SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3683 | snp | A/C | 0.0391999 | 0.1344 | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239048749 | GGCCGAGCTAAGAAC[A/C]CGCTCAGCTTCGTTA | 9759 |
rs169731 | snp | C/T | 0.454061 | 0.144427 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239230401 | aaaaaGCAAAGCAGG[C/T]GACATGTTCCGTGGC | 9759 |
rs172365 | snp | C/T | 0.476833 | 0.105105 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239230446 | TGGCCAATCCTTGCC[C/T]GTGGCTGGCAAGCTG | 9759 |
rs291329 | snp | C/T | 0.499759 | 0.0109798 | intron-variant | HDAC4 | GRCh38.p7 | 2:239222726 | CAATGCAAAAGCAAT[C/T]GAATAGAAACAATAA | 9759 |
rs291330 | snp | A/G | 0.49998 | 0.00319482 | intron-variant | HDAC4 | GRCh38.p7 | 2:239223207 | CCTAACAGCTGGGCC[A/G]AAGTAGGAACCACTA | 9759 |
rs291331 | snp | A/C | 0.163892 | 0.234703 | intron-variant | HDAC4 | GRCh38.p7 | 2:239223262 | ATTTAAAAATAGAAA[A/C]CATTGGAGAAGAAGA | 9759 |
rs291332 | snp | C/T | 0.130694 | 0.219696 | intron-variant | HDAC4 | GRCh38.p7 | 2:239223609 | TGAACACACGGTACG[C/T]AGCTGAGTGACAGAT | 9759 |
rs291333 | snp | G/T | 0.323197 | 0.239044 | intron-variant | HDAC4 | GRCh38.p7 | 2:239223680 | CATCATTGCTGTAAT[G/T]AGGAGCAACCACGAG | 9759 |
rs291334 | snp | A/G | 0.36955 | 0.219562 | intron-variant | HDAC4 | GRCh38.p7 | 2:239224582 | CCCCTCCACTCCCGA[A/G]CCCTGCTCTGCCTTC | 9759 |
rs291335 | snp | A/G | 0.499961 | 0.0043928 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239226151 | AGCCTTAAAGCACAC[A/G]AAGCTGGTAATAAAA | 9759 |
rs291336 | snp | A/G | 0.0614824 | 0.164198 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239226343 | CACTGAGTATCTCTC[A/G]GGGAGGATTCCACAG | 9759 |
rs291337 | snp | A/G | 0.499968 | 0.00399348 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239227891 | GCAGCTGGGAGACCT[A/G]GCAGAGGGCCCGGGC | 9759 |
rs291338 | snp | A/G | 0.131723 | 0.220251 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239228266 | GGAGGCCATGTGGCC[A/G]AAGGGAGACAGGAAG | 9759 |
rs291339 | snp | C/T | 0.4776 | 0.103433 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239230476 | GCCGAGTCCGTGGGC[C/T]GGAGGGCATTGATTC | 9759 |
rs484661 | snp | C/T | 0.168135 | 0.236216 | intron-variant | HDAC4 | GRCh38.p7 | 2:239201514 | CCTGTAATTACTATT[C/T]GCTGAGAGCCTACAG | 9759 |
rs486396 | snp | C/T | 0.233527 | 0.249457 | intron-variant | HDAC4 | GRCh38.p7 | 2:239201668 | GCCCCACCTCCCTTC[C/T]CAACAGCACCAGAAA | 9759 |
rs489806 | snp | A/C | 0.499879 | 0.0077866 | intron-variant | HDAC4 | GRCh38.p7 | 2:239177760 | TGAGAACATGACAGG[A/C]AGCCCACTAAAACGT | 9759 |
rs496316 | snp | A/G | 0.142272 | 0.225598 | intron-variant | HDAC4 | GRCh38.p7 | 2:239233535 | GCTTTGGGAAAGTCT[A/G]TACAGGTTGAGTATC | 9759 |
rs506324 | snp | C/T | 0.379746 | 0.213696 | intron-variant | HDAC4 | GRCh38.p7 | 2:239182650 | ATTTATAACAGATTA[C/T]CTGTAGAGCAAAGCC | 9759 |
rs507159 | snp | C/G | 0.499722 | 0.0117779 | intron-variant | HDAC4 | GRCh38.p7 | 2:239198786 | AATATATATTTTTAT[C/G]TTTCATGAGAAATTC | 9759 |
rs518274 | snp | A/G | 0.499977 | 0.00339449 | intron-variant | HDAC4 | GRCh38.p7 | 2:239209462 | acaaacacttatcct[A/G]ctattctacggggaa | 9759 |
rs519165 | snp | A/G | 0.366473 | 0.221211 | intron-variant | HDAC4 | GRCh38.p7 | 2:239219687 | AGGCTCAGATTAGAC[A/G]GGTAAAAAGCCCCAA | 9759 |
rs522916 | snp | C/G | 0.49998 | 0.00319482 | intron-variant | HDAC4 | GRCh38.p7 | 2:239209980 | GGGTGGAGAGGCAGG[C/G]AGCGGGGGCGTGGGA | 9759 |
rs528213 | snp | G/T | 0.499853 | 0.008585 | intron-variant | HDAC4 | GRCh38.p7 | 2:239205380 | ACGTTATCCAACAAA[G/T]GAAATGCAGTCACAG | 9759 |
rs530689 | snp | A/G | 0.499987 | 0.00259581 | intron-variant | HDAC4 | GRCh38.p7 | 2:239216970 | GGCGTGAATGCAGTC[A/G]CCTGTCTTTTGCTAC | 9759 |
rs531993 | snp | A/T | 0.492435 | 0.0610346 | intron-variant | HDAC4 | GRCh38.p7 | 2:239189781 | GCTGGAGTCACCGGG[A/T]GTTGAGGGTGCCGGA | 9759 |
rs541417 | snp | C/T | 0.492435 | 0.0610346 | intron-variant | HDAC4 | GRCh38.p7 | 2:239203043 | GCTGGCAGCGCTGAG[C/T]GGAGCCTCAGCCCTA | 9759 |
rs548717 | snp | G/T | 0.167158 | 0.235875 | intron-variant | HDAC4 | GRCh38.p7 | 2:239203849 | AATTATCAGCTTCAA[G/T]GGATTCGAGTAGGAC | 9759 |
rs549639 | snp | C/G | 0.499995 | 0.00159744 | intron-variant | HDAC4 | GRCh38.p7 | 2:239212043 | GAGCAAAGTCTTCAA[C/G]AGCATTTTTCACTTA | 9759 |
rs551326 | snp | C/T | 0.267091 | 0.249415 | intron-variant | HDAC4 | GRCh38.p7 | 2:239179915 | ACATCAACGTGCTTG[C/T]GCACCCAAGTGTGCG | 9759 |
rs552298 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239232003 | AGCCTCGATTGAGGA[C/G]AGGGGCGCTTCGGGG | 9759 |
rs552356 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239231982 | CGCTTCGGGGAGGAC[A/G]CCTACCTCAGGCATC | 9759 |
rs552954 | snp | A/G | 0.498611 | 0.0263212 | intron-variant | HDAC4 | GRCh38.p7 | 2:239173484 | accccgagcaaacaa[A/G]gaatggaagggaaac | 9759 |
rs554946 | snp | A/C | 0.499992 | 0.00199679 | intron-variant | HDAC4 | GRCh38.p7 | 2:239218088 | tttttgttttttgag[A/C]tggggcctcactctg | 9759 |
rs555834 | snp | C/T | 0.463559 | 0.129972 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239231427 | CTGGGACAGCGGCCA[C/T]GGGATCTGAGGCTCT | 9759 |
rs563856 | snp | C/T | 0.236144 | 0.249616 | intron-variant | HDAC4 | GRCh38.p7 | 2:239200386 | GGGGAGGGGCACGCA[C/T]GCAAAGTAGAGACGA | 9759 |
rs566435 | snp | G/T | 0.499918 | 0.00638925 | intron-variant | HDAC4 | GRCh38.p7 | 2:239200648 | AAGAAGAAGGTGCTT[G/T]GTATTGCTTTCCATT | 9759 |
rs574636 | snp | C/T | 0.176219 | 0.238865 | intron-variant | HDAC4 | GRCh38.p7 | 2:239221070 | GTGAGGCCTCTGTGC[C/T]TCACTCAGCGGGTCA | 9759 |
rs577090 | snp | A/G | 0.495252 | 0.0484902 | intron-variant | HDAC4 | GRCh38.p7 | 2:239187239 | CAATGGCCGACGGGG[A/G]CTTCTGAGAGGCACA | 9759 |
rs581362 | snp | A/G | 0.499977 | 0.00339449 | intron-variant | HDAC4 | GRCh38.p7 | 2:239210389 | TGGATTTGCTTTTCC[A/G]AGCTTTTAATAATCG | 9759 |
rs583445 | snp | C/G | 0.49925 | 0.0193545 | intron-variant | HDAC4 | GRCh38.p7 | 2:239199266 | AGGCAGCTTAGACTT[C/G]CCAGCAAGGCCTAAG | 9759 |
rs584293 | snp | A/C | 0.493703 | 0.0557558 | intron-variant | HDAC4 | GRCh38.p7 | 2:239199421 | agcaggaccatttct[A/C]taacgggaaggaatc | 9759 |
rs589712 | snp | A/G | 0.235564 | 0.249583 | intron-variant | HDAC4 | GRCh38.p7 | 2:239200756 | TGTGTGGGGCTGGGC[A/G]GGAGAGAGACGCGTC | 9759 |
rs592695 | snp | A/C | 0.265727 | 0.249505 | intron-variant | HDAC4 | GRCh38.p7 | 2:239180244 | GCACACACACCTTTC[A/C]AACCCCTAGGCTTCT | 9759 |
