SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3024157 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | GRCm38.p3 | 19:14456802 | GCTCCAGGTCCTCCT[C/T]ATTTGACTCAGAGAA | 21888 |
rs3024158 | snp | G/T | | | intron-variant | Tle4 | GRCm38.p3 | 19:14456764 | TATTCACTTCCCAGC[G/T]TCTCCACCCTTTCCT | 21888 |
rs3024159 | snp | G/T | | | intron-variant | Tle4 | GRCm38.p3 | 19:14456713 | CAGTGCTGGGCTGCT[G/T]TTTGTAAACATGACC | 21888 |
rs3024160 | snp | A/G | | | intron-variant | Tle4 | GRCm38.p3 | 19:14456705 | GGCTGCTTTTTGTAA[A/G]CATGACCAGCTTAGA | 21888 |
rs4232065 | snp | G/T | 0.21875 | 0.248039 | utr-variant-3-prime | Tle4 | Mm_Celera | 19:14449501 | AGATTCCATTCACTG[G/T]TAGGTATTCCATGTT | 21888 |
rs4232066 | snp | A/T | 0.244898 | 0.249948 | utr-variant-3-prime | Tle4 | Mm_Celera | 19:14449525 | CCATGTTCTTCCAAG[A/T]CGATAGCTGAAGATT | 21888 |
rs4232067 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Tle4 | Mm_Celera | 19:14449603 | GAAGTGGGGCTATGG[A/G]AAGGGATTAAACTCC | 21888 |
rs4232068 | snp | A/T | 0.21875 | 0.248039 | utr-variant-3-prime | Tle4 | Mm_Celera | 19:14449631 | TCCACAACTGCAATG[A/T]GTATTGGAAATCCTT | 21888 |
rs6209538 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552231 | GATGAAAACACATGG[C/T]CAGGTGAAGCAAGAC | 21888 |
rs6210077 | snp | A/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14552353 | CCTGCATATACCTAA[A/T]TGTNAAATTCACAAA | 21888 |
rs6210091 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Tle4 | Mm_Celera | 19:14552357 | CATATACCTAANTGT[A/T]AAATTCACAAATTGG | 21888 |
rs6210643 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552457 | ACTGGAACCCATTTC[C/G]GAAACTGACAAACTG | 21888 |
rs6211156 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552542 | CTCCTAGTTTGAGCA[A/G]TTCAGCCAAGCCCAC | 21888 |
rs6211167 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14586072 | GACACTGAGGGTGGC[A/G]GGAAGGGGAACAGTT | 21888 |
rs6211261 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14552610 | TAAAACGTAAAGAAG[C/G]AATATGAGCAATTAG | 21888 |
rs6211696 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552651 | TTACAGACCAATAAC[A/T]CTGCTACCAGTGCAT | 21888 |
rs6296654 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14596926 | GCCCGCGGTCCGAGA[C/G]GTGGGGGGGTTGGTC | 21888 |
rs6306622 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552088 | TACAAGGCTGTCAAT[G/T]CGGCCTTTGGAGGGA | 21888 |
rs6307035 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552128 | TTAATTAAACCTGCA[A/G]GAGAAACAGAAAATG | 21888 |
rs6307076 | snp | C/T | 0.49926 | 0.0192165 | intron-variant | Tle4 | Mm_Celera | 19:14552147 | AAACAGAAAATGACC[C/T]CCTGAGAGTTATCTT | 21888 |
rs6307159 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Tle4 | Mm_Celera | 19:14552191 | TCAAACAGATCATAC[G/T]GCTACCATTATGCCA | 21888 |
rs6332026 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Tle4 | Mm_Celera | 19:14598820 | AGAGGGAGGATCGCG[C/T]TGATCCCACTCCGTG | 21888 |
rs6333703 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Tle4 | Mm_Celera | 19:14599169 | AAGGAACCTCTGACC[C/T]CTGGGCAATCAAAAG | 21888 |
rs6341573 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Tle4 | Mm_Celera | 19:14481926 | GACAAACCAGTAAGG[A/G]ATAAGCATTCTGAGT | 21888 |
rs6341596 | snp | G/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14481942 | ATAAGCATTCTGAGT[G/T]CTCCGTACTGGCTCT | 21888 |
rs6341625 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Tle4 | Mm_Celera | 19:14481958 | CTCCGTACTGGCTCT[G/T]AGCCATTGGAGCACA | 21888 |
rs6341678 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14481993 | AAGAGACTACGAGGG[A/G]ACAggagggagggag | 21888 |
rs6342134 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14482045 | aggcagggaAATGGG[C/G]TGTGTTGTGGTGGGG | 21888 |
rs6342178 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Tle4 | Mm_Celera | 19:14482075 | GATGACACCCTGGCC[C/G]TATCCCAGAGCAATT | 21888 |
rs6371376 | snp | G/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14561230 | GAAACAGCCAAAAAG[G/T]GGGGGAGGGGGGCAC | 21888 |
rs6371918 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Tle4 | Mm_Celera | 19:14561347 | ATAGTTACTCTGTTA[C/T]TTACTTTTGGCAGCA | 21888 |
rs6372493 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Tle4 | Mm_Celera | 19:14561487 | AATTTTAAAACTGTA[C/T]ATCAACCTTAAGTAT | 21888 |
rs30304570 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14589532 | AACAAAAAAACACAC[A/G]AACAAACATGAGCCC | 21888 |
rs30307764 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14498945 | CATGTTCCCCCCCCC[A/C]CCCACACACACACAT | 21888 |
rs30312892 | snp | A/C | 0.42 | 0.183303 | intron-variant | Tle4 | GRCm38.p3 | 19:14481680 | TTTTTTTTAGACAAT[A/C]GAAAAATGATGGTAA | 21888 |
rs30315772 | snp | G/T | 0.375 | 0.216506 | intron-variant | Tle4, Gm31441 | GRCm38.p3 | 19:14566074 | ATGGAGAGGTGGGGA[G/T]AGAAATAAAAGATAA | 21888 |
rs30319902 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Tle4 | Mm_Celera | 19:14584747 | CTTTCTGTGCGGAGT[A/C]TAGTTCAGGAACAGA | 21888 |
rs30321729 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14457793 | AACATCCCCCACACT[A/G]ATACTAGCACTATTG | 21888 |
rs30322732 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Tle4 | GRCm38.p3 | 19:14554755 | CTCTAAGCTGTAACT[A/G]ATTTGTACCAGAAAG | 21888 |
rs30322734 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14465782 | TCAGGATACACCCAC[A/G]CAGGAATCACCATAG | 21888 |
rs30323350 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Tle4 | GRCm38.p3 | 19:14549123 | CAGTTCCAGTGGATC[C/T]AATACCCTTTTCTGA | 21888 |
rs30324508 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14543954 | ATTTTAATGAAAGTA[A/G]ATGGAATAATTAGCA | 21888 |
rs30325400 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14482558 | AGAATTTAAGCAAAC[A/T]GTGGTAAAAGCCAAG | 21888 |
rs30349940 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14583508 | GAATACTGGCTGCTC[C/T]TCCTGAGGACCCAGA | 21888 |
rs30354443 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14545183 | ACTCATCCCCTGTTC[A/C]TTTCTGCAGCTCCCT | 21888 |
rs30354691 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14581483 | CTACTTAGAAAACTC[G/T]GGATTTTATTGTATT | 21888 |
rs30355293 | snp | A/C | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14502174 | ACATATATATATTCC[A/C]CCCCCCCCCCCCATT | 21888 |
rs30355853 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Tle4 | Mm_Celera | 19:14455891 | TACATTGATCAGACT[C/T]GAAAATCACAAATTC | 21888 |
rs30357574 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14581419 | GCTCCCTCCTTGCAG[A/G]TAACTCTATTTTGTG | 21888 |
rs30357760 | snp | G/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14596648 | TCTGCCCACAGGGGG[G/T]AAATGGTAATACCTT | 21888 |
rs30359646 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14500007 | TCCTTCCACTGCTTC[C/T]TCATTTACATCCTGA | 21888 |
rs30363015 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14555652 | AGTGGACAGCCCATG[C/G]TAAAAAATATATTTG | 21888 |
rs30364756 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14576343 | CCCCCCAGATTATCA[C/T]CAATCAGCAGGACAG | 21888 |
rs30367184 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14574837 | CACTGAACGACAAGC[A/G]AGCTTGTGGGAGAGC | 21888 |
rs30371814 | snp | C/T | 0.487535 | 0.077957 | intron-variant, upstream-variant-2KB | Tle4 | GRCm38.p3 | 19:14550107 | AAAACCAAATGCTGT[C/T]TGGGTTGGTATGGGA | 21888 |
rs30372504 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14453477 | AGACGGAGACAAACA[A/C]ACAAACATACGACAC | 21888 |
rs30372619 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14581481 | AGCTACTTAGAAAAC[C/T]CGGGATTTTATTGTA | 21888 |
rs30372695 | snp | G/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14458505 | ACACTCAAAGAGTCT[G/T]CCAGAATAGCCTTGA | 21888 |
rs30376763 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Tle4 | Mm_Celera | 19:14576218 | TTTAAGATGACAATT[A/T]AAAAAATCACTTTAT | 21888 |
rs30400476 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Tle4 | GRCm38.p3 | 19:14543289 | CACTGTGTACATTAT[A/G]CTCCATGAAGTGGCA | 21888 |
rs30402227 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14524255 | TAAAGGGAACTGCAA[C/T]CCTATAGGTGGAACA | 21888 |
rs30402881 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14572409 | ACAGAATGTAGATGC[A/G]ACATAAATACCTTTA | 21888 |
rs30406075 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tle4 | GRCm38.p3 | 19:14578564 | CAAATTTAACTCAAG[C/T]TTCATGTTTACTATG | 21888 |
rs30408567 | snp | A/T | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14524248 | AAGTAGCTAAAGGGA[A/T]CTGCAACCCTATAGG | 21888 |
rs30409949 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14557949 | AGCTACTGTCCAAAC[A/G]CCTTTAATCCCAGCA | 21888 |
rs30410733 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Tle4 | GRCm38.p3 | 19:14569166 | TTAACCTGAGCTTTC[A/C]GAGTATAGGGTGGAA | 21888 |
rs30414690 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Tle4 | GRCm38.p3 | 19:14576379 | CAATTTTGGTCAGGA[G/T]GTAAATCAATTAGTT | 21888 |
rs30414754 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14574555 | ACAGCCTGTGTGTAA[A/T]GTGTGTTACTACTTA | 21888 |
rs30415478 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Tle4 | GRCm38.p3 | 19:14480910 | CTGAGCCCTACTCTG[C/T]GGCAGGCACTGTGCT | 21888 |
rs30417610 | snp | G/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14572658 | ACTACCTGGTATTCA[G/T]TCTCCAAGTATTTAT | 21888 |
rs30418421 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Tle4 | GRCm38.p3 | 19:14577985 | TCATTACTGTGTTTA[C/G]AGAAAGCACTCAGAA | 21888 |
rs30425446 | snp | C/G | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14461243 | GGGGGGGGGGGGGGC[C/G]CTATTGTGGGTGGTG | 21888 |
rs30426596 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Tle4 | GRCm38.p3 | 19:14582098 | TATTCAAAAAAGTCA[C/T]AATGCGCCCAAGCAT | 21888 |
rs30444659 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | GRCm38.p3 | 19:14532194 | ACTTCTAGATTCCAA[A/G]TTGTGTTTCATTATT | 21888 |
rs30446462 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Tle4 | GRCm38.p3 | 19:14536294 | ACACAAGAAATTATC[A/T]CAGAAAAGTGGAAGA | 21888 |
rs30447526 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14544329 | GTTCATCTACTATTT[A/G]TCCTAAAAATGGACA | 21888 |
rs30454034 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14574694 | CAAGCAGGAATAGCA[A/G]GGGGCAGATTGTAGA | 21888 |
rs30455881 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14555779 | AGAGATGATATATAA[A/G]GGGTATGATCAAAAC | 21888 |
rs30503305 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14457772 | TGCCACACCCTGTCA[C/T]CCTCCAACATCCCCC | 21888 |
rs30512691 | snp | A/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14462982 | TGTCTCGAAAAAACC[A/T]AAATAAATAAATAAA | 21888 |
rs30512798 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14558374 | CTCCTTGATAAGCTA[C/T]AGTACAGCAAAATTT | 21888 |
rs30515572 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14525433 | AATCTCAACAGCGAA[C/G]TTCTCAAACACTATG | 21888 |
rs30518577 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14473135 | GAACTGTCCCCAGGT[C/T]CACTGAAAGAACAGT | 21888 |
rs30520970 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Tle4 | GRCm38.p3 | 19:14574723 | GAAAACCTGTGGCCT[C/G]GATACATGGTGTGGC | 21888 |
rs30545330 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Tle4 | Mm_Celera | 19:14457573 | CACAAAGATTCCAAA[C/T]TGATAACACCTCAAG | 21888 |
rs30554390 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14525571 | GAGCAAGAAATCTAT[C/T]CAGACAAACTGTATC | 21888 |
rs30555350 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14561790 | GAACTCACACACACA[C/T]ACACACACACACACA | 21888 |
rs30555668 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Tle4 | Mm_Celera | 19:14581463 | CACTATGTTTTAGAC[C/T]TTAGCTACTTAGAAA | 21888 |
rs30563468 | snp | A/C | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14593683 | ACAAAAAACAAAAAA[A/C]AAAAAAAAAAAACAC | 21888 |
rs30564028 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Tle4 | GRCm38.p3 | 19:14480943 | GCCCAAGACAACAGG[A/G]AAAAGAACAGGCAAA | 21888 |
rs30566930 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14583145 | CACTTGGGAGGCAGA[C/G]GCAGGTGGATTTCTG | 21888 |
rs30612622 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14529525 | ATAGAACCAACAGAT[G/T]CTCATGATCCTGATA | 21888 |
rs30614512 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14556305 | TCTTTCCTGATTTGG[A/G]GGAGGAAAATATTTA | 21888 |
rs30617509 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Tle4 | GRCm38.p3 | 19:14572961 | ATCATCTCCCAATGC[A/G]GTTCCATATCACACC | 21888 |
rs30619490 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14519416 | CCCTCCGTTAACCTA[A/G]CCTCGCACTCCATGC | 21888 |
rs30648924 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Tle4 | GRCm38.p3 | 19:14589579 | CCCGCTGGAGTTTAC[A/G]TTTAAGCATCAGAAT | 21888 |
rs30651608 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14529026 | TCTGTAGATCAGGCT[A/G]GCCTCAAACTCAGAA | 21888 |
rs30652807 | snp | A/T | 0.42 | 0.183303 | intron-variant | Tle4 | GRCm38.p3 | 19:14500191 | AAGTAGTGGGAAAAG[A/T]GGAGGAGTGGTATCA | 21888 |
rs30661465 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14487233 | TATTCTTTGTGTTAT[C/T]TCAAACATGAGAGGT | 21888 |
rs30666833 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14589478 | TATCAGTAATCTTAC[A/G]TTATAAAATGCTGCT | 21888 |
rs30691766 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14547661 | TGAAACATTCACTGT[C/T]GAAGCACCTTTATGA | 21888 |
rs30692754 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14583390 | ACAAAAACAAAACAA[C/T]TGTATTTCTTTTTAC | 21888 |
rs30699669 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14529041 | AGCCTCAAACTCAGA[A/G]ATCCACCTGCCTCTG | 21888 |
rs30700300 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Tle4 | GRCm38.p3 | 19:14550168 | CACTAGTATATCCAC[C/T]ACTTTACTCCCCTCT | 21888 |
rs30705660 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14452694 | TGGTATCTGTCGCCT[G/T]TGCAGGGGGAAGGCC | 21888 |
rs30710905 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Tle4 | GRCm38.p3 | 19:14479567 | TAATAGGATCACTGT[C/T]CACTGATCTGCCATG | 21888 |
rs30713051 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14502172 | ACACATATATATATT[A/C/T]CCCCCCCCCCCCCCA | 21888 |
rs30713545 | snp | G/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14536634 | AGTTATTAGTAGAAA[G/T]AAGGAAGGGAGGAAG | 21888 |
rs30714054 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14586077 | TGAGGGTGGCGGGAA[A/G]GGGAACAGTTGAACT | 21888 |
rs30743760 | snp | A/C | 0.498615 | 0.0262793 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | GRCm38.p3 | 19:14565894 | TTTAAGAATGCTTAA[A/C]CCACCATGAAAGGCT | 21888 |
rs30744634 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Tle4 | Mm_Celera | 19:14527157 | TCTGCTTGAAAATTT[C/T]ATATTCCTCATCCAT | 21888 |
rs30785861 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Tle4 | GRCm38.p3 | 19:14526799 | GATACACTCTCACAC[A/G]GGCCAAAGGATATGT | 21888 |
rs30794454 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14582293 | ACTCAGCCACTGCAG[C/T]CTCAAGTATCACTGG | 21888 |
rs30797727 | snp | A/C | 0.42 | 0.183303 | intron-variant | Tle4 | GRCm38.p3 | 19:14571083 | GGAAGCCATGTCACT[A/C]AAAAAGCAACATATA | 21888 |
rs30799336 | snp | A/G | 0.432133 | 0.171253 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | GRCm38.p3 | 19:14565242 | TTTTTTGGAAATACA[A/G]GGACAATGCACATGA | 21888 |
rs30801939 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Tle4 | GRCm38.p3 | 19:14571795 | TTGAATACACTCTTA[C/T]TCAATATTTTAATAA | 21888 |
rs30814188 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Tle4 | GRCm38.p3 | 19:14496563 | ATGTCTTTTTGTGGA[A/G]AGACAAGAGAAGGTA | 21888 |
rs30820711 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14456391 | CAGTGGTGCTAATTA[G/T]GAGTTTTAGATGGTG | 21888 |
rs30846072 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14586078 | GAGGGTGGCGGGAAG[A/G]GGAACAGTTGAACTT | 21888 |
rs30849511 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14554416 | TTCAATATAGGAATG[A/G]ATACAGAAGATACTT | 21888 |
rs30850824 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Tle4 | GRCm38.p3 | 19:14574558 | GCCTGTGTGTAAAGT[A/G]TGTTACTACTTAATG | 21888 |
