SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11150 | snp | C/T | 0.295529 | 0.245828 | utr-variant-3-prime, synonymous-codon | TLE2 | GRCh38.p7 | 19:2997899 | AAATAACAAATACAT[C/T]GTGACAGGCTCGGGG | 7089 |
rs14089 | snp | A/G | 0.272921 | 0.248947 | utr-variant-3-prime | TLE2 | GRCh38.p7 | 19:2997792 | GGGGAATCAGCAGCC[A/G]GGACAGACATCCTAG | 7089 |
rs83488 | snp | A/G | 0.214239 | 0.247429 | intron-variant | TLE2 | GRCh38.p7 | 19:3006276 | GCGGAGCTCGTAGTC[A/G]CATGGGACAAGGCTT | 7089 |
rs188621 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TLE2 | GRCh38.p7 | 19:3017514 | gaagggagctgtgat[C/T]gtgccactgcactcc | 7089 |
rs216267 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TLE2 | GRCh38.p7 | 19:3012450 | tccaactcctgttct[C/T]gagtgatcgtcctgc | 7089 |
rs216268 | snp | A/G | 0.108402 | 0.206034 | intron-variant | TLE2 | GRCh38.p7 | 19:3012559 | ATTAGAAACTCCGGG[A/G]TGGGCTCGTGGAGAG | 7089 |
rs216269 | snp | A/G | 0.093777 | 0.195178 | intron-variant | TLE2 | GRCh38.p7 | 19:3012885 | ACCCGCGAGAGAGTG[A/G]ATGGGACGACTGTGG | 7089 |
rs216270 | snp | A/G | 0.493477 | 0.0567349 | intron-variant | TLE2 | GRCh38.p7 | 19:3013229 | CAGGAGGTCCAACTG[A/G]AAACTTGTTCCTATA | 7089 |
rs216271 | snp | A/G | 0.499996 | 0.00139776 | intron-variant | TLE2 | GRCh38.p7 | 19:3013618 | GTAGCGTCTGCTTCG[A/G]GGCCCCCGGGATGAA | 7089 |
rs216272 | snp | A/T | 0.424503 | 0.179021 | intron-variant | TLE2 | GRCh38.p7 | 19:3013973 | GCTGCCTCAGTTTAC[A/T]CATCTGTAAAATGTA | 7089 |
rs216273 | snp | A/G | 0.399983 | 0.200013 | intron-variant | TLE2 | GRCh38.p7 | 19:3014641 | TGGGGGAGAGAGCTC[A/G]TTGTGGTCATGCCCC | 7089 |
rs216274 | snp | A/G | 0.116138 | 0.211142 | intron-variant | TLE2 | GRCh38.p7 | 19:3003987 | gctgagattacaggc[A/G]tgagccactgcaccc | 7089 |
rs216275 | snp | C/G | 0.227959 | 0.249026 | intron-variant | TLE2 | GRCh38.p7 | 19:3004643 | aaaaaaGAGGAGCTT[C/G]GGAGTTAGGAGTTAG | 7089 |
rs216276 | snp | A/G | 0.311859 | 0.242226 | intron-variant | TLE2 | GRCh38.p7 | 19:3004794 | CCTCAGAGCTGTCCC[A/G]GAGTATGGTGTGCAT | 7089 |
rs216277 | snp | C/G | 0.321053 | 0.23969 | intron-variant | TLE2 | GRCh38.p7 | 19:3004843 | CCCTGAATGACAGAA[C/G]AAGGAGCTCACAGCT | 7089 |
rs216278 | snp | C/G | 0.222928 | 0.24853 | intron-variant | TLE2 | GRCh38.p7 | 19:3005110 | CGCTCTCGGCGGCGT[C/G]CAGAGATTAAAGGCT | 7089 |
rs216279 | snp | C/G | 0.128976 | 0.218754 | intron-variant | TLE2 | GRCh38.p7 | 19:3005233 | CCCACAGCTTCCTAT[C/G]AATCAGCTCTTTTGT | 7089 |
rs216280 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | TLE2 | GRCh38.p7 | 19:3006946 | cgccaccatgcctgg[A/C]taagttttttgtatt | 7089 |
rs216281 | snp | C/T | 0.443195 | 0.158668 | intron-variant | TLE2 | GRCh38.p7 | 19:3007321 | tctcaaactcctgac[C/T]tcaaatgatcctccc | 7089 |
rs216282 | snp | A/G | 0.214541 | 0.247473 | intron-variant | TLE2 | GRCh38.p7 | 19:3007370 | gctgggattacaggc[A/G]tgagccaccgggccc | 7089 |
rs216283 | snp | G/T | 0.442926 | 0.158996 | intron-variant | TLE2 | GRCh38.p7 | 19:3007700 | TGGAACACTCAAGGT[G/T]TCTTTGTGGGTCCTC | 7089 |
rs216284 | snp | A/G | 0.279461 | 0.248258 | intron-variant | TLE2 | GRCh38.p7 | 19:3009790 | GCACATGGAAACTCT[A/G]AATGAAAGGCCAGGG | 7089 |
rs216285 | snp | A/G | 0.442791 | 0.15916 | intron-variant | TLE2 | GRCh38.p7 | 19:3009887 | aacaaaagaaaaaaa[A/G]agagagagaaaGTCG | 7089 |
rs306029 | snp | C/T | 0.0100644 | 0.0702206 | intron-variant | TLE2 | GRCh38.p7 | 19:3019516 | TCTTGGGCTGGGGAC[C/T]GCTGGGCTCCTGCCG | 7089 |
rs306030 | snp | C/T | 0.145305 | 0.227022 | intron-variant | TLE2 | GRCh38.p7 | 19:3017961 | GTGGGGTGGTGGGGG[C/T]GGGGGGCTTTATAAA | 7089 |
rs306031 | snp | A/G | 0.142609 | 0.225759 | intron-variant | TLE2 | GRCh38.p7 | 19:3017317 | aaccctgtctctact[A/G]aaaattcaaaaatta | 7089 |
rs306044 | snp | C/T | 0.491421 | 0.0649309 | intron-variant | TLE2 | GRCh38.p7 | 19:3043407 | ggcggatcacgaggt[C/T]aggcgttcgagacca | 7089 |
rs306045 | snp | A/G | 0.128288 | 0.218372 | intron-variant | TLE2 | GRCh38.p7 | 19:3041702 | ggacccagacggagc[A/G]cctctcgaccctcgt | 7089 |
rs306046 | snp | A/C | 0.499187 | 0.0201513 | intron-variant | TLE2 | GRCh38.p7 | 19:3041265 | ctgaggcaggtggat[A/C]atttgaggtcaagag | 7089 |
rs306047 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | TLE2 | GRCh38.p7 | 19:3040186 | AGAGACGGGAGTCCA[C/T]GGCGATCCTAGGAGG | 7089 |
rs306048 | snp | G/T | 0.499767 | 0.0107802 | intron-variant | TLE2 | GRCh38.p7 | 19:3040156 | GGTGAACCCCCAACT[G/T]GGTACAGAGGGGTTA | 7089 |
rs306049 | snp | C/G | 0.327492 | 0.251694 | intron-variant | TLE2 | GRCh38.p7 | 19:3039492 | gaaaggaagagaaag[C/G]ctggccgtggttcag | 7089 |
rs373172 | snp | A/G | 0.178144 | 0.239451 | intron-variant | TLE2 | GRCh38.p7 | 19:3002899 | AGACGGCGTTTCACC[A/G]TATTGGCCAGGCTGG | 7089 |
rs375069 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | TLE2 | GRCh38.p7 | 19:2999034 | GGCACGGTGGctcgg[C/T]gcttccggaggccga | 7089 |
rs375083 | snp | C/G | 0.487113 | 0.0792303 | intron-variant | TLE2 | GRCh38.p7 | 19:2999040 | GTGGctcggcgcttc[C/G]ggaggccgaggcagg | 7089 |
rs416799 | snp | A/G | 0.165248 | 0.235196 | intron-variant | TLE2 | GRCh38.p7 | 19:2997978 | GGGAAGGGAGAGAGA[A/G]AAGGGCACAGTGAGG | 7089 |
rs513955 | snp | A/G | 0.480853 | 0.0959518 | intron-variant | TLE2 | GRCh38.p7 | 19:3000289 | accatattagccagg[A/G]tggtctcgatctcct | 7089 |
rs518399 | snp | C/T | 0.472896 | 0.113214 | intron-variant | TLE2 | GRCh38.p7 | 19:3000374 | gcgaccgtgcccggc[C/T]GGCaaattttaaatt | 7089 |
rs531153 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | TLE2 | GRCh38.p7 | 19:2998080 | TCCATCTCAAAAAAA[C/G]AAACACGTCACTCTG | 7089 |
rs568827 | snp | A/C | 0.152667 | 0.230274 | intron-variant | TLE2 | GRCh38.p7 | 19:3001649 | ACCTACTGGCTGTTT[A/C]ATTTTTTTGTAGAGA | 7089 |
rs692919 | snp | C/T | 0.481396 | 0.0946345 | intron-variant | TLE2 | GRCh38.p7 | 19:3000164 | gcaagctccacctcc[C/T]gggttcatgccattc | 7089 |
rs818433 | snp | C/G/T | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3008641 | tttttagcagagaca[C/G/T]ggtttcaccatgttg | 7089 |
rs818436 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3018691 | ggaggcggaggttgc[A/G]gtgagccaagatcac | 7089 |
rs902715 | snp | A/T | 0.426201 | 0.177351 | intron-variant | TLE2 | GRCh38.p7 | 19:3034635 | GGAGGCTGGGGGAGA[A/T]GGCTTTTGCAGGAGA | 7089 |
rs902716 | snp | C/G | 0.426047 | 0.177503 | intron-variant | TLE2 | GRCh38.p7 | 19:3034610 | AGGAGACAGTTTTTG[C/G]GTTGGGCCTTGAAAA | 7089 |
rs953155 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | TLE2 | GRCh38.p7 | 19:3023145 | ctgcaacctccaccc[C/T]ccgggttcaagcaat | 7089 |
rs953156 | snp | C/T | 0.509615 | 0.0938218 | intron-variant | TLE2 | GRCh38.p7 | 19:3023276 | CTCCTGACCTCATGA[C/T]CCGCACGCCTTGGCC | 7089 |
rs963178 | snp | C/T | 0.294064 | 0.246086 | intron-variant | TLE2 | GRCh38.p7 | 19:3033939 | GGTGTCTCAGAGCCC[C/T]GGAAGCCAGAGGTGT | 7089 |
rs963179 | snp | C/T | 0.49998 | 0.00319482 | intron-variant | TLE2 | GRCh38.p7 | 19:3033833 | atggggggtgggggt[C/T]gggtctcgctatgtt | 7089 |
rs1058721 | snp | A/C/T | 0 | 0 | utr-variant-3-prime | TLE2 | GRCh38.p7 | 19:2997736 | AACCGTACATCCCAT[A/C/T]TGCTCTCTGGCCAAC | 7089 |
rs1058723 | snp | C/T | 0 | 0 | utr-variant-3-prime | TLE2 | GRCh38.p7 | 19:2997729 | CATCCCATCTGCTCT[C/T]TGGCCAACGGCTTCA | 7089 |
rs1615419 | snp | C/T | 0.499295 | 0.0187567 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030120 | ACAGCGTTCATGCAC[C/T]ATCTCATTTAAGTGC | 7089 |
rs1617345 | snp | C/G | 0.499234 | 0.0195537 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029828 | GCCTGGGCAACACAG[C/G]GAGACCCTATCTCTG | 7089 |
rs1654674 | snp | C/G | 0.349671 | 0.229272 | intron-variant | TLE2 | GRCh38.p7 | 19:3036516 | GTGGCCCGGCAGTTC[C/G]GCTGGAGGGGGCGGT | 7089 |
rs1654675 | snp | C/G | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3036475 | TGGCGGTGTCGGAAG[C/G]CAAAGGCTTGGCCTC | 7089 |
rs1654677 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | TLE2 | GRCh38.p7 | 19:3034553 | GAGGGGGAGGGAATT[C/G]CAGGAAGAGATAACA | 7089 |
rs1654678 | snp | C/T | 0.152334 | 0.230133 | intron-variant | TLE2 | GRCh38.p7 | 19:3034079 | TGAGATCTGGGGGAC[C/T]TCTAGGGGAGATGCC | 7089 |
rs1654679 | snp | A/G | 0.4711 | 0.116682 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030420 | GTTGATTGACTTCAC[A/G]AACCTCTCCTGAGGT | 7089 |
rs1688114 | snp | A/G | 0.118584 | 0.212673 | intron-variant | TLE2 | GRCh38.p7 | 19:3037789 | TTTGAAGATTCTATT[A/G]TTAATCTTGTGTTCC | 7089 |
rs1688115 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TLE2 | GRCh38.p7 | 19:3037371 | GCACTGCTCAAATGA[A/G]GCAACTCCTATGCAT | 7089 |
rs1688118 | snp | C/G | 0.111576 | 0.20818 | intron-variant | TLE2 | GRCh38.p7 | 19:3034536 | aggaagagataacaa[C/G]cagggaaaggctcag | 7089 |
rs1688126 | snp | A/C | 0.0876345 | 0.190099 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030972 | GCTTTAAATTTGATA[A/C]GGGCttttttttttt | 7089 |
rs1688127 | snp | C/T | 0.492287 | 0.0616198 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030440 | TATGCATTTAGTACA[C/T]GTTTGTTGATTGACT | 7089 |
rs1688128 | snp | A/G | 0.499203 | 0.0199521 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030170 | AGGAACACAATTCCC[A/G]TCTGTGGAAGTTTGC | 7089 |
rs1688134 | snp | C/T | 0.498133 | 0.030494 | intron-variant | TLE2 | GRCh38.p7 | 19:3044903 | cttcacagcattttt[C/T]gctccgcacaattta | 7089 |
rs1826321 | snp | C/T | 0.478603 | 0.101197 | intron-variant | TLE2 | GRCh38.p7 | 19:3008500 | ccgtgccattgcact[C/T]cagcctgggcaatag | 7089 |
rs1844880 | snp | G/T | 0.497245 | 0.0370121 | intron-variant | TLE2 | GRCh38.p7 | 19:3014649 | TGGAGGCAGGGGCAT[G/T]ACCACAATGAGCTCT | 7089 |
rs1975184 | snp | C/T | 0.236144 | 0.249616 | intron-variant | TLE2 | GRCh38.p7 | 19:3025707 | CAGGCAGAGGCAAAG[C/T]CCGTGGCCATTGTAT | 7089 |
rs1975185 | snp | G/T | 0.445328 | 0.156035 | intron-variant | TLE2 | GRCh38.p7 | 19:3023812 | CTCCACCTCCTGGGT[G/T]CAAGCGATTCTCATG | 7089 |
rs1975186 | snp | C/T | 0.445328 | 0.156035 | intron-variant | TLE2 | GRCh38.p7 | 19:3023753 | AGGCGTGCACCACCA[C/T]GCCCGGCTAATTTTT | 7089 |
rs1975187 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3023721 | tatttttagtagaga[C/T]gggtctccctatgtt | 7089 |
rs1982083 | snp | C/T | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3027612 | TTCTGAAGACAGTAT[C/T]TAGCAGTTGGAGCGT | 7089 |
rs2013994 | snp | A/G | 0.499921 | 0.00629039 | intron-variant | TLE2 | GRCh38.p7 | 19:3023059 | TCAAAAAAAAAAAAA[A/G]AAGATTAGGTAAAAT | 7089 |
rs2015037 | snp | A/T | 0.445064 | 0.156365 | intron-variant | TLE2 | GRCh38.p7 | 19:3023120 | TTGCAGTGAGCCGAG[A/T]TCGCACCATTGCACT | 7089 |
rs2116964 | snp | A/G | 0.417521 | 0.185571 | intron-variant | TLE2 | GRCh38.p7 | 19:3023672 | CCCCCGGACTCAAGC[A/G]ATCCGCCCGTGTCAG | 7089 |
rs2163867 | snp | C/T | 0.406296 | 0.19512 | intron-variant | TLE2 | GRCh38.p7 | 19:3023863 | GCTCTGTTACCCAGG[C/T]TGGAGTGCAGTGGCA | 7089 |
rs2163868 | snp | C/T | 0.445724 | 0.155538 | intron-variant | TLE2 | GRCh38.p7 | 19:3023552 | CGTGAAAGATAGTTC[C/T]ACTTCAGAGTGGATA | 7089 |
rs2201123 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | TLE2 | GRCh38.p7 | 19:3023147 | gaattgcttgaaccc[C/G]gggggtggaggttgc | 7089 |
rs2228175 | snp | C/T | 9.08142e-05 | 0.00673787 | synonymous-codon | TLE2 | GRCh38.p7 | 19:3011023 | TTCCACGGACAGCGT[C/T]GGTGAGCACCTTGCC | 7089 |
rs2238621 | snp | A/G | 0.477853 | 0.102875 | intron-variant | TLE2 | GRCh38.p7 | 19:3005278 | TTAGAGAGTTACAGG[A/G]GAAGCCTGTGGATGT | 7089 |
rs2288950 | snp | C/G | 0.479016 | 0.100258 | intron-variant | TLE2 | GRCh38.p7 | 19:3028873 | GGCACCCGGTGAGTG[C/G]GGACTGCGGGGAGGG | 7089 |
rs2304251 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3025269 | CTCGCTCAGCTGAGC[A/T]CGCAGCCTGGTGGGG | 7089 |
rs2542227 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3003448 | ttcatgaccagcctg[A/G]ccaacatggcgaaaa | 7089 |
rs2873158 | snp | A/G | 0.411074 | 0.191194 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048767 | tgatccgtccgcctc[A/G]gcctcccaaaatgct | 7089 |
rs2909198 | snp | A/G | 0.487995 | 0.0765403 | intron-variant | TLE2 | GRCh38.p7 | 19:2998275 | tgtgtgtgtgtgtgt[A/G]taatttttttttttt | 7089 |
rs3050847 | in-del | -/AT | 0.441841 | 0.160303 | intron-variant | TLE2 | GRCh38.p7 | 19:3006238 | AAAGGGGTGGGGCTC[-/AT]TGGCCAATCTGAATT | 7089 |
rs3760961 | snp | A/G | 0.335559 | 0.234904 | intron-variant | TLE2 | GRCh38.p7 | 19:3013376 | ACTATGTTTATTTCC[A/G]TGGGATTTCCTATTG | 7089 |
rs3760963 | snp | A/G | 0.0929672 | 0.194527 | intron-variant | TLE2 | GRCh38.p7 | 19:3013626 | TGCTTCGGGGCCCCC[A/G]GGATGAATAAAGTGA | 7089 |
rs3760965 | snp | C/T | 0.403684 | 0.197183 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030054 | TCAAGCCTCTCTCTT[C/T]GGCCTTCCAAAGTGC | 7089 |
rs3816055 | snp | C/G | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3024779 | GCTGTTTTCCCCCTT[C/G]ATGGGAAGCAAGGCA | 7089 |
rs3831629 | in-del | -/AAAAC | 0.330947 | 0.236533 | intron-variant | TLE2 | GRCh38.p7 | 19:3008084 | GAAACTCAGTCTCAG[-/AAAAC]AAAACAAAACAAAAC | 7089 |
rs3834644 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3013533 | GGTTTAAAAAAAAAA[-/A]GCACAGGGAAAGGGT | 7089 |
rs3894589 | snp | C/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3000841 | ttttttttttttttt[C/T]ccaagaaagggtctt | 7089 |
rs4061734 | in-del | -/A/AA | 0.483636 | 0.0889627 | intron-variant | TLE2 | GRCh38.p7 | 19:3000824 | aaaaaaaaaaaaaaa[-/A/AA]NGGGAGAGGCCAGAC | 7089 |
rs4257327 | snp | A/C | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:2999542 | accatcctggctaac[A/C]cggtgaaaccccgtc | 7089 |
rs4270285 | snp | A/G | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3043501 | CAGCTTTTAATATCA[A/G]AAAACATCTACCTGG | 7089 |
rs4361051 | snp | C/T | 0.0944967 | 0.195752 | intron-variant | TLE2 | GRCh38.p7 | 19:2999595 | agccaggtgtggtgg[C/T]gggtacctggagtcc | 7089 |
rs4399658 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3025350 | ACAGATACACCACCC[A/G]CCAGACGCACACCCG | 7089 |
rs4522524 | snp | C/T | 0.478685 | 0.10101 | intron-variant | TLE2 | GRCh38.p7 | 19:3008599 | gggattacaggtgcc[C/T]gccaccacgtccggc | 7089 |
rs4613189 | snp | A/C | 0.272511 | 0.248984 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997155 | TCAACATGGAGAAAC[A/C]TTGTCTCTACTAAAA | 7089 |
rs4616404 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | TLE2 | GRCh38.p7 | 19:3023566 | TAGAACTATCTTTCA[C/T]GTCTCTCTGAAGAGA | 7089 |
rs4806894 | snp | A/C | 0.367503 | 0.220665 | intron-variant | TLE2 | GRCh38.p7 | 19:3022356 | GTGAAACCACCCCCC[A/C]ACCCCATCTACAAAA | 7089 |
rs4806895 | snp | C/T | 0.451234 | 0.14834 | intron-variant | TLE2 | GRCh38.p7 | 19:3022477 | gagattgcagtgagc[C/T]gagatcgtgccattg | 7089 |
rs4806896 | snp | C/T | 0.445064 | 0.156365 | intron-variant | TLE2 | GRCh38.p7 | 19:3024053 | CAGGCTGGAGTGCAG[C/T]GGCGCAATCTCTGCT | 7089 |
rs4806898 | snp | A/G | 0.499846 | 0.00878459 | intron-variant | TLE2 | GRCh38.p7 | 19:3033160 | tgggattacagacat[A/G]caccaagcctggcta | 7089 |
rs4807385 | snp | A/G | 0.444799 | 0.156695 | intron-variant | TLE2 | GRCh38.p7 | 19:3016725 | GTGAGGATGGGAAGA[A/G]GGGTCCAAGGTCATG | 7089 |
rs4807386 | snp | G/T | 0.267636 | 0.249377 | intron-variant | TLE2 | GRCh38.p7 | 19:3016954 | CAGCTAATTTTGTAT[G/T]TTTAGTAGAGATATG | 7089 |
rs4807388 | snp | C/G | 0.366679 | 0.221102 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031514 | TGTTTATTGTTTATA[C/G]AGACAAGGTCTCACT | 7089 |
rs4807389 | snp | C/T | 0.361263 | 0.223876 | intron-variant | TLE2 | GRCh38.p7 | 19:3038376 | accacactcagctaa[C/T]ttaaaaaaaattttt | 7089 |
rs5826787 | in-del | -/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3000825 | TTTTTTTTTTTTTTT[-/T]TCCAAGAAAGGGTCT | 7089 |
rs7246701 | snp | A/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3038494 | ctgggattacaggtg[A/T]gaaacactgtgtcca | 7089 |
rs7246941 | snp | C/G | 0.437542 | 0.165312 | intron-variant | TLE2 | GRCh38.p7 | 19:3018233 | agttcccgggctcaa[C/G]tgattgtcccatctc | 7089 |
rs7249797 | snp | A/T | 0.357024 | 0.225933 | intron-variant | TLE2 | GRCh38.p7 | 19:3006229 | TTGCAAGTCCAATTC[A/T]GATTGGCCAGAGCCC | 7089 |
rs7249809 | snp | A/G | 0.49931 | 0.0185575 | intron-variant | TLE2 | GRCh38.p7 | 19:3020693 | TGAGTTCTCTTTGGC[A/G]TCTGGCCTCTCAGCA | 7089 |
rs7251484 | snp | A/G | 0.499464 | 0.016365 | intron-variant | TLE2 | GRCh38.p7 | 19:3024437 | aatttctgtccccat[A/G]aaactctcactcccc | 7089 |
rs7251701 | snp | C/G/T | 0.000169986 | 0.00921759 | intron-variant | TLE2 | GRCh38.p7 | 19:3024996 | ctcccttcccctcct[C/G/T]cccccaccccCAGGC | 7089 |
rs7254661 | snp | C/T | 0.499942 | 0.00539106 | intron-variant | TLE2 | GRCh38.p7 | 19:3024315 | ctggccGAATTACAG[C/T]ccattttaaccattt | 7089 |
rs7258703 | snp | A/G | 0.097727 | 0.198275 | intron-variant | TLE2 | GRCh38.p7 | 19:3017931 | TCCACGGCGCCAGAG[A/G]GTACAGCCCTCCAGT | 7089 |
rs7258928 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3047172 | CCCTCCCCTCCCCCT[A/G]CCCTCCCCCGTCCTC | 7089 |
rs7259652 | snp | C/T | 0.125528 | 0.21681 | intron-variant | TLE2 | GRCh38.p7 | 19:3017960 | GTTTATAAAGCCCCC[C/T]GCCCCCACCACCCCA | 7089 |
rs7260031 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | TLE2 | GRCh38.p7 | 19:3004501 | aaaattagccgagca[C/T]ggtggtgcgttcctg | 7089 |