rs593337 | snp | A/G | 0.499996 | 0.00139776 | intron-variant | HDAC4 | GRCh38.p7 | 2:239205720 | GGGAGGACGAGGAGG[A/G]AGGGAGAAGAACAAA | 9759 |
rs598377 | snp | C/G | 0.159622 | 0.233092 | intron-variant | HDAC4 | GRCh38.p7 | 2:239200265 | AAGCTGACATTCAAA[C/G]GCCTGAACGGTCATA | 9759 |
rs604067 | snp | A/G | 0.447291 | 0.153545 | intron-variant | HDAC4 | GRCh38.p7 | 2:239201630 | GCTCAAGGCCGAGAC[A/G]ACAGCCCCAGAGGCA | 9759 |
rs604433 | snp | A/G | 0.168785 | 0.236441 | intron-variant | HDAC4 | GRCh38.p7 | 2:239220468 | GATCCGCAATCTGTC[A/G]GATTTCTTTCATCTT | 9759 |
rs604827 | snp | C/G | 0.165527 | 0.235296 | intron-variant | HDAC4 | GRCh38.p7 | 2:239220527 | ACTGTCTTCCCCTAC[C/G]AAGCACAAACTGTCC | 9759 |
rs605614 | snp | C/T | 0.499984 | 0.00279548 | intron-variant | HDAC4 | GRCh38.p7 | 2:239212747 | CCAGAGAGGACCCTC[C/T]CAGCTCCTCCCTGGA | 9759 |
rs606531 | snp | A/G | 0.166832 | 0.235761 | intron-variant | HDAC4 | GRCh38.p7 | 2:239220422 | CTTTTTCAGTGCACA[A/G]TGTATGCTTTAATTT | 9759 |
rs607835 | snp | C/T | 0.499998 | 0.000998401 | intron-variant | HDAC4 | GRCh38.p7 | 2:239213222 | GCCCCTCCCTGGCCC[C/T]TACTTTGCTGTTATG | 9759 |
rs608911 | snp | A/G | 0.267908 | 0.249358 | intron-variant | HDAC4 | GRCh38.p7 | 2:239181595 | AAGCAAGCTCTTGCC[A/G]TGTCCTTCATCAGGG | 9759 |
rs614200 | snp | C/T | 0.375 | 0.216506 | intron-variant | HDAC4 | GRCh38.p7 | 2:239184817 | GTCCCTCAGTGTCTG[C/T]CCTGGAGACTGTGTC | 9759 |
rs614588 | snp | C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239184860 | GTCCCTCAGTGTCTG[C/T]CCTGGAGGATGTATC | 9759 |
rs615994 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | HDAC4 | GRCh38.p7 | 2:239213956 | atgtgacctaggcag[A/G]tttctctacctccct | 9759 |
rs617829 | snp | A/G | 0.491783 | 0.0635686 | intron-variant | HDAC4 | GRCh38.p7 | 2:239221168 | ATTCGCAAGAACACT[A/G]ATACCATCTGACAGG | 9759 |
rs618655 | snp | A/G | 0.273318 | 0.24891 | intron-variant | HDAC4 | GRCh38.p7 | 2:239179190 | TGTGCTCCATGAGTG[A/G]CTGCGCTGGCACAGC | 9759 |
rs621578 | snp | C/T | 0.171704 | 0.237423 | intron-variant | HDAC4 | GRCh38.p7 | 2:239182089 | TCTGCCCTGGGGACC[C/T]GGAGCTGTGTACACA | 9759 |
rs625839 | snp | A/G | 0.444133 | 0.157519 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194472 | GTGTGCCTGTGAGGC[A/G]GGCAGGAGCGTCACC | 9759 |
rs631292 | snp | C/T | 0.197703 | 0.244469 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239195145 | CAGGAGGTGCCGTAG[C/T]GAGAACAGCGACAGC | 9759 |
rs637265 | snp | C/T | 0.499995 | 0.00159744 | intron-variant | HDAC4 | GRCh38.p7 | 2:239218124 | AAACAGAATATAAAA[C/T]TGGATGAAAATTTTA | 9759 |
rs640780 | snp | G/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239172425 | catttacatttaatg[G/T]aattattgatatatt | 9759 |
rs645357 | snp | C/G | 0.245346 | 0.249957 | intron-variant | HDAC4 | GRCh38.p7 | 2:239187170 | GTTGGCCTGCAGGAA[C/G]GCAGGGAAGCCGGAG | 9759 |
rs646326 | snp | C/T | 0.490007 | 0.0699769 | intron-variant | HDAC4 | GRCh38.p7 | 2:239187391 | AATGTGAGCCTATGG[C/T]GCAAAAACTAAATAA | 9759 |
rs653976 | snp | A/G | 0.444666 | 0.15686 | intron-variant | HDAC4 | GRCh38.p7 | 2:239192777 | TGTGTTTATCCCTGG[A/G]AAGCACGGGCCCGCT | 9759 |
rs669106 | snp | A/G | 0.48955 | 0.071525 | intron-variant | HDAC4 | GRCh38.p7 | 2:239184460 | GCTGTGCCCTATGAG[A/G]GGGGGTCCCTCAGTG | 9759 |
rs672183 | snp | C/T | 0.197082 | 0.244335 | intron-variant | HDAC4 | GRCh38.p7 | 2:239178567 | TTTCTTCTTTTTTGA[C/T]GAAACAAGATCTTGC | 9759 |
rs673912 | snp | A/G | 0.356169 | 0.226336 | intron-variant | HDAC4 | GRCh38.p7 | 2:239172340 | AAAACATACACTAAA[A/G]GCAAGACAAGTGCAT | 9759 |
rs674540 | snp | A/G | 0.197393 | 0.244402 | intron-variant | HDAC4 | GRCh38.p7 | 2:239189081 | GATATAGATAACTTA[A/G]TCTGGTTTTGTGGGA | 9759 |
rs675093 | snp | A/C | 0.499977 | 0.00339449 | intron-variant | HDAC4 | GRCh38.p7 | 2:239209937 | CAGACCCCTGGAGAC[A/C]CCACTTTACGCCCAC | 9759 |
rs675525 | snp | C/T | 0.198324 | 0.244601 | intron-variant | HDAC4 | GRCh38.p7 | 2:239198031 | ctaatttctctccct[C/T]cctcccttccttcca | 9759 |
rs678228 | snp | A/G | 0.499859 | 0.0083854 | intron-variant | HDAC4 | GRCh38.p7 | 2:239205328 | GCGAAACAGCAGACC[A/G]CTGAGACAGAGTTCA | 9759 |
rs680392 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | HDAC4 | GRCh38.p7 | 2:239217984 | gtggttccagctact[C/T]ggaaggctgaggcag | 9759 |
rs680564 | snp | A/G | 0.432944 | 0.170387 | intron-variant | HDAC4 | GRCh38.p7 | 2:239192672 | GCGGAAGAGGGAACC[A/G]CAACCTGACAGTCAT | 9759 |
rs681715 | snp | A/T | 0.388021 | 0.208447 | intron-variant | HDAC4 | GRCh38.p7 | 2:239182693 | GCCATCAGGACAAAC[A/T]GGATTTCAACACTCC | 9759 |
rs686606 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | HDAC4 | GRCh38.p7 | 2:239179399 | AGCTCAAGCTCCTGC[C/T]GGATCAGTGGTGGCA | 9759 |
rs687778 | snp | C/T | 0.418491 | 0.184691 | intron-variant | HDAC4 | GRCh38.p7 | 2:239205021 | ACCTTCCCCCGTCCC[C/T]GAGCCGCCTCTGTCC | 9759 |
rs688680 | snp | A/G | 0.141258 | 0.225111 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239232067 | CGTCCTCCCCGAAGC[A/G]CCCCTCTCCTCAATC | 9759 |
rs709271 | snp | C/T | 0.499866 | 0.0081858 | intron-variant | HDAC4 | GRCh38.p7 | 2:239219062 | agatccctgaggaat[C/T]gccacactgatttcc | 9759 |
rs709272 | snp | A/G | 0.499977 | 0.00339449 | intron-variant | HDAC4 | GRCh38.p7 | 2:239219169 | ccgcaataaacatac[A/G]tgtgcatgtgtcttt | 9759 |
rs747787 | snp | A/G | 0.498982 | 0.0225409 | intron-variant | HDAC4 | GRCh38.p7 | 2:239110623 | GAGAGTGAGAACCTC[A/G]CAGACTGCAGAACAC | 9759 |
rs753302 | snp | C/T | 0.310632 | 0.242536 | intron-variant | HDAC4 | GRCh38.p7 | 2:239192441 | AAAGTCTGAAGCAAA[C/T]GTAGGTGAACGCTGA | 9759 |
rs843461 | snp | A/G | 0.362941 | 0.223034 | intron-variant | HDAC4 | GRCh38.p7 | 2:239397395 | ACGAGCAGCTGTCAC[A/G]TGCTCCCGTAGCTGA | 9759 |
rs843462 | snp | A/G | 0.148326 | 0.228391 | intron-variant | HDAC4 | GRCh38.p7 | 2:239397060 | TGTTGACTGTTCTTG[A/G]CGCTGTTACAGGCGC | 9759 |
rs843463 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HDAC4 | GRCh38.p7 | 2:239396636 | CCTGTGTAAGCTTAA[C/T]AGTCAATATATAAAG | 9759 |
rs843469 | snp | A/G | 0.247905 | 0.249991 | intron-variant | HDAC4 | GRCh38.p7 | 2:239183921 | ACTAGGTTCCTTTCC[A/G]TGTTAGTTCCTCCCT | 9759 |
rs843470 | snp | C/T | 0.170084 | 0.236883 | intron-variant | HDAC4 | GRCh38.p7 | 2:239208060 | gggcgcggtggctca[C/T]gcctgtaatcccagc | 9759 |
rs860022 | snp | C/T | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239218456 | tccttacatcttata[C/T]aaaaattaattcaag | 9759 |
rs860023 | snp | C/G | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239219018 | acttttacactgttg[C/G]tgggactgtaaacta | 9759 |
