SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15191 | snp | A/C | 0 | 0 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179520 | AACTCCCCCACGGAC[A/C]CCTTCAACCGGCAGA | 10277 |
rs1046277 | snp | C/T | 0.23031 | 0.249223 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180036 | CCGCAGCGAAGCTGC[C/T]GTTCATGTGTTGGAG | 10277 |
rs1074461 | snp | A/G | 0.472896 | 0.113214 | intron-variant | UBE4B | GRCh38.p7 | 1:10143387 | TTTAGACTGAGCCTC[A/G]CTCTATTGCCCAGGC | 10277 |
rs1801442 | snp | C/G/T | 1.64749e-05 | 0.00287005 | missense, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171204 | GTGGNCCCCAAGTGC[C/G/T]GTGACCTGAAAGTTG | 10277 |
rs1830501 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10136641 | CCTTAAACTTCTggc[C/G]gggcatggtggctca | 10277 |
rs1973936 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137998 | ggagtgcagtggtac[C/G]atctcagctcggtgc | 10277 |
rs2004601 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | UBE4B | GRCh38.p7 | 1:10146302 | actaaaaatacaaaa[A/T]ttaactgggtgtggt | 10277 |
rs2038353 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10169742 | GCATAAggccaagca[C/T]ggtggctcatgcctg | 10277 |
rs2180184 | snp | A/G | 0.453087 | 0.145793 | intron-variant | UBE4B | GRCh38.p7 | 1:10175888 | actgtactacatgcc[A/G]caaaatggtacactt | 10277 |
rs2273297 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10179741 | CATGAGAGGGAGGGA[C/T]TGGATGTCTGCAGGG | 10277 |
rs2273298 | snp | A/G | 0.323926 | 0.23882 | intron-variant | UBE4B | GRCh38.p7 | 1:10158319 | TTGGAAAGCAAGAAA[A/G]TACATATCCCTCAGT | 10277 |
rs2273299 | snp | C/T | 0.323534 | 0.238941 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158381 | TACCGGAGCCACCAG[C/T]GAGTTTTATGACAAG | 10277 |
rs2273300 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | UBE4B | GRCh38.p7 | 1:10161343 | TCTGCCTCCACACAC[A/G]GGCAGAGCTGCTTTG | 10277 |
rs2295294 | snp | A/T | 0.486288 | 0.0816578 | intron-variant | UBE4B | GRCh38.p7 | 1:10130826 | AGGGTAAGTGTTCAG[A/T]AAACAAATCCAGAGG | 10277 |
rs3762290 | snp | C/T | 0.474091 | 0.11083 | intron-variant | UBE4B | GRCh38.p7 | 1:10117732 | CCTAAGTTCCTAGTA[C/T]TGTGCCTGGCACATG | 10277 |
rs3790487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10169475 | TCCATGGCTCTTGCA[C/T]TGAAATCTGTTTATG | 10277 |
rs3818158 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10151782 | TCTCTGATGATTCAG[C/G]AGGAACTACTGAAAG | 10277 |
rs4265433 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBE4B | GRCh38.p7 | 1:10065497 | ATTTCCCCACGCTGC[A/G]GGGGTAGTTTCGGCC | 10277 |
rs4333851 | snp | A/G | 0.492237 | 0.0618148 | intron-variant | UBE4B | GRCh38.p7 | 1:10086121 | GGACTACAGGCGCCC[A/G]CCACCACGCCAGGCT | 10277 |
rs4360526 | snp | C/T | 0.448836 | 0.15154 | intron-variant | UBE4B | GRCh38.p7 | 1:10086128 | AGGCGCCCGCCACCA[C/T]GCCAGGCTAATTTTT | 10277 |
rs4388708 | snp | C/T | 0.102726 | 0.202016 | intron-variant | UBE4B | GRCh38.p7 | 1:10088487 | TTCAAGAAATTCTCC[C/T]GCCTCAGCCTCCTGA | 10277 |
rs4415569 | snp | C/T | 0.16028 | 0.233346 | intron-variant | UBE4B | GRCh38.p7 | 1:10134449 | CCCGGGAGGCGGAGG[C/T]TGTAGTGAGCGAGGA | 10277 |
rs4442371 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10056311 | AAGGGGAAACTGAGC[C/T]TAAGAGGAAGATTAA | 10277 |
rs4443893 | snp | A/T | 0.223591 | 0.248601 | intron-variant | UBE4B | GRCh38.p7 | 1:10054072 | ATATTAGATTTTTTT[A/T]AAAAAAAAAGACAGG | 10277 |
rs4500322 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10158023 | ATTTGAGGTGCCATA[A/G]AATTTCTGTAAATTA | 10277 |
rs4543799 | snp | A/G | 0.466124 | 0.127311 | intron-variant | UBE4B | GRCh38.p7 | 1:10114131 | GTAAAGATGTGAGAA[A/G]AATGGGGCTTATTAT | 10277 |
rs4846193 | snp | G/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10150258 | CGTGATTTTGATTGG[G/T]ATGAAATTTTAAAAG | 10277 |
rs4846195 | snp | C/T | 0.232359 | 0.249377 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181529 | AGATTCTTCCTCAGG[C/T]CGGGCCCGGTGGCTC | 10277 |
rs4846196 | snp | A/G | 0.499424 | 0.0169631 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181582 | gggaggctgaggcgg[A/G]tggatcacctgacgt | 10277 |
rs5772395 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082633 | TATTAAGAAGGCGAC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs5772396 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115165 | ACTTTAATACCATAC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs6541075 | snp | A/T | 0.490175 | 0.0693959 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032712 | GAGTCGTCCCTCCCC[A/T]TGCCAGCCTACCTGG | 10277 |
rs6541076 | snp | C/G | 0.451856 | 0.147493 | intron-variant | UBE4B | GRCh38.p7 | 1:10040833 | ccatgttggcttggc[C/G]ggtctcaaactcttg | 10277 |
rs6541077 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE4B | GRCh38.p7 | 1:10084843 | GCTGGGATTACAAGC[A/G]CCCGCCACCATTCCT | 10277 |
rs6541078 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10138883 | ctattctgttaatgt[A/G]gttgaattatatcag | 10277 |
rs6541079 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | UBE4B | GRCh38.p7 | 1:10175629 | gcactccagcctggg[C/T]gacagagcgagactc | 10277 |
rs6541080 | snp | A/G | 0.49907 | 0.0215454 | intron-variant | UBE4B | GRCh38.p7 | 1:10175981 | acccttaaagcagtc[A/G]ctgtctagaccccct | 10277 |
rs6657925 | snp | C/G | 0.0146672 | 0.084371 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031232 | gtagctgggattaca[C/G]gtgcccgccaccacg | 10277 |
rs6659436 | snp | C/T | 0.257454 | 0.249889 | intron-variant | UBE4B | GRCh38.p7 | 1:10159144 | ATGAAATCTTAGTTC[C/T]TGAATGTTGGAAGGA | 10277 |
rs6664155 | snp | C/T | 0.154329 | 0.23097 | intron-variant | UBE4B | GRCh38.p7 | 1:10120411 | gcctgtaatcccagc[C/T]acctgggaggctgag | 10277 |
rs6665885 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10154661 | ctggccaaaatggtg[A/C]aaccccgtctctact | 10277 |
rs6667049 | snp | C/T | 0.462363 | 0.131916 | intron-variant | UBE4B | GRCh38.p7 | 1:10161789 | ATGGAAAGCACGTGC[C/T]GTGCCAGTACCAGTG | 10277 |
rs6669051 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | UBE4B | GRCh38.p7 | 1:10116843 | tgagactagaaccca[C/T]gtctggttactccta | 10277 |
rs6671289 | snp | A/G | 0.463774 | 0.129618 | intron-variant | UBE4B | GRCh38.p7 | 1:10135882 | TTATTTAACCTATCT[A/G]AAGTGAATTCTGGTG | 10277 |
rs6673887 | snp | C/T | 0.3748 | 0.216622 | intron-variant | UBE4B | GRCh38.p7 | 1:10133763 | aaaatatacaaaagt[C/T]aTctgggcatggtgg | 10277 |
rs6676280 | snp | A/G | 0.49334 | 0.057322 | intron-variant | UBE4B | GRCh38.p7 | 1:10092824 | taagagtgaaactct[A/G]tctcaaaaaaaaaaa | 10277 |
rs6677855 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10137426 | gagttctgaaccctg[A/G]atatttcactctgtt | 10277 |
rs6678222 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10098284 | taaatatcatctacc[A/G]tattgcatgttaaaa | 10277 |
rs6678519 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10068419 | cagtggtgcgatctc[A/G]gctcactgtgacctc | 10277 |
rs6679112 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10067642 | ttttttttgagaccc[A/G]gctctcaccgggttg | 10277 |
rs6679221 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10067789 | ctggagtgcaatggc[A/G]tgatctcagctcact | 10277 |
rs6681003 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10040742 | cctgcctcagcctcc[C/T]gagtagctgggatta | 10277 |
rs6682295 | snp | A/G | 0.194902 | 0.243853 | intron-variant | UBE4B | GRCh38.p7 | 1:10179139 | CAGCCTGCCGTCCTC[A/G]CCACGGAGCCTGTGG | 10277 |
rs6685910 | snp | A/T | 0.376592 | 0.215579 | intron-variant | UBE4B | GRCh38.p7 | 1:10135912 | GATTCATAGCAAAAA[A/T]TATAATACTGTTGTT | 10277 |
rs6687550 | snp | C/T | 0.159292 | 0.232964 | intron-variant | UBE4B | GRCh38.p7 | 1:10137554 | gacataccccttctt[C/T]cctggactgtgaaaa | 10277 |
rs6688765 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10040786 | ccatgcctggctaat[G/T]tttttgtatttttat | 10277 |
rs6688779 | snp | A/G | 0.160609 | 0.233472 | intron-variant | UBE4B | GRCh38.p7 | 1:10136495 | cttaaaaaaaaaaaa[A/G]aaaaaaGATTGTGAT | 10277 |
rs6691957 | snp | A/T | 0.160609 | 0.233472 | intron-variant | UBE4B | GRCh38.p7 | 1:10136676 | tgtaatcccagcact[A/T]tgggaggccaaggag | 10277 |
rs6692491 | snp | A/G | 0.476833 | 0.105105 | intron-variant | UBE4B | GRCh38.p7 | 1:10167836 | cctcgtgattcgccc[A/G]ccttggcttcgcaaa | 10277 |
rs6693010 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10079307 | gggattacaggcatg[C/T]gccaccacgcccggc | 10277 |
rs6693449 | snp | A/G | 0.490231 | 0.0692021 | intron-variant | UBE4B | GRCh38.p7 | 1:10037614 | CCAGTCTGGAATGCA[A/G]TGGCATGATCTTGGC | 10277 |
rs6693686 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | UBE4B | GRCh38.p7 | 1:10067975 | ccttgtgatccgccc[A/G]cctcagcctcccaaa | 10277 |
rs6696978 | snp | A/G | 0.300169 | 0.244914 | intron-variant | UBE4B | GRCh38.p7 | 1:10149499 | ATTAACAGTGCAGAT[A/G]ATGTATTCCTTGAAA | 10277 |
rs6697968 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10079457 | gagccaccgcacccg[A/G]cctcaaaatttactt | 10277 |
rs6700518 | snp | A/T | 0.179105 | 0.239737 | intron-variant | UBE4B | GRCh38.p7 | 1:10150515 | TATAGTTAATATAAC[A/T]TGCTACAGCCAGTAA | 10277 |
rs6701103 | snp | A/G | 0.165853 | 0.235413 | intron-variant | UBE4B | GRCh38.p7 | 1:10080195 | gggaggccgagatgg[A/G]gggatcatgaggtca | 10277 |
rs6702986 | snp | C/G | 0.0629771 | 0.165899 | intron-variant | UBE4B | GRCh38.p7 | 1:10090213 | cagcctcagcctcct[C/G]ggctcaggtgaccca | 10277 |
rs7354817 | snp | A/T | 0.486855 | 0.0799975 | intron-variant | UBE4B | GRCh38.p7 | 1:10175654 | agactccgtctcaaa[A/T]aaataaataaataaa | 10277 |
rs7355148 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | UBE4B | GRCh38.p7 | 1:10175909 | gtagtacagtcacag[C/T]gttgcacagccacca | 10277 |
rs7412246 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10163223 | agcatgtaccaccac[A/G]cttggctaattaaaa | 10277 |
rs7414561 | snp | A/G/T | 6.5895e-05 | 0.00573967 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137107 | GCCGAAATTCCCTAC[A/G/T]GAGTGCTTCTTTCTC | 10277 |
rs7416007 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10125132 | ttgtgtctggaaaaa[A/G]gaaaaagaaaaagaa | 10277 |
rs7418410 | snp | C/T | 0.495596 | 0.0467178 | intron-variant | UBE4B | GRCh38.p7 | 1:10176344 | acctgttttcagtta[C/T]tttgggtctacactt | 10277 |
rs7512714 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10131436 | gttgcagtgagccaa[G/T]atcacgccactgcac | 10277 |
rs7517298 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032919 | GGCTGCCACGTCCCG[A/G]CGCCAGAAGCCCCGC | 10277 |
rs7522444 | snp | C/G/T | 0.128162 | 0.220096 | intron-variant | UBE4B | GRCh38.p7 | 1:10156332 | gcactcttgacctcc[C/G/T]gggctcaagtgatcc | 10277 |
rs7524177 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10060735 | GCTGTGTATTTTAGA[A/G]TCCCTAGTGAGCTAG | 10277 |
rs7528979 | snp | C/T | 0.494484 | 0.0522255 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033399 | AGTGGCGCCTTAAGA[C/T]AACCCTGTAGCAGCA | 10277 |
rs7529458 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10061073 | TGTTTTCTGTTTTTT[C/T]TTTTATCTCAAAAGA | 10277 |
rs7531071 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10134281 | tttgggaggccgaga[C/T]gggcgtatcacctga | 10277 |
rs7538285 | snp | A/G | 0.118933 | 0.212888 | intron-variant | UBE4B | GRCh38.p7 | 1:10074469 | tgcaccaaaaccttt[A/G]cagcagaacttccgg | 10277 |
rs7538883 | snp | A/G | 0.3752 | 0.216391 | intron-variant | UBE4B | GRCh38.p7 | 1:10135475 | TGGGCATGGTGGCAC[A/G]CGCCTGTAATCCCAG | 10277 |
rs7539725 | snp | A/G | 0.465683 | 0.126415 | intron-variant | UBE4B | GRCh38.p7 | 1:10065349 | AGTGGCGGGAGGAGC[A/G]TGCGGGGGAGGAAGG | 10277 |
rs7540431 | snp | A/G | 0.498852 | 0.0239341 | intron-variant | UBE4B | GRCh38.p7 | 1:10175454 | caggagatcgagacc[A/G]tcctggctaacacgg | 10277 |
rs7540888 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10102699 | tacaggtgtgagcca[C/G]cacgcccggccATCT | 10277 |
rs7541780 | snp | C/T | 0.3748 | 0.216622 | intron-variant | UBE4B | GRCh38.p7 | 1:10135548 | TCATGACCAGCCTGA[C/T]CACCATGGTGAAACC | 10277 |
rs7542626 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066056 | ctccttccctccccc[A/C]ctccttccctctctc | 10277 |
rs7546283 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | UBE4B | GRCh38.p7 | 1:10097760 | ggttgctgtgacctg[A/G]gatcgcaccgctgca | 10277 |
rs7546642 | snp | A/G | 0.0879473 | 0.190365 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178712 | AGGGATCAAATCCAC[A/G]ATAGCAATAGAAAAA | 10277 |
rs7549318 | snp | C/T | 0.499913 | 0.00658888 | intron-variant | UBE4B | GRCh38.p7 | 1:10175511 | aaaaaattagccagg[C/T]gtggtggcgggcgcc | 10277 |
rs7550904 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049805 | tgagatgggagaatc[A/G]cttgagcccggcagg | 10277 |
rs7553655 | snp | A/G | 0.32627 | 0.238082 | intron-variant | UBE4B | GRCh38.p7 | 1:10175434 | aggcgggcggatcac[A/G]aggtcaggagatcga | 10277 |
rs7553668 | snp | A/G/T | 0.500158 | 0.0507834 | intron-variant | UBE4B | GRCh38.p7 | 1:10175479 | acacggtgaaacccc[A/G/T]tctctactaaaaata | 10277 |
rs7553760 | snp | A/G | 0.499218 | 0.0197529 | intron-variant | UBE4B | GRCh38.p7 | 1:10175508 | tacaaaaaattagcc[A/G]ggcgtggtggcgggc | 10277 |
rs7555121 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090200 | ttgtggctcactgca[A/G]cctcagcctcctggg | 10277 |
rs7556506 | snp | C/G/T | 0.291493 | 0.246533 | intron-variant | UBE4B | GRCh38.p7 | 1:10175462 | cgagaccgtcctggc[C/G/T]aacacggtgaaaccc | 10277 |
rs9430244 | snp | A/G | 0.257454 | 0.249889 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095225 | AGTTTTAGGCATTAG[A/G]TGTAGCTCTGTTACT | 10277 |
rs9430245 | snp | A/T | 0.451608 | 0.147832 | intron-variant | UBE4B | GRCh38.p7 | 1:10097052 | TCAAAAAAAAAAAAA[A/T]AATAATAATAATAAT | 10277 |
rs9430246 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173712 | CAGGGCTCTTCCATC[A/G]TTGCCGTAGAGAGAC | 10277 |
rs9662454 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10136749 | acatggtgaaacctc[A/G]tctctcctaaaaatg | 10277 |
rs9728230 | snp | C/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10139625 | cttgtgtcagttttt[C/G]taaagtttgaaaatg | 10277 |
rs9782879 | snp | A/G | 0.179744 | 0.239925 | intron-variant | UBE4B | GRCh38.p7 | 1:10171927 | aaaacaaaaGTAAAG[A/G]GCAGGTTTGGCGCTC | 10277 |
rs9782923 | snp | C/G | 0.179105 | 0.239737 | intron-variant | UBE4B | GRCh38.p7 | 1:10171754 | agtgtggtggtgcat[C/G]cctgtaatcacagct | 10277 |
rs9782938 | snp | C/G | 0.17461 | 0.238362 | intron-variant | UBE4B | GRCh38.p7 | 1:10172066 | CCTAGTCTCCTGCTA[C/G]AGTGCTGTTATTTTT | 10277 |
rs9782997 | snp | C/T | 0.180383 | 0.240111 | intron-variant | UBE4B | GRCh38.p7 | 1:10173398 | gaggcaggagaatgg[C/T]gtgaacccaggaggc | 10277 |
rs9783053 | snp | A/G | 0.354665 | 0.227036 | intron-variant | UBE4B | GRCh38.p7 | 1:10173698 | GGTGTGGAAAGCCCC[A/G]GGGCTCTTCCATCGT | 10277 |
rs9804105 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10136852 | ttgaacctgggaggc[A/G]gaatttgcagtaagc | 10277 |
rs9919194 | snp | A/G | 0.492775 | 0.059668 | intron-variant | UBE4B | GRCh38.p7 | 1:10048049 | gacgagggtctccct[A/G]tgttgcctaggctgg | 10277 |
rs10127541 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | UBE4B | GRCh38.p7 | 1:10105258 | ttcagttagtgcagg[A/G]agttcctatatatac | 10277 |
rs10864442 | snp | A/C | 0.49104 | 0.0793184 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100196 | gggtttcaccatgtt[A/C]gccaggatggtctcg | 10277 |
rs10864443 | snp | C/G | 0.46703 | 0.124089 | intron-variant | UBE4B | GRCh38.p7 | 1:10150913 | atgcctgtaatccca[C/G]cattttgggaggtcg | 10277 |
rs10864444 | snp | C/T | 0.466927 | 0.124269 | intron-variant | UBE4B | GRCh38.p7 | 1:10150916 | cctgtaatcccacca[C/T]tttgggaggtcgagg | 10277 |
rs10864445 | snp | C/T | 0.465788 | 0.126237 | intron-variant | UBE4B | GRCh38.p7 | 1:10150926 | caccattttgggagg[C/T]cgaggcgggcggatc | 10277 |
rs10864446 | snp | C/T | 0.465892 | 0.126058 | intron-variant | UBE4B | GRCh38.p7 | 1:10150932 | tttgggaggtcgagg[C/T]gggcggatcacgagg | 10277 |
rs10864447 | snp | A/C | 0.476314 | 0.106217 | intron-variant | UBE4B | GRCh38.p7 | 1:10166972 | acacacacacacaca[A/C]aaaaaaaaaattagc | 10277 |
rs11121515 | snp | C/T | 0.278399 | 0.248382 | intron-variant | UBE4B | GRCh38.p7 | 1:10065707 | CTGAATGTTTTCCCA[C/T]GGTAGATGTAGTGGG | 10277 |
rs11121516 | snp | C/T | 0.4021 | 0.198407 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094516 | TTGGCTCACTGCAAC[C/T]TCCGCCTCCCGGGTT | 10277 |
rs11121517 | snp | C/T | 0.217851 | 0.247924 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094578 | agctgggactacagg[C/T]gcccgccaccacgcc | 10277 |
rs11121519 | snp | C/T | 0.195214 | 0.243923 | intron-variant | UBE4B | GRCh38.p7 | 1:10098987 | tcacacctgtaatcc[C/T]agcacttttgggagg | 10277 |
rs11121520 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107685 | tgggttcaagtgatt[C/T]tcctgcctcagactc | 10277 |
rs11121521 | snp | A/G | 0.3742 | 0.216966 | intron-variant | UBE4B | GRCh38.p7 | 1:10138159 | ctggagtccaatggc[A/G]tgatctcggctcact | 10277 |
