SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs118014419 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81614617 | TTCATCCCTCCCAAC[C/T]GGTAAAATGGGATAA | 7088 |
rs118032064 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | TLE1 | GRCh38.p7 | 9:81645097 | GGGTGCAGTGCCTCA[C/T]GTCAGTAATCCCAGC | 7088 |
rs118046135 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | TLE1 | GRCh38.p7 | 9:81671344 | CATGGCGAAACCCTG[C/T]CTCTATTTAAGAAAA | 7088 |
rs118092318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81664486 | ATTCATCTTTAAATC[C/T]AATGTGTCTGAGTAG | 7088 |
rs118140921 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TLE1 | GRCh38.p7 | 9:81667222 | GTTTGAGACCAGCCT[A/G]GCCAACATGGCTAGA | 7088 |
rs118145750 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | TLE1 | GRCh38.p7 | 9:81668097 | TTGAACCCAGGAGAC[A/G]GAGGTCGCGATGAGC | 7088 |
rs118170968 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | TLE1 | GRCh38.p7 | 9:81663241 | TGCTGAGACACAACA[A/T]TGCTGGCAAACCTGG | 7088 |
rs137866248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664137 | ATACCTAAAGAAAGT[C/T]AGGAGCCAGGCATGG | 7088 |
rs137870053 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81601023 | TCAGTCTACACAGTC[A/G]TGTGAGCCAATCCCT | 7088 |
rs138018906 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | TLE1 | GRCh38.p7 | 9:81642580 | GTGCCTATAATCCCA[C/G]CTACTCCAGAGGCTG | 7088 |
rs138071852 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81614532 | CTACAGCGTGGCAAA[A/G]AGCACGGGCTAAAGA | 7088 |
rs138086663 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81604344 | GAGCAGGTGATGTGG[A/G]AACCCTAAACCATGG | 7088 |
rs138107003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675999 | CCACCACACCAGGCC[G/T]ACCCACACTAGTTTT | 7088 |
rs138111096 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81610650 | TGGGGCCAAACAGTT[A/C]TTTTCTTTGTTAGGG | 7088 |
rs138149877 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686843 | TTCTTTATACTATTA[C/T]ACCCACCTCCCTCAC | 7088 |
rs138174927 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81617893 | GCTGGGTTTAGTGGC[A/G]TGCATCTGTTAATCC | 7088 |
rs138184989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645785 | AAAAATAAATGCTTG[A/T]GGGGATAGATACCCC | 7088 |
rs138221961 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | TLE1 | GRCh38.p7 | 9:81643343 | CTGGGTTCAAGCGAT[G/T]CTCCTGCCTCAGCCT | 7088 |
rs138237725 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634106 | TCTCACCTCTGTGGT[A/G]CTCTGCATCGTGGTG | 7088 |
rs138279138 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81622221 | GTTTACTTCAGCCCC[C/G]AGGTCTCCTCCTCCA | 7088 |
rs138314949 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81683037 | AATTATACCATTCTT[C/G]ATTTGGATGCACTTT | 7088 |
rs138371546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81656534 | TAACCCTGAGCCCAT[C/T]ATCCAAGGATAAGCA | 7088 |
rs138432551 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81601243 | AAAGGGGGAAGCCCC[C/T]GGCCACTGAAACTTT | 7088 |
rs138448561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81600216 | TAAACTAAAAAATTC[C/T]AGCAAAGGAACTATC | 7088 |
rs138448733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665074 | AAGATCAGAACAAGA[C/T]AGTGGAGAGGAGAGG | 7088 |
rs138449225 | snp | C/G | 0.0015226 | 0.0275496 | intron-variant | TLE1 | GRCh38.p7 | 9:81653934 | TTGCAAACAGAGAAG[C/G]AACATAATTGCACTT | 7088 |
rs138469276 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | TLE1 | GRCh38.p7 | 9:81597169 | ACACAGAGGTCGCAG[G/T]GGTTGCTGTAAGGAT | 7088 |
rs138513787 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81630171 | AGTTCGTCTTATTTA[C/T]GGCCAAAGGTTCTCA | 7088 |
rs138531622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626379 | TGCCTTCTCCATCTA[C/T]ACCTGGTGTCAATCA | 7088 |
rs138552622 | in-del | -/T | 0.0232847 | 0.105357 | intron-variant | TLE1 | GRCh38.p7 | 9:81680742 | AAGAACAGGCCTGGC[-/T]TAATGAAGTTGAGGA | 7088 |
rs138611051 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81645534 | TCCCCTGAGGTCAGG[A/C]GCTCCAGATCAGCCT | 7088 |
rs138710557 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638014 | CAATCATGTTCTCCA[C/G]AATAAGAAAGGAAAA | 7088 |
rs138721625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586386 | AGAGTGGAGCCTATC[A/G]CTTGTAGGCTACAAC | 7088 |
rs138753856 | snp | A/C | 0.0111196 | 0.0737302 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584090 | GTCAAGGTTTGGAAA[A/C]AGGTGTTTGTAATTT | 7088 |
rs138795312 | snp | A/C | 0.00188375 | 0.0306321 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634275 | TCCGTGGCCATGAGA[A/C]AGATGCTGAGCTTGC | 7088 |
rs138798866 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81614840 | TCTATGACATGCCCC[A/G]ATATTAAGGATCAGT | 7088 |
rs138803793 | snp | G/T | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690996 | ACCGTCAGTATTGCC[G/T]CATTTATGCTTTTGT | 7088 |
rs138804277 | in-del | -/G | 0.0592355 | 0.161582 | intron-variant | TLE1 | GRCh38.p7 | 9:81623933 | CTCCTCCTGCTCCTT[-/G]TAATCTGGAGGACTA | 7088 |
rs138813120 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81679650 | GTCAAATAAGCCCAC[C/T]GACAGAAACAGCTGT | 7088 |
rs138818364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611410 | AAAATGAATGAAAAG[C/G]CTTCTGTGAACCACT | 7088 |
rs138832065 | snp | A/C | 0.0633504 | 0.166319 | intron-variant | TLE1 | GRCh38.p7 | 9:81675727 | TTTTTTTTGAGACGG[A/C]GTCTCGCTCTGTCGC | 7088 |
rs138897206 | in-del | -/CT | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81639395 | AACCAAAACCTGCCC[-/CT]GTCATTTGGAAAACT | 7088 |
rs138913430 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TLE1 | GRCh38.p7 | 9:81594521 | GCACTCCAGCCTAGG[C/T]GACAAGAGCAAGACT | 7088 |
rs138933671 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81626004 | CTTCATGAATCCTAA[A/G]ACCTCCAAGCAACTT | 7088 |
rs139039794 | snp | C/G | 1.71003e-05 | 0.00292401 | missense | TLE1 | GRCh38.p7 | 9:81610263 | TTGGAGGAATGGTAG[C/G]TACTCTCATGTGAGG | 7088 |
rs139042775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619669 | AGAATGCATCCATCC[C/T]GAAACAGACACTCAG | 7088 |
rs139049852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688065 | CGGCCCACTCCCCAC[C/T]CCAGGAAGAGAGGGC | 7088 |
rs139072711 | snp | C/G/T | 0.000166542 | 0.00912377 | synonymous-codon, missense, splice-acceptor-variant, intron-variant | TLE1 | GRCh38.p7 | 9:81634299 | AGCTTGCAACTGCTG[C/G/T]TGCTGTTGGTGGTGG | 7088 |
rs139111374 | snp | A/C/G | 8.86288e-05 | 0.00665639 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611928 | AGCAGGATATGGGCC[A/C/G]GGCACTGCCAGGGGT | 7088 |
rs139123743 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81621395 | GAGTTCTTTTAAGTG[C/T]GGGATTAGCATATGC | 7088 |
rs139183942 | snp | G/T | 0.000131785 | 0.00811635 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81584270 | CTTATCATCCACAGA[G/T]ATGTCACAGCTAAGC | 7088 |
rs139193408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81662001 | GAAATTATTCAAACC[C/T]GTTGGTAAGGCTTCC | 7088 |
rs139213713 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81618211 | AATTCTTGGAAAGGA[A/C]GAGGTCCTGAATTTA | 7088 |
rs139215768 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81659964 | TCCCCCATAACGCCA[A/G]TAAACGCACTCTTCT | 7088 |
rs139230876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81655669 | ACTAAATGCCACCTA[C/T]ATTACTGAATTAAGC | 7088 |
rs139237489 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TLE1 | GRCh38.p7 | 9:81607767 | ATTCCCAAGAAAACA[C/T]ACCAGGTAGTAACTA | 7088 |
rs139251920 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | TLE1 | GRCh38.p7 | 9:81656839 | CAACTCTGTCAAATA[C/T]GCCTCCACACAGATC | 7088 |
rs139267143 | snp | C/T | 0.031825 | 0.122064 | intron-variant | TLE1 | GRCh38.p7 | 9:81592274 | GAGGCAGGAGAACGG[C/T]GTAAACCCCGGAGGC | 7088 |
rs139285051 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81667962 | TGAGGCCAAGAGTTC[A/G]AGATCAGCCTGGCCA | 7088 |
rs139328166 | in-del | -/C | 0.0325976 | 0.123435 | intron-variant | TLE1 | GRCh38.p7 | 9:81624002 | CGGCTCTGTCCACCA[-/C]CTGCTGATTCCCATT | 7088 |
rs139340824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612248 | AGAGTATTCCCTACC[C/T]AATTTACAGAGGGCA | 7088 |
rs139361380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648014 | CGGTGGCTTACACCT[A/G]TAATCCCAACACTTT | 7088 |
rs139363416 | snp | A/G | 9.95718e-05 | 0.00705521 | synonymous-codon, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587720 | CAGCTGCCGCCCCTC[A/G]CGCAGGTCCCAGGAC | 7088 |
rs139463875 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81655381 | ATAAAAAAAATAAAG[A/G]AGGCTGGAAAAACCT | 7088 |
rs139572361 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | TLE1 | GRCh38.p7 | 9:81595615 | CGAGATCAGGAGATC[A/G]AGACCATCCTGGCTA | 7088 |
rs139610627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81605058 | GAGCATGCCTGGCAT[C/T]GCACACAAAGCCTGA | 7088 |
rs139641324 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81636688 | GACCAAACATACTCC[A/G]GTAATATTTAGATAC | 7088 |
rs139643002 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81680404 | CTATTCCCAACTCCC[A/C]CTGTTGGATCCTGCC | 7088 |
rs139673974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81601799 | CACTACTTAATAATT[C/T]GAAAATGCGAACAAG | 7088 |
rs139674150 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638923 | CGCCACCACACCAGC[C/G/T]GATACATGCATTTTT | 7088 |
rs139678120 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81685720 | ATGACATTTCATAAT[A/G]CTGTAAAGAGAAAAA | 7088 |
rs139717126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676729 | TCCCAAGACCCTGAA[A/G]ACAATTTACATCTGC | 7088 |
rs139765819 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TLE1 | GRCh38.p7 | 9:81598813 | AAGTGAAATCCATAG[C/T]TTTCCCCTAAGCCAG | 7088 |
rs139797791 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81595376 | TCTATTCATGTCCTA[C/T]AAGAATTCTAGGCTT | 7088 |
rs139803614 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | TLE1 | GRCh38.p7 | 9:81631858 | CTGCAATCCCAGCAC[A/G]TTGGGAGGCTGAGGC | 7088 |
rs139834442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81585403 | TGCATCCAGCTGCTC[A/G]GAGAACATTTTTTCC | 7088 |
rs139863507 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81622950 | CACCAAAAACAGACC[A/G]CTTCCTTTTACTCTT | 7088 |
rs139884683 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81620201 | CCCACAAAGTCAGCC[A/C]TGCATTTTCATATTC | 7088 |
rs139904497 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81683935 | TCATCCCGCCACATA[A/T]CCTACAGGAACCCAG | 7088 |
rs139931738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81658946 | ATGGAGTCTTGCTCT[A/G]TCACCAGGCTGGAGT | 7088 |
rs140076643 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | TLE1 | GRCh38.p7 | 9:81608446 | TGGAGCCTAGGAGGT[C/G]GAGGCTGCAGTGAGC | 7088 |
rs140093317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673725 | GGGGCGGCTTCTGGC[A/G]GACCAATTCCTAGGG | 7088 |
rs140094984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588626 | ACAGGGATCTGCTGA[A/G]CACAGATGCTGTGCA | 7088 |
rs140181964 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687707 | CCAAAGGGAAGGGGG[C/G]TCCCCGGCGGCCAGG | 7088 |
rs140190024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81585720 | GAAGGGAAGACGCAA[C/T]GTGAAAAGTGGGGAA | 7088 |
rs140201906 | snp | A/G | 3.38656e-05 | 0.00411481 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611859 | ACTGGCGTAGGCAGC[A/G]CCTGGGCTGGTCAGC | 7088 |
rs140225510 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TLE1 | GRCh38.p7 | 9:81684555 | ACTTGCTTAATGAAA[A/G]TCTTTGAATATAAGG | 7088 |
rs140249255 | in-del | -/TCCCTTTTTTTTT | 0.495782 | 0.0457324 | intron-variant | TLE1 | GRCh38.p7 | 9:81632472 | TTTAAATGTTCAGTA[-/TCCCTTTTTTTTT]TTTTTTTTTTTTACC | 7088 |
rs140286880 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660338 | TAGACAAAGGCTGTT[-/A]CACAAAAAAAAAAAA | 7088 |
rs140342299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589683 | AATAGCAGGACAGAC[A/G]TTATGAGAACTAAGT | 7088 |
rs140350347 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81651368 | ATGAACTCATGCAGG[A/G]GATGGAATGCACGGT | 7088 |
rs140370299 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689822 | CGTCTCCTCGGTCTC[C/T]CTTCCCATCCCGGCC | 7088 |
rs140372152 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TLE1 | GRCh38.p7 | 9:81645577 | GAAACCTCGTCTCTA[C/T]TAAAAATACAAAATT | 7088 |
rs140394769 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586814 | AGAACAAAAATTGTA[C/T]CCTGCTTATGTTGGG | 7088 |
rs140452824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686361 | CTTTCAAAACCTTTG[A/G]TTTTTAAATCCCTGC | 7088 |
rs140495247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603119 | ATGCTGCTCTCTCCA[C/G]CTAGAGGTTCAGCCC | 7088 |
rs140511735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631319 | TTATCCGACACATTC[A/G]GAAATTCAGAAAGAC | 7088 |
rs140602162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673045 | TGGGAGGCTGAGGGA[A/G]GCAGATTACTTGAGG | 7088 |
rs140602459 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | TLE1 | GRCh38.p7 | 9:81627405 | CCAGTCCCACCAAGG[A/C]CCCGATATCCACCTG | 7088 |
rs140676164 | snp | C/T | 0.142609 | 0.225759 | intron-variant | TLE1 | GRCh38.p7 | 9:81632125 | ATAGGAACCCTGGAA[C/T]GGCAAAACAATAAGG | 7088 |
rs140689682 | in-del | -/A/AAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660978 | CACACACACACACAC[-/A/AAA]ATTTAGCCTGGCGTG | 7088 |
rs140693935 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81673936 | CCATCTGGTGGTCCA[C/T]CCTTTATTCTCTCCA | 7088 |
rs140694894 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81630046 | ACAGATAAAAATCCA[C/T]ACACACCCACATTCC | 7088 |
rs140791900 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81645310 | AGAGGTTGCAGTGAG[C/T]GCCAAGATCGCGCCA | 7088 |
rs140842722 | snp | A/G | 0.000131781 | 0.00811621 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593088 | GTCCCAGACCTTGAC[A/G]CAGCCCTTCCCGCCT | 7088 |
rs140900350 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590560 | AAGTTTGGAGTCTGT[A/G]TGTGGGCTGAAGAAT | 7088 |
rs140915503 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660978 | ACACACACACACACA[-/C]ATTTAGCCTGGCGTG | 7088 |
rs140927509 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690704 | ACTACGAGTCTGTTT[C/G]CAATTCCTGGGAACA | 7088 |
rs140929076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615378 | CATTTGTCAACTGGG[A/G]AGTTTCAGAGAGCTG | 7088 |
rs140937584 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TLE1 | GRCh38.p7 | 9:81599211 | ACTGTTTAGAGATGA[A/G]GGAAGGTGGCACAGG | 7088 |
rs140946387 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81621119 | GGTGTTCCTCGCCAA[C/T]AGCACTGAAATTTAA | 7088 |
rs141015984 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81655237 | GGCGTGATGGTGGGC[A/G]CCTGTAATACCAGCT | 7088 |
rs141016386 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TLE1 | GRCh38.p7 | 9:81612625 | ACTATAGTCTGCAAG[A/G]AGCACGGTTGGGCCA | 7088 |
rs141052580 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81625294 | TTACATCTAACTTGC[A/C]CTAATAGGATGACAG | 7088 |
rs141055926 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | TLE1 | GRCh38.p7 | 9:81649166 | TATCAAATACCTAAG[A/C]AGCTTATTTTTCTTA | 7088 |
rs141074482 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81663461 | TGCAAAGCAACGCAG[C/G]TGCTGAAAGGCCATA | 7088 |
rs141074900 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81614785 | TGGGGCCTCCTTTGT[A/G]CATCACTGATCTGAC | 7088 |
rs141091966 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81637100 | AGGTGGGTCATGCCT[A/G]TAATCCCAGCACTTT | 7088 |
rs141139443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657524 | AATGGCATCAAAGTA[A/G]ACTTGAACATGGTCG | 7088 |
rs141148053 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | TLE1 | GRCh38.p7 | 9:81644925 | TTTGAACCCGGGAAG[C/T]GGAGGTTGCAGTGAG | 7088 |
rs141150086 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | TLE1 | GRCh38.p7 | 9:81606986 | CCCAGCACTTTGGGA[G/T]GCCATGGCAAGAGGA | 7088 |
rs141165504 | snp | C/T | 0.031825 | 0.122064 | intron-variant | TLE1 | GRCh38.p7 | 9:81652522 | TCTGGCTGTAAATTT[C/T]GGCTTGGAATGGTAG | 7088 |
rs141182489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81604240 | TAGGCTGTGAGCTCC[C/T]GGTGGGGTCCCCTAT | 7088 |
rs141188720 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81642208 | TCTCAAAAAGTTAAA[A/G]ATAGAACTACTTTCT | 7088 |
rs141302883 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81607585 | TCCACCAAAGGTTCA[C/T]TGGTTACTGGTATTA | 7088 |
rs141306394 | in-del | -/GAGAAC | | | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583255 | GGAGAGAGAGAGAGA[-/GAGAAC]GAACGAAAGAAAGAG | 7088 |
rs141359420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81669280 | CAAATGGCTTGACCT[C/T]AGACCAATTTTCATC | 7088 |
rs141391384 | snp | C/T | 0.000153988 | 0.00877328 | missense | TLE1 | GRCh38.p7 | 9:81616657 | TTACCTCATTAGACA[C/T]ATCCACAACTAAGTT | 7088 |
rs141414804 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81600276 | CAAGAAATATACACA[C/T]TACATTTATATCCCA | 7088 |
rs141453237 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81633184 | TAAGAAAAAGAAATT[C/T]TAAAGGAAAAAAAGT | 7088 |
rs141490340 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81647921 | GCCATTGTTTACTAT[C/T]AATATTTTTAAAAAT | 7088 |
rs141524882 | snp | A/G | 4.49661e-05 | 0.00474141 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687408 | GATAGTGAACTTGAA[A/G]GGCTGGCCTGCAGCC | 7088 |
rs141525822 | snp | C/T | 1.70676e-05 | 0.00292122 | missense | TLE1 | GRCh38.p7 | 9:81611885 | TCAGCTCGCCGTTCA[C/T]GCCAGCGTGGGGGAC | 7088 |
rs141533251 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TLE1 | GRCh38.p7 | 9:81597023 | CACAGGCAAATCAAG[C/T]GCCCAAACTTTGCTG | 7088 |
rs141544661 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81630355 | CATTCAAGACATTTG[C/T]AGACATACATAACAA | 7088 |
rs141546510 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81595452 | TCAGAATCAGGCTCC[A/G]TACTCTGGGTCCAAA | 7088 |
rs141570146 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81628768 | AATCTGTTAACTAAG[C/T]ATGTGACCGGATGCA | 7088 |
rs141570179 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593433 | TGAAGCATTTACTGC[C/T]GGTGCAAATTTAAAA | 7088 |
rs141587262 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81626783 | GACAGGGTGCTAAAA[C/G]CACGATGCCTTCGTC | 7088 |
rs141608977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624983 | AGGGTCAAGTACCCT[A/G]TACATAAAGGGAGAA | 7088 |
rs141647936 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81652227 | ACCCCGATGATGGCA[C/T]TCAATTCTGCCATGG | 7088 |
rs141659001 | snp | A/G | 0.0429429 | 0.140098 | intron-variant | TLE1 | GRCh38.p7 | 9:81634059 | GCACTGTAAGAGTAT[A/G]AGGACAAAGTCCTAA | 7088 |
rs141691769 | in-del | -/T | 0.0596104 | 0.162024 | intron-variant | TLE1 | GRCh38.p7 | 9:81664985 | TTAGCACCTGCCAGG[-/T]GCTCTGACACCCTCT | 7088 |
rs141808128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678846 | CTCCATCTCAAAGAA[A/G]AAAAAAATTAGGGGC | 7088 |
rs141837451 | in-del | -/TTAGA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663348 | CCAAGATCATAGAGC[-/TTAGA]AAGAAGCCACATATT | 7088 |
rs141875057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81585093 | ATCCTCACTGTAGAG[C/T]AGAGTGTAACTAAGT | 7088 |
rs141894076 | in-del | -/C | 0.0644693 | 0.167566 | intron-variant | TLE1 | GRCh38.p7 | 9:81685579 | AAAATAGCATACAAA[-/C]CCCCACCCCTAGAGC | 7088 |
rs141897276 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TLE1 | GRCh38.p7 | 9:81683428 | CTCTCTACAATATAA[C/T]GAGCACTTAGGCCAT | 7088 |
rs141898955 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81643068 | TGGCGGCTGCCTTGC[A/G]GGGTAGGGGAAAATG | 7088 |
rs141902665 | snp | A/C/T | 0.000132112 | 0.00812651 | intron-variant | TLE1 | GRCh38.p7 | 9:81584344 | GTGTTTAATGTGGAA[A/C/T]AACGGTACTCAGAGG | 7088 |
rs141904487 | in-del | -/CT | 0.00795532 | 0.062565 | intron-variant | TLE1 | GRCh38.p7 | 9:81632233 | TGTCCCCCCAATCCC[-/CT]CTCAACATTTTCCAG | 7088 |
rs141940014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81682974 | ATCAGGAAGTGTTGA[C/T]ACAACCTAAACACGG | 7088 |
rs141958003 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677563 | GAGCGAGACTCCATC[A/T]CAAAAAAAAAAAAAA | 7088 |
rs141959893 | snp | C/T | 0.00200752 | 0.0316185 | missense | TLE1 | GRCh38.p7 | 9:81611849 | TGTTGTGTAAACTGG[C/T]GTAGGCAGCGCCTGG | 7088 |
rs141997116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611675 | GGCTGCTCCTGCCCA[C/T]GCAGCGCAGAGAGGC | 7088 |
rs142008667 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TLE1 | GRCh38.p7 | 9:81679976 | TCAAGATGATTTATT[C/T]AAATATTTACTAAAG | 7088 |
rs142030700 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81618860 | GTACCGGACCCTTCT[A/G]CAAATATAAACCTTC | 7088 |
rs142052366 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81610015 | CTCTCCAGAAATAAC[A/T]AAGGAGATCACCCCC | 7088 |
rs142070021 | in-del | -/ACCCC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591872 | TGTGTTTCCAAAACA[-/ACCCC]CCGCCACTCTGCTTT | 7088 |
rs142098069 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | TLE1 | GRCh38.p7 | 9:81613278 | GGCCCTACGTACATT[G/T]CATATTTGTAGGGCA | 7088 |
rs142108700 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TLE1 | GRCh38.p7 | 9:81674665 | CAAGTTTCATTGAGG[A/G]GTCAGAACAAAGAGA | 7088 |
rs142117661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81649994 | ATCCAAAAATTACAA[C/T]GATAAAAACCGCACA | 7088 |
rs142153989 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81661595 | TTCTTTGAACCAAGC[A/G]GGAAGCCAAGATAAA | 7088 |
rs142159307 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | TLE1 | GRCh38.p7 | 9:81598087 | GCCTACGGACTTGGC[A/C]CTCTGGATGTGAAAT | 7088 |
rs142189746 | snp | C/T | 0.000148885 | 0.00862671 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616120 | GGCAGGGCTTGCTCG[C/T]GGAGAAGAAGGGTCC | 7088 |
rs142194356 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645754 | TCCAAAAAAATAAAA[A/T]AAAATAAAATAAAAT | 7088 |
rs142200191 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610749 | CATACCTGCCCCCCC[-/C]TCCCACCCCCAGTTA | 7088 |
rs142213189 | snp | A/G/T | 0.000300421 | 0.0122523 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634250 | GGTGAGGCGTAAGGG[A/G/T]AACTGGGGGTCCGTG | 7088 |
rs142263774 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TLE1 | GRCh38.p7 | 9:81603095 | CGTGAAGTCACCGGG[C/T]CTTTGCACATGCTGC | 7088 |
rs142295842 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81626134 | AAAATAAAGCACATT[A/G]TTCAAATGGATTTCT | 7088 |
rs142337535 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81622904 | ACGCAGCTGCCGGAC[A/G]CCCGGCAGGCTTTCC | 7088 |
rs142337941 | snp | G/T | 0.000790391 | 0.0198638 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81610237 | TTTCCCCCCAGGGAT[G/T]CCTGCCAGGTTTGGA | 7088 |
rs142353357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662532 | GAACCCTGTCTCTAC[C/T]AAAAATACAAAAAAA | 7088 |
rs142388849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81659773 | CACTTAAACCACTGG[A/G]TCCCAACCAGGTCTC | 7088 |
rs142424344 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81596094 | TGCTTATCATAGAGT[G/T]AAATGTTCCAGATTA | 7088 |
rs142458504 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584110 | GTTTGTAATTTTTTT[-/T]CTCTTTTAAAGTTAC | 7088 |
rs142459749 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81680681 | TTGCACCTCGGAATC[C/T]AGGCTCTAAATGCAG | 7088 |
rs142563667 | snp | A/G/T | 5.02781e-05 | 0.00501367 | synonymous-codon, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81685691 | CTGTTTGTGCATTTC[A/G/T]ATGTTTAATCCATAT | 7088 |
rs142587320 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81595589 | TCTGGGAGGCCAAGG[C/T]GGGCGGATCACGAGA | 7088 |
rs142607301 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81627248 | AACCTGCTCACAATT[C/G]CAGGTTTTCTAATTA | 7088 |
rs142711358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610968 | CAGCCTCTCCTACAA[C/G]TGCAATATCAGGAAA | 7088 |
rs142750531 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81646315 | GGAGAAACGGACTGC[A/G]AAGACTTCTTTGCAA | 7088 |
rs142767138 | in-del | -/AAAATAAAAT | 0.348574 | 0.229746 | intron-variant | TLE1 | GRCh38.p7 | 9:81645745 | AACTCTGTCTCCAAA[-/AAAATAAAAT]AAAATAAAATAAAAT | 7088 |
rs142777294 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638128 | TACACAGAGACAAAT[A/C]CACCCTCACCAACAG | 7088 |
rs142790799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81659656 | TCCTTACCTATGCCA[A/G]CTCTCCTCACTGATT | 7088 |
rs142797375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634574 | CTCACATCTACACTG[C/T]CACTTTCTGGTATCA | 7088 |
rs142818206 | in-del | -/G | 0.0748431 | 0.178382 | intron-variant | TLE1 | GRCh38.p7 | 9:81643619 | TCTCATTGCAGCCTT[-/G]GAAGTCCCAGACTCA | 7088 |
rs142832978 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643818 | TGGGATTACATGTGT[A/C/G]AGCCACCATGCCTGG | 7088 |
rs142851574 | in-del | -/AC | 0.0341408 | 0.126114 | intron-variant | TLE1 | GRCh38.p7 | 9:81631011 | GTAATTAGGCAGGAA[-/AC]ACAGCATATATACTT | 7088 |
rs142863449 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | TLE1 | GRCh38.p7 | 9:81675796 | ACCTCCAACCCCCTG[A/G]TTCAAGTGATTTTCC | 7088 |
rs142960681 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81608685 | CTCACGCCTGTAATC[A/G]CAACACTTTGGGAGG | 7088 |
rs143065311 | snp | G/T | 1.72068e-05 | 0.00293311 | missense | TLE1 | GRCh38.p7 | 9:81610277 | GGTACTCTCATGTGA[G/T]GGGGAGGATCAAACC | 7088 |
rs143069664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81591656 | TGAAAGATGCAGATA[C/T]GGCTAAAGTTTGCTT | 7088 |
rs143088790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597303 | AGCCAAGTGAAGATA[A/C]GTTGAATTGAGGGCT | 7088 |
rs143129263 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81607395 | ACTGTGCCCACCCAC[C/T]AGCCTTCCACCCTAG | 7088 |
rs143137091 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588474 | CTGACCTCAGAGGCA[C/T]TGGGCAGAGACACAG | 7088 |
rs143149706 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642689 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAATGAAA | 7088 |
rs143160047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621424 | GCAAGGGGGCAATTT[A/G]TTCAGTGATGTGTTA | 7088 |
rs143188345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656079 | TGTACTAGAAGGGGA[A/G]ATGACTGGTAGAGAG | 7088 |
rs143199419 | snp | C/T | 1.64825e-05 | 0.00287071 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590921 | GGCGGGGGCCGAGGA[C/T]GTCAGCTCCGCCTTG | 7088 |
rs143205044 | snp | C/T | 0.000469933 | 0.0153214 | intron-variant | TLE1 | GRCh38.p7 | 9:81593002 | GAGAAATTGCCCTTG[C/T]GCACCAGTTCCTGTT | 7088 |
rs143208469 | snp | A/C/G | 0.000973901 | 0.0220462 | missense, synonymous-codon | TLE1 | GRCh38.p7 | 9:81585599 | CACCTCCACATTGCT[A/C/G]CTCTCCATGCCCACT | 7088 |
rs143226940 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TLE1 | GRCh38.p7 | 9:81618431 | CCCAGAGCACTACAC[A/G]TGAGAGACCCAATTT | 7088 |
rs143294749 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | TLE1 | GRCh38.p7 | 9:81596336 | ATCAGTCACAGGGGG[A/C]CTCGCAGGAAGCTGG | 7088 |
rs143297940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687171 | GAAGAGGCGGCCCGG[A/G]AAGAACCAGGAAAGG | 7088 |
rs143311552 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81623022 | TTCTTCCAGCCCTGA[C/T]GCTGCTTTCATTGTT | 7088 |
rs143340630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629709 | CTCCTAGGCTACAAA[C/T]CTGTACATGTTACTG | 7088 |
rs143365960 | snp | C/T | 0.000707516 | 0.0187951 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634187 | ACAGCGCAAGAAGGC[C/T]GGCACTGCCCCCGAG | 7088 |
rs143371277 | snp | A/C/T | 0.0126979 | 0.078662 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689169 | CTTTCCTTCCTTCAC[A/C/T]TTCGTGTGCTTCTCC | 7088 |
rs143412325 | in-del | -/GGG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653175 | ATGGTGGAAGAGGCT[-/GGG]GTTACAACAATAATG | 7088 |
rs143463211 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81674539 | TTCCATACACACAAA[G/T]TTCAAAATCAGAGTC | 7088 |
rs143566694 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81677903 | GTACAGTGGTGTATA[C/T]CTAGCATACTTAATT | 7088 |
rs143570155 | snp | A/C/G | 0.00795819 | 0.0626103 | intron-variant | TLE1 | GRCh38.p7 | 9:81610405 | AAGCAACATAAATGG[A/C/G]AACAGTAACATGGCC | 7088 |
rs143574563 | in-del | -/TGTCATCCCGCC/TGTGTCATCCCGCC | 0.352938 | 0.227824 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587922 | GTGTGTGTGTGTGTG[-/TGTCATCCCGCC/TGTGTCATCCCGCC]TGTGTGTGTGTGTGT | 7088 |
rs143607655 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81620771 | ATCAAACCATCCAAA[A/G]CTAGGTGGATTCTTC | 7088 |
rs143610197 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81672626 | GAGCAAAAAGAAAAC[G/T]ACATGCACACACTCC | 7088 |
rs143644802 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81604507 | GGTAGGAAAGAGCCA[C/G]GATTGATGAGTCAAA | 7088 |
rs143702053 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81666116 | CCTTGTTATGGAGTT[C/T]AGAAAGAGCCTGTTC | 7088 |
rs143703180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676581 | GGAAATGCAGGAAGA[C/G]AAAGAAGCAGTGGCC | 7088 |
rs143712659 | in-del | -/TT | 0.0193772 | 0.0965046 | intron-variant | TLE1 | GRCh38.p7 | 9:81609750 | CCCTTCAAATAACTC[-/TT]GTTTCCACCAAAATA | 7088 |
rs143717216 | snp | A/G | 7.03235e-05 | 0.00592932 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611826 | TGCGGCGCTCATCTG[A/G]GGCGACATGTTGTGT | 7088 |
rs143722394 | snp | C/T | 0.031825 | 0.122064 | intron-variant | TLE1 | GRCh38.p7 | 9:81653399 | CTTGAGTCAGTTTCA[C/T]AGATTACTCATATAA | 7088 |
rs143742695 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81608556 | ATGCAAGTGACGTAC[C/T]GATAAAAGCTGAAAG | 7088 |
rs143750833 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81600014 | AAATGAGGAAGTATT[A/C]CAGCCAAAGTCAACA | 7088 |
rs143929053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81594399 | GACATGGATGAAACT[A/G]GAAACCATCATTCCC | 7088 |
rs143936962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656547 | ATCATCCAAGGATAA[A/G]CATGGGTAACATATT | 7088 |
rs143943648 | snp | A/C | 0.0134861 | 0.0810011 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688328 | CGAGGAAAATTAAGC[A/C]GGAAAGCCAAGCAGA | 7088 |
rs143965362 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81597670 | CTACAGATCAGGATC[A/G]CTTCTGCTTCTGAAG | 7088 |
rs143975109 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TLE1 | GRCh38.p7 | 9:81654618 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACTGCA | 7088 |
rs143997606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631200 | TCAAGAACTGCTTCA[C/T]ACTTCTTGAAGGGGA | 7088 |
rs144027618 | snp | A/G | 0.00681387 | 0.0579699 | missense | TLE1 | GRCh38.p7 | 9:81613457 | GCGCTGGTGCCCGGC[A/G]TTGGCATGTCGCTCC | 7088 |
rs144048030 | snp | C/T | 0.000626649 | 0.0176899 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590954 | GCGCGGGGTTGGAGC[C/T]GCCAGGTCCCAAATG | 7088 |
rs144063743 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | TLE1 | GRCh38.p7 | 9:81648141 | GCTGGGTATGGCGGT[A/G]CATGCCTGTAATCCC | 7088 |
rs144142208 | snp | C/T | | | missense | TLE1 | GRCh38.p7 | 9:81584465 | GGAATATGCTGGCTC[C/T]ATAGGGGGTCCGCCA | 7088 |
rs144200739 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81684850 | TGCCATTAATGCTTT[C/G]TTTGGCAGACAATGA | 7088 |
rs144204086 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TLE1 | GRCh38.p7 | 9:81635921 | TCCCAACACTTTGGA[A/G]GCCAAGGCAGGAAGA | 7088 |
rs144241423 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81605415 | TTGTATTGTATGTTA[C/T]AAATGTACCTATCTT | 7088 |
rs144250308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646410 | CGTCACTAAATACAA[A/G]TTAGTAGAGCTAGAA | 7088 |
rs144257500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676311 | AAGCAGACTGCAACC[C/T]AGTCGGAGCAAGGAA | 7088 |
rs144267549 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588144 | AAATTCTTTCCAGGT[C/T]TGGAAAAGTGTTTAA | 7088 |
rs144335336 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81640283 | AAAATAAAAATACTA[C/T]TCAACATTCAATCAC | 7088 |
rs144336963 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81603427 | GAGAGATCCAGGAAA[C/G]ACTTTCTGACCTCTC | 7088 |
rs144402543 | snp | A/G/T | 1.65102e-05 | 0.00287312 | missense, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587733 | TCGCGCAGGTCCCAG[A/G/T]ACCTGACTGTGTTGT | 7088 |
rs144402804 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81622395 | CTGTCATCAGCACTG[A/C]GCATCCAAGCCACAG | 7088 |
rs144490089 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631526 | CACTCACTCCTCCTC[A/G/T]ATTCTCTGGGAAAGG | 7088 |
rs144506886 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81626787 | GGGTGCTAAAACCAC[A/G]ATGCCTTCGTCACCA | 7088 |
rs144524725 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81665780 | AAGCAACTCTATTCA[C/T]TGGTTCTCCTTCCTG | 7088 |
rs144529346 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81627452 | GTAAACAGACACCTC[C/T]ACCTGGTACAGGCTC | 7088 |
rs144566392 | in-del | -/AC | 0.0422008 | 0.138995 | intron-variant | TLE1 | GRCh38.p7 | 9:81653802 | ATTGTCACCATTTCT[-/AC]AGTGTGCCCTCAGAT | 7088 |
rs144595528 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81624538 | TTCAAATATTTATTT[A/G]CCAAATAAATATTTA | 7088 |
rs144598606 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81670865 | AAGCCATACTTAATA[A/C/G]ATTAGTCAAGAAATA | 7088 |
rs144617695 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81667618 | CAGTGCCACATAATG[A/G]CTCCAATTTTGATAT | 7088 |
rs144618505 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81664950 | GAAGCACTGCCATCT[A/C]TTTCAGCAGCATCTA | 7088 |
rs144653229 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | TLE1 | GRCh38.p7 | 9:81673121 | CTACTAAAAATACAA[A/G]AATCAGCTGGGCATG | 7088 |
rs144683885 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81662562 | AATTAGCAGGGCATG[G/T]TGATGCATGCCTGTA | 7088 |
rs144811697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644557 | TAGCAGCCAGAGGTT[A/C]GGGGAGGAGACATGA | 7088 |
rs144840812 | snp | C/G | 0.0126979 | 0.078662 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583920 | CAGAAAGAAAGAATG[C/G]GCTGTCATGTGAGTC | 7088 |
rs144841339 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81594756 | CACCATGAGTACTAA[C/T]ACAGAGCTTAAATTT | 7088 |
rs144850818 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TLE1 | GRCh38.p7 | 9:81657285 | TTTTTTTGCTGTATA[A/G]AACTTTAAGTCTTTA | 7088 |
rs144879360 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81637281 | GAGAATCGCTTGAAC[C/T]TGGAAAGCAGAGGCT | 7088 |
rs144887114 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81614836 | ATGCTCTATGACATG[C/T]CCCGATATTAAGGAT | 7088 |
rs144895816 | in-del | -/C | 0.0966517 | 0.197444 | intron-variant | TLE1 | GRCh38.p7 | 9:81669613 | TTACACCTCCACCCT[-/C]CCCCCCCACACCAAA | 7088 |
rs144903380 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TLE1 | GRCh38.p7 | 9:81682506 | TATAGCATGGCTTCA[C/T]CAGCATGCTGAAAAG | 7088 |
rs144908120 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588948 | GGGAAGGAAAAAGCA[C/T]CACTACTGCCCTAAA | 7088 |
rs144916158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649628 | ATGCAGACTAAGAGC[A/G]TGGCCTCTCCCATTG | 7088 |
rs145004711 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TLE1 | GRCh38.p7 | 9:81682065 | AGCCTGCGAACATGG[A/G]TGAAACCCTCTCTCT | 7088 |
rs145005093 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81649357 | TCTCCTCGAAGAGCA[C/T]CCACAGGCCCAAGAC | 7088 |
rs145015171 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81592483 | AAAGCATTCTCACTG[C/G]TCTCTTTCGTTGATG | 7088 |
rs145094903 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | TLE1 | GRCh38.p7 | 9:81644982 | CTCCAGCCTGGGTGA[C/T]AGAGTGAGACACTGT | 7088 |
rs145104429 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | TLE1 | GRCh38.p7 | 9:81623722 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAATGAGC | 7088 |
rs145128253 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81669499 | TCCAGTCTGCAAGCA[C/G]TACTGTAAAGTAGAA | 7088 |
rs145145560 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81603859 | ACACAAAAATTAGCC[A/G]GACATGGCGGTGTAC | 7088 |
rs145165959 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TLE1 | GRCh38.p7 | 9:81600866 | AAGTTAGAGGAGGAG[C/T]AAGTGTGCCCTTCAC | 7088 |
rs145175462 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | TLE1 | GRCh38.p7 | 9:81663832 | GGGTTTCACCATGTC[A/G]GCAGGATGGTCTCGA | 7088 |
rs145205668 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639768 | TTTGTATTTTTAGTA[A/G]AGATGGGGTTTTGCC | 7088 |
rs145239484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629260 | TCAAGCAGATAAAAA[C/T]AGCATTCCCTTCAGC | 7088 |
rs145243179 | in-del | -/G | 0.0456336 | 0.143994 | intron-variant | TLE1 | GRCh38.p7 | 9:81673709 | AGGTTGACACGGGGA[-/G]GGGGCGGCTTCTGGC | 7088 |
rs145271989 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81601872 | TCCTGGACCTGTCTC[C/T]CACCTATTCAAGGCA | 7088 |
rs145274557 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610952 | TTTGCCCGCCACTGC[A/C]CAGCCTCTCCTACAA | 7088 |
rs145280231 | snp | C/T | 3.3006e-05 | 0.00406226 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685863 | CTGCATTTCTGTCTT[C/T]TCACTTGCCAGTTTC | 7088 |
rs145301885 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TLE1 | GRCh38.p7 | 9:81662462 | CACTTTGCGGGGGCC[A/G]AGGTGGGTGGATCAC | 7088 |
rs145319148 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81598982 | CAAGCAATTGCTTCA[A/G]TTTAATGACCAGTAA | 7088 |
rs145321756 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81668563 | ACAATCCACAGAGGA[A/C]TCTAAGTAAGAGAAA | 7088 |
rs145325305 | in-del | -/A | 0.0256215 | 0.110247 | intron-variant | TLE1 | GRCh38.p7 | 9:81676211 | ACTACCACTACACAT[-/A]AGGAGTACCCAAAAC | 7088 |
rs145436725 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81606798 | AAAACCATATATATA[G/T]ATATAGAGAGAGAGG | 7088 |
rs145445525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674056 | TTTCAAATGGCACAA[A/G]TAACGGTGGCTGCAT | 7088 |
rs145492796 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652019 | GTCATCTTCCTTATG[C/T]TAAGCCCTCTTCCTC | 7088 |
rs145505174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81655661 | CAATGCTTACTAAAT[A/G]CCACCTATATTACTG | 7088 |
rs145529259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589920 | ACCGGGCCCGGCTCA[A/G]TGACACTTCATGGAT | 7088 |
rs145545216 | snp | A/G | 6.60142e-05 | 0.0057448 | synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81654013 | TTGTGCACAAATCGT[A/G]TTCAATCTCTTGGCG | 7088 |
rs145570684 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586879 | ACAAAATGTTAACAG[G/T]AATATGAAATTTAGA | 7088 |
rs145608688 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81659425 | TGCTTATAAACTTTC[C/G]CTGTGCCTAGATTTT | 7088 |
rs145614590 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588694 | AGCCCCAGCAGGGAC[A/G]GTGACTGGTGGACTC | 7088 |
rs145632780 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686761 | GGCTGAGATGGATAT[A/G]AATGTGACTCCACTC | 7088 |
rs145652721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81682996 | TAAACACGGGCTGTG[A/G]GCACCACACCAGGAA | 7088 |
rs145673265 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644757 | CCAGCACTTTGGGAG[A/G/T]CAGAGACAGGTGAAT | 7088 |
rs145695762 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585795 | GGAGGTCCACAGGGC[A/G]AGTGATCTAACGCAG | 7088 |
rs145786238 | in-del | -/AAA/CAA | 0.0115144 | 0.0749975 | | | GRCh38.p7 | 9:81618042 | AACAACAACAACAAC[-/AAA/CAA]AAAAAATTCAATGAT | 7088 |
rs145792700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81608560 | AAGTGACGTACTGAT[A/G]AAAGCTGAAAGCAAC | 7088 |
rs145806488 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81637752 | TTCTAGGAAATGTGG[C/T]CATTCCACCTCATAT | 7088 |
rs145863296 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81632796 | CTTATGTCTAAAATA[G/T]ATATAAGATCAAGTT | 7088 |
rs145897600 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81630150 | AGAAAAAAAAAAACA[C/G]TAAGGAGTTCGTCTT | 7088 |
rs145913365 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TLE1 | GRCh38.p7 | 9:81674953 | TGAGTCCAGGAATTC[A/G]AGACCATCCTGGACA | 7088 |
rs145936635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626349 | TAGGTAACGACGCAC[C/T]CCATCACATCTGTGT | 7088 |
rs145974888 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TLE1 | GRCh38.p7 | 9:81661138 | AAAAATAAAAATAAA[C/T]AAAAATAAATAAAAA | 7088 |
rs145985950 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TLE1 | GRCh38.p7 | 9:81658616 | CCCCAGAAAAGGCGC[C/T]GACGTCCTCTGAAAT | 7088 |
rs146070461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81608367 | ATAAATTTAAAAATT[C/G]GCCAGGTATGGTGAC | 7088 |
rs146097247 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81644025 | CAGCCATCAGGAAAA[C/T]GCAAATCAAAAACGG | 7088 |
rs146109160 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81641309 | CAAGGACACTACTGC[A/C]GGAGTTATCGCAAAA | 7088 |
rs146168410 | snp | C/T | 0.00273703 | 0.036892 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611922 | AAAAGGAGCAGGATA[C/T]GGGCCGGGCACTGCC | 7088 |
rs146181317 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | TLE1 | GRCh38.p7 | 9:81597376 | AAAGGGAGGAAGACG[A/C]AGGGTGGGGATCAGG | 7088 |
rs146192361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81595546 | AATTGAGGCTGGGCG[C/T]GGTGGCTCACGCCTG | 7088 |
rs146196744 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81657815 | TTACTTAAAATACCT[A/G]ATACAATGTAAATCC | 7088 |
rs146295477 | snp | C/T | 1.64863e-05 | 0.00287104 | missense | TLE1 | GRCh38.p7 | 9:81584467 | AATATGCTGGCTCCA[C/T]AGGGGGTCCGCCAAG | 7088 |
rs146298631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643277 | GTTTCGCTCTCGTTG[C/T]CCAGGCTGGAGTACA | 7088 |
rs146310230 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | TLE1 | GRCh38.p7 | 9:81639584 | AAAGTTGTTTTTTTT[G/T]TTTGTTTTTTTTTTT | 7088 |
rs146337065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680091 | ACGCACGAGGTGCTG[A/G]GTTCTGCGGGTGTAT | 7088 |
rs146347390 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81676635 | GGGGTAGACACAGCA[A/G]GCTATGAGGGACAAA | 7088 |
rs146392581 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677564 | AGCGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 7088 |
rs146458470 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TLE1 | GRCh38.p7 | 9:81620102 | ATTGAGAACGCAAAG[A/G]TGGTGAGATCAGAGC | 7088 |
rs146461149 | snp | A/C | 3.42601e-05 | 0.0041387 | missense | TLE1 | GRCh38.p7 | 9:81610242 | CCCCAGGGATTCCTG[A/C]CAGGTTTGGAGGAAT | 7088 |
rs146472651 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81617482 | GCGGGCAGGTGGATC[A/G]CTTGAGGCCAGGAGT | 7088 |
rs146476154 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81621213 | GCAGGAACAAGGACT[A/C]ATCTTTTCCACAAAT | 7088 |
rs146499396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655955 | AAGATGATCTGAATT[A/C]ACTAAGCAAAGTCTT | 7088 |
rs146511815 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81652502 | AAACAACACCAGTCA[A/C/G]TACTTCTGGCTGTAA | 7088 |
rs146555451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618068 | ATGATGCGATCATCC[C/G]TACATCAAGTTTGAG | 7088 |
rs146556482 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81659821 | CACCAATCTACTTGA[A/C/G]AGTTTCATCAAAATC | 7088 |
rs146582986 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | TLE1 | GRCh38.p7 | 9:81605632 | TTCAAGATGGATTAA[A/C]GATTTAAATATTAGA | 7088 |
rs146619787 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | TLE1 | GRCh38.p7 | 9:81636981 | GTACTCCAGCCTGGA[C/T]GACAGAGGGAGACTC | 7088 |
rs146630385 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81633145 | AAGTTTTGTAAAAAG[A/T]CAAGAGCAGAGCGAA | 7088 |
rs146691736 | snp | C/T | 1.64846e-05 | 0.0028709 | missense | TLE1 | GRCh38.p7 | 9:81590940 | AGCTCCGCCTTGATG[C/T]GCGGGGTTGGAGCCG | 7088 |
rs146713435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589616 | CTGTGTGACCTGAAG[C/T]CAGTAACTTACCCTC | 7088 |
rs146729674 | in-del | -/C | 0.0752113 | 0.178743 | intron-variant | TLE1 | GRCh38.p7 | 9:81684807 | TGAAAAAGTGAATGT[-/C]CAGCGTATCTCCAGA | 7088 |
rs146737801 | snp | C/T | 0.0130921 | 0.0798413 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689184 | CTTCGTGTGCTTCTC[C/T]GCAAAGGGCGCTCCA | 7088 |
rs146748510 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81656644 | CATTTTAATACCAAG[C/G]GGTTTCCGTTACATA | 7088 |
rs146749992 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686337 | AGTTACTCCTACAAT[G/T]GCTGGTCCCTTTCAA | 7088 |
rs146751913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617589 | TGCCTGCAGTCACAG[A/C]TATTCAGGCAGCTGA | 7088 |
rs146794728 | in-del | -/ACAC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607338 | ACTGACCCTGTTAAT[-/ACAC]ACACACACACACACA | 7088 |
rs146821090 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81636685 | TCAGACCAAACATAC[C/T]CCGGTAATATTTAGA | 7088 |
rs146854497 | in-del | -/AAAGAAAG | 0.100231 | 0.200173 | intron-variant | TLE1 | GRCh38.p7 | 9:81642030 | TCCATCTCCAAAAAA[-/AAAGAAAG]AAAGAAAGAAATGTC | 7088 |
rs146859171 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81673886 | GGAGTGTGTACCTGT[A/G]TCTGCAGGCTGCATG | 7088 |
rs146866389 | in-del | -/AT | 0.0410537 | 0.137264 | intron-variant | TLE1 | GRCh38.p7 | 9:81634367 | GTGACAGTGATGGCG[-/AT]ATGGAGGCGGCATCC | 7088 |
rs146871375 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81669919 | GCCCCCACAGTATAT[C/G]AATGTCAAACAACAT | 7088 |
rs146925262 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | TLE1 | GRCh38.p7 | 9:81609275 | TTTTTAGTAGAGACG[C/G]GGTTTCGCCACATTG | 7088 |
rs146948157 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81607014 | GGATCACTTGAGCCC[A/T]GGAGTTTGAAACCAG | 7088 |
rs146958161 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81604242 | GGCTGTGAGCTCCCG[A/G]TGGGGTCCCCTATGC | 7088 |
rs146981408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638242 | TCTGCAAAAGGACAC[C/T]ATCCCTTGCCCCCAG | 7088 |
rs147012155 | snp | A/G | 3.29587e-05 | 0.00405934 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616679 | AACTAAGTTGTCATC[A/G]CTTTTGTCACCATCA | 7088 |
rs147053908 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81593444 | CTGCTGGTGCAAATT[G/T]AAAATAATTAATAGC | 7088 |
rs147078340 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691438 | TCTTAAACAAGTTGG[A/G]CATTGTAGCTTTGTG | 7088 |
rs147086301 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81622081 | CCCTCCAACCCAGAC[A/C]CCCAGCTGACAAGGC | 7088 |
rs147201560 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81604726 | GTCCCTCCTGCCCCA[A/G]CTGAACTCTTCTGGC | 7088 |
rs147205271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672628 | GCAAAAAGAAAACTA[C/T]ATGCACACACTCCCC | 7088 |
rs147224517 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81602735 | AATAAAGAATACACT[A/G]ACAGCAATCTGATGA | 7088 |
rs147329787 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | TLE1 | GRCh38.p7 | 9:81648188 | GAGGCAGGAGAATCA[C/G]TGGAACCCTGGGAGG | 7088 |
rs147339622 | snp | A/G | 0.0337553 | 0.125452 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687957 | GGGATATGGCTGCAG[A/G]AGAGAAACCCCAGCC | 7088 |
rs147402757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81601797 | AACACTACTTAATAA[G/T]TCGAAAATGCGAACA | 7088 |
rs147412508 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634895 | ACTATCACTAAGGAA[C/T]AGAATTTGGAAAGGA | 7088 |
rs147412812 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81598741 | TAAGGGGGAAAGGCA[C/G]TCTCTAGACAGCTGA | 7088 |
rs147436036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81631712 | ATAGATTTAAAACGC[A/G]TAACAGCCTAAAGGG | 7088 |
rs147482247 | in-del | -/CAT | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81666432 | AGGAAAAGTAGACTA[-/CAT]CATCATCATCATCAC | 7088 |
rs147484928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81591713 | TCAAAGATTAAAGAA[A/G]CTTTAAGCACATGAC | 7088 |
rs147518710 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81618825 | TGAAGTGAGTTTACC[A/G]TAATTTAAATCTTAG | 7088 |
rs147523347 | snp | A/G | 0.0180743 | 0.0933299 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687396 | CAGGGACTCCGGGAT[A/G]GTGAACTTGAAGGGC | 7088 |
rs147533720 | in-del | -/C | 0.0498117 | 0.149749 | intron-variant | TLE1 | GRCh38.p7 | 9:81675498 | AAACCTAGGCCCCAG[-/C]CAACATGCTAGTTTT | 7088 |
rs147541111 | snp | A/G | 0.000856376 | 0.020675 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616069 | ATCCTTCTTTAGCAG[A/G]CGATTTTTGTCGATT | 7088 |
rs147551154 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81613248 | CATGGCTTTTTCAGA[C/G]ATAGGAAGGAGGGTG | 7088 |
rs147555006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680791 | CAGCTACCCTCTTTG[C/T]ATGACAAGATTATTA | 7088 |
rs147655112 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | TLE1 | GRCh38.p7 | 9:81662483 | GGTGGATCACCTGAG[A/G]TCAGGAGTTCGAGAC | 7088 |
rs147657152 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81599018 | GGGCACCAAGCCTAA[C/T]TAACTTGAGCCTCAT | 7088 |
rs147679909 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81595963 | ATTAGTTTTTCTCTG[C/T]GTACCACAAATCAAG | 7088 |
rs147759580 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81644863 | GCCAGGCATGGTGGT[A/G]TGTGCCTGTAATCCC | 7088 |
rs147761773 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585842 | AACCTTTAGGAAACT[C/G]GAAACATTTGAACCC | 7088 |
rs147782475 | snp | C/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81642161 | GAATGTAAATTGGTA[C/T]AGCCCTGATGCAAAA | 7088 |
rs147782794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684863 | TTCTTTGGCAGACAA[C/T]GACTACTCAATCGAG | 7088 |
rs147792854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81681609 | CCAGTGCTCTCACTC[C/T]GCCCATTCTTCAGCA | 7088 |
rs147865073 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81628118 | AACCCAGAAGTAACT[C/G]CATTGAATGTAATGA | 7088 |
rs147867092 | snp | A/G | 0.000346081 | 0.0131499 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81620489 | TTTCTTGATGTCATT[A/G]GAAAATTCAGGTCCA | 7088 |
rs147888272 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81624566 | TTAATCGAGAATCAG[C/T]TTTTTGATCAACATG | 7088 |
rs147897931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662611 | GCTGAGGTGGTAGAA[C/T]AGCTTGAACCCATGA | 7088 |
rs147941591 | snp | A/G | 0.00604284 | 0.0546343 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585524 | GTAAGCAAATTTCAG[A/G]GACAGCACGCAGCTC | 7088 |
rs148001510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81674599 | CTATCGTTGCTAACA[A/G]TATTTCCCCCAGCAA | 7088 |
rs148060117 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TLE1 | GRCh38.p7 | 9:81678358 | AGCTAGTACTACAGG[C/T]CTGTACCACCAGGCC | 7088 |
rs148064084 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589944 | CATGGATTTCTACAG[C/T]GGAGGTTTGAAGAGA | 7088 |
rs148107690 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TLE1 | GRCh38.p7 | 9:81615017 | ATGGCCAACATGAAA[C/T]CCTGTAATAAGCCAA | 7088 |
rs148132074 | snp | G/T | 0.000411734 | 0.0143422 | missense | TLE1 | GRCh38.p7 | 9:81611838 | CTGGGGCGACATGTT[G/T]TGTAAACTGGCGTAG | 7088 |
rs148142705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663343 | ATTTGTCCAAGATCA[C/T]AGAGCAAGAAGCCAC | 7088 |
rs148176551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81657485 | CATCTTTAACTATGA[C/T]AGCAACTATGTGTTA | 7088 |
rs148195319 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | TLE1 | GRCh38.p7 | 9:81670923 | CTGTTAATCCCAGCA[A/C]TTTGGGAGGCCGAGG | 7088 |
rs148204707 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81604136 | CATGCATTTCTCCTG[C/T]TAATCTATCTTATGT | 7088 |
rs148256748 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81607431 | CAGCTCACAGCTCTG[C/T]TCACCCGCCTTCCCC | 7088 |
rs148266384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81642954 | AGATGTGCAGAACAG[C/T]AGGCTAAGCGAAATA | 7088 |
rs148320340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588422 | TGCATTAGGAAATCT[A/G]GACTCCCAGAGACAA | 7088 |
rs148324186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646582 | AAGAGGCCAACCTCA[C/T]CCTCTTAAACTTCAC | 7088 |
rs148334119 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687252 | GACGCAAGAACTAAG[C/T]ACAGGCGCCGCCGCC | 7088 |
rs148338730 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81596650 | TGAATATCGCTCACA[A/C]CTGAATTCAGAATGA | 7088 |
rs148361137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629838 | CTTAGGGGACCACCA[C/T]CATATATGCAATCCA | 7088 |
rs148393875 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81622813 | TGATGCTGTAAAACT[G/T]ACTCAAAACAAGGCA | 7088 |
rs148445717 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81626796 | AACCACGATGCCTTC[A/G]TCACCACCCTCTCAT | 7088 |
rs148451330 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81652852 | TTGATTGGTTGATCA[C/T]TTGTCTGATCAACCA | 7088 |
rs148456224 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81665833 | TTGCAAATGACAAGC[C/T]TGCCAGGCCCCACTT | 7088 |
rs148509760 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81605408 | TATTCATTTGTATTG[C/T]ATGTTACAAATGTAC | 7088 |
rs148517087 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81584611 | TAATCAAACTAAGAA[C/G]ATTTTTAATATATGA | 7088 |
rs148561185 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81608675 | GGCACGGTGGCTCAC[A/G/T]CCTGTAATCGCAACA | 7088 |
rs148583581 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81644625 | GTGACAAAAATGTTC[C/T]AGAAAAATTTTATAG | 7088 |
rs148585563 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81618854 | AGCTTTGTACCGGAC[C/G]CTTCTGCAAATATAA | 7088 |
rs148605258 | snp | A/G | 3.29625e-05 | 0.00405958 | missense | TLE1 | GRCh38.p7 | 9:81590916 | TAGCAGGCGGGGGCC[A/G]AGGACGTCAGCTCCG | 7088 |
rs148634896 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81649674 | CGGCCCCTGAACAAT[A/G]CTGACAGCTGCTATC | 7088 |
rs148646646 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81661188 | TATATATATGTATTT[A/T]TATATATATATGTAT | 7088 |
rs148656064 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | TLE1 | GRCh38.p7 | 9:81597943 | CTATGCTGTGTTCTG[A/C/T]GGTCAAAGGAAAACA | 7088 |
rs148717810 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | TLE1 | GRCh38.p7 | 9:81636080 | GAGAGCATGGTTCTA[A/C]TTAGAAGCAAAATGG | 7088 |
rs148748610 | in-del | -/TTCTTT | 0.0737376 | 0.17729 | intron-variant | TLE1 | GRCh38.p7 | 9:81632749 | GTCCACTGAATTTCC[-/TTCTTT]TTAAGAGCTTACTGG | 7088 |
rs148776936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81641511 | TGGGCAACCTAAGGA[A/T]TGGGAGAAAATATTT | 7088 |
rs148786586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81680674 | GCTAATCTTGCACCT[C/T]GGAATCTAGGCTCTA | 7088 |
rs148828029 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81674495 | CACCCAAGGTCCCTG[A/G]GGCCAACTGAAAATC | 7088 |
rs148848896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81616993 | AATACTTGGCAGATT[A/G]TAAGAGCTCAGTAAA | 7088 |
rs148873371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677901 | GCGTACAGTGGTGTA[C/T]ATCTAGCATACTTAA | 7088 |
rs148881824 | snp | C/T | 0.00140993 | 0.0265137 | intron-variant | TLE1 | GRCh38.p7 | 9:81610207 | ACAAAACCAAGGTCT[C/T]TGAGGTACTTACGGT | 7088 |
rs148909738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659448 | TAGATTTTTTAATAC[C/T]GTGTAAGGCAACAAC | 7088 |
rs148963644 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81599818 | GAGGGCTTTATTAAC[A/C]ACTAACTTGAAAGTA | 7088 |
rs149014733 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81604055 | GCTGTCTGCTCTGGT[C/G/T]GCTTCTTTGGGTCTT | 7088 |
rs149058551 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589396 | CTGGGTTACAGTGGA[C/T]ACAAAGACATTCAAT | 7088 |
rs149098757 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81682110 | AAAAAAAAAGTTAGC[C/T]GGGCATGGTGGCGGA | 7088 |
rs149120533 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81624149 | CTTAACATTCTAATG[A/T]GACATAATACCTGAC | 7088 |
rs149172710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81629636 | TCATTGTGCAAATAT[C/T]GAATAGTGTGTTTAC | 7088 |
rs149257316 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606774 | GAACTTAAAGTATAA[-/T]TTAAAAAAAAAACCA | 7088 |
rs149281453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665551 | CTGAAGGCTGCTTGG[A/G]CACAGATAGCAACAC | 7088 |
rs149283987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81601453 | TCTGGCATTAAAACA[C/T]AGGGTGAAAGGACCT | 7088 |
rs149346314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639495 | AGTAATTAGGAAATT[C/T]GCTTAAAAGTCAAAA | 7088 |
rs149354775 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81614922 | GTTTGAGGCCAGGTG[C/T]GGTGGCTCACACCTG | 7088 |
rs149364917 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81652916 | GGAATTCCTCTCATT[C/G]TTTTATAGCCTTTTG | 7088 |
rs149418035 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81656874 | AAAGGAATCCCTAGA[A/T]GTGAAACTGCTGGGT | 7088 |
rs149421730 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TLE1 | GRCh38.p7 | 9:81684524 | GTTACAAAAGCAGAA[C/T]TCAACTCTGAAACAC | 7088 |
rs149495671 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81630945 | AAATGCTTAGGTTAC[A/C]ATTAGTGTAGTTTTC | 7088 |
rs149547568 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81635426 | TCTAAGTCTGTTCTC[A/G]TTACACAGTATCATT | 7088 |
rs149557460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676089 | CAAACAGCCAAAATC[A/G]TTGGGCAAAGCTATC | 7088 |
rs149567945 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588098 | ACCCAGAACTTAAAT[A/G]TGCTACTCTGACAAA | 7088 |
rs149577837 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81617985 | AGCCGAGATTGTGCC[A/G]TTGCACTCCAGCCTG | 7088 |
rs149581631 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686942 | ATTTTCTAGTATGGC[A/G]AACAGCGATTTCAAC | 7088 |
rs149612113 | snp | A/G | 0.00190888 | 0.030835 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634116 | GTGGTGCTCTGCATC[A/G]TGGTGCTTCTTGTCA | 7088 |
rs149629055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622327 | CACAGAGGCTGGGTG[C/T]GCTGACCAGTTTTAA | 7088 |
rs149661433 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81616529 | AACTTCTTAATGTAA[A/G]AAGTTGCAAGAGGTC | 7088 |
rs149671487 | in-del | -/AC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652106 | GGTCAACGTTAAGAT[-/AC]ACACACACACACACA | 7088 |
rs149684833 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81655468 | GAGAGGGAACAGAGG[A/G]TACTCTACTTCTAGC | 7088 |
rs149694150 | snp | A/G | 3.30077e-05 | 0.00406236 | missense, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81654011 | ACTTGTGCACAAATC[A/G]TATTCAATCTCTTGG | 7088 |
rs149736779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659252 | TTCTTGATTGGAGTG[C/T]GCTGGCAGGTTAACC | 7088 |
rs149790984 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TLE1 | GRCh38.p7 | 9:81599255 | CTCGCCCATAACCAC[A/G]GCTAGTAAGCGGTAG | 7088 |
rs149800733 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81632039 | AGGTTGCAGTGAGCC[A/G]AGATAGTGCTACTGC | 7088 |
rs149820077 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81644069 | ACACCCATTAGGATG[A/C]GGAGAATAAAAAAGA | 7088 |
rs149828134 | snp | A/G | 0.000234016 | 0.0108145 | intron-variant | TLE1 | GRCh38.p7 | 9:81585475 | ATTTGGGCCATCAAC[A/G]GCCTCCAGTTTCCTT | 7088 |
rs149874403 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588751 | TGGGGGAGGCAGCCA[C/G]AAAAGGCGAGCAAAG | 7088 |
rs149876078 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | TLE1 | GRCh38.p7 | 9:81676975 | GGCATGGTGGCTCAC[A/G]CCTATAATCCCAACA | 7088 |
rs149895059 | snp | A/G | 0.0130921 | 0.0798413 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688324 | CCGCCGAGGAAAATT[A/G]AGCCGGAAAGCCAAG | 7088 |
rs150029733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680490 | AATTTTCAAAATATT[C/G]ATCATGATAACTATG | 7088 |
rs150031587 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, synonymous-codon | TLE1 | GRCh38.p7 | 9:81612365 | GAACTTTCCATTCCC[C/T]GGTACCAATTCCAAA | 7088 |
rs150052634 | snp | A/G | 0.000397627 | 0.0140945 | missense, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587722 | GCTGCCGCCCCTCGC[A/G]CAGGTCCCAGGACCT | 7088 |
rs150116226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610075 | AGCTGCCTATTTATA[C/G]AAAGTGTTAACACTC | 7088 |
rs150138895 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | TLE1 | GRCh38.p7 | 9:81645400 | GTAATAATAATTCAA[G/T]TGTAATTTTAAAATA | 7088 |
rs150161989 | snp | A/G | 0.000461133 | 0.0151774 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593112 | CCCGCCTGTGTACAC[A/G]TGTCTCGTGGGGTTG | 7088 |
rs150186823 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81591586 | AGGCATCTTTCCATC[A/C]AAACCGACACATATG | 7088 |
rs150190756 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81652639 | AGGGGTTCATAAGTT[C/T]ACAGCAATTTTAAAA | 7088 |
rs150201131 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690814 | CTCCTGAGCTGAGCT[C/G]TGTGAAGAGCTAAAT | 7088 |
rs150254210 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TLE1 | GRCh38.p7 | 9:81625664 | AGAGCACCCAGTGGC[A/G]TCAAAAGAAAATGTT | 7088 |
rs150272397 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81637248 | CTGTAATCCCAGCTA[C/T]TTGAAAGGCTGAGGT | 7088 |
rs150329189 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81672134 | ACCCAGATCAGAAGG[C/T]GGCCAACTTTGGAGC | 7088 |
rs150411330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656403 | CAACACTCTGTACAT[G/T]CCTCTTCTCGGAAAT | 7088 |
rs150421441 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645001 | GTGAGACACTGTCTC[-/A]AAAAAAAAAAAAAAA | 7088 |
rs150422613 | snp | C/T | 1.64917e-05 | 0.00287151 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81633362 | CTGTGCCCGGCTCTC[C/T]GTCTGCTCCCGAGGT | 7088 |
rs150448258 | in-del | -/A | 0.297382 | 0.245469 | intron-variant | TLE1 | GRCh38.p7 | 9:81629176 | TTTGTCAAATGACTC[-/A]AAAGTATTTAAAAGC | 7088 |
rs150464016 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81660397 | TTCATGTACATGTAT[A/G]GTTTTATTTTTTTAT | 7088 |
rs150473446 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81597071 | TGGTTCTCTGGCTAC[A/G]TCAACTGCGGTCTTG | 7088 |
rs150483131 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81673999 | CCTCTTTCCTAAACC[A/G]AAAGCAACCTTTTTA | 7088 |
rs150507190 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | TLE1 | GRCh38.p7 | 9:81592125 | GCACTTTGGAAGGCC[A/G]AGGCGGGCGGATCAC | 7088 |
rs150519344 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81601234 | AGTGGGGTGAAAGGG[A/G]GAAGCCCCCGGCCAC | 7088 |
rs150569315 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81627275 | ATTACAGAGCACAAA[C/T]TCAAGTCAAAAAGAG | 7088 |
rs150587012 | in-del | -/A | 0.0640965 | 0.167152 | intron-variant | TLE1 | GRCh38.p7 | 9:81680016 | TTCTTTCTGTTTCTT[-/A]ATAAACACTATTTGG | 7088 |
rs150594466 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TLE1 | GRCh38.p7 | 9:81638781 | AGGTGCACACCACCA[C/T]GCCCAGCTAATTTTT | 7088 |
rs150603973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81679145 | AGATTAAGACTCTAT[C/T]GCCATTAAAAAAATT | 7088 |
rs150655291 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81683831 | GCCACAAATGCCTCA[C/T]TCTGTATAGAAACTC | 7088 |
rs150688751 | snp | A/G | 3.39997e-05 | 0.00412295 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611850 | GTTGTGTAAACTGGC[A/G]TAGGCAGCGCCTGGG | 7088 |
rs150699050 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588722 | CTCAGTTCTGCATGC[C/T]GAGAGGAAGGTGGTG | 7088 |
rs150708946 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81619098 | GGCAATTCAGAATTC[C/T]ACATCAGCAAATCTC | 7088 |
rs150727051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630601 | AATTTGATTTCAAGG[G/T]TATCAAGATCATGAG | 7088 |
rs150783307 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81661765 | CTTAAATCCCCCCCC[C/T]AAAAAAAATGTACAC | 7088 |
rs150798064 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81607740 | AGGCTGGAAGCAGGG[A/G]GGCATTCCCAAATTC | 7088 |
rs150806781 | in-del | -/AG | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81640750 | GCTGTTTACATTCAG[-/AG]TGTTACTGTAATGGT | 7088 |
rs150975417 | snp | C/T | 0.000164943 | 0.00907988 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590957 | CGGGGTTGGAGCCGC[C/T]AGGTCCCAAATGGAC | 7088 |
rs150975770 | snp | A/C | 0.00166498 | 0.0288048 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685818 | AAAGGAAAAAGTCCA[A/C]TCTTTGATACCTACC | 7088 |
rs150980614 | snp | C/G | 0.125182 | 0.216612 | intron-variant | TLE1 | GRCh38.p7 | 9:81595590 | CTGGGAGGCCAAGGC[C/G]GGCGGATCACGAGAT | 7088 |
rs151023920 | snp | C/G/T | 0.000568854 | 0.0168556 | intron-variant | TLE1 | GRCh38.p7 | 9:81620909 | CAGGAATACGAATGG[C/G/T]CTATGAGCAAATCTT | 7088 |
rs151027450 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690516 | AAAGATCGTCCTGTC[C/T]CGTTTGGCGGGAAGG | 7088 |
rs151111936 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TLE1 | GRCh38.p7 | 9:81676798 | AGGGTGCGGCCAGGT[C/T]TGACATATGGGCTAG | 7088 |
rs151120874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81609052 | CATTTGCAAAGACCT[A/G]CCCCCTCCCCTCCCC | 7088 |
rs151172830 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81613677 | GCATTAACTTGTGAG[C/T]GAGAAATGTTGACCT | 7088 |
rs151182832 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TLE1 | GRCh38.p7 | 9:81650290 | TGTAGGTGCAAAGGA[A/G]ATTCACAAGAGCTGG | 7088 |
rs151221865 | snp | A/G | 0.000845652 | 0.0205453 | missense | TLE1 | GRCh38.p7 | 9:81616127 | CTTGCTCGCGGAGAA[A/G]AAGGGTCCTCAACAA | 7088 |
rs151236625 | snp | A/G | 3.29451e-05 | 0.00405851 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593100 | GACGCAGCCCTTCCC[A/G]CCTGTGTACACGTGT | 7088 |
rs151241206 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | TLE1 | GRCh38.p7 | 9:81656182 | ACAAAAACAGAACTG[C/G]GTCAGCCCCACCCAG | 7088 |
rs151255239 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81603114 | TGCACATGCTGCTCT[C/T]TCCACCTAGAGGTTC | 7088 |
rs151259019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81667657 | AAGCCATTCCTGGCC[C/T]CTCAAACTCAGTGCT | 7088 |
rs151322847 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | TLE1 | GRCh38.p7 | 9:81641885 | AAATTAGCCAGGTGT[A/G]GTGGCGCATGCCTGC | 7088 |
rs180676614 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81626170 | TGCCATGCTGATTCC[C/T]CTTGGGAACTTTCTC | 7088 |
rs180681781 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81607351 | ATACACACACACACA[A/C]ACACATATAAGGAAT | 7088 |
rs181010278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81677856 | TTCAGGGATGATCAG[C/T]AAGCTACATATACAA | 7088 |
rs181033327 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686823 | GCCAAAGCAGGTGAG[C/G]TTTCTTCTTTATACT | 7088 |
rs181051381 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588148 | TCTTTCCAGGTCTGG[A/C/G]AAAGTGTTTAATTGT | 7088 |
rs181054572 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81659837 | AGTTTCATCAAAATC[A/G]AGTGAGCTGATGAGC | 7088 |
rs181087719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644975 | CACTGCACTCCAGCC[C/T]GGGTGATAGAGTGAG | 7088 |
rs181105439 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689739 | ACGCGCTCCTCCCCG[C/G]AGCGTATGGCAGCGC | 7088 |
rs181108089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673078 | AGGAGTTTGTGACCA[C/G]CCTGGCCAACATGGT | 7088 |
rs181127325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81657120 | CTTTTCATGTATTTA[C/T]TGCTCCACTCTATGT | 7088 |
rs181130049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81640429 | CTTGTATTTTACAAA[A/G]CAATTTGAGAAAGGA | 7088 |
rs181140962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81622329 | CAGAGGCTGGGTGTG[C/T]TGACCAGTTTTAAGT | 7088 |
rs181148070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603478 | CCATAAAATTTCCCA[C/T]GAGAAAGGTGCCCTC | 7088 |
rs181208497 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81599564 | TGGCTGGGAGGAATA[A/C/G]TGACATGGGGCTCAT | 7088 |
rs181240340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612150 | GCGAATGCATCTCCA[A/G]GAAAGAAAAGACTCC | 7088 |
rs181248284 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81677085 | CTACCAAAATGTAAC[A/C]ATTAGCTGGGTCCGT | 7088 |
rs181249755 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659637 | CTACAACAGTCTTTC[A/T]TTCTCCTTACCTATG | 7088 |
rs181259186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630189 | CCAAAGGTTCTCAGA[C/T]TTTGGTCCGAGGATC | 7088 |
rs181260187 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81644538 | AGATGGATAAGCACA[C/T]TGGTAGCAGCCAGAG | 7088 |
rs181263677 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81625661 | CAGAGAGCACCCAGT[A/G]GCGTCAAAAGAAAAT | 7088 |
rs181270893 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607096 | AGAGAGAGAGATTTT[A/C]ATTATTTTAGAGCAA | 7088 |
rs181313085 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81669309 | TCTCCATCTGTCTAA[C/T]AGACATGTGGATAAA | 7088 |
rs181332335 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633064 | TATACAGATCAAAGT[A/G]TATTTCCAAGTAAGT | 7088 |
rs181396886 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686002 | GACCAATTTGGAAAA[A/G]CCATAAACTATCTAG | 7088 |
rs181398669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81591456 | CTGAGCACATTACCT[C/T]ATTAGTCAGAAGGAT | 7088 |
rs181425211 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653135 | AAGGCAGACAAATCT[A/C/G]TTGTCATATCAGACA | 7088 |
rs181437778 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81613271 | GGAGGGTGGCCCTAC[A/G]TACATTTCATATTTG | 7088 |
rs181455829 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617420 | AAAAGCTGTTCAGCC[A/G]GGCACAGTGGCTCAC | 7088 |
rs181483306 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81621780 | TGGGAGGGTTGTCTC[C/T]AGCTCAACCATATGC | 7088 |
rs181609482 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | TLE1 | GRCh38.p7 | 9:81639577 | ATTAGTAAAAGTTGT[G/T]TTTTTTTTTTGTTTT | 7088 |
rs181734637 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81663724 | GCCTCCCGGGTTCAC[A/G]CCATTCTCACGCCTG | 7088 |
rs181735826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682904 | ACCATTCCTGTTTCA[C/T]TGCCTTTTCGGTAAC | 7088 |
rs181750469 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81649713 | CTGCATTTACTCTGC[A/G]CGCAGCTGCTGCTTG | 7088 |
rs181757831 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81630844 | TTTTATACAAAGTTT[A/G]AAGAGCTACTTAATT | 7088 |
rs181866866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81685570 | CAAGGCAGAAAAATA[A/G]CATACAAACCCCCAC | 7088 |
rs181867055 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81668687 | ACTGACCAAAAATAC[A/C]CATAATTAAAAGTAT | 7088 |
rs181868605 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81626710 | GTGACTCAGTTAGGA[A/G]GACTCATGGAAAGAT | 7088 |
rs181871821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81652604 | AGAACAGAATTTGGA[A/G]GATCACCCTTGTTCA | 7088 |
rs181876303 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607932 | ACCTCATTTCATAAT[G/T]AATCAAATTATTGTG | 7088 |
rs181881247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81632722 | AAACATGAACTCTAC[A/G]CACACAGCCCTGTCC | 7088 |
rs181889813 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690025 | GGGCTGGCTAGAGAG[C/T]GCGCGGGCGCGCGCT | 7088 |
rs181897270 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81673471 | ATGGCCTAGAAGTCC[A/G]AGAGCAGGGGTAGAG | 7088 |
rs181901157 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688884 | AGGCTCCTGGCCGGG[C/G]AGCGACGGATGACGA | 7088 |
rs181902970 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81592275 | AGGCAGGAGAACGGC[A/G]TAAACCCCGGAGGCG | 7088 |
rs181905512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81657583 | AATGAACTTGTAAAC[C/T]TTTAATAATATTAAA | 7088 |
rs181912731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656433 | TTCACATTGAAGGTT[C/T]CCAGTTTTAAAAATG | 7088 |
rs181967518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588759 | GCAGCCAGAAAAGGC[A/G]AGCAAAGTCTAGACC | 7088 |
rs181977818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630662 | AGCAACCACCCTTAA[A/C]CTTTCACTGGATTAA | 7088 |
rs181982631 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81612631 | GTCTGCAAGGAGCAC[A/G]GTTGGGCCAGCCAAA | 7088 |
rs181992414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678392 | TTAATTTTTTTTAAA[G/T]CTTTTATTGTAGAGA | 7088 |
rs182014450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645721 | CTCCAGCCTGGGCAA[C/T]AAGAGTGAAACTCTG | 7088 |
rs182043466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81600808 | GTAAAGAAGGTCCCC[A/C]ACCAGTGCAGGTGGG | 7088 |
rs182044087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616452 | AGAGAAATATCTTTT[C/T]TTAAAGGAAATAAAA | 7088 |
rs182166181 | snp | C/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81603012 | TTGTCATCTTAACAC[C/T]GGAAACAGGAGTGTG | 7088 |
rs182170822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81641392 | AGGAAGAAACTGCTT[A/G]TGGGGCCAAGAATTC | 7088 |
rs182173883 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81662880 | TGAGACAGGGTCTCA[C/T]CCTGTTGCCCAGGCT | 7088 |
rs182185342 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81673001 | AACAAGGCCGGACGC[C/G]GTGGCTCACGCCTGT | 7088 |
rs182295081 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81660250 | TCATGCCTCAATGAA[C/T]CAAAACTTAATCTCC | 7088 |
rs182338795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669824 | AATGTTAATAACCCT[A/G]ACTTTATACCAACGG | 7088 |
rs182342206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81653486 | CAAAATAGCTTATAC[A/G]TACATATGACTCATT | 7088 |
rs182344561 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633939 | CCCTGCAAACTTCCA[C/G]GGTGACCTGTGTTTC | 7088 |
rs182354475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81617681 | CACTCTGGCCTAGCC[A/G]ACATAGCAAGACTCT | 7088 |
rs182365511 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589668 | CTATAAAATGGGGCA[A/G]ATAGCAGGACAGACG | 7088 |
rs182431154 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81682607 | TGAGGTAATATCAAA[A/C]CATATGACAGACAAA | 7088 |
rs182433013 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81599246 | GCTAAGTAACTCGCC[C/T]ATAACCACGGCTAGT | 7088 |
rs182445871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81623378 | GATCCTCCAAAATTT[C/T]GAATGCTATGTTGTC | 7088 |
rs182452545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648182 | GCGGCTGAGGCAGGA[C/G]AATCACTGGAACCCT | 7088 |
rs182543606 | snp | C/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691005 | ATTGCCGCATTTATG[C/G]TTTTGTTTGAGGAAC | 7088 |
rs182561349 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81675741 | GAGTCTCGCTCTGTC[A/G]CCAGGCTGGAGTGCA | 7088 |
rs182562968 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81658684 | AGGTGAGGGTACACA[C/G]CTTACCCAACAATGC | 7088 |
rs182575760 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81643036 | AAGAGTACAACTCAC[A/C]GAAGCAGAGAGTAGA | 7088 |
rs182579127 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81623960 | ACTAGGATGTCCAGA[A/G]ACAGAGGTGATTTGC | 7088 |
rs182588286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81605364 | TGTAACAACAAAAAA[C/T]GGACTTGGATTTGGT | 7088 |
rs182647663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81601997 | ACACGATTATAATCC[A/G]AGCTCTCAAAAGTGT | 7088 |
rs182689787 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81678648 | GGCAAAACTCCGTCT[A/C]TACTAAAAACACAAA | 7088 |
rs182703413 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81660720 | CATGCCCAGCTACAT[A/G]TATGTTTTAACTGAG | 7088 |
rs182706354 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81646166 | ATGTGGGGAAATTAA[A/G]AAGTAAATGCTTCAA | 7088 |
rs182716010 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661329 | GTCTAACTGCAATAC[A/G]GAAGAGCCCACTCCT | 7088 |
rs182717887 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81627501 | CTGGGGCTTTCCTTT[A/G]AAGGGTTCACCCTAT | 7088 |
rs182723853 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81609940 | TTCTGAGGGGTCAGG[A/C/T]GAAGAGGGCCAGCCA | 7088 |
rs182731037 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81628872 | CTGAGTTAGGAAGCC[C/T]TTTCTGAGAATTTGA | 7088 |
rs182751409 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585370 | GCTCTGAAGGGCATA[C/T]TAAAACAATAGAATT | 7088 |
rs182847716 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683542 | TGATTACTAGCTGCA[A/C]CAAATGCCTCCTCAG | 7088 |
rs182872306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81650393 | AGAAAACAAACATGT[C/T]CCACAAAGTTTAACC | 7088 |
rs182906110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81613719 | GCCAGAATTAAAACT[C/T]GAGCTAGAGACACAG | 7088 |
rs182994290 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679079 | CCTGAACCCAGGAGG[C/T]GGAGGCTGCAGTGAA | 7088 |
rs182999130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684505 | AAAAATCAAAGAGTG[C/T]GGAGTTACAAAAGCA | 7088 |
rs183000278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81665558 | CTGCTTGGGCACAGA[C/T]AGCAACACTAATTGC | 7088 |
rs183003559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81646573 | CATAAGAATAAGAGG[C/T]CAACCTCATCCTCTT | 7088 |
rs183005033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671179 | TCTCAAAACAAAAAA[C/G]AAACAAGGATGAATA | 7088 |
rs183011539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651393 | CACGGTTCACCAGAT[A/T]CATTAATGCAGAGCA | 7088 |
rs183013490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631828 | GACTATCTCACCGGG[C/T]ATGGTGGCTCAGGCC | 7088 |
rs183020619 | snp | C/T | 0.00767652 | 0.0614762 | intron-variant | TLE1 | GRCh38.p7 | 9:81610348 | TTGCAGCAGGCACTT[C/T]GTGAACATCAATACT | 7088 |
rs183021322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81636260 | CTTTTAAGAGCTTGG[C/T]AATAGTGAGACATAA | 7088 |
rs183126559 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686906 | TAGCCTTCCTTAATG[A/G]ACTTTGCCTCAGAAA | 7088 |
rs183143536 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81670935 | GCACTTTGGGAGGCC[A/G]AGGCAGATGGATCAC | 7088 |
rs183143752 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81654515 | CCGGCTAATTTTTTT[C/G]TATTTTTAGTAGAGG | 7088 |
rs183170372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81664185 | CCCACCATTTTGGGC[A/G]GGATGGATCACTTGA | 7088 |
rs183182835 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631129 | TTGAACTAGAAAGTT[C/T]GTTGACTGCTAACCC | 7088 |
rs183192922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81595547 | ATTGAGGCTGGGCGC[A/G]GTGGCTCACGCCTGT | 7088 |
rs183196057 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81604916 | TCACTTCTTTACATG[C/T]CTCCCTATCACCCAC | 7088 |
rs183207189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589238 | TCTAACTCATGAAAC[A/G]CTGTTCCTCCTTGAC | 7088 |
rs183249229 | snp | A/C/T | 0.0138799 | 0.0821421 | intron-variant | TLE1 | GRCh38.p7 | 9:81665027 | ATGTGGACACCAGGT[A/C/T]CCCTGGGAGAACAGA | 7088 |
rs183264063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651225 | TGAGTGATTTGAATC[G/T]GCTCAAGGCACTCAC | 7088 |
rs183272925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631245 | CCCTCCACCCACTCC[A/T]ATGAACCCATGAATT | 7088 |
rs183278967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615189 | TATGGTGGTACCAGG[A/C]GTGGTGGTGAGTGCC | 7088 |
rs183299343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619477 | TGGCACTAACTCCAG[A/G]TGGCACTCAAAAAGA | 7088 |
rs183339071 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593434 | GAAGCATTTACTGCT[A/G]GTGCAAATTTAAAAT | 7088 |
rs183585587 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690575 | CGCGTGTCCGCAGAT[A/G]AGACGTTTTGCCCGG | 7088 |
rs183620778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81623704 | CTGCAGCACAAGAAT[C/T]ACTTGAACCTGGGAG | 7088 |
rs183645008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602280 | GCTGGGGGGATATTA[C/T]CAGCGGGGCCTTGAA | 7088 |
rs183661304 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687506 | CAGTAAGTCAGAGAA[A/G]GCAAGAACGGGTGGG | 7088 |
rs183699777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81679660 | CCCACCGACAGAAAC[A/G]GCTGTCTAAAATTTA | 7088 |
rs183759192 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81685430 | TCTTAATTCCTATCT[C/G]TCAATAAAGAGGCTA | 7088 |
rs183763894 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81668021 | TTACAAAAATTAGCC[A/G]GGCGTGGTGGCACAT | 7088 |
rs183768719 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81652220 | GCCACGTACCCCGAT[G/T]ATGGCATTCAATTCT | 7088 |
rs183772029 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81632221 | GCTATAATTTTTTGT[A/C]CCCCCAATCCCCTCT | 7088 |
rs183781774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618210 | GAATTCTTGGAAAGG[A/G]AGAGGTCCTGAATTT | 7088 |
rs183816693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675171 | AGCCTATGGAAGATA[C/T]ATGACAGATAGATAT | 7088 |
rs183820729 | snp | A/G | 0.154329 | 0.23097 | intron-variant | TLE1 | GRCh38.p7 | 9:81615727 | CAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAGAAG | 7088 |
rs183821924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677665 | ATCATAGACTAGTAA[A/C]CTACTTAGATCAGTC | 7088 |
rs183825516 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642339 | CTGAGAATTAGGGCT[A/G]CTCAATCTGTACATG | 7088 |
rs183838550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659648 | TTTCATTCTCCTTAC[C/T]TATGCCAACTCTCCT | 7088 |
rs183842267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644780 | AGGTGAATCACCTGA[C/G]GTCAGGAGTTTGAGA | 7088 |
rs183854759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81626101 | TACAGCAAAAGCAAG[A/G]CAGGTTTCCCTAATG | 7088 |
rs183860179 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81607191 | CACAACATTGGCCAC[C/T]GTGTCCACTGTCCTT | 7088 |
rs183900203 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687941 | CTCGGGGAAGGTAGA[C/G]GGGATATGGCTGCAG | 7088 |
rs183914481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661833 | TGTTGTAAGTAAGGT[A/G]GGTCATTCAGGAAGT | 7088 |
rs183919243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81655721 | AAAACTTAAAAGCAC[A/G]CAGTCCATGACCTTG | 7088 |
rs183920805 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81637315 | GTGAGCTGAGATCGT[A/G]CCACTGCACTCCAGC | 7088 |
rs183928558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620728 | ATCTACAGGTTTACA[C/T]ACTTAAAAGGGAGAC | 7088 |
rs183949303 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81604400 | GACAAATTCTAGCCA[A/G]AAGAGAAGCCTCAGG | 7088 |
rs183955569 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81635286 | TACTGAGACCTAGAA[C/T]GGGTAGGACCGTGGA | 7088 |
rs183982200 | snp | A/C/T | 0.000412922 | 0.0143633 | intron-variant | TLE1 | GRCh38.p7 | 9:81584401 | TCCTGGCTTCAGAGG[A/C/T]GACACTGTGGTCAAA | 7088 |
rs183989659 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81629839 | TTAGGGGACCACCAT[C/T]ATATATGCAATCCAC | 7088 |
rs184062352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683851 | TATAGAAACTCATTA[C/G]AAAACTATTCTCACA | 7088 |
rs184126096 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81600970 | CTGCGCCAGCTTTCC[A/C]GGGCCTCCAGCTTGC | 7088 |
rs184149535 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617843 | AGCCTGGACAACATG[A/G]TGAAACCCCGTCTCT | 7088 |
rs184163738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591559 | GCAAAGGCCAAAGAA[C/T]CTGATAAAAGCAGGC | 7088 |
rs184206451 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586981 | AAAAATAAATGCCAA[G/T]TCATGATCGAAAGAA | 7088 |
rs184317255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662062 | TTCAAATGAAAAGCA[C/T]TCCATGCATGAAGCT | 7088 |
rs184318844 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81680878 | TGAGATGTTGACTTA[G/T]GGGGAAAAAAAATCT | 7088 |
rs184332650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647450 | ATTAAAAGTCATTCA[C/T]GCACAACAACTTAAT | 7088 |
rs184341206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676042 | TTTTAATCTGAATTC[C/T]ATGGACTTGTTGAAG | 7088 |
rs184458192 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81625050 | GAATGCTCAGTATCA[C/G]AAACATAAAGAGGGT | 7088 |
rs184463704 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606822 | AGAGAGGCAGTAAGA[C/T]TGTATATAACCCAGA | 7088 |
rs184464772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662694 | CAAAAGTGAAACTCC[C/G]TATCAAAAAAAAAAA | 7088 |
rs184471828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81659097 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 7088 |
rs184479143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630433 | TCATTAATAATGTTA[C/T]TTGTATTAACACAAT | 7088 |
rs184573322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681166 | TGCTGAAATATCACA[A/T]GGAGCTCTTTCCCTT | 7088 |
rs184588991 | snp | C/G | 0.0752113 | 0.178743 | intron-variant | TLE1 | GRCh38.p7 | 9:81684806 | GATGAAAAAGTGAAT[C/G]TCAGCGTATCTCCAG | 7088 |
rs184592084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646792 | CCATCCCCTACACAA[A/G]AACATCTAGTCAGAC | 7088 |
rs184592575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647871 | AACACCATGAAATGG[A/G]CCAACAGGTGGTTAG | 7088 |
rs184597386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629288 | AGCCAAAATTTAATG[C/T]AATTTATCCTTAAAT | 7088 |
rs184602180 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81610889 | CCTACTTTGTGCAGC[A/G]TTAAGGACAGCATGT | 7088 |
rs184614318 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81651936 | GGCAAAATACCAAGA[C/T]CCCGGTCTGTTTAAA | 7088 |
rs184614678 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81612543 | GGAGTCGCAGAGAAA[C/G]CCTCCTAATTTCTAC | 7088 |
rs184631496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81615772 | CACAGATGCGTGTAC[A/G]CCCTCTAATCATGGC | 7088 |
rs184730294 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81667487 | GTAGAAAAGGAACTT[A/T]CTGCACATGGGCCAT | 7088 |
rs184746527 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688653 | GGGCAAACAAATCCA[C/G]ACGGACTGCTTTTCT | 7088 |
rs184754908 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81672271 | AAGAGTAAACAGCCT[A/C]AACTTCCAGTTTGAC | 7088 |
rs184755514 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631877 | GGAGGCTGAGGCAGG[C/T]GGATCACCTGAGGTT | 7088 |
rs184786922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589933 | CAATGACACTTCATG[C/G]ATTTCTACAGCGGAG | 7088 |
rs184861177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591272 | GTAACTGCTTCTGGT[A/G]TCCTGCATCACAGAG | 7088 |
rs184901003 | snp | A/G | 8.33576e-05 | 0.00645538 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587856 | ACCAGATTGAATAAT[A/G]ATTTCCTGCCAGAGC | 7088 |
rs184904143 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598154 | TGTCAAAAACCTTCA[A/T]TCGCTCTTCAAGCTC | 7088 |
rs184917135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616291 | TAAATGAGCAATATG[G/T]TGTCGGCAAACATAC | 7088 |
rs184993122 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81597080 | GGCTACGTCAACTGC[A/G]GTCTTGCCAATCAGC | 7088 |
rs185002328 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81595917 | GCTTCTCAAAGATCT[C/T]GGTGCCATGAGAGAA | 7088 |
rs185014473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686867 | CCCTCACCATCACCA[A/G]TGATGGGCAATGTTA | 7088 |
rs185014597 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81669860 | CTTTGCTGGTTTGGC[C/G]GAGCGACTTTTTAAA | 7088 |
rs185028611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81653544 | TCCACCCCTTCAAGG[A/G]CAGCATTAAGACAAC | 7088 |
rs185036860 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634571 | ATCCTCACATCTACA[C/G/T]TGTCACTTTCTGGTA | 7088 |
rs185042994 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618165 | ATACAATGTAGGCAT[A/G]TGGAAAAAGCAGGAC | 7088 |
rs185106861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81600860 | GACAGAAAGTTAGAG[A/G]AGGAGCAAGTGTGCC | 7088 |
rs185136382 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81673002 | ACAAGGCCGGACGCG[A/G]TGGCTCACGCCTGTA | 7088 |
rs185143640 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689817 | TCCGCCGTCTCCTCG[G/T]TCTCCCTTCCCATCC | 7088 |
rs185147420 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | TLE1 | GRCh38.p7 | 9:81639585 | AAGTTGTTTTTTTTT[G/T]TTGTTTTTTTTTTTT | 7088 |
rs185162474 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81673092 | AGCCTGGCCAACATG[A/G]TGAAATCCCGACTCT | 7088 |
rs185165629 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81657240 | AGTTTGCTCAGCTTG[C/T]CACTTGTCTTTCAAC | 7088 |
rs185175772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81640989 | AATCACAGACTTAAC[C/T]CAACCCAAACTAAAA | 7088 |
rs185183452 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81622625 | TACTACTGTAATTTC[C/T]GCTTGAGCGGCTTAA | 7088 |
rs185190476 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81603650 | CCACAATTTACTGCC[C/T]CCAGCCCAAAACTCT | 7088 |
rs185243395 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689040 | CCGCAAGTGCCCAAT[A/G]CTCCTCGAGCCCGGG | 7088 |
rs185253972 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81656447 | TTCCAGTTTTAAAAA[A/T]GATATATGCTCACTT | 7088 |
rs185292214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659200 | GGCGTGAGCCACCGC[A/G]CCTGGCCTCTCGTAG | 7088 |
rs185392774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676739 | CTGAAGACAATTTAC[A/T]TCTGCTATCTTAAAG | 7088 |
rs185416892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656193 | ACTGGGTCAGCCCCA[C/T]CCAGTTCATTTGATC | 7088 |
rs185417445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644216 | CATAGACCCAGTGAT[C/T]CTACTCCCAGAGACA | 7088 |
rs185427581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81621597 | TTTAAAATAGAAGGG[A/G]CTGGGGGATACCTTT | 7088 |
rs185463712 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583386 | AATCTTTGACCTTGA[A/G]TCACAATAGTATCAT | 7088 |
rs185549670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638058 | CTCTACTGAGACTTC[A/G]CATTTCCCCCACTGC | 7088 |
rs185562641 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81643297 | GCTGGAGTACAATGG[C/T]GCGATCTCGGCTCAC | 7088 |
rs185580946 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81605834 | CCATTAGAGTGAACA[A/G]GCAACCTACAGAATG | 7088 |
rs185619278 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81599716 | AATTTTTCCAGTTTG[C/G]CCATTTGCGTATTCT | 7088 |
rs185651196 | snp | G/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586425 | GCATGTTACTGTACT[G/T]AATACTGTAGGCAAC | 7088 |
rs185705994 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81624808 | TAAACAAAATCACCT[C/T]ATTTACATCTCCTAC | 7088 |
rs185807592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602633 | TTTTGAAGCATTTTG[C/G]ATTTTGAATTTTCGA | 7088 |
rs185857610 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621841 | CAATCCCAAGCCTCT[G/T]GGCCCGCCTCAGGGA | 7088 |
rs185868608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603013 | TGTCATCTTAACACC[A/G]GAAACAGGAGTGTGG | 7088 |
rs185885686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81678700 | CGTGCCTGTAATCCC[A/G]GATACTTGGAAGGCT | 7088 |
rs185910076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677888 | TCTATCCCTTCCAGC[A/G]TACAGTGGTGTATAT | 7088 |
rs185940772 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81607496 | AGCAGCTGAACACAC[A/G]CCCCGTACCTCTAAC | 7088 |
rs185957296 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583980 | CATGGCCCCTCTGTC[C/T]GCTTGGCCTTGGTGC | 7088 |
rs185982105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588828 | TGGGAATTTCAACAC[C/T]GAGAAGAAAGTTACC | 7088 |
rs186017622 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81664552 | CTAATCACATTTTGG[A/G]GAAATCCAAATTTAA | 7088 |
rs186040942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683049 | CTTGATTTGGATGCA[C/T]TTTCACTTTAAAACT | 7088 |
rs186041132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663751 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 7088 |
rs186041319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631130 | TGAACTAGAAAGTTC[A/G]TTGACTGCTAACCCT | 7088 |
