SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12830 | snp | A/G | 0.43608 | 0.166955 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35013777 | TGATGCAGAATCTTC[A/G]TTTTCATTAAATATG | 8453 |
rs15460 | snp | C/T | 0.4422 | 0.159872 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009984 | NNNNNNNNAATGTAT[C/T]TTAAAGGACATAAAA | 8453 |
rs998658 | snp | A/G | 0.46845 | 0.121572 | intron-variant | CUL2 | GRCh38.p7 | 10:35119726 | CAGACATGCTACCAC[A/G]TCTGGCTCATTTTTC | 8453 |
rs1131510 | snp | A/G | 0.0633504 | 0.166319 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010157 | TGCCACGTCATGAGC[A/G]TCAAAGAAAATGCCT | 8453 |
rs1131511 | snp | A/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010121 | TATTTCAAGCTCATG[A/T]CATTATGACATTTCT | 8453 |
rs1213387 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | CUL2 | GRCh38.p7 | 10:35123456 | TTAGGATGAACTATA[A/C]TGGAAGTACCAGATG | 8453 |
rs1926554 | snp | A/G | 0.41833 | 0.184838 | intron-variant | CUL2 | GRCh38.p7 | 10:35056041 | GTAAAACAGTTGTGC[A/G]TTAAATAGTTACTTG | 8453 |
rs1926555 | snp | C/T | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35055980 | CTGGGGTTCAGGGCA[C/T]ACCTGAAAGGTGTGT | 8453 |
rs1926556 | snp | A/G | 0.41833 | 0.184838 | intron-variant | CUL2 | GRCh38.p7 | 10:35055979 | TGGGGTTCAGGGCAC[A/G]CCTGAAAGGTGTGTC | 8453 |
rs2001893 | snp | C/T | 0.463234 | 0.130503 | intron-variant | CUL2 | GRCh38.p7 | 10:35011695 | AGAATCGTACTCACT[C/T]ACAATTTCAGTATTA | 8453 |
rs2126984 | snp | A/G | 0.46865 | 0.121211 | intron-variant | CUL2 | GRCh38.p7 | 10:35121363 | CTCCCAAGTAGCAGC[A/G]ACTATAGGCACACCA | 8453 |
rs2148482 | snp | C/T | 0.439918 | 0.162576 | intron-variant | CUL2 | GRCh38.p7 | 10:35059982 | atgagccactgtgcc[C/T]ggctAAATTAGTACT | 8453 |
rs2148483 | snp | C/T | 0.205417 | 0.245993 | intron-variant | CUL2 | GRCh38.p7 | 10:35052373 | CACATCCTGAAGTTT[C/T]GCAGCTCTGCCCCAT | 8453 |
rs2182516 | snp | A/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35060274 | ttttgtccttttttt[A/T]attttttattttttg | 8453 |
rs2243807 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35104205 | TAATCCCAGCACTTA[C/G]GGATGCCGAGGAAGG | 8453 |
rs2244100 | snp | A/G | 0.483708 | 0.088773 | intron-variant | CUL2 | GRCh38.p7 | 10:35034708 | GAGGGTTATTGTTTT[A/G]GGTATTTGGGGCAGC | 8453 |
rs2244174 | snp | A/G | 0.00252146 | 0.0354176 | intron-variant | CUL2 | GRCh38.p7 | 10:35035148 | GATTAGGAGGAAAAC[A/G]TTGCAGTTTCCCACA | 8453 |
rs2384275 | snp | A/G | 0.462034 | 0.132445 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008214 | TGGGCTGTGTGCTAC[A/G]GCTTCTGCAGTGATG | 8453 |
rs2384276 | snp | A/G | 0.268452 | 0.249318 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008377 | CTCTCTTCCTCATGC[A/G]AGAGATGTTTCCTTT | 8453 |
rs2384280 | snp | C/T | 0.268452 | 0.249318 | intron-variant | CUL2 | GRCh38.p7 | 10:35015934 | CTTCCAGATGGCAAT[C/T]CTTTTACAATTATTC | 8453 |
rs2384281 | snp | C/T | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35036662 | CCTGTTTTTTGAGCA[C/T]TTTATATTTTGGATA | 8453 |
rs2384282 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | CUL2 | GRCh38.p7 | 10:35037145 | ttctagaagtgttat[A/T]tttttaccttgtaca | 8453 |
rs2384283 | snp | A/G | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35037861 | AAACAAAAACAAAAA[A/G]CCTGATTAATGGCCG | 8453 |
rs2384284 | snp | G/T | 0.20511 | 0.245937 | intron-variant | CUL2 | GRCh38.p7 | 10:35038838 | ACTATTACTAAAATA[G/T]GCATTAAATCAAGGG | 8453 |
rs2384285 | snp | A/G | 0.20511 | 0.245937 | intron-variant | CUL2 | GRCh38.p7 | 10:35048288 | GCTTTAATGGAAGCC[A/G]ATTATAACAACAAAA | 8453 |
rs2384286 | snp | C/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35051028 | GACATAAAATAGTGT[C/T]TCCTTGGCCAGGCAC | 8453 |
rs2384287 | snp | A/G | 0.442385 | 0.15965 | intron-variant | CUL2 | GRCh38.p7 | 10:35051631 | aacaacaacaacaac[A/G]aaaaatagtgtctcc | 8453 |
rs2384288 | snp | C/T | 0.22813 | 0.249042 | intron-variant | CUL2 | GRCh38.p7 | 10:35054569 | TAATATCAATGGATA[C/T]TAAGTTAAAGTCAGT | 8453 |
rs2384289 | snp | A/G | 0.468249 | 0.121932 | intron-variant | CUL2 | GRCh38.p7 | 10:35054597 | AGTAGGAAAGCAAAT[A/G]ACTTGCAACTTTAGA | 8453 |
rs2490657 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35012719 | GGAGACAAATATTAA[C/T]TGCCATTTACTTTGA | 8453 |
rs2490658 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35101374 | TACTAATGAGGTCAA[A/T]GTGTGGTCTCCACAT | 8453 |
rs2490660 | snp | G/T | 0.497613 | 0.0344622 | intron-variant | CUL2 | GRCh38.p7 | 10:35089820 | GTTTGTGTGTGTGTG[G/T]GGGGGGGGGCATCTC | 8453 |
rs2490661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35107846 | TGCCCAGGCTGGAGT[A/G]CAGTGGCGCGATCTA | 8453 |
rs2490662 | snp | G/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35060252 | TATTTTTTGAGGCAG[G/T]ATCTCACCTAGGCTG | 8453 |
rs2490663 | snp | C/T | 0.487241 | 0.0788465 | intron-variant | CUL2 | GRCh38.p7 | 10:35040807 | AGGATGTGCGCTCTT[C/T]AGAAGAATCTAATGC | 8453 |
rs2490664 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | CUL2 | GRCh38.p7 | 10:35028634 | GTAGTTACTAATATT[A/G]ATACTAAAATGCTAA | 8453 |
rs2490665 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CUL2 | GRCh38.p7 | 10:35014395 | GATACAGAAGTTGTT[A/G]TTCTAAAAATTGCCT | 8453 |
rs2505631 | snp | A/T | 0.487241 | 0.0788465 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079457 | ctgtgccagaaagca[A/T]tgagcctatttgaag | 8453 |
rs2505632 | snp | A/G | 0.257732 | 0.24988 | intron-variant | CUL2 | GRCh38.p7 | 10:35073590 | AAGAAAAAGAAAAAA[A/G]AAAAGAAAAGAAAAG | 8453 |
rs2505633 | snp | A/G | 0.266546 | 0.249452 | intron-variant | CUL2 | GRCh38.p7 | 10:35071629 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 8453 |
rs2505634 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CUL2 | GRCh38.p7 | 10:35070646 | TGACTGGGGTGGAAG[C/T]GTGTTTTTCATTAGA | 8453 |
rs2505635 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35066727 | AATTGATATTTGTTC[A/T]CATTGATTCACTAGC | 8453 |
rs2505642 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | CUL2 | GRCh38.p7 | 10:35028570 | AGCAGATGATAGACT[A/T]ACTCAGAATAAGAGA | 8453 |
rs2891473 | snp | A/G | 0.270621 | 0.249148 | intron-variant | CUL2 | GRCh38.p7 | 10:35116109 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATAAC | 8453 |
rs3065352 | in-del | -/TA/TATA | 0 | 0 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009221 | ATATATATATATATA[-/TA/TATA]AAATAAACAAAATAA | 8453 |
rs3065383 | in-del | -/CCT/CCTA | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35048220 | ACATGCAAAACTCTA[-/CCT/CCTA]AGAGAGCTGTCATGA | 8453 |
rs3065413 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075683 | cacacacacacacac[-/AC]GCACGCTCCACattt | 8453 |
rs3740083 | snp | A/G | 0.444133 | 0.157519 | intron-variant | CUL2 | GRCh38.p7 | 10:35031455 | TTTCATTTGTATTTT[A/G]GTCAACTTTATTTCT | 8453 |
rs3780888 | snp | A/G | 0.253824 | 0.249971 | intron-variant | CUL2 | GRCh38.p7 | 10:35028389 | GTAAATATATGTGAA[A/G]TAACTGCTAGTAGAG | 8453 |
rs3780889 | snp | A/C/G | 0.52327 | 0.207721 | intron-variant | CUL2 | GRCh38.p7 | 10:35010787 | ATGCACTGAAGGAAA[A/C/G]GTATACAGTACTATG | 8453 |
rs4244993 | snp | A/G | 0.268995 | 0.249277 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008755 | AATGCAATTGAATAA[A/G]CCAATTGTAAGACCC | 8453 |
rs4244994 | snp | A/T | 0.422315 | 0.181128 | intron-variant | CUL2 | GRCh38.p7 | 10:35050133 | CAAGACCATCCTGGC[A/T]AACATGGCAAAACCC | 8453 |
rs4582914 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | CUL2 | GRCh38.p7 | 10:35050310 | TGGTGACAACAGTGC[A/G]AGACTCCGTCTCAAA | 8453 |
rs4598625 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35031482 | GAAACTTTTCTGTTC[A/G]CAACATACCTTTTGA | 8453 |
rs4934529 | snp | A/T | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35013448 | TTCGGAGAGAATGCA[A/T]AGTTACACATTCTAA | 8453 |
rs4934530 | snp | C/T | 0.26818 | 0.249338 | intron-variant | CUL2 | GRCh38.p7 | 10:35021769 | TGTGGGCTGTGATCG[C/T]GCACCTCCACTCCAG | 8453 |
rs4934531 | snp | C/T | 0.253824 | 0.249971 | intron-variant | CUL2 | GRCh38.p7 | 10:35021929 | AGTGGGGCGAGGGGG[C/T]ACCCGGCCCTATTAG | 8453 |
rs4934533 | snp | A/G | 0.464416 | 0.128553 | intron-variant | CUL2 | GRCh38.p7 | 10:35070691 | CACTCTCCAGCAAGC[A/G]CACTCTTCCCCCCAA | 8453 |
rs4934699 | snp | A/G | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35017648 | CAGTGAGCCAAGATC[A/G]CACCACTGCACTCAA | 8453 |
rs4934700 | snp | A/G | 0.406296 | 0.19512 | intron-variant | CUL2 | GRCh38.p7 | 10:35021914 | GGTGAGGTGGGGCGA[A/G]GTGGGGCGAGGGGGC | 8453 |
rs4934701 | snp | C/T | 0.26818 | 0.249338 | intron-variant | CUL2 | GRCh38.p7 | 10:35021974 | TTGAGATGTGATTTC[C/T]CCAGAAGACTTCCCT | 8453 |
rs4934702 | snp | C/T | 0.442113 | 0.159977 | intron-variant | CUL2 | GRCh38.p7 | 10:35034146 | ACTTAACTAAGTCAG[C/T]TGGATTTGAGTCTAC | 8453 |
rs4934704 | snp | C/T | 0.444533 | 0.157025 | intron-variant | CUL2 | GRCh38.p7 | 10:35043236 | TTTTTGACAGCCAGA[C/T]AGAGCAAAGTGCATG | 8453 |
rs4934705 | snp | C/T | 0.418169 | 0.184985 | intron-variant | CUL2 | GRCh38.p7 | 10:35045606 | TGTGGTCCCAGCTAC[C/T]CTGGAGGCTGAGGTG | 8453 |
rs4934706 | snp | C/T | 0.444931 | 0.15653 | intron-variant | CUL2 | GRCh38.p7 | 10:35045667 | GGCTACAGTGAGCCA[C/T]GATTGCACCACTGCA | 8453 |
rs4934707 | snp | C/G | 0.418007 | 0.185132 | intron-variant | CUL2 | GRCh38.p7 | 10:35045685 | TTGCACCACTGCACT[C/G]CAGCCTGGGTGACAG | 8453 |
rs4934708 | snp | A/C | 0.254944 | 0.249951 | intron-variant | CUL2 | GRCh38.p7 | 10:35047235 | GAAACCCTACCTCAA[A/C]CTCCATATTTGCTTA | 8453 |
rs4934709 | snp | A/C | 0.441841 | 0.160303 | intron-variant | CUL2 | GRCh38.p7 | 10:35050396 | CTATAGATACCTAGA[A/C]CGTAACAGAAACAAA | 8453 |
rs4934710 | snp | C/T | 0.41833 | 0.184838 | intron-variant | CUL2 | GRCh38.p7 | 10:35061488 | AAAAAATCACACTTA[C/T]AATGTAACCTAAAAT | 8453 |
rs4934711 | snp | A/G | 0.452088 | 0.147217 | intron-variant | CUL2 | GRCh38.p7 | 10:35071382 | TAGCAATAATTCCAT[A/G]AGCTTAGTTTTTTTG | 8453 |
rs4934712 | snp | A/G | 0.27008 | 0.249192 | intron-variant | CUL2 | GRCh38.p7 | 10:35071554 | GGACTACAGGCACCC[A/G]CCACCATGCCCAGCT | 8453 |
rs4934714 | snp | C/G | 0.0551013 | 0.156571 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075887 | GAATTATAAAACGCA[C/G]CTACCATATGACCCA | 8453 |
rs4934715 | snp | G/T | 0.435119 | 0.16802 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076064 | ttaaaatgcaatata[G/T]ccatacaataaatta | 8453 |
rs4934716 | snp | A/G | 0.446249 | 0.154875 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080371 | TAAGGTTTGACCCAC[A/G]GAGCTCTAAGTACTC | 8453 |
rs4934717 | snp | C/T | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35082328 | ATGGTCCTATTTAAA[C/T]AAAAGTATGTATGTG | 8453 |
rs4934718 | snp | A/T | 0.433818 | 0.169443 | intron-variant | CUL2 | GRCh38.p7 | 10:35085422 | gcgacaaagcgagac[A/T]ccgtcccaaaaaaaa | 8453 |
rs4934719 | snp | C/T | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35087841 | TCTCAATCAGACCTC[C/T]CAGTTTAGAAGAGTT | 8453 |
rs4934720 | snp | C/T | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35087872 | CCAAAAGCCTTTTAA[C/T]GTATCTAAGAACAAA | 8453 |
rs4934721 | snp | A/G | 0.406123 | 0.195258 | intron-variant | CUL2 | GRCh38.p7 | 10:35088787 | TCCAAATACTCAAAA[A/G]GCAATTGAAAAGGAA | 8453 |
rs4934723 | snp | A/G | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35092835 | GGAAGACTAATGAAA[A/G]GCAGCAAGAATAGGA | 8453 |
rs4934724 | snp | C/T | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35104741 | GAATCAAAGACTTTT[C/T]TGGGGGGGGGACAGT | 8453 |
rs4934725 | snp | C/T | 0.40733 | 0.194287 | intron-variant | CUL2 | GRCh38.p7 | 10:35109308 | GGCAGAATTATACAT[C/T]TATGCATCCATCAAT | 8453 |
rs4934726 | snp | A/G | 0.256619 | 0.249912 | intron-variant | CUL2 | GRCh38.p7 | 10:35112416 | GCTTACTGTCTGGAG[A/G]GAGTTTTCAGGCTCC | 8453 |
rs4934729 | snp | C/T | 0.270621 | 0.249148 | intron-variant | CUL2 | GRCh38.p7 | 10:35118303 | GCAATAATTCTTTCA[C/T]ATGTTCTTTTTTTCC | 8453 |
rs4934730 | snp | A/G | 0.407502 | 0.194147 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126627 | CCCTGAAGACCTGAC[A/G]ACAGCCGTTACTCTG | 8453 |
rs5784437 | in-del | -/TTTTTTT | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35011212 | TTTTTAATTTTTTAA[-/TTTTTTT]TTTTTTTTTTTTTTA | 8453 |
rs5784438 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35012054 | AGTGAGTGCAAATAC[-/T]TTTTTTTTTTTTTTT | 8453 |
rs5784440 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35117543 | TTTTTTTTTTTTTTT[-/T]AACTGCTGTAAAAGG | 8453 |
rs6481935 | snp | C/T | 0.463666 | 0.129795 | intron-variant | CUL2 | GRCh38.p7 | 10:35054031 | CCCATTTAATTGTTT[C/T]ACTCTGAATTTAATT | 8453 |
rs7069513 | snp | A/T | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35024518 | CAAAAAAAGAGAAAA[A/T]TCAAGTGTCTGCTTT | 8453 |
rs7074266 | snp | A/G | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35027494 | CCTAGGTAAAAAAGA[A/G]ATGTAACAATTAAGA | 8453 |
rs7074917 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021911 | tggggtgaggtgggg[C/T]gaagtggggcgaggG | 8453 |
rs7079205 | snp | C/T | 0.434398 | 0.168811 | intron-variant | CUL2 | GRCh38.p7 | 10:35035691 | ataatttcttaacaa[C/T]tgatggaaatttagg | 8453 |
rs7079249 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35046990 | TTTGCTTTTCCTATA[C/T]GAACTCTACCATTGG | 8453 |
rs7079498 | snp | C/T | 0.429238 | 0.174281 | intron-variant | CUL2 | GRCh38.p7 | 10:35086416 | cctcaacctccctag[C/T]agctgggattacagg | 8453 |
rs7084196 | snp | C/T | 0.4444 | 0.15719 | intron-variant | CUL2 | GRCh38.p7 | 10:35078233 | CAAAATGTCCACCCC[C/T]AAAAAACTTAAATTA | 8453 |
rs7095213 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35046848 | cagtgagccaagatc[A/G]tgccacggcattcta | 8453 |
rs7097545 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CUL2 | GRCh38.p7 | 10:35116595 | AATTTTCCTTATTTA[C/T]GATGTAAGAATATGA | 8453 |
rs7098557 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | CUL2 | GRCh38.p7 | 10:35060141 | cggtgcacacctgtt[C/G]ttccagcaactgggg | 8453 |
rs7099036 | snp | C/T | 0.4444 | 0.15719 | intron-variant | CUL2 | GRCh38.p7 | 10:35060646 | ACAGAGCCATGCAAT[C/T]GAGTACAGTTTTACT | 8453 |
rs7099593 | snp | A/C | 0.44638 | 0.154709 | intron-variant | CUL2 | GRCh38.p7 | 10:35077950 | GTTAAGGATGAATAA[A/C]AGGGACATGGGGATT | 8453 |
rs7100929 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | CUL2 | GRCh38.p7 | 10:35102815 | ttgaacctggggggc[A/G]gaagttgcaatgagc | 8453 |
rs7393949 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021901 | tggggtgaggtgggg[C/T]gaggtggggcgaagt | 8453 |
rs7475902 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123197 | GGACTTCATGCCAAA[C/T]TTAGTTACACTCTGT | 8453 |
rs7896522 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CUL2 | GRCh38.p7 | 10:35049435 | CTCAGATACTTATTT[A/G]TATACTAAGCATATT | 8453 |
rs7897024 | snp | C/T | 0.0192684 | 0.0962441 | synonymous-codon, intron-variant | CUL2 | GRCh38.p7 | 10:35049745 | TTCAACCATCAATTT[C/T]CTCCACATATCCAAT | 8453 |
rs7897457 | snp | A/G | 0.445196 | 0.1562 | intron-variant | CUL2 | GRCh38.p7 | 10:35097112 | accgtgcccagccTC[A/G]TGccccttttcttca | 8453 |
rs7897827 | snp | C/T | 0.434253 | 0.168969 | intron-variant | CUL2 | GRCh38.p7 | 10:35097309 | ttggatttttcctag[C/T]tgtacccttaagctg | 8453 |
rs7899633 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | CUL2 | GRCh38.p7 | 10:35046181 | GAGAATCTTGATATC[G/T]TGATATCACTGACTA | 8453 |
rs7900480 | snp | A/G | 0.460915 | 0.13422 | intron-variant | CUL2 | GRCh38.p7 | 10:35049771 | CCAATGCTAGCTGCC[A/G]GGAAAAACGAAAATC | 8453 |
rs7902166 | snp | A/C | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128274 | AGAAATTGGGACTTA[A/C]AGGGCCAGTCTCAAA | 8453 |
rs7903738 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35019312 | AGCATTAGGAGATCA[C/T]GCGAGGGGCCAAAGC | 8453 |
rs7904087 | snp | A/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35116635 | GATTTAAAAAACATT[A/T]TGTCAAGTATTTAGT | 8453 |
rs7907294 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | CUL2 | GRCh38.p7 | 10:35060459 | AAATAACCCAGTAAT[G/T]TATCTAACATCGTTT | 8453 |
rs7908573 | snp | C/T | 0.417845 | 0.185278 | intron-variant | CUL2 | GRCh38.p7 | 10:35020585 | CCATACTATGTACTG[C/T]CTGGTGAAGTTTTTT | 8453 |
rs7912881 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35088376 | agctgggcgtggtga[C/T]gtgcgcctgtagtgc | 8453 |
rs7914693 | snp | C/G | 0.0603597 | 0.1629 | intron-variant | CUL2 | GRCh38.p7 | 10:35053540 | CTGTTCAGCCATTAG[C/G]CACCCTATTAACAAT | 8453 |
rs7918498 | snp | A/G | 0.159622 | 0.233092 | intron-variant | CUL2 | GRCh38.p7 | 10:35114212 | caagtgtgagccacc[A/G]cacctggccccgtat | 8453 |
rs7919782 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | CUL2 | GRCh38.p7 | 10:35101967 | ATAAAATAAGAAAca[A/G]cctcccaaaatgctg | 8453 |
rs7920095 | snp | A/G | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35014406 | AGAATAACAACTTCT[A/G]TATCAGGCTTAAGAA | 8453 |
rs7923172 | snp | A/G | 0.444 | 0.157683 | intron-variant | CUL2 | GRCh38.p7 | 10:35020439 | TTGAAAACAAAAGCA[A/G]GACAAATTTAGTCAA | 8453 |
