SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3710867 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Eml6 | GRCm38.p3 | 11:30010484 | TCTTTTCTATATGTC[A/G]AGAATGGCCCACCTT | 237711 |
rs3711503 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:30010584 | TAAAGGGAAGATCCT[C/T]TGAAACATAGTCTCA | 237711 |
rs3720479 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29866027 | AATCTATAATGAAAA[A/G]GAGCAAGCTGAGCAA | 237711 |
rs3720970 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29866057 | AGTAAAACATTTTTT[A/T]AAAAAAGTACAATTT | 237711 |
rs3722277 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29866307 | ATTAGAGGCCAGCTT[A/G]GTCTACAGAGAAAGT | 237711 |
rs3722907 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29866427 | CTCATCAAGTAGCAG[A/G]ATTTGGCAGCTTCAG | 237711 |
rs3723433 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29770526 | GCAGTCTGTTTTAGG[C/T]TGCCATGACACTGTT | 237711 |
rs3724126 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29770647 | AGAAACAATTCACAG[C/T]GTAAAATTTATTCCT | 237711 |
rs3724130 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29770650 | AACAATTCACAGTGT[A/G]AAATTTATTCCTCAG | 237711 |
rs6162931 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29882764 | CATTTTAAAGTATGT[A/G]CATATATTTTACAAA | 237711 |
rs6162996 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29882804 | AGGCTGGTTGGTGGA[A/G]TTGGTTAGAGCATAG | 237711 |
rs6163412 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29882846 | ATAATTCCTTTTTAA[C/T]CAAAATATTATAGTT | 237711 |
rs6165034 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29883184 | GGAGCACAGGTTCAG[A/T]CAGATTCTGCTACTC | 237711 |
rs6286383 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29862743 | TGCCACCCCCTTCTT[C/T]CCTTGATGGGCAGCT | 237711 |
rs6286818 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29862798 | TTTATTATCTTAATG[A/T]GCTAGCATTGTGAAC | 237711 |
rs6286875 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29862833 | AGAAAGCAGAGTGGT[A/G]GATTAGCACAGAAAA | 237711 |
rs6287858 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29862952 | CACATGGCAAAGAGC[A/G]CAGGGCACCCTTCCC | 237711 |
rs6288438 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29863078 | CATGGGCAGTGGTAG[A/G]TGGGTTGAACACTAA | 237711 |
rs6288475 | snp | A/G/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29863097 | GTTGAACACTAAGAC[A/G/T]GAAAAACATTGCCTC | 237711 |
rs6310062 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29801709 | AAGATTCTGAACTTT[A/G]TACATGCATTATCAA | 237711 |
rs6310518 | snp | G/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29801756 | AGACTGTAGACATTG[G/T]TTTTACACGTGGCTG | 237711 |
rs6310524 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29801764 | GACATTGTTTTTACA[C/T]GTGGCTGGGATATTT | 237711 |
rs6311079 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29801866 | CATAACCACCTCCTC[C/T]TGAGTGTGGCATGAC | 237711 |
rs6339303 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872102 | tggggaatcactgga[A/G]ggttttgaaaaaaga | 237711 |
rs6339752 | snp | G/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872154 | ACACAAAACAATTTT[G/T]AAAGCTGCTGGACAC | 237711 |
rs6339814 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872200 | TGTTGAAATCCATGT[A/G]CTCCATGATGCTCCA | 237711 |
rs6340315 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872249 | AAACCTTGTGTCCCG[C/T]AGAGCCCAGCCCCAG | 237711 |
rs6340901 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872402 | TCTAGTCCTTTGGCA[C/T]ACATCTCAACAGATG | 237711 |
rs6341293 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872447 | ATTGAATGGGAAAAT[A/G]ATAGATCTTGCATTG | 237711 |
rs6341435 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872535 | TTGGTTGACACTTTT[A/T]AAGAAATTNTTTTTA | 237711 |
rs6341800 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872544 | ACTTTTNAAGAAATT[A/G]TTTTTACCTTTTCTT | 237711 |
rs6341954 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872631 | CAATTTGCTTTAAAA[A/T]GTTGGANGCAACATA | 237711 |
rs6341967 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29872638 | CTTTAAAANGTTGGA[C/T]GCAACATATGCTGTT | 237711 |
rs6352018 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29855853 | ATACCAGTCCAGGCT[A/G]CTATAACCAGCAAAA | 237711 |
rs6363833 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29765278 | CTTAGTTTAGAGTGT[A/G]CTGGGGAGGGACTCA | 237711 |
rs6366634 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29805253 | GAAAGGAACAAGGGG[A/G]TTGATTTATTACCCT | 237711 |
rs6366665 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29805272 | ATTTATTACCCTAGA[A/G]AGCTGAAGCTTCCCA | 237711 |
rs6367196 | snp | A/C | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29805354 | GTCAAAGTAACAAAA[A/C]CAGCAAGGGCATCAT | 237711 |
rs6367302 | snp | C/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29805408 | GTATCTATGACATTC[C/G]TACTTGCTGTCAAAT | 237711 |
rs6380698 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29805558 | TCCTCACTCTTGGCA[A/T]CATAGAGTCTAACAG | 237711 |
rs6380736 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29805580 | GTCTAACAGAGACTT[A/T]TCCATTAAATAGTCC | 237711 |
rs13480936 | snp | C/T | 0.497041 | 0.0383476 | synonymous-codon | Eml6 | GRCm38.p3 | 11:29749331 | TTTGCAGTAGCCGAT[C/T]CGGTTCAGACTTGTG | 237711 |
rs26821535 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30027006 | GACACTACTAAACAT[C/T]AAAACATGGCTTAGA | 237711 |
rs26821536 | snp | A/T | 0.18 | 0.24 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026496 | TCCCCTATTATTCCA[A/T]AGGATTCTGATTTAT | 237711 |
rs26821537 | snp | A/C | 0.48 | 0.0979796 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026459 | TTGCAGCACTTGACT[A/C]ACGCTGTTTCCTACT | 237711 |
rs26821538 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026397 | TTTCCTCAGGACTTT[C/T]ACTTGCGCCAGTCCC | 237711 |
rs26821539 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026322 | CATGGTGACCCAGGC[C/T]AGCGGCATGCGCGTC | 237711 |
rs26821540 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026191 | TGAGGCGAGCGCCTC[G/T]AGTGTACTACAAGTC | 237711 |
rs26821541 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026090 | GTTCGGAAACGCAGA[C/T]GCCTCCTAGGGCCGA | 237711 |
rs26821542 | snp | C/G | 0.48 | 0.0979796 | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026072 | CGCGGCGAAATTGCG[C/G]CGGTTCGGAAACGCA | 237711 |
rs26821543 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:30025519 | TCATAATTTTTTTTT[C/T]TCTGAATCGGAGGAA | 237711 |
rs26821544 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Eml6 | Mm_Celera | 11:30025422 | TCCAAACCCTCTATG[A/C]GCCTTCTCTTCACAG | 237711 |
rs26821545 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Eml6 | Mm_Celera | 11:30025265 | CCACCTTAATTATAG[A/G]AAATACTCCCTAAAC | 237711 |
rs26821546 | snp | A/G | 0.408163 | 0.193609 | utr-variant-5-prime | Eml6 | GRCm38.p3 | 11:30024999 | GCTTCGCAGCAGGCG[A/G]TGGGATTTATTCTGT | 237711 |
rs26821547 | snp | A/G | 0.459184 | 0.136902 | utr-variant-5-prime | Eml6 | Mm_Celera | 11:30024851 | GGTACCAGTACCCGC[A/G]CACACGCCTCACTGC | 237711 |
rs26821548 | snp | A/G | 0.408163 | 0.193609 | utr-variant-5-prime | Eml6 | Mm_Celera | 11:30024593 | ATAAGCCGACACCGC[A/G]CGACCCCCGGGTGCC | 237711 |
rs26821549 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:30023894 | TGCCTTAGGTCCAAC[A/G]CATATGGGATGAAGA | 237711 |
rs26821550 | snp | G/T | 0.375 | 0.216506 | intron-variant | Eml6 | GRCm38.p3 | 11:30013270 | TCTTCTGACGTCTCT[G/T]TAACTTGTTTTAATC | 237711 |
rs26821551 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:30011986 | CAGTTTCTCCAAATG[C/T]AAATGGCTCCTTTCT | 237711 |
rs26821552 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:30011952 | AAATCTATTGTCTTG[A/G]CTGCAGCTTGCTCTA | 237711 |
rs26821553 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:30011875 | GACTCAATAGACTCA[C/T]CTCCAGCAACAGAGC | 237711 |
rs26821554 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Eml6 | GRCm38.p3 | 11:30011785 | ACAACAAAACAACCA[A/G]TGGGGAATAGGAAGA | 237711 |
rs26821555 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:30011219 | CCAAGCTACAAACAA[A/G]ATGACTCAACCCTCA | 237711 |
rs26821556 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:30010386 | CCATAACATACCACT[C/T]GTCTTTTGAATTTAA | 237711 |
rs26821557 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:30010363 | TCCTCTTCTGGGGAC[A/T]GAAAACTCCATAACA | 237711 |
rs26821558 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Eml6 | Mm_Celera | 11:30010282 | CATCGGCAGAGTACA[A/C]AGAGGCATGTCAAGC | 237711 |
rs26821559 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Eml6 | GRCm38.p3 | 11:30010170 | TGCACTGTGGTCTCA[C/T]GCCTGGAGAAAGGAA | 237711 |
rs26821560 | snp | A/G/T | 0.426035 | 0.177515 | intron-variant | Eml6 | GRCm38.p3 | 11:30010120 | AAGAAGTCAATGAAC[A/G/T]CAATATAATACAATG | 237711 |
rs26821561 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30010017 | AGAGGAAGAAATCAA[A/G]GGGCAAATAAAAATA | 237711 |
rs26821562 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30008630 | TCCCTGCCTGTCAAA[C/T]AGTCCTTCATCCTTC | 237711 |
rs26821563 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:30008492 | ATCCCCAACCCCACT[C/T]TCTTTCAGCTTCATG | 237711 |
rs26821564 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml6 | Mm_Celera | 11:30008339 | TTTAATATCAGAGGA[A/G]TAAGTAAATTAGAGG | 237711 |
rs26821565 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30008229 | ATCCCCATGGACAAT[A/G]CTATTCTCTCTCTTT | 237711 |
rs26821566 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30008166 | TTTAACTGAGGCCCA[A/G]AACAGTCACAGGCTT | 237711 |
rs26821567 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Eml6 | Mm_Celera | 11:30008115 | CCAAAAACCTCAGTA[A/G]GAACTTTAGAAAGTC | 237711 |
rs26821568 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30008020 | ACTGGAGCAATTTCA[C/T]AGGAATCCCTGTGGC | 237711 |
rs26821569 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30007411 | ATGCCCCTGATTTAT[A/G]TCCTACCATCGTGAA | 237711 |
rs26821570 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Eml6 | Mm_Celera | 11:30007322 | GCTGGTTTTCCAGGC[G/T]TTCTTTATCCTCCTC | 237711 |
rs26821571 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30007221 | AACCTTTAAAAGCCA[G/T]ATGCAAGTACAAGCC | 237711 |
rs26821572 | snp | A/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:30007213 | TATAATGGAACCTTT[A/T]AAAGCCATATGCAAG | 237711 |
rs26821573 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | GRCm38.p3 | 11:30007135 | AGCATGCAACCCACC[A/G]GAGCATAAGCAGCAT | 237711 |
rs26821574 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30007087 | GGCTGTGGATGGAAG[C/T]CATTAAGCCTAGATC | 237711 |
rs26821575 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30007056 | CTTCTCTTATTTTCC[A/G]GGAGAGGAACAAGTT | 237711 |
rs26821576 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:30007030 | TCACAGAGAAGCAAT[A/G]TCTGTCACAGCTTCT | 237711 |
rs26821577 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Eml6 | Mm_Celera | 11:30006988 | GACTGTATTCTATCA[C/T]GCAGCACAGCAGACC | 237711 |
rs26821578 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30006930 | TGACTTAGGAAATCA[C/T]TGTGAGCAGGCCAAG | 237711 |
rs26821579 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Eml6 | Mm_Celera | 11:30006601 | TTTTCTCCTATAGAT[G/T]ACACAGTTTGTACAA | 237711 |
rs26821580 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30006458 | AAGCTGTAGGTCAGG[A/G]CAAGATGGTCTATAC | 237711 |
rs26821581 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:30006352 | TAGGTTTTAAGCAGG[A/G]ACTAAGACTGAAACG | 237711 |
rs26821582 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:30003622 | GAACTTGCAGCTTGT[C/T]AGTTTTGAGTCTAAG | 237711 |
rs26821583 | snp | A/C | 0.32 | 0.24 | intron-variant | Eml6 | Mm_Celera | 11:30003502 | GGTTTTTCTTTGAGC[A/C]TGTCCTAAGCACTGA | 237711 |
rs26821584 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:30003374 | TTGCACATGTCCAGT[G/T]CTTGTGACTGGCATG | 237711 |
rs26821585 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29996500 | GTATTCATTCCCACA[C/T]TATCAAATTGAGCTG | 237711 |
rs26821586 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:29996468 | TCATACCCGGAGCCA[A/G]CCAGGATTGCTGATT | 237711 |
rs26821587 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:29996224 | CCTTATCTTGAGTGG[C/T]TCAGTGAAAGTGGCA | 237711 |
rs26821588 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Eml6 | Mm_Celera | 11:29996175 | CCAGGAACTAAAACA[A/G]TCAAAATCATCAAGT | 237711 |
rs26821589 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Eml6 | Mm_Celera | 11:29996026 | AGATGGTCCCATGAT[A/G]ACAACAGGAGCCAGA | 237711 |
rs26821590 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:29995491 | TGCGCACAGCACTCT[A/C]CAGAAAGATCGGAAC | 237711 |
rs26821591 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29995458 | TCTGCTATGGGCATC[C/T]AGGCTGTCCTCTCCA | 237711 |
rs26821592 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29995268 | TCCTGGTTTCATCTG[C/T]TAACTGAGCTCCTTT | 237711 |
rs26821593 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:29995169 | TTTTTCTGGGTAAGA[A/G]CGGCTGTTTTCTTTG | 237711 |
rs26821594 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Eml6 | Mm_Celera | 11:29994961 | AAGCTGAGATTTACA[C/T]GACTTTATTGTTTTC | 237711 |
rs26821595 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Eml6 | Mm_Celera | 11:29994761 | CCCTGCCAGCACGGA[G/T]CCTGACACACATGGG | 237711 |
rs26821596 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Eml6 | Mm_Celera | 11:29994690 | CTGCTAGAACAGTGC[A/G]TAAGTGTGAAGCGTG | 237711 |
rs26821597 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:29994572 | TGGAGGGCTGGTGGC[A/T]GAGCGTCAACTGTGC | 237711 |
rs26821598 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29994549 | GGAGCAGGTATGTCT[A/G]CTGTGCTTGGAGGGC | 237711 |
rs26821599 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:29994060 | CATCAGATTTCTTGA[A/G]GCAGAATCAATATCT | 237711 |
rs26821600 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Eml6 | Mm_Celera | 11:29992047 | TGGGTTCTGATGTGC[A/T]AGCCCTGGAACTACT | 237711 |
rs26821601 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29986215 | TGTTATACGATGGAA[A/G]GTCAAGAATAGGAGA | 237711 |
rs26821602 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml6 | GRCm38.p3 | 11:29984223 | CCACTATGCAACTGT[C/T]CTTCTGTGCTCAGAA | 237711 |
rs26821603 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Eml6 | GRCm38.p3 | 11:29983093 | ACACACTCAAGGGTG[A/T]AAGGCAGCCAAAGCA | 237711 |
rs26821604 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29982148 | ACAGCAGAGTGCATT[G/T]TGTACTCCAGGAGGA | 237711 |
rs26821605 | snp | A/C/T | 0.35503 | 0.226867 | intron-variant | Eml6 | GRCm38.p3 | 11:29972065 | GGCCATGGACAGGTT[A/C/T]CTTAACTCTGAGCCA | 237711 |
rs26821606 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:29971748 | TATGCATGTGGAGTG[C/T]CCTCAAGGTTTTGTG | 237711 |
rs26821607 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29954077 | CCAGCACATAAAGGG[A/G]CTGACAGAATTTGCA | 237711 |
rs26821608 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29953610 | GTAACTACAGGACAA[A/G]GCTAATGGTCACTGA | 237711 |
rs26821609 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29953466 | AGCGATACGGTCAGA[A/G]AAGGGCATTTCCCAG | 237711 |
rs26821610 | snp | C/T | 0.18 | 0.24 | intron-variant | Eml6 | Mm_Celera | 11:29953354 | TCTTGCAATATAATA[C/T]AGGATTTTGTTATAT | 237711 |
rs26821611 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Eml6 | Mm_Celera | 11:29952456 | CCTTGGAAACATGGA[A/T]CTATGTAGAAATGGT | 237711 |
rs26821612 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29951886 | CCAAGCTACCTTACA[C/T]GCTGAAGACAAGAAT | 237711 |
rs26821613 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29948296 | GGCTTAAAGTGTAGC[G/T]ACTGTGAAGAGCATG | 237711 |
rs26821614 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:29947372 | AGCAGGAACCACACA[C/T]GACCTAGTTCATTTC | 237711 |
rs26821615 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:29946949 | GCAGCACACAGAGAG[A/G]ATGTTAGTATGAGAT | 237711 |
rs26821616 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Eml6 | Mm_Celera | 11:29943881 | TTGATTTTGGTTTAC[A/G]GTTTGCTCTTTTGTC | 237711 |
rs26821617 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:29943302 | AAATATTCACAACCC[A/G]AAACAATATTTTTTG | 237711 |
rs26821618 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Eml6 | GRCm38.p3 | 11:29943283 | ACAAATACCTACCAC[C/T]GAGAAATATTCACAA | 237711 |
rs26821619 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Eml6 | Mm_Celera | 11:29938461 | TTCTGGCACATCCAG[A/G]ATCACGGGATCATAG | 237711 |
