SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6190059 | snp | A/G | 0.5 | 0 | intron-variant | Hdac4 | Mm_Celera | 1:92172252 | CATCCTACAGATGGC[A/G]TGAGATGAACCAAGA | 208727 |
rs6190698 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | Mm_Celera | 1:92172405 | TATTCCCCAGGCAGA[C/T]AGTGCCAAAATCAGC | 208727 |
rs6284237 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | Mm_Celera | 1:91955391 | CCCTGTGCCCACCTG[C/T]GGCCACAAGGAGAGA | 208727 |
rs6284354 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Hdac4 | Mm_Celera | 1:91955463 | TTGAACTAGGGTGGA[C/T]TGGACTGGCGTGCCC | 208727 |
rs6285286 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91955614 | TGAACTAGGAGGAAT[C/T]ACTGAAAGACAAAAG | 208727 |
rs6352576 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Hdac4 | Mm_Celera | 1:92044192 | GCTGGAGTCCCTCAC[C/T]AGCTCCAATCTGCTG | 208727 |
rs6353056 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | Mm_Celera | 1:92044269 | AACACAGGATTGAAT[C/T]CTCAGCANTAGGCTG | 208727 |
rs6353068 | snp | C/G | 0.5 | 0 | intron-variant | Hdac4 | Mm_Celera | 1:92044277 | ATTGAATNCTCAGCA[C/G]TAGGCTGCAGTGTAG | 208727 |
rs6353499 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Hdac4 | Mm_Celera | 1:92044321 | GCTCTCCCAGCAGCA[A/G]CAAAGCCCAGAGGTT | 208727 |
rs6353587 | snp | A/C | 0.5 | 0 | intron-variant | Hdac4 | Mm_Celera | 1:92044366 | CAAATTTTAAATCAT[A/C]ATCATTAAATTAAAC | 208727 |
rs6356589 | snp | A/G | 0.5 | 0 | intron-variant | Hdac4 | Mm_Celera | 1:92038322 | agagtaaactgactt[A/G]cacccagaggcatnt | 208727 |
rs6356608 | snp | A/G | 0.5 | 0 | intron-variant | Hdac4 | Mm_Celera | 1:92038336 | tncacccagaggcat[A/G]taggctagcacacat | 208727 |
rs6356671 | snp | A/G | 0.5 | 0 | intron-variant | Hdac4 | Mm_Celera | 1:92038374 | agcacacaagcgcgc[A/G]cncacacacacacac | 208727 |
rs6356673 | snp | A/G | 0.5 | 0 | intron-variant | Hdac4 | Mm_Celera | 1:92038376 | cacacaagcgcgcnc[A/G]cacacacacacacac | 208727 |
rs6358171 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91933058 | AAGCTTCTTCCTTCG[A/C]GGCTTCCCAGGGGGA | 208727 |
rs6358662 | snp | A/C | 0.207612 | 0.24638 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91933132 | CCCGTGTGTTGCGCG[A/C]TGTCCTGTGTTCCAT | 208727 |
rs6359127 | snp | C/T | 0.498615 | 0.0262793 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91933213 | GGGCGGCAGAAAGGC[C/T]TCCCGTTGCTGCTGC | 208727 |
rs6359582 | snp | A/G | 0.207612 | 0.24638 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91933286 | ACGCAGGAGTGATAC[A/G]GGTAAGTTTCTTGGC | 208727 |
rs6366413 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Hdac4 | Mm_Celera | 1:92044486 | ATACTATCCCCAGAC[C/T]CTGTATCTTCAGATC | 208727 |
rs6367471 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Hdac4 | Mm_Celera | 1:92044651 | GGCATGTAAGGGCTG[C/T]TTGATCCACAGAGGC | 208727 |
rs6367521 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Hdac4 | Mm_Celera | 1:92044678 | AGGCTCCAATCTGCA[G/T]CTCCAGCCATTGTTC | 208727 |
rs6370212 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Hdac4 | Mm_Celera | 1:92038574 | ATTTTATCCATACAT[A/G]CCGGACAAATGTCTC | 208727 |
rs6370722 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Hdac4 | Mm_Celera | 1:92038660 | AGAATTCCACGCTAT[C/T]AAGTGACTAGAAAGT | 208727 |
rs6370776 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hdac4 | Mm_Celera | 1:92038694 | CCCACTTTTTAGTCT[C/T]AAAAATGGATTTTAT | 208727 |
rs13474690 | snp | A/G | | | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91929568 | TCTGGCAAGCTGGCT[A/G]GGGGCATTTTCTTTT | 208727 |
rs13474691 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91929519 | TTTTCTCTCCCCACA[C/T]AGGGCCAGGTGCACC | 208727 |
rs13475981 | snp | C/T | 0.477291 | 0.104109 | intron-variant | Hdac4 | Mm_Celera | 1:92035888 | TGGAGGGGCTGAAAA[C/T]TCCTCCATAGGCTGT | 208727 |
rs30463752 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Hdac4 | GRCm38.p3 | 1:92060967 | TCCTGAGTTAAGGAT[A/G]TATGTGTTGTATGTG | 208727 |
rs30468291 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91933054 | CCACAAGCTTCTTCC[C/T]TCGAGGCTTCCCAGG | 208727 |
rs30472740 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92023377 | CCTCAGGTCACAGTA[C/G]TGAGTAAAGTAACTA | 208727 |
rs30494535 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:92033184 | ACGACAGGCCAATCA[C/T]CCCTGCCAGTGAACC | 208727 |
rs30496007 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Hdac4 | GRCm38.p3 | 1:91933830 | ACTCAGTGACTCCCC[A/G]CTTCTGCAGGTTAAT | 208727 |
rs30498501 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:91988011 | TTGTTTTTTTTTTTA[A/G]CTTCGAAAGGTCAAA | 208727 |
rs30505246 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | GRCm38.p3 | 1:92011423 | GCTAGAGAGATCCCC[A/T]TCCACTACAGAGCTG | 208727 |
rs30512724 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91984839 | CCAATACAAGCAGCA[C/T]ACCCAGGGCTGCAAG | 208727 |
rs30524049 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | Mm_Celera | 1:92101211 | TTGTTTGTTTGTTTT[A/T]AAAAAAAAAAAAAAA | 208727 |
rs30528203 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | Mm_Celera | 1:91936329 | AGAGCAAGGGCCCCC[A/G]TGAAGCACTGGTGAC | 208727 |
rs30550725 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91939333 | AATGGTTTCCCTTCC[C/T]CTGTTACATCCTGCT | 208727 |
rs30558969 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91984879 | AGCATGAGGTGCTGA[C/T]GTGTGGTTGCCTGGT | 208727 |
rs30565856 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92019338 | GCAAGCCAGTAAGCA[A/G]CACCCTTCCATGGCG | 208727 |
rs30565861 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Hdac4 | Mm_Celera | 1:91932721 | CAGGCTCACATTTCT[A/G]TTCTGTCCAGTTTTT | 208727 |
rs30566253 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91956546 | GCAACCCCTTTGGGG[C/T]TGCATATCAGAGTTC | 208727 |
rs30572404 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Hdac4 | GRCm38.p3 | 1:91977984 | ATGTGAACAGCTGAG[C/T]CTCATGATGCTCACA | 208727 |
rs30593351 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92019582 | CTCAGATTACTTTCT[C/T]TTTTTCATTCAGTCC | 208727 |
rs30611750 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Hdac4 | GRCm38.p3 | 1:92001065 | TTCCATGTAAATAAA[C/T]GGGCCACTTTAGTGG | 208727 |
rs30618645 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Hdac4 | GRCm38.p3 | 1:91990570 | AGAGTAAGCAGGAGA[C/G]AACTGCATGAAAAGG | 208727 |
rs30659397 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:92072780 | ACAGACAATAGAGTG[C/T]CTCATAGAAATGTTG | 208727 |
rs30660551 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Hdac4 | Mm_Celera | 1:92027309 | ATCTAGAAATATGGA[A/G]TAGTGGGGCGTGCTG | 208727 |
rs30660786 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91993963 | GGCAGCTGCGCTCTG[C/T]GCATGAGAAAGGTCA | 208727 |
rs30660946 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92149893 | TATGTCAACTGATCT[G/T]CACTCAATAACACCA | 208727 |
rs30702728 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:92027261 | AGGCCAGCCCTGAAG[C/T]TAGATTTCTGGGCCT | 208727 |
rs30704064 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92032427 | AAATGAAACAAGATG[A/G]AAAAGTTATCAGGCC | 208727 |
rs30711918 | snp | A/C | 0.375 | 0.216506 | missense | Hdac4 | GRCm38.p3 | 1:91975501 | CTGTCTCTCGAGTGG[A/C]CTCCGCTTCTTCCTC | 208727 |
rs30714536 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Hdac4, LOC105246664 | GRCm38.p3 | 1:92181466 | GAGTTAGAAAGCTTC[A/G]TTCACTGGGAGAAAT | 208727 |
rs30752356 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hdac4 | GRCm38.p3 | 1:92011560 | CCAGCTTCCCTTTCA[C/T]TCTTTGTTGTCATAG | 208727 |
rs30761657 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Hdac4 | Mm_Celera | 1:92026797 | CAATTCTGGCTAATG[A/C]CACAGCACCCCCTCT | 208727 |
rs30766209 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:92005402 | ATCTTTTGATAAACA[C/G]CCACTATTTCCCCTA | 208727 |
rs30796840 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:91935750 | TGGAACTGCTGATAA[C/T]TCCAGAGGGCAGAGC | 208727 |
rs30811262 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91967043 | GCAGGACAGTGGGCT[A/G]TAGAGGGCAAAACAA | 208727 |
rs30821156 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:92029160 | AGGCCTCAGATGCGA[A/C]TAGCATGACCAACAT | 208727 |
rs30836730 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Hdac4 | GRCm38.p3 | 1:92026223 | ACCTCCCTTCCAGCC[G/T]CTCAGGATGCATCTA | 208727 |
rs30853111 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91931490 | TACTAGCGGTGTTGC[A/G]GGGCAGAAGCCCCTG | 208727 |
rs30870176 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91958918 | TGCGCGCGCGCACAC[A/G]CACACACACACACAC | 208727 |
rs30884356 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Hdac4 | GRCm38.p3 | 1:92011323 | AGCACAGGCAAAGGC[C/T]TGACTGAACACTCTC | 208727 |
rs30895093 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92005774 | GCCAGATCGGCTGGC[C/T]GGAGAGTGATACATG | 208727 |
rs30896987 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92123799 | AGGACACCCTGCTGA[A/G]GTTCTATCACCTAGA | 208727 |
rs30944960 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Hdac4 | Mm_Celera | 1:92032628 | TCCCCCTATTTTGAG[C/T]TCACATATACGATCC | 208727 |
rs30955801 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92023721 | GATAACACAAGTAAC[C/G]ACCCCCCTCAAAAAT | 208727 |
rs30957942 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Hdac4 | Mm_Celera | 1:91997159 | AGAATGGACTGAAGG[A/G]ACTCTCAGACACATC | 208727 |
rs31009217 | snp | C/T | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:91999241 | TGCCCTACCTGTCTG[C/T]GAAGGGAGAGCCCTG | 208727 |
rs31033254 | snp | A/G | 0.455 | 0.143091 | intron-variant | Hdac4 | Mm_Celera | 1:92001308 | TCTACAGCACACCAC[A/G]AACAGCCCATGTTGG | 208727 |
rs31045861 | snp | C/G | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:91987704 | CATTGGGTAGACTCA[C/G]AGAGCCCTACTGCCT | 208727 |
rs31052514 | snp | A/G | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:92017306 | TCAGGAGCATGGAGT[A/G]GGTCATTGATGAAGA | 208727 |
rs31058838 | snp | A/T | 0.255 | 0.24995 | intron-variant | Hdac4 | GRCm38.p3 | 1:92129155 | ACAGACCCAAGACTT[A/T]CCCAGGCTCAAGGAA | 208727 |
rs31099961 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92002314 | GAGGAGGAAGCAGTA[C/T]GGAGCAGGCAGTATG | 208727 |
rs31137204 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Hdac4 | GRCm38.p3 | 1:92032205 | ATGAGCTAATCTCTC[C/T]TACCACACATAGTAG | 208727 |
rs31140504 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hdac4 | GRCm38.p3 | 1:92015170 | TTTATGGAAGACAAA[C/T]AGATGTACCCAGAGA | 208727 |
rs31148914 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91958916 | CATGCGCGCGCGCAC[A/G]CACACACACACACAC | 208727 |
rs31153584 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92035849 | CGTCAGAACAATAAT[G/T]CCTGTATGCTCAGGA | 208727 |
rs31163257 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91984143 | AGCTGTAGGGAAACC[A/T]ATCAGTGGGAGAGCA | 208727 |
rs31185137 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Hdac4 | Mm_Celera | 1:92023654 | GTTAAAAGAGCTGAG[A/G]AAATTTCAGTTAATT | 208727 |
rs31188852 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:91956491 | GGGTTGGCTACTTAC[A/T]GGCACGTCACAAAGG | 208727 |
rs31218975 | snp | C/T | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:91987508 | TACAAGGCAGGTATG[C/T]GGGGTGCTTGGCCTA | 208727 |
rs31247451 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:91944297 | AGCAGGGTTTCTCTT[A/G]TAATAGTGTCCACAG | 208727 |
rs31261304 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92027551 | ACAACGTTGACTATT[C/T]ACTATACCTGCTAGA | 208727 |
rs31265040 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:92048699 | TTTAAAAATAGATGC[G/T]TATTGCATGGGGTGG | 208727 |
rs31284498 | snp | A/G | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:91983604 | CTGAGTGTAGGGAGC[A/G]GTCCATGGTCACTGA | 208727 |
rs31286515 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92023362 | CCTAAACTTGCTGTT[C/T]CTCAGGTCACAGTAC | 208727 |
rs31318047 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hdac4 | Mm_Celera | 1:92020171 | AGCCATTTTTTTCAA[A/T]GAAAGCTGGTTCCTG | 208727 |
rs31327036 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92035103 | TGTGTGGACTACAGC[G/T]CTCCAGAGGGTACCT | 208727 |
rs31356893 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92092299 | GGAGTGTATGGTTTA[A/G]AGTAAACCCACTGAG | 208727 |
rs31372649 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:91950825 | CAGTGGCTTCTCTGC[A/G]GGTGAGCACAGCATA | 208727 |
rs31374183 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91931475 | CTGCCCGCCCTGTAA[C/T]ACTAGCGGTGTTGCA | 208727 |
rs31374412 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hdac4 | Mm_Celera | 1:91964604 | AAAAACCAAAAAAAA[A/C]CAAAAACGCTCTCAG | 208727 |
rs31374952 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92032400 | GCCTTGCCTTTTTAA[C/T]CTCTTATTACAAAAT | 208727 |
rs31380367 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91989735 | CAGCATGAACTTCAT[C/T]CCAGCTGGGAAGAGT | 208727 |
rs31380476 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91972236 | AAACTAAAGTGGCAC[C/T]GAGACACTACTTCCA | 208727 |
rs31403786 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91970426 | GGAGAAGAGGCTAGA[C/T]ACCCAATATGGTAGT | 208727 |
rs31421674 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91995778 | TAGAACTAACCTACT[G/T]CTCTGGACTGTAGAG | 208727 |
rs31424621 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:92011431 | GATCCCCTTCCACTA[C/G]AGAGCTGGGACTGAG | 208727 |
rs31429775 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Hdac4 | GRCm38.p3 | 1:91944030 | TGTGGCTGACTGCTG[C/T]CTCTGACCCGCCTCC | 208727 |
rs31455739 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:92022998 | CTTCCCCATCATGAA[C/T]AGGGCTTCAAGCAAC | 208727 |
rs31470248 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Hdac4 | GRCm38.p3 | 1:91991012 | GAGAGGAGCTTCCTC[C/T]GGTGAGAAGGGCTGT | 208727 |
rs31473214 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:91997530 | TTAGGTATTTTCCTC[A/G]TTTACATTTTCAATG | 208727 |
rs31476946 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:92024140 | GGCAGTCAGCCTAAC[A/G]TCTATGTGGGCACCA | 208727 |
rs31477106 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92007805 | GAAATCTTCACTAAC[A/C]CCACATCTGATAGAG | 208727 |
rs31481954 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91965023 | AAGCAGCGTTTTATG[A/G]GTAGGCAGCCACAGG | 208727 |
rs31487916 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91973501 | ACATACTGTGGGGGA[A/G]ATAGAATCTGGGTGG | 208727 |
rs31498630 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91985828 | TTCTTCTTGGGGTTG[A/G]AGCAGAGGTTAGGCT | 208727 |
rs31507232 | snp | C/G | 0.429688 | 0.173817 | intron-variant | Hdac4 | GRCm38.p3 | 1:92017237 | CAATCATTTTATAAT[C/G]ATCCATTCCAAGAAA | 208727 |
rs31511345 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Hdac4 | GRCm38.p3 | 1:91951557 | TGCCTTCTCCTCCAC[A/G]GGCCTCCTCTGGTTT | 208727 |
rs31533051 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Hdac4 | GRCm38.p3 | 1:92017379 | ATCCTGTTATAGTCA[A/C]AAAGACATGCAAACC | 208727 |
rs31553744 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91988543 | GGGCTCCTCAGCTGC[A/G]GAGCTGATTCAGAAC | 208727 |
rs31567612 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Hdac4 | GRCm38.p3 | 1:91950110 | ATACCAAGAGTACTG[A/G]TGACTACAATTGCTG | 208727 |
rs31605056 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91935358 | GCCAAAGCCACTGCA[C/G]CCCCCCTGAGTGACA | 208727 |
rs31605180 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:91939108 | ATAATGCGTGACTGC[C/T]CTAGTCCAGTGATGG | 208727 |
rs31622906 | snp | C/T | 0.387812 | 0.208586 | missense | Hdac4 | Mm_Celera | 1:91955290 | CAGTGGGGTACTCAC[C/T]TGAAGGCTGCCAAGT | 208727 |
rs31627110 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | GRCm38.p3 | 1:91989785 | GCCCCTGGCCCTCCA[C/T]GCAGGGTGCAGGCCT | 208727 |
rs31643414 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91962777 | TCTGTAGACTACTCT[C/T]TGGGCATCACAGGTC | 208727 |
rs31645526 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91965526 | AAACATGGGAGGCAG[A/G]ACAGGAACAGTAAAT | 208727 |