rs11121522 | snp | C/T | 0.431325 | 0.172108 | intron-variant | UBE4B | GRCh38.p7 | 1:10148710 | TTTGGGAGGCCAAGA[C/T]GGGTGGATCACTTGA | 10277 |
rs11121523 | snp | A/T | 0.299411 | 0.245069 | intron-variant | UBE4B | GRCh38.p7 | 1:10154384 | gatcTAAAAAAATTT[A/T]AAAAAAAAAGAGTGG | 10277 |
rs11121524 | snp | C/G | 0.316726 | 0.240931 | intron-variant | UBE4B | GRCh38.p7 | 1:10172476 | GACAGAGGCATGATC[C/G]ATGTCCAGGCAGCCT | 10277 |
rs11121525 | snp | C/T | 0.352938 | 0.227824 | intron-variant | UBE4B | GRCh38.p7 | 1:10174471 | TTTGGGGAGCCGAGG[C/T]GGGCAGATCACCTGA | 10277 |
rs11582326 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160837 | agttccagctactta[A/G]gaggctgaggcagga | 10277 |
rs11584736 | snp | A/C | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10087418 | gttcatttgtcaaaa[A/C]taagggattagcctg | 10277 |
rs11585670 | snp | A/C | 0.0737376 | 0.17729 | intron-variant | UBE4B | GRCh38.p7 | 1:10120850 | CAAAAAATAATAATA[A/C]TACTAAATAAATAAA | 10277 |
rs11586245 | snp | G/T | 0.00938946 | 0.0678717 | intron-variant | UBE4B | GRCh38.p7 | 1:10053581 | gtaagcgtgtaccgt[G/T]gtggtttgctgcacc | 10277 |
rs11589489 | snp | A/G | 0.040671 | 0.13668 | intron-variant | UBE4B | GRCh38.p7 | 1:10073626 | aagagaggctgaggc[A/G]tgagaattgcttaaa | 10277 |
rs11590663 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10049039 | CATGAGGTTTTGGGC[C/T]TGAAGAGTTCCAAAT | 10277 |
rs11799711 | snp | C/T | 0.0659966 | 0.169242 | intron-variant | UBE4B | GRCh38.p7 | 1:10111086 | acacacacacacaca[C/T]acacacaGTCTTTCC | 10277 |
rs11801417 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10148657 | aaaaaatcaagaaaa[A/G]ggccaggtgtggtgg | 10277 |
rs11801988 | snp | A/G | 0.110167 | 0.207236 | intron-variant | UBE4B | GRCh38.p7 | 1:10093095 | CACATACTATACTAT[A/G]CTACAGATACAGTTT | 10277 |
rs11802173 | snp | A/T | 0.0629771 | 0.165899 | intron-variant | UBE4B | GRCh38.p7 | 1:10088389 | ttttaaatttatttt[A/T]tttttttttgagatg | 10277 |
rs11803995 | snp | A/G | 0.157642 | 0.232314 | intron-variant | UBE4B | GRCh38.p7 | 1:10034255 | TTCCAGTTATATTCT[A/G]GTACTTAATAGACCA | 10277 |
rs11804193 | snp | A/C | 0.410061 | 0.192043 | intron-variant | UBE4B | GRCh38.p7 | 1:10043073 | ggactgcagtggctc[A/C]atgtcagctcactgc | 10277 |
rs11804755 | snp | A/G | 0.144632 | 0.226711 | intron-variant | UBE4B | GRCh38.p7 | 1:10038929 | gctgggtgtgatggt[A/G]cgcacctgtaatccc | 10277 |
rs11804805 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | UBE4B | GRCh38.p7 | 1:10078095 | gctcactgcaacctc[C/T]gtcacccgggttcaa | 10277 |
rs11805696 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | UBE4B | GRCh38.p7 | 1:10043496 | cagtggcgcgatctc[A/G]gctcactgcaagctc | 10277 |
rs11806008 | snp | A/G | 0.309648 | 0.24278 | intron-variant | UBE4B | GRCh38.p7 | 1:10174530 | ACATGGTGAAACCCT[A/G]TTTCTACTAAAAATA | 10277 |
rs11806062 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10041348 | ttctttttttttttt[G/T]tttttgatggagttt | 10277 |
rs11806378 | snp | A/C | 0.0637235 | 0.166737 | intron-variant | UBE4B | GRCh38.p7 | 1:10053475 | tatttaatttttttg[A/C]gatggaattttgctc | 10277 |
rs11807005 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049763 | ggtgtggtggcatgc[A/G]cctgtggtcccagct | 10277 |
rs11807784 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | UBE4B | GRCh38.p7 | 1:10053332 | ttttttgtattttta[G/T]tagagacggggtttc | 10277 |
rs11808311 | snp | A/G | 0.160938 | 0.233598 | intron-variant | UBE4B | GRCh38.p7 | 1:10112592 | tttagtagagacagg[A/G]ttttatcacattggc | 10277 |
rs11809750 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | UBE4B | GRCh38.p7 | 1:10052368 | tgagccactgggcct[A/G]gtcAGTGGTGATTTA | 10277 |
rs11810806 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | UBE4B | GRCh38.p7 | 1:10172725 | gacagctttattgag[C/G]tataactcacataTG | 10277 |
rs12025312 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10059763 | ACAGCTGTAGGCATC[C/T]GAAGTTGTTGAGCGT | 10277 |
rs12030552 | snp | A/C | 0.190833 | 0.242898 | intron-variant | UBE4B | GRCh38.p7 | 1:10036027 | gggattacaggtgtg[A/C]gccaccgcgcccggc | 10277 |
rs12035441 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10150595 | ggctgggtgcaatgg[C/T]tcatgcctgtaatcc | 10277 |
rs12038643 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10046673 | TGACTTTATTTTCTG[A/G]AGAGTTTTTCTGTGT | 10277 |
rs12044437 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10133204 | ATCCTTCCTTGACTA[A/G]TAATAAATAATGAAT | 10277 |
rs12045943 | snp | A/G | 0.194278 | 0.243711 | intron-variant | UBE4B | GRCh38.p7 | 1:10142997 | cctgtagtcgccact[A/G]ctcaggaggctgagg | 10277 |
rs12058322 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073948 | ttttttttttttgga[A/G]atgaggtctcactgg | 10277 |
rs12058944 | snp | A/T | 0.122064 | 0.214785 | intron-variant | UBE4B | GRCh38.p7 | 1:10147533 | TCTCAGTTTCCAGAT[A/T]GCATTTATATAGATT | 10277 |
rs12059587 | snp | C/T | 0.00769219 | 0.061538 | intron-variant | UBE4B | GRCh38.p7 | 1:10127802 | caaggcactcataat[C/T]tactgCAAAAATAAG | 10277 |
rs12060254 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112623 | caggctggtcttgca[C/T]gcctgacctcaagtg | 10277 |
rs12068865 | snp | A/G | 0.184838 | 0.241358 | intron-variant | UBE4B | GRCh38.p7 | 1:10081288 | tggtctccaactccc[A/G]atgtcagatgatctg | 10277 |
rs12070814 | snp | C/T | 0.3742 | 0.216966 | intron-variant | UBE4B | GRCh38.p7 | 1:10140516 | GCTTATAATATCAAT[C/T]ACTGAGAGAAGCTTA | 10277 |
rs12074007 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114081 | aaaaaaaaaaaaaga[A/G]aaaaaaaaaaaaaGA | 10277 |
rs12074936 | snp | C/T | 0.353587 | 0.22753 | intron-variant | UBE4B | GRCh38.p7 | 1:10173977 | GCACCTGGCTTGGGT[C/T]GTAGACAGCAGTTTC | 10277 |
rs12076005 | snp | A/C | 0.120326 | 0.21374 | intron-variant | UBE4B | GRCh38.p7 | 1:10149361 | GAGCTATGTTGCAAA[A/C]CTCCATTTCATGCCT | 10277 |
rs12076922 | snp | G/T | 0.349233 | 0.229462 | intron-variant | UBE4B | GRCh38.p7 | 1:10105243 | TAATTTTGGAATAGT[G/T]TCAGTTAGTGCAGGG | 10277 |
rs12078482 | snp | C/G | 0.180383 | 0.240111 | intron-variant | UBE4B | GRCh38.p7 | 1:10173885 | ACAAAGGAATGCTTT[C/G]AGCGGCCTTTGTTTG | 10277 |
rs12078483 | snp | A/G | 0.180064 | 0.240019 | intron-variant | UBE4B | GRCh38.p7 | 1:10173889 | AGGAATGCTTTGAGC[A/G]GCCTTTGTTTGGTGA | 10277 |
rs12078622 | snp | A/G | 0.471292 | 0.116318 | intron-variant | UBE4B | GRCh38.p7 | 1:10114079 | CAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 10277 |
rs12080683 | snp | G/T | 0.196771 | 0.244268 | intron-variant | UBE4B | GRCh38.p7 | 1:10123772 | cgttgttgttttgtt[G/T]tgttttgttttgttt | 10277 |
rs12082994 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | UBE4B | GRCh38.p7 | 1:10034389 | GAAGCAAATGACTTT[C/G]TAAACTCTCTCCTGT | 10277 |
rs12087114 | snp | C/T | 0.121717 | 0.214577 | intron-variant | UBE4B | GRCh38.p7 | 1:10162092 | caatccccgcttctc[C/T]ggttgaagcgatttt | 10277 |
rs12088302 | snp | C/T | 0.0108105 | 0.0727212 | intron-variant | UBE4B | GRCh38.p7 | 1:10043357 | GTTTTTCAATCATTT[C/T]TGAGATGTACTCTCC | 10277 |
rs12092513 | snp | C/T | 0.382085 | 0.212258 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171405 | AGTGGCCAGGGAACT[C/T]GTCTGGTGTAAATGA | 10277 |
rs12097972 | snp | C/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10120570 | AGTTTACAGGCCAgg[C/G]tcatgcctgtaatcc | 10277 |
rs12119603 | snp | A/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10155084 | GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG | 10277 |
rs12122985 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | UBE4B | GRCh38.p7 | 1:10155149 | AGAACTGGGCCTGTT[C/G]CCTATAAGACGAGTG | 10277 |
rs12129751 | snp | A/T | 0.160938 | 0.233598 | intron-variant | UBE4B | GRCh38.p7 | 1:10175678 | aaataaataaataaa[A/T]aagaaaataaaaaaa | 10277 |
rs12137054 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119013 | tcagcctcctgagta[A/G]ctgggactacaggcg | 10277 |
rs12137235 | snp | C/T | 0 | 0 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10030987 | ccttgaaaacatatg[C/T]taagtgaaggaagcc | 10277 |
rs12137598 | snp | A/C | 0.140581 | 0.224783 | intron-variant | UBE4B | GRCh38.p7 | 1:10166970 | acacacacacacaca[A/C]aaaaaaaaaaaatta | 10277 |
rs12142943 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062038 | cctcagcttcctgag[G/T]atctgggattacagg | 10277 |
rs12144133 | snp | G/T | 0.458545 | 0.137872 | intron-variant | UBE4B | GRCh38.p7 | 1:10144128 | GTGATGGGGAAGCCT[G/T]TTACTGCAGAGACAG | 10277 |
rs12217086 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10176825 | gagtctccctctgtt[A/G]cccaggctggagtgc | 10277 |
rs12239536 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10084618 | AAGTAGTAGGGTTGA[C/T]TGCATTGATTTGGGA | 10277 |
rs12402509 | snp | A/T | 0.444444 | 0.157135 | intron-variant | UBE4B | GRCh38.p7 | 1:10150875 | aagaaaaaaaaaaaa[A/T]aaTAggctgggcgca | 10277 |
rs12406448 | snp | C/T | 0.130008 | 0.219321 | intron-variant | UBE4B | GRCh38.p7 | 1:10046717 | GGGTCAGATCTGAAG[C/T]GGACATTGGAGGCTA | 10277 |
rs12564842 | snp | G/T | 0.188 | 0.24219 | intron-variant | UBE4B | GRCh38.p7 | 1:10035428 | ttgaggcggagtctc[G/T]ctctgtcgcccaggc | 10277 |
rs12727488 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111748 | gatcacttgaggtca[G/T]gagttcaagacaagc | 10277 |
rs12733312 | snp | C/T | 0.391583 | 0.206044 | intron-variant | UBE4B | GRCh38.p7 | 1:10177902 | TCAAAGAACCTGGGC[C/T]TAGGAGGGTTCAGAT | 10277 |
rs12735809 | snp | A/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10084529 | TTTGTCTGGTCTTCC[A/T]AACTAGATTGAAAGC | 10277 |
rs12739977 | snp | A/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10084533 | TCTGGTCTTCCAAAC[A/T]AGATTGAAAGCTCTG | 10277 |
rs12746318 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10137922 | ATCACTTACTAATTC[C/T]ttttttttttttttt | 10277 |
rs12746438 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | UBE4B | GRCh38.p7 | 1:10153676 | agtaAAAggccgggc[A/G]tggtggctcacgcct | 10277 |
rs12747055 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153339 | ggcgagaccccatct[C/T]tacgaaaaatttaaa | 10277 |
rs12747372 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10153489 | agcaagaccctgttt[C/T]taaaaaaaaaaaaaa | 10277 |
rs12751799 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073921 | atttctttctttcta[A/T]ttttttttttttttt | 10277 |
rs12752311 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139213 | ctagcctggccaaca[A/T]agtgaaaacccgtct | 10277 |
rs12752591 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111745 | gcggatcacttgagg[C/T]caggagttcaagaca | 10277 |
rs12759922 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180659 | TAAGATTTTTTTATT[C/T]TAAACAAAATAAAGA | 10277 |
rs13373975 | snp | A/T | 0.0644693 | 0.167566 | intron-variant | UBE4B | GRCh38.p7 | 1:10078075 | aatgcagtggcacga[A/T]cttggctcactgcaa | 10277 |
rs17034490 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | UBE4B | GRCh38.p7 | 1:10050887 | CCAATTCTAGTATTG[C/T]AATAGTTTATTTGTT | 10277 |
rs17034493 | snp | C/T | 0.102726 | 0.202016 | intron-variant | UBE4B | GRCh38.p7 | 1:10074168 | GGAACCTCCATCAGC[C/T]TCAGTCATCACATCC | 10277 |
rs17034495 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | UBE4B | GRCh38.p7 | 1:10075594 | CCGGGTACCTCTATG[C/T]TAAGTAGTCCTGATT | 10277 |
rs17034499 | snp | A/G | 0.0198468 | 0.0976192 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130715 | TCCTTCTCTTTCCAG[A/G]TTAAAGTGGTTGAAA | 10277 |
rs17034501 | snp | C/T | 0.208169 | 0.246476 | intron-variant | UBE4B | GRCh38.p7 | 1:10132968 | TAGGCAGGGCGCCAT[C/T]GGGTTAGGTTTACGT | 10277 |
rs17034540 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE4B | GRCh38.p7 | 1:10161380 | CATTTGTGGGTCTGA[C/T]GATATGCGATCTGAC | 10277 |
rs17034544 | snp | A/C | 0.0681886 | 0.171594 | intron-variant | UBE4B | GRCh38.p7 | 1:10162947 | AGGTTTGTCTTCGCC[A/C]ATCAGCATAGCTGAA | 10277 |
rs17034545 | snp | C/T | 0.237303 | 0.249677 | intron-variant | UBE4B | GRCh38.p7 | 1:10164635 | TTTTTCCTGTGTTAA[C/T]GGATGAAAAAGGCCC | 10277 |
rs17034549 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10165371 | TCAGCACCTCCAGAC[C/G]GTTGGCATCTCTTAC | 10277 |
rs17034554 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10165429 | GGTCTTCAACCTCCA[C/T]TCTTGAGCATGTCCA | 10277 |
rs17034558 | snp | A/G | 0.21303 | 0.247251 | intron-variant | UBE4B | GRCh38.p7 | 1:10168470 | GAGCAGATGTCTGAT[A/G]TCACCACATAGTCTA | 10277 |
rs17034560 | snp | A/G | 0.33875 | 0.233717 | intron-variant | UBE4B | GRCh38.p7 | 1:10169100 | GTTTGTTCTCAACTA[A/G]TAAGACCTGGTTCCT | 10277 |
rs17034563 | snp | G/T | 0.216649 | 0.247765 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170448 | TTTTATGGCCAGTGT[G/T]TAATGCTCTCTAAGC | 10277 |
rs17034569 | snp | C/T | 0.137527 | 0.223271 | intron-variant | UBE4B | GRCh38.p7 | 1:10172142 | TCCCTCTCCTTTATT[C/T]CGTGGGTCTCCTGTG | 10277 |
rs17034584 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE4B | GRCh38.p7 | 1:10179653 | TGAAGCAGAAGGGAA[A/G]TTTATCAAATGCAGA | 10277 |
rs28422033 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164719 | CACTTTCTACCTCCC[A/C]CTGCCCTGGCTGTTC | 10277 |
rs28671063 | snp | A/G | 0.160938 | 0.233598 | intron-variant | UBE4B | GRCh38.p7 | 1:10097873 | TTTCCTCAAGCATTT[A/G]TCCTTATTTTTTTTG | 10277 |
rs28700998 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062101 | TTTTAGTAGAGACGG[G/T]GTTTCACCATGTTGG | 10277 |
rs28812302 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153116 | TTCAGTTTTCCAGTT[A/C/T]TCCTGCAGCACCCCC | 10277 |
rs33967541 | in-del | -/A/AA/AAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135735 | GTGAGACTCTGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 10277 |
rs33997625 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102428 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGCCTCAC | 10277 |
rs34020345 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052025 | ATATTGCTTCTTTGT[C/T]CCCTGTCAGTGCTTG | 10277 |
rs34028637 | in-del | -/T | 0.120674 | 0.21395 | intron-variant | UBE4B | GRCh38.p7 | 1:10034991 | TTTATTTTATGTGGG[-/T]TTTTTTTTTGTTTGT | 10277 |
rs34051219 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164142 | GGCCAGGAGTTTGAG[-/A]CCAGCCTGGCCAACA | 10277 |
rs34066776 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101499 | CTGTTGGTCTTTTGC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs34067760 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10150886 | AAAAAATAGGCTGGG[-/C]CGCAGTGGCTCATGC | 10277 |
rs34094187 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060178 | CATCACTTAATGACA[-/G]GGGATACGTTCTGAG | 10277 |
rs34126347 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076609 | AGTCCTTCATCCAGG[-/T]AGTGCTTGGCAGCAG | 10277 |
rs34152930 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058523 | GAGGCATGGGGTGCT[-/G]GGGTGGTGGGCCAGG | 10277 |
rs34197778 | in-del | -/A | 0.497586 | 0.0346604 | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181078 | AATTTCCTTTGGGGT[-/A]AAAAAAAAAAAAGGA | 10277 |
rs34204373 | in-del | -/T/TT | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10039596 | TTTTTTTTTTTTTTT[-/T/TT]GTATTTTTAGTAAAG | 10277 |
rs34214793 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065393 | AAGCAACCACCAGTG[-/C]CCCAGCTGTGTGTTG | 10277 |
rs34216769 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141493 | GCTGACCCCTTTTAG[-/T]ACTTCCAGAACTCTA | 10277 |
rs34219152 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBE4B | GRCh38.p7 | 1:10111232 | CACACACACACCACG[C/T]GCTACACACACACCC | 10277 |
rs34222398 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078880 | GAGTACAGTGGTGCG[-/C]ACCATAGCTCATTGC | 10277 |
rs34277013 | snp | A/C | 0.233235 | 0.249437 | intron-variant | UBE4B | GRCh38.p7 | 1:10166974 | ACACACACACACAAA[A/C]AAAAAAAATTAGCTG | 10277 |
rs34390177 | in-del | -/A | 0.335788 | 0.23482 | intron-variant | UBE4B | GRCh38.p7 | 1:10049579 | TAAGACCTTTTCTCT[-/A]AAAAAAAAAAAAAAT | 10277 |
rs34394962 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10047988 | TCCTGAGTAACTGGG[-/A]AGGTGTGTGCCACTG | 10277 |
rs34402766 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036041 | AGCCACCGCGCCCGG[-/C]CCGAGGTAGTTTTTT | 10277 |
rs34406285 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056498 | TGAATAAACTAGACC[-/A]AAATCCCTGCTCTCT | 10277 |
rs34413524 | snp | A/C | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10102527 | GCGATTCTCCTGCCT[A/C]AGCCTCCCAAGTAGC | 10277 |
rs34461122 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153486 | CAAAGCAAGACCCTG[-/T]TTCTAAAAAAAAAAA | 10277 |
rs34468946 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158881 | GGGTGTGGTGGCGCA[-/C]CGTCTGTTATCCTAG | 10277 |
rs34527607 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123427 | GAGCAAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 10277 |
rs34575664 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175380 | AAATAGCCGGGTGCA[-/G]GTGGCTCACGCCTGT | 10277 |