rs7507807 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3028397 | GCTGAGAAGAAGAGA[A/G]AGGGCAAGGGGCTCC | 7089 |
rs8100567 | snp | C/T | 0.445592 | 0.155704 | intron-variant | TLE2 | GRCh38.p7 | 19:3022434 | ctcgggaggctgagg[C/T]ggaagaatcgcttga | 7089 |
rs8101205 | snp | A/C | 0.279927 | 0.248202 | intron-variant | TLE2 | GRCh38.p7 | 19:3039225 | atcctttccccactc[A/C]aaaaaaaaaaaaaaa | 7089 |
rs8103226 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3036892 | GTTGGGGTTAGGGAG[G/T]ATCAGAGCTGGGGGT | 7089 |
rs8104169 | snp | A/T | 0.494057 | 0.0541878 | intron-variant | TLE2 | GRCh38.p7 | 19:3044816 | TAGTAGAAACCCAAA[A/T]CAGACAAACTCTCTT | 7089 |
rs8106301 | snp | A/G | 0.306679 | 0.24349 | intron-variant | TLE2 | GRCh38.p7 | 19:3021360 | cagtgagccaagatc[A/G]tgccatgcactcccg | 7089 |
rs8106924 | snp | C/G | 0.49934 | 0.0181589 | intron-variant | TLE2 | GRCh38.p7 | 19:3021144 | gagcgtggtgactca[C/G]acctgtaatcccagc | 7089 |
rs8106981 | snp | A/G | 0.114036 | 0.209795 | intron-variant | TLE2 | GRCh38.p7 | 19:3000217 | gctgggactacaggc[A/G]cccaccaccacgcct | 7089 |
rs8110424 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3021270 | attagtcaggcatgg[C/T]ggcatgcacctgtaa | 7089 |
rs8110519 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE2 | GRCh38.p7 | 19:3021342 | cccgggagttagaga[C/T]tgcagtgagccaaga | 7089 |
rs8111113 | snp | C/T | 0.284733 | 0.247575 | intron-variant | TLE2 | GRCh38.p7 | 19:3038088 | gatcacaccactgca[C/T]tccagcctgggggac | 7089 |
rs8111622 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | TLE2 | GRCh38.p7 | 19:3010295 | cttgaacctgggagc[A/G]ggaggttgcagtgag | 7089 |
rs8111765 | snp | A/T | 0.118584 | 0.212673 | intron-variant | TLE2 | GRCh38.p7 | 19:3022542 | tcaaaaaaaaaaaaa[A/T]tttttttaaggaaaa | 7089 |
rs9304902 | snp | A/G | 0.39214 | 0.205661 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030372 | CCTTCAGGCCCACCC[A/G]GGGAGTGGGAAGTTC | 7089 |
rs10401433 | snp | C/T | 0.326035 | 0.238157 | intron-variant | TLE2 | GRCh38.p7 | 19:3040379 | ACAGTCTCGCTCTGT[C/T]GACCAGGCTGGAGTG | 7089 |
rs10404009 | snp | C/T | 0.267636 | 0.249377 | intron-variant | TLE2 | GRCh38.p7 | 19:3035513 | CTGGCTAGGGTTTTA[C/T]GTTGTGGATGTGGGT | 7089 |
rs10404481 | snp | A/C | 0.20511 | 0.245937 | intron-variant | TLE2 | GRCh38.p7 | 19:3035768 | AGGAGGCACTGGGAT[A/C]AGTAGGGCCAATCGG | 7089 |
rs10406479 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3018123 | CAGGGCCTTGCAGCC[A/G]CTCTCATTGATCCCC | 7089 |
rs10407150 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | TLE2 | GRCh38.p7 | 19:3018485 | tttagtagagacaag[A/G]tttcaccacgttgac | 7089 |
rs10407820 | snp | G/T | 0.367913 | 0.220446 | intron-variant | TLE2 | GRCh38.p7 | 19:3040354 | AACGTTTGTTTGTTT[G/T]TTTTTTAAGACAGTC | 7089 |
rs10407845 | snp | A/G | 0.213635 | 0.247341 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048875 | ctggagttcagtggc[A/G]cgatcatggctcctt | 7089 |
rs10408306 | snp | C/T | 0.322721 | 0.23919 | intron-variant | TLE2 | GRCh38.p7 | 19:3040556 | GTTACCCAGGCTGGT[C/T]TCGAACTCCTGGCCT | 7089 |
rs10408740 | snp | C/T | 0.364817 | 0.222075 | intron-variant | TLE2 | GRCh38.p7 | 19:3010650 | GAGCACTGTCATTCC[C/T]CAGATTACTGATGGG | 7089 |
rs10408957 | snp | A/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041011 | tatatatatatatat[A/T]tattttttttttttt | 7089 |
rs10408961 | snp | A/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041013 | tatatatatatatat[A/T]ttttttttttttttt | 7089 |
rs10410014 | snp | A/C | 0.030278 | 0.119257 | intron-variant | TLE2 | GRCh38.p7 | 19:3011749 | cagctacttgggagg[A/C]taaggcaggagaatt | 7089 |
rs10412216 | snp | A/G | 0.497211 | 0.037236 | intron-variant | TLE2 | GRCh38.p7 | 19:3036519 | GCCCCCTCCAGCCGA[A/G]CTGCCGGGCCACCAG | 7089 |
rs10412849 | snp | A/G | 0.345482 | 0.231048 | intron-variant | TLE2 | GRCh38.p7 | 19:3024626 | TACCCATCATCTCCA[A/G]CACCCTGGGTGTATG | 7089 |
rs10413959 | snp | A/C | | | intron-variant | TLE2 | GRCh38.p7 | 19:3024419 | tcccatcttcccaaa[A/C]tgaatttctgtcccc | 7089 |
rs10414425 | snp | A/G | 0.350327 | 0.228986 | intron-variant | TLE2 | GRCh38.p7 | 19:3012107 | aaaaattagccaggc[A/G]tggtggcacgtgcct | 7089 |
rs10416487 | snp | C/T | 0.498182 | 0.0300969 | intron-variant | TLE2 | GRCh38.p7 | 19:3020230 | GACAGAGCGAGACTC[C/T]GTCTCAAGAAAAAAT | 7089 |
rs10416897 | snp | C/G | 0.466204 | 0.125522 | intron-variant | TLE2 | GRCh38.p7 | 19:3000012 | cactccagcctggga[C/G]acagagcaagattct | 7089 |
rs10417381 | snp | C/T | 0.457504 | 0.139435 | intron-variant | TLE2 | GRCh38.p7 | 19:3036352 | GCGCTCTCCCGCCCG[C/T]CGCCTCCCTCCCGCC | 7089 |
rs10417792 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | TLE2 | GRCh38.p7 | 19:3020881 | acttgaggtcaggag[C/T]tcaagaccagcctgg | 7089 |
rs10418178 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | TLE2 | GRCh38.p7 | 19:3042897 | AGACAGACATTACCC[A/G]GGAGAGAAAGTTAGA | 7089 |
rs10418394 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | TLE2 | GRCh38.p7 | 19:3045227 | tcaaaataataaaaa[C/T]aaagaatgcaggaaa | 7089 |
rs10419127 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | TLE2 | GRCh38.p7 | 19:3016707 | ATGGCTAGGCGAACG[A/G]AAGTGAGGATGGGAA | 7089 |
rs10423018 | snp | C/T | 0.067446 | 0.170804 | intron-variant | TLE2 | GRCh38.p7 | 19:3042560 | CCAAGCTGGAGACTT[C/T]GAAGGACAGAGGGAG | 7089 |
rs10423211 | snp | C/T | 0.373196 | 0.217538 | intron-variant | TLE2 | GRCh38.p7 | 19:3012528 | AGCCACTGTTGAGAT[C/T]CTTGAACAACAAGGA | 7089 |
rs10424408 | snp | A/G | 0.351635 | 0.228408 | intron-variant | TLE2 | GRCh38.p7 | 19:3038442 | ggtcttcaactcctg[A/G]gctcaagcagtcctc | 7089 |
rs10425504 | snp | A/C | 0.20111 | 0.245173 | intron-variant | TLE2 | GRCh38.p7 | 19:3038271 | ggagtgcagtgccac[A/C]gtcatagctcactgc | 7089 |
rs10427056 | snp | C/T | 0.15698 | 0.23205 | intron-variant | TLE2 | GRCh38.p7 | 19:3040200 | CATGGACTCCCGTCT[C/T]TATCTCCACCCTCCC | 7089 |
rs10603560 | in-del | -/A | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3016607 | GCAAGACTCAGTCTC[-/A]AAAAAAAAAAAAAAA | 7089 |
rs10664438 | in-del | -/T/TTT | | | intron-variant | TLE2 | GRCh38.p7 | 19:3032953 | TTGTTTTTTTTTTTT[-/T/TTT]GACGGAGTCATGCTC | 7089 |
rs11084989 | snp | A/C | 0.328616 | 0.237317 | intron-variant | TLE2 | GRCh38.p7 | 19:3008695 | ACCTAAAGTGATCCA[A/C]CTGCCTCAGCCTTCC | 7089 |
rs11084990 | snp | G/T | 0.335101 | 0.23507 | intron-variant | TLE2 | GRCh38.p7 | 19:3009222 | GGCTCTAGGCCAGGG[G/T]TCTGAAAACTCCAGC | 7089 |
rs11084991 | snp | C/T | 0.271702 | 0.249056 | intron-variant | TLE2 | GRCh38.p7 | 19:3021128 | AAGGGGGGGGGGTGC[C/T]GAGCGTGGTGACTCA | 7089 |
rs11084992 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | TLE2 | GRCh38.p7 | 19:3023146 | tgcaacctccacccc[A/C]cgggttcaagcaatt | 7089 |
rs11084993 | snp | C/T | 0.423881 | 0.179625 | intron-variant | TLE2 | GRCh38.p7 | 19:3042736 | TCCCCAGAGATCCTA[C/T]GTAGAAGCTGTTCTC | 7089 |
rs11379215 | in-del | -/A | 0.487495 | 0.0780784 | intron-variant | TLE2 | GRCh38.p7 | 19:3017241 | TCCCAGGTCCAAGTG[-/A]ATTCTCCTGCCTTGA | 7089 |
rs11438908 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3009895 | TCTCTCTCTTTTTTT[C/T]TTTTGTTTGAGATGG | 7089 |
rs11665669 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3010138 | ggaggccgaggtggg[C/T]ggatcacctgaggtc | 7089 |
rs11665900 | snp | C/T | 0.32768 | 0.237625 | intron-variant | TLE2 | GRCh38.p7 | 19:3010805 | AACCCCCGACTAAGC[C/T]GCTTCCACTCTCCAG | 7089 |
rs11666683 | snp | C/T | 0.160938 | 0.233598 | intron-variant | TLE2 | GRCh38.p7 | 19:3031910 | cagctcctaccaTAG[C/T]GTGTGGCtttttgtt | 7089 |
rs11667215 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | TLE2 | GRCh38.p7 | 19:3014275 | ccatagcgaggacta[C/T]ataaAGGCTTGGTTT | 7089 |
rs11667518 | snp | A/G | 0.112983 | 0.209108 | intron-variant | TLE2 | GRCh38.p7 | 19:3045451 | CCAACTCTGCCTGGA[A/G]TCGGTCTTTCAAGTC | 7089 |
rs11667530 | snp | C/T | 0.29175 | 0.246489 | intron-variant | TLE2 | GRCh38.p7 | 19:3032101 | atgcccagctaattt[C/T]ttttgtattattagt | 7089 |
rs11670809 | snp | A/G | 0.0807149 | 0.183963 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048088 | tacaaaaaattagcc[A/G]ggtgtggtggcgggc | 7089 |
rs11672228 | snp | A/C | 0.452473 | 0.146644 | intron-variant | TLE2 | GRCh38.p7 | 19:2998406 | tctcgaactcccaag[A/C]agctgggattgcagg | 7089 |
rs11672436 | snp | A/G | 0.327211 | 0.237778 | intron-variant | TLE2 | GRCh38.p7 | 19:3046731 | CAGAATGGGGGAGGG[A/G]GGCTGGGAGAATGGT | 7089 |
rs12052045 | snp | C/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3040768 | caacctcccaagtag[C/G]tgagaccacaatcgt | 7089 |
rs12052132 | snp | C/G | 0.25912 | 0.249834 | intron-variant | TLE2 | GRCh38.p7 | 19:3039562 | AGTAGCTCCCCTCCT[C/G]CTACCTGCTCAGCTT | 7089 |
rs12104392 | snp | G/T | 0.0970103 | 0.197722 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049266 | CTCAGGGTCTTTGTG[G/T]GGGAACTGGGGTAGG | 7089 |
rs12460154 | snp | C/T | 0.333722 | 0.235565 | intron-variant | TLE2 | GRCh38.p7 | 19:3009970 | GCTCACTGAAACCTC[C/T]GCCTCCTGGGTTCAA | 7089 |
rs12461133 | snp | C/G | 0.278133 | 0.248412 | intron-variant | TLE2 | GRCh38.p7 | 19:3008598 | TGGGATTACAGGTGC[C/G]CGCCACCACGTCCGG | 7089 |
rs12461656 | snp | A/G | 0.333722 | 0.235565 | intron-variant | TLE2 | GRCh38.p7 | 19:3009954 | CAGTGGCGCGATCTC[A/G]GCTCACTGAAACCTC | 7089 |
rs12461752 | snp | C/G | 0.33533 | 0.234987 | intron-variant | TLE2 | GRCh38.p7 | 19:3009836 | CATAGCCTGGGACAC[C/G]TCCAGACCTCTGCAC | 7089 |
rs12461758 | snp | C/T | 0.334871 | 0.235153 | intron-variant | TLE2 | GRCh38.p7 | 19:3009872 | TTCCTCCAGTGGACA[C/T]GACTTTCTCTCTCTC | 7089 |
rs12610765 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3021115 | aaaaaaaaaaaaaaa[A/G]GGGGGGGGGTgctga | 7089 |
rs12611189 | snp | C/T | 0.333952 | 0.235483 | intron-variant | TLE2 | GRCh38.p7 | 19:3042517 | GGAGGGAGGCGCCAA[C/T]GAAGAGATCCAGGGA | 7089 |
rs12971668 | snp | A/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041015 | tatatatatatatat[A/T]ttttttttttttttt | 7089 |
rs12971670 | snp | A/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041017 | tatatatatatattt[A/T]ttttttttttttttt | 7089 |
rs12971833 | snp | C/G | 0.209997 | 0.246779 | intron-variant | TLE2 | GRCh38.p7 | 19:3042354 | gagagggagggggcg[C/G]aggagggACGGGCTT | 7089 |
rs12972232 | snp | A/G | 0.193802 | 0.243602 | intron-variant | TLE2 | GRCh38.p7 | 19:3019662 | GACCTGGGAGTGGGC[A/G]TCTCCCCATGGCGGG | 7089 |
rs12973835 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:2998695 | tgggattacaagcgt[A/G]agccaccgcgcccgg | 7089 |
rs12975163 | snp | A/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3043641 | cgtctctactaaaaa[A/T]acaaaaaaaaaaaaa | 7089 |
rs12976222 | snp | A/C | 0.233818 | 0.249476 | intron-variant | TLE2 | GRCh38.p7 | 19:3044286 | CCATGGAGGATCTCG[A/C]TAATCGCACATCTGG | 7089 |
rs12978885 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3001786 | ggctTAAATTTCTTT[A/C/T]Ctttctttttttttt | 7089 |
rs12979422 | snp | A/G | 0.336474 | 0.234568 | intron-variant | TLE2 | GRCh38.p7 | 19:3011662 | tgaggccagcctggc[A/G]aacatggtgaaaacc | 7089 |
rs12980624 | snp | C/T | 0.332568 | 0.235971 | intron-variant | TLE2 | GRCh38.p7 | 19:3011414 | GCATGTGCCTGTGAT[C/T]CCAGCTACTTGGGAG | 7089 |
rs12981498 | snp | C/G | 0.0941369 | 0.195465 | intron-variant | TLE2 | GRCh38.p7 | 19:3022176 | gcctcagcctcccga[C/G]tagctgggattacag | 7089 |
rs12981832 | snp | A/G | 0.340333 | 0.233109 | intron-variant | TLE2 | GRCh38.p7 | 19:3011567 | TCTCAAAACAACAAC[A/G]GGCCAGGCGCAGTGG | 7089 |
rs12982139 | snp | A/G | 0.355525 | 0.226637 | intron-variant | TLE2 | GRCh38.p7 | 19:2999555 | acacggtgaaacccc[A/G]tctctactaaaaata | 7089 |
rs12982887 | snp | A/C | | | intron-variant | TLE2 | GRCh38.p7 | 19:3043643 | tctctactaaaaata[A/C]aaaaaaaaaaaaaaa | 7089 |
rs12984256 | snp | C/T | 0.422944 | 0.180528 | intron-variant | TLE2 | GRCh38.p7 | 19:3021968 | cccagtactttagga[C/T]gctggagtgggagga | 7089 |
rs12984592 | snp | A/G | 0.113334 | 0.209338 | intron-variant | TLE2 | GRCh38.p7 | 19:3024599 | TAACTTTCATCAGGT[A/G]CTGAGTAAGCGTACC | 7089 |
rs12984707 | snp | A/C | 0.0733688 | 0.176922 | intron-variant | TLE2 | GRCh38.p7 | 19:3015483 | CAACTGGAGTTAAGC[A/C]TTGCATTACAGGATC | 7089 |
rs12984805 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3001054 | gaggtggctgggtca[C/T]ttgaggtcaggagtt | 7089 |
rs12984941 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | TLE2 | GRCh38.p7 | 19:3015547 | AGCTATGGGAGGCTC[C/T]GGAGTGAGAGAATTA | 7089 |
rs12985110 | snp | C/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3001875 | tgatcttggctcact[C/G]cgacctccacctccc | 7089 |
rs12985412 | snp | C/G | 0.112983 | 0.209108 | intron-variant | TLE2 | GRCh38.p7 | 19:3024876 | GGCCTCAGGGCTGCG[C/G]GACTACTGCAGTGAA | 7089 |
rs13343466 | snp | A/G | 0.253824 | 0.249971 | intron-variant | TLE2 | GRCh38.p7 | 19:3026403 | cagtgagccaagatc[A/G]ggtcattgcactcca | 7089 |
rs13345197 | snp | A/G | 0.470327 | 0.118136 | intron-variant | TLE2 | GRCh38.p7 | 19:2999761 | aaaaCagctgggcgc[A/G]gtggctcacgcctgt | 7089 |
rs13346985 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | TLE2 | GRCh38.p7 | 19:3022987 | gtggagctggccctc[C/G]agctgcagtttgcta | 7089 |
rs28366705 | snp | C/G | 0.0796608 | 0.182988 | intron-variant | TLE2 | GRCh38.p7 | 19:3034632 | CTGTCTCCTGCAAAA[C/G]CCTTCTCCCCCAGCC | 7089 |
rs28389483 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3010376 | TCTCAAAAAAAAAGG[A/G]AAAAAAAAAACAAAA | 7089 |
rs28632147 | snp | C/T | 0.36606 | 0.221428 | intron-variant | TLE2 | GRCh38.p7 | 19:3041095 | ACAGTGGCGAGATCT[C/T]GGCTTACTGCAACCT | 7089 |
rs33926228 | in-del | -/T | | | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049573 | GAGCCAAAGATAATC[-/T]TTTTTTTTTTTTTTT | 7089 |
rs34088929 | snp | A/T | 0.0685596 | 0.171987 | intron-variant | TLE2 | GRCh38.p7 | 19:3027345 | CAGGGCCTGGAGAAC[A/T]ATCTTGGAACCTTCC | 7089 |
rs34098191 | in-del | -/C/CTT | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3023058 | ATTTTACCTAATCTT[-/C/CTT]TTTTTTTTTTTTTTG | 7089 |
rs34102685 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3011544 | CAAAAAAAAAAAAAA[-/A]GACTCTGTCTCAAAA | 7089 |
rs34168841 | in-del | -/T/TT | 0.375 | 0.216506 | intron-variant | TLE2 | GRCh38.p7 | 19:3008456 | TCTTTTTTTTTTTTT[-/T/TT]GAGACTGAGTCTCGC | 7089 |
rs34181478 | snp | C/T | 0.499515 | 0.0155675 | intron-variant | TLE2 | GRCh38.p7 | 19:3026869 | GGTCTATCTCAGAAC[C/T]CTGAGGTCTATCTCT | 7089 |
rs34251949 | in-del | -/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3043387 | TTTTTTTTTTTTTTT[-/T]GAGATGGTCTCGAAC | 7089 |
rs34278935 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030575 | AGTACCTAATGGTAC[-/C]TAAGGGTTAGGGTTA | 7089 |
rs34314962 | snp | C/T | 0.0659589 | 0.169201 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031094 | ACAGATCCCTGCCCT[C/T]TCTGAGTTTGTGGGA | 7089 |
rs34363860 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3021113 | AAAAAAAAAAAAAAA[-/A]AGGGGGGGGGGTGCT | 7089 |
rs34394156 | snp | C/T | 0.199564 | 0.24486 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048905 | TGCAGCCTCAAACTC[C/T]GGGGCTCAAGCAATC | 7089 |
rs34404100 | in-del | -/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029154 | GGCAGCGGCCGGGGC[-/T]GGGAGCGCGGCGAGG | 7089 |
rs34457157 | in-del | -/C | | | intron-variant | TLE2 | GRCh38.p7 | 19:3045211 | AGGTGAGACCTTGTC[-/C]TCAAAATAATAAAAA | 7089 |
rs34462423 | in-del | -/CA | 0.362523 | 0.223246 | intron-variant | TLE2 | GRCh38.p7 | 19:3036742 | TTGCTGGACAAAACT[-/CA]TTCATGAAACCCATA | 7089 |
rs34470428 | in-del | -/T | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3000841 | TTTTTTTTTTTTTTT[-/T]CCAAGAAAGGGTCTT | 7089 |
rs34532454 | in-del | -/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3011928 | ATTCTTTTTTTTTTT[-/T]AATACAGGGTCTTGC | 7089 |
rs34543305 | in-del | -/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3046095 | GTTGCCCCTAGGGGG[-/G]CAAAGAGGTCCCTGA | 7089 |
rs34559305 | in-del | -/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3005207 | AAGATGATCTGGGGG[-/G]TCTCAGTAGCCCCAC | 7089 |
rs34582294 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029744 | TGCCGGGCCCTCGCC[-/C]TCTGGGGGCCTCAGT | 7089 |
rs34595211 | snp | A/G | 0.0120332 | 0.0766276 | synonymous-codon | TLE2 | GRCh38.p7 | 19:3011032 | GCCAGCACCTTCCAC[A/G]GACAGCGTCGGTGAG | 7089 |
rs34637168 | in-del | -/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3043237 | CTCCCGCCTCAGCCT[-/G]CCCAAGTAGCTGAGA | 7089 |
rs34658846 | in-del | -/A/AA | 0.479824 | 0.098392 | intron-variant | TLE2 | GRCh38.p7 | 19:3015059 | TAAAATTCATTGCCA[-/A/AA]AAAAAAAAAAAAAAA | 7089 |
rs34669546 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3016440 | AAAAAAAAAAAAAAA[-/A]TTAGCCGGGCATGGT | 7089 |
rs34703558 | snp | C/T | 0.00132479 | 0.0257029 | synonymous-codon | TLE2 | GRCh38.p7 | 19:3005557 | CCACACGGACGGCGC[C/T]AGCTGCATTGATATT | 7089 |
rs34730609 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3010368 | AAACTCCGTCTCAAA[A/G]AAAAAGGAAAAAAAA | 7089 |
rs34783402 | in-del | -/A | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3026479 | AAAAAAAAAAAAAAA[-/A]TCTTTAGGTCTATCT | 7089 |
