| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs757203343 | snp | C/T | 3.10824e-05 | 0.00394211 | intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234983 | CGTGGTAGCTGACAC[C/T]CAGGAGTATATCATC | 1877 |
| rs757261374 | snp | A/G | 2.11916e-05 | 0.00325505 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223632 | GAGGGCGCGATGGCA[A/G]TGCGGGTGACGGCCG | 1877 |
| rs757278572 | snp | A/G | 5.25297e-05 | 0.00512466 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233583 | CTGCTGCCGGGTCCA[A/G]TCCCCAGCCCCTGGC | 1877 |
| rs757398464 | snp | A/G | 6.63526e-05 | 0.0057595 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229632 | CATCGTGGTGGAGGC[A/G]GCCTCTCTGGCAGCA | 1877 |
| rs757447879 | snp | A/G | 0.000140111 | 0.00836873 | intron-variant | E4F1 | GRCh38.p7 | 16:2234131 | CGGCCTGGCGGGCCC[A/G]CGGGTGATGGGCTTG | 1877 |
| rs757488406 | snp | A/G | 1.66699e-05 | 0.00288698 | intron-variant | E4F1 | GRCh38.p7 | 16:2232922 | AGGTCAGCATGGTGC[A/G]GGCAGCTGCCTGGTC | 1877 |
| rs757494192 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221890 | GAGATCACGGCACTG[C/T]ACTCCAGCCTGGGCG | 1877 |
| rs757549249 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235624 | GGCAGAGGACTCTGA[A/G]CGCCCCACCCATGCC | 1877 |
| rs757595268 | snp | C/T | 3.8931e-05 | 0.0044118 | intron-variant, synonymous-codon | E4F1 | GRCh38.p7 | 16:2228340 | CCCAGCCTCCGCCTT[C/T]CCAGGCCCTGCTGAC | 1877 |
| rs757694388 | snp | G/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229484 | CACACCTCCACAGCT[G/T]TACACTGGCAGAGCC | 1877 |
| rs757711242 | snp | G/T | 3.44893e-05 | 0.00415252 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234193 | GCCGTTCGCCTGCGC[G/T]CAGTGTGGCAAGGCC | 1877 |
| rs757761284 | snp | G/T | 1.65831e-05 | 0.00287945 | intron-variant | E4F1 | GRCh38.p7 | 16:2228285 | CTCCTGGGGGAATCT[G/T]TTCTAGGGCTGGAGG | 1877 |
| rs757773572 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221582 | TATTTTTAGTAAAGA[C/T]GTAATTTTGCCATGT | 1877 |
| rs757793831 | in-del | -/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2233195 | AGAGGTGGGGGCGAC[-/G]GGGGGCCCCGGAGGG | 1877 |
| rs757801476 | snp | C/G | 1.74406e-05 | 0.00295296 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235278 | TAGCGCCGGCCACCA[C/G]ATCATCGTGCAGAAC | 1877 |
| rs757917390 | snp | A/G | 1.72003e-05 | 0.00293255 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232307 | GGCCCAGGTGAAGCT[A/G]CTGGTGAACAAGGAT | 1877 |
| rs757946895 | snp | A/G | 8.141e-05 | 0.00637953 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234715 | GGCGAGAAGCCGTTC[A/G]AGTGCTACAAGTGCG | 1877 |
| rs758005235 | snp | A/G | 7.56959e-05 | 0.0061516 | intron-variant | E4F1 | GRCh38.p7 | 16:2233234 | TCTTCTGCCTGCTCG[A/G]TGCCAGTCTTTGTTC | 1877 |
| rs758203892 | snp | C/T | 3.34213e-05 | 0.00408773 | intron-variant | E4F1 | GRCh38.p7 | 16:2229539 | TCTGGAGCATACAGA[C/T]GACTCCCCTGTTTTC | 1877 |
| rs758235332 | snp | C/G | 1.69046e-05 | 0.00290723 | intron-variant | E4F1 | GRCh38.p7 | 16:2232724 | CGCCAGCCTGCTGGG[C/G]CTGCCCGGGGCTGAC | 1877 |
| rs758242392 | snp | C/T | | | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234478 | CTTCCCTGCCTCCAC[C/T]ATGCTCAGTCTTGAC | 1877 |
| rs758366940 | snp | C/G/T | 0.000173244 | 0.00930574 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235431 | GGGCACTGTGCTTGC[C/G/T]GCCCGGGCAGGGACA | 1877 |
| rs758410740 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228618 | TGTGCAGCCGGTTCC[A/G]GGGGCCACGTGGGCG | 1877 |
| rs758531781 | snp | C/G | 2.12303e-05 | 0.00325802 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223637 | CGCGATGGCAGTGCG[C/G]GTGACGGCCGCTCAT | 1877 |
| rs758540723 | snp | A/G | 7.23964e-05 | 0.00601606 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223684 | CCGAAGCCGGGCGGG[A/G]AGCGGGCGAGGGTGC | 1877 |
| rs758617478 | snp | C/T | 1.69378e-05 | 0.00291009 | intron-variant | E4F1 | GRCh38.p7 | 16:2229715 | GGCCTGATAGACCTT[C/T]GTGGTTGGGGCCAGA | 1877 |
| rs758627188 | snp | C/G/T | 0.00040486 | 0.0142225 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232235 | AGACGGTGAGATGGC[C/G/T]GAGGCCCCGGGCAGC | 1877 |
| rs758845282 | snp | A/G | 1.66999e-05 | 0.00288958 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233031 | GGAGCTGGAGCTGCC[A/G]GCTTGGGGACAGCCA | 1877 |
| rs758885811 | snp | A/G | 8.38019e-05 | 0.00647255 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228419 | CAGGCAGAGTTCACC[A/G]CCTTGGAGGATTTTG | 1877 |
| rs758933957 | snp | A/T | 1.67452e-05 | 0.0028935 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234299 | GGGAAGCTCTACAAG[A/T]CCATTGCCCATGTGC | 1877 |
| rs758988511 | snp | A/C | 1.80023e-05 | 0.00300014 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235334 | TGGGCCCAGAGGCGG[A/C]TGCCGCCGACACCAT | 1877 |
| rs759014990 | snp | C/T | 1.77407e-05 | 0.00297826 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232560 | CTCACTCATCCGGCA[C/T]CACCGGCGGCACACG | 1877 |
| rs759022207 | snp | A/G | 1.69e-05 | 0.00290684 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234240 | TGCTCAAGAAGCACC[A/G]GGAGGTGCACGTGCG | 1877 |
| rs759103194 | snp | A/C | 4.25876e-05 | 0.00461433 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223622 | TTGCGACATGGAGGG[A/C]GCGATGGCAGTGCGG | 1877 |
| rs759135345 | snp | C/T | 2.17417e-05 | 0.00329703 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223657 | CGGCCGCTCATACGG[C/T]AGAAGCCCAGGCCGA | 1877 |
| rs759140744 | snp | G/T | 1.89838e-05 | 0.00308083 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235025 | GGGGCCCTGGGGCCG[G/T]GCTGGGACCCAGGGG | 1877 |
| rs759192749 | snp | C/T | 4.99205e-05 | 0.00499578 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229674 | CGCATCTGACCTTGT[C/T]GGTAAGCCGACTTCC | 1877 |
| rs759361650 | snp | C/T | 1.67562e-05 | 0.00289444 | intron-variant | E4F1 | GRCh38.p7 | 16:2232968 | GGACGCAGCCGCCAC[C/T]GGGGTGTGTGAGGGA | 1877 |
| rs759384762 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230039 | AACATCCACCAGGCA[C/T]CCACCAGAATGGCCC | 1877 |
| rs759474688 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229226 | TCTGCCGGATGTGGC[A/G]GGCTGGGACTGTGCC | 1877 |
| rs759574404 | in-del | -/C | 1.68601e-05 | 0.00290341 | intron-variant | E4F1 | GRCh38.p7 | 16:2229711 | CGCTGGCCTGATAGA[-/C]CTTCGTGGTTGGGGC | 1877 |
| rs759640164 | snp | C/T | 7.20643e-05 | 0.00600225 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228326 | CGGAGCCCTGGCTGC[C/T]CAGCCTCCGCCTTCC | 1877 |
| rs759705360 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227661 | ACAAGCATGAGCCAC[C/T]GCCCTAATTTTGTAT | 1877 |
| rs759727069 | snp | G/T | 0.000186724 | 0.0096606 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223905 | GATCTCGCGGGACCC[G/T]CACAGCCCTCCACGA | 1877 |
| rs759729102 | snp | A/G | 1.6566e-05 | 0.00287797 | intron-variant | E4F1 | GRCh38.p7 | 16:2232421 | CCCTCCTGTTCCCCC[A/G]GGAGGGCCCTGAGCT | 1877 |
| rs759931884 | snp | A/G | 4.63274e-05 | 0.00481264 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234597 | GAACGCACAGCAGGT[A/G]CACTTCAGGACACAC | 1877 |
| rs759971546 | snp | A/C/G | 0.000119142 | 0.00771746 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234685 | TCACTGGTGCGGCAC[A/C/G]TGCGACACCACACAG | 1877 |
| rs759972057 | in-del | -/C | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223078 | AACAGCTTCGCAGAG[-/C]CTACCCATGAGCCAT | 1877 |
| rs760095584 | snp | A/G | 1.76833e-05 | 0.00297344 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235465 | GGCACTGAACAGGCC[A/G]CTGTGACCATGGTGT | 1877 |
| rs760265782 | snp | A/G | 1.77024e-05 | 0.00297504 | intron-variant | E4F1 | GRCh38.p7 | 16:2232619 | CCCGGTAGCACCCCG[A/G]TGGTTGGCCCTGGGG | 1877 |
| rs760295013 | snp | A/T | 1.69112e-05 | 0.0029078 | intron-variant | E4F1 | GRCh38.p7 | 16:2234018 | TGGGTGTGTGGCCCA[A/T]GGCAGTGGATGGGCT | 1877 |
| rs760318402 | snp | A/G | 5.50615e-05 | 0.00524669 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223765 | CGGCGCCCTTCAGCG[A/G]GGAAGGTAACCGGGC | 1877 |
| rs760382740 | snp | A/G | 3.77522e-05 | 0.0043445 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233934 | ACCCATGTCCTCAGT[A/G]CAGTGAGACCTTCCC | 1877 |
| rs760412256 | snp | C/T | 2.20811e-05 | 0.00332266 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223663 | CTCATACGGCAGAAG[C/T]CCAGGCCGAAGCCGG | 1877 |
| rs760474969 | snp | A/C | 1.76661e-05 | 0.00297199 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235054 | GGCAGCCAAGGCTGA[A/C]CTCTGTCCTTCTGCC | 1877 |
| rs760502409 | snp | A/G/T | 3.39733e-05 | 0.00412137 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232211 | CGTGGCTGCTGAGGC[A/G/T]GAGCTGGGAGACGGT | 1877 |
| rs760648312 | snp | C/G | 6.64971e-05 | 0.00576577 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233075 | AGGCGAGCCTATAGA[C/G]ACTTCACCCGTGATT | 1877 |
| rs760682407 | snp | C/G | 1.67198e-05 | 0.0028913 | intron-variant | E4F1 | GRCh38.p7 | 16:2232994 | AGGGATCTTCACTCC[C/G]TCACTCCACCTTGAA | 1877 |