rs30858978 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Tle4 | GRCm38.p3 | 19:14575308 | TGGGACAGTATGGGG[A/C]CAATTCAGCCTCAGA | 21888 |
rs30863653 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14551827 | TACAATGTTCACACC[A/G]TTCCATTTGCACTAA | 21888 |
rs30900523 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Tle4 | Mm_Celera | 19:14569336 | AGTTACACATTCACA[C/T]ACCTAGGCACGGAGA | 21888 |
rs30943925 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14553406 | ATTGGGGTCCCCTTG[C/T]TCAGTCCAATGGTTG | 21888 |
rs30946728 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tle4 | Mm_Celera | 19:14544077 | AGAAGGAAAGGGGGT[C/T]TTCTTTGGAACGTGC | 21888 |
rs30950257 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14466101 | GAGACGGCGTAGGGA[A/G]AGATGCAGCTTGCTG | 21888 |
rs30951143 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14591579 | TTCCCACTGTGCCCT[A/G]GAACATTCCACTTGA | 21888 |
rs30955954 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Tle4 | GRCm38.p3 | 19:14460276 | CTAACACTGAAGTAA[C/T]AAAAAAGGAAGACAG | 21888 |
rs30957925 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14542564 | GAGGGAGAGAGAGAG[A/G]GAGAGAGAGAGAGGG | 21888 |
rs30961488 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Tle4 | GRCm38.p3 | 19:14555039 | GAGGTCCAGCCTACA[C/T]GATGCCTCCACCAGC | 21888 |
rs30963049 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB | Tle4 | GRCm38.p3 | 19:14598724 | CGACCGCGCGGGGGT[G/T]CGCACTAATTAGGGC | 21888 |
rs30963221 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Tle4 | GRCm38.p3 | 19:14458047 | GGAACATTGTAGACT[G/T]GACCCAATTGTGGTA | 21888 |
rs30980023 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14572338 | AAGGGTTTTGAAAAT[A/C]ACCCATATATCCTTT | 21888 |
rs30982014 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Tle4 | GRCm38.p3 | 19:14497872 | ATATAGTATTTACAT[C/T]ACATTACTTATTTTG | 21888 |
rs30982023 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14533213 | CAGGACAGCCAGGAG[C/T]GCACAGAGAAACCCT | 21888 |
rs31003298 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Tle4 | GRCm38.p3 | 19:14567589 | AGATATACATTTAAG[A/G]AAAGTAGTTGATGGG | 21888 |
rs31008160 | snp | C/G | 0.42 | 0.183303 | intron-variant | Tle4 | Mm_Celera | 19:14477351 | CCATCAAAACCCACA[C/G]ATGTTTATATTATGA | 21888 |
rs31014493 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14474138 | TGTGCAGAGAGGCTA[A/T]TGGGGCAATAGTATT | 21888 |
rs31018214 | snp | A/C/T | 0.495 | 0.0497494 | intron-variant | Tle4 | GRCm38.p3 | 19:14575478 | AACCTCAAATCAGAG[A/C/T]GCTGCCTCAGATATG | 21888 |
rs31028246 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Tle4 | GRCm38.p3 | 19:14582279 | AAGTGAGTGCTACAA[C/T]TCAGCCACTGCAGTC | 21888 |
rs31033954 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Tle4 | GRCm38.p3 | 19:14581568 | CTATTCTTCCGCAAG[A/C]TATGTCCTGATCCCT | 21888 |
rs31045956 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14529032 | GATCAGGCTAGCCTC[A/G]AACTCAGAAATCCAC | 21888 |
rs31046622 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14555827 | ATTATATTAAAAATC[A/G]TCACACAGCCGGGCA | 21888 |
rs31047664 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Tle4 | GRCm38.p3 | 19:14573720 | AACAATATGATTTCA[A/G]ATTTTGGCTATCGCC | 21888 |
rs31053386 | snp | A/C/G | 0.42 | 0.183303 | intron-variant | Tle4 | GRCm38.p3 | 19:14482920 | AGATGAGGCTTAGTG[A/C/G]AAGGTAATTAGGCAG | 21888 |
rs31053399 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14543599 | CCCCCCACCTAGCAT[A/G]AAGATGTGTGACAAA | 21888 |
rs31057399 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14524103 | ACTAGCAAGATTTTG[C/T]TGAAAGGACCCAGAT | 21888 |
rs31075381 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14560658 | ACACACACACACACA[C/T]ATATACATGACTCAA | 21888 |
rs31079785 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14590886 | AATAAAATTTTTGTT[A/G]CTTAAGGGCAAAAAA | 21888 |
rs31079791 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Tle4 | GRCm38.p3 | 19:14475799 | AGCAAAGATGCAGGG[A/G]TTTGAGTGTGTACAC | 21888 |
rs31086032 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14519718 | CATCTATCTCTCTCT[A/C]TATATATATAGTGCA | 21888 |
rs31086513 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Tle4 | GRCm38.p3 | 19:14571736 | AACTTGGGATTCTGT[C/T]TCTGGTACCCAAACA | 21888 |
rs31087182 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14543868 | GGACAATTGGCGTAA[C/G]TGAAGCAGGCGTCTT | 21888 |
rs31093799 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14583278 | CATACTATAGTAGAT[A/G]ATTCTAGATCATGAA | 21888 |
rs31093967 | snp | A/C/T | 0.456747 | 0.140554 | intron-variant | Tle4 | GRCm38.p3 | 19:14579103 | AATACACCTGTCAGT[A/C/T]ATCAGTTCTTCCCCA | 21888 |
rs31095549 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14529093 | AGGAGTGCGCCACCA[A/T]GCCTGGCTCCTGTAA | 21888 |
rs31103184 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14572462 | GAAGACAAAAAAAAA[C/T]CAAAAAAACATGTGC | 21888 |
rs31107499 | snp | A/C | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14583194 | TCTATAGAGTGAGTT[A/C]AAGGACAGCCAGGGC | 21888 |
rs31107644 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14456387 | CCAGCAGTGGTGCTA[A/G]TTAGGAGTTTTAGAT | 21888 |
rs31123916 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14497897 | ATTTTGTTTGTGGGC[A/G]TGTATGCATGTAGTG | 21888 |
rs31130541 | snp | A/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14550545 | AAATCCTACTTATCT[A/T]CTACAGAATTCTTAC | 21888 |
rs31134461 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14533476 | GCACTGACTGCTCTT[C/T]TGAAGGTCCCGAGTT | 21888 |
rs31136459 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Tle4 | GRCm38.p3 | 19:14479727 | CAAAACAGGTACTCA[C/T]GGACTTCTTCACACT | 21888 |
rs31137213 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14533067 | ATACTCAATTTCCCA[G/T]AGAAATTTTCCTATG | 21888 |
rs31138903 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14540328 | TCATCCCAATGCATT[C/T]GAAACATAAAATGGT | 21888 |
rs31139836 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14585108 | GAAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCG | 21888 |
rs31149744 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14473932 | TCCTGGGCACATCCC[C/T]AAAGGATGAAGTTCT | 21888 |
rs31150013 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14562005 | CCCTTCTCCATGCAA[A/G]AGTAGTTTTCCTGCT | 21888 |
rs31153701 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Tle4 | GRCm38.p3 | 19:14480748 | GGAGAATTCATGTTA[A/C]CTGTGCCTCTAGAAC | 21888 |
rs31176241 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Tle4 | GRCm38.p3 | 19:14582091 | ATCTCTTTATTCAAA[A/G]AAGTCATAATGCGCC | 21888 |
rs31187301 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14465455 | CAGCTATGAGAGCAT[A/G]ATTTTAAGAGTTACT | 21888 |
rs31188007 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14570712 | CTATCCACCCCCCAA[A/C]TACCCTCTCCCCTTC | 21888 |
rs31188080 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Tle4 | GRCm38.p3 | 19:14545823 | AAGAGGCATGTATGT[A/G]TTAGTTGATCTTTGG | 21888 |
rs31188217 | snp | C/G | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | GRCm38.p3 | 19:14562594 | ACCTTCTACTTCTGA[C/G]GATAATCCAGACTTT | 21888 |
rs31189675 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14532274 | AAAACATATATAAAT[A/G]CTTATTAGCATAGTG | 21888 |
rs31201797 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14583183 | GGCCAGCCTGGTCTA[C/T]AGAGTGAGTTAAAGG | 21888 |
rs31203489 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14456430 | CTGAAAGAAGCATGA[A/C]GGGCTTTGACATTAA | 21888 |
rs31205628 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Tle4 | GRCm38.p3 | 19:14481634 | CACACACATGCCAAA[C/T]TTGAAAAAAAAAATG | 21888 |
rs31206743 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14462340 | GTGTGAAAAACTTTT[A/G]GAGTGCTTGAGATGT | 21888 |
rs31238297 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Tle4 | GRCm38.p3 | 19:14525830 | ATTCACAGAGCATAA[A/T]CTGATCTAATCTAAT | 21888 |
rs31242354 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | GRCm38.p3 | 19:14595161 | GTGTCATTTCCTATC[C/T]GAATCATTAATTAAA | 21888 |
rs31245861 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Tle4 | GRCm38.p3 | 19:14531655 | AACAGATCATGCCAA[C/T]AATGCCTCTTTAACG | 21888 |
rs31255322 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Tle4 | Mm_Celera | 19:14598643 | GGCGATGGCGGTGAG[A/G]CTGCAGGCCGGTCCG | 21888 |
rs31267676 | snp | A/G | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Tle4 | GRCm38.p3 | 19:14548533 | ACAATACAACTTACT[A/G]ATAAACAGACCTTTA | 21888 |
rs31271838 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14561868 | TCATTTAATTTTTAA[A/T]TAAAAAACACTTAAA | 21888 |
rs31277441 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14533702 | AAAGGTTTGTATATT[C/T]AGCAAAGAAAATAAA | 21888 |
rs31282170 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | GRCm38.p3 | 19:14574681 | GAGAGAAAGAGAGCA[A/C]GCAGGAATAGCAAGG | 21888 |
rs31283705 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Tle4 | GRCm38.p3 | 19:14458393 | GGGTCACACCAGAGC[C/G]CGGACTGGGCTAAAT | 21888 |
rs31287739 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14504960 | GTCTGAAGAGCAAGA[C/G]AAGGTGTGTGCAGTG | 21888 |
rs31291825 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Tle4 | GRCm38.p3 | 19:14447720 | AAAATCTGTGAGGTC[C/T]AGTACAATAGCTGTT | 21888 |
rs31292255 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Tle4 | GRCm38.p3 | 19:14454076 | AAAGATCTAGTCTCA[C/T]TCCCACCACCAAATT | 21888 |
rs31298415 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14498538 | AGATCTTTGCTAGAA[C/T]AGTCCTGGCTCATGT | 21888 |
rs36240619 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14483073 | AGGATGACAAATAGA[C/T]CCACTCCACTTAAGG | 21888 |
rs36244167 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Tle4 | Mm_Celera | 19:14511284 | AGGAAAGTTGCTTTT[A/G]CAAGTGACACCTATA | 21888 |
rs36249815 | snp | G/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14465197 | GCTGCTCATTACTAC[G/T]TTTAACAGATTTTAT | 21888 |
rs36251952 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14495667 | ACACAAATTAAGAAC[C/T]TTAAAGAGGTTGTAG | 21888 |
rs36259502 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14481871 | GGTCTAGAATGAAAA[A/C]GGTTTTCTTTTGTTT | 21888 |
rs36260369 | snp | A/C | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14571138 | GAAAACTGCAAATTC[A/C]TTCTGGACAACCTCT | 21888 |
rs36262542 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14481497 | AATTCAGCCCAAATG[C/T]TTACAAATACCCTGA | 21888 |
rs36268153 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14455548 | GTAGGATAGCTAATG[A/T]CATATAATATATATA | 21888 |
rs36270530 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14517200 | AGTTAATCTCATGCT[C/T]TGAATAGCAGTAACT | 21888 |
rs36272629 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14459599 | CTTAGACCAAGGTGA[A/G]CACTGCTTATTAAAT | 21888 |
rs36279512 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14506014 | CCACCAAGGCAATAC[A/G]CATATAGCTTTGACC | 21888 |
rs36280974 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14578136 | TAAAGCTGTGCTAAC[A/G]TTAAAGAAAACATCT | 21888 |
rs36282204 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14561609 | AGTTTGGGAAAAAAT[A/G]ATAAACTATACACAA | 21888 |
rs36294365 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | Mm_Celera | 19:14562678 | CTGCTTAGGCCCAAG[A/C]CTAACAGCACCCCTA | 21888 |
rs36294743 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14450808 | CTTTCAGTTTGTATA[C/T]CTAAAAGGTCAAGTA | 21888 |
rs36294811 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14494680 | TCTGTCTAATGTTTT[C/T]TACTATACCACGGTT | 21888 |
rs36295971 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14479609 | ACCTTGGAGAAGTAA[A/T]CTGTTTCAGAAAATT | 21888 |
rs36297864 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14503188 | AAAGAACCTGGCAAA[A/T]AGGTTCCTGACTTGA | 21888 |
rs36299063 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14485609 | CATTACTATACACAC[A/G]CTCAAATCATACAGA | 21888 |
rs36300753 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14451348 | TGAAAACAGAAAATG[C/T]ATACATAAACACGAA | 21888 |
rs36301121 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14471234 | ATTTCCATAGCTTAC[C/T]ACCTAACGTACTTAC | 21888 |
rs36302380 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Tle4 | Mm_Celera | 19:14456153 | GGGGAAAACAGATCA[C/G]AATAGCAGGTAGGAA | 21888 |
rs36305055 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14521898 | AAACAAACTGAAAAA[C/G]GCTACCATAAACTCA | 21888 |
rs36308232 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14517748 | GGTAGATAACGCCAC[A/G]CTGATGCCCAAATGC | 21888 |
rs36310929 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14488498 | GGAGAGAGCTGGTCT[C/T]GCAGGAGTGCCTACA | 21888 |
rs36313896 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14450484 | GGCAGACATGAGCCA[A/C]AATGTCCACTGCTAC | 21888 |
rs36315515 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14579833 | GTTGATGCATCCAGG[A/T]CTGTAATAATTTCTT | 21888 |
rs36316279 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14496363 | TCTTTGGGAACGGAT[A/G]CAGAAACCATCCAAA | 21888 |
rs36318420 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14549675 | AAGCGGAGGCATGGA[A/G]ATACAGGAGTATGAC | 21888 |
rs36318779 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14495837 | TATGTGGTACTCAGA[C/T]ATGCATGCAGGTGAA | 21888 |
rs36322907 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14497205 | CAATCAAACATATAA[A/G]ATTGCAGCATCTATT | 21888 |
rs36323065 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Tle4 | GRCm38.p3 | 19:14530093 | GTATCTCTAAGTGAT[G/T]CTGCTTTGATGGTAA | 21888 |
rs36323542 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14516313 | GATTTATTCATATTA[C/T]TCATAATCCCTCTAC | 21888 |
rs36323775 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Tle4 | Mm_Celera | 19:14476908 | GACATAAAAATACCA[C/T]ATCAATATATAAGCA | 21888 |
rs36327255 | snp | C/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14574509 | CAAGGAATGCTGCAT[C/G]AGGTCACACCAACCA | 21888 |
rs36330863 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14481772 | TCAACGATAAGGTAA[C/G]GCACTCTAATGCTGA | 21888 |
rs36332222 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Tle4 | Mm_Celera | 19:14538986 | CTTTTAAACAATGGT[A/G]TTGCTGTTGAAGGAA | 21888 |
rs36334356 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14486266 | AGCGGCACACAGGAT[G/T]TAACAGACACATCAA | 21888 |
rs36334560 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14558368 | TATAAACTCCTTGAT[A/T]AGCTACAGTACAGCA | 21888 |
rs36335944 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14583885 | TGATTGCCTAGCAGA[A/G]GTCTTTTTGCTCATC | 21888 |
rs36336848 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14589929 | ACTTTTATCTACATA[C/T]TCAGACACATGCTTC | 21888 |
rs36337741 | snp | G/T | 0.444444 | 0.157135 | synonymous-codon | Tle4 | GRCm38.p3 | 19:14468155 | GGATGGACTTACATA[G/T]CGAGCTGCAATTTCT | 21888 |
rs36338886 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14483545 | TCTCTCAAGGAGACT[C/T]GATTACAGCGTGTAA | 21888 |
rs36340641 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14464287 | TTTTAGATAATGAAT[C/G]CAAAGGACAAAAGGT | 21888 |
rs36345942 | snp | G/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14457058 | CTTCAGGGGCTTCAC[G/T]AATAGTAGACACTAG | 21888 |
rs36346522 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14578400 | GGGTACTGTATGTGA[C/T]GCATGCTCCATATTG | 21888 |
rs36350693 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14501969 | TCAGCAGCATGCCTG[A/G]TAGGGAAGGTGAAAT | 21888 |
rs36351600 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14476907 | TGACATAAAAATACC[A/G]TATCAATATATAAGC | 21888 |
rs36357009 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | GRCm38.p3 | 19:14476928 | ATATATAAGCAATAT[A/G]AAATGTTTTGAGATA | 21888 |
rs36357255 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14497586 | ACTTGCCTGTCTCCC[A/G]AAATAAACATGACAA | 21888 |
rs36361066 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Tle4 | GRCm38.p3 | 19:14581516 | ACTGGGCAATAAACT[A/T]TGCTCCAAACAGAAC | 21888 |
