SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1563 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495905 | TTACAGAATACCTAT[C/T]GAGATATTACACCTA | 115426 |
rs370132 | snp | A/G | 0.49928 | 0.018956 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456221 | gccagttagaatggc[A/G]atcattaaaaagtca | 115426 |
rs370818 | snp | A/C | 0.365232 | 0.22186 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456266 | cattagagaaacgca[A/C]atcaaaaccacactg | 115426 |
rs375835 | snp | A/T | 0.49975 | 0.0111793 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456230 | ccatatcacgccagt[A/T]agaatggcgatcatt | 115426 |
rs380674 | snp | A/T | 0.435837 | 0.167226 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438131 | GACCTGGATTATGAT[A/T]GTTCCCATATTGTAA | 115426 |
rs386632 | snp | C/T | 0.378765 | 0.214288 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456155 | CTCTCTAGAAACATT[C/T]TAAAAAGAAAAAAGC | 115426 |
rs394137 | snp | A/G | 0.435119 | 0.16802 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440619 | ACACACGCAACTTCT[A/G]TTGAGCTAAACCGTA | 115426 |
rs401733 | snp | C/T | 0.497641 | 0.0342639 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455048 | CCTACCTTTGATAGA[C/T]TGAGCTTTTTAAGAG | 115426 |
rs407351 | snp | A/T | 0.348794 | 0.229651 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451638 | GGCGCCCGCCACCAC[A/T]CCCGGCTAATTTTTA | 115426 |
rs414107 | snp | C/T | 0.386123 | 0.209692 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439294 | GGTTCAAACGATTCT[C/T]CTGTCTCAGCCTCCT | 115426 |
rs424119 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439943 | CATTAAGTGGTTAAT[A/G]TAAAAGAAAAAAGGG | 115426 |
rs427077 | snp | A/G | 0.347473 | 0.230215 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451579 | CCCCCCGGGGTTCAC[A/G]CCATTCTCCTGCCTC | 115426 |
rs452135 | snp | A/G | 0.38555 | 0.210062 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441207 | aacatggcaaaaccc[A/G]gtctctacaaaaaaa | 115426 |
rs503315 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439075 | TACAAACACTAAGTT[C/T]ATGAAAAACAGGTTA | 115426 |
rs504698 | snp | A/G | 0.4444 | 0.15719 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463435 | AACGTTAGGAACACA[A/G]TAGCTAAAAAGGAAC | 115426 |
rs513526 | snp | C/T | 0.498964 | 0.02274 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459604 | tcagctcactgccac[C/T]tccacctcctgggtt | 115426 |
rs519674 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450623 | TAATTCCCTAGAATC[C/T]TTCAAAGGTTGACCG | 115426 |
rs524888 | snp | C/T | 0.498059 | 0.0310896 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459274 | GAAAATGGAGACTAT[C/T]GGAATATGCCAGGTT | 115426 |
rs530722 | snp | C/T | 0.442113 | 0.159977 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462813 | TCCCAGCTACATGGG[C/T]GGCTGAGGCAGAGGA | 115426 |
rs531571 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446690 | aaccccgtctctata[C/G]gaaaatttgcttggt | 115426 |
rs535725 | snp | C/T | 0.4973 | 0.0366419 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462346 | AAAAAAAAAATGATG[C/T]GAGGTGTTGAAAACT | 115426 |
rs541378 | snp | A/G | 0.499784 | 0.0103811 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465465 | GTTCTTTTATGGTCA[A/G]TTCGGTTTCTGTAAT | 115426 |
rs553048 | snp | C/G | 0.0547245 | 0.156101 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443567 | ATAACTTAAAAATTT[C/G]TGTTTATCTCTCTAG | 115426 |
rs559438 | snp | A/C | 0.0528381 | 0.153711 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455445 | tttccagcttcatcc[A/C]tgtccctacaaagga | 115426 |
rs560059 | snp | A/G | 0.406296 | 0.19512 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447196 | gcccagccAGCACAC[A/G]TACCTTTTAACCTAA | 115426 |
rs563779 | snp | A/C | 0.495291 | 0.0482933 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447591 | TAAGAAGAAATGAAA[A/C]TAAAGGTAAATAAAG | 115426 |
rs568386 | snp | C/T | 0.499234 | 0.0195537 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455777 | AGCTGGTCTCAGACT[C/T]CAGGGCTGAAGCAAT | 115426 |
rs569866 | snp | A/C | 0.44755 | 0.153212 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466285 | GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 115426 |
rs578124 | snp | C/T | 0.396727 | 0.202413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458054 | aactattccaaacaa[C/T]aggaaaagagggact | 115426 |
rs1044642 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507006 | CTAAATTTTATATTC[A/C]CTATATTCCCTAAAG | 115426 |
rs1156747 | snp | A/G | 0.424814 | 0.178718 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423233 | AAGTACCAGGCTTGG[A/G]TGGCTGAATTGTTTT | 115426 |
rs1156867 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417950 | AAAAATGTTCTTTCA[A/G]TTTCCAGCAGTTTTA | 115426 |
rs1156868 | snp | A/T | 0.084364 | 0.187256 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417972 | GCAGTTTTATCACTT[A/T]AACTGCTATCTTCAT | 115426 |
rs1156869 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418000 | CATTTTTGGAAATAT[C/G]CTACTAGTTAATTTG | 115426 |
rs1156870 | snp | C/T | 0.13446 | 0.221699 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418060 | TATCTTTAAGCACTT[C/T]CATTTAAAAATAGTC | 115426 |
rs1270597 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456954 | catgatgccaccagc[C/T]ttgttctttttgctt | 115426 |
rs1272800 | snp | A/G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456975 | ctttttgcttaggat[A/G/T]gtcttggctatacgg | 115426 |
rs1272801 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6457078 | atggggacagcattg[A/G]atctataaattactt | 115426 |
rs1381035 | snp | A/T | 0.41408 | 0.188621 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429909 | TAGTAAAACCATCAA[A/T]TATTTGCTGTTGGTA | 115426 |
rs1381036 | snp | A/G | 0.420892 | 0.182472 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429924 | ATATTTGCTGTTGGT[A/G]TTTTCTTTTTTTAAT | 115426 |
rs1381037 | snp | A/G | 0.422 | 0.181428 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430156 | GCTGGGATTACAGGT[A/G]CATGCCACCATGCCC | 115426 |
rs1824537 | snp | A/G | 0.421526 | 0.181876 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430182 | TGCCCGGCTAATTTT[A/G]TACTTTTAGTAGAGA | 115426 |
rs1870696 | snp | G/T | 0.228253 | 0.249052 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452927 | TATTATGCGCTCAAA[G/T]GTTACCTAATATTTT | 115426 |
rs1903419 | snp | A/G | 0.443732 | 0.158012 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433304 | CATTTTGTGTCTTAC[A/G]CCCTGTTCATTTTTA | 115426 |
rs1929929 | snp | A/G | 0.284209 | 0.247648 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499994 | CAAGAGTGAGACCCC[A/G]TCTCAACAACAACAA | 115426 |
rs2065074 | snp | A/G | 0.445855 | 0.155373 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420225 | TACTAGAAATACAAA[A/G]TATTAGCTGGGCGTG | 115426 |
rs2065075 | snp | A/T | 0.441432 | 0.160792 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418041 | TGCTTAAAGATAATT[A/T]AAAAAAACTAACAGT | 115426 |
rs2145991 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451977 | AAAGTGTATTGtgta[C/T]atatgcatttgtata | 115426 |
rs2169283 | snp | A/C | 0.424348 | 0.179172 | intron-variant | UHRF2 | GRCh38.p7 | 9:6413919 | TGTATTTGGTAGGAC[A/C]GCGGCCGTAGGCACT | 115426 |
rs2169286 | snp | A/C | 0.416871 | 0.186156 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425256 | TATGAACTCAtgatc[A/C]aattgttccactttt | 115426 |
rs2295844 | snp | C/G | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460458 | TAAGGACACTTCAAC[C/G]TATTTTACTCTTTCT | 115426 |
rs2297445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496863 | GGGGAAGGGAGAACG[C/T]TGGAAAACTAAAGCA | 115426 |
rs2381444 | snp | C/T | 0.448195 | 0.152377 | intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6413895 | CCGGAGCGCAAATAT[C/T]TCGCCGTTTGTATTT | 115426 |
rs2381445 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446413 | ctcccaaagtgctgg[A/G]tttacaggcgtgagc | 115426 |
rs2381447 | snp | A/G | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460839 | ACTGAATTGATCAAG[A/G]AATGTATTTTTAGGT | 115426 |
rs2777945 | snp | C/T | 0.499913 | 0.00658888 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457102 | ttgtgaaaatgccca[C/T]actgcccaaagtaat | 115426 |
rs3070894 | in-del | -/AAG | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460836 | TTAACTGAATTGATC[-/AAG]GAATGTATTTTTAGG | 115426 |
rs3739654 | snp | A/G | 0.33514 | 0.235254 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468447 | TGCACCAGAGAATCA[A/G]AGAGAACCAACTGCG | 115426 |
rs4380997 | snp | A/G | 0.429538 | 0.173972 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470639 | TTAAAATATACATAG[A/G]AAAAAAATGCGTGAC | 115426 |
rs4384035 | snp | A/G | 0.318656 | 0.240388 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457938 | aggatttttgcatca[A/G]tgttcatagggatat | 115426 |
rs4463484 | snp | C/T | 0.422315 | 0.181128 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480382 | CATTTATCCCCAGCA[C/T]GAAAATAGTGCCTTG | 115426 |
rs4556138 | snp | C/T | 0.447938 | 0.152711 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469486 | ttgcgccactgcact[C/T]cagcctggcgacaga | 115426 |
rs4740844 | snp | C/T | 0.434253 | 0.168969 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424566 | agatttgtagcaaaa[C/T]tgaagatagtagaga | 115426 |
rs4740845 | snp | A/G | 0.451234 | 0.14834 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424634 | AGATCTTAAGTTAGT[A/G]TGGTGTATTTGTTGA | 115426 |
rs4740846 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469793 | ATATATATGTATATA[C/T]GTGTATATATATATT | 115426 |
rs4742198 | snp | A/C | 0.0547245 | 0.156101 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419653 | CAAGCACTGATTAAA[A/C]ATAAAACTTGAGAAA | 115426 |
rs4742199 | snp | C/T | 0.452103 | 0.147154 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419853 | taaagtgatctccca[C/T]ctcagcctcctgagt | 115426 |
rs4742200 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430254 | acctcaggtgatcca[C/T]ccaccctggccccct | 115426 |
rs4742201 | snp | C/T | 0.421684 | 0.181726 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430502 | ggagagactgccctt[C/T]ttcctagagctagct | 115426 |
rs4742202 | snp | A/G | 0.421526 | 0.181876 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430598 | cgagtccatgcactt[A/G]actacctcccttatc | 115426 |
rs4742203 | snp | A/G | 0.079617 | 0.182947 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435768 | gcttggtaccacacc[A/G]ggctaattcttctat | 115426 |
rs4742204 | snp | C/G | 0.439918 | 0.162576 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435819 | TCACTATGTTGGCCA[C/G]GGTGGTCTCGAACTC | 115426 |
rs4742205 | snp | C/G | 0.32955 | 0.237006 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448912 | TGGATTTTCAATTGC[C/G]TAGCATTTGTGTTTA | 115426 |
rs5896148 | in-del | -/G | 0.0607341 | 0.163335 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412951 | AACGGCAACCGATGT[-/G]GGTAGCCGCGCAATC | 115426 |
rs5896151 | in-del | -/GGA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460838 | AACTGAATTGATCAA[-/GGA]ATGTATTTTTAGGTA | 115426 |
rs5896152 | in-del | -/A | 0.495056 | 0.049474 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462293 | TACTTTCTGGCTCTT[-/A]CGTGGGAAAAGTTTG | 115426 |
rs6477085 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458548 | ctagcttttgaatgt[A/G]tttgctcttgcttct | 115426 |
rs6477086 | snp | A/G | 0.44755 | 0.153212 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470232 | aaaaaatttagccat[A/G]cgtggtagtgcacac | 115426 |
rs6477087 | snp | A/C | 0.43978 | 0.162738 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472714 | atattataactaaaa[A/C]gtagaaggGAAATAT | 115426 |
rs7020390 | snp | A/G | 0.496245 | 0.0431677 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470921 | GCAGAAACAAACACA[A/G]CTGTATCAGCCTTTA | 115426 |
rs7021472 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489735 | gggtttttgtttttt[G/T]TTTTTTTTTTTACCA | 115426 |
rs7027302 | snp | G/T | 0.379746 | 0.213696 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458236 | gtttcgtcttgggag[G/T]gtgtatgtgtccagg | 115426 |
rs7027361 | snp | A/G | 0.488545 | 0.074807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451088 | AAATCACAGTTCCTA[A/G]TGATATCACTGATTT | 115426 |
rs7028825 | snp | C/T | 0.292523 | 0.246357 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428575 | ttttttttttttgaa[C/T]gatctcattctgtca | 115426 |
rs7029498 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446673 | cctggccaacgtggt[A/G]aaaccccgtctctat | 115426 |
rs7029772 | snp | A/T | 0.437683 | 0.165152 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497589 | AAGGTTTTTTTTTTT[A/T]AAATGTAAGTGTATG | 115426 |
rs7030161 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446477 | gtagaagcagggttt[C/T]gccatgttgcccagg | 115426 |
rs7033570 | snp | A/G | 0.191461 | 0.24305 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440123 | TAAATTCACAAAACT[A/G]ACAGCAGTCTTGCAA | 115426 |
rs7033940 | snp | C/G | 0.343701 | 0.231776 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440419 | TCTATTAAACTGTCT[C/G]ACTCAAGAGCCCAAG | 115426 |
rs7034328 | snp | A/C | 0.227369 | 0.248974 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477350 | accaacatggagaaa[A/C]cccatctctactaaa | 115426 |
rs7037825 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444862 | ctgccccggcctccc[A/G]aagtgctgggattac | 115426 |
rs7041671 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6415361 | ATAAACCAGTAGGGT[A/T]GAGGAATAGACCTTT | 115426 |
rs7042490 | snp | A/G | 0.0396438 | 0.135094 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412271 | AAGGCGGGGTGGGGG[A/G]TGGGGGAAGCCCTGT | 115426 |
rs7043824 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427721 | GAAGTTATTTATTGC[C/T]CAATATCATTATTTT | 115426 |
rs7044749 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415241 | AGACTTTCAGTAAAC[C/T]AGGAAGCTCATTCCA | 115426 |
rs7467926 | snp | A/G | 0.365646 | 0.221644 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459221 | taaattttaaaaaaa[A/G]aaagaaagaaactgg | 115426 |
rs7847139 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452937 | GTAACATTTGAGCGC[A/G]TAATAGGTTCCCGAC | 115426 |
rs7848831 | snp | C/G | 0.444267 | 0.157354 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504049 | TTTTTTTTTTAAGAC[C/G]GAGTCTCGCTCTGTC | 115426 |
rs7850918 | snp | C/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477573 | TATGAGATTCATAGA[C/T]ATAAAAAATGTTTTA | 115426 |
rs7851003 | snp | C/T | 0.423881 | 0.179625 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469705 | acacgtatatacata[C/T]atatacacacatata | 115426 |
rs7851921 | snp | A/T | 0.0588605 | 0.161139 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411167 | TTTTGCCACCGAAAG[A/T]AATGGCAAAACCCCA | 115426 |
rs7852539 | snp | A/G | 0.442926 | 0.158996 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475319 | TGAGATTCCAAACTG[A/G]CTTTTAATTATTATT | 115426 |
rs7853059 | snp | A/G | 0.41023 | 0.191902 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436138 | TTCTTAACAAGTACG[A/G]GTTAGAAATCCTAGA | 115426 |
rs7853834 | snp | A/T | 0.408188 | 0.193589 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436779 | GCAACTTTTTTTGTC[A/T]GTTAGAATGAATGTT | 115426 |
rs7860627 | snp | A/G | 0.300926 | 0.244758 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473630 | CTAAATCTGATTGAG[A/G]CTGAGTCTTTAGCCC | 115426 |
rs7860966 | snp | A/G | 0.379942 | 0.213577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447394 | GGTACTTGCTCCTCA[A/G]TGAAAAATTGCTGTT | 115426 |
rs7861073 | snp | A/G | 0.380333 | 0.213338 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447439 | AAATATGCATACCTA[A/G]CTTTGAGAGTATAAA | 115426 |
rs7861559 | snp | C/T | 0.380138 | 0.213458 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447140 | atgatctgcccgctt[C/T]tgcctcccaaagtgc | 115426 |
rs7864027 | snp | A/C | 0.119978 | 0.213528 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504189 | CGCCGCCACGCCCAG[A/C]TAATTTTTTGTATTT | 115426 |
rs7864509 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483967 | gtgctgggattacag[A/G]cgtgagccactgcac | 115426 |
rs7869419 | snp | G/T | 0.11228 | 0.208646 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469964 | aaaTGCACAGTGGTA[G/T]ATCACAAACAAGAAT | 115426 |
rs7871134 | snp | C/G | 0.43598 | 0.167067 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437689 | GTGGTGCGATCTCAG[C/G]TCACTGCAACCTCCA | 115426 |
rs7872349 | snp | C/T | 0.242488 | 0.249887 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475893 | gtgttgggaacattc[C/T]aaatctattctttta | 115426 |
rs7872736 | snp | C/G/T | 0.0834134 | 0.189738 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485140 | TTAGTTTAatactct[C/G/T]tgtgttctcttatct | 115426 |