rs7923217 | snp | A/G | 0.46754 | 0.123192 | intron-variant | CUL2 | GRCh38.p7 | 10:35020661 | TGACCAGCAATCTCT[A/G]CAACTTCTTGCTCTG | 8453 |
rs9299717 | in-del | -/T | 0.487241 | 0.0788465 | intron-variant | CUL2 | GRCh38.p7 | 10:35066475 | GCTAATTTTTTTGTA[-/T]TTTTAGTAAAGATGG | 8453 |
rs9299718 | in-del | -/A | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35088521 | AAAAAAAAAAAAAAA[-/A]GAAATGTAATGTGTC | 8453 |
rs9299719 | in-del | -/TGCTCAT | 0.0707826 | 0.174302 | intron-variant | CUL2 | GRCh38.p7 | 10:35118683 | ATGATTTTCCCTCTG[-/TGCTCAT]TGCTCATACTTATTC | 8453 |
rs9336970 | in-del | -/A | 0.0715223 | 0.175059 | intron-variant | CUL2 | GRCh38.p7 | 10:35087884 | AATGTATCTAAGAAC[-/A]AAAGCCAACATGATC | 8453 |
rs9794325 | snp | A/G | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35039919 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC | 8453 |
rs10047349 | snp | A/G | 0.435694 | 0.167385 | intron-variant | CUL2 | GRCh38.p7 | 10:35115127 | tgaggcaggagaatc[A/G]cttgaacccaggagg | 8453 |
rs10160202 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CUL2 | GRCh38.p7 | 10:35032824 | AGTTCATGTAAAACA[C/T]ATCTATTCTCTTTTC | 8453 |
rs10437420 | snp | A/C | 0.467642 | 0.123012 | intron-variant | CUL2 | GRCh38.p7 | 10:35046116 | TGGATATTCTGAGAA[A/C]TATTTTTTGGACATG | 8453 |
rs10466072 | snp | C/T | 0.468249 | 0.121932 | intron-variant | CUL2 | GRCh38.p7 | 10:35113828 | tctcctgcatcaggc[C/T]cctgagaagctggga | 8453 |
rs10508815 | snp | A/C | 0.463343 | 0.130326 | intron-variant | CUL2 | GRCh38.p7 | 10:35043693 | GTTTAATTTGTATGA[A/C]CACTTTTTTCTTCTA | 8453 |
rs10539398 | in-del | -/GAA | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35049518 | GAAGAAGAAGAAGAA[-/GAA]AATAAAACAACTTAA | 8453 |
rs10540491 | in-del | -/AAG | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35049510 | AAAGAAAAAAAAAGA[-/AAG]AAGAAGAAGAAGAAG | 8453 |
rs10589195 | in-del | -/TTAT | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35119606 | tatttatttatttat[-/TTAT]Agagacagggtctca | 8453 |
rs10624287 | in-del | -/CTAC | 0.463343 | 0.130326 | intron-variant | CUL2 | GRCh38.p7 | 10:35048217 | TTAACATGCAAAACT[-/CTAC]CTAAGAGAGCTGTCA | 8453 |
rs10671397 | in-del | -/CT | 0.464416 | 0.128553 | intron-variant | CUL2 | GRCh38.p7 | 10:35054269 | ACATCTTTTTCGTTC[-/CT]CTGAGGATTCTTAGG | 8453 |
rs10678495 | in-del | -/TTTA | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080470 | TATTTATTTATTTAT[-/TTTA]TTATTTATTTTTGAG | 8453 |
rs10714791 | in-del | -/A | 0.405429 | 0.195811 | intron-variant | CUL2 | GRCh38.p7 | 10:35022079 | TGTAACTATGTACGT[-/A]TGTCTGTCTTCCTAC | 8453 |
rs10714792 | in-del | -/G | 0.405429 | 0.195811 | intron-variant | CUL2 | GRCh38.p7 | 10:35022077 | ACTGTAACTATGTAC[-/G]TATGTCTGTCTTCCT | 8453 |
rs10827487 | snp | A/T | 0.43555 | 0.167544 | intron-variant | CUL2 | GRCh38.p7 | 10:35117950 | aagtacacagttcct[A/T]tcatcccctccccca | 8453 |
rs11010068 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35012667 | AAATTATTATTTATT[A/G]GCCTGGAGGAAAATG | 8453 |
rs11010069 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017890 | Taaaaaaaaaaaaaa[A/G]gaaaagaaaaaaGAT | 8453 |
rs11010070 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017895 | aaaaaaaaaaagaaa[A/G]gaaaaaaGATGCAGA | 8453 |
rs11010071 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35017953 | GTTGTGGTTTGACGA[C/T]TAACACACACACGGC | 8453 |
rs11010072 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018121 | tgctctactaaaaat[A/C]caaaaaaaaaaaaaa | 8453 |
rs11010073 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | CUL2 | GRCh38.p7 | 10:35022441 | TAGACTAGGCAAGAA[A/T]AATTTTCATTCTATG | 8453 |
rs11010074 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35028337 | ATTAGTTATTACCAC[A/G]AAACTAATAACCACT | 8453 |
rs11010077 | snp | A/G | 0.465052 | 0.127485 | intron-variant | CUL2 | GRCh38.p7 | 10:35039160 | ATCAGCAAGTAACTC[A/G]GCCAAATTTTAATGG | 8453 |
rs11010078 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35042438 | TAGTTACAGTCTTTA[A/G]TTATAATGTTGAGTG | 8453 |
rs11010079 | snp | C/G | 0.0607341 | 0.163335 | intron-variant | CUL2 | GRCh38.p7 | 10:35051897 | TAAAAATATATTAAA[C/G]TTTAATATACTCAAA | 8453 |
rs11010080 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35052425 | CTGACACCCAGTCTA[G/T]AAAAAGTTCTGCTCA | 8453 |
rs11010081 | snp | C/G | 0.0681886 | 0.171594 | intron-variant | CUL2 | GRCh38.p7 | 10:35057820 | AGACATGGGCTGGAC[C/G]CAGTGGCTCACGCCT | 8453 |
rs11010082 | snp | A/G | 0.467946 | 0.122472 | intron-variant | CUL2 | GRCh38.p7 | 10:35062227 | TGCCCCTCTATGTAC[A/G]GCATACTAATAAAAA | 8453 |
rs11010083 | snp | C/G | 0.445987 | 0.155207 | intron-variant | CUL2 | GRCh38.p7 | 10:35062603 | AAGGGAGGCCAAGGC[C/G]GGAGGATCACTGGAG | 8453 |
rs11010084 | snp | A/G | 0.48435 | 0.0870631 | intron-variant | CUL2 | GRCh38.p7 | 10:35071692 | GGATTACAGGCATGA[A/G]CCATCACACCCGGCC | 8453 |
rs11010085 | snp | G/T | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35076192 | agccacataacgtat[G/T]aatctatttatatag | 8453 |
rs11010087 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099159 | gcactttgggaggcc[A/G]aggagggcagatcac | 8453 |
rs11010088 | snp | C/G | 0.434253 | 0.168969 | intron-variant | CUL2 | GRCh38.p7 | 10:35103194 | GTTGCCCAGGCTGCA[C/G]TGCAGTGGTGTGATC | 8453 |
rs11010089 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103333 | ttttttttttttttt[A/T]tttttttttgagacg | 8453 |
rs11010090 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103334 | tttttttttttttta[A/T]ttttttttgagacgg | 8453 |
rs11010091 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103524 | gagacggggtttcac[C/G]gtgtcagccaggatg | 8453 |
rs11010092 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103548 | caggatggtctcgat[C/T]tcctgacctcgtgat | 8453 |
rs11010093 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103571 | ctcgtgatccgcccg[C/T]ctcggcctcccaaag | 8453 |
rs11010095 | snp | A/G | 0.469839 | 0.119042 | intron-variant | CUL2 | GRCh38.p7 | 10:35107020 | CACTCTGTCACCCAG[A/G]GTAGAGTGCAGTGGC | 8453 |
rs11010098 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110615 | TCACAGTTCTGGAGG[C/T]TGGGAGTCCAAGATC | 8453 |
rs11010099 | snp | A/G | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35113584 | ACATCTGGCATCTAC[A/G]AAAAATTACCAAGAA | 8453 |
rs11010100 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114130 | GGTTTCACTGTGTTA[A/G]CCAGGATGGTCTCGA | 8453 |
rs11010101 | snp | A/T | 0.435694 | 0.167385 | intron-variant | CUL2 | GRCh38.p7 | 10:35122117 | AGCACATATTATACT[A/T]ACTTGTTTTTACCTT | 8453 |
rs11010102 | snp | A/T | 0.435694 | 0.167385 | intron-variant | CUL2 | GRCh38.p7 | 10:35122138 | TTTTTACCTTTCTCA[A/T]ATATTTAAATTGGGC | 8453 |
rs11283661 | in-del | -/GATCGC | 0.434253 | 0.168969 | intron-variant | CUL2 | GRCh38.p7 | 10:35030822 | GCTTGAGCCCAGGAG[-/GATCGC]TTAGAGTCCAGCCTG | 8453 |
rs11307339 | in-del | -/A | 0.483636 | 0.0889627 | intron-variant | CUL2 | GRCh38.p7 | 10:35017693 | ATGAGTATCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs11318064 | snp | A/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35030825 | TTGAGCCCAGGAGTT[A/T]GAGTCCAGCCTGGGC | 8453 |
rs11333504 | in-del | -/T | 0.206336 | 0.246157 | intron-variant | CUL2 | GRCh38.p7 | 10:35118263 | TTTCATTCTAAAGTA[-/T]GTCTTCAATTCTGGG | 8453 |
rs11334081 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033789 | AAGAAAGAAAATAGC[-/T]TGTCATTCAACACAA | 8453 |
rs11357517 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018289 | AAGACTCCATCTCAC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs11395891 | in-del | -/A/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018122 | CTCTACTAAAAATAC[-/A/AA]AAAAAAAAAAAAAAA | 8453 |
rs11446830 | in-del | -/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35059459 | AAATGATCAACAGCA[-/T]TTTTTTTTAGCAATA | 8453 |
rs11454447 | in-del | -/A | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35018123 | AAAAAAAAAAAAAAA[-/A]CTAGCAGGGCGCAGT | 8453 |
rs11498306 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075680 | CACACACACACACAC[A/G]CACGCACGCTCCACA | 8453 |
rs11545108 | snp | C/T | 0.0170251 | 0.090679 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35010078 | CACTTTTCAGCAATA[C/T]TTCACTCATTCTTTT | 8453 |
rs11591248 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35012618 | GAGGATCTCCTCACA[C/G]CGTTTCAAAGACAAA | 8453 |
rs11591574 | snp | A/T | 0.213333 | 0.247296 | intron-variant | CUL2 | GRCh38.p7 | 10:35044049 | gagcaagaccacatc[A/T]ccaaaaaaaaaaaaa | 8453 |
rs11591577 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35044145 | TGACTCATCCAAATG[A/T]CTAGAATTACTATAT | 8453 |
rs11591598 | snp | A/G | 0.206642 | 0.246211 | intron-variant | CUL2 | GRCh38.p7 | 10:35053159 | GTTCAGAAAAGATGC[A/G]AACTAAATTGTTTAC | 8453 |
rs11591847 | snp | A/G | 0.269538 | 0.249235 | intron-variant | CUL2 | GRCh38.p7 | 10:35071688 | GCTGGGATTACAGGC[A/G]TGAACCATCACACCC | 8453 |
rs11592064 | snp | C/T | 0.155325 | 0.23138 | intron-variant | CUL2 | GRCh38.p7 | 10:35083806 | CAAGGAGTTCAAAAC[C/T]AGCCTGGAGCATAGC | 8453 |
rs11592567 | snp | C/T | 0.407502 | 0.194147 | utr-variant-5-prime, intron-variant | CUL2 | GRCh38.p7 | 10:35120441 | GCTGGGTTTTCTAGT[C/T]TCTGTTATAAAAAGG | 8453 |
rs11592989 | snp | A/C | 0.108048 | 0.20579 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126101 | tgctgggattacagg[A/C]gtgagcccccgGCCG | 8453 |
rs11593156 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051808 | gttttttatatattg[A/T]ggaAATTAATCCCTT | 8453 |
rs11593858 | snp | A/G | 0.406468 | 0.194981 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35092445 | tatcctggatgaagc[A/G]gaagcattaatttta | 8453 |
rs11594549 | snp | A/C | 0.205417 | 0.245993 | intron-variant | CUL2 | GRCh38.p7 | 10:35015980 | TATAGGACAAATAAA[A/C]TCAAACTATAAACGG | 8453 |
rs11595640 | snp | C/T | 0.211819 | 0.247067 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125596 | AATAATAAATCCTCA[C/T]TTAACATTGTCAATA | 8453 |
rs11595898 | snp | C/T | 0.418007 | 0.185132 | intron-variant | CUL2 | GRCh38.p7 | 10:35037335 | catcaagtggccaca[C/T]atgcttgggttgttt | 8453 |
rs11596128 | snp | A/G | 0.206029 | 0.246103 | intron-variant | CUL2 | GRCh38.p7 | 10:35071644 | TGATCTCCTGACCTC[A/G]TGATCCGCCCACCTT | 8453 |
rs11596502 | snp | G/T | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35098259 | AAAAAGAACTCATTT[G/T]GAGGAAAAGCCCACT | 8453 |
rs11597184 | snp | A/G | 0.410568 | 0.191619 | intron-variant | CUL2 | GRCh38.p7 | 10:35108468 | tcaaaaaaaaaaaaa[A/G]gaaaaaaagaaaaaa | 8453 |
rs11597553 | snp | A/T | 0.119281 | 0.213102 | intron-variant | CUL2 | GRCh38.p7 | 10:35024656 | ATTGTGATAAAAGTT[A/T]TTTAAAATTGGAAAC | 8453 |
rs11597757 | snp | A/T | 0.155325 | 0.23138 | intron-variant | CUL2 | GRCh38.p7 | 10:35040164 | GTCTCAAAAAATAAA[A/T]ATAAATAAAAAATAA | 8453 |
rs11597912 | snp | A/G | 0.204803 | 0.245881 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009055 | ACATGGCGAAACCCC[A/G]TCTCTTATTTTTTTT | 8453 |
rs11597913 | snp | C/T | 0.206336 | 0.246157 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125300 | ATGAACAAAAAAATA[C/T]GGTTTGTGCTTTCTG | 8453 |
rs11598363 | snp | C/T | 0.147991 | 0.228242 | intron-variant | CUL2 | GRCh38.p7 | 10:35046744 | TAAAAATACAAAAAT[C/T]AGCTGGGCATGGTGG | 8453 |
rs11599183 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35051520 | cgggaggctgaggca[A/G]gagaatggcgtgaac | 8453 |
rs11599196 | snp | A/C | 0.208169 | 0.246476 | intron-variant | CUL2 | GRCh38.p7 | 10:35098776 | TCTCTACTAAAAAAA[A/C]CCAAAAAATTAGCTG | 8453 |
rs11599606 | snp | A/G | 0.407674 | 0.194008 | intron-variant | CUL2 | GRCh38.p7 | 10:35117698 | CTACATGTGAGTGGT[A/G]TATTACTGAAGGTTC | 8453 |
rs11599898 | snp | A/C | 0.20511 | 0.245937 | intron-variant | CUL2 | GRCh38.p7 | 10:35040182 | AAATAAAAAATAAAA[A/C]ATTTGAAAGTAAATA | 8453 |
rs11819221 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35039577 | ATTAAAATTTTTGAA[A/T]GTAGGggctggacat | 8453 |
rs12184386 | snp | C/T | 0.434398 | 0.168811 | intron-variant | CUL2 | GRCh38.p7 | 10:35034202 | ATCTCCCAGCCTTGA[C/T]ACAAAATTCGATGCT | 8453 |
rs12220175 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103713 | gatctgcccacctca[A/G]cctcctaaagtgctg | 8453 |
rs12220796 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35105537 | agtggaaacccgtct[C/T]tactaaaaaaataca | 8453 |
rs12240347 | snp | A/G | 0.463666 | 0.129795 | intron-variant | CUL2 | GRCh38.p7 | 10:35070547 | CTGTCATGGAGGAAC[A/G]CAGGAAACTAGGCTT | 8453 |
rs12242284 | snp | A/C | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35013619 | GTGCAAAGTTTTGCA[A/C]AATCTCAATGTAAAC | 8453 |
rs12242882 | snp | C/G | 0.463666 | 0.129795 | intron-variant | CUL2 | GRCh38.p7 | 10:35058932 | aaccctcatggatga[C/G]ttagggggtcaagac | 8453 |
rs12245096 | snp | C/T | 0.463666 | 0.129795 | intron-variant | CUL2 | GRCh38.p7 | 10:35051081 | agcactttgggaggc[C/T]gagacgggcggatca | 8453 |
rs12248333 | snp | A/G | 0.464131 | 0.129027 | intron-variant | CUL2 | GRCh38.p7 | 10:35074049 | GTGTGCAACCATGCT[A/G]CCTCACTAACATGCT | 8453 |
rs12248391 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35044067 | aaaaaaaaaaaaaaa[A/C]aaaaaaaaCACCTCA | 8453 |
rs12250115 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35013628 | TTTGCACAATCTCAA[C/T]GTAAACACTTGTAAA | 8453 |
rs12250573 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35037881 | ATTAATggccgggcg[C/T]ggtgactcacacctg | 8453 |
rs12250616 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35067883 | gaggctgaggcaggc[A/G]gatcacgaggtcagg | 8453 |
rs12250856 | snp | A/C | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35034900 | ACACAGTTATTTAAA[A/C]ATGGCGAGCTTATTT | 8453 |
rs12252639 | snp | G/T | 0.0678174 | 0.1712 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128854 | TTGATTCTTTTTTTG[G/T]ATAAACTTTCCCTTC | 8453 |
rs12252747 | snp | C/G | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35038767 | CACTTTCCTAAAATA[C/G]TCTTTCAAAATAAAG | 8453 |
rs12253222 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123841 | tgaatgaagttggaa[A/G]ctttgggtataaatt | 8453 |
rs12256738 | snp | C/T | 0.0681886 | 0.171594 | missense | CUL2 | GRCh38.p7 | 10:35100950 | GTTTTCTTTCCATGT[C/T]GCCATGGGTTTTCGT | 8453 |
rs12261333 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CUL2 | GRCh38.p7 | 10:35043541 | AGGGATGTAGGATGA[C/T]AGCTCACCCACTTAA | 8453 |
rs12261654 | snp | A/G | 0.445987 | 0.155207 | intron-variant | CUL2 | GRCh38.p7 | 10:35033096 | TCATACTAGAATTCT[A/G]ATCTTGAAACTGCCT | 8453 |
rs12263295 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009314 | GTTATGCATTGCTAA[A/C/G]CACATCTGTGATTGA | 8453 |
rs12263376 | snp | A/G | 0 | 0 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009436 | ATTTCCTAAGACTCA[A/G]GGAAGGCCACAGAGC | 8453 |
rs12263386 | snp | C/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009566 | CATCCTGCTCACACT[C/T]TGCGATGTCTGTGGA | 8453 |
rs12263550 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35037591 | tggctcgtgtctata[A/G]tcccagcactttggg | 8453 |
rs12263773 | snp | A/T | 0.463343 | 0.130326 | intron-variant | CUL2 | GRCh38.p7 | 10:35027210 | AGTGCAGTGGCGCAA[A/T]CTCGGCTCACTGCAA | 8453 |
rs12264975 | snp | C/G | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35050658 | aacatacagccatag[C/G]tcaatcattggcact | 8453 |
rs12266808 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35051175 | aaaaaattagcgggg[C/T]gtggtggcgggtgcc | 8453 |
rs12268587 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35057650 | ggagcaagactccgt[C/T]tgaaaaaaaaaaaaa | 8453 |
rs12268745 | snp | C/G | 0.444799 | 0.156695 | intron-variant | CUL2 | GRCh38.p7 | 10:35017061 | TGGACAGACAAAGGG[C/G]AAAGTGATATCAGCA | 8453 |
rs12268916 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35103323 | atttttttttttttt[A/T]tttttttttattttt | 8453 |
rs12269154 | snp | G/T | 0.0633504 | 0.166319 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008599 | ATCAAAACAAGGGTT[G/T]GCTTTTTGACAGTGA | 8453 |
rs12357844 | snp | A/G | 0.431473 | 0.171952 | intron-variant | CUL2 | GRCh38.p7 | 10:35046252 | GCTTGGGTCACATGC[A/G]TGACCTCACATAAGC | 8453 |
rs12411998 | snp | A/C | 0.00938946 | 0.0678717 | intron-variant | CUL2 | GRCh38.p7 | 10:35101868 | TTTCTAATTAGAGGG[A/C]GTAGAACTAACAGAG | 8453 |
rs12412935 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35017873 | AATGTTCCATACGTG[G/T]TTaaaaaaaaaaaaa | 8453 |
rs12413312 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35092874 | ggggtgtgaactttg[C/T]taaagtgtaggcata | 8453 |
rs12415636 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | CUL2 | GRCh38.p7 | 10:35037682 | acctcgtctctacta[A/C]aaatacaaaaattag | 8453 |
rs12570287 | snp | A/T | 0.444444 | 0.157135 | intron-variant | CUL2 | GRCh38.p7 | 10:35043114 | ttgagagagtttttc[A/T]CTACACACGAtgaat | 8453 |
rs12573435 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CUL2 | GRCh38.p7 | 10:35102389 | ccagcctggccaaca[C/T]agtgaaatcctgtct | 8453 |
rs12761884 | snp | A/C | 0.0912534 | 0.193131 | intron-variant | CUL2 | GRCh38.p7 | 10:35021568 | atgtattaaataaaa[A/C]cccatttcatttaca | 8453 |
