| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs247272920 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84925369 | AGGCTGTGGATGCCT[G/T]TGAGTTCAAAGCCAG | 68497 |
| rs247302459 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931812 | TGAAATGAGGGACAA[A/G]GAAGAGTGTCCATCC | 68497 |
| rs247328999 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84934460 | TAATGGTCACTTCAT[A/G]TACTACAAGGCAGTT | 68497 |
| rs247329248 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84924642 | CACACTACACAGCCA[C/T]CGAGGGGCATGTGAA | 68497 |
| rs247391273 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933644 | GAAAGGAAGGGCAAA[C/T]GAATGAGGGAATTTG | 68497 |
| rs247457395 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84932480 | GAGTGGGGCTTCACA[A/C]AAAAATCTAAATACC | 68497 |
| rs247474188 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84966607 | ACACACCTTTAATCC[C/T]AGCACTTGGGAAGCA | 68497 |
| rs247502870 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947501 | AAAGCGTGTGGCCAC[C/T]ACATCCAAAGCCTAA | 68497 |
| rs247508155 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962759 | TGCTGTGTGTGTGTG[G/T]GGGGCGGGGGGTGCC | 68497 |
| rs247577889 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84956395 | ATACTCTTTCCTCAT[C/T]AGTCAGCCTCTCTGG | 68497 |
| rs247614217 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950989 | TTACTGTTCTCCAGC[C/T]GATAGACATTGTGGA | 68497 |
| rs247726710 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84961046 | GGAGAAGCATATTTC[A/C]AACTTACAAGAAACG | 68497 |
| rs247772345 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945327 | TCACATCCTGAGCCT[G/T]TAATCCTCTCCATCT | 68497 |
| rs247779112 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84934771 | GGAGGCAAAGTGTGA[C/T]GACACATGTATCACT | 68497 |
| rs247813977 | in-del | -/TTTAGG | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972209 | GTTTTTATTTTATCT[-/TTTAGG]AACAATGTCCCACTG | 68497 |
| rs247819368 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944590 | ACTGAGAGCCAGTTT[C/T]CTTCTCTGTCAAATG | 68497 |
| rs247882960 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950164 | ACTTCTGTGGCTTTA[C/T]TAGACCCCAAGGCTA | 68497 |
| rs247916898 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84962707 | GTAGGACATTACAGA[-/C]GTGGCCCATAAGGAG | 68497 |
| rs247941236 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84949561 | AGCCTGTGTTCCCCC[C/T]GTTCTCTCTTGCCAG | 68497 |
| rs247998133 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84959545 | CACTTACATCCATGC[C/T]ACCAAATACTCTTAC | 68497 |
| rs248038886 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933416 | CGATTTGTTAATACA[C/T]ATTTATCTACATTAT | 68497 |
| rs248066460 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84958723 | TGATAGCTGAGAGAG[A/C]CAGACAATTTGATTT | 68497 |
| rs248111279 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84932317 | GCTCTTTCTTCCTGT[A/C]TGAATGGTACTATGG | 68497 |
| rs248156823 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943057 | AACTTCTGTATCTAC[C/T]AACTTCACTTACCTA | 68497 |
| rs248214969 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84942614 | GGAAGGAAGGAAGGA[A/C]GGACGGACGGACGGA | 68497 |
| rs248274128 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84949406 | AGCAACCACATGGTG[C/G]CTCACAACCATCTGT | 68497 |
| rs248307159 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948281 | TTTGTACCTGAATAA[-/CT]GCAGGGCATTTCTAT | 68497 |
| rs248592134 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84946294 | CTAACTCCTTACTCC[C/T]TAAAATTGATAATTT | 68497 |
| rs248599013 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971032 | CTCAGCCTTTGGCCA[A/G]ATATAGACTCGGTGC | 68497 |
| rs248639021 | in-del | -/TTTTA | | | intron-variant | Arel1 | Mm_Celera | 12:84941357 | TTTTGTTTTGTTTTG[-/TTTTA]AGCCAGAGTCCCATA | 68497 |
| rs248663421 | snp | A/T | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969872 | TTTCTCATTCCCACA[A/T]ATTCTCCCTCTCCCA | 68497 |
| rs248688154 | in-del | -/AAA | | | intron-variant | Arel1 | Mm_Celera | 12:84960374 | AAAATAAATCTTTTT[-/AAA]AAAAAAAAAAGGAAC | 68497 |
| rs248734461 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943455 | CCCCAGGAGACAAAG[C/T]AGAGCACGTGCCGTA | 68497 |
| rs248767234 | in-del | -/CACCACCACCACCAC | | | intron-variant | Arel1 | Mm_Celera | 12:84951446 | TTTTACACACACACA[-/CACCACCACCACCAC]CACCACCAAAAAACT | 68497 |
| rs248794103 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84952671 | ATCTTCATGATAGAA[C/T]GTTATATGATAATTT | 68497 |
| rs248805909 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950627 | GCTGAGCCGTCTCTC[C/T]AGCCCCCGCATGTTC | 68497 |
| rs248986154 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947202 | AACTGTCTGTTCTTT[C/T]CTTACCTCAGATGCC | 68497 |
| rs248988146 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84968443 | GGGCTACACAGAGAA[A/G]CCCTGTCTCTAATCT | 68497 |
| rs248994283 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84937254 | AGGAAACAATCAGGA[C/T]GACCTTCAATGGATG | 68497 |
| rs249034722 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84946161 | TATATTATATAGATA[G/T]ATTTAATTAATAATG | 68497 |
| rs249070500 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84949125 | GATGCAGGGTCACAG[A/G]CAAGCTGCTTAATGC | 68497 |
| rs249102688 | in-del | -/AC | | | intron-variant | Arel1 | Mm_Celera | 12:84960149 | CTTCTGATTTCACAT[-/AC]CCCAGGCACACATTT | 68497 |
| rs249179175 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971608 | CCCATTTTATAAGTT[A/G]TAAGAATTCAGAACC | 68497 |
| rs249197234 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84926561 | CCAACCCAGAGCACC[A/G]TCTGTAGCGTTCAGG | 68497 |
| rs249200176 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84936512 | TTCGAGGAAAAAAAA[-/G]ATCTATCAAGAACCT | 68497 |
| rs249308266 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84952357 | CAGTTAACTCCCAAA[A/G]GCAGCAGACAGTCTG | 68497 |
| rs249334041 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84925637 | TGCAGAAGGTCCTAC[A/C]GGAGCAGCCTAGAGG | 68497 |
| rs249379919 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933816 | GTACCTCTGCACAGA[C/T]CATATTCATTACAAT | 68497 |
| rs249390901 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84924894 | GTCTGTTGAGAATCT[A/T]GCAGGTGAATAACCT | 68497 |
| rs249520575 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84937592 | ATGGAAAATAGAAAT[A/G]CATGAAATTCAAGAA | 68497 |
| rs249709878 | in-del | -/AAAA | | | utr-variant-5-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84951143 | CTAACTTGCACATTT[-/AAAA]GAAAAAAAAAAAAAG | 68497 |
| rs249777462 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84963503 | GCTTCCCCAAGTACA[C/G]AATGGCACGATATAA | 68497 |
| rs249782448 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84954045 | GGGAAAGCAGTACAC[A/C]TTCTTAATCACGGAG | 68497 |
| rs249846462 | snp | A/G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84953085 | AGGGCTGGCTCAGCA[A/G/T]TTAAGAGCACTGACT | 68497 |
| rs249905952 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84962801 | GAGGTCACATGTCAG[A/G]CTTCCTTGGTGGCTG | 68497 |
| rs249907580 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84952393 | AGAGTCCACATTTTT[A/C]ATGACCATTCTCCTA | 68497 |
| rs249977325 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962462 | AACTGGAGAAAGCCA[C/T]ATTCCTCAGCAGTTC | 68497 |
| rs250042980 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84965030 | TGCGCTGTGTTGCTG[A/G]CCCTCCACTCTCTTT | 68497 |
| rs250185797 | in-del | -/TT | | | intron-variant | Arel1 | Mm_Celera | 12:84961931 | ATTTATGCAGCTCTG[-/TT]TCCTGGGTTCTATAG | 68497 |
| rs250259093 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84928633 | GGGGCTGGCAAGATG[A/G]CTCAGCCAGTAAGAG | 68497 |
| rs250294522 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84951838 | TCAGCTGGAAAGAAG[C/T]GCCAGCAGAGCTTTA | 68497 |
| rs250317403 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944676 | ACGTCAGCCTAGAAC[C/T]GCAGTGAGCTTTCAG | 68497 |
| rs250359126 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961835 | CCTCAGGTCCCCTGC[C/T]GTGAAGTTACAGGTG | 68497 |
| rs250385112 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84952301 | TACAGGACTACTTAA[C/T]CAGACTTTACAGTCC | 68497 |
| rs250449298 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84951662 | CAGGCTTTCAGCAGA[C/G]GTAAGCTAGGGTACA | 68497 |
| rs250460789 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944625 | GAGTACTCACAGGCA[C/T]CTCACTTGGGTGTTA | 68497 |
