SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs26837 | snp | A/G | 0.49889 | 0.0235361 | intron-variant | E4F1 | GRCh38.p7 | 16:2230317 | AGGTCTGGATGGGCA[A/G]GCTCTCATCGGGGAC | 1877 |
rs26838 | snp | C/G | 0.499598 | 0.0141716 | intron-variant | E4F1 | GRCh38.p7 | 16:2231150 | CTAGTGGAGATGGCA[C/G]AGGGTCCTGCCTGCT | 1877 |
rs26839 | snp | A/G | 0.0133536 | 0.0806142 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232255 | CCCCGGGCAGCCCCC[A/G]CCAGCAGGGGCTGGG | 1877 |
rs26840 | snp | C/T | 0.477489 | 0.103676 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235356 | CGACACCATCACCAT[C/T]GCCACCCCCGAGAGC | 1877 |
rs27382 | snp | A/G | 0.49889 | 0.0235361 | intron-variant | E4F1 | GRCh38.p7 | 16:2230276 | GATGTCTCTCTCCCT[A/G]ATGTGCTGTGGGAGG | 1877 |
rs27709 | snp | A/G | 0.435263 | 0.167862 | intron-variant | E4F1 | GRCh38.p7 | 16:2231828 | GCAGGACAGGCGGCT[A/G]TCTCTTCACCCAAGG | 1877 |
rs30985 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | E4F1 | GRCh38.p7 | 16:2226663 | AGTGTCAGGGACAGT[A/G]CCTGTTTACACAAAG | 1877 |
rs30986 | snp | A/G | 0.432797 | 0.170544 | intron-variant | E4F1 | GRCh38.p7 | 16:2225866 | cctcgggatccgccc[A/G]tctcagcctcccaaa | 1877 |
rs30987 | snp | A/G | 0.499908 | 0.00678851 | intron-variant | E4F1 | GRCh38.p7 | 16:2225685 | cgggagttcaagacc[A/G]gcctggccaacatgg | 1877 |
rs30988 | snp | A/G | 0.499759 | 0.0109798 | intron-variant | E4F1 | GRCh38.p7 | 16:2224299 | ACCCAGGATCAAAGA[A/G]CTAGAAAGCGGCAAG | 1877 |
rs30989 | snp | C/G | 0.251014 | 0.249998 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221605 | ggagttcaagaccaa[C/G]caggccaacatggca | 1877 |
rs313910 | snp | G/T | 0.175576 | 0.238665 | intron-variant | E4F1 | GRCh38.p7 | 16:2229370 | ACCCTGGCCCGGGGG[G/T]GAAGGGATTGGACTG | 1877 |
rs1056834 | snp | C/G | 0 | 0 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235260 | GCAGATCGTGCACCA[C/G]GCTAGCGCCGGCCAC | 1877 |
rs1056869 | snp | C/T | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235620 | ACAGGGCAGAGGACT[C/T]TGAGCGCCCCACCCA | 1877 |
rs1612140 | snp | A/G | 0.164546 | 0.234942 | intron-variant | E4F1 | GRCh38.p7 | 16:2225767 | AGACTGGGAGGAGCC[A/G]GGCACGGTGGCGCAC | 1877 |
rs1640780 | snp | C/T | 0.164219 | 0.234823 | intron-variant | E4F1 | GRCh38.p7 | 16:2225699 | CTGGTCTTGAACTCC[C/T]GACCTCAGGTGATCT | 1877 |
rs1804823 | snp | A/C/T | 1.84862e-05 | 0.00304019 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235483 | GTGACCATGGTGTCA[A/C/T]CAGAGGACATCGAGA | 1877 |
rs2241070 | snp | A/G | 0.0966694 | 0.197458 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228508 | CCCTGCCACCACAGC[A/G]TTGCTGGGCCAGGAG | 1877 |
rs2241071 | snp | A/G | 0.373397 | 0.217424 | intron-variant | E4F1 | GRCh38.p7 | 16:2229369 | GACCCTGGCCCGGGG[A/G]TGAAGGGATTGGACT | 1877 |
rs2302584 | snp | A/C/T | 0.00207496 | 0.032143 | synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234763 | CACGGCACGCTGAAC[A/C/T]GGCACCTGCGCACCA | 1877 |
rs3096278 | snp | C/T | 0.165527 | 0.235296 | intron-variant | E4F1 | GRCh38.p7 | 16:2226088 | TTTTTTCTTTCAAGG[C/T]GGAGTCTCGCTTTGT | 1877 |
rs3114131 | snp | C/G | 0.202343 | 0.245416 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234514 | TCTCCCCTCCCGCCT[C/G]TGGCCCAAGGGAGGG | 1877 |
rs8056361 | snp | A/G | 0.175897 | 0.238765 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222891 | gcctggcgtggtggc[A/G]gacacctgtagtccc | 1877 |
rs8057731 | snp | A/G | 0.0479149 | 0.147179 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222654 | tggtttgaggctagg[A/G]gtttgagaccagcct | 1877 |
rs9928419 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225526 | ttgcccaggctggag[C/T]gcaatggtgcgatct | 1877 |
rs11640867 | snp | C/T | 0.000177984 | 0.00943188 | intron-variant | E4F1 | GRCh38.p7 | 16:2233668 | TGCCAGCACCACCTG[C/T]GGGCTCCTCCCAGGG | 1877 |
rs11641096 | snp | A/G | 0.495927 | 0.0449436 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221670 | aagtgctgggattac[A/G]ggagtgagccactgt | 1877 |
rs11648028 | snp | C/T | 0.5 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2231341 | CCCCATCAGAGGCCT[C/T]TGTCCTTTGGAAGAT | 1877 |
rs11648224 | snp | C/G | 0 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2226492 | TGCAGGCGAGTCATA[C/G]CTGTGGTTTGGCCCT | 1877 |
rs12935005 | snp | C/T | 0 | 0 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223849 | CCCGGATGGCCCGAG[C/T]TGCGGGCTCGACCGA | 1877 |
rs34008168 | in-del | -/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227844 | TTTTTTTTTTTTTTT[-/T]GGTAGAGATGGGTCT | 1877 |
rs34062468 | in-del | -/C | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228672 | GGTGTGGGAGGGTCC[-/C]GGGTGTGTGAGCCTG | 1877 |
rs34166917 | in-del | -/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231555 | AACCTGAACTGTGTT[-/T]ACAACCTAGCTTTGC | 1877 |
rs34243234 | in-del | -/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225490 | CTTTTTTTTTTTTTT[-/T]GAGACGGCGTTTCTC | 1877 |
rs34274744 | in-del | -/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222930 | GGAGGCTGAGGCAGG[-/T]AGAATGGCGTGAACC | 1877 |
rs34615954 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230274 | AAGATGTCTCTCTCC[C/T]TAATGTGCTGTGGGA | 1877 |
rs35080768 | in-del | -/T | 0 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2227844 | TTTTTTTTTTTTTTT[-/T]GGTAGAGATGGGTCT | 1877 |
rs35320604 | in-del | -/G | | | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235867 | CCGCCCCACCCAGGG[-/G]CTTCTGCCAGCCCTG | 1877 |
rs35337547 | snp | C/T | 0.0168055 | 0.0901129 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228385 | GCGGCCGCATCTGTG[C/T]ACATCGTCCTCATCT | 1877 |
rs35339015 | in-del | -/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2233814 | GGGTGGGGCCCATGG[-/G]TTGTGTTCTTGGTAC | 1877 |
rs35368180 | in-del | -/GA | 0.473451 | 0.112115 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221663 | CTCCCAAAGTGCTGG[-/GA]GATTACGGGAGTGAG | 1877 |
rs35436732 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | E4F1 | GRCh38.p7 | 16:2231323 | CATGTTCCCCCAGGT[C/T]CTCCCCATCAGAGGC | 1877 |
rs35483132 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | E4F1 | GRCh38.p7 | 16:2231011 | GCCCCTCTTGGCACC[C/T]CTGCCACTCTGGCAC | 1877 |
rs35508264 | snp | C/G | 0.00528437 | 0.0511299 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233474 | GGTTCTCACGGCTGC[C/G]CTCGCTGGAGCAGGG | 1877 |
rs35589455 | in-del | -/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231669 | CGTTCACTCTCCCAG[-/G]CCAAGCCTGCCTTGG | 1877 |
rs35739041 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233509 | CACCAGGCCATGCAG[-/C]AACTCCGGCATCGTC | 1877 |
rs56828353 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | E4F1 | GRCh38.p7 | 16:2229845 | GCAGGAGGAGGAAGC[A/G]TTGGGCACTGGGCCT | 1877 |
rs57106550 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225691 | TGGCCAGGCTGGTCT[C/T]GAACTCCCGACCTCA | 1877 |
rs57862391 | snp | A/G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223517 | CTCCGGTTCTGCCCC[A/G/T]CCCTCCTCTTGCCGT | 1877 |
rs58584758 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | E4F1 | GRCh38.p7 | 16:2234058 | CGGGGTGCTTCTGGG[C/T]GTCCAGGGTGGGTCC | 1877 |
rs58700030 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225720 | CAGGTGATCTGCCCG[C/T]CTCAGCCTCCCAAAG | 1877 |
rs59007121 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225714 | CGACCTCAGGTGATC[C/T]GCCCGCCTCAGCCTC | 1877 |
rs59101267 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225865 | CTTTGGGAGGCTGAG[A/G]CGGGCGGATCCCGAG | 1877 |
rs59563983 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | E4F1 | GRCh38.p7 | 16:2229747 | GATGGGGCCCCTGCT[G/T]CCTGTATGCTCGTCT | 1877 |
rs59620278 | snp | A/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225661 | ATTTTTAGTAGAGAC[A/T]GGATTTCTCCATGTT | 1877 |
rs59759998 | snp | C/T | 0.0185399 | 0.0944786 | intron-variant | E4F1 | GRCh38.p7 | 16:2233843 | ACTGCCAGGGCACAG[C/T]CTGCCCCGGGTGCTG | 1877 |
rs59784157 | snp | A/G/T | 0.0112773 | 0.0742411 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233444 | CCCCTGCAGCCCCCC[A/G/T]TCTCCCAGGAGCTCC | 1877 |
rs59845216 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | E4F1 | GRCh38.p7 | 16:2233327 | AGGGCCAGTGGGAGC[G/T]CCATGGGGGTCTGAG | 1877 |
rs60013960 | in-del | -/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229369 | ACCCTGGCCCGGGGG[-/G]TGAAGGGATTGGACT | 1877 |
rs60612119 | snp | G/T | 0.029116 | 0.117091 | intron-variant | E4F1 | GRCh38.p7 | 16:2231788 | CCTATGTTGGTGGGA[G/T]CAGTGGCAGGAGCAG | 1877 |
rs62040662 | snp | G/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228798 | TTCTTGGAGCTGGAG[G/T]GTCTCCTTTGGCTCT | 1877 |
rs71394733 | in-del | -/A | 0.5 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2227024 | GCTCAAACTCCCGCA[-/A]GTTTTTGTTTGTTTG | 1877 |
rs72766666 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222687 | TCTAAACAGCAAGAC[C/T]CTGTCTCTATTTAAA | 1877 |
rs73500107 | snp | G/T | 0.029116 | 0.117091 | intron-variant | E4F1 | GRCh38.p7 | 16:2226796 | GGTGCTTGGCACACA[G/T]TGAGGGGGTGGTCTC | 1877 |
rs74367875 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | E4F1 | GRCh38.p7 | 16:2224662 | AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTAGTGG | 1877 |
rs74695663 | snp | A/G | 0.0209421 | 0.100162 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235846 | CTCCTAGACTCACGT[A/G]CCTGGCCGCCCCACC | 1877 |
rs75636456 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | E4F1 | GRCh38.p7 | 16:2231923 | GGTCTCCCTGTGGAC[A/G]CATTTAGGGGCCCTG | 1877 |
rs75956074 | snp | G/T | 0.5 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2225489 | TCTTTTTTTTTTTTT[G/T]TGAGACGGCGTTTCT | 1877 |
rs76885746 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | E4F1 | GRCh38.p7 | 16:2224387 | GCCAGTAATGTAACA[A/G]GCCCTTATCCTGCTT | 1877 |
rs77536843 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | E4F1 | GRCh38.p7 | 16:2230326 | TGGGCAGGCTCTCAT[C/T]GGGGACAGATGCTTG | 1877 |
rs78398423 | snp | C/T | 0.0325976 | 0.123435 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235852 | GACTCACGTGCCTGG[C/T]CGCCCCACCCAGGGG | 1877 |
rs78729709 | snp | G/T | 0 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2225491 | TTTTTTTTTTTTTTT[G/T]AGACGGCGTTTCTCT | 1877 |
rs79253733 | snp | C/G | 0.5 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2224994 | AAGGTGGGTGGATCA[C/G]CTGAGGTCAGGAGTT | 1877 |
rs79982505 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | E4F1 | GRCh38.p7 | 16:2230456 | AGACGCGAGGGAAGG[A/C]GCTGTCTAGGGACCT | 1877 |
rs80084951 | snp | A/C | 0.5 | 0 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233553 | CTGGGGAGGAGGGTG[A/C]CCTGGAGCCAGCTCC | 1877 |
rs111361324 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224956 | AGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG | 1877 |
rs111514458 | snp | A/G | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223501 | CCTGTCCGTCAATCC[A/G]CTCCGGTTCTGCCCC | 1877 |
rs111767084 | in-del | -/G | 0.17461 | 0.238362 | intron-variant | E4F1 | GRCh38.p7 | 16:2229364 | CGCTGACCCTGGCCC[-/G]GGGGGTGAAGGGATT | 1877 |
rs111797145 | snp | A/C | 0.5 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2231330 | CCCCAGGTCCTCCCC[A/C]TCAGAGGCCTCTGTC | 1877 |
rs112325888 | in-del | -/T | 0 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2225806 | AAAAAAAAAAAAAAA[-/T]AAAAAAAGGCTGGGC | 1877 |
rs112564078 | snp | C/T | 0.5 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2229002 | CCGCACACGCCGCAG[C/T]GGGCGCTTGTCATCC | 1877 |
rs112862402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2231823 | AGCGAGCAGGACAGG[C/T]GGCTGTCTCTTCACC | 1877 |
rs112919582 | snp | A/T | 0.128632 | 0.218563 | intron-variant | E4F1 | GRCh38.p7 | 16:2225810 | AAAAAAAAAAAAAAA[A/T]AAAGGCTGGGCGCAA | 1877 |
rs112938340 | snp | A/C/G/T | 0.000302858 | 0.0123026 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234790 | ACCAAAGGTCTGGGC[A/C/G/T]GGTGGAGGTGGGAGG | 1877 |
rs112969870 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222816 | TCACGAGGTCAGGAG[A/G]TCGAGACCATCCTGG | 1877 |
rs113062677 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | E4F1 | GRCh38.p7 | 16:2225144 | CTTGAGCCCAGGAGA[C/T]GGAGGTCGCAGTAAG | 1877 |
rs113244233 | snp | A/G | 0.5 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2225497 | TTTTTTTTTGAGACG[A/G]CGTTTCTCTCTTGTT | 1877 |
rs113268992 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221577 | TTTTGTATTTTTAGT[A/G]AAGACGTAATTTTGC | 1877 |
rs113270919 | snp | C/G/T | 6.98731e-05 | 0.00591036 | missense, synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234184 | AGGGCCGAGGCCGTT[C/G/T]GCCTGCGCGCAGTGT | 1877 |
rs113465416 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | E4F1 | GRCh38.p7 | 16:2226397 | GAGTAGGGTGGGAAG[A/G]GGAAGAGGGTGGTGG | 1877 |
rs113710566 | snp | C/T | 0.5 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2232698 | TGCCTGCCTTCGCCT[C/T]GTCACCTTGTCGCCA | 1877 |
rs113976652 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229560 | CCCTGTTTTCTTCCC[A/C/T]CTTTGGCAGGTGGTG | 1877 |
rs114147924 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235854 | CTCACGTGCCTGGCC[A/G]CCCCACCCAGGGGCT | 1877 |
rs114578394 | snp | A/G | 0.0524604 | 0.153226 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235918 | GGGTGTCATTGGCAT[A/G]TTGACCAACAGCCTC | 1877 |
rs115208946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230188 | GTGGGAGTGGTGATT[A/G]CTACACTGGTCCTCA | 1877 |
rs115624510 | snp | A/G | 0.000720898 | 0.0189718 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235460 | CAAGTGGCACTGAAC[A/G]GGCCACTGTGACCAT | 1877 |
rs116064450 | snp | G/T | 0.00874735 | 0.0655527 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223198 | CCCTGGTTGGAGCTG[G/T]GGCGGCTTCCCAGCA | 1877 |
rs117057799 | snp | C/T | 0.000374366 | 0.0136764 | intron-variant | E4F1 | GRCh38.p7 | 16:2232371 | TTCAAGACGGTGAGC[C/T]GGCGTGCGGGGAGCC | 1877 |
rs117454577 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | E4F1 | GRCh38.p7 | 16:2231966 | GCAGCCTGACAGAGT[C/T]GGGAGGTGTCTCTCC | 1877 |
rs137969975 | snp | A/G | 0.000466656 | 0.0152679 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234191 | AGGCCGTTCGCCTGC[A/G]CGCAGTGTGGCAAGG | 1877 |
rs138184443 | snp | A/G | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232186 | GTGGTGGGCACATCA[A/G]AGAGGTCATCGTGGC | 1877 |
rs138215085 | snp | A/G | 0.000153988 | 0.00877327 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233494 | CCGTGAGAACCTGCT[A/G]CACCAGGCCATGCAG | 1877 |
rs138258884 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | E4F1 | GRCh38.p7 | 16:2226157 | GTTAATGATTGGGTT[G/T]AGGGTGGTCTTGTCT | 1877 |
rs138375156 | snp | A/G | 0.00999845 | 0.0699947 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235436 | CTGTGCTTGCCGCCC[A/G]GGCAGGGACAAGTGG | 1877 |
rs138466132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2229057 | CTCAGAAAGTGGTCA[A/G]TGGCCTCTGGCCACC | 1877 |
rs138635935 | snp | A/G | 0.000142369 | 0.00843589 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234947 | GGAAGACCCGCACAC[A/G]GTGTTGGTGGAGTTC | 1877 |
rs138679168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229300 | TCCCTCCCTGCAGGC[A/G]CCCTGTGCTCCAGGT | 1877 |
rs138985848 | snp | A/C/G | 6.97075e-05 | 0.00590335 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235285 | GGCCACCAGATCATC[A/C/G]TGCAGAACGTCACCA | 1877 |
rs139395951 | snp | A/G | 0.000154995 | 0.00880189 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235404 | CATGACGCTGGCCTC[A/G]GCCATCAGCGAGGGC | 1877 |
rs139411986 | snp | C/T | 0.000100572 | 0.00709053 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228418 | CCAGGCAGAGTTCAC[C/T]GCCTTGGAGGATTTT | 1877 |
rs139438270 | snp | A/G | 0.00139537 | 0.0263769 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232805 | GAGCTTCCGGGAGTC[A/G]GGTGCACTGACCCGG | 1877 |
rs139464530 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222289 | TTGGGAGGCCGAGGC[A/G]GGCAGATCGTGAGGT | 1877 |
rs139624156 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236221 | TGGCTGACCGTCTAC[C/T]TCCCTCCTAGGGGGC | 1877 |
rs139791282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2232030 | CCTTGGCTGTTGCTC[A/G]GACCTGTGTGTTGAG | 1877 |
rs140042589 | in-del | -/A | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231274 | CCTGCCGCTTCGCGG[-/A]AAAAGTTCGCGTCTC | 1877 |
rs140166330 | snp | C/T | 0.000150312 | 0.00866795 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232775 | GCGCCCCTACAAGTG[C/T]TCCAAGTGTGGAAAG | 1877 |
rs140184126 | snp | C/T | 1.67405e-05 | 0.00289309 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234312 | AGACCATTGCCCATG[C/T]GCGTGGCCACCGGCG | 1877 |
rs140445968 | snp | A/G | 1.66032e-05 | 0.0028812 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232858 | GCACAGAGAAAATCC[A/G]CTTCAGTGTGAGCAA | 1877 |
rs140454954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227363 | TACAGGCATGCGCCA[C/G]CAAGCCTGGCTAATA | 1877 |
rs140552076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230126 | TCTCTAGCTGGGCTC[A/G]GACTTGCTGCTGGCC | 1877 |
rs140659034 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | E4F1 | GRCh38.p7 | 16:2228771 | GTGCTGTTGGGGGCC[A/G]GGATCTCTTCTTTCT | 1877 |
rs140819575 | snp | A/G | 0.000400532 | 0.0141459 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235479 | CACTGTGACCATGGT[A/G]TCATCAGAGGACATC | 1877 |
rs140972388 | snp | A/G | 0.00224544 | 0.0334317 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234725 | CGTTCAAGTGCTACA[A/G]GTGCGGCCGTGGCTT | 1877 |
rs141058515 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2225608 | CCTCCTGAGTAGCTG[C/G]GATTACGGCACGCGG | 1877 |