rs186042060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659886 | ATTCCAAAGTGCTGT[A/C]CAAATATGAGAGATC | 7088 |
rs186055113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649981 | AATTCATATACTAAT[C/G]CAAAAATTACAATGA | 7088 |
rs186059977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81626409 | AAGCCATCACCCTGC[A/G]CTGCACTTTTTGCTA | 7088 |
rs186089686 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588282 | GAAATGGGGACGTTA[C/G]AAGCACAGGGTGTAC | 7088 |
rs186152553 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686245 | ATCCGGCCCTTGCAC[A/C]ATCTTCACTCTTAGG | 7088 |
rs186165911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81651090 | TGTCTGTGGCCGTCA[C/T]TGGACTATGGCACTC | 7088 |
rs186172877 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653251 | CCCAGTATTCCAACT[C/T]CTAGTCCAATAAACT | 7088 |
rs186173945 | snp | A/G | 0.00250146 | 0.035277 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685728 | TCATAATACTGTAAA[A/G]AGAAAAAAGAATCAA | 7088 |
rs186183838 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81645778 | ATAAAATAAAAATAA[A/G]TGCTTGAGGGGATAG | 7088 |
rs186187142 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81668942 | GCTCCTGTGTGTTTT[C/T]AGAAAACATCCTAGA | 7088 |
rs186189195 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81626712 | GACTCAGTTAGGAGG[A/C]CTCATGGAAAGATAG | 7088 |
rs186194351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617423 | AGCTGTTCAGCCGGG[A/C]ACAGTGGCTCACGCC | 7088 |
rs186197082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81608019 | GCAGGTGACAGGGTA[A/G]GAAATTCAATTTTAT | 7088 |
rs186299095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662941 | CAACCTCTGCTTCCT[A/G]GGCTTAAGCGATTCT | 7088 |
rs186300959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81648324 | TCACATGCCAAAAGA[A/G]AGAAAGAAAAAAAAA | 7088 |
rs186311388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630726 | TCTGCCAAGTAAAAT[G/T]AGACTTTCTAATTCA | 7088 |
rs186314916 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669411 | TATATTAATGAGGGG[A/T]AATAACCTTCTAAGC | 7088 |
rs186317922 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81612777 | TAAAACTAAAAGAAG[C/G]CTGGGCAAGGTAGCT | 7088 |
rs186335678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81633215 | AAAAGAAAAAAGCCA[C/G]GTCACTGAGAGAGAC | 7088 |
rs186445978 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690100 | CGAGTTAGCAAAAAT[C/T]CTGCCACTTGCTCAC | 7088 |
rs186539823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81592033 | TTAAGGCCAGTGGTA[C/T]GTGCTCTGTAAATCC | 7088 |
rs186569604 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593754 | CAACCTCCAAAAAAA[A/C]AGCTTTCTAAAAATA | 7088 |
rs186608027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599399 | CAGGACAAAGACACC[C/T]ACCCCACACATCGTG | 7088 |
rs186682379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688104 | TCCCCAGCCTTACAC[C/T]GCTGAGGGCGAGAAG | 7088 |
rs186684113 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81671800 | CTTATAAGATTCAAA[C/T]GTCAGCAGTTCCCCT | 7088 |
rs186727234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613273 | AGGGTGGCCCTACGT[A/G]CATTTCATATTTGTA | 7088 |
rs186833604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675759 | AGGCTGGAGTGCAGT[A/G]GCATGATCTCAGCTC | 7088 |
rs186844665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81658807 | CAATAATTCTTAGTA[C/T]TATCTCTTGCTTCAA | 7088 |
rs186851168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643067 | ATGGCGGCTGCCTTG[C/T]GGGGTAGGGGAAAAT | 7088 |
rs186862624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624473 | TCCTAGAGTCTATAC[C/T]TTGAAAGATTTTAAT | 7088 |
rs186892639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632856 | ACAAGATATGGAAAC[A/C]TAGCAACCAAGATGC | 7088 |
rs186930627 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81630935 | GGACTGAATTAAATG[C/G/T]TTAGGTTACAATTAG | 7088 |
rs186969233 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655646 | ATTTCATCATTTTGT[A/C]AATGCTTACTAAATG | 7088 |
rs186983761 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81619519 | ATCAGCTATAGGCTT[A/G]GGCCAGCCAGCAGGA | 7088 |
rs186985147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81592883 | TTTAAATGGGGAGCC[A/G]AGGGGGTTAAATAAC | 7088 |
rs186986025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81660745 | ACTGAGCAGAAATAC[A/G]GCCAAGGACCTCAGA | 7088 |
rs186988558 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81657671 | AGTGGTCTCTCGGTA[A/T]CTGTGAGGGATTGGT | 7088 |
rs186992164 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81682608 | GAGGTAATATCAAAC[C/G]ATATGACAGACAAAA | 7088 |
rs186992791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646348 | TTGCTCTTTCCCTTC[A/G]GAAATTTAATAAAAG | 7088 |
rs187006965 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81623545 | GCACTTAGGGAGGCC[A/G]AGGCAGGCAGATCGC | 7088 |
rs187038815 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81678511 | CCTGGCTTGCAACTT[A/G]GTAATTATTAAAAAT | 7088 |
rs187073003 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81652633 | CACAAAAGGGGTTCA[C/T]AAGTTTACAGCAATT | 7088 |
rs187095223 | snp | A/G | 0.000807402 | 0.0200761 | intron-variant | TLE1 | GRCh38.p7 | 9:81616721 | AAAAGAAACATTAAC[A/G]CCATTTACTAAAAGC | 7088 |
rs187193721 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81674342 | TGACCAGCTGTTTGC[C/T]CAAGGCATCAAGAGG | 7088 |
rs187206890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81641522 | AGGAATGGGAGAAAA[C/T]ATTTGCAAACCATAC | 7088 |
rs187220912 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81604446 | CCAAACACTGAAGAG[C/T]TGCCATGAGGATGAT | 7088 |
rs187292879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665773 | AATGACAAAGCAACT[C/G]TATTCATTGGTTCTC | 7088 |
rs187303459 | snp | A/C/T | 0.00137277 | 0.0261632 | intron-variant | TLE1 | GRCh38.p7 | 9:81590772 | CAGCTGCTAAAGAAG[A/C/T]GAACCCCTCCTTAGA | 7088 |
rs187339833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81602037 | CATAAGATGTTTCAC[A/G]GTGCAACTGGAGGGA | 7088 |
rs187340430 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TLE1 | GRCh38.p7 | 9:81636508 | GCGGGTAATTAAGCA[C/T]GGCACTAATTAAAAG | 7088 |
rs187403451 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81680426 | GATCCTGCCCTAATA[A/C]AAAATTTGGACATGT | 7088 |
rs187404544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661836 | TGTAAGTAAGGTAGG[A/T]CATTCAGGAAGTTAA | 7088 |
rs187412118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687045 | TGAAAAATAAATACA[C/T]GAAGTGCAAATATTG | 7088 |
rs187419581 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81647034 | ACCCGAATTTCATGG[G/T]TTTTTTTTTCTCTTG | 7088 |
rs187427880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629484 | CAAACCTCTATAAAG[C/T]TGCTAGCTTTATTGT | 7088 |
rs187435325 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611325 | AAAGTGTAACATAGG[C/T]ATAGAAAGAGAAAGC | 7088 |
rs187470408 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81642595 | GCTACTCCAGAGGCT[A/G]AGGCAGGAGAACTGC | 7088 |
rs187478052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81623894 | AAGAGGCCAAAGCAA[C/T]CACTGAGACATTTCG | 7088 |
rs187486538 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81605062 | ATGCCTGGCATCGCA[A/C]ACAAAGCCTGACAGT | 7088 |
rs187525094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81679196 | TGTAATTTTGCTAAA[C/T]CACAGGTTATTTGAT | 7088 |
rs187540048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646581 | TAAGAGGCCAACCTC[A/G]TCCTCTTAAACTTCA | 7088 |
rs187542633 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81631426 | GGCACATACCACGTG[G/T]TATCACTTCCACAAT | 7088 |
rs187550393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81615232 | TACTGGGGAGGCTGA[A/G]GCAGGAGAATTGTTT | 7088 |
rs187554249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81610473 | ATAAGCACCCCTGAA[C/T]GCCACAAGACCCACT | 7088 |
rs187662561 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81605373 | AAAAAATGGACTTGG[A/G]TTTGGTATCTTTTCC | 7088 |
rs187790032 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661539 | GATGGATCATAAAAA[A/T]ATGGTGCTTATGCTG | 7088 |
rs187800242 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627734 | TTAATTCATAAATAT[C/T]TAGGCAAAAACAGTA | 7088 |
rs187910796 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589809 | AAAAGGTGGAGAGGG[C/T]GTTCGGCCCTGGCTC | 7088 |
rs187931026 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81595691 | GGGTATGGTGGCGGG[C/T]GCTTGTAGTCCCAGC | 7088 |
rs187939792 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684243 | AGATCTTCTAGCCCA[C/T]TTACTATCAAGAAGT | 7088 |
rs187948332 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81665045 | CTGGGAGAACAGACT[A/C]AAATAACTTGCCTAA | 7088 |
rs187948525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81651270 | AGAAAGGACGGTCCC[C/T]TGTTTCAGCTCCTTC | 7088 |
rs188090697 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610077 | CTGCCTATTTATAGA[A/T]AGTGTTAACACTCCT | 7088 |
rs188142444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589423 | CAATAGGCTTTACAT[A/G]GCCCTATTACATGCA | 7088 |
rs188150146 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687610 | GAAAGCGGACCCTCC[C/T]CGGGCCCCGGCTTCT | 7088 |
rs188156162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677715 | CAGTCTCATGGTACA[C/T]GTATTTCAGTAGTTT | 7088 |
rs188158434 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81655088 | AAGGCAGGAAAGGCC[A/G]GGTGCGGTGGCTCGC | 7088 |
rs188173138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659819 | ACCACCAATCTACTT[A/G]AGAGTTTCATCAAAA | 7088 |
rs188175281 | snp | A/G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644887 | TAATCCCAATTACTC[A/G/T]GGAGGCTGAGGCAGG | 7088 |
rs188203321 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81637618 | ACTGGGTTCTTCCAT[C/T]CATTGCTTGGCTACA | 7088 |
rs188212541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620811 | TGGAAATGTGCTTCT[C/G]TCCTATTTACTGTTT | 7088 |
rs188223947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81597150 | AGATAGGAATAATAA[C/T]AAAACACAGAGGTCG | 7088 |
rs188285980 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81601075 | TCCATATCTATAGTT[C/T]ATTGGTTCTGTTTCT | 7088 |
rs188292051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651827 | TTTTCCCACTTAAAA[C/G]TAGATTTAGGGACGG | 7088 |
rs188297541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675183 | ATATATGACAGATAG[A/G]TATTACAAAATGTTA | 7088 |
rs188311960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81615746 | AAGAAGAAGAAGAAG[A/G]AGGCAATGAACACAG | 7088 |
rs188339598 | snp | C/T | 0.000346915 | 0.0131658 | missense | TLE1 | GRCh38.p7 | 9:81616116 | AGTGGGCAGGGCTTG[C/T]TCGCGGAGAAGAAGG | 7088 |
rs188367658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591668 | ATATGGCTAAAGTTT[C/G]CTTACATGCTTTTAA | 7088 |
rs188369234 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583457 | AAAGAAAACTGTCAT[G/T]AGTAAACCTTCAATT | 7088 |
rs188379036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81603265 | CCTCTGTAATAGCTC[C/T]GTGGTAGCCTCAGGG | 7088 |
rs188425802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81671145 | TGCACTGCAGCCTGG[A/G]CAACAGAGTGAGACT | 7088 |
rs188445535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81671285 | TTGGAAGGCTGAAGC[A/G]GGCGGATTGCTTGAG | 7088 |
rs188448598 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81635879 | AATGTTTAGGGTCAG[A/G]CACAGTGGCTCACTA | 7088 |
rs188581975 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690888 | GGAACTTGAGTTAAA[A/G]GGGATTTTGAGATTG | 7088 |
rs188588873 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631829 | ACTATCTCACCGGGC[A/G]TGGTGGCTCAGGCCT | 7088 |
rs188594566 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81657959 | CTGTCACCTAGGCTG[C/G]AGTGCAGTGGCACAG | 7088 |
rs188692214 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81656854 | CGCCTCCACACAGAT[C/G]TCTAAAAGGAATCCC | 7088 |
rs188698274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81640041 | GTGTGGAGGTCACTG[C/T]GGGGGAGGGAAAAGA | 7088 |
rs188702065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81680999 | TCACATCTAAGGAAA[C/T]ATCCCACAGGTGAGT | 7088 |
rs188702286 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81662074 | GCATTCCATGCATGA[A/G]GCTGTTCACTGCAGC | 7088 |
rs188707460 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81621883 | GGAGCTGGGCTCTTT[C/T]ATTCATGACTGTTCA | 7088 |
rs188714716 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81596257 | GATTCACAATGCAGC[A/G]AGCTGCTGTCAGAAG | 7088 |
rs188727842 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654857 | GGATTTTATTGTTCA[A/T]AGCTTCCCTAAGTCT | 7088 |
rs188740296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618628 | ACTAACGAAAATCTG[C/T]TTTCTCTTGGTAAAG | 7088 |
rs188852563 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81625282 | GCTTCCTAAGGGTTA[C/T]ATCTAACTTGCACTA | 7088 |
rs188861023 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606884 | TTCTGATATTAAGTC[G/T]ATCTTCCTCACATAA | 7088 |
rs188928497 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685961 | TAACATCTGCCTCAC[A/T]TATTTGCACTTCAAG | 7088 |
rs188945251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659128 | TGGCCAGGATGGTCT[C/T]GATCTCCTGATCCTC | 7088 |
rs188963312 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81624967 | ATACACTTGTGGGTA[A/C]AGGGTCAAGTACCCT | 7088 |
rs189009632 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587221 | TTTTTGAGCTCTCTG[A/G]TGCGGGGTAAATAAA | 7088 |
rs189038550 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81681981 | CCGGGTGTGGTAGCT[C/T]ATGCCTGTAATCCTA | 7088 |
rs189065112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648076 | TGGGAGTTCAAGACC[A/G]GCCTGGCCAACATGG | 7088 |
rs189077986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663193 | AAGGGAGATAAGCGC[C/T]GTCAGGCTCACCACG | 7088 |
rs189078051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648667 | TTTAGTTCCAAACTC[C/T]CCAAATAATAAAGTG | 7088 |
rs189088811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81630772 | TAGATAAGTACTATA[A/G]TATTTTAGGCACTAA | 7088 |
rs189199278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81667785 | GGTTGCTGCCTTCCC[A/G]GATGGAACCTGGAAT | 7088 |
rs189210719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81607271 | AATGCAAGGTGCTCA[C/T]AAGCCAAGGACATGA | 7088 |
rs189215282 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81631936 | GGAGAAACCCCGTCT[A/G]TACTAAAAATACAAA | 7088 |
rs189224882 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TLE1 | GRCh38.p7 | 9:81676052 | AATTCCATGGACTTG[C/T]TGAAGGATCTTGAGA | 7088 |
rs189242311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81643526 | CAGGCATGAGCCACC[A/G]CACCCAGCCCTTTGT | 7088 |
rs189256759 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81606278 | ATTACTGGGTGTATA[A/C]CCAAAGGATTATAAA | 7088 |
rs189284967 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598276 | TCCCCTAAAATATCA[C/T]ATGCTGTCACATCTC | 7088 |
rs189335200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662731 | AAAGTGGCCAAGCAC[C/T]GTAAATTGATATCCA | 7088 |
rs189354608 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630516 | CAGTAAGTATCAAAA[A/C]TCAAAATATTAACCT | 7088 |
rs189408935 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588042 | TTCCCTGTTTTCCAC[A/G]ATCCAAGTGCTAAAG | 7088 |
rs189466499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682773 | GTCTACCTCTACTGT[A/G]TAGAGATATCTAGAG | 7088 |
rs189470103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684913 | TCATTTAGCTTTTCT[C/T]CTCTTATGAGGTCCT | 7088 |
rs189485269 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81626144 | ACATTATTCAAATGG[A/G]TTTCTTTAGCTGCCA | 7088 |
rs189490974 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81651937 | GCAAAATACCAAGAC[A/C]CCGGTCTGTTTAAAA | 7088 |
rs189524129 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81602454 | ACACAAAATTCATTT[C/T]TGTTTCATACAGACC | 7088 |
rs189561000 | snp | C/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689990 | AGCGGCGGGGCTGGG[C/T]TGTCAATCAAAGTAA | 7088 |
rs189574147 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81631220 | CTTGAAGGGGACAAC[C/T]AATAACCCTCCCTCC | 7088 |
rs189579995 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | TLE1 | GRCh38.p7 | 9:81673260 | CCTGGGGGACAAGAG[A/C]GAGACTTCATTTAAA | 7088 |
rs189580342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657532 | CAAAGTAGACTTGAA[C/G]ATGGTCGGAGGACAG | 7088 |
rs189587159 | snp | A/C/G | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81614499 | TTTCATGTGCTTTAC[A/C/G]ACACAGTCCAAGAAC | 7088 |
rs189591157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81641196 | CAATTCCTATCTTGG[A/G]AGACAGCAAAATAAA | 7088 |
rs189607710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668115 | GGTCGCGATGAGCCG[A/G]GATCGCGCCACTGCA | 7088 |
rs189609882 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81685560 | GACAGGAAACCAAGG[A/C]AGAAAAATAGCATAC | 7088 |
rs189619278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652498 | TTCTAAACAACACCA[C/G]TCACTACTTCTGGCT | 7088 |
rs189623358 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632437 | TTCCCCCCAAAACTT[A/T]TACCAAAAAAGTTAT | 7088 |
rs189626727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616435 | AGGCATTCAAAATGT[C/T]TAGAGAAATATCTTT | 7088 |
rs189691829 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600382 | AACTGACATCAAAAG[G/T]AAGGTCCTCCCAGCT | 7088 |
rs189720856 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81633897 | CAATCTAACGAGATC[A/G]AGAAATCTACAGATG | 7088 |
rs189726063 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689701 | CAGCCAATCGCGTGC[A/G]CTGCAACCAACGTGG | 7088 |
rs189726903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617559 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGCGCAT | 7088 |
rs189772922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81629845 | GACCACCATCATATA[C/T]GCAATCCACTGTTGA | 7088 |
rs189836142 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81594643 | TTCAAACCATAAACA[A/G]TAAGTGAAGTATGCA | 7088 |
rs189871368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653056 | ATAAATTTACTTTGG[A/G]AGGCATGAGAATGTA | 7088 |
rs189875361 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676773 | CTCCCTTTCCAGGGC[C/T]GGAGTTCCCAGGGTG | 7088 |
rs189884302 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617419 | GAAAAGCTGTTCAGC[C/T]GGGCACAGTGGCTCA | 7088 |
rs189935013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603004 | AACCCATCTTGTCAT[C/T]TTAACACCGGAAACA | 7088 |
rs189975654 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81673027 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 7088 |
rs190001228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81672397 | GGAGTGTGATGGTGC[A/G]ATCTTGGCTCACTGC | 7088 |
rs190016533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647689 | GGGTGGGAAGGTAGA[C/G]GGTATTACCATCTAC | 7088 |
rs190017790 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639181 | TCCTCCTGCCTCAGC[C/T]TCCCAAAGTGCTGGG | 7088 |
rs190117164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669001 | GGACATGTCAATTCT[C/T]GTTTCCCACAGCACC | 7088 |
rs190129779 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81632980 | GATATAAAAATGAAT[A/G]TTCTTTTAAACTACA | 7088 |
rs190213051 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81678986 | TCTCTACCAAAAAAT[A/G]ATTTAAAAAAAATTA | 7088 |
rs190215262 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81660819 | ATTCAAGATATGGCC[A/G]GGCGTGGTGGCTCAC | 7088 |
rs190242791 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688856 | AAGGGGAGCGAGGTT[A/G]AAGACGCAGCGGAGG | 7088 |
rs190268339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656373 | TCCCAACTCCCTACC[C/T]ACCACACATTCCTGC | 7088 |
rs190282619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621735 | GGTGGCCAGCCCTCA[A/G]AGCTCCCCTGAAAAC | 7088 |
rs190332818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599459 | TGTGACTGTGGGGGC[C/T]GGGGGAACCGGGCTC | 7088 |
rs190340553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675592 | CTCTCAGTGGTTACT[A/G]ACTACAGATCACTCT | 7088 |
rs190346484 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81658150 | CTCCTGACCTCAAGT[A/G]ATCCACCTGCCTCAG | 7088 |
rs190357011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81642688 | GACAGAGTGAGACTC[C/T]GTCTCAAAAAATGAA | 7088 |
rs190362956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683120 | CTCTAGAACTCACTC[C/T]GACAAACCCGTTGAA | 7088 |
rs190369560 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81623926 | TCCTCTTCCTCCTCC[C/T]GCTCCTTTAATCTGG | 7088 |
rs190491169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81660628 | TCACTGTGTTAGCCA[A/G]GATGGTCTCCAACTC | 7088 |
rs190499292 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645857 | AAAACATCTCCTGTA[C/T]CTCATAAATATATAC | 7088 |
rs190509429 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TLE1 | GRCh38.p7 | 9:81627269 | TTTCTAATTACAGAG[A/C]ACAAACTCAAGTCAA | 7088 |
rs190519781 | snp | C/G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609558 | GTGACCCAGGAAGAA[C/G/T]AGCCAATTGAGTTTT | 7088 |
rs190577457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586481 | CATCCAGATACATCT[A/G]AACATTGAAAAGGTA | 7088 |
rs190600610 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81592084 | CGGAACATGGCCGGG[A/C/T]GCGGTGGCTCACGCC | 7088 |
rs190611228 | snp | A/C/T | 0.00438571 | 0.0466605 | intron-variant | TLE1 | GRCh38.p7 | 9:81683741 | TCTCTCAGCTTTTCA[A/C/T]GTTTTTCAAATTGCT | 7088 |
rs190614589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81585245 | TAGAAACTCATTGTC[A/G]TCTCCCAACCCCTCC | 7088 |
rs190637620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651175 | TAAAGACCAGCAGGG[C/T]ATCATCTCACAAGCA | 7088 |
rs190664583 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613184 | TAAACAGTTGGAGAC[A/T]GAACAGAGTGCAGCT | 7088 |
rs190667950 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81622746 | CTGAAAATGGGCCCC[A/G]TTCAACAGCAGACTT | 7088 |
rs190748173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588993 | GTGAACCATCACTTT[C/T]AAAATCTTCTCTCTG | 7088 |
rs190866046 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588733 | ATGCTGAGAGGAAGG[C/T]GGTGGGGGAGGCAGC | 7088 |
rs190876531 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81664830 | TAATACACAGATGAC[C/T]AGGCCCACCTGCGGA | 7088 |
rs190878847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81584372 | AGGCCCTGCTCCCTC[A/G]GAGGCACCTTCACTC | 7088 |
rs190927105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603710 | ATTTCTTTGTATAAA[A/T]GTGATACAAGGTCAG | 7088 |
rs190994986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686875 | ATCACCAATGATGGG[C/T]AATGTTATAAGCATC | 7088 |
rs190997494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81670763 | TTTTTTGGGTATTTG[A/C]TCTTGGATAAAATAA | 7088 |
rs191001529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81653571 | CAACTGCCTTGATAC[A/G]TAAGTACAAAAGAAC | 7088 |
rs191012068 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81634684 | ATGCGCCTCCAGGGA[A/T]GAGATCCAGCATGTC | 7088 |
rs191020321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618182 | GGAAAAAGCAGGACA[G/T]CTCAATGGTTTTGAA | 7088 |
rs191020788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589440 | CCCTATTACATGCAG[C/G]AGCCACTAGCCACCT | 7088 |
rs191168115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646431 | AGAGCTAGAAGATCC[A/G]TGTTTGTTGTAGCTA | 7088 |
rs191180737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610330 | CATTGCAGACTCAGT[C/T]TATTGCAGCAGGCAC | 7088 |
rs191191373 | snp | C/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587946 | TGTGTGTGTGTGTGT[C/G]ATCCCGCCAGTGTCT | 7088 |
rs191236080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652098 | TATCAAATAGGTCAA[A/C]GTTAAGATACACACA | 7088 |
rs191240624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81675826 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATGAC | 7088 |
rs191254916 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658828 | CTTGCTTCAACAAAA[G/T]GGTATTCTGGTAAGA | 7088 |
rs191256488 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81616219 | ATTCTCTAAATTTAA[A/G]GACAGAGCTGAAAGT | 7088 |
rs191278180 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690983 | TACACAGCAGAAAAC[C/T]GTCAGTATTGCCGCA | 7088 |
rs191307228 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664108 | CTAGTTCCTGAAGAT[A/G]ACGTCTTATTTTTAT | 7088 |
rs191323761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631014 | ATTAGGCAGGAAACA[A/C]AGCATATATACTTGT | 7088 |
rs191395588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687078 | GATTCTCATGCAACT[C/T]CTAAAGACATGAAAA | 7088 |
rs191408798 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686750 | GAAGAAACTAAGGCT[A/G]AGATGGATATAAATG | 7088 |
rs191415017 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628063 | GACTGTACAAAAATT[A/G]AAAGAAAATTGTTTT | 7088 |
rs191415313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653460 | TAAACCTCTATGACT[C/T]TGTAACTAAACAAAA | 7088 |
rs191548675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81650143 | ACAACATTTTTCCTG[G/T]ACTAAAGCCATTCGT | 7088 |
rs191590610 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81604461 | CTGCCATGAGGATGA[C/T]AGATTAGCAGTGTGC | 7088 |
rs191611316 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81681072 | AGAACAACGCATTTT[G/T]CTAAGAGAAATTTTA | 7088 |
rs191657356 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81671154 | GCCTGGGCAACAGAG[A/T]GAGACTCTGTCTCAA | 7088 |
rs191659454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81585301 | TATTAGGCAATCACA[C/T]TGCCTGCTGACTTTT | 7088 |
rs191747487 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81655382 | TAAAAAAAATAAAGA[A/C]GGCTGGAAAAACCTT | 7088 |
rs191753976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81636871 | AGCCAGGTGTGGTGG[C/T]GGATGCCTGTAATCC | 7088 |
rs191760509 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81619670 | GAATGCATCCATCCT[C/G]AAACAGACACTCAGG | 7088 |
rs191794831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602058 | ACTGGAGGGAGACCA[C/T]AGATGGGAAGGCATC | 7088 |
rs191838250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81600958 | CTTGGAGTAGAACTG[A/C]GCCAGCTTTCCCGGG | 7088 |
rs191866606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81623573 | CGCCTGTGAAAAGGA[A/G]TTCGAGACCAGCCTG | 7088 |
rs191877987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680503 | TTGATCATGATAACT[A/G]TGTTTTGTGATTTTC | 7088 |
rs191888592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81605346 | CTTAGGGCTGTTGAC[C/T]CTTGTAACAACAAAA | 7088 |
rs191896895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661852 | CATTCAGGAAGTTAA[G/T]GCAATTTTTAAAAAA | 7088 |
rs191900879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647271 | GAATGATTCCTATAA[A/C]CTCTTGTGCCAACAA | 7088 |
rs191913367 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81629540 | TTAAAGCAGTTTCCA[A/T]AAAAACTTTCACTCT | 7088 |
rs191920130 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81611440 | TCGAATCATTTCATC[A/G]CCTTCAAATAAAAAA | 7088 |
rs191948605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81674764 | AATCACCTAAAAACC[A/G]TGTAATGGTGGATCA | 7088 |
rs191962286 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81641958 | ACCTGGGAGGCAGAG[A/G]TTGCAGTAAGCGGAG | 7088 |
rs192072215 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81660209 | TAAAACTGATGCCAG[A/G]GTACATATTTAATAT | 7088 |
rs192088884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81626429 | ACTTTTTGCTACGGT[C/T]CAACTGGTCATTCAC | 7088 |
rs192175821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81624694 | CAGGATTTTTTTAAA[A/G]ACTTTAAATGTTGGG | 7088 |
rs192249418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81591187 | AGCAAGAGTTCTCTA[A/G]TCAAGATTGGGGTCC | 7088 |
rs192264346 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690351 | GGAGTGGACTGTGCA[C/G]TTAGTTGGAAATGCG | 7088 |
rs192272404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657724 | AAATCTAAGGATGCT[C/G]AAGTCCTTTATATAA | 7088 |
rs192367135 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589914 | GCAGGGACCGGGCCC[A/G]GCTCAATGACACTTC | 7088 |
rs192420822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678024 | GTGACTTGTATCCTA[C/T]TCTTTTTCTGCTAAC | 7088 |
rs192443674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645256 | CCCAGCTACTTGGGA[G/T]GGGAGGCTGAGGCAG | 7088 |
rs192451192 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81665521 | TAAAAGAAAGGAAGG[A/G]AAAAAAAAACCGTGC | 7088 |
rs192452787 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81684443 | ACAAATCTGAGAACA[C/G]ATCTAATGTACACGA | 7088 |
rs192459874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586307 | CAGGCGTGAGCCTCC[A/G]TGCCTGGCCTTGTTA | 7088 |
rs192466266 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606640 | AGCAGGTGGGGGACT[A/G]GGGGAGGGATAGCAT | 7088 |
rs192467664 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81651347 | TCCTGCAGTGGGGGG[C/T]GGAGGATGAACTCAT | 7088 |
rs192468133 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81607815 | TGGAAGAGAACTACC[A/G]GCTAAGTGAACATTA | 7088 |
rs192475575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631438 | GTGGTATCACTTCCA[C/T]AATTCTGATACCAGT | 7088 |
rs192481598 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81615582 | GCTGGGCATGGTCGC[A/G]CGCGCCTGTAATCCC | 7088 |
rs192514741 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586612 | AATGATATGCTGCTA[C/G]AGTTTATTTTAAAAT | 7088 |
rs192518319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81667953 | TGGATTGCCTGAGGC[C/T]AAGAGTTCGAGATCA | 7088 |
rs192522551 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81684961 | TCAATACTCTTTTTA[A/T]ACACCATTATAGTAG | 7088 |
rs192557784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643288 | GTTGCCCAGGCTGGA[A/G]TACAATGGTGCGATC | 7088 |
rs192561519 | snp | A/G | 0.0146672 | 0.084371 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688348 | AGCCAAGCAGAAGCG[A/G]GGAGCGCGCTGGCCA | 7088 |
rs192576281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672125 | TCTCAGCACACCCAG[A/G]TCAGAAGGCGGCCAA | 7088 |
rs192578452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655878 | AAAAAAAGAAAAGAA[A/C]AGAACAAAACCCCAG | 7088 |
rs192578970 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81605800 | AAAGAGTTTCTGCAC[G/T]GCAAAAAAAAAAAAA | 7088 |
rs192584668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81637625 | TCTTCCATCCATTGC[C/T]TGGCTACAATGAAAG | 7088 |
rs192606663 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81596373 | CTGCTGTGCTGGAGA[A/G]CCAAATCAAATGAAC | 7088 |
rs192624837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610654 | GCCAAACAGTTCTTT[C/T]CTTTGTTAGGGGCCG | 7088 |
rs192659480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647741 | GTTAACTGACTATAT[A/G]AGGTCATAAAGCTAA | 7088 |
rs192662511 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81671577 | TTGAACCCGGGAGGC[A/G]AAGCTTGCAGTGAGC | 7088 |
rs192747643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81666752 | TGCACTCCAGCCTGG[A/G]TGACAGAGCAAGACT | 7088 |
rs192753729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81631857 | CCTGCAATCCCAGCA[C/T]GTTGGGAGGCTGAGG | 7088 |
rs192824920 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81655046 | TAAAAGGTGTCCTTA[A/G]TGTCTATAGCACGGG | 7088 |
rs192831302 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | TLE1 | GRCh38.p7 | 9:81619418 | AATCACTGGGATGTT[A/T]TAAGAGTTAAATGAA | 7088 |
rs192881309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662213 | TAAATCAGTTGTCTA[A/C]AACTAAGAGAACAGT | 7088 |
rs192887167 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687936 | CCCCACTCGGGGAAG[A/G]TAGAGGGGATATGGC | 7088 |
rs192945917 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TLE1 | GRCh38.p7 | 9:81684805 | TGATGAAAAAGTGAA[C/T]GTCAGCGTATCTCCA | 7088 |
rs192958976 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651912 | TCACTTGAGTTCCAG[C/G]CCAGAGTAGGCAAAA | 7088 |
rs192966967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81615768 | TGAACACAGATGCGT[A/G]TACACCCTCTAATCA | 7088 |
rs193035261 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81636245 | TTCTTGCTCTGTCAC[C/T]TTTTAAGAGCTTGGC | 7088 |
rs193049721 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81602466 | TTTCTGTTTCATACA[A/G]ACCTTATGCACTTAG | 7088 |
rs193073866 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81676252 | CAATGCCTACTCTGG[A/G]TAACTCATCGGGAAG | 7088 |
rs193124463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661600 | TGAACCAAGCGGGAA[A/G]CCAAGATAAAAACAC | 7088 |
rs193188345 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81601749 | CCAGCCTTGAGGGTA[C/T]GAAAACAAGCTCAGG | 7088 |
rs193240930 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81659162 | ATCCGCCCACCTCAG[C/G]CTCCCAAAGTGGTGG | 7088 |
rs193244934 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81625049 | AGAATGCTCAGTATC[A/T]GAAACATAAAGAGGG | 7088 |
rs193254479 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595835 | AAAAAAAAAAAAAAT[A/T]AAAAAATAAAAGTAA | 7088 |
rs193274118 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81679364 | ACACAAGCAGCAAAT[A/C]TGAAATCATTCCTTT | 7088 |
rs193277285 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81621581 | CCTTTCTCTGCCACA[A/G]TTTAAAATAGAAGGG | 7088 |
rs193279582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646732 | TCAATCTCTTAGGGA[C/T]AGACAGGCTCCTTCT | 7088 |
rs199512359 | in-del | -/CTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632748 | TGTCCACTGAATTTC[-/CTT]CTTTTTAAGAGCTTA | 7088 |
rs199536347 | snp | A/G | 0.00199802 | 0.0315439 | missense | TLE1 | GRCh38.p7 | 9:81591015 | AGAGTGCAGCCATCG[A/G]GTAGCAATTTACAGG | 7088 |
rs199561928 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81635337 | GGGACTCCAGCCAGC[A/G]AGCCAAGCCCCCGTT | 7088 |
rs199640322 | snp | A/G | 0.0102655 | 0.0709039 | intron-variant | TLE1 | GRCh38.p7 | 9:81611756 | AACCACAGCCCACCC[A/G]ACAGCGGCCTACCAT | 7088 |
rs199666246 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618988 | CCAACCAGACAAACC[C/T]AGTACATGCAGGTTA | 7088 |
rs199672832 | snp | A/G | 8.52261e-05 | 0.00652731 | intron-variant | TLE1 | GRCh38.p7 | 9:81685651 | CTGATGTCTCATTTC[A/G]GCTTGAAGTTCAACT | 7088 |
rs199694206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81585482 | CCATCAACGGCCTCC[A/T]GTTTCCTTTCGGCTG | 7088 |
rs199700986 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666775 | GCAAGACTCGTCTCA[A/C]AAAATAAATAAATAA | 7088 |
rs199731120 | in-del | -/A | 0.0603597 | 0.1629 | intron-variant | TLE1 | GRCh38.p7 | 9:81680942 | TTAAAAAAAAAAAAC[-/A]AAAAAAAACACTAAG | 7088 |
rs199776589 | snp | C/T | 0.00199801 | 0.0315438 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634100 | CCGGCCTCTCACCTC[C/T]GTGGTGCTCTGCATC | 7088 |
rs199783944 | in-del | -/TTC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613904 | AAGACCCCTTTTCTT[-/TTC]TTTTTTTTTTTTTTT | 7088 |
rs199834935 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601602 | GTGCTACAGTGCCAG[-/A]AAAAAAAAAAAAAAG | 7088 |
rs199862703 | snp | A/G | 0.000201749 | 0.0100416 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687462 | AGCGAGGGGGACCGA[A/G]GGACGGGAATGCGGG | 7088 |
rs199895310 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637663 | TTTTTTTTTTTTTTT[A/T]AGCAAAATCCTATCA | 7088 |
rs199918261 | in-del | -/G | 0.100588 | 0.200439 | intron-variant | TLE1 | GRCh38.p7 | 9:81639772 | ATTTTTAGTAGAGAT[-/G]GGGGTTTTGCCATGT | 7088 |
rs199920121 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679312 | TTCTTCACTTTTTTT[C/T]CTTTTTTTTTCCCCT | 7088 |
rs199930827 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652888 | GACCCACCAGTCATT[G/T]TCGGAAACTCCTGGA | 7088 |
rs199937572 | in-del | -/A/TA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606776 | ACTTAAAGTATAATT[-/A/TA]AAAAAAAAAACCATA | 7088 |
rs200024311 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661220 | TTTATATATATATAT[A/C]TCTTTTTTTCAAGAT | 7088 |
rs200044325 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603970 | TTGGGCCACTACACT[A/C]CAGCCTGGATGACAG | 7088 |
rs200049907 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629302 | GCAATTTATCCTTAA[A/T]TTAATTAAAATATCT | 7088 |
rs200061519 | in-del | -/TTAAC | 0.0185938 | 0.0946107 | intron-variant | TLE1 | GRCh38.p7 | 9:81670667 | GTTACTTATTCCTTA[-/TTAAC]TTTGAGCAATTTCAG | 7088 |
rs200067136 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655863 | GTCTCAAAAAAAAAA[A/G]AAAAAAGAAAAGAAA | 7088 |
rs200073367 | snp | C/T | 6.67412e-05 | 0.00577634 | intron-variant | TLE1 | GRCh38.p7 | 9:81620602 | TCTTCCCAAGCCTCT[C/T]TGTACACATGAAACC | 7088 |
rs200131732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615950 | TGAAAAATACACTGC[C/G]AAACAGGCAAGTGTC | 7088 |
rs200133937 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | TLE1 | GRCh38.p7 | 9:81633430 | GGCAAGAACAGAAAT[-/A]AAAAAAAAGGGGGGA | 7088 |
rs200174021 | snp | C/T | 0.00299551 | 0.0385848 | intron-variant | TLE1 | GRCh38.p7 | 9:81660235 | AATATACTTTCAAAG[C/T]CATGCCTCAATGAAC | 7088 |
rs200178334 | in-del | -/AAATAAAAAT | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81661125 | GAGACTCGGTCTCAA[-/AAATAAAAAT]AAATAAAAATAAATA | 7088 |
rs200182684 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666776 | CAAGACTCGTCTCAC[A/T]AAATAAATAAATAAA | 7088 |
rs200255398 | snp | G/T | 0.423726 | 0.179776 | intron-variant | TLE1 | GRCh38.p7 | 9:81643246 | TTTTTGTTTTTTGGT[G/T]TTTTTTTTTGACAGA | 7088 |
rs200276118 | in-del | -/AAC | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686224 | TTTCTCTGTACTCCA[-/AAC]CCAAAATCCGGCCCT | 7088 |
rs200276956 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584308 | AGGACTCTTTGGACT[A/G]GAAGAGAAAACAATG | 7088 |
rs200351770 | in-del | -/G | | | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689655 | TGAGCCCGGGAGGTT[-/G]GGGGGTGGGGGGGGG | 7088 |
rs200355393 | snp | C/T | 1.67866e-05 | 0.00289707 | intron-variant | TLE1 | GRCh38.p7 | 9:81584574 | GGTTAAAATTCCTAC[C/T]ATACAATTAGCAACT | 7088 |
rs200377772 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587578 | GCCCTGATCTGTTTG[A/G]CCAGCCACTACCATC | 7088 |
rs200387224 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81668663 | AGAATCTATTCAGAG[-/T]TTACAGGGACTGACC | 7088 |
rs200467654 | snp | A/C | 1.66568e-05 | 0.00288585 | intron-variant | TLE1 | GRCh38.p7 | 9:81654081 | GAATACTTCACAATC[A/C]GTTCAGAAAGGTAAA | 7088 |
rs200474319 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665876 | CATTTTTTTTTTTTT[A/T]AAGAATTCAGTTGCA | 7088 |
rs200549454 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602845 | CTGTTAAAAAAAAAA[-/A]CGAGTTAAATGGGGA | 7088 |
rs200582982 | in-del | -/GAAA | | | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583259 | AGAGAGAGAGAGAAC[-/GAAA]GAAAGAAAGAGAGAA | 7088 |
rs200589432 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634485 | GGAAAGGGGAAAAAA[-/T]GCGATTAGTGCTTTC | 7088 |
rs200596594 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603971 | TGGGCCACTACACTC[C/G]AGCCTGGATGACAGA | 7088 |
rs200599120 | in-del | -/G | 0.0640965 | 0.167152 | intron-variant | TLE1 | GRCh38.p7 | 9:81677241 | GACTCGTCTTCCCCC[-/G]CCCCAAAAAAAAGAC | 7088 |
rs200600549 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587455 | TAACAGAGAACACAC[C/T]TTAACCTACAGGATT | 7088 |
rs200607876 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644956 | CCGATATCGCACCAC[C/T]GCACACTGCACTCCA | 7088 |
rs200658295 | snp | G/T | 3.33084e-05 | 0.00408082 | intron-variant | TLE1 | GRCh38.p7 | 9:81613546 | TTAAACAAATTAAAT[G/T]AGTATTATTTTTAAT | 7088 |
rs200661439 | snp | C/T | 0.00995003 | 0.0698284 | intron-variant | TLE1 | GRCh38.p7 | 9:81660171 | AAATACTGTGACACA[C/T]TTCTTTGCCGTACCT | 7088 |
rs200665798 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634479 | GAGGGAGGAAAGGGG[A/G]AAAAATGCGATTAGT | 7088 |
rs200667628 | snp | A/G | 0.00136679 | 0.026106 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687456 | GCGACCAGCGAGGGG[A/G]ACCGAGGGACGGGAA | 7088 |
rs200682167 | in-del | -/TG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637538 | ATGGGTAACTTCCAC[-/TG]CTCTACCCTAATCTG | 7088 |
rs200684286 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636828 | GCCAAGATGGTGAAA[A/C]CCCGTCTCTACTAAA | 7088 |
rs200747710 | in-del | -/AAAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681561 | TCGCGCAAAAAAAAA[-/AAAG]AAAAAAAATTCTTCA | 7088 |
rs200821223 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584796 | ACCCTCAAATATAGA[A/G]ATCAATGAAGAATGT | 7088 |
rs200826417 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670725 | ATCAGAAAAAAAAAA[A/T]TTAAAAAAAAAAAAT | 7088 |
rs200879309 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81613378 | AGGCGATGCTGTACC[C/T]GCTTGGTTAACGAGG | 7088 |
rs200886715 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643242 | TGTTTTTTGTTTTTT[-/G]GGTTTTTTTTTTTGA | 7088 |
rs200888219 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81615479 | TGAGGCGGGTGGATC[-/A]AAAGAGGTCAGGAGT | 7088 |
rs200896348 | snp | C/T | 6.87829e-05 | 0.00586402 | missense, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587695 | CCTGGGAGGTGAAGT[C/T]GTGCTGCTGCAGCTG | 7088 |
rs200959044 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617134 | ATTACTAGTTAATGC[-/AA]AAAAAAAAAAAAAAA | 7088 |
rs200982473 | snp | C/G | 0.00199806 | 0.0315443 | missense | TLE1 | GRCh38.p7 | 9:81591016 | GAGTGCAGCCATCGG[C/G]TAGCAATTTACAGGA | 7088 |
rs201024387 | snp | A/C | 0.00199808 | 0.0315443 | missense | TLE1 | GRCh38.p7 | 9:81590836 | TGTGCAGATCCCACA[A/C]AGCGATGTTGCCGTC | 7088 |
rs201045494 | snp | C/G | 1.64906e-05 | 0.00287142 | missense | TLE1 | GRCh38.p7 | 9:81620539 | CTCTTAGACTGTCTG[C/G]GACCAGGAGGGAATT | 7088 |
rs201075687 | in-del | -/AAAC | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81646275 | TTGTGCTCTCAGTAA[-/AAAC]AAACAAACAAATTTA | 7088 |
rs201086026 | snp | A/G | 1.76428e-05 | 0.00297003 | missense | TLE1 | GRCh38.p7 | 9:81610220 | CTTTGAGGTACTTAC[A/G]GTTTCCCCCCAGGGA | 7088 |
rs201099886 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667406 | AAAAAAAAAAAAAAA[C/T]AAGCAAAAATCAAGT | 7088 |
rs201140985 | snp | C/G/T | 6.64809e-05 | 0.00576513 | missense | TLE1 | GRCh38.p7 | 9:81591013 | TGAGAGTGCAGCCAT[C/G/T]GGGTAGCAATTTACA | 7088 |
rs201222641 | snp | A/G | 1.6625e-05 | 0.00288309 | intron-variant | TLE1 | GRCh38.p7 | 9:81652329 | CATTAGCAACAGCCA[A/G]AAACTTCACTGTATA | 7088 |
rs201239828 | in-del | -/TTTC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613903 | GAAGACCCCTTTTCT[-/TTTC]TTTTTTTTTTTTTTT | 7088 |
rs201258308 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625594 | CACAATTATGAAACC[A/C]CATACCTTCATGTAA | 7088 |
rs201265824 | snp | A/G | 1.64996e-05 | 0.0028722 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585572 | GTACTTGTCAGGCTT[A/G]TTCACGTGCAGCACC | 7088 |
rs201268781 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661222 | TATATATATATATAT[C/T]TTTTTTTCAAGATAT | 7088 |
rs201274756 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679313 | TCTTCACTTTTTTTT[C/T]TTTTTTTTTCCCCTG | 7088 |
rs201385680 | snp | A/G | 0.0029955 | 0.0385847 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634181 | CACTAGACAGCGCAA[A/G]AAGGCCGGCACTGCC | 7088 |
rs201387236 | snp | G/T | 3.32226e-05 | 0.00407556 | intron-variant | TLE1 | GRCh38.p7 | 9:81654073 | AATGTTTAGAATACT[G/T]CACAATCAGTTCAGA | 7088 |
rs201391449 | snp | A/C | 0.000122319 | 0.00781949 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81610225 | AGGTACTTACGGTTT[A/C]CCCCCAGGGATTCCT | 7088 |
rs201398319 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662715 | AAAAAAAAAATTAGC[-/A]AAAGTGGCCAAGCAC | 7088 |
rs201420106 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643324 | TCACGGCAACCTCCA[C/T]CTCCTGGGTTCAAGC | 7088 |
rs201447035 | in-del | -/T | | | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689661 | CGGGAGGTTGGGGGG[-/T]GGGGGGGGGGCAGAA | 7088 |
rs201465652 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661756 | ATGACAACCTTAAAT[-/C]CCCCCCCCCAAAAAA | 7088 |
rs201473724 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684164 | AAAAAAAAAAAAAAA[-/G]ATTAAACCGCCTAGG | 7088 |
rs201496962 | snp | A/G | 0.000230711 | 0.0107379 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81620522 | TCTGCGTTTATCTGT[A/G]CCTCTTAGACTGTCT | 7088 |
rs201511935 | snp | A/G | 0.00214224 | 0.0326578 | intron-variant | TLE1 | GRCh38.p7 | 9:81584436 | GGATCTAGGTGAGGA[A/G]TACTTACTCACCTGG | 7088 |
rs201550866 | snp | C/T | 7.0399e-05 | 0.0059325 | intron-variant | TLE1 | GRCh38.p7 | 9:81591091 | GCTATAATGAATTAC[C/T]GAGCAATCATAGCAC | 7088 |
rs201559857 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636139 | ATTCATAGCATTCTT[A/G]GAAAGTATAAACTAC | 7088 |
rs201562294 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81591008 | CACTATGAGAGTGCA[A/G]CCATCGGGTAGCAAT | 7088 |
rs201576970 | snp | C/T | 0.000399281 | 0.0141238 | missense | TLE1 | GRCh38.p7 | 9:81591012 | ATGAGAGTGCAGCCA[C/T]CGGGTAGCAATTTAC | 7088 |
rs201632653 | in-del | -/AAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617134 | ATTACTAGTTAATGC[-/AAA]AAAAAAAAAAAAAAA | 7088 |
rs201636079 | snp | A/G | 0.0096295 | 0.068717 | missense | TLE1 | GRCh38.p7 | 9:81620452 | TTACATAGTGGCTGG[A/G]GTCCTTATCATCCAC | 7088 |
rs201852120 | in-del | -/TG | 0.0150606 | 0.0854603 | intron-variant | TLE1 | GRCh38.p7 | 9:81668932 | CAATTTATATGCTCC[-/TG]TGTGTTTTTAGAAAA | 7088 |
rs201867558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81584335 | AATGGACATGTGTTT[A/C]ATGTGGAACAACGGT | 7088 |
rs201869564 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676829 | CAGTCTCTGAGCAGT[A/G]GGGACACTGGGCAAG | 7088 |
rs201873489 | snp | A/G | 0.001998 | 0.0315437 | missense | TLE1 | GRCh38.p7 | 9:81590922 | GCGGGGGCCGAGGAC[A/G]TCAGCTCCGCCTTGA | 7088 |
rs201947638 | in-del | -/AT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625596 | CAATTATGAAACCAC[-/AT]ACCTTCATGTAAGAA | 7088 |
rs202058783 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637644 | CTACAATGAAAGTTT[C/T]TTTTTTTTTTTTTTT | 7088 |
rs202165777 | in-del | -/AG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679996 | ATTTACTAAAGAAAC[-/AG]ATTTTCTTTCTGTTT | 7088 |
rs202210085 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684163 | AAAAAAAAAAAAAAA[-/A]GATTAAACCGCCTAG | 7088 |
rs202220952 | snp | C/G/T | 3.30875e-05 | 0.00406729 | intron-variant | TLE1 | GRCh38.p7 | 9:81653939 | AACAGAGAAGCAACA[C/G/T]AATTGCACTTTAACA | 7088 |
rs202222787 | snp | A/G | 4.96151e-05 | 0.00498047 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593247 | AGGCTGCATCTGACC[A/G]TCTGCAGTAACGTGG | 7088 |
rs202236753 | snp | C/T | 0.000660807 | 0.018165 | missense | TLE1 | GRCh38.p7 | 9:81585616 | TCTCCATGCCCACTG[C/T]CAGCCACTCCCCGGT | 7088 |
rs207470317 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627962 | GGTGGCTCACGCCTG[C/T]AATCTCAGCACTTTG | 7088 |
rs367552658 | snp | A/G | 0.000117537 | 0.00766517 | intron-variant | TLE1 | GRCh38.p7 | 9:81590789 | AACCCCTCCTTAGAC[A/G]ACCATCTTTGCTCAC | 7088 |
rs367558027 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682044 | TGAGGTCAGGAGTTC[A/G]AAACCAGCCTGCGAA | 7088 |
rs367599755 | snp | A/C | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587836 | GGAATTGCCTGATAA[A/C]ACAAACCAGATTGAA | 7088 |
rs367649861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81625370 | GAATGGCAGATCTTC[C/T]GATATTACAGCCTGT | 7088 |
rs367652693 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668150 | AGCAGCCTGGGCGAC[A/G]GAACAAGACTGCATC | 7088 |
rs367687065 | in-del | -/TT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632256 | ATTTTCCAGAGAAAT[-/TT]ATAGGACAAGAATTT | 7088 |
rs367694550 | snp | A/G | 1.92162e-05 | 0.00309963 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688205 | CCCCACCACCACCCA[A/G]CCGCGCCTCACCGGG | 7088 |
rs367720144 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81585747 | GGAAATAGCAAGAAT[C/G/T]GGGGGAAGTAATCAG | 7088 |
rs367727653 | in-del | -/TA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623617 | AACCCCATCTGTACT[-/TA]AAAAAAAAAAAAAAA | 7088 |
rs367730925 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601879 | CCTGTCTCCCACCTA[C/T]TCAAGGCAACGAACA | 7088 |
rs367741429 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653004 | CTCACCCCACACCTC[C/T]CAACTCCCAACTCCA | 7088 |
rs367741936 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621124 | TCCTCGCCAATAGCA[A/C]TGAAATTTAAGATCT | 7088 |
rs367755739 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618517 | ATGCAATTCACTAGT[A/G]ACAACTTCAAATTAC | 7088 |
rs367759490 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638775 | GATTCCAGGTGCACA[A/C]CACCACGCCCAGCTA | 7088 |
rs367766171 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653238 | GCCAACCAGGATACC[C/T]AGTATTCCAACTCCT | 7088 |
rs367779642 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688928 | CGGAGGGCGCGCCGG[A/G]AGGCGGCTCGGCACG | 7088 |
rs367782437 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585432 | CCAGATTATGATCTC[C/T]ACCATATTTTTTTAA | 7088 |
rs367785441 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81600020 | GGAAGTATTCCAGCC[A/G]AAGTCAACATTTAAG | 7088 |
rs367859538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678508 | ATGCCTGGCTTGCAA[C/T]TTAGTAATTATTAAA | 7088 |
rs367862048 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649407 | AAGCTGGATGTCCTT[A/G]AGATGATTTACTTTT | 7088 |
rs367883197 | in-del | -/AGAAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655869 | AAAAAAAAAAAAAAA[-/AGAAAA]GAAAAGAACAAAACC | 7088 |
rs367897311 | snp | A/G | 0.00239568 | 0.0345268 | intron-variant | TLE1 | GRCh38.p7 | 9:81634329 | GTGGTGAGAGAGAAA[A/G]AGGAGGAGGAGGAGG | 7088 |
rs367939465 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81608035 | GAAATTCAATTTTAT[A/C]TCATGCTGGTGGTTT | 7088 |
rs368119508 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591962 | CCATCTGCAACAGCA[A/G]AGTGCAGGCAGACAC | 7088 |
rs368143579 | snp | C/T | 6.90429e-05 | 0.00587509 | intron-variant | TLE1 | GRCh38.p7 | 9:81590756 | GCAGAGGTGATAGGC[C/T]CAGCTGCTAAAGAAG | 7088 |
rs368160896 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591123 | TGTTCTCTAATGGCT[-/G]GTCTTGGTTTTTTGA | 7088 |
rs368162519 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81652268 | GGCACGTTCAACAGC[C/G]TGGGCCACCTGTTGT | 7088 |
rs368164926 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625595 | ACAATTATGAAACCA[C/T]ATACCTTCATGTAAG | 7088 |
rs368173587 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TLE1 | GRCh38.p7 | 9:81584402 | CCTGGCTTCAGAGGC[A/G]ACACTGTGGTCAAAC | 7088 |
rs368196844 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625127 | AGATGATTAGATGAG[A/G]TGCAAGAACACAGAA | 7088 |
rs368206711 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598077 | AAGCCCCGCTGCCTA[C/T]GGACTTGGCACTCTG | 7088 |
rs368220859 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633168 | AGAGCGAACAGTCAT[A/G]TAAGAAAAAGAAATT | 7088 |
rs368244066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81591316 | GGTATGAGGTACAGG[C/T]GTACACATAGTTCCC | 7088 |
rs368249918 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621766 | CATGGACCCCACCAT[A/G]GGAGGGTTGTCTCCA | 7088 |
rs368266481 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585099 | ACTGTAGAGTAGAGT[C/G]TAACTAAGTGTCTGC | 7088 |
rs368295077 | snp | G/T | 0.450609 | 0.149185 | intron-variant | TLE1 | GRCh38.p7 | 9:81639575 | TGATTAGTAAAAGTT[G/T]TTTTTTTTTTTTGTT | 7088 |
rs368313583 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611426 | CTTCTGTGAACCACT[C/T]GAATCATTTCATCGC | 7088 |
rs368337973 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659166 | GCCCACCTCAGCCTC[C/T]CAAAGTGGTGGGATT | 7088 |
rs368357524 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682328 | AAGCTTCAATAGATG[C/T]GTGGCCTTGAGCAAG | 7088 |
rs368364547 | snp | A/C | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587131 | TATTTCAAAAGTCTG[A/C]AAATCTAGTCAGCCA | 7088 |
rs368374703 | snp | C/T | 1.65141e-05 | 0.00287346 | intron-variant | TLE1 | GRCh38.p7 | 9:81616608 | ATAACATTATTCAAA[C/T]CATTCTGAAGACAAA | 7088 |
rs368394601 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671229 | AAAACTAATGTATTC[C/T]TAGGCTGGGTATGGT | 7088 |
rs368407658 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81654706 | GCAAGTTCATTCAAG[C/T]GGGTGTCAGAAGCCA | 7088 |
rs368421825 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689492 | CTGCTGCTGCTGCTT[C/G]TGCAGCCGCCGCTCC | 7088 |
rs368456981 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587929 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 7088 |
rs368595624 | snp | C/T | 3.29598e-05 | 0.00405941 | missense | TLE1 | GRCh38.p7 | 9:81590890 | TGGAATCGGGGCTGA[C/T]GGCCAGGGCGTAGCA | 7088 |
rs368620927 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666533 | TGTAATCCCAGCATT[C/T]TGGGAGGCCGAGGCA | 7088 |
rs368687385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81683157 | GAAGGGAGAGCGGTC[A/G]TCACACTGGAGACAA | 7088 |
rs368698372 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690944 | TAATGCTGAGAGTCT[-/TT]GGTTTTTGTGTATGT | 7088 |
rs368721457 | snp | A/C | 6.69781e-05 | 0.00578659 | intron-variant | TLE1 | GRCh38.p7 | 9:81585469 | TTTTCCATTTGGGCC[A/C]TCAACGGCCTCCAGT | 7088 |
rs368768368 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650588 | ATTTGATCTCTGAAA[C/T]AAAGCAATTCATTAC | 7088 |
rs368778423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81636687 | AGACCAAACATACTC[C/T]GGTAATATTTAGATA | 7088 |
rs368787611 | snp | C/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688124 | AGGGCGAGAAGGTCC[C/G]CCGGGCCTCAGAAGC | 7088 |
rs368866357 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623265 | TTGCTTATGGCTCCA[G/T]GGTAGAATACAGTCA | 7088 |
rs368921248 | snp | C/T | 2.13472e-05 | 0.00326698 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587633 | GAGGAGGAAGACACA[C/T]CCCAGCCACCTCCCA | 7088 |
rs368929494 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589462 | TAGCCACCTGTGAGT[C/G]GTCCAGAGAAAGATT | 7088 |
rs368961777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81666892 | TGAGAGCAAGGTAAG[A/G]GGATCACCGCAGAGC | 7088 |
rs368970037 | snp | C/T | | | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611802 | GGCCACCACGGCGGC[C/T]GCGGCGGCTGCGGCG | 7088 |
rs369047659 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81626344 | ACAATTAGGTAACGA[C/T]GCACCCCATCACATC | 7088 |
rs369058379 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622130 | TGCAAAGTGCTAACA[C/T]GCCCTCTGAAAAGCT | 7088 |
rs369105538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680453 | ATGTTGTTCCTTGAA[A/G]ATTTTGGGGGCATTC | 7088 |
rs369138200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599764 | CAGAACAGGGTATAA[C/T]TCCCACCTTATTTGG | 7088 |
rs369143469 | snp | A/G | 1.65701e-05 | 0.00287833 | intron-variant | TLE1 | GRCh38.p7 | 9:81613364 | CAAAGCACAACAAGA[A/G]GCGATGCTGTACCCG | 7088 |
rs369159070 | in-del | -/GAAGAAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615122 | AAAAAAAAAAAAAAA[-/GAAGAAG]AAGAAGAAGGCAATG | 7088 |
rs369184952 | in-del | -/C | | | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689778 | CGGGGCGTTCTCCCT[-/C]CCCCCCCTCCTCTCG | 7088 |
rs369191615 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671369 | AGAAAAATGAAGGCC[A/C/G]GGCATGGTGGCTCAT | 7088 |
rs369268138 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626398 | TGGTGTCAATCAAGC[C/T]ATCACCCTGCGCTGC | 7088 |
rs369268527 | snp | C/T | 1.64893e-05 | 0.0028713 | intron-variant | TLE1 | GRCh38.p7 | 9:81633402 | ACGCACAGACATGCC[C/T]GTTCAGACACAGAGG | 7088 |
rs369268791 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688979 | GTGTTCTCCGCGGTT[A/G]CACAAACCCTCCGGG | 7088 |
rs369288148 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81620137 | CACCAAGGGAGGCGG[A/G]GGGCCCGGGGGACTC | 7088 |
rs369318555 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592970 | CCACACAGCTATTTC[C/T]TTATTGAATCTCCAG | 7088 |
rs369331200 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590942 | CTCCGCCTTGATGCG[C/T]GGGGTTGGAGCCGCC | 7088 |
rs369337828 | snp | A/G | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589691 | GACAGACGTTATGAG[A/G]ACTAAGTGGAGGAAT | 7088 |
rs369345680 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688313 | CAACTTTAATCCCGC[A/C]GAGGAAAATTAAGCC | 7088 |
rs369358950 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81651309 | AGTGTGGAAGGGGAC[A/G]AACACATGAGAACCA | 7088 |
rs369474073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81592086 | GAACATGGCCGGGCG[C/T]GGTGGCTCACGCCTA | 7088 |
rs369485854 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612529 | GTTTTTTAAGGGCTG[C/G]AGTCGCAGAGAAACC | 7088 |
rs369509308 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605299 | AGTGAGATGAGTGCA[C/G]TCATCGAGAGTGAGC | 7088 |
rs369514077 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81610370 | ATCAATACTGTTCAT[A/T]AGAAACTCACAGATC | 7088 |
rs369565989 | snp | C/T | 2.28809e-05 | 0.0033823 | missense | TLE1 | GRCh38.p7 | 9:81611785 | ATGGGGGAGCGCCCG[C/T]AGGCCACCACGGCGG | 7088 |
rs369612362 | in-del | -/GAG | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587250 | AATGAACTTTCAGAG[-/GAG]CTGTGACTTTTCTCT | 7088 |
rs369616474 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641916 | AATCCCAGCTACTCA[C/G]GAGGTTGAGGCAGGA | 7088 |
rs369620985 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618639 | TCTGTTTTCTCTTGG[G/T]AAAGCCCACAGCAAA | 7088 |
rs369638928 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593633 | GTATCTTGTGTAATT[G/T]TATGATTTCTTAGTA | 7088 |
rs369658863 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636574 | AACTACAGGGTGGAG[A/G]ATGCCACCCTCTCAC | 7088 |
rs369666102 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668221 | AGTTGTGGTGGGCAA[C/G]GGTAGGGATTAAAAT | 7088 |
rs369676835 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684173 | AAAAAAGATTAAACC[A/G]CCTAGGCCAAGTTTA | 7088 |
rs369707622 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666895 | GAGCAAGGTAAGAGG[A/T]TCACCGCAGAGCAGG | 7088 |
rs369745595 | in-del | -/TAC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615542 | CATCTCTACTAAAAA[-/TAC]AAAAAAAAAAAAAAA | 7088 |
rs369781798 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596566 | ACTTAACTTTCTCTA[C/T]TGGTTGAGGAACTAG | 7088 |
rs369838499 | snp | C/T | 3.29815e-05 | 0.00406075 | intron-variant | TLE1 | GRCh38.p7 | 9:81633372 | CTCTCTGTCTGCTCC[C/T]GAGGTTACCAAGAAA | 7088 |
rs369865514 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662233 | AAGAGAACAGTTAAA[C/T]ACGCTACACACCAAC | 7088 |
rs369874713 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670176 | AGTCCTCCTGAGTAA[C/T]AGACTTGGAAAAGTA | 7088 |
rs369909896 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81681824 | CTAACTTTTAGAACA[C/T]ACATTCAGTCCTGAC | 7088 |
rs369913450 | snp | A/G | 8.23879e-05 | 0.00641772 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616081 | CAGGCGATTTTTGTC[A/G]ATTCCATTTTCCCGG | 7088 |
rs369958282 | snp | A/G | 1.67795e-05 | 0.00289646 | intron-variant | TLE1 | GRCh38.p7 | 9:81613560 | TGAGTATTATTTTTA[A/G]TCCAAGCCATATTAC | 7088 |
rs370074748 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640841 | AACTGGGAAGGACAC[C/T]CAGTATGAAAACACA | 7088 |
rs370127125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587146 | CAAATCTAGTCAGCC[A/G]CCAGTTCATTTTTTA | 7088 |
rs370165437 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624463 | AGACACCTCTTCCTA[C/G]AGTCTATACTTTGAA | 7088 |
rs370206862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81591591 | TCTTTCCATCAAAAC[C/T]GACACATATGAAGGG | 7088 |
rs370258718 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609512 | TCACACTTCTAATTA[C/T]TAACATTATGAAAAT | 7088 |
rs370336465 | snp | A/G | 0.000115347 | 0.00759343 | utr-variant-3-prime | TLE1 | GRCh38.p7 | 9:81584179 | AATTCAACTATAAAC[A/G]TTAAACCACATAATG | 7088 |
rs370352587 | snp | C/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587930 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 7088 |
rs370372756 | snp | A/C/T | 9.89033e-05 | 0.00703161 | intron-variant | TLE1 | GRCh38.p7 | 9:81616720 | AAAAAGAAACATTAA[A/C/T]GCCATTTACTAAAAG | 7088 |
rs370379670 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661631 | AGTGGAGTGTTGGTA[A/G]GAAGTGTCTGGCAAC | 7088 |
rs370398751 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628906 | GTTATAGTCTCTCCC[C/T]AGAATTCTGCAAAAG | 7088 |
rs370411352 | in-del | -/AGA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683915 | CCTACATGATAAAGA[-/AGA]GGTCATCCCGCCACA | 7088 |
rs370422916 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602997 | GTTGGGAAACCCATC[C/T]TGTCATCTTAACACC | 7088 |
rs370440694 | snp | A/G | 0.000446648 | 0.0149374 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688260 | CTGGCGGCGGCCGGG[A/G]CTCTGTTCCCCGGCA | 7088 |
rs370440918 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583283 | GAGAGAAAGGGAAAG[A/T]GAAAGGGAAAAGGAA | 7088 |
rs370449737 | in-del | -/TC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632236 | CCCCCCAATCCCCTC[-/TC]AACATTTTCCAGAGA | 7088 |
rs370478670 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81584686 | TAATCTGGGCTCCTC[A/C]GTGATTTATCAGTGA | 7088 |
rs370486779 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81595063 | CCTTAATGTTACTCT[A/T]AATTTGAATGAATAA | 7088 |
rs370497042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591629 | GTGGGGGGCCCTCAT[A/G]TGATCAACTCCTGAA | 7088 |
rs370510578 | snp | A/G | 0.000275962 | 0.0117433 | intron-variant | TLE1 | GRCh38.p7 | 9:81634353 | GAGGAGGAGGTAGTG[A/G]TGACAGTGATGGCGA | 7088 |
rs370517305 | snp | C/T | 7.72648e-05 | 0.00621502 | intron-variant | TLE1 | GRCh38.p7 | 9:81593287 | GCACTTTTGGAAAAA[C/T]GATTGGAGAGAAGAC | 7088 |
rs370530269 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655404 | AAAAACCTTTGCTCC[A/G]CTCCACATCCACAGC | 7088 |
rs370556228 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662038 | TAAGAATTTATCCTA[A/G]GGAAATAGTTCAAAT | 7088 |
rs370564897 | snp | A/G | 0.000111286 | 0.0074586 | intron-variant | TLE1 | GRCh38.p7 | 9:81611979 | AAGGAAACACAAGCC[A/G]CACATCATTCAACTG | 7088 |
rs370578171 | in-del | -/T | 0.0100098 | 0.0700334 | intron-variant | TLE1 | GRCh38.p7 | 9:81633588 | CAAAGCCTATTTTTT[-/T]ATTTCTTGACAGAAT | 7088 |
rs370633706 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656112 | GAAGCCCGTGCATGA[C/T]CTTGCTTTAGCCAGC | 7088 |
rs370651922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687186 | GAAGAACCAGGAAAG[A/G]GGGTAACTTGAATGA | 7088 |
rs370656084 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642036 | TCCAAAAAAAAAGAA[A/G]GAAAGAAAGAAATGT | 7088 |
rs370676690 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689001 | CCCTCCGGGCCCGAC[A/G]GGGCTACTCCACCGA | 7088 |
rs370695976 | snp | A/C/G | 0.000344961 | 0.0131289 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687460 | CCAGCGAGGGGGACC[A/C/G]AGGGACGGGAATGCG | 7088 |
rs370774622 | snp | C/T | 0.000245058 | 0.0110666 | intron-variant | TLE1 | GRCh38.p7 | 9:81611754 | CCAACCACAGCCCAC[C/T]CGACAGCGGCCTACC | 7088 |
rs370781251 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632474 | TAAATGTTCAGTATC[C/T]CTTTTTTTTTTTTTT | 7088 |
rs370783883 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647842 | ATGTAAATATTCCTA[C/T]GTGGATTACCAAAAA | 7088 |
rs370791370 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587067 | GTCTACATTCAGACA[C/T]TGGACATCAAAATAC | 7088 |
rs370794848 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669620 | CCACCCTCCCCCCCC[-/C]ACACCAAAAGACATG | 7088 |
rs370796908 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615214 | AGTGCCTGTAATCCC[A/C]GCTACTGGGGAGGCT | 7088 |
rs370837419 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637002 | GGGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 7088 |
rs370867475 | snp | A/G | 9.25112e-05 | 0.00680052 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634236 | CTGAAGTCCCGAAGG[A/G]TGAGGCGTAAGGGGA | 7088 |
rs370898444 | snp | C/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587228 | GCTCTCTGGTGCGGG[C/G]TAAATAAATGAACTT | 7088 |
rs370902640 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TLE1 | GRCh38.p7 | 9:81607056 | CAGGGAGACCCAGTG[C/T]CTCTAAAAAAAAAAA | 7088 |
rs370904391 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688549 | GGCAGCGCTCCAACC[C/G]CCGGCCTCAGCTGCC | 7088 |
rs370905748 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660341 | GACAAAGGCTGTTCA[-/C]AAAAAAAAAAAAACA | 7088 |
rs370908675 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629975 | AAATCTTTAACTAGC[A/G]AATTAATTTCTGCCA | 7088 |
rs370947368 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690444 | CCCCACCCACCCCCT[A/T]TGCACCCAAAGTGGT | 7088 |
rs370967541 | in-del | -/A/AA | 0.338069 | 0.233974 | intron-variant | TLE1 | GRCh38.p7 | 9:81670727 | AGAAAAAAAAAAATT[-/A/AA]AAAAAAAAAAAATCA | 7088 |
rs370977206 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81605695 | AGGCAATACCATTCA[G/T]GACATAGGCATGGGC | 7088 |
rs371010115 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81652201 | TAGGAGGTAGACCTG[A/G]TAGGCCACGTACCCC | 7088 |
rs371027999 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673060 | GGCAGATTACTTGAG[A/G]TCAGGAGTTTGTGAC | 7088 |
rs371036630 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603451 | ACCTCTCTCTTTCTA[G/T]ACAAAAACAGGCCAT | 7088 |
rs371043726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638371 | CATTTCTAAGATAAC[A/T]TATTTATTTAAATGA | 7088 |
rs371055340 | snp | A/C/G | 0.000117018 | 0.00764836 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687318 | GACCACTCGCATGGC[A/C/G]CGGCCGGACACGCAC | 7088 |
rs371059393 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688728 | CGGCGGCGGGCGAGG[C/T]GCAGGTGGCGCGGCG | 7088 |
rs371087909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81676490 | GGTTGATACAAAAGC[C/T]TGGACTTTTTATAAA | 7088 |
rs371089248 | snp | A/G | 0.00011536 | 0.00759387 | synonymous-codon, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587789 | GCCATCATTAGAAAT[A/G]TCAATACAGCTGGCT | 7088 |
rs371090700 | in-del | -/A | 0.485731 | 0.0832509 | intron-variant | TLE1 | GRCh38.p7 | 9:81615713 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 7088 |
rs371180154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81632582 | CTGAAAAGGGGCTGA[A/G]TTCTCTCTATTTGCT | 7088 |
rs371248852 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644746 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCAGA | 7088 |
rs371262506 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626361 | CACCCCATCACATCT[G/T]TGTGCCTTCTCCATC | 7088 |
rs371266921 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609138 | CACCCAGGCTGGAGT[A/G]CAGTGGCATGATCTT | 7088 |
rs371279554 | snp | C/T | 0.000102076 | 0.00714334 | intron-variant | TLE1 | GRCh38.p7 | 9:81585689 | GCTCACTCATTATTC[C/T]GCCTGATACACTTAG | 7088 |
rs371308735 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671715 | AACCTCCTTATACTT[A/C]CTCCTTATACTTCCA | 7088 |
rs371313796 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | TLE1 | GRCh38.p7 | 9:81590793 | CCTCCTTAGACGACC[A/G]TCTTTGCTCACCTCA | 7088 |
rs371319269 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611620 | AGGTGAGTGTGTGGC[C/T]GGGAGACTGGGCGTC | 7088 |
rs371373554 | snp | C/G | 3.53632e-05 | 0.0042048 | intron-variant | TLE1 | GRCh38.p7 | 9:81633329 | TGTGTGTGTGTGCAG[C/G]AGGCGTTTGAGTACT | 7088 |
rs371415777 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592645 | AAATATTTACTATTC[C/T]ATATTTATCTAAAGG | 7088 |
rs371419869 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81635718 | CATGCCAGATCTTCA[A/G]TCATTTCTACCCAGC | 7088 |
rs371423047 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616756 | AATAGGTTTGAGGCA[C/T]AGTTAGATTTCTTTC | 7088 |
rs371427995 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648858 | AAAACGATCCTGATC[C/T]AAAAACTCAAGGTCT | 7088 |
rs371442800 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81668208 | AAAGGAAGTTGGAAG[C/T]TGTGGTGGGCAAGGG | 7088 |
rs371481803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81596280 | GTCAGAAGCTGTGAA[C/T]ACTCATCCGTCCCAC | 7088 |
rs371483068 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585230 | CACCCCTCTTCAGAG[G/T]AGAAACTCATTGTCG | 7088 |
rs371507322 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | TLE1 | GRCh38.p7 | 9:81584539 | CCTAGAATTAGCAAA[C/G]GAATATCTAGTTTTC | 7088 |
rs371532796 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631449 | TCCACAATTCTGATA[C/G]CAGTAAGTTATAGGA | 7088 |
rs371538144 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607437 | ACAGCTCTGCTCACC[C/T]GCCTTCCCCCACTGC | 7088 |
rs371558270 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665241 | TTCATTTAAGTTATT[C/G]CACCCATGGCAATGT | 7088 |
rs371569304 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646252 | TTCTGCATTTGTCAG[A/G]CGCCTAGTTGTGCTC | 7088 |
rs371602270 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81668660 | GGACAGAATCTATTC[-/AG]AGTTACAGGGACTGA | 7088 |
rs371607860 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585003 | ATCCATCCATCCATC[C/T]ATGCATACTGTGAAC | 7088 |
rs371624418 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585855 | CTGGAAACATTTGAA[C/T]CCCTCTGTCTTTTGG | 7088 |
rs371722343 | snp | A/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588664 | TAGCAGAGCTGCTGA[A/G]GGGAGGTCAGTGTAA | 7088 |
rs371791006 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81594668 | TATGCACTGCTTCCT[-/C]CTTCCCATTACCCTC | 7088 |
rs371805789 | in-del | -/AG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606802 | CATATATATATATAT[-/AG]AGAGAGAGAGGCAGT | 7088 |
rs371864767 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81652455 | CATAGATAGGGAAAG[-/A]AAAACTGAGAATGGC | 7088 |
rs371888008 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592130 | TTGGAAGGCCAAGGC[A/G]GGCGGATCACAAGGT | 7088 |
rs371891089 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81604298 | TGTGAAAGTGTGGAT[-/G]GAAAGGAAGTGACAG | 7088 |
rs371923296 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680304 | GGCCACTCCCCACAG[A/G]ACAGGTAACCAAAGG | 7088 |
rs371930193 | snp | A/G | 9.89511e-05 | 0.00703319 | missense | TLE1 | GRCh38.p7 | 9:81620544 | AGACTGTCTGGGACC[A/G]GGAGGGAATTACTCT | 7088 |
rs371936084 | in-del | -/TGTGTGTGTGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662362 | TTAGTGTGCCTGTTT[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 7088 |
rs371977224 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | TLE1 | GRCh38.p7 | 9:81621258 | TCATTCGCATATGCC[C/G]AGTAGGAACTGTTGA | 7088 |
rs371977486 | snp | A/G | 0.000360129 | 0.013414 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611892 | GCCGTTCATGCCAGC[A/G]TGGGGGACCATCCCA | 7088 |
rs372013873 | snp | A/G | 0.000131843 | 0.00811815 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590909 | CAGGGCGTAGCAGGC[A/G]GGGGCCGAGGACGTC | 7088 |
rs372055037 | in-del | -/TG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649297 | GTGAGAAATGGGGAC[-/TG]TTAATTCACTCAACA | 7088 |
rs372056637 | snp | A/C | 1.65061e-05 | 0.00287277 | intron-variant | TLE1 | GRCh38.p7 | 9:81584403 | CTGGCTTCAGAGGCG[A/C]CACTGTGGTCAAACT | 7088 |
rs372182960 | snp | C/T | 8.39342e-05 | 0.00647766 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685929 | GCAACTTAATGTAAA[C/T]ATTATGTCACTTGTT | 7088 |
rs372238712 | snp | C/T | 0.00917412 | 0.0671036 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611829 | GGCGCTCATCTGGGG[C/T]GACATGTTGTGTAAA | 7088 |
rs372260929 | snp | G/T | 0.000437904 | 0.0147905 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685775 | TGTTTTTTACACTCT[G/T]CTAACACGTTTGCTA | 7088 |
rs372319030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81683458 | TGCTGGTGATCAGGC[A/G]GCAAAAAGCATCAAT | 7088 |
rs372397051 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629019 | CTCCCTTTTCCAAAT[A/C]GTGATCACACTAGCT | 7088 |
rs372453248 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661738 | AAGTTTCTGAGTCTG[C/T]GAAATGACAACCTTA | 7088 |
rs372522926 | in-del | -/AGATC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628252 | TAACCCCCTCCCTGT[-/AGATC]GAGGCAACCACTACT | 7088 |
rs372525045 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | TLE1 | GRCh38.p7 | 9:81654403 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACCA | 7088 |
rs372529003 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687354 | ATACTGCGCCTGCAG[A/G]AACTGGAATTCCTCT | 7088 |
rs372534909 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639412 | TCATTTGGAAAACTG[C/T]AAGATGTTTTTTTCA | 7088 |
rs372540893 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81643531 | ATGAGCCACCGCACC[C/T]AGCCCTTTGTTTTGT | 7088 |
rs372541774 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680890 | TTAGGGGGAAAAAAA[A/T]TCTCAAAGTGAGAAA | 7088 |
rs372554811 | snp | C/T | 9.88973e-05 | 0.00703128 | missense | TLE1 | GRCh38.p7 | 9:81620487 | CTTTTCTTGATGTCA[C/T]TGGAAAATTCAGGTC | 7088 |
rs372561587 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673686 | ATCCACACAAAGGGA[A/G]GCTGGGAAGGTTGAC | 7088 |
rs372638444 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667449 | TTTCCCTAACACATT[G/T]AAATCTTCAGCCAAT | 7088 |
rs372658613 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649973 | CGGACATAAATTCAT[A/G]TACTAATCCAAAAAT | 7088 |
rs372696198 | snp | A/C/G/T | 0.0111237 | 0.0737856 | intron-variant | TLE1 | GRCh38.p7 | 9:81667723 | TATTCCTGCTCCCCC[A/C/G/T]CAAGCTGAGTGGCTG | 7088 |
rs372701562 | snp | A/G | 0.0130921 | 0.0798413 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688994 | GCACAAACCCTCCGG[A/G]CCCGACGGGGCTACT | 7088 |
rs372729938 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583704 | GTACTAAAGCCTTTA[C/T]TGTAATAAACCAAAT | 7088 |
rs372771789 | in-del | -/T | 0.0486741 | 0.148216 | intron-variant | TLE1 | GRCh38.p7 | 9:81660581 | ACCACACCCGGCTAA[-/T]TTTTTTTTGTATTTT | 7088 |
rs372779300 | in-del | -/TGTGTGTGTGTGTGTGTGTGTGTGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662362 | TTAGTGTGCCTGTTT[-/TGTGTGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 7088 |
rs372793231 | snp | A/G | 0.0138799 | 0.0821421 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689633 | AGCGCGGAGCCGGCG[A/G]GGGACGTGAGCCCGG | 7088 |
rs372805236 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673870 | ACAACTATGTGAGAA[C/T]GGAGTGTGTACCTGT | 7088 |
rs372820784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81674738 | AAATCTCAAGTGACA[A/G]TTGAGAAAGAAATCA | 7088 |
rs372833215 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614110 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 7088 |
rs372848013 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687776 | CCCACGGCGGCGATA[A/G]TGACCCCGGGGACCA | 7088 |
rs372857365 | in-del | -/AAATAAAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666777 | AAGACTCGTCTCACA[-/AAATAAAT]AAATAAATAAATAAA | 7088 |
rs372858373 | snp | A/G | 5.20305e-05 | 0.00510025 | intron-variant | TLE1 | GRCh38.p7 | 9:81591079 | ACATAATTCATTGCT[A/G]TAATGAATTACCGAG | 7088 |
rs372861685 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626802 | GATGCCTTCGTCACC[A/T]CCCTCTCATTTGTAG | 7088 |
rs372862720 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81644163 | TAAAATGATGCAGCC[A/G]CTTTGGAAAACAGTC | 7088 |
rs372871840 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81608983 | AAAGAAAAAGAAAAA[A/G]AAGCAACAACATTTG | 7088 |
rs372886380 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681149 | TGGCCTGAGATGTTG[C/T]TTGCTGAAATATCAC | 7088 |
rs372892005 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660549 | CTCCTGAGTAGCTGG[A/G]ACTACAGGTGCCTGC | 7088 |
rs372912525 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81619609 | CCTGCAAGGGCATCA[C/G]GGACGTAGCCCCATT | 7088 |
rs372941954 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683767 | TTGCTAAGCCAATTA[C/T]ACACAGCATATTATT | 7088 |
rs372989218 | snp | A/G/T | 4.69453e-05 | 0.00484467 | missense, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687421 | AAGGGCTGGCCTGCA[A/G/T]CCTGGTGCGGCGTCT | 7088 |
rs372990411 | snp | C/T | 0.000261814 | 0.0114385 | synonymous-codon, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688232 | CGGGTGCCGGCTCTG[C/T]GGGAACATCGCTCTG | 7088 |
rs372992648 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675987 | TACGGGCGTGAGCCA[C/T]CACACCAGGCCGACC | 7088 |
rs373022797 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664702 | CTCAATCTCTCTTTT[-/T]AATTAAGAAAAAAAA | 7088 |
rs373052141 | in-del | -/TGAAC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678733 | GGCAGGGGAACTGCT[-/TGAAC]CTACATACCTGTAAT | 7088 |
rs373106021 | snp | A/C | 1.64933e-05 | 0.00287165 | missense | TLE1 | GRCh38.p7 | 9:81616107 | CCCGGGGCGAGTGGG[A/C]AGGGCTTGCTCGCGG | 7088 |
rs373201668 | snp | A/G | 3.2963e-05 | 0.00405961 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593217 | TCCGATGAGGGCGTC[A/G]GGGGGAAAAGGGACA | 7088 |
rs373214344 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627319 | AAATTGTTCTCTCAC[-/T]TTTTTTTTTTTAAGA | 7088 |
rs373236831 | snp | A/G | 0.000153988 | 0.00877328 | missense | TLE1 | GRCh38.p7 | 9:81590950 | TGATGCGCGGGGTTG[A/G]AGCCGCCAGGTCCCA | 7088 |
rs373274814 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605348 | TAGGGCTGTTGACTC[C/T]TGTAACAACAAAAAA | 7088 |
rs373293783 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624981 | CAGGGTCAAGTACCC[-/C]TGTACATAAAGGGAG | 7088 |
rs373306042 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689861 | GCCAGCCGCGTCCTC[C/T]CGGGCTTGGTGAGGA | 7088 |
rs373315985 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655699 | CAATGAAAAGGATCA[C/T]AAGAAAAAAACTTAA | 7088 |
rs373362348 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81609250 | CCACCACGCCCAGCT[A/G]ATTTTTGTATTTTTA | 7088 |
rs373385202 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644299 | AGCATTATTCAAAAT[A/G]GCCAATCAGTGGAAA | 7088 |
rs373414375 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681474 | AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 7088 |
rs373415025 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671374 | AATGAAGGCCGGGCA[C/T]GGTGGCTCATACCTG | 7088 |
rs373419880 | snp | A/T | 1.68012e-05 | 0.00289833 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685932 | ACTTAATGTAAACAT[A/T]ATGTCACTTGTTTTA | 7088 |
rs373447774 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609764 | CTTGTTTCCACCAAA[A/G]TAAGAAAAAGGTGGC | 7088 |
rs373450199 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651202 | AGCAATTAACATAAA[C/T]TGATAAATGAGTGAT | 7088 |
rs373459858 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622933 | CCACCTAAAGTCTAC[C/G]CCACCAAAAACAGAC | 7088 |
rs373482291 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657198 | GTGGTGCTTCCTTGA[A/G]TGGGACAAATATTAA | 7088 |
rs373505200 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676915 | TTTAAATGTATACAA[C/T]AGTGTAATACAACAA | 7088 |
rs373511583 | snp | A/G | 0.000106531 | 0.00729756 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611799 | GTAGGCCACCACGGC[A/G]GCCGCGGCGGCTGCG | 7088 |
rs373529882 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616322 | CTGCAAACATGCCAT[-/A]AAAAAAAAACCCCGC | 7088 |
rs373534225 | snp | A/C/T | 0.000173106 | 0.00930196 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634176 | CAGAGCACTAGACAG[A/C/T]GCAAGAAGGCCGGCA | 7088 |
rs373559840 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601595 | AACAGCAGTGCTACA[C/G]TGCCAGAAAAAAAAA | 7088 |
rs373576206 | in-del | -/TA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632136 | GAATGGCAAAACAAT[-/TA]AAGGCTTCCTCCATA | 7088 |
rs373599456 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664600 | GGCACAGTGGCTCAC[A/G]CCTACAATCCCAGCA | 7088 |
rs373619700 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653170 | AAGGTTATGGTGGAA[A/G]AGGCTGTTACAACAA | 7088 |
rs373622654 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591568 | AAAGAACCTGATAAA[-/A]GCAGGCATCTTTCCA | 7088 |
rs373634131 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688846 | CCGGGACGCAAAGGG[G/T]AGCGAGGTTGAAGAC | 7088 |
rs373642117 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662381 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGTGTGTGTGT]TTAAAGGGCCAGGAG | 7088 |
rs373647454 | snp | A/C | 0.000219825 | 0.0104816 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634161 | GTGAGACTGCCCACT[A/C]AGAGCACTAGACAGC | 7088 |
rs373671075 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622151 | CTGAAAAGCTGGGCC[C/G]GGGCAGCAGCTGCTT | 7088 |
rs373697894 | in-del | G/TT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643245 | TTTTTTGTTTTTTGG[G/TT]TTTTTTTTTGACAGA | 7088 |
rs373698223 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669470 | ATCATCAGCTGAAGT[C/T]TGGAACGCAATTTTC | 7088 |
rs373720466 | snp | A/G | 3.42431e-05 | 0.00413768 | intron-variant | TLE1 | GRCh38.p7 | 9:81590773 | AGCTGCTAAAGAAGC[A/G]AACCCCTCCTTAGAC | 7088 |
rs373740168 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595379 | ATTCATGTCCTACAA[G/T]AATTCTAGGCTTTGA | 7088 |
rs373741689 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687875 | AACCGGGGCCGCATT[A/G]ACATGTAAATAGGCG | 7088 |
rs373782434 | snp | C/T | 0.000164736 | 0.0090742 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616021 | AGAAGTGGAACTTGC[C/T]GAGGAGGCCGTGGAA | 7088 |
rs373801253 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81640298 | TCAACATTCAATCAC[-/A]ATTCACTGTCCTTTC | 7088 |
rs373840062 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81627946 | AACCAAGGCTGGGTG[C/T]GGTGGCTCACGCCTG | 7088 |
rs373864615 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661018 | GCCTGTAGTTCCAGC[C/T]ACTCAGAAGCCTGAG | 7088 |
rs373880981 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688658 | AACAAATCCAGACGG[A/G]CTGCTTTTCTTTGCT | 7088 |
rs373883513 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632101 | TCTCAAAAAAAAAAA[-/A]GACTATCTATAGGAA | 7088 |
rs373952910 | in-del | -/CT | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81638956 | TGAAGCAAAGTCTCA[-/CT]CTGTTACCCAGGCTG | 7088 |
rs373962087 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81666838 | CTGTGTAAATAAAGA[C/T]AAAGGCCTGAAGCAC | 7088 |
rs373978146 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TLE1 | GRCh38.p7 | 9:81678249 | GTCTTGCTTGTGTCA[C/T]ACAGTCTAGAGTACA | 7088 |
rs373984023 | snp | C/T | 5.48712e-05 | 0.00523761 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634262 | GGGGAACTGGGGGTC[C/T]GTGGCCATGAGAAAG | 7088 |
rs374005785 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668267 | CAGAAAAAGAACCTG[G/T]GAACAGTTAACAGTC | 7088 |
rs374041308 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621658 | CAACAGGAGCAAATA[C/T]TTTATGGTATCTTTT | 7088 |
rs374088115 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614779 | TTCCCCTGGGGCCTC[C/T]TTTGTGCATCACTGA | 7088 |
rs374139716 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TLE1 | GRCh38.p7 | 9:81632723 | AACATGAACTCTACG[C/T]ACACAGCCCTGTCCA | 7088 |
rs374163627 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667046 | TCACTTGTTCGGAGT[A/G]ATCCTTGGTTTGGAG | 7088 |
rs374197216 | in-del | -/CTAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632108 | AAAAAAAAAGACTAT[-/CTAT]AGGAACCCTGGAATG | 7088 |
rs374208947 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677244 | TCGTCTTCCCCCCCC[-/G]CAAAAAAAAGACCTT | 7088 |
rs374215758 | snp | A/G | 1.64808e-05 | 0.00287057 | missense | TLE1 | GRCh38.p7 | 9:81620512 | CAGGTCCATTTCTGC[A/G]TTTATCTGTGCCTCT | 7088 |
rs374256951 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594380 | AGTTCATGTCCCTTG[A/C]AGGGACATGGATGAA | 7088 |
rs374270718 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81632983 | ATAAAAATGAATATT[C/T]TTTTAAACTACAGTC | 7088 |
rs374286064 | snp | A/G | 3.81658e-05 | 0.00436823 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587664 | GACTCCAGGGCAGGC[A/G]GAAGCCACTCAGTCA | 7088 |
rs374286795 | snp | C/G | 4.94246e-05 | 0.0049709 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81584285 | GATGTCACAGCTAAG[C/G]ACTGACGAGGACTCT | 7088 |
rs374301769 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81638600 | ATAGCCAAAACCCAA[C/T]AGCTCTGCCAATCAG | 7088 |
rs374444332 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639588 | TGTTTTTTTTTTTTG[-/T]TTTTTTTTTTTTTTG | 7088 |
rs374490010 | snp | A/C | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588048 | GTTTTCCACGATCCA[A/C]GTGCTAAAGAAATGG | 7088 |
rs374497497 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TLE1 | GRCh38.p7 | 9:81613976 | GCAGTGGCGCAATCT[C/T]GGCCTACTACAAGCT | 7088 |
rs374501607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620180 | GGGCCCTGAGCAACC[A/G]CACAGCCCACAAAGT | 7088 |
rs374504106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81600196 | ATATATTGCTATTTC[A/G]AAGCTAAACTAAAAA | 7088 |
rs374517134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678576 | TTCCAGCACTTTGGG[A/G]GGCTGAGGCACGTGG | 7088 |
rs374521760 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647459 | CATTCATGCACAACA[A/G]CTTAATGGCAGGAGC | 7088 |
rs374527572 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632076 | GCCTGGGTGACAGAG[C/T]GAAGACTCCATCTCA | 7088 |
rs374551075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645424 | TAAAATAACTAAAAG[C/T]GTGTCATTAGATTGT | 7088 |
rs374554612 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595981 | ACCACAAATCAAGCT[A/G]GGCGCCTCCAGGTAA | 7088 |
rs374562149 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597844 | CACCGGGCTCCTTCG[A/C]AGCTGTGGTGAACTG | 7088 |
rs374569361 | snp | C/G | 1.64768e-05 | 0.00287021 | missense | TLE1 | GRCh38.p7 | 9:81613439 | GGACGGAGGCCTGGA[C/G]TGGCGCTGGTGCCCG | 7088 |
rs374573731 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683031 | AACCACAATTATACC[A/G]TTCTTGATTTGGATG | 7088 |
rs374579865 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615846 | ACAAAGAACAGAAGG[A/G]TGAGTTTCACTATTA | 7088 |
rs374614888 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585211 | TCTTCAATAAATTCC[C/T]GCCCACCCCTCTTCA | 7088 |
rs374667036 | in-del | -/TTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616588 | TTCACTGTTAGTTTT[-/TTTT]CATAACATTATTCAA | 7088 |
rs374675246 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607060 | GAGACCCAGTGTCTC[A/T]AAAAAAAAAAAAAAA | 7088 |
rs374682917 | in-del | -/TCATCCCGCC/TCATCCCGCCTGTA | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587926 | GTGTGTGTGTGTGTG[-/TCATCCCGCC/TCATCCCGCCTGTA]TGTGTGTGTGTGTGT | 7088 |
rs374695233 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657771 | ATAACCTATGCACAT[C/T]TACCCATACACTTTA | 7088 |
rs374714602 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598051 | AGACCCCAGAGAGGA[C/T]GGCTGTGGTCAAGCC | 7088 |
rs374750987 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636178 | CATTTGAGATCATAA[C/T]AACAATTTCTTTATG | 7088 |
rs374819476 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639863 | TGCTGGGATTACAAC[A/G]GGCATGAACCACCGC | 7088 |
rs374832161 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604710 | CTAAAGGGACATTAA[A/G]GTCCCTCCTGCCCCA | 7088 |
rs374852829 | snp | A/G | 1.65119e-05 | 0.00287327 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685800 | TTGCTAATATCATAT[A/G]AAAAAGGAAAAAGTC | 7088 |
rs374885769 | in-del | -/ATAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675334 | GTAAAGACTAAGTAA[-/ATAA]TCAGTGGTTATACTC | 7088 |
rs374897058 | snp | C/T | 0.000272746 | 0.0116747 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688268 | GGCCGGGGCTCTGTT[C/T]CCCGGCAACTCAATT | 7088 |
rs374897124 | snp | A/G | 3.29636e-05 | 0.00405964 | utr-variant-3-prime | TLE1 | GRCh38.p7 | 9:81584170 | TTTTGGCCCAATTCA[A/G]CTATAAACGTTAAAC | 7088 |
rs374938462 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680891 | TAGGGGGAAAAAAAA[C/T]CTCAAAGTGAGAAAC | 7088 |
rs374938679 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626408 | CAAGCCATCACCCTG[C/T]GCTGCACTTTTTGCT | 7088 |
rs374940230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680329 | CAAAGGCAGAAAGAG[C/G]GGGAGGCAAGGGAGG | 7088 |
rs374977974 | snp | C/T | 5.89478e-05 | 0.00542867 | intron-variant | TLE1 | GRCh38.p7 | 9:81593290 | CTTTTGGAAAAACGA[C/T]TGGAGAGAAGACAGA | 7088 |
rs375002324 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609321 | AACCCCCGACCTCAG[G/T]TGATCCACCCGCCTC | 7088 |
rs375003599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81631492 | CTTTCTCCAGTCTTG[C/T]TTCTTTTAGTAATTG | 7088 |
rs375021568 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665891 | AAAGAATTCAGTTGC[A/G]TTTTCCAAGATGAAG | 7088 |
rs375032710 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592320 | CCGAGATCCGGCCAC[C/T]GCACTCCAGCCTGGG | 7088 |
rs375045790 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81667722 | GTATTCCTGCTCCCC[C/G]CCAAGCTGAGTGGCT | 7088 |
rs375045955 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644918 | AGAATCGTTTGAACC[C/G]GGGAAGCGGAGGTTG | 7088 |
rs375098749 | snp | A/T | 0.000169448 | 0.00920302 | intron-variant | TLE1 | GRCh38.p7 | 9:81634345 | AGGAGGAGGAGGAGG[A/T]GGTAGTGGTGACAGT | 7088 |
rs375103420 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81682148 | AATCCCAGCTACTCC[A/G]GAGGCTGAGGCAGGA | 7088 |
rs375105369 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681234 | CAGATTTTCAGAGCT[A/G]GTCTTTTCATTTATT | 7088 |
rs375135930 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81608151 | TGGTGGCTCATGCCT[A/G]TAATCCAAGCACTTT | 7088 |
rs375158435 | in-del | -/CTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627145 | TTACATTTATACCTC[-/CTT]ATCTCAAAGATGAGG | 7088 |
rs375169580 | snp | A/T | 7.68433e-05 | 0.00619804 | missense, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687355 | TACTGCGCCTGCAGG[A/T]ACTGGAATTCCTCTT | 7088 |
rs375226687 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618045 | CAACAACAACAACAA[A/C]AAATTCAATGATGCG | 7088 |
rs375249960 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623657 | ATTAGCCGGGTGGTG[A/G]TAGACACCTGTAATC | 7088 |
rs375322447 | in-del | -/AAG | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81683911 | TCTCCCTACATGATA[-/AAG]AAGAGGTCATCCCGC | 7088 |
rs375328007 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603769 | CACTTTGGGAGGCCA[A/T]GGTGGGTGGATCACC | 7088 |
rs375332783 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629768 | AATGTAAGTATTTGT[A/G]TATCTAAACACACCT | 7088 |
rs375339918 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594597 | CACTACTTCCACTTT[C/T]TTAACTTGAAATCAC | 7088 |
rs375357643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81595775 | GGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 7088 |
rs375358720 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682489 | AGCCACCAATGACAA[C/T]TTATAGCATGGCTTC | 7088 |
rs375370302 | snp | A/G | 0.000307953 | 0.0124049 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585533 | TTTCAGGGACAGCAC[A/G]CAGCTCTCATGCAGG | 7088 |
rs375436322 | snp | A/C | 3.30109e-05 | 0.00406256 | intron-variant | TLE1 | GRCh38.p7 | 9:81584415 | GCGACACTGTGGTCA[A/C]ACTGTGGATCTAGGT | 7088 |
rs375445717 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664025 | CTTCACAGGCAGAAA[G/T]AATGATGCATCAACC | 7088 |
rs375446667 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670104 | TGGATATCTTATCTT[C/T]CTATTGCTCTCAAAT | 7088 |
rs375457973 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648509 | ATCAACTGAAAAAAA[-/A]CAAATATATGTGTGT | 7088 |