rs36363377 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14551754 | CTTCACAAAAGTATT[A/C]GGAATTCCTATTTGT | 21888 |
rs36370970 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Tle4 | Mm_Celera | 19:14584130 | TCCTGGTGAGACGGA[A/C]GAGGCACAAAGGATC | 21888 |
rs36371770 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14460223 | GTGAAACAGGGAGAG[C/T]AAGAACACAAGGAGA | 21888 |
rs36374422 | snp | A/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14573694 | CAAAGCACCTCGAAC[A/T]TAGGAAATGCAACAA | 21888 |
rs36380743 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14579332 | GGTCTTTGCTCTTGG[A/C]CCCAGAGAAGAGTCT | 21888 |
rs36383652 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14587443 | AAACCTTACAAACTG[G/T]CATCAGTGTAAATCA | 21888 |
rs36384677 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14507883 | GCTTTTCAGGAACAT[C/T]TGATGAGTGCACAGG | 21888 |
rs36386125 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14453090 | AGCGCAAGCAACAAA[C/G]TACCAGGACTGGGTC | 21888 |
rs36386374 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Tle4 | Mm_Celera | 19:14451075 | TTAATCCACTCTATT[A/G]TGACTTGTCATTAAT | 21888 |
rs36387794 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14486259 | GGAAGACAGCGGCAC[A/G]CAGGATGTAACAGAC | 21888 |
rs36388677 | snp | C/T | 0.18 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14451135 | TGTGTTTGTGCTATG[C/T]TTAAATCTGGTAGGT | 21888 |
rs36388911 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14480414 | TAGTTCCACTGTTTA[A/T]ACTATCCAGTTTATG | 21888 |
rs36393283 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14498800 | TGTATCTGATAGATG[C/G]TCTCCCTCATTCTGT | 21888 |
rs36394096 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14463749 | TCTGAAGGTTTTCTT[A/G]TCCAATTTTCTAATC | 21888 |
rs36395575 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | Mm_Celera | 19:14563933 | AATTAATCAGGTAAT[A/G]AAAAATAACTTTCTC | 21888 |
rs36396153 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Tle4 | Mm_Celera | 19:14457899 | ATAGCTGCTAAACCA[A/T]ACCAATGTGGCAAGA | 21888 |
rs36396875 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Tle4 | Mm_Celera | 19:14543188 | TTTTCCTAGAAACAG[A/G]TGCTAATCAGATGCA | 21888 |
rs36397870 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14477188 | ATGTCTACTTTCCGT[A/G]ATTTTACCCGAAGTT | 21888 |
rs36400456 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14558549 | ATGTAATAGCAAAAA[A/C]AGCCATTATTTTCAT | 21888 |
rs36401354 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Tle4 | GRCm38.p3 | 19:14486602 | ACATGTTCTCTTACA[C/T]CCCAATGTTCTGGCA | 21888 |
rs36403413 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14555006 | GAGCCCAGACTACAA[A/G]TAATTTCATGTCAAT | 21888 |
rs36408247 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14493556 | GACTGAAGCCTGTGC[A/G]ATTCTTCTGTTTCTA | 21888 |
rs36409337 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14487313 | GTCAATGTTCCAATA[C/T]GACAGGAAACAGGGA | 21888 |
rs36410095 | snp | C/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14569836 | GCCACAGGCCACAAG[C/G]CACACATGTCCTAAG | 21888 |
rs36411198 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14571687 | AATAGCTTCGGTGTT[C/T]ATTGTTCCATCAGCC | 21888 |
rs36419347 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14486797 | CAGTATTCTGGCAAA[C/T]ACTCTTGAATTATGT | 21888 |
rs36419951 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14559473 | TCTGGTCCTGAGTCC[A/G]GATGAGCTCAGGTTC | 21888 |
rs36420491 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14525291 | CAAAGGTCCTCAACT[A/C]TTTGATCACCAGGAC | 21888 |
rs36423429 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tle4 | GRCm38.p3 | 19:14483245 | TTTGTTTTCTTAATA[C/T]CTAGTCTTGATGGGT | 21888 |
rs36423836 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14450384 | TAGGACATTCAAGAT[A/C]CAAGACCTCAGCTGC | 21888 |
rs36424494 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tle4 | Mm_Celera | 19:14451035 | CCACCAACCTTGTAT[C/T]GTGCTCTGTTTTGGA | 21888 |
rs36435816 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14458880 | GGGCAGCTGCCTCCA[C/T]AACGCTCATCTGAAG | 21888 |
rs36437032 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14584534 | CCAAACCGTCTACTA[A/G]TTAACTGTGGCGCTT | 21888 |
rs36439509 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14499648 | TGCTGTAAAACACAT[A/G]AAAGTCATGATCTCA | 21888 |
rs36440202 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14485987 | TAAGAGTGGCATATG[C/T]CCCATGTCTCAGCAA | 21888 |
rs36440307 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14503032 | AGTTTAAAAGTACTG[A/G]ATCCTGAAGATATCT | 21888 |
rs36441062 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14577970 | CTGAAAACAAACAGG[C/T]CATTACTGTGTTTAG | 21888 |
rs36441082 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14478684 | GGTGCATGAAGGAGT[A/T]GGAGGGAACGGACTT | 21888 |
rs36443265 | snp | C/T | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | Mm_Celera | 19:14564216 | TAAATTACATCACAG[C/T]AAACATTAATAAGGT | 21888 |
rs36446931 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14590470 | TTCGGCAGGTTTGCT[G/T]TATTTGCTCCATGAT | 21888 |
rs36449261 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | Mm_Celera | 19:14562856 | AAAATACAGACTAGC[A/G]AGAGGGCTGAATGGT | 21888 |
rs36452437 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14578913 | TAACTCTCTTGTGGT[C/T]TGGGTATATAATACA | 21888 |
rs36452765 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14571404 | AAATCAGTTTGGTTA[A/G]AATCAATCTTAGAAA | 21888 |
rs36454437 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14520164 | AGCTGGGGCCTATAG[A/C]TGCTTATATCTCTAA | 21888 |
rs36454492 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14507806 | TTCCCAGAACACTTA[A/C]GGATTTTTATGTCCA | 21888 |
rs36456406 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14578581 | TCATGTTTACTATGT[C/T]ACAACACAACAAAAG | 21888 |
rs36460888 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14570623 | TTATTTCAGGACTCT[C/T]TTCATTAATTTATTT | 21888 |
rs36467323 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14579699 | TCAAAAGAAAAGATG[G/T]TATTTTTTGAGGAGA | 21888 |
rs36468510 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14513374 | GGGATATAGAGACAG[A/T]AAGTAGTGAGAGCCT | 21888 |
rs36474335 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14457466 | AGAATTTAATCCTGA[A/G]TTCTAGGGTTGAAAG | 21888 |
rs36475117 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14508703 | AAGTGCCAAGCATAA[C/G]ACTTCAATCTTAGGC | 21888 |
rs36479085 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Tle4 | Mm_Celera | 19:14545623 | TAACACAGAAGTGCT[G/T]ACATGGGACATTTAC | 21888 |
rs36479714 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14458645 | TGCCAGTGAGGTGTT[A/G]ACACTGACAGTCACC | 21888 |
rs36483120 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14568514 | AATGGTATCACTACA[A/G]CAATGTTATCCTGGC | 21888 |
rs36487707 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14457552 | CTTAATAAAGGGACA[A/C]TGATCCACAAAGATT | 21888 |
rs36493758 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14514635 | ATTAGCCAACTATTT[A/C]AACTTGAAAACCTTA | 21888 |
rs36494510 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14484177 | AGCAAATAGCCATAA[A/G]AAGGAAACACTGGAA | 21888 |
rs36496850 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14510043 | AATACATCTGTTTCT[C/T]CATAATACTACAAAG | 21888 |
rs36501589 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14467981 | CAGATAATTGATGGC[A/G]ATAGCTTTGATACAC | 21888 |
rs36507934 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14568104 | CAGAACAGAGGATTC[A/G]CCTGTCAATAATGAA | 21888 |
rs36518404 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14498238 | AGAAACAAAATGGGT[A/G]CCTACTTCGATAACT | 21888 |
rs36521867 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14467749 | CGATTCAATTCACAT[C/G]GAGGACATCAATGCA | 21888 |
rs36523044 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14588275 | GAGCAGTGAGTAGGA[A/C]ATATGCCTTTGAATG | 21888 |
rs36529666 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14519511 | GGGAACAGCAGCCCT[G/T]ATTGGTCACGCAATA | 21888 |
rs36534130 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Tle4 | Mm_Celera | 19:14544532 | TTTAGCAATAGAAAC[A/T]AATGGCACAGTAAAG | 21888 |
rs36534688 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14574296 | AAAGTGAGCCTGAAA[G/T]ATGAAGATAGAAGGG | 21888 |
rs36537456 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14559901 | TTCTTCCTTGCCAAA[C/T]GTCTTAGGATTCAGA | 21888 |
rs36537716 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14569997 | CCTCTGTGCCTGTAT[C/T]CCTGAGTGTTTCTTT | 21888 |
rs36538184 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14501968 | GTCAGCAGCATGCCT[A/G]ATAGGGAAGGTGAAA | 21888 |
rs36538215 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14464967 | AAGCACACAGAAAAT[A/G]GTTGTTGCACCTTCT | 21888 |
rs36540170 | snp | A/C | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14557681 | AGATAGCACACAGAG[A/C]AAACTGTATTCCCAC | 21888 |
rs36541466 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14510300 | TCTGGCGTCCACACA[C/T]ATGCCATGGAACACA | 21888 |
rs36542707 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14568858 | CTTACGTAGTCACCT[A/G]TTACCATACTAGTTG | 21888 |
rs36544079 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14516530 | TTAATTATTAATACT[A/G]CTCTAACAAAATTCA | 21888 |
rs36545740 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14493974 | TATGTGATATTCGTT[C/T]TCATATATAATCTAA | 21888 |
rs36546065 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Tle4 | Mm_Celera | 19:14526655 | TAAAGACAAGAAGAA[A/T]AGAGAGAGATGGAGA | 21888 |
rs36546249 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Tle4 | Mm_Celera | 19:14525677 | AGTGTTTATTGTTTG[C/T]TTAATCTTCACAAAT | 21888 |
rs36546418 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14571750 | TCTCTGGTACCCAAA[A/C]AAGTTCCTCAATCTA | 21888 |
rs36546697 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14577824 | AGTCCCTGCCTTCAG[C/T]CTTTGCCTGGTCCAC | 21888 |
rs36547422 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14575233 | AGTCTGGATGTACAG[A/G]TACATATCAAGGTAG | 21888 |
rs36550173 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14491693 | ACAAAAGTAAGAAAA[A/T]CTGCCTTTTTGCCTA | 21888 |
rs36551907 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Tle4 | Mm_Celera | 19:14530619 | TGAAAATACTAATGA[C/T]ACTAATGATACTAAT | 21888 |
rs36553145 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14502810 | ATGGCATTCTCACCA[C/T]TGCCTAGGAGCAGGT | 21888 |
rs36553255 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14572230 | TGAGTTACTTTAAGA[A/G]TGCAGTCATCTCCCT | 21888 |
rs36558923 | snp | A/C | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14471160 | TATGATGATTAAGAC[A/C]CTGGGAAAGATTATT | 21888 |
rs36566708 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14573139 | AGTACACAAAAAGCA[A/G]TACTATTGAAACTTC | 21888 |
rs36569337 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14504913 | GGGGGAGCAGAACAA[C/T]TTACATTTCTAAGAG | 21888 |
rs36581022 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14472923 | TTTATTGATGCTACA[A/G]CGGAAGTCCTGAATC | 21888 |
rs36583858 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | Mm_Celera | 19:14564213 | ATTTAAATTACATCA[C/T]AGTAAACATTAATAA | 21888 |
rs36587994 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14576914 | CTATAGTCATTTAGA[A/T]GTCTTCCTAGATCTT | 21888 |
rs36590477 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14570550 | AAACAAATTCCAAGA[A/T]GATGCTGAGAGACAC | 21888 |
rs36590865 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14538697 | TTCATATCATATGCA[A/G]TAGAAAGTAACAATA | 21888 |
rs36594549 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14453283 | GACAACATTCATTAT[A/G]TAAAAATGACCTTCA | 21888 |
rs36596889 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14496318 | TCAAGTAGCACGAGG[C/T]CTGGCTTAAGACTTA | 21888 |
rs36604148 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14499587 | AAGCTACAAGGTTCT[C/T]CCAGTGTGATCTCCG | 21888 |
rs36609877 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14514861 | AAATGTAAATAGCAT[A/G]AAGTGTACAGTGGTA | 21888 |
rs36611329 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14465624 | CTCAGGAAATTATTT[A/G]TAAGAATCTGGTCTC | 21888 |
rs36613058 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14576998 | TACTACTATGAGACA[C/T]TGAAAATAACATGAA | 21888 |
rs36614253 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14519282 | TAACTAAAGTATATC[A/C]TGAATCAGTTCTTTT | 21888 |
rs36619181 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Tle4 | GRCm38.p3 | 19:14459565 | ACTGTAATTCTACAG[A/G]GGTCTAACCGGCATG | 21888 |
rs36633159 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14454356 | CCCTGTTCATGAGTT[G/T]GTGGAAATCTTAGGT | 21888 |
rs36636460 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14558711 | GGGACATTTTAAAAA[C/T]ATTGTAGAAATGAGC | 21888 |
rs36636888 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14491957 | CTCTATATCAGAAAA[A/G]TAACTCTGTGTGTAT | 21888 |
rs36647558 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Tle4 | GRCm38.p3 | 19:14548118 | CCAGCCAGTCAGCAG[A/C/G]AGGGAACCGTCCTCT | 21888 |
rs36647722 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14479802 | AGGGACAGATTCACT[C/G]CAGAGCTTCAGTTTA | 21888 |
rs36648717 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Tle4, Gm31441 | Mm_Celera | 19:14567200 | ATATTTCCAGTCTTC[A/G]AATCACATGGTTAAT | 21888 |
rs36650787 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14485385 | AGGCACTGCCAACTG[C/T]TCATGGCAACAGCAA | 21888 |
rs36651812 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14547367 | TTTCTAGTACCAGGA[C/T]TGTGCAACTATAGCT | 21888 |
rs36652725 | snp | C/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14513698 | AGTAAATTGATTCTA[C/G]GACTCCCTATAGTGC | 21888 |
rs36655762 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Tle4 | Mm_Celera | 19:14493226 | CCCCTACTATAGCAT[A/G]CAGGGCTATCTGCTC | 21888 |
rs36658562 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14499845 | CTGTCTGCCTATGGA[A/G]CACAAGCTAATCTAA | 21888 |
rs36660472 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14463086 | CACAACTCTAATCAA[C/T]ATTTCTGAACATTAT | 21888 |
rs36661391 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14557696 | CAAACTGTATTCCCA[C/T]GTTCTCATCTCTGAA | 21888 |
rs36663127 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14512444 | TTGGTGCAAGCACAC[A/G]CAGGTTACAGATCTT | 21888 |
rs36664321 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14576478 | TGTTGACTTATATTC[C/T]AGTACAAGCTCCTTA | 21888 |
rs36664715 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Tle4 | GRCm38.p3 | 19:14534956 | CACTTATAGTACATT[C/T]GCCAACAACCTCACT | 21888 |
rs36664985 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Tle4 | GRCm38.p3 | 19:14530366 | GCATCAAGAATGCTG[A/G]CCTCCATTACAGAAG | 21888 |
rs36666573 | snp | C/T | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14549671 | ACAAAAGCGGAGGCA[C/T]GGAGATACAGGAGTA | 21888 |
rs36668498 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Tle4 | Mm_Celera | 19:14543903 | TCAGATTGATTATCA[A/G]GCGACCCTTATTTGT | 21888 |
rs36671332 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Tle4 | Mm_Celera | 19:14543331 | TTTCTATCATGTTTG[A/G]CGTGTGAGAGATAAT | 21888 |
rs36672810 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14481763 | GTTATCCATTCAACG[A/G]TAAGGTAAGGCACTC | 21888 |
rs36674860 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14477248 | TCACTCTAGGGCAGT[A/G]GTTCTCAACATGTGC | 21888 |
rs36678898 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14514130 | ACCATATCAAATGTT[A/C]CAATGAAGCTGTGTA | 21888 |
rs36680784 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14485279 | TTATTTTTTAAATCA[C/T]GAGAGGCAGGAAAGG | 21888 |
rs36687480 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14458392 | TGGGTCACACCAGAG[C/T]CCGGACTGGGCTAAA | 21888 |
rs36687811 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14514652 | ACTTGAAAACCTTAA[A/G]ACAATGCCAGAACGC | 21888 |
rs36689955 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14498985 | ACAGAAAAGTGAAGT[C/T]GGATGCTACTGAGGT | 21888 |