rs34580335 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085956 | ACCACGCCCAGCTAA[-/T]TTTTTTTTATTTTTT | 10277 |
rs34591813 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077849 | CCTATGGAACCAAGT[-/A]CCACAGGTCATTGCT | 10277 |
rs34601757 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077657 | ATTTGAGTTCTTTTG[-/A]AAAAACAGCTGGCTG | 10277 |
rs34609417 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110280 | ATAAGGATTAATTTT[-/A]AAAAGGTAAAACATT | 10277 |
rs34652791 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072436 | CATCTTTTTTTTTTT[-/T]CAAACAGGTTTAGGT | 10277 |
rs34690326 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161071 | GTGGAGGTGCTTGTT[-/C]CCCTGGGATTTGCTG | 10277 |
rs34711710 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121869 | GATGTCAAGTTTGAC[-/T]TTTTGACTGGGCAGT | 10277 |
rs34727560 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135442 | AACCCCGTCTCTACT[-/A]AAAATACAAAAATTA | 10277 |
rs34800705 | in-del | -/G | 0.0310518 | 0.120672 | intron-variant | UBE4B | GRCh38.p7 | 1:10157379 | TACTTGGGATGCTGA[-/G]GGTGGGAGGATCACT | 10277 |
rs34801526 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131215 | GTGTGATGGCTCATG[-/C]CCTGTAATCCCAACA | 10277 |
rs34811287 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114065 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGA | 10277 |
rs34832564 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146308 | ATACAAAAATTAACT[-/G]GGGTGTGGTGGCACA | 10277 |
rs34846271 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148039 | GAGACCATCTTTGCT[-/A]ACACGGTGAAACCCC | 10277 |
rs35021874 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102001 | TGTGTGTGTGTGTGT[-/GT]ATTAATATAGATAAT | 10277 |
rs35084228 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131572 | AAAGCCTATTTTATT[-/A]AAAACTGTAACTGCC | 10277 |
rs35168475 | in-del | -/A | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032692 | TTCCCCGACGCGAGT[-/A]CTGGGAGTCGTCCCT | 10277 |
rs35190028 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148078 | TAAAAATACAAAAAA[-/T]TAGCTGGGCGCTGTG | 10277 |
rs35217181 | in-del | -/GGT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059088 | GCAAAAAGTTAGCCA[-/GGT]GTGGCGGTGGGCGCC | 10277 |
rs35252601 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | UBE4B | GRCh38.p7 | 1:10174650 | GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCATTG | 10277 |
rs35270223 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169551 | AAAGTGCAAGGCCAT[-/G]GGAGCATGAAACAAA | 10277 |
rs35280382 | snp | A/C | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10097072 | ATAATAATAATAATA[A/C]CCAAATAGAATATCT | 10277 |
rs35314296 | in-del | -/T | | | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181563 | CTGTAATCCCAGCAC[-/T]TTTGGGAGGCTGAGG | 10277 |
rs35316894 | snp | C/T | 0.463881 | 0.12944 | intron-variant | UBE4B | GRCh38.p7 | 1:10143930 | CTTCACAGTACTCAC[C/T]CTGCCTTCAGTGAGG | 10277 |
rs35325221 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122774 | CCCTGATGAAAGGGC[-/T]TTTTATCAAATTTTC | 10277 |
rs35395193 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049502 | CAATCCCTGCTACTT[-/T]GGGAGGCCAAGGCAG | 10277 |
rs35399830 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070808 | TTTATTGAATCAAGT[-/A]AAAAAAGAAAATCTG | 10277 |
rs35403209 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10145560 | AGCCAAGATGGCGCC[A/C]CTGCACTCCAGCCTG | 10277 |
rs35406080 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133093 | AAGGGGGCAGCCAGG[-/C]AACAGACCCAAGAAG | 10277 |
rs35451816 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097568 | TAATCCCATCACTTT[-/G]GGGAGGCCGACGCAG | 10277 |
rs35470872 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082571 | AAAGAGAGCAGTATG[-/T]TTGGCATAAGTACCA | 10277 |
rs35481368 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117745 | AATACTAGGAACTTA[-/G]GGATGTGTCGATGAA | 10277 |
rs35493669 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148084 | TACAAAAAATTAGCT[-/G]GGCGCTGTGGCGGGT | 10277 |
rs35513799 | in-del | -/T | 0.0755793 | 0.179102 | intron-variant | UBE4B | GRCh38.p7 | 1:10043422 | AAATTGAGATGCTGC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs35520483 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161839 | CAGCCACTGAGATAC[-/T]TTCCTTGGTCGCTTA | 10277 |
rs35569014 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136483 | GAGTAAGACCCTCTT[-/A]AAAAAAAAAAAAAAA | 10277 |
rs35592325 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114067 | GAGACTCCGTCTCAA[A/T]AAAAAAAAAAAGAAA | 10277 |
rs35609175 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10136965 | AAAAGTATCTTTAAA[C/T]TTCATAAAAATTCAA | 10277 |
rs35623949 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10102952 | TCTTCACCAGGAGCC[-/T]TTCCTCGGGCCCTGA | 10277 |
rs35632014 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | UBE4B | GRCh38.p7 | 1:10120980 | AATTATATACATGTA[C/T]CAAAACTTTAAAAAA | 10277 |
rs35646986 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UBE4B | GRCh38.p7 | 1:10062203 | CTGAGCCACCACACC[C/T]GGCCCTATTTTTTCT | 10277 |
rs35655615 | in-del | -/A | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10127202 | GAAATTTTGTTACTT[-/A]AAAAAAAAAAAACCT | 10277 |
rs35745672 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149506 | TGCAGATAATGTATT[-/C]CCTTGAAAATTGAGT | 10277 |
rs35789113 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087404 | AATGTTAATGTCTGG[G/T]TCATTTGTCAAAACT | 10277 |
rs35822677 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118868 | TTGGCCAGGCTGGTC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs35830844 | in-del | -/G | 0.16028 | 0.233346 | intron-variant | UBE4B | GRCh38.p7 | 1:10134204 | AAGAATTATCGTGAT[-/G]GTTCAGTAAAAGAAT | 10277 |
rs35894551 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068950 | ATGTATTCTCCCAAT[-/G]CTTCTCCTACTCCTT | 10277 |
rs35922640 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100029 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 10277 |
rs35941004 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128164 | TATCACCATATTATG[-/T]TAGATGTTCCTTCAT | 10277 |
rs36052900 | in-del | -/T | 0.447938 | 0.152711 | intron-variant | UBE4B | GRCh38.p7 | 1:10074345 | GGCCTTTTTTTTTTT[-/T]AACAGCCTATATAAT | 10277 |
rs36091946 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144487 | ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 10277 |
rs41280786 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10072975 | TCTTGATCTAGAATC[A/G/T]TGTCAATTAAAAGTA | 10277 |
rs41280788 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | UBE4B | GRCh38.p7 | 1:10073031 | TCTCGTTAGGTATCA[A/G]TGTAGACTATAGATA | 10277 |
rs41280790 | snp | A/G | 0.00498601 | 0.0496804 | intron-variant, utr-variant-5-prime | UBE4B | GRCh38.p7 | 1:10101206 | ATAAGGTTGGTAAGC[A/G]ATGAAGCCCTTGGTA | 10277 |
rs41280792 | snp | A/G | 0.0335299 | 0.125063 | intron-variant | UBE4B | GRCh38.p7 | 1:10101242 | AATAGAAATAAACAC[A/G]TTTCATGTCTTGTAT | 10277 |
rs41280794 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10105972 | TTTTAGAAGCAGTTG[A/G]CTGTGTATACTACAT | 10277 |
rs41280796 | snp | C/T | 5.00179e-05 | 0.00500065 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106247 | TCTGGAGCTCTGTTC[C/T]CGTGATGGGCCCGTC | 10277 |
rs41280802 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE4B | GRCh38.p7 | 1:10128421 | AAAATCAGAAATCAT[C/T]GTGATCATTCTCTAG | 10277 |
rs41280804 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10132780 | TGGGTGGCAGGAAAG[A/G]CCTCCCTGAGGAGGT | 10277 |
rs41280806 | snp | A/G | 0.0341751 | 0.126173 | intron-variant | UBE4B | GRCh38.p7 | 1:10151293 | CAGCAGTTTCTCAGC[A/G]GTCTCTTTCTTGCTC | 10277 |
rs41310363 | snp | A/G | 0.0724406 | 0.17599 | intron-variant | UBE4B | GRCh38.p7 | 1:10179589 | TGCAGTTTGAGGTGC[A/G]GCGCTGGCGTCAGTA | 10277 |
rs55678257 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | UBE4B | GRCh38.p7 | 1:10103513 | TCTCAGCTGACTGCA[A/G]CTTCTGCCTCCCGAG | 10277 |
rs55704135 | snp | A/G | 0.138546 | 0.223781 | intron-variant | UBE4B | GRCh38.p7 | 1:10134381 | GCCGGGCGTGGTGGC[A/G]GGTGCCTGTAATCCC | 10277 |
rs55936075 | in-del | -/CACA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111090 | ACACACACACACACA[-/CACA]GTCTTTCCACCATAT | 10277 |
rs56019503 | snp | A/C | 0.0337757 | 0.125487 | intron-variant | UBE4B | GRCh38.p7 | 1:10168100 | AGCTGATGACCAGGA[A/C]CGAGCCTTACTCAGC | 10277 |
rs56167268 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158589 | GACTGTTTGCTTGGT[C/T]TCAGACTCCTTTGAG | 10277 |
rs56682893 | snp | A/G | 0.170733 | 0.237101 | intron-variant | UBE4B | GRCh38.p7 | 1:10055384 | CACTGGCAGCATCAT[A/G]GCTCACTGTAGCCTT | 10277 |
rs56760324 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | UBE4B | GRCh38.p7 | 1:10048126 | GGCCCTGGGATTATA[A/G]GCATGAGCCACTGCA | 10277 |
rs56777705 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111969 | TCAAAAAAAAAAAAA[-/A]GAAAGAAAATGCAAA | 10277 |
rs56948052 | in-del | -/AA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168907 | AAAAAAAAAAAAAAA[-/AA]GAAGAAGAAAAAGCA | 10277 |
rs57015590 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | UBE4B | GRCh38.p7 | 1:10146578 | GGCCAGCATTTTGCC[C/T]GAGGGCAGCTCGTAA | 10277 |
rs57037935 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10062564 | AGGTCTGCCCACCTT[-/G]GGCTCCCAAAGTGTT | 10277 |
rs57054060 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10151216 | AGGGCACTCCCAAAC[C/T]TACTTATCCTGCCTT | 10277 |
rs57215910 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088011 | TTTTACAGGAATTAT[C/T]CCAGCTTTGACCATG | 10277 |
rs57216908 | snp | C/T | 0.1652 | 0.235179 | intron-variant | UBE4B | GRCh38.p7 | 1:10063980 | TTCAAAAGATGTCTT[C/T]CTTGCCTTCACGAAC | 10277 |
rs57314761 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | UBE4B | GRCh38.p7 | 1:10124265 | CTTCTGGGTTCGAGC[A/G]ATTCTCCTGCCTCAG | 10277 |
rs57324977 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE4B | GRCh38.p7 | 1:10154009 | ATCACTTGAACCCGC[A/G]AGGCAGAGGTTACGG | 10277 |
rs57325800 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | UBE4B | GRCh38.p7 | 1:10154847 | ATCTCCATCTCAAAA[A/G]AAAAAAAAAGGAATG | 10277 |
rs57486350 | in-del | -/GTGTGTGT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090832 | TGTGTGTGTGTGTGT[-/GTGTGTGT]AATACTGGAACAGGC | 10277 |
rs57598154 | in-del | -/GTGT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090829 | TGTGTGTGTGTGTGT[-/GTGT]AATACTGGAACAGGC | 10277 |
rs57761656 | snp | A/G/T | 0.0444908 | 0.142359 | intron-variant | UBE4B | GRCh38.p7 | 1:10161423 | TCCTTCCATGAAATC[A/G/T]TATTGCAGGATTGGA | 10277 |
rs57769250 | in-del | -/A/AA | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10144749 | AAAAAAAAAAAAAAA[-/A/AA]GAAAGAAAGAAAGAA | 10277 |
rs57841357 | snp | A/C | 0.0640965 | 0.167152 | intron-variant | UBE4B | GRCh38.p7 | 1:10054890 | TCCCGGGTTCAAGCG[A/C]TTCTCCTGCCTCAGC | 10277 |
rs57848761 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065227 | AAGTATGGAGAACCA[C/T]TAAAGCAGATGGGAA | 10277 |
rs57860112 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034489 | TTGTAAAAAAAAAAA[-/A]CAACCAAAAAGCAGT | 10277 |
rs58064995 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10051907 | CTTTGGCATCTTGTC[C/T]AGTTCTTTGGCAGCA | 10277 |
rs58109538 | in-del | -/T | 0.351418 | 0.228505 | intron-variant | UBE4B | GRCh38.p7 | 1:10103608 | TTTGTAGTTTTTTTT[-/T]GTTTGTTTTGTTTTT | 10277 |
rs58272276 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049593 | TAAAAAAAAAAAAAA[-/A]TTTTTTTAAATTAGG | 10277 |
rs58277158 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | UBE4B | GRCh38.p7 | 1:10115990 | ATGTTGTTATGTGGC[A/G]CATGTGTTACAAATG | 10277 |
rs58320071 | in-del | -/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031108 | GAGTCTTTTTTTTTT[-/T]GTGACGGAGTCTCGC | 10277 |
rs58453167 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | UBE4B | GRCh38.p7 | 1:10062943 | CCTGGGAAACAAGAG[C/T]GAAACTCCGTCTCAA | 10277 |
rs58558244 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE4B | GRCh38.p7 | 1:10077820 | TTTCAAATGTACATG[A/G]TAACATAACTAGTGC | 10277 |
rs58753213 | in-del | -/A/C | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10135751 | AAAAAAAAAAAAAAA[-/A/C]CAGATACAAATTGAA | 10277 |
rs58810363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086065 | CAAGCTCCACCTCCC[G/T]GGTTCACGCCATTCT | 10277 |
rs58810882 | snp | A/T | 0.0923359 | 0.194016 | intron-variant | UBE4B | GRCh38.p7 | 1:10097049 | GCATCAAAAAAAAAA[A/T]AAAAATAATAATAAT | 10277 |
rs58900002 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | UBE4B | GRCh38.p7 | 1:10076803 | CCAGGCTGGAGTGCA[A/G]TGGCATGATCTCGAC | 10277 |
rs58953060 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093761 | GGGCAGTGGGGCGAT[C/T]TTGGCTCACTGCAAC | 10277 |
rs59570346 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | UBE4B | GRCh38.p7 | 1:10102385 | ACTTTTGATAATGAC[C/T]TTGCTCTTTTTTTTT | 10277 |
rs59727687 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10151188 | AAAAGTCACTGTAAA[C/G]TGAATGAGTTCAAGG | 10277 |
rs59740055 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039091 | AAAAACACACACACA[A/G]AAAAACAAACAAAAA | 10277 |
rs59843720 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | UBE4B | GRCh38.p7 | 1:10055410 | GCCTTGAACTCCTGG[A/G]CTCCGGTGATCCTCC | 10277 |
rs59870161 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10062850 | AATCCCAGCGACTCG[A/G]GAGGCTGAGGCAGGA | 10277 |
rs60067828 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131963 | TCTCAAAAAAAAAAA[-/A]CAACAAAAATGCAAA | 10277 |
rs60085278 | snp | G/T | 0.174288 | 0.23826 | intron-variant | UBE4B | GRCh38.p7 | 1:10103638 | TTTGTTTTTGTTTTT[G/T]TTTTTTTTTTTGAGA | 10277 |
rs60208411 | snp | C/T | 0.348354 | 0.22984 | intron-variant | UBE4B | GRCh38.p7 | 1:10086322 | CATGTTGGTCAGGCT[C/T]GTGTTGAACTCCTGA | 10277 |
rs60259277 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070289 | CAGAAAAAAAAAAAA[-/A]TTACATGCTACACAG | 10277 |
rs60413811 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | UBE4B | GRCh38.p7 | 1:10124226 | GAGTGCAGTGGCGCC[A/G]TCTCAGCTCACTGCA | 10277 |
rs60495933 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | UBE4B | GRCh38.p7 | 1:10081970 | TCTTCCCACCTTGGC[C/T]TCCCAATGTGTTGGG | 10277 |
rs60565991 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10045955 | GATAGATGTTTATTT[C/T]TCTCTAAATAGAAGT | 10277 |
rs60837845 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10147228 | AGGCGCAGTGGTTCA[C/T]GCCTGTAATCCCAGC | 10277 |
rs60838123 | in-del | -/ATA | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10152296 | ATAATAATAATAATA[-/ATA]CCACTTTTCACCTGT | 10277 |
rs60854765 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034047 | GTGTCTTCAGGAATT[-/T]AAAGAACAATTTTGG | 10277 |
rs60975850 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107577 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs61048581 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | UBE4B | GRCh38.p7 | 1:10087369 | CAGGATTCCTGTGTA[C/T]CCTTCATCCAGTCTC | 10277 |
rs61393825 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162624 | TTTTTTTTTTTTTTT[-/T]CTTTTTTAATTTCAA | 10277 |
rs61445642 | in-del | -/T | 0.451732 | 0.147663 | intron-variant | UBE4B | GRCh38.p7 | 1:10041302 | CCTCTAAAACAAGAC[-/T]TAACCTCAGCCAACT | 10277 |
rs61462323 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | UBE4B | GRCh38.p7 | 1:10062620 | CCGGCCGCCTTAATG[C/T]ATTTTTTGTTAATCA | 10277 |
rs61563451 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076763 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCGC | 10277 |
rs61644342 | in-del | -/TTT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118899 | TTTTTTTTTTTTTTT[-/TTT]GAGATGGAGTCTCAC | 10277 |
rs61650275 | snp | C/G | 0.465473 | 0.126772 | intron-variant | UBE4B | GRCh38.p7 | 1:10062721 | CAGCATTTTGGGTGA[C/G]TGAGGCAAGTGGATC | 10277 |
rs61760196 | snp | C/G | 0.0690032 | 0.172453 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130517 | TGCTTCTTTGCGGTT[C/G]TGGTTGCCGAAATCC | 10277 |
rs61782893 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032349 | AAAAAAAAAAAAACC[A/C]AGGAAGTATCTCTAA | 10277 |
rs61782894 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038451 | CTGTTTCTCATTAGA[G/T]AAAACATTATAATCA | 10277 |
rs61782895 | snp | A/C | 0.100231 | 0.200173 | intron-variant | UBE4B | GRCh38.p7 | 1:10052095 | TTTTTGAGACGGGGT[A/C]TTGCTCTGTCACCCA | 10277 |
rs61782898 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | UBE4B | GRCh38.p7 | 1:10071810 | AGCTGAGACTATAGG[A/C]AGGCACCGCTGAACC | 10277 |
rs61782899 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBE4B | GRCh38.p7 | 1:10085852 | TGGAGTACAGTGGCG[C/T]GATTTTGCCTCACTG | 10277 |
rs61782900 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10086926 | AACTCCTGATCTCGG[C/T]CTCCCAAAGTGCTGG | 10277 |