rs141119759 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | E4F1 | GRCh38.p7 | 16:2224769 | GCCTGGGCGGCAGAG[C/T]CGGACTCCGTCTCAA | 1877 |
rs141145527 | snp | A/G | 0.00159095 | 0.0281592 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233534 | ATCGTCCTTGAGCGC[A/G]CTGCTGGGGAGGAGG | 1877 |
rs141164372 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | E4F1 | GRCh38.p7 | 16:2227662 | CAAGCATGAGCCACC[A/G]CCCTAATTTTGTATT | 1877 |
rs141255210 | snp | A/C | 0.00213719 | 0.0326195 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229613 | AGCCCATCACTGTGG[A/C]CCACATCGTGGTGGA | 1877 |
rs142130361 | snp | C/T | 0.00013938 | 0.00834689 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235313 | CCATGGACGAGGAGA[C/T]GGCGCTGGGCCCAGA | 1877 |
rs142165926 | snp | C/T | 0.000292497 | 0.0120898 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234931 | CCACCACCGTCCTCA[C/T]GGAAGACCCGCACAC | 1877 |
rs142204952 | in-del | -/A | 0.0189856 | 0.0955633 | intron-variant | E4F1 | GRCh38.p7 | 16:2230432 | CAGGGGCGAGTGGCT[-/A]AGGTGTGCAGACGCG | 1877 |
rs142229326 | snp | C/T | 0.000567647 | 0.0168375 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233515 | GGCCATGCAGAACTC[C/T]GGCATCGTCCTTGAG | 1877 |
rs142292722 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | E4F1 | GRCh38.p7 | 16:2224602 | AGACCATCCTGGCCA[A/G]CATGGTGAAACCCGT | 1877 |
rs142312413 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | E4F1 | GRCh38.p7 | 16:2226889 | TCCCAAGTCAGTGAG[A/C]AGAGTGGTTGTGGGT | 1877 |
rs142410368 | snp | A/G | 0.000174828 | 0.00934792 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235267 | GTGCACCAGGCTAGC[A/G]CCGGCCACCAGATCA | 1877 |
rs142656555 | snp | A/C/T | 0.000269405 | 0.0116033 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232243 | AGATGGCCGAGGCCC[A/C/T]GGGCAGCCCCCGCCA | 1877 |
rs142774941 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234373 | TCCCAAGTGTGGCAA[A/G]CGCTACAAGACTAAG | 1877 |
rs142977286 | snp | C/T | 5.04274e-05 | 0.00502107 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234269 | CGTGAGCGCCGCTTC[C/T]GCTGTGGCGACTGCG | 1877 |
rs143029764 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | E4F1 | GRCh38.p7 | 16:2229187 | CCTCTGGCCCACACC[C/T]CCAGGGCCCTCTCCT | 1877 |
rs143057820 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | E4F1 | GRCh38.p7 | 16:2228672 | CGGTGTGGGAGGGTC[C/T]GGGTGTGTGAGCCTG | 1877 |
rs143134295 | snp | A/T | 0.000215726 | 0.0103835 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229587 | GGTGCCGGCAGCACC[A/T]GGCCCAGAGGAGCCC | 1877 |
rs143221732 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233039 | GCTGCCGGCTTGGGG[-/C]ACAGCCACATCATCG | 1877 |
rs143429694 | snp | A/C/T | 0.00025983 | 0.0113952 | synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235088 | CTGCCCAGGCCACTG[A/C/T]GGACGATGCGGAGAC | 1877 |
rs143442513 | snp | C/G/T | 0.000596587 | 0.0172611 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232197 | ATCAAAGAGGTCATC[C/G/T]TGGCTGCTGAGGCGG | 1877 |
rs143899809 | snp | C/T | 0.000755968 | 0.0194271 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235573 | ACGGTCATCGTCTAG[C/T]ATGAGGTCTGCGGGG | 1877 |
rs143952001 | snp | C/T | 3.3493e-05 | 0.00409211 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234323 | CATGTGCGTGGCCAC[C/T]GGCGCGTCCACTCAG | 1877 |
rs144301153 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226592 | TGCCGAGGGACTGAA[A/G]GTGAATGGTCAGAGC | 1877 |
rs144345375 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222626 | AGCACTTTGGGAGGC[C/T]GAAATGGGAAAATGG | 1877 |
rs144383218 | snp | C/T | 0.000133638 | 0.00817318 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232495 | GTCACTCACAGCAGC[C/T]GCAAGGACCACGAGT | 1877 |
rs144477614 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2224616 | AACATGGTGAAACCC[A/G]TCTCTACTAAAAATA | 1877 |
rs144494405 | snp | C/T | 1.98403e-05 | 0.00314956 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232465 | CCACAGGGCAGCATC[C/T]TCAAGGCCCACATGG | 1877 |
rs144562619 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | E4F1 | GRCh38.p7 | 16:2227572 | AGAGACGGGGTTTCA[C/T]GGTGTTAGCCAGGAT | 1877 |
rs144673455 | snp | C/G/T | 0.000733695 | 0.0191394 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235269 | GCACCAGGCTAGCGC[C/G/T]GGCCACCAGATCATC | 1877 |
rs144836270 | snp | C/T | 3.34924e-05 | 0.00409208 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234326 | GTGCGTGGCCACCGG[C/T]GCGTCCACTCAGACG | 1877 |
rs144878577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228262 | GAAGTAGCTCTGCTT[C/T]TGATGGCCTCCTGGG | 1877 |
rs144964049 | snp | G/T | 6.96173e-05 | 0.00589947 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228511 | TGCCACCACAGCGTT[G/T]CTGGGCCAGGAGGTG | 1877 |
rs144987188 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223485 | CAGGCCCGGCTCCCC[A/G]CCTGTCCGTCAATCC | 1877 |
rs145239569 | snp | C/T | 1.66225e-05 | 0.00288287 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232886 | CAAGGACGTGGTTGT[C/T]AGCAAAGAGGACGCA | 1877 |
rs145769654 | snp | A/G | 0.00779656 | 0.0619475 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233522 | CAGAACTCCGGCATC[A/G]TCCTTGAGCGCGCTG | 1877 |
rs145913612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228877 | CACACAGTCCCTAGG[A/G]ACTTCACACGTGAAG | 1877 |
rs146111343 | snp | C/T | 0.000268285 | 0.0115789 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234283 | CCGCTGTGGCGACTG[C/T]GGGAAGCTCTACAAG | 1877 |
rs146160872 | snp | A/G | 9.37321e-05 | 0.00684524 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232509 | CCGCAAGGACCACGA[A/G]TGCAAGCTCTGTGGG | 1877 |
rs146307162 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221934 | CTGTTTCAAAAAAAA[A/G]TCTGGCCAGGCTCGG | 1877 |
rs146393111 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | E4F1 | GRCh38.p7 | 16:2225966 | GCCGTGGTGGCAGGC[A/G]CCTGTAGTCACAGCT | 1877 |
rs146632512 | snp | C/G | 0.00288965 | 0.0379008 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228493 | GGCCCTGCCTGCCAC[C/G]CCTGCCACCACAGCG | 1877 |
rs146690492 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | E4F1 | GRCh38.p7 | 16:2233344 | CATGGGGGTCTGAGG[A/G]TTTGCACAAGGCTCC | 1877 |
rs146861908 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | E4F1 | GRCh38.p7 | 16:2228702 | GTGGTGCTCTGGGGC[A/G]TCCTGGAGGGCCTGC | 1877 |
rs146976541 | snp | C/T | 0.000608947 | 0.0174385 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233489 | GGCAGCCGTGAGAAC[C/T]TGCTGCACCAGGCCA | 1877 |
rs147019267 | snp | A/G | 0.000331686 | 0.0128737 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229624 | GTGGCCCACATCGTG[A/G]TGGAGGCGGCCTCTC | 1877 |
rs147071848 | snp | C/T | 0.0126768 | 0.0785984 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234938 | CGTCCTCACGGAAGA[C/T]CCGCACACAGTGTTG | 1877 |
rs147409290 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235687 | GGAGGCGCCCCAAGA[C/T]GGACAGTGTACATAA | 1877 |
rs147438958 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | E4F1 | GRCh38.p7 | 16:2231402 | CGGGCAGGAGAGGCT[C/G]TTAATTGTTTCTGAG | 1877 |
rs147602177 | snp | C/T | 0.000155988 | 0.00883004 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234729 | CAAGTGCTACAAGTG[C/T]GGCCGTGGCTTCGCC | 1877 |
rs147847239 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | E4F1 | GRCh38.p7 | 16:2227605 | TCTCAATCTCCTGAC[A/C]TCATGATCCGCCCGC | 1877 |
rs148003042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225242 | TTGTGTGTCATGTGC[C/T]GAGAGCAGTGTTGGG | 1877 |
rs148011220 | snp | C/G/T | 1.75213e-05 | 0.00295978 | utr-variant-3-prime, missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235251 | GGTGGTGCAGCAGAT[C/G/T]GTGCACCAGGCTAGC | 1877 |
rs148206065 | snp | C/T | 0.000244141 | 0.0110458 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233531 | GGCATCGTCCTTGAG[C/T]GCGCTGCTGGGGAGG | 1877 |
rs148259822 | snp | A/G | 0.00121002 | 0.0245672 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229612 | GAGCCCATCACTGTG[A/G]CCCACATCGTGGTGG | 1877 |
rs148311962 | snp | C/T | 0.000351726 | 0.0132567 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234340 | GCGCGTCCACTCAGA[C/T]GAGCGGCCCTACCCT | 1877 |
rs148570427 | snp | G/T | 1.95448e-05 | 0.00312602 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232480 | CTCAAGGCCCACATG[G/T]TCACTCACAGCAGCC | 1877 |
rs148750102 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | E4F1 | GRCh38.p7 | 16:2226737 | GGGAATAGTTCTCTC[C/T]ATTTCCACAGGGTGC | 1877 |
rs148830665 | snp | A/C/G | 0.000220264 | 0.0104922 | intron-variant, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234999 | CAGGAGTATATCATC[A/C/G]AGGTGGGTGTGGGGC | 1877 |
rs148945075 | snp | C/G | 1.66128e-05 | 0.00288204 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229579 | TGGCAGGTGGTGCCG[C/G]CAGCACCAGGCCCAG | 1877 |
rs149258624 | snp | C/G/T | 8.45753e-05 | 0.00650245 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232274 | GCAGGGGCTGGGGCT[C/G/T]GCAGGGGAGGGTGAG | 1877 |
rs149377192 | snp | A/G | 0.000647878 | 0.0179866 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229575 | CCTTTGGCAGGTGGT[A/G]CCGGCAGCACCAGGC | 1877 |
rs149872852 | snp | A/C/G | 0.00478364 | 0.0487146 | intron-variant | E4F1 | GRCh38.p7 | 16:2228224 | CCTTGTTTTGGGCCC[A/C/G]AGTGTGTTCTCAGCA | 1877 |
rs149925798 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223299 | TCCGCTCGCCCCTCG[C/T]GTTCTCTGGCTCTCA | 1877 |
rs150020970 | snp | C/T | 4.98326e-05 | 0.00499138 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232877 | CAGTGTGAGCAAGGA[C/T]GTGGTTGTCAGCAAA | 1877 |
rs150196644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229191 | TGGCCCACACCTCCA[A/G]GGCCCTCTCCTCACA | 1877 |
rs150565666 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | E4F1 | GRCh38.p7 | 16:2226964 | TCTCCTGGGCCCCAG[C/T]CCATTTTACAGATGA | 1877 |
rs150638846 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222850 | TCACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 1877 |
rs150753552 | snp | A/G/T | 0.000669371 | 0.0182833 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233897 | CAGGTGGCCAGCGAG[A/G/T]CCTCAGCGGTGCCCA | 1877 |
rs150933849 | snp | A/G | 0.0191139 | 0.0958728 | intron-variant | E4F1 | GRCh38.p7 | 16:2232600 | GCCGCACCTCGGGCT[A/G]GAGCCCGGTAGCACC | 1877 |
rs151069167 | snp | C/T | 0.000510896 | 0.0159746 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234630 | GGAGGAGAAGCCGCA[C/T]GTGTGCCAGTTCTGC | 1877 |
rs180969770 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | E4F1 | GRCh38.p7 | 16:2227060 | TTTTTGTTTCTTTTA[A/G]GGCAGGGTCTTGCCC | 1877 |
rs181261942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227253 | CTCTCTCTGTTGCCC[C/T]GGCTGGAGTGCAATG | 1877 |
rs181388128 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2231625 | AAGCCCAGCTTCCTC[A/G/T]CCTCAGGCTGTCCCG | 1877 |
rs182042349 | snp | C/G/T | 0.000949604 | 0.0217695 | intron-variant | E4F1 | GRCh38.p7 | 16:2232921 | CAGGTCAGCATGGTG[C/G/T]GGGCAGCTGCCTGGT | 1877 |
rs182105825 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235979 | GCTGCGCTGCCTGAG[A/G]CCTGTGGGTGGGTGG | 1877 |
rs182234785 | snp | A/G | 0.00154944 | 0.0277907 | intron-variant | E4F1 | GRCh38.p7 | 16:2229683 | CCTTGTTGGTAAGCC[A/G]ACTTCCATGAATCGC | 1877 |
rs182468779 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230297 | CTGTGGGAGGGGCTG[C/T]TGCGAGGTCTGGATG | 1877 |
rs183058723 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221825 | TAGCTAGTGATGGGC[A/G]CCTGTAGTCCCAGCT | 1877 |
rs183233336 | snp | C/T | 0.000104546 | 0.00722925 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235318 | GACGAGGAGACGGCG[C/T]TGGGCCCAGAGGCGG | 1877 |
rs183960132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2230893 | TCCTTAGGTTCTGGC[A/G]GGGTCTCTGGGCTGG | 1877 |
rs184018937 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | E4F1 | GRCh38.p7 | 16:2227689 | TATTTTTAGTAGAGA[C/T]GGGATTTCACCATAT | 1877 |
rs184022099 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222749 | AAAAAGTGGCTGGGC[A/G]CGGTGGCTCACGCCT | 1877 |
rs184349576 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | E4F1 | GRCh38.p7 | 16:2224771 | CTGGGCGGCAGAGCC[A/G]GACTCCGTCTCAAAA | 1877 |
rs185025443 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | E4F1 | GRCh38.p7 | 16:2230631 | GCTGCAGCAGGAAGA[C/G]GGGGTGGAGGAGCCG | 1877 |
rs185139637 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | E4F1 | GRCh38.p7 | 16:2227063 | TTGTTTCTTTTAAGG[C/T]AGGGTCTTGCCCTGT | 1877 |
rs185238292 | snp | A/C/T | 0.000379827 | 0.0137759 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235494 | GTCATCAGAGGACAT[A/C/T]GAGATCCTGGAGCAT | 1877 |
rs185596737 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | E4F1 | GRCh38.p7 | 16:2225578 | TCCCGGGTTCAAGCT[A/G]TTCTCCTGACTCGGC | 1877 |
rs185622017 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | E4F1 | GRCh38.p7 | 16:2231743 | AGCCCATCTCCTCCG[A/G]TGGAAGAGTGGCCCC | 1877 |
rs186246061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227472 | TGCCTGCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 1877 |
rs186472853 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | E4F1 | GRCh38.p7 | 16:2229945 | GTCAGCTTTCCCGGG[A/T]GGTCTCTGCCGTGTC | 1877 |
rs186588193 | snp | A/G | 0.000970981 | 0.0220124 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233163 | GAGCTGTCCCTGGGC[A/G]TGAAAGCCCTGGCCC | 1877 |
rs187072710 | snp | A/G | 0.0259142 | 0.11084 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223803 | GAGGGTGCGGCCGGG[A/G]TGCGGGCAGTTCATC | 1877 |
rs187350610 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222228 | CTCCATCTCAAAAAA[C/T]AAAAACAGGCCGGGC | 1877 |
rs187574364 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | E4F1 | GRCh38.p7 | 16:2227856 | TTTTGGTAGAGATGG[G/T]TCTTGCTATGTTGAC | 1877 |
rs187721152 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223052 | AAAAATTAAAAGTAT[A/G]TAAAAGAATAAAACA | 1877 |
rs188243983 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231264 | TCCAGGCCCTCCTGC[C/T]GCTTCGCGGAAAAAG | 1877 |
rs188315191 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236026 | GACAGGGAGATCTGG[G/T]AGCCTCGGCCTCCAC | 1877 |
rs188481446 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2230584 | GGTTTGGGCACCAGG[C/T]GGAACCTGGCCTTGG | 1877 |
rs188680732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227178 | ACTACAGGTGCATGC[C/T]GCCACACTTCCACGC | 1877 |
rs188929679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225231 | AAGAAAAAAGATTGT[A/G]TGTCATGTGCCGAGA | 1877 |
rs189461001 | snp | C/T | 0.0217937 | 0.102088 | intron-variant | E4F1 | GRCh38.p7 | 16:2232374 | AAGACGGTGAGCCGG[C/T]GTGCGGGGAGCCAGT | 1877 |
rs189621252 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235731 | CTTTACAATAAAACA[C/T]GAGAACCTGCAGCTT | 1877 |
rs190273343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226483 | GGTGGCCCCTGCAGG[C/T]GAGTCATAGCTGTGG | 1877 |
rs190672620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230775 | CCAAGACACTCATCA[A/G]TGCCACTCAGAGCTC | 1877 |
rs191517583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224466 | ATTCTCATTTTGGGG[A/G]TGAGGAAAATCGAAG | 1877 |
rs191783987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2227618 | ACCTCATGATCCGCC[C/T]GCTTCAGCCTCCCAA | 1877 |
rs191847193 | snp | A/G | 0.00087146 | 0.0208559 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228412 | CCGCTGCCAGGCAGA[A/G]TTCACCGCCTTGGAG | 1877 |
rs191872870 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230001 | TGCCACCCCCTGGTT[C/T]CTGCTCCCTGCCCGT | 1877 |
rs192115590 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222487 | TTGCACTCCAGCCTA[A/G]GTGATAGAGTGAGAC | 1877 |
rs192315662 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | E4F1 | GRCh38.p7 | 16:2234043 | TGGGCTATAGGTGGC[C/T]GGGGTGCTTCTGGGT | 1877 |
rs192547239 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236186 | AGGGGCGAGGACAAG[A/G]ACACAGCCGCACCGG | 1877 |
rs192654052 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223101 | TGAGCCATCCCCGAC[C/T]CGTGTTCTTTTCCCG | 1877 |
rs193007268 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | E4F1 | GRCh38.p7 | 16:2230864 | GGATGGTGGCGTCAC[C/T]TGGGAGCATGAACTC | 1877 |
rs193133812 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225468 | AGTAAGACCCCGTCT[C/G]TATTTTCTTTTTTTT | 1877 |
rs193174002 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | E4F1 | GRCh38.p7 | 16:2230591 | GCACCAGGCGGAACC[A/T]GGCCTTGGGCAGCCC | 1877 |
rs199569337 | in-del | -/C | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229366 | CTGACCCTGGCCCGG[-/C]GGGTGAAGGGATTGG | 1877 |
rs199627791 | snp | C/T | 0.00113062 | 0.0237493 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232902 | AGCAAAGAGGACGCA[C/T]GTGCAGGTCAGCATG | 1877 |
rs199667792 | snp | C/T | 0.000117327 | 0.0076583 | intron-variant | E4F1 | GRCh38.p7 | 16:2232962 | GGCTGTGGACGCAGC[C/T]GCCACTGGGGTGTGT | 1877 |
rs199723355 | snp | C/G | 1.80896e-05 | 0.0030074 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235327 | ACGGCGCTGGGCCCA[C/G]AGGCGGCTGCCGCCG | 1877 |
rs199776709 | snp | A/G | 0.00181969 | 0.0301087 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233950 | CAGTGAGACCTTCCC[A/G]ACAGCAGCCACCCTG | 1877 |
rs199803798 | snp | A/G | 1.6659e-05 | 0.00288604 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232786 | AGTGCTCCAAGTGTG[A/G]AAAGAGCTTCCGGGA | 1877 |
rs199977994 | snp | A/C/G | 0.000139542 | 0.00835191 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235447 | GCCCGGGCAGGGACA[A/C/G]GTGGCACTGAACAGG | 1877 |
