SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs870371 | snp | C/T | 0.188631 | 0.242351 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022724 | AGGAGAGGATGCCCA[C/T]AGCCTTGGGTAGCCA | 114088 |
rs873913 | snp | A/G | 0.318656 | 0.240388 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004874 | ACGTCTAATTCCCAA[A/G]GTTTCTTTCTGTTTC | 114088 |
rs873914 | snp | G/T | 0.499995 | 0.00159744 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005127 | ATAACCCTGAACGCA[G/T]GTTTTGAGTCCATGC | 114088 |
rs873915 | snp | A/C | 0.44768 | 0.153045 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005906 | CTCTCTTATTAGCTA[A/C]GGATTTAACTGACCC | 114088 |
rs875204 | snp | A/G | 0.29278 | 0.246313 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027510 | TGACTGGAGGGATTC[A/G]CAGGACAGATTCCTG | 114088 |
rs875205 | snp | A/T | 0.471292 | 0.116318 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027781 | GAGCAGGCAATAATA[A/T]GAGAGGCATATTTTA | 114088 |
rs875206 | snp | A/C | 0.36021 | 0.224397 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027936 | ACACTTAGATGTTTC[A/C]GTACAGAAGTAAAAT | 114088 |
rs875207 | snp | A/G | 0.471004 | 0.116864 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027950 | CAGTACAGAAGTAAA[A/G]TTGATTTGGTTACAC | 114088 |
rs882413 | snp | C/T | 0.3742 | 0.216966 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028680 | AATATCCAAGAAATC[C/T]GAATGTCACTGCTTA | 114088 |
rs882414 | snp | C/T | 0.473174 | 0.112665 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028413 | GCTTATAAATGTGAT[C/T]AAAATACCAACCTAT | 114088 |
rs882415 | snp | A/T | 0.473174 | 0.112665 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028403 | GTGATTAAAATACCA[A/T]CCTATAAAAACAATG | 114088 |
rs883690 | snp | A/G | 0.380138 | 0.213458 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976642 | CCAGGGTTCTGGCCT[A/G]TCCTAATTATAGAGC | 114088 |
rs883897 | snp | C/T | 0.191461 | 0.24305 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020890 | TCACCATGTGACTGT[C/T]GCAAACTGTTCACCA | 114088 |
rs885251 | snp | C/G | 0.494855 | 0.0504572 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990995 | GGTATTTTAAGCTTT[C/G]TTAAGTGTGGCATTA | 114088 |
rs946621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027580 | TGCCTCTTGGAGCCT[A/G]AATACATAGAGCAAA | 114088 |
rs946623 | snp | A/G | 0.191461 | 0.24305 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020636 | TGGCTTTCACGCATC[A/G]CTGGGATGCCACATC | 114088 |
rs1016302 | snp | C/T | 0 | 0 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975228 | AGTTTTTATCTATTG[C/T]GGATGACAATTCACC | 114088 |
rs1049371 | snp | C/T | 0.310386 | 0.242597 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975952 | CATTCACAGCCTAAT[C/T]TTCTGGAGTAGTCCA | 114088 |
rs1538616 | snp | A/G | 0.111928 | 0.208413 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988754 | GAGAATTGCTTGTTT[A/G]GTTAAGCTGGGATCA | 114088 |
rs1556926 | snp | A/G | 0.467132 | 0.12391 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029303 | AGCCATCAAGCTGCC[A/G]GTGCTTGTTTGCCGC | 114088 |
rs1556927 | snp | G/T | 0.498547 | 0.0269177 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029178 | TTGTCCCAGTTTATC[G/T]CTATCCAATATTTGT | 114088 |
rs1556928 | snp | A/G | 0.372794 | 0.217765 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029082 | CTTCTGCCTGGGCAC[A/G]CTCAGCAGCTTGGGC | 114088 |
rs1556929 | snp | C/G | 0.325563 | 0.238307 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028980 | CGTCCTCCACAGTCA[C/G]TCCCAGGGTAAGTGC | 114088 |
rs1953874 | snp | C/G | 0.271432 | 0.24908 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019223 | CAGTATTCCAACAGT[C/G]AGCAGAGCACACTGG | 114088 |
rs1953880 | snp | C/T | 0.464203 | 0.128908 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013346 | CCAGAAATAAACTCT[C/T]ACATACTTGCTCAAA | 114088 |
rs1953881 | snp | C/T | 0.464203 | 0.128908 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013162 | gatcaaagaactaaa[C/T]acaaaacctaaaact | 114088 |
rs1953882 | snp | A/G | 0.464309 | 0.12873 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012971 | ccaacagtatgaaat[A/G]tttgaaaatcatata | 114088 |
rs1953883 | snp | C/G | 0.283684 | 0.24772 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012853 | tgattagcagcgagg[C/G]tacacaaacagccga | 114088 |
rs1953887 | snp | C/G | 0.282895 | 0.247826 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008398 | TCTTTTTAACTGTTT[C/G]TTTTGAAATACACAA | 114088 |
rs1953888 | snp | C/T | 0.040671 | 0.13668 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008281 | AAACCAGGAAGTTGA[C/T]ACTTAACAGTGTGTG | 114088 |
rs1953889 | snp | A/T | 0.197703 | 0.244469 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007954 | TGTATGCTTTTATCA[A/T]AGAGAGATTATATAA | 114088 |
rs1953890 | snp | A/G | 0.198634 | 0.244666 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007746 | TTTTTGAAATAGTGT[A/G]TAGATTGGAAATAAG | 114088 |
rs1953891 | snp | A/G | 0.225893 | 0.248835 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023169 | TTTTGATAAATTTAA[A/G]TGATAAATATTTATC | 114088 |
rs1953892 | snp | A/G | 0.492823 | 0.0594727 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020286 | GATACAGGCCTCCAC[A/G]GCTCGCTCGCTCTCC | 114088 |
rs1953893 | snp | A/G | 0.313082 | 0.241911 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019970 | TGAGTGTGTACTTAC[A/G]CAGTCTTTATAATCT | 114088 |
rs1959529 | snp | C/G | 0.493748 | 0.0555599 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016754 | CTTTGGCACCAGGGA[C/G]CAGTTTCATGGAAGA | 114088 |
rs1959532 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003576 | GTTTTAATTACACAT[A/G/T]ACATCATGTATTTCA | 114088 |
rs1959533 | snp | A/T | 0.404559 | 0.196498 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985194 | AAGGCTGATTTCAGC[A/T]AAGCTAGACTTGTGT | 114088 |
rs1959534 | snp | C/T | 0.498392 | 0.028309 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984831 | AATGTACTGAAATAT[C/T]GTTACAGTCTTTGTA | 114088 |
rs1959535 | snp | A/G | 0.103082 | 0.202275 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980071 | TCCAATTTCTCATGC[A/G]TGTGGTTTAGGTGCA | 114088 |
rs1959536 | snp | A/C | 0.215747 | 0.247642 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980053 | TGGTTTAGGTGCAAC[A/C]AAAGTGCTTCTTATT | 114088 |
rs2039795 | snp | C/T | 0.289165 | 0.246913 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011035 | TGGCCTTCCAGGTCC[C/T]CCACCATCCACGCAA | 114088 |
rs2105230 | snp | C/T | 0.233818 | 0.249476 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005990 | AAGAAAGTAGGTTTG[C/T]AGTTGGCTTTTACGT | 114088 |
rs2275460 | snp | A/G | 0.252421 | 0.249988 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987416 | GAAAAGCTAACTTTA[A/G]TATTGTAAGTTCAGA | 114088 |
rs2275461 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987380 | ACTCTTGGAGGTATT[A/G]AATTAAAACTTGCCA | 114088 |
rs2275462 | snp | A/C | 0.476929 | 0.104895 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979498 | GGTCCTCCTCGACTT[A/C]AATAGAAAAAACTTG | 114088 |
rs2275463 | snp | C/G | 0.134494 | 0.221717 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979251 | TGAAGGAGAGGAGGA[C/G]AGAAAGGGATCAGCA | 114088 |
rs2297889 | snp | A/T | 0.40118 | 0.19911 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009076 | TGCAAGTGAAAGGTA[A/T]GTCCTTGCATCCCCC | 114088 |
rs2356732 | snp | C/T | 0.313082 | 0.241911 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027106 | GCACAGTGCATGATG[C/T]GTGCTTAATAAATGC | 114088 |
rs2356733 | snp | A/G | 0.450859 | 0.148847 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027243 | CTGCCTCCCAGGTTC[A/G]AGCGATTCTCCTGCC | 114088 |
rs2884018 | snp | A/C | 0.450734 | 0.149016 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027261 | CGATTCTCCTGCCTC[A/C]GCCTCCCGAATAGCT | 114088 |
rs2999394 | snp | A/G | 0.490836 | 0.0670685 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093311 | TAACTACTGAAAGAG[A/G]AAAGGGCTTGAATTC | 114088 |
rs3007082 | snp | C/T | 0.233527 | 0.249457 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089863 | TTGACTGGTGAGACA[C/T]TGACTCTGTTTGACA | 114088 |
rs3007083 | snp | G/T | 0.271702 | 0.249056 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091822 | TTTTAACATTCTTTT[G/T]TGGCAGGTAGATATC | 114088 |
rs3007084 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093755 | GAGCGTGCCTAGCGG[C/T]CCTGGGCACTGGCGC | 114088 |
rs3029459 | in-del | -/CCAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005555 | GAAATCTATTCTCAA[-/CCAA]ACAGTAAAGCCCTTG | 114088 |
rs3029461 | in-del | -/A | 0.399253 | 0.200558 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007801 | AACACATATTAAACC[-/A]AAAAAAAAAAAAAAA | 114088 |
rs3742326 | snp | C/T | 0.0592355 | 0.161582 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976987 | TAACTTAATTTTTTA[C/T]GTAGGTGAGTTATAT | 114088 |
rs3813398 | snp | C/G | 0.485324 | 0.0843964 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997105 | ATCCCGGTGAGGTGG[C/G]GGGGTGATTTCTTTG | 114088 |
rs3829761 | snp | A/G | 0.386694 | 0.20932 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095209 | GCCCATTGGGCGGGG[A/G]GCAAGAGATCGAAGC | 114088 |
rs3900632 | snp | G/T | 0.140242 | 0.224618 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023632 | AAATCAAATAAAAAG[G/T]TTATATCCAGCATTT | 114088 |
rs4077264 | snp | A/G | 0.240765 | 0.249829 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063859 | tttttagtgtcaagc[A/G]gattgaaacaagatt | 114088 |
rs4077265 | snp | A/T | 0.445592 | 0.155704 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064135 | ctgatatttgatgtg[A/T]atgttagctgtaggc | 114088 |
rs4077266 | snp | G/T | 0.322245 | 0.239334 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064679 | TCTATAGGATTTTTT[G/T]TGTGTGTGATATCCT | 114088 |
rs4131106 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072051 | TTCCTTCCTTCCCGG[G/T]GTTCTCTGGGCTGCC | 114088 |
rs4243567 | snp | C/T | 0.377977 | 0.21476 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033241 | GGGACTACAGGTGTG[C/T]GCCACCACACCTGGC | 114088 |
rs4243568 | snp | C/T | 0.485799 | 0.0830599 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056436 | CAAAATAAGCAAATT[C/T]ATCATGAAATAATCC | 114088 |
rs4243569 | snp | A/G | 0.482831 | 0.0910472 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069428 | TATCTAGAGGCCAGG[A/G]ATACAGTTCAACATC | 114088 |
rs4268677 | snp | A/T | 0.498253 | 0.0295011 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077616 | CCAGGCTTGTCTCAA[A/T]CTCCTGTCCTCAGGT | 114088 |
rs4337215 | snp | C/G | 0.145642 | 0.227177 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077185 | TCCTTTGCAGTTGGC[C/G]AACAAGCACTGATTT | 114088 |
rs4343172 | snp | C/T | 0.39979 | 0.200158 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083489 | TTCTCAAACTCCTTC[C/T]GCCTCAGCCTCCCAA | 114088 |
rs4354845 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074334 | TAAATAATGGTATGT[A/G]AAAATCTAACAATCA | 114088 |
rs4357855 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036266 | TATGTATTTACACCA[G/T]AGAAATTGGCAAACA | 114088 |
rs4375571 | snp | C/T | 0.433963 | 0.169285 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048220 | GGAAAATTCAGTGCA[C/T]GGGCAATCTCTGCCT | 114088 |
rs4389065 | snp | A/G | 0.493386 | 0.0571263 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074890 | ATGAAAGATGCCGCA[A/G]CTACATGGTTCATCT | 114088 |
rs4400967 | snp | A/G | 0.326035 | 0.238157 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081822 | atggcagagacgcat[A/G]gagtaaggtactagg | 114088 |
rs4418980 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035623 | AGAACGCTATACCAC[C/G]CGGAAGAACATGGTG | 114088 |
rs4426259 | snp | C/G | 0.397633 | 0.201754 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083575 | AATACTTTGCAGCAG[C/G]ATTCTTCACACGTCT | 114088 |
rs4444245 | snp | A/C | 0.49089 | 0.0668743 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084351 | AAGTAAAAAGTAGAG[A/C]AAATTCTATTTAATA | 114088 |
rs4447338 | snp | C/T | 0.398174 | 0.201356 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083358 | CTGGGCTCAAGTGAC[C/T]CTCCTGCCTCAGGAG | 114088 |
rs4450305 | snp | C/T | 0.397633 | 0.201754 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083529 | ATTACAGGTGTGAGG[C/T]ACCATGCCCAGCAGA | 114088 |
rs4479142 | snp | C/T | 0.432742 | 0.184336 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064179 | TTAGAACATAGACTG[C/T]GTATATTGACTATGA | 114088 |
rs4480710 | snp | C/G | 0.398534 | 0.201091 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059365 | AAATGCAGGCCATCC[C/G]TTAAAATATACAGAT | 114088 |
rs4496046 | snp | C/T | 0.397994 | 0.201489 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083406 | ACTACAGGCATGCGC[C/T]ACCATGCCCAGCTAA | 114088 |
rs4505215 | snp | A/G | 0.286825 | 0.247273 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074728 | CGCCCAGGATAAGGG[A/G]GCAGAGCTCAAAGCT | 114088 |
rs4516123 | snp | A/G | 0.325091 | 0.238456 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066273 | cttcaaccaattccc[A/G]tcagacttttcatcc | 114088 |
rs4516135 | snp | A/G | 0.482083 | 0.0929373 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035352 | GTGGAAACTTGAGGG[A/G]TGAATAAGAAGTCTA | 114088 |
rs4526941 | snp | A/G | 0.485799 | 0.0830599 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056117 | TGTACAAAAGCAAAC[A/G]TCTACAATGGTACAA | 114088 |
rs4530045 | snp | A/G | 0.386504 | 0.209444 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057500 | CCTATCTTTTATATT[A/G]TATCTGCTAAAATAA | 114088 |
rs4539521 | snp | A/G | 0.497329 | 0.0364438 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041240 | ATGAAAATAAATCTC[A/G]CCATGGGAATTAGTT | 114088 |
rs4551942 | snp | A/T | 0.499999 | 0.000599041 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026944 | AACAATTCTGAATTC[A/T]GAAATGCTGCCAGTT | 114088 |
rs4606614 | snp | C/T | 0.17654 | 0.238964 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063252 | ATATACTGGAGTAGG[C/T]GGAATAAAAAATTCG | 114088 |
rs4609754 | snp | C/T | 0.177503 | 0.239258 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052207 | AATTATCTCAATATA[C/T]ATTTTTCCAAAATCA | 114088 |
rs4609755 | snp | C/G | 0.446249 | 0.154875 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095476 | GCAGCGAGTGGGCTG[C/G]CGGAGGGGGCTGGGG | 114088 |
rs4616215 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053426 | AGTTCATTCAGTACT[C/T]AGTTTGTATCAGTTT | 114088 |
rs4617764 | snp | C/T | 0.485866 | 0.0828688 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056237 | CCAGAAATTGGTCTA[C/T]AATCAGCAATTCTTT | 114088 |
rs4624086 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070169 | aaatgctgtctagca[C/T]tcctaagcacaagaa | 114088 |
rs4898678 | snp | A/C | 0.0919752 | 0.193722 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999308 | TGAAAATGACACAGG[A/C]ACTGAAAAGGCAAAG | 114088 |
rs4898679 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036123 | CTTTTTGCCATGCCC[C/T]GAGGCAAAAAGTGGC | 114088 |
rs4898680 | snp | A/C | 0.499994 | 0.00179711 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060082 | ATAAATCACCTCCTG[A/C]CTGGAATACTTCAGA | 114088 |
rs4898681 | snp | A/G | 0.172997 | 0.237846 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085455 | CAGTTTTATTTGGCA[A/G]TGTTTAAATCCATTC | 114088 |
rs4901069 | snp | A/G | 0.499464 | 0.016365 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980721 | GTTCCACAAAATGCC[A/G]ATCACTGAAGATAAC | 114088 |
rs4901070 | snp | C/T | 0.141258 | 0.225111 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985847 | GCCACAGACAGAGAC[C/T]AGCTCATCCCCCTCA | 114088 |
rs4901071 | snp | A/G | 0.290201 | 0.246747 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003868 | TTGTATATAAAAGGT[A/G]AATGTGCCAAAATTA | 114088 |
rs4901072 | snp | A/G | 0.376394 | 0.215696 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035933 | CTGACAGAGCCTTGT[A/G]CAGAGTAGTAGTGAC | 114088 |
rs4901073 | snp | A/G | 0.495174 | 0.0488838 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048745 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGCAGGCG | 114088 |
rs4901074 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051570 | CATTTATATAGCTTG[C/T]TATTGTGGGTGTAAT | 114088 |
rs4901075 | snp | C/T | 0.385741 | 0.209939 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056701 | CTTAGGCCATTATCC[C/T]TACTCCCAGTTTCAC | 114088 |
rs4901076 | snp | A/G | 0.397994 | 0.201489 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085408 | GTTAGTATAAAACAC[A/G]CAGTTCTGCTTCTAT | 114088 |
rs4901077 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093004 | GCTGAATGAACACCA[A/C]ATGCAAAGGCCCTGG | 114088 |
rs4901078 | snp | A/G | 0.0414363 | 0.137845 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51096063 | AGTGCCCGTAGTTTA[A/G]TAAAGCTCTGTAAAT | 114088 |
rs5003887 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000144 | CAATTAAGAGGAATG[C/T]CAATCAAAGACATTA | 114088 |
rs5012096 | snp | A/T | 0.246857 | 0.24998 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083431 | AGCTAATTAAAAAAA[A/T]TTTTTTTTTTAGAGA | 114088 |
rs5808588 | in-del | -/T | 0.191473 | 0.243053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021993 | CAATTCAAAAACACA[-/T]TTTTTTGCCTGTGTA | 114088 |
rs5808589 | in-del | -/T | 0.463666 | 0.129795 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027837 | ATATCTTTTTTTTTT[-/T]CCTGAATGAGTAAAA | 114088 |
rs6572717 | snp | C/T | 0.179744 | 0.239925 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984260 | CATTTTATTTTCTTT[C/T]CTATTTAGTAAGGCC | 114088 |
