E4F1
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs26837snpA/G0.498890.0235361intron-variantE4F1GRCh38.p716:2230317AGGTCTGGATGGGCA[A/G]GCTCTCATCGGGGAC1877
rs26838snpC/G0.4995980.0141716intron-variantE4F1GRCh38.p716:2231150CTAGTGGAGATGGCA[C/G]AGGGTCCTGCCTGCT1877
rs26839snpA/G0.01335360.0806142missense, nc-transcript-variantE4F1GRCh38.p716:2232255CCCCGGGCAGCCCCC[A/G]CCAGCAGGGGCTGGG1877
rs26840snpC/T0.4774890.103676utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235356CGACACCATCACCAT[C/T]GCCACCCCCGAGAGC1877
rs27382snpA/G0.498890.0235361intron-variantE4F1GRCh38.p716:2230276GATGTCTCTCTCCCT[A/G]ATGTGCTGTGGGAGG1877
rs27709snpA/G0.4352630.167862intron-variantE4F1GRCh38.p716:2231828GCAGGACAGGCGGCT[A/G]TCTCTTCACCCAAGG1877
rs30985snpA/G0.005972470.0543191intron-variantE4F1GRCh38.p716:2226663AGTGTCAGGGACAGT[A/G]CCTGTTTACACAAAG1877
rs30986snpA/G0.4327970.170544intron-variantE4F1GRCh38.p716:2225866cctcgggatccgccc[A/G]tctcagcctcccaaa1877
rs30987snpA/G0.4999080.00678851intron-variantE4F1GRCh38.p716:2225685cgggagttcaagacc[A/G]gcctggccaacatgg1877
rs30988snpA/G0.4997590.0109798intron-variantE4F1GRCh38.p716:2224299ACCCAGGATCAAAGA[A/G]CTAGAAAGCGGCAAG1877
rs30989snpC/G0.2510140.249998upstream-variant-2KBE4F1GRCh38.p716:2221605ggagttcaagaccaa[C/G]caggccaacatggca1877
rs313910snpG/T0.1755760.238665intron-variantE4F1GRCh38.p716:2229370ACCCTGGCCCGGGGG[G/T]GAAGGGATTGGACTG1877
rs1056834snpC/G00utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235260GCAGATCGTGCACCA[C/G]GCTAGCGCCGGCCAC1877
rs1056869snpC/T00utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235620ACAGGGCAGAGGACT[C/T]TGAGCGCCCCACCCA1877
rs1612140snpA/G0.1645460.234942intron-variantE4F1GRCh38.p716:2225767AGACTGGGAGGAGCC[A/G]GGCACGGTGGCGCAC1877
rs1640780snpC/T0.1642190.234823intron-variantE4F1GRCh38.p716:2225699CTGGTCTTGAACTCC[C/T]GACCTCAGGTGATCT1877
rs1804823snpA/C/T1.84862e-050.00304019utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235483GTGACCATGGTGTCA[A/C/T]CAGAGGACATCGAGA1877
rs2241070snpA/G0.09666940.197458synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228508CCCTGCCACCACAGC[A/G]TTGCTGGGCCAGGAG1877
rs2241071snpA/G0.3733970.217424intron-variantE4F1GRCh38.p716:2229369GACCCTGGCCCGGGG[A/G]TGAAGGGATTGGACT1877
rs2302584snpA/C/T0.002074960.032143synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234763CACGGCACGCTGAAC[A/C/T]GGCACCTGCGCACCA1877
rs3096278snpC/T0.1655270.235296intron-variantE4F1GRCh38.p716:2226088TTTTTTCTTTCAAGG[C/T]GGAGTCTCGCTTTGT1877
rs3114131snpC/G0.2023430.245416intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234514TCTCCCCTCCCGCCT[C/G]TGGCCCAAGGGAGGG1877
rs8056361snpA/G0.1758970.238765upstream-variant-2KBE4F1GRCh38.p716:2222891gcctggcgtggtggc[A/G]gacacctgtagtccc1877
rs8057731snpA/G0.04791490.147179upstream-variant-2KBE4F1GRCh38.p716:2222654tggtttgaggctagg[A/G]gtttgagaccagcct1877
rs9928419snpC/Tintron-variantE4F1GRCh38.p716:2225526ttgcccaggctggag[C/T]gcaatggtgcgatct1877
rs11640867snpC/T0.0001779840.00943188intron-variantE4F1GRCh38.p716:2233668TGCCAGCACCACCTG[C/T]GGGCTCCTCCCAGGG1877
rs11641096snpA/G0.4959270.0449436upstream-variant-2KBE4F1GRCh38.p716:2221670aagtgctgggattac[A/G]ggagtgagccactgt1877
rs11648028snpC/T0.50intron-variantE4F1GRCh38.p716:2231341CCCCATCAGAGGCCT[C/T]TGTCCTTTGGAAGAT1877
rs11648224snpC/G00intron-variantE4F1GRCh38.p716:2226492TGCAGGCGAGTCATA[C/G]CTGTGGTTTGGCCCT1877
rs12935005snpC/T00intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223849CCCGGATGGCCCGAG[C/T]TGCGGGCTCGACCGA1877
rs34008168in-del-/Tintron-variantE4F1GRCh38.p716:2227844TTTTTTTTTTTTTTT[-/T]GGTAGAGATGGGTCT1877
rs34062468in-del-/Cintron-variantE4F1GRCh38.p716:2228672GGTGTGGGAGGGTCC[-/C]GGGTGTGTGAGCCTG1877
rs34166917in-del-/Tintron-variantE4F1GRCh38.p716:2231555AACCTGAACTGTGTT[-/T]ACAACCTAGCTTTGC1877
rs34243234in-del-/Tintron-variantE4F1GRCh38.p716:2225490CTTTTTTTTTTTTTT[-/T]GAGACGGCGTTTCTC1877
rs34274744in-del-/Tupstream-variant-2KBE4F1GRCh38.p716:2222930GGAGGCTGAGGCAGG[-/T]AGAATGGCGTGAACC1877
rs34615954snpC/Tintron-variantE4F1GRCh38.p716:2230274AAGATGTCTCTCTCC[C/T]TAATGTGCTGTGGGA1877
rs35080768in-del-/T00intron-variantE4F1GRCh38.p716:2227844TTTTTTTTTTTTTTT[-/T]GGTAGAGATGGGTCT1877
rs35320604in-del-/Gdownstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235867CCGCCCCACCCAGGG[-/G]CTTCTGCCAGCCCTG1877
rs35337547snpC/T0.01680550.0901129synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228385GCGGCCGCATCTGTG[C/T]ACATCGTCCTCATCT1877
rs35339015in-del-/Gintron-variantE4F1GRCh38.p716:2233814GGGTGGGGCCCATGG[-/G]TTGTGTTCTTGGTAC1877
rs35368180in-del-/GA0.4734510.112115upstream-variant-2KBE4F1GRCh38.p716:2221663CTCCCAAAGTGCTGG[-/GA]GATTACGGGAGTGAG1877
rs35436732snpC/T0.07299980.176553intron-variantE4F1GRCh38.p716:2231323CATGTTCCCCCAGGT[C/T]CTCCCCATCAGAGGC1877
rs35483132snpC/T0.08363540.186609intron-variantE4F1GRCh38.p716:2231011GCCCCTCTTGGCACC[C/T]CTGCCACTCTGGCAC1877
rs35508264snpC/G0.005284370.0511299missense, nc-transcript-variantE4F1GRCh38.p716:2233474GGTTCTCACGGCTGC[C/G]CTCGCTGGAGCAGGG1877
rs35589455in-del-/Gintron-variantE4F1GRCh38.p716:2231669CGTTCACTCTCCCAG[-/G]CCAAGCCTGCCTTGG1877
rs35739041in-del-/Cframeshift-variant, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233509CACCAGGCCATGCAG[-/C]AACTCCGGCATCGTC1877
rs56828353snpA/G0.02484320.108648intron-variantE4F1GRCh38.p716:2229845GCAGGAGGAGGAAGC[A/G]TTGGGCACTGGGCCT1877
rs57106550snpC/Tintron-variantE4F1GRCh38.p716:2225691TGGCCAGGCTGGTCT[C/T]GAACTCCCGACCTCA1877
rs57862391snpA/G/Tutr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantE4F1GRCh38.p716:2223517CTCCGGTTCTGCCCC[A/G/T]CCCTCCTCTTGCCGT1877
rs58584758snpC/T0.02523250.109451intron-variantE4F1GRCh38.p716:2234058CGGGGTGCTTCTGGG[C/T]GTCCAGGGTGGGTCC1877
rs58700030snpC/Tintron-variantE4F1GRCh38.p716:2225720CAGGTGATCTGCCCG[C/T]CTCAGCCTCCCAAAG1877
rs59007121snpC/Tintron-variantE4F1GRCh38.p716:2225714CGACCTCAGGTGATC[C/T]GCCCGCCTCAGCCTC1877
rs59101267snpA/Gintron-variantE4F1GRCh38.p716:2225865CTTTGGGAGGCTGAG[A/G]CGGGCGGATCCCGAG1877
rs59563983snpG/T0.02872840.116357intron-variantE4F1GRCh38.p716:2229747GATGGGGCCCCTGCT[G/T]CCTGTATGCTCGTCT1877
rs59620278snpA/Tintron-variantE4F1GRCh38.p716:2225661ATTTTTAGTAGAGAC[A/T]GGATTTCTCCATGTT1877
rs59759998snpC/T0.01853990.0944786intron-variantE4F1GRCh38.p716:2233843ACTGCCAGGGCACAG[C/T]CTGCCCCGGGTGCTG1877
rs59784157snpA/G/T0.01127730.0742411missense, nc-transcript-variantE4F1GRCh38.p716:2233444CCCCTGCAGCCCCCC[A/G/T]TCTCCCAGGAGCTCC1877
rs59845216snpG/T0.02445380.107838intron-variantE4F1GRCh38.p716:2233327AGGGCCAGTGGGAGC[G/T]CCATGGGGGTCTGAG1877
rs60013960in-del-/Gintron-variantE4F1GRCh38.p716:2229369ACCCTGGCCCGGGGG[-/G]TGAAGGGATTGGACT1877
rs60612119snpG/T0.0291160.117091intron-variantE4F1GRCh38.p716:2231788CCTATGTTGGTGGGA[G/T]CAGTGGCAGGAGCAG1877
rs62040662snpG/Tintron-variantE4F1GRCh38.p716:2228798TTCTTGGAGCTGGAG[G/T]GTCTCCTTTGGCTCT1877
rs71394733in-del-/A0.50intron-variantE4F1GRCh38.p716:2227024GCTCAAACTCCCGCA[-/A]GTTTTTGTTTGTTTG1877
rs72766666snpC/T0.0007984030.0199641upstream-variant-2KBE4F1GRCh38.p716:2222687TCTAAACAGCAAGAC[C/T]CTGTCTCTATTTAAA1877
rs73500107snpG/T0.0291160.117091intron-variantE4F1GRCh38.p716:2226796GGTGCTTGGCACACA[G/T]TGAGGGGGTGGTCTC1877
rs74367875snpC/T0.01820190.0936463intron-variantE4F1GRCh38.p716:2224662AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTAGTGG1877
rs74695663snpA/G0.02094210.100162downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235846CTCCTAGACTCACGT[A/G]CCTGGCCGCCCCACC1877
rs75636456snpA/G0.05246040.153226intron-variantE4F1GRCh38.p716:2231923GGTCTCCCTGTGGAC[A/G]CATTTAGGGGCCCTG1877
rs75956074snpG/T0.50intron-variantE4F1GRCh38.p716:2225489TCTTTTTTTTTTTTT[G/T]TGAGACGGCGTTTCT1877
rs76885746snpA/G0.007162660.059414intron-variantE4F1GRCh38.p716:2224387GCCAGTAATGTAACA[A/G]GCCCTTATCCTGCTT1877
rs77536843snpC/T0.009934190.0697739intron-variantE4F1GRCh38.p716:2230326TGGGCAGGCTCTCAT[C/T]GGGGACAGATGCTTG1877
rs78398423snpC/T0.03259760.123435downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235852GACTCACGTGCCTGG[C/T]CGCCCCACCCAGGGG1877
rs78729709snpG/T00intron-variantE4F1GRCh38.p716:2225491TTTTTTTTTTTTTTT[G/T]AGACGGCGTTTCTCT1877
rs79253733snpC/G0.50intron-variantE4F1GRCh38.p716:2224994AAGGTGGGTGGATCA[C/G]CTGAGGTCAGGAGTT1877
rs79982505snpA/C0.001596170.0282053intron-variantE4F1GRCh38.p716:2230456AGACGCGAGGGAAGG[A/C]GCTGTCTAGGGACCT1877
rs80084951snpA/C0.50missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233553CTGGGGAGGAGGGTG[A/C]CCTGGAGCCAGCTCC1877
rs111361324snpC/Tintron-variantE4F1GRCh38.p716:2224956AGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG1877
rs111514458snpA/G0.50utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantE4F1GRCh38.p716:2223501CCTGTCCGTCAATCC[A/G]CTCCGGTTCTGCCCC1877
rs111767084in-del-/G0.174610.238362intron-variantE4F1GRCh38.p716:2229364CGCTGACCCTGGCCC[-/G]GGGGGTGAAGGGATT1877
rs111797145snpA/C0.50intron-variantE4F1GRCh38.p716:2231330CCCCAGGTCCTCCCC[A/C]TCAGAGGCCTCTGTC1877
rs112325888in-del-/T00intron-variantE4F1GRCh38.p716:2225806AAAAAAAAAAAAAAA[-/T]AAAAAAAGGCTGGGC1877
rs112564078snpC/T0.50intron-variantE4F1GRCh38.p716:2229002CCGCACACGCCGCAG[C/T]GGGCGCTTGTCATCC1877
rs112862402snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2231823AGCGAGCAGGACAGG[C/T]GGCTGTCTCTTCACC1877
rs112919582snpA/T0.1286320.218563intron-variantE4F1GRCh38.p716:2225810AAAAAAAAAAAAAAA[A/T]AAAGGCTGGGCGCAA1877
rs112938340snpA/C/G/T0.0003028580.0123026intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234790ACCAAAGGTCTGGGC[A/C/G/T]GGTGGAGGTGGGAGG1877
rs112969870snpA/G0.50upstream-variant-2KBE4F1GRCh38.p716:2222816TCACGAGGTCAGGAG[A/G]TCGAGACCATCCTGG1877
rs113062677snpC/T0.02445380.107838intron-variantE4F1GRCh38.p716:2225144CTTGAGCCCAGGAGA[C/T]GGAGGTCGCAGTAAG1877
rs113244233snpA/G0.50intron-variantE4F1GRCh38.p716:2225497TTTTTTTTTGAGACG[A/G]CGTTTCTCTCTTGTT1877
rs113268992snpA/G0.006369360.0560724upstream-variant-2KBE4F1GRCh38.p716:2221577TTTTGTATTTTTAGT[A/G]AAGACGTAATTTTGC1877
rs113270919snpC/G/T6.98731e-050.00591036missense, synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2234184AGGGCCGAGGCCGTT[C/G/T]GCCTGCGCGCAGTGT1877
rs113465416snpA/G0.01466720.084371intron-variantE4F1GRCh38.p716:2226397GAGTAGGGTGGGAAG[A/G]GGAAGAGGGTGGTGG1877
rs113710566snpC/T0.50intron-variantE4F1GRCh38.p716:2232698TGCCTGCCTTCGCCT[C/T]GTCACCTTGTCGCCA1877
rs113976652snpA/C/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229560CCCTGTTTTCTTCCC[A/C/T]CTTTGGCAGGTGGTG1877
rs114147924snpA/G0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235854CTCACGTGCCTGGCC[A/G]CCCCACCCAGGGGCT1877
rs114578394snpA/G0.05246040.153226downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235918GGGTGTCATTGGCAT[A/G]TTGACCAACAGCCTC1877
rs115208946snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230188GTGGGAGTGGTGATT[A/G]CTACACTGGTCCTCA1877
rs115624510snpA/G0.0007208980.0189718utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235460CAAGTGGCACTGAAC[A/G]GGCCACTGTGACCAT1877
rs116064450snpG/T0.008747350.0655527upstream-variant-2KBE4F1GRCh38.p716:2223198CCCTGGTTGGAGCTG[G/T]GGCGGCTTCCCAGCA1877
rs117057799snpC/T0.0003743660.0136764intron-variantE4F1GRCh38.p716:2232371TTCAAGACGGTGAGC[C/T]GGCGTGCGGGGAGCC1877
rs117454577snpC/T0.01466720.084371intron-variantE4F1GRCh38.p716:2231966GCAGCCTGACAGAGT[C/T]GGGAGGTGTCTCTCC1877
rs137969975snpA/G0.0004666560.0152679missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2234191AGGCCGTTCGCCTGC[A/G]CGCAGTGTGGCAAGG1877
rs138184443snpA/G0.0001539880.00877327missense, nc-transcript-variantE4F1GRCh38.p716:2232186GTGGTGGGCACATCA[A/G]AGAGGTCATCGTGGC1877
rs138215085snpA/G0.0001539880.00877327synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233494CCGTGAGAACCTGCT[A/G]CACCAGGCCATGCAG1877
rs138258884snpG/T0.002791620.0372561intron-variantE4F1GRCh38.p716:2226157GTTAATGATTGGGTT[G/T]AGGGTGGTCTTGTCT1877
rs138375156snpA/G0.009998450.0699947utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235436CTGTGCTTGCCGCCC[A/G]GGCAGGGACAAGTGG1877
rs138466132snpA/G0.001197370.0244387intron-variantE4F1GRCh38.p716:2229057CTCAGAAAGTGGTCA[A/G]TGGCCTCTGGCCACC1877
rs138635935snpA/G0.0001423690.00843589synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234947GGAAGACCCGCACAC[A/G]GTGTTGGTGGAGTTC1877
rs138679168snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229300TCCCTCCCTGCAGGC[A/G]CCCTGTGCTCCAGGT1877
rs138985848snpA/C/G6.97075e-050.00590335utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235285GGCCACCAGATCATC[A/C/G]TGCAGAACGTCACCA1877
rs139395951snpA/G0.0001549950.00880189utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235404CATGACGCTGGCCTC[A/G]GCCATCAGCGAGGGC1877
rs139411986snpC/T0.0001005720.00709053synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228418CCAGGCAGAGTTCAC[C/T]GCCTTGGAGGATTTT1877
rs139438270snpA/G0.001395370.0263769synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232805GAGCTTCCGGGAGTC[A/G]GGTGCACTGACCCGG1877
rs139464530snpA/G0.002791620.0372561upstream-variant-2KBE4F1GRCh38.p716:2222289TTGGGAGGCCGAGGC[A/G]GGCAGATCGTGAGGT1877
rs139624156snpC/T0.001197370.0244387downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236221TGGCTGACCGTCTAC[C/T]TCCCTCCTAGGGGGC1877
rs139791282snpA/G0.0007984030.0199641intron-variantE4F1GRCh38.p716:2232030CCTTGGCTGTTGCTC[A/G]GACCTGTGTGTTGAG1877
rs140042589in-del-/Aintron-variantE4F1GRCh38.p716:2231274CCTGCCGCTTCGCGG[-/A]AAAAGTTCGCGTCTC1877
rs140166330snpC/T0.0001503120.00866795synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232775GCGCCCCTACAAGTG[C/T]TCCAAGTGTGGAAAG1877
rs140184126snpC/T1.67405e-050.00289309missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234312AGACCATTGCCCATG[C/T]GCGTGGCCACCGGCG1877
rs140445968snpA/G1.66032e-050.0028812missense, nc-transcript-variantE4F1GRCh38.p716:2232858GCACAGAGAAAATCC[A/G]CTTCAGTGTGAGCAA1877
rs140454954snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227363TACAGGCATGCGCCA[C/G]CAAGCCTGGCTAATA1877
rs140552076snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230126TCTCTAGCTGGGCTC[A/G]GACTTGCTGCTGGCC1877
rs140659034snpA/G0.003587790.0422022intron-variantE4F1GRCh38.p716:2228771GTGCTGTTGGGGGCC[A/G]GGATCTCTTCTTTCT1877
rs140819575snpA/G0.0004005320.0141459utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235479CACTGTGACCATGGT[A/G]TCATCAGAGGACATC1877
rs140972388snpA/G0.002245440.0334317missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234725CGTTCAAGTGCTACA[A/G]GTGCGGCCGTGGCTT1877
rs141058515snpC/G0.001197370.0244387intron-variantE4F1GRCh38.p716:2225608CCTCCTGAGTAGCTG[C/G]GATTACGGCACGCGG1877
rs141119759snpC/T0.01466720.084371intron-variantE4F1GRCh38.p716:2224769GCCTGGGCGGCAGAG[C/T]CGGACTCCGTCTCAA1877
rs141145527snpA/G0.001590950.0281592missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233534ATCGTCCTTGAGCGC[A/G]CTGCTGGGGAGGAGG1877
rs141164372snpA/G0.02289470.104514intron-variantE4F1GRCh38.p716:2227662CAAGCATGAGCCACC[A/G]CCCTAATTTTGTATT1877
rs141255210snpA/C0.002137190.0326195missense, nc-transcript-variantE4F1GRCh38.p716:2229613AGCCCATCACTGTGG[A/C]CCACATCGTGGTGGA1877
rs142130361snpC/T0.000139380.00834689utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235313CCATGGACGAGGAGA[C/T]GGCGCTGGGCCCAGA1877
rs142165926snpC/T0.0002924970.0120898missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234931CCACCACCGTCCTCA[C/T]GGAAGACCCGCACAC1877
