAAAAGTTACAAA | 68519 |
| rs240743721 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108430635 | ACTCCCTGTAATCCC[A/G]GTGGAAGGTAGGGCA | 68519 |
| rs240757800 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108374133 | AGGAGGAGCTGGCAG[A/G]CCTCTGGGCTGTCAG | 68519 |
| rs240759332 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108414768 | GGATCCCCGTCTCCA[C/T]ATCACTCTAGACTGC | 68519 |
| rs240760574 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108527309 | TTGCAGTTTATCTAG[G/T]AGCATCTCTGTGGCT | 68519 |
| rs240763150 | in-del | -/GTTAA | | | intron-variant | Eml1 | Mm_Celera | 12:108486229 | TTGACCTTGGTTAAG[-/GTTAA]GGATTAAGGAAGGTG | 68519 |
| rs240763888 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108396721 | CAGCCAGTGCCTGTG[C/T]TAGGGAGAGGCGCCA | 68519 |
| rs240799632 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108458501 | AGAATGTCTTGTGTC[-/T]CCTTTTCCTGTTAGG | 68519 |
| rs240803450 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436959 | AAGCAAAAGCTGCGC[A/G]TGCTTTGAAGCAATA | 68519 |
| rs240819731 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108414106 | ATATTTTCCTTATGG[A/G]AGATTTATTATGGGG | 68519 |
| rs240866326 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475842 | TTTTCCATGTGGGTC[C/T]CTAGGATGGAACTCC | 68519 |
| rs240867364 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108452114 | TTCGCTTCTCCTGCA[C/T]GCCGTCTTTTATCAT | 68519 |
| rs240868829 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436301 | TGTGGAGTGGGATAA[A/G]CACCCATGTGTTCCA | 68519 |
| rs240883082 | in-del | -/AC | | | intron-variant | Eml1 | Mm_Celera | 12:108390800 | CATACAGATACATAT[-/AC]ACACACACACCAGAC | 68519 |
| rs240886416 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532845 | TAATTTGTTAGCACT[C/G]ACATGTACAGCATTT | 68519 |
| rs240898742 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502045 | GGTAAGACACATCGT[A/G]TGGCTGAGAATGTGA | 68519 |
| rs240902703 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108468093 | GTCTTCTGTATATCC[-/TG]GGGTCCTGACGAAGT | 68519 |
| rs240905085 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432733 | GCAGACCAGGCCAAA[A/G]GATCTGGAGCCTCAA | 68519 |
| rs240909867 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108399871 | CAACAGTCACAGCCC[C/T]AAATCCAAGCTCCCC | 68519 |
| rs240936016 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108388474 | AGCTGCAGCTTCCCT[-/G]GGGGGCTATGGCCAG | 68519 |
| rs240937396 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108414207 | ATTGGTTATCACAGA[-/C]TTTAGAGTTTTGTGT | 68519 |
| rs240959160 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108456911 | CTGGTGGATTCTCCA[G/T]ATAAGTCGGGAGACA | 68519 |
| rs241001343 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484561 | ACTGCACTGCAAGAG[C/T]GTTTTATGCAACTCT | 68519 |
| rs241035343 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108534602 | CAGCCTTTCCTCTTA[A/C]GACAAGTGATGTCAC | 68519 |
| rs241036269 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108462877 | CTTTGTCCTTCAAAG[A/C]GTGGGACCATGTTTC | 68519 |
| rs241036332 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455970 | TGGAATTAACATTTC[C/T]GGTGGACACCGTCAT | 68519 |
| rs241074359 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433627 | CTCTGGAGTGGCTTC[A/G]CAAGCACACCACACC | 68519 |
| rs241077197 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108477763 | ACTTTTGTGTGTTGA[-/TT]TTTTTTAGATCTTGA | 68519 |
| rs241082454 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370177 | AGAGTGGGGACAACC[A/G]GAGTGAGCAGGCTTG | 68519 |
| rs241084021 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451232 | CCTGGGAGGAAAAGT[A/G]GAAGCAAGGAAATCC | 68519 |
| rs241112506 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442105 | ACCTGCCACACAGGG[C/T]CCGCCAGAACCGGAC | 68519 |
| rs241163823 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488135 | GTGTGGGAGTGATCC[C/T]GTGGGAGCCTTCTGA | 68519 |
| rs241173164 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108447528 | CCTTCTTATGATCTA[A/G]AAGATCATCACTTCG | 68519 |
| rs241173739 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108439882 | CTTAAAAAAAAAAAA[A/G]AAAAAAAAATTCCAG | 68519 |
| rs241201909 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535592 | AGAAAGTTCAGATGC[C/G]AGTGGGGGGCAGAAA | 68519 |
| rs241221179 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108495621 | AGTGAGCTGGCTGAC[A/G]GGTCACATTCCTAAA | 68519 |
| rs241222479 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496155 | GGGCACAGAACAGCA[A/G]TTACAGGCTGGAAAC | 68519 |
| rs241224941 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108439132 | ATCTATAGAACCTCG[A/C]CGAATCCTCTCTTCC | 68519 |
| rs241258600 | snp | A/C | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402533 | GTCAGGCACCACACC[A/C]AGTTTATGTGGTGTT | 68519 |
| rs241272664 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108478852 | ACTGTGTTGGATACA[A/G]TGGGCTTGGCTGATC | 68519 |
| rs241294053 | in-del | -/CT | | | intron-variant | Eml1 | Mm_Celera | 12:108444386 | ACCATCATAGGTGTA[-/CT]CTCAGGCACAGGGGT | 68519 |
| rs241299737 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108394356 | CTTTATTTGGACACT[-/A]AAAATATTGGACACT | 68519 |
| rs241301550 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108459782 | AACAGACAAGCTACC[C/T]TTTATGCCATTTTCA | 68519 |
| rs241313805 | snp | A/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384462 | CCCTCCCTCCAGGGC[A/G/T]CACAAGTCGTTACAG | 68519 |
| rs241326291 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108384295 | CCTGAGCCAGGACCA[A/G]GGAGGTACCCCCAAA | 68519 |
| rs241333778 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480402 | TTCCCCGTTTTTGTA[A/G]TATTGGCAATTTTTG | 68519 |
| rs241355644 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445164 | TAATTCCAGTTGGGG[-/T]GTGTGTGTGTGTCAG | 68519 |
| rs241361826 | snp | A/C | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536450 | TTTTGCTTTTGTGAA[A/C]CTGCAGTGCCTGTGG | 68519 |
| rs241363299 | in-del | -/A | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507444 | GAGAAACCCTGTCTC[-/A]AAAAACCAAAACCAG | 68519 |
| rs241369137 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108487571 | ATAAACAAAAATAAA[A/C]ATAGTACTTAAGTTG | 68519 |
| rs241370488 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108479880 | CTCTGTTCCTCTGTT[A/C]ATTTTGCTAGAGGTG | 68519 |
| rs241382274 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108395690 | TATGAGATTCATATG[-/T]TTTTCTAGGTCATTA | 68519 |
| rs241382784 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108459176 | TAGTTTCATCTCCCC[A/T]GCTGGGTATTACAGA | 68519 |
| rs241399481 | in-del | -/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403222 | TTGTTTTTTTTGTTT[-/G]TTTGTTTTGTTTTGT | 68519 |
| rs241411474 | in-del | -/CCTG | | | intron-variant | Eml1 | Mm_Celera | 12:108469157 | CCCGGCCCCTCCCCT[-/CCTG]ACTGGAGCAGTGCTG | 68519 |
| rs241416817 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108432618 | AACAGTACCTGGGCT[-/A]TGCGGCTCCTCTAAG | 68519 |
| rs241419618 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108464785 | ACAGGTTATGGTTCT[A/G]GTGCTAGAGAAGATG | 68519 |
| rs241429673 | in-del | -/A | | | intron-variant | Eml1 | GRCm38.p3 | 12:108398420 | AGAGGTTGGGCAAGG[-/A]CATGATAGGGAGGCT | 68519 |
| rs241434568 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486595 | AGTTTCAGTGGGGGA[A/G]TTTGGAGGATGGGAA | 68519 |
| rs241451563 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372589 | GCCACCCGTAGGTAG[A/T]GTATTTCAGGAAGGC | 68519 |
| rs241506303 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419270 | ATCATACTCCAGCCC[A/G]TGATAGCTCACATTT | 68519 |
| rs241507747 | in-del | -/CCTCTCCCTCCT | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407938 | CCCTTTCTTGGATCA[-/CCTCTCCCTCCT]CCTCTCCCTCCTCCT | 68519 |
| rs241510030 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108465347 | CTGACTTCTGAGGGC[A/G]GAACTACATCAGAGG | 68519 |
| rs241512681 | in-del | -/AAAAAAG | | | intron-variant | Eml1 | Mm_Celera | 12:108509579 | GGGCGCAGTAATTTA[-/AAAAAAG]AAAAAGAAAAATTTA | 68519 |
| rs241530693 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108516999 | TTTCACCACCTGAGA[C/T]CTAGACAGCAGCCTG | 68519 |
| rs241531715 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108452403 | GATGAGGAGGAAGTT[C/T]CTGGGCCTCACTACC | 68519 |
| rs241536231 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108465819 | CTACGTCATGGGGAG[G/T]GGGCGGAGCTAGGCA | 68519 |
| rs241565077 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108451894 | GAAAGAGAGGAGCTG[A/T]AGGTTTGGGTATCAG | 68519 |
| rs241568126 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108379684 | ATTATTTATTTTTTT[-/AG]TTTTTGTGACAGGGT | 68519 |
| rs241572850 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475401 | CAGCCCCTGACACGA[C/T]CCCTTTTCCCTCTGA | 68519 |
| rs241583355 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108428954 | AGACCAGCCTGGCCT[C/T]GAACTCAGAGATCTG | 68519 |
| rs241590925 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108394152 | AGCCAGGTGTAATAC[-/T]TATCTTAGTTTCAAC | 68519 |
| rs241606730 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457854 | GATGTTGCTTTGATG[C/T]CTGTGTTCCTGTGTT | 68519 |
| rs241622567 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108472891 | ATACCCCCAGACATA[C/T]ACAAAAGCATACCCA | 68519 |
| rs241633139 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108518835 | GGATTAAAGGCATTC[A/G]CCACCACTGCTCAGC | 68519 |
| rs241635220 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108510533 | GGCAGGTCTGTGGGC[C/T]CTGTAACAGGACACT | 68519 |
| rs241638601 | in-del | -/A/AA/AAAAAAAAA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108493964 | GCCCTGAACTGATTT[-/A/AA/AAAAAAAAA]AAAAAAAAATGGCGC | 68519 |
| rs241644538 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108507230 | TTACAGCTGGAAATC[A/T]CGGAGGCATTTCCTC | 68519 |
| rs241652980 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108458532 | TCTCAGAGCATAAAA[A/G]TACTTTTCTGCAGAC | 68519 |
| rs241688623 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108385713 | GTAATCTTAGCATTC[A/G]GGAGTTCGGGATAAT | 68519 |
| rs241699760 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108438913 | CAGGAGCTGTCAGAC[A/T]GAGAGGAAAGGAGGG | 68519 |
| rs241737870 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108482884 | TGAAAGAGATCACAG[C/T]TTTTAATTCATCCTC | 68519 |
| rs241739794 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108491535 | TATGCTTTCTATCTC[G/T]TTGCTCCCTGTCCCA | 68519 |
| rs241763614 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412970 | TTTTGAGAATATTTA[-/T]TTTTTTTCTGCTGCT | 68519 |
| rs241765738 | in-del | -/TGTGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108519413 | GAGTTTGTATGTTTA[-/TGTGTG]TGTGTGTGTGTGCAC | 68519 |
| rs241767159 | snp | C/T | | | intron-variant, missense | Eml1, Gm33385 | Mm_Celera | 12:108401333 | ACAGGCTTTGAGCTC[C/T]GAGTCATCACGTGGC | 68519 |
| rs241814322 | in-del | -/CGCG | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404747 | GTGCAAATACACACA[-/CGCG]CACATGAACACACAC | 68519 |
| rs241823414 | in-del | -/GTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108425964 | CACATATGGGTGCAG[-/GTGT]GTGTGTGTGTGTGTG | 68519 |
| rs241846210 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108490196 | TTTTGATTTGGAAAC[A/G]AGAGAATGGGAATGC | 68519 |
| rs241874127 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108505675 | TACTGATGTATGATA[C/T]TCACTTGGACTTGGT | 68519 |
| rs241888099 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108445408 | AGCATCTTCGTCCTT[-/G]GGGGCTGGACATGTT | 68519 |
| rs241896689 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108389921 | AAGGCAATTGTCTCT[A/G]TCCTCCCTATCCCCA | 68519 |
| rs241897912 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455331 | CTCAGAAGCAGACCA[A/G]GGTTCCTTTCTGTTC | 68519 |
| rs241920998 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496335 | AGCAAATTCTGCTGT[C/G]TTTTTCAGCCAGGCT | 68519 |
| rs241932148 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108487789 | CTGCCATGACGTCTG[C/T]GTTTGTCCCTGGTCT | 68519 |
| rs241933259 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405753 | GGATCACAGGCACAC[A/G]GCATCATAGTTTTAA | 68519 |
| rs241934644 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108461857 | TAAGTGAAGCAGATA[C/T]AGAACCCATCGACTG | 68519 |
| rs241987902 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108454850 | CCTCGTTTTCTGAGC[A/C]TGTTCTGTAGAGTCC | 68519 |
| rs242010973 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108485265 | CCCTGATGTCTTAGG[-/AT]GACCTCAGCTCCTGT | 68519 |
| rs242017642 | in-del | -/CTGTAA | | | intron-variant | Eml1 | Mm_Celera | 12:108439188 | TGCTGAGCCAGCACT[-/CTGTAA]CTGTGTTCCAGCCCC | 68519 |
| rs242030644 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108461288 | CCACACACTGACATG[G/T]AATTAAAAGTAGAAC | 68519 |
| rs242040073 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108416149 | AGAGAGAGAGAGGGT[C/T]GTCATCCCCCTCCCC | 68519 |
| rs242067675 | snp | G/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421899 | TCAGGTCAGAGCTCC[G/T]AGCCTGATAGCAGGC | 68519 |
| rs242102731 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108415360 | TCTCAATGTGATGGC[A/T]TAGTTAAAAAAAAAA | 68519 |
| rs242104406 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108468223 | CCCAGAAGGTATGGC[C/T]GACTAACAGTGGATA | 68519 |
| rs242104608 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108423693 | CCTCCAGAATCCTTT[G/T]GGGGTCACTTGGATG | 68519 |
| rs242113619 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408855 | AATCTCAGAGCTTTG[A/G]CCAGTTGTGGATCTC | 68519 |
| rs242129833 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108520732 | TGGCCTCAAACTCAC[A/G]GAAATCTGCCTGCCT | 68519 |
| rs242149057 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108506742 | AGAGGCAGCTTCAGA[A/G]CAAGTTCCCATGATT | 68519 |
| rs242149312 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108443380 | ACTCTCACTGAGTCC[-/G]TCGCTTCTCCTCCAG | 68519 |
| rs242157435 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417566 | TGGAAGCTTCAGGCA[C/T]GTCGCAGGCAGACAG | 68519 |
| rs242158301 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422333 | CTCTCTAGCTTTCTC[A/G]ATTGTCACTTGGCAT | 68519 |
| rs242177713 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408226 | AGTGCTGGGATTAGG[C/T]GTGTGCCGCCACACC | 68519 |
| rs242186543 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108377528 | TATGAATGAATTCTC[A/C]TTGCTTGAACCCTGC | 68519 |
| rs242209588 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108534580 | ATGAATTGGTCTGAC[A/T]CTGCCCCAGCCTTTC | 68519 |
| rs242209941 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108528403 | TCATGTTCAGACTCA[A/G]CCTCCTCTCACCAGC | 68519 |
| rs242209951 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519783 | ACTCACTCTGTAGAC[A/C]AGGCTGGCAGATCTG | 68519 |
| rs242231202 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108514246 | AACAAAGAAGAAAAC[A/T]GGCAGCAGCCAGAAT | 68519 |
| rs242232303 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506024 | TTGGAGTATTGTGAG[C/T]CATCTGTCACGGGTG | 68519 |
| rs242237077 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408127 | GTTCCCTTTTTGGGG[A/G]TGGGGGCTATTTTTT | 68519 |
| rs242245749 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527829 | GAGTTGCAGGGAGCA[A/G]TTAGACGGCTGAGCC | 68519 |
| rs242248472 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471128 | GCACACACAAGCCCC[A/G]GGTTTGATCCGCACG | 68519 |
| rs242261230 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108490529 | GGCTAATACAGAGAA[A/G]AGCCTAGGGACCCCC | 68519 |
| rs242267566 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108513586 | GCATCTGTCGGCCTC[C/G]GTTAACCTGACTTAT | 68519 |
| rs242274963 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108451551 | AGGAAACCTTTGGGG[A/G]TGGTTCAGATGTGCT | 68519 |
| rs242276217 | in-del | -/CG | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404870 | ATGAACACACACACA[-/CG]TGCACATGCAAATAC | 68519 |
| rs242281389 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522308 | AGGATCACAGGAAGG[A/G]CAGGCTCCAGTAAGA | 68519 |
| rs242284381 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455841 | CAGACTCTGAGCCTG[C/T]CATGTTGCTTGCTCC | 68519 |
| rs242290986 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393556 | AGGGAGTGGCGCTGT[A/G]CTGGGGACACCTCGG | 68519 |
| rs242328762 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108505934 | AATTTTTATTTACAT[A/G]TATGTGTCTCTGTGT | 68519 |
| rs242331514 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381074 | GGGTCGGGGCTCAGG[A/G]AGTGGGGCCGGGCTC | 68519 |
| rs242348864 | in-del | -/A | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473159 | AGCGTAGACACACAC[-/A]ACATACCATACCATA | 68519 |
| rs242373938 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108513439 | AGCACCCCTGAGGTC[A/G]GGACTCTGCCTCAAG | 68519 |
| rs242379380 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471109 | TTGGTTGAGTGCTTA[A/G]GTAGCACACACAAGC | 68519 |
| rs242393920 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108519582 | AGCCCCGCCCCTGGG[A/T]ACGGCCCACTTCCTT | 68519 |
| rs242394041 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108380690 | TGGGACATAACCCCT[C/T]CTACTCGGCTGTTTA | 68519 |
| rs242411736 | in-del | -/CA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473373 | CACACACACACACAC[-/CA]CACAAAGAATACAGC | 68519 |
| rs242412647 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470690 | AGAGGACAGCTTCAG[A/T]TGAGGAATTGTCTAG | 68519 |
| rs242440292 | in-del | -/TTT | | | intron-variant | Eml1 | Mm_Celera | 12:108443664 | ACTGCCACCCGTCCC[-/TTT]TTTTTTTTTGAAAAT | 68519 |
| rs242466824 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108440069 | GAAGGGCCCAGAGAG[A/G]CTGAGAGACCAGAGT | 68519 |
| rs242475951 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108485431 | CACATGCACACACAC[-/AT]ACACACACACACACA | 68519 |
| rs242494188 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477506 | TTGCACTGAATCTAT[A/G]GAGTGCTTTAAATAA | 68519 |
| rs242496604 | in-del | -/AGAG | | | intron-variant | Eml1 | Mm_Celera | 12:108484534 | CCATAGCGGGATAAT[-/AGAG]AGATGCTCCTTACTG | 68519 |
| rs242503227 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108380640 | TTGGTCCCCACCTCG[G/T]AGATTGTTTCCTTTG | 68519 |
| rs242523967 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108439454 | AGATTTATTTATAAA[A/T]AAGTACACTATAGCT | 68519 |
| rs242538912 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108444631 | GCCTGGACAGCTGGG[A/G]GCATTGTCTTGCTGT | 68519 |
| rs242563981 | snp | G/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108411935 | GGGGAGGGGGAGTTG[G/T]GTTTTTTTTTTTTTT | 68519 |
| rs242564086 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108419449 | ACTACATATATGTGG[A/C]TATACATGATGCTAA | 68519 |
| rs242568930 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108386422 | TTATGGAGTGCCCAG[A/T]TCCTGGCCCCGGATG | 68519 |
| rs242577194 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108426756 | CCATTAGCAATTAGT[-/A]CCCTAGCCCCTGACA | 68519 |
| rs242586644 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108444480 | AGGGATATAAACTCT[A/G]TTGCATTTACTCACC | 68519 |
| rs242593967 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108502364 | TAAATAAATAAATAC[-/TT]TTTTTTTTTGGTTTA | 68519 |
| rs242608863 | in-del | -/TA | | | intron-variant | Eml1 | Mm_Celera | 12:108377901 | TAGGCTCTGTATTTT[-/TA]TTTTTTTCACTGTGT | 68519 |
| rs242612262 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108517232 | GGGCAGCAGGACATT[A/G]TGGTTCTCCTGGTTA | 68519 |
| rs242625531 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482810 | GTCCCCTTGGGCCCC[A/G]GGCCCTGTTTATAGC | 68519 |
| rs242641221 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443906 | TAGCGTGTTTCAAGA[C/T]GCTAACACTTTGAGT | 68519 |
| rs242647727 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108516753 | CATAGAGGCAGTTTA[A/T]TTACAAGTAAAATAA | 68519 |
| rs242668265 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412615 | AGGTGCTGGGATGGC[-/AAG]AAGAATTATGGATGA | 68519 |
| rs242692777 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108453174 | CATTATGTGTATATC[-/TG]TGTGTACATGTGTGT | 68519 |
| rs242696821 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108384258 | GAGCACAACACAAAG[A/G]TAAATGCATCACTTC | 68519 |
| rs242724326 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524369 | AGGCTGATCTTAAAT[A/T]CCAACAAAAACAACA | 68519 |
| rs242750268 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474415 | GCCTGTGGGACCTTC[A/G]GAAAGATCTCAACCT | 68519 |
| rs242754389 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383470 | TTTTTAGTGTAATTA[C/T]GAAAGATTATTCTAT | 68519 |
| rs242755132 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108379428 | CTCTCCCATGAAACC[A/G]TCTCTCTGGTCTCTT | 68519 |
| rs242762257 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524107 | TCTCCAAAATTGATT[A/G]TATAGCCGGGTGGTG | 68519 |
| rs242768630 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460224 | CGAGAGTATTCCTAA[C/T]CTGAAAATTCAAAGT | 68519 |
| rs242772161 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108429470 | CACCTGGACACTGAG[A/G]CATCTCCAAGCCCGT | 68519 |
| rs242775860 | snp | C/T | | | intron-variant, synonymous-codon | Eml1, Gm33385 | Mm_Celera | 12:108411024 | GGAGACAAGGAAGGG[C/T]TTGGTCAGAAGAGCC | 68519 |
| rs242787847 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474175 | CTTCATTTTGATTGT[A/G]TCAAGTTGATAATTA | 68519 |
| rs242814178 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460497 | AACATTCATTCTCAT[A/G]AGAACACCAGGGGCA | 68519 |
| rs242814288 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108467359 | GCCCCGGGCATTGAA[C/T]CCGTAGACATGGAGG | 68519 |
| rs242821689 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376228 | TTCAACAGCTTTCTT[C/T]TCCTCCTCCTCCTCC | 68519 |
| rs242826202 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458581 | TTAAATGTTATGGGA[C/T]GGTTTTCTGAAGATT | 68519 |
| rs242841433 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474207 | AACTCACCATCAGCC[A/G]GGCATGGTGGTGCAC | 68519 |
| rs242846756 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108442293 | TAGCGCACAGCTCCA[A/C]TGCAGCCTTGGTTAG | 68519 |
| rs242869844 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525774 | AAGTAAGTTCCAGGA[C/T]AGCCAGGACTATACA | 68519 |
| rs242870269 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464056 | CAAAGCACACGAAAG[C/T]CATGTGATGCATGGC | 68519 |
| rs242880132 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108481462 | CGTGGCCATGTAAGC[A/G]CCAGAAAACAATATC | 68519 |
| rs242884655 | in-del | -/AAGAA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489497 | AGGAGGAAGAGGAAG[-/AAGAA]GAGGAAGAGGAGGAA | 68519 |
| rs242907594 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108441931 | GTAGCTTAGGGAAGA[A/C]TATGCAGCTACAGGG | 68519 |
| rs242912681 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108531920 | GTGTGATGAGGCGCG[A/T]GCCTCCTGTGTTCTG | 68519 |
| rs242939008 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108516004 | CTCAGAGTTAGGTCT[A/G]AGAAAGAAGGGAAAC | 68519 |
| rs242966599 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460385 | ACGAGTTCAGATAGG[A/G]GATGGATGTCCCGCC | 68519 |
| rs242973559 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447307 | AACGAGGATGAGTGG[A/G]TAGTTCTTTTAGATA | 68519 |
| rs242976494 | in-del | -/TTG | | | intron-variant | Eml1 | Mm_Celera | 12:108464985 | CTCTCCTTGCTTTTT[-/TTG]TTTGTTTGTTTTTGG | 68519 |
| rs243003543 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446872 | TGAACTGCACCCCCT[G/T]TGCAGAAGGGCTAGC | 68519 |
| rs243018570 | in-del | -/AAA | | | intron-variant | Eml1 | Mm_Celera | 12:108519377 | TTTGTAACCTTTCTT[-/AAA]AAAAAAAAAAAGTTC | 68519 |
| rs243043192 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442167 | ATTGCGTGACCAAAC[A/G]TGGGGAAATGGTAAA | 68519 |
| rs243044596 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108435736 | AAAGGAAGGGACAGA[C/T]TGTGGCTCAGGGTGC | 68519 |
| rs243062068 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108382243 | AAGGGAGATGACTCA[C/G]TAGGGATGAGTGCTT | 68519 |
| rs243075220 | snp | A/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108539060 | GTACATTTGTACCCA[A/T]CCAAGTGGGTCAAGT | 68519 |
| rs243079703 | in-del | -/GGGGGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450263 | CACTTCCGGGGGGTG[-/GGGGGT]GGGGGGTTTATCTCA | 68519 |
| rs243095225 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108490997 | GTGACTCTGAAGTGA[C/T]TGCTCCTTTCTTTGG | 68519 |
| rs243102178 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108441812 | CAAGAGAGAGAATCC[A/G]GAATCCTGAGCATGC | 68519 |
| rs243111739 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108430864 | TCTCCTAGGCCGCTG[A/G]TGGTCATCCTTCTTT | 68519 |
| rs243111945 | in-del | -/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538986 | TGTCCTCGTATAGAG[-/T]TTAACAACTTACGAT | 68519 |
| rs243136462 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108388568 | GCAGCTCCATCCTTG[A/C]CCATGATACCTGCCT | 68519 |
| rs243139762 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108416154 | GAGAGAGGGTCGTCA[G/T]CCCCCTCCCCCAAAA | 68519 |
| rs243143367 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108527254 | GGAAGTGGTTAAAGA[C/T]GGTGAGGCTGGCATC | 68519 |
| rs243152903 | in-del | -/GA | | | intron-variant | Eml1 | Mm_Celera | 12:108441322 | GAAAAGCGGGTTCTC[-/GA]GGACCACTTCCGGAT | 68519 |
| rs243153243 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108440034 | GACCTGTAGGGGACC[A/G]GCTTTCGTTGTATTG | 68519 |
| rs243154193 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108418676 | tctctctttctctct[C/T]tctctctcGTATGTG | 68519 |
| rs243154648 | snp | A/G | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108538240 | TTAGTCCCTGTGGGA[A/G]CCCGAGGACGCAGAC | 68519 |
| rs243178487 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108490494 | CTCACAGGGGCTTCC[A/G]GAGGAGCTCTTGGAT | 68519 |
| rs243180327 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108498689 | ATTCTATGTGTATGA[A/G]AATTTTGCCTGCATG | 68519 |
| rs243212796 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108497702 | GCAACCAAAGATTAT[A/T]TCTCTAGCAGCATTT | 68519 |
| rs243233279 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108384901 | CTGAGAAATACCAGC[C/T]GTGGCTCAGTCAGTG | 68519 |
| rs243247226 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108517435 | TGCACACTCATGCAC[A/G]TACTTGTGGAGGCCA | 68519 |
| rs243249492 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436077 | CTCTCCACAGGATGC[A/G]GCCCTGCTCTCCTTC | 68519 |
| rs243275168 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381656 | CTGGAAGATTTGGTT[C/T]CAGGACCAGCAAGAA | 68519 |
| rs243284080 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462618 | CACCCCCTAATCCTT[C/T]CCAAATAGTTCCACC | 68519 |
| rs243319223 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462086 | ATTGCCACCCCTTTT[C/T]GCTGTGACATGGCTC | 68519 |
| rs243319289 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108469434 | GCTGGTTCTAGATTC[A/T]GTTAAGTTCACAGTT | 68519 |
| rs243331198 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374541 | TTGCTCTATCAAGGT[C/T]AGCTCCCTTCATACT | 68519 |
| rs243365802 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108399848 | TTCTCCATCCAGTTT[C/T]CCCTCTCCAACAGTC | 68519 |
| rs243383485 | in-del | -/TTT | | | intron-variant | Eml1 | Mm_Celera | 12:108515699 | CGCACAGATCAGACC[-/TTT]TTTTTTTTTTTTCCC | 68519 |
| rs243389968 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467522 | AGAGTCGGCACACGC[A/G]CAGCCTTCCTCTGCC | 68519 |
| rs243404784 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469042 | GACAACCAAGGCTGA[A/C]AGTGCTATATCCAGC | 68519 |
| rs243415794 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108497027 | GATTCCCAAAACTCA[C/T]AAAAAGAACTGGGAC | 68519 |
| rs243427741 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108466952 | ATATCCTGAAGCTGC[A/T]GTTAACAGGCAGTTG | 68519 |
| rs243484516 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108395712 | AGGTCATTAAGAAAG[A/G]CAACCCTCCCTCCCC | 68519 |
| rs243491896 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108454698 | TTCACTATGTAGACC[C/G]AGCTGGCCTGGAACT | 68519 |
| rs243516252 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486653 | AGTCTTCACTGTCCC[C/T]TGGCTCTTTGTGTCT | 68519 |
| rs243527050 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108503971 | TGGTCACCAAGGGAT[A/G]AACGGCAACTTGGGT | 68519 |
| rs243533792 | snp | A/C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404693 | GCAAATACACACACA[A/C/T]GAACACACACATGCA | 68519 |
| rs243546139 | snp | C/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402834 | CTTACCTCTCCTCGG[C/G]TTTATGTCCCTGCCT | 68519 |
| rs243547066 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443172 | CTATGAAAGAATAAA[C/T]GTTTCTCTTTATGAT | 68519 |
| rs243556916 | in-del | -/TGCACA | | | intron-variant | Eml1 | Mm_Celera | 12:108494887 | GTGTGTGTGTGTGCG[-/TGCACA]CGCGCACGCTCACCT | 68519 |
| rs243557524 | snp | C/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108537072 | CTGCACCCAGAAGGG[C/T]CCAGTGGATGCAGGC | 68519 |
| rs243561254 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108426001 | GGGGAGTGGTGTGTG[C/T]ACGTGTGCATGCACA | 68519 |
| rs243597935 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108501135 | TACATGGTGTCCACC[A/G]TTGTATAAAACTCTG | 68519 |
| rs243609990 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108522237 | CTCAGGATCTCAGGA[C/T]CCCAGGATCCCAGAA | 68519 |
| rs243611571 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108382125 | TGTTCTGATTTTATT[G/T]AAACAAATTTCAGTG | 68519 |
| rs243632782 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433097 | CGGCACGTCTTACTG[C/T]GAGACGCGAGATCCT | 68519 |
| rs243636469 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388753 | TGTGTGTGTGTGTGT[A/T]TTGCACATGCAAGTG | 68519 |
| rs243641092 | snp | C/T | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108369962 | GCTGGCGAGATGGCT[C/T]AGCGTGTAAGAGCAC | 68519 |
| rs243668947 | in-del | -/CCTTTAAAAG | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411506 | TGAAACCTTTAAAAA[-/CCTTTAAAAG]CCCCACTGGGATAGT | 68519 |
| rs243694177 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478056 | GAGCCGGGGTTATTA[G/T]GTACAGAGGAGAAAA | 68519 |
| rs243702604 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485181 | GAGGAAAAGATGGGT[A/G]ATCGACAGGAGCCCA | 68519 |
| rs243703268 | snp | C/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369234 | GGTTGGTAGAGTTCA[C/G]GAGCAGGAGCAGTGG | 68519 |
| rs243718573 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108434824 | TACTCACACCATGTA[C/G]TACACATACATATAC | 68519 |
| rs243729794 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108529560 | CCTACAAGATAAACA[C/T]CACCGTCGTCGATCT | 68519 |
| rs243773528 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471063 | ATATCTTAAGCAGCA[A/G]AAGCATCGTTGCATT | 68519 |
| rs243779319 | in-del | -/CCACA | | | intron-variant | Eml1 | Mm_Celera | 12:108374470 | CCAATTCCAGTGCAG[-/CCACA]CCACTTGTCCCTAGA | 68519 |
| rs243797997 | in-del | -/GTGTGTGTGTGTGTGTGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433954 | AGAGAGTGTGTGCTC[-/GTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs243807879 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108470534 | ACTGGAGTTGTGGAC[A/G]GTTGTGAGCCACTGT | 68519 |
| rs243831752 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438199 | GCTGGCTGTGTATAG[C/T]CTGTGTTCACAGGTC | 68519 |
| rs243865610 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108492226 | ACAGCCCTGTTGCTT[C/T]GCAGCCTGTCCAGGA | 68519 |
| rs243871484 | in-del | -/ACACACAGACAGACAG | | | intron-variant | Eml1 | Mm_Celera | 12:108391060 | CACAGAAAGAGACAC[-/ACACACAGACAGACAG]ACAGACAGACAGACA | 68519 |
| rs243880209 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108483933 | CATTCACATGCATAC[A/C]CACAAGCAAATGTCT | 68519 |
| rs243884008 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108394025 | TTTAATCTGTGTAAA[A/T]TTCTAAGCACATTTC | 68519 |
| rs243886393 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108483957 | AATGTCTATACACAG[A/C]AAATTAAAATAAATA | 68519 |
| rs243903080 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443610 | CCACTGGCATCTCGA[C/T]GCTGCTGCCTTCAAA | 68519 |
| rs243905284 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402000 | ATAAGCCACAAGCTG[G/T]GGTTCTGTGGCGTGT | 68519 |
| rs243915750 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108419183 | GGGATTGGCTTAGTC[A/C]CTCAGCATAATGTTC | 68519 |
| rs243919333 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108491692 | CAGCATTTAATCTCT[C/T]TACTGACAATGCTTC | 68519 |
| rs243963128 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108450271 | GGGGGGTGGGGGGGT[G/T]TATCTCAGGATATTT | 68519 |
| rs243976367 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108428711 | AGTATGTCTCCTGCC[C/T]TTCCAAGGTGGCCAG | 68519 |
| rs243979386 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418138 | CTGTGATTCTAGAGA[C/T]TAGAAGGCTGCCTCC | 68519 |
| rs243984189 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412817 | AGAGAGAGAGAGAGA[-/G]AGAGAGAGAGAGAGA | 68519 |
| rs243986715 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526223 | TTGAGCTGTTGGCAC[C/T]CCGGCTGTGAATGCA | 68519 |
| rs244008782 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108391961 | TAGGTATGCCTACTA[A/G]ACCAGAGTCTGAGTG | 68519 |
| rs244020242 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108525763 | CCTGTCTAACAAAGT[A/G]AGTTCCAGGATAGCC | 68519 |
| rs244029030 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524601 | GTACACTAGCCGCTT[C/G]ACAGCATACCTGAAC | 68519 |
| rs244032556 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108428061 | ATGGAGCCCAGGCTG[A/C]ATAAGAACACTGAAC | 68519 |
| rs244066966 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108391104 | CAGACAGACACACAC[A/C]CCAATGTTCCCAAGG | 68519 |
| rs244106385 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524262 | GAAAAACAAACAAAC[A/G]AAAAGACCGTATAAT | 68519 |
| rs244114162 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108529823 | AGTTCCACGAAGCTG[C/T]CCTGGGTGGGTAGTT | 68519 |
| rs244128281 | in-del | -/A | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445049 | TTTGCAAAGAGATTC[-/A]ACAGTGGCAAGATTT | 68519 |
| rs244133004 | snp | C/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536925 | CTGGTGTGTACTCAG[C/G]CCTCTAATATACAAT | 68519 |
| rs244141787 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108530512 | GCTCACTAGACAGCG[A/G]ACCTTTTCGTCACTG | 68519 |
| rs244194869 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108495991 | GAGCGGGGCCTGAGG[G/T]AAGACTGCAGTGTTG | 68519 |
| rs244205553 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108485102 | TCTTGGCACAAGGTT[C/T]TAGCTGAAGGACTTG | 68519 |
| rs244226507 | in-del | -/GG | | | intron-variant, frameshift-variant | Eml1, Gm33385 | Mm_Celera | 12:108411054 | TCTGGCGTGGCTCCA[-/GG]GGGGGGCAGGATAGG | 68519 |
| rs244243775 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403104 | CAGTACATTTAAGGC[A/C]GTTCCCACCACTGAT | 68519 |
| rs244244439 | in-del | -/AC | | | intron-variant | Eml1 | Mm_Celera | 12:108440115 | ACTGTGCCTCACCCA[-/AC]ACAGTCTAAAGAGTC | 68519 |
| rs244249356 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108493110 | ATGTGTCTCTCTTCT[C/T]AGGGACTGCCCAAGT | 68519 |
| rs244259958 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108501716 | ATTAAGTTCCTTAAA[-/T]TGGAAGAGGAAAAGT | 68519 |
| rs244273973 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451838 | GGATAGGGAAATAAT[A/G]GTAGATGTGATACTG | 68519 |
| rs244278974 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108520364 | acacagacacacaca[C/G]acacacacacacaca | 68519 |
| rs244279881 | snp | C/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403744 | GGTGTTTTGTTTTGG[C/G]GGAGGGTTTATCAGC | 68519 |
| rs244285851 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108475086 | GCTCTGCTCAGCCGC[-/T]TTTTTCTATCCTTCA | 68519 |
| rs244289708 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422270 | ACCGAAAACTTCAGA[A/G]TTTTACCTCTAGTGG | 68519 |
| rs244315363 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108501578 | TTAATGGTCATATGG[A/C]TGGTTCCAGCCCTTC | 68519 |
| rs244362301 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442846 | GTGTATGATATGTTT[A/G]TGTGAAGTGGCTCCT | 68519 |
| rs244366349 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449202 | ATTTAAGATCTTGCC[A/G]TCTCCACCTTCTCAG | 68519 |
| rs244396096 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527786 | ATCCACCCTACCTGC[C/T]GCTGCCCCGCAACAG | 68519 |
| rs244403525 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448735 | AAACAGATTTGTTTA[C/T]GGAACGAAAACATGC | 68519 |
| rs244417917 | snp | A/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408913 | GGAGCCTCCCAGGCC[A/T]GGACTGAGAGCAGTG | 68519 |
| rs244440648 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108456963 | CTCACTAGCCCAGTC[C/T]AAAAAGCCCCTAACT | 68519 |
| rs244478531 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527000 | GCCCCTTGCCAGACA[A/G]CTAACTGCTTTGACC | 68519 |
| rs244478545 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108533481 | CCTCTCTCCCTTCCG[G/T]CTCTCAGACTGTTTA | 68519 |
| rs244488671 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108508056 | GGCATTTTGGCAGGG[-/TT]TTTTTTTTTTTCACT | 68519 |
| rs244493367 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108416442 | CTCCCCAGAAGTCTG[A/C]GCAGGGCTCTCCCTT | 68519 |
| rs244506964 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108533165 | TTCTTTCCTGGTACC[A/G]ATGCTTGAAGCTATA | 68519 |
| rs244523712 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508012 | GTGTTTTAAAAGACT[C/T]GAAACAAGAAAATTT | 68519 |
| rs244540660 | in-del | -/CAC | | | intron-variant | Eml1 | Mm_Celera | 12:108529361 | CCACATCAGGCAGCT[-/CAC]CACCATCCATAACTC | 68519 |
| rs244551655 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421688 | GTTGTTTGATAACAA[A/G]TGCTGACTCTGGCTG | 68519 |
| rs244583236 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108514287 | GTGAAGTCGGTGGGG[C/T]TTGAGAGACTCAGTG | 68519 |
| rs244616988 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108518992 | ATTGTTTTTTTCTGT[A/T]TGTGCTTTCTTTTCC | 68519 |
| rs244619524 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108477838 | CTCTGGGGACAGAGC[A/G]GACCGGGGCTCTGAG | 68519 |
| rs244621743 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482378 | CATGAGCAGTGCACA[A/C]ACCTGCCCTGATGCA | 68519 |
| rs244665385 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532886 | CTTGTGGCTTTTCCA[A/G]GGCTACTTGCAAGTA | 68519 |
| rs244674539 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489715 | CATGCATACAGGCAA[A/G]ACATCCATACACATA | 68519 |
| rs244690799 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108451979 | ACCTAGTAAAGATTC[C/T]ACACACTCCCAAATA | 68519 |
| rs244691167 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445558 | GTGCTTTGCAATTAC[C/T]AGCCCTGTGGATTCT | 68519 |
| rs244702379 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108497093 | GAGGGCAGAGACTAA[C/G]AGATCCCTGAAGCTC | 68519 |
| rs244709943 | snp | A/T | | | downstream-variant-500B, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108539791 | AGTAACCCAATCCAA[A/T]TGTTAGTTTCTTTGT | 68519 |
| rs244763617 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108507524 | ACCAACCACTTGTTT[-/C]TTTTGAAACAGGGTC | 68519 |
| rs244794198 | in-del | -/TC | | | intron-variant | Eml1 | Mm_Celera | 12:108448171 | GTGTCTGTCTGTCTG[-/TC]TCTGTCTCTGTCTGG | 68519 |
| rs244809859 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108426854 | TAATTTTGCATATGT[A/G]CATTTCTGTGGAGGG | 68519 |
| rs244812472 | in-del | -/GGCCT | | | intron-variant | Eml1 | Mm_Celera | 12:108436406 | TAGGAGCCTTTGCCC[-/GGCCT]ACACAAGTCTGCAGT | 68519 |
| rs244816457 | in-del | -/CACACACACA | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409797 | TCTCTCTCTCTCTCT[-/CACACACACA]CACACACACACACTG | 68519 |
| rs244838110 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405065 | ATGACTCTGCAAGTC[C/T]AGTCTGCCCAAGGCC | 68519 |
| rs244870293 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429934 | TGAGGACACAGAAAA[C/T]GGCTCCAAGCCTCGC | 68519 |
| rs244870354 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108394450 | CTATGGCCTGGAGCA[C/T]GTGTGGAGATCAGAG | 68519 |
| rs244887346 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108426395 | TGAGAGAACAGGCTC[A/T]CTCCTTCCACCATGT | 68519 |
| rs244888129 | in-del | -/GATCTGGAGA | | | intron-variant | Eml1 | Mm_Celera | 12:108503449 | TAGGAGGTCTAAAAG[-/GATCTGGAGA]GATCTGGAGAGATCC | 68519 |
| rs244896655 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108429640 | TAATTGCCGCACGGG[-/C]CCTCCACCCAGCGAG | 68519 |
| rs244902116 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455548 | CCTGGCTATAGAGGT[A/G]GCCACCTCCTTTGTG | 68519 |
| rs244915379 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108476998 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTA | 68519 |
| rs244921704 | snp | G/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413486 | ATGGCAATGTCTCTC[G/T]GTAAATGGAGGAAGT | 68519 |
| rs244923888 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108469213 | TCGCACCCACCAAGT[-/G]GGGTGGGGTCAGGTG | 68519 |
| rs244943117 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460359 | CAAAAATAGAAGCAT[C/T]CCTGGTCCGAACGAG | 68519 |
| rs244957796 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108425131 | AGGCTTTCATGAAGT[A/G]AAAATATAAATGAAT | 68519 |
| rs244979317 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108522022 | GCACCCAGGAACTCC[A/G]CCTGACCAGTGGCAC | 68519 |
| rs244982106 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108510434 | ACCCTGAGCTTCCTC[A/G]TAACTTCAGCCAGTT | 68519 |
| rs245008994 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432830 | AGAGCTCGAGACACT[C/G]GAGTGCCCTTTCTCA | 68519 |
| rs245021234 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108480254 | TGTGTGTGCATTTAA[A/G]CATGCTCTCTCTTGC | 68519 |