rs34836093 | snp | G/T | 0.078151 | 0.181571 | intron-variant | TLE2 | GRCh38.p7 | 19:3013220 | ATTAAACTCCAGGAG[G/T]TCCAACTGAAAACTT | 7089 |
rs34848381 | in-del | -/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3042846 | AAGGAAATTTTTTTT[-/T]AACGGCAGTGGGGAC | 7089 |
rs34884101 | in-del | -/A | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3010373 | CCGTCTCAAAAAAAA[-/A]GGAAAAAAAAAAACA | 7089 |
rs34956013 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030581 | TAATGGTACCTAAGG[-/G]TTAGGGTTACAAAAA | 7089 |
rs35008596 | snp | C/T | 0.121022 | 0.21416 | intron-variant | TLE2 | GRCh38.p7 | 19:3012892 | AGAGAGTGGATGGGA[C/T]GACTGTGGGGTCAGG | 7089 |
rs35017805 | snp | G/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3026699 | ATCTCAGAACCCTGA[G/T]GTCTATCTCTGAACC | 7089 |
rs35175856 | in-del | -/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3047485 | CCGACACCCCCACAA[-/G]GGGTCTTCTCGGAAG | 7089 |
rs35197329 | in-del | -/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3035399 | TTTGCGCCTCAGTTT[-/T]CCCCAGCTGCACCAT | 7089 |
rs35202557 | in-del | -/TT | | | intron-variant | TLE2 | GRCh38.p7 | 19:3023072 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAATCTCGC | 7089 |
rs35309457 | in-del | -/T | 0.495174 | 0.0488838 | intron-variant | TLE2 | GRCh38.p7 | 19:3013989 | CATCTGTAAAATGTA[-/T]TTTTTTTTTTTTTGA | 7089 |
rs35357628 | in-del | -/G | | | frameshift-variant | TLE2 | GRCh38.p7 | 19:3005446 | AGCACCTGGGAGCTG[-/G]AAGTCATGCTGCTGC | 7089 |
rs35366775 | in-del | -/C | | | intron-variant | TLE2 | GRCh38.p7 | 19:3032684 | GCTCAATAACCAGCC[-/C]TAAAGCCAGAAACCG | 7089 |
rs35438959 | in-del | -/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3023329 | GCGTGAGCCACTGGG[-/G]CTCGGCCTACCTAAA | 7089 |
rs35442589 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3043660 | AAAAAAAAAAAAAAA[-/A]TTAGCCAGGCATGGT | 7089 |
rs35467331 | snp | C/T | 0.103794 | 0.20279 | intron-variant | TLE2 | GRCh38.p7 | 19:3027124 | CCTGAGGTCTATCTC[C/T]GAACCTTGAGGTCAA | 7089 |
rs35474356 | in-del | -/C | 0.48666 | 0.0805725 | intron-variant | TLE2 | GRCh38.p7 | 19:3041929 | TGCCTTTGCGGGGGG[-/C]CCCGAGTCCCAGGGT | 7089 |
rs35493371 | in-del | -/T | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3033187 | CTAATTTTTTTTTTT[-/T]AATGGAGTCTCACTC | 7089 |
rs35540322 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | TLE2 | GRCh38.p7 | 19:3007942 | ATACAAAAATTAGCC[A/G]GCGGTGGTCCGTGCC | 7089 |
rs35580021 | snp | C/G | 0.0916144 | 0.193427 | intron-variant | TLE2 | GRCh38.p7 | 19:3000493 | CCAACCTCTGCTTTA[C/G]TACCTGGGCGGTAGG | 7089 |
rs35623428 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3007075 | AGGCGTGAGCCACCA[-/A]TGCCCAGCCTGATGC | 7089 |
rs35657071 | snp | A/G | 0 | 0 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048416 | GAGAGGAAGAGCCAG[A/G]ATTTAAATCCAGGCT | 7089 |
rs35727082 | in-del | -/C | | | intron-variant | TLE2 | GRCh38.p7 | 19:3044154 | TCCAGCCTGGGCGAC[-/C]AGAGACTCCGTCTCA | 7089 |
rs35739361 | snp | A/G | 0.187369 | 0.242028 | intron-variant | TLE2 | GRCh38.p7 | 19:3026987 | GAGGTCTATCTCAGA[A/G]CCCTGAGGTCAATCT | 7089 |
rs35741547 | in-del | -/C | | | intron-variant | TLE2 | GRCh38.p7 | 19:3044161 | TGGGCGACAGAGACT[-/C]CCGTCTCACCAAAAA | 7089 |
rs35965540 | in-del | -/G | | | frameshift-variant | TLE2 | GRCh38.p7 | 19:3011126 | GGGAGGAGTCACAGG[-/G]ATTTGGAGGCAGGAG | 7089 |
rs35973313 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041263 | ACTCTTGACCTCAAA[-/A]TTATCCACCTGCCTC | 7089 |
rs36006446 | in-del | -/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3042076 | CAGGGGAGTGAGGGG[-/G]ATTGCGGGGAGTAGG | 7089 |
rs45521535 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3016156 | GGCCAGGCCTATCTC[A/G]AACTCCTGACCTCAG | 7089 |
rs55899242 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3021803 | GACCAGGCTGGTCTT[A/G]AACTCCTGATCTCAA | 7089 |
rs55919790 | snp | C/T | 0.5 | 0.00019968 | splice-donor-variant | TLE2 | GRCh38.p7 | 19:3047562 | TATCAGTAATACTTA[C/T]TATTGTTATTATTAT | 7089 |
rs55954173 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | TLE2 | GRCh38.p7 | 19:3000969 | AGGTGTGCACCACCA[C/T]GCCCAGCTAATATTT | 7089 |
rs55998855 | in-del | -/ATATACATATATA/ATATATATATATTT/GTATATATATATATATATATATATATTT | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041014 | TATATATATATATAT[lengthTooLong]TTTTTTTTTTTTTTT | 7089 |
rs56000075 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | TLE2 | GRCh38.p7 | 19:3026010 | CCCAATACAAGGTTC[C/T]GCTCATTGATTCTAA | 7089 |
rs56131688 | snp | C/T | 0.469049 | 0.120489 | intron-variant | TLE2 | GRCh38.p7 | 19:3017615 | ACCACCACACCCAGC[C/T]AACTTTTTGTATTTT | 7089 |
rs56139778 | snp | A/C | | | intron-variant | TLE2 | GRCh38.p7 | 19:3021789 | GGTTTCACCATGTTG[A/C]CCAGGCTGGTCTTGA | 7089 |
rs56156232 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TLE2 | GRCh38.p7 | 19:3046577 | CTGACAGACACCCCC[C/T]CACCCCCCACCCCAC | 7089 |
rs56173499 | snp | C/T | | | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048042 | CGAGATCAGCCTGGC[C/T]AATATGGCGAAACCC | 7089 |
rs56196100 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3021802 | TGACCAGGCTGGTCT[C/T]GAACTCCTGATCTCA | 7089 |
rs56305743 | snp | C/T | 0.029116 | 0.117091 | intron-variant | TLE2 | GRCh38.p7 | 19:3010294 | GCTTGAACCTGGGAG[C/T]GGGAGGTTGCAGTGA | 7089 |
rs56322397 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3009889 | ACTTTCTCTCTCTCT[C/T]TTTTTCTTTTGTTTG | 7089 |
rs56378719 | snp | A/T | 0.124837 | 0.216412 | intron-variant | TLE2 | GRCh38.p7 | 19:3032098 | GCCATGCCCAGCTAA[A/T]TTTTTTTGTATTATT | 7089 |
rs56398458 | in-del | -/GTGTGT | | | intron-variant | TLE2 | GRCh38.p7 | 19:2998269 | TGTGTGTGTGTGTGT[-/GTGTGT]GTAATTTTTTTTTTT | 7089 |
rs56656741 | in-del | -/CAAA | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3012272 | CGAAAAACAAACAAA[-/CAAA]AGGCACGATCATAGC | 7089 |
rs56801494 | snp | A/C | 0.345925 | 0.230864 | intron-variant | TLE2 | GRCh38.p7 | 19:3045591 | GGAGGCCAAGGCGGG[A/C]GGATCACTTGAGGTC | 7089 |
rs57044039 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3010386 | AAAGGAAAAAAAAAA[-/A]CAAAACCCAGGCCCA | 7089 |
rs57243039 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3016386 | TGAGACCATCCTGGC[C/T]AACACGGTGAAACCC | 7089 |
rs57677219 | in-del | -/GG | | | intron-variant | TLE2 | GRCh38.p7 | 19:3021124 | AAAAAGGGGGGGGGG[-/GG]TGCTGAGCGTGGTGA | 7089 |
rs57740041 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3016470 | TGGCGGGCACTTGTA[A/G]TCCCAGCTACTTGGG | 7089 |
rs57799630 | snp | A/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:2998278 | GTGTGTGTGTGTGTA[A/T]TTTTTTTTTTTTTTT | 7089 |
rs58210754 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE2 | GRCh38.p7 | 19:3011519 | CCTGGGAGACAGAGC[A/G]ACTCCATCTCAAAAA | 7089 |
rs58422279 | snp | A/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:2998276 | GTGTGTGTGTGTGTG[A/T]AATTTTTTTTTTTTT | 7089 |
rs58528928 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TLE2 | GRCh38.p7 | 19:3002690 | ACAGGCATGCACCAT[C/T]ACGCTGGATAATCTT | 7089 |
rs58605703 | snp | A/T | 0.271162 | 0.249103 | intron-variant | TLE2 | GRCh38.p7 | 19:3020680 | TGGGCTCATTCTCTG[A/T]GTTCTCTTTGGCATC | 7089 |
rs58610901 | snp | C/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3016526 | ACCCAGGAGGCGGAG[C/G]TTACAGTGAGCCGAG | 7089 |
rs59075552 | in-del | -/T | 0.0839998 | 0.186933 | intron-variant | TLE2 | GRCh38.p7 | 19:3035260 | CGCCTGTGACTCCAT[-/T]AACTCCCCAAAATAC | 7089 |
rs59328340 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041019 | ATATATATATTTTTT[-/A]TTTTTTTTTTTTTTT | 7089 |
rs59416200 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041016 | TATATATATATATTT[-/A]TTTTTTTTTTTTTTT | 7089 |
rs59471021 | snp | A/C | 0.0759472 | 0.179459 | intron-variant | TLE2 | GRCh38.p7 | 19:3018164 | CGAGTTGGGGTCTTG[A/C]TCTGTTGCCCAGGCT | 7089 |
rs59552044 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE2 | GRCh38.p7 | 19:3011494 | CCGAGATCACGCCAC[C/T]GCACTCCAGCCTGGG | 7089 |
rs59586095 | in-del | -/G | 0.236434 | 0.249632 | intron-variant | TLE2 | GRCh38.p7 | 19:3025817 | CCCGCACCCCATAAA[-/G]GGGGGGTCTATTGCG | 7089 |
rs59922926 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TLE2 | GRCh38.p7 | 19:3024954 | GGGCGTCCTCGCCCA[A/G]ACCTACCCCCTCCCG | 7089 |
rs59931576 | snp | G/T | 0.323197 | 0.239044 | intron-variant | TLE2 | GRCh38.p7 | 19:3019988 | TAAGTGCAGGTAGAA[G/T]AGTTACAAATCAGGC | 7089 |
rs60002684 | snp | A/G | 0.337614 | 0.234145 | intron-variant | TLE2 | GRCh38.p7 | 19:3022067 | CATATATACTTATTT[A/G]AGCCGGAGTCTCACT | 7089 |
rs60203611 | snp | C/G | 0.0498117 | 0.149749 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997278 | GTTGCAGTGAGCTGA[C/G]ATCGTACCACTGTAC | 7089 |
rs60265159 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030967 | AAAAAAAAAAAAAAA[-/A]GCCCTTATCAAATTT | 7089 |
rs60331094 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | TLE2 | GRCh38.p7 | 19:3028604 | CTTTGTCGCGCCCCC[A/C]CTCCAACCGGGAGCC | 7089 |
rs60459484 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041018 | TATATATATATTTTT[-/A]TTTTTTTTTTTTTTT | 7089 |
rs60559457 | in-del | -/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3044380 | TAGGGCAGGCAGGAT[-/T]CTACAGGGCTGGCCC | 7089 |
rs60677837 | snp | C/G | 0.262159 | 0.249704 | intron-variant | TLE2 | GRCh38.p7 | 19:3021798 | ATGTTGACCAGGCTG[C/G]TCTTGAACTCCTGAT | 7089 |
rs60716314 | snp | C/T | 0.323671 | 0.238899 | intron-variant | TLE2 | GRCh38.p7 | 19:3040558 | TACCCAGGCTGGTTT[C/T]GAACTCCTGGCCTCA | 7089 |
rs60786926 | snp | A/G | 0.201727 | 0.245295 | intron-variant | TLE2 | GRCh38.p7 | 19:3037706 | AGAACTGGGCGGCTG[A/G]GGGAGAAGTCCCAGA | 7089 |
rs60883500 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | TLE2 | GRCh38.p7 | 19:3021926 | TTAATAGATTTCAGG[C/T]CGGGCGCAGTGGCTC | 7089 |
rs60898410 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031386 | TGTGTGTGTGTGTGT[-/GT]AGTACTCACTAGCTC | 7089 |
rs60902733 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE2 | GRCh38.p7 | 19:3044570 | GATTACAGGTGTGCG[C/T]CACCACGCCCGGCTA | 7089 |
rs61132194 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3016555 | AGATTGCACCACTGC[A/G]CTCCAGCCTGGGCGA | 7089 |
rs61230036 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041015 | ATATATATATATATT[-/A]TTTTTTTTTTTTTTT | 7089 |
rs61346022 | snp | A/G | 0.268724 | 0.249298 | intron-variant | TLE2 | GRCh38.p7 | 19:3022053 | TCTGTTACATTATAC[A/G]TATATACTTATTTAA | 7089 |
rs61444494 | in-del | -/A | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3004633 | AAAAAAAAAAAAAAA[-/A]GAGGAGCTTCGGAGT | 7089 |
rs61484810 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041017 | ATATATATATATTTT[-/A]TTTTTTTTTTTTTTT | 7089 |
rs61735265 | snp | C/T | 3.08752e-05 | 0.00392895 | missense | TLE2 | GRCh38.p7 | 19:3011022 | AGGCAAGGTGCTCAC[C/T]GACGCTGTCCGTGGA | 7089 |
rs61735274 | snp | C/T | 0.0495799 | 0.149438 | synonymous-codon | TLE2 | GRCh38.p7 | 19:3005476 | CAGCTGGCGGCCCTC[C/T]CGCAGGTCCCAGCAG | 7089 |
rs62125442 | snp | C/G | 0.477853 | 0.102875 | intron-variant | TLE2 | GRCh38.p7 | 19:2999109 | CAACGTGGGGAATCC[C/G]CGTCTCTACTAAAAA | 7089 |
rs62125443 | snp | C/G | 0.47802 | 0.102502 | intron-variant | TLE2 | GRCh38.p7 | 19:2999806 | GGGAGGCCAAGGTAG[C/G]CAGATCACCTGAGGT | 7089 |
rs62125444 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3000279 | ACGGGTTTTCACCAT[A/G]TTAGCCAGGGTGGTC | 7089 |
rs62125445 | snp | C/G | 0.304438 | 0.244001 | intron-variant | TLE2 | GRCh38.p7 | 19:3001392 | AGTGCTGGGATTACA[C/G]GTGTGAGCCACTGTG | 7089 |
rs62125446 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3018413 | TTCTCTTGCCTCAGC[C/T]TCCCGAGTAGCTCAG | 7089 |
rs62125450 | snp | C/T | 0.210909 | 0.246925 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048806 | AGGCTTGAACCACCG[C/T]GCCCGGCCTGCTTTT | 7089 |
rs62125451 | snp | A/G | 0.0399052 | 0.1355 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049522 | AGGGTCTCCTGGGCC[A/G]AGGTGAAGAATTTCG | 7089 |
rs66751326 | snp | C/T | 0.367297 | 0.220775 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031288 | ACCTGAACGATGAGG[C/T]TGGGCAGCTCTGGGA | 7089 |
rs66977119 | in-del | -/T | 0.224412 | 0.248687 | intron-variant | TLE2 | GRCh38.p7 | 19:3009885 | CGACTTTCTCTCTCT[-/T]CTTTTTTTCTTTTGT | 7089 |
rs67167576 | in-del | -/TGTTT | 0.155164 | 0.231314 | intron-variant | TLE2 | GRCh38.p7 | 19:3015940 | TTTTGTTCTCTCTTC[-/TGTTT]TGTTTTGTTTTTGAC | 7089 |
rs67282830 | snp | G/T | 0.46875 | 0.121031 | intron-variant | TLE2 | GRCh38.p7 | 19:3009904 | TTTTTTCTTTTGTTT[G/T]AGATGGAATCTTGCT | 7089 |
rs67321857 | in-del | -/C | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3043643 | TCTCTACTAAAAAAA[-/C]AAAAAAAAAAAAAAA | 7089 |
rs67694740 | in-del | -/AT | | | intron-variant | TLE2 | GRCh38.p7 | 19:3006239 | ATTCAGATTGGCCAG[-/AT]AGCCCCACCCCTTTG | 7089 |
rs67980208 | in-del | -/AG | 0.16846 | 0.236329 | intron-variant | TLE2 | GRCh38.p7 | 19:3035918 | TTATTATCCAGAAAC[-/AG]GGGAAAGCGAGTCAC | 7089 |
rs71179947 | in-del | -/T | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:2998293 | TTTTTTTTTTTTTTT[-/T]GTGAGACAGGGTCTA | 7089 |
rs71179948 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030967 | AAAAAAAAAAAAAAA[-/A]GCCCTTATCAAATTT | 7089 |
rs71179949 | in-del | -/CC | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3047517 | TTGTGACCCCCCCCC[-/CC]AGGCATCCTTCTGCT | 7089 |
rs71337191 | in-del | -/A | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3004614 | CAGCAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 7089 |
rs71337195 | in-del | -/T | 0.159622 | 0.233092 | intron-variant | TLE2 | GRCh38.p7 | 19:3033176 | ACCAAGCCTGGCTAA[-/T]TTTTTTTTTTTAATG | 7089 |
rs71337196 | in-del | -/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3043364 | GGCCCCTTCTGCAGC[-/T]TTTTTTTTTTTTTTT | 7089 |
rs71337197 | in-del | -/C/CC | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3047508 | GTGTCGGGCTTGTGA[-/C/CC]CCCCCCCCCAGGCAT | 7089 |
rs71339155 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | TLE2 | GRCh38.p7 | 19:3007054 | CCTCCCGAAGTGCTA[C/G]AATTACAGGCGTGAG | 7089 |
rs71339156 | snp | G/T | 0.334871 | 0.235153 | intron-variant | TLE2 | GRCh38.p7 | 19:3009900 | TTTTTTTTTTCTTTT[G/T]TTTTAGATGGAATCT | 7089 |
rs71339157 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | TLE2 | GRCh38.p7 | 19:3016879 | CGCCTCCCGGGTTCA[C/T]GCCATTCTTCTGCCT | 7089 |
rs71339158 | snp | A/T | 0.0821764 | 0.185298 | intron-variant | TLE2 | GRCh38.p7 | 19:3016900 | TCTTCTGCCTCAGCC[A/T]CCAGAGTAGCTGGGA | 7089 |
rs71339159 | snp | C/T | 0.11228 | 0.208646 | intron-variant | TLE2 | GRCh38.p7 | 19:3025659 | AAGAGGCTGAGCAGA[C/T]GAGAAGGCGTGTGGG | 7089 |
rs71339160 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | TLE2 | GRCh38.p7 | 19:3033456 | ACAGGCGTGAGCCAC[C/T]GCACCCGGCTAATTT | 7089 |
rs71339161 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | TLE2 | GRCh38.p7 | 19:3033799 | CCAAAGAGGCCAGGA[C/G]TTTGAGACCAGCCTG | 7089 |
rs71339244 | in-del | AAAAAAGGA/GAAAAGG | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3010368 | AAACTCCGTCTCAAA[AAAAAAGGA/GAAAAGG]AAAAAAAAAACAAAA | 7089 |
rs72528545 | in-del | -/AA/AT | | | intron-variant | TLE2 | GRCh38.p7 | 19:3006237 | CAATTCAGATTGGCC[-/AA/AT]AGAGCCCCACCCCTT | 7089 |
rs72973268 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TLE2 | GRCh38.p7 | 19:3034168 | CAGAGCATCACCCTA[A/G]CCCTCTATTCCCAAC | 7089 |
rs72973273 | snp | C/T | 0.122064 | 0.214785 | intron-variant | TLE2 | GRCh38.p7 | 19:3041765 | CAATAAATACAGGAA[C/T]GAAAGGCCCGCTGCT | 7089 |
rs72973282 | snp | C/T | 0.156319 | 0.231784 | intron-variant | TLE2 | GRCh38.p7 | 19:3046069 | ATATCTTTGCCTTCC[C/T]AATTAGTCTGGTTGC | 7089 |
rs72973288 | snp | C/G | 0.107694 | 0.205546 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049259 | GGCTGGACTCAGGGT[C/G]TTTGTGTGGGAACTG | 7089 |
rs72988909 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | TLE2 | GRCh38.p7 | 19:3008153 | TTTCAAGTACTGAAA[A/G]CCACGCCCAGCTGGT | 7089 |
rs72988931 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | TLE2 | GRCh38.p7 | 19:3019901 | CCCATTTCTCTTTTA[C/T]CTTTTTCCCTCTCAC | 7089 |
rs72988949 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TLE2 | GRCh38.p7 | 19:3024905 | AAAATGGTCTCTATC[C/T]GTGCTGCAGGCTACG | 7089 |
rs72988950 | snp | G/T | 0.0629771 | 0.165899 | intron-variant | TLE2 | GRCh38.p7 | 19:3025481 | GAGTCCCAGATTCCA[G/T]CCCCGGCTTGGCCCA | 7089 |
rs73516380 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | TLE2 | GRCh38.p7 | 19:3007807 | TAAACATTTTCAGGC[A/C]GGCACAGTGGCTCAC | 7089 |
rs73518037 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | TLE2 | GRCh38.p7 | 19:3036770 | ATACTCCGTGCTGTT[C/G]TGCCTGGGAGCAGCC | 7089 |
rs73919251 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TLE2 | GRCh38.p7 | 19:3009755 | GGACCCAGATCCCGC[C/T]TCCCACTGCCTTGGG | 7089 |
rs73919252 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | TLE2 | GRCh38.p7 | 19:3012760 | TCGGCTTCATGTCAT[C/T]GCCTCCCCTGCCTCC | 7089 |
rs73919260 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | TLE2 | GRCh38.p7 | 19:3027560 | TCCTTGATGGGGATG[C/T]CTGGTGGCCCCTGCC | 7089 |