rs142204952in-del-/A0.01898560.0955633intron-variantE4F1GRCh38.p716:2230432CAGGGGCGAGTGGCT[-/A]AGGTGTGCAGACGCG1877
rs142229326snpC/T0.0005676470.0168375synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233515GGCCATGCAGAACTC[C/T]GGCATCGTCCTTGAG1877
rs142292722snpA/G0.02211410.102801intron-variantE4F1GRCh38.p716:2224602AGACCATCCTGGCCA[A/G]CATGGTGAAACCCGT1877
rs142312413snpA/C0.003587790.0422022intron-variantE4F1GRCh38.p716:2226889TCCCAAGTCAGTGAG[A/C]AGAGTGGTTGTGGGT1877
rs142410368snpA/G0.0001748280.00934792utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235267GTGCACCAGGCTAGC[A/G]CCGGCCACCAGATCA1877
rs142656555snpA/C/T0.0002694050.0116033missense, nc-transcript-variantE4F1GRCh38.p716:2232243AGATGGCCGAGGCCC[A/C/T]GGGCAGCCCCCGCCA1877
rs142774941snpA/G0.0001539880.00877328synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234373TCCCAAGTGTGGCAA[A/G]CGCTACAAGACTAAG1877
rs142977286snpC/T5.04274e-050.00502107missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234269CGTGAGCGCCGCTTC[C/T]GCTGTGGCGACTGCG1877
rs143029764snpC/T0.02250450.103662intron-variantE4F1GRCh38.p716:2229187CCTCTGGCCCACACC[C/T]CCAGGGCCCTCTCCT1877
rs143057820snpC/T0.02250450.103662intron-variantE4F1GRCh38.p716:2228672CGGTGTGGGAGGGTC[C/T]GGGTGTGTGAGCCTG1877
rs143134295snpA/T0.0002157260.0103835synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2229587GGTGCCGGCAGCACC[A/T]GGCCCAGAGGAGCCC1877
rs143221732in-del-/Cframeshift-variant, nc-transcript-variantE4F1GRCh38.p716:2233039GCTGCCGGCTTGGGG[-/C]ACAGCCACATCATCG1877
rs143429694snpA/C/T0.000259830.0113952synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235088CTGCCCAGGCCACTG[A/C/T]GGACGATGCGGAGAC1877
rs143442513snpC/G/T0.0005965870.0172611missense, nc-transcript-variantE4F1GRCh38.p716:2232197ATCAAAGAGGTCATC[C/G/T]TGGCTGCTGAGGCGG1877
rs143899809snpC/T0.0007559680.0194271utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235573ACGGTCATCGTCTAG[C/T]ATGAGGTCTGCGGGG1877
rs143952001snpC/T3.3493e-050.00409211missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234323CATGTGCGTGGCCAC[C/T]GGCGCGTCCACTCAG1877
rs144301153snpA/Gintron-variantE4F1GRCh38.p716:2226592TGCCGAGGGACTGAA[A/G]GTGAATGGTCAGAGC1877
rs144345375snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222626AGCACTTTGGGAGGC[C/T]GAAATGGGAAAATGG1877
rs144383218snpC/T0.0001336380.00817318missense, nc-transcript-variantE4F1GRCh38.p716:2232495GTCACTCACAGCAGC[C/T]GCAAGGACCACGAGT1877
rs144477614snpA/G0.001197370.0244387intron-variantE4F1GRCh38.p716:2224616AACATGGTGAAACCC[A/G]TCTCTACTAAAAATA1877
rs144494405snpC/T1.98403e-050.00314956missense, nc-transcript-variantE4F1GRCh38.p716:2232465CCACAGGGCAGCATC[C/T]TCAAGGCCCACATGG1877
rs144562619snpC/T0.002791620.0372561intron-variantE4F1GRCh38.p716:2227572AGAGACGGGGTTTCA[C/T]GGTGTTAGCCAGGAT1877
rs144673455snpC/G/T0.0007336950.0191394utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235269GCACCAGGCTAGCGC[C/G/T]GGCCACCAGATCATC1877
rs144836270snpC/T3.34924e-050.00409208missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234326GTGCGTGGCCACCGG[C/T]GCGTCCACTCAGACG1877
rs144878577snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228262GAAGTAGCTCTGCTT[C/T]TGATGGCCTCCTGGG1877
rs144964049snpG/T6.96173e-050.00589947missense, nc-transcript-variantE4F1GRCh38.p716:2228511TGCCACCACAGCGTT[G/T]CTGGGCCAGGAGGTG1877
rs144987188snpA/G0.005575420.0525036upstream-variant-2KBE4F1GRCh38.p716:2223485CAGGCCCGGCTCCCC[A/G]CCTGTCCGTCAATCC1877
rs145239569snpC/T1.66225e-050.00288287synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232886CAAGGACGTGGTTGT[C/T]AGCAAAGAGGACGCA1877
rs145769654snpA/G0.007796560.0619475missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233522CAGAACTCCGGCATC[A/G]TCCTTGAGCGCGCTG1877
rs145913612snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228877CACACAGTCCCTAGG[A/G]ACTTCACACGTGAAG1877
rs146111343snpC/T0.0002682850.0115789synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234283CCGCTGTGGCGACTG[C/T]GGGAAGCTCTACAAG1877
rs146160872snpA/G9.37321e-050.00684524synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232509CCGCAAGGACCACGA[A/G]TGCAAGCTCTGTGGG1877
rs146307162snpA/G0.0007984030.0199641upstream-variant-2KBE4F1GRCh38.p716:2221934CTGTTTCAAAAAAAA[A/G]TCTGGCCAGGCTCGG1877
rs146393111snpA/G0.01976870.0974348intron-variantE4F1GRCh38.p716:2225966GCCGTGGTGGCAGGC[A/G]CCTGTAGTCACAGCT1877
rs146632512snpC/G0.002889650.0379008synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228493GGCCCTGCCTGCCAC[C/G]CCTGCCACCACAGCG1877
rs146690492snpA/G0.01466720.084371intron-variantE4F1GRCh38.p716:2233344CATGGGGGTCTGAGG[A/G]TTTGCACAAGGCTCC1877
rs146861908snpA/G0.01859380.0946107intron-variantE4F1GRCh38.p716:2228702GTGGTGCTCTGGGGC[A/G]TCCTGGAGGGCCTGC1877
rs146976541snpC/T0.0006089470.0174385synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233489GGCAGCCGTGAGAAC[C/T]TGCTGCACCAGGCCA1877
rs147019267snpA/G0.0003316860.0128737missense, nc-transcript-variantE4F1GRCh38.p716:2229624GTGGCCCACATCGTG[A/G]TGGAGGCGGCCTCTC1877
rs147071848snpC/T0.01267680.0785984synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234938CGTCCTCACGGAAGA[C/T]CCGCACACAGTGTTG1877
rs147409290snpC/T0.001994810.0315187utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235687GGAGGCGCCCCAAGA[C/T]GGACAGTGTACATAA1877
rs147438958snpC/G0.002791620.0372561intron-variantE4F1GRCh38.p716:2231402CGGGCAGGAGAGGCT[C/G]TTAATTGTTTCTGAG1877
rs147602177snpC/T0.0001559880.00883004synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234729CAAGTGCTACAAGTG[C/T]GGCCGTGGCTTCGCC1877
rs147847239snpA/C0.001994810.0315187intron-variantE4F1GRCh38.p716:2227605TCTCAATCTCCTGAC[A/C]TCATGATCCGCCCGC1877
rs148003042snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225242TTGTGTGTCATGTGC[C/T]GAGAGCAGTGTTGGG1877
rs148011220snpC/G/T1.75213e-050.00295978utr-variant-3-prime, missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235251GGTGGTGCAGCAGAT[C/G/T]GTGCACCAGGCTAGC1877
rs148206065snpC/T0.0002441410.0110458missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233531GGCATCGTCCTTGAG[C/T]GCGCTGCTGGGGAGG1877
rs148259822snpA/G0.001210020.0245672missense, nc-transcript-variantE4F1GRCh38.p716:2229612GAGCCCATCACTGTG[A/G]CCCACATCGTGGTGG1877
rs148311962snpC/T0.0003517260.0132567synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234340GCGCGTCCACTCAGA[C/T]GAGCGGCCCTACCCT1877
rs148570427snpG/T1.95448e-050.00312602missense, nc-transcript-variantE4F1GRCh38.p716:2232480CTCAAGGCCCACATG[G/T]TCACTCACAGCAGCC1877
rs148750102snpC/T0.006766090.0577691intron-variantE4F1GRCh38.p716:2226737GGGAATAGTTCTCTC[C/T]ATTTCCACAGGGTGC1877
rs148830665snpA/C/G0.0002202640.0104922intron-variant, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234999CAGGAGTATATCATC[A/C/G]AGGTGGGTGTGGGGC1877
rs148945075snpC/G1.66128e-050.00288204missense, nc-transcript-variantE4F1GRCh38.p716:2229579TGGCAGGTGGTGCCG[C/G]CAGCACCAGGCCCAG1877
rs149258624snpC/G/T8.45753e-050.00650245synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232274GCAGGGGCTGGGGCT[C/G/T]GCAGGGGAGGGTGAG1877
rs149377192snpA/G0.0006478780.0179866synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2229575CCTTTGGCAGGTGGT[A/G]CCGGCAGCACCAGGC1877
rs149872852snpA/C/G0.004783640.0487146intron-variantE4F1GRCh38.p716:2228224CCTTGTTTTGGGCCC[A/C/G]AGTGTGTTCTCAGCA1877
rs149925798snpC/T0.001596170.0282053upstream-variant-2KBE4F1GRCh38.p716:2223299TCCGCTCGCCCCTCG[C/T]GTTCTCTGGCTCTCA1877
rs150020970snpC/T4.98326e-050.00499138synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232877CAGTGTGAGCAAGGA[C/T]GTGGTTGTCAGCAAA1877
rs150196644snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229191TGGCCCACACCTCCA[A/G]GGCCCTCTCCTCACA1877
rs150565666snpC/T0.003587790.0422022intron-variantE4F1GRCh38.p716:2226964TCTCCTGGGCCCCAG[C/T]CCATTTTACAGATGA1877
rs150638846snpA/G0.01545380.0865337upstream-variant-2KBE4F1GRCh38.p716:2222850TCACGGTGAAACCCC[A/G]TCTCTACTAAAAATA1877
rs150753552snpA/G/T0.0006693710.0182833missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233897CAGGTGGCCAGCGAG[A/G/T]CCTCAGCGGTGCCCA1877
rs150933849snpA/G0.01911390.0958728intron-variantE4F1GRCh38.p716:2232600GCCGCACCTCGGGCT[A/G]GAGCCCGGTAGCACC1877
rs151069167snpC/T0.0005108960.0159746synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234630GGAGGAGAAGCCGCA[C/T]GTGTGCCAGTTCTGC1877
rs180969770snpA/G0.004383320.0466095intron-variantE4F1GRCh38.p716:2227060TTTTTGTTTCTTTTA[A/G]GGCAGGGTCTTGCCC1877
rs181261942snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227253CTCTCTCTGTTGCCC[C/T]GGCTGGAGTGCAATG1877
rs181388128snpA/G/T0.001197370.0244387intron-variantE4F1GRCh38.p716:2231625AAGCCCAGCTTCCTC[A/G/T]CCTCAGGCTGTCCCG1877
rs182042349snpC/G/T0.0009496040.0217695intron-variantE4F1GRCh38.p716:2232921CAGGTCAGCATGGTG[C/G/T]GGGCAGCTGCCTGGT1877
rs182105825snpA/G0.0007984030.0199641downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235979GCTGCGCTGCCTGAG[A/G]CCTGTGGGTGGGTGG1877
rs182234785snpA/G0.001549440.0277907intron-variantE4F1GRCh38.p716:2229683CCTTGTTGGTAAGCC[A/G]ACTTCCATGAATCGC1877
rs182468779snpC/Tintron-variantE4F1GRCh38.p716:2230297CTGTGGGAGGGGCTG[C/T]TGCGAGGTCTGGATG1877
rs183058723snpA/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2221825TAGCTAGTGATGGGC[A/G]CCTGTAGTCCCAGCT1877
rs183233336snpC/T0.0001045460.00722925utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235318GACGAGGAGACGGCG[C/T]TGGGCCCAGAGGCGG1877
rs183960132snpA/G0.001197370.0244387intron-variantE4F1GRCh38.p716:2230893TCCTTAGGTTCTGGC[A/G]GGGTCTCTGGGCTGG1877
rs184018937snpC/T0.002791620.0372561intron-variantE4F1GRCh38.p716:2227689TATTTTTAGTAGAGA[C/T]GGGATTTCACCATAT1877
rs184022099snpA/G0.0007984030.0199641upstream-variant-2KBE4F1GRCh38.p716:2222749AAAAAGTGGCTGGGC[A/G]CGGTGGCTCACGCCT1877
rs184349576snpA/G0.005575420.0525036intron-variantE4F1GRCh38.p716:2224771CTGGGCGGCAGAGCC[A/G]GACTCCGTCTCAAAA1877
rs185025443snpC/G0.009538730.0683987intron-variantE4F1GRCh38.p716:2230631GCTGCAGCAGGAAGA[C/G]GGGGTGGAGGAGCCG1877
rs185139637snpC/T0.001596170.0282053intron-variantE4F1GRCh38.p716:2227063TTGTTTCTTTTAAGG[C/T]AGGGTCTTGCCCTGT1877
rs185238292snpA/C/T0.0003798270.0137759utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235494GTCATCAGAGGACAT[A/C/T]GAGATCCTGGAGCAT1877
rs185596737snpA/G0.001596170.0282053intron-variantE4F1GRCh38.p716:2225578TCCCGGGTTCAAGCT[A/G]TTCTCCTGACTCGGC1877
rs185622017snpA/G0.007162660.059414intron-variantE4F1GRCh38.p716:2231743AGCCCATCTCCTCCG[A/G]TGGAAGAGTGGCCCC1877
rs186246061snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227472TGCCTGCCGGGTTCA[C/T]GCCATTCTCCTGCCT1877
rs186472853snpA/T0.001596170.0282053intron-variantE4F1GRCh38.p716:2229945GTCAGCTTTCCCGGG[A/T]GGTCTCTGCCGTGTC1877
rs186588193snpA/G0.0009709810.0220124missense, nc-transcript-variantE4F1GRCh38.p716:2233163GAGCTGTCCCTGGGC[A/G]TGAAAGCCCTGGCCC1877
rs187072710snpA/G0.02591420.11084intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223803GAGGGTGCGGCCGGG[A/G]TGCGGGCAGTTCATC1877
rs187350610snpC/T0.0007984030.0199641upstream-variant-2KBE4F1GRCh38.p716:2222228CTCCATCTCAAAAAA[C/T]AAAAACAGGCCGGGC1877
rs187574364snpG/T0.007162660.059414intron-variantE4F1GRCh38.p716:2227856TTTTGGTAGAGATGG[G/T]TCTTGCTATGTTGAC1877
rs187721152snpA/G0.0007984030.0199641upstream-variant-2KBE4F1GRCh38.p716:2223052AAAAATTAAAAGTAT[A/G]TAAAAGAATAAAACA1877
rs188243983snpC/Tintron-variantE4F1GRCh38.p716:2231264TCCAGGCCCTCCTGC[C/T]GCTTCGCGGAAAAAG1877
rs188315191snpG/T0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236026GACAGGGAGATCTGG[G/T]AGCCTCGGCCTCCAC1877
rs188481446snpC/T0.001197370.0244387intron-variantE4F1GRCh38.p716:2230584GGTTTGGGCACCAGG[C/T]GGAACCTGGCCTTGG1877
rs188680732snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227178ACTACAGGTGCATGC[C/T]GCCACACTTCCACGC1877
rs188929679snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225231AAGAAAAAAGATTGT[A/G]TGTCATGTGCCGAGA1877
rs189461001snpC/T0.02179370.102088intron-variantE4F1GRCh38.p716:2232374AAGACGGTGAGCCGG[C/T]GTGCGGGGAGCCAGT1877
rs189621252snpC/T0.006766090.0577691utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235731CTTTACAATAAAACA[C/T]GAGAACCTGCAGCTT1877
rs190273343snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226483GGTGGCCCCTGCAGG[C/T]GAGTCATAGCTGTGG1877
rs190672620snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230775CCAAGACACTCATCA[A/G]TGCCACTCAGAGCTC1877
rs191517583snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224466ATTCTCATTTTGGGG[A/G]TGAGGAAAATCGAAG1877
rs191783987snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2227618ACCTCATGATCCGCC[C/T]GCTTCAGCCTCCCAA1877
rs191847193snpA/G0.000871460.0208559synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228412CCGCTGCCAGGCAGA[A/G]TTCACCGCCTTGGAG1877
rs191872870snpC/Tintron-variantE4F1GRCh38.p716:2230001TGCCACCCCCTGGTT[C/T]CTGCTCCCTGCCCGT1877
rs192115590snpA/G0.0007984030.0199641upstream-variant-2KBE4F1GRCh38.p716:2222487TTGCACTCCAGCCTA[A/G]GTGATAGAGTGAGAC1877
rs192315662snpC/T0.009934190.0697739intron-variantE4F1GRCh38.p716:2234043TGGGCTATAGGTGGC[C/T]GGGGTGCTTCTGGGT1877
rs192547239snpA/Gdownstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236186AGGGGCGAGGACAAG[A/G]ACACAGCCGCACCGG1877
rs192654052snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2223101TGAGCCATCCCCGAC[C/T]CGTGTTCTTTTCCCG1877
rs193007268snpC/T0.009143120.0669923intron-variantE4F1GRCh38.p716:2230864GGATGGTGGCGTCAC[C/T]TGGGAGCATGAACTC1877
rs193133812snpC/Gintron-variantE4F1GRCh38.p716:2225468AGTAAGACCCCGTCT[C/G]TATTTTCTTTTTTTT1877
rs193174002snpA/T0.007955320.062565intron-variantE4F1GRCh38.p716:2230591GCACCAGGCGGAACC[A/T]GGCCTTGGGCAGCCC1877
rs199569337in-del-/Cintron-variantE4F1GRCh38.p716:2229366CTGACCCTGGCCCGG[-/C]GGGTGAAGGGATTGG1877
rs199627791snpC/T0.001130620.0237493missense, nc-transcript-variantE4F1GRCh38.p716:2232902AGCAAAGAGGACGCA[C/T]GTGCAGGTCAGCATG1877
rs199667792snpC/T0.0001173270.0076583intron-variantE4F1GRCh38.p716:2232962GGCTGTGGACGCAGC[C/T]GCCACTGGGGTGTGT1877
rs199723355snpC/G1.80896e-050.0030074utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235327ACGGCGCTGGGCCCA[C/G]AGGCGGCTGCCGCCG1877
rs199776709snpA/G0.001819690.0301087synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233950CAGTGAGACCTTCCC[A/G]ACAGCAGCCACCCTG1877
rs199803798snpA/G1.6659e-050.00288604missense, nc-transcript-variantE4F1GRCh38.p716:2232786AGTGCTCCAAGTGTG[A/G]AAAGAGCTTCCGGGA1877
rs199977994snpA/C/G0.0001395420.00835191utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235447GCCCGGGCAGGGACA[A/C/G]GTGGCACTGAACAGG1877
rs200030854snpA/G6.85248e-050.00585301missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2234201CCTGCGCGCAGTGTG[A/G]CAAGGCCTTCCCCAA1877
rs200055937snpC/T1.66355e-050.002884synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233108CCTGGTGACAGATGC[C/T]AAGGGCACCGTCATC1877
rs200137506snpA/G0.001051240.0229023utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235368CATCGCCACCCCCGA[A/G]AGCCTGACAGAGCAG1877
rs200190676snpC/T0.0001287870.00802353missense, nc-transcript-variantE4F1GRCh38.p716:2233441CCTCCCCTGCAGCCC[C/T]CCGTCTCCCAGGAGC1877
rs200233950snpC/G/T0.005431490.05183missense, nc-transcript-variantE4F1GRCh38.p716:2233460TCTCCCAGGAGCTCC[C/G/T]CTGCTCCAGCGAGGG1877
rs200326283snpA/G0.0006300990.0177384missense, nc-transcript-variantE4F1GRCh38.p716:2229628CCCACATCGTGGTGG[A/G]GGCGGCCTCTCTGGC1877
rs200374361in-del-/Tintron-variantE4F1GRCh38.p716:2225810AAAAAAAAAAAAAAA[-/T]AAAGGCTGGGCGCAA1877