rs375458372 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636546 | GAGAGGCTAAGCAGA[A/G]GGGAAGGAATCTAAC | 7088 |
rs375461359 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607171 | AAAGTACCCCGACAT[A/G]GTATCACAACATTGG | 7088 |
rs375533201 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679366 | ACAAGCAGCAAATCT[C/G]AAATCATTCCTTTGC | 7088 |
rs375550899 | snp | A/G/T | 0.000362474 | 0.0134575 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590882 | GCAGACCTTGGAATC[A/G/T]GGGCTGATGGCCAGG | 7088 |
rs375571812 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81685694 | TTTGTGCATTTCAAT[A/G]TTTAATCCATATGAC | 7088 |
rs375599212 | snp | A/G | 0.000115734 | 0.00760616 | synonymous-codon, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587822 | GTCTGTGTGGCCCTG[A/G]AATTGCCTGATAAAA | 7088 |
rs375709041 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81652224 | CGTACCCCGATGATG[A/G]CATTCAATTCTGCCA | 7088 |
rs375716909 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81591833 | TTTTTTAAAAAATGC[A/T]CTAATAACTACTCTA | 7088 |
rs375787553 | snp | A/C/T | 0.00626593 | 0.0556218 | intron-variant | TLE1 | GRCh38.p7 | 9:81584568 | TCACAAGGTTAAAAT[A/C/T]CCTACTATACAATTA | 7088 |
rs375805335 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585307 | GCAATCACATTGCCT[A/G]CTGACTTTTCTCAAA | 7088 |
rs375842115 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613758 | CACACTTCTTCCTCC[A/G]CAGATTTTATTTTAA | 7088 |
rs375857314 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683196 | AGCATTAAAGCTCTC[A/T]GTACGGAAAGTTTCC | 7088 |
rs375908856 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684109 | TCTTACTCTTCCATA[A/G]TATCTGTTATCCAAA | 7088 |
rs375954684 | snp | C/T | 2.70384e-05 | 0.00367674 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634117 | TGGTGCTCTGCATCG[C/T]GGTGCTTCTTGTCAT | 7088 |
rs376037246 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585006 | CATCCATCCATCTAT[C/G]CATACTGTGAACAGA | 7088 |
rs376059183 | snp | C/T | 1.64988e-05 | 0.00287213 | intron-variant | TLE1 | GRCh38.p7 | 9:81616630 | GAAGACAAACTTTGA[C/T]GAAAAGAATGGTTAC | 7088 |
rs376094211 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677322 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGTG | 7088 |
rs376118714 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632473 | TTAAATGTTCAGTAT[C/T]CCTTTTTTTTTTTTT | 7088 |
rs376146312 | snp | A/C/G | 0.000362735 | 0.0134629 | intron-variant | TLE1 | GRCh38.p7 | 9:81633373 | TCTCTGTCTGCTCCC[A/C/G]AGGTTACCAAGAAAC | 7088 |
rs376167085 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634205 | CACTGCCCCCGAGGG[A/G]CGGGATTCCAGGAGG | 7088 |
rs376193182 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585894 | TAAGAAATGATTCCT[A/G]ATAATAATGGCATTC | 7088 |
rs376219292 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653471 | GACTTTGTAACTAAA[A/C/T]AAAATAGCTTATACA | 7088 |
rs376224094 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595277 | GAACAGGAACCTATG[C/T]CACTTATTATGGGAT | 7088 |
rs376232181 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81682371 | AACACGTGCACACAG[C/T]TGTAGGCAGAGCAAA | 7088 |
rs376235867 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676008 | CAGGCCGACCCACAC[C/T]AGTTTTCTTGATTCG | 7088 |
rs376244481 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640794 | CACAGTCACAGCACA[C/T]GGCTTATCACCATGT | 7088 |
rs376247630 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81593731 | TAGATATATTTCAAC[-/A]GCAAAAACAACCTCC | 7088 |
rs376255629 | snp | C/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690093 | GAGGGCTCGAGTTAG[C/G]AAAAATCCTGCCACT | 7088 |
rs376266114 | snp | C/G/T | 5.00115e-05 | 0.00500037 | intron-variant | TLE1 | GRCh38.p7 | 9:81613335 | AAATCAAGCTGGGAA[C/G/T]GGGAGAAACCAAACA | 7088 |
rs376267304 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81656016 | CAACCCAATTCTCCC[C/T]GACCACCAATGAGAC | 7088 |
rs376297505 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670714 | CCAGAAGCTAATCAG[-/A]AAAAAAAAAAATTAA | 7088 |
rs376330585 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666145 | TCACAGGAAATGGTA[C/T]TGACTTGTCCCAGGA | 7088 |
rs376338862 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688701 | CGCCTCCTCTTCGGG[C/T]TTTCCCCGAGGCGGC | 7088 |
rs376377585 | in-del | -/GCACTGA | | | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590171 | ACAGCTCTGGTGTGA[-/GCACTGA]CTTCTGAAGGGAGCA | 7088 |
rs376383387 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688020 | GTCAAGTAGGAAGGA[A/C/G]CCCAAAGGGAGGGAG | 7088 |
rs376401732 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81651014 | TCCTTGGCTCTTATG[-/T]TTTTTTCTCCATCTC | 7088 |
rs376436204 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681531 | CTCCAGCCTGGGTGA[C/T]GGAACGAGATTCCGT | 7088 |
rs376454144 | snp | C/T | 3.2975e-05 | 0.00406035 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81613416 | TGGCTGGAGGCTTGC[C/T]GAGACCTGGACGGAG | 7088 |
rs376527739 | snp | G/T | 8.26788e-05 | 0.00642904 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687311 | CGCCCGCGACCACTC[G/T]CATGGCGCGGCCGGA | 7088 |
rs376546838 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638205 | CCATCTCCTGTCCCC[C/G]CTTCTCAATGCCTGT | 7088 |
rs376575728 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638917 | AGCGTGCGCCACCAC[A/C]CCAGCCGATACATGC | 7088 |
rs376585098 | snp | A/G | 0.000481004 | 0.0155007 | intron-variant | TLE1 | GRCh38.p7 | 9:81620576 | CAAGACAAAAAAATT[A/G]ATCAAAGATTTCTTC | 7088 |
rs376588131 | snp | C/T | | | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583593 | CAATTCAAAACTTCC[C/T]CTACAAATGTATAAT | 7088 |
rs376593345 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688311 | TCCAACTTTAATCCC[A/G]CCGAGGAAAATTAAG | 7088 |
rs376610282 | snp | A/G | | | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583240 | AAAAAAAAAAAAAAA[A/G]GGAGAGAGAGAGAGA | 7088 |
rs376728327 | snp | A/C | | | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583219 | ACTCAAATCTTTAAA[A/C]AAAAAAAAAAAAAAA | 7088 |
rs376775851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687557 | GTGGCTGAAAACGAG[A/G]CCCCAAACTCGAGTT | 7088 |
rs376779352 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648724 | ATCAATTATCCCTGC[A/G]TTCAGGCAGCCATTA | 7088 |
rs376814117 | snp | A/G | 0.000167311 | 0.0091448 | intron-variant | TLE1 | GRCh38.p7 | 9:81633334 | GTGTGTGCAGCAGGC[A/G]TTTGAGTACTTACTG | 7088 |
rs376817505 | in-del | A/TAAC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618027 | CAAGACTCCGTCTCA[A/TAAC]AACAACAACAACAAC | 7088 |
rs376844498 | snp | C/T | 2.61599e-05 | 0.00361652 | missense | TLE1 | GRCh38.p7 | 9:81611779 | CCTACCATGGGGGAG[C/T]GCCCGTAGGCCACCA | 7088 |
rs376870709 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623473 | GAGGTTGCTTTGCAT[G/T]AAGCTATTTGAAAAT | 7088 |
rs376892081 | snp | C/T | 0.000135881 | 0.00824149 | intron-variant | TLE1 | GRCh38.p7 | 9:81585688 | GGCTCACTCATTATT[C/T]CGCCTGATACACTTA | 7088 |
rs376900752 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689853 | CCTCCTCCGCCAGCC[A/G]CGTCCTCCCGGGCTT | 7088 |
rs376952071 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616045 | CGTGGAAGCTGGACT[A/G]CTAGAAGCATCCTTC | 7088 |
rs376966361 | snp | A/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588968 | ACTGCCCTAAATTCT[A/T]AGCCAAGACGTGAAC | 7088 |
rs376990174 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636903 | AACTACTGGGGAGGC[C/T]GAGGCAGGAGAATCA | 7088 |
rs377082421 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689478 | ACCCGCCGCTGTTTC[C/T]GCTGCTGCTGCTTCT | 7088 |
rs377083985 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677952 | TGAAAAAGTTAATTC[A/G]ACGGATAGAATTTTC | 7088 |
rs377090742 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685776 | GTTTTTTACACTCTG[C/T]TAACACGTTTGCTAA | 7088 |
rs377144163 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632736 | CGCACACAGCCCTGT[C/T]CACTGAATTTCCTTC | 7088 |
rs377146765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610865 | GCTTAAGGATTCATA[C/T]ATGGATTCCCTACTT | 7088 |
rs377152054 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598732 | GCAGTTTCCTAAGGG[G/T]GAAAGGCAGTCTCTA | 7088 |
rs377175662 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-3-prime | TLE1 | GRCh38.p7 | 9:81584149 | TATTTCTATAAATTC[A/G]AAACATTTTGGCCCA | 7088 |
rs377219280 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586163 | GCTGGGACTACAGGC[A/G]CCCACCACCACGCCC | 7088 |
rs377230786 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654584 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 7088 |
rs377232053 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81639479 | CTAGGCATTAGTTTA[A/C/T]AGTAATTAGGAAATT | 7088 |
rs377236146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81621942 | AAAAGCAGCTGGGAG[A/G]GACCAACGCAATTCA | 7088 |
rs377239895 | snp | A/C | 1.77998e-05 | 0.00298321 | intron-variant | TLE1 | GRCh38.p7 | 9:81591099 | GAATTACCGAGCAAT[A/C]ATAGCACCATGTTCT | 7088 |
rs377245680 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614115 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTCG | 7088 |
rs377245920 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595843 | AAAAAATTAAAAAAT[A/T]AAAGTAAAACAATTG | 7088 |
rs377274586 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663618 | GGTATCCGCACAGAA[C/T]AGACTTTTTTTTTTT | 7088 |
rs377289315 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650187 | CATTTGCCCTTCTAA[A/C]AAGATCTGCTATTTT | 7088 |
rs377294233 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636636 | ATCTAGAATGGAGTC[A/T]CCAGAAGATGACTTC | 7088 |
rs377306593 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688119 | CGCTGAGGGCGAGAA[A/G]GTCCGCCGGGCCTCA | 7088 |
rs377307588 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670352 | TTTTTTTGAGACAGA[A/G]TCTGGGTCTGTCGCC | 7088 |
rs377313793 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | TLE1 | GRCh38.p7 | 9:81653912 | TAACATCTTAAAACT[A/G]GCTAATTTGCAAACA | 7088 |
rs377346839 | snp | A/G | 0.000222717 | 0.0105503 | intron-variant | TLE1 | GRCh38.p7 | 9:81610323 | AATAAGGCATTGCAG[A/G]CTCAGTTTATTGCAG | 7088 |
rs377366587 | snp | G/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686178 | GATTCCTCCTCATGG[G/T]CATCTGCTCCCTACC | 7088 |
rs377398874 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610445 | TCTTTTTAATTACTA[C/T]GCAAGAGGTAATATA | 7088 |
rs377409221 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | TLE1 | GRCh38.p7 | 9:81584145 | TTTCTATTTCTATAA[A/G]TTCGAAACATTTTGG | 7088 |
rs377467983 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669503 | GTCTGCAAGCAGTAC[C/T]GTAAAGTAGAAATTT | 7088 |
rs377542226 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | TLE1 | GRCh38.p7 | 9:81652177 | AATGAAAGCTGGTTA[C/T]ACACACTGTAGGAGG | 7088 |
rs377547480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590289 | CAGGCAGAGCCCTGC[A/G]GGCTCCTGGGTGGAA | 7088 |
rs377563316 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624103 | CCCAAAAACTTACTT[A/G]AAATCCACCCTGGCT | 7088 |
rs377565312 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644521 | AATAGGCAAATTCAT[A/T]GAGATGGATAAGCAC | 7088 |
rs377589718 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639588 | TTGTTTTTTTTTTTT[-/G]TTTTTTTTTTTTTTG | 7088 |
rs377648854 | snp | A/G | 3.69174e-05 | 0.0042962 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611814 | GGCCGCGGCGGCTGC[A/G]GCGCTCATCTGGGGC | 7088 |
rs377654687 | in-del | -/CATG | 0.00795532 | 0.062565 | intron-variant | TLE1 | GRCh38.p7 | 9:81681751 | GTAGTTTTATCTACC[-/CATG]CATGGCCTGTGACCC | 7088 |
rs377660324 | in-del | -/T | 0.469049 | 0.120489 | intron-variant | TLE1 | GRCh38.p7 | 9:81623616 | AAACCCCATCTGTAC[-/T]TAAAAAAAAAAAAAA | 7088 |
rs377672251 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81635631 | CAGATTCTGATTTGT[A/G]CTCACTTCCTTGGGA | 7088 |
rs377713712 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627996 | GACCAAGGTGGGAGA[A/G]TCACTTGAAGCCAGG | 7088 |
rs377715789 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611090 | AGCCAAGAGAAATGA[C/T]GGTGGGACTTTATAC | 7088 |
rs386361340 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625912 | ACCTCAGAAACTACT[-/AA]AAAAAAAAAAAAAAA | 7088 |
rs386415266 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625932 | AAAAAAAAAAAAAAA[-/AA]GCAACTTTAATAAAA | 7088 |
rs386415267 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629177 | TTGTCAAATGACTCA[-/A]AAGTATTTAAAAGCA | 7088 |
rs386415268 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629179 | GTCAAATGACTCAAA[-/A]GTATTTAAAAGCATG | 7088 |
rs386415270 | in-del | -/GAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641237 | ATAAAAATAAAGAAG[-/GAA]AAAACTGGTATGCTA | 7088 |
rs386735588 | in-del | AC/GAACGAAA | | | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583258 | AGAGAGAGAGAGAGA[AC/GAACGAAA]GAAAGAAAGAGAGAA | 7088 |
rs386735589 | multinucleotide-polymorphism | CC/GA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597299 | AAAAAGCCAAGTGAA[CC/GA]TACGTTGAATTGAGG | 7088 |
rs386735590 | multinucleotide-polymorphism | AG/TA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623067 | CAAACAGTTCCAGCC[AG/TA]ATGAGCTTCGCTGGC | 7088 |
rs386735591 | multinucleotide-polymorphism | GCA/TCG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649347 | CCTCTCTCTGTCTCC[GCA/TCG]AAGAGCACCCACAGG | 7088 |
rs397692663 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648846 | CTTATGGTGTAAAAA[-/A]CGATCCTGATCTAAA | 7088 |
rs397697817 | in-del | -/GAAAGAAAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642727 | AGAAAGGAAAGAAAG[-/GAAAGAAAG]AAAGAAAGAGAGAGA | 7088 |
rs397703983 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651979 | ATTAATAGATTTTTT[-/T]GTCCCCTCCTAAAAT | 7088 |
rs397709246 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672477 | ATTTTTTTTTTTTTT[-/T]GCTTCCCCAAATATT | 7088 |
rs397743781 | in-del | -/TA | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81632137 | AATGGCAAAACAATA[-/TA]AGGCTTCCTCCATAA | 7088 |
rs397745844 | in-del | -/CA | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81607356 | ACACACACACACACA[-/CA]TATAAGGAATAGGGT | 7088 |
rs397750535 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665875 | CATTTTTTTTTTTTT[-/T]AAAGAATTCAGTTGC | 7088 |
rs397810371 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627330 | CACTTTTTTTTTTTT[-/T]AAGAGTAAAGATGCC | 7088 |
rs397820258 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684256 | ATTTACTATCAAGAA[-/A]GTTACAAGTGCCTGA | 7088 |
rs397893862 | in-del | -/A | 0.499809 | 0.00978247 | intron-variant | TLE1 | GRCh38.p7 | 9:81667386 | GAGACAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 7088 |
rs397951247 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664720 | TAAGAAAAAAAAAAA[-/A]TAAGTGAGGTACCTT | 7088 |
rs397969490 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645379 | CCAAAAAAAAAAAAA[-/A]TAATAGTAATAATAA | 7088 |
rs398011200 | in-del | -/A | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81594359 | GCAGCCATAAAAAAA[-/A]GGATGAGTTCATGTC | 7088 |
rs398011201 | in-del | -/A | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81600645 | AAAAAAAAAAAAAAA[-/A]CCTACCCAAATATCA | 7088 |
rs398068722 | in-del | -/CA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625595 | ACAATTATGAAACCA[-/CA]TACCTTCATGTAAGA | 7088 |
rs398068723 | in-del | -/TT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627329 | CTCACTTTTTTTTTT[-/TT]AAGAGTAAAGATGCC | 7088 |
rs398068724 | in-del | -/AAAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681559 | CGTCGCGCAAAAAAA[-/AAAAA]GAAAAAAAATTCTTC | 7088 |
rs398087384 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634483 | GAGGAAAGGGGAAAA[-/A]ATGCGATTAGTGCTT | 7088 |
rs398087385 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668180 | CTCGAAAAAAAAAAA[-/A]AGAAGGATATGTAAA | 7088 |
rs527247315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611214 | AAGAGGCAGGGCAAA[C/G]AGACGAGAGACAGCC | 7088 |
rs527260521 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654485 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACTCC | 7088 |
rs527261784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81654993 | AGTAACAAACTCAAA[G/T]ACCTCACCGACAGGG | 7088 |
rs527306196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655224 | CAAAAATTAGCCGGG[C/T]GTGATGGTGGGCGCC | 7088 |
rs527325928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617454 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 7088 |
rs527351150 | in-del | -/AGG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652300 | GATGCTTTGAAAACA[-/AGG]AGAAGAAAGGGCATT | 7088 |
rs527363169 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81622857 | TGGAAAGGCCCAGAA[A/C]CACCACACTCAGACC | 7088 |
rs527414110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616774 | TTAGATTTCTTTCTA[C/T]AGTTCCTGGTAGCAG | 7088 |
rs527452209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81666172 | AGGATGGAAAAAGGA[C/T]AGCTTTTGGTGGGCT | 7088 |
rs527494482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587409 | ACATTCTTCAATGTA[C/T]AAATCCCTTAAACAA | 7088 |
rs527625951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592152 | TCACAAGGTCAGGAG[A/T]TCGAGACCATTCTGG | 7088 |
rs527635403 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596213 | TGCACAGGAGGCCTG[C/T]GATCATCATATGGAG | 7088 |
rs527640562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668607 | CCTCCAAGATAACAA[C/T]CAACCTACTTTCAGG | 7088 |
rs527692198 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683932 | AGGTCATCCCGCCAC[A/G]TAACCTACAGGAACC | 7088 |
rs527693612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661773 | CCCCCCCCAAAAAAA[A/T]TGTACACAGAAACCT | 7088 |
rs527726431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624435 | ATCATCCTACAGACC[C/T]ATTTGCCACTGCAGA | 7088 |
rs527765939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674262 | TGGCTTGCCTTCTAA[C/T]GCAGTTTTCTATTGT | 7088 |
rs527775378 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625061 | ATCAGAAACATAAAG[A/G]GGGTCCAAAAATGGG | 7088 |
rs527778448 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591754 | GATACTCCTACTGCT[A/G]TAGAATATTGGGCCA | 7088 |
rs527787181 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81631391 | ACCTCTGCCTATTCA[C/T]ACCCCTGGCATTTCA | 7088 |
rs527818446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588072 | GAAATGGAATGCCAC[C/T]GCAGGTCACTACCCA | 7088 |
rs527819028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81593829 | GAAAATAAGAGATTA[A/T]CTTATATGGCTGTAA | 7088 |
rs527839209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81598787 | AGATAATGAAAGCAA[C/T]GACAATAATGAAGTG | 7088 |
rs527854069 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686111 | ACCATTCTTCTTGGT[A/G]CCTATCTGGTTAGAT | 7088 |
rs527911380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81637213 | AAATATACAAATTAG[A/C]CGGGCGTGGTGGTGC | 7088 |
rs527950399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81649041 | GAAAAGAATTGGTAA[A/G]AAGCAACAGTCAAAA | 7088 |
rs527967913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611627 | TGTGTGGCTGGGAGA[C/T]TGGGCGTCTTTGTCT | 7088 |
rs527968820 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689542 | GCCTCTCGCGCCGCT[C/T]ACATTAACACGCGGT | 7088 |
rs527970876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604766 | CAGGAGGCACTCATC[C/G]ACCTGCACATGGATC | 7088 |
rs527999721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81605307 | GAGTGCAGTCATCGA[A/G]AGTGAGCGACAGCAA | 7088 |
rs528006703 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81610617 | TTAGGATTTCTCAAC[A/C/T]TCAGCACTATTGACA | 7088 |
rs528041775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671620 | ACTACACTCCAACCT[A/G]GGCGACAGAGTGAGA | 7088 |
rs528093639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664863 | TCCTGTTGGAGTCTA[A/G]GCCTGAGAATATTCG | 7088 |
rs528127303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81640633 | CACAAGGAATAAAGC[A/G]ATCTCATCCATGTCA | 7088 |
rs528132924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615585 | GGGCATGGTCGCGCG[C/T]GCCTGTAATCCCAGC | 7088 |
rs528151140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682655 | CCACCACACACACTA[A/G]GCACAGCTAGGCAAA | 7088 |
rs528162670 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81593919 | ATTATATAAAACAGC[A/C]AAGTGTGCAGCTAAA | 7088 |
rs528172243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602368 | AGTGTTTCTGATGTC[C/G]GATTTTTTTCAGACT | 7088 |
rs528174617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676789 | GGAGTTCCCAGGGTG[A/C]GGCCAGGTTTGACAT | 7088 |
rs528183283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596041 | CAATCTCAGATTTTT[C/T]AGAGAAAGGAGATTT | 7088 |
rs528232813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81590157 | AAGACTTTTTGAGAA[C/G]AGCTCTGGTGTGAGC | 7088 |
rs528253869 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637038 | AGAAAAAAAAAGATT[A/T]CCCCTCCCATAAATC | 7088 |
rs528263987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682161 | CCGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 7088 |
rs528286084 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81645769 | TAAAATAAAATAAAA[C/T]AAAAATAAATGCTTG | 7088 |
rs528291065 | in-del | -/CATT | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81640288 | AAAAATACTATTCAA[-/CATT]CAATCACATTCACTG | 7088 |
rs528322883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639874 | CAACAGGCATGAACC[A/G]CCGCGCCCAGCTGAG | 7088 |
rs528353177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81607741 | GGCTGGAAGCAGGGG[A/G]GCATTCCCAAATTCC | 7088 |
rs528354851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613954 | ACTCTGTCACCCAAG[C/G]TGGAGTGCAGTGGCG | 7088 |
rs528355889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652015 | TCCTGTCATCTTCCT[C/T]ATGCTAAGCCCTCTT | 7088 |
rs528357492 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81658101 | ATTTTTAGTAAAGAC[A/G]GGGTTTCACCATGTA | 7088 |
rs528391669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81608524 | GTTTCTAAAAATAAA[A/T]AACTCACTAATGTGA | 7088 |
rs528428454 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81630585 | CTTCAGGGCCCTCAA[C/T]AATTTGATTTCAAGG | 7088 |
rs528443460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683954 | ACAGGAACCCAGAAG[A/G]ATTACACACCTCTTT | 7088 |
rs528444992 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81597081 | GCTACGTCAACTGCG[G/T]TCTTGCCAATCAGCC | 7088 |
rs528450790 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81604124 | TAATAAGACTTGCAT[C/G]CATTTCTCCTGTTAA | 7088 |
rs528461541 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643102 | AGCAATTGGTCAAAG[A/G]GTACAAGGTTTCAGT | 7088 |
rs528465751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647692 | TGGGAAGGTAGACGG[C/T]ATTACCATCTACAGA | 7088 |
rs528509440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81642101 | AGACAAAGATAGTGT[C/T]AGTGATGGTGTGGAG | 7088 |
rs528547238 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81647134 | ACTGCTCAAATTTTC[C/T]TGCACCCAACTGTCA | 7088 |
rs528578749 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688376 | CCACGCACGCGCGCT[C/T]CGCCGGGCGCACCGG | 7088 |
rs528579180 | snp | A/C/T | 8.50455e-05 | 0.00652047 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688245 | TGCGGGAACATCGCT[A/C/T]TGGCGGCGGCCGGGG | 7088 |
rs528589674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683476 | AAAAAGCATCAATTT[C/G]AGCTTGGCTACACCC | 7088 |
rs528599855 | in-del | -/TCAG | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81596321 | ATGGATGTTAATACA[-/TCAG]TCAGTCACAGGGGGC | 7088 |
rs528652125 | in-del | -/AG | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81617775 | CAAGCCTATAATCCC[-/AG]AGCACTTTGGGAGGC | 7088 |
rs528657038 | snp | C/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687853 | GGGCCACCTCCAGAC[C/G]CACCGGAACCGGGGC | 7088 |
rs528724877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615296 | ATCACGCCACTGCAC[G/T]CCAGCCTGGGCAACA | 7088 |
rs528727789 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81628279 | TACTATCACCATTTA[C/T]AGATGGGACTAGGAA | 7088 |
rs528807407 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81658928 | TATTTATTTTTTTTT[C/T]AGATGGAGTCTTGCT | 7088 |
rs528844706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686734 | GTAAGTCTCATTACT[C/T]GAAGAAACTAAGGCT | 7088 |
rs528845413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599670 | TCAATTTTTTTTAAG[A/G]GTCTGCACATCTAAC | 7088 |
rs528855108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81606808 | ATATATATATAGAGA[A/G]AGAGGCAGTAAGATT | 7088 |
rs528861719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644280 | GTACACAAATGTTCA[C/T]AGCAGCATTATTCAA | 7088 |
rs528863751 | in-del | -/TTAAT | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81675124 | AAATTCCCCATATTA[-/TTAAT]TTATTTCTTGATTTT | 7088 |
rs528897256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644717 | AGACGAATTTGGCCA[C/G]GTGCAGTGACTCATG | 7088 |
rs528974046 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | TLE1 | GRCh38.p7 | 9:81606015 | GCCAACAGACACATG[-/A]AAAAATGCTCATCAT | 7088 |
rs528992390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656276 | GCAAGGCTTTCCTTT[C/G]CAACAGGGTTCTGCA | 7088 |
rs529008542 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597841 | CCCCACCGGGCTCCT[G/T]CGCAGCTGTGGTGAA | 7088 |
rs529020536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81606128 | AGGAGACAACAGATG[A/C]TGGAGAGGATGTGGA | 7088 |
rs529033680 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81635361 | CCCCGTTCCCAAATG[C/G]CTTTTCCATGACTGC | 7088 |
rs529054778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655859 | CCCTGTCTCAAAAAA[A/G]AAAAAAAAAAGAAAA | 7088 |
rs529163299 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623595 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 7088 |
rs529199479 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654621 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 7088 |
rs529199772 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81661127 | GACTCGGTCTCAAAA[A/T]TAAAAATAAATAAAA | 7088 |
rs529225334 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599547 | AAAACTAATAAAGGC[A/G]GTGGCTGGGAGGAAT | 7088 |
rs529237108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668431 | TAGATGACAGGTGCC[A/G]TGGTGTATGGATTCA | 7088 |
rs529245774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588455 | GGTCACGCATGCCGG[C/T]CTCCTGACCTCAGAG | 7088 |
rs529259024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81663700 | CAATCTCGGCTCACT[A/G]CAAGCTCTGCCTCCC | 7088 |
rs529327501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651348 | CCTGCAGTGGGGGGC[A/G]GAGGATGAACTCATG | 7088 |
rs529329420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657807 | TCTCCAGATTACTTA[A/G]AATACCTAATACAAT | 7088 |
rs529368052 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607043 | AGCCTAGGCAACCCA[A/G]GGAGACCCAGTGTCT | 7088 |
rs529394238 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584074 | CTCAAAGTAGTTTTC[C/T]GTCAAGGTTTGGAAA | 7088 |
rs529396656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675962 | CCTCAGCCTCCCAAA[A/G]TGCTGGGATTACGGG | 7088 |
rs529419262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669464 | TTTTAGATCATCAGC[C/T]GAAGTCTGGAACGCA | 7088 |
rs529434048 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627318 | AAATTGTTCTCTCAC[-/T]TTTTTTTTTTTTAAG | 7088 |
rs529438734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81663092 | CTCAAATTATCCACA[C/T]GCCTCGGCCCCCCAA | 7088 |
rs529452345 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583629 | CTTATAAAACCCACA[C/T]TGATGATCCCAAAGC | 7088 |
rs529501614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81631931 | AACATGGAGAAACCC[C/T]GTCTGTACTAAAAAT | 7088 |
rs529503626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81639150 | AGGCTGGTCTGGAAC[C/T]CCTGTTTTCAAGCAA | 7088 |
rs529561536 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674608 | CTAACAATATTTCCC[C/T]CAGCAAATATACTGG | 7088 |
rs529583447 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81681480 | GCTTGAACCTGGGAG[A/G]CGGAGGTTGCAGTGA | 7088 |
rs529583577 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81675489 | AATTCACACCAAACC[C/T]AGGCCCCAGCAACAT | 7088 |
rs529653429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81666757 | TCCAGCCTGGGTGAC[A/G]GAGCAAGACTCGTCT | 7088 |
rs529676572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659909 | GAGAGATCTTCCCAA[A/T]CCCTCAAGGCCTGCC | 7088 |
rs529689623 | snp | C/T | 0.000164829 | 0.00907674 | missense | TLE1 | GRCh38.p7 | 9:81616094 | TCGATTCCATTTTCC[C/T]GGGGCGAGTGGGCAG | 7088 |
rs529761580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621889 | GGGCTCTTTTATTCA[C/T]GACTGTTCAAGCTAC | 7088 |
rs529764351 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81610742 | AGGAATCCATACCTG[-/C]CCCCCCCTCCCACCC | 7088 |
rs529768053 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655794 | CAAAGTCGAGCCTGC[A/G]GTGAGCTGAGATCGC | 7088 |
rs529801384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665370 | AATTACTGGCAGATA[A/G]TAACTTTTATGTTCC | 7088 |
rs529830730 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677836 | TTAGTACACTGGGAA[C/T]AGATTTCAGGGATGA | 7088 |
rs529848598 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81680933 | ACACACAGGGTTAAA[A/T]AAAAAAAACAAAAAA | 7088 |
rs529862740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597358 | GTGGGTCAGGGAATG[A/C]GGAAAGGGAGGAAGA | 7088 |
rs529873210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672492 | TGCTTCCCCAAATAT[G/T]AGTACATCAGCAGCA | 7088 |
rs529902607 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81641984 | CGGAGATCGCGCCAT[C/T]GCACTCCAGCCTGGG | 7088 |
rs529904175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634695 | GGGATGAGATCCAGC[A/G]TGTCACTCAATCTAA | 7088 |
rs529926391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628408 | CCATGGTTCCCATAG[G/T]CCTCCGGGAATGAAC | 7088 |
rs529935599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603355 | GTTCAGGATATGCCA[A/C]ACCAAATATGCCCTT | 7088 |
rs529936063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596651 | GAATATCGCTCACAC[C/G]TGAATTCAGAATGAA | 7088 |
rs529936100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683397 | CCTGTCAAATCTAAT[A/G]AGAGCTCCAAAGGCC | 7088 |
rs529939311 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81635317 | TGAGGAAAGCACTTA[A/T]GTGTGGGACTCCAGC | 7088 |
rs529948556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683933 | GGTCATCCCGCCACA[A/T]AACCTACAGGAACCC | 7088 |
rs529967055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81641579 | ACTCAATAGTACAAA[A/G]ATTAAAAAATAAGTA | 7088 |
rs529995219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674109 | TCCCCAGCCATCAAC[C/T]AGATGTTCCCACACA | 7088 |
rs530013218 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81677739 | GTAGTTTGACAAACT[A/G]CAAGATTTGGACGCG | 7088 |
rs530032373 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600630 | GCATTTAATAGACCA[-/A]AAAAAAAAAAAAAAA | 7088 |
rs530053643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81667890 | TACTCAGACCCGGGC[A/G]TGATGGCTCACACCT | 7088 |
rs530067128 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646685 | AAACCAATCATCTCA[C/T]GCAAGAGTGGAGAGC | 7088 |
rs530072232 | in-del | -/A | 0.469148 | 0.120308 | intron-variant | TLE1 | GRCh38.p7 | 9:81615545 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAA | 7088 |
rs530091489 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81636458 | TCTGGGTGGGGGGTG[A/G]GGGGAATGCAATGAT | 7088 |
rs530135673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597807 | CACAGCAGAGGTGAA[G/T]GAACTAAAAGCAAAG | 7088 |
rs530158966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643339 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 7088 |
rs530195668 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81679053 | TTCCAGAGGCTGAGG[C/T]AGGAGAATCACCTGA | 7088 |
rs530208178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648248 | ACTGCACTCCAGCCT[A/G]GGTTACAGAGTAACA | 7088 |
rs530209329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605152 | CCGTGGGTATTTTTC[A/G]GAGAATTATTTGTAT | 7088 |
rs530246975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81598499 | AGAGTTCTTCAGGGG[C/G]AGGCAGAAGGTTTCA | 7088 |
rs530257901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81679778 | ATGGGGAGGGGAGAG[A/G]GTAGGAAACGAAATC | 7088 |
rs530280201 | snp | G/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689420 | CGGCCGTGCGAGGGT[G/T]GGGTGGCGCAGTCGG | 7088 |
rs530314226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610678 | GGGGCCGTCCTGGGC[A/G]TTGCAGGATGCTGAA | 7088 |
rs530316155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616590 | CACTGTTAGTTTTTT[C/T]TCATAACATTATTCA | 7088 |
rs530330171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648921 | TTGTTTTCTAAGGCC[G/T]AAGTGAGCTGTGTGT | 7088 |
rs530412933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632446 | AAACTTATACCAAAA[A/C]AGTTATCAGATTTAA | 7088 |
rs530413446 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688540 | GTGCGCGGGGGCAGC[A/G]CTCCAACCCCCGGCC | 7088 |
rs530414088 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81639666 | CGGCTCACTGCAACC[G/T]CCACCTCCCGGGTTC | 7088 |
rs530456532 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81621925 | TGCCAGGAGGCTTAG[-/AT]AAAAGCAGCTGGGAG | 7088 |
rs530458251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81654766 | ACCTTTCAAAGATGA[A/G]GCCTAAGGTGATAGA | 7088 |
rs530464022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647836 | AACACAATGTAAATA[C/T]TCCTATGTGGATTAC | 7088 |
rs530475462 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81639469 | ATTCTTCTATCTAGG[C/G]ATTAGTTTACAGTAA | 7088 |
rs530477888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645714 | CACTGCACTCCAGCC[C/T]GGGCAACAAGAGTGA | 7088 |
rs530481475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81595985 | CAAATCAAGCTGGGC[A/G]CCTCCAGGTAAGGCC | 7088 |
rs530487884 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600999 | GCAGACAATAAATCA[C/T]GGGATTTCTCAGTCT | 7088 |
rs530497764 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81676740 | TGAAGACAATTTACA[A/T]CTGCTATCTTAAAGA | 7088 |
rs530524888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81590055 | CCAAACTGCACCATC[C/T]GCAGGGACGGCTTCC | 7088 |
rs530547385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81601659 | ACCAATGATCTCCAC[A/G]GAGCTCAGGGGAATA | 7088 |
rs530555049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81633075 | AAGTGTATTTCCAAG[G/T]AAGTAATCACAGCAA | 7088 |
rs530620332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687539 | ATAAACATAAAGTTA[G/T]AAGTGGCTGAAAACG | 7088 |
rs530635025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682123 | GCCGGGCATGGTGGC[A/G]GACACCTGTAATCCC | 7088 |
rs530636181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645304 | GGAGGCAGAGGTTGC[A/G]GTGAGCGCCAAGATC | 7088 |
rs530649567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81595629 | CAAGACCATCCTGGC[C/T]AACAGAGTGAAACCC | 7088 |
rs530656177 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618662 | ACAGCAAAGCACAAA[C/T]GTTTCCAGGTATTAA | 7088 |
rs530668469 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81622756 | GCCCCATTCAACAGC[A/G]GACTTCAACAAGTTA | 7088 |
rs530676225 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667704 | AGTCCCAGCCCTTGA[A/G]CTGTATTCCTGCTCC | 7088 |
rs530690023 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599421 | CACATCGTGAGCAAC[A/G]TAAGGCATGTCGACA | 7088 |
rs530692208 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81612887 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 7088 |
rs530712422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651308 | TAGTGTGGAAGGGGA[C/T]GAACACATGAGAACC | 7088 |
rs530756215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81650696 | CTAAGTAACAGTCAA[A/C]AATGTGATACTGAAG | 7088 |
rs530761312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687168 | AGAGAAGAGGCGGCC[C/T]GGGAAGAACCAGGAA | 7088 |
rs530763822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609853 | GTGACAGCTGACTGC[C/G]CACAGCACAGCACTG | 7088 |
rs530790255 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623745 | CAATGAGCAGAGATC[A/G]TGCCACTGCACTCCA | 7088 |
rs530792370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81653278 | AACTTTCCACCCTGC[A/G]TGAAGATGCATTCAT | 7088 |
rs530844182 | snp | A/C/G | 0.000152263 | 0.00872413 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688169 | CCGCCCGGGAGAAGC[A/C/G]CCTCCCCAACGATCC | 7088 |
rs530876716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657071 | TGACCTCATTTTTAT[C/T]TGCATTACTTGAATT | 7088 |
rs530891112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662609 | GAGCTGAGGTGGTAG[A/G]ATAGCTTGAACCCAT | 7088 |
rs530991946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81585382 | ATATTAAAACAATAG[A/C]ATTATTGCATCCAGC | 7088 |
rs531010688 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81669595 | ATGCAAATATATGCA[C/T]GCTTACACCTCCACC | 7088 |
rs531013728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81614828 | ATCGGGGCATGCTCT[A/G]TGACATGCCCCGATA | 7088 |
rs531058130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609266 | ATTTTTGTATTTTTA[C/G]TAGAGACGGGGTTTC | 7088 |
rs531072530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652730 | AAGACAGGGTGAGCC[C/T]AGGAGTTCAAGACCA | 7088 |
rs531077493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81633942 | TGCAAACTTCCAGGG[C/T]GACCTGTGTTTCAGT | 7088 |
rs531135883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81663787 | ACCTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 7088 |
rs531136697 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643591 | CCCAGGTGGGATACA[A/G]TGGCATGATTTTATC | 7088 |
rs531178940 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81614066 | GTGCCCGCCACCATG[C/T]CCAGCTAATTTTTTT | 7088 |
rs531232884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620649 | ACTATTTTTGAAAGG[G/T]GATACCTACACAGCC | 7088 |
rs531239401 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689987 | GAGAGCGGCGGGGCT[A/G]GGCTGTCAATCAAAG | 7088 |
rs531243540 | snp | A/G | 3.34208e-05 | 0.0040877 | synonymous-codon, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81685715 | TCCATATGACATTTC[A/G]TAATACTGTAAAGAG | 7088 |
rs531274386 | snp | C/T | 1.68394e-05 | 0.00290162 | intron-variant | TLE1 | GRCh38.p7 | 9:81590788 | GAACCCCTCCTTAGA[C/T]GACCATCTTTGCTCA | 7088 |
rs531280098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81584725 | ATAATCTAAGAGGTA[C/T]CAGCCTCCTTAGTCA | 7088 |
rs531288777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612185 | GAAGCACAACCCACA[C/T]ATTTTCTCATTTGTG | 7088 |
rs531304195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588357 | TACGTGCCAACAGAG[C/T]ATGAGCTCATGTATT | 7088 |
rs531320944 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674793 | CACCTAATACAACCA[C/T]GCCAAAAGTACAAAG | 7088 |
rs531326297 | snp | G/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689636 | GCGGAGCCGGCGGGG[G/T]ACGTGAGCCCGGGAG | 7088 |
rs531340511 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586351 | TGTGAACTTCAGAGA[A/G]TGCACTTACACACAC | 7088 |
rs531350135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643720 | TTTTGATTTTCAGTG[A/G]AAAAAAAGTCTTGCT | 7088 |
rs531369516 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81660564 | GACTACAGGTGCCTG[C/T]TACCACACCCGGCTA | 7088 |
rs531510245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588018 | GGGAAACAGCACCTG[C/T]GATTGTCTTTCCCTG | 7088 |
rs531537732 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684491 | ATCTATGATGAATTA[A/C]AAATCAAAGAGTGCG | 7088 |
rs531545589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587444 | ATATGTAAATATAAC[A/G]GAGAACACACCTTAA | 7088 |
rs531574900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616863 | TAGTAATTATTATCA[A/T]CTTCCCCCTCTTCTC | 7088 |
rs531587233 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602807 | TGGGCATGAGAAAGG[C/T]GAGAATTTTAACAAA | 7088 |
rs531612815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656422 | CTTCTCGGAAATTCA[C/G]ATTGAAGGTTTCCAG | 7088 |
rs531643503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630698 | AGCAGCAAACAGCAA[C/T]TGGCTGACTTAATCT | 7088 |
rs531644723 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81618861 | TACCGGACCCTTCTG[A/C]AAATATAAACCTTCA | 7088 |
rs531648616 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81622907 | CAGCTGCCGGACGCC[C/T]GGCAGGCTTTCCACC | 7088 |
rs531676047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624519 | CATCAAGTAGAATTC[A/C]TTTTTCAAATATTTA | 7088 |
rs531741739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662978 | TCAGCCTCCCGAGTG[A/G]CTGGGACTACAGGTG | 7088 |
rs531788510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81594744 | ATATAATGTAAACAC[A/C]ATGAGTACTAACACA | 7088 |
rs531796446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81631859 | TGCAATCCCAGCACG[C/T]TGGGAGGCTGAGGCA | 7088 |
rs531817989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675320 | ATGGAAGACACTATG[A/T]AAAGACTAAGTAAAT | 7088 |
rs531825381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668817 | CATTAAATAAGGAGA[C/G]AGGAACTGAAGATAA | 7088 |
rs531872715 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81598889 | AAGCAACCAGAGGTC[A/T]CATGGAACAAGCTCC | 7088 |
rs531875863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588983 | AAGCCAAGACGTGAA[C/G]CATCACTTTTAAAAT | 7088 |
rs531879275 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629414 | CTGCACTTATATAAG[-/A]AAAAAACAGAAATCA | 7088 |
rs531882314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686165 | AGAACCTCTAACTGA[C/T]TCCTCCTCATGGTCA | 7088 |
rs531888066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669410 | ATATATTAATGAGGG[A/G]AAATAACCTTCTAAG | 7088 |
rs531907883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680834 | GCTTAACTCTAAGTG[C/T]CTATACTCTAGCTAG | 7088 |
rs531931622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81637758 | GAAATGTGGCCATTC[C/T]ACCTCATATTCGACT | 7088 |
rs531990291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586076 | AGGCTGGAGTGAAGC[A/G]GCGTTATCTCGGCTC | 7088 |
rs532022394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605987 | ACACTTCTCAAAAGA[A/C]GACATTTATGCAGCC | 7088 |
rs532051007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81627456 | ACAGACACCTCTACC[G/T]GGTACAGGCTCCTGA | 7088 |
rs532052319 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615282 | TGCAGTGTGCCGAGA[C/T]CACGCCACTGCACTC | 7088 |
rs532071260 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81632401 | CACAGAAGAGGGGGG[-/A]AAAAACCCTGAACTT | 7088 |
rs532091295 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81677707 | ACCAAACCCAGTCTC[A/G]TGGTACATGTATTTC | 7088 |
rs532092834 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81651894 | GAGGCTAAGGCAGGA[-/G]GATCACTTGAGTTCC | 7088 |
rs532099039 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610869 | AAGGATTCATACATG[A/G]ATTCCCTACTTTGTG | 7088 |
rs532112603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665188 | CAAACCGGGGGTGTA[A/G]GAACACATTTGCCTT | 7088 |
rs532142320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596636 | ATAGTGAGCATTCAT[A/G]AATATCGCTCACACC | 7088 |
rs532164558 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683369 | AATGCCCAGTTTCCC[C/G]CTAGAGAGAATTCCT | 7088 |
rs532180702 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81597019 | GGTCCACAGGCAAAT[C/G]AAGTGCCCAAACTTT | 7088 |
rs532180913 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657682 | GGTATCTGTGAGGGA[C/T]TGGTTCAGAATCCCC | 7088 |
rs532289964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672420 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 7088 |
rs532296843 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81609241 | AGGCACATACCACCA[C/T]GCCCAGCTAATTTTT | 7088 |
rs532300011 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681221 | TCATCCTTCCTTTCA[G/T]ATTTTCAGAGCTAGT | 7088 |
rs532306155 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81677317 | ACACCTGTAATCCCA[G/T]CACTTTGGGAGGCTG | 7088 |
rs532333274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81640790 | TACACACAGTCACAG[A/C]ACATGGCTTATCACC | 7088 |
rs532436921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81636288 | TAAAACTGAAGAAGC[C/T]TGCAGTGGCATCACG | 7088 |
rs532483347 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81661507 | GGGAAACTCCACCAG[-/C]CATTAAATTGCAAAT | 7088 |
rs532500251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81592174 | CCATTCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 7088 |
rs532517790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597739 | TTCACAGATGTAAAA[A/C]ATGAATGATATAAAA | 7088 |
rs532535960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81635491 | GAAATGAAAAAGTAT[C/T]CAAGAAATGGCCCCT | 7088 |
rs532551814 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81592336 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 7088 |
rs532622649 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660475 | CTGGAGAGCAGTGGC[A/G]CGATCTCGGCTCACT | 7088 |
rs532652059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622281 | TATCTTATTCAACTT[C/T]AAATCCGCCCAAGTG | 7088 |
rs532669431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604640 | CACGGTCAGAGGCAC[A/G]CTGTCACTGCACGAG | 7088 |
rs532748618 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687530 | GGGTGGGACATAAAC[-/AT]AAAGTTAGAAGTGGC | 7088 |
rs532751012 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685555 | CACAGGACAGGAAAC[C/T]AAGGCAGAAAAATAG | 7088 |
rs532760233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645231 | AGGCATGGTGGCGCA[C/T]GTCTGTAATCCCAGC | 7088 |
rs532784335 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81680969 | TAAGGTAAAATTTGC[-/AA]AAGAGTAAAAGAATC | 7088 |
rs532789789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638665 | GAGTCTTCACTGTTG[C/T]CCAGGCTGGAATACA | 7088 |
rs532820353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651227 | AGTGATTTGAATCTG[C/T]TCAAGGCACTCACAT | 7088 |
rs532911861 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81681487 | CCTGGGAGGCGGAGG[C/T]TGCAGTGAGCCGAGA | 7088 |
rs532944584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81595614 | ACGAGATCAGGAGAT[C/G]AAGACCATCCTGGCT | 7088 |
rs532964565 | snp | C/T | 5.2367e-05 | 0.00511671 | intron-variant | TLE1 | GRCh38.p7 | 9:81620967 | AACTGTAAGAGTCAA[C/T]GTGTACCACTCTAAA | 7088 |
rs533038928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624823 | TATTTACATCTCCTA[C/T]AGAAACTCAAAATAG | 7088 |
rs533052310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81606991 | CACTTTGGGAGGCCA[C/T]GGCAAGAGGATCACT | 7088 |
rs533056035 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625239 | GCATCTTCACTGGCA[A/C]CAAGCAAATTGCTAT | 7088 |
rs533057026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687143 | GAAACAATGGGAGGA[A/G]GAGGAGACAAGAGAA | 7088 |
rs533104004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81612823 | AGCACTTTGGGAGGC[C/T]GAGATGGGCAGATCA | 7088 |
rs533129490 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81614772 | TCCTGGCTTCCCCTG[A/G]GGCCTCCTTTGTGCA | 7088 |
rs533130498 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596042 | AATCTCAGATTTTTC[A/G]GAGAAAGGAGATTTT | 7088 |
rs533135949 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629024 | TTTTCCAAATAGTGA[A/T]CACACTAGCTAGGTA | 7088 |
rs533187432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687632 | CCGGCTTCTAAAGAG[A/G]CTCGGAAGCTCTTCC | 7088 |
rs533286045 | in-del | -/GTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603727 | GATACAAGGTCAGGC[-/GTG]GTGGTGGCTCATGCC | 7088 |
rs533286933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81630621 | AAGATCATGAGGCCA[C/T]AAGGCTTTGAAAATC | 7088 |
rs533298285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605059 | AGCATGCCTGGCATC[A/G]CACACAAAGCCTGAC | 7088 |
rs533307005 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81671028 | CCAAAATTAGCTAGG[A/C]ATGGTGGTGAGCACC | 7088 |
rs533326993 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584092 | CAAGGTTTGGAAACA[A/G]GTGTTTGTAATTTTT | 7088 |
rs533332735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663107 | CGCCTCGGCCCCCCA[A/G]AGTGCTGGGATTACA | 7088 |
rs533430173 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669744 | ATTTAGGCATTTCAA[G/T]CCTTAGATACAAAAT | 7088 |
rs533489968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81670312 | TTCTCACAATGCAAA[A/G]TCTACACAAAAGTCC | 7088 |
rs533555367 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672655 | CCCCACAGGTGTACA[C/T]ATCCCTCATCAAAAT | 7088 |
rs533565917 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81680458 | GTTCCTTGAAGATTT[C/G/T]GGGGGCATTCCGTTT | 7088 |
rs533577457 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81642509 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 7088 |
rs533578672 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81663734 | TTCACGCCATTCTCA[C/T]GCCTGCCTCAGCCTC | 7088 |
rs533592859 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584895 | GGATTAAACATCCAA[C/T]TTAAGTAAAATGCCA | 7088 |
rs533656801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603819 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 7088 |
rs533660577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610746 | AATCCATACCTGCCC[C/T]CCCTCCCACCCCCAG | 7088 |
rs533673364 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688721 | CCCGAGGCGGCGGCG[A/G]GCGAGGTGCAGGTGG | 7088 |
rs533715345 | in-del | -/TTC | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81681573 | AAAAAAGAAAAAAAA[-/TTC]TTCACCATCCTGGAG | 7088 |
rs533739218 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654336 | GTGACTATATATATA[C/T]ACACATATATATATG | 7088 |
rs533750753 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616896 | CTGACCTGGGGCTAG[C/G]CAAAGCTTCAGGCAG | 7088 |
rs533817121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672592 | TACTCTACTCACAAC[G/T]TTTGCACAGTACTTT | 7088 |
rs533852316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81621989 | AGTAATGTCTTTACC[A/G]CAGTGTTTGGGGATG | 7088 |
rs533875527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665503 | CTGAAAACAAGGAGG[A/G]GTTAAAAGAAAGGAA | 7088 |
rs533919596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81654251 | TGCACACTTCATTGT[A/G]ATAAGAGATGAGTAG | 7088 |
rs533935112 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681496 | CGGAGGTTGCAGTGA[A/G]CCGAGACTGTGCCAC | 7088 |
rs533992158 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673382 | AAAGAAATAAAACAC[A/G]GTAATGGGAAAATCA | 7088 |
rs534000320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81623208 | TCTTGAGGTGTTTTT[C/G]CCTCATGTTGTGATT | 7088 |
rs534036608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81623790 | GTGAGACTCTGCCTC[A/G]AAAAAATAATAAAAT | 7088 |
rs534038301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617036 | CTGAATTTCTCGAGG[G/T]ATGAAATCTTTAATT | 7088 |
rs534051394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628521 | TCTATAATGTTGTCA[C/T]TTTGAGACAAAGTGA | 7088 |
rs534064896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621566 | CAGACAATTATGTTA[A/C]CTTTCTCTGCCACAA | 7088 |
rs534091696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591872 | CTGTGTTTCCAAAAC[A/G]CCGCCACTCTGCTTT | 7088 |
rs534125076 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81629680 | GTATAGCCTACTACA[C/T]ACCTAGGCTACTGCT | 7088 |
rs534198101 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655247 | TGGGCGCCTGTAATA[A/C]CAGCTACTCGGGAGG | 7088 |
rs534217511 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597531 | TGGATAGAATCGTGG[A/C]AAACTGCAGGGCAGA | 7088 |
rs534252079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592231 | GGCGTGGTGGTGGGC[A/G]CCCGTAGTCCCAGCT | 7088 |
rs534294771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664021 | TCTCCTTCACAGGCA[A/G]AAAGAATGATGCATC | 7088 |
rs534333264 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TLE1 | GRCh38.p7 | 9:81667981 | TCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 7088 |
rs534365327 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81620712 | CTTTGATGGCAAACA[G/T]ATCTACAGGTTTACA | 7088 |
rs534383968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626082 | AGGAAAACCCATTCA[G/T]GCATACAGCAAAAGC | 7088 |
rs534392185 | in-del | -/AAAA | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81642706 | CTCAAAAAATGAAAG[-/AAAA]GAAAGAAAGGAAAGA | 7088 |
rs534460534 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81671185 | AACAAAAAAGAAACA[A/T]GGATGAATACAGATT | 7088 |
rs534463139 | snp | A/C | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586332 | TTGTTAGGTGACTTT[A/C]TTGTGTGAACTTCAG | 7088 |
rs534492558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678654 | ACTCCGTCTATACTA[A/G]AAACACAAAAAATAG | 7088 |
rs534496093 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611460 | CAAATAAAAAAAATC[A/G]ACTTTGGTGGGAGAA | 7088 |
rs534503098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81673234 | ACCAAGATTGCGCCA[C/T]TGCACTCCAGCCTGG | 7088 |
rs534506409 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81632102 | TCTCAAAAAAAAAAA[C/G]ACTATCTATAGGAAC | 7088 |
rs534539630 | in-del | -/ATT/ATTATT/ATTATTATT | 0.0447796 | 0.144252 | intron-variant | TLE1 | GRCh38.p7 | 9:81672322 | TCTCCCCTGCAATAA[-/ATT/ATTATT/ATTATTATT]ATTATTATTATTATT | 7088 |
rs534541252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632534 | TACTGCTATGTTCAG[A/G]AAGAAGGAGGCAAAA | 7088 |
rs534574004 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81645332 | ATCGCGCCATTGCAC[G/T]CCAGCCTGGGCAACA | 7088 |
rs534574771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81584839 | TCAGTCTCCTCATGA[C/T]AAAATGGGATTAAAG | 7088 |
rs534579421 | snp | A/G/T | 4.84696e-05 | 0.00492265 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634243 | CCCGAAGGGTGAGGC[A/G/T]TAAGGGGAACTGGGG | 7088 |
rs534666935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81672019 | ACTGGCAGGCTAGGG[A/G]GTTGTCAAGAACCTA | 7088 |
rs534715684 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81609980 | CTTTCCTCCCACCTC[A/G]TCCTCATCTCCAACA | 7088 |
rs534722564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620124 | GATCAGAGCATTACA[C/T]CAAGGGAGGCGGGGG | 7088 |
rs534766388 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81641134 | TGACAGTTCTCTCCA[A/T]ATCACTCTTCCTTGA | 7088 |
rs534775790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676162 | AAGTAGCTTTCACCT[C/G]ATTTTCAAACGTTCA | 7088 |
rs534798333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677437 | GGGCATCGTGGCAGA[C/T]GCCTGTAATTCCAGC | 7088 |
rs534825379 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583926 | GAAAGAATGGGCTGT[C/T]ATGTGAGTCGGCAGA | 7088 |
rs534828233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81596716 | CATTTCTAGAATTTC[A/G]AACACAGGCAAAATT | 7088 |
rs534875711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81652841 | TATTAAATCCGTTGA[C/T]TGGTTGATCACTTGT | 7088 |
rs534879100 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604684 | ACTTGAACCATGGAT[A/G]AGCATTTATACTAAA | 7088 |
rs534901598 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81600374 | CTAAACACAACTGAC[A/T]TCAAAAGGAAGGTCC | 7088 |
rs534909208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681263 | TTTTTAAATGCTTCA[C/G]CATCGGCCGGGCACA | 7088 |
rs534921536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81681902 | AGAGGCAGGCACTAG[A/G]GAGACATGGTCCACC | 7088 |
rs534935223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688018 | ACGTCAAGTAGGAAG[A/G]AGCCCAAAGGGAGGG | 7088 |
rs535032217 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637733 | ACTGCTGAAGATGTC[A/G]TGATTCTAGGAAATG | 7088 |
rs535034085 | snp | A/G | 1.6585e-05 | 0.00287962 | intron-variant | TLE1 | GRCh38.p7 | 9:81652319 | GAAGAAAGGGCATTA[A/G]CAACAGCCAAAAACT | 7088 |
rs535046141 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81593362 | GCTACGACTATGAAA[A/T]AGATGAAAAAAAGGA | 7088 |
rs535047363 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680475 | GGGGCATTCCGTTTG[A/T]ATTTTCAAAATATTG | 7088 |
rs535049365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634826 | GGTAACTCCATTTCA[C/T]CCTACACCCTTGCAT | 7088 |
rs535072806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674440 | GTTCCACACACTGGG[G/T]TCCTCAATGAGGTTT | 7088 |
rs535095781 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641662 | GACACACAAATGGCC[A/G]ACAGATATACAAAAA | 7088 |
rs535102264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596309 | ACGGGAAGCCCATAT[A/G]GATGTTAATACATCA | 7088 |
rs535109512 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621717 | GCCAGAGGTAATCAG[C/T]CAGGTGGCCAGCCCT | 7088 |
rs535181828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680069 | CGAAGGACGCTCCTC[A/T]ATTTGCACGCACGAG | 7088 |
rs535224573 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667955 | GATTGCCTGAGGCCA[A/C]GAGTTCGAGATCAGC | 7088 |
rs535242577 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639514 | TAAAAGTCAAAATGC[G/T]TGTAGATTTATACAA | 7088 |
rs535250471 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81682453 | ATCACATTGAAAACT[C/G]TTCATTACTGTGCAA | 7088 |
rs535256819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655305 | GAGGTGCAGGCTGCA[C/G]TGAGCCGAGATCACG | 7088 |
rs535277472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648565 | CCCTCGATTATCTGT[C/G]ATGTAAAGAGAACAA | 7088 |
rs535279271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609283 | AGAGACGGGGTTTCG[C/T]CACATTGGCCAGGCT | 7088 |
rs535281531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81602145 | ACTTCAACAGAAAGA[A/G]ACCAGTGAGAAGGGA | 7088 |
rs535285375 | in-del | -/A | 0.0217236 | 0.101931 | intron-variant | TLE1 | GRCh38.p7 | 9:81662540 | CTCTACTAAAAATAC[-/A]AAAAAAAATTAGCAG | 7088 |
rs535334427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604993 | CTTTTCTTTTAATGA[C/T]ATCATCAAGCCCCCA | 7088 |
rs535345864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609000 | AGCAACAACATTTGC[A/C]AAGATCTGCTGCCTT | 7088 |
rs535395889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81645137 | GGCCAAGGCAGGTGG[A/G]TCACCTGAGGTCAGG | 7088 |
rs535428049 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670321 | TGCAAAGTCTACACA[A/G]AAGTCCCTTCCCTTT | 7088 |
rs535459001 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662674 | TTGCACTCCAGCCTG[A/G]GCAACAAAAGTGAAA | 7088 |
rs535473892 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673500 | AGTTTTAAAGGGACT[A/C/G]CTATTTAGATCACAG | 7088 |
rs535476647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81631123 | CCACATTTGAACTAG[A/G]AAGTTCGTTGACTGC | 7088 |
rs535492807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643855 | TTTATTCTTTCTCCA[C/T]TTCAGCTAATCCACA | 7088 |
rs535500409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81607137 | CCAAAGGCCAATGGC[A/G]ATTTTGACCAAGATG | 7088 |
rs535503207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81636766 | TCCCAACACTTTGGG[A/G]GCCCAAGGCAAGTGG | 7088 |
rs535517503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605444 | TTTGACTTACGGGGC[A/G]GGGCGGGGAACTGGT | 7088 |
rs535526442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612525 | ATGAGTTTTTTAAGG[C/G]CTGGAGTCGCAGAGA | 7088 |
rs535531139 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690263 | TTGATGCTACTCTAA[A/G]AGTGAGGCCACATTC | 7088 |
rs535546246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618923 | AAGGTCTGAGGCCTC[C/T]GTTCCAGATTCTCCA | 7088 |
rs535561165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612983 | GAATCGCTTGAACCC[A/C]GGAGGCAGAGGTTGC | 7088 |
rs535593701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686412 | CTGCAATAAAGTGGG[C/T]TGAAGTTCTCCCTGC | 7088 |
rs535624955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649961 | GAAAAGAGCCTTCGG[A/G]CATAAATTCATATAC | 7088 |
rs535664836 | snp | C/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689647 | GGGGGACGTGAGCCC[C/G]GGAGGTTGGGGGGTG | 7088 |
rs535700180 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603890 | GCTTGTAATCCCAGC[A/G]ACTCGGGAGGCTGAG | 7088 |
rs535718854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610826 | CAAAATCATCCCCAG[C/T]TGCATACATGGGTCT | 7088 |
rs535723897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674798 | AATACAACCACGCCA[A/G]AAGTACAAAGGGCAA | 7088 |
rs535730295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81623944 | TCCTTTAATCTGGAG[A/G]ACTAGGATGTCCAGA | 7088 |
rs535744852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588241 | GTCTGTTCTTTAATC[A/G]TGCAGGCCTGAGTCC | 7088 |
rs535774021 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81594227 | CCTCTGGGCCACAAG[C/T]TGATTTCAAAGACAG | 7088 |
rs535817517 | in-del | -/CCCC | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81615894 | CCTCAAGCAGCAAAA[-/CCCC]CCCCCACATTTCCAA | 7088 |
rs535836258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81650878 | AGGAAATGAAGGTCA[C/T]CCTCCTAGTTTATTT | 7088 |
rs535836743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653514 | ATTAAGTTAATGTAT[C/T]TTGGACTATTATCAT | 7088 |
rs535874220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647220 | CTGGTCATCTGACGA[G/T]GTCTTCTAACTCTCT | 7088 |
rs535894360 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583952 | GCAGATTCCGTTCCT[C/T]AATCCTACAACCCAT | 7088 |
rs535895630 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688317 | TTTAATCCCGCCGAG[A/G]AAAATTAAGCCGGAA | 7088 |
rs535950481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609568 | AAGAATAGCCAATTG[A/C]GTTTTTTTAAATTCC | 7088 |
rs535959337 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690851 | AGTTAGGTAAATGAC[C/G]TGGCTAAGGTTCTTA | 7088 |
rs536021456 | in-del | -/TT | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81632255 | CATTTTCCAGAGAAA[-/TT]TATAGGACAAGAATT | 7088 |
rs536040813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624579 | AGCTTTTTGATCAAC[A/G]TGAGAACCAGTGTTA | 7088 |
rs536066014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656022 | AATTCTCCCTGACCA[C/G]CAATGAGACAAGGTT | 7088 |
rs536076033 | snp | C/T | 6.85252e-05 | 0.00585303 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688269 | GCCGGGGCTCTGTTC[C/T]CCGGCAACTCAATTC | 7088 |
rs536110854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631552 | AAAGGGCTTTGTTGC[A/G]TGCTTACATACCTCG | 7088 |
rs536147915 | in-del | -/TTGGGAGACTCTTTGTTTCCTTATTTAGAGGCATACACTCTATTT | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81599853 | CTTCAAAGCATTAGG[lengthTooLong]TTGGGAGACTCTTTG | 7088 |
rs536170751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81675256 | TATTGCTGTGTATTT[C/T]TCTTTTATTCTGTAA | 7088 |
rs536181885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81649748 | AACAGACAGTTTCCC[A/G]GTACCTCCTCCCCTC | 7088 |
rs536187038 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669260 | CGAAGGCTGTGAGAA[C/T]GCTGCAAATGGCTTG | 7088 |
rs536189277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81661492 | AAGTCAGCTTAGGGA[A/G]GGGAAACTCCACCAG | 7088 |
rs536251559 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644758 | CAGCACTTTGGGAGG[A/C]AGAGACAGGTGAATC | 7088 |
rs536258547 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81660571 | GGTGCCTGCTACCAC[A/C]CCCGGCTAATTTTTT | 7088 |
rs536290909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588277 | AGAAAGAAATGGGGA[C/T]GTTACAAGCACAGGG | 7088 |
rs536315475 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606309 | TCATGCTGCTATAAA[G/T]ACACATGCACACATA | 7088 |
rs536327001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673216 | AGGTGGAGGTTGCAG[C/T]GAACCAAGATTGCGC | 7088 |
rs536365853 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688078 | ACCCCAGGAAGAGAG[A/G]GCCCCAGACCTCCCC | 7088 |
rs536378957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659569 | ACAAGACTTTCTTCA[C/T]GGATGGCCACCACCT | 7088 |
rs536381576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81666592 | CCAGCCTGACTAACA[G/T]GACGAAACGCAGTCT | 7088 |
rs536426721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664851 | CACCTGCGGAGTTCC[C/T]GTTGGAGTCTAGGCC | 7088 |
rs536427756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81642290 | GATTCTGGATTTTTT[G/T]CAGATTTTTAAATAT | 7088 |
rs536438938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620823 | TCTGTCCTATTTACT[A/G]TTTGAGAAATAGGAG | 7088 |
rs536449373 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630232 | CGGAGACCCTCGCAA[A/C]TCTATGAGGGCAGAT | 7088 |
rs536451800 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81662111 | TCAAAGCGAAAAGAG[-/A]AAAAAAACAGGTAAA | 7088 |
rs536462062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659129 | GGCCAGGATGGTCTC[A/G]ATCTCCTGATCCTCG | 7088 |
rs536506845 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634203 | GGCACTGCCCCCGAG[A/G]GGCGGGATTCCAGGA | 7088 |
rs536524185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671335 | CCTGGGCAACATGGC[A/G]AAACCCTGTCTCTAT | 7088 |
rs536531951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81603744 | TGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 7088 |
rs536568407 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81597267 | ACAGTATTGTTATCG[C/T]ACCACCACGACTTAA | 7088 |
rs536582287 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81585110 | GAGTGTAACTAAGTG[C/T]CTGCGTATACCTAAA | 7088 |
rs536585964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664311 | TGTACCAAAAATGAT[A/G]CACACAAAACACTGC | 7088 |
rs536589345 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81641861 | AACCCAGTGTCTACT[A/C]AAAATACAAAATTAG | 7088 |
rs536598188 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81662691 | CAACAAAAGTGAAAC[C/T]CCGTATCAAAAAAAA | 7088 |
rs536616825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81670407 | CTTGGCTCACTGCAA[C/T]CTCCGCCTCCCGGGC | 7088 |
rs536619604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587603 | ACCATCCTAGGGTAA[A/C]GGAGGGAGGGTTGTG | 7088 |
rs536641770 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81630236 | GACCCTCGCAAATCT[A/G]TGAGGGCAGATTCTC | 7088 |
rs536646906 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | TLE1 | GRCh38.p7 | 9:81584229 | TAGACTGTAGCCTTC[C/T]TGTCCCCCGAGCCAG | 7088 |
rs536652654 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605139 | CCAAGCATTCTTTCC[G/T]TGGGTATTTTTCAGA | 7088 |
rs536676445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81625968 | GCCCTGTCAATGCTA[C/T]CAAACACTAGTTACA | 7088 |
rs536738792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586336 | TAGGTGACTTTATTG[A/T]GTGAACTTCAGAGAG | 7088 |
rs536743988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588754 | GGGAGGCAGCCAGAA[A/G]AGGCGAGCAAAGTCT | 7088 |
rs536776979 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656601 | CCAGGTTCTCACTTA[C/T]GTGCACAGAAGCCCA | 7088 |
rs536791467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673591 | CACTTAATCTTGGTA[A/G]TTACCCTATGGGGTA | 7088 |
rs536798284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81600290 | ACTACATTTATATCC[C/T]ATAAACCAAAAGTCA | 7088 |
rs536805053 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81678590 | GAGGCTGAGGCACGT[G/T]GCTCACTTGAAACCA | 7088 |
rs536809868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675025 | AAATTTTAAAAAAAG[C/T]ACATGGAAATCCCTG | 7088 |
rs536817005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81597513 | AGAGTAGAGATGGAC[A/G]TTTGGATAGAATCGT | 7088 |
rs536819224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672905 | TACTGATAGTTACAT[C/T]ACTTAAAGCTATTGC | 7088 |
rs536827805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592290 | GTAAACCCCGGAGGC[A/G]GAGCCTGCAGTGAGC | 7088 |
rs536831404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644803 | GTTTGAGAACAGCCT[A/G]GCCAATATGGTGAAA | 7088 |
rs536855935 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681837 | CATACATTCAGTCCT[G/T]ACATGTCTTACAAAT | 7088 |
rs536860685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638820 | AGTAGAGATGAGGTT[C/T]TACCACATTGGCCAG | 7088 |
rs536869638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631710 | CAATAGATTTAAAAC[A/G]CATAACAGCCTAAAG | 7088 |
rs536870368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628809 | TTGATAAAACCATGG[G/T]GCTGTGCCATATGAC | 7088 |
rs536946623 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81684379 | CATTTTTAAAGGCCC[A/T]ATTACATTATTAATA | 7088 |
rs536976835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604251 | CTCCCGGTGGGGTCC[C/T]CTATGCCTATGCAGG | 7088 |
rs537017044 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583770 | AAAAATACAAAAAAA[A/C]ATTTCACAAGATGCA | 7088 |
rs537039503 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81625183 | GGACTCTCTCTCTCA[C/T]GAAAATCTGGAATTC | 7088 |
rs537135763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81608779 | CCATCTCTACTAAAA[A/G]TACAAAAATTAGCCA | 7088 |
rs537136859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682056 | TTCGAAACCAGCCTG[C/T]GAACATGGGTGAAAC | 7088 |
rs537137288 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687678 | ATTGCGCTAAGTGCG[C/G]CCGGGTCACCAGGCC | 7088 |
rs537151402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682424 | AGGATGCCTATGGAG[A/G]TCACAGAAGACAAAT | 7088 |
rs537170472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602036 | TCATAAGATGTTTCA[C/T]GGTGCAACTGGAGGG | 7088 |
rs537190176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81636331 | TGCTCATTAGCACTT[A/C]ATTAGGAACTAGACA | 7088 |
rs537279087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681144 | TTACATGGCCTGAGA[C/T]GTTGCTTGCTGAAAT | 7088 |
rs537337730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656569 | TAACATATTGGTGAT[G/T]TTAGGATACCATCAT | 7088 |
rs537337845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663214 | GCTCACCACGTTTGC[C/G]ATCAACAGTGGTGCT | 7088 |
rs537338831 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81606475 | TGTCCTTTGCAGGGA[C/T]ATGGATGAAGCTGGA | 7088 |
rs537344598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680596 | CCACTGGCCCACTGC[C/T]GAAGGGTGGGGAAGG | 7088 |
rs537365196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686845 | CTTTATACTATTATA[C/T]CCACCTCCCTCACCA | 7088 |
rs537378973 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81664813 | GATGGTCTTGTGCTT[C/G]TTAATACACAGATGA | 7088 |
rs537415600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676954 | TGTAACTTACAAATT[C/T]GGCCGGGCATGGTGG | 7088 |
rs537423113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81640079 | TGGTGCATCTAATGG[C/G]TGAAGGCCAAGGATG | 7088 |
rs537434349 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625101 | CATAACTTTTATATA[G/T]AAAGTACTTGAGATG | 7088 |
rs537452329 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601067 | TCTCCATATCCATAT[C/T]TATAGTTTATTGGTT | 7088 |
rs537459018 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TLE1 | GRCh38.p7 | 9:81672868 | TCCCTTTAAATGAAA[A/G]AACTCAACACAACTT | 7088 |
rs537460255 | snp | C/G | 9.91686e-05 | 0.00704092 | intron-variant | TLE1 | GRCh38.p7 | 9:81633338 | GTGCAGCAGGCGTTT[C/G]AGTACTTACTGTGCC | 7088 |
rs537468897 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81626187 | TGGGAACTTTCTCCT[-/C]CCCCGCAGGAAAAGT | 7088 |
rs537477625 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81679303 | TAAAAATTTTTCTTC[A/C]CTTTTTTTTCTTTTT | 7088 |
rs537506809 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689153 | TTCCTCGGTCTTCTT[C/T]CTTTCCTTCCTTCAC | 7088 |
rs537539431 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81601323 | TTCCTATGAGGCAAT[C/T]TTACCCCAAACGTAG | 7088 |
rs537564554 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81597614 | CTCAGAAAGCCTCAG[A/T]ACTGAGACCCAGCCC | 7088 |
rs537584546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639583 | AAAAGTTGTTTTTTT[G/T]TTTTGTTTTTTTTTT | 7088 |
rs537611750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81654328 | TTAATATGGTGACTA[C/T]ATATATATACACATA | 7088 |
rs537616554 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81651564 | ATTGGTGTGTGACTT[A/T]AAAATTCATGAAAGA | 7088 |
rs537653282 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81645569 | AACATGGAGAAACCT[C/T]GTCTCTACTAAAAAT | 7088 |
rs537683459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610760 | CCCCCTCCCACCCCC[A/T]GTTATGATAATCAAA | 7088 |
rs537696674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81607918 | TAGTGTAGACAAAAA[C/T]CTCATTTCATAATGA | 7088 |
rs537713248 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81613203 | CAGAGTGCAGCTGCT[A/G]AAACCCCAGGACAAA | 7088 |
rs537750454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613620 | TGGGCACCTTCTAGC[C/T]ACTCCCTCAGCCAAT | 7088 |
rs537778502 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640015 | TCCCTGCTTCAGGGA[C/T]ATATGGCCATGTGTG | 7088 |
rs537779577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81660085 | TTCCATACAGTTTCT[C/T]AACAGCTTTCTACCT | 7088 |
rs537821740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643125 | GTTTCAGTTACCCAA[C/G]ATAAAGAAGATCTGG | 7088 |
rs537864902 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653151 | TTGTCATATCAGACA[A/G]ACAAAGGTTATGGTG | 7088 |
rs537899296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612466 | CTTTGGGCCCAGGTT[A/G]TTGCTTTTTTCCTTT | 7088 |
rs537911976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617610 | AGGCAGCTGAGGCAC[A/G]AGGATCGTTTGAACC | 7088 |
rs537921477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611321 | GTTTAAAGTGTAACA[C/T]AGGCATAGAAAGAGA | 7088 |
rs537949309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618166 | TACAATGTAGGCATA[C/T]GGAAAAAGCAGGACA | 7088 |
rs537978002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81642554 | AAAAAATTAGCCAGG[C/T]ATGGTGGTGGGTGCC | 7088 |
rs537981883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655473 | GGAACAGAGGGTACT[C/T]TACTTCTAGCCCAGG | 7088 |
rs537982466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648385 | AAACTGTAAGAATAA[C/T]GGAATTCACTGGGGT | 7088 |
rs537993789 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668219 | GAAGTTGTGGTGGGC[A/C]AGGGTAGGGATTAAA | 7088 |
rs538006194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612930 | AGGCGTGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 7088 |
rs538039370 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81623314 | GCTACTTTATACATA[C/T]TTCGAGAATTCAGAG | 7088 |
rs538044955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648000 | TTTATGGGCAGGCAC[A/G]GTGGCTTACACCTGT | 7088 |
rs538055402 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81670552 | ACTGGTCTCGAACTC[C/T]TGACCCTCCTGACAC | 7088 |
rs538090987 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586218 | AAGACGGGGTTTCAC[C/T]GTGCCAGCCAGGATG | 7088 |
rs538108967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630483 | ATCTGTTTAAGTGAT[G/T]TAATTTTCTTTCTTA | 7088 |
rs538112616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622482 | GATGTCAAATGGTAC[C/T]GTGAACGTAAAAGTA | 7088 |
rs538142017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592681 | GGTCAATTAAAAAAC[A/G]AGTGGATGGCAGGGA | 7088 |
rs538177459 | snp | C/T | 6.69613e-05 | 0.00578586 | missense | TLE1 | GRCh38.p7 | 9:81593258 | GACCGTCTGCAGTAA[C/T]GTGGAAGGAGTATGC | 7088 |
rs538180777 | snp | A/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690686 | GAACTTCTCAGCTAC[A/G]AGACTACGAGTCTGT | 7088 |
rs538184649 | snp | A/G | 3.29919e-05 | 0.00406138 | synonymous-codon, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587807 | AATACAGCTGGCTCC[A/G]TCTGTGTGGCCCTGG | 7088 |
rs538204375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655978 | AAAGTCTTTGGTTTT[A/G]TAAGATTGGATTTAG | 7088 |
rs538225280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81659056 | TGGGATGACAGGCAC[A/G]CGCCACCACACCTGG | 7088 |
rs538239755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649939 | AATTATTGATCACCA[C/G]AAACTTGAAAAGAGC | 7088 |
rs538293074 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81682093 | CTACTACAAAAAAAA[-/T]GAAAAAAAAAGTTAG | 7088 |
rs538332218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81661353 | CACTCCTCAGCGCCC[A/G]CACACTTCCCCACTA | 7088 |
rs538357314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621423 | TGCAAGGGGGCAATT[C/T]GTTCAGTGATGTGTT | 7088 |
rs538414180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668081 | GAGGCATAAGAATTG[C/G]TTGAACCCAGGAGAC | 7088 |
rs538436830 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81628433 | TGAACGTGATTTTTC[-/T]TTTTTTTTTCCAGAA | 7088 |
rs538452416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81633260 | TGTCTGTCTGTGCCT[C/G]TGTGGAGAAGTGTTG | 7088 |
rs538456428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81584920 | ATGCCAGTCACATCA[C/T]ATAGCATGAAGAAAA | 7088 |
rs538483336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626719 | TTAGGAGGACTCATG[G/T]AAAGATAGCTGTGCA | 7088 |
rs538493184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81637273 | TGAGGTGGGAGAATC[A/G]CTTGAACTTGGAAAG | 7088 |
rs538517787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81640042 | TGTGGAGGTCACTGC[A/G]GGGGAGGGAAAAGAA | 7088 |
rs538539444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81595711 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 7088 |
rs538549196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81667454 | CTAACACATTTAAAT[A/C]TTCAGCCAATCTAGA | 7088 |
rs538550647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682312 | GGAGGCAACCCAACT[C/G]AAGCTTCAATAGATG | 7088 |
rs538574183 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655108 | CGGTGGCTCGCGCCT[A/G]TAATCCCAGCACTTT | 7088 |
rs538576231 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81596121 | ATTAAATAGATGCAC[A/C]GAGTAACAGACGGGA | 7088 |
rs538665982 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81609074 | CCCCTCCCCTTTCCT[C/T]TCCTCTCCTTTCCTT | 7088 |
rs538705301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588421 | CTGCATTAGGAAATC[C/T]GGACTCCCAGAGACA | 7088 |
rs538709932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81634863 | ACCACAGTAGTATGA[C/T]GAGACAAAACCAAAA | 7088 |
rs538754840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81658264 | AAACCATGGTTAGCT[C/G]AATTCACAGATGCAG | 7088 |
rs538755707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677947 | GAAGATGAAAAAGTT[A/C]ATTCAACGGATAGAA | 7088 |
rs538786806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591985 | GCAGACACCACACCA[C/G]GGCAGGGCAGGGCAG | 7088 |
rs538824658 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81641307 | ATCAAGGACACTACT[A/G]CAGGAGTTATCGCAA | 7088 |
rs538826426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647188 | CTGGCATTTTGTGGA[A/C]GGGAGGACAGTCCCC | 7088 |
rs538862741 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81641761 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 7088 |
rs538886796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632623 | TGAGACACACTTTAA[A/G]TACAGGTCTCTCCAG | 7088 |
rs538898951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683580 | TATTAATGTGTGACA[C/T]TCAGAAGGATGTTTT | 7088 |
rs538941044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609334 | AGGTGATCCACCCGC[C/T]TCAGCCTCCCAAAGT | 7088 |
rs538948844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589854 | GCTCACCTACACTAC[C/G]CAGCAAACAGAAGAG | 7088 |
rs539005918 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614073 | CCACCATGCCCAGCT[A/C]ATTTTTTTGTATTTT | 7088 |
rs539041921 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665490 | CACTCGCAGTTCTCT[A/G]AAAACAAGGAGGGGT | 7088 |
rs539052476 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642335 | CTGGCTGAGAATTAG[A/G]GCTGCTCAATCTGTA | 7088 |
rs539059110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629418 | CACTTATATAAGAAA[A/T]AACAGAAATCAAAAT | 7088 |
rs539098290 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81631964 | AAAATTAGCCAGGTG[G/T]GGTGGCACAGGCCTG | 7088 |
rs539154358 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674960 | AGGAATTCGAGACCA[A/T]CCTGGACAACATAGT | 7088 |
rs539230782 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81649769 | TCCTCCCCTCTGGGG[A/G]GACAGGTTGACACAC | 7088 |
rs539256625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81677496 | TGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 7088 |
rs539269458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644411 | AAAATACTGGTGATA[C/T]GACAACATGGATAAA | 7088 |
rs539300601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688031 | AGGAGCCCAAAGGGA[C/G]GGAGAAAATTAAGAG | 7088 |
rs539322280 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595105 | GGGAACCATGGAGAC[C/T]GTCCTGGGGAATAAA | 7088 |
rs539343241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683021 | CAGGAAAGGAAACCA[C/T]AATTATACCATTCTT | 7088 |
rs539352893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81602933 | ACAAAGAGAAGAAGT[C/T]TGGGGAGGCTGGAAT | 7088 |
rs539475278 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81624649 | CAAAGTTTTATTTCA[C/G]CTTGCAGCTGGTAAA | 7088 |
rs539481961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638032 | TAAGAAAGGAAAAGG[A/G]CAAAGCCATTCTCTA | 7088 |
rs539509606 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687031 | TCAGCTCAGTCTGCT[A/G]AAAAATAAATACATG | 7088 |
rs539516338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680541 | CCATGCCCAGGGACT[C/G]CCTTGCCTTACTCCA | 7088 |
rs539524090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81607282 | CTCACAAGCCAAGGA[C/T]ATGAATACTTTAATA | 7088 |
rs539528475 | snp | A/G | 3.29511e-05 | 0.00405887 | missense | TLE1 | GRCh38.p7 | 9:81613478 | ATGTCGCTCCGAGGC[A/G]TTGGTGTGCTGGATT | 7088 |
rs539530790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599728 | TTGGCCATTTGCGTA[C/T]TCTTCCAAATAGAAA | 7088 |
rs539550404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81594416 | AAACCATCATTCCCA[A/G]CAAACTAACACAGGA | 7088 |
rs539559623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81600680 | GATGGTCAATTTTAT[A/C]TGTCAACTTGATTAA | 7088 |
rs539594558 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594929 | CATAAAAGCAAAATA[C/T]CAGACACATGAAGAC | 7088 |
rs539644427 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686860 | CCCACCTCCCTCACC[A/G]TCACCAATGATGGGC | 7088 |
rs539669693 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639110 | TAATTTTTTTTTATA[C/G]AGATGGGGTCTCACC | 7088 |
rs539700069 | snp | A/G | 4.53443e-05 | 0.00476131 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611796 | CCCGTAGGCCACCAC[A/G]GCGGCCGCGGCGGCT | 7088 |
rs539705519 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689709 | CGCGTGCGCTGCAAC[C/T]AACGTGGGGCGCTGA | 7088 |
rs539718923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618305 | AATATTAGTACAAAC[A/G]AGTGCAAATATTATC | 7088 |
rs539726307 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81669556 | GCAGTGTAGGGGCAT[A/G]TGCCAAAATCTCCTC | 7088 |
rs539762183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81605569 | ATGGGCAGTCATACG[C/T]AGAAAGCTGAAACTG | 7088 |
rs539796257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81591592 | CTTTCCATCAAAACC[A/G]ACACATATGAAGGGG | 7088 |
rs539832229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81634531 | TTCACCTGCTCAATT[A/G]CCTCTCCCACCTTCC | 7088 |
rs539843426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639571 | AAAGTGATTAGTAAA[A/C]GTTGTTTTTTTTTTT | 7088 |
rs539853562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681943 | GATGGCAGCATGAGG[C/G]GATAGGAAGAAGCAC | 7088 |
rs539866452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628288 | CATTTATAGATGGGA[C/T]TAGGAAGGCACAAAA | 7088 |
rs539878194 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600075 | CCTCTATCAATTACA[C/T]GTTTCCAAACTTCTC | 7088 |
rs539902524 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676958 | ACTTACAAATTTGGC[C/T]GGGCATGGTGGCTCA | 7088 |
rs539970575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596980 | TCGAGGGGAAGGCTC[A/G]TAACCAGTTAACACA | 7088 |
rs539984906 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667403 | AAAAAAAAAAAAAAA[A/G]AAGAAGCAAAAATCA | 7088 |
rs539985224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81651480 | AGGAGAGCAGAACCC[C/T]GGTGAAAAGCCAGGG | 7088 |
rs539991094 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656520 | AAAGAAAGTTAAAAT[A/T]ACCCTGAGCCCATCA | 7088 |
rs540043628 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662455 | ATCCCAACACTTTGC[A/G]GGGGCCGAGGTGGGT | 7088 |
rs540048800 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678006 | TTTTTCCTTCTACCC[-/A]AAGTGACTTGTATCC | 7088 |
rs540062533 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81649503 | CCTTAAAGGGAATGA[C/G]AATGTTTCGGCTCAT | 7088 |
rs540065946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81613132 | CTGGGGGGACAAGAG[C/T]GAGACTTCGTCTCAA | 7088 |
rs540079050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602427 | TCATCTTGGGGATGG[C/G]ACCCAGTCTAAACAC | 7088 |
rs540096921 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81619755 | ACAGAGCCAATGGCC[A/G]TCTGGCTTGGTTTGG | 7088 |
rs540099734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688108 | CAGCCTTACACCGCT[C/G]AGGGCGAGAAGGTCC | 7088 |
rs540125272 | in-del | -/TAAAATAAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645764 | TAAAATAAAATAAAA[-/TAAAATAAAA]ATAAATGCTTGAGGG | 7088 |
rs540141533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609227 | GTAGCTGGGATTACA[A/G]GCACATACCACCACG | 7088 |
rs540146477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619132 | ATGTCATAAACCTTC[C/T]AACTTGCTTATTAAC | 7088 |
rs540201855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648160 | GCCTGTAATCCCAGC[C/T]ACTCGGGCGGCTGAG | 7088 |
rs540210803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81641925 | TACTCAGGAGGTTGA[A/G]GCAGGAGAATTGCTT | 7088 |
rs540230457 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631152 | GCTAACCCTAACTTA[C/T]AGACTTACAAATAAC | 7088 |
rs540240852 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81648636 | CAATATCTATCAGAG[C/T]AGGTAGAAGAGAGCT | 7088 |
rs540262451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678135 | CTATGAGACCTTACA[G/T]GGGAGGGGATAAACA | 7088 |
rs540264483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81672378 | CACTCTTTTTGCCCA[A/G]GCTGGAGTGTGATGG | 7088 |
rs540271422 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81642647 | TGCAGTGAGCCAACA[C/T]GGTGCCACTGCACTC | 7088 |
rs540295651 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601270 | CTTTTTCTTGGCTAA[A/G]AGCCTGGAAAGGGTC | 7088 |
rs540317249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684703 | TTGTATTGTTGCACT[C/T]TGAAATGTGTCCAAC | 7088 |
rs540333541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610509 | TTTGGGAGGTAGAGA[A/G]GAGATGTGATCTATT | 7088 |
rs540344548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683757 | GTTTTTCAAATTGCT[A/G]AGCCAATTATACACA | 7088 |
rs540357731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81654604 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 7088 |
rs540362200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629027 | TCCAAATAGTGATCA[A/C]ACTAGCTAGGTATTT | 7088 |
rs540399944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653092 | GAGCCGTGGATCACT[A/G]AAGTCTAACAACTAC | 7088 |
rs540418176 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TLE1 | GRCh38.p7 | 9:81677738 | AGTAGTTTGACAAAC[C/T]GCAAGATTTGGACGC | 7088 |
rs540448219 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650679 | TGTGATTAGAGAGCC[C/T]ACTAAGTAACAGTCA | 7088 |
rs540460486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622693 | GAAAGTTCCTCTAAA[C/T]GTGGTGGACAGGGCT | 7088 |
rs540485166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628899 | TTGATGAGTTATAGT[C/G]TCTCCCCAGAATTCT | 7088 |
rs540498239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615833 | ACCCTGAATGGTGAC[A/G]AAGAACAGAAGGATG | 7088 |
rs540566479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652577 | GATAACATAGGACCT[C/T]AAAAAATAAATAGAA | 7088 |
rs540587899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665732 | TTCATTTTTAATAGC[G/T]GGCTTGAGTGTGGGG | 7088 |
rs540613017 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688980 | TGTTCTCCGCGGTTG[C/T]ACAAACCCTCCGGGC | 7088 |
rs540616661 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672759 | AAATTTTCCATGTTA[C/T]ATTCGAAAGAAAAAC | 7088 |
rs540632695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651608 | ACAAGAGCCAACAGT[G/T]CTATAGGTTCGAATA | 7088 |
rs540636514 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81592202 | CTCTACTAAAAATAC[-/A]AAAAAATTAGCCGGG | 7088 |
rs540669376 | in-del | -/AGGAGGAGG | 0.00158902 | 0.0281422 | intron-variant | TLE1 | GRCh38.p7 | 9:81634330 | TGGTGAGAGAGAAAA[-/AGGAGGAGG]AGGAGGAGGTAGTGG | 7088 |
rs540669587 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81604623 | CCCCATCCTTGGACA[C/T]GCACGGTCAGAGGCA | 7088 |
rs540680066 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689267 | GGGAAAACAGCAGGA[A/G]TGCGCTCCGCCAATC | 7088 |
rs540687173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616478 | TAAAACTTTATGTCA[C/G]TTAGACCATTATTGC | 7088 |
rs540721716 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81656301 | TCTGCACTGTCTATT[A/T]GAGTGCATGTAAAGG | 7088 |
rs540722842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610868 | TAAGGATTCATACAT[A/G]GATTCCCTACTTTGT | 7088 |
rs540780040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674479 | GTCCTTACCCCCTTA[A/C]CACCCAAGGTCCCTG | 7088 |
rs540790330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81666638 | AAATTAGCCAGGCGT[A/G]GTGGTGCACGCCTGT | 7088 |
rs540835677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669798 | TCATCATTTAAGCCA[C/T]AGAATAAATAAATGT | 7088 |
rs540854022 | snp | C/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589054 | TCCAGGTTGAGTCCT[C/G]TCTCCTGCGGCCGTG | 7088 |
rs540883436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631825 | GATGACTATCTCACC[A/G]GGCATGGTGGCTCAG | 7088 |
rs540910919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592085 | GGAACATGGCCGGGC[A/G]CGGTGGCTCACGCCT | 7088 |
rs540916390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585980 | CATATATCACCTATC[A/T]AGGGGGATACATTCT | 7088 |
rs540922719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81673003 | CAAGGCCGGACGCGG[C/T]GGCTCACGCCTGTAA | 7088 |
rs540925861 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81624355 | AACACTGAAAAAGGC[C/T]TCAGCAGAGTGACAA | 7088 |
rs540950412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81594539 | CAAGAGCAAGACTAC[A/G]TCTTAAAAAAAAAAA | 7088 |
rs540960403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668442 | TGCCATGGTGTATGG[A/T]TTCACAGAATATTGA | 7088 |
rs540974322 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655706 | AAGGATCACAAGAAA[A/G]AAACTTAAAAGCACG | 7088 |
rs541006858 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691051 | GTGAATGAATAATGC[A/T]GGTTTAGCCAAACGG | 7088 |
rs541023649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664453 | TGCCTTGCTCACCAA[C/T]AGCTCATGAAAAGGT | 7088 |
rs541050895 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630066 | ACCCACATTCCCTGC[A/G]GATCCCATCAGTCTC | 7088 |
rs541067990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687120 | GAACAGTGCAAACCG[A/G]CAAAAGGGAAACAAT | 7088 |
rs541071544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81607366 | CACACATATAAGGAA[C/T]AGGGTCCAATTTAAC | 7088 |
