SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1253 | snp | A/G | 0.133435 | 0.221162 | intron-variant | TLE1 | GRCh38.p7 | 9:81664878 | GGCCTGAGAATATTC[A/G]TTTCTAACAAGTTCC | 7088 |
rs2591 | snp | C/T | 0.198324 | 0.244601 | intron-variant | TLE1 | GRCh38.p7 | 9:81673438 | TTTGCAAAAACAAAA[C/T]GGAAGTATCAGTGAA | 7088 |
rs8782 | snp | C/T | 0.380121 | 0.213468 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590945 | CCTGGCGGCTCCAAC[C/T]CCGCGCATCAAGGCG | 7088 |
rs10420 | snp | A/C | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584003 | CCTGTCTACATAGAC[A/C]AAATGGAGCACCAAG | 7088 |
rs747151 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81655757 | GGATTTCTACTTTGT[C/G]TTTTTCCATTCTCTA | 7088 |
rs753484 | snp | A/G | 0.366885 | 0.220993 | intron-variant | TLE1 | GRCh38.p7 | 9:81673244 | CGCCATTGCACTCCA[A/G]CCTGGGGGACAAGAG | 7088 |
rs815843 | snp | A/G | 0.122411 | 0.214991 | intron-variant | TLE1 | GRCh38.p7 | 9:81626393 | GCAGGGTGATGGCTT[A/G]ATTGACACCAGGTGT | 7088 |
rs815844 | snp | C/T | 0.142609 | 0.225759 | intron-variant | TLE1 | GRCh38.p7 | 9:81601890 | CAGGAAACAAATGTT[C/T]GTTGCCTTGAATAGG | 7088 |
rs815845 | snp | G/T | 0.275999 | 0.248644 | intron-variant | TLE1 | GRCh38.p7 | 9:81601175 | TGTTTTTGTCTAGAT[G/T]CCACAGCTCGCTTAT | 7088 |
rs815846 | snp | C/T | 0.402806 | 0.197864 | intron-variant | TLE1 | GRCh38.p7 | 9:81607990 | GCTTTTTAGGAAAGC[C/T]GATTCCCATTGCTCT | 7088 |
rs815847 | snp | A/G | 0.5 | 0.00019968 | intron-variant | TLE1 | GRCh38.p7 | 9:81607703 | AGATAGGAAATGCTC[A/G]CAAGTGCCCCAAGGA | 7088 |
rs815848 | snp | A/G | 0.290201 | 0.246747 | intron-variant | TLE1 | GRCh38.p7 | 9:81607021 | GCCTAGGCTGGTTTC[A/G]AACTCCTGGGCTCAA | 7088 |
rs815849 | snp | A/C | 0.0829062 | 0.185956 | intron-variant | TLE1 | GRCh38.p7 | 9:81606802 | ACTGCCTCTCTCTCT[A/C]TATATATATATATGG | 7088 |
rs815850 | snp | G/T | 0.301932 | 0.244547 | intron-variant | TLE1 | GRCh38.p7 | 9:81606787 | ATATATATATATATG[G/T]ttttttttttaatta | 7088 |
rs815851 | snp | A/G | 0.395087 | 0.203592 | intron-variant | TLE1 | GRCh38.p7 | 9:81606417 | AGTATTCCATGGTGT[A/G]TATGTGCCACATTTT | 7088 |
rs815852 | snp | C/G | 0.249886 | 0.25 | intron-variant | TLE1 | GRCh38.p7 | 9:81606164 | acagtcccatcaaca[C/G]tgtaaaagtgttctt | 7088 |
rs815853 | snp | C/T | 0.256897 | 0.249905 | intron-variant | TLE1 | GRCh38.p7 | 9:81605785 | cgtgcagaaactctt[C/T]agtttaattagatcc | 7088 |
rs815854 | snp | A/T | 0.298651 | 0.24522 | intron-variant | TLE1 | GRCh38.p7 | 9:81604642 | GCCTCGTGCAGTGAC[A/T]GTGTGCCTCTGACCG | 7088 |
rs815855 | snp | A/C | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583878 | GATCACGCCTTGCCC[A/C]AGTGTGAGATTACCT | 7088 |
rs815857 | snp | C/T | 0.428937 | 0.17459 | intron-variant | TLE1 | GRCh38.p7 | 9:81595798 | AGACAGAGTCTCTGT[C/T]GCCCAGGCTGGAGTG | 7088 |
rs815858 | snp | A/G | 0.163892 | 0.234703 | intron-variant | TLE1 | GRCh38.p7 | 9:81595750 | ctcaccacaagctcc[A/G]cctcccaggttcacg | 7088 |
rs815859 | snp | A/G | 0.163236 | 0.234461 | intron-variant | TLE1 | GRCh38.p7 | 9:81595556 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 7088 |
rs815860 | snp | A/G | 0.278664 | 0.248351 | intron-variant | TLE1 | GRCh38.p7 | 9:81594634 | CACTTATTGTTTATG[A/G]TTTGAACTTCTAGCT | 7088 |
rs815861 | snp | A/T | 0.293551 | 0.246177 | intron-variant | TLE1 | GRCh38.p7 | 9:81593782 | GAAAGTTGAAGTCCA[A/T]ACCATAAACTGGTAT | 7088 |
rs843816 | snp | C/T | 0.183568 | 0.241012 | intron-variant | TLE1 | GRCh38.p7 | 9:81604701 | AGGGACCTTAATGTC[C/T]CTTTAGTATAAATGC | 7088 |
rs864179 | snp | A/G | 0.36955 | 0.219562 | intron-variant | TLE1 | GRCh38.p7 | 9:81596905 | ATACCATACACATAC[A/G]GAAAAGTGCATGAAT | 7088 |
rs870713 | snp | A/C | 0.415399 | 0.187465 | intron-variant | TLE1 | GRCh38.p7 | 9:81612243 | AATTAAGAGTATTCC[A/C]TACCCAATTTACAGA | 7088 |
rs873755 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81612451 | CTGTTGCCTATTTTC[C/T]TTTGGGCCCAGGTTG | 7088 |
rs874754 | snp | C/T | 0.46014 | 0.13543 | intron-variant | TLE1 | GRCh38.p7 | 9:81635690 | TTTGCGTGCACTGAA[C/T]ATATTAAATCTTCAT | 7088 |
rs911638 | snp | A/G | 0.174932 | 0.238463 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589485 | ATAGAATGGGGTAGC[A/G]TCTTACAAATCTTTC | 7088 |
rs911639 | snp | C/T | 0.364609 | 0.222182 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589459 | CTTTCTCTGGACCAC[C/T]CACAGGTGGCTAGTG | 7088 |
rs944592 | snp | A/G | 0.439918 | 0.162576 | intron-variant | TLE1 | GRCh38.p7 | 9:81613140 | TTTTTTTCTTGAGAC[A/G]AAGTCTCGCTCTTGT | 7088 |
rs944593 | snp | C/G | 0.484421 | 0.0868729 | intron-variant | TLE1 | GRCh38.p7 | 9:81611625 | ACAAAGACGCCCAGT[C/G]TCCCAGCCACACACT | 7088 |
rs947672 | snp | A/T | 0.428786 | 0.174744 | intron-variant | TLE1 | GRCh38.p7 | 9:81640218 | AGAACATGAATTCTA[A/T]TTAATGGCACAGAAT | 7088 |
rs947673 | snp | A/C | 0.141258 | 0.225111 | intron-variant | TLE1 | GRCh38.p7 | 9:81640202 | TTAATGGCACAGAAT[A/C]TCAGCTTAGGTCTAA | 7088 |
rs1047377 | snp | A/C | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81633522 | AATTTTCAGGAAATC[A/C]CTGTATTAGGAATGT | 7088 |
rs1159642 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | TLE1 | GRCh38.p7 | 9:81658335 | TCCTCCTGTTTCAGG[A/C]TTATCCAGTCTAACC | 7088 |
rs1331865 | snp | A/G | 0.314301 | 0.241589 | intron-variant | TLE1 | GRCh38.p7 | 9:81624785 | TTTGTTTATTTGTTT[A/G]TTTTTTTAATTTTAA | 7088 |
rs1342477 | snp | C/T | 0.406296 | 0.19512 | intron-variant | TLE1 | GRCh38.p7 | 9:81632305 | TCCTTCAACCATTCC[C/T]CACTCCTCCACGCAC | 7088 |
rs1342478 | snp | A/G | 0.286825 | 0.247273 | intron-variant | TLE1 | GRCh38.p7 | 9:81632511 | TACCATATTAAACAC[A/G]GTCAAAATACTGCTA | 7088 |
rs1385041 | snp | A/C | 0.230603 | 0.249246 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690747 | GGTTTTTCAGGTCTC[A/C]GTGCTGGTTTATTAC | 7088 |
rs1385042 | snp | C/T | 0 | 0 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687360 | GATTAAAGAGGAATT[C/T]CAGTTCCTGCAGGCG | 7088 |
rs1484112 | snp | C/T | 0.0562307 | 0.157967 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691199 | GTCTGTTTAAATAAG[C/T]TCCTTCCCGTAAGTC | 7088 |
rs1484113 | snp | A/C | 0.316726 | 0.240931 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690817 | CCCATTTAGCTCTTC[A/C]CACAGCTCAGCTCAG | 7088 |
rs1539375 | snp | A/G | 0.435837 | 0.167226 | intron-variant | TLE1 | GRCh38.p7 | 9:81607079 | aaaaaaaaaaaaTGG[A/G]GAGAGAGAGAGATTT | 7088 |
rs1539377 | snp | A/T | 0.455144 | 0.142885 | intron-variant | TLE1 | GRCh38.p7 | 9:81597507 | CTATCCAAACGTCCA[A/T]CTCTACTCTTTGGGC | 7088 |
rs1573077 | snp | A/T | 0.392325 | 0.205532 | intron-variant | TLE1 | GRCh38.p7 | 9:81597748 | TTAATGGGTTTTTAT[A/T]TCATTCATGTTTTAC | 7088 |
rs1573078 | snp | G/T | 0.457737 | 0.139088 | intron-variant | TLE1 | GRCh38.p7 | 9:81597621 | TAGGTGGGGGCTGGG[G/T]CTCAGTTCTGAGGCT | 7088 |
rs1804529 | snp | C/T | 0 | 0 | missense | TLE1 | GRCh38.p7 | 9:81593251 | CCTTCCACGTTACTG[C/T]AGACGGTCAGATGCA | 7088 |
rs1804530 | snp | G/T | | | missense | TLE1 | GRCh38.p7 | 9:81616660 | GACAACTTAGTTGTG[G/T]ATGTGTCTAATGAGG | 7088 |
rs1804531 | snp | A/G/T | 1.65097e-05 | 0.00287308 | synonymous-codon, missense | TLE1 | GRCh38.p7 | 9:81593037 | GAGCCCTGTCTCCCA[A/G/T]CTCGACTGTCTGAAC | 7088 |
rs1872196 | snp | A/G | 0.195837 | 0.244062 | intron-variant | TLE1 | GRCh38.p7 | 9:81673222 | AGGTTGCAGTGAACC[A/G]AGATTGCGCCATTGC | 7088 |
rs1888812 | snp | C/T | 0.471863 | 0.115225 | | | GRCh38.p7 | 9:81621814 | ATTGCCTTCCGGTCC[C/T]CAGTTTTGATTTCCT | 7088 |
rs2004967 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | TLE1 | GRCh38.p7 | 9:81673642 | ATCCCACTCACCTGT[C/T]TTCTCTTTTTCAAGG | 7088 |
rs2018988 | snp | A/T | 0.197703 | 0.244469 | intron-variant | TLE1 | GRCh38.p7 | 9:81636855 | CCACCACACCTGGCT[A/T]ATTGTTGTATTTTTA | 7088 |
rs2129105 | snp | C/T | 0.317451 | 0.240729 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687574 | CCCCATAGTGAAGGG[C/T]AAACTCGAGTTTGGG | 7088 |
rs2129106 | snp | A/C | 0.27278 | 0.24896 | intron-variant | TLE1 | GRCh38.p7 | 9:81679510 | ACCTCACGGGGAAAA[A/C]AAATCAGAAAACCTC | 7088 |
rs2228172 | snp | A/G | 0.109578 | 0.206837 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585614 | CGGGGAGTGGCTGGC[A/G]GTGGGCATGGAGAGC | 7088 |
rs2228173 | snp | A/G | 0.166621 | 0.235686 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81652232 | GGTGACCATGGCAGA[A/G]TTGAATGCCATCATC | 7088 |
rs2229270 | snp | C/T | 4.96307e-05 | 0.00498125 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585629 | GGGGTACTGCCCCAC[C/T]GGGGAGTGGCTGGCA | 7088 |
rs2244337 | snp | G/T | 0.324855 | 0.23853 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685779 | ATATTAGCAAACGTG[G/T]TAGCAGAGTGTAAAA | 7088 |
rs2244732 | snp | C/T | 0.316726 | 0.240931 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688527 | AGCGCTGCCCCCGCG[C/T]ACAGTCCCCGAGCGC | 7088 |
rs2265659 | snp | A/G | 0.409721 | 0.192325 | intron-variant | TLE1 | GRCh38.p7 | 9:81657927 | GCGAGACTCTGTCTT[A/G]AAAAAAAAAAAAAAA | 7088 |
rs2277162 | snp | C/T | 0.363985 | 0.222503 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690785 | CACACCCCACCCCCA[C/T]AGTCTGGGTGGTACT | 7088 |
rs2279353 | snp | C/T | 0.161267 | 0.233723 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688111 | GGCGGACCTTCTCGC[C/T]CTCAGCGGTGTAAGG | 7088 |
rs2291300 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685783 | TATGATATTAGCAAA[C/T]GTGTTAGCAGAGTGT | 7088 |
rs2310105 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675872 | cgcccagctaatttt[A/C]gtattttcagcagag | 7088 |
rs2378591 | snp | G/T | 0.390277 | 0.206936 | intron-variant | TLE1 | GRCh38.p7 | 9:81638512 | TCCTTTGTTGAAGGT[G/T]ATAAGTACAAGATTG | 7088 |
rs2488274 | snp | C/G | 0.275197 | 0.248727 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689743 | CGCTGCGCTGCCATA[C/G]GCTCCGGGGAGGAGC | 7088 |
rs2506124 | snp | A/G | 0.322007 | 0.239405 | intron-variant | TLE1 | GRCh38.p7 | 9:81685443 | TGGAAATATAAACTA[A/G]CCTCTTTATTGACAG | 7088 |
rs2506125 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | TLE1 | GRCh38.p7 | 9:81678538 | gcgtgagccactgct[C/T]ccagccCCTAAATTT | 7088 |
rs2627002 | snp | G/T | 0.172997 | 0.237846 | intron-variant | TLE1 | GRCh38.p7 | 9:81660099 | TTGAGAAGGCTTTTA[G/T]GTAGAAAGCTGTTAA | 7088 |
rs2627003 | snp | G/T | 0.499816 | 0.0095829 | intron-variant | TLE1 | GRCh38.p7 | 9:81659007 | GAAGGAGAATTGCTT[G/T]AACCAGGGAGTCGGA | 7088 |
rs2627004 | snp | G/T | 0.180383 | 0.240111 | intron-variant | TLE1 | GRCh38.p7 | 9:81658524 | AAGCTGGCTTGTCAG[G/T]ATAGTTTAAGATTAG | 7088 |
rs2627005 | snp | A/G | 0.420733 | 0.18262 | intron-variant | TLE1 | GRCh38.p7 | 9:81652826 | ATCAACGGATTTAAT[A/G]TTAAAGTTTTAGGTA | 7088 |
rs2627007 | snp | C/G | 0.420255 | 0.183066 | intron-variant | TLE1 | GRCh38.p7 | 9:81651297 | GTTCGTCCCCTTCCA[C/G]ACTAAGCCAAAGAAG | 7088 |
rs2627008 | snp | A/C | 0.428937 | 0.17459 | intron-variant | TLE1 | GRCh38.p7 | 9:81649968 | TGGATTAGTATATGA[A/C]TTTATGTCCGAAGGC | 7088 |
rs2627009 | snp | C/T | 0.175897 | 0.238765 | intron-variant | TLE1 | GRCh38.p7 | 9:81649349 | CCTGTGGGTGCTCTT[C/T]GAGGAGACAGAGAGA | 7088 |
rs2627010 | snp | A/C | 0.428786 | 0.174744 | intron-variant | TLE1 | GRCh38.p7 | 9:81649347 | TGTGGGTGCTCTTCG[A/C]GGAGACAGAGAGAGG | 7088 |
rs2627016 | snp | A/G | 0.321769 | 0.239477 | intron-variant | TLE1 | GRCh38.p7 | 9:81684521 | GGAGTTACAAAAGCA[A/G]AATTCAACTCTGAAA | 7088 |
rs2627017 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671624 | cactccaacctgggc[A/G]acagagtgagactcc | 7088 |
rs2627018 | snp | A/G | 0.413416 | 0.189196 | intron-variant | TLE1 | GRCh38.p7 | 9:81662951 | ttcctgggcttaagc[A/G]attctcatgcctcag | 7088 |
rs2777772 | snp | G/T | 0.180383 | 0.240111 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589417 | GACATTCAATAGGCT[G/T]TACATGGCCCTATTA | 7088 |
rs2777773 | snp | C/T | 0.151334 | 0.229706 | intron-variant | TLE1 | GRCh38.p7 | 9:81592230 | gggcgtggtggtggg[C/T]gcccgtagtcccagc | 7088 |
rs2777774 | snp | A/C | 0.268995 | 0.249277 | intron-variant | TLE1 | GRCh38.p7 | 9:81593432 | TTGAAGCATTTACTG[A/C]TGGTGCAAATTTAAA | 7088 |
rs2777775 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | TLE1 | GRCh38.p7 | 9:81597425 | TGAGGCAACAAAAAA[C/T]ACAAAATTCTTAAGT | 7088 |
rs2777776 | snp | A/G | 0.45692 | 0.1403 | intron-variant | TLE1 | GRCh38.p7 | 9:81598031 | AAACAATAATGAAGA[A/G]CCACAGACCCCAGAG | 7088 |
rs2777777 | snp | C/T | 0.459801 | 0.135955 | intron-variant | TLE1 | GRCh38.p7 | 9:81598245 | AAACTCCCAGCCACA[C/T]AGGACAACAGGCCAG | 7088 |
rs2777778 | snp | C/G | 0.193028 | 0.243422 | intron-variant | TLE1 | GRCh38.p7 | 9:81598381 | CCCTCTGCCTGCCAC[C/G]AACTCCCCAGCCTTG | 7088 |
rs2777779 | snp | C/G | 0.192401 | 0.243274 | intron-variant | TLE1 | GRCh38.p7 | 9:81598384 | TCTGCCTGCCACGAA[C/G]TCCCCAGCCTTGATG | 7088 |
rs2777780 | snp | C/G | 0.462582 | 0.131564 | intron-variant | TLE1 | GRCh38.p7 | 9:81598880 | CTGTGGCAGAAGCAA[C/G]CAGAGGTCACATGGA | 7088 |
rs2777781 | snp | A/T | 0.420266 | 0.183056 | intron-variant | TLE1 | GRCh38.p7 | 9:81600119 | AGGAACAAGGCTCCT[A/T]AACAGGACAAAGATA | 7088 |
rs2796442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671570 | gaatggcgtgaaccc[A/G]ggaggcggagcttgc | 7088 |
rs2796443 | snp | C/T | 0.455263 | 0.142713 | intron-variant | TLE1 | GRCh38.p7 | 9:81677392 | AACATGATGAAATCC[C/T]GTCTCTACTAAAAAT | 7088 |
rs2796444 | snp | A/G | 0.304438 | 0.244001 | intron-variant | TLE1 | GRCh38.p7 | 9:81680082 | TCAATTTGCACGCAC[A/G]AGGTGCTGGGTTCTG | 7088 |
rs2796446 | snp | C/T | 0.405429 | 0.195811 | intron-variant | TLE1 | GRCh38.p7 | 9:81664165 | AAAATGGTGGGATTA[C/T]AGGCATGAGCCACCA | 7088 |
rs2796447 | snp | A/G | 0.376288 | 0.215757 | intron-variant | TLE1 | GRCh38.p7 | 9:81653963 | TTTAACAGCTGAACA[A/G]TTTTACTTACTTCCT | 7088 |
rs2796448 | snp | A/C | 0.495855 | 0.045338 | intron-variant | TLE1 | GRCh38.p7 | 9:81655246 | GTGGGCGCCTGTAAT[A/C]CCAGCTACTCGGGAG | 7088 |
rs2796449 | snp | C/T | 0.175576 | 0.238665 | intron-variant | TLE1 | GRCh38.p7 | 9:81655485 | ACTCTACTTCTAGCC[C/T]AGGGAAGGGTCCACC | 7088 |
rs2796450 | snp | C/T | 0.179105 | 0.239737 | intron-variant | TLE1 | GRCh38.p7 | 9:81660180 | GACACATTTCTTTGC[C/T]GTACCTCCCCTACTA | 7088 |
rs2796457 | snp | C/T | 0.252983 | 0.249982 | intron-variant | TLE1 | GRCh38.p7 | 9:81584892 | AAAGGATTAAACATC[C/T]AACTTAAGTAAAATG | 7088 |
rs2796458 | snp | G/T | 0.48498 | 0.0853497 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586081 | ggagtgaagcggcgt[G/T]atctcggctcactgc | 7088 |
rs2796459 | snp | A/T | 0.170084 | 0.236883 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586473 | tatttgtacatccag[A/T]tacatctaaacattg | 7088 |
rs2796460 | snp | A/C | 0.11963 | 0.213316 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586679 | atggccaaataactt[A/C]aagctgagcgatggg | 7088 |
rs2796461 | snp | C/T | 0.254385 | 0.249962 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587113 | AAGTTGCCATTTATA[C/T]ATTATTTCAAAAGTC | 7088 |
rs2796462 | snp | A/G | 0.25634 | 0.24992 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587311 | AAGTTCTATTTATTT[A/G]GGAATCAAAAAATCA | 7088 |
rs2796463 | snp | C/G | 0.25634 | 0.24992 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588033 | CGATTGTCTTTCCCT[C/G]TTTTCCACGATCCAA | 7088 |
rs2796464 | snp | C/T | 0.171057 | 0.237209 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589329 | CTCTCTCCGTCCATA[C/T]ACTATACTCCAGCAT | 7088 |
rs2796465 | snp | A/G | 0.168135 | 0.236216 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589690 | GGACAGACGTTATGA[A/G]AACTAAGTGGAGGAA | 7088 |
rs2796466 | snp | G/T | 0.408188 | 0.193589 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589864 | ACTACCCAGCAAACA[G/T]AAGAGGAAAGTAACT | 7088 |
rs2796467 | snp | A/G | 0.286042 | 0.247388 | intron-variant | TLE1 | GRCh38.p7 | 9:81591307 | AACTATCTAGGTATG[A/G]GGTACAGGTGTACAC | 7088 |
rs2796468 | snp | G/T | 0.170408 | 0.236992 | intron-variant | TLE1 | GRCh38.p7 | 9:81591333 | TACACATAGTTCCCT[G/T]AGAAGAAACCACTTT | 7088 |
rs2796469 | snp | C/G | 0.290977 | 0.246619 | intron-variant | TLE1 | GRCh38.p7 | 9:81592022 | TCGGAGTCTGCTTAA[C/G]GCCAGTGGTATGTGC | 7088 |
rs2796470 | snp | A/G | 0.170408 | 0.236992 | intron-variant | TLE1 | GRCh38.p7 | 9:81592087 | AACATggccgggcgc[A/G]gtggctcacgcctat | 7088 |
rs2796471 | snp | A/G | 0.298905 | 0.24517 | intron-variant | TLE1 | GRCh38.p7 | 9:81592942 | TTCCTCATAATGGGA[A/G]TAAAACCCAGGCCCA | 7088 |
rs2796472 | snp | A/G | 0.039522 | 0.134904 | intron-variant | TLE1 | GRCh38.p7 | 9:81622475 | GTTTAATGATGTCAA[A/G]TGGTACTGTGAACGT | 7088 |
rs2989943 | snp | A/G | 0.265727 | 0.249505 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586427 | atgttactgtactga[A/G]tactgtaggcaactg | 7088 |
rs3024227 | in-del | -/TAAA | 0.340333 | 0.233109 | intron-variant | TLE1 | GRCh38.p7 | 9:81675331 | TATGTAAAGACTAAG[-/TAAA]TAATCAGTGGTTATA | 7088 |
rs3045544 | in-del | -/GT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652107 | TGTGTGTGTGTGTGT[-/GT]ATCTTAACGTTGACC | 7088 |
rs3063325 | in-del | -/GT | 0.503941 | 0.0313876 | intron-variant | TLE1 | GRCh38.p7 | 9:81607337 | TGTGTGTGTGTGTGT[-/GT]ATTAACAGGGTCAGT | 7088 |
rs3739581 | snp | A/G | 0.460477 | 0.134905 | intron-variant | TLE1 | GRCh38.p7 | 9:81674380 | GAGGAAACAAAGACT[A/G]TGCTCCTGAGGAGCA | 7088 |