rs31652441 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | Mm_Celera | 1:91997206 | AAGACTTCTTACATG[C/T]TAAGCTAATGGGGTC | 208727 |
rs31658679 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91991159 | AAAGGCCCCACTATG[C/T]CTGTGGGCAGCAGAA | 208727 |
rs31667089 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hdac4 | GRCm38.p3 | 1:91955081 | TTACATCCTCAGTTT[C/T]CAGTGACTCATGAAT | 208727 |
rs31672264 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91962478 | AGCAGTGTCCTAGGC[A/G]GCCCAGCAGTGTCCA | 208727 |
rs31681024 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Hdac4 | GRCm38.p3 | 1:92029006 | GTGGTTAATACCAAT[C/T]CAGGGGTTCTAGATG | 208727 |
rs31688209 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91998241 | GGATAGGAGGATGCT[A/G]GTTTACTGACCAGGC | 208727 |
rs31692318 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Hdac4 | Mm_Celera | 1:91997183 | ACACATCTAAGAAGG[C/T]AGCCCTGAAGACTTC | 208727 |
rs31694367 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Hdac4 | GRCm38.p3 | 1:91967803 | AAGAGACCAGAAGAA[A/G]CTCTAGCTCTGTCTC | 208727 |
rs31699939 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92123785 | TAGGCTGGGAGTTAA[A/G]GACACCCTGCTGAGG | 208727 |
rs31710062 | snp | A/G | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:91983483 | TCAGACGCTGCCTAC[A/G]GGAACTGAGTCTTTT | 208727 |
rs31714444 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91990009 | CCACCTTCTCCACAA[G/T]TTTACAGAGCAGACA | 208727 |
rs31715409 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:91978941 | AGAGGCCTCTTGACA[C/T]CAGGACCGTGTTTTA | 208727 |
rs31722108 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92023207 | CCAATTAAAAAAGGG[A/G]AAAAAAAGTGGTAAA | 208727 |
rs31728638 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Hdac4 | GRCm38.p3 | 1:91987427 | AATAGGGAATGACAC[A/G]TGGAAGGCCCTTCCC | 208727 |
rs31747078 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91935342 | CGGCTAGAATTCCCT[A/G]GCCAAAGCCACTGCA | 208727 |
rs31749155 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Hdac4 | GRCm38.p3 | 1:92033088 | AATTTTCACAGGAGG[A/G]TACCATTAGGAATGC | 208727 |
rs31765465 | snp | C/T | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:91995577 | CCCCTTTATACCCTT[C/T]GTCCATAAGAGAGCT | 208727 |
rs31769063 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:92004824 | TAAGAAATGAACTAA[C/T]GAACACTTTGCACTG | 208727 |
rs31771459 | snp | C/T | 0.387812 | 0.208586 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91930104 | AGTCTATCACCAGTG[C/T]TGTGGAGACCACTGC | 208727 |
rs31775700 | snp | A/G | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:92027482 | ATTTCTGAGACCCTC[A/G]CTATTTAAAGCATGG | 208727 |
rs31780310 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:91950918 | AGGCCACCTTCATTA[C/T]CAGTACTGTTATGGG | 208727 |
rs31780346 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92068272 | ACTTAATAATAAACG[A/T]TAAAGGGGCTAATGA | 208727 |
rs31782597 | snp | C/T | 0.401235 | 0.199068 | synonymous-codon | Hdac4 | GRCm38.p3 | 1:91984568 | ATCCTGCTGACCTGC[C/T]GCACCCTGAAAGGCA | 208727 |
rs31782880 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91950613 | CCTTTTGTGCATTTA[C/T]GTGTGTATTTGTGAA | 208727 |
rs31795618 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91985449 | GTCCTTTTTTGCAGA[C/T]TGATTTCGCAGTCTG | 208727 |
rs31806553 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91988540 | ACAGGGCTCCTCAGC[A/T]GCAGAGCTGATTCAG | 208727 |
rs31819905 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Hdac4 | GRCm38.p3 | 1:92011385 | ACTCACATCGCACCT[C/T]AATGGCAGTCAGGGA | 208727 |
rs31835550 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:92011027 | GAGGGGTCAGATGCA[C/T]ACTCTAAACTATGCA | 208727 |
rs31837658 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:92154645 | AATTAGCCTCAGCAC[C/T]ATGGAACTGGAGTTC | 208727 |
rs31839821 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Hdac4 | GRCm38.p3 | 1:91963032 | GTGGCAAATCTGGGT[A/G]AGCCCTGGGAATGAG | 208727 |
rs31842251 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Hdac4 | GRCm38.p3 | 1:92004486 | CCAAGTGAGGCCACC[A/G]GCCACCAGAGCTGTG | 208727 |
rs31849060 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92176783 | TCTGATTTCTGTGAT[A/G]CTCGGGATAGATAGA | 208727 |
rs31864181 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Hdac4 | GRCm38.p3 | 1:92032076 | AAAGGGTAGGAGCAG[A/G]CAGAGCCCAAGGAAT | 208727 |
rs31867424 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:92051734 | ACATGTAGCACACAC[A/G]TGAGTATCTACCCAA | 208727 |
rs31878278 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:92138229 | ATGTAATCGCTACAT[A/T]AAATAGGACAAATTT | 208727 |
rs31881667 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91987069 | CCAGGCATGTTGCTC[A/G]GGGAAGTATGTAGTG | 208727 |
rs31885002 | snp | C/T | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:91975771 | TTGTATGATCCAGGG[C/T]CAGCAAGTACTATTT | 208727 |
rs31897092 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Hdac4 | GRCm38.p3 | 1:91983446 | TCAACCTGGAGATCA[A/G]CACCGACTGGGCTGC | 208727 |
rs31919731 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92005766 | GTCAGTTTGCCAGAT[C/T]GGCTGGCTGGAGAGT | 208727 |
rs31921329 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Hdac4 | Mm_Celera | 1:92007332 | CTGCATTAGGAAAAA[A/C]GATAAAAGGTGAAAA | 208727 |
rs31923664 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91943622 | ACACCTGCCCAGAGC[C/T]CATGTCTCTGAATTC | 208727 |
rs31924609 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Hdac4 | GRCm38.p3 | 1:91962237 | TTATATGGGTGAAGA[C/T]ATTGCTGAGGTGGGT | 208727 |
rs31935333 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Hdac4 | GRCm38.p3 | 1:92026318 | CGTGTCACTCATTTT[A/G]GATTATCCACTGGCC | 208727 |
rs31943555 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Hdac4 | GRCm38.p3 | 1:91940776 | TGAATGACACATCCC[C/T]GGGTTTCAAAGGCCT | 208727 |
rs31968215 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Hdac4 | GRCm38.p3 | 1:91988459 | TAGCCCTGGACACAG[C/T]AGGCCACTGAAGGGG | 208727 |
rs31977182 | snp | C/T | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:92001034 | TTCCCCAGGTTGTGT[C/T]GTGGGAACTGAGGTC | 208727 |
rs32026430 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:92023018 | CTTCAAGCAACATGC[C/T]CTGGACTACTTGGAA | 208727 |
rs32032097 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91987858 | GCACGGTTGATCCTT[G/T]CAGGGTGTGCATGTT | 208727 |
rs32040358 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:92015626 | ACCTGTGTGGCCCAG[G/T]CATTGAGCCACTCAG | 208727 |
rs32040925 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hdac4 | Mm_Celera | 1:92020143 | TAAGGGATTTGTATA[A/C]TCATCTAAACATAGC | 208727 |
rs32050753 | snp | A/G | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:91972918 | AGGGCCATTAGTACA[A/G]ACCATTTCCCAACAG | 208727 |
rs32056585 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92004662 | GCCATGTAGTCTTAA[G/T]AACTCACTGTTGGTG | 208727 |
rs32068017 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:91973224 | CCTTGGCTGGGAGAA[C/T]CATTCTGGCCAGCGT | 208727 |
rs32077647 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92019207 | TTGCAGACAAGCCTA[G/T]AGGACACTTTCTTAA | 208727 |
rs32079110 | snp | A/G | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92116262 | ATGACCATATCACCT[A/G]CAAAGATGTGTTCGG | 208727 |
rs32090990 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Hdac4 | GRCm38.p3 | 1:91949299 | TTGCAAAAGTCTGGG[C/T]AGGTAATCTTTTAGT | 208727 |
rs32099650 | snp | C/T | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Hdac4 | GRCm38.p3 | 1:92115561 | CTCCAGCTCCACTTG[C/T]AAGCCCCACTGACAG | 208727 |
rs32102822 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91994049 | GAGCTGCCACCCCAG[A/G]GAACCAACCAAGGAC | 208727 |
rs32104436 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92123836 | CTGCTTACCACGGAA[A/G]GAAAAGGAGCAACCT | 208727 |
rs32112720 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91997062 | GCATTCCACACATCG[A/G]GAGTTATGTGAACCT | 208727 |
rs32133665 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91951257 | GGGATGCTCTCACAT[G/T]AGAGCAGGTGCTCCT | 208727 |
rs32148360 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:92023280 | GACCAGTCACCTCAT[A/G]CCTCCACACCCTACT | 208727 |
rs32159227 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Hdac4 | Mm_Celera | 1:92020050 | AACAGAAAATCTAGA[C/T]ATAAAACCAGACCCC | 208727 |
rs32160783 | snp | A/C | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:92139610 | GGACAGTGATACCTG[A/C]ACTCACTTAGAAAAA | 208727 |
rs32174167 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91953055 | GCTCTGACTGAGCTC[C/T]GACAACTTCAAAGCT | 208727 |
rs32174406 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:91995059 | CCTCACACATTGCAA[A/G]TATTAATCAAGCCCT | 208727 |
rs32185182 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92014417 | AGGGTTAAAGGTGTG[C/T]ACCAACATGCCTAGA | 208727 |
rs32201929 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:91986016 | GTAATAAGAGGTGTG[C/T]TAACTACCAGCACTT | 208727 |
rs32202194 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hdac4 | GRCm38.p3 | 1:91993871 | AGGAGTCCAGACCAT[C/T]TAACGGTTGGGCGGA | 208727 |
rs32202418 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91934577 | TCTGCCCTGGGTCCC[A/C]ACGATGACTTGGCCA | 208727 |
rs32223123 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91988814 | GTGGACTGCGTCACT[C/T]ACCAGTCCCCTGAGG | 208727 |
rs32224325 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Hdac4 | GRCm38.p3 | 1:92006564 | AAGCAGGTTAGCTTG[A/G]TTAAACCTGCTAGGA | 208727 |
rs32230109 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91985442 | AACTGCTGTCCTTTT[C/T]TGCAGATTGATTTCG | 208727 |
rs32236511 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:92002712 | TCTGTCCCCTTCTGT[C/T]TGGTGCCACATACTC | 208727 |
rs32245590 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hdac4 | GRCm38.p3 | 1:92103827 | GCTCTGATGCCAGTG[C/T]CTGAGAGGCCTAAGA | 208727 |
rs32254254 | snp | C/G | 0.32 | 0.24 | intron-variant | Hdac4 | GRCm38.p3 | 1:92009818 | TTCTGTAAGAGAGCA[C/G]GCTGAGCAAGTCATG | 208727 |
rs32259968 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | Mm_Celera | 1:92032871 | ACAGTGATAATTTGG[C/T]TTAAATAAAAACTCA | 208727 |
rs32264405 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91965439 | GCCAGCTTCTTACTA[C/T]CCCTGCCATTCTCCT | 208727 |
rs32274718 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91940550 | TTCCTGGATTTAATG[C/T]TATTTATTGAGCAAT | 208727 |
rs32282010 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Hdac4 | GRCm38.p3 | 1:91975990 | TAAGCTCGAGAGAGG[C/T]CACAGATGTTGTGAG | 208727 |
rs32284231 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92023119 | TGCATCTGTGAGGGT[A/G]TTTCCAGAAACTCCC | 208727 |
rs32284374 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Hdac4 | GRCm38.p3 | 1:92015713 | ATACCATGGGCATAA[C/T]AAAAGAGGTGCTGGT | 208727 |
rs32286456 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92007658 | TCATTGGCACAGGGG[A/G]AAATTTCCTAAACAG | 208727 |
rs32297077 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92032390 | TACTCTCCTTGCCTT[G/T]CCTTTTTAACCTCTT | 208727 |
rs32297106 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92008281 | ACAGCGGCCTTATTT[A/G]TGATAGTCAGAAGCT | 208727 |
rs32305492 | snp | A/G | 0.498615 | 0.0262793 | synonymous-codon | Hdac4 | GRCm38.p3 | 1:91933712 | GGCGGTGACTGTCTC[A/G]GCTTCTTCCTTCTCA | 208727 |
rs32308140 | snp | A/G | 0.42 | 0.183303 | synonymous-codon | Hdac4 | GRCm38.p3 | 1:91987557 | CACCTCAGCTGGAGC[A/G]CTGGGCACAGTGGGT | 208727 |
rs32319879 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92032494 | GTAAGGAATTAAAGT[A/G]AGCCATCTCCGTTTA | 208727 |
rs32336986 | snp | C/T | 0.465374 | 0.126941 | intron-variant, upstream-variant-2KB | Hdac4 | GRCm38.p3 | 1:92030259 | GCTAGCCTTGAGGTA[C/T]GGGTCCCTCTTTCCC | 208727 |
rs32343882 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91996950 | ATGAGACATTCTGTG[A/G]TCTTGAGTACAGGAG | 208727 |
rs32348830 | snp | C/T | 0.337778 | 0.275914 | intron-variant | Hdac4 | GRCm38.p3 | 1:91969745 | TCAGAGCTTAGGACT[C/T]CTGAGTACACAGGGC | 208727 |
rs32351291 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Hdac4 | GRCm38.p3 | 1:92004775 | TGTATACAAAACTCA[C/T]TAAATACTAAATAAA | 208727 |
rs32370494 | snp | A/T | 0.32 | 0.24 | intron-variant | Hdac4 | GRCm38.p3 | 1:91981166 | CTGCTCCGAGGCCTA[A/T]GCTGGTCACTTCCTG | 208727 |
rs32371546 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | Mm_Celera | 1:92026833 | CAGCTGCCCTACCCC[C/T]CCTCAGGCTAGGGAG | 208727 |
rs32378737 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91967097 | GTCCCAGAAGACCTA[C/T]GATAGCCCTGCATCC | 208727 |
rs32392570 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91988646 | CTTCAGAGAGCGCAG[A/G]AGCTTGCCTCTATGA | 208727 |
rs32396133 | snp | A/G | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:91998970 | TAGCTTCATTGGGCT[A/G]AGTCCAGTTTTACAT | 208727 |
rs32423358 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Hdac4 | GRCm38.p3 | 1:92005821 | CACAGGCTGAATCTG[C/T]ACAAATTCTGCCTAT | 208727 |
rs32428029 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Hdac4 | GRCm38.p3 | 1:92167792 | AGCAGATAAGCCCAG[A/G]AGTGCCGTTAAGCAG | 208727 |
rs32429465 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:91950850 | AGCATATGGAGTGAT[C/T]CTATGTATGCTGTGT | 208727 |
rs32435146 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Hdac4 | GRCm38.p3 | 1:92135816 | GCTGCACACAAGCTA[C/T]GGCCAGAGCACTGTC | 208727 |
rs32437417 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Hdac4 | GRCm38.p3 | 1:92121821 | TTGACCTCAGATTCT[A/G]CACCTGAGCCTGGGT | 208727 |
rs32454083 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92035102 | CTGTGTGGACTACAG[C/G]TCTCCAGAGGGTACC | 208727 |
rs32472124 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Hdac4 | GRCm38.p3 | 1:91945405 | CCACTGAAGACTACT[A/G]TGCAGGCCAATGTCC | 208727 |
rs32476241 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91943653 | CAGTTCCTAGCTTCC[C/T]ACAGTAGGGTCAGGA | 208727 |
rs32477201 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:91966225 | GTTCTCCTCTCCAGC[A/G]CGGCTGTTAGGCCCC | 208727 |
rs32493341 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92019214 | CAAGCCTATAGGACA[C/T]TTTCTTAATTAATGA | 208727 |
rs32493382 | snp | C/T | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91933997 | TCCACGTCTGTGGGA[C/T]TCTGCCTTGCTGTGG | 208727 |
rs32495830 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hdac4 | GRCm38.p3 | 1:91948688 | CCTTTATAATCTGTG[C/T]ATGCAGGAGCACCAC | 208727 |
rs32499370 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:91935512 | CCCTCAAGCCATTCA[A/C]CAACAAAAGAAGTAA | 208727 |
rs32501251 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:92004295 | GGAACAGAAGAGCTA[C/T]TTGAAAAGTGAAACC | 208727 |
rs32512116 | snp | C/T | 0.498615 | 0.0262793 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91931601 | AAAAACCAAGCATGA[C/T]AGCAGCGCTCTTGCT | 208727 |
rs32525025 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:92023549 | TCAGACAGGAAGATA[A/G]CAGTAGGATCTAAGT | 208727 |
rs32533135 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:91943714 | GGCTGCCATCCCTAG[A/G]CTTCCTGGAGCATTG | 208727 |
rs32539073 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Hdac4 | Mm_Celera | 1:92027278 | AGATTTCTGGGCCTA[C/T]AGCATCTCTTCTAGG | 208727 |
rs32539317 | snp | C/G | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:92010591 | AGCAGGTTGCTAATT[C/G]CTTTTTCAAAATTGC | 208727 |
rs32543524 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Hdac4 | Mm_Celera | 1:92001136 | ACTCTAAGAAAAGCT[A/T]TTTTTTTCCCTGAGT | 208727 |
rs32550275 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92023722 | ATAACACAAGTAACG[A/C]CCCCCCTCAAAAATC | 208727 |
rs32555342 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91951288 | AGCTCCTGTGCTTTG[C/G]GAGCCCCAGAGCATC | 208727 |
rs32561338 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | GRCm38.p3 | 1:92009594 | GAGCTCAGCCTCAGG[C/T]CAACACTGCTGAAAC | 208727 |
rs32566527 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:92013922 | GATGGCTATCCTTTG[A/G]GCATGGGTACTTTTT | 208727 |