rs541094320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612725 | GTTCAAAATAATTAT[C/T]AGAAACTTTACTGAA | 7088 |
rs541118550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676991 | CCTATAATCCCAACA[C/T]TTTGGGAGGCCAAAA | 7088 |
rs541127064 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583906 | ATCCCCAGATCACCC[A/G]GAAAGAAAGAATGGG | 7088 |
rs541132685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81671403 | TGTAATCCTAGCACT[C/T]TGGGAGGCCAAGGTG | 7088 |
rs541162145 | in-del | -/TAAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680660 | ATAAGAAACAAAGGC[-/TAAT]TAATCTTGCACCTCG | 7088 |
rs541178379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662241 | AGTTAAATACGCTAC[A/C]CACCAACCCACAGGC | 7088 |
rs541186438 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583303 | GGGAAAAGGAAGAGG[A/G]GATTGGGCCTTCCTA | 7088 |
rs541259525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676674 | CACAGGGGGAAGTCA[A/G]AATTTAAAAGAACAC | 7088 |
rs541286042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681481 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 7088 |
rs541326318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675169 | GGAGCCTATGGAAGA[C/T]ATATGACAGATAGAT | 7088 |
rs541346097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675988 | ACGGGCGTGAGCCAC[A/C]ACACCAGGCCGACCC | 7088 |
rs541381025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682092 | CTCTACTACAAAAAA[A/G]AGAAAAAAAAAGTTA | 7088 |
rs541386022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587978 | CTGATGTGCAAGATC[A/T]AACTAACCTTCCCCT | 7088 |
rs541405459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645587 | CTCTACTAAAAATAC[A/T]AAATTAGCCAGGCGT | 7088 |
rs541432537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626862 | CAAAACAAACTCTGG[A/G]GCAGACAATAAATAC | 7088 |
rs541491256 | snp | C/T | 4.94784e-05 | 0.00497361 | intron-variant | TLE1 | GRCh38.p7 | 9:81616639 | CTTTGATGAAAAGAA[C/T]GGTTACCTCATTAGA | 7088 |
rs541494116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81633438 | ACAGAAATAAAAAAA[A/G]GGGGGGAATAATTAG | 7088 |
rs541497969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626369 | CACATCTGTGTGCCT[G/T]CTCCATCTACACCTG | 7088 |
rs541509267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81670929 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGCAGATG | 7088 |
rs541533160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663723 | TGCCTCCCGGGTTCA[C/T]GCCATTCTCACGCCT | 7088 |
rs541537229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590636 | TAATAAGACTGTAAG[C/T]CCCCCAAAGGCAGCA | 7088 |
rs541550854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673397 | GGTAATGGGAAAATC[A/G]GTTCAGAGGTAGGAA | 7088 |
rs541611952 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662563 | ATTAGCAGGGCATGG[C/T]GATGCATGCCTGTAA | 7088 |
rs541642712 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612879 | CCTGGCCAACATGGT[A/G]AAACCCCGTCTCTAC | 7088 |
rs541653795 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81678807 | ATCGAGCCACTGCAC[A/T]CCAGCCTGGATGACA | 7088 |
rs541655031 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614223 | AGAAGACCCCTTTTC[A/C]AGTCTCCTTTTTAGG | 7088 |
rs541668352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632893 | AGAGGATGACTGGTT[C/T]AAGTAGAAATGGTAC | 7088 |
rs541690041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81600921 | CTCTCGATTATCAGT[A/G]CTACTGGTTCTCAGG | 7088 |
rs541725590 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | TLE1 | GRCh38.p7 | 9:81608058 | GGTGGTTTATTTGAA[A/T]CAAGGCTCTTATCAA | 7088 |
rs541740577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678382 | CCAGGCCCAATTAAT[G/T]TTTTTTAAATCTTTT | 7088 |
rs541766758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597359 | TGGGTCAGGGAATGC[A/G]GAAAGGGAGGAAGAC | 7088 |
rs541772468 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636493 | ACACAAGCAAGTGCA[A/G]CGGGTAATTAAGCAC | 7088 |
rs541775833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81667637 | CAATTTTGATATATG[G/T]ATCAAAGCCATTCCT | 7088 |
rs541840112 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684149 | CCTTCAGAGTAAATT[-/A]AAAAAAAAAAAAAAG | 7088 |
rs541840918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631340 | TCAGAAAGACACAGA[C/G]GTATAAAATACATCT | 7088 |
rs541841301 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81623441 | TATGAGGACACCATT[A/T]GCAAAAGAATGAAAC | 7088 |
rs541862453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620881 | TTATTCTTTCCCACT[A/G]CGACTTCCTGGTCAG | 7088 |
rs541901992 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690874 | GGTTCTTATGAAGTG[G/T]AACTTGAGTTAAAAG | 7088 |
rs541903228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629893 | AGTGCACTGATTACA[C/T]TTCTATTTCCTAGGC | 7088 |
rs541913066 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81673820 | TAATAATAAACCCAA[A/G]AAGCCGACTTCTGAA | 7088 |
rs541936602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81598704 | TTATACCAAATGTCA[A/C]TAAGAGATGGTAGCA | 7088 |
rs541974682 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595599 | CAAGGCGGGCGGATC[A/C]CGAGATCAGGAGATC | 7088 |
rs541995724 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669315 | TCTGTCTAATAGACA[G/T]GTGGATAAAAAGCCC | 7088 |
rs542021482 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665795 | TGGTTCTCCTTCCTG[-/C]CAATGATGGTCTTTT | 7088 |
rs542028282 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81648979 | TGTACACCTTTGCAC[A/T]ATAAATTATCCTTTT | 7088 |
rs542042648 | snp | C/G | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689431 | GGGTGGGGTGGCGCA[C/G]TCGGCTGCCTCCGGG | 7088 |
rs542049554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81612037 | GTCTGGCCTCATCAT[C/T]TGTTAGTGTCACTCA | 7088 |
rs542059733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605245 | GCCTCAGACCAGCCC[C/T]ACTCAACGTGTGGTC | 7088 |
rs542066783 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81636118 | GATGAGGTCAGAACA[C/G]GCAGCATTCATAGCA | 7088 |
rs542104200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81685529 | CTTGATGCAGAATAC[C/T]ACCATCAATCCACAG | 7088 |
rs542122836 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81611621 | GGTGAGTGTGTGGCT[G/T]GGAGACTGGGCGTCT | 7088 |
rs542125770 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685364 | CAACTGTAGAAGATA[C/T]CCAGCCCTTTCAAGA | 7088 |
rs542154221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648054 | AGGCGGGTGGATCAC[C/T]TAAGTTTGGGAGTTC | 7088 |
rs542187413 | snp | C/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687187 | AAGAACCAGGAAAGG[C/G]GGTAACTTGAATGAC | 7088 |
rs542196491 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629449 | TTTAAAACAGCCAAA[A/G]TAATTTTTTAAACCA | 7088 |
rs542200025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81640618 | ATGATACTGAAAACC[C/T]ACAAGGAATAAAGCG | 7088 |
rs542201642 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81617074 | GCACACCCTTATATC[-/A]AGAGTTTTTCCATAT | 7088 |
rs542236205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81633957 | TGACCTGTGTTTCAG[C/T]GGAAAGCTTTGCGAC | 7088 |
rs542255503 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81593772 | CTTTCTAAAAATACC[A/T]GTTTATGGTATGGAC | 7088 |
rs542263261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686062 | TTAATAGGGAAAAGG[A/G]ATAATGTGAACAATA | 7088 |
rs542272624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680692 | AATCTAGGCTCTAAA[C/T]GCAGAGAGCTTTCTC | 7088 |
rs542272878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674645 | CTTAAAGGTAAAGTA[C/T]AAGTCAAGTTTCATT | 7088 |
rs542285550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609170 | ACTCACTGCAACCTC[C/T]GCCACCCAGGTTCAA | 7088 |
rs542316781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599422 | ACATCGTGAGCAACA[C/T]AAGGCATGTCGACAT | 7088 |
rs542359459 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81644048 | AAAAACGGGAGATGC[A/G]GCCTCACACCCATTA | 7088 |
rs542366032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602334 | GAACATCCCTTATCC[A/G]AAATGCTTCAGGACC | 7088 |
rs542391412 | in-del | -/TCTAAGGTCTGAGGCCTCTGT | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81618905 | GTCTGTCATCAGTGA[-/TCTAAGGTCTGAGGCCTCTGT]TCCAGATTCTCCAAC | 7088 |
rs542420782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649645 | GGCCTCTCCCATTGT[C/T]CTTTACCCTAAGTCG | 7088 |
rs542467502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81620245 | AAAGGCAGGAAGTCT[A/G]AAGCTTAACACTGAG | 7088 |
rs542541146 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81678990 | TACCAAAAAATAATT[A/T]AAAAAAAATTAACCA | 7088 |
rs542554606 | snp | A/G | 1.65712e-05 | 0.00287843 | intron-variant | TLE1 | GRCh38.p7 | 9:81584542 | AGAATTAGCAAAGGA[A/G]TATCTAGTTTTCACA | 7088 |
rs542572781 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81655166 | GTCAGGAGTTCAAGA[C/G]CAGCCTAGCCAAGAT | 7088 |
rs542586409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81653715 | GCTTATGCTACTTAA[A/G]GCAAAAGCTGTACAT | 7088 |
rs542602556 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610081 | CTATTTATAGAAAGT[A/G]TTAACACTCCTCAGG | 7088 |
rs542653016 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81654592 | GTGATCCGCCCGCCT[-/C]GGCCTCCCAAAGTGC | 7088 |
rs542673773 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81677243 | ACTCGTCTTCCCCCC[C/G]CCAAAAAAAAGACCT | 7088 |
rs542689895 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81596488 | CAATAATAACAGAGC[G/T]TTTTCAATAAAAGGC | 7088 |
rs542695653 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688359 | AGCGGGGAGCGCGCT[A/G]GCCACGCACGCGCGC | 7088 |
rs542749793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653313 | TGCACACTTAGAACA[A/C]GTTACAGCATTTACT | 7088 |
rs542781481 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81633158 | AGACAAGAGCAGAGC[A/G]AACAGTCATATAAGA | 7088 |
rs542817849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645717 | TGCACTCCAGCCTGG[A/G]CAACAAGAGTGAAAC | 7088 |
rs542832794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628127 | GTAACTGCATTGAAT[C/G]TAATGAATGATGCAT | 7088 |
rs542894589 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666844 | AAATAAAGACAAAGG[C/T]CTGAAGCACTGGCTC | 7088 |
rs542941657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663649 | TTTTTTTGAGATGGA[G/T]TCTCGCTCTGTCACC | 7088 |
rs542956275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634398 | AGGGGAAAACAGACA[C/T]GACAGGAGGGGAAGG | 7088 |
rs542968818 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659601 | CTGAGGCAGGAGGAA[C/G]CAGGAGTCCAAATTA | 7088 |
rs542970354 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626245 | CTCGTGACACCTCAT[C/T]TATCCTCAGTTACAC | 7088 |
rs542992333 | in-del | -/GCGGCGGCT | 0.00140133 | 0.0264329 | cds-indel | TLE1 | GRCh38.p7 | 9:81611803 | GCCACCACGGCGGCC[-/GCGGCGGCT]GCGGCGCTCATCTGG | 7088 |
rs543009726 | in-del | -/T | 0.155987 | 0.23165 | intron-variant | TLE1 | GRCh38.p7 | 9:81663623 | CCGCACAGAATAGAC[-/T]TTTTTTTTTTTTTTT | 7088 |
rs543063073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81622146 | GCCCTCTGAAAAGCT[A/G]GGCCGGGGCAGCAGC | 7088 |
rs543069718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638159 | GCCTAATGGCAGTGA[C/T]GGGGGAGTTTACGCT | 7088 |
rs543089218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669134 | CAGAAAAGACTTCCT[A/G]CCATTTGGACTGTGA | 7088 |
rs543100902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615260 | TTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGTG | 7088 |
rs543104610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624706 | AAAGACTTTAAATGT[C/T]GGGCAGACTTCTATT | 7088 |
rs543105928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665574 | AGCAACACTAATTGC[C/T]CCCATTCTCTAGCTC | 7088 |
rs543152029 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684673 | ATGAAATAGCACATA[C/T]ACATCAAGTAAGAAT | 7088 |
rs543155959 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657570 | CCAGTCTGAATGAAA[A/T]GAACTTGTAAACCTT | 7088 |
rs543162801 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653834 | GTGTTGGATAGACTA[A/G]CAGGGGGTTTACACA | 7088 |
rs543177015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668398 | TAAGTATTTAGAAGA[C/G]AGTAAGCAAAAGGAT | 7088 |
rs543277009 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591226 | CTGTCTCCTTCAAAA[C/T]AGTAAACAAAACAAA | 7088 |
rs543293500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596955 | ATTCATTTACTTATT[C/G]AAGAGGAAGTCGAGG | 7088 |
rs543332881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677603 | AACAACTCAGGTAAA[C/T]GCACTCAAGCTTTTC | 7088 |
rs543354518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81637562 | TAATCTGACCTTCTA[C/G]GTCCCCTGAACAAAC | 7088 |
rs543374167 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588021 | AAACAGCACCTGCGA[C/T]TGTCTTTCCCTGTTT | 7088 |
rs543429960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619722 | CATACATCGGCTGCA[A/G]TGTTTATAACCCTGA | 7088 |
rs543432621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81618618 | CAAAACTAATACTAA[C/T]GAAAATCTGTTTTCT | 7088 |
rs543438770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612208 | CATTTGTGTAAATGG[C/T]AGCACCAGGAAGCCA | 7088 |
rs543496978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617918 | TAATCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG | 7088 |
rs543504067 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588442 | CCCAGAGACAAAGGG[-/T]CACGCATGCCGGCCT | 7088 |
rs543529784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589527 | TTACTCCCCAGGAGC[C/T]GGCACGGAGCAAGGG | 7088 |
rs543555602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676585 | ATGCAGGAAGAGAAA[A/G]AAGCAGTGGCCAAGA | 7088 |
rs543583865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81631297 | TGTCAAAAATACCAA[C/T]AGGAGGTTATCCGAC | 7088 |
rs543621880 | snp | A/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588400 | CTTTCTGTGTTAGAA[A/G]GAGCCCTGCATTAGG | 7088 |
rs543634046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681448 | CCAACTACTGAGGAG[G/T]CTGAGGCAGGAGAAT | 7088 |
rs543691753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680198 | CTGAAGCCAGGGAAC[A/G]TGTTCATGACTTGCC | 7088 |
rs543703202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81674542 | CATACACACAAAGTT[C/T]AAAATCAGAGTCCTT | 7088 |
rs543726514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599302 | CCCAGCTGCAAAAGT[C/G]GAGCTGTTAATCTTT | 7088 |
rs543756204 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584043 | GCTGATGGACTTGTC[A/G]CCTCCTCTTTGTAGA | 7088 |
rs543759136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592271 | GCTGAGGCAGGAGAA[C/T]GGCGTAAACCCCGGA | 7088 |
rs543760696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81593556 | TCTGTAAAGCATTCC[C/T]TCAAATCTCATTATA | 7088 |
rs543769930 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81607338 | ACTGACCCTGTTAAT[A/G]CACACACACACACAC | 7088 |
rs543780778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81625633 | AATGTAAGTAGGTGG[A/G]TTGACTGAACCTCAG | 7088 |
rs543786343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651156 | AAAGTGTCTGAGGGA[A/G]CTATAAAGACCAGCA | 7088 |
rs543800840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663010 | GCACCACCACGTGCA[A/G]CTAATTTTTGCATTT | 7088 |
rs543816200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586578 | AGGTTATATGGTGCA[C/T]GGCTGTGCTTATGGA | 7088 |
rs543842109 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642490 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 7088 |
rs543845258 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81628619 | GAAGAGTAACAAAAG[-/A]AAAGAAACCACTTTA | 7088 |
rs543859422 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662972 | CATGCCTCAGCCTCC[C/G]GAGTGGCTGGGACTA | 7088 |
rs543871378 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655870 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAACAA | 7088 |
rs543900617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669967 | CAATTCAGGTAAGTG[C/T]CACTGCCAAATTTTC | 7088 |
rs543987955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617617 | TGAGGCACAAGGATC[A/G]TTTGAACCCAGCAGG | 7088 |
rs543999760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673032 | AATCCCAGCACTTTG[A/G]GAGGCTGAGGGAGGC | 7088 |
rs544022525 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593329 | TTACAGAGGAAGCAA[C/T]CCCTATCTCGGCAAT | 7088 |
rs544034260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639065 | GTACATACTTAGCTG[C/G]GACTACAGGTGTGCA | 7088 |
rs544053643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688125 | GGGCGAGAAGGTCCG[A/C]CGGGCCTCAGAAGCC | 7088 |
rs544082845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81650098 | TGTTGCCAAGGCATC[C/T]AGAGCTAACCTGCCT | 7088 |
rs544096890 | in-del | -/A | 0.0185938 | 0.0946107 | intron-variant | TLE1 | GRCh38.p7 | 9:81655367 | TCCACCTCAAAAAAT[-/A]AAAAAAAATAAAGAA | 7088 |
rs544111061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603181 | ACCCTTCTGCAGGGA[A/T]TCCCTGCTTGACTAT | 7088 |
rs544113507 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81683199 | ATTAAAGCTCTCTGT[A/T]CGGAAAGTTTCCCCA | 7088 |
rs544115345 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688342 | CCGGAAAGCCAAGCA[C/G]AAGCGGGGAGCGCGC | 7088 |
rs544152989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609666 | TTTTTATAATTCTAG[A/G]TCTCTTGGAGCACTC | 7088 |
rs544155725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81644671 | AGCAATGTGAATACG[C/T]TAAAAACCACAGAAG | 7088 |
rs544164409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643301 | GAGTACAATGGTGCG[A/C]TCTCGGCTCACGGCA | 7088 |
rs544167300 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81653229 | GCAACAGGTGCCAAC[C/G]AGGATACCCAGTATT | 7088 |
rs544171200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81636077 | AAAGAGAGCATGGTT[C/T]TAATTAGAAGCAAAA | 7088 |
rs544197053 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650061 | TCGCTTGCATTGCGC[C/T]TGATTCACCACTTTG | 7088 |
rs544307969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81679774 | AGCAATGGGGAGGGG[A/G]GAGGGTAGGAAACGA | 7088 |
rs544317984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678767 | TCCCGGCTACTCAGG[A/G]AGGTAGAGGTTGCAG | 7088 |
rs544320149 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81647846 | AAATATTCCTATGTG[A/G]ATTACCAAAAACACC | 7088 |
rs544333993 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648499 | TACAATTATACATCA[A/G]CTGAAAAAAACAAAT | 7088 |
rs544399063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616541 | TAAGAAGTTGCAAGA[C/G]GTCCCCCCACCGAGG | 7088 |
rs544410474 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81622808 | ACCTTTGATGCTGTA[A/G]AACTGACTCAAAACA | 7088 |
rs544411636 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644686 | CTAAAAACCACAGAA[C/G]TGTATGCTTTAAAAA | 7088 |
rs544424293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81672178 | GGTACTGGCACAACT[C/T]GTCTGAACTGTGCCC | 7088 |
rs544425850 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81641979 | GTAAGCGGAGATCGC[A/G]CCATTGCACTCCAGC | 7088 |
rs544438847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617200 | GCAAACAAAACCCAA[A/T]CTTTTTCTCTTAAGT | 7088 |
rs544443700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603934 | TTGAACCCGGGAGGT[A/G]GAAGTTGCAGTGAGC | 7088 |
rs544495562 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688877 | GCAGCGGAGGCTCCT[A/G]GCCGGGGAGCGACGG | 7088 |
rs544513049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610949 | CACTTTGCCCGCCAC[C/T]GCACAGCCTCTCCTA | 7088 |
rs544521545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653659 | GAACAGCTTTCTATT[G/T]AAAAGATATAAAAGA | 7088 |
rs544547660 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | TLE1 | GRCh38.p7 | 9:81668705 | AATTAAAAGTATGCC[-/A]AAAAAAAAGGCCTTC | 7088 |
rs544573599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645675 | AACCCGGGAGGCAGA[A/G]GCTGTGGTGAGCTGA | 7088 |
rs544603125 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628927 | TCTGCAAAAGAGCAC[A/G]GACCCACCCAGTCCA | 7088 |
rs544610390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646141 | AATTTTTTTAAAAAA[A/G]GAAAGAAATATGTGG | 7088 |
rs544644638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686018 | CCATAAACTATCTAG[C/G]TAAACACCCAAAAGC | 7088 |
rs544666492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611577 | CTCACTTAATGAAGC[A/C]GCATGCTGATGAAAG | 7088 |
rs544701610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605085 | CTGACAGTTCACACT[C/G]AGTCTATGAATGGCA | 7088 |
rs544717919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81648761 | CCACAAATAAGATGT[C/T]ACAACATTTAATAAC | 7088 |
rs544741590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613740 | AGAGACACAGAACAT[C/G]ATCACACTTCTTCCT | 7088 |
rs544778195 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81608172 | CAAGCACTTTGGGAG[A/G]CCAAGGCAGGAGGAC | 7088 |
rs544792229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619554 | CTATCCTCTGTCTAG[C/T]GTTTAGACCTCCACA | 7088 |
rs544841236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620159 | GGGGGACTCCTAACA[A/C]GAGCAGGGCCCTGAG | 7088 |
rs544869383 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606604 | GACACAGGTGGGGAA[C/T]ATCACACACTGGGGC | 7088 |
rs544935458 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81660347 | GGCTGTTCACAAAAA[A/T]AAAAAAACAAAATCA | 7088 |
rs544968588 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589486 | AAAGATTTGTAAGAC[A/C/G]CTACCCCATTCTATC | 7088 |
rs544989878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639622 | CAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 7088 |
rs545005208 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687504 | AGCAGTAAGTCAGAG[A/G]AGGCAAGAACGGGTG | 7088 |
rs545027523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659212 | CGCGCCTGGCCTCTC[A/G]TAGTGACTCCTGCCC | 7088 |
rs545036266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682119 | GTTAGCCGGGCATGG[C/T]GGCGGACACCTGTAA | 7088 |
rs545041686 | in-del | -/AG | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81654364 | ATGTATTTTTGAGAC[-/AG]AGTCTTGCTCTGTCG | 7088 |
rs545062054 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81601590 | GGGAGAACAGCAGTG[C/T]TACAGTGCCAGAAAA | 7088 |
rs545076316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81664521 | TGTTTAAAATATAAT[C/T]ATGCCGATAAAATAA | 7088 |
rs545140077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657012 | GTCAATATTGAGTTT[C/T]GTTGACCTTCCTTTA | 7088 |
rs545209135 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603566 | AGGGATTTCCACAAA[C/T]AAACTTACCAAAATA | 7088 |
rs545230632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586619 | TGCTGCTAGAGTTTA[C/T]TTTAAAATAATCCAG | 7088 |
rs545232922 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691291 | CATTTTAGATAATAC[A/G]TTTCACTGTTGGAGT | 7088 |
rs545234170 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81671505 | CAAAAATTAGCAGGG[C/T]GTGGTGGCATGTGCC | 7088 |
rs545243195 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641725 | CAAATCAGAGCCACA[A/G]TGAAATATCACCTCA | 7088 |
rs545271438 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81603419 | TGAGAAATGAGAGAT[-/C]CAGGAAAGACTTTCT | 7088 |
rs545319209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669837 | CTGACTTTATACCAA[C/T]GGTCCCCCTTTGCTG | 7088 |
rs545333001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81640408 | AATTAAAAAAAAAAA[A/G]AAATCCTTGTATTTT | 7088 |
rs545336304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682534 | AAGATAACATGAGTG[A/G]GCTAAAATAAGGTTT | 7088 |
rs545351883 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583936 | GCTGTCATGTGAGTC[A/G]GCAGATTCCGTTCCT | 7088 |
rs545363187 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81646711 | GAGCCCTTTAGGTCT[-/A]ACAACTCAATCTCTT | 7088 |
rs545391044 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640420 | AAAAAAATCCTTGTA[A/T]TTTACAAAGCAATTT | 7088 |
rs545402049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81677098 | ACAATTAGCTGGGTC[C/T]GTGGTGGCACGTGCC | 7088 |
rs545408793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621616 | GGGGATACCTTTAAG[C/T]TAGACCACATCTAAT | 7088 |
rs545434733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81627990 | TTGGGAGACCAAGGT[G/T]GGAGAATCACTTGAA | 7088 |
rs545455953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615190 | ATGGTGGTACCAGGC[A/G]TGGTGGTGAGTGCCT | 7088 |
rs545470095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617455 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG | 7088 |
rs545481505 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81591816 | TTTTGAAGTTATTTG[G/T]TTTTTTTAAAAAATG | 7088 |
rs545499525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81658774 | AAATAGTCTGGATTG[C/T]AGCAGCATACAAACT | 7088 |
rs545525315 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661769 | AATCCCCCCCCCAAA[A/G]AAAATGTACACAGAA | 7088 |
rs545529473 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638356 | ATAAACACAAAGTGT[C/G]ATTTCTAAGATAACA | 7088 |
rs545577402 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681171 | AAATATCACATGGAG[C/T]TCTTTCCCTTTCCCA | 7088 |
rs545577411 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633375 | TCTGTCTGCTCCCGA[C/G]GTTACCAAGAAACGC | 7088 |
rs545591769 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610404 | AAAGCAACATAAATG[A/G]GAACAGTAACATGGC | 7088 |
rs545627684 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81635916 | TATAATCCCAACACT[C/T]TGGAGGCCAAGGCAG | 7088 |
rs545632194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81626908 | ATTTTTAAATAACCT[C/T]ATGACACTGCCGTTC | 7088 |
rs545637010 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684785 | GACTTATTGTACCAG[C/T]GTCTTGATGAAAAAG | 7088 |
rs545644881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676734 | AGACCCTGAAGACAA[C/T]TTACATCTGCTATCT | 7088 |
rs545693499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602269 | CGGAAAAGCAGGCTG[A/G]GGGGATATTACCAGC | 7088 |
rs545701766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589982 | GTCATGATGACTTCT[A/G]GAGCCCGTCCCTTCT | 7088 |
rs545738591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661541 | TGGATCATAAAAAAA[C/T]GGTGCTTATGCTGAG | 7088 |
rs545741127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81678951 | TTTGAGACCAGCCTG[A/G]ACAACATGCAGAAAC | 7088 |
rs545756552 | snp | A/G | | | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593199 | ATGCCGGGGGATTCC[A/G]GGTCCGATGAGGGCG | 7088 |
rs545798320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592307 | AGCCTGCAGTGAGCC[A/G]AGATCCGGCCACTGC | 7088 |
rs545807161 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81624909 | ACTGTTCAAAACAAA[C/T]TGAAATTCTAAAACC | 7088 |
rs545855719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638983 | GGCTGGAGTGCAGCA[C/G]TGCAATCATGGCTCA | 7088 |
rs545867271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599943 | AACTTCTTAAAATGG[A/G]TATGTAAAAGAAGAT | 7088 |
rs545871837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587997 | TAACCTTCCCCTGAG[A/G]AGGAGGGGAAACAGC | 7088 |
rs545876800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81623521 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTA | 7088 |
rs545892422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632126 | TAGGAACCCTGGAAT[C/G]GCAAAACAATAAGGC | 7088 |
rs545969816 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690378 | TGCGTAAATGAGCAA[C/T]GCCACGGTTGGCGTA | 7088 |
rs545992047 | in-del | -/T | 0.0151355 | 0.0856661 | intron-variant | TLE1 | GRCh38.p7 | 9:81633588 | ATACACAAAGCCTAT[-/T]TTTTTTATTTCTTGA | 7088 |
rs546005068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681334 | GCGGGGGGAATCACT[C/T]GAGGTCAGGAGTTCG | 7088 |
rs546027141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599466 | GTGGGGGCTGGGGGA[A/G]CCGGGCTCCTTATGG | 7088 |
rs546028757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81606778 | CTTAAAGTATAATTA[A/T]AAAAAAAACCATATA | 7088 |
rs546034770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81685198 | CTGACTATTGCTTCA[C/T]GCAGCCCCAAAGCAT | 7088 |
rs546044125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81630654 | TGGCCTGTAGCAACC[A/G]CCCTTAACCTTTCAC | 7088 |
rs546066750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686120 | CTTGGTGCCTATCTG[A/G]TTAGATGACAAGAAT | 7088 |
rs546095089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597707 | GTCAGAATCGAAAAG[A/T]ATAAAGCCCACTCGA | 7088 |
rs546124362 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683666 | GTTAAGGGTCTGTCA[C/G]CATTTCCAATATCAA | 7088 |
rs546132994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588903 | AGAGCTCCAAACTTT[C/T]AACCTGAGCTTGGAT | 7088 |
rs546137361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81598352 | CCCTCCCAAGTACAC[A/G]CCGCTTCCTCCCTCC | 7088 |
rs546174871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81627426 | TATCCACCTGACTTA[C/T]TGCATCCACAGTAAA | 7088 |
rs546198807 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655728 | AAAAGCACGCAGTCC[A/G]TGACCTTGAGAAATA | 7088 |
rs546202398 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668874 | GGGGCCACCAGAAGT[C/T]ACCACTCCTGTAATT | 7088 |
rs546240681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680769 | AGGACCACTCCAATC[C/T]TGATGACAGCTACCC | 7088 |
rs546301591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621385 | ATGTTACAATGAGTT[A/C]TTTTAAGTGTGGGAT | 7088 |
rs546319956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664794 | AAACTCCAGCGTACA[C/T]GAGGATGGTCTTGTG | 7088 |
rs546337164 | snp | C/G | 0.00101959 | 0.0225556 | intron-variant | TLE1 | GRCh38.p7 | 9:81634053 | TTTGCAGCACTGTAA[C/G]AGTATGAGGACAAAG | 7088 |
rs546354371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590164 | TTTGAGAACAGCTCT[A/G]GTGTGAGCACTGACT | 7088 |
rs546361334 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597176 | GGTCGCAGGGGTTGC[C/T]GTAAGGATTAAAGTG | 7088 |
rs546371818 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623388 | AATTTCGAATGCTAT[-/G]TTGTCTGGGTCCCAT | 7088 |
rs546381274 | snp | C/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690259 | TTGTTTGATGCTACT[C/T]TAAAAGTGAGGCCAC | 7088 |
rs546403149 | snp | C/G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595634 | CCATCCTGGCTAACA[C/G/T]AGTGAAACCCCATCT | 7088 |
rs546426350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686502 | ACAAAAGGTCAATAA[C/T]GAGAAAGCCCCTGAC | 7088 |
rs546460723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682164 | GAGGCTGAGGCAGGA[C/G]AATTGCTTGAACCCA | 7088 |
rs546467394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655666 | CTTACTAAATGCCAC[C/T]TATATTACTGAATTA | 7088 |
rs546494672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81601867 | CACAATCCTGGACCT[A/G]TCTCCCACCTATTCA | 7088 |
rs546512644 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81617517 | GACCAGCCTGGCCAA[C/T]GTGGTGAAACCCTGT | 7088 |
rs546539352 | in-del | -/TAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684393 | CAATTACATTATTAA[-/TAA]AAGGCCCTGAAAATC | 7088 |
rs546550229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649677 | CCCCTGAACAATACT[A/G]ACAGCTGCTATCAAA | 7088 |
rs546642726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634843 | CTACACCCTTGCATT[C/G]ACTTACCACAGTAGT | 7088 |
rs546655588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596534 | TCATGACCATGGTGA[A/G]GGGATCCCAGAAGGA | 7088 |
rs546676912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677291 | ACAACTCAGGCCGGG[C/T]GCAGTGGCTCACACC | 7088 |
rs546676983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671203 | ATGAATACAGATTTA[A/C]CAACCAGTTCAAAAC | 7088 |
rs546677417 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611684 | TGCCCACGCAGCGCA[C/G]AGAGGCCTGGCCCCA | 7088 |
rs546680558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647140 | CAAATTTTCTTGCAC[C/T]CAACTGTCAGCTCTG | 7088 |
rs546685048 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | TLE1 | GRCh38.p7 | 9:81674478 | GGTCCTTACCCCCTT[-/A]CCACCCAAGGTCCCT | 7088 |
rs546732196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81584868 | AGATTCCCATCTTTA[A/G]TGGGAATTAAAGGAT | 7088 |
rs546737975 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81671639 | GACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 7088 |
rs546740494 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624148 | ACTTAACATTCTAAT[A/G]TGACATAATACCTGA | 7088 |
rs546742524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653452 | GTTAAGATTAAACCT[C/G]TATGACTTTGTAACT | 7088 |
rs546751454 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648981 | TACACCTTTGCACTA[C/T]AAATTATCCTTTTCA | 7088 |
rs546752918 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683512 | GCCAGACGTCACCAG[A/T]TTTAATAAGAATTAT | 7088 |
rs546779681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597110 | CCAGCCTGCAGTCTA[G/T]AATGTGTCTGTTTCG | 7088 |
rs546806097 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81641639 | CTGAACAGACATTTC[C/T]CAAAGAAGACACACA | 7088 |
rs546814750 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627076 | GAAATGGCCCTGAAA[C/T]TAAAAAGCCATTAGG | 7088 |
rs546842472 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TLE1 | GRCh38.p7 | 9:81627318 | AAAATTGTTCTCTCA[C/T]TTTTTTTTTTTTAAG | 7088 |
rs546846672 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81681908 | AGGCACTAGGGAGAC[A/G]TGGTCCACCTCATCT | 7088 |
rs546864824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645377 | TCTCCAAAAAAAAAA[A/T]AATAATAGTAATAAT | 7088 |
rs546883814 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667724 | ATTCCTGCTCCCCCC[C/G]AAGCTGAGTGGCTGG | 7088 |
rs546889909 | snp | A/C/G | 2.15915e-05 | 0.00328562 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688249 | GGAACATCGCTCTGG[A/C/G]GGCGGCCGGGGCTCT | 7088 |
rs546901668 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81639500 | TTAGGAAATTTGCTT[A/G]AAAGTCAAAATGCTT | 7088 |
rs546907661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81652063 | ACATCCCAAGTCTCT[C/T]CCTCTCCTCCTCCCA | 7088 |
rs546928901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614862 | AGGATCAGTCTACCA[C/G]GTAAATGACCAGCCT | 7088 |
rs546938501 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81642139 | AACCTTTGTACACTG[A/T]TCTTAGGAATGTAAA | 7088 |
rs547009634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597402 | TCAGGAAAGCACAAG[C/G]GCAGTGATGAGGCAA | 7088 |
rs547034082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680965 | ACACTAAGGTAAAAT[C/T]TGCAAAAGAGTAAAA | 7088 |
rs547036255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81674873 | TAAAATGTACATGGA[C/T]GCCAGGTGTGGTGGC | 7088 |
rs547049320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644750 | TGTAATCCCAGCACT[A/T]TGGGAGGCAGAGACA | 7088 |
rs547078992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603507 | TCCCTGTACCAGAAA[C/T]AGAAGAACAGCCTTA | 7088 |
rs547085283 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688410 | CTCGGCGCCCGCAGC[G/T]GCTCCGGCTCCCGCT | 7088 |
rs547109117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81603808 | TGAATTCAAGACCAG[C/T]CTGGCCAACATGGTG | 7088 |
rs547120883 | snp | C/T | 0.000225632 | 0.0106191 | intron-variant | TLE1 | GRCh38.p7 | 9:81600122 | AACAAGGCTCCTAAA[C/T]AGGACAAAGATACAA | 7088 |
rs547154252 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81684883 | ACTCAATCGAGGGTC[C/G]TTTGGGCTGAGCAAT | 7088 |
rs547155782 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677393 | ACATGATGAAATCCT[A/G]TCTCTACTAAAAATA | 7088 |
rs547160578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615303 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGTGAG | 7088 |
rs547215512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81654593 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 7088 |
rs547251854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665095 | AGAGGAGAGGTCAGG[A/C]CTGTCTCTCTCCAGA | 7088 |
rs547274263 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689670 | GGGGGGTGGGGGGGG[A/G]GCAGAAGGCCCGCAT | 7088 |
rs547297205 | snp | A/G | 2.15065e-05 | 0.00327915 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688247 | CGGGAACATCGCTCT[A/G]GCGGCGGCCGGGGCT | 7088 |
rs547412283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81594300 | GCCCATCAATGACAG[A/G]ATGGATAAAGAAAAT | 7088 |
rs547425266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631579 | CTCGAATTGCAGATG[C/T]GTGTCCCATAATGCC | 7088 |
rs547492638 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596296 | ACTCATCCGTCCCAC[A/G]GGAAGCCCATATGGA | 7088 |
rs547536068 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675178 | GGAAGATATATGACA[A/G]ATAGATATTACAAAA | 7088 |
rs547537719 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583636 | AACCCACATTGATGA[C/T]CCCAAAGCTTTAATA | 7088 |
rs547554093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663093 | TCAAATTATCCACAC[A/G]CCTCGGCCCCCCAAA | 7088 |
rs547582215 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690032 | CTAGAGAGCGCGCGG[C/G]CGCGCGCTAGCGGGA | 7088 |
rs547621668 | in-del | -/GACC | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81664898 | AACAAGTTCCCAGGT[-/GACC]GACCCTGAGGCTCTT | 7088 |
rs547629851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617545 | TGTCTCTACTAAAAA[C/T]ACAAAAATTAGCCGG | 7088 |
rs547640725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612252 | TATTCCCTACCCAAT[C/T]TACAGAGGGCAAACC | 7088 |
rs547641344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675560 | CATATTACTACAATA[A/G]AACTCCTCACTAAGA | 7088 |
rs547642180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605484 | TAAATAGTTTGAGCA[C/G]CACTGCCTCAGGCAA | 7088 |
rs547699879 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589302 | TGGCAGCTGCTCCCC[C/G]ATCCCTCTGCCCTCT | 7088 |
rs547706850 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81670183 | CTGAGTAATAGACTT[A/G]GAAAAGTAGCCACAT | 7088 |
rs547753477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81595090 | ATAAGCACGTATAAT[A/G]GGAACCATGGAGACT | 7088 |
rs547781403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687195 | GGAAAGGGGGTAACT[G/T]GAATGACAGGTCTTA | 7088 |
rs547810454 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81610693 | GTTGCAGGATGCTGA[A/G]TATCATTCCTGGCCC | 7088 |
rs547821694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613035 | TGCATTCCAGCCTGG[A/G]GGGGACAAGAGCAAG | 7088 |
rs547836177 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81615470 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCAAAGAG | 7088 |
rs547866939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586634 | TTTTAAAATAATCCA[G/T]TGTCTGGGGGTGGGA | 7088 |
rs547870065 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681511 | GCCGAGACTGTGCCA[C/T]CACACTCCAGCCTGG | 7088 |
rs547887925 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688562 | CCCCCGGCCTCAGCT[C/G]CCCGGGCGGGGAGGC | 7088 |
rs547893122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81656482 | CTCATACACATGCAC[A/G]CAGATACATATACAG | 7088 |
rs547932506 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638582 | TGATACTGATACTAC[C/T]ATATAGCCAAAACCC | 7088 |
rs547934289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613875 | AACACATGTCCTGGC[C/T]GCCAAGTCCAAGGAA | 7088 |
rs547995750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81625007 | GGGAGAAGCATATCT[A/G]AGAAGTCTAAAAGAA | 7088 |
rs548006603 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594331 | TGGCACATATACACC[-/A]ATGGAATACTATGCA | 7088 |
rs548029963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586245 | GATGGTCTCGATCTC[C/T]TGACTTTGTGATCCA | 7088 |
rs548063990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628413 | GTTCCCATAGGCCTC[A/C]GGGAATGAACGTGAT | 7088 |
rs548135458 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610677 | AGGGGCCGTCCTGGG[C/T]GTTGCAGGATGCTGA | 7088 |
rs548167258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81654160 | GTGTATAAAATGGTT[C/T]CCCCAGGTTATGTTA | 7088 |
rs548169907 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656814 | GTTTCATTTAATTTT[A/G]CACAATTAACAACTC | 7088 |
rs548180119 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81635069 | TGCTGAAACTCTATC[A/C]CTAGGCAAGAGGGGA | 7088 |
rs548190067 | in-del | -/AC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660935 | CCCCATCCCTACTAA[-/AC]ACACACACACACACA | 7088 |
rs548250729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81666124 | TGGAGTTCAGAAAGA[A/G]CCTGTTCACAGGAAA | 7088 |
rs548273972 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81623023 | TCTTCCAGCCCTGAC[C/G]CTGCTTTCATTGTTG | 7088 |
rs548288252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659613 | GAAGCAGGAGTCCAA[A/C]TTACCTGTCTACAAC | 7088 |
rs548323272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630261 | ATTCTCTTCCTAAAC[A/G]TCAACTAAATACCAC | 7088 |
rs548324084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659910 | AGAGATCTTCCCAAT[C/G]CCTCAAGGCCTGCCT | 7088 |
rs548325207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81637156 | TGAGGTCAGGAGTTT[A/G]AGACCAGCCTGACCA | 7088 |
rs548374049 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641740 | ATGAAATATCACCTC[A/C]GGCTGGGCGCAGTGG | 7088 |
rs548386744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81636485 | TGATGCATACACAAG[C/T]AAGTGCAGCGGGTAA | 7088 |
rs548412802 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81667170 | ACAATTCCAGCATTT[C/T]GGGAGGCCGAGGCAG | 7088 |
rs548462280 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81664652 | AGGATACCTTGAGCC[C/G]AGGAGTTTGAAACCA | 7088 |
rs548474202 | snp | C/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687943 | CGGGGAAGGTAGAGG[C/G]GATATGGCTGCAGGA | 7088 |
rs548548616 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81634698 | ATGAGATCCAGCATG[G/T]CACTCAATCTAAGAT | 7088 |
rs548554208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81633092 | AGTAATCACAGCAAA[C/T]AGTTTTGCCTCCAAA | 7088 |
rs548566977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604313 | GGAAAGGAAGTGACA[C/G]GATCTGGATCTTAGT | 7088 |
rs548605776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597514 | GAGTAGAGATGGACG[C/T]TTGGATAGAATCGTG | 7088 |
rs548617565 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623648 | AAAAAAAAAATTAGC[C/T]GGGTGGTGGTAGACA | 7088 |
rs548637207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81642353 | TGCTCAATCTGTACA[C/T]GATCCAGCAATCCCA | 7088 |
rs548643892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81666958 | CCTCATTTCTACAGA[A/C]AAAATTTAAAAATTA | 7088 |
rs548660517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673622 | GGTGCTACTGTCATC[C/T]CCTAATCCCACTCAC | 7088 |
rs548660597 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81679792 | GGGTAGGAAACGAAA[C/T]CAATCAAAGCTTTGA | 7088 |
rs548668510 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646649 | AAAGGAGAAAAATAA[C/T]CCAACATTTTACTAA | 7088 |
rs548707021 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643151 | TCTGGATTTCCAAGG[C/T]ACAACACGGTGACTA | 7088 |
rs548714364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639742 | GTGAGCACCACCACA[C/G]CCAGCTAATTTTTGT | 7088 |
rs548715268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587608 | CCTAGGGTAAAGGAG[A/G]GAGGGTTGTGAGGAG | 7088 |
rs548719147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674181 | TGCCATTGCCCTTGC[A/C]AACTGCTAAACAAGC | 7088 |
rs548741349 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618980 | CCATCTATCCAACCA[C/G]ACAAACCTAGTACAT | 7088 |
rs548773510 | in-del | -/G | 0.00239425 | 0.0345166 | intron-variant | TLE1 | GRCh38.p7 | 9:81628777 | ACTAAGTATGTGACC[-/G]GATGCACCCAGCCTC | 7088 |
rs548795090 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81622242 | TCCTCCTCCAGACTC[-/TG]TGCAGCATCCACGGC | 7088 |
rs548805850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597826 | CTAAAAGCAAAGAGT[C/G]CCCACCGGGCTCCTT | 7088 |
rs548820808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676758 | GCTATCTTAAAGATG[C/T]TCCCTTTCCAGGGCT | 7088 |
rs548822994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81613280 | CCCTACGTACATTTC[A/G]TATTTGTAGGGCAAT | 7088 |
rs548870811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684397 | TACATTATTAATAAA[A/G]GGCCCTGAAAATCAC | 7088 |
rs548895961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648258 | AGCCTGGGTTACAGA[C/G]TAACACTGTCTCCAA | 7088 |
rs548960974 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627383 | GCAATAAAACCTGAA[C/T]GTTAATCCAGTCCCA | 7088 |
rs548999898 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81661711 | GATAACCTCTAAATC[C/T]CTTCTGACTAGAAGT | 7088 |
rs549007809 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81677416 | TAAAAATACGAAAAA[G/T]TAGCCGGGCATCGTG | 7088 |
rs549010195 | snp | C/G | 0.000501899 | 0.0158334 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81584237 | AGCCTTCTTGTCCCC[C/G]GAGCCAGTGACTATG | 7088 |
rs549018539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676128 | TTGTGTGTAAAAACA[C/T]GTACAAACTTTTCTT | 7088 |
rs549047973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81590058 | AACTGCACCATCCGC[A/T]GGGACGGCTTCCCAG | 7088 |
rs549056033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682140 | ACACCTGTAATCCCA[A/G]CTACTCCGGAGGCTG | 7088 |
rs549070404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81595646 | ACAGAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 7088 |
rs549080058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81670418 | GCAACCTCCGCCTCC[C/T]GGGCTCAAGTGATTC | 7088 |
rs549084939 | in-del | -/AAAAAAAAAAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615107 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]AAAGAAGAAGAAGAA | 7088 |
rs549103227 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670421 | ACCTCCGCCTCCCGG[C/G]CTCAAGTGATTCTTC | 7088 |
rs549121967 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603916 | CTGAGGCAGGAGAAT[A/C]GCTTGAACCCGGGAG | 7088 |
rs549124292 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | TLE1 | GRCh38.p7 | 9:81658914 | TTTATTTATCTATTT[A/T]TTTATTTTTTTTTTA | 7088 |
rs549149400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596670 | ATTCAGAATGAAGCC[A/C]GATACAAAATAATGG | 7088 |
rs549155988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81600299 | ATATCCCATAAACCA[A/G]AAGTCATTTCTGACA | 7088 |
rs549181414 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605252 | ACCAGCCCTACTCAA[C/T]GTGTGGTCAGCAAAC | 7088 |
rs549181673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687997 | GCCCCTGTCCGCTCG[A/G]TATAGACGTCAAGTA | 7088 |
rs549204423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652756 | GACCAGCATGGGCAA[C/T]ATGGCAGAACCCTGT | 7088 |
rs549214508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602657 | TTTTCGAATTAAGAT[A/G]CTCAATCTGTATTCA | 7088 |
rs549238642 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668989 | ATGTGGGTTCCAGGA[C/T]ATGTCAATTCTCGTT | 7088 |
rs549241393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646414 | ACTAAATACAAGTTA[A/G]TAGAGCTAGAAGATC | 7088 |
rs549248878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81663816 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTC | 7088 |
rs549258175 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81650718 | ATACTGAAGGAGGGG[A/G]AAGGCAGTGCCTGGA | 7088 |
rs549287694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81658117 | GGGTTTCACCATGTA[C/G]AACAGGCTGATTTTA | 7088 |
rs549287746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664566 | GGGAAATCCAAATTT[A/T]AAAAATGTGGGGAGG | 7088 |
rs549325994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599700 | CCCATGACATCTACA[A/G]AATTTTTCCAGTTTG | 7088 |
rs549337696 | snp | C/G | 1.965e-05 | 0.00313443 | synonymous-codon, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688223 | GCGCCTCACCGGGTG[C/G]CGGCTCTGCGGGAAC | 7088 |
rs549369758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620687 | CCATTTAATTCATCT[C/T]ATCTAAAGACTTTGA | 7088 |
rs549372980 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81640994 | CAGACTTAACCCAAC[C/G]CAAACTAAAACCATG | 7088 |
rs549384077 | in-del | -/A/AA/AAA | 0.433236 | 0.170072 | intron-variant | TLE1 | GRCh38.p7 | 9:81648271 | AGTAACACTGTCTCC[-/A/AA/AAA]AAAAAAAAAAAAAAC | 7088 |
rs549391082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603415 | CACTTGAGAAATGAG[A/G]GATCCAGGAAAGACT | 7088 |
rs549398635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81584755 | ACTGGATACAGGACT[A/G]GTAGCATCATATCCA | 7088 |
rs549409600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680042 | TTTGGGAGAACATCT[C/T]AAGTCCTCTGGCGAA | 7088 |
rs549409617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686171 | TCTAACTGATTCCTC[C/T]TCATGGTCATCTGCT | 7088 |
rs549453420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651481 | GGAGAGCAGAACCCC[A/G]GTGAAAAGCCAGGGA | 7088 |
rs549526380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661071 | GGCAGAGGTTGCAGT[A/G]AGCTGAGATGGCGCC | 7088 |
rs549545114 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81606098 | GCCAGTTAGAATGGC[C/G]ATCATTAAAAAGTCA | 7088 |
rs549583568 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626551 | TGTCCACTGGCAACC[A/G]TATCATATCTCAGAA | 7088 |
rs549590857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81614130 | AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT | 7088 |
rs549620274 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623500 | AAATGGTCATGAGGC[C/T]GGGCACAGTGGCTCA | 7088 |
rs549629294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81608913 | CTGCACTCCAGCCTC[A/G]GCAACGAGTGAAACT | 7088 |
rs549629501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614832 | GGGCATGCTCTATGA[C/T]ATGCCCCGATATTAA | 7088 |
rs549630272 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649173 | TACCTAAGAAGCTTA[-/T]TTTTCTTAAATACCG | 7088 |
rs549651687 | snp | A/G | | | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634101 | CGGCCTCTCACCTCT[A/G]TGGTGCTCTGCATCG | 7088 |
rs549660347 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690230 | AGCAAATGTGTTTTT[C/T]AGTGCTGGACCCCTT | 7088 |
rs549665462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81667805 | GAACCTGGAATTATG[C/T]TTTTAATCAATATCA | 7088 |
rs549669792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655033 | CAGCTGAACATAATA[A/C]AAGGTGTCCTTAGTG | 7088 |
rs549687623 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81660566 | CTACAGGTGCCTGCT[A/C]CCACACCCGGCTAAT | 7088 |
rs549688406 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81623589 | TTCGAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 7088 |
rs549693605 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627404 | CCAGTCCCACCAAGG[-/C]CCCCGATATCCACCT | 7088 |
rs549729551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611329 | TGTAACATAGGCATA[C/G]AAAGAGAAAGCGATG | 7088 |
rs549742434 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658507 | TGCCAGGTCTCTAAA[A/C]CCTAATCTTAAACTA | 7088 |
rs549811772 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689639 | GAGCCGGCGGGGGAC[A/G]TGAGCCCGGGAGGTT | 7088 |
rs549819261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618179 | TATGGAAAAAGCAGG[A/G]CATCTCAATGGTTTT | 7088 |
rs549861437 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81611676 | GCTGCTCCTGCCCAC[A/G]CAGCGCAGAGAGGCC | 7088 |
rs549928077 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638686 | CTGGAATACAGTGGC[A/G]CAATCTTGGCTCACT | 7088 |
rs549997328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81669420 | GAGGGGAAATAACCT[C/T]CTAAGCCACAGACTA | 7088 |
rs550010802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588619 | TCAGCCAACAGGGAT[A/C]TGCTGAGCACAGATG | 7088 |
rs550026184 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583556 | GAGCCTACCACCAAA[A/T]ATATTTATAAAATAA | 7088 |
rs550048684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624976 | TGGGTACAGGGTCAA[C/G]TACCCTGTACATAAA | 7088 |
rs550067985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81593999 | CAATGAGGTGTAAGA[A/G]GAAGCTGTTGGATGG | 7088 |
rs550142407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622908 | AGCTGCCGGACGCCC[A/G]GCAGGCTTTCCACCT | 7088 |
rs550159063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656423 | TTCTCGGAAATTCAC[A/C]TTGAAGGTTTCCAGT | 7088 |
rs550269558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659471 | GCAACAACAATAAAT[C/T]TGCATTCAAGAGCTA | 7088 |
rs550284944 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684481 | ACATTATGAAATCTA[C/T]GATGAATTAAAAATC | 7088 |
rs550344234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81658817 | TAGTATTATCTCTTG[C/T]TTCAACAAAAGGGTA | 7088 |
rs550346400 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685441 | ATCTGTCAATAAAGA[A/G]GCTAGTTTATATTTC | 7088 |
rs550378199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668840 | GAAGATAATGGAAAC[A/G]AGAACAATTTATAAA | 7088 |
rs550412372 | in-del | -/A | 0.0603597 | 0.1629 | intron-variant | TLE1 | GRCh38.p7 | 9:81680929 | AAAACACACAGGGTT[-/A]AAAAAAAAAAAACAA | 7088 |
rs550433727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602563 | ACCTTGTCACATGAG[A/G]TCAGGTGTGGAATTT | 7088 |
rs550433968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81596155 | CTGTCTGCTGATCTT[C/T]GGAAGACACCCACTT | 7088 |
rs550438574 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81648817 | AGAAATTTTAAAAAA[-/C]AAACAAAAATGTTGC | 7088 |
rs550472940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81596641 | GAGCATTCATGAATA[C/T]CGCTCACACCTGAAT | 7088 |
rs550526563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81636303 | TTGCAGTGGCATCAC[A/G]GTCCACTAGGCATGC | 7088 |
rs550541638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81637793 | GTTTCTGCAGGGCAG[C/T]GCTCCTAGATAATAT | 7088 |
rs550553623 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682779 | CTCTACTGTATAGAG[A/C/G]TATCTAGAGTTTACC | 7088 |
rs550576301 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603894 | GTAATCCCAGCGACT[C/T]GGGAGGCTGAGGCAG | 7088 |
rs550612912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81677330 | CAGCACTTTGGGAGG[C/T]TGAGGTGGGCAGATC | 7088 |
rs550672225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586078 | GCTGGAGTGAAGCGG[C/T]GTTATCTCGGCTCAC | 7088 |
rs550683047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81664820 | TTGTGCTTGTTAATA[C/T]ACAGATGACTAGGCC | 7088 |
rs550683336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672428 | AACCTCCGCCTCCCA[A/G]GTTCAAGTGATTGTC | 7088 |
rs550692389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628343 | GCCAGAATTCCACTA[A/C]AGTCTGCCTTTGTAC | 7088 |
rs550705921 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602999 | TGGGAAACCCATCTT[A/G]TCATCTTAACACCGG | 7088 |
rs550711576 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682882 | ATGAAAGACTTAAGT[A/G]TCTATTACCATTCCT | 7088 |
rs550714493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647785 | AGTATCCTCCCCAAG[C/T]CCATCTGATCCCAAG | 7088 |
rs550719565 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81665254 | TTCCACCCATGGCAA[C/T]GTAATCTCGCCCCTT | 7088 |
rs550745791 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618700 | GGTGGTGAAAAAATA[C/T]AAACTAAAAGAGTTT | 7088 |
rs550755879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634661 | AAACATGAGCTAGTT[C/G]TGTCTTTATGCGCCT | 7088 |
rs550805519 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602177 | GCTGCTCCAGGGAGC[A/G]GGGGCTGGAGTCATC | 7088 |
rs550824453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81635502 | GTATCCAAGAAATGG[C/T]CCCTGTACCATGAAT | 7088 |
rs550886501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81640066 | AAAAGAATGCTACTG[C/G]TGCATCTAATGGGTG | 7088 |
rs550889682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603715 | TTTGTATAAAAGTGA[C/T]ACAAGGTCAGGCGTG | 7088 |
rs550896486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81647201 | GACGGGAGGACAGTC[C/T]CCACTGGTCATCTGA | 7088 |
rs550906653 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667022 | TACTGGGGATGCTTA[C/G]GCAAAGGATCACTTG | 7088 |
rs550914417 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81621836 | GAAGGCAATCCCAAG[C/T]CTCTTGGCCCGCCTC | 7088 |
rs550923556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81640812 | CTTATCACCATGTTG[C/T]TGTAGCCTCTAACAA | 7088 |
rs550951102 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81610104 | TCCTCAGGAAAAGAC[A/G]CCAGAAATCTCCTTG | 7088 |
rs550988271 | in-del | -/TG | 0.147321 | 0.227941 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689661 | CGGGAGGTTGGGGGG[-/TG]GGGGGGGGGCAGAAG | 7088 |
rs551028240 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663457 | TGCCTGCAAAGCAAC[A/G]CAGCTGCTGAAAGGC | 7088 |
rs551049631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644787 | TCACCTGAGGTCAGG[A/T]GTTTGAGAACAGCCT | 7088 |
rs551075595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681532 | TCCAGCCTGGGTGAC[A/G]GAACGAGATTCCGTC | 7088 |
rs551091839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632323 | CTCCTCCACGCACAT[A/C]CAGATACATGAAATA | 7088 |
rs551101391 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81592182 | GCTAACATGGTGAAA[C/G]CCCGTCTCTACTAAA | 7088 |
rs551196935 | in-del | -/CTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613906 | GACCCCTTTTCTTTT[-/CTT]TTTTTTTTTTTTTTT | 7088 |
rs551225663 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81681320 | TTGCGAAGCCGAGGC[-/G]GGGGGGAATCACTTG | 7088 |
rs551234417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684214 | TCACTTAAATGACGA[C/T]AGATGTTAGCCACAG | 7088 |
rs551265023 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688308 | ATTTCCAACTTTAAT[C/T]CCGCCGAGGAAAATT | 7088 |
rs551270516 | snp | A/C | 1.65784e-05 | 0.00287905 | intron-variant | TLE1 | GRCh38.p7 | 9:81654056 | AAAGACAAAGCCACA[A/C]AAATGTTTAGAATAC | 7088 |
rs551275008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649776 | CTCTGGGGAGACAGG[C/T]TGACACACTGCATGT | 7088 |
rs551286290 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612846 | GCAGATCACCTGAGG[A/T]CAGGAGTTTGAGACC | 7088 |
rs551338336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687653 | AAGCTCTTCCCAGTC[C/T]CCAGGGCGGATTGCG | 7088 |
rs551345268 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600464 | CCCTGGAGATCCCCA[A/T]CTCATTTTTCTTTTT | 7088 |
rs551353097 | snp | A/G | | | splice-donor-variant, intron-variant | TLE1 | GRCh38.p7 | 9:81652182 | AAGCTGGTTATACAC[A/G]CTGTAGGAGGTAGAC | 7088 |
rs551397809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81601937 | GGACAAGACTTCGGG[A/C]ACTTCCATCCTCCTG | 7088 |
rs551400796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656391 | CACACATTCCTGCAA[C/T]ACTCTGTACATTCCT | 7088 |
rs551403035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589386 | TCAGAACGTGCTGGG[C/T]TACAGTGGATACAAA | 7088 |
rs551409172 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681108 | CACATCAAAACTGTA[A/C]AAGCAGTTTCACTCC | 7088 |
rs551468354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675718 | TTTTTGTTTTTTTTT[C/T]TGAGACGGAGTCTCG | 7088 |
rs551473323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687144 | AAACAATGGGAGGAG[A/G]AGGAGACAAGAGAAG | 7088 |
rs551475124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81600247 | ACTACAGACAAAAAC[A/G]AGCATTATCCAAGCA | 7088 |
rs551511809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81595146 | AAAACAATATAGCTC[A/C]AAGCCCTCACATCAC | 7088 |
rs551544808 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674811 | CAAAAGTACAAAGGG[C/G]AAGTCTAGGAGGAAA | 7088 |
rs551545201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614018 | GTTCACGCCATTCTC[C/T]TGCCTCTGCCTCCTG | 7088 |
rs551559103 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81658013 | CTCCCGGGTTCTAAG[A/G]AACTCTCCTGCCTCA | 7088 |
rs551599741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652159 | GCCATCAAATTAATA[A/G]GAAATGAAAGCTGGT | 7088 |
rs551612931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612398 | AAAATCCAATCCTGG[A/G]TTTACGTAAACCAAA | 7088 |
rs551620695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81670336 | AAAGTCCCTTCCCTT[C/T]TTTTTTTGAGACAGA | 7088 |
rs551681535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671085 | AGACAGGAGAATAGC[G/T]TGAACCTGGGAGGCA | 7088 |
rs551751828 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689100 | CTCGCCCTGCACGGC[C/T]GGACCGGCCGCTCCG | 7088 |
rs551753020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645802 | GGGATAGATACCCCA[C/T]TCTTTATGATGTGTT | 7088 |
rs551763982 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689593 | AGCGCCGGCCCCGCC[C/T]AGCCCCGTTCGGGCG | 7088 |
rs551815001 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81611000 | ACAAATGAATCTTAA[A/T]GTCACCGCAAACTAG | 7088 |
rs551840818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655235 | CGGGCGTGATGGTGG[A/G]CGCCTGTAATACCAG | 7088 |
rs551883062 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81592169 | CGAGACCATTCTGGC[C/T]AACATGGTGAAACCC | 7088 |
rs551895423 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81684888 | ATCGAGGGTCCTTTG[C/G]GCTGAGCAATCATTT | 7088 |
rs551905768 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81584647 | CATGCCCTAAGGACT[C/G]GTCCATGATATGAAC | 7088 |
rs551911490 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81611645 | GGCGTCTTTGTCTCC[A/G]AGGTGTGTGGGGCTG | 7088 |
rs551977841 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636928 | GAATCATTTGAACCC[A/G]AGTGGCAGAGGTTGC | 7088 |
rs551982443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619940 | AGACATTGAGCTCTG[C/T]CTTGAGAAGTACCAT | 7088 |
rs551982571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626405 | AATCAAGCCATCACC[A/C]TGCGCTGCACTTTTT | 7088 |
rs552012823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673130 | ATACAAAAATCAGCT[A/G]GGCATGGTGGTGCAC | 7088 |
rs552019213 | snp | C/T | 6.65956e-05 | 0.00577004 | intron-variant | TLE1 | GRCh38.p7 | 9:81620590 | TAATCAAAGATTTCT[C/T]CCCAAGCCTCTTTGT | 7088 |
rs552021948 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613618 | ACTGGGCACCTTCTA[A/G]CTACTCCCTCAGCCA | 7088 |
rs552038134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587415 | TTCAATGTACAAATC[A/C]CTTAAACAAACTCAT | 7088 |
rs552076205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673442 | CAAAAACAAAACGGA[A/C]GTATCAGTGAAGCAT | 7088 |
rs552111913 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81616240 | AGCTGAAAGTCCTTC[A/G]GGTTGGGGTTGTACA | 7088 |
rs552115944 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680078 | CTCCTCAATTTGCAC[A/G]CACGAGGTGCTGGGT | 7088 |
rs552128770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624457 | CACTGCAGACACCTC[C/T]TCCTAGAGTCTATAC | 7088 |
rs552139434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611237 | AGACAGCCTGCCCCC[A/G]TGGTTCAGTCTGTCC | 7088 |
rs552167581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618104 | CTGAAAAAGTCTACC[C/T]TCTTAGCCAAAACGT | 7088 |
rs552229263 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81660476 | TGGAGAGCAGTGGCG[C/T]GATCTCGGCTCACTG | 7088 |
rs552265397 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589501 | GCTACCCCATTCTAT[C/T]CAACAGGTATTTACT | 7088 |
rs552266297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81654995 | TAACAAACTCAAAGA[C/T]CTCACCGACAGGGCC | 7088 |
rs552273231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81606914 | ATATGGCTCAAACAT[C/G]AAAGAGAATCCTAAA | 7088 |
rs552292553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81623820 | TGAAAAATAAAAATC[A/C]AAAAAATAAAAATGG | 7088 |
rs552314081 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81618903 | ATGTCTGTCATCAGT[A/G]ATCTAAGGTCTGAGG | 7088 |
rs552342356 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683675 | CTGTCAGCATTTCCA[A/G]TATCAACTAAATTTC | 7088 |
rs552367279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81593900 | TACCTTGGTCAGGAA[C/T]GCCATTATATAAAAC | 7088 |
rs552371090 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611364 | CTCAGACATTTTTTC[C/G]TAAGGTTTAATGAGA | 7088 |
rs552376515 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81622460 | TTTTTTGTTGTTGTC[A/C/G]TTTAATGATGTCAAA | 7088 |
rs552376817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630115 | TAAATAATATGTTCA[A/G]TATAGAAAGACAAAC | 7088 |
rs552402108 | in-del | -/CTC | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81665461 | GATACTATCCTTTCA[-/CTC]CTCATCTTTCACACT | 7088 |
rs552408443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588511 | GCTGAGGCAGACCCA[C/T]GGGCACCTCAGCAAG | 7088 |
rs552418954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597966 | GGAAAACAGGTGTTT[A/G]CAGGGTTGTTGGTTT | 7088 |
rs552426074 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81622899 | GGCCCACGCAGCTGC[C/T]GGACGCCCGGCAGGC | 7088 |
rs552427892 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81592154 | ACAAGGTCAGGAGAT[C/T]GAGACCATTCTGGCT | 7088 |
rs552430923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631398 | CCTATTCACACCCCT[C/G]GCATTTCAGAGAGGC | 7088 |
rs552515416 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642485 | TCACCTGAGGTCAGG[A/T]GTTCGAGACCAGCCT | 7088 |
rs552664139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674685 | GAACAAAGAGAGGAG[C/G]ACTTTGTAAGGGGAG | 7088 |
rs552664565 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81667991 | CAACATGGTGAAACC[A/C]TGTCTCTATTAAAAT | 7088 |
rs552672091 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617754 | ATGTGGGCTGGGCGC[A/G]GTGGCTCAAGCCTAT | 7088 |
rs552687332 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663565 | GTGCCTCTCATCTGT[A/C]AATGACAGGGTCACC | 7088 |
rs552701872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81637219 | ACAAATTAGCCGGGC[A/G]TGGTGGTGCATGCCT | 7088 |
rs552727752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668649 | AGTGTCGTATGGGAC[A/G]GAATCTATTCAGAGT | 7088 |
rs552752197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639108 | GCTAATTTTTTTTTA[C/T]AGAGATGGGGTCTCA | 7088 |
rs552777935 | snp | A/C/G | 0.000345938 | 0.0131475 | missense, synonymous-codon | TLE1 | GRCh38.p7 | 9:81593205 | GGGGATTCCGGGTCC[A/C/G]ATGAGGGCGTCGGGG | 7088 |
rs552854290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674286 | CTATTGTGTCTGTGC[A/G]TGTCAATACACTGGC | 7088 |
rs552876119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81632112 | AAAAAGACTATCTAT[A/G]GGAACCCTGGAATGG | 7088 |
rs552897575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649106 | AATTTGCTGTCAAAG[C/G]TGTTTAAAAAAAGGT | 7088 |
rs552923280 | snp | G/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686872 | ACCATCACCAATGAT[G/T]GGCAATGTTATAAGC | 7088 |
rs552934280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643700 | CCACCACACTCAGCT[A/G]ATTTTTTTGATTTTC | 7088 |
rs552935284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672104 | AAGAGCCATGAACGC[A/G]GAGCTTCTCAGCACA | 7088 |
rs552946804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614197 | ACAGGCCTGAGCCAC[C/G]GCGCCAGGCCAGAAG | 7088 |
rs552973741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81658160 | CAAGTGATCCACCTG[C/T]CTCAGCCTCCCAAAG | 7088 |
rs552982440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638938 | CGATACATGCATTTT[C/T]TTTGAAGCAAAGTCT | 7088 |
rs552990096 | in-del | -/CA | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81640529 | ATAAAGAGATCAGTG[-/CA]CACTTGCTCTAACCA | 7088 |
rs553024995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671422 | GAGGCCAAGGTGGGC[A/G]GATCACAAGGTCAGG | 7088 |
rs553034672 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665583 | AATTGCTCCCATTCT[A/C]TAGCTCCTCGTGAGG | 7088 |
rs553083579 | snp | C/G | 1.65217e-05 | 0.00287412 | intron-variant | TLE1 | GRCh38.p7 | 9:81584352 | TGTGGAACAACGGTA[C/G]TCAGAGGCCCTGCTC | 7088 |
rs553119471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664906 | TCCCAGGTGACCCTG[A/C]GGCTCTTGGACTGGG | 7088 |
rs553158391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590644 | CTGTAAGCCCCCCAA[A/C]GGCAGCAACACAGTT | 7088 |
rs553162111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677030 | TCACTTGAGGCCAGG[A/G]GTTCAAGACCAGCCT | 7088 |
rs553162368 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605378 | ATGGACTTGGATTTG[C/G]TATCTTTTCCCTCCT | 7088 |
rs553180880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81633444 | ATAAAAAAAAGGGGG[A/G]AATAATTAGAACACA | 7088 |
rs553229474 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644129 | GAAATTGGAATTCTC[A/G]TACGCTATTGTGGGA | 7088 |
rs553229491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619798 | TGTGGTTTTAGCTGG[A/G]TCTGTGACAAGAGCC | 7088 |
rs553233069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81595688 | GCCGGGTATGGTGGC[A/G]GGCGCTTGTAGTCCC | 7088 |
rs553251182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81670515 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATATT | 7088 |
rs553275656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675825 | CCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGATGA | 7088 |
rs553289386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682498 | TGACAATTTATAGCA[C/T]GGCTTCATCAGCATG | 7088 |
rs553396657 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81596856 | TACACAGGTGGCTGC[C/G]TTTGGTGAAAAGTCA | 7088 |
rs553403703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628668 | TTGTCATAATTATCT[C/T]TAGGCAAGTTCTAAA | 7088 |
rs553423840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673828 | AACCCAAAAAGCCGA[A/C]TTCTGAAAGCCAAAG | 7088 |
rs553456295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587987 | AAGATCAAACTAACC[C/T]TCCCCTGAGGAGGAG | 7088 |
rs553457918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634307 | ACTGCTGCTGCTGTT[A/G]GTGGTGGTGGTGAGA | 7088 |
rs553502343 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586385 | GAGAGTGGAGCCTAT[C/T]GCTTGTAGGCTACAA | 7088 |
rs553530660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626876 | GAGCAGACAATAAAT[A/T]CAATTATTTAAAATT | 7088 |
rs553582290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643975 | TCCACTACAAAAACT[A/G]TACAGGTTTTGATTG | 7088 |
rs553593808 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81602218 | GGCTCATCCCATTGT[C/G]TTAGCACAGGATGTA | 7088 |
rs553598871 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81643054 | AGCAGAGAGTAGAAT[C/G]GCGGCTGCCTTGCGG | 7088 |
rs553630678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655057 | CTTAGTGTCTATAGC[A/C]CGGGCTGTTTTAAAG | 7088 |
rs553664178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81601517 | TTAGCCTGAGTTATT[A/G]CTGACCTCTAGGTGC | 7088 |
rs553718437 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632738 | CACACAGCCCTGTCC[A/G]CTGAATTTCCTTCTT | 7088 |
rs553756105 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606139 | GATGCTGGAGAGGAT[G/T]TGGAGAAATAAGAAC | 7088 |
rs553775653 | snp | C/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81600401 | GTCCTCCCAGCTACT[C/T]AGGAGGCTGAGGCAG | 7088 |
rs553776336 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81668183 | GAAAAAAAAAAAAAG[A/G]AGGATATGTAAAGGA | 7088 |
rs553798821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592929 | AAGGGGCTTCTATTT[A/C]CTCATAATGGGAATA | 7088 |
rs553836376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644929 | AACCCGGGAAGCGGA[A/G]GTTGCAGTGAGCCGA | 7088 |
rs553886484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643273 | CAGAGTTTCGCTCTC[A/G]TTGCCCAGGCTGGAG | 7088 |
rs553891164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681302 | TGCCTGTAATCCCAG[A/C]ACTTTGCGAAGCCGA | 7088 |
rs553894846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81636786 | AAGGCAAGTGGATCA[C/T]GAGGTCAGGAGTTCA | 7088 |
rs553922539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612040 | TGGCCTCATCATTTG[C/T]TAGTGTCACTCATGG | 7088 |
rs553932441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684979 | ACCATTATAGTAGCC[A/G]TAAGTGTGAATTTTA | 7088 |
rs553936059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81630610 | TCAAGGGTATCAAGA[C/T]CATGAGGCCATAAGG | 7088 |
rs553980644 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81655267 | TACTCGGGAGGCTGC[A/G]GCAGAGAACTGCTTG | 7088 |
rs553997683 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81604998 | CTTTTAATGACATCA[A/T]CAAGCCCCCAAGGGC | 7088 |
rs554051693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648567 | CTCGATTATCTGTGA[C/T]GTAAAGAGAACAATA | 7088 |
rs554058558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604552 | GATTCAGCTCAAGGG[C/T]TAGAAGAGTTTTCAC | 7088 |
rs554066210 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689186 | TCGTGTGCTTCTCCG[C/T]AAAGGGCGCTCCAGC | 7088 |
rs554128527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668977 | CTTCCATTAATTATG[C/T]GGGTTCCAGGACATG | 7088 |
rs554164132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81594551 | TACGTCTTAAAAAAA[A/C]AAAAAATTATGCACA | 7088 |
rs554169965 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684563 | AATGAAAGTCTTTGA[A/G]TATAAGGAAGATCTG | 7088 |
rs554198205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609637 | TTTCCTGCTTCCCCA[C/T]GAAGCCACTTTGCTT | 7088 |
rs554205588 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81680698 | GGCTCTAAATGCAGA[C/G]AGCTTTCTCTCTTTT | 7088 |
rs554233402 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653766 | TTCCACAGGAAAAAA[A/C]ATTAATTTGGGGGTT | 7088 |
rs554258194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81644620 | ACAGGGTGACAAAAA[C/T]GTTCTAGAAAAATTT | 7088 |
rs554276584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686484 | GATATTATCTACAAG[C/T]AGACAAAAGGTCAAT | 7088 |
rs554299980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596966 | TATTCAAGAGGAAGT[C/T]GAGGGGAAGGCTCGT | 7088 |
rs554324034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651074 | GATTAACTGGTTCCA[C/T]TGTCTGTGGCCGTCA | 7088 |
rs554359646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81615035 | TGTAATAAGCCAAGA[C/T]TGCACCACTGCACTC | 7088 |
rs554370667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676187 | CGTTCAGGGTCCAAA[A/G]TGGATACAACTACCA | 7088 |
rs554398406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688079 | CCCCAGGAAGAGAGG[A/G]CCCCAGACCTCCCCA | 7088 |
rs554411581 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81661515 | TCCACCAGCATTAAA[C/T]TGCAAATTGATGGAT | 7088 |
rs554421105 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TLE1 | GRCh38.p7 | 9:81585116 | AACTAAGTGTCTGCG[C/T]ATACCTAAATATCGA | 7088 |
rs554423239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81609656 | GCCACTTTGCTTTTT[A/G]TAATTCTAGATCTCT | 7088 |
rs554452354 | snp | A/C | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690150 | CCTCAGATCTAAGTG[A/C]AAGTAACTCAAAGAC | 7088 |
rs554455800 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680261 | TTCAATGAACTACAA[A/C]GGAACCAAGTCAGAG | 7088 |
rs554499299 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81617691 | TAGCCGACATAGCAA[A/G]ACTCTGTCACAAAAA | 7088 |
rs554509954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655663 | ATGCTTACTAAATGC[C/T]ACCTATATTACTGAA | 7088 |
rs554535299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664381 | GAAGAGTTCTTTGCC[A/G]AGAGGCCTCCTTCAG | 7088 |
rs554555027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624608 | TACTATCCTGACTGA[C/T]GTACTCTAATTCCAG | 7088 |
rs554584678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81654554 | CACCGTGTTAGCCAG[C/G]ATGGTCTCGATCTCC | 7088 |
rs554586831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81660573 | TGCCTGCTACCACAC[C/T]CGGCTAATTTTTTTT | 7088 |
rs554600000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683071 | TTTAAAACTTCCAGA[C/T]AGGAAAGTCAGCAGT | 7088 |
rs554607147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611427 | TTCTGTGAACCACTC[A/G]AATCATTTCATCGCC | 7088 |
rs554614763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81620838 | GTTTGAGAAATAGGA[A/G]CTTGCTGTGTTGTAT | 7088 |
rs554717738 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584081 | TAGTTTTCTGTCAAG[A/G]TTTGGAAACAGGTGT | 7088 |
rs554722435 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81630390 | CTCTTCCCACTATAA[-/T]TTTTTTTTGCTTTGG | 7088 |
rs554727056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653539 | TATCATCCACCCCTT[C/T]AAGGACAGCATTAAG | 7088 |
rs554734179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621453 | TACTGCCCTGAACAA[C/T]GTTGAATGAGCTGTG | 7088 |
rs554837860 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81613087 | AGGCAGAGGTTGCAG[A/T]GAGCTGAGATCACGC | 7088 |
rs554849655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659131 | CCAGGATGGTCTCGA[A/T]CTCCTGATCCTCGTG | 7088 |
rs554876039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622218 | CTAGTTTACTTCAGC[C/T]CCGAGGTCTCCTCCT | 7088 |
rs554893848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81627511 | CCTTTGAAGGGTTCA[C/T]CCTATTCACAGCAGT | 7088 |
rs554908205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81658341 | ACTGGATAAGCCTGA[A/G]ACAGGAGGAGAAAAG | 7088 |
rs554942161 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595540 | TTAAACAATTGAGGC[C/T]GGGCGCGGTGGCTCA | 7088 |
rs554955827 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659403 | TTTGGTACCCACTAA[-/G]TCATAATGCTTATAA | 7088 |
rs554957220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596699 | GGACATGGAAATGAC[C/T]GCATTTCTAGAATTT | 7088 |
rs554967919 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638087 | GCTCAGCTAACCAGA[C/T]GCTCTTGAGAACACC | 7088 |
rs554980280 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592813 | TATTTTTTAAAAAGA[A/T]ATCCATCAACTCTGG | 7088 |
rs555014952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81666595 | GCCTGACTAACATGA[C/T]GAAACGCAGTCTCTA | 7088 |
rs555018141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610851 | GGGTCTAATTTAATG[A/C]TTAAGGATTCATACA | 7088 |
rs555051210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662692 | AACAAAAGTGAAACT[C/T]CGTATCAAAAAAAAA | 7088 |
rs555060712 | snp | A/G | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589829 | GGCCCTGGCTCCATC[A/G]TTCCATTTTGCTCAC | 7088 |
rs555077479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587031 | CATTTAAAATGGCAA[A/G]CACTGTTTTTTCCAA | 7088 |
rs555093217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622624 | TTACTACTGTAATTT[A/C]CGCTTGAGCGGCTTA | 7088 |
rs555112722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638876 | GTGATCCTCCCACTC[C/T]GGCCTCCCAAAGTGC | 7088 |
rs555113554 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639807 | CAGGCTAGTCTCGAA[C/T]TCCTGGCTTCGAATG | 7088 |
rs555185634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678643 | AACATGGCAAAACTC[C/T]GTCTATACTAAAAAC | 7088 |
rs555217422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81625184 | GACTCTCTCTCTCAC[A/G]AAAATCTGGAATTCT | 7088 |
rs555323713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676959 | CTTACAAATTTGGCC[A/G]GGCATGGTGGCTCAC | 7088 |
rs555329324 | in-del | -/ACA | 0.00636936 | 0.0560724 | intron-variant | TLE1 | GRCh38.p7 | 9:81649328 | AAGCACAGAAAAAAT[-/ACA]ACCTCTCTCTGTCTC | 7088 |
rs555331404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599877 | CTCTTTGTTTCCTTA[C/T]TTAGAGGCATACACT | 7088 |
rs555377742 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81670906 | GGGTGCCGTGGCTCA[C/T]GCTGTTAATCCCAGC | 7088 |
rs555385869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619392 | CAGAGATACTACAGC[G/T]GGCTCCAGCAAATCA | 7088 |
rs555418800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613219 | AAACCCCAGGACAAA[C/T]ATCTGTTTCTTATCA | 7088 |
rs555441068 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81645319 | AGTGAGCGCCAAGAT[A/C]GCGCCATTGCACTCC | 7088 |
rs555442286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589908 | CCACACGCAGGGACC[A/G]GGCCCGGCTCAATGA | 7088 |
rs555448306 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671538 | TAATCCCAGCTACTC[A/C/G]AGAGGCCAAGGCAGG | 7088 |
rs555519571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675036 | AAAGTACATGGAAAT[C/T]CCTGCTTCATGTTAT | 7088 |
rs555549537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682057 | TCGAAACCAGCCTGC[A/G]AACATGGGTGAAACC | 7088 |
rs555561614 | snp | A/G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584390 | GGCACCTTCACTCCT[A/G/T]GCTTCAGAGGCGACA | 7088 |
rs555628493 | snp | C/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690593 | ACGTTTTGCCCGGGG[C/T]GCGAAATCCCAGGTC | 7088 |
rs555639648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645572 | ATGGAGAAACCTCGT[C/T]TCTACTAAAAATACA | 7088 |
rs555651546 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666198 | GGGCTTAAAGGAAAA[G/T]GCACTCTGTGGTGGA | 7088 |
rs555712779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81601416 | CACTAAACAAGTGGG[C/T]AGAAGATTTCTAAAT | 7088 |
rs555734144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81598032 | AACAATAATGAAGAA[A/C]CACAGACCCCAGAGA | 7088 |
rs555773054 | snp | A/G | 4.94768e-05 | 0.00497352 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81633355 | GTACTTACTGTGCCC[A/G]GCTCTCTGTCTGCTC | 7088 |
rs555776723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592712 | TCAGAGTCCAGGCCC[A/G]GTTGTGCTTTTGTCC | 7088 |
rs555807341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684939 | GTCCTTAGTGCCTTG[C/T]TCCAGCTCAATACTC | 7088 |
rs555824806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646089 | CCTATGAAACAAACC[A/T]GCACATCCTATACAT | 7088 |
rs555833764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596289 | TGTGAACACTCATCC[A/G]TCCCACGGGAAGCCC | 7088 |
rs555930019 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688876 | CGCAGCGGAGGCTCC[C/T]GGCCGGGGAGCGACG | 7088 |
rs555934619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81640133 | GGACAGCCCTCACCA[A/C]AGAGAATTATCCTGC | 7088 |
rs555935904 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687682 | CGCTAAGTGCGCCCG[A/G]GTCACCAGGCCAAAG | 7088 |
rs555944525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684538 | ATTCAACTCTGAAAC[A/C]CACTTGCTTAATGAA | 7088 |
rs555945432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604924 | TTACATGTCTCCCTA[A/T]CACCCACTGCTCTGC | 7088 |
rs555951759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678773 | CTACTCAGGGAGGTA[A/G]AGGTTGCAGTGAGCC | 7088 |
rs556009483 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81651165 | GAGGGAACTATAAAG[A/T]CCAGCAGGGCATCAT | 7088 |
rs556043597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630285 | ATACCACAAAAGAGC[A/G]AATGCAGAGGATGAG | 7088 |
rs556051312 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81613648 | AATTTTCATAAATCC[A/G]CACAATGTTGACAGC | 7088 |
rs556130508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81630528 | AAAATCAAAATATTA[A/G]CCTAGTAAATATCAA | 7088 |
rs556131965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612493 | CTTTCCCACTGGGGA[A/G]TATCAGGTTGCAAAT | 7088 |
rs556195256 | snp | C/T | 0.000101605 | 0.00712688 | missense | TLE1 | GRCh38.p7 | 9:81611858 | AACTGGCGTAGGCAG[C/T]GCCTGGGCTGGTCAG | 7088 |
rs556229473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610377 | CTGTTCATTAGAAAC[C/T]CACAGATCCCCAAAG | 7088 |
rs556245920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649948 | TCACCACAAACTTGA[A/G]AAGAGCCTTCGGACA | 7088 |
rs556274423 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690189 | GAGTTTCTTATTGGA[C/G]GCGGAGGGGGGCTTT | 7088 |
rs556303240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81606476 | GTCCTTTGCAGGGAC[A/G]TGGATGAAGCTGGAA | 7088 |
rs556304763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610767 | CCACCCCCAGTTATG[A/T]TAATCAAAAGTGTCT | 7088 |
rs556318219 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81617250 | AATAAACCTTTTTAG[C/T]AATCAGCTTGAAGTA | 7088 |
rs556326462 | snp | A/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586560 | GGTCTGTCCTTGGCT[A/T]AAAGGTTATATGGTG | 7088 |
rs556330586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643242 | TTGTTTTTTGTTTTT[G/T]GGTTTTTTTTTTTGA | 7088 |
rs556345399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604454 | TGAAGAGCTGCCATG[A/G]GGATGATAGATTAGC | 7088 |
rs556350272 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81680513 | AACTATGTTTTGTGA[-/T]TTTTCTTAAAATCCA | 7088 |
rs556406803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649759 | TCCCGGTACCTCCTC[C/T]CCTCTGGGGAGACAG | 7088 |
rs556407379 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81682527 | TGCTGAAAAGATAAC[-/AT]GAGTGGGCTAAAATA | 7088 |
rs556445740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81654365 | TGTATTTTTGAGACA[C/G]AGTCTTGCTCTGTCG | 7088 |
rs556463560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81623908 | ACCACTGAGACATTT[C/T]GTTCCTCTTCCTCCT | 7088 |
rs556499398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646154 | AAGGAAAGAAATATG[G/T]GGGGAAATTAAAAAG | 7088 |
rs556522071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614949 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG | 7088 |
rs556540001 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614009 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 7088 |
rs556593998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686035 | AAACACCCAAAAGCT[C/T]TGTCCTTGCATTTAA | 7088 |
rs556601365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686393 | AAAATATGTCAAGTA[A/G]CTACTGCAATAAAGT | 7088 |
rs556633123 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684678 | ATAGCACATATACAT[C/T]AAGTAAGAATTGTAT | 7088 |
rs556637963 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81649577 | ATAGATGTCTAAACC[A/G]TTAAATTACTATTTC | 7088 |
rs556643684 | snp | A/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686782 | GACTCCACTCTCTCA[A/T]CCTACCCAAACCAAT | 7088 |
rs556667534 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81609079 | CCCCTTTCCTCTCCT[C/T]TCCTTTCCTTTCCTT | 7088 |
rs556677325 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656651 | ATACCAAGGGGTTTC[C/T]GTTACATACCCTGCC | 7088 |
rs556684240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614337 | TGCCTAAAAAGAACA[A/C]CACTTTGGAGTTAAG | 7088 |
rs556715833 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81655979 | AAGTCTTTGGTTTTA[C/T]AAGATTGGATTTAGT | 7088 |
rs556767714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81658305 | TACAAAGGGCCGACT[A/G]TACTATGTAAGTTGG | 7088 |
rs556824216 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629094 | TAAAATGGATCACTG[C/T]AAAATGATAGCAAGT | 7088 |
rs556842746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661357 | CCTCAGCGCCCGCAC[A/T]CTTCCCCACTACACA | 7088 |
rs556875233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652928 | ATTCTTTTATAGCCT[G/T]TTGATTCTTTACCCT | 7088 |
rs556938290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609377 | GGCGTGAGCCACTGC[A/G]CCTGGCCTCTGCTAT | 7088 |
rs556967868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632659 | ACTGGCAGATGCATG[C/T]ACAGATCAAATGTAC | 7088 |
rs556983003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81659753 | CTAGGGGTTCTATGT[C/T]AAATCACTTAAACCA | 7088 |
rs556987617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687814 | AAAACAACTCCTTTA[C/T]GCTCCCCATTCCCAG | 7088 |
rs557073918 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645022 | AAAAAAAAAAAAAAA[-/AA]GGTGAATTTCATGGT | 7088 |
rs557086770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626742 | GCTGTGCAGGTGACA[C/G]ACAGGGCCGGTTAAT | 7088 |
rs557105315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81641779 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGTG | 7088 |
rs557149406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585821 | CGCAGATGAACCAAG[C/T]GTCAAAACCTTTAGG | 7088 |
rs557150259 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584083 | GTTTTCTGTCAAGGT[G/T]TGGAAACAGGTGTTT | 7088 |
rs557174228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676866 | GAATGTGTGCTGACA[G/T]TTCATTTTACCACTG | 7088 |
rs557186177 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669550 | TCATCTGCAGTGTAG[A/G]GGCATGTGCCAAAAT | 7088 |
rs557189481 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81590082 | TTCCCAGCAAAGATG[A/T]AACAAGAGTAAAACA | 7088 |
rs557230150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81646571 | CTCATAAGAATAAGA[A/G]GCCAACCTCATCCTC | 7088 |
rs557244095 | in-del | -/C | 0.0227684 | 0.104239 | intron-variant | TLE1 | GRCh38.p7 | 9:81667719 | CTGTATTCCTGCTCC[-/C]CCCCCAAGCTGAGTG | 7088 |
rs557251940 | snp | A/C/G | 0.00058434 | 0.017083 | intron-variant | TLE1 | GRCh38.p7 | 9:81633299 | GGACCGTGTGTGTGT[A/C/G]TGTGTGTGTGTGTGT | 7088 |
rs557257733 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81637637 | TGCTTGGCTACAATG[A/G]AAGTTTCTTTTTTTT | 7088 |
rs557280092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628042 | TAGGCAACATACTGA[C/G]ACTCTGACTGTACAA | 7088 |
rs557303989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81663581 | AATGACAGGGTCACC[A/G]TGCCCTTGCTACCCT | 7088 |
rs557308069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671289 | AAGGCTGAAGCGGGC[A/G]GATTGCTTGAGCCCT | 7088 |
rs557313229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672163 | GCTTGTTTGAGAGCA[A/G]GTACTGGCACAACTT | 7088 |
rs557356819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669573 | GCCAAAATCTCCTCA[C/T]TTGTACATGCAAATA | 7088 |
rs557380227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672833 | TGATAGAATGAACCA[A/C]ATCCTTTGTTGTTCT | 7088 |
rs557390995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81673142 | GCTGGGCATGGTGGT[A/G]CACGCCTGTAATCCC | 7088 |
rs557397894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615738 | AAAAAAAGAAGAAGA[A/G]GAAGAAGAAGGCAAT | 7088 |
rs557445092 | snp | A/T | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81669076 | TTGTGTGGTTCCCAC[A/T]GGGCTGGGTTGGCTC | 7088 |
rs557458520 | snp | C/T | 0.00079936 | 0.019976 | intron-variant | TLE1 | GRCh38.p7 | 9:81628776 | AACTAAGTATGTGAC[C/T]GGATGCACCCAGCCT | 7088 |
rs557465297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591986 | CAGACACCACACCAG[A/G]GCAGGGCAGGGCAGG | 7088 |
rs557481909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644412 | AAATACTGGTGATAC[A/G]ACAACATGGATAAAC | 7088 |
rs557519223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674970 | GACCATCCTGGACAA[C/G]ATAGTGAGACCTCAT | 7088 |
rs557540172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634928 | ACCCAGTAATCTGGG[G/T]GGGTGTCTCATGCAC | 7088 |
rs557541253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81594458 | AACCCTGCATGTTCT[C/T]ACTCATAAATGGGAG | 7088 |
rs557559895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638037 | AAGGAAAAGGGCAAA[G/T]CCATTCTCTACTGAG | 7088 |
rs557569094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81683595 | TTCAGAAGGATGTTT[C/T]TCAAATGTAAGTCCA | 7088 |
rs557574494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677970 | GGATAGAATTTTCAG[A/C]ATTTGTTTTTTCCTC | 7088 |
rs557580836 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614926 | GAGGCCAGGTGCGGT[A/G]GCTCACACCTGTAAT | 7088 |
rs557583149 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81596924 | TGTGTATGGTATTCC[A/T]ATATTTAAAGTTTAG | 7088 |
rs557598574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631681 | AAATTGAAGTCCCAA[A/C]GCTAGAATAAGTTCA | 7088 |
rs557644913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81643988 | CTATACAGGTTTTGA[C/T]TGAAAAGATGTTCAA | 7088 |
rs557752751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624660 | TTCACCTTGCAGCTG[C/G]TAAAATGTAAATATC | 7088 |
rs557767569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81595713 | AGTCCCAGCTACTCG[G/T]GAGGCTGAGGCAGGA | 7088 |