rs7873756 | snp | A/G | 0.442385 | 0.15965 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473409 | tcaccaactagttta[A/G]tgaggtcatttctct | 115426 |
rs7874061 | snp | A/T | 0.0584853 | 0.160693 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458010 | ttggtatcaggatga[A/T]gttggcctcataaaa | 115426 |
rs7874062 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458012 | ggtatcaggatgatg[C/T]tggcctcataaaatg | 115426 |
rs7874969 | snp | G/T | 0.0166151 | 0.0896185 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481601 | TTACTAGCTTTAATA[G/T]GGTATTGTGAAAATG | 115426 |
rs7875172 | snp | A/G | 0.093417 | 0.194889 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489209 | ctttttccactcagc[A/G]tgattctctggagat | 115426 |
rs7875793 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491980 | tcaagcaggccaact[A/G]ctttggcctcccaca | 115426 |
rs7876000 | snp | C/T | 0.308661 | 0.24302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476496 | ATGCAGCTGTACCTC[C/T]TCATTTAACGGATTT | 115426 |
rs10114592 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495358 | GAGAGACTTTAACAT[C/T]TGGTCAGTTTATACG | 115426 |
rs10115883 | snp | A/G | 0.424348 | 0.179172 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479626 | gggctttatattcct[A/G]tatgcagttggttag | 115426 |
rs10119350 | snp | C/T | 0.172028 | 0.23753 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496811 | TCCAGCAATTCACCT[C/T]ACACCCTTACCAAAG | 115426 |
rs10119962 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459692 | aaacaaaaaaCTTGA[G/T]gcctgacatggtggc | 115426 |
rs10121129 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444906 | caagtccagccTAGG[A/T]ATCTGCTTTTCAAAG | 115426 |
rs10122116 | snp | C/T | 0.424037 | 0.179474 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479215 | GTTTCCATTTCCTCT[C/T]CTATTCATACTTCAG | 115426 |
rs10124566 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448907 | GTGTTTGGATTTTCA[A/G]TTGCGTAGCATTTGT | 115426 |
rs10124572 | snp | A/T | 0.367091 | 0.220884 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448991 | CACCTTGCTTTAACC[A/T]TCATCAACTCATAGC | 115426 |
rs10125914 | snp | C/T | 0.424659 | 0.17887 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479464 | gagcaccccatccac[C/T]cccacccccaaccct | 115426 |
rs10283610 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414218 | TCCAGAACTTCTGGT[C/T]CCTCTCCCTCGCCGC | 115426 |
rs10283682 | snp | A/C | 0.0659589 | 0.169201 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412531 | GCTGGGAGCGCTGCA[A/C]GCCAGAGAGGGCGAT | 115426 |
rs10283728 | snp | C/T | 0.0681886 | 0.171594 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413017 | GCCAGGTGCAGGCGG[C/T]GGGGCAAGTAACGGC | 115426 |
rs10491838 | snp | A/G | 0.031825 | 0.122064 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438023 | CATGCCTTAAAAACA[A/G]TACCATCAGGACCTG | 115426 |
rs10733529 | snp | C/T | 0.45235 | 0.146814 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423110 | AGATGAAGTAAATTA[C/T]TCAAGATTATTCAAA | 115426 |
rs10739098 | snp | A/G | 0.429987 | 0.173507 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417677 | GAGTGGATAATCTGG[A/G]TTTAAAAAGCCTGTC | 115426 |
rs10739099 | snp | A/T | 0.441158 | 0.161117 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427481 | CACCTGAGGTCAGGC[A/T]TTTGCAACCATCCTG | 115426 |
rs10739100 | snp | A/C | 0.440746 | 0.161604 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427532 | TCTCTACTGAAAATA[A/C]AAAAATTAGCTGGCT | 115426 |
rs10739101 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427663 | GCACTCCTGCCTGGG[C/T]GACAGAGCAAGACCC | 115426 |
rs10739102 | snp | C/T | 0.441295 | 0.160954 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427684 | AGCAAGACCCCATCT[C/T]AAAAAAAAGAAATTT | 115426 |
rs10739103 | snp | A/C | 0.0513262 | 0.151752 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432156 | CTCTGATTGTTTGTC[A/C]TACCCAGCATGGTTG | 115426 |
rs10739104 | snp | G/T | 0.0558544 | 0.157504 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432353 | TTCTACCCTCTGTCA[G/T]TTTGTGGTTTGAAAC | 115426 |
rs10739105 | snp | A/G | 0.129664 | 0.219133 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490248 | TAGTATTTTATGTGG[A/G]GAAGATGATTACATT | 115426 |
rs10758784 | snp | C/G | 0.451359 | 0.148171 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415025 | TCCTTTTGATCACAA[C/G]TGAAAAAGCATGTAA | 115426 |
rs10758785 | snp | G/T | 0.430732 | 0.172731 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415230 | GGCAACAAAGTAGAC[G/T]TTCAGTAAACTAGGA | 115426 |
rs10758786 | snp | C/G | 0.442791 | 0.15916 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418822 | CCAAAACCTGGGTGG[C/G]TTAAAACAATAGAAA | 115426 |
rs10758787 | snp | C/T | 0.43221 | 0.171171 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418829 | CTGGGTGGCTTAAAA[C/T]AATAGAAATTTACTG | 115426 |
rs10758788 | snp | C/T | 0.415399 | 0.187465 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428051 | GGACTAAATAATGAC[C/T]GTTTAGAATGATGAT | 115426 |
rs10758789 | snp | G/T | 0.41408 | 0.188621 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431091 | ATACAGGCCTAAGTA[G/T]TTTTCCTCTGAACTG | 115426 |
rs10758790 | snp | A/T | 0.436123 | 0.166908 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431946 | GAAACTTACATTTTG[A/T]TTTGCTGCGACAGAG | 115426 |
rs10758791 | snp | C/T | 0.442404 | 0.166043 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435559 | AAAAGAAATCTCATA[C/T]TGATTATCAGTCACT | 115426 |
rs10758792 | snp | A/C | 0.442791 | 0.15916 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436089 | ACTAATCAAGTAATA[A/C]ATTAATATGTATGGA | 115426 |
rs10815431 | snp | C/G | 0.156319 | 0.231784 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411638 | GCCCACCTCGGCCTC[C/G]CAAAGCGCTGAGATT | 115426 |
rs10815432 | snp | C/G | 0.441705 | 0.160466 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416762 | TCGATCTCCTGACCT[C/G]GTGATCCGCCCGCCT | 115426 |
rs10815433 | snp | A/G | 0.491783 | 0.0635686 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423738 | ATCATGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 115426 |
rs10815434 | snp | A/T | 0.424193 | 0.179323 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424116 | CTAGATAATGCAATT[A/T]GGCAGGAGAACAAAA | 115426 |
rs10815435 | snp | C/T | 0.435837 | 0.167226 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437518 | GATTACAGGTATGAG[C/T]CACTGCACCTGGCCA | 115426 |
rs10815436 | snp | A/G | 0.35337 | 0.230364 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439587 | AGTAGATAGATATTT[A/G]TAAGTTTTTTTTCTG | 115426 |
rs10815437 | snp | C/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461365 | TCTCCCCCCCCTCCT[C/T]CTCTCCCCCTCCTCC | 115426 |
rs10975579 | snp | A/T | 0.424814 | 0.178718 | intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6413904 | AAATATCTCGCCGTT[A/T]GTATTTGGTAGGACA | 115426 |
rs10975580 | snp | A/G | 0.253264 | 0.249979 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414839 | CCTTCTCTCTTTAAA[A/G]TAATGTTATAGCACC | 115426 |
rs10975581 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416224 | gtgcgccaccactcc[C/T]ggcaaattttttgta | 115426 |
rs10975582 | snp | C/G | 0.442791 | 0.15916 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416635 | GCAAGCTCCGCCTTC[C/G]GGGTTCACGCCATTC | 115426 |
rs10975583 | snp | C/T | 0.44252 | 0.159487 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416844 | AATCTTTTGAGAATC[C/T]AGAGCTTTTCCTATT | 115426 |
rs10975584 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421445 | GATAACGGAGGCTTG[C/T]TCTGTCACCCAGGCT | 115426 |
rs10975585 | snp | C/T | 0.421051 | 0.182323 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424252 | AAAGTTAACATTGAG[C/T]TGCTGATAGCTCAAG | 115426 |
rs10975586 | snp | A/C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424795 | TTTTTTTTTTTTTTC[A/C/T]ATTACCGTGACCATT | 115426 |
rs10975587 | snp | A/G | 0.417683 | 0.185425 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429259 | CCACATTTTTTACCT[A/G]TGTATCTCTTGAGCA | 115426 |
rs10975588 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432484 | CAAGAACATAAGCTT[C/G]AAAGTCAAGATGTCT | 115426 |
rs10975589 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432816 | GAATTTCTCTTGGTT[A/G]TTGTCCTAAAAGGGC | 115426 |
rs10975592 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444297 | ATTTCCTCTAACTGT[C/G]TATGACTTGTAGGCT | 115426 |
rs10975593 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446281 | TCAGCCTCCCAGGTA[A/G]ATGGAATTACAGGCG | 115426 |
rs10975594 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448496 | TCTGTTTTTATTACC[A/G]TCCAAATAAATAACT | 115426 |
rs10975595 | snp | A/G | 0.393803 | 0.204501 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452555 | CCTAAAGATGGGGAA[A/G]TGTGTTGGGCCTAGT | 115426 |
rs10975596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456576 | CTTCTGTTGCCGTTG[C/T]TTTTGGTGTTTTGGA | 115426 |
rs10975599 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469435 | AGGCAGGAGAATCAC[A/C]TGAACCTGGGAGACA | 115426 |
rs10975600 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469694 | TGTATATATATACAC[A/G]TATATACATACATAT | 115426 |
rs10975601 | snp | C/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472616 | taaacatttaaaata[C/T]ttttacatttagaaa | 115426 |
rs10975602 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474909 | TTTTTGTAGATTTTT[A/T]AAATAAATTGTTACA | 115426 |
rs10975603 | snp | A/G | 0.309154 | 0.242901 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476213 | AAATGAAAGGATTCT[A/G]TTATTTTTTATGGCA | 115426 |
rs10975605 | snp | A/G | 0.4231 | 0.180378 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480005 | TGTTTGAAACCCTCT[A/G]ATGTCTTCCTATTTC | 115426 |
rs10975606 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480512 | ATATATCTCTACATT[C/T]GTATCAAGGTCTTTC | 115426 |
rs10975608 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485602 | AAGCTTCTAAAGTGC[C/T]TTTCCACCCCCGCCC | 115426 |
rs10975611 | snp | A/T | 0.313814 | 0.241719 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502279 | GCAGTGGTCACTGTT[A/T]TATTTAAACATGCTC | 115426 |
rs11787605 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482818 | agccaggatggtctc[C/G]atctcctaacctcgt | 115426 |
rs11790625 | snp | C/T | 0.312104 | 0.242163 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445304 | AGTCTTGCTCTGTCT[C/T]CCAGGCTGGAGTGCA | 115426 |
rs11791651 | snp | C/T | 0.428937 | 0.17459 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467989 | GACACCTCATCACAG[C/T]CTTTTTTTCTTACTT | 115426 |
rs11792128 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474530 | agccaacatggtgaa[A/C]ccctgtctctactaa | 115426 |
rs11792857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442636 | ggtgcacaccactgt[A/G]accagttaatttttg | 115426 |
rs11793232 | snp | C/T | 0.249603 | 0.25 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445998 | ttttttttttttttt[C/T]ttcctgtttttgaga | 115426 |
rs11795048 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446465 | ttttaatttttagta[A/G]aagcagggtttcgcc | 115426 |
rs11795228 | snp | C/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484789 | TTCACTTCtttcttt[C/T]ttttttttttttttt | 115426 |
rs11795355 | snp | C/T | 0.307423 | 0.243316 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479531 | actatgcttgttccc[C/T]agatgatctcgtcca | 115426 |
rs11998897 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429792 | GGACAAATTAAGTAA[C/T]TTGTTCATGGTTACA | 115426 |
rs11999359 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423654 | ttttttttttttaaa[A/G]aaaaGTCTCggccgg | 115426 |
rs12003279 | snp | A/C | 0.0792508 | 0.182605 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414400 | TACTTCTCGCCTTCT[A/C]ATACTCATGTCGTTC | 115426 |
rs12004123 | snp | G/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420887 | TTTTAGAGAAGCATT[G/T]CACTATTCTTTCTTT | 115426 |
rs12005560 | snp | G/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420877 | GTAAGATACATTTTA[G/T]AGAAGCATTTCACTA | 115426 |
rs12006537 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464698 | tcttcagtatcacct[C/G]tgtcatatcaagaat | 115426 |
rs12335918 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431004 | GCTACTCCTTTAGCT[A/G]ATTACTTCAGTTCTT | 115426 |
rs12337325 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6441205 | gcaacatggcaaaac[C/T]cagtctctacaaaaa | 115426 |
rs12339576 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433258 | GATTGCATGGGTTAG[C/T]TGTGGATCAGCCACT | 115426 |
rs12340729 | snp | C/G | 0 | 0 | splice-donor-variant | UHRF2 | GRCh38.p7 | 9:6486926 | TTTGCGGATGAAGTC[C/G]TAAGTCATTATACAA | 115426 |
rs12341324 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489736 | ggtttttgttttttt[G/T]tttttTTTTTACCAT | 115426 |
rs12342807 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6433420 | TAGATGGGTTCATTA[A/G]ACTCTTTTTTTTATT | 115426 |
rs12343008 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488128 | tgtgcctgtagtccc[A/G]gctacccaggaggat | 115426 |
rs12345895 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474246 | TTGTGTATATTTGAC[A/T]TTGAAAGTTTTTAAA | 115426 |
rs12346381 | snp | A/C | 0.109814 | 0.206997 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448171 | aatgtttcaaagttg[A/C]aaaaagacagagtac | 115426 |
rs12346455 | snp | A/G | 0.447809 | 0.152878 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469651 | GACACATAGGACTTG[A/G]TGAAAGgtgtgtgtg | 115426 |
rs12347573 | snp | A/G | 0.440195 | 0.162252 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472503 | ACTTCCAAAACTGGG[A/G]GAATATTGTTCTCAT | 115426 |
rs12347795 | snp | C/G | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419495 | TTAAAAAATAAAAAC[C/G]TACTGATAATGCTTT | 115426 |
rs12349901 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456188 | GGCTACATGTAAAAA[C/G]Tagaatctgtttttt | 115426 |
rs12351293 | snp | A/G | 0.366679 | 0.221102 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448615 | TGTGTGTTAGTAATT[A/G]TAAGAGGAGGATGGA | 115426 |
rs12351492 | snp | A/G | 0.287606 | 0.247155 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415338 | ACTTGGGTTTCTTCA[A/G]CCCAGTGATAAACCA | 115426 |
rs12352226 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463439 | TTAGGAACACAATAG[C/T]TAAAAAGGAACCAGT | 115426 |
rs12352596 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428476 | CTTATTTATGCAACC[C/T]TAATCCCTAATTTTC | 115426 |
rs12375531 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6429543 | gccatgttggccaga[C/T]tggtctcgaactcct | 115426 |
rs12376117 | snp | C/G | 0.495252 | 0.0484902 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411838 | GGCAAATGTGAAGTC[C/G]AAGTTGTCTTGTTTT | 115426 |
rs12378272 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467620 | tttttttttttttGG[G/T]ATTTTAACATCTCTG | 115426 |
rs12551361 | snp | G/T | 0.272511 | 0.248984 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448621 | TTAGTAATTATAAGA[G/T]GAGGATGGAGGCAAG | 115426 |
rs12553726 | snp | A/T | 0.00475057 | 0.0485048 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473312 | tagtaacacagtcag[A/T]atggaagttgttaga | 115426 |
rs12554047 | snp | A/G | 0.286042 | 0.247388 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450183 | TCAAATAACCAATCA[A/G]TGTTCATAGTTCCTT | 115426 |
rs12555191 | snp | A/G | 0.0147412 | 0.0845772 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450123 | acactgacataCAAA[A/G]TGTAACAACAAATGT | 115426 |
rs12555617 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419406 | CAGATCGATAGAATT[A/G]GAGAACTTCAGGCAA | 115426 |
rs12686562 | snp | A/G | 0.332568 | 0.235971 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451751 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 115426 |
rs13283381 | snp | C/G | 0.4444 | 0.15719 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503517 | ACTTTTTATAATTTC[C/G]TCCTACTGTAAATAA | 115426 |
rs13283464 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473103 | ctcctggctgggggc[A/C]gaaaatgggcaagat | 115426 |
rs13283631 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491191 | CTTGAGAAGTAGTTT[C/G]CTCagtgttcaggag | 115426 |
rs13283662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428530 | GGAACCATATTGCTT[C/T]TGCTTTTTTTTtttt | 115426 |
rs13283663 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428531 | GAACCATATTGCTTT[C/T]GCTTTTTTTTttttt | 115426 |
rs13283687 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473296 | taaatccatgagtcc[A/G]tagtaacacagtcag | 115426 |
rs13283688 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6428571 | ttttttttttttttt[G/T]gaacgatctcattct | 115426 |