| rs760709312 | snp | A/G | 1.68513e-05 | 0.00290265 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228395 | GATGTGCACAGATGC[A/G]GCCGCTGCCAGGCAG | 1877 |
| rs760743261 | snp | C/T | 1.67447e-05 | 0.00289345 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234328 | GCGTGGCCACCGGCG[C/T]GTCCACTCAGACGAG | 1877 |
| rs760795331 | snp | A/C | 1.82968e-05 | 0.00302457 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232529 | AGCTCTGTGGGGCCT[A/C]CTTCCGCACCAAGGG | 1877 |
| rs760904825 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224428 | CATTCTCAAACCAGT[C/G]CTGACAGGTGGATGT | 1877 |
| rs760939454 | snp | A/G | 4.1389e-05 | 0.00454893 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228335 | GGCTGCCCAGCCTCC[A/G]CCTTCCCAGGCCCTG | 1877 |
| rs761050026 | snp | A/G | 4.26285e-05 | 0.00461654 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233532 | GCATCGTCCTTGAGC[A/G]CGCTGCTGGGGAGGA | 1877 |
| rs761148466 | snp | C/G | 7.69201e-05 | 0.00620114 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233475 | CCTGCTCCAGCGAGG[C/G]CAGCCGTGAGAACCT | 1877 |
| rs761150421 | snp | C/G | 0.000160707 | 0.00896257 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234805 | CGGTGGAGGTGGGAG[C/G]GGGAGGGGAGGGGGC | 1877 |
| rs761154900 | snp | C/G | 2.38683e-05 | 0.0034545 | utr-variant-5-prime, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223593 | TCGTAAATCCGCCAT[C/G]TTCCTGCGGCGCGTT | 1877 |
| rs761238373 | snp | C/T | 6.9752e-05 | 0.00590518 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234702 | GCGACACCACACAGG[C/T]GAGAAGCCGTTCAAG | 1877 |
| rs761246977 | in-del | -/CCCCCT | 8.30453e-05 | 0.00644327 | intron-variant | E4F1 | GRCh38.p7 | 16:2232404 | TGTGTGGGTGGCAGG[-/CCCCCT]CCTGTTCCCCCAGGA | 1877 |
| rs761401348 | snp | A/G | 1.76855e-05 | 0.00297362 | intron-variant | E4F1 | GRCh38.p7 | 16:2232595 | AGCTGGCCGCACCTC[A/G]GGCTGGAGCCCGGTA | 1877 |
| rs761402215 | snp | G/T | 1.66219e-05 | 0.00288283 | utr-variant-3-prime, stop-lost, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235572 | GACGGTCATCGTCTA[G/T]CATGAGGTCTGCGGG | 1877 |
| rs761437634 | snp | A/G | 8.20715e-05 | 0.00640539 | intron-variant | E4F1 | GRCh38.p7 | 16:2234034 | GGCAGTGGATGGGCT[A/G]TAGGTGGCCGGGGTG | 1877 |
| rs761440483 | snp | C/T | 1.67237e-05 | 0.00289164 | intron-variant | E4F1 | GRCh38.p7 | 16:2229525 | CTCTGAGAACTAACT[C/T]TGGAGCATACAGACG | 1877 |
| rs761551068 | snp | A/G | 2.644e-05 | 0.00363583 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223841 | GGCAGAGGCCCGGAT[A/G]GCCCGAGCTGCGGGC | 1877 |
| rs761640771 | snp | C/T | 0.000667278 | 0.0182536 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223785 | GGTAACCGGGCCGAC[C/T]CGGAGGGTGCGGCCG | 1877 |
| rs761692430 | snp | C/T | 0.000156623 | 0.008848 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233947 | GTGCAGTGAGACCTT[C/T]CCGACAGCAGCCACC | 1877 |
| rs761782296 | snp | A/G | 1.74005e-05 | 0.00294957 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235071 | TCTGTCCTTCTGCCC[A/G]TCTGCCCAGGCCACT | 1877 |
| rs761799045 | snp | C/G | 8.42268e-05 | 0.00648894 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232263 | AGCCCCCGCCAGCAG[C/G]GGCTGGGGCTCGCAG | 1877 |
| rs761819706 | snp | A/G | 6.64717e-05 | 0.00576467 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233085 | ATAGAGACTTCACCC[A/G]TGATTCACCTGGTGA | 1877 |
| rs761884575 | snp | A/G | 1.77115e-05 | 0.00297581 | intron-variant | E4F1 | GRCh38.p7 | 16:2233190 | GCCCCAGAGGTGGGG[A/G]CGACGGGGGGCCCCG | 1877 |
| rs761940497 | snp | C/G | | | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228484 | CCCTCCGGAGGCCCT[C/G]CCTGCCACCCCTGCC | 1877 |
| rs762006272 | snp | C/G | 6.54429e-05 | 0.00571989 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234568 | CCAGGCTGGCACTGA[C/G]AGGTGTCTCCACAGA | 1877 |
| rs762096053 | snp | A/C/G | 5.02595e-05 | 0.00501275 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234341 | CGCGTCCACTCAGAC[A/C/G]AGCGGCCCTACCCTT | 1877 |
| rs762148707 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235924 | CATTGGCATGTTGAC[C/T]AACAGCCTCCTGCCC | 1877 |
| rs762184429 | snp | A/G | 1.67722e-05 | 0.00289583 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228409 | CGGCCGCTGCCAGGC[A/G]GAGTTCACCGCCTTG | 1877 |
| rs762194932 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225958 | ATTAGCTGGCCGTGG[C/T]GGCAGGCGCCTGTAG | 1877 |
| rs762199460 | snp | C/T | 1.78969e-05 | 0.00299135 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232545 | CTTCCGCACCAAGGG[C/T]TCACTCATCCGGCAC | 1877 |
| rs762224938 | in-del | -/TG | 1.77084e-05 | 0.00297554 | utr-variant-3-prime, frameshift-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235467 | CACTGAACAGGCCAC[-/TG]TGACCATGGTGTCAT | 1877 |
| rs762241508 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224239 | GAGCCTAGTGCAAGA[A/G]GGCTGGTGCACTGCA | 1877 |
| rs762287426 | snp | A/G | 4.10408e-05 | 0.00452976 | intron-variant | E4F1 | GRCh38.p7 | 16:2232442 | GCCCTGAGCTGCCAC[A/G]CCCTCCCCCACAGGG | 1877 |
| rs762289883 | snp | A/G | 5.00471e-05 | 0.00500211 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234941 | CCTCACGGAAGACCC[A/G]CACACAGTGTTGGTG | 1877 |
| rs762313154 | in-del | -/GA | 1.67385e-05 | 0.00289292 | intron-variant | E4F1 | GRCh38.p7 | 16:2232978 | GCCACTGGGGTGTGT[-/GA]GGGATCTTCACTCCC | 1877 |
| rs762331438 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222895 | GGCGTGGTGGCGGAC[A/G]CCTGTAGTCCCAGCT | 1877 |
| rs762373026 | snp | A/G | 5.25887e-05 | 0.00512753 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233540 | CTTGAGCGCGCTGCT[A/G]GGGAGGAGGGTGCCC | 1877 |
| rs762455232 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230290 | TGATGTGCTGTGGGA[A/G]GGGCTGTTGCGAGGT | 1877 |
| rs762538116 | snp | C/G | 0.000309741 | 0.0124409 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234825 | GGGGAGGGGGCCGGG[C/G]CTTGCCTAGCCCTGA | 1877 |
| rs762554231 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224045 | CCCGGTGTAGACATT[C/G]GCAGACGCCGGCGTC | 1877 |
| rs762559737 | snp | G/T | 3.1875e-05 | 0.00399206 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235583 | TCTAGCATGAGGTCT[G/T]CGGGGTCCTGGCCGG | 1877 |
| rs762568774 | snp | C/G | 1.66205e-05 | 0.00288271 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229668 | CAGCCACGCATCTGA[C/G]CTTGTTGGTAAGCCG | 1877 |
| rs762585673 | snp | A/G | 8.31635e-05 | 0.00644786 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232899 | GTCAGCAAAGAGGAC[A/G]CACGTGCAGGTCAGC | 1877 |
| rs762673876 | snp | A/G | 3.6268e-05 | 0.00425825 | intron-variant | E4F1 | GRCh38.p7 | 16:2234167 | ATGCTGTGTGTGGCT[A/G]CAGGGCCGAGGCCGT | 1877 |
| rs762686209 | snp | A/G | 1.65853e-05 | 0.00287964 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229609 | GAGGAGCCCATCACT[A/G]TGGCCCACATCGTGG | 1877 |
| rs762846183 | snp | A/G | 1.75065e-05 | 0.00295854 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235256 | TGCAGCAGATCGTGC[A/G]CCAGGCTAGCGCCGG | 1877 |
| rs762872180 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231584 | GCACATTGTCAGATT[C/T]TTCCCAGCATCCTCC | 1877 |
| rs762886773 | snp | A/G | 9.80248e-05 | 0.0070002 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223792 | GGGCCGACCCGGAGG[A/G]TGCGGCCGGGGTGCG | 1877 |
| rs762912940 | snp | A/G | 2.0354e-05 | 0.00319007 | intron-variant | E4F1 | GRCh38.p7 | 16:2234125 | GGCAGGCGGCCTGGC[A/G]GGCCCGCGGGTGATG | 1877 |
| rs762939643 | snp | A/G | 5.48787e-05 | 0.00523797 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223846 | AGGCCCGGATGGCCC[A/G]AGCTGCGGGCTCGAC | 1877 |
| rs763007895 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228112 | TCCCTGCAGCCTAAG[C/T]GTGCTGTCAGGGCCA | 1877 |
| rs763064106 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228665 | CTGGCTGCGGTGTGG[A/G]AGGGTCCGGGTGTGT | 1877 |
| rs763064601 | snp | C/G | 1.86851e-05 | 0.0030565 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232349 | GTGTGCGCTGTGCCA[C/G]AAGACCTTCAAGACG | 1877 |
| rs763160615 | snp | C/T | 3.16211e-05 | 0.00397612 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233443 | TCCCCTGCAGCCCCC[C/T]GTCTCCCAGGAGCTC | 1877 |
| rs763236508 | snp | C/T | 1.67702e-05 | 0.00289566 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234354 | ACGAGCGGCCCTACC[C/T]TTGTCCCAAGTGTGG | 1877 |
| rs763251259 | snp | A/G | 0.0010313 | 0.0226845 | intron-variant | E4F1 | GRCh38.p7 | 16:2228556 | CCCCCATCCCCTCCC[A/G]GGTTCACCTGACAGG | 1877 |
| rs763572955 | snp | A/G | 3.56278e-05 | 0.0042205 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235470 | TGAACAGGCCACTGT[A/G]ACCATGGTGTCATCA | 1877 |
| rs763701964 | snp | C/T | 4.99089e-05 | 0.00499519 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232797 | TGTGGAAAGAGCTTC[C/T]GGGAGTCGGGTGCAC | 1877 |