| rs245039326 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108466289 | TGATGGTCAGATCAG[C/T]CCTGTGTGCCCCAAG | 68519 |
| rs245040687 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502566 | TCAGATAACAGCAGG[A/G]TCACCAGGAGACAGG | 68519 |
| rs245063484 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518026 | GATCCCATCTCAAAA[C/T]AAATAAATAAATAAA | 68519 |
| rs245066429 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372211 | GTCCTTAGTTAAGAC[A/G]TGGCTCAGCTCTGGC | 68519 |
| rs245108297 | in-del | -/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406702 | GCTCCACTCTTGGTG[-/C]CTGTGACAGCCTACT | 68519 |
| rs245112698 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108388728 | GTTTGATATATATAT[-/G]GTGTGTGTGTGTGTG | 68519 |
| rs245113834 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448099 | TGGGAGGGGTGTGGG[-/T]TTTTTTTTTAAGGTT | 68519 |
| rs245121713 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108371705 | TGACACCATATGCAA[C/T]GGAAGGGGTGTAAGC | 68519 |
| rs245122913 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465159 | GCTGGGATTAAAGGC[A/G]TGCGCCACCACTGCT | 68519 |
| rs245142184 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453110 | GTGTATGTATGTGTG[A/T]ATATATGTATGTGTG | 68519 |
| rs245146296 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407002 | CTTATACCCATACTT[C/T]GTTTTTATGGCCGAG | 68519 |
| rs245154845 | in-del | -/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108481326 | ACATCATTCCCACAG[-/T]TGCTCTGTGCCAGTC | 68519 |
| rs245170781 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472719 | CGTGAGCTCTAGGTT[C/T]ACCTGAGAGACCCTG | 68519 |
| rs245172165 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455489 | ACCATTAAGGAGACT[A/C]TGGTGGCAGTGGAGG | 68519 |
| rs245214023 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504856 | TGGGTCCTAGAGAGA[G/T]GGTGCAGCAATAAGA | 68519 |
| rs245219199 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108452201 | GCTAACATAGTTCTT[C/T]GTTTTGTCCATGAGT | 68519 |
| rs245249767 | in-del | -/ACACACAC | | | intron-variant | Eml1 | Mm_Celera | 12:108390048 | CCTTAAAAAAAAAAA[-/ACACACAC]ACACATTGTAGGAAC | 68519 |
| rs245273424 | in-del | -/GA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457457 | TATGTGTGAGTGTGT[-/GA]GTGTGTGTGTGTGTG | 68519 |
| rs245278700 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108461943 | TGAGGTATCTGGTGA[G/T]GAGCAGAGCTGGAAT | 68519 |
| rs245303384 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108406068 | GCTTTCTCTTTCTCC[C/T]CTTCTCCCTTTTTGT | 68519 |
| rs245317008 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108461871 | ACAGAACCCATCGAC[C/T]GTCACAATAACAGCC | 68519 |
| rs245323344 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108512556 | AATAATCAGGGATAG[A/C]GAGATGGTTAAGAAT | 68519 |
| rs245329012 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390854 | agacatacagacaca[C/T]acactacatacatac | 68519 |
| rs245339975 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108394050 | CATTTCTAAAGGGTG[C/T]CTGCTTTATTGGCCT | 68519 |
| rs245342341 | in-del | -/CTT | | | intron-variant | Eml1 | Mm_Celera | 12:108420480 | TTCCTTCCTTCCTTC[-/CTT]CCCTCCCTCCCTCCT | 68519 |
| rs245347495 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108462775 | CAAGGAAGGTGTCCA[-/G]GGGCTGGGAACTGTG | 68519 |
| rs245352445 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429054 | TTTCCATTTATTTCT[C/T]CTGTAAGAATTAACA | 68519 |
| rs245355391 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108512430 | GTGCACACCACCACA[A/G]CCCAGCTGCGGGTCC | 68519 |
| rs245368942 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108397047 | CCCGCCCAGGAATCT[-/AG]AGAGAGAGACAGGGC | 68519 |
| rs245377280 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504373 | CAGGGGCCGTGGCTG[A/G]ACCAGTGTGCATGGG | 68519 |
| rs245410474 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503849 | CTGGGTTGATCCCTG[C/T]ATTACAGAGTTAGCA | 68519 |
| rs245411656 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108505527 | TGCATCTCTGCGTGC[A/G]CTTCTGCTGACTTCA | 68519 |
| rs245424508 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380272 | CCCTTCCATAACCCC[A/G]AGGATACCGGGATCT | 68519 |
| rs245426471 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108375333 | GCAAGATAATCTTTT[A/T]AAAACTACATTTCTG | 68519 |
| rs245445466 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468364 | CCAGGCCAGCCTGGT[C/G]TACAAAATGAGTACA | 68519 |
| rs245448408 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108373912 | GCACAGCTTTTTCAA[A/C]GCTTGTGTTTCAGAC | 68519 |
| rs245455587 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108427212 | GTTAACACTGGGTTT[-/A]ATATTTTAATGAGCC | 68519 |
| rs245477993 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519479 | TTGGTGCCATCCCTC[A/G]GGAGCGGTCCACTTC | 68519 |
| rs245483119 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380755 | AAAAAAAATCCTTGC[C/G]CAGAATGATGATTAC | 68519 |
| rs245488639 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108510653 | ATACATGATCAACAC[G/T]AAAATATACCAATCT | 68519 |
| rs245492519 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108385894 | CACTCACACCTCCCC[C/G]TACCCCCAGCCTCTG | 68519 |
| rs245508488 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379684 | TATTATTTATTTTTT[G/T]TTTTTGTGACAGGGT | 68519 |
| rs245511738 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437037 | TTCTCTGGAACTGAC[A/G]ACAGATAACTTTTCC | 68519 |
| rs245541853 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108476393 | GTCTATTTCAAGAAA[C/G]CATTGTGGGATCCCA | 68519 |
| rs245543027 | in-del | -/TCTGGGAGGATCGC | | | intron-variant | Eml1 | Mm_Celera | 12:108467609 | ATGCTTTTGTGTGAT[-/TCTGGGAGGATCGC]TCTGTGTAGCACTGT | 68519 |
| rs245548862 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474335 | ACAGAGAAACCCTGT[A/C]TCAAAAAACAAAAAC | 68519 |
| rs245575082 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108483027 | GATAAGAAAGCTTTA[A/C]TTCTAGCTTTTTGGG | 68519 |
| rs245583429 | in-del | -/TTTC | | | intron-variant | Eml1 | Mm_Celera | 12:108476978 | GCTTTTTTTTTTTTT[-/TTTC]TTTTCTTTCTTTCTT | 68519 |
| rs245592683 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108493185 | GTTCCAGGTTAGGGT[C/T]TGTCACTCCAGGAAA | 68519 |
| rs245619837 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473852 | AGTGCAAGCAACTTA[A/G]GAATAAAGGTTAATT | 68519 |
| rs245646615 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482489 | ATTGTTTTCTTTTTA[A/G]CGGATTTATTTATTA | 68519 |
| rs245657661 | in-del | -/AC | | | intron-variant | Eml1 | Mm_Celera | 12:108499011 | ATAAATCTTAAAAAA[-/AC]AAAAAAGAAGAGATG | 68519 |
| rs245665366 | snp | G/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108410120 | GAGGACAACTTGTGG[G/T]AGTCAGTTCTCTTAC | 68519 |
| rs245668079 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108464702 | GAGATAGCTCAGTCA[A/G]TAAAGTACTTGCCAT | 68519 |
| rs245677614 | in-del | -/ATT | | | intron-variant | Eml1 | Mm_Celera | 12:108378663 | GTAGTAGTAGTAGTA[-/ATT]ATTTCCCTGTTGTTT | 68519 |
| rs245677733 | in-del | -/TA | | | intron-variant | Eml1 | Mm_Celera | 12:108448152 | GTGTGTGTGTGTGTG[-/TA]TGTGTGTCTGTCTGT | 68519 |
| rs245678679 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108516679 | CCGTTTGGATTCGCT[C/G]GGGGGGGGGGGGGGG | 68519 |
| rs245690903 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108507345 | CCTTTAATCCCAGCA[C/T]TTGGGAGGCAGAGGC | 68519 |
| rs245717766 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409385 | ATTCTGAGCTGCTAC[A/G]GAATGGTCTTAGGCT | 68519 |
| rs245733616 | in-del | -/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376343 | CTTCTCCTCCCCGCC[-/T]TTTTTTTTTTTAAGA | 68519 |
| rs245741251 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392638 | GAGCCTTCTCCAAGC[C/T]ATGCAAATGAAGCCC | 68519 |
| rs245770882 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442501 | ATGTGCTTGCAGCTC[G/T]TTACACTGGAACATT | 68519 |
| rs245798021 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432340 | TAGATAGAGATTTCT[C/G]TATTTTGCTCATACA | 68519 |
| rs245803343 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383205 | CTTTATTGCTTTCAG[C/T]CTTTTTATAGCTTTT | 68519 |
| rs245806059 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108514343 | ATCCTAAGAGGCCTG[C/T]GGCATTTGATGCTCT | 68519 |
| rs245806114 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108506251 | CAGATTCTGAACCTT[A/G]TGGGATGGAAGCCAA | 68519 |
| rs245812391 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381026 | GAGGGGCGGGGAGCA[-/G]GTAACAGGGAGAGAG | 68519 |
| rs245814992 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108529329 | TTTGTCCCCTCCCGT[C/G]CCCCCCTCCCCCCAA | 68519 |
| rs245834107 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108489563 | AGATGACTCATCAGT[C/T]AGGACCACTGGCTGT | 68519 |
| rs245840818 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433660 | TAGTGAAACGCACTC[A/G]GCTGCCGCTCCCCAG | 68519 |
| rs245849604 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108528684 | GAGCAGCCCTCAAGG[A/G]ATGTGGGCCGAGACC | 68519 |
| rs245857130 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108448310 | CTCAGGACCTCTTCT[A/G]CAAGATCAGGAAATG | 68519 |
| rs245874555 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108389258 | ACAGAGGCAGGAGAA[C/T]TTGCTTGAGCCCAGG | 68519 |
| rs245885503 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108394283 | GGTCATATTCTGGGC[C/T]GGAGAGTCTGTGTGC | 68519 |
| rs245886139 | in-del | -/GC | | | intron-variant | Eml1 | Mm_Celera | 12:108429150 | TGTGCGCGCGCGCAT[-/GC]GCGTGCGCGCATATG | 68519 |
| rs245906724 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440649 | CTCCAAAGATCTTAT[C/T]CATTTCTGAGTAGCA | 68519 |
| rs245915466 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108381171 | GAGAGGGGCGGGGCA[C/T]AGGGAGCTGGGAGAG | 68519 |
| rs245942863 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108401592 | TACCTTGGGCCCAAG[A/C]TTAGGTATGCCTCCT | 68519 |
| rs245952823 | in-del | -/TGC | | | intron-variant | Eml1 | Mm_Celera | 12:108420518 | CCTATCTTTTATTGT[-/TGC]TGTTGTTTTGTTTAT | 68519 |
| rs245957615 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486031 | ATGTGTCCAGCCAGC[C/T]GGCCCCTCTTCCCCT | 68519 |
| rs245963339 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369631 | AAGGCCTCAGTGCCC[A/G]TGCAAGACTTTCCAG | 68519 |
| rs245965073 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108386312 | TGGCTAAGGCTGCTA[C/T]GCATTTTCTCAAATA | 68519 |
| rs245978398 | snp | C/T | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108536219 | CACAAGGCTGTTGCT[C/T]CCTCCAGGGGTTCCG | 68519 |
| rs245979343 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108387397 | TCTGCAGATGATGGC[A/G]CCACTTTGGGAAGTT | 68519 |
| rs246003845 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108417272 | ATGGGAAAGGAAGAC[A/G]GGCACTAAGGACAGG | 68519 |
| rs246004566 | snp | A/G | | | intron-variant, synonymous-codon | Eml1, Gm33385 | Mm_Celera | 12:108401155 | CCCATGGGAGGGGGC[A/G]GTTAGAGCCAAGGGA | 68519 |
| rs246012303 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518213 | AGAGAGAATCCTACA[C/T]CCTCTATGGACTTCC | 68519 |
| rs246019092 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108499882 | AAGGTGGATCCTGTG[C/G]TTACAAGGGCTGTAG | 68519 |
| rs246041344 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108377336 | TATCCTGCGTTCTGG[C/T]GTAGGCCTCTTTCTC | 68519 |
| rs246048816 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108463391 | GTCCACAAAGTGAAC[A/C]GTCTCACGTGATTCT | 68519 |
| rs246054526 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108498969 | TGTGTCTGAAGACAG[C/T]TACAGTGTACTTAGA | 68519 |
| rs246058794 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108506126 | TGTCTGTTGGGTTTC[A/G]TTTCCTCTGGAAAAC | 68519 |
| rs246078664 | in-del | -/CTGGGGG | | | intron-variant | Eml1 | Mm_Celera | 12:108465872 | TGCGCATCTGAGGCT[-/CTGGGGG]CTGGGCCTGAATTTT | 68519 |
| rs246083010 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108426146 | GGCTGGCTGTTTTGG[C/T]TAGAATAGCTGGCCA | 68519 |
| rs246103873 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470995 | TCTTCTGCTATGCTA[C/T]GGTTGGTCTGAGGAT | 68519 |
| rs246121908 | snp | A/G | 0.5 | 0 | intron-variant | Eml1 | GRCm38.p3 | 12:108384632 | TCAGCACATTTAAAC[A/G]GACAGACAAACAGGA | 68519 |
| rs246129490 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108467999 | TGGTCCAGGTAGTCC[-/A]AAAAAAAAATGGCTG | 68519 |
| rs246133895 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108521978 | CATCTGCCCCAACAC[C/T]AGAAGTAACAGGGAC | 68519 |
| rs246169311 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480532 | AGCAGTTCATCTAAT[A/T]CACCTGCTCCACCCT | 68519 |
| rs246176148 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433380 | CTCTTGGCAAAGTCA[A/G]AATTTTTAGCAGTAA | 68519 |
| rs246197912 | in-del | -/GAGAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108438931 | AGGAAAGGAGGGAAG[-/GAGAAA]GAGAAAAGATGGCAC | 68519 |
| rs246202507 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108398802 | AAAGACTCTGACTCA[C/T]GTGGGACAGAGAGGA | 68519 |
| rs246208665 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108489471 | GGAGGAGGAGGAGGA[A/G]GAGGAGGAAGAGGAG | 68519 |
| rs246212360 | snp | C/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538359 | GTTGGGGAGCCAGTG[C/T]GTGTCACACCAGATA | 68519 |
| rs246212418 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108531044 | GCATGTGTGGTTTAT[A/G]TATGTATGTGTGGTT | 68519 |
| rs246226127 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108420482 | CTTCCTTCCTTCCTT[-/C]CCCTCCCTCCCTCCT | 68519 |
| rs246232945 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108440160 | GGCTTTCCTAGAGTA[A/G]GTCCTCTGGAGGTAG | 68519 |
| rs246248426 | snp | A/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536511 | CACTAGAGTTACCCA[A/T]AGTTGTGAGCTGCCA | 68519 |
| rs246266801 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108401982 | GTTGTCCTTAGCATA[A/G]TTATAAGCCACAAGC | 68519 |
| rs246275026 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108487673 | GCAGATTCTGATATG[A/G]TCCTAAACATATTTT | 68519 |
| rs246284919 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479003 | CTTTATCATGAAAGG[-/T]TTTTTTTAAAAAAAA | 68519 |
| rs246303943 | snp | C/T | | | synonymous-codon, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538111 | TTTCCAGGCTCCAAG[C/T]CACATCTACAGTGGA | 68519 |
| rs246304154 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108517549 | CACCTACATCTGTGC[-/G]GGGGGCCATAAGTGT | 68519 |
| rs246316921 | in-del | -/GTGTGTGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517369 | GTGGTATGTGTACAC[-/GTGTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs246346825 | in-del | -/GCCC | | | intron-variant | Eml1 | Mm_Celera | 12:108431403 | CAGTCTGTATCTATA[-/GCCC]ACCCCAGCACTGGGG | 68519 |
| rs246353531 | snp | A/C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502531 | GGTACTCAGACAACA[A/C/G]ACAGTCAGTCATTGG | 68519 |
| rs246357354 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108475213 | ACCAACAAAACTGAC[-/T]TTTTTTCTGTAAATT | 68519 |
| rs246371336 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403442 | CCTCTTGGTTCATTT[A/G]TGTTGTAGCAAGTGT | 68519 |
| rs246396560 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403747 | GTTTTGTTTTGGGGG[A/G]GGGTTTATCAGCCAC | 68519 |
| rs246415703 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108385649 | TTGGTAGAATGCTCA[A/G]GTAGCAGAAATGCCT | 68519 |
| rs246421163 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108394736 | ATACTCACACACCCA[G/T]CTTAGCTGCAGGATT | 68519 |
| rs246486355 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437137 | GTTGAGATGGCGAAC[C/T]GGCTTATTTTTCCTG | 68519 |
| rs246496963 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469335 | CTCAGGGTCCCAGCC[A/C]GGGGATGGTTCCACC | 68519 |
| rs246500950 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390347 | ACACAAGAACATATA[G/T]ACCTTACACAAAAAT | 68519 |
| rs246506438 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520420 | GGCAACATGTGCACA[A/G]CCCTGCTCGAGGACC | 68519 |
| rs246510259 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108472659 | GCCAGTGTCTGGAAA[A/G]CAAAGACAAGAGCTA | 68519 |
| rs246518675 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438820 | TAAACCCCATGAGGC[C/T]CGTGGGCCCTGTAAT | 68519 |
| rs246525659 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484461 | TTCCCGCTGGCTCTT[A/C]CCATCATCCACATAA | 68519 |
| rs246534751 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108436442 | TCACCTCTGGATTCT[G/T]AGTGCTAAATGAGCT | 68519 |
| rs246537166 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108524500 | AAATGAAGACACATC[A/C]TAGCAAAACTTATGG | 68519 |
| rs246544877 | in-del | -/GT | | | intron-variant | Eml1 | Mm_Celera | 12:108449097 | GCATACATTGGTTTC[-/GT]TTTTTTGTTGTTGTT | 68519 |
| rs246548382 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447977 | TGGCCCAAGTTTGAA[G/T]CTGTGTGGTTTGTCT | 68519 |
| rs246548478 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455042 | GCAGATCTTCAAGCC[A/G]GAGCATCCACCGTGT | 68519 |
| rs246592563 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442343 | TGCCGTGTGCATGGC[C/G]TCCCCGCCACTCAGC | 68519 |
| rs246634413 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108371988 | TTGAGCAACTGGTTT[-/A]ATGTCTCTGAGCTTC | 68519 |
| rs246639117 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108454327 | ATGAGAATACAGATC[A/C]ACATCTGTGTTCCCT | 68519 |
| rs246651824 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442000 | GCCTCACCTGTGGAC[A/G]CTGGCTTGATACTTG | 68519 |
| rs246663343 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471607 | TGCTTGCTTCTATAG[A/G]GATGTTCACCTTTGT | 68519 |
| rs246684900 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405223 | TTGGATGTAAGGTCC[G/T]TTCTTGTATTAGCGG | 68519 |
| rs246697458 | in-del | -/CACACT | | | intron-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108537742 | ACACACACACACACA[-/CACACT]CTCTGCCTACCTACT | 68519 |
| rs246715316 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108393443 | GAGGCAGAATAAGGC[A/T]CCAAGCCCCTCACCT | 68519 |
| rs246718288 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474211 | CACCATCAGCCAGGC[A/G]TGGTGGTGCACGCCT | 68519 |
| rs246732604 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484045 | AGTCTGAACATGTCA[G/T]CGCCAAGATGAGAGA | 68519 |
| rs246786726 | in-del | -/GGTTT | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108411935 | GGGGAGGGGGAGTTG[-/GGTTT]TTTTTTTTTTTTTTC | 68519 |
| rs246787329 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407988 | TCCTGATTCTGCTGG[A/C]TGGAAAGCCAGCAGG | 68519 |
| rs246808578 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108483363 | TTGTTTTCCCTTGCT[G/T]TCCAGAGGGACTGTA | 68519 |
| rs246811352 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108492012 | TCTGGCCTCCGATAG[A/G]GATGTATCAACCTTA | 68519 |
| rs246840671 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108491160 | TAGCAGTACACTGAT[A/C/T]GACCGCAGGAGGCGC | 68519 |
| rs246854959 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108501755 | CACATTAGCCAGGGC[C/T]ACTTGACTAGCCAGG | 68519 |
| rs246864340 | in-del | -/CATGCTCTGGCCT | | | intron-variant | Eml1 | Mm_Celera | 12:108455576 | GTGGACAGCGTCAAC[-/CATGCTCTGGCCT]CATGGAAGCAATAGC | 68519 |
| rs246896482 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108435850 | CTGTCGCCTCTGTAG[C/T]TGTGTGTGGAAGCTT | 68519 |
| rs246908341 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108493690 | TGAAAAGAGAAGAAC[A/G]AGGTGCTTGGACAAT | 68519 |
| rs246933162 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455516 | GAGGAGTTGCTCTTC[C/T]GATGTTTGTGCCAGT | 68519 |
| rs246937435 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108458069 | CTGACCCACAGCCTC[G/T]GCTTGCAAGAGCTCA | 68519 |
| rs246946098 | in-del | -/AAAAAC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474507 | CTGAATTTAGAAGAA[-/AAAAAC]AAAAACAAAAACAAA | 68519 |
| rs246956215 | in-del | -/TGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108418687 | TCTCTCTCTCTCGTA[-/TGTG]TGTGTGTGTGTACAC | 68519 |
| rs246961881 | in-del | -/AA | | | intron-variant | Eml1 | Mm_Celera | 12:108415579 | ATAAAAATAAATCTT[-/AA]AAAAAAAAAAGAAAA | 68519 |
| rs247020762 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455126 | TTTCACATCTTTGGG[C/T]TCCACCCTAGACTGC | 68519 |
| rs247022751 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108461965 | AGCTGGAATTTTAAC[A/G]CCAATGGTTTGACTC | 68519 |
| rs247056036 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393392 | GAAGGAACAGACTCT[A/G]GAGTGCCACTGACCT | 68519 |
| rs247064785 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456546 | CACAGTCTTTGTGGT[A/G]CACATCTGGCAAACC | 68519 |
| rs247070802 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108417320 | TCCAGAGTGCTCAAG[-/C]GTATGGCGTGACTGA | 68519 |
| rs247079480 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409731 | TTTCTCTCTTACATA[C/T]ACACAAACATACTCT | 68519 |
| rs247085135 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108414403 | ACTCGCGcacacaca[C/T]acacacacacacaca | 68519 |
| rs247113503 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108389545 | TGACTGTAGGCTCTG[C/T]AACACTTCCCTGATT | 68519 |
| rs247133336 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457821 | TCAGCCTTGTGCCCT[C/G]AGGCATGGTGGGAAC | 68519 |
| rs247153130 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108417106 | GATGGTCTATTTCAC[A/G]TAACACTGTGTCGTG | 68519 |
| rs247158692 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108432769 | CAGGATGGGAGCTGG[C/T]ACTTTGCCAGCCATC | 68519 |
| rs247174610 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486323 | TTACCACCGGGCCAT[A/G]GTCTGTTGACTAACA | 68519 |
| rs247174725 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108381082 | GCTCAGGGAGTGGGG[-/C]CGGGCTCGGGGCGGG | 68519 |
| rs247178010 | in-del | -/ACGCGGGCGTGG | | | intron-variant | Eml1 | Mm_Celera | 12:108429134 | GGTGTGTGTGTGTGT[-/ACGCGGGCGTGG]GTGTGCGCGCGCGCA | 68519 |
| rs247183920 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448965 | GCAGACATGCACCAC[C/T]ACATATGGTTTCTGT | 68519 |
| rs247204635 | in-del | -/GT | | | intron-variant | Eml1 | Mm_Celera | 12:108425850 | GTGTGTGTGTCTGTG[-/GT]GTGTGGGGCAGTGCT | 68519 |
| rs247230359 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108465614 | AGGGTTCACTCAGGG[-/T]TTTTTATTTTACTTG | 68519 |
| rs247237396 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108498453 | CCCAAGATGTCTGTG[C/T]TCAGCAGTGACATTC | 68519 |
| rs247242179 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108515088 | TTCGGTAAATAACAT[G/T]CCCACACTTACTCAT | 68519 |
| rs247257804 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108431447 | GGAGGGCCTTGCTAA[A/C]CACCAGTCTAAGTAA | 68519 |
| rs247261110 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438363 | TGAGAGATGAGACAG[C/T]GGATACAGAACTCTG | 68519 |
| rs247263022 | in-del | -/GG | | | intron-variant | Eml1 | Mm_Celera | 12:108397231 | CCATTCTATTGGGTT[-/GG]GGGGGTGGAGGGGGC | 68519 |
| rs247278309 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108389712 | CAAAGTCAGGCCCTT[-/G]AAGTAGGAAGAAGCT | 68519 |
| rs247278492 | in-del | -/CTCTGCAAACTGAGCCACATC | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402586 | CCTAGGAGGCGAGCA[-/CTCTGCAAACTGAGCCACATC]CTCGGCTGTTATTAG | 68519 |
| rs247282648 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108508196 | CCTGCGTTCAGTTTC[C/T]AGGATCCACTTGATG | 68519 |
| rs247310358 | snp | C/T | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108370934 | CTCCTTCACTAAATG[C/T]CCATAAATGGTCCTG | 68519 |
| rs247355167 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504745 | GGTTGGGTTAGGGGG[C/T]GTGGGGGGAAACAGA | 68519 |
| rs247356723 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383686 | AGAGCAGCTAATGTT[C/T]CTAACCACTAAGCCA | 68519 |
| rs247366786 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488749 | ATTTTCAGATGTGGT[A/G]CCACCTATTTCCAAT | 68519 |
| rs247371107 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370124 | ATAAATCTTTGGGCC[A/G]GAGCAAGCAGGGACT | 68519 |
| rs247380908 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464165 | TTGCTCGGTTTCTTT[C/T]AGTGTATGTCTTTGG | 68519 |
| rs247380941 | in-del | -/AAATAC | | | intron-variant | Eml1 | Mm_Celera | 12:108390489 | AATAAAAAAATTAAA[-/AAATAC]ACATTTTCAAACAGT | 68519 |
| rs247404915 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108515626 | CAGATGCGCACAGGG[A/C]AGCTCAGAGGCTGAC | 68519 |
| rs247408121 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492684 | AATCCTGCCTCAGTG[-/T]TCCAAGTGCTGAGAC | 68519 |
| rs247417345 | snp | C/T | | | synonymous-codon | Eml1 | Mm_Celera | 12:108463573 | GGTGTCAGACCGCAT[C/T]GCCTCTCTGGAGCAG | 68519 |
| rs247425943 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108382410 | GGTGAACTTCCGGTT[G/T]TATGAGTGACCCAAG | 68519 |
| rs247432003 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447740 | AACCTTGCCCGCTTA[C/T]ATGAGGGAATGACCA | 68519 |
| rs247432249 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478940 | GGTTTCCTGTGTGCC[G/T]TCTGCTCCACGGGGA | 68519 |
| rs247458867 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108374450 | TTCCTTCCATGTAGC[A/G]TCTGCCAATTCCAGT | 68519 |
| rs247460815 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496385 | ACTCCACACAGGCTC[A/G]GAGTGGCCTGGACAT | 68519 |
| rs247469072 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478297 | CCTACATAGTGTGTG[G/T]GGTTTTAAATGTTCT | 68519 |
| rs247471100 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486158 | TCATTAGGTATCCAT[G/T]TGTATCCATTATATA | 68519 |
| rs247485215 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404820 | CACGTGCAAGTGCAA[A/G]TACACACACATGCAC | 68519 |
| rs247508368 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402084 | CTGGCCAGCATTAAA[C/T]TCATGGAGATCCTTC | 68519 |
| rs247544343 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108450487 | ATCTTATGACTGTGA[G/T]AAGCATGGGAGAGTC | 68519 |
| rs247560203 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108485202 | CAGGAGCCCAGCGGG[A/G]ACTGCGTGTAGTGGG | 68519 |
| rs247577298 | in-del | -/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474658 | TAGGTCAAAGGTGAT[-/G]AGGTGCAGCTGATAC | 68519 |
| rs247599053 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108484840 | CCCTAAGACATGCCA[C/T]TTCCTTGTCCCTAAA | 68519 |
| rs247617062 | snp | G/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412285 | ACAAGTCCAATGTGA[G/T]ATGGGAAGTGGGGGC | 68519 |
| rs247624666 | snp | G/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108412719 | GCACTTGGGAGGCAG[G/T]GGCAGGTAGATCTCT | 68519 |
| rs247642652 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517632 | GCATCTCCCCAACCA[A/C]TCGTGAAGACCTTAA | 68519 |
| rs247659654 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108372929 | AGCCTGAGGTACACA[A/G]AGAGATTGTGTCTCA | 68519 |
| rs247669679 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108419196 | TCACTCAGCATAATG[C/T]TCTCAAAGTTCAACC | 68519 |
| rs247692487 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380431 | ACACTGTGCTGTTTA[A/G]GAAGAAATGACAATG | 68519 |
| rs247698209 | in-del | -/TCTCTCTCTCTCTC | | | intron-variant | Eml1 | Mm_Celera | 12:108480287 | GTAGACTAGATCCTT[-/TCTCTCTCTCTCTC]TCTCTCTCTCTCTCT | 68519 |
| rs247698966 | in-del | -/C | | | intron-variant, frameshift-variant | Eml1, Gm33385 | Mm_Celera | 12:108401285 | GTCTGCTGATCAGTT[-/C]CCCGGGGCTGGCTGA | 68519 |
| rs247714816 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519040 | TACCCCAATGTCAAT[A/G]AGCAGCCCCTCTCTC | 68519 |
| rs247722671 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108459933 | TGTCTGGTGTCAGCA[A/G]GGCTCTGCTCTTGAC | 68519 |
| rs247722847 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108516997 | CATTTCACCACCTGA[G/T]ACCTAGACAGCAGCC | 68519 |
| rs247744842 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108518589 | CTTGATGATGAAACC[A/G]TGCTTGAAAATAACC | 68519 |
| rs247757647 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108517299 | CCCCCTCCCTTTCCA[A/T]GATGATTTGGTATTA | 68519 |
| rs247765144 | in-del | -/TTG | | | intron-variant | Eml1 | Mm_Celera | 12:108518706 | TTGTTTAGTTGGTGT[-/TTG]TTTGTTTGTTTTAAG | 68519 |
| rs247786188 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473580 | ATCTGGGTGCAGGCC[A/G]TGCCTTCATGAGATG | 68519 |
| rs247804012 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383919 | TGCTCAGGAATCCTT[C/T]GGGGTTGTGATACTG | 68519 |
| rs247807266 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525357 | TGCGCCATCACCGCT[C/T]GGCTGGAATATATTT | 68519 |
| rs247808610 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108482411 | CGCACCACACAGCAC[G/T]CGCGCACTCGTGCAC | 68519 |
| rs247826086 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108421801 | TCTGTCTTGTTCTCC[C/T]CCCTCCAGGCTTCTT | 68519 |
| rs247834116 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108375332 | GCAAGATAATCTTTT[-/A]AAAAACTACATTTCT | 68519 |
| rs247849097 | snp | G/T | | | utr-variant-5-prime, intron-variant | Eml1 | GRCm38.p3 | 12:108422944 | GGCGGGGACCCAGGC[G/T]CGCCCAGCTCTGCGC | 68519 |
| rs247871898 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108442987 | CCTCATTAGAATGCA[A/C]ATTTGCTCTTGTTTT | 68519 |
| rs247891460 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108423836 | ATGTGTGTGGCAGGT[C/T]TTACAGGGAGGAGAC | 68519 |
| rs247909826 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469225 | AAGTGGGTGGGGTCA[C/G]GTGAACTTGATGGGC | 68519 |
| rs247927429 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108391252 | TCTCTTCACGGCCAT[C/G]TAGAGCCTCTGACCT | 68519 |
| rs247927738 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488938 | CAGGTTTCCCGTCCT[A/G]TACTTAACTCCTAAC | 68519 |
| rs247942634 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108520168 | CTGCGGTGAATGAGC[A/T]TGCTTTACTTTAGCA | 68519 |
| rs247946821 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108431842 | TTTGAAGGGTCTTCC[C/T]TATCTACTCCTCCAG | 68519 |
| rs247964589 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108476702 | AAAGCCATCTTGGTT[A/C]CCAGTACTGTAATAT | 68519 |
| rs247965375 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488016 | AGTGGTGGGCTCCAG[A/G]GCTCCCAAGCCCTCC | 68519 |
| rs247973719 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108461377 | ACTCTGATATTCTGT[A/T]AATGATATTGATGAT | 68519 |
| rs248009695 | in-del | -/CTGTGCTCAGCTA | | | intron-variant | Eml1 | Mm_Celera | 12:108395579 | GAAGAAAACCCGTGC[-/CTGTGCTCAGCTA]CTGTGCCCCGCTGCC | 68519 |
| rs248023882 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467512 | AGCCTCAGCTAGAGT[C/T]GGCACACGCACAGCC | 68519 |
| rs248081898 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108414084 | CACATCGACGCGTTG[C/T]GTAGGAATATTTTCC | 68519 |
| rs248085137 | snp | A/T | | | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108421846 | CCTCAGCCCAATCTC[A/T]TTCCCCACATGTCTG | 68519 |
| rs248094875 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108437883 | AACCTTCCCTCATCG[A/C]ACAGGTTTCTGCGAA | 68519 |
| rs248105126 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108372905 | CAGGAGGATTTCAAG[C/T]TTTAGGCCAGCCTGA | 68519 |
| rs248107072 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519236 | ATTGGGGGAATGTGC[C/T]GTATGTTGCTAGTCA | 68519 |
| rs248110539 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502449 | GTTCTTAGATTGGGG[C/G]AGGGGGCATATAATT | 68519 |
| rs248137806 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421411 | ATTCTCTGCCTTGCC[A/G]TCGCTCCGATACCAA | 68519 |
| rs248142102 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108533706 | ATGCTTCATGGACAG[G/T]GATGGCTGGTCAGCA | 68519 |
| rs248159933 | in-del | -/CCGGGAG | | | intron-variant | Eml1 | Mm_Celera | 12:108517018 | ACAGCAGCCTGTCTT[-/CCGGGAG]CCCAGGACGAGAAGC | 68519 |
| rs248178714 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108527187 | TCGTTGGGTTTGGTC[A/T]CGGGCACTTGGGATC | 68519 |
| rs248179870 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108518833 | TGGGATTAAAGGCAT[G/T]CACCACCACTGCTCA | 68519 |
| rs248224582 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108463218 | GAGGACTTGATGTAA[A/G]CAGAGTCTGATATCA | 68519 |
| rs248228489 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108518901 | CATCACTACGTGTCT[A/G]CGTTAGACACTGCTT | 68519 |
| rs248242723 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108398251 | ACTGAGGGAGGTGGG[C/T]GGATAGAGCAGTGTG | 68519 |
| rs248247838 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407235 | ACAATAGCTACTTTA[A/G]AGTTTTTGTCAAATT | 68519 |
| rs248265881 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377953 | GTGTGTGCGCGCGCG[C/T]GCGCGTGTGCGTGTG | 68519 |
| rs248267683 | in-del | -/TTA | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412967 | CTCTTTTGAGAATAT[-/TTA]TTTTTTTTCTGCTGC | 68519 |
| rs248277188 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108526704 | CCATGAACCTCAGGC[A/G]GCCTTGCTGGGTTGC | 68519 |
| rs248310508 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406230 | ACACCTTGCATTTGT[C/T]TCTCTACCAGTTCTC | 68519 |
| rs248312150 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108415149 | GCTCTGATGTTAGCC[A/G]ATCGTCTCAGTGGTC | 68519 |
| rs248313302 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471700 | TGGTCATCATTGCTG[A/G]TAGTCCCACCACTTG | 68519 |
| rs248336385 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108443665 | ACTGCCACCCGTCCC[-/TT]TTTTTTTGAAAATGC | 68519 |
| rs248349058 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108470220 | TTCTTACTGTTGAAT[A/G]TTCAGAGTTCTTACA | 68519 |
| rs248369340 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108512653 | CTCTAGTTTCAGGGG[A/T]TCTGACACTCTAATA | 68519 |
| rs248383433 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421442 | CACCTCGCCAACTTT[C/T]TACTTTCTTCTTTCA | 68519 |
| rs248383842 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469194 | CAAGCACAGGTCACG[G/T]CACTTCGCACCCACC | 68519 |
| rs248447545 | snp | A/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108537225 | AGTGGTCGCCCGCCC[A/G]GCTCTCCATTCTAAA | 68519 |
| rs248452497 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108430524 | TGCTCACATACATAC[A/C]TATAGGCACAACATC | 68519 |
| rs248453047 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108442260 | TCCAGGGTGTGTCTG[A/C]CAGCACTCACAGATG | 68519 |
| rs248480738 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108440906 | CACGGCCTGCTCCCG[C/T]CACTTCACTGCCACG | 68519 |
| rs248482448 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108475113 | TTCAAGCTTTGCTAG[A/G]ATCATCCATGGTTTA | 68519 |
| rs248488565 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380111 | CCCCTTGGAGCTGGA[A/G]TTACAGGTAGTTTTG | 68519 |
| rs248495182 | in-del | -/GCGTGTGC | | | intron-variant | Eml1 | Mm_Celera | 12:108379155 | TGTTTTGTATAGTGT[-/GCGTGTGC]GTGTGTGTGTGTGTG | 68519 |
| rs248497606 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437980 | TGGTTAGCGGGGAGC[A/G]CCTGTGGTTTGCTCT | 68519 |
| rs248500567 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108463989 | TTTCTGGAGGTTCTA[C/T]CCAGAAAGCCCACTG | 68519 |
| rs248509553 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526668 | ACTCCCAAGCCCAGG[C/T]CAGGTTGTTGCATCG | 68519 |
| rs248526730 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108420427 | TTACTTTCTTTGAGA[-/T]TTTTTCTTTCTTTTT | 68519 |
| rs248533506 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500042 | CCCCTAGAGACAAAG[-/T]TTTTTTCTATTAGGA | 68519 |
| rs248536612 | snp | A/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536606 | ACCTGGGGCCATGAT[A/T]CACAATCTCCTCAGC | 68519 |
| rs248551811 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108478011 | CAAATACAGCTGAAC[-/AG]AGAGTGGGTATCACC | 68519 |
| rs248553251 | in-del | -/GGGCGGGGACCC | | | utr-variant-5-prime, intron-variant | Eml1 | GRCm38.p3 | 12:108422927 | CCAGGGAGGGGACCA[-/GGGCGGGGACCC]GGGCGGGGACCCAGG | 68519 |
| rs248561562 | in-del | -/TTTGTTTTTGTT | | | intron-variant | Eml1 | Mm_Celera | 12:108439219 | AGTGAGTTTTAGTTG[-/TTTGTTTTTGTT]TTTGTTTTTGTTTTT | 68519 |
| rs248561592 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108427294 | GATAAAACAGTAAGA[C/T]CCAAGAGAGACTAGA | 68519 |
| rs248564483 | in-del | -/GTGTGTGTAC | | | intron-variant | Eml1 | Mm_Celera | 12:108487528 | ATAGACACAGTGTGT[-/GTGTGTGTAC]GTGTACATATACATA | 68519 |
| rs248608133 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471542 | GGGAGGAGGAGGAGC[A/T]GGGGAGGAGGAGCTG | 68519 |
| rs248609522 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372700 | TTATACTCTTTTTCT[C/T]TTCTTTGTCTGGGGG | 68519 |
| rs248618623 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108466071 | GTGAGCTGAAATAAG[C/T]CCTTTCTTCATAAGA | 68519 |
| rs248642531 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108523783 | ACACTTCATACTGGT[C/T]AAAAGAAAAATTTAC | 68519 |
| rs248643576 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108465583 | TATGTTTGAAGAGTC[G/T]GGGGAAAGAACAGAC | 68519 |
| rs248647364 | in-del | -/GTGAGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457450 | ATGCGGTATGTGTGA[-/GTGAGT]GTGTGTGAGTGTGTG | 68519 |
| rs248655448 | in-del | -/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460972 | ATAAATAAATAAATC[-/T]TTAAAAAAAAAGAAA | 68519 |
| rs248672130 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480705 | AGATATGATATGGTG[C/G]TGATAGCTCCCATTA | 68519 |
| rs248689064 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108399126 | GAAGAAACAGCCAGA[A/G]GAGTGCTTAGGAGAG | 68519 |
| rs248697594 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108425115 | TGTGAAATTAGTCAG[C/T]AGGCTTTCATGAAGT | 68519 |
| rs248701177 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530157 | GTCAATATCCTGTTC[C/T]TTTCTGTAGAGAAAG | 68519 |
| rs248707303 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473531 | ACTCTTGAGGTTCCC[G/T]CCCAAGAAGGTGGCT | 68519 |
| rs248709840 | snp | C/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410438 | GATCCATGGAGGGAG[C/G]GCACCTCTCAGGACC | 68519 |
| rs248710209 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108417942 | TGTCCCTCAGCCTCC[A/G]AAGTGCTGTCATTAT | 68519 |
| rs248712220 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108516059 | TCTGAAGGGAAGGGG[-/T]TTTTTTGTATTCCTC | 68519 |
| rs248739152 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108447672 | GCCTGCAGTGGAATG[A/G]CTTCTGATGTCCCTA | 68519 |
| rs248746523 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108472383 | CTAAAAGTGGGATTC[C/T]AGACACCTGTGTTAT | 68519 |
| rs248756791 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404952 | CGTATGCATGCACAT[A/G]CACACATGTGCACGC | 68519 |
| rs248765502 | in-del | -/ACACACAGAGGCACCCAT | | | intron-variant | Eml1 | Mm_Celera | 12:108485353 | GCCACACACACACAC[-/ACACACAGAGGCACCCAT]ACACACACACACACA | 68519 |
| rs248770459 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108516159 | GAGCTGAAAGGAACA[A/G]CTAACTTACCCAGGG | 68519 |
| rs248774690 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417510 | ACGGCACCAACAGGG[C/T]AGATCACCACACAGG | 68519 |
| rs248779939 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388519 | GTCTGGAAGGAGCGC[A/T]CATTCTTCCCTAGGT | 68519 |
| rs248785972 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524057 | AAGCAATATATATAT[-/G]ATATATACCTTCTTC | 68519 |
| rs248790520 | in-del | -/AGAGGGA | | | intron-variant | Eml1 | Mm_Celera | 12:108480101 | CCTGTGTTTCAGCCC[-/AGAGGGA]AGAGGGAAGAGCTCC | 68519 |
| rs248796097 | in-del | -/GAG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468479 | GAAGAAGAAGAAGAA[-/GAG]GAAGAGGAAGAGGAA | 68519 |
| rs248807143 | snp | A/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412817 | agagagagagagaga[A/G]agagagagagagaga | 68519 |
| rs248807416 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108515538 | ATGGCTATATAGCTG[A/T]GACATATTTGGGTCA | 68519 |
| rs248829813 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408352 | GCAATGCCACTGAAC[C/T]TCCTCTTCCCATCAA | 68519 |
| rs248838858 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456473 | AAATCTCTCCACCCA[A/G]CTCGCCAAGTTCCCT | 68519 |
| rs248849103 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108529242 | GTGGGGACAGCCACT[A/T]ATGCTTGTGGGGAGC | 68519 |
| rs248855839 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108395326 | GATCGCTCCCTCTCC[C/T]CCGCCCCAGGAGCAG | 68519 |
| rs248860244 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108506208 | GCTCAGCAGGTAAAG[C/T]CACTTACCCAAACCT | 68519 |
| rs248872673 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108528046 | CTCCAGAGGCTCTAG[-/A]AACGCTCCCAGAATT | 68519 |
| rs248880516 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494558 | AGTGTGAAGGCACTT[C/T]GTCCTGTCTTGCTCA | 68519 |
| rs248883443 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445095 | AGGGCAGCCCTGCAG[C/T]AGCAGCAAGGGTTAA | 68519 |
| rs248908466 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108372789 | GCTCTTGGAATCGTT[A/G]TGGCTGTAAAATGCA | 68519 |
| rs248947978 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108460136 | CAGGCAACTGGCATC[A/G]CCAGTGTCTCCAAAG | 68519 |
| rs248966706 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526588 | CCATTGACGTACTTA[C/T]ATGCGTTCAGGGGAA | 68519 |
| rs248975566 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108375373 | TTAGGAACTGAACAT[A/G]GGGGCAAACCACCTG | 68519 |
| rs248983975 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108459491 | TGACAGCTCAGTGCA[A/G]GGATGTCCTATAGGC | 68519 |
| rs248986543 | in-del | -/A | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536923 | AGCTGGTGTGTACTC[-/A]GGCCTCTAATATACA | 68519 |
| rs248997951 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451066 | GACAGAGACAATGCG[C/T]TTGATTGTTTATCAT | 68519 |
| rs249008459 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108392303 | GTCAGACTTCTAGGC[A/G]TGGCCTGCCTGGCTC | 68519 |
| rs249027968 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108380773 | GAATGATGATTACAT[C/T]GGTAGATGAATGGAT | 68519 |
| rs249044326 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108489094 | TGAGGTTCCCGTGCT[C/T]TTCCGCCTAGCAAGG | 68519 |