rs200030854 | snp | A/G | 6.85248e-05 | 0.00585301 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234201 | CCTGCGCGCAGTGTG[A/G]CAAGGCCTTCCCCAA | 1877 |
rs200055937 | snp | C/T | 1.66355e-05 | 0.002884 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233108 | CCTGGTGACAGATGC[C/T]AAGGGCACCGTCATC | 1877 |
rs200137506 | snp | A/G | 0.00105124 | 0.0229023 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235368 | CATCGCCACCCCCGA[A/G]AGCCTGACAGAGCAG | 1877 |
rs200190676 | snp | C/T | 0.000128787 | 0.00802353 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233441 | CCTCCCCTGCAGCCC[C/T]CCGTCTCCCAGGAGC | 1877 |
rs200233950 | snp | C/G/T | 0.00543149 | 0.05183 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233460 | TCTCCCAGGAGCTCC[C/G/T]CTGCTCCAGCGAGGG | 1877 |
rs200326283 | snp | A/G | 0.000630099 | 0.0177384 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229628 | CCCACATCGTGGTGG[A/G]GGCGGCCTCTCTGGC | 1877 |
rs200374361 | in-del | -/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225810 | AAAAAAAAAAAAAAA[-/T]AAAGGCTGGGCGCAA | 1877 |
rs200467051 | snp | C/T | 0.000116548 | 0.00763285 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235023 | GTGGGGCCCTGGGGC[C/T]GTGCTGGGACCCAGG | 1877 |
rs200493907 | snp | C/T | 0.000121396 | 0.00778995 | intron-variant | E4F1 | GRCh38.p7 | 16:2233840 | GGTACTGCCAGGGCA[C/T]AGCCTGCCCCGGGTG | 1877 |
rs200534216 | snp | C/T | 3.9797e-05 | 0.0044606 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234626 | ACCTGGAGGAGAAGC[C/T]GCACGTGTGCCAGTT | 1877 |
rs200695415 | snp | C/T | 0.000524733 | 0.0161892 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235606 | CTGGCCGGGCAGGGA[C/T]AGGGCAGAGGACTCT | 1877 |
rs200728691 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | E4F1 | GRCh38.p7 | 16:2225330 | CTGTACCCTCTGAGC[-/T]TTGTCCTATGAGGCT | 1877 |
rs200758185 | snp | A/G | 0.000798403 | 0.0199641 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234751 | GGCTTCGCCGAGCAC[A/G]GCACGCTGAACCGGC | 1877 |
rs200831818 | snp | A/C | 0.00110602 | 0.0234901 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223675 | AAGCCCAGGCCGAAG[A/C]CGGGCGGGAAGCGGG | 1877 |
rs200965712 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233053 | GGACAGCCACATCAT[C/T]GGTGACAGGCGAGCC | 1877 |
rs200987209 | snp | A/G | 0.000551503 | 0.0165966 | intron-variant | E4F1 | GRCh38.p7 | 16:2232941 | AGCTGCCTGGTCCTG[A/G]GGGCTGGCTGTGGAC | 1877 |
rs201011998 | snp | A/T | 0.00299549 | 0.0385846 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235369 | ATCGCCACCCCCGAG[A/T]GCCTGACAGAGCAGG | 1877 |
rs201223947 | snp | C/T | 0.000333463 | 0.0129081 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235527 | AGGCGAGCTGGTCAT[C/T]GCCTCGCCGGAGGGC | 1877 |
rs201269196 | snp | A/G | 0.000158662 | 0.00890537 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235162 | AGGGGTAGGGCAGGC[A/G]GGGGCGGGGAGGCTC | 1877 |
rs201296918 | snp | C/T | 0.00174368 | 0.0294754 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233637 | TACTGGAAGTGCAGC[C/T]GCTGGAGACAGTAGG | 1877 |
rs201442335 | snp | A/G | 1.72142e-05 | 0.00293374 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235392 | AGAGCAGGTGGCCAT[A/G]ACGCTGGCCTCGGCC | 1877 |
rs201499569 | snp | C/G | 1.67947e-05 | 0.00289777 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234273 | AGCGCCGCTTCCGCT[C/G]TGGCGACTGCGGGAA | 1877 |
rs201519515 | snp | C/T | 6.64044e-05 | 0.00576175 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232857 | TGCACAGAGAAAATC[C/T]GCTTCAGTGTGAGCA | 1877 |
rs201716081 | snp | C/T | 4.17232e-05 | 0.00456726 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233963 | CCGACAGCAGCCACC[C/T]TGGAGGCCCACAAGA | 1877 |
rs201773481 | snp | C/T | 0.000683875 | 0.0184789 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233047 | GCTTGGGGACAGCCA[C/T]ATCATCGGTGACAGG | 1877 |
rs201928284 | snp | C/T | 1.84599e-05 | 0.00303803 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235331 | CGCTGGGCCCAGAGG[C/T]GGCTGCCGCCGACAC | 1877 |
rs201979006 | snp | A/G | 7.65404e-05 | 0.00618582 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235024 | TGGGGCCCTGGGGCC[A/G]TGCTGGGACCCAGGG | 1877 |
rs202007289 | snp | A/T | 0.00114045 | 0.0238522 | intron-variant | E4F1 | GRCh38.p7 | 16:2228527 | CTGGGCCAGGAGGTG[A/T]GCCCTCACCCACTCC | 1877 |
rs202118148 | snp | A/G | 3.57079e-05 | 0.00422524 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235047 | ACCCAGGGGCAGCCA[A/G]GGCTGACCTCTGTCC | 1877 |
rs367646024 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222550 | AAAACCAAAAACAAC[C/T]CCCATCTCCAAAACC | 1877 |
rs367749621 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | E4F1 | GRCh38.p7 | 16:2229690 | GGTAAGCCGACTTCC[A/C]TGAATCGCTGGCCTG | 1877 |
rs367946733 | snp | C/G/T | 0.000138396 | 0.00831759 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228507 | CCCCTGCCACCACAG[C/G/T]GTTGCTGGGCCAGGA | 1877 |
rs367999348 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229859 | CGTTGGGCACTGGGC[C/T]TTCCTCAGGTGTCCA | 1877 |
rs368082034 | snp | A/C | 0.000159987 | 0.00894248 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233585 | GCTGCCGGGTCCAGT[A/C]CCCAGCCCCTGGCAG | 1877 |
rs368189091 | snp | C/T | 0.000258494 | 0.0113657 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235413 | GGCCTCGGCCATCAG[C/T]GAGGGCACTGTGCTT | 1877 |
rs368381184 | snp | A/G | 0.000153988 | 0.00877327 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233923 | GCCCAGGACCCACCC[A/G]TGTCCTCAGTGCAGT | 1877 |
rs368382659 | snp | C/T | 0.000425858 | 0.0145859 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233533 | CATCGTCCTTGAGCG[C/T]GCTGCTGGGGAGGAG | 1877 |
rs368408185 | snp | C/T | 0.000102124 | 0.00714504 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228379 | CGTTGCAGATGAGGA[C/T]GATGTGCACAGATGC | 1877 |
rs368692876 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227967 | CCATGCCCGGCCCCA[A/G]CAGTCTTAAATCCTG | 1877 |
rs368693289 | snp | A/C/G | 8.4334e-05 | 0.00649313 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234251 | CACCAGGAGGTGCAC[A/C/G]TGCGTGAGCGCCGCT | 1877 |
rs368730551 | snp | C/T | 0.00015819 | 0.00889214 | intron-variant, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234963 | GTGTTGGTGGAGTTC[C/T]CGTCCGTGGTAGCTG | 1877 |
rs368979736 | snp | A/G | 1.6676e-05 | 0.00288751 | intron-variant | E4F1 | GRCh38.p7 | 16:2229549 | ACAGACGACTCCCCT[A/G]TTTTCTTCCCCCTTT | 1877 |
rs368981200 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227322 | TGAAGTGATTCTCCT[A/G]CCTCAGCCTCTCGAA | 1877 |
rs369048199 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222372 | AATACAAAAATTAGC[C/T]GGCCATGGTGGTGCA | 1877 |
rs369105592 | snp | A/G | 0.000253235 | 0.0112496 | utr-variant-5-prime, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223576 | TTGTTATGACGACAT[A/G]GTCGTAAATCCGCCA | 1877 |
rs369250307 | snp | C/G | 1.66134e-05 | 0.00288208 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232881 | GTGAGCAAGGACGTG[C/G]TTGTCAGCAAAGAGG | 1877 |
rs369253796 | snp | C/G | 1.74388e-05 | 0.00295281 | intron-variant | E4F1 | GRCh38.p7 | 16:2232144 | CAGGGGCAGGTCCTG[C/G]GGCTTAGGCCCAGAT | 1877 |
rs369255809 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222914 | GTAGTCCCAGCTACT[C/T]AGGAGGCTGAGGCAG | 1877 |
rs369256860 | snp | G/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230412 | CTGCTGGGGTTGGGG[G/T]TGCGGCAGGGGCGAG | 1877 |
rs369274242 | snp | C/T | 1.66452e-05 | 0.00288484 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233117 | AGATGCCAAGGGCAC[C/T]GTCATCCACGAAGTC | 1877 |
rs369317092 | snp | A/G | 0.000133158 | 0.00815851 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233118 | GATGCCAAGGGCACC[A/G]TCATCCACGAAGTCC | 1877 |
rs369334404 | snp | C/T | 0.000100568 | 0.00709042 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233989 | CAAGAGGGGCCACAC[C/T]GGTAGGTGATGGGTG | 1877 |
rs369411860 | snp | C/T | 0.000285808 | 0.0119508 | intron-variant | E4F1 | GRCh38.p7 | 16:2232751 | TGACTAGGTTCTCTC[C/T]GCAGATGAGCGCCCC | 1877 |
rs369465221 | snp | C/T | 0.000210534 | 0.0102578 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235341 | AGAGGCGGCTGCCGC[C/T]GACACCATCACCATC | 1877 |
rs369469139 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222978 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 1877 |
rs369561300 | snp | C/T | 0.000927018 | 0.0215093 | intron-variant, synonymous-codon | E4F1 | GRCh38.p7 | 16:2228334 | TGGCTGCCCAGCCTC[C/T]GCCTTCCCAGGCCCT | 1877 |
rs369593675 | snp | C/T | 6.64386e-05 | 0.00576323 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229659 | AGCAGACATCAGCCA[C/T]GCATCTGACCTTGTT | 1877 |
rs369630364 | snp | A/G | 6.90107e-05 | 0.00587372 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235533 | GCTGGTCATCGCCTC[A/G]CCGGAGGGCCAGCTG | 1877 |
rs369695932 | snp | A/G | 1.67416e-05 | 0.00289318 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234302 | AAGCTCTACAAGACC[A/G]TTGCCCATGTGCGTG | 1877 |
rs369921174 | snp | A/C | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226636 | TGGAAGCAGAAGAAA[A/C]AGCTCCTATCCCTTT | 1877 |
rs369951581 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235167 | TAGGGCAGGCGGGGG[C/T]GGGGAGGCTCCCTGG | 1877 |
rs370107044 | snp | A/G | 1.66466e-05 | 0.00288496 | splice-donor-variant | E4F1 | GRCh38.p7 | 16:2229676 | CATCTGACCTTGTTG[A/G]TAAGCCGACTTCCAT | 1877 |
rs370129492 | snp | A/G | 2.17143e-05 | 0.00329495 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223658 | GGCCGCTCATACGGC[A/G]GAAGCCCAGGCCGAA | 1877 |
rs370199008 | snp | A/C | 0.000153988 | 0.00877327 | intron-variant | E4F1 | GRCh38.p7 | 16:2232370 | CTTCAAGACGGTGAG[A/C]CGGCGTGCGGGGAGC | 1877 |
rs370269815 | snp | C/T | 0.000159987 | 0.00894249 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234902 | GCTGGTGTCTGAGGA[C/T]AGCCCCGCGGCAGCC | 1877 |
rs370499012 | snp | C/T | | | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232818 | TCGGGTGCACTGACC[C/T]GGCACCTCAAGTCTC | 1877 |
rs370510459 | snp | C/T | 1.72994e-05 | 0.00294099 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235092 | CCAGGCCACTGCGGA[C/T]GATGCGGAGACCAGT | 1877 |
rs370525100 | snp | C/G | 0.00044396 | 0.0148924 | intron-variant | E4F1 | GRCh38.p7 | 16:2232451 | TGCCACGCCCTCCCC[C/G]ACAGGGCAGCATCCT | 1877 |
rs370540960 | snp | A/G | 0.000709268 | 0.0188184 | intron-variant | E4F1 | GRCh38.p7 | 16:2232953 | CTGGGGGCTGGCTGT[A/G]GACGCAGCCGCCACT | 1877 |
rs370544239 | snp | C/G/T | 5.22656e-05 | 0.0051118 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235316 | TGGACGAGGAGACGG[C/G/T]GCTGGGCCCAGAGGC | 1877 |
rs370653709 | snp | A/G | 0.00122986 | 0.0247673 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233596 | CAGTCCCCAGCCCCT[A/G]GCAGTGGCAGCCCCG | 1877 |
rs370693095 | snp | G/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2233306 | TGGGCTTCCCACAGG[G/T]AGAGCAGGGCCAGTG | 1877 |
rs370702358 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | E4F1 | GRCh38.p7 | 16:2231205 | AGGTCCTGTCTTTGC[A/G]GGTGCAGGGGTGCGG | 1877 |
rs370764054 | snp | C/T | 2.50636e-05 | 0.00353994 | synonymous-codon, stop-gained, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223691 | CGGGCGGGAAGCGGG[C/T]GAGGGTGCAGTTGCG | 1877 |
rs370872113 | snp | C/G | 3.32862e-05 | 0.00407946 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232908 | GAGGACGCACGTGCA[C/G]GTCAGCATGGTGCGG | 1877 |
rs370894816 | in-del | -/A | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226109 | AAGAAAAAAAAAAAA[-/A]GATGCAGATTGGGTC | 1877 |
rs370942286 | snp | A/G/T | 9.96808e-05 | 0.00705916 | intron-variant | E4F1 | GRCh38.p7 | 16:2232375 | AGACGGTGAGCCGGC[A/G/T]TGCGGGGAGCCAGTG | 1877 |
rs371012550 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231731 | CTGCAGTGGCCCAGC[C/T]CATCTCCTCCGATGG | 1877 |
rs371113367 | snp | A/G | 0.000336274 | 0.0129624 | intron-variant | E4F1 | GRCh38.p7 | 16:2233189 | GGCCCCAGAGGTGGG[A/G]GCGACGGGGGGCCCC | 1877 |
rs371173319 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225322 | AGCTTGGGTCTGTAC[C/G]CTCTGAGCTTGTCCT | 1877 |
rs371251950 | snp | A/G | 1.66233e-05 | 0.00288295 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232887 | AAGGACGTGGTTGTC[A/G]GCAAAGAGGACGCAC | 1877 |
rs371289726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228755 | CCTCTGGTCGAAGCC[C/T]GTGCTGTTGGGGGCC | 1877 |
rs371302779 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | E4F1 | GRCh38.p7 | 16:2227878 | TATGTTGACCAGGCT[C/T]GTCTTGAACTCCTGG | 1877 |
rs371317212 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223540 | CTTGCCGTTCCCTCA[C/G]GCTGGCCTCGGCGCG | 1877 |
rs371327894 | snp | C/G | 2.23082e-05 | 0.0033397 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223606 | ATCTTCCTGCGGCGC[C/G]TTGCGACATGGAGGG | 1877 |
rs371331210 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230541 | CGGGGCTGAGGCAGG[C/T]GGGGAGTGGGCAGCT | 1877 |
rs371440042 | snp | A/C/T | 8.85283e-05 | 0.00665261 | intron-variant | E4F1 | GRCh38.p7 | 16:2232606 | CCTCGGGCTGGAGCC[A/C/T]GGTAGCACCCCGATG | 1877 |
rs371527360 | snp | A/G | 7.02502e-05 | 0.00592623 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235536 | GGTCATCGCCTCGCC[A/G]GAGGGCCAGCTGGAG | 1877 |
rs371666989 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229436 | CACCCCAGCCGTCCC[A/G]AGGACGTGGACCCAG | 1877 |
rs371734250 | snp | A/G | 5.41658e-05 | 0.00520384 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235477 | GCCACTGTGACCATG[A/G]TGTCATCAGAGGACA | 1877 |
rs371822192 | snp | G/T | 0.000174663 | 0.00934351 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228514 | CACCACAGCGTTGCT[G/T]GGCCAGGAGGTGAGC | 1877 |
rs371833339 | snp | G/T | 0.000218886 | 0.0104592 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235037 | CCGTGCTGGGACCCA[G/T]GGGCAGCCAAGGCTG | 1877 |
rs371851922 | snp | A/G | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234756 | CGCCGAGCACGGCAC[A/G]CTGAACCGGCACCTG | 1877 |
rs371870350 | snp | C/T | 4.98583e-05 | 0.00499266 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233084 | TATAGAGACTTCACC[C/T]GTGATTCACCTGGTG | 1877 |
rs372004326 | snp | C/G | 0.000153988 | 0.00877327 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233928 | GGACCCACCCATGTC[C/G]TCAGTGCAGTGAGAC | 1877 |
rs372071032 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | E4F1 | GRCh38.p7 | 16:2229725 | ACCTTCGTGGTTGGG[A/G]CCAGAGGATGGGGCC | 1877 |
rs372248982 | snp | A/G | 1.66921e-05 | 0.00288891 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233011 | CACTCCACCTTGAAG[A/G]TTCTGGAGCTGGAGC | 1877 |
rs372279499 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223350 | CATAGGTCCTTCTGC[C/T]GCCCCGCCCCCTGGC | 1877 |
rs372298010 | snp | C/T | 5.09507e-05 | 0.00504705 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228382 | TGCAGATGAGGACGA[C/T]GTGCACAGATGCGGC | 1877 |
rs372319086 | snp | C/T | 1.65855e-05 | 0.00287967 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229600 | CCAGGCCCAGAGGAG[C/T]CCATCACTGTGGCCC | 1877 |
rs372466046 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229803 | AGGGGCCGCGGCCTC[A/G]TGGCAGCCTTTCTGC | 1877 |
rs372469137 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222379 | AAATTAGCTGGCCAT[A/G]GTGGTGCACTCCTGT | 1877 |
rs372658146 | snp | A/G | 0.000550766 | 0.0165855 | intron-variant, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234969 | GTGGAGTTCTCGTCC[A/G]TGGTAGCTGACACCC | 1877 |
rs372663046 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | E4F1 | GRCh38.p7 | 16:2233708 | AGGGGCTGTCCCCAC[A/G]CTGGCCTTCGCCTCC | 1877 |
rs372690984 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2234044 | GGGCTATAGGTGGCC[A/G]GGGTGCTTCTGGGTG | 1877 |
rs372723793 | snp | G/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222993 | CGCCACTGCACTCCA[G/T]CCTGGGCGATAGAAA | 1877 |
rs372816133 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231048 | GATTTTCCCCTTTGC[A/G]GGCATCCTGGGTACT | 1877 |
rs372896150 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | E4F1 | GRCh38.p7 | 16:2232752 | GACTAGGTTCTCTCT[A/G]CAGATGAGCGCCCCT | 1877 |
rs372959140 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | E4F1 | GRCh38.p7 | 16:2232372 | TCAAGACGGTGAGCC[A/G]GCGTGCGGGGAGCCA | 1877 |
rs373086605 | snp | A/G | 0.00010651 | 0.00729681 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235181 | GCGGGGAGGCTCCCT[A/G]GCACAGCCGCTCTTG | 1877 |
rs373113928 | snp | C/T | 0.000258873 | 0.0113741 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234402 | AGGTGGGTCTCTGGC[C/T]GCAGGACCCTGGCGC | 1877 |
rs373165341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231265 | CCAGGCCCTCCTGCC[A/G]CTTCGCGGAAAAAGT | 1877 |
rs373212668 | snp | A/C | 4.02779e-05 | 0.00448746 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234617 | TCAGGACACACCTGG[A/C]GGAGAAGCCGCACGT | 1877 |
rs373356413 | snp | A/G | 3.7035e-05 | 0.00430304 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235597 | TGCGGGGTCCTGGCC[A/G]GGCAGGGACAGGGCA | 1877 |
rs373359809 | snp | C/T | 5.32212e-05 | 0.00515827 | intron-variant | E4F1 | GRCh38.p7 | 16:2233191 | CCCCAGAGGTGGGGG[C/T]GACGGGGGGCCCCGG | 1877 |
rs373362876 | in-del | GG/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229370 | ACCCTGGCCCGGGGG[GG/T]GAAGGGATTGGACTG | 1877 |
rs373383344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224372 | GGGGCGGCGGCTTCT[A/G]CCAGTAATGTAACAA | 1877 |
rs373465934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226708 | CCTTGAACTTCAGGT[C/G]ATTTTCCTAGGATGG | 1877 |
rs373679522 | snp | A/G | 3.37587e-05 | 0.00410831 | intron-variant | E4F1 | GRCh38.p7 | 16:2232955 | GGGGGCTGGCTGTGG[A/G]CGCAGCCGCCACTGG | 1877 |