rs61782901 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10088421 | AGTCTCACTCTGTTG[C/T]CCAGGCTGGCGTGCA | 10277 |
rs61782902 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | UBE4B | GRCh38.p7 | 1:10093178 | GAAATTTTAAAGCCT[A/G]CTTATTTACTACCAT | 10277 |
rs61782903 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10098017 | CTGGGATTACAGACA[G/T]GGGCCACCACGCATG | 10277 |
rs61782904 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBE4B | GRCh38.p7 | 1:10098028 | GACATGGGCCACCAC[A/G]CATGGCTAATTTTTG | 10277 |
rs61782905 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10118043 | GGCATTCTTTTTTCA[A/G]CGTATGACTAAGCAA | 10277 |
rs61782918 | snp | C/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10127763 | CTGGTGATACAGAAG[C/G]TAGGAAGACAAGGTC | 10277 |
rs61782919 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10133653 | TGGTGGCTCACGCCT[A/G]TAATCTCAGCACTTT | 10277 |
rs61782920 | snp | A/G | 0.213635 | 0.247341 | intron-variant | UBE4B | GRCh38.p7 | 1:10135338 | AGGCCTGGCGTGGTG[A/G]CTCATACCTATAATC | 10277 |
rs61782922 | snp | A/T | 0.160609 | 0.233472 | intron-variant | UBE4B | GRCh38.p7 | 1:10140946 | TCAAAGTTTGGGTCA[A/T]CTAGTTGGTTGCATA | 10277 |
rs61782923 | snp | A/G | 0.160609 | 0.233472 | intron-variant | UBE4B | GRCh38.p7 | 1:10141464 | CCCCTAGAGCCTCCA[A/G]AAGGAACCATCCCTG | 10277 |
rs61782924 | snp | C/G | 0.462909 | 0.131034 | intron-variant | UBE4B | GRCh38.p7 | 1:10142698 | AAGGTTGCATTCCCT[C/G]CAGAGGCTCTAGGGG | 10277 |
rs61782925 | snp | A/G | 0.179425 | 0.239831 | intron-variant | UBE4B | GRCh38.p7 | 1:10146407 | CAGTGAGCCAAGATC[A/G]CGCCACTGCACTTCA | 10277 |
rs61782926 | snp | A/G | 0.237593 | 0.249692 | intron-variant | UBE4B | GRCh38.p7 | 1:10149913 | TAGTCCCAGACATGC[A/G]GGAGGATTGCTTGAG | 10277 |
rs61782927 | snp | A/G | 0.268995 | 0.249277 | intron-variant | UBE4B | GRCh38.p7 | 1:10154031 | AGGTTACGGTGAGCC[A/G]AGATCGCGCCATTGT | 10277 |
rs61782928 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155086 | GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG | 10277 |
rs61782929 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155088 | GAGAGAGAGAGAGTG[A/T]GTGTGTGTGTGTGTG | 10277 |
rs61782930 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155090 | GAGAGAGAGAGTGTG[A/T]GTGTGTGTGTGTGTG | 10277 |
rs61782931 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155092 | GAGAGAGAGTGTGTG[A/T]GTGTGTGTGTGTGTG | 10277 |
rs61782932 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155094 | GAGAGAGTGTGTGTG[A/T]GTGTGTGTGTGTGTG | 10277 |
rs61782933 | snp | A/G | 0.192088 | 0.2432 | intron-variant | UBE4B | GRCh38.p7 | 1:10156333 | CACTCTTGACCTCCC[A/G]GGCTCAAGTGATCCT | 10277 |
rs61782934 | snp | A/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10157033 | GAAAAAAAAAATTTT[A/T]GAGACAGAGTCTTGC | 10277 |
rs61782935 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10161712 | GTGTTTTTTCCCTTT[C/T]AGTTGATCTTGGGTT | 10277 |
rs61782936 | snp | C/G | 0.194278 | 0.243711 | intron-variant | UBE4B | GRCh38.p7 | 1:10162265 | TGCAATCTTTGCCTC[C/G]TGGGTACAAGTGATT | 10277 |
rs61782937 | snp | C/T | 0.393619 | 0.204631 | intron-variant | UBE4B | GRCh38.p7 | 1:10163560 | GTAGTCCCAGCTACT[C/T]GAGAGGCTGAGGCAG | 10277 |
rs61782938 | snp | A/G | 0.257454 | 0.249889 | intron-variant | UBE4B | GRCh38.p7 | 1:10165540 | GAGCCAAATCCTGTG[A/G]TGAGAGCAGCCTACA | 10277 |
rs61782939 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | UBE4B | GRCh38.p7 | 1:10174267 | GGCACAGTGGAAGGC[A/G]GCTGTAATTCCAGCT | 10277 |
rs67066058 | in-del | A/CAC | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10166972 | ACACACACACACACA[A/CAC]AAAAAAAATTAGCTG | 10277 |
rs70998345 | in-del | -/A | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10070460 | AAAAAAAAAAAAAAA[-/A]CCATTACCAGATCCC | 10277 |
rs70998346 | in-del | -/GAAAA | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10092539 | ACCCATTTCTTAAAA[-/GAAAA]TAAGGAGGCCAGGCA | 10277 |
rs70998350 | in-del | -/A | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10127214 | CTTAAAAAAAAAAAA[-/A]CCTATTAAAAATGCA | 10277 |
rs70998351 | in-del | -/TT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137922 | ATCACTTACTAATTC[-/TT]TTTTTTTTTTTTTTT | 10277 |
rs70998352 | in-del | -/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10157381 | CTTGGGATGCTGAGG[-/G]TGGGAGGATCACTTG | 10277 |
rs71299826 | in-del | -/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10118901 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 10277 |
rs71583833 | in-del | -/C | 0.5 | 0 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031375 | AGCCACTGCGCCCAG[-/C]CCGGGAGTGACTGTT | 10277 |
rs71583834 | in-del | -/A | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10035381 | TTTCTCTTAAGGCAG[-/A]AGATACTGTTTTTTT | 10277 |
rs71583835 | in-del | -/C | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10055888 | GCATCACTGCATTCC[-/C]AGCCTGGATGACAGA | 10277 |
rs71583836 | in-del | -/TATGTATGTAT/TTATGTATGTAT | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10071707 | TATTTATGTATGTAT[-/TATGTATGTAT/TTATGTATGTAT]GAATTAGAGGTGGGT | 10277 |
rs71583837 | in-del | -/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10073944 | TTTTTTTTTTTTTTT[-/T]GGAGATGAGGTCTCA | 10277 |
rs71583838 | in-del | -/C | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10082801 | CCTAATGCTCTCCCT[-/C]CCCCTTGACCCCACC | 10277 |
rs71583839 | in-del | -/GT/TG | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10090794 | GAAGCCTATGCATTT[-/GT/TG]GTGTGTGTGTGTGTG | 10277 |
rs71583840 | in-del | -/A | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10123191 | TCTCAACACTTTGGG[-/A]AGGCTGAGGCGGATG | 10277 |
rs71583841 | in-del | -/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10124040 | TCAGCCGCCCAAAGT[-/G]CTGGGATTACAGGCA | 10277 |
rs71583842 | in-del | -/ATAGATAG | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10126303 | AGACTCCGTCTCAAT[-/ATAGATAG]ATAGATAGATAGATA | 10277 |
rs71583843 | in-del | -/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10129694 | TCTGTCACCCAGGCT[-/G]GGATGGAGTGCAGTG | 10277 |
rs71583844 | in-del | -/C | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10140014 | GTGTGAGCCACTGCA[-/C]CCGGCCCATTTTAAT | 10277 |
rs71643082 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10179108 | GAATTCCCAGAAGTC[C/T]TAAGACAAAGAATTC | 10277 |
rs72638953 | snp | A/T | 0.124491 | 0.216211 | intron-variant | UBE4B | GRCh38.p7 | 1:10065935 | TTCAATTCAATTTTT[A/T]AAAAAATGGAAAATA | 10277 |
rs72638956 | snp | A/C | 0.0490535 | 0.14873 | intron-variant | UBE4B | GRCh38.p7 | 1:10103403 | CATTACCTCCTCTTT[A/C]TTTATTTATTTATTT | 10277 |
rs72638958 | snp | A/G | 1.64852e-05 | 0.00287094 | intron-variant | UBE4B | GRCh38.p7 | 1:10129474 | ACCTGATGGGCTTGC[A/G]CATTTTCAGTGAATA | 10277 |
rs72859578 | snp | C/G | 0.130008 | 0.219321 | utr-variant-5-prime, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10033012 | TACTTGGTGGGGCGA[C/G]GGGGAAAGAGTAGGG | 10277 |
rs72859583 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | UBE4B | GRCh38.p7 | 1:10048893 | TGTGGTGAGCTTATC[G/T]TTTTCTGTTTTAACT | 10277 |
rs72859586 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | UBE4B | GRCh38.p7 | 1:10050077 | CTTGCTGATCTGAAA[A/G]GCTGGTTTTTTTTGA | 10277 |
rs72859587 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10051424 | TGGTGTCCATATAAC[A/T]TCTAACAAATCTTTT | 10277 |
rs72859590 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | UBE4B | GRCh38.p7 | 1:10057243 | AGAATGGGGTTAGGC[A/G]TGTTTAACGTTCTTC | 10277 |
rs72859593 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10059495 | CTTGGGAGGCTCTCC[C/T]GGAAGGGGCCATCAT | 10277 |
rs72859595 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10059721 | CCCATTCCTCTATGC[C/G]TCTCACCTCCACGTG | 10277 |
rs72859599 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | UBE4B | GRCh38.p7 | 1:10059950 | GTGCTTTGTTTACTT[A/G]TTTACTAAGACCCTG | 10277 |
rs72859602 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10063397 | CCTTCTGTATTTTCA[A/G]TTTTAGGGTATTTTA | 10277 |
rs72861408 | snp | C/T | 0.108755 | 0.206276 | intron-variant | UBE4B | GRCh38.p7 | 1:10064174 | CTCCTTTGTTCCTCG[C/T]CTGCCTAACCCCTAC | 10277 |
rs72861412 | snp | A/G | 0.046775 | 0.145601 | intron-variant | UBE4B | GRCh38.p7 | 1:10065578 | CTGGGCCAGTGTGGA[A/G]TTTGCTCTGCCTCTT | 10277 |
rs72861417 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | UBE4B | GRCh38.p7 | 1:10071679 | AACATACAGTATATA[C/T]GTATTTATGTATGTA | 10277 |
rs72861420 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10074696 | ATTCTCCTGGTTTTC[A/G]TGCATTCTCTGTATC | 10277 |
rs72861422 | snp | A/G | 0.103082 | 0.202275 | intron-variant | UBE4B | GRCh38.p7 | 1:10078427 | AAGAGCTTTTAGCCT[A/G]GTTGGGGAGGAAATG | 10277 |
rs72861424 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10080885 | CAAATAGACAGTAGA[C/T]GGTGGTTACCAGAGG | 10277 |
rs72861427 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10082449 | GAGGTAGCAGTGAGC[C/T]GAAATTGTGCCATGC | 10277 |
rs72861431 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | UBE4B | GRCh38.p7 | 1:10087586 | TTTGTCTGGTGTTTT[C/G]CTCATGATAAGACTG | 10277 |
rs72861436 | snp | C/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094203 | TCTGTCCCTGTACTA[C/G]TGACTACAGTTTCAC | 10277 |
rs72861437 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094755 | ACATTTTATTATACT[C/T]GCTTTATCACATATT | 10277 |
rs72861447 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | UBE4B | GRCh38.p7 | 1:10102893 | GTATTCCTATTGAAA[C/T]ACCTAACTCATACCT | 10277 |
rs72861448 | snp | C/T | 0.00443626 | 0.0468876 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106380 | ATCCCCGCGGTATCG[C/T]CCCTACACTGTCACT | 10277 |
rs72861450 | snp | C/G | 0.108926 | 0.211758 | intron-variant | UBE4B | GRCh38.p7 | 1:10107170 | CAAAAGCTTCTCCCC[C/G]TCTTGTTTTTTCTTT | 10277 |
rs72861452 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10110817 | TCACTGCTTGGGGTT[A/G]AAACATAGAAACAGT | 10277 |
rs72861453 | snp | C/T | 0.163236 | 0.234461 | intron-variant | UBE4B | GRCh38.p7 | 1:10111260 | CCCCCACACCAAGCA[C/T]ACATGCACATACGTG | 10277 |
rs72861456 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10114982 | GTTACCTACTCAGTC[A/G]GCAGGGAGTTGGCTG | 10277 |
rs72861457 | snp | A/G | 0.105924 | 0.204309 | intron-variant | UBE4B | GRCh38.p7 | 1:10118288 | TCTTTGGGCTTTGTT[A/G]TACTTAGCCTTAGTG | 10277 |
rs72861490 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10128645 | GCAGTGAGAACGCTT[C/T]CTTCTGAGTTGAGGC | 10277 |
rs72861491 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10129161 | AGGGTAAAGCTTGAG[G/T]AATTTTTAGTTTCAT | 10277 |
rs72861493 | snp | C/G | 0.0836354 | 0.186609 | intron-variant | UBE4B | GRCh38.p7 | 1:10130066 | TTCATCCAATAGTAT[C/G]CTGAAACTTAAACAT | 10277 |
rs72861501 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE4B | GRCh38.p7 | 1:10132891 | GTACAAGCCCAGCAC[A/G]CAGGCTTTTGTGGCT | 10277 |
rs72864109 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10144809 | GCTGGTTGTAAGATA[C/T]ACTCTGATTTTAAAG | 10277 |
rs72864112 | snp | C/T | 0.030665 | 0.119967 | intron-variant | UBE4B | GRCh38.p7 | 1:10152863 | TAGCCATCTTCTATC[C/T]CTCAGTCTGGGGACC | 10277 |
rs72864116 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | UBE4B | GRCh38.p7 | 1:10154747 | CTCTGGAGTCTAAGG[C/T]AGATGAATCACTTGA | 10277 |
rs72864119 | snp | C/T | 0.030665 | 0.119967 | intron-variant | UBE4B | GRCh38.p7 | 1:10159897 | CTCTTATGGTCAGAA[C/T]TGTGTTCCAGCTAAA | 10277 |
rs72864120 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE4B | GRCh38.p7 | 1:10163241 | TGGCTAATTAAAAAA[A/G]TTTTTTTTATAGAGA | 10277 |
rs72864129 | snp | A/G | 0.137867 | 0.223442 | intron-variant | UBE4B | GRCh38.p7 | 1:10172376 | AAAATCCTTTGAGGT[A/G]GGTTCTGTAAAGTCT | 10277 |
rs72864132 | snp | C/T | 0.137867 | 0.223442 | intron-variant | UBE4B | GRCh38.p7 | 1:10172526 | CAGTCTCTCTGCTGT[C/T]CACTTAAAATGCCCA | 10277 |
rs72864146 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE4B | GRCh38.p7 | 1:10177992 | GGGTCCACGGTGGGC[A/G]CCTGACCTCCACTCC | 10277 |
rs74051806 | snp | A/G | 0.029116 | 0.117091 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032433 | AACTGGGCTTTCCTG[A/G]AGGAGGTGGAAGAGT | 10277 |
rs74051807 | snp | C/T | 0.189261 | 0.242509 | intron-variant | UBE4B | GRCh38.p7 | 1:10058720 | CAGCGGCTGGTGTGA[C/T]ACTGACCTGAGCCTT | 10277 |
rs74051808 | snp | C/T | 0.279726 | 0.248226 | intron-variant | UBE4B | GRCh38.p7 | 1:10089471 | ATCTTGCCACTGTAC[C/T]GCAGCCCAGGTATCA | 10277 |
rs74224895 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBE4B | GRCh38.p7 | 1:10108249 | GTCTGGGCAATCCAT[C/T]GAAGAACATATGAGG | 10277 |
rs74340264 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10128796 | TTGATTGAGTTACCA[C/T]GGGCATGCTAAATTA | 10277 |
rs74352466 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | UBE4B | GRCh38.p7 | 1:10059657 | GGGCAAGGCCGAGGC[A/G]TGAAGGGCGGCAGCC | 10277 |
rs74375613 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | UBE4B | GRCh38.p7 | 1:10145176 | CCAATAAAATAGTAT[A/T]TTTTAAAACTTGTTG | 10277 |
rs74426354 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | UBE4B | GRCh38.p7 | 1:10033916 | TTTGCTTCTTTCCGA[C/G]TGTTCTTTTAGGGTA | 10277 |
rs74433442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10076706 | TGTAGGGGGTCCTTC[C/T]ACTTCCAGTTGCTTC | 10277 |
rs74474963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10127698 | TATTCCACTGATTGG[A/G]TTCCATTATACCATG | 10277 |
rs74485639 | snp | C/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10098403 | GTATCTTTAAACTCA[C/G]AGTGTGGCACAGACA | 10277 |
rs74499985 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | UBE4B | GRCh38.p7 | 1:10170136 | CATTTCCTTTGCTAC[A/G]CTATTTACTATCTGG | 10277 |
rs74500145 | snp | A/C/G | 0.00637415 | 0.0561569 | intron-variant | UBE4B | GRCh38.p7 | 1:10111273 | CATACATGCACATAC[A/C/G]TGCCCCATTCTAACT | 10277 |
rs74605718 | snp | A/G | 0.084728 | 0.187577 | intron-variant | UBE4B | GRCh38.p7 | 1:10175380 | AAAATAGCCGGGTGC[A/G]GTGGCTCACGCCTGT | 10277 |
rs74669740 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10059764 | CAGCTGTAGGCATCC[A/G]AAGTTGTTGAGCGTA | 10277 |
rs74676568 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE4B | GRCh38.p7 | 1:10165452 | CATGTCCATATCAGG[A/G]ATGGTGTTAAACATC | 10277 |
rs74719934 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | UBE4B | GRCh38.p7 | 1:10069780 | CCTCAAATGATCCAC[C/T]GCCTCGGACTCCCCT | 10277 |
rs74733539 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBE4B | GRCh38.p7 | 1:10086463 | ACCTTGGATGTAGAG[A/G]TAAATGAGGTATGGG | 10277 |
rs74776834 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | UBE4B | GRCh38.p7 | 1:10149602 | GAATGAACATCCCAA[A/T]ACCAGAAATATCCAC | 10277 |
rs74835018 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070004 | ACTTGGCCCGGCATG[A/G]TGGCTCACACTTGTA | 10277 |
rs74845825 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10178077 | GTTCACCAGGGTGGT[C/G]TAACGTCCATGGAGC | 10277 |
rs74875629 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10041215 | AATTTATTGAAAGGC[A/G]CACAACTAGTAAGTG | 10277 |
rs74911024 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10063910 | TGAAACTGTCTCAAT[A/G]AAAAAAAAAAAAAAG | 10277 |
rs74946358 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10138709 | ATAACCTTGAAATTT[A/C]CATCTTGTTTCAGTT | 10277 |
rs74962667 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10046232 | GAAGGCTGAGAAATA[A/G]TTTTTCTTGGGCAGC | 10277 |
rs75002255 | snp | A/C | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10111956 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAGA | 10277 |
rs75011205 | snp | A/T | 0.0729237 | 0.177671 | intron-variant | UBE4B | GRCh38.p7 | 1:10067158 | CTGCCTGCAATCACA[A/T]TGGCCTTCACTGTTT | 10277 |
rs75035497 | snp | C/G | 0.492727 | 0.0598633 | intron-variant | UBE4B | GRCh38.p7 | 1:10080604 | GCTGAAGAGATACCT[C/G]TACTCATGTTCATTG | 10277 |
rs75051538 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10053758 | CAGTGGCGTGATCAC[A/G]GCTCACTTGCAGCCT | 10277 |
rs75074334 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10133317 | CCGTTTACTAACTGC[A/G]GGACCTTAGACAGTG | 10277 |
rs75103101 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111022 | TGTCTCTCTCTGTCT[C/G]TCTCTGTCTTTCTCT | 10277 |
rs75225462 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBE4B | GRCh38.p7 | 1:10115924 | CAGTAAAAATATGGC[A/G]TTATAACCTTGTGGG | 10277 |
rs75237846 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10126027 | GATAGAGGGCCAAGC[A/G]CGGTAGCTCATGCCT | 10277 |
rs75240421 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10168906 | CAAAAAAAAAAAAAA[A/G]AGAAGAAGAAAAAGC | 10277 |
rs75247340 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10041350 | CTTTTTTTTTTTTTT[G/T]TTTGATGGAGTTTCG | 10277 |