| rs249059098 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108431349 | AACAAGAGGACGAGG[A/C]TTTGGATCCTCAGCA | 68519 |
| rs249062167 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108476446 | CTGTTTTCGAGGGCT[A/C]TCTAAGTTGTAGGTG | 68519 |
| rs249072509 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108528952 | TACGGAGATGACATG[A/G]ACGGAATACTCTCCT | 68519 |
| rs249118063 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108524048 | TTTCATCCTAAAGCA[-/AT]ATATATATATATATA | 68519 |
| rs249126057 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108399099 | TCCTCACAGTTGTCC[C/T]CAGGAGCAACTGAAG | 68519 |
| rs249137994 | in-del | -/TTC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376296 | CTCCGCTTCTTCCTT[-/TTC]CTCCTCCTCTTCTTC | 68519 |
| rs249145584 | in-del | -/CTGGGCCAT | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108420859 | CAGGTTCTTACTTCA[-/CTGGGCCAT]CTTTCCGGGCCCACA | 68519 |
| rs249147820 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108533647 | GGGACTTTCCAAAGG[C/T]TGTCTAGTGAGCCTG | 68519 |
| rs249150653 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108435042 | GAATCAAAATACCCT[C/T]TTTTCTTGATAACTT | 68519 |
| rs249166670 | in-del | -/TGCCACAG | | | intron-variant | Eml1 | Mm_Celera | 12:108392240 | CTCCACCCTGCCTTC[-/TGCCACAG]TGCCACAGTGGCATG | 68519 |
| rs249170652 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376966 | CACAGTATGCAGGGG[G/T]AAACTGAGGCCAAGA | 68519 |
| rs249177440 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108496283 | TACAGTTCCGTGTCC[A/C]TTGGCCACACTTCAG | 68519 |
| rs249193553 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108425435 | GGCAGCACACAGCGA[A/C]TGGATGTCACAGGAC | 68519 |
| rs249206711 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381907 | GCTATGGGATAGTCT[A/G]TGTCGTGGCTCCAAT | 68519 |
| rs249208673 | in-del | -/TGTA | | | intron-variant | Eml1 | Mm_Celera | 12:108480219 | CATGTGAGGTGCAAG[-/TGTA]TGTGTTTATGTAATT | 68519 |
| rs249221256 | snp | A/C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376341 | ACCCTTCTCCTCCCC[A/C/G]CCTTTTTTTTTTTAA | 68519 |
| rs249251024 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432848 | GTGCCCTTTCTCAGT[A/G]ACAGAAGCCTGCAAC | 68519 |
| rs249254422 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393258 | CCTAGGGGTGGGTGT[A/G]AATTGGTCACTCCAT | 68519 |
| rs249260662 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108491388 | AACAGTGAGAACATC[G/T]AGAGGACAAATCTGT | 68519 |
| rs249278845 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108477917 | GGTCCAGGCCCTTCC[A/T]TGTATAGAGATGCCT | 68519 |
| rs249287488 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108460267 | GAAGCCGAAACTGTT[-/A]AGAGTATCACCGGGG | 68519 |
| rs249294950 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108490739 | GAAAGCACATGGCAC[C/G]ATCTGGATGTCTTCA | 68519 |
| rs249295382 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499229 | CACTCACACACCCCC[A/C/T]CCCACACACACACAT | 68519 |
| rs249296687 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108373310 | GAGTAAAAGAATCCA[A/G]AACTTGTAGCACCAT | 68519 |
| rs249303358 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502724 | GCGCTTCTCCCCGAG[A/G]GAAAGTCTCCCCTCC | 68519 |
| rs249308940 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108529371 | CAGCTCACCACCATC[C/T]ATAACTCTTGTCTTT | 68519 |
| rs249310633 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108441095 | GGATATCTTCACAGA[A/C]GATTTGGACAAGGCC | 68519 |
| rs249319350 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108484750 | ACATTTTCATCATGG[A/G]GGATGGTGACCTCCG | 68519 |
| rs249348586 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108535244 | GCAGAGACCCTCCCA[C/T]TTCAGTGAATCAAAG | 68519 |
| rs249354312 | in-del | -/TTGCTTTCTTTC | | | intron-variant | Eml1 | Mm_Celera | 12:108379641 | ATGAAGCTATTTGAG[-/TTGCTTTCTTTC]TTTCTTTCTTTCTTT | 68519 |
| rs249356541 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108397453 | AAGTCAAACAAGGTG[G/T]CTTTCTGCCTGCAAC | 68519 |
| rs249362018 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108525195 | GGCTTTGGAATATAT[-/G]TTCTTTTTTTTTTTT | 68519 |
| rs249377816 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108498253 | CGGCTGTCCCAGGGG[A/G]GTCCCCCATTGAGAA | 68519 |
| rs249378183 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108506437 | TGTTTGCTTTCGGAG[-/TT]CGCCCCGAGGCATGT | 68519 |
| rs249407208 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108445329 | ACCAAGGGTTGCAGA[-/C]CCCCATACACTGCCA | 68519 |
| rs249465080 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402355 | TGCATTGAGATACCC[A/G]AGTAATTATTGTATT | 68519 |
| rs249465180 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108394437 | ACTGGTGGGGATGCT[A/G]TGGCCTGGAGCATGT | 68519 |
| rs249476146 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108461826 | ACATGTATACATTAG[C/T]TTGTATAATATACTG | 68519 |
| rs249508706 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449953 | GTTTGTCCAGCAGCC[A/G]TTCTCTGAGAGGAGA | 68519 |
| rs249513305 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108468031 | CTACCAACAGACAGT[C/T]CAAGAATGTAGAAGT | 68519 |
| rs249572003 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500164 | AATTACAACAGGATA[G/T]TGATTATGTATTTCT | 68519 |
| rs249589593 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436387 | TAGCTCACACGCCAC[A/G]CTCTAGGAGCCTTTG | 68519 |
| rs249593826 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108481798 | CCCAACATGATCCCC[A/T]CAGCACATCAAGCCA | 68519 |
| rs249601369 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108467241 | CGAAGTCACCTCTGC[A/G]TCACTGTCACATGTA | 68519 |
| rs249623177 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532323 | TGGGTGTGAGCCACC[A/G]TGTGGTTGCTGGGAA | 68519 |
| rs249626993 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108531034 | GGTGCCTGGGCATGT[-/G]GTGGTTTATGTATGT | 68519 |
| rs249633440 | in-del | -/CCAGGAGTGG | | | intron-variant, downstream-variant-500B | Eml1, Gm33385 | Mm_Celera | 12:108400315 | GCGGTTCTAATGCCA[-/CCAGGAGTGG]CTTGAGCTACTGAAA | 68519 |
| rs249646796 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408740 | AGATGGTGCTTTACA[A/G]ATGGCTCCTGTTCCC | 68519 |
| rs249663438 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108506287 | AACTCCCAAAAGTCA[C/T]TCTTTGAGCATCACA | 68519 |
| rs249671706 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370621 | CACTTCCTGCTGGGA[A/G]CTCCTTCACACAGCT | 68519 |
| rs249681325 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488863 | AAGCTGTGCTTTTGA[A/G]CTCTCCTGGGGCTGT | 68519 |
| rs249689386 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376047 | TCATGGCTTCCTGAT[A/G]TCCCTCTGCCTAGTC | 68519 |
| rs249702805 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108505907 | TTTGCATTAGATTTT[A/T]AATTTTGATTTAATT | 68519 |
| rs249740304 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108393938 | GCAGCTCATCATTGA[C/T]CTCAGATTCCTGGTG | 68519 |
| rs249741615 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108514197 | CTGCCTTCTTGGTCC[C/T]TGTTGACATCTGGCT | 68519 |
| rs249745247 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108476288 | TCTACTCTGATGAGC[A/G]TTTGTTTGCTTGATC | 68519 |
| rs249746516 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108452276 | CTTGCTCATAGTGCC[C/T]ATGTGCCCTAAGAAG | 68519 |
| rs249762963 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413179 | TCACGGCTCTTTATG[C/T]AGCCCTGATATTGAT | 68519 |
| rs249768612 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445835 | ATATAAATCTGAATG[A/G]CAGAACTTACCAACG | 68519 |
| rs249771782 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527627 | AGTCTGAGAAGAGCA[C/G]GGCTCCGGTGGGTTT | 68519 |
| rs249772879 | in-del | -/GGA | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403742 | GGGTGTTTTGTTTTG[-/GGA]GGGGAGGGTTTATCA | 68519 |
| rs249775879 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443555 | TGCAGCGGTTGTGCT[C/T]TCCACCCATGAGGAA | 68519 |
| rs249798178 | snp | A/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404813 | ACACACACACGTGCA[A/T]GTGCAAATACACACA | 68519 |
| rs249816653 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402676 | ATAAGCTTTTCCTTC[C/T]GACCACTTTGTTCCC | 68519 |
| rs249817859 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108415580 | ATAAAAATAAATCTT[-/A]AAAAAAAAAGAAAAC | 68519 |
| rs249831723 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108521008 | GCAGTTGGTTCTGGT[A/G]TCTGTATAACTGAGC | 68519 |
| rs249841475 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451800 | TGAGCATGCTGGTAT[A/G]GTTCCTGGACATTGT | 68519 |
| rs249871716 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520157 | TCTCATTCTTCCTGC[A/G]GTGAATGAGCATGCT | 68519 |
| rs249908051 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108491074 | ACAACCCAGAGTTTG[-/A]AAAAAATCTACCCAT | 68519 |
| rs249913134 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108428995 | CCTCAGAGTGCTGGG[G/T]TTAAAGGCGTGAGGA | 68519 |
| rs249913226 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108417729 | GTGGAACAGACAGTT[A/G]CATTGTCAGGCAGGC | 68519 |
| rs249944288 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387166 | GTTCATTCTCTGCCC[C/T]TGGTACTATATTCTG | 68519 |
| rs249960447 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm33385 | Mm_Celera | 12:108400205 | GAAAGCCATGGTTCC[A/G]CAATTTGGCTTCTTT | 68519 |
| rs249980882 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108427000 | CTCTGCAAGTACACG[C/T]GCTTAACCACTAAGC | 68519 |
| rs249995907 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108398234 | TCACAGTCTTGAATA[A/C]CACTGAGGGAGGTGG | 68519 |
| rs250000403 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108417119 | ACGTAACACTGTGTC[A/G]TGGTGAACCTTAGAA | 68519 |
| rs250009178 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393685 | CTGGGAGAGAACACC[A/G]CACAGTGCTAAGCAC | 68519 |
| rs250009698 | in-del | -/TTATAAAAGG | | | intron-variant | Eml1 | Mm_Celera | 12:108448108 | TGTGGGTTTTTTTTT[-/TTATAAAAGG]AAGGTTTATTTTATT | 68519 |
| rs250039727 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522515 | GGACTTTAAGAAGGC[A/C]ATAAATAACTCCCTG | 68519 |
| rs250042165 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108497296 | CACGCCCTCCACCTG[A/C]GCCCCATTGGTCCCG | 68519 |
| rs250047562 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108476965 | GCTTGTTCAGCCTGC[-/T]TTTTTTTTTTTTTTT | 68519 |
| rs250062111 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406149 | CACAACTTTTCTTTC[C/T]CCCACTCCCCCTCCT | 68519 |
| rs250064399 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108425845 | TGTGTGTGTGTGTGT[C/G]TGTGGTGTGTGGGGC | 68519 |
| rs250065169 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108420202 | AATCCCCAAGGTTAA[A/G]AGTGTAATCATGGTC | 68519 |
| rs250067687 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108491894 | ACTAATCCACTAAGA[-/T]TTTTTTTTTAACTTT | 68519 |
| rs250074231 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504232 | TAATGAAGTGCACTG[A/G]AGGCTCTCTGGCATT | 68519 |
| rs250074269 | in-del | -/AAAAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108532730 | AAAATAAAATAAAAT[-/AAAAAA]TAAATAAAAAATGTA | 68519 |
| rs250109655 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379660 | CTTTCTTTCTTTGAT[C/T]CTATCCTTTATTATT | 68519 |
| rs250112453 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455072 | TGTGCATGTGTGTGC[A/G]TGTGTGTGTGTGCGT | 68519 |
| rs250123716 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108521833 | AAAAACTCTTCTGGG[A/G]TATATCTTTGTATGA | 68519 |
| rs250124383 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108517802 | GTATTTTAAGGATAT[A/G]CAATTTTTATTTGCC | 68519 |
| rs250128540 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530116 | GAAAACCATCAGTGC[C/T]AACTTCTGAAGAGCT | 68519 |
| rs250130696 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419383 | GATATACATGACGCT[A/G]GCATGTGTGTGGATA | 68519 |
| rs250140221 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504506 | AAATACTTGCATGCG[A/G]TGTGTGACAGTCCTT | 68519 |
| rs250140838 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461507 | CAGCTTACACTTCCA[C/T]ACTGCTGTTCATCAC | 68519 |
| rs250149751 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108529313 | TTCAGAGGACCCAGG[-/T]TTTGTCCCCTCCCGT | 68519 |
| rs250171914 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108455183 | TCCCAACATCCTTTT[A/C]TTTGGCCCACTCTGC | 68519 |
| rs250173693 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108511519 | ATTTGGTGAAATGTC[A/G]TTTCTAAAATTTAGA | 68519 |
| rs250204308 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108468060 | TTGTTCAGTCCACAA[-/G]GCTGGATGTCTAACC | 68519 |
| rs250233231 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454787 | GAAAACATGAACATG[A/C]CTTACAGATATTTCT | 68519 |
| rs250243689 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108525066 | CTAGAAACACTGATA[A/G]TCTTTTTTGTTTTTA | 68519 |
| rs250249127 | in-del | -/GG | | | intron-variant | Eml1 | Mm_Celera | 12:108433715 | TCGGCCGGCTGGGGA[-/GG]TTGGCAGGGCTTCAG | 68519 |
| rs250279354 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524355 | ATTACCATGGCCTAA[A/G]GCTGATCTTAAATAC | 68519 |
| rs250325778 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108485330 | CTCCATGCGCTATGT[C/T]CTTTGAAGCCACACA | 68519 |
| rs250336786 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108389622 | AACCCAATGCCACCA[A/G]TATGGAGAGACCAGT | 68519 |
| rs250369504 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430426 | GCTCTTCCAGAGTAC[C/T]AGGGTTCAATTCCCG | 68519 |
| rs250378285 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530632 | TGGCTGCCCTGGAAC[G/T]CACTCTGTAGACCAG | 68519 |
| rs250385373 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108416387 | CAGCCAGGGCAACTT[C/T]ATCTTTTGTTGGACA | 68519 |
| rs250416384 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376177 | CACTGGAAAAAGACT[C/T]GGGAGGTTAAGAGGT | 68519 |
| rs250416894 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108493415 | GTGGGCCACAGGCAT[A/T]CATGCAGGCAACACA | 68519 |
| rs250425661 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108526551 | ACACCTTTTTCTGAT[A/C]TCTGGGGCTTACCAG | 68519 |
| rs250470009 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108424317 | ATACACGTACTTGGG[G/T]TTTTCAGCTTATGAT | 68519 |
| rs250473491 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470289 | ACATGTATTTTCTTC[C/T]AACCTATAATTTGTG | 68519 |
| rs250483158 | in-del | -/AGACCTTTAGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108469959 | CCATTTGCCACCTGA[-/AGACCTTTAGTG]AGGTGTCTCTTCTTA | 68519 |
| rs250500050 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108418547 | GTGGAGGCATTTCCC[A/C]AACTGAAGTTCCTTG | 68519 |
| rs250501412 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532627 | TGGGAGGCAGAGGCA[A/G]GCAGATTTCTGAGTT | 68519 |
| rs250516913 | in-del | -/GTT | | | intron-variant | Eml1 | Mm_Celera | 12:108372785 | CAAGCTCTTGGAATC[-/GTT]GTTATGGCTGTAAAA | 68519 |
| rs250525330 | in-del | -/TATATG | | | intron-variant | Eml1 | Mm_Celera | 12:108425908 | ATGTGTGCATGTATA[-/TATATG]TATGTGTATATGAGG | 68519 |
| rs250542192 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108375648 | GTGGCCGCTGACCGG[A/C]TGATTGACACTCCGC | 68519 |
| rs250543190 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108469929 | GACAGTGATGTTAGC[C/T]ATCTTTTCGTGTGCC | 68519 |
| rs250558840 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108457338 | AAGCAGAAATCTGTG[C/T]TGTCCATGAGCAGAA | 68519 |
| rs250579450 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108469191 | GAGCAAGCACAGGTC[A/T]CGTCACTTCGCACCC | 68519 |
| rs250591125 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442437 | CTGGTTTACTGAAAA[C/T]GAAGATTCACGGTCC | 68519 |
| rs250602729 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108416792 | TCATCATCACCACCA[C/T]CACCATCAATATCAA | 68519 |
| rs250646667 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442146 | GTGGTTCCAACCCCA[C/T]GTGGCATTGCGTGAC | 68519 |
| rs250647141 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379209 | TATGTGGGTACAGAT[C/G]ATGTGTGTTTATGCA | 68519 |
| rs250657089 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380634 | CTGGAGTTGGTCCCC[A/G]CCTCGGAGATTGTTT | 68519 |
| rs250658126 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469006 | AGAAGGATGTGACAG[C/T]CAGGATGGTAAGGAC | 68519 |
| rs250683291 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108514663 | TTGGGGTTCCCCGTA[C/T]AGTTGGGAAGTCCTC | 68519 |
| rs250694919 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447627 | GAGAGAGATGTCTGA[C/T]AGTCTTAATGCCAGG | 68519 |
| rs250700895 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108475851 | TGGGTCTCTAGGATG[A/G]AACTCCATCCATCAC | 68519 |
| rs250716149 | in-del | -/ACACACACAC | | | intron-variant | Eml1 | Mm_Celera | 12:108497523 | TTGCCTTTGGCCAAT[-/ACACACACAC]ACACACACACACACA | 68519 |
| rs250719084 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108521590 | CATGAGACGGTCCTT[C/T]GGGGGTGCCGTTGTG | 68519 |
| rs250728516 | in-del | -/GGGA | | | intron-variant | Eml1 | Mm_Celera | 12:108372296 | ATGCCAGACTGTCCC[-/GGGA]GGGAGGCCCTGTGGT | 68519 |
| rs250746749 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404750 | CAAATACACACACGC[A/G]CACATGAACACACAC | 68519 |
| rs250755920 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108509765 | CCCTGCCTCGAAAAA[A/T]GAAAACGTGCTTTGC | 68519 |
| rs250791072 | in-del | -/GTGC | | | intron-variant | Eml1 | Mm_Celera | 12:108482422 | CACTCGCGCACTCGT[-/GTGC]GCACACACACACACA | 68519 |
| rs250791428 | in-del | -/GCCAGGT | | | intron-variant | Eml1 | Mm_Celera | 12:108396629 | TCTCAGGTATAGGTG[-/GCCAGGT]GCTACAGAATCAGTG | 68519 |
| rs250809188 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503032 | TAATTACCACAAACC[C/T]ACAGGCATGCAACCT | 68519 |
| rs250855809 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108448895 | AAATCATCTTAGAGC[C/T]AAGGATGGCCTTGAT | 68519 |
| rs250872617 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478044 | ACAGATGTCAAGGAG[C/T]CGGGGTTATTAGGTA | 68519 |
| rs250885606 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108509561 | GTGGGCGGGGCCGGG[C/G]CGGGGCGCAGTAATT | 68519 |
| rs250930286 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108420599 | ACTTGTTCTGTAGAG[C/T]ACTAGCCTGGCCTTG | 68519 |
| rs250967494 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108384001 | GGACCCTGCCTCAGA[A/G]CTCACCCATCATAAA | 68519 |
| rs250973577 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108479912 | TTGGATTTTGTTGAT[C/T]TGTTTTAGGAAACCA | 68519 |
| rs250987052 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108444792 | GAGAGTACAGCTGAA[A/G]AGGTCTTCTTCTTTG | 68519 |
| rs250988418 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372050 | GGCTACACACCTACC[A/G]TGCGGTTTGCGAAAA | 68519 |
| rs251008570 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479470 | ATACTGGTCTCTATT[G/T]TTCCTTTACCTTTTA | 68519 |
| rs251031294 | in-del | -/GGGTTTTTTTTTTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108432024 | TAAAATGTCAACATC[-/GGGTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 68519 |
| rs251037434 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108383107 | CTAGGCAAGAGGCTC[A/G]GAGCTCATTAACTCT | 68519 |
| rs251042436 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108391326 | ATCCTGACAGAACCT[A/G]AATCATCCGGGAGAC | 68519 |
| rs251044861 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108444013 | TGTATGGTACTTAAA[A/T]TTTTAATTGGCAGTT | 68519 |
| rs251047270 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450996 | AGGAGACCCCAAACA[A/G]TAAATGACCAGGGGA | 68519 |
| rs251075745 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486416 | TCTGCACCAGTGGCA[A/G]CCTGGTGCCTTCTCT | 68519 |
| rs251086153 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108450195 | GTTCAGACGTCAGCA[C/T]TGTGACATAGGAAAT | 68519 |
| rs251087790 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108508797 | TAAAATTTGTCTTTA[-/G]GTATGTAGGTACTGA | 68519 |
| rs251093497 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378308 | TCATGAGAATGGCCT[C/T]TTGGGTGTCACTGAC | 68519 |
| rs251098650 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440371 | AGGACACGGAGACAT[A/T]CAAGTCCGAGAACTG | 68519 |
| rs251151983 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108428511 | GAATTTCCTTTGTAG[A/G]CTGTGCTCTCTCAAA | 68519 |
| rs251156038 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108485985 | CACCACAGGATGAGT[C/T]GCACACTTGTGCATA | 68519 |
| rs251185847 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108462042 | CTAGAGTTGCTATAC[A/G]TGGTAATACCTGTTT | 68519 |
| rs251196733 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108512750 | TGGCGCACACCTTTA[A/G]TTCCAGCACTGGGGA | 68519 |
| rs251205673 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108472400 | GACACCTGTGTTATC[G/T]TTAGAGAGATCACAG | 68519 |
| rs251224804 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469029 | GTAAGGACAAGAGGA[C/T]AACCAAGGCTGACAG | 68519 |
| rs251228706 | in-del | -/TTC | | | intron-variant | Eml1 | Mm_Celera | 12:108526154 | ACAGGGGAAACAGAT[-/TTC]TTATCAGAGAGTCAA | 68519 |
| rs251230187 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108424094 | TTACAGAATTTTCTC[C/G]AGTGCAGTCAGGATA | 68519 |
| rs251231182 | in-del | -/CCTGT | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108400862 | AAATGGCCCTGCACA[-/CCTGT]CCTGTGTTCAGCCCT | 68519 |
| rs251246516 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108396137 | AAGTGAGTTTCAGAG[C/T]CCAGTAGTGATGTTG | 68519 |
| rs251252257 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108499287 | GGATCCACATTTGAG[A/T]GAATGTGTGTGCTGG | 68519 |
| rs251267064 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108434602 | AGGAATGCCAGAAGG[A/G]AGGGACACACACCAC | 68519 |
| rs251269327 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479686 | TATGATTCGTTCTTA[C/T]TAGGTTATATAGTTC | 68519 |
| rs251278726 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532062 | TTCTGACTTAAACCT[C/T]CCATTCCTAAGGGCC | 68519 |
| rs251290283 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519601 | GCCCACTTCCTTCTG[A/T]AAACCCAGGGCTGGG | 68519 |
| rs251299827 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108488042 | CTCCTACAGTATATT[-/G]GGGGGTCTTTGGCTC | 68519 |
| rs251335101 | in-del | -/AAGC | | | intron-variant | Eml1 | Mm_Celera | 12:108436940 | GCCATTTAAAGAGAT[-/AAGC]AAGCAAAAGCTGCGC | 68519 |
| rs251369401 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108531394 | GTGTGGTTGTGCACA[C/T]CTGTAGTCCCAGCAC | 68519 |
| rs251376333 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108501425 | GGACATGTGGCTGGT[A/T]CTAGCCCTTCTGTTG | 68519 |
| rs251378137 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108386017 | TCGCTTAGGGCAATG[C/T]CAGAGTCAGGACATC | 68519 |
| rs251384998 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404875 | ACACACACACATGCA[C/T]ATGCAAATACACACA | 68519 |
| rs251387293 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108398329 | GCCCGGCTGCCCTTT[A/G]TCTGCCGAAGCCAAG | 68519 |
| rs251395826 | in-del | -/TTATT | | | intron-variant | Eml1 | Mm_Celera | 12:108426485 | CCATCTCACCAACCA[-/TTATT]TTATTTTATTTATTT | 68519 |
| rs251399335 | snp | A/G | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108370411 | GGTCCCAGGGGCGGG[A/G]GGATAAGACAGGGAG | 68519 |
| rs251403302 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108455355 | CTGTTCTAGTTGAGA[-/C]CCCCTAACCTTGCCA | 68519 |
| rs251403780 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108481608 | GGTGGGGGAGGCGGC[A/G]GAGATATAGTCTATA | 68519 |
| rs251404171 | snp | G/T | | | intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538008 | GAGCTTACAAGGGGG[G/T]CAGTAACGGAGTTTT | 68519 |
| rs251419992 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108373819 | GGCCTTAGGCCTGGG[C/T]GGGCAAGCCTACAGG | 68519 |
| rs251428648 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392774 | TAAACCTAACCGGCT[G/T]CAATCTCACTAATGG | 68519 |
| rs251452508 | snp | A/C | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369471 | GCCTTTGAAGTTTTG[A/C]ATTCCTTTGCTAGTT | 68519 |
| rs251455344 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442784 | TGGCTTAAGACTAGG[A/G]CAGAATGTCAAACAG | 68519 |
| rs251456878 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503520 | CTCCCCACAAGCACG[C/T]ACCTCTGGGTTTGGT | 68519 |
| rs251459755 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108387931 | AGATGGTTGGTAGAT[-/G]GTCTGCTGAATGTTT | 68519 |
| rs251483128 | in-del | -/TTTTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108436835 | CTCTCTTTCTCTGTC[-/TTTTTT]TTTTTTTTTTTTTTT | 68519 |
| rs251495213 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108471279 | GAACAGGAGAAGGAT[C/T]AGCAGGAACTGAGGA | 68519 |
| rs251530720 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464623 | CTAAGACAGTCAGGA[C/T]TACACAGAGAGACCC | 68519 |
| rs251563730 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108509278 | ACATAGGTGAACTAG[C/T]CTTAGCCAAAAGAAT | 68519 |
| rs251575078 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381201 | GGGGCATGGAGGACC[A/G]TGGACAAGAGAACAG | 68519 |
| rs251577190 | snp | C/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478355 | TATTTTTTTAAGAAT[C/G/T]TTTAAAGATTTCTTT | 68519 |
| rs251577343 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108470811 | TGGGTAGGATGTCTC[C/G]AATGCTCTGAGAGGG | 68519 |
| rs251586689 | in-del | -/GGGG | | | intron-variant | Eml1 | Mm_Celera | 12:108535385 | AGCGGAGGGGGTCGT[-/GGGG]GGGGGGGGAGTGGGA | 68519 |
| rs251598198 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108508466 | GTACTTGTATCATTT[C/T]AAAGTGATGTTTAAT | 68519 |
| rs251624036 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474309 | GTGAGTTCCAGGACA[A/G]CCAGGGCAATACAGA | 68519 |
| rs251626332 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108498177 | CGTGGACCAAGCTTC[C/T]AGCTGGTGGCCCTTT | 68519 |
| rs251637199 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108387482 | GTCACCTTGAAGGTT[A/G]AAATCTAATCCCACC | 68519 |
| rs251641401 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108534537 | TGAAAAACAATGTTT[A/T]CCCAATGTTTTCCTT | 68519 |
| rs251644438 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108438153 | TTGTTGTGTGAGGGA[G/T]GGAGTAACCCTCCTG | 68519 |
| rs251652371 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108526026 | CCCCGTGAATATCCC[A/G]TGTCCTGTGACGGCA | 68519 |
| rs251652895 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108438549 | CTCAAATCTTCTCAC[A/G]TAGCTTTTAGAACCC | 68519 |
| rs251672222 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108535579 | CAACCTTATGAATAG[-/A]AAGTTCAGATGCCAG | 68519 |
| rs251674609 | in-del | -/GGA | | | intron-variant | Eml1 | Mm_Celera | 12:108489529 | AAGAGGAGGAAGGAG[-/GGA]GGAGGAGGAGAGCTG | 68519 |
| rs251676589 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504648 | GATTCTGGATTCTCC[A/G]ATCTGCGAGAACATC | 68519 |
| rs251687695 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405594 | TCATGTGACAACCTT[A/G]GGTGGCATCCTTCTG | 68519 |
| rs251692152 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108401759 | TTATTGAGATGAGCA[G/T]GAAAACTGCATTCTT | 68519 |
| rs251696895 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466243 | GTTGGAGCTTAGACA[-/G]GGTATTGGCATATCC | 68519 |
| rs251700894 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108484162 | AATTTGTAGAAACCT[A/T]CCAGATCTGCAGAAC | 68519 |
| rs251705960 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108443808 | CCATAAATCCTAAGG[A/G]ACATATTCTGGGTGA | 68519 |
| rs251728813 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108533991 | AGCACTACCACCCAG[C/T]AGCCCAGACTTCCTT | 68519 |
| rs251730040 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108492116 | ACTGTTGGAATCTTT[C/G]TTACCACATACATAT | 68519 |
| rs251752666 | snp | G/T | | | intron-variant, missense | Eml1, Gm33385 | Mm_Celera | 12:108401337 | GCTTTGAGCTCCGAG[G/T]CATCACGTGGCACTT | 68519 |
| rs251762977 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532121 | TTTAGTAACCTTCCG[A/G]CAGAATTCACGTGAA | 68519 |
| rs251764435 | snp | C/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413624 | TTATTGAATGTGTAT[C/G]GTTATTTTGTCTGCC | 68519 |
| rs251806853 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407873 | GGGATCAGCCAGAGG[A/G]TCTGGCAGGACTCAC | 68519 |
| rs251815892 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108374314 | AGACACTTACCTGAT[A/G]GGTGAACATTTGTCC | 68519 |
| rs251854532 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108505708 | TAAAGTGGGTTTCTC[A/G]ATTACTTGTGATTCT | 68519 |
| rs251861188 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407335 | TTTCCTGCAGAGAGG[A/G]GAGAAAAGAGGTGAG | 68519 |
| rs251862186 | snp | A/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406556 | CAGCCCTGTGTGCTC[A/T]TGTACTAGTTAGCAC | 68519 |
| rs251899316 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108373555 | TCGTCTGCTGTAGGG[A/T]CTAGCAGAGGCTGGA | 68519 |
| rs251903844 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108447187 | TTGAGAGAGCCAAGT[A/G]CCTTCTAACACAGGG | 68519 |
| rs251917178 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504825 | ATATCCATTTATTAG[A/G]ATACCGAAGTATTTT | 68519 |
| rs251923291 | in-del | -/CA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473133 | ATACACACACCACAC[-/CA]CACACACACCAAGCG | 68519 |
| rs251943751 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390711 | GGAGAGGGGTCTGCA[C/T]ACACCACAGTACACA | 68519 |
| rs251948359 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108512129 | AATCCTAAAACAGCC[A/G]TGGGCCTGGCCAGGA | 68519 |
| rs251960227 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108506934 | TAGTCAGGGTTTGTA[G/T]TCCTGCACAAACATC | 68519 |
| rs251962096 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474766 | AACATCCCGCCCTTC[A/C]CCAGGCAGATTCTCC | 68519 |
| rs251962798 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108441831 | TCCTGAGCATGCATG[C/T]GCAGGCCCCTGTGTG | 68519 |
| rs251982612 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108525830 | AAAACAAAACAAAAC[-/A]AAACAAACAAAAAAA | 68519 |
| rs252008485 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108458287 | CAGAGTCACCGCTCC[A/G]AGGACAGAACCCAGC | 68519 |
| rs252008582 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451078 | GCGTTTGATTGTTTA[C/T]CATGTAGATATTTAG | 68519 |
| rs252017466 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447293 | GCCATCTTTGTTAAA[A/G]CGAGGATGAGTGGAT | 68519 |
| rs252025503 | in-del | -/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409521 | TCAAAGATTTTTTTT[-/G]GTAAGATCCTGACTC | 68519 |
| rs252045529 | in-del | -/TTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108439424 | CTAGTCCATAGCAAC[-/TTTT]TTAAAAAAAAAAAAA | 68519 |
| rs252048877 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474249 | CAGCACTCGGAAGGC[A/C]GAGGCAGGAGGATTT | 68519 |
| rs252087080 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402867 | TCCAGCATCCCGGGC[A/G]AAGCTCTCCATCTAA | 68519 |
| rs252133527 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108375980 | GACACTGTTCTTAGA[C/G]GGTGGTCTCTGGGCC | 68519 |
| rs252136990 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404939 | ACGCACGTGCACACG[C/T]ATGCATGCACATACA | 68519 |
| rs252139869 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384435 | CAGGACTGGAATGAT[A/G]TTGCCTGCCACCCCT | 68519 |
| rs252169554 | in-del | -/CCAAC | | | intron-variant | Eml1 | Mm_Celera | 12:108432158 | ACTTGGCTGATCTTT[-/CCAAC]CCACTCACTGCCCGC | 68519 |
| rs252183173 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412061 | CAGGCATGCTCTAGG[C/T]GTGATGGTGCAATCC | 68519 |
| rs252190863 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108519825 | GAGTGCTGGGATTAA[-/AT]AGGCGTGCTCTGCCA | 68519 |
| rs252199717 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108432999 | TGATTTATGCTCTTC[C/T]CAGTTTGGTTCTCTG | 68519 |
| rs252215931 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372107 | TGGTGTCAGTGTATC[A/G]TGAGTGCAGCGGTTC | 68519 |
| rs252218266 | snp | A/C/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381131 | AGCTCAGGGAGAGGG[A/C/G/T]TGGGGGAGAGGGGCG | 68519 |
| rs252228091 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108502070 | ATGTGAGTTCAGATC[C/T]CAAAGCCACACAAAA | 68519 |
| rs252230601 | in-del | -/TA | | | intron-variant | Eml1 | Mm_Celera | 12:108478340 | TTTTTTTTTAAGATT[-/TA]TTTTTTTAAGAATGT | 68519 |
| rs252231385 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108513107 | TGATGTCCCACAGGG[C/T]ACTGCCTGCACAGCC | 68519 |
| rs252243828 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419092 | TCCCAGTGTCCATCT[A/G]TCATTTCTGCTCCAT | 68519 |
| rs252248150 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430981 | TGGCTGAAGGCCCAG[C/T]CCACCACGACCCAAG | 68519 |
| rs252249869 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108385131 | CTACTGCAGGACCTT[A/G]GGGGGAAAAGAAGCC | 68519 |
| rs252252483 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402179 | ATTATGGTTTGGCTG[A/G]TACATTATTTAAAAG | 68519 |
| rs252253014 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108439516 | TCTCATTATGGATGG[C/T]TGAGTGCCACCATGT | 68519 |
| rs252254194 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465003 | TTTGTTTGTTTTTGG[G/T]TTTTTTGTTGTTGTT | 68519 |
| rs252268060 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108527984 | GCCGGATCTGTCAAC[A/C]CGTCTCCTCCCCAGC | 68519 |
| rs252282728 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108393625 | TTGTATACCAAAGGT[C/T]CTTACCTATGCTGCC | 68519 |
| rs252294831 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108432186 | TGCCCGCCAGTGGGC[A/C/T]GGAGGCAGGAAGGAC | 68519 |
| rs252300030 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108497376 | CACCAGCAATCCTTG[C/T]TCTCTCAGGCAGTCT | 68519 |
| rs252301337 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108527314 | GTTTATCTAGTAGCA[C/T]CTCTGTGGCTCCAAT | 68519 |
| rs252309741 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438787 | TCTGTATTGGGGGGT[G/T]TTGGGGGAGAAATGA | 68519 |
| rs252312869 | in-del | -/ACCA | | | intron-variant | Eml1 | Mm_Celera | 12:108397551 | TACCATCTCCCTCCT[-/ACCA]TCATTAGTTCTGTGT | 68519 |
| rs252336669 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108399909 | GGTAAGTTAGGCACT[-/G]GCTCACAAGAGTGTC | 68519 |
| rs252348968 | in-del | -/AAAAAAAAAAAAAAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108535529 | CCCTTTGTATCGATT[-/AAAAAAAAAAAAAAAA]AAAAAAAAAAACAAG | 68519 |
| rs252356106 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108476834 | TTGCTATGATAAAAA[C/G]CATGAGGCAACTTGG | 68519 |
| rs252368123 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460827 | GGCTCAGTGAATAAG[A/C]GCACTGACTGTTCTT | 68519 |
| rs252400047 | snp | C/T | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | GRCm38.p3 | 12:108400685 | GGACCTGTATTAAAC[C/T]GTCATAGTCTCAGGA | 68519 |
| rs252416316 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108516698 | GGGGGGGGGGGGGGG[A/G]AATAGATGAATTTTA | 68519 |
| rs252440433 | snp | C/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413607 | AAAAAGATTTATCTA[C/G]TTTATTGAATGTGTA | 68519 |
| rs252473330 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108466185 | TTCTTGTTCCTAACC[C/T]TCTCAGTGACACACG | 68519 |
| rs252501833 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108465686 | TCACGGTGACCTAAC[A/G]CCTCGCTGTGTGCCG | 68519 |
| rs252508530 | in-del | -/AT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472988 | ACACACACACCCCAC[-/AT]ACCATACACACACAT | 68519 |
| rs252510958 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108420958 | TAAAGGTTAGGAGGG[A/G]AGCAGGGGAAATGAA | 68519 |
| rs252513680 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108428231 | GTCAGAGCTTTTCTT[C/T]TGGGGAGTAAGTTCT | 68519 |
| rs252515023 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108464855 | CTTCAGGCCAATGGG[A/T]GATCTTGTGTTTAAA | 68519 |
| rs252540634 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108465002 | TTTGTTTGTTTTTGG[-/TT]TTTTTTTGTTGTTGT | 68519 |
| rs252550191 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108436002 | TCAGAGACAAGAGTT[C/T]ATCCAGGACCTGTCC | 68519 |
| rs252558903 | in-del | -/AC | | | intron-variant | Eml1 | Mm_Celera | 12:108485433 | CATGCACACACACAT[-/AC]ACACACACACACATA | 68519 |
| rs252559383 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108397366 | GGGCTCCTTCCTTCT[-/G]TCCTTCCTTCACTGC | 68519 |
| rs252567370 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108434400 | CACCTGGTGAGCTGC[C/T]ACAGGTCTTGGTACA | 68519 |
| rs252571161 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518269 | ACATACATGCAGACA[A/G]ACATTCAGATATATA | 68519 |
| rs252583360 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108475172 | TCTGATGGTGGGAGG[C/T]GGTGCTTTGACTCTC | 68519 |
| rs252594675 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108435345 | AACCACTTGTACTTT[C/T]AGAAGTTTCTGAACA | 68519 |
| rs252599209 | in-del | -/AC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473250 | ACACACCAATCATAG[-/AC]ACACACACACACATA | 68519 |
| rs252603045 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108435201 | CCTTACTTATGTCTG[A/C]ATTCTAAGATGTCTT | 68519 |
| rs252611812 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440940 | AGGCTTAGGAATATG[-/T]TGCTGAACTTTTTCA | 68519 |
| rs252631994 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441617 | GCCCAAGGCTCACCT[C/T]AGACATCTTGAGTTC | 68519 |
| rs252639117 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437354 | CACCTGGTGCAGAAG[A/G]CCCAGTCCAGGCCTG | 68519 |
| rs252643042 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437158 | ATTTTTCCTGATCTC[A/G]CAATTCTTGTCTAGA | 68519 |
| rs252658062 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108426414 | CTTCCACCATGTGGA[C/G]ACCAGGGATGAAGCA | 68519 |
| rs252668863 | snp | A/C/G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530182 | AGAAAGCTGTGGGGG[A/C/G/T]GGGGGTTTCTTGAGT | 68519 |
| rs252695116 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108526082 | CTGAGAATATGCAGC[C/T]TCATCTCTCCCTCTC | 68519 |
| rs252708887 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380079 | GGGGTGCCTAAGGCA[A/G]CCAGGAAAGTGTCAG | 68519 |
| rs252712844 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384703 | GCTAGTTAGATAGTT[A/G]TCAGGAGAGTGTCTA | 68519 |
| rs252730113 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468596 | AAGAAGAAGAAGAAG[A/G]AGGAAGAAGAAGAAG | 68519 |
| rs252738942 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482628 | TTCGGAAGAGCAGTC[A/C]GTGTTCTTATCCGCT | 68519 |
| rs252769496 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | GRCm38.p3 | 12:108536121 | AGCTGTGTACACTGT[A/G]CCCATGGGAAGGTGG | 68519 |
| rs252775377 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108492777 | AGCATTCTTAACAAT[A/G]CTAAGGCACGCAGTA | 68519 |
| rs252789861 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450875 | CGGACTTTGAAAGTA[A/G]CGTACACATGAGGTT | 68519 |
| rs252791116 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108478256 | TGTGACAAACAACAC[A/G]CGTTCACCCAGGACT | 68519 |
| rs252792686 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402986 | CTGTCTTAGCTCATT[A/G]GCCATAAGCATTTTT | 68519 |
| rs252797491 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482084 | TAAGACTTTCCAAGT[C/G]GCTTTTTCTGGGAAA | 68519 |
| rs252813644 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108500572 | AGCTTGCCCCAAGCC[A/G]ACTCTTCTTGCTTCT | 68519 |
| rs252822421 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489372 | AGAAGGGGGATGGGG[A/G]GGAGGTGGTGAAGAA | 68519 |
| rs252830537 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429953 | TCCAAGCCTCGCGCG[C/T]TCTGAAGGCGTTCCC | 68519 |
| rs252844939 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108492074 | TCTGGCAGTGAGTTG[-/C]GTTTGTAGAGTAAGA | 68519 |
| rs252863280 | in-del | -/GTGAGTGTGTGTGTGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475734 | AGTGTGCCTGAGTGA[-/GTGAGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs252863910 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108529918 | TAGCCGGGAGTCACA[A/G]CCATGGCCTGTGAGC | 68519 |
| rs252891469 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454701 | ACTATGTAGACCGAG[C/T]TGGCCTGGAACTCAC | 68519 |
| rs252935562 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108382889 | CTGGGGGCCAAAAGC[C/T]GATGGCCTCTAGAAA | 68519 |
| rs252935660 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108523778 | GAAGGACACTTCATA[C/G]TGGTTAAAAGAAAAA | 68519 |
| rs252966100 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108397213 | GTTGTGGGCTGGGCT[C/T]AAACCATTCTATTGG | 68519 |
| rs253001661 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485892 | TTTTCTCATTTTCTT[C/T]CCTCTTTCCTGCCTG | 68519 |
| rs253037961 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108453944 | CAAGCTGTTCACAGT[A/G]AGAGGATGTGTGGTT | 68519 |
| rs253062409 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108493603 | AGGGAGATGGTCCCC[C/T]CAGGCGATGCTAGAT | 68519 |
| rs253062734 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485024 | CTGTTACTTGGAGTA[C/T]ACTTCCTCACTCTAA | 68519 |
| rs253063430 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108423811 | GATTTGTTTTTCCCT[A/G]TATGTGACTATGTGT | 68519 |
| rs253070601 | in-del | -/AAACA | | | intron-variant | Eml1 | Mm_Celera | 12:108525805 | AGAAACCCTGTCTTG[-/AAACA]AAACAAAACAAAACA | 68519 |
| rs253073175 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108469716 | AGATCATATGGTAAG[A/T]TTATATTTAGCTTTA | 68519 |
| rs253084715 | in-del | -/CCC | | | intron-variant | Eml1 | Mm_Celera | 12:108388991 | CTGAACTCTGACCTT[-/CCC]CATGCTTGGGTGGTA | 68519 |
| rs253094476 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520881 | AGGTCCTAGGTTCTA[C/T]CCCTAGCACTACTAT | 68519 |
| rs253096573 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374504 | AGAGATGGCTGCTCT[G/T]GATACTCTCGTTGGG | 68519 |
| rs253132447 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108453542 | CTGCGATTCAACTCC[A/G]GTTCTTCTGCTTATA | 68519 |