rs557791526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81625129 | ATGATTAGATGAGGT[A/G]CAAGAACACAGAAAC | 7088 |
rs557791542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618324 | GCAAATATTATCCAC[A/G]TTGGCCTTCTGAAGT | 7088 |
rs557792779 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675294 | TTTTTCATAATAAAA[C/T]GTTTGGGAGAATGGA | 7088 |
rs557827647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81631228 | GGACAACCAATAACC[C/T]TCCCTCCACCCACTC | 7088 |
rs557873587 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647218 | CACTGGTCATCTGAC[A/G]ATGTCTTCTAACTCT | 7088 |
rs557882448 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625213 | CTGTGAGAACACCAG[A/T]TCTCAAGAGGGCATC | 7088 |
rs557888746 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81637416 | ACTGTGAAGAGGTGA[C/T]GGCTTACATAATGGG | 7088 |
rs557909758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680098 | AGGTGCTGGGTTCTG[C/T]GGGTGTATGCTGGGA | 7088 |
rs557919027 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690921 | ATAATCAAGACATGC[C/T]GTATAATTAATGCTG | 7088 |
rs557957493 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670664 | ATTGTTACTTATTCC[G/T]TATTAACTTTGAGCA | 7088 |
rs557961225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686346 | TACAATTGCTGGTCC[C/T]TTTCAAAACCTTTGG | 7088 |
rs557965027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81593485 | CGTGTACCAAATGAC[A/G]TATATATTGAACTGT | 7088 |
rs557980039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675873 | GCCCAGCTAATTTTC[A/G]TATTTTCAGCAGAGA | 7088 |
rs557995627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685985 | CTTCAAGTAAAAACA[C/G]AGACCAATTTGGAAA | 7088 |
rs558015732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662624 | AATAGCTTGAACCCA[C/T]GAGGCAGAGGTTGCA | 7088 |
rs558045899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605624 | AAAATTAATTCAAGA[G/T]GGATTAAAGATTTAA | 7088 |
rs558058275 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81584794 | TAACCCTCAAATATA[A/G]AAATCAATGAAGAAT | 7088 |
rs558089446 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81607305 | CTTTAATAAGCATGA[C/T]ATTACTTCTGTCTTA | 7088 |
rs558094717 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668288 | GTTAACAGTCAAGAA[A/G]TTTTATTTTCTCAAA | 7088 |
rs558124984 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81599361 | TGACGTTATCCCCTC[A/G]AGAGGGATAACGTGG | 7088 |
rs558128022 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81604391 | GAAGCGACAGACAAA[A/T]TCTAGCCAGAAGAGA | 7088 |
rs558128037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597304 | GCCAAGTGAAGATAC[A/G]TTGAATTGAGGGCTT | 7088 |
rs558192293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81607860 | TGACTCCCTTCATTG[A/G]GCACAGAGGTCATCA | 7088 |
rs558196229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81681346 | ACTTGAGGTCAGGAG[C/T]TCGAGACCAGCCTAG | 7088 |
rs558197198 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688780 | ACCCGACGCTTTCGG[A/G]GCGACTCCCGCAAGA | 7088 |
rs558222355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81635155 | CAGGGGAGAGGATCT[C/T]AGGGAGCCAGGCTTG | 7088 |
rs558243086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678152 | GGAGGGGATAAACAA[C/T]TGTGCCCACCATTAT | 7088 |
rs558309815 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81616578 | ACTTCCTTCATTCAC[-/TG]TTAGTTTTTTTTCAT | 7088 |
rs558332474 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688329 | GAGGAAAATTAAGCC[A/G]GAAAGCCAAGCAGAA | 7088 |
rs558334890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683797 | TAATGCATACAGGCT[A/C]ACGGACAGACAGTAT | 7088 |
rs558371527 | in-del | -/AAAT | 0.492435 | 0.0610346 | intron-variant | TLE1 | GRCh38.p7 | 9:81666776 | AAGACTCGTCTCACA[-/AAAT]AAATAAATAAATAAA | 7088 |
rs558387344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81641949 | ATTGCTTGAACCTGG[A/G]AGGCAGAGGTTGCAG | 7088 |
rs558397804 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588763 | CAGAAAAGGCGAGCA[-/C]AAGTCTAGACCCACC | 7088 |
rs558410735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586286 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 7088 |
rs558412983 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583714 | CTTTACTGTAATAAA[C/T]CAAATATATTTACAA | 7088 |
rs558415586 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81655148 | AGGCATGTGGATTAT[C/G]AGGTCAGGAGTTCAA | 7088 |
rs558470740 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632364 | TGTCTCAAAGACAAT[C/T]TTAAAAGTAGCTACT | 7088 |
rs558474624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612614 | AAAACCAGCAAACTA[C/T]AGTCTGCAAGGAGCA | 7088 |
rs558484607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81642530 | AACCCCGTCTCTACT[C/T]AAAAAAAAAAAAAAT | 7088 |
rs558495057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588489 | TTGGGCAGAGACACA[A/G]GTAATTGCTGAGGCA | 7088 |
rs558503120 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81684506 | AAAATCAAAGAGTGC[A/G]GAGTTACAAAAGCAG | 7088 |
rs558535292 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81659178 | CTCCCAAAGTGGTGG[A/G]ATTACAGGCGTGAGC | 7088 |
rs558627616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615154 | CAATGAACATGGATG[C/T]GTGTACACCCTCTCT | 7088 |
rs558653931 | snp | C/G | | | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590565 | TGGAGTCTGTATGTG[C/G]GCTGAAGAATTGGCA | 7088 |
rs558656467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617563 | AAAAATTAGCCGGGC[G/T]TGGTGGCGCATGCCT | 7088 |
rs558661156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81654292 | TTGGAAAATCTAGGC[A/G]GTTTAAGGCTATATG | 7088 |
rs558691195 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81630387 | GCCACTCTTCCCACT[A/G]TAATTTTTTTTGCTT | 7088 |
rs558693158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622720 | GGCTAGTAATTAGCA[A/C]CCCTGCTTATCTGAA | 7088 |
rs558704626 | snp | C/T | 7.74848e-05 | 0.00622386 | missense | TLE1 | GRCh38.p7 | 9:81611807 | CCACGGCGGCCGCGG[C/T]GGCTGCGGCGCTCAT | 7088 |
rs558719228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655441 | TCTGCTACAAGGGAC[A/G]AAAACTGGCAAGAGA | 7088 |
rs558729768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81623230 | GTTGTGATTTCTCCT[C/T]GTGCACTCCCTACTG | 7088 |
rs558784445 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661200 | TTTTTATATATATAT[A/G/T]TATTTTTATATATAT | 7088 |
rs558800093 | in-del | -/TACT | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81630851 | CAAAGTTTGAAGAGC[-/TACT]TAATTTTATGTAACT | 7088 |
rs558823310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614159 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 7088 |
rs558873834 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616636 | AAACTTTGATGAAAA[A/G]AATGGTTACCTCATT | 7088 |
rs558896711 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81611546 | ACAAAAACACTAAAA[A/C]AAAAAACGTTTGGCC | 7088 |
rs558911386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81660333 | CAGTGCTAGACAAAG[A/G]CTGTTCACAAAAAAA | 7088 |
rs558927228 | snp | A/G | 3.364e-05 | 0.00410108 | synonymous-codon, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587707 | AGTCGTGCTGCTGCA[A/G]CTGCCGCCCCTCGCG | 7088 |
rs558946556 | in-del | -/A | 0.0019495 | 0.03116 | intron-variant | TLE1 | GRCh38.p7 | 9:81593315 | ACAGAAAACACATTT[-/A]ACAGAGGAAGCAATC | 7088 |
rs558977978 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81682122 | AGCCGGGCATGGTGG[C/T]GGACACCTGTAATCC | 7088 |
rs558984633 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689284 | GCGCTCCGCCAATCG[G/T]CCACCCTCCCCGGCG | 7088 |
rs558987776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81650341 | AACGTCAGAGTTTTG[C/T]CATCATGAAATTATA | 7088 |
rs558989748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592584 | TCTCTCAGGTCTCCC[A/T]TAAAAACACAGACCC | 7088 |
rs558996705 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689734 | CGCTGACGCGCTCCT[C/G]CCCGGAGCGTATGGC | 7088 |
rs559009643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655078 | TGTTTTAAAGAAGGC[A/G]GGAAAGGCCGGGTGC | 7088 |
rs559012574 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638482 | CCATTTTTTCTCAAC[A/G]AGGCTTACCTGAGAC | 7088 |
rs559050968 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593975 | AGCCCAGCCTGCCTA[C/T]GTTCTGACCAATGAG | 7088 |
rs559071268 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637654 | GTTTCTTTTTTTTTT[-/C]TTTTTTTTAAGCAAA | 7088 |
rs559076740 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687128 | CAAACCGGCAAAAGG[G/T]AAACAATGGGAGGAG | 7088 |
rs559149912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656325 | GTAAAGGAGTAGAGA[C/T]GCCTTTGGTAGGTAT | 7088 |
rs559176352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592234 | GTGGTGGTGGGCGCC[C/T]GTAGTCCCAGCTACT | 7088 |
rs559182106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673678 | TAATTAGTATCCACA[C/G]AAAGGGAGGCTGGGA | 7088 |
rs559196814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81635951 | ATCACTGCAGCCCAA[A/G]AGTTTGAGACCAGCC | 7088 |
rs559206991 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684545 | TCTGAAACACACTTG[A/C]TTAATGAAAGTCTTT | 7088 |
rs559212013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624407 | CTTCATGGCATGCCA[A/G]TCACCAGAGGTAATC | 7088 |
rs559240849 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658010 | CACCTCCCGGGTTCT[A/G]AGGAACTCTCCTGCC | 7088 |
rs559243664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81667250 | AGAAATACAAAAATT[A/T]GCTGGGTGTAGTGGT | 7088 |
rs559246661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618835 | TTACCGTAATTTAAA[C/T]CTTAGCTTTGTACCG | 7088 |
rs559343567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592226 | AGCCGGGCGTGGTGG[C/T]GGGCGCCCGTAGTCC | 7088 |
rs559360356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669287 | CTTGACCTCAGACCA[A/G]TTTTCATCTCCATCT | 7088 |
rs559388557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81584617 | AACTAAGAACATTTT[C/T]AATATATGAACTATC | 7088 |
rs559413814 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81600926 | GATTATCAGTGCTAC[A/T]GGTTCTCAGGCCTCA | 7088 |
rs559426343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686752 | AGAAACTAAGGCTGA[A/G]ATGGATATAAATGTG | 7088 |
rs559447045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613267 | GGAAGGAGGGTGGCC[C/T]TACGTACATTTCATA | 7088 |
rs559518106 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691102 | GCACATCTTGGACAA[A/G]TATTTATCTTATGTT | 7088 |
rs559519095 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676720 | TGGATGTAATCCCAA[G/T]ACCCTGAAGACAATT | 7088 |
rs559524622 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81659891 | AAAGTGCTGTACAAA[C/T]ATGAGAGATCTTCCC | 7088 |
rs559551058 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | TLE1 | GRCh38.p7 | 9:81661766 | TTAAATCCCCCCCCC[A/C]AAAAAAATGTACACA | 7088 |
rs559580550 | in-del | -/AGGTGGATCACTTT | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81667184 | TCGGGAGGCCGAGGC[-/AGGTGGATCACTTT]AGGTCAGGAGTTTGA | 7088 |
rs559604411 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690726 | CTGGGAACAAAGAGA[C/G]ACAATGTAATAAACC | 7088 |
rs559618335 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684810 | AAAAAGTGAATGTCA[C/G]CGTATCTCCAGAATA | 7088 |
rs559626687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618060 | AAAATTCAATGATGC[C/G]ATCATCCCTACATCA | 7088 |
rs559652415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588856 | ACCATGCTGCTTCTT[C/T]CTCCAGGATCCCCAC | 7088 |
rs559692528 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583344 | TATTTTGCCTTCCAA[C/T]GAATCACCAGAAAAA | 7088 |
rs559706655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614638 | AATGGGATAATGCCT[A/C]CCGGGACCAGGTAAG | 7088 |
rs559728000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611174 | GTTTCTTCTTGTTCA[A/G]AAATTAGATCATTTG | 7088 |
rs559735263 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687795 | CCCCGGGGACCAGAG[A/G]AGAAAAACAACTCCT | 7088 |
rs559755674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81595600 | AAGGCGGGCGGATCA[C/T]GAGATCAGGAGATCA | 7088 |
rs559776182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81639300 | AGAACTCCTGGCTTC[A/G]AGCAATCCTCCTGCC | 7088 |
rs559784692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587342 | TCTCCTACTCCTGCA[G/T]TAGATGGTGAGAATA | 7088 |
rs559811879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652095 | CCTTATCAAATAGGT[C/T]AACGTTAAGATACAC | 7088 |
rs559905276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617449 | ACGCCTGTAATCCCA[C/G]CACTTTGGGAGGCCG | 7088 |
rs559908679 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81592134 | AAGGCCAAGGCGGGC[A/G]GATCACAAGGTCAGG | 7088 |
rs559915025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678816 | CTGCACTCCAGCCTG[C/G]ATGACAGAGCAAGAC | 7088 |
rs559919747 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81660779 | CAGCAATCAATCAAA[C/T]TCTAGTGTATTCTGC | 7088 |
rs559925163 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81673437 | GTTTGCAAAAACAAA[A/G]CGGAAGTATCAGTGA | 7088 |
rs559938304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632932 | CCAACTTCACAAAGG[G/T]ATTGTGATCTCTTGC | 7088 |
rs559945797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586643 | AATCCAGTGTCTGGG[G/T]GTGGGAACGAGAGTT | 7088 |
rs559953876 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627317 | AAAATTGTTCTCTCA[-/T]CTTTTTTTTTTTTAA | 7088 |
rs559957741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677992 | TTTTTCCTCCCAGCT[G/T]TTTCCTTCTACCCAA | 7088 |
rs559970440 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601825 | ACAAGGGATCTCCTT[C/T]AGAAAAGAATGAATC | 7088 |
rs559973577 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595712 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7088 |
rs559986303 | in-del | -/AAAA | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81655587 | GCTTTTTTAAAAAAG[-/AAAA]AAAAAGTCATCTGTA | 7088 |
rs560013549 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81639593 | TTTTTTTTTTGTTTT[G/T]TTTTTTTTTGAGACA | 7088 |
rs560066628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631349 | CACAGAGGTATAAAA[C/T]ACATCTCTACTAGCT | 7088 |
rs560084239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81660421 | TTTTTATTTTATTAT[C/T]ATTATTTTTTGAGAC | 7088 |
rs560107474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632317 | TCCTCACTCCTCCAC[A/G]CACATCCAGATACAT | 7088 |
rs560122434 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81610748 | TCCATACCTGCCCCC[C/G]CTCCCACCCCCAGTT | 7088 |
rs560165774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81666849 | AAGACAAAGGCCTGA[A/G]GCACTGGCTCACATC | 7088 |
rs560218411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622842 | CAGCAGAGTGTGGGC[G/T]GGAAAGGCCCAGAAA | 7088 |
rs560218971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81631309 | CAACAGGAGGTTATC[C/T]GACACATTCGGAAAT | 7088 |
rs560289694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81605275 | CAGCAAACACTGGCT[A/G]CTGTTTGCAGTGAGA | 7088 |
rs560341817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81636200 | TTCTTTATGCATAAA[A/G]TCACCTTCCTGTCAT | 7088 |
rs560346600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597375 | GAAAGGGAGGAAGAC[A/G]CAGGGTGGGGATCAG | 7088 |
rs560346816 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654543 | AGGTGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 7088 |
rs560364501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644058 | GATGCGGCCTCACAC[A/C]CATTAGGATGCGGAG | 7088 |
rs560469368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81635349 | AGCGAGCCAAGCCCC[C/T]GTTCCCAAATGCCTT | 7088 |
rs560500868 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81633970 | AGTGGAAAGCTTTGC[A/G]ACAGTTCCTCTTATC | 7088 |
rs560542040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686070 | GAAAAGGAATAATGT[A/G]AACAATACAAGGTGT | 7088 |
rs560610418 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81637203 | TCTCTACTAAAAATA[C/T]ACAAATTAGCCGGGC | 7088 |
rs560628111 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81639786 | ATGGGGTTTTGCCAT[C/G]TTGGCCAGGCTAGTC | 7088 |
rs560690659 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81679868 | TGGAGACCACAAAAG[G/T]TTTAATAATAAAACA | 7088 |
rs560709218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649659 | TTCTTTACCCTAAGT[A/C]GGCCCCTGAACAATA | 7088 |
rs560731574 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655221 | ATACAAAAATTAGCC[A/G/T]GGCGTGATGGTGGGC | 7088 |
rs560762681 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81609187 | CCACCCAGGTTCAAG[C/G]GATTCTCTGGTCTCA | 7088 |
rs560772054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596026 | GAGGCACCCTTTCAT[A/C]AATCTCAGATTTTTC | 7088 |
rs560772539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648997 | AAATTATCCTTTTCA[C/T]TGTGACAAGACTACA | 7088 |
rs560829373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655785 | TCCCAGGAACAAAGT[C/T]GAGCCTGCGGTGAGC | 7088 |
rs560857189 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649141 | AAAAATATTTCAATA[A/G]TCTCTCCAGTATCAA | 7088 |
rs560875205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677628 | CTTTTCACCAAGAGG[C/T]TGTACGTATACCTAG | 7088 |
rs560887856 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689529 | CGCCGCCGCCCGCGC[C/T]TCTCGCGCCGCTTAC | 7088 |
rs560888261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613877 | CACATGTCCTGGCCG[C/T]CAAGTCCAAGGAAGA | 7088 |
rs560926784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81596521 | CACTGAGGGCTCATC[A/G]TGACCATGGTGAAGG | 7088 |
rs560989961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602354 | GCTTCAGGACCAGAA[C/G]TGTTTCTGATGTCGG | 7088 |
rs560998726 | in-del | -/T/TT | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586019 | GTCGTTAGGTGACTT[-/T/TT]TTTTTTTTTTTTTTT | 7088 |
rs561001916 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81682610 | GGTAATATCAAACCA[C/T]ATGACAGACAAAAAC | 7088 |
rs561013501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81659788 | GTCCCAACCAGGTCT[C/T]GTACTTAACAGGATT | 7088 |
rs561016819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81646234 | CCGGACACTGAGGAA[A/G]AGTTCTGCATTTGTC | 7088 |
rs561022829 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81673792 | CTAATGTTGTCATTG[A/G]AAAAGCTTACTGTAA | 7088 |
rs561030298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651942 | ATACCAAGACCCCGG[A/T]CTGTTTAAAAAGAAT | 7088 |
rs561052623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653760 | GCAGTTTTCCACAGG[A/G]AAAAAAATTAATTTG | 7088 |
rs561098966 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585716 | TTAGGAAGGGAAGAC[A/G]CAATGTGAAAAGTGG | 7088 |
rs561135982 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81657743 | TCCTTTATATAAAAT[A/G]GTGTATTTGCATATA | 7088 |
rs561154863 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81624777 | TTTTCATTTAAAATT[-/A]AAAAAAATAAACAAA | 7088 |
rs561162065 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687931 | CCTGCCCCCACTCGG[A/G]GAAGGTAGAGGGGAT | 7088 |
rs561175964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81659371 | AAATAATTTTCCTAC[C/G]CAATGATGAATACCT | 7088 |
rs561226151 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679216 | GGTTATTTGATAAAA[C/T]CATATATCAACACTT | 7088 |
rs561230703 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81647085 | AAACTCAAATTTCTT[G/T]ATCTCCTGAAGTTCA | 7088 |
rs561242428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610465 | GAGGTAATATAAGCA[C/T]CCCTGAACGCCACAA | 7088 |
rs561244205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634467 | AGCCAAGAAAGAGAG[A/G]GAGGAAAGGGGAAAA | 7088 |
rs561282828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628157 | TTCACTGCCGTCTTG[C/T]TACTCTGCAAATGGC | 7088 |
rs561283159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604086 | CATTTCCTTGTGAAG[A/T]CTCCCATGTACACCT | 7088 |
rs561294445 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688373 | TGGCCACGCACGCGC[C/G]CTCCGCCGGGCGCAC | 7088 |
rs561356946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683953 | TACAGGAACCCAGAA[A/G]AATTACACACCTCTT | 7088 |
rs561365667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686704 | ATTTTACAAAAATTT[A/G]TAAGTCCTTTGAAGG | 7088 |
rs561372131 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653207 | GATGGTGACCATCCG[G/T]CATGGAGCAACAGGT | 7088 |
rs561414861 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81662198 | CATTTGCCCTCCTAA[C/T]AAATCAGTTGTCTAA | 7088 |
rs561414930 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591305 | GAAACTATCTAGGTA[C/T]GAGGTACAGGTGTAC | 7088 |
rs561467259 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81615277 | GAGGTTGCAGTGTGC[C/T]GAGATCACGCCACTG | 7088 |
rs561490944 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81685113 | GCCATAAAAAGATGC[-/T]TTTTTCACATCCACA | 7088 |
rs561492164 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81595751 | GTGAACCTGGGAGGC[A/G]GAGCTTGTGGTGAGC | 7088 |
rs561529963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81585415 | CTCGGAGAACATTTT[C/T]TCCAGATTATGATCT | 7088 |
rs561573025 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612927 | GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAATCCC | 7088 |
rs561574032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81650108 | GCATCCAGAGCTAAC[C/T]TGCCTTTATAATAAC | 7088 |
rs561576904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661619 | AGATAAAAACACAGT[A/G]GAGTGTTGGTAAGAA | 7088 |
rs561589799 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682226 | CCACTGCACTCCAGC[C/T]TGGGGAACAAAGCGA | 7088 |
rs561598621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672227 | TACAAAGACACACAA[C/G]AAGTTTCTACTGCAT | 7088 |
rs561648214 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81637591 | ACAGCTCACTGTCTG[A/C/T]TATTAGAGGTAACTG | 7088 |
rs561701793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81606118 | TTAAAAAGTCAGGAG[A/C]CAACAGATGCTGGAG | 7088 |
rs561713835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668410 | AGAGAGTAAGCAAAA[A/G]GATCCTAGATGACAG | 7088 |
rs561727355 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622263 | GCATCCACGGCAGGG[A/C]TGTATCTTATTCAAC | 7088 |
rs561749349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613298 | TTTGTAGGGCAATTG[C/T]GTCACAACATTAACA | 7088 |
rs561764598 | in-del | -/GAAAG/GAAAGGAAAG/GAAAGGAAT | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81642722 | AAGAAAGAAAGGAAA[-/GAAAG/GAAAGGAAAG/GAAAGGAAT]GAAAGAAAGAAAGAG | 7088 |
rs561781988 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81657013 | TCAATATTGAGTTTT[A/G]TTGACCTTCCTTTAA | 7088 |
rs561788773 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TLE1 | GRCh38.p7 | 9:81597266 | GACAGTATTGTTATC[A/G]CACCACCACGACTTA | 7088 |
rs561803739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81674558 | AAAATCAGAGTCCTT[C/T]TGCAAAATTATTTCT | 7088 |
rs561809430 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589533 | CCCAGGAGCCGGCAC[A/G]GAGCAAGGGTTCAGA | 7088 |
rs561812619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618619 | AAAACTAATACTAAC[A/G]AAAATCTGTTTTCTC | 7088 |
rs561826342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649716 | CATTTACTCTGCGCG[C/T]AGCTGCTGCTTGTAG | 7088 |
rs561841701 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669476 | AGCTGAAGTCTGGAA[C/T]GCAATTTTCCAGTCT | 7088 |
rs561865786 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690021 | CGTGGGGCTGGCTAG[A/G]GAGCGCGCGGGCGCG | 7088 |
rs561909231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619756 | CAGAGCCAATGGCCA[C/T]CTGGCTTGGTTTGGT | 7088 |
rs561938213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81594988 | GGACATAATCTCAAT[C/T]TGTTATCTGCTGGCA | 7088 |
rs561940087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681465 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 7088 |
rs561965825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588453 | AGGGTCACGCATGCC[A/G]GCCTCCTGACCTCAG | 7088 |
rs561971614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589022 | TGCAAGCCATCCCCA[A/G]CTTCTGCACTTTAGG | 7088 |
rs561975568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81595557 | GGCGCGGTGGCTCAC[G/T]CCTGTAATCCCAGCA | 7088 |
rs561986937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81667846 | AACCTGCAATGTTCC[A/G]CAACTCACTCTCAAA | 7088 |
rs562024001 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662873 | GTTGTTTTGAGACAG[A/G]GTCTCACCCTGTTGC | 7088 |
rs562042633 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584045 | TGATGGACTTGTCGC[C/T]TCCTCTTTGTAGACT | 7088 |
rs562063670 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689752 | CGGAGCGTATGGCAG[C/G]GCAGCGCCGGACGGG | 7088 |
rs562076124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680887 | GACTTAGGGGGAAAA[A/C]AAATCTCAAAGTGAG | 7088 |
rs562077595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81625639 | AGTAGGTGGGTTGAC[G/T]GAACCTCAGAGAGCA | 7088 |
rs562086517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626345 | CAATTAGGTAACGAC[A/G]CACCCCATCACATCT | 7088 |
rs562095313 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81663684 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 7088 |
rs562095448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657121 | TTTTCATGTATTTAT[C/T]GCTCCACTCTATGTT | 7088 |
rs562149555 | in-del | -/GT | | | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689660 | CCGGGAGGTTGGGGG[-/GT]GGGGGGGGGGCAGAA | 7088 |
rs562152980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675945 | ACCTCGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 7088 |
rs562160835 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81632225 | TAATTTTTTGTCCCC[A/C]CAATCCCCTCTCAAC | 7088 |
rs562199901 | snp | A/G | 0.000350898 | 0.0132411 | intron-variant | TLE1 | GRCh38.p7 | 9:81600076 | CTCTATCAATTACAC[A/G]TTTCCAAACTTCTCA | 7088 |
rs562228757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644707 | GCTTTAAAAAAGACG[A/G]ATTTGGCCAGGTGCA | 7088 |
rs562240086 | in-del | -/ATTAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629302 | GCAATTTATCCTTAA[-/ATTAA]TTAAAATATCTAAAG | 7088 |
rs562326139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673339 | TCTCCTTTTAAGCCT[A/G]AAGATAAATGCTTAT | 7088 |
rs562334922 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81597051 | CTGTTAAATGAACCT[C/G]TCTCTGGTTCTCTGG | 7088 |
rs562335041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683918 | ACATGATAAAGAAGA[G/T]GTCATCCCGCCACAT | 7088 |
rs562338393 | snp | A/G | | | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590222 | TGAGGAGAGACACAT[A/G]GGTACCAGAACTGCA | 7088 |
rs562363630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597320 | TTGAATTGAGGGCTT[G/T]ATCTCAACCAGTGGA | 7088 |
rs562389754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638438 | CTCCAAAAGGACAGC[C/G]CTCCTCTGTCCCATC | 7088 |
rs562425803 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81645116 | AGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGCA | 7088 |
rs562456973 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687524 | AAGAACGGGTGGGAC[-/AT]AAACATAAAGTTAGA | 7088 |
rs562464357 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680943 | TTAAAAAAAAAAAAC[A/G]AAAAAAACACTAAGG | 7088 |
rs562476439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81683201 | TAAAGCTCTCTGTAC[A/G]GAAAGTTTCCCCATC | 7088 |
rs562500042 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674689 | AAAGAGAGGAGGACT[C/T]TGTAAGGGGAGTCCA | 7088 |
rs562533382 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588344 | CACAGCAATGCCCTA[C/T]GTGCCAACAGAGCAT | 7088 |
rs562625562 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626381 | CCTTCTCCATCTACA[C/G]CTGGTGTCAATCAAG | 7088 |
rs562630178 | snp | A/G | 0 | 0 | intron-variant | TLE1 | GRCh38.p7 | 9:81641982 | AGCGGAGATCGCGCC[A/G]TTGCACTCCAGCCTG | 7088 |
rs562662157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643329 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 7088 |
rs562664682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647587 | CCAGGACTTGACCAA[C/G]TGGACCCACAGATCT | 7088 |
rs562688039 | snp | G/T | | | missense | TLE1 | GRCh38.p7 | 9:81610267 | AGGAATGGTAGGTAC[G/T]CTCATGTGAGGGGGA | 7088 |
rs562708468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678348 | CACTAGTACTAGCTA[A/G]TACTACAGGTCTGTA | 7088 |
rs562721319 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81610967 | ACAGCCTCTCCTACA[A/C]GTGCAATATCAGGAA | 7088 |
rs562732006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81598445 | TAACCTCTCTAATAG[G/T]ACTTCTCATATGGTG | 7088 |
rs562760422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611603 | GAAAGCTGACAAGAG[G/T]AAGGTGAGTGTGTGG | 7088 |
rs562783294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646922 | ACCAATAAACAGATT[C/G]CCATATAAGCCCCAT | 7088 |
rs562795826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605128 | GTCTGCCTCACCCAA[A/G]CATTCTTTCCGTGGG | 7088 |
rs562796720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81641557 | AATAAGAGTTAACAT[C/T]CAAAAAACTCAATAG | 7088 |
rs562822684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648888 | TCAAATGAGTAAGTT[C/G]CCCTCCCACAATGCG | 7088 |
rs562867757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81679777 | AATGGGGAGGGGAGA[A/G]GGTAGGAAACGAAAT | 7088 |
rs562885850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81616553 | AGAGGTCCCCCCACC[A/G]AGGGGCTCTACTTCC | 7088 |
rs562897922 | snp | C/G/T | 6.58924e-05 | 0.0057395 | missense | TLE1 | GRCh38.p7 | 9:81593087 | TGTCCCAGACCTTGA[C/G/T]GCAGCCCTTCCCGCC | 7088 |
rs562900907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639652 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAACCTC | 7088 |
rs562913698 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631824 | AGATGACTATCTCAC[C/T]GGGCATGGTGGCTCA | 7088 |
rs562962718 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689355 | GGGCCAGCGGGGGTT[C/T]TGGTCGCCGCGGGAC | 7088 |
rs562986988 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81655103 | GGGTGCGGTGGCTCG[C/T]GCCTGTAATCCCAGC | 7088 |
rs563031072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645288 | AGAATCGCTTAACCC[A/G]GGAGGCAGAGGTTGC | 7088 |
rs563060062 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689002 | CCTCCGGGCCCGACG[A/G]GGCTACTCCACCGAG | 7088 |
rs563067259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645689 | AGGCTGTGGTGAGCT[C/G]AGATCAAGCCACTGC | 7088 |
rs563094965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81684812 | AAAGTGAATGTCAGC[A/G]TATCTCCAGAATACT | 7088 |
rs563110575 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613325 | AACAGACAACAAATC[-/A]AGCTGGGAATGGGAG | 7088 |
rs563133614 | in-del | -/A | 0.00177266 | 0.0297184 | intron-variant | TLE1 | GRCh38.p7 | 9:81594352 | TACTATGCAGCCATA[-/A]AAAAAAAGGATGAGT | 7088 |
rs563143048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648244 | CACCACTGCACTCCA[G/T]CCTGGGTTACAGAGT | 7088 |
rs563146256 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81660353 | TCACAAAAAAAAAAA[A/C]ACAAAATCATACGTT | 7088 |
rs563176494 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682879 | ACCATGAAAGACTTA[A/C]GTATCTATTACCATT | 7088 |
rs563178684 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81655915 | TACAATCAAGCATAT[A/G]AAAAACAGCAGCCTT | 7088 |
rs563196230 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651741 | GGAAAGTATTTAAAA[C/T]TCTAACCTAAAGCTT | 7088 |
rs563235345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81625561 | TCTTTTAAAATAAAA[C/T]AAAACTAAACATTCC | 7088 |
rs563258702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81601658 | TACCAATGATCTCCA[C/T]AGAGCTCAGGGGAAT | 7088 |
rs563269087 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638224 | CTCAATGCCTGTCCT[A/C]CATCTGCAAAAGGAC | 7088 |
rs563278349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682553 | AAAATAAGGTTTATG[C/T]GTGCATTTACAGTAC | 7088 |
rs563362849 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688138 | CGCCGGGCCTCAGAA[A/G]CCACCAGTCTCCCTA | 7088 |
rs563401075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687507 | AGTAAGTCAGAGAAG[A/G]CAAGAACGGGTGGGA | 7088 |
rs563413525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81664938 | AACATGCTTTGAGAA[A/G]CACTGCCATCTATTT | 7088 |
rs563426607 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691361 | CATCACTCCCAAATA[C/T]CAATTATAAATGAAA | 7088 |
rs563441501 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81608190 | AAGGCAGGAGGACTG[C/T]GTGAAGCCAGGGCCT | 7088 |
rs563489819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687161 | GGAGACAAGAGAAGA[A/G]GCGGCCCGGGAAGAA | 7088 |
rs563506110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613763 | TTCTTCCTCCGCAGA[G/T]TTTATTTTAAAAGTA | 7088 |
rs563515291 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81609257 | GCCCAGCTAATTTTT[G/T]TATTTTTAGTAGAGA | 7088 |
rs563545275 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657608 | ATTAAAGTTATCAAA[A/T]ATAAAATAAAGAAAA | 7088 |
rs563572853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664527 | AAATATAATTATGCC[A/G]ATAAAATAACTAATC | 7088 |
rs563653892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615215 | GTGCCTGTAATCCCA[G/T]CTACTGGGGAGGCTG | 7088 |
rs563720092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609806 | TAAAGAGATGACACA[C/T]TTCAAAAAAGTGTCT | 7088 |
rs563752668 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689972 | AAGGTCGGTGGGAAG[A/G]AGAGCGGCGGGGCTG | 7088 |
rs563790160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589991 | ACTTCTGGAGCCCGT[C/T]CCTTCTCTGTGCAGC | 7088 |
rs563790701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81668342 | GAAATCTGGGATGCT[A/G]GCTAAATTTTTCAAA | 7088 |
rs563821909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81633018 | AGACTTAGAATGCAA[C/T]CATTAACACTTTTAA | 7088 |
rs563832681 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595604 | CGGGCGGATCACGAG[A/G]TCAGGAGATCAAGAC | 7088 |
rs563885848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671516 | AGGGCGTGGTGGCAT[A/G]TGCCTGTAATCCCAG | 7088 |
rs563929434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596427 | GATGGGCCTTTAGGA[C/G]GGATCAACTGGAAGG | 7088 |
rs563973324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677112 | CCGTGGTGGCACGTG[C/T]CTGTAGTCCCAGCTA | 7088 |
rs563993565 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615278 | AGGTTGCAGTGTGCC[A/G]AGATCACGCCACTGC | 7088 |
rs564037815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81617822 | CGAGGTCAGGAGCTC[A/G]AGACCAGCCTGGACA | 7088 |
rs564038183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661584 | GATCTTCTGGTTTCT[C/T]TGAACCAAGCGGGAA | 7088 |
rs564044507 | snp | C/G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648437 | GTGGAATGTGGGTTA[C/G/T]CAGGTATACACAGGT | 7088 |
rs564075122 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599150 | ATGAAGCGCAATATA[A/G]TCAACCTTTGTTTGC | 7088 |
rs564079378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611648 | GTCTTTGTCTCCGAG[C/G]TGTGTGGGGCTGGCT | 7088 |
rs564120571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592955 | GAATAAAACCCAGGC[A/C]CACACAGCTATTTCC | 7088 |
rs564189215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81679690 | ACTTAAAAACCACTA[C/T]ACTAAATACCCTGTA | 7088 |
rs564202554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617469 | TTGGGAGGCCGAGGC[A/G]GGCAGGTGGATCGCT | 7088 |
rs564242299 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650116 | AGCTAACCTGCCTTT[A/G]TAATAACCTCCACAA | 7088 |
rs564296369 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628959 | CCATGAATGCCACTG[C/T]GTAGGTCTATACACC | 7088 |
rs564301696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587439 | AACTCATATGTAAAT[A/G]TAACAGAGAACACAC | 7088 |
rs564333921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686624 | TCTGAGTTAGAATCA[A/G]GTAAAACTTCATAGG | 7088 |
rs564340453 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81624034 | CAGCCAAAGTGCCTC[C/T]CCTCTCAGAAGAGTG | 7088 |
rs564363035 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81592314 | AGTGAGCCGAGATCC[A/G]GCCACTGCACTCCAG | 7088 |
rs564366965 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672183 | TGGCACAACTTGTCT[C/G]AACTGTGCCCTGCTT | 7088 |
rs564382282 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642881 | TACCTATAAACACAA[C/T]GGAATACCATTCAGC | 7088 |
rs564391423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675273 | CTTTTATTCTGTAAT[C/T]TGAAATTTTTCATAA | 7088 |
rs564451264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81669379 | TCCGTGGCACAAGCC[A/G]GGAACCAGTTAAACA | 7088 |
rs564454189 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669719 | GTCCAATTAAAGCTG[C/T]TTAATCATTATTTAG | 7088 |
rs564458978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632144 | AAAACAATAAGGCTT[C/T]CTCCATAAACTAAAG | 7088 |
rs564466168 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690385 | ATGAGCAACGCCACG[A/G]TTGGCGTAGGTACAC | 7088 |
rs564467151 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603238 | GTGTCATAGGCTTTC[C/T]AGGACACTGTTCCTC | 7088 |
rs564470892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686126 | GCCTATCTGGTTAGA[G/T]GACAAGAATGAAAAA | 7088 |
rs564483565 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81675890 | ATTTTCAGCAGAGAC[A/G]GGGTTTCACCATGTT | 7088 |
rs564493584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628291 | TTATAGATGGGACTA[C/G]GAAGGCACAAAAGGA | 7088 |
rs564536058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589490 | ATTTGTAAGACGCTA[C/T]CCCATTCTATCCAAC | 7088 |
rs564560247 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81683133 | TCCGACAAACCCGTT[C/G]AAAGGTGGGAAGGGA | 7088 |
rs564597903 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81597014 | GATTAGGTCCACAGG[C/T]AAATCAAGTGCCCAA | 7088 |
rs564630494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644668 | TACAGCAATGTGAAT[A/T]CGCTAAAAACCACAG | 7088 |
rs564662020 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81632719 | TGAAAACATGAACTC[-/TA]CGCACACAGCCCTGT | 7088 |
rs564673745 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81605902 | CTAATATCCAGAATC[C/T]ACAAAGAACTTAAAC | 7088 |
rs564696211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680440 | ACAAAATTTGGACAT[A/G]TTGTTCCTTGAAGAT | 7088 |
rs564754682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649712 | GCTGCATTTACTCTG[C/T]GCGCAGCTGCTGCTT | 7088 |
rs564759837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603143 | TCAGCCCCTTCCCCT[A/C]TTGGGTTAGTGCAGC | 7088 |
rs564793395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81650029 | AGTATGCCCAAGACA[C/T]ACAATGGGCCTAAGT | 7088 |
rs564861961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687942 | TCGGGGAAGGTAGAG[A/G]GGATATGGCTGCAGG | 7088 |
rs564884205 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81609233 | GGGATTACAGGCACA[C/T]ACCACCACGCCCAGC | 7088 |
rs564910011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665158 | ACATTTTTACAAAAC[A/C]CTGAGGCAAGAACAC | 7088 |
rs564911398 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81673004 | AAGGCCGGACGCGGT[C/G]GCTCACGCCTGTAAT | 7088 |
rs564933685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81670475 | GGACTACAGGCGTGC[A/G]CCACTGTGCCCAGCT | 7088 |
rs564956737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677677 | TAACCTACTTAGATC[A/C]GTCATGGTGCTAATA | 7088 |
rs564973263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81641500 | AAAATGATGCATGGG[A/C]AACCTAAGGAATGGG | 7088 |
rs564974352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81640710 | CAGCTTGGGTCAATT[A/G]TATTACTATAATGAA | 7088 |
rs565040837 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81648165 | TAATCCCAGCTACTC[A/G/T]GGCGGCTGAGGCAGG | 7088 |
rs565059399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81642157 | TTAGGAATGTAAATT[A/G]GTACAGCCCTGATGC | 7088 |
rs565076474 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81677292 | CAACTCAGGCCGGGC[A/G]CAGTGGCTCACACCT | 7088 |
rs565092228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683135 | CGACAAACCCGTTGA[A/T]AGGTGGGAAGGGAGA | 7088 |
rs565137221 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81685244 | GATAGTCATATACCT[A/T]GATTACCACGATTAA | 7088 |
rs565139101 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603634 | TCTCTTAGTTACTTC[C/T]CCACAATTTACTGCC | 7088 |
rs565216013 | snp | C/T | | | missense | TLE1 | GRCh38.p7 | 9:81585628 | CTGCCAGCCACTCCC[C/T]GGTGGGGCAGTACCC | 7088 |
rs565260728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597404 | AGGAAAGCACAAGGG[C/T]AGTGATGAGGCAACA | 7088 |
rs565265785 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | TLE1 | GRCh38.p7 | 9:81684149 | CCTTCAGAGTAAATT[A/T]AAAAAAAAAAAAAAG | 7088 |
rs565265949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622272 | GCAGGGCTGTATCTT[A/C]TTCAACTTTAAATCC | 7088 |
rs565283970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610888 | CCCTACTTTGTGCAG[C/T]GTTAAGGACAGCATG | 7088 |
rs565300153 | in-del | -/GCAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610572 | ACTTCCCTTAGACTT[-/GCAA]GCAAGTTCACAGAGC | 7088 |
rs565303991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597720 | AGAATAAAGCCCACT[C/T]GACTTCACAGATGTA | 7088 |
rs565347358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616515 | CATGAGCAACCATTA[A/C]CTTCTTAATGTAAGA | 7088 |
rs565410029 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688986 | CCGCGGTTGCACAAA[C/T]CCTCCGGGCCCGACG | 7088 |
rs565491662 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688480 | GGGCGCCCCAGGCCC[A/G]GCTGCTTCAAGAACC | 7088 |
rs565527460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649438 | TCCAGGTTTGATAAA[A/G]AGAAATATCTTTAGC | 7088 |
rs565548979 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81678013 | TTCTACCCAAAGTGA[C/T]TTGTATCCTACTCTT | 7088 |
rs565552405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665757 | GTGGGGCCCATCAAA[A/G]AATGACAAAGCAACT | 7088 |
rs565566274 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81649764 | GTACCTCCTCCCCTC[C/T]GGGGAGACAGGTTGA | 7088 |
rs565566832 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655496 | AGCCCAGGGAAGGGT[A/C]CACCTGCAGCACCTC | 7088 |
rs565592793 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656168 | CAGCTGTACCAGGTA[C/T]AAAAACAGAACTGGG | 7088 |
rs565602051 | in-del | -/CTCT | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81625171 | TAAGAAGGGACTGGA[-/CTCT]CTCTCTCACGAAAAT | 7088 |
rs565603363 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81644391 | AATTGTCAATAAAAA[C/G]GACTAAAATACTGGT | 7088 |
rs565641923 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81637989 | GATTTCTCCTGTAAC[A/C]CCAGCAGCTCAATCA | 7088 |
rs565693362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81595128 | GGAATAAATACACAT[A/G]TAAAAACAATATAGC | 7088 |
rs565711793 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81638625 | AATCAGGAGAATTTA[C/T]GCACACTTTTCTTTT | 7088 |
rs565720295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631580 | TCGAATTGCAGATGC[A/G]TGTCCCATAATGCCT | 7088 |
rs565743436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81601219 | ATCAGAAACAGAAAA[A/C]GTGGGGTGAAAGGGG | 7088 |
rs565811601 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690886 | GTGGAACTTGAGTTA[A/C]AAGGGATTTTGAGAT | 7088 |
rs565826653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617558 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCGCA | 7088 |
rs565841327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | TLE1 | GRCh38.p7 | 9:81612350 | TTTCTCTTTCAGTCC[A/G]AACTTTCCATTCCCT | 7088 |
rs565879796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599195 | GGGCTCACTATCCCT[C/T]ACTGTTTAGAGATGA | 7088 |
rs565891271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687226 | ACTGAGACTCCACAC[A/G]CCACCGCCTGGACGC | 7088 |
rs565891589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81606210 | TTGTGGAAGACAGCA[C/T]GGCAATTCCTCAAGG | 7088 |
rs565893813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643979 | CTACAAAAACTATAC[A/T]GGTTTTGATTGAAAA | 7088 |
rs565931295 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583642 | CATTGATGATCCCAA[A/G]GCTTTAATAAAAAAC | 7088 |
rs565958396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681942 | TGATGGCAGCATGAG[C/G]GGATAGGAAGAAGCA | 7088 |
rs565995221 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663917 | GTGTGAGCCACCACA[C/G]CTGGCCAGAATAGAC | 7088 |
rs565996001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669500 | CCAGTCTGCAAGCAG[C/T]ACTGTAAAGTAGAAA | 7088 |
rs566078541 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687631 | CCCGGCTTCTAAAGA[C/G]GCTCGGAAGCTCTTC | 7088 |
rs566090752 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TLE1 | GRCh38.p7 | 9:81607357 | ACACACACACACACA[C/T]ATAAGGAATAGGGTC | 7088 |
rs566109924 | in-del | -/TAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618906 | CTGTCATCAGTGATC[-/TAA]TAAGGTCTGAGGCCT | 7088 |
rs566139681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657267 | CAACCTTGCTTAATA[C/T]GATTTTTTTGCTGTA | 7088 |
rs566163518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644248 | ATCCAAGAGAAAACA[G/T]GCCCACACAAAAACC | 7088 |
rs566193815 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641657 | AAGAAGACACACAAA[C/T]GGCCAACAGATATAC | 7088 |
rs566199044 | snp | A/G | 3.29516e-05 | 0.00405891 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81613468 | CGGCGTTGGCATGTC[A/G]CTCCGAGGCGTTGGT | 7088 |
rs566299061 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81675487 | TCAATTCACACCAAA[-/C]CTAGGCCCCAGCAAC | 7088 |
rs566300048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663097 | ATTATCCACACGCCT[C/T]GGCCCCCCAAAGTGC | 7088 |
rs566320511 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589323 | TCTGCCCTCTCTCCG[C/T]CCATATACTATACTC | 7088 |
rs566321283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586261 | TGACTTTGTGATCCA[A/C]CCGCCTCGGCCTCCC | 7088 |
rs566356760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81624638 | GCCAAGAAACCCAAA[C/G]TTTTATTTCACCTTG | 7088 |
rs566356788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631961 | TACAAAATTAGCCAG[A/G]TGTGGTGGCACAGGC | 7088 |
rs566360341 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689029 | CGAGAGCAGTCCCGC[A/G]AGTGCCCAATGCTCC | 7088 |
rs566383993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81585715 | CTTAGGAAGGGAAGA[C/T]GCAATGTGAAAAGTG | 7088 |
rs566481614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81623774 | CAGCCTGGGTGACAG[A/G]GTGAGACTCTGCCTC | 7088 |
rs566523090 | snp | C/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690322 | TGAGCTGCCTTTTTA[C/G]GGATGTACGAGAGGG | 7088 |
rs566562205 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81666168 | TCCCAGGATGGAAAA[A/T]GGACAGCTTTTGGTG | 7088 |
rs566582598 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667942 | GCTGAGGAGGGTGGA[C/T]TGCCTGAGGCCAAGA | 7088 |
rs566635631 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81665437 | CTGAGCTCTCTCCAA[A/C]TGGGCCCAGATACTA | 7088 |
rs566659368 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597756 | TGAATGATATAAAAA[C/T]CCATTAAGAGCAAGG | 7088 |
rs566667055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629610 | TAAGAAAGCCATGTC[A/C]GGCAATTTCATCATT | 7088 |
rs566750507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81627614 | CAGGAGTCTGCTTAA[C/G]AAAACCTAAGTGTTT | 7088 |
rs566765308 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TLE1 | GRCh38.p7 | 9:81661163 | TAAAAATAAAAAATA[C/T]ATATATATTTATATA | 7088 |
rs566766452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81636490 | CATACACAAGCAAGT[A/G]CAGCGGGTAATTAAG | 7088 |
rs566787436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628414 | TTCCCATAGGCCTCC[A/G]GGAATGAACGTGATT | 7088 |
rs566794121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672555 | AGCCCATGGAGTAGA[C/G]GAAGAAAGACAGCAC | 7088 |
rs566858003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81660576 | CTGCTACCACACCCG[C/G]CTAATTTTTTTTTGT | 7088 |
rs566859195 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583832 | CTGCTCTACAAAGGA[C/T]GGAAAGTGAGGTGAA | 7088 |
rs566920557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81667171 | CAATTCCAGCATTTC[A/G]GGAGGCCGAGGCAGG | 7088 |
rs566950557 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647194 | TTTTGTGGACGGGAG[A/G]ACAGTCCCCACTGGT | 7088 |
rs567060516 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81679184 | AATAATGAAACATGT[A/C]ATTTTGCTAAATCAC | 7088 |
rs567079691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684876 | AATGACTACTCAATC[A/G]AGGGTCCTTTGGGCT | 7088 |
rs567096780 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687984 | AGCCTTCCCCAGCGC[C/T]CCTGTCCGCTCGGTA | 7088 |
rs567121162 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81642458 | AGCCTTTGGGAGGCC[A/G]AGGAAGGTGGATCAC | 7088 |
rs567128346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663284 | ACCCAGCCCTCTTAC[A/G]ATCCTCAAATCACAG | 7088 |
rs567132012 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81648286 | CAAAAAAAAAAAAAA[C/T]CCAAGCATCTTTAGC | 7088 |
rs567159605 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81669036 | ACCAAATTTAACCCA[C/T]GTATTCTGTTACACT | 7088 |
rs567202592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597520 | AGATGGACGTTTGGA[C/T]AGAATCGTGGCAAAC | 7088 |
rs567224277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638905 | GCTGAGATTACAAGC[A/G]TGCGCCACCACACCA | 7088 |
rs567262694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626081 | AAGGAAAACCCATTC[A/G]TGCATACAGCAAAAG | 7088 |
rs567283692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677428 | AAATTAGCCGGGCAT[C/T]GTGGCAGACGCCTGT | 7088 |
rs567285008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81670453 | GCCTCAGCCTCCCTA[A/G]TAGCTGGGACTACAG | 7088 |
rs567320684 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604099 | AGACTCCCATGTACA[C/T]CTAAATTCTTAATAA | 7088 |
rs567324581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589790 | AAGTAACTTTTGCTA[A/G]GATAAAAGGTGGAGA | 7088 |
rs567325546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81595377 | CTATTCATGTCCTAC[A/C]AGAATTCTAGGCTTT | 7088 |
rs567339026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591290 | CTGCATCACAGAGCT[C/G]AAACTATCTAGGTAT | 7088 |
rs567347330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677865 | GATCAGCAAGCTACA[C/T]ATACAACTCTATCCC | 7088 |
rs567360300 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81682073 | AACATGGGTGAAACC[-/CT]CTCTCTACTACAAAA | 7088 |
rs567388592 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81607530 | TGAAGCTAGCTTTTT[-/C]CCTAAGGATCAGCTG | 7088 |
rs567415619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81644881 | TGCCTGTAATCCCAA[C/T]TACTCGGGAGGCTGA | 7088 |
rs567468334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81595679 | AAAAAATCAGCCGGG[C/T]ATGGTGGCGGGCGCT | 7088 |
rs567489925 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81600353 | TAAAGTGAGGAATTA[G/T]TATAGCTAAACACAA | 7088 |
rs567510198 | snp | G/T | 1.65581e-05 | 0.00287728 | intron-variant | TLE1 | GRCh38.p7 | 9:81652307 | TGAAAACAAGGAGAA[G/T]AAAGGGCATTAGCAA | 7088 |
rs567577937 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81671975 | AGCCAGCCCACTTAC[A/T]AATGGAAAAAGTTCT | 7088 |
rs567586035 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634796 | TATAGTAGCCATACT[C/T]TCAACCTGTCACCAG | 7088 |
rs567599431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687185 | GGAAGAACCAGGAAA[A/G]GGGGTAACTTGAATG | 7088 |
rs567611306 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81681170 | GAAATATCACATGGA[A/G]CTCTTTCCCTTTCCC | 7088 |
rs567674653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686198 | TGCTCCCTACCTTCC[C/T]GCATCAGTTTGTTTC | 7088 |
rs567674739 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656579 | GTGATTTTAGGATAC[C/G]ATCATTCCAGGTTCT | 7088 |
rs567680438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680049 | GAACATCTTAAGTCC[C/T]CTGGCGAAGGACGCT | 7088 |
rs567717720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646417 | AAATACAAGTTAGTA[C/G]AGCTAGAAGATCCAT | 7088 |
rs567735505 | snp | A/C/G | 5.06371e-05 | 0.00503155 | intron-variant | TLE1 | GRCh38.p7 | 9:81593325 | ACATTTACAGAGGAA[A/C/G]CAATCCCTATCTCGG | 7088 |
rs567737489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680470 | TTTTGGGGGCATTCC[A/G]TTTGAATTTTCAAAA | 7088 |
rs567758796 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674856 | GGTGAAGACAGAATT[C/G]TTAAAATGTACATGG | 7088 |
rs567787186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602710 | CACATGGACCTGATA[A/C]GTGCTTTACAATAAA | 7088 |
rs567833453 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | TLE1 | GRCh38.p7 | 9:81608944 | CCGTCTCAAAAATAA[A/T]AAAAAAAAGAAAGAA | 7088 |
rs567846961 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611632 | GGCTGGGAGACTGGG[C/T]GTCTTTGTCTCCGAG | 7088 |
rs567883165 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646599 | CTCTTAAACTTCACA[C/T]ACTACAATCCCATAG | 7088 |
rs567936212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81620711 | ACTTTGATGGCAAAC[A/G]TATCTACAGGTTTAC | 7088 |
rs567939079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599003 | TGACCAGTAACATGT[A/G]GGCACCAAGCCTAAC | 7088 |
rs567970189 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81660568 | ACAGGTGCCTGCTAC[A/C]ACACCCGGCTAATTT | 7088 |
rs567997739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614140 | GTCTCGATCTCCTGA[C/G]CTCGTGATCCACCCG | 7088 |
rs568044468 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689645 | GCGGGGGACGTGAGC[A/C]CGGGAGGTTGGGGGG | 7088 |
rs568065912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599590 | CTCATAAGAAAATCA[A/G]TCTTATTATTCTAAG | 7088 |
rs568071779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674398 | CTCCTGAGGAGCAAC[C/T]GGAAGGCCACAGCAT | 7088 |
rs568077610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81612931 | GGCGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 7088 |
rs568094499 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81644262 | ATGCCCACACAAAAA[C/T]CTGTACACAAATGTT | 7088 |
rs568213129 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81635970 | TTGAGACCAGCCTGG[A/G]CAACATAGGGAGATT | 7088 |
rs568216277 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689172 | TCCTTCCTTCACCTT[C/T]GTGTGCTTCTCCGCA | 7088 |
rs568223155 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81612611 | CAGAAAACCAGCAAA[C/G]TATAGTCTGCAAGGA | 7088 |
rs568239854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612512 | CAGGTTGCAAATTAT[G/T]AGTTTTTTAAGGGCT | 7088 |
rs568239976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655036 | CTGAACATAATAAAA[A/G]GTGTCCTTAGTGTCT | 7088 |
rs568339062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81637098 | GAAGGTGGGTCATGC[C/T]TGTAATCCCAGCACT | 7088 |
rs568369106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588199 | AACACACAAAATCCC[A/G]ATTGTATTCCTTATG | 7088 |
rs568370922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81594208 | GACTGGTGCTCCTAC[A/G]GCCCCTCTGGGCCAC | 7088 |
rs568390888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617013 | AGCTCAGTAAATGGT[G/T]GCAACAGCTGAATTT | 7088 |
rs568394272 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81650776 | TTATGCAGAGCTAAG[C/T]TGTCAAGTGTAATAA | 7088 |
rs568435799 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598156 | TCAAAAACCTTCATT[C/T]GCTCTTCAAGCTCTT | 7088 |
rs568457194 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643266 | TTTTTGACAGAGTTT[C/T]GCTCTCGTTGCCCAG | 7088 |
rs568469652 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621781 | GGGAGGGTTGTCTCC[A/G]GCTCAACCATATGCA | 7088 |
rs568478993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615409 | TGTGGCAAGAACATA[A/T]CCCCCAAGTAAGACG | 7088 |
rs568504859 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583557 | AGCCTACCACCAAAT[A/G]TATTTATAAAATAAG | 7088 |
rs568511646 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594367 | AAAAAAAAGGATGAG[C/T]TCATGTCCCTTGCAG | 7088 |
rs568521632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81662494 | TGAGGTCAGGAGTTC[A/G]AGACCATCCTGGCCA | 7088 |
rs568557203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81668884 | GAAGTTACCACTCCT[A/G]TAATTCACAAGTTAT | 7088 |
rs568608797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621437 | TTGTTCAGTGATGTG[G/T]TACTGCCCTGAACAA | 7088 |
rs568637678 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664252 | GACACTGCCTCTACC[-/A]AAAAAAAAAAAAAAC | 7088 |
rs568638778 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81614995 | AGGTCAGGAGTTCAA[C/G]ACCAGCATGGCCAAC | 7088 |
rs568673964 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641774 | ACGCCTGTAATCCCA[C/G]CACTTTGGGAGGCCG | 7088 |
rs568702376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591185 | AGAGCAAGAGTTCTC[C/T]AGTCAAGATTGGGGT | 7088 |
rs568714253 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81631069 | TAGAACTTGTCAAAA[A/T]TTTGATATAAAAAAG | 7088 |
rs568763917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590421 | TGTTATCTTTTATCA[A/G]TTGGCTCTTGTCTGC | 7088 |
rs568838764 | snp | A/G | 1.90478e-05 | 0.00308602 | intron-variant | TLE1 | GRCh38.p7 | 9:81610197 | CACCTTTAAAACAAA[A/G]CCAAGGTCTTTGAGG | 7088 |
rs568857519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628392 | ACCACCCCTGATGCC[A/G]CCATGGTTCCCATAG | 7088 |
rs568871437 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625091 | GCAGAACTGGCATAA[C/T]TTTTATATAGAAAGT | 7088 |
rs568890625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81666485 | TTATGAAACTAAAAT[A/G]TGCCTGTGTAGCCAG | 7088 |
rs568920444 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684223 | TGACGATAGATGTTA[A/G]CCACAGATCTTCTAG | 7088 |
rs568929773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665336 | TTTAGTGGCTCAACT[A/G]ATCAGAACACAAGTC | 7088 |
rs568933883 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670514 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATAT | 7088 |
rs568941838 | in-del | -/GAATG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644361 | AAGCAACTGCAGTAT[-/GAATG]ATTGATGAAATGTTA | 7088 |
rs568956011 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81646797 | CCCTACACAAAAACA[A/T]CTAGTCAGACATCAC | 7088 |
rs568964692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672491 | TTGCTTCCCCAAATA[C/T]TAGTACATCAGCAGC | 7088 |
rs568994501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586086 | GAAGCGGCGTTATCT[C/T]GGCTCACTGCAAGCT | 7088 |
rs568997703 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673205 | TTGAACCTGGGAGGT[A/G]GAGGTTGCAGTGAAC | 7088 |
rs569027532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671822 | AGTTCCCCTCCTAAG[C/T]TAGTGGTATGATTTT | 7088 |
rs569044338 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81633311 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGC | 7088 |
rs569056656 | snp | C/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690624 | TTCGTCTTAAAAGTC[C/T]TGACTTCGCTGTGTT | 7088 |
rs569116204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81630228 | GTCCCGGAGACCCTC[A/G]CAAATCTATGAGGGC | 7088 |
rs569155548 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81642253 | ATCCCTTTTCTGAAG[G/T]GCTTGGGACCAGCAA | 7088 |
rs569162459 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81671084 | AGACAGGAGAATAGC[-/T]TTGAACCTGGGAGGC | 7088 |
rs569164224 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81677360 | CATGAGGTCAGGAGA[C/T]CGAGACCATCCTGGC | 7088 |
rs569194985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622593 | CTTTGAGGCCTCTGC[G/T]TCTATGTGTTCAAAG | 7088 |
rs569219469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81641796 | GGGAGGCCGAGGTGG[A/G]CGGATCACCTGAGTT | 7088 |
rs569224116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586977 | GGTAAAAAATAAATG[C/T]CAAGTCATGATCGAA | 7088 |
rs569303547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669590 | TGTACATGCAAATAT[A/G]TGCATGCTTACACCT | 7088 |
rs569315947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81670365 | GAGTCTGGGTCTGTC[A/G]CCCAGGCTGGAGTGC | 7088 |
rs569321373 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81619614 | AAGGGCATCAGGGAC[A/G]TAGCCCCATTTCAGC | 7088 |
rs569330052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662627 | AGCTTGAACCCATGA[A/G]GCAGAGGTTGCAGTG | 7088 |
rs569367253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673165 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAA | 7088 |
rs569396727 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612680 | TTAGCAAAGTCAGAC[A/G]CACAATGCTAGTTAG | 7088 |
rs569431437 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81684248 | TTCTAGCCCATTTAC[C/T]ATCAAGAAGTTACAA | 7088 |
rs569432115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639360 | GTAAGCTACCATAGC[C/T]GGCCTGCATCTGTAC | 7088 |
rs569447976 | snp | A/C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627409 | TCCCACCAAGGCCCC[A/C/G]ATATCCACCTGACTT | 7088 |
rs569453346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678587 | TGGGAGGCTGAGGCA[C/T]GTGGCTCACTTGAAA | 7088 |
rs569492408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81610660 | CAGTTCTTTTCTTTG[G/T]TAGGGGCCGTCCTGG | 7088 |
rs569499408 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688534 | GGGACTGTGCGCGGG[A/G]GCAGCGCTCCAACCC | 7088 |
rs569504850 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81647217 | CCACTGGTCATCTGA[C/T]GATGTCTTCTAACTC | 7088 |
rs569509335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81625157 | AACCATATACTCCAT[A/G]AGAAGGGACTGGACT | 7088 |
rs569559384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644793 | GAGGTCAGGAGTTTG[A/G]GAACAGCCTGGCCAA | 7088 |
rs569573025 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583746 | TTATACAAATGTTTA[A/C]CCTTCAACAAAAATA | 7088 |
rs569590913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632341 | GATACATGAAATATA[C/T]CAAGATCTGTCTCAA | 7088 |
rs569621400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81644504 | TCATATGAGATGTCC[A/G]GAATAGGCAAATTCA | 7088 |
rs569637477 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655094 | GGAAAGGCCGGGTGC[A/G]GTGGCTCGCGCCTGT | 7088 |
rs569652215 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TLE1 | GRCh38.p7 | 9:81595628 | TCAAGACCATCCTGG[C/G]TAACAGAGTGAAACC | 7088 |
rs569655581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589736 | TAGAATTGATATTTT[C/G]AAAGTGCTACTTATG | 7088 |
rs569673111 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687983 | CAGCCTTCCCCAGCG[A/C]CCCTGTCCGCTCGGT | 7088 |
rs569681502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675725 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 7088 |
rs569730611 | snp | A/G | | | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634104 | CCTCTCACCTCTGTG[A/G]TGCTCTGCATCGTGG | 7088 |
rs569745054 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611075 | GGACATTTTTCAAAC[A/G]GCCAAGAGAAATGAC | 7088 |
rs569761498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681549 | AACGAGATTCCGTCG[C/T]GCAAAAAAAAAAAAG | 7088 |
rs569771285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681122 | AAAAGCAGTTTCACT[A/C]CAAAATTTACATGGC | 7088 |
rs569780156 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588392 | CAACCTTGCTTTCTG[C/T]GTTAGAAAGAGCCCT | 7088 |
rs569786678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632316 | TTCCTCACTCCTCCA[C/T]GCACATCCAGATACA | 7088 |
rs569797540 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687282 | CACCCGGCTGGGTGC[A/G]AGGGGCACCGGGACG | 7088 |
rs569808244 | in-del | -/CCCTTTTTTTTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632473 | TTAAATGTTCAGTAT[-/CCCTTTTTTTTTT]TTTTTTTTTTTACCA | 7088 |
rs569821471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649800 | TGCATGTTCAATGAA[A/G]GGGTGCAAAGGTCCA | 7088 |
rs569846985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81599813 | TAACGGAGGGCTTTA[C/T]TAACAACTAACTTGA | 7088 |
rs569860921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687658 | CTTCCCAGTCTCCAG[A/G]GCGGATTGCGCTAAG | 7088 |
rs569894728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81606469 | AGTTCATGTCCTTTG[C/T]AGGGACATGGATGAA | 7088 |
rs569910215 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81663771 | AGCTGGGACTACAGG[C/G]ACCTGCCACCACGCC | 7088 |
rs569940326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81650675 | TGAATGTGATTAGAG[A/C]GCCCACTAAGTAACA | 7088 |
rs569950172 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690082 | CCGGGGAAGCTGAGG[C/G]CTCGAGTTAGCAAAA | 7088 |
rs569965939 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81602572 | CATGAGGTCAGGTGT[A/G]GAATTTTCCATGTGT | 7088 |
rs569969839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676906 | TTCATTTATTTTAAA[C/T]GTATACAACAGTGTA | 7088 |
rs569972413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663213 | GGCTCACCACGTTTG[C/T]GATCAACAGTGGTGC | 7088 |
rs569977409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612875 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 7088 |
rs570058404 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638933 | CAGCCGATACATGCA[-/T]TTTTTTTTGAAGCAA | 7088 |
rs570066935 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637487 | CAACAGTTTGACTAA[C/T]ATCTATCAACAGCAA | 7088 |
rs570067463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684905 | CTGAGCAATCATTTA[A/G]CTTTTCTTCTCTTAT | 7088 |
rs570085744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604805 | TCTCTCTCTGTGCAC[A/G]ACACAGACTGTGCCT | 7088 |
rs570110300 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646372 | ATAAAAGGGCTAGAG[A/T]GTTGGAATTTAAGTA | 7088 |
rs570114326 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81640074 | GCTACTGGTGCATCT[A/C]ATGGGTGAAGGCCAA | 7088 |
rs570121862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597985 | GGTTGTTGGTTTCCT[A/G]GAAATAGGAACTGCA | 7088 |
rs570143764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657354 | CCTTTAGGTAAAGAT[G/T]AGAACACATCAATAT | 7088 |
rs570170304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645962 | TTCTGAAGCTTTTTT[A/C]TCCTTCTGGAAAAAT | 7088 |
rs570178344 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660310 | CAACCAGATAAACCA[C/T]TACTAAACAGTGCTA | 7088 |
rs570190282 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688811 | TTCGGCTGCGCCTTC[A/G/T]GCCGGGTGCTCGCAG | 7088 |
rs570190902 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668095 | GCTTGAACCCAGGAG[A/G]CGGAGGTCGCGATGA | 7088 |
rs570229656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81613584 | ATATTACACAATTTA[C/T]CACAACAGCAGCTGG | 7088 |
rs570243156 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682026 | CAAGGTGGGTGGATC[A/G]CTTGAGGTCAGGAGT | 7088 |
rs570248899 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665786 | CTCTATTCATTGGTT[C/T]TCCTTCCTGCAATGA | 7088 |
rs570262641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81658072 | CGTGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 7088 |
rs570285784 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81596010 | AAGGCCAGGTTTCCA[G/T]GAGGCACCCTTTCAT | 7088 |
rs570304056 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684502 | ATTAAAAATCAAAGA[A/G]TGCGGAGTTACAAAA | 7088 |
rs570324867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81625890 | TACTAACATGTTCTG[C/G]AAAGTAACCTCAGAA | 7088 |
rs570396563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619952 | CTGCCTTGAGAAGTA[C/T]CATGAGCCTATATTA | 7088 |
rs570425059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655001 | ACTCAAAGACCTCAC[C/T]GACAGGGCCCAGGGG | 7088 |
rs570444010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81679262 | AAAAATATTACGGTG[A/G]CTGGGTAGTCTACAA | 7088 |
rs570448965 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616815 | AAAACTACCTGGGAC[A/C]GGCCTGCAGGCTCTC | 7088 |
rs570482480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618164 | TATACAATGTAGGCA[C/T]ATGGAAAAAGCAGGA | 7088 |
rs570486090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81611277 | CCTGTTTACAGAGAC[C/T]ACTGCTTATATATAA | 7088 |
rs570521379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81610750 | CATACCTGCCCCCCC[C/T]CCCACCCCCAGTTAT | 7088 |
rs570573273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648375 | AGAAGGGGAAAAACT[G/T]TAAGAATAATGGAAT | 7088 |
rs570590073 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81660477 | GGAGAGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 7088 |
rs570593998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81616247 | AGTCCTTCGGGTTGG[A/G]GTTGTACAAGGTGAC | 7088 |
rs570616756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586733 | CTCTGTGCTTTCATA[A/T]ATGCTTGGACATTTG | 7088 |
rs570622222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81660078 | AGAAAGCTTCCATAC[A/G]GTTTCTTAACAGCTT | 7088 |
rs570650719 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603091 | ACAGCGTGAAGTCAC[C/T]GGGCCTTTGCACATG | 7088 |
rs570753304 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81622003 | CACAGTGTTTGGGGA[C/T]GAAAGGTGAGCCGGC | 7088 |
rs570755088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629387 | GGTCATTTCATATTT[A/C]TCTGCTCAAGAGCTG | 7088 |
rs570790614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655969 | TAACTAAGCAAAGTC[G/T]TTGGTTTTATAAGAT | 7088 |
rs570845569 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624068 | TTTAAACTCAAGTTT[A/G]CATACATGGAACACT | 7088 |
rs570874482 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81666601 | CTAACATGACGAAAC[A/G]CAGTCTCTACTAAAA | 7088 |
rs570883017 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TLE1 | GRCh38.p7 | 9:81661201 | TTTTATATATATATG[C/T]ATTTTTATATATATA | 7088 |
rs570887083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588528 | GGCACCTCAGCAAGA[C/T]TCTGCCTCCAAGCGG | 7088 |
rs570949995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81674298 | TGCGTGTCAATACAC[C/T]GGCTGGCCACTGTAC | 7088 |
rs570978813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588104 | AACTTAAATATGCTA[C/T]TCTGACAAAACCGTC | 7088 |
rs571052744 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637806 | AGTGCTCCTAGATAA[C/T]ATCTAAGTGTCCATC | 7088 |
rs571085615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81679982 | TGATTTATTTAAATA[C/T]TTACTAAAGAAACAG | 7088 |
rs571112718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614323 | TAACCTTACCAATAT[A/G]CCTAAAAAGAACAAC | 7088 |
rs571171149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592599 | TTAAAAACACAGACC[C/T]TGTTCAGAATGGTTT | 7088 |
rs571277009 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674869 | TTCTTAAAATGTACA[G/T]GGACGCCAGGTGTGG | 7088 |
rs571288939 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629797 | CTAAACATAGAAAAG[A/G]TACAGTAAAAATACG | 7088 |
rs571311356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673135 | AAAATCAGCTGGGCA[A/T]GGTGGTGCACGCCTG | 7088 |
rs571328974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665526 | GAAAGGAAGGAAAAA[A/G]AAAACCGTGCTGAAG | 7088 |
rs571329689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671683 | TATATACTCAGAAAA[A/C]TCCAGTCAGTATTTG | 7088 |
rs571340541 | snp | G/T | 0 | 0 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589846 | TCCATTTTGCTCACC[G/T]ACACTACCCAGCAAA | 7088 |
rs571381497 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627626 | AAGAAAACCTAAGTG[-/T]TTTTCCATTGTGCCC | 7088 |
rs571407275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596120 | GATTAAATAGATGCA[C/T]CGAGTAACAGACGGG | 7088 |
rs571435749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81639543 | AACATAGAACACACA[G/T]GCAAAAGTTTGTAAA | 7088 |
rs571456832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676806 | GCCAGGTTTGACATA[C/T]GGGCTAGCAGTCTCT | 7088 |
rs571469301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671255 | ATGGTAGCAAATGCC[C/T]GTAATCCCAGCACTT | 7088 |
rs571519387 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600603 | AGGAACAAAATGGGC[A/C]TGTTATTTTTAGCAT | 7088 |
rs571527395 | in-del | -/AAAAAG | 0.0573587 | 0.15934 | intron-variant | TLE1 | GRCh38.p7 | 9:81655865 | CTCAAAAAAAAAAAA[-/AAAAAG]AAAAGAAAAGAACAA | 7088 |
rs571527868 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678843 | GACTCCATCTCAAAG[-/A]AAAAAAAAAATTAGG | 7088 |
rs571543956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81682303 | AACCCTGGAGGAGGC[A/G]ACCCAACTCAAGCTT | 7088 |
rs571556195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647174 | CCACAAATAGAAACC[C/T]GGCATTTTGTGGACG | 7088 |
rs571583278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652892 | CACCAGTCATTTTCG[G/T]AAACTCCTGGAATTC | 7088 |
rs571601695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591941 | GCAGGCAGTGGGTAC[A/G]TGGCACCATCTGCAA | 7088 |
rs571625125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628675 | AATTATCTCTAGGCA[A/C]GTTCTAAATACAAAC | 7088 |
rs571652753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81681482 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 7088 |
rs571697696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81641641 | GAACAGACATTTCTC[A/G]AAGAAGACACACAAA | 7088 |
rs571776820 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588026 | GCACCTGCGATTGTC[C/T]TTCCCTGTTTTCCAC | 7088 |
rs571814629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597125 | GAATGTGTCTGTTTC[A/G]TGATCCATAAGATAG | 7088 |
rs571829912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81683571 | AGAACTTATTATTAA[C/T]GTGTGACATTCAGAA | 7088 |
rs571836736 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605754 | CAATGGCAACAAAAG[A/C]CAAAATAGACAAATG | 7088 |
rs571841159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602846 | CTGTTAAAAAAAAAA[C/T]GAGTTAAATGGGGAA | 7088 |
rs571854733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587993 | AAACTAACCTTCCCC[C/T]GAGGAGGAGGGGAAA | 7088 |
rs571861049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81679651 | TCAAATAAGCCCACC[A/G]ACAGAAACAGCTGTC | 7088 |
rs571923079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680084 | AATTTGCACGCACGA[C/G]GTGCTGGGTTCTGCG | 7088 |
rs571936262 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81668204 | ATGTAAAGGAAGTTG[A/G]AAGTTGTGGTGGGCA | 7088 |
rs571939821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81609331 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 7088 |
rs571969127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661526 | TAAATTGCAAATTGA[C/T]GGATCATAAAAAAAT | 7088 |
rs571982141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648582 | TGTAAAGAGAACAAT[A/C]ATTATTTAAAATCCC | 7088 |
rs572012402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688029 | GAAGGAGCCCAAAGG[A/G]AGGGAGAAAATTAAG | 7088 |
rs572062134 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666235 | AATCTTTCTCCAAAC[G/T]CCGCAGAGTGAATCA | 7088 |
rs572072687 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81637389 | GAACTGGGTAGTAGA[A/T]TCTGATATCTTACTG | 7088 |
rs572077938 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81600622 | TATTTTTAGCATTTA[A/G]TAGACCAAAAAAAAA | 7088 |
rs572115080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81623962 | TAGGATGTCCAGAGA[C/T]AGAGGTGATTTGCCT | 7088 |
rs572154776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81631830 | CTATCTCACCGGGCA[C/T]GGTGGCTCAGGCCTG | 7088 |
rs572197580 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662742 | GCACCGTAAATTGAT[A/C]TCCAAAATTAAGAGT | 7088 |
rs572221925 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689222 | GCAAAGTTCTCTCAC[C/T]ACCCGAGGGACGACA | 7088 |
rs572235464 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588913 | ACTTTTAACCTGAGC[C/T]TGGATTTTAAAGAGT | 7088 |
rs572238355 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81599919 | TATTTTTTTTAAAGG[C/T]AAATACAAAACTTCT | 7088 |
rs572261909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605813 | ACGGCAAAAAAAAAA[A/C]AACTACCATTAGAGT | 7088 |
rs572285720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684658 | AAACAAGGGTTTGAG[A/G]TGAAATAGCACATAT | 7088 |
rs572289087 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81685148 | CAACAACTGAGAAAT[A/T]TTTCAAAAATTTGTT | 7088 |
rs572320020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81594565 | AAAAAAAATTATGCA[C/G]ATTCTACTTTGAAGA | 7088 |
rs572360027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81681321 | TTGCGAAGCCGAGGC[A/G]GGGGGAATCACTTGA | 7088 |
rs572360424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588894 | CATTCCTGTAGAGCT[C/T]CAAACTTTTAACCTG | 7088 |
rs572365012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81604606 | CTGGGCAGCAGTGGG[A/T]CCCCCATCCTTGGAC | 7088 |
rs572408321 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689825 | CTCCTCGGTCTCCCT[G/T]CCCATCCCGGCCCCT | 7088 |
rs572411757 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81595544 | ACAATTGAGGCTGGG[C/G/T]GCGGTGGCTCACGCC | 7088 |
rs572429256 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686493 | TACAAGTAGACAAAA[A/G]GTCAATAATGAGAAA | 7088 |
rs572449440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638952 | TTTTTGAAGCAAAGT[C/T]TCACTCTGTTACCCA | 7088 |
rs572456793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638255 | ACTATCCCTTGCCCC[C/G]AGCTCTCTTCCAAAG | 7088 |
rs572487023 | in-del | -/TATT | 0.00874735 | 0.0655527 | intron-variant | TLE1 | GRCh38.p7 | 9:81624548 | TATTTGCCAAATAAA[-/TATT]TAATCGAGAATCAGC | 7088 |
rs572491057 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81680702 | CTAAATGCAGAGAGC[G/T]TTCTCTCTTTTAACT | 7088 |
rs572522081 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592553 | CCTGAAGTTAAGGCC[A/G]TAAAACCTAACCAGC | 7088 |
rs572526043 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659376 | ATTTTCCTACCCAAT[C/G]ATGAATACCTATTTG | 7088 |
rs572527149 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614188 | GCTGGGATTACAGGC[C/G]TGAGCCACCGCGCCA | 7088 |
rs572533701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634477 | GAGAGGGAGGAAAGG[G/T]GAAAAAATGCGATTA | 7088 |
rs572544876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687008 | GAGACATCGATTGAA[C/T]CAATGTTTCAGCTCA | 7088 |
rs572582287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644930 | ACCCGGGAAGCGGAG[C/G]TTGCAGTGAGCCGAT | 7088 |
rs572601744 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TLE1 | GRCh38.p7 | 9:81609642 | TGCTTCCCCACGAAG[C/G]CACTTTGCTTTTTAT | 7088 |
rs572632443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617703 | CAAGACTCTGTCACA[A/G]AAAAATAAATAAAAT | 7088 |
rs572658365 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657053 | ATCTAATGGATTAAA[A/T]AATGACCTCATTTTT | 7088 |
rs572660206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81662017 | GTTGGTAAGGCTTCC[C/T]ACAGCTAAGAATTTA | 7088 |
rs572662710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609188 | CACCCAGGTTCAAGC[A/G]ATTCTCTGGTCTCAG | 7088 |
rs572670067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612122 | TTATACACTGGATCC[C/G]TCCTTCCCCAGAGCG | 7088 |
rs572675828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81656092 | GAAATGACTGGTAGA[A/G]AGAGGAAGCCCGTGC | 7088 |
rs572699835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81683747 | AGCTTTTCACGTTTT[C/T]CAAATTGCTAAGCCA | 7088 |
rs572709880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81612648 | TTGGGCCAGCCAAAC[C/T]GCTGTTTCAGCCAGT | 7088 |
rs572716799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81618272 | TGTCAGTGAAGAATA[C/T]AGAAATAATATCTGA | 7088 |
rs572738224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655664 | TGCTTACTAAATGCC[A/T]CCTATATTACTGAAT | 7088 |
rs572740827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647309 | ATCTGCCTTATTCTT[C/T]GTGTTAGGTAAGGAA | 7088 |
rs572770122 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620637 | CTCGATGTGAGAACT[A/T]TTTTTGAAAGGTGAT | 7088 |
rs572779829 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81641891 | GCCAGGTGTGGTGGC[A/G]CATGCCTGCAATCCC | 7088 |
rs572797338 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636475 | GGGAATGCAATGATG[C/T]ATACACAAGCAAGTG | 7088 |
rs572808979 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665747 | GGGCTTGAGTGTGGG[A/G]CCCATCAAAGAATGA | 7088 |
rs572829711 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677636 | CAAGAGGTTGTACGT[A/C]TACCTAGACTAGTAT | 7088 |
rs572847358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646606 | ACTTCACACACTACA[A/G]TCCCATAGATAGCTG | 7088 |
rs572890782 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688326 | GCCGAGGAAAATTAA[A/G]CCGGAAAGCCAAGCA | 7088 |
rs572891412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678074 | TGACTAAGCAGCAAA[C/T]ACTACTATAAGAAAA | 7088 |
rs572910857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615054 | ACCACTGCACTCCAG[C/T]CTGGGTGACAGAGTG | 7088 |
rs572936966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655058 | TTAGTGTCTATAGCA[C/T]GGGCTGTTTTAAAGA | 7088 |
rs573038462 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662474 | GCCGAGGTGGGTGGA[C/T]CACCTGAGGTCAGGA | 7088 |
rs573051548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81659141 | CTCGATCTCCTGATC[C/T]TCGTGATCCGCCCAC | 7088 |
rs573069671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81621530 | ATGTTTGAGCACTAA[A/G]AGGACAGTGTCCAGG | 7088 |
rs573088664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653065 | CTTTGGGAGGCATGA[C/G]AATGTAACATAGAGC | 7088 |
rs573113718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614568 | CTTTCTGACCTTGGA[C/T]CATGAGCCACGGCTG | 7088 |
rs573154480 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688933 | GGCGCGCCGGGAGGC[A/G]GCTCGGCACGCCCCG | 7088 |
rs573165136 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673344 | TTTTAAGCCTAAAGA[C/T]AAATGCTTATGATCT | 7088 |
rs573178719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81669211 | TCATTACTGAATCAT[C/T]TGAGATGATCTGTGG | 7088 |
rs573202069 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81670088 | AAATCATTTGGGTAA[C/T]TGGATATCTTATCTT | 7088 |
rs573204449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628880 | GGAAGCCCTTTCTGA[G/T]AATTTGATGAGTTAT | 7088 |
rs573213983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81658429 | AAATTCTACATAAAT[G/T]GTCTGGAGAAGAAGC | 7088 |
rs573217369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81660256 | CTCAATGAACCAAAA[C/G]TTAATCTCCATGCAC | 7088 |
rs573301428 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605392 | GGTATCTTTTCCCTC[C/T]TATTCATTTGTATTG | 7088 |
rs573317384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81657511 | TGTTACTACCTAGAA[C/T]GGCATCAAAGTAGAC | 7088 |
rs573371207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81665624 | GGGCCTGCATCTCCG[C/G]AGAAAGCTCTCCTAT | 7088 |
rs573465401 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598459 | GTACTTCTCATATGG[C/T]GAACATTTAAGTCTT | 7088 |
rs573498779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587039 | ATGGCAAACACTGTT[G/T]TTTCCAAAACAAGTC | 7088 |
rs573537291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81632077 | CCTGGGTGACAGAGC[A/G]AAGACTCCATCTCAA | 7088 |
rs573561320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81638160 | CCTAATGGCAGTGAC[A/G]GGGGAGTTTACGCTT | 7088 |
rs573571671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651173 | TATAAAGACCAGCAG[C/G]GCATCATCTCACAAG | 7088 |
rs573583857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678975 | CAGAAACCCCATCTC[G/T]ACCAAAAAATAATTT | 7088 |
rs573590375 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643590 | ACCCAGGTGGGATAC[A/G]GTGGCATGATTTTAT | 7088 |
rs573599378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81631713 | TAGATTTAAAACGCA[C/T]AACAGCCTAAAGGGC | 7088 |
rs573635122 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583855 | GAGGTGAACTGCAAG[C/G]AACAGAAAGGTAATC | 7088 |
rs573639921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81613236 | TCTGTTTCTTATCAT[A/G]GCTTTTTCAGAGATA | 7088 |
rs573657104 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605111 | TGGCAACTGTGCCTT[C/G]CGTCTGCCTCACCCA | 7088 |
rs573657843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81625240 | CATCTTCACTGGCAA[C/T]AAGCAAATTGCTATT | 7088 |
rs573658815 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585064 | GGGTCACCACATGAA[A/C]TTCTTCCCTCTTCAT | 7088 |
rs573716148 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669245 | GGATGAGAGGAAAAT[A/C/G]GAAGGCTGTGAGAAC | 7088 |
rs573718370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81585179 | GCTCATAATGACTTC[C/T]ACTGCCCCTGCTCCA | 7088 |
rs573749663 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669822 | TAAATGTTAATAACC[C/T]TGACTTTATACCAAC | 7088 |
rs573759463 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631624 | TGCACTCAATGAACA[C/T]AGCCATTTAAGGTGA | 7088 |
rs573775798 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604328 | GGATCTGGATCTTAG[G/T]GAGCAGGTGATGTGG | 7088 |
rs573791866 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601906 | AACATTTGTTTCCTG[A/G]GTATCTATGCTCAAG | 7088 |
rs573793235 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81624778 | TTTTCATTTAAAATT[A/T]AAAAAATAAACAAAT | 7088 |
rs573803075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81669675 | AAAAACTGCGCATTG[C/T]TGCTAAATAAATCTT | 7088 |
rs573857788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588813 | CAGTAAAGAACTGCG[C/T]GGGAATTTCAACACT | 7088 |
rs573910566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81676648 | CAGGCTATGAGGGAC[A/G]AAGAGGTCATCACAG | 7088 |
rs573910871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682446 | AAGACAAATCACATT[C/G]AAAACTGTTCATTAC | 7088 |
rs573915335 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628039 | GCCTAGGCAACATAC[G/T]GAGACTCTGACTGTA | 7088 |
rs573947257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651594 | AGGCACAAGAAAGAA[C/T]AAGAGCCAACAGTTC | 7088 |
rs574003296 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TLE1 | GRCh38.p7 | 9:81664408 | TCAGGATATCTGCTA[C/T]TCAGAGTCTTAAGAT | 7088 |
rs574004400 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626137 | ATAAAGCACATTATT[C/T]AAATGGATTTCTTTA | 7088 |
rs574024472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81594538 | ACAAGAGCAAGACTA[C/T]GTCTTAAAAAAAAAA | 7088 |
rs574033907 | in-del | -/TT | 0.00438332 | 0.0466095 | intron-variant | TLE1 | GRCh38.p7 | 9:81599865 | TAGGTTGGGAGACTC[-/TT]TGTTTCCTTATTTAG | 7088 |
rs574041872 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655337 | CACTGCACTCCAGCC[C/T]GTGCGACAGTGAGAC | 7088 |
rs574073671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587247 | ATAAATGAACTTTCA[C/G]AGGAGCTGTGACTTT | 7088 |
rs574075588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592795 | CTGTAAACCACTGTA[A/G]AATATTTTTTAAAAA | 7088 |
rs574077764 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81684655 | ATGAAACAAGGGTTT[C/G]AGATGAAATAGCACA | 7088 |
rs574096932 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81596292 | GAACACTCATCCGTC[A/C]CACGGGAAGCCCATA | 7088 |
rs574123967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626849 | CCTCCAGGCAAAACA[A/G]AACAAACTCTGGAGC | 7088 |
rs574134536 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676374 | CTGAGCAAAACAAGT[A/G]CTGTGACAGCCTGCC | 7088 |
rs574149505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81601442 | TAAATTACATGTCTG[A/G]CATTAAAACATAGGG | 7088 |
rs574166253 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682764 | TGAGACATTGTCTAC[C/T]TCTACTGTATAGAGA | 7088 |
rs574179198 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81678795 | CAGTGAGCCGAGATC[A/C/G]AGCCACTGCACTCCA | 7088 |
rs574181222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81684951 | TTGTTCCAGCTCAAT[A/G]CTCTTTTTATACACC | 7088 |
rs574227692 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687111 | GACTCCCTGGAACAG[G/T]GCAAACCGGCAAAAG | 7088 |
rs574242772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81679393 | TTGCAAACAATTTTA[A/G]AAACCATACTTTTGT | 7088 |
rs574287148 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81600880 | GCAAGTGTGCCCTTC[A/G]CTTGAGCTGGAACAT | 7088 |
rs574314933 | snp | A/C/G | 4.46511e-05 | 0.00472482 | missense, synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687405 | CGGGATAGTGAACTT[A/C/G]AAGGGCTGGCCTGCA | 7088 |
rs574524471 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81673374 | TTAGAAGGAAAGAAA[G/T]AAAACACGGTAATGG | 7088 |
rs574539274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81648043 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACCTAAG | 7088 |
rs574548371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81636094 | AATTAGAAGCAAAAT[A/G]GAAAAGGGGATGAGG | 7088 |
rs574549338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81597655 | TTCTGAATCAAGCTC[C/G]TACAGATCAGGATCG | 7088 |
rs574630901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81647618 | GCTACAAGCACTTAG[A/G]GAAACCAGGCAGACA | 7088 |
rs574633187 | in-del | -/C | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690863 | GACGTGGCTAAGGTT[-/C]TTATGAAGTGGAACT | 7088 |
rs574642111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617656 | GCAGTGAGCTGAGAT[C/T]GTGCCACTGCACTCT | 7088 |
rs574654303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81611611 | ACAAGAGGAAGGTGA[A/G]TGTGTGGCTGGGAGA | 7088 |
rs574749030 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686403 | AAGTAGCTACTGCAA[A/T]AAAGTGGGTTGAAGT | 7088 |
rs574769440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649958 | CTTGAAAAGAGCCTT[C/T]GGACATAAATTCATA | 7088 |
rs574777959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81599894 | TAGAGGCATACACTC[C/T]ATTTTCATTTATTTT | 7088 |
rs574807845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81644594 | AATGGTAATGAATAC[A/G]GAGTTTCTTTACAGG | 7088 |
rs574811858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81610793 | TGTCTCCAGATATTA[C/T]CAAATGTCCTCAAGG | 7088 |
rs574816842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81617277 | AGTATTTTTGGAAAG[A/G]TAATAGATGGCAATA | 7088 |
rs574817024 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689785 | GTTCTCCCTCCCCCC[C/G]TCCTCTCGCTTCCAT | 7088 |
rs574836778 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TLE1 | GRCh38.p7 | 9:81680262 | TCAATGAACTACAAC[A/G]GAACCAAGTCAGAGC | 7088 |
rs574871971 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605718 | GCATGGGCAAAGACT[A/T]CATGACTAAAACACC | 7088 |
rs574889687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81593631 | ATGTATCTTGTGTAA[C/T]TGTATGATTTCTTAG | 7088 |
rs574913515 | in-del | -/AAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617149 | AAAAAAAAAAAAAAA[-/AAA]GAATCCTGGAAAGCT | 7088 |
rs574983829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81614340 | CTAAAAAGAACAACA[A/C]TTTGGAGTTAAGAGT | 7088 |
rs575037271 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638134 | GAGACAAATCCACCC[A/T]CACCAACAGGCCTAA | 7088 |
rs575064419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81661402 | ATGAGTGCTGTTTGA[A/G]GCTCAAAACAGGGTG | 7088 |
rs575095276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609445 | CAAAACAGACCTTCA[C/T]ATTTCAATTCTGCTG | 7088 |
rs575100769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81655617 | TGTAAAGAGGCCCAT[C/T]CTTGACCTTACTTAT | 7088 |
rs575140471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81602304 | CCTTGAAGGGCACGT[C/T]GGTTTATACAGGTCG | 7088 |