rs26821620 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Eml6 | GRCm38.p3 | 11:29938008 | ATGATCACAATAATC[G/T]TTTGCCTTCCTTGAA | 237711 |
rs26821621 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29936766 | ACATTTACGATTGAC[C/T]TAGAGGAAAGGGGGC | 237711 |
rs26821622 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Eml6 | GRCm38.p3 | 11:29936743 | AAGTCAATCCCTGAG[C/T]TCACTTCACATTTAC | 237711 |
rs26821623 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Eml6 | GRCm38.p3 | 11:29936560 | CTCCAGAGAACATCA[A/G]CATCCTGAGAATAGT | 237711 |
rs26821624 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Eml6 | Mm_Celera | 11:29936557 | CTTCTCCAGAGAACA[G/T]CAGCATCCTGAGAAT | 237711 |
rs26821625 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Eml6 | GRCm38.p3 | 11:29936095 | TGCATCAGTGTTCCA[A/C]GGTCTAGATAGTCAT | 237711 |
rs26821626 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Eml6 | Mm_Celera | 11:29935974 | GGTAAGTATGCTCAT[A/G]AAGCAGAAATCATGC | 237711 |
rs26821627 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml6 | GRCm38.p3 | 11:29935141 | AAAAACCAAGTATGT[A/G]CATGAGCGCATAATA | 237711 |
rs26821628 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Eml6 | Mm_Celera | 11:29934455 | AGAATATGAGATTCC[C/T]TTGAATTACACCCAT | 237711 |
rs26821629 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Eml6 | Mm_Celera | 11:29933850 | GAAACCTTTGGCCTT[A/G]CAGCTGGTGTGAATC | 237711 |
rs26821630 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Eml6 | Mm_Celera | 11:29933685 | TGCTGGGAGAGTGAC[A/G]CATCCTGGCGCAAGA | 237711 |
rs26821631 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Eml6 | GRCm38.p3 | 11:29933681 | CTGATGCTGGGAGAG[A/T]GACACATCCTGGCGC | 237711 |
rs26821632 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Eml6 | GRCm38.p3 | 11:29932568 | GATGGGGACAACAAG[C/G]ACCAGTTAGCCAAGG | 237711 |
rs26821633 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Eml6 | GRCm38.p3 | 11:29932402 | AGAGTGTGCCCTACA[A/T]GATGGTCTCTCTGGC | 237711 |
rs26821634 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29931992 | CCTCAAGCTGCGATC[A/G]AATGGGCGAGCGAGA | 237711 |
rs26821635 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29931932 | TTTTTGAGTGTGGGC[A/G]TTCAAGCAAAGCAGA | 237711 |
rs26821636 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Eml6 | Mm_Celera | 11:29931394 | ATGCAAGTAGCTGGA[C/T]TTGGCGTTCTGAGCT | 237711 |
rs26821637 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Eml6 | Mm_Celera | 11:29931326 | CTTGATTCTTTCTGG[C/T]CACTGCCTGGCAGCT | 237711 |
rs26821638 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | GRCm38.p3 | 11:29930962 | GAGGCATGGGGCACA[A/G]CACAGCACTGTCCTA | 237711 |
rs26821639 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29930905 | CTCCTTCTTCTCTGG[C/T]GAATTCTGTGAAACT | 237711 |
rs26821640 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml6 | GRCm38.p3 | 11:29930803 | CTTAGTCCTGGACAA[C/T]AGCTGTATAGATTTC | 237711 |
rs26821641 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Eml6 | GRCm38.p3 | 11:29930722 | CCTGCAGTAGGCCAG[A/G]ATGGAGACATGTCAA | 237711 |
rs26821642 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Eml6 | GRCm38.p3 | 11:29929598 | TGCAAAATGATAAGG[A/G]TGCTGCTCAGATTCA | 237711 |
rs26821643 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Eml6 | Mm_Celera | 11:29929099 | AATTAAGTGTTAATA[C/T]TCGGACTATATTTTA | 237711 |
rs26821644 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Eml6 | Mm_Celera | 11:29929004 | TTATGTGGATTGGCC[A/T]GGAATTATCTATTAA | 237711 |
rs26821645 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Eml6 | Mm_Celera | 11:29928645 | GGTTTTGAAACCTGC[C/T]TCTGAATTCTTGGGC | 237711 |
rs26821646 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Eml6 | Mm_Celera | 11:29928582 | CAAGGAAGGCCATAT[A/G]ACATGACAGTCAAAG | 237711 |
rs26821647 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Eml6 | Mm_Celera | 11:29926438 | TTTGTTCCACTGCAG[A/G]GAGAAGCAGTTATTA | 237711 |
rs26821648 | snp | A/C/G | 0.297521 | 0.245442 | intron-variant | Eml6 | GRCm38.p3 | 11:29926277 | TGAGTCTGTTCCCTC[A/C/G]CCGCAGGCTTCCAAC | 237711 |
rs26821649 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Eml6 | Mm_Celera | 11:29925852 | AACAAGATGAGCTTG[C/T]AGCCCTACCTTTTCC | 237711 |
rs26821650 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml6 | Mm_Celera | 11:29925811 | TATTGCTCCAACACT[A/G]AACTACATTGAGTTT | 237711 |
rs26821651 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Eml6 | GRCm38.p3 | 11:29925809 | GGTATTGCTCCAACA[C/T]TGAACTACATTGAGT | 237711 |
rs26821652 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Eml6 | Mm_Celera | 11:29925195 | ACAACAACAAAAAAG[C/T]TAATCACAATAGTTC | 237711 |
rs26821653 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29924771 | ATCATGAGTGTCCAG[C/G]AATCCAAAGAGACCT | 237711 |
rs26821654 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Eml6 | Mm_Celera | 11:29924742 | TGTGGTATACATTCC[A/C]AACTGAGCATGAGAT | 237711 |
rs26821655 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Eml6 | Mm_Celera | 11:29924445 | TAAGCAAAAGCATGA[C/G]TCAAGCACGCAGGGT | 237711 |
rs26821656 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Eml6 | Mm_Celera | 11:29924103 | TGGAAAGGGTAATGT[A/G]GGATTCTGTGTCTAT | 237711 |
rs26821657 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29924020 | AACAGATGGTTTGGA[G/T]GCTTGGAGGTAAGAG | 237711 |
rs26821658 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Eml6 | GRCm38.p3 | 11:29923991 | CTATGTCTAAGGCAA[C/T]CAGAAGCTGTATTAA | 237711 |
rs26821659 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Eml6 | Mm_Celera | 11:29917224 | CAGCTCTCACCATAA[A/G]CAACTGTTTTTCAAG | 237711 |
rs26821660 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29916837 | GACATGGCACGATGT[A/G]GCAAGCACAGGGTCT | 237711 |
rs26821661 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Eml6 | Mm_Celera | 11:29916026 | TTTAGAGAGAGAATG[G/T]TATCTTCAGTTGTGT | 237711 |
rs26821662 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29915836 | TATAAAGTCAAAGTC[C/T]TCTCCTTTCTTTATA | 237711 |
rs26821663 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Eml6 | Mm_Celera | 11:29915810 | CCTAATGACAAAGCT[C/G]TAACGTTGGATATAA | 237711 |
rs26821664 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Eml6 | Mm_Celera | 11:29915767 | AGACCTGAACATCAG[A/G]TTGGATGGAAATTTG | 237711 |
rs26821665 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29914393 | TGATAAATGCTACAT[C/T]CAACGAGAATACATG | 237711 |
rs26821666 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29914337 | GTACTCTCTAATCCA[C/T]GGTAGAGCGGAGTCT | 237711 |
rs26821667 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29910030 | ATGGGGAGTTGCCAA[C/G]GCCCAGTGGAGGCAT | 237711 |
rs26843868 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29909939 | ACCCAGAGTGCTTGG[C/T]GCTTCTCTCAGTGAT | 237711 |
rs26843869 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:29909761 | CTTGCTTATCAGGTT[A/G]GACAAAGCCCCCTAA | 237711 |
rs26843870 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29909739 | ACAGGGCCATGGAAA[G/T]AGAAGCCTTGCTTAT | 237711 |
rs26843871 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:29909152 | TCGAGCCACAGCTTG[A/T]CTCCTCACTCACCAC | 237711 |
rs26843872 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29909097 | ATCTTCACACAAGGA[A/C]ATCATCCCAACATAA | 237711 |
rs26843873 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29909033 | TACTGTGTAATGACC[C/T]ACTGTGATGAAAGGT | 237711 |
rs26843874 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Eml6 | GRCm38.p3 | 11:29908106 | ATACATTTAAGAACT[C/T]CAAGGAGAACCATTT | 237711 |
rs26843875 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:29907520 | CTCCTTCCCCAGCTT[A/G]CACACAACATGTGCT | 237711 |
rs26843876 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Eml6 | Mm_Celera | 11:29907312 | CTCAGATGTTCTCTT[A/G]TGCCCACACATTTAT | 237711 |
rs26843877 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Eml6 | Mm_Celera | 11:29907273 | TGTTTGAATATATGG[G/T]GCCTTTACTGTAGGG | 237711 |
rs26843878 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:29907099 | GGCCTGGTAAGCATG[A/G]ACTGAAATCTTCAAA | 237711 |
rs26843879 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29907022 | AGGCTTGTCTTTTCT[C/T]TGGTATTTTCCTCTA | 237711 |
rs26843880 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Eml6 | Mm_Celera | 11:29906986 | CCTGGGACTGGGAAG[C/T]AGTTGGAGGAAGGTC | 237711 |
rs26843881 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Eml6 | Mm_Celera | 11:29906855 | TGAAGGATTGGTTCC[C/T]AATACAGCAAGGTGT | 237711 |
rs26843882 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:29906781 | TTGGAAGAAAAGGCT[A/G]TGAACAACCTTTAAA | 237711 |
rs26843883 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Eml6 | Mm_Celera | 11:29906780 | ATTGGAAGAAAAGGC[C/T]GTGAACAACCTTTAA | 237711 |
rs26843884 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Eml6 | Mm_Celera | 11:29906168 | AAATTAGAAAGATAC[A/G]TACCTGTCCATCCGA | 237711 |
rs26843885 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Eml6 | Mm_Celera | 11:29906025 | TGAGAGTGATGAACC[A/G]ACACCACTAGCCTGA | 237711 |
rs26843886 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29905848 | CCAGGATGTGAGGGC[C/T]GTGCAAATGACTTGG | 237711 |
rs26843887 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Eml6 | Mm_Celera | 11:29905601 | ATTATACATGGCTCT[A/G]ACTTGGAGTGTAAAG | 237711 |
rs26843888 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29905575 | ATTAATTTGGACAAT[A/G]TTTAAATAACATTAT | 237711 |
rs26843889 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Eml6 | GRCm38.p3 | 11:29905303 | CTTTGACATTTTCAG[C/T]TAGTGAAATTAATTA | 237711 |
rs26843890 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:29905134 | ATGAGGATTGGAGCA[C/T]GGCCCAGGGTATGCA | 237711 |
rs26843891 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml6 | Mm_Celera | 11:29905102 | AGAGGACAAAGCAGG[C/T]AAATAGCAAACTTCA | 237711 |
rs26843892 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Eml6 | GRCm38.p3 | 11:29904927 | AGCTGTAAGCTTAGC[A/G]ACATGTGAATGAAGC | 237711 |
rs26843893 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29904654 | CACAACACGCTCTCT[C/T]ACAACAGCAGAAGAT | 237711 |
rs26843894 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29904593 | GCCATTCTCACTGTC[A/C]ATAACTCATCCAGTT | 237711 |
rs26843895 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Eml6 | GRCm38.p3 | 11:29904567 | AGTGGGCATGTCCGC[C/T]TACATCTGTGGCCAT | 237711 |
rs26843896 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Eml6 | Mm_Celera | 11:29904491 | GTTTGTGATACTGTA[A/G]AACAAAATTTGGTAT | 237711 |
rs26843897 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml6 | GRCm38.p3 | 11:29904440 | AAGAGCAAAGAACTC[A/G]TAGTTACAGCTGGAT | 237711 |
rs26843898 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml6 | Mm_Celera | 11:29903858 | CTTGGTATTATTGGA[A/G]TTCAGTGGACTCTGC | 237711 |
rs26843899 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml6 | Mm_Celera | 11:29903784 | TATTTGTTCAGTTAC[C/T]GGGGATAGCATTTCT | 237711 |
rs26843900 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eml6 | GRCm38.p3 | 11:29901809 | CACTGAATACATTTC[A/G]GAGTTTTTACCTACT | 237711 |
rs26843901 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Eml6 | GRCm38.p3 | 11:29901761 | CAGTGATTCGGACTA[C/T]GGTAATACAGAGATA | 237711 |
rs26843902 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Eml6 | GRCm38.p3 | 11:29901755 | GAAATCCAGTGATTC[G/T]GACTATGGTAATACA | 237711 |
rs26843903 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml6 | Mm_Celera | 11:29898278 | GCCACATGTTAAGAG[A/G]TCTTGGCTCTCAGTA | 237711 |
rs26843904 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Eml6 | Mm_Celera | 11:29898237 | CTGATATAGGGGTTC[C/T]TGCAGGATGCCTCTT | 237711 |
rs26843905 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Eml6 | Mm_Celera | 11:29898232 | TAACACTGATATAGG[A/G]GTTCCTGCAGGATGC | 237711 |
rs26843906 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29897701 | CCCAGGAGGCGCAGA[C/T]GGAGGATTTACAACT | 237711 |
rs26843907 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Eml6 | Mm_Celera | 11:29897584 | GTCTGTAAAGTTTCT[C/G]ACAGGCCAGCAAAAC | 237711 |
rs26843908 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29897565 | CAGGATCCAAACATG[A/C]AAAGTCTGTAAAGTT | 237711 |
rs26843909 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29897536 | ATATCACACTCATTC[A/G]TTCTTTTTGACCACA | 237711 |
rs26843910 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Eml6 | Mm_Celera | 11:29897486 | CCCCACACTAGATGG[C/T]CTCCAGTAGGTCTCA | 237711 |
rs26843911 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:29897127 | TGACATACTCTACAG[A/T]TCCGCAAAGGTCTTA | 237711 |
rs26843912 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:29897096 | ATATGGCAAATTTAC[A/G]TTTAAAGACATAAAA | 237711 |
rs26843913 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml6 | Mm_Celera | 11:29897000 | AGCACTGAACATCTG[C/T]TTTGCTCCTGAATAA | 237711 |
rs26843914 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Eml6 | GRCm38.p3 | 11:29896776 | TTGCCAGGCATGCCT[G/T]CATGAGGTTACCATT | 237711 |
rs26843915 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Eml6 | Mm_Celera | 11:29896759 | CCACATAATCCCTGA[A/T]CTTGCCAGGCATGCC | 237711 |
rs26843916 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Eml6 | Mm_Celera | 11:29896644 | ACAACAAATACCAAA[A/G]AGGAAGGTAAGGAAC | 237711 |
rs26843917 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Eml6 | Mm_Celera | 11:29896607 | TGGTGTTTAACTGGG[A/G]CCTCATTAGACAAGG | 237711 |
rs26843918 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Eml6 | Mm_Celera | 11:29896591 | AGTAAGATGATGACG[A/T]TGGTGTTTAACTGGG | 237711 |
rs26843919 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Eml6 | Mm_Celera | 11:29896545 | TATCGTGTAATCACA[C/T]CATTAGAAACAATTT | 237711 |
rs26843920 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29895908 | CCTAAGCCCTTCACA[A/C]AGTACAGTAACTGCT | 237711 |
rs26843921 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29895870 | GCAGCTGCAGTGAAA[A/C]TGGAGACATCTAGAA | 237711 |
rs26843922 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29895849 | ACTCACCTCACCTCA[C/T]AGGATGCAGCTGCAG | 237711 |
rs26843923 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29895440 | GAAAACATCCTCTAA[A/C]GCTTGGTTTGTTTAC | 237711 |
rs26843924 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Eml6 | GRCm38.p3 | 11:29895128 | CAAATTCTCACTAAA[A/C]TAACAATCTGCCCTT | 237711 |
rs26843925 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29894280 | CAATTGTCAGGGCCA[A/G]AAAAAGAACCCAGCC | 237711 |
rs26843926 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Eml6 | Mm_Celera | 11:29893621 | GGCTAGTTATATATC[A/G]ATGTGGACAAATACC | 237711 |
rs26843927 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29885277 | CCAACAGTCTGACAG[A/C]GTTTTGCTGATAAAC | 237711 |
rs26843928 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Eml6 | Mm_Celera | 11:29885215 | CTTATAGAAGGTTCT[A/G]TATGTTGAGGCAATG | 237711 |
rs26843929 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eml6 | Mm_Celera | 11:29883532 | GGCAATCCTAATATT[C/T]TGTGCCTGCAGGAGA | 237711 |
rs26843930 | snp | A/G | 0.18 | 0.24 | intron-variant | Eml6 | Mm_Celera | 11:29882739 | ATTAGCATAACACAT[A/G]TCACCTAGCCATTTT | 237711 |
rs26843931 | snp | C/T | 0.42 | 0.183303 | intron-variant | Eml6 | GRCm38.p3 | 11:29881470 | AACCAAGACAAATGG[C/T]TTTCACCGTAGATGA | 237711 |
rs26843932 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Eml6 | GRCm38.p3 | 11:29881084 | TATATGACAACTGAG[C/T]CTTCTGAAACAAAGA | 237711 |
rs26843933 | snp | C/T | 0.18 | 0.24 | intron-variant | Eml6 | GRCm38.p3 | 11:29880149 | CATATTCTGGGAAAC[C/T]GTTCAGCTTTTTCAC | 237711 |
rs26843934 | snp | G/T | 0.42 | 0.183303 | intron-variant | Eml6 | Mm_Celera | 11:29879752 | CACAACTCCCTAAGA[G/T]AGAATCAGTGCAGTC | 237711 |
rs26843935 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Eml6 | Mm_Celera | 11:29877777 | TCAATCTAAGACAGA[A/G]GCATGTGCCAAGAGG | 237711 |
rs26843936 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Eml6 | Mm_Celera | 11:29872663 | GCTGTTATACCTCTC[A/G]TGAGATGAGTTAGGC | 237711 |
rs26843937 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29862700 | GATTCTAGACCCATG[A/G]AAAGTCATACAGGAC | 237711 |
rs26843938 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | GRCm38.p3 | 11:29848784 | TTTCATGAGCACTTA[C/T]CACAAGCATAATCAT | 237711 |