rs32570406 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91996868 | GGCACTGAGGCCATC[C/G]TAGGCGACCTTTAGC | 208727 |
rs32572787 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92150554 | TTTGGGGTTTTTTTT[G/T]GGGGGGGGTTGGTTT | 208727 |
rs32575218 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:91989683 | GAGTGTGAACCTTGA[C/T]TCCATGTGGCACAGG | 208727 |
rs32578511 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92028837 | TTCACCAGGGAAGGC[A/G]GGGCTCTGCTATCTA | 208727 |
rs32588470 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:91958903 | GCGCGTGTGCACGCA[C/T]GCGCGCGCGCACACA | 208727 |
rs32588727 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92163682 | CTGGTCTCATCCCAT[C/T]GGGATTTGTTGTTGT | 208727 |
rs32593476 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92001163 | GAGTAAAATTAATGA[C/T]TTCATTTTGATTTAG | 208727 |
rs32595935 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | GRCm38.p3 | 1:91990694 | TGTGCCTAGAAGGCC[A/G]CAGAGCCCTCTGTCC | 208727 |
rs32598092 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:91934870 | AAAAAAAAAAAAAAG[A/G]CTTGCTACAGGTAGT | 208727 |
rs32605810 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Hdac4 | GRCm38.p3 | 1:91988573 | CACTGTCTGTAAGTA[C/T]AGCCCTGCAAGACAG | 208727 |
rs32608041 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | GRCm38.p3 | 1:92035848 | GCGTCAGAACAATAA[C/T]GCCTGTATGCTCAGG | 208727 |
rs32616395 | snp | A/G | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:92026169 | TGGATGTTCTTCTCT[A/G]CTCCATAGCAGAATG | 208727 |
rs32620016 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91990932 | CCTTTTTCCTAGATG[A/G]TAAGATTCTAGGTGC | 208727 |
rs32623115 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:91966210 | AGTCACCCACGCCAG[G/T]TTCTCCTCTCCAGCA | 208727 |
rs32624823 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Hdac4 | GRCm38.p3 | 1:91935046 | ATCTGGCTTTTCTCA[C/T]ACATGCGGAAGGAGG | 208727 |
rs32627117 | snp | C/T | 0.42 | 0.183303 | intron-variant | Hdac4 | GRCm38.p3 | 1:91989930 | GTGTCCAGGTGGCTA[C/T]AGTGACCTGAGTAGC | 208727 |
rs32633746 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92008344 | TGGATACAGAAAATG[A/T]GGTTCATTTACACAT | 208727 |
rs32668095 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hdac4 | GRCm38.p3 | 1:92000969 | AGACATGCAGTGTGT[A/G]CAGCCACAGAGCCTA | 208727 |
rs32676836 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92112488 | TGTATGTATGTATGT[A/G]TGTGTGTGTGTGTGT | 208727 |
rs32692089 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Hdac4 | Mm_Celera | 1:91939155 | AAGGAACTCCACACA[C/T]AGGAAATACCACCCT | 208727 |
rs32692875 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Hdac4 | GRCm38.p3 | 1:92029237 | TAAAGACTGTTTGTC[A/G]CCAAAGCTATGATGT | 208727 |
rs32697697 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Hdac4 | GRCm38.p3 | 1:91990299 | TGCATAACCTAGGTA[C/T]AAGCAAGGAGTGGCT | 208727 |
rs32723760 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Hdac4 | Mm_Celera | 1:92005883 | TTGGAAAAGCCTTCA[A/G]TGCCTTTTGGGAATT | 208727 |
rs32728593 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91983252 | CTGGGAAGACTGGAT[A/G]GAGTGCTGGGGGAGA | 208727 |
rs32735741 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91958914 | CGCATGCGCGCGCGC[A/G]CACACACACACACAC | 208727 |
rs32737174 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91994031 | AAGGCACAACAGAGG[C/T]GTGAGCTGCCACCCC | 208727 |
rs32741451 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | GRCm38.p3 | 1:91969648 | GCACAGGGAAAGGAA[C/T]GAAGGCTCACCCGAG | 208727 |
rs32752198 | snp | A/G | 0.498615 | 0.0262793 | utr-variant-3-prime | Hdac4 | GRCm38.p3 | 1:91930084 | TGAGGAAAGAAACAC[A/G]ACCAAGTCTATCACC | 208727 |
rs32752805 | snp | A/C | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:92026173 | TGTTCTTCTCTGCTC[A/C]ATAGCAGAATGGATG | 208727 |
rs32769005 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Hdac4 | GRCm38.p3 | 1:92108831 | TGAGTGGCAGTCAAG[C/G]CATCATCTTGTCCAC | 208727 |
rs32782897 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | Mm_Celera | 1:91967649 | CTGGCTGAGTACCCG[C/T]AGAGGGGTCCCCTGT | 208727 |
rs32784477 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:91985655 | TAAAAGAACACAGGG[A/G]CTTGTACATATCAAC | 208727 |
rs32788878 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Hdac4 | GRCm38.p3 | 1:92004548 | CTATCTGACTCTGCC[A/T]GGACAGACCTCCTGT | 208727 |
rs32791250 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hdac4 | GRCm38.p3 | 1:91984239 | AGTTTTTTGCCACAG[C/T]TAAGGTAGCTATCAC | 208727 |
rs32791520 | snp | A/C | 0.32 | 0.24 | intron-variant | Hdac4 | GRCm38.p3 | 1:91998936 | GACCATCCCCTCTGC[A/C]CCTTTGCTGATGATT | 208727 |
rs32797476 | snp | A/C | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91936066 | CAACTGCCTGTACCC[A/C]TCAGGCCCTGCCCTC | 208727 |
rs32800926 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hdac4 | Mm_Celera | 1:92046875 | GCCAGTCTTTTACAT[A/G]TAATAGTAACAGTAA | 208727 |
rs32801814 | snp | A/G | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:91949369 | ACAGCAACCACAGAT[A/G]ATGAGGGAAGATGCA | 208727 |
rs32812846 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hdac4 | GRCm38.p3 | 1:92013268 | GCACATTCACCTGGA[A/T]GAATGCTGCCCACCT | 208727 |
rs33084359 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92169283 | GAATGCTCTCCACAC[C/T]AGGCATAGCACACCA | 208727 |
rs33084361 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92169270 | GTCTCTCTGGTCAGA[A/C]TGCTCTCCACACTAG | 208727 |
rs33084362 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92168625 | TAAGGCCCAGCATCT[C/T]CACACAGAGCAGGAA | 208727 |
rs33084363 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92168221 | GAGCAGTGTGAAGTC[A/G]AGGTAAGTTCTCATG | 208727 |
rs33085234 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92142874 | AGTTTTAAACACCTA[C/T]GGTTAAACAGACCCA | 208727 |
rs33085236 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92142725 | CTCACTTCCCAAGGT[C/T]ATCATGCCTTACAAA | 208727 |
rs33085237 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92142592 | AGAAGCGTGTGTGGG[C/T]GATGAATTCCAGTTC | 208727 |
rs33085238 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92142565 | AAGCACCCAGAGTTC[C/T]GCTGTCCACAGAGAA | 208727 |
rs33085239 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hdac4 | Mm_Celera | 1:92142373 | CAGGCCTTCTGGGGG[A/G]ACATCTCCATTAAAT | 208727 |
rs33085240 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92142126 | AAAATGCAGTACACA[C/T]ACCTAAAATGGTGCA | 208727 |
rs33085242 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92142081 | TCCAGGACCAGCAAC[A/G]AGAACTCAGAGAAGG | 208727 |
rs33085296 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92167558 | TAAGAGCAGCACATA[C/T]CTGCTTCAGTTCCAG | 208727 |
rs33085298 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92167310 | CAAAAGAAGTGTCCT[A/C]CCTCACTCTGAATAT | 208727 |
rs33085300 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92166954 | ACAGACAGGCCTTGA[A/G]AGAAGTGTCTCCTTG | 208727 |
rs33085302 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Hdac4 | Mm_Celera | 1:92166872 | TTTAAAAATGTTTTA[A/T]CAGTTTAAGATAAAC | 208727 |
rs33086204 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92166779 | CTGCTTCGCCACATA[C/T]TGGCTGTGTGGCTAG | 208727 |
rs33086206 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Hdac4 | Mm_Celera | 1:92166380 | ACACTGAGATAGAAA[G/T]GTCTGAGCAAGCGCT | 208727 |
rs33086208 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92166199 | CTGGGCTAAGAGGCT[A/G]ACCCCATATTCGAGA | 208727 |
rs33086210 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92166082 | GTAGACAGGCTCATC[C/T]CTACCAACACTCAAA | 208727 |
rs33086212 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92166056 | ATACACAGCAAGGGC[A/G]TAGTTCATGGGTAGA | 208727 |
rs33086394 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92141909 | GATGAAGCTCACTTC[G/T]TCTCTGTGTTAATCA | 208727 |
rs33086396 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hdac4 | Mm_Celera | 1:92141908 | TGATGAAGCTCACTT[C/T]GTCTCTGTGTTAATC | 208727 |
rs33086398 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92141726 | CAAATGCTATCTGAT[A/G]CAACTTTTAGAAATA | 208727 |
rs33086400 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92141701 | CTTTAGCCAACTTCA[C/T]AGTTCTTTACAAATG | 208727 |
rs33086402 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92141589 | CCCACCATCTAAAGG[A/G]AATACAGAGTCAGAG | 208727 |
rs33086955 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92133346 | AATAGATTCTTACAT[C/T]GTCTCAAGTGTAGAA | 208727 |
rs33086957 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92133285 | CAGCCCACAGGCCAA[C/T]TACAATCTATGGCTT | 208727 |
rs33086959 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Hdac4 | Mm_Celera | 1:92133227 | ACTACAGAGATAATG[C/G]CTTCACCAACTCTTT | 208727 |
rs33086960 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92133040 | GAAGAGGAGAGATAC[A/G]CAACCTCTCAGTTAA | 208727 |
rs33086962 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92132484 | TCCCAATTTACACCG[C/T]TTAAAATACCTCAAC | 208727 |
rs33086975 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92084968 | GAATCAGGACAAGAG[A/C]ACCATCAGTAGCATA | 208727 |
rs33086977 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92083785 | TTAGGACTTTTGTTC[A/G]GAGCAGGAAAGGATT | 208727 |
rs33086979 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92083524 | CTGCCACCGTTGCAC[A/G]TGGTCTCTTCAGAGC | 208727 |
rs33086981 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92083516 | TGACGCATCTGCCAC[C/T]GTTGCACATGGTCTC | 208727 |
rs33086983 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92083157 | GGAAACCAAATTCAG[A/G]AAATTCTATAATACC | 208727 |
rs33087034 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92165980 | GTCCTCCTTAACCAC[A/G]TGGAACCATCTGGGC | 208727 |
rs33087036 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92165940 | GTCAGACCTAGAACA[C/G]GTCGGATAGTGCTGG | 208727 |
rs33087038 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92165787 | CCTGTAGGGTCAGCA[C/G]TGCTCCTCACAAGCA | 208727 |
rs33087040 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92165505 | TGGGTCACCTCACAG[A/G]AACAGAATAAACCGT | 208727 |
rs33087042 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92164657 | TCCCCAAGTAGTTTC[A/G]TCTCTGTGCAGAAGA | 208727 |
rs33087095 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92121161 | AGCAGCAAGAGCACA[A/G]AGGGAGAACCTTGAC | 208727 |
rs33087097 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92119752 | CACCTGAAACACTAC[A/G]ACACCTCTGCAGCCT | 208727 |
rs33087099 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92119600 | CGGGGTTGTCAGCAA[A/G]GTCAGCCAGGAGTCA | 208727 |
rs33087101 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92119586 | GTAATCAGAGTCATC[A/G]GGGTTGTCAGCAAGG | 208727 |
rs33087103 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92119489 | CCAGGTAACAGCCAG[A/G]AATCCAGGACCTCGG | 208727 |
rs33087164 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-5-prime | Hdac4 | Mm_Celera | 1:92141549 | CTTGGTCATCAAGGG[C/T]TGACATGACTGGACA | 208727 |
rs33087166 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92140789 | ATCAAAGTTGGGCCT[C/T]CAGCTCTTTCCAGGA | 208727 |
rs33087168 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92140527 | GAATTATGCATCATG[C/T]TGTTAACTGGCTATG | 208727 |
rs33087170 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92140359 | TGAACATGTGGCCAT[G/T]GCACTTGACTAGATC | 208727 |
rs33087172 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92140331 | AACTGCCACTAACCA[A/G]AAGAGAGATGCATGA | 208727 |
rs33087705 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92106401 | GATCCAGCAGATGAG[A/G]AAGAAGCAGGTGAGA | 208727 |
rs33087707 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:92106398 | GGGGATCCAGCAGAT[A/G]AGGAAGAAGCAGGTG | 208727 |
rs33087709 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92106003 | TCTGACACCTCTTGT[G/T]ACCACACACTCAGCA | 208727 |
rs33087711 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92105622 | AATGGCACTGACACT[C/G]ATAAAAACTTTAATG | 208727 |
rs33087713 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hdac4 | Mm_Celera | 1:92105437 | CATCACTTGACAAAG[A/G]CTAAGTGTACTATGG | 208727 |
rs33087775 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92082386 | GGTGTGGTAGCTGCA[C/T]CTGCCAACCCCCAAG | 208727 |
rs33087777 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92082307 | TGATTTCGGAGTTCA[C/T]TAATTCATCATTCAT | 208727 |
rs33087779 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:92082290 | AGCCCAGTTCAGGTT[C/T]TTGATTTCGGAGTTC | 208727 |
rs33087781 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92082239 | GAGCTCGCCATAAGC[C/T]GAGTGTGATGACTAG | 208727 |
rs33087783 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | GRCm38.p3 | 1:92082231 | GGAAGTACGAGCTCG[C/T]CATAAGCCGAGTGTG | 208727 |
rs33087794 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92164644 | TCTGTGTAACTGGTC[C/T]CCAAGTAGTTTCGTC | 208727 |
rs33087796 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92163758 | GAACTAACAAGAACA[C/T]GCATTTTATAAAAGT | 208727 |
rs33087797 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92163463 | AAGTCCCCAAAGGCC[G/T]CCTGTCAATTACACA | 208727 |
rs33087799 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92163420 | TGCAAGCAGTAACTG[C/T]GAAGAGGTACAAGCC | 208727 |
rs33087801 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92163253 | GGAGTCACTGGCCCA[C/T]TCCCTAGGAGCAGTA | 208727 |
rs33087803 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92163224 | ACCACAGGCTTCAGT[C/T]AGGAGTACAGTGAGG | 208727 |
rs33087804 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92132401 | TGGACTTTACACCCT[A/C]GGAAGCAACAGAGGG | 208727 |
rs33087806 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92132352 | CAAGCCACATGCAAA[G/T]GATGAGAAGCTCAGC | 208727 |
rs33087808 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92132236 | CACCAGGATTGTCAA[A/G]GCAGTCAGAGCTCTG | 208727 |
rs33087810 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92132193 | AAATTTAAACTGTTA[A/C]AGATATAAGTGTCTG | 208727 |
rs33087812 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92132180 | CTGGTCAAGGATAAA[A/T]TTTAAACTGTTACAG | 208727 |
rs33087965 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92118884 | AAATAGAGCTGCATT[C/T]AATTACCTCTTTAGT | 208727 |
rs33087967 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92118828 | CTGAGTGGAACTGGA[C/G]GTACAGGTACAAGCA | 208727 |
rs33087968 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92118529 | AATGAAACATAGACA[C/T]GTGGATCGAGCCATG | 208727 |
rs33087969 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92118221 | GTAAAGTCCCAGTGG[A/G]CATACTGCCATATTC | 208727 |
rs33087970 | snp | G/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92118020 | AGCACAGTATGCCTA[G/T]AGGAACCACCTACCA | 208727 |
rs33087971 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92117967 | GGAAGAGAGGCTCTG[C/G]ATTTATCCAGACAGC | 208727 |
rs33087973 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92117894 | TCCCTCCTATGACGA[A/C]CTCTGGAAAAGCCTG | 208727 |
rs33088044 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92139853 | CCCTAACCTCCTACT[C/T]TCTACTATCACTGAG | 208727 |
rs33088046 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92139725 | TCCTTGATCCCTGGC[C/T]GAATGCCTCAGCTCC | 208727 |
rs33088049 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92139552 | CAGACTGATAGTAAC[G/T]GCATGGAGGTAGACA | 208727 |
rs33088051 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92139169 | GCATTCTCATGCCAG[G/T]ACATGCCAACCGGTC | 208727 |
rs33088053 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92139096 | CTCCCCAGGACAGCT[C/T]CAGCAAGTACCCAGA | 208727 |
rs33088475 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92105038 | AAATCAGTCACTGGT[A/G]TATTCTTTTCCCTGT | 208727 |
rs33088476 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92104895 | CAAACTGATCAAGGC[A/G]AGGCCATGCTGCAAG | 208727 |
rs33088477 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92104721 | CTATCCTAGCTTAAA[A/T]CGTTCCCAAGACTTC | 208727 |
rs33088478 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92104705 | ATCCATCACTAAATT[A/G]CTATCCTAGCTTAAA | 208727 |