rs3814532 | snp | G/T | 0.464416 | 0.128553 | intron-variant | TLE1 | GRCh38.p7 | 9:81637851 | TGGAACACATCTGAG[G/T]CAGGGAGGGTAGGTA | 7088 |
rs3814533 | snp | C/T | 0.179425 | 0.239831 | intron-variant | TLE1 | GRCh38.p7 | 9:81637892 | TACCCATTTCACAGA[C/T]GATACTGGCTCAAAG | 7088 |
rs3814534 | snp | A/G | 0.34437 | 0.231505 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690045 | GGGCGCGCGCTAGCG[A/G]GAGGGACTGGCGAGC | 7088 |
rs3814535 | snp | A/G | 0.369958 | 0.21934 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690070 | GCGAGCGTGCAGCCG[A/G]GGAAGCTGAGGGCTC | 7088 |
rs3824418 | snp | C/G | 0.458545 | 0.137872 | intron-variant | TLE1 | GRCh38.p7 | 9:81674475 | TCTGGTCCTTACCCC[C/G]TTACCACCCAAGGTC | 7088 |
rs3889626 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | TLE1 | GRCh38.p7 | 9:81674229 | GGGATTTGCAGTAAA[C/T]GTATTACAGAACACA | 7088 |
rs3894391 | snp | A/G | 0.324619 | 0.238604 | intron-variant | TLE1 | GRCh38.p7 | 9:81675060 | ATGTTATCAGTCTAA[A/G]CCAAGGTCGGTAGCT | 7088 |
rs3897745 | snp | C/T | 0.471673 | 0.115589 | intron-variant | TLE1 | GRCh38.p7 | 9:81601029 | ATTTGGAGGGATTGG[C/T]TCACACGACTGTGTA | 7088 |
rs4069934 | snp | C/T | 0.195837 | 0.244062 | intron-variant | TLE1 | GRCh38.p7 | 9:81673141 | AGCTGGGCATGGTGG[C/T]GCACGCCTGTAATCC | 7088 |
rs4563962 | snp | A/T | 0.203267 | 0.245593 | intron-variant | TLE1 | GRCh38.p7 | 9:81666962 | atttctacagaaaaa[A/T]tttaaaaattagccg | 7088 |
rs4588939 | snp | A/G | 0.429388 | 0.174127 | intron-variant | TLE1 | GRCh38.p7 | 9:81643086 | GTAGGGGAAAATGAG[A/G]AGCAATTGGTCAAAG | 7088 |
rs4595209 | snp | C/T | 0.174932 | 0.238463 | intron-variant | TLE1 | GRCh38.p7 | 9:81644669 | acagcaatgtgaata[C/T]gctaaaaaccacaga | 7088 |
rs4877220 | snp | A/G | 0.46703 | 0.124089 | intron-variant | TLE1 | GRCh38.p7 | 9:81623705 | TGCAGCACAAGAATC[A/G]CTTGAACCTGGGAGG | 7088 |
rs4877221 | snp | C/G | 0.163564 | 0.234582 | intron-variant | TLE1 | GRCh38.p7 | 9:81647980 | CAGTTAAAAAAACAA[C/G]CATCTTTATGGGCAG | 7088 |
rs4877664 | snp | C/G | 0.467744 | 0.122832 | intron-variant | TLE1 | GRCh38.p7 | 9:81604247 | TGAGCTCCCGGTGGG[C/G]TCCCCTATGCCTATG | 7088 |
rs4877665 | snp | A/C | 0.49334 | 0.057322 | intron-variant | TLE1 | GRCh38.p7 | 9:81622002 | CCACAGTGTTTGGGG[A/C]TGAAAGGTGAGCCGG | 7088 |
rs4877666 | snp | C/G | 0.139564 | 0.224285 | intron-variant | TLE1 | GRCh38.p7 | 9:81641265 | CTACGTAAACACGTG[C/G]AAAAGAGCTGTCTGG | 7088 |
rs4877667 | snp | A/G | 0.173643 | 0.238054 | intron-variant | TLE1 | GRCh38.p7 | 9:81641380 | AGGGTGATCAACAGG[A/G]AGAAACTGCTTATGG | 7088 |
rs4877668 | snp | C/T | 0.4231 | 0.180378 | intron-variant | TLE1 | GRCh38.p7 | 9:81641386 | ATCAACAGGAAGAAA[C/T]TGCTTATGGGGCCAA | 7088 |
rs4877669 | snp | A/G | 0.497558 | 0.0348586 | intron-variant | TLE1 | GRCh38.p7 | 9:81647570 | GGCACAACCACCACC[A/G]ACCAGGACTTGACCA | 7088 |
rs4877670 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661172 | AAAATACATATATAT[A/T]TATATATATGTATTT | 7088 |
rs4877671 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661174 | AATACATATATATTT[A/T]TATATATGTATTTTT | 7088 |
rs4877672 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661190 | TATATATGTATTTTT[A/T]TATATATATGTATTT | 7088 |
rs5898749 | in-del | -/AC/CA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607338 | ACACACACACACACA[-/AC/CA]TATAAGGAATAGGGT | 7088 |
rs5898750 | in-del | -/AAC | 0.498589 | 0.02652 | intron-variant | TLE1 | GRCh38.p7 | 9:81618027 | AAGACTCCGTCTCAA[-/AAC]AACAACAACAACAAC | 7088 |
rs5898752 | in-del | -/A | 0.3746 | 0.216737 | intron-variant | TLE1 | GRCh38.p7 | 9:81634479 | GAGGGAGGAAAGGGG[-/A]AAAAATGCGATTAGT | 7088 |
rs5898753 | in-del | -/C | 0.493293 | 0.0575177 | intron-variant | TLE1 | GRCh38.p7 | 9:81636828 | GCCAAGATGGTGAAA[-/C]CCCGTCTCTACTAAA | 7088 |
rs5898754 | in-del | -/A | 0.456568 | 0.140818 | intron-variant | TLE1 | GRCh38.p7 | 9:81655853 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 7088 |
rs5898755 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655869 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAACA | 7088 |
rs5898756 | in-del | -/A | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81673280 | AAAAAAAAAAAAAAA[-/A]CAGACTGCCAACAAG | 7088 |
rs6559629 | snp | A/G | 0.492871 | 0.0592773 | intron-variant | TLE1 | GRCh38.p7 | 9:81592445 | TCTCAGGCTCTGAGC[A/G]GACGTGGCTTAGGTA | 7088 |
rs6559630 | snp | G/T | 0.487113 | 0.0792303 | intron-variant | TLE1 | GRCh38.p7 | 9:81622323 | GGGGCACAGAGGCTG[G/T]GTGTGCTGACCAGTT | 7088 |
rs6559631 | snp | A/C | 0.430136 | 0.173352 | intron-variant | TLE1 | GRCh38.p7 | 9:81644607 | acggagtttctttac[A/C]gggtgacaaaaatgt | 7088 |
rs6559632 | snp | A/G | 0.493523 | 0.0565391 | intron-variant | TLE1 | GRCh38.p7 | 9:81671436 | cggatcacaaggtca[A/G]gagttcaagaccagc | 7088 |
rs7018589 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | TLE1 | GRCh38.p7 | 9:81669367 | GCTGTTTTCAAATCC[A/G]TGGCACAAGCCAGGA | 7088 |
rs7018978 | snp | A/G | 0.433236 | 0.170072 | intron-variant | TLE1 | GRCh38.p7 | 9:81599040 | GAGCCTCATTTCCCC[A/G]TTTTTACAATGTGCC | 7088 |
rs7019677 | snp | G/T | 0.202035 | 0.245356 | intron-variant | TLE1 | GRCh38.p7 | 9:81670911 | ccgtggctcatgctg[G/T]taatcccagcacttt | 7088 |
rs7019824 | snp | C/T | 0.188 | 0.24219 | intron-variant | TLE1 | GRCh38.p7 | 9:81592295 | ccccggaggcggagc[C/T]tgcagtgagccgaga | 7088 |
rs7021592 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | TLE1 | GRCh38.p7 | 9:81669616 | CACCTCCACCCTCCC[C/G]CCCCACACCAAAAGA | 7088 |
rs7021918 | snp | G/T | 0.450609 | 0.149185 | intron-variant | TLE1 | GRCh38.p7 | 9:81639588 | TTGTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTG | 7088 |
rs7023704 | snp | C/G | 0.419445 | 0.183816 | intron-variant | TLE1 | GRCh38.p7 | 9:81592983 | TCCTTATTGAATCTC[C/G]AGGGAGAAATTGCCC | 7088 |
rs7024180 | snp | C/T | 0.396 | 0.202938 | intron-variant | TLE1 | GRCh38.p7 | 9:81649184 | CTTATTTTTCTTAAA[C/T]ACCGGTACTCTATGT | 7088 |
rs7024675 | snp | C/G | 0.365232 | 0.22186 | intron-variant | TLE1 | GRCh38.p7 | 9:81681442 | GTAATCCCAACTACT[C/G]AGGAGGCTGAGGCAG | 7088 |
rs7025418 | snp | C/T | 0.392325 | 0.205532 | intron-variant | TLE1 | GRCh38.p7 | 9:81666997 | tggtggtgtggccta[C/T]agtcccagctactgg | 7088 |
rs7028280 | snp | A/G | 0.43088 | 0.172575 | intron-variant | TLE1 | GRCh38.p7 | 9:81659236 | CCTGCCCATGCTTCT[A/G]TTCTTGATTGGAGTG | 7088 |
rs7028704 | snp | C/T | 0.438386 | 0.164349 | intron-variant | TLE1 | GRCh38.p7 | 9:81615407 | TGTGTGGCAAGAACA[C/T]ATCCCCCAAGTAAGA | 7088 |
rs7029058 | snp | C/T | 0.490997 | 0.0664859 | intron-variant | TLE1 | GRCh38.p7 | 9:81618849 | ATCTTAGCTTTGTAC[C/T]GGACCCTTCTGCAAA | 7088 |
rs7029433 | snp | A/G | 0.447421 | 0.153379 | intron-variant | TLE1 | GRCh38.p7 | 9:81619165 | TGAAAGTACACAATG[A/G]AAGTACATGCATGGG | 7088 |
rs7029534 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81637709 | TAAGTAACAATCAAA[C/T]GGATCACAACTGCTG | 7088 |
rs7032210 | snp | G/T | | | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689660 | CCGGGAGGTTGGGGG[G/T]TGGGGGGGGGGCAGA | 7088 |
rs7035662 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | TLE1 | GRCh38.p7 | 9:81608092 | CACACAAGGATGACC[A/G]GGCAGCTGAGTGGAC | 7088 |
rs7036720 | snp | C/G | 0.213937 | 0.247385 | intron-variant | TLE1 | GRCh38.p7 | 9:81595749 | gcgtgaacctgggag[C/G]cggagcttgtggtga | 7088 |
rs7036755 | snp | C/T | 0.34437 | 0.231505 | intron-variant | TLE1 | GRCh38.p7 | 9:81595923 | CAAAGATCTCGGTGC[C/T]ATGAGAGAAATTACA | 7088 |
rs7037934 | snp | A/G | 0.111576 | 0.20818 | intron-variant | TLE1 | GRCh38.p7 | 9:81648713 | AGAGTCTTTCAATCA[A/G]TTATCCCTGCATTCA | 7088 |
rs7039820 | snp | G/T | 0.306044 | 0.243637 | intron-variant | TLE1 | GRCh38.p7 | 9:81600059 | TTCTAGGACCTAACT[G/T]CCTCTATCAATTACA | 7088 |
rs7040376 | snp | A/G | 0.187053 | 0.241946 | intron-variant | TLE1 | GRCh38.p7 | 9:81637091 | AACTGGGGAAGGTGG[A/G]TCATGCCTGTAATCC | 7088 |
rs7041427 | snp | A/G | 0.47802 | 0.102502 | intron-variant | TLE1 | GRCh38.p7 | 9:81624945 | ATTTTCTACACCTAC[A/G]TATGGCATACACTTG | 7088 |
rs7041471 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81597309 | GTGAAGATACGTTGA[A/G]TTGAGGGCTTTATCT | 7088 |
rs7043040 | snp | C/T | 0.302936 | 0.244331 | intron-variant | TLE1 | GRCh38.p7 | 9:81680296 | TAGTTCATGGCCACT[C/T]CCCACAGGACAGGTA | 7088 |
rs7043136 | snp | A/G | 0.303187 | 0.244277 | intron-variant | TLE1 | GRCh38.p7 | 9:81680221 | GACTTGCCCAGTCCC[A/G]AATGGAAATCCCCAA | 7088 |
rs7043209 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615543 | atctctactaaaaat[A/C]caaaaaaaaaaaaaa | 7088 |
rs7044143 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81660753 | GAAATACGGCCAAGG[A/G]CCTCAGAGATCAGCA | 7088 |
rs7044216 | snp | C/T | 0.303187 | 0.244277 | intron-variant | TLE1 | GRCh38.p7 | 9:81681746 | TGCTCAGTAGTTTTA[C/T]CTACCCATGGCCTGT | 7088 |
rs7044493 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | TLE1 | GRCh38.p7 | 9:81628957 | ATCCATGAATGCCAC[C/T]GCGTAGGTCTATACA | 7088 |
rs7045031 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | TLE1 | GRCh38.p7 | 9:81597669 | CCTACAGATCAGGAT[C/G]GCTTCTGCTTCTGAA | 7088 |
rs7045319 | snp | C/T | 0.444799 | 0.156695 | intron-variant | TLE1 | GRCh38.p7 | 9:81618867 | ACCCTTCTGCAAATA[C/T]AAACCTTCACAGGAC | 7088 |
rs7045812 | snp | C/T | 0.207559 | 0.246371 | intron-variant | TLE1 | GRCh38.p7 | 9:81598312 | TGCGCACAAACTGTT[C/T]CCTCCCGCTAGAACA | 7088 |
rs7047203 | snp | G/T | 0.427423 | 0.176128 | intron-variant | TLE1 | GRCh38.p7 | 9:81643709 | tcagctaattttttt[G/T]attttcagtggaaaa | 7088 |
rs7047448 | snp | C/T | 0.0818113 | 0.184966 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586302 | gattacaggcgtgag[C/T]ctccgtgcctggcct | 7088 |
rs7048726 | snp | C/T | 0.477937 | 0.102688 | intron-variant | TLE1 | GRCh38.p7 | 9:81622609 | TCTATGTGTTCAAAG[C/T]TACTACTGTAATTTC | 7088 |
rs7847046 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | TLE1 | GRCh38.p7 | 9:81639489 | GTTTACAGTAATTAG[A/G]AAATTTGCTTAAAAG | 7088 |
rs7849605 | snp | A/G | 0.472522 | 0.113946 | intron-variant | TLE1 | GRCh38.p7 | 9:81617518 | accagcctggccaac[A/G]tggtgaaaccctgtc | 7088 |
rs7851717 | snp | A/T | 0.463559 | 0.129972 | intron-variant | TLE1 | GRCh38.p7 | 9:81641582 | caatagtacaaaaat[A/T]aaaaaataagtatcc | 7088 |
rs7853021 | snp | G/T | 0.489665 | 0.0711382 | intron-variant | TLE1 | GRCh38.p7 | 9:81675708 | CACTAGTTTTTTTTT[G/T]TTTTTTTTTTTGAGA | 7088 |
rs7853593 | snp | A/G | 0.17461 | 0.238362 | intron-variant | TLE1 | GRCh38.p7 | 9:81646310 | CCAAAGGAGAAACGG[A/G]CTGCGAAGACTTCTT | 7088 |
rs7853703 | snp | C/T | 0.497558 | 0.0348586 | intron-variant | TLE1 | GRCh38.p7 | 9:81646307 | TAACCAAAGGAGAAA[C/T]GGACTGCGAAGACTT | 7088 |
rs7853935 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | TLE1 | GRCh38.p7 | 9:81646460 | TATTTAGTCTTCTCT[C/T]GGTAGCAGGATATGC | 7088 |
rs7854019 | snp | C/G | 0.495891 | 0.0451408 | intron-variant | TLE1 | GRCh38.p7 | 9:81646371 | AATAAAAGGGCTAGA[C/G]TGTTGGAATTTAAGT | 7088 |
rs7855913 | snp | C/T | 0.430136 | 0.173352 | intron-variant | TLE1 | GRCh38.p7 | 9:81642556 | aaaattagccaggca[C/T]ggtggtgggtgccta | 7088 |
rs7856380 | snp | C/T | 0.225597 | 0.248806 | intron-variant | TLE1 | GRCh38.p7 | 9:81622027 | AGCCGGCTGGATCCC[C/T]GAACTAATTACCTAG | 7088 |
rs7856583 | snp | A/G | 0.349452 | 0.229367 | intron-variant | TLE1 | GRCh38.p7 | 9:81629529 | AATAAGAAACTTTAA[A/G]GCAGTTTCCATAAAA | 7088 |
rs7860218 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TLE1 | GRCh38.p7 | 9:81652707 | taatcccagcacttt[A/G]ggaggccaagacagg | 7088 |
rs7860224 | snp | A/G | 0.15698 | 0.23205 | intron-variant | TLE1 | GRCh38.p7 | 9:81595233 | TATCGAGTCCACATG[A/G]TATTTCAACATGCAC | 7088 |
rs7860431 | snp | C/T | 0.424348 | 0.179172 | intron-variant | TLE1 | GRCh38.p7 | 9:81595294 | ACTTATTATGGGATA[C/T]TTGGAGTCATAATCA | 7088 |
rs7865343 | snp | A/G | 0.432357 | 0.171014 | intron-variant | TLE1 | GRCh38.p7 | 9:81613678 | CATTAACTTGTGAGC[A/G]AGAAATGTTGACCTT | 7088 |
rs7865507 | snp | C/G | 0.39979 | 0.200158 | intron-variant | TLE1 | GRCh38.p7 | 9:81613980 | TGGCGCAATCTCGGC[C/G]TACTACAAGCTCCGC | 7088 |
rs7869589 | snp | C/G | 0.43221 | 0.171171 | intron-variant | TLE1 | GRCh38.p7 | 9:81642617 | gagaactgcttgaac[C/G]caagagatagaggtt | 7088 |
rs7871288 | snp | A/T | 0.328616 | 0.237317 | intron-variant | TLE1 | GRCh38.p7 | 9:81630763 | TTTATTAAATAGATA[A/T]GTACTATAATATTTT | 7088 |
rs9886672 | snp | A/T | 0.471863 | 0.115225 | intron-variant | TLE1 | GRCh38.p7 | 9:81599904 | CACTCTATTTTCATT[A/T]ATTTTTTTTAAAGGC | 7088 |
rs10118404 | snp | A/G | 0.300926 | 0.244758 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689351 | GGTGGGGCCAGCGGG[A/G]GTTTTGGTCGCCGCG | 7088 |
rs10118624 | snp | A/G | 0.344815 | 0.231323 | intron-variant | TLE1 | GRCh38.p7 | 9:81647068 | ATAGGTTATATGTAA[A/G]CAAACTCAAATTTCT | 7088 |
rs10119840 | snp | C/T | 0.306182 | 0.243605 | intron-variant | TLE1 | GRCh38.p7 | 9:81666394 | AGAAATTAGGTAATA[C/T]CACACAATGGCAGGA | 7088 |
rs10119841 | snp | C/T | 0.306431 | 0.243548 | intron-variant | TLE1 | GRCh38.p7 | 9:81666397 | AATTAGGTAATACCA[C/T]ACAATGGCAGGATTA | 7088 |
rs10124360 | snp | A/C | 0.333491 | 0.235646 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689016 | GGGGCTACTCCACCG[A/C]GAGCAGTCCCGCAAG | 7088 |
rs10429620 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | TLE1 | GRCh38.p7 | 9:81677287 | GTAAACAACTCAggc[C/T]gggcgcagtggctca | 7088 |
rs10568227 | in-del | -/AC | 0.0599851 | 0.162463 | intron-variant | TLE1 | GRCh38.p7 | 9:81662234 | AGAGAACAGTTAAAT[-/AC]GCTACACACCAACCC | 7088 |
rs10577556 | in-del | -/CC | 0.413076 | 0.18949 | intron-variant | TLE1 | GRCh38.p7 | 9:81667718 | AGCTGTATTCCTGCT[-/CC]CCCCCAAGCTGAGTG | 7088 |
rs10627692 | in-del | -/GAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641239 | AAAAATAAAGAAGAA[-/GAA]AACTGGTATGCTACG | 7088 |
rs10682343 | in-del | -/AAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641231 | AAATAAATAAAAATA[-/AAG]AAAGAAGAAAACTGG | 7088 |
rs10694566 | in-del | -/CAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618044 | CAACAACAACAACAA[-/CAA]AAAATTCAATGATGC | 7088 |
rs10696235 | in-del | -/T/TT | 0.362523 | 0.223246 | intron-variant | TLE1 | GRCh38.p7 | 9:81665862 | CATTTTTTTTTTTTT[-/T/TT]AAAGAATTCAGTTGC | 7088 |
rs10715568 | in-del | -/A | 0.476918 | 0.104919 | intron-variant | TLE1 | GRCh38.p7 | 9:81673273 | AGCGAGACTTCATTT[-/A]AAAAAAAAAAAAAAA | 7088 |
rs10780523 | snp | A/T | 0.363359 | 0.222822 | intron-variant | TLE1 | GRCh38.p7 | 9:81632322 | ACTCCTCCACGCACA[A/T]CCAGATACATGAAAT | 7088 |
rs10780524 | snp | A/G | 0.397271 | 0.202018 | intron-variant | TLE1 | GRCh38.p7 | 9:81632538 | GCTATGTTCAGAAAG[A/G]AGGAGGCAAAACCTG | 7088 |
rs10780525 | snp | C/T | 0.309154 | 0.242901 | intron-variant | TLE1 | GRCh38.p7 | 9:81642017 | ACAAGAGCAAAACTC[C/T]ATCTCCAAAAAAAAA | 7088 |
rs10780526 | snp | A/T | 0.34526 | 0.23114 | intron-variant | TLE1 | GRCh38.p7 | 9:81647522 | CACATCCCTGTAACC[A/T]CTAAAGACAAAGGAG | 7088 |
rs10867777 | snp | C/T | 0.489318 | 0.0722982 | intron-variant | TLE1 | GRCh38.p7 | 9:81599546 | GAAAACTAATAAAGG[C/T]GGTGGCTGGGAGGAA | 7088 |
rs10867778 | snp | A/G | 0.428635 | 0.174898 | intron-variant | TLE1 | GRCh38.p7 | 9:81607315 | CATGATATTACTTCT[A/G]TCTTACAACTGACCC | 7088 |
rs10867779 | snp | C/T | 0.449345 | 0.150869 | intron-variant | TLE1 | GRCh38.p7 | 9:81610737 | GCCAAGAGGAATCCA[C/T]ACCTGCCCCCCCTCC | 7088 |
rs10867780 | snp | A/C | 0.295599 | 0.245806 | intron-variant | TLE1 | GRCh38.p7 | 9:81617537 | TGAAACCCTGTCTCT[A/C]CTAAAAATACAAAAA | 7088 |
rs10867781 | snp | C/T | 0.358728 | 0.225118 | intron-variant | TLE1 | GRCh38.p7 | 9:81618977 | TAACCATCTATCCAA[C/T]CAGACAAACCTAGTA | 7088 |
rs10867782 | snp | A/G | 0.304188 | 0.244057 | intron-variant | TLE1 | GRCh38.p7 | 9:81623231 | TTGTGATTTCTCCTC[A/G]TGCACTCCCTACTGT | 7088 |
rs10867783 | snp | C/T | 0.46974 | 0.119223 | intron-variant | TLE1 | GRCh38.p7 | 9:81623897 | AGGCCAAAGCAACCA[C/T]TGAGACATTTCGTTC | 7088 |
rs10867784 | snp | A/C | 0.17461 | 0.238362 | intron-variant | TLE1 | GRCh38.p7 | 9:81635048 | GCTCAAAGGCACTGA[A/C]TAAATTGCTGAAACT | 7088 |
rs10867785 | snp | C/G | 0.434543 | 0.168653 | intron-variant | TLE1 | GRCh38.p7 | 9:81639007 | tggctcactgcagct[C/G]aaatgcctgggctca | 7088 |
rs10867786 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | TLE1 | GRCh38.p7 | 9:81639018 | agctcaaatgcctgg[A/G]ctcaagcaatcctct | 7088 |
rs10867787 | snp | A/G | 0.202959 | 0.245534 | intron-variant | TLE1 | GRCh38.p7 | 9:81639904 | GAAAAAGCATTTTTG[A/G]TAAGCAATGACAGTT | 7088 |
rs10867788 | snp | C/T | 0.422944 | 0.180528 | intron-variant | TLE1 | GRCh38.p7 | 9:81642608 | CTGAGGCAGGAGAAC[C/T]GCTTGAACCCAAGAG | 7088 |
rs10867789 | snp | A/G | 0.308166 | 0.243139 | intron-variant | TLE1 | GRCh38.p7 | 9:81643995 | GGTTTTGATTGAAAA[A/G]ATGTTCAACATCATC | 7088 |
rs10867790 | snp | C/T | 0.421051 | 0.182323 | intron-variant | TLE1 | GRCh38.p7 | 9:81646068 | AGCAATCACAGCACA[C/T]GTTTACCTATGAAAC | 7088 |
rs10867791 | snp | C/T | 0.348794 | 0.229651 | intron-variant | TLE1 | GRCh38.p7 | 9:81647772 | TAGATGGCAGCTAAG[C/T]ATCCTCCCCAAGTCC | 7088 |