rs575212872 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673718 | CGGGGAGGGGGCGGC[C/T]TCTGGCGGACCAATT | 7088 |
rs575235698 | snp | A/C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614640 | TGGGATAATGCCTAC[A/C/T]GGGACCAGGTAAGGA | 7088 |
rs575239984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686639 | GGTAAAACTTCATAG[A/G]AACAAGGGAAAGAAA | 7088 |
rs575281658 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671069 | GCTACTTGGGAGGCT[A/G]AGACAGGAGAATAGC | 7088 |
rs575298955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81671826 | CCCCTCCTAAGTTAG[C/T]GGTATGATTTTGGCC | 7088 |
rs575313171 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81596465 | CAGGGGAGGAAATTA[A/T]TCACCTACAATAATA | 7088 |
rs575325189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609111 | CCTTTTTGAGACAGA[G/T]TCTCCTTCTGTCACC | 7088 |
rs575374336 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81665561 | CTTGGGCACAGATAG[A/C]AACACTAATTGCTCC | 7088 |
rs575392276 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81646116 | ACATGTATCCCGGAA[C/G]TTAAATTAAAATTTT | 7088 |
rs575423075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687850 | CCGGGGCCACCTCCA[A/G]ACGCACCGGAACCGG | 7088 |
rs575436301 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642625 | CTTGAACCCAAGAGA[C/T]AGAGGTTGCAGTGAG | 7088 |
rs575480580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634937 | TCTGGGTGGGTGTCT[C/G]ATGCACCACCCAGGC | 7088 |
rs575481206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626236 | GATTGGAAACTCGTG[A/C]CACCTCATTTATCCT | 7088 |
rs575490282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81664213 | TGAGGCCAGGAGTTC[A/G]AGACCAGCCTGGGCA | 7088 |
rs575528583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81658330 | AGTTGGGTTAGACTG[C/G]ATAAGCCTGAAACAG | 7088 |
rs575535575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81634377 | ATGGCGATGGAGGCG[A/G]CATCCAGGGGAAAAC | 7088 |
rs575543685 | in-del | -/ACA | 0.00279162 | 0.0372561 | intron-variant | TLE1 | GRCh38.p7 | 9:81636847 | GTCTCTACTAAAAAT[-/ACA]ACAATAAGCCAGGTG | 7088 |
rs575575665 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688853 | GCAAAGGGGAGCGAG[A/G]TTGAAGACGCAGCGG | 7088 |
rs575600707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586320 | CCGTGCCTGGCCTTG[C/T]TAGGTGACTTTATTG | 7088 |
rs575610260 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81606569 | ACTCATAGGTGGGAG[C/G]TGAACAATGAGAACA | 7088 |
rs575612038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653701 | TCAGTAGCTCTCAAG[C/T]TTATGCTACTTAAAG | 7088 |
rs575613414 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81662164 | TCACAACCATCTACC[A/G]AGTTTTTGAGAAAGT | 7088 |
rs575669120 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81621743 | GCCCTCAAAGCTCCC[C/G]TGAAAACCATGGACC | 7088 |
rs575674126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81622131 | GCAAAGTGCTAACAC[A/G]CCCTCTGAAAAGCTG | 7088 |
rs575726811 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618175 | GGCATATGGAAAAAG[C/G]AGGACATCTCAATGG | 7088 |
rs575754696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81672165 | TTGTTTGAGAGCAGG[C/T]ACTGGCACAACTTGT | 7088 |
rs575763668 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81669113 | GCTGCACTCCTTCTG[C/G]AAGAACAGAAAAGAC | 7088 |
rs575832725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677131 | TAGTCCCAGCTACTC[A/G]TGGGACTGAGGCAGG | 7088 |
rs575851995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81668388 | AAGATTATTTTAAGT[A/G]TTTAGAAGAGAGTAA | 7088 |
rs575922540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81591987 | AGACACCACACCAGG[C/G]CAGGGCAGGGCAGGG | 7088 |
rs575940626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81677551 | GCCTGGGTAACAGAG[C/T]GAGACTCCATCTCAA | 7088 |
rs576008487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81595743 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 7088 |
rs576192907 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586590 | GCATGGCTGTGCTTA[C/T]GGATACAATGATATG | 7088 |
rs576199516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687050 | AATAAATACATGAAG[G/T]GCAAATATTGACGAT | 7088 |
rs576206481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675017 | CAAAAAATAAATTTT[A/T]AAAAAAGTACATGGA | 7088 |
rs576267611 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TLE1 | GRCh38.p7 | 9:81679764 | GGCAACAATAAGCAA[C/T]GGGGAGGGGAGAGGG | 7088 |
rs576280441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81593555 | TTCTGTAAAGCATTC[C/G]CTCAAATCTCATTAT | 7088 |
rs576305635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81680124 | TGGGATGGCTCCCAC[C/G]ATGCGAGGGAACAAA | 7088 |
rs576322964 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690438 | CTCCCACCCCACCCA[C/T]CCCCTTTGCACCCAA | 7088 |
rs576330422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81606591 | ATGAGAACACTTGGA[C/T]ACAGGTGGGGAACAT | 7088 |
rs576333836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589496 | AAGACGCTACCCCAT[A/T]CTATCCAACAGGTAT | 7088 |
rs576341278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686636 | TCAGGTAAAACTTCA[C/T]AGGAACAAGGGAAAG | 7088 |
rs576397725 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589883 | AGGAAAGTAACTGCC[A/G]CACTGTCACCCACAC | 7088 |
rs576402147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81597559 | AGACAGTCAGTCCTG[A/G]ATCCCTCCTTAGGGG | 7088 |
rs576404118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81670898 | GATGGGCTGGGTGCC[A/G]TGGCTCATGCTGTTA | 7088 |
rs576406229 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661549 | AAAAAAATGGTGCTT[A/G]TGCTGAGGGCTGGCA | 7088 |
rs576408741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81625562 | CTTTTAAAATAAAAC[A/T]AAACTAAACATTCCA | 7088 |
rs576410533 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81638265 | GCCCCCAGCTCTCTT[C/T]CAAAGAAGCACGTCA | 7088 |
rs576479924 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81657131 | TTTATTGCTCCACTC[-/TA]TGTTTCCTTTCTCCA | 7088 |
rs576498076 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81659744 | AAACTACTGCTAGGG[C/G]TTCTATGTTAAATCA | 7088 |
rs576505274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81675912 | CACCATGTTGGCCAG[A/G]ATGGTCTCGATCTCC | 7088 |
rs576505376 | in-del | -/AC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680941 | GTTAAAAAAAAAAAA[-/AC]CAAAAAAAACACTAA | 7088 |
rs576571313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81597307 | AAGTGAAGATACGTT[A/G]AATTGAGGGCTTTAT | 7088 |
rs576575102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651153 | TACAAAGTGTCTGAG[A/G]GAACTATAAAGACCA | 7088 |
rs576594583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603144 | CAGCCCCTTCCCCTA[C/T]TGGGTTAGTGCAGCT | 7088 |
rs576597268 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633273 | CTGTGTGGAGAAGTG[C/T]TGTCAGAAGGGGACC | 7088 |
rs576613437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81650048 | ATGGGCCTAAGTCTC[A/G]CTTGCATTGCGCCTG | 7088 |
rs576632076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81603927 | GAATCGCTTGAACCC[A/G]GGAGGTAGAAGTTGC | 7088 |
rs576686508 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655405 | AAAACCTTTGCTCCG[C/T]TCCACATCCACAGCA | 7088 |
rs576749602 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656682 | TTTCTATAATTTGTT[A/G]ATCAAACATGTGTCA | 7088 |
rs576773160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81592240 | GTGGGCGCCCGTAGT[C/T]CCAGCTACTTGGGAG | 7088 |
rs576778451 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680197 | ACTGAAGCCAGGGAA[C/T]GTGTTCATGACTTGC | 7088 |
rs576806413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81619290 | GTTATTAAAGCATAG[C/T]GCAAAGTGTGAACCA | 7088 |
rs576820011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81628926 | TTCTGCAAAAGAGCA[C/T]GGACCCACCCAGTCC | 7088 |
rs576827414 | snp | C/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686789 | CTCTCTCATCCTACC[C/G]AAACCAATCCGAAAT | 7088 |
rs576857787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81649512 | GAATGAGAATGTTTC[A/G]GCTCATTTGCATTTT | 7088 |
rs576859679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81643300 | GGAGTACAATGGTGC[A/G]ATCTCGGCTCACGGC | 7088 |
rs576882815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81635209 | AACGAAACTTTGTTT[A/G]TCCTTTCCTTCCTAC | 7088 |
rs576917667 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81617117 | AACCATTTTCCCATG[G/T]GATTACTAGTTAATG | 7088 |
rs576932534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81673245 | GCCATTGCACTCCAG[C/G]CTGGGGGACAAGAGC | 7088 |
rs576968846 | in-del | -/TGA | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81684733 | CTGTGCAACTTCATC[-/TGA]TGATAATTTTTTAAG | 7088 |
rs577002282 | in-del | -/TTCTGTTAGAAACAATACAAT | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81622506 | AAAAGTAAACTACAC[-/TTCTGTTAGAAACAATACAAT]TTCTGTTAGAAACAA | 7088 |
rs577019523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81642553 | AAAAAAATTAGCCAG[G/T]CATGGTGGTGGGTGC | 7088 |
rs577024031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81653136 | AGGCAGACAAATCTA[C/T]TGTCATATCAGACAG | 7088 |
rs577078331 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617238 | AAGTAAATTAAAAAT[A/G]AACCTTTTTAGCAAT | 7088 |
rs577084060 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588201 | CACACAAAATCCCGA[C/T]TGTATTCCTTATGGG | 7088 |
rs577094051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81615682 | TGCACCACTGCACTC[C/T]AGCCTGGATGATGGA | 7088 |
rs577099256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81609665 | CTTTTTATAATTCTA[C/G]ATCTCTTGGAGCACT | 7088 |
rs577132940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81605083 | GCCTGACAGTTCACA[C/T]TCAGTCTATGAATGG | 7088 |
rs577140484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81622730 | TAGCACCCCTGCTTA[C/T]CTGAAAATGGGCCCC | 7088 |
rs577158567 | snp | A/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689009 | GCCCGACGGGGCTAC[A/T]CCACCGAGAGCAGTC | 7088 |
rs577217379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81651732 | CAGAAGTGAGGAAAG[C/T]ATTTAAAATTCTAAC | 7088 |
rs577255999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81652357 | ATATTCTAACAACAA[A/C]AAGTCAAATGCTGTG | 7088 |
rs577256104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81645629 | CCTATAATCCAAGCT[C/G]CTTGGGAGGCTGAGG | 7088 |
rs577283705 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689737 | TGACGCGCTCCTCCC[C/T]GGAGCGTATGGCAGC | 7088 |
rs577294698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TLE1 | GRCh38.p7 | 9:81611569 | GTTTGGCCCTCACTT[A/G]ATGAAGCAGCATGCT | 7088 |
rs577299679 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81620144 | GGAGGCGGGGGGCCC[A/G]GGGGACTCCTAACAA | 7088 |
rs577314442 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666451 | CATCATCATCACTGG[C/T]TGAAGGTTAAAATTA | 7088 |
rs577389137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81654674 | ATGGCACACCATGAC[A/C]CATTTATGTCATTAT | 7088 |
rs577394057 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597075 | TCTCTGGCTACGTCA[A/G]CTGCGGTCTTGCCAA | 7088 |
rs577418402 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617684 | TCTGGCCTAGCCGAC[A/G]TAGCAAGACTCTGTC | 7088 |
rs577426902 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689298 | GGCCACCCTCCCCGG[C/T]GGGCAAACTCTGCGG | 7088 |
rs577450910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81629811 | GGTACAGTAAAAATA[C/T]GGTGTTATACACTTA | 7088 |
rs577461097 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616389 | TTGCCTAGAGGGCAC[C/T]GGAAGGAAAGGGGAG | 7088 |
rs577468689 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677754 | CAAGATTTGGACGCG[-/C]CAAGTTCAAACACAC | 7088 |
rs577470517 | snp | A/G/T | 0.00130492 | 0.0255103 | missense, synonymous-codon | TLE1 | GRCh38.p7 | 9:81590812 | TTGCTCACCTCACTA[A/G/T]TGTCTGGTTGTGCAG | 7088 |
rs577506221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81667419 | AAGAAGCAAAAATCA[A/G]GTTACCTCTGAATGT | 7088 |
rs577513954 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587150 | TCTAGTCAGCCACCA[A/G]TTCATTTTTTAAAGG | 7088 |
rs577536356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81625338 | TGACAGCAAAAGAGC[C/T]GGTCAGAAGAAAAGA | 7088 |
rs577576969 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | TLE1 | GRCh38.p7 | 9:81599432 | CAACATAAGGCATGT[C/G/T]GACATCGTGAGTGTG | 7088 |
rs577594891 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653481 | CTAAACAAAATAGCT[G/T]ATACATACATATGAC | 7088 |
rs577597777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664926 | CTTGGACTGGGGAAC[A/C]TGCTTTGAGAAGCAC | 7088 |
rs577642178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81666706 | CTTGAACCCGGGAAG[A/C]GGAGGTTGCAATGAG | 7088 |
rs577666953 | snp | A/C/T | 0.0091479 | 0.0670627 | intron-variant | TLE1 | GRCh38.p7 | 9:81677489 | AAAATGGTGTGAACC[A/C/T]GGGAGGCGGAGCTTG | 7088 |
rs577678613 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687503 | AAGCAGTAAGTCAGA[A/G]AAGGCAAGAACGGGT | 7088 |
rs577681866 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650485 | ATTCATTTGGGTGAA[A/G]AAATTCTGTGCTTGA | 7088 |
rs577698820 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TLE1 | GRCh38.p7 | 9:81649343 | ACAACCTCTCTCTGT[-/C]TCCTCGAAGAGCACC | 7088 |
rs577732024 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649081 | GTAGTTATTATTCTG[C/G]CAGTCATCAAATTTG | 7088 |
rs577760293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81664516 | GCTTTTGTTTAAAAT[A/G]TAATTATGCCGATAA | 7088 |
rs577789862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81663515 | CACAAGGACAAGTCC[A/G]CATGATCCCTCAGCC | 7088 |
rs577861833 | snp | C/T | 1.66585e-05 | 0.00288599 | intron-variant | TLE1 | GRCh38.p7 | 9:81613344 | TGGGAATGGGAGAAA[C/T]CAAACAAAGCACAAC | 7088 |
rs577890051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81646134 | AAATTAAAATTTTTT[A/T]AAAAAAGGAAAGAAA | 7088 |
rs577898600 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583935 | GGCTGTCATGTGAGT[C/T]GGCAGATTCCGTTCC | 7088 |
rs577936142 | in-del | -/TC | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81683651 | TGCACAGCACTCTAG[-/TC]TTAAGGGTCTGTCAG | 7088 |
rs577939037 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601533 | CTGACCTCTAGGTGC[C/T]AATATATAAGGCAGG | 7088 |
rs577945981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81585750 | AATAGCAAGAATGGG[G/T]GGAAGTAATCAGCCA | 7088 |
rs577964848 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81677563 | GAGCGAGACTCCATC[-/T]CAAAAAAAAAAAAAA | 7088 |
rs577975480 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668769 | TTTAAAATTATAAAG[C/T]CTTACAGTATTGTCT | 7088 |
rs578019934 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TLE1 | GRCh38.p7 | 9:81676062 | ACTTGTTGAAGGATC[C/T]TGAGATGCACACAAA | 7088 |
rs578022065 | snp | A/G | 0.000254001 | 0.0112666 | intron-variant | TLE1 | GRCh38.p7 | 9:81634320 | TTGGTGGTGGTGGTG[A/G]GAGAGAAAAAGGAGG | 7088 |
rs578131947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81590683 | TCCCTCATCACCTAG[A/C]CCCATGCCTGGCATT | 7088 |
rs578132402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81626906 | TAATTTTTAAATAAC[C/G]TCATGACACTGCCGT | 7088 |
rs578156094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81633686 | GAATTAAAGCCTATG[A/C]AACTAAGTAGTAACA | 7088 |
rs578158130 | snp | C/T | 4.51967e-05 | 0.00475356 | intron-variant | TLE1 | GRCh38.p7 | 9:81620906 | GGTCAGGAATACGAA[C/T]GGCCTATGAGCAAAT | 7088 |
rs578172487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81682111 | AAAAAAAAGTTAGCC[A/G]GGCATGGTGGCGGAC | 7088 |
rs578202613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81640397 | ACAATTTCAAAAATT[A/T]AAAAAAAAAAAAAAT | 7088 |
rs578249057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TLE1 | GRCh38.p7 | 9:81601528 | TATTACTGACCTCTA[A/G]GTGCTAATATATAAG | 7088 |
rs745336329 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630161 | AACAGTAAGGAGTTC[A/G]TCTTATTTATGGCCA | 7088 |
rs745364753 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656345 | TTGGTAGGTATCCTA[C/T]TTAGGTCCTTGCTCC | 7088 |
rs745410818 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681584 | AAAATTCTTCACCAT[C/G]CTGGAGAGCCCAGTG | 7088 |
rs745424799 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621386 | TGTTACAATGAGTTC[-/T]TTTAAGTGTGGGATT | 7088 |
rs745425249 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668656 | TATGGGACAGAATCT[A/G]TTCAGAGTTACAGGG | 7088 |
rs745436692 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618538 | TTCAAATTACAACCA[A/G]TGAGGAAGCCTGGGT | 7088 |
rs745458088 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640322 | TCCTTTCATCGCCAT[C/T]TGAGTACCCTGTCAC | 7088 |
rs745458373 | snp | C/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585810 | AAGTGATCTAACGCA[C/G]ATGAACCAAGTGTCA | 7088 |
rs745475611 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680288 | AGAGCCTATAGTTCA[C/T]GGCCACTCCCCACAG | 7088 |
rs745483064 | snp | A/C | 0.000124945 | 0.00790298 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687310 | ACGCCCGCGACCACT[A/C]GCATGGCGCGGCCGG | 7088 |
rs745485420 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678507 | CATGCCTGGCTTGCA[A/C]CTTAGTAATTATTAA | 7088 |
rs745498247 | snp | A/G | 2.28553e-05 | 0.0033804 | intron-variant | TLE1 | GRCh38.p7 | 9:81620912 | GAATACGAATGGCCT[A/G]TGAGCAAATCTTGAG | 7088 |
rs745529093 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599014 | ATGTGGGCACCAAGC[C/T]TAACTAACTTGAGCC | 7088 |
rs745537158 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626157 | GGATTTCTTTAGCTG[-/C]CATGCTGATTCCCCT | 7088 |
rs745572197 | snp | C/T | 1.65146e-05 | 0.0028735 | missense | TLE1 | GRCh38.p7 | 9:81585601 | CCTCCACATTGCTGC[C/T]CTCCATGCCCACTGC | 7088 |
rs745581190 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639702 | ATTCTTTGTGCCTCA[G/T]CCTCCACAGTAGCTG | 7088 |
rs745632436 | snp | G/T | 1.65141e-05 | 0.00287346 | intron-variant | TLE1 | GRCh38.p7 | 9:81653957 | TTGCACTTTAACAGC[G/T]GAACAATTTTACTTA | 7088 |
rs745637799 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647858 | GTGGATTACCAAAAA[C/T]ACCATGAAATGGACC | 7088 |
rs745651506 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636668 | GAGGTGGGATTCTTA[G/T]GTCAGACCAAACATA | 7088 |
rs745683544 | in-del | -/T | | | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689659 | CCGGGAGGTTGGGGG[-/T]GTGGGGGGGGGGCAG | 7088 |
rs745687051 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646709 | GGAGAGCCCTTTAGG[G/T]CTACAACTCAATCTC | 7088 |
rs745687169 | snp | A/T | 1.64779e-05 | 0.00287031 | missense | TLE1 | GRCh38.p7 | 9:81593065 | CTCTTATTGCCAGGG[A/T]GGCTGATGTCCCAGA | 7088 |
rs745712794 | in-del | -/TTA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683561 | ATGCCTCCTCAGAAC[-/TTA]TTATTAATGTGTGAC | 7088 |
rs745722282 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81652253 | CATGGTCACCTGTTT[A/G]GCACGTTCAACAGCC | 7088 |
rs745742177 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657253 | TGCCACTTGTCTTTC[A/G]ACCTTGCTTAATATG | 7088 |
rs745775897 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604743 | TGAACTCTTCTGGCT[A/G]TAACACTCAGGAGGC | 7088 |
rs745798467 | in-del | -/AT | 1.66441e-05 | 0.00288474 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685759 | GCATTTCATTAACTC[-/AT]GTTTTTTACACTCTG | 7088 |
rs745837464 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675770 | CAGTGGCATGATCTC[A/G]GCTCACCACAACCTC | 7088 |
rs745867735 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602480 | AGACCTTATGCACTT[A/C]GCCTGAAGGTGATTT | 7088 |
rs745931954 | snp | C/T | 1.6941e-05 | 0.00291036 | intron-variant | TLE1 | GRCh38.p7 | 9:81613572 | TTAATCCAAGCCATA[C/T]TACACAATTTATCAC | 7088 |
rs745967038 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643135 | CCCAAGATAAAGAAG[A/G]TCTGGATTTCCAAGG | 7088 |
rs745995521 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684211 | AATTCACTTAAATGA[C/T]GATAGATGTTAGCCA | 7088 |
rs745996779 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592559 | GTTAAGGCCATAAAA[A/C]CTAACCAGCTCTCTC | 7088 |
rs746010630 | snp | A/C | 3.81228e-05 | 0.00436577 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688168 | ACCGCCCGGGAGAAG[A/C]GCCTCCCCAACGATC | 7088 |
rs746135069 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627404 | TCCAGTCCCACCAAG[G/T]CCCCGATATCCACCT | 7088 |
rs746145813 | in-del | -/TGTGTGTGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662378 | GTGTGTGTGTGTGTG[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 7088 |
rs746177488 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585090 | TTCATCCTCACTGTA[A/G]AGTAGAGTGTAACTA | 7088 |
rs746188354 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650822 | ATTTAAGCTGAAAAT[C/T]CACTGAAGCTCCCCA | 7088 |
rs746192701 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81608994 | AAAAAAAGCAACAAC[A/G]TTTGCAAAGATCTGC | 7088 |
rs746197081 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622869 | GAAACACCACACTCA[A/G]ACCCAGGGATCCCTG | 7088 |
rs746198272 | in-del | -/GTTCCT | 1.67128e-05 | 0.00289069 | intron-variant | TLE1 | GRCh38.p7 | 9:81593009 | TGCCCTTGTGCACCA[-/GTTCCT]GTTCACTCACCAGAC | 7088 |
rs746204682 | snp | C/T | 0.000264314 | 0.0114929 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585518 | ACCACAGTAAGCAAA[C/T]TTCAGGGACAGCACG | 7088 |
rs746219710 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683771 | TAAGCCAATTATACA[C/T]AGCATATTATTAATG | 7088 |
rs746222964 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660526 | TCATGCCATTCTCCT[A/G]CCTCAGCCTCCTGAG | 7088 |
rs746230106 | snp | C/T | 6.06299e-05 | 0.00550557 | intron-variant | TLE1 | GRCh38.p7 | 9:81600139 | GGACAAAGATACAAA[C/T]GGAGAAATTCTTGGA | 7088 |
rs746233162 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634631 | TATTAAGCAAGGCTG[C/G]CTACATCAGTAAGTA | 7088 |
rs746241400 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660211 | AAACTGATGCCAGGG[C/T]ACATATTTAATATAC | 7088 |
rs746241827 | snp | A/G | 1.68015e-05 | 0.00289836 | intron-variant | TLE1 | GRCh38.p7 | 9:81616145 | GGGTCCTCAACAAGC[A/G]TAATCAAAAGTTTTC | 7088 |
rs746282181 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603612 | AAGTTTTCCCCCAAT[A/G]TATCTATCTCTTAGT | 7088 |
rs746290039 | snp | C/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690135 | CCCTTTAATGAAAAT[C/T]CTCAGATCTAAGTGA | 7088 |
rs746329867 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616066 | AGCATCCTTCTTTAG[C/T]AGGCGATTTTTGTCG | 7088 |
rs746342572 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627112 | ACTTGACTAAGTCAT[C/T]TGTGTATCGGACAGC | 7088 |
rs746371911 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594465 | CATGTTCTCACTCAT[A/G]AATGGGAGTTGGACA | 7088 |
rs746394112 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592932 | GGGCTTCTATTTCCT[C/G]ATAATGGGAATAAAA | 7088 |
rs746406716 | in-del | -/A | 1.66142e-05 | 0.00288216 | intron-variant | TLE1 | GRCh38.p7 | 9:81613357 | AACCAAACAAAGCAC[-/A]ACAAGAGGCGATGCT | 7088 |
rs746408142 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649947 | ATCACCACAAACTTG[-/AA]AAGAGCCTTCGGACA | 7088 |
rs746432462 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585746 | GGGAAATAGCAAGAA[C/T]GGGGGGAAGTAATCA | 7088 |
rs746435532 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609858 | AGCTGACTGCCCACA[C/G]CACAGCACTGTTGGG | 7088 |
rs746459966 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597986 | GTTGTTGGTTTCCTG[C/G]AAATAGGAACTGCAG | 7088 |
rs746482800 | snp | A/G | 1.64874e-05 | 0.00287113 | missense, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81652275 | TCAACAGCCTGGGCC[A/G]CCTGTTGTTGATGCT | 7088 |
rs746485098 | in-del | -/A | 1.65247e-05 | 0.00287438 | intron-variant | TLE1 | GRCh38.p7 | 9:81653951 | ACATAATTGCACTTT[-/A]ACAGCTGAACAATTT | 7088 |
rs746494596 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626923 | CATGACACTGCCGTT[-/C]CCCAGCTCAGGACCT | 7088 |
rs746513420 | snp | C/T | 4.94262e-05 | 0.00497098 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81613456 | GGCGCTGGTGCCCGG[C/T]GTTGGCATGTCGCTC | 7088 |
rs746552529 | in-del | -/GTT | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691305 | CATTTCACTGTTGGA[-/GTT]GTTTTTAAATATGTA | 7088 |
rs746553493 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650496 | TGAAAAAATTCTGTG[C/G]TTGAGCTACAAGTAC | 7088 |
rs746553545 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638650 | TCTTTTTTTGAGACA[C/G]AGTCTTCACTGTTGC | 7088 |
rs746574968 | in-del | -/GCAGCAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633325 | TGTGTGTGTGTGTGT[-/GCAGCAG]GCGTTTGAGTACTTA | 7088 |
rs746612671 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660146 | GCATTACGAGAACAC[A/G]ACTCCTACTAAATAC | 7088 |
rs746617245 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658489 | CAAGACTTCCCCTCC[A/G]TCTGCCAGGTCTCTA | 7088 |
rs746623029 | snp | C/T | 0.000188893 | 0.00971652 | intron-variant | TLE1 | GRCh38.p7 | 9:81634022 | GGTTGGGGCTCTCTT[C/T]AGCGATGCACACAAC | 7088 |
rs746624480 | snp | C/G | 1.6577e-05 | 0.00287893 | intron-variant | TLE1 | GRCh38.p7 | 9:81613362 | AACAAAGCACAACAA[C/G]AGGCGATGCTGTACC | 7088 |
rs746655615 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81608727 | AGATCAGCTGAGGTC[A/G]GGAGTTCAAAACCAG | 7088 |
rs746702216 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594161 | TGCCCTCTTCTCTTC[C/T]TCCTTCCCACTGCCT | 7088 |
rs746703833 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622015 | GGATGAAAGGTGAGC[C/T]GGCTGGATCCCCGAA | 7088 |
rs746720642 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682869 | TCTTAGTGCTACCAT[C/G]AAAGACTTAAGTATC | 7088 |
rs746763201 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603981 | CACTCCAGCCTGGAT[A/G]ACAGAACGAGACTTT | 7088 |
rs746776983 | snp | C/G | 1.64849e-05 | 0.00287092 | missense | TLE1 | GRCh38.p7 | 9:81620534 | TGTGCCTCTTAGACT[C/G]TCTGGGACCAGGAGG | 7088 |
rs746783887 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617645 | AGGTGCAGGTTGCAG[C/T]GAGCTGAGATCGTGC | 7088 |
rs746797205 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616528 | TAACTTCTTAATGTA[A/G]GAAGTTGCAAGAGGT | 7088 |
rs746800915 | snp | A/G | 3.30169e-05 | 0.00406293 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685791 | CTAACACGTTTGCTA[A/G]TATCATATGAAAAAG | 7088 |
rs746803137 | snp | C/T | 2.40845e-05 | 0.00347011 | missense | TLE1 | GRCh38.p7 | 9:81611783 | CCATGGGGGAGCGCC[C/T]GTAGGCCACCACGGC | 7088 |
rs746835023 | snp | C/G | 3.30508e-05 | 0.00406501 | missense | TLE1 | GRCh38.p7 | 9:81620455 | CATAGTGGCTGGAGT[C/G]CTTATCATCCACCTT | 7088 |
rs746852099 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684880 | ACTACTCAATCGAGG[G/T]TCCTTTGGGCTGAGC | 7088 |
rs746888017 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668399 | AAGTATTTAGAAGAG[A/C]GTAAGCAAAAGGATC | 7088 |
rs746892794 | in-del | -/AAAAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645750 | TGTCTCCAAAAAAAT[-/AAAAT]AAAATAAAATAAAAT | 7088 |
rs746909078 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641998 | TTGCACTCCAGCCTG[A/G]GCAACAAGAGCAAAA | 7088 |
rs746917533 | snp | A/C | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81590038 | CAAACAAGCCACAGA[A/C]CCCAAACTGCACCAT | 7088 |
rs746921914 | in-del | -/AAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595815 | CAGAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 7088 |
rs746929161 | snp | A/T | 1.64991e-05 | 0.00287215 | synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81654001 | AAATGGGATGACTTG[A/T]GCACAAATCGTATTC | 7088 |
rs746930620 | in-del | -/TGTGTGTGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662362 | TTAGTGTGCCTGTTT[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 7088 |
rs746938523 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598680 | CTTTTCCCAGGCAAC[A/G]TCTAGCAATTATACC | 7088 |
rs746970030 | snp | A/G | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589528 | TACTCCCCAGGAGCC[A/G]GCACGGAGCAAGGGT | 7088 |
rs746983470 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628951 | CAGTCCATCCATGAA[C/T]GCCACTGCGTAGGTC | 7088 |
rs746993989 | snp | A/C | 1.64906e-05 | 0.00287142 | intron-variant | TLE1 | GRCh38.p7 | 9:81584327 | GAGAAAACAATGGAC[A/C]TGTGTTTAATGTGGA | 7088 |
rs747013039 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640304 | ATTCAATCACATTCA[C/G]TGTCCTTTCATCGCC | 7088 |
rs747017689 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | TLE1 | GRCh38.p7 | 9:81593204 | GGGGGATTCCGGGTC[C/T]GATGAGGGCGTCGGG | 7088 |
rs747044616 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666573 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACTA | 7088 |
rs747053248 | snp | C/G | 1.69112e-05 | 0.0029078 | intron-variant | TLE1 | GRCh38.p7 | 9:81616155 | CAAGCATAATCAAAA[C/G]TTTTCGTGATTTAGC | 7088 |
rs747077317 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626035 | CTCTGCCAACAAGTT[C/T]GAACCCTGAAACCAC | 7088 |
rs747079630 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653522 | AATGTATTTTGGACT[A/G]TTATCATCCACCCCT | 7088 |
rs747080871 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654350 | ATACACATATATATA[C/T]GTATTTTTGAGACAG | 7088 |
rs747100379 | snp | C/T | 3.29554e-05 | 0.00405914 | missense | TLE1 | GRCh38.p7 | 9:81616080 | GCAGGCGATTTTTGT[C/T]GATTCCATTTTCCCG | 7088 |
rs747123587 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665550 | GCTGAAGGCTGCTTG[A/G]GCACAGATAGCAACA | 7088 |
rs747168754 | snp | A/C/T | 0.0103455 | 0.0711759 | intron-variant | TLE1 | GRCh38.p7 | 9:81652145 | CACACACACGTAAAG[A/C/T]CATCAAATTAATAAG | 7088 |
rs747185316 | snp | C/T | 2.53444e-05 | 0.00355971 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688287 | GGCAACTCAATTCTC[C/T]GGTCAATTTCCAACT | 7088 |
rs747192255 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634762 | GGGATTAAAATGGGG[G/T]TGGGGATGCATCCCA | 7088 |
rs747212460 | in-del | -/CGTGTGTGTGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633288 | TTGTCAGAAGGGGAC[-/CGTGTGTGTGTG]TGTGTGTGTGTGTGT | 7088 |
rs747251947 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596339 | AGTCACAGGGGGCCT[C/T]GCAGGAAGCTGGTGC | 7088 |
rs747265334 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637295 | CTTGGAAAGCAGAGG[C/T]TGTAGTGAGCTGAGA | 7088 |
rs747279568 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592705 | GCAGGGATCAGAGTC[C/T]AGGCCCAGTTGTGCT | 7088 |
rs747331545 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633154 | AAAAAGACAAGAGCA[C/G]AGCGAACAGTCATAT | 7088 |
rs747337130 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643907 | ACCACTGCCTTGCTC[A/G]TCCCATTTCCCTGGA | 7088 |
rs747342975 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681068 | CTAAAGAACAACGCA[C/T]TTTTCTAAGAGAAAT | 7088 |
rs747344303 | snp | C/G/T | 0.00132102 | 0.0256677 | intron-variant | TLE1 | GRCh38.p7 | 9:81633336 | GTGTGCAGCAGGCGT[C/G/T]TGAGTACTTACTGTG | 7088 |
rs747416621 | in-del | -/TCCTTAGACGACCA | 3.40385e-05 | 0.0041253 | intron-variant | TLE1 | GRCh38.p7 | 9:81590780 | AAAGAAGCGAACCCC[-/TCCTTAGACGACCA]TCTTTGCTCACCTCA | 7088 |
rs747453961 | snp | C/T | 1.67475e-05 | 0.00289369 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685923 | AAACAGGCAACTTAA[C/T]GTAAACATTATGTCA | 7088 |
rs747468498 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant | TLE1 | GRCh38.p7 | 9:81610169 | AGTCTGCTAATACCA[A/G]TGACTGAGTAACCAC | 7088 |
rs747474384 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684110 | CTTACTCTTCCATAA[C/T]ATCTGTTATCCAAAA | 7088 |
rs747506406 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602324 | TATACAGGTCGAACA[A/T]CCCTTATCCAAAATG | 7088 |
rs747561328 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601680 | CAGGGGAATAAATGT[A/C]CTAAAACTAAAAATG | 7088 |
rs747561388 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614433 | AGCAAGGGGCCTTTC[A/G]GAGACCAGACAGTAA | 7088 |
rs747568083 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621953 | GGAGGGACCAACGCA[A/G]TTCAATATAGAGAAG | 7088 |
rs747588297 | snp | C/T | 1.65026e-05 | 0.00287246 | missense | TLE1 | GRCh38.p7 | 9:81620463 | CTGGAGTCCTTATCA[C/T]CCACCTTCCTTTTCT | 7088 |
rs747602772 | snp | A/G | 4.94523e-05 | 0.00497229 | missense | TLE1 | GRCh38.p7 | 9:81584492 | GCCAAGCATTGAGGA[A/G]GTTATCTTTTCCAGT | 7088 |
rs747665429 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | TLE1 | GRCh38.p7 | 9:81593207 | GGATTCCGGGTCCGA[C/T]GAGGGCGTCGGGGGG | 7088 |
rs747705120 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687894 | TGTAAATAGGCGAGA[A/G]GAGAAACAAAGGGGG | 7088 |
rs747744772 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658441 | AATGGTCTGGAGAAG[A/C]AGCAAATAGGAGCAA | 7088 |
rs747747002 | snp | A/C/T | 0.000168618 | 0.00918071 | intron-variant | TLE1 | GRCh38.p7 | 9:81613561 | GAGTATTATTTTTAA[A/C/T]CCAAGCCATATTACA | 7088 |
rs747776851 | in-del | -/ACACACACAA | 2.7442e-05 | 0.00370408 | intron-variant | TLE1 | GRCh38.p7 | 9:81652140 | CACACACACACACGT[-/ACACACACAA]AAAGCCATCAAATTA | 7088 |
rs747783944 | in-del | -/TGTGTGTGT | 0.000117 | 0.00764764 | intron-variant | TLE1 | GRCh38.p7 | 9:81633312 | GTGTGTGTGTGTGTG[-/TGTGTGTGT]GTGTGCAGCAGGCGT | 7088 |
rs747820945 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81619676 | ATCCATCCTGAAACA[A/G]ACACTCAGGGACACA | 7088 |
rs747847198 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678764 | TAATCCCGGCTACTC[A/C]GGGAGGTAGAGGTTG | 7088 |
rs747886690 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679678 | GTCTAAAATTTACTT[-/A]AAAAACCACTATACT | 7088 |
rs747888432 | snp | C/T | 6.86189e-05 | 0.00585702 | missense | TLE1 | GRCh38.p7 | 9:81611891 | CGCCGTTCATGCCAG[C/T]GTGGGGGACCATCCC | 7088 |
rs747903397 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614727 | TTTGATTGAATGAGT[A/G]ACCACATGAGTGGGT | 7088 |
rs747921535 | in-del | -/CTAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647226 | ATCTGACGATGTCTT[-/CTAA]CTCTCTCTTCCCTCC | 7088 |
rs747947023 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655400 | CTGGAAAAACCTTTG[C/T]TCCGCTCCACATCCA | 7088 |
rs747978062 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639383 | ATCTGTACTCTCTAA[A/C]CAAAACCTGCCCGTC | 7088 |
rs747979958 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671478 | GGTGAAACCCCACCT[C/T]TACTAAAAATACAAA | 7088 |
rs748004182 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666893 | GAGAGCAAGGTAAGA[A/G]GATCACCGCAGAGCA | 7088 |
rs748076579 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597858 | GCAGCTGTGGTGAAC[C/T]GGAAAACAAGACTGT | 7088 |
rs748079107 | in-del | -/AAC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618030 | ACTCCGTCTCAAAAC[-/AAC]AACAACAACAACAAA | 7088 |
rs748119844 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585961 | ACACTAACTGAAATA[C/T]GATCATATATCACCT | 7088 |
rs748135676 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81608552 | TGACATGCAAGTGAC[A/G]TACTGATAAAAGCTG | 7088 |
rs748174556 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624364 | AAAGGCCTCAGCAGA[A/G]TGACAAAGCAGCCCA | 7088 |
rs748179762 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596295 | CACTCATCCGTCCCA[C/T]GGGAAGCCCATATGG | 7088 |
rs748185280 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663115 | CCCCCCAAAGTGCTG[A/G]GATTACAGGCACAAG | 7088 |
rs748187374 | snp | C/T | 5.91116e-05 | 0.0054362 | intron-variant | TLE1 | GRCh38.p7 | 9:81610185 | TGACTGAGTAACCAC[C/T]TTTAAAACAAAACCA | 7088 |
rs748230860 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652621 | ATCACCCTTGTTCAC[A/C]AAAGGGGTTCATAAG | 7088 |
rs748251665 | snp | A/T | 0.000124634 | 0.00789312 | intron-variant | TLE1 | GRCh38.p7 | 9:81610301 | TCAAACCCCACCTGG[A/T]AACAAAAATAAGGCA | 7088 |
rs748270335 | snp | A/C | 1.64817e-05 | 0.00287064 | intron-variant | TLE1 | GRCh38.p7 | 9:81616707 | TCACTGTCCTGGAAA[A/C]AAGAAACATTAACGC | 7088 |
rs748275109 | snp | A/G | 1.70435e-05 | 0.00291915 | intron-variant | TLE1 | GRCh38.p7 | 9:81616164 | TCAAAAGTTTTCGTG[A/G]TTTAGCTTGTAACAG | 7088 |
rs748285080 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606135 | AACAGATGCTGGAGA[C/G]GATGTGGAGAAATAA | 7088 |
rs748321881 | snp | G/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686611 | CAATACAGTTATTTC[G/T]GAGTTAGAATCAGGT | 7088 |
rs748328111 | snp | G/T | 1.6476e-05 | 0.00287014 | missense, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81652242 | TTCAATTCTGCCATG[G/T]TCACCTGTTTGGCAC | 7088 |
rs748375627 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646638 | CAGCTATAGCCAAAG[A/G]AGAAAAATAATCCAA | 7088 |
rs748397703 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601305 | ATCACTGCTGCAAGT[A/G]TTTTCCTATGAGGCA | 7088 |
rs748427807 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81635065 | AAATTGCTGAAACTC[C/T]ATCCCTAGGCAAGAG | 7088 |
rs748436775 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631644 | ATTTAAGGTGAAACA[C/G]GAGTACTGAAGAAAA | 7088 |
rs748442956 | in-del | -/GTGTGTGTGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662385 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTG]TGTGTGTGTGTTTAA | 7088 |
rs748479205 | snp | C/T | 3.29516e-05 | 0.00405891 | missense | TLE1 | GRCh38.p7 | 9:81613467 | CCGGCGTTGGCATGT[C/T]GCTCCGAGGCGTTGG | 7088 |
rs748494465 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644759 | AGCACTTTGGGAGGC[A/C]GAGACAGGTGAATCA | 7088 |
rs748518689 | snp | A/G | 7.37055e-05 | 0.0060702 | intron-variant | TLE1 | GRCh38.p7 | 9:81634052 | CTTTGCAGCACTGTA[A/G]GAGTATGAGGACAAA | 7088 |
rs748551593 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641700 | AATATCATTAATCAT[G/T]AAGGAAACGCAAATC | 7088 |
rs748581546 | in-del | -/ACAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627270 | TTCTAATTACAGAGC[-/ACAA]ACTCAAGTCAAAAAG | 7088 |
rs748589393 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607813 | ACTGGAAGAGAACTA[C/T]CAGCTAAGTGAACAT | 7088 |
rs748644654 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612827 | CTTTGGGAGGCCGAG[A/C]TGGGCAGATCACCTG | 7088 |
rs748678855 | snp | C/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687838 | TTCCCAGAGTCGCCG[C/G]GGCCACCTCCAGACG | 7088 |
rs748689804 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625302 | AACTTGCACTAATAG[A/G]ATGACAGAACAGAAT | 7088 |
rs748709411 | snp | A/G/T | 9.99894e-05 | 0.00707011 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687330 | GGCGCGGCCGGACAC[A/G/T]CACCTGTGATACTGC | 7088 |
rs748719066 | snp | A/T | 1.71211e-05 | 0.00292579 | intron-variant | TLE1 | GRCh38.p7 | 9:81585699 | TATTCCGCCTGATAC[A/T]CTTAGGAAGGGAAGA | 7088 |
rs748719984 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586823 | ATTGTATCCTGCTTA[C/T]GTTGGGAAAGAGTGA | 7088 |
rs748732283 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611651 | TTTGTCTCCGAGGTG[C/T]GTGGGGCTGGCTGCT | 7088 |
rs748737695 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675384 | CTGGTGACAAGTCAA[C/G]TTTAATGCCTTGAGA | 7088 |
rs748806534 | snp | C/T | 1.64944e-05 | 0.00287175 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685830 | CCAATCTTTGATACC[C/T]ACCATCACATAGTGC | 7088 |
rs748815986 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675869 | CCACGCCCAGCTAAT[A/T]TTCGTATTTTCAGCA | 7088 |
rs748826490 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670848 | GGACCCTTTCGGTAG[A/G]TAAGCCATACTTAAT | 7088 |
rs748846358 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631525 | TCACTCACTCCTCCT[C/T]GATTCTCTGGGAAAG | 7088 |
rs748854544 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657299 | AGAACTTTAAGTCTT[A/T]ATGTGGTCAAATGAA | 7088 |
rs748860571 | snp | A/G | 4.94907e-05 | 0.00497422 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81620546 | ACTGTCTGGGACCAG[A/G]AGGGAATTACTCTGC | 7088 |
rs748878748 | in-del | -/CA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617133 | GATTACTAGTTAATG[-/CA]AAAAAAAAAAAAAAA | 7088 |
rs748881805 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682619 | AAACCATATGACAGA[C/T]AAAAACATTTAAAGA | 7088 |
rs748903709 | snp | C/T | 1.67066e-05 | 0.00289016 | missense, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81685719 | TATGACATTTCATAA[C/T]ACTGTAAAGAGAAAA | 7088 |
rs748911791 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669635 | CACACCAAAAGACAT[A/G]CACACAAAGAGGAAG | 7088 |
rs748962150 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630256 | GGCAGATTCTCTTCC[C/T]AAACGTCAACTAAAT | 7088 |
rs748984572 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682252 | GCGAGATTCCATCTC[-/A]AAAAAAAAAAAAAAA | 7088 |
rs748985884 | snp | A/G | 0.000127113 | 0.00797123 | intron-variant | TLE1 | GRCh38.p7 | 9:81600050 | GATTCTGAGTTCTAG[A/G]ACCTAACTTCCTCTA | 7088 |
rs748986061 | snp | C/T | 1.64912e-05 | 0.00287147 | missense | TLE1 | GRCh38.p7 | 9:81584513 | CTTTTCCAGTACTCA[C/T]AAACCATTTACCTAG | 7088 |
rs749019160 | snp | C/T | 3.44632e-05 | 0.00415095 | intron-variant | TLE1 | GRCh38.p7 | 9:81591072 | AGAATAAACATAATT[C/T]ATTGCTATAATGAAT | 7088 |
rs749044052 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638349 | TAACATTATAAACAC[A/G]AAGTGTCATTTCTAA | 7088 |
rs749046937 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597045 | ACTTTGCTGTTAAAT[A/G]AACCTCTCTCTGGTT | 7088 |
rs749059805 | snp | A/G | 3.34504e-05 | 0.00408951 | intron-variant | TLE1 | GRCh38.p7 | 9:81652167 | ATTAATAAGAAATGA[A/G]AGCTGGTTATACACA | 7088 |
rs749068039 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665593 | ATTCTCTAGCTCCTC[C/G]TGAGGCAGATTGCAG | 7088 |
rs749082394 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657189 | TGTCCTTTGGTGGTG[C/T]TTCCTTGAATGGGAC | 7088 |
rs749102714 | snp | C/T | 1.8739e-05 | 0.00306091 | intron-variant | TLE1 | GRCh38.p7 | 9:81611996 | ACATCATTCAACTGA[C/T]CCACTCCATCAAACC | 7088 |
rs749132736 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676427 | TGAAGTAAACAGGTG[A/G]TGGTGTTTGAACTGG | 7088 |
rs749146645 | snp | C/T | 2.62961e-05 | 0.00362593 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688291 | ACTCAATTCTCCGGT[C/T]AATTTCCAACTTTAA | 7088 |
rs749149501 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609297 | GCCACATTGGCCAGG[C/T]TGGTCTCGAACCCCC | 7088 |
rs749162611 | snp | A/G | 4.4339e-05 | 0.00470824 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688258 | CTCTGGCGGCGGCCG[A/G]GGCTCTGTTCCCCGG | 7088 |
rs749183909 | snp | C/G | | | missense | TLE1 | GRCh38.p7 | 9:81611912 | GGACCATCCCAAAAG[C/G]AGCAGGATATGGGCC | 7088 |
rs749211643 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607562 | ACTTGGCCTTATTTG[C/T]CTGTTATTCCACCAA | 7088 |
rs749246097 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648025 | ACCTGTAATCCCAAC[A/C]CTTTGGGAGGCTGAG | 7088 |
rs749248808 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679834 | AGTTTCTCAGTTTCC[-/T]TCCCCTTTAATCCAC | 7088 |
rs749301264 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651248 | GCACTCACATATGAA[A/T]AAAATCAGAAAGGAC | 7088 |
rs749318353 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634747 | CACGCTGTTTTCAGA[A/G]GGATTAAAATGGGGG | 7088 |
rs749355881 | snp | A/G | 3.33862e-05 | 0.00408558 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687475 | GAGGGACGGGAATGC[A/G]GGCGGATGAATAAAG | 7088 |
rs749362927 | snp | G/T | 6.90632e-05 | 0.00587595 | intron-variant | TLE1 | GRCh38.p7 | 9:81634056 | GCAGCACTGTAAGAG[G/T]ATGAGGACAAAGTCC | 7088 |
rs749371285 | snp | A/G | 6.59957e-05 | 0.005744 | missense, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587739 | AGGTCCCAGGACCTG[A/G]CTGTGTTGTCCAAAC | 7088 |
rs749393803 | snp | C/T | 0.000170833 | 0.00924053 | missense | TLE1 | GRCh38.p7 | 9:81611771 | GACAGCGGCCTACCA[C/T]GGGGGAGCGCCCGTA | 7088 |
rs749415794 | in-del | -/CA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594458 | AACCCTGCATGTTCT[-/CA]CTCATAAATGGGAGT | 7088 |
rs749425226 | snp | A/T | 7.6864e-05 | 0.00619888 | intron-variant | TLE1 | GRCh38.p7 | 9:81610334 | GCAGACTCAGTTTAT[A/T]GCAGCAGGCACTTTG | 7088 |
rs749443972 | snp | C/T | 4.83606e-05 | 0.00491711 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687429 | GCCTGCAGCCTGGTG[C/T]GGCGTCTGGGGGCGA | 7088 |
rs749457830 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603792 | GGATCACCTGAGGTT[A/G]TGAATTCAAGACCAG | 7088 |
rs749466960 | snp | A/G | 1.66034e-05 | 0.00288122 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81620444 | TTAATTACTTACATA[A/G]TGGCTGGAGTCCTTA | 7088 |
rs749535103 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656110 | AGGAAGCCCGTGCAT[G/T]ACCTTGCTTTAGCCA | 7088 |
rs749550636 | in-del | -/TT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661205 | ATATATATATGTATT[-/TT]TATATATATATATAT | 7088 |
rs749573127 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644181 | TTGGAAAACAGTCTG[C/G]CTGTTGCTCAAAAAG | 7088 |
rs749576257 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611582 | TTAATGAAGCAGCAT[C/G]CTGATGAAAGCTGAC | 7088 |
rs749584192 | in-del | -/ATA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630769 | AAATAGATAAGTACT[-/ATA]ATATTTTAGGCACTA | 7088 |
rs749594603 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640668 | ACAGCCACGCATTGA[A/G]AATTTTAATTCACAT | 7088 |
rs749631867 | snp | A/C | 0.0213872 | 0.101174 | intron-variant | TLE1 | GRCh38.p7 | 9:81613563 | GTATTATTTTTAATC[A/C]AAGCCATATTACACA | 7088 |
rs749637636 | in-del | -/TGTGTGT | 1.66125e-05 | 0.00288201 | intron-variant | TLE1 | GRCh38.p7 | 9:81633308 | GTGTGTGTGTGTGTG[-/TGTGTGT]GTGTGTGTGTGCAGC | 7088 |
rs749644598 | snp | G/T | 1.64819e-05 | 0.00287066 | missense | TLE1 | GRCh38.p7 | 9:81593222 | TGAGGGCGTCGGGGG[G/T]AAAAGGGACAGGCTG | 7088 |
rs749646839 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681799 | CCAGTCAGCGGCACT[A/G]CTGATTCTCCTAACT | 7088 |
rs749653168 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653297 | AGATGCATTCATCCC[A/G]TGCACACTTAGAACA | 7088 |
rs749664479 | snp | G/T | 1.64746e-05 | 0.00287002 | missense | TLE1 | GRCh38.p7 | 9:81616041 | AGGCCGTGGAAGCTG[G/T]ACTGCTAGAAGCATC | 7088 |
rs749676480 | in-del | -/A | 1.64991e-05 | 0.00287215 | intron-variant | TLE1 | GRCh38.p7 | 9:81615965 | AAACAGGCAAGTGTC[-/A]AGTTTTCTTTACCTA | 7088 |
rs749677069 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610362 | TTGTGAACATCAATA[C/G]TGTTCATTAGAAACT | 7088 |
rs749684284 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666136 | AGAGCCTGTTCACAG[A/G]AAATGGTATTGACTT | 7088 |
rs749721296 | snp | A/G | 0.000111788 | 0.00747539 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634188 | CAGCGCAAGAAGGCC[A/G]GCACTGCCCCCGAGG | 7088 |
rs749757632 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662061 | GTTCAAATGAAAAGC[A/C]TTCCATGCATGAAGC | 7088 |
rs749798894 | snp | A/C | 0.00018784 | 0.00968941 | intron-variant | TLE1 | GRCh38.p7 | 9:81590776 | TGCTAAAGAAGCGAA[A/C]CCCTCCTTAGACGAC | 7088 |
rs749819697 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585180 | CTCATAATGACTTCC[A/G]CTGCCCCTGCTCCAT | 7088 |
rs749858575 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636140 | TTCATAGCATTCTTG[G/T]AAAGTATAAACTACT | 7088 |
rs749872707 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623202 | TGCATTTCTTGAGGT[A/G]TTTTTCCCTCATGTT | 7088 |
rs749886539 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612502 | TGGGGAATATCAGGT[A/T]GCAAATTATGAGTTT | 7088 |
rs749891021 | snp | A/C | 1.80292e-05 | 0.00300238 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587675 | AGGCGGAAGCCACTC[A/C]GTCACCTGGGAGGTG | 7088 |
rs749903127 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653813 | TTCTACAGTGTGCCC[A/T]CAGATGTGTTGGATA | 7088 |
rs749932234 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688126 | GGCGAGAAGGTCCGC[C/T]GGGCCTCAGAAGCCA | 7088 |
rs749952983 | snp | C/T | 2.22625e-05 | 0.00333628 | missense, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687403 | TCCGGGATAGTGAAC[C/T]TGAAGGGCTGGCCTG | 7088 |
rs749964211 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664795 | AACTCCAGCGTACAC[A/G]AGGATGGTCTTGTGC | 7088 |
rs749979007 | snp | A/G | 0.000111012 | 0.00744942 | intron-variant | TLE1 | GRCh38.p7 | 9:81611730 | AATGGAGCATGCAGC[A/G]TTCCTACCCCAACCA | 7088 |
rs750000982 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588977 | AATTCTAAGCCAAGA[C/T]GTGAACCATCACTTT | 7088 |
rs750071611 | in-del | -/GAGA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607078 | AAAAAAAAAAAAATG[-/GAGA]GAGAGAGAGATTTTA | 7088 |
rs750108197 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663094 | CAAATTATCCACACG[C/T]CTCGGCCCCCCAAAG | 7088 |
rs750120337 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620321 | ACAATGTAAGAACCT[C/T]TCCTCTTTACAGTAT | 7088 |
rs750147959 | snp | C/G | 1.64874e-05 | 0.00287113 | intron-variant | TLE1 | GRCh38.p7 | 9:81616740 | TTTACTAAAAGCTAA[C/G]AATAGGTTTGAGGCA | 7088 |
rs750153747 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632607 | TTTGCTACACAACAT[C/T]TGAGACACACTTTAA | 7088 |
rs750180390 | in-del | -/CA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668607 | CTCCAAGATAACAAT[-/CA]CAACCTACTTTCAGG | 7088 |
rs750184866 | snp | A/G | 3.29462e-05 | 0.00405857 | missense | TLE1 | GRCh38.p7 | 9:81593189 | TCTGGCGAGCATGCC[A/G]GGGGATTCCGGGTCC | 7088 |
rs750196333 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680330 | AAAGGCAGAAAGAGG[C/G]GGAGGCAAGGGAGGT | 7088 |
rs750206113 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671576 | CTTGAACCCGGGAGG[C/T]GAAGCTTGCAGTGAG | 7088 |
rs750216605 | snp | A/G | 3.32878e-05 | 0.00407956 | intron-variant | TLE1 | GRCh38.p7 | 9:81613544 | CATTAAACAAATTAA[A/G]TGAGTATTATTTTTA | 7088 |
rs750241995 | in-del | -/ATA | 4.94303e-05 | 0.00497119 | cds-indel | TLE1 | GRCh38.p7 | 9:81584189 | TAAACGTTAAACCAC[-/ATA]ATGTTTTCAGTAGAT | 7088 |
rs750247177 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592396 | CGAACATGTCCCAAC[A/G]TGTTTTATGTCCCTG | 7088 |
rs750259518 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683610 | TTCAAATGTAAGTCC[A/T]CTTTAAACTGAATTA | 7088 |
rs750274799 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658195 | AGGATTTATAATCCT[A/G]GCATGAGCCACTGTG | 7088 |
rs750346780 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592081 | AATCGGAACATGGCC[A/G]GGCGCGGTGGCTCAC | 7088 |
rs750347761 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631912 | GTTCCAGACCAGCCT[A/G]ACCAACATGGAGAAA | 7088 |
rs750356604 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601975 | AGCAGATAGAAACAC[G/T]GCTTGTACACGATTA | 7088 |
rs750386616 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622647 | GCGGCTTAAATGAAG[C/T]TTATAATCTGAATAG | 7088 |
rs750418477 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642301 | TTTTTCAGATTTTTA[A/T]ATATTTGCAATATTC | 7088 |
rs750426412 | snp | C/T | 0.000148281 | 0.00860922 | missense | TLE1 | GRCh38.p7 | 9:81613443 | GGAGGCCTGGAGTGG[C/T]GCTGGTGCCCGGCGT | 7088 |
rs750432123 | in-del | -/A | 5.66588e-05 | 0.00532224 | intron-variant | TLE1 | GRCh38.p7 | 9:81610326 | AGGCATTGCAGACTC[-/A]AGTTTATTGCAGCAG | 7088 |
rs750433290 | in-del | -/CACACG/CACC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652113 | GTTAAGATACACACA[-/CACACG/CACC]CACACACACACACAC | 7088 |
rs750443388 | snp | C/T | 9.68335e-05 | 0.00695754 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688283 | CCCCGGCAACTCAAT[C/T]CTCCGGTCAATTTCC | 7088 |
rs750473416 | snp | C/T | 5.07074e-05 | 0.00503499 | intron-variant | TLE1 | GRCh38.p7 | 9:81620955 | GACATATTCTTTAAC[C/T]GTAAGAGTCAATGTG | 7088 |
rs750486468 | snp | A/C | 1.83758e-05 | 0.0030311 | intron-variant | TLE1 | GRCh38.p7 | 9:81611968 | CCAGCTGCTGAAAGG[A/C]AACACAAGCCGCACA | 7088 |
rs750489516 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629513 | GTTCATCCCTTTCAG[A/G]AATAAGAAACTTTAA | 7088 |
rs750504926 | snp | C/T | 1.70116e-05 | 0.00291642 | missense | TLE1 | GRCh38.p7 | 9:81611879 | GGCTGGTCAGCTCGC[C/T]GTTCATGCCAGCGTG | 7088 |
rs750520507 | in-del | -/CAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617133 | GATTACTAGTTAATG[-/CAA]AAAAAAAAAAAAAAA | 7088 |
rs750574901 | snp | C/T | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589913 | CGCAGGGACCGGGCC[C/T]GGCTCAATGACACTT | 7088 |
rs750588878 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679422 | GTTAAATCAGGTGAA[C/T]GGCAATACATGAATA | 7088 |
rs750610036 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639051 | CCTCAGGCTCCTAAG[A/T]ACATACTTAGCTGGG | 7088 |
rs750631915 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598318 | CAAACTGTTCCCTCC[C/T]GCTAGAACAGCACCG | 7088 |
rs750654166 | in-del | -/TAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623617 | AACCCCATCTGTACT[-/TAA]AAAAAAAAAAAAAAA | 7088 |
rs750667723 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609349 | CTCAGCCTCCCAAAG[A/T]GCTAGGATTATAGGC | 7088 |
rs750691074 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | TLE1 | GRCh38.p7 | 9:81584221 | TGACTTCATAGACTG[C/T]AGCCTTCTTGTCCCC | 7088 |
rs750716271 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639359 | CGTAAGCTACCATAG[C/T]TGGCCTGCATCTGTA | 7088 |
rs750794082 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675574 | AAAACTCCTCACTAA[A/G]AACTCTCAGTGGTTA | 7088 |
rs750824614 | snp | A/G | 6.595e-05 | 0.00574201 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81652210 | GACCTGGTAGGCCAC[A/G]TACCCCGATGATGGC | 7088 |
rs750854770 | in-del | -/GTGTGTGTGT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633291 | TCAGAAGGGGACCGT[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 7088 |
rs750872224 | in-del | -/GTGTGTGTG | 6.90954e-05 | 0.00587732 | intron-variant | TLE1 | GRCh38.p7 | 9:81633305 | TGTGTGTGTGTGTGT[-/GTGTGTGTG]TGTGTGTGTGTGCAG | 7088 |
rs750891615 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604367 | AACCATGGCCCACAA[C/G]AGAGGGCTGAAGCGA | 7088 |
rs750900418 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685546 | CCATCAATCCACAGG[A/C]CAGGAAACCAAGGCA | 7088 |
rs750914599 | snp | C/T | 0.0176297 | 0.0922174 | intron-variant | TLE1 | GRCh38.p7 | 9:81652140 | ACACACACACACACG[C/T]AAAGCCATCAAATTA | 7088 |
rs750938361 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618163 | TTATACAATGTAGGC[A/G]TATGGAAAAAGCAGG | 7088 |
rs750973191 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637988 | AGATTTCTCCTGTAA[-/C]CCCAGCAGCTCAATC | 7088 |
rs750998325 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656711 | CAGGGACACCATCCC[A/T]GTCAATACAGATTAA | 7088 |
rs751000262 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644919 | GAATCGTTTGAACCC[A/G]GGAAGCGGAGGTTGC | 7088 |
rs751044589 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651769 | CTTTTACTAGACTAA[C/T]GAAGCAAGGGTGGTT | 7088 |
rs751061736 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661650 | GTGTCTGGCAACAGA[C/T]ACATGGGCAAGAACA | 7088 |
rs751064691 | snp | A/G | 0.000137228 | 0.00828221 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634231 | GGAGGCTGAAGTCCC[A/G]AAGGGTGAGGCGTAA | 7088 |
rs751073686 | snp | C/T | 1.66891e-05 | 0.00288864 | intron-variant | TLE1 | GRCh38.p7 | 9:81613551 | CAAATTAAATGAGTA[C/T]TATTTTTAATCCAAG | 7088 |
rs751079055 | snp | A/C | 5.83323e-05 | 0.00540025 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688200 | TGGCCCCCCACCACC[A/C]CCCAGCCGCGCCTCA | 7088 |
rs751081284 | snp | C/T | 0.000394017 | 0.0140304 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634155 | TGCCAAGTGAGACTG[C/T]CCACTCAGAGCACTA | 7088 |
rs751104407 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652615 | TGGAAGATCACCCTT[A/G]TTCACAAAAGGGGTT | 7088 |
rs751106595 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674529 | ATCACGACAATTCCA[C/T]ACACACAAAGTTCAA | 7088 |
rs751128163 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669311 | CCATCTGTCTAATAG[-/A]ACATGTGGATAAAAA | 7088 |
rs751140133 | snp | C/T | 6.6527e-05 | 0.00576707 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587847 | ATAAAACAAACCAGA[C/T]TGAATAATGATTTCC | 7088 |
rs751220333 | in-del | -/TCCCTTTTTTTTTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632472 | TTTAAATGTTCAGTA[-/TCCCTTTTTTTTTTT]TTTTTTTTTTACCAT | 7088 |
rs751246425 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81635634 | ATTCTGATTTGTGCT[A/C]ACTTCCTTGGGACTC | 7088 |
rs751276295 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631107 | TCCAAAACACATAAA[C/T]CCACATTTGAACTAG | 7088 |
rs751293312 | snp | C/G/T | 8.04916e-05 | 0.00634352 | missense | TLE1 | GRCh38.p7 | 9:81611804 | CCACCACGGCGGCCG[C/G/T]GGCGGCTGCGGCGCT | 7088 |
rs751299466 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634578 | CATCTACACTGTCAC[C/T]TTCTGGTATCACTCA | 7088 |
rs751316288 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642168 | AATTGGTACAGCCCT[A/G]ATGCAAAACAACAGT | 7088 |
rs751343916 | snp | C/T | 2.28245e-05 | 0.00337813 | intron-variant | TLE1 | GRCh38.p7 | 9:81593313 | AAGACAGAAAACACA[C/T]TTACAGAGGAAGCAA | 7088 |
rs751368214 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600586 | CCCACATGGCAATAA[C/T]AAGGAACAAAATGGG | 7088 |
rs751371474 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641146 | CCAAATCACTCTTCC[C/T]TGATTTCTGCTATTT | 7088 |
rs751434254 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669377 | AATCCGTGGCACAAG[C/T]CAGGAACCAGTTAAA | 7088 |
rs751459936 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681479 | CGCTTGAACCTGGGA[A/G]GCGGAGGTTGCAGTG | 7088 |
rs751469443 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639688 | CCCGGGTTCAAGCTA[C/T]TCTTTGTGCCTCAGC | 7088 |
rs751474138 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664511 | GAGTAGCTTTTGTTT[A/G]AAATATAATTATGCC | 7088 |
rs751499189 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | TLE1 | GRCh38.p7 | 9:81616004 | ATTTCTTTGGATTTC[A/G]AAGAAGTGGAACTTG | 7088 |
rs751535248 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611219 | GCAGGGCAAACAGAC[A/G]AGAGACAGCCTGCCC | 7088 |
rs751544614 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588601 | AATCGCCATCAGAAA[C/T]GATCAGCCAACAGGG | 7088 |
rs751545706 | in-del | -/AAAAAAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623618 | ACCCCATCTGTACTT[-/AAAAAAAA]AAAAAAAAAAAAAAA | 7088 |
rs751565642 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652883 | ATCTTGACCCACCAG[G/T]CATTTTCGGAAACTC | 7088 |
rs751615188 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679077 | CACCTGAACCCAGGA[A/G]GCGGAGGCTGCAGTG | 7088 |
rs751617130 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666505 | TGTGTAGCCAGGCGC[A/G]GTGGCTCACACCTGT | 7088 |
rs751618285 | snp | G/T | 0.000115425 | 0.00759599 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81613402 | AACGAGGGGGTCTAT[G/T]GCTGGAGGCTTGCCG | 7088 |
rs751621536 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627193 | TCCACCTATGTCCCA[A/G]TGAGGAAATGATAAA | 7088 |
rs751639870 | snp | G/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690691 | TCTCAGCTACAAGAC[G/T]ACGAGTCTGTTTCCA | 7088 |
rs751641283 | in-del | -/TGTA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624753 | CTGAGGTTTCTAGAC[-/TGTA]TGTAAGTTTTCATTT | 7088 |
rs751652477 | in-del | -/AGC | 1.73674e-05 | 0.00294676 | cds-indel | TLE1 | GRCh38.p7 | 9:81611913 | GACCATCCCAAAAGG[-/AGC]AGGATATGGGCCGGG | 7088 |
rs751663676 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636848 | TCTCTACTAAAAATA[C/G]AACAATAAGCCAGGT | 7088 |
rs751669814 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659698 | ATACAGTTAGCCCTC[A/G]TCATCCAAAAATTAG | 7088 |
rs751670458 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678107 | TAAAATAAATAGCTG[C/T]TTTTTATACCTACTA | 7088 |
rs751695165 | snp | C/T | 3.32928e-05 | 0.00407987 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81591020 | GCAGCCATCGGGTAG[C/T]AATTTACAGGAACGG | 7088 |
rs751702743 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650031 | TATGCCCAAGACACA[C/T]AATGGGCCTAAGTCT | 7088 |
rs751717681 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597623 | CCTCAGAACTGAGAC[C/T]CAGCCCCCACCTAGC | 7088 |
rs751773169 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81608217 | GCCTCACAACTTTAC[C/T]GGTTTGCCCCTTATC | 7088 |
rs751777505 | in-del | -/G | 0.000110114 | 0.00741922 | intron-variant | TLE1 | GRCh38.p7 | 9:81633303 | CGTGTGTGTGTGTGT[-/G]TGTGTGTGTGTGTGT | 7088 |
rs751788463 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656849 | AAATACGCCTCCACA[C/T]AGATCTCTAAAAGGA | 7088 |
rs751862569 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603570 | ATTTCCACAAATAAA[C/G]TTACCAAAATAACCT | 7088 |
rs751862587 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616831 | GGCCTGCAGGCTCTC[C/T]ATCAGTTTGCCAGTC | 7088 |
rs751889262 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673116 | CGACTCTACTAAAAA[A/T]ACAAAAATCAGCTGG | 7088 |
rs751897001 | snp | A/G | 4.47517e-05 | 0.0047301 | missense, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687407 | GGATAGTGAACTTGA[A/G]GGGCTGGCCTGCAGC | 7088 |
rs751959792 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685481 | TCTCCCTCTCCTAGT[A/C]ATTTAAACACTTGTA | 7088 |
rs751973708 | snp | G/T | 1.64898e-05 | 0.00287135 | intron-variant | TLE1 | GRCh38.p7 | 9:81616748 | AAGCTAAGAATAGGT[G/T]TGAGGCACAGTTAGA | 7088 |
rs752011764 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684776 | TTTCTAAAAGACTTA[C/T]TGTACCAGCGTCTTG | 7088 |
rs752015626 | in-del | -/ACAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649734 | CTGCTGCTTGTAGGA[-/ACAG]ACAGTTTCCCGGTAC | 7088 |
rs752036814 | snp | A/G | 1.65209e-05 | 0.00287405 | intron-variant | TLE1 | GRCh38.p7 | 9:81584355 | GGAACAACGGTACTC[A/G]GAGGCCCTGCTCCCT | 7088 |
rs752039788 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598279 | CCTAAAATATCACAT[A/G]CTGTCACATCTCCAA | 7088 |
rs752063671 | snp | A/T | 1.648e-05 | 0.0028705 | missense | TLE1 | GRCh38.p7 | 9:81616677 | ACAACTAAGTTGTCA[A/T]CGCTTTTGTCACCAT | 7088 |
rs752066127 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607062 | ACCCAGTGTCTCTAA[-/A]AAAAAAAAAAAAATG | 7088 |
rs752092603 | snp | C/T | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589898 | GCACTGTCACCCACA[C/T]GCAGGGACCGGGCCC | 7088 |
rs752113046 | snp | A/C | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589367 | AGGCACATCCTATGA[A/C]TGTTCAGAACGTGCT | 7088 |
rs752158265 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633007 | TACAGTCAACCAGAC[C/T]TAGAATGCAACCATT | 7088 |
rs752183946 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674447 | ACACTGGGGTCCTCA[A/C]TGAGGTTTTGTTTCT | 7088 |
rs752193991 | snp | G/T | 1.65353e-05 | 0.00287531 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616119 | GGGCAGGGCTTGCTC[G/T]CGGAGAAGAAGGGTC | 7088 |
rs752204237 | snp | A/G | 3.29495e-05 | 0.00405877 | missense | TLE1 | GRCh38.p7 | 9:81616022 | GAAGTGGAACTTGCC[A/G]AGGAGGCCGTGGAAG | 7088 |
rs752205381 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593684 | CCCTGCTAAAGATGA[A/G]GCCCTTAAGAACTAA | 7088 |
rs752231542 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649575 | TAATAGATGTCTAAA[A/C]CGTTAAATTACTATT | 7088 |
rs752233268 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626135 | AAATAAAGCACATTA[C/T]TCAAATGGATTTCTT | 7088 |
rs752258401 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603145 | AGCCCCTTCCCCTAT[C/T]GGGTTAGTGCAGCTC | 7088 |
rs752341379 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586018 | GTGTCGTTAGGTGAC[-/TTT]TTTTTTTTTTTTTTT | 7088 |
rs752365730 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615424 | TCCCCCAAGTAAGAC[A/G]GCAATGAGGCTGGGC | 7088 |
rs752373040 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610755 | CTGCCCCCCCTCCCA[C/T]CCCCAGTTATGATAA | 7088 |
rs752385330 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640130 | ACAGGACAGCCCTCA[C/T]CACAGAGAATTATCC | 7088 |
rs752414209 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602143 | ATACTTCAACAGAAA[A/G]AGACCAGTGAGAAGG | 7088 |
rs752436193 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651651 | AAAGGCAAAAAGCAA[A/G]GATAACTAAATGAAA | 7088 |
rs752454611 | snp | A/C | 1.65037e-05 | 0.00287256 | missense | TLE1 | GRCh38.p7 | 9:81585582 | GGCTTGTTCACGTGC[A/C]GCACCTCCACATTGC | 7088 |
rs752460555 | snp | A/G | 3.29587e-05 | 0.00405934 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590885 | GACCTTGGAATCGGG[A/G]CTGATGGCCAGGGCG | 7088 |
rs752467586 | snp | C/G | 1.67933e-05 | 0.00289765 | intron-variant | TLE1 | GRCh38.p7 | 9:81585671 | CTACAAGGAGCAAGA[C/G]AGGCTCACTCATTAT | 7088 |
rs752469892 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661918 | AGTGGAACAATCATA[C/T]GTTACTGATGACATT | 7088 |
rs752487386 | snp | G/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586513 | AGTAAAAATATAGTA[G/T]TATAATCTTAAGGGA | 7088 |
rs752529783 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681258 | ATTTATTTTTAAATG[C/T]TTCACCATCGGCCGG | 7088 |
rs752532004 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633301 | ACCGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 7088 |
rs752552540 | snp | C/T | 5.00889e-05 | 0.00500419 | intron-variant | TLE1 | GRCh38.p7 | 9:81620605 | TCCCAAGCCTCTTTG[C/T]ACACATGAAACCCAA | 7088 |
rs752554163 | snp | C/G | 4.54742e-05 | 0.00476813 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687290 | TGGGTGCAAGGGGCA[C/G]CGGGACGCCCGCGAC | 7088 |
rs752568524 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679559 | TGCGCATCCTAGTTC[C/T]ACTTAAAACATCACA | 7088 |
rs752594591 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659969 | CATAACGCCAATAAA[C/T]GCACTCTTCTCTAGG | 7088 |
rs752594697 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684881 | CTACTCAATCGAGGG[G/T]CCTTTGGGCTGAGCA | 7088 |
rs752599148 | in-del | -/AACTCCA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653013 | CACCTCCCAACTCCC[-/AACTCCA]CCCACAAATAAAAAC | 7088 |
rs752610068 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604453 | CTGAAGAGCTGCCAT[A/G]AGGATGATAGATTAG | 7088 |
rs752638140 | snp | G/T | 1.64999e-05 | 0.00287222 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685814 | TGAAAAAGGAAAAAG[G/T]CCAATCTTTGATACC | 7088 |
rs752684376 | snp | A/G | 0.00070936 | 0.0188196 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611805 | CACCACGGCGGCCGC[A/G]GCGGCTGCGGCGCTC | 7088 |
rs752686736 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661408 | GCTGTTTGAAGCTCA[A/G]AACAGGGTGAGGACT | 7088 |
rs752687336 | in-del | -/TT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660257 | TCAATGAACCAAAAC[-/TT]AATCTCCATGCACCC | 7088 |
rs752687407 | in-del | -/AAC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618028 | AAGACTCCGTCTCAA[-/AAC]AACAACAACAACAAA | 7088 |
rs752710222 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676982 | TGGCTCACGCCTATA[A/T]TCCCAACACTTTGGG | 7088 |
rs752712165 | snp | A/C | 1.68567e-05 | 0.00290312 | intron-variant | TLE1 | GRCh38.p7 | 9:81620427 | ATATTATTTCAAGTC[A/C]TTTAATTACTTACAT | 7088 |
rs752733363 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650354 | TGCCATCATGAAATT[A/G]TATGTCGTAATGTAG | 7088 |
rs752740736 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | TLE1 | GRCh38.p7 | 9:81593179 | AGGGTGTTGATCTGG[C/T]GAGCATGCCGGGGGA | 7088 |
rs752745806 | in-del | -/TTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683222 | TTCCCCATCACTGCA[-/TTT]TTTTTTTTTTTTTTT | 7088 |
rs752770151 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637129 | TTGGGAGGCTGAGGC[A/G]GGTGTAACACTTGAG | 7088 |
rs752772343 | snp | C/T | 1.65932e-05 | 0.00288034 | intron-variant | TLE1 | GRCh38.p7 | 9:81654064 | AGCCACACAAATGTT[C/T]AGAATACTTCACAAT | 7088 |
rs752790304 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655207 | CGTCTCTACTCAAAA[C/T]ACAAAAATTAGCCGG | 7088 |
rs752806476 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596122 | TTAAATAGATGCACC[C/G]AGTAACAGACGGGAG | 7088 |
rs752826983 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647757 | AGGTCATAAAGCTAA[C/T]AGATGGCAGCTAAGT | 7088 |
rs752828339 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659034 | CTTCCTCAGCCTCGC[A/G]AGTAGCTGGGATGAC | 7088 |
rs752839694 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | TLE1 | GRCh38.p7 | 9:81584272 | TATCATCCACAGAGA[C/T]GTCACAGCTAAGCAC | 7088 |
rs752866911 | in-del | -/ACTA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628742 | ATGGTCGCTCAGATT[-/ACTA]ACTAACTCTCAATCT | 7088 |
rs752897495 | in-del | -/CGGCGGCCG | 2.16074e-05 | 0.00328683 | cds-indel | TLE1 | GRCh38.p7 | 9:81611795 | GCCCGTAGGCCACCA[-/CGGCGGCCG]CGGCGGCTGCGGCGC | 7088 |
rs752916210 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677518 | TGCAGTGAGCTGAGA[G/T]CATGCCACTGCACCC | 7088 |
rs752917424 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591927 | TTACAATTTTCCAGG[C/G]AGGCAGTGGGTACGT | 7088 |
rs752971683 | snp | C/T | 1.93239e-05 | 0.0031083 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688211 | CACCACCCAGCCGCG[C/T]CTCACCGGGTGCCGG | 7088 |
rs752987753 | in-del | -/ATT | 1.68775e-05 | 0.0029049 | intron-variant | TLE1 | GRCh38.p7 | 9:81585682 | AAGACAGGCTCACTC[-/ATT]ATTCCGCCTGATACA | 7088 |
rs752997358 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627947 | ACCAAGGCTGGGTGC[A/G]GTGGCTCACGCCTGT | 7088 |
rs753010397 | snp | C/G | 1.64879e-05 | 0.00287118 | missense | TLE1 | GRCh38.p7 | 9:81613508 | TTCAGAACAGGCGTG[C/G]TGGCTTTTTCATGCT | 7088 |
rs753017264 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631878 | GAGGCTGAGGCAGGC[A/G]GATCACCTGAGGTTG | 7088 |
rs753103328 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683924 | TAAAGAAGAGGTCAT[C/T]CCGCCACATAACCTA | 7088 |
rs753115459 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670879 | AAATTAGTCAAGAAA[C/T]AAGGATGGGCTGGGT | 7088 |
rs753121262 | snp | A/C | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588316 | AGCATTCCTGTTTCC[A/C]TGAGTGAATCAACAC | 7088 |
rs753136486 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677774 | TTCAAACACACCTAC[A/G]TTCTCAAAGACTGAT | 7088 |
rs753142113 | snp | C/T | | | missense | TLE1 | GRCh38.p7 | 9:81613479 | TGTCGCTCCGAGGCG[C/T]TGGTGTGCTGGATTT | 7088 |
rs753168671 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589240 | TAACTCATGAAACGC[C/T]GTTCCTCCTTGACTG | 7088 |
rs753182297 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638045 | GGGCAAAGCCATTCT[C/G]TACTGAGACTTCGCA | 7088 |
rs753185459 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626835 | GGCCCTTCTACCCTC[C/G]TCCAGGCAAAACAAA | 7088 |
rs753188701 | snp | A/C/T | 0.000140471 | 0.00837965 | intron-variant | TLE1 | GRCh38.p7 | 9:81611761 | CAGCCCACCCGACAG[A/C/T]GGCCTACCATGGGGG | 7088 |
rs753228129 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611377 | CCTAAGGTTTAATGA[-/G]GAAAAAAAAAGTTCA | 7088 |
rs753283625 | snp | C/T | 1.65083e-05 | 0.00287296 | missense | TLE1 | GRCh38.p7 | 9:81585594 | TGCAGCACCTCCACA[C/T]TGCTGCTCTCCATGC | 7088 |
rs753299284 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81620501 | ATTGGAAAATTCAGG[C/T]CCATTTCTGCGTTTA | 7088 |
rs753344999 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602096 | GCTTCATGAAGGAGG[C/T]AGCAACTCAAGTGGG | 7088 |
rs753358188 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623011 | TTGCCCCTGACTTCT[A/T]CCAGCCCTGACGCTG | 7088 |
rs753358783 | snp | C/G | 4.46598e-05 | 0.00472524 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687296 | CAAGGGGCACCGGGA[C/G]GCCCGCGACCACTCG | 7088 |
rs753373843 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683760 | TTTCAAATTGCTAAG[A/C]CAATTATACACAGCA | 7088 |
rs753375787 | snp | A/G | 1.74683e-05 | 0.00295531 | intron-variant | TLE1 | GRCh38.p7 | 9:81600129 | CTCCTAAACAGGACA[A/G]AGATACAAATGGAGA | 7088 |
rs753398190 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655053 | TGTCCTTAGTGTCTA[C/T]AGCACGGGCTGTTTT | 7088 |
rs753467424 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647197 | TGTGGACGGGAGGAC[A/G]GTCCCCACTGGTCAT | 7088 |
rs753486700 | snp | A/G | 3.31461e-05 | 0.00407086 | missense | TLE1 | GRCh38.p7 | 9:81616125 | GGCTTGCTCGCGGAG[A/G]AGAAGGGTCCTCAAC | 7088 |
rs753494574 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588188 | AATAAAAGACAAACA[C/T]ACAAAATCCCGATTG | 7088 |
rs753506085 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667911 | GCTCACACCTGTAAC[C/T]CCAGCATTTTGGGAG | 7088 |
rs753535907 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661862 | GTTAAGGCAATTTTT[-/A]AAAAATTAACAAAAT | 7088 |
rs753668842 | snp | C/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690425 | CGACTGTGATGTCCT[C/T]CCACCCCACCCACCC | 7088 |
rs753672162 | snp | C/G | 2.27472e-05 | 0.0033724 | missense, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687378 | TTCCTCTTTAATCCG[C/G]TCCAGGGACTCCGGG | 7088 |
rs753675090 | snp | A/C/G | 4.94645e-05 | 0.00497291 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81613417 | GGCTGGAGGCTTGCC[A/C/G]AGACCTGGACGGAGG | 7088 |
rs753693601 | snp | C/T | 3.29775e-05 | 0.0040605 | intron-variant | TLE1 | GRCh38.p7 | 9:81633380 | CTGCTCCCGAGGTTA[C/T]CAAGAAACGCACAGA | 7088 |
rs753754965 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593319 | GAAAACACATTTACA[A/G]AGGAAGCAATCCCTA | 7088 |
rs753781487 | snp | A/G | 2.35325e-05 | 0.00343011 | intron-variant | TLE1 | GRCh38.p7 | 9:81633321 | TGTGTGTGTGTGTGT[A/G]TGTGCAGCAGGCGTT | 7088 |
rs753806203 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593519 | TAAAATTTTTTAAGG[G/T]TTTTAAATTGTTCTT | 7088 |
rs753837577 | snp | A/T | 1.68162e-05 | 0.00289962 | intron-variant | TLE1 | GRCh38.p7 | 9:81585676 | AGGAGCAAGACAGGC[A/T]CACTCATTATTCCGC | 7088 |
rs753844268 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599274 | AGTAAGCGGTAGACC[A/T]ACTCCAGCTCAGCCC | 7088 |
rs753848590 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686510 | TCAATAATGAGAAAG[C/T]CCCTGACAAAGTAAG | 7088 |
rs753850828 | snp | C/G/T | 0.000168442 | 0.00917587 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611811 | GGCGGCCGCGGCGGC[C/G/T]GCGGCGCTCATCTGG | 7088 |
rs753852163 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632778 | TTACTGGTATGCTCA[A/G]TTCTTATGTCTAAAA | 7088 |
rs753859629 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603092 | CAGCGTGAAGTCACC[C/G]GGCCTTTGCACATGC | 7088 |
rs753871283 | snp | A/T | 1.65081e-05 | 0.00287293 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685790 | GCTAACACGTTTGCT[A/T]ATATCATATGAAAAA | 7088 |
rs753874728 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659276 | GTTAACCTGGGTATT[G/T]GACCCTGCTGCCTTC | 7088 |
rs753890372 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646322 | CGGACTGCGAAGACT[C/T]CTTTGCAATATTGCT | 7088 |
rs753919426 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | TLE1 | GRCh38.p7 | 9:81620517 | CCATTTCTGCGTTTA[C/T]CTGTGCCTCTTAGAC | 7088 |
rs753926304 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677288 | TAAACAACTCAGGCC[A/G]GGCGCAGTGGCTCAC | 7088 |
rs753995305 | snp | A/C | 3.3295e-05 | 0.00408 | intron-variant | TLE1 | GRCh38.p7 | 9:81584557 | ATATCTAGTTTTCAC[A/C]AGGTTAAAATTCCTA | 7088 |
rs754008588 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653404 | GTCAGTTTCATAGAT[A/T]ACTCATATAAAGAGA | 7088 |
rs754013655 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595984 | ACAAATCAAGCTGGG[C/T]GCCTCCAGGTAAGGC | 7088 |
rs754029205 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669301 | AATTTTCATCTCCAT[C/T]TGTCTAATAGACATG | 7088 |
rs754036610 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591135 | GGCTGTCTTGGTTTT[C/T]TGAGTTAAGAGTGGT | 7088 |
rs754047337 | snp | A/G | 1.71375e-05 | 0.00292719 | intron-variant | TLE1 | GRCh38.p7 | 9:81685631 | GTATTATTAAATCAT[A/G]TGAACTGATGTCTCA | 7088 |
rs754082988 | snp | A/G | 1.65677e-05 | 0.00287812 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590999 | TTCCCCTCCCACTAT[A/G]AGAGTGCAGCCATCG | 7088 |
rs754101710 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617443 | TGGCTCACGCCTGTA[A/C]TCCCAGCACTTTGGG | 7088 |
rs754127054 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641046 | GCTAAGAGTGACAGT[A/G]AGTGGCATTTATAGC | 7088 |
rs754136309 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595406 | TTGAAGAATGCTCAA[C/T]GAACAAAGTCCAGTA | 7088 |
rs754140799 | in-del | -/AAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615713 | GTGAGACTCCGTCTC[-/AAAA]AAAAAAAAAAAAAGA | 7088 |
rs754150005 | snp | A/G | 1.69677e-05 | 0.00291266 | intron-variant | TLE1 | GRCh38.p7 | 9:81652135 | CACACACACACACAC[A/G]CACGTAAAGCCATCA | 7088 |
rs754150410 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687501 | TAAAGCAGTAAGTCA[A/G]AGAAGGCAAGAACGG | 7088 |
rs754150625 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629835 | ACACTTAGGGGACCA[C/T]CATCATATATGCAAT | 7088 |
rs754154602 | snp | A/G | 2.03172e-05 | 0.00318719 | intron-variant | TLE1 | GRCh38.p7 | 9:81593295 | GGAAAAACGATTGGA[A/G]AGAAGACAGAAAACA | 7088 |
rs754190392 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625200 | AAAATCTGGAATTCT[C/G]TGAGAACACCAGATC | 7088 |
rs754234682 | in-del | -/AAAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666784 | TCTCACAAAATAAAT[-/AAAT]AAATAAATAAATAAA | 7088 |
rs754245804 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688316 | CTTTAATCCCGCCGA[A/G]GAAAATTAAGCCGGA | 7088 |
rs754245900 | snp | G/T | 0.000105114 | 0.00724885 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634255 | GGCGTAAGGGGAACT[G/T]GGGGTCCGTGGCCAT | 7088 |
rs754249605 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676931 | AGTGTAATACAACAA[C/T]GTATGTATGTAACTT | 7088 |
rs754269453 | snp | C/T | 4.69032e-05 | 0.00484246 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688277 | TCTGTTCCCCGGCAA[C/T]TCAATTCTCCGGTCA | 7088 |
rs754273449 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663447 | AACTCGGCCCTGCCT[A/G]CAAAGCAACGCAGCT | 7088 |
rs754288818 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596789 | ACTGCAAGGGGCATG[A/G]GAGGGGTTTCTGGGC | 7088 |
rs754300907 | in-del | -/C | 5.73806e-05 | 0.00535602 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688187 | CCCCAACGATCCTGG[-/C]CCCCCCACCACCACC | 7088 |
rs754308218 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673384 | GAAATAAAACACGGT[-/A]AATGGGAAAATCAGT | 7088 |
rs754314656 | in-del | -/GT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633289 | TGTCAGAAGGGGACC[-/GT]GTGTGTGTGTGTGTG | 7088 |
rs754327948 | in-del | -/ACGT | 1.69895e-05 | 0.00291452 | intron-variant | TLE1 | GRCh38.p7 | 9:81652137 | CACACACACACACAC[-/ACGT]AAAGCCATCAAATTA | 7088 |
rs754384300 | snp | A/G | 1.69229e-05 | 0.00290881 | missense | TLE1 | GRCh38.p7 | 9:81611863 | GCGTAGGCAGCGCCT[A/G]GGCTGGTCAGCTCGC | 7088 |
rs754442302 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632865 | GGAAACCTAGCAACC[A/G]AGATGCATTCACAGA | 7088 |
rs754482572 | in-del | -/AAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629730 | CATGTTACTGTCCTG[-/AAT]ATTACAGGCAGCTAC | 7088 |
rs754490152 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592507 | GTTGATGGCTGCCCC[G/T]GGTCTTTGCAGTGAC | 7088 |
rs754521670 | snp | A/T | 1.64727e-05 | 0.00286986 | intron-variant | TLE1 | GRCh38.p7 | 9:81613553 | AATTAAATGAGTATT[A/T]TTTTTAATCCAAGCC | 7088 |
rs754523382 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602097 | CTTCATGAAGGAGGT[A/G]GCAACTCAAGTGGGC | 7088 |
rs754536188 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671973 | TGAGCCAGCCCACTT[A/C]CAAATGGAAAAAGTT | 7088 |
rs754564061 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632041 | GTTGCAGTGAGCCGA[C/G]ATAGTGCTACTGCAC | 7088 |
rs754580128 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643567 | TAGAGACAGGGTCTC[A/C]TTTGGTCACCCAGGT | 7088 |
rs754616158 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660341 | ACAAAGGCTGTTCAC[-/A]AAAAAAAAAAAAACA | 7088 |
rs754628136 | snp | C/T | 1.67733e-05 | 0.00289592 | intron-variant | TLE1 | GRCh38.p7 | 9:81634025 | TGGGGCTCTCTTTAG[C/T]GATGCACACAACTTT | 7088 |
rs754649298 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645011 | GTCTCAAAAAAAAAA[-/AA]AAAAAAAAAAAGGTG | 7088 |
rs754660028 | snp | A/G | 5.84932e-05 | 0.0054077 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687464 | CGAGGGGGACCGAGG[A/G]ACGGGAATGCGGGCG | 7088 |
rs754686474 | snp | A/G/T | 1.65097e-05 | 0.00287308 | missense, synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81654018 | CACAAATCGTATTCA[A/G/T]TCTCTTGGCGATTTC | 7088 |
rs754718815 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645360 | ACAAGAGAGAAACTC[C/T]GTCTCCAAAAAAAAA | 7088 |
rs754748534 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609425 | GGCAGAGTTTTGCTG[C/T]TAAGCAAAACAGACC | 7088 |
rs754783329 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584757 | TGGATACAGGACTAG[C/T]AGCATCATATCCAAC | 7088 |
rs754804824 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639361 | TAAGCTACCATAGCT[A/G]GCCTGCATCTGTACT | 7088 |
rs754822514 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599411 | ACCTACCCCACACAT[C/T]GTGAGCAACATAAGG | 7088 |
rs754839869 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650311 | CAAGAGCTGGGCGGT[A/G]CCTTTGAGAATTTAA | 7088 |
rs754850144 | snp | G/T | 1.64855e-05 | 0.00287097 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81620537 | GCCTCTTAGACTGTC[G/T]GGGACCAGGAGGGAA | 7088 |
rs754866214 | snp | A/T | 1.65067e-05 | 0.00287282 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685796 | ACGTTTGCTAATATC[A/T]TATGAAAAAGGAAAA | 7088 |
rs754868608 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678334 | CCTGCCTCACTCAGC[A/C]CTAGTACTAGCTAGT | 7088 |
rs754880805 | snp | A/G | 2.45137e-05 | 0.00350089 | intron-variant | TLE1 | GRCh38.p7 | 9:81593321 | AAACACATTTACAGA[A/G]GAAGCAATCCCTATC | 7088 |
rs754888298 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659300 | TGCCTTCCACCTCTT[A/G]CAAAGGCTAGACAAC | 7088 |
rs754917414 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647109 | AAGTTCACAGGCATT[-/A]CTATGGGTAACTGCT | 7088 |
rs754927624 | snp | A/G | 3.29522e-05 | 0.00405894 | missense | TLE1 | GRCh38.p7 | 9:81616013 | GATTTCAAAGAAGTG[A/G]AACTTGCCGAGGAGG | 7088 |
rs754936937 | snp | A/G | 1.6972e-05 | 0.00291303 | intron-variant | TLE1 | GRCh38.p7 | 9:81685659 | TCATTTCAGCTTGAA[A/G]TTCAACTAAAGCTTA | 7088 |
rs754953147 | snp | C/G | | | synonymous-codon | TLE1 | GRCh38.p7 | 9:81584511 | ATCTTTTCCAGTACT[C/G]ACAAACCATTTACCT | 7088 |
rs754956435 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653493 | GCTTATACATACATA[C/T]GACTCATTAAGTTAA | 7088 |
rs755017197 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | TLE1 | GRCh38.p7 | 9:81584256 | CCAGTGACTATGTAC[C/T]TATCATCCACAGAGA | 7088 |
rs755058432 | in-del | -/TTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679305 | AAAATTTTTCTTCAC[-/TTTT]TTTTCTTTTTTTTTC | 7088 |
rs755091680 | snp | C/G | 1.66944e-05 | 0.0028891 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81591029 | GGGTAGCAATTTACA[C/G]GAACGGATATAATTG | 7088 |
rs755103802 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656979 | GAGTTTAGGAGGGTT[A/C]CTGCTCTCCCACCCA | 7088 |
rs755131090 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81652228 | CCCCGATGATGGCAT[C/T]CAATTCTGCCATGGT | 7088 |
rs755139526 | snp | G/T | 8.31732e-05 | 0.00644823 | intron-variant | TLE1 | GRCh38.p7 | 9:81593016 | GTGCACCAGTTCCTG[G/T]TCACTCACCAGACAG | 7088 |
rs755143276 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618736 | CTAAAAAGAAAATTA[G/T]GAAAATGGCTAATTT | 7088 |
rs755151637 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686521 | AAAGCCCCTGACAAA[A/G]TAAGAAAATTCACAC | 7088 |
rs755173333 | snp | A/G | 5.59498e-05 | 0.00528883 | intron-variant | TLE1 | GRCh38.p7 | 9:81611991 | GCCGCACATCATTCA[A/G]CTGACCCACTCCATC | 7088 |
rs755203537 | snp | A/G | 3.32878e-05 | 0.00407956 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688289 | CAACTCAATTCTCCG[A/G]TCAATTTCCAACTTT | 7088 |
rs755209010 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673424 | GGAAGGAAGCTGGGT[G/T]TGCAAAAACAAAACG | 7088 |
rs755269357 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612655 | AGCCAAACCGCTGTT[G/T]CAGCCAGTATTAGCA | 7088 |
rs755301693 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626750 | GGTGACACACAGGGC[C/T]GGTTAATGTTGAGGC | 7088 |
rs755308347 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596793 | CAAGGGGCATGGGAG[A/G]GGTTTCTGGGCAATG | 7088 |
rs755322106 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607516 | GTACCTCTAACTCTT[A/G]AAGCTAGCTTTTTCC | 7088 |
rs755325676 | in-del | -/GT | 0.000102073 | 0.00714325 | intron-variant | TLE1 | GRCh38.p7 | 9:81652139 | CACACACACACACAC[-/GT]AAAGCCATCAAATTA | 7088 |
rs755351070 | in-del | -/TGTGTGTGTGT | 3.31909e-05 | 0.00407362 | intron-variant | TLE1 | GRCh38.p7 | 9:81633310 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGT]GTGTGCAGCAGGCGT | 7088 |
rs755354813 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625209 | AATTCTGTGAGAACA[C/G]CAGATCTCAAGAGGG | 7088 |
rs755374213 | snp | C/T | 6.69534e-05 | 0.00578552 | missense, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587712 | TGCTGCTGCAGCTGC[C/T]GCCCCTCGCGCAGGT | 7088 |
rs755377764 | snp | C/G | 5.14558e-05 | 0.00507201 | intron-variant | TLE1 | GRCh38.p7 | 9:81620390 | ATATACTTGGATACT[C/G]AGGTGAGCAGTAAGC | 7088 |
rs755386817 | in-del | GTCACCCAAG/TTTCCC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613944 | ATGGAGTCTCACTCT[GTCACCCAAG/TTTCCC]CTGGAGTGCAGTGGC | 7088 |
rs755437472 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653374 | CAAGGCAAAGCTAAA[A/C]TACAATAGTCTTGAG | 7088 |
rs755455827 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664995 | CCAGGTGCTCTGACA[A/C]CCTCTCTCTAATCTT | 7088 |
rs755457819 | snp | C/T | 0.000200501 | 0.0100105 | intron-variant | TLE1 | GRCh38.p7 | 9:81611755 | CAACCACAGCCCACC[C/T]GACAGCGGCCTACCA | 7088 |
rs755470936 | snp | A/C | 1.65499e-05 | 0.00287657 | intron-variant | TLE1 | GRCh38.p7 | 9:81653937 | CAAACAGAGAAGCAA[A/C]ATAATTGCACTTTAA | 7088 |
rs755482460 | snp | G/T | 1.72647e-05 | 0.00293804 | missense | TLE1 | GRCh38.p7 | 9:81610281 | CTCTCATGTGAGGGG[G/T]AGGATCAAACCCCAC | 7088 |
rs755498685 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663505 | GCTGCAGCAGCACAA[C/G]GACAAGTCCGCATGA | 7088 |
rs755520467 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675950 | GTGATCCGCCCGCCT[C/T]AGCCTCCCAAAGTGC | 7088 |
rs755543044 | in-del | -/CAGGG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591982 | AGGCAGACACCACAC[-/CAGGG]CAGGGCAGGGCAGGG | 7088 |
rs755550817 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637648 | AATGAAAGTTTCTTT[C/T]TTTTTTTTTTTTTTA | 7088 |
rs755553931 | snp | C/T | 6.65602e-05 | 0.00576851 | intron-variant | TLE1 | GRCh38.p7 | 9:81585490 | GGCCTCCAGTTTCCT[C/T]TCGGCTGAACTCACC | 7088 |
rs755577821 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596229 | GATCATCATATGGAG[A/G]CAATTTAAAATTGAT | 7088 |
rs755595344 | snp | A/C | 5.65595e-05 | 0.00531757 | intron-variant | TLE1 | GRCh38.p7 | 9:81600123 | ACAAGGCTCCTAAAC[A/C]GGACAAAGATACAAA | 7088 |
rs755595776 | in-del | -/CAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644004 | TGAAAAGATGTTCAA[-/CAT]CATCAGCCATCAGGA | 7088 |
rs755617941 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631314 | GGAGGTTATCCGACA[C/T]ATTCGGAAATTCAGA | 7088 |
rs755618384 | snp | A/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589113 | TTCCCAGACATCCCC[A/G]CAGAACACCCAGGCC | 7088 |
rs755669409 | in-del | -/CCC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685285 | TGAATACCCTTCTTT[-/CCC]CCCAACAGGTCCACA | 7088 |
rs755687158 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682546 | GTGGGCTAAAATAAG[C/G]TTTATGTGTGCATTT | 7088 |
rs755691614 | snp | A/T | 1.74744e-05 | 0.00295583 | intron-variant | TLE1 | GRCh38.p7 | 9:81600048 | AAGATTCTGAGTTCT[A/T]GGACCTAACTTCCTC | 7088 |
rs755701794 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616030 | ACTTGCCGAGGAGGC[C/T]GTGGAAGCTGGACTG | 7088 |
rs755734666 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625155 | GAAACCATATACTCC[A/G]TAAGAAGGGACTGGA | 7088 |
rs755805745 | snp | A/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586582 | TATATGGTGCATGGC[A/T]GTGCTTATGGATACA | 7088 |
rs755820465 | snp | A/G | 1.65449e-05 | 0.00287614 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634249 | GGGTGAGGCGTAAGG[A/G]GAACTGGGGGTCCGT | 7088 |
rs755830016 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81663208 | CGTCAGGCTCACCAC[G/T]TTTGCGATCAACAGT | 7088 |
rs755874746 | snp | A/C | | | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687781 | GGCGGCGATAATGAC[A/C]CCGGGGACCAGAGGA | 7088 |
rs755914825 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599111 | AAGTAATGAAGCCAC[A/C]TGGGAAAGTACTTCA | 7088 |
rs755927190 | in-del | -/TT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632475 | AATGTTCAGTATCCC[-/TT]TTTTTTTTTTTTTTT | 7088 |
rs755956684 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658277 | CTGAATTCACAGATG[C/T]AGAACCCACAGATAC | 7088 |
rs755961207 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649337 | AAAAATACAACCTCT[C/G]TCTGTCTCCTCGAAG | 7088 |
rs755990174 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632005 | TGAGGCAGAAAAATC[A/G]CTTGAACCCAGGAGG | 7088 |
rs756014556 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647909 | ATATACAACTGTGCC[A/G]TTGTTTACTATTAAT | 7088 |
rs756016452 | in-del | -/A | 4.94849e-05 | 0.00497393 | intron-variant | TLE1 | GRCh38.p7 | 9:81584441 | AGGTGAGGAGTACTT[-/A]ACTCACCTGGAATAT | 7088 |
rs756019706 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670688 | TTGAGCAATTTCAGC[A/G]CTTTGAGAGTTCCAG | 7088 |
rs756035939 | snp | C/T | 3.30109e-05 | 0.00406256 | missense | TLE1 | GRCh38.p7 | 9:81585586 | TGTTCACGTGCAGCA[C/T]CTCCACATTGCTGCT | 7088 |
rs756037729 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671759 | TATCATAGCATCTAG[A/G]GTAGTCGATTATAAA | 7088 |
rs756055341 | in-del | -/TTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661203 | TTATATATATATGTA[-/TTTT]TATATATATATATAT | 7088 |
rs756057481 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618706 | GAAAAAATATAAACT[-/AA]AAGAGTTTCTCTTCT | 7088 |
rs756058663 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622662 | CTTATAATCTGAATA[-/G]GTTTTGAAAAGCTCT | 7088 |
rs756103200 | snp | A/G | 8.35694e-05 | 0.00646357 | intron-variant | TLE1 | GRCh38.p7 | 9:81620608 | CAAGCCTCTTTGTAC[A/G]CATGAAACCCAACCT | 7088 |
rs756105408 | snp | C/G | 1.6641e-05 | 0.00288448 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687292 | GGTGCAAGGGGCACC[C/G]GGACGCCCGCGACCA | 7088 |
rs756150471 | in-del | -/AAAAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625016 | ATATCTGAGAAGTCT[-/AAAAG]AAAAGATCCTCCTAG | 7088 |
rs756171460 | snp | A/G | | | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616068 | CATCCTTCTTTAGCA[A/G]GCGATTTTTGTCGAT | 7088 |
rs756189537 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617222 | CTCTTAAGTAACAAA[A/G]AAGTAAATTAAAAAT | 7088 |
rs756211189 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650735 | AGGCAGTGCCTGGAT[A/C]TGGGGGGAAGAGGAG | 7088 |
rs756229310 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656043 | AGACAAGGTTACAGA[C/T]AGACCATGCCTTGGA | 7088 |
rs756229342 | in-del | -/AGG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634329 | TGGTGAGAGAGAAAA[-/AGG]AGGAGGAGGAGGAGG | 7088 |
rs756240767 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674823 | GGGCAAGTCTAGGAG[G/T]AAAACCCTATAAAAA | 7088 |
rs756256618 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592685 | AATTAAAAAACGAGT[A/G]GATGGCAGGGATCAG | 7088 |
rs756261035 | snp | A/G | 1.66263e-05 | 0.00288321 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81620441 | CCTTTAATTACTTAC[A/G]TAGTGGCTGGAGTCC | 7088 |
rs756300240 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679505 | ACCACACCTCACGGG[C/G]AAAAAAAATCAGAAA | 7088 |