rs33088480 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92104325 | AGCCTGTCCAGATGC[C/G]ACCACAATCACTATG | 208727 |
rs33088481 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92104112 | ACACTTTATGCCAAT[A/G]AGGGCTGGCCTATGT | 208727 |
rs33088482 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92103965 | CTAATTCCTTGACAT[C/T]CATTATTTCACTATT | 208727 |
rs33088485 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:92082155 | TCCCTATGGGTTTAA[C/G]GCACAGGATGAAACA | 208727 |
rs33088486 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92082120 | GAGCTGTCCTCACAT[A/G]AGCAGGCTACTGTCA | 208727 |
rs33088488 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92081523 | TCCCCATTAACAGAG[A/T]ATAGAATAGAATTGT | 208727 |
rs33088489 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92081421 | GGCTACCCTGGGGCT[C/T]TTGGGCCTGGCTGGG | 208727 |
rs33088491 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92081185 | CACTCTAGGTTTGTG[C/T]TGACAAGCCCCTGCC | 208727 |
rs33088492 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92081127 | TACCAAATGAGGGAA[C/T]CAGAACCTCCTCTTT | 208727 |
rs33088595 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hdac4 | Mm_Celera | 1:92163204 | GCTGGGAGAAGACAA[C/T]GCAGACCACAGGCTT | 208727 |
rs33088596 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92163144 | GACACTCAGGATGCC[A/G]GACAACTACAGGTCA | 208727 |
rs33088597 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92162880 | CTTCTGGGTTAGCTG[A/C]CCTCCCAATTCATGG | 208727 |
rs33088599 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92162704 | ATTAGAGCTCAAATG[C/T]TCCCACCTGCCCATG | 208727 |
rs33088601 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92161974 | AATGGTATGCAGACA[A/G]CAGAGAGCCCCCATG | 208727 |
rs33088602 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92161606 | GATAGCACTCATCTT[A/C]GGGAACGTATACCAG | 208727 |
rs33088624 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92132044 | CAGAACAGGGGCCCT[A/G]AAGAGTAGTCAAACA | 208727 |
rs33088626 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92131688 | CTAAGGTCTTTAACA[C/T]ACCCTGGCCCCACAG | 208727 |
rs33088628 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92131465 | CTCAGCATGTTACAT[C/T]AAATGCATGGATTAC | 208727 |
rs33088630 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92131409 | CAAATGCATATCTAA[A/C]TATTTACAACCAAGT | 208727 |
rs33088632 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92131393 | ACACAGCGAGTTATA[G/T]CAAATGCATATCTAA | 208727 |
rs33088925 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92138646 | AATTATAAAAGGTCT[A/G]AAAGTAGAACACGTT | 208727 |
rs33088927 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92138624 | AAATGTAACAGTGAC[A/T]TGTGACAATTATAAA | 208727 |
rs33088929 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92138567 | ATGTGTATAAACCTC[A/G]CTTTGAAGGTATTCA | 208727 |
rs33088932 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Hdac4 | Mm_Celera | 1:92137874 | TTTAGTCACCTCTGT[A/C]AGGTACAGTGTGATT | 208727 |
rs33089194 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92131385 | TTCAGTATACACAGC[A/G]AGTTATATCAAATGC | 208727 |
rs33089196 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92131235 | GCATGGTCAACTACA[C/T]ACAACCATGTGACAT | 208727 |
rs33089198 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92131132 | TTGCAGCAGCAGCAG[C/T]CTCCTCCCAGGATGG | 208727 |
rs33089200 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hdac4 | Mm_Celera | 1:92131128 | GCCTTTGCAGCAGCA[A/G]CAGCCTCCTCCCAGG | 208727 |
rs33089202 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92130511 | GACTTTGAGCAGCAA[A/T]AGTCCCTGCCTCTCT | 208727 |
rs33089285 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92117810 | TATGTGGTAAATGAG[C/T]GCAATAAAGTGTCGA | 208727 |
rs33089287 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92117677 | AGGGTATGATACATA[C/T]TCACCACACAGCACA | 208727 |
rs33089289 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:92117051 | AAAAAAAGAGCTGTA[A/T]AAAGTAAAAATAATT | 208727 |
rs33089291 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92116292 | GCAGGCCACAAAAGA[A/G]TGTCACAGGAGACAG | 208727 |
rs33089293 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92116129 | CAGCTCCTCTCAGCA[C/T]CCAGGTTATTCCAGC | 208727 |
rs33089384 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92081114 | TCCAGTTCTGAACTA[C/G]CAAATGAGGGAACCA | 208727 |
rs33089386 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92081059 | GCCCAAGTGAAGGGT[A/G]AGGAGAGTCATCAAG | 208727 |
rs33089388 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92080975 | GCCAGCCAACCAAGA[A/G]CTAGGGTGATTAGGA | 208727 |
rs33089390 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92080757 | GAATTCCATGCATAA[A/C]TAACTTTCTTTAACT | 208727 |
rs33089392 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92080534 | GGAAGAGGCCCAGGG[C/T]GGTGCTGTGCCTGGG | 208727 |
rs33089404 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92161549 | AAGTAAATGTCTTAT[A/T]TCCCATTCACCAAAA | 208727 |
rs33089406 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92161404 | AGAAGACAGAGGCAT[A/G]GTATCACCTGACTTG | 208727 |
rs33089408 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92161316 | GAGGAATCACATACT[A/G]AGAGGAAAGGTACAT | 208727 |
rs33089410 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92160964 | TCTCACTGCCACCTG[A/C]TAACTAAAATGGCAT | 208727 |
rs33089412 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92160922 | GAGAATGATTTAGAC[A/G]TAACAAGAACAACAT | 208727 |
rs33089544 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92137626 | AGACAAGGGTCCAAG[A/G]AGGGCACAGTGAAAA | 208727 |
rs33089546 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92137527 | TTGAGGAAGGCCAGG[C/T]AATATACATAGCCTG | 208727 |
rs33089548 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92137406 | CAGTGCAGACTGGAC[A/C]CAGGCCAGACTTGGG | 208727 |
rs33089550 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92137203 | TCCTTCCAAATATGA[A/G]GACAAAATAACAGCA | 208727 |
rs33089552 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92136715 | TAGAACTAGCACATG[C/T]TTTCTGCTCTACAAT | 208727 |
rs33089855 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | GRCm38.p3 | 1:92073854 | GAAGTCTATGCTCCC[A/G/T]ATACACCACCCCTTC | 208727 |
rs33089857 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92073138 | CTCTCTCTCTCTCAG[A/G]CTGACTGACTCACTC | 208727 |
rs33089860 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92072456 | AGGGCTCCCAGGTAA[C/T]TCTGCAGAACCTTCA | 208727 |
rs33089862 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92072166 | TGACTCCCAGGAACT[A/G]TCTCACAGGCTACCA | 208727 |
rs33089934 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92103804 | GTGCTGCTTGTTCTC[C/T]ATTCTAGGCTCTGAT | 208727 |
rs33089936 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92103743 | TCCCTTGAAGATAAA[C/T]CACTGAACTAAGGCC | 208727 |
rs33089938 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92103700 | TGTTAAGGACTACAC[A/G]TTCATCTTATTATCA | 208727 |
rs33089940 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92103541 | AGTTGGTCTCCCTTT[C/T]CTTAGATGCTGACAG | 208727 |
rs33089942 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92103406 | AAAAGTGGAATTTTC[C/T]CCAACACCAAAACGT | 208727 |
rs33089954 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92130045 | ACAGCAGTTACAAGT[C/T]GTTTTCCAGGAGTCT | 208727 |
rs33089956 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92129826 | AGACCTCACTCAACA[C/G]TACACTTGTAACTCT | 208727 |
rs33089958 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hdac4 | Mm_Celera | 1:92129166 | ACTTTCCCAGGCTCA[A/G]GGAACCACTGAGACC | 208727 |
rs33089959 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92129116 | CCACAGAGAACATTC[C/T]GCTCTCATTCCTAAG | 208727 |
rs33089960 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92128753 | ACACCCAAGTATAAA[A/G]GAAAGAGTTAAGTGC | 208727 |
rs33089961 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92128487 | ACAGTCGTACCTACC[C/T]GAGGTACCTAGGGCT | 208727 |
rs33089962 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92127366 | CCACTGGGGACTACA[A/G]CAAGCTCAGAGAGCA | 208727 |
rs33090185 | snp | C/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92115678 | AAGACTATCCCAGAA[C/G]AAGGCTGAGGGAAGT | 208727 |
rs33090188 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92115538 | CTACAGGAGCTGGAA[A/G]TCACAAGCTCCAGCT | 208727 |
rs33090189 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92115449 | CTTCAACAGTCTAGG[A/G]CAGTGGTCACAGGCT | 208727 |
rs33090190 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92115332 | GGGGGAAGTTGATGA[C/T]TGTTGTGCCAAAACC | 208727 |
rs33090191 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Hdac4 | Mm_Celera | 1:92114470 | ACCGTAACAGAGAAC[A/G]GCCTATCTGTCTCTT | 208727 |
rs33090193 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Hdac4 | Mm_Celera | 1:92114293 | GGCCTCGCTCCCATG[C/T]AGCCATCAGCCTAGA | 208727 |
rs33090214 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | GRCm38.p3 | 1:92080290 | AATCTGTAACTGTTC[C/T]GAGAAAAGCCCTGCA | 208727 |
rs33090216 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hdac4 | Mm_Celera | 1:92080196 | CAGTCCCAACCAAGG[A/G]ACAAACCCATCCAGT | 208727 |
rs33090218 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92080147 | GAACTGCACGTCACA[C/T]CCTACACAGGCCTAC | 208727 |
rs33090220 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92080077 | CATCTACCATGTCCA[C/T]GTGCCTAGAATCATG | 208727 |
rs33090222 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92079877 | CAGAGCAGTAGTACC[A/G]AAGGCCACAGGTAGG | 208727 |
rs33090314 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92160866 | TCCTGCCAGTGACTC[A/G]TGGCCAGTGTACCTG | 208727 |
rs33090315 | snp | A/C | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92158057 | CACATTTATAGTTTA[A/C]TTTCATAATAGACTC | 208727 |
rs33090317 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92157802 | GAATGCTAACCGATG[C/T]TTTGATTAAATGCTT | 208727 |
rs33090319 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92157757 | AAGGCAGACCCAAGT[C/T]AAAATGGTCAAAAAG | 208727 |
rs33090321 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92145178 | TAAAATCATAACGCA[A/G]GCCTCACCCAGCACC | 208727 |
rs33090323 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92145049 | CCAAGCCCTTTCCTC[A/G]GGCTGCTCACAGTAC | 208727 |
rs33090374 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92136678 | TCCGTCTCATCCCAC[A/G]AATATATCTAAGAGT | 208727 |
rs33090376 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92136659 | AAGACCATGGCATGA[C/T]GTGTCCGTCTCATCC | 208727 |
rs33090378 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92136534 | GAACCCATCCAGGAG[A/T]CCCACCTTTCCCTAG | 208727 |
rs33090380 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92136475 | TAATGGCTGAAAGCA[A/G]GCCTTTTCTTGGATT | 208727 |
rs33090382 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92136421 | TTAGTAGACCACAGT[A/G]CATAGCCAGGTCTGA | 208727 |
rs33090684 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92102946 | GGGCCATGCTACCTA[A/T]TCGAAGTCACAATCT | 208727 |
rs33090686 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92102429 | ACAACTTGCAAAAGA[A/C]GATATATAAGCAATC | 208727 |
rs33090688 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92101949 | AGTGGTTGGCTTGAA[A/G]ACCCCAGAGGCAGCA | 208727 |
rs33090690 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92100285 | TTTCATCTGGTTACT[C/T]GACGTCCCCAGTTGG | 208727 |
rs33090692 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:92100136 | CAGCCTGCTGCCAGG[A/G]CCTAGAGTACAAAAA | 208727 |
rs33090774 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92072124 | CAACCATTCTGACAG[C/T]CAATAACAATTAGGT | 208727 |
rs33090776 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92071977 | AACAGTTCCAAAGGA[C/T]CCAATGCCTTCTTCT | 208727 |
rs33090778 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92071663 | TCAAATGAATTCAAG[C/T]TCCAAGTCTCTACTC | 208727 |
rs33090780 | snp | G/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92071560 | TTTCAAAAGCAAAAT[G/T]GACAGGTTGGGGAAT | 208727 |
rs33091054 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92079801 | AACATTGTCATCCTG[C/T]TTGACACTTCTGGTC | 208727 |
rs33091056 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92079723 | AGTCCAGGAAGGCTG[C/T]AGCAGTGAAACAAGA | 208727 |
rs33091058 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92079618 | AGGAATAACCCAGGC[G/T]CTGGGGTGCATGTTC | 208727 |
rs33091060 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92079602 | AGAGGCAGCAGCAAA[C/G]AGGAATAACCCAGGC | 208727 |
rs33091062 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:92079432 | CAGAGGTGAAACAAG[A/G]GTCTCTTGGCCTCTC | 208727 |
rs33091154 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92127332 | TGCCACCGCAGTGCA[C/T]TCAGCTCCAAGGGCA | 208727 |
rs33091156 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92126991 | TAGGTGAAGGAAACA[C/T]AAGCTTGGGGCATCG | 208727 |
rs33091158 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92125532 | AAAACTCAGAGACAA[A/G]AACATAGACACTTAA | 208727 |
rs33091160 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92125439 | TCTGGTTCCACCCAG[G/T]GTGCACCATGAGGAG | 208727 |
rs33091162 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Hdac4 | GRCm38.p3 | 1:92125392 | GTACAGGGGAAGGAA[C/T]ATCTAGCCAGAAGCT | 208727 |
rs33091214 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92144701 | CTGATGATCAGTGTC[A/G]TGTCAGATGAGTGAG | 208727 |
rs33091216 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92144605 | TTCCTACCTAAGGCC[A/G]TCAGCTAAGGCGGCA | 208727 |
rs33091218 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92143878 | GCTGGCTAGCCCTAA[A/C]TGCCTACATACCTGT | 208727 |
rs33091219 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92143642 | TCTGAGGTATCTCAT[A/G]TCCTTTTCCAGAGAA | 208727 |
rs33091221 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92143529 | GGGCAGGAGGCAGCA[C/T]GAAGCACAGGAAGCA | 208727 |
rs33091254 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92136320 | AGGGACAAAGCAAGC[A/G]TTACACACTGGCATC | 208727 |
rs33091256 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92136294 | AGACAGGTGACCTCA[C/T]GCAACCATAAAGGGA | 208727 |
rs33091258 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92136035 | ATTTAAGCTAGGAAA[A/C]GCGAAGGGAGGCGCC | 208727 |
rs33091260 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92135935 | GGCTAGTCAATCCAG[C/T]GAAACATCCTCACAC | 208727 |
rs33091263 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92135732 | AATGCTGAAGAGTGC[A/G]TGTAGGGCAGACAGA | 208727 |
rs33091284 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-5-prime | Hdac4 | Mm_Celera | 1:92113965 | ACTAGAGAATAGGCA[A/G]GACAGAAAGGGGCCT | 208727 |
rs33091286 | snp | C/T | 0.336735 | 0.234472 | intron-variant, utr-variant-5-prime | Hdac4 | Mm_Celera | 1:92113252 | GGATCTCTGTTCAAT[C/T]TGAGAAGCCCCTCCA | 208727 |
rs33091287 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92112933 | CCTGCCAGCTCTCTT[C/T]CCTATACAGGGCTGT | 208727 |
rs33091289 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92112902 | CCGGAACAAGACCCC[C/T]GAGCACTGGGAGCTG | 208727 |
rs33091291 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92112773 | CTTTCTGCCCAGGTG[A/G]TGAACAGTTCACATT | 208727 |
rs33091293 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92112184 | GTGTACCCAGATATG[C/T]ATCACAGCTTGTGTC | 208727 |
rs33091434 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Hdac4 | Mm_Celera | 1:92099234 | ATCTATTTTCATTGC[G/T]GAAGGACATTTCTTT | 208727 |
rs33091436 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hdac4 | Mm_Celera | 1:92098776 | AAGACTCACTCCAAC[A/G]AAGACAGAACTTCCA | 208727 |
rs33091438 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hdac4 | Mm_Celera | 1:92097573 | AAATCTGCTCAGAAA[A/C]TATACAAGTTTAGAA | 208727 |
rs33091440 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Hdac4 | Mm_Celera | 1:92097374 | CTGCACGGCCTGCAG[A/C]TGAACTATCCCATTG | 208727 |
rs33091442 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Hdac4 | Mm_Celera | 1:92096717 | TCTAAGAATCCAAGT[C/G]AATGGACATCGTTGC | 208727 |