rs13284032 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498676 | TGCCCATGCTCAGCT[G/T]TTAACCCATAAAGAC | 115426 |
rs13284392 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452034 | TATATGTGTATTTAT[A/G]CATATATACACtaga | 115426 |
rs13284998 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461911 | TGTATATGCATTTTT[A/G]TGCATTTCTTTTCTT | 115426 |
rs13285035 | snp | C/T | 0.093417 | 0.194889 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491371 | AATGAATTAATTATA[C/T]GTAAAATGCTTCTCC | 115426 |
rs13285071 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422720 | ggtcaagtgatcttc[C/G/T]tgctcggcctcccaa | 115426 |
rs13285125 | snp | G/T | 0.0988009 | 0.199095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490861 | TGTTTATATATTTTA[G/T]AAGCATTTTCAACTT | 115426 |
rs13285152 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456081 | TATTAGGAAATATAC[A/G]TACAGCCAAGTTACT | 115426 |
rs13285185 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461347 | tccctccctccctct[C/T]tctctcccccccctc | 115426 |
rs13285458 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456258 | tggtatctcagtgtg[A/G]ttttgatgtgcgttt | 115426 |
rs13285609 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416536 | GTGGATCTCTAAATC[C/T]ttttttttttttttt | 115426 |
rs13285688 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461678 | cgcccagctTTCTAT[C/T]ATTAATTTTTTAAGA | 115426 |
rs13285733 | snp | C/T | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507475 | ttgatctcctgacct[C/T]gtgatacgcctgcct | 115426 |
rs13285870 | snp | C/T | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507529 | ataggcatgagccac[C/T]gcactcggccCTCAG | 115426 |
rs13285949 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491535 | ATTAAAGGAGTTTGG[A/G]GAATGTTTGTCTTCA | 115426 |
rs13286720 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494216 | GTAATTTAAGTGAAA[C/T]TGAGAATAAGGTGGC | 115426 |
rs13288601 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426949 | agacaagatttcacc[A/G]tgttggctaggctgg | 115426 |
rs13288875 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489597 | gttgctgttttttgt[C/T]ttagccattctgata | 115426 |
rs13289916 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6422721 | gtcaagtgatcttcc[G/T]gctcggcctcccaaa | 115426 |
rs13289925 | snp | A/G | 0.429238 | 0.174281 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483120 | cgcttgaggccagga[A/G]ttcaaaaccagcctc | 115426 |
rs13290027 | snp | A/C | 0.14665 | 0.227637 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504855 | GTAAATGCATGTTTT[A/C]ATTAGATAGTGATAA | 115426 |
rs13290037 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461346 | ctccctccctccctc[C/T]ctctctcccccccct | 115426 |
rs13290126 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492715 | TGCTAGTGTTAGTAG[A/G]ATTAATTGTGCACTG | 115426 |
rs13290488 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483440 | ctataatacctaata[A/G]agtgtaaatgctatg | 115426 |
rs13290790 | snp | G/T | | | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507504 | ctcggcctcccaagg[G/T]gctgggattataggc | 115426 |
rs13291472 | snp | A/G | 0.4444 | 0.15719 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478065 | AATGCAAATCTGATC[A/G]TGTTGCTTTGTTGCT | 115426 |
rs13291494 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453939 | GGATTGAAATGGAGA[A/G]GAGTAGAACTATAGA | 115426 |
rs13291887 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486539 | ATGATTATTTACTAG[C/T]TATTGTGCAACTCAG | 115426 |
rs13292030 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501212 | AAAGGAATCACAGTT[A/G]ATTAATGTGTGGGCT | 115426 |
rs13292799 | snp | A/G | 0.396727 | 0.202413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448764 | GAGTAACAGGAGTTA[A/G]GAATGTGGTAGGTTG | 115426 |
rs13293015 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445171 | TTGGTTTGAATTCCA[C/G]GTCTTTAGTTTATTA | 115426 |
rs13294924 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484019 | GTTTCTCAGAGGCAG[C/G]CACTTTAAAATTTTA | 115426 |
rs13296481 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469937 | AAATTCTAAGCAGGA[C/T]AAATATAAAGAAAAT | 115426 |
rs13296692 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484689 | actgggattacaggt[A/G]tgagccactgtgcct | 115426 |
rs13296970 | snp | A/C | 0.399432 | 0.200425 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493297 | AGCAAGACTCTGTTT[A/C]AAAAAAAAAAGTTAA | 115426 |
rs13297077 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6487183 | TTTATTTttttttcc[C/T]ttttttttttttttt | 115426 |
rs13298500 | snp | A/T | 0.423413 | 0.180077 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502612 | ATTACTATCTGAAAC[A/T]GTTTTTGTTTGTTTA | 115426 |
rs13299896 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475633 | TTTCAAGACAACAGT[G/T]TTGATCTAAGATTCA | 115426 |
rs13299998 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454031 | aattgacatttactt[A/T]acccccattatgtac | 115426 |
rs13300059 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490342 | GTAGCAGAATATTAA[A/G]TAAggccagtcacag | 115426 |
rs13300829 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416535 | GGTGGATCTCTAAAt[A/C]ttttttttttttttt | 115426 |
rs13301146 | snp | C/T | 0.399611 | 0.200291 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493295 | AGAGCAAGACTCTGT[C/T]TAAAAAAAAAAAGTT | 115426 |
rs13301891 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416847 | CTTTTGAGAATCCAG[A/C]GCTTTTCCTATTTTA | 115426 |
rs13302032 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455809 | ggcaacatggtgaga[C/G]cctgtctccacaaaa | 115426 |
rs13440427 | snp | C/G | 0.355096 | 0.226837 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451847 | ggagtgcagtggcac[C/G]atctgggctcactgc | 115426 |
rs16924562 | snp | G/T | 0.316 | 0.241131 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450551 | TAATACTTTTCTGTG[G/T]TAAGATTCAGGTGTT | 115426 |
rs16924591 | snp | C/T | 0.228253 | 0.249052 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462585 | TACACAGTAGGATAA[C/T]AGCACACATAGCATT | 115426 |
rs16924624 | snp | A/C | 0.424968 | 0.178567 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480538 | CTTTCGCTTCACCTG[A/C]AACTCCTTAACCTTA | 115426 |
rs16924626 | snp | C/G | 0.422 | 0.181428 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480726 | AGTTTATTTTTGGAA[C/G]CCTTCCTGATTTCCC | 115426 |
rs16924628 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480751 | TTTCCCAACTAGAAA[A/G]GACTTTACTTCATAG | 115426 |
rs16924631 | snp | C/G | 0.308661 | 0.24302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486308 | CAAGAAGATGGATTT[C/G]AGAAATTTAGGAGGT | 115426 |
rs16924634 | snp | A/C | 0.286042 | 0.247388 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495789 | GTGAGTTGACAGTGC[A/C]AGTTAGTGGTGGCAG | 115426 |
rs17852551 | snp | A/C | | | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481729 | AGAAAGCAAAGATGC[A/C]GTCAGCTAGTACTGA | 115426 |
rs17852552 | snp | A/C | | | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460787 | CGTGTGAAAATTTTC[A/C]TGGGGTAAGATTGTC | 115426 |
rs17856811 | snp | A/C/T | 1.6659e-05 | 0.00288604 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477633 | ATAGGGCGAAATGAC[A/C/T]CTGAATGTGACCTGT | 115426 |
rs28501137 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489641 | ATCTTATTGTTGGAC[C/G]TGATTCGTTTGCTTA | 115426 |
rs28529307 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462299 | TCTGGCTCTTCGTGG[A/G]AAAAGTTTGCTGACT | 115426 |
rs28599170 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455836 | AAAAAGTTTTAAAAC[C/T]AGCCAGGCATAGTGG | 115426 |
rs28600190 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462209 | GTATTATCTGTGGCT[A/G]TTTTTGTGCTCCACA | 115426 |
rs28609598 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466550 | ATCTCAAAAAAAAAA[A/G]GAAAAAAAAAAAAAA | 115426 |
rs28615746 | snp | C/T | 0.15698 | 0.23205 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411160 | TTGTGGTTTTTGCCA[C/T]CGAAAGAAATGGCAA | 115426 |
rs28624357 | snp | C/T | 0.0126979 | 0.078662 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411499 | TCTCCTGCCTCAGCC[C/T]CCCGAGTAGCTGGGA | 115426 |
rs33962342 | snp | C/T | 0.232985 | 0.24942 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506038 | TTTACCATAGGATTG[C/T]CTACAGCGCTCCTTT | 115426 |
rs34041516 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498817 | CTCCCATCATTCCCC[-/C]ATTGTTGTGCTTCCC | 115426 |
rs34069701 | in-del | -/T | 0.499853 | 0.008585 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489729 | CTAATTGGGTTTTTG[-/T]TTTTTTTTTTTTTTT | 115426 |
rs34094286 | in-del | -/A | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413190 | CTCCATGTGGGAGCT[-/A]CCAGCTCTATAAGTA | 115426 |
rs34102086 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463789 | AAAAATTTTTTTTTT[-/T]AATGATTAGAAATCT | 115426 |
rs34137836 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6421458 | TGCTCTGTCACCCAG[-/G]CTGGAGTGCAGTGGC | 115426 |
rs34219128 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6425075 | TACTCCCACACCTCC[-/C]TTCCTGTCTTTCCAT | 115426 |
rs34219217 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445125 | GCAAAACCCTATCTC[-/T]TTATTTAAAAAAAAA | 115426 |
rs34229458 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6460236 | TTTATTCTAGAAAAA[-/A]TTGTATATAGCTCCC | 115426 |
rs34294660 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445151 | AAAAAAAAAAAAAAA[-/A]GATTTTGGTTTGAAT | 115426 |
rs34331170 | in-del | -/ATAC | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412157 | AGATTCCGTCTCTAA[-/ATAC]ATACATACATACATA | 115426 |
rs34366483 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467617 | TTTTTTTTTTTTTTT[-/T]GGTATTTTAACATCT | 115426 |
rs34371545 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492854 | TTTTTTTTTTTTTTT[-/T]ACATTTAGTAGATAC | 115426 |
rs34386249 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449243 | GTTTGAAGCAAAGCT[A/G]TGCTCTTTCTTGGCC | 115426 |
rs34467386 | in-del | -/A | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6413107 | GGTCTGTAACCCTCT[-/A]CCCGGGCCGCTTCCT | 115426 |
rs34487810 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469098 | ATCAGAGAAACTTTC[-/C]AAGTAACTGTGATTA | 115426 |
rs34497002 | in-del | -/A | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483325 | AAAAAAAAAAAAAAA[-/A]TCCTTTATACAATGG | 115426 |
rs34529113 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487462 | ATCTCCTCCTCCCAG[A/G]TTCAAGCGATTCTCC | 115426 |
rs34530211 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452525 | AGAAATATGATATGG[A/G]TTGAAAGGTGTGATC | 115426 |
rs34552859 | in-del | -/AA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6466571 | AAAAAAAAAAAAAAA[-/AA]GCTACAGATGCATTT | 115426 |
rs34581400 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472112 | CATCACTCCCAAAAG[G/T]TCCCTTGGGTCCCAT | 115426 |
rs34648994 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6505247 | AGTTAACTGTATGTT[-/A]TAATGTATTTAGTGC | 115426 |
rs34660246 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6432305 | CCTCTTCTGGTAGTG[-/C]ACAGTTGATAGTTTT | 115426 |
rs34667931 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498534 | AGGGGAAGGGTGGGG[-/G]AGGTGGCTTTATAAG | 115426 |
rs34676165 | in-del | -/T/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423650 | TTTTTTTTTTTTTTT[-/T/TT]AAAGAAAAGTCTCGG | 115426 |
rs34708091 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6454131 | GGTACGTTTTACGGG[-/G]TTAGGAATATAGTCC | 115426 |
rs34723879 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463882 | ATAGGCATTTTGGGG[-/G]CTGTTAGAAACAGTG | 115426 |
rs34757017 | in-del | -/T | 0.0667028 | 0.170006 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451467 | CCTAGTTTTTTTTTG[-/T]TTTTTTTTTTTGTTT | 115426 |
rs34815980 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6484810 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTTTTGC | 115426 |
rs34882868 | in-del | -/CAAAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424127 | AATTAGGCAGGAGAA[-/CAAAA]TAAAGTGTAAATATT | 115426 |
rs34892051 | in-del | -/C | 0.224709 | 0.248717 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450315 | CCCTTCCCCCCCCCC[-/C]ATTTATTTAAATAAA | 115426 |
rs34905133 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487393 | TTTTTTGAGGCGGAG[G/T]TTTACTCTTGTCACC | 115426 |
rs34918540 | in-del | -/GT/GTGT/GTGTGT | 0.468031 | 0.217569 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469657 | TGTGTGTGTGTGTGT[-/GT/GTGT/GTGTGT]ATGTATATATATACA | 115426 |
rs35026085 | snp | A/C | 0.444444 | 0.157135 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492483 | TTAAAAAATATGTAG[A/C]CCTTAATATTGGATT | 115426 |
rs35039815 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6423365 | TAAAACATGACAAAA[-/C]AGCACATCAGCTTCA | 115426 |
rs35091432 | in-del | -/A | 0.410399 | 0.191761 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425774 | CAAAGTAAATAAATT[-/A]AAAAAAAAAAAATCA | 115426 |
rs35114319 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430031 | TGGCTTTTCTTTTTT[-/T]GAAATGGAGTTTTAC | 115426 |
rs35199631 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461667 | TGAGCCACTGCGCCC[-/C]AGCTTTCTATTATTA | 115426 |
rs35206063 | in-del | -/T | 0.43598 | 0.167067 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434449 | CTCTATTAGGTGGGC[-/T]TTTTTTTGAGATGGT | 115426 |
rs35236011 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6486743 | TCTTTAGGTACCAAG[-/C]AATATATATGAAAGC | 115426 |
rs35301257 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442076 | GTTCAACAATTCTCA[A/T]GCCTTAGCCTGTCGA | 115426 |
rs35314530 | in-del | -/T | 0.476634 | 0.105533 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446160 | ACCTCACCTGGATAA[-/T]TTTTTTTTTTTTATA | 115426 |
rs35317708 | in-del | -/TA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469737 | ATACGTGTATATATA[-/TA]CACGTATATATACAC | 115426 |
rs35325264 | in-del | -/TTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504016 | TTTTTTTTTTTTTTT[-/TTTT]AAGACCGAGTCTCGC | 115426 |
rs35344155 | in-del | -/C | 0.0547245 | 0.156101 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424014 | GGTTAATATTTTAAA[-/C]CACATTCTATACCGG | 115426 |
rs35372848 | in-del | -/AA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6464662 | ACTGTTTATTGAAAA[-/AA]GCCCATTTCCCTCCC | 115426 |
rs35379052 | in-del | -/A | 0.158302 | 0.232576 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412271 | AGGCGGGGTGGGGGG[-/A]TGGGGGAAGCCCTGT | 115426 |
rs35408061 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469738 | TGCATATATACGTGT[A/G]TATATATACACGTAT | 115426 |
rs35519486 | in-del | -/TC | 0.0437281 | 0.141251 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443574 | AAAAATTTCTGTTTA[-/TC]TCTCTAGTCAGAATG | 115426 |
rs35614468 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504860 | GCATGTTTTCATTAG[-/C]ATAGTGATAATAATT | 115426 |
rs35656211 | in-del | -/C | 0.359364 | 0.22481 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455790 | GGAGTCTGAGACCAG[-/C]CTGGGCAACATGGTG | 115426 |
rs35677276 | in-del | -/T | | | frameshift-variant, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460785 | TCGTGTGAAAATTTT[-/T]CCTGGGGTAAGATTG | 115426 |
rs35690339 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417312 | GCTTCTTAAGTATTG[G/T]AAATACTGCATCTCC | 115426 |
rs35764668 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442666 | GATTTTTTTTTTTTT[-/T]GGGGGGGTAGAGATG | 115426 |
rs35853520 | in-del | -/T | 0.380919 | 0.21298 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442653 | CCAGTTAATTTTTGA[-/T]TTTTTTTTTTTTTGG | 115426 |
rs35859975 | in-del | -/A | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470375 | AAAAAAAAAAAAAAA[-/A]TTTCCCAACTTAAAA | 115426 |
rs35934099 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6436775 | TTTGGCAACTTTTTT[-/T]GTCAGTTAGAATGAA | 115426 |
rs35959685 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6474026 | CTTTTCAAACACAGG[-/G]CAAAACTGTTTTAGG | 115426 |
rs35964399 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424793 | TTTTTTTTTTTTTTT[-/T]CAATTACCGTGACCA | 115426 |
rs35999789 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6430053 | GAGTTTTACTCTTTT[-/T]GCCCTGAAGTGCAAT | 115426 |
rs35999933 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504393 | TGGATATATTTTGGG[-/G]ATACATGTGAAATTT | 115426 |
rs36004565 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6451973 | AATAAAAGTGTATTG[G/T]GTATATATGCATTTG | 115426 |
rs36009417 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6417006 | ATAAAAGTACTTGCC[-/C]TATTTAAAGGAATAT | 115426 |
rs36040837 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442326 | TGTCAGATTCTTCCC[-/C]TGATTGTAAAATGCT | 115426 |