| rs253148638 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108378681 | ATTTCCCTGTTGTTT[-/C]CCCCCTTCAACATTT | 68519 |
| rs253163717 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108459645 | ATTCCTTGACCTTTC[A/G]AATAGGATGAAAAAA | 68519 |
| rs253164059 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108452421 | GGGCCTCACTACCTC[A/G]TAGTTTTACTGTTTA | 68519 |
| rs253169983 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108476939 | AGGCCATAGAGGAAT[A/G]TTGTTTACTGGCTTG | 68519 |
| rs253258861 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108428976 | AGAGATCTGCCTGCC[C/T]CTGCCTCAGAGTGCT | 68519 |
| rs253279787 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108450738 | AAGTCTAAAGCTGGG[A/C]AAGAAGCCAGCGAGT | 68519 |
| rs253282714 | in-del | -/TTTTG | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403222 | GTTGTTTTTTTTGTT[-/TTTTG]TTTTGTTTTGTTTTG | 68519 |
| rs253283003 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108484451 | AAGTGTCCAGTTCCC[A/G]CTGGCTCTTCCCATC | 68519 |
| rs253311777 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108426753 | TAACCATTAGCAATT[A/G]GTACCCTAGCCCCTG | 68519 |
| rs253315839 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108483776 | ACTGGAGCTGAGGAG[A/C]TGGCTCGGTGGTTTA | 68519 |
| rs253345312 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108389394 | CTAAGTCCGCATTTG[C/T]GGCCTCTGTCCTATA | 68519 |
| rs253355342 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471142 | CGGGTTTGATCCGCA[C/T]GCAATGCTGTGAGAG | 68519 |
| rs253363901 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108522312 | TCACAGGAAGGGCAG[A/G]CTCCAGTAAGATATA | 68519 |
| rs253373054 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108440808 | GGTAGCTCTTCTCGG[A/G]CCTGGTGGAGCTTGG | 68519 |
| rs253376393 | in-del | -/C | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370603 | TGAGCACAGAAGTTA[-/C]CTCACTTCCTGCTGG | 68519 |
| rs253444351 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402642 | TAAGGTGGTAAAATA[C/T]GTAGCCGCACTTGTA | 68519 |
| rs253449242 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108428874 | gttttttatttgttt[A/G]tttgtttgtttgttt | 68519 |
| rs253455260 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108418265 | GAACAAACATCATGA[C/T]CAAGAAGCAGGTTGG | 68519 |
| rs253455352 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410895 | GGACCAGGCTCGGTG[C/T]CTGTCTTCTGCTCCG | 68519 |
| rs253459734 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108457059 | CCTCTATTCATTCAG[G/T]GGAGGGTTCACAAGA | 68519 |
| rs253492221 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455678 | AGCTTGGTGTCTTCT[C/G]CTCTGGGTTGGATCT | 68519 |
| rs253526572 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462189 | GATGGATCATCAGCA[G/T]GACCCATGTGGTAGG | 68519 |
| rs253530641 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108394957 | ATGCGTATACACTGA[A/G]AATTCTCACACATGT | 68519 |
| rs253547537 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108444695 | CTGAGGACATTCGTG[G/T]GGCTGTACCTTTGTG | 68519 |
| rs253555707 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108515754 | TCTCAGTATAGCCCT[A/G]GCTGTCCTGGAGCTC | 68519 |
| rs253556602 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524318 | TACAAGAAGAATGAA[A/G]TCATCCCATGCATCC | 68519 |
| rs253576777 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499522 | AGCCATGTGGAGCAA[G/T]CCAGTAAGCAGCACC | 68519 |
| rs253581554 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108421722 | AGGTCACACCCAACC[C/T]CAGCCCTCTAACCCA | 68519 |
| rs253603551 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108461858 | AAGTGAAGCAGATAC[A/G]GAACCCATCGACTGT | 68519 |
| rs253620284 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108467586 | GGAAAGAATAAGATC[C/T]GAATGTTTATGCTTT | 68519 |
| rs253624984 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108386765 | TGGCCACCCGGAGAC[-/T]TTGCTGCAGTGGCTT | 68519 |
| rs253628492 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402580 | CTTTTGCCTAGGAGG[C/T]GAGCACTCTGCAAAC | 68519 |
| rs253632357 | snp | C/T | | | utr-variant-5-prime, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410684 | GATGGGAAGAGGAGC[C/T]GGCTGGCTGAGGTGA | 68519 |
| rs253634707 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530677 | CCTAGAGATTCCCCC[-/T]GCCTCCACCTCTCAA | 68519 |
| rs253641414 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108418058 | AGATTCTCTGATGAC[-/TG]TGTGTCTGTTTGATA | 68519 |
| rs253644476 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108430771 | ACCCCAGGTAGACAC[A/G]CTTCTGGCTTTATTT | 68519 |
| rs253648006 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108460152 | CCAGTGTCTCCAAAG[A/G]TCAGGCTTTGCTCTC | 68519 |
| rs253648874 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108384719 | TCAGGAGAGTGTCTA[C/T]GGTGCAAGCATGGGG | 68519 |
| rs253665388 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442590 | AGAAGAGGGTGTCAG[A/G]TCCCATTACAGATGG | 68519 |
| rs253668656 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108425849 | TGTGTGTGTGTCTGT[-/G]GTGTGTGGGGCAGTG | 68519 |
| rs253676561 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108505486 | CCACAAAAAACACAC[-/A]AAAAAGTCTTATTTA | 68519 |
| rs253681635 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108526878 | TCACAGCTGAGCACC[A/G]GCACTGAGGGTAGGC | 68519 |
| rs253684359 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108507622 | AGGTATGAGCTTACG[C/G]TCCCCTAAAGAGCTA | 68519 |
| rs253691820 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108409576 | CTCTGTCTCTCTGTC[A/G]CACACAAACACAAAC | 68519 |
| rs253720915 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442318 | GGTTAGGAGCACACA[C/T]GGGCGTGTCTGCCGT | 68519 |
| rs253728088 | in-del | -/CT | | | intron-variant | Eml1 | Mm_Celera | 12:108475578 | GCCCTAGGGATGGCA[-/CT]CTGCTCTCAGCTTGG | 68519 |
| rs253731791 | in-del | -/AA | | | intron-variant | Eml1 | Mm_Celera | 12:108506357 | AATAAATGCATCTTT[-/AA]AAAAAAATGTAAGGT | 68519 |
| rs253750954 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108533036 | CACTGGTGGGTTTTC[A/T]TACTATTTTTCTGTC | 68519 |
| rs253765511 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507117 | CCCCTGGCTTGCTCA[A/G]CCTGCTTTCATATAG | 68519 |
| rs253785524 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447833 | GGGCACTCCTGGTAC[C/T]GAGGTAAAGATACAG | 68519 |
| rs253791427 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392045 | TGGGCTTCAGTGGAC[C/T]GATTTGTAAATGGGA | 68519 |
| rs253799627 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108514932 | CCATTGAGTTGTCCG[A/G]AATTTCTTTCTCCTA | 68519 |
| rs253820508 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108481225 | TAGGGGTAAGGGGGT[G/T]TGGGTGGGTGGGTGG | 68519 |
| rs253823771 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108377362 | TCTCCTTCTGGATTC[-/A]GGGTAAGTTATGTGT | 68519 |
| rs253841280 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376436 | CAGATCTCATTACGG[A/G]TGGCTGTGAGCCACC | 68519 |
| rs253851484 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447879 | TCATCACCAGGTGCC[C/T]TGCGGGCCAGGTGAG | 68519 |
| rs253876623 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524360 | CATGGCCTAAGGCTG[A/G]TCTTAAATACCAACA | 68519 |
| rs253900065 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108477936 | ATAGAGATGCCTCGG[A/G]ATTGTGAAAGCTTAG | 68519 |
| rs253915526 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108420806 | CACCTAGTTTGCTCT[C/G]GCCCTGGGCATTCCA | 68519 |
| rs253923706 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108487978 | CTGACTCAATGCCAC[A/T]CATCTAGATGGGAGC | 68519 |
| rs253927282 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474874 | GAGGCAGAGGCCAGT[C/T]TGATCTTCAAAGGGA | 68519 |
| rs253929764 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457459 | TGTGTGAGTGTGTGA[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs253933189 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454253 | TCTTTCTTTTTTCTT[C/T]AAGTTTTACCTTGAC | 68519 |
| rs253933281 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108414150 | GCCTTTAGCCACCAT[-/G]GGCCTTTATCCCATA | 68519 |
| rs253934876 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108477550 | TCTTCTAATCTACAA[A/G]CATGGTCTTTCTATT | 68519 |
| rs253978356 | snp | A/G | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538442 | GTAAAGGAAGTCCCC[A/G]AGGTTTACATGGCAG | 68519 |
| rs254005315 | in-del | -/ATT | | | intron-variant | Eml1 | Mm_Celera | 12:108469996 | TCTTATCTTTTGTCC[-/ATT]ATTTTTTTTCCATTT | 68519 |
| rs254006788 | in-del | -/AAC | | | intron-variant | Eml1 | Mm_Celera | 12:108430574 | AAATAATTTGCTTTT[-/AAC]AACAACAACAACAAC | 68519 |
| rs254007970 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404967 | ACACACATGTGCACG[C/T]GTACAACACACAAAC | 68519 |
| rs254015131 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108498704 | GAATTTTGCCTGCAT[A/G]TACACCTGTGCACCA | 68519 |
| rs254047001 | in-del | -/GC | | | intron-variant | Eml1 | Mm_Celera | 12:108371893 | ATACCCTGATGTGTG[-/GC]TAGGATTAGCTACCT | 68519 |
| rs254057814 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108510882 | GACAAATAGGAGACG[A/T]CCAAGCTGGCATCCA | 68519 |
| rs254061324 | snp | A/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108413399 | GGGGTCTTGAGAGTG[A/T]CTCCTGCACATAACC | 68519 |
| rs254080296 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517368 | GTGGTATGTGTACAC[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs254090543 | in-del | -/TTA | | | intron-variant | Eml1 | Mm_Celera | 12:108527301 | TCTTGTGGTTGCAGT[-/TTA]TCTAGTAGCATCTCT | 68519 |
| rs254097166 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108510350 | TTGTAGTCACAGCAT[C/T]TGAGAACCATTGGGT | 68519 |
| rs254111758 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108461961 | GCAGAGCTGGAATTT[C/T]AACACCAATGGTTTG | 68519 |
| rs254132383 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449261 | CAGCTGACAGAGAGA[C/T]ACCTGTTGACGCCTT | 68519 |
| rs254147935 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108493482 | TCTGCATTTACACAG[-/C]CCAAGACAAGAGGTG | 68519 |
| rs254157603 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108498747 | GTTGGATCCTGGGAA[A/C]TGGAGTGAGTTAGAG | 68519 |
| rs254181750 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108389140 | TGGCCTTTCAGCCCA[C/T]TAAGCGTTTGTGTCT | 68519 |
| rs254183077 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517990 | ATAGAGAGTTCTAAG[A/G]CAGCCAGGGCTGTGT | 68519 |
| rs254191263 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108505361 | CTGAGCAGTGGTGGC[A/G]CACACCTTTAATCCC | 68519 |
| rs254194444 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468934 | GCTCAGATTTTAGTT[A/C]ATTCCAGATGTCAAG | 68519 |
| rs254216181 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453331 | GATAATCTCTTCTTC[A/G]GTAGGTCTTCATGTT | 68519 |
| rs254225522 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384801 | TGTCCTGGAAGTGTA[A/G]AGAAGTTCTTAGAGG | 68519 |
| rs254225784 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108517235 | CAGCAGGACATTATG[G/T]TTCTCCTGGTTACGT | 68519 |
| rs254230892 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108467524 | AGTCGGCACACGCAC[A/G]GCCTTCCTCTGCCTC | 68519 |
| rs254233312 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482575 | ATTATGGATGGTTGT[A/G]AGCCACCAGGTGGTT | 68519 |
| rs254280855 | in-del | -/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406843 | GGGACCAAGTGTTCA[-/C]CACTCATGACGTGTG | 68519 |
| rs254341070 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479434 | AAATTCCTTATTGAA[C/T]TCAGTTTGTTGGTAT | 68519 |
| rs254355741 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530522 | CAGCGAACCTTTTCG[C/T]CACTGTGCAGCTGTG | 68519 |
| rs254368967 | in-del | -/GTGTGTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108479064 | TTTGCAGGTATGAAC[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs254371059 | in-del | -/CGCG | | | intron-variant | Eml1 | Mm_Celera | 12:108462269 | ATGTATGAGTGCACA[-/CGCG]CACACACACACACAC | 68519 |
| rs254381901 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372018 | CAGTGTCTGTAGGTG[A/G]CAATGAGAACAGATG | 68519 |
| rs254406743 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446749 | TATGCTCCCAGACCC[C/T]GCAGAGCTGGGATCC | 68519 |
| rs254413325 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392091 | GTAGTCTCTGAAGTG[-/T]TTCTGAAACCGGGCA | 68519 |
| rs254415074 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108434193 | GAGGTTAAGTTCAGA[A/G]ACTAGGGTTTGAACC | 68519 |
| rs254415136 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108454601 | CTTCCTTCCTTCCTT[-/C]CTTTCTTTCTTCCTT | 68519 |
| rs254440425 | snp | C/T | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108370756 | GGCTCCAGATCCCGG[C/T]TACACCCCTAGAGGG | 68519 |
| rs254467065 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403643 | TATATCTAGAAACAG[A/G]ATTACTGGTCCATAT | 68519 |
| rs254473745 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405513 | GAACAGGCTAGCTCA[G/T]AGCATTAAAACAGGA | 68519 |
| rs254477693 | snp | A/C | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408646 | TGTAATGTTGACAGG[A/C]CCCATCTAACTACGT | 68519 |
| rs254505811 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108454635 | TCTTTCTATTCATTT[A/C]TTTATTTTGTGACAG | 68519 |
| rs254541682 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377445 | CGTGCGTGTGCCCTC[C/T]CTCGCCATGTGTAGG | 68519 |
| rs254544643 | in-del | -/GCCACA | | | intron-variant | Eml1 | Mm_Celera | 12:108397380 | CTTCCTTCCTTCACT[-/GCCACA]GCCACAGCCACATGT | 68519 |
| rs254548631 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471633 | TTTGTGCTTCTCATC[C/G]CTTGTGAGTTAATAT | 68519 |
| rs254563796 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402863 | CTCCTCCAGCATCCC[A/G]GGCAAAGCTCTCCAT | 68519 |
| rs254571715 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108451569 | GTTCAGATGTGCTCA[C/T]AGTAAGCCTGACACT | 68519 |
| rs254583277 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471076 | CAAAAGCATCGTTGC[A/G]TTAAGGAAGTGGCTC | 68519 |
| rs254595514 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108501229 | TGTTGATGGACACAT[A/G]GCTGATCCCATTCCT | 68519 |
| rs254636428 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108436897 | ATTTTCTGACACGAA[C/T]GCCTGATTGGGGCTT | 68519 |
| rs254653872 | snp | C/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108533257 | GACGCTTCCCAGTTC[C/G/T]CCACGTGCATTCTCT | 68519 |
| rs254670225 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108510781 | CTTGTGCTGATCACA[A/G]AGGCTCCTGGGAGCT | 68519 |
| rs254672247 | in-del | -/CTGAATGGA | | | intron-variant | Eml1 | Mm_Celera | 12:108438123 | TTTATCTTGTGAATC[-/CTGAATGGA]CTGTCTTTGTTGTGT | 68519 |
| rs254678275 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518230 | CTCTATGGACTTCCG[C/T]AGGCACTGTATACGT | 68519 |
| rs254683228 | in-del | -/GGAACTG | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538593 | ATGATAATGAAGTAC[-/GGAACTG]GGAACTGGGAACTGG | 68519 |
| rs254693919 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532842 | ACATAATTTGTTAGC[A/G]CTGACATGTACAGCA | 68519 |
| rs254701987 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442456 | GATTCACGGTCCACA[C/T]CACCACTCCTCAGCA | 68519 |
| rs254747174 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108503819 | ATTGTATGGGCGTTA[A/G]TCTTAGCACCCTGGC | 68519 |
| rs254765956 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108521599 | GTCCTTCGGGGGTGC[C/T]GTTGTGATGGTGGGA | 68519 |
| rs254775925 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108377986 | TGCTTCCACATGTGC[A/G]TACCTATGGTCAGGG | 68519 |
| rs254780960 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108525533 | TTAGGGTATAAAAGG[A/G]TATGAATATAAAAGT | 68519 |
| rs254799644 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108472389 | GTGGGATTCCAGACA[C/T]CTGTGTTATCGTTAG | 68519 |
| rs254821440 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405564 | CTTATTTTAAGTGAG[A/C]CTGCATGTTTGCTCT | 68519 |
| rs254830850 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108373073 | GCAGCGGAGGAGACT[A/C]TCTGTTCAGAAGTCT | 68519 |
| rs254830954 | in-del | -/CGCCG | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408711 | TGGCTGCCCTGGCCA[-/CGCCG]CGCCACCCCCAGAAG | 68519 |
| rs254868708 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475276 | AATAAAAGCCTCCTA[A/G]CATTAAATTTGCCAT | 68519 |
| rs254871311 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419710 | TGGCACTGGGCAGAT[A/G]TTTTTGGAGAATGTT | 68519 |
| rs254893642 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379237 | GCATAAGTGATATGC[G/T]TGTGTGTAGGTACAT | 68519 |
| rs254898534 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108478538 | AACTCAGGACCTTTG[A/G]ATGAGCAGTCAGTGC | 68519 |
| rs254900013 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108398432 | AGGACATGATAGGGA[G/T]GCTACAGGATGAGAA | 68519 |
| rs254933660 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429244 | TCTCTCCTTCCACTG[A/T]GTGGGTTCAGGGAAC | 68519 |
| rs254947096 | in-del | -/CA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108434629 | CACACTTAACACACG[-/CA]CACACACATCATTTA | 68519 |
| rs254953148 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410313 | TTCCTGACACATTTA[C/T]CATATGTGTCTCTCA | 68519 |
| rs254955036 | in-del | -/CTCT | | | intron-variant | Eml1 | Mm_Celera | 12:108433501 | TTGGATGGAGTTGGG[-/CTCT]CTCTCTCTCTCTCTC | 68519 |
| rs254966375 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108495397 | CAATCATGCTCTGAC[A/C]GAGGGGACAAGCCAG | 68519 |
| rs254972331 | in-del | -/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468380 | TACAAAATGAGTACA[-/C]CAAGAAGTCTGGTTT | 68519 |
| rs254986996 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525633 | AAAAATTTAAGAAAA[A/T]TTCTAAAAATAAAAC | 68519 |
| rs254993184 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108534327 | CTTCTGGCCACTTCA[-/G]CCACTGTATGTACAT | 68519 |
| rs254996917 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108459149 | CTCTACCTGGAACTC[C/T]AGGGATGCACCTAGT | 68519 |
| rs255008398 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108458213 | TCATTAGCTCCTGTG[C/T]ATCATGGCATCTGGC | 68519 |
| rs255046524 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108521497 | CGTTAATATGGACGC[A/G]TGTGAGTTTCCCAGT | 68519 |
| rs255055530 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108535600 | AGATGCCAGTGGGGG[-/C]GCAGAAAGGCAGTGT | 68519 |
| rs255066183 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445731 | AAGTGCATGAAAATT[A/T]TGTATGCAGAAAATG | 68519 |
| rs255066247 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108439869 | ATAATAAATAAATCT[A/T]AAAAAAAAAAAAGAA | 68519 |
| rs255079193 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108423631 | CAAACAAATCACTGC[G/T]GGAACAAAACCTTTG | 68519 |
| rs255092105 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108513883 | AAGCAACAGTCAGGG[-/A]TTAGATGCGACAGAC | 68519 |
| rs255123403 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432131 | TGTTAGGGTGTCAGG[A/G]CACTCAGGAAAACTT | 68519 |
| rs255189979 | in-del | -/GTGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108374344 | TGTTAGAGAGCATGT[-/GTGTG]GGGGGGGGACTCTGT | 68519 |
| rs255211100 | snp | C/T | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108400748 | TCTATATGAGAAGAC[C/T]TAGCAGTGTCACCTC | 68519 |
| rs255213288 | in-del | -/GCATATTAAAGCATC | | | intron-variant | Eml1 | Mm_Celera | 12:108443972 | CTCAGCATGGAACAT[-/GCATATTAAAGCATC]GCATCTTACTCTGTA | 68519 |
| rs255228288 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527795 | ACCTGCCGCTGCCCC[A/G]CAACAGCCTATGCCT | 68519 |
| rs255242416 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108409553 | CCCATCCCATACATA[C/T]ACTTCCTCTCTGTCT | 68519 |
| rs255243580 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108448934 | TCTCCACTTGTACCC[A/G]TGAACTGCTGGGACT | 68519 |
| rs255269922 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108393444 | AGGCAGAATAAGGCA[C/T]CAAGCCCCTCACCTC | 68519 |
| rs255276387 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429732 | TGGGGGAAAAAACCC[-/T]TAAATTGTGTTTTAA | 68519 |
| rs255283449 | snp | C/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108412088 | ATCCGACTGGGACCA[C/G]TCTCTAACTCCCAAG | 68519 |
| rs255283730 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108533524 | CTTGCCCTCGTCCCT[A/G]TTTTGCTAGGACATC | 68519 |
| rs255289636 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455258 | TTCTGGATCAGCACT[A/G]GGTGTCAGCGTGGTG | 68519 |
| rs255311602 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504688 | ACTCTGATCATTTTC[C/T]TTGCTCACATTATAG | 68519 |
| rs255318175 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108487536 | AGTGTGTGTGTGTGT[A/G]CGTGTACATATACAT | 68519 |
| rs255333813 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108498727 | GTGCACCATAAAGAA[-/AG]AGTGTTGGATCCTGG | 68519 |
| rs255335554 | snp | C/T | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108400938 | TGGGATTCCAGAGCC[C/T]AGCTCCTAGGGGGAC | 68519 |
| rs255350923 | in-del | -/TTCCTT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376291 | CTCCTCCTCCGCTTC[-/TTCCTT]CTCCTCCTCTTCTTC | 68519 |
| rs255354781 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486518 | TCATATGGGCTTTCC[C/G]TACACTCTTGTCCCC | 68519 |
| rs255354856 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108495114 | CTTTTTCTGGACACC[A/G]CACAGAATCACGGGA | 68519 |
| rs255356881 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508690 | ATCACCTGCCTCAAG[C/T]ACAGCCTGAGAGCAT | 68519 |
| rs255366962 | in-del | -/CA | | | intron-variant | Eml1 | Mm_Celera | 12:108475339 | GAGCTTTTTGTCTCT[-/CA]AAGTGGAATCTCTCT | 68519 |
| rs255386576 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108498658 | TGTTTCAACTTAAAA[A/T]TTTAAGTTAAATTTA | 68519 |
| rs255389630 | in-del | -/AC | | | intron-variant | Eml1 | Mm_Celera | 12:108485746 | CATTCACACACACAT[-/AC]ACACACACACACACA | 68519 |
| rs255395131 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108415529 | ATTCCTGTGCACAAA[-/G]CACACACAGATGCAC | 68519 |
| rs255428986 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108494546 | GTCATTGGCAGCAGT[A/G]TGAAGGCACTTTGTC | 68519 |
| rs255443304 | in-del | -/GA | | | intron-variant | Eml1 | Mm_Celera | 12:108444104 | TTCTTTTCTTTTCTT[-/GA]GATAGGGTTTTCCTA | 68519 |
| rs255456478 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108418877 | ATCCTCTTGCCTCCA[C/T]CTCCTTCACTGCTGG | 68519 |
| rs255472217 | in-del | -/GAGACAGC | | | intron-variant | Eml1 | Mm_Celera | 12:108489921 | GGCCAGGTGGCCACA[-/GAGACAGC]GAGTGTGCCCACCCC | 68519 |
| rs255474067 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380014 | TCCCTCCCCCTCTCT[C/G]TTTTCCTCTTTCCTC | 68519 |
| rs255474892 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108516832 | ATAGGCAGTCTTGTG[A/G]CCGGTTGGGTTTATC | 68519 |
| rs255514729 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430468 | GCAGTTCCTGACTGT[C/T]TGTAACTCCAATTCC | 68519 |
| rs255520097 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108458882 | TTGTGGCTTCAACAG[C/T]CCTTGCCAGGTCCAG | 68519 |
| rs255552544 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445181 | TGTGTGTGTGTCAGC[A/G]TTAGTTACCCCGCCT | 68519 |
| rs255557446 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108464579 | ATTTCAGCGGTCAGA[A/G]AGCAGAGGCAGGTGG | 68519 |
| rs255561904 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456863 | TCCTAATCTTTTAAG[A/C]CATAATAAATCTAAA | 68519 |
| rs255579211 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422568 | AGGAAGGGGAATGAG[A/G]TAATCTCTTTCTGCA | 68519 |
| rs255581880 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506459 | GAGGCATGTCACTGA[C/T]ACCTTCACTGTTTTT | 68519 |
| rs255589669 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108383858 | AATTCATGAAAGTTC[A/G]TCTTCATGTTGATCT | 68519 |
| rs255613990 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108434118 | CAGGGCTCCGGAGTG[A/G]CTACTCTGTGTCCAT | 68519 |
| rs255632091 | in-del | -/CACACA | | | intron-variant | Eml1 | Mm_Celera | 12:108485339 | TATGTTCTTTGAAGC[-/CACACA]CACACACACACACAC | 68519 |
| rs255642659 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108463911 | AAGGGACCATGCACA[C/T]GGACCACTGAGGACA | 68519 |
| rs255647958 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479318 | GCTGTGTAATGTTTG[C/T]TCTTCATCTCTTAAT | 68519 |
| rs255664880 | in-del | -/AA | | | intron-variant | Eml1 | Mm_Celera | 12:108373717 | TCATCTGGAGCCTGT[-/AA]AAAAAAAATGTGGTA | 68519 |
| rs255669018 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108389441 | TGTGCACTCAGGAAC[A/G]CCTTATAACTACTAT | 68519 |
| rs255675794 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108375695 | CATCTCTGGAGGAGA[C/T]GCCCAAATACTCTGC | 68519 |
| rs255686768 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108440838 | GCCAGCGCAGAGCCA[G/T]TCTTCTTTTCCTCGT | 68519 |
| rs255695222 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108385896 | CTCACACCTCCCCCT[A/C]CCCCCAGCCTCTGGC | 68519 |
| rs255704877 | snp | C/T | | | utr-variant-5-prime, intron-variant | Eml1 | GRCm38.p3 | 12:108422875 | CTACCCCCACCCCCA[C/T]CCCGTAGCATTCTGC | 68519 |
| rs255717522 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526826 | ACAGCCCAAGACTGG[C/T]TCCGGTGCTCCTGTC | 68519 |
| rs255755131 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108485369 | CACACAGAGGCACCC[-/AT]ACACACACACACACA | 68519 |
| rs255792640 | snp | G/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536552 | GGGACTCGAACCTTG[G/T]TCCCACCACTTTCAG | 68519 |
| rs255805690 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108476600 | ATTTGTCCAGTGGGT[C/T]AATCTTGACATCTTT | 68519 |
| rs255815358 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108391981 | GAGTCTGAGTGCCCC[C/T]TGCCCCTTAACTACC | 68519 |
| rs255822347 | in-del | -/GTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108425716 | GGGAATCTCAAACAC[-/GTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs255824252 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108528166 | CATAGCCAAATTACA[G/T]TTATGAAGTAGCAGT | 68519 |
| rs255834267 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108513753 | CTGGCCTGACATTCT[A/G]TCTTCTAACATTGCC | 68519 |
| rs255844947 | in-del | -/TC | | | intron-variant | Eml1 | Mm_Celera | 12:108475349 | TCTCTCAAAGTGGAA[-/TC]TCTCTGTCATTAAAT | 68519 |
| rs255850676 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108497265 | GGTGAGAAACGCCTC[A/C]GCAAGCTCATCTGAA | 68519 |
| rs255869382 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108424726 | TCTTCAGGGGAGGAC[A/G]CCCAGGTTCTTTGGT | 68519 |
| rs255882638 | in-del | -/TGG | | | intron-variant | Eml1 | Mm_Celera | 12:108520614 | GTGGTTGGGTTTTTT[-/TGG]TTGGTTGGTTGGTTG | 68519 |
| rs255883531 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108481739 | CCCTCTCCTCCCAGG[A/G]CCCCCTCACGCAGAC | 68519 |
| rs255922748 | in-del | -/T | | | utr-variant-5-prime, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410646 | CAGATACACAAGGTC[-/T]TGTGGCAGAAAGCAG | 68519 |
| rs255933965 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496648 | AGTTGAGGAAATGCC[C/G]CCACCAGATTCTGTG | 68519 |
| rs255975095 | in-del | -/TTTC | | | intron-variant | Eml1 | Mm_Celera | 12:108379642 | ATGAAGCTATTTGAG[-/TTTC]TTTCTTTCTTTGATC | 68519 |
| rs255979217 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108429716 | AAGCCAAGTGCTTGG[A/G]GTGGGGGAAAAAACC | 68519 |
| rs255983554 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460280 | GTTAGAGTATCACCG[G/T]GGTGTATTTTAGATT | 68519 |
| rs256005798 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447741 | ACCTTGCCCGCTTAC[A/G]TGAGGGAATGACCAA | 68519 |
| rs256007007 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108467870 | CTAGGACAGTGTCAA[C/G]CAAATGCTGACTTTG | 68519 |
| rs256017841 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108373774 | CGTCAAGAGGGGAGC[A/T]CAGCGGGCGGCGCAG | 68519 |
| rs256043560 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447294 | CCATCTTTGTTAAAA[C/T]GAGGATGAGTGGATA | 68519 |
| rs256051675 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108519156 | AGACATCACACATGC[C/G]GAGTTCAACTCTGTA | 68519 |
| rs256058319 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437723 | TATCTCATGAATGTT[A/G]GATTCCGGTGCCTCA | 68519 |
| rs256096073 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108480338 | TCCTTTCTTTCTTTC[C/T]TTCCTTCCTTCCTCC | 68519 |
| rs256144935 | in-del | -/TA | | | intron-variant | Eml1 | Mm_Celera | 12:108453517 | CTGCCCTCTGGGTTT[-/TA]TGTGTGTGCTGCGAT | 68519 |
| rs256161167 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108441510 | GAGACGAAGCCATTG[A/C]TGACTTTATAGGCCC | 68519 |
| rs256163317 | in-del | -/ACACATACC | | | intron-variant | Eml1 | Mm_Celera | 12:108434846 | TACATATACATACAT[-/ACACATACC]ACACATACATGCAAA | 68519 |
| rs256189554 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108487140 | TGCCATCGTGCCTAC[A/G]ATATTGGGTACTATG | 68519 |
| rs256218489 | snp | C/T | | | intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108537766 | TGCCTACCTACTCCC[C/T]ATCTCCCCACGCTCA | 68519 |
| rs256226477 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108513566 | ACTTCTCGTTTCTCC[C/T]CTTGGCATCTGTCGG | 68519 |
| rs256252502 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108392216 | CACCAGCTTGGCAGA[A/G]CCCCTGTCCCTCCAC | 68519 |
| rs256287663 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422160 | TAATGAAGTGTGAGA[A/G]ACCCCAGAGCCCCGG | 68519 |
| rs256288502 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442371 | AGCACCCACCAACCC[C/T]GTCTGAGACAACTCA | 68519 |
| rs256308123 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470312 | AATTTGTGTTTCTGT[C/T]CTCTTTAAATTTCTT | 68519 |
| rs256341917 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108411935 | GGGAGGGGGAGTTGG[-/TT]GTTTTTTTTTTTTTT | 68519 |
| rs256342636 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108387885 | AGATCTCACCCCCCT[C/G]CGAAGGCAAGGATCT | 68519 |
| rs256349171 | in-del | -/CAGCACAT | | | intron-variant | Eml1 | Mm_Celera | 12:108487881 | TCTCTGGCCTCTACC[-/CAGCACAT]CAGTAGCAACCCCCC | 68519 |
| rs256350060 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108519531 | CGCATCTCACCAAGG[C/T]ATGGAGCTTGCTTAT | 68519 |
| rs256353542 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108388132 | AAGGCCGGGTCTGAA[A/G]TTAGTGTCCCAGGGC | 68519 |
| rs256370605 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108439298 | CACTCTGTAGACCAG[C/G]CTGGCCTCCAACTCC | 68519 |
| rs256382028 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518993 | TTGTTTTTTTCTGTA[C/T]GTGCTTTCTTTTCCC | 68519 |
| rs256382283 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108386446 | CCGGATGCTTGCCAG[A/T]GGACATCATTGCTTG | 68519 |
| rs256394798 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108481986 | AGACAAGATGGCCCC[G/T]GCTCCTCACCACAAA | 68519 |
| rs256403918 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484683 | TCCCTCAGGAGCTTC[C/T]AAGTCTGCGCTGGGT | 68519 |
| rs256411446 | in-del | -/GCCAA | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408712 | GGCTGCCCTGGCCAC[-/GCCAA]GCCACCCCCAGAAGA | 68519 |
| rs256412138 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108497407 | TCAATCAGGTCCTCC[A/T]GCAGGAGATACTTCT | 68519 |
| rs256425443 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504841 | ATACCGAAGTATTTT[A/T]GGGTCCTAGAGAGAT | 68519 |
| rs256425856 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532752 | AAATAAAAAATGTAA[C/T]TTTATTTTGAGTCTT | 68519 |
| rs256443954 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108535091 | TGGCCTTACAGCCTC[G/T]TGGAGTCTTCCTGAC | 68519 |
| rs256455806 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108444340 | GACAAAGATGGCTGT[C/T]GTGTCCCTCAACAGA | 68519 |
| rs256465218 | in-del | -/GAG | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412741 | TAGATCTCTGAGTTC[-/GAG]GTCAGCCTGATCTAC | 68519 |
| rs256565975 | in-del | -/AAA | | | intron-variant | Eml1 | Mm_Celera | 12:108531510 | CAAGACCCCGTCTTT[-/AAA]AAAAAAAAAAAAAAA | 68519 |
| rs256592160 | in-del | -/CCCTCA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468898 | GAAGAAGAAGAAGAT[-/CCCTCA]CGGGTGTACCCTGCT | 68519 |
| rs256605841 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108417934 | TAGTCATCTGTCCCT[C/T]AGCCTCCAAAGTGCT | 68519 |
| rs256633254 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108453962 | AGGATGTGTGGTTAA[A/G]TGGCTGGATCGCTCC | 68519 |
| rs256634139 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408281 | AATTTATTATTTCAT[A/G]CATACATGTACAATC | 68519 |
| rs256647115 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480622 | CAGAGGACTACACTT[C/T]CCTCAGTGGGCTTCT | 68519 |
| rs256656622 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108503617 | ACGTAGGCTGTCCCC[A/G]TTTATAGTACACGAT | 68519 |
| rs256664605 | snp | A/G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379685 | ATTATTTATTTTTTT[A/G/T]TTTTGTGACAGGGTC | 68519 |
| rs256673864 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108427611 | GAGCCAAAAGTTGGC[C/T]CCCATTTTGTTCTCT | 68519 |
| rs256674598 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460279 | TGTTAGAGTATCACC[A/G]GGGTGTATTTTAGAT | 68519 |
| rs256694811 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108510256 | GGAAAGGTGAGGTTT[C/G]CTCCTTGTCTTTCTG | 68519 |
| rs256717172 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474393 | CAGACAGATGAGAGA[A/G]GAAGGTGCCTGTGGG | 68519 |
| rs256717277 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482338 | ATGGAGGAAGACTCC[C/T]GATGTCCTCTGGCCT | 68519 |
| rs256722093 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524086 | TCTCAGCACCTCATT[C/G]GAGCTTCTCCAAAAT | 68519 |
| rs256731815 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108426399 | AGAACAGGCTCTCTC[C/T]TTCCACCATGTGGAC | 68519 |
| rs256738114 | in-del | -/TTTA | | | intron-variant | Eml1 | Mm_Celera | 12:108443701 | CTACCGGGATGGCTG[-/TTTA]TCTCTTGCACACCCA | 68519 |
| rs256755716 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522074 | AGTGCTCTGAGCAGA[C/T]CTTGGGTGCAACTCT | 68519 |
| rs256760574 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108530227 | TTTAAATGCCCCGTG[A/G]CAAACAGACTTCTGC | 68519 |
| rs256811064 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108466400 | CACCTCAGTATTTGG[G/T]GTGCTTCCTTTATCT | 68519 |
| rs256831120 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108373039 | ACAACAAAACCAAAC[G/T]AGACTAAGGCTGCAG | 68519 |
| rs256840951 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108438822 | AACCCCATGAGGCTC[A/G]TGGGCCCTGTAATCT | 68519 |
| rs256841138 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108484476 | CCCATCATCCACATA[A/C]TGTCACCTCTCCCAG | 68519 |
| rs256867531 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410158 | GTCCAGAGACTCCAA[C/T]ACAGGCTCTTCAGGC | 68519 |
| rs256886222 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507911 | ATTTTGGCTCATGCC[A/G]TGGTAGGGGATCTGC | 68519 |
| rs256893236 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474290 | GGCCAGCCTGGTCTA[C/T]GAAGTGAGTTCCAGG | 68519 |
| rs256914769 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108377773 | TATGTATGTGTGGTG[A/C]TCAGGAGACAGCTTG | 68519 |
| rs256926541 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507347 | TTTAATCCCAGCACT[C/T]GGGAGGCAGAGGCAG | 68519 |
| rs256926837 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492403 | TTTCTCCTTAGCCTC[C/T]AGTTCAAGATCTCCT | 68519 |
| rs256929323 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473713 | TTCTAACCAAGGTAA[C/T]GGCTCTCTGGGACAG | 68519 |
| rs256929995 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108441498 | AGGGGCTTCACGGAG[A/G]CGAAGCCATTGATGA | 68519 |
| rs256939796 | in-del | -/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108463256 | CTCTAGGTTCCCTAG[-/T]ACCACTGAGCAAGCA | 68519 |
| rs256944886 | in-del | -/C | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411389 | GCTGTTCTACTGAGA[-/C]CCCCACAGGACCCAC | 68519 |
| rs256950365 | in-del | -/AGA | | | intron-variant | Eml1 | Mm_Celera | 12:108478013 | AATACAGCTGAACAG[-/AGA]GTGGGTATCACCTAC | 68519 |
| rs256950610 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108487021 | TAACCCAGAATCAAG[A/T]GCTTAATGAATCAGT | 68519 |
| rs256988819 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108398030 | GATGCTCATTGAAGA[G/T]CTTTTCCAACTGCTA | 68519 |
| rs257023116 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108385616 | GTTTGGCCATTTGCT[G/T]CTGGGGATGTGGTTT | 68519 |
| rs257028565 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446813 | CAAGGCATGGCATCC[C/T]ATTCCAAGTATGCCA | 68519 |
| rs257034474 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108441778 | AAGGGTTTGCTTTGG[G/T]TTTGCCTTGTCTGTG | 68519 |
| rs257036673 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408071 | GCAAAGCCTCAAAAC[C/T]GAGAGGTTCACTACG | 68519 |
| rs257037772 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108387032 | GGGGAGGAGAGCGGA[C/G]TCTCTGAGGAGCCCT | 68519 |
| rs257057285 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376850 | ACTGCCTCCTGGGAG[A/T]TGTCGGGTGTGGAGA | 68519 |
| rs257057337 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108382205 | GCAAGAGAAGGGCCA[G/T]TTTAAAGTACAGTTT | 68519 |
| rs257059586 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455767 | TTGATCAAGAAACCA[C/T]ACAACCCCACCCTGA | 68519 |
| rs257084213 | in-del | -/TGCCTG | | | intron-variant | Eml1 | Mm_Celera | 12:108458989 | TGCCTGCCTGCCTGC[-/TGCCTG]CTGCCATGCTCTCCA | 68519 |
| rs257093937 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108441273 | GAATCCAGCTCATGG[C/T]CCTAAACTCACGCCG | 68519 |
| rs257102173 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108447136 | TCAGCTGTCCTGACT[A/G]CTCCCGTGCCAAATG | 68519 |
| rs257126572 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108416187 | AGGGAAAGTTGGATT[A/C]TGGAAAATACAATGA | 68519 |
| rs257129278 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478153 | GTGAACATTTCCTTC[A/T]CGCACTGTCACCATC | 68519 |
| rs257140906 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446650 | GGCTCAGTTGTTCCA[A/T]CTTCTTTATAAAGCA | 68519 |
| rs257169827 | snp | G/T | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411439 | AACATATCATGGCCA[G/T]CATACCAGGGGACTC | 68519 |
| rs257170537 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108415022 | TAGCTGGAATGACTA[C/T]ACAATCTATTATCCT | 68519 |
| rs257171247 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108485069 | GTCAAAAGCCAGCAC[A/G]TTAGGCGGCCTTTAC | 68519 |
| rs257173301 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477794 | AGTTTTGCTGAACTT[A/G]TTTACTTGTTGTGCC | 68519 |
| rs257185768 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388829 | CTTCCTGCATTATCC[A/T]CTGAAGCAGGCTATA | 68519 |
| rs257186118 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470410 | GATATTTATTAGATT[A/T]ATTTTAAAAATTTTA | 68519 |
| rs257201064 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108375882 | AGCAGAGGGGTGGGG[A/G]TGGGGGAGGGGATAG | 68519 |
| rs257215758 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458774 | GTTTCATAGTTTCAC[A/T]TATTGGAATATTTGA | 68519 |
| rs257218880 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523130 | AAAGAAAGAATATTA[A/C/T]AAGCAGTAAGGGATA | 68519 |
| rs257249997 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108508251 | ACTAATCCTCTGACT[C/T]CACTTGTACACAGGC | 68519 |
| rs257266130 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477670 | TAAGATAATGTTGTC[A/G]CTAAGTAAGCATTTC | 68519 |
| rs257269560 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469337 | CAGGGTCCCAGCCCG[A/G]GGATGGTTCCACCCA | 68519 |
| rs257290253 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108489080 | ACATGTTGGGTCGGT[G/T]AGGTTCCCGTGCTTT | 68519 |
| rs257301676 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108435448 | CACTGCACACCATGG[A/G]GACCGGATGTAAGTC | 68519 |
| rs257302042 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108428645 | TTCCCTTTGAAGGAG[A/G]TGTTGAGAAAAATCT | 68519 |
| rs257302292 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476769 | ACCTTCATCTTTGTT[A/C]CCTCCCTCAGCCCTG | 68519 |
| rs257335055 | in-del | -/CACACACACACACACACACA | | | intron-variant | Eml1 | Mm_Celera | 12:108414395 | GCGCATTCACTCGCG[-/CACACACACACACACACACA]CACACACACACACAC | 68519 |
| rs257353796 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473807 | TATCACCTCCCAGCT[C/T]GGTTTCCTGCTGCTG | 68519 |
| rs257362236 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108452917 | TTGATGATTTTACTT[-/TG]TGTGTGTGTGTGTGT | 68519 |
| rs257378256 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108463336 | ACGTGGCAAGCCCAT[A/G]GAGCGTGCGTGATGC | 68519 |
| rs257399879 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496758 | CTGGTGATCCTGGGT[A/G]CTTTAAGAAAGCAGA | 68519 |
| rs257401430 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108515092 | GTAAATAACATTCCC[A/G]CACTTACTCATTACA | 68519 |
| rs257412913 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433538 | GCTATATAGGGTTTA[C/T]AAGGTGTTTTAGCCC | 68519 |
| rs257418011 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475547 | CAAAGCTCACTTCTC[A/G]CCCTCCGTCGTGTGG | 68519 |
| rs257431103 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108499228 | TCACTCACACACCCC[A/C]ACCCACACACACACA | 68519 |
| rs257456623 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108531994 | agggaaaggaacaga[A/G]aaagggagagaggga | 68519 |
| rs257458912 | in-del | -/CCC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473315 | TACACCAAGCATACA[-/CCC]CCCCCCAAGCACACA | 68519 |
| rs257464504 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433929 | TAGGAACCATGTTCT[C/T]TTTATCCAGCAGAGA | 68519 |
| rs257495725 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108474960 | CCAAACCAAACCAAA[-/T]CCAAACCAAACCAAA | 68519 |
| rs257521444 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108449057 | CATCTGCAGTTCTTG[C/T]TTTTGCTCCTTGAGT | 68519 |
| rs257526846 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530463 | GTTGACAAAGCTCCA[C/T]CAAGGGACTTAACTT | 68519 |