rs26843939 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:29848435 | GAAACTTGCTATGGC[A/T]TTGGTTCTTGCAATC | 237711 |
rs26843940 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29848393 | TGACTACATACTTTA[A/G]GCTCTCCTCACTCGG | 237711 |
rs26843941 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:29848161 | CAATACCCTGAATTA[A/G]ATGCTAAACTTTCCC | 237711 |
rs26843942 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Eml6 | Mm_Celera | 11:29841697 | CTAACTTACTCACAG[A/C]TACTAAGGACTACAA | 237711 |
rs26843943 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Eml6 | Mm_Celera | 11:29840763 | AATACCCTGAGAAGG[C/T]CTGATGGAGAGAAGA | 237711 |
rs26843944 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Eml6 | Mm_Celera | 11:29840711 | CATCAGATCAAACAG[A/G]CTGTCAAGAAACTAT | 237711 |
rs26843945 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Eml6 | Mm_Celera | 11:29839961 | ACCACTGCAGGCTGC[A/G]GAGGCAATAGAAGCT | 237711 |
rs26843946 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29839631 | TACATCAAGCCACAG[A/G]AGCAAATGAGTAGAA | 237711 |
rs26843947 | snp | A/C | 0.375 | 0.216506 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29837734 | AGTGCAAGTAGGTGG[A/C]TGTATAAAAGTTAAA | 237711 |
rs26843948 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29837622 | TAATACAGAATTGAA[A/T]GATTAGTCCTAGGAT | 237711 |
rs26843949 | snp | A/C/G | 0.459184 | 0.136902 | intron-variant | Eml6, LOC105243970 | GRCm38.p3 | 11:29837487 | AATTTTCAAAACAAG[A/C/G]CCAGGATCATTGCTT | 237711 |
rs26843950 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29837255 | ATGATGCATTTTATG[A/T]CCCATTTTGTACTGT | 237711 |
rs26843951 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29837201 | CTTCAAGCACTTTGA[A/G]CTGATGTCCATTCTG | 237711 |
rs26843952 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29837095 | TCTCAAATGCACATT[A/G]ATTTAAACAAGTTAT | 237711 |
rs26843953 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836933 | GACTCGAGTCCACTC[A/T]TAAGGTCTGGAGATA | 237711 |
rs26843954 | snp | A/C/T | 0.48 | 0.0979796 | synonymous-codon, intron-variant | Eml6, LOC105243970 | GRCm38.p3 | 11:29831168 | AACGTCAGAGAAGTC[A/C/T]GAGTCAGATTCCTCA | 237711 |
rs26843955 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29829638 | TATGTGGAAACACTG[A/G]AAAATAAGTCACAAA | 237711 |
rs26843956 | snp | A/T | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29827475 | TATGCCACTGCTGCC[A/T]GCTTTCTTACTCTGG | 237711 |
rs26843957 | snp | A/C | 0.396694 | 0.202437 | intron-variant, upstream-variant-2KB | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29827391 | CCTGGCTTGTTCTCA[A/C]AGCCTGCATGCTCAG | 237711 |
rs26843958 | snp | A/G/T | 0.297521 | 0.245442 | intron-variant, upstream-variant-2KB | Eml6, 4931440F15Rik, LOC105243970 | GRCm38.p3 | 11:29827303 | TTAAGAGATCGTCAC[A/G/T]CATACTGCCAGCAGT | 237711 |
rs26843959 | snp | C/T | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29826984 | TGTCCTTATGACCAA[C/T]TTCCCAGGTGACATA | 237711 |
rs26843960 | snp | A/G | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29826855 | CACACACTGGCATTC[A/G]ATGGATAAGGAGTTT | 237711 |
rs26843961 | snp | A/C | 0.459184 | 0.136902 | intron-variant, utr-variant-5-prime | Eml6, 4931440F15Rik, LOC105243970 | GRCm38.p3 | 11:29825521 | TCCTTCACCTTCTCC[A/C]GGGCTGTCATCTTAG | 237711 |
rs26843962 | snp | A/T | 0.473373 | 0.11227 | intron-variant, utr-variant-5-prime | Eml6, 4931440F15Rik, LOC105243970 | GRCm38.p3 | 11:29825506 | CGGTCGCCAGAGACA[A/T]CCTTCACCTTCTCCA | 237711 |
rs26843963 | snp | C/T | 0.132653 | 0.220748 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29825423 | CAGCTTGCCGTCGTG[C/T]GCCGCATTGTACACC | 237711 |
rs26843964 | snp | G/T | 0.459184 | 0.136902 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | GRCm38.p3 | 11:29825330 | GATTAGCAGTGGCGT[G/T]CCACCGCCGGCCACC | 237711 |
rs26843965 | snp | A/G | 0.46281 | 0.131194 | intron-variant, missense | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29825146 | CCGAGGCGCCTCGGT[A/G]CAGAAGGCTACGCAC | 237711 |
rs26843966 | snp | C/T | 0.244898 | 0.249948 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29825102 | GGCGGCGCGCAGCGG[C/T]GTGGAGTTGGTGCAC | 237711 |
rs26843967 | snp | C/T | 0.426035 | 0.177515 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | GRCm38.p3 | 11:29825000 | GGAGATCATAAGGCA[C/T]GTGTGGCCGTGGCGA | 237711 |
rs26843969 | snp | A/C | 0.142012 | 0.225474 | intron-variant, missense | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29824915 | CGGTGTTGCCCTTGG[A/C]GCTGCGCCGGTTCAC | 237711 |
rs26843970 | snp | C/T | 0.444444 | 0.157135 | intron-variant, missense | Eml6, 4931440F15Rik, LOC105243970 | GRCm38.p3 | 11:29824846 | TGCGCGCGTGGCAGC[C/T]CAGCAGCAGTTGTAG | 237711 |
rs26843971 | snp | A/G | 0.142012 | 0.225474 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29824577 | CCTTTTCTTATCCAC[A/G]TAGGTGGCACCCAGC | 237711 |
rs26843972 | snp | C/G | 0.444444 | 0.157135 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29824514 | GCCTCCACCCTGGTG[C/G]CGGAGTTCCATCGCC | 237711 |
rs26843973 | snp | C/T | 0.408163 | 0.193609 | intron-variant, missense | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29824396 | CCTGCATCCGCATCT[C/T]ATCAGGATCTGTAAT | 237711 |
rs26843974 | snp | C/T | 0.132653 | 0.220748 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | GRCm38.p3 | 11:29824361 | TGAGGGGCCCAAGAT[C/T]CTCTCCCGTATCAGC | 237711 |
rs26843975 | snp | A/G | 0.426035 | 0.177515 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29824358 | ATGTGAGGGGCCCAA[A/G]ATTCTCTCCCGTATC | 237711 |
rs26843977 | snp | C/T | 0.132653 | 0.220748 | intron-variant, missense | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29824168 | AGTGGTCCTGCAGCA[C/T]GTAGGAGAAGAGCTC | 237711 |
rs26843978 | snp | C/T | 0.408163 | 0.193609 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29823977 | CCTGGGGGTGCACTC[C/T]ACCTTCTCCAATAGG | 237711 |
rs26843979 | snp | C/G | 0.132653 | 0.220748 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29823875 | GGTCTCCTTGTCCAC[C/G]GCCATGTGTAGTGGG | 237711 |
rs26843980 | snp | C/T | 0.459184 | 0.136902 | intron-variant, missense | Eml6, 4931440F15Rik, LOC105243970 | GRCm38.p3 | 11:29823846 | ACGCCCACATGATAC[C/T]GGCCCACGTTGGTGG | 237711 |
rs26843981 | snp | A/G | 0.459184 | 0.136902 | intron-variant, synonymous-codon | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29823647 | CGAGTCCAGCAGCTC[A/G]TAGGCAGTCTTTTTG | 237711 |
rs26843982 | snp | A/G | 0.408163 | 0.193609 | intron-variant, utr-variant-3-prime | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29823232 | GTCAGTGCCCACTGC[A/G]GGAAGGAGACAGCTT | 237711 |
rs26843983 | snp | A/T | 0.142012 | 0.225474 | intron-variant, utr-variant-3-prime | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29823084 | CAAAGTACTGACAAC[A/T]CCCAACTCAGTCATT | 237711 |
rs26843984 | snp | C/G | 0.459184 | 0.136902 | intron-variant, utr-variant-3-prime | Eml6, 4931440F15Rik, LOC105243970 | GRCm38.p3 | 11:29823004 | CACAGAAATGAGGAG[C/G]CTTCCCAGGACCTTG | 237711 |
rs26843985 | snp | A/G | 0.408163 | 0.193609 | intron-variant, utr-variant-3-prime | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29822888 | GGTTGGGAACTGTCC[A/G]TCCATCCAGAGGGCG | 237711 |
rs26843986 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29821442 | GACACGGTGATGGAA[A/T]AGCCCTGAGTAGCAC | 237711 |
rs26843987 | snp | C/T | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | Mm_Celera | 11:29818796 | CAGAACCTTCATGTC[C/T]TATGCTTGTTCCTAC | 237711 |
rs26843988 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29815689 | TGTGCTTCCAGAAGA[C/T]TCCAGAAATGATCAG | 237711 |
rs26843989 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29815468 | GTAGCCGCTTATCTC[A/G]CGCCTCAAGACTTGA | 237711 |
rs26843990 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29815189 | TGATTTGCAATGTGA[A/G]GCAGAACAAAGCTCA | 237711 |
rs26843991 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29814703 | AAAGGTGGTTCAGCA[C/T]TTGAGTAGTCGGCTA | 237711 |
rs26843992 | snp | A/C | 0.32 | 0.24 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29813583 | TTGTGACTGTTCTAA[A/C]AGAAACAAAGGCATT | 237711 |
rs26843993 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Eml6, LOC105243970 | GRCm38.p3 | 11:29813508 | GAAACATAAAGTGGG[C/T]TGGTATGAGAACAAG | 237711 |
rs26843994 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29812172 | TCATTGCACTGTCAC[A/G]AAACAAAAATGGTTC | 237711 |
rs26843995 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Eml6, LOC105243970 | GRCm38.p3 | 11:29811906 | ATAGTTCTAAGGCAG[A/T]TAATGTCAACAGTAA | 237711 |
rs26843996 | snp | A/T | 0.32 | 0.24 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29811796 | ATAGTCCCTTGTGAG[A/T]TGGTTCTTTTCTCCT | 237711 |
rs26843997 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29811753 | TTCCCTGTAGAGACT[G/T]GACCTTACCTTTGAA | 237711 |
rs26843998 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29811304 | AGGAGAATGGGGATG[A/C]TAAAGATGTATCTAT | 237711 |
rs26843999 | snp | C/G | 0.32 | 0.24 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29809692 | GGAATGTACTGGAAG[C/G]GAGTAAATTTAGCTG | 237711 |
rs26844000 | snp | C/T | 0.32 | 0.24 | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29809602 | AGGTCAGCTACCCAC[C/T]GGACTTCCAACGGGA | 237711 |
rs26844001 | snp | A/C | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | Mm_Celera | 11:29808816 | AGATGGGCTATAAAC[A/C]GCAGTTGGTCTTGAG | 237711 |
rs26844002 | snp | A/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | Mm_Celera | 11:29808715 | CCTCTGACCGGGCCT[A/T]GCACTTGGCCGAGCT | 237711 |
rs26844003 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | Mm_Celera | 11:29808703 | CAGTGGTCCTGACCT[C/T]TGACCGGGCCTTGCA | 237711 |
rs26844004 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | Mm_Celera | 11:29808673 | CAACAAGCTAACTTC[C/T]CGGACTGTGGCTATC | 237711 |
rs26844005 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | Mm_Celera | 11:29808631 | GTAGGTCATAGCTCA[C/G]AGAGAGGGTATGAAA | 237711 |
rs26844006 | snp | A/G | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | Mm_Celera | 11:29808607 | CAACACAGACAGGAT[A/G]TTGGCAATGTAGGTC | 237711 |
rs26844007 | snp | C/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | Mm_Celera | 11:29808528 | GATCCCATGTAACAC[C/T]GTAGTAGACAGTATT | 237711 |
rs26844008 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | GRCm38.p3 | 11:29808448 | CAAGACTCCAGCCAC[A/G]ACTCTGTTCCATCTC | 237711 |
rs26844009 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Eml6 | GRCm38.p3 | 11:29806311 | TGCTCATCAATGCAA[C/T]AGTTACATTTACTTC | 237711 |
rs26844010 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29806124 | TTGGATGTAATTCTG[A/G]GATAGTGAGACCTTG | 237711 |
rs26844011 | snp | C/G | 0.391111 | 0.206368 | missense | Eml6 | Mm_Celera | 11:29805772 | CAACTTGTCAGCATG[C/G]TGTGGATTACACTTT | 237711 |
rs26844012 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Eml6 | Mm_Celera | 11:29805591 | ACTTATCCATTAAAT[A/C]GTCCAATGCAAAGCT | 237711 |
rs26844013 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29803720 | GTTCTAAATCTCTGG[A/C]TTCTGCGATCCCAGA | 237711 |
rs26844014 | snp | A/G | 0.32 | 0.24 | intron-variant | Eml6 | Mm_Celera | 11:29802926 | GAAATCATCCTTGAT[A/G]TACCTGCCAGAGACA | 237711 |
rs26844015 | snp | C/G | 0.32 | 0.24 | intron-variant | Eml6 | Mm_Celera | 11:29802319 | GTGAACACCACACTG[C/G]AGCATCCCAGGAAGT | 237711 |
rs26844016 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29799636 | TTCTGCCAGATGTCA[G/T]ACTCCAACTCCAGGT | 237711 |
rs26844017 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Eml6 | Mm_Celera | 11:29799094 | GTCTCAGGCCATCTA[C/T]ACCTGGTACACAGAT | 237711 |
rs26844018 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Eml6 | Mm_Celera | 11:29798765 | CCAGGGAAGGGCATA[C/T]GTGCTTTACCAGATG | 237711 |
rs26844019 | snp | G/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29798552 | CACAGGAACGTCTTC[G/T]CAAACCTGTTATTAA | 237711 |
rs26844020 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29795109 | ATATTTTTGGGATTG[A/T]AACAGGTACTCTCAT | 237711 |
rs26844021 | snp | C/T | 0.497778 | 0.0332592 | missense | Eml6 | GRCm38.p3 | 11:29784228 | TCCAGGTGTCCCATT[C/T]TATCTTCTCAGCCTG | 237711 |
rs26844022 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:29784043 | GAACAGATGAAATCT[A/T]TAACAAACATACAAT | 237711 |
rs26844023 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Eml6 | GRCm38.p3 | 11:29783989 | GTATTTAAATAAAAA[A/G]AACCATTCGGGTACA | 237711 |
rs26844024 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29783875 | ATCTGGGGACCACTA[C/T]ATCATGAGAACTTCA | 237711 |
rs26844025 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29782531 | TGGGGGCTGCCAGCT[C/T]ATCAACAGGGAGATG | 237711 |
rs26844026 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Eml6 | Mm_Celera | 11:29782428 | GGAAAGAAAGATGGT[A/G]CAAAGCAGGGTGGAG | 237711 |
rs26844027 | snp | A/C/T | 0.429688 | 0.173817 | intron-variant | Eml6 | GRCm38.p3 | 11:29782097 | CTACATGTATGGCTC[A/C/T]GCTATGGTTTCAACT | 237711 |
rs26844028 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29781941 | AGTGGGATAAGCATT[C/T]CAAAGGCTTTGAAAG | 237711 |
rs26844029 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Eml6 | GRCm38.p3 | 11:29781231 | CATGTACTGTCAAAC[A/G]TGATCACAAAGGATG | 237711 |
rs26844030 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Eml6 | GRCm38.p3 | 11:29780956 | GCACAAGCACTAAAA[A/C]AGGGTCTTGACAATG | 237711 |
rs26844031 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Eml6 | GRCm38.p3 | 11:29780930 | GGTAGGGGAAATGAT[G/T]TCTATACTGGGCACA | 237711 |
rs26844032 | snp | G/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29779780 | TAAACCATGCAAAGT[G/T]TCAAAGTTGTGACAA | 237711 |
rs26844033 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29778962 | CACAGTCACAGTACA[A/G]TCAGGGATACAGTGT | 237711 |
rs26844034 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29778897 | ACTAACTGTGTCACA[C/T]AGTGCTCCATGCTCA | 237711 |
rs26844035 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Eml6 | Mm_Celera | 11:29778865 | ACATCTGATTCTGGC[A/G]GCTCCTTTTATAGCT | 237711 |
rs26844036 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Eml6 | GRCm38.p3 | 11:29778697 | TGAACAGACATTTTT[C/T]AAAGAAGTTTGTAGA | 237711 |
rs26844037 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Eml6 | Mm_Celera | 11:29778435 | AACTACCTATTCCTC[A/C]CAAAAGCACCAAGAG | 237711 |
rs26844038 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eml6 | Mm_Celera | 11:29777706 | GTCTCTCTGACATCA[A/G]AAGAGTCAGGCCCGT | 237711 |
rs26844039 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Eml6 | GRCm38.p3 | 11:29777570 | TTGCTTGTATCATGA[C/G]AATACATGCTCCATG | 237711 |
rs26844040 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Eml6 | Mm_Celera | 11:29776073 | TCTGCCTCATGCATC[A/G]TGCCAACAACACACC | 237711 |
rs26844041 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Eml6 | Mm_Celera | 11:29772609 | CAGAAGCAGAGAGTG[A/G]GAGTCCTCGATCCTT | 237711 |
rs26844042 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29770494 | CAAAAGAGCTAACCT[A/G]AAGCTAAGCCCTATC | 237711 |
rs26844043 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29770202 | AAGAAATAGGGCATG[C/T]TCCATAAACACATCA | 237711 |
rs26844044 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29770149 | GCCCTTGCTGCTGAC[C/T]CTCAAGTCTGTGTGT | 237711 |
rs26844045 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29768775 | CCTCTGTGAAGGCCA[C/T]GGAGCTCAGGAGGCT | 237711 |
rs26844046 | snp | C/G | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29768520 | CAGTATTCCATACTA[C/G]CAAGCTCTTGAATGT | 237711 |
rs26844047 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29768030 | GTAGCTAGGCTTCTC[C/T]CGCACTTTACCTCTG | 237711 |
rs26844048 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29767171 | CTGTGCAAGCTGAAT[A/G]GAAAGTAAGGTTCTG | 237711 |
rs26844049 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29766926 | GTGCCGATTCTTCTT[C/T]CCATTGGCCTGGCTG | 237711 |
rs26844050 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29766890 | TTATGTCGGCATAAG[A/G]AGGATGGGAGGCTCA | 237711 |
rs26844051 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Eml6 | GRCm38.p3 | 11:29766483 | CTACTGGAAATGCCA[C/T]GCTGAGAAACTCTGC | 237711 |
rs26844052 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29766396 | TGGGAGGAGCTGCCA[A/G]AAACTTAAAGCACAG | 237711 |
rs26844053 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29766267 | CTTCTTCCAGAGTGC[A/T]GTGGATACTTACTTG | 237711 |