rs36089474 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452673 | AAAGGCAACATAAGA[C/T]AAATTGGAGATAACT | 115426 |
rs36091755 | in-del | -/AG | 0.454664 | 0.143571 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424381 | TAGTGGTCACAATTA[-/AG]AGAGAATTTTTAGCA | 115426 |
rs36108024 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507024 | ATATTCCCTAAAGTA[C/T]ACCTTAATAAATATT | 115426 |
rs41281761 | snp | A/C | 0.00926743 | 0.0674376 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6475424 | AAATGACTGCAAGAT[A/C]ATATCTGTAGATGAA | 115426 |
rs41281763 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486678 | TTTAGGTACCAGGAG[A/G]TTTAAAATGAGAGAG | 115426 |
rs41281765 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498287 | GGTGAGGAATAAGAT[C/T]ATGCAAATAGACAGA | 115426 |
rs41281767 | snp | G/T | 0.00345114 | 0.0413964 | intron-variant | UHRF2 | GRCh38.p7 | 9:6506001 | CATGCTTTATGCTCA[G/T]ATTAAATTGGATGTT | 115426 |
rs41306063 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415643 | AGTGAAAAATGTCAT[A/G]AATTGTAGACAATAC | 115426 |
rs41313446 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414479 | GCTGTCTGTGGGCAT[A/C]TCTGGTATTTTTATG | 115426 |
rs55765959 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430769 | TGGAAAACACAATAA[A/T]GGCTCTGGGCCCTAA | 115426 |
rs55832887 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459365 | GAGGCCATCATCTAG[C/T]CCTGTTAAAACTTAA | 115426 |
rs55849474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470070 | TGGCATGTGAAAATA[C/G]TAATTTAAAAACATT | 115426 |
rs55960819 | snp | A/T | 0.225597 | 0.248806 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459121 | TACCTAATGTAGATG[A/T]CAGGTTGATGGGTGC | 115426 |
rs55988623 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496064 | AAGTTATTTTTTAAA[A/G]CAAAATACTTTCAAG | 115426 |
rs56029722 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6496325 | TCCTAGAGGAAAATG[C/T]TAATTTTAAACTGAT | 115426 |
rs56218473 | snp | A/G | 0.406641 | 0.194842 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432790 | TTAAGGGCTTAAAAA[A/G]AAAGTTGAAGGAATT | 115426 |
rs56268419 | in-del | -/TATA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6469710 | ATATACATACATATA[-/TATA]CACACATATATGTGC | 115426 |
rs56270454 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431478 | GTGTGGTGGCATATA[C/T]CTGTAGTCCTAGCTG | 115426 |
rs56396114 | snp | C/G | 0.309648 | 0.24278 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448582 | GTTATAAGTATATGT[C/G]AACGCTTAATGCAGT | 115426 |
rs56411118 | snp | C/T | 0.23846 | 0.249734 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421475 | TGGAGTGCAGTGGCG[C/T]ACGCAATCTTGGCTC | 115426 |
rs56685965 | in-del | -/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416560 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGT | 115426 |
rs56803438 | in-del | -/C/CC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445974 | TACTCTTCCCCCCCC[-/C/CC]GCCACCCTTTTTTTT | 115426 |
rs56939673 | snp | A/G | 0.309894 | 0.242719 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423672 | AAGTCTCGGCCGGGC[A/G]TGGTGGCTCACACCT | 115426 |
rs57099869 | in-del | -/C | 8.41007e-05 | 0.00648408 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499822 | TGTACTCTCCCTCCT[-/C]CCCCCCCATCAGTAT | 115426 |
rs57147850 | in-del | -/T/TTTTTT | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446000 | TTTTTTTTTTTTTTT[-/T/TTTTTT]CCTGTTTTTGAGATA | 115426 |
rs57198563 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446691 | ACCCCGTCTCTATAG[A/G]AAAATTTGCTTGGTG | 115426 |
rs57868028 | in-del | -/AAAAAAAAAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6485819 | AAAAAAAAAAAAAAA[-/AAAAAAAAAA]CAAAACCCAAAACCA | 115426 |
rs57935657 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494991 | AGGAGCTTAGCTATT[A/C]TTTTCTAGCAAGAAA | 115426 |
rs58171060 | in-del | -/T | 0.0991586 | 0.199366 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435000 | ACCATGTTTGGCTAG[-/T]TTTTTTTTTTTTTAA | 115426 |
rs58190928 | in-del | -/T | 0.372995 | 0.217652 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454029 | CTAATTGACATTTAC[-/T]TTACCCCCATTATGT | 115426 |
rs58280407 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488564 | TTTTTTTTTTTTTTT[-/T]GAGATGGAATCTTGC | 115426 |
rs58560960 | in-del | -/C | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412184 | ATACATACATACATA[-/C]ATAATAAATAAAATA | 115426 |
rs58561913 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431538 | CTGCGGAGAGCTGTG[A/G]TCACACCACTGCATC | 115426 |
rs58586889 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486027 | CAGGCATATATGTTC[A/C]TTGAAGGAGAAGCTG | 115426 |
rs58682419 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6456503 | TTCACTCTGATGATA[A/G]TTTCTTTTGCTGTGC | 115426 |
rs58693786 | in-del | -/G/GTTTTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445984 | CCCCCGCCACCCTTT[-/G/GTTTTTT]TTTTTTTTTTTTTTT | 115426 |
rs58718382 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457468 | CAGGGACAATTTGAC[C/T]TCCTCTTTTCCTAAT | 115426 |
rs58756210 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483411 | CTTTATATGTTAAAT[C/T]ACCTCTAGATTACCT | 115426 |
rs59140789 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416811 | GGATTACAGGCGTGA[C/G]CCACCGCGCCCGGCC | 115426 |
rs59181243 | in-del | -/CT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443579 | TTTCTGTTTATCTCT[-/CT]AGTCAGAATGCTTTC | 115426 |
rs59303772 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469862 | CAGTATTTGAAAATA[C/T]AGTAGCCCAAAATTT | 115426 |
rs59497678 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6444477 | CCCTTTACATTTATG[C/T]TTCTCAAAGATGGTC | 115426 |
rs60428309 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483073 | GCTCACACCTGTAAT[C/T]TCAGCACTTTGGAAG | 115426 |
rs60458534 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6450309 | TCTTCCCCTTCCCCC[-/C]CCCCCCATTTATTTA | 115426 |
rs60522189 | in-del | -/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416560 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGT | 115426 |
rs60664493 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457957 | TCATAGGGATATTGG[C/T]CTGAAATTTTCTTTT | 115426 |
rs60812725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443558 | TTTGTTTAAATAACT[C/T]AAAAATTTCTGTTTA | 115426 |
rs60874824 | in-del | -/A | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462010 | TTAAAAAAAAAAAAA[-/A]TAAGAGAAACAGCTA | 115426 |
rs61061078 | snp | C/T | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419332 | CAAAATATGGGTGGG[C/T]TGCAAATAATTTATT | 115426 |
rs61211445 | in-del | -/TTC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6446001 | TTTTTTTTTTTTTTC[-/TTC]CTGTTTTTGAGATAG | 115426 |
rs61336186 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6504046 | TTTTTTTTTTTTTAA[A/G]ACCGAGTCTCGCTCT | 115426 |
rs61371978 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6461360 | CTCTCTCTCCCCCCC[-/C]TCCTCCTCTCCCCCT | 115426 |
rs61454062 | in-del | -/A | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503415 | GCTTAAAAAAAAAAA[-/A]CCAGCCAAGATGAAA | 115426 |
rs61760197 | snp | A/G | | | splice-donor-variant | UHRF2 | GRCh38.p7 | 9:6482100 | AGATTTAGAGTTCAG[A/G]TATGTTTTAACTTGG | 115426 |
rs61998182 | snp | C/T | 0.0266618 | 0.112339 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420986 | GCTAGTTCGCCCAGA[C/T]CCTGATCATCTTCCT | 115426 |
rs62566133 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445126 | CAAAACCCTATCTCT[A/T]ATTTAAAAAAAAAAA | 115426 |
rs62566134 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452276 | GTATCTTTTCATCAG[G/T]ATTTTATTTATGTCC | 115426 |
rs62566150 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463489 | TTTTTTTTTTTTTGG[G/T]AGATGGGGTCTCGCT | 115426 |
rs62566151 | snp | C/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465296 | TACATGTTAATTTTC[C/T]TATCTCAGTGTCCTT | 115426 |
rs62566152 | snp | A/G | 0.106278 | 0.204558 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479068 | TACTAGATCATTCTC[A/G]TTAGCATTCTAGAAT | 115426 |
rs62566154 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504844 | ACGTCTTGGTGGTAA[A/G]TGCATGTTTTAATTA | 115426 |
rs63177262 | snp | A/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489746 | TTTTTTTTTTTTTTT[A/T]ACCATTCATCAGATA | 115426 |
rs66509816 | snp | A/G | 0.321053 | 0.23969 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486591 | GAATTCTCAGAACCT[A/G]AAGGATATGTTTGAG | 115426 |
rs67797327 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480658 | ACAGAATCTTTAATA[A/C]AGTTAGTTATAAAGA | 115426 |
rs71328187 | in-del | -/AACAAC/AACAACAAC/ACAACAACAAC | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451799 | AGACTCTGTCTCAAA[-/AACAAC/AACAACAAC/ACAACAACAAC]AACAACAACAACAAC | 115426 |
rs71328188 | in-del | -/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462010 | TAGCTGTTTCTCTTA[-/T]TTTTTTTTTTTTAAA | 115426 |
rs71328189 | in-del | -/G | 0.0441095 | 0.141807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477525 | ACAGCATTTTTTTTG[-/G]AAATGGAGTTTTGCT | 115426 |
rs71328190 | in-del | -/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485828 | TGGTTTTGGGTTTTG[-/T]TTTTTTTTTTTTTTT | 115426 |
rs71328191 | in-del | -/A | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488830 | GTGAGACTCTATCTC[-/A]AAAAAAAACAAAACA | 115426 |
rs71328192 | in-del | -/TC | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490016 | AACATCTTTTGTATT[-/TC]TGACAAATATACAAA | 115426 |
rs71487848 | in-del | -/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418278 | TTTTTTTTTTTTTTT[-/T]AAATCAAGGAAGCAA | 115426 |
rs71490273 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488546 | TTTTTCTTTTCTTTT[C/T]TTTTCTTTTTTTTTT | 115426 |
rs71490274 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488551 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTGA | 115426 |
rs71505810 | snp | C/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414213 | GGGTTTCCAGAACTT[C/T]TGGTCCCTCTCCCTC | 115426 |
rs71505811 | snp | C/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414239 | CCCTCGCCGCCTTTC[C/T]TAGGTTTGGAATGTC | 115426 |
rs71505812 | snp | G/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423505 | TTTAAGCAAATATGG[G/T]TTGTCAGGATGTGGG | 115426 |
rs71505814 | snp | C/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484517 | AAGCTGTCCTTTACT[C/T]TGAGCCACCAGAGTA | 115426 |
rs71505815 | snp | C/G | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499242 | ACAAAGCATGCTTCT[C/G]CCACCCCACCCACCC | 115426 |
rs71505816 | snp | C/G | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499249 | ATGCTTCTCCCACCC[C/G]ACCCACCCCCTCAAA | 115426 |
rs72499188 | snp | C/G | 0.00128092 | 0.0252748 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486770 | AAGCATTTTGTAAAT[C/G]TATCTTAACTGTTCA | 115426 |
rs72693585 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6449334 | TAATTTCACACCTGA[A/G]CTTACCATTAGACTG | 115426 |
rs72693587 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469163 | TTGGAATTCACAAAA[G/T]AATTATATGGAGATT | 115426 |
rs73394299 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502429 | CTTCCCAAACTACCC[A/T]TTCTAAAATGGCAAC | 115426 |
rs73399080 | snp | A/G | 0.309648 | 0.24278 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475805 | TATTTTGATACAGGC[A/G]TACAGTGTGTAAATG | 115426 |
rs73399085 | snp | C/T | 0.0600885 | 0.162584 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477791 | ACCTTTGGATAAAGT[C/T]CCAGAAGAGGAATAC | 115426 |
rs73399089 | snp | G/T | 0.0633504 | 0.166319 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478881 | TGATCACACTCTGAA[G/T]TTTACCATCGCTAAT | 115426 |
rs73399099 | snp | C/G | 0.0622301 | 0.165053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480564 | CCTTAAATCTTTTCT[C/G]CTTCTCCAAATCATG | 115426 |
rs73399664 | snp | A/G | 0.0414363 | 0.137845 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419554 | TTTTTTAAAAAAGTG[A/G]AACACTGAGCTGATG | 115426 |
rs73399669 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422228 | GTGGGATTACAGGCG[C/T]GTACCACCATGCCTG | 115426 |
rs73399673 | snp | A/T | 0.0501905 | 0.150254 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423987 | ACTCTTGATAAGAGG[A/T]ATAGACAGAATAGGT | 115426 |
rs73399684 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428091 | TTACAGTTTAGCTGA[A/G]CATGTGGCACTGTTA | 115426 |
rs73399687 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428645 | GCCCCAACCTTCTGG[C/G]CTTAAGCGATCCTGC | 115426 |
rs73399691 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429216 | AACAATTTTCAGAGT[C/T]GGAGAACCTGTATTC | 115426 |
rs73399700 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429936 | GGTATTTTCTTTTTT[A/T]AATGATTGCCCCTTG | 115426 |
rs73399702 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429983 | TTTTAAAAATATTAG[A/G]TATTTGGACAGGGGA | 115426 |
rs73401017 | snp | C/G | 0.0839998 | 0.186933 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490301 | CTTTGCACATAGCAC[C/G]GACTCAAATGTTAGT | 115426 |
rs73401025 | snp | C/T | 0.347694 | 0.230122 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492741 | CACTGATAGTTACTT[C/T]TCTTAATTTGTTTCA | 115426 |
rs73401678 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436621 | GAATAAGGAACTTTA[A/C]ATAGTGAACTAAGGC | 115426 |
rs73401679 | snp | C/T | 0.372391 | 0.217992 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436677 | CTCTTAAAGTTGCTT[C/T]TGAAGTAAGACTATC | 115426 |
rs73403410 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460877 | ACGTGTACCTTAGTA[A/C]AAAAAGATGGAGTCT | 115426 |
rs73403414 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468158 | AGATTCAGTGAAATA[A/G]GATATTTCTTGGGGA | 115426 |
rs73639303 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451079 | TTAACCTGAAAATCA[C/T]AGTTCCTAGTGATAT | 115426 |
rs73639304 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467854 | GAGGATGCTTTTTTT[C/T]CCTTATACCCAGTGG | 115426 |
rs73639305 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473761 | GCATGAAACCAGCCA[C/T]AGATAATACAAAAAT | 115426 |
rs73639306 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486061 | ATAAGGCTAGGAAAA[A/G]TAGATAGGAGCCATA | 115426 |
rs73639308 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505693 | CAGATTTTTTTTCCC[C/T]CTCTAGGGCTCTGTT | 115426 |
rs73642515 | snp | A/G | 0.00890296 | 0.0661227 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422679 | CAGTGACGTGAACAC[A/G]GCTCGCTGTAGCCTT | 115426 |
rs73642516 | snp | A/T | 0.0551013 | 0.156571 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424798 | TTTTTTTTTTTCAAT[A/T]ACCGTGACCATTTTG | 115426 |
rs73642517 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426083 | AAAGTTCAGCAGTTT[C/G]GGTCAACTTAAATTT | 115426 |
rs73642519 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437115 | AGAAAAATGAATTAT[A/G]AAATATAATGAAGTA | 115426 |
rs73642520 | snp | C/G/T | 0.0154538 | 0.0865337 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443591 | TCTCTAGTCAGAATG[C/G/T]TTTCACAGAACAGAT | 115426 |
rs73642521 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444328 | CCTGAGTGGATGGTA[A/G]TCAAAAGGAGGAAGG | 115426 |
rs74401453 | snp | A/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484430 | CTCCCTCCTCCCTCC[A/T]GTCTCTTCCCTCCTC | 115426 |
rs74573824 | in-del | -/G | 0 | 0 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420435 | ATGGCCGGGTGCGGT[-/G]GCTCACGCTGTAATC | 115426 |
rs74692754 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415441 | CTGTGTGTTCACTTT[C/T]TTATGCGCTGACAAG | 115426 |
rs74729885 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471869 | GGTTCCAAACTAAGT[A/G]GGACCAGGAGAATAG | 115426 |
rs74736829 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501977 | TCCCACTGGGACAGA[A/T]TCTGACCTTCCTAGG | 115426 |
rs74754610 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448401 | CTACATAGTTTCTAT[A/G]ATATGTTCAAGAAGA | 115426 |
rs74781935 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469119 | ACTGTGATTAATATG[A/C]TGAAAACATGGTGAA | 115426 |
rs74898627 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471797 | CTCTTTAAATTGGTC[A/G]GTTAAAGCTCCATTC | 115426 |
rs74964525 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6499422 | ACCCTTAATGTTCTT[A/G]ATATTTTTTTAGATC | 115426 |
rs75154171 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6463442 | GGAACACARTAGCTA[A/G]AAAGGAACCAGTGTG | 115426 |
rs75319247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497841 | TCATGGGAAGTACTG[C/T]AATAGGAATTAAGGT | 115426 |
rs75337563 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504365 | CTGAAACATTTTTAT[G/T]GCTAAATAATAGATG | 115426 |