rs36692630 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14579444 | CCTCCTAAACCAACA[C/T]CTACTACTCTCTTGT | 21888 |
rs36709459 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14550456 | TCAATGTGGATAGAA[A/C]ACAAAACTCCAGGTG | 21888 |
rs36712219 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14458912 | TATACTTTTCAGTGG[C/T]TCAAATGAGCTCTAT | 21888 |
rs36713064 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14468430 | CGGAGAAAGACAACG[A/C]GAAGAAGAACAGTAG | 21888 |
rs36715549 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14527047 | CGGAACGGAAGATGG[C/T]ATCACCTCAGGTACA | 21888 |
rs36717067 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14453179 | ATCCTATAACCATGT[A/G]CTATGGCTTCTCACT | 21888 |
rs36717716 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14463394 | AGGGCAGAATGCTGT[C/T]ATAAGGGCTTCTAAC | 21888 |
rs36718678 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14467011 | TAGGGTGACCACTGA[C/T]ACCTGTTATTTCTAG | 21888 |
rs36724155 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14569255 | ATACTTCTCTGTCAG[A/G]GTCAGCAAGTACTGT | 21888 |
rs36724519 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14505838 | ACTCTTCCTGTGCCA[A/T]AGATTTCTTTACTGA | 21888 |
rs36735405 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14458469 | TCCATTTGTCCTCTA[C/T]CTACCTCATGTCCTC | 21888 |
rs36743392 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14514982 | AAGCCACCAGGAGTG[C/T]TTTCATTACAGCCTC | 21888 |
rs36743747 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14458383 | CTGGCAGGATGGGTC[A/C]CACCAGAGCCCGGAC | 21888 |
rs36743910 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Tle4 | Mm_Celera | 19:14547343 | ATACTAAACGTATCT[A/T]CATAGGCCTTTCTAG | 21888 |
rs36745007 | snp | C/G/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14535027 | AAAAGAAACTGTCTA[C/G/T]GAAAAGAAAAACGGG | 21888 |
rs36750196 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14454465 | CAAACAAAGGACAAA[A/T]GGTGACAATAGTTAA | 21888 |
rs36753967 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14520864 | ACCACCGCTAGTCAT[C/T]ACCAACAAACACATG | 21888 |
rs36756870 | snp | C/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14542724 | GTAAGGTCTGCTTTT[C/G]AGAACAGTCAGATTA | 21888 |
rs36756980 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14453527 | GAGCGTCCAGCATCA[C/T]GTGGTAAATTAGCTC | 21888 |
rs36758279 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14476879 | GATTAATTTTGACTA[C/T]ATACATAACCCATGA | 21888 |
rs36759765 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14587475 | TATCCACGCTTAAAT[A/G]TGCTGCCTCACGCTT | 21888 |
rs36760773 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14516502 | TTGAACGGATGTCAA[C/G]TTTACTGTAAAGTTA | 21888 |
rs36761906 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14552005 | GCTTATACTCAGAGT[A/T]CTTTGAAGTTTATCT | 21888 |
rs36765270 | snp | G/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14548448 | TCATTGTTACAAAAT[G/T]ACTTTTAATATTAAG | 21888 |
rs36765569 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14582724 | ATCTGGTTCTATACA[A/G]AGCACAACAGCAGTC | 21888 |
rs36768858 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14527070 | CAGGTACAAGGAGCA[A/G]CTTGCTTCTGTAAAA | 21888 |
rs36775417 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14511159 | TGAAAGAAAGGGCTA[A/T]TTTTTTGTTTCTAGT | 21888 |
rs36777230 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14469013 | AAGCCTGGTGGTTCC[C/T]GGTCACAAAAGTCAG | 21888 |
rs36781353 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14465907 | CATTCTAAACACATA[C/T]ACTCGCTATCTGCAC | 21888 |
rs36782845 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14516426 | TGCAAGAAAAAAAGA[A/C]ACAGGCTAGTTAGTT | 21888 |
rs36787036 | snp | C/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14565271 | GATTCTCCTACCTCG[C/G]AACTGAAGGTTTTTA | 21888 |
rs36792354 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14480315 | CCAGGTGCCGCATAT[A/G]ACTCAGGAAAAGGCC | 21888 |
rs36797999 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14480886 | AATTAGTGAAGCCAC[A/G]TGTTGCTACTGAGCC | 21888 |
rs36798570 | snp | A/C | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14467827 | TCCAAACATCTTGGG[A/C]TTTAACATTTCTACA | 21888 |
rs36800295 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Tle4 | GRCm38.p3 | 19:14558627 | TTACCTTACTATAAG[G/T]TTTAGGTGGCTGTGT | 21888 |
rs36801407 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14500872 | GTTAGCCAAAGCCTT[A/G]CTACAAAAAGACAAA | 21888 |
rs36801506 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14515160 | TAATTAACATTTAAT[A/G]TGTATAGTTCTACTT | 21888 |
rs36807952 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Tle4 | Mm_Celera | 19:14528072 | GTACACCTGCCACAC[C/T]GCATATGCTGAAGTC | 21888 |
rs36810741 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14478971 | CCTCAGAAGCGCACC[A/G]GCAGCGCGTGTACAC | 21888 |
rs36811859 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14492340 | AAAAGCAGTAGCAGT[A/C]GATTTGGTCTGAGGT | 21888 |
rs36811860 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14574235 | AATGAGATGGATAGT[A/G]TTTCTCAAAGGTTAA | 21888 |
rs36812178 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14578832 | GCTTATAAAGTCGCC[A/C]AACAGCCAAATGTTT | 21888 |
rs36814708 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14569913 | CAATGCAAAAGACAA[C/T]ACTTGTTAGGTCAGC | 21888 |
rs36815115 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14492155 | AAGACAGAGGAATAC[A/G]GGTGGAGATAAGTCA | 21888 |
rs36818420 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | GRCm38.p3 | 19:14469924 | ATGTGACAGCCAGAA[C/T]TTCTGCTTCTATAGG | 21888 |
rs36820271 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14577149 | TATATTTAATAAATT[C/T]TCCAAAATGAGTTTT | 21888 |
rs36823743 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14561936 | ACACTATCCCACAGA[A/G]AGCTGGTGTTAAAAG | 21888 |
rs36825892 | snp | A/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14549689 | AGATACAGGAGTATG[A/T]CAGAGGTATTTCTAG | 21888 |
rs36826858 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14498830 | TACCTGTGGACACAG[C/T]TTCATAGGACAACAA | 21888 |
rs36831683 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14578196 | ATGGTTACAACAGAC[G/T]GCATGACAGAGCAGT | 21888 |
rs36835651 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14477258 | GCAGTAGTTCTCAAC[A/C]TGTGCCTTGCAACCC | 21888 |
rs36841720 | snp | A/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14548546 | CTGATAAACAGACCT[A/T]TATGAACTAGTTATG | 21888 |
rs36844046 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14504264 | CCGTCTGAACTACAG[A/G]TGGAGAAGTGGGGAA | 21888 |
rs36850511 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14477396 | AAAATTAGTATGAAT[A/C]TGCAAGAAAAGCCGT | 21888 |
rs36852266 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14569364 | AGACAAATATTCCTT[A/G]TGATAACAAATGGAA | 21888 |
rs36860328 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14518954 | ACAGCCCTCAACAGG[A/T]ATCTCTTCAACTCAA | 21888 |
rs36861929 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14482875 | TGTTCTTTGGTCCCC[C/T]GTATGTTGAAAGGTC | 21888 |
rs36864141 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14478671 | GAGTTGAGGTGTGGG[A/T]GCATGAAGGAGTTGG | 21888 |
rs36864154 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14470187 | CATATTAGATATATT[A/G]AAGAAGGTCACTGAA | 21888 |
rs36873582 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14579899 | CCCACAAAGCTATGC[A/G]TTCAAGATACAATCT | 21888 |
rs36875964 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14509330 | TCAAGTTACTATTTT[A/G]TATTTTAGAAAGCTG | 21888 |
rs36877821 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14495005 | ACTCTCCATCTCAGG[C/T]TAGTGTTCTTCCCTT | 21888 |
rs36878373 | snp | C/T | 0.396694 | 0.202437 | utr-variant-3-prime | Tle4 | GRCm38.p3 | 19:14448832 | CTCCTGTACCTACAG[C/T]TCCTAAAGAGCATGA | 21888 |
rs36880827 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Tle4 | Mm_Celera | 19:14589094 | CTGAAGGTAAAAAAA[A/C]AATTCTATAGATATT | 21888 |
rs36883814 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Tle4 | Mm_Celera | 19:14450705 | TGTCAAACTTTTTTT[A/T]TTGCAATTGCTAATA | 21888 |
rs36888862 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14565867 | CTGGCCCCATGGATC[A/G]TTTAGCCATCCTTTA | 21888 |
rs36899435 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14516428 | CAAGAAAAAAAGACA[C/T]AGGCTAGTTAGTTTA | 21888 |
rs36902490 | snp | C/T | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14565794 | ACAGACAAAGCCCAG[C/T]ACCAGTAAGCAGCAA | 21888 |
rs36903065 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14487823 | TGGTGAATGCATTAC[C/T]GGAATGTATGCCCCT | 21888 |
rs36904238 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14458411 | GACTGGGCTAAATGT[A/G]TGTATCCTACCCACC | 21888 |
rs36904381 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14479795 | ACAGCATAGGGACAG[A/G]TTCACTGCAGAGCTT | 21888 |
rs36907293 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14494691 | TTTTCTACTATACCA[C/T]GGTTAATTTGTGAAT | 21888 |
rs36907640 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14584862 | CTATATCTCTGCCTT[C/G]TCACAGGTTGAAAAG | 21888 |
rs36913154 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Tle4 | Mm_Celera | 19:14586301 | ATGTGACCTCACTCA[C/G]GCCTAGGCACTGCCC | 21888 |
rs36915450 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14498866 | ACTAAAGGGAGCACA[C/T]GCCAAAATGAACCAA | 21888 |
rs36919200 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14582341 | CAGGTGAATAGTCCT[A/G]GTTTGAGACTCTTGC | 21888 |
rs36920452 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tle4 | Mm_Celera | 19:14584994 | CTTTCAACATTATTC[C/T]ATCTCACTACTTAAA | 21888 |
rs36925688 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14504354 | ATCAAAGTCTCCATA[G/T]TCCTCTTGTTTTGCT | 21888 |
rs36927439 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14497549 | TTACTTACAATAATG[A/G]TATTTGTTATTATCA | 21888 |
rs36932082 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Tle4 | Mm_Celera | 19:14478310 | TTTAGACTACTGTCT[A/T]AAGTTTTACTGTCTT | 21888 |
rs36932308 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14566740 | GCATCATTTATTTTC[A/G]GGCCTTTCCACTGGG | 21888 |
rs36934092 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14512723 | AGTCATCTGTGCAGA[A/C]TAAGCAACTAACATA | 21888 |
rs36938002 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | GRCm38.p3 | 19:14483554 | GAGACTCGATTACAG[C/T]GTGTAAGGAGATTAT | 21888 |
rs36940468 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14571356 | TTGTATGGAGAGTTC[A/T]AAATAAATTCTGAAC | 21888 |
rs36953419 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Tle4 | GRCm38.p3 | 19:14582777 | AAACTTGCCTCAGGG[A/G]AAGGCTCACCTAAGC | 21888 |
rs36954083 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14577803 | CCAGTGTATAGAAGA[C/T]AGCACAGTCCCTGCC | 21888 |
rs36961159 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14473479 | CTTCCTAAAAAGCAC[C/T]TTGTGACTGGTTAAG | 21888 |
rs36964685 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14517040 | CTAGAATTTCTTTTT[C/T]ACTCTTCTAGTTACC | 21888 |
rs36965645 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14589087 | ATCTCAACTGAAGGT[A/G]AAAAAACAATTCTAT | 21888 |
rs36965761 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14479502 | TCTAGTGTCTCTTTT[A/C]ATGCATGCAGATATG | 21888 |
rs36975449 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14552031 | TATCTTCACTCAAAG[A/T]TAGTAGGTTTTTCAA | 21888 |
rs36977023 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Tle4 | Mm_Celera | 19:14536131 | GTCCCGAGAGTCATG[C/T]ACAGTCAGTCACGCT | 21888 |
rs36987450 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14520807 | TGAAATACTAGCCAA[C/T]TGAGTATGTGCTCCA | 21888 |
rs36988872 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14450495 | GCCACAATGTCCACT[A/G]CTACTAGCACAGAAC | 21888 |
rs36991891 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Tle4 | Mm_Celera | 19:14537021 | ACTACTTGATGCAAA[A/G]GTGCTGTAGTTTTAA | 21888 |
rs36996392 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14519326 | GCATCTACCATCTGG[C/T]TCATACACTTAACAC | 21888 |
rs36997826 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14558691 | TAGGGACAGTAACTA[C/G]ATCTGGGACATTTTA | 21888 |
rs37006116 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14526450 | TAAATAGAAATATAT[A/T]ATGTCACTTTGGTAG | 21888 |
rs37011257 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14587070 | TACCATTCTGCTTCT[A/T]TGACAAACCAGCTAA | 21888 |
rs37012408 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14516196 | CAAATCTGATCCTTA[A/G]AAAAATATGATCATT | 21888 |
rs37015846 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14519026 | AAGACTAACATTTAT[A/G]GTCACTAAGTATTAA | 21888 |
rs37018577 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14518097 | GGAAGGAGTTACCCT[C/T]TTCCTGAATCATTTT | 21888 |
rs37019074 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14570078 | CCTCTGCTGTTGAAT[A/G]TAGTTGAAATTTCAA | 21888 |
rs37025417 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14486025 | TATGGACTGCTTTGC[A/C]CACAGGTACTAGCTT | 21888 |
rs37028165 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14570308 | GACTCTTCCTTAAGT[C/G]TGTTCTTGCTGATCC | 21888 |
rs37030165 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14554823 | TTAGATGGAAGTAAA[A/G]GACTAGAATTTTCCA | 21888 |
rs37034160 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14533979 | TCTGGATATAGGTGT[A/G]TCCTCAGTGAATATA | 21888 |
rs37035289 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14450464 | GCACAGGCCTAACAA[C/T]TAAAGGCAGACATGA | 21888 |
rs37041168 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14558954 | TTTTACATTATCACC[A/C]ATTTTTAGTATAAGC | 21888 |
rs37042728 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14583008 | GGACTTATGATCAAT[C/T]ATGTACATCTAAATC | 21888 |
rs37043034 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14484541 | TTATTCACTGAGAAT[C/T]TGAAAAGCATCCATG | 21888 |
rs37045192 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14582657 | CTAATTTAGCACACT[G/T]GTTGACAAACATTTT | 21888 |
rs37050316 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14512359 | TTAAACATGTTCAAA[A/G]CACATGCCTTTTAAA | 21888 |
rs37051255 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14450089 | CAATGAGGCAAATCC[C/T]AGTTCTTTAAACTCT | 21888 |
rs37055238 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14453027 | TTTCTATAACCCTGC[C/T]GTCCACTTGTCCTTA | 21888 |
rs37058637 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14486109 | TCTTCTCATTCTTTT[A/C]TGAAATCCTGCCTCA | 21888 |
rs37063424 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14520426 | TTTTCCATTTAACCA[G/T]GACATTTTTCAAGGA | 21888 |
rs37065754 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14482156 | GGCAGAGCAAGCTAA[G/T]GGCAAGCCACTGCTG | 21888 |
rs37072778 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14519082 | TTATGCTAAATCTAA[A/G]ACAGATAAAGAACTT | 21888 |
rs37075555 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14476668 | AGACCAACTGCCTAG[C/T]AGTTAAAATTGTTAA | 21888 |
rs37087652 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14458928 | TCAAATGAGCTCTAT[C/T]TATGTTTGCCCCTTG | 21888 |
rs37097621 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14493447 | AAGGCCCTGCAACCA[G/T]TAAGAGGAAAAGTAG | 21888 |
rs37099982 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14477549 | TTTCTCAGTTTTTCT[A/G]TATCAGCAAACTATC | 21888 |
rs37100590 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14476777 | AGGTTATTTCTCAGA[A/G]TAGAATTTGTCAATA | 21888 |
rs37101069 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Tle4 | Mm_Celera | 19:14558598 | TCTAAACGTATCCCT[A/G]TATCCCTCTTCATTT | 21888 |
rs37107615 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Tle4 | GRCm38.p3 | 19:14463049 | AAATATGGCACCTTA[C/T]ACCAACTGGACTTTT | 21888 |
rs37111621 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14517591 | TCAGCTCTTTGTCTT[A/T]TGAGCAACCCAGTGG | 21888 |
rs37117302 | snp | G/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14548498 | TCCATGAAATTGAAA[G/T]GATATAAGCCCATGT | 21888 |