| rs763791867 | snp | A/G | 7.08015e-05 | 0.00594943 | intron-variant | E4F1 | GRCh38.p7 | 16:2232622 | GGTAGCACCCCGATG[A/G]TTGGCCCTGGGGTGC | 1877 |
| rs763870651 | snp | C/T | 4.09526e-05 | 0.00452489 | intron-variant, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234970 | TGGAGTTCTCGTCCG[C/T]GGTAGCTGACACCCA | 1877 |
| rs763880051 | snp | C/T | 3.78652e-05 | 0.00435099 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233935 | CCCATGTCCTCAGTG[C/T]AGTGAGACCTTCCCG | 1877 |
| rs763883207 | snp | C/T | 2.21403e-05 | 0.00332711 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223664 | TCATACGGCAGAAGC[C/T]CAGGCCGAAGCCGGG | 1877 |
| rs763968295 | snp | C/T | 3.36927e-05 | 0.00410429 | intron-variant | E4F1 | GRCh38.p7 | 16:2233856 | AGCCTGCCCCGGGTG[C/T]TGGAGACCTTCCTGT | 1877 |
| rs763977249 | snp | A/C | 4.24214e-05 | 0.00460531 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223626 | GACATGGAGGGCGCG[A/C]TGGCAGTGCGGGTGA | 1877 |
| rs763978552 | snp | G/T | 1.66211e-05 | 0.00288275 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233078 | CGAGCCTATAGAGAC[G/T]TCACCCGTGATTCAC | 1877 |
| rs764007666 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224564 | GGAGGTCGAGACGGG[C/T]GGGTCACGAGGTCAG | 1877 |
| rs764273831 | snp | C/T | 2.03764e-05 | 0.00319183 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228336 | GCTGCCCAGCCTCCG[C/T]CTTCCCAGGCCCTGC | 1877 |
| rs764322081 | snp | C/G/T | 3.35685e-05 | 0.00409674 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234277 | CCGCTTCCGCTGTGG[C/G/T]GACTGCGGGAAGCTC | 1877 |
| rs764338337 | snp | C/T | 3.36712e-05 | 0.00410298 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228398 | GTGCACAGATGCGGC[C/T]GCTGCCAGGCAGAGT | 1877 |
| rs764363317 | snp | G/T | 2.05789e-05 | 0.00320765 | intron-variant | E4F1 | GRCh38.p7 | 16:2232437 | GGAGGGCCCTGAGCT[G/T]CCACGCCCTCCCCCA | 1877 |
| rs764444519 | snp | G/T | 3.4856e-05 | 0.00417454 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235320 | CGAGGAGACGGCGCT[G/T]GGCCCAGAGGCGGCT | 1877 |
| rs764511931 | snp | C/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221816 | TACAAAAATTAGCTA[C/G]TGATGGGCACCTGTA | 1877 |
| rs764511982 | snp | A/G | 1.73171e-05 | 0.00294249 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235089 | TGCCCAGGCCACTGC[A/G]GACGATGCGGAGACC | 1877 |
| rs764575994 | in-del | -/A | 1.65608e-05 | 0.00287752 | intron-variant | E4F1 | GRCh38.p7 | 16:2232602 | CGCACCTCGGGCTGG[-/A]GCCCGGTAGCACCCC | 1877 |
| rs764612488 | snp | G/T | 1.99651e-05 | 0.00315945 | intron-variant | E4F1 | GRCh38.p7 | 16:2232376 | GACGGTGAGCCGGCG[G/T]GCGGGGAGCCAGTGT | 1877 |
| rs764615401 | snp | A/G | 0.000101586 | 0.00712621 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234812 | GGTGGGAGGGGGAGG[A/G]GAGGGGGCCGGGGCT | 1877 |
| rs764625945 | snp | C/G | 0.000146295 | 0.00855138 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233478 | GCTCCAGCGAGGGCA[C/G]CCGTGAGAACCTGCT | 1877 |
| rs764709853 | snp | A/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222732 | TAAATTTTAAAAAAT[A/T]TAAAAAGTGGCTGGG | 1877 |
| rs764715204 | snp | A/G | 7.24244e-05 | 0.00601722 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234708 | CCACACAGGCGAGAA[A/G]CCGTTCAAGTGCTAC | 1877 |
| rs764936663 | snp | G/T | 3.34426e-05 | 0.00408903 | intron-variant | E4F1 | GRCh38.p7 | 16:2229528 | TGAGAACTAACTCTG[G/T]AGCATACAGACGACT | 1877 |
| rs764947330 | in-del | -/GGGGGCGACG | 1.75243e-05 | 0.00296004 | splice-donor-variant | E4F1 | GRCh38.p7 | 16:2233185 | CCTGGCCCCAGAGGT[-/GGGGGCGACG]GGGGGCGACGGGGGG | 1877 |
| rs765015745 | snp | C/T | 0.000158926 | 0.00891278 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233949 | GCAGTGAGACCTTCC[C/T]GACAGCAGCCACCCT | 1877 |
| rs765020785 | snp | G/T | 1.66181e-05 | 0.00288249 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232808 | CTTCCGGGAGTCGGG[G/T]GCACTGACCCGGCAC | 1877 |
| rs765067306 | snp | C/G | 2.03126e-05 | 0.00318683 | intron-variant | E4F1 | GRCh38.p7 | 16:2234122 | GGTGGCAGGCGGCCT[C/G]GCGGGCCCGCGGGTG | 1877 |
| rs765107376 | snp | A/C | 1.73839e-05 | 0.00294816 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235073 | TGTCCTTCTGCCCAT[A/C]TGCCCAGGCCACTGC | 1877 |
| rs765140149 | snp | A/G | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232264 | GCCCCCGCCAGCAGG[A/G]GCTGGGGCTCGCAGG | 1877 |
| rs765165792 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230144 | CTTGCTGCTGGCCGT[A/G]GCCTGCCCTCCCCAG | 1877 |
| rs765209050 | snp | A/G | 2.28053e-05 | 0.0033767 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223671 | GCAGAAGCCCAGGCC[A/G]AAGCCGGGCGGGAAG | 1877 |
| rs765280928 | snp | G/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2223421 | CCGCCCCATCTTCGC[G/T]CTCAGCGCGCCCGGC | 1877 |
| rs765357279 | snp | G/T | 0.000118517 | 0.00769703 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232221 | GAGGCGGAGCTGGGA[G/T]ACGGTGAGATGGCCG | 1877 |
| rs765492789 | snp | A/G | 1.72157e-05 | 0.00293386 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235378 | CCCGAGAGCCTGACA[A/G]AGCAGGTGGCCATGA | 1877 |
| rs765497258 | snp | C/T | 1.66203e-05 | 0.00288268 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233093 | TTCACCCGTGATTCA[C/T]CTGGTGACAGATGCC | 1877 |
| rs765598650 | snp | C/T | 0.000255904 | 0.0113087 | intron-variant | E4F1 | GRCh38.p7 | 16:2233204 | GGCGACGGGGGGCCC[C/T]GGAGGGCTGCTCTGT | 1877 |
| rs765658838 | snp | G/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221618 | TGCTTGGTCTTGAAC[G/T]CCTGATGTCAGGTGA | 1877 |
| rs765687917 | snp | C/T | 1.78554e-05 | 0.00298787 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232547 | TCCGCACCAAGGGCT[C/T]ACTCATCCGGCACCA | 1877 |
| rs765688041 | snp | C/T | 1.93272e-05 | 0.00310857 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228341 | CCAGCCTCCGCCTTC[C/T]CAGGCCCTGCTGACA | 1877 |
| rs765717108 | in-del | -/CAT | 5.36466e-05 | 0.00517885 | cds-indel, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235473 | ACAGGCCACTGTGAC[-/CAT]GGTGTCATCAGAGGA | 1877 |
| rs765751881 | in-del | -/C | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226345 | CTGGGGTAGGGGGTT[-/C]TTCAGTGGCAATGCC | 1877 |
| rs765775917 | snp | A/C | 2.02112e-05 | 0.00317887 | intron-variant | E4F1 | GRCh38.p7 | 16:2232449 | GCTGCCACGCCCTCC[A/C]CCACAGGGCAGCATC | 1877 |
| rs765789830 | snp | A/G | 5.54001e-05 | 0.00526279 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233542 | TGAGCGCGCTGCTGG[A/G]GAGGAGGGTGCCCTG | 1877 |
| rs765811587 | snp | A/C | 0.000211484 | 0.0102809 | intron-variant | E4F1 | GRCh38.p7 | 16:2233690 | CTCCCAGGGCTGGAT[A/C]CCAGGGGCTGTCCCC | 1877 |
| rs765904296 | snp | C/G | 3.3248e-05 | 0.00407712 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229669 | AGCCACGCATCTGAC[C/G]TTGTTGGTAAGCCGA | 1877 |
| rs765920788 | in-del | -/CTGCTCTGTCTTCTGC | 1.83656e-05 | 0.00303026 | intron-variant | E4F1 | GRCh38.p7 | 16:2233210 | GGGGGCCCCGGAGGG[-/CTGCTCTGTCTTCTGC]CTGCTCTGTCTTCTG | 1877 |
| rs765998701 | snp | C/G | 4.39638e-05 | 0.00468828 | utr-variant-5-prime, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223610 | TCCTGCGGCGCGTTG[C/G]GACATGGAGGGCGCG | 1877 |
| rs766241828 | snp | C/T | 0.00022589 | 0.0106252 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235584 | CTAGCATGAGGTCTG[C/T]GGGGTCCTGGCCGGG | 1877 |
| rs766244863 | snp | C/G/T | 0.000767158 | 0.0195704 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234174 | GTGTGGCTGCAGGGC[C/G/T]GAGGCCGTTCGCCTG | 1877 |
| rs766282377 | snp | C/G | 0.000185856 | 0.00963813 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223852 | GGATGGCCCGAGCTG[C/G]GGGCTCGACCGACCC | 1877 |
| rs766330975 | snp | A/G | 1.662e-05 | 0.00288266 | intron-variant | E4F1 | GRCh38.p7 | 16:2234126 | GCAGGCGGCCTGGCG[A/G]GCCCGCGGGTGATGG | 1877 |
| rs766333148 | snp | A/C | 0.000105005 | 0.00724511 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235257 | GCAGCAGATCGTGCA[A/C]CAGGCTAGCGCCGGC | 1877 |
| rs766423032 | snp | A/G | 1.77162e-05 | 0.0029762 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235171 | GCAGGCGGGGGCGGG[A/G]AGGCTCCCTGGCACA | 1877 |
| rs766436358 | snp | A/C | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228996 | TGAACCCCGCACACG[A/C]CGCAGCGGGCGCTTG | 1877 |
| rs766567991 | snp | A/G | 1.89421e-05 | 0.00307745 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232360 | GCCACAAGACCTTCA[A/G]GACGGTGAGCCGGCG | 1877 |
| rs766620867 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225986 | TAGTCACAGCTTCTC[A/G]GGAGGCTGAGGCAGG | 1877 |
| rs766636641 | snp | C/T | 1.6582e-05 | 0.00287936 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234587 | TGTCTCCACAGAACG[C/T]ACAGCAGGTGCACTT | 1877 |
| rs766728312 | snp | A/C | 1.74857e-05 | 0.00295678 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235452 | GGCAGGGACAAGTGG[A/C]ACTGAACAGGCCACT | 1877 |
| rs766755916 | in-del | -/A | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225791 | CAGTCTCTGTTTAGG[-/A]AAAAAAAAAAAAAAA | 1877 |