rs26844054 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Eml6 | Mm_Celera | 11:29765164 | AAGTCATACCCTGGC[A/G]TCTTTGGGCAGACTG | 237711 |
rs26844055 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29765141 | GTGCACCAGGCTACA[C/T]GGTTACCAAGTCATA | 237711 |
rs26844056 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:29764551 | TGTAGCAGGACTTAG[A/G]AAGCAAGCTGTGGAA | 237711 |
rs26844057 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Eml6 | GRCm38.p3 | 11:29764019 | CATCGGGAATCAGAC[A/G]AACATGCATGATGGC | 237711 |
rs26844058 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Eml6 | Mm_Celera | 11:29762942 | ACTTGGCTCATGATG[A/G]CTCTTGTACTGTTCG | 237711 |
rs26844059 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29761932 | CCTAAATAAACTAAC[A/T]CGACTTTTACGTTCT | 237711 |
rs26844060 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29761835 | GGGAGGCCGATACCA[C/T]TCAATGAAGATACTG | 237711 |
rs26844061 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Eml6 | Mm_Celera | 11:29761315 | CTATTTCTGTGAATA[C/T]TGCTCCAGAGTCAAA | 237711 |
rs26844062 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29761195 | TCTGGTGGTGAGGAT[A/G]TGGATGTGAGTCTGT | 237711 |
rs26844063 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Eml6 | GRCm38.p3 | 11:29761131 | AATTACTGGACTCAG[C/G]GAGGAACATGAGCTA | 237711 |
rs26844064 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:29761100 | GACTCAGTGACTACA[C/T]TCAAATCTAGCCATG | 237711 |
rs26844065 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Eml6 | Mm_Celera | 11:29761075 | ACCCAAAAGGGAGGA[A/G]AATCAAAATGACTCA | 237711 |
rs26844066 | snp | C/G | 0.42 | 0.183303 | intron-variant | Eml6 | GRCm38.p3 | 11:29759925 | TCAACTGAGACATCA[C/G]CAAGAAAGGGCCTAA | 237711 |
rs26844067 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Eml6 | Mm_Celera | 11:29759270 | AGGCCGAGCATATGG[A/G]TATTTATGTCTGACA | 237711 |
rs26844068 | snp | A/C | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29759227 | GTCTGACTTGGCCAA[A/C]GAAAGACACTGAGGA | 237711 |
rs26844069 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Eml6 | Mm_Celera | 11:29759161 | GTGTCTGTGTTCCAT[C/T]AGAGGCCTTTCCTCA | 237711 |
rs26844070 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29757868 | TTGTGGGTCAGGCTG[A/G]CTCCCAGTGCAGTGT | 237711 |
rs26844071 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29755281 | AAAGTCACGACTAGA[A/G]TAGGAAATGACTGTG | 237711 |
rs26844072 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29755183 | CTTTAACTGTATCAG[A/C]TTCCTCTCAGACATC | 237711 |
rs26844073 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29755140 | GCCAAGGCTGGTCTT[A/C]CATTCACTCCGAATA | 237711 |
rs26844074 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Eml6 | Mm_Celera | 11:29753804 | AGGAAGTGGACACAT[C/T]AGACTTGAAACACCA | 237711 |
rs26844075 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Eml6 | Mm_Celera | 11:29753690 | GTTTGGACATTTTTG[C/T]ATCCCTATTGTGCGA | 237711 |
rs26844076 | snp | C/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29753234 | GTTCTGCAAACAAAG[C/G]ACACCTTGAGAACCG | 237711 |
rs26844077 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon | Eml6 | GRCm38.p3 | 11:29753123 | GGTGTACATTGTAAA[A/G]ACAGGACCTGTGTGA | 237711 |
rs26844078 | snp | A/G | 0.473373 | 0.11227 | synonymous-codon | Eml6 | GRCm38.p3 | 11:29753090 | TCCGCCAGTCACAAT[A/G]AGCCCATCTCGGAGG | 237711 |
rs26844079 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Eml6 | Mm_Celera | 11:29752949 | TCGGACTGTCCTGCA[C/G]AGCTGACAGACTGAT | 237711 |
rs26844080 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Eml6 | Mm_Celera | 11:29752926 | TTTGCTACCCTCTTA[A/G]AAAGACCTCGGACTG | 237711 |
rs26844081 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eml6 | GRCm38.p3 | 11:29752874 | ACAACAGCTTTTTGA[A/G]AAGTATAGCCTAAGG | 237711 |
rs26844082 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29752156 | GACAGTGGCTAAATG[A/G]CTTCCTGTCAGGGAG | 237711 |
rs26844083 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Eml6 | Mm_Celera | 11:29752134 | TTATGAGAACAGCGA[A/T]TGAAGTGACAGTGGC | 237711 |
rs26844084 | snp | C/G | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29751706 | AGGATATGCTGAGGC[C/G]TCTTGCGAAGGGCTG | 237711 |
rs26844085 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Eml6 | Mm_Celera | 11:29750784 | TCAAACATTTGTATC[C/T]CTCTCGTTCTCCTCC | 237711 |
rs26844086 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29750763 | CTGACGGGAAATCTG[A/T]CACTCTCAAACATTT | 237711 |
rs26844087 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Eml6 | Mm_Celera | 11:29750745 | TCCCAACCTTCCCGG[A/G]ATCTGACGGGAAATC | 237711 |
rs26844088 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29750243 | TGTGGACAGTAGTAA[C/T]AAATGTGGCTTCACC | 237711 |
rs26844089 | snp | A/T | 0.495868 | 0.0452663 | intron-variant | Eml6 | Mm_Celera | 11:29749595 | AATGGTGTTATGCAG[A/T]CTTTGGTAGAATTAC | 237711 |
rs26844090 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Eml6 | Mm_Celera | 11:29749029 | AGGGTAAAGGTGACT[A/G]GGGATATGTTCCCTG | 237711 |
rs26844091 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Eml6 | Mm_Celera | 11:29748706 | TCCAGCCCATTCTGG[A/T]ATGCAGCAGCCATAC | 237711 |
rs26844092 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Eml6 | Mm_Celera | 11:29748653 | GTAGGACCCCTTGAT[C/T]TTGCCTCTCAGCTGT | 237711 |
rs26844093 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Eml6 | GRCm38.p3 | 11:29748562 | CCCACCACCGCCTGG[C/T]TTAAGCACTCCTCTT | 237711 |
rs26844094 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Eml6 | GRCm38.p3 | 11:29747638 | ACGCTTTTCTTTAAA[C/T]CCAAACTCAGCTCCT | 237711 |
rs26844095 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Eml6 | Mm_Celera | 11:29747624 | ACTCTGCCCCAGTTA[C/T]GCTTTTCTTTAAATC | 237711 |
rs26844096 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Eml6 | Mm_Celera | 11:29747424 | ACCAGAGTTCTCTTC[A/C]TTTACCTTGTCCAGG | 237711 |
rs26844097 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Eml6 | GRCm38.p3 | 11:29747247 | GGCTTGGGGTTGGTA[C/T]GAATGATTAAACAAA | 237711 |
rs26844098 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Eml6 | Mm_Celera | 11:29747016 | TAGGTCATTTGGTCA[C/T]GTGGGCACACCCTGC | 237711 |
rs26844099 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Eml6 | Mm_Celera | 11:29747007 | TAGGAATTGTAGGTC[A/G]TTTGGTCACGTGGGC | 237711 |
rs26844100 | snp | A/G | 0.495868 | 0.0452663 | synonymous-codon | Eml6 | GRCm38.p3 | 11:29746872 | ATCAGCCTTGTCTGC[A/G]TTTCGTGGCCAGATT | 237711 |
rs26844101 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Eml6 | Mm_Celera | 11:29746540 | CTTCTCTCCCCTGAT[A/G]CCCAGGCTCAAGTCT | 237711 |
rs26844102 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Eml6 | Mm_Celera | 11:29746213 | CCCAACTAGCAGAAC[C/T]GCCCGAGGAGCCAAC | 237711 |
rs26844103 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Eml6 | Mm_Celera | 11:29745901 | CTCAAGGACAAATGG[A/G]TGAAGGTTGATTTAA | 237711 |
rs26844104 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Eml6 | Mm_Celera | 11:29745768 | GACTCAGCATCTCCC[A/G]TTTCTCATGGCAACT | 237711 |
rs26844105 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Eml6 | Mm_Celera | 11:29745433 | CAGGCTTGCTAGACC[C/T]GTTTTACTTTTTCAG | 237711 |
rs26844106 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29745261 | GCAGGCAGGCCATCA[C/T]GGCGCACTGTGTTCT | 237711 |
rs26844107 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Eml6 | Mm_Celera | 11:29745258 | TCAGCAGGCAGGCCA[G/T]CACGGCGCACTGTGT | 237711 |
rs26844108 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29745100 | TGGGCTGGCCAGTTC[A/G]TTTAGGCCTTTTCTT | 237711 |
rs26844109 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:29744933 | ACTTGGCAGCCCAAC[C/T]TCACACTATCTGTCC | 237711 |
rs26844110 | snp | A/T | 0.5 | 0 | downstream-variant-500B, intron-variant | Rtn4, Eml6 | Mm_Celera | 11:29744867 | TGATGTGTGTCTCCC[A/T]TAGACTCCTTTTGCT | 237711 |
rs26844111 | snp | C/T | 0.152778 | 0.230321 | downstream-variant-500B, intron-variant | Rtn4, Eml6 | Mm_Celera | 11:29744667 | TGCTGCCAAGTGTTC[C/T]AGACTGAAAAGTGTA | 237711 |
rs26844112 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B, intron-variant | Rtn4, Eml6 | Mm_Celera | 11:29744664 | TAATGCTGCCAAGTG[C/T]TCCAGACTGAAAAGT | 237711 |
rs26844113 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Rtn4, Eml6 | Mm_Celera | 11:29744032 | AAGGAAGAAGACGAC[A/G]TGGGAGGTGAGGCAG | 237711 |
rs26844114 | snp | C/T | 0.396694 | 0.202437 | utr-variant-3-prime | Rtn4, Eml6 | Mm_Celera | 11:29743946 | TTATAACTGCTTTCC[C/T]AGAGCAGGACATAGT | 237711 |
rs26844115 | snp | A/C | 0.459184 | 0.136902 | utr-variant-3-prime | Rtn4, Eml6 | Mm_Celera | 11:29743850 | ACTAAACAGCAAGAC[A/C]GCTCACTCGTCACAC | 237711 |
rs28308206 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Eml6 | Mm_Celera | 11:29943835 | ATTGGCTGCCTCTGA[C/T]AATCTGTCTGTTCTA | 237711 |
rs29383727 | snp | A/C | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29804408 | GAAGCTGAATGGCAT[A/C]GATGAATTAGTACTA | 237711 |
rs29384092 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29804099 | AATCCTCAAACTAAA[C/T]ATAAGTAGAGTATAT | 237711 |
rs29385231 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29772119 | CAGAGCCAGTGAGAG[A/G]CTCAGCAGGTAAACT | 237711 |
rs29386138 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29795424 | GCTGAGAGCACCTCA[A/G]GCTGAAAGTGCCTCA | 237711 |
rs29388307 | snp | A/C | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29804724 | CTAGGTTTACATGTG[A/C]TGTGTCACTGGAAAG | 237711 |
rs29388356 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29761832 | AATGGGAGGCCGATA[C/T]CACTCAATGAAGATA | 237711 |
rs29388683 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29786486 | CTATCCTCAAACAAC[G/T]GAGTGACTGGCCTTT | 237711 |
rs29394270 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29757978 | AAAATGTAAACATCC[A/G]TTTAAAGCCCTTCTT | 237711 |
rs29394353 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29792502 | ATGCATGTGTATGCA[C/G]TCACATGCTTACATG | 237711 |
rs29394514 | snp | C/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29789679 | CTGCCAACAGTCCTA[C/G]CGACCATGAAATCCA | 237711 |
rs29396728 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29795117 | GGGATTGTAACAGGT[A/G]CTCTCATTAAACAGT | 237711 |
rs29397074 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eml6 | GRCm38.p3 | 11:29785132 | TTATCATTATGGAAA[A/G]TATTGCTTATTATTA | 237711 |
rs29397287 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29804956 | ACTTCCTAACTGAGC[A/T]AGGACTGTTTTTAGA | 237711 |
rs29399574 | snp | C/G | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29798546 | GGCTGACACAGGAAC[C/G]TCTTCTCAAACCTGT | 237711 |
rs29400285 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29797106 | AGCAGGTTGGCTCAG[A/C]CCTGTTCTGCCTCTG | 237711 |
rs29401448 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29791610 | CTATCTCTGCCAAGA[A/G]CTGAAAATTGCTTGA | 237711 |
rs29401975 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29802898 | GGGTCTGAATCCCAA[C/T]ACTGGATACTAGGAA | 237711 |
rs29402170 | snp | A/C | 0.444444 | 0.157135 | synonymous-codon | Eml6 | Mm_Celera | 11:29749388 | TGTCTGCTCAGAAGA[A/C]CCCACAGCTAAGAAT | 237711 |
rs29403097 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29752810 | TCCCTCCTTTTTGTC[C/T]TCCCTTTCCCCAAGA | 237711 |
rs29405164 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29771825 | CTTTAAATGTATATT[C/T]ATTCTTCCAGTTCTG | 237711 |
rs29407146 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29796550 | GATGGAAGGAGGTTT[C/T]CTATGTCCAGGCTTC | 237711 |
rs29407238 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29747725 | TAGGGTGTGTTCTAC[C/T]TCCCCAACCCCTGTC | 237711 |
rs29407608 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Eml6 | GRCm38.p3 | 11:29748812 | TTCTAAAACTTATTG[A/T]AATTAGTCCTCCGGT | 237711 |
rs29407620 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29802912 | ATACTGGATACTAGG[A/C]AATCATCCTTGATAT | 237711 |
rs29407821 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29796702 | TCCTTGGCTTCTTCA[G/T]CTTACCCTATTTCCT | 237711 |
rs29408774 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Eml6 | GRCm38.p3 | 11:29746800 | GAGCTTCAGCAGCCC[A/G]AAGTCATCCCCTGTG | 237711 |
rs29410217 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29784735 | TGCCAATATTGTCCT[C/T]CTCCATGGACAATGA | 237711 |
rs29411046 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29774115 | GCTGCCTGAAGGAAT[A/C]CAAGTGAAAGAGCCA | 237711 |
rs29411354 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29789050 | GCCAGCTGGCTCTGG[C/T]AAATGCTTTCACTAT | 237711 |
rs29413582 | snp | G/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29771849 | AGTTCTGTTCCTCTA[G/T]AGGATACTAATGAAG | 237711 |
rs29414207 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29772181 | AGACCCACATGACAG[A/G]AGGCAAGAATTGGTT | 237711 |
rs29419323 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29765882 | TCCAGAGTACACACA[A/G]GTTATATAATATACA | 237711 |
rs29420377 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | GRCm38.p3 | 11:29797187 | TCTGACACCTCTGTG[C/T]TTTTCTCCAAGATGC | 237711 |
rs29422178 | snp | A/C | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29771919 | TATAAAAATGCTTTT[A/C]TATTATAATGTAGTA | 237711 |
rs29422550 | snp | C/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29795378 | CTGTGGAAGAGGAAA[C/G]AAGGCAAAGTAAACC | 237711 |
rs29423793 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29804648 | AGCAAACAGGTTATG[A/G]AAATAACCTCTGGTC | 237711 |
rs29425412 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29784698 | CCATGTTTAACAGCA[C/T]GCCTGACCTTCACCC | 237711 |
rs29425413 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml6 | GRCm38.p3 | 11:29785064 | AGACGTGGGAAAAAG[A/G]AAATAGTTTGACATT | 237711 |
rs29425836 | snp | C/T | 0.48 | 0.0979796 | utr-variant-3-prime | Rtn4, Eml6 | Mm_Celera | 11:29743616 | TTTTAGTGCACAGAC[C/T]GGAAGGACTCGGTGG | 237711 |
rs29426822 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | GRCm38.p3 | 11:29797191 | ACACCTCTGTGCTTT[C/T]CTCCAAGATGCTGCT | 237711 |
rs29427070 | snp | G/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29756009 | GATTGCTCTCCAGGA[G/T]AGCAGAGGTTGTGTT | 237711 |
rs29428369 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29772828 | CCAACTGAATACAGT[A/C]AATAAAAATCTCTAT | 237711 |
rs29429445 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29798977 | TCTCAATATCTCAAG[C/T]CTTCTTTTCCGACCA | 237711 |
rs29429452 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29757643 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 237711 |
rs29429914 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29756679 | AGTGACTTAGTCTCT[C/T]GTCTGTTCAGAAGAA | 237711 |
rs29431813 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | GRCm38.p3 | 11:29752817 | TTTTTGTCCTCCCTT[C/T]CCCCAAGAGCTGCTA | 237711 |
rs29432248 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29804289 | CTAAAAGAGCAGCTC[A/T]ACCATAAAAAACTGT | 237711 |
rs29432494 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml6 | GRCm38.p3 | 11:29798892 | TATAGAGTCTACCTC[C/T]GTCCAGGGTTCTTTC | 237711 |
rs29432851 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29774792 | CTCCTTCTTTCCCCC[C/T]CTTTCCCAGGAGGCT | 237711 |
rs29432880 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29750509 | TCAGTGAGTAGAAGC[C/T]GTTTTTAGTAAACTT | 237711 |
rs29435368 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29790742 | CCCAGTCTGAGACTA[C/T]CTCAAAAAATACTTA | 237711 |
rs29436053 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29798691 | GGGGTCCTAGGTCAC[C/T]AACCAGGACCCTCCT | 237711 |
rs29436116 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29756156 | ACACAGCAACTGAAA[C/G]TCATCACAGTAGTAA | 237711 |
rs29437183 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29772465 | CTGTGCCTTAGGTCA[A/G]GCAAGATTTTGATTT | 237711 |
rs29437344 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29750439 | TAGTAGCGTTGGAAG[A/C]TTTTTGTAAGTATTA | 237711 |
rs29438211 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29757645 | GAACTCAGAAATCTG[C/T]CTGCCTCTGCCTCTC | 237711 |
rs29442671 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29795624 | ACAAATATCCAGGTA[C/T]ATGGTAAACTTTCCA | 237711 |
rs29443023 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29776782 | GCTTCCTCCCCTAGT[C/G]AGGGAAGCCTAGTCC | 237711 |
rs29445628 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29762591 | AACTTGTTTTCTAAT[A/G]TTCCTTTCACCTGAA | 237711 |