rs33091824 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92079337 | TCATCAGCTCCAGTC[C/T]TGCCCTGGTATCAAG | 208727 |
rs33091826 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92079311 | CAAGTAATAGGACTG[A/G]GAAACCCCTATCATC | 208727 |
rs33091828 | snp | C/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92078227 | CAACTTTTTAGAAAC[C/G]CACATAAAACTCTTC | 208727 |
rs33091830 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92077863 | GCAGGTCCCTGGGCA[C/T]GGCTTGAAGGGTATA | 208727 |
rs33091832 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92077834 | CTACTTCCTTGTGGT[A/T]GAGCTGCCCTCTGGC | 208727 |
rs33091844 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92125068 | AGAACTGTGTCAAAG[C/G]TGGTAGGGCAGAGTG | 208727 |
rs33091846 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92124537 | ACGCTCAGTGAAGGA[C/T]TTGTGTTGGGAATGA | 208727 |
rs33091848 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92124414 | GAACCTGGCATGTCA[A/G]CCATGATACCATTAT | 208727 |
rs33091850 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92124339 | AAAATGGGTAAACTC[A/G]GGGTTCAAGTACTTG | 208727 |
rs33091852 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92124027 | CTTTCCCTCAGTCAA[C/T]TCCATATGTCCTACA | 208727 |
rs33092035 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92135688 | AGGAGGCTTTATTCA[A/G]CAACAGTAAAGATGA | 208727 |
rs33092037 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Hdac4 | Mm_Celera | 1:92135551 | AAGAGTAACCAATAA[C/T]GAAAAAGAAAGACAA | 208727 |
rs33092039 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92135445 | AATAAATGAACTAAC[A/G]TGGTGCATTAAAATT | 208727 |
rs33092041 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92135113 | TACAGGTAGGTAACT[A/G]AAAAGGGCTTTAGAC | 208727 |
rs33092043 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92135093 | GAATTCTAATACAGA[A/G]ACTATACAGGTAGGT | 208727 |
rs33092065 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:92112093 | AAAACGGAACGGTTT[G/T]GCATTTTCTTTTCAC | 208727 |
rs33092067 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92111961 | AGATTCAGAGGGCAG[C/T]TCCCACAGGAAAGAG | 208727 |
rs33092069 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92111757 | CCAACATAGACTCCT[A/G]GGGCCCACAGCTCCT | 208727 |
rs33092071 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92111456 | TCACCAACAGAACTT[C/T]CTGGAAGAGACTGAA | 208727 |
rs33092073 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hdac4 | Mm_Celera | 1:92111204 | CCAAAAGCTGGAAAA[A/G]ATGATCTTCACCAGG | 208727 |
rs33092154 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92092043 | GGCTGGAACTTGGCA[C/G]AAAGCATACCTGTTA | 208727 |
rs33092156 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92090746 | TATCTCACAGGCACA[A/T]ACCCTTAGAAGCTGA | 208727 |
rs33092158 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92090715 | GCTTCTTCTCCTGGG[A/C]GTGTGGAAGAGAATC | 208727 |
rs33092160 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92090408 | GCATCTTCCCAGTGC[C/G]TGAGAACCTCTCCTA | 208727 |
rs33092162 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92090309 | CACTAGGTAAGCTTA[C/T]ATCTGCCTGAAGCAC | 208727 |
rs33092594 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92123788 | GCTGGGAGTTAAGGA[C/T]ACCCTGCTGAGGTTC | 208727 |
rs33092595 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92123512 | TGAGAAAAAAGCCTA[A/G]CAAATTCATTCCTTA | 208727 |
rs33092597 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92123360 | GTGTTCGTTGCTGCT[C/T]AACACTTGGCACAGT | 208727 |
rs33092598 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92123200 | CCCATTAGTAGCCTG[C/T]AACAACTTTCCATGT | 208727 |
rs33092599 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92122896 | TGTAAGCCCCAAGAT[A/G]TACACCCTAACAGTG | 208727 |
rs33092600 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92122672 | TGTGATGAAACTCTC[C/T]TGGTGAGCAGCTACA | 208727 |
rs33092602 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92122149 | TCTCACAGGCCGGGG[C/G]AATACATCAGTAAAT | 208727 |
rs33092714 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92077797 | GGGCTTGTCACACTA[C/T]GCACATTTTCATGAG | 208727 |
rs33092716 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92077765 | GCTGCTTCTCCAGTC[A/G]GGACTCCTAGCCTGG | 208727 |
rs33092718 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92077355 | CAGCCCTATTCAATA[G/T]AGAGGCTACTCAGCC | 208727 |
rs33092720 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92077120 | TAGTGCCCATACTGT[A/G]CAGAATGAGAGCTTA | 208727 |
rs33092722 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92077091 | AGGTCATCTACTACA[C/T]TGCCTAGGCTGCCTA | 208727 |
rs33092865 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92111134 | CCTTCCAGGCCAAGC[C/T]ATCCTGTTCCCAAAT | 208727 |
rs33092867 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92110281 | TTGCAATTCAATCAC[A/G]AACTTACTTCTAGCC | 208727 |
rs33092869 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92109262 | GTGGGTCCTATTTAA[C/T]CCTGAATACCCATAA | 208727 |
rs33092871 | snp | A/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92108938 | GCAGGTACTCTAGAA[A/T]TGAACTGTGGCTGCA | 208727 |
rs33092875 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92133454 | TGGAATTAAGAAAGA[A/G]CACAACTTCATCATA | 208727 |
rs33092934 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92090098 | GAACAATACAGGATG[A/C]AGAAGCCAGCTGCTA | 208727 |
rs33092936 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92090000 | CCATGATCAATTGTG[C/T]TCCACGTGAGGACAA | 208727 |
rs33092938 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92089190 | ACAGCCCCGGAAAGA[C/T]GTGCTTGAGAAAGTA | 208727 |
rs33092940 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92089123 | CTCAGACTCAATAGC[G/T]GTCAACACCAGAATC | 208727 |
rs33092942 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92088329 | GTCCAAGCGTTCTGC[A/G]TCTGCAAGAGCCAGG | 208727 |
rs33093584 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92077018 | ACATCTGAAGGACCT[A/C]CAGGAGACAAGGCAC | 208727 |
rs33093586 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92077015 | GGAACATCTGAAGGA[C/T]CTCCAGGAGACAAGG | 208727 |
rs33093588 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92075696 | GGTGAAACCTAGTTA[A/G]AAAGGGATTAGTTTT | 208727 |
rs33093590 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92075650 | AAATAATTAGGAAGA[A/G]ACAGGAGAAAGAGGC | 208727 |
rs33093592 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92075423 | TATCCACTATACACC[A/G]TGTGCACAGTTCCCT | 208727 |
rs33093594 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92122148 | CTCTCACAGGCCGGG[G/T]CAATACATCAGTAAA | 208727 |
rs33093596 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92122125 | AAGGAGCCAAGAAAG[C/T]AGCATCTCTCTCACA | 208727 |
rs33093599 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92121435 | CACAGGCCATCCATC[C/G]TACAGACCAGCAGCC | 208727 |
rs33093601 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92121425 | GTAAGACACACACAG[A/G]CCATCCATCCTACAG | 208727 |
rs33093714 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:92088322 | ACAGCAAGTCCAAGC[A/G]TTCTGCGTCTGCAAG | 208727 |
rs33093716 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92088240 | TAAATAATATCAGCA[C/T]GAGAGAAGCCTTTCC | 208727 |
rs33093718 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92088087 | CTATCTACAGGGCCA[A/G]CCTGAGAAGCACAGA | 208727 |
rs33093720 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92088040 | CCTGGGTCACAGCAC[G/T]AGGATACAAGCTAGG | 208727 |
rs33093722 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92087406 | AGTACTTGTACCTAG[A/G]ACCCTCAGCATCATC | 208727 |
rs33093744 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hdac4 | Mm_Celera | 1:92108803 | TCAGCCTGTTCTGTG[C/T]AGGCACAGTCACTGA | 208727 |
rs33093746 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92108610 | CAAAGGAGGAGAATT[C/T]AGGAGGTAGCATTCC | 208727 |
rs33093748 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:92108572 | TAGGCAGAAGCAGGT[A/G]TGGACAGGAGCAGCT | 208727 |
rs33093750 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92108262 | TCCTGAGGCTGGAAC[C/T]CAAAACCTGAATTCT | 208727 |
rs33093752 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92107755 | ACTGTTCCTCCTCCA[A/G]GAGTGGACTGGAGTA | 208727 |
rs33094264 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92075009 | CCTTTGAAGGTGTCT[C/T]CTTTCAGAACAAAAG | 208727 |
rs33094266 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:92074795 | CCTTCATACCCACCT[A/G]GGGTCCTGTGCCTCA | 208727 |
rs33094268 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92074769 | GTACGTGAAGCCAGT[A/G]CATGACCACACCTTC | 208727 |
rs33094270 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92074484 | AGGCTTAGGACACTC[A/G]GTCTGCCCATAAGTC | 208727 |
rs33094314 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92107576 | CTACAGTGCCTTTGA[A/G]ACAGGTAGCAGTCAC | 208727 |
rs33094316 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92106809 | TTTCCTCATGGATAG[A/T]AGAACTACAATCACA | 208727 |
rs33094318 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92106538 | TGGGCTGTCATTCAT[A/G]TGGCTCTAAGAAGGG | 208727 |
rs33094320 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Hdac4 | Mm_Celera | 1:92106506 | GTGATCTCAGAACAG[C/T]AAGCACACGCGGTGC | 208727 |
rs33094344 | snp | C/G/T | 0.260355 | 0.249785 | intron-variant | Hdac4 | GRCm38.p3 | 1:92086825 | CCAAAGGGTTACACA[C/G/T]AGGGCACTCATCAAA | 208727 |
rs33094346 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92086803 | AGAGGTGCCAATGCA[C/G]CTACTGCCAAAGGGT | 208727 |
rs33094348 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92086740 | AAGTTATTTTATGCA[C/T]CATGGAAGGAAGGAC | 208727 |
rs33094350 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Hdac4 | Mm_Celera | 1:92086355 | GGTATGAGTCTGCTT[A/T]GTCTGCTGTGACTAA | 208727 |
rs33094352 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Hdac4 | GRCm38.p3 | 1:92086258 | GACAGAAACAGAGAT[A/T]AATCCACTTTGACCT | 208727 |
rs33095034 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92085635 | TGGAAGATACAATGG[A/G]ACAGATGAAGGGAGC | 208727 |
rs33095036 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92085084 | GATCGTACCTGCAGG[A/G]TGAGAAGCTGAAGGT | 208727 |
rs33860094 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91956934 | CTCTCTCTCTCTCTC[C/T]CTCTCTCTCTCTCTC | 208727 |
rs45635927 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | GRCm38.p3 | 1:92039850 | GCATGCACAACACAG[A/C/T]GGCATGGCCTGAGCC | 208727 |
rs45647864 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91974148 | TCCTAAGAACTGTCT[C/T]ATGCTTGGAGCATCT | 208727 |
rs45652237 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92000320 | GACTCCCTTCCCTAT[A/G]CCGCAACTCCTCAAC | 208727 |
rs45656757 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92037434 | ACACCGCCTTTTCTT[C/T]TGGAACTTTGAATGC | 208727 |
rs45658957 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92042887 | AAGGCTCCCGACACA[C/T]GCCAAGCCAGCTACC | 208727 |
rs45669242 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91984794 | TGTAGACAGAAGACA[C/T]TGTGACCGTCAGAGT | 208727 |
rs45683128 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92063374 | AAACACACAGCATGT[C/T]CACAGAGGAACATGT | 208727 |
rs45684865 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Hdac4 | Mm_Celera | 1:92004111 | CTTGGAGGGATCATG[A/T]ATTCATGGAACTGTT | 208727 |
rs45696007 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91942695 | CCTGACCAGAGACAC[C/T]AGCCTGCCAGCCCTG | 208727 |
rs45702710 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91990806 | CACAGTCACTGAAAC[A/C]GACTGGACCAACTAG | 208727 |
rs45707187 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91972296 | GGAGAGAGGTCCAGA[A/G]TCTGCTCTGCTCCAG | 208727 |
rs45765842 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:92016487 | GGCTTGGTCTATCCT[C/T]ACAGAAGCACCACAC | 208727 |
rs45766296 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91970929 | AGGGGTCTCTGTCCC[C/T]ATAGACCCCATACCT | 208727 |
rs45794738 | snp | A/C | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92038848 | CATGCCAGCTACAGA[A/C]ACTGGCTACCTGCCC | 208727 |
rs45821532 | snp | A/T | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Hdac4 | GRCm38.p3 | 1:92031584 | TGACTTTGATCAGAG[A/T]CCTAAATGTGGCTAT | 208727 |
rs45829866 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91977235 | GTATAAGCACTGGGA[C/T]GCAGACAGCAGGTCA | 208727 |
rs45831058 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92045663 | TGTGCTAGCTTTGCA[A/G]AGATGTAGCAGATGC | 208727 |
rs45840892 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91945218 | GGGCTCCCAGGGTTA[C/T]GTGACATCACCTTCA | 208727 |
rs45861162 | snp | A/G | | | intron-variant | Hdac4 | Mm_Celera | 1:92011899 | CGCAGCCTTGCTAGA[A/G]GAAGTATGTCATGGG | 208727 |
rs45873806 | snp | A/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91957773 | ATCCAGCCTGGCAGA[A/T]GCCCAGATTGCCTCT | 208727 |
rs45879702 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91954389 | ACTTGCATACATGCA[C/T]ACACACTTGCTCAAA | 208727 |
rs45888437 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91946766 | TGCCAGGACCTTGAC[C/T]GAAGAAGGCATTTGT | 208727 |
rs45919316 | snp | A/C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | GRCm38.p3 | 1:92062658 | ACAGGTGTAAGAAGA[A/C/T]GACATGGCGGAGAAT | 208727 |
rs45942893 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Hdac4 | Mm_Celera | 1:92018464 | TTTTGAGCCACATAC[C/T]TAACTCAAACTTAGT | 208727 |
rs45947256 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91947182 | CTCATGCCCACAGTA[C/T]AGCTGACAGAACTGG | 208727 |
rs45955824 | snp | G/T | 0.497778 | 0.0332592 | utr-variant-3-prime | Hdac4 | Mm_Celera | 1:91931889 | CATATGTGCATGGAG[G/T]CTTGGCGAGGGCAGA | 208727 |
rs45969530 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Hdac4 | Mm_Celera | 1:91943358 | ACAATCAGCTGTAGG[A/C]TGAGCCCCCTGCCTT | 208727 |
rs45980206 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91978418 | GTGCCTGATGCTGGG[A/G]AGGCCCAGACTTCCC | 208727 |
rs45988855 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91935524 | TCACCAACAAAAGAA[A/G]TAATGACTGATGCCA | 208727 |
rs45994349 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92050233 | TACACAAGTAACATA[C/T]TCAAGTATCAAAAAG | 208727 |
rs45995763 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:92017708 | CACTGAGTGTAGAAT[C/T]CAGACCATAATAACA | 208727 |
rs46003498 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91969534 | ACCTATACTGATGTG[C/T]AGGACTGAAGGGATT | 208727 |
rs46025498 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92065096 | GCTGACCAGGTAGTA[A/G]ACCAACTTCCCATGC | 208727 |
rs46029042 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91999991 | TGCTGGATATGGTTT[A/G]GCTCTCTTCTGCCAT | 208727 |
rs46030035 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92005364 | CACAGACTGACTGGC[C/T]GATGTTTAAAATTTG | 208727 |
rs46042365 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92018221 | GGCTACTGTTGTGTG[C/T]CTCTTGGTATAAAAG | 208727 |
rs46077350 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92062974 | ACAGAACTGCCCTCC[C/T]GCTGGACTTCCTCCT | 208727 |
rs46101845 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92065211 | CCTCCTGGCTAGTTG[C/T]TGAGCAGCTGGAGGG | 208727 |
rs46117977 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92028441 | GTCCTGGAAAACAGG[A/G]CCCCATGGGAGGTGG | 208727 |
rs46120654 | snp | A/G | | | intron-variant | Hdac4 | Mm_Celera | 1:92122242 | CACAGGGCCTCCCAT[A/G]CTCCCAACCATGGAA | 208727 |
rs46138129 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:91948650 | CAACTGTGTCTCATA[C/T]CCTTTCTAGCATATG | 208727 |
rs46149438 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91951522 | AACCGCCTGGGCTGG[C/G]AGCCCGTTATTAGAG | 208727 |
rs46178104 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91947572 | CATCATCGGATCAGC[A/G]AAAAACATGGGATGC | 208727 |
rs46192069 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91993142 | TTTCCCATACATTTT[C/T]TGGTCTTGGGGATTT | 208727 |
rs46197112 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hdac4 | GRCm38.p3 | 1:92021731 | CAAGTCTCGGCAGAA[C/T]TTGAGAAGGAAGAGG | 208727 |
rs46203123 | snp | A/C | | | intron-variant | Hdac4 | Mm_Celera | 1:92010862 | AGACTTTCAATGAAA[A/C]CACAAAGTCCCAAGA | 208727 |