rs860936 | snp | A/G | 0.472147 | 0.114677 | intron-variant | HDAC4 | GRCh38.p7 | 2:239396183 | TTCAAGACCAGCCTG[A/G]GCAACATAGTGAGAC | 9759 |
rs863617 | snp | C/T | 0.4444 | 0.15719 | intron-variant | HDAC4 | GRCh38.p7 | 2:239208283 | agtgagccgagatcg[C/T]gccactgcactccag | 9759 |
rs864012 | snp | A/G | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239218946 | cccagttagaatggc[A/G]atcattaaaaagtca | 9759 |
rs870790 | snp | A/G | 0.417034 | 0.18601 | intron-variant | HDAC4 | GRCh38.p7 | 2:239394311 | AATATGTTTGTGTAC[A/G]TAAACATTTTGGAGT | 9759 |
rs895802 | snp | A/T | 0.49928 | 0.018956 | intron-variant | HDAC4 | GRCh38.p7 | 2:239169095 | GTCTGGTAAACTCTG[A/T]GGAAGTAATTTAGAC | 9759 |
rs895803 | snp | C/T | 0.494358 | 0.0528145 | intron-variant | HDAC4 | GRCh38.p7 | 2:239191350 | CGTCTCTGGACTGGC[C/T]TAAGACCAGGCCTTG | 9759 |
rs895804 | snp | C/T | 0.310386 | 0.242597 | intron-variant | HDAC4 | GRCh38.p7 | 2:239191506 | CAGGTCCCACACTGG[C/T]TTTGTCTCCAAACCA | 9759 |
rs895805 | snp | C/T | 0.494315 | 0.0530107 | intron-variant | HDAC4 | GRCh38.p7 | 2:239191669 | CACCTGAGCTCCTGG[C/T]GCCCAGGGTGAGGGG | 9759 |
rs895806 | snp | C/T | 0.489665 | 0.0711382 | intron-variant | HDAC4 | GRCh38.p7 | 2:239191678 | TCCTGGTGCCCAGGG[C/T]GAGGGGTGCTCTCAG | 9759 |
rs895807 | snp | C/T | 0.48955 | 0.071525 | intron-variant | HDAC4 | GRCh38.p7 | 2:239191698 | GGTGCTCTCAGCTTC[C/T]CTGGCTGACTTCACT | 9759 |
rs895808 | snp | G/T | 0.445064 | 0.156365 | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239048664 | AACAGTTTTTGTTTG[G/T]TTTTTTTGCCGTGTG | 9759 |
rs895814 | snp | C/T | 0.479095 | 0.100076 | intron-variant | HDAC4 | GRCh38.p7 | 2:239147038 | GCTGGGGCCCTCCGC[C/T]CGTCCCTGCCCCGTG | 9759 |
rs895815 | snp | C/T | 0.49995 | 0.00499176 | intron-variant | HDAC4 | GRCh38.p7 | 2:239157757 | TGCACCTGGAGTTAT[C/T]TGAATTAAGAATGGG | 9759 |
rs899937 | snp | C/G | 0.455858 | 0.141853 | intron-variant, upstream-variant-2KB | HDAC4, MGC16025 | GRCh38.p7 | 2:239196975 | AGCAGTGCAGACAGA[C/G]GGAGCGCCTGCCCGG | 9759 |
rs899938 | snp | C/T | 0.422315 | 0.181128 | intron-variant, upstream-variant-2KB | HDAC4, MGC16025 | GRCh38.p7 | 2:239196758 | GGGTCTTCTGCCCAG[C/T]TCCCACCTGAGAGCT | 9759 |
rs908255 | snp | G/T | 0.305685 | 0.24372 | intron-variant | HDAC4 | GRCh38.p7 | 2:239391843 | GAGCTGAGGCACGTG[G/T]GAGCTGCGGAGGGCC | 9759 |
rs908256 | snp | A/G | 0.281841 | 0.247964 | intron-variant | HDAC4 | GRCh38.p7 | 2:239391841 | GCTGAGGCACGTGGG[A/G]GCTGCGGAGGGCCTC | 9759 |
rs908257 | snp | A/G | 0.220246 | 0.248223 | intron-variant | HDAC4 | GRCh38.p7 | 2:239391409 | TGCAGGACTTTCTGA[A/G]GCTCCTGCACCTGCT | 9759 |
rs908258 | snp | C/T | 0.499154 | 0.0205497 | intron-variant | HDAC4 | GRCh38.p7 | 2:239387392 | GCATTGCGTTGGTGG[C/T]GGCCGGCCCTGTGGT | 9759 |
rs908259 | snp | C/T | 0.22263 | 0.248497 | intron-variant | HDAC4 | GRCh38.p7 | 2:239386106 | GGTCCTGGCATCCTG[C/T]GGCTCATCATTGTCT | 9759 |
rs908260 | snp | C/T | 0.33693 | 0.2344 | intron-variant | HDAC4 | GRCh38.p7 | 2:239384580 | GTGCAGGCCGGAGTG[C/T]AGTGGGACAATCATG | 9759 |
rs908261 | snp | A/T | 0.496034 | 0.0443518 | intron-variant | HDAC4 | GRCh38.p7 | 2:239384372 | CCCACCTAGGCCACC[A/T]AAAGTTCTGGGATTA | 9759 |
rs908262 | snp | G/T | 0.303438 | 0.244222 | intron-variant | HDAC4 | GRCh38.p7 | 2:239295827 | TTTGGAGAGACAGCT[G/T]CCCTAGAACTCACAC | 9759 |
rs908263 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | HDAC4 | GRCh38.p7 | 2:239341408 | TCCAAATCAGGTGGG[A/G]CTGATTCTTCCAGCC | 9759 |
rs908265 | snp | A/G | 0.464735 | 0.128019 | intron-variant | HDAC4 | GRCh38.p7 | 2:239340592 | AGGCTGTTGTAACAG[A/G]ATGATAAGGTGCAGA | 9759 |
rs908267 | snp | A/G | 0.499295 | 0.0187567 | upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239403399 | AATTGAGAATGTTTC[A/G]TATTTTCTAACACAT | 9759 |
rs925736 | snp | C/T | 0.331179 | 0.236453 | intron-variant | HDAC4 | GRCh38.p7 | 2:239381617 | AGAAGTAAATGGCAC[C/T]GCATTTGCCCAGTAT | 9759 |
rs925737 | snp | A/G | 0.323197 | 0.239044 | intron-variant | HDAC4 | GRCh38.p7 | 2:239330556 | GCTGCCAGTGACCGC[A/G]CACAGTGGTTGAAGG | 9759 |
rs925738 | snp | A/G | 0.363985 | 0.222503 | intron-variant | HDAC4 | GRCh38.p7 | 2:239319560 | GGAGTGCCGGGTCAC[A/G]GGTAAGCTACTTTTA | 9759 |
rs925739 | snp | A/G | 0.490618 | 0.0678448 | intron-variant | HDAC4 | GRCh38.p7 | 2:239319426 | GGCCTGTGCCTGACC[A/G]CCAGCCTGCTGTGGC | 9759 |
rs938366 | snp | A/G | 0.334642 | 0.235236 | intron-variant | HDAC4 | GRCh38.p7 | 2:239341241 | CCCCACGTCTCTCTC[A/G]TGTGCTTCCATAGCA | 9759 |
rs950225 | snp | A/G | 0.288906 | 0.246954 | intron-variant | HDAC4 | GRCh38.p7 | 2:239336549 | TTACTTTAGCACCTA[A/G]CTTTTACAGTTTTTC | 9759 |
rs965837 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | HDAC4 | GRCh38.p7 | 2:239377972 | ACCAGGCATTTTGAT[A/G]TCCATAGAACTCCTA | 9759 |
rs999302 | snp | A/G | 0.33303 | 0.235809 | intron-variant | HDAC4 | GRCh38.p7 | 2:239292148 | GGCAGGCAAGGGGAC[A/G]GCCAGGATGGTAGGT | 9759 |
rs1001285 | snp | A/G | 0.422 | 0.181428 | intron-variant | HDAC4 | GRCh38.p7 | 2:239186118 | TGGTGGAAAAGCACC[A/G]TCCGAGAAGGAGAGG | 9759 |
rs1010467 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | HDAC4 | GRCh38.p7 | 2:239253678 | AACAGTTATGAAGAT[A/T]GAATAAAATCTCGCC | 9759 |
rs1015458 | snp | A/G | 0.393065 | 0.205018 | intron-variant | HDAC4 | GRCh38.p7 | 2:239234956 | TCTCAAAAATGCCCC[A/G]GCCACAGAATTCAGT | 9759 |
rs1015459 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | HDAC4 | GRCh38.p7 | 2:239235115 | GCTCCAGTGTGCTGG[A/G]GTAAAAAATAAACTG | 9759 |
rs1028117 | snp | C/G | 0.140581 | 0.224783 | intron-variant | HDAC4 | GRCh38.p7 | 2:239235589 | CGCCATCAGGAGGTT[C/G]AGGTTTTATTCTCGG | 9759 |
rs1051805 | snp | C/T | 0.0109286 | 0.0731087 | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239048955 | GCCCGCCCTCACTGG[C/T]CTTGTGACGGTTTAT | 9759 |
rs1053025 | snp | A/G | 0.498714 | 0.0253268 | intron-variant | HDAC4 | GRCh38.p7 | 2:239094088 | CAGCCGAAACGGTGC[A/G]GTGTGTGTGTAATCA | 9759 |
rs1055333 | snp | C/G | 0.359152 | 0.224913 | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239048278 | GTGACCGTCAGAAGA[C/G]GATATCATTGGTCGG | 9759 |
rs1060733 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | HDAC4, MIR4269 | GRCh38.p7 | 2:239303811 | TTCATGAGAGCATAG[A/G]CGAGTGCCGCGCCCT | 9759 |
rs1063639 | snp | C/T | 0.497778 | 0.0332559 | synonymous-codon | HDAC4 | GRCh38.p7 | 2:239082174 | TTTCTACAGCGACCC[C/T]AGCGTCCTGTACATG | 9759 |