rs75346289 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473990 | GAGGAAAGAGATGGC[A/G]TGTGAATTTATAGAT | 115426 |
rs75474491 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6503429 | AAAAAACCAGCCAAG[A/G]TGAAATGGAGCCAGT | 115426 |
rs75484798 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444160 | TTGAATTAAGTGTCA[C/T]GTCAGTCTTGAGTAC | 115426 |
rs75526516 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454719 | CCACTTTGGTTTTGA[A/G]CAGGCCACTCTTAGT | 115426 |
rs75589375 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467997 | ATCACAGTCTTTTTT[C/T]CTTACTTGAAATTAC | 115426 |
rs75604845 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452172 | ATATTCTATTATGTA[C/T]CTGTATTATGTTATC | 115426 |
rs75813410 | snp | A/G | 0.031825 | 0.122064 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485925 | ACTTGTTTCAGTGAG[A/G]CAGGAATGAAGATAT | 115426 |
rs76249889 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499079 | GTCAAATTCACTTTC[A/G]GAAGATTTTTCAGAT | 115426 |
rs76250339 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501086 | CACAATTTTCAAAAC[C/G]TACATGTTAAACTAA | 115426 |
rs76364033 | snp | A/C | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477233 | AGTGAGACTCCATCT[A/C]AAAAAAAAAGACTGG | 115426 |
rs76402967 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429192 | AAAAGGAAGATGGTA[A/C]AATGAGAGAACAATT | 115426 |
rs76407878 | snp | A/T | 0.040671 | 0.13668 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459214 | AAGAACTTAAATTTT[A/T]AAAAAAGAAAGAAAG | 115426 |
rs76547389 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6501833 | AGCCTAATTATTCTC[C/T]GATTGGGAAAGATAG | 115426 |
rs76552338 | snp | G/T | 0.230896 | 0.249269 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465342 | GTTTCACAAAATAAT[G/T]TGGAATCTTCTTTTT | 115426 |
rs76810931 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440293 | TGCCGGACTCTGAGC[A/G]TAACTTCTTACACAG | 115426 |
rs76841223 | snp | G/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451477 | TTTTGTTTTTTTTTT[G/T]TGTTTGTTTGTTTGT | 115426 |
rs76859182 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489264 | TCTTTTTATTGATGA[A/G]TACTAGTCCATGGTG | 115426 |
rs76867248 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419302 | TGGATTAGGATTTCA[A/G]CCCATAACCCTTACC | 115426 |
rs76872189 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441465 | ATATGATGAATCAGT[C/T]CTGGAGTTGGCTGAG | 115426 |
rs76959097 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486236 | AAACTAGAGGCAGTA[A/G]AAAAAGGATCTGTTG | 115426 |
rs76982344 | snp | A/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466630 | TTATGTATTTACTAA[A/T]TTTTTTTCATACTTA | 115426 |
rs77001149 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500276 | TCCAGCCAACATACT[C/T]TTTAATAAAGAGAAA | 115426 |
rs77045370 | snp | A/G | 0.00536843 | 0.0515305 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434112 | GACAGTGTACCCTCT[A/G]CGTCTAATTCAGACT | 115426 |
rs77116152 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498808 | TTGAGTTCATCTCCC[A/G]TCATTCCCCATTGTT | 115426 |
rs77150548 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419911 | CACCCGGCTACGTTT[A/T]TTTATTTATTTATTT | 115426 |
rs77156423 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472861 | GGATTTTTCTGGTTG[A/G]GGGAAAAAGGAAAAA | 115426 |
rs77208023 | snp | A/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435013 | AGTTTTTTTTTTTTT[A/T]AATTTTAGTTTTGAG | 115426 |
rs77270598 | in-del | -/A | 0.0711525 | 0.174681 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463285 | AAACTTCGTCTCAAT[-/A]AAAAAAAAAAGACTT | 115426 |
rs77294549 | snp | A/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461378 | CTCCTCTCCCCCTCC[A/T]CCTTCTCTCCTCCCC | 115426 |
rs77422321 | snp | A/C | 0.0566069 | 0.158427 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495626 | GGGCAGCAAAGTAAC[A/C]TGGCCATCTTTTATC | 115426 |
rs77445502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465589 | ATAAATTTTTTTGGT[A/G]CCTACATCTTTTTAA | 115426 |
rs77536511 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467719 | GCTTGTTTACTAGTC[A/G]CTTGGGAGTGCCATT | 115426 |
rs77582252 | snp | G/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484577 | CCAGCTGATTTTTGT[G/T]TTTTTTTTTTTTTTT | 115426 |
rs77658815 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502349 | ACTCTGACTGGAATT[C/G]TCTTTTCATGTGTCT | 115426 |
rs77908535 | snp | C/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432853 | CATTTTTTTTTTTTT[C/T]TTTTTGAGACAGAGT | 115426 |
rs78091088 | snp | A/T | 0.030278 | 0.119257 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427973 | TCGTTTTAATTTTGG[A/T]TTTTGTGTATGGAAG | 115426 |
rs78203125 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465579 | ATCTGTTGTCATAAA[-/T]TTTTTTGGTACCTAC | 115426 |
rs78234086 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428140 | TTATGCTCATTGTAT[A/G]ATAGAAAGTACTGGA | 115426 |
rs78241981 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433359 | GGTAGATAAATGTAT[A/T]TGCCTAGTGAGTTAC | 115426 |
rs78259504 | snp | C/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492836 | AGAGCTTTTGGCTTT[C/T]TTTTTTTTTTTTTTT | 115426 |
rs78470673 | snp | A/G | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466555 | AAAAAAAAAAGGAAA[A/G]AAAAAAAAAAAAAAA | 115426 |
rs78489255 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504767 | CTGTTTTTAGCATGC[G/T]AAGAAGCATTTTCCG | 115426 |
rs78507455 | snp | C/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492856 | TTTTTTTTTTTTTTA[C/T]ATTTAGTAGATACTT | 115426 |
rs78602504 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449260 | GCTCTTTCTTGGCCT[C/T]CCTCAGCCAGTGACC | 115426 |
rs78648831 | snp | A/G | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445152 | AAAAAAAAAAAAAAA[A/G]ATTTTGGTTTGAATT | 115426 |
rs78689655 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475899 | GGAACATTCTAAATC[G/T]ATTCTTTTAGCGATT | 115426 |
rs78717340 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444450 | TTTCACCTCTTCAAA[C/T]TTATATATCGTCCCT | 115426 |
rs78737784 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491469 | TAAAGGGTGTTATGA[C/G]AGAAGTTGGTAACAT | 115426 |
rs78740892 | snp | A/C/G | 0.00835301 | 0.0641024 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449422 | CAAAATGATAGACCA[A/C/G]CATCATGGTCTAAGG | 115426 |
rs78760862 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498528 | CTCTGGTAGGGGAAG[G/T]GTGGGGAGGTGGCTT | 115426 |
rs78882563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416994 | TTTCACACAGAATAT[A/T]AAAGTACTTGCCTAT | 115426 |
rs78892976 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424655 | TATTTGTTGAAATTA[A/G]TGACCCATATTTTCT | 115426 |
rs79007768 | snp | A/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484437 | CTCCCTCCTGTCTCT[A/T]CCCTCCTCCCTCCTC | 115426 |
rs79037067 | snp | A/C | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428232 | TTAACCTTTTTGATT[A/C]TGAAATGTATTAGAC | 115426 |
rs79038012 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469965 | AATGCACAGTGGTAT[A/G]TCACAAACAAGAATG | 115426 |
rs79162222 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481305 | GTTCTAGGAAGATCT[A/G]GCTACTTTTGTTTTA | 115426 |
rs79300900 | snp | G/T | 0.010667 | 0.0722477 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6482002 | TGTAGGGAATGGCTT[G/T]TGTTGGTCGTACGAG | 115426 |
rs79301344 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480835 | AAATTTTTCTCTCCT[A/G]TAGTGCTCAACAAAG | 115426 |
rs79309408 | snp | G/T | 0.313814 | 0.241719 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463547 | ACAATCCCGGCTCAC[G/T]GCAACCTCCGCCTCC | 115426 |
rs79361723 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6480931 | AATTGTGAAATAGAA[A/C]GTATGGGCAAAGAAA | 115426 |
rs79385173 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484276 | AGACAGGGTCATGCT[A/G]TGTTACCCAGGCTAG | 115426 |
rs79434594 | in-del | -/CTA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6498607 | CTCTCTTCCCCCGCA[-/CTA]AAGCTGCTTCCCTGC | 115426 |
rs79478212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438138 | ATTATGATTGTTCCC[A/G]TATTGTAAAAGCTCT | 115426 |
rs79522542 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473149 | TGTCATGCAAATAAG[A/G]AGTCCCACAAAGTCT | 115426 |
rs79561829 | snp | G/T | 0.00438332 | 0.0466095 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507433 | TTTTAGTAAAGACGG[G/T]GTTTCACCGTGTTAG | 115426 |
rs79670759 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6478335 | TTTTCAGTTAAATGT[G/T]GCTTCCTCTGGTAAT | 115426 |
rs79685842 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482410 | AAATATTAAACTTGA[A/G]TCATGTGGCAAATTC | 115426 |
rs79718679 | in-del | -/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424386 | GTCACAATTAAGAGA[-/G]AATTTTTAGCACTGA | 115426 |
rs79762977 | snp | A/G/T | 0.0217236 | 0.101931 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450229 | AATGTACTTAGGTTG[A/G/T]TCAAATAAGGATCAA | 115426 |
rs79793188 | snp | C/T | 0.268995 | 0.249277 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449701 | AATAGTTCTCTGTGC[C/T]TAAACTGTTTTTGCA | 115426 |
rs79866523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472366 | TGAGAAAATAAGGAA[C/T]AGTATAACATGCTTA | 115426 |
rs79870962 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496865 | CTTTAGTTTTCCAAC[A/G]TTCTCCCTTCCCCCA | 115426 |
rs79975981 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473311 | ATAGTAACACAGTCA[G/T]TATGGAAGTTGTTAG | 115426 |
rs79977076 | snp | A/C | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497704 | GATTTTCAAAGCAGC[A/C]CATCATAGTAATAGA | 115426 |
rs80056198 | snp | A/C | | | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420128 | GTGGCGCAATTTCAG[A/C]TCACTGCAACCTCCA | 115426 |
rs80096444 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501225 | TTAATTAATGTGTGG[A/G]CTTTGTGTTAAGCTG | 115426 |
rs80106227 | snp | A/G | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466556 | AAAAAAAAAGGAAAA[A/G]AAAAAAAAAAAAAAA | 115426 |
rs80188408 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489500 | ACTGCCAAACTGTTT[C/T]CTCCAGTGACTACCA | 115426 |
rs80317894 | snp | A/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446173 | AATTTTTTTTTTTTT[A/T]TACAGTCTTGCTCTG | 115426 |
rs111251622 | snp | G/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421694 | AGTGCTGGAATTACC[G/T]GGGTGAGCCACCTCG | 115426 |
rs111254887 | snp | A/G | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427022 | CAAAGTGCTGGGATT[A/G]TAGGCATGAGCCACT | 115426 |
rs111255941 | snp | C/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463561 | CTGCAACCTCCGCCT[C/T]CTGGATTCAAGCAGT | 115426 |
rs111257895 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436930 | TTTCTTTGAAAAATG[A/T]AAGATAACAGAAGCT | 115426 |
rs111412415 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6452880 | AGTTGTCACTGTATA[G/T]TTTAAAATATGTGTA | 115426 |
rs111418823 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488960 | TGGGACTACAGGCAT[A/G]CATCGCCATTGACTA | 115426 |
rs111432389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479282 | ATGTCAGGTTCACAG[A/G]CACTTTTTATGTCTA | 115426 |
rs111506459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433641 | AAAGAATAATATTTT[C/G]AAAAGTCTAGTGTAT | 115426 |
rs111518641 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423668 | AGAAAAGTCTCGGCC[A/G]GGCGTGGTGGCTCAC | 115426 |
rs111520934 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446119 | TGCCTTAGCCTCCTA[A/G]GTAACTAGGACTACA | 115426 |
rs111544718 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487611 | ACCTCAGGTGATCCT[C/T]CCGCCTTGGCCTCCC | 115426 |
rs111586563 | in-del | -/A | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497592 | GTTTTTTTTTTTAAA[-/A]TGTAAGTGTATGTTC | 115426 |
rs111616743 | snp | A/G | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480037 | CTTAGAATAAAAAAA[A/G]TCTAAGCCCTTACCA | 115426 |
rs111622741 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503483 | TATCCATTTGATCAT[G/T]TTTACATTAGGTGGC | 115426 |
rs111668214 | snp | G/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445283 | TATTGATTGATTGAT[G/T]GATGGAGTCTTGCTC | 115426 |
rs111746231 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483794 | TCCCGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 115426 |
rs111760514 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6443470 | CAACTACTCTACCAT[A/G]CTACCTCTCATTTTA | 115426 |
rs111822258 | snp | A/G | 0.316243 | 0.241064 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455277 | ATATCTCCTAATGCT[A/G]TCCCTCCCCCCTCTC | 115426 |
rs111835116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437335 | CCTTGCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 115426 |
rs111875952 | snp | A/G | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466551 | TCTCAAAAAAAAAAG[A/G]AAAAAAAAAAAAAAA | 115426 |
rs111880032 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455688 | CAGGAAGTTAGGCCT[A/G]AAAGTGAAGAACCTG | 115426 |
rs112021879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489116 | CTCCCAGCCTCATTT[C/T]TTCCTGTAATTTTCT | 115426 |
rs112036350 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461306 | TTCTATCATTTCTTT[C/G]TTTTCTTTTTTTCTT | 115426 |
rs112064627 | snp | C/G | 1.65466e-05 | 0.00287628 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505999 | TACATGCTTTATGCT[C/G]AGATTAAATTGGATG | 115426 |
rs112087701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479329 | CTCATTCCTTACTCA[A/G]CTGCTTAGCTGGTTA | 115426 |
rs112089337 | snp | A/G | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496486 | TACTAAATAAGTTCC[A/G]GCTAAGTCAGGTACT | 115426 |
rs112097077 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479818 | ACATACTCTACCTCA[A/G]TAGATTTTGACAGTT | 115426 |
rs112101121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472019 | GTAATATGTACTTAC[C/T]CTTAAGTGTATCTTA | 115426 |
rs112125647 | snp | A/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499049 | AATAATTCTTTTTAA[A/T]ATAAAAATAACTTTG | 115426 |
rs112134331 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6462293 | TTACTTTCTGGCTCT[A/T]CGTGGGAAAAGTTTG | 115426 |
rs112170871 | snp | A/G | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460893 | AAAAAGATGGAGTCT[A/G]TAAAAGATGGAAATT | 115426 |
rs112214626 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496327 | CTAGAGGAAAATGCT[A/G]ATTTTAAACTGATTC | 115426 |
rs112221073 | snp | A/G | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458728 | GGTGGTGTATACCCA[A/G]AGGATTATAAATCAT | 115426 |
rs112260837 | in-del | -/ATTG | 0.0452528 | 0.143452 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445269 | CTGTGTTATTTATGT[-/ATTG]ATTGATTGATTGATG | 115426 |
rs112310586 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451475 | TTTTTTGTTTTTTTT[G/T]TTTGTTTGTTTGTTT | 115426 |
rs112348823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434329 | GGTTGTACTCTAATT[C/T]AAAGGTCCTTTTAGC | 115426 |
rs112354779 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482688 | TGCAAGCTCTGCCTC[A/G]TGGGTTCACGCCATT | 115426 |
rs112488803 | in-del | -/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484577 | CAGCTGATTTTTGTG[-/T]TTTTTTTTTTTTTTT | 115426 |
rs112523346 | snp | G/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445985 | CCCCCGCCACCCTTT[G/T]TTTTTTTTTTTTTTT | 115426 |
rs112569337 | snp | C/G | 0.0107246 | 0.0724382 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6411714 | TATACTACTGGATTT[C/G]TCTGTGCTTGTAATT | 115426 |
rs112638343 | snp | A/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450914 | TGCTGCTTACTGATA[A/T]GTGTTTGGTCATGTT | 115426 |
rs112640638 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428999 | GTGAAACCCCATCTC[C/T]GCTAAAAATATAAAA | 115426 |
rs112722427 | snp | G/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447596 | AGAAATGAAACTAAA[G/T]GTAAATAAAGATTTC | 115426 |
rs112758367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447935 | ATAGAACTAAAAACA[A/G]GAGGATTGGTTAATT | 115426 |
rs112813358 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482807 | TTCACCGTGTTAGCC[A/G]GGATGGTCTCGATCT | 115426 |
rs112827787 | snp | G/T | 0.0425829 | 0.139564 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420347 | GGCGTGAGCCACCGC[G/T]CCCGGCCCATTTTTT | 115426 |
rs112834535 | snp | G/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451800 | GTTGTTGTTGTTGTT[G/T]TTGAGACAGAGTCTC | 115426 |
rs112859003 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424129 | TTAGGCAGGAGAACA[A/G]AATAAAGTGTAAATA | 115426 |
rs112915764 | snp | A/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464410 | TTACGATGTTTGAAT[A/T]GTAGTTTTCTTAATT | 115426 |