| rs257533196 | snp | A/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108537027 | CAGTGGAAAGACATC[A/G]GTTTATAAGCAGGGC | 68519 |
| rs257556105 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108396473 | GCTACACTGATGGCC[A/G]ATGGATACCAGTGGC | 68519 |
| rs257588000 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108489501 | GGAAGAGGAAGAAGA[A/G]GAGGAAGAGGAGGAA | 68519 |
| rs257593245 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108379442 | CGTCTCTCTGGTCTC[-/TT]TTCTCATTGATCCCA | 68519 |
| rs257622591 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108420048 | TTAAGAGATTTTCTT[C/T]CCTTGAACATCTTAG | 68519 |
| rs257623893 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108414044 | CACGCTTCTCACCGG[A/C]TTGGCCAACACACAG | 68519 |
| rs257624167 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403159 | ACCACCCGTCCCCTC[C/T]AACACCCAGGCTCTA | 68519 |
| rs257627471 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451264 | TTTAACATTGTGTCC[C/T]GCAGACACACACAAT | 68519 |
| rs257645965 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466037 | GATTTCCCTGCTATG[A/G]CCGGCGATACCTGGA | 68519 |
| rs257646437 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108395425 | CACAGTCACTGTCAC[C/T]TCAGTGCTGGAGTGG | 68519 |
| rs257681715 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421327 | CCAACCTCCTGGAAG[C/T]TCTGTGCTGGCGGCT | 68519 |
| rs257688452 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402747 | GCTCAGGCCTAAGCT[C/T]CCGCTCTGTTCTCAG | 68519 |
| rs257707517 | in-del | -/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421229 | AGGTCCCCTGGAGGC[-/T]CTCTGCCACCATCAT | 68519 |
| rs257713565 | in-del | -/AGAG | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407473 | TAGAGAGACAGAGAT[-/AGAG]AGAGTCAAATAAGAT | 68519 |
| rs257723083 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108517714 | TTGTGTAGCACAGGC[C/T]AGCCTCAAACTCACA | 68519 |
| rs257734119 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108467133 | CCAAGGACCTTTTCC[A/G]GGGCCCACAAAATAC | 68519 |
| rs257736248 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108500917 | AGGCTCTAGGCAGTG[A/G]GGGTCTCCCGGTGTC | 68519 |
| rs257758635 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108442213 | AAGGTTTCTGAATGC[-/A]AAACCACCAAAAATG | 68519 |
| rs257762755 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108518733 | TAAGACAGAGTTTCT[G/T]TGTAGCCCTGGCTGC | 68519 |
| rs257767878 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402148 | CTCCCGAGTGCTGGG[A/G]TTGAAGGCGTGCCCC | 68519 |
| rs257778470 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525716 | CAGCACTCGGGAGGC[A/T]GAGGCAGGCAGATTT | 68519 |
| rs257815807 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108501076 | ACAGTTGAGTAGGAC[A/G]GTGGGCGGTCTCCAG | 68519 |
| rs257841601 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108500422 | CGTCTATTTTCTGTT[C/T]CTTTATTTATAATGG | 68519 |
| rs257849608 | in-del | -/ACC | | | intron-variant | Eml1 | Mm_Celera | 12:108434852 | TACATACATACACAT[-/ACC]ACACATACATGCAAA | 68519 |
| rs257858866 | in-del | -/CAGAGAA | | | intron-variant | Eml1 | Mm_Celera | 12:108445949 | GGTTAAGAACACGTT[-/CAGAGAA]CCCAGGTTCGATTCC | 68519 |
| rs257872083 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437138 | TTGAGATGGCGAACT[A/G]GCTTATTTTTCCTGA | 68519 |
| rs257956622 | in-del | -/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474513 | TTTAGAAGAAAAAAA[-/C]AAAAACAAAAACAAA | 68519 |
| rs257959902 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108416755 | TGATTGACCATGGGC[C/T]TACATTCACCCCTTG | 68519 |
| rs257963338 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108513384 | CTTGAGGCATGCTCA[A/G]GACCAGCCACTCTGT | 68519 |
| rs257999713 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520017 | CCATTCCTTCCAGCT[C/T]AGCTTCCTAAGCACT | 68519 |
| rs258000267 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376808 | AAGATACAGCTGACA[C/T]GAAGGGATTGACCTG | 68519 |
| rs258018934 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532299 | GAGAGCATCAGATCC[C/T]TTTACAGATGGGTGT | 68519 |
| rs258035460 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108425050 | CAAAGAGACTTTGGG[C/G]GATAGACATGGCTGT | 68519 |
| rs258041755 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108399224 | TTCTCCTACAGCATT[A/G]GTGTGACAGAAGCTT | 68519 |
| rs258045816 | snp | A/C | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108405943 | TCCTTGATCTGAAAC[A/C]ACCCCACCCCAGGCA | 68519 |
| rs258069002 | in-del | -/AGAT | | | intron-variant | Eml1 | Mm_Celera | 12:108460385 | ACGAGTTCAGATAGG[-/AGAT]GGATGTCCCGCCCTT | 68519 |
| rs258083173 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108470523 | GATCCTTTGTAACTG[A/G]AGTTGTGGACAGTTG | 68519 |
| rs258102207 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108386365 | CAAGCCTCAGTTTGC[C/T]TGCCTGTATAAGGGG | 68519 |
| rs258102735 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108398806 | ACTCTGACTCATGTG[C/G]GACAGAGAGGACTTT | 68519 |
| rs258112040 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405235 | TCCGTTCTTGTATTA[G/T]CGGTGAGGCATTGTG | 68519 |
| rs258114048 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108414130 | TATGGGGCCCTGGAT[C/G]GAGAGCCTTTAGCCA | 68519 |
| rs258118229 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108437555 | ACCAGGACTGTATGC[A/G]GCACGCTCAGGGCGC | 68519 |
| rs258137606 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108477734 | TTCCTTTCGGATCGG[A/G]AGGGAATACACCCGA | 68519 |
| rs258147231 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108484653 | CTCCCACTGCCACAG[A/G]GCCCTTTCAGCAGCT | 68519 |
| rs258153610 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108503702 | AAGGAAGCGTCAGGC[A/C]CACGCATTCTTCACT | 68519 |
| rs258158681 | snp | A/C | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404797 | ATACACACGCACATG[A/C]ACACACACACGTGCA | 68519 |
| rs258169367 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482721 | TAGTGATGGAGAAGA[A/G]TGTGTTTTATTTAAT | 68519 |
| rs258177169 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442943 | TGTCCAGGAGCATCA[C/G]ACTGTCAGCTAAAAG | 68519 |
| rs258203925 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108490703 | CCTCCTGAGTTCCTG[G/T]GTAGCCAGTGAGACA | 68519 |
| rs258237110 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108510379 | GTCCTCACCAGGGGC[C/T]CTCACTGCAAACTGA | 68519 |
| rs258238416 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503110 | TTGTCCCCTTGGGGG[C/T]CAGGGTAGCACCGGT | 68519 |
| rs258262534 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108372938 | TACACAGAGAGATTG[C/T]GTCTCAAAAACCAGA | 68519 |
| rs258274188 | in-del | -/TGAGTGTCCCTGTGTCAGGG | | | intron-variant | Eml1 | Mm_Celera | 12:108417689 | AGTTTTGGGAGGGGC[-/TGAGTGTCCCTGTGTCAGGG]ATGCTGTGGAACAGA | 68519 |
| rs258275655 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108509713 | CCAGACTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 68519 |
| rs258282910 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108472904 | TACACAAAAGCATAC[C/T]CATCAAACACACATG | 68519 |
| rs258284707 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108418021 | GGAGTGGAGTCTGCA[A/G]ACTAACCAGTCCTTG | 68519 |
| rs258317744 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108456912 | TGGTGGATTCTCCAT[A/G]TAAGTCGGGAGACAC | 68519 |
| rs258322245 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379083 | GGACTAGCTCATATT[C/T]CCACCAGCCATGGAT | 68519 |
| rs258322282 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372120 | TCATGAGTGCAGCGG[C/T]TCCTCTGAGACAGGA | 68519 |
| rs258327631 | in-del | -/ACCAC | | | intron-variant | Eml1 | Mm_Celera | 12:108472845 | CCACACCTCACATAT[-/ACCAC]ACCATACCACACCAC | 68519 |
| rs258343625 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464333 | GTAACTTTGTAGTGA[C/T]GGAGCCTTCACATTT | 68519 |
| rs258345895 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524967 | CACTGTGCTTGAAAT[C/T]AGAATTTTCTTAATG | 68519 |
| rs258355713 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455980 | ATTTCTGGTGGACAC[C/G]GTCATGAGCTCATGT | 68519 |
| rs258356503 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108508672 | AGCCTGAGCTACCCC[A/G]TGATCACCTGCCTCA | 68519 |
| rs258358584 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108516258 | TGACACTATACTTTT[C/T]TCAGTCATAGGACGA | 68519 |
| rs258388929 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471741 | CCTGCCACTTTGCTG[A/G]CTTTTAGAATTGAAT | 68519 |
| rs258396440 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455473 | TATTCTTTGTAAAAC[C/T]ACCATTAAGGAGACT | 68519 |
| rs258424882 | in-del | -/CTA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474439 | CAACCTTTTGGGACT[-/CTA]CTTTCATCAGGGCCA | 68519 |
| rs258432372 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108455066 | ACCGTGTGTGCATGT[A/G]TGTGCATGTGTGTGT | 68519 |
| rs258437818 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108389600 | ATATGAGGTATGGGG[C/T]GCCTGGAACCCAATG | 68519 |
| rs258441374 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471543 | GGAGGAGGAGGAGCT[A/G]GGGAGGAGGAGCTGG | 68519 |
| rs258443365 | in-del | -/TAACACCACCAGTGTGAGG/TAACTCCACCAGCGTGAGG/TAACTCCACCAGTGTGAGG | | | intron-variant | Eml1 | Mm_Celera | 12:108371789 | ACTGGGATGTTCTGA[lengthTooLong]TCAGCTCCTGAGGAT | 68519 |
| rs258453550 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440920 | GTCACTTCACTGCCA[C/T]GTTGAGGCTTAGGAA | 68519 |
| rs258469967 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524154 | ATCCCAGCACTCAGG[A/T]GGCAGAGGCAGGCGG | 68519 |
| rs258486933 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108414246 | AAAGGCCCAGAGCCC[C/T]GTCATCTCCACAGTT | 68519 |
| rs258495967 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496209 | AGAAACAGCTTGCCT[-/G]GGGCTGTATAGCCTC | 68519 |
| rs258498500 | in-del | -/GGGGT | | | intron-variant | Eml1 | Mm_Celera | 12:108397233 | CATTCTATTGGGTTG[-/GGGGT]GGAGGGGGCATTCCG | 68519 |
| rs258509600 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108446161 | ATTTATTTAGATAAA[A/G]TCTCATTGTGTAGTT | 68519 |
| rs258516285 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461986 | GGTTTGACTCCACAG[C/T]GTGTGCTGATTGTAA | 68519 |
| rs258523162 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530212 | TAAGAGCTGAGTGGG[-/T]TTAAATGCCCCGTGG | 68519 |
| rs258531581 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108431858 | TATCTACTCCTCCAG[A/C]CTCCGCCCTCAGCCC | 68519 |
| rs258548512 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421572 | CTCATCCTTCTGGGC[C/T]TGTCTTACAGTGATC | 68519 |
| rs258549923 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417675 | ACTGGGATTCTTCAG[-/T]TTTTGGGAGGGGCTG | 68519 |
| rs258567145 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108494114 | ACAGACTTTACCTCA[C/T]CCTACAAGGCTCAGC | 68519 |
| rs258574071 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388853 | GGCTATACCATAAGA[A/T]CACAGGGCTTGCCCA | 68519 |
| rs258607725 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108395334 | CCTCTCCTCCGCCCC[A/G]GGAGCAGGAAGGAAA | 68519 |
| rs258634618 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108445119 | GGGTTAATTAAGGGA[A/C]TAACATAAACATTTG | 68519 |
| rs258638960 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108434781 | TACATAACACATACC[A/T]CATATCATACACACT | 68519 |
| rs258642545 | in-del | -/TTGGTTA | | | intron-variant | Eml1 | Mm_Celera | 12:108454370 | ACGGACACTTGACAT[-/TTGGTTA]CCTGAACAACAGTAG | 68519 |
| rs258659590 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108526745 | ACAACTCACACACCC[C/T]ACCTAAGGAAACAGC | 68519 |
| rs258665453 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108430205 | CTGACAAGCACATTT[A/C]CTATCCTGCTGGGAG | 68519 |
| rs258665665 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108395458 | GAGGGGGAGTGGATG[A/C]AGGCAGATGCCTGGC | 68519 |
| rs258683504 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108391306 | GCCCCTCAGTGATAA[C/T]TGTCATCCTGACAGA | 68519 |
| rs258690805 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108445363 | ACAAAGCAAAACAAA[A/G]CAAAACTTTTCCATA | 68519 |
| rs258698236 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532849 | TTGTTAGCACTGACA[C/T]GTACAGCATTTGATT | 68519 |
| rs258708812 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108493329 | TGTTCCCAGCATCCA[C/T]GTCGTGGGAGTTGGG | 68519 |
| rs258709260 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442107 | CTGCCACACAGGGTC[C/T]GCCAGAACCGGACTC | 68519 |
| rs258747353 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108459871 | ACAGCAGTAAGGAAG[A/G]GGAGCTATAAGGTTG | 68519 |
| rs258760315 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108488225 | CTGAGCATATGCCCC[A/G]TGTGCCCTCAGTACA | 68519 |
| rs258775506 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108451438 | GACCCCAGCATAGGT[A/G]ATGGATGATCTGTAG | 68519 |
| rs258784974 | snp | C/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538923 | CACCTCGATTCACGG[C/T]GAGACATTTAGCCAC | 68519 |
| rs258788627 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447548 | TCATCACTTCGGGGA[A/G]CCTGGCATTGTGTGG | 68519 |
| rs258795617 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108496238 | TCAAAGGAACCCTAG[A/C]ATTTAGATCGGAAGG | 68519 |
| rs258798637 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108459227 | ATCTGGGTCCTGGGG[A/C]TCCAAACTGAGGTCC | 68519 |
| rs258807298 | in-del | -/AT | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404782 | TGCACGTGCAAATAC[-/AT]ACACACGCACATGAA | 68519 |
| rs258833800 | in-del | -/CA | | | intron-variant | Eml1 | Mm_Celera | 12:108485599 | ACACACACATACATG[-/CA]CACACACACACACAG | 68519 |
| rs258843841 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108415314 | TACGTTATTGTATGT[-/G]GGATATTTAGATGTT | 68519 |
| rs258844827 | in-del | -/ACAA | | | intron-variant | Eml1 | Mm_Celera | 12:108502525 | GCCACTGGTACTCAG[-/ACAA]CAAACAGTCAGTCAT | 68519 |
| rs258863704 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421163 | CCCCCAGTCTTTACC[C/T]GCAGCATCCAGGAAT | 68519 |
| rs258878682 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467013 | ACCAAACTCAGGTCC[C/T]GTGAAAGATTCGTGC | 68519 |
| rs258884636 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108524452 | GGTCAAGGAAGAAAT[-/A]AAAAAAACTAATGGC | 68519 |
| rs258905122 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108426199 | TGGGGTACAGGTATG[C/T]GTCATTGCACCTGAC | 68519 |
| rs258936343 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108430327 | TATTTGTTTTTTTTT[C/T]CCTAAGAGCATAGCA | 68519 |
| rs258937119 | in-del | -/TTAC | | | intron-variant | Eml1 | Mm_Celera | 12:108426494 | AACCATTATTTTATT[-/TTAC]TTATTTATTTATTTA | 68519 |
| rs258959875 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433128 | GTACACATTTAGTAA[C/T]CCTCCCTCCCTGGGG | 68519 |
| rs258963770 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108464229 | CACAGCCTTCAGCAG[A/T]GGTCTGTACCAGTGG | 68519 |
| rs258979298 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108392725 | CCTCTAGGCCTTCCC[A/T]GCATTGCAGGAGAGG | 68519 |
| rs258981672 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474486 | GTCCAGAGAGTGTCA[A/G]TAGTTGCTGAATTTA | 68519 |
| rs258991790 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108419282 | CCCGTGATAGCTCAC[A/G]TTTTGTTTATCCAGT | 68519 |
| rs258997864 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450933 | taataaagagggatg[C/G]agggggctggtaggg | 68519 |
| rs259008628 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108526321 | ACACCCTAGACCTTC[C/G]GGTTGAAGAACTTTA | 68519 |
| rs259020460 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108432780 | CTGGCACTTTGCCAG[C/T]CATCAGCACCAGCAG | 68519 |
| rs259031640 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108465365 | ACTACATCAGAGGCA[C/T]ACACTACCCTCAGCT | 68519 |
| rs259037719 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108529706 | TACATCTCTGGCTAA[C/G]CCCAGTGCGTGTGTT | 68519 |
| rs259039122 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108517022 | GCAGCCTGTCTTCCC[A/G]GGACGAGAAGCCTGG | 68519 |
| rs259053152 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108514279 | CCGGGAAGGTGAAGT[C/T]GGTGGGGCTTGAGAG | 68519 |
| rs259060823 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532497 | CCTGCCTGCTGGGAC[G/T]GTGGGTGTGCACCAC | 68519 |
| rs259074576 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535593 | GAAAGTTCAGATGCC[A/G]GTGGGGGGCAGAAAG | 68519 |
| rs259076422 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108529252 | CCACTAATGCTTGTG[A/G]GGAGCTTGGGACAGG | 68519 |
| rs259094132 | in-del | -/T | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108400644 | GCAACAAAAATAATC[-/T]TATGGTTGGGGTCAC | 68519 |
| rs259106159 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108511277 | CCATTTTTGGCATCC[C/T]GATTGAATCCTTACT | 68519 |
| rs259119677 | in-del | -/ATAAATAAATAAAT | | | intron-variant | Eml1 | Mm_Celera | 12:108518029 | CCCATCTCAAAATAA[-/ATAAATAAATAAAT]AAAACAAAAGAAAAA | 68519 |
| rs259120549 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473620 | GTCAGCAGAGGCTGA[A/G]TGCCTGTGTCCTCCC | 68519 |
| rs259129328 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393975 | TGGCCTCTGGGAATC[A/G]GGATGTAAGATCACA | 68519 |
| rs259145477 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443608 | GCCCACTGGCATCTC[G/T]ACGCTGCTGCCTTCA | 68519 |
| rs259156679 | in-del | -/TTT | | | intron-variant | Eml1 | Mm_Celera | 12:108466471 | ACGATTAAGATGTGA[-/TTT]TTTTTTTTTTTAAAG | 68519 |
| rs259185300 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108491593 | TGGAGTCTTTCCCAT[A/G]ACTTCATACAATCTT | 68519 |
| rs259197649 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379677 | TATCCTTTATTATTT[A/G]TTTTTTTTTTTTGTG | 68519 |
| rs259199423 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449489 | CAGCCCTGTGTCCTC[C/G]AAAGGGTCTTTAGAC | 68519 |
| rs259209195 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108467795 | TCTATTAAAGCACGT[-/G]GATAGAGATGTGTGT | 68519 |
| rs259211692 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108398992 | TGTTCAGATGCTAAG[C/T]GTATGGCTTCCTGGA | 68519 |
| rs259221128 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447418 | TGGAGATTAGGTCAC[A/T]TAAGCCACCAGGGAC | 68519 |
| rs259224869 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476513 | TTAGACATTGTGTAA[A/G]ACAAAGGCCCACCCT | 68519 |
| rs259236753 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480408 | GTTTTTGTAGTATTG[A/G]CAATTTTTGTGGTAC | 68519 |
| rs259262654 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443755 | TGTGCCAGAGGATGT[G/T]CCTCAGTTCCCTGTG | 68519 |
| rs259280428 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108413702 | AGAGGGTATTAGGTC[C/T]CCTGGAATTTGAGTT | 68519 |
| rs259285128 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527932 | GTCAAAACTCAAAAG[C/T]GAAACTGAGTCCTTC | 68519 |
| rs259292516 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108379296 | TGTGTGTGTGGCCAC[C/T]GGTGCTTGAGCTCAT | 68519 |
| rs259295305 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108383830 | AAAATCATTAATTCA[C/T]CTAAACAGCATTAAT | 68519 |
| rs259313744 | in-del | -/TAT | | | intron-variant | Eml1 | Mm_Celera | 12:108524051 | CATCCTAAAGCAATA[-/TAT]ATATATATATACCTT | 68519 |
| rs259354381 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108479193 | GGGTCCCAGGCTTGG[A/G]CATACTGAAGTTTCT | 68519 |
| rs259398298 | in-del | -/GCCCAT | | | intron-variant | Eml1 | Mm_Celera | 12:108499113 | CACTTTCATCCTGTC[-/GCCCAT]GCATCCCACTTTTGT | 68519 |
| rs259416805 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108400003 | CATAGGCCGCCCTAT[-/G]TATGGCCATGAGAAA | 68519 |
| rs259418972 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108491892 | CACTAATCCACTAAG[-/A]ATTTTTTTTTTAACT | 68519 |
| rs259426915 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480725 | AGCTCCCATTAGGAA[A/C]GGTTTCTGATGGCAG | 68519 |
| rs259446637 | in-del | -/GGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461060 | ATAAATAGATTGATA[-/GGT]GATAGATAGGTAGAT | 68519 |
| rs259456105 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108494136 | GGCTCAGCTGAAGAG[-/C]CCCCTTTTTTAGCCC | 68519 |
| rs259456601 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374903 | GGACAAACCTGACAG[C/T]TGTCTCTGCCCTGGA | 68519 |
| rs259460348 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm33385 | GRCm38.p3 | 12:108400451 | ATGAATCTACGGAAG[A/G]GGGAGGGTGAACCAC | 68519 |
| rs259463233 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450762 | AGCGAGTGTGCACTG[A/T]GTGTTTCCCCCTCAG | 68519 |
| rs259464588 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108487857 | TGTGCACTGCACAGC[A/C]ACTGGCAGGTCTCTG | 68519 |
| rs259481987 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108388909 | GCTGGTCTCTCCTCT[C/T]TCCTAATGCTGGGAT | 68519 |
| rs259485453 | snp | C/G | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108421902 | GGTCAGAGCTCCGAG[C/G]CTGATAGCAGGCTCG | 68519 |
| rs259491224 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451935 | TCTGGATGTCTGTCC[C/T]CAGTGACCACTTTCA | 68519 |
| rs259502738 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108458662 | AAATCTCAGTAAGTA[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTATG | 68519 |
| rs259514209 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108497831 | ACTAATTTTATGGGG[G/T]GGGGGAAATCACCAC | 68519 |
| rs259528507 | snp | C/T | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108370363 | TTCTTTGAGCTGCTT[C/T]ACTTCATGGGTCTCA | 68519 |
| rs259545416 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108416734 | TGAAAAAGACTGATA[G/T]GTTTATGATTGACCA | 68519 |
| rs259555026 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417568 | GAAGCTTCAGGCATG[A/T]CGCAGGCAGACAGAA | 68519 |
| rs259562267 | in-del | -/CT | | | intron-variant, frameshift-variant | Eml1, Gm33385 | Mm_Celera | 12:108411081 | AGGAGGAAGAGCAGG[-/CT]CTCGGCAATGTGCAA | 68519 |
| rs259563829 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476713 | GGTTACCAGTACTGT[A/G]ATATCTTTATCACAG | 68519 |
| rs259564279 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108443290 | CTGGACTGGGGAGAG[-/T]TTTAGAACAGCCAGG | 68519 |
| rs259566507 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108380692 | GGACATAACCCCTCC[C/T]ACTCGGCTGTTTACG | 68519 |
| rs259577005 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108463768 | CAAATCAAAATGCCC[C/T]GAGCCCCACCCACTG | 68519 |
| rs259603163 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108521911 | AGGAAGCTCCACTCC[C/T]AAGCGCTTTAACACA | 68519 |
| rs259605313 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108514330 | AGTTTTGTTAAGCAT[A/C]CTAAGAGGCCTGCGG | 68519 |
| rs259649201 | in-del | -/AAA | | | intron-variant | Eml1 | Mm_Celera | 12:108499919 | GAGAAGGGAGGGGGG[-/AAA]ATCAAACATTCACAG | 68519 |
| rs259650533 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108504624 | CCCCTGTCTGGGTTA[A/G]ATATCATCGATTCTG | 68519 |
| rs259653181 | snp | G/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422208 | CTTGATAACTTTCTA[G/T]TCCATTATTATTATG | 68519 |
| rs259663655 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108482914 | CAGAAACTCTCTGGT[C/T]CTAAGAGCTCTGTGT | 68519 |
| rs259671477 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416395 | GCAACTTTATCTTTT[A/G]TTGGACAAACCTAGG | 68519 |
| rs259683717 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108385997 | CTGTACAGCCGAGAT[C/T]TCTCTCGCTTAGGGC | 68519 |
| rs259700441 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387944 | GATGTCTGCTGAATG[A/T]TTCTGTGCCAGCCTT | 68519 |
| rs259706510 | in-del | -/AC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451331 | TACATATGCAGATAT[-/AC]ACACGCACACACACA | 68519 |
| rs259743490 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108424369 | TGTATTTGGTATTCC[A/G]CCGATCACTGGGATA | 68519 |
| rs259749379 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484586 | AACTCTTTAAACTGC[C/T]ATGAACTTACCACGA | 68519 |
| rs259755950 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482438 | GCACACACACACACA[C/T]ACACACACACACAGC | 68519 |
| rs259765186 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387357 | TGTAAAATGTCCCTA[C/T]AGCCTCTTGTGTCTG | 68519 |
| rs259776285 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388208 | TACGCATCCTGCAGC[C/T]GCAACAGGCCTCTCT | 68519 |
| rs259792872 | snp | A/G | | | synonymous-codon | Eml1 | Mm_Celera | 12:108521354 | ACGGACAGTAGCCGA[A/G]GGGAAGGGCAACGTC | 68519 |
| rs259805440 | in-del | -/TAT | | | intron-variant | Eml1 | Mm_Celera | 12:108388728 | TTTGATATATATATG[-/TAT]GTGTGTGTGTGTGTG | 68519 |
| rs259822371 | in-del | -/GC | | | intron-variant | Eml1 | Mm_Celera | 12:108456330 | ACATATGTTAGGTAA[-/GC]ACTCTATACCCCATC | 68519 |
| rs259839964 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108394204 | AGACATCTTGACCCT[G/T]GGAATTCAAGACTGG | 68519 |
| rs259840022 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108492465 | ACACCTCTTCAGCCC[A/G]CCTCTTCTATTTCCC | 68519 |
| rs259885069 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108528955 | GGAGATGACATGGAC[A/G]GAATACTCTCCTTGG | 68519 |
| rs259904615 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403380 | GGATTAAAGGCGTGC[G/T]CCACCACTGCCTGTC | 68519 |
| rs259914357 | in-del | -/CT | | | intron-variant | Eml1 | Mm_Celera | 12:108432866 | AGAAGCCTGCAACTC[-/CT]CTCTCTCTGTCTCTT | 68519 |
| rs259921671 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454989 | TGAGTTGCCCTGACT[C/T]TCCTGCTCAGGCTTA | 68519 |
| rs259935992 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433780 | ACTCATGGCTCCCCA[A/G]CTCCAAAATCTGCTT | 68519 |
| rs259948627 | in-del | -/TTTTTTTTTTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108432025 | TAAAATGTCAACATC[-/TTTTTTTTTTTT]TTTTTTTTTTTCAGT | 68519 |
| rs259950735 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108452102 | CATTTAAACTGTTTC[A/G]CTTCTCCTGCATGCC | 68519 |
| rs259960401 | in-del | -/CACACACACACACACACACACACACT | | | intron-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108537722 | ACACACACACACACA[-/CACACACACACACACACACACACACT]CTCTGCCTACCTACT | 68519 |
| rs259980594 | in-del | -/AAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108477090 | TCATCAATCAAAAAG[-/AAAA]AAAAAAACATGCTGG | 68519 |
| rs259993310 | snp | A/C | | | synonymous-codon | Eml1 | Mm_Celera | 12:108534909 | CTGGTCCGTGAACTC[A/C]CAATTCCTGGTGTCA | 68519 |
| rs260004274 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108440732 | CGGCTGCCACTGAAC[C/T]GTGGCATCTCATCCA | 68519 |
| rs260013702 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402085 | TGGCCAGCATTAAAC[G/T]CATGGAGATCCTTCA | 68519 |
| rs260025049 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108508185 | AAGCCTGAAGCCCTG[A/C]GTTCAGTTTCCAGGA | 68519 |
| rs260058992 | snp | C/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536451 | TTTGCTTTTGTGAAA[C/G]TGCAGTGCCTGTGGA | 68519 |
| rs260065696 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440086 | TGAGAGACCAGAGTT[C/T]TGCTACCCAGGGCAC | 68519 |
| rs260074943 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408874 | GTTGTGGATCTCTGC[A/G]TTAACTGCTGATCAA | 68519 |
| rs260076168 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494141 | CAGCTGAAGAGCCCC[C/T]TTTTTAGCCCCCACC | 68519 |
| rs260076520 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108401555 | TCTGTGGCCAAGATA[C/T]TGTGCTTGGAGAGCT | 68519 |
| rs260084812 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429502 | TTAAACTTTCACACA[C/T]TCTCTCTCATGCGAT | 68519 |
| rs260091695 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418622 | gccagtaTtcttcct[C/T]tctctctctctctct | 68519 |
| rs260118666 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525868 | AAATGCAATATTTTA[C/T]CTTTTAATAATTGTG | 68519 |
| rs260134698 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408240 | GTGTGTGCCGCCACA[C/T]CTAGTGCCTCTTGAA | 68519 |
| rs260148575 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108535685 | GAAAGGCAGGGAGGA[A/G]AGGTAGCCAGTTCCA | 68519 |
| rs260185064 | snp | A/C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377449 | CGTGTGCCCTCCCTC[A/C/G]CCATGTGTAGGGCTC | 68519 |
| rs260205013 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108532012 | AGGGAGAGAGGGAGA[A/G]GAGAAGGGTGAGAGT | 68519 |
| rs260213838 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108506035 | TGAGTCATCTGTCAC[A/G]GGTGCCAAAAGCCCA | 68519 |
| rs260232355 | snp | C/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410079 | CACACTTGCACACAT[C/G]TACCACAGTGCGCAT | 68519 |
| rs260247969 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108513727 | ACAGGTGTTCTAATC[A/G]GATGTGTCTCCTGGC | 68519 |
| rs260257443 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496085 | TGTCTTCTGCAGGCT[A/G]GTGTCCAGGAGGAGG | 68519 |
| rs260267132 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108453897 | TCCCATATGCTAATA[C/T]ATGGGCTTTGTAATG | 68519 |
| rs260280263 | in-del | -/ACATGCACACAC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451330 | TACATATGCAGATAT[-/ACATGCACACAC]ACACACGCACACACA | 68519 |
| rs260295157 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417167 | GGAGGGTACCGACGT[C/T]AGAGATATGTATGCA | 68519 |
| rs260295335 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108409338 | AATGAAATGCAATTC[C/G/T]GACCCTCCCCACACA | 68519 |
| rs260299685 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108468224 | CCAGAAGGTATGGCT[C/G]ACTAACAGTGGATAG | 68519 |
| rs260305520 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379121 | GCTCCTCTGTATGTA[A/G]CCTTTCAACTTTTAA | 68519 |
| rs260329996 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108512709 | ATGCACATTTTTTTT[A/T]AAAAAAAGTAATCCC | 68519 |
| rs260345919 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108519437 | GTGTGTGTGCACATT[C/T]GACTGTGTGCATGCG | 68519 |
| rs260365700 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108475590 | GCACTCTGCTCTCAG[C/T]TTGGGAGTGAGTGTC | 68519 |
| rs260369818 | snp | A/G | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108538250 | TGGGAGCCCGAGGAC[A/G]CAGACTCGAGTTCCG | 68519 |
| rs260377074 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527273 | GAGGCTGGCATCTGG[A/G]ATCTCTATCTGCTCT | 68519 |
| rs260389935 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404772 | AACACACACATGCAC[A/G]TGCAAATACATACAC | 68519 |
| rs260400791 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372309 | CCCGGGAGGCCCTGT[A/G]GTATCTGACGGACAT | 68519 |
| rs260436511 | snp | A/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412682 | GTGAAGCTGGGCGTA[A/G]TGGCTCACACCTTTA | 68519 |
| rs260476120 | snp | G/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108411936 | GGGAGGGGGAGTTGG[G/T]TTTTTTTTTTTTTTT | 68519 |
| rs260479047 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108509628 | AAAAAAGTTTAGGCC[A/G]GGCGTGGTGGCACAC | 68519 |
| rs260484246 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108428832 | GCTACTGGGTATTAT[C/T]TTTCTCTCACCTTGA | 68519 |
| rs260497375 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108472768 | AGAGCAATCAGGGAA[A/G]ACTCCTGATTTCAAC | 68519 |
| rs260510866 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108399859 | GTTTCCCCTCTCCAA[C/T]AGTCACAGCCCCAAA | 68519 |
| rs260516783 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108524634 | TCTAGAACAAAAAGA[A/C]GCAAATACCCCCAAG | 68519 |
| rs260538928 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108528429 | CCAGCCTCCTCCACC[A/G]TGGGGTGGGCAGTAG | 68519 |
| rs260551914 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108497029 | TTCCCAAAACTCATA[A/G]AAAGAACTGGGACAT | 68519 |
| rs260560909 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108480152 | CAGTACAATCTTAAG[A/T]GGAGAGAAGGAAGGG | 68519 |
| rs260573083 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530969 | CTTTTGATGAGTTTA[C/T]TCTTCTAGATTTGTT | 68519 |
| rs260579151 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108503980 | AGGGATAAACGGCAA[A/C]TTGGGTGAGAGGTTA | 68519 |
| rs260587535 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108417974 | GCTGTGGCCCACCAC[A/G]CTCCATATTTTATAT | 68519 |
| rs260598461 | snp | C/T | | | intron-variant, missense | Eml1, Gm33385 | Mm_Celera | 12:108401306 | GGCTGGCTGATGTGA[C/T]TGATCCAAGGAACAG | 68519 |
| rs260617350 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108384259 | AGCACAACACAAAGA[C/T]AAATGCATCACTTCC | 68519 |
| rs260647092 | in-del | -/CACC | | | intron-variant | Eml1 | Mm_Celera | 12:108395928 | AAGAGCATGGAATTT[-/CACC]CACCTTCATAGGGAT | 68519 |
| rs260652769 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108516168 | GGAACAGCTAACTTA[C/T]CCAGGGACTTGGCCC | 68519 |
| rs260665050 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108454266 | TTTAAGTTTTACCTT[A/G]ACTCTATCTTAATGG | 68519 |
| rs260665199 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108461334 | TTCAGACAGTATTCT[A/G]GAATTTTGAAATTTT | 68519 |
| rs260676855 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455630 | TTCAGAGGTGGCACC[C/T]TCTGCTGAGCATGGT | 68519 |
| rs260696744 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108505638 | AATATCAAAAGATAT[A/T]TTTTGATTCCGAGAT | 68519 |
| rs260702382 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108478061 | GGGGTTATTAGGTAC[A/C]GAGGAGAAAAGAGAC | 68519 |
| rs260711271 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108419813 | GCTACAAAACACCCA[-/T]TTTTCCTTTCTTTCT | 68519 |
| rs260718621 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108395789 | CAGTCTCAGAAGCCC[A/G]TGGCAAGTACATCTT | 68519 |
| rs260758495 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108389817 | GAGAGAGAGCCCACT[A/C]GTAGGCAGTGCGACC | 68519 |
| rs260780635 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108535588 | GAATAGAAAGTTCAG[A/G]TGCCAGTGGGGGGCA | 68519 |
| rs260791425 | in-del | -/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370852 | TGAGTGAACTGAAGT[-/G]TGGGTGGCTGTGCTC | 68519 |
| rs260825556 | in-del | -/CAG | | | intron-variant | Eml1 | Mm_Celera | 12:108477018 | TTTTTTTTTACAACC[-/CAG]CAGCATCACCTGCAC | 68519 |
| rs260848635 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108436161 | ACTTAGGAACCCCAG[C/G]TGAGCACAATCGTGC | 68519 |
| rs260853538 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108501835 | TAATTTTAAACatat[A/G]tatatatacatatat | 68519 |
| rs260859796 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108430838 | AGTGGAAAACCATAT[A/G]TTTGCCGTGTTCTCC | 68519 |
| rs260864890 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402066 | GTGACTTACTGTGTA[A/G]CTCTGGCCAGCATTA | 68519 |
| rs260870824 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108520609 | TTGGTGGTGGTTGGG[-/T]TTTTTTTGGTTGGTT | 68519 |
| rs260871217 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108450380 | GGTGGCTTTGCCCTC[G/T]ATGTGCTAGGTGCTT | 68519 |
| rs260889508 | in-del | -/TTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108436836 | CTCTCTTTCTCTGTC[-/TTTT]TTTTTTTTTTTTTCC | 68519 |
| rs260892716 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108500284 | TGATCAGTAAAGTTT[A/G]AACAAGCCAAGTCTT | 68519 |
| rs260898289 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442177 | CAAACGTGGGGAAAT[C/G]GTAAAAATGGGCAGG | 68519 |
| rs260904757 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108504416 | CGTGGCTCTCATCTA[-/T]AAAGTCAAGCTACGT | 68519 |
| rs260921512 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108398286 | GTGTCAAACACAGGC[A/C]GGGAGAGAGATCTCT | 68519 |
| rs260928959 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447004 | TAGGCAAGGCTTACT[A/G]CTCCAGTAAGGCCAG | 68519 |
| rs260943947 | snp | C/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108539076 | CCAAGTGGGTCAAGT[C/T]GGAGAGGGACTCTTC | 68519 |
| rs260947150 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441816 | AGAGAGAATCCAGAA[C/T]CCTGAGCATGCATGT | 68519 |
| rs260971282 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108404100 | TCCTAGGGCTTTACC[C/T]TGAAAAGGCTGCGCG | 68519 |
| rs260995626 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108376130 | ACTGCAACCAGGAGG[A/G]ACCCGAATGTTTGAT | 68519 |
| rs260998539 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108453478 | CTGCCTCTGCCTCTC[C/T]AGTGGTGGGGTTACA | 68519 |
| rs261004824 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108488270 | ACTGTCCCTTCTCAT[A/C]TGCCTGCCCTCCCTG | 68519 |
| rs261019915 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108424225 | ACGAGAGCATTAAGA[G/T]GAACAAATGTGTTGA | 68519 |
| rs261069833 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108432489 | GAGCAAGCAAAAGTG[A/G]ATATGGGAACCAGAG | 68519 |
| rs261081859 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477444 | GTCTAGTGTGTAAGT[C/T]GACAAAAACTAGCCA | 68519 |
| rs261093864 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108371828 | GGCTGCATGGAGGTG[A/G]CTGGGGATACAGGTG | 68519 |
| rs261098617 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108528913 | CTGCTCCCTCCTGAG[A/G]AGAGGTCAAAGGACT | 68519 |
| rs261107987 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108379254 | GTGTGTAGGTACATG[-/GTGTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGGC | 68519 |
| rs261141655 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108378172 | GAGATTATACAGTCT[A/G]AATAAGCACCGGAAG | 68519 |
| rs261147361 | in-del | -/CACC | | | intron-variant | Eml1 | Mm_Celera | 12:108497524 | TGCCTTTGGCCAATA[-/CACC]CACACACACACACAC | 68519 |
| rs261169789 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438944 | AAGGAGAAAAGATGG[C/T]ACAGAAAATTGCATC | 68519 |
| rs261215491 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438302 | CAGGCTAAGCCGTGT[G/T]CTCAGCACACAGACA | 68519 |
| rs261216945 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108444063 | AGACCTTGCTGCATG[A/G]CAAATTATTTTCTTG | 68519 |
| rs261246295 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437122 | GCTTTGTCTGATGCT[G/T]TTGAGATGGCGAACT | 68519 |
| rs261249207 | snp | A/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412609 | TAGCATAGGTGCTGG[A/G]ATGGCAAGAAGAATT | 68519 |
| rs261264945 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443704 | CCGGGATGGCTGTTT[A/G]TCTCTTGCACACCCA | 68519 |
| rs261271352 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108535907 | tgtgtgtgtgtgtgt[A/G]tgtgtgtgCTTGTCT | 68519 |
| rs261271429 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532887 | TTGTGGCTTTTCCAG[G/T]GCTACTTGCAAGTAG | 68519 |
| rs261276327 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108459763 | ACAGATAGATATAGG[A/G]TGAAACAGACAAGCT | 68519 |
| rs261294199 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108486781 | ATACCACTTTGTAGA[-/C]CAGGGTAGCCTTGAA | 68519 |
| rs261301369 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108383597 | TCAGACACACCAGAA[A/G]AGGGTATCAGATCCC | 68519 |
| rs261319275 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108492767 | AGACTAGTTCAGCAT[C/T]CTTAACAATGCTAAG | 68519 |
| rs261336904 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108427323 | GAATAGGAAGGAAAT[-/A]AGAGTTGTAGGTCCA | 68519 |
| rs261339818 | snp | A/G | | | downstream-variant-500B, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108539861 | GTTGAAGGAATACTT[A/G]GGTATCAAGGAAGGG | 68519 |
| rs261343608 | in-del | -/TGCC | | | intron-variant | Eml1 | Mm_Celera | 12:108463302 | CTTAGAAAGATGAAG[-/TGCC]TGCCAGTCTAGACGT | 68519 |
| rs261347870 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108389385 | GATTGGCCTCTAAGT[C/G]CGCATTTGCGGCCTC | 68519 |
| rs261354425 | in-del | -/CTGGTGC | | | intron-variant | Eml1 | Mm_Celera | 12:108511374 | ACCACATGCTGGTGT[-/CTGGTGC]CTGGCAACTGGCTAT | 68519 |
| rs261375487 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108378296 | CGAGGTTGACACTCA[C/T]GAGAATGGCCTCTTG | 68519 |
| rs261402662 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486128 | CTGCTTGTAGCAGGA[A/G]CAGAGACTGCTGCCT | 68519 |
| rs261429193 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108454212 | TCGGCTTTCTCAAAA[C/T]TACCTCCTTCCAGGG | 68519 |
| rs261446517 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108503794 | TAGCTCTCTGGCTTT[C/G]GGAAATGCCATTGTA | 68519 |
| rs261455048 | in-del | -/TCCAGTAC | | | intron-variant, frameshift-variant | Eml1, Gm33385 | Mm_Celera | 12:108401071 | GGGGATGGGAACAGT[-/TCCAGTAC]TCCAGTTCTCTCTCC | 68519 |
| rs261456509 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108434556 | TTAGCTGTGGTTGTT[A/C]GTTGGAGTCCTGTAA | 68519 |
| rs261480839 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108479608 | CTTTGCTTTTTGGTA[A/G]GCATATTTTATTGCT | 68519 |
| rs261485075 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438258 | GATTTTGTTTCCCTA[-/T]TTTTTTCGCTCAACC | 68519 |
| rs261495799 | in-del | -/AAA | | | intron-variant | Eml1 | Mm_Celera | 12:108522472 | GCAAGATTCAGACCT[-/AAA]AAAATCACTTCTCAT | 68519 |
| rs261501261 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108493174 | TTCAGTTTACAGTTC[C/T]AGGTTAGGGTCTGTC | 68519 |
| rs261505830 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108440991 | TGGATCGGGTTCACC[A/T]TCTCCTGCTTCATGT | 68519 |
| rs261508460 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486473 | TGAGAGGGCTGTCTT[A/G]AGCACTTTTTATGAA | 68519 |
| rs261514516 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108510493 | GGCACACATCTTTAA[C/T]GCCAGAGTTCAGGAG | 68519 |
| rs261517526 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108396460 | TTCCTTGGCTGTGGC[C/T]ACACTGATGGCCAAT | 68519 |
| rs261531835 | snp | C/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108536890 | TTTCCCTATTTCCTG[C/G]TGTTCTGCCTACTAA | 68519 |
| rs261572490 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108497827 | ACAAACTAATTTTAT[-/G]GGGTGGGGGAAATCA | 68519 |
| rs261573883 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369591 | GACCTTGTGATCACA[A/G]CCCTCTGTGGCCTCT | 68519 |
| rs261578376 | snp | C/T | | | intron-variant, utr-variant-3-prime | Eml1, Gm33385 | Mm_Celera | 12:108401003 | GGGCAGGGCCTCAGG[C/T]TCAGTCCCAGCCCGC | 68519 |
| rs261586028 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449223 | ACCTTCTCAGTGCTG[A/G]GTTACAGGGCCACCT | 68519 |