rs73919261 | snp | C/T | 0.0372196 | 0.131242 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029776 | GTCTCTGCAAAAGGT[C/T]AGGGGTGGTGCGCTA | 7089 |
rs73919264 | snp | A/G | 0.0839998 | 0.186933 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030986 | CTTATCAAATTTAAA[A/G]CCATCGTTTTCCAGC | 7089 |
rs73919266 | snp | A/G | 0.109108 | 0.206518 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031060 | CCAGGCACAGGGATT[A/G]TAAGGGTGGATAAGG | 7089 |
rs73919286 | snp | A/G | 0.109108 | 0.206518 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031172 | ATTTGTACAGACAGA[A/G]GAAGAGTTTAGAGGG | 7089 |
rs74178413 | snp | A/G | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:2998271 | TGTGTGTGTGTGTGT[A/G]TAATTTTTTTTTTTT | 7089 |
rs74182447 | multinucleotide-polymorphism | AAA/TAC | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3043641 | CGTCTCTACTAAAAA[AAA/TAC]AAAAAAAAAAAAAAA | 7089 |
rs74346037 | snp | C/T | 0.0116504 | 0.0754284 | intron-variant, utr-variant-5-prime | TLE2 | GRCh38.p7 | 19:3028914 | GTACATCCTGCCGAT[C/T]CGAAAAGCCCCCCAG | 7089 |
rs74539573 | snp | G/T | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3002717 | TCTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 7089 |
rs74604221 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | TLE2 | GRCh38.p7 | 19:3039669 | CCCCAACACACCACC[A/G]GCTACACTGTATTTA | 7089 |
rs74644429 | snp | C/T | 0.00028182 | 0.0118672 | intron-variant | TLE2 | GRCh38.p7 | 19:3013661 | CAAGGCCCTCCCCTC[C/T]TCCTTACCAGGATGA | 7089 |
rs74688785 | snp | C/G | 0.125528 | 0.21681 | intron-variant | TLE2 | GRCh38.p7 | 19:3021338 | TGAACCCGGGAGTTA[C/G]AGATTGCAGTGAGCC | 7089 |
rs74823704 | snp | G/T | | | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048991 | ACTATTTTTTGGATT[G/T]TTAGTAGAGATAGGG | 7089 |
rs75038561 | snp | G/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3040363 | TTGTTTTTTTTTTAA[G/T]ACAGTCTCGCTCTGT | 7089 |
rs75219197 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049241 | GTGTGTGCCAGCGTG[G/T]CTGGCTGGACTCAGG | 7089 |
rs75348949 | snp | A/C | | | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048988 | CTGACTATTTTTTGG[A/C]TTTTTAGTAGAGATA | 7089 |
rs75476301 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TLE2 | GRCh38.p7 | 19:2998915 | GATCAGCAAACTTCA[C/T]AAAGGGCCTGGTAAA | 7089 |
rs75577928 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE2 | GRCh38.p7 | 19:3020649 | TGCGTGGATTTGTCC[A/G]TTTTCAACTACGTTG | 7089 |
rs75807065 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030885 | AGCCCCAGAAGGTCA[A/C]GGCTGCACTGAGTTG | 7089 |
rs76047628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3015498 | CTTGCATTACAGGAT[C/T]TCCTCTGATTGGTCA | 7089 |
rs76207314 | snp | C/T | 0.000690015 | 0.0185616 | intron-variant | TLE2 | GRCh38.p7 | 19:3006134 | TTTGACCTGCAAACA[C/T]TGCCCCATCTGACTA | 7089 |
rs76302952 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | TLE2 | GRCh38.p7 | 19:3041746 | CTGGCACACAGTAGG[C/T]GCCCAATAAATACAG | 7089 |
rs76393741 | snp | G/T | | | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048989 | TGACTATTTTTTGGA[G/T]TTTTAGTAGAGATAG | 7089 |
rs76731306 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | TLE2 | GRCh38.p7 | 19:3010842 | GTTTCCCTACCCGCC[A/G]AGCTGACACAATGAG | 7089 |
rs76748492 | snp | G/T | 0.149665 | 0.228982 | intron-variant | TLE2 | GRCh38.p7 | 19:3035897 | GGAGGGGGGGCTAAG[G/T]CTCCATTATTATCCA | 7089 |
rs76831712 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TLE2 | GRCh38.p7 | 19:3045920 | AGAGCCTCAGTTTCC[C/T]TATCTGTAAAACAGA | 7089 |
rs76836238 | snp | C/T | 0.0191448 | 0.0959473 | intron-variant | TLE2 | GRCh38.p7 | 19:3015905 | AATGGGAGCTTCCAA[C/T]GGCTGACTCAGTGCT | 7089 |
rs76864144 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TLE2 | GRCh38.p7 | 19:3013173 | AATTTCTAATGCCCT[A/G]GGGGTGCTTTTAGAT | 7089 |
rs77010160 | snp | C/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3011918 | CAAGATTTGCAATTC[C/T]TTTTTTTTTTAATAC | 7089 |
rs77031288 | snp | C/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3023823 | CTTGCACCCAGGAGG[C/T]GGAGGTTGCAGTCAG | 7089 |
rs77189214 | snp | G/T | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3017467 | CTTTTTTTTTTTTTT[G/T]TGAGACAGGGTCTTA | 7089 |
rs77196039 | snp | A/T | 0.0748431 | 0.178382 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997468 | TTAACGATCCTGCCC[A/T]GCGCAACTCCTGTGT | 7089 |
rs77281807 | snp | A/C | 0.0748771 | 0.178415 | intron-variant | TLE2 | GRCh38.p7 | 19:3008991 | GCAGGTGACTCCAAC[A/C]CACCTCTGTGCCACC | 7089 |
rs77292473 | snp | C/T | 6.68952e-05 | 0.005783 | missense | TLE2 | GRCh38.p7 | 19:3002380 | ACTTCAGGGACAGCA[C/T]GCAGCTCTCGTGGAG | 7089 |
rs77298712 | snp | A/G | 0.013075 | 0.0797907 | intron-variant | TLE2 | GRCh38.p7 | 19:3017822 | TATAAAAAGAGTCCC[A/G]GGGTGCCACTCACTT | 7089 |
rs77352760 | snp | C/T | 0.283421 | 0.247756 | intron-variant | TLE2 | GRCh38.p7 | 19:3003142 | AACTGCATGTCGAAT[C/T]ATTAATATTAATCAG | 7089 |
rs77429945 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030592 | AAGGGTTAGGGTTAC[A/T]AAAACCCATTTTGTA | 7089 |
rs77430765 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TLE2 | GRCh38.p7 | 19:3015152 | GAGCCTGCCAGTCTC[C/T]GGGGATCAAGTTGCA | 7089 |
rs77511596 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TLE2 | GRCh38.p7 | 19:3046403 | TTAGCTCCTATTCCC[C/T]GCTCCTTTTCCTCCA | 7089 |
rs77588387 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3021720 | CCCAAGTAGGTGAGA[C/T]TACAGGTGCGCACCA | 7089 |
rs77687605 | snp | C/G | 0.0539704 | 0.155153 | intron-variant | TLE2 | GRCh38.p7 | 19:3025705 | GCATACAATGGCCAC[C/G]GACTTTGCCTCTGCC | 7089 |
rs77862852 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TLE2 | GRCh38.p7 | 19:3032812 | AGTGCTGATTCCAAA[A/C]CCTTTCCGGCAGGTG | 7089 |
rs77892057 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | TLE2 | GRCh38.p7 | 19:3010500 | ACCAGCCCTGACTAT[A/T]CAGGGCTGTGAGTTT | 7089 |
rs78044558 | snp | C/T | | | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048122 | TGTAGTCCCAGCTAC[C/T]TCGGGGGCTGAGGCA | 7089 |
rs78186569 | snp | A/C | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3039977 | CAAATAGCTCGATAG[A/C]TGAAAAGGCCCCGAC | 7089 |
rs78196212 | snp | A/G | 0.040671 | 0.13668 | intron-variant | TLE2 | GRCh38.p7 | 19:3005290 | AGGGGAAGCCTGTGG[A/G]TGTGTCTGGGGGACA | 7089 |
rs78369506 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TLE2 | GRCh38.p7 | 19:3039629 | CATACTATCTGCTCC[C/T]TCCTGTGTGTACGGT | 7089 |
rs78631578 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | TLE2 | GRCh38.p7 | 19:3032571 | TGAGTATGTTTACTC[A/G]GAGGTTGTTCGCGTC | 7089 |
rs78695595 | snp | G/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3043388 | TTTTTTTTTTTTTTT[G/T]AGATGGTCTCGAACG | 7089 |
rs78741016 | snp | A/C | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:2999726 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAGA | 7089 |
rs78913261 | snp | C/T | 0.00269304 | 0.036596 | intron-variant | TLE2 | GRCh38.p7 | 19:3017826 | AAAAGAGTCCCAGGG[C/T]GCCACTCACTTACCC | 7089 |
rs79208160 | snp | G/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3023073 | TTTTTTTTTTTTTTT[G/T]AGACAGAATCTCGCT | 7089 |
rs79280644 | snp | A/C | 0.0766824 | 0.180169 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030672 | GTCATGCCTGTAGCT[A/C]CAGCACTTTGGGAAG | 7089 |
rs79354559 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3017452 | TTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 7089 |
rs79467426 | snp | C/G | 0.0045353 | 0.0474034 | intron-variant | TLE2 | GRCh38.p7 | 19:3009517 | GCCCTGCTGACACCT[C/G]CTGCGCCCCCACCCA | 7089 |
rs79516333 | snp | A/G | 0.444444 | 0.157135 | intron-variant | TLE2 | GRCh38.p7 | 19:3016835 | CCAAGCTGGAGTGCA[A/G]TGGCGCAATCTCGGC | 7089 |
rs79818709 | snp | C/T | 0.0067417 | 0.0576663 | intron-variant | TLE2 | GRCh38.p7 | 19:3013625 | CTGCTTCGGGGCCCC[C/T]GGGATGAATAAAGTG | 7089 |
rs79884873 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE2 | GRCh38.p7 | 19:3001633 | TGGCACTACAGGTGC[A/G]ACCTACTGGCTGTTT | 7089 |
rs79949428 | snp | G/T | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3023072 | TTTTTTTTTTTTTTT[G/T]GAGACAGAATCTCGC | 7089 |
rs80072460 | snp | A/G | 0.0741063 | 0.177655 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029452 | GGAAACTGAGGCCGG[A/G]TGGGGAGGCGCCCAG | 7089 |
rs80127611 | snp | A/G | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3040362 | TTTGTTTTTTTTTTA[A/G]GACAGTCTCGCTCTG | 7089 |
rs80177243 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3007646 | TAGGTTGTGGTGTGG[C/T]GCATGGTAAACAAGC | 7089 |
rs80182883 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TLE2 | GRCh38.p7 | 19:3012940 | TCTCCAATACAACGG[A/G]GCTGACCCATCCCCT | 7089 |
rs80301864 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | TLE2 | GRCh38.p7 | 19:3038333 | CCTGCCTCAGCCTCC[A/G]GAGTAGCTGGAATCA | 7089 |
rs80303210 | snp | A/T | 0.0174313 | 0.0917159 | intron-variant | TLE2 | GRCh38.p7 | 19:3001498 | TGAATGATTTTTTTT[A/T]AAAAAGAGATAGGGT | 7089 |
rs80304995 | snp | A/G | 0.068017 | 0.171412 | intron-variant | TLE2 | GRCh38.p7 | 19:3009735 | GGGACAGGTTTTGAC[A/G]CCCTGGACCCAGATC | 7089 |
rs80318528 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | TLE2 | GRCh38.p7 | 19:3017965 | TAAAGCCCCCCGCCC[C/T]CACCACCCCACTCAG | 7089 |
rs111257087 | snp | C/T | 0.14665 | 0.227637 | intron-variant | TLE2 | GRCh38.p7 | 19:3043340 | ATTATAGGCGTGAGC[C/T]ATGGCACCCGGCCCC | 7089 |
rs111303777 | snp | A/C | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3040155 | GTAACCCCTCTGTAC[A/C]CAGTTGGGGGTTCAC | 7089 |
rs111313851 | snp | C/T | 8.37468e-05 | 0.00647043 | utr-variant-3-prime, synonymous-codon | TLE2 | GRCh38.p7 | 19:2997887 | GGCCTTCTTGTCCCC[C/T]GAGCCTGTCACGATG | 7089 |
rs111335294 | in-del | -/GAG | 0.0599851 | 0.162463 | intron-variant | TLE2 | GRCh38.p7 | 19:3026639 | CTATCTCTGAACCCT[-/GAG]GTCTATCTCAGAACC | 7089 |
rs111363811 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:2999771 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAACA | 7089 |
rs111487699 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | TLE2 | GRCh38.p7 | 19:3011319 | GATCACCTGAGGTCA[C/G]GAGTTCGAGACCAGC | 7089 |
rs111499805 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3002077 | TGTTGGGATGACAGG[C/T]GTGAGCTACCACACC | 7089 |
rs111505545 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TLE2 | GRCh38.p7 | 19:3012019 | GGAGGCCAAGGTGGG[C/T]GGATCACCTGAGATC | 7089 |
rs111708926 | snp | C/T | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3018897 | TGCTGGGATTACAGG[C/T]ATAAGCCACCATGCC | 7089 |
rs111733797 | snp | C/G/T | 3.40681e-05 | 0.00412709 | intron-variant | TLE2 | GRCh38.p7 | 19:3013821 | CTGAGGGTTGGTCCT[C/G/T]GGTTTGAGGAGGTGA | 7089 |
rs111749008 | snp | A/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3026612 | CCTGAGGTCAATCTC[A/T]GAACCCTGAGGTCTA | 7089 |
rs111756954 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3000360 | GATTACAGGCATGAG[C/G/T]GACCGTGCCCGGCTG | 7089 |
rs111915311 | snp | C/G/T | 0.000333127 | 0.0129016 | intron-variant | TLE2 | GRCh38.p7 | 19:3014567 | CTGGACCCCTGGACT[C/G/T]ACCTCGTCCACCACC | 7089 |
rs111958390 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3003072 | TCCAACATTCTCCCT[C/G]TTCAGCACCCCCCTA | 7089 |
rs111973697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3028235 | GACGAGGTTCGGAGT[A/G]GGGCAGGGACCTACC | 7089 |
rs111977781 | snp | A/C | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3000899 | GGTACAATCATAGCT[A/C]ACTGCAGCCTCCACC | 7089 |
rs112011003 | snp | A/G | 0 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:2999740 | TCAAAAAAAAAAAAA[A/G]AAAGAAAAACAGCTG | 7089 |
rs112014346 | snp | A/C/G/T | 2.17417e-05 | 0.00329703 | synonymous-codon | TLE2 | GRCh38.p7 | 19:3011152 | AGGAGTGCTGGCGGG[A/C/G/T]AGGTCATTCTGCAGA | 7089 |
rs112025644 | snp | A/G | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3041172 | GCTGGGATTACAGGT[A/G]CGTGCCACCACGCCT | 7089 |
rs112031948 | snp | A/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3017488 | CAGGGTCTTACTCTG[A/T]CACCCAGGTTGGAGT | 7089 |
rs112087638 | snp | A/G | 0.131723 | 0.220251 | intron-variant | TLE2 | GRCh38.p7 | 19:3044555 | TTCCTGAGTTGCTGG[A/G]ATTACAGGTGTGCGC | 7089 |
rs112089284 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029903 | CTGGGCTCAAGCGAT[C/G]CTTCCCCCTCAGCTT | 7089 |
rs112173780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031236 | ATGTGGGGTGTCTGG[G/T]AGAGGACCCTTGGGG | 7089 |
rs112198595 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3017938 | CGCCAGAGGGTACAG[C/T]CCTCCAGTTTATAAA | 7089 |
rs112201116 | snp | A/G | 0.000116336 | 0.00762591 | synonymous-codon | TLE2 | GRCh38.p7 | 19:3005846 | TGAGGAAGTCAGCTC[A/G]GCCTTGATACGGGGG | 7089 |
rs112219384 | snp | A/G | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3002212 | ATTTGGGATATACTT[A/G]TACTAACGATTTGCT | 7089 |
rs112253682 | snp | A/G | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3024922 | TGCTGCAGGCTACGC[A/G]GCAGAATCAGTGCCT | 7089 |
rs112268932 | in-del | -/A | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3044171 | AGACTCCGTCTCACC[-/A]AAAAAAAAAAACAAA | 7089 |
rs112292499 | snp | A/G | 0.435263 | 0.167862 | intron-variant | TLE2 | GRCh38.p7 | 19:3032118 | TTTGTATTATTAGTA[A/G]AGACGGATTCACCAT | 7089 |
rs112318973 | in-del | -/AAAC | 0.35574 | 0.226537 | intron-variant | TLE2 | GRCh38.p7 | 19:3012261 | CATCTCCAAAACGAA[-/AAAC]AAACAAACAAAAGGC | 7089 |
rs112319958 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3040312 | AACAAACCCCTGGCC[G/T]CATGGCCCAATCTGA | 7089 |
rs112345934 | snp | G/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3037195 | GAGACTGAGGCAGGA[G/T]AATTGCTTGAACCTG | 7089 |
rs112346473 | snp | C/T | 0 | 0 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049346 | CTTCAGAAAAGTGAC[C/T]TCTAGGGAGTCTCAG | 7089 |
rs112389572 | snp | A/C/G | 0.158302 | 0.232576 | intron-variant | TLE2 | GRCh38.p7 | 19:3043413 | CGAACGCCTAACCTC[A/C/G]TGATCCGCCCGCTTC | 7089 |
rs112399902 | snp | C/T | 0.363359 | 0.222822 | intron-variant | TLE2 | GRCh38.p7 | 19:3032104 | CCCAGCTAATTTTTT[C/T]TGTATTATTAGTAGA | 7089 |
rs112430601 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TLE2 | GRCh38.p7 | 19:3033414 | CCTCGTGATCCGCCC[A/G]CCTCAGCCTCCCAAA | 7089 |
rs112453611 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3018232 | GAGTTCCCGGGCTCA[A/G]GTGATTGTCCCATCT | 7089 |
rs112501424 | snp | C/T | 0.081446 | 0.184634 | intron-variant | TLE2 | GRCh38.p7 | 19:3045629 | CGAGACCAGCCTGGC[C/T]AACATGGTGAAACCA | 7089 |
rs112527548 | snp | A/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3047194 | CCCGTCCTCCGCCTC[A/T]TTAGGCGCGGCCGCG | 7089 |
rs112579334 | in-del | -/G | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3005276 | CTTTAGAGAGTTACA[-/G]GGGAAGCCTGTGGAT | 7089 |
rs112713447 | snp | A/G | 0.5 | 0 | synonymous-codon | TLE2 | GRCh38.p7 | 19:3006618 | CAGTGCATCCGAGGG[A/G]AAGGGAACCGGCTGC | 7089 |
rs112744806 | snp | C/T | 0.357024 | 0.225933 | intron-variant | TLE2 | GRCh38.p7 | 19:3024079 | CTGCTCACTGCAACC[C/T]CCGCCTCCTGAGTTC | 7089 |
rs112773445 | snp | A/C | | | intron-variant | TLE2 | GRCh38.p7 | 19:3016321 | TGGCTCACGCCTATA[A/C]TCCCAGCACTTTGGG | 7089 |
rs112798879 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | TLE2 | GRCh38.p7 | 19:3021771 | TACTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 7089 |
rs112802039 | snp | A/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3026606 | CTGAACCCTGAGGTC[A/T]ATCTCAGAACCCTGA | 7089 |
rs112804466 | snp | A/C | 0.0955749 | 0.196603 | intron-variant | TLE2 | GRCh38.p7 | 19:3026228 | GAGGCAGGTGGATCA[A/C]CTGAGGTCAGGAGTT | 7089 |
rs112835409 | snp | C/T | 0.040671 | 0.13668 | intron-variant | TLE2 | GRCh38.p7 | 19:3028213 | TGCCCAATGTACAGA[C/T]GGGGAAGACGAGGTT | 7089 |
rs112863154 | in-del | -/A | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3004615 | CAGCAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 7089 |
rs112961044 | snp | C/G | 0.0988009 | 0.199095 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048087 | ATACAAAAAATTAGC[C/G]AGGTGTGGTGGCGGG | 7089 |
rs113000631 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029215 | GCGCGCCGCGGCCGG[A/G]TTTCGGTGGCGGCGG | 7089 |
rs113088160 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3004605 | GATCACAACACAGCA[A/G]CTCTGTCTCAAAAAA | 7089 |
rs113163348 | snp | A/T | 0 | 0 | splice-donor-variant | TLE2 | GRCh38.p7 | 19:3014568 | TGGACCCCTGGACTC[A/T]CCTCGTCCACCACCA | 7089 |
rs113170939 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3035884 | GACCGGATTGGAGGA[-/G]GGGGGGGCTAAGGCT | 7089 |
rs113204121 | snp | A/G | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3004739 | CAATTACAGAAAGAA[A/G]AGAAAGGCATTTCAG | 7089 |
rs113230205 | snp | C/T | 0.029116 | 0.117091 | intron-variant | TLE2 | GRCh38.p7 | 19:3017297 | CACCCGCCGCCACGT[C/T]TGGCTAATTTTTGAA | 7089 |
rs113255406 | snp | G/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3034678 | CTCCTGTCTTCTCCA[G/T]ACGCGCGTACACACA | 7089 |