rs12763028 | snp | C/T | 0.205417 | 0.245993 | intron-variant | CUL2 | GRCh38.p7 | 10:35030505 | CTCCCACCTCAGCCA[C/T]CTGAGTAACTGGGAC | 8453 |
rs12764135 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127331 | ccgtgggcggcgggc[C/T]gggaccccggggccg | 8453 |
rs12764438 | snp | C/G | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127313 | agcagaggccgagcg[C/G]agccgtgggcggcgg | 8453 |
rs12764516 | snp | A/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127559 | CGGAAAAGGAAAAGG[A/T]ATCCAGAAGTAAGGA | 8453 |
rs12764820 | snp | A/G | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35097393 | gcctggggaggctga[A/G]gtggaaggattgctt | 8453 |
rs12764854 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127533 | GTGCGGCTCAGGGGA[C/G]CGGTTTAACTCGGAA | 8453 |
rs12764861 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127546 | GAGCGGTTTAACTCG[C/G]AAAAGGAAAAGGAAT | 8453 |
rs12765038 | snp | C/G | 0.43598 | 0.167067 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127585 | AAGGACCTCGGATTT[C/G]AGTGCCCCCAGCGCC | 8453 |
rs12765063 | snp | A/G | 0.207559 | 0.246371 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127641 | TAGACGAAAGCGGAC[A/G]CAGCCCGTTTTCCCC | 8453 |
rs12766191 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113226 | agcggccaggtgcgg[G/T]ggctcacttctgtaa | 8453 |
rs12767102 | snp | C/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35101125 | GTGGGAATACAGGAA[C/T]CTTATTCAGATCAGA | 8453 |
rs12767414 | snp | C/T | 0.467337 | 0.123551 | intron-variant | CUL2 | GRCh38.p7 | 10:35101265 | GACATTCACCTGATG[C/T]CGCTGGCAATAGTGG | 8453 |
rs12767868 | snp | A/C | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35101607 | GAACTGAAGAGTTAC[A/C]AGTGGGATGCTAGGT | 8453 |
rs12768019 | snp | C/T | 0.406123 | 0.195258 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35100915 | AAGCTGTCCTGTGCT[C/T]TTCCTCTCTATATCA | 8453 |
rs12769109 | snp | A/G | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35022561 | CCTTAGGCCATATAT[A/G]GGTAATCTAGAACAA | 8453 |
rs12769189 | snp | A/G | 0.407674 | 0.194008 | intron-variant | CUL2 | GRCh38.p7 | 10:35110740 | gctgcctcttcacac[A/G]tttgtctctgtgtgc | 8453 |
rs12769981 | snp | A/G | 0.441705 | 0.160466 | intron-variant | CUL2 | GRCh38.p7 | 10:35067846 | gacgtggtggctcat[A/G]cctgtaatcccagca | 8453 |
rs12771315 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075676 | cacacacacacacac[A/G]cacacacgcacGCTC | 8453 |
rs12773146 | snp | A/C | 0.208474 | 0.246527 | intron-variant | CUL2 | GRCh38.p7 | 10:35086164 | agattgagcccctgc[A/C]ctccagactgagaga | 8453 |
rs12773169 | snp | C/G | 0.444533 | 0.157025 | intron-variant | CUL2 | GRCh38.p7 | 10:35077534 | aaaagaaaTAAAAAT[C/G]Aggccagatgtggtg | 8453 |
rs12774536 | snp | A/G | 0.208779 | 0.246578 | intron-variant | CUL2 | GRCh38.p7 | 10:35056507 | TGCCAAAGGTCAATC[A/G]GCTCCTAAGTGGCAG | 8453 |
rs12774834 | snp | A/T | 0.40733 | 0.194287 | intron-variant | CUL2 | GRCh38.p7 | 10:35111142 | tcagtttttggcctg[A/T]gcaacttggttgcca | 8453 |
rs12775079 | snp | A/G | 0.206029 | 0.246103 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080860 | GGAAAACATCTTGAA[A/G]TCTCAAAAAGGGTGA | 8453 |
rs12775759 | snp | G/T | 0.40733 | 0.194287 | intron-variant | CUL2 | GRCh38.p7 | 10:35111255 | CTTCTCTTATGAGAA[G/T]Atttttttttttttt | 8453 |
rs12776390 | snp | G/T | 0.434976 | 0.168179 | intron-variant | CUL2 | GRCh38.p7 | 10:35102607 | ATAAATTTAAAGGCC[G/T]GGCACCGTGGCTCAT | 8453 |
rs12777222 | snp | A/G | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35099024 | ATGTGGTAAGTCTGG[A/G]GGGAAGCTAATTCAC | 8453 |
rs12777476 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114823 | aaaatgcaaggtctg[A/C]aataaaaaatacatt | 8453 |
rs12777654 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114871 | cagatgctgcagaag[A/C]aaacatcaatgaatt | 8453 |
rs12777656 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35114873 | gatgctgcagaagaa[A/T]acatcaatgaatttg | 8453 |
rs12778142 | snp | G/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35114861 | atttaaagatcagat[G/T]ctgcagaagaaaaca | 8453 |
rs12778629 | snp | C/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35099580 | GACTAGCTTAGTCAA[C/T]GTGGTGAAAGCCCGT | 8453 |
rs12782377 | snp | C/T | 0.206029 | 0.246103 | intron-variant | CUL2 | GRCh38.p7 | 10:35112293 | aaaacaactagaaaa[C/T]cagacagagtacata | 8453 |
rs12785044 | snp | C/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35052735 | CCCGCCTCTACTAAA[C/T]ATACAAAAAATTAGC | 8453 |
rs13376801 | snp | C/T | 0.44638 | 0.154709 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081515 | TGAATTTCTGAGTCC[C/T]TCATGACTAGGCAAG | 8453 |
rs13376871 | snp | A/G | 0.449853 | 0.150196 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080128 | TAAGGGAGGCAGGGA[A/G]GTGGAATACCATATT | 8453 |
rs13377158 | snp | G/T | 0.44638 | 0.154709 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081537 | CTAGGCAAGCCCATC[G/T]TGTATGAATACTAGA | 8453 |
rs16935840 | snp | C/T | 0.272398 | 0.248995 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35032486 | GTAATTTACAACTGA[C/T]GTAAGGGCCTGAATA | 8453 |
rs16935856 | snp | C/G | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35040298 | TAATATCAACAAGAA[C/G]TAGCCCATAAGGAAA | 8453 |
rs16935866 | snp | A/C | 0.268995 | 0.249277 | intron-variant | CUL2 | GRCh38.p7 | 10:35046530 | TTTAAGTCTGAGTTC[A/C]TCCTGGTAAAGTTTA | 8453 |
rs16935872 | snp | C/T | 0.268724 | 0.249298 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054728 | TATCAGCCCACCTTT[C/T]TCTGCAAGCCCTTAC | 8453 |
rs16935874 | snp | A/C | 0.254944 | 0.249951 | intron-variant | CUL2 | GRCh38.p7 | 10:35101174 | TCTATCTGGAAGAGT[A/C]TCATAGCCAGTTGGG | 8453 |
rs16935880 | snp | C/G | 0.40733 | 0.194287 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126540 | GCCACTGCAGCCCAG[C/G]CTGGACAGAGGTGAG | 8453 |
rs16935881 | snp | A/C | 0.271162 | 0.249103 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126625 | GACCCTGAAGACCTG[A/C]CRACAGCCGTTACTC | 8453 |
rs16935886 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35127114 | GGCGCCGCTGCTGAG[C/G]GGCGGTCGGGCTCGC | 8453 |
rs17582954 | snp | C/T | 0.263619 | 0.249629 | intron-variant | CUL2 | GRCh38.p7 | 10:35031427 | TTACTTCCTTTCTAA[C/T]GATTTAGCATTCAGA | 8453 |
rs17583009 | snp | C/T | 0.418007 | 0.185132 | intron-variant | CUL2 | GRCh38.p7 | 10:35031987 | TCAAATCATCACTTA[C/T]TGACCAATAAAGCAA | 8453 |
rs17583044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35032615 | AAACACAGCATTGCC[A/G]GTAGTTTGTTAATAT | 8453 |
rs17583107 | snp | C/T | 0.205417 | 0.245993 | intron-variant | CUL2 | GRCh38.p7 | 10:35034505 | ATACACAGATACTAT[C/T]TTATAGATGAAGGGC | 8453 |
rs28625238 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35104768 | CAGTCTTGCTCTTGT[G/T]GCCCAGGCTGCAGTG | 8453 |
rs28636591 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35079915 | ACAGCTACTAAGTGA[C/T]TAATGGCAGGAGGCA | 8453 |
rs28694357 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090720 | GAAATTAATATTCCA[A/G]GTGATTCCTTGCTGG | 8453 |
rs28729730 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021818 | AGGAGAGGCGAGGTG[A/G]GGTGAGGTGAGGCGA | 8453 |
rs28732969 | snp | A/T | 0.375 | 0.216506 | intron-variant | CUL2 | GRCh38.p7 | 10:35021806 | TGAGGTGGGGTGAGG[A/T]GAGGCGAGGTGGGGT | 8453 |
rs28762086 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093670 | CTCTCAAAAAAAAAA[A/G]AAAAAAAAAAAGAAA | 8453 |
rs34018688 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35029807 | AAAGCAACTAATCAA[-/C]AACCTTTCAAACTTT | 8453 |
rs34087268 | snp | G/T | 0.406641 | 0.194842 | intron-variant | CUL2 | GRCh38.p7 | 10:35057796 | AACCACATATTTGCT[G/T]CTTAATAAAGACATG | 8453 |
rs34103783 | in-del | -/AAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021530 | ATACATGTTTATATT[-/AAT]GTCAATTTTAATGTA | 8453 |
rs34149084 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35049337 | CTCACGAGGATTTAA[-/C]ACAGGTAATATGTAC | 8453 |
rs34169199 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35038687 | GAAATTAGCTCTTGT[-/G]AATATATAAAAATGT | 8453 |
rs34178007 | in-del | -/A | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35077338 | AACAAACAAAAAAAA[-/A]CAAACAAAAATTAGC | 8453 |
rs34188875 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35111774 | TGTGCCTGCAATCCC[-/C]AGCTACCAGGGAGGC | 8453 |
rs34213590 | in-del | -/GAAA | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35095346 | AAAAAAAGAAAGAAA[-/GAAA]TACATGCTTTTTGTA | 8453 |
rs34296409 | snp | C/G | 0.407502 | 0.194147 | intron-variant | CUL2 | GRCh38.p7 | 10:35115685 | GATCACTTGAGCCCA[C/G]GAGTTTGAGACCTGC | 8453 |
rs34303523 | in-del | -/T | 0.44333 | 0.158505 | intron-variant | CUL2 | GRCh38.p7 | 10:35017873 | TGTTCCATACGTGTT[-/T]AAAAAAAAAAAAAAA | 8453 |
rs34304999 | snp | C/T | 0.418491 | 0.184691 | intron-variant | CUL2 | GRCh38.p7 | 10:35076777 | ATTTGTGGCCAGGCA[C/T]GGTGGCTCACGCCTG | 8453 |
rs34306263 | snp | C/G | 0.148661 | 0.22854 | intron-variant | CUL2 | GRCh38.p7 | 10:35112038 | GCCTCATTACTCCTT[C/G]TATAAACTCACAACC | 8453 |
rs34319636 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078563 | CCTCAACCTCCCAAA[-/A]GTGCTGGGATTACAG | 8453 |
rs34375045 | snp | A/C | 0.418491 | 0.184691 | intron-variant | CUL2 | GRCh38.p7 | 10:35073428 | ATAGCCCTACAAATG[A/C]TCCGGAATCAGGCCC | 8453 |
rs34386950 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082454 | TCTAGTAACGAAAAA[-/A]GTTTTGGAAATGGTG | 8453 |
rs34427946 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054133 | TAAGTACTTGTCCCC[-/C]TGCACTTTTTAACTA | 8453 |
rs34451255 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127855 | ATACTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 8453 |
rs34481177 | snp | C/T | 0.405776 | 0.195535 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091985 | GGTCTCCCTCTGTCG[C/T]TGAGGCTGGAGTGCA | 8453 |
rs34569047 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039384 | ATAACATGTAACAGG[-/G]AAAAGTGGGTACAGA | 8453 |
rs34575945 | snp | C/T | 0.282105 | 0.24793 | intron-variant | CUL2 | GRCh38.p7 | 10:35029324 | GGCCTCTGAAAGTGC[C/T]GGGATTACAGGCATA | 8453 |
rs34605125 | snp | A/G | 0.408017 | 0.193729 | intron-variant | CUL2 | GRCh38.p7 | 10:35122318 | GATCTGTGGTCTAGT[A/G]GAAAGAGTACAGGGT | 8453 |
rs34646624 | snp | C/T | 0.20511 | 0.245937 | intron-variant | CUL2 | GRCh38.p7 | 10:35040813 | GATTCTTCTAAAGAG[C/T]GCACATCCTAGACCC | 8453 |
rs34658029 | snp | C/T | 0.206029 | 0.246103 | intron-variant | CUL2 | GRCh38.p7 | 10:35068418 | AACTACAACGCACTA[C/T]GTCTAATAAAAAAAA | 8453 |
rs34702637 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077382 | GCTGCCTATAATCCC[-/C]AGCTACTCAAGAGGC | 8453 |
rs34714483 | in-del | -/AC | 0.490725 | 0.0674664 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075636 | CTTATGGGCCCTAAA[-/AC]ACACACACACACACA | 8453 |
rs34721558 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069915 | TTATTAAGATTCTTG[-/G]CCCCAAATCAATCCA | 8453 |
rs34740379 | in-del | -/T | 0.207253 | 0.246318 | intron-variant | CUL2 | GRCh38.p7 | 10:35055742 | TACAAGATCATACTC[-/T]TTTTTTTCCCCTTTA | 8453 |
rs34781602 | in-del | -/T | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125716 | GAATGAAAATTTTTT[-/T]GTGGACCTGCTGTAA | 8453 |
rs34834763 | in-del | -/G | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075338 | TAATAACATTCAGGG[-/G]AAAGTTTACACAAGG | 8453 |
rs34841370 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075061 | TGCACAGACTTTTTT[-/T]GCTTTATGGAATCAG | 8453 |
rs34890131 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014804 | CACCACTGCACTCCA[-/A]CCTGGGTGGCACAGC | 8453 |
rs34918025 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35023704 | GACAGATATTCATGG[-/G]AAAGTAAAAGCAAGC | 8453 |
rs34921285 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | CUL2 | GRCh38.p7 | 10:35102363 | GATAACTTGAGGCCA[A/G]GAGTTCAAGACCAGC | 8453 |
rs34954932 | snp | G/T | 0.44755 | 0.153212 | intron-variant | CUL2 | GRCh38.p7 | 10:35121879 | TTTTAAATAATTCAG[G/T]AGCTTGGGTTTTTAT | 8453 |
rs35011745 | in-del | -/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35029064 | TTGTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 8453 |
rs35028347 | in-del | -/AA | 0.412249 | 0.190198 | intron-variant | CUL2 | GRCh38.p7 | 10:35083155 | GCAAGACTCCATCTC[-/AA]AAAAAAAAAAAAAGA | 8453 |
rs35032841 | snp | A/G | 0.441841 | 0.160303 | intron-variant | CUL2 | GRCh38.p7 | 10:35023759 | TTAGTTTTCTTAGGG[A/G]AAAAAAAAAAAATCT | 8453 |
rs35059084 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35039493 | GAATCTAATTATTTT[-/C]ACGTTGGTTTCTCTT | 8453 |
rs35070038 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093370 | AGGCCATTTTTACTT[-/T]GAAAGAACAATTGAC | 8453 |
rs35096339 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35045362 | GGAGGCCAAGGTGGG[-/G]AGGATCCCTGAGTGC | 8453 |
rs35136660 | snp | A/C | 0.406123 | 0.195258 | intron-variant | CUL2 | GRCh38.p7 | 10:35097045 | GAACTCCTGTCTCCA[A/C]ATGACCCGTCCACCT | 8453 |
rs35151461 | in-del | -/A | 0.471578 | 0.115772 | intron-variant | CUL2 | GRCh38.p7 | 10:35068110 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 8453 |
rs35194641 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35101359 | TACCATTGTAGAAAA[-/A]TGTGGAGACCACACT | 8453 |
rs35210019 | multinucleotide-polymorphism | CA/TG | | | intron-variant | CUL2 | GRCh38.p7 | 10:35055979 | GACACACCTTTCAGG[CA/TG]TGCCCTGAACCCCAG | 8453 |
rs35223623 | in-del | -/A/AA | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35045561 | AAAAAAAAAAAAAAA[-/A/AA]CAACTTAGCTGTGCA | 8453 |
rs35238396 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093382 | CTTGAAAGAACAATT[-/T]GACAGACTTGGTGGC | 8453 |
rs35275515 | in-del | -/A/AA | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35018781 | AAAAAAAAAAAAAAA[-/A/AA]GATTTTAAAGGCTAT | 8453 |
rs35321888 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076409 | GAATGGTATGTGACG[-/G]TATATCTCAATAAAG | 8453 |
rs35332961 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123806 | CTGTCAGGTGTTTGG[-/C]AAATGTGACCTGGTG | 8453 |
rs35342564 | in-del | -/T | 0.148661 | 0.22854 | intron-variant | CUL2 | GRCh38.p7 | 10:35086185 | GACTGAGAGACTCTG[-/T]CTCAAAAAAAAAAAA | 8453 |
rs35355632 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35013490 | AAATACAACAAAACC[-/C]ATACCCTTTTCCTTA | 8453 |
rs35356037 | multinucleotide-polymorphism | AT/GC | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35093888 | AATCCTTTTCCTCTG[AT/GC]CAAATTTTTTTTATT | 8453 |
rs35360773 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35110211 | GCTATAGGAACAAGG[-/G]AGGTATAATTGTTGG | 8453 |
rs35427253 | in-del | -/AT | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009211 | TATATTATATATATA[-/AT]TATATATATAAAATA | 8453 |
rs35508150 | in-del | -/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35027162 | TTTTTTTTTTTTTTT[-/T]GAGGCGGAGTCTCGC | 8453 |
rs35517562 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35015459 | TGTCAGCAAAATGAA[-/A]TTAATGAGAGAAATA | 8453 |
rs35593131 | in-del | -/C | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074746 | CCGCCTTGGCCTCCC[-/C]AAAGTGCTGGGATTA | 8453 |
rs35593540 | in-del | -/T | 0.417196 | 0.185864 | intron-variant | CUL2 | GRCh38.p7 | 10:35021263 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTGAGA | 8453 |
rs35615779 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036401 | TACTATGAACATTCC[-/C]TGTATGTCTTTTTGT | 8453 |
rs35687560 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | CUL2 | GRCh38.p7 | 10:35035386 | AGGAGTACAATATAC[A/G]GATCCAAGTGCAGAG | 8453 |
rs35705723 | snp | G/T | 0.204803 | 0.245881 | intron-variant | CUL2 | GRCh38.p7 | 10:35010741 | AAGTTTTCCCCAGCA[G/T]CCCCTAGGCCAGGAT | 8453 |
rs35725384 | snp | G/T | 0.205417 | 0.245993 | intron-variant | CUL2 | GRCh38.p7 | 10:35024050 | ATGTTGCCCAGGCTG[G/T]TCTCAAACTCCTGGG | 8453 |
rs35726072 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35054143 | GTCCCCTGCACTTTT[-/T]AACTACAGGGCCGTC | 8453 |
rs35746562 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35116423 | CTCTGAAAGGCATAA[-/G]ACTACAAAACTTACT | 8453 |
rs35777088 | snp | C/T | 0.40733 | 0.194287 | intron-variant | CUL2 | GRCh38.p7 | 10:35120120 | GATTTATTTTATCAT[C/T]TAAATGATCATTTCC | 8453 |
rs35784065 | snp | C/T | 0.418169 | 0.184985 | intron-variant | CUL2 | GRCh38.p7 | 10:35064646 | ACATTTATTTACTTA[C/T]TTATAAATTTTTTAT | 8453 |
rs35790831 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078423 | CCTCAGCCTCCCAAG[-/C]TAGCTGGAATTACAG | 8453 |
rs35807819 | snp | C/T | 0.205723 | 0.246048 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091598 | GGTTAACAACTAGTT[C/T]GTTAACAATGCAATA | 8453 |
rs35809404 | in-del | -/T | 0.43221 | 0.171171 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128527 | GTTTTTTTCCTAGTC[-/T]TTTTTTTTTTTTTTT | 8453 |
rs35841309 | in-del | -/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35115723 | CATAGTGACACCCCC[-/C]ATCACTACAAAAAAA | 8453 |