rs46208175 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91947296 | GCTCAGGGCTTGCTG[A/G]TGCTGTCCATATATT | 208727 |
rs46210038 | snp | A/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91972633 | TTAACCTCTCATTAG[A/T]GGCTTCCTCCACAGC | 208727 |
rs46214314 | snp | C/T | 0.132653 | 0.220748 | downstream-variant-500B | Hdac4 | Mm_Celera | 1:91928536 | GGAAACCAAACCCTC[C/T]GAGCGCACCTGGACC | 208727 |
rs46235707 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92016787 | TTGCATCCTCACTTG[G/T]CCACCCTTGTTGATA | 208727 |
rs46236682 | snp | G/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91957816 | TGGAGTTTATGACAC[G/T]TAAGCACTGTAACTA | 208727 |
rs46239016 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hdac4 | Mm_Celera | 1:91937543 | AGAATGAGTCTGGGT[A/G]AGGGATTGAAGAGCT | 208727 |
rs46240249 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92003515 | CATCCATCCATCATT[G/T]TGTCATTTCCAGTCA | 208727 |
rs46242766 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92018667 | TCTGGGTCTCTAGGA[A/T]GCTCCCATTATCCCT | 208727 |
rs46243490 | snp | A/C | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91937681 | CCAACAACAAAAACA[A/C]GAGTCGCTGGGCACA | 208727 |
rs46244140 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91955159 | TACCACTGGGACTCA[A/G]CAGGCTCTCAGAAAA | 208727 |
rs46295262 | snp | A/C | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92036367 | CATCAAGTAAAAGGC[A/C]AGAAGGAACATCGGT | 208727 |
rs46306106 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92003936 | AGCAGAGTTACTGCT[A/G]GTTACAGTCCTCTGG | 208727 |
rs46340137 | snp | A/G | | | intron-variant | Hdac4 | Mm_Celera | 1:92038701 | TTTAGTCTTAAAAAT[A/G]GATTTTATATTGTTT | 208727 |
rs46342708 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:92018901 | AGGAATGTCAGGTAC[C/T]GTGTGAGAGCCTGCA | 208727 |
rs46349107 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Hdac4 | Mm_Celera | 1:91942320 | CTGTCTAGTTCTCTG[A/C]TGGTCTCCAGACCTG | 208727 |
rs46349428 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:91938620 | TGCTTCTAGTGTCTA[C/T]GACCTGCCTCCTGCA | 208727 |
rs46355318 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91964490 | TACACATGAGGTGCG[C/T]AAGAGCTGTGGCCTA | 208727 |
rs46363836 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hdac4 | GRCm38.p3 | 1:91984265 | ATCACATTACAGAGA[A/G]CCATAGAGTTTCTAC | 208727 |
rs46364069 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92037197 | GAAATGAGAAGGCAC[C/T]CATGATCCATATCTT | 208727 |
rs46369899 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92056856 | AATTTGCTGTCTCAG[C/T]TCAAATAACAATACA | 208727 |
rs46401918 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92012486 | ACACCTGGATGGTCA[A/G]AAACAGTGCCACTGG | 208727 |
rs46404442 | snp | A/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:92017922 | GAGAATATGCTGGCA[A/T]AGGCTCACATACTGG | 208727 |
rs46415359 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:92034484 | GCCTGTTACAAGAAA[A/G]CCACAATCACGCTTG | 208727 |
rs46422654 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92002415 | TCTATCTAAGCACTG[C/T]ATGAGTGCACTCTAC | 208727 |
rs46428624 | snp | A/G | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91936687 | ACAGTGATCAGGAGG[A/G]AGGCCAGGAAAACAT | 208727 |
rs46434848 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91956334 | AGCACATAGTGTAGT[C/T]CTGACTTCAGTGAAA | 208727 |
rs46446141 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91934825 | TGAAGTAACTCTAAA[A/G]AGCCAGTATGACTTG | 208727 |
rs46450721 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91954155 | GAGATATGTCACTTC[A/T]AGGAACTACTGATGA | 208727 |
rs46464928 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92001350 | AAGCCTTTTTTTTCT[C/T]AATGCTGGGCAAGTC | 208727 |
rs46467732 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Hdac4 | Mm_Celera | 1:91928419 | GCCAGGGACATCCAC[A/G]CCCTGCCTGTAACTT | 208727 |
rs46500014 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92048006 | TGGGTGATAGCACTG[A/G]AGAAGCATACAAACA | 208727 |
rs46502704 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Hdac4 | GRCm38.p3 | 1:91956147 | CTGCTGGGTCCCATT[C/T]CCATGATGTACATCC | 208727 |
rs46508633 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Hdac4 | Mm_Celera | 1:91992174 | CTTCTCTGCACTGAG[C/G]CTTCTCTGCACTGAG | 208727 |
rs46509713 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92037931 | AAACAAACCTTTAGT[A/G]GACACCTTTAGAAGG | 208727 |
rs46512277 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92058675 | TAAAGTATGCAGTGT[C/T]AAAACTCTTGAGCTA | 208727 |
rs46513899 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:92022260 | GCTGGAATGGGAGAT[A/G]TCCCGTGGGCCAGAG | 208727 |
rs46531188 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91952195 | CTTGTTACTGTTTAA[G/T]GAGGTAGTCTCATCT | 208727 |
rs46551376 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91969552 | GACTGAAGGGATTTT[C/T]CTAGCTGAGGAGAAG | 208727 |
rs46558553 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92054637 | TTCAGCAAACTATAC[A/T]TGAGGGAAAGTGTAA | 208727 |
rs46567478 | snp | A/T | | | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92114621 | TTGTGGGAAAGCTAA[A/T]AAAAAAAAAAAAAAA | 208727 |
rs46599161 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91966396 | CACAGCAGTATTTAA[A/G]CATCTAATTAGGGCT | 208727 |
rs46599552 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91967583 | TGAGCACAGCATCAA[A/G]AGCTTGGAGAACATG | 208727 |
rs46603707 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:91979224 | TGGGGAAGATGTTCT[A/G]GGTATAATTTCTGAC | 208727 |
rs46607798 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91944175 | TCAGTGCTTGGTTGA[C/T]GTACTCAGGGCCTGA | 208727 |
rs46629149 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92021746 | TTTGAGAAGGAAGAG[A/G]TAGGACATAACCAGT | 208727 |
rs46644511 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91987122 | GAGTCATGTTGGACC[C/T]GTCTTCTCTTTTCTG | 208727 |
rs46650322 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92040463 | TCATAGCTAGTGATC[A/G]CCAAACCCAGAAAAG | 208727 |
rs46656070 | snp | A/G | | | intron-variant | Hdac4 | Mm_Celera | 1:91945665 | CCACACGAGTGAAAC[A/G]GGAAGGGAGAACGTG | 208727 |
rs46661712 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91983833 | CTGGAACATGGACAA[C/T]GCCAGTTCTAGGATT | 208727 |
rs46661726 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91945634 | GCAGCATGAGGCCTG[A/G]CCAGCACGTTATCCT | 208727 |
rs46663081 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91988069 | AACTCAAGCAACCTA[C/T]GGAAACTGCTCAGTT | 208727 |
rs46678097 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92037145 | AGGTGATGAGGCCTC[C/T]TCCCTTGGCACAGAT | 208727 |
rs46695301 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92035773 | CAACAGAAGCTGTTG[A/G]TGCTTTTGACCTAGG | 208727 |
rs46713211 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91938818 | TTCCCTTTTTGAGAA[A/G]ATATTGCCCCATGAA | 208727 |
rs46764161 | snp | G/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91957223 | CATCATGCATTTTAA[G/T]ACAAAGTGTGGCCCT | 208727 |
rs46774797 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91983557 | ATGAAGCCCATGGTC[C/G]CTGGCTTCCAAGAGA | 208727 |
rs46785655 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92017172 | AACTTTTTACCTGCT[A/T]TAATCACCTTTGGAA | 208727 |
rs46799088 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91933865 | GACTCACTTGTGTCT[A/G]AAAAGCGCCTTTCTG | 208727 |
rs46799333 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91958127 | CCTCACTATGGGCAC[A/G]ATCCTGCAGGTCAGG | 208727 |
rs46800397 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92033185 | CGACAGGCCAATCAT[C/T]CCTGCCAGTGAACCC | 208727 |
rs46807957 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92030907 | TCAGGGCTTACAAAA[C/T]TGATTCCAAATTAAA | 208727 |
rs46823555 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:92044752 | GAAGCTATAAGAAGA[C/T]TCTAGGAGTCCTAGC | 208727 |
rs46845378 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91991697 | TTTAAAATATGCACA[C/G]CTGGTAAATCTCCAC | 208727 |
rs46848130 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91989208 | CTTAGACACAAACTC[C/T]TGCTAAGTATGCAGA | 208727 |
rs46854606 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91938564 | TGGTACCCAAAGCCC[C/T]CAGCAAAACTCTCCA | 208727 |
rs46860770 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92037857 | CTTAGAGAGGTCTGT[A/T]GCTACTTGAGCCCTG | 208727 |
rs46861859 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91996354 | CCACAGCCCCTGACT[A/G]TGTGACCGAGGGCCC | 208727 |
rs46864543 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91993171 | TTTGTGATTGCAACA[G/T]AAAATAGACCAGGAC | 208727 |
rs46907265 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92041876 | AGGTAAGAGACAAGC[A/C]GAACCACAAGAGACA | 208727 |
rs46918732 | snp | C/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92031978 | ACACAGATCCTCTTG[C/G]TACCCATCAACAGGT | 208727 |
rs46920072 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92042758 | CTAAAGACTTTCACA[A/C]AATGTTATTGAAAAC | 208727 |
rs46932066 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91983115 | GTTCACAGGTCTGGG[C/T]TCTACACACAGTATT | 208727 |
rs46939136 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92012323 | GTGTGGGACACAGCA[A/C]TGTCCTCAGAGTCGG | 208727 |
rs46960649 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | Mm_Celera | 1:92016968 | CTTTGTACTAAGCTT[C/T]ATTCCAAGAGACTAC | 208727 |
rs46969070 | snp | A/C/T | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:92011205 | CAAAAGGTCAACCCT[A/C/T]GAAGGGAGAAAAGGG | 208727 |
rs46982195 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91972067 | GAAATATTAAATCAA[C/T]AATACAAAGAATCAC | 208727 |
rs46990886 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91972693 | CAAGCAAGAGGTCAT[G/T]AGTTACCTGTGGTGA | 208727 |
rs46993371 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91986664 | TTTCCAGACATAAAG[A/G]GGTTAGAAACCTGAC | 208727 |
rs47020467 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92036778 | CAGCTGAGCAGCCTC[C/T]GAGAAAGCAGTATCC | 208727 |
rs47020950 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91937562 | GATTGAAGAGCTGGA[A/C]GTGACCAAGGTCCCA | 208727 |
rs47029410 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91971826 | TCATTGCAGAGTTTC[C/T]CTTATCTGAGCTGCA | 208727 |
rs47037624 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92047044 | AAAGAAAAAGTTCTT[A/C]AGGAAGCCCCAAGAA | 208727 |
rs47038843 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91957618 | TGTTATGAGACATCA[A/G]TACTAAAGAGTTTCT | 208727 |
rs47039701 | snp | C/G | | | intron-variant | Hdac4 | Mm_Celera | 1:92142366 | GCCAGTGCAGGCCTT[C/G]TGGGGGGACATCTCC | 208727 |
rs47045972 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92038144 | TCCACCTTCCAAGAT[A/G]TGGCCTGCATGCCCC | 208727 |
rs47052440 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hdac4 | Mm_Celera | 1:91944850 | ATAAATTAGGTAACA[A/G]ATATACATACCAGCC | 208727 |
rs47053575 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92006075 | TTACTGATAATTCTA[A/G]CTGTTAATTTTGTAA | 208727 |
rs47054967 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91957110 | GAGCCTTTCATGCCA[C/T]GCACCAGGTTCCTGG | 208727 |
rs47057794 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91971958 | TAGGAAGTTTCCTTC[G/T]AAGAAAAGAACATGA | 208727 |
rs47078152 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91949989 | CACTCCAATAAGTGC[A/T]TATGAAGGGCTTTAG | 208727 |
rs47092156 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Hdac4 | GRCm38.p3 | 1:92024318 | AAAAGTAGGTGACTA[C/T]TCTGTATCAAGTGAG | 208727 |
rs47102815 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91936883 | AGGAAAACAGATCAT[C/T]TTCACAGCAAGGGAA | 208727 |
rs47108778 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | GRCm38.p3 | 1:91964497 | GAGGTGCGTAAGAGC[C/T]GTGGCCTAGTAAGAT | 208727 |
rs47125790 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92051937 | GCGACATCCTGTGGT[A/G]GACAAGGAGCATTTC | 208727 |
rs47138353 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:91945777 | GGCTGGGATACAGCT[A/G]TAGCCCCGTGCTGGG | 208727 |
rs47146184 | snp | A/G | | | intron-variant | Hdac4 | Mm_Celera | 1:92122059 | TTTTAATAGTATTTT[A/G]TAATTAAATTTAAAT | 208727 |
rs47154108 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91960705 | AGCTCTGGGAAGCCT[C/T]TCTGCATGTCACTGT | 208727 |
rs47169826 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91990787 | GTTTTCCCCTGGACA[G/T]CAGCACAGTCACTGA | 208727 |
rs47182134 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91974820 | CCCTGGCTTCTAACC[A/T]AGGGCTTTCTAGACA | 208727 |
rs47186820 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91945135 | GGTTGAGAACCATTG[A/G]CCTAGACAGATTCAG | 208727 |
rs47198509 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91934757 | TATATATTAAATGGT[A/G]TCTACTAGAGACAGC | 208727 |
rs47200903 | snp | G/T | | | intron-variant | Hdac4 | Mm_Celera | 1:92113174 | CACTGAGCAGTTATA[G/T]AACAGAACTCAGGAA | 208727 |
rs47203101 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91951141 | ATGGGAAGGTCAGTA[C/T]CAGGCATAATCTAGG | 208727 |
rs47203703 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91949584 | CCCAGTGCACACACT[A/G]GAATTTGTCTAGAAA | 208727 |
rs47209724 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:91936011 | GTGCAATGTTAAGAG[C/T]GGCCTCACAGGCCAT | 208727 |
rs47232811 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91966985 | CTAGCTGGCTCTGTC[C/T]TGCTCCTGTGTGGAG | 208727 |
rs47235908 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92026274 | CCCTGGCAATTTCTG[A/G]ATTAAGTTCATCTTG | 208727 |
rs47260473 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Hdac4 | GRCm38.p3 | 1:91953555 | GCTCACCTCAAAGGC[C/T]GGCCAGGAAGTTCAG | 208727 |
rs47281583 | snp | A/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91963269 | TAAGGATTGGTTTTT[A/T]ACATTCTAAAAGAAC | 208727 |
rs47296710 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91966061 | TGCACAACGCGCATG[A/C]CGTCTAGCCTTAAGG | 208727 |
rs47297463 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91951767 | TTATACCTAAAGCAT[C/T]CTGTCCTAATGCACC | 208727 |
rs47300730 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91996338 | AAGTAAACAACAGTG[C/T]CCACAGCCCCTGACT | 208727 |
rs47319299 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92049442 | CAGGTCCCATCCACA[C/T]TACCCAACATAGTTG | 208727 |
rs47324912 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92055433 | ATCATTTCTTTGAAA[G/T]TCACTTTTAGATCAT | 208727 |
rs47326186 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92000955 | TAGCCTGCTTCAGAA[A/G]ACATGCAGTGTGTAC | 208727 |
rs47332273 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92016164 | TGGAGAGGGTACAGG[A/G]ATTCCCCATAACAGC | 208727 |
rs47334873 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92033170 | TTAACTTCAAGAACA[C/T]GACAGGCCAATCATC | 208727 |
rs47336476 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91971240 | TGGTACGAGAGGATC[G/T]TGATAAAAGCATAGT | 208727 |
rs47363393 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92025998 | AAGACATGCAGGAAG[C/T]GTGGGAGAGGATAGT | 208727 |
rs47365571 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92037907 | TGGAGGCACCTGGCA[A/G]TCTGTAGCAAACAAA | 208727 |
rs47367174 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91969978 | CAATGTCTGCCACAC[A/G]GCTCCTTGGGTAGAG | 208727 |
rs47382092 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Hdac4 | Mm_Celera | 1:92018465 | TTTGAGCCACATACT[C/T]AACTCAAACTTAGTT | 208727 |
rs47383765 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91952447 | GTTGAGAGCCAACCT[C/T]TGCATCACAGATGTA | 208727 |
rs47424248 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Hdac4 | GRCm38.p3 | 1:92034593 | TCCCATTGCAAATCC[A/G]GCACTATAGCTCCTG | 208727 |
rs47429101 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92039324 | CAGATACTTAAATAG[C/T]CCTGTCCTCAGTCAC | 208727 |
rs47433133 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Hdac4 | GRCm38.p3 | 1:92030341 | TGGTGTCCCTTGGCC[A/G]AAGGCCTGGTAGGCT | 208727 |
rs47441583 | snp | C/G | | | intron-variant | Hdac4 | Mm_Celera | 1:92011917 | AGTATGTCATGGGGT[C/G]TCTCTCTCTCTCTCT | 208727 |