| rs261590665 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108440285 | AAAATGGCCCCAGGG[-/T]TTTTTCTATATTGCT | 68519 |
| rs261592306 | in-del | -/GG | | | intron-variant | Eml1 | Mm_Celera | 12:108371892 | TATACCCTGATGTGT[-/GG]GTAGGATTAGCTACC | 68519 |
| rs261636293 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455499 | AGACTATGGTGGCAG[C/T]GGAGGAGTTGCTCTT | 68519 |
| rs261644304 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108436089 | TGCGGCCCTGCTCTC[C/T]TTCCCTCCCCCTGCC | 68519 |
| rs261648400 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504990 | TGGCATGCATGTGGA[A/G]CATATAGTCATATTC | 68519 |
| rs261652308 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108481658 | GACTGAAGACTAAGA[C/G]CCTGGGTTTCGTTTT | 68519 |
| rs261656232 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108399834 | CCAAGGTGGACCATT[C/T]CTCCATCCAGTTTCC | 68519 |
| rs261660324 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532104 | CACTGCGCATGCTGA[C/T]ATTTAGTAACCTTCC | 68519 |
| rs261686393 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108387787 | TAAAAGCTTCTGATG[-/T]TCTACATTTGACCTG | 68519 |
| rs261694495 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475494 | ACACACATACCAACA[C/T]GCCGTGGTGGTCCAC | 68519 |
| rs261699350 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488436 | GTAAGGAGGGCCCTG[C/T]TGCCTGTACCTTCTT | 68519 |
| rs261701981 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108374542 | TGCTCTATCAAGGTC[A/T]GCTCCCTTCATACTA | 68519 |
| rs261707887 | snp | A/G | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108539013 | CGATAAATTGCCCAA[A/G]GCTGGGCCTTGCTGT | 68519 |
| rs261761290 | snp | A/C | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403798 | TCCCAGCAACTCCAG[A/C]ACATGATGCCCCCAA | 68519 |
| rs261769511 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453579 | GCTCCACCCATTGAG[A/C]CATGTCCCCAGCTCT | 68519 |
| rs261772852 | in-del | -/A | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460996 | AAGAAATCCTGTCTG[-/A]AAAAAACCAAATACA | 68519 |
| rs261777583 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452487 | TCAGATGTGCATAAC[A/G]GGCAAAGCACAGGCC | 68519 |
| rs261791798 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108459115 | ACAGCAATAGAAACA[C/T]AGCTAAAATAGTCTC | 68519 |
| rs261804532 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108508549 | CTTCTAAAAATCAAA[A/C]AAGTCTTCATTTTAA | 68519 |
| rs261814347 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108388294 | GACCCACCTGATAAT[C/T]CAGGATCATCTCTTC | 68519 |
| rs261835785 | in-del | -/ATAC | | | intron-variant | Eml1 | Mm_Celera | 12:108432249 | GAGTGAAGAGTAGAG[-/ATAC]AGGAGGATGGAGTGA | 68519 |
| rs261835809 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108439554 | GGGATTTGAACTCAA[A/G]ACCTTTGGAAGAACA | 68519 |
| rs261841411 | in-del | -/CG | | | intron-variant | Eml1 | Mm_Celera | 12:108470580 | GGAACCCAAGTCCTC[-/CG]CAAGAGCAACCAGTG | 68519 |
| rs261849429 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376605 | CTGCTCCTCCCTGTC[-/T]ACCTCCATTCCATCC | 68519 |
| rs261851263 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484997 | AAGACCATGTGTGAA[A/C]AGGATCGTGCTCTGT | 68519 |
| rs261859936 | in-del | -/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108528213 | CTTAGGTCATCACAA[-/C]ATGAGGAACTATATT | 68519 |
| rs261889297 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108385575 | AGGGTAGCAATTTTC[C/T]TGAAATATCGCTCAT | 68519 |
| rs261897105 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108383234 | TTTAGACAGAAAGGT[C/T]TCTATGCAAGAAGAA | 68519 |
| rs261918096 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433666 | AACGCACTCGGCTGC[C/T]GCTCCCCAGGGAGGG | 68519 |
| rs261919352 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108478707 | CGTGCGCCACCACGC[C/G]CGGCTTCTGGCTTTT | 68519 |
| rs261949683 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108440679 | ATCTAACCTGTGCCC[A/G]GATCAGGGACTCAAA | 68519 |
| rs261966803 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108460072 | ACTGGGCTGACAGCA[-/G]GTCTAAGTGATCTCA | 68519 |
| rs261981092 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108456657 | GAGACAACGGTAACT[C/T]GATCGATCACTGGGT | 68519 |
| rs261986220 | in-del | -/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | Mm_Celera | 12:108537315 | TGAAGTTTCCAGTGC[-/T]CTCTGTGCTCTGTTC | 68519 |
| rs261990342 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108416190 | GAAAGTTGGATTATG[G/T]AAAATACAATGATAC | 68519 |
| rs261993918 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108534033 | CTCCACTGAGGTGGA[-/C]CCCCCAGGAGGATAT | 68519 |
| rs262003482 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108462775 | ACAAGGAAGGTGTCC[A/G]GGGCTGGGAACTGTG | 68519 |
| rs262016440 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108429154 | GCGCGCGCGCATGCG[C/T]GCGCGCATATGCATG | 68519 |
| rs262022795 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108514096 | GGGTCCTTCATAGGG[A/G]CCCCAGTCACTAGAA | 68519 |
| rs262027882 | in-del | -/GTG | | | intron-variant | Eml1 | Mm_Celera | 12:108378650 | GTAGTAGTAGTAGTA[-/GTG]GTAGTAGTAGTAATT | 68519 |
| rs262033695 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472736 | CCTGAGAGACCCTGC[C/T]TCAATGAATAAGGTG | 68519 |
| rs262050318 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108435608 | TGGAAATACTAAGCG[A/G]GAGCTTTAATCTTCT | 68519 |
| rs262067036 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108439475 | CACTATAGCTGTCTT[C/T]GGACGTACCGGAAGA | 68519 |
| rs262068923 | snp | A/C | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403043 | CGCACAAGAGATTCT[A/C]TCCACAAGCCCCAGC | 68519 |
| rs262098766 | snp | C/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108538233 | GAGTCATTTAGTCCC[C/T]GTGGGAGCCCGAGGA | 68519 |
| rs262124389 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108507663 | TCTGTTGTTCAATGC[A/T]GTATTCATTTCCACC | 68519 |
| rs262148253 | in-del | -/CTTT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480381 | TCCCTTCCTTCCTTC[-/CTTT]CTTCCTTCCCCGTTT | 68519 |
| rs262151008 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108463827 | TGTTGGTGTGCTTTG[A/G]GTGAGTTGTCCTGTG | 68519 |
| rs262168456 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108515695 | CATGCGCACAGATCA[A/G]ACCTTTTTTTTTTTT | 68519 |
| rs262182517 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462538 | ACACAGAGCACACTA[C/T]CAATGCCACTAAGTT | 68519 |
| rs262189908 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108381530 | AGAAGACCATGTACT[C/T]GCCAAGGAGAGACTA | 68519 |
| rs262216533 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108382024 | TGCCTGGGGAGGCTG[G/T]CCCAGAAAGATGAGG | 68519 |
| rs262236209 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520447 | GACCACTTTGAAGTT[A/C]AAGGAAGTTTTGGCA | 68519 |
| rs262238841 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433088 | ATACAGGGCCGGCAC[A/G]TCTTACTGTGAGACG | 68519 |
| rs262240714 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108406299 | CAGTGACTTCTTTGA[C/T]TTCAGACTCTGCACA | 68519 |
| rs262249302 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108377902 | AGGCTCTGTATTTTT[-/A]TTTTTTTCACTGTGT | 68519 |
| rs262268904 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108497201 | ACTATCCTGGACTAC[C/T]CAGCCTGACCCTACC | 68519 |
| rs262274869 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108414563 | ACAAAAATGAGCCAG[A/G]TGAGGGGTCGAACTT | 68519 |
| rs262287997 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461684 | ACCACCCACAAGGGG[A/C]CCTCCCCCCTTGATC | 68519 |
| rs262304942 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108431609 | AGACAGGTGCACACA[-/T]TTAACACGCTTATGC | 68519 |
| rs262305371 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437729 | ATGAATGTTAGATTC[C/T]GGTGCCTCACCGCAT | 68519 |
| rs262308299 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108483108 | AGAGATTTTTTATCA[G/T]GTCTGATATTCAAAG | 68519 |
| rs262318268 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108466472 | ACGATTAAGATGTGA[-/TT]TTTTTTTTTAAAGCA | 68519 |
| rs262320632 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108511730 | TTGTTTGGCAAAACC[A/G]AAGTCACTGTCAAAA | 68519 |
| rs262350187 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108490957 | TCTTCCTTGTGTGTA[A/G]CATGAAGGTGATTGA | 68519 |
| rs262383144 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108420777 | GATGCCAGGACTGCC[A/C]GTGGGAGCTACCACA | 68519 |
| rs262389911 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108486037 | CCAGCCAGCCGGCCC[C/T]TCTTCCCCTGCGCCC | 68519 |
| rs262397767 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466349 | TCAGTCCCCATGAGA[C/G]CTGGCTTGCATCCAT | 68519 |
| rs262402723 | snp | A/T | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108536337 | GGTAGGGGTCCGAGT[A/T]TGTCATTGCCTTTGA | 68519 |
| rs262411536 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108385614 | AGGTTTGGCCATTTG[C/T]TTCTGGGGATGTGGT | 68519 |
| rs262417352 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108518137 | GTTTTTGCTCTTGCC[A/G]AAGACCCAGGTTAAG | 68519 |
| rs262419639 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108436616 | GTGCTGGGCTGGGAA[C/T]TGGGGGTTGGAGGAC | 68519 |
| rs262459438 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402609 | ACTGAGCCACATCCT[C/T]GGCTGTTATTAGTTT | 68519 |
| rs262462915 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525954 | GAGTTAGCGTTTCCT[A/G]GCAGGGCTGTCAGCG | 68519 |
| rs262473742 | in-del | -/ATAT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474023 | AGAGAGAGAGAGAGA[-/ATAT]GAATGCCTGCTTGCT | 68519 |
| rs262481029 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492614 | AGGGCTCATGAGACA[C/T]TTTCCACGTGCCCGA | 68519 |
| rs262492613 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409864 | TACTCTCTCTCTGTG[C/T]CTCTCTGTCACACAC | 68519 |
| rs262504443 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520943 | TACACACATGCACAT[A/G]CTCTTGAGTGTGCAC | 68519 |
| rs262510013 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457826 | CTTGTGCCCTGAGGC[A/G]TGGTGGGAACCGGAT | 68519 |
| rs262516929 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108380885 | GGAATCATGTTACTC[A/G]AGATAATATTGAGTC | 68519 |
| rs262521323 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108507197 | CCTCCCTCCTTGATC[A/C]CTAATTGAGAAAGTG | 68519 |
| rs262527349 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108532212 | TTTGGATACAGGGTC[-/TT]TTTTTTTTTTAAGAT | 68519 |
| rs262558966 | in-del | -/GACT | | | intron-variant | Eml1 | Mm_Celera | 12:108500571 | AGCTTGCCCCAAGCC[-/GACT]GACTCTTCTTGCTTC | 68519 |
| rs262563270 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437921 | TCCTTGCTTCCCAGC[C/T]GGGATTCACACACCC | 68519 |
| rs262579255 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108483588 | TTTTTTCTTCTTCTA[C/T]AAATAGGACAATAGT | 68519 |
| rs262587889 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416004 | CATCCCAAAGAGAAG[A/G]GATAGCAGAAACATC | 68519 |
| rs262598533 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443427 | TGCTTTGTTCAGCAG[A/G]AATCTGTGTGTCCTC | 68519 |
| rs262614027 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442262 | CAGGGTGTGTCTGCC[A/T]GCACTCACAGATGTG | 68519 |
| rs262616039 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108488816 | GGAATGCTTAAAGCT[C/T]GTAGCAATACTTTCT | 68519 |
| rs262627690 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108491255 | CCGCCCTGATCTGTG[A/G]ATTCAGATGTAATGC | 68519 |
| rs262639495 | in-del | -/ATAG | | | intron-variant | Eml1 | Mm_Celera | 12:108484532 | TGCCATAGCGGGATA[-/ATAG]ATAGATGCTCCTTAC | 68519 |
| rs262660066 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108496416 | CAAGGGAAGCAAGGG[A/G]TCATATCCCTGATAC | 68519 |
| rs262727975 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108516664 | TGATGCCTTTGCTGG[A/C]CGTTTGGATTCGCTC | 68519 |
| rs262747326 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108419563 | TTTCAATTCTTCTAA[A/C]CATATTAACAAAAGT | 68519 |
| rs262749685 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108524347 | CCTATCAGATTACCA[A/C/T]GGCCTAAGGCTGATC | 68519 |
| rs262757998 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108432583 | GTGGGTGACAGCATC[C/T]GCACTTGGGGAGGGA | 68519 |
| rs262763593 | in-del | -/AACT | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108536102 | AGCCATCTCCAGACA[-/AACT]AACAGCTGTGTACAC | 68519 |
| rs262771768 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108465725 | AGTGGAAATCGTCAT[C/T]GGTTTGAAAGACACT | 68519 |
| rs262788298 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108517318 | GATTTGGTATTACAC[C/T]TTTTTATATATTTGT | 68519 |
| rs262794981 | in-del | -/CT | | | intron-variant | Eml1 | Mm_Celera | 12:108519691 | TTGTGTTTTTGTTTG[-/CT]TTTGGTTTTTTTTTT | 68519 |
| rs262816524 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406130 | CCTCTCCCTTCCCCT[C/T]CCCCACAACTTTTCT | 68519 |
| rs262824108 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108440583 | TGGTCTCATTTTCCA[A/G]CTCTCGCTGCTCATC | 68519 |
| rs262854063 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108414231 | TTTGTGTCTAAGAGA[A/G]AAGGCCCAGAGCCCC | 68519 |
| rs262861894 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108445758 | AATGATTTTTTAAAA[A/G]CCGATAAAAGCAATT | 68519 |
| rs262878338 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108493639 | GAAGTTAACCGTCAC[A/G]GAAGCATTTGGAGTT | 68519 |
| rs262880662 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108511475 | AAACCCTTTCGCGAT[A/G]ATGGATCTGTTGACT | 68519 |
| rs262890156 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108467513 | GCCTCAGCTAGAGTC[A/G]GCACACGCACAGCCT | 68519 |
| rs262901769 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518960 | GATGGGCACATTCTT[A/G]GGTCCTTTCCCTTGG | 68519 |
| rs262948385 | in-del | -/TGCC | | | intron-variant | Eml1 | Mm_Celera | 12:108390611 | GCCTCGTCCTGGCTT[-/TGCC]TGCCTCTAGCTCTGC | 68519 |
| rs262971018 | in-del | -/TGACGATGAG | | | intron-variant | Eml1 | Mm_Celera | 12:108465628 | GTTTTTTATTTTACT[-/TGACGATGAG]TGACGAGTGACAAAC | 68519 |
| rs262971727 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441672 | TGATTGTCACTTAGC[A/G]GCAATTTCAGACTCA | 68519 |
| rs262987236 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108487583 | AAAAATAGTACTTAA[A/G]TTGCTGTTTGAGTTA | 68519 |
| rs263004277 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108534380 | CATGTGGACAAAATA[C/T]ACATACATAAAAATC | 68519 |
| rs263004582 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108447059 | GGTCCAGATGGGTAT[G/T]AGCTAGCACGTTCTT | 68519 |
| rs263005768 | snp | C/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370722 | GCAAAGCTTCCTATG[C/G]CTCGGAGACAGACAG | 68519 |
| rs263016836 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417809 | TTTCATTTTACAGAG[C/T]GTTTATCATGCGTGG | 68519 |
| rs263046150 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108515955 | TCATGAGTCTTCTAG[A/G]TTCAGGAAGGTACAC | 68519 |
| rs263049597 | in-del | -/GTTTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108439218 | AGTGAGTTTTAGTTG[-/GTTTTT]TTTGTTTTTGTTTTT | 68519 |
| rs263096113 | snp | G/T | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | GRCm38.p3 | 12:108411619 | GCGTTGACTTGGCTC[G/T]TGGGTTCTCTGCTAG | 68519 |
| rs263103079 | in-del | -/GTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108535887 | TGAAGAGGCTGAGGG[-/GTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs263110892 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108425070 | GACATGGCTGTTATC[C/T]AGAGATGTCGTAGGA | 68519 |
| rs263118322 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108371894 | ATACCCTGATGTGTG[G/T]AGGATTAGCTACCTG | 68519 |
| rs263131876 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418589 | CTCCAGCCTTTGTCA[A/T]GCTGACACACAACAC | 68519 |
| rs263132592 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108388520 | TCTGGAAGGAGCGCA[A/C]ATTCTTCCCTAGGTG | 68519 |
| rs263134397 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108470532 | TAACTGGAGTTGTGG[A/C]CAGTTGTGAGCCACT | 68519 |
| rs263135668 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108371576 | CTTTAGCAGGAAGCC[-/G]TACCTCTAACAAATT | 68519 |
| rs263141090 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108439918 | CAGGTGAGACAGAAG[C/T]CTTGCTTTGAGGGCA | 68519 |
| rs263151855 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108394399 | AATTTTTAATTTACC[A/G]TATGGTATGTGTGTG | 68519 |
| rs263160797 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108443976 | GCATGGAACATGCAT[A/C]TTAAAGCATCGCATC | 68519 |
| rs263169765 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108492296 | GCTGGGCAGGCCATG[A/G]ATTTGTCCTTTGGCT | 68519 |
| rs263203863 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108450137 | GAAGACTCTAAGCAC[C/T]GGGGTCACCGTCTCG | 68519 |
| rs263209694 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525378 | GAATATATTTCTTAA[A/T]GGTTCATTTTTAATA | 68519 |
| rs263285381 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108415481 | CAACTCCAGGGTACA[C/T]GACACCCTCTTCTGT | 68519 |
| rs263297042 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486608 | GAATTTGGAGGATGG[A/G]AACATTGGATGCTCT | 68519 |
| rs263311408 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446415 | GTAACTTCTGAGAGT[C/T]GATGCTGTTGTTTTC | 68519 |
| rs263312870 | in-del | -/GT | | | intron-variant | Eml1 | Mm_Celera | 12:108488119 | ACAAAGTGTGCAGAG[-/GT]GTGTGGGAGTGATCC | 68519 |
| rs263348271 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469085 | GGTCCCCAGAGCTCC[A/G]GAACATTGTGGACAG | 68519 |
| rs263354731 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519902 | CACTGATCCTTAGCA[C/T]GTACACAGGAAACAC | 68519 |
| rs263363865 | in-del | -/GGGGAGGC | | | intron-variant | Eml1 | Mm_Celera | 12:108530176 | TGTAGAGAAAGCTGT[-/GGGGAGGC]GGGGGAGGGGGTTTC | 68519 |
| rs263384733 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469010 | GGATGTGACAGTCAG[A/G]ATGGTAAGGACAAGA | 68519 |
| rs263400441 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108519583 | GCCCCGCCCCTGGGA[A/T]CGGCCCACTTCCTTC | 68519 |
| rs263409322 | in-del | -/CA | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405093 | GCCAGGGGTAGGGAG[-/CA]CACACAGCTGGATCA | 68519 |
| rs263425900 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369447 | CACGACATGGGCCAG[A/G]CCAGAGGAGCCTTTG | 68519 |
| rs263429102 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108476304 | TTTGTTTGCTTGATC[A/G]TTTACTTTGACACTA | 68519 |
| rs263436971 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532296 | GAAGAGAGCATCAGA[C/T]CCTTTTACAGATGGG | 68519 |
| rs263444436 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527783 | AGCATCCACCCTACC[C/T]GCCGCTGCCCCGCAA | 68519 |
| rs263472589 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108463292 | ACGGGCTTGCACTTA[A/G]AAAGATGAAGTGCCA | 68519 |
| rs263480006 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108392762 | GGGAAAGAGCTGTAA[A/G]CCTAACCGGCTGCAA | 68519 |
| rs263485061 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108425598 | AGCCTCCAGGCTCCT[A/G]AAAAGGCTGTCCATG | 68519 |
| rs263491646 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108442682 | CTCTTAACTGCTGAG[C/T]CATCTCTCCAGCCCT | 68519 |
| rs263495468 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108470777 | AGGAGGGCCCAGTCC[A/T]TGTAACATCACCATC | 68519 |
| rs263500077 | in-del | -/TA | | | intron-variant | Eml1 | Mm_Celera | 12:108439631 | ATAGCACCCTTTTTT[-/TA]TTTTCTGGAAAACTT | 68519 |
| rs263500147 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478324 | TTCTGTGGCTTTTGA[-/T]TTTTTTTTTAAGATT | 68519 |
| rs263521816 | in-del | -/GTTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108481663 | AGACTAAGACCCTGG[-/GTTTT]GTTTCGTTTTGTTTT | 68519 |
| rs263525064 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108521788 | CATAGAGGTAAGTAA[A/G]TGTGCGTGCTGCATT | 68519 |
| rs263556119 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108497350 | AGCTCCTGATTGGCT[A/G]GCATTGTCTGCACCA | 68519 |
| rs263564464 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108424146 | AACAACTGGAGAAAA[A/T]TTACATTGCAGTTGT | 68519 |
| rs263566008 | in-del | -/GTGG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108481225 | TAGGGGTAAGGGGGT[-/GTGG]GTGGGTGGGTGGGTA | 68519 |
| rs263577150 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108504272 | ATGTAAGGTGACGTG[A/G]GGGAGCATTAAGAGA | 68519 |
| rs263617349 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108394232 | TGGCATGGGCAACAA[C/T]GGCGAGGCCCTGTGT | 68519 |
| rs263626649 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443762 | GAGGATGTGCCTCAG[G/T]TCCCTGTGCCATACA | 68519 |
| rs263634418 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503676 | TAGTCAGCAATATTT[A/T]ATGGCGAGATAAGGA | 68519 |
| rs263636781 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108525838 | CAAAACAAAACAAAC[-/A]AAAAAAAGAAGTCTA | 68519 |
| rs263645047 | in-del | -/TTG | | | intron-variant | Eml1 | Mm_Celera | 12:108447211 | CACAGGGTGACACAC[-/TTG]TTGTTGTGATCGGCA | 68519 |
| rs263651663 | in-del | -/TT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456693 | ACTAGAATCCTAATA[-/TT]TTTTTTTTTTTTTTG | 68519 |
| rs263666235 | in-del | -/A | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369297 | AGGGGGAGGAGGGGG[-/A]GGAGGAGGAGAGGGG | 68519 |
| rs263671985 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419482 | TGCATGTGGATATGC[A/G]TAATGCTGTCTTGCC | 68519 |
| rs263682884 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108378759 | CATTGTGTAAACCGT[A/G]GCTAGCAGACGGGTG | 68519 |
| rs263708309 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473572 | GCCATGCCATCTGGG[C/T]GCAGGCCGTGCCTTC | 68519 |
| rs263712297 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525266 | TGGCTGTCCTGGAAC[A/T]CACTTTGTAGACCAG | 68519 |
| rs263725154 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480376 | CCTCCCTCCCTTCCT[C/T]CCTTCCTTCCTTCCC | 68519 |
| rs263729925 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108449734 | GCATGTGTGTGTTTC[A/G]CATGACGTGGAACAT | 68519 |
| rs263761108 | in-del | -/TCAGT | | | intron-variant | Eml1 | Mm_Celera | 12:108429392 | AGCTATGACTTCTGG[-/TCAGT]TTTTCGAAATGACTA | 68519 |
| rs263786041 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108506157 | AATTGAAAGGGACAT[-/G]GGGGGTGGGGGTGGG | 68519 |
| rs263823880 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108375262 | AGAGCCTGAGTCTAG[A/G]GGTGCAGGGCATTTA | 68519 |
| rs263832637 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | Mm_Celera | 12:108422257 | TCTGGAAGTTAATAC[C/T]GAAAACTTCAGAATT | 68519 |
| rs263852768 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108398729 | AAAGTCCAGCACCCA[A/G]ATCATGAAACGACAG | 68519 |
| rs263854354 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393068 | GCAGCCTTAGGTAGC[C/G]TGAGAGTCTGAGGTC | 68519 |
| rs263864576 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108442904 | ATATCAGTAAACCCT[A/G]AGGAATGTTACCAAG | 68519 |
| rs263868289 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108447240 | GGCAGTGGCTGATCC[A/G]TCATCTTCTATAAAC | 68519 |
| rs263876375 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108495731 | GGAATGTGGGTGAGT[A/G]TAGCAAGAGACGTTC | 68519 |
| rs263880053 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453605 | GCTCTTCGTCAGCTC[C/T]TAGTCAGAGCTTCGT | 68519 |
| rs263890224 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108526678 | CCAGGCCAGGTTGTT[C/G]CATCGCAGCACCATG | 68519 |
| rs263897139 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108531990 | GGGAGGGAAAGGAAC[-/AG]AGAGAAAGGGAGAGA | 68519 |
| rs263901575 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108519667 | gttttgtttgttttg[G/T]tgttttgttttgtgt | 68519 |
| rs263947075 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108372054 | ACACACCTACCGTGC[A/G]GTTTGCGAAAATTAT | 68519 |
| rs263958947 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108419033 | TTTCATCATTCCAAA[C/G]TGTGACTGTGACCCC | 68519 |
| rs263983794 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108447678 | AGTGGAATGGCTTCT[C/G]ATGTCCCTATCATGA | 68519 |
| rs263996905 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108496361 | AGGCTTGTTTGAGCC[C/T]CACCACCCACTCCAC | 68519 |
| rs264012090 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471479 | GGGAGCAAGGGAGGA[A/G]GAGCAGGGGAGAAAG | 68519 |
| rs264032313 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524396 | AACAGAAAGCCCACA[C/T]ACACATAGAAGCTGA | 68519 |
| rs264032425 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108384471 | CAGGGCTCACAAGTC[C/G]TTACAGAGGGAGGCG | 68519 |
| rs264061923 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108478438 | TTATACATAAGTACA[C/T]TGTAGCTGTCTTCAG | 68519 |
| rs264069590 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108530137 | CTGAAGAGCTTCGAG[C/T]GTTTGTCAATATCCT | 68519 |
| rs264079512 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108373820 | GCCTTAGGCCTGGGC[C/G]GGCAAGCCTACAGGA | 68519 |
| rs264081630 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108414493 | AAGGCAATGGTTCAG[G/T]TGGCAATGTGCTCAC | 68519 |
| rs264092749 | snp | C/T | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108536013 | ATGGGAGAAGCCAGG[C/T]TGGTGGAAGGGAACA | 68519 |
| rs264102291 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108466560 | GGAAATCATTTCTCC[C/T]AGTAACTGGGAGACA | 68519 |
| rs264110042 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108433825 | CTGCTTCAGTGGAAT[-/A]AAAAATGTGTTCAGA | 68519 |
| rs264114521 | in-del | -/AAATAAAT | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370280 | GTACTCATAGACATA[-/AAATAAAT]AAATAAATAAATAAA | 68519 |
| rs264146274 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474317 | CAGGACAACCAGGGC[A/T]ATACAGAGAAACCCT | 68519 |
| rs264151748 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108526038 | CCCGTGTCCTGTGAC[A/G]GCACATCTTACATAG | 68519 |
| rs264165661 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402527 | GTCACAGTCAGGCAC[C/T]ACACCAAGTTTATGT | 68519 |
| rs264206877 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457534 | ACTGCAGTATTTAAC[G/T]GACTTCCAGACATTT | 68519 |
| rs264218892 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108507056 | CACACAGGGCAGGAA[C/T]TTGGAGGCAGGAGCT | 68519 |
| rs264238340 | snp | A/C | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108413183 | GGCTCTTTATGCAGC[A/C]CTGATATTGATAGAC | 68519 |
| rs264240500 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108457088 | GAAGTCTCCTGAGTC[C/T]CTGACTCATTCCTCA | 68519 |
| rs264247099 | in-del | -/GAC | | | intron-variant | Eml1 | Mm_Celera | 12:108470329 | TCTTTAAATTTCTTT[-/GAC]AAACTTGTAAAGTTC | 68519 |
| rs264252616 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108377313 | TTGGGGACAACTGAC[A/G]CCCTCATTATCCTGC | 68519 |
| rs264264833 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108426044 | TGCATGCATCTCTGC[A/G]TATGCATGTGAAGGG | 68519 |
| rs264268025 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108387202 | AAAAGGTCACAGGTG[G/T]AAAACAGGGAAGGAG | 68519 |
| rs264269434 | in-del | -/CACACAC | | | intron-variant | Eml1 | Mm_Celera | 12:108390049 | CTTAAAAAAAAAAAA[-/CACACAC]ACACATTGTAGGAAC | 68519 |
| rs264281788 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108397251 | GTGGAGGGGGCATTC[C/T]GAATGTGAGTAACAA | 68519 |
| rs264283153 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108470870 | TGTGGACTTGTTCTC[C/T]TCTCTCTGCCCATCT | 68519 |
| rs264301286 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108446264 | AAGGTCATTAATATG[G/T]CAGGGCACACCCTCT | 68519 |
| rs264316116 | snp | G/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403552 | CTTTTTCCACCCTTG[G/T]CTACTGTGGATAGGG | 68519 |
| rs264318977 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108452358 | CAGGCCAGCTTGCAC[A/G]TGGCAGCTTGCAGGG | 68519 |
| rs264326036 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108530672 | GAACTCCTAGAGATT[-/C]CCCCTGCCTCCACCT | 68519 |
| rs264331409 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108502158 | ACCCTCTGGAGCAGC[C/T]GGCCAGCCACACTGA | 68519 |
| rs264346612 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108381133 | CTCAGGGAGAGGGCT[G/T]GGGGAGAGGGGCGGG | 68519 |
| rs264360161 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108432206 | GCAGGAAGGACAATC[C/T]AGACCTGGGAAAGCC | 68519 |
| rs264368186 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108476888 | TCCAAGCACAGGAAG[C/T]CAGGGGCAGGAACAT | 68519 |
| rs264380763 | in-del | -/CT | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108406474 | TACTCCTGCATTCCA[-/CT]CCACCCACCCCGCAC | 68519 |
| rs264380800 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108508327 | TAATAAAATTTAAAA[A/C]CATTGATAATTATCC | 68519 |
| rs264383553 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108380740 | TTTGAGATATTATTG[-/A]AAAAAAATCCTTGCC | 68519 |
| rs264384209 | in-del | -/GACTCTGC | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405052 | CTGGGCCCCACATAT[-/GACTCTGC]AAGTCTAGTCTGCCC | 68519 |
| rs264403317 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370525 | TTGACTCTTAGTCAC[A/G]CATACAGCAAGCACA | 68519 |
| rs264412232 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108483960 | GTCTATACACAGAAA[A/G]TTAAAATAAATAAAT | 68519 |
| rs264451185 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108479748 | AGCTTTGCTAACATG[C/T]AATTATTCATAGTAG | 68519 |
| rs264473893 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108482875 | AGGATTCGTTGAAAG[A/G]GATCACAGTTTTTAA | 68519 |
| rs264480851 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108533376 | CACTCCATTTCCACA[A/G]CTCCCTGGCCCTGCT | 68519 |
| rs264484823 | in-del | -/AGCTCTGAA | | | intron-variant | Eml1 | Mm_Celera | 12:108432430 | TCTGGGTAGATATTT[-/AGCTCTGAA]AGGTCGCTGTCAGTG | 68519 |
| rs264494043 | in-del | -/GGCACTGGGTGGCA | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407637 | GGTCCTAGAACCCCT[-/GGCACTGGGTGGCA]GGCACTGGGTGACAG | 68519 |
| rs264508064 | in-del | -/T | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369663 | GGGGCCCAGAACTAG[-/T]TTTTTTTTTCCTTTT | 68519 |
| rs264508253 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108516679 | CCGTTTGGATTCGCT[-/C]GGGGGGGGGGGGGGG | 68519 |
| rs264518000 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445899 | CTGAGGCAAATTGAA[A/T]TTTAAAAGCTTAGGG | 68519 |
| rs264534372 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108390492 | aaaaaaattaaaaaa[A/T]aCACATTTTCAAACA | 68519 |
| rs264539157 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403105 | AGTACATTTAAGGCA[A/G]TTCCCACCACTGATT | 68519 |
| rs264539231 | in-del | -/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405375 | GCAGAGTCTGGACCA[-/G]GGAGGTGGTGTCTGT | 68519 |
| rs264541434 | in-del | -/ACTT | | | intron-variant | Eml1 | Mm_Celera | 12:108380373 | CATCATCTCTAGGTG[-/ACTT]ACTTACACTTCCTGC | 68519 |
| rs264547529 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108499877 | TGACGAAGGTGGATC[C/T]TGTGCTTACAAGGGC | 68519 |
| rs264567891 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108501614 | ATGGACATATGGCTG[A/G]CTCCACCCCTTGCTG | 68519 |
| rs264579605 | snp | A/G | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405795 | AGGAATCAGAATGCC[A/G]TGCAGGCTAATGTCC | 68519 |
| rs264601698 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108454880 | CCTCTTGGGTGGTCC[A/G]TCCAGGGCCAGTTTC | 68519 |
| rs264630237 | in-del | -/CA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499228 | TCACTCACACACCCC[-/CA]CCCACACACACACAT | 68519 |
| rs264661225 | snp | C/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108401530 | GTCACAGGAAATGCA[C/G]GGTGTGCTGTCTGTG | 68519 |
| rs264667100 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108479928 | GTTTTAGGAAACCAA[-/C]CCCCCGGTATTGCTG | 68519 |
| rs264677835 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408176 | GTTACTCTGACTGGC[C/T]TTGAACTCAAAGATC | 68519 |
| rs264680018 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108455896 | ATGGTATGCTGAGCT[C/T]GCTCTAGGTTTGGGG | 68519 |
| rs264685426 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108505938 | TTTATTTACATGTAT[A/G]TGTCTCTGTGTGTGG | 68519 |
| rs264689841 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108432393 | GTAATCCTCCTCGTC[-/T]TTATCAATGGCCGTC | 68519 |
| rs264712861 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108430039 | TTAGTTGTCCTTTTT[-/A]AAATCTTGGATCAGC | 68519 |
| rs264735815 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108380669 | TGCTCTACAGCAGCT[C/T]GTTCATGGGACATAA | 68519 |
| rs264751490 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108462579 | CAAAGCCCACCCGCC[A/G]GTGACATACTTCCAA | 68519 |
| rs264751974 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108527482 | CCTTTTGTGATTACT[A/G]TAGATAGGACAGATT | 68519 |
| rs264757226 | in-del | -/TA | | | intron-variant | Eml1 | Mm_Celera | 12:108467268 | GTATGTCATAAATGC[-/TA]TGAGTCCTGTTGTTC | 68519 |
| rs264759047 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108437635 | TTTATCTTGTGCTGA[C/T]CACTGCAGCTAGCTG | 68519 |
| rs264759419 | in-del | -/AACTCTGG | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402064 | TGTGACTTACTGTGT[-/AACTCTGG]AGCTCTGGCCAGCAT | 68519 |
| rs264782343 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403339 | TTGATCTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 68519 |
| rs264784829 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451985 | TAAAGATTCCACACA[C/G]TCCCAAATAGTTCTA | 68519 |
| rs264798014 | snp | G/T | | | intron-variant, missense | Eml1, Gm33385 | Mm_Celera | 12:108411081 | TAGGAGGAAGAGCAG[G/T]CTCGGCAATGTGCAA | 68519 |
| rs264807148 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108458630 | CATCATTGCATATAT[A/G]ATTTGTTGTGAAATG | 68519 |
| rs264813513 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108508113 | TTAAAGTACACATGT[G/T]AAAATTTTTAACACT | 68519 |
| rs264816956 | in-del | -/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381131 | AGCTCAGGGAGAGGG[-/C]TGGGGGAGAGGGGCG | 68519 |
| rs264822667 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108516029 | GGAAACACAGACCGC[C/T]CGCCCGATGTTACTT | 68519 |
| rs264852392 | in-del | -/TAA | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403703 | CTCAATTGATAACTT[-/TAA]AAAAAAAACCACACA | 68519 |
| rs264864476 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108433214 | GACCGTGAGTGGTGG[A/G]TCTGACCGAGTCAGA | 68519 |
| rs264906526 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468882 | ggaggaggaggaaga[A/G]gaagaAGaagaagat | 68519 |
| rs264932036 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108434889 | CATATACTACATCCC[A/C]CACACTTACATACAT | 68519 |
| rs264935596 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480005 | CTCATTCACCTTCAT[C/T]GGCTCCTTTCTTCCG | 68519 |
| rs264948029 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108488607 | TGGAAACTGTAACTT[-/A]GACTTCCAGCCCACA | 68519 |
| rs264959004 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108486868 | ACCACACCTGATTGG[A/G]ATTCTCAAATATTGG | 68519 |
| rs264993867 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381103 | TCGGGGCGGGGTTCG[A/G]GGTTCAGGGCGGAGC | 68519 |
| rs265021370 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108438220 | TTCACAGGTCACACA[C/T]ACCTGGCAAGAAATA | 68519 |
| rs265029480 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108483944 | ATACCCACAAGCAAA[C/T]GTCTATACACAGAAA | 68519 |
| rs265036725 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108534059 | GATATGGGAAAGCCT[C/G]TAGCATCCTGGCTCT | 68519 |
| rs265038185 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443641 | GGCCCTGGGGCATAA[A/G]CGATGAGCACTGCCA | 68519 |
| rs265038756 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108491873 | ATGCTATGATGTACC[C/T]GGTACACTAATCCAC | 68519 |
| rs265082597 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108478245 | ATGTTCATGCCTGTG[A/G]CAAACAACACGCGTT | 68519 |
| rs265084700 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108451552 | GGAAACCTTTGGGGG[A/T]GGTTCAGATGTGCTC | 68519 |
| rs265094802 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108485165 | TGAGGAGCAGACCAA[A/G]GAGGAAAAGATGGGT | 68519 |
| rs265112533 | in-del | -/AAG | | | intron-variant | Eml1 | Mm_Celera | 12:108415386 | AAAAAAAAAAAAAAA[-/AAG]AAGAAGACCTACTTT | 68519 |
| rs265150262 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108408966 | AATTCAAAGGCAGTC[A/G]TACCGTGTTTTGTTG | 68519 |
| rs265152194 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456996 | CTCCTGCTTCCTCTC[A/G]GGAATTGTCCAACCC | 68519 |
| rs265166611 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108416476 | CCAGAGGCTCTGCTA[A/G]CAGGCTTATGGGGAA | 68519 |
| rs265176044 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108462946 | AAGCTCTGAGGGCCA[C/T]GTCTGGTGTTGCTAT | 68519 |
| rs265181168 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108514292 | GTCGGTGGGGCTTGA[A/G]AGACTCAGTGCCCCA | 68519 |
| rs265188353 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108489612 | TTCAATTCCCAGAAC[C/T]TGTATGGCAGCTCTC | 68519 |
| rs265214541 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108441913 | TTGGCATTTTAGAGC[C/T]CAGTAGCTTAGGGAA | 68519 |
| rs265228317 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460508 | TCATAAGAACACCAG[A/G]GGCAGGAAAATTGGG | 68519 |
| rs265229984 | snp | C/T | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108538364 | GGAGCCAGTGCGTGT[C/T]ACACCAGATAAGCGG | 68519 |
| rs265232024 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108495901 | TTTCTGCTCAGTGGA[A/G]AAACAAAATAAAACA | 68519 |
| rs265249415 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460351 | AAAAACTTCAAAAAT[A/G]GAAGCATCCCTGGTC | 68519 |
| rs265270406 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108412079 | GATGGTGCAATCCGA[C/T]TGGGACCAGTCTCTA | 68519 |
| rs265286797 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108419110 | ATTTCTGCTCCATCT[C/T]CGATCCTGACTACTC | 68519 |
| rs265307648 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108415006 | CTCAGCCTTTCCACG[A/C]TAGCTGGAATGACTA | 68519 |
| rs265322863 | in-del | -/CT | | | intron-variant | Eml1 | Mm_Celera | 12:108530578 | GCCCGCTGTCTAGTC[-/CT]CTCTCTGTTTTTCCA | 68519 |
| rs265323831 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108512505 | ACCAGCTAGGCTCTT[C/T]ACCTAGCTCTGTAAT | 68519 |
| rs265328256 | in-del | -/C | | | intron-variant, downstream-variant-500B | Eml1, Gm33385 | Mm_Celera | 12:108400472 | GTGAACCACACACAG[-/C]CATCACCTAGGATCT | 68519 |
| rs265338141 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468387 | TGAGTACACCAAGAA[A/G]TCTGGTTTTGAAAAA | 68519 |
| rs265347794 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108519526 | GGGACCGCATCTCAC[C/T]AAGGCATGGAGCTTG | 68519 |
| rs265352230 | in-del | -/ATGC | | | intron-variant | Eml1 | Mm_Celera | 12:108441649 | AGCCCACAGCTCCAG[-/ATGC]AGGCTGATTGTCACT | 68519 |
| rs265371707 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108385866 | GCACATCGGGAGGGC[A/C]CATCCCCAACAGCAC | 68519 |
| rs265374382 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108466918 | TGCAGATGCCCCAAA[A/G]GCCATAGAAGGATGT | 68519 |
| rs265374746 | in-del | -/TAGA | | | intron-variant | Eml1 | Mm_Celera | 12:108461100 | AGGTAGATAGATAGG[-/TAGA]TAGATAGATAGATCA | 68519 |
| rs265380166 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108518287 | ATTCAGATATATATG[A/G]ATATATACACTTTTA | 68519 |
| rs265382661 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108437020 | GCGTTCTGTCTAGAA[C/T]GTTCTCTGGAACTGA | 68519 |
| rs265387486 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108392657 | CAAATGAAGCCCAGT[A/G]TATAAGAGGTGCTTC | 68519 |
| rs265400223 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442514 | TCTTTACACTGGAAC[A/G]TTTGATTTAAAACAA | 68519 |
| rs265430146 | snp | C/T | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108369691 | TTTGAGGTTCAGTGG[C/T]CCTCAGTATCAGTAT | 68519 |
| rs265431806 | in-del | -/GTAC | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457501 | TGTGTGTGTGTGTGT[-/GTAC]AGCATCTCCATCACA | 68519 |
| rs265435273 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108417370 | TAGCTAACATGGTAT[G/T]GCCGGGTATCGTAGA | 68519 |
| rs265457620 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108471058 | GAACCATATCTTAAG[C/T]AGCAAAAGCATCGTT | 68519 |
| rs265465960 | in-del | -/ATTTATGC | | | intron-variant | Eml1 | Mm_Celera | 12:108494918 | ACCTGCATGGACATG[-/ATTTATGC]TATGCGAGCCAAAGG | 68519 |
| rs265466711 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522005 | GGACCAGTGGGACCC[A/G]GGCACCCAGGAACTC | 68519 |
| rs265471785 | in-del | -/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454453 | CTTTCCCTCCCTCCC[-/T]TCCCTCCCTCCCTCC | 68519 |
| rs265510605 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108465048 | TTTGTTTCTTTGAGA[C/T]AGGGTTTCTCTGTGT | 68519 |
| rs265542813 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108524585 | AAGAAAGTGGAAGAG[C/T]GTACACTAGCCGCTT | 68519 |
| rs265548752 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441650 | GCCCACAGCTCCAGA[G/T]GCAGGCTGATTGTCA | 68519 |
| rs265556981 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108450723 | CTGGGGTAGGACACG[A/G]AGTCTAAAGCTGGGC | 68519 |
| rs265577062 | snp | A/C | | | intron-variant | Eml1 | Mm_Celera | 12:108486198 | CAGACCTGACTAATG[A/C]GCTAAGACCCCAAGG | 68519 |
| rs265598052 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418392 | GATGCAGAGGCTATG[A/G]AGGGATGTTCTTTAC | 68519 |
| rs265600375 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108493827 | TTGATTCACCTTCGC[A/G]GGACTTGTTGACAGC | 68519 |
| rs265613225 | in-del | -/C | | | intron-variant | Eml1 | Mm_Celera | 12:108376336 | CGTCACCCTTCTCCT[-/C]CCCCGCCTTTTTTTT | 68519 |
| rs265624518 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108528295 | TCCGCTTTTGAAATG[A/G]GCAAGAAAGCATTGC | 68519 |
| rs265652350 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108393393 | AAGGAACAGACTCTA[C/G]AGTGCCACTGACCTG | 68519 |
| rs265659411 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108443109 | AATTTGAGGCCAGCC[C/G]GGTCTACACCGAAAG | 68519 |