rs75297997 | snp | A/C | 0.079617 | 0.182947 | intron-variant | UBE4B | GRCh38.p7 | 1:10059829 | TTTTCCACTCCTTTC[A/C]CACAATCAGAATGGC | 10277 |
rs75334915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147633 | TTTTAATTTTGACAA[A/G]TTTTCTTTAAAATTT | 10277 |
rs75392566 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10112741 | TATCACACTCAAAAT[C/T]TGAATCTACCTCTTT | 10277 |
rs75424025 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBE4B | GRCh38.p7 | 1:10110589 | CATGGTAAAGGTACC[A/G]CAGAAGTTATCCGGA | 10277 |
rs75470944 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085575 | GTATTTGGATTTGTT[A/T]TTGTAAACTATGCAG | 10277 |
rs75471522 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10153109 | TTTCTCCTTCAGTTT[G/T]CCAGTTCTCCTGCAG | 10277 |
rs75483938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10049879 | CTGGGCGAGAGAGCA[A/G]AAGACCCTGTCTCAA | 10277 |
rs75509194 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10151981 | GCATATTCTTGGTCC[G/T]GGTGCGGTGGCTCAT | 10277 |
rs75611566 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | UBE4B | GRCh38.p7 | 1:10169337 | GATTTTCTGTATTTG[C/G]TCTTACCTTCGTTAT | 10277 |
rs75644910 | snp | A/C | 0.19646 | 0.2442 | intron-variant | UBE4B | GRCh38.p7 | 1:10034487 | TTGTTGTAAAAAAAA[A/C]AACAACCAAAAAGCA | 10277 |
rs75675743 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10051648 | GGTGGCCTGAATGTA[C/G]TAAGAGGGTGAAGGT | 10277 |
rs75684621 | snp | C/T | 0.00573225 | 0.0532284 | intron-variant | UBE4B | GRCh38.p7 | 1:10179376 | TTTTTCAGTCGTGGG[C/T]TCTCAGTAGATTAGA | 10277 |
rs75685541 | snp | A/C | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10121383 | ACAACAACAAAAAAA[A/C]CATATAATACTTCTT | 10277 |
rs75691022 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10148984 | GAAAACATTTCACAC[A/G]TACCCTTGCATATGC | 10277 |
rs75693735 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10121694 | CCACCGTGCCTGGCC[A/G]TGCTTCCTTTTTTCA | 10277 |
rs75695932 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | UBE4B | GRCh38.p7 | 1:10179154 | GCCACGGAGCCTGTG[A/G]GGCCTGCTGCTGGGT | 10277 |
rs75728541 | snp | C/G | 0.0663309 | 0.169604 | intron-variant | UBE4B | GRCh38.p7 | 1:10123671 | CTCTGGGTGTTTTTT[C/G]TTTGTTTGTTTCCCC | 10277 |
rs75730760 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135346 | CGTGGTGACTCATAC[C/G]TATAATCCCAGCACT | 10277 |
rs75773331 | snp | A/C | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10111957 | GCAAGACTCTGTCTC[A/C]AAAAAAAAAAAAGAA | 10277 |
rs75803150 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10102662 | GTGATCCACTGGCCT[C/T]GGCCTTCCAGAATGC | 10277 |
rs75804384 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10072699 | ATCTCATTAAAAAGT[A/G]AAAGTTTATTTCTTT | 10277 |
rs75821776 | snp | A/C | 0.021333 | 0.101051 | intron-variant | UBE4B | GRCh38.p7 | 1:10169067 | TAGGGTTTATGGTGG[A/C]TTGCAAATAGTCAGA | 10277 |
rs75880248 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055194 | TATGATTAGAATGGG[C/T]TGTGAGTGGGAGAAT | 10277 |
rs75881146 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10106007 | CTTCGAATGGGGACT[C/T]TATCGTCTTGTAAGT | 10277 |
rs75932319 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10156481 | CTGAGCTCAAGTGAT[C/T]TGCCCACCCGGGCCT | 10277 |
rs75994406 | snp | C/T | 0.030665 | 0.119967 | intron-variant | UBE4B | GRCh38.p7 | 1:10105306 | GACGTTAATATCTTA[C/T]ATAACCATGGTACAT | 10277 |
rs76052456 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099907 | GGGCAATTGTTCAAT[C/T]GGGGATAAATGATAT | 10277 |
rs76102619 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | UBE4B | GRCh38.p7 | 1:10134108 | TACTTACTAATTTTG[A/G]GCCTCAGGCAAATCA | 10277 |
rs76119640 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10155233 | TGTTCTCTCTTTCCT[C/G]TTTGCCATGTGTGCC | 10277 |
rs76154155 | snp | C/T | 0.0479149 | 0.147179 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099774 | GGACAGACAAATTGT[C/T]TAACAGAACAGTAAT | 10277 |
rs76200681 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10038792 | TTTTTAAATGCCTGT[C/T]GCGTTAAAAATTTGG | 10277 |
rs76251444 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10134747 | TTTTAAATACTTTTT[A/C]TTGGCTGGTCACAGT | 10277 |
rs76251980 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBE4B | GRCh38.p7 | 1:10136533 | TGTATGCACATTTAA[C/T]GAGGTAGGACAGAAT | 10277 |
rs76270792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10105355 | TACTACTAACTAAAC[A/G]CAAGGCTTTATTTAG | 10277 |
rs76270909 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10048480 | AATGCGGAAGACAAG[A/T]GGACTGAGCCTCCAT | 10277 |
rs76289710 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10080909 | CCAGAGGCTGGGGAA[C/T]GGGGGTGGATGAAGA | 10277 |
rs76304013 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10051322 | AGTGATGTGAAGTGT[A/G]CATGGTGTAGTGACC | 10277 |
rs76304878 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE4B | GRCh38.p7 | 1:10143716 | AGACGAAAGAATCCA[A/G]TTCTTCTGGGATAAG | 10277 |
rs76381708 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | UBE4B | GRCh38.p7 | 1:10160676 | TCCAGGCCAGGTGTG[A/G]TGGCTCATCTCTGTA | 10277 |
rs76397556 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10149019 | TCTTCATTATTCCCT[A/G]TTCATTTCTGGTTGT | 10277 |
rs76404718 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070441 | AGTATCCAGTTAAAA[A/T]TAAAAAAAAAAAAAA | 10277 |
rs76425084 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10086714 | TTTCTCTTTTTTTTT[G/T]GAGATGTAGTCTCAC | 10277 |
rs76477819 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | UBE4B | GRCh38.p7 | 1:10055945 | ACAAAACAAAACAAA[A/C]CCAGAAGTAGAAGTA | 10277 |
rs76489244 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10138849 | CATATCTGTTGAGGA[A/G]ACTAGACTTTTTTCT | 10277 |
rs76556449 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10150323 | AACCTTGGAATTTAA[A/G]CAACTCAAGTCACAT | 10277 |
rs76595484 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBE4B | GRCh38.p7 | 1:10122390 | AGAATACCCAGAGAC[A/G]GCATAAGGCATGATA | 10277 |
rs76682086 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10133133 | AGGGCGTGAGTGCTT[C/T]GGTCCGGGTGAGACA | 10277 |
rs76732246 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | UBE4B | GRCh38.p7 | 1:10168392 | TCATCAATAAGTGAA[A/G]TTCTGTGACTGATTT | 10277 |
rs76752810 | snp | C/G | 0.0130921 | 0.0798413 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180165 | TATTTAAGTGACAAA[C/G]ACGGTCAAAAGCTTA | 10277 |
rs76757997 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | UBE4B | GRCh38.p7 | 1:10127092 | CCACCTATCCAAGTC[C/G]TAGACAGGAGTTAAA | 10277 |
rs76770754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074699 | CTCCTGGTTTTCATG[A/C]ATTCTCTGTATCTGT | 10277 |
rs76779465 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156721 | ATACAATTAATAAAT[A/G]ACATTTAGTTTATTT | 10277 |
rs76799377 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10139570 | AATTATGGATTTAAG[A/T]CAGTTAATATATATA | 10277 |
rs76822479 | snp | A/C | 0.0648419 | 0.167978 | intron-variant | UBE4B | GRCh38.p7 | 1:10172595 | CACACTACTTATCCA[A/C]ATACTATTCATGGCT | 10277 |
rs76842124 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10162001 | TTCTTCACTTTTTCT[C/T]TTTTTTTTTTTTTTG | 10277 |
rs76862201 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10116550 | TGTCGTAATTAATCC[A/G]TATGTGTCTTTTATG | 10277 |
rs76905985 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10061927 | CTTTTTTTTTTTTTT[G/T]TGAGACGAGGTCTCG | 10277 |
rs76936218 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10111969 | CTCAAAAAAAAAAAA[A/G]GAAAGAAAATGCAAA | 10277 |
rs76993995 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | UBE4B | GRCh38.p7 | 1:10077555 | CACCGTGCTTAGCAC[A/G]TGGCAAGCAGTCTGG | 10277 |
rs77011101 | in-del | -/AA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117633 | AACTTAAAAAAAAAA[-/AA]GCCTAGTTATTTGTT | 10277 |
rs77026725 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137339 | GTTCTGTCTGCCTCC[A/C]CCGCCACATCCATGT | 10277 |
rs77046700 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBE4B | GRCh38.p7 | 1:10064028 | ATGGTATTCACAGCT[C/T]GTCATGAGCTTGTTG | 10277 |
rs77055212 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10051620 | ACCACTTTTTCTAAA[A/C]CGTGGAGTGATTGGT | 10277 |
rs77056073 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | UBE4B | GRCh38.p7 | 1:10063337 | GGTATTCTTCCAGGT[A/G]CCTCACACTCAGTAA | 10277 |
rs77075006 | snp | G/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10043442 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCA | 10277 |
rs77120689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048702 | ACTATGGGATTTGGC[C/G]ACATGGAGGCCCTTG | 10277 |
rs77148178 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10160091 | TGAAGTGTAGCTTCT[G/T]TTTTTCTCTACGAAT | 10277 |
rs77151886 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10050721 | TTCAGGACTCCTATT[C/T]TTTTTTTTTTTTTTT | 10277 |
rs77208353 | snp | A/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10097051 | ATCAAAAAAAAAAAA[A/T]AAATAATAATAATAA | 10277 |
rs77236443 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10057520 | CTACTGCACTCAAGC[A/G]CTTCTCCTGCCTGAG | 10277 |
rs77237801 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | UBE4B | GRCh38.p7 | 1:10117162 | TTTTGGTTAAAGTAC[C/G]TGTGATGTCCCTTCC | 10277 |
rs77316933 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10074986 | GTCACAGCTAGCATG[C/T]CCCAAATCAAGCTTT | 10277 |
rs77353882 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10153229 | AGTGCATGTGGGCTG[C/G]GCACGGTGACTCCAG | 10277 |
rs77385930 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBE4B | GRCh38.p7 | 1:10069294 | AGTGCATTTTTCTAG[C/T]ATTTCTCATTTATTC | 10277 |
rs77407699 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085579 | TTGGATTTGTTATTG[A/T]AAACTATGCAGCATG | 10277 |
rs77407959 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10063546 | TTCCTATGCCCATTG[A/C]GCAGGCTTGCTTGTG | 10277 |
rs77452977 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10046847 | GAAAACTTTGATTGT[A/G]GACCGCGGACATTCC | 10277 |
rs77454877 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059922 | AGGGGTGGCAACTCT[G/T]GGGTCTTTGCTAGTG | 10277 |
rs77474955 | snp | G/T | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180775 | CAGGACTTATGTGAC[G/T]TATATTTTGGGGAGA | 10277 |
rs77507361 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10162016 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTTTCACT | 10277 |
rs77546168 | snp | A/C | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10159009 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 10277 |
rs77559290 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | UBE4B | GRCh38.p7 | 1:10057386 | TCGCAACCTTTTTTT[C/T]CTCCCTGAGAAAATA | 10277 |
rs77567553 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | UBE4B | GRCh38.p7 | 1:10141566 | CTTGTTACAGCAGCA[A/G]TAGAAAACTAGCATA | 10277 |
rs77635682 | snp | A/C | 0 | 0 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032346 | CTTAAAAAAAAAAAA[A/C]CCCAGGAAGTATCTC | 10277 |
rs77723220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155489 | TTTAGCACAGGTCCC[C/T]CTGGCTACTGTGCTG | 10277 |
rs77727478 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | UBE4B | GRCh38.p7 | 1:10072893 | AGTTGCGTAAAGGGG[G/T]TGCTAAGAGAACTGC | 10277 |
rs77731146 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBE4B | GRCh38.p7 | 1:10140999 | AATAATACTGAATTC[A/G]GGGTCTCTGGTAGGT | 10277 |
rs77797389 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10141851 | CAGCTAGTTCTCCCA[A/G]ACTCCTCCATTTGAA | 10277 |
rs77838704 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10102551 | AAGTAGCTCCGAGTA[A/G]CCAGGCCCGCAACCG | 10277 |
rs77892776 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10068853 | ATTATCCTCTACTGA[G/T]AGCCCTGCTGTGGGC | 10277 |
rs77897515 | snp | G/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10060778 | CAATTTTTTTTTTTT[G/T]GGAGCCAGTCTCACT | 10277 |
rs77898517 | snp | C/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10109212 | AGGGGGAACGGGGGG[C/G]CCGGGGGGACAGACA | 10277 |
rs77939321 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | UBE4B | GRCh38.p7 | 1:10161898 | CTTAGATTGGCTTAG[A/G]TTTATTGATTCTGTT | 10277 |
rs77949343 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UBE4B | GRCh38.p7 | 1:10143367 | GATGATGCCAGTTTA[C/G]TCCAGCCTGGGCAAT | 10277 |
rs77958155 | snp | A/C/T | 0.031451 | 0.121469 | intron-variant | UBE4B | GRCh38.p7 | 1:10111249 | CTACACACACACCCC[A/C/T]ACACCAAGCATACAT | 10277 |
rs77980262 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | UBE4B | GRCh38.p7 | 1:10087912 | CCCTTCTCCCCTGCT[A/T]TGTATTTAATCTCTT | 10277 |
rs77985758 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038772 | TCCTCCCACTCCCAA[A/C/T]TTTTTTTTTAAATGC | 10277 |
rs78003405 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10060780 | ATTTTTTTTTTTTTG[G/T]AGCCAGTCTCACTCT | 10277 |
rs78004661 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | UBE4B | GRCh38.p7 | 1:10073089 | TCAACCAAAACATCT[A/G]TTAGTAATAAAGAAG | 10277 |
rs78011570 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10162015 | TTTTTTTTTTTTTTT[G/T]GAGACGGAGTTTCAC | 10277 |
rs78038419 | snp | A/C | 0.0330477 | 0.124224 | intron-variant | UBE4B | GRCh38.p7 | 1:10147137 | CTCCTTGGCTGGGCT[A/C]TGTTGTCTTTATTGT | 10277 |
rs78062225 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10034431 | AAAGGAGTTATACAG[A/T]TCTACTTCTTGATGT | 10277 |
rs78118411 | snp | C/T | 0.00697736 | 0.0586515 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119557 | TCTGAGCAACATCCG[C/T]TCACAGTGCATATCC | 10277 |
rs78150027 | snp | A/G | | | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10144968 | TTGAAAAATAATGAA[A/G]GCCAATGGAAAGATT | 10277 |
rs78193965 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10151764 | AACCATTCCACCTAC[G/T]GGTCTCTGATGATTC | 10277 |
rs78221419 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099625 | CCTCAGGCTGATTCC[C/T]AAGTATGTGTAGAAG | 10277 |
rs78278070 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10141177 | GCATCTCAAAGGTGC[C/T]CACATCCTGGTCTCG | 10277 |
rs78285636 | snp | C/G | 0.046775 | 0.145601 | intron-variant | UBE4B | GRCh38.p7 | 1:10080669 | ACCTAAATAATCCAT[C/G]TTCAGATGAATGGGA | 10277 |
rs78312337 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10065508 | CTGCAGGGGTAGTTT[C/T]GGCCCTGTGACTGTT | 10277 |
rs78355390 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBE4B | GRCh38.p7 | 1:10109480 | TGTCCCTTGTTGGCC[A/G]TTACAGTGAACTGTG | 10277 |
rs78371026 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10062318 | GATGTGTGTTTTTTT[G/T]TTTGTTTCTTTTGAG | 10277 |
rs78413623 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10045328 | CACATTTTGTAACTG[A/T]ACATACAGTTAGGAG | 10277 |
rs78438768 | snp | A/C | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10124891 | AGCACTTTGGGAGGC[A/C]GAGGCAGGTGGATCG | 10277 |
rs78468981 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10118348 | GTTTTTTGTTTTTTT[G/T]GTTTTTTGAGATGGA | 10277 |
rs78508549 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBE4B | GRCh38.p7 | 1:10087941 | TTAGATCAGTATGAA[C/T]TCACACACATTTATT | 10277 |
rs78513675 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10062317 | CGATGTGTGTTTTTT[G/T]GTTTGTTTCTTTTGA | 10277 |
rs78519671 | snp | A/C | 0.0112395 | 0.0741175 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10101105 | TGTCTTTTGTACTTT[A/C]AGCATGTCCCAGGTG | 10277 |
rs78526627 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10065561 | AATTGAATGTGTCAC[A/C]GCTGGGCCAGTGTGG | 10277 |
rs78539482 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10101955 | TTTGAATATCACCTG[A/G]GCTTAGTGCTCTGCA | 10277 |
rs78702145 | snp | A/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10039598 | CCATGCCCTGCTGAT[A/T]TTTTTTTTTTTTTGT | 10277 |
rs78708465 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10153027 | TAGCTCTGGGGGTAC[A/G]AGACAAAGCTGAAAA | 10277 |
rs78737349 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | UBE4B | GRCh38.p7 | 1:10154385 | ATCTAAAAAAATTTT[A/T]AAAAAAAAGAGTGGA | 10277 |
rs78739590 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10057818 | AGTATTTTGTGCTTT[A/G]TTTTTGAGATATTTA | 10277 |
rs78744911 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | UBE4B | GRCh38.p7 | 1:10164544 | ATGTTGGAATGCAGG[C/T]CTATAGCACATTCTC | 10277 |
rs78785018 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10067088 | TTTTGTGGGTGTTTT[C/T]CCCCACAAACTGCTA | 10277 |
rs78798966 | snp | C/G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10043664 | GAGGCGGGTGGATCA[C/G/T]GAGGTCAGGAGATCG | 10277 |
rs78868627 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE4B | GRCh38.p7 | 1:10077818 | TATTTCAAATGTACA[C/T]GATAACATAACTAGT | 10277 |