rs373733992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228951 | CTTTGCTGAGCCCCA[C/T]GCCCAGCTTGGGCTG | 1877 |
rs373873519 | snp | C/T | 3.55221e-05 | 0.00421424 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235183 | GGGGAGGCTCCCTGG[C/T]ACAGCCGCTCTTGCT | 1877 |
rs373947740 | snp | C/T | 5.22207e-05 | 0.00510956 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235305 | GAACGTCACCATGGA[C/T]GAGGAGACGGCGCTG | 1877 |
rs374094183 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222074 | AAAATATAAAAAAAT[C/T]AGCCGGGTGTGGTGG | 1877 |
rs374158929 | snp | A/G | 0.000155988 | 0.00883005 | intron-variant | E4F1 | GRCh38.p7 | 16:2232138 | TCTGGACAGGGGCAG[A/G]TCCTGGGGCTTAGGC | 1877 |
rs374328393 | snp | C/G/T | 8.1074e-05 | 0.00636642 | intron-variant | E4F1 | GRCh38.p7 | 16:2232378 | CGGTGAGCCGGCGTG[C/G/T]GGGGAGCCAGTGTGT | 1877 |
rs374336568 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230179 | CCCTCTGGTGTGGGA[A/G]TGGTGATTGCTACAC | 1877 |
rs374373444 | snp | C/T | 0.000202999 | 0.0100727 | intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234998 | CCAGGAGTATATCAT[C/T]GAGGTGGGTGTGGGG | 1877 |
rs374483220 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227903 | TCCTGGGCTCAAGCT[A/G]TCCTCCCACCTTGGC | 1877 |
rs374527304 | snp | C/T | 5.02449e-05 | 0.00501198 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234290 | GGCGACTGCGGGAAG[C/T]TCTACAAGACCATTG | 1877 |
rs374607484 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221629 | GAACTCCTGATGTCA[A/G]GTGATCCACCCACCT | 1877 |
rs374662668 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | E4F1 | GRCh38.p7 | 16:2230349 | GATGCTTGTGCAGGG[A/G]GGCATTCAGAGGCAG | 1877 |
rs374688881 | snp | C/T | 0.000153988 | 0.00877327 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235104 | GGACGATGCGGAGAC[C/T]AGTGAGGCCACGGAG | 1877 |
rs374700250 | snp | G/T | 0.000104488 | 0.00722724 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234924 | GCGGCAGCCACCACC[G/T]TCCTCACGGAAGACC | 1877 |
rs374841967 | snp | A/C/G | 6.37681e-05 | 0.00564623 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223624 | GCGACATGGAGGGCG[A/C/G]GATGGCAGTGCGGGT | 1877 |
rs374882960 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222855 | GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 1877 |
rs374926049 | snp | C/T | 0.00104763 | 0.022863 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235066 | TGACCTCTGTCCTTC[C/T]GCCCATCTGCCCAGG | 1877 |
rs374927912 | snp | C/T | 5.05753e-05 | 0.00502843 | utr-variant-5-prime, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223575 | GTTGTTATGACGACA[C/T]GGTCGTAAATCCGCC | 1877 |
rs374937976 | snp | C/G | 1.66868e-05 | 0.00288845 | intron-variant | E4F1 | GRCh38.p7 | 16:2229544 | AGCATACAGACGACT[C/G]CCCTGTTTTCTTCCC | 1877 |
rs374953286 | snp | A/C/T | 0.00105042 | 0.0228947 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233126 | GGGCACCGTCATCCA[A/C/T]GAAGTCCACGTCCAG | 1877 |
rs374969325 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | E4F1 | GRCh38.p7 | 16:2233814 | AGGGTGGGGCCCATG[A/G]TTGTGTTCTTGGTAC | 1877 |
rs375039813 | snp | A/G | 0.000323102 | 0.0127062 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233576 | CCAGCTCCTGCTGCC[A/G]GGTCCAGTCCCCAGC | 1877 |
rs375148567 | snp | A/G | 5.311e-05 | 0.00515288 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235204 | CGCTCTTGCTGAGCC[A/G]TGGCCCTGCAGGTGG | 1877 |
rs375170561 | snp | C/T | 8.58369e-05 | 0.00655066 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234649 | TGCCAGTTCTGCAGC[C/T]GTGGCTTCCGAGAGA | 1877 |
rs375178489 | snp | C/T | 0.000118468 | 0.00769546 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232223 | GGCGGAGCTGGGAGA[C/T]GGTGAGATGGCCGAG | 1877 |
rs375194455 | snp | C/G/T | 3.31985e-05 | 0.00407411 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232833 | CGGCACCTCAAGTCT[C/G/T]TCACCCCCTGCACAG | 1877 |
rs375309480 | snp | C/G/T | 3.33975e-05 | 0.0040863 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233026 | GTTCTGGAGCTGGAG[C/G/T]TGCCGGCTTGGGGAC | 1877 |
rs375358824 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228425 | GAGTTCACCGCCTTG[A/G]AGGATTTTGTTCAGC | 1877 |
rs375397955 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222206 | TAGCCTAGGTGACAG[A/G]GCGAGACTCCATCTC | 1877 |
rs375407226 | snp | C/G | 0.000173569 | 0.0093142 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228365 | GCTGACAGCAGGCTC[C/G]TTGCAGATGAGGACG | 1877 |
rs375530655 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223867 | CGGGCTCGACCGACC[C/T]TCCCAGACCCAGACA | 1877 |
rs375602180 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | E4F1 | GRCh38.p7 | 16:2233364 | CACAAGGCTCCTGGC[A/G]TGCGTCTGCCCCATG | 1877 |
rs375723167 | snp | A/G | 0.000106187 | 0.00728576 | intron-variant | E4F1 | GRCh38.p7 | 16:2232607 | CTCGGGCTGGAGCCC[A/G]GTAGCACCCCGATGG | 1877 |
rs376064191 | snp | C/G | 0.000792575 | 0.0198912 | intron-variant | E4F1 | GRCh38.p7 | 16:2228542 | AGCCCTCACCCACTC[C/G]CCCATCCCCTCCCGG | 1877 |
rs376235056 | snp | C/G | | | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229675 | GCATCTGACCTTGTT[C/G]GTAAGCCGACTTCCA | 1877 |
rs376359524 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223708 | GGGTGCAGTTGCGGC[-/G]GGTGGCGGCGGCCTT | 1877 |
rs376712603 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226920 | CAGCTCCCTGCATTT[C/G]CCTCTCAGCCAGAGC | 1877 |
rs376798905 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2234075 | TCCAGGGTGGGTCCA[C/T]AGACAGCAGGGAGCC | 1877 |
rs376804356 | snp | A/C/T | 0.000122401 | 0.00782221 | utr-variant-3-prime, missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235266 | CGTGCACCAGGCTAG[A/C/T]GCCGGCCACCAGATC | 1877 |
rs376901022 | snp | C/G | 1.66988e-05 | 0.00288949 | intron-variant | E4F1 | GRCh38.p7 | 16:2229688 | TTGGTAAGCCGACTT[C/G]CATGAATCGCTGGCC | 1877 |
rs377092233 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229391 | GATTGGACTGGGACC[A/G/T]GTGGTCGTGTTGGGG | 1877 |
rs377234026 | snp | C/T | 0.00373028 | 0.0430258 | intron-variant | E4F1 | GRCh38.p7 | 16:2233850 | GGGCACAGCCTGCCC[C/T]GGGTGCTGGAGACCT | 1877 |
rs377249962 | snp | C/G/T | 0.00121132 | 0.0245829 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234415 | GCCGCAGGACCCTGG[C/G/T]GCCTGATCCCCCCAT | 1877 |
rs377282911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225374 | CACTGTGGCTCATAC[C/G]TGTAACCCCAACACT | 1877 |
rs377409835 | snp | C/T | 2.25309e-05 | 0.00335633 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223669 | CGGCAGAAGCCCAGG[C/T]CGAAGCCGGGCGGGA | 1877 |
rs377473883 | snp | C/T | 0.000112911 | 0.00751285 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234750 | TGGCTTCGCCGAGCA[C/T]GGCACGCTGAACCGG | 1877 |
rs377483446 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226504 | ATAGCTGTGGTTTGG[C/T]CCTTTCTCCGCCCTC | 1877 |
rs377572921 | snp | A/G | 0.000191573 | 0.00978517 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235314 | CATGGACGAGGAGAC[A/G]GCGCTGGGCCCAGAG | 1877 |
rs377655467 | snp | A/C/G | 4.98893e-05 | 0.00499425 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232895 | GGTTGTCAGCAAAGA[A/C/G]GACGCACGTGCAGGT | 1877 |
rs527240399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226053 | AGCTGAGATCGCCCC[A/G]CTGCACTCCAGCCTG | 1877 |
rs527420469 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235962 | CTGGAGCTGTGCCCC[C/T]AGCTGCGCTGCCTGA | 1877 |
rs527623336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2226581 | GGGTTTGATCCTGCC[A/G]AGGGACTGAAGGTGA | 1877 |
rs527754725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225338 | CTCTGAGCTTGTCCT[A/G]TGAGGCTGCAGATGG | 1877 |
rs527815095 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225627 | TACGGCACGCGGCAT[C/T]ACACCCGGCTAATTT | 1877 |
rs527879308 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235678 | GCACAGGATGGAGGC[A/G]CCCCAAGACGGACAG | 1877 |
rs528154117 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222164 | GAGGCGGAGATTGCA[C/G]TGAACCAAGATCGTG | 1877 |
rs528212883 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221553 | CGTGCACCACCACAC[C/G]CAGATAATTTTTGTA | 1877 |
rs528618207 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | E4F1 | GRCh38.p7 | 16:2227815 | CTAAATGTTTAACAA[C/T]GTTTTAAAAACTTTT | 1877 |
rs528770998 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231559 | TGAACTGTGTTTACA[A/G]CCTAGCTTTGCACAT | 1877 |
rs528812715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2232750 | CTGACTAGGTTCTCT[C/T]TGCAGATGAGCGCCC | 1877 |
rs528812934 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233646 | TGCAGCCGCTGGAGA[C/T]AGTAGGTGCCAGCAC | 1877 |
rs529037675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225386 | TACCTGTAACCCCAA[C/G]ACTTTGGGAGGCTGA | 1877 |
rs529097249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230447 | TAGGTGTGCAGACGC[A/G]AGGGAAGGAGCTGTC | 1877 |
rs529237766 | snp | A/G | 0.000103908 | 0.00720716 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235516 | CTGGAGCATGCAGGC[A/G]AGCTGGTCATCGCCT | 1877 |
rs529305808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228997 | GAACCCCGCACACGC[C/T]GCAGCGGGCGCTTGT | 1877 |
rs529404877 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231204 | CAGGTCCTGTCTTTG[A/C/T]GGGTGCAGGGGTGCG | 1877 |
rs529417951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2234041 | GATGGGCTATAGGTG[C/G]CCGGGGTGCTTCTGG | 1877 |
rs529658042 | snp | A/G/T | 4.49691e-05 | 0.00474157 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223744 | CCAGCGGCTTCCTCG[A/G/T]CCTCCCGGCGCCCTT | 1877 |
rs529675186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226669 | GTAAACAGGTACTGT[C/T]CCTGACACTCAGCCG | 1877 |
rs529712952 | snp | C/T | 1.82673e-05 | 0.00302214 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232530 | GCTCTGTGGGGCCTC[C/T]TTCCGCACCAAGGGC | 1877 |
rs529907238 | snp | A/G | 0.0011001 | 0.0234273 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235270 | CACCAGGCTAGCGCC[A/G]GCCACCAGATCATCG | 1877 |
rs530255666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2225847 | GCGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 1877 |
rs530565857 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222947 | GAATGGCGTGAACCC[A/G]GGAGGCAGAGCTTGC | 1877 |
rs530921933 | snp | A/G | 1.71281e-05 | 0.00292639 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233169 | TCCCTGGGCATGAAA[A/G]CCCTGGCCCCAGAGG | 1877 |
rs531092764 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222240 | AAACAAAAACAGGCC[A/G]GGCGCGGTGGCTCAT | 1877 |
rs531141181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227959 | GTGAGCCACCATGCC[C/T]GGCCCCAGCAGTCTT | 1877 |
rs531154006 | snp | C/T | 0.000136075 | 0.00824737 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228474 | GCCAGCGGGCCCCTC[C/T]GGAGGCCCTGCCTGC | 1877 |
rs531263988 | snp | A/C/T | 4.86784e-05 | 0.00493324 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233480 | TCCAGCGAGGGCAGC[A/C/T]GTGAGAACCTGCTGC | 1877 |
rs531343828 | snp | C/T | 7.32681e-05 | 0.00605216 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235596 | CTGCGGGGTCCTGGC[C/T]GGGCAGGGACAGGGC | 1877 |
rs531567346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224489 | AATCGAAGGTTGGAG[A/G]CCTGAAAGTGACCGG | 1877 |
rs531619455 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | E4F1 | GRCh38.p7 | 16:2229787 | CCAGGGCCTGGCTGG[A/G]AGGGGCCGCGGCCTC | 1877 |
rs531668569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225496 | TTTTTTTTTTGAGAC[A/G]GCGTTTCTCTCTTGT | 1877 |
rs531872577 | in-del | -/T | 0.286303 | 0.24735 | intron-variant | E4F1 | GRCh38.p7 | 16:2227827 | CAATGTTTTAAAAAC[-/T]TTTTTTTTTTTTTTT | 1877 |
rs532002945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227673 | CACCGCCCTAATTTT[A/G]TATTTTTAGTAGAGA | 1877 |
rs532583403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2232010 | ACCTGGAGAGGTGAA[C/T]GGGACCTTGGCTGTT | 1877 |
rs532913024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2229868 | CTGGGCCTTCCTCAG[A/G]TGTCCACAGTGGCCG | 1877 |
rs532973687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229495 | AGCTTTACACTGGCA[A/G]AGCCCAGGCCTCTTC | 1877 |
rs532995496 | snp | A/G/T | 5.26607e-05 | 0.00513104 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235239 | CCACATCATGAAGGT[A/G/T]GTGCAGCAGATCGTG | 1877 |
rs533083336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2231664 | GAGAGCGTTCACTCT[C/T]CCAGGCCAAGCCTGC | 1877 |
rs533127513 | snp | C/T | 0.000118918 | 0.00771004 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233917 | AGCGGTGCCCAGGAC[C/T]CACCCATGTCCTCAG | 1877 |
rs533250705 | snp | C/T | | | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228362 | CCTGCTGACAGCAGG[C/T]TCGTTGCAGATGAGG | 1877 |
rs533283493 | snp | A/G | 0.00487728 | 0.0491411 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234791 | CCAAAGGTCTGGGCC[A/G]GTGGAGGTGGGAGGG | 1877 |
rs533310718 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | E4F1 | GRCh38.p7 | 16:2225825 | AAAAGGCTGGGCGCA[A/T]TGGCTCGCGCCTGTA | 1877 |
rs533493160 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222467 | GCTGCAGTGAGATCG[C/T]GCCATTGCACTCCAG | 1877 |
rs533708644 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | E4F1 | GRCh38.p7 | 16:2228935 | ATCAGCAAATGGCCA[C/T]CTTTGCTGAGCCCCA | 1877 |
rs533903373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224975 | CCCAGCACTTTGGGA[A/G]GCCAAGGTGGGTGGA | 1877 |
rs533919214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230645 | AGGGGGTGGAGGAGC[C/T]GTGGCGGAGGCCAAC | 1877 |
rs534584392 | snp | C/T | 6.76224e-05 | 0.00581435 | intron-variant | E4F1 | GRCh38.p7 | 16:2232956 | GGGGCTGGCTGTGGA[C/T]GCAGCCGCCACTGGG | 1877 |
rs534689979 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2226361 | TTCAGTGGCAATGCC[C/G]TGGAGCCGAGTGAGA | 1877 |
rs534774309 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236153 | TCAGGGAGGCAGAGT[C/T]TAGGCGACCTAATTT | 1877 |
rs534808087 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221764 | GGAGTTCTATAGCAG[C/T]CTAGGCAACATGGCA | 1877 |
rs534812287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228167 | GAGGGTGGGTCTGGC[C/T]CCTGCAGACCTGCAG | 1877 |
rs534827168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2233318 | AGGGAGAGCAGGGCC[A/G]GTGGGAGCGCCATGG | 1877 |
rs535007953 | snp | A/G | 3.49852e-05 | 0.00418227 | intron-variant | E4F1 | GRCh38.p7 | 16:2232133 | GGGTCTCTGGACAGG[A/G]GCAGGTCCTGGGGCT | 1877 |
rs535013880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226823 | TCTCTTCTGCACGAC[C/T]GGGGTCCGGCACAGC | 1877 |
rs535391582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2223982 | CCTGTCATCCCCCCT[C/T]TCTGGTGTGCGTCCA | 1877 |
rs535438537 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2229208 | GCCCTCTCCTCACAC[C/T]GCTCTGCCGGATGTG | 1877 |
rs535609007 | snp | C/T | 4.0312e-05 | 0.00448936 | intron-variant | E4F1 | GRCh38.p7 | 16:2228565 | CCTCCCGGGTTCACC[C/T]GACAGGTGGGGGAGG | 1877 |
rs535658342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224676 | GCGGGCGCCTGTAGT[C/G]GGGAGGCTGAGGCGG | 1877 |
rs535759108 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229796 | GGCTGGGAGGGGCCG[C/T]GGCCTCGTGGCAGCC | 1877 |
rs535986793 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221873 | AGAGGCTGCAGTGAG[C/T]TGAGATCACGGCACT | 1877 |
rs536442670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225686 | CATGTTGGCCAGGCT[A/G]GTCTTGAACTCCCGA | 1877 |
rs536454671 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2230809 | ATGTTCATGTGGGAG[G/T]TGGGGCGGGCTCTGG | 1877 |
rs536516786 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235730 | GCTTTACAATAAAAC[A/G]TGAGAACCTGCAGCT | 1877 |
rs536833832 | snp | A/C | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231371 | TCACTCCTGGGGCAT[A/C]GAGCGTGTAAGGGCT | 1877 |
rs536849171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231299 | CGTCTCCTCTGGCCT[C/T]GCAGCAGCCATGTTC | 1877 |
rs536922221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2233669 | GCCAGCACCACCTGC[A/G]GGCTCCTCCCAGGGC | 1877 |
rs536925571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2230273 | GAAGATGTCTCTCTC[C/T]CTGATGTGCTGTGGG | 1877 |
rs537259861 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | E4F1 | GRCh38.p7 | 16:2228632 | CGGGGGCCACGTGGG[C/T]GGGCAGAGGGCAGGC | 1877 |
rs537267947 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221607 | CCATGTTGGCCTGCT[G/T]GGTCTTGAACTCCTG | 1877 |
rs537401958 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224079 | GCCCTTCTCTGCCTC[C/G]GATGCCTGAGCCTGG | 1877 |
rs537442534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224778 | GCAGAGCCGGACTCC[C/G]TCTCAAAAGAAAAGA | 1877 |
rs537451589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227465 | CAAGCTCTGCCTGCC[C/G]GGTTCATGCCATTCT | 1877 |
rs537851333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230096 | TGGGTACAGGGTGGA[C/T]GGGACTCTCCCGCCT | 1877 |
rs537862010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224210 | GCTCTGGGCCTGTCC[C/G]TAGGGAGGCAGCAGA | 1877 |
rs537873850 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223095 | TACCCATGAGCCATC[C/T]CCGACCCGTGTTCTT | 1877 |
rs537989253 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223295 | CCAGTCCGCTCGCCC[C/G]TCGCGTTCTCTGGCT | 1877 |
rs538365814 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224503 | GACCTGAAAGTGACC[C/G]GGTGGGCTGGGTGCG | 1877 |
rs538432324 | snp | C/G | 2.13018e-05 | 0.0032635 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235013 | CGAGGTGGGTGTGGG[C/G]CCCTGGGGCCGTGCT | 1877 |