rs200467051snpC/T0.0001165480.00763285intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235023GTGGGGCCCTGGGGC[C/T]GTGCTGGGACCCAGG1877
rs200493907snpC/T0.0001213960.00778995intron-variantE4F1GRCh38.p716:2233840GGTACTGCCAGGGCA[C/T]AGCCTGCCCCGGGTG1877
rs200534216snpC/T3.9797e-050.0044606missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234626ACCTGGAGGAGAAGC[C/T]GCACGTGTGCCAGTT1877
rs200695415snpC/T0.0005247330.0161892utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235606CTGGCCGGGCAGGGA[C/T]AGGGCAGAGGACTCT1877
rs200728691in-del-/T0.009934190.0697739intron-variantE4F1GRCh38.p716:2225330CTGTACCCTCTGAGC[-/T]TTGTCCTATGAGGCT1877
rs200758185snpA/G0.0007984030.0199641missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234751GGCTTCGCCGAGCAC[A/G]GCACGCTGAACCGGC1877
rs200831818snpA/C0.001106020.0234901missense, nc-transcript-variantE4F1GRCh38.p716:2223675AAGCCCAGGCCGAAG[A/C]CGGGCGGGAAGCGGG1877
rs200965712snpC/T0.0003992810.0141238missense, nc-transcript-variantE4F1GRCh38.p716:2233053GGACAGCCACATCAT[C/T]GGTGACAGGCGAGCC1877
rs200987209snpA/G0.0005515030.0165966intron-variantE4F1GRCh38.p716:2232941AGCTGCCTGGTCCTG[A/G]GGGCTGGCTGTGGAC1877
rs201011998snpA/T0.002995490.0385846utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235369ATCGCCACCCCCGAG[A/T]GCCTGACAGAGCAGG1877
rs201223947snpC/T0.0003334630.0129081utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235527AGGCGAGCTGGTCAT[C/T]GCCTCGCCGGAGGGC1877
rs201269196snpA/G0.0001586620.00890537intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235162AGGGGTAGGGCAGGC[A/G]GGGGCGGGGAGGCTC1877
rs201296918snpC/T0.001743680.0294754missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233637TACTGGAAGTGCAGC[C/T]GCTGGAGACAGTAGG1877
rs201442335snpA/G1.72142e-050.00293374utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235392AGAGCAGGTGGCCAT[A/G]ACGCTGGCCTCGGCC1877
rs201499569snpC/G1.67947e-050.00289777missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234273AGCGCCGCTTCCGCT[C/G]TGGCGACTGCGGGAA1877
rs201519515snpC/T6.64044e-050.00576175missense, nc-transcript-variantE4F1GRCh38.p716:2232857TGCACAGAGAAAATC[C/T]GCTTCAGTGTGAGCA1877
rs201716081snpC/T4.17232e-050.00456726synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233963CCGACAGCAGCCACC[C/T]TGGAGGCCCACAAGA1877
rs201773481snpC/T0.0006838750.0184789missense, nc-transcript-variantE4F1GRCh38.p716:2233047GCTTGGGGACAGCCA[C/T]ATCATCGGTGACAGG1877
rs201928284snpC/T1.84599e-050.00303803utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235331CGCTGGGCCCAGAGG[C/T]GGCTGCCGCCGACAC1877
rs201979006snpA/G7.65404e-050.00618582intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235024TGGGGCCCTGGGGCC[A/G]TGCTGGGACCCAGGG1877
rs202007289snpA/T0.001140450.0238522intron-variantE4F1GRCh38.p716:2228527CTGGGCCAGGAGGTG[A/T]GCCCTCACCCACTCC1877
rs202118148snpA/G3.57079e-050.00422524intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235047ACCCAGGGGCAGCCA[A/G]GGCTGACCTCTGTCC1877
rs367646024snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2222550AAAACCAAAAACAAC[C/T]CCCATCTCCAAAACC1877
rs367749621snpA/C0.0001539880.00877328intron-variantE4F1GRCh38.p716:2229690GGTAAGCCGACTTCC[A/C]TGAATCGCTGGCCTG1877
rs367946733snpC/G/T0.0001383960.00831759missense, nc-transcript-variantE4F1GRCh38.p716:2228507CCCCTGCCACCACAG[C/G/T]GTTGCTGGGCCAGGA1877
rs367999348snpC/Tintron-variantE4F1GRCh38.p716:2229859CGTTGGGCACTGGGC[C/T]TTCCTCAGGTGTCCA1877
rs368082034snpA/C0.0001599870.00894248missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233585GCTGCCGGGTCCAGT[A/C]CCCAGCCCCTGGCAG1877
rs368189091snpC/T0.0002584940.0113657utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235413GGCCTCGGCCATCAG[C/T]GAGGGCACTGTGCTT1877
rs368381184snpA/G0.0001539880.00877327synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233923GCCCAGGACCCACCC[A/G]TGTCCTCAGTGCAGT1877
rs368382659snpC/T0.0004258580.0145859synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233533CATCGTCCTTGAGCG[C/T]GCTGCTGGGGAGGAG1877
rs368408185snpC/T0.0001021240.00714504synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228379CGTTGCAGATGAGGA[C/T]GATGTGCACAGATGC1877
rs368692876snpA/Gintron-variantE4F1GRCh38.p716:2227967CCATGCCCGGCCCCA[A/G]CAGTCTTAAATCCTG1877
rs368693289snpA/C/G8.4334e-050.00649313missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2234251CACCAGGAGGTGCAC[A/C/G]TGCGTGAGCGCCGCT1877
rs368730551snpC/T0.000158190.00889214intron-variant, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234963GTGTTGGTGGAGTTC[C/T]CGTCCGTGGTAGCTG1877
rs368979736snpA/G1.6676e-050.00288751intron-variantE4F1GRCh38.p716:2229549ACAGACGACTCCCCT[A/G]TTTTCTTCCCCCTTT1877
rs368981200snpA/Gintron-variantE4F1GRCh38.p716:2227322TGAAGTGATTCTCCT[A/G]CCTCAGCCTCTCGAA1877
rs369048199snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2222372AATACAAAAATTAGC[C/T]GGCCATGGTGGTGCA1877
rs369105592snpA/G0.0002532350.0112496utr-variant-5-prime, missense, nc-transcript-variantE4F1GRCh38.p716:2223576TTGTTATGACGACAT[A/G]GTCGTAAATCCGCCA1877
rs369250307snpC/G1.66134e-050.00288208missense, nc-transcript-variantE4F1GRCh38.p716:2232881GTGAGCAAGGACGTG[C/G]TTGTCAGCAAAGAGG1877
rs369253796snpC/G1.74388e-050.00295281intron-variantE4F1GRCh38.p716:2232144CAGGGGCAGGTCCTG[C/G]GGCTTAGGCCCAGAT1877
rs369255809snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2222914GTAGTCCCAGCTACT[C/T]AGGAGGCTGAGGCAG1877
rs369256860snpG/Tintron-variantE4F1GRCh38.p716:2230412CTGCTGGGGTTGGGG[G/T]TGCGGCAGGGGCGAG1877
rs369274242snpC/T1.66452e-050.00288484synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233117AGATGCCAAGGGCAC[C/T]GTCATCCACGAAGTC1877
rs369317092snpA/G0.0001331580.00815851missense, nc-transcript-variantE4F1GRCh38.p716:2233118GATGCCAAGGGCACC[A/G]TCATCCACGAAGTCC1877
rs369334404snpC/T0.0001005680.00709042synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233989CAAGAGGGGCCACAC[C/T]GGTAGGTGATGGGTG1877
rs369411860snpC/T0.0002858080.0119508intron-variantE4F1GRCh38.p716:2232751TGACTAGGTTCTCTC[C/T]GCAGATGAGCGCCCC1877
rs369465221snpC/T0.0002105340.0102578utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235341AGAGGCGGCTGCCGC[C/T]GACACCATCACCATC1877
rs369469139snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2222978AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG1877
rs369561300snpC/T0.0009270180.0215093intron-variant, synonymous-codonE4F1GRCh38.p716:2228334TGGCTGCCCAGCCTC[C/T]GCCTTCCCAGGCCCT1877
rs369593675snpC/T6.64386e-050.00576323synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2229659AGCAGACATCAGCCA[C/T]GCATCTGACCTTGTT1877
rs369630364snpA/G6.90107e-050.00587372utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235533GCTGGTCATCGCCTC[A/G]CCGGAGGGCCAGCTG1877
rs369695932snpA/G1.67416e-050.00289318missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234302AAGCTCTACAAGACC[A/G]TTGCCCATGTGCGTG1877
rs369921174snpA/Cintron-variantE4F1GRCh38.p716:2226636TGGAAGCAGAAGAAA[A/C]AGCTCCTATCCCTTT1877
rs369951581snpC/T0.0001539880.00877327intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235167TAGGGCAGGCGGGGG[C/T]GGGGAGGCTCCCTGG1877
rs370107044snpA/G1.66466e-050.00288496splice-donor-variantE4F1GRCh38.p716:2229676CATCTGACCTTGTTG[A/G]TAAGCCGACTTCCAT1877
rs370129492snpA/G2.17143e-050.00329495synonymous-codon, missense, nc-transcript-variantE4F1GRCh38.p716:2223658GGCCGCTCATACGGC[A/G]GAAGCCCAGGCCGAA1877
rs370199008snpA/C0.0001539880.00877327intron-variantE4F1GRCh38.p716:2232370CTTCAAGACGGTGAG[A/C]CGGCGTGCGGGGAGC1877
rs370269815snpC/T0.0001599870.00894249synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234902GCTGGTGTCTGAGGA[C/T]AGCCCCGCGGCAGCC1877
rs370499012snpC/Tmissense, nc-transcript-variantE4F1GRCh38.p716:2232818TCGGGTGCACTGACC[C/T]GGCACCTCAAGTCTC1877
rs370510459snpC/T1.72994e-050.00294099missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235092CCAGGCCACTGCGGA[C/T]GATGCGGAGACCAGT1877
rs370525100snpC/G0.000443960.0148924intron-variantE4F1GRCh38.p716:2232451TGCCACGCCCTCCCC[C/G]ACAGGGCAGCATCCT1877
rs370540960snpA/G0.0007092680.0188184intron-variantE4F1GRCh38.p716:2232953CTGGGGGCTGGCTGT[A/G]GACGCAGCCGCCACT1877
rs370544239snpC/G/T5.22656e-050.0051118utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235316TGGACGAGGAGACGG[C/G/T]GCTGGGCCCAGAGGC1877
rs370653709snpA/G0.001229860.0247673synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233596CAGTCCCCAGCCCCT[A/G]GCAGTGGCAGCCCCG1877
rs370693095snpG/Tintron-variantE4F1GRCh38.p716:2233306TGGGCTTCCCACAGG[G/T]AGAGCAGGGCCAGTG1877
rs370702358snpA/G0.003189780.0398085intron-variantE4F1GRCh38.p716:2231205AGGTCCTGTCTTTGC[A/G]GGTGCAGGGGTGCGG1877
rs370764054snpC/T2.50636e-050.00353994synonymous-codon, stop-gained, nc-transcript-variantE4F1GRCh38.p716:2223691CGGGCGGGAAGCGGG[C/T]GAGGGTGCAGTTGCG1877
rs370872113snpC/G3.32862e-050.00407946missense, nc-transcript-variantE4F1GRCh38.p716:2232908GAGGACGCACGTGCA[C/G]GTCAGCATGGTGCGG1877
rs370894816in-del-/Aintron-variantE4F1GRCh38.p716:2226109AAGAAAAAAAAAAAA[-/A]GATGCAGATTGGGTC1877
rs370942286snpA/G/T9.96808e-050.00705916intron-variantE4F1GRCh38.p716:2232375AGACGGTGAGCCGGC[A/G/T]TGCGGGGAGCCAGTG1877
rs371012550snpC/Tintron-variantE4F1GRCh38.p716:2231731CTGCAGTGGCCCAGC[C/T]CATCTCCTCCGATGG1877
rs371113367snpA/G0.0003362740.0129624intron-variantE4F1GRCh38.p716:2233189GGCCCCAGAGGTGGG[A/G]GCGACGGGGGGCCCC1877
rs371173319snpC/Gintron-variantE4F1GRCh38.p716:2225322AGCTTGGGTCTGTAC[C/G]CTCTGAGCTTGTCCT1877
rs371251950snpA/G1.66233e-050.00288295missense, nc-transcript-variantE4F1GRCh38.p716:2232887AAGGACGTGGTTGTC[A/G]GCAAAGAGGACGCAC1877
rs371289726snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228755CCTCTGGTCGAAGCC[C/T]GTGCTGTTGGGGGCC1877
rs371302779snpC/T0.001994810.0315187intron-variantE4F1GRCh38.p716:2227878TATGTTGACCAGGCT[C/T]GTCTTGAACTCCTGG1877
rs371317212snpC/G0.0003992810.0141238utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantE4F1GRCh38.p716:2223540CTTGCCGTTCCCTCA[C/G]GCTGGCCTCGGCGCG1877
rs371327894snpC/G2.23082e-050.0033397utr-variant-5-prime, synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2223606ATCTTCCTGCGGCGC[C/G]TTGCGACATGGAGGG1877
rs371331210snpC/Tintron-variantE4F1GRCh38.p716:2230541CGGGGCTGAGGCAGG[C/T]GGGGAGTGGGCAGCT1877
rs371440042snpA/C/T8.85283e-050.00665261intron-variantE4F1GRCh38.p716:2232606CCTCGGGCTGGAGCC[A/C/T]GGTAGCACCCCGATG1877
rs371527360snpA/G7.02502e-050.00592623utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235536GGTCATCGCCTCGCC[A/G]GAGGGCCAGCTGGAG1877
rs371666989snpA/Gintron-variantE4F1GRCh38.p716:2229436CACCCCAGCCGTCCC[A/G]AGGACGTGGACCCAG1877
rs371734250snpA/G5.41658e-050.00520384utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235477GCCACTGTGACCATG[A/G]TGTCATCAGAGGACA1877
rs371822192snpG/T0.0001746630.00934351synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228514CACCACAGCGTTGCT[G/T]GGCCAGGAGGTGAGC1877
rs371833339snpG/T0.0002188860.0104592intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235037CCGTGCTGGGACCCA[G/T]GGGCAGCCAAGGCTG1877
rs371851922snpA/Gsynonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234756CGCCGAGCACGGCAC[A/G]CTGAACCGGCACCTG1877
rs371870350snpC/T4.98583e-050.00499266synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233084TATAGAGACTTCACC[C/T]GTGATTCACCTGGTG1877
rs372004326snpC/G0.0001539880.00877327missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233928GGACCCACCCATGTC[C/G]TCAGTGCAGTGAGAC1877
rs372071032snpA/G0.0001539880.00877328intron-variantE4F1GRCh38.p716:2229725ACCTTCGTGGTTGGG[A/G]CCAGAGGATGGGGCC1877
rs372248982snpA/G1.66921e-050.00288891missense, nc-transcript-variantE4F1GRCh38.p716:2233011CACTCCACCTTGAAG[A/G]TTCTGGAGCTGGAGC1877
rs372279499snpC/T0.0007984030.0199641upstream-variant-2KBE4F1GRCh38.p716:2223350CATAGGTCCTTCTGC[C/T]GCCCCGCCCCCTGGC1877
rs372298010snpC/T5.09507e-050.00504705synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228382TGCAGATGAGGACGA[C/T]GTGCACAGATGCGGC1877
rs372319086snpC/T1.65855e-050.00287967missense, nc-transcript-variantE4F1GRCh38.p716:2229600CCAGGCCCAGAGGAG[C/T]CCATCACTGTGGCCC1877
rs372466046snpA/Gintron-variantE4F1GRCh38.p716:2229803AGGGGCCGCGGCCTC[A/G]TGGCAGCCTTTCTGC1877
rs372469137snpA/Gupstream-variant-2KBE4F1GRCh38.p716:2222379AAATTAGCTGGCCAT[A/G]GTGGTGCACTCCTGT1877
rs372658146snpA/G0.0005507660.0165855intron-variant, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234969GTGGAGTTCTCGTCC[A/G]TGGTAGCTGACACCC1877
rs372663046snpA/G0.004780850.0486577intron-variantE4F1GRCh38.p716:2233708AGGGGCTGTCCCCAC[A/G]CTGGCCTTCGCCTCC1877
rs372690984snpA/Gintron-variantE4F1GRCh38.p716:2234044GGGCTATAGGTGGCC[A/G]GGGTGCTTCTGGGTG1877
rs372723793snpG/Tupstream-variant-2KBE4F1GRCh38.p716:2222993CGCCACTGCACTCCA[G/T]CCTGGGCGATAGAAA1877
rs372816133snpA/Gintron-variantE4F1GRCh38.p716:2231048GATTTTCCCCTTTGC[A/G]GGCATCCTGGGTACT1877
rs372896150snpA/G0.0001539880.00877328intron-variantE4F1GRCh38.p716:2232752GACTAGGTTCTCTCT[A/G]CAGATGAGCGCCCCT1877
rs372959140snpA/G0.0001539880.00877327intron-variantE4F1GRCh38.p716:2232372TCAAGACGGTGAGCC[A/G]GCGTGCGGGGAGCCA1877
rs373086605snpA/G0.000106510.00729681intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235181GCGGGGAGGCTCCCT[A/G]GCACAGCCGCTCTTG1877
rs373113928snpC/T0.0002588730.0113741intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234402AGGTGGGTCTCTGGC[C/T]GCAGGACCCTGGCGC1877
rs373165341snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231265CCAGGCCCTCCTGCC[A/G]CTTCGCGGAAAAAGT1877
rs373212668snpA/C4.02779e-050.00448746missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234617TCAGGACACACCTGG[A/C]GGAGAAGCCGCACGT1877
rs373356413snpA/G3.7035e-050.00430304utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235597TGCGGGGTCCTGGCC[A/G]GGCAGGGACAGGGCA1877
rs373359809snpC/T5.32212e-050.00515827intron-variantE4F1GRCh38.p716:2233191CCCCAGAGGTGGGGG[C/T]GACGGGGGGCCCCGG1877
rs373362876in-delGG/Tintron-variantE4F1GRCh38.p716:2229370ACCCTGGCCCGGGGG[GG/T]GAAGGGATTGGACTG1877
rs373383344snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224372GGGGCGGCGGCTTCT[A/G]CCAGTAATGTAACAA1877
rs373465934snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226708CCTTGAACTTCAGGT[C/G]ATTTTCCTAGGATGG1877
rs373679522snpA/G3.37587e-050.00410831intron-variantE4F1GRCh38.p716:2232955GGGGGCTGGCTGTGG[A/G]CGCAGCCGCCACTGG1877
rs373733992snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228951CTTTGCTGAGCCCCA[C/T]GCCCAGCTTGGGCTG1877
rs373873519snpC/T3.55221e-050.00421424intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235183GGGGAGGCTCCCTGG[C/T]ACAGCCGCTCTTGCT1877
rs373947740snpC/T5.22207e-050.00510956utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235305GAACGTCACCATGGA[C/T]GAGGAGACGGCGCTG1877
rs374094183snpC/T0.001596170.0282053upstream-variant-2KBE4F1GRCh38.p716:2222074AAAATATAAAAAAAT[C/T]AGCCGGGTGTGGTGG1877
rs374158929snpA/G0.0001559880.00883005intron-variantE4F1GRCh38.p716:2232138TCTGGACAGGGGCAG[A/G]TCCTGGGGCTTAGGC1877
rs374328393snpC/G/T8.1074e-050.00636642intron-variantE4F1GRCh38.p716:2232378CGGTGAGCCGGCGTG[C/G/T]GGGGAGCCAGTGTGT1877
rs374336568snpA/Gintron-variantE4F1GRCh38.p716:2230179CCCTCTGGTGTGGGA[A/G]TGGTGATTGCTACAC1877
rs374373444snpC/T0.0002029990.0100727intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234998CCAGGAGTATATCAT[C/T]GAGGTGGGTGTGGGG1877
rs374483220snpA/Gintron-variantE4F1GRCh38.p716:2227903TCCTGGGCTCAAGCT[A/G]TCCTCCCACCTTGGC1877