rs112917458 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481054 | TCTGTAGACGTATAC[C/T]TTGCTTTTTAGAAAA | 115426 |
rs113090944 | snp | A/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424014 | AGGTTAATATTTTAA[A/C]CACATTCTATACCGG | 115426 |
rs113122733 | in-del | -/T | 0.366679 | 0.221102 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446445 | GGCCTAATTTTTTTT[-/T]AATTTTTAGTAGAAG | 115426 |
rs113149326 | snp | A/G | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479633 | ATATTCCTGTATGCA[A/G]TTGGTTAGTTGACTG | 115426 |
rs113162526 | snp | A/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498236 | ATGCCTTAACACTGG[A/T]TATAACCCACAGCAA | 115426 |
rs113310143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480602 | GATATTTAACCTGTG[C/T]ACTAATTTTCTCATC | 115426 |
rs113392041 | snp | C/G | 0.0908922 | 0.192833 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412969 | TAGCCGCGCAATCTT[C/G]CGAAACCCAAAGGCT | 115426 |
rs113405994 | in-del | -/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442652 | CCAGTTAATTTTTGA[-/T]TTTTTTTTTTTTTTG | 115426 |
rs113429734 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490129 | TTGTTTTTAGTGTCT[G/T]AGCAATTGTATTTGA | 115426 |
rs113497867 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493289 | GGTGACAGAGCAAGA[C/T]TCTGTTTAAAAAAAA | 115426 |
rs113506777 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480139 | GTCTCTACCCACCTT[G/T]GTCTTCCTCAAAGCA | 115426 |
rs113575776 | in-del | -/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472886 | AAAAAAGACACATAA[-/T]TTTTTTTAAAAAGTA | 115426 |
rs113583280 | in-del | -/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442477 | TTTTGTTTTGTTTTG[-/T]TTTGTTTTGTTTTGT | 115426 |
rs113626350 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490491 | AAATTACCCAGGCGT[A/G]GTGATGCATGCCTGT | 115426 |
rs113725165 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424011 | AATAGGTTAATATTT[A/T]AAACACATTCTATAC | 115426 |
rs113766395 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498380 | TGGGAAAAGTTGGAC[C/G]TGTTAATTAAAAGTA | 115426 |
rs113814275 | snp | C/T | 0.5 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466778 | TGTGTTGCTTGATCA[C/T]GCAAACATGCTCCTG | 115426 |
rs113879282 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477478 | CTGCAGTGAGCCAAG[A/T]TCACGCCATTGCACT | 115426 |
rs113880101 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506212 | TGTTGTTCATGGTGG[C/T]TTTTTGGACAATAAA | 115426 |
rs113907603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437097 | TCATTCTTTGTGATC[A/G]TTAGAAAAATGAATT | 115426 |
rs113909199 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412160 | TTCCGTCTCTAAATA[A/C]ATACATACATACATA | 115426 |
rs114000144 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433238 | AATACTCCTTCCTTT[G/T]GTCAGATTGCATGGG | 115426 |
rs114002498 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486075 | AATAGATAGGAGCCA[C/T]ATTTAGAGAGGGTAA | 115426 |
rs114049623 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431939 | AATATATGAAACTTA[A/C]ATTTTGATTTGCTGC | 115426 |
rs114246187 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469219 | AAGACCTTGTTAAAT[A/T]GATTTAATAACAAAT | 115426 |
rs114255945 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441574 | TTGACCCAGCCTTAT[C/G]CATTACTATCAGGCA | 115426 |
rs114384498 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491924 | TTTTAATAGAGACAA[G/T]GTCTCGCTATGTCAC | 115426 |
rs114390367 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470096 | ACATTCCCAGCTGGG[A/C]GTGGTGGCTCACGCC | 115426 |
rs114398805 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436744 | TAGAGCACAAAACAC[A/G]GTACCTTAGCATATA | 115426 |
rs114467332 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429815 | TGGTTACACTTAGTG[C/G]GTGATAGATGAAGAA | 115426 |
rs114582739 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431299 | AGTAGGGTACTTACT[A/G]TATTTAGTAGGATAA | 115426 |
rs114675932 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466401 | AAATGTTAGCTGGGC[A/G]TGCTGGTGCACGCCT | 115426 |
rs114678429 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414847 | CTTTAAAATAATGTT[A/G]TAGCACCTTTGATTT | 115426 |
rs114715887 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443900 | AGATTTCTGGAGCTA[A/T]TCTCAGTCTGTGGTA | 115426 |
rs114735927 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473864 | AATGTACAAGAAATG[A/C]GAATGACAGAAAAAA | 115426 |
rs114749020 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479871 | CTCCCAGCCCAAACT[A/G]CCATCTCTTCCTTGA | 115426 |
rs114865613 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442456 | ATTGGCATAAGGTTT[G/T]GTTTTGTTTTGTTTT | 115426 |
rs114880387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438043 | ATCAGGACCTGGTGC[A/G]TGTTCAGAGTAGGAC | 115426 |
rs114887380 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430967 | TAGGCAAATTCTGTT[G/T]TCCTCTTTTGTCTGC | 115426 |
rs114937616 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490656 | AGAATATTATCTTAA[A/T]TATATGAAGTTTATT | 115426 |
rs114996788 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417492 | TTCAATCTTCACTTT[A/C]ATTAAATGTGGAAGA | 115426 |
rs115024110 | snp | A/C/T | 0.0168055 | 0.0901129 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485613 | GTGCCTTTCCACCCC[A/C/T]GCCCCCCGCCCCAAA | 115426 |
rs115119185 | snp | A/C/G | 0.00557925 | 0.0525759 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499780 | CAGGATCTAAACCCC[A/C/G]CTTCTCTGTGAAGCT | 115426 |
rs115120645 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453054 | AAAAATGTATGCTTC[A/G]TTTTCATGACTTACC | 115426 |
rs115174874 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463768 | GAGCCACCGTGTCTG[C/G]AGAAAAAAAATTTTT | 115426 |
rs115208364 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485796 | TGGTGAGACCCCTGT[C/G]TCTACCCAAAAAAAA | 115426 |
rs115251053 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500956 | TTACTTTGAGGTACT[A/G]TTCCTCAGAAGAATT | 115426 |
rs115295378 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448341 | CTTCATTACTTATCT[A/G]TGAATACTATTTAGT | 115426 |
rs115317795 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479897 | CTTGAACTTCTGTAA[C/T]GGATGTCTAACTAGA | 115426 |
rs115420397 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503450 | TGGAGCCAGTAATGG[C/T]TTTTGAAGAATACAG | 115426 |
rs115435650 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443400 | TTAAAGAAGTAACTT[G/T]CTCAGTGTTAGAGAG | 115426 |
rs115446084 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431165 | TGCATCTTGGCCTAT[A/T]CAAATTTTGCTTGAC | 115426 |
rs115553181 | snp | A/G/T | 0.00395355 | 0.0442854 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475543 | CTACATGTGTTGTAC[A/G/T]TGATTGAACTTTATT | 115426 |
rs115581413 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467807 | TCAGGCCTCTGAACC[A/G]GACTGAATCCTAGCT | 115426 |
rs115686021 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467920 | TGTGGTTTATTTCTC[A/G]TTTTAACTGTGAGAA | 115426 |
rs115698679 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446582 | ATCTGGGCACAGTGG[C/G]TTATTCCTGTAATCC | 115426 |
rs115749489 | snp | A/G/T | 0.02016 | 0.0983543 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471530 | TTCCATTTTGGGTGC[A/G/T]CCCTCTTGGATCACT | 115426 |
rs115771149 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458179 | ATTGGTCTCAATTTC[A/G]GAACTTGTTATTGGT | 115426 |
rs115801386 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480424 | TTCTGAACAAACCTG[C/T]TGAAGGAGTGAATCA | 115426 |
rs115809639 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487220 | TTTGAGATGGAGTCT[C/T]GCTATATCACCTGGG | 115426 |
rs115861657 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418200 | TGAATGCAGTGTTTG[C/G]TCCTTGAGTTTTTTG | 115426 |
rs115881405 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452481 | AAAATATTTTAAGTA[A/G]GTCTGTGTCTTAGAA | 115426 |
rs115999043 | snp | C/T | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420088 | TTTTTTGACAGTCTC[C/T]CTCTGTTGCCCAGGT | 115426 |
rs116111801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496886 | CCTTCCCCCAACAAA[C/T]GTTATTTAAAGAAAA | 115426 |
rs116208087 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428228 | ATGTTTAACCTTTTT[A/G]ATTATGAAATGTATT | 115426 |
rs116209760 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485655 | GCTTGAATTCAGTTT[C/T]CTTTACTCTGCTAAG | 115426 |
rs116309856 | snp | C/G/T | 0.0298908 | 0.118541 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420173 | GAGATTCTCTTGCCT[C/G/T]TGCCTCCTGAGTAGT | 115426 |
rs116363148 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416119 | CTGTCGCCAGGCTGG[A/C]GTGGCGCGATCTCGG | 115426 |
rs116549319 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466724 | TGCATATCAAGTTGT[A/G]AGTCACTGGTCACTG | 115426 |
rs116557843 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501830 | ATCAGCCTAATTATT[A/C]TCTGATTGGGAAAGA | 115426 |
rs116586279 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460281 | TGTGGTTCTTGAATG[C/T]GGGCTGAACACTTAC | 115426 |
rs116586816 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UHRF2 | GRCh38.p7 | 9:6505297 | CGTGTGTGTGTGTGT[A/G]TATATATATATATTT | 115426 |
rs116623160 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468211 | TTTATTATGATCAAT[G/T]GCATTTAGTTTTGTG | 115426 |
rs116677937 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453577 | TTGTTATTTTTCTGA[C/G]CAAACCGTTGTGAAA | 115426 |
rs116777321 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449172 | TACTGACCAGCTGCA[A/G]GTAGTGCAGTTAGCT | 115426 |
rs116778827 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443721 | AACCAAATAGGTTCA[A/G]CTGTTACTTTTAATA | 115426 |
rs116779021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488789 | TTACAGGCATGAGCT[A/G]CCGTGCTGAGTGTTT | 115426 |
rs116801368 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425971 | TTTGGCCAGAGTTTA[C/G]AAGCTGCTGCTTTTG | 115426 |
rs116886039 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475229 | AATCACTATGGACTT[C/T]TCCTACTATTGAAAA | 115426 |
rs116956638 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494030 | AGGAGAATTTCAAAC[G/T]GGGAGTTAAAGATCT | 115426 |
rs116959129 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473055 | TCCTAGTACCTAACT[A/G]TGGTCTCGAAATACC | 115426 |
rs117063530 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438605 | TGTAGTTTGAACAAG[C/T]TGTCATTTAGCAAAA | 115426 |
rs117107261 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451947 | GTTAGTTTGGTTTAC[G/T]CTTCTGTTTTAATAA | 115426 |
rs117116498 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453414 | ATTTTCACTTTACAG[C/G]TGAGAAAGGAATATT | 115426 |
rs117192687 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455636 | ATTTTATAGAAGCCA[A/G]TGTGGACTGTTACTG | 115426 |
rs117248924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494146 | TTTCTAGTCTTACTG[A/G]ATACATGTGATATGC | 115426 |
rs117300237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490802 | AAATTTTAGGACTAA[A/G]ATGACATATAGGCCT | 115426 |
rs117385644 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488057 | ACCAGCCTGGGCAAC[A/G]TGGCAAAGCCCTGTC | 115426 |
rs117408110 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463222 | GGAGGCGCAGATTGC[A/C]GTGAGCTGAGGTCAT | 115426 |
rs117420068 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6418080 | TAAAAATAGTCATAA[C/T]GTTTGTCAGTTGTAT | 115426 |
rs117435315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423097 | CCAAAAAATTGGTAG[A/G]TGAAGTAAATTACTC | 115426 |
rs117443648 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441733 | TAGGTGGTTTGTGGC[C/T]GGTTTTTTTTTTCCA | 115426 |
rs117452522 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459758 | GCAGGGGGTTGCTTG[A/G]GGCCAGGAGTTCTAA | 115426 |
rs117579654 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498773 | AGAATTTGTCCCTGA[A/C]ACTGACTTCAGAGCA | 115426 |
rs117597069 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468307 | TGAATTTGTGACATT[C/T]ATTGAATCACTTAAA | 115426 |
rs117615928 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491357 | TGCTGTGAGGTTTAA[A/G]TGAATTAATTATACG | 115426 |
rs117701106 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477025 | CACCTGAGGGGTCAG[A/G]AGTTTGAGACCAGTC | 115426 |
rs117702266 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451135 | GGTAGTTTCAGACTA[A/G]CAATACTTTCATATT | 115426 |
rs117703234 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432449 | TCTTGTCATTTATAT[C/T]AAGGTTCATGGTATG | 115426 |
rs117711633 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455185 | GGGTGCATGTGCACA[A/G]CGAGCTCGTTTGTTA | 115426 |
rs117723061 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452040 | TGTATTTATACATAT[A/G]TACACTAGATAGAAA | 115426 |
rs117750807 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496659 | AGACCTTTAAAGAAC[A/T]TTCTCATACACCACT | 115426 |
rs117776336 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460038 | TTTTTATCACCCTCC[C/T]CAGTCCCCTACTTTC | 115426 |
rs117824474 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429850 | AACCTAGGTTTACCT[A/G]CAGAGCTGGAGTGTT | 115426 |
rs117829702 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6439179 | CTTGGTGAACATAGG[C/T]TGAATTGTTTTTTGT | 115426 |
rs117882882 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492761 | AATTTGTTTCAAGTA[C/T]TGAATCAGATAGAGA | 115426 |
rs117953732 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502412 | AGATTCCTCAGAGAG[A/T]TCTTCCCAAACTACC | 115426 |
rs118010954 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496449 | TAAGCTCATTGATTT[A/C]CTACTATTAGGTGAA | 115426 |
rs118022602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451990 | TATATATGCATTTGT[A/G]TATATGCCATATACC | 115426 |
rs118104905 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461847 | TTTAATAAATAAAAT[A/C]TGTTAATCATTTCCA | 115426 |
rs118114952 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460407 | GGTATCGCAGTACAG[C/G]TGAGAAACCAACATG | 115426 |
rs118131406 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476330 | GTCCAAAGAAAAAGC[C/G]TGTTTCTGTAATTTT | 115426 |
rs118135606 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488807 | GTGCTGAGTGTTTTT[G/T]TTTTGTTTTGTTTTG | 115426 |
rs118166192 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438439 | CTTTAACTAAATAGG[C/T]TTTAAGTGCTTATAG | 115426 |
rs137883549 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415784 | GTTCAGCTCACCCCA[C/G]AACTGCAAGTAGTTG | 115426 |
rs137883601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450780 | GTTTAAAGTGACATA[A/G]TAGTTTTTGAATGTT | 115426 |
rs137906988 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426855 | CTGGGTTCAAGCGAT[A/T]CTACTGCTTCAGTCT | 115426 |
rs137934647 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500309 | TTAAGAAAATAAATT[C/G]AGACTTAAATGAAAG | 115426 |
rs137948215 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447912 | TAGTTTGGAGGAAGG[C/T]ATGTGGAATAGAACT | 115426 |
rs137949462 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453343 | TGCCACTGAAATATG[C/G]TTTTTACAGTGTTAT | 115426 |
rs137951180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480540 | TTCGCTTCACCTGAA[A/C]CTCCTTAACCTTAAA | 115426 |
rs137991560 | snp | C/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6476071 | ATAACCATCATCATT[C/G]TATTCTCCACCTGCA | 115426 |
rs138049601 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503534 | CCTACTGTAAATAAA[C/G]ATTAGCATCAGGAAG | 115426 |
rs138051337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482876 | AGGCATGAGCCACTG[C/T]GCCCGGCCTGGCTTT | 115426 |
rs138056538 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430193 | TTTTGTACTTTTAGT[A/G]GAGACAGGGTTTCGC | 115426 |
rs138065649 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451004 | TATTGATAGTTCCAA[C/T]TAAATTTAGAGGAGG | 115426 |
rs138123864 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481050 | TCATTCTGTAGACGT[A/G]TACCTTGCTTTTTAG | 115426 |
rs138126510 | snp | C/T | 0.000280114 | 0.0118313 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460648 | CATTTTGAAATGGAA[C/T]GAACTAAATGTTGGT | 115426 |
rs138163072 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459008 | CACTCATAAGTGGAA[A/G]TTGAACAATGAGAAC | 115426 |
rs138187099 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437796 | CTAATGTTTGTATTT[C/T]TAGTTGAGACTGGGT | 115426 |
rs138215892 | in-del | -/A | | | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412272 | GGCGGGGTGGGGGGT[-/A]GGGGGAAGCCCTGTT | 115426 |
rs138282715 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414819 | AGAGCTTTTTTTTCC[A/C]CTTTCCTTCTCTCTT | 115426 |
rs138303091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442335 | TCTTCCCTGATTGTA[A/G]AATGCTTTTCCTTGA | 115426 |