rs35886556 | snp | C/T | 0.418007 | 0.185132 | intron-variant | CUL2 | GRCh38.p7 | 10:35046057 | TAGAGTCCTTCCCTG[C/T]CTCTGAACCCCTCTA | 8453 |
rs35896200 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128706 | ATTTTTTGTATTTTT[-/T]AGTAGAAACGGGGTT | 8453 |
rs35899911 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071020 | AACAAATACTTGTTG[-/G]AATGAAAGGTTATCA | 8453 |
rs35912711 | snp | C/T | 0.441841 | 0.160303 | intron-variant | CUL2 | GRCh38.p7 | 10:35024068 | TCAAACTCCTGGGAT[C/T]AAGTGACCCACCTGT | 8453 |
rs35917421 | snp | C/T | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075349 | CAGGGAAAGTTTACA[C/T]AAGGATGTGAAAGAG | 8453 |
rs35938164 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35035414 | AGCACCCAGAGAAAA[-/AA]GTCCCCCATGCCCAC | 8453 |
rs35997236 | snp | C/T | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35087762 | ACTTGTACCTTAACC[C/T]TCCACAGCCACTGCT | 8453 |
rs36074609 | in-del | -/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094843 | AAAATTCTTTCTGGG[-/G]TAACCCTTTAAGTTA | 8453 |
rs36082710 | in-del | -/A | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35127080 | GGGGCCGCTGCCGGC[-/A]TCCGGGTTGCTGGGC | 8453 |
rs36123879 | snp | G/T | 0.412416 | 0.190055 | intron-variant | CUL2 | GRCh38.p7 | 10:35106984 | TTTGTTTGTTTGTTT[G/T]TTTGTTTTGAGGCAG | 8453 |
rs36124097 | in-del | -/T | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35039428 | AACAGGTGATCTCTG[-/T]TATGAATAACTATCA | 8453 |
rs41276098 | snp | C/T | 0.0369835 | 0.130878 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35074176 | TGCCCTTATCAAAGA[C/T]ACAAAAATAACCTAC | 8453 |
rs45555138 | snp | A/T | 0.00517822 | 0.0506191 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008457 | GTAGACCTCCGCACA[A/T]GTATTTTGTCCATTT | 8453 |
rs55643354 | in-del | -/TTATTTAT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119609 | TATTTATTTATTTAT[-/TTATTTAT]AGAGACAGGGTCTCA | 8453 |
rs55712040 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076709 | TCATCTGTTTTACAT[A/G]AATGGTATACTATTC | 8453 |
rs55798281 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076592 | GACCTCATTGCCACC[C/T]CCCATTGAATGAGGC | 8453 |
rs55807054 | snp | C/G | 0.269267 | 0.249256 | intron-variant | CUL2 | GRCh38.p7 | 10:35068222 | AGCCCAGGGGTTCGA[C/G]ACCAGCTTGGCCAAC | 8453 |
rs55835800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35037797 | ATAGTGAACAGAGAT[C/T]GCGCCACTGCATTAT | 8453 |
rs55863836 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35083667 | AAGGTCAAAACTGGA[A/C]CAAATCAGAGCAACA | 8453 |
rs55920660 | snp | C/T | 0.277867 | 0.248442 | intron-variant | CUL2 | GRCh38.p7 | 10:35040052 | CAGCTACTCGGGAGG[C/T]TGAGGCAGAAGAACT | 8453 |
rs55960106 | snp | A/G | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35040726 | AATTTTTCCACAGAC[A/G]GAGTGCGGGCGGCAT | 8453 |
rs56140666 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35107910 | AAAAAAAAAAAAAAA[-/A]GTAGAAGACCTGGTT | 8453 |
rs56154331 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35076481 | ATTTTAGAGCAATTT[A/G]ACGGGGATGAGGTGG | 8453 |
rs56743909 | snp | A/G | 0.205417 | 0.245993 | intron-variant | CUL2 | GRCh38.p7 | 10:35015250 | GTGAGCCAAGATCAC[A/G]CCATTGCACTCCACC | 8453 |
rs56776632 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075676 | CACACACACACACAC[-/AC]GCACGCTCCACATTT | 8453 |
rs56919928 | snp | A/G | 0.206029 | 0.246103 | intron-variant | CUL2 | GRCh38.p7 | 10:35073674 | CAATGGCGCAATCTC[A/G]GCTCACTGCAACCTC | 8453 |
rs57785229 | snp | A/C | 0.213635 | 0.247341 | intron-variant | CUL2 | GRCh38.p7 | 10:35089818 | ATGAGATGCCCCCCC[A/C]CACACACACACACAA | 8453 |
rs57786297 | snp | C/T | 0.467946 | 0.122472 | intron-variant | CUL2 | GRCh38.p7 | 10:35073697 | GCAACCTCTGCTTCC[C/T]GGGTTGAAGTGATTC | 8453 |
rs57819230 | snp | C/G | 0.0618563 | 0.164627 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075411 | CACTATTTCTACCCC[C/G]CAAGCTGTCAAACAA | 8453 |
rs57901385 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CUL2 | GRCh38.p7 | 10:35116082 | GCACAGCGGTTCACA[C/T]CTGTAATCCCAGCAC | 8453 |
rs57996012 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35082148 | GAAAAAAAAAAAAAA[-/A]TTTGCCTGCAGTGAG | 8453 |
rs58015167 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | CUL2 | GRCh38.p7 | 10:35078839 | TTATTTCAGTACTGA[C/T]CAGCAGCACCAATAA | 8453 |
rs58058299 | in-del | -/AT/ATTATA/TA | 0.499928 | 0.00598999 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009201 | TATATATATATATAT[-/AT/ATTATA/TA]TATATATATATATAT | 8453 |
rs58159560 | snp | C/T | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35062321 | AGACTTCATATAGCA[C/T]ATGAAAGGCAGCTAA | 8453 |
rs58275497 | in-del | -/T | | | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091634 | GTCCTTTTTTTTTTT[-/T]GGATACAGAGTCTTG | 8453 |
rs58512444 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | CUL2 | GRCh38.p7 | 10:35070061 | TGTGGTCCATCAATT[A/G]CTACCCGTATGACCC | 8453 |
rs58582764 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093681 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAGA | 8453 |
rs58779572 | in-del | -/A | 0.039241 | 0.134464 | intron-variant | CUL2 | GRCh38.p7 | 10:35025203 | AATAATTCAAACTGT[-/A]AAAAAAAAAAAAAAA | 8453 |
rs58799123 | in-del | -/TATTT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35122643 | TATTTTATTTTATTT[-/TATTT]ATTTATTTTTTTGAG | 8453 |
rs58899384 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35108177 | GTGACAGTAGTTTGG[C/G]CCAGGCACAGTGGCT | 8453 |
rs58902254 | in-del | -/T | 0.0941726 | 0.195494 | intron-variant | CUL2 | GRCh38.p7 | 10:35049631 | ACTATTTTAAAACCA[-/T]TATCAAACAACAAAA | 8453 |
rs58923870 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CUL2 | GRCh38.p7 | 10:35085431 | CGAGACACCGTCCCA[A/G]AAAAAAATAAAAATA | 8453 |
rs59042466 | in-del | -/CAAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35046931 | CAAAACAAAACAAAA[-/CAAAA]ACAAAAAACTGGGTT | 8453 |
rs59269668 | in-del | -/G | 0.0887219 | 0.191022 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009513 | AGACAACTTTTGAAT[-/G]GAAAAGCTCTCTCTG | 8453 |
rs59418206 | snp | A/G | 0.40595 | 0.195396 | intron-variant | CUL2 | GRCh38.p7 | 10:35042696 | GACCTTCCCTTATGT[A/G]TCTCCTCAAGTGGTT | 8453 |
rs59502768 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35099863 | AAGTAAGCCAAAAGA[A/G]AAAAAGAAAAAAATG | 8453 |
rs59518617 | in-del | -/AAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113528 | AAAAAAAAAAAAAAA[-/AAA]TTCCGCAAGATCCAG | 8453 |
rs59621927 | snp | C/T | 0.206029 | 0.246103 | intron-variant | CUL2 | GRCh38.p7 | 10:35073861 | TCCACCCACCTTGGC[C/T]TCCCAAAGTGCTAGG | 8453 |
rs59814360 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090552 | ATCCGTAAAACAATC[G/T]TCCTCCTCTGCCTCC | 8453 |
rs59858482 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35089998 | GGGCTTACGGGTCAG[C/T]GCTCTGGGGAGCCGA | 8453 |
rs59866726 | in-del | -/A | 0.342582 | 0.232225 | intron-variant | CUL2 | GRCh38.p7 | 10:35020167 | ATAGAAAACAAATTT[-/A]AAAAAAAAAAAAATA | 8453 |
rs59891080 | snp | A/G | 0.0193772 | 0.0965046 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126373 | CAGCTGTGACTGGCT[A/G]TGAATATGGAGGAAA | 8453 |
rs59923574 | in-del | -/CTTTTT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35073614 | TTTCTTTTTCTTTTT[-/CTTTTT]TTTTTTGAGATGGAG | 8453 |
rs60181547 | in-del | -/ACAAA | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35123181 | ACAAAACAAAACAAA[-/ACAAA]GGACTTCATGCCAAA | 8453 |
rs60540282 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018469 | TGTATTCATTACCTC[A/T]TTAAAGATTTTAGGC | 8453 |
rs60598982 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CUL2 | GRCh38.p7 | 10:35039809 | GTAACGAGCCAAGAT[C/T]GCACCACTGCACTCC | 8453 |
rs60648958 | snp | C/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35094360 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGATTA | 8453 |
rs60698057 | snp | G/T | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35024870 | AATACATTTGCTAAT[G/T]AAGTGGTTGGCTAGA | 8453 |
rs60753509 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123173 | AAAAACAAAACAAAA[A/C]AAAACAAAGGACTTC | 8453 |
rs60779322 | in-del | -/ACACACACACACACAC | | | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075668 | CACACACACACACAC[-/ACACACACACACACAC]GCACGCTCCACATTT | 8453 |
rs60845094 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | CUL2 | GRCh38.p7 | 10:35065731 | AGGTGTGGTGGCACA[C/T]GCCTGTAATGCCAGC | 8453 |
rs60895044 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35096709 | ATAAGAGTATTTCAA[A/C]GGGGCACAGGAGCCA | 8453 |
rs61014969 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | CUL2 | GRCh38.p7 | 10:35095003 | TTTATTTAATTCCTT[C/T]ATAATTGTTTCTGAC | 8453 |
rs61022194 | in-del | -/AA | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35038550 | AAAAAAAAAAAAAAA[-/AA]TCAGATATAGCTGAT | 8453 |
rs61066279 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075176 | AAATCTGGAAGCCAA[C/T]GTGCAAGAAGCACCA | 8453 |
rs61100854 | in-del | -/T | 0.434253 | 0.168969 | intron-variant | CUL2 | GRCh38.p7 | 10:35020964 | TTTTTATTTTATGGG[-/T]TTTTTTTTTTTTTTT | 8453 |
rs61104795 | snp | C/T | 0.4444 | 0.15719 | intron-variant | CUL2 | GRCh38.p7 | 10:35073753 | GAGATTACAGGCGTC[C/T]GCCACCACACCCGGC | 8453 |
rs61161332 | snp | C/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35093129 | ACACCCCTATGATTC[C/T]ATCCCCAACCCATCA | 8453 |
rs61290598 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | CUL2 | GRCh38.p7 | 10:35011084 | ATTTATTATTATCAT[C/T]TGAGATAGCATCTCA | 8453 |
rs61291084 | snp | G/T | 0.270621 | 0.249148 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126148 | AAAAAAAAAAGAGAT[G/T]AAGTCTCACTGTGTT | 8453 |
rs61371614 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35096867 | CAGGCTGGAGTGCAG[G/T]GGTGCAATCTCAGCT | 8453 |
rs61373878 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | CUL2 | GRCh38.p7 | 10:35053121 | TGTGTGTTTATGTAA[A/G]TATTTATAAATACAC | 8453 |
rs61398539 | in-del | -/ATCGC/CGC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35030823 | CTTGAGCCCAGGAGT[-/ATCGC/CGC]TAGAGTCCAGCCTGG | 8453 |
rs61467648 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35047608 | AGCAAGACTGTCTCA[-/A]AAAAAAAAAAAAAAA | 8453 |
rs61540590 | in-del | -/ATTT | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080480 | TTTATTTATTTATTT[-/ATTT]TTGAGACAGGGTCTT | 8453 |
rs61749171 | snp | C/T | 0.00887866 | 0.0660341 | missense | CUL2 | GRCh38.p7 | 10:35033271 | CACAAATAGTGTTGG[C/T]ATCTAAAAATGAAAT | 8453 |
rs61754549 | snp | A/T | 2.0595e-05 | 0.0032089 | missense | CUL2 | GRCh38.p7 | 10:35013763 | TTACTGCTAAAGTTC[A/T]TATTTAATGAAAACG | 8453 |
rs61841046 | snp | C/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009342 | TGATGAGAGTGACTC[C/T]AGTATCTAAACTGTT | 8453 |
rs61841047 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CUL2 | GRCh38.p7 | 10:35013213 | AGCCAGGCATAGTGG[C/T]GGGCGCCTGTAGTCC | 8453 |
rs61841048 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35020961 | TTCTTTTTATTTTAT[G/T]GGTTTTTTTTTTTTT | 8453 |
rs61841049 | snp | A/G | 0.444444 | 0.157135 | intron-variant | CUL2 | GRCh38.p7 | 10:35021707 | ACCTCAGCCTCCCAA[A/G]TAGCTGGGACTACAG | 8453 |
rs61841050 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021920 | GTGGGGCGAAGTGGG[A/G]CGAGGGGGCACCCGG | 8453 |
rs61841051 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35026946 | CCACTAACTCGTCAT[G/T]TAGCATTAGGTATAT | 8453 |
rs61841052 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35040878 | TGTGAGAATCTATGA[C/G/T]AATCTAATGCTGCTG | 8453 |
rs61841053 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35061459 | AGCAAGACTCTGTCT[A/C]CCAAAAAAAAAAAAA | 8453 |
rs61841054 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062690 | AAAAAAAAAAAAAAT[A/T]GCCAGGTGTGGTGGT | 8453 |
rs61841055 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077468 | TGCCACTGCACTCCA[C/G]TCTGGACAACAGAGC | 8453 |
rs61841056 | snp | A/C/T | 0.434253 | 0.168969 | intron-variant | CUL2 | GRCh38.p7 | 10:35092891 | AAAGTGTAGGCATAT[A/C/T]TCTATTAATATACTC | 8453 |
rs61841057 | snp | A/T | 0.435119 | 0.16802 | intron-variant | CUL2 | GRCh38.p7 | 10:35092892 | AAGTGTAGGCATATT[A/T]CTATTAATATACTCC | 8453 |
rs61841058 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35094339 | CTCCCAGGTTCAAGC[G/T]ATTCTCCTGCCTCAG | 8453 |
rs61841059 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119546 | TATAATTTTTAGGGA[G/T]GTTTTAAAATTAATT | 8453 |
rs66476226 | in-del | -/TTT | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35018312 | CATGTTGATTTCATC[-/TTT]TTTTTTTTTTTGTTT | 8453 |
rs66578882 | in-del | -/GTGTGT | 0 | 0 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075678 | AAATGTGGAGCGTGC[-/GTGTGT]GTGTGTGTGTGTGTG | 8453 |
rs66620544 | snp | C/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35096202 | TCAGTGAGTTGAGAT[C/T]TTGCCACTCCAGCAT | 8453 |
rs66887762 | snp | C/T | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35041649 | CTCAAGTGATCTTCC[C/T]ACCTCAGCGTCCCAA | 8453 |
rs66943310 | in-del | -/T | 0.0648419 | 0.167978 | intron-variant | CUL2 | GRCh38.p7 | 10:35033757 | CTTTTTTTTTTTTTT[-/T]GTTGTTGTTGTTGTT | 8453 |
rs67257350 | in-del | -/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35103309 | TTTTTTTTTTTTTTT[-/T]ATTTTTTTTTGAGAC | 8453 |
rs67261877 | snp | A/T | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35097412 | GAAGGATTGCTTGAG[A/T]TCAGGAGATTGAGAT | 8453 |
rs67460702 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35089820 | GTTTGTGTGTGTGTG[-/T]GGGGGGGGGCATCTC | 8453 |
rs67976880 | snp | C/G | 0.406123 | 0.195258 | intron-variant | CUL2 | GRCh38.p7 | 10:35083333 | AACACACATATACAT[C/G]CAGATAAAAAGATAT | 8453 |
rs68039650 | snp | A/C | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35096571 | TGAGCTGTGATTATG[A/C]CACTGCACTACAGAC | 8453 |
rs71033374 | in-del | -/TTT | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35093679 | TCTTCTTTTCTTTTC[-/TTT]TTTTTTTTTTTTTTT | 8453 |
rs71033375 | in-del | -/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35096250 | AGCTGTTTTGTTTTG[-/T]TTTTTTTCTTTTCTG | 8453 |
rs71033377 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35114826 | TCCAATGTATTTTTT[-/T]ATTTCAGACCTTGCA | 8453 |
rs71299708 | in-del | GAA/TGTGT | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35092893 | GGGAGTATATTAATA[GAA/TGTGT]ATATGCCTACACTTT | 8453 |
rs71485998 | in-del | CA/GCCTCCCAG | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35088431 | CTCACTGCAACCTCC[CA/GCCTCCCAG]GTTCAAGCAATTCTC | 8453 |
rs71485999 | in-del | -/AAGCGATC/TAA | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35030823 | GCCCAGGCTGGACTC[-/AAGCGATC/TAA]CTCCTGGGCTCAAGC | 8453 |
rs71487384 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35018298 | TCTCACAAAAAAAAA[A/C]AAAAAAAAAAAAAAA | 8453 |
rs71487385 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35018303 | CAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAGATG | 8453 |
rs71487386 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35025807 | ATAAAGAGCTAGTAT[A/C]CAATAAAAAGTGGAA | 8453 |
rs71487387 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35038357 | GGTGAAACCCTGTCT[C/T]TACTAAAAGTACAAA | 8453 |
rs71487388 | snp | A/C/G | 1.93661e-05 | 0.0031117 | intron-variant | CUL2 | GRCh38.p7 | 10:35049641 | AAACCATATCAAACA[A/C/G]CAAAATAAAATTGAC | 8453 |
rs71487389 | snp | C/T | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35058052 | GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC | 8453 |
rs71487390 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35077024 | ACTCCCAAGAGAAAT[A/C]CAACATATTCACATA | 8453 |
rs71487391 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35078114 | TACTAACCTTCCCTT[C/T]TGAGAATCTTAACTT | 8453 |
rs71523352 | in-del | -/AAA | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35013361 | AAAAAAAAAAAAAAA[-/AAA]TGAACTGGAGAACTT | 8453 |
rs71523353 | in-del | -/A | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35023771 | GGGAAAAAAAAAAAA[-/A]TCTAAAACCCTGGTC | 8453 |
rs71523355 | in-del | -/A | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35050338 | AAAAAAAAAAAAAAA[-/A]CTTAATTTTTTGATT | 8453 |
rs71523356 | in-del | -/A | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35067158 | AAAAAAAAAAAAAAA[-/A]GAAATGAAGACAACA | 8453 |
rs71523358 | in-del | -/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35096827 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCAC | 8453 |
rs71523359 | in-del | -/A | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35097492 | AAAAAAAAAAAAAAA[-/A]GAACTTACAGTGGTG | 8453 |
rs71660665 | in-del | -/A | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113182 | CAAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 8453 |
rs71973671 | in-del | -/CAAAACAAAA | 0.453209 | 0.145623 | intron-variant | CUL2 | GRCh38.p7 | 10:35046892 | AGTGAGACTCTGTCT[-/CAAAACAAAA]CAAAACAAAACAAAA | 8453 |
rs71976816 | in-del | -/AAAAC | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123159 | GCAAAACATAACAAA[-/AAAAC]AAACAAAACAAAACA | 8453 |