rs374527304snpC/T5.02449e-050.00501198missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234290GGCGACTGCGGGAAG[C/T]TCTACAAGACCATTG1877
rs374607484snpA/Gupstream-variant-2KBE4F1GRCh38.p716:2221629GAACTCCTGATGTCA[A/G]GTGATCCACCCACCT1877
rs374662668snpA/G0.009934190.0697739intron-variantE4F1GRCh38.p716:2230349GATGCTTGTGCAGGG[A/G]GGCATTCAGAGGCAG1877
rs374688881snpC/T0.0001539880.00877327missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235104GGACGATGCGGAGAC[C/T]AGTGAGGCCACGGAG1877
rs374700250snpG/T0.0001044880.00722724missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234924GCGGCAGCCACCACC[G/T]TCCTCACGGAAGACC1877
rs374841967snpA/C/G6.37681e-050.00564623missense, synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2223624GCGACATGGAGGGCG[A/C/G]GATGGCAGTGCGGGT1877
rs374882960snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2222855GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA1877
rs374926049snpC/T0.001047630.022863intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235066TGACCTCTGTCCTTC[C/T]GCCCATCTGCCCAGG1877
rs374927912snpC/T5.05753e-050.00502843utr-variant-5-prime, missense, nc-transcript-variantE4F1GRCh38.p716:2223575GTTGTTATGACGACA[C/T]GGTCGTAAATCCGCC1877
rs374937976snpC/G1.66868e-050.00288845intron-variantE4F1GRCh38.p716:2229544AGCATACAGACGACT[C/G]CCCTGTTTTCTTCCC1877
rs374953286snpA/C/T0.001050420.0228947missense, synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233126GGGCACCGTCATCCA[A/C/T]GAAGTCCACGTCCAG1877
rs374969325snpA/G0.002791620.0372561intron-variantE4F1GRCh38.p716:2233814AGGGTGGGGCCCATG[A/G]TTGTGTTCTTGGTAC1877
rs375039813snpA/G0.0003231020.0127062missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233576CCAGCTCCTGCTGCC[A/G]GGTCCAGTCCCCAGC1877
rs375148567snpA/G5.311e-050.00515288intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235204CGCTCTTGCTGAGCC[A/G]TGGCCCTGCAGGTGG1877
rs375170561snpC/T8.58369e-050.00655066missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234649TGCCAGTTCTGCAGC[C/T]GTGGCTTCCGAGAGA1877
rs375178489snpC/T0.0001184680.00769546synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232223GGCGGAGCTGGGAGA[C/T]GGTGAGATGGCCGAG1877
rs375194455snpC/G/T3.31985e-050.00407411missense, nc-transcript-variantE4F1GRCh38.p716:2232833CGGCACCTCAAGTCT[C/G/T]TCACCCCCTGCACAG1877
rs375309480snpC/G/T3.33975e-050.0040863missense, nc-transcript-variantE4F1GRCh38.p716:2233026GTTCTGGAGCTGGAG[C/G/T]TGCCGGCTTGGGGAC1877
rs375358824snpA/G0.0001539880.00877328missense, nc-transcript-variantE4F1GRCh38.p716:2228425GAGTTCACCGCCTTG[A/G]AGGATTTTGTTCAGC1877
rs375397955snpA/Gupstream-variant-2KBE4F1GRCh38.p716:2222206TAGCCTAGGTGACAG[A/G]GCGAGACTCCATCTC1877
rs375407226snpC/G0.0001735690.0093142intron-variant, missenseE4F1GRCh38.p716:2228365GCTGACAGCAGGCTC[C/G]TTGCAGATGAGGACG1877
rs375530655snpC/Tintron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223867CGGGCTCGACCGACC[C/T]TCCCAGACCCAGACA1877
rs375602180snpA/G0.003587790.0422022intron-variantE4F1GRCh38.p716:2233364CACAAGGCTCCTGGC[A/G]TGCGTCTGCCCCATG1877
rs375723167snpA/G0.0001061870.00728576intron-variantE4F1GRCh38.p716:2232607CTCGGGCTGGAGCCC[A/G]GTAGCACCCCGATGG1877
rs376064191snpC/G0.0007925750.0198912intron-variantE4F1GRCh38.p716:2228542AGCCCTCACCCACTC[C/G]CCCATCCCCTCCCGG1877
rs376235056snpC/Gmissense, nc-transcript-variantE4F1GRCh38.p716:2229675GCATCTGACCTTGTT[C/G]GTAAGCCGACTTCCA1877
rs376359524in-del-/Gframeshift-variant, nc-transcript-variantE4F1GRCh38.p716:2223708GGGTGCAGTTGCGGC[-/G]GGTGGCGGCGGCCTT1877
rs376712603snpC/Gintron-variantE4F1GRCh38.p716:2226920CAGCTCCCTGCATTT[C/G]CCTCTCAGCCAGAGC1877
rs376798905snpC/Tintron-variantE4F1GRCh38.p716:2234075TCCAGGGTGGGTCCA[C/T]AGACAGCAGGGAGCC1877
rs376804356snpA/C/T0.0001224010.00782221utr-variant-3-prime, missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235266CGTGCACCAGGCTAG[A/C/T]GCCGGCCACCAGATC1877
rs376901022snpC/G1.66988e-050.00288949intron-variantE4F1GRCh38.p716:2229688TTGGTAAGCCGACTT[C/G]CATGAATCGCTGGCC1877
rs377092233snpA/G/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229391GATTGGACTGGGACC[A/G/T]GTGGTCGTGTTGGGG1877
rs377234026snpC/T0.003730280.0430258intron-variantE4F1GRCh38.p716:2233850GGGCACAGCCTGCCC[C/T]GGGTGCTGGAGACCT1877
rs377249962snpC/G/T0.001211320.0245829intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234415GCCGCAGGACCCTGG[C/G/T]GCCTGATCCCCCCAT1877
rs377282911snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225374CACTGTGGCTCATAC[C/G]TGTAACCCCAACACT1877
rs377409835snpC/T2.25309e-050.00335633missense, synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2223669CGGCAGAAGCCCAGG[C/T]CGAAGCCGGGCGGGA1877
rs377473883snpC/T0.0001129110.00751285synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234750TGGCTTCGCCGAGCA[C/T]GGCACGCTGAACCGG1877
rs377483446snpC/Tintron-variantE4F1GRCh38.p716:2226504ATAGCTGTGGTTTGG[C/T]CCTTTCTCCGCCCTC1877
rs377572921snpA/G0.0001915730.00978517utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235314CATGGACGAGGAGAC[A/G]GCGCTGGGCCCAGAG1877
rs377655467snpA/C/G4.98893e-050.00499425synonymous-codon, missense, nc-transcript-variantE4F1GRCh38.p716:2232895GGTTGTCAGCAAAGA[A/C/G]GACGCACGTGCAGGT1877
rs527240399snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226053AGCTGAGATCGCCCC[A/G]CTGCACTCCAGCCTG1877
rs527420469snpC/T0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235962CTGGAGCTGTGCCCC[C/T]AGCTGCGCTGCCTGA1877
rs527623336snpA/G0.0007984030.0199641intron-variantE4F1GRCh38.p716:2226581GGGTTTGATCCTGCC[A/G]AGGGACTGAAGGTGA1877
rs527754725snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225338CTCTGAGCTTGTCCT[A/G]TGAGGCTGCAGATGG1877
rs527815095snpC/Tintron-variantE4F1GRCh38.p716:2225627TACGGCACGCGGCAT[C/T]ACACCCGGCTAATTT1877
rs527879308snpA/G0.0003992810.0141238utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235678GCACAGGATGGAGGC[A/G]CCCCAAGACGGACAG1877
rs528154117snpC/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222164GAGGCGGAGATTGCA[C/G]TGAACCAAGATCGTG1877
rs528212883snpC/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2221553CGTGCACCACCACAC[C/G]CAGATAATTTTTGTA1877
rs528618207snpC/T0.00239330.0345097intron-variantE4F1GRCh38.p716:2227815CTAAATGTTTAACAA[C/T]GTTTTAAAAACTTTT1877
rs528770998snpA/Gintron-variantE4F1GRCh38.p716:2231559TGAACTGTGTTTACA[A/G]CCTAGCTTTGCACAT1877
rs528812715snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2232750CTGACTAGGTTCTCT[C/T]TGCAGATGAGCGCCC1877
rs528812934snpC/Tmissense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233646TGCAGCCGCTGGAGA[C/T]AGTAGGTGCCAGCAC1877
rs529037675snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225386TACCTGTAACCCCAA[C/G]ACTTTGGGAGGCTGA1877
rs529097249snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230447TAGGTGTGCAGACGC[A/G]AGGGAAGGAGCTGTC1877
rs529237766snpA/G0.0001039080.00720716utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235516CTGGAGCATGCAGGC[A/G]AGCTGGTCATCGCCT1877
rs529305808snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228997GAACCCCGCACACGC[C/T]GCAGCGGGCGCTTGT1877
rs529404877snpA/C/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231204CAGGTCCTGTCTTTG[A/C/T]GGGTGCAGGGGTGCG1877
rs529417951snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2234041GATGGGCTATAGGTG[C/G]CCGGGGTGCTTCTGG1877
rs529658042snpA/G/T4.49691e-050.00474157missense, synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2223744CCAGCGGCTTCCTCG[A/G/T]CCTCCCGGCGCCCTT1877
rs529675186snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226669GTAAACAGGTACTGT[C/T]CCTGACACTCAGCCG1877
rs529712952snpC/T1.82673e-050.00302214synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232530GCTCTGTGGGGCCTC[C/T]TTCCGCACCAAGGGC1877
rs529907238snpA/G0.00110010.0234273utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235270CACCAGGCTAGCGCC[A/G]GCCACCAGATCATCG1877
rs530255666snpA/G0.0007984030.0199641intron-variantE4F1GRCh38.p716:2225847GCGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG1877
rs530565857snpA/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222947GAATGGCGTGAACCC[A/G]GGAGGCAGAGCTTGC1877
rs530921933snpA/G1.71281e-050.00292639missense, nc-transcript-variantE4F1GRCh38.p716:2233169TCCCTGGGCATGAAA[A/G]CCCTGGCCCCAGAGG1877
rs531092764snpA/G0.0007984030.0199641upstream-variant-2KBE4F1GRCh38.p716:2222240AAACAAAAACAGGCC[A/G]GGCGCGGTGGCTCAT1877
rs531141181snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227959GTGAGCCACCATGCC[C/T]GGCCCCAGCAGTCTT1877
rs531154006snpC/T0.0001360750.00824737missense, nc-transcript-variantE4F1GRCh38.p716:2228474GCCAGCGGGCCCCTC[C/T]GGAGGCCCTGCCTGC1877
rs531263988snpA/C/T4.86784e-050.00493324missense, nc-transcript-variantE4F1GRCh38.p716:2233480TCCAGCGAGGGCAGC[A/C/T]GTGAGAACCTGCTGC1877
rs531343828snpC/T7.32681e-050.00605216utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235596CTGCGGGGTCCTGGC[C/T]GGGCAGGGACAGGGC1877
rs531567346snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224489AATCGAAGGTTGGAG[A/G]CCTGAAAGTGACCGG1877
rs531619455snpA/G0.001596170.0282053intron-variantE4F1GRCh38.p716:2229787CCAGGGCCTGGCTGG[A/G]AGGGGCCGCGGCCTC1877
rs531668569snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225496TTTTTTTTTTGAGAC[A/G]GCGTTTCTCTCTTGT1877
rs531872577in-del-/T0.2863030.24735intron-variantE4F1GRCh38.p716:2227827CAATGTTTTAAAAAC[-/T]TTTTTTTTTTTTTTT1877
rs532002945snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227673CACCGCCCTAATTTT[A/G]TATTTTTAGTAGAGA1877
rs532583403snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2232010ACCTGGAGAGGTGAA[C/T]GGGACCTTGGCTGTT1877
rs532913024snpA/G0.001197370.0244387intron-variantE4F1GRCh38.p716:2229868CTGGGCCTTCCTCAG[A/G]TGTCCACAGTGGCCG1877
rs532973687snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229495AGCTTTACACTGGCA[A/G]AGCCCAGGCCTCTTC1877
rs532995496snpA/G/T5.26607e-050.00513104utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235239CCACATCATGAAGGT[A/G/T]GTGCAGCAGATCGTG1877
rs533083336snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2231664GAGAGCGTTCACTCT[C/T]CCAGGCCAAGCCTGC1877
rs533127513snpC/T0.0001189180.00771004synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233917AGCGGTGCCCAGGAC[C/T]CACCCATGTCCTCAG1877
rs533250705snpC/Tintron-variant, missenseE4F1GRCh38.p716:2228362CCTGCTGACAGCAGG[C/T]TCGTTGCAGATGAGG1877
rs533283493snpA/G0.004877280.0491411intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234791CCAAAGGTCTGGGCC[A/G]GTGGAGGTGGGAGGG1877
rs533310718snpA/T0.008747350.0655527intron-variantE4F1GRCh38.p716:2225825AAAAGGCTGGGCGCA[A/T]TGGCTCGCGCCTGTA1877
rs533493160snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222467GCTGCAGTGAGATCG[C/T]GCCATTGCACTCCAG1877
rs533708644snpC/T0.003189780.0398085intron-variantE4F1GRCh38.p716:2228935ATCAGCAAATGGCCA[C/T]CTTTGCTGAGCCCCA1877
rs533903373snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224975CCCAGCACTTTGGGA[A/G]GCCAAGGTGGGTGGA1877
rs533919214snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230645AGGGGGTGGAGGAGC[C/T]GTGGCGGAGGCCAAC1877
rs534584392snpC/T6.76224e-050.00581435intron-variantE4F1GRCh38.p716:2232956GGGGCTGGCTGTGGA[C/T]GCAGCCGCCACTGGG1877
rs534689979snpC/G0.001197370.0244387intron-variantE4F1GRCh38.p716:2226361TTCAGTGGCAATGCC[C/G]TGGAGCCGAGTGAGA1877
rs534774309snpC/T0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236153TCAGGGAGGCAGAGT[C/T]TAGGCGACCTAATTT1877
rs534808087snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2221764GGAGTTCTATAGCAG[C/T]CTAGGCAACATGGCA1877
rs534812287snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228167GAGGGTGGGTCTGGC[C/T]CCTGCAGACCTGCAG1877
rs534827168snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2233318AGGGAGAGCAGGGCC[A/G]GTGGGAGCGCCATGG1877
rs535007953snpA/G3.49852e-050.00418227intron-variantE4F1GRCh38.p716:2232133GGGTCTCTGGACAGG[A/G]GCAGGTCCTGGGGCT1877
rs535013880snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226823TCTCTTCTGCACGAC[C/T]GGGGTCCGGCACAGC1877
rs535391582snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2223982CCTGTCATCCCCCCT[C/T]TCTGGTGTGCGTCCA1877
rs535438537snpC/T0.001197370.0244387intron-variantE4F1GRCh38.p716:2229208GCCCTCTCCTCACAC[C/T]GCTCTGCCGGATGTG1877
rs535609007snpC/T4.0312e-050.00448936intron-variantE4F1GRCh38.p716:2228565CCTCCCGGGTTCACC[C/T]GACAGGTGGGGGAGG1877
rs535658342snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224676GCGGGCGCCTGTAGT[C/G]GGGAGGCTGAGGCGG1877
rs535759108snpC/Tintron-variantE4F1GRCh38.p716:2229796GGCTGGGAGGGGCCG[C/T]GGCCTCGTGGCAGCC1877
rs535986793snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2221873AGAGGCTGCAGTGAG[C/T]TGAGATCACGGCACT1877
rs536442670snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225686CATGTTGGCCAGGCT[A/G]GTCTTGAACTCCCGA1877
rs536454671snpG/T0.001197370.0244387intron-variantE4F1GRCh38.p716:2230809ATGTTCATGTGGGAG[G/T]TGGGGCGGGCTCTGG1877
rs536516786snpA/G0.0003992810.0141238utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235730GCTTTACAATAAAAC[A/G]TGAGAACCTGCAGCT1877
rs536833832snpA/Cintron-variantE4F1GRCh38.p716:2231371TCACTCCTGGGGCAT[A/C]GAGCGTGTAAGGGCT1877
rs536849171snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231299CGTCTCCTCTGGCCT[C/T]GCAGCAGCCATGTTC1877
rs536922221snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2233669GCCAGCACCACCTGC[A/G]GGCTCCTCCCAGGGC1877
rs536925571snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2230273GAAGATGTCTCTCTC[C/T]CTGATGTGCTGTGGG1877
rs537259861snpC/T0.002791620.0372561intron-variantE4F1GRCh38.p716:2228632CGGGGGCCACGTGGG[C/T]GGGCAGAGGGCAGGC1877
rs537267947snpG/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2221607CCATGTTGGCCTGCT[G/T]GGTCTTGAACTCCTG1877
rs537401958snpC/Gintron-variantE4F1GRCh38.p716:2224079GCCCTTCTCTGCCTC[C/G]GATGCCTGAGCCTGG1877
rs537442534snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224778GCAGAGCCGGACTCC[C/G]TCTCAAAAGAAAAGA1877
rs537451589snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227465CAAGCTCTGCCTGCC[C/G]GGTTCATGCCATTCT1877
rs537851333snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230096TGGGTACAGGGTGGA[C/T]GGGACTCTCCCGCCT1877
rs537862010snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224210GCTCTGGGCCTGTCC[C/G]TAGGGAGGCAGCAGA1877
rs537873850snpC/T0.006369360.0560724upstream-variant-2KBE4F1GRCh38.p716:2223095TACCCATGAGCCATC[C/T]CCGACCCGTGTTCTT1877
rs537989253snpC/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2223295CCAGTCCGCTCGCCC[C/G]TCGCGTTCTCTGGCT1877
rs538365814snpC/Gintron-variantE4F1GRCh38.p716:2224503GACCTGAAAGTGACC[C/G]GGTGGGCTGGGTGCG1877
rs538432324snpC/G2.13018e-050.0032635intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235013CGAGGTGGGTGTGGG[C/G]CCCTGGGGCCGTGCT1877
rs538648342snpC/T0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235774CAGTGGCAGCCTCCG[C/T]GGCTGGTGCCACCAC1877
rs538862711snpA/C0.001197370.0244387intron-variantE4F1GRCh38.p716:2226213TGCCTTTTTTCCTTG[A/C]CCCTTCTCGTTCCAG1877
rs538906906snpA/Gupstream-variant-2KBE4F1GRCh38.p716:2221546TTACACGCGTGCACC[A/G]CCACACCCAGATAAT1877
rs539015855snpG/T0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236080CAGCAGGAGATGCTG[G/T]GTAGGGAGTGTGGCT1877
rs539057194snpC/T0.0001849250.00961396intron-variantE4F1GRCh38.p716:2234156GGCTTGGCCTGATGC[C/T]GTGTGTGGCTGCAGG1877
rs539199880snpG/T0.0003143170.0125323intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223822GGGCAGTTCATCCCG[G/T]GCTGGCAGAGGCCCG1877
rs539378764snpC/T0.008351410.0640778intron-variantE4F1GRCh38.p716:2229183AAGGCCTCTGGCCCA[C/T]ACCTCCAGGGCCCTC1877