rs29446565 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29784780 | GGGAAAATTGCTTTC[A/G]GGTAGGAATTATTGA | 237711 |
rs29447163 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29802285 | TGGTCTGTGGCCATT[C/T]GCTGCACACCAACAG | 237711 |
rs29449841 | snp | G/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29789600 | CCTTTTCAAGTGATG[G/T]CTCCATTTTGAGGTA | 237711 |
rs29449948 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | GRCm38.p3 | 11:29796585 | TACCTTCACTCCAAA[C/T]TTTCTCTCTGTGCTT | 237711 |
rs29450621 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29803727 | ATCTCTGGATTCTGC[A/G]ATCCCAGACAGACTA | 237711 |
rs29450702 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29804523 | CTTTGTAGAGAATAC[A/G]GTAAGGCAGATGAGT | 237711 |
rs29450723 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29773363 | TGGATGGAGCTTGGG[A/G]ATTCTTGTGGAAGAA | 237711 |
rs29451469 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29796930 | CTTCCTCCTTTTGGA[C/T]ACTGGGGTCACTTAC | 237711 |
rs29452150 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29757629 | AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCTG | 237711 |
rs29452814 | snp | G/T | 0.48 | 0.0979796 | utr-variant-3-prime | Rtn4, Eml6 | Mm_Celera | 11:29743575 | AAAATGGCAACTTCA[G/T]ATAACTAGAAACTCA | 237711 |
rs29456572 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29773551 | GCAGATGGTTTTCAC[A/G]TGGGTCCAAGACAAT | 237711 |
rs29456836 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29786658 | GTTTAATTATGGAAA[A/C]ATTTCAATCAGGCTT | 237711 |
rs29457272 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29766363 | AGCATCTATAAACAG[C/T]GTTTGAAATATCAGA | 237711 |
rs29457463 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29771969 | ACAATTAAATTTTTT[A/T]AAAAAAACTTCTTAG | 237711 |
rs29457740 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29796469 | ATGACTTTAAATGGC[C/T]GCCTAATGTCACTTT | 237711 |
rs29457779 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29747213 | TGGGCTTGGCAAAAC[A/G]TTTGAACTTGCTGAA | 237711 |
rs29458758 | snp | C/G | 0.444444 | 0.157135 | missense | Eml6 | Mm_Celera | 11:29746793 | AATCAAAGAGCTTCA[C/G]CAGCCCGAAGTCATC | 237711 |
rs29459536 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Rtn4, Eml6 | Mm_Celera | 11:29743550 | AAAATGCTTATTTCA[A/G]CCTTTCTCTAAAATG | 237711 |
rs29459650 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29804847 | CCAGGAAGTCCAGGG[A/T]TGAGAAAATGGAGAA | 237711 |
rs29460022 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29778606 | CACTCATATACATAC[A/G]TACACACACACACTT | 237711 |
rs29460532 | snp | A/C/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29749788 | CTATATACCTGATAT[A/C/T]TTTTATTTTTTTGTA | 237711 |
rs29461283 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29775317 | TTTCTTCACTGTATT[C/T]AAGGATGAATTATTT | 237711 |
rs29462320 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml6 | GRCm38.p3 | 11:29798900 | CTACCTCCGTCCAGG[A/G]TTCTTTCACTTCAGG | 237711 |
rs29462888 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29802314 | AGGTAGTGAACACCA[C/T]ACTGGAGCATCCCAG | 237711 |
rs29463401 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29774102 | ATACAAGGTTGGGGC[C/T]GCCTGAAGGAATCCA | 237711 |
rs29463865 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29758562 | CTTTTGGTGACTATT[A/G]GTCACTTCAGTTCTA | 237711 |
rs29464121 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29773696 | GTGGGGCATTTGAAT[A/T]TGGGAAGTGGTGGGG | 237711 |
rs29464785 | snp | A/T | 0.48 | 0.0979796 | utr-variant-3-prime | Rtn4, Eml6 | Mm_Celera | 11:29743563 | CAACCTTTCTCTAAA[A/T]TGGCAACTTCATATA | 237711 |
rs29464942 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29916235 | GAGGAACCCTGAGTT[C/T]TAAGAGGTAAAAAGG | 237711 |
rs29466369 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29766165 | GAAACCTGCATCAGG[C/T]AGTCTGCCCTTTTCA | 237711 |
rs29467582 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29802602 | CACCGCCAAGGCAGG[C/T]TAGCATAGTATCTTC | 237711 |
rs29467949 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29790076 | ACAAGAAGGAAGTGA[A/G]TTTTGGAGGTGAGTA | 237711 |
rs29469570 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29771339 | GAGGAGCTACCTAGT[C/T]CCCAAAAATCCCTAT | 237711 |
rs29469823 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29757958 | GATGGCATTTTTTTT[C/T]CCTCAAAATGTAAAC | 237711 |
rs29469906 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29798985 | TCTCAAGTCTTCTTT[C/T]CCGACCAAATGCTGT | 237711 |
rs29470317 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29756054 | AATGAAGTTGGCCCA[C/T]CCTTTAGCTTCAGAT | 237711 |
rs29470484 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | Rtn4, Eml6 | Mm_Celera | 11:29742695 | CACCTGTTTTCAAGA[A/G]AACATAGAACTCCAA | 237711 |
rs29473206 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29802052 | ATGTGTGCCAATGAA[C/T]GCTAAAGGTAGTCTG | 237711 |
rs29474879 | snp | C/T | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29802650 | GTGACAGGTATTCTC[C/T]ACAGATGAAATAAGC | 237711 |
rs29478428 | snp | C/G | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29782858 | TGACACATATACATA[C/G]TGACACACTGCAGTT | 237711 |
rs29478843 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29761170 | GGAAGATAGAGGCTG[A/T]TATATCTGATCTGGT | 237711 |
rs29479105 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29747096 | CAGAAAGAAAACTTT[G/T]ATTTTATTTTTTCTT | 237711 |
rs29481084 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29802053 | TGTGTGCCAATGAAC[A/G]CTAAAGGTAGTCTGG | 237711 |
rs29481516 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29801935 | GACAGAAAGTTCCAG[A/G]GAACATGTGACTTAA | 237711 |
rs29481768 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29791790 | GAGATGCTTATGGAA[C/T]AGAAAAATTCTCAAA | 237711 |
rs29482510 | snp | A/C | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29802668 | AGATGAAATAAGCCA[A/C]CTCAAGCCAGGTTTA | 237711 |
rs29483406 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29749073 | GTTTTTGTTTCTTAC[A/G]AAAAGACTTGTACAC | 237711 |
rs29483838 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29771752 | TGTCTTTTCAGTGTG[C/T]GACATTCATTGTTGG | 237711 |
rs29484207 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Rtn4, Eml6 | Mm_Celera | 11:29743826 | CCAGTCCTACCCAAG[A/G]GGGTGTAAACTAAAC | 237711 |
rs29484659 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29795827 | GCCCCCAGCTTTGGA[A/G]TTAGAGATGTATGCC | 237711 |
rs29485722 | snp | A/T | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29804617 | CACTCCTGGTAACTG[A/T]ACCTGACTATTCAGG | 237711 |
rs29485996 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29772452 | TGAGCAAAGGAAACT[A/G]TGCCTTAGGTCAGGC | 237711 |
rs29486982 | snp | C/T | 0.5 | 0 | intron-variant | Eml6 | GRCm38.p3 | 11:29798979 | TCAATATCTCAAGTC[C/T]TCTTTTCCGACCAAA | 237711 |
rs32029115 | snp | A/G | 0.375 | 0.216506 | intron-variant | Eml6 | Mm_Celera | 11:29855888 | CTATCATCATAGATG[A/G]ACAAACCAAGATATT | 237711 |
rs32954455 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eml6 | Mm_Celera | 11:29766344 | TATTAAAAGCCTCTT[C/T]CCAAGCATCTATAAA | 237711 |
rs32965649 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Eml6 | Mm_Celera | 11:29802338 | ATCCCAGGAAGTTCT[G/T]TGTAATCTTTACACC | 237711 |
rs33848872 | snp | A/G | 0.5 | 0 | intron-variant | Eml6 | Mm_Celera | 11:29797365 | CTTAAGTAAACTTTG[A/G]GCCTTGATCAGTATC | 237711 |
rs45642015 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29758690 | GGGACAGTGTTAGCC[C/T]TCTCCCAACATACCC | 237711 |
rs45642139 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29792875 | GGTTCCCAGCACCCA[C/T]GTCAGTAATCGGCTC | 237711 |
rs45679069 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29767950 | GAAATCTTGACTTCA[A/G]ATGGGCATGGGAGCT | 237711 |
rs45720166 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29768183 | CATTTACAGAAACAT[C/T]ATTAAATTCAATTAA | 237711 |
rs45745611 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29746104 | ATATGGTAGGAAATT[C/T]TTGGTTTTCCCCTAA | 237711 |
rs45765098 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29755359 | ATCTTCCTCATCCCA[A/G]ATCTATTCACCCCAG | 237711 |
rs45769682 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29768549 | GTTCCCTCTTCACCA[A/G]TGGAATGGGAATGCT | 237711 |
rs45791180 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29760241 | AGCCAAATTATTGTT[C/T]TCAGAATTATCATTT | 237711 |
rs45823416 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:30013025 | TATACACTGCTCTTT[A/G]CATAACCAATACCAC | 237711 |
rs45823490 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29756301 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGAAC | 237711 |
rs45851868 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29793903 | AGGCCACCGTGCTGC[A/T]GTGTGCACTGCTTCA | 237711 |
rs45900667 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29745848 | CATCTTTAAACTTAA[G/T]AAGATGTTATTAGCA | 237711 |
rs45987142 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29794009 | AATGGTAGCCTTATG[C/T]ACCAGGTCTCTGCAG | 237711 |
rs45999611 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29837036 | AACCTCACCTGTGAT[C/T]TTCCTGAATTCTGAA | 237711 |
rs46054180 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Eml6 | Mm_Celera | 11:29856987 | TTCATAAAGAAATTG[A/G]AAAGATCCTACACTA | 237711 |
rs46056595 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29753475 | CATAAGATACCGAGT[A/G]GGTGCTGGGAATTGA | 237711 |
rs46077344 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29757679 | TGCTGGGATTAAAGG[C/T]GTGCGCCACCATGCC | 237711 |
rs46085254 | snp | A/C/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29753815 | ACATCAGACTTGAAA[A/C/G]ACCAGGAGCTGCCTT | 237711 |
rs46115053 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29753927 | ATTATTCCTAGCATC[C/T]GCAAGGGTTGCCTAA | 237711 |
rs46160938 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29794753 | CTCAAGAAGCATTTG[A/G]TGAACTGTTATCTCT | 237711 |
rs46192031 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29753591 | GCCAAGCATTATCAG[A/T]CTGATCCAAATTAAG | 237711 |
rs46202099 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29755441 | TTATTTTCTTCTTTC[C/T]GCTCAAGATTCCCTG | 237711 |
rs46208063 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29756855 | GAATGCACACTATGC[C/T]CTTTACTGATAATAC | 237711 |
rs46226496 | snp | A/C | | | intron-variant | Eml6 | GRCm38.p3 | 11:29798123 | CTCACCTTGACTATT[A/C]TACTTCAGGACTTTT | 237711 |
rs46249097 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29753575 | TTTGCTGAGAGGATA[A/G]GCCAAGCATTATCAG | 237711 |
rs46251224 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29756869 | CTCTTTACTGATAAT[A/T]CAAATGTATATATGT | 237711 |
rs46364343 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29927383 | GGGGAGGGGCACAGT[A/G]TGGTCCTTTTCAGTT | 237711 |
rs46365981 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29768233 | TTGGTGACCACCCAC[C/T]TAAACATAAGCCTCA | 237711 |
rs46366024 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29745972 | CAGATTTCTTACCCT[G/T]TGCCTCTCGCCCCCC | 237711 |
rs46399562 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29773679 | GAGACTTTAAGTGCC[A/G]GGTGGGGCATTTGAA | 237711 |
rs46473115 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29755622 | CACTTGAAGAACAAC[C/T]CTGAACATCTTAACC | 237711 |
rs46474168 | snp | C/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29759740 | TAACTGTCAGGCTTT[C/G]AGACATGGGACTCAC | 237711 |
rs46493995 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29754701 | CTAAGGATAGGTAAC[A/T]CTGATTACTAAAAGC | 237711 |
rs46512187 | snp | A/C | | | intron-variant | Eml6 | GRCm38.p3 | 11:29796036 | TTATGAGTACACACT[A/C]TAAAGTGTAGGTGCC | 237711 |
rs46586683 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29798196 | CTTTGTCTTTTCCTA[A/G]ATCTAAGCTTATTCA | 237711 |
rs46621754 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29856930 | AACTTATGGGACATA[A/G]TGAAAGCAGTGCTAA | 237711 |
rs46677365 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29793756 | ATGCAAGTTAGTGGG[C/T]AAATGATTCAATTAT | 237711 |
rs46688700 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29754535 | GGCCAGCCATCCTAG[A/C]CTAACTAACAAACTT | 237711 |
rs46739204 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29798095 | TGACCCTGACACCCA[C/T]GTCTCTACCTAACTC | 237711 |
rs46773989 | snp | A/C/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29746439 | GCCCCACTTCCAGAA[A/C/G]CCCCCACTGCTCTGT | 237711 |
rs46782743 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29753931 | TTCCTAGCATCTGCA[A/G]GGGTTGCCTAAGCAG | 237711 |
rs46783486 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29792950 | ATTTGGGCACCTGCA[C/T]GCACATGTACATTCC | 237711 |
rs46931570 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836604 | AGACTCCTACATATT[C/T]TTATTAACCTTTCCC | 237711 |
rs46935351 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29837019 | ACCAGTAAGTGGCTT[C/T]TAACCTCACCTGTGA | 237711 |
rs46963855 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29798106 | CCCATGTCTCTACCT[A/G]ACTCACCTTGACTAT | 237711 |
rs46988910 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29927145 | GAATATTAGATTCCT[C/T]TTAATGATTTGCTTG | 237711 |
rs47049366 | snp | A/C | | | downstream-variant-500B, intron-variant | Rtn4, Eml6 | Mm_Celera | 11:29744710 | CCTACTCTCCTTCCC[A/C]GTCATCACTTGGGCT | 237711 |
rs47063416 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29779644 | TCAGGACAATAGCTG[A/C]CCAAAAGACAAAAGA | 237711 |
rs47075346 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29770957 | TTTGCTCCTGCTGGC[C/T]GATGAGACTCAAGGA | 237711 |
rs47134361 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29750895 | ACATGCACTCTAACA[C/T]GCATGAAGCCCTTGG | 237711 |
rs47141820 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:30019179 | AAAGACCAACATGCC[A/G]ACAAACTGGGAAAAC | 237711 |
rs47173227 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29746039 | AATCCCAGGAGAGCC[C/T]TAGAGGGGACACGGG | 237711 |
rs47209576 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29767829 | GTTGTAATGTAAATA[C/T]TCAATATGCAGAATA | 237711 |
rs47210659 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29753550 | TGGTCTCTCCAGCCA[C/G]ACTGGCTCCTTTGCT | 237711 |
rs47223705 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29793859 | GTGAGGCTATGTGGG[A/G]AGTTAGTGACAACCA | 237711 |
rs47231261 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29754718 | TGATTACTAAAAGCT[C/T]CTTAATCGAAAAAAG | 237711 |
rs47314441 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29769066 | ATTTTTTAACACTGC[C/T]AGTTATGAACATGTT | 237711 |
rs47320737 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29795195 | GTAAACAGACACCTT[C/T]ACCTGTGAGGAGATG | 237711 |
rs47321875 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29747055 | TTCACCACCAGGCAC[A/T]GCCCTTCCCCAACTC | 237711 |
rs47340778 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29768442 | GTGGGATGAAGTGAG[A/G]AAGGAGAATTGAGCA | 237711 |
rs47374637 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29799345 | GAATTGTCCACTGCT[A/G]GTTGCACCAGACAGA | 237711 |
rs47395426 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29796334 | CTATGTCCATACCTC[C/T]AGGCTCCCTACTGGG | 237711 |
rs47411392 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:30016830 | GTCCTGCAGCATGTG[A/C]CCATGACACCCCACA | 237711 |
rs47422643 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29756281 | GCGGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 237711 |
rs47481748 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29768785 | GGCCATGGAGCTCAG[A/G]AGGCTGCTCACTCAC | 237711 |
rs47496381 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29745605 | TGCAGACCTATGGGT[C/T]AGGTTGGAAGGGTTC | 237711 |
rs47572468 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29745028 | CCTCAAGGCCTTATG[C/T]TTTTAAGTTACTTTA | 237711 |
rs47572530 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29770426 | TGGGTACCATTCTTG[A/G]ATGAAAGCAAGCTGG | 237711 |
rs47584909 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29793302 | TCAAGAGGTAGAAGA[G/T]TTGAGATGACACAGT | 237711 |
rs47608309 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29758656 | ACAGTGTCTGGGTGG[A/G]AGGTGGTGATGATGC | 237711 |
rs47660581 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29745339 | AAATTTATTTGTAAT[A/G]GTTTAAAATTAATTT | 237711 |
rs47662914 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29754509 | AGGGAGATAGATCCC[G/T]GAGGGTCATTGGCCA | 237711 |
rs47674850 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29754302 | tcttagctattctgt[C/T]atagcaatgagaaaa | 237711 |