rs72052501 | in-del | -/ATTT | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080441 | TCCTATTTTTATTTA[-/ATTT]TTTATTTATTTATTT | 8453 |
rs72330362 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35018764 | CGAAACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 8453 |
rs72351187 | in-del | -/CT/TC | 0.375 | 0.216506 | intron-variant | CUL2 | GRCh38.p7 | 10:35054270 | CATCTTTTTCGTTCC[-/CT/TC]TGAGGATTCTTAGGA | 8453 |
rs72412550 | in-del | -/CC | 0.398354 | 0.201224 | intron-variant | CUL2 | GRCh38.p7 | 10:35089811 | AGGATGCATGAGATG[-/CC]CCCCCCCACACACAC | 8453 |
rs72789609 | snp | C/T | 0.418007 | 0.185132 | intron-variant | CUL2 | GRCh38.p7 | 10:35017278 | GAAAGGAGAGACAAA[C/T]AGGCAGACCCATTCT | 8453 |
rs72789615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35035855 | ACAGCTGCCAACAGC[A/G]GAGAGTTCCTTTGCC | 8453 |
rs72789685 | snp | A/T | 0.208474 | 0.246527 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081447 | GAAACTGACATTTTT[A/T]AAAAAAACTATTCTC | 8453 |
rs72789687 | snp | A/G | 0.406123 | 0.195258 | intron-variant | CUL2 | GRCh38.p7 | 10:35083561 | GGAAAAATACAAGTT[A/G]AACCTAGAACACCTA | 8453 |
rs72789688 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091287 | ATTCAGCAAGCTTTT[C/T]CCTCCCATCCCTTCC | 8453 |
rs72789689 | snp | A/G | 0.206029 | 0.246103 | intron-variant | CUL2 | GRCh38.p7 | 10:35093888 | AATCCTTTTCCTCTG[A/G]TCAAATTTTTTTTAT | 8453 |
rs72789690 | snp | C/T | 0.405776 | 0.195535 | intron-variant | CUL2 | GRCh38.p7 | 10:35093889 | ATCCTTTTCCTCTGA[C/T]CAAATTTTTTTTATT | 8453 |
rs72789691 | snp | A/C | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35094203 | ATACAATAGATATAA[A/C]CCACATGAACATAAG | 8453 |
rs72789693 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35095338 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAATACA | 8453 |
rs72791807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35121097 | TGGGAGCTACTTAAC[A/G]CATTCCCCATAATGT | 8453 |
rs73256993 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35011790 | AAGAAAGAGACTGAA[A/T]CTGTACAATGACAAT | 8453 |
rs73256999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35019137 | TATTTCTGCAATGAC[A/G]ACTTAATCATATGCA | 8453 |
rs73257002 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35027875 | GGGAAACTAAAACCT[C/G]AGGAAGACTATACAT | 8453 |
rs73258711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35032049 | CACCTAGGTGAGTTT[C/T]GAGTGGTTTTATAAT | 8453 |
rs73258713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35034340 | TACAAAAAATAGAAA[A/G]CTGTGGTAAAGGGAA | 8453 |
rs73258727 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35042131 | TATTTTTCATTACCC[C/T]ATCAGAAACTTTATA | 8453 |
rs73258730 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35042535 | ATCTTGCCCTACCTT[C/T]CTGACTGTGGGTCAT | 8453 |
rs73258735 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35046799 | CAGGAGGCTGAGGTA[A/G]GAAAATTGGCTTGAA | 8453 |
rs73258758 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | CUL2 | GRCh38.p7 | 10:35056854 | ACATCAGAATCACTT[A/G]TCTCATCCTTCCATT | 8453 |
rs73258759 | snp | A/C | 0.0577344 | 0.159793 | intron-variant | CUL2 | GRCh38.p7 | 10:35057783 | AATCAAATTTATTAA[A/C]CACATATTTGCTTCT | 8453 |
rs73258776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074947 | GGACAATTCTGTAAC[C/T]GCGTACCAAAAAGCT | 8453 |
rs73258789 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | CUL2 | GRCh38.p7 | 10:35078647 | GTGAACTCACTTGCT[A/G]GAGCAAAAAAACAAT | 8453 |
rs73258791 | snp | A/G | 0.0681886 | 0.171594 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079471 | AATGCTTTCTGGCAC[A/G]GTATGTTGCCATCAA | 8453 |
rs73258798 | snp | G/T | 0.0681886 | 0.171594 | intron-variant | CUL2 | GRCh38.p7 | 10:35084833 | CTTAAAAACAACTGA[G/T]AGTTGGACAGGCCTG | 8453 |
rs73260804 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35089426 | GGTAGGCTTGGCCAG[A/G]TCTAGTTCAAAGACG | 8453 |
rs73260807 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35093197 | TCCATAAAAACCCCA[A/G]CCTCCAACCCAGGGG | 8453 |
rs73260824 | snp | C/G | 0.067446 | 0.170804 | intron-variant | CUL2 | GRCh38.p7 | 10:35106258 | CCTTCACCAGACACA[C/G]CTTGATCTTGGACTT | 8453 |
rs73260828 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35111289 | TCGGGTTCTGGTTCT[A/G]TTGCCCAACTGGAGT | 8453 |
rs73260829 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | CUL2 | GRCh38.p7 | 10:35112380 | AAAGGGAAAACAGAG[A/G]TGACTCCTACAATTG | 8453 |
rs73260832 | snp | C/G | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35114720 | TTTTATAAATATACA[C/G]TATATGTTCACAAAA | 8453 |
rs73260834 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35116492 | ATCTATTGTTTCTCT[C/T]TGATGATGTTTAATT | 8453 |
rs73260837 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35117036 | AGACATTTCTTCCAC[C/G]CTTACAATGAAAAAA | 8453 |
rs73260847 | snp | G/T | 0.0681886 | 0.171594 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126922 | GATTTTTTTCCTCGG[G/T]GCCTCCCCCGGGAGG | 8453 |
rs74132496 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CUL2 | GRCh38.p7 | 10:35060578 | AGTTGAATTTTCACA[C/T]TGATCTCTGTTGAGA | 8453 |
rs74132498 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | CUL2 | GRCh38.p7 | 10:35109619 | GCAAGGAGAGGCCAG[C/T]CCCACAAACATTTGC | 8453 |
rs74343938 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CUL2 | GRCh38.p7 | 10:35030682 | ACCACCACACCTGGC[C/G]AACACTACTTTTAGA | 8453 |
rs74366253 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35020035 | TGACATTAGATGCCT[C/T]TGAAATATGCAATAT | 8453 |
rs74402978 | snp | A/G | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35086190 | AGAGACTCTGTCTCA[A/G]AAAAAAAAAAGAAAC | 8453 |
rs74424550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35016038 | TCTGTGATGCCTTAA[C/T]GCTCGCAGCTCTATG | 8453 |
rs74440587 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35017693 | ATGAGTATCTGTCTC[A/C]AAAAAAAAAAAAAAA | 8453 |
rs74458015 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35018300 | TCACAAAAAAAAAAA[A/C]AAAAAAAAAAAAAAG | 8453 |
rs74491371 | snp | A/G | 0.444444 | 0.157135 | intron-variant | CUL2 | GRCh38.p7 | 10:35124104 | GGGAGGATCGCTTTA[A/G]ACTAGGTACTTGAAG | 8453 |
rs74508187 | in-del | -/AT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021519 | TTCCATAATTAATAC[-/AT]GTTTATATTAATGTC | 8453 |
rs74546120 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | CUL2 | GRCh38.p7 | 10:35095699 | GAGTAGCTGGAACTA[A/C]AGGCACATGCCAATA | 8453 |
rs74563015 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021811 | TGGGGTGAGGAGAGG[C/T]GAGGTGGGGTGAGGT | 8453 |
rs74575402 | snp | A/C | 0.409721 | 0.192325 | intron-variant | CUL2 | GRCh38.p7 | 10:35077330 | AAACAAACAAACAAA[A/C]AAAAAAAACAAACAA | 8453 |
rs74617125 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021808 | AGGTGGGGTGAGGAG[A/G]GGCGAGGTGGGGTGA | 8453 |
rs74712298 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CUL2 | GRCh38.p7 | 10:35012232 | CAAATTATATAGTTA[C/T]GTTGTGCCAATATCA | 8453 |
rs74745297 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35020084 | TATGAAATATCCTTG[A/C]CAATAATACTTAACT | 8453 |
rs74779402 | snp | C/T | 0.0295035 | 0.117819 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074563 | CAGGCTCGAGTGCAC[C/T]GCAACCTCCACCTCC | 8453 |
rs74838538 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35052894 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAGAA | 8453 |
rs74842166 | snp | A/G | 0.255224 | 0.249945 | intron-variant | CUL2 | GRCh38.p7 | 10:35097172 | GATTTACTGAGCACC[A/G]ACTAAAGTGTCACAA | 8453 |
rs74935348 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119281 | CTGTTTTCATTGGTT[C/T]AGTTATTTTATCTTA | 8453 |
rs74982317 | snp | A/G | 0.205723 | 0.246048 | intron-variant | CUL2 | GRCh38.p7 | 10:35102224 | TGGGTGACAGAGCGA[A/G]ACTCCATCTCAAAAA | 8453 |
rs74989280 | snp | A/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35050625 | CAATCCACAATTTTG[A/T]GAAACCCATCCAGTG | 8453 |
rs74994869 | snp | A/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021422 | AAACATACATTTTTT[A/T]ATATATGTATGTATA | 8453 |
rs75059137 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021456 | ATACACACACACACA[C/T]ACATACACACACACA | 8453 |
rs75115307 | snp | A/G | 0.275575 | 0.248688 | intron-variant | CUL2 | GRCh38.p7 | 10:35036465 | AGCTGGGGGGTGGTT[A/G]TATGTTTAGGAGAAC | 8453 |
rs75282588 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35061468 | CTGTCTCCCAAAAAA[A/C]AAAAAAAAAATCACA | 8453 |
rs75341902 | snp | A/C | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35025218 | AAAAAAAAAAAAAAA[A/C]CACACATTATTTTTA | 8453 |
rs75346430 | in-del | -/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35069567 | AATTAAAAAAAAAAA[-/AA]GGATAACTAAACCAT | 8453 |
rs75366845 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | CUL2 | GRCh38.p7 | 10:35071394 | CATGAGCTTAGTTTT[G/T]TTGTTGTTGTTTTTT | 8453 |
rs75371692 | snp | A/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35106485 | CCACCACGCCCGGCT[A/T]ATTTTTTTTTTTCTT | 8453 |
rs75435624 | snp | G/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35054940 | AAATGCAATTTTTCA[G/T]TTTTAAACAAAAAAG | 8453 |
rs75439536 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021460 | ACACACACACATACA[C/T]ACACACACACAAATA | 8453 |
rs75455150 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | CUL2 | GRCh38.p7 | 10:35066103 | TTTCATGTTCTCTAT[C/T]AAAAGGTGTTTCCTA | 8453 |
rs75525371 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35063751 | CGGGTGGCATTTCCT[C/T]TTTTTTTTTTTTTTT | 8453 |
rs75606358 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35019992 | TCATCAAGTGACCAA[A/G]TTTAGCATCTCTAAT | 8453 |
rs75729742 | snp | A/C | 0.270621 | 0.249148 | intron-variant | CUL2 | GRCh38.p7 | 10:35119255 | AAGGCTCAGTTTCAG[A/C]TTCAAAGTACCTGTT | 8453 |
rs75745412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35082544 | CTATACCCTTAATGA[C/T]GGTTAAAATGGTAAA | 8453 |
rs75747881 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021476 | ACACACACACAAATA[C/T]GTAGTGATAAAACTA | 8453 |
rs75752586 | snp | C/T | 0.270621 | 0.249148 | intron-variant | CUL2 | GRCh38.p7 | 10:35109136 | GAGGATTGCTTGAGC[C/T]TGGAGGTTGAGGCTC | 8453 |
rs75783845 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35056946 | ACTTCCTTTGACTTC[C/T]AATCTACTTGCTGAC | 8453 |
rs75797430 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35047905 | GTGGGAATCCTGTCT[A/C]AAAAAAAAAAAGGAA | 8453 |
rs75800770 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35121809 | AGTAAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 8453 |
rs75806191 | snp | G/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35026446 | TTAAAAAAACTTTCA[G/T]TTTTTTCTCAAAACA | 8453 |
rs75823043 | snp | A/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35119536 | CTAGGTATACTATAA[A/T]TTTTAGGGAGGTTTT | 8453 |
rs75846617 | snp | A/C | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021475 | TACACACACACAAAT[A/C]TGTAGTGATAAAACT | 8453 |
rs75886007 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CUL2 | GRCh38.p7 | 10:35067637 | TAATCCCAGCTACAC[A/G]GGAGGATGAGGCATG | 8453 |
rs75993612 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35067142 | AAAACTCCATCTCAA[A/C]AAAAAAAAAAAAAAA | 8453 |
rs76020716 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35112361 | AGGACTGTGATCCCC[A/G]AGCAAAGGGAAAACA | 8453 |
rs76042717 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35093043 | ACCCCACCTGGACTC[A/G/T]TGACTCATGACTCAG | 8453 |
rs76203075 | snp | C/T | 0.5 | 0 | missense | CUL2 | GRCh38.p7 | 10:35028827 | TCTGTACACTTTTTT[C/T]TAATTCCTGGGGAAT | 8453 |
rs76233833 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35012259 | ATCACATAACCACTG[C/T]TAAAACATCTACAAT | 8453 |
rs76239096 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021676 | CTGCCTGGTCTTCTC[A/T]CTCTGGGCTCTGGTG | 8453 |
rs76255521 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021474 | ATACACACACACAAA[C/T]ATGTAGTGATAAAAC | 8453 |
rs76258975 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35017692 | AATGAGTATCTGTCT[A/C]AAAAAAAAAAAAAAA | 8453 |
rs76360383 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021493 | TAGTGATAAAACTAT[A/G]TAGATGATATTTCCA | 8453 |
rs76587172 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CUL2 | GRCh38.p7 | 10:35056229 | CAAAAAATAATTACT[A/G]AATAAATAAATGGAT | 8453 |
rs76604997 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021793 | ACTCCAGCTTACGTG[A/G]GGTGGGGTGAGGAGA | 8453 |
rs76606916 | snp | G/T | 0.021333 | 0.101051 | intron-variant | CUL2 | GRCh38.p7 | 10:35098010 | AATAAAAGAACAAAA[G/T]TACAAGGTCTTTAAT | 8453 |
rs76667642 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021750 | CCCGGGAGGCAGAGG[C/T]TAATGTGGGCTGTGA | 8453 |
rs76701277 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | CUL2 | GRCh38.p7 | 10:35033732 | ACAGAGTGAGACTCC[G/T]TCTCAGAAAAACAAC | 8453 |
rs76756627 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CUL2 | GRCh38.p7 | 10:35051478 | ATTAGCCGGGCGAGG[C/T]GGCGGGCGCCTGTAG | 8453 |
rs76800194 | snp | A/G | 0.270351 | 0.24917 | intron-variant | CUL2 | GRCh38.p7 | 10:35062089 | AGTGAAGATTCTTAC[A/G]CAGGCACTAAATTAT | 8453 |
rs76920058 | snp | C/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35043317 | ACAAAAGTCTAAGGT[C/G]CAATAAGGGCTAAGA | 8453 |
rs76947303 | snp | A/G | 0.0165278 | 0.0893908 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126334 | GTCTCAGGAGCTCAA[A/G]CTTCTTTTGGAGAAG | 8453 |
rs77006330 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35018295 | CCATCTCACAAAAAA[A/C]AAAAAAAAAAAAAAA | 8453 |
rs77021681 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021774 | GCTGTGATCGCGCAC[C/T]TCCACTCCAGCTTAC | 8453 |
rs77025207 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35073550 | CCAACATTCTGACAG[C/G]TAGGTCCACTGTTGT | 8453 |
rs77083517 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | CUL2 | GRCh38.p7 | 10:35041922 | ACACCTTGAGATGTA[A/G]TTTACATATTAAATA | 8453 |
rs77122725 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021586 | CATTTCATTTACATA[C/T]ACATGTATATCCTTC | 8453 |
rs77128955 | snp | C/T | 0.269605 | 0.24923 | intron-variant | CUL2 | GRCh38.p7 | 10:35082468 | AAGTTTTGGAAATGG[C/T]GGTTTTGGAAATGGT | 8453 |
rs77148354 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35069568 | ATTAAAAAAAAAAAA[A/G]GGATAACTAAACCAT | 8453 |
rs77153390 | snp | G/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35073617 | TCTTTTTCTTTTTTT[G/T]TTTGAGATGGAGTCT | 8453 |
rs77212639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35040590 | AGTCCTGTCTTTCCT[A/G]TTGTGCGACCCTTTG | 8453 |
rs77215464 | snp | C/T | 0.270621 | 0.249148 | intron-variant | CUL2 | GRCh38.p7 | 10:35120962 | AAGGTAATATGGATA[C/T]AATTCCCTTATGTTT | 8453 |
rs77217724 | snp | C/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021798 | AGCTTACGTGAGGTG[C/G]GGTGAGGAGAGGCGA | 8453 |
rs77231340 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078197 | TACTGTCCCTAAATG[A/T]GATGTGTTAACATAG | 8453 |
rs77234417 | snp | C/T | 0.270351 | 0.24917 | intron-variant | CUL2 | GRCh38.p7 | 10:35111408 | AGGTGTGCACCACCA[C/T]GCCTAACTAAGATTT | 8453 |
rs77317162 | in-del | -/AAAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35093678 | AAAAAAAAAAAAAAA[-/AAAA]GAAAAGAAAAGAAGA | 8453 |
rs77456053 | snp | C/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021744 | CTTAAGCCCGGGAGG[C/G]AGAGGCTAATGTGGG | 8453 |
rs77565138 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35069207 | AGACTTTTTATTTTG[G/T]GGGTGAGAGAAAATT | 8453 |
rs77585666 | snp | C/T | 0.268452 | 0.249318 | intron-variant | CUL2 | GRCh38.p7 | 10:35058513 | CTAAAGTCTAGTTCC[C/T]AAAACCTAAGGTCTG | 8453 |
rs77598809 | snp | A/G | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35047916 | GTCTCAAAAAAAAAA[A/G]GGAAAAAAGGACAGG | 8453 |
rs77599679 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35019697 | CAGGAAATAAAGAGC[A/G]GGCAGAACTCTCACA | 8453 |
rs77651007 | snp | G/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35058006 | GGGAGGCTGAGGCAG[G/T]AGAATGGTGTGAACC | 8453 |
rs77730154 | snp | A/G | 0.277867 | 0.248442 | intron-variant | CUL2 | GRCh38.p7 | 10:35106053 | GTTCCCCCAAAATTC[A/G]TATGTTGAAACCTAA | 8453 |
rs77756801 | snp | A/C | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35099387 | AAAGTGAGACTCCGT[A/C]TAAAAAAAAAAAAAA | 8453 |
rs77761878 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021410 | ACTGCTGTGTATAAA[C/T]ATACATTTTTTTATA | 8453 |
rs77794779 | snp | G/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35020964 | TTTTTATTTTATGGG[G/T]TTTTTTTTTTTTTTT | 8453 |
rs77853239 | in-del | -/AAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35062686 | AAAAAAAAAAAAAAA[-/AAA]TTGCCAGGTGTGGTG | 8453 |
rs78011574 | snp | G/T | 0.269538 | 0.249235 | intron-variant | CUL2 | GRCh38.p7 | 10:35042307 | CATAACATTTTCATG[G/T]TTCATCCATGTTGTA | 8453 |
rs78069681 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35012616 | AAGAGGATCTCCTCA[C/T]AGCGTTTCAAAGACA | 8453 |