rs539424232snpA/G0.0007984030.0199641intron-variantE4F1GRCh38.p716:2233787TTCCCTGGGGCCACA[A/G]GGGAGCCTGCCAGGG1877
rs539773841snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2221753GCTTGAACTCAGGAG[C/T]TCTATAGCAGCCTAG1877
rs539854524snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228100AGCCTTAGCAGGTCC[C/T]TGCAGCCTAAGCGTG1877
rs539965437snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227497CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAT1877
rs539965441snpA/G0.001197370.0244387intron-variantE4F1GRCh38.p716:2233255GTCTTTGTTCTGGGC[A/G]CTGGCTCCAGGGGTC1877
rs540038120snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230416TGGGGTTGGGGGTGC[A/G]GCAGGGGCGAGTGGC1877
rs540243236snpA/G0.0003992810.0141238intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234519CCTTGGGCCACAGGC[A/G]GGAGGGGAGAGCTGT1877
rs540405594snpC/T0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235843CCACTCCTAGACTCA[C/T]GTGCCTGGCCGCCCC1877
rs540461168snpA/Gupstream-variant-2KBE4F1GRCh38.p716:2222614GCCTGTCATCCTAGC[A/G]CTTTGGGAGGCCGAA1877
rs540714147snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231940ATTTAGGGGCCCTGG[A/G]GCATCTCTGGGCAGC1877
rs540780876snpA/G1.73192e-050.00294267synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235126GCCACGGAGATCATC[A/G]AGGGCACCCAGACAG1877
rs540822546snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224305GCTTTCTAGTTCTTT[A/G]ATCCTGGGTAGGTGA1877
rs540895897snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229347GAGGTGTGAGAGTGA[C/T]GGCGCTGACCCTGGC1877
rs541004611snpA/G2.06969e-050.00321683intron-variantE4F1GRCh38.p716:2232434CCAGGAGGGCCCTGA[A/G]CTGCCACGCCCTCCC1877
rs541095921snpA/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225368GCTGGGCACTGTGGC[A/T]CATACCTGTAACCCC1877
rs541204253snpC/T0.01269790.078662downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235884TTCTGCCAGCCCTGG[C/T]GGCGCCTTGGTGCTG1877
rs541301791snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227009ACATGCTCCAGGGCA[C/T]GCTCAAACTCCCGCA1877
rs541486521snpG/T0.001596170.0282053intron-variantE4F1GRCh38.p716:2231005TCAGCAGCCCCTCTT[G/T]GCACCCCTGCCACTC1877
rs541498247snpC/T0.0007984030.0199641upstream-variant-2KBE4F1GRCh38.p716:2222176GCAGTGAACCAAGAT[C/T]GTGCCGTTGCATTCT1877
rs541525310snpC/Tintron-variantE4F1GRCh38.p716:2227697GTAGAGATGGGATTT[C/T]ACCATATTGGTCAGG1877
rs541530140snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228808TGGAGGGTCTCCTTT[A/G]GCTCTGGGGTACCAT1877
rs542125740snpG/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227520GGGACTATAGGCACC[G/T]GCCACCATGCCTGGC1877
rs542286926snpC/Tintron-variantE4F1GRCh38.p716:2224723GGGAGGTGGAGCTTG[C/T]GGTGAGCCGAGACCG1877
rs542396099snpA/G3.38587e-050.00411439missense, nc-transcript-variantE4F1GRCh38.p716:2228465AGAAGGCCTGCCAGC[A/G]GGCCCCTCCGGAGGC1877
rs542505220snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231094GCCAGTCAGCAGGCC[C/T]GGTGGGCTTAGTCCA1877
rs542642756snpA/C0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229778CTCCCGAGACCAGGG[A/C]CTGGCTGGGAGGGGC1877
rs542672426snpA/G0.0003992810.0141238missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234745GGCCGTGGCTTCGCC[A/G]AGCACGGCACGCTGA1877
rs542924573snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224410TCCTGCTTTAGGTTT[C/T]TTCATTCTCAAACCA1877
rs542965861snpA/G5.59362e-050.00528819utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235567GTGCAGACGGTCATC[A/G]TCTAGCATGAGGTCT1877
rs543017512snpA/G/T0.0008041650.0200383synonymous-codon, missense, nc-transcript-variantE4F1GRCh38.p716:2233036TGGAGCTGCCGGCTT[A/G/T]GGGACAGCCACATCA1877
rs543079123snpC/T0.0001815440.00952571missense, nc-transcript-variantE4F1GRCh38.p716:2232534TGTGGGGCCTCCTTC[C/T]GCACCAAGGGCTCAC1877
rs543217345snpA/G0.001197370.0244387intron-variantE4F1GRCh38.p716:2225154GGAGACGGAGGTCGC[A/G]GTAAGCCGAGATCGC1877
rs543263895snpA/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222014CACCTGAGGTCAGGA[A/G]TTCAAAACCAGCATG1877
rs543477747snpC/Tintron-variantE4F1GRCh38.p716:2230821GAGGTGGGGCGGGCT[C/T]TGGCCTTGACCTGGC1877
rs543683068snpC/T0.0006033840.0173588synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233890TCCCCAGCAGGTGGC[C/T]AGCGAGGCCTCAGCG1877
rs543875333snpC/T0.0002660680.011531synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232898TGTCAGCAAAGAGGA[C/T]GCACGTGCAGGTCAG1877
rs543919639snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2222047CAACATGGTGAAACT[C/T]CGTCTCTCCTAAAAA1877
rs543978808snpC/T1.77184e-050.00297639intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235203CCGCTCTTGCTGAGC[C/T]GTGGCCCTGCAGGTG1877
rs544001737snpC/G/T0.0003992810.0141238utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantE4F1GRCh38.p716:2223549CCCTCACGCTGGCCT[C/G/T]GGCGCGGCCCGTTGT1877
rs544741282in-del-/Tintron-variantE4F1GRCh38.p716:2227827AATGTTTTAAAAACT[-/T]TTTTTTTTTTTTTTT1877
rs544779797snpC/T0.001197370.0244387upstream-variant-2KBE4F1GRCh38.p716:2223003CTCCAGCCTGGGCGA[C/T]AGAAAGAGACTCCGT1877
rs544810298snpA/G0.0007984030.0199641intron-variantE4F1GRCh38.p716:2229283CCTGCCAGAGTTGCT[A/G]CTCCCTCCCTGCAGG1877
rs544822081snpA/G0.0007984030.0199641intron-variantE4F1GRCh38.p716:2228887CTAGGGACTTCACAC[A/G]TGAAGTGTGGCCCTG1877
rs544883555snpC/G/T0.00015620.00883627missense, synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233893CCAGCAGGTGGCCAG[C/G/T]GAGGCCTCAGCGGTG1877
rs545002319snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230324GATGGGCAGGCTCTC[A/G]TCGGGGACAGATGCT1877
rs545063260snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229828TTCTGCGGGCACAGC[C/T]TGCAGGAGGAGGAAG1877
rs545228886snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226552TTTGCCCAGCTCCTT[C/T]GGGCATCAGGCCTGG1877
rs545292189snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2231865TCACCAGGATTCGCA[C/T]GTCCTCCTGGCTTTG1877
rs545385916snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222084AAAATTAGCCGGGTG[C/T]GGTGGCAGTTGCCTG1877
rs545548940snpA/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2233393TGGGGTGGGTGCTGG[A/T]TGCCAGGCTGCCTGG1877
rs545657039snpC/T0.0002151690.0103701intron-variantE4F1GRCh38.p716:2233674CACCACCTGCGGGCT[C/T]CTCCCAGGGCTGGAT1877
rs545712149snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225755GGGAATACAGTCGTG[C/T]GCCACCGTGCCCGGC1877
rs545721478snpA/G0.001197370.0244387upstream-variant-2KBE4F1GRCh38.p716:2222786CCAGCACTTTGGGAG[A/G]CCGAGGCGGGCGGAT1877
rs546090889snpG/Tupstream-variant-2KBE4F1GRCh38.p716:2222879TACAAAAAATTAGCC[G/T]GGCGTGGTGGCGGAC1877
rs546127483snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2224539TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGT1877
rs546435455snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2223966CCTCTCCTGCGGGGC[C/G]CCTGTCATCCCCCCT1877
rs546597815snpC/T0.0003992810.0141238intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234842TTGCCTAGCCCTGAC[C/T]GAGTCCCCACCCACA1877
rs546817911snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229894GGCCGGGGGCACACC[C/T]AGGCACCAGGGAGTC1877
rs547092769snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2233284TCTGAGCCAGGCAGG[C/T]GAGGGCTGGGCTTCC1877
rs547108944snpC/Tintron-variantE4F1GRCh38.p716:2231582TTGCACATTGTCAGA[C/T]TTTTCCCAGCATCCT1877
rs547365145snpC/T0.001994810.0315187intron-variantE4F1GRCh38.p716:2229390GGATTGGACTGGGAC[C/T]GGTGGTCGTGTTGGG1877
rs547398500snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226615GTCAGAGCTGGCAGG[C/T]TTTTATGGAAGCAGA1877
rs547548045snpC/Gintron-variantE4F1GRCh38.p716:2225663TTTTAGTAGAGACTG[C/G]ATTTCTCCATGTTGG1877
rs548007057snpG/Tupstream-variant-2KBE4F1GRCh38.p716:2223372CCCCCTGGCTGGCAA[G/T]CTGCTCCACCGTAAC1877
rs548196162snpA/Gintron-variantE4F1GRCh38.p716:2226458CCATCAGGAGAGGAC[A/G]ACTCTGTTGGGTGGC1877
rs548400100snpA/G0.003735310.0430547missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233630CTGCCGGTACTGGAA[A/G]TGCAGCCGCTGGAGA1877
rs548678614snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229967TGCCGTGTCCCTCCC[A/G]GAATCTTCCCCACTT1877
rs548701625snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2223102GAGCCATCCCCGACC[C/T]GTGTTCTTTTCCCGT1877
rs548826122snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2227410GGAGTCTCGCTCTTT[C/T]GCCCAGGCTGGAGTG1877
rs549051976snpA/G0.0003992810.0141238intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234965GTTGGTGGAGTTCTC[A/G]TCCGTGGTAGCTGAC1877
rs549167809snpC/T0.001197370.0244387intron-variantE4F1GRCh38.p716:2229006ACACGCCGCAGCGGG[C/T]GCTTGTCATCCGCAT1877
rs549208955snpA/G0.0007984030.0199641intron-variantE4F1GRCh38.p716:2225394ACCCCAACACTTTGG[A/G]AGGCTGAGGTGAGAG1877
rs549376301snpC/Tintron-variantE4F1GRCh38.p716:2228748TTGGCAGCCTCTGGT[C/T]GAAGCCCGTGCTGTT1877
rs549478822snpC/G0.0007984030.0199641intron-variantE4F1GRCh38.p716:2228584AGGTGGGGGAGGTGG[C/G]CGCGCTTCAGGATGG1877
rs549813797snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226684CCCTGACACTCAGCC[A/G]TTTGGTGACCTTGAA1877
rs549818352snpC/Tutr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantE4F1GRCh38.p716:2223522GTTCTGCCCCGCCCT[C/T]CTCTTGCCGTTCCCT1877
rs549869922snpC/Tintron-variantE4F1GRCh38.p716:2231762AAGAGTGGCCCCGGA[C/T]GCACATCCTCCCTAT1877
rs549906446snpC/T0.001994810.0315187intron-variantE4F1GRCh38.p716:2234079GGGTGGGTCCATAGA[C/T]AGCAGGGAGCCAGGG1877
rs549939621snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231972TGACAGAGTCGGGAG[C/G]TGTCTCTCCACCTCT1877
rs550016838snpC/T0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236036TCTGGGAGCCTCGGC[C/T]TCCACCGCAGGGTGA1877
rs550028886snpC/Gintron-variant, synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2223808TGCGGCCGGGGTGCG[C/G]GCAGTTCATCCCGGG1877
rs550065657snpA/T0.01230360.0774623intron-variantE4F1GRCh38.p716:2225851CTGTAATCCCAGCAC[A/T]TTGGGAGGCTGAGAC1877
rs550403405snpC/T0.0003992810.0141238synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234774GAACCGGCACCTGCG[C/T]ACCAAAGGTCTGGGC1877
rs550405043snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229081GGCCACCAGTGGGCC[A/G]TGGCCCAGATGATGC1877
rs550896014snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222283AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCG1877
rs550928091snpA/C0.0007984030.0199641intron-variantE4F1GRCh38.p716:2228039CCTCCCAGCCCCTCT[A/C]TGGGCCTCTCGCCTG1877
rs551031835snpA/C/G0.0001079130.00734478intron-variantE4F1GRCh38.p716:2233195AGAGGTGGGGGCGAC[A/C/G]GGGGGCCCCGGAGGG1877
rs551204352snpC/T0.0004823020.0155215utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235324GAGACGGCGCTGGGC[C/T]CAGAGGCGGCTGCCG1877
rs551377487snpC/T0.001596170.0282053intron-variantE4F1GRCh38.p716:2231184GGCCAAGGGCTGGGG[C/T]GTGCCAGGTCCTGTC1877
rs551377575snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2225559GCTCACCGCAACCTC[C/T]GCCTCCCGGGTTCAA1877
rs551551480snpG/T0.0001248360.00789952intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223807GTGCGGCCGGGGTGC[G/T]GGCAGTTCATCCCGG1877
rs551891208snpA/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2221537TAGCTAGGATTACAC[A/G]CGTGCACCACCACAC1877
rs552331332snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227179CTACAGGTGCATGCC[A/G]CCACACTTCCACGCT1877
rs552394617snpA/G0.001994810.0315187intron-variantE4F1GRCh38.p716:2232694CCCCTGCCTGCCTTC[A/G]CCTTGTCACCTTGTC1877
rs552396437snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2226753ATTTCCACAGGGTGC[C/T]GGCAAGATTTGGTGA1877
rs552806071snpC/T0.0007984030.0199641upstream-variant-2KBE4F1GRCh38.p716:2223462CCCTTTAAGGCCACA[C/T]CGCTATCCAGGCCCG1877
rs552871906snpA/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222799AGGCCGAGGCGGGCG[A/G]ATCACGAGGTCAGGA1877
rs552965184snpC/T1.75807e-050.0029648missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2234180CTGCAGGGCCGAGGC[C/T]GTTCGCCTGCGCGCA1877
rs553545176snpC/Tintron-variantE4F1GRCh38.p716:2226715CTTCAGGTCATTTTC[C/T]TAGGATGGGAATAGT1877
rs553821423snpC/T0.001197370.0244387intron-variantE4F1GRCh38.p716:2225877GAGACGGGCGGATCC[C/T]GAGGTCAGGAGATCG1877
rs553862865snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225614GAGTAGCTGGGATTA[C/T]GGCACGCGGCATCAC1877
rs553931948snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225078ATTAGCTGGGCGTGG[C/T]GGTGCGCGTCTGTAA1877
rs553953216snpC/Gintron-variantE4F1GRCh38.p716:2224385CTGCCAGTAATGTAA[C/G]AAGCCCTTATCCTGC1877
rs554133139snpA/Gintron-variantE4F1GRCh38.p716:2224186GGCCTCGGTTTCTCC[A/G]GGATCTGGGCTCTGG1877
rs554167134snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229767TATGCTCGTCTCTCC[C/T]GAGACCAGGGCCTGG1877
rs554382647snpC/T0.001197370.0244387intron-variantE4F1GRCh38.p716:2230199GATTGCTACACTGGT[C/T]CTCATGGGGCTTTTA1877
rs554413751snpC/Tintron-variantE4F1GRCh38.p716:2229555GACTCCCCTGTTTTC[C/T]TCCCCCTTTGGCAGG1877
rs554506593snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228177CTGGCCCCTGCAGAC[C/T]TGCAGAGGATAGGGG1877
rs554520634snpC/T0.001197370.0244387intron-variantE4F1GRCh38.p716:2233326CAGGGCCAGTGGGAG[C/T]GCCATGGGGGTCTGA1877
rs554801748snpG/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227585CACGGTGTTAGCCAG[G/T]ATGGTCTCAATCTCC1877
rs554879081snpA/C0.004780850.0486577intron-variantE4F1GRCh38.p716:2231504CTAAGCAGTGGCTTC[A/C]CAGCTGTTTCCCACT1877
rs554915155snpC/T0.0002667350.0115454intron-variantE4F1GRCh38.p716:2232441GGCCCTGAGCTGCCA[C/T]GCCCTCCCCCACAGG1877
rs554985849snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226847GCACAGCAATGGTGA[C/T]GGGCTCAACCTTGGG1877
rs555106916snpC/G0.0003992810.0141238utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantE4F1GRCh38.p716:2223510CAATCCGCTCCGGTT[C/G]TGCCCCGCCCTCCTC1877
rs555109925snpA/C0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236160GGCAGAGTCTAGGCG[A/C]CCTAATTTCTAGGGG1877
rs555119381snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229216CTCACACCGCTCTGC[C/T]GGATGTGGCGGGCTG1877
rs555318087snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224038CCGGGCGCCCGGTGT[A/G]GACATTCGCAGACGC1877
rs555333337snpC/Tintron-variantE4F1GRCh38.p716:2230068CCACTCGCCCAGCAG[C/T]GGCTCTGGAGGGTGG1877
rs555859013snpA/G0.001197370.0244387upstream-variant-2KBE4F1GRCh38.p716:2222627GCACTTTGGGAGGCC[A/G]AAATGGGAAAATGGT1877
rs556381523snpA/Gintron-variantE4F1GRCh38.p716:2227411GAGTCTCGCTCTTTC[A/G]CCCAGGCTGGAGTGC1877
rs556467331in-del-/AG0.001197370.0244387intron-variantE4F1GRCh38.p716:2230784TCATCAATGCCACTC[-/AG]AGCTCGGAATGTTCA1877
rs556531199snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225167GCAGTAAGCCGAGAT[C/T]GCACCACTGCTCTCC1877
rs556568778snpC/T0.001197370.0244387intron-variantE4F1GRCh38.p716:2233363GCACAAGGCTCCTGG[C/T]GTGCGTCTGCCCCAT1877
rs556768542snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230837TGGCCTTGACCTGGC[A/G]TTTGGTTTCTGGGAT1877
rs556792905snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228657GCAGGCACCTGGCTG[C/T]GGTGTGGGAGGGTCC1877
rs557380600snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226932TTTGCCTCTCAGCCA[C/G]AGCCAGTGGGCATCA1877
rs557523344snpA/C0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224235AGCAGAGCCTAGTGC[A/C]AGAGGGCTGGTGCAC1877
rs557778178snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224816CAGGGTCACCCAGGT[A/G]GTTAAGTAGCAAGGG1877
rs557840914snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230108GGACGGGACTCTCCC[A/G]CCTCTCTAGCTGGGC1877
rs558124807snpA/Gintron-variantE4F1GRCh38.p716:2230430CGGCAGGGGCGAGTG[A/G]CTAGGTGTGCAGACG1877