rs47442080 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hdac4 | GRCm38.p3 | 1:91937891 | AGACACAGCAGATAA[A/G]TCAAGGCGGGAAGCA | 208727 |
rs47458515 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91950422 | TCCCTGCTGTCCTGT[A/G]GATGTGCCTCCTACC | 208727 |
rs47461424 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92015945 | AAGAGGTTAGAGCCT[C/T]AAGACTTCTCAGAGC | 208727 |
rs47463279 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Hdac4 | Mm_Celera | 1:91950025 | AGTTTTTGAAGTATA[G/T]CTGAGCTATTTAATA | 208727 |
rs47469178 | snp | C/T | | | intron-variant | Hdac4 | Mm_Celera | 1:92129238 | ACACACACACACACA[C/T]ACACACACACACACT | 208727 |
rs47470225 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92055626 | CCTTTAAAAGCACCA[C/T]GTAAAAGGTTAAACG | 208727 |
rs47489912 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92022173 | CAAGTGTTAAAAAGA[C/T]AAGCAGGTGCACCGT | 208727 |
rs47491109 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92028261 | TAAGAGGCACAGATA[G/T]GTGAGGCTATGGCTC | 208727 |
rs47498234 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92014094 | GGAGACAGTCTAGAA[C/T]TGAACGTCCAGCTAC | 208727 |
rs47498555 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92037695 | TTCAAGAGTAGTGTT[C/G]TTTTCTTGCAGTCCC | 208727 |
rs47502591 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91971231 | TTTCCAAGCTGGTAC[A/G]AGAGGATCGTGATAA | 208727 |
rs47502868 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:92056219 | AAAACCAACAATAGT[C/G]TCCTCGAACTTTATG | 208727 |
rs47506867 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92048409 | GACCTGCTTACAACA[A/G]CATATATCTCAAACT | 208727 |
rs47525873 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91970166 | CGGGCTCATGAAGCC[A/G]ACAGGGCTGGTGGGA | 208727 |
rs47532683 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91949903 | ATCACGTTTTTGACA[A/T]GGATTTTAAAGCCAA | 208727 |
rs47539827 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91973290 | TCTCCACAGGTTCTT[C/T]TGGTAGTGAAAGGGT | 208727 |
rs47540450 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91936491 | CCATTTAGATTAGCA[C/G]AGACTGCAATTATAC | 208727 |
rs47547999 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92026072 | GTTTCTCAGGCCCTC[A/G]GAGAAGTGGTCACTG | 208727 |
rs47551316 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:91948304 | ACTGAGATGTTCAAC[G/T]GTCAAGCCATCTAGC | 208727 |
rs47554568 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91974423 | TGAATTCTACTAGAC[C/T]GTAAAGAGCAGTGTT | 208727 |
rs47570122 | snp | C/T | 0.497778 | 0.0332592 | utr-variant-3-prime | Hdac4 | Mm_Celera | 1:91931964 | GAAGTTGCCCAGGGG[C/T]GAACATGCTGGCAAT | 208727 |
rs47618198 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92038746 | TAAGGGCAGGCACTG[C/T]CAGCAAACTGTATCT | 208727 |
rs47621203 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91949747 | AGGCCTGAGTCTTGG[C/G]TCTTCCTTGGTGTGC | 208727 |
rs47628448 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | Mm_Celera | 1:92017119 | GTGTCCACAGGTAAT[A/G]CACCCTCAATGGGTC | 208727 |
rs47641450 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91961384 | ATCCTGGACAGGAGC[C/T]TCCTCACAGAGGGCA | 208727 |
rs47652137 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92053681 | GTGTCATCACCAGAA[C/T]TTTCATGAGTTCATA | 208727 |
rs47655721 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92040559 | TCATAGCTCAGCCAG[C/G]GCAGCAGTTTTCAGG | 208727 |
rs47660444 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91951243 | AGTGCAAGAGCTAGG[G/T]GATGCTCTCACATGA | 208727 |
rs47677658 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Hdac4 | Mm_Celera | 1:91953484 | CGCTCTCAATAAGGG[A/G]TTATCATTCATACAC | 208727 |
rs47680774 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91993883 | CATTTAACGGTTGGG[C/T]GGAGCGGAGGGTAAG | 208727 |
rs47688461 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91946136 | CAGTAACTGAGGCTC[A/G]CTTAACATGCTTATT | 208727 |
rs47690074 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91936920 | GGTAGTGGGTTGATA[C/T]TGCTATGTGCCAAAA | 208727 |
rs47694071 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92037265 | CAGATCTGGACCCTG[C/T]ACCACGACTTCCTTT | 208727 |
rs47702709 | snp | A/C | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91956797 | CTTAAGACTTGATGC[A/C]CATTTATCAAGAGGC | 208727 |
rs47710001 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92011344 | GAACACTCTCTGGAA[G/T]GGGAGCTCTGCCAGG | 208727 |
rs47722960 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:92034575 | CTGTACAGCACTGAG[A/T]CTTCCCATTGCAAAT | 208727 |
rs47731094 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | GRCm38.p3 | 1:92020788 | TTCCTGGCTGTTCCC[A/G]ACACAATATTTTATG | 208727 |
rs47744695 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91962686 | TCTCTCCAGCTTGAG[A/C]TTGACTTTATTAAAG | 208727 |
rs47754926 | snp | C/T | | | intron-variant | Hdac4 | Mm_Celera | 1:92113096 | AAGTAGCACTGTGAA[C/T]AATGGTCCCCCAGAA | 208727 |
rs47774303 | snp | C/G/T | 0.486111 | 0.0821678 | intron-variant | Hdac4 | GRCm38.p3 | 1:91960020 | CTGACTGCAGCTTAG[C/G/T]TGTTGGGGAAACAGA | 208727 |
rs47779162 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hdac4 | GRCm38.p3 | 1:91937809 | TCTTCAGTTCACCCA[A/G]AGAACGGGACGAATG | 208727 |
rs47784514 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92043532 | GATCTAGGACCAAAT[A/G]CTGTGGCTAGGCAGT | 208727 |
rs47790735 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91941676 | ACTCTTTGTCAGGTG[A/G]TGGAATTAGAATCAT | 208727 |
rs47827963 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92023601 | GTCTAGAGCTCAAAG[C/T]AGGGACTGTCCCACA | 208727 |
rs47829391 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92013951 | TTGATGTTGCTCCCT[C/G]ATAGAATGAAGAGTG | 208727 |
rs47852025 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91945423 | CAGGCCAATGTCCCC[A/G]ACTCTGCCTGGCAGT | 208727 |
rs47857599 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92048587 | CACAGAATTTCGGAA[C/T]TTCCTTCTTAGCAAC | 208727 |
rs47860880 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:92012944 | CTACAGAGGAAGACA[G/T]GGTGCCAAGGCCTAA | 208727 |
rs47861146 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91979092 | AGTAAACCACCCATA[G/T]CAGTCCAAGTTCTCA | 208727 |
rs47864906 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91935432 | AGGAAGCATGACCTT[C/T]CAACCAAAGACTTTT | 208727 |
rs47878111 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91945878 | GGTGAGCACACTCTG[C/G]AGGGCCAGGACCGCT | 208727 |
rs47894404 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91940714 | AACTATGAGGAACTA[C/T]AGAGAGACGCAGGCT | 208727 |
rs47895318 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92066577 | CCCCAGCACTCAGGG[C/T]TCCATAAGAGGATGC | 208727 |
rs47895729 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91998401 | AGTGAAAAAAGGCAG[C/T]TCTTGTCTTACTCAA | 208727 |
rs47898037 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92017530 | ACTAACCAGATCTGT[A/G]TTCCTCAGCCCATTA | 208727 |
rs47904455 | snp | C/T | | | intron-variant | Hdac4 | Mm_Celera | 1:92122590 | CAGAGTACTAACTTC[C/T]GTGACCCTTCTTATT | 208727 |
rs47936037 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92003614 | ATGTAGTGTGCATGC[C/T]ACATCTTCCCTCACC | 208727 |
rs47954309 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92055256 | TTTACTGCAGAGACC[A/T]CGAGCATTAAAATCA | 208727 |
rs47957613 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hdac4 | Mm_Celera | 1:91948431 | TGTCATTTTAGGGGC[C/T]AGCAGGGACCCTGAG | 208727 |
rs47963105 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92028109 | CAAGACCTGAAATCA[C/T]AGAGAAGGGACAGAC | 208727 |
rs47969781 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91938665 | CTGTGCAGTGCCATG[A/G]CTGAGCAGACCACCC | 208727 |
rs47970793 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91966654 | GAGTCCACCACACAG[C/T]TGCTGGGACGCAGGG | 208727 |
rs47976245 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91937079 | GATATTCTTGAGACC[C/T]GGTAAGAATGTCCTG | 208727 |
rs47982175 | snp | C/T | 0.408163 | 0.193609 | downstream-variant-500B | Hdac4 | Mm_Celera | 1:91928697 | GGCATGGGAGGTCAG[C/T]GCCCAGTGTCCTGGG | 208727 |
rs47988212 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hdac4 | Mm_Celera | 1:91962193 | TTTCCACAAGCTTCA[C/T]TCTCAGAAATAGATG | 208727 |
rs48014491 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92012257 | CTGCATGTCCACCTA[C/T]TGGCCAATACCTACT | 208727 |
rs48017364 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Hdac4 | Mm_Celera | 1:92009588 | CAAAGAGAGCTCAGC[A/C]TCAGGCCAACACTGC | 208727 |
rs48026492 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91950114 | CAAGAGTACTGATGA[C/T]TACAATTGCTGTGTG | 208727 |
rs48036728 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92033120 | TAGCAGCTCTTTCAA[C/T]ATCAAGTATACAACC | 208727 |
rs48043487 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91949130 | TGGATTTGGCTTCTG[C/T]TGCTCTGGAGGTGTA | 208727 |
rs48049466 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92015088 | GTAAACACGTGTGAA[G/T]ATGGTTCCACTTCAC | 208727 |
rs48050843 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91953891 | ATATCTCCAGTGCTG[A/C]GGAGAGAGCCAGGCT | 208727 |
rs48059926 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91937347 | GTAGACTTCAGAGAG[A/G]CCATTGTGGTCCAGG | 208727 |
rs48062292 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Hdac4 | GRCm38.p3 | 1:91990231 | TGGGGGTGTGTGGCA[C/T]TCAGAGGAGCCTGAC | 208727 |
rs48072308 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91960669 | GTGGTGGTTCTGAGT[A/G/T]TGGAAGGCCATGTAT | 208727 |
rs48088360 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91961929 | CACAAGGCGTAAAAA[C/T]GAACTCTTAGGTCTG | 208727 |
rs48090659 | snp | C/T | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Hdac4 | GRCm38.p3 | 1:92031158 | GTATACACACAAAAT[C/T]TTAAAAACACAATAA | 208727 |
rs48108418 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92021818 | GTATTTGCTTAAAGC[G/T]ACCAATGCTCAGTAT | 208727 |
rs48118218 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:91993104 | TCCTGGTTTACAGAA[C/T]CAAGAGCCAGCTAAA | 208727 |
rs48118917 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Hdac4 | Mm_Celera | 1:91928889 | CCGCCAGAGGACACC[A/G]CCGGTCAGTGAACCC | 208727 |
rs48122030 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91965533 | GGAGGCAGAACAGGA[A/T]CAGTAAATCCATCTT | 208727 |
rs48137459 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hdac4 | GRCm38.p3 | 1:92035138 | TGGAGGATTGAAGAA[A/G]AGAGGCATCACTCCC | 208727 |
rs48140826 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91939745 | AGAAAGCTTAGACAG[C/T]TGGTAACAACATCAG | 208727 |
rs48140884 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92024095 | CAAGCCCAGGAAACT[C/T]TTGGCAGAGGGACAC | 208727 |
rs48146022 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92047780 | CAAGGGGCCACCTGG[C/T]GATGACTAGCCATCT | 208727 |
rs48154121 | snp | A/C/T | 0.486111 | 0.0821678 | intron-variant | Hdac4 | GRCm38.p3 | 1:91970875 | AGAGAATATGAATAC[A/C/T]GCAGGCTGGAGGCCA | 208727 |
rs48165579 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91995964 | CTCTTAAACTATCTT[A/G]AACAAAATGCCAAAG | 208727 |
rs48170925 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92018158 | CTGTGACAGAGAGCA[C/T]AAAATATTGTGTTGA | 208727 |
rs48172479 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Hdac4 | GRCm38.p3 | 1:91990673 | ATGAGGAGGACTCAC[C/T]GGCCCTGTGCCTAGA | 208727 |
rs48190185 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:92017682 | GCCTGTACTGTCCAG[G/T]GAGAAGACACCACTG | 208727 |
rs48192072 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92039773 | TGTATGAAGGACTTA[C/T]AGTGGAAAAGTCAAA | 208727 |
rs48198182 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92050321 | TATCTTAACAAAGGT[C/T]TACTGAAAAACTCAT | 208727 |
rs48204780 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92018991 | CATGATAGATGGTCC[A/C]CACACAGGTTTTTTT | 208727 |
rs48207533 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hdac4 | GRCm38.p3 | 1:91937821 | CCAAAGAACGGGACG[A/G]ATGATACTCTAAAGA | 208727 |
rs48214552 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92023871 | CAAAAAGATATTATG[C/T]CCCAGATTAAACATT | 208727 |
rs48220279 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91974630 | CAGAAGCTAAATCTA[C/G]AGTGTCATTGGACTG | 208727 |
rs48242961 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92040547 | GAGATCCAGAACTCA[C/T]AGCTCAGCCAGCGCA | 208727 |
rs48245026 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91943596 | TGCAAGAGTCTTCCA[C/T]TGAGCCACTGACACC | 208727 |
rs48247881 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91934773 | TCTACTAGAGACAGC[A/G]CCTCACTCCCAAAGA | 208727 |
rs48250303 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91985709 | GATAATCATGCTAGC[C/T]GTTATTTCTGTTTAT | 208727 |
rs48252004 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92015308 | CCTGACACACACATT[G/T]CAAGGTTCATGCTTC | 208727 |
rs48253272 | snp | A/T | 0.18 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92043933 | ATATGAATAAGCATA[A/T]TTTCCCTAATATCCT | 208727 |
rs48264474 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:91957059 | TCTGTGCTCAGTGCA[C/G]ACTGTGGATGGATGC | 208727 |
rs48273747 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91952770 | GTAGTCACAAGGGCT[A/G]TGTGTAATCTTACTA | 208727 |
rs48275697 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92028151 | AATAATAGTGAGAAG[A/G]GGCCATGATGACACT | 208727 |
rs48276745 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91959194 | CACTTGAACCACCTC[A/T]GATACACCCACTGGG | 208727 |
rs48280860 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92055520 | ACCACCAACACTTGG[A/C]ACTGGATGGATAAAA | 208727 |
rs48281143 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91940676 | TCACAAAGCAAGTGC[C/T]GCAGACAGTGGGGGA | 208727 |
rs48281517 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92001490 | ATTCAGTAACTGGAT[C/T]GTAAAGATGTTGTCA | 208727 |
rs48295466 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91993761 | AACTGTAAGCTTGAC[A/G]TTCAGCAGCATGCAG | 208727 |
rs48298183 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | GRCm38.p3 | 1:91964016 | TTTGCTAGGACAAGT[G/T]TGGCCATGTGTTGGC | 208727 |
rs48304097 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92049539 | TCACAAGTGTAGAAT[C/T]ACCCGAGAATAGCAC | 208727 |
rs48315132 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Hdac4 | Mm_Celera | 1:91972812 | GCCAAATGACACAGG[A/G]ATGCCAGCAGCCTCC | 208727 |
rs48327426 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92065671 | AGTCATCAAGAAGCT[A/G]GAAGGGTACTCTCTG | 208727 |
rs48330529 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Hdac4 | GRCm38.p3 | 1:91989950 | ACCTGAGTAGCACAG[C/T]CTGGCTCCCAATTTC | 208727 |
rs48331086 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91965720 | TACTGCTTATGTGGT[A/G]GCCAGGGCTATGGAA | 208727 |
rs48332307 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91995761 | GAAGCTGTCACTAGT[A/C]CTAGAACTAACCTAC | 208727 |
rs48335588 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91988522 | CACTCATGCACCCAG[C/T]TAACAGGGCTCCTCA | 208727 |
rs48337004 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91975842 | GGAAATGATGCTCAG[A/G]ACTAAGGTAATGTGG | 208727 |
rs48339381 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91945254 | ACCTGAAGCTCATTC[C/T]AACTGGGTCTCTGTT | 208727 |
rs48350641 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91969964 | CCAGAGTGACAACCC[A/T]ATGTCTGCCACACAG | 208727 |
rs48362235 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Hdac4 | GRCm38.p3 | 1:92028081 | AGGCTTGTCCAGAGA[C/T]GCAATGCAGCATCAA | 208727 |
rs48390849 | snp | C/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91941155 | ACATCCCTTCTGGAT[C/G]CTGGAATTTCAGGAT | 208727 |
rs48394267 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91953469 | TGAAGCTTTAGAAGG[A/C]GCTCTCAATAAGGGG | 208727 |
rs48408083 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91990443 | GTAATGCTTCTTGGG[C/T]TTCCCTAGATGTTTC | 208727 |
rs48411082 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92028974 | TAAGACTGGTCTAGT[G/T]ACGGCAGCATTGTGG | 208727 |