rs78136174 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | CUL2 | GRCh38.p7 | 10:35082015 | TTACAATCCCAAAGA[A/G]AGCCAGTGAGTTGGA | 8453 |
rs78180885 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35052895 | GCGAGACTCCGTCTC[A/C]AAAAAAAAAAAGAAA | 8453 |
rs78208559 | snp | C/T | 0.254385 | 0.249962 | intron-variant | CUL2 | GRCh38.p7 | 10:35093654 | AATAAAGGCAGACCT[C/T]CTCTCAAAAAAAAAA | 8453 |
rs78259841 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021813 | GGGTGAGGAGAGGCG[A/G]GGTGGGGTGAGGTGA | 8453 |
rs78263878 | in-del | -/T | | | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009878 | TTCTTTATTTTTTTT[-/T]TATTTGACAAGCAGC | 8453 |
rs78328775 | snp | A/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35020602 | TGGTGAAGTTTTTTT[A/T]ATCTTCCTTGAGTTC | 8453 |
rs78361755 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021675 | CCTGCCTGGTCTTCT[C/G]ACTCTGGGCTCTGGT | 8453 |
rs78384347 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021473 | CATACACACACACAA[A/C]TATGTAGTGATAAAA | 8453 |
rs78387412 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021682 | GGTCTTCTCACTCTG[C/G]GCTCTGGTGACCTCA | 8453 |
rs78419371 | snp | G/T | 0.268995 | 0.249277 | intron-variant | CUL2 | GRCh38.p7 | 10:35107502 | GGACACAGAAATGTG[G/T]CCTTTAATGTTGTTG | 8453 |
rs78435243 | snp | A/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35106487 | ACCACGCCCGGCTAA[A/T]TTTTTTTTTTCTTTT | 8453 |
rs78438602 | in-del | -/AAA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35033769 | AACAAAAAAAAAAAA[-/AAA]GGAAGAAAGAAAATA | 8453 |
rs78585312 | snp | A/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35063769 | TTTTTTTTTTTTTTA[A/T]TATCCTTTGCTTTAT | 8453 |
rs78611367 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35069528 | CCTGGGTGACAAAGT[C/G]AGACCCTGTCTCTAA | 8453 |
rs78614297 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35105707 | AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAGAA | 8453 |
rs78620025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35014481 | AAAGGCACTTGGAAG[A/G]TGAAATAATTCTCAA | 8453 |
rs78637942 | snp | C/T | 0.5 | 0 | missense | CUL2 | GRCh38.p7 | 10:35028826 | ATCTGTACACTTTTT[C/T]CTAATTCCTGGGGAA | 8453 |
rs78643776 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021496 | TGATAAAACTATATA[A/G]ATGATATTTCCATAA | 8453 |
rs78798139 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35024841 | GTGTCTGCCCCATCA[A/G]ATGTGAGTTTCTAAA | 8453 |
rs78817015 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35037466 | AGTCTTTCCATCATA[A/C]TCTTCAAGACAGTGA | 8453 |
rs78897609 | snp | A/G | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35051652 | TAGTGTCTCCTTGTG[A/G]TTTTAACTCTCATTT | 8453 |
rs78898531 | snp | A/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021423 | AACATACATTTTTTT[A/T]TATATGTATGTATAT | 8453 |
rs79026659 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35123499 | AATAAAAAAAAAAGG[A/G]ATGGATGCAAGTTTC | 8453 |
rs79035143 | snp | A/G | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35089731 | TAGCATGCACGTAGG[A/G]TACTCCTCCCCAAAG | 8453 |
rs79083074 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021754 | GGAGGCAGAGGCTAA[C/T]GTGGGCTGTGATCGC | 8453 |
rs79111276 | snp | A/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35017875 | TGTTCCATACGTGTT[A/T]AAAAAAAAAAAAAAA | 8453 |
rs79175004 | snp | G/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35106569 | AATCTCCTGACCTCA[G/T]GATCCGCCCACCTCG | 8453 |
rs79175415 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CUL2 | GRCh38.p7 | 10:35062088 | GAGTGAAGATTCTTA[C/T]GCAGGCACTAAATTA | 8453 |
rs79184721 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35072373 | GTGAACTTAATGGGC[C/T]TTTTTTTTTTTTTGA | 8453 |
rs79233083 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35061460 | GCAAGACTCTGTCTC[A/C]CAAAAAAAAAAAAAA | 8453 |
rs79273990 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021770 | GTGGGCTGTGATCGC[A/G]CACCTCCACTCCAGC | 8453 |
rs79340497 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35078196 | GTACTGTCCCTAAAT[G/T]TGATGTGTTAACATA | 8453 |
rs79368293 | snp | C/T | 0.030665 | 0.119967 | intron-variant | CUL2 | GRCh38.p7 | 10:35034668 | GATTGGCAAAGTATT[C/T]GAGAAAGATGAGTAT | 8453 |
rs79384319 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CUL2 | GRCh38.p7 | 10:35034815 | GGCAAATTGCAAGTC[A/G]TCTATATTACCACTG | 8453 |
rs79389709 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021803 | ACGTGAGGTGGGGTG[A/G]GGAGAGGCGAGGTGG | 8453 |
rs79392837 | snp | C/G | 0.254385 | 0.249962 | intron-variant | CUL2 | GRCh38.p7 | 10:35058945 | GAGTTAGGGGGTCAA[C/G]ACTTCAGGGGAGGAA | 8453 |
rs79414218 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021472 | ACATACACACACACA[A/C]ATATGTAGTGATAAA | 8453 |
rs79436062 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35015295 | TGGAACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 8453 |
rs79523600 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126141 | ATCTAAAAAAAAAAA[-/AA]GAGATGAAGTCTCAC | 8453 |
rs79526604 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35015293 | AGTGGAACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 8453 |
rs79583411 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CUL2 | GRCh38.p7 | 10:35030153 | CACAGCTGCTGGCTC[C/T]TATAAGGTTTACAGA | 8453 |
rs79593805 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35019876 | TTAGGTTCCTGGAAC[A/G]GGGTATTCATGCCAA | 8453 |
rs79657867 | snp | A/G | 0.270621 | 0.249148 | intron-variant | CUL2 | GRCh38.p7 | 10:35122750 | TCAAGTGGTTCTCAT[A/G]CCTCGGGCTCTTAAG | 8453 |
rs79684422 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35121811 | TAAGACCCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 8453 |
rs79714044 | snp | G/T | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35073277 | AGGGGAAGGTGAGAG[G/T]GGAGGAGGTGGGAGA | 8453 |
rs79716010 | snp | A/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35063767 | TTTTTTTTTTTTTTT[A/T]AATATCCTTTGCTTT | 8453 |
rs79754287 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35015404 | ATGCCTTTTACAGTT[A/G]TTCAGTTATAGACTA | 8453 |
rs79883197 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35121595 | AATGTGGCATGGAGC[C/G]CTTTTCCAATATGAA | 8453 |
rs79909279 | snp | A/C | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35067139 | AGCAAAACTCCATCT[A/C]AAAAAAAAAAAAAAA | 8453 |
rs79934294 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | CUL2 | GRCh38.p7 | 10:35012794 | TTATCTTCACATCCT[C/G]CATCAGCCCAAGGAC | 8453 |
rs79968538 | snp | A/T | 0.00663032 | 0.0571944 | intron-variant | CUL2 | GRCh38.p7 | 10:35025083 | TTTCTAAATTAATAT[A/T]ATCATCAGGTAAATT | 8453 |
rs79974597 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35115994 | GATAAAAATTACCAA[C/G]ATTTGGCTTGAAAGA | 8453 |
rs79983062 | snp | G/T | 0.0551013 | 0.156571 | intron-variant | CUL2 | GRCh38.p7 | 10:35119102 | CTTTTATCTAACATT[G/T]GATGGAGTCTCTCTG | 8453 |
rs79992941 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CUL2 | GRCh38.p7 | 10:35024228 | AATTAGAATGTCCAA[C/T]TTGCTCAGTAAAGAT | 8453 |
rs80009025 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35084961 | TCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGACG | 8453 |
rs80019110 | in-del | -/TTTT | | | intron-variant | CUL2 | GRCh38.p7 | 10:35063764 | CTTTTTTTTTTTTTT[-/TTTT]AATATCCTTTGCTTT | 8453 |
rs80044555 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35093102 | AGGCTCAGCACTCAA[C/G]GACTGTTTTCCACAC | 8453 |
rs80051769 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35036629 | ATTGGCCATCTGGGT[A/G]TCTTCTATTCTGCAG | 8453 |
rs80088103 | snp | A/T | 0.0174175 | 0.0916809 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008555 | AAAAAAAGGAATCAA[A/T]TTGGAAAACTTTTAT | 8453 |
rs80133611 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35013344 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 8453 |
rs80152043 | snp | A/G | 0.029116 | 0.117091 | intron-variant | CUL2 | GRCh38.p7 | 10:35082460 | TAACGAAAAAGTTTT[A/G]GAAATGGTGGTTTTG | 8453 |
rs80173842 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CUL2 | GRCh38.p7 | 10:35026004 | AAAAAGGAAGTTCAC[A/T]TAAAGCAGTCAGCAA | 8453 |
rs80292140 | snp | C/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021795 | TCCAGCTTACGTGAG[C/G]TGGGGTGAGGAGAGG | 8453 |
rs111226391 | snp | C/T | 0.254664 | 0.249956 | intron-variant | CUL2 | GRCh38.p7 | 10:35107265 | AGGCATGAGCCACCG[C/T]GCCCAGCTGCCCTTA | 8453 |
rs111245197 | in-del | -/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35106951 | AACCTGTTTTTTTTT[-/T]GTTGTTTTTTTGTTT | 8453 |
rs111259829 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | CUL2 | GRCh38.p7 | 10:35011701 | TGAAATTGTGAGTGA[A/G]TACGATTCTGATTAA | 8453 |
rs111267338 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CUL2 | GRCh38.p7 | 10:35116849 | GTAGTCCCAGCTACC[C/T]GGGAGGCTGAGGTGG | 8453 |
rs111272722 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35124913 | TATTTTCTCAGAAAA[C/G]TAGGTGACCTAGTTG | 8453 |
rs111279725 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021604 | ATGTATATCCTTCCT[C/T]CCTTCCTTCTTTCAT | 8453 |
rs111292287 | snp | G/T | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35110105 | ACTTGAGCCTGGGAG[G/T]TCAAGGCTGCAGTGA | 8453 |
rs111309597 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35097917 | TGAGCCACAATCATG[C/T]CACTGCACTCCAGCC | 8453 |
rs111361483 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021614 | TTCCTTCCTTCCTTC[A/T]TTCATTTATTATTTT | 8453 |
rs111417142 | snp | C/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35033123 | GCCTAAAGAATGATA[C/G]AGTTTTATGTACATA | 8453 |
rs111437395 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35039746 | TGTAATCCCAGCTCC[C/T]TGGGAGGCCAGGGCA | 8453 |
rs111456749 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | CUL2 | GRCh38.p7 | 10:35034858 | ACCATGACAACAAAC[C/T]ACGTTATCAATGCCA | 8453 |
rs111461522 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35063381 | AATCCTACAAAATAA[C/G]GTTTATATTAGAATG | 8453 |
rs111473896 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35067711 | ATCACACCACTGCAC[C/T]CCAACCTGGGCAACA | 8453 |
rs111476259 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35068026 | GAGGCAGGAGAATGG[C/T]ATGAACCCGGGAGGC | 8453 |
rs111497293 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35123033 | GTCCTAGCTACTCAG[A/G]AGGCTGAGGTGGGAG | 8453 |
rs111521883 | in-del | -/CT | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35016918 | GGTGACAGAGCGAGA[-/CT]CTGTCTCAAAAAAAA | 8453 |
rs111561555 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35020007 | ATTTAGCATCTCTAA[C/T]AGTGAGACAATCTGA | 8453 |
rs111613185 | snp | A/G | 0.275197 | 0.248727 | intron-variant | CUL2 | GRCh38.p7 | 10:35011233 | TTTTTTTTTTTTTTT[A/G]GGTGAGATGGGGTCT | 8453 |
rs111617297 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CUL2 | GRCh38.p7 | 10:35062386 | GAGATAGGAATAAAA[A/G]ACGAGGGAAAATTTG | 8453 |
rs111637201 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35050488 | ATTTTATACCAACAT[A/G]AAAAGAGCAAGTCGG | 8453 |
rs111666761 | in-del | -/G | 0.467946 | 0.122472 | intron-variant | CUL2 | GRCh38.p7 | 10:35057810 | TCTTAATAAAGACAT[-/G]GGGCTGGACGCAGTG | 8453 |
rs111717119 | in-del | -/CTCA | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35070765 | TCTAATGTCACCATC[-/CTCA]CTCAGGGAGGCCTTC | 8453 |
rs111729154 | snp | C/T | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35095652 | CAACCTCCGCCTCCC[C/T]GGTTCAAGCCATTCT | 8453 |
rs111732123 | snp | C/T | 0.268995 | 0.249277 | intron-variant | CUL2 | GRCh38.p7 | 10:35099174 | GAGGAGGGCAGATCA[C/T]GAGGTCAGGAGATCC | 8453 |
rs111736536 | snp | C/T | 0.207253 | 0.246318 | intron-variant | CUL2 | GRCh38.p7 | 10:35104966 | ATTCCCGACCTCAGA[C/T]GATCCACCCGCCTGG | 8453 |
rs111818410 | snp | A/G | 0.089084 | 0.191327 | intron-variant | CUL2 | GRCh38.p7 | 10:35041317 | GGGAGAGAGAGGCGC[A/G]TATCAAGAGAAATGT | 8453 |
rs111821310 | snp | A/C | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35025366 | CACGTTCCTGTGGTC[A/C]CTAATCAAGGCTATA | 8453 |
rs111822105 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CUL2 | GRCh38.p7 | 10:35073524 | ACCCTGTACAAACTC[A/G]TTTAATCCTCCCAAC | 8453 |
rs111824688 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021836 | TGAGGTGAGGCGAGG[C/T]GAGGTGAGGTGAGGT | 8453 |
rs111830739 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35112869 | TTTTAAAAGGATCTA[A/G]CTGATTTCAAGTACT | 8453 |
rs111853057 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35102329 | GCAATCCCAACACTT[C/T]GGGAAGCCAAGGCAG | 8453 |
rs111869338 | snp | C/T | 0.00952816 | 0.0683615 | intron-variant | CUL2 | GRCh38.p7 | 10:35031252 | GAACATCTTTATGTG[C/T]TTGTGAATGAATTTC | 8453 |
rs111869437 | in-del | -/A | 0.441841 | 0.160303 | intron-variant | CUL2 | GRCh38.p7 | 10:35023758 | TTAGTTTTCTTAGGG[-/A]GAAAAAAAAAAAATC | 8453 |
rs111879405 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35065449 | CATGGTGAAACCCCA[C/T]CTCTACTAAAACACA | 8453 |
rs111881291 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | CUL2 | GRCh38.p7 | 10:35069584 | GGATAACTAAACCAT[A/G]TTAGATGGACCAAAC | 8453 |
rs111911338 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35025026 | GGAAAGGTTGATGGA[A/G]GAGAAAAGGTTAAAA | 8453 |
rs111943046 | snp | A/G | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35128794 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 8453 |
rs111965616 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35011206 | GCTAATTTTTTAATT[G/T]TTTAATTTTTTTTTT | 8453 |
rs111965838 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021877 | GGGGTGGGGTGAGGT[C/G]GGGTGAGGTGGGGTG | 8453 |
rs111972815 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | CUL2 | GRCh38.p7 | 10:35030970 | CCTGCTACCACTTAT[C/G]GGTATGTAAGCAAGC | 8453 |
rs111979498 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35058083 | AGCCGGGGAAACAGC[A/G]AGACTCGGTCCCAAA | 8453 |
rs111986474 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | CUL2 | GRCh38.p7 | 10:35101512 | AGCTACAATGAAGAC[G/T]TAAGTGATGGAAGTG | 8453 |
rs111988480 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CUL2 | GRCh38.p7 | 10:35117898 | TAGACTTGATTTTTT[C/T]CAGAACAATTTTAGG | 8453 |
rs111994488 | snp | C/G | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125854 | TTTATTTTTGAGATG[C/G]AGCCTCGCTCTGTCA | 8453 |
rs111998154 | snp | C/T | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35076866 | ATCAGCTGGCTGACA[C/T]GGTGAAACCCCATCT | 8453 |
rs112022615 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | CUL2 | GRCh38.p7 | 10:35107620 | TGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 8453 |
rs112029366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35019142 | CTGCAATGACGACTT[A/C]ATCATATGCAGAAAT | 8453 |
rs112030411 | snp | A/G | 0.089084 | 0.191327 | intron-variant | CUL2 | GRCh38.p7 | 10:35026019 | ATAAAGCAGTCAGCA[A/G]TGACTGACCTATCAG | 8453 |
rs112103431 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35057122 | GTAAACTGCCTAGCA[C/G/T]AGAAGCAGATGCTAA | 8453 |
rs112112839 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35094008 | AAATTTTTATCCTTT[A/G]AATTTCTAATACAAT | 8453 |
rs112114104 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35078106 | AAAGCCGTTACTAAC[A/C]TTCCCTTCTGAGAAT | 8453 |
rs112118504 | in-del | -/A | 0.172351 | 0.237636 | intron-variant | CUL2 | GRCh38.p7 | 10:35105827 | AGAGGCAATGTCCTG[-/A]AAAAAAAAAAAAAAA | 8453 |
rs112135522 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35045500 | GGGATGATCCCTTGA[A/G]TCCTGAGTTTGAGAC | 8453 |
rs112144020 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | CUL2 | GRCh38.p7 | 10:35053969 | TCAGCATAATTTTCC[A/G]TATTTTAATTTGCAC | 8453 |
rs112146515 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35117885 | TTTGTTTTCTTAATA[A/G]ACTTGATTTTTTTCA | 8453 |
rs112186161 | in-del | -/C | 0.029116 | 0.117091 | intron-variant | CUL2 | GRCh38.p7 | 10:35013389 | CTTTCCCTTATTTTA[-/C]AAATGAAAAATATGA | 8453 |
rs112247988 | snp | C/T | 0.444444 | 0.157135 | intron-variant | CUL2 | GRCh38.p7 | 10:35117180 | AGGGCACTAGCTTAC[C/T]TGGGACAGACACAAC | 8453 |
rs112254130 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CUL2 | GRCh38.p7 | 10:35089106 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 8453 |
rs112255245 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | CUL2 | GRCh38.p7 | 10:35026567 | TGTTTTACCTCTTCA[G/T]TAGTACTATTTGGTA | 8453 |
rs112265052 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080055 | TGAAATTTTCCATTT[A/C]ATATTTGCAGACCCC | 8453 |
rs112275238 | in-del | -/A | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35047905 | TGGGAATCCTGTCTC[-/A]AAAAAAAAAAAGGAA | 8453 |
rs112281580 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35100582 | GCCTGGCCAACATGG[C/T]GAAACCTCGTCTCTA | 8453 |
rs112294875 | snp | A/G | 0.5 | 0 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35031509 | TTGAAAGACGTCCTT[A/G]TCATCAATGTATTTG | 8453 |