rs113268472 | snp | A/G | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3000559 | CGGGGGGACCTGGGG[A/G]ACAGGGACAGGGGCA | 7089 |
rs113276374 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049409 | GAACCCTGTTCCAGG[C/G]AGAGGGAACAGCATG | 7089 |
rs113352342 | in-del | -/TCT | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3023054 | AGTCATTTTACCTAA[-/TCT]TCTTTTTTTTTTTTT | 7089 |
rs113353995 | in-del | -/TT | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3002703 | TCACGCTGGATAATC[-/TT]TTTTTTTTTTTTTGA | 7089 |
rs113398377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3006352 | CCAGCCTGCGAACAC[C/T]GCCCCATTGGAACAT | 7089 |
rs113541352 | snp | A/T | 0.264906 | 0.249555 | intron-variant | TLE2 | GRCh38.p7 | 19:3020116 | GGTGAAACACCTGTA[A/T]TCCCAGCTACTCAGG | 7089 |
rs113546989 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3026213 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 7089 |
rs113549717 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TLE2 | GRCh38.p7 | 19:3027168 | AGGTCTATTTCAGAA[A/C]CCTGAAGTCTGTCTC | 7089 |
rs113553089 | snp | C/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:2998032 | TGGGCAAGGCTGGGG[C/T]GGAGTCAGGAACGGG | 7089 |
rs113566576 | snp | C/T | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3010585 | CCAAGGCCAGCTTCT[C/T]TCAGGGGCCCCAGAA | 7089 |
rs113620466 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3026363 | TGAGGCAGGAGAGGC[A/G]CTTGCACTCAGGAGG | 7089 |
rs113634003 | snp | A/G | 0 | 0 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048132 | GCTACCTCGGGGGCT[A/G]AGGCAGGAGAATCAC | 7089 |
rs113666435 | snp | C/T | 0.135484 | 0.22223 | intron-variant | TLE2 | GRCh38.p7 | 19:3043423 | ACCTCGTGATCCGCC[C/T]GCTTCAGCCTCCCAA | 7089 |
rs113701187 | snp | A/C | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3034677 | CCTCCTGTCTTCTCC[A/C]TACGCGCGTACACAC | 7089 |
rs113721439 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | TLE2 | GRCh38.p7 | 19:3012314 | TCAACCTCCCATGCT[C/T]GAGTGATCCTCCCGA | 7089 |
rs113734238 | in-del | -/T | 0.129664 | 0.219133 | intron-variant | TLE2 | GRCh38.p7 | 19:3024167 | ACCATGCCCGGCTAA[-/T]TTTTTTTTTTTAAGT | 7089 |
rs113834616 | snp | A/G | 0.5 | 0 | intron-variant | TLE2 | GRCh38.p7 | 19:3033981 | CAGGCTTCAGTGACC[A/G]CCTCGTGAGGATGGC | 7089 |
rs113869697 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3008859 | CAGGGAGCCCCACCC[C/T]GGTACTCACGGCTTT | 7089 |
rs113870140 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | TLE2 | GRCh38.p7 | 19:3038083 | GCTGAGATCACACCA[C/G]TGCACTCCAGCCTGG | 7089 |
rs113920090 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | TLE2 | GRCh38.p7 | 19:3025191 | AGGGTTGGGGAGGTG[A/G]CGCCCGCAGGTGCAC | 7089 |
rs113955961 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | TLE2 | GRCh38.p7 | 19:3047260 | CGCCCGCGGCGCAGT[C/T]GTTAAGCGCGGGGCG | 7089 |
rs114136854 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | TLE2 | GRCh38.p7 | 19:3009336 | CTTAATCGCTGTTGC[A/G]TTTTTCCACAATCAG | 7089 |
rs114201443 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TLE2 | GRCh38.p7 | 19:2998899 | AATGGCTTAGACCAG[A/G]GATCAGCAAACTTCA | 7089 |
rs114257572 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | TLE2 | GRCh38.p7 | 19:3022109 | GCTGGAATGCAGTGG[C/T]GTGATCTCGGTTCAC | 7089 |
rs114293261 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | TLE2 | GRCh38.p7 | 19:3037490 | CCCCTAGCTTTGCTG[A/T]GTGGATCTGGGAACA | 7089 |
rs114320132 | snp | A/G | 0.137187 | 0.223099 | intron-variant | TLE2 | GRCh38.p7 | 19:2999277 | ACAGAGAAGGACTCC[A/G]TGTCAAAAAAACAAA | 7089 |
rs114410522 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TLE2 | GRCh38.p7 | 19:3014868 | ACTACATGAGTGCCC[C/T]GTGTGACTCCCGGCC | 7089 |
rs114676805 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | TLE2 | GRCh38.p7 | 19:3024382 | GGTTGTGCAGCCATC[A/C]CCAGCACCATCTCCA | 7089 |
rs114688229 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TLE2 | GRCh38.p7 | 19:2998105 | GATGGAGTTTTGTTC[C/T]TGTCGCCCAGGCTGA | 7089 |
rs114823615 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | TLE2 | GRCh38.p7 | 19:3026104 | AAACCACTGGCCAGT[C/T]TCAGGATCTCAGGAT | 7089 |
rs114826332 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TLE2 | GRCh38.p7 | 19:3008069 | CCTGGGGGACAGAGC[A/G]AAACTCAGTCTCAGA | 7089 |
rs114834690 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TLE2 | GRCh38.p7 | 19:3040708 | GCTGGAGTGCAGTGA[C/T]ATGATCACGGCTCCC | 7089 |
rs114863786 | snp | C/G | 0.483636 | 0.0889627 | intron-variant | TLE2 | GRCh38.p7 | 19:3046932 | TCCTCCCCCTCCTCT[C/G]CCTCCCCCTCCTCCT | 7089 |
rs114935319 | snp | A/C/G | 0.110167 | 0.207236 | intron-variant | TLE2 | GRCh38.p7 | 19:3009011 | TCTGTGCCACCCCAC[A/C/G]CCCACCTGCCATACC | 7089 |
rs115032880 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3015440 | TGGGAAAATGGCTGT[A/G]CGGCCAAGAGGCCGC | 7089 |
rs115052612 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049309 | CCCACCCTGCTTTTG[A/G]TGGGTGAGAGTCAGA | 7089 |
rs115078972 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | TLE2 | GRCh38.p7 | 19:3013020 | GCCCCAACCTCTGGC[A/G]GTTGCCATGGTAACC | 7089 |
rs115092746 | snp | A/G | 0.151668 | 0.229849 | intron-variant | TLE2 | GRCh38.p7 | 19:3012240 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTCCAA | 7089 |
rs115178636 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE2 | GRCh38.p7 | 19:3035935 | GGGAAAGCGAGTCAC[C/T]CCCAAGCCTGGCCTA | 7089 |
rs115387851 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | TLE2 | GRCh38.p7 | 19:3038300 | GCAGCCTTGACCTCG[C/T]TGGGCTCAAGCCGTC | 7089 |
rs115401915 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TLE2 | GRCh38.p7 | 19:3008439 | TAGCTTATGCAAGAG[A/G]CTTTTTTTCTTTTTT | 7089 |
rs115416951 | snp | C/G | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030377 | AGGCCCACCCGGGGA[C/G]TGGGAAGTTCTTATT | 7089 |
rs115640086 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049197 | AAGTGATTCTCCAAT[C/T]TCAGCCTCCCAAAGT | 7089 |
rs115646716 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3035709 | GTCAGTGACGTCACA[C/T]AGGAAACTGGCCAAT | 7089 |
rs115815855 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TLE2 | GRCh38.p7 | 19:3010061 | TTGGCAAACTCCTAT[C/T]CATCCTTCAAAACCC | 7089 |
rs115991724 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TLE2 | GRCh38.p7 | 19:3013948 | CCATGGGAAGATTAT[A/G]AAATCTTCTGCTGCC | 7089 |
rs116119979 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TLE2 | GRCh38.p7 | 19:3025806 | ATCCCAGGGTGTCCC[A/G]CACCCCATAAAGGGG | 7089 |
rs116227649 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE2 | GRCh38.p7 | 19:3037979 | ATAGAAAAATTAGTC[A/G]AGCAAGGTGGCACAC | 7089 |
rs116277347 | snp | C/T | 0.155325 | 0.23138 | intron-variant | TLE2 | GRCh38.p7 | 19:3033812 | GAGTTTGAGACCAGC[C/T]TGGGCAACATAGCGA | 7089 |
rs116278279 | snp | C/G | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030078 | AAAGTGCTGGGATTA[C/G]GGGCGGGAGCCACCG | 7089 |
rs116340452 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TLE2 | GRCh38.p7 | 19:3009340 | ATCGCTGTTGCGTTT[C/T]TCCACAATCAGAAGT | 7089 |
rs116372368 | snp | C/T | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030909 | TGAGTTGAGATCACA[C/T]CACTGCACTCCAGCC | 7089 |
rs116376481 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | TLE2 | GRCh38.p7 | 19:3026650 | ACCCTGTCTATCTCA[A/G]AACCCTGAGGTCTAT | 7089 |
rs116496125 | snp | C/T | 0.0418186 | 0.138422 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030558 | GTGTCCTTAGGTGAT[C/T]GAGTACCTAATGGTA | 7089 |
rs116529982 | snp | A/G | 0.00183996 | 0.0302753 | intron-variant | TLE2 | GRCh38.p7 | 19:3006149 | CTGCCCCATCTGACT[A/G]TAAGCTCCATCCTTT | 7089 |
rs116592541 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TLE2 | GRCh38.p7 | 19:3031710 | CCTCACACCAGGCAC[A/G]GTCCAGCCTCAGGGC | 7089 |
rs116688482 | snp | C/T | 0.039522 | 0.134904 | intron-variant | TLE2 | GRCh38.p7 | 19:3018085 | CTCAAGACACACAGC[C/T]CATTGGGGGTGATGT | 7089 |
rs116772014 | snp | A/C/G | 0.030278 | 0.119257 | intron-variant | TLE2 | GRCh38.p7 | 19:3001613 | GCCTCAGCCTCCCTC[A/C/G]TACCTGGCACTACAG | 7089 |
rs116833047 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TLE2 | GRCh38.p7 | 19:3045506 | GAGTCCAGAAACTTC[C/T]TTCTCTTAAACCAAA | 7089 |
rs116837122 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TLE2 | GRCh38.p7 | 19:3015578 | TGGCCAGAGCTGGGC[C/T]CTGGAAGGCTCTGAG | 7089 |
rs116854318 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:2999331 | GGCATATTAAAAACA[C/G]TGTACCAACCAGGAC | 7089 |
rs116997560 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | TLE2 | GRCh38.p7 | 19:3004255 | ACCATGGGATCCCTA[C/G]AAATGTTCTTAGCCC | 7089 |
rs117008739 | snp | A/G | 0.0776822 | 0.181126 | intron-variant, synonymous-codon | TLE2 | GRCh38.p7 | 19:3000665 | GAAAATGCTGGCCCC[A/G]TACGGCGTCCTCCAG | 7089 |
rs117117014 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | TLE2 | GRCh38.p7 | 19:3028574 | CCCTCTGCACCTGCG[C/T]TTCCACCTGGAGGCC | 7089 |
rs117181753 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | TLE2 | GRCh38.p7 | 19:3009772 | CCCACTGCCTTGGGA[A/G]CTCCCTGGCCTTTCA | 7089 |
rs117298441 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TLE2 | GRCh38.p7 | 19:3043258 | GTAGCTGAGACCACA[A/G]TCGTACACTACCATG | 7089 |
rs117401653 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TLE2 | GRCh38.p7 | 19:3026921 | AACCCTGAGGTCTAT[C/T]TCAGGACCTTGAGGT | 7089 |
rs117415317 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | TLE2 | GRCh38.p7 | 19:3014677 | CCACACCCCCTATCC[A/G]CTCCTCAGGAGTTGG | 7089 |
rs117510975 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | TLE2 | GRCh38.p7 | 19:3020008 | ACAAATCAGGCCGGG[C/T]ATGGTGGCTCACGCC | 7089 |
rs117643833 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TLE2 | GRCh38.p7 | 19:3041866 | AGAGAGGCCTAGGGA[C/T]CTGCCCACGGTCACA | 7089 |
rs117709111 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3023966 | TACTGAGGATGAAAG[C/G]AACCTGGGGCACTCT | 7089 |
rs117841011 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030158 | TCCCTACACAGAGCA[A/G]ACTTCCACAGATGGG | 7089 |
rs117962813 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TLE2 | GRCh38.p7 | 19:3005147 | ACCACCCAGCTACAC[A/G]AGGAAAGGCACATAT | 7089 |
rs118030930 | snp | C/T | 0.0525514 | 0.153343 | missense | TLE2 | GRCh38.p7 | 19:3011148 | AGGCAGGAGTGCTGG[C/T]GGGAAGGTCATTCTG | 7089 |
rs118047726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3002855 | AGGTACCTGCTAGTA[C/T]GCCCGGGTAATTTTT | 7089 |
rs118081031 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | TLE2 | GRCh38.p7 | 19:3011952 | GTCTTGCTCTCAAAA[C/G]TAACATGATCAGACA | 7089 |
rs118107613 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TLE2 | GRCh38.p7 | 19:3020644 | AAACCTGCGTGGATT[C/T]GTCCGTTTTCAACTA | 7089 |
rs118111524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3032786 | GATTCCAGGTTCTTG[A/G]GGGTCTGTGAAGTGC | 7089 |
rs118133572 | snp | C/T | 0.040671 | 0.13668 | intron-variant | TLE2 | GRCh38.p7 | 19:3003995 | TACAGGCGTGAGCCA[C/T]TGCACCCGGCCTCGG | 7089 |
rs137939250 | snp | A/G | | | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049599 | TTTTTTTTTTTTTGA[A/G]ACAGAATCTCACTCT | 7089 |
rs137951030 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3021932 | GATTTCAGGTCGGGC[A/G/T]CAGTGGCTCATGCCT | 7089 |
rs138000508 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE2 | GRCh38.p7 | 19:3008504 | TGCCCAGGCTGGAGT[A/G]CAATGGCACGGTCTC | 7089 |
rs138004716 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE2 | GRCh38.p7 | 19:3046331 | CTCAGCTGCAGACAA[C/T]TCAGCCAGCGCAGGC | 7089 |
rs138060317 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TLE2 | GRCh38.p7 | 19:3017607 | AGGCATGGACCACCA[C/T]ACCCAGCCAACTTTT | 7089 |
rs138060894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3034884 | CGTACCCTCCCAGGG[C/T]CACATAGGGTCAGTG | 7089 |
rs138071704 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TLE2 | GRCh38.p7 | 19:3043547 | TCGCACCTGTAATCC[C/T]GGCAGTTTGGGAGGC | 7089 |
rs138187206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030327 | AAAGGCTCCAGCCCC[A/G]ACCAGAGACCACAGA | 7089 |
rs138270322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3004330 | ACTCCTGAAAGAGAA[A/G]AGCAGGTTGGACATA | 7089 |
rs138298409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:2998573 | ATGAGCCACCGCACC[C/T]GGCCTAATTTTTGTA | 7089 |
rs138332629 | in-del | -/TGTGTGT | | | intron-variant | TLE2 | GRCh38.p7 | 19:2998244 | CCCGGCCAATGTGTG[-/TGTGTGT]GTGTGTGTGTGTGTG | 7089 |
rs138456025 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | TLE2 | GRCh38.p7 | 19:3025902 | CAGAACCAACAGAAC[A/C]CCCACACATGCAGGA | 7089 |
rs138476864 | snp | A/C | | | intron-variant | TLE2 | GRCh38.p7 | 19:3044033 | CAAAAGGTAGCCAGG[A/C]GTGGTGGTGCATCCC | 7089 |
rs138624472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3004700 | GCAAATGAGATGGGT[C/T]TTGAGGGATGAATAG | 7089 |
rs138636484 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3017920 | AGGCGTTTGTATCCA[C/T]GGCGCCAGAGGGTAC | 7089 |
rs138691375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3014986 | TTAATAAATAAATAA[A/G]TAAAATTCATTGCCA | 7089 |
rs138712896 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TLE2 | GRCh38.p7 | 19:3010614 | AACCAGCCCAGGGCC[C/T]GACCATAAGGCAGAA | 7089 |
rs138762400 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TLE2 | GRCh38.p7 | 19:3000073 | ATGGCAAATTTTATT[G/T]TTATTTATTTATTTT | 7089 |
rs138945358 | in-del | -/AC | 0.122411 | 0.214991 | intron-variant | TLE2 | GRCh38.p7 | 19:3034686 | ACGCGCGTACACACA[-/AC]CACACACACATACAC | 7089 |
rs138948303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029848 | GTTGCCCAGGCTGGA[A/G]TACAGTGGGGCAATC | 7089 |
rs139103406 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TLE2 | GRCh38.p7 | 19:3011247 | CTGGGGTTGGGGGCG[A/G]CCAGTCGCAGTGTCT | 7089 |
rs139108329 | in-del | -/AAAAGAAAAGA | | | intron-variant | TLE2 | GRCh38.p7 | 19:3023908 | CACACACACACACAC[-/AAAAGAAAAGA]AAAAGAAAAAAGAAA | 7089 |
rs139149249 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | TLE2 | GRCh38.p7 | 19:3039387 | CCTCCCACTTCTCCC[A/C]CTCTGTTCCAGCCAC | 7089 |
rs139164384 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3033901 | CCTTCCTTAGCCCGG[A/T]CACTTGAATGTCAAC | 7089 |
rs139220911 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | TLE2 | GRCh38.p7 | 19:3036946 | GGATTTAGCGCCCCC[A/G]TTGGGAAGTTGGGAT | 7089 |
rs139272648 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3023667 | GGAGCCTGACACGGG[C/T]GGATTGCTTGAGTCC | 7089 |
rs139348419 | snp | C/T | 0.0137849 | 0.0818684 | intron-variant | TLE2 | GRCh38.p7 | 19:3005413 | TAGAGCTTCCATCCC[C/T]CTCCTGCCAGAACCG | 7089 |
rs139375491 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | TLE2 | GRCh38.p7 | 19:3018586 | GCGTGAACCACCGTG[A/C]CTGGCTATCTATTTT | 7089 |
rs139691786 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3027070 | GTCAATCTCAGAACC[A/G]TGAGGTCTATCTCAG | 7089 |
rs139715743 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TLE2 | GRCh38.p7 | 19:2999047 | GGCGCTTCCGGAGGC[C/T]GAGGCAGGTGGATCA | 7089 |
rs139873710 | snp | A/G | 0.00129225 | 0.0253861 | intron-variant | TLE2 | GRCh38.p7 | 19:3006158 | CTGACTATAAGCTCC[A/G]TCCTTTACCTATAAG | 7089 |
rs140009597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3015965 | TGTTTTTGACGGAGT[C/T]TTGCTCTGCTGCCCA | 7089 |
rs140084584 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE2 | GRCh38.p7 | 19:3019539 | GCCCAAGAGGTAGAC[A/G]CAGGGGATGGGACCT | 7089 |
rs140110426 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3044833 | AGACAAACTCTCTTC[A/G]CCAAAGTCATATTAG | 7089 |
rs140119196 | snp | A/G | 0.0107246 | 0.0724382 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997628 | CCGGTTCCCCAGCCC[A/G]AGAGAGAAGTGCGGA | 7089 |
rs140142996 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | TLE2 | GRCh38.p7 | 19:3011353 | GCCAACATGGTAAAA[C/T]CCCATCTCTACTAAA | 7089 |
rs140204257 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3009395 | ACTACTGAGACCCCC[A/C]GATTGTCTTCCCATG | 7089 |
rs140210230 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049408 | AGAACCCTGTTCCAG[A/G]CAGAGGGAACAGCAT | 7089 |
rs140250593 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TLE2 | GRCh38.p7 | 19:3032523 | GATTACAGGCTTGAG[A/C]CACCGTGCCCAGCCC | 7089 |
rs140295801 | in-del | -/GA | | | intron-variant | TLE2 | GRCh38.p7 | 19:3010375 | GTCTCAAAAAAAAAG[-/GA]AAAAAAAAAACAAAA | 7089 |
rs140358649 | in-del | -/TGTG | | | intron-variant | TLE2 | GRCh38.p7 | 19:2998238 | ACCACGCCCGGCCAA[-/TGTG]TGTGTGTGTGTGTGT | 7089 |
rs140408991 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TLE2 | GRCh38.p7 | 19:3042967 | CGGTTTCAGCTCCCT[C/T]CTCTAGTTTTTAATT | 7089 |
rs140507052 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TLE2 | GRCh38.p7 | 19:3012328 | TCGAGTGATCCTCCC[A/G]ACTGAGCCTCCCAAG | 7089 |
rs140537535 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029994 | CAGAGATGGAGTAGG[G/T]GGGCGTCTCACTATG | 7089 |
rs140562413 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TLE2 | GRCh38.p7 | 19:3026857 | TCAGAACCTTGAGGT[A/C]TATCTCAGAACTCTG | 7089 |