rs10867792 | snp | C/G | 0.270892 | 0.249126 | intron-variant | TLE1 | GRCh38.p7 | 9:81649511 | GGAATGAGAATGTTT[C/G]GGCTCATTTGCATTT | 7088 |
rs10867793 | snp | A/T | 0.358515 | 0.225221 | intron-variant | TLE1 | GRCh38.p7 | 9:81669827 | GTTAATAACCCTGAC[A/T]TTATACCAACGGTCC | 7088 |
rs10867794 | snp | C/T | 0.301932 | 0.244547 | intron-variant | TLE1 | GRCh38.p7 | 9:81682029 | GGTGGGTGGATCACT[C/T]GAGGTCAGGAGTTCG | 7088 |
rs10867795 | snp | A/G | 0.330016 | 0.236849 | intron-variant | TLE1 | GRCh38.p7 | 9:81682781 | CTACTGTATAGAGAT[A/G]TCTAGAGTTTACCAT | 7088 |
rs10867796 | snp | A/G | 0.300926 | 0.244758 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689140 | AGAAAGAAGACCGAG[A/G]AAGAAGGAGCTCGGA | 7088 |
rs11139331 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584965 | ATAGGCACTCATCCA[C/T]CCATCCATCCATCCA | 7088 |
rs11139332 | snp | A/G | 0.123105 | 0.215401 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586063 | TGCTCTGTCGCCCAG[A/G]CTGGAGTGAAGCGGC | 7088 |
rs11139333 | snp | C/T | 0.126909 | 0.217598 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586306 | ACAGGCGTGAGCCTC[C/T]GTGCCTGGCCTTGTT | 7088 |
rs11139334 | snp | A/C | 0.215747 | 0.247642 | intron-variant | TLE1 | GRCh38.p7 | 9:81594479 | TAAATGGGAGTTGGA[A/C]AATGAGAACAATGAG | 7088 |
rs11139336 | snp | C/T | 0.208779 | 0.246578 | intron-variant | TLE1 | GRCh38.p7 | 9:81605567 | ATATGGGCAGTCATA[C/T]GTAGAAAGCTGAAAC | 7088 |
rs11139339 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81612633 | CTGCAAGGAGCACGG[C/T]TGGGCCAGCCAAACC | 7088 |
rs11139340 | snp | C/T | 0.354665 | 0.227036 | intron-variant | TLE1 | GRCh38.p7 | 9:81614045 | CCTGAGTAGCTGGGA[C/T]TACAGGTGCCCGCCA | 7088 |
rs11139341 | snp | A/G | 0.444444 | 0.157135 | intron-variant | TLE1 | GRCh38.p7 | 9:81615119 | AAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAGAAG | 7088 |
rs11139342 | snp | C/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81619999 | AAAGCTTTTGTGACA[C/T]TATAATTTTTACTCT | 7088 |
rs11139343 | snp | A/G | 0.251859 | 0.249993 | intron-variant | TLE1 | GRCh38.p7 | 9:81620883 | ATTCTTTCCCACTGC[A/G]ACTTCCTGGTCAGGA | 7088 |
rs11139344 | snp | C/T | 0.31014 | 0.242659 | intron-variant | TLE1 | GRCh38.p7 | 9:81624122 | TCCACCCTGGCTCTT[C/T]CAACTACTGCACTTA | 7088 |
rs11139345 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | TLE1 | GRCh38.p7 | 9:81624255 | AATAGAAACGTGTAA[C/T]TTTTAAATGAACATT | 7088 |
rs11139346 | snp | C/T | 0.412583 | 0.189912 | intron-variant | TLE1 | GRCh38.p7 | 9:81626527 | ACAACATGGACAAAG[C/T]TGAAAATCTGTCCAC | 7088 |
rs11139347 | snp | A/G | 0.449853 | 0.150196 | intron-variant | TLE1 | GRCh38.p7 | 9:81627855 | ATGCTGAGAACCATC[A/G]GTAACTGCCACCTTG | 7088 |
rs11139348 | snp | A/G | 0.395818 | 0.203069 | intron-variant | TLE1 | GRCh38.p7 | 9:81629177 | TTTGTCAAATGACTC[A/G]AAGTATTTAAAAGCA | 7088 |
rs11139349 | snp | A/G | 0.301429 | 0.244653 | intron-variant | TLE1 | GRCh38.p7 | 9:81629216 | TATAAATTTTTTTAA[A/G]CCATACAACTTTTTG | 7088 |
rs11139350 | snp | C/T | 0.369142 | 0.219784 | intron-variant | TLE1 | GRCh38.p7 | 9:81633704 | CTAAGTAGTAACAGA[C/T]GCAATTATCAAACCT | 7088 |
rs11139351 | snp | C/T | 0.421368 | 0.182025 | intron-variant | TLE1 | GRCh38.p7 | 9:81637444 | GGGGCTTTGCCACAG[C/T]TGTGAAGTAAACTTT | 7088 |
rs11139352 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81639889 | accgcgcccagctGA[A/G]AAAAAGCATTTTTGA | 7088 |
rs11139353 | snp | C/G | 0.27278 | 0.24896 | intron-variant | TLE1 | GRCh38.p7 | 9:81641131 | TGTTGACAGTTCTCT[C/G]CAAATCACTCTTCCT | 7088 |
rs11139354 | snp | A/G | 0.432504 | 0.170857 | intron-variant | TLE1 | GRCh38.p7 | 9:81642810 | CTATTCACGAGAGCC[A/G]AGATACCGAACAACC | 7088 |
rs11139355 | snp | A/T | 0.427575 | 0.175975 | intron-variant | TLE1 | GRCh38.p7 | 9:81643996 | GTTTTGATtgaaaag[A/T]tgttcaacatcatca | 7088 |
rs11139356 | snp | A/G | 0.427423 | 0.176128 | intron-variant | TLE1 | GRCh38.p7 | 9:81645036 | AAAGGTGAATTTCAT[A/G]GTGTATATATCATAT | 7088 |
rs11139357 | snp | C/T | 0.113334 | 0.209338 | intron-variant | TLE1 | GRCh38.p7 | 9:81651556 | CTCTTTTCATTGGTG[C/T]GTGACTTAAAAATTC | 7088 |
rs11139358 | snp | C/T | 0.113334 | 0.209338 | intron-variant | TLE1 | GRCh38.p7 | 9:81651610 | AAGAGCCAACAGTTC[C/T]ATAGGTTCGAATACC | 7088 |
rs11139359 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | TLE1 | GRCh38.p7 | 9:81654732 | AGCCACTGCAGCTGC[A/G]GCACTGTCAAAGCAG | 7088 |
rs11139360 | snp | C/G | 0.271162 | 0.249103 | intron-variant | TLE1 | GRCh38.p7 | 9:81661977 | CTGGGCAATGTGTTT[C/G]AAGAGCATGAAATTA | 7088 |
rs11139362 | snp | A/G | 0.396182 | 0.202807 | intron-variant | TLE1 | GRCh38.p7 | 9:81666700 | GAATCGCTTGAACCC[A/G]GGAAGCGGAGGTTGC | 7088 |
rs11139363 | snp | A/C | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81668548 | TCACTGCATCATTAT[A/C]CAATCCACAGAGGAA | 7088 |
rs11139364 | snp | C/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81679699 | CCACTATACTAAATA[C/T]CCTGTAGTAAAGGTA | 7088 |
rs11139365 | snp | A/C | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81681747 | GCTCAGTAGTTTTAT[A/C]TACCCATGGCCTGTG | 7088 |
rs11139366 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81683602 | GGATGTTTTTCAAAT[A/G]TAAGTCCACTTTAAA | 7088 |
rs11139367 | snp | A/G | 0.340108 | 0.233197 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686738 | GTCTCATTACTTGAA[A/G]AAACTAAGGCTGAGA | 7088 |
rs11301991 | in-del | -/A | 0.488726 | 0.0742286 | intron-variant | TLE1 | GRCh38.p7 | 9:81595833 | AAAAAAAAAAAAAAA[-/A]TTAAAAAATAAAAGT | 7088 |
rs11322598 | in-del | -/A | 0.371785 | 0.218331 | intron-variant | TLE1 | GRCh38.p7 | 9:81680883 | TGTTGACTTAGGGGG[-/A]AAAAAAATCTCAAAG | 7088 |
rs11375860 | in-del | -/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81637662 | TTTTTTTTTTTTTTT[-/T]AAGCAAAATCCTATC | 7088 |
rs11376391 | in-del | -/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81632496 | TTTTTTTTTTTTTTT[-/T]TTACCATATTAAACA | 7088 |
rs11436586 | in-del | -/T | 0.109814 | 0.206997 | intron-variant | TLE1 | GRCh38.p7 | 9:81622441 | CTTCTTAATGTCTTG[-/T]TTTTTTTTTGTTGTT | 7088 |
rs11788359 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615239 | gaggctgaggcagga[A/G]aattgtttgaacctg | 7088 |
rs11788381 | snp | A/G | 0.277778 | 0.248452 | intron-variant | TLE1 | GRCh38.p7 | 9:81615330 | tgagactccgtctca[A/G]aaaaaaaaaaaaaga | 7088 |
rs11788383 | snp | A/G | 0.0144571 | 0.0837826 | intron-variant | TLE1 | GRCh38.p7 | 9:81615352 | aaaaaaagaaTCTCA[A/G]AAGTTTGAACCATTT | 7088 |
rs11788532 | snp | C/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691093 | TCCATAAGGGCACAT[C/T]TTGGACAAGTATTTA | 7088 |
rs11791162 | snp | A/G | 0.0883596 | 0.190715 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583300 | AAAGGGAAAAGGAAG[A/G]GGAGATTGGGCCTTC | 7088 |
rs11792087 | snp | C/T | 0.268995 | 0.249277 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587969 | CAGTGTCTGCTGATG[C/T]GCAAGATCAAACTAA | 7088 |
rs11794460 | snp | C/T | 0.322007 | 0.239405 | intron-variant | TLE1 | GRCh38.p7 | 9:81643092 | gaaaatgaggagcaa[C/T]tggtcaaagggtaca | 7088 |
rs11999172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81637028 | aaaagaaaaaagaaa[A/G]aaaaAGATTTCCCCT | 7088 |
rs11999426 | snp | C/T | 0.425277 | 0.178263 | intron-variant | TLE1 | GRCh38.p7 | 9:81646209 | AACTACAAAGCATGA[C/T]GACAATAATCCGGAC | 7088 |
rs12002982 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | TLE1 | GRCh38.p7 | 9:81672506 | TTAGTACATCAGCAG[A/C]AGCTGTGAACCTTGA | 7088 |
rs12003063 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | TLE1 | GRCh38.p7 | 9:81666901 | ggtaagaggatcacc[A/G]cagagcaggagttca | 7088 |
rs12004638 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81645179 | agcctgaccaacatg[C/G]agaaaccctgtctct | 7088 |
rs12005124 | snp | A/G | 0.395635 | 0.2032 | intron-variant | TLE1 | GRCh38.p7 | 9:81645598 | atacaaaattagcca[A/G]gcgtggtggcacatg | 7088 |
rs12005217 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637178 | gcctgaccaacatag[G/T]gaaaccctgtctcta | 7088 |
rs12006077 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81643817 | ctgggattacatgtg[G/T]gagccaccatgcctg | 7088 |
rs12057062 | snp | A/G | 0.312348 | 0.242101 | intron-variant | TLE1 | GRCh38.p7 | 9:81628342 | AGCCAGAATTCCACT[A/G]AAGTCTGCCTTTGTA | 7088 |
rs12235177 | snp | C/T | 0.428333 | 0.175206 | intron-variant | TLE1 | GRCh38.p7 | 9:81645455 | aacacaaaagataaa[C/T]gcttgctgggtctgg | 7088 |
rs12235264 | snp | C/T | 0.499954 | 0.00479211 | intron-variant | TLE1 | GRCh38.p7 | 9:81609067 | GCCCCCTCCCCTCCC[C/T]TTTCCTCTCCTCTCC | 7088 |
rs12236029 | snp | A/T | 0.444444 | 0.157135 | intron-variant | TLE1 | GRCh38.p7 | 9:81623617 | AACCCCATCTGTACT[A/T]AAAAAAAAAAAAAAA | 7088 |
rs12237158 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609178 | caacctccgccaccc[A/G]ggttcaagcgattct | 7088 |
rs12337840 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691388 | GAAAAAATAAAAAAG[C/T]GATTTTAACCAGTCT | 7088 |
rs12339574 | snp | A/G | 0.19334 | 0.243495 | intron-variant | TLE1 | GRCh38.p7 | 9:81592186 | acatggtgaaacccc[A/G]tctctactaaaaata | 7088 |
rs12343077 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | TLE1 | GRCh38.p7 | 9:81635295 | CTAGAATGGGTAGGA[C/T]CGTGGATGAGGAAAG | 7088 |
rs12346038 | snp | A/T | 0.0592355 | 0.161582 | intron-variant | TLE1 | GRCh38.p7 | 9:81655243 | atggtgggcgcctgt[A/T]ataccagctactcgg | 7088 |
rs12346622 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81673403 | GGGAAAATCAGTTCA[A/G]AGGTAGGAAGGAAGC | 7088 |
rs12346652 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81673464 | GTGAAGCATGGCCTA[A/G]AAGTCCAAGAGCAGG | 7088 |
rs12346664 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81673526 | CACAGCTATCCCTCA[A/G]AGCGCCCCCAtgcca | 7088 |
rs12347874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674498 | CCAAGGTCCCTGAGG[C/T]CAACTGAAAATCTCC | 7088 |
rs12378468 | snp | A/G | 0.192715 | 0.243348 | intron-variant | TLE1 | GRCh38.p7 | 9:81636633 | AAAATCTAGAATGGA[A/G]TCACCAGAAGATGAC | 7088 |
rs12379295 | snp | C/T | 0.341235 | 0.232758 | intron-variant | TLE1 | GRCh38.p7 | 9:81630089 | TCAGTCTCTGATTTC[C/T]GCACTTGGTATAAAT | 7088 |
rs12379312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81660279 | CCATGCACCCCTAAA[C/T]TCAATGGCCAAGGTG | 7088 |
rs12551040 | snp | A/G | 0.432651 | 0.170701 | intron-variant | TLE1 | GRCh38.p7 | 9:81642069 | cctcaaacctgctga[A/G]atggtgggtaacaaa | 7088 |
rs12555026 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | TLE1 | GRCh38.p7 | 9:81676129 | TGTGTGTAAAAACAT[A/G]TACAAACTTTTCTTG | 7088 |
rs12555310 | snp | G/T | 0.0988009 | 0.199095 | intron-variant | TLE1 | GRCh38.p7 | 9:81643245 | ttttttgttttttgg[G/T]ttttttttttgacag | 7088 |
rs12684630 | snp | A/C | 0.00938946 | 0.0678717 | intron-variant | TLE1 | GRCh38.p7 | 9:81600910 | tctacctgctgctct[A/C]gattatcagtgctac | 7088 |
rs12686261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621820 | TCAAAACTGAGGACC[A/G]GAAGGCAATCCCAAG | 7088 |
rs12686341 | snp | A/T | 0.266 | 0.249487 | intron-variant | TLE1 | GRCh38.p7 | 9:81619389 | GAGCAGAGATACTAC[A/T]GCTGGCTCCAGCAAA | 7088 |
rs13283691 | snp | C/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81675524 | GTTTTGTTTATCTCT[C/T]TTTTTTAGTCCAAAC | 7088 |
rs13285167 | snp | C/T | 0.187369 | 0.242028 | intron-variant | TLE1 | GRCh38.p7 | 9:81604764 | CTCAGGAGGCACTCA[C/T]CCACCTGCACATGGA | 7088 |
rs13285672 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599924 | TTTTTAAAGGCAAAT[A/G]CAAAACTTCTTAAAA | 7088 |
rs13286197 | snp | A/G | 0.0803491 | 0.183626 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687792 | TGACCCCGGGGACCA[A/G]AGGAGAAAAACAACT | 7088 |
rs13287073 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599923 | TTTTTTAAAGGCAAA[G/T]ACAAAACTTCTTAAA | 7088 |
rs13289712 | snp | A/T | 0.208474 | 0.246527 | intron-variant | TLE1 | GRCh38.p7 | 9:81597546 | CAAACTGCAGGGCAG[A/T]CAGTCAGTCCTGGAT | 7088 |
rs13291018 | snp | A/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81615141 | aagaagaagaaGGCA[A/T]TGAACATGGATGCGT | 7088 |
rs13299053 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81683377 | GTTTCCCCCTAGAGA[A/G]AATTCCTGTCAAATC | 7088 |
rs13299677 | snp | G/T | 0.228253 | 0.249052 | intron-variant | TLE1 | GRCh38.p7 | 9:81632034 | GGCGGAGGTTGCAGT[G/T]AGCCGAGATAGTGCT | 7088 |
rs13299835 | snp | G/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81683340 | AATAATTTCAGCCTG[G/T]CAGGAGTCTCGCTAA | 7088 |
rs17080511 | snp | C/T | 0.000356374 | 0.0133439 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687452 | CGTCCCTCGGTCCCC[C/T]TCGCTGGTCGCCCCC | 7088 |
rs17084991 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TLE1 | GRCh38.p7 | 9:81656251 | GTCATGGCTCTCCTC[A/G]AAAGCATGGGCAAGG | 7088 |
rs17085015 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687950 | GTTTCTCTCCTGCAG[C/T]CATATCCCCTCTACC | 7088 |
rs17294206 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588041 | TTTCCCTGTTTTCCA[C/T]GATCCAAGTGCTAAA | 7088 |
rs17295330 | snp | A/C | 0.0955749 | 0.196603 | intron-variant | TLE1 | GRCh38.p7 | 9:81670237 | TAACCAGTATGCGAC[A/C]AACAGTAGAATCTGG | 7088 |
rs17851325 | snp | A/G | | | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634170 | CCCACTCAGAGCACT[A/G]GACAGCGCAAGAAGG | 7088 |
rs28481611 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | TLE1 | GRCh38.p7 | 9:81640465 | CTGGGAAATTTTACA[C/T]ACTGGTGTTCTGGGG | 7088 |
rs28515767 | snp | A/T | 0.0737376 | 0.17729 | intron-variant | TLE1 | GRCh38.p7 | 9:81640877 | ATGCCCACCTTCTCC[A/T]GACCGGAAACTAAGC | 7088 |
rs33934053 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663623 | CGCACAGAATAGACT[-/T]TTTTTTTTTTTTTTT | 7088 |
rs33949142 | in-del | -/AAC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618028 | AGACTCCGTCTCAAA[-/AAC]ACAACAACAACAACA | 7088 |
rs34015917 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653941 | AGAGAAGCAACATAA[-/T]TTGCACTTTAACAGC | 7088 |
rs34102071 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647214 | CCCCACTGGTCATCT[-/G]GACGATGTCTTCTAA | 7088 |
rs34151164 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671771 | AGGGTAGTCGATTAT[-/A]AAAATACAGATTTCT | 7088 |
rs34179903 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661223 | ATATATATATATATC[-/T]TTTTTTCAAGATATG | 7088 |
rs34263355 | in-del | -/T/TT | 0.476574 | 0.105661 | intron-variant | TLE1 | GRCh38.p7 | 9:81672463 | ATTTTTTTTTTTTTT[-/T/TT]GCTTCCCCAAATATT | 7088 |
rs34294805 | in-del | -/TG | 0.109461 | 0.206758 | intron-variant | TLE1 | GRCh38.p7 | 9:81656257 | CTCTCCTCGAAAGCA[-/TG]TGGGCAAGGCTTTCC | 7088 |
rs34328471 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607060 | AGACCCAGTGTCTCT[-/A]AAAAAAAAAAAAAAA | 7088 |
rs34401117 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687122 | ACAGTGCAAACCGGC[-/A]AAAGGGAAACAATGG | 7088 |
rs34409193 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648651 | CAGGTAGAAGAGAGC[-/T]TTTAGTTCCAAACTC | 7088 |
rs34467900 | snp | A/G | 0.162581 | 0.234218 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687095 | TAAAGACATGAAAAA[A/G]GACTCCCTGGAACAG | 7088 |
rs34522700 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615421 | TATCCCCCAAGTAAG[-/C]ACGGCAATGAGGCTG | 7088 |
rs34526060 | in-del | -/A | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81645373 | CCAAAAAAAAAAAAA[-/A]TAATAGTAATAATAA | 7088 |
rs34564844 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TLE1 | GRCh38.p7 | 9:81660017 | CAGCACTTACTGTCA[C/T]TTGGTAAACTAAACC | 7088 |
rs34569728 | in-del | -/AAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641232 | AATAAATAAAAATAA[-/AAG]AGAAGAAAACTGGTA | 7088 |
rs34601196 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638717 | CAATCTCCTCCTTCT[-/G]GGGTTCAAGCGATTC | 7088 |
rs34606017 | in-del | -/C | | | frameshift-variant | TLE1 | GRCh38.p7 | 9:81585550 | GCTCTCATGCAGGTG[-/C]CAGCTGGTACTTGTC | 7088 |
rs34610877 | in-del | -/AT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661220 | TTTATATATATATAT[-/AT]CTTTTTTTCAAGATA | 7088 |
rs34624152 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628929 | GCAAAAGAGCACGGA[-/C]CCCACCCAGTCCATC | 7088 |
rs34624864 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657905 | TCACTACAGACATAA[-/T]TTTTTTTTTTTTTTT | 7088 |
rs34716608 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673272 | AGCGAGACTTCATTT[-/A]AAAAAAAAAAAAAAA | 7088 |
rs34739928 | snp | A/G | 0.333952 | 0.235483 | intron-variant | TLE1 | GRCh38.p7 | 9:81673701 | CCGCCCCCTCCCCGT[A/G]TCAACCTTCCCAGCC | 7088 |
rs34743384 | in-del | -/TA | 0.167809 | 0.236103 | intron-variant | TLE1 | GRCh38.p7 | 9:81661207 | ATATATATGTATTTT[-/TA]TATATATATATATCT | 7088 |
rs34823553 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606831 | TAAGATTGTATATAA[-/C]CCCAGATCCTGGCAA | 7088 |
rs34891171 | in-del | -/T | 0.416382 | 0.186593 | intron-variant | TLE1 | GRCh38.p7 | 9:81651973 | ATTAATAGATTTTTT[-/T]GTCCCCTCCTAAAAT | 7088 |
rs34947337 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615118 | TGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 7088 |
rs34964149 | snp | C/T | 0.15698 | 0.23205 | intron-variant | TLE1 | GRCh38.p7 | 9:81654319 | TATGATCATTTAATA[C/T]GGTGACTATATATAT | 7088 |