| rs265712511 | in-del | -/TGTGTGTGTGTGTGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108486683 | TATGGGATTCCCATA[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 68519 |
| rs265725854 | snp | A/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429058 | CATTTATTTCTCCTG[A/T]AAGAATTAACAGTGA | 68519 |
| rs265734528 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108492517 | CTTCTCTTTTAGAGT[C/T]GCTTTATTTCACAAG | 68519 |
| rs265754903 | in-del | -/TCGTTTTTTTGTTGTTG | | | intron-variant | Eml1 | Mm_Celera | 12:108449095 | ATGCATACATTGGTT[-/TCGTTTTTTTGTTGTTG]TTGTTTTTTTAAAGA | 68519 |
| rs265756176 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108396052 | GGTGGGGGTGGGGGG[A/G]AAGGAAGGCTCATTC | 68519 |
| rs265786051 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108415841 | GAAATTCATAGGAAT[A/G]CAGAAGCCACCTTCC | 68519 |
| rs265803564 | snp | A/G | | | utr-variant-5-prime, intron-variant | Eml1 | GRCm38.p3 | 12:108423134 | CGCCAGCGCCGCGGC[A/G]GCTCGGCAGGGCGCA | 68519 |
| rs265807905 | snp | C/G | | | intron-variant | Eml1 | Mm_Celera | 12:108469252 | GGGCCACATTGTGTC[C/G]CCAATCAGGAAGCAG | 68519 |
| rs265823409 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108520195 | AGCAGCCAGAACTGC[C/T]CTTGACAGAAGTGTT | 68519 |
| rs265862875 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494892 | TGTGTGTGCGTGCAC[A/G]CGCGCACGCTCACCT | 68519 |
| rs265867110 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108432743 | CCAAAGGATCTGGAG[C/T]CTCAAGGTGCCAGGA | 68519 |
| rs265870952 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452755 | CAGCTGGGAGCTGGC[A/T]GTGTAAGCCAGGCTG | 68519 |
| rs265873119 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108502457 | ATTGGGGGAGGGGGC[A/G]TATAATTTAGACCTT | 68519 |
| rs265901737 | snp | A/G | | | upstream-variant-2KB | Eml1 | Mm_Celera | 12:108370996 | AGGAAAAGGCATTCC[A/G]TAGTCTCCAGAGCTG | 68519 |
| rs265918042 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377955 | GTGTGCGCGCGCGCG[C/T]GCGTGTGCGTGTGCA | 68519 |
| rs265925684 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108427830 | TGAGTTCAAGGTCAG[A/C]CTAGTCTACATAGTG | 68519 |
| rs265950049 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108503829 | CGTTAGTCTTAGCAC[C/T]CTGGCTGGGTTGATC | 68519 |
| rs265957390 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467361 | CCCGGGCATTGAACC[C/T]GTAGACATGGAGGGC | 68519 |
| rs265995576 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108429245 | CTCTCCTTCCACTGT[G/T]TGGGTTCAGGGAACT | 68519 |
| rs265999792 | snp | A/C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473808 | ATCACCTCCCAGCTT[A/C/G]GTTTCCTGCTGCTGT | 68519 |
| rs266007113 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108391477 | GCTGTGCGTAGGCCT[A/G]CATCTGCCTTTCTCC | 68519 |
| rs266015656 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108525673 | AAGTCTAAATGTAGC[C/T]GTGCGTGGTGGCACA | 68519 |
| rs266037800 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108385747 | AGGTCGTCCTTGCTA[A/C]ATATGACATTTGAGA | 68519 |
| rs266062046 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108376558 | TCTGTATTCTCTCAT[C/T]CATCACATCCTGATG | 68519 |
| rs266069953 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108424799 | CTTGCCTTCTATCAA[C/T]TGCCAGTTTAGAGAT | 68519 |
| rs266072785 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108470484 | TGAATGCCTGGTGCC[C/T]AAGGAGGTCAGAGGA | 68519 |
| rs266078926 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381660 | AAGATTTGGTTCCAG[G/T]ACCAGCAAGAAGCAA | 68519 |
| rs266092112 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108505782 | GTCACAGGAAATGAC[-/TG]TTGGAATCTCACTCA | 68519 |
| rs266097925 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108477727 | TCTCCGTTTCCTTTC[A/G]GATCGGGAGGGAATA | 68519 |
| rs266142589 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108520555 | CACTCCTCCCCAAAC[-/T]TTTTTTTTTTCTTGT | 68519 |
| rs266151445 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108471719 | TCCCACCACTTGCCT[C/T]TGTACCCCTGCCACT | 68519 |
| rs266155160 | snp | A/G | | | intron-variant | Eml1 | Mm_Celera | 12:108524117 | TGATTGTATAGCCGG[A/G]TGGTGGTGGCACACA | 68519 |
| rs266161626 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478880 | ATCTTTTCCCACTCT[C/T]GGAGAGAACGCTTAC | 68519 |
| rs266198636 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108509612 | TTTATAAAGTTTAAG[-/A]AAAAAAGTTTAGGCC | 68519 |
| rs266204523 | snp | G/T | | | intron-variant | Eml1 | Mm_Celera | 12:108395445 | TGCTGGAGTGGGGGA[G/T]GGGGAGTGGATGCAG | 68519 |
| rs266209507 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108445262 | TTGCAGAGAAAATGT[C/T]TCCAAGTATAGAGTT | 68519 |
| rs266219446 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108392686 | TCATCAAACCCCTGC[A/G]TCCCCTGGGCCAGCA | 68519 |
| rs266251222 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377577 | CACGAGGACTTCCTG[C/T]TTACGGGAAGAATCC | 68519 |
| rs386834774 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489456 | AGAGGAGGAGGAGGA[A/G]GAGGAGGAGGAGGAG | 68519 |
| rs386837345 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108380747 | TATTATTGAAAAAAA[-/A]TCCTTGCCCAGAATG | 68519 |
| rs386843132 | in-del | -/TTTAAAAGCC | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411508 | AAACCTTTAAAAACC[-/TTTAAAAGCC]CCACTGGGATAGTGG | 68519 |
| rs386848950 | in-del | -/TGTGTG | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | Mm_Celera | 12:108535910 | GTGTGTGTGTGTGTG[-/TGTGTG]CTTGTCTGTCTGTCT | 68519 |
| rs386870770 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108432395 | AATCCTCCTCGTCTT[-/T]ATCAATGGCCGTCAC | 68519 |
| rs386875166 | in-del | -/TGTGTGTGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108494875 | GTGTGTGTGTGTGTG[-/TGTGTGTGTG]CGTGCACACGCGCAC | 68519 |
| rs386888106 | in-del | -/TC | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108407476 | GAGACAGAGATAGAG[-/TC]AGAGTCAAATAAGAT | 68519 |
| rs386889232 | in-del | -/T | | | utr-variant-5-prime, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108410647 | AGATACACAAGGTCT[-/T]GTGGCAGAAAGCAGG | 68519 |
| rs386930357 | in-del | -/TTTTTTTTTTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108432036 | CATCTTTTTTTTTTT[-/TTTTTTTTTTTT]CAGTTACTTAGTGAC | 68519 |
| rs386938514 | snp | C/T | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402943 | CTCTCTCTCTCTCTC[C/T]CTCTCTCTCTCATGG | 68519 |
| rs386953345 | snp | A/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402032 | TTGTGTGTGTGTGTG[A/T]GTGTGTGTGTGTGTG | 68519 |
| rs386956153 | in-del | -/TGTGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108517410 | GTGTGTGTGTGTGTG[-/TGTGTG]CCTGTGCACACTCAT | 68519 |
| rs386958715 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108415589 | AATCTTAAAAAAAAA[-/A]GAAAACCAGCTGCAA | 68519 |
| rs386961860 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381087 | GGGAGTGGGGCCGGG[C/T]TCGGGGCGGGGTTCG | 68519 |
| rs386977725 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108420150 | TGCTTTTTTTTTTTA[-/A]CCCAAATTTTATAAT | 68519 |
| rs386978545 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108382017 | CCATCTCTGCCTGGG[-/G]AGGCTGGCCCAGAAA | 68519 |
| rs386990558 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108433448 | ACATAACAAGAATTT[-/T]AACACTCCTAAGGAA | 68519 |
| rs386992369 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108439881 | TCTTAAAAAAAAAAA[-/A]GAAAAAAAAATTCCA | 68519 |
| rs387019031 | in-del | -/GC | | | intron-variant | Eml1 | Mm_Celera | 12:108387651 | AACAAATCCTTCTCC[-/GC]CCCCTCCAGCTGCTT | 68519 |
| rs387022921 | in-del | -/CA | | | intron-variant | Eml1 | Mm_Celera | 12:108434637 | ACACACGCACACACA[-/CA]TCATTTACCACACAC | 68519 |
| rs387030855 | in-del | -/CTCG | | | intron-variant | Eml1 | Mm_Celera | 12:108507277 | CTGTGCTAACTCCAG[-/CTCG]TGTCAAGTTGCCACA | 68519 |
| rs387041428 | in-del | -/CACACACA | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409671 | TCTCTCTGCCACACT[-/CACACACA]CACACACACACACAC | 68519 |
| rs387046652 | in-del | -/GGTGG | | | intron-variant | Eml1 | Mm_Celera | 12:108397235 | TTCTATTGGGTTGGG[-/GGTGG]AGGGGGCATTCCGAA | 68519 |
| rs387073336 | in-del | -/AACT | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402889 | TCCATCTAACCATCT[-/AACT]CTTTCCCAGAATATT | 68519 |
| rs387081888 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108471419 | GAGGAGGAGCAGGGG[-/G]GGAAGAGCAGGGGAG | 68519 |
| rs387101131 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108379444 | TCTCTCTGGTCTCTT[-/TT]CTCATTGATCCCAGC | 68519 |
| rs387106647 | in-del | -/AGACAGAC | | | intron-variant | Eml1 | Mm_Celera | 12:108391019 | AAACACTACATAGAC[-/AGACAGAC]TGATAGGCACATACA | 68519 |
| rs387112858 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108532223 | GGTCTTTTTTTTTTT[-/T]AAGATTTATTTTTAT | 68519 |
| rs387117890 | in-del | -/AA | | | intron-variant | Eml1 | Mm_Celera | 12:108499921 | GAAGGGAGGGGGGAA[-/AA]TCAAACATTCACAGA | 68519 |
| rs387123724 | in-del | -/AA | | | intron-variant | Eml1 | Mm_Celera | 12:108429729 | GAGTGGGGGAAAAAA[-/AA]CCCTAAATTGTGTTT | 68519 |
| rs387129242 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108429145 | TGTGTGTGTGCGCGC[G/T]CGCATGCGTGCGCGC | 68519 |
| rs387162177 | in-del | -/AAG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468633 | AAGAAGAAGAAGAAG[-/AAG]GAAGAAAGAAGAAGG | 68519 |
| rs387179957 | in-del | -/G | | | intron-variant, frameshift-variant | Eml1, Gm33385 | Mm_Celera | 12:108411060 | CGTGGCTCCAGGGGG[-/G]CAGGATAGGAGGAAG | 68519 |
| rs387182737 | in-del | -/GGT | | | intron-variant | Eml1 | Mm_Celera | 12:108378652 | AGTAGTAGTAGTAGT[-/GGT]AGTAGTAGTAATTAT | 68519 |
| rs387187396 | in-del | -/A | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405816 | GCTAATGTCCTCTGA[-/A]TTGCTCTGAAGTTGG | 68519 |
| rs387195626 | in-del | -/ACCCA | | | intron-variant | Eml1 | Mm_Celera | 12:108432161 | TGGCTGATCTTTCCA[-/ACCCA]CTCACTGCCCGCCAG | 68519 |
| rs387197069 | in-del | -/TGTGTGTGTG | | | intron-variant | Eml1 | Mm_Celera | 12:108479097 | GTGTGTGTGTGTGTG[-/TGTGTGTGTG]AGTGTGCCACAGCAT | 68519 |
| rs387213040 | in-del | -/GTTTGTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108428886 | TTTGTTTGTTTGTTT[-/GTTTGTTT]TAAGGTCCCACTATT | 68519 |
| rs387233420 | in-del | -/CTT | | | intron-variant | Eml1 | Mm_Celera | 12:108529378 | CCACCATCCATAACT[-/CTT]GTCTTTCTGGGAGAT | 68519 |
| rs387237227 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468873 | GGAGGAGGAGGAGGA[A/G]GAGGAAGAGGAAGAA | 68519 |
| rs387246727 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108497830 | AACTAATTTTATGGG[-/G]TGGGGGAAATCACCA | 68519 |
| rs387255970 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457489 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGT]ACAGCATCTCCATCA | 68519 |
| rs387257995 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108416144 | TGGAAAGAGAGAGAG[-/AG]GGTCGTCATCCCCCT | 68519 |
| rs387279515 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108383540 | ACATTCTATTTTTTT[-/T]AAGATTTATTTATTT | 68519 |
| rs387290707 | in-del | -/CTCTGAAAG | | | intron-variant | Eml1 | Mm_Celera | 12:108432432 | TGGGTAGATATTTAG[-/CTCTGAAAG]GTCGCTGTCAGTGGT | 68519 |
| rs387298859 | in-del | -/GT | | | intron-variant | Eml1 | Mm_Celera | 12:108486720 | TGTGTGTGTGTGTGT[-/GT]ACATATATGCATATC | 68519 |
| rs387302556 | in-del | -/AGAGAGAGAG | | | intron-variant | Eml1 | Mm_Celera | 12:108499957 | GAGAGAGAGAGAGAG[-/AGAGAGAGAG]TATGGTTGGAGCAAG | 68519 |
| rs387303453 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108388479 | CAGCTTCCCTGGGGG[-/G]CTATGGCCAGGGACC | 68519 |
| rs387318074 | in-del | -/CTCT | | | intron-variant | Eml1 | Mm_Celera | 12:108433517 | TCTCTCTCTCTCTCT[-/CTCT]TTCATGCTATATAGG | 68519 |
| rs387336967 | in-del | -/TG | | | intron-variant | Eml1 | Mm_Celera | 12:108377429 | AGCCACAAATAACTG[-/TG]CGTGCGTGTGCCCTC | 68519 |
| rs387351574 | in-del | -/ACACACACACAC | | | intron-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108537735 | CACACACACACACAC[-/ACACACACACAC]TCTCTGCCTACCTAC | 68519 |
| rs387353198 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108381027 | AGGGGCGGGGAGCAG[-/G]TAACAGGGAGAGAGG | 68519 |
| rs387362950 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108420432 | TCTTTGAGATTTTTT[-/T]CTTTCTTTTTCCTTC | 68519 |
| rs387371426 | in-del | -/AC | | | intron-variant | Eml1 | Mm_Celera | 12:108451373 | CACACACACACACAC[-/AC]CACACCTATAGCAGA | 68519 |
| rs387376237 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108399910 | GTAAGTTAGGCACTG[-/G]CTCACAAGAGTGTCC | 68519 |
| rs387388043 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108429122 | TTCTATTTACGTGGT[-/AT]GTGTGTGTGTGTGTG | 68519 |
| rs387420517 | in-del | -/CACAGACAGACAGACA | | | intron-variant | Eml1 | Mm_Celera | 12:108391063 | AGAAAGAGACACACA[-/CACAGACAGACAGACA]GACAGACAGACAGAC | 68519 |
| rs387422173 | in-del | -/GAA | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412620 | CTGGGATGGCAAGAA[-/GAA]TTATGGATGAAATGC | 68519 |
| rs387449721 | in-del | -/TACATAA | | | intron-variant | Eml1 | Mm_Celera | 12:108434766 | TGTACTACACACACA[-/TACATAA]CACATACCTCATATC | 68519 |
| rs387487066 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108507449 | ACCCTGTCTCAAAAA[-/A]CCAAAACCAGCCAGT | 68519 |
| rs387487475 | snp | C/T | | | intron-variant | Eml1 | Mm_Celera | 12:108414421 | ACACACACACACACA[C/T]ACACACACACACACA | 68519 |
| rs387494097 | in-del | -/GT | | | intron-variant | Eml1 | Mm_Celera | 12:108425843 | GGTGTGTGTGTGTGT[-/GT]CTGTGGTGTGTGGGG | 68519 |
| rs387495555 | in-del | -/NTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108379168 | TGCGTGTGCGTGTGT[-/NTGTGT]GTGTGTGTGTGTGTG | 68519 |
| rs387499795 | in-del | -/TC | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108409873 | CTGTGTCTCTCTGTC[-/TC]ACACACACACACACA | 68519 |
| rs387509333 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108483578 | TTTATTTTTTTTTTT[-/T]CTTCTTCTACAAATA | 68519 |
| rs387516110 | in-del | -/CAGGGTGCCAGAA | | | utr-variant-3-prime, intron-variant | Eml1, Gm16596 | Mm_Celera | 12:108539484 | CCTGCTGTGGAAGGA[-/CAGGGTGCCAGAA]AACAACGTGACTCAA | 68519 |
| rs387528343 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402075 | TGTGTAGCTCTGGCC[A/G]GCATTAAACTCATGG | 68519 |
| rs387549271 | in-del | -/CAGACAGA | | | intron-variant | Eml1 | Mm_Celera | 12:108459745 | AGACAGACAGACAGA[-/CAGACAGA]TAGATATAGGATGAA | 68519 |
| rs387557607 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108420010 | TTGGGCACAAAAAAA[-/A]TCACACATTATCAAT | 68519 |
| rs387563374 | in-del | -/CTTT | | | intron-variant | Eml1 | Mm_Celera | 12:108379653 | TGAGTTTCTTTCTTT[-/CTTT]GATCCTATCCTTTAT | 68519 |
| rs387563946 | in-del | -/CT | | | intron-variant | Eml1 | GRCm38.p3 | 12:108530584 | TGTCTAGTCCTCTCT[-/CT]GTTTTTCCAGACAGG | 68519 |
| rs387568701 | in-del | -/TTTTGTTTTTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108439265 | TGTTTTTGTTTTTGT[-/TTTTGTTTTTGT]GTAGAGCTGACTGTG | 68519 |
| rs387574146 | in-del | -/ACAAA | | | intron-variant | Eml1 | Mm_Celera | 12:108525837 | ACAAAACAAAACAAA[-/ACAAA]CAAAAAAAGAAGTCT | 68519 |
| rs387591100 | in-del | -/G | | | intron-variant | Eml1 | Mm_Celera | 12:108385504 | TGCAGGTTCTGTGGG[-/G]TAAGTCCTGGGTTCT | 68519 |
| rs387608625 | in-del | -/TT | | | intron-variant | Eml1 | Mm_Celera | 12:108502373 | AAATACTTTTTTTTT[-/TT]GGTTTATTTTCACAG | 68519 |
| rs387611411 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108381484 | ACCAGAACAGAGACA[-/A]CGTAGAGAGCCCAGG | 68519 |
| rs387614314 | in-del | -/GGA | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468696 | GGAGGAGGAGGAGGA[-/GGA]AAGAAGAAGAAGGAA | 68519 |
| rs387623252 | in-del | -/A | | | intron-variant | Eml1 | Mm_Celera | 12:108493973 | TGATTTAAAAAAAAA[-/A]TGGCGCTCAAATCAT | 68519 |
| rs387624807 | in-del | -/GT | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | Mm_Celera | 12:108411215 | CCTTCATCGCTGTCT[-/GT]ATTCCTCACCAGGTG | 68519 |
| rs387627001 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108490145 | ATATTTACAAAGGGA[-/T]TTTTTTTTTTTTTTG | 68519 |
| rs387629408 | in-del | -/CT | | | intron-variant | Eml1 | Mm_Celera | 12:108432874 | GCAACTCCTCTCTCT[-/CT]GTCTCTTTGGCATCC | 68519 |
| rs387634953 | in-del | -/AG | | | intron-variant | Eml1 | Mm_Celera | 12:108498729 | GCACCATAAAGAAAG[-/AG]TGTTGGATCCTGGGA | 68519 |
| rs387642659 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402012 | CTGTGGTTCTGTGGC[A/G]TGTTTTGTGTGTGTG | 68519 |
| rs387645400 | in-del | -/GTGTGTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108475768 | TGTGTGTGTGTGTGT[-/GTGTGTGTGT]ATCTTGTCATGGCCT | 68519 |
| rs387656350 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108429141 | TGTGTGTGTGTGTGC[A/G]CGCGCGCATGCGTGC | 68519 |
| rs387657439 | in-del | -/TACA | | | intron-variant | Eml1 | Mm_Celera | 12:108432250 | AGTGAAGAGTAGAGA[-/TACA]GGAGGATGGAGTGAG | 68519 |
| rs387675434 | in-del | -/A | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108403065 | GCCCCAGCTATCTCA[-/A]CCACGTCTCAGTGGA | 68519 |
| rs387677735 | in-del | -/CT | | | intron-variant | Eml1 | Mm_Celera | 12:108429182 | TGAGTGTTTGTGCCT[-/CT]GCCTTGCATGTGGAT | 68519 |
| rs387692028 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108497663 | TAGCAATGTATCTGC[-/T]TTTTTTTTTCTTTTT | 68519 |
| rs387739323 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108431611 | ACAGGTGCACACATT[-/T]AACACGCTTATGCAC | 68519 |
| rs387740950 | in-del | -/CG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377957 | GTGCGCGCGCGCGCG[-/CG]TGTGCGTGTGCATGC | 68519 |
| rs387757234 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108389737 | AAGCTGAGCCCCCTT[-/T]AGTAAAACGACTAAG | 68519 |
| rs387780568 | in-del | -/AT | | | intron-variant | Eml1 | Mm_Celera | 12:108395056 | GAAAAAAATATATAT[-/AT]CAGAGTTGAATCACG | 68519 |
| rs387796616 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108529316 | AGAGGACCCAGGTTT[-/T]GTCCCCTCCCGTCCC | 68519 |
| rs387810019 | in-del | -/GTGTGTGT | | | intron-variant | Eml1 | Mm_Celera | 12:108433987 | TGTGTGTGTGTGTGT[-/GTGTGTGT]AGGTTTAGCAGAGCA | 68519 |
| rs387812075 | in-del | -/GT | | | intron-variant | Eml1 | Mm_Celera | 12:108452944 | TGTGTGTGTGTGTGT[-/GT]ATGTGTATGTGTGTG | 68519 |
| rs387829209 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108420557 | TGTTGAGACAGGGTT[-/T]CTCTGTGTAGCCCTG | 68519 |
| rs387829376 | in-del | -/AGG | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | Mm_Celera | 12:108412742 | AGATCTCTGAGTTCG[-/AGG]TCAGCCTGATCTACA | 68519 |
| rs387847794 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108516065 | GGGAAGGGGTTTTTT[-/T]GTATTCCTCCTCATC | 68519 |
| rs387856628 | in-del | -/CACACACACACA | | | intron-variant | Eml1 | Mm_Celera | 12:108462298 | ACACACACACACACA[-/CACACACACACA]ATTTCTTAAAGCTCT | 68519 |
| rs387876789 | in-del | -/TGCAAACTGAGCCACATCCTC | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108402589 | AGGAGGCGAGCACTC[-/TGCAAACTGAGCCACATCCTC]GGCTGTTATTAGTTT | 68519 |
| rs387878978 | in-del | -/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108483567 | AAAGGAAATGTTTTA[-/T]TTTTTTTTTTTCTTC | 68519 |
| rs387886449 | in-del | -/TG | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379289 | GTGTGTGTGTGTGTG[-/TG]GCCACCGGTGCTTGA | 68519 |
| rs387893065 | in-del | -/T | | | intron-variant | Eml1 | Mm_Celera | 12:108426496 | ACCATTATTTTATTT[-/T]ATTTATTTATTTATT | 68519 |
| rs387897805 | in-del | -/AG | | | intron-variant | Eml1, Gm33385 | Mm_Celera | 12:108405364 | TCAAAAGGCTTGCAG[-/AG]TCTGGACCAGGGAGG | 68519 |
| rs387902385 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108429143 | TGTGTGTGTGTGCGC[A/G]CGCGCATGCGTGCGC | 68519 |
| rs578277540 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108526648 | CAGCCACCCAGCTCA[C/G]GCTGACTCCCAAGCC | 68519 |
| rs578281513 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518034 | CTCAAAATAAATAAA[C/T]AAATAAATAAAACAA | 68519 |
| rs578282467 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523578 | TAACAGACTGGATAC[A/G]TAGACAGGACCCAGC | 68519 |
| rs578293966 | snp | G/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108536711 | GATGTTATACCCACA[G/T]GAACACATGACACTT | 68519 |
| rs578294745 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485339 | CTATGTTCTTTGAAG[A/C]CACACACACACACAC | 68519 |
| rs578297465 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471164 | CTGTGAGAGCTGACA[C/T]AGAGGTGCATATCCA | 68519 |
| rs578302888 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523389 | ATGGATAATAGATGG[A/G]AAACACCAACACAAG | 68519 |
| rs578345656 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403280 | CAGGGTTTCTCTGTG[C/T]AGCCCTGGCTGTCCT | 68519 |
| rs578350057 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108434702 | ACACACACACATACA[C/T]ACACACACATACCAC | 68519 |
| rs578354156 | snp | A/G | | | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108421224 | TGCTGCAGGTCCCCT[A/G]GAGGCCTCTGCCACC | 68519 |
| rs578368395 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108491992 | ACCGGAGAAAGTGTC[C/T]CCATTCTGGCCTCCG | 68519 |
| rs578382319 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473244 | CACCACACACACCAA[G/T]CATAGACACACACAC | 68519 |
| rs578385859 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461024 | ACATATATAGATAGA[C/T]AGACAGACAGGTAGA | 68519 |
| rs578388804 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452930 | TTTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 68519 |
| rs578485367 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471526 | AAGGGAGGAGGAGCA[G/T]GGGAGGAGGAGGAGC | 68519 |
| rs578485409 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523958 | GACATATCATGGAAA[C/T]ACAAACTAAACAGAG | 68519 |
| rs578486231 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108503809 | CGGAAATGCCATTGT[A/T]TGGGCGTTAGTCTTA | 68519 |
| rs578487638 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456736 | TCTGTATAGCCCTGG[C/G]TGTCCTGGAACTCAC | 68519 |
| rs578507785 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108391063 | AGAAAGAGACACACA[C/G]ACAGACAGACAGACA | 68519 |
| rs578510585 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108487817 | TCTACTTCTGGACTT[C/T]GGTAGCCCCTGTTGA | 68519 |
| rs578513460 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442176 | CCAAACGTGGGGAAA[A/T]GGTAAAAATGGGCAG | 68519 |
| rs578531111 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465109 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCTGC | 68519 |
| rs578546205 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522782 | ACAAGAGATAGAAGA[A/G]AGAATCTCAGGTACA | 68519 |
| rs578573693 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108531673 | AAACAAAAAACAAAA[A/G]CAAAGACAAAAGGTG | 68519 |
| rs578574636 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376291 | CTCCTCCTCCGCTTC[C/T]TCCTTCTCCTCCTCT | 68519 |
| rs578604761 | snp | G/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407394 | ATATAGAGAGGCATA[G/T]AGAAAGAGATAGAGA | 68519 |
| rs578707541 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108448157 | TGTGTGTGTGTATGT[C/G]TGTCTGTCTGTCTGT | 68519 |
| rs578732802 | snp | A/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108536923 | AGCTGGTGTGTACTC[A/G]GGCCTCTAATATACA | 68519 |
| rs578741798 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523577 | CTAACAGACTGGATA[C/T]ATAGACAGGACCCAG | 68519 |
| rs578752177 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494850 | TATAGGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 68519 |
| rs578753629 | snp | A/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403703 | CTCAATTGATAACTT[A/T]AAAAAAAAAACCACA | 68519 |
| rs578754127 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473970 | AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGGGAGA | 68519 |
| rs578757525 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108420442 | TTTTTTCTTTCTTTT[C/T]CCTTCCTTCCTTCCT | 68519 |
| rs578761935 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461084 | GGTAGATGATAGAGA[C/T]AGGTAGATAGATAGG | 68519 |
| rs578772253 | snp | A/G | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108369330 | GGGGAGGATGGGGAG[A/G]AGGAGGGGGAAGAAG | 68519 |
| rs578793348 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108436413 | CTTTGCCCGGCCTAC[A/G]CAAGTCTGCAGTTTC | 68519 |
| rs578857932 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108503815 | TGCCATTGTATGGGC[A/G]TTAGTCTTAGCACCC | 68519 |
| rs578893393 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108524208 | GGTCTACAGAGTGAG[C/T]TCCAGGACAGCCAGG | 68519 |
| rs578936944 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108429123 | TTCTATTTACGTGGT[A/G]TGTGTGTGTGTGTGT | 68519 |
| rs578941426 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376407 | CTGTCTTCAGACACA[C/T]CAGAAGAGGGCATCA | 68519 |
| rs578943516 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465123 | CGAACTCAGAAATCT[A/G]CCTGCCTCTGCCTCC | 68519 |
| rs578949705 | snp | C/G | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408721 | TGGCCACGCCACCCC[C/G]AGAAGATGGTGCTTT | 68519 |
| rs578985782 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478367 | AATGTTTAAAGATTT[A/C]TTTATTCTTTATTCT | 68519 |
| rs578997196 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442239 | AAATGTCAAATTCAT[A/G]ATGAATCCAGGGTGT | 68519 |
| rs579019092 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108390483 | AATAATAATAAAAAA[A/T]TTAAAAAATACACAT | 68519 |
| rs579047756 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474338 | GAGAAACCCTGTCTC[A/G]AAAAACAAAAACAAA | 68519 |
| rs579082982 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108526245 | GTGAATGCATCGTAC[A/T]ATACACACACACACA | 68519 |
| rs579086932 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517931 | GGCAAAGGCAGAGGC[A/G]GAGGCAGGAGGATCT | 68519 |
| rs579099079 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484527 | AGCGTTTGCCATAGC[A/G]GGATAATAGATGCTC | 68519 |
| rs579102204 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523593 | ATAGACAGGACCCAG[A/C/T]ATTTTGCTGCATACA | 68519 |
| rs579105580 | snp | A/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471146 | TTTGATCCGCACGCA[A/G/T]TGCTGTGAGAGCTGA | 68519 |
| rs579109996 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451374 | ACACACACACACACA[C/G]CACACCTATAGCAGA | 68519 |
| rs579125191 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108420489 | TCCTTCCTTCCCTCC[C/T]TCCCTCCTTCCTTCC | 68519 |
| rs579157684 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108495500 | GCAAGAAAAGGGAAA[A/G]GGGGGCAGGCCCCCC | 68519 |
| rs579301840 | snp | A/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108409874 | CTGTGTCTCTCTGTC[A/T]CACACACACACACAC | 68519 |
| rs579305182 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108390878 | TACATACATATCACA[C/T]ACAGATACACACTCA | 68519 |
| rs579311231 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486096 | ATAAGCAAGTATGAG[A/G]GCCAAGCAGCCCCGC | 68519 |
| rs579337782 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108524349 | TATCAGATTACCATG[A/G]CCTAAGGCTGATCTT | 68519 |
| rs579346093 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108531575 | TGAGTTTGAGGCCAG[C/T]CGGGTCTACAAAGTG | 68519 |
| rs579350163 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478471 | ACCCCAGAAGAGGGC[A/G]TCAGATCCCATTACA | 68519 |
| rs579357456 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522230 | CCAGGATCTCAGGAT[A/C]TCAGGATCCCAGGAT | 68519 |
| rs579358189 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465137 | TGCCTGCCTCTGCCT[A/C]CCAAGTGCTGGGATT | 68519 |
| rs579366138 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442490 | AAGTGAAAAAAATGT[A/G]CTTGCAGCTCTTTAC | 68519 |
| rs579368128 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471505 | GAAAGAGCAGGGAGG[A/G]GGAGCAAGGGAGGAG | 68519 |
| rs579400279 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471395 | GGGGAGCAGGAGAGG[A/G]GGAGCAGGGGAGGAG | 68519 |
| rs579406783 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485570 | ACACACACACATACA[C/T]ACACACACATATACA | 68519 |
| rs579450004 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485580 | ATACACACACACACA[C/T]ATACACACACACATA | 68519 |
| rs579455564 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523625 | AAAACACACCTCAGT[A/G]ACAAAGGCAGACACT | 68519 |
| rs579457143 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520264 | ACACAGACACACACA[C/G]ACACACACACACACA | 68519 |
| rs579459684 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108497433 | CTTCTGCGGCTGCTC[C/G]AGCCCAGCGTTTACA | 68519 |
| rs579461627 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474669 | GTGATAGGTGCAGCT[A/G]ATACCAAATCGATTC | 68519 |
| rs579470983 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461632 | GCTTGCTCAGCCTGC[A/T]CTCTTATAGAACCAA | 68519 |
| rs579488734 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108438999 | CTTAGACCTTTTCAA[A/T]ATATATATATATATA | 68519 |
| rs579506154 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108528402 | CTCATGTTCAGACTC[A/C]GCCTCCTCTCACCAG | 68519 |
| rs579551765 | snp | G/T | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108369651 | AGACTTTCCAGGGGG[G/T]CCCAGAACTAGTTTT | 68519 |
| rs579554313 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404972 | CATGTGCACGCGTAC[A/G]ACACACAAACTTCTA | 68519 |
| rs579602608 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443680 | TTTTTTTTTGAAAAT[G/T]CAACCCTACCGGGAT | 68519 |
| rs579634331 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523224 | AGCTAGAAGATCCTA[A/G]GCAGATGTCATACAG | 68519 |
| rs579641861 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108432020 | AGTAGTAAAATGTCA[A/G]CATCTTTTTTTTTTT | 68519 |
| rs579642223 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467261 | TGTCACATGTATGTC[A/C]TAAATGCTGAGTCCT | 68519 |
| rs579659019 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478569 | TCTTACCCACTGAGC[A/C]ATCTTACCAGCCCGG | 68519 |
| rs579683027 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489402 | AGAAGAAGAAGAAGA[A/C]GAAGAAGAAGAAGAA | 68519 |
| rs579690128 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108524970 | TGTGCTTGAAATTAG[A/C]ATTTTCTTAATGTTT | 68519 |
| rs579693355 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473060 | CACACACATACACCA[A/G]GCATACACACACATA | 68519 |
| rs579699461 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108459733 | AGATAGATAGACAGA[C/T]AGACAGACAGACAGA | 68519 |
| rs579701446 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506153 | AAACTAATTGAAAGG[A/G]ACATGGGGGTGGGGG | 68519 |
| rs579773780 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527348 | CACTCCTGAACTGGC[A/G]GTGGTCAGTACTCCC | 68519 |
| rs579822740 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523703 | AAGAAACAAGCTGGA[A/G]TAGCCATTCTAATAT | 68519 |
| rs579824780 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108498953 | TGACACCCTCTTCTG[G/T]TGTGTCTGAAGACAG | 68519 |
| rs579840200 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474967 | CAAACCAAACCAAAC[A/C]AAACCAAACCAAACC | 68519 |
| rs579843234 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461661 | AAGACTACCAGCCCA[A/G]AGATGGCACCACCCA | 68519 |
| rs579845222 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485432 | ACATGCACACACACA[C/T]ACACACACACACACA | 68519 |
| rs579881897 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518920 | TAGACACTGCTTTTC[C/T]AAGTCTTTGCTTCCA | 68519 |
| rs579890504 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471326 | AGGAGCAGGGGAGGA[A/G]GAGCAGGGGAGGAGG | 68519 |
| rs579950031 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384891 | GGTAGGGAGACTGAG[A/C]AATACCAGCCGTGGC | 68519 |
| rs579959733 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467939 | CTTTCTAGAGGAATA[A/G]AACTGATAGAATATA | 68519 |
| rs579999668 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453183 | TATATCTGTGTGTAC[A/G]TGTGTGTTTATGTGC | 68519 |
| rs580052712 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108430463 | ACATGGCAGTTCCTG[A/C]CTGTCTGTAACTCCA | 68519 |
| rs580060098 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525050 | TGAAATAATTTCTCT[C/T]CTAGAAACACTGATA | 68519 |
| rs580085110 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108393354 | GGAAGTTGAGATGCT[C/T]AGCACAAGGGTATTG | 68519 |
| rs580088742 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532074 | CCTTCCATTCCTAAG[A/G]GCCCAGGCCTGGGTC | 68519 |
| rs580102359 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522795 | GAGAGAATCTCAGGT[A/G]CAGAAGATACCATAG | 68519 |
| rs580106403 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443716 | TTTATCTCTTGCACA[C/G]CCAGGACAGACCACT | 68519 |
| rs580108221 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488631 | GCCCACAATGTCTGA[A/G]ATGGTGATGATGATG | 68519 |
| rs580110607 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472727 | CTAGGTTCACCTGAG[A/G]GACCCTGCCTCAATG | 68519 |
| rs580114775 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108457454 | CGGTATGTGTGAGTG[A/T]GTGAGTGTGTGTGTG | 68519 |
| rs580127181 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108417308 | CTTGCTGGTCTGATC[C/T]AGAGTGCTCAAGGTA | 68519 |
| rs580218838 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461567 | GGTCATAAAGCAGGA[A/G]CTGATGCAGAGGCCA | 68519 |
| rs580224136 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108438916 | GAGCTGTCAGACTGA[C/G]AGGAAAGGAGGGAAG | 68519 |
| rs580256531 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404755 | ACACACACGCGCACA[C/T]GAACACACACATGCA | 68519 |
| rs580300344 | snp | G/T | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108369380 | GGAGGAGGAGGAGGA[G/T]GAGGAGGAGGAGGAG | 68519 |
| rs580328964 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532748 | AAATAAATAAAAAAT[G/T]TAACTTTATTTTGAG | 68519 |
| rs580335200 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488661 | GGTGATGGTGATGGT[A/G]GGGATGATGGTGGTG | 68519 |
| rs580347747 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108528034 | ATCTGCTTCCAGCTC[C/T]AGAGGCTCTAGAAAC | 68519 |
| rs580360025 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520233 | TCTTCCCCACAACAC[A/C]CACAGACACACAGAC | 68519 |
| rs580362238 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485566 | ATTCACACACACACA[C/T]ACACACACACACATA | 68519 |
| rs580370308 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471362 | GGGAGGGGGAGCAGG[A/G]GAGGAGGAGCAGGGG | 68519 |
| rs580372645 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108425744 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTATTCGC | 68519 |
| rs580374678 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454389 | TTACCTGAACAACAG[C/T]AGCCATGTTTATAAG | 68519 |
| rs580392049 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108398464 | AGAAAGTGATCTCTA[C/T]CAGTTCAAACAGGGA | 68519 |
| rs580426425 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458514 | GTCCCTTTTCCTGTT[A/G]GGTCTCAGAGCATAA | 68519 |
| rs580443875 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108431617 | GCACACATTTAACAC[A/G]CTTATGCACAGACAC | 68519 |
| rs580464282 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525262 | GCCCTGGCTGTCCTG[A/G]AACTCACTTTGTAGA | 68519 |
| rs580467187 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472943 | AACACACATACCACA[A/C]CACACACACATACAC | 68519 |
| rs580476767 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108391028 | CATAGACTGATAGGC[A/G]CATACACACACCACA | 68519 |
| rs580538582 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108377359 | TCTTTCTCCTTCTGG[A/G]TTCGGGTAAGTTATG | 68519 |
| rs580570747 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108425850 | GTGTGTGTGTCTGTG[G/T]TGTGTGGGGCAGTGC | 68519 |
| rs580582941 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454613 | CTTCCTTTCTTTCTT[C/T]CTTCCTTCTTTCTAT | 68519 |
| rs580618923 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108388345 | CCTCATGCCCTCACC[G/T]CCACCACACACACAC | 68519 |
| rs580675864 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442174 | GACCAAACGTGGGGA[A/T]ATGGTAAAAATGGGC | 68519 |
| rs580720180 | snp | G/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108536719 | ACCCACAGGAACACA[G/T]GACACTTGACTTACT | 68519 |
| rs580721781 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523929 | GAGACTCCAACACCC[A/C]ACTCTCATCAATGGA | 68519 |
| rs580733205 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108502520 | GCCAGGCCACTGGTA[C/T]TCAGACAACAAACAG | 68519 |
| rs580738445 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381020 | ACAGGGAGAGGGGCG[A/G]GGAGCAGTAACAGGG | 68519 |
| rs580738855 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108477363 | AGAGGGAGAGGGAGA[A/G]AGAGAGTTGCCTCAT | 68519 |
| rs580738920 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407389 | CAGAGATATAGAGAG[A/G]CATAGAGAAAGAGAT | 68519 |
| rs580742840 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108463430 | ACCATCGTCTTAGGT[C/T]GGCAGAGTGTATCAC | 68519 |
| rs580754272 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108516866 | AGAACCTCTAGAATC[C/G]AACATGCTTCGTGCA | 68519 |
| rs580767868 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480348 | CTTTCTTTCCTTCCT[C/T]CCTCCTTCCCTCCCT | 68519 |
| rs580778026 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446881 | CCCCCTGTGCAGAAG[A/G]GCTAGCATGTGTGTG | 68519 |
| rs580808869 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418496 | GGCCCTTCCCCCTTG[A/T]TCACTAATTGAGAAA | 68519 |
| rs580826512 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108483799 | GTGGTTTAAGCACAC[G/T]GGCTGCTCTTGCAGA | 68519 |
| rs580836925 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108470341 | TTTGACAAACTTGTA[A/G]AGTTCTTAATGAGAC | 68519 |
| rs580840514 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523393 | ATAATAGATGGGAAA[C/T]ACCAACACAAGGAGG | 68519 |
| rs580840746 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108492692 | CTCAGTGTTCCAAGT[C/G]CTGAGACTGCAGAAA | 68519 |
| rs580846720 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525496 | AGTTATGGATAGTAG[A/T]AAATATTCATTAATG | 68519 |
| rs580941635 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478362 | TTAAGAATGTTTAAA[A/G]ATTTCTTTATTCTTT | 68519 |
| rs580943596 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520320 | ACACACAGACACACA[C/G]ACACACAGACACACA | 68519 |
| rs580946520 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108503814 | ATGCCATTGTATGGG[A/C]GTTAGTCTTAGCACC | 68519 |
| rs580956819 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465122 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 68519 |
| rs581003471 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485656 | ATACACACACACATA[C/T]ACACACACACATACA | 68519 |
| rs581009065 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471442 | GCAGGGGAGAAAGAG[C/G]AGGGAGTGGGAGCAG | 68519 |
| rs581012848 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455070 | TGTGTGCATGTGTGT[A/G]CATGTGTGTGTGTGC | 68519 |
| rs581024859 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108426539 | TGTTTTTTGTTTTTT[G/T]TTTTTTGAGACAGGG | 68519 |
| rs581103024 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108524087 | CTCAGCACCTCATTC[G/T]AGCTTCTCCAAAATT | 68519 |
| rs581133985 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517898 | AGAAGCAGAGGCAGA[A/G]GCAGAGGCAGAGGCA | 68519 |
| rs581146264 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433494 | GGAAGTGATTGGATG[A/G]AGTTGGGCTCTCTCT | 68519 |
| rs581164496 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108459745 | AGACAGACAGACAGA[C/T]AGACAGATAGATATA | 68519 |
| rs581200089 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108526144 | TTTGAACTTCACAGG[A/G]GAAACAGATTTCTTA | 68519 |
| rs581213505 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108420484 | TTCCTTCCTTCCTTC[C/T]CTCCCTCCCTCCTTC | 68519 |
| rs581216743 | snp | A/C | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402059 | TGTGTGTGTGACTTA[A/C]TGTGTAGCTCTGGCC | 68519 |
| rs581259499 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523904 | ATCACACCCCACATG[A/G]TAATAGTGGGAGACT | 68519 |
| rs581263096 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108535885 | GTTGAAGAGGCTGAG[A/G]GGTGTGTGTGTGTGT | 68519 |
| rs581272073 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523268 | ACAAATGCCAACCCA[A/G]GCTACTATACCCAGC | 68519 |
| rs581282339 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489498 | GGAGGAAGAGGAAGA[A/G]GAAGAGGAAGAGGAG | 68519 |
| rs581284302 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473117 | ACATACCACACCACA[C/T]CATACACACACCACA | 68519 |
| rs581312361 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108390486 | AATAATAAAAAAATT[A/T]AAAAATACACATTTT | 68519 |
| rs581340093 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474996 | CCAAATCAAATCAAA[A/T]CAAAACAAAAACAAA | 68519 |
| rs581354245 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441315 | CCTCGGTAGAAAAGC[A/G]GGTTCTCGGACCACT | 68519 |
| rs581383193 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522007 | ACCAGTGGGACCCAG[A/G]CACCCAGGAACTCCG | 68519 |
| rs581389149 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471488 | GGAGGAAGAGCAGGG[A/G]AGAAAGAGCAGGGAG | 68519 |
| rs581400014 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108429128 | TTTACGTGGTGTGTG[C/T]GTGTGTGTGTGCGCG | 68519 |
| rs581414240 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108501379 | CCCTTCTGTTGATGG[A/G]CATATGGCTGGTTCT | 68519 |
| rs581428117 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461700 | CCTCCCCCCTTGATC[A/T]CTAATTGAGAAAATG | 68519 |
| rs581454101 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460395 | ATAGGAGATGGATGT[C/T]CCGCCCTTATGTGGA | 68519 |
| rs581475424 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455086 | CATGTGTGTGTGTGC[A/G]TGTGTGTGTATGTGT | 68519 |
| rs581497551 | snp | C/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108406500 | CCGCACCCCTCCCCC[C/G]CAGTCTCCTTTCTAA | 68519 |
| rs581502801 | snp | A/G | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | GRCm38.p3 | 12:108536140 | ATGGGAAGGTGGGTG[A/G]TCTTCCCTGTGGCTC | 68519 |