| rs250522577 | in-del | -/TTGTTGTTG | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972350 | TTGATTTGGTTTGGT[-/TTGTTGTTG]TTGTTGTTGTTGTTG | 68497 |
| rs250572154 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84921857 | AAGTTGGATTATACA[C/T]TAATACAGCTGAAGA | 68497 |
| rs250596354 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972102 | GTAAACAGTTAATTT[A/G]ATGAAGACTGGGCTT | 68497 |
| rs250608701 | in-del | -/AC | | | intron-variant | Arel1 | Mm_Celera | 12:84965580 | GGTTAAAAAAAAATT[-/AC]AGTTTGACTGCAATG | 68497 |
| rs250715855 | snp | A/G | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970054 | GTAAAATACCTGCTG[A/G]CCAAGCAAGAAGCCC | 68497 |
| rs250801286 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84927274 | CAGGGTAACTTTCCA[-/C]CCCCCACGGGGAAGG | 68497 |
| rs250842488 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972450 | TGTAAACCAGACCTC[A/G]AATTTTTAGGGCTCT | 68497 |
| rs251042284 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84925944 | TGGAGAGACGGCTCA[A/G]AGGTTAAGAACACTG | 68497 |
| rs251056077 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965932 | GAAGGTCTCCATTGC[-/T]TTTTCTTCCAAATAG | 68497 |
| rs251058838 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84936637 | AAGTCTTTAGGATCC[A/G]GAATTAGCCAGAGAC | 68497 |
| rs251115234 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84951583 | TAGTTCTGCAGCTAC[G/T]TCACCAAGTCCACCA | 68497 |
| rs251115661 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945770 | TCATGGCTAGTCAAA[C/T]GATAAGAATAGTGAC | 68497 |
| rs251128476 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84951602 | CCAAGTCCACCAAGG[-/T]CCCCTGGCAATCTCT | 68497 |
| rs251222143 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960821 | CATGCTGTTGCTTAC[A/G]TCAGTAAGGAGTTTG | 68497 |
| rs251306242 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84929448 | AACTCTTACATAAAA[A/T]TTTTTTGGGTGTTTT | 68497 |
| rs251345224 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84939458 | CCACACGATGAAGGA[C/T]AGAGCTGACTTTACA | 68497 |
| rs251369147 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84938905 | GAGACTCCAATCATT[A/C]GGATTTAACTCCCAA | 68497 |
| rs251413042 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947575 | CAATGTATTCATTAA[A/G]CTCTTTAAGGCCCAA | 68497 |
| rs251544838 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931635 | GAAATACTGAAAGCC[C/G]TCAGGAAAAAAAGAA | 68497 |
| rs251568311 | in-del | -/AAAAC | | | intron-variant | Arel1 | Mm_Celera | 12:84932849 | ATAAATAAATCTTTA[-/AAAAC]AAAACAAAACAAAAG | 68497 |
| rs251607515 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942068 | TAAGAACGAAGGAGG[A/G]GAGGGAGGGAGGAAA | 68497 |
| rs251720603 | in-del | -/CCACTT | | | intron-variant | Arel1 | Mm_Celera | 12:84967760 | AAAAGTAATTACTTC[-/CCACTT]CCATTCAACACAGTC | 68497 |
| rs251725245 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84958392 | TGACTTGCCAAATAT[A/G]ACTGTGGCTTATGTC | 68497 |
| rs251784428 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84966356 | GCACATGCACATACA[A/C]AGGACAACATGTAAA | 68497 |
| rs251833225 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84953369 | TCTCATGTAGCTCAG[C/T]TGGCCTCAAAATCAC | 68497 |
| rs251841689 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965936 | GTCTCCATTGCTTTT[C/T]CTTCCAAATAGCTTG | 68497 |
| rs251842811 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84965548 | TCTAAGCAGCAAGAA[A/C]CACAGAATGAGGCCA | 68497 |
| rs251854307 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84929043 | TTTTTGGAGTGGGGT[A/G]GGGTAGGGTGGGAAG | 68497 |
| rs251960779 | snp | G/T | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84930181 | AGGTCTCTTCATATG[G/T]ACCTGCCGAAGCTCT | 68497 |
| rs252006942 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84927072 | TTTGGATAATAGCTT[A/G]ATTACTATAAGTGAG | 68497 |
| rs252031808 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84961182 | TACTCATGCTCATAG[A/C]TGATCCTCCCCTTAC | 68497 |
| rs252164696 | snp | C/T | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969721 | CCACTTCCAGGAAAG[C/T]TGTCCCTGGCCTTCC | 68497 |
| rs252266895 | in-del | -/A | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Fcf1, Arel1 | Mm_Celera | 12:84970792 | CTCCACCCGCCCCCC[-/A]AAAAAAATCTCCAGT | 68497 |
| rs252325865 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947887 | CACCTGCAGCCAGTG[A/G]GCCACATATAACTCA | 68497 |
| rs252335472 | in-del | -/ATGCAGG | | | intron-variant | Arel1 | Mm_Celera | 12:84959231 | CTGAGGAGAGGTCAT[-/ATGCAGG]AAGAAAGCAGGCAAT | 68497 |
| rs252343564 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948473 | ATCTCATGGCAAATC[C/T]TCCTGCTTTCTCCAT | 68497 |
| rs252366846 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969216 | AAGTTTCAAAATAGT[-/A]AAAAAAACACATGAA | 68497 |
| rs252380594 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947404 | TACATAGTCCTACCT[A/G]TACTGGAAACCACTA | 68497 |
| rs252382575 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84957008 | TCAATTTGCTGCCCC[A/C]ATCCCTAGAAAGCTA | 68497 |
| rs252389455 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84930901 | CCCTATGCCAGTGTT[-/C]TACAATTCAGTTTTC | 68497 |
| rs252441727 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84955772 | GCCATCTTTCTAGTC[C/T]TTAAAATGCTATTCT | 68497 |
| rs252521777 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84932156 | CCCACCGACTTGCTG[C/T]TGCTGGTTTGGTTTG | 68497 |
| rs252581781 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84927799 | AGCTTGAAGAGACTG[C/G]TCTAAGCTTTTTTGG | 68497 |
| rs252627652 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84927034 | GGATCTAACACAGAA[A/T]CCAATAGCCACAGGC | 68497 |
| rs252637512 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84938724 | TTTAATTTAAACAGA[A/G]ATGGTACATAATGAT | 68497 |
| rs252698004 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935869 | ATCTCTCAGTAGAAG[A/G]CCAGCCTAGTCTACA | 68497 |
| rs252771709 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935253 | CTTTCTGCACCAAAC[A/G]AAATGAGAAAGAACT | 68497 |
| rs252836942 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944896 | GAACTCGCATTAAAG[C/T]AAACCATCCAACAAA | 68497 |
| rs252934341 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84925446 | GACCCTGTCTCAAAA[C/T]CAAGCCAAACCAAAC | 68497 |
| rs252951012 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944054 | TTACTCAACTTGTTT[C/T]CCCCCAATTCGTACA | 68497 |
| rs252954049 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84932965 | GCAAGATTTTTTTTT[A/T]AATCTGTTATGTAAA | 68497 |
| rs252980728 | in-del | -/CT | | | intron-variant | Arel1 | Mm_Celera | 12:84923139 | GCACATGTTCTCACA[-/CT]CTGTGACACTACAGA | 68497 |
| rs252989402 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943425 | TTCAGTGTCTTCCAG[G/T]TCTCCTTAAAGCCAC | 68497 |
| rs253085039 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84934540 | AAAGGAAATGGCTAG[A/G]AAAAGACCAAGTCAC | 68497 |
| rs253180980 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964601 | AAAGCAAAACTCTGA[A/T]CCTGACAAGCCGCCT | 68497 |
| rs253239368 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84963884 | CAGGTGGCTCACCAT[C/T]CTGTACACTAGCTCC | 68497 |
| rs253293796 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84958911 | CAACAAAAAAAAAAT[-/G]ATTTTTTAAGTTATT | 68497 |
| rs253304708 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84962389 | ATCATTCTGGTGTGA[A/C]TGAGAAGATTCCAGA | 68497 |
| rs253360442 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971646 | GCGGTGGTGGCACAC[A/G]CCTTTAATCCCAGCA | 68497 |
| rs253415872 | snp | A/C | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970595 | GCCCAGGATTCCCGA[A/C]CCCTCTGCCCTCGTC | 68497 |
| rs253429535 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943249 | TATTTCTAGCTCCAT[G/T]TTCAAGGAGAAGGTG | 68497 |
| rs253443863 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84941215 | TTTTCTTTCTTGCCA[-/C]CCCCCATCCCTTTTT | 68497 |
| rs253462433 | in-del | -/TGTGTAACC | | | intron-variant | Arel1 | Mm_Celera | 12:84963170 | TGCAATTAACAGCAG[-/TGTGTAACC]TGTAGCAACTAAAAC | 68497 |
| rs253489254 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84927612 | TCTGGTCACTAAGCT[A/T]ACAGAAACACAGGTC | 68497 |
| rs253559664 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933879 | GGTTTCACATATTCA[C/T]AGAATGAAAGATCAA | 68497 |
| rs253605750 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84936974 | GTTATCACCCCTTAC[C/T]ATTTGGGAAATGCAA | 68497 |