rs1108519 | snp | C/T | 0.499527 | 0.0153681 | intron-variant | HDAC4 | GRCh38.p7 | 2:239390188 | CATCAGATAGGATCT[C/T]GCTAGGTACTGTGGC | 9759 |
rs1161474 | snp | A/G | 0.499977 | 0.00339449 | intron-variant | HDAC4 | GRCh38.p7 | 2:239209361 | GGGACCACCTCAACT[A/G]CTTCTCAGTTCTTCT | 9759 |
rs1185485 | snp | C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239075252 | TTAGAGACTGAGTTC[C/T]ttttttttttttttt | 9759 |
rs1318180 | snp | C/T | 0.49928 | 0.018956 | intron-variant | HDAC4 | GRCh38.p7 | 2:239168841 | AAGTACCCAACTGTA[C/T]ACAGTTTATTATTAA | 9759 |
rs1399629 | snp | C/T | 0.498714 | 0.0253268 | intron-variant | HDAC4 | GRCh38.p7 | 2:239336263 | TGAAATGGGACATCC[C/T]AACACCCAGAAGCCC | 9759 |
rs1403606 | snp | A/G | 0.289942 | 0.246789 | intron-variant | HDAC4 | GRCh38.p7 | 2:239254246 | AAGAAGGATGAGAGG[A/G]AGGGAGGGAGGAAAG | 9759 |
rs1403607 | snp | A/G | 0.316485 | 0.240998 | intron-variant | HDAC4 | GRCh38.p7 | 2:239254337 | CACCATGTGGGAATC[A/G]GCAAGAACAACAAAA | 9759 |
rs1403608 | snp | A/G | 0.311859 | 0.242226 | intron-variant | HDAC4 | GRCh38.p7 | 2:239260176 | GCCCCTCTGCGGACC[A/G]CGTGTCCAGACTCTG | 9759 |
rs1448429 | snp | A/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239170881 | TTAAAGGACCCCAAT[A/G]AACCTCATGAGCTTG | 9759 |
rs1448430 | snp | A/G | 0.17332 | 0.23795 | intron-variant | HDAC4 | GRCh38.p7 | 2:239171043 | CACTTCTGGTCAACT[A/G]CAAGAAGGAAAACAA | 9759 |
rs1467296 | snp | A/G | 0.446249 | 0.154875 | intron-variant | HDAC4 | GRCh38.p7 | 2:239292173 | GTAGGTGGGGCCCCA[A/G]GTGTTCCGGTGTTTT | 9759 |
rs1467297 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HDAC4 | GRCh38.p7 | 2:239292318 | AGACAAGATGCCCTC[A/G]CTCACTGCTCTCTGC | 9759 |
rs1476321 | snp | C/T | 0.496937 | 0.0390173 | intron-variant | HDAC4 | GRCh38.p7 | 2:239356243 | GTGAAAACAGTTTGA[C/T]GGAACAGTAAAAGGA | 9759 |
rs1531687 | snp | G/T | 0.199254 | 0.244796 | intron-variant | HDAC4 | GRCh38.p7 | 2:239148079 | TGTCCAGCGGCCAGC[G/T]AGGAAAGAACCCATT | 9759 |
rs1531688 | snp | G/T | 0.195837 | 0.244062 | intron-variant | HDAC4 | GRCh38.p7 | 2:239148104 | CCCATTGATGTAGCA[G/T]CAGAGAATGCACGCA | 9759 |
rs1533932 | snp | A/C | 0.464416 | 0.128553 | intron-variant | HDAC4 | GRCh38.p7 | 2:239257085 | TAAGCATTCCTATAA[A/C]CCCTTTAATAATTAT | 9759 |
rs1542232 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | HDAC4 | GRCh38.p7 | 2:239148599 | CTGCAGGAAACCCGT[C/T]ccaaccaactgatca | 9759 |
rs1567974 | snp | C/T | 0.162909 | 0.23434 | intron-variant | HDAC4 | GRCh38.p7 | 2:239358885 | ATACACGATTCTCCT[C/T]GTTCTCAGCCTTACC | 9759 |
rs1567975 | snp | C/T | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239340184 | GTGACTGGCTTGGTG[C/T]AGCTGAGGCTCAGGG | 9759 |
rs1666866 | snp | C/T | 0.482234 | 0.0925596 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239231632 | GATGCCTGAGGTAGG[C/T]GTCCTCCCCGAAGCA | 9759 |
rs1709851 | snp | G/T | 0.408179 | 0.193596 | upstream-variant-2KB, intron-variant, nc-transcript-variant | HDAC4, LOC101928111 | GRCh38.p7 | 2:239401967 | TCTACGGGCCGACCT[G/T]TAACTCAACACAAGC | 9759 |
rs1709852 | snp | A/G | 0.467946 | 0.122472 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | HDAC4, LOC101928111 | GRCh38.p7 | 2:239401581 | CCTGCACCCCATTGT[A/G]TGCCCTCTAAGCGCG | 9759 |
rs1801746 | snp | C/T | | | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239050185 | TGGCAGGGGGAGGCA[C/T]GTTTCATCTGTCAGC | 9759 |
rs1801747 | snp | A/T | | | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239048940 | CCTTGTGACGGTTTA[A/T]TCTGATTGAGAACTG | 9759 |
rs1810293 | snp | C/G | 0.498277 | 0.0293024 | upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239403447 | TTCTGTTGGAACTTA[C/G]TGTTACATTTAGGTA | 9759 |
rs1868314 | snp | A/T | 0.2768 | 0.248559 | intron-variant | HDAC4 | GRCh38.p7 | 2:239200438 | CTTTAAGGTAAAGAT[A/T]TAAAAATATTCTGTA | 9759 |
rs1962113 | snp | A/C | 0.422 | 0.181428 | intron-variant | HDAC4 | GRCh38.p7 | 2:239186421 | AAATCATCCAAACAA[A/C]AGCCTCCTAATGTAA | 9759 |
rs1973788 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | HDAC4 | GRCh38.p7 | 2:239235725 | AGGTACTCCAAGTCT[A/G]TAGGCCATGGAAACA | 9759 |
rs1979449 | snp | A/C | 0.477175 | 0.104362 | intron-variant | HDAC4 | GRCh38.p7 | 2:239076014 | TAGCAGTAGCAGGCG[A/C]GTGCCAGCGAACTCT | 9759 |
rs1992899 | snp | C/T | 0.356169 | 0.226336 | intron-variant | HDAC4 | GRCh38.p7 | 2:239172335 | CACTAAAAACATACA[C/T]TAAAGGCAAGACAAG | 9759 |
rs2017669 | snp | C/T | 0.41325 | 0.18934 | intron-variant | HDAC4 | GRCh38.p7 | 2:239340731 | GTGTGGCCCTCAGCA[C/T]GGGGAGCCCTGTGGC | 9759 |
rs2018414 | snp | C/T | 0.49753 | 0.0350569 | intron-variant | HDAC4 | GRCh38.p7 | 2:239337976 | CTTTCCTGGGATTTC[C/T]AGACCAGATCCACCT | 9759 |
rs2037554 | snp | A/T | 0.360632 | 0.224189 | intron-variant | HDAC4 | GRCh38.p7 | 2:239241341 | aagagacaccctttc[A/T]ccccaaccTGGGCAG | 9759 |
rs2037555 | snp | A/G | 0.454302 | 0.144085 | intron-variant | HDAC4 | GRCh38.p7 | 2:239241185 | CCTTTCTTGTGTGTC[A/G]GTATTGTGATGTGAA | 9759 |
rs2048764 | snp | A/G | 0.308661 | 0.24302 | intron-variant | HDAC4 | GRCh38.p7 | 2:239379682 | TGGGGCTGCCAGGGG[A/G]ATGGTGCCCAGGCTG | 9759 |
rs2048765 | snp | C/T | 0.329783 | 0.236927 | intron-variant | HDAC4 | GRCh38.p7 | 2:239286459 | GGTTTTCAACTCTCC[C/T]TGGACTTTTACTTTC | 9759 |
rs2048766 | snp | C/T | 0.456095 | 0.141508 | intron-variant | HDAC4 | GRCh38.p7 | 2:239238990 | CGTTCGATAACAGCA[C/T]GTGGATTCCCTGCGT | 9759 |
rs2048767 | snp | G/T | 0.339203 | 0.233544 | intron-variant | HDAC4 | GRCh38.p7 | 2:239239055 | TATACTGGCGGGTGG[G/T]GTGGTTTCTGACACC | 9759 |
rs2056537 | snp | C/G/T | 0.0410781 | 0.137432 | intron-variant | HDAC4 | GRCh38.p7 | 2:239233779 | ATGAGTGTGTACTTG[C/G/T]AGCAGGAAGGGCGCC | 9759 |
rs2084449 | snp | A/G | 0.318174 | 0.240525 | intron-variant | HDAC4 | GRCh38.p7 | 2:239062589 | TTATTTTAAATAACA[A/G]TAGGGAACTTCGCTT | 9759 |
rs2100171 | snp | A/C | 0.199254 | 0.244796 | intron-variant | HDAC4 | GRCh38.p7 | 2:239147807 | AATGACTAATTAAGG[A/C]GATACAACATTCCAA | 9759 |
rs2100172 | snp | A/G | 0.304188 | 0.244057 | intron-variant | HDAC4 | GRCh38.p7 | 2:239062482 | CAAAAAGGAGGAAGC[A/G]CTAGTTTTATCAAGG | 9759 |
rs2121980 | snp | C/T | 0.428333 | 0.175206 | intron-variant | HDAC4 | GRCh38.p7 | 2:239133857 | CTCTAAATTGTATTT[C/T]TCTAAATGTAACCAC | 9759 |
rs2121981 | snp | A/G | 0.303688 | 0.244167 | intron-variant | HDAC4 | GRCh38.p7 | 2:239148072 | GATGCAATGTCCAGC[A/G]GCCAGCGAGGAAAGA | 9759 |
rs2121982 | snp | C/T | 0.187685 | 0.242109 | intron-variant | HDAC4 | GRCh38.p7 | 2:239132177 | AGGGGCACATGAGTG[C/T]ACAGCCCACTTAACC | 9759 |