rs37117670 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14478890 | GATGAGAAAGATTTT[A/G]GCACCCCATTCTACA | 21888 |
rs37121488 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14502669 | GGAGCTAGCCAACCA[A/G]AGCAGAACATAAAGG | 21888 |
rs37127107 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14488519 | AGTGCCTACACACCT[A/G]TAAGAACAGGTAAGA | 21888 |
rs37128274 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14488451 | CCCAGAGCTGATCCT[A/G]TACCACACAGCCACA | 21888 |
rs37135435 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14557868 | ATGATTCTTGAAAAT[A/G]GATATACTGACAATA | 21888 |
rs37137232 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14570170 | GAACACCCAGTGTAT[C/T]CAAAATCAAAGCCGT | 21888 |
rs37139919 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14494692 | TTTCTACTATACCAC[A/G]GTTAATTTGTGAATG | 21888 |
rs37146202 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Tle4 | Mm_Celera | 19:14587900 | TTAGAAATCACATCG[C/T]CTTTTCCCTCTCTAA | 21888 |
rs37147240 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14458618 | CACCTAGGATACCTC[A/G]CACAAGCTCAGTGCC | 21888 |
rs37148212 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14562214 | AATACACATATTTGT[A/G]GCTTAAATTTTAAAA | 21888 |
rs37153988 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14574988 | ACTGAAGATGCCAGC[C/G]GATTTCCATTGCCCT | 21888 |
rs37157712 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14535269 | ATGTTTACAGTCTCA[A/T]TTTTTATCTTGTTTT | 21888 |
rs37157897 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14466974 | CAAAAACTCCATGAG[C/T]CTGTAAGGAACATAA | 21888 |
rs37160672 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14494488 | TACCTTTTAGCAGAA[C/T]TAGCCAGAATACTGA | 21888 |
rs37161249 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14576249 | TTCAGTCAGTCTATA[C/T]ACTCATATATCCACT | 21888 |
rs37162403 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14550691 | AAATATCACCAACAT[C/T]TGGTAAAATGAAGAA | 21888 |
rs37168946 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14450976 | AGGGGAGAAGGCAGG[C/T]ATGAGTGTCATGACA | 21888 |
rs37170304 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14458954 | CCTTGCCTCCGCAGA[C/T]ACTGGCAGGACCTGG | 21888 |
rs37176261 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4, Gm31441 | Mm_Celera | 19:14566015 | TAGAACTCAGAAGGC[C/T]GAATGCTCAGTGCCT | 21888 |
rs37185102 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Tle4 | Mm_Celera | 19:14545910 | CAAGAGGCTCGCCAT[C/T]AAACATGGAGTTTTC | 21888 |
rs37188206 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Tle4 | Mm_Celera | 19:14546354 | CATTCACTTACCACT[A/G]TGTGCGCAATCTCCT | 21888 |
rs37193581 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14576525 | TATCAAAAGTTCACA[G/T]AGCTGCCCCAGTCCA | 21888 |
rs37195390 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14482478 | CTAACGAGATGTATT[C/T]TGAATGTGATAATTA | 21888 |
rs37197566 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Tle4 | Mm_Celera | 19:14536820 | GAAAGTTTGTGAGCT[C/G]TGAACTGAAAACGGA | 21888 |
rs37198047 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Tle4 | Mm_Celera | 19:14581682 | GCTGTTCCAGGGAGG[A/C]TTGCTAGGATGAGTG | 21888 |
rs37205578 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14486492 | AATACTGTTTCAATC[A/G]TAAGATTATCTTTGA | 21888 |
rs37206103 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | Mm_Celera | 19:14562819 | CACTCGCTAGTGTAG[A/G]AGAGGCCAAGAGAAA | 21888 |
rs37208188 | snp | C/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14493631 | ATATCAAAAGAGAGA[C/G]TTTATACATATAAAT | 21888 |
rs37210243 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14547996 | TAAAGTGTTTCACAC[A/G]TTTTTAGAATGCTGA | 21888 |
rs37212053 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14561709 | CCTGTCAGATTCCAG[A/G]ATCCACTTTCAGATG | 21888 |
rs37213552 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14578844 | GCCCAACAGCCAAAT[A/G]TTTCCCTTAAAAGGA | 21888 |
rs37227979 | snp | A/T | 0.18 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14526756 | TGCTAAAGGACATTC[A/T]ATAGGCAGTTGGACA | 21888 |
rs37235375 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14481595 | CTCATCTTGCATGCA[C/G]ACATGTGCACTAACG | 21888 |
rs37236347 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14507574 | CTAAATACAAAGTGG[G/T]GTTATTAGCCCACCA | 21888 |
rs37237028 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14515369 | TAGTTTTGTATATAC[G/T]TCACAAAAAACAGCA | 21888 |
rs37239217 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14557924 | CAAATTACTTTCGTA[A/G]TTAGAAGACAGCTAC | 21888 |
rs37240940 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Tle4 | Mm_Celera | 19:14545148 | CACTCTACCATCCGC[A/C]AGTATGAAGACAAAG | 21888 |
rs37242483 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14480991 | CATAGCCTACAGTAT[C/G]AATAAAGTAAATTAA | 21888 |
rs37243053 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14459690 | TATCCACTCTACTAC[C/T]TCTAATGGCTACTTA | 21888 |
rs37262190 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14579962 | ATTTAAGGAGTTAAC[A/T]ATGTCAATTTATAAG | 21888 |
rs37262904 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14507675 | GGTCTCAACAAAGTA[A/C]CAAGTTAAAGAAGAA | 21888 |
rs37266406 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14492566 | TGCATGAGGAAGGTC[A/T]GGAGTTGCTGTCCAA | 21888 |
rs37269038 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14568747 | ACAAAGCTATTTCAG[C/G/T]CTACGCCTGTGTCTT | 21888 |
rs37274489 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tle4 | GRCm38.p3 | 19:14483866 | CTTGATGTTCAGTGT[C/T]GACATCAGTCCACTA | 21888 |
rs37274898 | snp | A/T | 0.124444 | 0.216185 | missense | Tle4 | Mm_Celera | 19:14517806 | ATGGTGCTTCTTCTC[A/T]TCCTTAATTGGGAGG | 21888 |
rs37277723 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14484671 | AGGATTTGGTTACAT[A/T]ATAAAAGTCGAAGGA | 21888 |
rs37281094 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14584509 | CAGATCCTAAGAGAA[C/T]CAAAACACTCCAAAC | 21888 |
rs37283945 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14488501 | GAGAGCTGGTCTTGC[A/T]GGAGTGCCTACACAC | 21888 |
rs37295880 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14568575 | TAGTGCATGATAAAA[C/T]GTGCTATCAAGTGCC | 21888 |
rs37303854 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14569347 | CACACACCTAGGCAC[A/G]GAGACAAATATTCCT | 21888 |
rs37305141 | snp | A/T | 0.277778 | 0.248452 | stop-gained | Tle4 | Mm_Celera | 19:14453799 | CATCAGGGAGCAATC[A/T]GCAGGAACGGATGTA | 21888 |
rs37305526 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tle4 | GRCm38.p3 | 19:14488652 | TCTACATCCCAGAGC[C/T]GACATTGTACCACAG | 21888 |
rs37308170 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14571296 | ACTGATCATCTGAGA[C/T]TTTGGCATTCAGCAC | 21888 |
rs37308726 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | Mm_Celera | 19:14563870 | CACAGAAATGTGTAC[A/G]CTGGATTTACCTTGG | 21888 |
rs37310848 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14482271 | ATTAGCTCAGGGAGA[A/T]CCTAGACTTTCTCAC | 21888 |
rs37314248 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14560834 | GCAGTTCTGGGTCTT[C/T]CCCCAAGAGAACTTA | 21888 |
rs37315440 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14507492 | CACTCAAGAAACAGA[A/C]GTGTTTTTAAAAGCT | 21888 |
rs37315634 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14451618 | GGCTCACAGGACACG[C/T]GCTGCTCAGCAAGCA | 21888 |
rs37318789 | snp | A/C | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14518815 | GCAACACATAGAGAA[A/C]GCCCTTAAGAGGTTG | 21888 |
rs37323188 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14488757 | GCAAGACCAGCTAAA[A/G]CCAGAGATAGTCAGA | 21888 |
rs37327013 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14453372 | TAAAAGATAGTGTGG[A/G]AGAAAGATTTCACAT | 21888 |
rs37328081 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Tle4 | Mm_Celera | 19:14512904 | GACTTTAAAATTAAG[C/T]ACAACATCTGTACTT | 21888 |
rs37333633 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tle4 | GRCm38.p3 | 19:14516117 | AAGTTAATACATTTA[C/T]TCCACTGCAGTATCT | 21888 |
rs37339174 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14486824 | ATGTAATTCACCAGG[C/T]TCAACTGTGCTGCTA | 21888 |
rs37347781 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Tle4 | Mm_Celera | 19:14504581 | GCCTCACAAAAATAA[A/G]GACCTTATCTCATGT | 21888 |
rs37348131 | snp | C/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14565819 | CAGCAATGACTGAGA[C/G]TCCACTGTGTTGACC | 21888 |
rs37363558 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14499238 | AGTAGTACAGTGCAG[A/G]GATGTGTACTCTTTC | 21888 |
rs37366568 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14499832 | TTCTTTCTGCTGTCT[A/G]TCTGCCTATGGAACA | 21888 |
rs37366607 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14572751 | TTCCCTGCTGTTCTA[A/G]GTTAAACACACAAGG | 21888 |
rs37367519 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14583328 | TTGTAACTGTCTACA[A/C]TATCCTAACATTGTT | 21888 |
rs37372882 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tle4 | GRCm38.p3 | 19:14559421 | TGCAGCCTTACAAAG[C/T]CCAGGATTCTGCTCA | 21888 |
rs37377487 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14562241 | AAAAGACATACTCCA[A/G]CTTAGAAAATGAGAA | 21888 |
rs37384128 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Tle4 | GRCm38.p3 | 19:14503308 | TCCAAATTATGAGCC[A/G/T]GGATATTACTTCCAG | 21888 |
rs37385462 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14583709 | TAGAAAATAATCCAC[G/T]AATTCTACCTTTCAC | 21888 |
rs37385712 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Tle4 | Mm_Celera | 19:14457662 | CTCCTCTACTCCCAG[G/T]TTTCCAGCTATGGCC | 21888 |
rs37389344 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14584742 | AGGAACTTTCTGTGC[A/G]GAGTATAGTTCAGGA | 21888 |
rs37390088 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14488777 | AGATAGTCAGATGGC[A/G]AAAGGCAAGCTCAAG | 21888 |
rs37393180 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14519245 | TTCTTTCTTCGTCCT[C/T]GACTGTGTGCCTTCC | 21888 |
rs37395637 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14462433 | AAGAGCCAGAGGTAG[C/T]AGATGATTCCAAGGG | 21888 |
rs37398461 | snp | A/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14560036 | CTTATACAGGAACAC[A/T]GAAGGCTTACAGAGA | 21888 |
rs37407744 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Tle4 | Mm_Celera | 19:14546856 | CAGTGCAATGAAAAG[A/C]AGCAGCACTTGCAAA | 21888 |
rs37416832 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Tle4 | Mm_Celera | 19:14545271 | TTTTTAAATTCTCCT[C/T]AGGTGTTTATTAGCA | 21888 |
rs37417677 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14465695 | TGTGGGCTAATGCTG[C/G]TGGCCATGGTTAAGT | 21888 |
rs37418278 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14525237 | ATTCAATTTTGCATG[C/T]GTTCTCTATTAGTAA | 21888 |
rs37421865 | snp | G/T | 0.42 | 0.183303 | intron-variant | Tle4 | Mm_Celera | 19:14545894 | AACTGCTTACAACAT[G/T]CAAGAGGCTCGCCAT | 21888 |
rs37424472 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14577347 | GACTGGGGCAGAGAC[C/G]ACCAAGTTCTGAAAA | 21888 |
rs37430619 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14463196 | CTACAAGTAAACTTT[C/T]AAAAGCTGGGCATGA | 21888 |
rs37432188 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14575739 | AAGCAGGAGATGTCA[A/G]ACTTTGGTGCACTAT | 21888 |
rs37435941 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14519920 | ATATAGAAAAGTTAG[A/G]CGGTTCCTCACAGGA | 21888 |
rs37461758 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14541370 | AAGCATTTTAAGATA[A/G]TCAGATGACTCAATT | 21888 |
rs37461989 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14492457 | CTAGATCTCAGGGCA[C/T]GCTCTGCAGACCCTT | 21888 |
rs37462999 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4, Gm31441 | Mm_Celera | 19:14566670 | CGGAAACACTGCTGC[C/T]TCCATGGTCATCTAA | 21888 |
rs37474565 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14462582 | GTGGCCCACCACTAA[G/T]TAAGATGCTGTTTAC | 21888 |
rs37482082 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Tle4 | Mm_Celera | 19:14545337 | ATCTCTGCGGGAAGT[C/G]TAAAAGTCTATGTTT | 21888 |
rs37483873 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14492181 | AGTCAGTGATCTACA[G/T]CAAAAGCTGACACTC | 21888 |
rs37484629 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14500086 | CCTTCAGAAACCAGG[C/T]TCAAACAGTATGTAA | 21888 |
rs37489728 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14557618 | AGGTTATTCATCTAT[A/G]TCAGTTATACTCTGT | 21888 |
rs37490898 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14458270 | CCAGGCAAGATGATG[C/T]AAAACAGCCCAGAGC | 21888 |
rs37498385 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14491839 | CTTGGTATTGAAAAC[A/G]TACAATTTTGTAATT | 21888 |
rs37499721 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14572203 | TTGTTATCTATTTGT[A/G]TTTCTATAATCTGAG | 21888 |
rs37509307 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14514525 | CAACAACCATAAACT[A/G]CACCCTCTTAAACAG | 21888 |
rs37518230 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14450524 | ACACGAGAACAGGAA[A/G]GAGGAGTTCAATAGT | 21888 |
rs37521345 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14570060 | TCTAATGTCTTCATC[C/T]TCCCTCTGCTGTTGA | 21888 |
rs37526946 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14519005 | GAACAATTGCTGGGT[A/G]AATCTAAGACTAACA | 21888 |
rs37530868 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14496373 | CGGATGCAGAAACCA[C/T]CCAAAAGTGTCAAGC | 21888 |
rs37531295 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14483049 | ACATGTCATACAAGG[C/T]TCCACCAAAGGATGA | 21888 |
rs37551765 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tle4 | Mm_Celera | 19:14453148 | GAAGTGTGCCCCATG[C/T]GTCACCTAAATTATA | 21888 |
rs37556383 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14517315 | AATAATAACTGATTT[A/G]GTCAAATATAAATAA | 21888 |
rs37557780 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14482458 | CATTGTGTCACTCTA[C/T]AATGCTAACGAGATG | 21888 |
rs37561110 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14533894 | CTCAATTTTGAAAAA[A/G]TAAAAGTGTGCACTT | 21888 |
rs37565741 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14550360 | AAAATAGTATACTGG[A/G]TCTTCAGCTTACTTC | 21888 |
rs37566595 | snp | C/T | 0.42 | 0.183303 | intron-variant | Tle4 | Mm_Celera | 19:14541953 | CCTGTCTTGATGGTG[C/T]GCATACATATAAAGC | 21888 |
rs37566746 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | Mm_Celera | 19:14562892 | CACCTGCGTCAGGGG[C/T]GGAGGAACTTGATCC | 21888 |
rs37577118 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14455536 | GCAGAGAACTAAGTA[G/T]GATAGCTAATGACAT | 21888 |
rs37581847 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14513196 | GATACAGAAGAATGC[C/T]ATATTAAGAGAAATC | 21888 |
rs37584828 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14488423 | AACAGGAGTCTTCCG[A/C]TCTCCTTCTGAGCCC | 21888 |
rs37591339 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14566803 | ACACTTCTAATGGCC[C/T]ATGTTTTGAAACTGA | 21888 |
rs37591585 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14513678 | GCTTTAGTTTCTCAT[A/G]ACCAAGTAAATTGAT | 21888 |
rs37599701 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14575386 | GAATTCCCAGATCTG[A/C]AAGTTATTTTCTAAT | 21888 |
rs37602509 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tle4 | Mm_Celera | 19:14583301 | ATCATGAATCACTGG[C/T]AAAAGTAATTATTGT | 21888 |
rs37602828 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14527771 | AAACAAATACTATGT[A/G]TACACTATGTTTTCT | 21888 |
rs37603793 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14482101 | CAATTATATTTCCAA[A/G]ACTCCTGGGTGATTC | 21888 |
rs37611962 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14496227 | TAAGCTGCTCTTGAA[C/T]TCACTCTGTAGTCCA | 21888 |
rs37612029 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4, Gm31441 | Mm_Celera | 19:14566469 | CATCCCAACAGAAAA[A/G]GAGTAAAATCTTCAA | 21888 |
rs37613469 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14495484 | TACAAAGAGTTCAGA[C/T]CCAGAGATGGCTTAG | 21888 |
rs37615783 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14579487 | AAGCCTGGAAATGGT[A/G]ACCCAGTGTGAACAT | 21888 |