| rs581505947 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108479600 | AATTATTCCTTTGCT[A/T]TTTGGTAGGCATATT | 68519 |
| rs581537936 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473142 | ACCACACCACACACA[A/C]CAAGCGTAGACACAC | 68519 |
| rs581564874 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506167 | GGACATGGGGGTGGG[A/G]GTGGGGTGGAGGGAC | 68519 |
| rs581573680 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433950 | CCAGCAGAGAGTGTG[C/T]GCTCGTGTGTGTGTG | 68519 |
| rs581595495 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523375 | AATCCAGCCCTACAA[A/T]GGATAATAGATGGGA | 68519 |
| rs581666417 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468501 | AGGAAGAGGAAGAAG[A/G]AGAGGAGGAGGAAGA | 68519 |
| rs581671776 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108445419 | CCTTGGGGGCTGGAC[A/G]TGTTGGGCGTTACCC | 68519 |
| rs581677953 | snp | G/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403204 | ACCGTCTTTATCTTT[G/T]TTGTTGTTTTTTTTG | 68519 |
| rs581680552 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522607 | CCCTTAAAGAATTAC[A/G]GGAAAACACAACCAA | 68519 |
| rs581692208 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471506 | AAAGAGCAGGGAGGG[A/G]GAGCAAGGGAGGAGG | 68519 |
| rs581735417 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418389 | GCTGATGCAGAGGCT[A/G]TGAAGGGATGTTCTT | 68519 |
| rs581750390 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108391002 | CCATAGTACACCATA[G/T]ACAAACACTACATAG | 68519 |
| rs581750733 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108530591 | GTCCTCTCTGTTTTT[C/T]CAGACAGGGTTTCTC | 68519 |
| rs581792441 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485386 | ACACACACACACACA[C/G]AGGCACCCACTCATT | 68519 |
| rs581802737 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452938 | TGTGTGTGTGTGTGT[A/G]TGTGTGTATGTGTAT | 68519 |
| rs581805842 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455564 | GCCACCTCCTTTGTG[A/G]ACAGCGTCAACCATG | 68519 |
| rs581816432 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108384569 | TTGCTCATCCAGGTT[A/T]TCACAACCCTATCAG | 68519 |
| rs581832318 | snp | A/C | | | intron-variant, utr-variant-5-prime | Eml1, Gm33385 | GRCm38.p3 | 12:108411209 | CCAAAGCCTTCATCG[A/C]TGTCTGTATTCCTCA | 68519 |
| rs581846119 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486110 | GGGCCAAGCAGCCCC[A/G]CTCTGCTTGTAGCAG | 68519 |
| rs581849771 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527341 | CAATGTCCACTCCTG[A/C]ACTGGCGGTGGTCAG | 68519 |
| rs581851024 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465571 | CTAAAATCTCCTTAT[G/T]TTTGAAGAGTCTGGG | 68519 |
| rs581856875 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443376 | ACTGACTCTCACTGA[A/G]TCCGTCGCTTCTCCT | 68519 |
| rs581897720 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518038 | AAATAAATAAATAAA[C/T]AAATAAAACAAAAGA | 68519 |
| rs581909989 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471303 | CTGAGGAGCAGGAGC[A/C/T]GGGGAGGAGGAGCAG | 68519 |
| rs581939295 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108421710 | CTCTGGCTGTCCAGG[C/T]CACACCCAACCTCAG | 68519 |
| rs582018704 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473340 | AGCACACACACATAC[A/T]TACCACACCACCCAT | 68519 |
| rs582028470 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461038 | ATAGACAGACAGGTA[G/T]ATAGATGATAAATAG | 68519 |
| rs582047082 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532052 | ACTAACCTTCTTCTG[A/C/T]CTTAAACCTTCCATT | 68519 |
| rs582047103 | snp | A/C | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407447 | GAGACACAGAGAGAT[A/C]GAGAGACGGATAGAG | 68519 |
| rs582093225 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403283 | GGTTTCTCTGTGTAG[C/T]CCTGGCTGTCCTGGA | 68519 |
| rs582101234 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108434756 | ACATATACCATGTAC[C/T]ACACACACATACATA | 68519 |
| rs582152085 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519641 | CCTTACTACTGCATC[C/T]GGATTTTTTTGTTTT | 68519 |
| rs582168118 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376335 | TTCGTCACCCTTCTC[C/T]TCCCCGCCTTTTTTT | 68519 |
| rs582209498 | snp | A/G | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108369337 | ATGGGGAGAAGGAGG[A/G]GGAAGAAGAGGGGGA | 68519 |
| rs582244158 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474210 | TCACCATCAGCCAGG[C/T]ATGGTGGTGCACGCC | 68519 |
| rs582263852 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522790 | TAGAAGAGAGAATCT[C/T]AGGTACAGAAGATAC | 68519 |
| rs582269725 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108487891 | TCTACCCAGTAGCAA[A/C]CCCCCCCCCCCATTT | 68519 |
| rs582272069 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108391091 | ACAGACAGACAGACA[C/G]ACAGACACACACCCC | 68519 |
| rs582279696 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108430461 | CCACATGGCAGTTCC[C/T]GACTGTCTGTAACTC | 68519 |
| rs582283519 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456778 | GGCTGGCCTCGAACT[C/T]AGAAATTCGCCTGCC | 68519 |
| rs582286617 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527408 | TCCTACAGGGCCAGA[C/G]GACAGAGAGAGATCC | 68519 |
| rs582354498 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108524339 | CCATGCATCCTATCA[C/G]ATTACCATGGCCTAA | 68519 |
| rs582356398 | snp | A/C | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403711 | ATAACTTTAAAAAAA[A/C]AACCACACATTTAGA | 68519 |
| rs582358655 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458429 | GACTGTGTGTGCATC[G/T]CACAGGAGGATCATG | 68519 |
| rs582365148 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478374 | AAAGATTTCTTTATT[A/C]TTTATTCTTTATTAT | 68519 |
| rs582381820 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485481 | CACAGAGGCACCCAC[A/T]CATTCACACACATAC | 68519 |
| rs582381980 | snp | C/T | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108536929 | TGTGTACTCAGGCCT[C/T]TAATATACAATGCTC | 68519 |
| rs582387720 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471340 | AAGAGCAGGGGAGGA[A/G]GAGCAGGGGAGGGGG | 68519 |
| rs582389784 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494870 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGC | 68519 |
| rs582391184 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461099 | TAGGTAGATAGATAG[A/G]TAGATAGATAGATAG | 68519 |
| rs582391410 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108397233 | CATTCTATTGGGTTG[A/G]GGGTGGAGGGGGCAT | 68519 |
| rs582500987 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472825 | CACAAATGCAATATA[C/T]ACACACCACACCTCA | 68519 |
| rs582502791 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108503822 | GTATGGGCGTTAGTC[C/T]TAGCACCCTGGCTGG | 68519 |
| rs582515966 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465126 | ACTCAGAAATCTGCC[C/T]GCCTCTGCCTCCCAA | 68519 |
| rs582545428 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108431395 | AGGGACAGCAGTCTG[C/T]ATCTATAGCCCACCC | 68519 |
| rs582569638 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488635 | ACAATGTCTGAGATG[A/G]TGATGATGATGGTGA | 68519 |
| rs582589407 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442473 | ACCACTCCTCAGCAG[A/G]AAAGTGAAAAAAATG | 68519 |
| rs582610852 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108496200 | CAAGGGGTTAGAAAC[A/G]GCTTGCCTGGGGCTG | 68519 |
| rs582621120 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532172 | ATGCTTTGTGGGTGG[C/T]ATTTGTGTGAACACT | 68519 |
| rs582622359 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108420497 | TCCCTCCCTCCCTCC[C/T]TCCTTCCTATCTTTT | 68519 |
| rs582626199 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461617 | GGCTTGCCTCCCCTG[A/G]CTTGCTCAGCCTGCT | 68519 |
| rs582629267 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522863 | CAAAAAGCTCCTGAC[A/C]CAAAACATCCAGGAA | 68519 |
| rs582661587 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376409 | GTCTTCAGACACATC[A/G]GAAGAGGGCATCAGA | 68519 |
| rs582752927 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523616 | TGCATACAGAAAACA[C/T]ACCTCAGTGACAAAG | 68519 |
| rs582764778 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108382301 | TAATCCCCAGCACCT[C/T]TGCAAAAAGCCAGGC | 68519 |
| rs582765035 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474427 | TTCGGAAAGATCTCA[A/T]CCTTTTGGGACTCTT | 68519 |
| rs582782320 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471147 | TTGATCCGCACGCAA[A/C/T]GCTGTGAGAGCTGAC | 68519 |
| rs582784676 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108438920 | TGTCAGACTGAGAGG[A/G]AAGGAGGGAAGGAGA | 68519 |
| rs582838339 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108526248 | AATGCATCGTACAAT[A/C]CACACACACACACAC | 68519 |
| rs582842298 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517937 | GGCAGAGGCAGAGGC[A/T]GGAGGATCTCTGTGA | 68519 |
| rs582847116 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485266 | CCCTGATGTCTTAGG[G/T]ACCTCAGCTCCTGTG | 68519 |
| rs582847287 | snp | A/G | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108369382 | AGGAGGAGGAGGAGG[A/G]GGAGGAGGAGGAGGA | 68519 |
| rs582851310 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404941 | GCACGTGCACACGTA[C/T]GCATGCACATACACA | 68519 |
| rs582889865 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108531587 | CAGTCGGGTCTACAA[A/T]GTGAGTTCCAGGACA | 68519 |
| rs582899554 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108534034 | TCCACTGAGGTGGAC[C/G]CCCCAGGAGGATATG | 68519 |
| rs582948977 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108524643 | AAAAGACGCAAATAC[C/T]CCCAAGAGGAGTAGA | 68519 |
| rs582953005 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108504789 | CGACATATTTTTTTA[C/T]TTTGGCCCTTTTATT | 68519 |
| rs582961283 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478505 | GGTTGTGAGCCACCA[C/T]GTGGTTGCTGGGATT | 68519 |
| rs582966833 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485625 | CACAGAGGCACCCAC[A/T]CATTCACACACACAC | 68519 |
| rs582980734 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454615 | TCCTTTCTTTCTTCC[C/T]TCCTTCTTTCTATTC | 68519 |
| rs583038828 | snp | A/T | | | intron-variant, downstream-variant-500B | Eml1, Gm33385 | GRCm38.p3 | 12:108400264 | CCTCGTGACCCACAG[A/T]GCCTCAATAGGAATA | 68519 |
| rs583132199 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520288 | ACACACACACACACA[C/G]ACACACACACACACA | 68519 |
| rs583144701 | snp | A/G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471424 | AGGAGCAGGGGAGGA[A/G/T]GAGCAGGGGAGAAAG | 68519 |
| rs583165968 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461633 | CTTGCTCAGCCTGCT[C/G]TCTTATAGAACCAAG | 68519 |
| rs583177701 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467599 | TCCGAATGTTTATGC[C/T]TTTGTGTGATTCTGT | 68519 |
| rs583197007 | snp | A/G | | | intron-variant, upstream-variant-2KB | Eml1, Gm33385 | GRCm38.p3 | 12:108412795 | CAGAGAAACTATCGA[A/G]AGAGAGAGAGAGAGA | 68519 |
| rs583216146 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108405063 | ATATGACTCTGCAAG[C/T]CTAGTCTGCCCAAGG | 68519 |
| rs583216304 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523680 | TTATTTTCCAAGCAA[A/G]TGGTCCCAAGAAACA | 68519 |
| rs583222490 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108439381 | GGGCTGGTTGAACTT[A/G]CAACCTTACTACTGC | 68519 |
| rs583227178 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108497656 | GTGATATTAGCAATG[C/T]ATCTGCTTTTTTTTT | 68519 |
| rs583229142 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108388484 | TCCCTGGGGGGCTAT[A/G]GCCAGGGACCCGGGA | 68519 |
| rs583233335 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474937 | CCTGTCTTGAAAAAC[A/C]AAACCAAACCAAACC | 68519 |
| rs583264038 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525009 | AGAGTTTTGCTATTT[C/T]GAAAATTTTAAAATA | 68519 |
| rs583280258 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474981 | CCAAACCAAACCAAA[C/T]CAAATCAAATCAAAT | 68519 |
| rs583319358 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108535072 | TCCTTGTGACATGAG[A/G]ATTTGGCCTTACAGC | 68519 |
| rs583333099 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523261 | AGAGAACACAAATGC[C/T]AACCCAAGCTACTAT | 68519 |
| rs583344100 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478570 | CTTACCCACTGAGCC[A/T]TCTTACCAGCCCGGC | 68519 |
| rs583363648 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443687 | TTGAAAATGCAACCC[C/T]ACCGGGATGGCTGTT | 68519 |
| rs583371946 | snp | A/G | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108370859 | AACTGAAGTTGGGTG[A/G]CTGTGCTCGGTGTGC | 68519 |
| rs583376037 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108378606 | GTACATGAAGGCAGA[C/G]GGTGGGTGTCTGAGT | 68519 |
| rs583426736 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473076 | GCATACACACACATA[C/T]CACACTACACACCAA | 68519 |
| rs583430786 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108459737 | AGATAGACAGACAGA[C/T]AGACAGACAGACAGA | 68519 |
| rs583467769 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461691 | ACAAGGGGACCTCCC[C/T]CCTTGATCTCTAATT | 68519 |
| rs583493134 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108405819 | AATGTCCTCTGAATT[A/G]CTCTGAAGTTGGTCT | 68519 |
| rs583519036 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525103 | ATCGTTTTAAAGTAA[A/G]CTTATAGTTAGACAA | 68519 |
| rs583538974 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523795 | GGTTAAAAGAAAAAT[C/T]TACCAAGATAAACTC | 68519 |
| rs583607843 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108385924 | GGCAGCTTCAGTCGG[A/G]CTTCCTGTTTCTGTG | 68519 |
| rs583613712 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108423930 | AGTCTCTGTAGCAGG[A/G]TTGGGAAAGATTTTT | 68519 |
| rs583620178 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108453445 | CTGGCTGGCCACTAA[A/G]CCTTGGTTGGAATCC | 68519 |
| rs583640090 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108501380 | CCTTCTGTTGATGGA[C/T]ATATGGCTGGTTCTA | 68519 |
| rs583706105 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108425753 | GTGTGTATGTGTGTG[C/T]ATTCGCATATATGGA | 68519 |
| rs583714565 | snp | C/G | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | GRCm38.p3 | 12:108536089 | AGACCCAGATTTGCA[C/G]CCATCTCCAGACAAA | 68519 |
| rs583724642 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108508614 | GACATGTCTGTGACT[C/G]CAGAGCAAGGGAGGT | 68519 |
| rs583741584 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108444113 | TTTTCTTGATAGGGT[C/T]TTCCTATGTAGCCCT | 68519 |
| rs583794376 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379202 | GTTTGTGTATGTGGG[C/T]ACAGATCATGTGTGT | 68519 |
| rs583795822 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108479061 | TGTTTTGCAGGTATG[A/T]ACGTGTGTGTGTGTG | 68519 |
| rs583801593 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418055 | TTGAGATTCTCTGAT[A/G]ACTGTGTGTCTGTTT | 68519 |
| rs583805957 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467942 | TCTAGAGGAATAAAA[C/T]TGATAGAATATATAT | 68519 |
| rs583806897 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523305 | CTCAATTACCATAGA[C/T]GAAGAAACCAAGATA | 68519 |
| rs583828247 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523920 | TAATAGTGGGAGACT[A/C]CAACACCCAACTCTC | 68519 |
| rs583831512 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523195 | ACACCAGACTTCTCA[A/C]CAGAGACTATGAAAG | 68519 |
| rs583843607 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446542 | ATCAGCCAAGGTCAT[A/C]CAGGGAGACTCTAAG | 68519 |
| rs583847722 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472986 | CACACACACACACCC[A/C]ACACCATACACACAC | 68519 |
| rs583863848 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108431622 | CATTTAACACGCTTA[C/T]GCACAGACACGGACA | 68519 |
| rs583888941 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108387635 | ATCCTCCCGGCAAGC[A/G]AACAAATCCTTCTCC | 68519 |
| rs583905936 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108528056 | TCTAGAAACGCTCCC[A/G]GAATTCTGCTCTAGA | 68519 |
| rs583917075 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461765 | ACTGAAGCTCCTTTC[A/T]CTGTGATAACTCCAG | 68519 |
| rs583918846 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520238 | CCCACAACACCCACA[C/G]ACACACAGACACACA | 68519 |
| rs583932781 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454442 | CTCTCTCTCATCCTT[C/T]CCCTCCCTCCCTCCC | 68519 |
| rs583990807 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108531608 | TTCCAGGACAGCCAG[A/G]GCTATACAGAGAAAC | 68519 |
| rs583993926 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485568 | TCACACACACACATA[C/T]ACACACACACATATA | 68519 |
| rs584001056 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486407 | CACCAGTGCTCTGCA[C/T]CAGTGGCAGCCTGGT | 68519 |
| rs584001984 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471390 | GGGAGGGGGAGCAGG[A/G]GAGGAGGAGCAGGGG | 68519 |
| rs584044150 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489381 | ATGGGGAGGAGGTGG[A/T]GAAGAAGAAGAAGAA | 68519 |
| rs584046390 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522880 | AAAACATCCAGGAAA[C/T]CCAGGACACAATGAG | 68519 |
| rs584051418 | snp | G/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407392 | AGATATAGAGAGGCA[G/T]AGAGAAAGAGATAGA | 68519 |
| rs584052076 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458667 | CTCAGTAAGTAGTGT[A/G]TGTGTGTATGTGTAC | 68519 |
| rs584076053 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456413 | CTACTCTCAGCCTTG[C/T]AGGCCAGTTCACATC | 68519 |
| rs584117805 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480206 | CTGTGTGCACACACA[C/T]GTGAGGTGCAAGTGT | 68519 |
| rs584159392 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108528050 | AGAGGCTCTAGAAAC[A/G]CTCCCAGAATTCTGC | 68519 |
| rs584186144 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517542 | CTGTCTCCACCTACA[C/T]CTGTGCGGGGGGCCA | 68519 |
| rs584187964 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525296 | GGCTGGCCTCGAACT[C/G]AGAAATCCTCTTGCC | 68519 |
| rs584188335 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108515464 | AGGTTAGGATACAAT[A/G]ATAAAGTTAATCACT | 68519 |
| rs584194509 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522707 | AAGGGAGACAACCCT[A/G]GAGTTAAAAAACCTA | 68519 |
| rs584202562 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471507 | AAGAGCAGGGAGGGG[A/G]AGCAAGGGAGGAGGA | 68519 |
| rs584202742 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108470342 | TTGACAAACTTGTAA[A/G]GTTCTTAATGAGACC | 68519 |
| rs584215925 | snp | A/G | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108369284 | ACAGTAAGAGGAGGA[A/G]GGGGAGGAGGGGGGG | 68519 |
| rs584251687 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376239 | TCTTTTCCTCCTCCT[C/T]CTCCTCCTCCTCCTC | 68519 |
| rs584281242 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108419638 | CTCTCCCTCCTCCTC[C/T]CCCAACAGCATTGTG | 68519 |
| rs584293844 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523933 | CTCCAACACCCAACT[C/T]TCATCAATGGACATA | 68519 |
| rs584298988 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108503804 | GCTTTCGGAAATGCC[A/G]TTGTATGGGCGTTAG | 68519 |
| rs584364711 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108429968 | TTCTGAAGGCGTTCC[C/T]TCCAGTGACTCAGTC | 68519 |
| rs584376194 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478284 | ACTTCACTCACGTCC[C/T]ACATAGTGTGTGGGG | 68519 |
| rs584382259 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108464778 | TGGGTTTACAGGTTA[G/T]GGTTCTAGTGCTAGA | 68519 |
| rs584388542 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442175 | ACCAAACGTGGGGAA[A/C]TGGTAAAAATGGGCA | 68519 |
| rs584400251 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525745 | TTCTGAATTCGAGGC[C/T]AGCCTGTCTAACAAA | 68519 |
| rs584414405 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108482412 | GCACCACACAGCACT[C/T]GCGCACTCGTGCACA | 68519 |
| rs584420469 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471143 | GGGTTTGATCCGCAC[G/T]CAATGCTGTGAGAGC | 68519 |
| rs584423085 | snp | A/C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108448153 | TGTGTGTGTGTGTGT[A/C/G]TGTGTGTCTGTCTGT | 68519 |
| rs584435770 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108524182 | CGGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 68519 |
| rs584437722 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403378 | TGGGATTAAAGGCGT[A/G]CGCCACCACTGCCTG | 68519 |
| rs584452157 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478363 | TAAGAATGTTTAAAG[A/T]TTTCTTTATTCTTTA | 68519 |
| rs584462999 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442214 | AGGTTTCTGAATGCA[A/T]AACCACCAAAAATGT | 68519 |
| rs584489068 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108494661 | CATAGCTTTGATCTA[C/T]GGAACACAGACACTC | 68519 |
| rs584492468 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381034 | GGGGAGCAGTAACAG[G/T]GAGAGAGGCAGGTAG | 68519 |
| rs584499308 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461051 | TAGATAGATGATAAA[C/T]AGATTGATAGATAGA | 68519 |
| rs584544701 | snp | A/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108536728 | AACACATGACACTTG[A/G]CTTACTTACCTACCG | 68519 |
| rs584551349 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108526165 | AGATTTCTTATCAGA[A/G]AGTCAAAAATCCCTT | 68519 |
| rs584552387 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523490 | TAACAACAAAAATAA[C/G]AGGAAGTAACAATCA | 68519 |
| rs584640824 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489507 | GGAAGAAGAAGAGGA[A/G]GAGGAGGAAGAGGAG | 68519 |
| rs584654604 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108459749 | AGACAGACAGACAGA[C/T]AGATAGATATAGGAT | 68519 |
| rs584674460 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108530568 | ACAAATCCCCCGCCC[A/G]CTGTCTAGTCCTCTC | 68519 |
| rs584684657 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108408304 | GTACAATCACAATCA[C/T]GCACACACTCACACA | 68519 |
| rs584753502 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471496 | AGCAGGGGAGAAAGA[A/G]CAGGGAGGGGGAGCA | 68519 |
| rs584781782 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108427199 | TTTCTATGTTATGTG[G/T]TAACACTGGGTTTAT | 68519 |
| rs584783921 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520597 | TTTAAGAAAATTTTG[G/T]TGGTGGTTGGGTTTT | 68519 |
| rs584788222 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485684 | ACACACACACATACA[C/T]GCACACACACATACA | 68519 |
| rs584846216 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433743 | TCAGACGGTCAGTGC[C/T]GTGGGGAGGAACAGA | 68519 |
| rs584888605 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108531668 | CAAACAAACAAAAAA[A/C]AAAAACAAAGACAAA | 68519 |
| rs584889059 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473122 | CCACACCACATCATA[A/C]ACACACCACACCACA | 68519 |
| rs584889648 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484270 | AGGGCCTGGTTAGGC[A/G]ACCGGTAGAGAGGGC | 68519 |
| rs584897511 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517920 | GCAGAGGCAGAGGCA[A/G]AGGCAGAGGCAGAGG | 68519 |
| rs584910704 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484293 | GAGAGGGCGTGAACT[A/G]GAGCCACTAACCCAG | 68519 |
| rs584971018 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108420485 | TCCTTCCTTCCTTCC[C/T]TCCCTCCCTCCTTCC | 68519 |
| rs584974867 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108383783 | TAAAACTTTCTTCCA[A/T]AAAATTATTTGAATC | 68519 |
| rs584990119 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471145 | GTTTGATCCGCACGC[A/G]ATGCTGTGAGAGCTG | 68519 |
| rs584992683 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523382 | CCCTACAATGGATAA[G/T]AGATGGGAAACACCA | 68519 |
| rs584999174 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108451337 | TGCAGATATACACAC[A/G]CACACACACACACAC | 68519 |
| rs585003919 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473178 | TACCATACCATACCA[C/T]ACCACACACACACAT | 68519 |
| rs585014041 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455259 | TCTGGATCAGCACTA[G/T]GTGTCAGCGTGGTGA | 68519 |
| rs585030047 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108390505 | AATACACATTTTCAA[A/G]CAGTATTTTAAGAGT | 68519 |
| rs585119566 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108486095 | GATAAGCAAGTATGA[C/G]GGCCAAGCAGCCCCG | 68519 |
| rs585158409 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108372997 | AGAGAGAGAGAGACC[A/T]TTTCCCAAACAACAA | 68519 |
| rs585164601 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407346 | GAGGGGAGAAAAGAG[A/G]TGAGAGAGAGGAAGA | 68519 |
| rs585171370 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108530684 | ATTCCCCCTGCCTCC[A/G]CCTCTCAAGTGCTGG | 68519 |
| rs585212447 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108397237 | CTATTGGGTTGGGGG[G/T]GGAGGGGGCATTCCG | 68519 |
| rs585264431 | snp | A/G | | | intron-variant, nc-transcript-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108536702 | TATGTGGATGATGTT[A/G]TACCCACAGGAACAC | 68519 |
| rs585273598 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108499920 | AGAAGGGAGGGGGGA[A/G]AATCAAACATTCACA | 68519 |
| rs585274738 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108491906 | AGATTTTTTTTTTAA[C/T]TTTAAAAAAGTTTTA | 68519 |
| rs585282406 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108526313 | ACACACACACACCCT[A/G]GACCTTCCGGTTGAA | 68519 |
| rs585340102 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518644 | TCCAGACATAAGACT[G/T]TTATGTATGCCTGAA | 68519 |
| rs585351930 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471311 | CAGGAGCAGGGGAGG[A/G]GGAGCAGGGGAGGAA | 68519 |
| rs585352725 | snp | A/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108403215 | CTTTTTTGTTGTTTT[A/T]TTTGTTTTTTGTTTT | 68519 |
| rs585359631 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108434700 | CTACACACACACATA[C/T]ATACACACACATACC | 68519 |
| rs585364135 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460398 | GGAGATGGATGTCCC[A/G]CCCTTATGTGGATAC | 68519 |
| rs585375795 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108518030 | CCATCTCAAAATAAA[C/T]AAATAAATAAATAAA | 68519 |
| rs585375938 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485267 | CCTGATGTCTTAGGG[A/C]CCTCAGCTCCTGTGC | 68519 |
| rs585393184 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443404 | CCTCCAGTCCCCCCC[C/T]CCCTCCCTGCTTTGT | 68519 |
| rs585433674 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525031 | TTTAAAATATACTTA[C/T]TGATGAAATAATTTC | 68519 |
| rs585444876 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478574 | CCCACTGAGCCATCT[C/T]ACCAGCCCGGCTTTT | 68519 |
| rs585492596 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108505494 | AACACACAAAAAAGT[A/C]TTATTTAGCATTCTT | 68519 |
| rs585499809 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478511 | GAGCCACCATGTGGT[A/T]GCTGGGATTTGAACT | 68519 |
| rs585506229 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465860 | TGGGGGCGGAGCTGC[G/T]CATCTGAGGCTCTGG | 68519 |
| rs585526015 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108443690 | AAAATGCAACCCTAC[A/C]GGGATGGCTGTTTAT | 68519 |
| rs585590999 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452946 | TGTGTGTGTGTGTGT[A/G]TGTGTATGTGTGTGT | 68519 |
| rs585643298 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108495202 | GGTGTCTTTTGGCTT[C/T]CTGTCTGGCTCCAGC | 68519 |
| rs585647991 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527342 | AATGTCCACTCCTGA[A/C]CTGGCGGTGGTCAGT | 68519 |
| rs585654156 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485418 | ACACACACACATACA[A/C]ATGCACACACACATA | 68519 |
| rs585656775 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461472 | GACCAAGAAGCAAGT[A/T]GGGGAGGAAAGGGTT | 68519 |
| rs585704519 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1 | GRCm38.p3 | 12:108422755 | GCAGTTGTCCGGGGT[C/T]CCGGGGGGGGGGGAC | 68519 |
| rs585725193 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404653 | AAACACACACATGCA[C/T]GTGCAAATACACACA | 68519 |
| rs585752607 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523689 | AAGCAAATGGTCCCA[A/T]GAAACAAGCTGGAGT | 68519 |
| rs585756723 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108498463 | CTGTGCTCAGCAGTG[A/G]CATTCCCTTATGGGC | 68519 |
| rs585764881 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474951 | CCAAACCAAACCAAA[C/T]CAAACCAAACCAAAC | 68519 |
| rs585773070 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461644 | TGCTCTCTTATAGAA[A/C]CAAGACTACCAGCCC | 68519 |
| rs585773896 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108467793 | ATTCTATTAAAGCAC[A/G]TGGATAGAGATGTGT | 68519 |
| rs585811819 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532065 | TGACTTAAACCTTCC[A/G]TTCCTAAGGGCCCAG | 68519 |
| rs585824649 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108522792 | GAAGAGAGAATCTCA[G/T]GTACAGAAGATACCA | 68519 |
| rs585839797 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108416766 | GGGCCTACATTCACC[C/T]CTTGGCTATATCATC | 68519 |
| rs585877847 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108430462 | CACATGGCAGTTCCT[A/G]ACTGTCTGTAACTCC | 68519 |
| rs585882281 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379162 | TATAGTGTGCGTGTG[C/T]GTGTGTGTGTGTGTG | 68519 |
| rs585897408 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108472850 | ACCTCACATATACCA[C/T]ACCACACCACACACA | 68519 |
| rs585900395 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488598 | GGTCACATCCTGGAA[A/G]CTGTAACTTGACTTC | 68519 |
| rs585909301 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108431599 | ACACATACACAGACA[G/T]GTGCACACATTTAAC | 68519 |
| rs585914717 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108456785 | CTCGAACTTAGAAAT[C/T]CGCCTGCCTCTGCCT | 68519 |
| rs585972820 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523581 | CAGACTGGATACATA[A/G]ACAGGACCCAGCATT | 68519 |
| rs585981754 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474219 | GCCAGGCATGGTGGT[A/G]CACGCCTTTAATCCC | 68519 |
| rs585999193 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108438107 | AAAAGGCTGTACTGT[C/T]TTTATCTTGTGAATC | 68519 |
| rs586001559 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523624 | GAAAACACACCTCAG[C/T]GACAAAGGCAGACAC | 68519 |
| rs586018148 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485494 | ACTCATTCACACACA[C/T]ACATACACACACACA | 68519 |
| rs586019877 | snp | C/T | | | intron-variant | Eml1, Gm16596 | GRCm38.p3 | 12:108537761 | CTCTCTGCCTACCTA[C/T]TCCCCATCTCCCCAC | 68519 |
| rs586021921 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471353 | GAGGAGCAGGGGAGG[A/G]GGAGCAGGAGAGGAG | 68519 |
| rs586028416 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454386 | TGGTTACCTGAACAA[C/G]AGTAGCCATGTTTAT | 68519 |
| rs586044591 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108479011 | ATGAAAGGTTTTTTT[A/T]AAAAAAAATTATTTT | 68519 |
| rs586060283 | snp | A/G | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108369373 | AGGAGAGGGAGGAGG[A/G]GGAGGAGGAGGAGGA | 68519 |
| rs586065692 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108425251 | AATTTCACTAGGGGC[A/C]TGGGGAAGAGGGTCC | 68519 |
| rs586084941 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108527409 | CCTACAGGGCCAGAG[A/G]ACAGAGAGAGATCCG | 68519 |
| rs586085082 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108519830 | GCTGGGATTAAAGGC[A/G]TGCTCTGCCACCACC | 68519 |
| rs586102737 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108452928 | ACTTTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 68519 |
| rs586111284 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108382310 | GCACCTCTGCAAAAA[C/G]CCAGGCATGTGCCTG | 68519 |
| rs586237122 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108488641 | TCTGAGATGGTGATG[A/G]TGATGGTGATGGTGA | 68519 |
| rs586249531 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108469943 | CTATCTTTTCGTGTG[C/T]CCATTTGCCACCTGA | 68519 |
| rs586252588 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108397381 | TTCCTTCCTTCACTG[A/C]CACAGCCACAGCCAC | 68519 |
| rs586252931 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418403 | TATGAAGGGATGTTC[C/T]TTACTGGCTTGCTTC | 68519 |
| rs586254972 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489390 | AGGTGGTGAAGAAGA[A/C]GAAGAAGAAGAAGAA | 68519 |
| rs586269842 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108532683 | AGTTCCAGTACAGCC[A/G]GGGCTACACAGAAAA | 68519 |
| rs586311527 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108465127 | CTCAGAAATCTGCCT[A/G]CCTCTGCCTCCCAAG | 68519 |
| rs586317905 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442486 | AGAAAAGTGAAAAAA[A/G]TGTGCTTGCAGCTCT | 68519 |
| rs586356914 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108376467 | ATGTGGTTGCTGGGA[A/T]TTGAACTCAGGACCT | 68519 |
| rs586359298 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520312 | ACACACAGACACACA[C/G]ACACACAGACACACA | 68519 |
| rs586363181 | snp | C/T | | | upstream-variant-2KB, intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108409703 | ACACACACACACACA[C/T]ACATACCCAGTCTTT | 68519 |
| rs586377323 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108478381 | TCTTTATTCTTTATT[A/C]TTTATTATTTATTTA | 68519 |
| rs586412758 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108420568 | GGGTTCTCTGTGTAG[C/T]CCTGGCCATCCTAGA | 68519 |
| rs586449069 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471436 | GGAAGAGCAGGGGAG[A/G]AAGAGCAGGGAGTGG | 68519 |
| rs586455723 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108508575 | TTTAAAAAAAATGTT[A/C]ATACCAGACCTGGTG | 68519 |
| rs586462651 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471154 | GCACGCAATGCTGTG[A/C]GAGCTGACACAGAGG | 68519 |
| rs586478339 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108506438 | TGTTTGCTTTCGGAG[C/T]GCCCCGAGGCATGTC | 68519 |
| rs586479338 | snp | C/T | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108370221 | GAGGTCCTTTCAGTT[C/T]CCAACAACCACATGA | 68519 |
| rs586533699 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473046 | ACACATATCTCTCTC[A/T]CACACATACACCAAG | 68519 |
| rs586543424 | snp | A/G | | | upstream-variant-2KB | Eml1 | GRCm38.p3 | 12:108369396 | GAGGAGGAGGAGGAG[A/G]AGGAGGAGAACAAAG | 68519 |
| rs586550107 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108404971 | ACATGTGCACGCGTA[C/T]AACACACAAACTTCT | 68519 |
| rs586557148 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418402 | CTATGAAGGGATGTT[A/C]TTTACTGGCTTGCTT | 68519 |
| rs586572805 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474502 | TAGTTGCTGAATTTA[G/T]AAGAAAAAAACAAAA | 68519 |
| rs586579040 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461631 | GGCTTGCTCAGCCTG[C/T]TCTCTTATAGAACCA | 68519 |
| rs586585286 | snp | A/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108402034 | GTGTGTGTGTGTGTG[A/T]GTGTGTGTGTGTGTG | 68519 |
| rs586608482 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525808 | AAACCCTGTCTTGAA[A/G]CAAAACAAAACAAAA | 68519 |
| rs586615093 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525307 | AACTCAGAAATCCTC[C/T]TGCCTCTGCCTCCCA | 68519 |
| rs586624145 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523223 | AAGCTAGAAGATCCT[A/G]GGCAGATGTCATACA | 68519 |
| rs586626162 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108381008 | GTGGAGCAGGGAACA[A/G]GGAGAGGGGCGGGGA | 68519 |
| rs586628161 | snp | A/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407487 | TAGAGAGAGTCAAAT[A/G]AGATACAGAAAGACA | 68519 |
| rs586629664 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108480287 | TGTAGACTAGATCCT[C/T]TCTCTCTCTCTCTCT | 68519 |
| rs586639215 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108446565 | ACTCTAAGAAAAACC[A/G]AACCTCAAATGAAAT | 68519 |
| rs586694393 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108458957 | CAGCTACTGCACCAG[C/T]GCTATGCCTGACTGC | 68519 |
| rs586737166 | snp | A/G | | | intron-variant, synonymous-codon | Eml1, Gm33385 | GRCm38.p3 | 12:108401065 | AAAAGAGGGGGATGG[A/G]AACAGTTCCAGTTCT | 68519 |
| rs586741625 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108530204 | TTCTTGAGTAAGAGC[C/T]GAGTGGGTTTAAATG | 68519 |
| rs586745292 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108432016 | CATCAGTAGTAAAAT[A/G]TCAACATCTTTTTTT | 68519 |
| rs586794640 | snp | C/G | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108405085 | TGCCCAAGGCCAGGG[C/G]TAGGGAGCACACACA | 68519 |
| rs586809369 | snp | C/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108406475 | ACTCCTGCATTCCAC[C/T]CCACCCACCCCGCAC | 68519 |
| rs586821684 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108461692 | CAAGGGGACCTCCCC[C/G]CTTGATCTCTAATTG | 68519 |
| rs586910705 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523306 | TCAATTACCATAGAC[A/G]AAGAAACCAAGATAT | 68519 |
| rs586918766 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473124 | ACACCACATCATACA[C/T]ACACCACACCACACA | 68519 |
| rs586924525 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108389004 | CTTCATGCTTGGGTG[G/T]TAAGTACTTTATCTC | 68519 |
| rs586932527 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108426538 | TTGTTTTTTGTTTTT[G/T]GTTTTTTGAGACAGG | 68519 |
| rs586963394 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454618 | TTTCTTTCTTCCTTC[C/T]TTCTTTCTATTCATT | 68519 |
| rs586984013 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108433770 | CAGAGTATGCACTCA[A/T]GGCTCCCCAACTCCA | 68519 |
| rs587007451 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108517886 | AGAGGCAGAGGCAGA[A/G]GCAGAGGCAGAGGCA | 68519 |
| rs587062795 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523263 | AGAACACAAATGCCA[A/G]CCCAAGCTACTATAC | 68519 |
| rs587073418 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489495 | AGAGGAGGAAGAGGA[A/G]GAAGAAGAGGAAGAG | 68519 |
| rs587079277 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108473089 | TACCACACTACACAC[C/T]AAGCATACACACACA | 68519 |
| rs587083697 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108459741 | AGACAGACAGACAGA[C/T]AGACAGACAGATAGA | 68519 |
| rs587104092 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108432406 | TCTTTATCAATGGCC[A/G]TCACCTCTTCTGGGT | 68519 |
| rs587128259 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108535159 | GGAAGAAGCAGGTGA[A/G]CCCTGTGCAGAGGGA | 68519 |
| rs587140969 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108454445 | TCTCTCATCCTTTCC[A/C]TCCCTCCCTCCCTCC | 68519 |
| rs587197425 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108371490 | TAGCTTGACTCCTGG[G/T]AGCTGCAGCCTAGCG | 68519 |
| rs587208155 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108387935 | TGGTTGGTAGATGTC[G/T]GCTGAATGTTTCTGT | 68519 |
| rs587217545 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108523805 | AAAATTTACCAAGAT[A/G]AACTCTCAATTCTGA | 68519 |
| rs587233196 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108441220 | TCTTTCCACTGTTTT[A/G]GAAACAATCTGCTTC | 68519 |
| rs587235079 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108474991 | CCAAACCAAATCAAA[A/T]CAAATCAAAACAAAA | 68519 |
| rs587315548 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108489516 | AGAGGAAGAGGAGGA[A/G]GAGGAGGAAGGAGGG | 68519 |
| rs587317271 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108521993 | CAGAAGTAACAGGGA[A/C]CAGTGGGACCCAGGC | 68519 |
| rs587318935 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108485731 | CACAGAGGCACCCAC[A/T]CATTCACACACACAT | 68519 |
| rs587319888 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108525244 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 68519 |
| rs587325775 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108379381 | GCTCTTGATTTTGAA[A/C]TTGGGGTTTTGGGCC | 68519 |
| rs587326608 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108471468 | AGCAGGGGAGGGGGA[A/G]CAAGGGAGGAAGAGC | 68519 |
| rs587331487 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108455083 | GTGCATGTGTGTGTG[C/T]GCGTGTGTGTGTATG | 68519 |
| rs587332533 | snp | C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108418330 | ATTGCTGTTCATCAC[C/T]AAAGGAAGTCAGGAC | 68519 |
| rs587355551 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108468456 | TCAAACAATTTAATA[A/G]TAATAATGAAGAAGA | 68519 |
| rs587359939 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108444394 | TAGGTGTACTCAGGC[A/G]CAGGGGTTCTCATGG | 68519 |
| rs587384927 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108460352 | AAAACTTCAAAAATA[A/G]AAGCATCCCTGGTCC | 68519 |
| rs587407924 | snp | C/T | | | intron-variant, downstream-variant-500B | Eml1, Gm16596 | GRCm38.p3 | 12:108536094 | CAGATTTGCAGCCAT[C/T]TCCAGACAAACAGCT | 68519 |
| rs587430967 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108528141 | AGATACTTATATTAT[A/G]GTTCATAACCATAGC | 68519 |
| rs587431829 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108501381 | CTTCTGTTGATGGAC[A/G]TATGGCTGGTTCTAG | 68519 |
| rs587434370 | snp | A/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108475738 | GTGCCTGAGTGAGTG[A/T]GTGTGTGTGTGTGTG | 68519 |
| rs587435969 | snp | C/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108520246 | ACCCACAGACACACA[C/G]ACACACAGACACACA | 68519 |
| rs587439023 | snp | G/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108462815 | AAGGTGACACCCATA[G/T]CTGTCACATAAGGAT | 68519 |
| rs587444893 | snp | A/C | | | intron-variant | Eml1 | GRCm38.p3 | 12:108442173 | TGACCAAACGTGGGG[A/C]AATGGTAAAAATGGG | 68519 |
| rs587457958 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108373617 | TCTTTGACCCAGGTT[A/G]GGTCCTTTATTCCAG | 68519 |
| rs587461002 | snp | G/T | | | intron-variant | Eml1, Gm33385 | GRCm38.p3 | 12:108407354 | AAAAGAGGTGAGAGA[G/T]AGGAAGAAAGACAGA | 68519 |
| rs587541372 | snp | A/G | | | intron-variant | Eml1 | GRCm38.p3 | 12:108425768 | TATTCGCATATATGG[A/G]TGCATGTGAATGTAT | 68519 |
| rs864268732 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml1 | GRCm38.p3 | 12:108420477 | TCCTTCCTTCCTTCC[C/T]TCCCTCCCTCCCTCC | 68519 |
| rs864272403 | snp | A/C/T | | | intron-variant | Eml1 | GRCm38.p3 | 12:108484281 | AGGCGACCGGTAGAG[A/C/T]GGGCGTGAACTGGAG | 68519 |