rs2138167 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | HDAC4 | GRCh38.p7 | 2:239283344 | AGGCCCGCACCCTGG[C/G]CACTTCTGCTGCCGG | 9759 |
rs2138168 | snp | C/T | 0.470618 | 0.117591 | intron-variant | HDAC4 | GRCh38.p7 | 2:239368417 | GCTGGCGCTGCTGCA[C/T]TTCACCTTTCTTCAC | 9759 |
rs2166895 | snp | C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239075810 | TGTCCCAGCCCAGCT[C/T]TATTCCCTGGGAAGC | 9759 |
rs2176044 | snp | G/T | 0.353803 | 0.227431 | intron-variant | HDAC4 | GRCh38.p7 | 2:239246860 | TGAGAGGATGTCCAC[G/T]GCCCAGTGGCGAGGG | 9759 |
rs2176045 | snp | C/T | 0.418491 | 0.184691 | intron-variant | HDAC4 | GRCh38.p7 | 2:239373870 | AATGAGGACGGGTCC[C/T]TGATGCCCCAATTGT | 9759 |
rs2176046 | snp | A/G | 0.4021 | 0.198407 | intron-variant | HDAC4 | GRCh38.p7 | 2:239373918 | GCTTTACTTTTTACA[A/G]TTAAGCCTTGAATCC | 9759 |
rs2176047 | snp | A/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239327201 | TTTCCTGGGGCACCT[A/G]GCTTTGCCCTGGGAG | 9759 |
rs2277885 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | HDAC4 | GRCh38.p7 | 2:239126331 | GAGCATGTGCCTCCT[C/T]GGTTCCCTCTTTCTG | 9759 |
rs2278778 | snp | A/G | 0.463153 | 0.130636 | intron-variant | HDAC4 | GRCh38.p7 | 2:239134205 | TCCAGAGCGTGGGCA[A/G]CCTCAGAGCCTGGCT | 9759 |
rs2279271 | snp | C/T | 0.409382 | 0.192607 | intron-variant, upstream-variant-2KB | HDAC4, MIR4441 | GRCh38.p7 | 2:239087384 | GTGATGCTCGCAGAC[C/T]TTGGCATCTGCACTC | 9759 |
rs2279272 | snp | A/G | 0.493293 | 0.0575177 | intron-variant | HDAC4 | GRCh38.p7 | 2:239094707 | GAGCAGATTACTGCC[A/G]CAGACTTCGAAGGGG | 9759 |
rs2279273 | snp | C/T | 0.24947 | 0.249999 | intron-variant | HDAC4 | GRCh38.p7 | 2:239095075 | TGGGGGGGAGGGAGA[C/T]GGTCAGAGAGGCCAA | 9759 |
rs2279274 | snp | A/G | 0.35207 | 0.228214 | intron-variant | HDAC4 | GRCh38.p7 | 2:239095128 | ACAGGCCCTGGGCGC[A/G]CTCCGGGGTCTTCAG | 9759 |
rs2290084 | snp | C/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239090194 | GAGCCCACGGAACCT[C/G]AGCTGCTCTGCCCAG | 9759 |
rs2290085 | snp | A/G | | | missense | HDAC4 | GRCh38.p7 | 2:239090029 | GAGCTGGTCTTCAAG[A/G]TGGCCACAGGGGAGC | 9759 |
rs2290086 | snp | A/G | 9.88419e-05 | 0.00702931 | synonymous-codon, utr-variant-5-prime, intron-variant | HDAC4 | GRCh38.p7 | 2:239144646 | CTTTCCTGCGTAACA[A/G]GGGGCTGCTCCGTCT | 9759 |
rs2290087 | snp | A/G | 0.238485 | 0.249735 | intron-variant | HDAC4 | GRCh38.p7 | 2:239144721 | GTTCAGAAGCTGCAC[A/G]AAAAGGAGATGTCAT | 9759 |
rs2290088 | snp | C/T | 0.427575 | 0.175975 | intron-variant | HDAC4 | GRCh38.p7 | 2:239144830 | TTTGCTCAACACTGC[C/T]GTGTTGCTGCAGGGG | 9759 |
rs2290089 | snp | A/C | 0.488666 | 0.0744214 | intron-variant | HDAC4 | GRCh38.p7 | 2:239164099 | AGGGGTTTTAATGAG[A/C]GGTTTTCTTCCCATC | 9759 |
rs2290090 | snp | A/G | 0.350982 | 0.228698 | intron-variant | HDAC4 | GRCh38.p7 | 2:239164185 | TTATTGTTAGCTAAC[A/G]CAAAACCCACTTCTG | 9759 |
rs2290091 | snp | A/G | 0.0640484 | 0.167099 | intron-variant | HDAC4 | GRCh38.p7 | 2:239189811 | AGGCCTGGCCCACCC[A/G]CAGCCCCGCACCGCG | 9759 |
rs2290092 | snp | C/T | 0.176766 | 0.239033 | intron-variant | HDAC4 | GRCh38.p7 | 2:239189825 | CGCAGCCCCGCACCG[C/T]GCCTCACCTTGATGT | 9759 |
rs2291186 | snp | G/T | 0.423726 | 0.179776 | intron-variant | HDAC4 | GRCh38.p7 | 2:239094233 | TTCTCATGGCCGCCC[G/T]CGCTATTGCCACCCC | 9759 |
rs2291187 | snp | C/T | 0.146985 | 0.227789 | intron-variant | HDAC4 | GRCh38.p7 | 2:239094313 | TATTGAGAAGTTTGA[C/T]TGCAAGACCTGACCC | 9759 |
rs2291188 | snp | C/T | 0.352287 | 0.228117 | intron-variant | HDAC4 | GRCh38.p7 | 2:239094481 | TCAGTTCGTAGAAGC[C/T]GGCACAGACCAGTGA | 9759 |
rs2307755 | in-del | -/CCT | 0.5 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239222800 | TTTGCTTTGTGATCT[-/CCT]TTCGTCCTCACAGCC | 9759 |
rs2307756 | in-del | -/TG | 0.334642 | 0.235236 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239228408 | GGAGGGAGCTGTCAC[-/TG]TGAGAGTTAGGAGGA | 9759 |
rs2411424 | snp | A/G | 0.23846 | 0.249734 | intron-variant | HDAC4 | GRCh38.p7 | 2:239170734 | AACAACTAGGGCAGC[A/G]TGGAACACCAGGGCC | 9759 |
rs2411425 | snp | A/G | 0.496842 | 0.0396107 | intron-variant | HDAC4 | GRCh38.p7 | 2:239170890 | CCCAATAAACCTCAT[A/G]AGCTTGTGCGTAGGA | 9759 |
rs2411426 | snp | A/T | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239172295 | GCTGGTGAAAAAAAA[A/T]ATATATATATATATA | 9759 |
rs2411427 | snp | A/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239172297 | TGGTGAAAAAAAATA[A/T]ATATATATATATATA | 9759 |
rs2411428 | snp | A/G | 0.137187 | 0.223099 | intron-variant | HDAC4 | GRCh38.p7 | 2:239190700 | CTCCTGGCTCTTGGC[A/G]CAAGTGCGTTCCTCT | 9759 |
rs2411429 | snp | A/G | 0.310386 | 0.242597 | intron-variant | HDAC4 | GRCh38.p7 | 2:239192232 | AGCAGGGGTCCACCC[A/G]CCCCCCACCCCACAC | 9759 |
rs2411843 | snp | A/C | 0.422944 | 0.180528 | intron-variant | HDAC4 | GRCh38.p7 | 2:239373274 | CATCTCTCTTGCCAT[A/C]TTCTGCCAAGCTAGG | 9759 |
rs2411844 | snp | A/C | 0.337386 | 0.23423 | intron-variant | HDAC4 | GRCh38.p7 | 2:239379259 | AGCCAGGTGACCAAC[A/C]CAGGAAGGTGGGTCC | 9759 |
rs2411845 | snp | C/T | 0.246769 | 0.249979 | intron-variant | HDAC4 | GRCh38.p7 | 2:239389135 | CCAATCAGCACTCTG[C/T]GTCTAGCTAAAGGAT | 9759 |
rs2411846 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | HDAC4 | GRCh38.p7 | 2:239389200 | CCAATCAGTAGGACG[C/T]GGGTGGGGACAAATA | 9759 |
rs2411847 | snp | A/C/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239391906 | CAGAACTTCGTCAGA[A/C/G]CGCAGCCCGCGTGTG | 9759 |
rs2411848 | snp | A/C | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239391907 | AGAACTTCGTCAGAA[A/C]GCAGCCCGCGTGTGC | 9759 |
rs2411849 | snp | A/C | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239391909 | AACTTCGTCAGAACG[A/C]AGCCCGCGTGTGCTG | 9759 |
rs2411850 | snp | C/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239391911 | CTTCGTCAGAACGCA[C/G]CCCGCGTGTGCTGAA | 9759 |
rs2411851 | snp | C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239391912 | TTCGTCAGAACGCAG[C/T]CCGCGTGTGCTGAAG | 9759 |
rs2411852 | snp | C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239391913 | TCGTCAGAACGCAGC[C/T]CGCGTGTGCTGAAGC | 9759 |
rs2411853 | snp | C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239391916 | TCAGAACGCAGCCCG[C/T]GTGTGCTGAAGCTGG | 9759 |
rs2411854 | snp | C/G | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239391917 | CAGAACGCAGCCCGC[C/G]TGTGCTGAAGCTGGC | 9759 |