rs35036421 | in-del | -/T | | | splice-acceptor-variant, intron-variant | TLE1 | GRCh38.p7 | 9:81611959 | TCCTCAAGCCAGCTG[-/T]CTGAAAGGAAACACA | 7088 |
rs35060460 | in-del | -/T/TT/TTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675698 | AAGGACTCACACTAG[-/T/TT/TTT]TTTTTTTTTGTTTTT | 7088 |
rs35086426 | in-del | -/A | 0.428635 | 0.174898 | intron-variant | TLE1 | GRCh38.p7 | 9:81648841 | TGTTGCTTATGGTGT[-/A]AAAAACGATCCTGAT | 7088 |
rs35107385 | in-del | -/A | 0.396364 | 0.202676 | intron-variant | TLE1 | GRCh38.p7 | 9:81600629 | AGCATTTAATAGACC[-/A]AAAAAAAAAAAAAAA | 7088 |
rs35160068 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603396 | GGTTATATTGAGCTG[-/A]AAACACTTGAGAAAT | 7088 |
rs35168314 | in-del | -/A | 0.269267 | 0.249256 | intron-variant | TLE1 | GRCh38.p7 | 9:81594544 | GCAAGACTACGTCTT[-/A]AAAAAAAAAAAAATT | 7088 |
rs35206989 | in-del | -/T | 0.330947 | 0.236533 | intron-variant | TLE1 | GRCh38.p7 | 9:81678380 | CAATTAATTTTTTTT[-/T]AAATCTTTTATTGTA | 7088 |
rs35285352 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675017 | CAAAAAATAAATTTT[-/A]AAAAAAGTACATGGA | 7088 |
rs35328693 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622703 | TAAATGTGGTGGACA[-/G]GGGCTAGTAATTAGC | 7088 |
rs35355418 | in-del | -/A | 0.48498 | 0.0853497 | intron-variant | TLE1 | GRCh38.p7 | 9:81642531 | ACCCCGTCTCTACTT[-/A]AAAAAAAAAAAAATT | 7088 |
rs35440521 | in-del | -/A | 0.179552 | 0.239869 | intron-variant | TLE1 | GRCh38.p7 | 9:81594352 | ATACTATGCAGCCAT[-/A]AAAAAAAGGATGAGT | 7088 |
rs35453807 | in-del | -/AT/TA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632135 | GGAATGGCAAAACAA[-/AT/TA]TAAGGCTTCCTCCAT | 7088 |
rs35467275 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625933 | ACCTCAGAAACTACT[-/A]AAAAAAAAAAAAAAA | 7088 |
rs35473150 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661206 | TATATATATGTATTT[A/T]TATATATATATATCT | 7088 |
rs35481697 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654630 | CAGGCGTGAGCCACT[-/G]GCACCCAGCCAAGTG | 7088 |
rs35532445 | in-del | -/T | 0.46137 | 0.133501 | intron-variant | TLE1 | GRCh38.p7 | 9:81642096 | AAAAAGACAAAGATA[-/T]GTGTTAGTGATGGTG | 7088 |
rs35540125 | in-del | -/AA/AG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598727 | GGTAGCAGTTTCCTA[-/AA/AG]AGGGGGAAAGGCAGT | 7088 |
rs35556985 | in-del | -/C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637644 | TACAATGAAAGTTTC[-/C/T]TTTTTTTTTTTTTTT | 7088 |
rs35562910 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663622 | CCGCACAGAATAGAC[-/T]TTTTTTTTTTTTTTT | 7088 |
rs35568651 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638083 | ACTGCTCAGCTAACC[-/A]AGATGCTCTTGAGAA | 7088 |
rs35625309 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638084 | ACTGCTCAGCTAACC[-/A]GATGCTCTTGAGAAC | 7088 |
rs35645180 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674320 | CACTGTACTTATAAG[-/C]AAGCTCTGACCAGCT | 7088 |
rs35706245 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650059 | CTCGCTTGCATTGCG[-/C]CCTGATTCACCACTT | 7088 |
rs35737418 | in-del | -/G | | | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583806 | GGAAACAAGTTCATT[-/G]GGAGACACCACTGCT | 7088 |
rs35798665 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618772 | ACATAAGGAACTAGC[-/A]AAAAGTAGCAAACTA | 7088 |
rs35806718 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674994 | ACCTCATCTCTACTG[-/A]AAAAAATCAAAAAAT | 7088 |
rs35808742 | in-del | -/AAAAA | 0.234692 | 0.249531 | intron-variant | TLE1 | GRCh38.p7 | 9:81681552 | GAGATTCCGTCGCGC[-/AAAAA]AAAAAAAGAAAAAAA | 7088 |
rs35867645 | in-del | -/A | 0.236724 | 0.249647 | intron-variant | TLE1 | GRCh38.p7 | 9:81668169 | CAAGACTGCATCTCG[-/A]AAAAAAAAAAAAGAA | 7088 |
rs35884737 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628447 | TCTTTTTTTTTCCAG[-/A]AAAAGACCAACAGTA | 7088 |
rs35959525 | in-del | -/ACTA | 0.243919 | 0.249926 | intron-variant | TLE1 | GRCh38.p7 | 9:81628743 | ATGGTCGCTCAGATT[-/ACTA]ACTCTCAATCTGTTA | 7088 |
rs35970494 | in-del | -/C | 0.221439 | 0.248363 | intron-variant | TLE1 | GRCh38.p7 | 9:81677236 | AACGAGACTCGTCTT[-/C]CCCCCCCCCAAAAAA | 7088 |
rs36054117 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613198 | CTGAACAGAGTGCAG[C/G]TGCTGAAACCCCAGG | 7088 |
rs36086401 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661203 | TTATATATATATGTA[-/T]TTTTTATATATATAT | 7088 |
rs36108203 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660342 | ACAAAAAAAAAAAAA[-/A]CAAAATCATACGTTG | 7088 |
rs41296045 | snp | A/G | 0.000111025 | 0.00744984 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634263 | GGGAACTGGGGGTCC[A/G]TGGCCATGAGAAAGA | 7088 |
rs41308896 | snp | A/G | 0.0751996 | 0.178731 | intron-variant | TLE1 | GRCh38.p7 | 9:81634087 | TAATCTGGCTTGCCC[A/G]GCCTCTCACCTCTGT | 7088 |
rs41316498 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81633989 | GTTCCTCTTATCTCA[C/T]TGTTTGCTCTCTGTA | 7088 |
rs55688019 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | TLE1 | GRCh38.p7 | 9:81675460 | TCCAGGGACAGTAAT[A/G]CCTGCACATGCTCAA | 7088 |
rs55697345 | snp | A/C/T | 4.65149e-05 | 0.00482237 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688274 | GGCTCTGTTCCCCGG[A/C/T]AACTCAATTCTCCGG | 7088 |
rs55712377 | snp | G/T | 0.262985 | 0.249663 | intron-variant | TLE1 | GRCh38.p7 | 9:81620340 | TCTTTACAGTATTAT[G/T]TTTAAGGACATGGAA | 7088 |
rs55791956 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | TLE1 | GRCh38.p7 | 9:81596949 | GTTTAGATTCATTTA[C/G]TTATTCAAGAGGAAG | 7088 |
rs55862411 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688804 | CGCAAGATTCGGCTG[C/T]GCCTTCGGCCGGGTG | 7088 |
rs55986163 | snp | A/G | 0.31357 | 0.241783 | intron-variant | TLE1 | GRCh38.p7 | 9:81660607 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 7088 |
rs55990374 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | TLE1 | GRCh38.p7 | 9:81661116 | TGGCAGAGTGAGACT[C/T]GGTCTCAAAAATAAA | 7088 |
rs56000014 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689305 | CTCCCCGGCGGGCAA[A/G]CTCTGCG | 7088 |
rs56022025 | in-del | -/T | 0.420096 | 0.183214 | intron-variant | TLE1 | GRCh38.p7 | 9:81679305 | AAAATTTTTCTTCAC[-/T]TTTTTTTCTTTTTTT | 7088 |
rs56028327 | snp | G/T | 0.11109 | 0.207856 | intron-variant | TLE1 | GRCh38.p7 | 9:81585684 | GACAGGCTCACTCAT[G/T]ATTCCGCCTGATACA | 7088 |
rs56030321 | snp | A/G | | | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583241 | AAAAAAAAAAAAAAA[A/G]GAGAGAGAGAGAGAG | 7088 |
rs56035615 | in-del | -/A | 0.42357 | 0.179927 | intron-variant | TLE1 | GRCh38.p7 | 9:81640397 | ACAATTTCAAAAATT[-/A]AAAAAAAAAAAAAAT | 7088 |
rs56129461 | snp | A/C | 0.118933 | 0.212888 | intron-variant | TLE1 | GRCh38.p7 | 9:81604223 | TTCCCTGCACCCCAT[A/C]CTAGGCTGTGAGCTC | 7088 |
rs56255759 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627319 | CACTTTTTTTTTTTT[-/T]AAGAGTAAAGATGCC | 7088 |
rs56321152 | snp | A/C | 0.0850919 | 0.187897 | intron-variant | TLE1 | GRCh38.p7 | 9:81585217 | ATAAATTCCCGCCCA[A/C]CCCTCTTCAGAGTAG | 7088 |
rs56327119 | in-del | -/TGTGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633325 | GTGTGTGTGTGTGTG[-/TGTGTG]CAGCAGGCGTTTGAG | 7088 |
rs56692367 | in-del | -/AAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617148 | CAAAAAAAAAAAAAA[-/AAAA]GAATCCTGGAAAGCT | 7088 |
rs56842573 | in-del | -/A/AAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648285 | CAAAAAAAAAAAAAA[-/A/AAAA]CCCAAGCATCTTTAG | 7088 |
rs57065882 | snp | A/G | 0.089084 | 0.191327 | intron-variant | TLE1 | GRCh38.p7 | 9:81614816 | GAGCTCCATAATATC[A/G]GGGCATGCTCTATGA | 7088 |
rs57208048 | snp | C/G | 0.395087 | 0.203592 | intron-variant | TLE1 | GRCh38.p7 | 9:81666317 | CCTCTCCCTGGGCCA[C/G]ACCCCAAGCAAGCCT | 7088 |
rs57213987 | in-del | -/AACT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628746 | GTCGCTCAGATTACT[-/AACT]CTCAATCTGTTAACT | 7088 |
rs57243941 | snp | A/G | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686241 | CAAAATCCGGCCCTT[A/G]CACAATCTTCACTCT | 7088 |
rs57375451 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81669045 | AACCCACGTATTCTG[C/T]TACACTGGTCTGCAT | 7088 |
rs57432666 | snp | A/G | 0.351853 | 0.228311 | intron-variant | TLE1 | GRCh38.p7 | 9:81622554 | CAATAACCTTTCCGT[A/G]GCTGGACCTTTAAGA | 7088 |
rs57678617 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | TLE1 | GRCh38.p7 | 9:81641587 | GTACAAAAATTAAAA[A/C]ATAAGTATCCTAATT | 7088 |
rs57688516 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | TLE1 | GRCh38.p7 | 9:81682780 | TCTACTGTATAGAGA[C/T]ATCTAGAGTTTACCA | 7088 |
rs57789357 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | TLE1 | GRCh38.p7 | 9:81658918 | TTTATCTATTTATTT[A/T]TTTTTTTTTTAGATG | 7088 |
rs57800121 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670739 | ATTAAAAAAAAAAAA[-/A]TCACAGCTTTTTTTG | 7088 |
rs57827746 | in-del | -/GAAAGAAAG | 0.400844 | 0.212688 | intron-variant | TLE1 | GRCh38.p7 | 9:81642709 | AAAAATGAAAGAAAA[-/GAAAGAAAG]GAAAGAAAGGAAAGA | 7088 |
rs57996607 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595832 | AAAAAAAAAAAAAAA[-/AA]TTAAAAAATAAAAGT | 7088 |
rs58039255 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | TLE1 | GRCh38.p7 | 9:81654778 | TGAGGCCTAAGGTGA[C/T]AGAGTAGAAGAAAGG | 7088 |
rs58069135 | in-del | -/TTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683238 | TTTTTTTTTTTTTTT[-/TTT]AGTAACAAAGATGTT | 7088 |
rs58094348 | snp | C/T | 0.105569 | 0.204058 | intron-variant | TLE1 | GRCh38.p7 | 9:81667071 | TTGGAGTTTGGAGTT[C/T]TGATTAAGCCACTGC | 7088 |
rs58263360 | snp | A/G | 0.081446 | 0.184634 | intron-variant | TLE1 | GRCh38.p7 | 9:81614923 | TTTGAGGCCAGGTGC[A/G]GTGGCTCACACCTGT | 7088 |
rs58357123 | in-del | -/TAAA/TAAATAAA | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81666811 | AAATAAATAAATAAA[-/TAAA/TAAATAAA]ATAAAATATGCCTGT | 7088 |
rs58444047 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684148 | CCCTTCAGAGTAAAT[A/T]AAAAAAAAAAAAAAA | 7088 |
rs58773970 | in-del | -/TTAGA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663352 | GATCATAGAGCAAGA[-/TTAGA]AGCCACATATTCCCT | 7088 |
rs58907018 | in-del | -/CATC/CATCCATC/CATCCATCCATC | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81585002 | ATCCATCCATCCATC[-/CATC/CATCCATC/CATCCATCCATC]TATGCATACTGTGAA | 7088 |
rs59090455 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588406 | GTGTTAGAAAGAGCC[C/T]TGCATTAGGAAATCT | 7088 |
rs59205631 | in-del | -/A/AAA | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81607075 | AAAAAAAAAAAAAAA[-/A/AAA]TGGAGAGAGAGAGAG | 7088 |
rs59382919 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662944 | CCTCTGCTTCCTGGG[C/T]TTAAGCGATTCTCAT | 7088 |
rs59394276 | in-del | -/A/AT | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81670725 | TCAGAAAAAAAAAAA[-/A/AT]TTAAAAAAAAAAAAT | 7088 |
rs59467259 | in-del | -/A | 0.126909 | 0.217598 | intron-variant | TLE1 | GRCh38.p7 | 9:81597281 | GCACCACCACGACTT[-/A]AAAAAAAGCCAAGTG | 7088 |
rs59507110 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | TLE1 | GRCh38.p7 | 9:81652390 | CAATGCAGGCTGAAG[G/T]AGAAGGGTTTAAATG | 7088 |
rs59604053 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668713 | GTATGCCAAAAAAAA[-/A]GGCCTTCATCCCTTT | 7088 |
rs59769834 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622696 | AGTTCCTCTAAATGT[A/G]GTGGACAGGGCTAGT | 7088 |
rs59790457 | snp | C/T | 0.304438 | 0.244001 | intron-variant | TLE1 | GRCh38.p7 | 9:81620813 | GAAATGTGCTTCTGT[C/T]CTATTTACTGTTTGA | 7088 |
rs59830030 | snp | C/T | 0.081446 | 0.184634 | intron-variant | TLE1 | GRCh38.p7 | 9:81615056 | CACTGCACTCCAGCC[C/T]GGGTGACAGAGTGAG | 7088 |
rs59954581 | snp | C/T | 0.040671 | 0.13668 | intron-variant | TLE1 | GRCh38.p7 | 9:81682754 | CAATTTTCCATGAGA[C/T]ATTGTCTACCTCTAC | 7088 |
rs59999145 | snp | A/C | 0.117886 | 0.21224 | intron-variant | TLE1 | GRCh38.p7 | 9:81606575 | AGGTGGGAGCTGAAC[A/C]ATGAGAACACTTGGA | 7088 |
rs60057436 | snp | C/T | 0.139564 | 0.224285 | intron-variant | TLE1 | GRCh38.p7 | 9:81605700 | ATACCATTCAGGACA[C/T]AGGCATGGGCAAAGA | 7088 |
rs60087115 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81632300 | CCCTTTCCTTCAACC[A/G]TTCCTCACTCCTCCA | 7088 |
rs60087604 | in-del | -/ACAC/ACACACACACACAC/ACACACACACACAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652138 | CACACACACACACAC[lengthTooLong]GTAAAGCCATCAAAT | 7088 |
rs60091510 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677584 | AAAAAAAAAAAAAAA[-/A]GTAAACAACTCAGGT | 7088 |
rs60095023 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664710 | TAAGAAAAAAAAAAA[-/A]TAAGTGAGGTACCTT | 7088 |
rs60109467 | in-del | -/CATCCC/CATCCCGC/CATCCCGCCTGTGG/CATCCCGCCTGTGTGTGTGTGTGTGTGTGTGT | 0 | 0 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587927 | TGTGTGTGTGTGTGT[lengthTooLong]GTGTGTGTGTGTGTG | 7088 |
rs60144586 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TLE1 | GRCh38.p7 | 9:81639614 | TTTTGAGACAGTCTC[A/G]CTCTGTCGCCCAGGC | 7088 |
rs60188111 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | TLE1 | GRCh38.p7 | 9:81662973 | ATGCCTCAGCCTCCC[A/G]AGTGGCTGGGACTAC | 7088 |
rs60259878 | snp | C/T | 0.16911 | 0.236552 | intron-variant | TLE1 | GRCh38.p7 | 9:81595135 | ATACACATATAAAAA[C/T]AATATAGCTCAAAGC | 7088 |
rs60384577 | in-del | -/A | | | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583243 | AAAAAAAAAAAAAGG[-/A]GAGAGAGAGAGAGAA | 7088 |
rs60410635 | snp | G/T | 0.488424 | 0.0751925 | intron-variant | TLE1 | GRCh38.p7 | 9:81606800 | AACCATATATATATA[G/T]ATAGAGAGAGAGGCA | 7088 |
rs60422400 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | TLE1 | GRCh38.p7 | 9:81613133 | TGGGGGGACAAGAGC[A/G]AGACTTCGTCTCAAG | 7088 |
rs60495961 | snp | C/T | 0.192401 | 0.243274 | intron-variant | TLE1 | GRCh38.p7 | 9:81671124 | GGTGAACTGAGATCA[C/T]GCCACTGCACTGCAG | 7088 |
rs60568353 | snp | A/C | 0.0581099 | 0.160244 | intron-variant | TLE1 | GRCh38.p7 | 9:81673448 | CAAAACGGAAGTATC[A/C]GTGAAGCATGGCCTA | 7088 |
rs60617965 | in-del | -/A | 0.349671 | 0.229272 | intron-variant | TLE1 | GRCh38.p7 | 9:81684254 | CCATTTACTATCAAG[-/A]AAGTTACAAGTGCCT | 7088 |
rs60666250 | in-del | -/T | 0.423726 | 0.179776 | intron-variant | TLE1 | GRCh38.p7 | 9:81643245 | TTTTTTGTTTTTTGG[-/T]TTTTTTTTTTGACAG | 7088 |
rs60735628 | in-del | -/T/TT | 0 | 0 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586035 | TTTTTTTTTTTTTTT[-/T/TT]GAGACGGAGTCTTGC | 7088 |
rs60743951 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | TLE1 | GRCh38.p7 | 9:81601232 | AAAGTGGGGTGAAAG[A/G]GGGAAGCCCCCGGCC | 7088 |
rs60746596 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605815 | GCAAAAAAAAAAAAA[-/A]CTACCATTAGAGTGA | 7088 |
rs61098808 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674093 | CTCTAAATCAATTTT[C/T]TCCCCAGCCATCAAC | 7088 |
rs61311042 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | TLE1 | GRCh38.p7 | 9:81662432 | AGGAGCTGTGGCTCA[C/T]GCCTGTAATCCCAAC | 7088 |
rs61458315 | in-del | -/TTTTTTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675719 | TTTGTTTTTTTTTTT[-/TTTTTTTT]GAGACGGAGTCTCGC | 7088 |
rs61475842 | in-del | -/TGTGTGTGTGTG | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81633314 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTG]CAGCAGGCGTTTGAG | 7088 |
rs61504059 | in-del | -/CA | 0.462472 | 0.13174 | intron-variant | TLE1 | GRCh38.p7 | 9:81625593 | ACACAATTATGAAAC[-/CA]CATACCTTCATGTAA | 7088 |
rs61733322 | snp | C/T | 0.000345927 | 0.013147 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616057 | ACTGCTAGAAGCATC[C/T]TTCTTTAGCAGGCGA | 7088 |
rs61733323 | snp | C/G/T | 6.59859e-05 | 0.00574357 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81613389 | TACCCGCTTGGTTAA[C/G/T]GAGGGGGTCTATGGC | 7088 |
rs61733324 | snp | A/G | 0.00709094 | 0.0591201 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593124 | CACGTGTCTCGTGGG[A/G]TTGCTGATGGTCACA | 7088 |
rs61733325 | snp | A/T | 0.0867769 | 0.189363 | missense, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587689 | CAGTCACCTGGGAGG[A/T]GAAGTCGTGCTGCTG | 7088 |
rs61734164 | snp | A/G | 0.00385139 | 0.0437134 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81620540 | TCTTAGACTGTCTGG[A/G]ACCAGGAGGGAATTA | 7088 |
rs61738504 | snp | C/T | 0.00712522 | 0.0592608 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634206 | ACTGCCCCCGAGGGG[C/T]GGGATTCCAGGAGGC | 7088 |
rs62576160 | snp | A/T | 0.0850919 | 0.187897 | intron-variant | TLE1 | GRCh38.p7 | 9:81609288 | CGGGGTTTCGCCACA[A/T]TGGCCAGGCTGGTCT | 7088 |
rs62576161 | snp | C/T | 0.329084 | 0.237162 | intron-variant | TLE1 | GRCh38.p7 | 9:81612136 | CCTCCTTCCCCAGAG[C/T]GAATGCATCTCCAGG | 7088 |
rs62576162 | snp | A/G | 0.345704 | 0.230956 | intron-variant | TLE1 | GRCh38.p7 | 9:81615324 | ACAGAGTGAGACTCC[A/G]TCTCAGAAAAAAAAA | 7088 |
rs62576163 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | TLE1 | GRCh38.p7 | 9:81623046 | CATTGTTGTTCTTGA[A/T]ATAAGCAAACAGTTC | 7088 |
rs62576164 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623547 | ACTTAGGGAGGCCGA[A/G]GCAGGCAGATCGCCT | 7088 |
rs62576165 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TLE1 | GRCh38.p7 | 9:81626529 | AACATGGACAAAGTT[A/G]AAAATCTGTCCACTG | 7088 |