| rs766785583 | snp | C/G | 1.66385e-05 | 0.00288426 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233064 | TCATCGGTGACAGGC[C/G]AGCCTATAGAGACTT | 1877 |
| rs766832827 | snp | A/C | 1.66446e-05 | 0.00288479 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233116 | CAGATGCCAAGGGCA[A/C]CGTCATCCACGAAGT | 1877 |
| rs766839471 | snp | C/T | 1.68309e-05 | 0.00290089 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234374 | CCCAAGTGTGGCAAG[C/T]GCTACAAGACTAAGG | 1877 |
| rs766917187 | snp | G/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231933 | TGGACACATTTAGGG[G/T]CCCTGGAGCATCTCT | 1877 |
| rs766918056 | snp | G/T | 1.67508e-05 | 0.00289398 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228435 | CCTTGGAGGATTTTG[G/T]TCAGCACAAGATTCA | 1877 |
| rs766927884 | snp | A/G | 1.77486e-05 | 0.00297892 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232565 | TCATCCGGCACCACC[A/G]GCGGCACACGGGTGA | 1877 |
| rs766928474 | in-del | -/C | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224880 | CAGCCCCTTTAACTT[-/C]CGGGCTCTGCTGCCT | 1877 |
| rs766961962 | snp | C/T | 3.54773e-05 | 0.00421158 | intron-variant | E4F1 | GRCh38.p7 | 16:2232617 | AGCCCGGTAGCACCC[C/T]GATGGTTGGCCCTGG | 1877 |
| rs767053981 | snp | C/T | 0.000416611 | 0.0144268 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233927 | AGGACCCACCCATGT[C/T]CTCAGTGCAGTGAGA | 1877 |
| rs767227504 | snp | C/T | 1.69562e-05 | 0.00291167 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233561 | GAGGGTGCCCTGGAG[C/T]CAGCTCCTGCTGCCG | 1877 |
| rs767254229 | snp | A/G | 2.12709e-05 | 0.00326114 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223623 | TGCGACATGGAGGGC[A/G]CGATGGCAGTGCGGG | 1877 |
| rs767305927 | snp | C/T | 1.65858e-05 | 0.00287969 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229617 | CATCACTGTGGCCCA[C/T]ATCGTGGTGGAGGCG | 1877 |
| rs767312846 | snp | C/T | 5.1839e-05 | 0.00509086 | intron-variant, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234964 | TGTTGGTGGAGTTCT[C/T]GTCCGTGGTAGCTGA | 1877 |
| rs767358936 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226549 | ACATTTGCCCAGCTC[C/T]TTCGGGCATCAGGCC | 1877 |
| rs767394997 | snp | A/G | 0.000240674 | 0.0109672 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234898 | AGTTGCTGGTGTCTG[A/G]GGACAGCCCCGCGGC | 1877 |
| rs767396342 | snp | A/G | 1.67323e-05 | 0.00289239 | intron-variant | E4F1 | GRCh38.p7 | 16:2232981 | ACTGGGGTGTGTGAG[A/G]GATCTTCACTCCCTC | 1877 |
| rs767398028 | snp | A/G | 8.41248e-05 | 0.00648501 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234264 | ACGTGCGTGAGCGCC[A/G]CTTCCGCTGTGGCGA | 1877 |
| rs767474828 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228134 | TCAGGGCCACCCTCT[A/G]CTGGGTGCTGACCTC | 1877 |
| rs767493337 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233988 | ACAAGAGGGGCCACA[C/T]CGGTAGGTGATGGGT | 1877 |
| rs767715963 | snp | A/G | 2.26894e-05 | 0.00336811 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228329 | AGCCCTGGCTGCCCA[A/G]CCTCCGCCTTCCCAG | 1877 |
| rs767738531 | snp | C/T | 2.07648e-05 | 0.0032221 | intron-variant | E4F1 | GRCh38.p7 | 16:2232429 | TTCCCCCAGGAGGGC[C/T]CTGAGCTGCCACGCC | 1877 |
| rs767807563 | snp | C/T | 0.000196367 | 0.00990682 | intron-variant | E4F1 | GRCh38.p7 | 16:2223941 | CCAGGTTTGCTGCGA[C/T]CCTCACGGGCCTCTC | 1877 |
| rs767987436 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230663 | GGCGGAGGCCAACCC[A/G]GGGCCTGGGAAGGGC | 1877 |
| rs767987855 | snp | A/G | 1.70988e-05 | 0.00292389 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232297 | AGGGTGAGCAGGCCC[A/G]GGTGAAGCTACTGGT | 1877 |
| rs768046902 | snp | A/G | 4.24565e-05 | 0.00460722 | synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234606 | GCAGGTGCACTTCAG[A/G]ACACACCTGGAGGAG | 1877 |
| rs768127478 | snp | C/T | 6.16998e-05 | 0.00555393 | intron-variant | E4F1 | GRCh38.p7 | 16:2228568 | CCCGGGTTCACCTGA[C/T]AGGTGGGGGAGGTGG | 1877 |
| rs768181595 | snp | C/T | 5.50494e-05 | 0.00524611 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228294 | GAATCTGTTCTAGGG[C/T]TGGAGGAAAAGCCAG | 1877 |
| rs768236399 | snp | A/G | 1.75835e-05 | 0.00296504 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235156 | GAGGTGAGGGGTAGG[A/G]CAGGCGGGGGCGGGG | 1877 |
| rs768267492 | snp | C/T | 5.05331e-05 | 0.00502633 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223836 | GGGCTGGCAGAGGCC[C/T]GGATGGCCCGAGCTG | 1877 |
| rs768276260 | snp | G/T | 1.86014e-05 | 0.00304965 | intron-variant | E4F1 | GRCh38.p7 | 16:2234153 | ATGGGCTTGGCCTGA[G/T]GCTGTGTGTGGCTGC | 1877 |
| rs768293353 | snp | G/T | 1.76403e-05 | 0.00296982 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235219 | GTGGCCCTGCAGGTG[G/T]ACAGCCACATCATGA | 1877 |
| rs768327316 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225071 | TACAAAAATTAGCTG[C/G]GCGTGGTGGTGCGCG | 1877 |
| rs768338851 | snp | A/G | 4.55218e-05 | 0.00477062 | intron-variant | E4F1 | GRCh38.p7 | 16:2233400 | GGTGCTGGATGCCAG[A/G]CTGCCTGGCCAGCCT | 1877 |
| rs768355623 | snp | G/T | 5.74828e-05 | 0.00536079 | stop-gained, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223767 | GCGCCCTTCAGCGAG[G/T]AAGGTAACCGGGCCG | 1877 |
| rs768357528 | snp | A/G | 1.752e-05 | 0.00295968 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232321 | TACTGGTGAACAAGG[A/G]TGGCCGCTATGTGTG | 1877 |
| rs768376283 | snp | A/G | 7.17592e-05 | 0.00598953 | intron-variant | E4F1 | GRCh38.p7 | 16:2234020 | GGTGTGTGGCCCATG[A/G]CAGTGGATGGGCTAT | 1877 |
| rs768428620 | snp | G/T | 8.35492e-05 | 0.00646279 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234647 | TGTGCCAGTTCTGCA[G/T]CCGTGGCTTCCGAGA | 1877 |
| rs768589395 | snp | A/G | 1.73264e-05 | 0.00294328 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233180 | GAAAGCCCTGGCCCC[A/G]GAGGTGGGGGCGACG | 1877 |
| rs768604168 | snp | A/G | 5.0234e-05 | 0.00501144 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234329 | CGTGGCCACCGGCGC[A/G]TCCACTCAGACGAGC | 1877 |
| rs768677416 | snp | C/G | 6.81454e-05 | 0.00583679 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234558 | GTGGCCAAGGCCAGG[C/G]TGGCACTGACAGGTG | 1877 |
| rs768710169 | snp | C/T | 1.82168e-05 | 0.00301795 | intron-variant | E4F1 | GRCh38.p7 | 16:2228535 | GGAGGTGAGCCCTCA[C/T]CCACTCCCCCATCCC | 1877 |
| rs768841755 | snp | C/G/T | 5.20913e-05 | 0.00510327 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235435 | ACTGTGCTTGCCGCC[C/G/T]GGGCAGGGACAAGTG | 1877 |
| rs768941186 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2229766 | GTATGCTCGTCTCTC[C/T]CGAGACCAGGGCCTG | 1877 |
| rs769167141 | snp | C/T | 2.12909e-05 | 0.00326266 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223645 | CAGTGCGGGTGACGG[C/T]CGCTCATACGGCAGA | 1877 |
| rs769184164 | in-del | -/C | 0.000119353 | 0.00772414 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234905 | GGTGTCTGAGGACAG[-/C]CCCGCGGCAGCCACC | 1877 |
| rs769258837 | snp | A/C | 1.74912e-05 | 0.00295725 | intron-variant | E4F1 | GRCh38.p7 | 16:2232135 | GTCTCTGGACAGGGG[A/C]AGGTCCTGGGGCTTA | 1877 |
| rs769258902 | snp | C/T | 2.3186e-05 | 0.00340477 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223600 | TCCGCCATCTTCCTG[C/T]GGCGCGTTGCGACAT | 1877 |
| rs769346974 | snp | A/G | 1.66123e-05 | 0.00288199 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229662 | AGACATCAGCCACGC[A/G]TCTGACCTTGTTGGT | 1877 |
| rs769352548 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223897 | ACCTCGCGGATCTCG[C/T]GGGACCCTCACAGCC | 1877 |
| rs769397200 | snp | A/C | 3.74146e-05 | 0.00432503 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228310 | TGGAGGAAAAGCCAG[A/C]CGGAGCCCTGGCTGC | 1877 |
| rs769475965 | snp | A/G | 1.73993e-05 | 0.00294947 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235300 | GTGCAGAACGTCACC[A/G]TGGACGAGGAGACGG | 1877 |
| rs769485429 | snp | C/T | 2.07119e-05 | 0.003218 | intron-variant | E4F1 | GRCh38.p7 | 16:2232405 | GTGTGGGTGGCAGGC[C/T]CCCTCCTGTTCCCCC | 1877 |
| rs769614432 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2232392 | GCGGGGAGCCAGTGT[A/G]TGGGTGGCAGGCCCC | 1877 |
| rs769646478 | snp | A/G | 2.66756e-05 | 0.00365199 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223842 | GCAGAGGCCCGGATG[A/G]CCCGAGCTGCGGGCT | 1877 |
| rs769735039 | snp | A/G | 1.65116e-05 | 0.00287324 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232340 | CCGCTATGTGTGTGC[A/G]CTGTGCCACAAGACC | 1877 |
| rs769794229 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231387 | GAGCGTGTAAGGGCT[C/T]GGGCAGGAGAGGCTC | 1877 |
| rs769810472 | snp | C/G | 5.17505e-05 | 0.00508651 | missense, splice-donor-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233502 | ACCTGCTGCACCAGG[C/G]CATGCAGAACTCCGG | 1877 |