rs2411855 | snp | A/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239391918 | AGAACGCAGCCCGCG[A/T]GTGCTGAAGCTGGCA | 9759 |
rs2594709 | snp | A/G | 0.169435 | 0.236663 | | | GRCh38.p7 | 2:239231647 | TGTCCTCCCCGAAGC[A/G]CCCCTCTCCTCAACC | 9759 |
rs2898716 | snp | G/T | 0.417196 | 0.185864 | intron-variant | HDAC4 | GRCh38.p7 | 2:239127215 | CTTCGAGCACTGATT[G/T]TATGCACAAAGATGG | 9759 |
rs2898824 | snp | A/G | 0.490453 | 0.0684267 | intron-variant | HDAC4 | GRCh38.p7 | 2:239321987 | AGATTTGTTTAAGCG[A/G]AAGTACACTCCACAG | 9759 |
rs2898825 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | HDAC4 | GRCh38.p7 | 2:239335010 | agcctggaagacaga[A/G]caagactccatctca | 9759 |
rs2931203 | snp | A/T | 0.357451 | 0.225731 | upstream-variant-2KB, downstream-variant-500B, intron-variant | HDAC4, LOC101928111 | GRCh38.p7 | 2:239402622 | AGGATTCTCAAAAAC[A/T]TACAATCACGAGAAA | 9759 |
rs2931204 | snp | C/T | 0.206029 | 0.246103 | intron-variant | HDAC4 | GRCh38.p7 | 2:239398076 | CTTCAGTTCCCCCAT[C/T]CCCAGCTAGTCATCA | 9759 |
rs2931206 | snp | C/G | 0.46754 | 0.123192 | intron-variant, upstream-variant-2KB | HDAC4, LOC101928111 | GRCh38.p7 | 2:239400138 | CCCCCGAGCGGGACC[C/G]GGCCCCGTCTCGGCC | 9759 |
rs3080332 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239156895 | CCACCTCAACAGACA[-/CA]CCTTTTCCCTAGGGT | 9759 |
rs3084829 | in-del | -/CCCTGGA | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239289595 | GTCTTTTCTTCTGGA[-/CCCTGGA]AATCCAGGCTGGGGA | 9759 |
rs3084851 | in-del | -/CG | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239385303 | CATGGGGGCACACAG[-/CG]GGCTGGCTGCTCTCA | 9759 |
rs3215239 | in-del | -/C | 0.495354 | 0.0479746 | upstream-variant-2KB, nc-transcript-variant | HDAC4, LOC101928111 | GRCh38.p7 | 2:239402211 | TCGAAGCGAACGCGC[-/C]ATCTCCGCCAGGTCC | 9759 |
rs3752755 | snp | A/G | 0.416708 | 0.186302 | intron-variant | HDAC4 | GRCh38.p7 | 2:239082549 | TGATCAGATGGCTTC[A/G]TCTGGGAAATGGTGG | 9759 |
rs3752756 | snp | C/G | 0.0755793 | 0.179102 | intron-variant | HDAC4 | GRCh38.p7 | 2:239082502 | AACTCCAGCCCCATC[C/G]GCTGCTGGAGTCAGG | 9759 |
rs3752758 | snp | A/G | 0.423413 | 0.180077 | intron-variant | HDAC4 | GRCh38.p7 | 2:239081769 | CACAGGACACCCTCC[A/G]GCAAGGGGCTCTGTC | 9759 |
rs3752759 | snp | A/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239081768 | ACAGGACACCCTCCG[A/G]CAAGGGGCTCTGTCC | 9759 |
rs3752804 | snp | C/T | 0.497984 | 0.0316851 | intron-variant | HDAC4 | GRCh38.p7 | 2:239107794 | GAGGTGGGAGCGAAA[C/T]ATCAGGAAAGGTCAC | 9759 |
rs3762502 | snp | A/G | | | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239193567 | CTGAGCAAGGACCCA[A/G]AGGTCTGGGTGCAGG | 9759 |
rs3791360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HDAC4 | GRCh38.p7 | 2:239062500 | TTCCTCCTTTTTGAC[A/G]TGTTTAAGTAAAAGA | 9759 |
rs3791362 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HDAC4 | GRCh38.p7 | 2:239063180 | CCCCATCCTCCCAAG[A/C]CGGGCCGTGGCCCTG | 9759 |
rs3791363 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HDAC4 | GRCh38.p7 | 2:239066078 | AGGCCCTGCTGGGAG[A/C]AGGGAGGCCCGGGCC | 9759 |
rs3791364 | snp | C/G | 0.436205 | 0.16837 | intron-variant | HDAC4 | GRCh38.p7 | 2:239076291 | GCCACTCTGCTTCCT[C/G]GAAAGGCCATCGCTC | 9759 |
rs3791365 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HDAC4 | GRCh38.p7 | 2:239076533 | ACTCACCACACCTTC[C/T]GTCAACACAAGCCTC | 9759 |
rs3791366 | snp | C/T | 0.434831 | 0.168337 | intron-variant | HDAC4 | GRCh38.p7 | 2:239076857 | CCTCATCCACCCCCA[C/T]CTGAACCTTCTCCCG | 9759 |
rs3791367 | snp | C/T | 0.441432 | 0.160792 | intron-variant | HDAC4 | GRCh38.p7 | 2:239077768 | GCAGACATCAGGCGC[C/T]GCGACTCCTAAAACA | 9759 |
rs3791368 | snp | C/G/T | 0.0663309 | 0.169604 | intron-variant | HDAC4 | GRCh38.p7 | 2:239078414 | TCCCCGGGGGGCCCC[C/G/T]GTGGGGGAGAAGAGC | 9759 |
rs3791369 | snp | A/C | 0.435694 | 0.167385 | intron-variant | HDAC4 | GRCh38.p7 | 2:239078822 | CAAGAGCCGAAGGCA[A/C]CACTGAGAAACGCCT | 9759 |
rs3791370 | snp | A/G | 0.482234 | 0.0925596 | intron-variant | HDAC4 | GRCh38.p7 | 2:239079635 | ACAAGACGTTTACAC[A/G]TGTCCTTGTGAAGGG | 9759 |
rs3791371 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HDAC4 | GRCh38.p7 | 2:239082947 | TGCCTGAGAAGACAG[C/T]ATGCAGCCCTGATGT | 9759 |
rs3791372 | snp | C/T | 0.498525 | 0.0271165 | intron-variant | HDAC4 | GRCh38.p7 | 2:239083111 | GAGGCTTTCCCGACA[C/T]GTGGCTTCACACTGA | 9759 |
rs3791373 | snp | A/G | 0.466721 | 0.124627 | intron-variant | HDAC4 | GRCh38.p7 | 2:239083142 | GATGACCCTGTCCGC[A/G]TGGTGTGTACATGGG | 9759 |
rs3791374 | snp | A/G | 0.490063 | 0.0697833 | intron-variant | HDAC4 | GRCh38.p7 | 2:239083195 | GGGAGCACGCCACAC[A/G]GGGTCTACGCAGCCT | 9759 |
rs3791375 | snp | A/G | 0.399073 | 0.200692 | intron-variant | HDAC4 | GRCh38.p7 | 2:239083204 | CCACACAGGGTCTAC[A/G]CAGCCTGTCTGCGTG | 9759 |
rs3791376 | snp | C/T | 0.356811 | 0.226034 | intron-variant | HDAC4 | GRCh38.p7 | 2:239087980 | CTCGGGACCAGGACC[C/T]GCTAGGTGGCCACTG | 9759 |
rs3791377 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HDAC4 | GRCh38.p7 | 2:239088370 | GAGCCGGACGCCGCA[A/G]GGACCAGGCTCAGGA | 9759 |
rs3791378 | snp | C/G | 0.39709 | 0.20215 | intron-variant | HDAC4 | GRCh38.p7 | 2:239091288 | GATGAAATACACAGC[C/G]CTTGGGCTGGCCCCA | 9759 |
rs3791379 | snp | A/G | 0.351635 | 0.228408 | intron-variant | HDAC4 | GRCh38.p7 | 2:239095978 | AGGCTCCTTTATCCA[A/G]CGTGGGACCCCACTT | 9759 |
rs3791380 | snp | A/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239096948 | CAGGGAGCAGGGCAG[A/G]AGGCAGGAGGCAGGG | 9759 |
rs3791381 | snp | A/G | 0.369346 | 0.219673 | intron-variant | HDAC4 | GRCh38.p7 | 2:239096963 | GAGGCAGGAGGCAGG[A/G]GGCAGCAGCTGCAGC | 9759 |
rs3791382 | snp | C/G | 0.490673 | 0.0676508 | intron-variant | HDAC4 | GRCh38.p7 | 2:239097116 | GTTTTCCAGACAAAG[C/G]CCTACGTGCTCGGAG | 9759 |
rs3791383 | snp | A/G | 0.369346 | 0.219673 | intron-variant | HDAC4 | GRCh38.p7 | 2:239097142 | CGGAGGAGCCAGCCT[A/G]TGTCGGAGGGAGCCC | 9759 |
rs3791384 | snp | C/T | 0.369754 | 0.219451 | intron-variant | HDAC4 | GRCh38.p7 | 2:239097588 | ACAGCAAGTAGTGGA[C/T]GTGGGGCTGACCATG | 9759 |
rs3791385 | snp | C/T | 0.369754 | 0.219451 | intron-variant | HDAC4 | GRCh38.p7 | 2:239097604 | GTGGGGCTGACCATG[C/T]GGGGAAGCGGCCTGC | 9759 |
rs3791386 | snp | A/G | 0.27893 | 0.24832 | intron-variant | HDAC4 | GRCh38.p7 | 2:239097613 | ACCATGCGGGGAAGC[A/G]GCCTGCACGCCGGAC | 9759 |
rs3791387 | snp | A/G | 0.351635 | 0.228408 | intron-variant | HDAC4 | GRCh38.p7 | 2:239098263 | CCAAGCCCAGGCCAC[A/G]AAACGTTCCAGCCTG | 9759 |