rs538648342 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235774 | CAGTGGCAGCCTCCG[C/T]GGCTGGTGCCACCAC | 1877 |
rs538862711 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2226213 | TGCCTTTTTTCCTTG[A/C]CCCTTCTCGTTCCAG | 1877 |
rs538906906 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221546 | TTACACGCGTGCACC[A/G]CCACACCCAGATAAT | 1877 |
rs539015855 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236080 | CAGCAGGAGATGCTG[G/T]GTAGGGAGTGTGGCT | 1877 |
rs539057194 | snp | C/T | 0.000184925 | 0.00961396 | intron-variant | E4F1 | GRCh38.p7 | 16:2234156 | GGCTTGGCCTGATGC[C/T]GTGTGTGGCTGCAGG | 1877 |
rs539199880 | snp | G/T | 0.000314317 | 0.0125323 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223822 | GGGCAGTTCATCCCG[G/T]GCTGGCAGAGGCCCG | 1877 |
rs539378764 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | E4F1 | GRCh38.p7 | 16:2229183 | AAGGCCTCTGGCCCA[C/T]ACCTCCAGGGCCCTC | 1877 |
rs539424232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2233787 | TTCCCTGGGGCCACA[A/G]GGGAGCCTGCCAGGG | 1877 |
rs539773841 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221753 | GCTTGAACTCAGGAG[C/T]TCTATAGCAGCCTAG | 1877 |
rs539854524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228100 | AGCCTTAGCAGGTCC[C/T]TGCAGCCTAAGCGTG | 1877 |
rs539965437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227497 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAT | 1877 |
rs539965441 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2233255 | GTCTTTGTTCTGGGC[A/G]CTGGCTCCAGGGGTC | 1877 |
rs540038120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230416 | TGGGGTTGGGGGTGC[A/G]GCAGGGGCGAGTGGC | 1877 |
rs540243236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234519 | CCTTGGGCCACAGGC[A/G]GGAGGGGAGAGCTGT | 1877 |
rs540405594 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235843 | CCACTCCTAGACTCA[C/T]GTGCCTGGCCGCCCC | 1877 |
rs540461168 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222614 | GCCTGTCATCCTAGC[A/G]CTTTGGGAGGCCGAA | 1877 |
rs540714147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231940 | ATTTAGGGGCCCTGG[A/G]GCATCTCTGGGCAGC | 1877 |
rs540780876 | snp | A/G | 1.73192e-05 | 0.00294267 | synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235126 | GCCACGGAGATCATC[A/G]AGGGCACCCAGACAG | 1877 |
rs540822546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224305 | GCTTTCTAGTTCTTT[A/G]ATCCTGGGTAGGTGA | 1877 |
rs540895897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229347 | GAGGTGTGAGAGTGA[C/T]GGCGCTGACCCTGGC | 1877 |
rs541004611 | snp | A/G | 2.06969e-05 | 0.00321683 | intron-variant | E4F1 | GRCh38.p7 | 16:2232434 | CCAGGAGGGCCCTGA[A/G]CTGCCACGCCCTCCC | 1877 |
rs541095921 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225368 | GCTGGGCACTGTGGC[A/T]CATACCTGTAACCCC | 1877 |
rs541204253 | snp | C/T | 0.0126979 | 0.078662 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235884 | TTCTGCCAGCCCTGG[C/T]GGCGCCTTGGTGCTG | 1877 |
rs541301791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227009 | ACATGCTCCAGGGCA[C/T]GCTCAAACTCCCGCA | 1877 |
rs541486521 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | E4F1 | GRCh38.p7 | 16:2231005 | TCAGCAGCCCCTCTT[G/T]GCACCCCTGCCACTC | 1877 |
rs541498247 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222176 | GCAGTGAACCAAGAT[C/T]GTGCCGTTGCATTCT | 1877 |
rs541525310 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227697 | GTAGAGATGGGATTT[C/T]ACCATATTGGTCAGG | 1877 |
rs541530140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228808 | TGGAGGGTCTCCTTT[A/G]GCTCTGGGGTACCAT | 1877 |
rs542125740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227520 | GGGACTATAGGCACC[G/T]GCCACCATGCCTGGC | 1877 |
rs542286926 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224723 | GGGAGGTGGAGCTTG[C/T]GGTGAGCCGAGACCG | 1877 |
rs542396099 | snp | A/G | 3.38587e-05 | 0.00411439 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228465 | AGAAGGCCTGCCAGC[A/G]GGCCCCTCCGGAGGC | 1877 |
rs542505220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231094 | GCCAGTCAGCAGGCC[C/T]GGTGGGCTTAGTCCA | 1877 |
rs542642756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229778 | CTCCCGAGACCAGGG[A/C]CTGGCTGGGAGGGGC | 1877 |
rs542672426 | snp | A/G | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234745 | GGCCGTGGCTTCGCC[A/G]AGCACGGCACGCTGA | 1877 |
rs542924573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224410 | TCCTGCTTTAGGTTT[C/T]TTCATTCTCAAACCA | 1877 |
rs542965861 | snp | A/G | 5.59362e-05 | 0.00528819 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235567 | GTGCAGACGGTCATC[A/G]TCTAGCATGAGGTCT | 1877 |
rs543017512 | snp | A/G/T | 0.000804165 | 0.0200383 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233036 | TGGAGCTGCCGGCTT[A/G/T]GGGACAGCCACATCA | 1877 |
rs543079123 | snp | C/T | 0.000181544 | 0.00952571 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232534 | TGTGGGGCCTCCTTC[C/T]GCACCAAGGGCTCAC | 1877 |
rs543217345 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2225154 | GGAGACGGAGGTCGC[A/G]GTAAGCCGAGATCGC | 1877 |
rs543263895 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222014 | CACCTGAGGTCAGGA[A/G]TTCAAAACCAGCATG | 1877 |
rs543477747 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230821 | GAGGTGGGGCGGGCT[C/T]TGGCCTTGACCTGGC | 1877 |
rs543683068 | snp | C/T | 0.000603384 | 0.0173588 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233890 | TCCCCAGCAGGTGGC[C/T]AGCGAGGCCTCAGCG | 1877 |
rs543875333 | snp | C/T | 0.000266068 | 0.011531 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232898 | TGTCAGCAAAGAGGA[C/T]GCACGTGCAGGTCAG | 1877 |
rs543919639 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222047 | CAACATGGTGAAACT[C/T]CGTCTCTCCTAAAAA | 1877 |
rs543978808 | snp | C/T | 1.77184e-05 | 0.00297639 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235203 | CCGCTCTTGCTGAGC[C/T]GTGGCCCTGCAGGTG | 1877 |
rs544001737 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223549 | CCCTCACGCTGGCCT[C/G/T]GGCGCGGCCCGTTGT | 1877 |
rs544741282 | in-del | -/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227827 | AATGTTTTAAAAACT[-/T]TTTTTTTTTTTTTTT | 1877 |
rs544779797 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223003 | CTCCAGCCTGGGCGA[C/T]AGAAAGAGACTCCGT | 1877 |
rs544810298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2229283 | CCTGCCAGAGTTGCT[A/G]CTCCCTCCCTGCAGG | 1877 |
rs544822081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2228887 | CTAGGGACTTCACAC[A/G]TGAAGTGTGGCCCTG | 1877 |
rs544883555 | snp | C/G/T | 0.0001562 | 0.00883627 | missense, synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233893 | CCAGCAGGTGGCCAG[C/G/T]GAGGCCTCAGCGGTG | 1877 |
rs545002319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230324 | GATGGGCAGGCTCTC[A/G]TCGGGGACAGATGCT | 1877 |
rs545063260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229828 | TTCTGCGGGCACAGC[C/T]TGCAGGAGGAGGAAG | 1877 |
rs545228886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226552 | TTTGCCCAGCTCCTT[C/T]GGGCATCAGGCCTGG | 1877 |
rs545292189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2231865 | TCACCAGGATTCGCA[C/T]GTCCTCCTGGCTTTG | 1877 |
rs545385916 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222084 | AAAATTAGCCGGGTG[C/T]GGTGGCAGTTGCCTG | 1877 |
rs545548940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2233393 | TGGGGTGGGTGCTGG[A/T]TGCCAGGCTGCCTGG | 1877 |
rs545657039 | snp | C/T | 0.000215169 | 0.0103701 | intron-variant | E4F1 | GRCh38.p7 | 16:2233674 | CACCACCTGCGGGCT[C/T]CTCCCAGGGCTGGAT | 1877 |
rs545712149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225755 | GGGAATACAGTCGTG[C/T]GCCACCGTGCCCGGC | 1877 |
rs545721478 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222786 | CCAGCACTTTGGGAG[A/G]CCGAGGCGGGCGGAT | 1877 |
rs546090889 | snp | G/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222879 | TACAAAAAATTAGCC[G/T]GGCGTGGTGGCGGAC | 1877 |
rs546127483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2224539 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGT | 1877 |
rs546435455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2223966 | CCTCTCCTGCGGGGC[C/G]CCTGTCATCCCCCCT | 1877 |
rs546597815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234842 | TTGCCTAGCCCTGAC[C/T]GAGTCCCCACCCACA | 1877 |
rs546817911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229894 | GGCCGGGGGCACACC[C/T]AGGCACCAGGGAGTC | 1877 |
rs547092769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2233284 | TCTGAGCCAGGCAGG[C/T]GAGGGCTGGGCTTCC | 1877 |
rs547108944 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231582 | TTGCACATTGTCAGA[C/T]TTTTCCCAGCATCCT | 1877 |
rs547365145 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | E4F1 | GRCh38.p7 | 16:2229390 | GGATTGGACTGGGAC[C/T]GGTGGTCGTGTTGGG | 1877 |
rs547398500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226615 | GTCAGAGCTGGCAGG[C/T]TTTTATGGAAGCAGA | 1877 |
rs547548045 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225663 | TTTTAGTAGAGACTG[C/G]ATTTCTCCATGTTGG | 1877 |
rs548007057 | snp | G/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223372 | CCCCCTGGCTGGCAA[G/T]CTGCTCCACCGTAAC | 1877 |
rs548196162 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226458 | CCATCAGGAGAGGAC[A/G]ACTCTGTTGGGTGGC | 1877 |
rs548400100 | snp | A/G | 0.00373531 | 0.0430547 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233630 | CTGCCGGTACTGGAA[A/G]TGCAGCCGCTGGAGA | 1877 |
rs548678614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229967 | TGCCGTGTCCCTCCC[A/G]GAATCTTCCCCACTT | 1877 |
rs548701625 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223102 | GAGCCATCCCCGACC[C/T]GTGTTCTTTTCCCGT | 1877 |
rs548826122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2227410 | GGAGTCTCGCTCTTT[C/T]GCCCAGGCTGGAGTG | 1877 |
rs549051976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234965 | GTTGGTGGAGTTCTC[A/G]TCCGTGGTAGCTGAC | 1877 |
rs549167809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2229006 | ACACGCCGCAGCGGG[C/T]GCTTGTCATCCGCAT | 1877 |
rs549208955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2225394 | ACCCCAACACTTTGG[A/G]AGGCTGAGGTGAGAG | 1877 |
rs549376301 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228748 | TTGGCAGCCTCTGGT[C/T]GAAGCCCGTGCTGTT | 1877 |
rs549478822 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2228584 | AGGTGGGGGAGGTGG[C/G]CGCGCTTCAGGATGG | 1877 |
rs549813797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226684 | CCCTGACACTCAGCC[A/G]TTTGGTGACCTTGAA | 1877 |
rs549818352 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223522 | GTTCTGCCCCGCCCT[C/T]CTCTTGCCGTTCCCT | 1877 |
rs549869922 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231762 | AAGAGTGGCCCCGGA[C/T]GCACATCCTCCCTAT | 1877 |
rs549906446 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | E4F1 | GRCh38.p7 | 16:2234079 | GGGTGGGTCCATAGA[C/T]AGCAGGGAGCCAGGG | 1877 |
rs549939621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231972 | TGACAGAGTCGGGAG[C/G]TGTCTCTCCACCTCT | 1877 |
rs550016838 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236036 | TCTGGGAGCCTCGGC[C/T]TCCACCGCAGGGTGA | 1877 |
rs550028886 | snp | C/G | | | intron-variant, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223808 | TGCGGCCGGGGTGCG[C/G]GCAGTTCATCCCGGG | 1877 |
rs550065657 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | E4F1 | GRCh38.p7 | 16:2225851 | CTGTAATCCCAGCAC[A/T]TTGGGAGGCTGAGAC | 1877 |
rs550403405 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234774 | GAACCGGCACCTGCG[C/T]ACCAAAGGTCTGGGC | 1877 |
rs550405043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229081 | GGCCACCAGTGGGCC[A/G]TGGCCCAGATGATGC | 1877 |
rs550896014 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222283 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCG | 1877 |
rs550928091 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2228039 | CCTCCCAGCCCCTCT[A/C]TGGGCCTCTCGCCTG | 1877 |
rs551031835 | snp | A/C/G | 0.000107913 | 0.00734478 | intron-variant | E4F1 | GRCh38.p7 | 16:2233195 | AGAGGTGGGGGCGAC[A/C/G]GGGGGCCCCGGAGGG | 1877 |
rs551204352 | snp | C/T | 0.000482302 | 0.0155215 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235324 | GAGACGGCGCTGGGC[C/T]CAGAGGCGGCTGCCG | 1877 |
rs551377487 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | E4F1 | GRCh38.p7 | 16:2231184 | GGCCAAGGGCTGGGG[C/T]GTGCCAGGTCCTGTC | 1877 |
rs551377575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2225559 | GCTCACCGCAACCTC[C/T]GCCTCCCGGGTTCAA | 1877 |
rs551551480 | snp | G/T | 0.000124836 | 0.00789952 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223807 | GTGCGGCCGGGGTGC[G/T]GGCAGTTCATCCCGG | 1877 |
rs551891208 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221537 | TAGCTAGGATTACAC[A/G]CGTGCACCACCACAC | 1877 |
rs552331332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227179 | CTACAGGTGCATGCC[A/G]CCACACTTCCACGCT | 1877 |
rs552394617 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | E4F1 | GRCh38.p7 | 16:2232694 | CCCCTGCCTGCCTTC[A/G]CCTTGTCACCTTGTC | 1877 |
rs552396437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2226753 | ATTTCCACAGGGTGC[C/T]GGCAAGATTTGGTGA | 1877 |
rs552806071 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223462 | CCCTTTAAGGCCACA[C/T]CGCTATCCAGGCCCG | 1877 |
rs552871906 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222799 | AGGCCGAGGCGGGCG[A/G]ATCACGAGGTCAGGA | 1877 |
rs552965184 | snp | C/T | 1.75807e-05 | 0.0029648 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234180 | CTGCAGGGCCGAGGC[C/T]GTTCGCCTGCGCGCA | 1877 |
rs553545176 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226715 | CTTCAGGTCATTTTC[C/T]TAGGATGGGAATAGT | 1877 |
rs553821423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2225877 | GAGACGGGCGGATCC[C/T]GAGGTCAGGAGATCG | 1877 |
rs553862865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225614 | GAGTAGCTGGGATTA[C/T]GGCACGCGGCATCAC | 1877 |
rs553931948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225078 | ATTAGCTGGGCGTGG[C/T]GGTGCGCGTCTGTAA | 1877 |
rs553953216 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224385 | CTGCCAGTAATGTAA[C/G]AAGCCCTTATCCTGC | 1877 |
rs554133139 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224186 | GGCCTCGGTTTCTCC[A/G]GGATCTGGGCTCTGG | 1877 |
rs554167134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229767 | TATGCTCGTCTCTCC[C/T]GAGACCAGGGCCTGG | 1877 |
rs554382647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2230199 | GATTGCTACACTGGT[C/T]CTCATGGGGCTTTTA | 1877 |
rs554413751 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229555 | GACTCCCCTGTTTTC[C/T]TCCCCCTTTGGCAGG | 1877 |
rs554506593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228177 | CTGGCCCCTGCAGAC[C/T]TGCAGAGGATAGGGG | 1877 |
rs554520634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2233326 | CAGGGCCAGTGGGAG[C/T]GCCATGGGGGTCTGA | 1877 |
rs554801748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227585 | CACGGTGTTAGCCAG[G/T]ATGGTCTCAATCTCC | 1877 |
rs554879081 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | E4F1 | GRCh38.p7 | 16:2231504 | CTAAGCAGTGGCTTC[A/C]CAGCTGTTTCCCACT | 1877 |
rs554915155 | snp | C/T | 0.000266735 | 0.0115454 | intron-variant | E4F1 | GRCh38.p7 | 16:2232441 | GGCCCTGAGCTGCCA[C/T]GCCCTCCCCCACAGG | 1877 |
rs554985849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226847 | GCACAGCAATGGTGA[C/T]GGGCTCAACCTTGGG | 1877 |
rs555106916 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223510 | CAATCCGCTCCGGTT[C/G]TGCCCCGCCCTCCTC | 1877 |
rs555109925 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236160 | GGCAGAGTCTAGGCG[A/C]CCTAATTTCTAGGGG | 1877 |
rs555119381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229216 | CTCACACCGCTCTGC[C/T]GGATGTGGCGGGCTG | 1877 |
rs555318087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224038 | CCGGGCGCCCGGTGT[A/G]GACATTCGCAGACGC | 1877 |
rs555333337 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230068 | CCACTCGCCCAGCAG[C/T]GGCTCTGGAGGGTGG | 1877 |
rs555859013 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222627 | GCACTTTGGGAGGCC[A/G]AAATGGGAAAATGGT | 1877 |
rs556381523 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227411 | GAGTCTCGCTCTTTC[A/G]CCCAGGCTGGAGTGC | 1877 |
rs556467331 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2230784 | TCATCAATGCCACTC[-/AG]AGCTCGGAATGTTCA | 1877 |
rs556531199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225167 | GCAGTAAGCCGAGAT[C/T]GCACCACTGCTCTCC | 1877 |
rs556568778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2233363 | GCACAAGGCTCCTGG[C/T]GTGCGTCTGCCCCAT | 1877 |
rs556768542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230837 | TGGCCTTGACCTGGC[A/G]TTTGGTTTCTGGGAT | 1877 |
rs556792905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228657 | GCAGGCACCTGGCTG[C/T]GGTGTGGGAGGGTCC | 1877 |
rs557380600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226932 | TTTGCCTCTCAGCCA[C/G]AGCCAGTGGGCATCA | 1877 |
rs557523344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224235 | AGCAGAGCCTAGTGC[A/C]AGAGGGCTGGTGCAC | 1877 |
rs557778178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224816 | CAGGGTCACCCAGGT[A/G]GTTAAGTAGCAAGGG | 1877 |
rs557840914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230108 | GGACGGGACTCTCCC[A/G]CCTCTCTAGCTGGGC | 1877 |
rs558124807 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230430 | CGGCAGGGGCGAGTG[A/G]CTAGGTGTGCAGACG | 1877 |
rs558160581 | snp | C/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221709 | CACAATTTTTTAAAA[C/G]TATGTAAGAGGGCTG | 1877 |