rs48424185 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91966570 | GCAGTGTCAATGTGC[A/G]AAGCTTAGCAGGAAG | 208727 |
rs48427199 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Hdac4 | GRCm38.p3 | 1:92023412 | CACCTTGCTCTCCAC[A/G]GCCACACAACCAAGT | 208727 |
rs48433378 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Hdac4 | Mm_Celera | 1:92022134 | TCATCCTTCTAGACA[C/G]ACTCAGCAGTGAGCC | 208727 |
rs48440564 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92014914 | ACTAAAGCAAAGAGG[C/T]AGCCTAATAAAGTTT | 208727 |
rs48447165 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91952748 | ACAGGTGGTACCAGC[A/G]GAGTGTGTAGTCACA | 208727 |
rs48449486 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | Mm_Celera | 1:91997627 | GGCTGTAAATGAGCT[A/G]GAACAAGAGGCTACT | 208727 |
rs48454217 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91978047 | TCCACTAACAACTTC[G/T]GTGATCCTTTCTGGC | 208727 |
rs48459947 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92043542 | CAAATGCTGTGGCTA[G/T]GCAGTGGCTCAAGGG | 208727 |
rs48472538 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92022464 | TAGCTCTTCTAAGCT[A/T]CATCCCATCTATCAA | 208727 |
rs48482548 | snp | A/T | 0.244898 | 0.249948 | synonymous-codon | Hdac4 | Mm_Celera | 1:91956156 | CCCATTCCCATGATG[A/T]ACATCCTAAGAGAAC | 208727 |
rs48492267 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92017546 | TTCCTCAGCCCATTA[C/G]CACAGAACACTGTCA | 208727 |
rs48492547 | snp | A/C/G | 0.5 | 0 | intron-variant | Hdac4 | GRCm38.p3 | 1:92004108 | GGACTTGGAGGGATC[A/C/G]TGAATTCATGGAACT | 208727 |
rs48492889 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92045170 | ACAGATGCTAGAGCT[C/T]TGAACTGGATCTGAG | 208727 |
rs48496695 | snp | C/T | | | intron-variant | Hdac4 | Mm_Celera | 1:92011884 | GGAACCTTTAGGAGG[C/T]GCAGCCTTGCTAGAG | 208727 |
rs48510220 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91993901 | AGCGGAGGGTAAGTG[C/T]GTCTCCTAAGCCATG | 208727 |
rs48510963 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91953707 | CCAGTCACTCAGCTG[C/T]AAGGACTGATGAGTG | 208727 |
rs48512739 | snp | A/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91956703 | AAGATTGAGAACGAC[A/T]GACATAGGATATGTG | 208727 |
rs48529274 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91962808 | AGTGTCTGTAACCTG[A/G]CCAAGCTCCTTTCTG | 208727 |
rs48545844 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91936907 | AAGGGAAATGGAGGG[C/T]AGTGGGTTGATATTG | 208727 |
rs48557864 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91945858 | TGCAGCGGCCTGGTG[C/G]CTGTGGTGAGCACAC | 208727 |
rs48560618 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91948641 | CCCAGAAGACAACTG[A/T]GTCTCATACCCTTTC | 208727 |
rs48566220 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:92042842 | AATGTTAAGCCAGTA[C/T]ACTGGACCTGATGAG | 208727 |
rs48573864 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92040271 | GCTCTAAGCTGGAAG[C/T]CAGAAATCTGCACAT | 208727 |
rs48577830 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91961752 | TGACAGTGAGCATCC[A/T]AACCTACTGACTCCC | 208727 |
rs48581705 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:92010925 | CACTTCTAGTTTGTG[G/T]TAACTGAAGCAATGA | 208727 |
rs48584173 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92031116 | ATCATAGCATGCATC[A/G]CCTACTTACCACCCA | 208727 |
rs48634581 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91938366 | ATGTGTGTAATAGCG[C/T]GTGCTCACAAAGTTC | 208727 |
rs48654741 | snp | A/C | | | intron-variant | Hdac4 | GRCm38.p3 | 1:92023411 | TCACCTTGCTCTCCA[A/C]AGCCACACAACCAAG | 208727 |
rs48685321 | snp | G/T | | | intron-variant | Hdac4 | Mm_Celera | 1:92142367 | CCAGTGCAGGCCTTC[G/T]GGGGGGACATCTCCA | 208727 |
rs48706260 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92013573 | CTAACGGCATGAAAG[C/T]ATAAAGTCCTTGTAA | 208727 |
rs48710451 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91951340 | TACTCTAACTTACTC[C/T]GGGCTGATGGCTGCC | 208727 |
rs48710590 | snp | A/C | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91937679 | AGCCAACAACAAAAA[A/C]ACGAGTCGCTGGGCA | 208727 |
rs48712014 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:92051783 | CATCACATGCATGCA[G/T]TCTCAGAACACTGGG | 208727 |
rs48726720 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91937080 | ATATTCTTGAGACCC[G/T]GTAAGAATGTCCTGC | 208727 |
rs48735702 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92004028 | GATCTACAGACCCTA[A/G]ACAGCAAACCACCAC | 208727 |
rs48737719 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91992119 | TTCTGTGAAGGGCAA[C/T]TGATGCTCCAAAAAC | 208727 |
rs48740861 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92054812 | AAATGCCATTCGGCT[C/T]TTGTCACACTGACTT | 208727 |
rs48747067 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91948375 | AGGGCCACAAACAGT[C/T]CGGCCTCATTAGATG | 208727 |
rs48757943 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91969268 | GGTGCCTGTGGCCTC[A/G]CCGCACCCCTGTTCA | 208727 |
rs48761337 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92065303 | GGTCTAGTAAATGGA[A/C]TGTGTGGTATGAGAG | 208727 |
rs48761906 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91972892 | GGAGGGCTTGCTGCA[A/G]GGCAGGAAAGAGGGC | 208727 |
rs48767032 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92029893 | TCACATGTCTAAGCT[C/T]TCCGGAGATAAACAG | 208727 |
rs48771322 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hdac4 | Mm_Celera | 1:91992711 | CAAGCTTGGGCAACA[C/T]GTTCATTTGTGAGGC | 208727 |
rs48781926 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92044932 | TCATTCTGAGGACAA[C/T]AGGAAAATGTATCCT | 208727 |
rs48796895 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91950333 | TGTCTCGAGCATCCA[C/T]TTGTGACACCATAGG | 208727 |
rs48800071 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91965816 | GTCATGTTCATAATC[C/G]AGCCAGCAAAAAAGG | 208727 |
rs48814185 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92067347 | TTTTTAAATGTTACA[A/G]AGCTTTCCTTAATTT | 208727 |
rs48821524 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91949872 | CAGAACTCCTGTCTT[C/G]AAAATAATAGAACCT | 208727 |
rs48826434 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91948530 | GGTTGTGTTGTCTGG[C/T]CATGTGACTGCACAG | 208727 |
rs48862398 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91957189 | GTAAATGAATCATAG[C/T]AGTATCTATGTGTGT | 208727 |
rs48865038 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92055840 | TCAACTCTGAAGACA[A/G]AAGCCTCAAGCCAGG | 208727 |
rs48873067 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:91939136 | TGGGAATGTGGGAAC[A/C]GGGAAGGAACTCCAC | 208727 |
rs48877075 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | GRCm38.p3 | 1:91936408 | GGCAAGGCTGGCTGG[C/G]AAGAAAAGGTTTCTG | 208727 |
rs48894575 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Hdac4 | Mm_Celera | 1:91968387 | GAGAGGATTTGTGCC[A/G]TAGAGGAGTGTGTGG | 208727 |
rs48916313 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:91943087 | GCTAGCTCAGTAGTG[C/T]TAGCTTCCTGCTGAT | 208727 |
rs48924746 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91967133 | GGGTCAGTAGCAGAC[A/G]GCACCTGGACCACAC | 208727 |
rs48928361 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92005692 | ACACTGGTCTAGATC[C/T]CAGCACTGGCTGCAC | 208727 |
rs48934844 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91982561 | ATCAGCTTGCCACAC[A/C]TCCAATAGACGTTTC | 208727 |
rs48940685 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91988133 | GTAGCATTCAGGAAA[C/T]AGGCAGTGGCTTCTG | 208727 |
rs48993788 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91945364 | GCTCACTGTACTTTA[A/G]CCCTCAAAAACTTTA | 208727 |
rs48999395 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91992775 | GGAGAAGTTCCCTAC[C/T]TCCATGTGGCATTAC | 208727 |
rs49000543 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hdac4 | Mm_Celera | 1:91946895 | GGTGACAGCCAGCCA[C/G]GTCACTGTGTGACCC | 208727 |
rs49003561 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91975326 | CGTGTACCTGAGAGT[A/G]TACAACAAACCCAGC | 208727 |
rs49008267 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92021308 | GCCACCCTGTTGATG[A/G]GAGCTCCCAGGAAGA | 208727 |
rs49044095 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:91991946 | ACAATTCATCTGTAA[C/T]TTTAGAGTAGTGATG | 208727 |
rs49051901 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92065115 | AACTTCCCATGCAGC[A/G]TTTAGCTTACTGATC | 208727 |
rs49054589 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91943335 | CTTCTTGCCTTCTTC[A/C]GTGTGAAACAATCAG | 208727 |
rs49060583 | snp | A/G | | | intron-variant | Hdac4 | GRCm38.p3 | 1:92018110 | GCCATGATGGTCGTG[A/G]GCTCACCCTTTGAAA | 208727 |
rs49068900 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hdac4 | GRCm38.p3 | 1:92017480 | GTCCTGTGTGTGTCA[C/T]GACATCTTGAGGTCA | 208727 |
rs49096249 | snp | A/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91948982 | GCAGAGTAAAGTGGT[A/G]TGGTGTGGCCTTACA | 208727 |
rs49097698 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:91956335 | GCACATAGTGTAGTC[C/T]TGACTTCAGTGAAAG | 208727 |
rs49112843 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hdac4 | GRCm38.p3 | 1:91937946 | TTACTTGGTGGATAC[A/G]TGCGATTCCAAAAAC | 208727 |
rs49124781 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91952524 | GAGGTTGCTGATTCA[C/T]TGGACTTCCTTTGTG | 208727 |
rs49136910 | snp | A/G | | | intron-variant | Hdac4 | Mm_Celera | 1:92038846 | CACATGCCAGCTACA[A/G]AAACTGGCTACCTGC | 208727 |
rs49141548 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92063970 | CAGCAGCTCTCAATA[C/T]AGGCACCTTCAGTCA | 208727 |
rs49143736 | snp | A/G | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91953702 | CCGGCCCAGTCACTC[A/G]GCTGTAAGGACTGAT | 208727 |
rs49146327 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91939025 | ACGGTGAGTTGCACT[A/C]CAGGCACGGGGTCAA | 208727 |
rs49151208 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92027898 | CACTAGTATCACCCA[A/G]AAGCCTGGAATTAAC | 208727 |
rs49158170 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91971689 | ACATGAACACAGCCT[A/G]TAGCTTTGGACTGTA | 208727 |
rs49175308 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:91949354 | CCCTGAGGTGTTTAA[A/G]CAGCAACCACAGATA | 208727 |
rs49188855 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91938061 | CCGTTAGGTAACAGA[A/G]ACCTTGAATGTTCAT | 208727 |
rs49201481 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92043285 | AGAAGCAAATTCTGT[A/T]AGGTAGTATGACCAA | 208727 |
rs49216772 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91990145 | CCTTGGGTCATGCTT[C/T]ACTCAGAAAGCAGAG | 208727 |
rs49222229 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91944590 | TAAGAGCCATCTAGT[C/G]CCTGGCCTACATGGT | 208727 |
rs49233133 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91948751 | CGACTACCATGCACT[C/T]AACTGCCAAAACAAT | 208727 |
rs49235215 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | GRCm38.p3 | 1:92062721 | ACTGTATGAATCTCC[C/T]GTTCCTTTTACATGT | 208727 |
rs49253728 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92057033 | CTGTAGAGAATGGGG[A/G]AACTTCAGGCCTAAA | 208727 |
rs49285845 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91969187 | AGGAGATTTTTCTCA[C/T]GACTTGTGTACACTG | 208727 |
rs49291193 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92059333 | GTAGTTAGTGAGATC[C/T]GAAACCCTTTCTACT | 208727 |
rs49303275 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:91951527 | CCTGGGCTGGCAGCC[C/T]GTTATTAGAGAGCTT | 208727 |
rs49303942 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92022061 | AACCACTTCTATCTC[C/T]ACTGGACCAACTGGC | 208727 |
rs49306193 | snp | C/G | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91999702 | TGACACTGATGAAGA[C/G]ATGCTACAAGTTCTT | 208727 |
rs49337545 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91934050 | GACACATGGAGACTT[A/G]CTGGCATCCAGACTT | 208727 |
rs49339916 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hdac4 | GRCm38.p3 | 1:92035159 | CATCACTCCCAGAGC[A/C]CGAGCACCACAGAGC | 208727 |
rs49343618 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Hdac4 | Mm_Celera | 1:92030806 | TGGCGGGCAGCATGA[A/G]CGTTCATCAGCGTGG | 208727 |
rs49345898 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91972570 | GAGTGGTTCTCAGGC[A/C]TGGCATGGTGCTGGC | 208727 |
rs49349934 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92003700 | TTGGGAGTGAGGAAC[A/G]GAGACTCTTGGTGAG | 208727 |
rs49351065 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:91937243 | TTGGGACTAGGCTGC[C/T]AGTTTGTCAGAGAAA | 208727 |
rs49351102 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92020794 | GCTGTTCCCAACACA[A/G]TATTTTATGTTCCCT | 208727 |
rs49368614 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hdac4 | Mm_Celera | 1:91957688 | TTTTCATGTAACATA[C/T]AATTCTGTAGAACAG | 208727 |
rs49379051 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91976458 | CCTGTATCTTAAGCA[C/T]GCTGAGTACGAACAT | 208727 |
rs49400764 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92024549 | TTATACACATTAGGA[G/T]GCATCTGAGAGGTGG | 208727 |
rs49407015 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91943295 | TCAAACTTCCTTCAC[C/T]ACGTGGTCACAGCTC | 208727 |
rs49407351 | snp | G/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:91966759 | AGCGGTGCTGGCCAT[G/T]AGCTGAGGAGCAGTG | 208727 |
rs49421583 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:91935956 | GATAGGAGGATTTGT[C/T]TGGCTCCGAGCTTGA | 208727 |
rs49421819 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92028489 | AGAGCACTGGGCAAT[G/T]ATCAGCAAGGCAATT | 208727 |
rs49425052 | snp | C/T | | | intron-variant | Hdac4 | GRCm38.p3 | 1:92016495 | CTATCCTCACAGAAG[C/T]ACCACACACTTTGCT | 208727 |
rs49426070 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92023084 | GGTAAGATCTAGAAG[C/G]ACTAGGAAACAACCC | 208727 |
rs49427056 | snp | C/T | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Hdac4 | GRCm38.p3 | 1:92031114 | GTATCATAGCATGCA[C/T]CGCCTACTTACCACC | 208727 |
rs49453762 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:92056329 | TAGAAAGCAGTAAAA[C/T]GCTCCAAAGGGTAGG | 208727 |
rs49518963 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:91967553 | GACCAGGCTACACCA[C/T]AGAAGGGCTCTGTGT | 208727 |
rs49519181 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Hdac4 | GRCm38.p3 | 1:91953835 | TCAGAAATAAAGGCC[A/G]CTTACTGGGCAATGA | 208727 |
rs49540454 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91944429 | GAAACTTGCAGAGCA[C/T]ACCACACAGAACATG | 208727 |
rs49543895 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92052778 | AAGGCAGAGTCCAGA[C/T]AGACAGACAATGCCT | 208727 |
rs49564122 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac4 | GRCm38.p3 | 1:92021951 | ATACAAACAGAGTCT[A/G]AGCATGGACCTGCTG | 208727 |
rs49564920 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:92037676 | TGAGGAGCAGCTCAG[A/G]TATTTCAAGAGTAGT | 208727 |
rs49584327 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Hdac4 | GRCm38.p3 | 1:92016390 | TGGCCTCTAAAGTGG[A/C]TCTCTGCCCTGAGCT | 208727 |
rs49584354 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Hdac4 | GRCm38.p3 | 1:91937263 | TGTCAGAGAAACATG[C/T]AGGACCTAGTTAAGT | 208727 |
rs49598357 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hdac4 | Mm_Celera | 1:91963484 | GGCTGTAGCAGAGAC[A/C]CAAAGAGACACTAAG | 208727 |
rs49638069 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hdac4 | Mm_Celera | 1:91962201 | AGCTTCACTCTCAGA[A/G]ATAGATGATTTAAAC | 208727 |
rs49652576 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hdac4 | Mm_Celera | 1:92013811 | AGCTTGCCTCCAGCT[C/T]GAGCATGTAACCTCG | 208727 |
rs49662717 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, upstream-variant-2KB | Hdac4 | GRCm38.p3 | 1:92030132 | TGAGAACTGGTGGTC[C/T]AAGCGCAGGTCCATG | 208727 |
rs49681317 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac4 | Mm_Celera | 1:92040526 | GAGGAAGATGCACAG[C/T]CCAGGGAGATCCAGA | 208727 |
rs49685029 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Hdac4 | GRCm38.p3 | 1:92015910 | AGTCTAGCTTCCCTA[A/T]TGCTATAGAAGTAAG | 208727 |
rs49690202 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac4 | Mm_Celera | 1:91944447 | CACACAGAACATGCA[C/T]TTAACTTTGAGTCTG | 208727 |