rs558160581snpC/Gupstream-variant-2KBE4F1GRCh38.p716:2221709CACAATTTTTTAAAA[C/G]TATGTAAGAGGGCTG1877
rs558422719snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2229288CAGAGTTGCTGCTCC[C/T]TCCCTGCAGGCGCCC1877
rs558486175snpA/G0.0003992810.0141238intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234445TCCTGCTCCCTGGCC[A/G]TGGCCCAGGTGCACC1877
rs558562765snpC/G0.001994810.0315187intron-variantE4F1GRCh38.p716:2230979CTAGGCTCAGCACCC[C/G]TCCCTGTGCTTCAGC1877
rs558716972snpC/G0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236108GCTGGTCCTACCTGC[C/G]CTGCCTTGCTTTCCC1877
rs558784921snpC/T0.004780850.0486577intron-variantE4F1GRCh38.p716:2226223CCTTGCCCCTTCTCG[C/T]TCCAGCTTGGAGAAG1877
rs558842274snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225761ACAGTCGTGCGCCAC[C/T]GTGCCCGGCTCCTCC1877
rs558844494snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231407AGGAGAGGCTCTTAA[C/T]TGTTTCTGAGTCACC1877
rs558958688snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222090AGCCGGGTGTGGTGG[C/T]AGTTGCCTGTAGTCC1877
rs559005242snpC/T0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235784CTCCGCGGCTGGTGC[C/T]ACCACCTTTGCCCAG1877
rs559020263snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2221547TACACGCGTGCACCA[C/T]CACACCCAGATAATT1877
rs559034112snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227766TCAGCCTCCCAAAGT[A/G]TTGGGATTACAGGTG1877
rs559838826in-del-/AA0.005575420.0525036intron-variantE4F1GRCh38.p716:2231462ACAGCTTGTCAAAAC[-/AA]GACGCCAGCCGGACT1877
rs560322571snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230435GGGGCGAGTGGCTAG[C/G]TGTGCAGACGCGAGG1877
rs560483622snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2228988CAGGCCTGTGAACCC[C/T]GCACACGCCGCAGCG1877
rs560766438snpC/T2.64253e-050.00363483missense, synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2223699AAGCGGGCGAGGGTG[C/T]AGTTGCGGCGGTGGC1877
rs560849176snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229351TGTGAGAGTGACGGC[A/G]CTGACCCTGGCCCGG1877
rs561026899snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231962CTGGGCAGCCTGACA[C/G]AGTCGGGAGGTGTCT1877
rs561042459snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227023ACGCTCAAACTCCCG[C/T]AGTTTTTGTTTGTTT1877
rs561775570snpA/G0.001994810.0315187upstream-variant-2KBE4F1GRCh38.p716:2222915TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG1877
rs561834662snpA/C0.001994810.0315187intron-variantE4F1GRCh38.p716:2228826TCTGGGGTACCATGG[A/C]AGCTTCTGTCTCTTT1877
rs561921813snpA/Gintron-variantE4F1GRCh38.p716:2225435GCCCAAGGAGTTCCA[A/G]ACCAGCCTGGGCAAC1877
rs562171322snpC/G0.0003992810.0141238missense, nc-transcript-variantE4F1GRCh38.p716:2228468AGGCCTGCCAGCGGG[C/G]CCCTCCGGAGGCCCT1877
rs562394148in-del-/A0.005972470.0543191intron-variantE4F1GRCh38.p716:2224632CTCTACTAAAAATAC[-/A]AAAAAAACAAAATTA1877
rs562722356snpA/Gintron-variantE4F1GRCh38.p716:2224660TTAGCCGGGCGTGGT[A/G]GCGGGCGCCTGTAGT1877
rs562762677snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231095CCAGTCAGCAGGCCC[A/G]GTGGGCTTAGTCCAG1877
rs562771864snpG/T0.008082310.0630542intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223794GCCGACCCGGAGGGT[G/T]CGGCCGGGGTGCGGG1877
rs562834928snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229389GGGATTGGACTGGGA[C/T]CGGTGGTCGTGTTGG1877
rs562884319snpC/Gupstream-variant-2KBE4F1GRCh38.p716:2223013GGCGATAGAAAGAGA[C/G]TCCGTCTCAAAAAAG1877
rs562930418snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229779TCCCGAGACCAGGGC[C/G]TGGCTGGGAGGGGCC1877
rs563392255snpG/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2227077GCAGGGTCTTGCCCT[G/T]TTGCCCTGGCTGAAG1877
rs563495207snpG/Tintron-variantE4F1GRCh38.p716:2226231CTTCTCGTTCCAGCT[G/T]GGAGAAGGGCAGTGC1877
rs563650627snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226484GTGGCCCCTGCAGGC[A/G]AGTCATAGCTGTGGT1877
rs564088935snpA/Cintron-variantE4F1GRCh38.p716:2233692CCCAGGGCTGGATCC[A/C]AGGGGCTGTCCCCAC1877
rs564228065snpA/G2.12407e-050.00325882synonymous-codon, missense, nc-transcript-variantE4F1GRCh38.p716:2223625CGACATGGAGGGCGC[A/G]ATGGCAGTGCGGGTG1877
rs564377166snpA/G0.001596170.0282053intron-variantE4F1GRCh38.p716:2228111GTCCCTGCAGCCTAA[A/G]CGTGCTGTCAGGGCC1877
rs564556685snpA/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2223050AAAAAAATTAAAAGT[A/G]TATAAAAGAATAAAA1877
rs564766796snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228902GTGAAGTGTGGCCCT[A/G]GGGGGTCCCGCCATC1877
rs564776934snpA/C6.87226e-050.00586145synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228499GCCTGCCACCCCTGC[A/C]ACCACAGCGTTGCTG1877
rs564887396snpC/Tintron-variantE4F1GRCh38.p716:2224456TGTTATTGTTATTCT[C/T]ATTTTGGGGATGAGG1877
rs564942581snpC/T0.005469320.0520072synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234585GGTGTCTCCACAGAA[C/T]GCACAGCAGGTGCAC1877
rs564972673snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225333GTACCCTCTGAGCTT[C/G]TCCTATGAGGCTGCA1877
rs564979481snpC/G0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235953CCTGCCCAGCTGGAG[C/G]TGTGCCCCCAGCTGC1877
rs565109546snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226966TCCTGGGCCCCAGCC[C/T]ATTTTACAGATGAGG1877
rs565177160snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226566TCGGGCATCAGGCCT[A/G]GGTTTGATCCTGCCG1877
rs565189658snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231871GGATTCGCACGTCCT[C/T]CTGGCTTTGGGGATG1877
rs565242919snpC/T1.73782e-050.00294767utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235439TGCTTGCCGCCCGGG[C/T]AGGGACAAGTGGCAC1877
rs565702323snpA/G0.001197370.0244387intron-variantE4F1GRCh38.p716:2233314CCACAGGGAGAGCAG[A/G]GCCAGTGGGAGCGCC1877
rs565876455snpC/G0.001197370.0244387intron-variantE4F1GRCh38.p716:2231994TCCACCTCTCACTCT[C/G]ACCTGGAGAGGTGAA1877
rs566143926snpC/G0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236130TGCTTTCCCTGAAGG[C/G]ATTCTGCTCAGGGAG1877
rs566292104snpG/T0.00239330.0345097intron-variantE4F1GRCh38.p716:2232040TGCTCGGACCTGTGT[G/T]TTGAGGGCTCAGTGC1877
rs566348970snpC/T0.0001013630.00711838intron-variantE4F1GRCh38.p716:2232730CCTGCTGGGGCTGCC[C/T]GGGGCTGACTAGGTT1877
rs566420745snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2223978GGCGCCTGTCATCCC[C/G]CCTCTCTGGTGTGCG1877
rs566426803snpA/C0.0008746040.0208935missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234919GCCCCGCGGCAGCCA[A/C]CACCGTCCTCACGGA1877
rs566643474snpA/G0.0007984030.0199641intron-variantE4F1GRCh38.p716:2229897CGGGGGCACACCCAG[A/G]CACCAGGGAGTCATT1877
rs566897811snpA/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222623CCTAGCACTTTGGGA[A/G]GCCGAAATGGGAAAA1877
rs566973067snpG/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228124AAGCGTGCTGTCAGG[G/T]CCACCCTCTGCTGGG1877
rs567182050snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2223100ATGAGCCATCCCCGA[C/T]CCGTGTTCTTTTCCC1877
rs567239912snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226096AGACTCCGCCTTGAA[A/G]GAAAAAAAAAAAAGA1877
rs567250531snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231270CCCTCCTGCCGCTTC[A/G]CGGAAAAAGTTCGCG1877
rs567487667snpC/T0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236007TGGGAGGACCAGGGA[C/T]GGGGACAGGGAGATC1877
rs567543806snpA/Cupstream-variant-2KBE4F1GRCh38.p716:2222181GAACCAAGATCGTGC[A/C]GTTGCATTCTAGCCT1877
rs567600771snpA/G0.005575420.0525036utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235688GAGGCGCCCCAAGAC[A/G]GACAGTGTACATAAG1877
rs567815872snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230777AAGACACTCATCAAT[A/G]CCACTCAGAGCTCGG1877
rs567882180snpG/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2234055GGCCGGGGTGCTTCT[G/T]GGTGTCCAGGGTGGG1877
rs567934857snpA/Gintron-variantE4F1GRCh38.p716:2226503CATAGCTGTGGTTTG[A/G]CCCTTTCTCCGCCCT1877
rs568055470snpG/Tintron-variantE4F1GRCh38.p716:2229368TGACCCTGGCCCGGG[G/T]GTGAAGGGATTGGAC1877
rs568128325snpA/C0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228587TGGGGGAGGTGGCCG[A/C]GCTTCAGGATGGACC1877
rs568471360snpC/Tintron-variantE4F1GRCh38.p716:2228626CGGTTCCGGGGGCCA[C/T]GTGGGCGGGCAGAGG1877
rs568521071snpC/T1.70043e-050.0029158missense, nc-transcript-variantE4F1GRCh38.p716:2232210TCGTGGCTGCTGAGG[C/T]GGAGCTGGGAGACGG1877
rs568522901snpC/Gintron-variantE4F1GRCh38.p716:2223992CCCCTCTCTGGTGTG[C/G]GTCCACAAGTGCTCG1877
rs568584625snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2223293CGCCAGTCCGCTCGC[C/T]CCTCGCGTTCTCTGG1877
rs568666125snpA/G0.002791620.0372561intron-variantE4F1GRCh38.p716:2227441CAGTGGTGTGATCTC[A/G]GCTCACTGCAAGCTC1877
rs568841564snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229970CGTGTCCCTCCCAGA[A/G]TCTTCCCCACTTCCC1877
rs569050435snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225409GAGGCTGAGGTGAGA[C/G]GATCACTTGAGCCCA1877
rs569328828snpA/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2223279GGCTGCCTAGCAGCC[A/G]CCAGTCCGCTCGCCC1877
rs569337480snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229017CGGGCGCTTGTCATC[C/T]GCATTGCACGGTCAG1877
rs569672809snpC/T0.0007984030.0199641downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235772GGCAGTGGCAGCCTC[C/T]GCGGCTGGTGCCACC1877
rs569841751snpA/G/T0.0001339570.00818304intron-variantE4F1GRCh38.p716:2229697CGACTTCCATGAATC[A/G/T]CTGGCCTGATAGACC1877
rs569878678snpC/Tintron-variantE4F1GRCh38.p716:2231810CAGGAGCAGTGGCAG[C/T]GAGCAGGACAGGCGG1877
rs569998442snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231391GTGTAAGGGCTCGGG[C/G]AGGAGAGGCTCTTAA1877
rs570063150snpA/G0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2236055ACCGCAGGGTGAGCA[A/G]GTGGAGCAGCAGCAG1877
rs570075736snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2233731TCGCCTCCCTGAAGT[A/G]GCTTTCTGCAGTGAC1877
rs570201178snpA/C0.0007984030.0199641intron-variantE4F1GRCh38.p716:2226166TGGGTTGAGGGTGGT[A/C]TTGTCTTTGTCCCCA1877
rs570282079snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229474CACCACAAGTCACAC[C/T]TCCACAGCTTTACAC1877
rs570400416snpA/C0.0007984030.0199641intron-variantE4F1GRCh38.p716:2229123CACCCCACTCTGAGC[A/C]TGTGCTCTTTACCTG1877
rs570462130snpC/T0.0001608910.00896771intron-variantE4F1GRCh38.p716:2234130GCGGCCTGGCGGGCC[C/T]GCGGGTGATGGGCTT1877
rs570527683snpG/T00upstream-variant-2KBE4F1GRCh38.p716:2223348AACATAGGTCCTTCT[G/T]CCGCCCCGCCCCCTG1877
rs570599480snpA/Gintron-variantE4F1GRCh38.p716:2229398CTGGGACCGGTGGTC[A/G]TGTTGGGGAAGAGGA1877
rs570828769snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2228050CTCTCTGGGCCTCTC[A/G]CCTGTCAGTCGCTGA1877
rs570937518snpC/T0.001146940.0239198intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223786GTAACCGGGCCGACC[C/T]GGAGGGTGCGGCCGG1877
rs570940715snpC/T0.007162660.059414intron-variantE4F1GRCh38.p716:2227496CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA1877
rs570940739snpA/C/G0.0001645830.00907016intron-variantE4F1GRCh38.p716:2233205GCGACGGGGGGCCCC[A/C/G]GAGGGCTGCTCTGTC1877
rs571067152snpA/C0.001197370.0244387upstream-variant-2KBE4F1GRCh38.p716:2221737CTGAGGCAGGCAGAT[A/C]GCTTGAACTCAGGAG1877
rs571193329snpC/T0.0004030590.0141904missense, synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2223630TGGAGGGCGCGATGG[C/T]AGTGCGGGTGACGGC1877
rs571303896snpC/T0.0007984030.0199641utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235677GGCACAGGATGGAGG[C/T]GCCCCAAGACGGACA1877
rs571352060snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2230644GAGGGGGTGGAGGAG[C/T]CGTGGCGGAGGCCAA1877
rs571352122snpC/T0.001596170.0282053intron-variantE4F1GRCh38.p716:2224848TGGATTGGATCTCAG[C/T]ACTGTGAAGGCCTTC1877
rs571576707snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226048CAGTGAGCTGAGATC[A/G]CCCCACTGCACTCCA1877
rs571722138snpC/T0.0003992810.0141238intron-variant, synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2223820GCGGGCAGTTCATCC[C/T]GGGCTGGCAGAGGCC1877
rs572185598snpG/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230996CCCTGTGCTTCAGCA[G/T]CCCCTCTTGGCACCC1877
rs572289248snpC/G2.08601e-050.00322949intron-variantE4F1GRCh38.p716:2232420CCCCTCCTGTTCCCC[C/G]AGGAGGGCCCTGAGC1877
rs572317980snpA/Gintron-variantE4F1GRCh38.p716:2227692TTTTAGTAGAGATGG[A/G]ATTTCACCATATTGG1877
rs572346538snpA/C0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226996GAGATGGCCACTCAC[A/C]TGCTCCAGGGCACGC1877
rs572408189snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2226267TGGCGAGGAGTCCCT[C/T]TAGAGGTTGCTGGGC1877
rs572487058snpA/G0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235794GGTGCCACCACCTTT[A/G]CCCAGGCCCCCGCAG1877
rs572559260in-del-/TC0.001197370.0244387intron-variantE4F1GRCh38.p716:2226194CCATAGGATTCATAG[-/TC]TCTGCCTTTTTTCCT1877
rs572599764snpA/G0.0007984030.0199641intron-variantE4F1GRCh38.p716:2226105CTTGAAAGAAAAAAA[A/G]AAAAGATGCAGATTG1877
rs572803733snpC/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2223474ACACCGCTATCCAGG[C/G]CCGGCTCCCCGCCTG1877
rs572931274snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2233824CCATGGTTGTGTTCT[C/T]GGTACTGCCAGGGCA1877
rs573362015snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2221827GCTAGTGATGGGCAC[C/T]TGTAGTCCCAGCTAC1877
rs573733612snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2231055CCCTTTGCGGGCATC[C/T]TGGGTACTCTGTGTG1877
rs573896911snpC/T0.0003992810.0141238downstream-variant-500B, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235848CCTAGACTCACGTGC[C/T]TGGCCGCCCCACCCA1877
rs574231509snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2230225TTTTATGAGCGTGCA[A/G]TGCCAGGACTCTTTG1877
rs574295861snpA/C/T0.0001897240.00973797utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235365CACCATCGCCACCCC[A/C/T]GAGAGCCTGACAGAG1877
rs574318798snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229768ATGCTCGTCTCTCCC[A/G]AGACCAGGGCCTGGC1877
rs574509932snpC/Gintron-variantE4F1GRCh38.p716:2224274GCCTGTGGCCCCTTC[C/G]AGTCCCACACTTGCC1877
rs574542864snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2221960CTCGGTGGCTCATGC[C/T]TGTCATCCCAGCACT1877
rs574745094snpA/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226872CTTGGGAACCAGTAA[A/T]GTCCCAAGTCAGTGA1877
rs574817067snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226409AAGGGGAAGAGGGTG[C/G]TGGGCACCTTAGAGC1877
rs574866341snpC/Gupstream-variant-2KBE4F1GRCh38.p716:2221724GTATGTAAGAGGGCT[C/G]AGGCAGGCAGATCGC1877
rs575101270snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2224197CTCCAGGATCTGGGC[C/T]CTGGGCCTGTCCGTA1877
rs575343524snpC/T0.0007984030.0199641intron-variantE4F1GRCh38.p716:2229225CTCTGCCGGATGTGG[C/T]GGGCTGGGACTGTGC1877
rs576046901snpA/G6.888e-050.00586816utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235395GCAGGTGGCCATGAC[A/G]CTGGCCTCGGCCATC1877
rs576148083snpC/T0.001994810.0315187intron-variantE4F1GRCh38.p716:2226538TTCAACAGTAAACAT[C/T]TGCCCAGCTCCTTCG1877
rs576266110snpA/G0.0001015540.00712507missense, nc-transcript-variantE4F1GRCh38.p716:2232275CAGGGGCTGGGGCTC[A/G]CAGGGGAGGGTGAGC1877
rs576345658snpC/T0.002597590.0359451synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232506CAGCCGCAAGGACCA[C/T]GAGTGCAAGCTCTGT1877
rs576388989snpA/C/T0.0004036990.014202intron-variant, synonymous-codon, missenseE4F1GRCh38.p716:2228311GGAGGAAAAGCCAGA[A/C/T]GGAGCCCTGGCTGCC1877
rs576405584snpC/Gutr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantE4F1GRCh38.p716:2223529CCCGCCCTCCTCTTG[C/G]CGTTCCCTCACGCTG1877
rs576440819snpC/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2227519TGGGACTATAGGCAC[C/G]TGCCACCATGCCTGG1877