rs6572718 | snp | C/T | 0.403334 | 0.197456 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025810 | GGAAGGGGTAGGTAC[C/T]GGTGTGATCCTCTGG | 114088 |
rs6572719 | snp | C/T | 0.332106 | 0.236133 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025946 | ATTTGTGTCCTCTCC[C/T]CACTAGCCTCCGACA | 114088 |
rs6572720 | snp | C/T | 0.246485 | 0.249975 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029484 | GGAAAAAAGTGATCA[C/T]TGATGCAATGGGACT | 114088 |
rs6572722 | snp | C/T | 0.385741 | 0.209939 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057005 | AAAAGAATGAATAAA[C/T]GAACCCATCTCCTAT | 114088 |
rs7140807 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005417 | GTTAGGTCATTGTTT[C/T]GTCCTGGTTCAGAAT | 114088 |
rs7141683 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023160 | ATTAAAAGGGATAAA[C/T]ATTTATCACTTAAAT | 114088 |
rs7143008 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040771 | ATGATGAACCACAGA[C/T]TCCTTCTCTGTTAGT | 114088 |
rs7143279 | snp | A/G | 0.180064 | 0.240019 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993618 | ggagatctgcccAAC[A/G]TGACTGCAAGTAGTA | 114088 |
rs7144184 | snp | A/C | 0.407674 | 0.194008 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009790 | TAGCCAGTTTAGTAG[A/C]GTGTGACTTGGAAGA | 114088 |
rs7145511 | snp | A/G | 0.430732 | 0.172731 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016263 | gactggcactggtcc[A/G]tggcctgttagaaac | 114088 |
rs7147409 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026012 | CCCATCCATACGAGG[A/T]GGCAGTTCTGCTGGG | 114088 |
rs7147763 | snp | C/G | 0.316726 | 0.240931 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026111 | AATCCTGACGGACGA[C/G]ACCTAAGTGGAAGTC | 114088 |
rs7147946 | snp | C/T | 0.344592 | 0.231414 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026243 | GGATGTGATGTCTTC[C/T]GGCTCACATGAGGAG | 114088 |
rs7148279 | snp | A/T | 0.131381 | 0.220067 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065031 | TTACAGTCCTTCAAA[A/T]CCTAGGGAATCAAGA | 114088 |
rs7149252 | snp | C/T | 0.368938 | 0.219895 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072034 | AAGGAAACTTTCCTT[C/T]CTTCCTTCCTTCCCG | 114088 |
rs7153154 | snp | A/G | 0.433818 | 0.169443 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018097 | AAGTTGTTCCAGTGT[A/G]CCTAATTTTTCCAAA | 114088 |
rs7155534 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075034 | AGACTCTTGTCAGGA[A/G]CTGAGTCAGAGAAAC | 114088 |
rs7155615 | snp | C/T | 0.353154 | 0.227726 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073048 | TTAGCAGACACCACA[C/T]CAAAGATGATATTCA | 114088 |
rs7156654 | snp | C/T | 0.251296 | 0.249997 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069553 | GAGAAACTGCAAATC[C/T]GAGGCCCTCGGGACA | 114088 |
rs7157686 | snp | C/T | 0.288386 | 0.247035 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011675 | TTTCATTTTTGGTTA[C/T]AAATTTATTTTCCAT | 114088 |
rs7158622 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057524 | AAAATAAAAGATACT[A/C]AATTGAAAATAATTT | 114088 |
rs7158976 | snp | A/G | 0.386313 | 0.209568 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057734 | TGGCCTTTTAATCTG[A/G]ATGTATTCATCTTTC | 114088 |
rs7159294 | snp | C/G | 0.385932 | 0.209815 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057771 | AATGTAGCCTATTGA[C/G]TAGAAAAGTAGGTCA | 114088 |
rs7159320 | snp | C/T | 0.386123 | 0.209692 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057806 | TATAAAATCCCTATG[C/T]TTTGATTTTTGAGAT | 114088 |
rs7160975 | snp | C/T | 0.331179 | 0.236453 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057952 | TTTTGGGCTCTTATT[C/T]CAAGCCAGTTTACTC | 114088 |
rs7161111 | snp | C/T | 0.401037 | 0.199218 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037132 | CCCATCACCTCACTA[C/T]ATTCCTCAAAATGCT | 114088 |
rs7161304 | snp | G/T | 0.168135 | 0.236216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082271 | Gatactcaaggtaat[G/T]gaaaacatgtccaca | 114088 |
rs7161450 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987281 | ACTTCTATCAAAATG[C/T]TACTCGCATGTTGAA | 114088 |
rs7493564 | snp | A/G | 0.434109 | 0.169127 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047338 | CATCACTCTGACAGC[A/G]TCTGGGCCACGGCAT | 114088 |
rs7493780 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072344 | ATCCAACGAGAATTC[C/G]TAAACCTCTGAAATG | 114088 |
rs7493839 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999211 | TCAAGACAAAATAAG[A/G]TAATTATTTAAAGAA | 114088 |
rs8003601 | snp | A/G | 0.199873 | 0.244923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005472 | TACCATGACTCATGA[A/G]TCTTGGGATTCTTTG | 114088 |
rs8004486 | snp | C/T | 0.209388 | 0.246679 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015948 | TATGCCTTCCCATTA[C/T]AGTTTAAAACAATTT | 114088 |
rs8005389 | snp | C/T | 0.323908 | 0.238825 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040576 | CTCTGCTCATACTTT[C/T]ACCCACTCTGAGAAG | 114088 |
rs8006268 | snp | G/T | 0.117188 | 0.211804 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006164 | ATACTTTAAGTAAAT[G/T]TGAAAATATTTTAAC | 114088 |
rs8006348 | snp | A/G | 0.400147 | 0.19989 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058755 | CCCTTCAATTCAGCT[A/G]CATATGGTGTGACTC | 114088 |
rs8006878 | snp | C/T | 0.39979 | 0.200158 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058968 | AGGAAAGAAGGGTTG[C/T]GGAATCTTGGGCTGA | 114088 |
rs8007373 | snp | A/G | 0.259674 | 0.249813 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988384 | TTAGAGTAGGTGATG[A/G]CACCCCTTTATAGGG | 114088 |
rs8007631 | snp | A/C | 0.294832 | 0.245947 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980111 | TTATGTTATCCATTA[A/C]ACAGAAAAACTCATT | 114088 |
rs8008268 | snp | C/T | 0.400147 | 0.19989 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059076 | AGTCTGCCAGGCCTA[C/T]GACCAACCCCAATAT | 114088 |
rs8008638 | snp | A/G | 0.240765 | 0.249829 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062304 | atctttgggcatgcc[A/G]tgtagactgctttgg | 114088 |
rs8008731 | snp | C/T | 0.441977 | 0.16014 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067780 | AAGCAACCTCCTTAC[C/T]ACTTCCTTCCAAACA | 114088 |
rs8009082 | snp | A/C | 0.226779 | 0.248919 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032626 | CTGGCTTCCTCACTT[A/C]CAGGTGGATCTACCA | 114088 |
rs8009152 | snp | A/G | 0.117188 | 0.211804 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006264 | TGGACGGATTACTTT[A/G]ATACCACTCCAAATG | 114088 |
rs8009573 | snp | A/C | 0.47802 | 0.102502 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085911 | AGCAGGATGAACCCC[A/C]TCTCTGTCAGGTAAG | 114088 |
rs8009664 | snp | C/T | 0.195526 | 0.243993 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038164 | AATGACATGAGTCCT[C/T]AAAAGCAGAGGAACT | 114088 |
rs8009735 | snp | A/C | 0.397633 | 0.201754 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086012 | GTCACCTCTTTCCTC[A/C]TGCACCACAATTTCT | 114088 |
rs8010154 | snp | C/T | 0.486 | 0.0824865 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062619 | GGATATCAAGGATAG[C/T]CAGGAAAACCTGAAG | 114088 |
rs8010552 | snp | C/T | 0.117188 | 0.211804 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006272 | TTACTTTAATACCAC[C/T]CCAAATGCTACTTCT | 114088 |
rs8010881 | snp | C/T | 0.397633 | 0.201754 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085868 | GGTAAAATCTTACTG[C/T]CTATTTGTTACTTAG | 114088 |
rs8011399 | snp | A/G | 0.341685 | 0.232581 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042232 | AAGACCCAGCCTGTC[A/G]TTGTCCCTACCCAGC | 114088 |
rs8011567 | snp | C/T | 0.29175 | 0.246489 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026053 | GTCCAGGTAGGTACT[C/T]GCTCTTCCAGCCTCC | 114088 |
rs8011740 | snp | A/G | 0.152667 | 0.230274 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994284 | tggtggcacatgcct[A/G]tagtcctaactactc | 114088 |
rs8012256 | snp | A/G | 0.241053 | 0.24984 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059843 | AACAAAAAAACTAAA[A/G]CAAAACAAAACTCTG | 114088 |
rs8012460 | snp | C/T | 0.229136 | 0.249128 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050676 | atcctatgtgccttc[C/T]gaagccaggtcataa | 114088 |
rs8012725 | snp | A/G | 0.244776 | 0.249945 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980670 | AAAAGTAAGTGTGGC[A/G]TTTGGGTGATAGCAC | 114088 |
rs8012734 | snp | A/G | 0.46865 | 0.121211 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060071 | GGGAGTCACAGATAA[A/G]TCACCTCCTGACTGG | 114088 |
rs8013051 | snp | G/T | 0.204496 | 0.245824 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029386 | TCACAGTGCATGCCA[G/T]TCAGGCACCGCAACA | 114088 |
rs8013997 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038399 | gtttcatggcagcaa[C/T]agaaacctaacacaC | 114088 |
rs8014229 | snp | C/T | 0.26078 | 0.249767 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995211 | AATTTAATTAATTTT[C/T]ATTGCTTTCCTAATT | 114088 |
rs8016284 | snp | A/G | 0.486464 | 0.0811471 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065848 | AAGGCCCACTTGAAG[A/G]GGGTGCTTTGACATT | 114088 |
rs8016661 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066087 | ggaaggaaggaagga[A/G]ggagggagggaggga | 114088 |
rs8016963 | snp | A/G | 0.241914 | 0.249869 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066025 | ATTATTTTCATTGGC[A/G]TGCAAGCAGGCCTGA | 114088 |
rs8017382 | snp | G/T | 0.467744 | 0.122832 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995268 | TAATCCCTTTTCCCT[G/T]TTTTTCAGTGTTTAT | 114088 |
rs8018083 | snp | A/G | 0.228253 | 0.249052 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045041 | CAACTTCTGTTGATT[A/G]TCATGTGAAAATATG | 114088 |
rs8018255 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015023 | ACAGTTTCAGAGAAG[G/T]CTTTTAAAATTTTAT | 114088 |
rs8018259 | snp | G/T | 0.477175 | 0.104362 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045115 | TGTTCAAGACTCATT[G/T]GTGGGATTGCTTCAG | 114088 |
rs8019242 | snp | A/C | 0.0267878 | 0.112589 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975010 | gtctaaaaaaaaaaa[A/C]aaaaaaCAGAAGTAA | 114088 |
rs8019404 | snp | A/G | 0.323908 | 0.238825 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040075 | ggcgtgagccattgc[A/G]cccagccAAACTTTT | 114088 |
rs8019409 | snp | A/G | 0.2768 | 0.248559 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975134 | CATGCCCAAGGAAAC[A/G]GGGGAAAGAACACAT | 114088 |
rs8019419 | snp | C/T | 0.499598 | 0.0141716 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015194 | AAGGACTGTTGTGTC[C/T]CTTTGAATTCTCAGA | 114088 |
rs8020721 | snp | C/T | 0.473634 | 0.111748 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978261 | ATAGGGCAAAAGTCA[C/T]CTGTAATTCTCAAGC | 114088 |
rs8022399 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015338 | AGGCAGTTCATGTGA[C/T]ACAACCAGAAGCAAG | 114088 |
rs9707722 | snp | A/G | 0.478271 | 0.101943 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084156 | AAGAGCTTACTATCA[A/G]TTCAAACTTTTCCAC | 114088 |
rs9888603 | snp | C/T | 0.384593 | 0.210677 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993219 | CCTCTCTAGGTGACC[C/T]GCTCACCTGGGATGG | 114088 |
rs9944003 | snp | C/T | 0.412249 | 0.190198 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988338 | ATCATAAATTGTACT[C/T]ACCTTTTCTATTCTC | 114088 |
rs9944007 | snp | C/T | 0.412416 | 0.190055 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988448 | ATTAGTAACTTGGCA[C/T]TAAGATGGTTATGGC | 114088 |
rs9944076 | snp | A/G | 0.330714 | 0.236612 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988098 | TGAGCTACCACACCC[A/G]GACTAAAAGATTTTT | 114088 |
rs9944148 | snp | A/G | 0.330482 | 0.236691 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990295 | GTGTTGAGATTACAG[A/G]CATGAGCCATGGCAC | 114088 |
rs9972233 | snp | C/T | 0.148661 | 0.22854 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050983 | CAAGCCAAGCCAAGA[C/T]GCTGCTGATTCCTAA | 114088 |
rs10129635 | snp | A/G | 0.125528 | 0.21681 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031819 | CTTCAGCAGGCCAAG[A/G]TTACCTTGAAGGATA | 114088 |
rs10129790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031961 | GTGGAGGGCAGAAAG[A/G]AGGAGGGCTCTGTGC | 114088 |
rs10130678 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984812 | TTCTTGAGACAATGT[A/G]CATTACAAAGACTGT | 114088 |
rs10130725 | snp | C/G | 0.24932 | 0.249999 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992076 | TCTTCTTTAAATAGA[C/G]TGTTTAGTTTATGTA | 114088 |
rs10133868 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013613 | TATTGTCACTGGTGA[A/G]AGGAACCAACTCTGA | 114088 |
rs10134544 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980593 | GAATGTGTTTCTCTG[C/T]ATAGTGTGATGGTTA | 114088 |
rs10137286 | snp | C/G | 0.456568 | 0.140818 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014655 | GTATAAATACTTTCT[C/G]TCTAGTTGTCTTTAT | 114088 |
rs10137411 | snp | A/C | 0.288906 | 0.246954 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011290 | ATGACATTCCTTGAA[A/C]AGTTTTTTTCTTCAG | 114088 |
rs10137784 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004317 | TCCTTGAAGAGGTCT[A/G]GCGGAGCTGTGGTTC | 114088 |
rs10137862 | snp | C/T | 0.477684 | 0.103247 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981646 | AACCACCAGCATGGA[C/T]TCAGCTGAGGCTCAT | 114088 |
rs10140156 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082733 | AACTATTGAATTACA[C/T]ACTTTAAAAAGGTAA | 114088 |
rs10140413 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987899 | ctttgcttcctggat[A/C]aagtgattcttcaac | 114088 |
rs10141612 | snp | C/T | 0.117188 | 0.211804 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033619 | CCTTGTCATCCTTGG[C/T]CATACGGCTTGCTTT | 114088 |
rs10142831 | snp | C/T | 0.299916 | 0.244966 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992067 | TACATCTTTTCTTCT[C/T]TAAATAGAGTGTTTA | 114088 |
rs10143878 | snp | A/G | 0.279461 | 0.248258 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016556 | attatgttattatta[A/G]catattaattatatt | 114088 |
rs10147256 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048101 | TACTCACACAAGACT[A/G]TTCTCAATGTTAGAA | 114088 |
rs10148051 | snp | C/T | 0.02016 | 0.0983543 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095747 | TGGCGACACTCTTGG[C/T]TTCTTTCATCCTGCG | 114088 |
rs10149656 | snp | A/T | 0.288906 | 0.246954 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011319 | AGAGGCATTTGTCAT[A/T]TGTGTCCTCTGCTCA | 114088 |
rs10149698 | snp | A/C | 0.133435 | 0.221162 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054084 | TCTTTCTTTAGAAAT[A/C]ATTTTGACATCATTA | 114088 |
rs10149786 | snp | C/T | 0.249038 | 0.249998 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022243 | CCCTGCCTTCATGAA[C/T]GGACGAATGCTATTA | 114088 |
rs10150121 | snp | C/T | 0.499631 | 0.0135733 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981695 | AATGTAGACCACCTG[C/T]TTGATTTCCTGAATG | 114088 |
rs10151348 | snp | C/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036614 | aattgttacactata[C/T]tatttatggaataat | 114088 |
rs10151412 | snp | C/T | 0.280256 | 0.248162 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999923 | TGGTGGTACCACAGC[C/T]GTGTCTTACCAGGAG | 114088 |
rs10152028 | snp | C/T | 0.341235 | 0.232758 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031381 | gctgccaaaagaatt[C/T]gatgttgttccattg | 114088 |
rs10400714 | snp | A/G | 0.122064 | 0.214785 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026686 | TAAATACAAAGTTGG[A/G]CACTGACTCTCTAAA | 114088 |
rs10400783 | snp | A/T | 0.125874 | 0.217008 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026666 | TTTCTCTTATATTTG[A/T]CTTTTAAATACAAAG | 114088 |
rs10444714 | snp | A/G | 0.220544 | 0.248259 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073642 | GAGTGTGGTGTGGGC[A/G]CTCTGGACTGGAAGG | 114088 |
rs10483601 | snp | C/T | 0.143284 | 0.226079 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028349 | AGCACTTTCTAGTGA[C/T]AGTTTTCCAGGATTT | 114088 |
rs10483602 | snp | A/T | 0.498253 | 0.0295011 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018976 | TTTGTTGTTTATGTA[A/T]CATTCACAATTTGAC | 114088 |
rs10483603 | snp | C/T | 0.216048 | 0.247684 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018692 | ACCATGTTGCACAGT[C/T]TTCATATTAATATTT | 114088 |
rs10483604 | snp | A/G | 0.216048 | 0.247684 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018477 | AGAACACAAATTTAC[A/G]TTACGGATATTATTG | 114088 |
rs10483605 | snp | A/G | 0.00631482 | 0.0558349 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010361 | TTAACTAGTTTCTGC[A/G]TCAGATTCTAAATGT | 114088 |
rs10483606 | snp | A/C | 0.448963 | 0.151372 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003420 | ATGAAATGTAGACTT[A/C]CCTGAAACATGAACA | 114088 |
rs10483607 | snp | C/T | 0.195214 | 0.243923 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996604 | TGGCCTCATTTCCCA[C/T]GTGTGTACAAGGTGG | 114088 |
rs10483608 | snp | C/G | 0.392325 | 0.205532 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992010 | GTCCTCTACACAAAC[C/G]TTGGTCCCCACTGAG | 114088 |
rs10569486 | in-del | -/TG | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002106 | TGGGAACCATGGTTT[-/TG]TGTGTGTGTGTGTGT | 114088 |
rs10633847 | in-del | -/AT | 0.495559 | 0.0469148 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025759 | GGCTATTGGTCTGGG[-/AT]TAGGGCAGAAAGAAT | 114088 |
rs10641747 | in-del | -/TGTTGTTGT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054313 | TGTTGTTGTTGTTGT[-/TGTTGTTGT]CCAGGCTGAAGTATA | 114088 |