rs558422719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2229288 | CAGAGTTGCTGCTCC[C/T]TCCCTGCAGGCGCCC | 1877 |
rs558486175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234445 | TCCTGCTCCCTGGCC[A/G]TGGCCCAGGTGCACC | 1877 |
rs558562765 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | E4F1 | GRCh38.p7 | 16:2230979 | CTAGGCTCAGCACCC[C/G]TCCCTGTGCTTCAGC | 1877 |
rs558716972 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236108 | GCTGGTCCTACCTGC[C/G]CTGCCTTGCTTTCCC | 1877 |
rs558784921 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | E4F1 | GRCh38.p7 | 16:2226223 | CCTTGCCCCTTCTCG[C/T]TCCAGCTTGGAGAAG | 1877 |
rs558842274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225761 | ACAGTCGTGCGCCAC[C/T]GTGCCCGGCTCCTCC | 1877 |
rs558844494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231407 | AGGAGAGGCTCTTAA[C/T]TGTTTCTGAGTCACC | 1877 |
rs558958688 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222090 | AGCCGGGTGTGGTGG[C/T]AGTTGCCTGTAGTCC | 1877 |
rs559005242 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235784 | CTCCGCGGCTGGTGC[C/T]ACCACCTTTGCCCAG | 1877 |
rs559020263 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221547 | TACACGCGTGCACCA[C/T]CACACCCAGATAATT | 1877 |
rs559034112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227766 | TCAGCCTCCCAAAGT[A/G]TTGGGATTACAGGTG | 1877 |
rs559838826 | in-del | -/AA | 0.00557542 | 0.0525036 | intron-variant | E4F1 | GRCh38.p7 | 16:2231462 | ACAGCTTGTCAAAAC[-/AA]GACGCCAGCCGGACT | 1877 |
rs560322571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230435 | GGGGCGAGTGGCTAG[C/G]TGTGCAGACGCGAGG | 1877 |
rs560483622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2228988 | CAGGCCTGTGAACCC[C/T]GCACACGCCGCAGCG | 1877 |
rs560766438 | snp | C/T | 2.64253e-05 | 0.00363483 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223699 | AAGCGGGCGAGGGTG[C/T]AGTTGCGGCGGTGGC | 1877 |
rs560849176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229351 | TGTGAGAGTGACGGC[A/G]CTGACCCTGGCCCGG | 1877 |
rs561026899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231962 | CTGGGCAGCCTGACA[C/G]AGTCGGGAGGTGTCT | 1877 |
rs561042459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227023 | ACGCTCAAACTCCCG[C/T]AGTTTTTGTTTGTTT | 1877 |
rs561775570 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222915 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 1877 |
rs561834662 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | E4F1 | GRCh38.p7 | 16:2228826 | TCTGGGGTACCATGG[A/C]AGCTTCTGTCTCTTT | 1877 |
rs561921813 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225435 | GCCCAAGGAGTTCCA[A/G]ACCAGCCTGGGCAAC | 1877 |
rs562171322 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228468 | AGGCCTGCCAGCGGG[C/G]CCCTCCGGAGGCCCT | 1877 |
rs562394148 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | E4F1 | GRCh38.p7 | 16:2224632 | CTCTACTAAAAATAC[-/A]AAAAAAACAAAATTA | 1877 |
rs562722356 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224660 | TTAGCCGGGCGTGGT[A/G]GCGGGCGCCTGTAGT | 1877 |
rs562762677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231095 | CCAGTCAGCAGGCCC[A/G]GTGGGCTTAGTCCAG | 1877 |
rs562771864 | snp | G/T | 0.00808231 | 0.0630542 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223794 | GCCGACCCGGAGGGT[G/T]CGGCCGGGGTGCGGG | 1877 |
rs562834928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229389 | GGGATTGGACTGGGA[C/T]CGGTGGTCGTGTTGG | 1877 |
rs562884319 | snp | C/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223013 | GGCGATAGAAAGAGA[C/G]TCCGTCTCAAAAAAG | 1877 |
rs562930418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229779 | TCCCGAGACCAGGGC[C/G]TGGCTGGGAGGGGCC | 1877 |
rs563392255 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2227077 | GCAGGGTCTTGCCCT[G/T]TTGCCCTGGCTGAAG | 1877 |
rs563495207 | snp | G/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226231 | CTTCTCGTTCCAGCT[G/T]GGAGAAGGGCAGTGC | 1877 |
rs563650627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226484 | GTGGCCCCTGCAGGC[A/G]AGTCATAGCTGTGGT | 1877 |
rs564088935 | snp | A/C | | | intron-variant | E4F1 | GRCh38.p7 | 16:2233692 | CCCAGGGCTGGATCC[A/C]AGGGGCTGTCCCCAC | 1877 |
rs564228065 | snp | A/G | 2.12407e-05 | 0.00325882 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223625 | CGACATGGAGGGCGC[A/G]ATGGCAGTGCGGGTG | 1877 |
rs564377166 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | E4F1 | GRCh38.p7 | 16:2228111 | GTCCCTGCAGCCTAA[A/G]CGTGCTGTCAGGGCC | 1877 |
rs564556685 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223050 | AAAAAAATTAAAAGT[A/G]TATAAAAGAATAAAA | 1877 |
rs564766796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228902 | GTGAAGTGTGGCCCT[A/G]GGGGGTCCCGCCATC | 1877 |
rs564776934 | snp | A/C | 6.87226e-05 | 0.00586145 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228499 | GCCTGCCACCCCTGC[A/C]ACCACAGCGTTGCTG | 1877 |
rs564887396 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224456 | TGTTATTGTTATTCT[C/T]ATTTTGGGGATGAGG | 1877 |
rs564942581 | snp | C/T | 0.00546932 | 0.0520072 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234585 | GGTGTCTCCACAGAA[C/T]GCACAGCAGGTGCAC | 1877 |
rs564972673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225333 | GTACCCTCTGAGCTT[C/G]TCCTATGAGGCTGCA | 1877 |
rs564979481 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235953 | CCTGCCCAGCTGGAG[C/G]TGTGCCCCCAGCTGC | 1877 |
rs565109546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226966 | TCCTGGGCCCCAGCC[C/T]ATTTTACAGATGAGG | 1877 |
rs565177160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226566 | TCGGGCATCAGGCCT[A/G]GGTTTGATCCTGCCG | 1877 |
rs565189658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231871 | GGATTCGCACGTCCT[C/T]CTGGCTTTGGGGATG | 1877 |
rs565242919 | snp | C/T | 1.73782e-05 | 0.00294767 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235439 | TGCTTGCCGCCCGGG[C/T]AGGGACAAGTGGCAC | 1877 |
rs565702323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2233314 | CCACAGGGAGAGCAG[A/G]GCCAGTGGGAGCGCC | 1877 |
rs565876455 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2231994 | TCCACCTCTCACTCT[C/G]ACCTGGAGAGGTGAA | 1877 |
rs566143926 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236130 | TGCTTTCCCTGAAGG[C/G]ATTCTGCTCAGGGAG | 1877 |
rs566292104 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | E4F1 | GRCh38.p7 | 16:2232040 | TGCTCGGACCTGTGT[G/T]TTGAGGGCTCAGTGC | 1877 |
rs566348970 | snp | C/T | 0.000101363 | 0.00711838 | intron-variant | E4F1 | GRCh38.p7 | 16:2232730 | CCTGCTGGGGCTGCC[C/T]GGGGCTGACTAGGTT | 1877 |
rs566420745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2223978 | GGCGCCTGTCATCCC[C/G]CCTCTCTGGTGTGCG | 1877 |
rs566426803 | snp | A/C | 0.000874604 | 0.0208935 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234919 | GCCCCGCGGCAGCCA[A/C]CACCGTCCTCACGGA | 1877 |
rs566643474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2229897 | CGGGGGCACACCCAG[A/G]CACCAGGGAGTCATT | 1877 |
rs566897811 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222623 | CCTAGCACTTTGGGA[A/G]GCCGAAATGGGAAAA | 1877 |
rs566973067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228124 | AAGCGTGCTGTCAGG[G/T]CCACCCTCTGCTGGG | 1877 |
rs567182050 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223100 | ATGAGCCATCCCCGA[C/T]CCGTGTTCTTTTCCC | 1877 |
rs567239912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226096 | AGACTCCGCCTTGAA[A/G]GAAAAAAAAAAAAGA | 1877 |
rs567250531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231270 | CCCTCCTGCCGCTTC[A/G]CGGAAAAAGTTCGCG | 1877 |
rs567487667 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236007 | TGGGAGGACCAGGGA[C/T]GGGGACAGGGAGATC | 1877 |
rs567543806 | snp | A/C | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222181 | GAACCAAGATCGTGC[A/C]GTTGCATTCTAGCCT | 1877 |
rs567600771 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235688 | GAGGCGCCCCAAGAC[A/G]GACAGTGTACATAAG | 1877 |
rs567815872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230777 | AAGACACTCATCAAT[A/G]CCACTCAGAGCTCGG | 1877 |
rs567882180 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2234055 | GGCCGGGGTGCTTCT[G/T]GGTGTCCAGGGTGGG | 1877 |
rs567934857 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226503 | CATAGCTGTGGTTTG[A/G]CCCTTTCTCCGCCCT | 1877 |
rs568055470 | snp | G/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229368 | TGACCCTGGCCCGGG[G/T]GTGAAGGGATTGGAC | 1877 |
rs568128325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228587 | TGGGGGAGGTGGCCG[A/C]GCTTCAGGATGGACC | 1877 |
rs568471360 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228626 | CGGTTCCGGGGGCCA[C/T]GTGGGCGGGCAGAGG | 1877 |
rs568521071 | snp | C/T | 1.70043e-05 | 0.0029158 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232210 | TCGTGGCTGCTGAGG[C/T]GGAGCTGGGAGACGG | 1877 |
rs568522901 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2223992 | CCCCTCTCTGGTGTG[C/G]GTCCACAAGTGCTCG | 1877 |
rs568584625 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223293 | CGCCAGTCCGCTCGC[C/T]CCTCGCGTTCTCTGG | 1877 |
rs568666125 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | E4F1 | GRCh38.p7 | 16:2227441 | CAGTGGTGTGATCTC[A/G]GCTCACTGCAAGCTC | 1877 |
rs568841564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229970 | CGTGTCCCTCCCAGA[A/G]TCTTCCCCACTTCCC | 1877 |
rs569050435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225409 | GAGGCTGAGGTGAGA[C/G]GATCACTTGAGCCCA | 1877 |
rs569328828 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223279 | GGCTGCCTAGCAGCC[A/G]CCAGTCCGCTCGCCC | 1877 |
rs569337480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229017 | CGGGCGCTTGTCATC[C/T]GCATTGCACGGTCAG | 1877 |
rs569672809 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235772 | GGCAGTGGCAGCCTC[C/T]GCGGCTGGTGCCACC | 1877 |
rs569841751 | snp | A/G/T | 0.000133957 | 0.00818304 | intron-variant | E4F1 | GRCh38.p7 | 16:2229697 | CGACTTCCATGAATC[A/G/T]CTGGCCTGATAGACC | 1877 |
rs569878678 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231810 | CAGGAGCAGTGGCAG[C/T]GAGCAGGACAGGCGG | 1877 |
rs569998442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231391 | GTGTAAGGGCTCGGG[C/G]AGGAGAGGCTCTTAA | 1877 |
rs570063150 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236055 | ACCGCAGGGTGAGCA[A/G]GTGGAGCAGCAGCAG | 1877 |
rs570075736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2233731 | TCGCCTCCCTGAAGT[A/G]GCTTTCTGCAGTGAC | 1877 |
rs570201178 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2226166 | TGGGTTGAGGGTGGT[A/C]TTGTCTTTGTCCCCA | 1877 |
rs570282079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229474 | CACCACAAGTCACAC[C/T]TCCACAGCTTTACAC | 1877 |
rs570400416 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2229123 | CACCCCACTCTGAGC[A/C]TGTGCTCTTTACCTG | 1877 |
rs570462130 | snp | C/T | 0.000160891 | 0.00896771 | intron-variant | E4F1 | GRCh38.p7 | 16:2234130 | GCGGCCTGGCGGGCC[C/T]GCGGGTGATGGGCTT | 1877 |
rs570527683 | snp | G/T | 0 | 0 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223348 | AACATAGGTCCTTCT[G/T]CCGCCCCGCCCCCTG | 1877 |
rs570599480 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229398 | CTGGGACCGGTGGTC[A/G]TGTTGGGGAAGAGGA | 1877 |
rs570828769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2228050 | CTCTCTGGGCCTCTC[A/G]CCTGTCAGTCGCTGA | 1877 |
rs570937518 | snp | C/T | 0.00114694 | 0.0239198 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223786 | GTAACCGGGCCGACC[C/T]GGAGGGTGCGGCCGG | 1877 |
rs570940715 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | E4F1 | GRCh38.p7 | 16:2227496 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 1877 |
rs570940739 | snp | A/C/G | 0.000164583 | 0.00907016 | intron-variant | E4F1 | GRCh38.p7 | 16:2233205 | GCGACGGGGGGCCCC[A/C/G]GAGGGCTGCTCTGTC | 1877 |
rs571067152 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221737 | CTGAGGCAGGCAGAT[A/C]GCTTGAACTCAGGAG | 1877 |
rs571193329 | snp | C/T | 0.000403059 | 0.0141904 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223630 | TGGAGGGCGCGATGG[C/T]AGTGCGGGTGACGGC | 1877 |
rs571303896 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235677 | GGCACAGGATGGAGG[C/T]GCCCCAAGACGGACA | 1877 |
rs571352060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2230644 | GAGGGGGTGGAGGAG[C/T]CGTGGCGGAGGCCAA | 1877 |
rs571352122 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | E4F1 | GRCh38.p7 | 16:2224848 | TGGATTGGATCTCAG[C/T]ACTGTGAAGGCCTTC | 1877 |
rs571576707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226048 | CAGTGAGCTGAGATC[A/G]CCCCACTGCACTCCA | 1877 |
rs571722138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223820 | GCGGGCAGTTCATCC[C/T]GGGCTGGCAGAGGCC | 1877 |
rs572185598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230996 | CCCTGTGCTTCAGCA[G/T]CCCCTCTTGGCACCC | 1877 |
rs572289248 | snp | C/G | 2.08601e-05 | 0.00322949 | intron-variant | E4F1 | GRCh38.p7 | 16:2232420 | CCCCTCCTGTTCCCC[C/G]AGGAGGGCCCTGAGC | 1877 |
rs572317980 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227692 | TTTTAGTAGAGATGG[A/G]ATTTCACCATATTGG | 1877 |
rs572346538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226996 | GAGATGGCCACTCAC[A/C]TGCTCCAGGGCACGC | 1877 |
rs572408189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2226267 | TGGCGAGGAGTCCCT[C/T]TAGAGGTTGCTGGGC | 1877 |
rs572487058 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235794 | GGTGCCACCACCTTT[A/G]CCCAGGCCCCCGCAG | 1877 |
rs572559260 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | E4F1 | GRCh38.p7 | 16:2226194 | CCATAGGATTCATAG[-/TC]TCTGCCTTTTTTCCT | 1877 |
rs572599764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2226105 | CTTGAAAGAAAAAAA[A/G]AAAAGATGCAGATTG | 1877 |
rs572803733 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223474 | ACACCGCTATCCAGG[C/G]CCGGCTCCCCGCCTG | 1877 |
rs572931274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2233824 | CCATGGTTGTGTTCT[C/T]GGTACTGCCAGGGCA | 1877 |
rs573362015 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221827 | GCTAGTGATGGGCAC[C/T]TGTAGTCCCAGCTAC | 1877 |
rs573733612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2231055 | CCCTTTGCGGGCATC[C/T]TGGGTACTCTGTGTG | 1877 |
rs573896911 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235848 | CCTAGACTCACGTGC[C/T]TGGCCGCCCCACCCA | 1877 |
rs574231509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2230225 | TTTTATGAGCGTGCA[A/G]TGCCAGGACTCTTTG | 1877 |
rs574295861 | snp | A/C/T | 0.000189724 | 0.00973797 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235365 | CACCATCGCCACCCC[A/C/T]GAGAGCCTGACAGAG | 1877 |
rs574318798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229768 | ATGCTCGTCTCTCCC[A/G]AGACCAGGGCCTGGC | 1877 |
rs574509932 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224274 | GCCTGTGGCCCCTTC[C/G]AGTCCCACACTTGCC | 1877 |
rs574542864 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221960 | CTCGGTGGCTCATGC[C/T]TGTCATCCCAGCACT | 1877 |
rs574745094 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226872 | CTTGGGAACCAGTAA[A/T]GTCCCAAGTCAGTGA | 1877 |
rs574817067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226409 | AAGGGGAAGAGGGTG[C/G]TGGGCACCTTAGAGC | 1877 |
rs574866341 | snp | C/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221724 | GTATGTAAGAGGGCT[C/G]AGGCAGGCAGATCGC | 1877 |
rs575101270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2224197 | CTCCAGGATCTGGGC[C/T]CTGGGCCTGTCCGTA | 1877 |
rs575343524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | E4F1 | GRCh38.p7 | 16:2229225 | CTCTGCCGGATGTGG[C/T]GGGCTGGGACTGTGC | 1877 |
rs576046901 | snp | A/G | 6.888e-05 | 0.00586816 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235395 | GCAGGTGGCCATGAC[A/G]CTGGCCTCGGCCATC | 1877 |
rs576148083 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | E4F1 | GRCh38.p7 | 16:2226538 | TTCAACAGTAAACAT[C/T]TGCCCAGCTCCTTCG | 1877 |
rs576266110 | snp | A/G | 0.000101554 | 0.00712507 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232275 | CAGGGGCTGGGGCTC[A/G]CAGGGGAGGGTGAGC | 1877 |
rs576345658 | snp | C/T | 0.00259759 | 0.0359451 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232506 | CAGCCGCAAGGACCA[C/T]GAGTGCAAGCTCTGT | 1877 |
rs576388989 | snp | A/C/T | 0.000403699 | 0.014202 | intron-variant, synonymous-codon, missense | E4F1 | GRCh38.p7 | 16:2228311 | GGAGGAAAAGCCAGA[A/C/T]GGAGCCCTGGCTGCC | 1877 |
rs576405584 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223529 | CCCGCCCTCCTCTTG[C/G]CGTTCCCTCACGCTG | 1877 |
rs576440819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2227519 | TGGGACTATAGGCAC[C/G]TGCCACCATGCCTGG | 1877 |
rs576565106 | snp | A/G | 1.66863e-05 | 0.0028884 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233048 | CTTGGGGACAGCCAC[A/G]TCATCGGTGACAGGC | 1877 |
rs576645711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2225711 | TCCCGACCTCAGGTG[A/G]TCTGCCCGCCTCAGC | 1877 |
rs576926034 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | E4F1 | GRCh38.p7 | 16:2224527 | GGGTGCGGTGGCTCA[C/G]GCCTGTAATCCCAGC | 1877 |
rs577051440 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222765 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 1877 |
rs577113610 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226960 | TCAGTCTCCTGGGCC[C/G]CAGCCCATTTTACAG | 1877 |
rs577113994 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222078 | TATAAAAAAATTAGC[C/T]GGGTGTGGTGGCAGT | 1877 |