rs576565106snpA/G1.66863e-050.0028884synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233048CTTGGGGACAGCCAC[A/G]TCATCGGTGACAGGC1877
rs576645711snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2225711TCCCGACCTCAGGTG[A/G]TCTGCCCGCCTCAGC1877
rs576926034snpC/G0.003189780.0398085intron-variantE4F1GRCh38.p716:2224527GGGTGCGGTGGCTCA[C/G]GCCTGTAATCCCAGC1877
rs577051440snpA/G0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222765CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT1877
rs577113610snpC/Gintron-variantE4F1GRCh38.p716:2226960TCAGTCTCCTGGGCC[C/G]CAGCCCATTTTACAG1877
rs577113994snpC/T0.0003992810.0141238upstream-variant-2KBE4F1GRCh38.p716:2222078TATAAAAAAATTAGC[C/T]GGGTGTGGTGGCAGT1877
rs577126270snpA/G7.07614e-050.00594775intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235168AGGGCAGGCGGGGGC[A/G]GGGAGGCTCCCTGGC1877
rs577462697snpA/G0.0003992810.0141238intron-variantE4F1GRCh38.p716:2226941CAGCCAGAGCCAGTG[A/G]GCATCAGTCTCCTGG1877
rs577647755in-del-/Aintron-variantE4F1GRCh38.p716:2226097ACTCCGCCTTGAAAG[-/A]AAAAAAAAAAAAGAT1877
rs577741405snpC/Tintron-variantE4F1GRCh38.p716:2230662TGGCGGAGGCCAACC[C/T]GGGGCCTGGGAAGGG1877
rs578188535snpC/T0.0003992810.0141238intron-variantE4F1GRCh38.p716:2229741CCAGAGGATGGGGCC[C/T]CTGCTGCCTGTATGC1877
rs745315027snpC/T3.46188e-050.00416032missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235124AGGCCACGGAGATCA[C/T]CGAGGGCACCCAGAC1877
rs745359999snpA/C/G6.50031e-050.00570071utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235585TAGCATGAGGTCTGC[A/C/G]GGGTCCTGGCCGGGC1877
rs745375897snpA/Gmissense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234933ACCACCGTCCTCACG[A/G]AAGACCCGCACACAG1877
rs745517753snpC/T1.69666e-050.00291256synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233157ATGCAGGAGCTGTCC[C/T]TGGGCATGAAAGCCC1877
rs745605757snpC/T1.77373e-050.00297797intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234423ACCCTGGCGCCTGAT[C/T]CCCCCATCCTGCTCC1877
rs745605953snpC/G0.001417030.0265802synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233063ATCATCGGTGACAGG[C/G]GAGCCTATAGAGACT1877
rs745661683snpA/Gintron-variantE4F1GRCh38.p716:2224799AAAGAAAAGAAAATG[A/G]CCAGGGTCACCCAGG1877
rs745711025snpC/T1.72665e-050.00293819utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235424TCAGCGAGGGCACTG[C/T]GCTTGCCGCCCGGGC1877
rs745770809snpC/Tintron-variantE4F1GRCh38.p716:2225588AAGCTATTCTCCTGA[C/T]TCGGCCTCCTGAGTA1877
rs745771766snpA/G/T6.91448e-050.00587948utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235357GACACCATCACCATC[A/G/T]CCACCCCCGAGAGCC1877
rs745803461snpC/T1.69178e-050.00290837synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228388TGAGGACGATGTGCA[C/T]AGATGCGGCCGCTGC1877
rs745913566snpA/Gupstream-variant-2KBE4F1GRCh38.p716:2223073GAATAAAACAGCTTC[A/G]CAGAGCTACCCATGA1877
rs746000717snpA/G0.0002539040.0112644missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233597AGTCCCCAGCCCCTG[A/G]CAGTGGCAGCCCCGC1877
rs746018946snpC/G2.12538e-050.00325982missense, nc-transcript-variantE4F1GRCh38.p716:2223635GGCGCGATGGCAGTG[C/G]GGGTGACGGCCGCTC1877
rs746078819snpC/T1.68829e-050.00290537synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234929AGCCACCACCGTCCT[C/T]ACGGAAGACCCGCAC1877
rs746084073snpA/T2.49753e-050.0035337utr-variant-5-prime, missense, nc-transcript-variantE4F1GRCh38.p716:2223581ATGACGACATGGTCG[A/T]AAATCCGCCATCTTC1877
rs746117638in-del-/C5.31684e-050.00515571intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234422ACCCTGGCGCCTGAT[-/C]CCCCCCATCCTGCTC1877
rs746170340snpA/G1.65913e-050.00288017missense, nc-transcript-variantE4F1GRCh38.p716:2229642GAGGCGGCCTCTCTG[A/G]CAGCAGACATCAGCC1877
rs746234698snpA/Gintron-variantE4F1GRCh38.p716:2228586GTGGGGGAGGTGGCC[A/G]CGCTTCAGGATGGAC1877
rs746372944snpA/G3.32458e-050.00407698missense, nc-transcript-variantE4F1GRCh38.p716:2232890GACGTGGTTGTCAGC[A/G]AAGAGGACGCACGTG1877
rs746462506snpA/G1.86562e-050.00305414intron-variantE4F1GRCh38.p716:2234152GATGGGCTTGGCCTG[A/G]TGCTGTGTGTGGCTG1877
rs746486192snpA/G6.13591e-050.00553857intron-variant, splice-acceptor-variantE4F1GRCh38.p716:2228290GGGGGAATCTGTTCT[A/G]GGGCTGGAGGAAAAG1877
rs746533922snpA/G1.76428e-050.00297003stop-gained, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235218CGTGGCCCTGCAGGT[A/G]GACAGCCACATCATG1877
rs746571873snpC/G0.0001624560.0090112intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223828TTCATCCCGGGCTGG[C/G]AGAGGCCCGGATGGC1877
rs746572305snpA/G2.01379e-050.0031731intron-variantE4F1GRCh38.p716:2232382GAGCCGGCGTGCGGG[A/G]AGCCAGTGTGTGGGT1877
rs746609306in-del-/Gutr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantE4F1GRCh38.p716:2223544CCGTTCCCTCACGCT[-/G]GCCTCGGCGCGGCCC1877
rs746655240snpA/G3.4915e-050.00417807intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235149CCAGACAGAGGTGAG[A/G]GGTAGGGCAGGCGGG1877
rs746661970snpA/G0.0001048250.0072389missense, nc-transcript-variantE4F1GRCh38.p716:2232320CTACTGGTGAACAAG[A/G]ATGGCCGCTATGTGT1877
rs746759448snpA/G4.60585e-050.00479866intron-variantE4F1GRCh38.p716:2233395GGGTGGGTGCTGGAT[A/G]CCAGGCTGCCTGGCC1877
rs746821546snpA/Gupstream-variant-2KBE4F1GRCh38.p716:2222284GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCGT1877
rs746851555snpA/G3.92241e-050.00442838synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234633GGAGAAGCCGCACGT[A/G]TGCCAGTTCTGCAGC1877
rs746895780snpA/G6.7086e-050.00579124intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234540GGAGAGCTGTAGTCT[A/G]TTGTGGCCAAGGCCA1877
rs746918557snpA/G1.91562e-050.00309479utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235497ATCAGAGGACATCGA[A/G]ATCCTGGAGCATGCA1877
rs746928089snpC/T1.81082e-050.00300895intron-variantE4F1GRCh38.p716:2228533CAGGAGGTGAGCCCT[C/T]ACCCACTCCCCCATC1877
rs747006590snpA/G1.73342e-050.00294394utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235432GGCACTGTGCTTGCC[A/G]CCCGGGCAGGGACAA1877
rs747033101snpC/Gintron-variantE4F1GRCh38.p716:2229502CACTGGCAGAGCCCA[C/G]GCCTCTTCTCTGAGA1877
rs747064418snpC/T1.69611e-050.00291209missense, nc-transcript-variantE4F1GRCh38.p716:2228471CCTGCCAGCGGGCCC[C/T]TCCGGAGGCCCTGCC1877
rs747116239in-del-/A0.0003172090.0125898intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234803GCCGGTGGAGGTGGG[-/A]GGGGGAGGGGAGGGG1877
rs747217683snpC/G4.99463e-050.00499707missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233894CAGCAGGTGGCCAGC[C/G]AGGCCTCAGCGGTGC1877
rs747307359snpA/G0.0002950290.012142synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233620AGCCCCGCAGCTGCC[A/G]GTACTGGAAGTGCAG1877
rs747387668snpA/Gintron-variantE4F1GRCh38.p716:2227396GTTTTTTTTGAAACG[A/G]AGTCTCGCTCTTTCG1877
rs747510999snpA/C/T3.69101e-050.0042958intron-variantE4F1GRCh38.p716:2228541GAGCCCTCACCCACT[A/C/T]CCCCATCCCCTCCCG1877
rs747601217snpC/T1.68414e-050.0029018intron-variantE4F1GRCh38.p716:2232952CCTGGGGGCTGGCTG[C/T]GGACGCAGCCGCCAC1877
rs747632415snpC/T1.67416e-050.00289318missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234303AGCTCTACAAGACCA[C/T]TGCCCATGTGCGTGG1877
rs747666310snpC/T3.53064e-050.00420142intron-variant, synonymous-codonE4F1GRCh38.p716:2228358AGGCCCTGCTGACAG[C/T]AGGCTCGTTGCAGAT1877
rs747733148snpC/T5.22198e-050.00510952utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235293GATCATCGTGCAGAA[C/T]GTCACCATGGACGAG1877
rs747767152snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2221882AGTGAGCTGAGATCA[C/T]GGCACTGCACTCCAG1877
rs747806181snpA/G7.66019e-050.0061883intron-variant, missenseE4F1GRCh38.p716:2228309CTGGAGGAAAAGCCA[A/G]ACGGAGCCCTGGCTG1877
rs747908249in-del-/C7.64906e-050.00618381intron-variantE4F1GRCh38.p716:2233876GACCTTCCTGTGGTT[-/C]CCCAGCAGGTGGCCA1877
rs747928080snpG/Tintron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234453CCTGGCCGTGGCCCA[G/T]GTGCACCCCCTTCCC1877
rs747930778snpC/G2.06776e-050.00321533intron-variantE4F1GRCh38.p716:2232400CCAGTGTGTGGGTGG[C/G]AGGCCCCCTCCTGTT1877
rs747936086snpC/T5.43149e-050.005211missense, nc-transcript-variantE4F1GRCh38.p716:2232339GCCGCTATGTGTGTG[C/T]GCTGTGCCACAAGAC1877
rs747998671in-del-/C1.96273e-050.00313261intron-variant, frameshift-variantE4F1GRCh38.p716:2228339CCCAGCCTCCGCCTT[-/C]CCCAGGCCCTGCTGA1877
rs748010768snpA/C2.47767e-050.00351962missense, nc-transcript-variantE4F1GRCh38.p716:2233495CGTGAGAACCTGCTG[A/C]ACCAGGCCATGCAGA1877
rs748019819snpC/T3.72849e-050.00431753intron-variantE4F1GRCh38.p716:2233430TCCTCTCTCTGCCTC[C/T]CCTGCAGCCCCCCGT1877
rs748161592snpA/Gupstream-variant-2KBE4F1GRCh38.p716:2222182AACCAAGATCGTGCC[A/G]TTGCATTCTAGCCTA1877
rs748169224snpC/T4.53155e-050.0047598stop-gained, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234658TGCAGCCGTGGCTTC[C/T]GAGAGAAGGGCTCAC1877
rs748182529snpA/C1.66638e-050.00288645intron-variantE4F1GRCh38.p716:2229554CGACTCCCCTGTTTT[A/C]TTCCCCCTTTGGCAG1877
rs748247093snpC/Tintron-variantE4F1GRCh38.p716:2229978TCCCAGAATCTTCCC[C/T]ACTTCCCTGCCACCC1877
rs748279043snpC/T9.96264e-050.00705714synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232865GAAAATCCGCTTCAG[C/T]GTGAGCAAGGACGTG1877
rs748293568snpC/Tintron-variantE4F1GRCh38.p716:2230049AGGCACCCACCAGAA[C/T]GGCCCACTCGCCCAG1877
rs748369000snpG/T3.35807e-050.00409747missense, nc-transcript-variantE4F1GRCh38.p716:2232757GGTTCTCTCTGCAGA[G/T]GAGCGCCCCTACAAG1877
rs748400100snpC/T4.71109e-050.00485317synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233983GGCCCACAAGAGGGG[C/T]CACACCGGTAGGTGA1877
rs748490046snpA/G8.64207e-050.00657289missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235098CACTGCGGACGATGC[A/G]GAGACCAGTGAGGCC1877
rs748540599snpC/T8.97143e-050.00669695missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233904CCAGCGAGGCCTCAG[C/T]GGTGCCCAGGACCCA1877
rs748576332snpC/G/T3.52206e-050.00419631synonymous-codon, missense, nc-transcript-variantE4F1GRCh38.p716:2223727GGCGGCGGCCTTGGC[C/G/T]CCCAGCGGCTTCCTC1877
rs748664813snpC/T4.07805e-050.00451537intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235017GTGGGTGTGGGGCCC[C/T]GGGGCCGTGCTGGGA1877
rs748690987snpC/G/T3.3694e-050.0041044missense, nc-transcript-variantE4F1GRCh38.p716:2232242GAGATGGCCGAGGCC[C/G/T]CGGGCAGCCCCCGCC1877
rs748694000snpA/C1.71114e-050.00292496missense, nc-transcript-variantE4F1GRCh38.p716:2232185GGTGGTGGGCACATC[A/C]AAGAGGTCATCGTGG1877
rs748790884snpA/Gintron-variantE4F1GRCh38.p716:2224884CCCTTTAACTTCCGG[A/G]CTCTGCTGCCTCATA1877
rs748906678snpC/G1.68357e-050.00290131missense, nc-transcript-variantE4F1GRCh38.p716:2228455CACAAGATTCAGAAG[C/G]CCTGCCAGCGGGCCC1877
rs748928929snpA/G1.67399e-050.00289304synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234313GACCATTGCCCATGT[A/G]CGTGGCCACCGGCGC1877
rs748984863snpC/Tintron-variantE4F1GRCh38.p716:2226830TGCACGACCGGGGTC[C/T]GGCACAGCAATGGTG1877
rs749016844snpC/G7.0028e-050.00591685utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235344GGCGGCTGCCGCCGA[C/G]ACCATCACCATCGCC1877
rs749054992snpA/Tintron-variantE4F1GRCh38.p716:2225326TGGGTCTGTACCCTC[A/T]GAGCTTGTCCTATGA1877
rs749101506snpA/G1.7402e-050.0029497utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235308CGTCACCATGGACGA[A/G]GAGACGGCGCTGGGC1877
rs749141504snpA/G5.73839e-050.00535618missense, nc-transcript-variantE4F1GRCh38.p716:2232496TCACTCACAGCAGCC[A/G]CAAGGACCACGAGTG1877
rs749206599snpG/Tmissense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233509GCACCAGGCCATGCA[G/T]AACTCCGGCATCGTC1877
rs749230680snpA/G6.25202e-050.00559072intron-variantE4F1GRCh38.p716:2232413GGCAGGCCCCCTCCT[A/G]TTCCCCCAGGAGGGC1877
rs749236840snpA/G1.74839e-050.00295663missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233582CCTGCTGCCGGGTCC[A/G]GTCCCCAGCCCCTGG1877
rs749272911snpC/T0.0001059940.00727913synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234923CGCGGCAGCCACCAC[C/T]GTCCTCACGGAAGAC1877
rs749334486snpA/G2.56157e-050.00357872utr-variant-5-prime, nc-transcript-variantE4F1GRCh38.p716:2223568GCGGCCCGTTGTTAT[A/G]ACGACATGGTCGTAA1877
rs749451593snpA/G5.67135e-050.0053248missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234676GAGAAGGGCTCACTG[A/G]TGCGGCACGTGCGAC1877
rs749481310snpC/Tmissense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234344GTCCACTCAGACGAG[C/T]GGCCCTACCCTTGTC1877
rs749515737snpA/G4.98434e-050.00499192synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2229578TTGGCAGGTGGTGCC[A/G]GCAGCACCAGGCCCA1877
rs749655806snpG/T1.94865e-050.00312136intron-variantE4F1GRCh38.p716:2234137GGCGGGCCCGCGGGT[G/T]ATGGGCTTGGCCTGA1877
rs749680829snpC/Tintron-variantE4F1GRCh38.p716:2231117TTAGTCCAGGGCTGC[C/T]AGCTCTCCTGTTGGC1877
rs749705386snpC/T1.67416e-050.00289318synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232769AGATGAGCGCCCCTA[C/T]AAGTGCTCCAAGTGT1877
rs749793321snpA/G5.27858e-050.00513713missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233990AAGAGGGGCCACACC[A/G]GTAGGTGATGGGTGG1877
rs749804408snpA/G1.77068e-050.00297541intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235201AGCCGCTCTTGCTGA[A/G]CCGTGGCCCTGCAGG1877
rs749813849snpA/C0.0001351810.00822023intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223815GGGGTGCGGGCAGTT[A/C]ATCCCGGGCTGGCAG1877
rs749988881snpA/G7.47747e-050.00611406synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234711CACAGGCGAGAAGCC[A/G]TTCAAGTGCTACAAG1877
rs750073803snpA/G/T0.00019780.00994311synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234627CCTGGAGGAGAAGCC[A/G/T]CACGTGTGCCAGTTC1877
rs750115247snpA/G1.67066e-050.00289016intron-variantE4F1GRCh38.p716:2229537ACTCTGGAGCATACA[A/G]ACGACTCCCCTGTTT1877
rs750129537in-del-/G00intron-variantE4F1GRCh38.p716:2233194AGAGGTGGGGGCGAC[-/G]GGGGGGCCCCGGAGG1877
rs750143067snpC/T1.66065e-050.00288149missense, nc-transcript-variantE4F1GRCh38.p716:2232816AGTCGGGTGCACTGA[C/T]CCGGCACCTCAAGTC1877
rs750226059snpC/Tintron-variantE4F1GRCh38.p716:2226579CTGGGTTTGATCCTG[C/T]CGAGGGACTGAAGGT1877
rs750233058snpC/T2.08335e-050.00322744intron-variantE4F1GRCh38.p716:2234124TGGCAGGCGGCCTGG[C/T]GGGCCCGCGGGTGAT1877
rs750279613snpC/T1.69115e-050.00290782intron-variantE4F1GRCh38.p716:2232719CTTGTCGCCAGCCTG[C/T]TGGGGCTGCCCGGGG1877
rs750373926snpA/Gintron-variantE4F1GRCh38.p716:2228160ACCTCCTGAGGGTGG[A/G]TCTGGCCCCTGCAGA1877
rs750399846snpG/T9.85367e-050.00701845intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223790CCGGGCCGACCCGGA[G/T]GGTGCGGCCGGGGTG1877
rs750461810snpC/Tupstream-variant-2KBE4F1GRCh38.p716:2222009CGGATCACCTGAGGT[C/T]AGGAGTTCAAAACCA1877
rs750479852snpA/Gmissense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234284CGCTGTGGCGACTGC[A/G]GGAAGCTCTACAAGA1877
rs750488930snpG/T3.37901e-050.00411022missense, nc-transcript-variantE4F1GRCh38.p716:2232270GCCAGCAGGGGCTGG[G/T]GCTCGCAGGGGAGGG1877
rs750543799snpA/G5.67006e-050.0053242intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234989AGCTGACACCCAGGA[A/G]TATATCATCGAGGTG1877
rs750664055snpC/T5.04927e-050.00502432intron-variantE4F1GRCh38.p716:2229707GAATCGCTGGCCTGA[C/T]AGACCTTCGTGGTTG1877
rs750675436snpA/G1.6633e-050.00288378missense, nc-transcript-variantE4F1GRCh38.p716:2233106CACCTGGTGACAGAT[A/G]CCAAGGGCACCGTCA1877
rs750763458snpC/T3.35345e-050.00409465synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234352AGACGAGCGGCCCTA[C/T]CCTTGTCCCAAGTGT1877
rs750767205snpC/T0.000167090.00913877synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233030TGGAGCTGGAGCTGC[C/T]GGCTTGGGGACAGCC1877
rs750857483snpC/T1.67478e-050.00289372synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234292CGACTGCGGGAAGCT[C/T]TACAAGACCATTGCC1877