| rs769848198 | snp | A/G | 2.13842e-05 | 0.00326981 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235522 | CATGCAGGCGAGCTG[A/G]TCATCGCCTCGCCGG | 1877 |
| rs769898047 | snp | G/T | 3.58455e-05 | 0.00423338 | intron-variant | E4F1 | GRCh38.p7 | 16:2233433 | TCTCTCTGCCTCCCC[G/T]GCAGCCCCCCGTCTC | 1877 |
| rs769986330 | snp | A/G | 9.18907e-05 | 0.00677768 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234659 | GCAGCCGTGGCTTCC[A/G]AGAGAAGGGCTCACT | 1877 |
| rs770015821 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227979 | CCAGCAGTCTTAAAT[C/T]CTGGTCCTTTACTGT | 1877 |
| rs770063253 | snp | A/G | 1.67722e-05 | 0.00289583 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232762 | TCTCTGCAGATGAGC[A/G]CCCCTACAAGTGCTC | 1877 |
| rs770079145 | snp | A/G | 6.16162e-05 | 0.00555016 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234573 | CTGGCACTGACAGGT[A/G]TCTCCACAGAACGCA | 1877 |
| rs770111206 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230120 | CCCGCCTCTCTAGCT[A/G]GGCTCGGACTTGCTG | 1877 |
| rs770147687 | snp | A/G | 8.75159e-05 | 0.0066144 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233905 | CAGCGAGGCCTCAGC[A/G]GTGCCCAGGACCCAC | 1877 |
| rs770203028 | snp | C/T | 4.85779e-05 | 0.00492814 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233986 | CCACAAGAGGGGCCA[C/T]ACCGGTAGGTGATGG | 1877 |
| rs770485404 | snp | C/T | 3.41175e-05 | 0.00413008 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232193 | GCACATCAAAGAGGT[C/T]ATCGTGGCTGCTGAG | 1877 |
| rs770486015 | snp | A/C/G | 6.47359e-05 | 0.00568898 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223655 | GACGGCCGCTCATAC[A/C/G]GCAGAAGCCCAGGCC | 1877 |
| rs770518103 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2233707 | CAGGGGCTGTCCCCA[C/T]GCTGGCCTTCGCCTC | 1877 |
| rs770621423 | snp | C/T | 1.67424e-05 | 0.00289326 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234314 | ACCATTGCCCATGTG[C/T]GTGGCCACCGGCGCG | 1877 |
| rs770654268 | snp | A/G | 1.70075e-05 | 0.00291607 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228380 | GTTGCAGATGAGGAC[A/G]ATGTGCACAGATGCG | 1877 |
| rs770709408 | snp | A/G | 1.74248e-05 | 0.00295163 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235354 | GCCGACACCATCACC[A/G]TCGCCACCCCCGAGA | 1877 |
| rs770711229 | snp | A/G | 1.68459e-05 | 0.00290219 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234257 | GAGGTGCACGTGCGT[A/G]AGCGCCGCTTCCGCT | 1877 |
| rs770836717 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222794 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 1877 |
| rs770867398 | snp | A/G | 0.000137826 | 0.00830026 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228312 | GAGGAAAAGCCAGAC[A/G]GAGCCCTGGCTGCCC | 1877 |
| rs770990600 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230026 | GCCCGTAGGCAGCAA[C/T]ATCCACCAGGCACCC | 1877 |
| rs771047849 | snp | A/C | 4.1772e-05 | 0.00456993 | intron-variant | E4F1 | GRCh38.p7 | 16:2232416 | AGGCCCCCTCCTGTT[A/C]CCCCAGGAGGGCCCT | 1877 |
| rs771099882 | snp | A/G | 5.04096e-05 | 0.00502018 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235622 | AGGGCAGAGGACTCT[A/G]AGCGCCCCACCCATG | 1877 |
| rs771120204 | in-del | -/CCTGCCACC | 3.42416e-05 | 0.00413759 | cds-indel, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228485 | CCTCCGGAGGCCCTG[-/CCTGCCACC]CCTGCCACCACAGCG | 1877 |
| rs771142053 | snp | A/G | 5.97818e-05 | 0.00546693 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233516 | GCCATGCAGAACTCC[A/G]GCATCGTCCTTGAGC | 1877 |
| rs771297738 | snp | C/G | 1.94638e-05 | 0.00311954 | intron-variant | E4F1 | GRCh38.p7 | 16:2228558 | CCCATCCCCTCCCGG[C/G]TTCACCTGACAGGTG | 1877 |
| rs771304579 | snp | A/G | 3.3437e-05 | 0.00408869 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232772 | TGAGCGCCCCTACAA[A/G]TGCTCCAAGTGTGGA | 1877 |
| rs771316256 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2232407 | GTGGGTGGCAGGCCC[C/T]CTCCTGTTCCCCCAG | 1877 |
| rs771408875 | snp | C/T | 2.16261e-05 | 0.00328825 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223819 | TGCGGGCAGTTCATC[C/T]CGGGCTGGCAGAGGC | 1877 |
| rs771449272 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228545 | CCTCACCCACTCCCC[C/T]ATCCCCTCCCGGGTT | 1877 |
| rs771526015 | snp | A/G | 3.84682e-05 | 0.0043855 | intron-variant | E4F1 | GRCh38.p7 | 16:2234142 | GCCCGCGGGTGATGG[A/G]CTTGGCCTGATGCTG | 1877 |
| rs771618296 | snp | C/T | 1.67531e-05 | 0.00289418 | intron-variant | E4F1 | GRCh38.p7 | 16:2233999 | CACACCGGTAGGTGA[C/T]GGGTGGGTGTGTGGC | 1877 |
| rs771633885 | snp | C/T | 4.5609e-05 | 0.00477519 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223748 | CGGCTTCCTCGGCCT[C/T]CCGGCGCCCTTCAGC | 1877 |
| rs771680213 | snp | A/G | 1.68301e-05 | 0.00290082 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232244 | GATGGCCGAGGCCCC[A/G]GGCAGCCCCCGCCAG | 1877 |
| rs771704183 | snp | C/T | 3.46344e-05 | 0.00416125 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235125 | GGCCACGGAGATCAT[C/T]GAGGGCACCCAGACA | 1877 |
| rs771770063 | snp | A/G | 1.70003e-05 | 0.00291545 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233159 | GCAGGAGCTGTCCCT[A/G]GGCATGAAAGCCCTG | 1877 |
| rs771770366 | snp | A/C | 3.56691e-05 | 0.00422294 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234428 | GGCGCCTGATCCCCC[A/C]ATCCTGCTCCCTGGC | 1877 |
| rs771977166 | in-del | -/TGGCCG | 1.83429e-05 | 0.00302838 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234440 | CCCCATCCTGCTCCC[-/TGGCCG]TGGCCCAGGTGCACC | 1877 |
| rs772058564 | snp | A/G | 1.87334e-05 | 0.00306045 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232511 | GCAAGGACCACGAGT[A/G]CAAGCTCTGTGGGGC | 1877 |
| rs772104258 | snp | C/T | 7.07376e-05 | 0.00594675 | intron-variant | E4F1 | GRCh38.p7 | 16:2232592 | GTGAGCTGGCCGCAC[C/T]TCGGGCTGGAGCCCG | 1877 |
| rs772106584 | snp | C/G | 1.69349e-05 | 0.00290984 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228467 | AAGGCCTGCCAGCGG[C/G]CCCCTCCGGAGGCCC | 1877 |
| rs772146423 | snp | C/T | 4.08973e-05 | 0.00452183 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233610 | TGGCAGTGGCAGCCC[C/T]GCAGCTGCCGGTACT | 1877 |
| rs772194830 | snp | A/G | 0.000168839 | 0.00918646 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228391 | GGACGATGTGCACAG[A/G]TGCGGCCGCTGCCAG | 1877 |
| rs772216765 | in-del | -/TCTGGACAGGGGCAGGT | 1.75185e-05 | 0.00295955 | intron-variant | E4F1 | GRCh38.p7 | 16:2232123 | GCAGTCTCTGGGGTC[-/TCTGGACAGGGGCAGGT]CCTGGGGCTTAGGCC | 1877 |
| rs772329286 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231285 | GCGGAAAAAGTTCGC[A/G]TCTCCTCTGGCCTCG | 1877 |
| rs772385410 | snp | A/C | 3.4623e-05 | 0.00416057 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233524 | GAACTCCGGCATCGT[A/C]CTTGAGCGCGCTGCT | 1877 |
| rs772406565 | snp | C/T | 2.47167e-05 | 0.00351536 | utr-variant-5-prime, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223586 | GACATGGTCGTAAAT[C/T]CGCCATCTTCCTGCG | 1877 |
| rs772419867 | snp | C/T | 3.31906e-05 | 0.0040736 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229590 | GCCGGCAGCACCAGG[C/T]CCAGAGGAGCCCATC | 1877 |
| rs772502120 | snp | C/T | 1.65954e-05 | 0.00288053 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229646 | CGGCCTCTCTGGCAG[C/T]AGACATCAGCCACGC | 1877 |
| rs772548010 | snp | A/G | 0.000125321 | 0.00791485 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234822 | GGAGGGGAGGGGGCC[A/G]GGGCTTGCCTAGCCC | 1877 |
| rs772565833 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227246 | ATGGAGTCTCTCTCT[A/G]TTGCCCCGGCTGGAG | 1877 |
| rs772602738 | snp | C/T | 5.55247e-05 | 0.00526871 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235566 | GGTGCAGACGGTCAT[C/T]GTCTAGCATGAGGTC | 1877 |
| rs772665318 | snp | A/C | 1.67455e-05 | 0.00289352 | intron-variant | E4F1 | GRCh38.p7 | 16:2232945 | GCCTGGTCCTGGGGG[A/C]TGGCTGTGGACGCAG | 1877 |
| rs772750611 | snp | A/C/G | 5.05534e-05 | 0.00502738 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234255 | AGGAGGTGCACGTGC[A/C/G]TGAGCGCCGCTTCCG | 1877 |
| rs772755097 | snp | A/G | 1.66258e-05 | 0.00288316 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232891 | ACGTGGTTGTCAGCA[A/G]AGAGGACGCACGTGC | 1877 |
| rs772830810 | snp | C/G | 1.66145e-05 | 0.00288218 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229664 | ACATCAGCCACGCAT[C/G]TGACCTTGTTGGTAA | 1877 |
| rs772894380 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235806 | TTTGCCCAGGCCCCC[A/G]CAGCAGCACCTGCCT | 1877 |
| rs772909148 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2233656 | GGAGACAGTAGGTGC[C/T]AGCACCACCTGCGGG | 1877 |
| rs772927222 | snp | C/T | 4.9755e-05 | 0.00498748 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229608 | AGAGGAGCCCATCAC[C/T]GTGGCCCACATCGTG | 1877 |
| rs772958777 | snp | C/G | 0.000182365 | 0.00954722 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223845 | GAGGCCCGGATGGCC[C/G]GAGCTGCGGGCTCGA | 1877 |