rs577126270 | snp | A/G | 7.07614e-05 | 0.00594775 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235168 | AGGGCAGGCGGGGGC[A/G]GGGAGGCTCCCTGGC | 1877 |
rs577462697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2226941 | CAGCCAGAGCCAGTG[A/G]GCATCAGTCTCCTGG | 1877 |
rs577647755 | in-del | -/A | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226097 | ACTCCGCCTTGAAAG[-/A]AAAAAAAAAAAAGAT | 1877 |
rs577741405 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230662 | TGGCGGAGGCCAACC[C/T]GGGGCCTGGGAAGGG | 1877 |
rs578188535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | E4F1 | GRCh38.p7 | 16:2229741 | CCAGAGGATGGGGCC[C/T]CTGCTGCCTGTATGC | 1877 |
rs745315027 | snp | C/T | 3.46188e-05 | 0.00416032 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235124 | AGGCCACGGAGATCA[C/T]CGAGGGCACCCAGAC | 1877 |
rs745359999 | snp | A/C/G | 6.50031e-05 | 0.00570071 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235585 | TAGCATGAGGTCTGC[A/C/G]GGGTCCTGGCCGGGC | 1877 |
rs745375897 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234933 | ACCACCGTCCTCACG[A/G]AAGACCCGCACACAG | 1877 |
rs745517753 | snp | C/T | 1.69666e-05 | 0.00291256 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233157 | ATGCAGGAGCTGTCC[C/T]TGGGCATGAAAGCCC | 1877 |
rs745605757 | snp | C/T | 1.77373e-05 | 0.00297797 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234423 | ACCCTGGCGCCTGAT[C/T]CCCCCATCCTGCTCC | 1877 |
rs745605953 | snp | C/G | 0.00141703 | 0.0265802 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233063 | ATCATCGGTGACAGG[C/G]GAGCCTATAGAGACT | 1877 |
rs745661683 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224799 | AAAGAAAAGAAAATG[A/G]CCAGGGTCACCCAGG | 1877 |
rs745711025 | snp | C/T | 1.72665e-05 | 0.00293819 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235424 | TCAGCGAGGGCACTG[C/T]GCTTGCCGCCCGGGC | 1877 |
rs745770809 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225588 | AAGCTATTCTCCTGA[C/T]TCGGCCTCCTGAGTA | 1877 |
rs745771766 | snp | A/G/T | 6.91448e-05 | 0.00587948 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235357 | GACACCATCACCATC[A/G/T]CCACCCCCGAGAGCC | 1877 |
rs745803461 | snp | C/T | 1.69178e-05 | 0.00290837 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228388 | TGAGGACGATGTGCA[C/T]AGATGCGGCCGCTGC | 1877 |
rs745913566 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223073 | GAATAAAACAGCTTC[A/G]CAGAGCTACCCATGA | 1877 |
rs746000717 | snp | A/G | 0.000253904 | 0.0112644 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233597 | AGTCCCCAGCCCCTG[A/G]CAGTGGCAGCCCCGC | 1877 |
rs746018946 | snp | C/G | 2.12538e-05 | 0.00325982 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223635 | GGCGCGATGGCAGTG[C/G]GGGTGACGGCCGCTC | 1877 |
rs746078819 | snp | C/T | 1.68829e-05 | 0.00290537 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234929 | AGCCACCACCGTCCT[C/T]ACGGAAGACCCGCAC | 1877 |
rs746084073 | snp | A/T | 2.49753e-05 | 0.0035337 | utr-variant-5-prime, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223581 | ATGACGACATGGTCG[A/T]AAATCCGCCATCTTC | 1877 |
rs746117638 | in-del | -/C | 5.31684e-05 | 0.00515571 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234422 | ACCCTGGCGCCTGAT[-/C]CCCCCCATCCTGCTC | 1877 |
rs746170340 | snp | A/G | 1.65913e-05 | 0.00288017 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229642 | GAGGCGGCCTCTCTG[A/G]CAGCAGACATCAGCC | 1877 |
rs746234698 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228586 | GTGGGGGAGGTGGCC[A/G]CGCTTCAGGATGGAC | 1877 |
rs746372944 | snp | A/G | 3.32458e-05 | 0.00407698 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232890 | GACGTGGTTGTCAGC[A/G]AAGAGGACGCACGTG | 1877 |
rs746462506 | snp | A/G | 1.86562e-05 | 0.00305414 | intron-variant | E4F1 | GRCh38.p7 | 16:2234152 | GATGGGCTTGGCCTG[A/G]TGCTGTGTGTGGCTG | 1877 |
rs746486192 | snp | A/G | 6.13591e-05 | 0.00553857 | intron-variant, splice-acceptor-variant | E4F1 | GRCh38.p7 | 16:2228290 | GGGGGAATCTGTTCT[A/G]GGGCTGGAGGAAAAG | 1877 |
rs746533922 | snp | A/G | 1.76428e-05 | 0.00297003 | stop-gained, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235218 | CGTGGCCCTGCAGGT[A/G]GACAGCCACATCATG | 1877 |
rs746571873 | snp | C/G | 0.000162456 | 0.0090112 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223828 | TTCATCCCGGGCTGG[C/G]AGAGGCCCGGATGGC | 1877 |
rs746572305 | snp | A/G | 2.01379e-05 | 0.0031731 | intron-variant | E4F1 | GRCh38.p7 | 16:2232382 | GAGCCGGCGTGCGGG[A/G]AGCCAGTGTGTGGGT | 1877 |
rs746609306 | in-del | -/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223544 | CCGTTCCCTCACGCT[-/G]GCCTCGGCGCGGCCC | 1877 |
rs746655240 | snp | A/G | 3.4915e-05 | 0.00417807 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235149 | CCAGACAGAGGTGAG[A/G]GGTAGGGCAGGCGGG | 1877 |
rs746661970 | snp | A/G | 0.000104825 | 0.0072389 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232320 | CTACTGGTGAACAAG[A/G]ATGGCCGCTATGTGT | 1877 |
rs746759448 | snp | A/G | 4.60585e-05 | 0.00479866 | intron-variant | E4F1 | GRCh38.p7 | 16:2233395 | GGGTGGGTGCTGGAT[A/G]CCAGGCTGCCTGGCC | 1877 |
rs746821546 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222284 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCGT | 1877 |
rs746851555 | snp | A/G | 3.92241e-05 | 0.00442838 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234633 | GGAGAAGCCGCACGT[A/G]TGCCAGTTCTGCAGC | 1877 |
rs746895780 | snp | A/G | 6.7086e-05 | 0.00579124 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234540 | GGAGAGCTGTAGTCT[A/G]TTGTGGCCAAGGCCA | 1877 |
rs746918557 | snp | A/G | 1.91562e-05 | 0.00309479 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235497 | ATCAGAGGACATCGA[A/G]ATCCTGGAGCATGCA | 1877 |
rs746928089 | snp | C/T | 1.81082e-05 | 0.00300895 | intron-variant | E4F1 | GRCh38.p7 | 16:2228533 | CAGGAGGTGAGCCCT[C/T]ACCCACTCCCCCATC | 1877 |
rs747006590 | snp | A/G | 1.73342e-05 | 0.00294394 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235432 | GGCACTGTGCTTGCC[A/G]CCCGGGCAGGGACAA | 1877 |
rs747033101 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229502 | CACTGGCAGAGCCCA[C/G]GCCTCTTCTCTGAGA | 1877 |
rs747064418 | snp | C/T | 1.69611e-05 | 0.00291209 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228471 | CCTGCCAGCGGGCCC[C/T]TCCGGAGGCCCTGCC | 1877 |
rs747116239 | in-del | -/A | 0.000317209 | 0.0125898 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234803 | GCCGGTGGAGGTGGG[-/A]GGGGGAGGGGAGGGG | 1877 |
rs747217683 | snp | C/G | 4.99463e-05 | 0.00499707 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233894 | CAGCAGGTGGCCAGC[C/G]AGGCCTCAGCGGTGC | 1877 |
rs747307359 | snp | A/G | 0.000295029 | 0.012142 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233620 | AGCCCCGCAGCTGCC[A/G]GTACTGGAAGTGCAG | 1877 |
rs747387668 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227396 | GTTTTTTTTGAAACG[A/G]AGTCTCGCTCTTTCG | 1877 |
rs747510999 | snp | A/C/T | 3.69101e-05 | 0.0042958 | intron-variant | E4F1 | GRCh38.p7 | 16:2228541 | GAGCCCTCACCCACT[A/C/T]CCCCATCCCCTCCCG | 1877 |
rs747601217 | snp | C/T | 1.68414e-05 | 0.0029018 | intron-variant | E4F1 | GRCh38.p7 | 16:2232952 | CCTGGGGGCTGGCTG[C/T]GGACGCAGCCGCCAC | 1877 |
rs747632415 | snp | C/T | 1.67416e-05 | 0.00289318 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234303 | AGCTCTACAAGACCA[C/T]TGCCCATGTGCGTGG | 1877 |
rs747666310 | snp | C/T | 3.53064e-05 | 0.00420142 | intron-variant, synonymous-codon | E4F1 | GRCh38.p7 | 16:2228358 | AGGCCCTGCTGACAG[C/T]AGGCTCGTTGCAGAT | 1877 |
rs747733148 | snp | C/T | 5.22198e-05 | 0.00510952 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235293 | GATCATCGTGCAGAA[C/T]GTCACCATGGACGAG | 1877 |
rs747767152 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221882 | AGTGAGCTGAGATCA[C/T]GGCACTGCACTCCAG | 1877 |
rs747806181 | snp | A/G | 7.66019e-05 | 0.0061883 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228309 | CTGGAGGAAAAGCCA[A/G]ACGGAGCCCTGGCTG | 1877 |
rs747908249 | in-del | -/C | 7.64906e-05 | 0.00618381 | intron-variant | E4F1 | GRCh38.p7 | 16:2233876 | GACCTTCCTGTGGTT[-/C]CCCAGCAGGTGGCCA | 1877 |
rs747928080 | snp | G/T | | | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234453 | CCTGGCCGTGGCCCA[G/T]GTGCACCCCCTTCCC | 1877 |
rs747930778 | snp | C/G | 2.06776e-05 | 0.00321533 | intron-variant | E4F1 | GRCh38.p7 | 16:2232400 | CCAGTGTGTGGGTGG[C/G]AGGCCCCCTCCTGTT | 1877 |
rs747936086 | snp | C/T | 5.43149e-05 | 0.005211 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232339 | GCCGCTATGTGTGTG[C/T]GCTGTGCCACAAGAC | 1877 |
rs747998671 | in-del | -/C | 1.96273e-05 | 0.00313261 | intron-variant, frameshift-variant | E4F1 | GRCh38.p7 | 16:2228339 | CCCAGCCTCCGCCTT[-/C]CCCAGGCCCTGCTGA | 1877 |
rs748010768 | snp | A/C | 2.47767e-05 | 0.00351962 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233495 | CGTGAGAACCTGCTG[A/C]ACCAGGCCATGCAGA | 1877 |
rs748019819 | snp | C/T | 3.72849e-05 | 0.00431753 | intron-variant | E4F1 | GRCh38.p7 | 16:2233430 | TCCTCTCTCTGCCTC[C/T]CCTGCAGCCCCCCGT | 1877 |
rs748161592 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222182 | AACCAAGATCGTGCC[A/G]TTGCATTCTAGCCTA | 1877 |
rs748169224 | snp | C/T | 4.53155e-05 | 0.0047598 | stop-gained, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234658 | TGCAGCCGTGGCTTC[C/T]GAGAGAAGGGCTCAC | 1877 |
rs748182529 | snp | A/C | 1.66638e-05 | 0.00288645 | intron-variant | E4F1 | GRCh38.p7 | 16:2229554 | CGACTCCCCTGTTTT[A/C]TTCCCCCTTTGGCAG | 1877 |
rs748247093 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229978 | TCCCAGAATCTTCCC[C/T]ACTTCCCTGCCACCC | 1877 |
rs748279043 | snp | C/T | 9.96264e-05 | 0.00705714 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232865 | GAAAATCCGCTTCAG[C/T]GTGAGCAAGGACGTG | 1877 |
rs748293568 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230049 | AGGCACCCACCAGAA[C/T]GGCCCACTCGCCCAG | 1877 |
rs748369000 | snp | G/T | 3.35807e-05 | 0.00409747 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232757 | GGTTCTCTCTGCAGA[G/T]GAGCGCCCCTACAAG | 1877 |
rs748400100 | snp | C/T | 4.71109e-05 | 0.00485317 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233983 | GGCCCACAAGAGGGG[C/T]CACACCGGTAGGTGA | 1877 |
rs748490046 | snp | A/G | 8.64207e-05 | 0.00657289 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235098 | CACTGCGGACGATGC[A/G]GAGACCAGTGAGGCC | 1877 |
rs748540599 | snp | C/T | 8.97143e-05 | 0.00669695 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233904 | CCAGCGAGGCCTCAG[C/T]GGTGCCCAGGACCCA | 1877 |
rs748576332 | snp | C/G/T | 3.52206e-05 | 0.00419631 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223727 | GGCGGCGGCCTTGGC[C/G/T]CCCAGCGGCTTCCTC | 1877 |
rs748664813 | snp | C/T | 4.07805e-05 | 0.00451537 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235017 | GTGGGTGTGGGGCCC[C/T]GGGGCCGTGCTGGGA | 1877 |
rs748690987 | snp | C/G/T | 3.3694e-05 | 0.0041044 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232242 | GAGATGGCCGAGGCC[C/G/T]CGGGCAGCCCCCGCC | 1877 |
rs748694000 | snp | A/C | 1.71114e-05 | 0.00292496 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232185 | GGTGGTGGGCACATC[A/C]AAGAGGTCATCGTGG | 1877 |
rs748790884 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224884 | CCCTTTAACTTCCGG[A/G]CTCTGCTGCCTCATA | 1877 |
rs748906678 | snp | C/G | 1.68357e-05 | 0.00290131 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228455 | CACAAGATTCAGAAG[C/G]CCTGCCAGCGGGCCC | 1877 |
rs748928929 | snp | A/G | 1.67399e-05 | 0.00289304 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234313 | GACCATTGCCCATGT[A/G]CGTGGCCACCGGCGC | 1877 |
rs748984863 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226830 | TGCACGACCGGGGTC[C/T]GGCACAGCAATGGTG | 1877 |
rs749016844 | snp | C/G | 7.0028e-05 | 0.00591685 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235344 | GGCGGCTGCCGCCGA[C/G]ACCATCACCATCGCC | 1877 |
rs749054992 | snp | A/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225326 | TGGGTCTGTACCCTC[A/T]GAGCTTGTCCTATGA | 1877 |
rs749101506 | snp | A/G | 1.7402e-05 | 0.0029497 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235308 | CGTCACCATGGACGA[A/G]GAGACGGCGCTGGGC | 1877 |
rs749141504 | snp | A/G | 5.73839e-05 | 0.00535618 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232496 | TCACTCACAGCAGCC[A/G]CAAGGACCACGAGTG | 1877 |
rs749206599 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233509 | GCACCAGGCCATGCA[G/T]AACTCCGGCATCGTC | 1877 |
rs749230680 | snp | A/G | 6.25202e-05 | 0.00559072 | intron-variant | E4F1 | GRCh38.p7 | 16:2232413 | GGCAGGCCCCCTCCT[A/G]TTCCCCCAGGAGGGC | 1877 |
rs749236840 | snp | A/G | 1.74839e-05 | 0.00295663 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233582 | CCTGCTGCCGGGTCC[A/G]GTCCCCAGCCCCTGG | 1877 |
rs749272911 | snp | C/T | 0.000105994 | 0.00727913 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234923 | CGCGGCAGCCACCAC[C/T]GTCCTCACGGAAGAC | 1877 |
rs749334486 | snp | A/G | 2.56157e-05 | 0.00357872 | utr-variant-5-prime, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223568 | GCGGCCCGTTGTTAT[A/G]ACGACATGGTCGTAA | 1877 |
rs749451593 | snp | A/G | 5.67135e-05 | 0.0053248 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234676 | GAGAAGGGCTCACTG[A/G]TGCGGCACGTGCGAC | 1877 |
rs749481310 | snp | C/T | | | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234344 | GTCCACTCAGACGAG[C/T]GGCCCTACCCTTGTC | 1877 |
rs749515737 | snp | A/G | 4.98434e-05 | 0.00499192 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229578 | TTGGCAGGTGGTGCC[A/G]GCAGCACCAGGCCCA | 1877 |
rs749655806 | snp | G/T | 1.94865e-05 | 0.00312136 | intron-variant | E4F1 | GRCh38.p7 | 16:2234137 | GGCGGGCCCGCGGGT[G/T]ATGGGCTTGGCCTGA | 1877 |
rs749680829 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231117 | TTAGTCCAGGGCTGC[C/T]AGCTCTCCTGTTGGC | 1877 |
rs749705386 | snp | C/T | 1.67416e-05 | 0.00289318 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232769 | AGATGAGCGCCCCTA[C/T]AAGTGCTCCAAGTGT | 1877 |
rs749793321 | snp | A/G | 5.27858e-05 | 0.00513713 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233990 | AAGAGGGGCCACACC[A/G]GTAGGTGATGGGTGG | 1877 |
rs749804408 | snp | A/G | 1.77068e-05 | 0.00297541 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235201 | AGCCGCTCTTGCTGA[A/G]CCGTGGCCCTGCAGG | 1877 |
rs749813849 | snp | A/C | 0.000135181 | 0.00822023 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223815 | GGGGTGCGGGCAGTT[A/C]ATCCCGGGCTGGCAG | 1877 |
rs749988881 | snp | A/G | 7.47747e-05 | 0.00611406 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234711 | CACAGGCGAGAAGCC[A/G]TTCAAGTGCTACAAG | 1877 |
rs750073803 | snp | A/G/T | 0.0001978 | 0.00994311 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234627 | CCTGGAGGAGAAGCC[A/G/T]CACGTGTGCCAGTTC | 1877 |
rs750115247 | snp | A/G | 1.67066e-05 | 0.00289016 | intron-variant | E4F1 | GRCh38.p7 | 16:2229537 | ACTCTGGAGCATACA[A/G]ACGACTCCCCTGTTT | 1877 |
rs750129537 | in-del | -/G | 0 | 0 | intron-variant | E4F1 | GRCh38.p7 | 16:2233194 | AGAGGTGGGGGCGAC[-/G]GGGGGGCCCCGGAGG | 1877 |
rs750143067 | snp | C/T | 1.66065e-05 | 0.00288149 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232816 | AGTCGGGTGCACTGA[C/T]CCGGCACCTCAAGTC | 1877 |
rs750226059 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226579 | CTGGGTTTGATCCTG[C/T]CGAGGGACTGAAGGT | 1877 |
rs750233058 | snp | C/T | 2.08335e-05 | 0.00322744 | intron-variant | E4F1 | GRCh38.p7 | 16:2234124 | TGGCAGGCGGCCTGG[C/T]GGGCCCGCGGGTGAT | 1877 |
rs750279613 | snp | C/T | 1.69115e-05 | 0.00290782 | intron-variant | E4F1 | GRCh38.p7 | 16:2232719 | CTTGTCGCCAGCCTG[C/T]TGGGGCTGCCCGGGG | 1877 |
rs750373926 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228160 | ACCTCCTGAGGGTGG[A/G]TCTGGCCCCTGCAGA | 1877 |
rs750399846 | snp | G/T | 9.85367e-05 | 0.00701845 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223790 | CCGGGCCGACCCGGA[G/T]GGTGCGGCCGGGGTG | 1877 |
rs750461810 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222009 | CGGATCACCTGAGGT[C/T]AGGAGTTCAAAACCA | 1877 |
rs750479852 | snp | A/G | | | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234284 | CGCTGTGGCGACTGC[A/G]GGAAGCTCTACAAGA | 1877 |
rs750488930 | snp | G/T | 3.37901e-05 | 0.00411022 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232270 | GCCAGCAGGGGCTGG[G/T]GCTCGCAGGGGAGGG | 1877 |
rs750543799 | snp | A/G | 5.67006e-05 | 0.0053242 | intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234989 | AGCTGACACCCAGGA[A/G]TATATCATCGAGGTG | 1877 |
rs750664055 | snp | C/T | 5.04927e-05 | 0.00502432 | intron-variant | E4F1 | GRCh38.p7 | 16:2229707 | GAATCGCTGGCCTGA[C/T]AGACCTTCGTGGTTG | 1877 |
rs750675436 | snp | A/G | 1.6633e-05 | 0.00288378 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233106 | CACCTGGTGACAGAT[A/G]CCAAGGGCACCGTCA | 1877 |
rs750763458 | snp | C/T | 3.35345e-05 | 0.00409465 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234352 | AGACGAGCGGCCCTA[C/T]CCTTGTCCCAAGTGT | 1877 |
rs750767205 | snp | C/T | 0.00016709 | 0.00913877 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233030 | TGGAGCTGGAGCTGC[C/T]GGCTTGGGGACAGCC | 1877 |
rs750857483 | snp | C/T | 1.67478e-05 | 0.00289372 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234292 | CGACTGCGGGAAGCT[C/T]TACAAGACCATTGCC | 1877 |
rs750922254 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224404 | CCCTTATCCTGCTTT[A/G]GGTTTTTTCATTCTC | 1877 |
rs750945693 | snp | A/T | 1.7782e-05 | 0.00298173 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232552 | ACCAAGGGCTCACTC[A/T]TCCGGCACCACCGGC | 1877 |
rs750945798 | snp | C/T | 0.000129281 | 0.0080389 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228347 | TCCGCCTTCCCAGGC[C/T]CTGCTGACAGCAGGC | 1877 |