rs47677875 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29768638 | TTGGACTAAGGATTG[C/T]TGGAGAGAGGATTTA | 237711 |
rs47716936 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29754365 | CAATAACAACAACAA[C/T]GTGTAAAATGTAGTT | 237711 |
rs47756801 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29768803 | GCTGCTCACTCACAG[C/T]TGACATGATCTGATC | 237711 |
rs47800641 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29754697 | GATGCTAAGGATAGG[G/T]AACACTGATTACTAA | 237711 |
rs47810137 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29932683 | AAAAGACTTAGATTA[C/T]GTCTGAGATATGTGT | 237711 |
rs47825149 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836673 | ACTGCAAAACTTATG[A/G]ACTGTAGCATTCAAG | 237711 |
rs47825248 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:30017742 | GCAAGCTTTCACAAG[A/G]CTCAAAGGAATAGCA | 237711 |
rs47846528 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29790266 | ATAAAATGGCTGAAG[A/G]GTTTCATTCCCCTAG | 237711 |
rs47873326 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29798129 | TTGACTATTCTACTT[C/T]AGGACTTTTGGGATA | 237711 |
rs47939728 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29759297 | GACATTCTTGCAGAG[A/G]GAACTGGTGAGTTTC | 237711 |
rs48050024 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29746139 | TCGTGAAATTTCTTT[C/T]TTATTGTTCCATATC | 237711 |
rs48068923 | snp | G/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29790919 | CAATGAAAATAACCT[G/T]CAGATACCCAGTGCC | 237711 |
rs48112200 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29769064 | ATATTTTTTAACACT[C/G]CCAGTTATGAACATG | 237711 |
rs48152431 | snp | C/T | | | downstream-variant-500B, intron-variant | Rtn4, Eml6 | Mm_Celera | 11:29744713 | ACTCTCCTTCCCCGT[C/T]ATCACTTGGGCTTTT | 237711 |
rs48203466 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29745466 | ACCCCTGAGTTTTTA[A/T]TAAACAAAAACAATA | 237711 |
rs48251858 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29793896 | AGGCATGAGGCCACC[G/T]TGCTGCAGTGTGCAC | 237711 |
rs48347999 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:30018321 | TAATAGAAAAAAATA[A/G]ACAAGTTAGCCTTGG | 237711 |
rs48438430 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29793308 | GGTAGAAGATTTGAG[A/T]TGACACAGTCCAAGC | 237711 |
rs48439646 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29794516 | TAAAGCTCAGAACTT[G/T]CGAGGACACCTGCAG | 237711 |
rs48491750 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29793929 | CTTCACTACTCACTA[A/G]GTAGATGATGCTGGA | 237711 |
rs48496341 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29751712 | TGCTGAGGCCTCTTG[C/T]GAAGGGCTGCATGTC | 237711 |
rs48503341 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29932614 | GTCTGCTAATATCTT[C/T]ACCAGAGTTGTCTGG | 237711 |
rs48533125 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29932780 | AAAACATACTAAATA[G/T]TTGCAATTTTGAAAT | 237711 |
rs48568465 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29760502 | TCTGAAAGAGGGGCG[A/G]GGTGCTGAAAAGAAC | 237711 |
rs48630092 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29759306 | GCAGAGGGAACTGGT[A/G]AGTTTCTATTTGTAT | 237711 |
rs48639686 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29754728 | AAGCTTCTTAATCGA[A/C]AAAAGTAGAAGTGGC | 237711 |
rs48651181 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29759968 | CTGAAAGTGTTCATA[A/G]ACCAGTGGTCTATAT | 237711 |
rs48686523 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29759962 | CATCTCCTGAAAGTG[C/T]TCATAAACCAGTGGT | 237711 |
rs48709791 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29797886 | AAGAAACCCAACAGG[A/T]CCTATCTCCTGGTTC | 237711 |
rs48864304 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29753681 | TGCTAATTTGTTTGG[A/G]CATTTTTGTATCCCT | 237711 |
rs48999303 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29803435 | TGTTGTCTGGATGTA[C/T]ATATATATGCATTAT | 237711 |
rs49031406 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29796768 | CTCTAACCATCCCAC[A/G]GGGAGGGACATCACT | 237711 |
rs49037761 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29932662 | AAGCCTACAAGTAGA[C/T]GATGTAAAAGACTTA | 237711 |
rs49040193 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29799344 | GGAATTGTCCACTGC[C/T]GGTTGCACCAGACAG | 237711 |
rs49042473 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29751634 | TTATGTGTTTTGTCA[C/T]AGTTTAAAAATAATT | 237711 |
rs49046533 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29793506 | ACTGTAGTGAGACAG[C/T]GAAAAGACCAGCTAG | 237711 |
rs49135660 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29798115 | CTACCTAACTCACCT[C/T]GACTATTCTACTTCA | 237711 |
rs49141904 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29758915 | CCCTGTAGAAGCAGC[A/G]TGAAGCCCAGCGTGT | 237711 |
rs49186390 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29753574 | CTTTGCTGAGAGGAT[A/C]GGCCAAGCATTATCA | 237711 |
rs49230138 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:30018452 | CAGGCCCTACTCTTG[A/G]TCTACTCTCAAGTCC | 237711 |
rs49239271 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29776516 | AAGCCCACTGTCTAT[G/T]CAACAGTGTTCAGGG | 237711 |
rs49301377 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29754214 | TTATGCTATGCCATA[A/G]TGTCTCTCCTGTCAT | 237711 |
rs49337581 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836998 | TCTTGAGTCCTGACA[C/T]TGGAGACCAGTAAGT | 237711 |
rs49362879 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29799820 | ACAAAAGGGCTCAGT[C/T]TCTGATCTCTGTGAG | 237711 |
rs49363397 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29792148 | TTCACCTCCAGGAAC[A/T]TAAGATTTTGAGGTG | 237711 |
rs49437667 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29798004 | ggacttatttctcag[G/T]cctagatctcaagga | 237711 |
rs49469742 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29745511 | AAAACCTTTAAATAT[A/G]TTGAAATTGAGTTAT | 237711 |
rs49494446 | snp | C/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29746455 | CCCCCACTGCTCTGT[C/G]TGCAGAAGGCCTTGA | 237711 |
rs49506002 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29790238 | ACTTTTCTGTTGCTC[C/T]TTCACTTCCAACATA | 237711 |
rs49518348 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29770365 | TACAGGTTCTTTTTC[C/T]ATAATCCCTGCTAAG | 237711 |
rs49518984 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836829 | TTCTCACAGGGTTAT[A/G]TTTTATTCATGGGCA | 237711 |
rs49519371 | snp | A/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29793862 | AGGCTATGTGGGGAG[A/T]TAGTGACAACCAGTG | 237711 |
rs49523321 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29746113 | GAAATTTTTGGTTTT[C/T]CCCTAAAAACTCGTG | 237711 |
rs49569417 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29792728 | CAACATAATAAATGT[A/G]TATTTTTAAATCTTT | 237711 |
rs49594987 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29746136 | AACTCGTGAAATTTC[G/T]TTCTTATTGTTCCAT | 237711 |
rs49617653 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29793415 | TGTAAAGCTAGTAAC[C/T]TGGAACTGGCTTATG | 237711 |
rs49666421 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29985618 | TAGTGAGATGGCTCA[A/G]CAGGTAAAATGTTTG | 237711 |
rs49736266 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29855656 | AGAAAAGAAAATCCT[A/C]TCATCACATAATAAT | 237711 |
rs49812001 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29768432 | TTTTCAGACTGTGGG[A/G]TGAAGTGAGAAAGGA | 237711 |
rs49832258 | snp | A/G | | | utr-variant-3-prime | Rtn4, Eml6 | Mm_Celera | 11:29744152 | ATACATGGCTCATTT[A/G]GTTTTGAAAGCTAAA | 237711 |
rs49836478 | snp | A/C | | | intron-variant | Eml6 | GRCm38.p3 | 11:29760322 | CACATGCTCTGATGT[A/C]GGTCTGGAAGGACAA | 237711 |
rs49973103 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29753635 | CAGAGAACATGGAAC[A/T]TGAGACAGTCACCTG | 237711 |
rs50019229 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29798189 | TCTGACTCTTTGTCT[C/T]TTCCTAGATCTAAGC | 237711 |
rs50081839 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29746701 | ATCCATGATAACTGA[A/G]GGTCATCTATATGAC | 237711 |
rs50123685 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29753620 | AGCCAAACAGATTTG[C/T]AGAGAACATGGAACA | 237711 |
rs50130789 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29768965 | TCTCCAAACATAGCA[C/T]AAAAGCTTAGGGGAA | 237711 |
rs50161322 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29745673 | GGCCAAATAACCTGC[A/G]TATTTCACCTGACGG | 237711 |
rs50227411 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29748215 | AGAAATGAACATACT[A/G]TATCTATCCAAAAGC | 237711 |
rs50252721 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29754331 | aagtaaTACTTTTGA[A/T]TCAACATTTTGAGAA | 237711 |
rs50344283 | snp | C/T | | | synonymous-codon | Eml6 | GRCm38.p3 | 11:29754920 | GACCCCTTTCTTGTA[C/T]AGCAGAGCACTTCCT | 237711 |
rs50433673 | snp | C/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:30018739 | GGTACATTAAAAACC[C/G]TTGGCCCTCCTAGAG | 237711 |
rs50457505 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:30014683 | AGAATCTAGTGGTCA[A/G]GGAACTCCTAGGGGT | 237711 |
rs50472716 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29756228 | CCGGGTGGTGGTGGT[A/G]CACGCCTTTAATCCC | 237711 |
rs50475947 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29754451 | AAATTTTAAAAAGCC[C/T]GGTGTGGTATGTGCT | 237711 |
rs50481334 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836423 | TTGGTTGTGAGGTCT[A/G]TTTGCTCACAATAGA | 237711 |
rs50536297 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29755327 | GCTTCTAGACAGGTA[G/T]AATTGATCATGCCCA | 237711 |
rs50544358 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29985555 | AGTGATACCTACAGA[A/G]AAAACACTGATTTCC | 237711 |
rs50610467 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29768893 | GCTACTGATTAAAAG[A/C]GACACTTTTTTTTTT | 237711 |
rs50617400 | snp | A/C | | | intron-variant | Eml6 | GRCm38.p3 | 11:29759462 | ATGACAATGAAGAAG[A/C]ATCAAGGGAAACAAT | 237711 |
rs50720990 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29794011 | TGGTAGCCTTATGCA[C/T]CAGGTCTCTGCAGAA | 237711 |
rs50722547 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29769642 | AGCTACCTATATGGT[A/G]GTACTATGATAATTA | 237711 |
rs50754721 | snp | G/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29837014 | TGGAGACCAGTAAGT[G/T]GCTTCTAACCTCACC | 237711 |
rs50767789 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29757518 | CAAGGCTGTAAGGTA[A/G]GAAACTCCACTTCTT | 237711 |
rs50885966 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836959 | AGATACAGAGAAGAT[A/G]CCAACTCTCACTGAC | 237711 |
rs50898865 | snp | A/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29933055 | ATTTTGCTTTAAAAT[A/T]GTAAGGGGAGCTAGC | 237711 |
rs50949002 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29768020 | CACAATGGTAGTAGC[C/T]AGGCTTCTCCCGCAC | 237711 |
rs50956553 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29750977 | AGTCAGAAGGTTCCA[A/T]GTCTTCCTTTATTTC | 237711 |
rs50984362 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836835 | CAGGGTTATGTTTTA[C/T]TCATGGGCATTTAAT | 237711 |
rs50997403 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29789380 | CTCAAGACAGAGTAG[A/T]TTTTAGAGATCACAT | 237711 |
rs51083515 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29789689 | TCCTACCGACCATGA[A/G]ATCCACCTTCTCCAT | 237711 |
rs51103111 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29768474 | AGGGAGAAAAGACTC[A/G]GCCTGCTTATGTAAA | 237711 |
rs51121520 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29789148 | TCTGGGTCTCTGCTA[C/T]CAAAAGCTAGGCTGG | 237711 |
rs51185892 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29753835 | GGAGCTGCCTTACAT[A/G]TATGCCAGAAGTTTC | 237711 |
rs51238139 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29927487 | TGAGTCATGCTGTCT[A/T]TATCAAATTTTAAGA | 237711 |
rs51296630 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836534 | CAATGAAAACCATTT[A/G]ATAATGGTATCCTGA | 237711 |
rs51316957 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29759361 | GCAAATGACACATTG[A/G]CATGACCTTGCTGTG | 237711 |
rs51344802 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29793871 | GGGGAGTTAGTGACA[A/G]CCAGTGTGCAGGCAT | 237711 |
rs51411199 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29753998 | CTTCATGGTTGCTCG[A/C]TGTCAGTTTGGATGG | 237711 |
rs51411575 | snp | C/T | | | synonymous-codon | Eml6 | GRCm38.p3 | 11:29754938 | CAGAGCACTTCCTGC[C/T]AGAGTCCAGAACTTC | 237711 |
rs51412391 | snp | G/T | | | downstream-variant-500B, intron-variant | Rtn4, Eml6 | Mm_Celera | 11:29744732 | ACTTGGGCTTTTTTT[G/T]TTTTTTTTTAAGGTT | 237711 |
rs51437146 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29746125 | TTTCCCCTAAAAACT[C/T]GTGAAATTTCTTTCT | 237711 |
rs51460651 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29754408 | TGCCTTTGCAAGAAC[A/G]AGGTCTTGAGTTCAA | 237711 |
rs51472169 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29753583 | GAGGATAGGCCAAGC[A/C]TTATCAGTCTGATCC | 237711 |
rs51483552 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29745372 | TGCCTGTACACATAC[A/G]CGTGCAAGCTCAATT | 237711 |
rs51488056 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836961 | ATACAGAGAAGATGC[C/T]AACTCTCACTGACTT | 237711 |
rs51517136 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29754648 | GCACACTGACAAACA[C/G]ACATGTGCACATGTT | 237711 |
rs51525256 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29753863 | TTCTACTGAGGTATT[G/T]GTGGAGGAGGGGGCC | 237711 |
rs51549433 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29798187 | CTTCTGACTCTTTGT[C/T]TTTTCCTAGATCTAA | 237711 |
rs51609210 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29759537 | CCCAGAAGACTCCAA[A/G]TGATGGATTAAAATG | 237711 |
rs51609252 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29753858 | GAAGTTTCTACTGAG[C/G]TATTGGTGGAGGAGG | 237711 |
rs51624820 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29745374 | CCTGTACACATACAC[A/G]TGCAAGCTCAATTTC | 237711 |
rs51628755 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29751551 | AATATTTGAAGGTGA[C/T]GGTGGTAGTGGTTGC | 237711 |
rs51658939 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29836667 | GGCAAAACTGCAAAA[C/T]TTATGGACTGTAGCA | 237711 |
rs51675309 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29754839 | GAGGAAGTATCTGTT[A/G]GAACTCACAGCACCA | 237711 |
rs51715263 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29755623 | ACTTGAAGAACAACC[C/T]TGAACATCTTAACCT | 237711 |
rs51754303 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29791373 | TCTTATATTCTTTCA[A/G]AACTAGCCCATTTCC | 237711 |
rs51770924 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29759755 | GAGACATGGGACTCA[C/T]TTACATCTAAGGGTC | 237711 |
rs51833584 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29768724 | TTGCAACAATACAAG[C/T]TTAGAGAGCAGCTAT | 237711 |
rs51892430 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29769485 | AGTAAAAGCAATGCT[A/G]ACAAAGATGGAGGAC | 237711 |
rs51992389 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:30014742 | TGACTCCCTTTGATC[A/G]ATCACTGATTAACAC | 237711 |
rs52003945 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29768457 | AAAGGAGAATTGAGC[A/C]CAGGGAGAAAAGACT | 237711 |
rs52106300 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29866749 | GAGAGAGAGAGAGAG[A/G]GAGAGAGAGAGAGAG | 237711 |
rs52153679 | snp | A/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29787880 | TAAAAACAATTTTTT[A/T]AAAAAGAAAACCATA | 237711 |
rs52171705 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29753406 | GGCACATAAGTATAA[G/T]TACCTATAGAAGCCA | 237711 |
rs52181101 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29779405 | TGTTCTCATACTTTT[A/T]AAAATAATAAAAATG | 237711 |
rs52236572 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29779423 | AATAATAAAAATGAA[C/T]CAGAGAGGAAGACAG | 237711 |
rs52377598 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29753405 | AGGCACATAAGTATA[A/G]TTACCTATAGAAGCC | 237711 |
rs52455945 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29866753 | GAGAGAGAGAGGGAG[A/G]GAGAGAGAGAGAGAG | 237711 |
rs52675657 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29913702 | CCCCTTTTATAGTGG[G/T]CTAGGCTACCTTGCA | 237711 |
rs107607838 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29873068 | TGATTGCAAGCTCAG[A/G]ATTCTTAACTCACCA | 237711 |
rs107620666 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29858551 | TTGCAGGCAAATGGA[C/T]GGAACTAGGAAATAT | 237711 |
rs107845482 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29787561 | CGATCAGCTGGCCAC[C/T]CCTCCACAAGAAGCA | 237711 |
rs107910789 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29858719 | GTGGATAACTCAAAT[A/C]CACTTAGAAGGGGGA | 237711 |