| rs773016452 | snp | A/G | 1.83849e-05 | 0.00303185 | intron-variant | E4F1 | GRCh38.p7 | 16:2234159 | TTGGCCTGATGCTGT[A/G]TGTGGCTGCAGGGCC | 1877 |
| rs773039495 | snp | A/G | 3.50355e-05 | 0.00418527 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235252 | GTGGTGCAGCAGATC[A/G]TGCACCAGGCTAGCG | 1877 |
| rs773050360 | snp | C/T | 1.83112e-05 | 0.00302576 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232346 | TGTGTGTGCGCTGTG[C/T]CACAAGACCTTCAAG | 1877 |
| rs773357685 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2236201 | AACACAGCCGCACCG[C/G]GATGTGGCTGACCGT | 1877 |
| rs773429419 | snp | C/T | 1.67587e-05 | 0.00289466 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232764 | TCTGCAGATGAGCGC[C/T]CCTACAAGTGCTCCA | 1877 |
| rs773481655 | snp | A/G | 3.54472e-05 | 0.00420979 | intron-variant | E4F1 | GRCh38.p7 | 16:2233192 | CCCAGAGGTGGGGGC[A/G]ACGGGGGGCCCCGGA | 1877 |
| rs773481721 | snp | C/G | 5.04299e-05 | 0.0050212 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234669 | CTTCCGAGAGAAGGG[C/G]TCACTGGTGCGGCAC | 1877 |
| rs773486881 | snp | A/C/T | 8.76393e-05 | 0.00661914 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235524 | TGCAGGCGAGCTGGT[A/C/T]ATCGCCTCGCCGGAG | 1877 |
| rs773540444 | snp | A/C | 0.000386392 | 0.0138941 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228491 | GAGGCCCTGCCTGCC[A/C]CCCCTGCCACCACAG | 1877 |
| rs773569538 | snp | A/T | 5.51253e-05 | 0.00524972 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234583 | CAGGTGTCTCCACAG[A/T]ACGCACAGCAGGTGC | 1877 |
| rs773636890 | snp | A/C/T | 3.54134e-05 | 0.00420781 | intron-variant | E4F1 | GRCh38.p7 | 16:2232614 | TGGAGCCCGGTAGCA[A/C/T]CCCGATGGTTGGCCC | 1877 |
| rs773661970 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227394 | TTGTTTTTTTTGAAA[C/T]GGAGTCTCGCTCTTT | 1877 |
| rs773662569 | snp | A/G | 1.72095e-05 | 0.00293333 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235390 | ACAGAGCAGGTGGCC[A/G]TGACGCTGGCCTCGG | 1877 |
| rs773673120 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226428 | GCACCTTAGAGCTTG[A/G]TTTGTGACTGGGAGC | 1877 |
| rs773690749 | snp | A/C | 1.72044e-05 | 0.0029329 | intron-variant | E4F1 | GRCh38.p7 | 16:2233833 | TGTTCTTGGTACTGC[A/C]AGGGCACAGCCTGCC | 1877 |
| rs773780534 | snp | G/T | 6.30577e-05 | 0.0056147 | intron-variant, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234954 | CCGCACACAGTGTTG[G/T]TGGAGTTCTCGTCCG | 1877 |
| rs773785440 | snp | G/T | 4.26958e-05 | 0.00462018 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233907 | GCGAGGCCTCAGCGG[G/T]GCCCAGGACCCACCC | 1877 |
| rs773805400 | snp | C/T | 1.70534e-05 | 0.00292 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232196 | CATCAAAGAGGTCAT[C/T]GTGGCTGCTGAGGCG | 1877 |
| rs773807971 | snp | C/T | 0.000167259 | 0.00914339 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223741 | CCCCCAGCGGCTTCC[C/T]CGGCCTCCCGGCGCC | 1877 |
| rs774016516 | snp | G/T | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233056 | CAGCCACATCATCGG[G/T]GACAGGCGAGCCTAT | 1877 |
| rs774070758 | snp | A/T | 1.66313e-05 | 0.00288364 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229671 | CCACGCATCTGACCT[A/T]GTTGGTAAGCCGACT | 1877 |
| rs774078037 | snp | G/T | 2.14987e-05 | 0.00327855 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223615 | CGGCGCGTTGCGACA[G/T]GGAGGGCGCGATGGC | 1877 |
| rs774101060 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231769 | GCCCCGGACGCACAT[C/T]CTCCCTATGTTGGTG | 1877 |
| rs774104454 | snp | A/G | 1.67618e-05 | 0.00289493 | intron-variant | E4F1 | GRCh38.p7 | 16:2232963 | GCTGTGGACGCAGCC[A/G]CCACTGGGGTGTGTG | 1877 |
| rs774106146 | snp | A/G | 1.67427e-05 | 0.00289328 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234315 | CCATTGCCCATGTGC[A/G]TGGCCACCGGCGCGT | 1877 |
| rs774169269 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222849 | ATCACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 1877 |
| rs774192186 | snp | C/G/T | 3.36634e-05 | 0.00410253 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234263 | CACGTGCGTGAGCGC[C/G/T]GCTTCCGCTGTGGCG | 1877 |
| rs774460791 | snp | A/G | 3.20005e-05 | 0.0039999 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228315 | GAAAAGCCAGACGGA[A/G]CCCTGGCTGCCCAGC | 1877 |
| rs774544014 | snp | C/T | 5.94972e-05 | 0.00545391 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234684 | CTCACTGGTGCGGCA[C/T]GTGCGACACCACACA | 1877 |
| rs774558148 | snp | C/T | 3.36005e-05 | 0.00409867 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233521 | GCAGAACTCCGGCAT[C/T]GTCCTTGAGCGCGCT | 1877 |
| rs774566483 | snp | A/G | 1.66037e-05 | 0.00288125 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229582 | CAGGTGGTGCCGGCA[A/G]CACCAGGCCCAGAGG | 1877 |
| rs774596350 | in-del | -/CT | 3.336e-05 | 0.00408398 | intron-variant | E4F1 | GRCh38.p7 | 16:2229547 | ATACAGACGACTCCC[-/CT]GTTTTCTTCCCCCTT | 1877 |
| rs774597354 | snp | C/T | 3.53294e-05 | 0.00420279 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235161 | GAGGGGTAGGGCAGG[C/T]GGGGGCGGGGAGGCT | 1877 |
| rs774636656 | snp | C/G | 1.94501e-05 | 0.00311844 | splice-donor-variant | E4F1 | GRCh38.p7 | 16:2232365 | AAGACCTTCAAGACG[C/G]TGAGCCGGCGTGCGG | 1877 |
| rs774834366 | snp | A/G | 3.54327e-05 | 0.00420893 | intron-variant | E4F1 | GRCh38.p7 | 16:2232618 | GCCCGGTAGCACCCC[A/G]ATGGTTGGCCCTGGG | 1877 |
| rs774852509 | snp | C/T | 2.00564e-05 | 0.00316667 | intron-variant | E4F1 | GRCh38.p7 | 16:2228564 | CCCTCCCGGGTTCAC[C/T]TGACAGGTGGGGGAG | 1877 |
| rs774862116 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230604 | CCTGGCCTTGGGCAG[C/T]CCTGGGGACTGGCTG | 1877 |
| rs774893538 | snp | C/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222659 | TGAGGCTAGGAGTTT[C/G]AGACCAGCCTAGTCT | 1877 |
| rs774940716 | snp | C/T | 5.02651e-05 | 0.00501299 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223753 | TCCTCGGCCTCCCGG[C/T]GCCCTTCAGCGAGGA | 1877 |
| rs775005572 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2223998 | TCTGGTGTGCGTCCA[C/G]AAGTGCTCGCGGGTT | 1877 |
| rs775051878 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224169 | TGGTTCCAAGAGGGT[C/G]GGGCCTCGGTTTCTC | 1877 |
| rs775079845 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2231509 | CAGTGGCTTCACAGC[C/T]GTTTCCCACTTGTCA | 1877 |
| rs775109020 | snp | G/T | 1.67691e-05 | 0.00289556 | intron-variant | E4F1 | GRCh38.p7 | 16:2234002 | ACCGGTAGGTGATGG[G/T]TGGGTGTGTGGCCCA | 1877 |
| rs775154393 | snp | C/T | 1.68125e-05 | 0.00289931 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232250 | CGAGGCCCCGGGCAG[C/T]CCCCGCCAGCAGGGG | 1877 |
| rs775170233 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235842 | GCCACTCCTAGACTC[A/G]CGTGCCTGGCCGCCC | 1877 |
| rs775238624 | snp | G/T | 2.20194e-05 | 0.00331801 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223662 | GCTCATACGGCAGAA[G/T]CCCAGGCCGAAGCCG | 1877 |
| rs775303227 | snp | A/G | 1.67469e-05 | 0.00289364 | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234327 | TGCGTGGCCACCGGC[A/G]CGTCCACTCAGACGA | 1877 |
| rs775330857 | snp | C/T | 1.66335e-05 | 0.00288383 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233067 | TCGGTGACAGGCGAG[C/T]CTATAGAGACTTCAC | 1877 |
| rs775396942 | snp | C/T | 1.7263e-05 | 0.00293789 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235361 | CCATCACCATCGCCA[C/T]CCCCGAGAGCCTGAC | 1877 |
| rs775597254 | snp | C/T | 2.07501e-05 | 0.00322097 | intron-variant | E4F1 | GRCh38.p7 | 16:2232430 | TCCCCCAGGAGGGCC[C/T]TGAGCTGCCACGCCC | 1877 |
| rs775633570 | in-del | -/ACGTGT | 3.94563e-05 | 0.00444146 | cds-indel, intron-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234629 | TGGAGGAGAAGCCGC[-/ACGTGT]GCCAGTTCTGCAGCC | 1877 |
| rs775691751 | snp | C/T | 0.000101232 | 0.00711376 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228394 | CGATGTGCACAGATG[C/T]GGCCGCTGCCAGGCA | 1877 |
| rs775692803 | snp | A/G | 3.4856e-05 | 0.00417454 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235317 | GGACGAGGAGACGGC[A/G]CTGGGCCCAGAGGCG | 1877 |
| rs775702309 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225718 | CTCAGGTGATCTGCC[C/T]GCCTCAGCCTCCCAA | 1877 |
| rs775705539 | snp | C/T | 2.42116e-05 | 0.00347926 | utr-variant-5-prime, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223590 | TGGTCGTAAATCCGC[C/T]ATCTTCCTGCGGCGC | 1877 |
| rs775707051 | snp | C/T | 3.74146e-05 | 0.00432503 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232512 | CAAGGACCACGAGTG[C/T]AAGCTCTGTGGGGCC | 1877 |
| rs775743732 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228658 | CAGGCACCTGGCTGC[A/G]GTGTGGGAGGGTCCG | 1877 |
| rs775793277 | snp | A/G | 0.00172087 | 0.0292827 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233611 | GGCAGTGGCAGCCCC[A/G]CAGCTGCCGGTACTG | 1877 |