rs62576166 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81635560 | AAACTTATTTTTGAT[A/G]AGACAGTAAAAATGA | 7088 |
rs62576167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638172 | GACGGGGGAGTTTAC[A/G]CTTAGACTGCATGAG | 7088 |
rs62576168 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641351 | GTGAATGGCCTCTCA[C/T]GTAAAGAGGGGCAAG | 7088 |
rs62576169 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643638 | GTCCCAGACTCAAGC[A/G]ATCCTCCCACCTCAA | 7088 |
rs62576170 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643641 | CCAGACTCAAGCAAT[C/T]CTCCCACCTCAACCT | 7088 |
rs62576193 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643653 | AATCCTCCCACCTCA[A/G]CCTCCTGAGTAGCTG | 7088 |
rs62576194 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643659 | CCCACCTCAACCTCC[C/T]GAGTAGCTGGGACTA | 7088 |
rs62576195 | snp | C/T | 0.427879 | 0.175668 | intron-variant | TLE1 | GRCh38.p7 | 9:81645177 | CCAGCCTGACCAACA[C/T]GGAGAAACCCTGTCT | 7088 |
rs62576196 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81645365 | AGAGAAACTCCGTCT[A/C]CAAAAAAAAAAAAAT | 7088 |
rs62576198 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TLE1 | GRCh38.p7 | 9:81661000 | CCTGGCGTGGTGGCA[C/T]GTGCCTGTAGTTCCA | 7088 |
rs62576199 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81664251 | AAGACACTGCCTCTA[A/C]CAAAAAAAAAAAAAA | 7088 |
rs62576200 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | TLE1 | GRCh38.p7 | 9:81664800 | CAGCGTACACGAGGA[C/T]GGTCTTGTGCTTGTT | 7088 |
rs62576201 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667066 | TTGGTTTGGAGTTTG[G/T]AGTTTTGATTAAGCC | 7088 |
rs62576202 | snp | A/C | 0.288386 | 0.247035 | intron-variant | TLE1 | GRCh38.p7 | 9:81673112 | ATCCCGACTCTACTA[A/C]AAATACAAAAATCAG | 7088 |
rs62576204 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81678556 | CAGTGGCTCACGCCT[A/C/G]TTAATTCCAGCACTT | 7088 |
rs62576222 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683989 | TCCTCCAATAAACCC[A/C]GCACCAGCATATAGC | 7088 |
rs62576223 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688657 | AAACAAATCCAGACG[G/T]ACTGCTTTTCTTTGC | 7088 |
rs62576224 | snp | A/G | 0.0298908 | 0.118541 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688900 | AGCGACGGATGACGA[A/G]GCGGGGAAAGTGCGG | 7088 |
rs62578583 | snp | A/C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583259 | GAGAGAGAGAGAGAA[A/C/T]GAAAGAAAGAGAGAA | 7088 |
rs62578585 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585351 | CTGAAACAGACATTG[A/C]TGTGCTCTGAAGGGC | 7088 |
rs62578587 | snp | A/G | 0.0858192 | 0.188533 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586264 | CTTTGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 7088 |
rs62578588 | snp | C/T | 0.137867 | 0.223442 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590592 | GGCACATTAAGGAGA[C/T]AGAAAGTCTCGGGTG | 7088 |
rs62578589 | snp | A/G | 0.135825 | 0.222405 | intron-variant | TLE1 | GRCh38.p7 | 9:81591428 | CATCCTCTATGTTTC[A/G]GTCTTCGTTATGCTG | 7088 |
rs62578590 | snp | C/T | 0.127599 | 0.217986 | intron-variant | TLE1 | GRCh38.p7 | 9:81592185 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 7088 |
rs62578591 | snp | A/G | 0.12932 | 0.218944 | intron-variant | TLE1 | GRCh38.p7 | 9:81592284 | AACGGCGTAAACCCC[A/G]GAGGCGGAGCCTGCA | 7088 |
rs62578607 | snp | C/T | 0.132751 | 0.2208 | intron-variant | TLE1 | GRCh38.p7 | 9:81593994 | CTGACCAATGAGGTG[C/T]AAGAAGAAGCTGTTG | 7088 |
rs62578608 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604117 | AAATTCTTAATAAGA[A/C]TTGCATGCATTTCTC | 7088 |
rs62578609 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81606788 | AATTAAAAAAAAAAC[A/C]ATATATATATATATA | 7088 |
rs62578610 | snp | C/T | 0.204189 | 0.245767 | intron-variant | TLE1 | GRCh38.p7 | 9:81607903 | ATTGCTACTGATTCC[C/T]AGTGTAGACAAAAAC | 7088 |
rs67600750 | in-del | -/ATCC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584992 | CCATCCATCCATCCA[-/ATCC]TCCATCCATCTATGC | 7088 |
rs67822293 | in-del | -/T | 0.35894 | 0.225016 | intron-variant | TLE1 | GRCh38.p7 | 9:81618988 | CCAACCAGACAAACC[-/T]AGTACATGCAGGTTA | 7088 |
rs67924421 | in-del | -/CCC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632473 | TTAAATGTTCAGTAT[-/CCC]TTTTTTTTTTTTTTT | 7088 |
rs68097268 | snp | C/T | 0.344592 | 0.231414 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686272 | TAGGCATAGGCTGTG[C/T]CATCTTTGCCAACTC | 7088 |
rs68120095 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637645 | ACAATGAAAGTTTCT[-/T]TTTTTTTTTTTTTTT | 7088 |
rs71359015 | in-del | -/AAGA | 0 | 0 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583269 | AGAACGAAAGAAAGA[-/AAGA]GAGAAAGGGAAAGAG | 7088 |
rs71359018 | in-del | -/A | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81594557 | TTAAAAAAAAAAAAA[-/A]TTATGCACATTCTAC | 7088 |
rs71359019 | in-del | -/TG | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81656259 | CTCCTCGAAAGCATG[-/TG]GGCAAGGCTTTCCTT | 7088 |
rs71359020 | in-del | -/GTGTGT | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81662406 | TGTGTGTGTGTGTGT[-/GTGTGT]TTAAAGGGCCAGGAG | 7088 |
rs71359022 | in-del | -/C/CA | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81677245 | CGTCTTCCCCCCCCC[-/C/CA]AAAAAAAAGACCTTA | 7088 |
rs71359023 | in-del | -/A | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81677575 | AAAAAAAAAAAAAAA[-/A]GTAAACAACTCAGGT | 7088 |
rs71490564 | multinucleotide-polymorphism | AAG/GGA | 0 | 0 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583239 | AAAAAAAAAAAAAAA[AAG/GGA]GAGAGAGAGAGAGAG | 7088 |
rs71496083 | in-del | -/TG | 0.5 | 0 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587946 | GTGTGTGTGTGTGTG[-/TG]ATCCCGCCAGTGTCT | 7088 |
rs71496084 | in-del | -/AT | 0.490175 | 0.0693959 | intron-variant | TLE1 | GRCh38.p7 | 9:81632134 | TGGAATGGCAAAACA[-/AT]ATAAGGCTTCCTCCA | 7088 |
rs71498441 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81597107 | CAGCCAGCCTGCAGT[C/T]TAGAATGTGTCTGTT | 7088 |
rs71498442 | snp | G/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81604827 | ACTGTGCCTCCCCGG[G/T]TCCATGGGAAACTCA | 7088 |
rs71498443 | snp | A/T | 0.491629 | 0.0641526 | intron-variant | TLE1 | GRCh38.p7 | 9:81606777 | ACTTAAAGTATAATT[A/T]AAAAAAAAACCATAT | 7088 |
rs71498444 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81615168 | GCGTGTACACCCTCT[C/T]TAATGTATGGTGGTA | 7088 |
rs71498445 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81615326 | AGAGTGAGACTCCGT[C/T]TCAGAAAAAAAAAAA | 7088 |
rs71498446 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81615348 | AAAAAAAAAAAGAAT[C/T]TCAGAAGTTTGAACC | 7088 |
rs71498447 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81615386 | AACTGGGAAGTTTCA[A/G]AGAGCTGTGTGGCAA | 7088 |
rs71498448 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81615532 | GGCAAAACCCCATCT[C/T]TACTAAAAATACAAA | 7088 |
rs71498449 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81631234 | CCAATAACCCTCCCT[C/T]CACCCACTCCAATGA | 7088 |
rs71699706 | in-del | -/TCATCCCGCC/TGTCATCCCGCC/TGTGTCATCCCGCC | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587924 | GTGTGTGTGTGTGTG[lengthTooLong]TGTGTGTGTGTGTGT | 7088 |
rs71885823 | in-del | -/TTAAA | 0.371785 | 0.218331 | intron-variant | TLE1 | GRCh38.p7 | 9:81629298 | TAATGCAATTTATCC[-/TTAAA]TTAATTAAAATATCT | 7088 |
rs71968376 | in-del | -/AA | | | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583239 | AAAAAAAAAAAAAAA[-/AA]GGAGAGAGAGAGAGA | 7088 |
rs72316626 | in-del | -/AGATT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663350 | AAGATCATAGAGCAA[-/AGATT]GAAGCCACATATTCC | 7088 |
rs72410619 | in-del | -/TGAGCAC | 0.174932 | 0.238463 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590168 | AGAACAGCTCTGGTG[-/TGAGCAC]TGACTTCTGAAGGGA | 7088 |
rs72450364 | in-del | -/TG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656258 | TCTCCTCGAAAGCAT[-/TG]GGGCAAGGCTTTCCT | 7088 |
rs72747215 | snp | A/T | 0.0232847 | 0.105357 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583488 | ACTCACAATTCCTAG[A/T]CTTGAGCTCCCAGTA | 7088 |
rs72747231 | snp | C/G | 0.0693955 | 0.172864 | intron-variant | TLE1 | GRCh38.p7 | 9:81591103 | TACCGAGCAATCATA[C/G]CACCATGTTCTCTAA | 7088 |
rs72747234 | snp | G/T | 0.130008 | 0.219321 | intron-variant | TLE1 | GRCh38.p7 | 9:81592405 | CCCAACATGTTTTAT[G/T]TCCCTGAAAAATGCT | 7088 |
rs72747240 | snp | A/C | 0.0876345 | 0.190099 | intron-variant | TLE1 | GRCh38.p7 | 9:81596615 | GAAAGAGGAATGTAT[A/C]AACAGATAGTGAGCA | 7088 |
rs72747245 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81611407 | AAGAAAATGAATGAA[A/G]AGGCTTCTGTGAACC | 7088 |
rs72747249 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612643 | CACGGTTGGGCCAGC[A/C]AAACCGCTGTTTCAG | 7088 |
rs72747252 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | TLE1 | GRCh38.p7 | 9:81615889 | TACAACCCTCAAGCA[A/G]CAAAACCCCCACATT | 7088 |
rs72747253 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | TLE1 | GRCh38.p7 | 9:81619930 | TCACTATGGAAGACA[C/T]TGAGCTCTGCCTTGA | 7088 |
rs72747266 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | TLE1 | GRCh38.p7 | 9:81630760 | CACTTTATTAAATAG[A/G]TAAGTACTATAATAT | 7088 |
rs72747274 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81644285 | CAAATGTTCATAGCA[C/G]CATTATTCAAAATAG | 7088 |
rs72747286 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81660722 | TGCCCAGCTACATGT[A/G]TGTTTTAACTGAGCA | 7088 |
rs72747288 | snp | G/T | 0.151001 | 0.229563 | intron-variant | TLE1 | GRCh38.p7 | 9:81660793 | ACTCTAGTGTATTCT[G/T]CGACTTTTAAATTCA | 7088 |
rs72747292 | snp | C/G | 0.093777 | 0.195178 | intron-variant | TLE1 | GRCh38.p7 | 9:81666882 | TCAGCACTTTTGAGA[C/G]CAAGGTAAGAGGATC | 7088 |
rs72747296 | snp | A/C | 0.0948562 | 0.196037 | intron-variant | TLE1 | GRCh38.p7 | 9:81672763 | TTTCCATGTTACATT[A/C]GAAAGAAAAACTCTG | 7088 |
rs72747300 | snp | C/T | 0.172351 | 0.237636 | intron-variant | TLE1 | GRCh38.p7 | 9:81676856 | CAAGTCAATGGAATG[C/T]GTGCTGACATTTCAT | 7088 |
rs72747302 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | TLE1 | GRCh38.p7 | 9:81682445 | GAAGACAAATCACAT[C/T]GAAAACTGTTCATTA | 7088 |
rs72749004 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81684551 | ACACACTTGCTTAAT[A/G]AAAGTCTTTGAATAT | 7088 |
rs72749005 | snp | A/C | 0.162253 | 0.234095 | intron-variant | TLE1 | GRCh38.p7 | 9:81685382 | AGCCCTTTCAAGAGG[A/C]TAAATCTATACAGGT | 7088 |
rs72749007 | snp | A/T | 0.113334 | 0.209338 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687584 | AGTTTGCCCTTCACT[A/T]TGGGGAGGGGGAAAG | 7088 |
rs72749008 | snp | C/G | 0.0652144 | 0.168387 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688005 | CCGCTCGGTATAGAC[C/G]TCAAGTAGGAAGGAG | 7088 |
rs72749010 | snp | A/G | 0.0652144 | 0.168387 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688035 | GCCCAAAGGGAGGGA[A/G]AAAATTAAGAGTTTC | 7088 |
rs72749012 | snp | G/T | 0.0652144 | 0.168387 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691454 | CATTGTAGCTTTGTG[G/T]TGTTCTCATTAAGTA | 7088 |
rs73468030 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587582 | TGATCTGTTTGTCCA[C/G]CCACTACCATCCTAG | 7088 |
rs73468033 | snp | C/T | 0.270621 | 0.249148 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589757 | GCTACTTATGGAGTT[C/T]TAAAAAAAGAAAAAA | 7088 |
rs73468050 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81598138 | ATCAAAAATCTGATC[A/G]TGTCAAAAACCTTCA | 7088 |
rs73468062 | snp | A/T | 0.11228 | 0.208646 | intron-variant | TLE1 | GRCh38.p7 | 9:81608230 | ACCGGTTTGCCCCTT[A/T]TCCACTCACCAATCA | 7088 |
rs73468065 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | TLE1 | GRCh38.p7 | 9:81608551 | GTGACATGCAAGTGA[C/T]GTACTGATAAAAGCT | 7088 |
rs73468074 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | TLE1 | GRCh38.p7 | 9:81610083 | ATTTATAGAAAGTGT[G/T]AACACTCCTCAGGAA | 7088 |
rs73468084 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | TLE1 | GRCh38.p7 | 9:81613299 | TTGTAGGGCAATTGC[A/G]TCACAACATTAACAG | 7088 |
rs73468099 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | TLE1 | GRCh38.p7 | 9:81620087 | AGACCTTATTCAAAA[A/T]TTGAGAACGCAAAGA | 7088 |
rs73470148 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | TLE1 | GRCh38.p7 | 9:81648366 | TTCTTTAGGAGAAGG[C/G]GAAAAACTGTAAGAA | 7088 |
rs73470156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653275 | ATAAACTTTCCACCC[G/T]GCGTGAAGATGCATT | 7088 |
rs73470160 | snp | A/G | 0.106278 | 0.204558 | intron-variant | TLE1 | GRCh38.p7 | 9:81666714 | CGGGAAGCGGAGGTT[A/G]CAATGAGCCAAGATC | 7088 |
rs73470176 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | TLE1 | GRCh38.p7 | 9:81673850 | AAGCCAAAGAGCTGA[A/G]AAAGACAACTATGTG | 7088 |
rs73647835 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | TLE1 | GRCh38.p7 | 9:81613684 | CTTGTGAGCGAGAAA[G/T]GTTGACCTTTCCTCT | 7088 |
rs73647836 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TLE1 | GRCh38.p7 | 9:81630769 | AAATAGATAAGTACT[A/G]TAATATTTTAGGCAC | 7088 |
rs73647837 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | TLE1 | GRCh38.p7 | 9:81637822 | ATCTAAGTGTCCATC[A/G]TCTGGCACAAGCTTG | 7088 |
rs73647838 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | TLE1 | GRCh38.p7 | 9:81647697 | AGGTAGACGGTATTA[C/T]CATCTACAGATAGGG | 7088 |
rs73647839 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | TLE1 | GRCh38.p7 | 9:81651086 | CCATTGTCTGTGGCC[A/G]TCATTGGACTATGGC | 7088 |
rs73647840 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | TLE1 | GRCh38.p7 | 9:81653543 | ATCCACCCCTTCAAG[A/G]ACAGCATTAAGACAA | 7088 |
rs73647841 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | TLE1 | GRCh38.p7 | 9:81654174 | TTCCCCAGGTTATGT[C/T]ACTAATACTTATCTT | 7088 |
rs73647842 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81655870 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAACAA | 7088 |
rs73647843 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | TLE1 | GRCh38.p7 | 9:81662184 | TTTGAGAAAGTTAAC[A/G]TTTGCCCTCCTAATA | 7088 |
rs73647844 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | TLE1 | GRCh38.p7 | 9:81664176 | GCCTATAATCCCACC[A/G]TTTTGGGCGGGATGG | 7088 |
rs73647845 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | TLE1 | GRCh38.p7 | 9:81664856 | GCGGAGTTCCTGTTG[A/G]AGTCTAGGCCTGAGA | 7088 |
rs73647872 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | TLE1 | GRCh38.p7 | 9:81669447 | ACTAATGCTTATTCA[C/G]GTTTTAGATCATCAG | 7088 |
rs73647873 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | TLE1 | GRCh38.p7 | 9:81673476 | CTAGAAGTCCAAGAG[C/T]AGGGGTAGAGTTTTA | 7088 |
rs73647874 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | TLE1 | GRCh38.p7 | 9:81673789 | ACTCTAATGTTGTCA[C/T]TGGAAAAGCTTACTG | 7088 |
rs73647876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81679964 | TTTAACTACCACTCA[A/G]GATGATTTATTTAAA | 7088 |
rs73650843 | snp | A/G | 0.0596104 | 0.162024 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590211 | GGCGGGGGAGCTGAG[A/G]AGAGACACATGGGTA | 7088 |
rs73650844 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | TLE1 | GRCh38.p7 | 9:81597701 | TCTGGTGTCAGAATC[A/G]AAAAGAATAAAGCCC | 7088 |
rs73650845 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | TLE1 | GRCh38.p7 | 9:81598354 | CTCCCAAGTACACGC[C/T]GCTTCCTCCCTCCCT | 7088 |
rs73650846 | snp | A/C | 0.0479149 | 0.147179 | intron-variant | TLE1 | GRCh38.p7 | 9:81600875 | GAGGAGCAAGTGTGC[A/C]CTTCACTTGAGCTGG | 7088 |
rs74200531 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632217 | CCCAGCTATAATTTT[C/T]TGTCCCCCCAATCCC | 7088 |
rs74213360 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671664 | AAAAAAAAGAAAAAA[-/AA]TCTATATACTCAGAA | 7088 |
rs74332268 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TLE1 | GRCh38.p7 | 9:81641492 | GCACACAGAAAATGA[C/T]GCATGGGCAACCTAA | 7088 |
rs74387586 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81684163 | TAAAAAAAAAAAAAA[A/G]GATTAAACCGCCTAG | 7088 |
rs74436915 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | TLE1 | GRCh38.p7 | 9:81663544 | CCAACAAAGGGACTA[C/T]AGAAAGTGCCTCTCA | 7088 |
rs74534857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589769 | GTTTTAAAAAAAGAA[A/G]AAAACAAGTAACTTT | 7088 |
rs74536663 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | TLE1 | GRCh38.p7 | 9:81632180 | TTACTTATCTGTACT[C/G]TGTGTGTAGAATATT | 7088 |
rs74611265 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81659703 | GTTAGCCCTCATCAT[C/T]CAAAAATTAGGGTTT | 7088 |
rs74697566 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | TLE1 | GRCh38.p7 | 9:81662351 | CGGTGTTAGTATTAG[C/T]GTGCCTGTTTTGTGT | 7088 |
rs74699801 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | TLE1 | GRCh38.p7 | 9:81675429 | AATTCATCTACACTC[C/T]ATTGGCAGCTGCAGT | 7088 |
rs74710297 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586499 | CATTGAAAAGGTACA[A/G]TAAAAATATAGTATT | 7088 |
rs74720924 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81671742 | TCCATTTAATTCATA[A/C]ATATCATAGCATCTA | 7088 |
rs74757174 | snp | C/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81613906 | GACCCCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 7088 |
rs74838128 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | TLE1 | GRCh38.p7 | 9:81625659 | CTCAGAGAGCACCCA[A/G]TGGCGTCAAAAGAAA | 7088 |