rs10713868 | in-del | -/G | 0.433673 | 0.1696 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018001 | TTCATCATTCATGAT[-/G]GGCTTGTAATCAATC | 114088 |
rs10873039 | snp | C/G | 0.258843 | 0.249844 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983188 | TGGGGGAAAAGTAAG[C/G]TTTGAGGCATAACAT | 114088 |
rs10873041 | snp | A/G | 0.237303 | 0.249677 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006380 | ATCTTTAAAAAATAA[A/G]AAGATGAACGCCACA | 114088 |
rs10873042 | snp | C/T | 0.476746 | 0.10529 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044124 | TGCACAAGTACTAGA[C/T]TGTAACATGTGATTT | 114088 |
rs11157785 | snp | C/G | 0.489142 | 0.0728777 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984548 | GTTAGAGCATAGTGA[C/G]TATGGAATACCTGGA | 114088 |
rs11157786 | snp | C/T | 0.330714 | 0.236612 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990728 | ATAACTTAAGCAGCC[C/T]TTGAACCCAGGTCCA | 114088 |
rs11157787 | snp | C/T | 0.330016 | 0.236849 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992527 | ACAGTGAGCCACGAT[C/T]GTGACACTGCACTCC | 114088 |
rs11157788 | snp | A/G | 0.416382 | 0.186593 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993123 | GAGCCTCAGAGATGT[A/G]GCTCTGATATTCCTT | 114088 |
rs11157789 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006367 | ACTGACAAAGAATAT[A/C]TTTAAAAAATAAGAA | 114088 |
rs11157790 | snp | A/T | 0.453209 | 0.145623 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015842 | CTCTCTCATCATAGG[A/T]TTTGATGGGATATCA | 114088 |
rs11157791 | snp | C/T | 0.498323 | 0.0289051 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018697 | TTAATATGAAGACTG[C/T]GCAACATGGTAAGCT | 114088 |
rs11157792 | snp | A/G | 0.431473 | 0.171952 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038598 | AGAATCTGGCCCACT[A/G]CAACAATGTGAACAC | 114088 |
rs11157793 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066083 | GGAAGGAAGGAAGGA[A/G]GGAAGGAGGGAGGGA | 114088 |
rs11157794 | snp | C/T | 0.181022 | 0.240296 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067233 | AGCCCGTTTCTGAGG[C/T]CCCCTCCTAATAGTC | 114088 |
rs11157795 | snp | A/G | 0.330947 | 0.236533 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076461 | TGAGGGGAAGCAGCC[A/G]TAAGCATTTCAGCCG | 114088 |
rs11157796 | snp | C/T | 0.255782 | 0.249933 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077905 | CCATTATCTGTGTAA[C/T]GATTATCCATTCTTC | 114088 |
rs11268378 | in-del | -/AGAAGAGGGGA | 0.421209 | 0.182174 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048572 | AGAAGCTGGGGATCC[-/AGAAGAGGGGA]TAGGCACATAAACAA | 114088 |
rs11268748 | in-del | -/CACACAGGTGTTTT | 0.309154 | 0.242901 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025417 | ATACACCAACAAGGC[-/CACACAGGTGTTTT]CCAGCGAGACTCAAA | 114088 |
rs11341604 | in-del | -/T | 0.332106 | 0.236133 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054448 | CAGCTGTTTTTTGTA[-/T]TTTTTTTGTTAGAGA | 114088 |
rs11404701 | in-del | -/T | 0.490063 | 0.0697833 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085430 | GCTTCTATGCAAGGC[-/T]TATGAAAAACAGTTT | 114088 |
rs11429685 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015506 | CTTTCTTTACTTttc[C/T]ttttttttttttttt | 114088 |
rs11455211 | in-del | -/A | 0.490231 | 0.0692021 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028252 | GTTCTGGTATTTGAT[-/A]AAAAAATTGCATTAT | 114088 |
rs11550543 | snp | C/T | 0.13446 | 0.221699 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976815 | GTAGCATACAGCTTA[C/T]CTGCTAGAATGTTCT | 114088 |
rs11620641 | snp | A/T | 0.382473 | 0.212016 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091814 | TTCAAGGGTTTTAAC[A/T]TTCTTTTGTGGCAGG | 114088 |
rs11620762 | snp | A/G | 0.103438 | 0.202533 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092105 | GTAGGGCAATTCAAC[A/G]TGGACTATAATTAGC | 114088 |
rs11620848 | snp | A/G | 0.397633 | 0.201754 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085139 | AATATTTGGTGCCAC[A/G]CAGTTACTTCTTAAA | 114088 |
rs11621274 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983230 | GGCATCTTTTCCATT[C/T]TTTAAGAGTTTGAGA | 114088 |
rs11621679 | snp | A/G | 0.251014 | 0.249998 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067931 | cagagaaagtcttgt[A/G]tattgttgtatgcca | 114088 |
rs11622035 | snp | C/G | 0.477004 | 0.104734 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055839 | ATGTACATTTTAGAA[C/G]CCATGAATACAATAT | 114088 |
rs11622225 | snp | G/T | 0.228253 | 0.249052 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047121 | TGCCTCTGCTTGAGC[G/T]GGGGTTGACACTTGT | 114088 |
rs11622355 | snp | A/G | 0.318896 | 0.240319 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073454 | tcataaaaatggaat[A/G]ccatacaacagtcag | 114088 |
rs11623697 | snp | A/C | 0.233235 | 0.249437 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081945 | caagagtttttatag[A/C]actcaatctccagcc | 114088 |
rs11623936 | snp | A/G | 0.193653 | 0.243567 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014854 | ACCCCTTGGCATCAC[A/G]TATGCAGTGGGCTGG | 114088 |
rs11623955 | snp | C/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011552 | CACATCCCCAATATT[C/T]ATACTACTTTGCAAA | 114088 |
rs11624451 | snp | A/G | 0.468249 | 0.121932 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057521 | GCTAAAATAAAAGAT[A/G]CTAAATTGAAAATAA | 114088 |
rs11625562 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975957 | TACTCCAGAAAATTA[A/G]GCTGTGAATGGCAGC | 114088 |
rs11626007 | snp | A/G | 0.382085 | 0.212258 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089114 | ACTGATGCTGAGAGT[A/G]AACTTAGTTTCTAGC | 114088 |
rs11626230 | snp | A/G | 0.228842 | 0.249103 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046531 | cagtcatctgaattc[A/G]aaaagAAAGAAACAC | 114088 |
rs11626271 | snp | A/G | 0.330714 | 0.236612 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988877 | GAGTCTTAGAGGGAA[A/G]AAACTTAATATCATC | 114088 |
rs11626550 | snp | A/G | 0.149999 | 0.229128 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006400 | TGAACGCCACAACAG[A/G]AAGAGTTGTGTATAT | 114088 |
rs11626717 | snp | C/T | 0.476833 | 0.105105 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055678 | TGTCTCCTAGAGCAT[C/T]CAGCTCTACTGACAC | 114088 |
rs11626757 | snp | C/T | 0.476918 | 0.104919 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055767 | GGATAAATTTGTGTT[C/T]GTTCAAGCTACTAAG | 114088 |
rs11626802 | snp | C/T | 0.227369 | 0.248974 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042148 | ACTCCCTCACTCCAG[C/T]ATGATGATGCATTAT | 114088 |
rs11627694 | snp | C/T | 0.0563993 | 0.158176 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977250 | TGTGGCTCTCGCAGG[C/T]GGAGGTAAGAACAGG | 114088 |
rs11628238 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060511 | ttgctctgtcgccca[A/G]gctggagtgcagtgg | 114088 |
rs11628407 | snp | A/G | 0.397633 | 0.201754 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083812 | AAAATGTGAACTTCT[A/G]ACATTTTGAAATACA | 114088 |
rs11628591 | snp | A/G | 0.310878 | 0.242475 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024049 | GCAATGCTAAATTTT[A/G]GCTTTCACGGCAATT | 114088 |
rs11628625 | snp | G/T | 0.429388 | 0.174127 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015156 | GATATGACACTGATA[G/T]CTACTGGTTAAAGGA | 114088 |
rs11844215 | snp | A/G | 0.350327 | 0.228986 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024930 | GTTTTGGAAACCTAC[A/G]AGGTTTTACAAGCTC | 114088 |
rs11844311 | snp | A/G | 0.227959 | 0.249026 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049296 | GTCTTATTTTGTTTT[A/G]CAGATTGAAAAGATT | 114088 |
rs11844329 | snp | C/T | 0.498714 | 0.0253268 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016019 | GGTCCGGTACAGTTG[C/T]CTCCTCAGTATCTGT | 114088 |
rs11844384 | snp | A/G | 0.4983 | 0.0291038 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019405 | TTAACTATAATTTAC[A/G]TTTCAAACAGTTTCC | 114088 |
rs11844527 | snp | C/G | 0.228253 | 0.249052 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049652 | CCAAAATGGTGAAAC[C/G]CCATCTCTACTAAAA | 114088 |
rs11844545 | snp | A/G | 0.252702 | 0.249985 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049950 | ggaggggttgggtgc[A/G]ttaagagtggaaaga | 114088 |
rs11844781 | snp | C/G | 0.334412 | 0.235318 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979639 | ACCAGTGTCTTGCAA[C/G]CTGTTTATAATCATC | 114088 |
rs11844823 | snp | G/T | 0.276432 | 0.248599 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979572 | AAAAGAGAAAAATTG[G/T]GGTTCATTTCCTTGT | 114088 |
rs11844864 | snp | G/T | 0.326506 | 0.238006 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979669 | CACTACCCCAAAACC[G/T]TTTCCCTAATCATCC | 114088 |
rs11845592 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992848 | GCCCACTTTTTAGAA[A/G]GCAGTTTTTAAGATG | 114088 |
rs11846120 | snp | A/G | 0.353371 | 0.227628 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068979 | CATTTGGCAGTGATT[A/G]GTCTGATAGAATATA | 114088 |
rs11846226 | snp | A/G | 0.191775 | 0.243125 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004086 | AAGGAAGAGCATTGT[A/G]TTTTACTGGAACTCC | 114088 |
rs11847331 | snp | C/T | 0.192088 | 0.2432 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003033 | GTCTTGCTCACTAAA[C/T]AAACTACAGGACTGG | 114088 |
rs11847412 | snp | A/G | 0.0356815 | 0.128715 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974903 | gctacccgggaggct[A/G]aggcaggagaattgc | 114088 |
rs11847472 | snp | A/G | 0.244776 | 0.249945 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040116 | CAGGATAAAGTATAT[A/G]CGGATAAAGTCTCTT | 114088 |
rs11848207 | snp | C/T | 0.236957 | 0.26785 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076160 | CACAGATGAGGAAAC[C/T]GAGGTACAGATGGGA | 114088 |
rs11848681 | snp | C/T | 0.490267 | 0.0690764 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025238 | ATTAACCGGCGGGTT[C/T]CCTTGCGTCCCAGGT | 114088 |
rs11849278 | snp | C/T | 0.229723 | 0.249176 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037702 | GACACAGAGACTCTT[C/T]GGCTCTTTAAAAAAA | 114088 |
rs11850318 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038358 | aaaaaatctatgttg[A/T]tttaagttgctaagt | 114088 |
rs11850410 | snp | A/C | 0.224412 | 0.248687 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047751 | ACCCAATGCTATGGG[A/C]AATGCACCTTAGAAA | 114088 |
rs11851076 | snp | C/T | 0.192088 | 0.2432 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002778 | AAGCCGGTCAATTGT[C/T]GTATACTTAAGAAAA | 114088 |
rs11851596 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018736 | AGCCCTCAGCATCCT[C/T]GCTGAGTAATTTTGT | 114088 |
rs11852198 | snp | C/T | 0.0298908 | 0.118541 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996507 | TAGAAATAGTTTTCC[C/T]GCAGATCTGATAACA | 114088 |
rs12100459 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082877 | TCTTCTGTGCAGTAA[C/T]GGCAGgtatagtggt | 114088 |
rs12101017 | snp | G/T | 0.17654 | 0.238964 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062511 | tagatatttgaaaac[G/T]atttgaaggcattgg | 114088 |
rs12101171 | snp | C/T | 0.100588 | 0.200439 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002767 | ATGAGAAGGTGAAGC[C/T]GGTCAATTGTCGTAT | 114088 |
rs12147026 | snp | C/T | 0.422473 | 0.180978 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050030 | aattttggaagtaaa[C/T]gatgcagagccgtga | 114088 |
rs12147541 | snp | C/T | 0.432504 | 0.170857 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040504 | GAGAAGTGGCAATTC[C/T]TCAGAGGGATCAGGA | 114088 |
rs12147963 | snp | G/T | 0.159292 | 0.232964 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070111 | cattttggtgctttt[G/T]ggtggtgcatttgct | 114088 |
rs12184968 | snp | C/T | 0.287085 | 0.247234 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071811 | ccctgtctcaaaaaa[C/T]aaataaaTGAATAAT | 114088 |
rs12323589 | snp | A/C | 0.28578 | 0.247426 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999541 | GAATTGTAGAAGACA[A/C]GGCCCCTGCTCTCAA | 114088 |
rs12431591 | snp | A/G | 0.465788 | 0.126237 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054963 | gcctcctgagtagct[A/G]ggacaacaagcgcgc | 114088 |
rs12431974 | snp | C/T | 0.392881 | 0.205147 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993357 | GCTGGAACGCTACTC[C/T]TTTCAACAAGACTCT | 114088 |
rs12432099 | snp | C/T | 0.495634 | 0.0465208 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028721 | GTTACTGAAAAGGTG[C/T]CACGATCTGAAGGTG | 114088 |
rs12432414 | snp | C/G | 0.312348 | 0.242101 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093053 | GTCGTTTGAGGAACA[C/G]TAAGAAGCAGTGTGG | 114088 |
rs12432432 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992417 | ACCCTGTCTCTACGG[A/G]AAAAAAAAAAAGCCA | 114088 |
rs12433567 | snp | C/T | 0.436692 | 0.166271 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074836 | AACAGGGCTGTGGAG[C/T]CCCCAGGGCACTTCC | 114088 |
rs12433809 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030610 | gtgtatgagtgtgca[C/T]atgcctgtgagtgtg | 114088 |
rs12433833 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030698 | GAATGTGTATGTGTA[C/T]GTATGTGATTGTATG | 114088 |
rs12434043 | snp | C/T | 0.227664 | 0.249 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048358 | CCACATTCATTGTGA[C/T]GGTCTAGGAAAAGAC | 114088 |
rs12434077 | snp | G/T | 0.227664 | 0.249 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048521 | TTGGTTAATTACTAG[G/T]GACATAAAGGCCAAT | 114088 |
rs12434118 | snp | C/G | 0.439918 | 0.162576 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999863 | AAGCTCTGTATGAGA[C/G]AAGCAGACACATGCC | 114088 |
rs12434339 | snp | C/T | 0.330249 | 0.23677 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987594 | TGAATGACTTAATAT[C/T]ATGTATTATCATTTC | 114088 |
rs12434376 | snp | C/T | 0.330249 | 0.23677 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987743 | GTTTCTATTATGGAG[C/T]GAAGGCATTTACAAC | 114088 |
rs12434377 | snp | A/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987784 | TCaataaaatatttt[A/T]tttatttatttattt | 114088 |
rs12434983 | snp | A/G | 0.454664 | 0.143571 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028803 | TTCTTGGCTGGGAGC[A/G]TGCTGAGAATCACCG | 114088 |
rs12435217 | snp | C/G | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046303 | cttacacaggtgata[C/G]aatcattttgaactc | 114088 |
rs12435402 | snp | C/T | 0.338523 | 0.233803 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071259 | CACATGCCTGTAATC[C/T]CAGCTACTCTGGAGG | 114088 |
rs12436365 | snp | A/G | 0.492775 | 0.059668 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095863 | CATTAGTCAGAATCT[A/G]TGACCCCTTCGTTTC | 114088 |
rs12436641 | snp | A/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090966 | GAATGTGAACTGCTT[A/T]AAATCACAAAGTAAT | 114088 |
rs12436728 | snp | A/T | 0.397271 | 0.202018 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084141 | TTATATCTAAATGTC[A/T]AGAGCTTACTATCAG | 114088 |
rs12586141 | snp | A/C | 0.103794 | 0.20279 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091795 | TAGCCTACTTATGTC[A/C]TGTTTCAAGGGTTTT | 114088 |
rs12586732 | snp | G/T | 0.434831 | 0.168337 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994041 | CAGAGGTGATTACAT[G/T]AAGGATCTTGAGATG | 114088 |
rs12588085 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053519 | GTATTCTTTTTTTTT[C/T]TTTTTTTTTTATGCG | 114088 |
rs12588888 | snp | A/G | 0.400325 | 0.199756 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058479 | AGCTCCTCTTCAGCT[A/G]GGTGTGGCCCTGAAA | 114088 |
rs12588907 | snp | A/C | 0.39979 | 0.200158 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058456 | CCAGAATAAAGACTG[A/C]ATTTCTTAGCTCCTC | 114088 |
rs12588959 | snp | A/G | 0.293294 | 0.246223 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058561 | AGGCCATACCCTCCC[A/G]TCATCTGTTCCCACT | 114088 |
rs12589524 | snp | A/G | 0.455502 | 0.142369 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001347 | CCATTCTCCTGCCTC[A/G]GCCTCCGGAGTAGCT | 114088 |
rs12590216 | snp | C/T | 0.184521 | 0.241273 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002335 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAAGATG | 114088 |
rs12879906 | snp | A/G | 0.133777 | 0.221342 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975912 | TAGTAATGACATACA[A/G]TCCCATGTTTTTCCA | 114088 |
rs12881774 | snp | A/G | 0.111928 | 0.208413 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994054 | ATTAAGGATCTTGAG[A/G]TGGGGGGATTATACT | 114088 |
rs12881920 | snp | C/T | 0.139225 | 0.224118 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992171 | GATGGGCTGAGGTGT[C/T]CCCTGTAGTTGTTCT | 114088 |
rs12882222 | snp | C/G | 0.132066 | 0.220435 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009786 | CTCTTAGCCAGTTTA[C/G]TAGAGTGTGACTTGG | 114088 |
rs12883270 | snp | A/C | 0.273856 | 0.248859 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997365 | TTGTATGGTGGCTCT[A/C]GGTAGCCTAGCCAAG | 114088 |
rs12887314 | snp | C/G | 0.45574 | 0.142025 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002146 | CTTTTTTTTGAGACG[C/G]AGTCTCGCTCTGTCG | 114088 |
rs12888385 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068760 | ATGAGGCCAGCCCAT[A/G]TTGCAGAACCAAGGT | 114088 |
rs12889589 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077387 | TCATCTCCAATTCTG[G/T]ttttttttttttttt | 114088 |
rs12891180 | snp | A/T | 0.473451 | 0.112115 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998919 | AAAGCACAGCCTTAA[A/T]ATGACAACTCTCTGG | 114088 |