rs107916871 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29858985 | ATGCCCAACAGTGGG[C/G]AGATCGAACCTGAAA | 237711 |
rs108063708 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29846667 | ACACAAACACACAAG[A/G]TATATAGTCACTGAT | 237711 |
rs108115906 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29756227 | GCCGGGTGGTGGTGG[C/T]GCACGCCTTTAATCC | 237711 |
rs108149762 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29873379 | CTTGCTGTGGCCATC[C/T]GGCCATACAAAGCAA | 237711 |
rs108159774 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29926186 | CTGGCCCCTCCCTGG[C/T]TTTCCTCTACTCCTT | 237711 |
rs108345952 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29873470 | GTTTGGTTATGGTTG[A/C]TGCCTTACAGGGGAC | 237711 |
rs108384161 | snp | G/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29747972 | GAGTTCATGGAAAGA[G/T]CCTAAATCTTTCCCA | 237711 |
rs108449929 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29787508 | GGGAGTTAGAGATTC[A/G]AGAGAGGCAAGCCCG | 237711 |
rs108574656 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29858834 | ATGTGGGGAAACAGG[A/G]GAGAAGCCTAGAGGG | 237711 |
rs108711355 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29846696 | ATAAGTGGTTATTAG[A/G]CAAAGAGCTTAGAAT | 237711 |
rs108804980 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29855669 | TCCTCATGATATAAT[A/C]ATTAAAACACTAAAT | 237711 |
rs211694559 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29860250 | GCACCTGCTGAGCCT[C/T]TACACCAGTTGAGCT | 237711 |
rs211716044 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29917357 | ATAAGAATGAACCAT[A/G]AAGAAAATGAAATAC | 237711 |
rs211722915 | snp | A/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29788741 | ACTATATGAACCAAA[A/T]CAATGCCAGGCCATT | 237711 |
rs211724230 | snp | C/G | | | intron-variant, upstream-variant-2KB | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29826819 | CACTCTTCCTGCTAC[C/G]AGCCTGCGGAAGCTC | 237711 |
rs211735649 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29991325 | GAGGGACCTATGACT[A/T]CAGGGGCATATGTAG | 237711 |
rs211740204 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29973739 | GCATACAACTCACCA[A/G]CTATGTTAGTCTTGC | 237711 |
rs211742224 | snp | A/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29760295 | GGGACTGTTTAAAAA[A/T]AATAATAAAATCACA | 237711 |
rs211754409 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29918333 | GAGCAGAGACATCCC[C/T]GCAACCCTCCCCTAT | 237711 |
rs211754966 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29910073 | GAAAACCCAAAGCTG[A/G]CTTGATTTGAACACC | 237711 |
rs211755302 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29853636 | TGCTCGTGTGTTGAA[A/G]ACAACTTTAAAATCA | 237711 |
rs211757752 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29861013 | GAGCTGTGAGGATCC[A/C]TGGAGATTGCCAGAC | 237711 |
rs211772318 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | Mm_Celera | 11:29807960 | CTGCAGATTTCTTGT[C/T]TTTGGAATGAACATA | 237711 |
rs211777020 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29959981 | TTCTGTCAAGCCCCT[C/T]TTATTGTGACACAGC | 237711 |
rs211797564 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29789876 | GCCTGCTATCATCTG[C/T]CTTAAGGGAATTCTG | 237711 |
rs211802076 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29815415 | TGAGCTGCAGGAGAC[A/G]GGAGAGGCACATTAT | 237711 |
rs211805606 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29998059 | TCTTAGCCATTCTGA[C/T]TGGTGTAAGGTGGAA | 237711 |
rs211808583 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29753322 | TCTTTATTTTGAATT[A/G]TGCATTTGTATGTGT | 237711 |
rs211813804 | in-del | -/A | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29829291 | TTGCACTGGTGTCAG[-/A]AAAAATGTCCACAAC | 237711 |
rs211816790 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29865971 | ATCAAAATAGCTTAG[C/T]ATGACTCTGTCATGT | 237711 |
rs211819311 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29974961 | TGAGTACCAAGATTA[C/T]AAAGCAGGGCCACTA | 237711 |
rs211843833 | snp | C/T | | | intron-variant, utr-variant-3-prime | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29823009 | AAATGAGGAGCCTTC[C/T]CAGGACCTTGGTCAC | 237711 |
rs211845636 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29990005 | ACAGAACAGCAATAG[C/T]TTGTGCTGTAAGATC | 237711 |
rs211858132 | in-del | -/ATGTATATGTATATGTATATGCATATGTATACACACACAC | | | intron-variant | Eml6 | GRCm38.p3 | 11:29803212 | TATATGTATATGTAT[lengthTooLong]ACACACACACACACA | 237711 |
rs211883591 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29759488 | ACAATAGCAAAGTAA[A/G]TCTTGTTCCTATCAG | 237711 |
rs211885265 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29926460 | CAGTTATTAGTTTTC[A/T]GTGAAACGGGGTCCA | 237711 |
rs211885372 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Eml6, 4931440F15Rik, LOC105243970 | GRCm38.p3 | 11:29822742 | TTATTGGGATACTGG[A/G]GACTCCTCAATACAA | 237711 |
rs211894397 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29952082 | TAAAGCCATGAAGGC[A/C]AAAAGCTCTATACAA | 237711 |
rs211938953 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29815758 | AAACCCAGCCCAGCA[C/T]CACTGACTGTCTGAC | 237711 |
rs211945066 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29923965 | AAAAAAAACCCAAAA[C/T]AGGAAGCCAGCTATG | 237711 |
rs211953616 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:30013697 | TGGCTGCTGAAGGTA[C/T]GTAGTGCATGGACTG | 237711 |
rs211966966 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29896374 | GGCTGCAAAGCTCCT[C/T]ATGGGTGTTACACAT | 237711 |
rs211969997 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29866640 | GATGCCAGAGTCATG[A/G]GATACCTGTCAAGGA | 237711 |
rs211980283 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29943179 | GTTGGAAGACTAAAT[A/G]TATATATGTATATAT | 237711 |
rs211990600 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29753592 | CCAAGCATTATCAGT[A/C]TGATCCAAATTAAGC | 237711 |
rs212004860 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29745706 | AAAAGCTGCCTTGGC[A/T]CTTTGTCCAAATAGC | 237711 |
rs212011054 | in-del | -/A | | | intron-variant | Eml6 | Mm_Celera | 11:29745464 | TACCCCTGAGTTTTT[-/A]ATTAAACAAAAACAA | 237711 |
rs212016387 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:30019999 | TGAAGAACACTGAAG[C/T]AATAGCTGTGGGCTT | 237711 |
rs212022497 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29904318 | TAACAGTTAAAACCC[A/G]CAGAGTCCACACAGC | 237711 |
rs212031552 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29799603 | TGTTTCATAAAATCT[A/G]TCACTGCCTCTTGTA | 237711 |
rs212042112 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29848432 | TTAGAAACTTGCTAT[A/G]GCATTGGTTCTTGCA | 237711 |
rs212046846 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29800353 | TCCCTCTAAATGTCA[A/G]GACCCTTCAAGGTAA | 237711 |
rs212049478 | snp | A/C | | | intron-variant | Eml6 | GRCm38.p3 | 11:30014788 | ATCTGTAAGTCGCCT[A/C]GTCTGTTACCTCTGG | 237711 |
rs212051229 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29847591 | AGAGGGGATAGGATA[A/G]GATAGGGCATTTGCA | 237711 |
rs212061861 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29840754 | GCCAAAGTCAATACC[A/C]TGAGAAGGCCTGATG | 237711 |
rs212068449 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29854033 | CAGGAAGTCCATGAG[C/G]GTATGGTGGAGCCTC | 237711 |
rs212075546 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:30023587 | CTGGGAAGAAACATG[C/T]CTAGTCTAGACAAGA | 237711 |
rs212097308 | in-del | -/TAT | | | intron-variant | Eml6 | Mm_Celera | 11:29949842 | CATGACAGAGCCAAG[-/TAT]TTTTTTCATGAAAAT | 237711 |
rs212117509 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29769930 | GATCTCAGAGAACAC[C/T]TGCATAGTCACATGC | 237711 |
rs212126306 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29834257 | CTGAAACCATTGTCA[C/T]GGATAATTAAGCCCT | 237711 |
rs212136256 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29999524 | CCATGATTTTAGTAG[A/G]ATTGCTTATATCTGT | 237711 |
rs212136364 | snp | C/T | | | intron-variant, upstream-variant-2KB | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29826248 | TTACTGCCCTTCCTG[C/T]CCCCTATGAATGTAG | 237711 |
rs212155300 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29770374 | TTTTTCCATAATCCC[C/T]GCTAAGACTAATTCT | 237711 |
rs212159137 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:30006512 | GCAAGAGAGGATGGG[A/G]AGGCAAGCCCTCTCA | 237711 |
rs212164644 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29841314 | CCTAGTCTGCAACCT[G/T]ACACACTATGGTTGA | 237711 |
rs212177496 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29934001 | CAGGAAATTTAAGCA[C/T]ACTGACTGACTACAG | 237711 |
rs212199869 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29875393 | CTTTGGGAAGAGAAG[A/T]ATATGTGATTGGATC | 237711 |
rs212200674 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29896962 | ATTCTGTTCTATTTT[C/G]AGTTTATAATAAATC | 237711 |
rs212210248 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29910624 | GACTTTAATGCTACG[C/T]TCTCTGGTCGAGTCA | 237711 |
rs212231070 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29884067 | AGGGCAGGCAGCTCA[C/T]GGAGCTTAAGAGCTG | 237711 |
rs212231626 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29784814 | AGTAGATAAAAAAAT[A/T]TTTTCTTACATTTGG | 237711 |
rs212232357 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29833265 | TTTCTAATCATTCTT[C/T]TAAAAAGCAATCACA | 237711 |
rs212236362 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29960621 | CCTTGGAGAGTGAGA[G/T]CTTGAATGAATAGGG | 237711 |
rs212241356 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29943796 | TTCCTTTTTTATCAC[A/T]TCTATATTTACTTCA | 237711 |
rs212244944 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29884687 | AATTACTGGACTAGG[A/G]AGGATTGGCATTTCT | 237711 |
rs212256969 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29904659 | CACGCTCTCTTACAA[A/C]AGCAGAAGATGGCAC | 237711 |
rs212273733 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29762990 | ATACCAGTTGTATTT[A/C]CTAACTTGAGCTATC | 237711 |
rs212284847 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29778432 | TAAAACTACCTATTC[C/T]TCCCAAAAGCACCAA | 237711 |
rs212291240 | in-del | -/T | | | intron-variant | Eml6 | Mm_Celera | 11:29936188 | AAACTTATCGCCAGG[-/T]CCTCAGCTCACCCTC | 237711 |
rs212292693 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29877066 | TCACCAAAAGCAAAT[C/T]TTGATTTTGTCTTAT | 237711 |
rs212294496 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29934386 | AGGGATATGGGTGGG[A/G]CACATAAACAAATAT | 237711 |
rs212309155 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29784911 | AATAGCTGTGGGAAT[C/T]ACTTGTCCCCTTGCA | 237711 |
rs212309996 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29862521 | CTGCAGTCCCACTTC[A/G]CAGCACTGTCTGGCT | 237711 |
rs212315642 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29854664 | GCCCAAATAACCACC[C/T]AAACTGGGACCCTCA | 237711 |
rs212330575 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29810741 | TTCAAATCTACTTGA[A/G]CCTCTTGAATTTTTA | 237711 |
rs212337772 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29927604 | CATGTACTATCTTCA[C/T]TTAAGCATAGTACCA | 237711 |
rs212358688 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29913036 | TCGAGTAGACTGCTG[C/T]AGGACCCCATGGAAC | 237711 |
rs212370273 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:30000225 | TTCCAGTTTTGTTGA[A/G]TAGAGGCTTTTGCAG | 237711 |
rs212373243 | in-del | -/TTTTG | | | intron-variant | Eml6 | Mm_Celera | 11:29768384 | TGAGAGCAAGGGTTT[-/TTTTG]TTGTTGTTGTTGTTT | 237711 |
rs212378535 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29855239 | AACAAAATGGTCCAA[A/G]ACCTAAAACTGGATA | 237711 |
rs212380212 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29747015 | GTAGGTCATTTGGTC[A/C]CGTGGGCACACCCTG | 237711 |
rs212412178 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:30014360 | TCCATAGTTACAGTA[A/C]AGTCTCTAAATGGTT | 237711 |
rs212434439 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29994085 | ATATCTCTCTCCTCT[C/T]TAAGCTACACTCTAA | 237711 |
rs212435471 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29868891 | ATGGCTATCTTATTG[C/T]TTTGTGCACCACACC | 237711 |
rs212441633 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29784027 | ATTAGGGTAACTAGC[A/G]GAACAGATGAAATCT | 237711 |
rs212456394 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29937660 | GTGGACTGCCCATGA[C/G]GGGTGCAGTGAACTA | 237711 |
rs212462892 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29879506 | CCCTCACTCTGCAAA[C/T]ACTCAAGAGGGTGGG | 237711 |
rs212471849 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29994581 | GGTGGCAGAGCGTCA[A/G]CTGTGCAGCTCTGCA | 237711 |
rs212472364 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29912301 | AGAGAGACCGGCCAT[A/G]GCCAAGAGGAGAGAA | 237711 |
rs212489024 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29912522 | GGGGCGGTAACTTCA[A/G]TAGGAGCCAGAGTTC | 237711 |
rs212497113 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29781277 | ATCAGAAGATTATTA[A/T]CAGAAATTTAGAAAC | 237711 |
rs212497146 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29773214 | CCCAACTTGAGACTC[A/G]TCCCATGGACAAGCA | 237711 |
rs212527061 | in-del | -/GC | | | intron-variant | Eml6 | GRCm38.p3 | 11:29766167 | AACCTGCATCAGGTA[-/GC]GTCTGCCCTTTTCAG | 237711 |
rs212543892 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:30003091 | TCACTTTAACATGTA[C/T]AAGGTGTTCAAAGGG | 237711 |
rs212544573 | snp | A/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29931808 | TGAGGAGAGAATGTG[A/T]GGTTTGTATGGAGTG | 237711 |
rs212556748 | in-del | -/C | | | intron-variant | Eml6 | Mm_Celera | 11:29851078 | CAAAACAAAACAAAA[-/C]AAAAACCAGAACAGA | 237711 |
rs212558893 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29773962 | CCCTTCCCACAGCTC[C/G]TGCTCTTCTCCTCCC | 237711 |
rs212561771 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:30018506 | AATCATGCAATCTAA[C/T]GTCTTATCTGATGAA | 237711 |
rs212569278 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29754606 | CCATAGTTGCCCTTT[G/T]GTATTCACACTTGCA | 237711 |
rs212575657 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29787079 | GGGGTGGGGCCGCAC[A/T]CAGCCTCTGAGGCTT | 237711 |
rs212589948 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29981620 | ATACTAAACCTGTGA[A/G]GGGAACAAGCTTGTT | 237711 |
rs212601916 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29829175 | GGAAGGGATGCCTTG[A/G]CATGGGCCCACTGAG | 237711 |
rs212603391 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29902130 | TCTTAAGTGATTCAA[A/C]ATTGTGTCTAGCTGA | 237711 |
rs212611571 | in-del | -/G | | | intron-variant | Eml6 | Mm_Celera | 11:29925354 | ACCAAGAAGCTAGTT[-/G]GGGGAGGAAAGGGTT | 237711 |
rs212633031 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29968251 | AAATAGTGGGGACAA[G/T]CTAGGGAAAGTTCTT | 237711 |
rs212638372 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29886715 | AAGCAACAGAGCTTC[C/T]TGGACAGGGTCCCTT | 237711 |
rs212651314 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:30010909 | TGCCTGGCCCCTGTG[C/T]AGTGCCTGAGAAGCA | 237711 |
rs212651723 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29888261 | GGAAGTAAAAATCAC[C/T]TTTCTTTAATATCTC | 237711 |
rs212661822 | in-del | -/AC | | | intron-variant | Eml6 | Mm_Celera | 11:29795682 | CACATAAGGATGATT[-/AC]ACAGTGTTTCTATTC | 237711 |
rs212666288 | in-del | -/GAA | | | intron-variant | Eml6 | Mm_Celera | 11:29796539 | GTGATCTGGAAGATG[-/GAA]GGAGGTTTCCTATGT | 237711 |
rs212671459 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29817092 | TCAGAAAGGGAAACA[A/G]AATAGTCATCAGAGG | 237711 |
rs212683156 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29948547 | AGCAGTATGATACAC[C/T]GAGAGGTAGTAGAAA | 237711 |
rs212685967 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29780581 | CCCTGGTTTGCAAGG[A/T]CACAAACACATTCAT | 237711 |
rs212686597 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29757807 | GGGGACACTTGAAGA[C/T]AGTGAACTGTCAACA | 237711 |
rs212688741 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29868377 | AGGACACAAGTGTCA[C/T]ACCACAGAGAAATTA | 237711 |
rs212698902 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29986213 | TATGTTATACGATGG[A/G]AGGTCAAGAATAGGA | 237711 |
rs212703093 | in-del | -/TAA | | | intron-variant | Eml6 | Mm_Celera | 11:29884031 | GTAAGAATGCCTTTT[-/TAA]TAATATCTGTCTGGG | 237711 |
rs212716280 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29915062 | ATTTAGACATGGCAG[G/T]AGGCTATGCATTGTA | 237711 |
rs212716720 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29857714 | ATCACTCAAAGAAGT[C/T]AGGACTGGAACTCAA | 237711 |