| rs775801740 | in-del | -/AG | 1.75127e-05 | 0.00295906 | intron-variant | E4F1 | GRCh38.p7 | 16:2232130 | CTGGGGTCTCTGGAC[-/AG]GGGCAGGTCCTGGGG | 1877 |
| rs775892624 | snp | C/G | 0.000155994 | 0.00883021 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234797 | GTCTGGGCCGGTGGA[C/G]GTGGGAGGGGGAGGG | 1877 |
| rs775982429 | snp | A/G | 6.00763e-05 | 0.00548038 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234687 | ACTGGTGCGGCACGT[A/G]CGACACCACACAGGC | 1877 |
| rs776061277 | snp | C/G/T | 3.71135e-05 | 0.00430762 | intron-variant | E4F1 | GRCh38.p7 | 16:2234155 | GGGCTTGGCCTGATG[C/G/T]TGTGTGTGGCTGCAG | 1877 |
| rs776074345 | snp | C/T | 1.66065e-05 | 0.00288149 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229656 | GGCAGCAGACATCAG[C/T]CACGCATCTGACCTT | 1877 |
| rs776149285 | snp | A/G | 1.75625e-05 | 0.00296327 | stop-lost, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235234 | GACAGCCACATCATG[A/G]AGGTGGTGCAGCAGA | 1877 |
| rs776150915 | snp | A/G | 5.74135e-05 | 0.00535756 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234680 | AGGGCTCACTGGTGC[A/G]GCACGTGCGACACCA | 1877 |
| rs776165877 | snp | C/G | 1.65924e-05 | 0.00288027 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229592 | CGGCAGCACCAGGCC[C/G]AGAGGAGCCCATCAC | 1877 |
| rs776250184 | snp | C/G | 1.6628e-05 | 0.00288335 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232893 | GTGGTTGTCAGCAAA[C/G]AGGACGCACGTGCAG | 1877 |
| rs776300409 | snp | A/G | 0.000177132 | 0.00940929 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223837 | GGCTGGCAGAGGCCC[A/G]GATGGCCCGAGCTGC | 1877 |
| rs776338481 | snp | C/T | 1.66239e-05 | 0.00288299 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232804 | AGAGCTTCCGGGAGT[C/T]GGGTGCACTGACCCG | 1877 |
| rs776357419 | snp | C/G | 1.68032e-05 | 0.0028985 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232257 | CCGGGCAGCCCCCGC[C/G]AGCAGGGGCTGGGGC | 1877 |
| rs776389027 | snp | A/G | 7.25295e-05 | 0.00602158 | intron-variant, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223777 | GCGAGGAAGGTAACC[A/G]GGCCGACCCGGAGGG | 1877 |
| rs776413235 | snp | A/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222448 | TTGAACCCAGGAGGC[A/G]GAGGCTGCAGTGAGA | 1877 |
| rs776427017 | snp | C/G | 1.70261e-05 | 0.00291766 | intron-variant | E4F1 | GRCh38.p7 | 16:2234030 | CCATGGCAGTGGATG[C/G]GCTATAGGTGGCCGG | 1877 |
| rs776449987 | snp | A/G | 1.7654e-05 | 0.00297097 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235159 | GTGAGGGGTAGGGCA[A/G]GCGGGGGCGGGGAGG | 1877 |
| rs776466711 | snp | C/T | 1.77675e-05 | 0.00298051 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232331 | CAAGGATGGCCGCTA[C/T]GTGTGTGCGCTGTGC | 1877 |
| rs776564209 | snp | C/G | | | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232554 | CAAGGGCTCACTCAT[C/G]CGGCACCACCGGCGG | 1877 |
| rs776744880 | snp | A/G | 1.68247e-05 | 0.00290035 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228399 | TGCACAGATGCGGCC[A/G]CTGCCAGGCAGAGTT | 1877 |
| rs776770213 | snp | G/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230028 | CCGTAGGCAGCAACA[G/T]CCACCAGGCACCCAC | 1877 |
| rs776811146 | snp | A/G | 6.59957e-05 | 0.005744 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234566 | GGCCAGGCTGGCACT[A/G]ACAGGTGTCTCCACA | 1877 |
| rs776848740 | snp | A/G | 5.10452e-05 | 0.00505173 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228475 | CCAGCGGGCCCCTCC[A/G]GAGGCCCTGCCTGCC | 1877 |
| rs776896563 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2226189 | TGTCCCCATAGGATT[C/T]ATAGTCTCTGCCTTT | 1877 |
| rs776985376 | snp | A/G | 6.89881e-05 | 0.00587276 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235366 | ACCATCGCCACCCCC[A/G]AGAGCCTGACAGAGC | 1877 |
| rs777053167 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224010 | CCACAAGTGCTCGCG[A/G]GTTGCTGAGCCCCCG | 1877 |
| rs777128001 | snp | A/C | 3.48365e-05 | 0.00417337 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234409 | TCTCTGGCCGCAGGA[A/C]CCTGGCGCCTGATCC | 1877 |
| rs777200166 | snp | C/T | 1.66935e-05 | 0.00288903 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234940 | TCCTCACGGAAGACC[C/T]GCACACAGTGTTGGT | 1877 |
| rs777218258 | snp | A/C/G | 4.31884e-05 | 0.00464679 | missense, stop-gained, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223654 | TGACGGCCGCTCATA[A/C/G]GGCAGAAGCCCAGGC | 1877 |
| rs777310936 | snp | A/C | 1.66952e-05 | 0.00288917 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233041 | CTGCCGGCTTGGGGA[A/C]AGCCACATCATCGGT | 1877 |
| rs777312272 | snp | A/C | 2.24389e-05 | 0.00334947 | utr-variant-5-prime, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223605 | CATCTTCCTGCGGCG[A/C]GTTGCGACATGGAGG | 1877 |
| rs777314426 | in-del | -/C | 1.97443e-05 | 0.00314194 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235022 | TGTGGGGCCCTGGGG[-/C]CGTGCTGGGACCCAG | 1877 |
| rs777376815 | snp | A/C | | | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234505 | TGACCCAGCCCCTCC[A/C]TTGGGCCACAGGCGG | 1877 |
| rs777498644 | snp | G/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222273 | TTGTAATCCCAGCAC[G/T]TTGGGAGGCCGAGGC | 1877 |
| rs777606676 | snp | C/T | 1.76771e-05 | 0.00297291 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232572 | GCACCACCGGCGGCA[C/T]ACGGGTGAGCTGGCC | 1877 |
| rs777693154 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223533 | CCCTCCTCTTGCCGT[A/T]CCCTCACGCTGGCCT | 1877 |
| rs777736055 | snp | A/T | 2.56131e-05 | 0.00357853 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223564 | CGGCGCGGCCCGTTG[A/T]TATGACGACATGGTC | 1877 |
| rs777775176 | snp | A/C | 3.83237e-05 | 0.00437726 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235600 | GGGGTCCTGGCCGGG[A/C]AGGGACAGGGCAGAG | 1877 |
| rs777792153 | snp | C/T | 0.000217108 | 0.0104167 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234920 | CCCCGCGGCAGCCAC[C/T]ACCGTCCTCACGGAA | 1877 |
| rs777878673 | snp | C/T | 2.58702e-05 | 0.00359645 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233503 | CCTGCTGCACCAGGC[C/T]ATGCAGAACTCCGGC | 1877 |
| rs777972326 | snp | A/C | 1.98045e-05 | 0.00314672 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234757 | GCCGAGCACGGCACG[A/C]TGAACCGGCACCTGC | 1877 |
| rs778091081 | snp | A/C | 2.06345e-05 | 0.00321198 | intron-variant, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223811 | GGCCGGGGTGCGGGC[A/C]GTTCATCCCGGGCTG | 1877 |
| rs778183040 | snp | C/G/T | 5.15179e-05 | 0.00507511 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232305 | CAGGCCCAGGTGAAG[C/G/T]TACTGGTGAACAAGG | 1877 |
| rs778196055 | snp | G/T | 1.71023e-05 | 0.00292419 | intron-variant | E4F1 | GRCh38.p7 | 16:2228244 | TGTTCTCAGCAGCCT[G/T]GGGAAGTAGCTCTGC | 1877 |
| rs778322656 | snp | C/T | 1.82367e-05 | 0.00301961 | intron-variant | E4F1 | GRCh38.p7 | 16:2228537 | AGGTGAGCCCTCACC[C/T]ACTCCCCCATCCCCT | 1877 |
| rs778349498 | snp | A/G | 1.77354e-05 | 0.00297781 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235190 | CTCCCTGGCACAGCC[A/G]CTCTTGCTGAGCCGT | 1877 |
| rs778439444 | snp | C/T | 1.7306e-05 | 0.00294155 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235122 | TGAGGCCACGGAGAT[C/T]ATCGAGGGCACCCAG | 1877 |
| rs778472592 | snp | A/C/T | 0.000184164 | 0.00959416 | missense, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233135 | CATCCACGAAGTCCA[A/C/T]GTCCAGATGCAGGAG | 1877 |
| rs778521283 | snp | C/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2227001 | GGCCACTCACATGCT[C/G]CAGGGCACGCTCAAA | 1877 |
| rs778544963 | snp | A/G | 5.17005e-05 | 0.00508405 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235414 | GCCTCGGCCATCAGC[A/G]AGGGCACTGTGCTTG | 1877 |
| rs778558798 | snp | A/G | 5.27412e-05 | 0.00513496 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234416 | CCGCAGGACCCTGGC[A/G]CCTGATCCCCCCATC | 1877 |
| rs778698122 | snp | A/C | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2222138 | GAGGCAGGAGAATCG[A/C]TTGAACCTGGGAGGC | 1877 |
| rs778846111 | snp | C/T | 3.38908e-05 | 0.00411634 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228464 | CAGAAGGCCTGCCAG[C/T]GGGCCCCTCCGGAGG | 1877 |
| rs778872254 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225542 | GCAATGGTGCGATCT[C/T]GGCTCACCGCAACCT | 1877 |
| rs778927200 | snp | G/T | 1.69046e-05 | 0.00290723 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234928 | CAGCCACCACCGTCC[G/T]CACGGAAGACCCGCA | 1877 |
| rs778936219 | snp | A/G/T | 7.08032e-05 | 0.00594956 | intron-variant | E4F1 | GRCh38.p7 | 16:2232588 | ACGGGTGAGCTGGCC[A/G/T]CACCTCGGGCTGGAG | 1877 |
| rs778942051 | snp | C/T | 6.99423e-05 | 0.00591323 | intron-variant | E4F1 | GRCh38.p7 | 16:2233879 | CTTCCTGTGGTTCCC[C/T]AGCAGGTGGCCAGCG | 1877 |
| rs778945403 | snp | C/G | 5.02525e-05 | 0.00501236 | intron-variant | E4F1 | GRCh38.p7 | 16:2229698 | GACTTCCATGAATCG[C/G]TGGCCTGATAGACCT | 1877 |