| rs253709277 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84922240 | CTCAAGAGCCAGCAT[A/G]TTACTTAGCAGACTA | 68497 |
| rs253756069 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84924297 | CTTTCAGGGCTCACA[C/G]CACTATTCACACTCC | 68497 |
| rs253761385 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930837 | TCTGGAAGATTGAAC[C/T]GGCTCACTAGGCTTG | 68497 |
| rs253842295 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84957499 | TCATAAATGCATATA[A/G]TGTATTTTGGTCATT | 68497 |
| rs253848067 | in-del | -/GGGTGGGGGTGTAG | | | intron-variant | Arel1 | Mm_Celera | 12:84930729 | GGGTGTGGGGTGTGT[-/GGGTGGGGGTGTAG]GGGTGTGTGTGGGTA | 68497 |
| rs253867204 | snp | C/G | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84931729 | CACTCGGAAGGTGTA[C/G]AGGCGCCAGGGGATG | 68497 |
| rs253930888 | in-del | -/GA | | | intron-variant | Arel1 | Mm_Celera | 12:84946635 | AGCTTCAGGGTTAGT[-/GA]GAGATTCTATCTCAA | 68497 |
| rs253931680 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84931145 | GGGTTTGGTCTACAA[A/G]GATTTCTACCACTGA | 68497 |
| rs254055319 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84967508 | GTTTGAGACTAGAAA[-/T]AATATCTCTACATTA | 68497 |
| rs254055385 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84939521 | GCCTGGATCTGCCCC[-/T]CCCCCAATAAATAAG | 68497 |
| rs254121172 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84962595 | AAACTAAGTTTCTCA[A/G]AATCAAAACGAAGTA | 68497 |
| rs254250285 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84959280 | TTGTAGTTTCAACTA[C/T]CGTGGAGGCTGAGCT | 68497 |
| rs254369583 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84955458 | TTTTTGTTATACAAT[A/G]TATCTGAAGAAGCAA | 68497 |
| rs254429332 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964535 | CCCACAGCAGCTTCT[A/G]TGATCAGGTAGCCGT | 68497 |
| rs254432618 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84939221 | AAAGGTCTTTAAAAA[-/T]AAATCAGAAGAATGT | 68497 |
| rs254520116 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961394 | TCTATTCAAACATGT[C/T]GTCTTCTTCCTACTG | 68497 |
| rs254709914 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84941248 | GATAAGGTCACCCAG[C/T]ATAGCCCTGACCCTG | 68497 |
| rs254780667 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948848 | TCTAACTGAAGCCTT[C/T]AACTTTGTACCCGTA | 68497 |
| rs254791019 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84940564 | TCTTAGAAACACAGC[G/T]AGAGACATGTTTATA | 68497 |
| rs254798601 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945749 | TGTGGACAAGGGTAG[C/T]TATACTCATGGCTAG | 68497 |
| rs254855670 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947989 | GTTGGAAACAATGGA[C/T]AGTTCTAGAGTATGA | 68497 |
| rs255033734 | in-del | -/AC | | | utr-variant-5-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84951369 | GGCATCTGTTCTGGA[-/AC]ACCAGGATCCTCCTA | 68497 |
| rs255182830 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84933034 | GCCCCTCACATGCCT[C/T]AGACATGTTCTGCCT | 68497 |
| rs255189759 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84942756 | TCACCAGTCCTAAAC[A/G]AACCACCCAGGCAGA | 68497 |
| rs255196200 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84968604 | CTGCTCCCCTACCCA[C/T]TCAAGCCCACTTCTT | 68497 |
| rs255249852 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84932078 | GACCCTGCCTTGCCT[A/G]CTGGGGCTCAGTGAC | 68497 |
| rs255264436 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84967648 | CAAACTGTGGACTCA[A/G]GGGTCTCAGAGACTC | 68497 |
| rs255438133 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84966516 | TCAAAGGTAAAATGA[G/T]GGCCTCTGGCTATAA | 68497 |
| rs255458210 | in-del | -/AAAAAACA | | | intron-variant | Arel1 | Mm_Celera | 12:84954517 | GAGAAACCTTGTCTC[-/AAAAAACA]AAAAAACAAAAAACA | 68497 |
| rs255578497 | in-del | -/TCCC | | | intron-variant | Arel1 | Mm_Celera | 12:84933376 | ATCACCTCACTGCCG[-/TCCC]TCCCTTCTACTCTAC | 68497 |
| rs255674106 | snp | A/G | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969356 | GTCGGTCCTAGTGGT[A/G]TCTGGGTAATATAGG | 68497 |
| rs255702714 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84951973 | GGCATGGTAGTATGA[A/G]CCTGTGATCCCAGCA | 68497 |
| rs255711235 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84924753 | CATTAGTTGTGAGGT[C/T]AGTTATTTTAAGGAC | 68497 |
| rs255767971 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84951163 | AAAAAAAAAAGAAAA[A/G]AAAAAGAAAAGGCCA | 68497 |
| rs255769305 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961868 | ACGCGCCTGACAAGG[C/T]AGTGGGACGGGACCT | 68497 |
| rs255839614 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961132 | TCCGGTCGCTCTACC[A/T]CCACCAACCTTGGTA | 68497 |
| rs255852331 | in-del | -/TTTG | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972579 | TACACGTGGTTTGTT[-/TTTG]TTTTTTTTTAGCATA | 68497 |
| rs255893343 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931828 | GAAGAGTGTCCATCC[A/G]GTCTGGGTATCACAA | 68497 |
| rs255899789 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84930741 | TGTGGGTGGGGGTGT[A/G]GGGGTGTGTGTGGGT | 68497 |
| rs255902603 | in-del | -/TAA | | | intron-variant | Arel1 | Mm_Celera | 12:84931611 | AGATAACCTTTTCTT[-/TAA]TGTTCCGAAATACTG | 68497 |
| rs255961633 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84926801 | CACTTATTACAGTAA[C/T]AGAAAGCTGACTCAT | 68497 |
| rs256025856 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935803 | ATTACATGGCCAGGC[A/G]GCGGTAGCGCATGCC | 68497 |
| rs256089532 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84942990 | TTGTCCACTTGGCAA[A/T]AGCCTTCCACAAGTC | 68497 |
| rs256104356 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84965568 | AATGAGGCCACGGTT[-/A]AAAAAAAAATTACAG | 68497 |
| rs256146851 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84938554 | ATTTCTCCAGCCCCA[C/T]GTACCTTAACTGTAT | 68497 |
| rs256225015 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947154 | AGAAACTATAATAAA[C/T]ATGAATAAAGAATTG | 68497 |
| rs256315636 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84942958 | TGCTTCCCTCCACCT[A/G]GAAGCCTTTTGTTTG | 68497 |
| rs256358834 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84923557 | TCTGGCTACACAGTG[A/G]GACTGTCTCAATCCT | 68497 |
| rs256411862 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84922923 | TTTGATCCCAGCACT[C/T]GGGAGGCAGAGACAG | 68497 |
| rs256482006 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84921045 | TTGATTGCTTGGCTC[C/T]GCTTACTTCCATTCC | 68497 |
| rs256482378 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84954208 | GTTTTCTGTTTTCTC[C/T]TTTGGAGCTAAGGTC | 68497 |
| rs256555893 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84963763 | GAACTTTAGAGACAG[C/T]TGACAAGGTGCTTAA | 68497 |
| rs256559175 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84919710 | CATCAGTAGTCTTCA[A/T]GCCATCCACATGCCT | 68497 |
| rs256614101 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84966911 | AGAAGGCTGAACATG[A/G]GCAATAATTTTTCCA | 68497 |
| rs256631377 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928429 | AGGCCAGGGTAAGAT[C/T]CTGGCCTGTGAAGGG | 68497 |
| rs256673048 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84921517 | TTCAAAAAAACAAAA[-/C]AAAACAAAACAAAAA | 68497 |
| rs256789242 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84934926 | GCACCTGGAGAGCCC[A/G]ACTGTCCTGGACGGG | 68497 |
| rs256968849 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943462 | AGACAAAGCAGAGCA[C/T]GTGCCGTAAGCCTAC | 68497 |
| rs257012331 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84953039 | TTAAATAAATCTTTT[-/A]AAAATTATTTTTTTA | 68497 |
| rs257029770 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950634 | CGTCTCTCTAGCCCC[C/T]GCATGTTCACATCTT | 68497 |
| rs257101238 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945949 | CACTTTTGAACTCAT[A/G]GGAGCTATGGCTACC | 68497 |
| rs257173901 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84969399 | AGCTTAGCTTTATAC[-/A]ACAAAGAAACAGAGG | 68497 |
| rs257187340 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84953838 | AAATCCTACTGGCAT[A/G]TGCCACCACAACCGG | 68497 |
| rs257345209 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972395 | TTGTTGTTTGAGACA[A/G]GGTCTCACTAAGTAG | 68497 |
| rs257392076 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928330 | GGAAGAGAAAGAGAG[A/T]CAGAGGGATGTGGGC | 68497 |
| rs257413902 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84923664 | CACACCCTCAAGAAC[-/A]GCAGCAGTCTTGGAG | 68497 |