rs74891619 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670728 | AGAAAAAAAAAAATT[A/T]AAAAAAAAAAATCAC | 7088 |
rs74984665 | snp | A/C | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81655852 | AGCAAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 7088 |
rs75189294 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81644192 | TCTGGCTGTTGCTCA[A/G]AAAGTTACCATAGAC | 7088 |
rs75270768 | snp | A/C | 0.0785177 | 0.181917 | intron-variant | TLE1 | GRCh38.p7 | 9:81660341 | GACAAAGGCTGTTCA[A/C]AAAAAAAAAAAAACA | 7088 |
rs75440932 | snp | A/T | 0.039522 | 0.134904 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690987 | CAGCAGAAAACCGTC[A/T]GTATTGCCGCATTTA | 7088 |
rs75459535 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | TLE1 | GRCh38.p7 | 9:81639318 | CAATCCTCCTGCCTC[A/G]GCCTTCCAAAGTGCT | 7088 |
rs75676414 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81642291 | ATTCTGGATTTTTTT[C/T]AGATTTTTAAATATT | 7088 |
rs75699815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604366 | AAACCATGGCCCACA[A/G]GAGAGGGCTGAAGCG | 7088 |
rs75707534 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81685411 | GTGAAAAAGTAAACT[C/G]AAGTCTTAATTCCTA | 7088 |
rs75723642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81595680 | AAAAATCAGCCGGGT[A/G]TGGTGGCGGGCGCTT | 7088 |
rs75753435 | snp | A/C | 0.106987 | 0.205054 | intron-variant | TLE1 | GRCh38.p7 | 9:81597300 | AAAAGCCAAGTGAAG[A/C]TACGTTGAATTGAGG | 7088 |
rs75917762 | in-del | -/AAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664264 | TACCAAAAAAAAAAA[-/AAA]CTTAATTAGGGATAC | 7088 |
rs76066110 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81657214 | TGGGACAAATATTAA[C/T]CCTTTATCAGAGTTT | 7088 |
rs76102415 | snp | G/T | 0.00777751 | 0.061873 | intron-variant | TLE1 | GRCh38.p7 | 9:81593279 | AGGAGTATGCACTTT[G/T]GGAAAAACGATTGGA | 7088 |
rs76149927 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81680580 | CCAGGACAAAAACCA[A/G]CCACTGGCCCACTGC | 7088 |
rs76178854 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | TLE1 | GRCh38.p7 | 9:81635797 | TAGAGAAAACACCAT[A/C]TTAAGGCAGAAATCA | 7088 |
rs76214884 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | TLE1 | GRCh38.p7 | 9:81635367 | TCCCAAATGCCTTTT[A/C]CATGACTGCACTTTG | 7088 |
rs76239633 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622818 | CTGTAAAACTGACTC[-/A]AAACAAGGCAGCAGA | 7088 |
rs76242276 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81660822 | CAAGATATGGCCGGG[C/T]GTGGTGGCTCACGCC | 7088 |
rs76247426 | snp | A/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81684392 | CCAATTACATTATTA[A/T]TAAAAGGCCCTGAAA | 7088 |
rs76317077 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81682683 | AAACCACCAGGCTCA[C/T]ATCAACTTGCTGTTT | 7088 |
rs76353027 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81607783 | ACCAGGTAGTAACTA[A/G]TTCATGGGTACTCAA | 7088 |
rs76416936 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81632044 | GCAGTGAGCCGAGAT[A/T]GTGCTACTGCACCCC | 7088 |
rs76501258 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605814 | CGGCAAAAAAAAAAA[-/AA]CTACCATTAGAGTGA | 7088 |
rs76512220 | snp | A/T | 0.119281 | 0.213102 | intron-variant | TLE1 | GRCh38.p7 | 9:81597741 | CACAGATGTAAAACA[A/T]GAATGATATAAAAAC | 7088 |
rs76625462 | snp | A/C | 0.121717 | 0.214577 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589844 | ATTCCATTTTGCTCA[A/C]CTACACTACCCAGCA | 7088 |
rs76630120 | snp | A/G | 0.251014 | 0.249998 | intron-variant | TLE1 | GRCh38.p7 | 9:81618021 | CAAAAGCAAGACTCC[A/G]TCTCAAAACAACAAC | 7088 |
rs76698434 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | TLE1 | GRCh38.p7 | 9:81619843 | CAGTAGAGTGATCTC[A/C]TCTACAGAATTTAAA | 7088 |
rs76722895 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | TLE1 | GRCh38.p7 | 9:81601017 | GATTTCTCAGTCTAC[A/G]CAGTCGTGTGAGCCA | 7088 |
rs76767779 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81649189 | TTTTCTTAAATACCG[A/G]TACTCTATGTAAGTT | 7088 |
rs76791402 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81649714 | TGCATTTACTCTGCG[C/T]GCAGCTGCTGCTTGT | 7088 |
rs76822827 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81637385 | AGATGAACTGGGTAG[C/T]AGATTCTGATATCTT | 7088 |
rs76867202 | snp | A/C/T | 0.0414363 | 0.137845 | intron-variant | TLE1 | GRCh38.p7 | 9:81663013 | CCACCACGTGCAGCT[A/C/T]ATTTTTGCATTTTTA | 7088 |
rs76917265 | in-del | -/TAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684390 | GCCCAATTACATTAT[-/TAA]TAAAAGGCCCTGAAA | 7088 |
rs76928796 | snp | A/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81683225 | CCCCATCACTGCATT[A/T]TTTTTTTTTTTTTAG | 7088 |
rs76955370 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81647931 | ACTATTAATATTTTT[A/T]AAAATGCAATTAGCT | 7088 |
rs77017278 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81616271 | AGGTGACCAACACCA[C/T]GTTATAAATGAGCAA | 7088 |
rs77020096 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670726 | TCAGAAAAAAAAAAA[A/T]TAAAAAAAAAAAATC | 7088 |
rs77020677 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81645791 | AAATGCTTGAGGGGA[C/T]AGATACCCCATTCTT | 7088 |
rs77035433 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | TLE1 | GRCh38.p7 | 9:81634801 | TAGCCATACTCTCAA[A/C]CTGTCACCAGGTAAC | 7088 |
rs77061048 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | TLE1 | GRCh38.p7 | 9:81643981 | ACAAAAACTATACAG[A/G]TTTTGATTGAAAAGA | 7088 |
rs77065384 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | TLE1 | GRCh38.p7 | 9:81596906 | TTCATGCACTTTTCT[A/G]TATGTGTATGGTATT | 7088 |
rs77103586 | snp | A/T | 0.0670745 | 0.170406 | intron-variant | TLE1 | GRCh38.p7 | 9:81604775 | CTCATCCACCTGCAC[A/T]TGGATCCCTCAAGCT | 7088 |
rs77127780 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TLE1 | GRCh38.p7 | 9:81647649 | AAACTGCAGTTCAAG[A/G]AGTCAGGACCACATG | 7088 |
rs77141162 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81601603 | TGCTACAGTGCCAGA[A/G]AAAAAAAAAAAAAGT | 7088 |
rs77183706 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81673294 | AAAAAAAAAAAAAAA[A/C]CAGACTGCCAACAAG | 7088 |
rs77252633 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81652404 | GTAGAAGGGTTTAAA[C/T]GCAGAATTTCTCAAC | 7088 |
rs77306737 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | TLE1 | GRCh38.p7 | 9:81624769 | GTATGTAAGTTTTCA[C/T]TTAAAATTAAAAAAA | 7088 |
rs77315202 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81653054 | CCATAAATTTACTTT[A/G]GGAGGCATGAGAATG | 7088 |
rs77346095 | snp | C/G | 0.249603 | 0.25 | intron-variant | TLE1 | GRCh38.p7 | 9:81622255 | TCTGTGCAGCATCCA[C/G]GGCAGGGCTGTATCT | 7088 |
rs77396335 | snp | A/C | 0.154993 | 0.231244 | intron-variant | TLE1 | GRCh38.p7 | 9:81615819 | AGGGGAAAAAGTAAA[A/C]CCTGAATGGTGACAA | 7088 |
rs77456510 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81673324 | GTCCTTTTTTTTTTT[C/T]CTCCTTTTAAGCCTA | 7088 |
rs77496252 | in-del | -/CCCTTTTTTTTTTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632473 | TTAAATGTTCAGTAT[-/CCCTTTTTTTTTTTT]TTTTTTTTTACCATA | 7088 |
rs77547622 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81613272 | GAGGGTGGCCCTACG[G/T]ACATTTCATATTTGT | 7088 |
rs77564524 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81584645 | ATCATGCCCTAAGGA[C/T]TGGTCCATGATATGA | 7088 |
rs77582848 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TLE1 | GRCh38.p7 | 9:81670059 | GTCTCCATGACAACG[C/T]TGGCCAACCCTGCAA | 7088 |
rs77638655 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598556 | GAACACCACAAGCTG[C/T]CTACTGTTACCTAAT | 7088 |
rs77679800 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81658187 | AAAGTGCTAGGATTT[A/G]TAATCCTAGCATGAG | 7088 |
rs77764293 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81607648 | TTTATCCACTCACCA[A/G]TCAGTAGAACACAAC | 7088 |
rs77783802 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643532 | TGAGCCACCGCACCC[A/G]GCCCTTTGTTTTGTT | 7088 |
rs77798267 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | TLE1 | GRCh38.p7 | 9:81664623 | TCCCAGCACTTTTGC[C/G]GGGCTGAGGCAGGAG | 7088 |
rs77830683 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686381 | TAAATCCCTGCCAAA[A/G]TATGTCAAGTAGCTA | 7088 |
rs77839901 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | TLE1 | GRCh38.p7 | 9:81661937 | ACTGATGACATTAAA[C/T]TGGTAGCGCTGTCTT | 7088 |
rs77880430 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TLE1 | GRCh38.p7 | 9:81646880 | AAAATCAGATATTTG[C/T]CTATGGAGAAGGAAT | 7088 |
rs78032891 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81682254 | CGAGATTCCATCTCA[A/C]AAAAAAAAAAAAAGC | 7088 |
rs78052752 | snp | C/T | 0.127254 | 0.217792 | intron-variant | TLE1 | GRCh38.p7 | 9:81584969 | GCACTCATCCACCCA[C/T]CCATCCATCCATCCA | 7088 |
rs78117441 | snp | A/G | 0.0345262 | 0.126772 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587512 | GGTAGGGGGAGGGTC[A/G]TGAAGGAGGAGGTGG | 7088 |
rs78180759 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | TLE1 | GRCh38.p7 | 9:81635552 | CCAATATAAAACTTA[C/T]TTTTGATGAGACAGT | 7088 |
rs78227178 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | TLE1 | GRCh38.p7 | 9:81638110 | AGAACACCTGATACT[A/G]CATACACAGAGACAA | 7088 |
rs78229974 | snp | C/G | 0.106987 | 0.205054 | intron-variant | TLE1 | GRCh38.p7 | 9:81597299 | AAAAAGCCAAGTGAA[C/G]ATACGTTGAATTGAG | 7088 |
rs78237454 | snp | A/C | 0.119281 | 0.213102 | intron-variant | TLE1 | GRCh38.p7 | 9:81597427 | AGGCAACAAAAAATA[A/C]AAAATTCTTAAGTCA | 7088 |
rs78254631 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | TLE1 | GRCh38.p7 | 9:81665608 | GTGAGGCAGATTGCA[A/G]GGGCCTGCATCTCCG | 7088 |
rs78255581 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81620999 | AGGCACAAAGGAAGC[A/G]GTGGGATTAACAGCA | 7088 |
rs78293310 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81632045 | CAGTGAGCCGAGATA[C/G]TGCTACTGCACCCCA | 7088 |
rs78324828 | snp | G/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81599033 | CTAACTTGAGCCTCA[G/T]TTCCCCATTTTTACA | 7088 |
rs78458688 | snp | C/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81663624 | CGCACAGAATAGACT[C/T]TTTTTTTTTTTTTTT | 7088 |
rs78471932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620762 | GACTTTGCAATCAAA[C/G]CATCCAAAGCTAGGT | 7088 |
rs78504317 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81615728 | AAAAAAAAAAAAAAA[A/G]AGAAGAAGAAGAAGA | 7088 |
rs78585658 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81653403 | AGTCAGTTTCATAGA[C/T]TACTCATATAAAGAG | 7088 |
rs78632358 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588724 | CAGTTCTGCATGCTG[A/G]GAGGAAGGTGGTGGG | 7088 |
rs78633358 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81637052 | TTCCCCTCCCATAAA[C/T]CCAAGCTAGCTTTCA | 7088 |
rs78642889 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81676784 | GGGCTGGAGTTCCCA[C/G]GGTGCGGCCAGGTTT | 7088 |
rs78654671 | snp | A/C | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81645367 | AGAAACTCCGTCTCC[A/C]AAAAAAAAAAAATAA | 7088 |
rs78656704 | snp | A/C | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81655854 | CAAGACCCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 7088 |
rs78685355 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81635025 | CCCATTTCCCAGAAG[A/G]AATGAAGGCTCAAAG | 7088 |
rs78707453 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TLE1 | GRCh38.p7 | 9:81671910 | ATCTCCTCAGTAGCT[A/G]TGCAGAGACATTGGC | 7088 |
rs78729715 | snp | C/G/T | 0.00398731 | 0.0445001 | intron-variant | TLE1 | GRCh38.p7 | 9:81617031 | AACAGCTGAATTTCT[C/G/T]GAGGGATGAAATCTT | 7088 |
rs78730461 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81653767 | TCCACAGGAAAAAAA[A/T]TTAATTTGGGGGTTG | 7088 |
rs78747387 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | TLE1 | GRCh38.p7 | 9:81613822 | CTACGCCAAGTTAGA[A/G]AGATGACCACCCAGA | 7088 |
rs78784008 | snp | C/G | 0.127254 | 0.217792 | intron-variant | TLE1 | GRCh38.p7 | 9:81631709 | TCAATAGATTTAAAA[C/G]GCATAACAGCCTAAA | 7088 |
rs78796872 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | TLE1 | GRCh38.p7 | 9:81639243 | AGCTTGGCTAATTTT[G/T]TTTACACAGATGGGG | 7088 |
rs78808153 | snp | A/G | 0.110167 | 0.207236 | intron-variant | TLE1 | GRCh38.p7 | 9:81621975 | ATAGAGAAGCTCTAA[A/G]TAATGTCTTTACCAC | 7088 |
rs78808254 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81648272 | AGTAACACTGTCTCC[A/C]AAAAAAAAAAAAACC | 7088 |
rs78850209 | snp | C/T | 0.118933 | 0.212888 | intron-variant | TLE1 | GRCh38.p7 | 9:81604929 | TGTCTCCCTATCACC[C/T]ACTGCTCTGCCTCAA | 7088 |
rs78853872 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81650347 | AGAGTTTTGCCATCA[C/T]GAAATTATATGTCGT | 7088 |
rs78892898 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TLE1 | GRCh38.p7 | 9:81659970 | ATAACGCCAATAAAC[A/G]CACTCTTCTCTAGGC | 7088 |
rs78989430 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81641423 | TCCAGCCACTTGAAG[A/T]CAATAACAAAAACTA | 7088 |
rs78990820 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TLE1 | GRCh38.p7 | 9:81635453 | CATTGCTCTTATACA[C/T]TATATTTAAAAGCAC | 7088 |
rs79006477 | in-del | -/AA | 0.305186 | 0.243833 | intron-variant | TLE1 | GRCh38.p7 | 9:81598726 | TGGTAGCAGTTTCCT[-/AA]AAGGGGGAAAGGCAG | 7088 |
rs79025567 | in-del | -/TAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666783 | GTCTCACAAAATAAA[-/TAAA]TAAATAAATAAATAA | 7088 |
rs79050052 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664721 | TAAGAAAAAAAAAAA[A/T]AAGTGAGGTACCTTT | 7088 |
rs79157085 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583688 | GGAAAACCACTTATT[G/T]GTACTAAAGCCTTTA | 7088 |
rs79223669 | in-del | -/A | 0.344815 | 0.231323 | intron-variant | TLE1 | GRCh38.p7 | 9:81685196 | CCTGACTATTGCTTC[-/A]ATGCAGCCCCAAAGC | 7088 |
rs79238155 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660355 | ACAAAAAAAAAAAAA[A/C]AAAATCATACGTTGG | 7088 |
rs79246784 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81655369 | CCACCTCAAAAAATA[A/T]AAAAAATAAAGAAGG | 7088 |
rs79258562 | snp | A/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81673270 | AAGAGCGAGACTTCA[A/T]TTAAAAAAAAAAAAA | 7088 |
rs79294665 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | TLE1 | GRCh38.p7 | 9:81657582 | AAATGAACTTGTAAA[A/C]CTTTAATAATATTAA | 7088 |
rs79314281 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81622319 | AAATGGGGCACAGAG[A/G]CTGGGTGTGCTGACC | 7088 |
rs79360952 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | TLE1 | GRCh38.p7 | 9:81611358 | TGGCTTCTCAGACAT[C/T]TTTTCCTAAGGTTTA | 7088 |
rs79403151 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | TLE1 | GRCh38.p7 | 9:81656870 | TCTAAAAGGAATCCC[C/T]AGATGTGAAACTGCT | 7088 |
rs79491036 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81651931 | GAGTAGGCAAAATAC[A/C]AAGACCCCGGTCTGT | 7088 |
rs79522428 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | TLE1 | GRCh38.p7 | 9:81651588 | TGAAAGAGGCACAAG[A/C]AAGAACAAGAGCCAA | 7088 |
rs79534805 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81644039 | ATGCAAATCAAAAAC[A/G]GGAGATGCGGCCTCA | 7088 |
rs79580646 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590615 | CTCGGGTGACACCAG[A/G]CATAGTAATAAGACT | 7088 |
rs79621193 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81660354 | CACAAAAAAAAAAAA[A/C]CAAAATCATACGTTG | 7088 |
rs79709264 | snp | A/G | 0.121717 | 0.214577 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589899 | CACTGTCACCCACAC[A/G]CAGGGACCGGGCCCG | 7088 |
rs79724272 | snp | C/G | 0.0652144 | 0.168387 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689955 | TTGGCACTGATGATG[C/G]GAAGGTCGGTGGGAA | 7088 |
rs79745040 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TLE1 | GRCh38.p7 | 9:81628919 | CCCAGAATTCTGCAA[A/G]AGAGCACGGACCCAC | 7088 |
rs79832460 | snp | A/C | 0.299664 | 0.245017 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689784 | CGTTCTCCCTCCCCC[A/C]CTCCTCTCGCTTCCA | 7088 |
rs79921273 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TLE1 | GRCh38.p7 | 9:81620082 | TGCAGAGACCTTATT[C/T]AAAAATTGAGAACGC | 7088 |
rs79927696 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81664928 | TGGACTGGGGAACAT[G/T]CTTTGAGAAGCACTG | 7088 |
rs79928362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81642818 | GAGAGCCAAGATACC[A/G]AACAACCCAAATGTC | 7088 |
rs79932246 | snp | A/G | 0.124491 | 0.216211 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586689 | AACTTCAAGCTGAGC[A/G]ATGGGCATGTGGCAT | 7088 |
rs79955842 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81627460 | ACACCTCTACCTGGT[A/G]CAGGCTCCTGACAAT | 7088 |
rs80041317 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81653675 | AAAAGATATAAAAGA[C/T]ACCTGAATTTTCAGT | 7088 |
rs80050205 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81606786 | ATAATTAAAAAAAAA[A/C]CCATATATATATATA | 7088 |
rs80134532 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | TLE1 | GRCh38.p7 | 9:81682922 | CCTTTTCGGTAACCC[A/G]CCACAAACGGGAGCA | 7088 |
rs80171484 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | TLE1 | GRCh38.p7 | 9:81603727 | TGATACAAGGTCAGG[C/T]GTGGTGGCTCATGCC | 7088 |
rs80213103 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588015 | GAGGGGAAACAGCAC[C/G]TGCGATTGTCTTTCC | 7088 |