| rs778961089 | snp | G/T | 4.24881e-05 | 0.00460893 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223634 | GGGCGCGATGGCAGT[G/T]CGGGTGACGGCCGCT | 1877 |
| rs779024155 | snp | A/G | 1.88152e-05 | 0.00306712 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232507 | AGCCGCAAGGACCAC[A/G]AGTGCAAGCTCTGTG | 1877 |
| rs779031665 | snp | A/C | 3.04586e-05 | 0.00390235 | intron-variant, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234984 | GTGGTAGCTGACACC[A/C]AGGAGTATATCATCG | 1877 |
| rs779059622 | in-del | -/TCCCCCCATCCTGC | 1.76799e-05 | 0.00297315 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234421 | GACCCTGGCGCCTGA[-/TCCCCCCATCCTGC]TCCCCCCATCCTGCT | 1877 |
| rs779227164 | snp | C/T | 3.31802e-05 | 0.00407296 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229638 | GGTGGAGGCGGCCTC[C/T]CTGGCAGCAGACATC | 1877 |
| rs779237742 | snp | A/G | | | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235006 | ATATCATCGAGGTGG[A/G]TGTGGGGCCCTGGGG | 1877 |
| rs779313063 | snp | C/T | 5.00931e-05 | 0.0050044 | intron-variant | E4F1 | GRCh38.p7 | 16:2232937 | GGGCAGCTGCCTGGT[C/T]CTGGGGGCTGGCTGT | 1877 |
| rs779330042 | snp | C/G | 6.36234e-05 | 0.00563983 | intron-variant | E4F1 | GRCh38.p7 | 16:2228288 | CTGGGGGAATCTGTT[C/G]TAGGGCTGGAGGAAA | 1877 |
| rs779485187 | snp | A/G | 1.71434e-05 | 0.0029277 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234200 | GCCTGCGCGCAGTGT[A/G]GCAAGGCCTTCCCCA | 1877 |
| rs779527527 | snp | A/G | 2.01209e-05 | 0.00317176 | intron-variant | E4F1 | GRCh38.p7 | 16:2232379 | GGTGAGCCGGCGTGC[A/G]GGGAGCCAGTGTGTG | 1877 |
| rs779587359 | snp | C/G | 3.79831e-05 | 0.00435776 | intron-variant | E4F1 | GRCh38.p7 | 16:2234146 | GCGGGTGATGGGCTT[C/G]GCCTGATGCTGTGTG | 1877 |
| rs779587447 | snp | C/T | 0.000104588 | 0.0072307 | utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235284 | CGGCCACCAGATCAT[C/T]GTGCAGAACGTCACC | 1877 |
| rs779615574 | snp | A/G | 1.74391e-05 | 0.00295283 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232318 | AGCTACTGGTGAACA[A/G]GGATGGCCGCTATGT | 1877 |
| rs779637404 | snp | A/G | | | intron-variant | E4F1 | GRCh38.p7 | 16:2224846 | GTTGGATTGGATCTC[A/G]GCACTGTGAAGGCCT | 1877 |
| rs779688502 | snp | A/G | 4.87294e-05 | 0.00493582 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233481 | CCAGCGAGGGCAGCC[A/G]TGAGAACCTGCTGCA | 1877 |
| rs779963235 | in-del | -/CGGTCATCGT | 1.6593e-05 | 0.00288031 | utr-variant-3-prime, frameshift-variant, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235559 | AGCTGGAGGTGCAGA[-/CGGTCATCGT]CTAGCATGAGGTCTG | 1877 |
| rs779968333 | snp | C/T | 1.80794e-05 | 0.00300656 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234435 | GATCCCCCCATCCTG[C/T]TCCCTGGCCGTGGCC | 1877 |
| rs779974964 | snp | C/T | 7.07977e-05 | 0.00594927 | intron-variant | E4F1 | GRCh38.p7 | 16:2232594 | GAGCTGGCCGCACCT[C/T]GGGCTGGAGCCCGGT | 1877 |
| rs779986954 | snp | A/G | 1.78832e-05 | 0.00299019 | intron-variant | E4F1 | GRCh38.p7 | 16:2228528 | TGGGCCAGGAGGTGA[A/G]CCCTCACCCACTCCC | 1877 |
| rs780070482 | snp | G/T | 1.69017e-05 | 0.00290699 | intron-variant | E4F1 | GRCh38.p7 | 16:2232727 | CAGCCTGCTGGGGCT[G/T]CCCGGGGCTGACTAG | 1877 |
| rs780085308 | snp | G/T | 4.20743e-05 | 0.00458643 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233964 | CGACAGCAGCCACCC[G/T]GGAGGCCCACAAGAG | 1877 |
| rs780095985 | snp | C/G | 2.07915e-05 | 0.00322418 | intron-variant | E4F1 | GRCh38.p7 | 16:2232406 | TGTGGGTGGCAGGCC[C/G]CCTCCTGTTCCCCCA | 1877 |
| rs780172664 | snp | C/T | 3.38662e-05 | 0.00411484 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2228469 | GGCCTGCCAGCGGGC[C/T]CCTCCGGAGGCCCTG | 1877 |
| rs780354367 | snp | A/C/G | 0.00038162 | 0.0138089 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234932 | CACCACCGTCCTCAC[A/C/G]GAAGACCCGCACACA | 1877 |
| rs780367917 | snp | A/C/G | 8.50094e-05 | 0.00651909 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223643 | GGCAGTGCGGGTGAC[A/C/G]GCCGCTCATACGGCA | 1877 |
| rs780537089 | snp | A/C | 1.76092e-05 | 0.0029672 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235337 | GCCCAGAGGCGGCTG[A/C]CGCCGACACCATCAC | 1877 |
| rs780555103 | snp | A/G | 1.69516e-05 | 0.00291127 | intron-variant | E4F1 | GRCh38.p7 | 16:2229716 | GCCTGATAGACCTTC[A/G]TGGTTGGGGCCAGAG | 1877 |
| rs780638902 | snp | C/T | 1.67133e-05 | 0.00289074 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233034 | GCTGGAGCTGCCGGC[C/T]TGGGGACAGCCACAT | 1877 |
| rs780679293 | snp | A/G | 1.77432e-05 | 0.00297847 | intron-variant, missense | E4F1 | GRCh38.p7 | 16:2228356 | CCAGGCCCTGCTGAC[A/G]GCAGGCTCGTTGCAG | 1877 |
| rs780721615 | snp | C/T | 0.00010124 | 0.00711406 | synonymous-codon, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2234250 | GCACCAGGAGGTGCA[C/T]GTGCGTGAGCGCCGC | 1877 |
| rs780726805 | snp | A/G | 1.68052e-05 | 0.00289867 | intron-variant | E4F1 | GRCh38.p7 | 16:2232951 | TCCTGGGGGCTGGCT[A/G]TGGACGCAGCCGCCA | 1877 |
| rs780743461 | snp | A/G | 2.05345e-05 | 0.00320419 | intron-variant | E4F1 | GRCh38.p7 | 16:2232398 | AGCCAGTGTGTGGGT[A/G]GCAGGCCCCCTCCTG | 1877 |
| rs780767311 | snp | C/T | 4.06446e-05 | 0.00450784 | intron-variant, synonymous-codon | E4F1 | GRCh38.p7 | 16:2228307 | GGCTGGAGGAAAAGC[C/T]AGACGGAGCCCTGGC | 1877 |
| rs780776291 | snp | A/G | 1.66643e-05 | 0.0028865 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235579 | ATCGTCTAGCATGAG[A/G]TCTGCGGGGTCCTGG | 1877 |
| rs780779672 | snp | C/G | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221822 | AATTAGCTAGTGATG[C/G]GCACCTGTAGTCCCA | 1877 |
| rs780809457 | snp | C/T | 1.74199e-05 | 0.00295121 | utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235286 | GCCACCAGATCATCG[C/T]GCAGAACGTCACCAT | 1877 |
| rs780844249 | snp | C/T | 2.01209e-05 | 0.00317176 | intron-variant | E4F1 | GRCh38.p7 | 16:2232453 | CCACGCCCTCCCCCA[C/T]AGGGCAGCATCCTCA | 1877 |
| rs780963484 | in-del | -/TCCGCCATCT | 2.47589e-05 | 0.00351836 | utr-variant-5-prime, frameshift-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223585 | CGACATGGTCGTAAA[-/TCCGCCATCT]TCCTGCGGCGCGTTG | 1877 |
| rs781105800 | snp | A/G | 4.33004e-05 | 0.00465277 | intron-variant | E4F1 | GRCh38.p7 | 16:2233411 | CCAGGCTGCCTGGCC[A/G]GCCTCCTCTCTCTGC | 1877 |
| rs781159338 | in-del | -/C | 2.93165e-05 | 0.0038285 | intron-variant | E4F1 | GRCh38.p7 | 16:2233674 | CACCACCTGCGGGCT[-/C]CTCCCAGGGCTGGAT | 1877 |
| rs781197252 | snp | C/T | 1.82227e-05 | 0.00301845 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2234744 | CGGCCGTGGCTTCGC[C/T]GAGCACGGCACGCTG | 1877 |
| rs781239839 | snp | A/G | 1.66045e-05 | 0.00288132 | missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232863 | GAGAAAATCCGCTTC[A/G]GTGTGAGCAAGGACG | 1877 |
| rs781291123 | snp | A/G | 3.37126e-05 | 0.0041055 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235588 | CATGAGGTCTGCGGG[A/G]TCCTGGCCGGGCAGG | 1877 |
| rs781412590 | snp | A/G | 1.66324e-05 | 0.00288374 | missense, intron-variant, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233975 | ACCCTGGAGGCCCAC[A/G]AGAGGGGCCACACCG | 1877 |
| rs781466456 | snp | C/T | 2.08162e-05 | 0.00322609 | intron-variant, upstream-variant-2KB | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235015 | AGGTGGGTGTGGGGC[C/T]CTGGGGCCGTGCTGG | 1877 |
| rs781566744 | snp | C/T | | | upstream-variant-2KB | E4F1 | GRCh38.p7 | 16:2221947 | AAATCTGGCCAGGCT[C/T]GGTGGCTCATGCCTG | 1877 |
| rs781584850 | snp | C/T | 3.33e-05 | 0.00408031 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2233120 | TGCCAAGGGCACCGT[C/T]ATCCACGAAGTCCAC | 1877 |
| rs781587768 | snp | C/T | 8.64461e-05 | 0.00657386 | missense, upstream-variant-2KB, nc-transcript-variant | E4F1, DNASE1L2 | GRCh38.p7 | 16:2235097 | CCACTGCGGACGATG[C/T]GGAGACCAGTGAGGC | 1877 |
| rs781610054 | snp | C/G | 0.000122182 | 0.00781512 | intron-variant, synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223805 | GGGTGCGGCCGGGGT[C/G]CGGGCAGTTCATCCC | 1877 |
| rs781685270 | snp | C/G | 0.000267463 | 0.0115611 | synonymous-codon, missense, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2223709 | GGGTGCAGTTGCGGC[C/G]GTGGCGGCGGCCTTG | 1877 |
| rs781712464 | snp | A/G | 4.97591e-05 | 0.00498769 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2229599 | ACCAGGCCCAGAGGA[A/G]CCCATCACTGTGGCC | 1877 |
| rs781739631 | snp | A/C | 1.68459e-05 | 0.00290219 | synonymous-codon, nc-transcript-variant | E4F1 | GRCh38.p7 | 16:2232241 | TGAGATGGCCGAGGC[A/C]CCGGGCAGCCCCCGC | 1877 |
| rs796342712 | snp | C/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2230790 | ATGCCACTCAGAGCT[C/T]GGAATGTTCATGTGG | 1877 |
| rs796554580 | snp | G/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2228179 | GGCCCCTGCAGACCT[G/T]CAGAGGATAGGGGCT | 1877 |
| rs796751941 | snp | A/T | | | intron-variant | E4F1 | GRCh38.p7 | 16:2225803 | TAGGAAAAAAAAAAA[A/T]AAAAAAAAAAGGCTG | 1877 |