| rs257429789 | snp | G/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947795 | TCCTCTCTACAGTAT[G/T]CTGGCCCTTATAATG | 68497 |
| rs257459965 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84927442 | AAATTAAAAGTGATG[C/T]TGGCTTACACCACCA | 68497 |
| rs257512734 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84956838 | ATGTTCAAACAGTCA[C/T]ACACATTTTATACTT | 68497 |
| rs257531283 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84936512 | TTCGAGGAAAAAAAA[A/G]ATCTATCAAGAACCT | 68497 |
| rs257617886 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84925410 | GTATCAAATTTAAGG[A/C]GAGCCTGTGCTACAG | 68497 |
| rs257800497 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84936959 | GCACATGGAAAGATG[-/T]TTATCACCCCTTACT | 68497 |
| rs257820387 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84937178 | AGCATTTAAGAAATG[C/T]TCTTATAAAAAAACC | 68497 |
| rs257881106 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84946124 | TGGTAAAGTGCCCAT[A/G]CTCCTGCAAATATAA | 68497 |
| rs257957894 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84956423 | TGGTCCTTTAAGCAT[G/T]CCTGTGGGTCTCCTG | 68497 |
| rs257996131 | in-del | -/G | | | intron-variant | Arel1 | Mm_Celera | 12:84930796 | GGACAGCTTGTGGGT[-/G]TGGTTCTCTTCTTTC | 68497 |
| rs258011299 | in-del | -/G | | | utr-variant-5-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84951280 | AAGCATTTGAATGCT[-/G]GGGTGAAGAAATAGA | 68497 |
| rs258013989 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930290 | TTACTCTCAGGCGTG[C/T]GATGGAGCACAGCTC | 68497 |
| rs258024320 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964936 | GACCGTTTCCAGGAG[C/T]TGGTGCTCCCTCTCC | 68497 |
| rs258086572 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84953604 | TTATTTACTATTATA[C/T]ATAAGTACACTGTAG | 68497 |
| rs258091607 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964487 | CTCTTCCTTGCTTAT[C/G]CACAGGAGGAGGACA | 68497 |
| rs258092139 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948498 | CTCCATGTGGCTTCT[-/C]CCCTCCTCCTGTTCC | 68497 |
| rs258119251 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84922417 | GCTTTTCTCCCATTC[C/T]CGGATGTGTTGTCTC | 68497 |
| rs258124640 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84936733 | TACTTTCTCAATATT[-/A]AAAAAGGGTTTTACA | 68497 |
| rs258142441 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84963480 | CAAGAAATACCTGCC[C/T]AAGCAGTGCTTCCCC | 68497 |
| rs258192965 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84941963 | ATGATTCCACCTACA[C/T]GAAAGAGAAACACAA | 68497 |
| rs258202863 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962541 | GTCCACATCCCTTAA[G/T]TCTCTTTAGAGTCTC | 68497 |
| rs258349520 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84926315 | CTGCTTGTAGGCTCC[C/T]CCTAGAGAGGATTCA | 68497 |
| rs258527297 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84943796 | AATTGAAGATATTTT[A/T]TACAAGTAAATATGA | 68497 |
| rs258588479 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945613 | TCAGACCCCAGCAGA[A/G]AAGCTACAGCTATAG | 68497 |
| rs258613758 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950992 | CTGTTCTCCAGCCGA[C/T]AGACATTGTGGAAAG | 68497 |
| rs258649817 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84953005 | AATGGCATATATATA[C/T]ATACACATTAATAAA | 68497 |
| rs258710639 | in-del | -/C | | | intron-variant | Arel1 | Mm_Celera | 12:84927734 | CTAAATTCCACCATG[-/C]CAGCCAACCAGGCTC | 68497 |
| rs258727102 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84946471 | ATGGGAGCTGAACAC[A/G]GCTTAGTTGGTGCCT | 68497 |
| rs258831825 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84966169 | GAGCACAAAATGCAA[C/T]GAATATTAGCATTTT | 68497 |
| rs258844072 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962528 | AGAACCTAAGCAAGT[C/T]CACATCCCTTAAGTC | 68497 |
| rs258846571 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | Arel1 | GRCm38.p3 | 12:84947284 | AGTTTTGATTGTTGT[A/G/T]GTCCTGGAATGGACA | 68497 |
| rs258872839 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84922963 | TGAGTTCGAGGCCAG[C/T]CTGGTCTACAAAGTG | 68497 |
| rs258907320 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84955723 | AATCAAACCCAGGTC[C/T]TCCACAAGAGCAGCA | 68497 |
| rs258954984 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971127 | TAGGGAGGGGGACTG[A/G]GTGCTGTTTGGGGAG | 68497 |
| rs259098277 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84934422 | GTTTGAAATAGGAAT[C/G]AGGGGAGGGCAACCT | 68497 |
| rs259101793 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948902 | AAGTAATAGAAATAG[C/T]CAAGTATTTAGAGAA | 68497 |
| rs259123825 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930096 | CTTAGCTGCAGAACC[G/T]GCATAGGAAGACATT | 68497 |
| rs259322542 | in-del | -/GCGC | | | intron-variant | Arel1 | Mm_Celera | 12:84961789 | TGTGTGTGTGTGTGT[-/GCGC]GTGCGCATGCGCAGC | 68497 |
| rs259423350 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84921825 | TGAGTACACTAGGTA[C/G]TGAAGCAGAATCTCT | 68497 |
| rs259609472 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84931935 | GGAAGGTGAAGGTCA[A/C]TCCTGACCTGACACC | 68497 |
| rs259660884 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84942847 | CTTTCACAGACCAGT[C/T]TGCTGACCCTGTTGT | 68497 |
| rs259666149 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84931477 | CCTTTGAAAGTGGTG[A/C]TGAAGACAGAATACA | 68497 |
| rs259852223 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84961921 | ACCACCGAGTCATTT[A/C]TGCAGCTCTGTCCTG | 68497 |
| rs259884866 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84941369 | TTTGAGCCAGAGTCC[A/C]ATATAGTTTAGAATG | 68497 |
| rs259990811 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84965490 | GCTCAACACTCACAC[A/G]CACACCCAAACCCCG | 68497 |
| rs259991362 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960022 | AGGCATGGCTGGAGA[A/G]ATGATTCAGCCTTAA | 68497 |
| rs260056545 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84959163 | GCTGTAAGCCAGTAA[A/G]ACTTACAATCTTAGG | 68497 |
| rs260064742 | in-del | -/GACAGTAACAAGA | | | intron-variant | Arel1 | Mm_Celera | 12:84958549 | TCTCTCAAGGACAAT[-/GACAGTAACAAGA]GTATGCTGCTGAGAA | 68497 |
| rs260114630 | in-del | -/T | | | downstream-variant-500B | Arel1 | Mm_Celera | 12:84918075 | AGAACACATAAAGCA[-/T]TCTCTAAACGGTTTC | 68497 |
| rs260115253 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84966791 | AAACAACAACAACAA[A/C]AAAAAAAACCAGGTA | 68497 |
| rs260142002 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84924565 | GTTGGCATCAGACAC[A/T]GCAGCCCTGATACGA | 68497 |
| rs260182287 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965886 | TTGCATTTCCTTCCT[A/T]ACCAAAATGTGAAAA | 68497 |
| rs260215973 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84929283 | GACAAAACACAGACA[A/G]ACAAAACCATCTAAC | 68497 |
| rs260267797 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84968077 | AAAAACAGATTTCAA[A/G]CTTGAGAGGAAAGGG | 68497 |
| rs260325311 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84930404 | GATATTCCTTTCTTT[A/G]CAGCTGAGCTCCACT | 68497 |
| rs260363158 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947488 | AGTACTGGGATTAAA[A/G]GCGTGTGGCCACCAC | 68497 |
| rs260363182 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84940587 | GTTTATAAACATGAC[-/A]AAGAAAACCACTAAA | 68497 |
| rs260367973 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84938274 | CAGAAACAAGCCTGG[C/T]GGGGGTGGGAGAAAG | 68497 |
| rs260400080 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84922730 | CTGGCTGTCCTGGAA[C/T]TCCAGAGTGCAGGAA | 68497 |
| rs260412379 | snp | C/T | | | intron-variant, utr-variant-5-prime | Arel1 | Mm_Celera | 12:84946837 | CCATTATCATCATGG[C/T]GGGAAGCATGGCAGC | 68497 |
| rs260431658 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84926595 | CTGAGGTATGTCCTG[A/G]AAGAGAACTTCCAGG | 68497 |
| rs260445099 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931061 | GCCTCCTGTCCTGCA[A/G]TGAGTGCTGGGGCCA | 68497 |
| rs260639234 | in-del | -/TCCAGGGATCAAA | | | intron-variant | Arel1 | Mm_Celera | 12:84964961 | CTCTCCACTGTGGGT[-/TCCAGGGATCAAA]TCCAAGTTGTCAGGC | 68497 |
| rs260680639 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84966651 | CTCTGGGAGTTCCAG[A/G]CCAATCTGGTCTACA | 68497 |
| rs260728963 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965700 | CTACCAATTCTTAGA[C/T]ATGACAGATGTACCG | 68497 |