rs756307756 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638185 | ACGCTTAGACTGCAT[C/G]AGTACCATCTCCTGT | 7088 |
rs756317508 | snp | C/T | 1.65384e-05 | 0.00287557 | intron-variant | TLE1 | GRCh38.p7 | 9:81653942 | AGAGAAGCAACATAA[C/T]TGCACTTTAACAGCT | 7088 |
rs756319081 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594436 | CTAACACAGGAACAG[-/A]AAACCAAACCCTGCA | 7088 |
rs756331823 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81652247 | TTCTGCCATGGTCAC[C/T]TGTTTGGCACGTTCA | 7088 |
rs756336432 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628543 | ACAAAGTGATGGATG[A/G]GTGGTCCTAACTAGG | 7088 |
rs756341542 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641269 | GTAAACACGTGCAAA[A/G]GAGCTGTCTGGCAGC | 7088 |
rs756362994 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | TLE1 | GRCh38.p7 | 9:81593180 | GGGTGTTGATCTGGC[A/G]AGCATGCCGGGGGAT | 7088 |
rs756402899 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624019 | TGCTGATTCCCATTA[C/T]AGCCAAAGTGCCTCC | 7088 |
rs756421664 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596055 | TCAGAGAAAGGAGAT[G/T]TTATCTTCCTCCAAC | 7088 |
rs756441320 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605177 | TTGTATAACTTTTAA[C/T]GCCTTGTTCACTCTA | 7088 |
rs756445981 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606398 | ATGATAGACTGGATT[-/A]AAGAAAATGTGGCAC | 7088 |
rs756455023 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615232 | TACTGGGGAGGCTGA[-/G]GCAGGAGAATTGTTT | 7088 |
rs756460400 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632113 | AAAAGACTATCTATA[A/G]GAACCCTGGAATGGC | 7088 |
rs756480525 | snp | A/G | 6.9701e-05 | 0.00590302 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634177 | AGAGCACTAGACAGC[A/G]CAAGAAGGCCGGCAC | 7088 |
rs756497625 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615716 | AGACTCCGTCTCAAA[-/A]AAAAAAAAAAAAAGA | 7088 |
rs756506155 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685396 | GATAAATCTATACAG[A/G]TGAAAAAGTAAACTC | 7088 |
rs756514936 | snp | A/G/T | 0.000114274 | 0.00755811 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611808 | CACGGCGGCCGCGGC[A/G/T]GCTGCGGCGCTCATC | 7088 |
rs756549334 | snp | C/G | 0.000116902 | 0.00764443 | missense, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688219 | AGCCGCGCCTCACCG[C/G]GTGCCGGCTCTGCGG | 7088 |
rs756574404 | snp | C/T | 6.53509e-05 | 0.00571587 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687472 | ACCGAGGGACGGGAA[C/T]GCGGGCGGATGAATA | 7088 |
rs756577937 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634654 | AGTAAGTAAACATGA[C/G]CTAGTTCTGTCTTTA | 7088 |
rs756603542 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633305 | TGTGTGTGTGTGTGT[-/G]TGTGTGTGTGTGTGT | 7088 |
rs756617132 | in-del | -/AAGT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672951 | TCTGCTGTTTGGCCA[-/AAGT]AAGACATTTTACTTA | 7088 |
rs756618408 | snp | C/G | 9.92162e-05 | 0.0070426 | missense, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587726 | CCGCCCCTCGCGCAG[C/G]TCCCAGGACCTGACT | 7088 |
rs756640367 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | TLE1 | GRCh38.p7 | 9:81620505 | GAAAATTCAGGTCCA[C/T]TTCTGCGTTTATCTG | 7088 |
rs756656680 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630082 | GATCCCATCAGTCTC[C/T]GATTTCTGCACTTGG | 7088 |
rs756666224 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685547 | CATCAATCCACAGGA[C/G]AGGAAACCAAGGCAG | 7088 |
rs756724046 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620948 | TCTATTAGACATATT[A/C]TTTAACTGTAAGAGT | 7088 |
rs756729498 | snp | C/T | 6.73809e-05 | 0.00580396 | intron-variant | TLE1 | GRCh38.p7 | 9:81585679 | AGCAAGACAGGCTCA[C/T]TCATTATTCCGCCTG | 7088 |
rs756735716 | in-del | -/TTTTCTTTTTTTTTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613901 | GGAAGACCCCTTTTC[-/TTTTCTTTTTTTTTTT]TTTTCTTTTTTTTTT | 7088 |
rs756747911 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652993 | AGAGATGGAAACTCA[C/G]CCCACACCTCCCAAC | 7088 |
rs756768176 | snp | C/G/T | 8.71735e-05 | 0.00660156 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687301 | GGCACCGGGACGCCC[C/G/T]CGACCACTCGCATGG | 7088 |
rs756776290 | snp | C/T | 3.41279e-05 | 0.00413072 | missense | TLE1 | GRCh38.p7 | 9:81610257 | CCAGGTTTGGAGGAA[C/T]GGTAGGTACTCTCAT | 7088 |
rs756799253 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651841 | AGTAGATTTAGGGAC[A/G]GGCAAGGGGGTGCCT | 7088 |
rs756804367 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611265 | TCCAGAATTCTACCT[C/G]TTTACAGAGACCACT | 7088 |
rs756820131 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609877 | AGCACTGTTGGGAAT[C/T]TCCAGCAGCTGCCCT | 7088 |
rs756827093 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683387 | AGAGAGAATTCCTGT[C/T]AAATCTAATGAGAGC | 7088 |
rs756861362 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623928 | CTCTTCCTCCTCCTG[C/G]TCCTTTAATCTGGAG | 7088 |
rs756865197 | snp | C/T | 1.74848e-05 | 0.0029567 | intron-variant | TLE1 | GRCh38.p7 | 9:81600133 | TAAACAGGACAAAGA[C/T]ACAAATGGAGAAATT | 7088 |
rs756885383 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661760 | ACAACCTTAAATCCC[C/T]CCCCCAAAAAAAATG | 7088 |
rs756928454 | snp | C/G | 1.64961e-05 | 0.00287189 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685836 | TTTGATACCTACCAT[C/G]ACATAGTGCCTCTGC | 7088 |
rs756973589 | in-del | -/TT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662228 | AAACTAAGAGAACAG[-/TT]AAATACGCTACACAC | 7088 |
rs756989666 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685219 | CCCAAAGCATAAAGA[A/G]TACTCCACAGATAGT | 7088 |
rs757023247 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602435 | GGGATGGGACCCAGT[C/T]TAAACACAAAATTCA | 7088 |
rs757042917 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618877 | AAATATAAACCTTCA[C/T]AGGACAGTACATGTC | 7088 |
rs757059974 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626050 | CGAACCCTGAAACCA[-/C]CAGCAGCAAAATGGA | 7088 |
rs757075634 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675614 | GATCACTCTTCCAAA[A/C]GAAAAACTGAGCAAA | 7088 |
rs757093954 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | TLE1 | GRCh38.p7 | 9:81593054 | GGGAGACAGGGCTCT[C/T]ATTGCCAGGGTGGCT | 7088 |
rs757122349 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641253 | AAAACTGGTATGCTA[C/T]GTAAACACGTGCAAA | 7088 |
rs757157020 | in-del | -/G | | | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689656 | GAGCCCGGGAGGTTG[-/G]GGGGTGGGGGGGGGG | 7088 |
rs757164289 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633389 | AGGTTACCAAGAAAC[A/G]CACAGACATGCCCGT | 7088 |
rs757183805 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657231 | CTTTATCAGAGTTTG[C/T]TCAGCTTGCCACTTG | 7088 |
rs757188226 | snp | A/G | 1.64849e-05 | 0.00287092 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81613419 | CTGGAGGCTTGCCGA[A/G]ACCTGGACGGAGGCC | 7088 |
rs757188735 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682444 | AGAAGACAAATCACA[C/T]TGAAAACTGTTCATT | 7088 |
rs757206719 | snp | G/T | 1.88361e-05 | 0.00306883 | intron-variant | TLE1 | GRCh38.p7 | 9:81612001 | ATTCAACTGACCCAC[G/T]CCATCAAACCTGACC | 7088 |
rs757207712 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599725 | AGTTTGGCCATTTGC[A/G]TATTCTTCCAAATAG | 7088 |
rs757231008 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669505 | CTGCAAGCAGTACTG[G/T]AAAGTAGAAATTTTA | 7088 |
rs757250004 | snp | A/G | 2.21702e-05 | 0.00332936 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687393 | GTCCAGGGACTCCGG[A/G]ATAGTGAACTTGAAG | 7088 |
rs757250664 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614490 | CTTTCAACCTTTCAT[A/G]TGCTTTACAACACAG | 7088 |
rs757305908 | snp | A/G | 1.6918e-05 | 0.00290839 | missense | TLE1 | GRCh38.p7 | 9:81611864 | CGTAGGCAGCGCCTG[A/G]GCTGGTCAGCTCGCC | 7088 |
rs757319127 | in-del | -/C | 1.85627e-05 | 0.00304647 | intron-variant | TLE1 | GRCh38.p7 | 9:81611981 | GAAACACAAGCCGCA[-/C]CATCATTCAACTGAC | 7088 |
rs757321525 | in-del | -/TGTGTGTGTGT | 0.000203482 | 0.0100846 | intron-variant | TLE1 | GRCh38.p7 | 9:81633304 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGT]GTGTGTGTGTGCAGC | 7088 |
rs757335878 | snp | C/T | 3.41058e-05 | 0.00412938 | intron-variant | TLE1 | GRCh38.p7 | 9:81590777 | GCTAAAGAAGCGAAC[C/T]CCTCCTTAGACGACC | 7088 |
rs757365643 | snp | A/C | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589377 | TATGACTGTTCAGAA[A/C]GTGCTGGGTTACAGT | 7088 |
rs757385433 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666551 | GGAGGCCGAGGCAGG[C/T]GGATTATGAGGTCAG | 7088 |
rs757388402 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678121 | GTTTTTTATACCTAC[C/T]ATGAGACCTTACAGG | 7088 |
rs757455787 | snp | A/T | 1.71334e-05 | 0.00292684 | intron-variant | TLE1 | GRCh38.p7 | 9:81685632 | TATTATTAAATCATA[A/T]GAACTGATGTCTCAT | 7088 |
rs757480271 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81608218 | CCTCACAACTTTACC[A/G]GTTTGCCCCTTATCC | 7088 |
rs757492038 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638258 | ATCCCTTGCCCCCAG[C/G]TCTCTTCCAAAGAAG | 7088 |
rs757495523 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677335 | CTTTGGGAGGCTGAG[A/G]TGGGCAGATCATGAG | 7088 |
rs757562634 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634597 | TGGTATCACTCACTC[C/T]GAGAGGGGAGCTGTT | 7088 |
rs757565073 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596957 | TCATTTACTTATTCA[A/G]GAGGAAGTCGAGGGG | 7088 |
rs757565583 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594196 | TAAGAGCAAGATGAC[C/T]GGTGCTCCTACGGCC | 7088 |
rs757611928 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644705 | ATGCTTTAAAAAAGA[C/T]GAATTTGGCCAGGTG | 7088 |
rs757622878 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603615 | TTTTCCCCCAATATA[G/T]CTATCTCTTAGTTAC | 7088 |
rs757631994 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673494 | GGGTAGAGTTTTAAA[C/G]GGACTGCTATTTAGA | 7088 |
rs757664691 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590912 | GGCGTAGCAGGCGGG[A/G]GCCGAGGACGTCAGC | 7088 |
rs757739432 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671277 | CCAGCACTTTGGAAG[C/G]CTGAAGCGGGCGGAT | 7088 |
rs757740185 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652136 | ACACACACACACACA[C/T]ACGTAAAGCCATCAA | 7088 |
rs757744984 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643957 | AAGCCATGTGAAGGT[A/G]GATCCACTACAAAAA | 7088 |
rs757764191 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667885 | AAGGATACTCAGACC[C/T]GGGCGTGATGGCTCA | 7088 |
rs757764634 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685495 | TCATTTAAACACTTG[A/T]AATTATCAAGAAGCA | 7088 |
rs757811830 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645367 | GAAACTCCGTCTCCA[-/A]AAAAAAAAAAAATAA | 7088 |
rs757811925 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622627 | CTACTGTAATTTCCG[C/G]TTGAGCGGCTTAAAT | 7088 |
rs757827676 | snp | C/G | 2.36147e-05 | 0.0034361 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688279 | TGTTCCCCGGCAACT[C/G]AATTCTCCGGTCAAT | 7088 |
rs757829888 | snp | A/G | 1.65652e-05 | 0.0028779 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634256 | GCGTAAGGGGAACTG[A/G]GGGTCCGTGGCCATG | 7088 |
rs757839070 | snp | A/G | 1.65173e-05 | 0.00287374 | intron-variant | TLE1 | GRCh38.p7 | 9:81615934 | GTCCTCCAGTCCACA[A/G]TGAAAAATACACTGC | 7088 |
rs757887800 | snp | A/G | 4.94637e-05 | 0.00497287 | intron-variant | TLE1 | GRCh38.p7 | 9:81633403 | CGCACAGACATGCCC[A/G]TTCAGACACAGAGGC | 7088 |
rs757896827 | in-del | -/TTTGTGTGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662360 | TATTAGTGTGCCTGT[-/TTTGTGTGTG]TGTGTGTGTGTGTGT | 7088 |
rs757926502 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626827 | TTGTAGCTGGCCCTT[-/C]TACCCTCCTCCAGGC | 7088 |
rs757939346 | in-del | -/ATT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672325 | CCCCTGCAATAAATT[-/ATT]ATTATTATTATTATT | 7088 |
rs757940369 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584739 | ATCAGCCTCCTTAGT[C/T]ACTGGATACAGGACT | 7088 |
rs758001642 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634415 | ACAGGAGGGGAAGGC[A/G]GAAACAGAACAGGAG | 7088 |
rs758014189 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672268 | ATTAAGAGTAAACAG[A/C]CTAAACTTCCAGTTT | 7088 |
rs758051428 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592628 | TTTTATGCCATGTTA[C/T]CAAATATTTACTATT | 7088 |
rs758054874 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633068 | CAGATCAAAGTGTAT[C/T]TCCAAGTAAGTAATC | 7088 |
rs758090707 | snp | A/G | 1.7146e-05 | 0.00292792 | missense | TLE1 | GRCh38.p7 | 9:81610271 | ATGGTAGGTACTCTC[A/G]TGTGAGGGGGAGGAT | 7088 |
rs758107796 | in-del | -/AAGC | 1.69012e-05 | 0.00290694 | intron-variant | TLE1 | GRCh38.p7 | 9:81652142 | ACACACACACACGTA[-/AAGC]CATCAAATTAATAAG | 7088 |
rs758131644 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603358 | CAGGATATGCCACAC[C/T]AAATATGCCCTTTCG | 7088 |
rs758139879 | snp | A/G | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589945 | ATGGATTTCTACAGC[A/G]GAGGTTTGAAGAGAG | 7088 |
rs758205157 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629842 | GGGGACCACCATCAT[A/G]TATGCAATCCACTGT | 7088 |
rs758213243 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610803 | TATTATCAAATGTCC[G/T]CAAGGGACAAAATCA | 7088 |
rs758220594 | in-del | -/C | | | upstream-variant-2KB, nc-transcript-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81689883 | TGGTGAGGAACTGTT[-/C]CTGGAGGAGCCGCGG | 7088 |
rs758228785 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639388 | TACTCTCTAACCAAA[A/T]CCTGCCCGTCATTTG | 7088 |
rs758246946 | snp | A/C | 1.65108e-05 | 0.00287317 | intron-variant | TLE1 | GRCh38.p7 | 9:81584417 | GACACTGTGGTCAAA[A/C]TGTGGATCTAGGTGA | 7088 |
rs758290503 | snp | C/T | 4.94279e-05 | 0.00497107 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81613453 | AGTGGCGCTGGTGCC[C/T]GGCGTTGGCATGTCG | 7088 |
rs758291312 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651676 | ATGAAATGATAATTC[A/G]GAGACCCATTTTGAC | 7088 |
rs758329199 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609638 | TTCCTGCTTCCCCAC[A/G]AAGCCACTTTGCTTT | 7088 |
rs758334986 | snp | C/G | 1.64732e-05 | 0.0028699 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593190 | CTGGCGAGCATGCCG[C/G]GGGATTCCGGGTCCG | 7088 |
rs758338741 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681299 | TTATGCCTGTAATCC[C/T]AGCACTTTGCGAAGC | 7088 |
rs758342304 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650361 | ATGAAATTATATGTC[A/G]TAATGTAGAGTCTAT | 7088 |
rs758343028 | snp | A/C | 1.64743e-05 | 0.00287 | missense | TLE1 | GRCh38.p7 | 9:81593082 | GCTGATGTCCCAGAC[A/C]TTGACGCAGCCCTTC | 7088 |
rs758349843 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634567 | TATAATCCTCACATC[C/T]ACACTGTCACTTTCT | 7088 |
rs758365931 | in-del | -/T | 1.78998e-05 | 0.00299159 | splice-donor-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587678 | GGAAGCCACTCAGTC[-/T]ACCTGGGAGGTGAAG | 7088 |
rs758385324 | snp | G/T | 2.70977e-05 | 0.00368078 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634129 | TCGTGGTGCTTCTTG[G/T]CATCTTTTATTGCCA | 7088 |
rs758390548 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679689 | TACTTAAAAACCACT[A/G]TACTAAATACCCTGT | 7088 |
rs758455993 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585329 | TTTCTCAAATTAGCA[A/C]AACAGACTGAAACAG | 7088 |
rs758490936 | snp | A/G | 0.000170213 | 0.00922374 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611880 | GCTGGTCAGCTCGCC[A/G]TTCATGCCAGCGTGG | 7088 |
rs758543014 | snp | C/T | 1.64825e-05 | 0.00287071 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590927 | GGCCGAGGACGTCAG[C/T]TCCGCCTTGATGCGC | 7088 |
rs758553876 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607259 | TGAACACAAAGAAAT[G/T]CAAGGTGCTCACAAG | 7088 |
rs758555972 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596311 | GGGAAGCCCATATGG[A/C]TGTTAATACATCAGT | 7088 |
rs758556815 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649150 | TCAATAGTCTCTCCA[G/T]TATCAAATACCTAAG | 7088 |
rs758558917 | snp | C/G | 2.43632e-05 | 0.00349013 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688284 | CCCGGCAACTCAATT[C/G]TCCGGTCAATTTCCA | 7088 |
rs758570134 | snp | A/C | 1.65902e-05 | 0.00288008 | intron-variant | TLE1 | GRCh38.p7 | 9:81611969 | CAGCTGCTGAAAGGA[A/C]ACACAAGCCGCACAT | 7088 |
rs758578413 | snp | A/C | 1.66871e-05 | 0.00288847 | intron-variant | TLE1 | GRCh38.p7 | 9:81620597 | AGATTTCTTCCCAAG[A/C]CTCTTTGTACACATG | 7088 |
rs758596288 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674173 | ATCCATACTGCCATT[-/G]CCCTTGCAAACTGCT | 7088 |
rs758598913 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677262 | AAAAAAAGACCTTAC[-/A]AATTTAAAAGTAAAC | 7088 |
rs758609083 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620252 | GGAAGTCTAAAGCTT[A/C]ACACTGAGCCCGGCA | 7088 |
rs758652385 | snp | A/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686652 | AGGAACAAGGGAAAG[A/T]AACTAACCTTTCTGG | 7088 |
rs758667489 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677560 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 7088 |
rs758695739 | in-del | -/AT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595940 | TGAGAGAAATTACAC[-/AT]GTGAGGATTAGTTTT | 7088 |
rs758736669 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615428 | CCAAGTAAGACGGCA[A/G]TGAGGCTGGGCTTGT | 7088 |
rs758756292 | snp | A/G | 7.02173e-05 | 0.00592484 | intron-variant | TLE1 | GRCh38.p7 | 9:81600157 | AGAAATTCTTGGATG[A/G]AAAGTAAAACAAAAA | 7088 |
rs758789536 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614348 | AACAACACTTTGGAG[G/T]TAAGAGTCACTGCCC | 7088 |
rs758848763 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626961 | GCAAAAACAAAATCT[C/T]TATGTCAAAGCTTTT | 7088 |
rs758867385 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688679 | TTTCTTTGCTCTTCT[C/T]CTGGTCCGCCTCCTC | 7088 |
rs758872059 | snp | A/T | 1.64846e-05 | 0.0028709 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616652 | AATGGTTACCTCATT[A/T]GACACATCCACAACT | 7088 |
rs758886636 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639096 | CCACTACACTTGGCT[-/AA]TTTTTTTTTATAGAG | 7088 |
rs758919266 | snp | C/T | 1.68207e-05 | 0.00290001 | intron-variant | TLE1 | GRCh38.p7 | 9:81616146 | GGTCCTCAACAAGCA[C/T]AATCAAAAGTTTTCG | 7088 |
rs758924851 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603107 | GGGCCTTTGCACATG[C/T]TGCTCTCTCCACCTA | 7088 |
rs758956520 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589272 | AAACACCTTCCTCTG[C/T]TGACATACAGTACCT | 7088 |
rs758956905 | snp | A/C | 1.64852e-05 | 0.00287094 | missense, splice-donor-variant, intron-variant | TLE1 | GRCh38.p7 | 9:81652213 | CTGGTAGGCCACGTA[A/C]CCCGATGATGGCATT | 7088 |
rs758959895 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665218 | TCTGTGGAAAACCTC[A/G]CACAATATTCATTTA | 7088 |
rs759007793 | snp | A/C | 0.0148551 | 0.0848934 | intron-variant | TLE1 | GRCh38.p7 | 9:81652142 | ACACACACACACGTA[A/C]AGCCATCAAATTAAT | 7088 |
rs759016489 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592221 | AAATTAGCCGGGCGT[A/G]GTGGTGGGCGCCCGT | 7088 |
rs759102354 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684584 | GGAAGATCTGAAGGC[A/T]GAACTAATCAATTTC | 7088 |
rs759105396 | snp | A/G | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589700 | TATGAGAACTAAGTG[A/G]AGGAATATTTGAAAA | 7088 |
rs759108177 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593506 | ATTGAACTGTATGTA[A/G]AATTTTTTAAGGGTT | 7088 |
rs759110088 | snp | G/T | 1.64966e-05 | 0.00287194 | missense | TLE1 | GRCh38.p7 | 9:81590955 | CGCGGGGTTGGAGCC[G/T]CCAGGTCCCAAATGG | 7088 |
rs759119505 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678915 | GGAGGCTGAGGAAGG[C/T]GGATCACCTGAGGCT | 7088 |
rs759125514 | snp | C/T | 2.25808e-05 | 0.00336004 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688266 | GCGGCCGGGGCTCTG[C/T]TCCCCGGCAACTCAA | 7088 |
rs759138847 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613170 | AGAAAAGCTGAATGT[A/C]AACAGTTGGAGACTG | 7088 |
rs759146674 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649548 | GTACTCTTTCATGAT[C/T]TTTCACACTTGTAAT | 7088 |
rs759156411 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598111 | GTGAAATTGTTAGCT[A/G]TATTAACAAGGATCA | 7088 |
rs759165064 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655628 | CCATCCTTGACCTTA[C/T]TTATTTCATCATTTT | 7088 |
rs759221468 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655080 | TTTTAAAGAAGGCAG[G/T]AAAGGCCGGGTGCGG | 7088 |
rs759224180 | snp | C/T | 3.30055e-05 | 0.00406222 | missense | TLE1 | GRCh38.p7 | 9:81585577 | TGTCAGGCTTGTTCA[C/T]GTGCAGCACCTCCAC | 7088 |
rs759241232 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627938 | GGAGAGAAAACCAAG[A/G]CTGGGTGCGGTGGCT | 7088 |
rs759245066 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631506 | GCTTCTTTTAGTAAT[C/T]GTGTCACTCACTCCT | 7088 |
rs759281402 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589052 | GATCCAGGTTGAGTC[C/T]TCTCTCCTGCGGCCG | 7088 |
rs759283888 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661419 | CTCAAAACAGGGTGA[A/G]GACTGCTTAAGAGTA | 7088 |
rs759310426 | snp | A/C | 5.59394e-05 | 0.00528834 | intron-variant | TLE1 | GRCh38.p7 | 9:81600114 | GGGGCAGGAACAAGG[A/C]TCCTAAACAGGACAA | 7088 |
rs759310752 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662492 | CCTGAGGTCAGGAGT[A/T]CGAGACCATCCTGGC | 7088 |
rs759316337 | in-del | -/TGTGTGTGTGT | 0.000280387 | 0.011837 | intron-variant | TLE1 | GRCh38.p7 | 9:81633298 | GGGACCGTGTGTGTG[-/TGTGTGTGTGT]GTGTGTGTGTGTGTG | 7088 |
rs759337953 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585261 | TCTCCCAACCCCTCC[A/G]AAACAAACTTGTGTC | 7088 |
rs759352668 | in-del | -/CAGCA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633326 | GTGTGTGTGTGTGTG[-/CAGCA]GGCGTTTGAGTACTT | 7088 |
rs759380504 | snp | A/G | 1.73153e-05 | 0.00294233 | intron-variant | TLE1 | GRCh38.p7 | 9:81616179 | ATTTAGCTTGTAACA[A/G]ACAGACTTTTCCCTT | 7088 |
rs759400561 | snp | C/G | 0.000415189 | 0.0144022 | intron-variant | TLE1 | GRCh38.p7 | 9:81652179 | TGAAAGCTGGTTATA[C/G]ACACTGTAGGAGGTA | 7088 |
rs759451964 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668934 | ATTTATATGCTCCTG[A/T]GTGTTTTTAGAAAAC | 7088 |
rs759500231 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | TLE1 | GRCh38.p7 | 9:81593156 | CGCACACCACCTCCC[C/T]GTGGTTGAGGGTGTT | 7088 |
rs759520610 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658859 | TTCTTAATTTAGCAC[A/C]AATTAACAAGTCTCG | 7088 |
rs759596462 | snp | C/G | 1.64833e-05 | 0.00287078 | missense | TLE1 | GRCh38.p7 | 9:81613503 | TGGATTTCAGAACAG[C/G]CGTGCTGGCTTTTTC | 7088 |
rs759664747 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628917 | TCCCCAGAATTCTGC[-/A]AAAGAGCACGGACCC | 7088 |
rs759670955 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620093 | TATTCAAAAATTGAG[A/G]ACGCAAAGATGGTGA | 7088 |
rs759730592 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595816 | AGAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 7088 |
rs759740647 | snp | A/G | 0.000222551 | 0.0105464 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81613408 | GGGGTCTATGGCTGG[A/G]GGCTTGCCGAGACCT | 7088 |
rs759789297 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600356 | AGTGAGGAATTATTA[C/T]AGCTAAACACAACTG | 7088 |
rs759797315 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687058 | CATGAAGTGCAAATA[-/T]TGACGATTCTCATGC | 7088 |
rs759800377 | snp | C/G/T | 3.3188e-05 | 0.00407346 | intron-variant | TLE1 | GRCh38.p7 | 9:81620575 | GCAAGACAAAAAAAT[C/G/T]AATCAAAGATTTCTT | 7088 |
rs759855576 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682361 | CCAGACTCTGAACAC[A/G]TGCACACAGCTGTAG | 7088 |
rs759860658 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638691 | ATACAGTGGCGCAAT[A/C]TTGGCTCACTACAAT | 7088 |
rs759861676 | snp | C/T | 2.46837e-05 | 0.00351301 | splice-acceptor-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687436 | GCCTGGTGCGGCGTC[C/T]GGGGGCGACCAGCGA | 7088 |
rs759861773 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612854 | CCTGAGGTCAGGAGT[C/T]TGAGACCAGCCTGGC | 7088 |
rs759893062 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648937 | AAGTGAGCTGTGTGT[C/T]AAACCAAATAAACCT | 7088 |
rs759913604 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637997 | CTGTAACCCCAGCAG[C/G]TCAATCATGTTCTCC | 7088 |
rs759971428 | snp | C/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690052 | CGCTAGCGGGAGGGA[C/T]TGGCGAGCGTGCAGC | 7088 |
rs759972395 | in-del | -/G | 1.66029e-05 | 0.00288117 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688271 | GGGGCTCTGTTCCCC[-/G]GGCAACTCAATTCTC | 7088 |
rs759983293 | snp | A/G | 1.65059e-05 | 0.00287275 | intron-variant | TLE1 | GRCh38.p7 | 9:81584399 | ACTCCTGGCTTCAGA[A/G]GCGACACTGTGGTCA | 7088 |
rs759990334 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607967 | AGATATTATAATATA[C/T]GAAAAGTAGAGCAAT | 7088 |
rs759999325 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656412 | GTACATTCCTCTTCT[C/T]GGAAATTCACATTGA | 7088 |
rs760008148 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677704 | AATACCAAACCCAGT[A/C]TCATGGTACATGTAT | 7088 |
rs760020665 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659496 | GAGCTATCCACAAAC[C/T]AAATCTGCATGAAAC | 7088 |
rs760112235 | snp | C/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588899 | CTGTAGAGCTCCAAA[C/G]TTTTAACCTGAGCTT | 7088 |
rs760158012 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681349 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTAGCCA | 7088 |
rs760158779 | in-del | -/GAGCACT | | | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590169 | GAACAGCTCTGGTGT[-/GAGCACT]GACTTCTGAAGGGAG | 7088 |
rs760191046 | snp | G/T | 1.86555e-05 | 0.00305408 | intron-variant | TLE1 | GRCh38.p7 | 9:81634351 | AGGAGGAGGAGGTAG[G/T]GGTGACAGTGATGGC | 7088 |
rs760195159 | snp | A/G | 6.61004e-05 | 0.00574855 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590981 | AATGGACAAAGTACT[A/G]GCTTCCCCTCCCACT | 7088 |
rs760207098 | snp | C/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690033 | TAGAGAGCGCGCGGG[C/G]GCGCGCTAGCGGGAG | 7088 |
rs760228621 | in-del | -/CAGA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597543 | TGGCAAACTGCAGGG[-/CAGA]CAGTCAGTCCTGGAT | 7088 |
rs760245817 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677012 | GAGGCCAAAATGGAC[-/G]GATCACTTGAGGCCA | 7088 |
rs760247851 | snp | A/T | 1.64776e-05 | 0.00287028 | utr-variant-3-prime | TLE1 | GRCh38.p7 | 9:81584189 | TAAACGTTAAACCAC[A/T]TAATGTTTTCAGTAG | 7088 |
rs760271630 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636239 | CACTAATTCTTGCTC[C/T]GTCACCTTTTAAGAG | 7088 |
rs760277091 | snp | A/G | 6.90806e-05 | 0.0058767 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688272 | GGGGCTCTGTTCCCC[A/G]GCAACTCAATTCTCC | 7088 |
rs760293139 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669666 | GGCAGTTCCAAAAAC[G/T]GCGCATTGCTGCTAA | 7088 |
rs760297246 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666076 | GTTTTAGTTCCTAAA[C/T]AGCACATTTCCATTA | 7088 |
rs760300515 | snp | A/C | 1.65018e-05 | 0.00287239 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81652198 | CTGTAGGAGGTAGAC[A/C]TGGTAGGCCACGTAC | 7088 |
rs760346780 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593352 | TCGGCAATGTGCTAC[A/G]ACTATGAAAAAGATG | 7088 |
rs760352158 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677654 | CCTAGACTAGTATCA[C/T]AGACTAGTAACCTAC | 7088 |
rs760377185 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659780 | ACCACTGGGTCCCAA[A/C]CAGGTCTCGTACTTA | 7088 |
rs760401974 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628046 | AACATACTGAGACTC[-/T]TGACTGTACAAAAAT | 7088 |
rs760403527 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676904 | TGTTCATTTATTTTA[A/G]ATGTATACAACAGTG | 7088 |
rs760417005 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596736 | CAGGCAAAATTCATC[C/T]GCAGTATTGAAAGTC | 7088 |
rs760457380 | snp | C/T | 2.10799e-05 | 0.00324646 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587640 | AAGACACACCCCAGC[C/T]ACCTCCCAGACTCCA | 7088 |
rs760491481 | snp | A/G | 3.29674e-05 | 0.00405988 | intron-variant | TLE1 | GRCh38.p7 | 9:81616724 | AGAAACATTAACGCC[A/G]TTTACTAAAAGCTAA | 7088 |
rs760495202 | in-del | -/CCCA | 4.54122e-05 | 0.00476488 | intron-variant | TLE1 | GRCh38.p7 | 9:81611749 | CTACCCCAACCACAG[-/CCCA]CCCGACAGCGGCCTA | 7088 |
rs760561709 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684537 | AATTCAACTCTGAAA[C/T]ACACTTGCTTAATGA | 7088 |
rs760564543 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602977 | GAGGGAAGGTGACCA[C/G]GGTGGTTGGGAAACC | 7088 |
rs760568080 | snp | A/G | 1.72439e-05 | 0.00293627 | missense | TLE1 | GRCh38.p7 | 9:81610233 | ACGGTTTCCCCCCAG[A/G]GATTCCTGCCAGGTT | 7088 |
rs760585209 | snp | C/T | 2.35446e-05 | 0.003431 | missense, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687371 | ACTGGAATTCCTCTT[C/T]AATCCGGTCCAGGGA | 7088 |
rs760605215 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643426 | TTTTTAGTAGAGATG[C/G]GGTTTCTCCATGTTA | 7088 |
rs760665325 | snp | C/T | 3.32519e-05 | 0.00407736 | intron-variant | TLE1 | GRCh38.p7 | 9:81584553 | AGGAATATCTAGTTT[C/T]CACAAGGTTAAAATT | 7088 |
rs760673552 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644770 | AGGCAGAGACAGGTG[A/G]ATCACCTGAGGTCAG | 7088 |
rs760689687 | in-del | -/A | 3.31639e-05 | 0.00407196 | intron-variant | TLE1 | GRCh38.p7 | 9:81620567 | ATTACTCTGCAAGAC[-/A]AAAAAATTAATCAAA | 7088 |
rs760700744 | in-del | -/CGTCC | 4.45981e-05 | 0.00472197 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687295 | CAAGGGGCACCGGGA[-/CGTCC]CGCCCGCGACCACTC | 7088 |
rs760702874 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600173 | AAAGTAAAACAAAAA[C/G]AGGCTTAATATATTG | 7088 |
rs760719049 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646848 | TTAATTTTATACTAA[C/G]TTGTTTTAAAATATA | 7088 |
rs760760153 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599317 | GGAGCTGTTAATCTT[C/T]ACCTTAGCTTCCACA | 7088 |
rs760761168 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602021 | AAAGTGTGAGAAGTG[G/T]CATAAGATGTTTCAC | 7088 |
rs760805742 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630873 | TTTTATGTAACTGTA[C/G]CAAAATCCCACTAAT | 7088 |
rs760806106 | snp | C/G | 5.81514e-05 | 0.00539187 | intron-variant | TLE1 | GRCh38.p7 | 9:81600081 | TCAATTACACGTTTC[C/G]AAACTTCTCAATGTG | 7088 |
rs760806413 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643080 | TGCGGGGTAGGGGAA[A/C]ATGAGGAGCAATTGG | 7088 |
rs760830963 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640903 | TAAGCTCCTTACCAC[C/G]AACCATGGAATCAAC | 7088 |
rs760850752 | snp | A/G | 3.90419e-05 | 0.00441808 | intron-variant | TLE1 | GRCh38.p7 | 9:81593288 | CACTTTTGGAAAAAC[A/G]ATTGGAGAGAAGACA | 7088 |
rs760880218 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652741 | AGCCCAGGAGTTCAA[A/G]ACCAGCATGGGCAAC | 7088 |
rs760908788 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681155 | GAGATGTTGCTTGCT[A/G]AAATATCACATGGAG | 7088 |
rs760917982 | snp | A/G | 1.81506e-05 | 0.00301247 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611952 | CAGGGGTGTCCTCAA[A/G]CCAGCTGCTGAAAGG | 7088 |
rs760939085 | snp | A/T | 6.60535e-05 | 0.00574651 | intron-variant | TLE1 | GRCh38.p7 | 9:81615947 | CAATGAAAAATACAC[A/T]GCCAAACAGGCAAGT | 7088 |
rs760958215 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610653 | GGCCAAACAGTTCTT[G/T]TCTTTGTTAGGGGCC | 7088 |
rs761015345 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655023 | GCCCAGGGGTCAGCT[A/G]AACATAATAAAAGGT | 7088 |
rs761054671 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606972 | CTCATGCCTGTAGTC[C/T]CAGCACTTTGGGAGG | 7088 |
rs761074510 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647402 | TTGCACATCAAAAGC[C/T]AAATGGCCATCCTTT | 7088 |
rs761086976 | snp | C/T | 2.38024e-05 | 0.00344973 | intron-variant | TLE1 | GRCh38.p7 | 9:81620933 | AAATCTTGAGATTAC[C/T]CTATTAGACATATTC | 7088 |
rs761089702 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678969 | AACATGCAGAAACCC[C/T]ATCTCTACCAAAAAA | 7088 |
rs761107451 | snp | A/G | 1.66045e-05 | 0.00288132 | intron-variant | TLE1 | GRCh38.p7 | 9:81620580 | ACAAAAAAATTAATC[A/G]AAGATTTCTTCCCAA | 7088 |
rs761126083 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657630 | TAAAGAAAAGAAAGA[C/G]ATATGAAAGCAAAGG | 7088 |
rs761133237 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591844 | ATGCACTAATAACTA[C/T]TCTAAAAAAAGTCTG | 7088 |
rs761145427 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618181 | TGGAAAAAGCAGGAC[A/C]TCTCAATGGTTTTGA | 7088 |
rs761158986 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687147 | CAATGGGAGGAGGAG[A/G]AGACAAGAGAAGAGG | 7088 |
rs761159557 | in-del | -/CCCACAC | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686976 | CTTTGCTTCCCTGAA[-/CCCACAC]CCCACACTCCAGGAC | 7088 |
rs761180829 | in-del | -/CG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621971 | AATATAGAGAAGCTC[-/CG]TAAGTAATGTCTTTA | 7088 |
rs761193291 | snp | C/T | 3.32546e-05 | 0.00407752 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685767 | TTAACTCATGTTTTT[C/T]ACACTCTGCTAACAC | 7088 |
rs761196109 | snp | C/T | 3.29973e-05 | 0.00406172 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585551 | GCTCTCATGCAGGTG[C/T]AGCTGGTACTTGTCA | 7088 |
rs761223347 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595867 | ACAATTGAGTTGCAC[A/G]TGATTTAAAGGATGG | 7088 |
rs761247928 | in-del | -/GGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662387 | GTGTGTGTGTGTGTG[-/GGTG]TGTGTGTGTGTGTGT | 7088 |
rs761261619 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636919 | GAGGCAGGAGAATCA[A/T]TTGAACCCGAGTGGC | 7088 |
rs761276934 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596707 | AAATGACCGCATTTC[C/T]AGAATTTCGAACACA | 7088 |
rs761304901 | snp | A/C/G | 3.29969e-05 | 0.00406172 | intron-variant | TLE1 | GRCh38.p7 | 9:81616632 | AGACAAACTTTGATG[A/C/G]AAAGAATGGTTACCT | 7088 |
rs761318865 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647166 | CTCTGAGGCCACAAA[C/T]AGAAACCTGGCATTT | 7088 |
rs761323211 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | TLE1 | GRCh38.p7 | 9:81584217 | TAGATGACTTCATAG[A/G]CTGTAGCCTTCTTGT | 7088 |
rs761328398 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595918 | CTTCTCAAAGATCTC[A/G]GTGCCATGAGAGAAA | 7088 |
rs761355337 | snp | C/T | 5.7282e-05 | 0.00535142 | intron-variant | TLE1 | GRCh38.p7 | 9:81611726 | GCTCAATGGAGCATG[C/T]AGCGTTCCTACCCCA | 7088 |
rs761367476 | in-del | -/A | 0.48 | 0.0979796 | intron-variant | TLE1 | GRCh38.p7 | 9:81616151 | TCAACAAGCATAATC[-/A]AAAGTTTTCGTGATT | 7088 |
rs761398565 | in-del | -/TG | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588828 | TGGGAATTTCAACAC[-/TG]AGAAGAAAGTTACCA | 7088 |
rs761445388 | snp | C/T | 1.64841e-05 | 0.00287085 | intron-variant | TLE1 | GRCh38.p7 | 9:81616730 | ATTAACGCCATTTAC[C/T]AAAAGCTAAGAATAG | 7088 |
rs761493251 | snp | A/C/G | 4.96457e-05 | 0.00498205 | intron-variant | TLE1 | GRCh38.p7 | 9:81652302 | TGCTTTGAAAACAAG[A/C/G]AGAAGAAAGGGCATT | 7088 |
rs761513817 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687028 | GTTTCAGCTCAGTCT[A/G]CTGAAAAATAAATAC | 7088 |
rs761514885 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613906 | ACCCCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 7088 |
rs761522386 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604923 | TTTACATGTCTCCCT[A/G]TCACCCACTGCTCTG | 7088 |
rs761568746 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686233 | TACTCCACCAAAATC[C/T]GGCCCTTGCACAATC | 7088 |
rs761572604 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683534 | AAGAATTATGATTAC[C/T]AGCTGCACCAAATGC | 7088 |
rs761580625 | snp | A/T | 2.72194e-05 | 0.00368903 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634114 | CTGTGGTGCTCTGCA[A/T]CGTGGTGCTTCTTGT | 7088 |
rs761583328 | snp | C/T | 3.29902e-05 | 0.00406128 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81652202 | AGGAGGTAGACCTGG[C/T]AGGCCACGTACCCCG | 7088 |
rs761587408 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676044 | TTAATCTGAATTCCA[C/T]GGACTTGTTGAAGGA | 7088 |
rs761595127 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665887 | TTTTAAAGAATTCAG[C/T]TGCATTTTCCAAGAT | 7088 |
rs761601256 | snp | C/T | 2.75243e-05 | 0.00370964 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687449 | TCTGGGGGCGACCAG[C/T]GAGGGGGACCGAGGG | 7088 |
rs761610320 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587798 | AGAAATGTCAATACA[A/G]CTGGCTCCGTCTGTG | 7088 |
rs761615259 | snp | C/T | 2.22299e-05 | 0.00333383 | missense | TLE1 | GRCh38.p7 | 9:81611789 | GGGAGCGCCCGTAGG[C/T]CACCACGGCGGCCGC | 7088 |
rs761618615 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642226 | AGAACTACTTTCTCA[A/G]AAAGGTTAATTATCC | 7088 |
rs761652322 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588541 | GACTCTGCCTCCAAG[C/T]GGAGCACAAGGTTGT | 7088 |
rs761679442 | snp | C/T | 1.65072e-05 | 0.00287286 | missense | TLE1 | GRCh38.p7 | 9:81613520 | GTGCTGGCTTTTTCA[C/T]GCTGGTGTCATTAAA | 7088 |
rs761697046 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689337 | AGAGTAGTCACAGCG[A/G]TGGGGCCAGCGGGGG | 7088 |
rs761713981 | snp | A/G | 3.29511e-05 | 0.00405887 | missense | TLE1 | GRCh38.p7 | 9:81613473 | TTGGCATGTCGCTCC[A/G]AGGCGTTGGTGTGCT | 7088 |
rs761737424 | snp | A/C | 1.90199e-05 | 0.00308376 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688177 | GAGAAGCGCCTCCCC[A/C]ACGATCCTGGCCCCC | 7088 |
rs761745608 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653665 | CTTTCTATTTAAAAG[A/G]TATAAAAGACACCTG | 7088 |
rs761752099 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610565 | GGTAAATACTTCCCT[C/T]AGACTTGCAAGCAAG | 7088 |
rs761857555 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583977 | ACCCATGGCCCCTCT[C/G]TCCGCTTGGCCTTGG | 7088 |
rs761859545 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604232 | CCCCATCCTAGGCTG[A/T]GAGCTCCCGGTGGGG | 7088 |
rs761884149 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623424 | CAAATCGAGGCAACA[G/T]TTATGAGGACACCAT | 7088 |
rs761905154 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598282 | AAAATATCACATGCT[A/G]TCACATCTCCAAGTT | 7088 |
rs761945692 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586219 | AGACGGGGTTTCACC[A/G]TGCCAGCCAGGATGG | 7088 |
rs761955140 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639985 | CAAGCAGAACCAATT[C/T]TGACACCCCTCCCCT | 7088 |
rs761983600 | snp | A/G | 1.66189e-05 | 0.00288256 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585650 | GCAGTACCCCAGGGA[A/G]AAGATCTACAAGGAG | 7088 |
rs761998220 | snp | A/T | 3.29973e-05 | 0.00406172 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585566 | CAGCTGGTACTTGTC[A/T]GGCTTGTTCACGTGC | 7088 |
rs762008562 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651483 | AGAGCAGAACCCCGG[A/T]GAAAAGCCAGGGAGC | 7088 |
rs762009314 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679132 | CAGTCTGGGTAACAG[A/T]TTAAGACTCTATCGC | 7088 |
rs762037662 | in-del | -/CAACTTTGCAGCACTGTAAGAGTATGAGGACAAAGTCCTAATCTGGCTTG | 9.00779e-05 | 0.0067105 | intron-variant | TLE1 | GRCh38.p7 | 9:81634034 | CTTTAGCGATGCACA[lengthTooLong]CCCGGCCTCTCACCT | 7088 |
rs762062247 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613232 | AACATCTGTTTCTTA[C/T]CATGGCTTTTTCAGA | 7088 |
rs762063797 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650122 | CCTGCCTTTATAATA[A/C]CCTCCACAACATTTT | 7088 |
rs762080253 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622448 | AATGTCTTGTTTTTT[G/T]TTGTTGTTGTCGTTT | 7088 |
rs762087759 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616991 | CAAATACTTGGCAGA[C/T]TGTAAGAGCTCAGTA | 7088 |
rs762088247 | snp | G/T | 3.48268e-05 | 0.00417279 | intron-variant | TLE1 | GRCh38.p7 | 9:81600112 | CTGGGGCAGGAACAA[G/T]GCTCCTAAACAGGAC | 7088 |
rs762090758 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585236 | TCTTCAGAGTAGAAA[C/G]TCATTGTCGTCTCCC | 7088 |
rs762129634 | in-del | -/CCATA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658395 | GAAAAACATCGAAAG[-/CCATA]CCATACCATATGTCC | 7088 |
rs762176197 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594926 | CTCCATAAAAGCAAA[A/G]TATCAGACACATGAA | 7088 |
rs762202352 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591689 | ATGCTTTTAACGATG[G/T]ATTATCTTTCAAAGA | 7088 |
rs762203483 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669861 | TTTGCTGGTTTGGCC[A/G]AGCGACTTTTTAAAG | 7088 |
rs762221881 | snp | C/T | 1.65263e-05 | 0.00287452 | splice-donor-variant, intron-variant | TLE1 | GRCh38.p7 | 9:81613376 | AGAGGCGATGCTGTA[C/T]CCGCTTGGTTAACGA | 7088 |
rs762230554 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680971 | AGGTAAAATTTGCAA[A/G]AGAGTAAAAGAATCA | 7088 |
rs762237796 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646221 | TGATGACAATAATCC[A/G]GACACTGAGGAAAAG | 7088 |
rs762240122 | snp | A/T | 0.00138815 | 0.0263087 | intron-variant | TLE1 | GRCh38.p7 | 9:81633339 | TGCAGCAGGCGTTTG[A/T]GTACTTACTGTGCCC | 7088 |
rs762240300 | snp | C/G | 1.83562e-05 | 0.00302948 | intron-variant | TLE1 | GRCh38.p7 | 9:81611966 | AGCCAGCTGCTGAAA[C/G]GAAACACAAGCCGCA | 7088 |
rs762247113 | in-del | -/AC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662233 | AGAGAACAGTTAAAT[-/AC]ACGCTACACACCAAC | 7088 |
rs762256837 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669083 | GTTCCCACAGGGCTG[C/G]GTTGGCTCAATAATG | 7088 |
rs762267468 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599243 | TAGGCTAAGTAACTC[A/G]CCCATAACCACGGCT | 7088 |
rs762273790 | in-del | -/CGTGTGTGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633288 | TTGTCAGAAGGGGAC[-/CGTGTGTGTG]TGTGTGTGTGTGTGT | 7088 |
rs762285695 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629398 | ATTTCTCTGCTCAAG[A/C]GCTGCACTTATATAA | 7088 |
rs762297110 | snp | A/G | 1.65721e-05 | 0.0028785 | missense | TLE1 | GRCh38.p7 | 9:81591001 | CCCCTCCCACTATGA[A/G]AGTGCAGCCATCGGG | 7088 |
rs762324915 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595300 | TATGGGATACTTGGA[G/T]TCATAATCAAATAGC | 7088 |
rs762328282 | snp | C/G/T | 4.94746e-05 | 0.00497346 | intron-variant | TLE1 | GRCh38.p7 | 9:81620947 | CTCTATTAGACATAT[C/G/T]CTTTAACTGTAAGAG | 7088 |
rs762349898 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640804 | GCACATGGCTTATCA[A/C]CATGTTGTTGTAGCC | 7088 |
rs762363918 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616821 | ACCTGGGACAGGCCT[A/G]CAGGCTCTCTATCAG | 7088 |
rs762400678 | snp | C/T | 0.000214276 | 0.0103485 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590933 | GGACGTCAGCTCCGC[C/T]TTGATGCGCGGGGTT | 7088 |
rs762409898 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604798 | CTCAAGCTCTCTCTC[C/T]GTGCACGACACAGAC | 7088 |
rs762424164 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595694 | TATGGTGGCGGGCGC[C/T]TGTAGTCCCAGCTAC | 7088 |
rs762447392 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656414 | ACATTCCTCTTCTCG[A/G]AAATTCACATTGAAG | 7088 |
rs762462947 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617974 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCATTGC | 7088 |
rs762503461 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642901 | TACCATTCAGCCTTG[-/A]AAAAGAAGAAAATCC | 7088 |
rs762519138 | snp | C/T | 1.72931e-05 | 0.00294045 | missense | TLE1 | GRCh38.p7 | 9:81611832 | GCTCATCTGGGGCGA[C/T]ATGTTGTGTAAACTG | 7088 |
rs762526090 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654410 | CAGTGGCACGATCTC[A/G]GCTCACCACAAGCTC | 7088 |
rs762531169 | snp | C/T | 3.30513e-05 | 0.00406504 | missense, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81654030 | TCAATCTCTTGGCGA[C/T]TTCAGTCTATAAAGA | 7088 |
rs762531727 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592720 | CAGGCCCAGTTGTGC[-/T]TTTGTCCATTAAATG | 7088 |
rs762604016 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612075 | AGAGAAAGAGGTAAG[C/G]CTTCTAGGGGAGGGG | 7088 |
rs762606911 | snp | C/T | 2.23028e-05 | 0.00333929 | missense | TLE1 | GRCh38.p7 | 9:81611798 | CGTAGGCCACCACGG[C/T]GGCCGCGGCGGCTGC | 7088 |
rs762620954 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600629 | AGCATTTAATAGACC[-/AA]AAAAAAAAAAAAAAA | 7088 |
rs762624916 | snp | C/G | 1.64874e-05 | 0.00287113 | missense | TLE1 | GRCh38.p7 | 9:81620480 | CACCTTCCTTTTCTT[C/G]ATGTCATTGGAAAAT | 7088 |
rs762658437 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616811 | TAAAAAAACTACCTG[A/G]GACAGGCCTGCAGGC | 7088 |
rs762663570 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624851 | TAGGAGTAATACAGC[C/T]CACGGAGGACATTAC | 7088 |
rs762672919 | in-del | -/GCCAGG | 1.79194e-05 | 0.00299322 | splice-acceptor-variant | TLE1 | GRCh38.p7 | 9:81593276 | GAAGGAGTATGCACT[-/GCCAGG]TTTGGAAAAACGATT | 7088 |
rs762704806 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637003 | GGGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGA | 7088 |
rs762717135 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | TLE1 | GRCh38.p7 | 9:81616741 | TTACTAAAAGCTAAG[A/G]ATAGGTTTGAGGCAC | 7088 |
rs762739239 | snp | A/C | 1.65157e-05 | 0.0028736 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634213 | CCGAGGGGCGGGATT[A/C]CAGGAGGCTGAAGTC | 7088 |
rs762753346 | snp | C/T | 1.6483e-05 | 0.00287076 | missense | TLE1 | GRCh38.p7 | 9:81590848 | ACACAGCGATGTTGC[C/T]GTCGCTGCAGCATGA | 7088 |
rs762757169 | in-del | -/GA | | | downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583241 | AAAAAAAAAAAAAAG[-/GA]GAGAGAGAGAGAGAG | 7088 |
rs762768481 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643259 | GTTTTTTTTTTTGAC[A/T]GAGTTTCGCTCTCGT | 7088 |
rs762776946 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664584 | AAATGTGGGGAGGTC[A/G]GGCACAGTGGCTCAC | 7088 |
rs762804281 | in-del | -/ATC | 1.6507e-05 | 0.00287284 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685793 | AACACGTTTGCTAAT[-/ATC]ATATGAAAAAGGAAA | 7088 |
rs762820434 | snp | A/G | 2.0461e-05 | 0.00319845 | intron-variant | TLE1 | GRCh38.p7 | 9:81593297 | AAAAACGATTGGAGA[A/G]AAGACAGAAAACACA | 7088 |
rs762829886 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662960 | TTAAGCGATTCTCAT[G/T]CCTCAGCCTCCCGAG | 7088 |
rs762906318 | snp | A/C | 1.91053e-05 | 0.00309068 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688190 | CCAACGATCCTGGCC[A/C]CCCACCACCACCCAG | 7088 |
rs762908072 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639591 | TTTTTTTTTTTTGTT[G/T]TTTTTTTTTTTGAGA | 7088 |
rs762939877 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649862 | AATTTTCCAGAACGC[A/G]CACAATTCCTTTCAG | 7088 |
rs762957415 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583786 | ATTTCACAAGATGCA[A/G]AACCAGGAAACAAGT | 7088 |
rs762991990 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627549 | ACTTTCTCAAAGAAG[A/C]ACCATTTTTTTAAGC | 7088 |
rs762992718 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595861 | AGTAAAACAATTGAG[C/T]TGCACATGATTTAAA | 7088 |
rs762997653 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600509 | TCACCTCAACTTAAT[C/T]TCAAAAAATTAAGCT | 7088 |
rs763090334 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688708 | TCTTCGGGCTTTCCC[A/C]GAGGCGGCGGCGGGC | 7088 |
rs763113408 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659622 | TCCAAATTACCTGTC[-/T]TACAACAGTCTTTCA | 7088 |
rs763116993 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624758 | TTTCTAGACTGTATG[-/T]TAAGTTTTCATTTAA | 7088 |
rs763128272 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592333 | ACTGCACTCCAGCCT[A/G]GGCGACAGAGCAAGA | 7088 |
rs763175102 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659686 | TTGCATATGGTAATA[C/T]AGTTAGCCCTCATCA | 7088 |
rs763182346 | snp | A/C/G | 5.02991e-05 | 0.00501472 | intron-variant | TLE1 | GRCh38.p7 | 9:81585669 | ATCTACAAGGAGCAA[A/C/G]ACAGGCTCACTCATT | 7088 |
rs763209645 | snp | C/T | 2.7772e-05 | 0.00372629 | missense, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687347 | ACCTGTGATACTGCG[C/T]CTGCAGGAACTGGAA | 7088 |
rs763209889 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660977 | ACACACACACACACA[-/C]CATTTAGCCTGGCGT | 7088 |
rs763218739 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673064 | GATTACTTGAGGTCA[A/G]GAGTTTGTGACCAGC | 7088 |
rs763222115 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669022 | CCACAGCACCAGAAA[A/C]CAAATTTAACCCACG | 7088 |
rs763227241 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659049 | GAGTAGCTGGGATGA[C/T]AGGCACGCGCCACCA | 7088 |
rs763239835 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684302 | CTGAGAAACACACAA[A/G]AACAAAGGCACAAAC | 7088 |
rs763258493 | in-del | -/AAAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628616 | TAGAGAAGAGTAACA[-/AAAG]AAAGAAACCACTTTA | 7088 |
rs763272010 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671535 | CTGTAATCCCAGCTA[C/T]TCGAGAGGCCAAGGC | 7088 |
rs763278604 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602639 | AGCATTTTGGATTTT[C/G]AATTTTCGAATTAAG | 7088 |
rs763285619 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629088 | GTGACATAAAATGGA[A/T]CACTGCAAAATGATA | 7088 |
rs763296482 | snp | C/T | 1.6855e-05 | 0.00290297 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685936 | AATGTAAACATTATG[C/T]CACTTGTTTTAACAT | 7088 |
rs763305957 | snp | A/G | 1.65181e-05 | 0.00287381 | intron-variant | TLE1 | GRCh38.p7 | 9:81584348 | TTAATGTGGAACAAC[A/G]GTACTCAGAGGCCCT | 7088 |
rs763314890 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639053 | TCAGGCTCCTAAGTA[C/G]ATACTTAGCTGGGAC | 7088 |
rs763324365 | snp | A/C | 1.64727e-05 | 0.00286986 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593139 | GTTGCTGATGGTCAC[A/C]GCGCACACCACCTCC | 7088 |
rs763355063 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680645 | TCAGTCCTGCTTGCT[A/G]ATAAGAAACAAAGGC | 7088 |
rs763394241 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672992 | AAGACTGCCAACAAG[G/T]CCGGACGCGGTGGCT | 7088 |
rs763405167 | in-del | -/AAAAAAAAAAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645001 | GTGAGACACTGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAGGTG | 7088 |
rs763410698 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639877 | CAGGCATGAACCACC[A/G]CGCCCAGCTGAGAAA | 7088 |
rs763411738 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679034 | ACGCCTGTAATCCCA[C/G]CTATTCCAGAGGCTG | 7088 |
rs763413555 | snp | C/T | 1.68539e-05 | 0.00290287 | intron-variant | TLE1 | GRCh38.p7 | 9:81592993 | ATCTCCAGGGAGAAA[C/T]TGCCCTTGTGCACCA | 7088 |
rs763466369 | snp | C/T | 1.65116e-05 | 0.00287324 | intron-variant | TLE1 | GRCh38.p7 | 9:81616612 | CATTATTCAAATCAT[C/T]CTGAAGACAAACTTT | 7088 |
rs763479608 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666976 | AATTTAAAAATTAGC[C/T]GGGTGTGGTGGTGTG | 7088 |
rs763521609 | in-del | -/CTTTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632475 | AAATGTTCAGTATCC[-/CTTTTT]TTTTTTTTTTTTTTT | 7088 |
rs763526143 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661576 | GGCAAACTGATCTTC[C/T]GGTTTCTTTGAACCA | 7088 |
rs763593631 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597575 | ATCCCTCCTTAGGGG[A/C]CATACAGCGAAGCCC | 7088 |
rs763615307 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604825 | AGACTGTGCCTCCCC[A/G]GTTCCATGGGAAACT | 7088 |
rs763622791 | snp | C/T | 1.64993e-05 | 0.00287218 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81652199 | TGTAGGAGGTAGACC[C/T]GGTAGGCCACGTACC | 7088 |
rs763627029 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585358 | AGACATTGCTGTGCT[C/G]TGAAGGGCATATTAA | 7088 |
rs763678422 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595479 | CAAAAACAACAAAAA[A/T]ATTGCCAGGTGATAC | 7088 |
rs763687845 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644657 | CGTGATGGTTGTACA[G/T]CAATGTGAATACGCT | 7088 |
rs763696519 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685187 | AGCCACTAATCCTGA[A/C]TATTGCTTCATGCAG | 7088 |
rs763758142 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637644 | CTACAATGAAAGTTT[-/C]TTTTTTTTTTTTTTT | 7088 |
rs763767382 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81635581 | GTAAAAATGATTAAG[A/G]CTCAATTTCTAAGGT | 7088 |
rs763774150 | snp | A/G | 0.000149042 | 0.00863128 | missense | TLE1 | GRCh38.p7 | 9:81616121 | GCAGGGCTTGCTCGC[A/G]GAGAAGAAGGGTCCT | 7088 |
rs763827797 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643380 | TAGCTGGGGTTACAG[C/G]CATGTGCCACCACGC | 7088 |
rs763838771 | snp | C/T | 0.00641163 | 0.0562557 | missense | TLE1 | GRCh38.p7 | 9:81590986 | ACAAAGTACTGGCTT[C/T]CCCTCCCACTATGAG | 7088 |
rs763838904 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656424 | TCTCGGAAATTCACA[C/T]TGAAGGTTTCCAGTT | 7088 |
rs763887999 | snp | A/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588512 | CTGAGGCAGACCCAC[A/G]GGCACCTCAGCAAGA | 7088 |
rs763914038 | snp | A/G | 4.13052e-05 | 0.00454433 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587649 | CCCAGCCACCTCCCA[A/G]ACTCCAGGGCAGGCG | 7088 |
rs763921600 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686712 | AAAATTTATAAGTCC[C/T]TTGAAGGTAAGTCTC | 7088 |
rs763933279 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682368 | CTGAACACGTGCACA[C/T]AGCTGTAGGCAGAGC | 7088 |
rs763936153 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653595 | AAAGAACTATCTGCC[C/T]CCATAGTAAAGTCTA | 7088 |
rs764003346 | snp | A/G | 4.50177e-05 | 0.00474413 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687293 | GTGCAAGGGGCACCG[A/G]GACGCCCGCGACCAC | 7088 |
rs764004060 | snp | C/T | 1.68117e-05 | 0.00289923 | intron-variant | TLE1 | GRCh38.p7 | 9:81585675 | AAGGAGCAAGACAGG[C/T]TCACTCATTATTCCG | 7088 |
rs764004507 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641133 | TTGACAGTTCTCTCC[A/T]AATCACTCTTCCTTG | 7088 |
rs764007714 | snp | G/T | 5.78486e-05 | 0.00537782 | intron-variant | TLE1 | GRCh38.p7 | 9:81611719 | TGACAGCGCTCAATG[G/T]AGCATGCAGCGTTCC | 7088 |
rs764071768 | snp | A/G | 2.28684e-05 | 0.00338137 | missense, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687377 | ATTCCTCTTTAATCC[A/G]GTCCAGGGACTCCGG | 7088 |
rs764086428 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624927 | AAATTCTAAAACCAA[A/G]TAATTTTCTACACCT | 7088 |
rs764104183 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606788 | AATTAAAAAAAAAAC[-/C]ATATATATATATATA | 7088 |
rs764122993 | snp | A/T | 1.65072e-05 | 0.00287286 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685786 | CTCTGCTAACACGTT[A/T]GCTAATATCATATGA | 7088 |
rs764143771 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623816 | AAAATGAAAAATAAA[A/C]ATCAAAAAAATAAAA | 7088 |
rs764167489 | snp | A/G | 8.23608e-05 | 0.00641667 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593157 | GCACACCACCTCCCC[A/G]TGGTTGAGGGTGTTG | 7088 |
rs764182891 | in-del | -/GAGTCTCCTCCA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628985 | ACACCGTCTGCTCTG[-/GAGTCTCCTCCA]GAGTCTCCTCCCTTT | 7088 |
rs764187323 | snp | A/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690280 | GTGAGGCCACATTCA[A/G]AAATTTATCTGAGGT | 7088 |
rs764208025 | snp | A/C | 1.65053e-05 | 0.0028727 | intron-variant | TLE1 | GRCh38.p7 | 9:81584414 | GGCGACACTGTGGTC[A/C]AACTGTGGATCTAGG | 7088 |
rs764226533 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681875 | TTCATCAGCACAAAG[A/T]GTCAGAACTGAAGAG | 7088 |
rs764228375 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609274 | ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCACATT | 7088 |
rs764242457 | in-del | -/TCCATCCC/TCCC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584968 | GCACTCATCCACCCA[-/TCCATCCC/TCCC]TCCATCCATCCATCC | 7088 |
rs764273154 | snp | C/T | 3.32712e-05 | 0.00407854 | intron-variant | TLE1 | GRCh38.p7 | 9:81584554 | GGAATATCTAGTTTT[C/T]ACAAGGTTAAAATTC | 7088 |
rs764302356 | in-del | -/CAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616269 | CAAGGTGACCAACAC[-/CAT]GTTATAAATGAGCAA | 7088 |
rs764344585 | in-del | -/T | 0.000526607 | 0.0162181 | intron-variant | TLE1 | GRCh38.p7 | 9:81633302 | CCGTGTGTGTGTGTG[-/T]GTGTGTGTGTGTGTG | 7088 |
rs764384098 | in-del | -/CCCTCTGGG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594210 | TGGTGCTCCTACGGC[-/CCCTCTGGG]CCCTCTGGGCCACAA | 7088 |
rs764391791 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620256 | GTCTAAAGCTTAACA[A/C]TGAGCCCGGCAGAAG | 7088 |
rs764408333 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629142 | CAGTACTCGGGCACA[C/T]AGTCAGGGCTCAACA | 7088 |
rs764412759 | snp | A/G | 0.000115362 | 0.00759393 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590900 | GCTGATGGCCAGGGC[A/G]TAGCAGGCGGGGGCC | 7088 |
rs764415586 | snp | C/T | 3.29462e-05 | 0.00405857 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593187 | GATCTGGCGAGCATG[C/T]CGGGGGATTCCGGGT | 7088 |
rs764417473 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | TLE1 | GRCh38.p7 | 9:81615969 | CAGGCAAGTGTCAGT[C/T]TTCTTTACCTACCAA | 7088 |
rs764434188 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659083 | CTGGCTAATTTTTCT[A/G]TTTTTAGTAGAGATG | 7088 |
rs764459748 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639879 | GGCATGAACCACCGC[A/G]CCCAGCTGAGAAAAA | 7088 |
rs764480923 | in-del | -/TGTGTGTGTGTGTGTGTCATCCCGCC | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587910 | TAGTTTTGGACCGTG[-/TGTGTGTGTGTGTGTGTCATCCCGCC]TGTGTGTGTGTGTGT | 7088 |
rs764505495 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609031 | AAAGAAAAAGAAAAA[A/C]AACAACATTTGCAAA | 7088 |
rs764541554 | snp | C/T | 1.64982e-05 | 0.00287208 | missense | TLE1 | GRCh38.p7 | 9:81585555 | TCATGCAGGTGCAGC[C/T]GGTACTTGTCAGGCT | 7088 |
rs764569524 | snp | C/T | 1.81701e-05 | 0.00301409 | missense | TLE1 | GRCh38.p7 | 9:81611954 | GGGGTGTCCTCAAGC[C/T]AGCTGCTGAAAGGAA | 7088 |
rs764577076 | snp | C/G | 1.95173e-05 | 0.00312383 | missense, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688220 | GCCGCGCCTCACCGG[C/G]TGCCGGCTCTGCGGG | 7088 |
rs764599170 | snp | G/T | 1.66145e-05 | 0.00288218 | intron-variant | TLE1 | GRCh38.p7 | 9:81620583 | AAAAAATTAATCAAA[G/T]ATTTCTTCCCAAGCC | 7088 |
rs764602742 | snp | C/T | 5.60271e-05 | 0.00529249 | intron-variant | TLE1 | GRCh38.p7 | 9:81611729 | CAATGGAGCATGCAG[C/T]GTTCCTACCCCAACC | 7088 |
rs764627595 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679052 | ATTCCAGAGGCTGAG[A/G]CAGGAGAATCACCTG | 7088 |
rs764811077 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684628 | AGCCGGTCAGCCATG[C/T]TCTTTAATTTAATGA | 7088 |
rs764832905 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593634 | TATCTTGTGTAATTG[C/T]ATGATTTCTTAGTAT | 7088 |
rs764848082 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603126 | TCTCTCCACCTAGAG[C/G]TTCAGCCCCTTCCCC | 7088 |
rs764897862 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644593 | AAATGGTAATGAATA[C/T]GGAGTTTCTTTACAG | 7088 |
rs764939737 | snp | A/T | 1.70688e-05 | 0.00292132 | missense | TLE1 | GRCh38.p7 | 9:81610260 | GGTTTGGAGGAATGG[A/T]AGGTACTCTCATGTG | 7088 |
rs764949398 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655644 | TTATTTCATCATTTT[C/G]TCAATGCTTACTAAA | 7088 |
rs764951106 | snp | A/G | 6.59348e-05 | 0.00574135 | intron-variant | TLE1 | GRCh38.p7 | 9:81616731 | TTAACGCCATTTACT[A/G]AAAGCTAAGAATAGG | 7088 |
rs764952576 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662566 | AGCAGGGCATGGTGA[C/T]GCATGCCTGTAATCC | 7088 |
rs764953567 | in-del | -/TA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668386 | AAAGATTATTTTAAG[-/TA]TATTTAGAAGAGAGT | 7088 |
rs764965189 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661797 | GAAACCTCACCGGCA[A/G]CCAAACAAAAATGTA | 7088 |
rs764973198 | in-del | -/CAAG | 1.6489e-05 | 0.00287128 | intron-variant | TLE1 | GRCh38.p7 | 9:81633380 | TGCTCCCGAGGTTAC[-/CAAG]CAAGAAACGCACAGA | 7088 |
rs764973698 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | TLE1 | GRCh38.p7 | 9:81584220 | ATGACTTCATAGACT[A/G]TAGCCTTCTTGTCCC | 7088 |
rs764974988 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667303 | CAGAAGGCTGAGGTA[A/C]AAGAATCGCTTAAAC | 7088 |
rs764975355 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667387 | AGACAGACTGTCTCA[-/A]AAAAAAAAAAAAAAA | 7088 |
rs764989923 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674475 | CTGGTCCTTACCCCC[-/G]TTACCACCCAAGGTC | 7088 |
rs765000370 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655093 | AGGAAAGGCCGGGTG[C/T]GGTGGCTCGCGCCTG | 7088 |
rs765020307 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651647 | AGCAAAAGGCAAAAA[G/T]CAAGGATAACTAAAT | 7088 |
rs765033736 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622572 | TGGACCTTTAAGACT[C/G]TCAAGCTTTGAGGCC | 7088 |
rs765062037 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686328 | TATCTGTTAAGTTAC[C/T]CCTACAATTGCTGGT | 7088 |
rs765073998 | snp | G/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691472 | TTCTCATTAAGTACA[G/T]TTGGGAAGGCGGCTG | 7088 |
rs765077861 | snp | C/T | 1.65397e-05 | 0.00287569 | intron-variant | TLE1 | GRCh38.p7 | 9:81613526 | GCTTTTTCATGCTGG[C/T]GTCATTAAACAAATT | 7088 |
rs765086994 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634369 | TGACAGTGATGGCGA[C/T]GGAGGCGGCATCCAG | 7088 |
rs765089691 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629182 | CAAATGACTCAAAGT[-/A]TTTAAAAGCATGCCC | 7088 |
rs765146278 | snp | A/G | 1.64868e-05 | 0.00287109 | intron-variant | TLE1 | GRCh38.p7 | 9:81633395 | CCAAGAAACGCACAG[A/G]CATGCCCGTTCAGAC | 7088 |
rs765146342 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601844 | AAAGAATGAATCACA[-/G]GATCTTACACAATCC | 7088 |
rs765152012 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661398 | CATAATGAGTGCTGT[C/T]TGAAGCTCAAAACAG | 7088 |
rs765164451 | snp | A/G | 1.87587e-05 | 0.00306252 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587666 | CTCCAGGGCAGGCGG[A/G]AGCCACTCAGTCACC | 7088 |
rs765201214 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674264 | GCTTGCCTTCTAATG[A/C]AGTTTTCTATTGTGT | 7088 |
rs765206911 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595279 | ACAGGAACCTATGCC[A/G]CTTATTATGGGATAC | 7088 |
rs765210129 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587804 | GTCAATACAGCTGGC[C/T]CCGTCTGTGTGGCCC | 7088 |
rs765221739 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669431 | ACCTTCTAAGCCACA[C/G]ACTAATGCTTATTCA | 7088 |
rs765235238 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628932 | AAAAGAGCACGGACC[A/C]ACCCAGTCCATCCAT | 7088 |
rs765260417 | snp | A/G | 1.69801e-05 | 0.00291372 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611873 | CGCCTGGGCTGGTCA[A/G]CTCGCCGTTCATGCC | 7088 |
rs765262347 | snp | A/G | 0.00012563 | 0.00792459 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687438 | CTGGTGCGGCGTCTG[A/G]GGGCGACCAGCGAGG | 7088 |
rs765277119 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620099 | AAAATTGAGAACGCA[A/G]AGATGGTGAGATCAG | 7088 |
rs765322991 | in-del | -/TATATGG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631600 | CCATAATGCCTTACA[-/TATATGG]TATGCACTCAATGAA | 7088 |
rs765348578 | snp | A/C/G | 0.000200795 | 0.010018 | intron-variant | TLE1 | GRCh38.p7 | 9:81620593 | TCAAAGATTTCTTCC[A/C/G]AAGCCTCTTTGTACA | 7088 |
rs765381200 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591903 | TTGGAAACACCTTCT[C/G]TGGAATCCTTACAAT | 7088 |
rs765384100 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598456 | ATAGTACTTCTCATA[C/T]GGTGAACATTTAAGT | 7088 |
rs765385372 | snp | C/G/T | 0.000448768 | 0.0149733 | intron-variant | TLE1 | GRCh38.p7 | 9:81600113 | TGGGGCAGGAACAAG[C/G/T]CTCCTAAACAGGACA | 7088 |
rs765390633 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607166 | TGAGAAAAGTACCCC[A/G]ACATAGTATCACAAC | 7088 |
rs765431763 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622407 | CTGCGCATCCAAGCC[A/C]CAGGGCCATTCCAAG | 7088 |
rs765437865 | snp | A/C/T | 3.30111e-05 | 0.00406259 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685794 | ACACGTTTGCTAATA[A/C/T]CATATGAAAAAGGAA | 7088 |
rs765452266 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642081 | TGAAATGGTGGGTAA[A/C]AAAAAGACAAAGATA | 7088 |
rs765465569 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666355 | TAAACCTCTTCACAT[A/G]TCTTAGTCATTAGAG | 7088 |
rs765466583 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620400 | ATACTCAGGTGAGCA[C/G]TAAGCAAACAAATAT | 7088 |
rs765473779 | snp | A/T | 1.68046e-05 | 0.00289862 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685933 | CTTAATGTAAACATT[A/T]TGTCACTTGTTTTAA | 7088 |
rs765474657 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638016 | ATCATGTTCTCCAGA[A/G]TAAGAAAGGAAAAGG | 7088 |
rs765486796 | snp | C/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589154 | CCTGCTTCACTTGGT[C/G]AAAGTGTTGCTTTCC | 7088 |
rs765498274 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631053 | TATTCATTGAAATGA[C/T]TAGAACTTGTCAAAA | 7088 |
rs765546549 | snp | C/T | 3.29979e-05 | 0.00406175 | missense | TLE1 | GRCh38.p7 | 9:81585570 | TGGTACTTGTCAGGC[C/T]TGTTCACGTGCAGCA | 7088 |
rs765547223 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611341 | ATAGAAAGAGAAAGC[A/G]ATGGCTTCTCAGACA | 7088 |
rs765579714 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664984 | TTAGCACCTGCCAGG[-/T]TGCTCTGACACCCTC | 7088 |
rs765597716 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670360 | AGACAGAGTCTGGGT[C/T]TGTCGCCCAGGCTGG | 7088 |
rs765641074 | snp | C/G | 1.71108e-05 | 0.00292491 | intron-variant | TLE1 | GRCh38.p7 | 9:81592976 | AGCTATTTCCTTATT[C/G]AATCTCCAGGGAGAA | 7088 |
rs765660055 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81652209 | AGACCTGGTAGGCCA[C/T]GTACCCCGATGATGG | 7088 |
rs765705505 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596814 | CTGGGCAATGATCCT[A/G]CTCTGTTCCTTGATC | 7088 |
rs765708347 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638013 | TCAATCATGTTCTCC[A/G]GAATAAGAAAGGAAA | 7088 |
rs765729050 | snp | A/C | 1.66056e-05 | 0.00288141 | missense | TLE1 | GRCh38.p7 | 9:81591009 | ACTATGAGAGTGCAG[A/C]CATCGGGTAGCAATT | 7088 |
rs765747123 | snp | A/G | 3.67417e-05 | 0.00428597 | intron-variant | TLE1 | GRCh38.p7 | 9:81611967 | GCCAGCTGCTGAAAG[A/G]AAACACAAGCCGCAC | 7088 |
rs765754457 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680914 | TGAGAAACTGTAGAC[-/AA]AAACACACAGGGTTA | 7088 |
rs765768882 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656491 | ATGCACACAGATACA[C/T]ATACAGAAATATAAA | 7088 |
rs765770161 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607988 | GTAGAGCAATGGGAA[A/T]CGGCTTTCCTAAAAA | 7088 |
rs765782977 | in-del | -/TTTTCTTTTTTTTTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613902 | GGAAGACCCCTTTTC[-/TTTTCTTTTTTTTTTT]TTTTTTTTGAGATGG | 7088 |
rs765797713 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615003 | AGTTCAAGACCAGCA[A/T]GGCCAACATGAAACC | 7088 |
rs765804625 | snp | C/G | 1.91963e-05 | 0.00309802 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688196 | ATCCTGGCCCCCCAC[C/G]ACCACCCAGCCGCGC | 7088 |
rs765806788 | snp | G/T | 2.80753e-05 | 0.00374658 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634141 | TTGTCATCTTTTATT[G/T]CCAAGTGAGACTGCC | 7088 |
rs765826858 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683724 | CTATGAAGAACATGG[C/T]GTCTCTCAGCTTTTC | 7088 |
rs765859071 | snp | C/T | 1.65927e-05 | 0.00288029 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587838 | AATTGCCTGATAAAA[C/T]AAACCAGATTGAATA | 7088 |
rs765877046 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667956 | ATTGCCTGAGGCCAA[C/G]AGTTCGAGATCAGCC | 7088 |
rs765914853 | snp | C/T | 1.66352e-05 | 0.00288398 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688282 | TCCCCGGCAACTCAA[C/T]TCTCCGGTCAATTTC | 7088 |
rs765925365 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655047 | AAAAGGTGTCCTTAG[C/T]GTCTATAGCACGGGC | 7088 |
rs765941638 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669713 | CCAAGTGTCCAATTA[A/C]AGCTGCTTAATCATT | 7088 |
rs765955468 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613810 | TGGACTTTGGGTCTA[C/T]GCCAAGTTAGAAAGA | 7088 |
rs765988528 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632473 | TTAAATGTTCAGTAT[-/C]CCTTTTTTTTTTTTT | 7088 |
rs765995052 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636377 | GTGCTTGGAGAAGGA[A/T]GAGGAACAGGACTGC | 7088 |
rs766023964 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637875 | GTAGGTATCATGATA[C/T]CTACCCATTTCACAG | 7088 |
rs766027430 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653961 | ACTTTAACAGCTGAA[C/T]AATTTTACTTACTTC | 7088 |
rs766051918 | snp | A/G | 5.13448e-05 | 0.00506653 | synonymous-codon, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587696 | CTGGGAGGTGAAGTC[A/G]TGCTGCTGCAGCTGC | 7088 |
rs766087125 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610368 | ACATCAATACTGTTC[A/G]TTAGAAACTCACAGA | 7088 |
rs766098929 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677671 | GACTAGTAACCTACT[C/T]AGATCAGTCATGGTG | 7088 |
rs766136702 | snp | A/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690034 | AGAGAGCGCGCGGGC[A/G]CGCGCTAGCGGGAGG | 7088 |
rs766138801 | snp | C/T | 4.94572e-05 | 0.00497254 | missense | TLE1 | GRCh38.p7 | 9:81620482 | CCTTCCTTTTCTTGA[C/T]GTCATTGGAAAATTC | 7088 |
rs766140837 | snp | C/T | 5.20522e-05 | 0.00510131 | intron-variant | TLE1 | GRCh38.p7 | 9:81611737 | CATGCAGCGTTCCTA[C/T]CCCAACCACAGCCCA | 7088 |
rs766150162 | snp | A/G | 0.000232408 | 0.0107773 | intron-variant | TLE1 | GRCh38.p7 | 9:81593303 | GATTGGAGAGAAGAC[A/G]GAAAACACATTTACA | 7088 |
rs766168019 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81584095 | GGTTTGGAAACAGGT[A/G]TTTGTAATTTTTTTT | 7088 |
rs766181933 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601166 | GTCCACTAAATAAGC[A/G]AGCTGTGGAATCTAG | 7088 |
rs766188469 | in-del | -/CATA/CATCAATA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584970 | ACTCATCCACCCATC[-/CATA/CATCAATA]CATCCATCCATCCAT | 7088 |
rs766215524 | in-del | -/A | 3.31639e-05 | 0.00407196 | intron-variant | TLE1 | GRCh38.p7 | 9:81620566 | ATTACTCTGCAAGAC[-/A]AAAAAAATTAATCAA | 7088 |
rs766255854 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643456 | AGTCAGGCTGGTCTG[C/G]AACTCCCAACCTCAG | 7088 |
rs766286430 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625243 | CTTCACTGGCAACAA[A/G]CAAATTGCTATTTAT | 7088 |
rs766303559 | in-del | -/C | 3.29029e-05 | 0.0040559 | intron-variant | TLE1 | GRCh38.p7 | 9:81611764 | CCCACCCGACAGCGG[-/C]CTACCATGGGGGAGC | 7088 |
rs766307778 | snp | A/G | 4.94336e-05 | 0.00497135 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81615997 | CAAGCTCATTTCTTT[A/G]GATTTCAAAGAAGTG | 7088 |
rs766314117 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644378 | TTGATGAAATGTTAA[C/T]TGTCAATAAAAAGGA | 7088 |
rs766324350 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673166 | TAATCCCAGCTACTC[C/G]GGAGGCTGAGGCAAC | 7088 |
rs766361312 | snp | C/T | 4.53566e-05 | 0.00476196 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634230 | AGGAGGCTGAAGTCC[C/T]GAAGGGTGAGGCGTA | 7088 |
rs766396917 | in-del | -/AGAAAACCCAATTTT | 2.34535e-05 | 0.00342436 | cds-indel, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687422 | GGGCTGGCCTGCAGC[-/AGAAAACCCAATTTT]CTGGTGCGGCGTCTG | 7088 |
rs766421499 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674944 | AGGATCACTTGAGTC[C/T]AGGAATTCGAGACCA | 7088 |
rs766426943 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680694 | TCTAGGCTCTAAATG[C/G]AGAGAGCTTTCTCTC | 7088 |
rs766428558 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670233 | ATATTAACCAGTATG[C/T]GACAAACAGTAGAAT | 7088 |
rs766430333 | snp | A/G | 3.2987e-05 | 0.00406108 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81613390 | ACCCGCTTGGTTAAC[A/G]AGGGGGTCTATGGCT | 7088 |
rs766449020 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591850 | TAATAACTACTCTAA[A/C]AAAAGTCTGTGTTTC | 7088 |
rs766476839 | snp | A/G | 1.84759e-05 | 0.00303935 | intron-variant | TLE1 | GRCh38.p7 | 9:81611975 | CTGAAAGGAAACACA[A/G]GCCGCACATCATTCA | 7088 |
rs766483409 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640976 | ACTATGTCATAAAAA[C/T]CACAGACTTAACCCA | 7088 |
rs766523794 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599386 | ACGTGGGACCCACCA[A/G]GACAAAGACACCTAC | 7088 |
rs766540282 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652776 | CAGAACCCTGTCTCT[A/G]TTTTTAAAATAAATA | 7088 |
rs766585636 | in-del | -/GTGGTTTATGC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681279 | CATCGGCCGGGCACA[-/GTGGTTTATGC]CTGTAATCCCAGCAC | 7088 |
rs766629482 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630906 | GGACAGTGAACAGTT[C/T]AATTCCTCTCTATGG | 7088 |
rs766640361 | in-del | -/TGAGCAC | | | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590167 | AGAACAGCTCTGGTG[-/TGAGCAC]TGAGCACTGACTTCT | 7088 |
rs766650627 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596768 | AGGTGGTGGTTAACC[C/T]TGGTGACTGCAAGGG | 7088 |
rs766655166 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640119 | TCCTACAATGCACAG[A/G]ACAGCCCTCACCACA | 7088 |
rs766684644 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629708 | GCTCCTAGGCTACAA[A/G]CCTGTACATGTTACT | 7088 |
rs766766065 | snp | C/T | 2.67019e-05 | 0.0036538 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687351 | GTGATACTGCGCCTG[C/T]AGGAACTGGAATTCC | 7088 |
rs766809076 | snp | C/T | 1.64887e-05 | 0.00287125 | intron-variant | TLE1 | GRCh38.p7 | 9:81616747 | AAAGCTAAGAATAGG[C/T]TTGAGGCACAGTTAG | 7088 |
rs766816814 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596112 | ATGTTCCAGATTAAA[C/T]AGATGCACCGAGTAA | 7088 |
rs766841635 | in-del | -/TCCCTTTTTTTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632471 | TTTAAATGTTCAGTA[-/TCCCTTTTTTTTT]TCCCTTTTTTTTTTT | 7088 |
rs766860747 | snp | C/T | 0.000164742 | 0.00907435 | missense | TLE1 | GRCh38.p7 | 9:81584232 | ACTGTAGCCTTCTTG[C/T]CCCCCGAGCCAGTGA | 7088 |
rs766868731 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664766 | ATGGTTAGTGAGGTT[A/G]TCAGTGGTTCTCAAA | 7088 |
rs766873870 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605297 | GCAGTGAGATGAGTG[C/T]AGTCATCGAGAGTGA | 7088 |
rs766879401 | snp | C/T | 1.68258e-05 | 0.00290045 | intron-variant | TLE1 | GRCh38.p7 | 9:81592998 | CAGGGAGAAATTGCC[C/T]TTGTGCACCAGTTCC | 7088 |
rs766885541 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655079 | GTTTTAAAGAAGGCA[A/G]GAAAGGCCGGGTGCG | 7088 |
rs766890696 | in-del | -/AGG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634330 | TGGTGAGAGAGAAAA[-/AGG]AGGAGGAGGAGGAGG | 7088 |
rs766927458 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657667 | ATACAGTGGTCTCTC[A/G]GTATCTGTGAGGGAT | 7088 |
rs766928015 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596198 | TCCTCTTCTTTAAAC[C/T]GCACAGGAGGCCTGC | 7088 |
rs766938374 | in-del | -/G | | | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689662 | GGGAGGTTGGGGGGT[-/G]GGGGGGGGGCAGAAG | 7088 |
rs766956470 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609941 | TCTGAGGGGTCAGGC[A/G]AAGAGGGCCAGCCAC | 7088 |
rs766958038 | snp | C/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686430 | AAGTTCTCCCTGCTG[C/G]GTAAACACGGTGTGT | 7088 |
rs766958776 | in-del | -/TTTTTTTTTTTTTTTTTTTTTAAGACAAAGTCTCGCTCTGTCACCTA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657905 | CACTACAGACATAAT[lengthTooLong]TTTTTTTTTTTTTTT | 7088 |
rs766960608 | in-del | -/TTACTGATAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672889 | AACACAACTTTATTC[-/TTACTGATAG]TTACATTACTTAAAG | 7088 |
rs766974014 | snp | A/G | 4.94482e-05 | 0.00497209 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81652217 | TAGGCCACGTACCCC[A/G]ATGATGGCATTCAAT | 7088 |
rs766996780 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653028 | AACTCCACCCACAAA[C/T]AAAAACAAAGCCATA | 7088 |
rs767010305 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618227 | GAGGTCCTGAATTTA[C/T]GATCTAAACAATTCT | 7088 |
rs767061744 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597152 | ATAGGAATAATAATA[A/G]AACACAGAGGTCGCA | 7088 |
rs767078673 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586452 | CAACTGTAGCATAAC[A/G]GGAAGTATTTGTACA | 7088 |
rs767121039 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612469 | TGGGCCCAGGTTGTT[A/G]CTTTTTTCCTTTCCC | 7088 |
rs767128786 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654814 | TGACCTCTTTGCCAC[C/T]TGTCCCAGCTCTTGT | 7088 |
rs767130693 | snp | C/T | 4.80158e-05 | 0.00489955 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634242 | TCCCGAAGGGTGAGG[C/T]GTAAGGGGAACTGGG | 7088 |
rs767150131 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636925 | GGAGAATCATTTGAA[C/T]CCGAGTGGCAGAGGT | 7088 |
rs767177968 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625123 | CTTGAGATGATTAGA[G/T]GAGGTGCAAGAACAC | 7088 |
rs767214653 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585448 | CCATATTTTTTTAAG[-/A]AAGCATTTTCCATTT | 7088 |
rs767260624 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633464 | ATTAGAACACAAGCC[C/T]CAAACAGTTTTAAAA | 7088 |
rs767262164 | snp | C/G | 1.64789e-05 | 0.0028704 | missense | TLE1 | GRCh38.p7 | 9:81590883 | CAGACCTTGGAATCG[C/G]GGCTGATGGCCAGGG | 7088 |
rs767266631 | snp | C/T | 3.85989e-05 | 0.00439294 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688207 | CCACCACCACCCAGC[C/T]GCGCCTCACCGGGTG | 7088 |
rs767307172 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646393 | AATTTAAGTAGAGAG[G/T]ACGTCACTAAATACA | 7088 |
rs767319041 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675540 | TTTTTTAGTCCAAAC[C/T]CAAACATATTACTAC | 7088 |
rs767344041 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592352 | GACAGAGCAAGACTC[C/T]GTCTCAAAGAAAAAA | 7088 |
rs767353825 | snp | A/G | 9.14495e-05 | 0.00676139 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687285 | CCGGCTGGGTGCAAG[A/G]GGCACCGGGACGCCC | 7088 |
rs767369905 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643272 | ACAGAGTTTCGCTCT[C/T]GTTGCCCAGGCTGGA | 7088 |
rs767371485 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645062 | CATATCTCAATTTTA[A/T]AAATAACACACAATA | 7088 |
rs767387640 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653735 | AAGCTGTACATTGGA[G/T]AGTCATTTTGCAGTT | 7088 |
rs767395378 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601972 | GGAAGCAGATAGAAA[C/T]ACGGCTTGTACACGA | 7088 |
rs767397418 | snp | A/G | 1.65026e-05 | 0.00287246 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585578 | GTCAGGCTTGTTCAC[A/G]TGCAGCACCTCCACA | 7088 |
rs767424843 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642292 | TTCTGGATTTTTTTC[A/C]GATTTTTAAATATTT | 7088 |
rs767483304 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683601 | AGGATGTTTTTCAAA[C/T]GTAAGTCCACTTTAA | 7088 |
rs767523340 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613669 | TGTTGACAGCATTAA[C/T]TTGTGAGCGAGAAAT | 7088 |
rs767533883 | in-del | -/C | 3.49852e-05 | 0.00418227 | frameshift-variant | TLE1 | GRCh38.p7 | 9:81610224 | AGGTACTTACGGTTT[-/C]CCCCCCAGGGATTCC | 7088 |
rs767574757 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626445 | CAACTGGTCATTCAC[A/G]TACTCTGCCTAACAC | 7088 |
rs767590678 | in-del | -/TGTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633303 | GTGTGTGTGTGTGTG[-/TGTT]TGTGTGTGTGTGTGT | 7088 |
rs767626559 | snp | A/G | 3.30366e-05 | 0.00406413 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593034 | ACTCACCAGACAGTC[A/G]AGCTGGGAGACAGGG | 7088 |
rs767635585 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610591 | GCAAGTTCACAGAGC[A/C]GTATGTTGTATTAGG | 7088 |
rs767678023 | snp | C/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690404 | GCGTAGGTACACCAG[C/G]AAAGACGACTGTGAT | 7088 |
rs767688613 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609335 | GGTGATCCACCCGCC[A/T]CAGCCTCCCAAAGTG | 7088 |
rs767692012 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585240 | CAGAGTAGAAACTCA[C/T]TGTCGTCTCCCAACC | 7088 |
rs767701106 | in-del | -/GG | | | upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689655 | TGAGCCCGGGAGGTT[-/GG]GGGGTGGGGGGGGGG | 7088 |
rs767747399 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656309 | GTCTATTTGAGTGCA[-/T]GTAAAGGAGTAGAGA | 7088 |
rs767786728 | in-del | -/TGG | 0.000469947 | 0.0153216 | intron-variant | TLE1 | GRCh38.p7 | 9:81634305 | AACTGCTGCTGCTGT[-/TGG]TGGTGGTGGTGGTGA | 7088 |
rs767810637 | in-del | -/AC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607341 | ACCCTGTTAATACAC[-/AC]ACACACACACACACA | 7088 |
rs767812841 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618118 | CTTCTTAGCCAAAAC[A/G]TCTCATGTCCTTTAG | 7088 |
rs767831637 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646270 | CCTAGTTGTGCTCTC[A/T]GTAAAAACAAACAAA | 7088 |
rs767832933 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651510 | GAGCACTAGGGCAGA[C/T]AATTAACAATTCTTC | 7088 |
rs767850932 | snp | C/T | 4.94531e-05 | 0.00497234 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81613504 | GGATTTCAGAACAGG[C/T]GTGCTGGCTTTTTCA | 7088 |
rs767854001 | snp | C/T | 1.65872e-05 | 0.00287981 | intron-variant | TLE1 | GRCh38.p7 | 9:81584545 | ATTAGCAAAGGAATA[C/T]CTAGTTTTCACAAGG | 7088 |
rs767869635 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639034 | CTCAAGCAATCCTCT[C/G]ACCTCAGGCTCCTAA | 7088 |
rs767882808 | snp | A/C | 1.64822e-05 | 0.00287068 | missense | TLE1 | GRCh38.p7 | 9:81620491 | TCTTGATGTCATTGG[A/C]AAATTCAGGTCCATT | 7088 |
rs767885851 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650211 | CTATTTTTATTCTCT[A/G]ATTCAGCTCAAAATG | 7088 |
rs767910088 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604355 | GTGGGAACCCTAAAC[A/C]ATGGCCCACAAGAGA | 7088 |
rs767996349 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685513 | TTATCAAGAAGCAAC[C/T]CTTGATGCAGAATAC | 7088 |
rs767997181 | in-del | -/GGA | 1.84001e-05 | 0.0030331 | intron-variant | TLE1 | GRCh38.p7 | 9:81593279 | GGAGTATGCACTTTT[-/GGA]GGAAAAACGATTGGA | 7088 |
rs768009353 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654595 | ATCCGCCCGCCTCGG[C/T]CTCCCAAAGTGCTGG | 7088 |
rs768019399 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617035 | GCTGAATTTCTCGAG[C/G]GATGAAATCTTTAAT | 7088 |
rs768027243 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605887 | CCATCTGACAAAGGG[-/C]TAATATCCAGAATCT | 7088 |
rs768040777 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669181 | AGGGAATAAAGGTCA[A/G]TGTTGCACTTTTGGT | 7088 |
rs768069156 | snp | A/G | 1.65836e-05 | 0.0028795 | intron-variant | TLE1 | GRCh38.p7 | 9:81654058 | AGACAAAGCCACACA[A/G]ATGTTTAGAATACTT | 7088 |
rs768082840 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629451 | TAAAACAGCCAAAAT[A/C]ATTTTTTAAACCAAA | 7088 |
rs768116378 | snp | A/G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678620 | ACAAGTTCAATACCA[A/G/T]CCTGGCCAACATGGC | 7088 |
rs768118085 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647023 | AGGTTGCCTAAACCC[A/G]AATTTCATGGTTTTT | 7088 |
rs768166595 | snp | C/T | 1.64895e-05 | 0.00287132 | synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81652277 | AACAGCCTGGGCCAC[C/T]TGTTGTTGATGCTTT | 7088 |
rs768173201 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657305 | TTAAGTCTTTATGTG[C/G]TCAAATGAAAGCATT | 7088 |
rs768181198 | snp | C/T | 1.78147e-05 | 0.00298446 | intron-variant | TLE1 | GRCh38.p7 | 9:81591101 | ATTACCGAGCAATCA[C/T]AGCACCATGTTCTCT | 7088 |
rs768197621 | snp | A/G | 3.31483e-05 | 0.004071 | intron-variant | TLE1 | GRCh38.p7 | 9:81613363 | ACAAAGCACAACAAG[A/G]GGCGATGCTGTACCC | 7088 |
rs768204185 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81619399 | ACTACAGCTGGCTCC[A/T]GCAAATCACTGGGAT | 7088 |
rs768221165 | snp | A/C | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686923 | CTTTGCCTCAGAAAA[A/C]CCAATTTTCTAGTAT | 7088 |
rs768281021 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658391 | CTGATGAAAAACATC[A/G]AAAGCCATACCATAT | 7088 |
rs768285731 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81689098 | CACTCGCCCTGCACG[A/G]CCGGACCGGCCGCTC | 7088 |
rs768294495 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680878 | TGAGATGTTGACTTA[-/G]GGGGAAAAAAAATCT | 7088 |
rs768318653 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669636 | ACACCAAAAGACATG[C/T]ACACAAAGAGGAAGG | 7088 |
rs768323292 | snp | A/G | 3.29527e-05 | 0.00405898 | utr-variant-3-prime | TLE1 | GRCh38.p7 | 9:81584192 | ACGTTAAACCACATA[A/G]TGTTTTCAGTAGATG | 7088 |
rs768354564 | in-del | -/AGA | 6.62405e-05 | 0.00575464 | cds-indel | TLE1 | GRCh38.p7 | 9:81616123 | AGGGCTTGCTCGCGG[-/AGA]AGAAGGGTCCTCAAC | 7088 |
rs768369088 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597128 | TGTGTCTGTTTCGTG[A/G]TCCATAAGATAGGAA | 7088 |
rs768401821 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665621 | CAGGGGCCTGCATCT[C/G]CGGAGAAAGCTCTCC | 7088 |
rs768467257 | snp | A/T | 9.90671e-05 | 0.00703731 | missense | TLE1 | GRCh38.p7 | 9:81620459 | GTGGCTGGAGTCCTT[A/T]TCATCCACCTTCCTT | 7088 |
rs768480178 | snp | A/G | 9.32988e-05 | 0.0068294 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611784 | CATGGGGGAGCGCCC[A/G]TAGGCCACCACGGCG | 7088 |
rs768484694 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591614 | ATGAAGGGGCTGTGG[A/G]TGGGGGGCCCTCATA | 7088 |
rs768485790 | snp | C/T | 1.65034e-05 | 0.00287253 | synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81654010 | GACTTGTGCACAAAT[C/T]GTATTCAATCTCTTG | 7088 |
rs768510620 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609364 | TGCTAGGATTATAGG[C/T]GTGAGCCACTGCGCC | 7088 |
rs768523453 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607569 | CTTATTTGCCTGTTA[C/T]TCCACCAAAGGTTCA | 7088 |
rs768583370 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596692 | AAATAATGGACATGG[A/G]AATGACCGCATTTCT | 7088 |
rs768600733 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612227 | ACCAGGAAGCCAGGG[G/T]AATTAAGAGTATTCC | 7088 |
rs768616044 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664589 | TGGGGAGGTCGGGCA[C/G]AGTGGCTCACGCCTA | 7088 |
rs768644506 | snp | C/T | 1.64838e-05 | 0.00287083 | intron-variant | TLE1 | GRCh38.p7 | 9:81616725 | GAAACATTAACGCCA[C/T]TTACTAAAAGCTAAG | 7088 |
rs768662491 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600661 | CTACCCAAATATCAC[-/T]TGTGATGGTCAATTT | 7088 |
rs768667505 | snp | C/T | 1.70023e-05 | 0.00291563 | intron-variant | TLE1 | GRCh38.p7 | 9:81616160 | ATAATCAAAAGTTTT[C/T]GTGATTTAGCTTGTA | 7088 |
rs768669094 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676525 | ACAGGAAAACTCAAA[A/C]CATACTTTCAGCAAG | 7088 |
rs768737906 | snp | C/G | 1.64906e-05 | 0.00287142 | intron-variant | TLE1 | GRCh38.p7 | 9:81584329 | GAAAACAATGGACAT[C/G]TGTTTAATGTGGAAC | 7088 |
rs768759523 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651145 | ATTATCATTACAAAG[C/T]GTCTGAGGGAACTAT | 7088 |
rs768762653 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81635029 | TTTCCCAGAAGGAAT[A/G]AAGGCTCAAAGGCAC | 7088 |
rs768812383 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594647 | AACCATAAACAATAA[A/G]TGAAGTATGCACTGC | 7088 |
rs768830521 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622373 | CACAGCCTTCCAAGC[C/T]CTCCTGCTGTCATCA | 7088 |
rs768898056 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673826 | TAAACCCAAAAAGCC[A/G]ACTTCTGAAAGCCAA | 7088 |
rs768907189 | snp | A/G | 5.67875e-05 | 0.00532828 | intron-variant | TLE1 | GRCh38.p7 | 9:81600092 | TTTCCAAACTTCTCA[A/G]TGTGCTGGGGCAGGA | 7088 |
rs768917550 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660366 | AAAACAAAATCATAC[A/G]TTGGTAAGTATAAAA | 7088 |
rs768934883 | snp | A/G | 6.14723e-05 | 0.00554368 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634276 | CCGTGGCCATGAGAA[A/G]GATGCTGAGCTTGCA | 7088 |
rs768936475 | in-del | -/GA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627844 | CGGTGCTGACATGCT[-/GA]GAGAACCATCAGTAA | 7088 |
rs768940835 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669030 | CCAGAAACCAAATTT[A/C]ACCCACGTATTCTGT | 7088 |
rs768953422 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684854 | ATTAATGCTTTCTTT[C/G]GCAGACAATGACTAC | 7088 |
rs768978270 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610369 | CATCAATACTGTTCA[C/T]TAGAAACTCACAGAT | 7088 |
rs769032646 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612109 | AATCACCTCCAATTT[A/G]TACACTGGATCCCTC | 7088 |
rs769059586 | snp | C/G/T | 0.000234902 | 0.0108351 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587634 | AGGAGGAAGACACAC[C/G/T]CCAGCCACCTCCCAG | 7088 |
rs769092655 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586211 | TTTAGTAAAGACGGG[A/G]TTTCACCGTGCCAGC | 7088 |
rs769133556 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674217 | CAGCAAGTCACTTGT[A/G]TTCTGTAATACATTT | 7088 |
rs769136766 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680684 | CACCTCGGAATCTAG[C/G]CTCTAAATGCAGAGA | 7088 |
rs769148960 | snp | A/T | 2.40897e-05 | 0.00347049 | intron-variant | TLE1 | GRCh38.p7 | 9:81620937 | CTTGAGATTACTCTA[A/T]TAGACATATTCTTTA | 7088 |
rs769166830 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599142 | AGAAAACTATGAAGC[A/G]CAATATAGTCAACCT | 7088 |
rs769167514 | snp | A/G | 5.02635e-05 | 0.0050129 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685924 | AACAGGCAACTTAAT[A/G]TAAACATTATGTCAC | 7088 |
rs769189109 | snp | C/G | | | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590454 | CAAGTTCTAGCCAAA[C/G]CCCAAAACATCTAGT | 7088 |
rs769204458 | in-del | -/AG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627167 | CAAAGATGAGGACAC[-/AG]AGTTTGTTGTCCACC | 7088 |
rs769228308 | snp | C/G | 1.65386e-05 | 0.00287559 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585626 | CACTGCCAGCCACTC[C/G]CCGGTGGGGCAGTAC | 7088 |
rs769276934 | snp | A/G | 1.65102e-05 | 0.00287312 | intron-variant | TLE1 | GRCh38.p7 | 9:81584345 | TGTTTAATGTGGAAC[A/G]ACGGTACTCAGAGGC | 7088 |
rs769286245 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617825 | GGTCAGGAGCTCGAG[A/G]CCAGCCTGGACAACA | 7088 |
rs769295200 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640594 | AAACAAATGCCAAAC[C/G]CTGAGTTAATGATAC | 7088 |
rs769309657 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668700 | ACACATAATTAAAAG[C/T]ATGCCAAAAAAAAGG | 7088 |
rs769316255 | snp | A/T | 1.98789e-05 | 0.00315263 | intron-variant | TLE1 | GRCh38.p7 | 9:81610176 | TAATACCAATGACTG[A/T]GTAACCACCTTTAAA | 7088 |
rs769327630 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591439 | TTTCGGTCTTCGTTA[C/T]GCTGAGCACATTACC | 7088 |
rs769377679 | snp | C/T | 6.59946e-05 | 0.00574395 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81620465 | GGAGTCCTTATCATC[C/T]ACCTTCCTTTTCTTG | 7088 |
rs769382201 | snp | A/G | 3.2956e-05 | 0.00405918 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593214 | GGGTCCGATGAGGGC[A/G]TCGGGGGGAAAAGGG | 7088 |
rs769397273 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642407 | AATGAAATTGGGGTC[C/T]GAGGTCCGGGCACAG | 7088 |
rs769400603 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629063 | CCTTACATTCAACAA[A/G]TGTTTAACTGTGACA | 7088 |
rs769413025 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669591 | GTACATGCAAATATA[G/T]GCATGCTTACACCTC | 7088 |
rs769415366 | snp | A/C/G | 4.94632e-05 | 0.00497288 | missense | TLE1 | GRCh38.p7 | 9:81584506 | AGGTTATCTTTTCCA[A/C/G]TACTCACAAACCATT | 7088 |
rs769460525 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640383 | AGCTGATTCCACTAA[C/T]AATTTCAAAAATTAA | 7088 |
rs769469998 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | TLE1 | GRCh38.p7 | 9:81593119 | GTGTACACGTGTCTC[A/G]TGGGGTTGCTGATGG | 7088 |