rs3791388 | snp | A/G | 0.133093 | 0.220981 | intron-variant | HDAC4 | GRCh38.p7 | 2:239098511 | GGCCCAGCTCTGCCC[A/G]GATGCAGCACCCTGC | 9759 |
rs3791389 | snp | A/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239098579 | GACGCCTAGGGCAGC[A/G]GCCAGCCTGCCTCAG | 9759 |
rs3791390 | snp | A/G | 0.32153 | 0.239548 | intron-variant | HDAC4 | GRCh38.p7 | 2:239098601 | CTGCCTCAGGCCCAC[A/G]AGCCAATTCAGCCAC | 9759 |
rs3791391 | snp | A/G | 0.369346 | 0.219673 | intron-variant | HDAC4 | GRCh38.p7 | 2:239098813 | ATACTTAGACTGATG[A/G]TAATGAAGTTTCTGG | 9759 |
rs3791392 | snp | C/T | 0.369142 | 0.219784 | intron-variant | HDAC4 | GRCh38.p7 | 2:239099237 | AAAGACTGAAGGTGG[C/T]AGGGGATGGACCAAC | 9759 |
rs3791393 | snp | A/G | 0.369142 | 0.219784 | intron-variant | HDAC4 | GRCh38.p7 | 2:239099278 | TTGAAAATGGATGAA[A/G]GTGTCAGGAGCAGCC | 9759 |
rs3791394 | snp | C/T | 0.368119 | 0.220336 | intron-variant | HDAC4 | GRCh38.p7 | 2:239099374 | CTGATGCTTTGAGGC[C/T]GCTCAGCAACTCCCA | 9759 |
rs3791395 | snp | C/T | 0.368938 | 0.219895 | intron-variant | HDAC4 | GRCh38.p7 | 2:239099571 | AGGGACAGCACACTC[C/T]AGCCTCAGTGCCTCG | 9759 |
rs3791396 | snp | C/T | 0.369958 | 0.21934 | intron-variant | HDAC4 | GRCh38.p7 | 2:239099592 | CAGTGCCTCGATGCA[C/T]GGCCTTTGTCCACCC | 9759 |
rs3791397 | snp | A/T | 0.492871 | 0.0592773 | intron-variant | HDAC4 | GRCh38.p7 | 2:239101030 | GTCCATAGCCTCTGC[A/T]GTTGCTGAGCCTGAG | 9759 |
rs3791398 | snp | A/G | 0.362104 | 0.223456 | intron-variant | HDAC4 | GRCh38.p7 | 2:239103970 | AGGGACGGATGCTCT[A/G]CGGGTTCTCTTCTCA | 9759 |
rs3791399 | snp | A/G | 0.490231 | 0.0692021 | intron-variant | HDAC4 | GRCh38.p7 | 2:239104065 | GTGACACGGCTTCCG[A/G]TGGTAAAAAACGACT | 9759 |
rs3791400 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | HDAC4 | GRCh38.p7 | 2:239106318 | ATCCCCTGGCCTCAG[C/T]GGAACCTCCTGGGGG | 9759 |
rs3791401 | snp | C/T | 0.308908 | 0.242961 | intron-variant | HDAC4 | GRCh38.p7 | 2:239106768 | ACCTGCAGGGCGGGA[C/T]CCTGCAGAAACTAAG | 9759 |
rs3791402 | snp | C/T | 0.384401 | 0.210799 | intron-variant | HDAC4 | GRCh38.p7 | 2:239106866 | TGGGCCCTGGGCTGT[C/T]GGGTGTCCAGGACTG | 9759 |
rs3791403 | snp | C/T | 0.367708 | 0.220556 | intron-variant | HDAC4 | GRCh38.p7 | 2:239106964 | TGTGGGGAGTGGACA[C/T]AGCAGGTCTCTACTG | 9759 |
rs3791404 | snp | C/T | 0.499539 | 0.0151687 | intron-variant | HDAC4 | GRCh38.p7 | 2:239106973 | TGGACATAGCAGGTC[C/T]CTACTGGTGGGCCCT | 9759 |
rs3791405 | snp | A/G | 0.490943 | 0.0666801 | intron-variant | HDAC4 | GRCh38.p7 | 2:239108588 | CTTCTAGAAGGAGGC[A/G]ACTCTAGCCCCCTAC | 9759 |
rs3791406 | snp | C/T | 0.490997 | 0.0664859 | intron-variant | HDAC4 | GRCh38.p7 | 2:239108788 | ACAGGTCTACTTAAC[C/T]TCTGACTGTGAAAAG | 9759 |
rs3791407 | snp | C/T | 0.252421 | 0.249988 | intron-variant | HDAC4 | GRCh38.p7 | 2:239108853 | AGCATGGACGGGCCC[C/T]CAGGGTGCGGCAGCC | 9759 |
rs3791408 | snp | C/T | 0.491316 | 0.0653198 | intron-variant | HDAC4 | GRCh38.p7 | 2:239108895 | TCCTGGTGGGGGCCC[C/T]AGAACCAACTGGGCC | 9759 |
rs3791409 | snp | C/G | 0.499477 | 0.0161657 | intron-variant | HDAC4 | GRCh38.p7 | 2:239108910 | CAGAACCAACTGGGC[C/G]GGCAGCCTGGGGCTC | 9759 |
rs3791410 | snp | A/G | 0.251578 | 0.249995 | intron-variant | HDAC4 | GRCh38.p7 | 2:239108920 | TGGGCCGGCAGCCTG[A/G]GGCTCTGCAGCAGGA | 9759 |
rs3791411 | snp | C/T | 0.249603 | 0.25 | intron-variant | HDAC4 | GRCh38.p7 | 2:239109066 | GGCCAGGTGGCCCTC[C/T]GGGGCACAGCTCTGC | 9759 |
rs3791412 | snp | A/G | 0.490836 | 0.0670685 | intron-variant | HDAC4 | GRCh38.p7 | 2:239109392 | CCCACTTGTGTTCCT[A/G]TTACTGGGAACACAG | 9759 |
rs3791413 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | HDAC4 | GRCh38.p7 | 2:239109700 | TGTGTGTGGGCATGG[A/C]TGTGCTTGGGAGTTT | 9759 |
rs3791414 | snp | C/T | 0.270621 | 0.249148 | intron-variant | HDAC4 | GRCh38.p7 | 2:239110518 | TCCTGTGACCTTCCA[C/T]GGTTTTCTTTCTGAG | 9759 |
rs3791416 | snp | A/G | 0.427271 | 0.176281 | intron-variant | HDAC4 | GRCh38.p7 | 2:239112491 | GGACCTTTGGGGCCT[A/G]GAGCAGGCCTGCTGG | 9759 |
rs3791417 | snp | A/G | 0.388587 | 0.208071 | intron-variant | HDAC4 | GRCh38.p7 | 2:239112651 | AGAGTGGAGTGGAGG[A/G]AGCAGGGCAGAGATG | 9759 |
rs3791418 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | HDAC4 | GRCh38.p7 | 2:239113463 | GGGCTGGAGGTGCCC[C/T]GCCTTATGTTTACCT | 9759 |
rs3791419 | snp | A/C | 0.430583 | 0.172886 | intron-variant | HDAC4 | GRCh38.p7 | 2:239113682 | CCATTTCTTATCAGC[A/C]TAATAATAGCACACT | 9759 |
rs3791420 | snp | A/C | 0.248755 | 0.249997 | intron-variant | HDAC4 | GRCh38.p7 | 2:239113696 | CCTAATAATAGCACA[A/C]TGAATTTCAGATCTT | 9759 |
rs3791421 | snp | C/T | 0.218151 | 0.247963 | intron-variant | HDAC4 | GRCh38.p7 | 2:239116561 | TGACAGCATGGCTCC[C/T]GGGAGGCCCCCACCT | 9759 |
rs3791422 | snp | C/T | 0.490287 | 0.0690083 | intron-variant | HDAC4 | GRCh38.p7 | 2:239116708 | GCCTCTGCTGAAGAG[C/T]CCCTCCATCGTGTGG | 9759 |
rs3791423 | snp | A/G | 0.139564 | 0.224285 | intron-variant | HDAC4 | GRCh38.p7 | 2:239116991 | GTATCCATCTTTCCT[A/G]CAGTCTGCAGTTCCC | 9759 |
rs3791424 | snp | A/G | 0.491987 | 0.0627894 | intron-variant | HDAC4 | GRCh38.p7 | 2:239117300 | GCCCTGCTGCAGACA[A/G]GCCAGAGGTTGAAAG | 9759 |
rs3791425 | snp | A/C | 0.232359 | 0.249377 | intron-variant | HDAC4 | GRCh38.p7 | 2:239117423 | CTGCATATGGAGAGG[A/C]AAGAGAGGGTGGCCA | 9759 |
rs3791426 | snp | A/G | 0.499977 | 0.00339449 | intron-variant | HDAC4 | GRCh38.p7 | 2:239117705 | AAAGAACGTCCCACA[A/G]TCCCAAAGTCCCAGA | 9759 |
rs3791427 | snp | A/G | 0.220843 | 0.248294 | intron-variant | HDAC4 | GRCh38.p7 | 2:239117956 | CCCTTAGAGCACTGC[A/G]TGCTGCTCCACACTC | 9759 |
rs3791428 | snp | C/T | 0.321053 | 0.23969 | intron-variant | HDAC4 | GRCh38.p7 | 2:239118750 | AGACTTTCACAAAGC[C/T]GGGGAGAAACAAGTT | 9759 |
rs3791429 | snp | A/C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239118794 | TAGCAACATTGTCCC[A/C/T]ATTTGCTCTGACAGG | 9759 |
rs3791430 | snp | A/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239119148 | GGTGCAGTCTGATGT[A/G]TAACGGGATGTGACT | 9759 |
rs3791431 | snp | A/G | 0.231775 | 0.249335 | intron-variant | HDAC4 | GRCh38.p7 | 2:239119352 | GCAGCAGCCAGGACG[A/G]GCCTTCAGGAAGCAA | 9759 |
rs3791432 | snp | A/G | 0.347473 | 0.230215 | intron-variant | HDAC4 | GRCh38.p7 | 2:239119488 | AAGGGTGCGGGGACC[A/G]GAGCTCAGGGCTGAG | 9759 |
rs3791433 | snp | C/G | 0.495855 | 0.045338 | intron-variant | HDAC4 | GRCh38.p7 | 2:239120514 | AGGCACAGGCACACA[C/G]AGACAAGGAGAGGAG | 9759 |