| rs260785706 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84967268 | GGCTAGAAGAAGGTG[A/T]CAAACCCCCTGGAGT | 68497 |
| rs260832767 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84959946 | CTCAGTGACCCTCCC[A/G]ACTCTGCCTCAAAGG | 68497 |
| rs260959536 | in-del | -/ATCAGAACTA | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84971380 | TGGTTTCTTAAACTG[-/ATCAGAACTA]CAGAAGTCACGATGG | 68497 |
| rs260962901 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84939217 | CTTAAAAAGGTCTTT[A/T]AAAAAAATCAGAAGA | 68497 |
| rs260994246 | snp | C/T | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | Mm_Celera | 12:84970392 | GAGACGGAGGGAGAA[C/T]ATTGGGGGGGGATGT | 68497 |
| rs261033505 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84961853 | GAAGTTACAGGTGTG[A/C]CGCGCCTGACAAGGT | 68497 |
| rs261175623 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84932556 | CAGAGGCAGGCAGAT[G/T]TCTGAGTTTGAGGCC | 68497 |
| rs261213594 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84924389 | GATGCAACAGGAAGG[C/T]ACTACGGTCTCGTGA | 68497 |
| rs261237362 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | Arel1 | Mm_Celera | 12:84943366 | GTCTCTTCAACGCCA[A/C]CGGACAGCCGAGGAT | 68497 |
| rs261270899 | in-del | -/AGAC | | | intron-variant | Arel1 | Mm_Celera | 12:84937344 | TACACTTAACAACAT[-/AGAC]AGATCGCCCGAAAAT | 68497 |
| rs261298989 | in-del | -/ACAACAAATTAATCCTTAAAG | | | downstream-variant-500B | Arel1 | Mm_Celera | 12:84917668 | TTCCTGATATAAAAA[-/ACAACAAATTAATCCTTAAAG]ACAACAAATTAATCC | 68497 |
| rs261299248 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84930746 | GTGGGGGTGTAGGGG[G/T]GTGTGTGGGTACATG | 68497 |
| rs261323715 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84933463 | GTCTCTGAGTTCAAG[A/G]CCAGCCTGGCCTACA | 68497 |
| rs261346724 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84925879 | TGAATGGAACTAACT[G/T]CTTGACACCATTTAC | 68497 |
| rs261356486 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84940930 | GATGAGAAAGCAGCC[A/G]AAAGACGAATATGGC | 68497 |
| rs261399033 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84935154 | TGAAGACCAATAAAA[A/T]GCAGATTCACAGAAT | 68497 |
| rs261600592 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960962 | ACAATGACCCTTCAG[A/G]AGTGAGTTTCTGTGT | 68497 |
| rs261707050 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84953242 | TAATAATTTTTTTTT[A/T]AAAATCAGAGGAAAA | 68497 |
| rs261743090 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962960 | ACATCCAGCTTTTTA[C/T]TCTGAGGATCTGGAC | 68497 |
| rs261770383 | snp | G/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972071 | CAACCAGTTTCTCTG[G/T]ATCGGTAAGGACTGG | 68497 |
| rs261880129 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84934233 | GGGTGAGTCTTCATC[A/G]TCCTCCTCAATAGCA | 68497 |
| rs261911311 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944091 | TCCCGCACTCAGAGA[C/T]TAGACATCTAAAGAT | 68497 |
| rs261988002 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84927243 | TCCCAGGTCAGCTGT[A/G]CGAACCTCTGTGTAT | 68497 |
| rs262019047 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84936188 | TAAGACAATTTTTAG[C/T]AAACTCTTAGGAAAA | 68497 |
| rs262064531 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945673 | ACTCCTTCTAAAGAA[C/T]GTTTACAGTCACAGG | 68497 |
| rs262157823 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84962486 | GCAGTTCAATTAAAA[C/T]TTAGCCTAATGAAGC | 68497 |
| rs262187791 | in-del | -/TAGA | | | intron-variant | Arel1 | Mm_Celera | 12:84939560 | TGGATCCTGGGTGGG[-/TAGA]TAGATAGAGAACCTG | 68497 |
| rs262302834 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964068 | TCGTTTTAACTGGCT[A/G]AGGTTTGACCTGCTT | 68497 |
| rs262372393 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84941989 | CACAAACCACATTAC[A/G]GCGACTACAGAACAG | 68497 |
| rs262408149 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84935323 | GAGGAGCACCTTCAA[C/T]CCCAGCACTCAGAAG | 68497 |
| rs262447122 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945070 | ACTGGCTTTTACATT[A/G]CCTAGACCTTTTCCA | 68497 |
| rs262499087 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931012 | CACTCCAGGATGCCT[A/G]GCCCTTGAGCTTCCA | 68497 |
| rs262538579 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84941174 | ATACTAATCTAGGAT[A/G]GCTCCTCCCACCTTT | 68497 |
| rs262576298 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Fcf1, Arel1 | Mm_Celera | 12:84970793 | CTCCACCCGCCCCCC[A/C]AAAAAATCTCCAGTG | 68497 |
| rs262681931 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84965406 | AACACTCCTCCTCCT[C/G]CTGTCCCCATCTCTC | 68497 |
| rs262708897 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972743 | GAGTTTATTAGCCTT[A/G]CTGATTAATTTTTAT | 68497 |
| rs262763636 | snp | A/G/T | | | downstream-variant-500B | Arel1 | Mm_Celera | 12:84917739 | CTGGGCAGTAGTGGC[A/G/T]CATGCCTTTAATCCC | 68497 |
| rs262803229 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965020 | TTCAACCTGATGCGC[C/T]GTGTTGCTGGCCCTC | 68497 |
| rs262946500 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84937549 | GCAGACATGGGTCAC[C/T]GTATCTGGTTTTTGT | 68497 |
| rs262949183 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964849 | AGTAACTTTAAATGC[-/T]TACTTATTTATTATT | 68497 |
| rs263039367 | in-del | -/TCTG | | | intron-variant | Arel1 | Mm_Celera | 12:84925055 | TCATGAGATAGAGTC[-/TCTG]TCTGTAGACCAGGCT | 68497 |
| rs263048641 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84946303 | TACTCCTTAAAATTG[A/C]TAATTTTCAATTTAG | 68497 |
| rs263083411 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84954498 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCTTGT | 68497 |
| rs263119759 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84925985 | CAGAGGTTCTGGGAA[C/T]AGAACCCAAATGGAG | 68497 |
| rs263217389 | in-del | -/ATATTACC | | | intron-variant | Arel1 | Mm_Celera | 12:84967131 | AACACGCTGTATCTT[-/ATATTACC]ACATTTTAAGCATCT | 68497 |
| rs263348791 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945753 | GACAAGGGTAGCTAT[A/T]CTCATGGCTAGTCAA | 68497 |
| rs263368400 | snp | G/T | | | synonymous-codon, nc-transcript-variant | Arel1 | Mm_Celera | 12:84920801 | TAAACTGAAGCAGCC[G/T]AGCCAGTTCCTCCTG | 68497 |
| rs263373634 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84953407 | CCAACCAAGGCCTTG[A/G]CCTGATGTGTACCAC | 68497 |
| rs263471378 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84947563 | ATTTGCTTGAACCAA[C/T]GTATTCATTAAGCTC | 68497 |
| rs263551160 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84942626 | GGACGGACGGACGGA[A/C]GGACACTGTAATGTG | 68497 |
| rs263584149 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84949485 | AAATTAAATAAATAA[A/T]TAATAATAAATGAAG | 68497 |
| rs263595424 | in-del | -/A | | | intron-variant | Arel1 | Mm_Celera | 12:84959657 | ATAACTGGGGGAGGG[-/A]AAAAACTGTAAAAGT | 68497 |
| rs263608416 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84949162 | TTACTTTAGCTCACA[A/G]GACTTATAAAAATGG | 68497 |
| rs263662163 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84964887 | GCGTGTGTACATAGG[C/T]ACGCATGGGCCATGG | 68497 |
| rs263675037 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84921752 | ACCACAGCACACAAT[A/T]AGCTCTGTGGCACAT | 68497 |
| rs263760202 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84928230 | CCCCTGCCTGTTACT[G/T]GTAGGGCATAGCATT | 68497 |
| rs263804845 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84923307 | AATATACTCTATAAT[C/T]CACTTAAATATGAAG | 68497 |
| rs263843114 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84931679 | AGAGCCGAGTCTGCT[C/G]AGCACAAGGTCTGCC | 68497 |
| rs263911019 | in-del | -/AAC | | | intron-variant | Arel1 | Mm_Celera | 12:84954535 | AACAAAAAAACAAAA[-/AAC]AACAACAACAACAAA | 68497 |
| rs263949404 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84964178 | ACTTCTGATCCTCAC[A/G]TCTGCCTTTACTGAG | 68497 |
| rs263994130 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84958304 | CTGTTCTAGAAGAGC[G/T]GGTCCTGAACTACAG | 68497 |
| rs264048392 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84957601 | CCCTTTCCCATGCCA[C/T]GTCTTTCTGTTGCTG | 68497 |
| rs264106068 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84950359 | TGAACCACCATGTGG[C/T]TGCTGGGATTTGAAC | 68497 |
| rs264141138 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84960665 | GAAGCATCAGACCCA[A/C]TGGAATAGGAGGAGT | 68497 |
| rs264167168 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84921401 | GTTACCTACATACAT[A/G]GGTATGCAGAATGAA | 68497 |