rs112296753 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35060376 | AGATGGGAGAGACCA[C/T]GGGCCATTAGGAAAC | 8453 |
rs112346261 | snp | G/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35107022 | CTCTGTCACCCAGAG[G/T]AGAGTGCAGTGGCAT | 8453 |
rs112355429 | snp | C/G | 0.444444 | 0.157135 | intron-variant | CUL2 | GRCh38.p7 | 10:35092991 | AACATCAGTATTGTA[C/G]AACTTTAGATTGCTT | 8453 |
rs112376420 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35047818 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 8453 |
rs112403518 | snp | A/T | 0.269267 | 0.249256 | intron-variant | CUL2 | GRCh38.p7 | 10:35105558 | AAAAAATACAAAAAA[A/T]TTTGCCGGGTGTGGT | 8453 |
rs112405923 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35071467 | TGGAGTGCAATGGCG[C/T]GATCTTGGCTCACTG | 8453 |
rs112414553 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021266 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTGAGACGG | 8453 |
rs112443055 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CUL2 | GRCh38.p7 | 10:35017491 | TTAAACCCAGGAGTT[C/T]GAGACCAGCCTGGTC | 8453 |
rs112452437 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35096552 | CAGGAGGTCATGTTT[A/G]CAGTGAGCTGTGATT | 8453 |
rs112472353 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35012693 | AAATGGAATCTTGAC[A/C]ATTTTAGGTTTCAAA | 8453 |
rs112503832 | snp | C/T | 0.444444 | 0.157135 | intron-variant | CUL2 | GRCh38.p7 | 10:35062791 | GCAGTGAGCCATGAT[C/T]GCGCCACTGCACCCT | 8453 |
rs112516169 | in-del | -/A | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35082135 | ACATCATCTTGACTG[-/A]AAAAAAAAAAAAATT | 8453 |
rs112534332 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35053035 | AAAAAAGGCAAGAAA[C/T]ATAGGCTGTAGAACT | 8453 |
rs112540516 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CUL2 | GRCh38.p7 | 10:35037627 | AAGGCAGGTGGATCA[C/T]GAGCTCAGGAGTTCG | 8453 |
rs112540936 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35044685 | GATAAAACTGAATAA[A/G]TCAATTACATCATAT | 8453 |
rs112549254 | in-del | -/GTGT | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021588 | TTCATTTACATATAC[-/GTGT]CATGTATATCCTTCC | 8453 |
rs112549710 | in-del | -/T | 0.465158 | 0.127307 | intron-variant | CUL2 | GRCh38.p7 | 10:35094239 | CTAAGTCCTCGATAA[-/T]TTTTTTTTTTTTTGA | 8453 |
rs112555222 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35025529 | TATAAATTCTACTAA[C/T]CAAACACAGCAACAT | 8453 |
rs112555885 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35113262 | GCATTTTGGGAGCCC[A/G]AGGTGGGTGGATCAC | 8453 |
rs112613808 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35066670 | GCATTAGCAAACAAG[C/G]ATAAAAAATGACTAA | 8453 |
rs112713975 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CUL2 | GRCh38.p7 | 10:35058564 | GTCGATTCTTAGCTG[A/G]TAATTCCCAGGCACA | 8453 |
rs112749151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35120745 | TACGAAAAATACAAA[A/C]ATTAGCCTGGCATGG | 8453 |
rs112760667 | snp | C/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35071518 | CACGCCATTCTCCTG[C/T]CTCAGTCTCCCAAGT | 8453 |
rs112768609 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35115319 | GTAATCCCAGCACTT[C/T]GGGAGGCGGAGGCGG | 8453 |
rs112774051 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35081704 | TTCGCAGCCAACCTG[C/G]GCAACATGGTGAACC | 8453 |
rs112779776 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35089154 | CACTCCAGCCTGGGT[A/G]ACAAGAGCAAAACTC | 8453 |
rs112814219 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | CUL2 | GRCh38.p7 | 10:35062109 | CACTAAATTATCTCA[G/T]CCAGTTCCTGATTAG | 8453 |
rs112847858 | in-del | -/T | 0.306927 | 0.243432 | intron-variant | CUL2 | GRCh38.p7 | 10:35114083 | TGGCTAATTTTTGGG[-/T]TTTTTTTTTTTGGTA | 8453 |
rs112876478 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | CUL2 | GRCh38.p7 | 10:35052752 | TACAAAAAATTAGCC[A/G]GGTGTGGTGGCAGGC | 8453 |
rs112896557 | snp | A/C | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35083039 | GCAGGTGCCTGTAAT[A/C]CCAGCTACTCAGGAG | 8453 |
rs112934719 | snp | A/T | 0.0681886 | 0.171594 | intron-variant | CUL2 | GRCh38.p7 | 10:35051437 | GCTAACATAGTGAAA[A/T]CCCGTCTCTACTAAA | 8453 |
rs113007471 | snp | A/C | | | intron-variant | CUL2 | GRCh38.p7 | 10:35014778 | GTGGGGATTGCAGTG[A/C]GCTGAGATGGCACCA | 8453 |
rs113018497 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | CUL2 | GRCh38.p7 | 10:35106420 | CGCCTCTCAGGTTCA[C/T]GCCATTCTCCTGCCT | 8453 |
rs113019197 | snp | A/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35031932 | AAACTAAATAAAATA[A/T]ACATCATAAGGTAAA | 8453 |
rs113023156 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | CUL2 | GRCh38.p7 | 10:35017576 | GCATATGCCTGTAAA[C/T]CCAGCTACTCGGGAG | 8453 |
rs113044028 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35069485 | GGTTGAGGCTGCAGT[A/G]AGCTATAGTCACACC | 8453 |
rs113052031 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35065229 | TATGACTTGATTATA[A/G]ACAAGACACTTTAAA | 8453 |
rs113055358 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075045 | AAATTAGTTTAACAG[C/T]TGCACAGACTTTTTT | 8453 |
rs113067461 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35047181 | ATTTTAAATATCAGG[A/G]ATTCTATTCACTGTA | 8453 |
rs113096840 | snp | C/T | 0.268724 | 0.249298 | intron-variant | CUL2 | GRCh38.p7 | 10:35057700 | TCACAATTTAAAATA[C/T]AAACAGTGCCATTTT | 8453 |
rs113132237 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35058499 | TCCAGATCTGTAGTC[C/T]AAAGTCTAGTTCCTA | 8453 |
rs113171877 | in-del | -/CA | 0 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35021455 | ATACACACACACACA[-/CA]TACATACACACACAC | 8453 |
rs113186734 | snp | A/G | 0.5 | 0 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35044865 | GTCTTCTCCACCACG[A/G]TCACTAAAACAAGGT | 8453 |
rs113214187 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | CUL2 | GRCh38.p7 | 10:35104198 | ACACCTGTAATCCCA[A/G]CACTTACGGATGCCG | 8453 |
rs113214373 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35081536 | ACTAGGCAAGCCCAT[C/T]GTGTATGAATACTAG | 8453 |
rs113233884 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091188 | CATATATGCAGGGCC[A/G]CAGAGGAACAAAAGC | 8453 |
rs113258045 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35034288 | AAGTTTGACAAATAA[C/T]AGAGTAATAAACCTG | 8453 |
rs113279918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35084178 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATCAC | 8453 |
rs113327213 | snp | A/G | 0.5 | 0 | splice-donor-variant | CUL2 | GRCh38.p7 | 10:35031489 | TTCTGTTCACAACAT[A/G]CCTTTTGAAAGACGT | 8453 |
rs113362965 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35037305 | CTGCCGCTCTGCAGC[A/G]CCACCTTGGTCTTAC | 8453 |
rs113387953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35099110 | CAATAATATTAACTT[A/G]GGCTGGGTGCATTGG | 8453 |
rs113399769 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | CUL2 | GRCh38.p7 | 10:35087706 | AACATGACAATTTCA[A/G]TAAGTATCTTCAACT | 8453 |
rs113468459 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35098797 | AAATTAGCTGGGCAC[A/G]GTGGCAGGCGCCTGT | 8453 |
rs113490254 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CUL2 | GRCh38.p7 | 10:35047426 | CCATCCTGGCTAAAA[C/T]GGTGAAACCCCGTCT | 8453 |
rs113505201 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | CUL2 | GRCh38.p7 | 10:35034632 | GACAAACTGTTACAG[G/T]ACAAACTGTTACAGT | 8453 |
rs113559022 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | CUL2 | GRCh38.p7 | 10:35061140 | TGAAACAACTGGGAA[A/G]GATGTGAGTCTTCAA | 8453 |
rs113563130 | snp | C/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35113957 | CTGTCGCTCAGGCTG[C/G]AGTGCAGTGGCATGA | 8453 |
rs113575976 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35050501 | ATAAAAAGAGCAAGT[C/T]GGTTAAAAGAGTAAT | 8453 |
rs113642404 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35011717 | TACGATTCTGATTAA[G/T]TATGAAACATTTCTT | 8453 |
rs113646696 | snp | A/T | 0.5 | 0 | downstream-variant-500B | CUL2 | GRCh38.p7 | 10:35008532 | TTTAACATTTATAAA[A/T]ATTTAAGAAAAAAAG | 8453 |
rs113667555 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127855 | CATTATTAAACATAC[-/T]TTTTTTTTTTGAGAC | 8453 |
rs113681739 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35098729 | TGAGGTCAGGAGTTC[A/G]AGACCAACCTGGCCA | 8453 |
rs113702552 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | CUL2 | GRCh38.p7 | 10:35105500 | TCCCGCACTTTGGGA[A/G]GGAGACCATCCTGGC | 8453 |
rs113713122 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | CUL2 | GRCh38.p7 | 10:35029720 | ATAATGTGTCGGTAT[A/T]GCTAGGTCTTTGATC | 8453 |
rs113757608 | snp | A/G | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35124678 | GTTTTCAAGAGGCAC[A/G]ATACTAACACATTTG | 8453 |
rs113765112 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077214 | TGGATGACCCTCAAA[A/G]ACATTCTACTAAGTG | 8453 |
rs113790271 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075247 | GAAGGTATGCTGAGA[C/G]AGTCTGTCAAGATTC | 8453 |
rs113807591 | in-del | -/A | 0.0887219 | 0.191022 | intron-variant | CUL2 | GRCh38.p7 | 10:35054063 | TTTTAAAGTAAAGTT[-/A]ACAATAAATTTGTTG | 8453 |
rs113828261 | snp | A/C/T | 0.0655868 | 0.168795 | intron-variant | CUL2 | GRCh38.p7 | 10:35054182 | ATAATTGTTTCTGAG[A/C/T]TTTTTCACAATGCAG | 8453 |
rs113831439 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35094446 | CACCATGTTGGTCAG[A/G]CTGGTCTTGAACTCC | 8453 |
rs113877697 | snp | A/T | 0.0607341 | 0.163335 | intron-variant | CUL2 | GRCh38.p7 | 10:35088181 | CTGTCTGTCTCTCCA[A/T]CCCAAGCCAGAAGTG | 8453 |
rs113933281 | snp | C/T | 0.270892 | 0.249126 | intron-variant | CUL2 | GRCh38.p7 | 10:35120852 | AGCGAGCCAAGATCA[C/T]GCCACTGCAATCCAG | 8453 |
rs113948475 | snp | G/T | 0.5 | 0 | intron-variant | CUL2 | GRCh38.p7 | 10:35027827 | TTGGAATCAGAATTT[G/T]ACAGACAGAAACTCA | 8453 |
rs113964557 | in-del | -/AAAAC | 0.0842632 | 0.187929 | intron-variant | CUL2 | GRCh38.p7 | 10:35123158 | AGCAAAACATAACAA[-/AAAAC]AAAACAAAACAAAAC | 8453 |
rs113986429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35024060 | GGCTGGTCTCAAACT[C/T]CTGGGATTAAGTGAC | 8453 |
rs114078412 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35066981 | TTTGAAAGAGATGCC[C/T]GATAGAATATAAACT | 8453 |
rs114084189 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35060642 | AGAAACAGAGCCATG[C/T]AATCGAGTACAGTTT | 8453 |
rs114090409 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | CUL2 | GRCh38.p7 | 10:35106192 | CTCCCTCACTTCTTC[A/G]GTCATGTGAGGACAT | 8453 |
rs114103183 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35091267 | GGGTCTTGTTCATTT[A/G]TACGATTCAGCAAGC | 8453 |
rs114105072 | snp | A/G/T | 0.0182412 | 0.0940547 | intron-variant | CUL2 | GRCh38.p7 | 10:35084052 | AAGGCCAAAGAGGGC[A/G/T]GATCTCTTGAGGTCA | 8453 |
rs114116692 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | CUL2 | GRCh38.p7 | 10:35030183 | ATAGTATCAAATGAA[A/C]GATTACATAAATGAT | 8453 |
rs114130297 | snp | C/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118691 | CCCTCTGTGCTCATT[C/G]CTCATACTTATTCCT | 8453 |
rs114274254 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | CUL2 | GRCh38.p7 | 10:35123590 | CAAAATATTTTCTAT[C/G]TGGCTCCTGAATGAC | 8453 |
rs114283387 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35124824 | AAGAGGTGCTCCTCC[C/T]GACCCAGAAAGGGAG | 8453 |
rs114284349 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35034029 | AGACCCCTTGAACTC[A/G]GCAAGACAATCCCTC | 8453 |
rs114351678 | snp | C/T | 0.253824 | 0.249971 | intron-variant | CUL2 | GRCh38.p7 | 10:35024067 | CTCAAACTCCTGGGA[C/T]TAAGTGACCCACCTG | 8453 |
rs114412156 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090924 | GCCACACACTTCCAT[A/G]GGCTTTGCAAATGAT | 8453 |
rs114419125 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35024728 | TTGCATTCACTGCAG[C/T]ATCACAAGTAAAAAT | 8453 |
rs114421775 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35106232 | ACGACCATCTGTGAT[A/C]CACAGAGGGGCCTTC | 8453 |
rs114552717 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35057208 | CTTGAGCCAGGTATT[A/G]ATTTAGTGCAGCTTT | 8453 |
rs114557945 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35116421 | ATTCTCTGAAAGGCA[C/T]AAACTACAAAACTTA | 8453 |
rs114607033 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35112866 | AAATTTTAAAAGGAT[C/G]TAACTGATTTCAAGT | 8453 |
rs114688851 | snp | G/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021656 | TATTTATTTTCTTTT[G/T]GGGCCTGCCTGGTCT | 8453 |
rs114731270 | snp | C/T | 0.0681886 | 0.171594 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126939 | CCTCCCCCGGGAGGC[C/T]GTCCCGGCGTGGGGG | 8453 |
rs114743523 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CUL2 | GRCh38.p7 | 10:35124001 | GTGAAACCATGAGAG[C/T]CAAGTATCATGAAAA | 8453 |
rs114750952 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35042366 | ACTGTGTGGTGTTGT[A/G]ATATGTAAGTACATT | 8453 |
rs114754798 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35019239 | GCTGTAATATGCTGC[C/T]GTGGGTTTGAAAGCA | 8453 |
rs114764539 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CUL2 | GRCh38.p7 | 10:35066982 | TTGAAAGAGATGCCT[A/G]ATAGAATATAAACTA | 8453 |
rs114804428 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35058919 | AGTTAACACTTCCAA[C/T]CCTCATGGATGAGTT | 8453 |
rs114843396 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35117377 | AGTATTGGGACTATA[G/T]ATGAGTGCCACCATG | 8453 |
rs114940181 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | CUL2 | GRCh38.p7 | 10:35034076 | AAATACCTAATAGTA[A/C]AAAAGTGAGTTTTCC | 8453 |
rs114958082 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075408 | TCACACTATTTCTAC[A/C]CCCCAAGCTGTCAAA | 8453 |
rs115035131 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CUL2 | GRCh38.p7 | 10:35111748 | AAAAAATTAGCTGGG[C/T]GTGGTGTGGCATGTG | 8453 |
rs115115176 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | CUL2 | GRCh38.p7 | 10:35066433 | CTCCTGAGTAGCTGG[C/G]ATTACAGTTGAGCGC | 8453 |
rs115126992 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35082543 | ACTATACCCTTAATG[A/G]CGGTTAAAATGGTAA | 8453 |
rs115148655 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35012236 | TTATATAGTTATGTT[A/G]TGCCAATATCACATA | 8453 |
rs115173280 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CUL2 | GRCh38.p7 | 10:35118312 | CTTTCACATGTTCTT[C/T]TTTTCCCCTTCTGGA | 8453 |
rs115185022 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | CUL2 | GRCh38.p7 | 10:35061559 | CACTTATGGTGTTAA[A/C]CAAAGCTCACTAGCT | 8453 |
rs115192503 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | CUL2 | GRCh38.p7 | 10:35103811 | GTCAGTATGAACTAA[C/T]ATTGCTTTCATACTC | 8453 |
rs115201556 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35124161 | TACTCTAACCTGGGT[G/T]ACAGAGCGAGACTCT | 8453 |
rs115206759 | snp | A/C/G | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35042407 | TGTGGTTCCTGGTTC[A/C/G]TAACTCCCTTAGCCC | 8453 |
rs115253622 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CUL2 | GRCh38.p7 | 10:35029393 | GCCACAATCTACTCA[C/T]AGAACCAAACGTAAT | 8453 |
rs115271125 | snp | C/T | 0.00301267 | 0.0386944 | intron-variant | CUL2 | GRCh38.p7 | 10:35062956 | CGTATGTATCATTGC[C/T]TACCTTATGCAAATG | 8453 |
rs115446007 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CUL2 | GRCh38.p7 | 10:35082448 | GTTTCTGTCTAGTAA[C/T]GAAAAAGTTTTGGAA | 8453 |
rs115448436 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35121096 | TTGGGAGCTACTTAA[C/T]GCATTCCCCATAATG | 8453 |
rs115459802 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | CUL2 | GRCh38.p7 | 10:35037003 | TAATGGCCTTTTAAT[A/G]ATCCAAAGTTTTTCA | 8453 |
rs115463894 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35116642 | AAAACATTATGTCAA[G/T]TATTTAGTAAATGTT | 8453 |
rs115467743 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35088709 | ATAATCTTCACATTT[A/G]TAGAACACTGAAAGC | 8453 |
rs115493737 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35073491 | TGTGTATACTGCAAG[C/T]CAAGCACTAGTCTAA | 8453 |
rs115583277 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35115928 | AAATAAATGTTGATT[A/C]TTTGAAGAGAGCAAT | 8453 |
rs115599381 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CUL2 | GRCh38.p7 | 10:35094764 | TAGGGAAATAATATT[C/T]GTAAAATAGTTATTA | 8453 |
rs115607676 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35111218 | AAGAATTATGAGATT[A/G]AATGATTCTTTAAGA | 8453 |
rs115707025 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35118035 | ACTGATGAACCTACA[C/T]TGACACATCATAATC | 8453 |
rs115709051 | snp | C/G | 0.00438332 | 0.0466095 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35126961 | GCGTGGGGGAGGGGA[C/G]GACGGGGCGGGAGGA | 8453 |
rs115715059 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074646 | GGCGTGAGCCATCGC[A/T]CCCTAATTTTTGTAT | 8453 |
rs115758721 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | CUL2 | GRCh38.p7 | 10:35017931 | GAGCTGCTTCCTAAA[A/G]CACGAAGTTGTGGTT | 8453 |
rs115774244 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CUL2 | GRCh38.p7 | 10:35088849 | GAAATGTTCCCCCAA[C/T]TCATAAACAGCAATT | 8453 |