rs769485994 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656364 | GGTCCTTGCTCCCAA[A/C]TCCCTACCTACCACA | 7088 |
rs769489349 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639389 | ACTCTCTAACCAAAA[C/T]CTGCCCGTCATTTGG | 7088 |
rs769500401 | snp | A/G | | | missense | TLE1 | GRCh38.p7 | 9:81616100 | CCATTTTCCCGGGGC[A/G]AGTGGGCAGGGCTTG | 7088 |
rs769501789 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606670 | TTAGGAGAAATACCT[A/G]ATGTAAATAACGAGT | 7088 |
rs769507753 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606522 | AAACTATCACAAGCA[C/G]AAGGACAGAAAACCA | 7088 |
rs769512720 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676262 | TCTGGATAACTCATC[A/G]GGAAGGGTAGATGGA | 7088 |
rs769518153 | snp | C/T | 1.65149e-05 | 0.00287353 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590816 | TCACCTCACTAGTGT[C/T]TGGTTGTGCAGATCC | 7088 |
rs769535384 | snp | A/G | 2.18782e-05 | 0.00330736 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688253 | CATCGCTCTGGCGGC[A/G]GCCGGGGCTCTGTTC | 7088 |
rs769574669 | in-del | -/CTG | 1.66136e-05 | 0.00288211 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685773 | CATGTTTTTTACACT[-/CTG]CTAACACGTTTGCTA | 7088 |
rs769590187 | snp | C/G | 1.90511e-05 | 0.00308629 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688180 | AAGCGCCTCCCCAAC[C/G]ATCCTGGCCCCCCAC | 7088 |
rs769608628 | snp | A/C | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686751 | AAGAAACTAAGGCTG[A/C]GATGGATATAAATGT | 7088 |
rs769643581 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633026 | AATGCAACCATTAAC[A/C]CTTTTAAAGTGAGGC | 7088 |
rs769689735 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671438 | ATCACAAGGTCAGGA[-/G]GTTCAAGACCAGCCT | 7088 |
rs769731737 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603728 | GATACAAGGTCAGGC[A/G]TGGTGGCTCATGCCT | 7088 |
rs769767099 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596418 | CAAAGGGTGGATGGG[C/T]CTTTAGGAGGGATCA | 7088 |
rs769773950 | snp | A/C | 2.1907e-05 | 0.00330954 | missense | TLE1 | GRCh38.p7 | 9:81611792 | AGCGCCCGTAGGCCA[A/C]CACGGCGGCCGCGGC | 7088 |
rs769781352 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674543 | ATACACACAAAGTTC[-/A]AAATCAGAGTCCTTT | 7088 |
rs769800949 | snp | C/G | 1.82727e-05 | 0.00302258 | intron-variant | TLE1 | GRCh38.p7 | 9:81610315 | GAAACAAAAATAAGG[C/G]ATTGCAGACTCAGTT | 7088 |
rs769808084 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646730 | ACTCAATCTCTTAGG[A/G]ATAGACAGGCTCCTT | 7088 |
rs769824968 | in-del | -/TTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626506 | TAATGAGATCCCCAC[-/TTG]TTAACAACATGGACA | 7088 |
rs769850067 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601832 | ATCTCCTTTAGAAAA[G/T]AATGAATCACAGGAT | 7088 |
rs769857436 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646019 | GGAATCAAGTAAAAA[G/T]CACAGGAAACTATGT | 7088 |
rs769857494 | snp | A/G | 1.64909e-05 | 0.00287144 | missense | TLE1 | GRCh38.p7 | 9:81620541 | CTTAGACTGTCTGGG[A/G]CCAGGAGGGAATTAC | 7088 |
rs769891125 | snp | A/G | 1.64838e-05 | 0.00287083 | intron-variant | TLE1 | GRCh38.p7 | 9:81616718 | GAAAAAAGAAACATT[A/G]ACGCCATTTACTAAA | 7088 |
rs769905907 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644121 | CATGTAGAGAAATTG[C/G]AATTCTCGTACGCTA | 7088 |
rs769947595 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602526 | GATACCAAATAAACT[A/G]TGTGTTGTGTGTTTT | 7088 |
rs769954659 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643162 | AAGGTACAACACGGT[A/G]ACTATAGTTAATAAT | 7088 |
rs769960265 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632388 | AGCTACTATTCTACA[A/C]AGAAGAGGGGGGAAA | 7088 |
rs769970906 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669146 | CCTGCCATTTGGACT[G/T]TGAAACACAGTAATC | 7088 |
rs770009768 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654642 | CACTGCACCCAGCCA[A/T]GTGTACTTTTTCAAT | 7088 |
rs770036980 | snp | C/G | 1.67416e-05 | 0.00289318 | intron-variant | TLE1 | GRCh38.p7 | 9:81585666 | AAGATCTACAAGGAG[C/G]AAGACAGGCTCACTC | 7088 |
rs770055961 | snp | A/G | 3.44691e-05 | 0.00415131 | intron-variant | TLE1 | GRCh38.p7 | 9:81616173 | TTCGTGATTTAGCTT[A/G]TAACAGACAGACTTT | 7088 |
rs770061768 | in-del | -/AATAAAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666809 | ATAAATAAATAAATA[-/AATAAAT]AAATAAAATATGCCT | 7088 |
rs770077557 | in-del | -/TT | 1.65842e-05 | 0.00287955 | intron-variant | TLE1 | GRCh38.p7 | 9:81613360 | AAACAAAGCACAACA[-/TT]AGAGGCGATGCTGTA | 7088 |
rs770089715 | snp | C/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690914 | GATTGTAATAATCAA[C/G]ACATGCTGTATAATT | 7088 |
rs770153097 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585135 | CCTAAATATCGACTT[C/T]TCTAACCCTGGATTC | 7088 |
rs770167622 | in-del | -/GGCT | 1.71018e-05 | 0.00292414 | frameshift-variant | TLE1 | GRCh38.p7 | 9:81593266 | CAGTAACGTGGAAGG[-/GGCT]AGTATGCACTTTTGG | 7088 |
rs770216888 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659231 | TGACTCCTGCCCATG[C/T]TTCTATTCTTGATTG | 7088 |
rs770217805 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623009 | AATTGCCCCTGACTT[C/G]TTCCAGCCCTGACGC | 7088 |
rs770252630 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610111 | GAAAAGACACCAGAA[A/G]TCTCCTTGGAAACGC | 7088 |
rs770279950 | snp | A/G | 1.65162e-05 | 0.00287365 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81613379 | GGCGATGCTGTACCC[A/G]CTTGGTTAACGAGGG | 7088 |
rs770285958 | snp | A/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690153 | CAGATCTAAGTGAAA[A/G]TAACTCAAAGACTAG | 7088 |
rs770361802 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613015 | GTGAGCTGAGATCCC[A/G]CCATTGCATTCCAGC | 7088 |
rs770384924 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627790 | GAAATTTGATTATCA[A/G]GAAAGTGATCACGTT | 7088 |
rs770411615 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680178 | TCATTATACAGAGAG[A/G]GGAACTGAAGCCAGG | 7088 |
rs770416469 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681413 | AAATTAGCCAGGCAT[A/G]GTGGTGGACTCCTGT | 7088 |
rs770427719 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81608837 | AGCTACTCGAGAGGC[C/T]GAGACAGAAGAATTG | 7088 |
rs770431495 | in-del | -/AG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621141 | GAAATTTAAGATCTA[-/AG]GGGGGAATTTCAGCC | 7088 |
rs770436597 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683936 | CATCCCGCCACATAA[A/C]CTACAGGAACCCAGA | 7088 |
rs770449303 | snp | A/T | 1.7172e-05 | 0.00293013 | intron-variant | TLE1 | GRCh38.p7 | 9:81585701 | TTCCGCCTGATACAC[A/T]TAGGAAGGGAAGACG | 7088 |
rs770455172 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659550 | CAGGATGAAGGCTCC[A/T]GCAACAAGACTTTCT | 7088 |
rs770478908 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678743 | CTGCTTGAACCTACA[C/T]ACCTGTAATCCCGGC | 7088 |
rs770500621 | snp | A/G | 1.66214e-05 | 0.00288278 | intron-variant | TLE1 | GRCh38.p7 | 9:81585493 | CTCCAGTTTCCTTTC[A/G]GCTGAACTCACCACA | 7088 |
rs770501348 | snp | A/G | 3.33996e-05 | 0.0040864 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685725 | ATTTCATAATACTGT[A/G]AAGAGAAAAAAGAAT | 7088 |
rs770509372 | snp | C/G | 0.000126807 | 0.00796162 | intron-variant | TLE1 | GRCh38.p7 | 9:81600053 | TCTGAGTTCTAGGAC[C/G]TAACTTCCTCTATCA | 7088 |
rs770520549 | snp | C/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691313 | TGTTGGAGTTGTTTT[C/T]AAATATGTATGATAT | 7088 |
rs770527779 | in-del | -/ACTTAAAAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620729 | TCTACAGGTTTACAC[-/ACTTAAAAG]GGAGACCCTGACTTT | 7088 |
rs770531705 | snp | C/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690092 | TGAGGGCTCGAGTTA[C/G]CAAAAATCCTGCCAC | 7088 |
rs770590564 | snp | A/C/T | 4.96433e-05 | 0.00498192 | intron-variant | TLE1 | GRCh38.p7 | 9:81584537 | TACCTAGAATTAGCA[A/C/T]AGGAATATCTAGTTT | 7088 |
rs770610621 | snp | C/T | 1.72317e-05 | 0.00293523 | missense | TLE1 | GRCh38.p7 | 9:81611834 | TCATCTGGGGCGACA[C/T]GTTGTGTAAACTGGC | 7088 |
rs770614478 | in-del | -/AG | 1.66985e-05 | 0.00288946 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685727 | TTCATAATACTGTAA[-/AG]AGAAAAAAGAATCAA | 7088 |
rs770656244 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685801 | TGCTAATATCATATG[A/G]AAAAGGAAAAAGTCC | 7088 |
rs770657561 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612736 | TTATCAGAAACTTTA[-/C]TGAAGTCCCTAGGAT | 7088 |
rs770663932 | snp | A/G | 1.66715e-05 | 0.00288712 | intron-variant | TLE1 | GRCh38.p7 | 9:81652172 | TAAGAAATGAAAGCT[A/G]GTTATACACACTGTA | 7088 |
rs770695103 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645419 | AATTTTAAAATAACT[A/G]AAAGCGTGTCATTAG | 7088 |
rs770700517 | snp | C/T | 3.30278e-05 | 0.0040636 | missense | TLE1 | GRCh38.p7 | 9:81620553 | GGGACCAGGAGGGAA[C/T]TACTCTGCAAGACAA | 7088 |
rs770732902 | snp | A/C/T | 1.65111e-05 | 0.0028732 | utr-variant-3-prime | TLE1 | GRCh38.p7 | 9:81584148 | CTATTTCTATAAATT[A/C/T]GAAACATTTTGGCCC | 7088 |
rs770808570 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651500 | AAAAGCCAGGGAGCA[-/C]TAGGGCAGACAATTA | 7088 |
rs770817751 | in-del | -/TAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675330 | TATGTAAAGACTAAG[-/TAAA]TAAATAATCAGTGGT | 7088 |
rs770820959 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594936 | GCAAAATATCAGACA[C/T]ATGAAGACTTTTAAA | 7088 |
rs770822821 | snp | A/G | 1.72877e-05 | 0.00293999 | intron-variant | TLE1 | GRCh38.p7 | 9:81591076 | TAAACATAATTCATT[A/G]CTATAATGAATTACC | 7088 |
rs770838903 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616554 | GAGGTCCCCCCACCG[A/T]GGGGCTCTACTTCCT | 7088 |
rs770839836 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684890 | CGAGGGTCCTTTGGG[C/T]TGAGCAATCATTTAG | 7088 |
rs770937009 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590849 | CACAGCGATGTTGCC[A/G]TCGCTGCAGCATGAG | 7088 |
rs770943118 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81593394 | AGATTCTCTTGTATA[C/G]TTTCCTTTGAAATCA | 7088 |
rs770954350 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668906 | ACAAGTTATTTTACA[A/C]GTGGACAAATCAATT | 7088 |
rs770962666 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601718 | GTTATGCTGAACTAA[A/G]CAATACCAATTAAAT | 7088 |
rs770964001 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671852 | GGCCTTTGGTCAGCT[-/A]AAAAAGTACAGAAGT | 7088 |
rs770981636 | snp | A/T | 1.64942e-05 | 0.00287173 | missense, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587743 | CCCAGGACCTGACTG[A/T]GTTGTCCAAACCACC | 7088 |
rs770986519 | in-del | -/GC | 0.499808 | 0.00980204 | intron-variant | TLE1 | GRCh38.p7 | 9:81633324 | TGTGTGTGTGTGTGT[-/GC]GCAGCAGGCGTTTGA | 7088 |
rs771002473 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644814 | GCCTGGCCAATATGG[A/T]GAAACCCCATCTCTA | 7088 |
rs771017273 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668560 | TATACAATCCACAGA[C/G]GAATCTAAGTAAGAG | 7088 |
rs771017837 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81613088 | GGCAGAGGTTGCAGT[A/G]AGCTGAGATCACGCC | 7088 |
rs771052256 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673739 | CGGACCAATTCCTAG[G/T]GCACATGGGAGCTCC | 7088 |
rs771080523 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683108 | TGACACTGAAATCTC[C/T]AGAACTCACTCCGAC | 7088 |
rs771086980 | snp | A/C | 0.000102597 | 0.00716158 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687478 | GGACGGGAATGCGGG[A/C]GGATGAATAAAGCAG | 7088 |
rs771108625 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641976 | GCAGTAAGCGGAGAT[A/C]GCGCCATTGCACTCC | 7088 |
rs771145941 | snp | A/C | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588402 | TTCTGTGTTAGAAAG[A/C]GCCCTGCATTAGGAA | 7088 |
rs771152589 | in-del | -/CGAC | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688950 | TCGGCACGCCCCGTG[-/CGAC]CGACCAGCACTCGGT | 7088 |
rs771177201 | snp | G/T | 5.79537e-05 | 0.0053827 | intron-variant | TLE1 | GRCh38.p7 | 9:81610335 | CAGACTCAGTTTATT[G/T]CAGCAGGCACTTTGT | 7088 |
rs771246202 | snp | C/G | 9.78043e-05 | 0.00699232 | missense, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687431 | CTGCAGCCTGGTGCG[C/G]CGTCTGGGGGCGACC | 7088 |
rs771274253 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681146 | ACATGGCCTGAGATG[C/T]TGCTTGCTGAAATAT | 7088 |
rs771285560 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592789 | GAGCCTCTGTAAACC[A/G]CTGTAAAATATTTTT | 7088 |
rs771286660 | snp | A/C | 1.65326e-05 | 0.00287507 | synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81654034 | TCTCTTGGCGATTTC[A/C]GTCTATAAAGACAAA | 7088 |
rs771357821 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679183 | AAATAATGAAACATG[C/T]AATTTTGCTAAATCA | 7088 |
rs771364039 | snp | A/G | 1.65209e-05 | 0.00287405 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593244 | GACAGGCTGCATCTG[A/G]CCGTCTGCAGTAACG | 7088 |
rs771375814 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671334 | GCCTGGGCAACATGG[C/T]GAAACCCTGTCTCTA | 7088 |
rs771382662 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659473 | AACAACAATAAATCT[A/G]CATTCAAGAGCTATC | 7088 |
rs771448081 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672516 | AGCAGCAGCTGTGAA[C/T]CTTGACTGTCAACAA | 7088 |
rs771456157 | in-del | -/C | 3.3998e-05 | 0.00412284 | intron-variant | TLE1 | GRCh38.p7 | 9:81590780 | AAGAAGCGAACCCCT[-/C]CCTTAGACGACCATC | 7088 |
rs771460239 | snp | A/G | 3.38078e-05 | 0.00411129 | intron-variant | TLE1 | GRCh38.p7 | 9:81613569 | TTTTTAATCCAAGCC[A/G]TATTACACAATTTAT | 7088 |
rs771474904 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633157 | AAGACAAGAGCAGAG[C/T]GAACAGTCATATAAG | 7088 |
rs771485694 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602346 | TCCAAAATGCTTCAG[A/G]ACCAGAAGTGTTTCT | 7088 |
rs771555750 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620627 | GAAACCCAACCTCGA[C/T]GTGAGAACTATTTTT | 7088 |
rs771573048 | snp | C/T | 3.94438e-05 | 0.00444076 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634198 | AGGCCGGCACTGCCC[C/T]CGAGGGGCGGGATTC | 7088 |
rs771631477 | snp | C/T | 2.33626e-05 | 0.00341771 | intron-variant | TLE1 | GRCh38.p7 | 9:81620923 | GCCTATGAGCAAATC[C/T]TGAGATTACTCTATT | 7088 |
rs771634197 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637329 | TGCCACTGCACTCCA[-/G]CCTGGGTGACAAGAG | 7088 |
rs771638847 | in-del | -/GTGC | 8.99645e-05 | 0.00670628 | intron-variant | TLE1 | GRCh38.p7 | 9:81633322 | TGTGTGTGTGTGTGT[-/GTGC]GTGCAGCAGGCGTTT | 7088 |
rs771676377 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680580 | CCAGGACAAAAACCA[-/G]CCACTGGCCCACTGC | 7088 |
rs771685950 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678927 | AGGTGGATCACCTGA[A/G]GCTAGGAGTTTGAGA | 7088 |
rs771689269 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606850 | AGATCCTGGCAACAA[C/T]GGCAAAGTTCATTTT | 7088 |
rs771725568 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671480 | TGAAACCCCACCTCT[A/T]CTAAAAATACAAAAA | 7088 |
rs771726730 | in-del | -/A | 4.94466e-05 | 0.00497201 | intron-variant | TLE1 | GRCh38.p7 | 9:81616704 | CCATCACTGTCCTGG[-/A]AAAAAGAAACATTAA | 7088 |
rs771733959 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664709 | TCTCTTTTAATTAAG[-/A]AAAAAAAAAAATAAG | 7088 |
rs771742481 | snp | C/T | 0.00086097 | 0.0207303 | intron-variant | TLE1 | GRCh38.p7 | 9:81633333 | TGTGTGTGCAGCAGG[C/T]GTTTGAGTACTTACT | 7088 |
rs771770027 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656004 | TTTAGTCTGACCCAA[C/T]CCAATTCTCCCTGAC | 7088 |
rs771811133 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628855 | GTGGTGCTTAGACTG[G/T]TCTGAGTTAGGAAGC | 7088 |
rs771831886 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595817 | GAGACTCTGTCTCAA[-/A]AAAAAAAAAAAAAAA | 7088 |
rs771899498 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81652257 | GTCACCTGTTTGGCA[C/T]GTTCAACAGCCTGGG | 7088 |
rs771974961 | in-del | -/TGTGTGTGTG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662364 | AGTGTGCCTGTTTTG[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 7088 |
rs771990328 | snp | A/G | | | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616129 | TGCTCGCGGAGAAGA[A/G]GGGTCCTCAACAAGC | 7088 |
rs771993655 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642097 | AAAAAGACAAAGATA[-/G]TGTTAGTGATGGTGT | 7088 |
rs771995074 | snp | C/T | 1.73754e-05 | 0.00294744 | intron-variant | TLE1 | GRCh38.p7 | 9:81616181 | TTAGCTTGTAACAGA[C/T]AGACTTTTCCCTTTC | 7088 |
rs771995140 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586878 | AACAAAATGTTAACA[A/G]GAATATGAAATTTAG | 7088 |
rs772009674 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687656 | CTCTTCCCAGTCTCC[A/G]GGGCGGATTGCGCTA | 7088 |
rs772024968 | snp | C/G | | | missense | TLE1 | GRCh38.p7 | 9:81593070 | ATTGCCAGGGTGGCT[C/G]ATGTCCCAGACCTTG | 7088 |
rs772026613 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654938 | AGGGTGATGGTCAAG[C/T]CATGATATCCTGAGT | 7088 |
rs772033823 | in-del | -/AAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615120 | AAAAAAAAAAAAAAA[-/AAG]AAGAAGAAGAAGAAG | 7088 |
rs772049274 | snp | A/G | 0.000197687 | 0.00994004 | missense | TLE1 | GRCh38.p7 | 9:81584292 | CAGCTAAGCACTGAC[A/G]AGGACTCTTTGGACT | 7088 |
rs772058186 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597894 | AAGGGGGCAGGTTGT[G/T]TTTTCCTAGCAGACC | 7088 |
rs772061367 | in-del | -/CTC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669566 | GGCATGTGCCAAAAT[-/CTC]CTCACTTGTACATGC | 7088 |
rs772061478 | snp | A/G | 1.65608e-05 | 0.00287752 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81652185 | CTGGTTATACACACT[A/G]TAGGAGGTAGACCTG | 7088 |
rs772065570 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665931 | CAATGCTGTTTGTGT[A/T]AATTTTTCCCCCTTC | 7088 |
rs772157623 | snp | A/G | 3.52553e-05 | 0.00419838 | intron-variant | TLE1 | GRCh38.p7 | 9:81591092 | CTATAATGAATTACC[A/G]AGCAATCATAGCACC | 7088 |
rs772185102 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624404 | AGGCTTCATGGCATG[C/G]CAATCACCAGAGGTA | 7088 |
rs772196333 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81585968 | CTGAAATACGATCAT[A/G]TATCACCTATCAAGG | 7088 |
rs772254243 | in-del | -/G | 1.66098e-05 | 0.00288177 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685900 | TCCAATTTAAGGCTA[-/G]GAAAACAAAACAGGC | 7088 |
rs772301697 | snp | A/G | 1.65206e-05 | 0.00287403 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585608 | ATTGCTGCTCTCCAT[A/G]CCCACTGCCAGCCAC | 7088 |
rs772303386 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587772 | CCCGTCCAGAGCTTG[A/G]TGCCATCATTAGAAA | 7088 |
rs772311750 | snp | C/T | 0.000328863 | 0.0128189 | missense | TLE1 | GRCh38.p7 | 9:81611816 | CCGCGGCGGCTGCGG[C/T]GCTCATCTGGGGCGA | 7088 |
rs772315757 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674874 | AAAATGTACATGGAC[A/G]CCAGGTGTGGTGGCT | 7088 |
rs772355339 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591743 | CTTCAACAAAGGATA[C/T]TCCTACTGCTATAGA | 7088 |
rs772380100 | snp | C/T | 1.65573e-05 | 0.00287721 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685887 | CAGTTTCTCACATTC[C/T]AATTTAAGGCTAGGA | 7088 |
rs772420250 | snp | A/C/G | 8.03479e-05 | 0.00633788 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634202 | CGGCACTGCCCCCGA[A/C/G]GGGCGGGATTCCAGG | 7088 |
rs772458958 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653406 | CAGTTTCATAGATTA[C/T]TCATATAAAGAGATT | 7088 |
rs772468001 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81619810 | TGGATCTGTGACAAG[A/G]GCCCTCACTCCATCA | 7088 |
rs772479132 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81595658 | CCCATCTCTACTAAA[A/T]ATACAAAAAAATCAG | 7088 |
rs772503157 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614901 | GAAGACTTAAGAATC[-/T]CGGAAGTTTGAGGCC | 7088 |
rs772514871 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612828 | TTTGGGAGGCCGAGA[C/T]GGGCAGATCACCTGA | 7088 |
rs772520729 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601436 | GATTTCTAAATTACA[C/T]GTCTGGCATTAAAAC | 7088 |
rs772527523 | in-del | -/CA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650331 | TGAGAATTTAAACGT[-/CA]GAGTTTTGCCATCAT | 7088 |
rs772529760 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638647 | TTTTCTTTTTTTGAG[A/T]CAGAGTCTTCACTGT | 7088 |
rs772537705 | snp | A/C | 1.66821e-05 | 0.00288804 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685741 | AAGAGAAAAAAGAAT[A/C]AAGCATTTCATTAAC | 7088 |
rs772541697 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669882 | CTTTTTAAAGATAAT[A/G]TTGTACCACATATAA | 7088 |
rs772553167 | snp | G/T | 4.95544e-05 | 0.00497742 | missense | TLE1 | GRCh38.p7 | 9:81585520 | CACAGTAAGCAAATT[G/T]CAGGGACAGCACGCA | 7088 |
rs772571832 | snp | C/T | 5.89154e-05 | 0.00542717 | intron-variant | TLE1 | GRCh38.p7 | 9:81600073 | TTCCTCTATCAATTA[C/T]ACGTTTCCAAACTTC | 7088 |
rs772710961 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626506 | TAATGAGATCCCCAC[C/T]TGTTAACAACATGGA | 7088 |
rs772773720 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644760 | GCACTTTGGGAGGCA[A/G]AGACAGGTGAATCAC | 7088 |
rs772775029 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606955 | TAGGCCAGGCATGGT[A/G]GCTCATGCCTGTAGT | 7088 |
rs772778878 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597380 | GGAGGAAGACGCAGG[G/T]TGGGGATCAGGAAAG | 7088 |
rs772806043 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666067 | ATCACAGCTGTTTTA[A/G]TTCCTAAATAGCACA | 7088 |
rs772829716 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596725 | AATTTCGAACACAGG[C/T]AAAATTCATCTGCAG | 7088 |
rs772859433 | in-del | -/GCAGCAGGC | 0.000453123 | 0.0150451 | intron-variant | TLE1 | GRCh38.p7 | 9:81633325 | TGTGTGTGTGTGTGT[-/GCAGCAGGC]GTTTGAGTACTTACT | 7088 |
rs772868976 | snp | A/G | 7.48307e-05 | 0.00611635 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634292 | GATGCTGAGCTTGCA[A/G]CTGCTGCTGCTGTTG | 7088 |
rs772879890 | snp | G/T | 1.64874e-05 | 0.00287113 | missense | TLE1 | GRCh38.p7 | 9:81620476 | CATCCACCTTCCTTT[G/T]CTTGATGTCATTGGA | 7088 |
rs772884960 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636120 | TGAGGTCAGAACAGG[A/C]AGCATTCATAGCATT | 7088 |
rs772889154 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648480 | GCTGTGCATTTCACT[A/G]TATTACAATTATACA | 7088 |
rs772905325 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637828 | GTGTCCATCGTCTGG[C/T]ACAAGCTTGGAACAC | 7088 |
rs772944934 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620638 | TCGATGTGAGAACTA[C/T]TTTTGAAAGGTGATA | 7088 |
rs772956698 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669624 | CCCTCCCCCCCCACA[A/C]CAAAAGACATGCACA | 7088 |
rs772977663 | snp | C/T | 3.30316e-05 | 0.00406383 | intron-variant | TLE1 | GRCh38.p7 | 9:81584347 | TTTAATGTGGAACAA[C/T]GGTACTCAGAGGCCC | 7088 |
rs772994167 | snp | A/G | 4.39377e-05 | 0.00468689 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688254 | ATCGCTCTGGCGGCG[A/G]CCGGGGCTCTGTTCC | 7088 |
rs772996825 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598059 | GAGAGGACGGCTGTG[A/G]TCAAGCCCCGCTGCC | 7088 |
rs773013517 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643393 | AGGCATGTGCCACCA[C/G]GCCAGGCTAATTTTG | 7088 |
rs773036068 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592162 | AGGAGATCGAGACCA[G/T]TCTGGCTAACATGGT | 7088 |
rs773041252 | in-del | -/ATT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672323 | TCTCCCCTGCAATAA[-/ATT]ATTATTATTATTATT | 7088 |
rs773044077 | snp | A/G | 6.60906e-05 | 0.00574812 | synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81654028 | ATTCAATCTCTTGGC[A/G]ATTTCAGTCTATAAA | 7088 |
rs773044457 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627713 | TCTTAACATGTCAGG[A/T]CATGATTAATTCATA | 7088 |
rs773045135 | snp | C/T | 1.64933e-05 | 0.00287165 | intron-variant | TLE1 | GRCh38.p7 | 9:81615974 | AAGTGTCAGTTTTCT[C/T]TACCTACCAAGCTCA | 7088 |
rs773061485 | snp | A/G | 4.95413e-05 | 0.00497677 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634207 | CTGCCCCCGAGGGGC[A/G]GGATTCCAGGAGGCT | 7088 |
rs773069439 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655464 | GCAAGAGAGGGAACA[A/G]AGGGTACTCTACTTC | 7088 |
rs773082077 | snp | C/T | 1.91565e-05 | 0.00309482 | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688188 | CCCCAACGATCCTGG[C/T]CCCCCACCACCACCC | 7088 |
rs773094615 | snp | A/G | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589523 | GTATTTACTCCCCAG[A/G]AGCCGGCACGGAGCA | 7088 |
rs773129281 | in-del | -/ATA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675285 | AATTTGAAATTTTTC[-/ATA]ATAAAATGTTTGGGA | 7088 |
rs773149502 | snp | C/T | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588633 | TCTGCTGAGCACAGA[C/T]GCTGTGCAAGGCAAC | 7088 |
rs773182013 | snp | A/G | 3.29739e-05 | 0.00406028 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590840 | CAGATCCCACACAGC[A/G]ATGTTGCCGTCGCTG | 7088 |
rs773199479 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602898 | GCTCAGATGTCAGAG[A/G]GAATGGGAATGATGC | 7088 |
rs773201408 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81616517 | TGAGCAACCATTAAC[G/T]TCTTAATGTAAGAAG | 7088 |
rs773242043 | in-del | -/AAG | 1.64857e-05 | 0.00287099 | intron-variant | TLE1 | GRCh38.p7 | 9:81616738 | CATTTACTAAAAGCT[-/AAG]AATAGGTTTGAGGCA | 7088 |
rs773254946 | snp | C/T | 3.36604e-05 | 0.00410232 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685934 | TTAATGTAAACATTA[C/T]GTCACTTGTTTTAAC | 7088 |
rs773263952 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658536 | TATACTGACAAGCCA[G/T]CTTGACTTTTGAGCC | 7088 |
rs773264803 | snp | A/G | 3.47808e-05 | 0.00417003 | missense | TLE1 | GRCh38.p7 | 9:81611830 | GCGCTCATCTGGGGC[A/G]ACATGTTGTGTAAAC | 7088 |
rs773288198 | snp | A/G | 1.67635e-05 | 0.00289507 | intron-variant | TLE1 | GRCh38.p7 | 9:81585668 | GATCTACAAGGAGCA[A/G]GACAGGCTCACTCAT | 7088 |
rs773299476 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653416 | GATTACTCATATAAA[A/G]AGATTCCTCCCTCAA | 7088 |
rs773308221 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671519 | GCGTGGTGGCATGTG[C/T]CTGTAATCCCAGCTA | 7088 |
rs773309550 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682098 | TACAAAAAAAAGAAA[A/G]AAAAAGTTAGCCGGG | 7088 |
rs773326859 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636577 | TACAGGGTGGAGGAT[A/G]CCACCCTCTCACCCC | 7088 |
rs773327669 | snp | C/T | 3.29843e-05 | 0.00406092 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81633358 | CTTACTGTGCCCGGC[C/T]CTCTGTCTGCTCCCG | 7088 |
rs773343619 | snp | A/C | 5.72066e-05 | 0.0053479 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687345 | GCACCTGTGATACTG[A/C]GCCTGCAGGAACTGG | 7088 |
rs773369890 | snp | C/T | 3.79499e-05 | 0.00435586 | intron-variant | TLE1 | GRCh38.p7 | 9:81610198 | ACCTTTAAAACAAAA[C/T]CAAGGTCTTTGAGGT | 7088 |
rs773385579 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640882 | CACCTTCTCCTGACC[A/G]GAAACTAAGCTCCTT | 7088 |
rs773389143 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624509 | AAACAGGATTCATCA[A/G]GTAGAATTCATTTTT | 7088 |
rs773393675 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81610639 | CTATTGACATTTGGG[A/G]CCAAACAGTTCTTTT | 7088 |
rs773466057 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670945 | AGGCCGAGGCAGATG[A/G]ATCACCTGAGGTCAG | 7088 |
rs773477051 | in-del | -/TAATG | 1.67304e-05 | 0.00289222 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685920 | ACAAAACAGGCAACT[-/TAATG]TAAACATTATGTCAC | 7088 |
rs773512123 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658736 | CTAGCTCTCCAAGAG[A/G]ACTTCATGAACATCT | 7088 |
rs773519377 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678956 | GACCAGCCTGGACAA[C/T]ATGCAGAAACCCCAT | 7088 |
rs773528487 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81647189 | TGGCATTTTGTGGAC[A/G]GGAGGACAGTCCCCA | 7088 |
rs773539704 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601555 | TAAGGCAGGTAGAGC[A/C]CAGCCCCCAGGTATT | 7088 |
rs773585815 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | TLE1 | GRCh38.p7 | 9:81613472 | GTTGGCATGTCGCTC[C/T]GAGGCGTTGGTGTGC | 7088 |
rs773605381 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677066 | ACATGGAGAAACCCC[A/G]TCTCTACCAAAATGT | 7088 |
rs773629395 | snp | A/C | 7.11415e-05 | 0.0059637 | intron-variant | TLE1 | GRCh38.p7 | 9:81634054 | TTGCAGCACTGTAAG[A/C]GTATGAGGACAAAGT | 7088 |
rs773658467 | in-del | -/AGTA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630502 | TTTTCTTTCTTACCC[-/AGTA]AGTATCAAAAATCAA | 7088 |
rs773662079 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682854 | CCAAGAAAAAAATAT[A/T]CTTAGTGCTACCATG | 7088 |
rs773670574 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648180 | GGGCGGCTGAGGCAG[A/G]AGAATCACTGGAACC | 7088 |
rs773709683 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644763 | CTTTGGGAGGCAGAG[A/G]CAGGTGAATCACCTG | 7088 |
rs773729520 | snp | C/T | 2.24469e-05 | 0.00335007 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688261 | TGGCGGCGGCCGGGG[C/T]TCTGTTCCCCGGCAA | 7088 |
rs773745224 | snp | A/C | 1.65108e-05 | 0.00287317 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81613380 | GCGATGCTGTACCCG[A/C]TTGGTTAACGAGGGG | 7088 |
rs773776863 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655744 | TGACCTTGAGAAATA[A/G]AGAATGGAAAAAGAC | 7088 |
rs773776953 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81600128 | GCTCCTAAACAGGAC[A/G]AAGATACAAATGGAG | 7088 |
rs773824092 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669898 | TTGTACCACATATAA[C/G]TTTAGGCCCCCACAG | 7088 |
rs773847827 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631698 | CTAGAATAAGTTCAA[C/T]AGATTTAAAACGCAT | 7088 |
rs773900803 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641897 | TGTGGTGGCGCATGC[C/T]TGCAATCCCAGCTAC | 7088 |
rs773902127 | in-del | -/C | 0.000263841 | 0.0114826 | intron-variant | TLE1 | GRCh38.p7 | 9:81593309 | AGAGAAGACAGAAAA[-/C]ACATTTACAGAGGAA | 7088 |
rs773915034 | in-del | -/TTAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629297 | TAATGCAATTTATCC[-/TTAAA]TTAAATTAATTAAAA | 7088 |
rs773917833 | in-del | -/AA | 3.37516e-05 | 0.00410788 | intron-variant | TLE1 | GRCh38.p7 | 9:81616151 | TCAACAAGCATAATC[-/AA]AAGTTTTCGTGATTT | 7088 |
rs773933352 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636872 | GCCAGGTGTGGTGGC[A/G]GATGCCTGTAATCCC | 7088 |
rs773935486 | snp | G/T | 1.75801e-05 | 0.00296475 | missense | TLE1 | GRCh38.p7 | 9:81611923 | AAAGGAGCAGGATAT[G/T]GGCCGGGCACTGCCA | 7088 |
rs773935551 | snp | A/G | 3.2962e-05 | 0.00405954 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590852 | AGCGATGTTGCCGTC[A/G]CTGCAGCATGAGAAG | 7088 |
rs773955191 | snp | A/T | 1.6489e-05 | 0.00287128 | intron-variant | TLE1 | GRCh38.p7 | 9:81633377 | TGTCTGCTCCCGAGG[A/T]TACCAAGAAACGCAC | 7088 |
rs773969751 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604857 | ATTCCTTCCTGCATG[C/T]GCTTCAGCTTCACCC | 7088 |
rs773993344 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667068 | GGTTTGGAGTTTGGA[A/G]TTTTGATTAAGCCAC | 7088 |
rs774004319 | snp | A/G | 3.31785e-05 | 0.00407286 | intron-variant | TLE1 | GRCh38.p7 | 9:81585497 | AGTTTCCTTTCGGCT[A/G]AACTCACCACAGTAA | 7088 |
rs774050056 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621712 | AACCAGCCAGAGGTA[A/G]TCAGCCAGGTGGCCA | 7088 |
rs774064381 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596833 | TGTTCCTTGATCCAA[A/G]GGCTGGTTACACAGG | 7088 |
rs774071634 | snp | A/T | 1.7297e-05 | 0.00294078 | intron-variant | TLE1 | GRCh38.p7 | 9:81616178 | GATTTAGCTTGTAAC[A/T]GACAGACTTTTCCCT | 7088 |
rs774082399 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686096 | GGTGTCCATTCAGCT[A/G]CCATTCTTCTTGGTG | 7088 |
rs774089151 | snp | A/C | 1.6549e-05 | 0.0028765 | intron-variant | TLE1 | GRCh38.p7 | 9:81620561 | GAGGGAATTACTCTG[A/C]AAGACAAAAAAATTA | 7088 |
rs774094033 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654684 | ATGACACATTTATGT[C/T]ATTATTGCAAGTTCA | 7088 |
rs774145270 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653661 | ACAGCTTTCTATTTA[A/G]AAGATATAAAAGACA | 7088 |
rs774161485 | snp | A/T | 1.6636e-05 | 0.00288405 | intron-variant | TLE1 | GRCh38.p7 | 9:81652176 | AAATGAAAGCTGGTT[A/T]TACACACTGTAGGAG | 7088 |
rs774161728 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591632 | GGGGGCCCTCATATG[A/G]TCAACTCCTGAAAGA | 7088 |
rs774174866 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683521 | CACCAGTTTTAATAA[A/G]AATTATGATTACTAG | 7088 |
rs774199139 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665784 | AACTCTATTCATTGG[A/T]TCTCCTTCCTGCAAT | 7088 |
rs774229667 | snp | C/T | 6.59413e-05 | 0.00574163 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616099 | TCCATTTTCCCGGGG[C/T]GAGTGGGCAGGGCTT | 7088 |
rs774238552 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609276 | TTTTAGTAGAGACGG[G/T]GTTTCGCCACATTGG | 7088 |
rs774268057 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669258 | ATCGAAGGCTGTGAG[A/C]ACGCTGCAAATGGCT | 7088 |
rs774317026 | snp | C/G | 5.32363e-05 | 0.005159 | intron-variant | TLE1 | GRCh38.p7 | 9:81634319 | GTTGGTGGTGGTGGT[C/G]AGAGAGAAAAAGGAG | 7088 |
rs774336788 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585229 | CCACCCCTCTTCAGA[A/G]TAGAAACTCATTGTC | 7088 |
rs774386018 | in-del | -/TTGT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662364 | GTGTGCCTGTTTTGT[-/TTGT]GTGTGTGTGTGTGTG | 7088 |
rs774387970 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594732 | TGGCAGCTTTAAATA[C/T]AATGTAAACACCATG | 7088 |
rs774403387 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677424 | CGAAAAATTAGCCGG[A/G]CATCGTGGCAGACGC | 7088 |
rs774432310 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586020 | TCGTTAGGTGACTTT[-/T]TTTTTTTTTTTTTTT | 7088 |
rs774435658 | snp | C/G | 1.64817e-05 | 0.00287064 | missense | TLE1 | GRCh38.p7 | 9:81613500 | TGCTGGATTTCAGAA[C/G]AGGCGTGCTGGCTTT | 7088 |
rs774454556 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637470 | ACTTTTGTGGTTAAA[C/T]CCAACAGTTTGACTA | 7088 |
rs774464334 | snp | C/T | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81691114 | CAAGTATTTATCTTA[C/T]GTTGGAAACTAGTTA | 7088 |
rs774491261 | snp | C/T | 2.12208e-05 | 0.00325729 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587636 | GAGGAAGACACACCC[C/T]AGCCACCTCCCAGAC | 7088 |
rs774518227 | snp | C/T | 7.98053e-05 | 0.00631635 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634199 | GGCCGGCACTGCCCC[C/T]GAGGGGCGGGATTCC | 7088 |
rs774521883 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630288 | CCACAAAAGAGCGAA[C/T]GCAGAGGATGAGAAT | 7088 |
rs774522189 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664398 | GAGGCCTCCTTCAGG[-/A]TATCTGCTACTCAGA | 7088 |
rs774558151 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685673 | AGTTCAACTAAAGCT[C/T]ACCTGTTTGTGCATT | 7088 |
rs774566236 | in-del | -/CA | 4.94609e-05 | 0.00497272 | intron-variant | TLE1 | GRCh38.p7 | 9:81633390 | GGTTACCAAGAAACG[-/CA]CAGACATGCCCGTTC | 7088 |
rs774583011 | snp | A/G | 1.6543e-05 | 0.00287597 | intron-variant | TLE1 | GRCh38.p7 | 9:81654039 | TGGCGATTTCAGTCT[A/G]TAAAGACAAAGCCAC | 7088 |
rs774599116 | snp | A/C/T | 0.000148343 | 0.00861112 | synonymous-codon, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587759 | GTTGTCCAAACCACC[A/C/T]GTCCAGAGCTTGGTG | 7088 |
rs774606207 | snp | C/T | 0.000109932 | 0.0074131 | intron-variant | TLE1 | GRCh38.p7 | 9:81634086 | CTAATCTGGCTTGCC[C/T]GGCCTCTCACCTCTG | 7088 |
rs774610033 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667386 | GAGACAGACTGTCTC[-/AA]AAAAAAAAAAAAAAA | 7088 |
rs774701989 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630850 | ACAAAGTTTGAAGAG[-/C]TACTTAATTTTATGT | 7088 |
rs774762475 | snp | A/G | 3.33962e-05 | 0.0040862 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685727 | TTCATAATACTGTAA[A/G]GAGAAAAAAGAATCA | 7088 |
rs774765349 | snp | C/G | 2.45969e-05 | 0.00350683 | splice-acceptor-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687435 | AGCCTGGTGCGGCGT[C/G]TGGGGGCGACCAGCG | 7088 |
rs774786665 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604455 | GAAGAGCTGCCATGA[A/G]GATGATAGATTAGCA | 7088 |
rs774789533 | snp | C/T | 1.69035e-05 | 0.00290714 | intron-variant | TLE1 | GRCh38.p7 | 9:81613570 | TTTTAATCCAAGCCA[C/T]ATTACACAATTTATC | 7088 |
rs774850764 | snp | A/T | 1.65482e-05 | 0.00287643 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81652187 | GGTTATACACACTGT[A/T]GGAGGTAGACCTGGT | 7088 |
rs774884416 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669253 | GAAAATCGAAGGCTG[-/T]TGAGAACGCTGCAAA | 7088 |
rs774904987 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680735 | TGCTTGCAAAGAACA[A/G]GCCTGGCTAATGAAG | 7088 |
rs774927089 | snp | C/T | | | synonymous-codon | TLE1 | GRCh38.p7 | 9:81590861 | GCCGTCGCTGCAGCA[C/T]GAGAAGCAGACCTTG | 7088 |
rs774930345 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675854 | GACAGGTGCCTGCCA[C/T]CACGCCCAGCTAATT | 7088 |
rs774943409 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640967 | CCAAGAAAAACTATG[A/T]CATAAAAATCACAGA | 7088 |
rs774985217 | snp | C/T | 4.94173e-05 | 0.00497053 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593145 | GATGGTCACAGCGCA[C/T]ACCACCTCCCCGTGG | 7088 |
rs774996377 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640697 | ATTTTACTTAGTGCA[G/T]CTTGGGTCAATTATA | 7088 |
rs775085095 | in-del | -/GGTTTCCCCCCAGGGATTC | 1.7828e-05 | 0.00298558 | splice-acceptor-variant | TLE1 | GRCh38.p7 | 9:81593274 | TGGAAGGAGTATGCA[-/GGTTTCCCCCCAGGGATTC]CTTTTGGAAAAACGA | 7088 |
rs775094836 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630227 | GGTCCCGGAGACCCT[C/T]GCAAATCTATGAGGG | 7088 |
rs775098873 | snp | A/G | 1.77071e-05 | 0.00297544 | intron-variant | TLE1 | GRCh38.p7 | 9:81591094 | ATAATGAATTACCGA[A/G]CAATCATAGCACCAT | 7088 |
rs775136823 | in-del | -/T | 4.96184e-05 | 0.00498063 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685784 | CACTCTGCTAACACG[-/T]TTGCTAATATCATAT | 7088 |
rs775148291 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629086 | CTGTGACATAAAATG[C/G]ATCACTGCAAAATGA | 7088 |
rs775157249 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618987 | CCAACCAGACAAACC[-/T]TAGTACATGCAGGTT | 7088 |
rs775165210 | snp | A/G | | | intron-variant, downstream-variant-500B | TLE1, LOC105376106 | GRCh38.p7 | 9:81590484 | TATCAAGGGCCTTTT[A/G]TGCTGCCGTGTAATC | 7088 |
rs775201493 | snp | A/C | 3.96173e-05 | 0.00445051 | intron-variant | TLE1 | GRCh38.p7 | 9:81610339 | CTCAGTTTATTGCAG[A/C]AGGCACTTTGTGAAC | 7088 |
rs775202869 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652441 | TTATTTTCACAGAAC[A/C]TAGATAGGGAAAGAA | 7088 |
rs775215814 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652813 | ATACCCATTTTAATA[C/T]CTAAAACTTTAATAT | 7088 |
rs775225992 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81664524 | TTAAAATATAATTAT[G/T]CCGATAAAATAACTA | 7088 |
rs775230047 | snp | A/C | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686371 | CTTTGGTTTTTAAAT[A/C]CCTGCCAAAATATGT | 7088 |
rs775260053 | snp | G/T | 1.64958e-05 | 0.00287187 | missense | TLE1 | GRCh38.p7 | 9:81590960 | GGTTGGAGCCGCCAG[G/T]TCCCAAATGGACAAA | 7088 |
rs775265484 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673713 | TGACACGGGGAGGGG[-/G]CGGCTTCTGGCGGAC | 7088 |
rs775281970 | snp | C/G | 1.79358e-05 | 0.00299459 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611940 | GCCGGGCACTGCCAG[C/G]GGTGTCCTCAAGCCA | 7088 |
rs775289856 | snp | C/T | 4.94523e-05 | 0.00497229 | intron-variant | TLE1 | GRCh38.p7 | 9:81616722 | AAAGAAACATTAACG[C/T]CATTTACTAAAAGCT | 7088 |
rs775293272 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599084 | GCCTATGAACAGGAC[C/T]GCTGAGGTGTGAAGT | 7088 |
rs775357002 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639594 | TTTTTTTTTGTTTTT[G/T]TTTTTTTTGAGACAG | 7088 |
rs775358032 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675193 | GATAGATATTACAAA[A/G]TGTTAATTTATAGAC | 7088 |
rs775371794 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81676292 | AAGTCCCTAACTCAG[A/C]TTCAAGCAGACTGCA | 7088 |
rs775392426 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596587 | GAGGAACTAGGAAAA[C/G]TAAAACCAATCAGAA | 7088 |
rs775449128 | snp | A/T | 1.6517e-05 | 0.00287372 | intron-variant | TLE1 | GRCh38.p7 | 9:81616602 | TTTTTCATAACATTA[A/T]TCAAATCATTCTGAA | 7088 |
rs775479085 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606787 | TAATTAAAAAAAAAA[-/C]CATATATATATATAT | 7088 |
rs775507928 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631612 | ACATATATGGTATGC[-/A]CTCAATGAACATAGC | 7088 |
rs775554413 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602555 | TTGACCGCACCTTGT[C/T]ACATGAGGTCAGGTG | 7088 |
rs775567072 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636727 | TAAAGATTTCCGGCC[A/C]GGCACAGTGGCTCAC | 7088 |
rs775579666 | snp | C/T | 1.64787e-05 | 0.00287038 | utr-variant-3-prime | TLE1 | GRCh38.p7 | 9:81584180 | ATTCAACTATAAACG[C/T]TAAACCACATAATGT | 7088 |
rs775600326 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627548 | AACTTTCTCAAAGAA[C/G]AACCATTTTTTTAAG | 7088 |
rs775640074 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684230 | AGATGTTAGCCACAG[A/G]TCTTCTAGCCCATTT | 7088 |
rs775644982 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | TLE1 | GRCh38.p7 | 9:81616070 | TCCTTCTTTAGCAGG[C/T]GATTTTTGTCGATTC | 7088 |
rs775654548 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639839 | TCAGCCCACCTCGGC[C/T]TCCCAAAGTGCTGGG | 7088 |
rs775662773 | snp | A/G | 1.69694e-05 | 0.0029128 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611853 | GTGTAAACTGGCGTA[A/G]GCAGCGCCTGGGCTG | 7088 |
rs775663227 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659679 | CACTGATTTGCATAT[A/G]GTAATACAGTTAGCC | 7088 |
rs775673083 | snp | C/T | 0.000164946 | 0.00907996 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685829 | TCCAATCTTTGATAC[C/T]TACCATCACATAGTG | 7088 |
rs775688432 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644178 | GCTTTGGAAAACAGT[C/T]TGGCTGTTGCTCAAA | 7088 |
rs775736707 | snp | C/T | 3.30327e-05 | 0.0040639 | intron-variant | TLE1 | GRCh38.p7 | 9:81615944 | CCACAATGAAAAATA[C/T]ACTGCCAAACAGGCA | 7088 |
rs775848570 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651243 | TCAAGGCACTCACAT[A/G]TGAATAAAATCAGAA | 7088 |
rs775855832 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678949 | AGTTTGAGACCAGCC[C/T]GGACAACATGCAGAA | 7088 |
rs775866791 | snp | A/G | 2.34475e-05 | 0.00342391 | intron-variant | TLE1 | GRCh38.p7 | 9:81620925 | CTATGAGCAAATCTT[A/G]AGATTACTCTATTAG | 7088 |
rs775868102 | snp | A/G | 1.66935e-05 | 0.00288903 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685913 | TAGGAAAACAAAACA[A/G]GCAACTTAATGTAAA | 7088 |
rs775886203 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614641 | GGGATAATGCCTACC[A/G]GGACCAGGTAAGGAT | 7088 |
rs775913135 | snp | A/G | | | upstream-variant-2KB, intron-variant | TLE1, LOC101927502 | GRCh38.p7 | 9:81690174 | CAAAGACTAGCTGCG[A/G]AGTTTCTTATTGGAG | 7088 |
rs775921058 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671506 | AAAAATTAGCAGGGC[A/G]TGGTGGCATGTGCCT | 7088 |
rs775939503 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585143 | TCGACTTCTCTAACC[C/G]TGGATTCCTCATCAT | 7088 |
rs775948803 | snp | C/T | 3.29674e-05 | 0.00405988 | intron-variant | TLE1 | GRCh38.p7 | 9:81616726 | AAACATTAACGCCAT[C/T]TACTAAAAGCTAAGA | 7088 |
rs775960125 | in-del | -/AAAAAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655853 | GCAAGACCCTGTCTC[-/AAAAAA]AAAAAAAAAAAGAAA | 7088 |
rs775980054 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650446 | ATATGTTTTCTTTTA[A/G]TCAAAACAGGCTTTT | 7088 |
rs775993111 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | TLE1 | GRCh38.p7 | 9:81583721 | GTAATAAACCAAATA[C/T]ATTTACAATTTATAC | 7088 |
rs776027452 | snp | C/T | 1.66258e-05 | 0.00288316 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685766 | ATTAACTCATGTTTT[C/T]TACACTCTGCTAACA | 7088 |
rs776058253 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628960 | CATGAATGCCACTGC[A/G]TAGGTCTATACACCG | 7088 |
rs776063768 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598172 | GCTCTTCAAGCTCTT[C/T]AGGGCTCATGAAGCC | 7088 |
rs776097691 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622320 | AATGGGGCACAGAGG[A/C]TGGGTGTGCTGACCA | 7088 |
rs776122246 | snp | A/C | 1.66056e-05 | 0.00288141 | intron-variant | TLE1 | GRCh38.p7 | 9:81584548 | AGCAAAGGAATATCT[A/C]GTTTTCACAAGGTTA | 7088 |
rs776126837 | snp | C/T | 0.000115303 | 0.00759199 | missense | TLE1 | GRCh38.p7 | 9:81593111 | TCCCGCCTGTGTACA[C/T]GTGTCTCGTGGGGTT | 7088 |
rs776149401 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597500 | AACAAACGCCCAAAG[A/C]GTAGAGATGGACGTT | 7088 |
rs776181891 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660261 | TGAACCAAAACTTAA[A/T]CTCCATGCACCCCTA | 7088 |
rs776229783 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655626 | GCCCATCCTTGACCT[G/T]ACTTATTTCATCATT | 7088 |
rs776315726 | snp | C/G | 4.95782e-05 | 0.00497862 | intron-variant | TLE1 | GRCh38.p7 | 9:81652293 | TGTTGTTGATGCTTT[C/G]AAAACAAGGAGAAGA | 7088 |
rs776318139 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637956 | TGAGGGCTACAAACC[-/T]TTTGTTTCCTAGGAC | 7088 |
rs776326611 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81584204 | ATAATGTTTTCAGTA[A/G]ATGACTTCATAGACT | 7088 |
rs776383012 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674972 | CCATCCTGGACAACA[C/T]AGTGAGACCTCATCT | 7088 |
rs776413310 | snp | A/G | 1.78061e-05 | 0.00298375 | intron-variant | TLE1 | GRCh38.p7 | 9:81591102 | TTACCGAGCAATCAT[A/G]GCACCATGTTCTCTA | 7088 |
rs776418497 | snp | A/C | 3.57507e-05 | 0.00422777 | intron-variant | TLE1 | GRCh38.p7 | 9:81634322 | GGTGGTGGTGGTGAG[A/C]GAGAAAAAGGAGGAG | 7088 |
rs776425096 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81608975 | AGAAAGAAAAAGAAA[A/G]AGAAAAAAAAGCAAC | 7088 |
rs776434363 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685802 | GCTAATATCATATGA[A/G]AAAGGAAAAAGTCCA | 7088 |
rs776436394 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674061 | AATGGCACAAATAAC[A/G]GTGGCTGCATTTTGT | 7088 |
rs776472802 | in-del | -/T | 2.55079e-05 | 0.00357118 | intron-variant | TLE1 | GRCh38.p7 | 9:81620956 | CATATTCTTTAACTG[-/T]TAAGAGTCAATGTGT | 7088 |
rs776473626 | in-del | -/CAGCAGGCGTT | 0.000174 | 0.00932577 | intron-variant | TLE1 | GRCh38.p7 | 9:81633326 | GTGTGTGTGTGTGTG[-/CAGCAGGCGTT]TGAGTACTTACTGTG | 7088 |
rs776491387 | snp | A/G | 2.62333e-05 | 0.0036216 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687448 | GTCTGGGGGCGACCA[A/G]CGAGGGGGACCGAGG | 7088 |
rs776496432 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666227 | GAGAAAGAAATCTTT[C/T]TCCAAACTCCGCAGA | 7088 |
rs776499444 | snp | A/G | 1.66807e-05 | 0.00288792 | intron-variant | TLE1 | GRCh38.p7 | 9:81611725 | CGCTCAATGGAGCAT[A/G]CAGCGTTCCTACCCC | 7088 |
rs776505338 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631764 | TTCTGTGATTTCATC[C/T]AGGGTTAGGTTTTTA | 7088 |
rs776558164 | snp | A/T | 2.77913e-05 | 0.00372758 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634110 | ACCTCTGTGGTGCTC[A/T]GCATCGTGGTGCTTC | 7088 |
rs776581986 | in-del | -/AATC | 3.33745e-05 | 0.00408487 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685738 | GTAAAGAGAAAAAAG[-/AATC]AAGCATTTCATTAAC | 7088 |
rs776640069 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673825 | ATAAACCCAAAAAGC[C/T]GACTTCTGAAAGCCA | 7088 |
rs776699132 | snp | C/T | 1.65075e-05 | 0.00287289 | missense | TLE1 | GRCh38.p7 | 9:81620460 | TGGCTGGAGTCCTTA[C/T]CATCCACCTTCCTTT | 7088 |
rs776739183 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644862 | AGCCAGGCATGGTGG[A/T]GTGTGCCTGTAATCC | 7088 |
rs776747849 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656289 | TTGCAACAGGGTTCT[A/G]CACTGTCTATTTGAG | 7088 |
rs776753120 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81626320 | ATTAACTTCTCGGTG[A/G]ACATTAAAACAATTA | 7088 |
rs776754863 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601800 | ACTACTTAATAATTC[A/G]AAAATGCGAACAAGG | 7088 |
rs776755520 | snp | A/C/T | 4.94387e-05 | 0.00497165 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616084 | GCGATTTTTGTCGAT[A/C/T]CCATTTTCCCGGGGC | 7088 |
rs776782637 | snp | A/G | 1.9877e-05 | 0.00315247 | intron-variant | TLE1 | GRCh38.p7 | 9:81610177 | AATACCAATGACTGA[A/G]TAACCACCTTTAAAA | 7088 |
rs776786278 | snp | C/T | 1.64993e-05 | 0.00287218 | missense | TLE1 | GRCh38.p7 | 9:81585561 | AGGTGCAGCTGGTAC[C/T]TGTCAGGCTTGTTCA | 7088 |
rs776814714 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657667 | ATACAGTGGTCTCTC[-/G]GTATCTGTGAGGGAT | 7088 |
rs776820687 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649758 | TTCCCGGTACCTCCT[A/C]CCCTCTGGGGAGACA | 7088 |
rs776834439 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681328 | GCCGAGGCGGGGGGA[A/T]TCACTTGAGGTCAGG | 7088 |
rs776839824 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677681 | CTACTTAGATCAGTC[A/G]TGGTGCTAATACCAA | 7088 |
rs776872118 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659487 | TGCATTCAAGAGCTA[A/T]CCACAAACCAAATCT | 7088 |
rs776874763 | snp | C/G | 5.59801e-05 | 0.00529026 | intron-variant | TLE1 | GRCh38.p7 | 9:81600106 | AATGTGCTGGGGCAG[C/G]AACAAGGCTCCTAAA | 7088 |
rs776876992 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683150 | AAGGTGGGAAGGGAG[A/G]GCGGTCGTCACACTG | 7088 |
rs776878009 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653545 | CCACCCCTTCAAGGA[C/G]AGCATTAAGACAACT | 7088 |
rs776940779 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612055 | TTAGTGTCACTCATG[A/G]GGAGAGAGAAAGAGG | 7088 |
rs776992588 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81648794 | ATTTTGTTTTGATCA[G/T]TCTTAATAGAAATTT | 7088 |
rs777002641 | snp | A/G | 9.14503e-05 | 0.00676142 | intron-variant | TLE1 | GRCh38.p7 | 9:81611962 | CTCAAGCCAGCTGCT[A/G]AAAGGAAACACAAGC | 7088 |
rs777050238 | snp | G/T | 0.000114066 | 0.00755117 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687320 | CCACTCGCATGGCGC[G/T]GCCGGACACGCACCT | 7088 |
rs777135478 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592283 | GAACGGCGTAAACCC[C/T]GGAGGCGGAGCCTGC | 7088 |
rs777135752 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679308 | ATTTTTCTTCACTTT[-/T]TTTTCTTTTTTTTTC | 7088 |
rs777153284 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679501 | TCAAACCACACCTCA[C/T]GGGGAAAAAAAATCA | 7088 |
rs777164289 | snp | C/T | 7.38089e-05 | 0.00607446 | intron-variant | TLE1 | GRCh38.p7 | 9:81620946 | ACTCTATTAGACATA[C/T]TCTTTAACTGTAAGA | 7088 |
rs777171950 | in-del | -/TG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662362 | TTAGTGTGCCTGTTT[-/TG]TGTGTGTGTGTGTGT | 7088 |
rs777189645 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607906 | GCTACTGATTCCTAG[C/T]GTAGACAAAAACCTC | 7088 |
rs777213112 | snp | A/G | 1.74756e-05 | 0.00295593 | intron-variant | TLE1 | GRCh38.p7 | 9:81600126 | AGGCTCCTAAACAGG[A/G]CAAAGATACAAATGG | 7088 |
rs777213252 | snp | A/C/T | 8.31959e-05 | 0.00644918 | intron-variant | TLE1 | GRCh38.p7 | 9:81585492 | CCTCCAGTTTCCTTT[A/C/T]GGCTGAACTCACCAC | 7088 |
rs777259738 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658842 | AGGGTATTCTGGTAA[C/G]ATTCTTAATTTAGCA | 7088 |
rs777267080 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597231 | CAGCACTTGACACCT[A/G]CAGTGAGTCTTCAGG | 7088 |
rs777336894 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672702 | GTAACCAAGCAACAA[C/T]TTGACCCTCTAATTC | 7088 |
rs777351562 | snp | A/G | 3.29489e-05 | 0.00405874 | missense | TLE1 | GRCh38.p7 | 9:81616031 | CTTGCCGAGGAGGCC[A/G]TGGAAGCTGGACTGC | 7088 |
rs777355067 | in-del | -/TGTGTCATCCCGCC/TGTGTGTCATCCCGCC | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587920 | CCGTGTGTGTGTGTG[lengthTooLong]TGTGTGTGTGTGTGT | 7088 |
rs777366888 | in-del | -/AAAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653025 | CCCAACTCCACCCAC[-/AAAT]AAAAACAAAGCCATA | 7088 |
rs777368754 | snp | G/T | 1.74756e-05 | 0.00295593 | intron-variant | TLE1 | GRCh38.p7 | 9:81600049 | AGATTCTGAGTTCTA[G/T]GACCTAACTTCCTCT | 7088 |
rs777375992 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81678542 | TTAGGGGCTGGGAGC[A/C]GTGGCTCACGCCTGT | 7088 |
rs777382048 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601966 | TGGGGAGGAAGCAGA[C/T]AGAAACACGGCTTGT | 7088 |
rs777395152 | snp | A/G | 1.64852e-05 | 0.00287094 | missense | TLE1 | GRCh38.p7 | 9:81590941 | GCTCCGCCTTGATGC[A/G]CGGGGTTGGAGCCGC | 7088 |
rs777429903 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681065 | CCACTAAAGAACAAC[A/G]CATTTTTCTAAGAGA | 7088 |
rs777439492 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81659422 | TAATGCTTATAAACT[C/T]TCCCTGTGCCTAGAT | 7088 |
rs777496337 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622634 | AATTTCCGCTTGAGC[A/G]GCTTAAATGAAGCTT | 7088 |
rs777527591 | snp | G/T | 2.56289e-05 | 0.00357963 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688290 | AACTCAATTCTCCGG[G/T]CAATTTCCAACTTTA | 7088 |
rs777539773 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591296 | CACAGAGCTGAAACT[A/G]TCTAGGTATGAGGTA | 7088 |
rs777546185 | snp | A/C | 8.62195e-05 | 0.00656524 | missense | TLE1 | GRCh38.p7 | 9:81611900 | TGCCAGCGTGGGGGA[A/C]CATCCCAAAAGGAGC | 7088 |
rs777592663 | snp | A/G | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589989 | TGACTTCTGGAGCCC[A/G]TCCCTTCTCTGTGCA | 7088 |
rs777596511 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633114 | GCCTCCAAATTATGC[C/T]TCTCTTGTCTGATGC | 7088 |
rs777633381 | in-del | -/AATT | 3.39662e-05 | 0.00412092 | intron-variant | TLE1 | GRCh38.p7 | 9:81652151 | CACGTAAAGCCATCA[-/AATT]AATAAGAAATGAAAG | 7088 |
rs777644066 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81598581 | CCTAATCACTTATAT[A/G]TTGAGGAAAAGTTGC | 7088 |
rs777666987 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665363 | AGTCACCAATTACTG[A/G]CAGATAATAACTTTT | 7088 |
rs777667849 | snp | A/G | 1.87002e-05 | 0.00305773 | intron-variant | TLE1 | GRCh38.p7 | 9:81611994 | GCACATCATTCAACT[A/G]ACCCACTCCATCAAA | 7088 |
rs777670614 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662121 | AAAGAGAAAAAAACA[C/G]GTAAAGATGTAACAG | 7088 |
rs777672634 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639836 | TGATCAGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 7088 |
rs777679035 | snp | A/G | 1.65842e-05 | 0.00287955 | intron-variant | TLE1 | GRCh38.p7 | 9:81611762 | AGCCCACCCGACAGC[A/G]GCCTACCATGGGGGA | 7088 |
rs777688732 | snp | A/G | 1.65075e-05 | 0.00287289 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81585593 | GTGCAGCACCTCCAC[A/G]TTGCTGCTCTCCATG | 7088 |
rs777691193 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641699 | CAATATCATTAATCA[C/T]GAAGGAAACGCAAAT | 7088 |
rs777703293 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597922 | ACCAGGCTCCTGTTA[A/G]TAAAACTATGCTGTG | 7088 |
rs777709580 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651681 | ATGATAATTCAGAGA[A/C]CCATTTTGACCTCAC | 7088 |
rs777732679 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628891 | CTGAGAATTTGATGA[A/G]TTATAGTCTCTCCCC | 7088 |
rs777784050 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639444 | CATGACAGGAAGGAT[A/G]AGGAAATTTATTCTT | 7088 |
rs777829206 | snp | A/T | 1.90616e-05 | 0.00308714 | intron-variant | TLE1 | GRCh38.p7 | 9:81633312 | GTGTGTGTGTGTGTG[A/T]GTGTGTGTGTGTGCA | 7088 |
rs777909727 | in-del | -/AAAAC | 1.65696e-05 | 0.00287828 | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587834 | CTGGAATTGCCTGAT[-/AAAAC]AAACCAGATTGAATA | 7088 |
rs777914777 | in-del | -/GCGGCGGCT | 0.00140133 | 0.0264329 | cds-indel | TLE1 | GRCh38.p7 | 9:81611802 | GCCACCACGGCGGCC[-/GCGGCGGCT]GCGGCGGCTGCGGCG | 7088 |
rs777917412 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680032 | ATAAACACTATTTGG[A/G]AGAACATCTTAAGTC | 7088 |
rs777921484 | snp | A/G | 2.25751e-05 | 0.00335962 | intron-variant | TLE1 | GRCh38.p7 | 9:81620903 | CCTGGTCAGGAATAC[A/G]AATGGCCTATGAGCA | 7088 |
rs777951267 | snp | A/G | 0.00014949 | 0.00864424 | missense | TLE1 | GRCh38.p7 | 9:81620443 | TTTAATTACTTACAT[A/G]GTGGCTGGAGTCCTT | 7088 |
rs777963929 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684690 | CATCAAGTAAGAATT[A/G]TATTGTTGCACTTTG | 7088 |
rs777986794 | snp | A/G | 2.35835e-05 | 0.00343383 | stop-gained, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687425 | GCTGGCCTGCAGCCT[A/G]GTGCGGCGTCTGGGG | 7088 |
rs777991146 | snp | A/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588345 | ACAGCAATGCCCTAC[A/G]TGCCAACAGAGCATG | 7088 |
rs777997847 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687704 | AGGCCAAAGGGAAGG[A/G]GGCTCCCCGGCGGCC | 7088 |
rs778037420 | snp | A/G | 1.65375e-05 | 0.0028755 | intron-variant | TLE1 | GRCh38.p7 | 9:81653944 | AGAAGCAACATAATT[A/G]CACTTTAACAGCTGA | 7088 |
rs778057049 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634708 | GCATGTCACTCAATC[A/T]AAGATGCCACAGATT | 7088 |
rs778128591 | snp | C/G | 0.000100849 | 0.0071003 | intron-variant | TLE1 | GRCh38.p7 | 9:81613562 | AGTATTATTTTTAAT[C/G]CAAGCCATATTACAC | 7088 |
rs778147575 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602268 | CCGGAAAAGCAGGCT[C/G]GGGGGATATTACCAG | 7088 |
rs778152126 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627016 | GCTCAGCTGTTTCTG[C/T]GCCTCTTTGCTCTCC | 7088 |
rs778162952 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672307 | CCAATGGCTCTGCCT[C/T]TCTCCCCTGCAATAA | 7088 |
rs778172740 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646026 | AGTAAAAATCACAGG[A/C]AACTATGTGGGTGGG | 7088 |
rs778185627 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592695 | CGAGTGGATGGCAGG[C/G]ATCAGAGTCCAGGCC | 7088 |
rs778200754 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81614400 | GGACCCACCAGTGCA[C/G]ATCAGAGACTGAACA | 7088 |
rs778224787 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643882 | CACATAGGCCAACTC[C/T]TCCTGCATGACCACT | 7088 |
rs778225568 | snp | C/G | | | intron-variant, nc-transcript-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589663 | TTCCTCTATAAAATG[C/G]GGCAAATAGCAGGAC | 7088 |
rs778313175 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591268 | TTAGGTAACTGCTTC[C/T]GGTGTCCTGCATCAC | 7088 |
rs778331035 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623536 | GTAATCCCAGCACTT[A/G]GGGAGGCCGAGGCAG | 7088 |
rs778338568 | in-del | -/AAA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645010 | TGTCTCAAAAAAAAA[-/AAA]AAAAAAAAAAAGGTG | 7088 |
rs778338864 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655192 | AAGATGGTGAAACCC[C/T]GTCTCTACTCAAAAT | 7088 |
rs778344305 | snp | C/T | | | synonymous-codon | TLE1 | GRCh38.p7 | 9:81620528 | TTTATCTGTGCCTCT[C/T]AGACTGTCTGGGACC | 7088 |
rs778371456 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671109 | GGAGGCAATGACTGC[A/G]GTGAACTGAGATCAC | 7088 |
rs778393484 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81602119 | CAAGTGGGCTTTGAA[C/G]GACAGAAAATACTTC | 7088 |
rs778399500 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632043 | TGCAGTGAGCCGAGA[C/T]AGTGCTACTGCACCC | 7088 |
rs778419256 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642926 | AAATCCTACCACTTA[C/T]GACAACATGGGCAGA | 7088 |
rs778422903 | snp | A/G/T | 0.000436223 | 0.0147623 | intron-variant | TLE1 | GRCh38.p7 | 9:81633331 | TGTGTGTGTGCAGCA[A/G/T]GCGTTTGAGTACTTA | 7088 |
rs778436026 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680881 | GATGTTGACTTAGGG[A/G]GAAAAAAAATCTCAA | 7088 |
rs778442298 | snp | A/G/T | 3.37275e-05 | 0.00410644 | intron-variant | TLE1 | GRCh38.p7 | 9:81585682 | AAGACAGGCTCACTC[A/G/T]TTATTCCGCCTGATA | 7088 |
rs778442577 | snp | A/C | 5.9625e-05 | 0.00545976 | intron-variant | TLE1 | GRCh38.p7 | 9:81600135 | AACAGGACAAAGATA[A/C]AAATGGAGAAATTCT | 7088 |
rs778462154 | snp | A/G | 0.000130984 | 0.00809166 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687473 | CCGAGGGACGGGAAT[A/G]CGGGCGGATGAATAA | 7088 |
rs778469722 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617135 | TTACTAGTTAATGCA[-/AA]AAAAAAAAAAAAAAA | 7088 |
rs778473115 | snp | G/T | 3.2993e-05 | 0.00406145 | synonymous-codon, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685847 | CCATCACATAGTGCC[G/T]CTGCATTTCTGTCTT | 7088 |
rs778477247 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683919 | CATGATAAAGAAGAG[A/G]TCATCCCGCCACATA | 7088 |
rs778512340 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639373 | GCTGGCCTGCATCTG[C/T]ACTCTCTAACCAAAA | 7088 |
rs778516505 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654141 | TCTCCCTTGCTCTGG[-/A]AATGTGTATAAAATG | 7088 |
rs778517203 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625965 | GCTGCCCTGTCAATG[A/C]TATCAAACACTAGTT | 7088 |
rs778520235 | snp | G/T | 1.64942e-05 | 0.00287173 | utr-variant-3-prime | TLE1 | GRCh38.p7 | 9:81584157 | TAAATTCGAAACATT[G/T]TGGCCCAATTCAACT | 7088 |
rs778524240 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639132 | GGTCTCACCATGTTG[C/T]CCAGGCTGGTCTGGA | 7088 |
rs778526127 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658419 | TATGTCCTGGAAATT[C/G]TACATAAATGGTCTG | 7088 |
rs778529809 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81672083 | CCACTTCTCAAGCTA[A/G]GCAGAAAGAGCCATG | 7088 |
rs778531548 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81687885 | GCATTGACATGTAAA[C/T]AGGCGAGAGGAGAAA | 7088 |
rs778539360 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633001 | TTAAACTACAGTCAA[C/T]CAGACTTAGAATGCA | 7088 |
rs778560950 | snp | C/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589433 | TACATGGCCCTATTA[C/G]ATGCAGCAGCCACTA | 7088 |
rs778575921 | in-del | -/TGTGTGT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633310 | GTGTGTGTGTGTGTG[-/TGTGTGT]GTGTGTGTGCAGCAG | 7088 |
rs778583103 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670896 | AGGATGGGCTGGGTG[C/T]CGTGGCTCATGCTGT | 7088 |
rs778619863 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81652251 | GCCATGGTCACCTGT[C/T]TGGCACGTTCAACAG | 7088 |
rs778645331 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601244 | AAGGGGGAAGCCCCC[A/G]GCCACTGAAACTTTT | 7088 |
rs778708461 | snp | A/G | | | | | GRCh38.p7 | 9:81650319 | GGGCGGTGCCTTTGA[A/G]AATTTAAACGTCAGA | 7088 |
rs778724173 | snp | C/T | | | | | GRCh38.p7 | 9:81597842 | CCCACCGGGCTCCTT[C/T]GCAGCTGTGGTGAAC | 7088 |
rs778727545 | snp | A/G | | | | | GRCh38.p7 | 9:81642803 | TGCAGTGCTATTCAC[A/G]AGAGCCAAGATACCG | 7088 |
rs778799449 | snp | A/G | 1.64781e-05 | 0.00287033 | missense | TLE1 | GRCh38.p7 | 9:81593062 | GGGCTCTTATTGCCA[A/G]GGTGGCTGATGTCCC | 7088 |
rs778808759 | snp | A/C | 1.7033e-05 | 0.00291826 | intron-variant | TLE1 | GRCh38.p7 | 9:81590778 | CTAAAGAAGCGAACC[A/C]CTCCTTAGACGACCA | 7088 |
rs778822606 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675998 | GCCACCACACCAGGC[C/T]GACCCACACTAGTTT | 7088 |
rs778843233 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81596288 | CTGTGAACACTCATC[C/T]GTCCCACGGGAAGCC | 7088 |
rs778880629 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81638555 | GCTACTTGAATATAT[C/T]TTAGGAAAAAGTGAT | 7088 |
rs778885941 | in-del | -/CC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606787 | TAATTAAAAAAAAAA[-/CC]ATATATATATATATA | 7088 |
rs778894614 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683542 | TGATTACTAGCTGCA[-/C]CAAATGCCTCCTCAG | 7088 |
rs778901001 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657538 | AGACTTGAACATGGT[C/T]GGAGGACAGTTAAGA | 7088 |
rs778909906 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627428 | TCCACCTGACTTATT[A/G]CATCCACAGTAAACA | 7088 |
rs778979755 | snp | A/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686593 | GACAAAAGCAAAAAA[A/T]GTCAATACAGTTATT | 7088 |
rs778990449 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651316 | AAGGGGACGAACACA[C/T]GAGAACCATCCCAGG | 7088 |
rs779003080 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632263 | AGAGAAATTTATAGG[A/G]CAAGAATTTTAAAAC | 7088 |
rs779050395 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674833 | AGGAGGAAAACCCTA[C/T]AAAAACAGGTGAAGA | 7088 |
rs779054670 | snp | A/C | 1.66685e-05 | 0.00288686 | intron-variant | TLE1 | GRCh38.p7 | 9:81613334 | CAAATCAAGCTGGGA[A/C]TGGGAGAAACCAAAC | 7088 |
rs779077645 | snp | C/T | 1.86027e-05 | 0.00304976 | missense | TLE1 | GRCh38.p7 | 9:81611813 | CGGCCGCGGCGGCTG[C/T]GGCGCTCATCTGGGG | 7088 |
rs779079216 | snp | A/G | 2.02157e-05 | 0.00317922 | missense, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688234 | GGTGCCGGCTCTGCG[A/G]GAACATCGCTCTGGC | 7088 |
rs779108982 | snp | C/G | 1.66167e-05 | 0.00288237 | missense | TLE1 | GRCh38.p7 | 9:81616130 | GCTCGCGGAGAAGAA[C/G]GGTCCTCAACAAGCA | 7088 |
rs779161927 | snp | C/T | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685789 | TGCTAACACGTTTGC[C/T]AATATCATATGAAAA | 7088 |
rs779166170 | snp | C/T | 4.94466e-05 | 0.00497201 | missense | TLE1 | GRCh38.p7 | 9:81620526 | CGTTTATCTGTGCCT[C/T]TTAGACTGTCTGGGA | 7088 |
rs779166237 | snp | A/G | 2.54088e-05 | 0.00356423 | missense | TLE1 | GRCh38.p7 | 9:81611780 | CTACCATGGGGGAGC[A/G]CCCGTAGGCCACCAC | 7088 |
rs779167283 | snp | A/G | 0.000311219 | 0.0124705 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687479 | GACGGGAATGCGGGC[A/G]GATGAATAAAGCAGT | 7088 |
rs779187948 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81646381 | CTAGAGTGTTGGAAT[G/T]TAAGTAGAGAGTACG | 7088 |
rs779230750 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604637 | ACGCACGGTCAGAGG[C/T]ACACTGTCACTGCAC | 7088 |
rs779252862 | in-del | -/C | 6.66089e-05 | 0.00577062 | intron-variant | TLE1 | GRCh38.p7 | 9:81585487 | AACGGCCTCCAGTTT[-/C]CTTTCGGCTGAACTC | 7088 |
rs779283267 | snp | A/G | 0.000200614 | 0.0100133 | synonymous-codon, intron-variant | TLE1 | GRCh38.p7 | 9:81634200 | GCCGGCACTGCCCCC[A/G]AGGGGCGGGATTCCA | 7088 |
rs779294513 | snp | C/T | 0.000125534 | 0.00792155 | intron-variant | TLE1 | GRCh38.p7 | 9:81600057 | AGTTCTAGGACCTAA[C/T]TTCCTCTATCAATTA | 7088 |
rs779351170 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641609 | ATCCTAATTTAAAAA[C/T]GGGCAAAGGACCTCC | 7088 |
rs779351227 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654047 | TCAGTCTATAAAGAC[A/G]AAGCCACACAAATGT | 7088 |
rs779353223 | in-del | -/GCC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673712 | TGACACGGGGAGGGG[-/GCC]GCGGCTTCTGGCGGA | 7088 |
rs779385502 | snp | A/C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81621313 | TATTTTGGGGTCACA[A/C/T]GACATGATCTGACAT | 7088 |
rs779386516 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667984 | GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA | 7088 |
rs779404754 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612788 | GAAGGCTGGGCAAGG[C/T]AGCTCACGCCTGTAA | 7088 |
rs779407462 | snp | C/T | 5.81773e-05 | 0.00539308 | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81587663 | AGACTCCAGGGCAGG[C/T]GGAAGCCACTCAGTC | 7088 |
rs779425431 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81624303 | ATGAACTAGGAATAG[C/T]CCCAAATTCCTGCCT | 7088 |
rs779468911 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644688 | AAAAACCACAGAAGT[C/G]TATGCTTTAAAAAAG | 7088 |
rs779525162 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81612605 | CCCTAGCAGAAAACC[A/T]GCAAACTATAGTCTG | 7088 |
rs779544363 | snp | A/G | 0.0194737 | 0.0967349 | intron-variant | TLE1 | GRCh38.p7 | 9:81652139 | CACACACACACACAC[A/G]TAAAGCCATCAAATT | 7088 |
rs779545373 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641471 | AGGCCCCATCTCAAT[A/G]CAGGAGCACACAGAA | 7088 |
rs779546298 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81653378 | GCAAAGCTAAAATAC[A/C]ATAGTCTTGAGTCAG | 7088 |
rs779565418 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670780 | CTTGGATAAAATAAT[A/G]ACCCAAACAATGGCT | 7088 |
rs779577614 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | TLE1 | GRCh38.p7 | 9:81613454 | GTGGCGCTGGTGCCC[A/G]GCGTTGGCATGTCGC | 7088 |
rs779580160 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644409 | CTAAAATACTGGTGA[C/T]ACGACAACATGGATA | 7088 |
rs779588302 | snp | C/T | 1.69467e-05 | 0.00291085 | intron-variant | TLE1 | GRCh38.p7 | 9:81585686 | CAGGCTCACTCATTA[C/T]TCCGCCTGATACACT | 7088 |
rs779634427 | snp | C/G/T | 0.000106424 | 0.00729403 | missense, intron-variant | TLE1 | GRCh38.p7 | 9:81634259 | TAAGGGGAACTGGGG[C/G/T]TCCGTGGCCATGAGA | 7088 |
rs779656188 | in-del | -/AGGGG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683877 | CACACCATGGTGCTT[-/AGGGG]CTGACCCACTTCACC | 7088 |
rs779660859 | snp | A/C | 1.64887e-05 | 0.00287125 | intron-variant | TLE1 | GRCh38.p7 | 9:81633412 | ATGCCCGTTCAGACA[A/C]AGAGGCAAGAACAGA | 7088 |
rs779662862 | in-del | -/GT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629642 | TGCAAATATCGAATA[-/GT]GTGTTTACACAAACC | 7088 |
rs779674790 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677350 | GTGGGCAGATCATGA[A/G]GTCAGGAGATCGAGA | 7088 |
rs779693110 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81649960 | TGAAAAGAGCCTTCG[A/G]ACATAAATTCATATA | 7088 |
rs779726878 | in-del | -/ACAC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660935 | CCCCATCCCTACTAA[-/ACAC]ACACACACACACACA | 7088 |
rs779738288 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681752 | GTAGTTTTATCTACC[C/T]ATGGCCTGTGACCCT | 7088 |
rs779740096 | snp | A/T | 3.2987e-05 | 0.00406108 | synonymous-codon, intron-variant, utr-variant-5-prime | TLE1 | GRCh38.p7 | 9:81653989 | TTCCTGAGACAGAAA[A/T]GGGATGACTTGTGCA | 7088 |
rs779751393 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81601041 | TGAGCCAATCCCTCC[A/C]AATAACTCCTTCTCC | 7088 |
rs779752447 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607501 | CTGAACACACGCCCC[A/G]TACCTCTAACTCTTG | 7088 |
rs779758866 | snp | G/T | 0.00471202 | 0.0483095 | missense | TLE1 | GRCh38.p7 | 9:81620454 | ACATAGTGGCTGGAG[G/T]CCTTATCATCCACCT | 7088 |
rs779764721 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81657111 | GTTAAACATCTTTTC[A/G]TGTATTTATTGCTCC | 7088 |
rs779806419 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599952 | AAATGGATATGTAAA[A/C]GAAGATTACAAGCAA | 7088 |
rs779825870 | snp | G/T | 1.64735e-05 | 0.00286993 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81593193 | GCGAGCATGCCGGGG[G/T]ATTCCGGGTCCGATG | 7088 |
rs779835433 | snp | A/C | 1.70758e-05 | 0.00292192 | intron-variant | TLE1 | GRCh38.p7 | 9:81685646 | ATGAACTGATGTCTC[A/C]TTTCAGCTTGAAGTT | 7088 |
rs779841223 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81665953 | TCCCCCTTCAGTTCC[A/G]TCTAATTAATGACTT | 7088 |
rs779913750 | snp | A/G | 3.33161e-05 | 0.00408129 | intron-variant | TLE1 | GRCh38.p7 | 9:81613547 | TAAACAAATTAAATG[A/G]GTATTATTTTTAATC | 7088 |
rs779918321 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81620388 | GAATATACTTGGATA[A/C]TCAGGTGAGCAGTAA | 7088 |
rs779938185 | snp | C/G | 0.0108636 | 0.0728957 | intron-variant | TLE1 | GRCh38.p7 | 9:81652144 | ACACACACACGTAAA[C/G]CCATCAAATTAATAA | 7088 |
rs779939783 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584584 | CCTACTATACAATTA[C/G]CAACTTGGACTTAAT | 7088 |
rs779941423 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81637322 | GAGATCGTGCCACTG[C/T]ACTCCAGCCTGGGTG | 7088 |
rs779947714 | snp | G/T | 1.65056e-05 | 0.00287272 | intron-variant | TLE1 | GRCh38.p7 | 9:81584418 | ACACTGTGGTCAAAC[G/T]GTGGATCTAGGTGAG | 7088 |
rs779956899 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81685723 | ACATTTCATAATACT[A/G]TAAAGAGAAAAAAGA | 7088 |
rs779973412 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632020 | GCTTGAACCCAGGAG[A/G]CGGAGGTTGCAGTGA | 7088 |
rs780013289 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622748 | GAAAATGGGCCCCAT[G/T]CAACAGCAGACTTCA | 7088 |
rs780026053 | snp | C/T | 1.66418e-05 | 0.00288455 | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688286 | CGGCAACTCAATTCT[C/T]CGGTCAATTTCCAAC | 7088 |
rs780053545 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644926 | TTGAACCCGGGAAGC[A/G]GAGGTTGCAGTGAGC | 7088 |
rs780061623 | snp | A/G | 3.32546e-05 | 0.00407752 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81591014 | GAGAGTGCAGCCATC[A/G]GGTAGCAATTTACAG | 7088 |
rs780090020 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658291 | GCAGAACCCACAGAT[A/G]CAAAGGGCCGACTGT | 7088 |
rs780134069 | snp | A/G | 1.64817e-05 | 0.00287064 | intron-variant | TLE1 | GRCh38.p7 | 9:81584312 | CTCTTTGGACTGGAA[A/G]AGAAAACAATGGACA | 7088 |
rs780160966 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650757 | GAAGAGGAGGGAGAA[C/T]TGTTTATGCAGAGCT | 7088 |
rs780194427 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684840 | ACTTACACCCTGCCA[C/T]TAATGCTTTCTTTGG | 7088 |
rs780219889 | snp | A/G | 1.64841e-05 | 0.00287085 | missense | TLE1 | GRCh38.p7 | 9:81590931 | GAGGACGTCAGCTCC[A/G]CCTTGATGCGCGGGG | 7088 |
rs780240088 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673724 | GGGGGCGGCTTCTGG[C/T]GGACCAATTCCTAGG | 7088 |
rs780249346 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603729 | ATACAAGGTCAGGCG[C/T]GGTGGCTCATGCCTG | 7088 |
rs780267327 | in-del | -/AAATAAATAAATAAAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666777 | AAGACTCGTCTCACA[-/AAATAAATAAATAAAT]AAATAAATAAATAAA | 7088 |
rs780323074 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656069 | TTGGACAAAATGTAC[C/T]AGAAGGGGAAATGAC | 7088 |
rs780342214 | snp | G/T | 3.99337e-05 | 0.00446825 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687316 | GCGACCACTCGCATG[G/T]CGCGGCCGGACACGC | 7088 |
rs780350569 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81617281 | TTTTTGGAAAGATAA[C/T]AGATGGCAATATTTG | 7088 |
rs780359964 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668057 | TAATCCCAGCTACAT[C/G]AGGAGGCTGAGGCAT | 7088 |
rs780400662 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652411 | GGTTTAAATGCAGAA[C/T]TTCTCAACCACACTT | 7088 |
rs780411453 | in-del | -/AATT | 1.66139e-05 | 0.00288213 | intron-variant | TLE1 | GRCh38.p7 | 9:81613538 | TGGTGTCATTAAACA[-/AATT]AAATGAGTATTATTT | 7088 |
rs780420765 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615544 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAA | 7088 |
rs780423487 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81605320 | GAGAGTGAGCGACAG[A/C]AACCTGAGGACTTAG | 7088 |
rs780437159 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81611721 | ACAGCGCTCAATGGA[A/G]CATGCAGCGTTCCTA | 7088 |
rs780454872 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628728 | TTACAGAGTGACAAC[A/G]TGGTCGCTCAGATTA | 7088 |
rs780459362 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634734 | AGATTTTCAGACTCA[C/T]GCTGTTTTCAGAGGG | 7088 |
rs780524615 | snp | G/T | 1.71578e-05 | 0.00292893 | missense | TLE1 | GRCh38.p7 | 9:81610272 | TGGTAGGTACTCTCA[G/T]GTGAGGGGGAGGATC | 7088 |
rs780554339 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632122 | TCTATAGGAACCCTG[G/T]AATGGCAAAACAATA | 7088 |
rs780606201 | snp | C/G | 6.25958e-05 | 0.0055941 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687469 | GGGACCGAGGGACGG[C/G]AATGCGGGCGGATGA | 7088 |
rs780608134 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662899 | GTTGCCCAGGCTGGA[A/G]TGCAGTGGCATGATC | 7088 |
rs780609589 | in-del | -/GTGTGTGTG | 4.99471e-05 | 0.00499711 | intron-variant | TLE1 | GRCh38.p7 | 9:81633307 | TGTGTGTGTGTGTGT[-/GTGTGTGTG]TGTGTGTGTGCAGCA | 7088 |
rs780615755 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81629917 | CCTAGGCTTCACATT[-/AA]AACAGATTGCTTATT | 7088 |
rs780626062 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640434 | ATTTTACAAAGCAAT[C/T]TGAGAAAGGACTACA | 7088 |
rs780627817 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81594500 | GAACAATGAGATCGC[A/G]CCACTGCACTCCAGC | 7088 |
rs780645753 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81585431 | TCCAGATTATGATCT[C/G]TACCATATTTTTTTA | 7088 |
rs780682032 | snp | A/C | 1.64817e-05 | 0.00287064 | missense | TLE1 | GRCh38.p7 | 9:81616662 | TCATTAGACACATCC[A/C]CAACTAAGTTGTCAT | 7088 |
rs780685688 | snp | A/C | 7.51738e-05 | 0.00613036 | intron-variant | TLE1 | GRCh38.p7 | 9:81600163 | TCTTGGATGGAAAGT[A/C]AAACAAAAAGAGGCT | 7088 |
rs780707189 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633324 | GTGTGTGTGTGTGTG[C/T]GCAGCAGGCGTTTGA | 7088 |
rs780713659 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681556 | TTCCGTCGCGCAAAA[A/G]AAAAAAAGAAAAAAA | 7088 |
rs780737749 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81662333 | TAGATGATGCAGGAG[A/G]CACGGTGTTAGTATT | 7088 |
rs780739953 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599852 | AACTTCAAAGCATTA[A/G]GTTGGGAGACTCTTT | 7088 |
rs780753603 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674675 | TGAGGGGTCAGAACA[A/G]AGAGAGGAGGACTTT | 7088 |
rs780771815 | snp | A/C | 1.68204e-05 | 0.00289999 | intron-variant | TLE1 | GRCh38.p7 | 9:81616147 | GTCCTCAACAAGCAT[A/C]ATCAAAAGTTTTCGT | 7088 |
rs780779876 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586881 | AAAATGTTAACAGGA[A/G]TATGAAATTTAGAAG | 7088 |
rs780782655 | snp | A/G | 7.25466e-05 | 0.00602229 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611817 | CGCGGCGGCTGCGGC[A/G]CTCATCTGGGGCGAC | 7088 |
rs780810750 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668653 | TCGTATGGGACAGAA[A/T]CTATTCAGAGTTACA | 7088 |
rs780835919 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81660365 | AAAAACAAAATCATA[C/T]GTTGGTAAGTATAAA | 7088 |
rs780862643 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603583 | AACTTACCAAAATAA[A/C]CTTTGTCTCCCACAA | 7088 |
rs780887683 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81613465 | GCCCGGCGTTGGCAT[A/G]TCGCTCCGAGGCGTT | 7088 |
rs780934441 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656413 | TACATTCCTCTTCTC[-/G]GAAATTCACATTGAA | 7088 |
rs780934741 | snp | A/G | | | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81686667 | AAACTAACCTTTCTG[A/G]GAAGTTCACTATTGG | 7088 |
rs780944717 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650798 | GTGTAATAAAGCAGC[C/T]TGAATAAAATTTAAG | 7088 |
rs780945289 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81623935 | TCCTCCTGCTCCTTT[A/C]ATCTGGAGGACTAGG | 7088 |
rs780963334 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655858 | ACCCTGTCTCAAAAA[-/A]AAAAAAAAAAAGAAA | 7088 |
rs780988757 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670480 | ACAGGCGTGCGCCAC[C/T]GTGCCCAGCTTATTT | 7088 |
rs780989156 | snp | C/T | 5.02088e-05 | 0.00501018 | intron-variant | TLE1 | GRCh38.p7 | 9:81585474 | CATTTGGGCCATCAA[C/T]GGCCTCCAGTTTCCT | 7088 |
rs780998751 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622831 | TCAAAACAAGGCAGC[A/G]GAGTGTGGGCTGGAA | 7088 |
rs781054518 | in-del | -/CTTTT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632475 | AAATGTTCAGTATCC[-/CTTTT]TTTTTTTTTTTTTTT | 7088 |
rs781062613 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81616688 | GTCATCGCTTTTGTC[A/G]CCATCACTGTCCTGG | 7088 |
rs781088061 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81631240 | ACCCTCCCTCCACCC[A/G]CTCCAATGAACCCAT | 7088 |
rs781100330 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618247 | TAAACAATTCTCTTA[C/T]TGATGCTGTTGTCAG | 7088 |
rs781168978 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81677634 | ACCAAGAGGTTGTAC[A/G]TATACCTAGACTAGT | 7088 |
rs781172780 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81654203 | TTGAAATAAACAGTA[C/G]ATATTAATCCCACTT | 7088 |
rs781196044 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81628510 | CCTCCTTGCCTTCTA[C/T]AATGTTGTCATTTTG | 7088 |
rs781206668 | snp | A/G | 3.29717e-05 | 0.00406015 | synonymous-codon | TLE1 | GRCh38.p7 | 9:81584469 | TATGCTGGCTCCATA[A/G]GGGGTCCGCCAAGCA | 7088 |
rs781241312 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81669515 | TACTGTAAAGTAGAA[A/G]TTTTAACTAATACAG | 7088 |
rs781284706 | in-del | -/AAAAG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81681560 | GTCGCGCAAAAAAAA[-/AAAAG]AAAAAAAATTCTTCA | 7088 |
rs781288291 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81671288 | GAAGGCTGAAGCGGG[C/T]GGATTGCTTGAGCCC | 7088 |
rs781296909 | in-del | -/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675708 | CACTAGTTTTTTTTT[-/G]TTTTTTTTTTTGAGA | 7088 |
rs781315549 | snp | A/G | 1.6886e-05 | 0.00290564 | intron-variant | TLE1 | GRCh38.p7 | 9:81685670 | TGAAGTTCAACTAAA[A/G]CTTACCTGTTTGTGC | 7088 |
rs781349859 | snp | C/T | 3.05796e-05 | 0.0039101 | intron-variant, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687466 | AGGGGGACCGAGGGA[C/T]GGGAATGCGGGCGGA | 7088 |
rs781353026 | snp | A/G | 5.10044e-05 | 0.00504971 | intron-variant | TLE1 | GRCh38.p7 | 9:81616161 | TAATCAAAAGTTTTC[A/G]TGATTTAGCTTGTAA | 7088 |
rs781357086 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81609025 | GCCTTAAAGAAAAAG[-/A]AAAAAAAACAACATT | 7088 |
rs781366074 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81599941 | AAAACTTCTTAAAAT[A/G]GATATGTAAAAGAAG | 7088 |
rs781387947 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81666637 | AAAATTAGCCAGGCG[A/T]GGTGGTGCACGCCTG | 7088 |
rs781390984 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684203 | ATTTGCATAATTCAC[A/T]TAAATGACGATAGAT | 7088 |
rs781455078 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81627297 | CAAAAAGAGGTTTTG[C/G]AGGGAAAAATTGTTC | 7088 |
rs781473005 | snp | C/G | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81589398 | GGGTTACAGTGGATA[C/G]AAAGACATTCAATAG | 7088 |
rs781477842 | snp | C/T | 7.85453e-05 | 0.0062663 | intron-variant | TLE1 | GRCh38.p7 | 9:81634048 | ACAACTTTGCAGCAC[C/T]GTAAGAGTATGAGGA | 7088 |
rs781493967 | snp | A/G | 1.70487e-05 | 0.0029196 | intron-variant | TLE1 | GRCh38.p7 | 9:81591060 | TCTCTGTTCTGTAGA[A/G]TAAACATAATTCATT | 7088 |
rs781512422 | snp | A/C | 1.71193e-05 | 0.00292564 | intron-variant | TLE1 | GRCh38.p7 | 9:81652149 | CACACGTAAAGCCAT[A/C]AAATTAATAAGAAAT | 7088 |
rs781525672 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81592492 | TCACTGCTCTCTTTC[A/G]TTGATGGCTGCCCCG | 7088 |
rs781527977 | snp | A/C | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81588409 | TTAGAAAGAGCCCTG[A/C]ATTAGGAAATCTGGA | 7088 |
rs781554548 | in-del | -/GTGTGTGTGTGT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633291 | TCAGAAGGGGACCGT[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 7088 |
rs781562364 | snp | A/C | 3.29739e-05 | 0.00406028 | missense | TLE1 | GRCh38.p7 | 9:81615982 | GTTTTCTTTACCTAC[A/C]AAGCTCATTTCTTTG | 7088 |
rs781574932 | snp | A/C | | | synonymous-codon | TLE1 | GRCh38.p7 | 9:81611931 | AGGATATGGGCCGGG[A/C]ACTGCCAGGGGTGTC | 7088 |
rs781592898 | in-del | -/GTGT/GTGTGTGTGTGTGTGTGTGTCATCCCGCCT/GTGTGTGTGTGTGTGTGTGTCATCCCGCCTGT | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587907 | TGTTAGTTTTGGACC[lengthTooLong]GTGTGTGTGTGTGTG | 7088 |
rs781612453 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81584950 | AATGCTCAATAAGTG[A/G]TAGGCACTCATCCAC | 7088 |
rs781629528 | in-del | -/ACA | 3.32474e-05 | 0.00407708 | intron-variant | TLE1 | GRCh38.p7 | 9:81613355 | GAAACCAAACAAAGC[-/ACA]ACAAGAGGCGATGCT | 7088 |
rs781633011 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81603664 | CTCCAGCCCAAAACT[A/C]TTTTTCTTGTCATGT | 7088 |
rs781641234 | snp | C/T | 2.29371e-05 | 0.00338645 | missense, upstream-variant-2KB | TLE1 | GRCh38.p7 | 9:81687415 | AACTTGAAGGGCTGG[C/T]CTGCAGCCTGGTGCG | 7088 |
rs781648478 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81674560 | AATCAGAGTCCTTTT[A/G]CAAAATTATTTCTAT | 7088 |
rs781665210 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81634602 | TCACTCACTCCGAGA[C/G]GGGAGCTGTTTATTA | 7088 |
rs781667298 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81683496 | TGGCTACACCCTGGG[C/G]GCCAGACGTCACCAG | 7088 |
rs781681618 | snp | C/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655948 | ATCTTCTAAGATGAT[C/G]TGAATTAACTAAGCA | 7088 |
rs781694397 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81673604 | TAATTACCCTATGGG[A/G]TAGGTGCTACTGTCA | 7088 |
rs781702678 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644720 | CGAATTTGGCCAGGT[A/G]CAGTGACTCATGCCT | 7088 |
rs781712520 | in-del | -/AGACAGTCGAGCTGGGAGACAGGGCTCTTATTGCCAGGG | 1.69407e-05 | 0.00291034 | splice-acceptor-variant | TLE1 | GRCh38.p7 | 9:81591053 | TAATTGTCTCTGTTC[lengthTooLong]TGTAGAATAAACATA | 7088 |
rs781729537 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81622249 | CCAGACTCTGTGCAG[C/T]ATCCACGGCAGGGCT | 7088 |
rs781750335 | snp | A/C | 1.69657e-05 | 0.00291248 | intron-variant | TLE1 | GRCh38.p7 | 9:81620421 | AAACAAATATTATTT[A/C]AAGTCCTTTAATTAC | 7088 |
rs781756463 | snp | A/G | 3.40287e-05 | 0.0041247 | intron-variant | TLE1 | GRCh38.p7 | 9:81585690 | CTCACTCATTATTCC[A/G]CCTGATACACTTAGG | 7088 |
rs781778374 | snp | A/T | 1.74333e-05 | 0.00295235 | missense | TLE1 | GRCh38.p7 | 9:81610289 | TGAGGGGGAGGATCA[A/T]ACCCCACCTGGAAAC | 7088 |
rs796086368 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642408 | ATGAAATTGGGGTCC[A/G]AGGTCCGGGCACAGT | 7088 |
rs796126416 | in-del | -/CC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81667723 | TATTCCTGCTCCCCC[-/CC]AAGCTGAGTGGCTGG | 7088 |
rs796157576 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81668181 | TCGAAAAAAAAAAAA[-/A]GAAGGATATGTAAAG | 7088 |
rs796188532 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81682360 | CCCAGACTCTGAACA[C/T]GTGCACACAGCTGTA | 7088 |
rs796233885 | multinucleotide-polymorphism | AG/TA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81641230 | TAAATAAATAAAAAT[AG/TA]AGAAGAAAACTGGTA | 7088 |
rs796236538 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81651166 | AGGGAACTATAAAGA[C/T]CAGCAGGGCATCATC | 7088 |
rs796241666 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81656187 | AACAGAACTGGGTCA[A/G]CCCCACCCAGTTCAT | 7088 |
rs796242520 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81675779 | GATCTCAGCTCACCA[C/T]AACCTCCAACCCCCT | 7088 |
rs796250559 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679312 | TTCTTCACTTTTTTT[-/T]CTTTTTTTTTCCCCT | 7088 |
rs796260047 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607061 | GACCCAGTGTCTCTA[-/A]AAAAAAAAAAAAAAT | 7088 |
rs796260872 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632090 | CGAAGACTCCATCTC[-/A]AAAAAAAAAAAGACT | 7088 |
rs796262069 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81597288 | CACGACTTAAAAAAA[-/A]GCCAAGTGAAGATAC | 7088 |
rs796290495 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81642544 | TTAAAAAAAAAAAAA[-/A]TTAGCCAGGCATGGT | 7088 |
rs796335328 | snp | A/C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81615542 | CATCTCTACTAAAAA[A/C/T]ACAAAAAAAAAAAAA | 7088 |
rs796365370 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81658534 | ACTATACTGACAAGC[C/T]AGCTTGACTTTTGAG | 7088 |
rs796370623 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81684176 | AAAGATTAAACCGCC[A/T]AGGCCAAGTTTATTT | 7088 |
rs796399998 | multinucleotide-polymorphism | GAG/TAT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81606800 | ACCATATATATATAT[GAG/TAT]GAGAGAGAGGCAGTA | 7088 |
rs796405076 | in-del | CATCCCGCC/GTGTGTG | | | intron-variant | TLE1, LOC105376106 | GRCh38.p7 | 9:81587928 | GTGTGTGTGTGTGTG[CATCCCGCC/GTGTGTG]GTGTGTGTGTGATCC | 7088 |
rs796432236 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586018 | GTGTCGTTAGGTGAC[-/T]TTTTTTTTTTTTTTT | 7088 |
rs796432982 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586034 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTTGC | 7088 |
rs796457291 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81591435 | TATGTTTCGGTCTTC[A/G]TTATGCTGAGCACAT | 7088 |
rs796565830 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632496 | TTTTTTTTTTTTTTT[A/T]ACCATATTAAACACA | 7088 |
rs796578432 | in-del | -/AG | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640748 | TTGCTGTTTACATTC[-/AG]AGTGTTACTGTAATG | 7088 |
rs796583087 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81644085 | GGAGAATAAAAAAGA[C/T]GGACAGGAAATGCCA | 7088 |
rs796583697 | in-del | -/AA | | | intron-variant | TLE1 | GRCh38.p7 | 9:81607074 | CTAAAAAAAAAAAAA[-/AA]TGGAGAGAGAGAGAG | 7088 |
rs796584050 | snp | A/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81625912 | ACCTCAGAAACTACT[A/T]AAAAAAAAAAAAAAA | 7088 |
rs796586720 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81655590 | TTTTTAAAAAAGAAA[A/G]AAAAAGTCATCTGTA | 7088 |
rs796647792 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81639589 | TGTTTTTTTTTTTTG[G/T]TTTTTTTTTTTTTGA | 7088 |
rs796655137 | snp | A/G | | | missense | TLE1 | GRCh38.p7 | 9:81590952 | ATGCGCGGGGTTGGA[A/G]CCGCCAGGTCCCAAA | 7088 |
rs796709532 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | TLE1, LOC105376106 | GRCh38.p7 | 9:81586019 | TGTCGTTAGGTGACT[-/TT]TTTTTTTTTTTTTTT | 7088 |
rs796738531 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81636831 | AAGATGGTGAAACCC[-/C]GTCTCTACTAAAAAT | 7088 |
rs796769603 | snp | A/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650710 | AAAATGTGATACTGA[A/C]GGAGGGGGAAGGCAG | 7088 |
rs796771120 | snp | G/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685231 | AGAATACTCCACAGA[G/T]AGTCATATACCTTGA | 7088 |
rs796790093 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | TLE1, LOC101927502 | GRCh38.p7 | 9:81688494 | CAGCTGCTTCAAGAA[C/T]CTGCGCGGAGACGTC | 7088 |
rs796790898 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633289 | TGTCAGAAGGGGACC[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 7088 |
rs796794091 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650157 | GGACTAAAGCCATTC[A/G]TAAAATTAGAAATTC | 7088 |
rs796796113 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81618951 | CCAACATACTCTCCA[C/T]ACATGGTCCCTAACC | 7088 |
rs796820437 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81679411 | ACCATACTTTTGTTA[A/G]ATCAGGTGAATGGCA | 7088 |
rs796820926 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81630828 | TGCTTTTCATACTCA[C/T]TTTTATACAAAGTTT | 7088 |
rs796827239 | snp | C/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81670428 | CCTCCCGGGCTCAAG[C/T]GATTCTTCTGCCTCA | 7088 |
rs796846638 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81650719 | TACTGAAGGAGGGGG[A/G]AGGCAGTGCCTGGAT | 7088 |
rs796862070 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81645379 | TCCAAAAAAAAAAAA[-/A]TAATAGTAATAATAA | 7088 |
rs796882684 | snp | A/G | | | intron-variant | TLE1 | GRCh38.p7 | 9:81604773 | CACTCATCCACCTGC[A/G]CATGGATCCCTCAAG | 7088 |
rs796883301 | in-del | -/TGT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81633274 | TGTGTGGAGAAGTGT[-/TGT]CAGAAGGGGACCGTG | 7088 |
rs796893265 | in-del | -/TT | | | intron-variant | TLE1 | GRCh38.p7 | 9:81661206 | TATATATATGTATTT[-/TT]ATATATATATATATC | 7088 |
rs796894651 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81680890 | TTAGGGGGAAAAAAA[-/A]TCTCAAAGTGAGAAA | 7088 |
rs796917429 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81685102 | ATATGCTCTGGCCAT[-/A]AAAAAGATGCTTTTT | 7088 |
rs796929593 | in-del | -/T | | | intron-variant | TLE1 | GRCh38.p7 | 9:81643255 | TTTGGTTTTTTTTTT[-/T]GACAGAGTTTCGCTC | 7088 |
rs796940716 | in-del | -/A | | | intron-variant | TLE1 | GRCh38.p7 | 9:81640411 | TAAAAAAAAAAAAAA[-/A]TCCTTGTATTTTACA | 7088 |
rs796959778 | in-del | -/C | | | intron-variant | TLE1 | GRCh38.p7 | 9:81652962 | AAGGCAAAGGAAGGA[-/C]CTCCAGCCTCAATTC | 7088 |
rs796992684 | in-del | -/CC | | | intron-variant | TLE1 | GRCh38.p7 | 9:81632473 | TTAAATGTTCAGTAT[-/CC]CTTTTTTTTTTTTTT | 7088 |