| rs264196732 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84929833 | GAGTGCTTCTCCAAC[C/T]ACGACTTCTGCTCCC | 68497 |
| rs264289186 | in-del | -/AAAG | | | intron-variant | Arel1 | Mm_Celera | 12:84946679 | GAAAAGCCATCAAAC[-/AAAG]ACACTTATCAACCTT | 68497 |
| rs264295594 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84922974 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 68497 |
| rs264419758 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84924787 | ATAACATTTTCTTAG[A/G]CCATAGCTAGAAGTG | 68497 |
| rs264424359 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | Mm_Celera | 12:84948341 | TAAAGACATAAAGAC[C/T]TGGTATTTTCATTCT | 68497 |
| rs264488998 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84931425 | TAGAGTGAGCTCCAG[C/T]ACACCGGAGACTATG | 68497 |
| rs264532016 | snp | G/T | | | intron-variant | Arel1 | Mm_Celera | 12:84941417 | GTACACAGGATGACC[G/T]TGAACTCCTGATCAG | 68497 |
| rs264579020 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960330 | CACACCTGTGTACTC[A/G]TGTGCACATAGCCGA | 68497 |
| rs264651016 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84965621 | GGATTGGATTCTGCA[C/T]AGAAAAGAGAAGGTG | 68497 |
| rs264701719 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84960112 | GCCATCTGTAACTCC[A/G]ATTCAAGTGTGTCTG | 68497 |
| rs264718227 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84967855 | CGTAGGCTTTAAGAT[C/T]CCCAGATTATGACAA | 68497 |
| rs264770699 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961907 | AGTAAGTGCTCTTAA[C/T]CACCGAGTCATTTAT | 68497 |
| rs264831893 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84924515 | TCTATCACCCAAGTA[C/T]ACAGATGGAAAGAGC | 68497 |
| rs264848456 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84933140 | ACTGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 68497 |
| rs264899794 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84926564 | ACCCAGAGCACCGTC[A/T]GTAGCGTTCAGGCTA | 68497 |
| rs264916191 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84935390 | CATGGTGAACTCTGG[A/G]ACAATCAGTGTTATA | 68497 |
| rs264925394 | in-del | -/CGCACC | | | intron-variant | Arel1 | Mm_Celera | 12:84965494 | ACACTCACACACACA[-/CGCACC]CCCAAACCCCGACAG | 68497 |
| rs265057549 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84942869 | CCCTGTTGTCTATCA[C/T]GAAGCCCAGGCACAA | 68497 |
| rs265074346 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84949709 | AACAAAGTGACCCAA[A/C]CTAAGAAACTCTGAT | 68497 |
| rs265109190 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84934498 | ATATCAAATGTTTGT[C/G]GGGTGGGGTGGAGAA | 68497 |
| rs265127574 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84944446 | CATAGTTCATCAGAG[A/T]ACTGACAGCTCTAAA | 68497 |
| rs265183372 | in-del | -/AAC | | | intron-variant | Arel1 | Mm_Celera | 12:84923039 | AACAAAACAAAACAA[-/AAC]AAAAAAAATGGTATT | 68497 |
| rs265197618 | snp | C/G | | | intron-variant | Arel1 | Mm_Celera | 12:84945871 | GAGAAGACCACAGAA[C/G]TTAAGAGGCAAAGAT | 68497 |
| rs265264935 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | Mm_Celera | 12:84972109 | GTTAATTTAATGAAG[A/G]CTGGGCTTCTTCGTG | 68497 |
| rs265345277 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84929560 | TATCTCCCACAAAGC[A/G]AGGCTACATAGGGAG | 68497 |
| rs265397346 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84936836 | ATAGAATTTATGTAA[A/G]GAGGCTCTCAAAACA | 68497 |
| rs265488862 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84925221 | TATCAGAGCTAATGA[A/G]GTTTAACTATCTATT | 68497 |
| rs265542436 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84918353 | CTGGTCTCCCAAGTA[C/T]CTATGTTACAAAGCA | 68497 |
| rs265611365 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84945340 | CTGTAATCCTCTCCA[C/T]CTCCCGCCCTCTCCT | 68497 |
| rs265789017 | in-del | -/T | | | intron-variant | Arel1 | Mm_Celera | 12:84957539 | TACTACCCTCTCTCA[-/T]CCCCCTCCCACTCCT | 68497 |
| rs265851896 | snp | C/T | | | intron-variant | Arel1 | Mm_Celera | 12:84956082 | CCCCATCCCAAACCA[C/T]ACCATAAAGAGCTGC | 68497 |
| rs265902987 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84963508 | CCCAAGTACAGAATG[A/G]CACGATATAATGCTG | 68497 |
| rs266000144 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84930350 | CTTCCCACCCTTACC[A/G]ATGTTCTTGTGCAAG | 68497 |
| rs266052708 | snp | A/C | | | intron-variant | Arel1 | Mm_Celera | 12:84923755 | AGGAGAGGACTAAGT[A/C]GACAAGTGGCTTTCT | 68497 |
| rs266137312 | snp | A/G | | | intron-variant | Arel1 | Mm_Celera | 12:84958987 | CATGGTGGCAGTGCC[A/G]GCTGTCCCTGCAAGT | 68497 |
| rs266209502 | snp | A/T | | | intron-variant | Arel1 | Mm_Celera | 12:84961047 | GAGAAGCATATTTCC[A/T]ACTTACAAGAAACGA | 68497 |
| rs387901856 | in-del | -/CTCT | | | intron-variant | Arel1 | Mm_Celera | 12:84967211 | TCTCTCTCTCTCTCT[-/CTCT]GTATGTGTGTGTGTG | 68497 |
| rs578342684 | snp | G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84954493 | TTCCAGGACAGCCAG[G/T]GCTATACAGAGAAAC | 68497 |
| rs578404285 | snp | A/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84932796 | GTCGCCCTCTTCTGG[A/T]GTGTCTGAAGACAGC | 68497 |
| rs578404515 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942561 | AGGAAGGGAGGGAGA[A/G]AGGGAGGAAGGAAGG | 68497 |
| rs578404911 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84922935 | ACTCGGGAGGCAGAG[A/G]CAGGCAGATTTCTGA | 68497 |
| rs578408087 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | GRCm38.p3 | 12:84971734 | TCCAGGACAGCCAGG[A/G]CTATACAGAGAAACC | 68497 |
| rs578515061 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84930329 | CACGCCCCCATGGCT[C/T]ACCGCCTTCCCACCC | 68497 |
| rs578570704 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84939736 | ACCTGAACAGTGCTC[A/G]TGAGGTCAAACAACA | 68497 |
| rs578584682 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | GRCm38.p3 | 12:84947521 | CCAAAGCCTAATACA[A/G]TTTCTAAAACATTTA | 68497 |
| rs578589338 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84962886 | CTGATAAACTGGCTG[A/G]CTGTCACCACTCCCT | 68497 |
| rs578707488 | snp | C/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84922126 | TGGGGGAGGGGGGCG[C/G]GGGGAAAGAGAGAGG | 68497 |
| rs578769706 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942441 | AGGGAGGAAGGGAGG[A/G]AGGGAGGAAGGGAGG | 68497 |
| rs578913093 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84939509 | ATGAGAACTGTGGCC[C/T]GGATCTGCCCCTCCC | 68497 |
| rs578974372 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84961603 | ACTGAACTCAGGTCC[C/T]CTGGAAAAGCAGAAA | 68497 |
| rs578995976 | snp | C/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84927773 | ACTCAGAGAAGCTGG[C/G]TCTTTGGGGGAGCTT | 68497 |
| rs579075225 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84921614 | ACACACACACACACA[A/C]ACACGATTCAGCAGA | 68497 |
| rs579087282 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942381 | AGGGAGGAAGGGAGG[A/G]AGGGAGGAAGGGAGG | 68497 |
| rs579154249 | snp | G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84968532 | ATTTTTTATTAGATA[G/T]TTTCTTCATTTACAT | 68497 |
| rs579158756 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84933148 | TCTCTGTATAGCCCT[A/G]GCTGTCCTGGAACTC | 68497 |
| rs579180237 | snp | A/C/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84955916 | TAAAAAAAAAAAAAA[A/C/G]AATGCAGTTCTCCAA | 68497 |
| rs579307339 | snp | C/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84960880 | TAATGACAGAGTAGA[C/G]GCTGCTTATCCATCA | 68497 |
| rs579346171 | snp | C/G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84950477 | TTTATTTTATACAAA[C/G/T]GAGTACACCACCATT | 68497 |
| rs579363811 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84938192 | GAAAATGTAAACGAG[A/G]AAAATACCTAAAAAA | 68497 |
| rs579513272 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956216 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 68497 |
| rs579536523 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84933613 | GGAGGAAGGAAGGAA[A/G]GGAGGGAGGAAGGAA | 68497 |
| rs579789041 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Arel1 | GRCm38.p3 | 12:84919756 | CCACGAGAGAAGCGT[A/G]CCCAGCACTGGAGGC | 68497 |
| rs579893005 | snp | G/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | GRCm38.p3 | 12:84972063 | AGAACACTCAACCAG[G/T]TTCTCTGTATCGGTA | 68497 |
| rs579912145 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84925189 | TACATAGTGATAACC[C/T]ACTGCTGCAGAGGCA | 68497 |
| rs579973109 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84933538 | CTCGGAAAAAGGAAG[A/G]AAGGAAGGAAGGAAG | 68497 |