rs78877530 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | UBE4B | GRCh38.p7 | 1:10159996 | CATGTTCCTGAGATC[A/G]AGGCCTCCTGCACTT | 10277 |
rs78897857 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE4B | GRCh38.p7 | 1:10127827 | AATAAGAGCTACAGC[A/G]CAACAGTTGAACAGA | 10277 |
rs78925586 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10063349 | GGTACCTCACACTCA[A/G]TAATCTAATCATAAC | 10277 |
rs78925707 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10072334 | CAGCTCTTTAAAATC[C/T]TCCAAGCAGTAGTTT | 10277 |
rs78928169 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10128669 | TTGAGGCTGCCTGAA[C/T]CTCAAAGGCATCTCA | 10277 |
rs78936176 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | UBE4B | GRCh38.p7 | 1:10051179 | CTGGCTCTTACCTGG[A/T]TTTTATTTGGAGCAA | 10277 |
rs78946424 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135347 | GTGGTGACTCATACC[C/T]ATAATCCCAGCACTT | 10277 |
rs79015239 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10156801 | ATGATAGGTGTTAAT[G/T]ATCTTATTTTATTTT | 10277 |
rs79056809 | snp | A/G | 0.375 | 0.216506 | intron-variant | UBE4B | GRCh38.p7 | 1:10150185 | CAATGAGCAGAGATC[A/G]TGCCACTACACTCCA | 10277 |
rs79086613 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | UBE4B | GRCh38.p7 | 1:10159045 | AAAGAAAAGATCCTA[C/T]AAATATGCTGAGATG | 10277 |
rs79123143 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | UBE4B | GRCh38.p7 | 1:10096230 | TGGAATATTTCATAC[A/G]GGTAAGCCAAATAAA | 10277 |
rs79153118 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10119990 | TCCATGTATAACACG[A/G]TCAATTTCTGTTACT | 10277 |
rs79224536 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10134610 | TAGCACCTGCTAATA[C/T]AGAATTAATGGAATG | 10277 |
rs79249418 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10137900 | TCTCTGTATCTACCT[C/T]GCTTAAATCACTTAC | 10277 |
rs79271891 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10113082 | TTAATTGGCTCATGG[A/T]ACCTCAGGCTGTTCA | 10277 |
rs79283712 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | UBE4B | GRCh38.p7 | 1:10109055 | AGATCTAAATTCTCT[C/T]CCTACTAGGAGGAAT | 10277 |
rs79286153 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10157028 | AAAGTGAAAAAAAAA[A/T]TTTTTGAGACAGAGT | 10277 |
rs79293532 | snp | A/G/T | 0.00034091 | 0.0130516 | intron-variant | UBE4B | GRCh38.p7 | 1:10134943 | CCATCTCAAAAAAAA[A/G/T]TTTTTTTAATGTTTA | 10277 |
rs79333089 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10156489 | AAGTGATCTGCCCAC[C/T]CGGGCCTCCTGAAGT | 10277 |
rs79383368 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10042151 | GAGTGGAGCTCATCA[A/G]GTAGCCCCAAGCTCT | 10277 |
rs79388192 | snp | A/C | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10168891 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 10277 |
rs79498113 | snp | G/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10089716 | ATTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCA | 10277 |
rs79583882 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10037513 | TATTAATTCTATAAT[C/T]TACTCATGTGTTGTT | 10277 |
rs79635289 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10126506 | GCTCCAAATGTATGG[A/G]TTTTGTTGAATTACT | 10277 |
rs79653521 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10151943 | TTCCAAAGTGTGGGT[A/G]AAACAGGGAGCTTGT | 10277 |
rs79704569 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10139027 | TGCATCTGTTCAAAA[A/G]AAAGCCTGACCTGTA | 10277 |
rs79744368 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | UBE4B | GRCh38.p7 | 1:10108808 | AAAGTGTCTTTTTCA[C/T]GTAGATAAAATCCTA | 10277 |
rs79746975 | snp | A/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10123455 | AAAAAAAAAAAAAAT[A/T]ACTGTCTTGGAAGGT | 10277 |
rs79758840 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | UBE4B | GRCh38.p7 | 1:10109206 | AGTGGCAGGGGGAAC[C/G]GGGGGGCCGGGGGGA | 10277 |
rs79774214 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10083412 | TTGAGTCTTTAATGA[A/G]CATTATGATTGCTTA | 10277 |
rs79780579 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10145657 | CTGCCTTATGCAGGG[C/T]CCTCCTCACCTGCTG | 10277 |
rs79790757 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | UBE4B | GRCh38.p7 | 1:10132582 | CTAGGAGTGGGGGTA[C/T]AGTATTGAACAAGGT | 10277 |
rs79803538 | snp | G/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032065 | GCTGATTTTTTGTAT[G/T]TTTTAGTAGAGACGG | 10277 |
rs79814128 | snp | G/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10092649 | CCTGACAAACATGGT[G/T]AAACCCCATCTCTAC | 10277 |
rs79817253 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10159253 | AAGACTTTTCATATA[A/C]CTACCTGAAATCTGA | 10277 |
rs79872859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074315 | TTCCTTTCTCTCTCT[C/T]GCTTCATCAGATTTT | 10277 |
rs79873809 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10050723 | CAGGACTCCTATTCT[C/T]TTTTTTTTTTTTTTT | 10277 |
rs79917267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090129 | TGTGTGTGTGTGTGT[G/T]TTTTTTTTTAGGCAT | 10277 |
rs79945070 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | UBE4B | GRCh38.p7 | 1:10049730 | ACATAGGGAGACCCC[A/G]TATGTCCAAAATGGC | 10277 |
rs79949214 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10039146 | GAGGAGATAGATAGG[A/T]ATCCAACAGTTATAG | 10277 |
rs79966104 | snp | C/T | 0.492775 | 0.059668 | intron-variant | UBE4B | GRCh38.p7 | 1:10080605 | CTGAAGAGATACCTC[C/T]ACTCATGTTCATTGC | 10277 |
rs79980202 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | UBE4B | GRCh38.p7 | 1:10083492 | TAAGTTGTCTTTGGC[A/T]AAGAATGCTATCCAC | 10277 |
rs79982090 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | UBE4B | GRCh38.p7 | 1:10175255 | GTCTTTATGGGCAGA[C/T]GCCAGTTCCATGGAC | 10277 |
rs80010879 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | UBE4B | GRCh38.p7 | 1:10160596 | TGACTGTCATCAGCC[A/G]TGCAAGGTGGCTCCA | 10277 |
rs80072425 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10057734 | GACCCTGTCTCACAG[A/G]AAAAAAAAAAAAAGA | 10277 |
rs80094534 | snp | A/G | 0.0429648 | 0.14013 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171398 | TAACCACAGTGGCCA[A/G]GGAACTCGTCTGGTG | 10277 |
rs80105625 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10177925 | GTTCAGATTTGCCTA[C/T]GACTGCACAGCTGGT | 10277 |
rs80108048 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10063452 | GAAATCTAGATTATT[A/C]TTCTTCCTCACTTTT | 10277 |
rs80149311 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099615 | TTAAGGAATTCCTCA[G/T]GCTGATTCCTAAGTA | 10277 |
rs80164123 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10147205 | TATCAAGAATTCACT[G/T]CTCTGCAAGGCGCAG | 10277 |
rs80192267 | snp | A/C | 0.030665 | 0.119967 | intron-variant | UBE4B | GRCh38.p7 | 1:10117662 | GTTTGATTATCCCCA[A/C]CCCTGGAGCATTCAT | 10277 |
rs80242219 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10061907 | CTGGCTTTATCTTCT[C/T]TTTTCTTTTTTTTTT | 10277 |
rs80302867 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10136416 | TTGAGGCTGCAGTGA[C/T]CTGTGATCTTACCAC | 10277 |
rs80334055 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10162014 | CTTTTTTTTTTTTTT[G/T]TGAGACGGAGTTTCA | 10277 |
rs111257057 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10067619 | AAATTAATTAGATAC[A/G]CTTTTTTTTTTTTTT | 10277 |
rs111297331 | in-del | -/G | 0.467132 | 0.12391 | intron-variant | UBE4B | GRCh38.p7 | 1:10090127 | CCTGTGTGTGTGTGT[-/G]TTTTTTTTTTTAGGC | 10277 |
rs111329090 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10160876 | TGAGCCCTGGAGGTC[A/G]AGGATGCAGTGAGCT | 10277 |
rs111337758 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10132626 | GCTTTTGTGGAGCCC[A/G]TGTTCCACAGAATAA | 10277 |
rs111341127 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10038556 | GGCTTAGAAGTGATG[G/T]GGTTGGAATTCAAAC | 10277 |
rs111364496 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | UBE4B | GRCh38.p7 | 1:10148430 | TGAGGTCAGGAGTTC[A/G]AGACCATCCTGGCCA | 10277 |
rs111395039 | in-del | -/TG | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10175514 | AATTAGCCAGGCGTG[-/TG]GTGGCGGGCGCCCGT | 10277 |
rs111402432 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10042955 | ATGCCAAGCATGGTT[A/G]GAGCCTTCTGTGCAA | 10277 |
rs111406639 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10155804 | GAGACAGGTGAATCA[C/G]TTGAGGCCAGGAGTT | 10277 |
rs111424650 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10129741 | CTGCAGCCTACGCCT[C/T]CTGGGTTCAAGTGAG | 10277 |
rs111536506 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10164339 | GGCAACAGAGCGAGA[C/T]TCCGTCTCAAAAAAG | 10277 |
rs111557887 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10166882 | GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC | 10277 |
rs111584262 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10163663 | ACAGAGTGAGACTCC[A/G]TCTCAAATAAATAAA | 10277 |
rs111586532 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032211 | GTATTCTTGTGCACC[A/G]GAGGATGGTTTTCCC | 10277 |
rs111587346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169343 | CTGTATTTGCTCTTA[A/C]CTTCGTTATGTGACT | 10277 |
rs111690617 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100617 | TGGAGTGCAATGGTG[C/T]GATCTCGGCTTACCG | 10277 |
rs111738540 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10121441 | TAAGAGACAGAATCT[C/G]ACTCTGTTGTCTAGG | 10277 |
rs111742206 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | UBE4B | GRCh38.p7 | 1:10044303 | CAAATGATCGGCTTG[C/T]CTCGGCCTCCCAAAG | 10277 |
rs111807870 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10160575 | AATTCTGGAATATTT[A/C]GCACTTGACTGTCAT | 10277 |
rs111855823 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10153519 | AAAAAAAAAAAAAAA[G/T]GGTAAAAAGACTGGG | 10277 |
rs111893655 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | UBE4B | GRCh38.p7 | 1:10086920 | GTGTCAAACTCCTGA[C/T]CTCGGCCTCCCAAAG | 10277 |
rs111904134 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10119341 | TCTGACATCAGTTTC[C/T]GCAGAGGCAGTACAC | 10277 |
rs111908496 | in-del | -/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10068356 | TCTTTTTTCTTTTTC[-/T]TTTTTTTTTTTGAGC | 10277 |
rs111911855 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UBE4B | GRCh38.p7 | 1:10040418 | CAGGCCTCCGGCTAA[C/T]TTTTGTATATTTTGT | 10277 |
rs111941781 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10161851 | ATACTTCCTTGGTCG[C/T]TTATGAGGCCCTTGA | 10277 |
rs112020330 | in-del | -/AT | 0.0596104 | 0.162024 | intron-variant | UBE4B | GRCh38.p7 | 1:10102065 | ATCCTTTAGCAACAC[-/AT]GTTAATGATTATTGG | 10277 |
rs112042106 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105562 | GATTTTAATGGAAGT[A/G]CTAATGATGTCCACT | 10277 |
rs112052140 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10139709 | TCCTTATTATTTCTG[C/G]TTTTATTTATTTATT | 10277 |
rs112063136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129600 | CTCTCAACTGTTACA[A/T]TTTTGTTAGACACGT | 10277 |
rs112067924 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10058984 | TGGGCGCGGTAGCTT[A/G]TGCCTGTAATCCCAG | 10277 |
rs112077178 | in-del | -/GAGA | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10155065 | TCACTGTGGCTTCAG[-/GAGA]GAGAGAGAGAGAGAG | 10277 |
rs112145351 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10142437 | CAACACTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 10277 |
rs112155920 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | UBE4B | GRCh38.p7 | 1:10174331 | CCGGGAGGCAGAGGT[C/T]GCAGTGAGCTGAGAT | 10277 |
rs112214353 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10150450 | AATTTTTATGTTTTG[A/G]TAGTGATGATCTTTT | 10277 |
rs112229100 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10082741 | GTTTGCTGCACCTAT[C/G]AACTCATCATCTAGA | 10277 |
rs112271527 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10175624 | CCACTGCACTCCAGC[C/T]TGGGCGACAGAGCGA | 10277 |
rs112308237 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBE4B | GRCh38.p7 | 1:10129855 | ATGGAGTTTTACCAT[A/G]TTGGCCAGGCTGGTC | 10277 |
rs112310397 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10073150 | CTCTGAGAAGCTCTG[A/G]TGGTCTTCTGGTAGG | 10277 |
rs112313350 | snp | A/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10081051 | TTAAAATTCTACTTT[A/T]TAAAAACAACAATAT | 10277 |
rs112317184 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174609 | CGGGAGGCTGAGGCA[A/G]GAGAATCGCTTGAAC | 10277 |
rs112322184 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10047668 | TGGCTAATTTTTTCT[A/G]TTTTTAGTAGAGATG | 10277 |
rs112359940 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135601 | AATTAGCGGGTGTGG[C/T]GGCACGCACCTGTAA | 10277 |
rs112380015 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10133754 | CATCTCTACAAAATA[C/T]ACAAAAGTCATCTGG | 10277 |
rs112391309 | snp | C/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10136452 | TGCACTGCAGCCTAG[C/G]TGACACTAGGTGACA | 10277 |
rs112410336 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE4B | GRCh38.p7 | 1:10145473 | GGCGTGATGGCGGGC[A/G]CCTGTAGTCCCAGCT | 10277 |
rs112410575 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10135490 | ACGCCTGTAATCCCA[G/T]CACTTTGGGAGGCTG | 10277 |
rs112438859 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10175607 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 10277 |
rs112443182 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175568 | AGGCAGGAGAATGGC[A/G/T]TGAACCTGGGAGGTG | 10277 |
rs112449674 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10046732 | TGGACATTGGAGGCT[A/G]TCCTTTTTGTAGGGC | 10277 |
rs112464846 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10175582 | CGTGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 10277 |
rs112470676 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10117750 | CTAGGAACTTAGGAT[A/G]TGTCGATGAACAAAA | 10277 |
rs112475314 | in-del | -/A | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10111956 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAGA | 10277 |
rs112506776 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10074340 | GATTTTCCATCTCAT[A/G]TGGCCTTTTTTTTTT | 10277 |
rs112515234 | snp | A/C/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10175630 | CACTCCAGCCTGGGC[A/C/G]ACAGAGCGAGACTCC | 10277 |
rs112550785 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10075565 | TGGGCATTCCCTAAA[C/T]GGTTAGTTCTTGCCC | 10277 |
rs112582067 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | UBE4B | GRCh38.p7 | 1:10068114 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 10277 |
rs112585126 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | UBE4B | GRCh38.p7 | 1:10109912 | CACCTCGGCCTCCCA[A/G]AGTCTCAAACTTCTG | 10277 |
rs112615334 | snp | C/T | 0.0115144 | 0.0749975 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181394 | CTTATTCATGTCAGT[C/T]TCGACATTTGGTTCT | 10277 |
rs112635498 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | UBE4B | GRCh38.p7 | 1:10139368 | TGTACTCCAGCCTGA[A/G]CAAGAGTGAGACTCT | 10277 |
rs112687680 | snp | C/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10175587 | ACCTGGGAGGTGGAG[C/G]TTGCAGTGAGCCGAG | 10277 |
rs112703239 | in-del | -/A | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10151162 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 10277 |
rs112714734 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052128 | CTGGAGTGTAGTGGT[G/T]CCATCTTGGCTCACT | 10277 |
rs112749844 | in-del | -/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10176493 | TTCCATTCTTTTTCA[-/T]TTTTTTTCTTTGGTT | 10277 |
rs112787341 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10128331 | GTGCCATTATTGATG[C/T]TTGCATAATAACGAG | 10277 |
rs112787694 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10152792 | GAAAGGGCAAGACTC[C/T]GTCTCAAAAAAGAAA | 10277 |
rs112817721 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168785 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10277 |
rs112852360 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10141451 | GGAAACTTGTTCTCC[C/T]CTAGAGCCTCCAGAA | 10277 |
rs112860894 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10154367 | AGGTTGTAGTTAGCC[A/G]AGATCTAAAAAAATT | 10277 |
rs112866835 | in-del | -/T | 0.437118 | 0.165792 | intron-variant | UBE4B | GRCh38.p7 | 1:10036083 | ACTCCTATAAATTAC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs112907042 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10063679 | GGAGGCCAAGTCAGG[C/T]GGATCACTTGAGGTC | 10277 |
rs112930377 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10038173 | TGATCCGAGGTACTC[A/G]GGAGGCTGAGGCAGG | 10277 |
rs112945371 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10159499 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 10277 |
rs112961864 | in-del | -/AAAAG | 0.0115144 | 0.0749975 | intron-variant | UBE4B | GRCh38.p7 | 1:10092535 | TGAGACCCATTTCTT[-/AAAAG]AAAATAAGGAGGCCA | 10277 |
rs112962165 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10102146 | GTTGCACTGTAGCCT[C/T]CTAGTGGTGCAGTGC | 10277 |