rs212717661 | snp | A/C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29925128 | ACACACACACACACA[A/C/G]AACCCTGTCTCAAAA | 237711 |
rs212720163 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29865321 | GCACTATTTGAGGGT[A/G]TGCCCTAGCTGGAGG | 237711 |
rs212735064 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29970677 | TGTAGGTAATGGTAG[A/G]TACTATAGGAACTAA | 237711 |
rs212746755 | in-del | -/CAC | | | intron-variant | Eml6 | Mm_Celera | 11:29853889 | AAAAAAAGATAACAA[-/CAC]CAACACTCTAAGAAG | 237711 |
rs212753510 | snp | A/T | | | intron-variant, upstream-variant-2KB | Eml6, LOC105243970 | Mm_Celera | 11:29820283 | TCAGCCTGTGGGTTG[A/T]AACCACTTTAAGAAG | 237711 |
rs212755357 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29809909 | CAATTCAAAGGAAAT[A/G]TGTTTACTATAGACA | 237711 |
rs212762811 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29794681 | AATCTTGTCTGTATC[G/T]GATTCTAAAGACGAG | 237711 |
rs212784352 | snp | C/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29871441 | ACAGTCAATGTTAAT[C/G]GTTAGCTCTTTAAGT | 237711 |
rs212785658 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29762089 | GTCCCATAAGCAGCT[A/G]TGACTGCTGTCAAGG | 237711 |
rs212787105 | in-del | -/AC | | | intron-variant | Eml6 | Mm_Celera | 11:30016104 | TGATGAAGGAGTTCT[-/AC]ATCTTTATCCAAAAG | 237711 |
rs212819157 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29828606 | TTCCCTCTGACCTAT[C/T]CTCAGATGGCTCCAC | 237711 |
rs212835259 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29996256 | CCCGTGTCTGAAGCA[A/T]ACATATGTATGTTCT | 237711 |
rs212838761 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:30003697 | TACTGTAACGCATTG[C/T]ATGGTATGCCCTATA | 237711 |
rs212838776 | in-del | -/AAA | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29837590 | CCCAATTTCTCTTTC[-/AAA]AAAAAAAAAAATCAC | 237711 |
rs212854429 | in-del | -/TTTTTTTTTTTT | | | intron-variant | Eml6 | Mm_Celera | 11:29960031 | GTCGACGAAAAAGGC[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTA | 237711 |
rs212862063 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29813651 | AATCATCTTCCATAC[C/T]TCCCCCTAAAGAGTC | 237711 |
rs212872675 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29996616 | CCTGTCCCAGTCCCT[C/T]GCCCCCAGTTCCTCA | 237711 |
rs212874918 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29788663 | AGCCTGGTTGCCACA[C/T]CATACTATGGTTGTA | 237711 |
rs212884203 | in-del | -/A | | | intron-variant, downstream-variant-500B | Eml6, 4931440F15Rik, LOC105243970 | Mm_Celera | 11:29822095 | GATTCAGATATTTGC[-/A]AAAATGAGAGCTTCC | 237711 |
rs212890184 | snp | G/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29846705 | TATTAGGCAAAGAGC[G/T]TGGAATACCCATGAC | 237711 |
rs212890651 | in-del | -/CT | | | intron-variant | Eml6 | Mm_Celera | 11:29868160 | GAGAGAAGTAGCCTA[-/CT]CTCTGCACATAAGCC | 237711 |
rs212893501 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29846437 | CTCCAACATGTAATA[A/C]GAACACATGCTCCAC | 237711 |
rs212896416 | in-del | -/CA | | | intron-variant | Eml6 | Mm_Celera | 11:29934321 | GTGTGTACATGCATG[-/CA]TACACACACACACAC | 237711 |
rs212903240 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29949701 | GGGAAGCCACAGAGC[C/T]AGGACTCAGATCCAG | 237711 |
rs212903364 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29958585 | CTCTGGAATGTGTAT[A/G]GACACTAATCACCTC | 237711 |
rs212905923 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29864393 | ATGCACATATGTGCA[C/T]AGTGTCACAAAGACT | 237711 |
rs212908146 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29950141 | GGTGTGCGCCACCAC[A/G]CCCGGCGCGGCTCAT | 237711 |
rs212948552 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29839014 | CCTTGGCCAAGCTTG[C/T]CTTAAACTTGATTTT | 237711 |
rs212950679 | snp | G/T | | | intron-variant | Eml6, LOC105243970 | GRCm38.p3 | 11:29835980 | TTATTTTTCTCCCTC[G/T]AGTCCTAATCCAGTC | 237711 |
rs212951451 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29844770 | TCACCATGACCAAGG[C/G]TTCATCCCAGGGTTG | 237711 |
rs212964260 | snp | C/G | | | utr-variant-3-prime | Rtn4, Eml6 | Mm_Celera | 11:29743937 | CTGCTCACCTTATAA[C/G]TGCTTTCCTAGAGCA | 237711 |
rs212968593 | in-del | -/G | | | intron-variant | Eml6 | Mm_Celera | 11:29895605 | GGTAACAACAATGAA[-/G]AATATTTTCAACTTT | 237711 |
rs212971010 | in-del | -/TTTTTT | | | intron-variant | Eml6 | Mm_Celera | 11:29995150 | AATTCACCGCTTCAG[-/TTTTTT]TTTTTTTTCTGGGTA | 237711 |
rs212986172 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:30020486 | ATGTAACCTCAACAA[C/T]ACTACAAATACTATA | 237711 |
rs212988448 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29879082 | AATTAGAACATGACC[A/T]TTAAAATGTTCTTGC | 237711 |
rs212991988 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29950567 | CACACATATTCCCCA[G/T]ACTTCTGCTTGAATG | 237711 |
rs212993074 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29893094 | AGCGGGGGGGGGGGG[A/G]GTTTATAGGGGGCTT | 237711 |
rs213003999 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29908739 | TTTTAAATACAAAAA[A/T]TACATTTTAAAATAA | 237711 |
rs213009095 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29936695 | TGAGGATTATACTTG[C/T]CATGTAAGAATGTTT | 237711 |
rs213027351 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29750994 | TCTTCCTTTATTTCA[A/T]ATTGAGCTCAAGCTA | 237711 |
rs213037193 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29852267 | TACAAACAACAGCTT[C/G]TTTGTTAGTTGTAGT | 237711 |
rs213041046 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29805866 | TGGATGAAAGTGTTG[A/T]TAGAGTTATATTAAA | 237711 |
rs213048718 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29903047 | TGTGGAGTTAGTGGG[A/G]CAAGCTCTCAGGGTC | 237711 |
rs213057673 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29797012 | TTACCAATCTTACCA[A/G]ACCCTTTAGTTGCAT | 237711 |
rs213070769 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29957815 | GTGAGCAGGGGGAGG[G/T]GGGAGGGGATAGAGA | 237711 |
rs213074038 | in-del | -/C | | | intron-variant | Eml6 | Mm_Celera | 11:30022587 | GCTACTGTTCCCCTT[-/C]CCCCCAAAGGATTAT | 237711 |
rs213075621 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29872880 | CATGTGAGAATTGGC[A/G]GTCGAACTTTGTAAT | 237711 |
rs213075947 | in-del | -/ACAGTC | | | intron-variant | Eml6 | Mm_Celera | 11:30008168 | TAACTGAGGCCCAGA[-/ACAGTC]ACAGGCTTGGTGATA | 237711 |
rs213078870 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29932681 | GTAAAAGACTTAGAT[G/T]ACGTCTGAGATATGT | 237711 |
rs213080398 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29767370 | CAAAGATAGGATCCT[A/G]CGATTCCATGAACCC | 237711 |
rs213101866 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29760733 | TAAAACCTACTCACg[G/T]gctggtgagatggct | 237711 |
rs213102247 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:30019966 | TGGGAGGAACCACAG[A/T]GACTAAGAACAGGAG | 237711 |
rs213105590 | in-del | -/TC | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29817281 | TGGAGGGGGGGCATT[-/TC]TGAGACTAGCTGGAG | 237711 |
rs213122843 | in-del | -/CCC | | | intron-variant | Eml6 | Mm_Celera | 11:29957883 | ATTTGGCCCTTAACT[-/CCC]AGGCTTAAACATCTC | 237711 |
rs213123000 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29776041 | TAATATAGATGGAAG[A/G]GGAGAATTAGGGCTT | 237711 |
rs213125707 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29767163 | ATGAGCCACTGTGCA[A/C]GCTGAATAGAAAGTA | 237711 |
rs213134368 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29758495 | AGTGATTAAGGTGAA[C/T]CCTCATTTCAGAAGT | 237711 |
rs213136274 | snp | A/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29814205 | CCAGGAACAAAGGGA[A/T]GGATAAGAAAACTGG | 237711 |
rs213137274 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29882476 | GTAGATAAGTATAAA[A/G]AGAAAGCCACATCTA | 237711 |
rs213140749 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29997565 | CTTCTTGAGTTCTGT[A/G]GATTGTATCCTAGGT | 237711 |
rs213140848 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29831090 | GGCTTTTATTCTCTC[C/T]TTACTGACCTGGCGA | 237711 |
rs213158934 | in-del | -/AAG | | | intron-variant | Eml6 | Mm_Celera | 11:29946758 | CCCCAATGCTGCCTC[-/AAG]AAGAACTGACAAGAA | 237711 |
rs213163929 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:30012658 | AGAAAACAATAATAA[A/G]TAAATAAACTGAATA | 237711 |
rs213175522 | in-del | -/GTACG | | | intron-variant | Eml6 | Mm_Celera | 11:29886255 | ACTCAGCAGTTAAGA[-/GTACG]GTCTGCTCTTCCAGA | 237711 |
rs213180699 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29768427 | GTTTGTTTTCAGACT[C/G]TGGGATGAAGTGAGA | 237711 |
rs213186047 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29776772 | AGGCTCCCTTGCTTC[C/T]TCCCCTAGTGAGGGA | 237711 |
rs213190000 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29940018 | GAAAAATCCACTAGG[A/G]TGAACTGACAATTTC | 237711 |
rs213196426 | snp | A/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29831978 | ATCTCACCAGCCCCA[A/T]AATCTTTATTTTTAA | 237711 |
rs213200749 | in-del | -/G | | | intron-variant | Eml6 | Mm_Celera | 11:29851048 | GAGAAACCCTGTCTC[-/G]AAAAAAGAAAAAAAC | 237711 |
rs213202833 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29932239 | GACCAGACTGGCCTC[A/G]AACTCAGACACACAC | 237711 |
rs213217425 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29839752 | TTTCAAATAAAGAAC[A/G]GGGGAACAGATATCT | 237711 |
rs213248002 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29893996 | GTTCTGTAAAGTGTT[C/G]ATAGAAAGGAATGGG | 237711 |
rs213249854 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29984823 | AGAACTATCACATTC[A/G]GAATCCATTTAAACT | 237711 |
rs213256431 | snp | G/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29820956 | AGCCATGTTGTCTTC[G/T]AATTCTTCTTCTTAT | 237711 |
rs213287729 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29872062 | CACTGGGGCCATCAT[A/G]AGGATGTTGGGTGTT | 237711 |
rs213298522 | in-del | -/T | | | intron-variant | Eml6 | Mm_Celera | 11:29916275 | AAACAGCAGATGCAG[-/T]GTTACTATTTGGATG | 237711 |
rs213330915 | snp | G/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29747001 | AGTAGATAGGAATTG[G/T]AGGTCATTTGGTCAC | 237711 |
rs213332011 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29952712 | AACACAACTATATTA[C/T]AATGCACCCTCCACA | 237711 |
rs213339527 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29766930 | CGATTCTTCTTTCCA[C/T]TGGCCTGGCTGCTGA | 237711 |
rs213342771 | snp | C/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29852760 | CACTCCCTTGTCAGT[C/T]GTACTATTTCCCTAA | 237711 |
rs213348805 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29855163 | CCCTTAAAGAGGAAA[C/T]AAATAAATCCCTTAA | 237711 |
rs213354522 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29846944 | CAGAGGTGTGTAGCA[A/T]TGGGGGATGGGGAAC | 237711 |
rs213361515 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29747682 | ATAAACAGTCCGTTG[C/T]CCCACAGCCCATGCT | 237711 |
rs213368220 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29906085 | GGCTGCCAAGGGTAA[G/T]CAGCAAATATTGGTA | 237711 |
rs213368418 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29897065 | TAATCAGTTAAACAC[A/G]CAGGAGAAAGTTTAT | 237711 |
rs213371763 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29953289 | AAAACATTAACTAAA[C/T]GGGAGACTTTAAAAT | 237711 |
rs213372266 | snp | A/C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29850003 | CCCCCACCCCCCCCC[A/C/T]CCCCCGTCTAGGAAT | 237711 |
rs213374029 | in-del | -/T | | | intron-variant | Eml6 | Mm_Celera | 11:29929965 | TCACTAGTGTCCTAG[-/T]TAGGGTTTTACTGCT | 237711 |
rs213374309 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29903368 | AGTATTCAGCTTCAC[C/T]GAATGCCAGGACACA | 237711 |
rs213375101 | snp | G/T | | | upstream-variant-2KB | Eml6 | Mm_Celera | 11:30026132 | CCTTTGCCCGCCTGT[G/T]CCCTATGCATCTTGG | 237711 |
rs213379953 | in-del | -/TGTG | | | intron-variant | Eml6 | Mm_Celera | 11:29769420 | GGAGCATCCTCAGCT[-/TGTG]TGTGCATGGCTCACC | 237711 |
rs213432469 | snp | C/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29809856 | TTCTTACAAAGGAAA[C/G]GACCTCACAACTGAA | 237711 |
rs213487300 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29779420 | TAAAATAATAAAAAT[G/T]AATCAGAGAGGAAGA | 237711 |
rs213491812 | snp | A/C | | | intron-variant | Eml6 | Mm_Celera | 11:29981374 | TGTATCAGAAGATGG[A/C]CTAGCTGGCCATCAT | 237711 |
rs213495469 | in-del | -/T | | | intron-variant | Eml6 | Mm_Celera | 11:29935331 | TTTTCTTTTTCTTTC[-/T]TTTTCTTTTCTTTCT | 237711 |
rs213505560 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29909115 | CATCCCAACATAAAG[A/T]ACTGGCACCCTGCAA | 237711 |
rs213506999 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29885921 | AGATTAATTTAGATA[A/G]GGGCTATGCTTCAGG | 237711 |
rs213519916 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:30000365 | TGCTTGCTTCTTTTT[G/T]TTCTAGGGCTTTCAG | 237711 |
rs213521950 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29835325 | TACTCATTGTCCACC[C/T]GAGACTAGAGACCCG | 237711 |
rs213522986 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29912972 | CATAATGTGGGGTGC[C/T]GTGTGTGAGGGGAAA | 237711 |
rs213543051 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29779832 | GCAAGCACAGTACCA[C/T]TTATCCTTAGATCTG | 237711 |
rs213543465 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29941845 | ACAAATAAATCAGTT[G/T]CCTTCCTACACTCAA | 237711 |
rs213562964 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29946504 | ACTTCAACTTCAGAC[A/T]AGCAGGCTGAAAGTT | 237711 |
rs213573731 | snp | C/T | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29835785 | GACTCCCCAGCTATT[C/T]TGCCCTATCTGTTTG | 237711 |
rs213575693 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29897696 | CAGACCCCAGGAGGC[G/T]CAGACGGAGGATTTA | 237711 |
rs213581268 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:30005357 | TACACCTACCTCACA[C/T]GGACAATGGCAGGGT | 237711 |
rs213596198 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29841927 | TAAAATCACATCTCA[C/T]GATGATGATAGAGGA | 237711 |
rs213596402 | snp | A/T | | | intron-variant | Eml6 | Mm_Celera | 11:29784990 | GTTCAGACTCTACAT[A/T]TTTCATAGGCCTGAT | 237711 |
rs213600818 | in-del | -/A | | | intron-variant | Eml6 | Mm_Celera | 11:29793232 | ATTTTTTTTTTTTTT[-/A]AAATTTAGAAGCCCT | 237711 |
rs213601779 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:30008673 | CTTCAATCTCTTATA[G/T]CAGTGGTTCTCAGCC | 237711 |
rs213635948 | snp | A/T | | | intron-variant | Eml6 | GRCm38.p3 | 11:29846260 | GCCCTATTTAAAATT[A/T]TAAAAAAAAGGGGGG | 237711 |
rs213647673 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29933398 | CCTCTGTGTCAATGG[A/G]ATATCATGCTTGATA | 237711 |
rs213649974 | in-del | -/C | | | intron-variant | Eml6 | Mm_Celera | 11:29914869 | CCAATTATTAAAGAG[-/C]CACTGTTAAAAGTTC | 237711 |
rs213655468 | in-del | -/AAGCACACAAGCAGAGAGAAACAG | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29815508 | TGGAAACCCTGAATA[-/AAGCACACAAGCAGAGAGAAACAG]AAGCACACTGCAGTT | 237711 |
rs213660465 | snp | G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29785593 | TCTTCTAGAAGAGCA[G/T]CCAGTACTCTTAACC | 237711 |
rs213663153 | snp | A/G | | | intron-variant | Eml6 | GRCm38.p3 | 11:29931513 | AAGCTAGAAACTTTG[A/G]GGAACAATTGTAATT | 237711 |
rs213671135 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:30007756 | TCCTTAATTCCTCTT[C/T]GTCTGTTTCCTCAAG | 237711 |
rs213676511 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29863159 | GGTAAATAATATTTC[C/T]CTTTCTTTCTTTTCT | 237711 |
rs213695154 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29923610 | AGAAGTGGATGCTCA[C/T]AGTCATCTATTGGAT | 237711 |
rs213703556 | snp | A/G | | | intron-variant | Eml6 | Mm_Celera | 11:29792909 | ACTCCCTGTAACTAC[A/G]GCTTCAAGTACTCTG | 237711 |
rs213704342 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29995581 | TTTCTCTTAAAACTT[C/T]ATAGGAAGCTGGGCG | 237711 |
rs213715726 | in-del | -/C | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29810705 | TGCAAGGACTTACAT[-/C]AAAAAAATTCTTATC | 237711 |
rs213728134 | snp | C/G/T | | | intron-variant | Eml6 | Mm_Celera | 11:29923860 | GGAAGTGGGTGGGTA[C/G/T]GGGAGCAGGGCGGGG | 237711 |
rs213745104 | snp | C/G | | | intron-variant | Eml6 | Mm_Celera | 11:29863543 | TTCCTACTGACAGCG[C/G]TGAGCTGAGAGACAC | 237711 |
rs213748150 | snp | A/G | | | intron-variant | Eml6, LOC105243970 | Mm_Celera | 11:29811579 | GGGGCTCTTTTTTAG[A/G]GTTTCTCTGAGCTCC | 237711 |
rs213754081 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29782684 | GCAGGCATCACTTTA[C/T]AAAGCTCAACAGTCA | 237711 |
rs213754299 | snp | C/T | | | intron-variant | Eml6 | Mm_Celera | 11:29968738 | TTAAAGCTACTGTAG[C/T]CACATTTCAAATATA | 237711 |