rs750966173 | snp | G/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230772 | CGACCAAGACACTCA[G/T]CAATGCCACTCAGAG | 1877 |
rs751032252 | snp | C/T | 2.01871e-05 | 0.00317697 | intron-variant | E4F1 | GRCh38.p7 | 16:2232450 | CTGCCACGCCCTCCC[C/T]CACAGGGCAGCATCC | 1877 |
rs751100321 | in-del | -/CCT | 4.30877e-05 | 0.00464133 | intron-variant | E4F1 | GRCh38.p7 | 16:2233413 | AGGCTGCCTGGCCAG[-/CCT]CCTCTCTCTGCCTCC | 1877 |
rs751126806 | snp | A/G | 5.56375e-05 | 0.00527405 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233543 | GAGCGCGCTGCTGGG[A/G]AGGAGGGTGCCCTGG | 1877 |
rs751216480 | snp | A/T | 0.000714439 | 0.0188867 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234846 | CTAGCCCTGACCGAG[A/T]CCCCACCCACAGGGG | 1877 |
rs751255718 | snp | A/G | 1.76294e-05 | 0.0029689 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234734 | GCTACAAGTGCGGCC[A/G]TGGCTTCGCCGAGCA | 1877 |
rs751372530 | snp | A/C/G | 4.99117e-05 | 0.00499537 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232903 | GCAAAGAGGACGCAC[A/C/G]TGCAGGTCAGCATGG | 1877 |
rs751433198 | snp | C/T | 1.66779e-05 | 0.00288768 | intron-variant | E4F1 | GRCh38.p7 | 16:2229547 | ATACAGACGACTCCC[C/T]TGTTTTCTTCCCCCT | 1877 |
rs751508046 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231742 | CAGCCCATCTCCTCC[A/G]ATGGAAGAGTGGCCC | 1877 |
rs751547314 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224566 | AGGTCGAGACGGGCG[A/G]GTCACGAGGTCAGGA | 1877 |
rs751586767 | snp | A/G | 2.02325e-05 | 0.00318054 | intron-variant | E4F1 | GRCh38.p7 | 16:2234127 | CAGGCGGCCTGGCGG[A/G]CCCGCGGGTGATGGG | 1877 |
rs751663604 | snp | C/G | 0.00018655 | 0.00965609 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223893 | AGACACCTCGCGGAT[C/G]TCGCGGGACCCTCAC | 1877 |
rs751674551 | snp | A/G | 4.21861e-05 | 0.00459252 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233965 | GACAGCAGCCACCCT[A/G]GAGGCCCACAAGAGG | 1877 |
rs751676637 | snp | C/G | 1.77297e-05 | 0.00297734 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235174 | GGCGGGGGCGGGGAG[C/G]CTCCCTGGCACAGCC | 1877 |
rs751753632 | snp | C/T | 3.97551e-05 | 0.00445825 | intron-variant, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223799 | CCCGGAGGGTGCGGC[C/T]GGGGTGCGGGCAGTT | 1877 |
rs751916028 | snp | C/G | 0.000199704 | 0.0099906 | intron-variant | E4F1 | GRCh38.p7 | 16:2233202 | GGGGCGACGGGGGGC[C/G]CCGGAGGGCTGCTCT | 1877 |
rs751937000 | snp | A/G | 5.05685e-05 | 0.00502809 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232236 | GACGGTGAGATGGCC[A/G]AGGCCCCGGGCAGCC | 1877 |
rs751992468 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221823 | ATTAGCTAGTGATGG[A/G]CACCTGTAGTCCCAG | 1877 |
rs752006264 | snp | A/G | 0.00010329 | 0.0071857 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234588 | GTCTCCACAGAACGC[A/G]CAGCAGGTGCACTTC | 1877 |
rs752025643 | snp | A/G | 3.44756e-05 | 0.0041517 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228503 | GCCACCCCTGCCACC[A/G]CAGCGTTGCTGGGCC | 1877 |
rs752143172 | snp | G/T | 1.72178e-05 | 0.00293404 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235402 | GCCATGACGCTGGCC[G/T]CGGCCATCAGCGAGG | 1877 |
rs752283262 | snp | C/T | 3.51568e-05 | 0.00419251 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235338 | CCCAGAGGCGGCTGC[C/T]GCCGACACCATCACC | 1877 |
rs752306108 | snp | C/T | 0.000141711 | 0.00841637 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232567 | ATCCGGCACCACCGG[C/T]GGCACACGGGTGAGC | 1877 |
rs752344146 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229299 | CTCCCTCCCTGCAGG[C/T]GCCCTGTGCTCCAGG | 1877 |
rs752392892 | snp | A/G | 0.00108831 | 0.0233017 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223685 | CGAAGCCGGGCGGGA[A/G]GCGGGCGAGGGTGCA | 1877 |
rs752492992 | snp | C/T | 0.000401544 | 0.0141637 | intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234968 | GGTGGAGTTCTCGTC[C/T]GTGGTAGCTGACACC | 1877 |
rs752495113 | snp | G/T | 1.72472e-05 | 0.00293654 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233573 | GAGCCAGCTCCTGCT[G/T]CCGGGTCCAGTCCCC | 1877 |
rs752553910 | snp | A/G | 1.66513e-05 | 0.00288537 | intron-variant | E4F1 | GRCh38.p7 | 16:2229678 | TCTGACCTTGTTGGT[A/G]AGCCGACTTCCATGA | 1877 |
rs752582808 | snp | A/C | 0.00011764 | 0.00766852 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234908 | GTCTGAGGACAGCCC[A/C]GCGGCAGCCACCACC | 1877 |
rs752641682 | snp | C/T | 1.65858e-05 | 0.00287969 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229620 | CACTGTGGCCCACAT[C/T]GTGGTGGAGGCGGCC | 1877 |
rs752646018 | snp | A/C | 3.34588e-05 | 0.00409002 | intron-variant | E4F1 | GRCh38.p7 | 16:2232985 | GGGTGTGTGAGGGAT[A/C]TTCACTCCCTCACTC | 1877 |
rs752735909 | snp | A/G | 1.66521e-05 | 0.00288544 | intron-variant | E4F1 | GRCh38.p7 | 16:2232913 | CGCACGTGCAGGTCA[A/G]CATGGTGCGGGCAGC | 1877 |
rs752795153 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226473 | GACTCTGTTGGGTGG[C/G]CCCTGCAGGCGAGTC | 1877 |
rs752817543 | snp | A/C | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223313 | GCGTTCTCTGGCTCT[A/C]AAATCCGAGTGCAGC | 1877 |
rs752962126 | snp | C/T | 0.000159942 | 0.00894123 | intron-variant | E4F1 | GRCh38.p7 | 16:2234132 | GGCCTGGCGGGCCCG[C/T]GGGTGATGGGCTTGG | 1877 |
rs752989811 | snp | C/G | 0.000198 | 0.00994791 | intron-variant | E4F1 | GRCh38.p7 | 16:2223943 | AGGTTTGCTGCGACC[C/G]TCACGGGCCTCTCCT | 1877 |
rs753059691 | snp | C/G | 0.000119663 | 0.00773416 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232298 | GGGTGAGCAGGCCCA[C/G]GTGAAGCTACTGGTG | 1877 |
rs753134859 | snp | A/G/T | 0.000189163 | 0.00972358 | intron-variant | E4F1 | GRCh38.p7 | 16:2233233 | GTCTTCTGCCTGCTC[A/G/T]GTGCCAGTCTTTGTT | 1877 |
rs753182356 | snp | C/T | | | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235076 | CCTTCTGCCCATCTG[C/T]CCAGGCCACTGCGGA | 1877 |
rs753257858 | snp | G/T | 2.18759e-05 | 0.00330718 | intron-variant | E4F1 | GRCh38.p7 | 16:2228573 | GTTCACCTGACAGGT[G/T]GGGGAGGTGGCCGCG | 1877 |
rs753386458 | snp | C/T | 1.79696e-05 | 0.00299741 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235475 | AGGCCACTGTGACCA[C/T]GGTGTCATCAGAGGA | 1877 |
rs753476220 | snp | A/C | 1.72326e-05 | 0.0029353 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235410 | GCTGGCCTCGGCCAT[A/C]AGCGAGGGCACTGTG | 1877 |
rs753559375 | snp | C/T | 1.69238e-05 | 0.00290888 | intron-variant | E4F1 | GRCh38.p7 | 16:2232709 | GCCTTGTCACCTTGT[C/T]GCCAGCCTGCTGGGG | 1877 |
rs753622918 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229105 | ATGATGCTGGACCCT[A/G]GACACCCCACTCTGA | 1877 |
rs753628444 | snp | C/T | 1.74467e-05 | 0.00295348 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235068 | ACCTCTGTCCTTCTG[C/T]CCATCTGCCCAGGCC | 1877 |
rs753644907 | snp | A/G | 1.76808e-05 | 0.00297323 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232575 | CCACCGGCGGCACAC[A/G]GGTGAGCTGGCCGCA | 1877 |
rs753648277 | snp | C/G | 3.85334e-05 | 0.00438922 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233943 | CTCAGTGCAGTGAGA[C/G]CTTCCCGACAGCAGC | 1877 |
rs753711774 | snp | C/T | 1.67668e-05 | 0.00289537 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228442 | GGATTTTGTTCAGCA[C/T]AAGATTCAGAAGGCC | 1877 |
rs753736178 | snp | C/G | 1.68069e-05 | 0.00289882 | intron-variant | E4F1 | GRCh38.p7 | 16:2233859 | CTGCCCCGGGTGCTG[C/G]AGACCTTCCTGTGGT | 1877 |
rs753813526 | snp | A/G | 1.65641e-05 | 0.00287781 | intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234974 | GTTCTCGTCCGTGGT[A/G]GCTGACACCCAGGAG | 1877 |
rs753827991 | snp | A/C/T | 8.48233e-05 | 0.00651194 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232216 | CTGCTGAGGCGGAGC[A/C/T]GGGAGACGGTGAGAT | 1877 |
rs753924202 | snp | A/G | 0.00011682 | 0.00764173 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233019 | CTTGAAGGTTCTGGA[A/G]CTGGAGCTGCCGGCT | 1877 |
rs754184318 | snp | C/T | 3.45316e-05 | 0.00415507 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234192 | GGCCGTTCGCCTGCG[C/T]GCAGTGTGGCAAGGC | 1877 |
rs754200639 | snp | C/T | 2.00102e-05 | 0.00316302 | intron-variant, synonymous-codon | E4F1 | GRCh38.p7 | 16:2228337 | CTGCCCAGCCTCCGC[C/T]TTCCCAGGCCCTGCT | 1877 |
rs754240768 | in-del | -/GGGTGT | 1.67534e-05 | 0.0028942 | intron-variant | E4F1 | GRCh38.p7 | 16:2232969 | ACGCAGCCGCCACTG[-/GGGTGT]GGGTGTGTGAGGGAT | 1877 |
rs754298020 | snp | C/G | 1.74668e-05 | 0.00295518 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235272 | CCAGGCTAGCGCCGG[C/G]CACCAGATCATCGTG | 1877 |
rs754421089 | snp | C/T | 1.77979e-05 | 0.00298306 | intron-variant, synonymous-codon | E4F1 | GRCh38.p7 | 16:2228355 | CCCAGGCCCTGCTGA[C/T]AGCAGGCTCGTTGCA | 1877 |
rs754551029 | snp | C/G | 7.22831e-05 | 0.00601135 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233552 | GCTGGGGAGGAGGGT[C/G]CCCTGGAGCCAGCTC | 1877 |
rs754597262 | snp | A/C | 2.021e-05 | 0.00317877 | intron-variant | E4F1 | GRCh38.p7 | 16:2232387 | GGCGTGCGGGGAGCC[A/C]GTGTGTGGGTGGCAG | 1877 |
rs754623104 | snp | C/G | 0.000138437 | 0.00831862 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228486 | CTCCGGAGGCCCTGC[C/G]TGCCACCCCTGCCAC | 1877 |
rs754715232 | snp | C/T | 2.46436e-05 | 0.00351016 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233492 | AGCCGTGAGAACCTG[C/T]TGCACCAGGCCATGC | 1877 |
rs754733023 | snp | C/T | 1.97799e-05 | 0.00314476 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234885 | CTGGAGGTGGAGGAG[C/T]TGCTGGTGTCTGAGG | 1877 |
rs754821128 | snp | A/G | 0.000106264 | 0.00728841 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234742 | TGCGGCCGTGGCTTC[A/G]CCGAGCACGGCACGC | 1877 |
rs754829654 | snp | C/T | 1.65853e-05 | 0.00287964 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229614 | GCCCATCACTGTGGC[C/T]CACATCGTGGTGGAG | 1877 |
rs754853164 | snp | C/T | 1.66782e-05 | 0.0028877 | intron-variant | E4F1 | GRCh38.p7 | 16:2229548 | TACAGACGACTCCCC[C/T]GTTTTCTTCCCCCTT | 1877 |
rs754933280 | in-del | -/CA | 4.19948e-05 | 0.0045821 | intron-variant | E4F1 | GRCh38.p7 | 16:2233416 | TGCCTGGCCAGCCTC[-/CA]CTCTCTCTGCCTCCC | 1877 |
rs755001971 | snp | C/T | 2.00813e-05 | 0.00316864 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235507 | ATCGAGATCCTGGAG[C/T]ATGCAGGCGAGCTGG | 1877 |
rs755060372 | snp | C/T | 1.68227e-05 | 0.00290018 | intron-variant | E4F1 | GRCh38.p7 | 16:2232748 | GGCTGACTAGGTTCT[C/T]TCTGCAGATGAGCGC | 1877 |
rs755148355 | snp | A/G | 8.61623e-05 | 0.00656306 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233969 | GCAGCCACCCTGGAG[A/G]CCCACAAGAGGGGCC | 1877 |
rs755186314 | snp | C/T | 3.55764e-05 | 0.00421746 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235180 | GGCGGGGAGGCTCCC[C/T]GGCACAGCCGCTCTT | 1877 |
rs755203704 | snp | A/G | 5.18704e-05 | 0.0050924 | synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235093 | CAGGCCACTGCGGAC[A/G]ATGCGGAGACCAGTG | 1877 |
rs755324797 | snp | C/G | 5.09775e-05 | 0.00504838 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232287 | CTCGCAGGGGAGGGT[C/G]AGCAGGCCCAGGTGA | 1877 |
rs755412650 | snp | C/T | 1.68516e-05 | 0.00290268 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232240 | GTGAGATGGCCGAGG[C/T]CCCGGGCAGCCCCCG | 1877 |
rs755569656 | snp | A/G | 5.20458e-05 | 0.005101 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234403 | GGTGGGTCTCTGGCC[A/G]CAGGACCCTGGCGCC | 1877 |
rs755582316 | snp | C/T | 1.67388e-05 | 0.00289294 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234310 | CAAGACCATTGCCCA[C/T]GTGCGTGGCCACCGG | 1877 |
rs755607071 | snp | A/G/T | 3.35916e-05 | 0.00409815 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228450 | TTCAGCACAAGATTC[A/G/T]GAAGGCCTGCCAGCG | 1877 |
rs755627850 | snp | C/T | 1.72311e-05 | 0.00293518 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235403 | CCATGACGCTGGCCT[C/T]GGCCATCAGCGAGGG | 1877 |
rs755635964 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227785 | GGATTACAGGTGTGA[A/G]CCACCACACCCAGCC | 1877 |
rs755691762 | in-del | -/CT | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231984 | GAGGTGTCTCTCCAC[-/CT]CTCACTCTGACCTGG | 1877 |
rs755698323 | snp | A/G | 1.76702e-05 | 0.00297234 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232571 | GGCACCACCGGCGGC[A/G]CACGGGTGAGCTGGC | 1877 |
rs755713708 | snp | A/G | 3.51457e-05 | 0.00419185 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235339 | CCAGAGGCGGCTGCC[A/G]CCGACACCATCACCA | 1877 |
rs755724364 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224833 | TTAAGTAGCAAGGGT[C/T]GGATTGGATCTCAGC | 1877 |
rs755758908 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225136 | GAGAATTGCTTGAGC[C/T]CAGGAGACGGAGGTC | 1877 |
rs755767387 | snp | C/T | 0.000122035 | 0.00781042 | intron-variant, synonymous-codon | E4F1 | GRCh38.p7 | 16:2228364 | TGCTGACAGCAGGCT[C/T]GTTGCAGATGAGGAC | 1877 |
rs755899887 | snp | A/G | 0.000553986 | 0.0166339 | intron-variant | E4F1 | GRCh38.p7 | 16:2233851 | GGCACAGCCTGCCCC[A/G]GGTGCTGGAGACCTT | 1877 |
rs755934998 | in-del | -/G | 3.49871e-05 | 0.00418238 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234413 | TGGCCGCAGGACCCT[-/G]GCGCCTGATCCCCCC | 1877 |
rs755989987 | snp | C/T | 0.00161812 | 0.0283979 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233575 | GCCAGCTCCTGCTGC[C/T]GGGTCCAGTCCCCAG | 1877 |
rs755991498 | snp | G/T | 1.66214e-05 | 0.00288278 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223563 | TCGGCGCGGCCCGTT[G/T]TTATGACGACATGGT | 1877 |
rs756118944 | snp | A/G | 3.31724e-05 | 0.00407248 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229621 | ACTGTGGCCCACATC[A/G]TGGTGGAGGCGGCCT | 1877 |
rs756120643 | snp | A/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223070 | AAAGAATAAAACAGC[A/T]TCGCAGAGCTACCCA | 1877 |
rs756166762 | snp | C/T | 3.9116e-05 | 0.00442227 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234755 | TCGCCGAGCACGGCA[C/T]GCTGAACCGGCACCT | 1877 |
rs756206720 | snp | A/C | 1.66571e-05 | 0.00288587 | intron-variant | E4F1 | GRCh38.p7 | 16:2229557 | CTCCCCTGTTTTCTT[A/C]CCCCTTTGGCAGGTG | 1877 |
rs756210915 | snp | A/G | 1.66527e-05 | 0.00288549 | intron-variant | E4F1 | GRCh38.p7 | 16:2232915 | CACGTGCAGGTCAGC[A/G]TGGTGCGGGCAGCTG | 1877 |
rs756240490 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234238 | CCTGCTCAAGAAGCA[A/C]CAGGAGGTGCACGTG | 1877 |
rs756247708 | snp | A/C/T | 1.74598e-05 | 0.00295459 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235323 | GGAGACGGCGCTGGG[A/C/T]CCAGAGGCGGCTGCC | 1877 |
rs756271380 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222101 | GTGGCAGTTGCCTGT[A/G]GTCCCAGCTACTCAG | 1877 |
rs756300887 | snp | A/G | 6.64452e-05 | 0.00576352 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232876 | TCAGTGTGAGCAAGG[A/G]CGTGGTTGTCAGCAA | 1877 |
rs756332641 | snp | C/T | 5.19197e-05 | 0.00509482 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234190 | GAGGCCGTTCGCCTG[C/T]GCGCAGTGTGGCAAG | 1877 |
rs756353590 | snp | A/C/G | 3.97371e-05 | 0.00445727 | intron-variant | E4F1 | GRCh38.p7 | 16:2234133 | GCCTGGCGGGCCCGC[A/C/G]GGTGATGGGCTTGGC | 1877 |
rs756374186 | snp | C/T | 0.000159337 | 0.0089243 | intron-variant | E4F1 | GRCh38.p7 | 16:2223977 | GGGCGCCTGTCATCC[C/T]CCCTCTCTGGTGTGC | 1877 |
rs756439711 | snp | C/T | 7.09358e-05 | 0.00595507 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235189 | GCTCCCTGGCACAGC[C/T]GCTCTTGCTGAGCCG | 1877 |
rs756577645 | snp | A/C | 2.0649e-05 | 0.00321311 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223810 | CGGCCGGGGTGCGGG[A/C]AGTTCATCCCGGGCT | 1877 |
rs756596489 | snp | A/G | 6.91898e-05 | 0.00588134 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235116 | GACCAGTGAGGCCAC[A/G]GAGATCATCGAGGGC | 1877 |
rs756620926 | snp | A/G | 1.71502e-05 | 0.00292827 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232304 | GCAGGCCCAGGTGAA[A/G]CTACTGGTGAACAAG | 1877 |
rs756713317 | snp | C/T | 5.67628e-05 | 0.00532712 | intron-variant | E4F1 | GRCh38.p7 | 16:2233232 | TGTCTTCTGCCTGCT[C/T]GGTGCCAGTCTTTGT | 1877 |
rs756772875 | snp | C/G | 3.98589e-05 | 0.00446406 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234625 | CACCTGGAGGAGAAG[C/G]CGCACGTGTGCCAGT | 1877 |
rs756862223 | in-del | -/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229370 | CCCTGGCCCGGGGGT[-/G]GAAGGGATTGGACTG | 1877 |
rs756869236 | snp | C/T | 8.27712e-05 | 0.00643263 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235515 | CCTGGAGCATGCAGG[C/T]GAGCTGGTCATCGCC | 1877 |
rs756955653 | snp | C/T | 1.73525e-05 | 0.0029455 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228509 | CCTGCCACCACAGCG[C/T]TGCTGGGCCAGGAGG | 1877 |
rs757043640 | snp | A/C | 1.68352e-05 | 0.00290126 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228456 | ACAAGATTCAGAAGG[A/C]CTGCCAGCGGGCCCC | 1877 |
rs757045675 | snp | A/G/T | 8.46122e-05 | 0.00650383 | intron-variant | E4F1 | GRCh38.p7 | 16:2232710 | CCTTGTCACCTTGTC[A/G/T]CCAGCCTGCTGGGGC | 1877 |
rs757113467 | snp | A/C | 8.9658e-05 | 0.00669484 | intron-variant | E4F1 | GRCh38.p7 | 16:2233867 | GGTGCTGGAGACCTT[A/C]CTGTGGTTCCCCAGC | 1877 |
rs757139134 | snp | C/T | 7.07414e-05 | 0.0059469 | intron-variant | E4F1 | GRCh38.p7 | 16:2232587 | CACGGGTGAGCTGGC[C/T]GCACCTCGGGCTGGA | 1877 |
rs757172853 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224647 | CAAAAAAACAAAATT[A/G]GCCGGGCGTGGTGGC | 1877 |
rs757175068 | snp | C/T | 9.11328e-05 | 0.00674967 | synonymous-codon, stop-gained, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223670 | GGCAGAAGCCCAGGC[C/T]GAAGCCGGGCGGGAA | 1877 |