rs12891408 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021387 | TGAGGTACTCTGTGA[C/T]CGTTTTAACTGCAAG | 114088 |
rs12891562 | snp | A/C | 0.277778 | 0.248452 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002267 | GCTGGGACTACAGGC[A/C]CCTGCCACCACGGCT | 114088 |
rs12891686 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072634 | ATTACTTTCTTGAGG[G/T]TATTGAGTTTCAATT | 114088 |
rs12892749 | snp | A/G | 0.195837 | 0.244062 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011507 | TGAAGCGTAAAATTG[A/G]AGAAGGGTTTTCCAG | 114088 |
rs12893276 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053628 | atactctaagtttta[A/G]ggtacatgtgcacat | 114088 |
rs12893822 | snp | A/G | 0.2462 | 0.249971 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012110 | CTGTAACCATTTTCA[A/G]GTGTGTAATTCCGTG | 114088 |
rs12894623 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018472 | TATGCCAATAATATC[C/T]GTAACGTAAATTTGT | 114088 |
rs12894786 | snp | A/G | 0.140581 | 0.224783 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975053 | TGGAAGCAGACCCCA[A/G]ACATCTCCACTGGAC | 114088 |
rs12895611 | snp | G/T | 0.112631 | 0.208878 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999682 | GCCTCATCCTCACGG[G/T]CCTGAGGTTTTTTTA | 114088 |
rs12896703 | snp | A/G | 0.23031 | 0.249223 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096916 | AATTGAATTGTAATG[A/G]AAGTTAATTATTGAG | 114088 |
rs12896768 | snp | C/T | 0.498253 | 0.0295011 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019064 | GAAGAAAGCATAGAT[C/T]TCATTAATGGCACAA | 114088 |
rs12896981 | snp | A/G | 0.465892 | 0.126058 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978893 | TAATAAATAATAATT[A/G]ACTAAGTTGTAGGTA | 114088 |
rs12897358 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075399 | GCCTGTTAGTAACTC[G/T]TCGGTGTACTGGAAT | 114088 |
rs17092860 | snp | A/G | 0.457853 | 0.138915 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978200 | TACTGCACATACTGA[A/G]ACACAACAATGAATT | 114088 |
rs17123302 | snp | C/T | 0.122411 | 0.214991 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975227 | AGGTGAATTGTCATC[C/T]GCAATAGATAAAAAC | 114088 |
rs17123305 | snp | C/T | 0.0333695 | 0.124785 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975773 | ATTTAGACAACTAAT[C/T]AGAACTTCTTTCCGG | 114088 |
rs17123312 | snp | C/T | 0.0729998 | 0.176553 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977847 | TATTTTACCAATTTC[C/T]GTGTATCCCCAAACC | 114088 |
rs17123314 | snp | G/T | 0.00131599 | 0.0256176 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979336 | GGCCCTGGGCAGCCT[G/T]TGAACCGGTAGCCAG | 114088 |
rs17123325 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980304 | CAAAGAATTGTGTCT[C/T]ATGCTTCAATTGATG | 114088 |
rs17123330 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984084 | AACCATCTCCCTTCC[C/T]TAAGATTTGGATACC | 114088 |
rs17123339 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987063 | CAGAGGTGGATCTTT[C/T]GCCAATTGAAGCCTT | 114088 |
rs17123344 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989755 | GACGGGACTGTGTTC[A/G]TAACGAATACGTATC | 114088 |
rs17123345 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990408 | GCCGTTGGGAAACAT[A/G]AAGTTGGCAGGAGAC | 114088 |
rs17123347 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990626 | GCAAACAGATTGTGG[C/T]TGCTTATGATAGTGT | 114088 |
rs17123356 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992275 | TGCTGGACCAAAATC[A/G]CTATTAAATATGAGC | 114088 |
rs17123361 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992885 | CAAGAATCCCAACCT[A/G]TTTGTCATTAGATAA | 114088 |
rs17123369 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995952 | CTATTGTTACAGATC[A/G]ATCATATCTTTTTTT | 114088 |
rs17123377 | snp | A/G | 0.146314 | 0.227484 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997554 | GGCCCTCTCTAAACA[A/G]CTCTAGCACCCCACC | 114088 |
rs17123379 | snp | C/T | 0.187685 | 0.242109 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998573 | GTACAGTATATAGCC[C/T]CTACTGAGCTCCTTA | 114088 |
rs17123383 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999330 | AAGGCAAAGTCAGGA[A/G]TGAGAAACTGACAAA | 114088 |
rs17123388 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999748 | CCTCAGTCCCCAGAA[C/T]GGCTGCTCCCTTAGG | 114088 |
rs17123391 | snp | C/G | 0.0955749 | 0.196603 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001594 | TTAATAAACCAGAGA[C/G]TGCCTATTCTGAGAA | 114088 |
rs17123409 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004304 | ATTCTCACTGACTTC[C/T]TTGAAGAGGTCTGGC | 114088 |
rs17123411 | snp | C/G | 0.446118 | 0.155041 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004315 | CTTCCTTGAAGAGGT[C/G]TGGCGGAGCTGTGGT | 114088 |
rs17123421 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005792 | TTCTAATCAAAATAC[A/T]ACCAGAAAACGTGCC | 114088 |
rs17123439 | snp | C/T | 0.126669 | 0.217462 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009274 | CTAAGAAATACACCA[C/T]CACACTTGAAACACA | 114088 |
rs17123448 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010170 | AAAAAGCCCATGGAC[C/T]TCTCAGACTTGTAGT | 114088 |
rs17123456 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011015 | ATTGTTCTGCATCTT[C/T]TTCCTTGCGTGGATG | 114088 |
rs17123477 | snp | C/T | 0.463666 | 0.129795 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011905 | AGGCAGTTTTCATGT[C/T]GCCACAACCAATGGT | 114088 |
rs17123479 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013738 | CACCACCATATGTTG[A/G]TCTGGGCTCAATGAA | 114088 |
rs17123480 | snp | C/G | 0.117537 | 0.212022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014703 | ATCTTCTTCAACTTG[C/G]GTTACTCATACCACA | 114088 |
rs17123481 | snp | G/T | 0.0663309 | 0.169604 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014883 | GGATTCAAGAGGTCC[G/T]TTTCTCAGGGACAGG | 114088 |
rs17123489 | snp | G/T | 0.493154 | 0.0581045 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015381 | TTAGGAGAATTTCAT[G/T]CTTAACCCAACCATG | 114088 |
rs17123497 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016013 | GTTTAAGGTCCGGTA[C/T]AGTTGTCTCCTCAGT | 114088 |
rs17723941 | snp | A/C | 0.0809363 | 0.184167 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003706 | TGTCCCAGATTTAGA[A/C]AAATTAGCAAATGGA | 114088 |
rs17724183 | snp | G/T | 0.197703 | 0.244469 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008012 | TTTAAAGCACTGAAT[G/T]CTAAGAGTCATTTAC | 114088 |
rs17796080 | snp | C/T | 0.307176 | 0.243374 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980951 | AATGTCTGACTTGCT[C/T]TCCCTTTGATCTGGT | 114088 |
rs17796541 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993828 | TGTGCTGAGCATTGG[C/T]GGCTTAAAGTCCTGG | 114088 |
rs17796553 | snp | A/G | 0.111928 | 0.208413 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994880 | TTACAGTTATATTTC[A/G]TCTTAAGTCAGTGTA | 114088 |
rs17796649 | snp | C/G | 0.0275645 | 0.114116 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996656 | GTTGCATCTAGGAAA[C/G]ACTCTTGGAGGGCTT | 114088 |
rs17802253 | snp | G/T | 0.215144 | 0.247558 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999766 | CTGCTCCCTTAGGAA[G/T]CTCCAAGCATCAGAA | 114088 |
rs17802296 | snp | A/G | 0.201418 | 0.245234 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000169 | ACATTAGAAGCTGTG[A/G]ATTGCAGAAATAAAT | 114088 |
rs17802520 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005147 | TGAGTCCATGCATTT[C/T]AGGCTATCAGCATTA | 114088 |
rs17803300 | snp | A/G | 0.190833 | 0.242898 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024691 | TATAGTTGCCAGGGG[A/G]TCATGGTTGAAAAAT | 114088 |
rs17803330 | snp | C/T | 0.188946 | 0.24243 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024738 | AGAGGAGAAGCATTA[C/T]TGTGGGTCAGGGAGG | 114088 |
rs28409499 | snp | C/G | 0.132066 | 0.220435 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059856 | AAACAAAACAAAACT[C/G]TGCTCTATTCTTCTA | 114088 |
rs28441253 | snp | C/T | 0.247905 | 0.249991 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018575 | TAACAAAGATAATGG[C/T]GAAAAGAATGATAAT | 114088 |
rs28465677 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051737 | TTTGGGAGGCTGAGG[C/T]GGGTAGATCACTTGA | 114088 |
rs28487585 | snp | C/G | 0.263535 | 0.249633 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043325 | GGCAGCTGAGACATG[C/G]AGCCGGAGGAAGGAG | 114088 |
rs28504356 | snp | C/T | 0.499598 | 0.0141716 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983156 | AAAGAGTGCTTTGCA[C/T]TGATGTAAAAGAAAA | 114088 |
rs28627581 | snp | C/T | 0.397633 | 0.201754 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083120 | AATATAACAGATTCC[C/T]ACATCTTGCTTCCTT | 114088 |
rs28631468 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090848 | GAGATCTGACCGCCT[C/T]GGCCTCCCAAAGTGC | 114088 |
rs28642840 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047042 | CTTTGAGGATGGGGA[C/T]GGGGATACATGGAGT | 114088 |
rs28656870 | snp | C/T | 0.115088 | 0.210473 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067336 | AACCTTAGTCCTAGC[C/T]ACCATCACCTCTCTC | 114088 |
rs28672773 | snp | A/G | 0.121022 | 0.21416 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033322 | GGTCTTGAACTCCTG[A/G]CCTTGTGATCTACCT | 114088 |
rs28677862 | snp | A/G | 0.263535 | 0.249633 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043309 | GGCCTTGAGAGCAGA[A/G]GGCAGCTGAGACATG | 114088 |
rs28681426 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078187 | AAACACAGATCTAAA[C/T]TCTTTAACATGGTTG | 114088 |
rs28683704 | snp | G/T | 0.397452 | 0.201886 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085144 | TTGGTGCCACACAGT[G/T]ACTTCTTAAAGTGCA | 114088 |
rs28687451 | snp | A/C | 0.216649 | 0.247765 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084868 | TTATGTCATAGAGTA[A/C]TTTGGCTTTGGATGA | 114088 |
rs28715723 | snp | A/G | 0.248471 | 0.249995 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990977 | TAATTTATAATAAAA[A/G]GTGGTATTTTAAGCT | 114088 |
rs33936825 | in-del | -/CACACAGGTGTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025418 | TACACCAACAAGGCC[-/CACACAGGTGTTTT]AGCGAGACTCAAAAC | 114088 |
rs34016133 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067841 | TCACAGCACCAGCCC[-/C]TTACCTGAAAATCTA | 114088 |
rs34019183 | in-del | -/T | 0.375 | 0.216506 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001247 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTGTCGC | 114088 |
rs34029108 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081250 | CACATGAAAAGATTC[-/C]TCAACATCACTAGTC | 114088 |
rs34041338 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003317 | GGGGTATTTATTCTT[-/T]AACTGTCCTTATTAG | 114088 |
rs34062978 | in-del | -/ACAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080437 | ATTGAGTTTTATTGA[-/ACAC]ACACACACACACACA | 114088 |
rs34137743 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094412 | CATGACGGTGGCTTC[-/C]TTGGGCGCCTTCTCG | 114088 |
rs34143086 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018294 | CTGCCTGCCTTCCTT[C/T]CTTCCTTCCCTCCTC | 114088 |
rs34153026 | snp | C/T | 0.44858 | 0.151875 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998333 | TATTGGGCCATTTAA[C/T]TTACCTTTTTAGCCT | 114088 |
rs34158603 | snp | C/T | 0.100231 | 0.200173 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026854 | AAAAGGTGGGAAGAA[C/T]AGTAATACTTTGTAG | 114088 |
rs34163607 | snp | C/T | 0.179744 | 0.239925 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040173 | AAGTAAATATTTCCT[C/T]GGATGGTCTTATATT | 114088 |
rs34171875 | in-del | -/T | 0.32885 | 0.23724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039755 | AAACTTTTTTTTTTT[-/T]GAGGCGGAGTCTCTC | 114088 |
rs34201811 | in-del | -/T | 0.401424 | 0.198924 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084174 | CAAACTTTTCCACAC[-/T]TTTTTTTTATATATA | 114088 |
rs34237668 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018649 | GCATTCTACAGATAG[C/G]TACAATGGGCACACG | 114088 |
rs34267736 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063019 | AAAATCAAGCAACAG[-/C]AAACACCCTGAGATG | 114088 |
rs34269881 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035157 | CAAAGGATACACATT[-/T]AAGGGTTAATTATCA | 114088 |
rs34285851 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093517 | TGCCCTCTCCGCTCT[C/G]TCTTTTGAGCACGTG | 114088 |
rs34288227 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027445 | CACCGTGCCCAACCA[C/G]CTGTTAACTCTTATT | 114088 |
rs34298749 | in-del | -/A | 0.0298908 | 0.118541 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003647 | AAGGATAAAAAAAAA[-/A]GGCTAGACTCTCAAT | 114088 |
rs34335283 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042197 | CAAAGCCGTTGCAAG[-/G]TATGTGACAGAAATC | 114088 |
rs34373063 | in-del | -/AT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025760 | GCTATTGGTCTGGGT[-/AT]AGGGCAGAAAGAATA | 114088 |
rs34385009 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047200 | ATTCTGTCCCTTTTT[-/T]CCTAGAATTCCCTTT | 114088 |
rs34385335 | in-del | -/A | 0.0190104 | 0.0956233 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080537 | CTTAATGTAAATAAT[-/A]AAAAAAAGGGGTCTT | 114088 |
rs34404791 | in-del | -/A | 0.463451 | 0.130149 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047960 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAT | 114088 |
rs34469615 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995961 | CATATCTTTTTTTTT[-/T]AAAATAAGCTATTCA | 114088 |
rs34525509 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053160 | CAAAAAAAAAAAAAA[-/A]GAGAAGAAAACTTGT | 114088 |
rs34547542 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017044 | TGTGAATTAAAGGGG[-/G]AAGTGCTTTGGCTGT | 114088 |
rs34560711 | in-del | -/T | 0.0287284 | 0.116357 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980981 | TTGAACACTACTGTA[-/T]TTTTTTTTTTTTTCA | 114088 |
rs34561390 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093327 | AAGGGCTTGAATTCC[-/C]GGAGAAGTGGGTGTG | 114088 |
rs34610151 | snp | C/T | 0.121369 | 0.214369 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000309 | ATTATCTAATGGACT[C/T]TTAGCAACAAAGCAT | 114088 |
rs34629152 | in-del | -/AC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080437 | ATTGAGTTTTATTGA[-/AC]ACACACACACACACA | 114088 |
rs34631387 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999763 | CGGCTGCTCCCTTAG[-/G]AAGCTCCAAGCATCA | 114088 |
rs34653117 | in-del | -/TTAT | 0.240765 | 0.249829 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062103 | AGTCCAATAAATAAA[-/TTAT]TTATTTATGATATTG | 114088 |
rs34673300 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073002 | ATTTATTTTTTTTTT[-/T]GGCAACTCAATGGAA | 114088 |
rs34678449 | snp | A/G | 0.144632 | 0.226711 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015445 | TCCATTTTACATGTG[A/G]TTCTTTTAAAATTTT | 114088 |
rs34748194 | in-del | -/AACA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005558 | ATCTATTCTCAACCA[-/AACA]GTAAAGCCCTTGGCT | 114088 |
rs34835418 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072145 | TGCCAGAGCCTTCAG[A/G]AGGTTCCAGGAATAG | 114088 |
rs34861546 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028422 | ATTTTAATCACATTT[-/T]ATAAGCTCCATCTGA | 114088 |
rs34871706 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040679 | ATGCCCTAAGTTTTT[-/T]AAGAACTTGTGTGTA | 114088 |
rs34881612 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069490 | GAATTGCCCATCCCC[-/C]AAATGTCAACAGTGC | 114088 |
rs34908932 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071456 | AGACTTCACTTGAAA[-/A]TGCCAACTCTGATAC | 114088 |
rs34915549 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087950 | TATTACATTAATATT[-/G]CCTCATGCCTAAAAT | 114088 |
rs34926668 | in-del | -/GT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030586 | ATGAGTGTGCATATG[-/GT]GTGTGTGTGTGTATG | 114088 |
rs34933389 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083441 | AAAAATTTTTTTTTT[-/T]AGAGATCAGGTCTCA | 114088 |
rs34951104 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070121 | TTTTTGGTGGTGCAT[-/C]TTGCTGTTTAAATGG | 114088 |
rs34986653 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046172 | GTGATGGGGTGGGGG[-/G]TTGAACCAGGTTGGG | 114088 |
rs35045316 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975840 | ATTTCAAGGGTAACC[-/C]TATGTAAGTCTATCT | 114088 |
rs35090699 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034356 | GAAGTTTTTGAAAAA[-/A]GGGTCCCTTCTCCTC | 114088 |
rs35163876 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018143 | GAATAACTGAGTTCT[-/A]TTGTCATTAATTTTA | 114088 |
rs35194958 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093354 | TGTGTGTATAGTTGG[-/G]AGGAGAAGGTTTCCC | 114088 |
rs35207253 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089944 | ATTTACCTTATCAAA[-/A]TCCTTTCACAATTGT | 114088 |
rs35214711 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001138 | TTGAAGACATTATCC[-/C]TAAAGGAAATGTTTT | 114088 |
rs35217074 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079657 | AGGTATAATTCAAGG[-/G]AACTGTCAGCACTGG | 114088 |
rs35270363 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51084516 | ATTTCCTTGCTAAGT[-/A]CTTGGCTAGATGACT | 114088 |
rs35280356 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056810 | TCTCTATCATTGCTG[G/T]CTTGTCACACAAATA | 114088 |
rs35285847 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083586 | GCAGCATTCTTCACA[C/T]GTCTGTGGAGTTAAG | 114088 |
rs35340936 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027447 | CCGTGCCCAACCAGC[G/T]GTTAACTCTTATTTG | 114088 |