rs37636823 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14570499 | GGGAATCTTGGTATA[A/C]AGCAGATAGAGTTGG | 21888 |
rs37638745 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14510786 | TGAATTTTGTGAATA[A/C]TTACAAGTTCATTTA | 21888 |
rs37641174 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14575881 | AGCAGCTTCCGGGTG[A/C]AGGAGAGACAATTGG | 21888 |
rs37641256 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14454441 | AAAAGTAAGCTTCAA[C/T]TTCCTGTGCAAACAA | 21888 |
rs37649477 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14510714 | TTAGATGAAGAAAGG[A/T]TTAAGAGTTATCACA | 21888 |
rs37653009 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14518917 | GGGCAAGGGAGAAGA[C/T]AGGGAGGATGCGGAG | 21888 |
rs37653248 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14569284 | GTCAGCTACTTTCTT[C/T]TCATAAATATACTGG | 21888 |
rs37653682 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Tle4 | Mm_Celera | 19:14531979 | ACTAATTTAGTATGT[A/G]TATCAGTCACATTCA | 21888 |
rs37661940 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14514666 | AGACAATGCCAGAAC[A/G]CACACAGCACACTTC | 21888 |
rs37668135 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14504323 | CCTGAGTGAGAATCA[C/T]CTGAAAGTGACACTG | 21888 |
rs37673572 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14450836 | GTATTAAAATTTAAG[C/T]TTCAGCCAGGCATGG | 21888 |
rs37673699 | snp | A/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14472406 | GCATCCAAGATAAGG[A/T]ACTAAAAATCTGCCC | 21888 |
rs37686889 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14580805 | ATTATTATTTAGGTT[A/G]ATCAAGGTAGACATG | 21888 |
rs37687902 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14574341 | CCTGATCCTACCACA[C/T]CAGCCCGGGGCACGT | 21888 |
rs37690753 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14507087 | CAGTGAATAGATCAA[G/T]AGAAGCAACAGCTTA | 21888 |
rs37693991 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14573457 | TTGTTAGGTAGCAAC[A/G]ACAATTAAAAGACAA | 21888 |
rs37695174 | snp | C/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Tle4, Gm31441 | Mm_Celera | 19:14567369 | GTTCGTTGTTAGAAT[C/T]ACATGGTGTTATTAT | 21888 |
rs37706951 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14487480 | ATGGCATCCATGACT[C/T]GACATTTACCTAGAG | 21888 |
rs37715066 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14499120 | TAAACGCTGCAAAAG[G/T]CCCCTTCCCTGCACA | 21888 |
rs37718405 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Tle4 | GRCm38.p3 | 19:14575544 | AAAAGCCTTTAAGGT[A/C]AATAGTTACTTTAGA | 21888 |
rs37723890 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14488199 | TTACAAAGCTATATG[C/G]TGGTATAACTTACAA | 21888 |
rs37724434 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14501988 | GGAAGGTGAAATACA[A/G]CATGGCATTTTTTTA | 21888 |
rs37724613 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14568548 | TGTTTTGAACTCACT[C/T]GTATGCCATTTTAGT | 21888 |
rs37726909 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14587423 | CTGACTTTTAAAGAA[A/G]TCCTAAACCTTACAA | 21888 |
rs37727542 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Tle4 | GRCm38.p3 | 19:14585329 | TTTCAAAAATATGCA[C/G]TAAAGAGGGTTCAAA | 21888 |
rs37736072 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14514688 | GCACACTTCAAGCAT[A/G]GACTTGTAGCTGTCA | 21888 |
rs37744021 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14476201 | TATATAAATCTGACT[A/G]TTTTGAAAACCAAGG | 21888 |
rs37745714 | snp | A/T | 0.260355 | 0.249785 | downstream-variant-500B | Tle4 | Mm_Celera | 19:14447901 | TTGAGAGTTTTGGAC[A/T]GCTTCTAGATGAAAG | 21888 |
rs37746436 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Tle4 | Mm_Celera | 19:14481878 | AATGAAAACGGTTTT[C/G]TTTTGTTTAGGATCA | 21888 |
rs37756826 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14521432 | TATTTTTATTGATGA[A/G]CTTTTTATTTTTCAT | 21888 |
rs37758666 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Tle4 | Mm_Celera | 19:14536180 | CTCTCCCTTAGATCC[C/T]GGGTTTGTTCTACCC | 21888 |
rs37759145 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14580846 | TACACTCTAAACATG[G/T]CCATCAAACCCAAAC | 21888 |
rs37764255 | snp | C/T | 0.42 | 0.183303 | intron-variant | Tle4 | Mm_Celera | 19:14449901 | AGCAGGACTGGTGGG[C/T]GTGGCTGAGCAGATG | 21888 |
rs37764558 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14496566 | TCTTTTTGTGGAGAG[A/G]CAAGAGAAGGTAGCA | 21888 |
rs37765392 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14503124 | TGCAAAAGTTCCCAG[G/T]TCTGTTTTGATTCCT | 21888 |
rs37772977 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Tle4 | Mm_Celera | 19:14514613 | TCACAGAAACATGGG[A/G]AAAAAAATTAGCCAA | 21888 |
rs37776671 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14453487 | AAACACACAAACATA[C/T]GACACATAGTAAGAC | 21888 |
rs37782530 | snp | A/C | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14481393 | AGTCTGAAGTACCTC[A/C]TGAGAATACTCTTAG | 21888 |
rs37784269 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14575314 | AGTATGGGGACAATT[C/T]AGCCTCAGATGACTA | 21888 |
rs37786718 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Tle4 | Mm_Celera | 19:14516880 | AATGGTAAAAGACTT[A/T]CTCTCTCTCTCTCTC | 21888 |
rs37789599 | snp | A/G | 0.18 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14536873 | GAGAGCCTTTGTTAC[A/G]AGAGACATCAAAGCC | 21888 |
rs37797999 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Tle4 | GRCm38.p3 | 19:14587930 | ACTAGCAAATCATTA[G/T]TAACCCAAAGTCTCA | 21888 |
rs37811861 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14492589 | CTGTCCAATGACCAT[A/G]TTTATCAGACAGCCA | 21888 |
rs37812410 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14575510 | ATGGCAGAAGTATTC[A/G]TGTGGGTCAGGTATG | 21888 |
rs37814272 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14484981 | GTGTCGTCTCCTCAT[C/T]CCTTTCTTCTGCGTA | 21888 |
rs37816676 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14548318 | GCAGAGTTACTGAAA[A/G]CCATTGAGTTACATG | 21888 |
rs37824897 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14483680 | ACTAGAGAGGGGAAA[C/T]AGAATCTTTGACCTT | 21888 |
rs37827791 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14498747 | ACAGGCTATATCCCT[A/G]TTGGTTTTATCAATA | 21888 |
rs37830175 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14517201 | GTTAATCTCATGCTT[C/T]GAATAGCAGTAACTC | 21888 |
rs37836859 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14480829 | ACAAATGATTGTAAC[A/G]AGAAAGCAAGTACAA | 21888 |
rs37840759 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14458401 | CCAGAGCCCGGACTG[G/T]GCTAAATGTGTGTAT | 21888 |
rs37851644 | snp | A/C/T | 0.336735 | 0.234472 | intron-variant | Tle4 | GRCm38.p3 | 19:14588805 | TCCAGCAATGAGCTC[A/C/T]GGCCTAAATCTCTAA | 21888 |
rs37852368 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14488748 | TCAGAGACAGCAAGA[C/G]CAGCTAAAACCAGAG | 21888 |
rs37856226 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14558930 | TTGCGCTCTGTTAAA[A/C]TAGGTCTTTTTTACA | 21888 |
rs37857986 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14459461 | GTCCATTTGCTGTAG[C/T]AGTGGAAATCTGTGG | 21888 |
rs37860462 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Tle4 | GRCm38.p3 | 19:14477722 | CACATGTGAGTTTCG[C/T]TATCTAGGCCGGACA | 21888 |
rs37861045 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14487998 | AAGCAAGCAAAACTA[C/G]TAAGATTAAGTGGCT | 21888 |
rs37861984 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14530893 | TACTCATAAGCAACA[C/T]AGAAACACAAGACAA | 21888 |
rs37868599 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Tle4 | Mm_Celera | 19:14557622 | TATTCATCTATGTCA[A/G]TTATACTCTGTTTTA | 21888 |
rs37868992 | snp | A/C | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14565241 | CTTTTTTGGAAATAC[A/C]GGGACAATGCACATG | 21888 |
rs37876173 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14577414 | CTAACTGCCTCTAGG[A/G]CCTGTAGGGTACCTG | 21888 |
rs37881034 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4, Gm31441 | Mm_Celera | 19:14566153 | CTGCCAAGCATATTT[C/T]CCTCATTATGTTGTT | 21888 |
rs37888002 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Tle4 | Mm_Celera | 19:14579872 | ACCCTTCCAACAGAG[A/G]AATTATGTAACCCCA | 21888 |
rs37905771 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14485063 | AACCCAACTTCGTTA[C/T]GGTGATTTATAGGAG | 21888 |
rs37906251 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Tle4 | Mm_Celera | 19:14582800 | ACCTAAGCGTGGTTC[A/C]GAATTGAGCTCTGAA | 21888 |
rs37907175 | snp | C/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14458018 | GGGCAAGAGTTAAGG[C/G]CCTTCTCCAAGGTGG | 21888 |
rs37907485 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Tle4 | GRCm38.p3 | 19:14456865 | TATGAGATCTGGTAG[A/G]AATGCTGGGAGTAGG | 21888 |
rs37913057 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14459884 | AATCTTTCACCTTCA[C/T]AGTTCTTGGCCAACA | 21888 |
rs37918924 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14468286 | TCTGGAATTAGAAAT[A/G]GAAGCGGGATTGAAA | 21888 |
rs37922341 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14506349 | CAGGGAGACCATGCT[G/T]TTAAATATCAGCAAT | 21888 |
rs37934224 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14536104 | ATTAAAAGTCCTTAC[A/G]CCTTTCCCAAAGTCC | 21888 |
rs37939720 | snp | G/T | 0.277778 | 0.248452 | utr-variant-3-prime | Tle4 | GRCm38.p3 | 19:14449700 | CAGCGCAAAGTGCTA[G/T]GAGGAGGAGTCCAGT | 21888 |
rs37946474 | snp | A/C | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14521215 | TAAGGTCAGCACCAT[A/C]CTATAAGCAGATGAA | 21888 |
rs37964046 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14584266 | AGTAATCCCTAGGGT[C/T]AGTTATTCAACAGGT | 21888 |
rs37972949 | snp | C/G/T | 0.48 | 0.0979796 | intron-variant | Tle4 | GRCm38.p3 | 19:14578792 | TAATAATTATGGCAA[C/G/T]AATCACACAAAATGA | 21888 |
rs37980596 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14487381 | GAGCACCATGACGCG[C/T]GCACACTGGACTCCA | 21888 |
rs37983906 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14475836 | TTCATAGTGATTATA[A/G]CAATTTTTACAGAAA | 21888 |
rs37992418 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14514343 | CCTGTTTGCAGATTA[A/G]AAGAGGAAAGGGAAA | 21888 |
rs37994769 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14502795 | AGGTCTAACCTTTGC[A/G]TGGCATTCTCACCAC | 21888 |
rs37995017 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14518171 | TGCTTTTCTTCTAAA[A/G]TCTATGGGTTTTGTT | 21888 |
rs37996883 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14462527 | ACATATGACCTGCAA[A/T]AGTTCAAGCCAGATA | 21888 |
rs38005027 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14478233 | ATAACTATTTTCATG[A/G]ACTGACTAGTGAAAA | 21888 |
rs38011694 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Tle4 | GRCm38.p3 | 19:14572819 | GGAATTTCAAGTATT[A/G]AAAAAAAATGTATCC | 21888 |
rs38011805 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Tle4 | Mm_Celera | 19:14545391 | GTGCTTAAACAAACA[A/T]GCAAATGAAATGGAA | 21888 |
rs38017131 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Tle4 | GRCm38.p3 | 19:14478977 | AAGCGCACCGGCAGC[A/G]CGTGTACACACACAC | 21888 |
rs38022147 | snp | G/T | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14565658 | CAGCCCTTTTAACTT[G/T]GTAAGCATGCAATTT | 21888 |
rs38024024 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Tle4 | Mm_Celera | 19:14542809 | AAACCCCGTCAGCAC[C/T]GACAGAAGCTGCTTT | 21888 |
rs38025146 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14459751 | GGACTGTACCTCTTC[C/T]CTAAAAGAGGCCTTC | 21888 |
rs38025276 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14496221 | CCTTGTTAAGCTGCT[A/C]TTGAATTCACTCTGT | 21888 |
rs38038630 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14482357 | CCATAGTTCAGAGCT[A/G]TGAGGAAGAAAAACT | 21888 |
rs38045418 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14456002 | CACTTCCATTTCCAG[C/T]TGACAGCCTTAGAAA | 21888 |
rs38051300 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tle4 | Mm_Celera | 19:14583961 | GCAGTGACTTTACAC[C/T]ACACATGAAAGAAGT | 21888 |
rs38058029 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14578719 | CCTATATTAATATTC[A/G]GAATATCTCCAAAGA | 21888 |
rs38058908 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14501771 | TGTTCCAGTAAATGA[C/T]TTCCCCATTTTCCTG | 21888 |
rs38060708 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14450756 | ATATACATCGATATA[A/G]TACTTGTATTTAATA | 21888 |
rs38071955 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14568677 | TTGGTGCTGTTCACG[A/C]AGCAATATGCAGCAG | 21888 |
rs38072409 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | Mm_Celera | 19:14564295 | CATCAAGAAAATGAC[A/G]AGACCAGAATTGGGT | 21888 |
rs38075849 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Tle4 | Mm_Celera | 19:14527592 | TTATGTTTGCTTCAC[C/G]TTTGTGTGTTGTGCA | 21888 |
rs38087790 | snp | A/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14549865 | AGTTTCTCGAGTTTA[A/G]TAAGATGGACCTTAC | 21888 |
rs38100823 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14497389 | AACTGACAACAGACT[C/T]TATCTAACACCTCAC | 21888 |
rs38101861 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14542637 | AGTCAGCAGCAGAAC[A/T]GGTCACATGAGTTTG | 21888 |
rs38103383 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14558580 | GTTATGCATAGCGCT[A/G]CATCTAAACGTATCC | 21888 |
rs38106724 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | GRCm38.p3 | 19:14463045 | CATCAAATATGGCAC[C/T]TTACACCAACTGGAC | 21888 |
rs38112639 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14531255 | AATAACAACATGGAG[A/G]CATTTTATTAATTAT | 21888 |
rs38113800 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14480802 | ATGTGCACAGCCAGC[C/T]TCTGAAATCTGACAA | 21888 |
rs38124640 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14547532 | GGAAGCTAACATTAA[A/T]ATGGAAGTCATGACT | 21888 |
rs38128302 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14492819 | AATGGAATACAACAA[A/G]TGAGAAAATCCTGCA | 21888 |
rs38140186 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14458275 | CAAGATGATGCAAAA[C/T]AGCCCAGAGCTGGTC | 21888 |
rs38146760 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14533848 | AAGTAAAAAACACAC[A/G]AGAAAAAAACAATTA | 21888 |
rs38148742 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14571532 | TCCCACGAACTACAC[A/G]TGCTACAGTATATTC | 21888 |
rs38152304 | snp | A/G | 0.18 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14528004 | AGACTGATGATGGGA[A/G]CTAGAGTAACTTTGC | 21888 |
rs38154243 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14466257 | TGACAGCTAAACTCC[C/T]GAGCGAGTTCACCAC | 21888 |
rs38157091 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14513822 | ACTGAAGCTAAAGAC[C/G]ACTAGATCAATAAAG | 21888 |
rs38159045 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14561041 | TAGCTGGGAAGCCAG[C/G]ACCCGATTCCTGGTC | 21888 |
rs38159606 | snp | A/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14562313 | TGTGATATAGGCTCA[A/T]AATGTATACCAAAGA | 21888 |
rs38159895 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14518535 | TTAAGCCCTTTAAGT[A/G]TCCTCAGCGGCACTT | 21888 |
rs38161986 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14515744 | CACCTTTATGCACGC[A/T]CATGGCATATTTAAG | 21888 |
rs38174039 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14484921 | ATTCCCGTCTATGTA[C/T]GTAAATTTTGATCAT | 21888 |
rs38175793 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14477228 | GAGGATACGCCTAAG[C/T]CTTTTCACTCTAGGG | 21888 |
rs38176480 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Tle4 | GRCm38.p3 | 19:14462425 | AAGATTCTAAGAGCC[A/G]GAGGTAGCAGATGAT | 21888 |
rs38181887 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14543922 | ACCCTTATTTGTATC[C/T]TCACTTAGCAATTTG | 21888 |
rs38194346 | snp | C/T | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14468352 | TTTTGTTCTGCAGTA[C/T]ATGCCCAGGAAGCTA | 21888 |
rs38198201 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14584032 | ACATTCCTCTATTAT[G/T]TTATTTACCACTGTC | 21888 |
rs38204776 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14493408 | TGTTAAATACTAGGT[G/T]ACCATGGGAGACAGG | 21888 |
rs38208354 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14552723 | AGTAAGAAAGAGCCT[A/G]ATCACATTTTTCAAC | 21888 |