rs80227870 | snp | A/C | 0.136166 | 0.22258 | intron-variant | TLE1 | GRCh38.p7 | 9:81596526 | AGGGCTCATCATGAC[A/C]ATGGTGAAGGGATCC | 7088 |
rs80248099 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81662350 | ACGGTGTTAGTATTA[A/G]TGTGCCTGTTTTGTG | 7088 |
rs80265805 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81625004 | AAAGGGAGAAGCATA[C/T]CTGAGAAGTCTAAAA | 7088 |
rs80285818 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | TLE1 | GRCh38.p7 | 9:81647800 | TCCATCTGATCCCAA[C/G]GCCCATGCTTTGTCC | 7088 |
rs80293668 | snp | A/C | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81664253 | GACACTGCCTCTACC[A/C]AAAAAAAAAAAAACT | 7088 |
rs80322156 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81638395 | TAAATGAGTAGAGGG[G/T]CCAAATCTAGAAGAG | 7088 |
rs80347443 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | TLE1 | GRCh38.p7 | 9:81679225 | ATAAAATCATATATC[A/C]ACACTTCCTGGATTT | 7088 |
rs111242955 | snp | A/G/T | 0.5 | 0 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588319 | ATTCCTGTTTCCATG[A/G/T]GTGAATCAACACAGC | 7088 |
rs111283291 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TLE1 | GRCh38.p7 | 9:81592520 | CCGGGTCTTTGCAGT[A/G]ACAGCCTTTAACCCT | 7088 |
rs111327433 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679801 | ACGAAATCAATCAAA[A/G]CTTTGAGGAAAGCCA | 7088 |
rs111360748 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81632087 | AGAGCGAAGACTCCA[C/T]CTCAAAAAAAAAAAG | 7088 |
rs111372614 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81642709 | AAAAAATGAAAGAAA[A/G]GAAAGAAAGGAAAGA | 7088 |
rs111435537 | snp | A/G | 0.000115303 | 0.00759199 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593142 | GCTGATGGTCACAGC[A/G]CACACCACCTCCCCG | 7088 |
rs111451320 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81662726 | TTAGCAAAGTGGCCA[A/G]GCACCGTAAATTGAT | 7088 |
rs111465279 | in-del | -/AAC | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81637571 | CTTCTAGGTCCCCTG[-/AAC]AAACAGCTCACTGTC | 7088 |
rs111478661 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81657361 | GTAAAGATTAGAACA[C/T]ATCAATATCATAAAA | 7088 |
rs111516258 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81677246 | CGTCTTCCCCCCCCC[A/C]AAAAAAAGACCTTAC | 7088 |
rs111516638 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81590745 | GCCAGAGAGAAGCAG[A/C]GGTGATAGGCCCAGC | 7088 |
rs111524366 | snp | C/T | 0.5 | 0 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585545 | CACGCAGCTCTCATG[C/T]AGGTGCAGCTGGTAC | 7088 |
rs111556931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673229 | AGTGAACCAAGATTG[C/T]GCCATTGCACTCCAG | 7088 |
rs111574855 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | TLE1 | GRCh38.p7 | 9:81592101 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 7088 |
rs111605329 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81618536 | ACTTCAAATTACAAC[A/C]AATGAGGAAGCCTGG | 7088 |
rs111607551 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TLE1 | GRCh38.p7 | 9:81593573 | CAAATCTCATTATAA[A/G]ACACTTAATGTACTT | 7088 |
rs111635993 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81628975 | GTAGGTCTATACACC[A/G]TCTGCTCTGGAGTCT | 7088 |
rs111702055 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81626358 | ACGCACCCCATCACA[C/T]CTGTGTGCCTTCTCC | 7088 |
rs111723579 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | TLE1 | GRCh38.p7 | 9:81603813 | TCAAGACCAGCCTGG[C/T]CAACATGGTGAAACC | 7088 |
rs111731924 | in-del | -/G | 0.0486741 | 0.148216 | intron-variant | TLE1 | GRCh38.p7 | 9:81620134 | TACACCAAGGGAGGC[-/G]GGGGGGCCCGGGGGA | 7088 |
rs111734682 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TLE1 | GRCh38.p7 | 9:81641612 | CTAATTTAAAAATGG[A/G]CAAAGGACCTCCTGA | 7088 |
rs111770125 | snp | C/T | 0.5 | 0 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588811 | TCCAGTAAAGAACTG[C/T]GTGGGAATTTCAACA | 7088 |
rs111790182 | in-del | -/A | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81683425 | CCCTCTCTACAATAT[-/A]AATGAGCACTTAGGC | 7088 |
rs111812077 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81615122 | AAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAGAAG | 7088 |
rs111864142 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81592937 | TCTATTTCCTCATAA[C/T]GGGAATAAAACCCAG | 7088 |
rs111866732 | in-del | -/AGATT | 0.173643 | 0.238054 | intron-variant | TLE1 | GRCh38.p7 | 9:81663349 | CAAGATCATAGAGCA[-/AGATT]AAGAAGCCACATATT | 7088 |
rs111867781 | snp | C/T | 0.5 | 0 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585623 | GCCCACTGCCAGCCA[C/T]TCCCCGGTGGGGCAG | 7088 |
rs111871163 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687591 | CCTTCACTATGGGGA[C/G]GGGGAAAGCGGACCC | 7088 |
rs111873502 | snp | G/T | 0.000133092 | 0.00815647 | intron-variant | TLE1 | GRCh38.p7 | 9:81620589 | TTAATCAAAGATTTC[G/T]TCCCAAGCCTCTTTG | 7088 |
rs111896471 | snp | C/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81650497 | GAAAAAATTCTGTGC[C/T]TGAGCTACAAGTACA | 7088 |
rs111896866 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81655087 | GAAGGCAGGAAAGGC[C/G/T]GGGTGCGGTGGCTCG | 7088 |
rs111911478 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81594285 | GGAACCAACCCAAAT[A/G]CCCATCAATGACAGA | 7088 |
rs111921611 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595533 | CATAAAATTAAACAA[C/T]TGAGGCTGGGCGCGG | 7088 |
rs111944659 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81598239 | GACCTTAAACTCCCA[A/G]CCACACAGGACAACA | 7088 |
rs111952040 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81685014 | AACTTGCAAACTCAT[A/G]GTCATTGCTAGAGCT | 7088 |
rs111966661 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682684 | AACCACCAGGCTCAC[A/G]TCAACTTGCTGTTTT | 7088 |
rs111966895 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81599254 | ACTCGCCCATAACCA[C/T]GGCTAGTAAGCGGTA | 7088 |
rs112057426 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81591875 | TGTTTCCAAAACACC[A/G]CCACTCTGCTTTTTG | 7088 |
rs112060359 | snp | C/T | 0.444444 | 0.157135 | intron-variant | TLE1 | GRCh38.p7 | 9:81611459 | TCAAATAAAAAAAAT[C/T]GACTTTGGTGGGAGA | 7088 |
rs112079380 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81678198 | TCAAAGAAGGTAAAT[A/G]GAATACAATTTATTG | 7088 |
rs112123862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81626556 | ACTGGCAACCATATC[A/G]TATCTCAGAACCCTG | 7088 |
rs112130718 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81594497 | TGAGAACAATGAGAT[C/T]GCGCCACTGCACTCC | 7088 |
rs112133989 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81601604 | GCTACAGTGCCAGAA[A/G]AAAAAAAAAAAAGTC | 7088 |
rs112142324 | snp | C/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81637112 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCTGAGG | 7088 |
rs112143051 | in-del | -/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81641340 | CTCCCATTATGTGAA[-/T]TGGCCTCTCACGTAA | 7088 |
rs112220777 | snp | C/T | 0.333722 | 0.235565 | intron-variant | TLE1 | GRCh38.p7 | 9:81631892 | CGGATCACCTGAGGT[C/T]GGGAGTTCCAGACCA | 7088 |
rs112228768 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81624884 | ACCTGGGCAAATCAG[A/C]TGAAAACACACTGTT | 7088 |
rs112291416 | snp | A/C | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81606801 | ACCATATATATATAT[A/C]TAGAGAGAGAGGCAG | 7088 |
rs112298282 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81590081 | CTTCCCAGCAAAGAT[A/G]AAACAAGAGTAAAAC | 7088 |
rs112325064 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81611644 | GGGCGTCTTTGTCTC[C/T]GAGGTGTGTGGGGCT | 7088 |
rs112335058 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | TLE1 | GRCh38.p7 | 9:81592097 | GGCGCGGTGGCTCAC[A/G]CCTATAATCCCAGCA | 7088 |
rs112338904 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | TLE1 | GRCh38.p7 | 9:81675940 | TCCTGACCTCGTGAT[C/T]CGCCCGCCTCAGCCT | 7088 |
rs112353207 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629165 | GCTCAACAAATATTT[C/G]TCAAATGACTCAAAG | 7088 |
rs112371922 | in-del | -/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81662309 | TGCTAAAATGACCAA[-/G]ACATTCACTAGATGA | 7088 |
rs112382826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587615 | TAAAGGAGGGAGGGT[G/T]GTGAGGAGGAAGACA | 7088 |
rs112431086 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81636242 | TAATTCTTGCTCTGT[C/T]ACCTTTTAAGAGCTT | 7088 |
rs112484984 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | TLE1 | GRCh38.p7 | 9:81610092 | AAGTGTTAACACTCC[A/T]CAGGAAAAGACACCA | 7088 |
rs112501764 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81617066 | TTGAGATCTGCACAC[C/T]CTTATATCAGAGTTT | 7088 |
rs112506321 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | TLE1 | GRCh38.p7 | 9:81592119 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCGGGCG | 7088 |
rs112521268 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81585255 | TTGTCGTCTCCCAAC[C/G]CCTCCAAAACAAACT | 7088 |
rs112523583 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81622642 | CTTGAGCGGCTTAAA[C/T]GAAGCTTATAATCTG | 7088 |
rs112560737 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81591867 | AAAGTCTGTGTTTCC[A/G]AAACACCGCCACTCT | 7088 |
rs112565529 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81632430 | TTTTATCTTCCCCCC[A/C]AAACTTATACCAAAA | 7088 |
rs112579393 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81591765 | TGCTATAGAATATTG[A/G]GCCATATTTAAATAA | 7088 |
rs112583578 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81591383 | CTACCTCATCACCCT[A/G]CATTATTTACCACTT | 7088 |
rs112584752 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81601072 | ATATCCATATCTATA[G/T]TTTATTGGTTCTGTT | 7088 |
rs112639712 | in-del | -/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81683223 | TTCCCCATCACTGCA[-/T]TTTTTTTTTTTTTTT | 7088 |
rs112650769 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81597029 | CAAATCAAGTGCCCA[A/G]ACTTTGCTGTTAAAT | 7088 |
rs112716185 | in-del | -/A/AAAA | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81666804 | AATAAATAAATAAAT[-/A/AAAA]AAATAAAATAAAATA | 7088 |
rs112744044 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583500 | TAGTCTTGAGCTCCC[A/G]GTAACTCAAGCTTGT | 7088 |
rs112768572 | snp | C/G | 0.000386428 | 0.0138948 | intron-variant | TLE1 | GRCh38.p7 | 9:81585674 | CAAGGAGCAAGACAG[C/G]CTCACTCATTATTCC | 7088 |
rs112773031 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81631237 | ATAACCCTCCCTCCA[A/C]CCACTCCAATGAACC | 7088 |
rs112773867 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TLE1 | GRCh38.p7 | 9:81621249 | AGGATACTTTCATTC[A/G]CATATGCCGAGTAGG | 7088 |
rs112851600 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81623350 | ACCTGGGTATTGACT[A/G]AATTGTCATTTTGAT | 7088 |
rs112861924 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588620 | CAGCCAACAGGGATC[C/T]GCTGAGCACAGATGC | 7088 |
rs112862287 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663784 | GGCACCTGCCACCAC[A/G]CCCGGCTAATTTTTG | 7088 |
rs112866225 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690304 | CTGAGGTTTGTTTTT[C/T]CTTGAGCTGCCTTTT | 7088 |
rs112877801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81660445 | TTGAGACAGAGTCTC[A/G]TTCTGTCGCCCAAGC | 7088 |
rs112915287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585970 | GAAATACGATCATAT[A/G]TCACCTATCAAGGGG | 7088 |
rs112934485 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TLE1 | GRCh38.p7 | 9:81615423 | ATCCCCCAAGTAAGA[C/T]GGCAATGAGGCTGGG | 7088 |
rs112965739 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | TLE1 | GRCh38.p7 | 9:81627958 | GTGCGGTGGCTCACG[C/T]CTGTAATCTCAGCAC | 7088 |
rs113025240 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81621454 | ACTGCCCTGAACAAT[-/G]TTGAATGAGCTGTGC | 7088 |
rs113029067 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81594663 | TGAAGTATGCACTGC[C/T]TCCTCCTTCCCATTA | 7088 |
rs113041040 | snp | C/G/T | 0.0511248 | 0.152339 | intron-variant | TLE1 | GRCh38.p7 | 9:81621846 | CCAAGCCTCTTGGCC[C/G/T]GCCTCAGGGACTGAC | 7088 |
rs113043151 | snp | A/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81608839 | CTACTCGAGAGGCTG[A/T]GACAGAAGAATTGCT | 7088 |
rs113044458 | snp | A/G | 0.225893 | 0.248835 | intron-variant | TLE1 | GRCh38.p7 | 9:81613961 | CACCCAAGCTGGAGT[A/G]CAGTGGCGCAATCTC | 7088 |
rs113045352 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | TLE1 | GRCh38.p7 | 9:81659303 | CTTCCACCTCTTGCA[A/C]AGGCTAGACAACTCC | 7088 |
rs113125910 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663636 | ACTTTTTTTTTTTTT[C/T]TTTTGAGATGGAGTC | 7088 |
rs113162555 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81604036 | ACAAAAAAAGGTGAT[A/G]CAAGCTGTCTGCTCT | 7088 |
rs113165560 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81585264 | CCCAACCCCTCCAAA[A/G]CAAACTTGTGTCCAA | 7088 |
rs113174660 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81616779 | TTTCTTTCTATAGTT[C/T]CTGGTAGCAGACAGA | 7088 |
rs113195839 | snp | C/T | 0.444444 | 0.157135 | intron-variant | TLE1 | GRCh38.p7 | 9:81610545 | ACTGAGAACCACTTC[C/T]CCATGGTAAATACTT | 7088 |
rs113216436 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670727 | CAGAAAAAAAAAAAT[A/T]AAAAAAAAAAAATCA | 7088 |
rs113253629 | snp | C/T | 0.318174 | 0.240525 | intron-variant | TLE1 | GRCh38.p7 | 9:81631884 | GAGGCAGGCGGATCA[C/T]CTGAGGTTGGGAGTT | 7088 |
rs113264158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81673951 | TCCTTTATTCTCTCC[A/G]TACCAGACCAAGACG | 7088 |
rs113273526 | in-del | -/GTGTGTGTGTGT | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81633289 | TGTCAGAAGGGGACC[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 7088 |
rs113282087 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | TLE1 | GRCh38.p7 | 9:81616322 | CTGCAAACATGCCAT[A/T]AAAAAAAAACCCCGC | 7088 |
rs113310260 | snp | A/C/T | 4.94257e-05 | 0.004971 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81584291 | ACAGCTAAGCACTGA[A/C/T]GAGGACTCTTTGGAC | 7088 |
rs113315509 | snp | C/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81617794 | ACTTTGGGAGGCCGA[C/G]GCAGGTGGATCACGA | 7088 |
rs113349275 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | TLE1 | GRCh38.p7 | 9:81624253 | AAAATAGAAACGTGT[A/G]ATTTTTAAATGAACA | 7088 |
rs113359646 | in-del | -/G | 0 | 0 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689784 | GTTCTCCCTCCCCCC[-/G]CTCCTCTCGCTTCCA | 7088 |
rs113370243 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585962 | CACTAACTGAAATAC[A/G]ATCATATATCACCTA | 7088 |
rs113393744 | in-del | -/G/GGAAAGAAC | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81642726 | AAGAAAGGAAAGAAA[-/G/GGAAAGAAC]GAAAGAAAGAGAGAG | 7088 |
rs113413898 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81634723 | TAAGATGCCACAGAT[C/T]TTCAGACTCACGCTG | 7088 |
rs113439505 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632475 | AAATGTTCAGTATCC[C/T]TTTTTTTTTTTTTTT | 7088 |
rs113471832 | snp | A/G | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81675935 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 7088 |
rs113493594 | in-del | -/TCTC | 0.0138799 | 0.0821421 | intron-variant | TLE1 | GRCh38.p7 | 9:81632584 | GAAAAGGGGCTGAAT[-/TCTC]TCTATTTGCTACACA | 7088 |
rs113526966 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81660879 | AGGCGGGAGGATCAC[A/G]AGGTCAGGAGGTCAA | 7088 |
rs113529268 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81612607 | CTAGCAGAAAACCAG[A/C]AAACTATAGTCTGCA | 7088 |
rs113580039 | snp | A/C | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81585251 | CTCATTGTCGTCTCC[A/C]AACCCCTCCAAAACA | 7088 |
rs113585918 | snp | G/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81604826 | GACTGTGCCTCCCCG[G/T]TTCCATGGGAAACTC | 7088 |
rs113621176 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81618042 | AAACAACAACAACAA[A/C]AAAAAATTCAATGAT | 7088 |
rs113623016 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81666247 | AACTCCGCAGAGTGA[A/G]TCACAGATCATCACC | 7088 |
rs113654188 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686353 | GCTGGTCCCTTTCAA[A/C]ACCTTTGGTTTTTAA | 7088 |
rs113692869 | in-del | -/CCT | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81628789 | ACCGGATGCACCCAG[-/CCT]CCTTGATAAAACCAT | 7088 |
rs113699107 | snp | C/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81591684 | CTTACATGCTTTTAA[C/T]GATGGATTATCTTTC | 7088 |
rs113706945 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81615628 | AGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 7088 |
rs113709993 | snp | A/G | 0.1652 | 0.235179 | intron-variant | TLE1 | GRCh38.p7 | 9:81617808 | AGGCAGGTGGATCAC[A/G]AGGTCAGGAGCTCGA | 7088 |
rs113739695 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TLE1 | GRCh38.p7 | 9:81659706 | AGCCCTCATCATCCA[A/G]AAATTAGGGTTTGCA | 7088 |
rs113783637 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687794 | ACCCCGGGGACCAGA[A/G]GAGAAAAACAACTCC | 7088 |
rs113828813 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | TLE1 | GRCh38.p7 | 9:81607024 | AGCCCAGGAGTTTGA[A/T]ACCAGCCTAGGCAAC | 7088 |
rs113848868 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587121 | ATTTATACATTATTT[C/G]AAAAGTCTGCAAATC | 7088 |
rs113858141 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81609282 | TAGAGACGGGGTTTC[A/G]CCACATTGGCCAGGC | 7088 |