rs35357166 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007029 | ACCGTGAGCAGATGG[-/G]ACATGACTCAGGAGG | 114088 |
rs35445652 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50986335 | CAGATCAGGACCCAA[-/A]GACCAGAGGACACCT | 114088 |
rs35511164 | snp | G/T | 0.493386 | 0.0571263 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015162 | ACACTGATATCTACT[G/T]GTTAAAGGAGAGTCT | 114088 |
rs35537613 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016148 | CCTCTTATATACTTT[-/T]AAATCATCTCTAGAT | 114088 |
rs35578096 | in-del | -/C | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974994 | ACAGAGTGAGATTCC[-/C]GTCTAAAAAAAAAAA | 114088 |
rs35591350 | in-del | -/GG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994061 | TCTTGAGATGGGGGG[-/GG]ATTATACTGGATTAT | 114088 |
rs35634335 | in-del | -/TCA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001734 | TTTGGATCCAAGTGA[-/TCA]GATCACAGTGATCTC | 114088 |
rs35634487 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013487 | ATTTGTCCTTCTTTT[-/T]CAAGATTGTTTATTT | 114088 |
rs35659590 | in-del | -/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993385 | CTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCAC | 114088 |
rs35678882 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055305 | TTACAAGATATATCC[-/C]TTGTATTCCACATTG | 114088 |
rs35681416 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056700 | CTTAGGCCATTATCC[-/C]TTACTCCCAGTTTCA | 114088 |
rs35727332 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095774 | TGCGTCCCTCGTTTC[-/C]TAAAGAGCATGTATA | 114088 |
rs35728859 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076452 | CCCACATGTGAGGGG[-/G]AAGCAGCCATAAGCA | 114088 |
rs35745283 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976124 | CACTCTTTTTTTTTT[-/T]CAACTGTCAATTTTT | 114088 |
rs35751941 | in-del | -/T | 0.326035 | 0.238157 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079511 | TTTCAAAAGAAAAGA[-/T]ATTATGTGAGTGCAT | 114088 |
rs35783894 | in-del | -/A/AA/AAA | 0.456685 | 0.140646 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031165 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GAAAGAAAAGAAAAG | 114088 |
rs35804116 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018790 | ACATGGAAACTGAAA[-/A]GCTAGAATTTTTCCC | 114088 |
rs35809678 | snp | C/T | 0.189576 | 0.242588 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024226 | TCTGATGAAGAGGCC[C/T]GGGCAGAGGCAAGCC | 114088 |
rs35834822 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053464 | ACACTCTGAGAATGT[C/T]TCAGACACACAAGCT | 114088 |
rs35852938 | snp | A/C | 0.190519 | 0.242821 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022068 | CATCCTCTTTTCCTA[A/C]TTTTAGAATTTTTCT | 114088 |
rs35856104 | in-del | -/A | 0.330482 | 0.236691 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992417 | ACCCTGTCTCTACGG[-/A]AAAAAAAAAAAGCCA | 114088 |
rs35880725 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984151 | TGCCTAGTCTTAAAA[-/A]TGTTCAAAAGTGTGT | 114088 |
rs35882115 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060389 | TATTTATACAACCAC[A/G]CAGTATGTATTCTGT | 114088 |
rs35902015 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039321 | GATAGCATATGTCCA[C/T]GAAAGACTTGCATAC | 114088 |
rs35902557 | in-del | -/G | 0.0923359 | 0.194016 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002125 | TGTGTGTGTGTGTGT[-/G]TTTTTCTTTTTTTTG | 114088 |
rs35907683 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027885 | GGACTACCATAGTTT[-/T]CTTCCTCTTTTTATT | 114088 |
rs35929206 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051559 | GGAAGAGATGCATTT[-/T]ATATAGCTTGCTATT | 114088 |
rs35938666 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018109 | GTGCCTAATTTTTCC[-/C]AAATGTCTTCATTGT | 114088 |
rs35996765 | snp | A/C | 0.0912534 | 0.193131 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014783 | TGGAAGCCAGGCCAC[A/C]TCACTGTTGTCTTTG | 114088 |
rs36012437 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984405 | AATATAAAAATTATG[-/C]ATCTTACTTTTGGTT | 114088 |
rs36025277 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075258 | GCTATTCTAGGTTCC[-/C]TTGATGGAGCCCCAC | 114088 |
rs36029319 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51009972 | AGGTGTCAAGAAGGT[-/G]AGACATCTTACAAAC | 114088 |
rs36055641 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027446 | ACCGTGCCCAACCAG[-/C]TGTTAACTCTTATTT | 114088 |
rs36070860 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080718 | TGGAAGTGACTTTTT[-/T]GAATACTGCCATGGT | 114088 |
rs36090116 | snp | C/T | 0.0131567 | 0.0800327 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981934 | TCGCTATGACAACCA[C/T]CCTGATCCTGCCTTT | 114088 |
rs36204061 | in-del | -/AGAAG | 0.381308 | 0.21274 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052043 | GGGAGGGGAGGGAAA[-/AGAAG]AGAAGAGAAGAGAAG | 114088 |
rs36207618 | in-del | -/AAGAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052060 | AAGAGAAGAGAAGAG[-/AAGAG]GAGAAGAGAAGAGAG | 114088 |
rs41299203 | snp | C/T | 0.093777 | 0.195178 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998241 | CCCCCTTCTGAGGGG[C/T]GAGGGAGGCAGTGTC | 114088 |
rs45498595 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977213 | AACTCTGCACCCCAC[C/G]ACGGCTGGCTGAGCT | 114088 |
rs55679457 | snp | A/T | 0.487871 | 0.076925 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081377 | TGTGGAGAAATTCGA[A/T]CACTCATACACTGCT | 114088 |
rs55681440 | snp | C/T | 0.357877 | 0.225527 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075461 | CATTTGAAAATTATA[C/T]ACCAAAGATTTGTCT | 114088 |
rs55696069 | snp | C/T | 0.397633 | 0.201754 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086452 | TTTAATGATTACTGT[C/T]AGGCTAATTTGAGAA | 114088 |
rs55743214 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028181 | ATCAATTTATTTCCA[A/T]TTTCCTCTTTGTGTT | 114088 |
rs55769522 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015181 | AAAGGAGAGTCTGAA[A/G]GACTGTTGTGTCTCT | 114088 |
rs55801251 | snp | A/G | 0.323197 | 0.239044 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038868 | AAGTGGCTATGGTTC[A/G]GTTCAGAAGCCTAAA | 114088 |
rs55802293 | in-del | -/AG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060702 | CGATCTACTGACCTC[-/AG]GTGATCTGCCCGCCT | 114088 |
rs55842407 | snp | A/C | 0.291493 | 0.246533 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071955 | TACGCATTTGCCAAT[A/C]CCGGACTCAGCAGCG | 114088 |
rs55852741 | snp | A/G | 0.241053 | 0.24984 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060980 | TTTTCATTTTAATAA[A/G]TTATATAAAATGGCA | 114088 |
rs55873582 | snp | C/T | 0.112983 | 0.209108 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995216 | AATTAATTTTTATTG[C/T]TTTCCTAATTCTCCT | 114088 |
rs55925248 | snp | A/G | 0.241053 | 0.24984 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060847 | GTATTGCTGAATAGT[A/G]TTCCATTAACTTTAT | 114088 |
rs55928212 | snp | A/G | 0.325799 | 0.238232 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076721 | TTCATCTTCGCAACA[A/G]TCCTTGGTGAATGGT | 114088 |
rs56022421 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060681 | GCCGTGTTAGCCAGG[A/C]TGGTCTCGATCTACT | 114088 |
rs56122519 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065433 | AGTCCAGGAAGTGCA[A/C]TGTATGGGGCAGTCA | 114088 |
rs56158068 | snp | A/G | 0.0744748 | 0.178019 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977910 | TTTCATGCAGTTCTT[A/G]TCCCTGTCTTCTCCA | 114088 |
rs56170539 | in-del | -/TT | 0.439502 | 0.163061 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978758 | TTTATCTGTTTTTTT[-/TT]GTTTTTTTTTTTCAC | 114088 |
rs56228903 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025871 | GGCAGGATGACATTC[C/T]ACTCCTGCCTCATCC | 114088 |
rs56257001 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065452 | ATGGGGCAGTCACAA[C/T]ATGTCATCTTCCAGC | 114088 |
rs56283868 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060701 | CTCGATCTACTGACC[G/T]CGTGATCTGCCCGCC | 114088 |
rs56294464 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052130 | TTAGGGTCTTTTATA[G/T]GACAGGCACAATGAT | 114088 |
rs56312729 | snp | C/T | 0.227369 | 0.248974 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042425 | CCATTCTCCTTTCAG[C/T]GAAATTCACTCACAT | 114088 |
rs56408541 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015354 | ACAACCAGAAGCAAG[A/C]CCTGAGGTTAATTAG | 114088 |
rs56726763 | in-del | -/AA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071402 | GAAAAAAAAAAAAAA[-/AA]GACAAGACAAAAGAA | 114088 |
rs56981170 | in-del | -/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096293 | AAGGAAGGGGGGGGG[-/G]AAAGGAAAGGCGGAA | 114088 |
rs56981237 | snp | A/G | 0.0271762 | 0.113356 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979143 | ATTAGCCAACCATGA[A/G]GAGAATTCTAGTTTC | 114088 |
rs57023283 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044113 | TTTAAAAAATTTGCA[C/T]AAGTACTAGACTGTA | 114088 |
rs57050947 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062303 | CATCTTTGGGCATGC[C/T]GTGTAGACTGCTTTG | 114088 |
rs57092161 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037441 | AACAAAAACAAAAAC[A/C]AAAACAAAAAACCTC | 114088 |
rs57305071 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015024 | CAGTTTCAGAGAAGG[C/T]TTTTAAAATTTTATC | 114088 |
rs57454311 | snp | C/T | 0.191775 | 0.243125 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004101 | GTTTTACTGGAACTC[C/T]TGTTATTGGGGCTGT | 114088 |
rs57535388 | snp | A/G | 0.437824 | 0.164991 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081731 | ATAATTCACTAGAAT[A/G]ACTCACAGAACTCAG | 114088 |
rs57541207 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062404 | ACTGCACTGTAAAGA[A/G]CAATAAAAGTACCAG | 114088 |
rs57641520 | snp | A/G | 0.46875 | 0.121031 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060553 | CTGACTGCAAGCTCC[A/G]CTTCCAGGGTTCACA | 114088 |
rs57676780 | snp | C/T | 0.275999 | 0.248644 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090241 | TGCTGCCTGTTACAT[C/T]TACCACAGGAATATA | 114088 |
rs58066729 | snp | A/G | 0.046775 | 0.145601 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082447 | ATAAAAAAGAATGAT[A/G]TACTGAGGCATGCTA | 114088 |
rs58136389 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065611 | AGACAGTGTAACTGC[C/T]GAGTTGAGATGAAGG | 114088 |
rs58170601 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012839 | TTTTCATACGTTTAT[C/T]GGCTGTTTGTGTACC | 114088 |
rs58186713 | in-del | -/A | 0.387453 | 0.208822 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010130 | AAGCGAAAAAAAAAA[-/A]GAAAAAGAAAAAGAA | 114088 |
rs58240160 | snp | A/C | 0.420892 | 0.182472 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981380 | CACATATTTCATTTA[A/C]TCTTCAGAAGATTCC | 114088 |
rs58263123 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007048 | TGACTCAGGAGGGCA[A/G]TGAATGGGGGAGGAG | 114088 |
rs58263610 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003177 | CTAGGGACTTTCCTT[C/T]TTATTTTAAATTTGT | 114088 |
rs58348717 | in-del | -/TAA/TAAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064511 | ATCAAAAGTTAAAAG[-/TAA/TAAG]GGGAAGAAAAAGGAA | 114088 |
rs58368926 | in-del | -/CACAGGTGTTTTCA | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025419 | ACACCAACAAGGCCA[-/CACAGGTGTTTTCA]GCGAGACTCAAAACT | 114088 |
rs58417087 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061392 | CATTCCAGCCTGGGT[A/G]ACAAAGCAAGACTCT | 114088 |
rs58530563 | snp | A/G | 0.0244538 | 0.107838 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097006 | ATATCTTGGACCAGC[A/G]AGGTGAGCAGCTGTT | 114088 |
rs58608782 | snp | A/C | 0.468148 | 0.122112 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060456 | TCATTCTTATTTATT[A/C]TCTTATATTCATTCT | 114088 |
rs58735321 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047494 | TAGGACTGATTTGTT[C/T]CCAGAGATATTATAA | 114088 |
rs58885832 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059810 | CTCAAAAAAAAAAAA[-/A]CAAAAAAAACACAAA | 114088 |
rs59165823 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015415 | TTGACACCTTCCCCC[A/G]CCTCCATTTACCTCT | 114088 |
rs59227932 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053609 | AATTTTTTTTTTTTT[-/T]ATTATACTCTAAGTT | 114088 |
rs59344468 | snp | A/G | 0.02016 | 0.0983543 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977944 | CAAGAGTCTTTATCA[A/G]TAGATAATCAGAAGG | 114088 |
rs59517672 | snp | G/T | 0.164873 | 0.23506 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082916 | AGAATACAGAGTCTG[G/T]CTCTTTAAGGGGAAA | 114088 |
rs59851765 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993809 | TGTTAGCACCACAGC[A/G]GACTGTGCTGAGCAT | 114088 |
rs59978383 | snp | A/G | 0.111576 | 0.20818 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049416 | CTTTCAGGCACATCT[A/G]CTACAGGGCTGCCAC | 114088 |
rs60113575 | snp | A/T | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065418 | ATGGATGCTTAAGAG[A/T]GTCCAGGAAGTGCAC | 114088 |
rs60152650 | snp | A/T | | | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982034 | TAGCTACTACAGGTC[A/T]CTGTCAGGTTGTCAT | 114088 |
rs60251657 | in-del | -/ATTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067868 | TCTACTGTTTATTTT[-/ATTTT]GTGTTATGGCTATTT | 114088 |
rs60378597 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085323 | TATTCCCGCACCAAA[G/T]AATAATGTTTAGCAT | 114088 |
rs60407268 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025967 | GCCTCCGACACCAAG[G/T]CTTACTCTCTTTCTT | 114088 |
rs60558660 | snp | C/T | 0.467946 | 0.122472 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060626 | CGCCTGCCACCACGC[C/T]CGGCTAATTTTTTTG | 114088 |
rs60582414 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993988 | CTGAATCCCCAGAAC[C/G]TGTGAATATGTTATT | 114088 |
rs60697917 | in-del | -/A | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059798 | TCAAAAAAAAAAAAA[-/A]CAAAAAAAACACAAA | 114088 |
rs60705836 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067170 | CTCAACATGTTAAAC[C/T]AGTTCCCTCCCCAGT | 114088 |
rs60727032 | snp | C/T | 0.149999 | 0.229128 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071441 | GAAAGTGGAGACAAA[C/T]AGACTTCACTTGAAA | 114088 |
rs60781680 | in-del | -/AAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063484 | AATTATAAATCCAAG[-/AAG]TTCACTGAACTCCAA | 114088 |
rs60882861 | snp | C/T | 0.375996 | 0.215928 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990242 | AGGCTGGTCTCAAAC[C/T]ACTGGCCTCAAGCAG | 114088 |
rs60955870 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092018 | GTTGTGGTTTACCCA[C/T]CCTAATTACCTTGTG | 114088 |
rs61093844 | snp | C/T | 0.238171 | 0.24972 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029803 | TTCACCACTCACATA[C/T]GGAACAGCTGGAACA | 114088 |
rs61319011 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067388 | CTAACTTCTACTGTC[A/G]GTTCTTGCCCTGACA | 114088 |
rs61329273 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067413 | CTGACAGCCAGAGTA[C/T]TCTTTTAAAAATGCA | 114088 |
rs61602291 | in-del | -/AA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007801 | AACACATATTAAACC[-/AA]AAAAAAAAAAAAAAA | 114088 |
rs61755582 | snp | C/T | 0.0482937 | 0.147698 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022864 | CATGCTCCTTGTTGA[C/T]GCGGGCCAGCAGCTG | 114088 |
rs61756358 | snp | C/T | 0.011702 | 0.0755915 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094139 | TAGTTTCCACATGGC[C/T]CCCAGAGCCTTGACT | 114088 |
rs61985021 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50979613 | GAAGCTCCCCCCTTT[C/T]GTGTGGTGAAACCAG | 114088 |
rs61985022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004573 | CAGGGAACACTAATC[A/G]TAAGGGATGCTTTCA | 114088 |
rs61985023 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007819 | AAAAAAAAAAAAAAG[A/G]ACAAAATAAGAGAGA | 114088 |
rs61985024 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024285 | TAAAGAAAGAACTGA[C/T]TGATAAACTCCATTG | 114088 |
rs61985025 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026844 | ACTCCAATGGAAAAG[A/G]TGGGAAGAACAGTAA | 114088 |
rs61985026 | snp | C/G | 0.459347 | 0.136653 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035051 | ATTAAGTGAAAAGAA[C/G]AGATTTCAAGATAGC | 114088 |
rs61985028 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041990 | CAATGTGGCTCACTG[C/T]TGGAGCAGGAAGCTC | 114088 |
rs61985042 | snp | C/T | 0.228253 | 0.249052 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043567 | CCAACTCTGAGGGAC[C/T]AGGGGAGAGTGATGT | 114088 |
rs61985043 | snp | C/T | 0.228253 | 0.249052 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043799 | TTCCAGAATTTCCTT[C/T]CCAAAGGCATAGGGC | 114088 |
rs61985044 | snp | A/G | 0.43221 | 0.171171 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044386 | TACCTGGCTAAAAAT[A/G]ATTTCTGAACCTCCT | 114088 |
rs61985045 | snp | A/G | 0.228253 | 0.249052 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045617 | AAGAGTAAATGTGAG[A/G]TTACTGTCATTATTG | 114088 |
rs61985046 | snp | C/G | 0.224116 | 0.248656 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045912 | AGAAAATCCAGGAAT[C/G]AACTTCAATTCCATC | 114088 |
rs61985047 | snp | G/T | 0.228547 | 0.249078 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046199 | TGGGTGGGCTAGAGA[G/T]AAGTAGGTGTGGTTA | 114088 |
rs61985048 | snp | C/T | 0.227664 | 0.249 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048300 | GCTCTGTTCCTGAGA[C/T]CAGTCCTGACAGTTC | 114088 |
rs61985049 | snp | C/T | 0.121022 | 0.21416 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049302 | TTTTGTTTTACAGAT[C/T]GAAAAGATTATACCA | 114088 |