rs115774769 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35118690 | TCCCTCTGTGCTCAT[A/T]GCTCATACTTATTCC | 8453 |
rs115778810 | snp | C/G | 0.0178098 | 0.0926698 | upstream-variant-2KB, intron-variant | CUL2 | GRCh38.p7 | 10:35090783 | GAGCTGATGGACACA[C/G]TACCCACCCACTACC | 8453 |
rs115785334 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35062021 | TCAAAACTCAGTCCA[C/T]AAGGTAGTTGTTAAG | 8453 |
rs115816511 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35112751 | ACAGTATTATACAGG[A/G]CATGAGGCAGAATCT | 8453 |
rs115941290 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35043006 | TGGTGTCTGCTGCTT[A/G]GTGTGTGGGAGAAGA | 8453 |
rs115942064 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | CUL2 | GRCh38.p7 | 10:35036544 | CAGTTTCCCAAAGTA[C/G]TTGCATCAATTTATA | 8453 |
rs115947635 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CUL2 | GRCh38.p7 | 10:35030845 | CCAGCCTGGGCAACA[C/T]AGTGAGACCCTATCT | 8453 |
rs116007391 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CUL2 | GRCh38.p7 | 10:35034491 | GAACAGTGACGTCTA[C/T]ACACAGATACTATCT | 8453 |
rs116116145 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080625 | ACTGCACTGAGCTAC[C/T]TTTTTGTATTTGTAG | 8453 |
rs116120961 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35052021 | TTTTCAAGCTTTGCC[G/T]TTCACATTTAGGCCT | 8453 |
rs116146175 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CUL2 | GRCh38.p7 | 10:35095719 | ACATGCCAATACACC[C/T]AGCGAATTTTTTTGT | 8453 |
rs116208262 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35029352 | ATAAGCCACCACGCC[C/T]AGCCCAAATCAATAG | 8453 |
rs116268948 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | CUL2 | GRCh38.p7 | 10:35086927 | GAACAATATTTGCTT[A/G]TATGTCCACAAATAT | 8453 |
rs116346677 | snp | A/C | 0.0618563 | 0.164627 | intron-variant | CUL2 | GRCh38.p7 | 10:35093195 | TGTCCATAAAAACCC[A/C]AACCTCCAACCCAGG | 8453 |
rs116347449 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35063806 | TTCTCAACATCTCCA[A/G]TAATTAGAAACATTA | 8453 |
rs116356479 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CUL2 | GRCh38.p7 | 10:35026343 | CTAACTAATAACTCC[C/T]AGGGATATCAATAAA | 8453 |
rs116493330 | snp | A/G | 0.021333 | 0.101051 | intron-variant | CUL2 | GRCh38.p7 | 10:35034486 | CTCCTGAACAGTGAC[A/G]TCTATACACAGATAC | 8453 |
rs116495270 | snp | A/T | 0.0168055 | 0.0901129 | intron-variant | CUL2 | GRCh38.p7 | 10:35073257 | GATTTTACTCTGCAA[A/T]ATTGAGGGGAAGGTG | 8453 |
rs116532864 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CUL2 | GRCh38.p7 | 10:35123629 | AAGAATGACCAAAAT[C/T]GTTTCAAGGTGTAGA | 8453 |
rs116580183 | snp | A/G | 0.00217706 | 0.032921 | intron-variant | CUL2 | GRCh38.p7 | 10:35029659 | TAAAAAAGTTTTAGA[A/G]AATACATGAATTCAA | 8453 |
rs116662207 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | CUL2 | GRCh38.p7 | 10:35109379 | TTATGTGCCATGCAA[A/T]GTTCTAGGTGCTGGG | 8453 |
rs116719864 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CUL2 | GRCh38.p7 | 10:35041783 | CTTGCGTAATCTGCC[C/T]GCCTCAGCCTCCCAA | 8453 |
rs116806817 | snp | A/G | 0.0414363 | 0.137845 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CREM, CUL2 | GRCh38.p7 | 10:35127047 | GGCTACCGCATCACA[A/G]CTGACGTGAGGACTA | 8453 |
rs116830988 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | CUL2 | GRCh38.p7 | 10:35065110 | TTAACCAATTAACTA[G/T]GTTCTTTTTCTCTAA | 8453 |
rs116840482 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075462 | GTTCTTCATTCCTGT[A/G]CCTTAACGAGATTCC | 8453 |
rs116841099 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35061335 | AAAAATTAGCCAGCC[A/G]TGGTGGCACATGCCT | 8453 |
rs116854281 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35113052 | CAAAAATTGGCTGGC[C/T]GGCATGTGTAATCTC | 8453 |
rs116873365 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35102316 | GTGACTCACACCTGC[A/G]ATCCCAACACTTCGG | 8453 |
rs116884482 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CUL2 | GRCh38.p7 | 10:35021407 | CACACTGCTGTGTAT[A/G]AACATACATTTTTTT | 8453 |
rs116950476 | snp | A/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35125056 | TTTTAAAATCTACAA[A/T]AATCCTAACAGGTAG | 8453 |
rs117049502 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CUL2 | GRCh38.p7 | 10:35105531 | TAACACAGTGGAAAC[C/T]CGTCTCTACTAAAAA | 8453 |
rs117055113 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35123445 | GACAGAAATACTTAG[A/G]ATGAACTATAATGGA | 8453 |
rs117153131 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35086124 | CTGTAGTCCCAGCTC[A/G]GGAAGTGGAGGCTGC | 8453 |
rs117167967 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | CUL2 | GRCh38.p7 | 10:35093300 | GCAATACCTTGGTCT[C/T]GGTGAATTTTGTCTG | 8453 |
rs117172050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35040848 | CATGCAGAGTTCACA[A/G]TGGAGTTTGCGCTCT | 8453 |
rs117197560 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021873 | AGGTGGGGTGGGGTG[A/G]GGTGGGGTGAGGTGG | 8453 |
rs117214550 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075446 | TAAATCTATCAGTCT[C/T]GTTCTTCATTCCTGT | 8453 |
rs117290615 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CUL2 | GRCh38.p7 | 10:35113648 | GGAGAAAAATAGAAA[A/G]ATCAATCAATAGGAA | 8453 |
rs117311475 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CUL2 | GRCh38.p7 | 10:35069141 | CAAACTGCTTGAATT[A/G]TAGGCGTGAGACAAC | 8453 |
rs117314772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35101333 | TTGCTTTCAGCATGG[A/C]GACAACGGGTCTACC | 8453 |
rs117379382 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | CUL2 | GRCh38.p7 | 10:35068173 | CACCTGTAATCTCAG[A/C]ACTTCAGGAGTGCCA | 8453 |
rs117508928 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | CUL2 | GRCh38.p7 | 10:35076571 | TCTCCCACCACTCCC[A/G]TGTACGACCTCATTG | 8453 |
rs117566261 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CUL2 | GRCh38.p7 | 10:35111209 | AGGGAGAACAAGAAT[G/T]ATGAGATTAAATGAT | 8453 |
rs117590640 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | CUL2 | GRCh38.p7 | 10:35038671 | ATTCTAAATGCATTA[A/G]GGAAATTAGCTCTTG | 8453 |
rs117610167 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35096024 | AGTCCGAGGCGGGTG[G/T]ATTGCTCGAGGCCAG | 8453 |
rs117615530 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CUL2 | GRCh38.p7 | 10:35104751 | CTTTTCTGGGGGGGG[A/G]ACAGTCTTGCTCTTG | 8453 |
rs117665807 | snp | A/G | 0.270621 | 0.249148 | intron-variant | CUL2 | GRCh38.p7 | 10:35110445 | TGGTGCACGCCTATA[A/G]TCCCAGATACTCTGG | 8453 |
rs117709492 | snp | A/G | 0.095 | 0.19615 | intron-variant | CUL2 | GRCh38.p7 | 10:35021863 | AGGTGAGGTGAGGTG[A/G]GGTGGGGTGAGGTGG | 8453 |
rs117724027 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | CUL2 | GRCh38.p7 | 10:35064376 | ATAAGGATGCAAATT[C/G]TTTCTCCTCTATGTC | 8453 |
rs117743006 | snp | C/T | 0.124444 | 0.216185 | intron-variant | CUL2 | GRCh38.p7 | 10:35021831 | TGGGGTGAGGTGAGG[C/T]GAGGTGAGGTGAGGT | 8453 |
rs117784954 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35040632 | TCAGGGCAAAGTCAC[A/C]GACTCAGGTCGGGCA | 8453 |
rs117793784 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CUL2 | GRCh38.p7 | 10:35016043 | GATGCCTTAACGCTC[A/G]CAGCTCTATGGAGCG | 8453 |
rs117795549 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CUL2 | GRCh38.p7 | 10:35049212 | CATGGGTAGAGTGGG[A/T]AACCATTTTCCCATA | 8453 |
rs117819306 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CUL2 | GRCh38.p7 | 10:35031865 | TAGTTGGGACTACAG[A/G]CATGCACAACCACAC | 8453 |
rs117819726 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35023219 | TGTAAACAGATACAA[C/T]TTTTATGTGTCAATT | 8453 |
rs117867267 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35053351 | TTCAACATATACCTA[C/T]AATTTTGTGTCCAAA | 8453 |
rs118033151 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35060625 | GGTTGTAAACAATCA[A/G]AAGAAACAGAGCCAT | 8453 |
rs118112561 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074846 | AAGGTGTCCTATCAT[A/G]GGTATTACCTGAGAA | 8453 |
rs118186958 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CUL2 | GRCh38.p7 | 10:35116265 | CAAGAATTCCTTGAA[C/T]CTGGGAGGTGGAGGT | 8453 |
rs137902293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35023316 | TTTCAGTACCTTCGG[A/T]GACTCAAAACAAAAA | 8453 |
rs137987201 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35099077 | GACGTAGTTCCTGGG[C/T]TAAGGAAGGTGGTTG | 8453 |
rs137988188 | snp | C/T | 0.000164919 | 0.00907921 | missense | CUL2 | GRCh38.p7 | 10:35035188 | TTTTCCTGAGTAAGG[C/T]TGCTGGTTGCTCGAA | 8453 |
rs138001467 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CUL2 | GRCh38.p7 | 10:35014401 | TTTTTAGAATAACAA[C/T]TTCTGTATCAGGCTT | 8453 |
rs138015093 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35009779 | CATTCAGATAAAAAC[A/G]CAACTAAAGATGCAT | 8453 |
rs138016870 | snp | C/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35052119 | TTTGTTTGACTCTTC[C/T]CTTTTTCCACCCTAA | 8453 |
rs138124619 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35087262 | GGGGTCTCACCATGT[C/T]GCCCAGACTAACATC | 8453 |
rs138125692 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35094378 | GTAGCTGAGATTACA[A/T]GCACGTGCCACCACG | 8453 |
rs138137356 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35087643 | CATCATCCTCCAGCA[A/G]AAGCCAAAAACCCAG | 8453 |
rs138179289 | in-del | -/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35092890 | TAAAGTGTAGGCATA[-/T]TTTCTATTAATATAC | 8453 |
rs138188209 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021883 | GGGTGAGGTGGGGTG[A/G]GGTGGGGTGAGGTGG | 8453 |
rs138202841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35112777 | AATCTTCAAAAGGTT[A/G]TTGCCTGAGTTGTGA | 8453 |
rs138217452 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35040692 | CTTTTAGGCACCAGG[A/C]TCTGCTTTTGTGGAA | 8453 |
rs138264137 | in-del | -/AAAAAT | 0.0678174 | 0.1712 | intron-variant | CUL2 | GRCh38.p7 | 10:35039857 | GAGACACTGTCTCAA[-/AAAAAT]AAAAATAAGGCCAGG | 8453 |
rs138267894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35124734 | AAAGGCTGTAGGTAT[A/G]ACTCTTGGTAATTGA | 8453 |
rs138313967 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021629 | TTTCATTTATTATTT[A/T]TTATTTTCATTTATT | 8453 |
rs138329813 | snp | A/C/G | 0.00358923 | 0.042236 | intron-variant | CUL2 | GRCh38.p7 | 10:35036215 | TCACACAATTCTTTC[A/C/G]TGTCTGGCTTCTTGT | 8453 |
rs138390878 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35078088 | GCACATCATCTCTAA[C/T]TGAAAGCCGTTACTA | 8453 |
rs138403020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35074705 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGAGGCTC | 8453 |
rs138479453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35021123 | ACCTTAGGGGTTAGA[C/G]CTTCAACAGAAGACT | 8453 |
rs138479757 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CUL2 | GRCh38.p7 | 10:35073629 | TTTTTTTGAGATGGA[A/G]TCTCGCTGTTGTCAG | 8453 |
rs138485947 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35070573 | GGCTTCAGGGCATCC[C/T]AGAGAAATCACCAAT | 8453 |
rs138565996 | in-del | -/A/AA | | | intron-variant | CUL2 | GRCh38.p7 | 10:35077326 | CAAAAACAAACAAAC[-/A/AA]AAACAAAAAAAACAA | 8453 |
rs138571727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35094652 | GAAATGTGATCGAGC[A/G]TGAAGGGTGCCAACC | 8453 |
rs138608007 | snp | C/T | 0.0433465 | 0.140692 | utr-variant-3-prime | CUL2 | GRCh38.p7 | 10:35008892 | CTGAAGTATTATAAG[C/T]GAAATAATTTGTGTG | 8453 |
rs138623644 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CUL2 | GRCh38.p7 | 10:35099492 | CCCAAGATTATACAA[C/T]CAGATTTCTAAAATA | 8453 |
rs138718886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35056769 | TATGCCTTCCAATAC[A/G]GAATCTGCTCCAAAC | 8453 |
rs138757291 | snp | A/G | 0.000297895 | 0.0122008 | synonymous-codon | CUL2 | GRCh38.p7 | 10:35033211 | ACCATTCAAAACAGT[A/G]TTGATAAGCTGAACA | 8453 |
rs138780577 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CUL2 | GRCh38.p7 | 10:35071608 | AGAGACGGGGTTTCA[A/C]TGTGTTAGCCAGGAT | 8453 |
rs138831023 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CUL2 | GRCh38.p7 | 10:35046186 | TCTTGATATCTTGAT[A/G]TCACTGACTAGTTCA | 8453 |
rs138849301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35117327 | ACTGCAGCCTAGTCT[A/G]TCTCACAGGCTCAAT | 8453 |
rs138932904 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35064017 | ACACAGAGGTCAGGA[A/C]CTCCTGGTGGTTATA | 8453 |
rs139006326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CUL2, MIR3611 | GRCh38.p7 | 10:35079105 | TTTTTCATATACATA[C/T]ATACCTATGATAAAG | 8453 |
rs139016436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35024598 | TTAATCCTACTGTAA[A/G]TAAGTGGACTCCATT | 8453 |
rs139037956 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35111944 | AACTCATAGCCTACT[C/G]TCCAGAGATTGGGAG | 8453 |
rs139112799 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35021631 | TCATTTATTATTTTT[A/T]ATTTTCATTTATTTA | 8453 |
rs139115339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35043250 | ACAGAGCAAAGTGCA[C/T]GTATCACAGATAATC | 8453 |
rs139139617 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | CUL2 | GRCh38.p7 | 10:35037200 | ATTGATTTTGTATAT[G/T]GTATCTTGAGGTAGT | 8453 |
rs139152262 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35032803 | CTTTCCTTTAACGTA[C/T]GCAAAAGTTCATGTA | 8453 |
rs139166454 | in-del | -/TTTA | | | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080434 | TTTAGAATTCCTATT[-/TTTA]TTTATTTATTTATTT | 8453 |
rs139186740 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CUL2, MIR3611 | GRCh38.p7 | 10:35080830 | CATATGGTGTGTGCC[A/C]AAATGTATACTGCAG | 8453 |
rs139203791 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CUL2 | GRCh38.p7 | 10:35037800 | GTGAACAGAGATCGC[A/G]CCACTGCATTATAGC | 8453 |
rs139224628 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | CREM, CUL2 | GRCh38.p7 | 10:35126347 | AAGCTTCTTTTGGAG[A/G]AGGACTCAACCAGCT | 8453 |
rs139237399 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35017309 | CTTGCTGAAAGTTGA[C/T]AGCAAAAGAATCTGA | 8453 |
rs139247140 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | CUL2 | GRCh38.p7 | 10:35075977 | ACATAAAAACTGGTA[C/T]ACAAATGTTCACTGT | 8453 |
rs139279111 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CUL2 | GRCh38.p7 | 10:35084233 | AGTGAGCTGAGATCG[C/T]GCCACTGCACTACAG | 8453 |
rs139344542 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35011619 | CAAGACTCTGTCTCA[A/G]CAACAACAACAAAAA | 8453 |
rs139538506 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CUL2 | GRCh38.p7 | 10:35084728 | TCTCATAACATTCCA[A/G]ATCGCTGCTTGTTTT | 8453 |
rs139605464 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CUL2 | GRCh38.p7 | 10:35059344 | TTTAAGACATTGCCA[C/T]AGCCTCCCCAACCTT | 8453 |
rs139611816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35033719 | TCCAGCTTGGGCGAC[A/G]GAGTGAGACTCCGTC | 8453 |
rs139649618 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CUL2 | GRCh38.p7 | 10:35105795 | CTTTACTAAAAGCCA[C/T]GAACCTGGCTCCTGA | 8453 |
rs139656481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CUL2, MIR3611 | GRCh38.p7 | 10:35079633 | CTTTCTTCACAATTT[A/C]TTTTCTTTCATAATT | 8453 |
rs139666469 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CUL2 | GRCh38.p7 | 10:35065543 | AGAATGGCGTGAACC[C/T]GAGAGATGGAGGTTG | 8453 |
rs139669034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CUL2 | GRCh38.p7 | 10:35059590 | CCAAACAACTTGTGT[A/G]ACTTGTCTTACTGCA | 8453 |
rs139764755 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35015874 | TAAAACCAAAAACCT[A/G]GAAAGTCTTTAAAGG | 8453 |
rs139797964 | snp | A/T | | | intron-variant | CUL2 | GRCh38.p7 | 10:35119562 | GTTTTAAAATTAATT[A/T]TATTTATTTATTTAT | 8453 |
rs139809599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35072791 | TAAGCTAAATGTAAT[C/T]GCTCAAAGGAACATT | 8453 |
rs139834376 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35113205 | AAAAAAAAAAAAAAA[A/G]AATTCAGCGGCCAGG | 8453 |
rs139851712 | snp | A/G | 0.000165434 | 0.00909339 | synonymous-codon, intron-variant, utr-variant-5-prime | CUL2 | GRCh38.p7 | 10:35054509 | CGCTTCTGTTAATTT[A/G]TTCTTTTTAATAAAC | 8453 |
rs139853309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CUL2 | GRCh38.p7 | 10:35038125 | ATTGCACTCCAGCCT[A/G]GGCGACGGAGCGAGA | 8453 |
rs139879752 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CUL2 | GRCh38.p7 | 10:35120876 | AATCCAGCCTGGGCC[A/G]TAGAGTAAGAGATCC | 8453 |
rs139900544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CUL2 | GRCh38.p7 | 10:35042344 | ATAACTTCAATTCTT[C/T]TTAAAGACTGTGTGG | 8453 |
rs139926892 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | CREM, CUL2 | GRCh38.p7 | 10:35127744 | GGCAGAGCCGCGACC[G/T]CTCTCGGAAGGCGCA | 8453 |
rs140066280 | snp | A/G | | | intron-variant | CUL2 | GRCh38.p7 | 10:35016419 | AAACAAAAACTGACA[A/G]TGAATTGACCATTCA | 8453 |
rs140068931 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CUL2 | GRCh38.p7 | 10:35101285 | GGCAATAGTGGCTTA[C/T]AATTGTGGGACAGCT | 8453 |
rs140086156 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | CUL2 | GRCh38.p7 | 10:35103290 | TGGGACACAGGCGCC[C/T]GCCACCAGGCCAAGC | 8453 |