| rs579981609 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956153 | TCTGGAGGCAGAGGC[A/G]GGCGGATTTCTGGTT | 68497 |
| rs580064898 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84930738 | GTGTGTGGGTGGGGG[C/T]GTAGGGGTGTGTGTG | 68497 |
| rs580148693 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84964889 | GTGTGTACATAGGTA[C/T]GCATGGGCCATGGCT | 68497 |
| rs580156721 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942121 | AGGGAGGAAGGGAGG[A/G]AGGGAGAAAGGGAGG | 68497 |
| rs580331820 | snp | A/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | GRCm38.p3 | 12:84971761 | AACCCTGTTTCGAAA[A/T]AAAAACAAACAAACA | 68497 |
| rs580337789 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942589 | AGGAAGGGAGGAAGG[A/G]AGGAAGGAAGGAAGG | 68497 |
| rs580346245 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956241 | CCCTGTCTTGAAAAA[A/C]AAAACAAAACAAACA | 68497 |
| rs580379251 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84923300 | CCTAAAAAATATACT[C/T]TATAATCCACTTAAA | 68497 |
| rs580477468 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84964624 | AGCCGCCTCCCTCCA[C/T]AAGTCTAGGAGTTGT | 68497 |
| rs580497743 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84931652 | CAGGAAAAAAAGAAG[A/C]CTGAGCAGCCCAGAG | 68497 |
| rs580513410 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84953561 | CTCTGCTCGCTCTGG[C/T]CCTGCTTGCTCCAGC | 68497 |
| rs580573252 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84957900 | GGGGCGGCTCACAAC[C/T]TCCTCCAGCTCCAGA | 68497 |
| rs580580114 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84940906 | ACACACAGCTACCCT[A/G]ACTATGCAGATGAGA | 68497 |
| rs580678795 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84959093 | GAACAAACAAACAAA[C/T]AAAGGGAAGTGCTGA | 68497 |
| rs580748190 | snp | A/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84937752 | AGGGATCCATCCCAT[A/T]ATCAGCTTCCAAATG | 68497 |
| rs580787558 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84945924 | TTGGCCAGACGTGGC[A/G]GGGCTGCCACACTTT | 68497 |
| rs580861917 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942235 | GAAGGAAGGAAGGGA[A/G]GAAGGGAGGAAGGGA | 68497 |
| rs580923482 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84967120 | CAAGACAGGAGAACA[A/C]GCTGTATCTTATATT | 68497 |
| rs580934536 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84932769 | GGCTCACAACCACCC[A/G]TAATGAGATCTGTCG | 68497 |
| rs580959329 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84954471 | TCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC | 68497 |
| rs581085287 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84929339 | TATTTTTCTCTCTTC[C/T]CTTCTCTTCTCTTCT | 68497 |
| rs581146827 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84957550 | CTCATCCCCCTCCCA[C/T]TCCTGCTGAATCCCC | 68497 |
| rs581197512 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84937286 | ATTGTTAAACAAATA[C/T]CCATACACTGAATGG | 68497 |
| rs581270156 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84932666 | CAAAACAAAACAAAA[C/T]AAAACGGGCTGGCGA | 68497 |
| rs581271451 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84921619 | CACACACACACACAC[A/G]ATTCAGCAGAAAACA | 68497 |
| rs581437302 | snp | C/G | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | GRCm38.p3 | 12:84970361 | AGAGAGAGAGAGAGA[C/G]AGATGCAGACAGACA | 68497 |
| rs581440699 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942393 | AGGAAGGGAGGAAGG[A/G]AGGAAGGGAGGAAGG | 68497 |
| rs581462069 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84927677 | TGGTTATTCTGTCCT[C/T]CTGGTGTGAACTGTA | 68497 |
| rs581491917 | snp | G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84960881 | AATGACAGAGTAGAG[G/T]CTGCTTATCCATCAC | 68497 |
| rs581609540 | snp | A/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84938193 | AAAATGTAAACGAGA[A/T]AAATACCTAAAAAAA | 68497 |
| rs581619616 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84946649 | TGAGAGATTCTATCT[A/C]AAAAAAATAGAGGTG | 68497 |
| rs581785872 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942365 | AGGAAGGGAGGGAGG[A/G]AGGGAGGAAGGGAGG | 68497 |
| rs581845867 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84962889 | ATAAACTGGCTGGCT[A/G]TCACCACTCCCTACC | 68497 |
| rs581854341 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84968429 | TTCCAGGACAGCCAG[A/G]GCTACACAGAGAAAC | 68497 |
| rs581969627 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84949388 | GTCCTGAGTTCAATT[C/T]CCAGCAACCACATGG | 68497 |
| rs582034558 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942557 | AGGGAGGAAGGGAGG[A/G]AGAAAGGGAGGAAGG | 68497 |
| rs582076475 | snp | G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84922663 | TTAAAGTTTCTCTTT[G/T]GTTGTTGTTTTGTTT | 68497 |
| rs582149912 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | GRCm38.p3 | 12:84971688 | GAGGCAGGCGGATTT[C/T]TGAGTTCGAAGCCTG | 68497 |
| rs582230803 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956169 | GGCGGATTTCTGGTT[C/T]GAGGCCAGCCTGGTC | 68497 |
| rs582261611 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84933555 | AGGAAGGAAGGAAGG[A/G]AGGGAGGGAGGGAGG | 68497 |
| rs582348530 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956070 | TGGATTTTTTTTCCC[C/T]ATCCCAAACCACACC | 68497 |
| rs582406485 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84961663 | CTCTCCTTTTCAATT[C/T]TTAATGGAAATTAAG | 68497 |
| rs582412469 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84939512 | AGAACTGTGGCCTGG[A/G]TCTGCCCCTCCCCCA | 68497 |
| rs582592591 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84950550 | CAGATGGTTGTGAGC[C/T]ACCATGTGGTTGCTG | 68497 |
| rs582615959 | snp | A/C | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | GRCm38.p3 | 12:84971763 | CCCTGTTTCGAAAAA[A/C]AAACAAACAAACAAA | 68497 |
| rs582629034 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84933211 | CATCCACCTGCCTCT[A/G]CCTCCCAAGTGCTGG | 68497 |
| rs582751113 | snp | A/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84930661 | TATATTTATTTATTT[A/T]GTGTGTGTGTGTGTG | 68497 |
| rs582915483 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84954494 | TCCAGGACAGCCAGG[A/G]CTATACAGAGAAACC | 68497 |
| rs582945031 | snp | A/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84922970 | GAGGCCAGCCTGGTC[A/T]ACAAAGTGAGTTCCA | 68497 |
| rs582952522 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84967217 | TCTCTCTCTCTCTGT[A/G]TGTGTGTGTGTGTAT | 68497 |
| rs582960294 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956218 | ACAGCCAGGGCTATA[C/T]AGAGAAACCCTGTCT | 68497 |
| rs582973909 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | GRCm38.p3 | 12:84971752 | ATACAGAGAAACCCT[A/G]TTTCGAAAAAAAAAC | 68497 |
| rs583030578 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84946177 | ATTTAATTAATAATG[C/T]CAATAAAAACTTTGT | 68497 |
| rs583126760 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942241 | AGGAAGGGAAGAAGG[A/G]AGGAAGGGAGGAAGG | 68497 |
| rs583158705 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84931596 | TGGCCTTTAATGAGG[A/C]GATAACCTTTTCTTT | 68497 |
| rs583205095 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84953474 | ATTTATTTATTCTAT[A/G]TATATGAGTACACTG | 68497 |
| rs583302488 | snp | A/G | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | GRCm38.p3 | 12:84972076 | AGTTTCTCTGTATCG[A/G]TAAGGACTGGGTAAA | 68497 |
| rs583363395 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84926076 | TGGATGTATCTGGTG[C/T]ACGTACATATAAGCA | 68497 |
| rs583455662 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84957888 | CCAGCACCCAGTGGG[A/G]CGGCTCACAACTTCC | 68497 |
| rs583478229 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84923384 | CTTGATAAATATTAA[C/T]GACTACTCTTCATAA | 68497 |
| rs583638683 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942137 | AGGGAGAAAGGGAGG[A/G]AGGAAGGAAGGGAGG | 68497 |
| rs583730588 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84943524 | CCTCTCTGCCACGCC[C/T]GATAGGGGCCCTGTG | 68497 |
| rs583755888 | snp | A/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84953874 | TATCTCTTTTTAAAT[A/T]TTTGAGAGAGAGAGA | 68497 |
| rs583810490 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84945918 | ATACTGTTGGCCAGA[C/T]GTGGCAGGGCTGCCA | 68497 |
| rs583815498 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956587 | AGTGGGCAATCCCCC[A/G]AATCACAGAAAGCTG | 68497 |