rs61985050 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050042 | AAACGATGCAGAGCC[A/G]TGAGACAGTTTTTAG | 114088 |
rs61985051 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053746 | ATGCTATCCCTCCCC[C/G]CTCCCCCGACCCCAC | 114088 |
rs61985052 | snp | C/G | 0.479744 | 0.0985793 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054568 | GGAATGAGCCATTGC[C/G]GCCGGCCAATGCTCT | 114088 |
rs61985053 | snp | C/T | 0.386313 | 0.209568 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058211 | CCCTGCATTACAGGA[C/T]GGCACAATCATGGAA | 114088 |
rs61987469 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064453 | ACGGAATAAATAAGT[C/T]CCAACTATAATTATC | 114088 |
rs61987470 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077937 | TTCTGGGCATATAAA[A/G]GCGTTTTGGTTATGC | 114088 |
rs61987472 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086590 | AAGAAGATAGATAAG[A/G]AACAGTCTATGGAAT | 114088 |
rs61987473 | snp | A/C | 0.347032 | 0.230401 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087277 | GATAGCTAAGCAGGC[A/C]GATGGGATTGTGACT | 114088 |
rs61987474 | snp | C/T | 0.490673 | 0.0676508 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089782 | GCTTTGGACTGTACC[C/T]TATGCTCTGAAAAGG | 114088 |
rs61987475 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090164 | AAAAATGTTTACATG[A/G]CACACAGAATGTTCT | 114088 |
rs61987477 | snp | A/G | 0.285519 | 0.247464 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091862 | ACCCAGGCAGCACCA[A/G]TGTCTGTCTACTCAT | 114088 |
rs61987478 | snp | C/T | 0.287867 | 0.247116 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51096054 | CTATTTCTGAGTGCC[C/T]GTAGTTTAGTAAAGC | 114088 |
rs61987479 | snp | A/G | 0.255782 | 0.249933 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096597 | GCCCTTGTAGAAATT[A/G]TCCAATAAACTAGGT | 114088 |
rs66793454 | in-del | -/AAA | 0 | 0 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975014 | AAAAAAAAAAAAAAA[-/AAA]CAGAAGTAAATCCCC | 114088 |
rs66985758 | in-del | -/GAAT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992601 | GATAAATGAATGAAT[-/GAAT]GAATGAATAAATAAA | 114088 |
rs66985763 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992601 | AATGAATGAATGAAT[A/G]AATAAATAAATAAGT | 114088 |
rs67154650 | in-del | -/TTTTT | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988575 | CTGTACAACCATTTC[-/TTTTT]TTTTTTTTTTTTGAG | 114088 |
rs67426903 | snp | A/G | 0.164219 | 0.234823 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011053 | ACCTGGAAGGCCAAG[A/G]TGGAGCTTGGGAGAG | 114088 |
rs71121617 | in-del | -/A | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995774 | CAAAGAAAAAAAAAA[-/A]TCTCTAAAGCAAACC | 114088 |
rs71121618 | in-del | -/TT | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002300 | TGATTTTTTTTTTTT[-/TT]CTTTTTGGTATTTTT | 114088 |
rs71121619 | in-del | -/CAA | 0.0566069 | 0.158427 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006011 | CAACAACAACAACAA[-/CAA]AAACAACGGCAACAA | 114088 |
rs71422010 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996387 | TAAAATAAACTGAGG[C/T]GCTACATCCTCCTGC | 114088 |
rs71422011 | snp | C/G | 0.142947 | 0.22592 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020781 | CCATTCTTTGATAGG[C/G]ATAAATGATGCATTC | 114088 |
rs71422012 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042672 | TTCCCATCCCTTACG[A/T]TGAACATCTTCTTCC | 114088 |
rs71422013 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053631 | CTCTAAGTTTTAAGG[G/T]ACATGTGCACATTGT | 114088 |
rs71422014 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071052 | GGTTTTGGTGGACTG[A/C]TGGGGACGACAAAAT | 114088 |
rs71422015 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072680 | TTTTACTTAGAGACT[A/G]TTTGAATAGCTCTTA | 114088 |
rs71443138 | in-del | -/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984018 | GGAGGAGGGATGGTA[-/G]GAGTGGGTGTGGTCT | 114088 |
rs71443141 | in-del | -/C | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993529 | CCCGCCACCACACCC[-/C]AGCTAATTTTGTATT | 114088 |
rs71443144 | in-del | -/TT | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002289 | ACCACGGCTGGCTGA[-/TT]TTTTTTTTTTTTCTT | 114088 |
rs71443146 | in-del | -/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046167 | CAGGGGTGATGGGGT[-/G]GGGGGTTGAACCAGG | 114088 |
rs71770893 | in-del | -/AA | 0.102726 | 0.202016 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041805 | GCCTAATATGATGTT[-/AA]GTGTTTCAAATAATG | 114088 |
rs72053355 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013227 | AAGTGTCTAACTTCA[-/T]TTTTTTTTTTTTTTT | 114088 |
rs72353788 | in-del | -/CAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006012 | ATCAACAACAACAAC[-/CAA]AAAAACAACGGCAAC | 114088 |
rs72685397 | snp | A/G/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978515 | CCCTCTGTCTGGAAG[A/G/T]CTCCACGCAACTCAC | 114088 |
rs72685401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982186 | CTGGGCGGGTGAGGA[A/G]CGTTGTGTAGCGTTT | 114088 |
rs72687113 | snp | C/T | 0.0228947 | 0.104514 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996640 | AGCAAGGGCCTTCTG[C/T]GTTGCATCTAGGAAA | 114088 |
rs72687116 | snp | C/T | 0.040671 | 0.13668 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999237 | AAGAATTGGGAAAAC[C/T]GGGAGAGTTACTTTC | 114088 |
rs72687121 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011012 | TCAATTGTTCTGCAT[A/C]TTTTTCCTTGCGTGG | 114088 |
rs72687142 | snp | A/G | 0.228253 | 0.249052 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045390 | TTCATTTTAACGTAA[A/G]ATAGAACTTTCACCT | 114088 |
rs72687143 | snp | C/T | 0.228253 | 0.249052 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045400 | CGTAAGATAGAACTT[C/T]CACCTTTTAGAGCTA | 114088 |
rs72687148 | snp | C/G | 0.227959 | 0.249026 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049579 | ATGCCTGTAATCCCA[C/G]CACTTTGGGAGGCCG | 114088 |
rs72687152 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060106 | CTTCAGAATTTATAA[C/T]GGGCTTTCTAGCTTT | 114088 |
rs72687155 | snp | A/T | 0.240765 | 0.249829 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062840 | GCAGAGATATCTGCA[A/T]CTGCCAAGTGAAGAG | 114088 |
rs72687158 | snp | C/G | 0.251014 | 0.249998 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068280 | CTGGCCCCCAGTAAG[C/G]TCACACTCAAAGCAG | 114088 |
rs72687159 | snp | A/C | 0.251014 | 0.249998 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068473 | ATGACATTTATTAAG[A/C]GCTGCCTGTGTGCCT | 114088 |
rs72687160 | snp | A/T | 0.251014 | 0.249998 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068549 | CCACAACCTTGTAGA[A/T]GTTATTTTTATCCCC | 114088 |
rs72687161 | snp | A/T | 0.251014 | 0.249998 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068711 | TGAGAAGAATAAGGA[A/T]GTAAAGTTATGTAGA | 114088 |
rs72687162 | snp | A/G | 0.251296 | 0.249997 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068720 | TAAGGATGTAAAGTT[A/G]TGTAGAATTAGAAGA | 114088 |
rs72687170 | snp | C/G | 0.398575 | 0.203114 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083917 | AGCTATATGATTCTA[C/G]GCCATCACTCAACCC | 114088 |
rs72687173 | snp | A/G | 0.399073 | 0.200692 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086076 | GAGAAAAATGACTCA[A/G]TTTCTCAGTAATTTT | 114088 |
rs72687174 | snp | C/T | 0.490007 | 0.0699769 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086224 | AGTTAAACATGTGAG[C/T]TGTAGAGTCAGACAG | 114088 |
rs72687175 | snp | C/T | 0.397633 | 0.201754 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086273 | CCCTGCCAATTACAA[C/T]GGGTGTGACTTCATA | 114088 |
rs72687177 | snp | G/T | 0.346147 | 0.230772 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087195 | GTCTAAGAAACTGGG[G/T]GAGGGCAAGCGTAGT | 114088 |
rs73288810 | snp | A/G | 0.142947 | 0.22592 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974810 | ATCAAGACCATCCTG[A/G]CCAACATGGTGAAAC | 114088 |
rs73288814 | snp | C/T | 0.145642 | 0.227177 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978843 | TCTATAGATATTTGC[C/T]GAATGAATAAATGAG | 114088 |
rs73288820 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983488 | AAAATTACTTGTATA[C/T]GCTTAAAAAGCACCA | 114088 |
rs73288824 | snp | C/G | 0.147991 | 0.228242 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986597 | TTTACAAACTGTTTC[C/G]TATTCCATATTTTCC | 114088 |
rs73288853 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012054 | TTTTTTTGTTCTTAA[C/T]GTGTTATTGTGGCAA | 114088 |
rs73288860 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017803 | GCATTGCCAAAGTGA[C/G]TGGGGGGGCTGTTCA | 114088 |
rs73288862 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020426 | AGCTTTGCTGCTATG[A/G]GGGACAGCCAGCCAC | 114088 |
rs73288863 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024536 | TCAAAACATAAGAAT[C/G]CTAAACAGTACAGAA | 114088 |
rs73288867 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025773 | GGTAGGGCAGAAAGA[A/G]TAGAGTAAAGAACAG | 114088 |
rs73288875 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028818 | ATGCTGAGAATCACC[A/G]AGGTCTCCCAGAAAG | 114088 |
rs73288876 | snp | A/G | 0.151001 | 0.229563 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028856 | GTTGTTCAAGCCTGA[A/G]GGAGAGAAACAAAGA | 114088 |
rs73288879 | snp | C/T | 0.112631 | 0.208878 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035875 | GTAACTGCCTAACAA[C/T]GCACATAAAATGGTT | 114088 |
rs73288887 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041281 | ATGACAAAATAACTG[C/T]GCAATCATTTCCAAA | 114088 |
rs73288888 | snp | C/G | 0.125528 | 0.21681 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041807 | CTAATATGATGTTAA[C/G]TGTTTCAAATAATGT | 114088 |
rs73288892 | snp | G/T | 0.0611083 | 0.163768 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045782 | GTCCATTATTTGTAA[G/T]AAATAATTTTTTTCA | 114088 |
rs73288894 | snp | C/T | 0.111576 | 0.20818 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047924 | AAGTTCGCACCACTG[C/T]ACTCCAACCTGGGCG | 114088 |
rs73288895 | snp | C/T | 0.112983 | 0.209108 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048510 | AGTGAAAGTCATTGG[C/T]TAATTACTAGTGACA | 114088 |
rs73288897 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052320 | ATAACAAAAGAGTCA[A/G]GGTCGGCGAATATAA | 114088 |
rs73288898 | snp | A/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053561 | TTTATTTATTTATTT[A/T]TTTTTACTTTTTAAT | 114088 |
rs73288900 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056845 | TTGCTGGAACCTTTC[C/T]CTTATCTTCCCTCAA | 114088 |
rs73290818 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083723 | GAGTTGAGATACATA[C/T]CCAAGTGGAGATGCC | 114088 |
rs73290819 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085843 | AGAGACAATGCTCCA[C/T]GGTTGAGCTGGTAAA | 114088 |
rs73290824 | snp | C/T | 0.0670745 | 0.170406 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097100 | AAAGTTTATGCTTAG[C/T]TCAAAGTAAAGAAGA | 114088 |
rs74052111 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980382 | ATTTTTTTGAGATCT[A/G]GCAATATTGAACTTC | 114088 |
rs74052112 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982156 | ACCCAACAAGCTCAG[C/G]ACCATAACATACTCC | 114088 |
rs74052135 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983569 | TATATTATTTAGTTT[G/T]TTGGGTAAAAAACTG | 114088 |
rs74052146 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001130 | CTTGAACATTGAAGA[C/T]ATTATCCCTAAAGGA | 114088 |
rs74052519 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013782 | ATTTTTTATTCATAA[A/G]ATAACAGGAAGGTTA | 114088 |
rs74052520 | snp | A/C | 0.0633504 | 0.166319 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014173 | TACTGAAATAAATAC[A/C]TTACTCAGTCCTCAT | 114088 |
rs74052588 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032839 | ATTCAATAAGTAGTA[C/T]AGGTTGAATATCCCT | 114088 |
rs74052594 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043061 | ATACATGATATAGTG[C/T]TTCTTCCTCTGAATT | 114088 |
rs74052596 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044820 | AGATGGGCTAGATAA[A/G]TAACTGCCACTCCCA | 114088 |
rs74054003 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052514 | ATTTATGTTTAATCC[C/T]TATGGATTTGATGTG | 114088 |
rs74054004 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052875 | GAAAATTTGCCATTA[G/T]GCCAAGCATGGTGGC | 114088 |
rs74054009 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056042 | TGTCCAAAAACTAAC[C/T]TCACTACTCAATACT | 114088 |
rs74054012 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056170 | ATCTTTGATAAGAAA[C/T]TACAATAAGAAATTC | 114088 |
rs74054017 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063253 | TATACTGGAGTAGGC[A/G]GAATAAAAAATTCGG | 114088 |
rs74054019 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063272 | TAAAAAATTCGGAAG[A/G]CATCAATAATAATTA | 114088 |
rs74054021 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063355 | GCCTGCAAGAAATAA[C/T]TAATCAGCCTAATAT | 114088 |
rs74054023 | snp | G/T | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063461 | AAATGCTCCCAAATT[G/T]GGTTAAAAAATTATA | 114088 |
rs74054024 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063673 | AAAAAAGGAAAGATG[A/G]TAATGGAATCAAATT | 114088 |
rs74054025 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063791 | TAGATAAATAGAAGC[C/T]AAGACAATTTGTTTC | 114088 |
rs74054026 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063818 | TTTCCAGGAGATTTA[C/T]ACTACAGGAAATGTT | 114088 |
rs74054028 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064924 | TATAAATCATAAATA[A/G]AGCTTAAGGCACAGA | 114088 |
rs74054031 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066337 | CTCATTCATCTCCAT[C/T]TTTGCAAACCCAAAG | 114088 |
rs74054032 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066488 | GTGTCACTGGCTGTC[A/G]CTTCTCAGTGTCTTT | 114088 |
rs74054034 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068292 | AAGGTCACACTCAAA[C/G]CAGAAAAATAAATAG | 114088 |
rs74054039 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078205 | TTTAACATGGTTGGG[A/G]AGATAAAAGAACAGT | 114088 |
rs74054040 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079145 | ATCCAAAAGCCTTCA[C/T]AATATGCAAATTAAA | 114088 |
rs74054041 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079149 | AAAAGCCTTCATAAT[A/G]TGCAAATTAAATAAT | 114088 |
rs74054042 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080112 | TGTTTTCTGTGTGAG[A/G]GGCATAGCAAAACTA | 114088 |
rs74054044 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081700 | GCAACCTTGGATCAT[C/G]CCCTTCTCACGTTTG | 114088 |
rs74054046 | snp | A/C/T | 0.0441095 | 0.141807 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081948 | GAGTTTTTATAGAAC[A/C/T]CAATCTCCAGCCACC | 114088 |
rs74054049 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083998 | ATAATGAATGGCAAG[C/T]AAACAAGAATTGAGG | 114088 |
rs74054052 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087765 | CAGAGCAATATTAAA[C/G]TTTTAAGCTTTTCAT | 114088 |
rs74054053 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091553 | AAAACATAAACTATA[C/T]GAGAAAACTGGCTGC | 114088 |
rs74055306 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006939 | CAGAGAGCATGAACT[C/T]GCAGTTCCCATACCC | 114088 |
rs74055308 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011036 | TGCGTGGATGGTGGG[G/T]GACCTGGAAGGCCAA | 114088 |
rs74244447 | snp | G/T | 0.170408 | 0.236992 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078677 | TGATATTTTAAAGTA[G/T]TACTTACGTGGAATC | 114088 |
rs74332766 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037407 | TTATCCTGCATGCAT[A/G]ACCTAGACCCCTGAT | 114088 |
rs74336842 | in-del | -/A | 0.447297 | 0.153538 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045058 | CATGTGAAAATATGG[-/A]AAAAAAAATCAAATA | 114088 |
rs74381050 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083395 | CAGTAGCTCGGACTA[C/T]AGGCATGCGCCACCA | 114088 |
rs74418461 | snp | G/T | 0.040671 | 0.13668 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090551 | GAAAATCTTTGCTCA[G/T]TAGCATGAACACAGA | 114088 |
rs74421221 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023555 | AGATATGACCCAACA[C/G]CTTGCAGGGGAAAGG | 114088 |
rs74463491 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021441 | ATGACATTGGGCACC[A/T]CTCTCCTGGAAGCCC | 114088 |
rs74477509 | snp | A/C | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072669 | ACTTTTTTTTTTTTT[A/C]CTTAGAGACTATTTG | 114088 |
rs74484323 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045066 | ATATGGAAAAAAAAA[-/A]TCAAATACTGCATAG | 114088 |
rs74496283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084073 | GTATTTAAAAATATA[C/T]GGGAAATATTTATGT | 114088 |
rs74598030 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061815 | TAAGCTTTTTGGATC[C/T]GTGAGTTGAAGTAAC | 114088 |
rs74710659 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076794 | GAGGTCAAATAACTA[A/G]CCCAAGTTCACAGCC | 114088 |
rs74731031 | snp | C/T | 0.17332 | 0.23795 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080877 | AAGAAATGATTTCCT[C/T]CTGCTTTTGGACTTT | 114088 |
rs74784420 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038063 | CCATGCCCGAATCCC[C/G]AGAACCGGTGATTTT | 114088 |
rs74802818 | snp | G/T | 0.0663309 | 0.169604 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018581 | AGATAATGGTGAAAA[G/T]AATGATAATTATTCT | 114088 |
rs74845706 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039384 | CAAGCTGGAAACAGC[C/T]CAGATGTCTACCAAC | 114088 |
rs74846861 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014258 | CTGAAGGAGCTATCT[C/G]AGTGCTGGGGCTCTC | 114088 |