rs113880365 | snp | A/T | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81601783 | ACCTCTTATAAACCA[A/T]CACTACTTAATAATT | 7088 |
rs113917070 | in-del | -/CCAT/CCATCCAT | 0.5 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81584965 | TAGGCACTCATCCAC[-/CCAT/CCATCCAT]CCATCCATCCATCCA | 7088 |
rs113940353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589541 | CCGGCACGGAGCAAG[A/G]GTTCAGAGTACAGAC | 7088 |
rs113951327 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81677497 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 7088 |
rs113954130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684709 | TGTTGCACTTTGAAA[C/T]GTGTCCAACTGTGCA | 7088 |
rs114026374 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81661792 | ACACAGAAACCTCAC[C/T]GGCAACCAAACAAAA | 7088 |
rs114031378 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81614332 | CAATATGCCTAAAAA[C/G]AACAACACTTTGGAG | 7088 |
rs114044562 | snp | G/T | 0.0520825 | 0.152737 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688510 | CTGCGCGGAGACGTC[G/T]GGCGCTCGGGGACTG | 7088 |
rs114062202 | snp | C/T | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587224 | TTGAGCTCTCTGGTG[C/T]GGGGTAAATAAATGA | 7088 |
rs114065597 | snp | C/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690020 | ACGTGGGGCTGGCTA[C/G]AGAGCGCGCGGGCGC | 7088 |
rs114105775 | snp | C/G | 0.0119091 | 0.0762411 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690039 | GCGCGCGGGCGCGCG[C/G]TAGCGGGAGGGACTG | 7088 |
rs114157429 | snp | A/G | 0.029116 | 0.117091 | intron-variant | TLE1 | GRCh38.p7 | 9:81597058 | ATGAACCTCTCTCTG[A/G]TTCTCTGGCTACGTC | 7088 |
rs114163697 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81659512 | AAATCTGCATGAAAC[A/C]CTCCACTCAGAAATG | 7088 |
rs114220627 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | TLE1 | GRCh38.p7 | 9:81596318 | CCATATGGATGTTAA[C/T]ACATCAGTCACAGGG | 7088 |
rs114222506 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TLE1 | GRCh38.p7 | 9:81674700 | GACTTTGTAAGGGGA[A/G]TCCAGCTTTTCTGCG | 7088 |
rs114270209 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686947 | CTAGTATGGCAAACA[A/G]CGATTTCAACATGGC | 7088 |
rs114350325 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | TLE1 | GRCh38.p7 | 9:81622288 | TTCAACTTTAAATCC[A/G]CCCAAGTGCCCAGCA | 7088 |
rs114400198 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TLE1 | GRCh38.p7 | 9:81652931 | CTTTTATAGCCTTTT[A/G]ATTCTTTACCCTCCA | 7088 |
rs114400644 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81651121 | TTAATCCGTACAGCA[G/T]CATGTCTAATTATCA | 7088 |
rs114432866 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588590 | CTTCATTCAAAAATC[A/G]CCATCAGAAACGATC | 7088 |
rs114472986 | snp | C/T | 0.031825 | 0.122064 | intron-variant | TLE1 | GRCh38.p7 | 9:81652446 | TTCACAGAACATAGA[C/T]AGGGAAAGAAAAACT | 7088 |
rs114491850 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81639344 | GTGCTAGATTACAAG[C/T]GTAAGCTACCATAGC | 7088 |
rs114494164 | snp | A/T | 0.0640965 | 0.167152 | intron-variant | TLE1 | GRCh38.p7 | 9:81680017 | TCTTTCTGTTTCTTA[A/T]TAAACACTATTTGGG | 7088 |
rs114502158 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81679009 | AAAAATTAACCAGGC[A/G]TGGTGATGCACGCCT | 7088 |
rs114524516 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | TLE1 | GRCh38.p7 | 9:81678197 | TTCAAAGAAGGTAAA[C/T]AGAATACAATTTATT | 7088 |
rs114529653 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | TLE1 | GRCh38.p7 | 9:81638667 | GTCTTCACTGTTGCC[C/G]AGGCTGGAATACAGT | 7088 |
rs114565638 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | TLE1 | GRCh38.p7 | 9:81592394 | TCCGAACATGTCCCA[A/G]CATGTTTTATGTCCC | 7088 |
rs114598655 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | TLE1 | GRCh38.p7 | 9:81625663 | GAGAGCACCCAGTGG[C/T]GTCAAAAGAAAATGT | 7088 |
rs114609486 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81683034 | CACAATTATACCATT[C/T]TTGATTTGGATGCAC | 7088 |
rs114633202 | snp | A/G | 0.00156431 | 0.0279233 | synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81652262 | CTGTTTGGCACGTTC[A/G]ACAGCCTGGGCCACC | 7088 |
rs114637637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81609663 | TGCTTTTTATAATTC[C/T]AGATCTCTTGGAGCA | 7088 |
rs114696997 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590247 | ACTGCAGCTGCTGCT[A/T]AGGTGACAGGGCTGA | 7088 |
rs114713404 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81646482 | AGGATATGCATTATT[C/G]TCCTAGGGAGAATTT | 7088 |
rs114721524 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | TLE1 | GRCh38.p7 | 9:81602784 | AGCTAGGACCTTACT[C/G]ACAAAACTGGGCATG | 7088 |
rs114809856 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687895 | GTAAATAGGCGAGAG[A/G]AGAAACAAAGGGGGG | 7088 |
rs114828695 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TLE1 | GRCh38.p7 | 9:81646097 | ACAAACCTGCACATC[C/T]TATACATGTATCCCG | 7088 |
rs114847675 | snp | A/G | 0.271162 | 0.249103 | intron-variant | TLE1 | GRCh38.p7 | 9:81655865 | CTCAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 7088 |
rs114862116 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | TLE1 | GRCh38.p7 | 9:81624144 | CTGCACTTAACATTC[G/T]AATGTGACATAATAC | 7088 |
rs114915120 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | TLE1 | GRCh38.p7 | 9:81620875 | GTGTTTTTATTCTTT[C/T]CCACTGCGACTTCCT | 7088 |
rs114958446 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | TLE1 | GRCh38.p7 | 9:81657270 | CCTTGCTTAATATGA[A/T]TTTTTTGCTGTATAG | 7088 |
rs115021573 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TLE1 | GRCh38.p7 | 9:81671292 | GCTGAAGCGGGCGGA[C/T]TGCTTGAGCCCTGGA | 7088 |
rs115075540 | snp | A/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690733 | CAAAGAGAGACAATG[A/T]AATAAACCAGCACTG | 7088 |
rs115138243 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | TLE1 | GRCh38.p7 | 9:81637412 | TCTTACTGTGAAGAG[C/G]TGATGGCTTACATAA | 7088 |
rs115190474 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81659756 | GGGGTTCTATGTTAA[A/G]TCACTTAAACCACTG | 7088 |
rs115198232 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TLE1 | GRCh38.p7 | 9:81590712 | TTCAAGAGGCTCTTA[C/T]TGTGTGGGCTGCAGG | 7088 |
rs115228506 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81660777 | ATCAGCAATCAATCA[A/G]ACTCTAGTGTATTCT | 7088 |
rs115266971 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81625761 | CAAACACCTATTCAA[A/G]ACCAAGGTAGCAAAG | 7088 |
rs115328711 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TLE1 | GRCh38.p7 | 9:81596967 | ATTCAAGAGGAAGTC[A/G]AGGGGAAGGCTCGTA | 7088 |
rs115397116 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81665380 | AGATAATAACTTTTA[C/T]GTTCCATCTCCTCAC | 7088 |
rs115434739 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81637278 | TGGGAGAATCGCTTG[A/G]ACTTGGAAAGCAGAG | 7088 |
rs115449400 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588063 | AGTGCTAAAGAAATG[A/G]AATGCCACTGCAGGT | 7088 |
rs115504888 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TLE1 | GRCh38.p7 | 9:81655059 | TAGTGTCTATAGCAC[A/G]GGCTGTTTTAAAGAA | 7088 |
rs115595956 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81628800 | CCAGCCTCCTTGATA[A/T]AACCATGGTGCTGTG | 7088 |
rs115650017 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81611681 | TCCTGCCCACGCAGC[A/G]CAGAGAGGCCTGGCC | 7088 |
rs115651880 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TLE1 | GRCh38.p7 | 9:81648510 | ATCAACTGAAAAAAA[C/T]AAATATATGTGTGTA | 7088 |
rs115728682 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | TLE1 | GRCh38.p7 | 9:81632532 | AATACTGCTATGTTC[A/G]GAAAGAAGGAGGCAA | 7088 |
rs115730846 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TLE1 | GRCh38.p7 | 9:81663609 | CCTAGCAGAGGTATC[C/T]GCACAGAATAGACTT | 7088 |
rs115749318 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | TLE1 | GRCh38.p7 | 9:81662461 | ACACTTTGCGGGGGC[C/T]GAGGTGGGTGGATCA | 7088 |
rs115757298 | snp | A/G | 0.0422008 | 0.138995 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688352 | AAGCAGAAGCGGGGA[A/G]CGCGCTGGCCACGCA | 7088 |
rs115830057 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81634998 | TCAGTACTGTGAGGA[A/G]GTATTGCAATTCCCA | 7088 |
rs115935144 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | TLE1 | GRCh38.p7 | 9:81646555 | AGGGATTAACCACAT[A/G]CTCATAAGAATAAGA | 7088 |
rs115938488 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | TLE1 | GRCh38.p7 | 9:81608171 | CCAAGCACTTTGGGA[A/G]GCCAAGGCAGGAGGA | 7088 |
rs115939653 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588466 | CCGGCCTCCTGACCT[C/G]AGAGGCATTGGGCAG | 7088 |
rs115946736 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81682836 | AGGGATCTATAAAGG[A/G]CTCCAAGAAAAAAAT | 7088 |
rs115969062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81638383 | AACATATTTATTTAA[A/G]TGAGTAGAGGGTCCA | 7088 |
rs116016721 | snp | G/T | 0.0115144 | 0.0749975 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583958 | TCCGTTCCTCAATCC[G/T]ACAACCCATGGCCCC | 7088 |
rs116045871 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686054 | CCTTGCATTTAATAG[A/G]GAAAAGGAATAATGT | 7088 |
rs116057761 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | TLE1 | GRCh38.p7 | 9:81660373 | AATCATACGTTGGTA[A/T]GTATAAAATTCATGT | 7088 |
rs116059891 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | TLE1 | GRCh38.p7 | 9:81680583 | GGACAAAAACCAGCC[A/T]CTGGCCCACTGCTGA | 7088 |
rs116121939 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687262 | CTAAGTACAGGCGCC[A/G]CCGCCACCCGGCTGG | 7088 |
rs116182669 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81653488 | AAATAGCTTATACAT[A/G]CATATGACTCATTAA | 7088 |
rs116252163 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81655008 | GACCTCACCGACAGG[G/T]CCCAGGGGTCAGCTG | 7088 |
rs116253325 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81617032 | ACAGCTGAATTTCTC[A/C/G]AGGGATGAAATCTTT | 7088 |
rs116326735 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81604627 | ATCCTTGGACACGCA[C/T]GGTCAGAGGCACACT | 7088 |
rs116347734 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | TLE1 | GRCh38.p7 | 9:81658137 | GGCTGATTTTAAACT[A/C]CTGACCTCAAGTGAT | 7088 |
rs116381546 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | TLE1 | GRCh38.p7 | 9:81593388 | AAGGAAAGATTCTCT[A/T]GTATAGTTTCCTTTG | 7088 |
rs116399162 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | TLE1 | GRCh38.p7 | 9:81616450 | CTAGAGAAATATCTT[C/T]TTTTAAAGGAAATAA | 7088 |
rs116409155 | snp | C/T | 0.00633093 | 0.0559052 | intron-variant | TLE1 | GRCh38.p7 | 9:81611731 | ATGGAGCATGCAGCG[C/T]TCCTACCCCAACCAC | 7088 |
rs116451733 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81674748 | TGACAGTTGAGAAAG[A/T]AATCACCTAAAAACC | 7088 |
rs116471884 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TLE1 | GRCh38.p7 | 9:81595427 | AAGTCCAGTAGCCAA[A/G]TTCTATGACTCAGAA | 7088 |
rs116542906 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81604008 | CTTTGTCTCAAAAAA[A/G]CAAAACAGAACAACA | 7088 |
rs116582731 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81619440 | TTAAATGAAATAATC[C/T]ATGAAAAAATCACAA | 7088 |
rs116599924 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | TLE1 | GRCh38.p7 | 9:81637755 | TAGGAAATGTGGCCA[A/T]TCCACCTCATATTCG | 7088 |
rs116601109 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81631669 | AGAAAACATGTTAAA[C/T]TGAAGTCCCAAAGCT | 7088 |
rs116638238 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TLE1 | GRCh38.p7 | 9:81646111 | CCTATACATGTATCC[C/T]GGAACTTAAATTAAA | 7088 |
rs116651736 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81630730 | CCAAGTAAAATTAGA[C/T]TTTCTAATTCAAACC | 7088 |
rs116657110 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81653581 | GATACATAAGTACAA[A/T]AGAACTATCTGCCTC | 7088 |
rs116675276 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TLE1 | GRCh38.p7 | 9:81678755 | ACATACCTGTAATCC[C/T]GGCTACTCAGGGAGG | 7088 |
rs116691289 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | TLE1 | GRCh38.p7 | 9:81634856 | TTGACTTACCACAGT[A/G]GTATGATGAGACAAA | 7088 |
rs116711411 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | TLE1 | GRCh38.p7 | 9:81647444 | TTCCTTATTAAAAGT[C/T]ATTCATGCACAACAA | 7088 |
rs116712404 | snp | G/T | 0.0119091 | 0.0762411 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690295 | AAAATTTATCTGAGG[G/T]TTGTTTTTCCTTGAG | 7088 |
rs116743404 | snp | C/G | 0.029116 | 0.117091 | intron-variant | TLE1 | GRCh38.p7 | 9:81627486 | ACAATCTAGAAACCA[C/G]TGGGGCTTTCCTTTG | 7088 |
rs116744195 | snp | A/C | 0.0821764 | 0.185298 | intron-variant | TLE1 | GRCh38.p7 | 9:81659822 | ACCAATCTACTTGAG[A/C]GTTTCATCAAAATCG | 7088 |
rs116765989 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | TLE1 | GRCh38.p7 | 9:81682351 | TGAGCAAGTCCCAGA[C/G]TCTGAACACGTGCAC | 7088 |
rs116767128 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TLE1 | GRCh38.p7 | 9:81674659 | ATAAGTCAAGTTTCA[C/T]TGAGGGGTCAGAACA | 7088 |
rs116869790 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | TLE1 | GRCh38.p7 | 9:81656493 | GCACACAGATACATA[C/T]ACAGAAATATAAAAG | 7088 |
rs116907724 | snp | A/G | 0.126909 | 0.217598 | intron-variant | TLE1 | GRCh38.p7 | 9:81595545 | CAATTGAGGCTGGGC[A/G]CGGTGGCTCACGCCT | 7088 |
rs116921346 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | TLE1 | GRCh38.p7 | 9:81599898 | GGCATACACTCTATT[G/T]TCATTTATTTTTTTT | 7088 |
rs116923155 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690731 | AACAAAGAGAGACAA[G/T]GTAATAAACCAGCAC | 7088 |
rs116996148 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | TLE1 | GRCh38.p7 | 9:81668113 | GAGGTCGCGATGAGC[C/T]GAGATCGCGCCACTG | 7088 |
rs117018389 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | TLE1 | GRCh38.p7 | 9:81659437 | TTCCCTGTGCCTAGA[A/T]TTTTTAATACTGTGT | 7088 |
rs117118923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656128 | CTTGCTTTAGCCAGC[A/G]AGGCAGATATATGCA | 7088 |
rs117139705 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81602265 | GCACCGGAAAAGCAG[C/G]CTGGGGGGATATTAC | 7088 |
rs117167900 | snp | C/G | 0.0652144 | 0.168387 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688335 | AATTAAGCCGGAAAG[C/G]CAAGCAGAAGCGGGG | 7088 |
rs117349786 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | TLE1 | GRCh38.p7 | 9:81649560 | GATCTTTCACACTTG[G/T]AATAGATGTCTAAAC | 7088 |
rs117353257 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | TLE1 | GRCh38.p7 | 9:81643871 | TTCAGCTAATCCACA[C/T]AGGCCAACTCCTCCT | 7088 |
rs117363404 | snp | C/T | 0.0162398 | 0.0886349 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690958 | TTTGGTTTTTGTGTA[C/T]GTCTCTAAATACACA | 7088 |
rs117428137 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | TLE1 | GRCh38.p7 | 9:81648555 | TCTATATTATCCCTC[C/G]ATTATCTGTGATGTA | 7088 |
rs117485564 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | TLE1 | GRCh38.p7 | 9:81656149 | GATATATGCAAAAAG[A/G]GTGCAGCTGTACCAG | 7088 |
rs117506369 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TLE1 | GRCh38.p7 | 9:81619921 | CTAGAATGCTCACTA[C/T]GGAAGACATTGAGCT | 7088 |
rs117602479 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81644648 | TTTTATAGTCGTGAT[C/G]GTTGTACAGCAATGT | 7088 |
rs117611981 | snp | A/T | 0.159688 | 0.233117 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587955 | GTGTGTGATCCCGCC[A/T]GTGTCTGCTGATGTG | 7088 |
rs117671510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673646 | CACTCACCTGTTTTC[A/T]CTTTTTCAAGGTGGA | 7088 |
rs117718331 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TLE1 | GRCh38.p7 | 9:81592542 | TTTAACCCTTTCCTG[A/G]AGTTAAGGCCATAAA | 7088 |
rs117721109 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81684039 | CCCTTGTAAAAGAGT[C/T]AATGAGGTTATTAAA | 7088 |
rs117734305 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81636495 | ACAAGCAAGTGCAGC[A/G]GGTAATTAAGCACGG | 7088 |
rs117743982 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | TLE1 | GRCh38.p7 | 9:81659385 | CCCAATGATGAATAC[C/G]TATTTGGTACCCACT | 7088 |
rs117751648 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | TLE1 | GRCh38.p7 | 9:81640682 | AGAATTTTAATTCAC[A/G]TTTTACTTAGTGCAG | 7088 |
rs117833782 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | TLE1 | GRCh38.p7 | 9:81654960 | ATCCTGAGTATTCGG[A/G]AAGTTTCGCCACAGT | 7088 |
rs117872386 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81604721 | TTAAGGTCCCTCCTG[C/T]CCCAACTGAACTCTT | 7088 |
rs117892550 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TLE1 | GRCh38.p7 | 9:81684200 | TTTATTTGCATAATT[C/T]ACTTAAATGACGATA | 7088 |
rs117936182 | snp | A/C/G | 0.00279242 | 0.0372774 | intron-variant | TLE1 | GRCh38.p7 | 9:81623445 | AGGACACCATTTGCA[A/C/G]AAGAATGAAACAGAG | 7088 |
rs117967309 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TLE1 | GRCh38.p7 | 9:81621442 | CAGTGATGTGTTACT[A/G]CCCTGAACAATGTTG | 7088 |
rs117985698 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | TLE1 | GRCh38.p7 | 9:81640631 | CCCACAAGGAATAAA[A/G]CGATCTCATCCATGT | 7088 |
rs117996056 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | TLE1 | GRCh38.p7 | 9:81599469 | GGGGCTGGGGGAACC[A/G]GGCTCCTTATGGAAT | 7088 |