| rs583859655 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84933623 | AGGAAAGGAGGGAGG[A/G]AGGAAGAAAGGAAGG | 68497 |
| rs583909145 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84938188 | CATTGAAAATGTAAA[C/T]GAGAAAAATACCTAA | 68497 |
| rs583950808 | snp | C/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84931653 | AGGAAAAAAAGAAGA[C/G]TGAGCAGCCCAGAGC | 68497 |
| rs583991502 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84964658 | TTTATTAACCGCCGT[A/G]AAATGGCAGGCAAAT | 68497 |
| rs583999454 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84941994 | ACCACATTACAGCGA[C/T]TACAGAACAGACTGG | 68497 |
| rs584102806 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84959671 | GAAAAAACTGTAAAA[A/G]TAACTTACTGTGGGT | 68497 |
| rs584269140 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84950471 | GATTTATTTATTTTA[C/T]ACAAACGAGTACACC | 68497 |
| rs584297425 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | GRCm38.p3 | 12:84947304 | TGGAATGGACACCAA[A/G]GCCTTGTACATCATC | 68497 |
| rs584461677 | snp | A/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84932782 | CCGTAATGAGATCTG[A/T]CGCCCTCTTCTGGTG | 68497 |
| rs584467166 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942421 | AGGGAGGGAGGAAGG[A/G]AGGAAGGGAGGAAGG | 68497 |
| rs584577218 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84937287 | TTGTTAAACAAATAC[C/T]CATACACTGAATGGT | 68497 |
| rs584629952 | snp | C/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84927678 | GGTTATTCTGTCCTT[C/G]TGGTGTGAACTGTAG | 68497 |
| rs584698429 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84954438 | GAGGCAGAGGCAGGC[A/G]GATCTCTGAGTTCAA | 68497 |
| rs584845310 | snp | C/G | | | upstream-variant-2KB, intron-variant | Fcf1, Arel1 | GRCm38.p3 | 12:84970363 | AGAGAGAGAGAGAGA[C/G]ATGCAGACAGACAGA | 68497 |
| rs584846811 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84954514 | ACAGAGAAACCTTGT[C/T]TCAAAAAACAAAAAA | 68497 |
| rs584856675 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84932691 | TGGCGAGATTGCTCA[A/G]CGGGTAAGAGCACTG | 68497 |
| rs584950519 | snp | A/G | | | intron-variant, upstream-variant-2KB | Arel1 | GRCm38.p3 | 12:84946925 | GCCAGGAGCAGACTG[A/G]CTCCCAAGTAGCTAG | 68497 |
| rs585012843 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84960887 | AGAGTAGAGGCTGCT[C/T]ATCCATCACCAGATG | 68497 |
| rs585018325 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84939210 | GCTTTTACTTAAAAA[A/G]GTCTTTAAAAAAAAT | 68497 |
| rs585062987 | snp | G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84940763 | GTGACCAGCAGCATT[G/T]GCACTGGGGGCGGGG | 68497 |
| rs585091898 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84932821 | GACAGCTACAGTGTA[C/T]TTACATATAATAAAT | 68497 |
| rs585192274 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84968431 | CCAGGACAGCCAGGG[A/C]TACACAGAGAAACCC | 68497 |
| rs585196566 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942377 | AGGAAGGGAGGAAGG[A/G]AGGAAGGGAGGAAGG | 68497 |
| rs585267654 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84922901 | CCAGGCGGTGGTGGC[A/G]CACACCTTTGATCCC | 68497 |
| rs585332482 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84964622 | CAAGCCGCCTCCCTC[A/C]ACAAGTCTAGGAGTT | 68497 |
| rs585531258 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942560 | GAGGAAGGGAGGGAG[A/G]AAGGGAGGAAGGAAG | 68497 |
| rs585603537 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84943537 | CCCGATAGGGGCCCT[A/G]TGCCATGTGTCACAC | 68497 |
| rs585636417 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84933611 | AGGGAGGAAGGAAGG[A/G]AAGGAGGGAGGAAGG | 68497 |
| rs585639176 | snp | G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956192 | GCCTGGTCTACAAAG[G/T]GAGTTCCAGGACAGC | 68497 |
| rs585705431 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84939716 | AACATGCTACAGCAC[A/C]AGGGACCTGAACAGT | 68497 |
| rs585812948 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84953080 | AGAGGAGGGCTGGCT[C/T]AGCAGTTAAGAGCAC | 68497 |
| rs585822997 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84961799 | GTGTGTGTGCGCATG[C/T]GCAGCACCTAAGCCG | 68497 |
| rs585824383 | snp | A/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84930717 | ACAGGTATGTGTGGG[A/T]GTGGGGTGTGTGGGT | 68497 |
| rs585834955 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84931162 | ATTTCTACCACTGAG[A/C]CAACTTGCTGGCCCC | 68497 |
| rs585907301 | snp | G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84923385 | TTGATAAATATTAAT[G/T]ACTACTCTTCATAAC | 68497 |
| rs585927992 | snp | A/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | GRCm38.p3 | 12:84972035 | TTTAAAAAAAAAAAA[A/T]AAAAATAAATAAAGA | 68497 |
| rs585945030 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84933228 | CTCCCAAGTGCTGGG[A/G]TTAAGGCGTGCACCA | 68497 |
| rs585996465 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956140 | TTAATCCCAGCACTC[C/T]GGAGGCAGAGGCGGG | 68497 |
| rs586002721 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84953554 | TCAGAACCTCTGCTC[A/G]CTCTGGCCCTGCTTG | 68497 |
| rs586116693 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84950566 | ACCATGTGGTTGCTG[A/G]GAATTGAACTCAGAA | 68497 |
| rs586212049 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942341 | AGGGAGGAAGGGAGG[A/G]AGAAAGGGAGGAAGG | 68497 |
| rs586296908 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84964847 | TTAAGTAACTTTAAA[C/T]GCTACTTATTTATTA | 68497 |
| rs586301251 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942112 | AAGGAAGGAAGGGAG[A/G]AAGGGAGGGAGGGAG | 68497 |
| rs586414347 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84923283 | CTCATAGTTCACACA[C/T]CCCTAAAAAATATAC | 68497 |
| rs586478301 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fcf1, Arel1 | GRCm38.p3 | 12:84971754 | ACAGAGAAACCCTGT[C/T]TCGAAAAAAAAACAA | 68497 |
| rs586484631 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942581 | AGGAAGGAAGGAAGG[A/G]AGGAAGGAAGGAAGG | 68497 |
| rs586536194 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84931650 | CTCAGGAAAAAAAGA[A/C]GACTGAGCAGCCCAG | 68497 |
| rs586551583 | snp | G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84966805 | ACAAAAAAAACCAGG[G/T]AAAATAATATACTAT | 68497 |
| rs586582208 | snp | G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84968409 | AGCCTGGTCTACAGA[G/T]TGAGTTCCAGGACAG | 68497 |
| rs586721735 | snp | A/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84926119 | ATACACACAATACAA[A/T]TAAATCTTTAAAAAT | 68497 |
| rs586771195 | snp | C/T | | | intron-variant, upstream-variant-2KB | Arel1 | GRCm38.p3 | 12:84947004 | AGGCCACACCTACTC[C/T]AACAAGGCCACACCT | 68497 |
| rs586780854 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84945923 | GTTGGCCAGACGTGG[A/C]AGGGCTGCCACACTT | 68497 |
| rs586902687 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84932622 | GGCTATACAGAGAAA[C/T]CCTGTCTCGAAAAAA | 68497 |
| rs586952423 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84942153 | AGGAAGGAAGGGAGG[A/G]AGGAAGGAAGGAAGG | 68497 |
| rs587061134 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84932721 | GACTGCTCTTCTGAA[A/G]GTCCAGAGTTCAAAT | 68497 |
| rs587123013 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956235 | GAGAAACCCTGTCTT[A/G]AAAAACAAAACAAAA | 68497 |
| rs587126377 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84954452 | CGGATCTCTGAGTTC[A/G]AGGTCAGCCTGGTCT | 68497 |
| rs587300591 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84957524 | GTCATTTTCACCCCA[C/T]ACTACCCTCTCTCAT | 68497 |
| rs587312922 | snp | A/C | | | intron-variant | Arel1 | GRCm38.p3 | 12:84936515 | GAGGAAAAAAAAGAT[A/C]TATCAAGAACCTTGT | 68497 |
| rs587337419 | snp | A/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84953882 | TTTAAATATTTGAGA[A/G]AGAGAGAGAGAGAGA | 68497 |
| rs587430932 | snp | A/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84946358 | TATATATACAACTTT[A/T]AAAAATTTATGGCAT | 68497 |
| rs587476261 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84927602 | TCCAAGGTATTCTGG[C/T]CACTAAGCTAACAGA | 68497 |
| rs587506393 | snp | C/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84933745 | AAAAACACAAACAGT[C/T]AAAAAGCCTCTAAGA | 68497 |
| rs864281444 | snp | A/C/G | | | intron-variant | Arel1 | GRCm38.p3 | 12:84931619 | TTTTCTTTAATGTTC[A/C/G]GAAATACTGAAAGCC | 68497 |
| rs864302179 | snp | C/G/T | | | intron-variant | Arel1 | GRCm38.p3 | 12:84956156 | GGAGGCAGAGGCGGG[C/G/T]GGATTTCTGGTTTGA | 68497 |