rs38213756 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14469336 | GAACCAATACCTCAA[C/G]TTGTTCACTAAGCTC | 21888 |
rs38217075 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14501936 | GCCCAGAAACTATTT[C/G]CGTTCTATCATTACT | 21888 |
rs38219637 | snp | A/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14467462 | TACAATGGCCTGCTT[A/G]CTACTCTAGAACCCA | 21888 |
rs38249550 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14550148 | ATCATCCACAGGTCA[A/G]AAACCACTAGTATAT | 21888 |
rs38250109 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14512857 | ATATGCATACACACA[C/G]AAAAGCATTTAGTGT | 21888 |
rs38267906 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14582587 | GCCTGTGATCATCAG[G/T]TAAACAACAAGCTAT | 21888 |
rs38272626 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14491805 | GAGTCATGAACTGCC[C/T]GGTCTTTTAAAAATA | 21888 |
rs38302291 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14480517 | TCTGGAACTTGTCCT[A/G]AAAGGAACAGGCCAC | 21888 |
rs38311602 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Tle4 | GRCm38.p3 | 19:14574539 | ATCCCAACAATCAAG[A/G]ACAGCCTGTGTGTAA | 21888 |
rs38323578 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14495754 | TCAGTTCCCAGGAAC[C/T]GAACGTGGTGATAAC | 21888 |
rs38324833 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14589394 | GTAAACTTGTCCCTA[C/G]TCTAAAACATCCAAA | 21888 |
rs38331863 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14458024 | GAGTTAAGGCCCTTC[G/T]CCAAGGTGGAACATT | 21888 |
rs38333254 | snp | A/C/G | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14477198 | TCCGTGATTTTACCC[A/C/G]AAGTTTCTTCCTTAG | 21888 |
rs38343446 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14584378 | CCCAAGCAGTATATG[C/G]CAAAGGAAAAATACA | 21888 |
rs38347154 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14574517 | GCTGCATCAGGTCAC[A/T]CCAACCATCCCAACA | 21888 |
rs38353026 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14521401 | TTGGTACCTCTTCAC[A/G]TAAAACTTATGGGCT | 21888 |
rs38372359 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14574206 | GGGATTTACAAAGCC[A/T]ATATAATACAGTAAA | 21888 |
rs38372796 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14463740 | AAATACTAGTCTGAA[A/G]GTTTTCTTGTCCAAT | 21888 |
rs38378699 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14517339 | TAAATAAGCCTTTTT[A/T]AAGTTTTCCTGTCCA | 21888 |
rs38395998 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Tle4 | GRCm38.p3 | 19:14542466 | AGAAGACTAGCACCA[A/T]GCTTTTgaaagaaag | 21888 |
rs38407071 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14501007 | TAAAACGGAGTACAG[C/G]AGCCCCAACAAAACA | 21888 |
rs38407463 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14496668 | TGCCATAAATCTCCA[A/C]GAGCTAGCAAGCAGA | 21888 |
rs38411474 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Tle4 | GRCm38.p3 | 19:14542016 | CTGCAGTGGCAGAGA[C/T]GGGTCTTGTGCCTCC | 21888 |
rs38422535 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14459414 | AGAAAAGCTAAGTTT[A/G]AGTTCAGGTTTCTGG | 21888 |
rs38428327 | snp | C/T | 0.152778 | 0.230321 | utr-variant-3-prime | Tle4 | Mm_Celera | 19:14449122 | TTAAAGTTGCCCAAA[C/T]AGACTCAAAGGAATA | 21888 |
rs38429173 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14562376 | AGCAAAGAGTTAAAC[A/G]TCTACCCTCTCAGCC | 21888 |
rs38476468 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14500121 | CTTCCTTGAGTCACT[C/T]TTTACAAGGATGTTA | 21888 |
rs38487145 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14483011 | TGGCTTCCTACTTCA[C/G]CACATGTATGTTCAT | 21888 |
rs38498196 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14483042 | GCCATTAACATGTCA[C/T]ACAAGGCTCCACCAA | 21888 |
rs38514326 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14492167 | TACGGGTGGAGATAA[A/G]TCAGTGATCTACATC | 21888 |
rs38527158 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14558805 | AGGACAAGAGATAAT[G/T]AACATGGAGACCAAA | 21888 |
rs38529142 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14515781 | TGACTCAAGGTGGTT[A/G]AAATACAGTCATAGT | 21888 |
rs38532179 | snp | A/T | 0.32 | 0.24 | missense | Tle4 | Mm_Celera | 19:14452445 | AAGTCATGTTGCTGC[A/T]GCTGCCGCCCTTCAC | 21888 |
rs38549075 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14484026 | TAATTTTCTGCAGCA[A/T]AACATAGCATTTAAT | 21888 |
rs38552266 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14521275 | AATTTATAATACAAC[C/T]AGAAGAAAGCTAGCT | 21888 |
rs38554721 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14574881 | ACATGTTGGGTTTAA[C/T]GATCTATGAGACACT | 21888 |
rs38571975 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14540491 | TGAGGGTCAGCAAAA[A/C]TAAGCACACACAATT | 21888 |
rs38573680 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14587020 | GACAACTCATCTCCC[A/C]GAGGACAGAGTGCCC | 21888 |
rs38584835 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14478394 | AGTGACTTGAATATA[C/G]TGGGATAAAAGCAAA | 21888 |
rs38591582 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Tle4 | Mm_Celera | 19:14449950 | CAGAGCACCAAGTAC[A/G]TCTGCAGATAGAGGG | 21888 |
rs38599547 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14488632 | AAGGATCCTTCTGGT[C/T]TCTGTCTACATCCCA | 21888 |
rs38610166 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Tle4 | Mm_Celera | 19:14525746 | ACATTTCCTGTAAAT[C/G]ACTAAAGGTGTACAG | 21888 |
rs38611837 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14476259 | GGTTAAGTAGAACTG[A/G]CTTAAGAACTATCTT | 21888 |
rs38613573 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14454252 | GCAGTTGGCTCTTTC[A/G]GCCTAGCATTGTTAT | 21888 |
rs38625100 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Tle4 | Mm_Celera | 19:14506772 | CAATGCAGCTTCATA[A/G]TTCAAATATTGCTTA | 21888 |
rs38644153 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14519456 | CTTTTCTACCTGTAG[A/T]TTTTAAATCAGACGC | 21888 |
rs38656791 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14481707 | GTAAGAGCACAGTCC[A/T]ACAGTAAGAAACAGT | 21888 |
rs38660535 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Tle4 | Mm_Celera | 19:14532762 | GACAAGAGTGACACA[C/G]AAATCAATACTAAGT | 21888 |
rs38670092 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14585399 | CTTTCAGACTGATCA[C/T]ATCAAAATACACACA | 21888 |
rs38671483 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14460171 | AAAACAAAAACAGAG[C/T]CAAGGTCAATCAGGC | 21888 |
rs38673567 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14498056 | TGAATGCTTTCTCTA[C/T]TCTACCTTCTCCCTT | 21888 |
rs38684597 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Tle4 | GRCm38.p3 | 19:14559658 | ACACTTGATTGATTA[C/G]CATCAAGAATATGCT | 21888 |
rs38687455 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tle4 | Mm_Celera | 19:14468618 | CTGGCTGACAGAAAG[C/T]ATATATTTGAAATGC | 21888 |
rs38700023 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14455388 | ACACAATAACATTAC[C/T]TTTCAAGACATGGTG | 21888 |
rs38704943 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14492038 | CTTTTTATATAAAAT[C/T]ACATTATCATATGGT | 21888 |
rs38710173 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14495789 | TTAAGATGCTCTGAT[A/G]TTCTCCTCTGGCTTC | 21888 |
rs38714101 | snp | A/C/G | 0.277778 | 0.248452 | intron-variant | Tle4 | GRCm38.p3 | 19:14536701 | TTCAGGTTACCAACA[A/C/G]TTTGGAGAGAAGATA | 21888 |
rs38714335 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14502998 | GTACAGTTAGACTCT[G/T]TAAGCAAGCTGTAAA | 21888 |
rs38722303 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14585766 | AAAAATACTAATCAC[A/G]GAGGCTCAACTACAA | 21888 |
rs38724530 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14545393 | GCTTAAACAAACATG[C/T]AAATGAAATGGAAGT | 21888 |
rs38727431 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14478014 | AAGCCCAAAGTGATC[C/G/T]CCTTCTCTGCTGCAA | 21888 |
rs38729140 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14505310 | GATTATTTTTTCAGG[A/G]CAGCCCAATGAACTC | 21888 |
rs38744258 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Tle4 | Mm_Celera | 19:14589197 | ATTCCTCTTAACACA[C/T]ATACACACTCTAGTG | 21888 |
rs38744922 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14459788 | TTGAGCTGTTATTGA[A/T]TAATGCTGCTATTCC | 21888 |
rs38755654 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14580098 | ACAGAAGGATGTGCA[A/G]TCACATGGTAAGTAA | 21888 |
rs38787692 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14485051 | ATTTTGTTTTGTAAC[C/T]CAACTTCGTTATGGT | 21888 |
rs38799386 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Tle4 | Mm_Celera | 19:14530964 | GAAAATGGCATAATT[G/T]CAAGGAAAGAACTAT | 21888 |
rs38802931 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Tle4 | Mm_Celera | 19:14454520 | CTAGACTTCAGAAAG[A/T]TCTCAGGTATGAGTG | 21888 |
rs38803377 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14521166 | CATTACTAGAGATTT[C/T]TTATTCTTAGTATGT | 21888 |
rs38815368 | snp | C/G | 0.5 | 0 | intron-variant | Tle4 | Mm_Celera | 19:14467168 | CAGAAGTAGGGCTAG[C/G]TACTAACATACCTCA | 21888 |
rs38846168 | snp | A/G | 0.18 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14451617 | AGGCTCACAGGACAC[A/G]CGCTGCTCAGCAAGC | 21888 |
rs38851155 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14501585 | ATGCTGTCCTGTAAC[A/G]TGCATTGATAATTCC | 21888 |
rs38869519 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14569870 | GCTATGAATGCAGCC[C/T]AAGACATTTGCAGAT | 21888 |
rs38896555 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14588844 | CAATCCATTTCCTAA[C/G]AGGGCAGCCTCCTAG | 21888 |
rs38907417 | snp | C/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14565501 | CAATGCAATTAATAT[C/T]CCTGAGACATTAAAT | 21888 |
rs38936061 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14477474 | AAGCACCGGGGAAGG[C/T]TGAGAGGCACTCCTC | 21888 |
rs38953894 | snp | C/T | 0.277778 | 0.248452 | utr-variant-3-prime | Tle4 | GRCm38.p3 | 19:14449095 | TGTAATCTAAAGTTA[C/T]AGACATATTGGTTAA | 21888 |
rs38966757 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14488930 | TGATCATAGAAATAT[A/T]TTAAAAGGACATAAA | 21888 |
rs38977121 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14571326 | CTCGCTAGAATGCTA[G/T]ACTGGGAAAGCACTT | 21888 |
rs38980899 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Tle4 | Mm_Celera | 19:14541178 | ATGAGGAATTTTTTT[A/T]AAATACATTTTCTAT | 21888 |
rs38992057 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14458192 | CCTTCTTTGTGTCAG[C/T]ATGTGTGGAGATGGT | 21888 |
rs39000632 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Tle4 | Mm_Celera | 19:14497662 | AATTTTCATTCCTTA[C/T]GGGATCAATACACTA | 21888 |
rs39034475 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14570583 | ATGTGCCATAGAACA[C/T]ACAGACCTCAAGCAG | 21888 |
rs39040758 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tle4 | Mm_Celera | 19:14527705 | TACTCAGATTACTCA[C/T]ATCAAAAAGAGTAAG | 21888 |
rs39051996 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14452728 | CGCCAAGAAATACCT[A/C]ATGTAAGCACACTCT | 21888 |
rs39073625 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14519406 | GAGCAGAACTCCCTC[C/T]GTTAACCTAGCCTCG | 21888 |
rs39099191 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14524608 | TCTCACCATAAGAAC[A/T]GACCTAGATAGAACT | 21888 |
rs39127160 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tle4 | Mm_Celera | 19:14512955 | CTCAATATTGACGGA[A/G]TTTGTAAGAATACAA | 21888 |
rs39135934 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14572885 | GGATGAGTCTGGTTT[A/G]GATAGGATAGTCAAA | 21888 |
rs39172898 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Tle4 | GRCm38.p3 | 19:14568091 | AAGCAATGAGGAGCA[C/G]AACAGAGGATTCACC | 21888 |
rs39216335 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Tle4 | Mm_Celera | 19:14536921 | TCACTGCATCACAAA[A/G]ATTGAATTGCGACTA | 21888 |
rs39218208 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14487155 | ATGAAAGGAACAATG[C/G]TTCTTGTGTGAGTTT | 21888 |
rs39220847 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14557743 | AAGTCATACAAAGGC[A/G]AGACAAGAGTGGGAA | 21888 |
rs39243066 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14578974 | GCATAAGATTCAGTA[C/G]CAGGAGAAATGAAAA | 21888 |
rs39264928 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14491755 | TTATATAATCTAGGT[A/G]CATATCCCAGTTGTA | 21888 |
rs39270885 | snp | C/T | 0.18 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14451360 | ATGTATACATAAACA[C/T]GAAAATGCCACAGAA | 21888 |
rs39283101 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14518049 | CAGTAGGTGTACTAG[C/G]ATAAGGAAGCAGTCA | 21888 |
rs39322268 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14495380 | CCTAAAATTTTTGGT[C/T]AAAAGGGATGCAAAA | 21888 |
rs39331839 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Tle4 | Mm_Celera | 19:14556442 | CTAGTCTTTAACTGA[G/T]AAATACTTTAAAGAA | 21888 |
rs39338792 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14478209 | AACGCAGTGCTGTGA[A/C]TAGGGAGAATAACTA | 21888 |
rs39350373 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle4 | Mm_Celera | 19:14569090 | AATACAGAAAGGAGG[A/G]TGAGAGAGAAAAGTC | 21888 |
rs39378611 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14584616 | TGAGGCTTAAATTAG[A/C]GATGGACAAAGCAAA | 21888 |
rs39384431 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14493031 | AAAGAAAAAATTATA[A/T]CACTAAATAGCAGCA | 21888 |
rs39411638 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Tle4 | Mm_Celera | 19:14457937 | CTACCAGAGCCTGCT[A/G]AGGGGTTCCCAGCAA | 21888 |
rs39439292 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14569970 | ATCACCCTTTTTTTT[C/T]CACTAGATCTCCCTC | 21888 |
rs39485253 | snp | G/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14484491 | TTTCCTAAATCAGCA[G/T]CTGTACTGTAACTAA | 21888 |
rs39535402 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14460346 | TCTTTGAATAAACTT[G/T]TACTATGAGTATCAA | 21888 |
rs39614506 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14477593 | CCTCAACCTGTGAGA[C/T]GAGGCCAGGACCTGC | 21888 |
rs39783511 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tle4 | Mm_Celera | 19:14506022 | GCAATACGCATATAG[C/T]TTTGACCACCCTCTG | 21888 |
rs39809118 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14575352 | TGTGAAAACACAGTG[C/G]ATACACATCTTCAGC | 21888 |
rs39813965 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Tle4 | GRCm38.p3 | 19:14542693 | TTCGGATGCCCAGAA[C/T]GGCTCCGCTCACTTT | 21888 |
rs39839884 | snp | A/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Tle4, Gm31441 | Mm_Celera | 19:14562922 | CTGTTTTCCAGCACT[A/T]CTTCTGGCTTCTGTC | 21888 |
rs40022784 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Tle4 | Mm_Celera | 19:14579475 | CTACTACTAAACAAG[A/C/G]CTGGAAATGGTGACC | 21888 |
rs40064731 | snp | C/T | 0.32 | 0.24 | intron-variant | Tle4 | Mm_Celera | 19:14493590 | GGGTTCATCACAAAG[C/T]GAGAGTCAGGAGACA | 21888 |
rs40304060 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Tle4 | Mm_Celera | 19:14451260 | ACGCTTAGAAAAAAG[A/G]AGTGGTAACAGAAAG | 21888 |
rs46266397 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14552895 | CTCTTTTCACATCAC[A/G]TTCTATCTGAGACAA | 21888 |
rs46619090 | snp | C/T | | | intron-variant | Tle4 | GRCm38.p3 | 19:14468121 | ACGACAAACCAGCCT[C/T]CCCAAAGCAATGGTG | 21888 |
rs46761667 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14511208 | ACACAAAATATAAGA[C/T]TAAATTGCAAAGAGC | 21888 |
rs47620505 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14591592 | CTAGAACATTCCACT[C/T]GAACTTCTCCGGATG | 21888 |
rs48295449 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14527883 | AGACCAGGTTGGCCT[C/T]GAACTCAGAAATCCG | 21888 |
rs48936200 | snp | A/C | | | intron-variant | Tle4 | GRCm38.p3 | 19:14450574 | CACTGAAGAGAGGTG[A/C]AGGGTGATGAAGGGA | 21888 |
rs49066417 | snp | A/C | | | intron-variant | Tle4 | GRCm38.p3 | 19:14475236 | AGCCTGTATAATAAG[A/C]CAACCCTCACTGGCA | 21888 |
rs49430025 | snp | C/T | | | intron-variant | Tle4 | GRCm38.p3 | 19:14539077 | CCATCCTGCCAGGAC[C/T]CTTTGAAGGATCAAT | 21888 |
rs49534074 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14511808 | AAGCAAGTTGGGGAG[A/G]AAAGGGTTTATTCAG | 21888 |
rs49892519 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14490180 | AATCTACCAAGAACT[C/T]TCAATTCTGAACATC | 21888 |