rs140675876 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3024904 | GAAAATGGTCTCTAT[C/G]CGTGCTGCAGGCTAC | 7089 |
rs140715805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:2999772 | GCGCAGTGGCTCACG[C/T]CTGTAATCCCAACAC | 7089 |
rs140844301 | in-del | -/CA | 0.317221 | 0.248005 | intron-variant | TLE2 | GRCh38.p7 | 19:3023888 | AGAGCAAGAATCCAT[-/CA]CACACACACACACAC | 7089 |
rs140971734 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | TLE2 | GRCh38.p7 | 19:3047443 | CGGATCGCAGGCCAG[A/G]CCGTGGCTGAGTAGG | 7089 |
rs140985614 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3033623 | TCTTCTGCCTAAGCC[C/T]CTGGCTCTGGAAACC | 7089 |
rs141016146 | snp | C/G | 0.0707826 | 0.174302 | intron-variant | TLE2 | GRCh38.p7 | 19:3044508 | CACTGCACCCTCCAC[C/G]TCCCGGGTTCAAGTG | 7089 |
rs141028943 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | TLE2 | GRCh38.p7 | 19:2999987 | GCAGTGAGCCGAGAT[C/T]GCAACACTGCACTCC | 7089 |
rs141030577 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | TLE2 | GRCh38.p7 | 19:3040128 | GCAGCAACCCCATCA[A/C]CCACACCACGTGTAA | 7089 |
rs141103605 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TLE2 | GRCh38.p7 | 19:3013551 | ACAGGGAAAGGGTGG[A/G]CAATGCCAGCCCGGC | 7089 |
rs141194377 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3010745 | CTGGTCTGAAACCCA[A/C]GTCTGTCTGGCCCCA | 7089 |
rs141244700 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE2 | GRCh38.p7 | 19:3017258 | TTCTCCTGCCTTGAC[C/T]TCCCGAGTAGCTGGG | 7089 |
rs141341121 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE2 | GRCh38.p7 | 19:3008321 | CTCCAGGCCAGGAAC[A/G]TCTCCTCCCCCAGCT | 7089 |
rs141506338 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3031996 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCTGCAA | 7089 |
rs141615882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3036772 | ACTCCGTGCTGTTCT[A/G]CCTGGGAGCAGCCAG | 7089 |
rs141685515 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE2 | GRCh38.p7 | 19:3014433 | TCCCGGAGTCCCTGA[C/T]GCTTCCTGACCCCAT | 7089 |
rs141711168 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TLE2 | GRCh38.p7 | 19:3038766 | TACAAAAATTAAGGC[C/T]GGGCGCAGTGGCTCA | 7089 |
rs141777928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3038148 | AATAACAATAACAAT[A/G]ATAATAATGCATAGT | 7089 |
rs142034755 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | TLE2 | GRCh38.p7 | 19:3028199 | CTGAAATCCCAACCT[C/G]CCCAATGTACAGACG | 7089 |
rs142056532 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TLE2 | GRCh38.p7 | 19:3017624 | CCCAGCCAACTTTTT[A/G]TATTTTTCTGTAGAG | 7089 |
rs142072423 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE2 | GRCh38.p7 | 19:3039922 | GTGATCCTGTACAGT[A/G]GGATAATTATAGAAA | 7089 |
rs142253716 | snp | G/T | 0.124837 | 0.216412 | intron-variant | TLE2 | GRCh38.p7 | 19:2998292 | AATTTTTTTTTTTTT[G/T]TGTGAGACAGGGTCT | 7089 |
rs142281947 | in-del | -/TGTGTG | | | intron-variant | TLE2 | GRCh38.p7 | 19:2998238 | ACCACGCCCGGCCAA[-/TGTGTG]TGTGTGTGTGTGTGT | 7089 |
rs142432613 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE2 | GRCh38.p7 | 19:3009805 | TAGAGTTTCCATGTG[C/T]TGGTTCCACATTGGC | 7089 |
rs142441905 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | TLE2 | GRCh38.p7 | 19:3043845 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGGGCCT | 7089 |
rs142444584 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | TLE2 | GRCh38.p7 | 19:3009083 | TTCTCTCTGCCTGTC[A/C]CACTACAGATGAGAG | 7089 |
rs142446093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3007642 | AGTCTAGGTTGTGGT[A/G]TGGCGCATGGTAAAC | 7089 |
rs142505650 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE2 | GRCh38.p7 | 19:3039462 | CCTCTGCACTGCATT[A/G]GTTGTTCCCTCTGCC | 7089 |
rs142531594 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3008570 | ATTCTCCTGCCTCAG[A/C]CTCCCGAGTAGCTGG | 7089 |
rs142550881 | in-del | -/A | 0.0252325 | 0.109451 | intron-variant | TLE2 | GRCh38.p7 | 19:3024665 | CAACTTCACACCTAC[-/A]GCTACTGAAAAAACA | 7089 |
rs142682765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3017924 | GTTTGTATCCACGGC[A/G]CCAGAGGGTACAGCC | 7089 |
rs142737706 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | TLE2 | GRCh38.p7 | 19:3020616 | TAATTCTGCCTCCTA[C/T]GATCGCCTTCCTAAA | 7089 |
rs142834962 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TLE2 | GRCh38.p7 | 19:3018742 | GCCTCAGCCTCCCGA[C/G]TAGCTGAGATTACAG | 7089 |
rs142842415 | in-del | -/GC | 0.422315 | 0.181128 | intron-variant | TLE2 | GRCh38.p7 | 19:2998484 | GGTTTCACCATGTTG[-/GC]CAGGTTGGGCTTGAA | 7089 |
rs142867678 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031076 | TAAGGGTGGATAAGG[A/G]AGACAGATCCCTGCC | 7089 |
rs142919980 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | TLE2 | GRCh38.p7 | 19:3023099 | TCGCTGTGTTGCCCA[A/G]GCTGGAGTGCAATGG | 7089 |
rs142935933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3045029 | TTCAGACCAGCCTGG[C/T]CAACATGGCAAGACC | 7089 |
rs142962943 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3034316 | TTTGGTGATCTTCAA[C/T]TGGAGCCTGGCCCTC | 7089 |
rs143101765 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997551 | GAATTCTCGTTACGT[A/C]TGACCCCATCCCCAG | 7089 |
rs143136162 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3047720 | CAAGTAAATATGTTG[G/T]CATTCCTGCAGTTCT | 7089 |
rs143213071 | in-del | -/TTTG | | | intron-variant | TLE2 | GRCh38.p7 | 19:3001436 | GTGCCCAGCCCAAGT[-/TTTG]TTTGTTTGTTTGTTT | 7089 |
rs143214256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3007798 | GAAATTAAATAAACA[C/T]TTTCAGGCCGGCACA | 7089 |
rs143247548 | snp | G/T | 0.031825 | 0.122064 | intron-variant | TLE2 | GRCh38.p7 | 19:3041317 | CAGGAGTGAGCCCCC[G/T]CGCCCAGCCTGCCAT | 7089 |
rs143292043 | snp | A/G | 0.0232847 | 0.105357 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049195 | TCAAGTGATTCTCCA[A/G]TCTCAGCCTCCCAAA | 7089 |
rs143317028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3003000 | CACCATGTCAGCCTA[C/T]GAGCCCCTTTGGATA | 7089 |
rs143542385 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3019552 | ACACAGGGGATGGGA[C/T]CTAAGCACAGCATGT | 7089 |
rs143557528 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TLE2 | GRCh38.p7 | 19:3014015 | TTTGAGTCTCGCTCC[A/G]TTACCCAGGCTGGAG | 7089 |
rs143617265 | in-del | -/TCT | | | intron-variant | TLE2 | GRCh38.p7 | 19:3023055 | GTCATTTTACCTAAT[-/TCT]CTTTTTTTTTTTTTT | 7089 |
rs143667795 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3010235 | TGGGCATGGTGGTGC[A/C]TGCCCGTAATTCCAG | 7089 |
rs143708978 | in-del | -/ATA | | | intron-variant | TLE2 | GRCh38.p7 | 19:3041011 | TATATATATATATAT[-/ATA]TTTTTTTTTTTTTTT | 7089 |
rs143713547 | snp | C/T | 0.0232044 | 0.105184 | intron-variant, missense | TLE2 | GRCh38.p7 | 19:3000657 | AGTACCTGGAAAATG[C/T]TGGCCCCGTACGGCG | 7089 |
rs143765943 | in-del | -/TGTGTGTGTGTGTGTGTGTGTGTG | | | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031343 | GGATAAAGATACAAT[-/TGTGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 7089 |
rs143803986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3004474 | GAAACCCTGTCTCTA[C/T]CGACAAATACAAAAA | 7089 |
rs143868676 | snp | A/G | 0.021333 | 0.101051 | intron-variant | TLE2 | GRCh38.p7 | 19:3039599 | GTCTTCCGAGGCCTC[A/G]TGGCTCTGGGAACAC | 7089 |
rs143963577 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TLE2 | GRCh38.p7 | 19:3037128 | GGTCTTTACTAAAAA[C/T]ACAAAAATTAGCCGG | 7089 |
rs144002073 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3033099 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 7089 |
rs144026138 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3035196 | AGCAGCGGGTGGAAT[C/T]TGGGGAGACTCTGCT | 7089 |
rs144033921 | snp | C/T | 0.0117077 | 0.0756095 | intron-variant | TLE2 | GRCh38.p7 | 19:3005427 | CCCTCCTGCCAGAAC[C/T]GAACAGCACCTGGGA | 7089 |
rs144068393 | in-del | -/GAACCCTGAGGTCAATCTCA | | | intron-variant | TLE2 | GRCh38.p7 | 19:3026593 | CTGAGGTCTATCTCT[-/GAACCCTGAGGTCAATCTCA]GAACCCTGAGGTCTA | 7089 |
rs144069577 | snp | C/T | 0.107341 | 0.205301 | intron-variant | TLE2 | GRCh38.p7 | 19:3001876 | GATCTTGGCTCACTG[C/T]GACCTCCACCTCCCG | 7089 |
rs144080315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3015290 | CGTCTGGCAATGAGA[A/G]GAGGTCCCAGCCTCT | 7089 |
rs144170937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3001316 | GTTGGGATCTCACTA[C/T]GCTGCCCAGACTGGT | 7089 |
rs144177563 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3012780 | CCCCTGCCTCCCCTG[A/C]CTCCCAAGAAACTTC | 7089 |
rs144303942 | snp | C/T | 0.106278 | 0.204558 | intron-variant | TLE2 | GRCh38.p7 | 19:2998651 | ACTCCTGACCTCAGG[C/T]GATCCACCGCCTAGG | 7089 |
rs144337124 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TLE2 | GRCh38.p7 | 19:3016935 | AGGCGCCCACCACCA[A/C]ACCCAGCTAATTTTG | 7089 |
rs144436686 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3008778 | TTTCTAGAAGGGAAG[C/G]AGGGAGACCCCAACC | 7089 |
rs144443230 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3044450 | TTAGAGAAGGATTCC[C/T]GCTCTGTCGCCCAGG | 7089 |
rs144483017 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TLE2 | GRCh38.p7 | 19:3002288 | TATCTAAGATTCAGA[C/T]TGAATAGGCACCCTG | 7089 |
rs144546853 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | TLE2 | GRCh38.p7 | 19:3004894 | CAGGATCTGGGGTCA[C/G/T]GGTGCCTGAAGATTC | 7089 |
rs144558420 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3026977 | TCAGAAATTTGAGGT[A/C]TATCTCAGAACCCTG | 7089 |
rs144746815 | in-del | -/TGTG | | | intron-variant | TLE2 | GRCh38.p7 | 19:2998266 | TGTGTGTGTGTGTGT[-/TGTG]GTGTGTGTGTAATTT | 7089 |
rs144773444 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3010325 | GCTGAGATGGTGCCA[C/T]TGCACTCCAGCCTGT | 7089 |
rs144917343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3013563 | TGGACAATGCCAGCC[C/T]GGCTGGCTGATTTCT | 7089 |
rs144928446 | snp | C/T | 2.1933e-05 | 0.00331149 | missense | TLE2 | GRCh38.p7 | 19:3027866 | AGCCCGTACGACATC[C/T]CATAATACTGCAAAG | 7089 |
rs145105926 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | TLE2 | GRCh38.p7 | 19:3026281 | GAGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 7089 |
rs145182487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029799 | GTGCGCTATCTTTAG[C/G]GTTTAATTTTTTGCA | 7089 |
rs145201221 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | TLE2 | GRCh38.p7 | 19:2999759 | GAAAAACAGCTGGGC[A/G]CAGTGGCTCACGCCT | 7089 |
rs145250254 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3047080 | TCCCCCTCCCTCCAC[C/T]TCCCTCCTCTCTCTC | 7089 |
rs145264513 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:2998110 | AGTTTTGTTCTTGTC[A/G]CCCAGGCTGAAGTGC | 7089 |
rs145320559 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:2999102 | GACTGGCCAACGTGG[G/T]GAATCCCCGTCTCTA | 7089 |
rs145324089 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE2 | GRCh38.p7 | 19:3037525 | CCAGCTGTGAAGTGT[C/T]GGGGAGGTAGATACC | 7089 |
rs145388533 | snp | A/G | 3.60887e-05 | 0.00424771 | missense | TLE2 | GRCh38.p7 | 19:3002415 | AGCTGGTATTTCTCC[A/G]GCTTGCGGACGTGCA | 7089 |
rs145514117 | snp | A/G | 3.61978e-05 | 0.00425413 | synonymous-codon, intron-variant | TLE2 | GRCh38.p7 | 19:3009545 | CCAAGGACTCACCAC[A/G]GGGGAGCGTCCGTAC | 7089 |
rs145599349 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE2 | GRCh38.p7 | 19:3046217 | CCATGGGAAGAGAGC[A/G]GGATCATTTCTAGCT | 7089 |
rs145746063 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TLE2 | GRCh38.p7 | 19:2998556 | GTGTTGAGATTACAC[A/G]CATGAGCCACCGCAC | 7089 |
rs145901342 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3017736 | GGATCAAAGGCGTGA[A/G]CCACCATGATCGACC | 7089 |
rs145942000 | snp | C/G | 0.150333 | 0.229274 | intron-variant | TLE2 | GRCh38.p7 | 19:3041167 | GAGTAGCTGGGATTA[C/G]AGGTGCGTGCCACCA | 7089 |
rs145998658 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3020954 | ATTAGCCAGACGTGG[C/T]GGCGGGTGCCTATAA | 7089 |
rs146028211 | in-del | -/A | | | intron-variant | TLE2 | GRCh38.p7 | 19:3013988 | TCATCTGTAAAATGT[-/A]TTTTTTTTTTTTTTG | 7089 |
rs146082744 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3018822 | GGGGTTTTCCCATGT[A/T]GGCCAGGCTGCTCTC | 7089 |
rs146181850 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3031964 | ACGGAGTCTTGCTCT[A/G]CTGCCCAGGCTGGAG | 7089 |
rs146246666 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TLE2 | GRCh38.p7 | 19:3039340 | ACCTCTGTCTATGTG[A/T]TCTGACTTCCATCGC | 7089 |
rs146420626 | snp | A/C | 0.0607341 | 0.163335 | intron-variant | TLE2 | GRCh38.p7 | 19:3001957 | CGCCCACCACCACGC[A/C]TGGCTAATTTTTGTA | 7089 |
rs146424324 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | TLE2 | GRCh38.p7 | 19:3037243 | TGAGCCGAGTTCGCG[C/G]CACTGCACTCTAGCC | 7089 |
rs146560845 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TLE2 | GRCh38.p7 | 19:3013538 | TAAAAAAAAAAGCAC[A/C]GGGAAAGGGTGGACA | 7089 |
rs146606355 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TLE2 | GRCh38.p7 | 19:3033826 | CCTGGGCAACATAGC[A/G]AGACCCAACCCCCAC | 7089 |
rs146615644 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3017637 | TTGTATTTTTCTGTA[A/G]AGACGGGGTTTTGCC | 7089 |
rs146661635 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | TLE2 | GRCh38.p7 | 19:3032449 | CGCTATGTTGGCCAG[G/T]CTGGTCGCAAACTCC | 7089 |
rs146678500 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TLE2 | GRCh38.p7 | 19:3028254 | CAGGGACCTACCCCA[A/G]AGTCCACCGTGACTC | 7089 |
rs146797056 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE2 | GRCh38.p7 | 19:3037995 | AGCAAGGTGGCACAC[A/G]CCTGTAATCCCAGCT | 7089 |
rs146868641 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TLE2 | GRCh38.p7 | 19:3033155 | GCAGCTGGGATTACA[A/G]ACATACACCAAGCCT | 7089 |
rs147053625 | in-del | -/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3040351 | TTTAACGTTTGTTTG[-/T]TTTTTTTTTAAGACA | 7089 |
rs147069970 | in-del | -/TTA | 0.0733688 | 0.176922 | intron-variant | TLE2 | GRCh38.p7 | 19:3031857 | CTTCTGCCCACCCCG[-/TTA]TTTTCACACTCTCCA | 7089 |
rs147070656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3004202 | GTGTTTCTGTGTAAA[A/G]ACGCATTGGGGGACA | 7089 |
rs147077091 | in-del | -/C | 0.0210156 | 0.10033 | intron-variant | TLE2 | GRCh38.p7 | 19:3034633 | TGTCTCCTGCAAAAG[-/C]CTTCTCCCCCAGCCT | 7089 |
rs147140145 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3014468 | GCTGTCCCACAGAGC[A/G]GGGAACCAGGATCCC | 7089 |
rs147244927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030559 | TGTCCTTAGGTGATC[A/G]AGTACCTAATGGTAC | 7089 |
rs147333656 | snp | C/T | 0.000857633 | 0.0206901 | intron-variant | TLE2 | GRCh38.p7 | 19:3015917 | CAACGGCTGACTCAG[C/T]GCTAAGGTTTTGTTC | 7089 |
rs147356510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3018225 | CAGCCTCGAGTTCCC[A/G]GGCTCAAGTGATTGT | 7089 |
rs147400635 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TLE2 | GRCh38.p7 | 19:3027026 | TGAGGTCTATCTCAG[A/G]ACCTTGAGGTCTATC | 7089 |
rs147412730 | in-del | -/T | 0.478603 | 0.101197 | intron-variant | TLE2 | GRCh38.p7 | 19:2998278 | TGTGTGTGTGTGTAA[-/T]TTTTTTTTTTTTTTT | 7089 |
rs147423756 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031108 | TCTCTGAGTTTGTGG[A/G]ATGTGAGTGACAGGC | 7089 |
rs147459536 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:2999032 | TTGGCACGGTGGCTC[A/G]GCGCTTCCGGAGGCC | 7089 |
rs147508094 | in-del | -/AG | 0.0984431 | 0.198823 | intron-variant | TLE2 | GRCh38.p7 | 19:3017979 | CCCACCACCCCACTC[-/AG]AGTCTCTCTACCCTT | 7089 |
rs147529541 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049227 | TGCTGGGGTTACAGG[C/T]GTGTGCCAGCGTGTC | 7089 |
rs147611823 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | TLE2 | GRCh38.p7 | 19:2999261 | CACTCCAGGCTGGGC[A/G]ACAGAGAAGGACTCC | 7089 |
rs147616245 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997326 | AGAGTGCGACTGTCT[C/G]AAAAAAATTTCTACC | 7089 |
rs147685274 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE2 | GRCh38.p7 | 19:3007598 | AAAGGTGATATGGGA[C/T]AGTCAGTGGGTGGCA | 7089 |
rs147720997 | snp | C/T | 0.00548798 | 0.0520948 | intron-variant | TLE2 | GRCh38.p7 | 19:3009734 | GGGGACAGGTTTTGA[C/T]GCCCTGGACCCAGAT | 7089 |
rs147892494 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | TLE2 | GRCh38.p7 | 19:3038050 | TCCTTGGAACCCAGA[A/C]GGCGGAGGTTGCAGT | 7089 |
rs147948681 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3009151 | CTCTATCCAGGAAAT[C/T]CTAGAACTCCACGGT | 7089 |
rs147996138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3014344 | GGAAGGGGGTGTCAC[G/T]GCCCACAAATCACTC | 7089 |
rs148097259 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TLE2 | GRCh38.p7 | 19:3038129 | TCTGTCTCAAAAAAA[A/T]AATAATAACAATAAC | 7089 |
rs148136151 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TLE2 | GRCh38.p7 | 19:2999868 | TGAAACCCCCTCTCT[A/G]CTGAAAATACAAAAA | 7089 |
rs148153020 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3033616 | TCTTCCTTCTTCTGC[C/T]TAAGCCCCTGGCTCT | 7089 |
rs148262948 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | TLE2 | GRCh38.p7 | 19:3041846 | CTTTGGGGGCAGCCA[C/G]GCCCAGAGAGGCCTA | 7089 |