rs112973146 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBE4B | GRCh38.p7 | 1:10174957 | GTTTGCTTTGGTATG[C/T]CTTAGTTTGGTTTGG | 10277 |
rs113004852 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10038557 | GCTTAGAAGTGATGG[G/T]GTTGGAATTCAAACC | 10277 |
rs113006833 | snp | C/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10175565 | CTGAGGCAGGAGAAT[C/G]GCGTGAACCTGGGAG | 10277 |
rs113007946 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10077184 | GTCCAAAGCCAAGGT[A/G]TTGGTAGGGCGATGC | 10277 |
rs113020505 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10168368 | GTTCTGGAAATTTTA[A/G]GATCACAGTCATCAA | 10277 |
rs113030241 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10145595 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 10277 |
rs113085516 | snp | C/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10120754 | GAGGCACGAGAATTG[C/G]TTGAACCCGGGAGGT | 10277 |
rs113102667 | snp | C/G/T | 0.0703144 | 0.176471 | intron-variant | UBE4B | GRCh38.p7 | 1:10175447 | ACAAGGTCAGGAGAT[C/G/T]GAGACCGTCCTGGCT | 10277 |
rs113123029 | snp | G/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10089758 | ATCCTGGAGGGCAGT[G/T]GCTCAATCTCGGCTC | 10277 |
rs113142133 | in-del | -/AT | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10111086 | CACACACACACACAC[-/AT]ACACACAGTCTTTCC | 10277 |
rs113183808 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBE4B | GRCh38.p7 | 1:10175724 | GTCACACTTCCCCCA[C/T]GCAGTCAGTCTTTCC | 10277 |
rs113223852 | in-del | -/AT | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10050739 | TTTTTTTTTTTTTTT[-/AT]AGAGGTGGAGTTTCA | 10277 |
rs113284479 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE4B | GRCh38.p7 | 1:10101578 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAAGCTC | 10277 |
rs113304383 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094402 | ATTTTGCAGGGAACA[C/T]CCGTATACTCACCAT | 10277 |
rs113368482 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10134517 | AACTCCATCTCAAAA[A/G]AAAGAAAAGAAAAGA | 10277 |
rs113386648 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10175612 | GCCGAGATCGCGCCA[C/T]TGCACTCCAGCCTGG | 10277 |
rs113406947 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | UBE4B | GRCh38.p7 | 1:10047547 | GCCCAGGCTGGAGTG[C/T]AGTGGCGTGATCTCG | 10277 |
rs113414772 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | UBE4B | GRCh38.p7 | 1:10174071 | ACAAACACACATGTG[C/T]CAGTGACACATGGAG | 10277 |
rs113433148 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10131348 | CAGGCATGGCAGCGC[A/G]TGCCTGTAATCCCAG | 10277 |
rs113445913 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10156948 | ACGATGTAGGAGGAT[C/T]GCTTGAGGCAGGAAT | 10277 |
rs113448784 | snp | C/T | 0.187053 | 0.241946 | intron-variant | UBE4B | GRCh38.p7 | 1:10054894 | GGGTTCAAGCGATTC[C/T]CCTGCCTCAGCCTCC | 10277 |
rs113452335 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBE4B | GRCh38.p7 | 1:10043675 | CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 10277 |
rs113503105 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10150090 | GATTTTAAAATAAGG[A/G]CCAAAAGTAAATGGA | 10277 |
rs113530649 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10172220 | CTAAGCTGTCCCTGC[A/G]TGATCTTCTAGTCAT | 10277 |
rs113544180 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10063223 | CAGTGAGCTGAAACC[A/G]TGCCTCTGCACTCCC | 10277 |
rs113586345 | snp | C/T | 0.108755 | 0.206276 | intron-variant | UBE4B | GRCh38.p7 | 1:10088740 | GCTGGGGGACAGTGA[C/T]GCAATCATGGCTCAC | 10277 |
rs113642574 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10145208 | TACCTTACTTATATG[G/T]GTATATAATGATTTC | 10277 |
rs113644846 | in-del | -/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10089702 | GTTTTACTTTTGTAA[-/T]TTTTTTTTTTTTTTT | 10277 |
rs113685306 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10175577 | AATGGCGTGAACCTG[A/G]GAGGTGGAGCTTGCA | 10277 |
rs113701369 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10060508 | GCAGCCCATGACTGT[A/G]TTTCCTCTCTGACTT | 10277 |
rs113727112 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10120786 | GAGGTTGCAGTGAGC[C/T]GAGATCACGCCACTT | 10277 |
rs113765259 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10035719 | CCAGAGATAGTTTTT[A/T]TATTTTTTTTTATTT | 10277 |
rs113766750 | in-del | -/A | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10089504 | GAGAACATGTCTCTG[-/A]AAAAAAAAAAAAAGT | 10277 |
rs113794437 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | UBE4B | GRCh38.p7 | 1:10174224 | GATGATGAAACCCCA[C/T]CTCTACTAAAAATAC | 10277 |
rs113826563 | snp | C/G | 0.130351 | 0.219509 | intron-variant | UBE4B | GRCh38.p7 | 1:10037150 | TTCCTGCGTCAGCCT[C/G]CCAAGTAGCTGGAAT | 10277 |
rs113845351 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBE4B | GRCh38.p7 | 1:10142596 | GAATCGCTTGAACAC[A/G]GGAGACGGAGGTTGC | 10277 |
rs113862880 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10161484 | GCTAAGAAATGGGTT[A/G]AGAAGTCTTTGAAAA | 10277 |
rs113896874 | snp | C/T | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10082044 | CAAATTTGCTTGATA[C/T]GTTTTATCTATTTTA | 10277 |
rs113935979 | snp | A/G | 0.5 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10155726 | AGTATTCTAGCTTAG[A/G]AAATGCTCAAGTTAG | 10277 |
rs113941904 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180198 | GGACAGGTTTTATGG[C/T]TGCTTGTGTAATAAA | 10277 |
rs113948577 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBE4B | GRCh38.p7 | 1:10130176 | CCTCCTGGGTTCAAG[C/T]GATTCTCTTGGCCTC | 10277 |
rs113950298 | in-del | -/T/TTT | 0.402642 | 0.208029 | intron-variant | UBE4B | GRCh38.p7 | 1:10142044 | GTCATTTTTTTTTTT[-/T/TTT]CTATAAGCTCCACCA | 10277 |
rs114056989 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | UBE4B | GRCh38.p7 | 1:10114574 | GTTGCTATAAAGACA[A/C]AATAATTGGCCAGGT | 10277 |
rs114105600 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032217 | TTGTGCACCGGAGGA[C/T]GGTTTTCCCCCACTG | 10277 |
rs114110191 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093873 | CTAATTTTTGTATTT[G/T]AACTAGAAACAGGGT | 10277 |
rs114117645 | snp | A/C/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10062020 | GTTAAAGCTTTTCTT[A/C/G]TGCCTCAGCTTCCTG | 10277 |
rs114142295 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBE4B | GRCh38.p7 | 1:10046626 | TCTGGTCTCTTGAAG[A/G]AGCTCCCTTGTGCCT | 10277 |
rs114159428 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10144401 | CCAAATCTGTAGTGC[C/T]ATCCATTCAAAGACA | 10277 |
rs114161786 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10069322 | TTCAGCAGATATTTA[G/T]AGAGTACCTACCATG | 10277 |
rs114168698 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10177129 | CTAGGTCATATCAGA[C/T]GATACATGTATCATT | 10277 |
rs114189111 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10175903 | TGGCATGTAGTACAG[A/T]CACAGCGTTGCACAG | 10277 |
rs114192263 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10093131 | ACAATTTGTAATTAT[A/G]TGTTTAATTTTATAA | 10277 |
rs114212496 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10168016 | GGACATGTGGCAGGC[A/G]GTTCTGTCATTCCCT | 10277 |
rs114227524 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10139355 | AAGACCGAGCCACTG[C/T]ACTCCAGCCTGAGCA | 10277 |
rs114228583 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10164722 | TTTCTACCTCCCACT[A/G]CCCTGGCTGTTCCTG | 10277 |
rs114230585 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10074904 | CAACGTGGACCTGCT[C/G]CTTGAACCTCAGATT | 10277 |
rs114265719 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBE4B | GRCh38.p7 | 1:10082630 | TCCTATTAAGAAGGC[A/G]ACTTTTTTTTTTTTT | 10277 |
rs114291761 | snp | C/T | 0.0332957 | 0.124657 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158414 | CACAATTCGCTATCA[C/T]ATTAGCACCATTTTT | 10277 |
rs114344246 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10153242 | TGGGCACGGTGACTC[C/T]AGCTAATAATCCTAG | 10277 |
rs114393439 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099389 | AGGTGCCATTCACAA[C/T]TTCATTAAAAAGTAT | 10277 |
rs114399015 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | UBE4B | GRCh38.p7 | 1:10120572 | TTTACAGGCCAGGCT[C/T]ATGCCTGTAATCCTA | 10277 |
rs114489388 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10136251 | GCTGAGGTGGGAGGA[G/T]AGCTTGAGCCCAGGA | 10277 |
rs114515417 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10108021 | ACCCTTCATTTATCT[A/C/G]TTGCGAGAATGTTAT | 10277 |
rs114525499 | snp | C/T | 0.0221141 | 0.102801 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031020 | ACCCCAAAGGCCACA[C/T]GGTGTATTGCTCCAC | 10277 |
rs114554959 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | UBE4B | GRCh38.p7 | 1:10122605 | ATTGTGTAAAGCCAG[A/G]TGAAAATGCAGATAT | 10277 |
rs114572380 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10148282 | GAGTTGCACAAAATG[A/G]CCAAATAGGACCTTT | 10277 |
rs114597380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10102878 | TTAAATCAGAATAAC[A/G]TATTCCTATTGAAAC | 10277 |
rs114627513 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10092887 | CCCTGGTGTTTAGAG[A/T]TTGAGGAGCACTTGT | 10277 |
rs114631287 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10161078 | GTGCTTGTTCCCTGG[C/G]ATTTGCTGTGGCATT | 10277 |
rs114633632 | snp | A/C | 0.0267878 | 0.112589 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181375 | ATTTTTAAAAGAAAA[A/C]TTTCTTATTCATGTC | 10277 |
rs114762967 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | UBE4B | GRCh38.p7 | 1:10143601 | TACAACGTCCCTTTC[G/T]CCATGGGAGATCACA | 10277 |
rs114766396 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | UBE4B | GRCh38.p7 | 1:10038872 | GAGGTCGAGGCAGGC[A/G]GATCACGTGAAACCC | 10277 |
rs114777012 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | UBE4B | GRCh38.p7 | 1:10081581 | TGGCACGTGCCACCA[C/T]GCCTGGCTAATTTTT | 10277 |
rs114793139 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBE4B | GRCh38.p7 | 1:10102707 | TGAGCCACCACGCCC[A/G]GCCATCTTTGCTCTT | 10277 |
rs114817195 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10111513 | ACACACACGCACCCA[C/T]GCACGCACACCGTCG | 10277 |
rs114826600 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | UBE4B | GRCh38.p7 | 1:10165742 | ACTCCTTCAGATATA[A/C]CCTCCCTCAGGGATA | 10277 |
rs114852861 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE4B | GRCh38.p7 | 1:10175703 | AAAAAAATAAAAATC[C/T]CATCAGTCACACTTC | 10277 |
rs114892867 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10143633 | GTTCACAGGTTCCCT[C/T]GAAGGATTCGGATGC | 10277 |
rs114945189 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10036959 | GTATAACCAGACTGG[C/T]AGCTTTAGGAACTTT | 10277 |
rs114958195 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10098787 | CTACCAAAAAACTAC[A/C]GCAACTCTCCTATTC | 10277 |
rs114975679 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | UBE4B | GRCh38.p7 | 1:10079238 | CTGGAGGGCAGTGAC[A/G]TAGTCTGCCTCCCGG | 10277 |
rs114982076 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10077274 | ATTTCTTGGCTTGTG[A/G]CAACATAACTCCAGT | 10277 |
rs114982490 | snp | G/T | 0.0803491 | 0.183626 | intron-variant | UBE4B | GRCh38.p7 | 1:10041654 | TTATAGCATTCTTAC[G/T]GTCCCTTCTGAGATA | 10277 |
rs115020324 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10122607 | TGTGTAAAGCCAGGT[A/G]AAAATGCAGATATGT | 10277 |
rs115056809 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10152764 | GATCACACCAGTGTG[C/G]TCCAGCCTAGGAGAA | 10277 |
rs115059827 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | UBE4B | GRCh38.p7 | 1:10162048 | TTGTCGCCCACGCAG[A/G]AGTACAGTGGTGCGA | 10277 |
rs115093897 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10043729 | CAACGCGCTGGGCCG[G/T]GATGCTTCTTATAAA | 10277 |
rs115095456 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | UBE4B | GRCh38.p7 | 1:10064623 | ACTCTCTATCACCTC[A/G]TCTCTTTGTCACTTC | 10277 |
rs115148899 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | UBE4B | GRCh38.p7 | 1:10092872 | AGAAGGAATGGAGTC[A/C]CCTGGTGTTTAGAGA | 10277 |
rs115206094 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10159749 | TTGCAACCCATGTTA[G/T]ATCTTTGATCAAATC | 10277 |
rs115216249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061854 | TGTCAGTTACTTACT[A/G]TGTTGCTATACGTGT | 10277 |
rs115298179 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099443 | ATTTAGCAAAAGAAG[C/T]ATAAAATTTTTATAG | 10277 |
rs115307556 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10141593 | CATAACACATTAGCA[A/G]ATCTTGCCATTTTTT | 10277 |
rs115337275 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBE4B | GRCh38.p7 | 1:10047091 | CCATTCTTCCATCCT[A/G]CAGTATCTGTGCCCA | 10277 |
rs115384680 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | UBE4B | GRCh38.p7 | 1:10175910 | TAGTACAGTCACAGC[A/G]TTGCACAGCCACCAC | 10277 |
rs115385107 | snp | A/G | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093789 | AACCTCCGCCTCCCA[A/G]GTTAATGCGATTCTC | 10277 |
rs115385362 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UBE4B | GRCh38.p7 | 1:10124481 | GTGTGAACCACAGCG[C/T]CTGGCCCAGACCTGT | 10277 |
rs115401210 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10101366 | TTACCCTTATTCATG[A/G]AAGTGTAACTCAGTC | 10277 |
rs115486679 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UBE4B | GRCh38.p7 | 1:10123054 | TGTTTATCTTAGGTG[A/G]TGATCTTACTGACTA | 10277 |
rs115486804 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10157210 | ATTAATAGTAGAGGC[A/G]GGGTTTTGCTATGTT | 10277 |
rs115566512 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBE4B | GRCh38.p7 | 1:10065830 | ATTTATGTATAATTT[A/G]CACTAATAATAATGT | 10277 |
rs115576431 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBE4B | GRCh38.p7 | 1:10113783 | AACATAAGATGCTTT[C/T]CGGCCGGACGCAGTG | 10277 |
rs115620463 | snp | C/G | 0.100231 | 0.200173 | intron-variant | UBE4B | GRCh38.p7 | 1:10076213 | GATTGAGAGATTTTT[C/G]TTCCAGACTCAAAAA | 10277 |
rs115624399 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | UBE4B | GRCh38.p7 | 1:10167830 | TCTCGACCTCGTGAT[G/T]CGCCCACCTTGGCTT | 10277 |
rs115625504 | snp | C/T | 0.079617 | 0.182947 | intron-variant | UBE4B | GRCh38.p7 | 1:10042633 | GCCTGGGCGACAGAG[C/T]GAGACTGTGTCTCAA | 10277 |
rs115627613 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10136785 | GTAGCCAGGTGTGGT[A/G]GCACACGCCTGTAAT | 10277 |
rs115629793 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | UBE4B | GRCh38.p7 | 1:10144810 | CTGGTTGTAAGATAT[A/T]CTCTGATTTTAAAGA | 10277 |
rs115641062 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10078312 | CCGTGCCTGGCTGAT[C/T]ATGCTACTTTTATAT | 10277 |
rs115641525 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10144297 | TAGGCAAAGTAACCT[C/T]GAATTTTCATGAGAG | 10277 |
rs115645382 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10039734 | CGTGAGCCACTGCAC[A/G]TGGCTGAGTTTGAAC | 10277 |
rs115657148 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE4B | GRCh38.p7 | 1:10068887 | CCAGAACGCTGCCCC[C/T]TGCATGGCTCTTCCT | 10277 |
rs115659120 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10159206 | GTCATTTAAAGTATC[A/G]TTCTTTGTGGTAAGG | 10277 |
rs115751265 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10079599 | ATGAAAGACTTAGCA[A/G]CTAGTCAAACTGCTT | 10277 |
rs115772503 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10110072 | TCATTGATCTTCCCA[A/G]AATTTTTTTACTCTG | 10277 |
rs115776359 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170730 | ATTTATGGGGAAAAA[A/T]GTTTATGAAATACTG | 10277 |
rs115779448 | snp | A/G | 0.0399052 | 0.1355 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094873 | TTGGCTCACTGCAAC[A/G]TCTTCCTCCCAGATT | 10277 |
rs115835954 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBE4B | GRCh38.p7 | 1:10154200 | ATGAGCCAAGATCGC[A/G]CTACTGCACTTCAGC | 10277 |
rs115897115 | snp | A/C | 0.0280515 | 0.115694 | intron-variant | UBE4B | GRCh38.p7 | 1:10148262 | TAGCTCTGTTGTTTC[A/C]GTTTGAGTTGCACAA | 10277 |
rs115902661 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | UBE4B | GRCh38.p7 | 1:10142186 | CCTCAAATACTAATT[G/T]TATCTTCACCATGCA | 10277 |
rs115934984 | snp | C/T | 0.0452528 | 0.143452 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032681 | TTCTGGTGGATCTTC[C/T]CCGACGCGAGTCTGG | 10277 |
rs115953956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087340 | ATGTACAGAAAAGTT[A/G]TGAAGATAGTATACA | 10277 |
rs115983170 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10155125 | TTTGTGTATTTGTGT[G/T]TACACAACAGAACTG | 10277 |
rs115992551 | snp | A/T | 0.0618563 | 0.164627 | intron-variant | UBE4B | GRCh38.p7 | 1:10174067 | TGAAACAAACACACA[A/T]GTGCCAGTGACACAT | 10277 |
rs116019519 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10110583 | TTACCCCATGGTAAA[G/T]GTACCGCAGAAGTTA | 10277 |
rs116021221 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10151679 | CTACCTGTGTGTATA[A/G]CCTACTAACCTGTGG | 10277 |