rs74854568 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023276 | GAGGGCCACATATGT[C/T]CAGCTATGTATGGTG | 114088 |
rs74878259 | snp | A/G | 0.0166909 | 0.0898156 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977274 | GAACAGGCAGCTGGC[A/G]CCTCCACGGCACATC | 114088 |
rs74932403 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075244 | CCCTATTTAGCCACT[A/G]CTATTCTAGGTTCCT | 114088 |
rs74966412 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032189 | ATCAGATAGTAGGAA[C/T]TGGGCCAGACAGAGC | 114088 |
rs75117095 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995519 | TGATCTCCCCTGCAT[A/G]ACGTTACCTTTAGAT | 114088 |
rs75132764 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064439 | GTAAAGACTAGCAGA[C/T]GGAATAAATAAGTCC | 114088 |
rs75144305 | snp | A/C | 0.0861826 | 0.188849 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029866 | TTGCTCCAGCCTCCC[A/C]AAAAAAGAGAATTCT | 114088 |
rs75164702 | snp | A/G | 0.377385 | 0.215112 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987760 | AAGGCATTTACAACT[A/G]TATTTATGTCAATAA | 114088 |
rs75179605 | in-del | -/TTTTTTTTTG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027153 | TTTTTTTTTTTTTTT[-/TTTTTTTTTG]AGACAGAGTCTCACT | 114088 |
rs75254705 | snp | A/T | 0.0607341 | 0.163335 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009977 | GTCAAGAAGGTAGAC[A/T]TCTTACAAACTTAGA | 114088 |
rs75274687 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063267 | CGGAATAAAAAATTC[A/G]GAAGGCATCAATAAT | 114088 |
rs75281258 | snp | C/T | 0.127599 | 0.217986 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060072 | GGAGTCACAGATAAA[C/T]CACCTCCTGACTGGA | 114088 |
rs75305516 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988789 | CATGCCCTTCCCCAT[A/G]GGCATGTAGTGCACA | 114088 |
rs75308739 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019674 | AGTCATTCTCTCTCA[A/G]TCACAACAATAACAG | 114088 |
rs75315861 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086365 | AATGCTGTAAAAATC[-/T]TTAGAGCAGTGCCTG | 114088 |
rs75362989 | in-del | -/A | 0.103082 | 0.202275 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047650 | TAAGGCAACATACCC[-/A]AGGGAGGTATGGTCT | 114088 |
rs75384799 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991838 | GGACATATCCAAGTT[A/G]CACCACAGCTGTGGA | 114088 |
rs75390983 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064404 | ATTAAATTCAAAAGT[C/G]TAACTACTCCAATTA | 114088 |
rs75411239 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058918 | AAGCAAGAATTCTCA[G/T]GTAATGTTTTGCATT | 114088 |
rs75422786 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043601 | AGAAGTTTATATGAA[A/G]TTTGGATGGGAAACT | 114088 |
rs75500586 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002452 | AACCATGTTTTTGCC[A/C/T]GCTGCTTAAAAATTT | 114088 |
rs75501780 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083744 | TGGAGATGCCAGCGA[C/G]CTTTAGGGTTCAATG | 114088 |
rs75546703 | snp | G/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002139 | TGTTTTTCTTTTTTT[G/T]GAGACGCAGTCTCGC | 114088 |
rs75563387 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047942 | TCCAACCTGGGCGAT[A/G]CTGTGAGACCCTGTC | 114088 |
rs75662647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006519 | CGCAAGCATCTGACA[A/G]ATGAAAATTATTCAG | 114088 |
rs75680591 | snp | G/T | 0.17461 | 0.238362 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086916 | GACACTCAAAAAAAG[G/T]TTTCTTGCTTTTGCA | 114088 |
rs75704983 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027303 | CGTGCACCACCACAC[C/T]GAGTGAACTTTTGTA | 114088 |
rs75724366 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999756 | CCCAGAACGGCTGCT[C/T]CCTTAGGAAGCTCCA | 114088 |
rs75737552 | in-del | -/ATCTGTTTCAGACAATCAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086784 | GACTGAAATGACCAG[-/ATCTGTTTCAGACAATCAG]GTACAAGCAGGAATT | 114088 |
rs75751509 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997133 | TTGATTAAAATGACA[C/T]CCCAAAGTGTCAGAA | 114088 |
rs75791984 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023274 | TTGAGGGCCACATAT[G/T]TTCAGCTATGTATGG | 114088 |
rs75828197 | snp | G/T | 0.0941369 | 0.195465 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034147 | TGAATTTTCCGAATT[G/T]TTTTCCAGTTTTTGG | 114088 |
rs75855232 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052272 | TGTAAAGCAAACTAC[C/T]AACTCCCTATCACTT | 114088 |
rs75859882 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010564 | AAGCAAACTGGACCA[C/T]TGGAAAGCTTCTTCA | 114088 |
rs75903501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985099 | ATCCATGATTACAAT[A/G]TAGTCCTGAAGAGAT | 114088 |
rs75910585 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999373 | CACACACAACACACA[C/G]ACACACACTCTCACA | 114088 |
rs75924013 | snp | A/G | 0.040671 | 0.13668 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086137 | TTGTTATGTCATTGA[A/G]GTTTGTAAGTTCATA | 114088 |
rs75962801 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079423 | TACTAAGTATTTGTC[C/T]TATTTCATTTCCATG | 114088 |
rs75962961 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059036 | GAACAGGCCTGTAAA[A/G]GAAGAGCTAATGAAA | 114088 |
rs75978054 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005390 | CTATGTGCTAAAAAG[C/G]CTTGGTGAACTGTTA | 114088 |
rs75978552 | snp | C/T | 0.119978 | 0.213528 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036866 | AATTTGGGCTATCTA[C/T]ATCTATTGTGTTAAC | 114088 |
rs76013289 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998492 | TGGTAGTTATTAGCA[C/G]CTAGGGCTTAAAAAA | 114088 |
rs76023433 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079510 | GTTTCAAAAGAAAAG[-/A]TATTATGTGAGTGCA | 114088 |
rs76058763 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087519 | AGGGTTGTGAGAACA[A/C]CCCAGGGGAATGATC | 114088 |
rs76064637 | in-del | -/AA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064678 | GAGGATATCACACAC[-/AA]AAAAAATCCTATAGA | 114088 |
rs76120110 | snp | A/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054448 | CAGCTGTTTTTTGTA[A/T]TTTTTTTGTTAGAGA | 114088 |
rs76122204 | snp | A/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072668 | TACTTTTTTTTTTTT[A/T]ACTTAGAGACTATTT | 114088 |
rs76152035 | snp | A/G | 0.1652 | 0.235179 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070550 | TTTTGGAATATTTGC[A/G]TTATAATGGTTCAGC | 114088 |
rs76160186 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043836 | CCTGTTTGGTTTAAC[A/T]TTTTTATTTTAATGC | 114088 |
rs76162422 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088989 | CAAGCTAAAGCAAAG[-/A]AAAAAAAAAAAAGAC | 114088 |
rs76220673 | snp | A/C | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006025 | ATCAACAACAACAAC[A/C]AAAACAACGGCAACA | 114088 |
rs76232137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033881 | GAATGTATTCCAAAG[A/G]TTTATATTATGCATA | 114088 |
rs76236223 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976898 | AAGCTTAAGAAAAAA[A/G]GTTAGCAGGAGAATT | 114088 |
rs76276077 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066906 | ATACTCTTAAATTAG[G/T]CTTTCAGTTAGTTTA | 114088 |
rs76284519 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013424 | CCACTATTTTGATTA[C/T]TGTCGCTTTATAATA | 114088 |
rs76368573 | snp | A/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072994 | TAATGTTTTATTTAT[A/T]TTTTTTTTGGCAACT | 114088 |
rs76379481 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062127 | ATGATATTGTGCTTT[-/T]TCATTTCTAGTATTT | 114088 |
rs76441183 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988590 | TTTTTTTTTTTTTTT[G/T]TGAGTTTTTTCCCCA | 114088 |
rs76456321 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093752 | CTCGAGCGTGCCTAG[A/C]GGCCCTGGGCACTGG | 114088 |
rs76466543 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013330 | ACCTTGTGAAAAATC[A/C]TTTGAGCAAGTATGT | 114088 |
rs76480595 | snp | G/T | 0.177503 | 0.239258 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064726 | ATATTATTAATAGCT[G/T]TATTACAATGAAATC | 114088 |
rs76481199 | snp | C/T | 0.111576 | 0.20818 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048706 | TCCCATCTCGGGGGC[C/T]GGGCGCAGTGGCTCA | 114088 |
rs76522263 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994980 | TCAGAGAACTATCCA[A/C]ACTTGGACTCATATA | 114088 |
rs76525318 | snp | A/G | 0.14933 | 0.228835 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059466 | AAGCATTGGGAGCAC[A/G]ATGAAGAGAATGAAA | 114088 |
rs76529768 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998493 | GGTAGTTATTAGCAG[C/T]TAGGGCTTAAAAAAA | 114088 |
rs76539374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086322 | TTTCTCACAGGAAGA[C/T]GTGTGGATTATGAAG | 114088 |
rs76566913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019205 | GACAAGAAACCTGGA[A/G]GTCCAGTGTGCTCTG | 114088 |
rs76630944 | snp | G/T | 0 | 0 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978766 | TTTATCTGTTTTTTT[G/T]TTTTTTTTTTTCACT | 114088 |
rs76645387 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035046 | AACACATTAAGTGAA[A/C]AGAACAGATTTCAAG | 114088 |
rs76655218 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073500 | TATGCAACAATATAA[A/G]TGGATCCAAAAAACA | 114088 |
rs76764255 | snp | A/T | 0.149665 | 0.228982 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062358 | TCTCGATTTTTTTGT[A/T]TGTCTCACAACTTTT | 114088 |
rs76863053 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059765 | ATCGTGCCACTGCAC[C/T]CCAGCCTGGGTGAAA | 114088 |
rs76964479 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976124 | TCACTCTTTTTTTTT[C/T]CAACTGTCAATTTTT | 114088 |
rs76987504 | snp | A/C | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074255 | AAGACTCCGTCTCTA[A/C]AAAAAAAAAGTAATG | 114088 |
rs77090346 | snp | A/G | 0.212122 | 0.247114 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071970 | CCCGGACTCAGCAGC[A/G]TGAGGGAGCAGCATG | 114088 |
rs77115927 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068171 | TCTGCAGACCACATC[C/T]TGAGAACCACTGAAC | 114088 |
rs77152692 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011454 | ATCTCAGTCTCCAAG[C/T]AGCTGGGACTACACT | 114088 |
rs77174108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033542 | TCAGAACAATTTGCT[C/G]TGGTCCCATTTTGTC | 114088 |
rs77208684 | snp | C/T | 0.079617 | 0.182947 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039077 | CTGAATTTAGAAGGC[C/T]TTACCAGGCCTTTAC | 114088 |
rs77262729 | snp | C/T | 0.388775 | 0.207946 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070975 | CAGAGATTCAGAGAC[C/T]GGGGACTACCATATA | 114088 |
rs77287443 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047133 | AGCTGGGGTTGACAC[C/T]TGTGTTTACCATGAA | 114088 |
rs77319178 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990789 | GGCAAGACATGTCAC[A/G]AAGAATTGTACAGTG | 114088 |
rs77367267 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029777 | CCGAGAGGATACCCC[C/T]GAGTGAAGGTTTCAC | 114088 |
rs77375119 | snp | A/C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028835 | GGTCTCCCAGAAAGA[A/C/T]GACAAGTTGTTCAAG | 114088 |
rs77407560 | snp | C/T | 0.215446 | 0.2476 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078133 | GCCTCACTCAGCCTA[C/T]GTCAGGCCTTGAGGT | 114088 |
rs77425813 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008223 | ATGCAGTGGTGATTA[C/T]AGGAATCTGTACATA | 114088 |
rs77444613 | in-del | -/AAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063483 | AAATTATAAATCCAA[-/AAG]GTTCACTGAACTCCA | 114088 |
rs77453726 | snp | A/C | 0.163236 | 0.234461 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073789 | ATTTCTTCACTAAAA[A/C]TTTCTGTAACATATC | 114088 |
rs77458384 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078642 | ATGATATTTACTGTA[C/T]AACATACAACGATAT | 114088 |
rs77490431 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013242 | TTTTTTTTTTTTTTT[G/T]GCATGTGGATATCCA | 114088 |
rs77514686 | snp | A/G | 0.157311 | 0.232183 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067223 | GCCATTATTTAGCCC[A/G]TTTCTGAGGCCCCCT | 114088 |
rs77521448 | snp | A/C | 0.170808 | 0.23734 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097156 | ATGCAGTGTTGGGTT[A/C]GCAAAAAGAACAACA | 114088 |
rs77532845 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093450 | TCAGGTCCCAACTCC[C/G]GAAGGGTTCAGGCCC | 114088 |
rs77533096 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000960 | GAATGGGGTGCACAG[A/G]GGAACTGAACAGGAT | 114088 |
rs77544274 | snp | C/T | 0.105924 | 0.204309 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036581 | TAATACCTAATACAA[C/T]GTAAGTACTATGTAA | 114088 |
rs77551045 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052503 | AGCGTCATTTAATTT[A/G]TGTTTAATCCCTATG | 114088 |
rs77557045 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032685 | GAGTCTGTGTCCAGG[A/G]AACCCAGTCTAAAAT | 114088 |
rs77614974 | snp | C/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070187 | CTAAGCACAAGAAGG[C/G]TGCAATGCTTGGGGA | 114088 |
rs77644109 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049514 | CATTCAACAAATATA[A/G]TGTATGTGTAAGTGT | 114088 |
rs77674758 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059659 | AAAAATTAGCCGGGC[A/G/T]TGGTGGCACACACCT | 114088 |
rs77712910 | snp | A/G | 0.040671 | 0.13668 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091604 | TAAGTAAATAAGGTG[A/G]GGGAGTAATGTTTGT | 114088 |
rs77731895 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982782 | GACATTAGGTGCAGA[C/T]AGAATGATGTCTTTG | 114088 |
rs77804697 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031910 | ATACTAAACAAATCT[C/T]ACCATTTGTATTGTG | 114088 |
rs77814099 | snp | A/T | 0 | 0 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096263 | AGGGAGGGAGGGAAG[A/T]AGGGAAAGAGGGAGA | 114088 |
rs77832461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043644 | TCATGACCTAGAGAA[A/C]TTTTATCCCTTTCTA | 114088 |
rs77868942 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080790 | TACTGAGGTAGACTC[C/T]GTTTCCAAAGCCAGA | 114088 |
rs77885707 | snp | A/T | 0.0486741 | 0.148216 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978934 | TTTCTACCCCTTAGG[A/T]CCTAACAGAGCCAAA | 114088 |
rs77961518 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052047 | GGGGAGGGAAAAGAA[A/G]AGAAGAGAAGAGAAG | 114088 |
rs77981910 | snp | G/T | 0.164873 | 0.23506 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079989 | GCAAGTAGTGCAAAT[G/T]AATGGGGAGAGGAGC | 114088 |
rs77999310 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096543 | GATAATTTAAAAGTA[C/G]TTTATTGTCCAGAAA | 114088 |
rs78002526 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087598 | AACCTAGATGGTCTC[G/T]GATAGTGTAGGTACA | 114088 |
rs78123550 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096476 | AGTTCTAGAAATATT[C/T]CAATTTTCCACCTTC | 114088 |
rs78142823 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052215 | CAATATATATTTTTC[C/T]AAAATCATTAATATG | 114088 |
rs78156576 | snp | C/T | 0.180383 | 0.240111 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042963 | ACATGTCTCTATATA[C/T]CTATTCCTGGCATAA | 114088 |
rs78205147 | snp | A/T | 0.119978 | 0.213528 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040875 | TTCTGAAAATAAAAT[A/T]CAACCTTATTCTAAT | 114088 |
rs78210005 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044392 | GCTAAAAATAATTTC[C/T]GAACCTCCTCTGCAG | 114088 |
rs78242576 | snp | G/T | 0.0887219 | 0.191022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002125 | TGTGTGTGTGTGTGT[G/T]TTTTTCTTTTTTTTG | 114088 |
rs78261949 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993940 | CATAAAGTATAGTAC[A/T]AAGAATAATGGGCCA | 114088 |
rs78292254 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992959 | CTCTTTTCTCTAATT[A/G]TCACTGACTACCTTC | 114088 |
rs78299949 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087868 | TCAATTAGACCAGTC[A/T]TTTGGTATCATGTAT | 114088 |
rs78316550 | snp | C/G | 0.0411084 | 0.13764 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049373 | AGTTAGGGTCTGTGC[C/G]TGCAGTGGAGTCTTG | 114088 |
rs78326232 | snp | C/T | 0.106278 | 0.204558 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035612 | TCAGACAAAGGAGAA[C/T]GCTATACCACCCGGA | 114088 |
rs78381314 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023275 | TGAGGGCCACATATG[G/T]TCAGCTATGTATGGT | 114088 |
rs78397140 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009987 | TAGACATCTTACAAA[C/T]TTAGACACTTAGACA | 114088 |
rs78447636 | snp | A/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015536 | TTTTTTTTTTTTTAG[A/T]TAGGGTCTCCCTCTG | 114088 |
rs78448733 | in-del | -/AGGAAGGA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066083 | GGAAGGAAGGAAGGA[-/AGGAAGGA]GGGAGGGAGGGACGG | 114088 |
rs78492824 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050671 | ATATGATCCTATGTG[C/T]CTTCTGAAGCCAGGT | 114088 |
rs78493088 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984505 | ATGTTTTGTTTCTAT[A/C]AATTATCACTTCAAT | 114088 |
rs78512275 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031233 | TAGCCAGGGTCCTCT[A/G]AGCCCTCTTCTTACC | 114088 |
rs78551501 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975573 | AAATTAGGTACACTT[A/C]ACTAGAAAAAGATTG | 114088 |
rs78610747 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992839 | ATTGTCTAGGCCCAC[A/T]TTTTAGAAAGCAGTT | 114088 |
rs78659417 | snp | A/G | 0.111576 | 0.20818 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051232 | TCCTGAAAATTTCCT[A/G]TATCTTTTGTCTTTG | 114088 |
rs78793252 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067204 | CTTCATCTTAATACA[C/T]AGTGCCATTATTTAG | 114088 |