rs148311618 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | TLE2 | GRCh38.p7 | 19:3008151 | CATTTCAAGTACTGA[A/G]AGCCACGCCCAGCTG | 7089 |
rs148330387 | in-del | -/C | 0.0524604 | 0.153226 | intron-variant | TLE2 | GRCh38.p7 | 19:3003079 | TCTCCCTCTTCAGCA[-/C]CCCCCCTAGAGAAAG | 7089 |
rs148362640 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3003178 | CACAGAACCCTAGGG[C/G]TGCACATCCATTATC | 7089 |
rs148366349 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3018371 | GGACTTGGCTCACTG[C/G]AACCTCTGCCTCCCA | 7089 |
rs148411576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3009042 | CCTCTCTGTTTATCA[C/T]CCCTCCCCAAGGCAG | 7089 |
rs148533359 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TLE2 | GRCh38.p7 | 19:3016923 | AGCTGGGATTACAGG[C/T]GCCCACCACCACACC | 7089 |
rs148602558 | in-del | -/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3021115 | AAAAAAAAAAAAAAA[-/G]GGGGGGGGGTGCTGA | 7089 |
rs148621044 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE2 | GRCh38.p7 | 19:3039752 | CCCAGCATGACGGAC[A/G]CGATGCCAGGTCCCC | 7089 |
rs148697240 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE2 | GRCh38.p7 | 19:3001352 | ACTCCTGGCCTCAAG[C/T]GATCCTCCCACCGTG | 7089 |
rs148749484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:2998727 | AGAGCGACTTGTTTT[C/G]TACAGACAGGTGCTT | 7089 |
rs148855163 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | TLE2 | GRCh38.p7 | 19:2999671 | GGCAGAGCTTGCAGT[A/G]AGCAGAGATAGTGCC | 7089 |
rs148868785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3013892 | TCTCTATCCTCCTCC[C/T]GACTCCCACCCCAAT | 7089 |
rs148936473 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE2 | GRCh38.p7 | 19:3009979 | AACCTCTGCCTCCTG[A/G]GTTCAAGCAATTCTG | 7089 |
rs149058970 | snp | C/T | 0.00438332 | 0.0466095 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997379 | GAGTAGAGCCCCGTA[C/T]ACCATGTGGGTATGA | 7089 |
rs149061249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3028183 | GACCCTCCTAGAGAG[C/T]CTGAAATCCCAACCT | 7089 |
rs149183677 | snp | A/G/T | 0.00398755 | 0.0445055 | intron-variant | TLE2 | GRCh38.p7 | 19:3037574 | CCTGTGCCTACTTTC[A/G/T]CATGGGTCCTGAAGT | 7089 |
rs149220753 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TLE2 | GRCh38.p7 | 19:3002946 | TCAAGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 7089 |
rs149234305 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | TLE2 | GRCh38.p7 | 19:3044285 | CCCATGGAGGATCTC[C/G]ATAATCGCACATCTG | 7089 |
rs149325434 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3004798 | AGAGCTGTCCCGGAG[G/T]ATGGTGTGCATGAGA | 7089 |
rs149447742 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | TLE2 | GRCh38.p7 | 19:3011282 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCCAGT | 7089 |
rs149548374 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3035185 | CCAACTTTGGGAGCA[A/G]CGGGTGGAATTTGGG | 7089 |
rs149586321 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE2 | GRCh38.p7 | 19:2998645 | TCTCAAACTCCTGAC[C/T]TCAGGCGATCCACCG | 7089 |
rs149589773 | snp | A/G | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030501 | GGCACAGCTGGGAAC[A/G]AAACAGAGAAAAATC | 7089 |
rs149668076 | in-del | -/G | 0.0205511 | 0.0992634 | intron-variant | TLE2 | GRCh38.p7 | 19:3020430 | CAGACGTCTCCTGGT[-/G]GTAAAACTACCCCCA | 7089 |
rs149703049 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TLE2 | GRCh38.p7 | 19:3032183 | GTGATCCACCTGCCT[C/T]GGCCTCTCAAAGTGC | 7089 |
rs149708437 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3031965 | CGGAGTCTTGCTCTG[C/T]TGCCCAGGCTGGAGT | 7089 |
rs149739665 | snp | G/T | 0.00676609 | 0.0577691 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997148 | AGCCTAGTCAACATG[G/T]AGAAACATTGTCTCT | 7089 |
rs149760218 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TLE2 | GRCh38.p7 | 19:3045615 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 7089 |
rs149952293 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TLE2 | GRCh38.p7 | 19:3023690 | TTGAGTCCGGGGGTT[C/T]GAGACCAGCCCGGGC | 7089 |
rs150025940 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049418 | TCCAGGCAGAGGGAA[C/T]AGCATGTGAAAAGGC | 7089 |
rs150072484 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TLE2 | GRCh38.p7 | 19:3037459 | TTCCTGTGACAGAGT[A/G]AGCCTTGGGCTCTGA | 7089 |
rs150091357 | snp | A/G | 0.0116862 | 0.0755417 | synonymous-codon | TLE2 | GRCh38.p7 | 19:3025059 | CTGAGCGCAGATACC[A/G]CTCAGACGCTTCACA | 7089 |
rs150174941 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TLE2 | GRCh38.p7 | 19:3038452 | TCCTGGGCTCAAGCA[A/G]TCCTCTTCCCTCAGC | 7089 |
rs150197018 | in-del | -/CCCC | | | intron-variant | TLE2 | GRCh38.p7 | 19:3035661 | GGTTGGCTGGGGGCG[-/CCCC]CCAGCCAATCCGCTC | 7089 |
rs150404531 | in-del | -/GTGTGTAA | | | intron-variant | TLE2 | GRCh38.p7 | 19:2998271 | TGTGTGTGTGTGTGT[-/GTGTGTAA]TTTTTTTTTTTTTTT | 7089 |
rs150460487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030309 | TCAAGTCTCTCCCAC[A/G]GCAAAGGCTCCAGCC | 7089 |
rs150528416 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TLE2 | GRCh38.p7 | 19:3043938 | GCAGTGAGCCAAGAT[C/T]GCACCACTGCACTCC | 7089 |
rs150562401 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TLE2 | GRCh38.p7 | 19:3032047 | GCGATTCTCCTGCCT[C/T]GGCCTCTGGAGTAGC | 7089 |
rs150617881 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | TLE2 | GRCh38.p7 | 19:3026812 | TTATCTCTGACCCTT[A/G]AGGTCTATCTCTGAA | 7089 |
rs150619864 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3004509 | CCGAGCATGGTGGTG[C/T]GTTCCTGTAGTCCCA | 7089 |
rs150752053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3010747 | GGTCTGAAACCCAAG[C/T]CTGTCTGGCCCCAAA | 7089 |
rs150774760 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TLE2 | GRCh38.p7 | 19:3001499 | GAATGATTTTTTTTT[A/T]AAAAGAGATAGGGTC | 7089 |
rs150822935 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE2 | GRCh38.p7 | 19:3023370 | TCTTGCCTTTCTCTA[A/G]ACCACCTCGTCCCCA | 7089 |
rs150925287 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TLE2 | GRCh38.p7 | 19:3024456 | CTCTCACTCCCCGTC[C/T]CCTCCCCAACCCCTG | 7089 |
rs150980221 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3020784 | CTGTGGGACTCTGCT[A/G]CGAGAAAATGTTATA | 7089 |
rs151107177 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3040127 | TGCAGCAACCCCATC[A/G]CCCACACCACGTGTA | 7089 |
rs151139800 | snp | C/T | 0.00891513 | 0.0661671 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997614 | AGGAACAATGATCAC[C/T]GGTTCCCCAGCCCGA | 7089 |
rs151212215 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3017296 | GCACCCGCCGCCACG[C/T]TTGGCTAATTTTTGA | 7089 |
rs180690753 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3020423 | ACAACCACAGACGTC[G/T]CCTGGTGGTAAAACT | 7089 |
rs180695648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3039692 | TGTATTTATTGGGAG[A/G]GTAAGTGGACAAGCC | 7089 |
rs180697264 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3001902 | TCCCGGGTTCAGGCA[A/G]TTCTCCTGCCTCAAC | 7089 |
rs180720347 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3023466 | AGAAATCTCAGACTC[A/G]GTGGAATCTGAACAA | 7089 |
rs180918788 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3043686 | ATGGTGGCGGGCGCC[C/T]GTAGTCCCAGCTACT | 7089 |
rs180930091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3006938 | CAGGCATGCGCCACC[A/C]TGCCTGGCTAAGTTT | 7089 |
rs180931422 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3025202 | GGTGACGCCCGCAGG[C/T]GCACAGAGGGAACTC | 7089 |
rs181206289 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3034467 | CACCACACCCCCAAC[A/C]CCCTCCAGCCACCCT | 7089 |
rs181229585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3017334 | GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG | 7089 |
rs181245952 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3024447 | CCCATAAAACTCTCA[C/T]TCCCCGTCCCCTCCC | 7089 |
rs181251891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:2998945 | ACATTTTAGGCTTTG[C/T]CTAAAGTCTAAATAA | 7089 |
rs181261006 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3043260 | AGCTGAGACCACAAT[C/G]GTACACTACCATGCC | 7089 |
rs181337463 | snp | C/G | 0.00385284 | 0.0437216 | intron-variant | TLE2 | GRCh38.p7 | 19:3005691 | AGCGGCCGGGGGCTT[C/G]CCCAAGGTCCCAGCG | 7089 |
rs181368346 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3025497 | CCCCGGCTTGGCCCA[C/G]GTCTGTCCCAGGCAA | 7089 |
rs181373418 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | TLE2 | GRCh38.p7 | 19:3044388 | GCAGGATTCTACAGG[G/T]CTGGCCCACATCCAC | 7089 |
rs181480347 | snp | G/T | 0.114036 | 0.209795 | intron-variant | TLE2 | GRCh38.p7 | 19:2998290 | GTAATTTTTTTTTTT[G/T]TTTGTGAGACAGGGT | 7089 |
rs181481031 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TLE2 | GRCh38.p7 | 19:3007119 | TTGAGATGGAGTCTC[A/G]CTCTGTCACCCAGGC | 7089 |
rs181498602 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3033738 | CTCTTCCCTCTCTAA[G/T]CACAGGTGTGGTGGC | 7089 |
rs181626538 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TLE2 | GRCh38.p7 | 19:3016793 | TGAAATTTTTTTTTC[C/T]TTTGAGATGGAGTCT | 7089 |
rs181676713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3039168 | GCAGTGAGCTGAGAC[C/T]GTGCCATTGCACTCC | 7089 |
rs181683927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3001574 | CCCTACAGCCTCAAA[G/T]TCCTGGGCTCAAGCA | 7089 |
rs181685466 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE2 | GRCh38.p7 | 19:3019994 | CAGGTAGAATAGTTA[C/T]AAATCAGGCCGGGCA | 7089 |
rs181800902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3012349 | GCCTCCCAAGTAGCT[A/G]GCACTACAGGCACAC | 7089 |
rs181826798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3040360 | TGTTTGTTTTTTTTT[C/T]AAGACAGTCTCGCTC | 7089 |
rs181830799 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049237 | ACAGGTGTGTGCCAG[C/T]GTGTCTGGCTGGACT | 7089 |
rs181844489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3001981 | TTTTGTACTTTTAAT[A/G]GAGTCAGGGTTTCAC | 7089 |
rs182092394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3013288 | TCTCAGCTTGGGGCC[A/G]GTGTGTCTCTAAGCG | 7089 |
rs182336997 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3046743 | GGGGGGCTGGGAGAA[C/T]GGTGGGGTCGGAGAA | 7089 |
rs182341902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3008186 | CGACTGGGTTGGCCA[G/T]CAGTGGGTCTAGAAC | 7089 |
rs182344858 | snp | A/C | 0.021333 | 0.101051 | intron-variant | TLE2 | GRCh38.p7 | 19:3026948 | AGGTCTATCTCAGAA[A/C]CCTGAGGTCAATTTC | 7089 |
rs182369708 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE2 | GRCh38.p7 | 19:3011612 | CCCACCACTTTGGGA[A/G]GCCGAGGCCGGTGGA | 7089 |
rs182445483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3037404 | TTAGATTACCCTAAC[C/T]CTAAGTGGACAGAAG | 7089 |
rs182457841 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TLE2 | GRCh38.p7 | 19:3000502 | GCTTTAGTACCTGGG[C/T]GGTAGGGAGGCTTGC | 7089 |
rs182459485 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3018597 | CGTGCCTGGCTATCT[A/C]TTTTTATTTATTTAT | 7089 |
rs182636935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3017552 | GCCTTCTGGGCTCAA[A/G]TGATCCTCCCACCTC | 7089 |
rs182720090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:2999861 | AACATGGTGAAACCC[C/T]CTCTCTACTGAAAAT | 7089 |
rs182843267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030206 | CATCACCAGTGGACT[A/G]GGCTGTCTCCCCTCT | 7089 |
rs182918281 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3014666 | TGCCCCTGCCTCCAC[A/T]CCCCCTATCCGCTCC | 7089 |
rs182919754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3025776 | TCCTATTCCCACCAG[A/G]AGGGTGGAACTGGGA | 7089 |
rs182928118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:2999420 | ATTTCAATCACTGCT[A/G]ATGGGGATATAAAAT | 7089 |
rs182933373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3040683 | GACAAGGTCTCACTC[C/T]GTCGCCCAGGCTGGA | 7089 |
rs182936741 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997244 | AGGGAGAAGAATTGC[C/T]TAAGCCCAGGAGGCA | 7089 |
rs182944914 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE2 | GRCh38.p7 | 19:3021534 | TGATTAATTTTATTA[A/G]ATTTAAGTGAATACA | 7089 |
rs183179728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3041652 | CAATGGTCTTGACCT[A/G]TTTTCCAAACCTTCC | 7089 |
rs183184540 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TLE2 | GRCh38.p7 | 19:3046002 | AAGCACTGCTGGAGG[A/C]GTGATAGATGTTCAG | 7089 |
rs183220795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3007429 | TTCTCTGTTATTATT[C/T]TGTAGAGATGAGGTC | 7089 |
rs183227147 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TLE2 | GRCh38.p7 | 19:3003168 | ATCAGAATTACACAG[A/T]ACCCTAGGGCTGCAC | 7089 |
rs183439247 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | TLE2 | GRCh38.p7 | 19:3021835 | TGATTTGCCCCCCTC[A/T]GCCTCCCAAAGTGCT | 7089 |
rs183446829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3018049 | ATTCAGATCAATGCC[C/T]AGAGAGGGATAGTGA | 7089 |
rs183532492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3047179 | CTCCCCCTACCCTCC[C/T]CCGTCCTCCGCCTCA | 7089 |
rs183625835 | snp | C/G/T | 7.54809e-05 | 0.00614294 | intron-variant | TLE2 | GRCh38.p7 | 19:3027899 | AAAACCAAGTAAGAA[C/G/T]GTCTAGGGTGGAGAT | 7089 |
rs183630602 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048804 | ACAGGCTTGAACCAC[C/T]GCGCCCGGCCTGCTT | 7089 |
rs183632128 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TLE2 | GRCh38.p7 | 19:3010399 | AAACAAAACCCAGGC[C/G]CAATGTCCATTAACA | 7089 |
rs183720454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3031814 | CTACCTCCTCAGAAC[A/G]GCCCCTCCTAGCCAC | 7089 |
rs183737547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3002655 | GAGATCCTCCTGCCT[C/G]AGCACCAGAAGCTGA | 7089 |
rs183795474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031087 | AAGGGAGACAGATCC[C/T]TGCCCTCTCTGAGTT | 7089 |
rs183808450 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:2999760 | AAAAACAGCTGGGCG[C/T]AGTGGCTCACGCCTG | 7089 |
rs183988682 | snp | C/G | 3.38799e-05 | 0.00411568 | missense | TLE2 | GRCh38.p7 | 19:3013803 | TAGCCGGGCTGGGGG[C/G]CTCTGAGGGTTGGTC | 7089 |
rs184039665 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3039279 | TCCCTTGCTCAAGAA[C/T]CTTCCATAGCTCCCT | 7089 |
rs184048611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3019995 | AGGTAGAATAGTTAC[A/T]AATCAGGCCGGGCAT | 7089 |
rs184079127 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3036899 | TTAGGGAGGATCAGA[G/T]CTGGGGGTGGGAGTG | 7089 |
rs184123537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3032343 | TCTGGGCTCAGGTGA[C/T]TCTCCTGCCTCAGCC | 7089 |
rs184141676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3016029 | GAGACCCCCGCCTCC[C/T]GGGTTCAAGCGATCC | 7089 |
rs184146563 | snp | A/G | | | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997608 | CCCAAGAGGAACAAT[A/G]ATCACCGGTTCCCCA | 7089 |
rs184211181 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | TLE2 | GRCh38.p7 | 19:3027004 | CCTGAGGTCAATCTC[A/T]GAGCCCTGAGGTCTA | 7089 |
rs184380347 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE2 | GRCh38.p7 | 19:3019163 | TCGGCCTCCCAAATT[A/G]TTGGGATTATAGGCA | 7089 |
rs184512364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3038270 | TGGAGTGCAGTGCCA[C/T]CGTCATAGCTCACTG | 7089 |
rs184514427 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TLE2 | GRCh38.p7 | 19:3001130 | ATACAAAAATCAGCT[A/G]GGCATTGTGGCAGGC | 7089 |
rs184557805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3042987 | AGTTTTTAATTAATT[A/T]ATTTTTTATTTTTTA | 7089 |
rs184646450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3027156 | CTCAGAACCCTGAGG[C/T]CTATTTCAGAACCCT | 7089 |
rs184767659 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3047965 | CGGGCTGCGGTGTCT[C/G]TCGCCTGTAATCCTC | 7089 |
rs184786291 | snp | A/G | 0.000174871 | 0.00934906 | intron-variant | TLE2 | GRCh38.p7 | 19:3009522 | GCTGACACCTCCTGC[A/G]CCCCCACCCAAGGAC | 7089 |
rs184799660 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TLE2 | GRCh38.p7 | 19:3042491 | GGCGGGAGCGGGGAC[C/G]GGGATGGTAGGGAGG | 7089 |
rs184820692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3003746 | GTCTTGCTCTGTCGC[C/T]CAGGCTGGAGTGCAG | 7089 |
rs184827697 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3022626 | GGGGCTGGTGACTGC[C/T]GTGTAGGATAGCGGA | 7089 |
rs184900762 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3043402 | TGAGATGGTCTCGAA[C/T]GCCTAACCTCGTGAT | 7089 |
rs184934433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3006816 | GAGAGGGAGTCTCGC[C/T]GTGTCGCCCAGGCTG | 7089 |
rs185031138 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TLE2 | GRCh38.p7 | 19:3024546 | TGGATCACCCAGTGT[C/T]TGTCCCTCAGTGACT | 7089 |
rs185048550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3038997 | GCAGTGAGCTGAGAT[C/T]GCACCATTGCACTCC | 7089 |
rs185073091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3019829 | CCTGCTCATGCTAGC[A/G]GTGCCCTTGGGGACC | 7089 |
rs185188250 | snp | C/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3024303 | GAGCCACCGCACCTG[C/G]CCGAATTACAGTCCA | 7089 |
rs185277345 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3030626 | TTACAAAAGGGCACA[A/G]GAGCCCTTATCAATG | 7089 |