rs750922254snpA/Gintron-variantE4F1GRCh38.p716:2224404CCCTTATCCTGCTTT[A/G]GGTTTTTTCATTCTC1877
rs750945693snpA/T1.7782e-050.00298173missense, nc-transcript-variantE4F1GRCh38.p716:2232552ACCAAGGGCTCACTC[A/T]TCCGGCACCACCGGC1877
rs750945798snpC/T0.0001292810.0080389intron-variant, missenseE4F1GRCh38.p716:2228347TCCGCCTTCCCAGGC[C/T]CTGCTGACAGCAGGC1877
rs750966173snpG/Tintron-variantE4F1GRCh38.p716:2230772CGACCAAGACACTCA[G/T]CAATGCCACTCAGAG1877
rs751032252snpC/T2.01871e-050.00317697intron-variantE4F1GRCh38.p716:2232450CTGCCACGCCCTCCC[C/T]CACAGGGCAGCATCC1877
rs751100321in-del-/CCT4.30877e-050.00464133intron-variantE4F1GRCh38.p716:2233413AGGCTGCCTGGCCAG[-/CCT]CCTCTCTCTGCCTCC1877
rs751126806snpA/G5.56375e-050.00527405missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233543GAGCGCGCTGCTGGG[A/G]AGGAGGGTGCCCTGG1877
rs751216480snpA/T0.0007144390.0188867intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234846CTAGCCCTGACCGAG[A/T]CCCCACCCACAGGGG1877
rs751255718snpA/G1.76294e-050.0029689missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234734GCTACAAGTGCGGCC[A/G]TGGCTTCGCCGAGCA1877
rs751372530snpA/C/G4.99117e-050.00499537missense, nc-transcript-variantE4F1GRCh38.p716:2232903GCAAAGAGGACGCAC[A/C/G]TGCAGGTCAGCATGG1877
rs751433198snpC/T1.66779e-050.00288768intron-variantE4F1GRCh38.p716:2229547ATACAGACGACTCCC[C/T]TGTTTTCTTCCCCCT1877
rs751508046snpA/Gintron-variantE4F1GRCh38.p716:2231742CAGCCCATCTCCTCC[A/G]ATGGAAGAGTGGCCC1877
rs751547314snpA/Gintron-variantE4F1GRCh38.p716:2224566AGGTCGAGACGGGCG[A/G]GTCACGAGGTCAGGA1877
rs751586767snpA/G2.02325e-050.00318054intron-variantE4F1GRCh38.p716:2234127CAGGCGGCCTGGCGG[A/G]CCCGCGGGTGATGGG1877
rs751663604snpC/G0.000186550.00965609intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223893AGACACCTCGCGGAT[C/G]TCGCGGGACCCTCAC1877
rs751674551snpA/G4.21861e-050.00459252synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233965GACAGCAGCCACCCT[A/G]GAGGCCCACAAGAGG1877
rs751676637snpC/G1.77297e-050.00297734intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235174GGCGGGGGCGGGGAG[C/G]CTCCCTGGCACAGCC1877
rs751753632snpC/T3.97551e-050.00445825intron-variant, synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2223799CCCGGAGGGTGCGGC[C/T]GGGGTGCGGGCAGTT1877
rs751916028snpC/G0.0001997040.0099906intron-variantE4F1GRCh38.p716:2233202GGGGCGACGGGGGGC[C/G]CCGGAGGGCTGCTCT1877
rs751937000snpA/G5.05685e-050.00502809missense, nc-transcript-variantE4F1GRCh38.p716:2232236GACGGTGAGATGGCC[A/G]AGGCCCCGGGCAGCC1877
rs751992468snpA/Gupstream-variant-2KBE4F1GRCh38.p716:2221823ATTAGCTAGTGATGG[A/G]CACCTGTAGTCCCAG1877
rs752006264snpA/G0.000103290.0071857synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234588GTCTCCACAGAACGC[A/G]CAGCAGGTGCACTTC1877
rs752025643snpA/G3.44756e-050.0041517missense, nc-transcript-variantE4F1GRCh38.p716:2228503GCCACCCCTGCCACC[A/G]CAGCGTTGCTGGGCC1877
rs752143172snpG/T1.72178e-050.00293404utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235402GCCATGACGCTGGCC[G/T]CGGCCATCAGCGAGG1877
rs752283262snpC/T3.51568e-050.00419251utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235338CCCAGAGGCGGCTGC[C/T]GCCGACACCATCACC1877
rs752306108snpC/T0.0001417110.00841637missense, nc-transcript-variantE4F1GRCh38.p716:2232567ATCCGGCACCACCGG[C/T]GGCACACGGGTGAGC1877
rs752344146snpC/Tintron-variantE4F1GRCh38.p716:2229299CTCCCTCCCTGCAGG[C/T]GCCCTGTGCTCCAGG1877
rs752392892snpA/G0.001088310.0233017synonymous-codon, missense, nc-transcript-variantE4F1GRCh38.p716:2223685CGAAGCCGGGCGGGA[A/G]GCGGGCGAGGGTGCA1877
rs752492992snpC/T0.0004015440.0141637intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234968GGTGGAGTTCTCGTC[C/T]GTGGTAGCTGACACC1877
rs752495113snpG/T1.72472e-050.00293654missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233573GAGCCAGCTCCTGCT[G/T]CCGGGTCCAGTCCCC1877
rs752553910snpA/G1.66513e-050.00288537intron-variantE4F1GRCh38.p716:2229678TCTGACCTTGTTGGT[A/G]AGCCGACTTCCATGA1877
rs752582808snpA/C0.000117640.00766852synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234908GTCTGAGGACAGCCC[A/C]GCGGCAGCCACCACC1877
rs752641682snpC/T1.65858e-050.00287969synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2229620CACTGTGGCCCACAT[C/T]GTGGTGGAGGCGGCC1877
rs752646018snpA/C3.34588e-050.00409002intron-variantE4F1GRCh38.p716:2232985GGGTGTGTGAGGGAT[A/C]TTCACTCCCTCACTC1877
rs752735909snpA/G1.66521e-050.00288544intron-variantE4F1GRCh38.p716:2232913CGCACGTGCAGGTCA[A/G]CATGGTGCGGGCAGC1877
rs752795153snpC/Gintron-variantE4F1GRCh38.p716:2226473GACTCTGTTGGGTGG[C/G]CCCTGCAGGCGAGTC1877
rs752817543snpA/Cupstream-variant-2KBE4F1GRCh38.p716:2223313GCGTTCTCTGGCTCT[A/C]AAATCCGAGTGCAGC1877
rs752962126snpC/T0.0001599420.00894123intron-variantE4F1GRCh38.p716:2234132GGCCTGGCGGGCCCG[C/T]GGGTGATGGGCTTGG1877
rs752989811snpC/G0.0001980.00994791intron-variantE4F1GRCh38.p716:2223943AGGTTTGCTGCGACC[C/G]TCACGGGCCTCTCCT1877
rs753059691snpC/G0.0001196630.00773416missense, nc-transcript-variantE4F1GRCh38.p716:2232298GGGTGAGCAGGCCCA[C/G]GTGAAGCTACTGGTG1877
rs753134859snpA/G/T0.0001891630.00972358intron-variantE4F1GRCh38.p716:2233233GTCTTCTGCCTGCTC[A/G/T]GTGCCAGTCTTTGTT1877
rs753182356snpC/Tintron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235076CCTTCTGCCCATCTG[C/T]CCAGGCCACTGCGGA1877
rs753257858snpG/T2.18759e-050.00330718intron-variantE4F1GRCh38.p716:2228573GTTCACCTGACAGGT[G/T]GGGGAGGTGGCCGCG1877
rs753386458snpC/T1.79696e-050.00299741utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235475AGGCCACTGTGACCA[C/T]GGTGTCATCAGAGGA1877
rs753476220snpA/C1.72326e-050.0029353utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235410GCTGGCCTCGGCCAT[A/C]AGCGAGGGCACTGTG1877
rs753559375snpC/T1.69238e-050.00290888intron-variantE4F1GRCh38.p716:2232709GCCTTGTCACCTTGT[C/T]GCCAGCCTGCTGGGG1877
rs753622918snpA/Gintron-variantE4F1GRCh38.p716:2229105ATGATGCTGGACCCT[A/G]GACACCCCACTCTGA1877
rs753628444snpC/T1.74467e-050.00295348intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235068ACCTCTGTCCTTCTG[C/T]CCATCTGCCCAGGCC1877
rs753644907snpA/G1.76808e-050.00297323synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232575CCACCGGCGGCACAC[A/G]GGTGAGCTGGCCGCA1877
rs753648277snpC/G3.85334e-050.00438922missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233943CTCAGTGCAGTGAGA[C/G]CTTCCCGACAGCAGC1877
rs753711774snpC/T1.67668e-050.00289537synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228442GGATTTTGTTCAGCA[C/T]AAGATTCAGAAGGCC1877
rs753736178snpC/G1.68069e-050.00289882intron-variantE4F1GRCh38.p716:2233859CTGCCCCGGGTGCTG[C/G]AGACCTTCCTGTGGT1877
rs753813526snpA/G1.65641e-050.00287781intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234974GTTCTCGTCCGTGGT[A/G]GCTGACACCCAGGAG1877
rs753827991snpA/C/T8.48233e-050.00651194missense, nc-transcript-variantE4F1GRCh38.p716:2232216CTGCTGAGGCGGAGC[A/C/T]GGGAGACGGTGAGAT1877
rs753924202snpA/G0.000116820.00764173missense, nc-transcript-variantE4F1GRCh38.p716:2233019CTTGAAGGTTCTGGA[A/G]CTGGAGCTGCCGGCT1877
rs754184318snpC/T3.45316e-050.00415507missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2234192GGCCGTTCGCCTGCG[C/T]GCAGTGTGGCAAGGC1877
rs754200639snpC/T2.00102e-050.00316302intron-variant, synonymous-codonE4F1GRCh38.p716:2228337CTGCCCAGCCTCCGC[C/T]TTCCCAGGCCCTGCT1877
rs754240768in-del-/GGGTGT1.67534e-050.0028942intron-variantE4F1GRCh38.p716:2232969ACGCAGCCGCCACTG[-/GGGTGT]GGGTGTGTGAGGGAT1877
rs754298020snpC/G1.74668e-050.00295518utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235272CCAGGCTAGCGCCGG[C/G]CACCAGATCATCGTG1877
rs754421089snpC/T1.77979e-050.00298306intron-variant, synonymous-codonE4F1GRCh38.p716:2228355CCCAGGCCCTGCTGA[C/T]AGCAGGCTCGTTGCA1877
rs754551029snpC/G7.22831e-050.00601135missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233552GCTGGGGAGGAGGGT[C/G]CCCTGGAGCCAGCTC1877
rs754597262snpA/C2.021e-050.00317877intron-variantE4F1GRCh38.p716:2232387GGCGTGCGGGGAGCC[A/C]GTGTGTGGGTGGCAG1877
rs754623104snpC/G0.0001384370.00831862missense, nc-transcript-variantE4F1GRCh38.p716:2228486CTCCGGAGGCCCTGC[C/G]TGCCACCCCTGCCAC1877
rs754715232snpC/T2.46436e-050.00351016synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2233492AGCCGTGAGAACCTG[C/T]TGCACCAGGCCATGC1877
rs754733023snpC/T1.97799e-050.00314476synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234885CTGGAGGTGGAGGAG[C/T]TGCTGGTGTCTGAGG1877
rs754821128snpA/G0.0001062640.00728841missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234742TGCGGCCGTGGCTTC[A/G]CCGAGCACGGCACGC1877
rs754829654snpC/T1.65853e-050.00287964synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2229614GCCCATCACTGTGGC[C/T]CACATCGTGGTGGAG1877
rs754853164snpC/T1.66782e-050.0028877intron-variantE4F1GRCh38.p716:2229548TACAGACGACTCCCC[C/T]GTTTTCTTCCCCCTT1877
rs754933280in-del-/CA4.19948e-050.0045821intron-variantE4F1GRCh38.p716:2233416TGCCTGGCCAGCCTC[-/CA]CTCTCTCTGCCTCCC1877
rs755001971snpC/T2.00813e-050.00316864utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235507ATCGAGATCCTGGAG[C/T]ATGCAGGCGAGCTGG1877
rs755060372snpC/T1.68227e-050.00290018intron-variantE4F1GRCh38.p716:2232748GGCTGACTAGGTTCT[C/T]TCTGCAGATGAGCGC1877
rs755148355snpA/G8.61623e-050.00656306missense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233969GCAGCCACCCTGGAG[A/G]CCCACAAGAGGGGCC1877
rs755186314snpC/T3.55764e-050.00421746intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235180GGCGGGGAGGCTCCC[C/T]GGCACAGCCGCTCTT1877
rs755203704snpA/G5.18704e-050.0050924synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235093CAGGCCACTGCGGAC[A/G]ATGCGGAGACCAGTG1877
rs755324797snpC/G5.09775e-050.00504838missense, nc-transcript-variantE4F1GRCh38.p716:2232287CTCGCAGGGGAGGGT[C/G]AGCAGGCCCAGGTGA1877
rs755412650snpC/T1.68516e-050.00290268missense, nc-transcript-variantE4F1GRCh38.p716:2232240GTGAGATGGCCGAGG[C/T]CCCGGGCAGCCCCCG1877
rs755569656snpA/G5.20458e-050.005101intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234403GGTGGGTCTCTGGCC[A/G]CAGGACCCTGGCGCC1877
rs755582316snpC/T1.67388e-050.00289294synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234310CAAGACCATTGCCCA[C/T]GTGCGTGGCCACCGG1877
rs755607071snpA/G/T3.35916e-050.00409815missense, nc-transcript-variantE4F1GRCh38.p716:2228450TTCAGCACAAGATTC[A/G/T]GAAGGCCTGCCAGCG1877
rs755627850snpC/T1.72311e-050.00293518utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235403CCATGACGCTGGCCT[C/T]GGCCATCAGCGAGGG1877
rs755635964snpA/Gintron-variantE4F1GRCh38.p716:2227785GGATTACAGGTGTGA[A/G]CCACCACACCCAGCC1877
rs755691762in-del-/CTintron-variantE4F1GRCh38.p716:2231984GAGGTGTCTCTCCAC[-/CT]CTCACTCTGACCTGG1877
rs755698323snpA/G1.76702e-050.00297234missense, nc-transcript-variantE4F1GRCh38.p716:2232571GGCACCACCGGCGGC[A/G]CACGGGTGAGCTGGC1877
rs755713708snpA/G3.51457e-050.00419185utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235339CCAGAGGCGGCTGCC[A/G]CCGACACCATCACCA1877
rs755724364snpC/Tintron-variantE4F1GRCh38.p716:2224833TTAAGTAGCAAGGGT[C/T]GGATTGGATCTCAGC1877
rs755758908snpC/Tintron-variantE4F1GRCh38.p716:2225136GAGAATTGCTTGAGC[C/T]CAGGAGACGGAGGTC1877
rs755767387snpC/T0.0001220350.00781042intron-variant, synonymous-codonE4F1GRCh38.p716:2228364TGCTGACAGCAGGCT[C/T]GTTGCAGATGAGGAC1877
rs755899887snpA/G0.0005539860.0166339intron-variantE4F1GRCh38.p716:2233851GGCACAGCCTGCCCC[A/G]GGTGCTGGAGACCTT1877
rs755934998in-del-/G3.49871e-050.00418238intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2234413TGGCCGCAGGACCCT[-/G]GCGCCTGATCCCCCC1877
rs755989987snpC/T0.001618120.0283979synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2233575GCCAGCTCCTGCTGC[C/T]GGGTCCAGTCCCCAG1877
rs755991498snpG/T1.66214e-050.00288278utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantE4F1GRCh38.p716:2223563TCGGCGCGGCCCGTT[G/T]TTATGACGACATGGT1877
rs756118944snpA/G3.31724e-050.00407248missense, nc-transcript-variantE4F1GRCh38.p716:2229621ACTGTGGCCCACATC[A/G]TGGTGGAGGCGGCCT1877
rs756120643snpA/Tupstream-variant-2KBE4F1GRCh38.p716:2223070AAAGAATAAAACAGC[A/T]TCGCAGAGCTACCCA1877
rs756166762snpC/T3.9116e-050.00442227missense, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234755TCGCCGAGCACGGCA[C/T]GCTGAACCGGCACCT1877
rs756206720snpA/C1.66571e-050.00288587intron-variantE4F1GRCh38.p716:2229557CTCCCCTGTTTTCTT[A/C]CCCCTTTGGCAGGTG1877
rs756210915snpA/G1.66527e-050.00288549intron-variantE4F1GRCh38.p716:2232915CACGTGCAGGTCAGC[A/G]TGGTGCGGGCAGCTG1877
rs756240490snpA/Cmissense, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2234238CCTGCTCAAGAAGCA[A/C]CAGGAGGTGCACGTG1877
rs756247708snpA/C/T1.74598e-050.00295459utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235323GGAGACGGCGCTGGG[A/C/T]CCAGAGGCGGCTGCC1877
rs756271380snpA/Gupstream-variant-2KBE4F1GRCh38.p716:2222101GTGGCAGTTGCCTGT[A/G]GTCCCAGCTACTCAG1877
rs756300887snpA/G6.64452e-050.00576352missense, nc-transcript-variantE4F1GRCh38.p716:2232876TCAGTGTGAGCAAGG[A/G]CGTGGTTGTCAGCAA1877
rs756332641snpC/T5.19197e-050.00509482synonymous-codon, intron-variant, nc-transcript-variantE4F1GRCh38.p716:2234190GAGGCCGTTCGCCTG[C/T]GCGCAGTGTGGCAAG1877
rs756353590snpA/C/G3.97371e-050.00445727intron-variantE4F1GRCh38.p716:2234133GCCTGGCGGGCCCGC[A/C/G]GGTGATGGGCTTGGC1877
rs756374186snpC/T0.0001593370.0089243intron-variantE4F1GRCh38.p716:2223977GGGCGCCTGTCATCC[C/T]CCCTCTCTGGTGTGC1877
rs756439711snpC/T7.09358e-050.00595507intron-variant, upstream-variant-2KBE4F1, DNASE1L2GRCh38.p716:2235189GCTCCCTGGCACAGC[C/T]GCTCTTGCTGAGCCG1877
rs756577645snpA/C2.0649e-050.00321311intron-variant, missense, nc-transcript-variantE4F1GRCh38.p716:2223810CGGCCGGGGTGCGGG[A/C]AGTTCATCCCGGGCT1877
rs756596489snpA/G6.91898e-050.00588134missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235116GACCAGTGAGGCCAC[A/G]GAGATCATCGAGGGC1877
rs756620926snpA/G1.71502e-050.00292827synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2232304GCAGGCCCAGGTGAA[A/G]CTACTGGTGAACAAG1877
rs756713317snpC/T5.67628e-050.00532712intron-variantE4F1GRCh38.p716:2233232TGTCTTCTGCCTGCT[C/T]GGTGCCAGTCTTTGT1877
rs756772875snpC/G3.98589e-050.00446406missense, intron-variant, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2234625CACCTGGAGGAGAAG[C/G]CGCACGTGTGCCAGT1877
rs756862223in-del-/Gintron-variantE4F1GRCh38.p716:2229370CCCTGGCCCGGGGGT[-/G]GAAGGGATTGGACTG1877
rs756869236snpC/T8.27712e-050.00643263utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variantE4F1, DNASE1L2GRCh38.p716:2235515CCTGGAGCATGCAGG[C/T]GAGCTGGTCATCGCC1877
rs756955653snpC/T1.73525e-050.0029455synonymous-codon, nc-transcript-variantE4F1GRCh38.p716:2228509CCTGCCACCACAGCG[C/T]TGCTGGGCCAGGAGG1877
rs757043640snpA/C1.68352e-050.00290126missense, nc-transcript-variantE4F1GRCh38.p716:2228456ACAAGATTCAGAAGG[A/C]CTGCCAGCGGGCCCC1877
rs757045675snpA/G/T8.46122e-050.00650383intron-variantE4F1GRCh38.p716:2232710CCTTGTCACCTTGTC[A/G/T]CCAGCCTGCTGGGGC1877
rs757113467snpA/C8.9658e-050.00669484intron-variantE4F1GRCh38.p716:2233867GGTGCTGGAGACCTT[A/C]CTGTGGTTCCCCAGC1877
rs757139134snpC/T7.07414e-050.0059469intron-variantE4F1GRCh38.p716:2232587CACGGGTGAGCTGGC[C/T]GCACCTCGGGCTGGA1877
rs757172853snpA/Gintron-variantE4F1GRCh38.p716:2224647CAAAAAAACAAAATT[A/G]GCCGGGCGTGGTGGC1877
rs757175068snpC/T9.11328e-050.00674967synonymous-codon, stop-gained, nc-transcript-variantE4F1GRCh38.p716:2223670GGCAGAAGCCCAGGC[C/T]GAAGCCGGGCGGGAA1877
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