rs116030309 | snp | C/T | 0.000537544 | 0.0163855 | intron-variant | UBE4B | GRCh38.p7 | 1:10103118 | AGCTCAGCAGTCTTA[C/T]TGCAGAGTACTCGAC | 10277 |
rs116066815 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | UBE4B | GRCh38.p7 | 1:10087587 | TTGTCTGGTGTTTTG[C/T]TCATGATAAGACTGG | 10277 |
rs116069382 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10051282 | TGGAATACCATCTCG[A/T]AGCACTGTTCTTCAG | 10277 |
rs116075454 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE4B | GRCh38.p7 | 1:10136208 | CTGGGAATGGTGGCT[C/T]ACATCCATAATCCCA | 10277 |
rs116076707 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBE4B | GRCh38.p7 | 1:10173915 | GGTGACCAACCACAC[A/G]TTGCATTGCCTGGTC | 10277 |
rs116102434 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10038504 | TTACAAGTCAGGAAA[C/T]TGGGATTCAGGTTAA | 10277 |
rs116148775 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10111683 | AATGCAAGGCCAGGC[A/G]CGGTGGCTCACACCT | 10277 |
rs116179719 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | UBE4B | GRCh38.p7 | 1:10131377 | AGCTACCTAGCTACT[C/T]GGGAGGCTGAGGCAC | 10277 |
rs116272747 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10048942 | AATCACTACTTTCTT[C/T]ATTCATTCAACACTC | 10277 |
rs116287312 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10037546 | TCGTATCTCAAGGTG[A/G]TGCTGTGAGTAGGTG | 10277 |
rs116338236 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | UBE4B | GRCh38.p7 | 1:10104950 | ACAGTAAATCAACTG[A/G]GAGCTGCAAAGAATA | 10277 |
rs116341217 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | UBE4B | GRCh38.p7 | 1:10065685 | TGGAGCAGGGCTACA[C/T]TTTCATCTGAATGTT | 10277 |
rs116352448 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10129809 | GCATGCATTACCATG[C/T]GAGGCTAATTTTTTT | 10277 |
rs116364469 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095073 | CATGAGCCACTGCAT[C/T]GGCCTGGTTTATTAA | 10277 |
rs116411164 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBE4B | GRCh38.p7 | 1:10120591 | CCTGTAATCCTATCA[C/T]TTTGAGAGGCCAAGG | 10277 |
rs116416434 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10038781 | TCCCAATTTTTTTTT[A/T]AAATGCCTGTCGCGT | 10277 |
rs116458741 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10115552 | GCTGGGATTACAGGC[A/T]TGAGCCACCGCGTTT | 10277 |
rs116460190 | snp | A/G | 0.00163805 | 0.0285717 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10132404 | GCATAGTATTTTGTT[A/G]AATGGCGAAACCCGT | 10277 |
rs116495892 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE4B | GRCh38.p7 | 1:10048088 | TCCTGACTTCAAACA[A/G]TCCTCCTTCCTTGGC | 10277 |
rs116508686 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10121154 | TGGATCACCTGAGGT[C/T]AGGAGTTTGGGACCA | 10277 |
rs116564452 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10063677 | TGGGAGGCCAAGTCA[G/T]GCGGATCACTTGAGG | 10277 |
rs116568784 | snp | A/T | 0.031825 | 0.122064 | intron-variant | UBE4B | GRCh38.p7 | 1:10141707 | TGGAAGCGAAGAGGG[A/T]TGATGGGTTAGAACC | 10277 |
rs116581180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036846 | TTAAAACAGGCAAGG[C/T]GGTGATCTTTTAATC | 10277 |
rs116586213 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10165530 | TTATCACTCAGAGCC[A/G]AATCCTGTGGTGAGA | 10277 |
rs116601933 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10127248 | AAAAAAGGCAAAGCT[A/G]TACATACTAAGAAAA | 10277 |
rs116659592 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10151814 | CAGATGATTGGCACC[A/G]AGACCCAGGGTATCA | 10277 |
rs116661119 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | UBE4B | GRCh38.p7 | 1:10061341 | CCCACTACAACCTCC[A/G]TTTCCTGGGTTTAAG | 10277 |
rs116672048 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | UBE4B | GRCh38.p7 | 1:10044684 | CCGCTTGGGCTCAAG[A/C]GATCCTCCCACCTCA | 10277 |
rs116689342 | snp | A/G | 0.00715027 | 0.0593634 | intron-variant | UBE4B | GRCh38.p7 | 1:10033719 | TTGGGGGACACCTTG[A/G]GGGATTAGTTGGCAA | 10277 |
rs116692329 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10139292 | GCTACTTGGGAGGCT[A/G]TAGCAGGAGAGTCGC | 10277 |
rs116708561 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10153454 | ATGATCTTGCTGCTG[C/T]GTTCCAGCCTGTGAA | 10277 |
rs116724197 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE4B | GRCh38.p7 | 1:10108382 | GCCTTTGAAATGACC[A/G]CAGAGGCTGAAACAT | 10277 |
rs116782657 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | UBE4B | GRCh38.p7 | 1:10037970 | GGTTGGCTGGGATTC[A/C]GGGTGTGGTCAAGAT | 10277 |
rs116792953 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10144215 | AGAGAAGAGCATTGC[G/T]AGCAGAGGGAACAGT | 10277 |
rs116800840 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | UBE4B | GRCh38.p7 | 1:10155969 | TGGGAGGTGGAGGTC[G/T]CAGTGAGCCAAGATC | 10277 |
rs116819138 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10158629 | AGATGCCACTAAATG[C/T]GGGCAGGATTTTTTA | 10277 |
rs116826516 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10084185 | TTGTCATGTGCCCAA[A/G]CCTAGCAAAGGCACA | 10277 |
rs116875717 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | UBE4B | GRCh38.p7 | 1:10033752 | CGTTAGCGCTTTGGA[C/G]AGGGATGGTATTGCG | 10277 |
rs117325767 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10171892 | TCTCAAAATAAATAA[A/G]TAAGTAAGTAAGTAA | 10277 |
rs117377626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142359 | TTAAAACAACACATA[C/T]TACAGTTCTGAAGGT | 10277 |
rs117537003 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | UBE4B | GRCh38.p7 | 1:10055395 | TCATAGCTCACTGTA[G/T]CCTTGAACTCCTGGG | 10277 |
rs117583935 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE4B | GRCh38.p7 | 1:10149658 | CTCAATTGTAAAATT[A/G]GAGAATGCTTACCAA | 10277 |
rs117663899 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10117070 | GTCAGTCCCTTATAA[C/G]TTTTCCCCCAAAGAG | 10277 |
rs117794506 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBE4B | GRCh38.p7 | 1:10162925 | GGTCCTATCCAAATA[C/T]TCCCTCAGGTTTGTC | 10277 |
rs117863162 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | UBE4B | GRCh38.p7 | 1:10152156 | CTGTAGTCCCAGGGC[A/G]GTTGAGGGAGGAGAA | 10277 |
rs118084717 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10059887 | AGCCAAGGGAAGGCT[G/T]CTTCTACCCAGGAGA | 10277 |
rs118126602 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | UBE4B | GRCh38.p7 | 1:10137874 | ATGAGAGAAACTGAA[C/T]CATATTTATATCTCT | 10277 |
rs137880656 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10085827 | CAGAGTCTCGCCCTG[C/T]TCCCCAGGCTGGAGT | 10277 |
rs137928298 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10053906 | GCCCAGGCTGGTCTT[-/G]GAATTCCTGGGTTCA | 10277 |
rs137951078 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | UBE4B | GRCh38.p7 | 1:10131856 | GACTTGGGAGGCTGA[G/T]GCAGGAGAATCGCTT | 10277 |
rs137960150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045548 | GTCTACAGTCTGACA[C/T]ATTTGATGAAATATG | 10277 |
rs137970595 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10126127 | AACAAAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 10277 |
rs137984053 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10166837 | GGCTGAGGCAGGAGA[A/T]TGGCTCGAACCCGGG | 10277 |
rs138009294 | in-del | -/TT | 0.397452 | 0.201886 | intron-variant | UBE4B | GRCh38.p7 | 1:10092223 | AGTGAGACCCATCTC[-/TT]TTGTTTTGTTTTGTT | 10277 |
rs138030773 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10042038 | CTCCTGAATTCAAGC[A/G]ATTCTCCTGGGTCAG | 10277 |
rs138056371 | snp | A/G | 0.0128029 | 0.078978 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135127 | GGATTACTCTTCCCA[A/G]TGATGAGACGCGTGT | 10277 |
rs138083563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051079 | TGGCATTATCATAGC[C/T]CACTGCAGCCTCAAA | 10277 |
rs138107259 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10064622 | CACTCTCTATCACCT[C/T]GTCTCTTTGTCACTT | 10277 |
rs138208446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075041 | TCCCAGGTTTCCATC[C/T]CAATAAATGACAATT | 10277 |
rs138229380 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBE4B | GRCh38.p7 | 1:10111231 | ACACACACACACCAC[A/G]CGCTACACACACACC | 10277 |
rs138261561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10156861 | ACAAAAAAATGTGTT[C/T]TTTGGAAAATACAGA | 10277 |
rs138345401 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10035724 | GATAGTTTTTTTATT[A/T]TTTTTTATTTTTTAT | 10277 |
rs138350900 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10065423 | GAAGGAAGAGGAGAC[C/T]GCTGTACTTCACTGT | 10277 |
rs138381889 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | UBE4B | GRCh38.p7 | 1:10047187 | TCTGTGTATTAGTTA[A/G]GATATTGATTTGACT | 10277 |
rs138396092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10140964 | AGTTGGTTGCATAAT[A/G]TGAACCTCTCCCAAC | 10277 |
rs138407167 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10062370 | CAGGCTGGAGTGCCA[C/T]GGCACGATCCTGGCT | 10277 |
rs138412948 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10165326 | GCCTCTAAGCTCTGT[C/G]TTAAAATATATCCAT | 10277 |
rs138441079 | in-del | -/A | 0.0275645 | 0.114116 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033382 | GAAGCAGAGGGTAAT[-/A]AAGTGGCGCCTTAAG | 10277 |
rs138455167 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10121777 | TCCCATAGTGTCTCA[C/T]TAAAAAGACCAAAAA | 10277 |
rs138456258 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10071371 | AGGATCACTTGGGGC[C/T]AGGAGGTTGAGACCA | 10277 |
rs138485457 | in-del | -/AAAAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060603 | TTACCAAAACAAAAC[-/AAAAG]AAAATAAAAACCTTT | 10277 |
rs138490506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10117815 | ATAGAGACAGAGCCA[A/G]GGTTTGAACCTAGAT | 10277 |
rs138527945 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10096210 | ATTAGTGAAATTTAA[A/C]AGTTTGGAATATTTC | 10277 |
rs138611970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10097893 | TATTTTTTTTGGAGA[C/T]GGAGTCTCACTCTGT | 10277 |
rs138615805 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10172241 | TTCTAGTCATCCCAT[A/G]AAGGGCTGGCCCCCT | 10277 |
rs138618218 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10061446 | TTTTTTATTAGAGAC[A/G]GGGTTTCACCATCTT | 10277 |
rs138636534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126468 | TTGAGTAGAGCAACG[A/G]CTCCTGGAGAGTTCT | 10277 |
rs138638392 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119519 | CCTTTTCAGATGTGC[A/G]GCCAGCCAGCAGTCA | 10277 |
rs138653797 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135460 | AATACAAAAATTAGC[C/T]GGGCATGGTGGCACA | 10277 |
rs138657275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132201 | GCTCATTACTTTGAC[A/G]TAGTTGGATGTGGAT | 10277 |
rs138666636 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074039 | AAACTCCCAGGCTCA[A/G]ATGATCCGTCTGCTT | 10277 |
rs138691927 | in-del | -/AAAAAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125128 | GAAATTGTGTCTGGA[-/AAAAAG]AAAAAGAAAAAGAAA | 10277 |
rs138700382 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10085282 | CCTTTGTTCCCTTCT[C/G]CTTCTCCTAGTGACA | 10277 |
rs138721078 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10116844 | GAGACTAGAACCCAC[A/G]TCTGGTTACTCCTAG | 10277 |
rs138734215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10138486 | CGATCCGACTGCCTC[C/T]GCCTCCCAAAGTGCT | 10277 |
rs138736106 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10092659 | ATGGTTAAACCCCAT[C/G]TCTACTAAAAGTACA | 10277 |
rs138740567 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10080187 | AGCACTTTGGGAGGC[C/T]GAGATGGAGGGATCA | 10277 |
rs138771768 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10134634 | TGGAATGACAGTGGT[G/T]ATGAGATATATGTCT | 10277 |
rs138806933 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10034426 | TTCTTAAAGGAGTTA[C/T]ACAGATCTACTTCTT | 10277 |
rs138819519 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10070222 | GAGGTTGCAGTGAGC[C/T]GAGATGGTGCCATTG | 10277 |
rs138866959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143346 | GTCAGAGGTTGCAGT[A/G]AGCCAGATGATGCCA | 10277 |
rs138879358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122624 | AAATGCAGATATGTA[A/G]TGCTTAAAAATAAAG | 10277 |
rs138900358 | snp | C/T | 0.000659794 | 0.0181511 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10145006 | GGCAACTAGACACCG[C/T]GAAATGCTGAAGCGC | 10277 |
rs138912462 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10160998 | TGGTCCTTGAATTCC[A/G]TAGTGCCTGACTTGT | 10277 |
rs138954558 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10148832 | GTAATCTCAGCTATT[C/T]GGGAGGCTGAGACAT | 10277 |
rs139019080 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10144224 | CATTGCGAGCAGAGG[C/G]AACAGTTGTAAAGGA | 10277 |
rs139022938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075423 | AGCCTCCTAACTGGT[C/G]ATCTCATGCCCACCC | 10277 |
rs139028862 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10152531 | GGCCAGGTGCGGTGG[C/T]TCATACCTGTAATCC | 10277 |
rs139088006 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10176069 | ACCTATTCACCTCTC[C/T]GGGATATTTCATATA | 10277 |
rs139095547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10149796 | AGAATTACAATTTCA[A/G]TCCCTTGGCACCATG | 10277 |
rs139108939 | snp | C/T | 0.000875244 | 0.0209011 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179528 | CACGGACCCCTTCAA[C/T]CGGCAGACGCTGACA | 10277 |
rs139159603 | snp | A/C | 3.2981e-05 | 0.00406071 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10102963 | GAGCCTTCCTCGGGC[A/C]CTGAAGTGTCTGAAG | 10277 |
rs139160510 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10102357 | ATCCTCTGTCACATA[A/T]TTTTCCTTGGTGACT | 10277 |
rs139164134 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10146672 | AAAGGGCCTCCCTGT[C/T]GCCACCCTCTCCTCA | 10277 |
rs139201516 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10077381 | GGATTAGGGACCACC[A/G]TAATTGAGTATGAGC | 10277 |
rs139245520 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10088046 | CTCTTTCAAGTTGGA[A/T]CCTTGGTCCATTTGA | 10277 |
rs139275899 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBE4B | GRCh38.p7 | 1:10102706 | GTGAGCCACCACGCC[C/T]GGCCATCTTTGCTCT | 10277 |
rs139279718 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10133293 | TTGTGATTTCTGATC[A/G]TGGTTCCACCGTTTA | 10277 |
rs139285315 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10093060 | ATACACTGGAGCTAT[A/C]TTGCTACAGTATTAT | 10277 |
rs139332035 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10162408 | TCGATCTCCTGACCT[C/T]GTGATCCGCCTTCCT | 10277 |
rs139350481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086384 | AAGTGTTCAGTGACT[A/G]TTAAATATGCACTGT | 10277 |
rs139384893 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10044731 | GGACCATAGGCGCAC[A/G]CCATCATGCCCGGCT | 10277 |
rs139385554 | snp | C/T | 3.33111e-05 | 0.00408099 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179447 | CCTCATGACAGACCC[C/T]GTGCGGCTGCCCTCT | 10277 |
rs139412405 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10144554 | GCCTGCCCAACATAG[C/T]GAAACCTCATCTCTA | 10277 |
rs139427057 | snp | A/C | 1.6552e-05 | 0.00287676 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135086 | AGAAACAGTTGATCC[A/C]ACGTATATTTTTCAC | 10277 |
rs139428467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10047928 | CCAGGCTAGAGTACA[A/G]TGCAGCCTCTAACTC | 10277 |
rs139431848 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10037533 | CATGTGTTGTTTTTC[A/G]TATCTCAAGGTGGTG | 10277 |
rs139439907 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10119171 | CAGGCGTGAGCCACC[A/G]TGCCCGGCCCAGGCT | 10277 |
rs139444428 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10154185 | GAGGCAGAGGTTGCA[A/G]TGAGCCAAGATCGCG | 10277 |
rs139482662 | snp | A/G | 0.031825 | 0.122064 | intron-variant | UBE4B | GRCh38.p7 | 1:10162600 | GGCGTGAGTCACCGC[A/G]CCCAGACTTTTTTTT | 10277 |
rs139498869 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031038 | TGTATTGCTCCACTG[A/C]TGTGAAATGTCCAGA | 10277 |
rs139503004 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10114635 | TTGTGAGGCTGAGGC[A/C]GATGGATCATTTGAG | 10277 |
rs139505257 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10157160 | GCTGGAATTATGGGC[A/G]CACACCACCATGCCC | 10277 |
rs139515866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113563 | GTGAGTGCACGGTTT[A/G]TGAAAATATTTCAAG | 10277 |
rs139552681 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | UBE4B | GRCh38.p7 | 1:10157715 | CCCCGAGGCAGAGGT[C/T]GCAGTGAGCTGAGAT | 10277 |
rs139557744 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10051475 | CATAAATAGTGGTAT[C/T]TTACTAGTTAAGGTA | 10277 |
rs139578862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048460 | TTACCTAGAGAGTGA[A/G]CATAAATGCGGAAGA | 10277 |
rs139629758 | snp | C/G/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10167237 | CTGACGTCAGGAGTT[C/G/T]GAGACCAGCCTGACC | 10277 |