rs185299068 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3013303 | GGTGTGTCTCTAAGC[A/G]CCTCTGGAAGGGCTC | 7089 |
rs185310885 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3004263 | ATCCCTAGAAATGTT[C/T]TTAGCCCACCTAAGC | 7089 |
rs185443956 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TLE2 | GRCh38.p7 | 19:3033376 | GTTTCACCATGTTAG[C/T]CAGGATGGTCTCAAT | 7089 |
rs185446388 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:2998150 | ATCTTGGCTCACTGC[A/C]ACCTCCACCTCCCGG | 7089 |
rs185559714 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | TLE2 | GRCh38.p7 | 19:3012891 | GAGAGAGTGGATGGG[A/G]CGACTGTGGGGTCAG | 7089 |
rs185581990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3016602 | CTCAAAAAAAAAAAA[A/G]AAAAATTAAACCATT | 7089 |
rs185740856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3009092 | CCTGTCACACTACAG[A/G]TGAGAGGGCTGAGGT | 7089 |
rs185812674 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | TLE2 | GRCh38.p7 | 19:3034542 | CTTTCCCTGCTTGTT[A/C]TCTCTTCCTGGAATT | 7089 |
rs185832694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3017419 | CTGGGATTACAGGCA[C/T]GCACCTGGCCTGGTT | 7089 |
rs185943323 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3020617 | AATTCTGCCTCCTAC[A/G]ATCGCCTTCCTAAAC | 7089 |
rs186061898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3040131 | GCAACCCCATCACCC[A/T]CACCACGTGTAACCC | 7089 |
rs186086289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3034162 | CTAAACCAGAGCATC[A/C]CCCTAGCCCTCTATT | 7089 |
rs186095859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3017031 | GATCCACCCACCTTG[C/G]CCTCCCAAAGTACTG | 7089 |
rs186096743 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3001942 | AGCTGGGATTACAGG[C/T]GCCCACCACCACGCC | 7089 |
rs186116006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:2998586 | CCCGGCCTAATTTTT[G/T]TATTTTTAGTAGAGA | 7089 |
rs186119385 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TLE2 | GRCh38.p7 | 19:3043853 | GCCAGGCATGGTGGC[A/G]GGGGCCTGTAATCCC | 7089 |
rs186127718 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3007013 | TGGTTTTGAACTCCT[A/T]ACCTCAAGTGATCTG | 7089 |
rs186210105 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029703 | CCAGAAAGGGAATCT[C/T]ACAGCAAACACTGCT | 7089 |
rs186231145 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE2 | GRCh38.p7 | 19:3001712 | ACTCCTGGTCTTGGG[C/T]GATCCTTCTGCCTTA | 7089 |
rs186374736 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3040478 | CCCGAGTAGCTGGGA[C/T]TACAGGTGCACACCA | 7089 |
rs186386394 | snp | C/T | 1.68843e-05 | 0.00290549 | intron-variant | TLE2 | GRCh38.p7 | 19:3002335 | TGAGGGCGTGCCACC[C/T]CGCCCCAGAAGACAC | 7089 |
rs186464854 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3046092 | CTGGTTGCCCCTAGG[A/G]GGGCAAAGAGGTCCC | 7089 |
rs186702590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:2999015 | TTTGAAAATATAAAG[A/G]GTTGGCACGGTGGCT | 7089 |
rs186729900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3025598 | TCAGCACGCCACACT[C/G]AAGGGAAGGATTTCA | 7089 |
rs186830740 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3031855 | AGCTTCTGCCCACCC[C/T]GTTATTTTCACACTC | 7089 |
rs186838755 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE2 | GRCh38.p7 | 19:3015137 | ATATTGGCCCACCCT[A/G]AGCCTGCCAGTCTCC | 7089 |
rs186847188 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997309 | TCTCCAGCCTGGGAG[A/G]CAGAGTGCGACTGTC | 7089 |
rs186952775 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3044902 | ATAAATTGTGCGGAG[C/T]AAAAAATGCTGTGAA | 7089 |
rs186968731 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE2 | GRCh38.p7 | 19:3007338 | CAAATGATCCTCCCA[C/T]CTCGGCCTCCCAAAA | 7089 |
rs187031294 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TLE2 | GRCh38.p7 | 19:2999626 | CAGCTACTCGGGAGG[A/C]TGAGGCAGGAGAATG | 7089 |
rs187089939 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3037643 | GCCCGTGGTAGGAGG[A/C]ACTAGGATTGGCTGA | 7089 |
rs187225230 | snp | C/T | 1.67666e-05 | 0.00289534 | intron-variant | TLE2 | GRCh38.p7 | 19:3017796 | CAGAACCAGCGTTGG[C/T]CTCCCAAGAATATAA | 7089 |
rs187285533 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3007677 | ACTTAATAAATGTTC[A/G]TTCAACCGAGGACCC | 7089 |
rs187323324 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3049398 | GGAAATAAAGAGAAC[A/C]CTGTTCCAGGCAGAG | 7089 |
rs187327222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3037072 | GGCGGATCACCTGAG[A/G]CCAGGAGTTCGAGAC | 7089 |
rs187345778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3018059 | ATGCCCAGAGAGGGA[C/T]AGTGACTTGCCTCAA | 7089 |
rs187362267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3011970 | ACATGATCAGACAGG[C/T]GCTGTGGCTCACGCC | 7089 |
rs187606085 | snp | A/G | 0.365508 | 0.221716 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029383 | CCTCCCCGCGCCCGC[A/G]CCCCCCCCGGCCCCC | 7089 |
rs187703977 | snp | A/C | 0.021333 | 0.101051 | intron-variant | TLE2 | GRCh38.p7 | 19:3026949 | GGTCTATCTCAGAAC[A/C]CTGAGGTCAATTTCA | 7089 |
rs187713247 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3047069 | CCTCCCCTCCCTCCC[C/T]CTCCCTCCACTTCCC | 7089 |
rs187714494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3008352 | GTGACAACCACACGT[G/T]TCCCCCGACATCGCC | 7089 |
rs187806350 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3041864 | CCAGAGAGGCCTAGG[A/G]ACCTGCCCACGGTCA | 7089 |
rs187820131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3041380 | CACACCATGGCCCTC[C/T]GAATTATGGGCTGAG | 7089 |
rs187839569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3003599 | CCTGAGATTGCACCA[C/G]TGCACTCCAGCCTGG | 7089 |
rs187964193 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TLE2 | GRCh38.p7 | 19:3042651 | GCGAGGCGAGGGAGA[A/T]TGTTGGATAATCTGT | 7089 |
rs187972993 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TLE2 | GRCh38.p7 | 19:3003927 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 7089 |
rs188075819 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TLE2 | GRCh38.p7 | 19:3019103 | GGGTCTCGCTCTGTT[G/T]CCCAGGCTGGTCATG | 7089 |
rs188081597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3032582 | ACTCGGAGGTTGTTC[A/G]CGTCCTTGTTTGTCT | 7089 |
rs188085634 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3006865 | TCAGCTCACTGCAAC[C/T]TCTGCCTCCTGGGTT | 7089 |
rs188092144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3021574 | ATAAAATAAATTTAA[C/T]AGGCTTATTTTTATT | 7089 |
rs188101989 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | TLE2 | GRCh38.p7 | 19:3016054 | CGATCCTCCTGCCTC[A/G]GCCTCCCCAGTAGCT | 7089 |
rs188317829 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TLE2 | GRCh38.p7 | 19:3027007 | GAGGTCAATCTCAGA[A/G]CCCTGAGGTCTATCT | 7089 |
rs188330462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3028024 | CGGGGTCCCAGAGGA[A/G]GAAGCGGGGGCTCTG | 7089 |
rs188334503 | snp | A/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048811 | TGAACCACCGCGCCC[A/G/T]GCCTGCTTTTGTTTT | 7089 |
rs188348314 | snp | C/T | 0.00121161 | 0.0245832 | synonymous-codon | TLE2 | GRCh38.p7 | 19:3011110 | GGAAGCGTCCTGGGG[C/T]GGGGAGGAGTCACAG | 7089 |
rs188353112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3000545 | AGGGGTTAGGGTGGC[A/G]GGGGGACCTGGGGGA | 7089 |
rs188375693 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3026065 | ATGAAGCTCAGAAGT[G/T]TGGGACCCCTCTCAT | 7089 |
rs188581871 | snp | G/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3021118 | AAAAAAAAAAAAGGG[G/T]GGGGGGTGCTGAGCG | 7089 |
rs188586855 | snp | A/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3047695 | CCTAAGGGTCGGAGA[A/T]GAGGAGCCCCAAGTA | 7089 |
rs188587626 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3038386 | GCTAATTTAAAAAAA[A/T]TTTTTTTGTAGAGAC | 7089 |
rs188609899 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3010101 | GAGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7089 |
rs188613950 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TLE2 | GRCh38.p7 | 19:3027190 | GTCTGTCTCAGAACC[C/T]TGGATCACACTGAGA | 7089 |
rs188620874 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3009335 | GCTTAATCGCTGTTG[C/T]GTTTTTCCACAATCA | 7089 |
rs188857566 | snp | A/G | 0.000164976 | 0.00908078 | intron-variant | TLE2 | GRCh38.p7 | 19:3019245 | GTCCTCCCCAGCCCC[A/G]TCTCCCCAGCCAATG | 7089 |
rs188883416 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3014166 | CTCAAGTGATCCATT[C/T]GCCTCAGCCTCCCAA | 7089 |
rs188991092 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3039070 | AAAAATTAAAAAAAA[A/T]AAATTAGCTGGGTGT | 7089 |
rs189010204 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE2 | GRCh38.p7 | 19:3019857 | ACCTGACCTCTCCCC[A/G]CCACCCTCTCATCTT | 7089 |
rs189016507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3001538 | TTGCCCAGGCTGGAG[A/G]GCAGTGATGTCATCA | 7089 |
rs189117101 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997632 | TTCCCCAGCCCGAGA[C/G]AGAAGTGCGGATGTG | 7089 |
rs189165664 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997199 | CTGGGTGTGGTGGTG[G/T]TCCTGTAATCCCAGC | 7089 |
rs189237279 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | TLE2 | GRCh38.p7 | 19:3034225 | TCCCCACCCCAGCAG[A/C]CCCCACCCTGACCAG | 7089 |
rs189245535 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TLE2 | GRCh38.p7 | 19:3017079 | GCCTTCTGGGTATCT[C/G]CCACACAGAAAGGCT | 7089 |
rs189266350 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:2998615 | GACTGGGTTTCCCCA[C/T]GTTGGCCAGGCTAGT | 7089 |
rs189361109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3043519 | AACATCTACCTGGGA[C/G]CTGCATCATGGGTCG | 7089 |
rs189384095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3005096 | AAGTGTGTGTCCCGC[A/G]CTCTCGGCGGCGTCC | 7089 |
rs189612315 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:3020140 | ACTCAGGAGGCTGAG[A/G]CAGGAGAATCGCTTG | 7089 |
rs189641246 | snp | A/G | | | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048199 | TCATGCCACTGCATG[A/G]TCTGGGCGACAGAGC | 7089 |
rs189721779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3046348 | CAGCCAGCGCAGGCA[C/T]CTGGCCGGCCTGACT | 7089 |
rs189731299 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3007911 | CCAACATGGTGAAAC[A/C/G]CTGTCTCTACTAAAA | 7089 |
rs189732786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3026518 | TGAGATCAGAAGTTC[A/G]GGAATAGCCTCAGAA | 7089 |
rs189894695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3039292 | AACCTTCCATAGCTC[C/T]CTATTGCCCTCAACA | 7089 |
rs189896283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3001955 | GGCGCCCACCACCAC[A/G]CCTGGCTAATTTTTG | 7089 |
rs189896758 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TLE2 | GRCh38.p7 | 19:3001877 | ATCTTGGCTCACTGC[A/G]ACCTCCACCTCCCGG | 7089 |
rs189899504 | snp | A/G | 0.114387 | 0.210022 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029447 | GTTGGGGAAACTGAG[A/G]CCGGGTGGGGAGGCG | 7089 |
rs189986345 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3031067 | CAGGGATTGTAAGGG[C/T]GGATAAGGGAGACAG | 7089 |
rs190161394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3012239 | CCCTGGGTGACAGAG[C/T]GAGACTCCATCTCCA | 7089 |
rs190184988 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3043207 | GATCACGGCTCCCTG[C/T]GAGGCTCAAGCAATC | 7089 |
rs190211569 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TLE2 | GRCh38.p7 | 19:3001230 | GTGAGCTGAGATTGC[A/G]CCACTGCACTCCAGC | 7089 |
rs190271919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3012971 | TGTAAGGTTTTTCCC[A/G]CAGTGGGAGGTGGGC | 7089 |
rs190278159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3029871 | GGGCAATCATGGCTC[A/G]CTGCAGCCTCGAACT | 7089 |
rs190392633 | snp | A/G | 0.000152768 | 0.00873846 | missense | TLE2 | GRCh38.p7 | 19:3002422 | ATTTCTCCGGCTTGC[A/G]GACGTGCAGGATCTC | 7089 |
rs190394821 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE2 | GRCh38.p7 | 19:3021359 | GCAGTGAGCCAAGAT[C/T]GTGCCATGCACTCCC | 7089 |
rs190423254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3024328 | AGTCCATTTTAACCA[C/T]TTGTAAGTGCACAGC | 7089 |
rs190444058 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TLE2 | GRCh38.p7 | 19:3016715 | GCGAACGGAAGTGAG[G/T]ATGGGAAGAAGGGTC | 7089 |
rs190622233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3037167 | GCACGCTCCTGTAGT[C/G]CCAGCTACTCAGGAG | 7089 |
rs190686009 | snp | A/G | | | intron-variant | TLE2 | GRCh38.p7 | 19:2999098 | ACCAGACTGGCCAAC[A/G]TGGGGAATCCCCGTC | 7089 |
rs190691280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3033729 | CGGGCGGCCCTCTTC[C/T]CTCTCTAAGCACAGG | 7089 |
rs190700161 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | TLE2 | GRCh38.p7 | 19:2998177 | CCGGGTTCAAGACAC[A/T]CTCCTGCCTCAGCCT | 7089 |
rs190920791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3025301 | CCCAGGGTGGCCTGG[A/G]GCTGGGAAGACCAGG | 7089 |
rs190923034 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TLE2 | GRCh38.p7 | 19:3044136 | CGAGACCTTGCCACT[A/G]CCCTCCAGCCTGGGC | 7089 |
rs190926806 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE2 | GRCh38.p7 | 19:2999706 | CACTCCAGCCTGGGT[A/G]ACAGAGTGAGACTCC | 7089 |
rs190929703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3007032 | TCAAGTGATCTGCCC[A/G]CCTCGGCCTCCCGAA | 7089 |
rs190940099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3017500 | CTGTCACCCAGGTTG[C/G]AGTGCAGTGGCACGA | 7089 |
rs190940339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3013493 | TTAATATTTACTGAG[A/G]TTCAACAAAGTCAGT | 7089 |
rs191119288 | snp | C/T | 0.0115144 | 0.0749975 | upstream-variant-2KB | TLE2 | GRCh38.p7 | 19:3048584 | TCAAGGGCATGATCT[C/T]GGCTCACTTCAACCC | 7089 |
rs191127231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3010240 | ATGGTGGTGCATGCC[C/T]GTAATTCCAGCTACT | 7089 |
rs191131484 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3027760 | CCCCGGCTGCCCACT[A/C]TGGGTCCTTCTCAGG | 7089 |
rs191186259 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3021652 | CAATGGCATGCTCTT[A/G]GCTCACTGCAACCTC | 7089 |
rs191191595 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE2 | GRCh38.p7 | 19:3020840 | CCTGTAATCACAGCA[C/T]TTTGGGAGGCCAAGG | 7089 |
rs191431651 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TLE2 | GRCh38.p7 | 19:3041561 | GGCCTCCCCTCCTCT[C/T]CTGGGCCAAGCAGCC | 7089 |
rs191444781 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE2 | GRCh38.p7 | 19:3002951 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 7089 |
rs191559207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3022611 | TGTAAATGATCACAC[A/G]GGGCTGGTGACTGCC | 7089 |
rs191569895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3003639 | CAAGACTCTGTCTCA[A/G]AAACAAAAAACAAAA | 7089 |
rs191658886 | snp | C/T | | | intron-variant | TLE2 | GRCh38.p7 | 19:3031950 | TTTTGTTTTTTGAGA[C/T]GGAGTCTTGCTCTGC | 7089 |
rs191668168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3015815 | CCCTGGGCTCCTAGA[C/T]TGCATTGTGATCCAG | 7089 |
rs191682590 | snp | A/C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TLE2 | GRCh38.p7 | 19:2997589 | TTGCCTCCCAGTAAC[A/C/T]GTGCCCAAGAGGAAC | 7089 |
rs191728352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3045056 | GACCTTGTCCCTACA[A/C]AAAAAAAATTAGCTG | 7089 |
rs191759557 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | TLE2 | GRCh38.p7 | 19:3007359 | CCTCCCAAAATGCTG[C/G]GATTACAGGCATGAG | 7089 |
rs191977002 | snp | C/G | 0.0160643 | 0.0881709 | intron-variant | TLE2 | GRCh38.p7 | 19:3017890 | TGGGATAAAGAGAAA[C/G]AAGGAGAAAGAATGA | 7089 |
rs192000227 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TLE2 | GRCh38.p7 | 19:3042926 | GAGGGGAATCCTAGG[A/C]CCTCAGAGGGGAAAC | 7089 |
rs192008450 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3004041 | ATTCAGGGTCCTCCA[C/T]CTCATTTTAAGCACA | 7089 |
rs192014425 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | TLE2 | GRCh38.p7 | 19:3024052 | CCAGGCTGGAGTGCA[C/G]CGGCGCAATCTCTGC | 7089 |
rs192036721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE2 | GRCh38.p7 | 19:3025646 | CCCAGGTGCCCCAAA[C/G]AGGCTGAGCAGACGA | 7089 |
rs192191578 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3037681 | AGGAACTCCAGCCTC[G/T]CCCTGAGTAAGAACT | 7089 |
rs192194217 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE2 | GRCh38.p7 | 19:3001041 | ACTTTGGGAGACAGA[A/G]GTGGCTGGGTCACTT | 7089 |
rs192249343 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE2 | GRCh38.p7 | 19:3018347 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGACTTG | 7089 |
rs192255183 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | TLE2 | GRCh38.p7 | 19:3000434 | TAAATTTTAGAAAAA[C/G]CAACAGGCTACGGGC | 7089 |
rs192315448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE2 | GRCh38.p7 | 19:3036650 | ACATTTCCTTCCACC[C/T]AGGAACATGAGGAGC | 7089 |
rs192437190 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE2 | GRCh38.p7 | 19:3041970 | TAGGGCAGGGTCGCC[C/T]GCCCCCTCCTCCCGC | 7089 |
rs192442531 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE2 | GRCh38.p7 | 19:3016098 | CCACCACCACGCCCA[A/G]CTAATTTTTGTATTT | 7089 |
rs192502076 | snp | A/G | 0.000656383 | 0.0181042 | intron-variant | TLE2 | GRCh38.p7 | 19:3019490 | GAGGCAGGATGGGCC[A/G]GGGCGGGGGGCGGCA | 7089 |