rs138330569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459147 | GGTGCAGCAAACCAC[C/T]GTGGCACCTGTATAC | 115426 |
rs138339837 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466314 | AGGCTGAGGCGGACG[A/G]ATCACCTGAAGTCAG | 115426 |
rs138370843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422025 | ATCTGGGCTGTTTCC[A/G]GTTTCATCTGTTTTA | 115426 |
rs138440863 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462990 | TTAGAAGTGGAACTG[A/C]GACTGAGTGGGCCAG | 115426 |
rs138442051 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6495145 | AATAATCGATAATTT[A/T]GCTTGAAAGGAACTT | 115426 |
rs138465203 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500927 | ATTTTGACTTCTCTA[A/T]GCCCAAAGTTACTTT | 115426 |
rs138479589 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491765 | TCCCTTGTGCAGATA[G/T]AGCTGCTTTATGTGA | 115426 |
rs138518717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6419010 | TTCACATTGTCTTCC[A/G]GCTGCATCTTTCCAA | 115426 |
rs138551615 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502369 | TTCATGTGTCTCACT[C/G]TTTCATATCCTTTAA | 115426 |
rs138563954 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430098 | CCATTACAACCTCCA[C/T]CTCCTGGGTTCAAGT | 115426 |
rs138601485 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480776 | TCATAGTATTTAGTG[C/T]CTTCTCAAACATAAT | 115426 |
rs138620600 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487133 | ATGTGTTTGTTAAGT[C/G]ATTATTATAAGGAAA | 115426 |
rs138651742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427377 | GGCATAGGTAAACAT[G/T]TAAACAGTATGTTAA | 115426 |
rs138655225 | in-del | -/TTTGTTTTG | 0.095934 | 0.196885 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442469 | TTTGTTTTGTTTTGT[-/TTTGTTTTG]TTTGTTTTGTTTTGT | 115426 |
rs138665792 | snp | A/G | 0.00119649 | 0.0244297 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6499894 | AGGACAGTCAAAGAA[A/G]CAGCCCAGTGGAACC | 115426 |
rs138700713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479325 | AGTTCTCATTCCTTA[A/C]TCAACTGCTTAGCTG | 115426 |
rs138712647 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434014 | GACAGTCACGTGGCA[A/C]AACTCCACTGAAGAA | 115426 |
rs138753804 | snp | C/G | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507271 | AGATGGAGTCTTGCT[C/G]TGTTGCCTAGGCTGG | 115426 |
rs138754604 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6462428 | CTATTGCTAGACTAA[G/T]GGTATAGCTCAGTCA | 115426 |
rs138813672 | in-del | -/TTTG | 0.0926964 | 0.194308 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455131 | CAGCTTTTTTGTTTG[-/TTTG]TTTGTTTGTTTATAC | 115426 |
rs138880844 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491592 | AGTCTATAGGGAGGA[A/G]GCTGAGAAGTTTGGG | 115426 |
rs138886283 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442063 | CTCTGCCTCCTGGGT[A/T]CAACAATTCTCATGC | 115426 |
rs138889673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432771 | TGATTTCATTTTTTC[C/T]TTTTTAAGGGCTTAA | 115426 |
rs138942307 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466694 | CATGGCTTCTTACAG[A/G]ATATATACTTAATAT | 115426 |
rs138951468 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430508 | ACTGCCCTTTTTCCT[A/G]GAGCTAGCTTATTCC | 115426 |
rs138952938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6495712 | TTGTTGCTGTATTGC[C/T]TAGTTTCATCCTCTT | 115426 |
rs138975847 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489619 | ATTCTGATAGGTGTG[G/T]GTTGATATCTTATTG | 115426 |
rs138981680 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437997 | TACTAGGAATATTGT[A/C]CTCCAGCTCTCATGC | 115426 |
rs139055222 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6435660 | CACCCAGGCTGGAGT[A/T]CAGTGGTGCGATCTT | 115426 |
rs139066957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487931 | AGATAGTTGTAGATT[A/C]ACGTGTAGCATTAGA | 115426 |
rs139073908 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487313 | CCTGCCTCAGCCTCC[C/T]AAGTATGTGAGATTT | 115426 |
rs139097155 | in-del | -/AAAT | 0.306431 | 0.243548 | intron-variant | UHRF2 | GRCh38.p7 | 9:6423949 | ACTCAGTATCAAAAA[-/AAAT]AAATAAATAAATAAA | 115426 |
rs139105809 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419892 | CCACAGGCATGTACA[A/G]TCACACCCGGCTACG | 115426 |
rs139193480 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468226 | GGCATTTAGTTTTGT[A/G]CATAAAGAGTGTCTT | 115426 |
rs139202850 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497424 | AAGGCAGGGTTGTTG[C/T]AAGGAACTACTGTGG | 115426 |
rs139211049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425158 | AGTTAATGTACTTCA[C/T]TGCCTTGAGGGCAGA | 115426 |
rs139269809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481234 | AACTACCATTTTTCT[C/G]TGGGAATTCTAATAA | 115426 |
rs139304250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447250 | AAATAGATGTCAGGC[A/G]GTCATACTTTATTAT | 115426 |
rs139318155 | in-del | -/AACAA | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6424125 | GCAATTAGGCAGGAG[-/AACAA]AATAAAGTGTAAATA | 115426 |
rs139343787 | snp | C/G/T | 0.00835779 | 0.0641761 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484177 | CTGGGCTCAAGTGAT[C/G/T]ATTCCACCTAGCTAG | 115426 |
rs139370657 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445601 | CTTACTGTGTCACAC[A/T]GGTTGGAGTGCAGTG | 115426 |
rs139374616 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6431067 | GGATCTTCTGTGTTC[A/G]TATTAATCATACAGG | 115426 |
rs139374708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478784 | TTGGGAAGGCAATTG[C/T]TGTATTATGACAGGC | 115426 |
rs139410455 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448731 | AAATAAGATAAGAAT[A/G]GAAAGTTTTCGCCTC | 115426 |
rs139418295 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479421 | CTTCTTAGTCTCTTG[C/T]TGGGTTCCCGTCACC | 115426 |
rs139486821 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501646 | GATACATTGAGTTAT[C/G]TTTGGCAAAATGAAG | 115426 |
rs139511005 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490276 | ATTAACTGAGATAAT[G/T]TATGTGGCCCTTTGC | 115426 |
rs139523629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448415 | TAATATGTTCAAGAA[C/G]AAGAAAAAGTTTGTC | 115426 |
rs139547211 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496310 | CTTAAGACGTAGGTG[C/T]CCTAGAGGAAAATGC | 115426 |
rs139561574 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493010 | TGTTAGAATTTTAAT[A/G]TGAAAGCCAGGGCGC | 115426 |
rs139571836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443108 | ATGTAAAGAAGGAAA[A/G]TTCTTATGAAAGTTA | 115426 |
rs139621444 | in-del | -/C | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6416535 | GGTGGATCTCTAAAT[-/C]TTTTTTTTTTTTTTT | 115426 |
rs139710116 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454367 | AATTAGGAAAGATGA[A/T]GATTGAGGCTGGCAG | 115426 |
rs139755411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460261 | GCTCCCTCAAAGTAG[A/G]TGATTGTGGTTCTTG | 115426 |
rs139826797 | snp | C/G | 0.000124134 | 0.0078773 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460802 | CTGGGGTAAGATTGT[C/G]TTCACTGGTGCCATT | 115426 |
rs139909256 | snp | C/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6427697 | CTCAAAAAAAAGAAA[C/T]TTTAATCTGAAGTTA | 115426 |
rs139912167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6457988 | TTTGTTGTGTCTCTG[C/T]CAGGTTTTGGTATCA | 115426 |
rs139971005 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476505 | TACCTCTTCATTTAA[C/T]GGATTTTTCTTACTT | 115426 |
rs139973822 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487595 | TGGTCTCGAACTCCT[A/G]ACCTCAGGTGATCCT | 115426 |
rs139975960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472461 | AAACTAGCCTTTAGT[A/G]TAACAGCTATAGACA | 115426 |
rs139976155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425436 | AATCAACCATTTCTC[C/T]AAGGTTCCCTGTTTC | 115426 |
rs139980843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417135 | CCTAGTCAGTAGTTG[C/T]TTGGGAATGACTTCC | 115426 |
rs139989550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454532 | TACGTGAACACAGAG[C/T]GGCTTTTCTTAGAGT | 115426 |
rs140009163 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6477318 | TCACCTGAGGTTGGA[A/T]GTTTGAGACCAGCCT | 115426 |
rs140046599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504532 | ATACACAGTAGATGA[A/G]TTTTATTAGCATATT | 115426 |
rs140076470 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477660 | CTGTGTGGTGGAGAC[C/T]CAGAAAAGAAATGTC | 115426 |
rs140156631 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434687 | CAAGTGATCTGCCCC[C/G]CTTGGCCTCCCAAAG | 115426 |
rs140168343 | in-del | -/TT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6467616 | TTCCGAGAGAATAGT[-/TT]TTTTTTTTTTTTTTT | 115426 |
rs140189289 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463108 | CCAACTAGTGAAACC[C/T]TGTCTCCACTAAAAA | 115426 |
rs140189468 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6431364 | TGTAATCTCAGCACT[A/G]TGAGAGACCAAGGAA | 115426 |
rs140267584 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458379 | CTATTTGGTTCTTCT[C/T]TCTTTTCTTCTATGT | 115426 |
rs140278518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485691 | TTGTATTGGCCAGGC[A/G]TGGTGGCTCACACCA | 115426 |
rs140312864 | snp | A/C/G | 0.0146672 | 0.084371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482826 | TGGTCTCGATCTCCT[A/C/G]ACCTCGTGATCCACC | 115426 |
rs140334597 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442697 | GGGTCTCACTTTGTT[G/T]CCCAGGCTGGTCTCG | 115426 |
rs140392065 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414426 | CGTTCACGCTTTAAG[C/G]ATAGCACTGCAGCAT | 115426 |
rs140401964 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6471085 | ATTGTAAGAAGATGA[C/G]AACAGCAAAGACTTT | 115426 |
rs140414264 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467436 | TTATAGGTTCCTGGA[A/G]TTAGGACATGAACCT | 115426 |
rs140418740 | in-del | -/AAGGA | 0.0614824 | 0.164198 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469030 | ATAATCAGAAAACAG[-/AAGGA]AAGGAATACCAATTA | 115426 |
rs140543061 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414583 | CGTATTTTTCTTTGT[C/G]TTCATGTTGTTGTTA | 115426 |
rs140591990 | snp | A/G/T | 0.0006669 | 0.0182489 | intron-variant | UHRF2 | GRCh38.p7 | 9:6493815 | TTAATAAAGAAAATC[A/G/T]TCTCTGACAGGACCG | 115426 |
rs140599456 | snp | C/G | 0.00553074 | 0.0522951 | intron-variant | UHRF2 | GRCh38.p7 | 9:6497997 | TAAATCTCAAACTGG[C/G]ACTGAAATATTGTGA | 115426 |
rs140612271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6426000 | TGAATTGATTGTTTG[A/G]GCATTGACAGGATGG | 115426 |
rs140636762 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494975 | AAAACATTCTTGAGA[A/C/T]AGGAGCTTAGCTATT | 115426 |
rs140643038 | snp | A/G | 2.06601e-05 | 0.00321397 | intron-variant | UHRF2 | GRCh38.p7 | 9:6499788 | AAACCCCCCTTCTCT[A/G]TGAAGCTTAAATCTG | 115426 |
rs140669641 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482697 | TGCCTCGTGGGTTCA[C/T]GCCATTCTCCTGCCT | 115426 |
rs140727862 | snp | A/G | 0.0146024 | 0.08419 | missense, nc-transcript-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6421105 | CATCTACATCAGCTC[A/G]TGCCCGTCTTATTGA | 115426 |
rs140768955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430647 | CCAATATTCCGCCCT[A/G]ATCACCCACAGCCAG | 115426 |
rs140812543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6486392 | GGGCTAAAATAACTC[C/T]TGCATTTTTGACTTC | 115426 |
rs140815214 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6432666 | ATTTAACTTACTTCT[C/G]CCACGAGGTATGCCA | 115426 |
rs140825731 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429060 | ATCCCAGCTACTCAG[G/T]AGGCTGAAGCAGGAG | 115426 |
rs140828639 | snp | C/T | 0.000184913 | 0.00961365 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481621 | TTGTGAAAATGCCTT[C/T]GTTCTTTTTTTTCTT | 115426 |
rs140835054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428444 | TTAACCTTTAACAAC[C/G]TATTAATAATCTTTA | 115426 |
rs140892418 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458226 | CTTCTTCCTGGTTTC[A/G]TCTTGGGAGGGTGTA | 115426 |
rs140919014 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461957 | GATTTGTTTTATTGA[C/G]TGCCGAGGGTTTTAG | 115426 |
rs140977224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491294 | TTTTAGGCGATTTAC[C/T]GAACCTCTGCCACAT | 115426 |
rs141015510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501806 | TTAAGATACAGGAAG[C/G]AGTTGTTAATCAGCC | 115426 |
rs141090109 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478868 | CTACTACCTCATATG[A/G]TCACACTCTGAATTT | 115426 |
rs141100200 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6452355 | AGACAGTGTTTCTGG[C/T]AATTAACAGATGCCC | 115426 |
rs141162725 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492644 | TAGACACAAAACATC[A/G]TTGTCTAAGTTGTCT | 115426 |
rs141188929 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6504596 | ATACTGTTCTAGAAT[C/T]TTCTGAAAAAATTGG | 115426 |
rs141195427 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419722 | GTCACAGCCACAATG[A/C]AACATTTTGGGATTT | 115426 |
rs141227343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6502773 | ACTGTGGAAGTACCA[A/G]GTTAAATATTGGTCA | 115426 |
rs141229947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450950 | GTCTTTTCGTTGGAA[A/G]AGAACTAGGAAATAA | 115426 |
rs141290225 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473657 | GCCCAGGAGTTGGCA[A/G]TATTTTTCTTCTGTA | 115426 |
rs141293069 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441798 | AATTCTTTTCTAAAA[A/T]TATATTTCATTCAAG | 115426 |
rs141300134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6468937 | GGAAGGTTGAACTTT[C/G]CTTTATATAAGATAA | 115426 |
rs141305708 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490489 | AAAAATTACCCAGGC[A/G]TGGTGATGCATGCCT | 115426 |
rs141360350 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440728 | TTGTATATAAAAAGC[A/G]TCTGCTTTCAGTGGA | 115426 |
rs141431937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437354 | TCTCCTGCCTCAGCC[G/T]CATGAGTACCTGGGA | 115426 |
rs141490017 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487231 | GTCTCGCTATATCAC[C/T]TGGGCTGGAGTGCAG | 115426 |
rs141492382 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430725 | TTATTCAAACTAGCC[A/G]TCTTGTTTCCCCTGC | 115426 |
rs141501608 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460127 | TCAAATCATGAGTGT[A/G]TATCATTTAAGTGCC | 115426 |
rs141502090 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489088 | GTGCTGGGATTACAG[A/G]CGTGAGCCACTGCTC | 115426 |
rs141570758 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415382 | ATAGACCTTTGGTGC[C/T]AGCCATTAACTTGGA | 115426 |
rs141662474 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421462 | CTGTCACCCAGGCTG[G/T]AGTGCAGTGGCGCAC | 115426 |
rs141701241 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480857 | TCAACAAAGTATCTC[A/G]TAATTGGATTGACTT | 115426 |
rs141707244 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479150 | CTGGCTGCCTACCCC[A/G]TTCTCTGCTTCTTTC | 115426 |
rs141713342 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427394 | AAACAGTATGTTAAG[A/G]TGAAATTTTAGGCCA | 115426 |
rs141724018 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506101 | GCATGATCTTGGCCA[A/G]AATTACATCATGATT | 115426 |
rs141769348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479377 | GAGATCAGGTAATCC[C/T]GATTTTCTACCTACT | 115426 |
rs141807496 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6481080 | GAAAAGATTCAAGGC[A/G]GTTTACGAAATACAA | 115426 |
rs141819709 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483604 | TGTGGGCCAACTGTA[A/C]TACATAAAAATGGCT | 115426 |
rs141831269 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | UHRF2 | GRCh38.p7 | 9:6424163 | GAGAAGGCAAAGTTG[C/G]AGCCTATGGATACCT | 115426 |
rs141847006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450558 | TTTCTGTGGTAAGAT[G/T]CAGGTGTTGTCAGCC | 115426 |
rs141886837 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507274 | TGGAGTCTTGCTCTG[C/T]TGCCTAGGCTGGAGT | 115426 |
rs141918107 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6502391 | ATCCTTTAAGTCTGT[A/G]TAAATAGATTCCTCA | 115426 |
rs142001985 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445589 | TTGAGACAGGGTCTT[A/G]CTGTGTCACACAGGT | 115426 |
rs142025293 | in-del | -/TG | 0.0528381 | 0.153711 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474033 | AAACACAGGCAAAAC[-/TG]TTTTAGGGAGGTAGA | 115426 |
rs142039669 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463143 | AAAATTAGCTGGGTG[C/G]GGTGTTGCATGCCTG | 115426 |
rs142105495 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6491593 | GTCTATAGGGAGGAG[A/G]CTGAGAAGTTTGGGA | 115426 |