rs78793372 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059763 | AGATCGTGCCACTGC[A/T]CTCCAGCCTGGGTGA | 114088 |
rs78904768 | snp | A/G | 0.127254 | 0.217792 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050031 | ATTTTGGAAGTAAAC[A/G]ATGCAGAGCCGTGAG | 114088 |
rs78915552 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096688 | AAGTCCCCATTGTTA[C/T]TTAAAGCCATGTTAA | 114088 |
rs78975770 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081308 | AGACTTCACCTCACA[C/T]CCACTAGAAAGACTA | 114088 |
rs78976413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017512 | GAATACTGTATCCTC[A/G]TACAGAGAAGTTAAT | 114088 |
rs79016401 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037297 | AAATATGATTGTGTA[A/G]GTTAGCTAGGAAACC | 114088 |
rs79020585 | snp | C/T | 0.162253 | 0.234095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074625 | TTGATCCTTCCACCC[C/T]ACCCTGCCCTTTTCT | 114088 |
rs79059968 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086895 | ATGTTTATTTATTCA[G/T]GACTAGACACTCAAA | 114088 |
rs79093121 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013243 | TTTTTTTTTTTTTTT[G/T]CATGTGGATATCCAA | 114088 |
rs79110879 | snp | A/T | 0.0803491 | 0.183626 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066725 | GCATTTATGGACAGA[A/T]AATGGAAATGAGGTG | 114088 |
rs79111312 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985154 | TTTAACATTCTATTT[G/T]CTAGGCAGTGTTCGC | 114088 |
rs79150092 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092521 | CTGAGCAAGGCCACA[G/T]CTGAGGCCTGGACAC | 114088 |
rs79154090 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097671 | TCCTTTTTTTTTTTT[G/T]AGACTGGAGTCTTGC | 114088 |
rs79169925 | snp | A/T | 0.176861 | 0.239062 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063742 | CATCCAAAGAAAATA[A/T]CCTTCAAAAATTAAC | 114088 |
rs79190060 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052060 | AAGAGAAGAGAAGAG[A/G]AGAGGAGAAGAGAAG | 114088 |
rs79199177 | snp | A/C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023273 | TTTGAGGGCCACATA[A/C/T]GTTCAGCTATGTATG | 114088 |
rs79257379 | snp | A/G | 0.101301 | 0.200969 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035730 | TGGTTAGGGCTCTTC[A/G]AAAAGAAAGGGTAGC | 114088 |
rs79302548 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059764 | GATCGTGCCACTGCA[C/G]TCCAGCCTGGGTGAA | 114088 |
rs79440789 | snp | A/G | 0.138546 | 0.223781 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053172 | TTCAAAAAAAAAAAA[A/G]AGAGAAGAAAACTTG | 114088 |
rs79502931 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045151 | AAGCCACCAGCTGCT[C/G]AGCTGGTGAGCTGGC | 114088 |
rs79570917 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076755 | ATTATCTCCATTTTC[C/T]AGATGAGAAAACTAA | 114088 |
rs79601690 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090110 | CTGGGTACAAAGAGG[A/G]ATAACTGTCTTCTCT | 114088 |
rs79605425 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076553 | GGTTTATTACAAAAG[C/G]CTTTCTCATACATTC | 114088 |
rs79639220 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010232 | GGAGTTTATTTAGCC[A/G]GCACTTACTTCCATG | 114088 |
rs79661714 | snp | C/T | 0.338976 | 0.23363 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070839 | GACCAAATATGCACA[C/T]CTTGCTTGTATCATC | 114088 |
rs79808525 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076769 | CCAGATGAGAAAACT[A/G]AAGCACAGAGAGGTC | 114088 |
rs79885236 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085488 | AAACGATATCCTCCT[C/T]GGTTCACATATTCCT | 114088 |
rs79894156 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034908 | GAATAATAATAGTAC[C/T]CATCTTGCTGGGTTG | 114088 |
rs79911335 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998491 | ATGGTAGTTATTAGC[A/T]GCTAGGGCTTAAAAA | 114088 |
rs80006885 | snp | C/T | 0.102726 | 0.202016 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040297 | TATTTGATGCTGGTG[C/T]CCCTCACTCAGAGGC | 114088 |
rs80016229 | snp | C/T | 0.104149 | 0.203046 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989027 | AGCTCCACTCTCCAA[C/T]TGTAGCGTTACTATC | 114088 |
rs80054202 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029493 | TGATCATTGATGCAA[C/T]GGGACTTTGAGGGAA | 114088 |
rs80063331 | snp | G/T | 0.170408 | 0.236992 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079751 | ACACACCAGGTGGAC[G/T]AGGTAGAGAGACTTC | 114088 |
rs80077959 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093981 | CTGCAATGCACCAGA[C/T]CAGGGAGGTAAACAT | 114088 |
rs80082801 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007882 | ACATACCAAGTACAG[A/G]AACGCATTTAACTGC | 114088 |
rs80087134 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035295 | TAAAGAATAAAAAGT[A/C]ATTTCTTAAATAAAA | 114088 |
rs80091146 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048449 | ACAGTTAAGAAAGTT[A/C]ATGTGTTTGTCTGCC | 114088 |
rs80213951 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023407 | GGTCTTCAATATTAA[C/T]AATAATCCAATGAGA | 114088 |
rs80216943 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075763 | TCCCAAGGCGGGGAG[C/T]GGGTCTGATCGATCT | 114088 |
rs80225303 | snp | G/T | 0.021333 | 0.101051 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995130 | TATCTGGGATTACAG[G/T]CATGAGCTACGGCAC | 114088 |
rs80268329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069482 | TAGAACAAAGAATTG[A/C]CCATCCCCAAATGTC | 114088 |
rs80277731 | snp | C/T | 0.00993419 | 0.0697739 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977210 | GCCAACTCTGCACCC[C/T]ACCACGGCTGGCTGA | 114088 |
rs80292596 | snp | A/G | 0.195214 | 0.243923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028956 | GCCTCCCCAGGAGGG[A/G]GAGATCAGGCACTTA | 114088 |
rs80304174 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036295 | CACTACAAATAAGAA[C/T]TTGTTTTTGTTTTTT | 114088 |
rs80316167 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993687 | GAGGCAGCTACACAG[C/T]GCTGCTTCATTTTGA | 114088 |
rs80346826 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056187 | ACAATAAGAAATTCA[A/G]ATATTCTAAAACTTG | 114088 |
rs111247774 | snp | A/G | 0.468349 | 0.121752 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054731 | GGCGCATGCCACTAC[A/G]CCTAGCTAATTTTTG | 114088 |
rs111278189 | snp | A/C | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998292 | AGCCCTGGTGTCATT[A/C]TAATCTGGATTTGAA | 114088 |
rs111278679 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061151 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 114088 |
rs111305025 | snp | C/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082523 | AGATGCAAAAGGCCA[C/T]ATATTTTATGATTCC | 114088 |
rs111373633 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081523 | TGACTCCAATTTACC[A/G]ACATCCCTAGGCGTC | 114088 |
rs111427732 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086067 | GAATCTTAGGAGAAA[A/C]ATGACTCAATTTCTC | 114088 |
rs111465765 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069097 | AATAAGAATAAAGGA[A/G]GAATTGAATGTGAGA | 114088 |
rs111474375 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051607 | AGGAGTATAATGCAA[C/T]TAGCTATTAATAAAT | 114088 |
rs111530481 | snp | A/G | 0.5 | 0 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975086 | TTCACATCAGGTTAA[A/G]TTTCATATGAGTAAA | 114088 |
rs111536929 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015239 | CAGAGCAACTCAGGA[A/G]AGAGTACACAATACA | 114088 |
rs111546782 | snp | A/T | 0.228547 | 0.249078 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048980 | CAGCATGAGACTCCA[A/T]CTCAAAAAAAAAAAA | 114088 |
rs111561233 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029168 | TCAATTCACCACAAA[G/T]ATTGGATAGCGATAA | 114088 |
rs111586814 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986887 | CTGTTTCTGTTCAGA[C/T]AGTCAGGTTTGGCCT | 114088 |
rs111620401 | snp | A/G | 0.029116 | 0.117091 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006951 | ACTCGCAGTTCCCAT[A/G]CCCAGTGAAGGGCCT | 114088 |
rs111634595 | snp | C/T | 0.156319 | 0.231784 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987945 | AGCAGGGACTACAGG[C/T]GTGAGCCATCACGCC | 114088 |
rs111636664 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032113 | AAATAATAATTTAAG[G/T]CTAAACATGCTGTTT | 114088 |
rs111645997 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077400 | TGTTTTTTTTTTTTT[C/T]TTTTTTTTTTGAGAC | 114088 |
rs111650381 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062573 | AATTATATGTAGATC[C/T]ATGTTTATAGGGGTT | 114088 |
rs111680095 | snp | A/C | 0.241053 | 0.24984 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061300 | CACCTGTAATCCCAG[A/C]TACTCAGGAGGCTGA | 114088 |
rs111711699 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005286 | TGACCTTGGTGCATA[C/T]TCAGGGCTCTTATAT | 114088 |
rs111725655 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079385 | TACTTCCTGCCCTCA[A/G]TGTAAGTAGAACTTC | 114088 |
rs111729443 | snp | C/G/T | 0.0154538 | 0.0865337 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024919 | TATTACAAGGTGTTT[C/G/T]GGAAACCTACAAGGT | 114088 |
rs111730710 | snp | A/C | 0.0135469 | 0.0811785 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022874 | GTTGACGCGGGCCAG[A/C]AGCTGGGCTTTTCTT | 114088 |
rs111734095 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033217 | GCCTCAGCCTCCTCC[C/T]GAGTAGCTGGGACTA | 114088 |
rs111740076 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091015 | CCATTTTAAAGTATC[C/T]ACAAAATCACTTTTT | 114088 |
rs111754369 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033448 | CATAAATCACGAAAA[C/T]ACTTTTGTCATACCA | 114088 |
rs111764212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988833 | GCCTGTAAGTCATCT[A/G]TACCACTTCACATTA | 114088 |
rs111816247 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061155 | TGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 114088 |
rs111818956 | snp | A/C | 0.029116 | 0.117091 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985861 | CTAGCTCATCCCCCT[A/C]ACCACGCACATGAAT | 114088 |
rs111842757 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047995 | TTACCAAATCCGTTA[A/G]GTGCATAGTAAATGC | 114088 |
rs111945202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071060 | TGGACTGATGGGGAC[A/G]ACAAAATAAGAATCC | 114088 |
rs111946206 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066082 | AGGAAGGAAGGAAGG[A/G]AGGAAGGAGGGAGGG | 114088 |
rs111965180 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046765 | GGCAAATTAAAAACT[C/T]TATACCTTCGTTTCC | 114088 |
rs112006898 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071268 | GTAATCCCAGCTACT[A/C]TGGAGGCTGAGGCAG | 114088 |
rs112016516 | snp | A/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036596 | TGTAAGTACTATGTA[A/T]ATAATTGTTACACTA | 114088 |
rs112016523 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068349 | CAAAAACAAAAACAA[A/C]AACAAAAAACAAACC | 114088 |
rs112066307 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049482 | AGAGTTACCATCCAT[C/T]TGTTTGTTCATTCCT | 114088 |
rs112125923 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997342 | CAAAAATTCTCTAGA[G/T]ATGAACCTTGTATGG | 114088 |
rs112147207 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025138 | GTTTGTATGTAAAGA[A/G]CAACAACAACCACAA | 114088 |
rs112158215 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026695 | AGTTGGGCACTGACT[C/T]TCTAAAAATATGCAC | 114088 |
rs112213272 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033255 | GTGCCACCACACCTG[G/T]CTAAATTTTGTATTT | 114088 |
rs112230659 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976975 | AAAAGAAAGAAAATA[A/C/T]AACTCACCTACATAA | 114088 |
rs112242826 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078826 | GGAGATCGAATGTAT[A/C]ACATGAGGACTGTAG | 114088 |
rs112256149 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093604 | CTCATCAGTATTCCG[C/G]CTGCGGCGTCTCCCC | 114088 |
rs112260130 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033668 | GTGATTTTCTGCTAG[C/T]TCTTTTGCTCTTCCT | 114088 |
rs112264147 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067222 | TGCCATTATTTAGCC[C/T]GTTTCTGAGGCCCCC | 114088 |
rs112305644 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022599 | CTTTATTATTCCTAT[A/G]TCCATTGCAGTTCCT | 114088 |
rs112317963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977542 | TGCTCACCATGGTGG[A/G]CTCTCAAATCCTGGT | 114088 |
rs112353453 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091724 | ACTGAACAAAAATTA[C/T]GTGTCCTTACTGTTT | 114088 |
rs112359559 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093960 | GTTAAGATTCCCCCA[C/T]GCCTCCTGCAATGCA | 114088 |
rs112359910 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090584 | AATTGTTACAAATAT[A/G]TTACTGATTCAGTGA | 114088 |
rs112370685 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987034 | AGCTGGTTCTATGCA[C/T]GGTGTGGTCTAGTCA | 114088 |
rs112404343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040386 | TGTCACCTTTTCTTC[C/T]GTTGCCTGTACCCGG | 114088 |
rs112433332 | in-del | -/CCAGGGACATTTAG | 0.0189856 | 0.0955633 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002548 | CAGCTTGGACCATAT[-/CCAGGGACATTTAG]ATGAACAAATGTTCA | 114088 |
rs112437325 | in-del | -/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060542 | ACGATCTCGGCTGAC[-/T]TGCAAGCTCCACTTC | 114088 |
rs112445153 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089057 | ATGCCATTATAATTC[A/G]CTGAGATTCGAAGAT | 114088 |
rs112461069 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980933 | GGGTCCAATTATCCT[A/G/T]CCAATGTCTGACTTG | 114088 |
rs112467362 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985494 | TGTACTTTGTCAATA[A/G]AGATCTCTTGAGTCT | 114088 |
rs112500608 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037081 | TGTAAACCAAGATTT[A/C/G]TCCATGATTAAGTCA | 114088 |
rs112522970 | snp | G/T | 0.0260255 | 0.111165 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090829 | TCTTAAATCCTGGCC[G/T]CAAGAGATCTGACCG | 114088 |
rs112606010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023758 | AATTTTGCATATATA[C/T]GCATAATCTGAAAAA | 114088 |
rs112610112 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030868 | AGAAAGATTCGAGGC[C/T]GGGCGTGGTGGCTCA | 114088 |
rs112618455 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073948 | GCTGGCTTGTACTGA[C/T]TTCCAAACATCAAGG | 114088 |
rs112649796 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086712 | ATGGAGGAGGGTGAG[C/T]TGAACAGGTGACAGG | 114088 |
rs112665441 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023972 | TAATCAACTGGTAGG[C/T]ATTTAGTAATTGTTT | 114088 |
rs112762683 | snp | C/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026690 | TACAAAGTTGGGCAC[C/T]GACTCTCTAAAAATA | 114088 |
rs112763630 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983126 | CTTGTACCTTTACCC[A/C]CATTTAGTGCTCATA | 114088 |
rs112778856 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083319 | TGCATTGGTGTAATC[A/T]TGGCTCACTGTAATC | 114088 |
rs112810369 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092551 | CTATCTTCACTGCTC[C/T]ATCTCATCCTTGGGT | 114088 |
rs112835619 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980424 | AGCAGAGCACAGGAA[C/T]TTGTGTCATTCATTT | 114088 |
rs112854448 | in-del | -/TTCA/TTCATTCA/TTCATTCATTCA | 0.391099 | 0.266607 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097515 | TCATTCATTCATTCA[-/TTCA/TTCATTCA/TTCATTCATTCA]ACAAGTGCTGAGTTC | 114088 |
rs112865655 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028583 | ATGCAAATATGTAGT[A/G]TGTGTTTTCATCACG | 114088 |
rs112882292 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000219 | TATTATTAGCAATAA[A/G]CAATGATGGTAATAA | 114088 |
rs112894641 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090565 | AGTAGCATGAACACA[A/G]AATAATTGTTACAAA | 114088 |
rs112914032 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095776 | CGTCCCTCGTTTCCT[A/G]AAGAGCATGTATAAA | 114088 |
rs112919592 | in-del | -/TCATTTGGTAGTAACTT | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993075 | TCTGAGTGCCAGACC[-/TCATTTGGTAGTAACTT]TCATTTGGTAGTATC | 114088 |
rs113000402 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060657 | TATTTTTAGTAGAAA[C/T]GGGGTTTCGCCGTGT | 114088 |
rs113006546 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075233 | AAGTTTGTCTACCCT[A/G]TTTAGCCACTGCTAT | 114088 |
rs113057083 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977855 | CAATTTCCGTGTATC[C/T]CCAAACCTCAATGGA | 114088 |
rs113094847 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066349 | CATCTTTGCAAACCC[A/G]AAGGTCAGTACTTTG | 114088 |
rs113120856 | snp | C/T | 0.0295035 | 0.117819 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983210 | GCATAACATTAAACA[C/T]TACAGGCATCTTTTC | 114088 |
rs113125682 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977629 | TTGTGTTCCTTATAA[C/G]TGAAGACACAGGCCT | 114088 |
rs113133369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080214 | AAGGTAATGTCTATC[A/G]AAAGCCAATGTTAAA | 114088 |
rs113154711 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084456 | AGTGTGTAAACATCA[C/T]TCAGCTTCATACTGC | 114088 |
rs113159461 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078066 | GTGGTCTTATCAGAT[G/T]AGCCAGTGGTCTCAT | 114088 |
rs113178358 | in-del | -/TG | 0.0603597 | 0.1629 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080386 | GGGTGTCTGAGGGCA[-/TG]TGGAAGAGTCCCCAG | 114088 |
rs113228488 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090919 | AGTGACTATTGAAAC[C/T]CCAGGAATTCAAGGA | 114088 |
rs113285535 | snp | A/C | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051147 | TTTTAGTAAGGAATT[A/C]ATATGTTCTGGTTCA | 114088 |