rs49980474 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14511838 | GCTTATACTTCCATA[C/T]TGCTGTTCATCACCA | 21888 |
rs50382731 | snp | A/C | | | intron-variant | Tle4 | Mm_Celera | 19:14511843 | TTCCTTGGTGATGAA[A/C]AGCCATGTGGAAGTG | 21888 |
rs50402648 | snp | A/C | | | intron-variant | Tle4 | GRCm38.p3 | 19:14525067 | CCCTGTCTCAAAAAA[A/C]CAAAAAACAAAACAA | 21888 |
rs50424690 | snp | A/T | | | intron-variant | Tle4 | Mm_Celera | 19:14511859 | TTCATCACCAAAGGA[A/T]GTCAGGACTGGAATT | 21888 |
rs50856223 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14553090 | GAAATCCCTATCCCA[A/G]CCCCACTTCCCCTGC | 21888 |
rs50931824 | snp | C/G | | | intron-variant | Tle4 | Mm_Celera | 19:14496934 | AACAAACTGATAAAG[C/G]TACAAGTTAAATGCT | 21888 |
rs50957003 | snp | C/G | | | intron-variant | Tle4 | GRCm38.p3 | 19:14581668 | GTACTACCCAGACTG[C/G]TGTTCCAGGGAGGCT | 21888 |
rs51310204 | snp | A/T | | | intron-variant | Tle4 | Mm_Celera | 19:14465234 | AATTACTTAAATTAA[A/T]AAAAAAAAAGAAGTA | 21888 |
rs52081802 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14553135 | TCCCCCACCCACCCA[C/T]TCCTGCCTCCCTGCC | 21888 |
rs52190613 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14553100 | TCCCAGCCCCACTTC[C/T]CCTGCTTCTGTGAGG | 21888 |
rs52197310 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14502134 | CCATACATACATACA[C/T]ACACACACACACACA | 21888 |
rs52377834 | snp | G/T | | | intron-variant | Tle4 | GRCm38.p3 | 19:14568044 | CCTTGACTCTGCCCC[G/T]GATACTAGATACCAT | 21888 |
rs52396711 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14568051 | TCTGCCCCTGATACT[A/G]GATACCATCATGCTA | 21888 |
rs52450160 | snp | A/C | | | intron-variant | Tle4 | Mm_Celera | 19:14490415 | ACCCTGTCTCGAAAA[A/C]CCAAAAAAAAAAAAA | 21888 |
rs108232124 | snp | G/T | | | intron-variant | Tle4 | Mm_Celera | 19:14483312 | AGGCAAAGGCAAGCA[G/T]AGCTTTGTGAGTTCG | 21888 |
rs108475619 | snp | A/C | | | intron-variant | Tle4 | Mm_Celera | 19:14474976 | AATAATCAAAATAAC[A/C]CCAAACCAGTGAGAT | 21888 |
rs108612871 | snp | G/T | | | intron-variant | Tle4 | Mm_Celera | 19:14482994 | CAGCCCCCGAATCCC[G/T]CTGGCTTCCTACTTC | 21888 |
rs108791202 | snp | A/C | | | intron-variant | Tle4 | GRCm38.p3 | 19:14502173 | CACATATATATATTC[A/C]CCCCCCCCCCCCCAT | 21888 |
rs108832520 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14502160 | ACACACACACACACA[C/T]ATATATATATTCCCC | 21888 |
rs108853412 | snp | A/C/T | | | intron-variant | Tle4 | GRCm38.p3 | 19:14502171 | CACACATATATATAT[A/C/T]CCCCCCCCCCCCCCC | 21888 |
rs211705179 | snp | A/T | | | intron-variant | Tle4 | Mm_Celera | 19:14452800 | AGGCATGAAGTAAAA[A/T]GTTCAAAGTGGGTCC | 21888 |
rs211721100 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14504940 | AGAGCAGGAAGAACT[A/G]TGCAGTCTGAAGAGC | 21888 |
rs211733277 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14517392 | TTAAGGATACATGTA[C/T]TTTAAACAAGATTTC | 21888 |
rs211795193 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14505990 | TGCAGCCCACCACAC[C/T]AGCACTGACCACCAA | 21888 |
rs211797710 | in-del | -/CTTAA | | | intron-variant | Tle4 | Mm_Celera | 19:14583784 | AGATAAGCAAGTATT[-/CTTAA]CTTCTAGCTCCCCCT | 21888 |
rs211819830 | snp | C/T | | | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14565260 | ACAATGCACATGATT[C/T]TCCTACCTCGCAACT | 21888 |
rs211852762 | snp | C/G | | | intron-variant | Tle4 | Mm_Celera | 19:14555560 | CTGAGAAGCTATGGA[C/G]AGACGACAACTTTAG | 21888 |
rs211861847 | in-del | -/TATAAGTATAGGTA | | | intron-variant | Tle4 | Mm_Celera | 19:14559070 | AAGTATAGGTATACC[-/TATAAGTATAGGTA]TATATAAGTATAGGT | 21888 |
rs211873204 | in-del | -/C | | | intron-variant | Tle4 | Mm_Celera | 19:14580173 | AAATACCAAAGAAAG[-/C]AGGGGAATTAAAAGT | 21888 |
rs211885532 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14546983 | GTATCGAATCCCCTG[C/T]AGGAGCTGGAGTTAC | 21888 |
rs211969034 | snp | G/T | | | intron-variant | Tle4 | Mm_Celera | 19:14489622 | ATACAGATTCTAAGA[G/T]AACACAAATCCCAGC | 21888 |
rs211988207 | in-del | -/CT | | | intron-variant | Tle4 | Mm_Celera | 19:14476951 | TTGAGATATCTTATA[-/CT]CTCTCTTCTTTAGAA | 21888 |
rs212060846 | in-del | -/G | | | intron-variant | Tle4 | Mm_Celera | 19:14528288 | TACACAGAGTATACA[-/G]GAGTATACAGGAGTA | 21888 |
rs212063934 | in-del | -/CC | | | intron-variant | Tle4 | Mm_Celera | 19:14595708 | TTAACGCGTATCCTT[-/CC]AACTCCAAATCCACG | 21888 |
rs212067884 | snp | A/C/G | | | intron-variant | Tle4 | GRCm38.p3 | 19:14522857 | GTGCTGGCACAACTG[A/C/G]TTGTTATCATGTAGA | 21888 |
rs212075317 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14537374 | TGTATGCTACAAATT[A/G]CACTGTTTTACTACA | 21888 |
rs212082404 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14537857 | TAAATTTCTTTATGA[C/T]TTATAATCAGTAAAT | 21888 |
rs212108039 | snp | A/T | | | intron-variant | Tle4 | Mm_Celera | 19:14529870 | AGATCAAACCAATTA[A/T]GTAGAGCAGGAGAAA | 21888 |
rs212130090 | in-del | -/ATG | | | intron-variant | Tle4 | Mm_Celera | 19:14530615 | CTAGTGAAAATACTA[-/ATG]ATACTAATGATACTA | 21888 |
rs212135940 | snp | G/T | | | intron-variant | Tle4 | Mm_Celera | 19:14589735 | GGTGTATGCTACCAC[G/T]CCCAACAGTAGATTA | 21888 |
rs212142396 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14471940 | ACCAACTTCATCTGC[C/T]CTGGGCTTCTCAGAG | 21888 |
rs212151826 | snp | G/T | | | intron-variant | Tle4 | Mm_Celera | 19:14481498 | ATTCAGCCCAAATGC[G/T]TACAAATACCCTGAT | 21888 |
rs212171375 | in-del | -/T | | | intron-variant | Tle4 | Mm_Celera | 19:14461477 | CAGTGGGCGTGCAAC[-/T]TTTTGACTAAAGGTA | 21888 |
rs212193568 | snp | G/T | | | intron-variant | Tle4 | Mm_Celera | 19:14463724 | TTTTTTTTTGAGATT[G/T]AAATACTAGTCTGAA | 21888 |
rs212201014 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14590082 | AAGTGCTATCCTCAA[A/G]TAAATTGACTGCACC | 21888 |
rs212236902 | snp | A/G | | | synonymous-codon | Tle4 | GRCm38.p3 | 19:14464789 | CGCAGCTGCAGCAGC[A/G]GCTGCACTCATCTGG | 21888 |
rs212238738 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14454266 | CGGCCTAGCATTGTT[A/G]TGTCTGACTGACAGG | 21888 |
rs212279909 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14519752 | ATACACACATATACA[C/T]ACCTGTGCACATATA | 21888 |
rs212307183 | snp | G/T | | | intron-variant | Tle4 | Mm_Celera | 19:14510228 | AGCCTAATGACCTCC[G/T]GAGTTCAAGTCCTGA | 21888 |
rs212314668 | in-del | -/TGA | | | intron-variant | Tle4 | Mm_Celera | 19:14575077 | CAAGAAGCCAAGAGT[-/TGA]CTCTAGCACAAAAGT | 21888 |
rs212319924 | in-del | -/GGGGGGGCGCGC | | | intron-variant | Tle4 | GRCm38.p3 | 19:14554108 | GGGGGGGGGGGGGGG[-/GGGGGGGCGCGC]GGACCTGAGATTCCA | 21888 |
rs212347679 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14499801 | TCCCCCACAGCCTCA[C/T]ACATTTCTAGTTTGT | 21888 |
rs212374658 | in-del | -/GC | | | intron-variant | Tle4 | Mm_Celera | 19:14576679 | TCCTGGCTTAGAGGA[-/GC]GCTAAATGGCCATAG | 21888 |
rs212374846 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14499230 | AATCAGTAAGTAGTA[C/T]AGTGCAGAGATGTGT | 21888 |
rs212382893 | snp | C/T | | | intron-variant, downstream-variant-500B | Tle4, Gm31441 | Mm_Celera | 19:14567221 | CATGGTTAATCAGGA[C/T]TCTAATCTGCTATCC | 21888 |
rs212418888 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14557951 | CTACTGTCCAAACAC[C/T]TTTAATCCCAGCACT | 21888 |
rs212421139 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14491192 | TCCTGGGGATCTATC[C/T]CACATACAGTCATCA | 21888 |
rs212444957 | snp | A/T | | | intron-variant | Tle4 | Mm_Celera | 19:14486301 | AAAAAAAAAAAAAAA[A/T]TAACCAGTGAAAGAA | 21888 |
rs212499768 | in-del | -/AC | | | intron-variant | Tle4 | Mm_Celera | 19:14502130 | TAACCATACATACAT[-/AC]ACATACACACACACA | 21888 |
rs212551202 | in-del | -/AAT | | | intron-variant | Tle4 | Mm_Celera | 19:14583243 | TCAAAAAAACCAAAA[-/AAT]CAAAAAACAAAAACC | 21888 |
rs212562403 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14508793 | ATGCATTCTAATTAA[A/G]AAATTAGAGATAATA | 21888 |
rs212575458 | in-del | -/GAGGTAAT | | | intron-variant | Tle4 | Mm_Celera | 19:14494116 | GGCATGCATATTGTA[-/GAGGTAAT]GATGGGCAAACACAA | 21888 |
rs212588823 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14550732 | CCAGTTCAGATGATG[A/G]ATACATACACATAGC | 21888 |
rs212598952 | snp | A/C | | | intron-variant | Tle4 | Mm_Celera | 19:14592278 | AATAAGTGAATAAGC[A/C]TAAACCGATCTTGAG | 21888 |
rs212611740 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14474213 | ACTGGCCAGGAAGAA[C/T]GACGCTGCAACAGGA | 21888 |
rs212630662 | in-del | -/T | | | intron-variant, nc-transcript-variant | Tle4, Gm31441 | Mm_Celera | 19:14565112 | TTCAAACAGTAAAGG[-/T]TTCTAACTGTCAGCT | 21888 |
rs212638759 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14484431 | CCTAGCATATGCAAC[A/G]GGGGAGGAGGAGGAA | 21888 |
rs212639546 | in-del | -/A | | | intron-variant | Tle4 | Mm_Celera | 19:14572452 | TTTAGGAAAGAAGAC[-/A]AAAAAAAAACCAAAA | 21888 |
rs212657023 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14465842 | AAGATAACCAGAGTT[C/T]CAGAAGGAAGGACAG | 21888 |
rs212660957 | snp | A/C | | | intron-variant | Tle4 | Mm_Celera | 19:14592888 | AAACAAAAGTATTTA[A/C]AAGATCCAGACTGTA | 21888 |
rs212673144 | in-del | -/GT | | | intron-variant | Tle4 | Mm_Celera | 19:14495118 | AGACTAATTCTTGGG[-/GT]GGGGGGGCAAAATAG | 21888 |
rs212696290 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14531692 | AACATAAACATTCTG[C/T]GTACATATATTCCAT | 21888 |
rs212734595 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14532380 | ATAACTAAAGTAAAA[A/G]GGAGCCTAAATTTTA | 21888 |
rs212750070 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14466121 | GCAGCTTGCTGGCAA[A/G]TTCAGTCAGGCATTC | 21888 |
rs212770379 | snp | A/T | | | intron-variant | Tle4 | Mm_Celera | 19:14522077 | ATGACATTGAATCTT[A/T]AGATTGCTTTTGGCA | 21888 |
rs212781030 | in-del | -/TGTACAAC | | | intron-variant | Tle4 | Mm_Celera | 19:14594679 | GCAGCATTCTTAACT[-/TGTACAAC]TGTCTTTCTACATCA | 21888 |
rs212790127 | snp | A/T | | | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14549818 | TAGAAAGTGAGACAT[A/T]ATGAAAATGTTTTAA | 21888 |
rs212805735 | snp | G/T | | | intron-variant | Tle4 | Mm_Celera | 19:14584440 | ATTTTAATCTACATA[G/T]TTGACTACAGCTGCT | 21888 |
rs212828241 | in-del | -/T | | | intron-variant | Tle4 | Mm_Celera | 19:14488179 | AGACAAAGCACACGA[-/T]TTTTTTACAAAGCTA | 21888 |
rs212828611 | snp | A/C | | | intron-variant | Tle4 | Mm_Celera | 19:14577333 | CCTGCTAGTTACTAG[A/C]CTGGGGCAGAGACGA | 21888 |
rs212830221 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14457310 | CTGCAGAGGAAAGGG[C/T]CACATCAGGGAAGCC | 21888 |
rs212862304 | snp | A/C | | | intron-variant | Tle4 | Mm_Celera | 19:14457931 | GTCTGTCTACCAGAG[A/C]CTGCTGAGGGGTTCC | 21888 |
rs212877095 | in-del | -/TAT | | | intron-variant | Tle4 | Mm_Celera | 19:14577221 | CCACAATGAAAAAGG[-/TAT]TTGAAAGTCATGCGT | 21888 |
rs212882273 | snp | A/T | | | intron-variant | Tle4 | Mm_Celera | 19:14512861 | GCATACACACAGAAA[A/T]GCATTTAGTGTGAAA | 21888 |
rs212898654 | in-del | -/T | | | intron-variant | Tle4 | Mm_Celera | 19:14576832 | TTGCTACTTCATAAC[-/T]TTTTTTTGCTACTGT | 21888 |
rs212901563 | snp | A/T | | | downstream-variant-500B | Tle4 | Mm_Celera | 19:14447728 | TGAGGTCCAGTACAA[A/T]AGCTGTTAGCTCCTG | 21888 |
rs212902262 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14524638 | TACAGCCAGCATTAG[A/G]TACCATCTTCTTTAA | 21888 |
rs212902973 | in-del | -/A | | | intron-variant | Tle4, Gm31441 | Mm_Celera | 19:14566010 | CAGAATAGAACTCAG[-/A]AGGCTGAATGCTCAG | 21888 |
rs212949294 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14473201 | TTTAATTCAGAAAAG[C/T]CATGGTTTTGCTGTA | 21888 |
rs212970408 | snp | C/G | | | intron-variant | Tle4 | Mm_Celera | 19:14539646 | TCTCAGGCAAAATCC[C/G]CTAGAAACTTGAATT | 21888 |
rs213009208 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14493653 | CATATAAATCAAAGA[A/G]CATCATCTGTGGACC | 21888 |
rs213027776 | in-del | -/C | | | intron-variant | Tle4 | Mm_Celera | 19:14498096 | CCACTCTCACACACA[-/C]CCCCCCCCCGCCCCC | 21888 |
rs213120097 | snp | A/T | | | intron-variant | Tle4 | Mm_Celera | 19:14552685 | ACCACTGTATTATTT[A/T]GTTCCTTTCCGCCCT | 21888 |
rs213139805 | in-del | -/GCCCCCTGATC | | | intron-variant | Tle4 | Mm_Celera | 19:14457900 | AGCTGCTAAACCATA[-/GCCCCCTGATC]CCAATGTGGCAAGAC | 21888 |
rs213157538 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14494368 | ATACAAAGCATAAGG[C/T]CTGAAGATCCATGGT | 21888 |
rs213187046 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14477221 | TTCCTTAGAGGATAC[A/G]CCTAAGCCTTTTCAC | 21888 |
rs213192939 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14485898 | GTAATAAACTCAAAG[C/T]TTTGGTAAGCATGTG | 21888 |
rs213214573 | snp | G/T | | | intron-variant | Tle4 | Mm_Celera | 19:14595329 | CTTTTTTCCACTTTT[G/T]TAAAAATCTGTAAAA | 21888 |
rs213239969 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14468070 | TGTGTTCTAAAATTG[C/T]CTGATAATGGTTAAA | 21888 |
rs213257401 | snp | A/C | | | intron-variant | Tle4 | Mm_Celera | 19:14534434 | CATGGTATCTTTTCA[A/C]AGCAATGGAAACCCT | 21888 |
rs213267084 | in-del | -/CT | | | intron-variant | Tle4 | Mm_Celera | 19:14462074 | TGGAAAATACACCCC[-/CT]GATACAACAGAGACA | 21888 |
rs213272890 | snp | A/C | | | intron-variant | Tle4 | Mm_Celera | 19:14585203 | TCGAAAAACCAAAAC[A/C]AAAAAAAAAAAAAAA | 21888 |
rs213274964 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14596111 | GGTCTCCTGACAAAT[C/T]GTTTTTCCCCCTCCA | 21888 |
rs213288058 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14511814 | ATTAGGGAGGGAAGG[A/G]TTTATTCAGCTTACA | 21888 |
rs213334791 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14500828 | ATACTTTCTGACTAC[A/G]ATTTCTTAAGATTTG | 21888 |
rs213338341 | snp | G/T | | | intron-variant | Tle4 | Mm_Celera | 19:14489929 | GACTCAATTCCCCTA[G/T]AAAAAAAGACAGAGT | 21888 |
rs213346982 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14499109 | CCCAAGCACCCTAAA[C/T]GCTGCAAAAGGCCCC | 21888 |
rs213444299 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14472163 | CCAATGGCTAATAAT[A/G]ATAGGGTTTCAATGA | 21888 |
rs213474268 | snp | A/T | | | intron-variant | Tle4 | Mm_Celera | 19:14538635 | TGACCAAGTTGAAAT[A/T]GCAATCTCTGAGAAA | 21888 |
rs213493648 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14483300 | CCAGCACTCTGCAGG[C/T]AAAGGCAAGCATAGC | 21888 |
rs213508830 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14539350 | TATGTTTTGGCTTTT[A/G]TTAAAAAAGTAAAGT | 21888 |
rs213521220 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tle4 | Mm_Celera | 19:14549594 | CCAAAGGACAGGCAG[A/G]GTAGGATATATAGGG | 21888 |
rs213534608 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14542646 | CAGAACTGGTCACAT[A/G]AGTTTGTGACCAGGT | 21888 |
rs213540104 | snp | A/C | | | intron-variant | Tle4 | Mm_Celera | 19:14531535 | AAGATATGATGCAGT[A/C]ATGTGAATAACAGTA | 21888 |
rs213550985 | in-del | -/GGGGGTGA | | | intron-variant | Tle4 | Mm_Celera | 19:14533009 | ATCAACTGTTAAATT[-/GGGGGTGA]GGGGGTGGGGGGGAG | 21888 |
rs213554881 | in-del | -/A | | | intron-variant | Tle4 | Mm_Celera | 19:14510652 | TGAAAATCAACAATT[-/A]AAAAAATTGTACAGT | 21888 |
rs213570403 | snp | A/T | | | intron-variant | Tle4 | Mm_Celera | 19:14473036 | CTTCACAAACACGAA[A/T]GTTTTGCCTGAGGGT | 21888 |
rs213570631 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14465153 | TGCTTGGTTTGGAAT[A/G]CTTGCCTTCTCTAAC | 21888 |
rs213599570 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14590968 | TGTAAGTTGCATGCT[C/T]AGATTTTAAGTGTCA | 21888 |
rs213606752 | in-del | -/G | | | intron-variant | Tle4 | Mm_Celera | 19:14528417 | TATACAGAGTATACA[-/G]GAGTACACAGGAGTA | 21888 |
rs213631444 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14476260 | GTTAAGTAGAACTGG[C/T]TTAAGAACTATCTTG | 21888 |
rs213640943 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14466095 | ATACAGGAGACGGCG[C/T]AGGGAAAGATGCAGC | 21888 |
rs213658891 | in-del | -/TGTGTGTGTGTGTGTG | | | intron-variant | Tle4 | Mm_Celera | 19:14593527 | AAATAGCATTTTACA[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 21888 |
rs213668227 | snp | A/G | | | intron-variant | Tle4 | Mm_Celera | 19:14532192 | TTACTTCTAGATTCC[A/G]AGTTGTGTTTCATTA | 21888 |
rs213746624 | snp | C/T | | | intron-variant | Tle4 | Mm_Celera | 19:14500017 | GCTTCCTCATTTACA[C/T]CCTGACACATGCACA | 21888 |