rs142146005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414357 | TTATTCCCGAAGTGA[A/G]AAGGAGTGTAAGACT | 115426 |
rs142163039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489895 | GGCTTTCTGAAAGGC[A/G]GATTTGGCAGTGCAT | 115426 |
rs142165376 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6488587 | AATCTTGCCCTTGTC[A/G]CCCAGCTTGGAGTGC | 115426 |
rs142173463 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496612 | ACAGGCATTTGGATG[C/T]TTCAGGCTTATTGAA | 115426 |
rs142177972 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446296 | GATGGAATTACAGGC[A/G]TGTGCAACCACACTT | 115426 |
rs142234499 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478173 | TCCTCTTTCATTTCC[C/G]CAAATACTCTACACT | 115426 |
rs142313225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490621 | TGACAAAGTGAGACT[C/G]TGTCTTTAAAAAGAA | 115426 |
rs142322089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421359 | GAGCAATAAAGGAAA[A/T]ACTTGTGTAATTGCA | 115426 |
rs142365578 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504392 | GATGGATATATTTTG[G/T]GATACATGTGAAATT | 115426 |
rs142417073 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425843 | TCATTGCTTTTAGAG[A/C]CTTCAACAGACAGCA | 115426 |
rs142457461 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422919 | ATAGAGAAATGAAAT[C/T]GATTTATTTGGCTTT | 115426 |
rs142490319 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438825 | GAATTAGGCCAAGAT[A/C]AATAGCTATTCTCTT | 115426 |
rs142510946 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480228 | CTTTTCTTAGGTTAT[C/G]TACTGTAAGAAGCAT | 115426 |
rs142519970 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6506893 | ACTTCTCTACTAGTC[A/G]AACTGCTTTTAGTGT | 115426 |
rs142523112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453676 | GGGATTGGCCAAGGC[A/G]GGCAGATCACGGGGT | 115426 |
rs142526785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6420155 | TCCACCTCTGGAGTT[C/G]AAGAGATTCTCTTGC | 115426 |
rs142566043 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425788 | TAAAAAAAAAAAAAT[C/G]AAGATCTCGGCTCTA | 115426 |
rs142585094 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6503655 | GTTTCCTAGTGTTTT[C/T]TTTTAAGCTCCTAAA | 115426 |
rs142594580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443149 | ATCTGATCTTAAGAA[C/T]GAAGCTACCTTTGGC | 115426 |
rs142615603 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6461324 | TTCTTTTTTTCTTTC[C/T]GTCTCTCTCCCTCCC | 115426 |
rs142627098 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | UHRF2 | GRCh38.p7 | 9:6472104 | AATGTTTTCATCACT[C/G]CCAAAAGTTCCCTTG | 115426 |
rs142630358 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | UHRF2 | GRCh38.p7 | 9:6421575 | ACGTGCACCACCACG[A/C]CCGGCTAATTTTTGT | 115426 |
rs142647179 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451389 | TCTGTAGTTAAATCT[C/G]CAAAACAAAATATAC | 115426 |
rs142669690 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504803 | CGGGATAGTTGCGGA[A/G/T]CCTTCTAGTTAAGAA | 115426 |
rs142677414 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445631 | GGCACAACCACAGCT[C/G]ACTGCAACCTTGACC | 115426 |
rs142739079 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6475872 | ACATTCTATCATTTT[G/T]TGTGTGTGTTGGGAA | 115426 |
rs142760639 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504192 | CGCCACGCCCAGATA[A/G]TTTTTTGTATTTTTA | 115426 |
rs142772533 | snp | A/C | 9.9054e-05 | 0.00703685 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | UHRF2 | GRCh38.p7 | 9:6434088 | TCCAAAGAGAACACA[A/C]ATAAATTGGACAGTG | 115426 |
rs142780701 | snp | C/T | 1.69272e-05 | 0.00290918 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460786 | TCGTGTGAAAATTTT[C/T]CTGGGGTAAGATTGT | 115426 |
rs142818369 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6449294 | TGTGACAGTGCTTCT[A/G]GATTTGGCAATTTCT | 115426 |
rs142854351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6437907 | GTGAGCCACCGCACC[C/T]GGCTAGTTTCATTAG | 115426 |
rs142882885 | in-del | -/T | 0.0410537 | 0.137264 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450914 | TGCTGCTTACTGATA[-/T]GTGTTTGGTCATGTT | 115426 |
rs142898618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433149 | TGATCTTTTAAACAG[C/T]GTTTAAAAGGAGAGG | 115426 |
rs142920195 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466353 | GACCAACCTGGGCAA[C/T]GTGGTGAAACGCCAT | 115426 |
rs142920247 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434525 | CTCACTGCAACCTCA[C/G]CCTCCTGGGTTTAAG | 115426 |
rs142957053 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456822 | TGTTTTTGTCAGGAT[C/T]GTCAAAGATCAGATA | 115426 |
rs142993712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482572 | ATTACAGACACCCAG[A/G]ATTCTGAATATTAAA | 115426 |
rs142995711 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6428652 | CCTTCTGGGCTTAAG[C/T]GATCCTGCTGCCTCA | 115426 |
rs143032305 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450866 | AATCCCAGTTATTTC[A/G]AATTGGAAATGGTAT | 115426 |
rs143037654 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | UHRF2 | GRCh38.p7 | 9:6463079 | CTGAGGTCAGGAGAT[C/G]GAGACCAGTCTGACC | 115426 |
rs143087618 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6487334 | TGTGAGATTTCAGGC[A/G]CCTGCCATCACACCT | 115426 |
rs143152401 | snp | A/G | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6483923 | CGAACTCCCAACCTC[A/G]GGTGATCTGCCTGTC | 115426 |
rs143160669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485411 | TATGAGGTTGTTTTC[A/C]TGAGCATCTAGTGAG | 115426 |
rs143172497 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | UHRF2 | GRCh38.p7 | 9:6483444 | AATACCTAATAAAGT[A/G]TAAATGCTATGTAAA | 115426 |
rs143234570 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6465284 | ATGCGTGAAATTTAC[A/C]TGTTAATTTTCCTAT | 115426 |
rs143243762 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | UHRF2 | GRCh38.p7 | 9:6494579 | TAATTTCAAAATGTT[G/T]TATTTTATAAATGCA | 115426 |
rs143316194 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6414978 | ATACTACATAGATTT[A/G]CTTTGCTGTGCCTCA | 115426 |
rs143318881 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447268 | CATACTTTATTATAT[A/G]TTTGATTAAGACCTT | 115426 |
rs143342836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498695 | ACCCATAAAGACTTC[A/G]TTGATTTTGTGTGCA | 115426 |
rs143348472 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6447181 | GGCATGAGCCACCGC[A/G]CCCAGCCAGCACACG | 115426 |
rs143380400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6470180 | GAATTCAAGACCAGC[C/T]TGGCCAACATGGCAA | 115426 |
rs143388858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6415889 | CTAGTCTCTTACTAT[C/T]CAAAGTATGGTCCCT | 115426 |
rs143438612 | snp | A/G | 1.88535e-05 | 0.00307024 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500749 | TAACATTCTGATATT[A/G]ACAAATGATAAATAA | 115426 |
rs143451187 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479045 | TAATTCCTCTCCCAC[A/G]TTGCCATTACTAGAT | 115426 |
rs143455142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6422510 | ATCTGATGGGATTCT[A/G]TGGAGATTGCATCTA | 115426 |
rs143518610 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476797 | ACGGGGTTTCACTGT[G/T]TTGGCCAGGTTGGTC | 115426 |
rs143539223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446609 | ATCCCAGCAGTTTGG[A/G]AGGCCAAGGCGGGTG | 115426 |
rs143552417 | in-del | -/TTTT | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6492833 | GGAGAGCTTTTGGCT[-/TTTT]TTTTTTTTTTTTTTT | 115426 |
rs143559897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6496320 | AGGTGTCCTAGAGGA[A/G]AATGCTAATTTTAAA | 115426 |
rs143617653 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6456721 | TATATAAGGTGTAAG[A/G]AAAGGGTCCAGTTTC | 115426 |
rs143630983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441645 | ATGACAGTTTAACTA[A/C]ATATATTTTAAAGAC | 115426 |
rs143697277 | snp | A/G | 6.5912e-05 | 0.00574035 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6477691 | ATTCTTGCTCCTGTC[A/G]TGTATGTGGTGGGAA | 115426 |
rs143763700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6445279 | TATGTATTGATTGAT[G/T]GATTGATGGAGTCTT | 115426 |
rs143769886 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474509 | TCAGGAGTTCGAGAC[A/G]AGCCCAGCCAACATG | 115426 |
rs143779364 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6459074 | GCCTGTCGGAGGGTA[C/G]GGGGCTAGGGGAAGG | 115426 |
rs143802216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6430551 | ACAGCTGATCAGTGA[A/G]CCTGCCTTTTATATA | 115426 |
rs143852538 | snp | A/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445130 | ACCCTATCTCTTATT[A/T]AAAAAAAAAAAAAAA | 115426 |
rs143865484 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6492165 | TAATGGTACAGAATT[G/T]TAGCCATGTTTCCTT | 115426 |
rs143868795 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442539 | ATTGAAATGCAGTGG[C/T]ACAAACATGGCTCAC | 115426 |
rs143948077 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UHRF2 | GRCh38.p7 | 9:6434705 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGGGT | 115426 |
rs143953841 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6458161 | TTTTGGTTGGAACTT[A/G]TTATTGGTCTCAATT | 115426 |
rs143957621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6490150 | TTGTATTTGATCTGG[C/T]CTCTGACATTTGTTG | 115426 |
rs143998817 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6488127 | ATGTGCCTGTAGTCC[C/T]GGCTACCCAGGAGGA | 115426 |
rs144042427 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6476436 | TTGAGCCTTGAATTT[C/T]TGGGAGGTAATAAAT | 115426 |
rs144100532 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6419278 | ATAAGGTCACATTCT[C/G]AAGTACCATGGATTA | 115426 |
rs144139121 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417065 | AACATATATAATACA[C/T]ACATATATAATATGT | 115426 |
rs144149550 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474823 | TCTGACAAGTATGGT[A/G]TAGTATTTGAAAGAC | 115426 |
rs144169243 | snp | A/G | 0.00060955 | 0.0174472 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | UHRF2 | GRCh38.p7 | 9:6460667 | CTAAATGTTGGTGAT[A/G]TGGTAATGGTTAATT | 115426 |
rs144171766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6448952 | TCTTTAAACATCGCA[A/G]AACAAGCAGTATCAT | 115426 |
rs144177616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473255 | GATAAGAAAAATAAA[A/G]TGGGTTGAGACATAC | 115426 |
rs144179939 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6417298 | TCCTAACCATTTTTG[C/T]TTCTTAAGTATTGTA | 115426 |
rs144210722 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6501745 | ACACCCAGGCGTAAG[C/T]AGAGTCTGACTTTGT | 115426 |
rs144254539 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6504255 | TGGTGTCGATCTCCT[A/G]ACCTTGTGATCCGCC | 115426 |
rs144281515 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6442722 | GTCTCGAACTCCAGG[C/G]TCAAGCAATCCTTTC | 115426 |
rs144326753 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UHRF2 | GRCh38.p7 | 9:6498215 | ATATACACCTCTTCT[A/G]TCTACATGCCTTAAC | 115426 |
rs144328650 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6489405 | TTGTAAACGTAAGTC[C/T]TTATTTCTTTGGAAT | 115426 |
rs144350600 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6440308 | ATAACTTCTTACACA[A/G]ATGCTATGTAATATT | 115426 |
rs144363786 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6467774 | TGAGCCTTTTTAGAC[C/G]ACATAGGTAGCATGA | 115426 |
rs144379455 | snp | G/T | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6442482 | GTTTTGTTTTGTTTG[G/T]TTTGTTTTGTTTTTG | 115426 |
rs144429595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6464813 | CATAATACAACAGAG[C/T]ACATGATCCTGCCTT | 115426 |
rs144434027 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6466854 | TTTGACTTACTCTGT[C/G]TCTTATTTCAGTTCT | 115426 |
rs144543405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6416993 | TTTTCACACAGAATA[A/T]AAAAGTACTTGCCTA | 115426 |
rs144549205 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UHRF2 | GRCh38.p7 | 9:6460277 | TGATTGTGGTTCTTG[A/C]ATGCGGGCTGAACAC | 115426 |
rs144574538 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UHRF2 | GRCh38.p7 | 9:6500983 | AATTTTCAGTTTGTG[A/G]AACATCGTCATTTTA | 115426 |
rs144608943 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UHRF2 | GRCh38.p7 | 9:6482797 | GAGACGAGGTTTCAC[C/T]GTGTTAGCCAGGATG | 115426 |
rs144616269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6429287 | GCAAATGTATTTCAT[A/G]TCTGGACCTCATTAG | 115426 |
rs144683111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6425429 | GTCCTAGAATCAACC[A/G]TTTCTCCAAGGTTCC | 115426 |
rs144698227 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454384 | ATTGAGGCTGGCAGG[C/G]ACATTTAGGCTAAGT | 115426 |
rs144703013 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6479712 | TAAAATCCTGCTCCT[A/C]CCCCAGTCTTCATTA | 115426 |
rs144704863 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6427235 | TACATGTAGAGCTTT[C/G]TATAGTTGAAATTGC | 115426 |
rs144709222 | snp | C/T | 0.00795532 | 0.062565 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507531 | AGGCATGAGCCACCG[C/T]ACTCGGCCCTCAGTT | 115426 |
rs144746395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6433675 | TCAGTAAGGCGTAAA[G/T]AAAACACCTATTTCA | 115426 |
rs144762218 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UHRF2 | GRCh38.p7 | 9:6451888 | TCCCTGGGTTCAAGC[C/G]ATTCTCCTGCCTCAG | 115426 |
rs144774418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6450132 | TACAAAGTGTAACAA[A/C]AAATGTCACATAAAA | 115426 |
rs144776908 | snp | G/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6481715 | CAAGATGAGTAAAAA[G/T]AAAGCAAAGATGCCG | 115426 |
rs144781648 | snp | C/G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6507201 | ACCAGAATGAAATCT[C/G/T]AAGCACTCAGAACAA | 115426 |
rs144825040 | snp | A/T | 0 | 0 | intron-variant | UHRF2 | GRCh38.p7 | 9:6438332 | GCACTGCAAAGAGAA[A/T]CTATGAAGTTAGTAA | 115426 |
rs144840257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6480274 | TCTTGTCACATATAA[C/T]CCTGATGTATTTCCA | 115426 |
rs144889864 | in-del | -/C/CC | | | intron-variant | UHRF2 | GRCh38.p7 | 9:6445966 | TTGGTAAATACTCTT[-/C/CC]TCCCCCCCCGCCACC | 115426 |
rs144929699 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6436176 | TTATTTTTCATACCA[C/G]AAAACAGTATAACAA | 115426 |
rs145004076 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6444457 | TCTTCAAACTTATAT[A/T]TCGTCCCTTTACATT | 115426 |
rs145053137 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441347 | CCATTGTACTCCAGC[G/T]TGGGTGACACGGTGA | 115426 |
rs145069988 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UHRF2 | GRCh38.p7 | 9:6473926 | TCAAAAATCAACACT[A/G]TGAGAAACACTATAG | 115426 |
rs145070081 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441940 | TTGTCTGTTAAATTC[G/T]TGAGTGGGGGAAATA | 115426 |
rs145082637 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6474436 | ATGGGCTGGGTGTGG[-/T]AACTCATGCCTGTAA | 115426 |
rs145104485 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UHRF2 | GRCh38.p7 | 9:6469140 | ACATGGTGAATTTCA[G/T]CTGAGAATTGGAATT | 115426 |
rs145113174 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UHRF2 | GRCh38.p7 | 9:6412356 | GGAGTTCTTTCTTCG[G/T]AGGCGCGTAGCTCTG | 115426 |
rs145148945 | in-del | -/C | 0.0193772 | 0.0965046 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485544 | TTTCAAAAGCCAAAA[-/C]CTTTCCAGGTTCTGT | 115426 |
rs145175600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6443937 | TTTGAGTAGCCTTAA[C/T]TGTGGCTACTGCAAA | 115426 |
rs145254677 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UHRF2 | GRCh38.p7 | 9:6441158 | CCAAGGCAGGTGGAT[C/T]ACTTGAGCCCAGGAG | 115426 |
rs145262744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6455638 | TTTATAGAAGCCAGT[A/G]TGGACTGTTACTGAT | 115426 |
rs145329042 | snp | C/T | 0.252421 | 0.249988 | intron-variant | UHRF2 | GRCh38.p7 | 9:6446919 | TTTGAGACAGAGTCT[C/T]GCTCTGTCACCCAGG | 115426 |
rs145372975 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UHRF2 | GRCh38.p7 | 9:6478152 | CAGCAGTATCTCTTA[C/T]CACTTTCCTCTTTCA | 115426 |
rs145373662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UHRF2 | GRCh38.p7 | 9:6485954 | ATGAGGGGAAAAGCC[A/G]TCATCCATTGAAGTA | 115426 |
rs145378878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UHRF2 | GRCh38.p7 | 9:6454831 | AAATACTAATTCCTG[C/T]ATTTCTATGGCACAG | 115426 |
rs145379225 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | UHRF2 | GRCh38.p7 | 9:6453305 | TAATTTTGACAGAGT[A/T]AGGTTAATGGAGGTG | 115426 |
rs145384660 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UHRF2 | GRCh38.p7 | 9:6484942 | GGTATTACAGGTATA[C/T]GTCACCATGCCCAGC | 115426 |
rs145394234 | snp | A/G | 0.000235988 | 0.0108599 | synonymous-codon, nc-transcript-variant | UHRF2 | GRCh38.p7 | 9:6486916 | GGCTGGTGGATTTGC[A/G]GATGAAGTCGTAAGT | 115426 |