rs3791434 | snp | A/G | 0.499741 | 0.0113788 | intron-variant | HDAC4 | GRCh38.p7 | 2:239120582 | AAAGGGCAAGGGGAG[A/G]AGGAGGAAGGTGGGG | 9759 |
rs3791435 | snp | C/T | 0.26818 | 0.249338 | intron-variant | HDAC4 | GRCh38.p7 | 2:239120639 | AAATAGGGGGAGGGG[C/T]GGGGGAGGAAGGCTA | 9759 |
rs3791436 | snp | C/T | 0.273587 | 0.248885 | intron-variant | HDAC4 | GRCh38.p7 | 2:239120673 | CCTTAGAGGGGACCC[C/T]GTGGGGCTGCCCCAT | 9759 |
rs3791437 | snp | C/G | 0.287346 | 0.247195 | intron-variant | HDAC4 | GRCh38.p7 | 2:239120713 | GACCGAAGTGGTGTG[C/G]CTGCCTTTCTTTAGC | 9759 |
rs3791438 | snp | A/G | 0.249886 | 0.25 | intron-variant | HDAC4 | GRCh38.p7 | 2:239120730 | TGCCTTTCTTTAGCA[A/G]CCCAGGGGCCATTCT | 9759 |
rs3791439 | snp | C/G | 0.277067 | 0.24853 | intron-variant | HDAC4 | GRCh38.p7 | 2:239121459 | CGCGTCTACCGTGCT[C/G]TGCATCAGGAGACCT | 9759 |
rs3791440 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HDAC4 | GRCh38.p7 | 2:239121476 | GCATCAGGAGACCTC[C/T]CCACTGTTCCAAGGG | 9759 |
rs3791441 | snp | A/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239121522 | TCCCCGGCTGGCTGC[A/G]GATGGCGTGTGCTGC | 9759 |
rs3791442 | snp | C/T | 0.499767 | 0.0107802 | intron-variant | HDAC4 | GRCh38.p7 | 2:239121591 | TTCCCAGGTCTTTTT[C/T]CTCCCTTTCACGAGG | 9759 |
rs3791443 | snp | C/T | 0.496681 | 0.0405994 | intron-variant | HDAC4 | GRCh38.p7 | 2:239121602 | TTTTCCTCCCTTTCA[C/T]GAGGATGAAGCCTCT | 9759 |
rs3791444 | snp | C/T | 0.160609 | 0.233472 | intron-variant | HDAC4 | GRCh38.p7 | 2:239121930 | GCTGGCTTTGGGAGG[C/T]GAGCCGGACGCGGGC | 9759 |
rs3791445 | snp | C/T | 0.414576 | 0.188188 | intron-variant | HDAC4 | GRCh38.p7 | 2:239123438 | GTGGTGTCCAGTGGG[C/T]AGCAGGGGCCAGGCT | 9759 |
rs3791446 | snp | C/T | 0.432063 | 0.171327 | intron-variant | HDAC4 | GRCh38.p7 | 2:239123654 | CGCAATCAAAGCCTT[C/T]GACCACTGCGCCAGG | 9759 |
rs3791447 | snp | G/T | 0.203882 | 0.245709 | intron-variant | HDAC4 | GRCh38.p7 | 2:239126140 | CAGGACGTGGTCCAG[G/T]GGAACTCACATGGGC | 9759 |
rs3791448 | snp | C/T | 0.312104 | 0.242163 | intron-variant | HDAC4 | GRCh38.p7 | 2:239126848 | GGCTCGCTAACTGGG[C/T]CCCTTCCAGCTGAGG | 9759 |
rs3791449 | snp | G/T | 0.312104 | 0.242163 | intron-variant | HDAC4 | GRCh38.p7 | 2:239126885 | GCCGTGAGCTGGTGC[G/T]TTGGGACTATAGGAA | 9759 |
rs3791451 | snp | C/T | 0.164546 | 0.234942 | intron-variant | HDAC4 | GRCh38.p7 | 2:239127355 | TTTTGATTAAAAGAA[C/T]CCATTTTGATAGATG | 9759 |
rs3791452 | snp | G/T | 0.417359 | 0.185718 | intron-variant | HDAC4 | GRCh38.p7 | 2:239127445 | TTTCCTTCTGCATGC[G/T]TTCATCGAGATATAT | 9759 |
rs3791453 | snp | C/T | 0.312593 | 0.242037 | intron-variant | HDAC4 | GRCh38.p7 | 2:239127624 | AAAATGACCCTGACC[C/T]GCTCAAGGGCATCTG | 9759 |
rs3791454 | snp | C/T | 0.423881 | 0.179625 | intron-variant | HDAC4 | GRCh38.p7 | 2:239127951 | CTTCTCAAGTCCCTT[C/T]GCAGGGGCTATTTCT | 9759 |
rs3791455 | snp | C/T | 0.148996 | 0.228688 | intron-variant | HDAC4 | GRCh38.p7 | 2:239128638 | GTCAGTCACACAAAG[C/T]TGCTTTCAGGGGACG | 9759 |
rs3791456 | snp | C/G/T | 0.0493649 | 0.150668 | intron-variant | HDAC4 | GRCh38.p7 | 2:239128832 | CAGAGGAGAAGGACA[C/G/T]GCCAACTTCATAGGA | 9759 |
rs3791457 | snp | C/T | 0.148326 | 0.228391 | intron-variant | HDAC4 | GRCh38.p7 | 2:239128967 | CCTCCCGCCATCCTC[C/T]GCATGGGCCCAGGAA | 9759 |
rs3791458 | snp | G/T | 0.486725 | 0.0803809 | intron-variant | HDAC4 | GRCh38.p7 | 2:239129227 | ACACCCTACCCCTGG[G/T]TATCCTTGAAAAGCA | 9759 |
rs3791459 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | HDAC4 | GRCh38.p7 | 2:239129620 | ACCCTGGCTCCTGAG[C/T]TGACCCTGGCTCCTG | 9759 |
rs3791460 | snp | C/T | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239130104 | TTTAAAATCCTTCCA[C/T]TGAGAAGCAAACCAG | 9759 |
rs3791461 | snp | A/G | 0.154993 | 0.231244 | intron-variant | HDAC4 | GRCh38.p7 | 2:239130269 | GGACCACAGCCTCGC[A/G]TGCCAATTATAGGAC | 9759 |
rs3791462 | snp | C/T | 0.499942 | 0.00539106 | intron-variant | HDAC4 | GRCh38.p7 | 2:239130558 | CACCTGTCCTTAAGA[C/T]GCTGGTGGCATGCTC | 9759 |
rs3791463 | snp | C/T | 0.426507 | 0.177046 | intron-variant | HDAC4 | GRCh38.p7 | 2:239130632 | GAGGCATACACATCT[C/T]CCTCCACCTGTGCCC | 9759 |
rs3791464 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HDAC4 | GRCh38.p7 | 2:239132849 | AGGCACATTTTACGT[A/T]TTTAAAGACAGGCGA | 9759 |
rs3791465 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | HDAC4 | GRCh38.p7 | 2:239132965 | CTCCAGAGAGATCCG[C/T]GTGCCTGCCACTGTG | 9759 |
rs3791466 | snp | C/T | 0.145978 | 0.227331 | intron-variant | HDAC4 | GRCh38.p7 | 2:239133121 | ACAAAACAAAGATTG[C/T]GCCATTTGGCTTCTG | 9759 |
rs3791467 | snp | A/G | 0.160609 | 0.233472 | intron-variant | HDAC4 | GRCh38.p7 | 2:239137539 | GGCTTCCCTGGGTCC[A/G]GGGGGCCTTCAAGGT | 9759 |
rs3791468 | snp | C/T | 0.318174 | 0.240525 | intron-variant | HDAC4 | GRCh38.p7 | 2:239137640 | GCTCCCCCCACATCC[C/T]CATCCACTCGAGACA | 9759 |
rs3791469 | snp | C/T | 0.161596 | 0.233848 | intron-variant | HDAC4 | GRCh38.p7 | 2:239137733 | GCCATGAAGCACAGG[C/T]GTTCTCACAGACCCG | 9759 |
rs3791470 | snp | C/T | 0.146314 | 0.227484 | intron-variant | HDAC4 | GRCh38.p7 | 2:239137820 | AAAGGCTGCCCGTGC[C/T]CACTCTAATGAACAT | 9759 |
rs3791471 | snp | C/T | 0.311369 | 0.242351 | intron-variant | HDAC4 | GRCh38.p7 | 2:239137929 | TTCATTTACGTATCG[C/T]GATTTCTAAAAATTA | 9759 |
rs3791472 | snp | C/T | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239137973 | ATGATGCAGACCCAC[C/T]CAAACAAGGCACTGT | 9759 |
rs3791473 | snp | A/G | 0.317933 | 0.240593 | intron-variant | HDAC4 | GRCh38.p7 | 2:239138037 | ATTTTAAATAAAAAC[A/G]TGTATCTAGGACCAC | 9759 |
rs3791474 | snp | C/T | 0.392325 | 0.205532 | intron-variant | HDAC4 | GRCh38.p7 | 2:239138792 | TCCCTGGGCCTGGCA[C/T]AAGGCGCTCGGGACA | 9759 |
rs3791475 | snp | C/G | 0.486 | 0.0824865 | intron-variant | HDAC4 | GRCh38.p7 | 2:239138867 | GGAGCGAGGTCCTCG[C/G]ACCTGCTGCCCTGGA | 9759 |
rs3791476 | snp | C/T | 0.161267 | 0.233723 | intron-variant | HDAC4 | GRCh38.p7 | 2:239140039 | ACCAATTTTATACCT[C/T]GTTTGATTTTCAAGA | 9759 |
rs3791477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HDAC4 | GRCh38.p7 | 2:239140456 | CCCTTCACCTCTGAA[A/G]GGGTCTGCTGCTATT | 9759 |
rs3791478 | snp | C/T | 0.341909 | 0.232492 | intron-variant | HDAC4 | GRCh38.p7 | 2:239142443 | GTGCCGGCCAGGAGA[C/T]GCACAACCCTCTGCC | 9759 |
rs3791479 | snp | C/G | 0.427727 | 0.175821 | intron-variant | HDAC4 | GRCh38.p7 | 2:239143926 | GGTGCTGTGATTTCA[C/G]GAGTGGTGGGGTGAG | 9759 |
rs3791480 | snp | A/G | 0.42803 | 0.175514 | intron-variant | HDAC4 | GRCh38.p7 | 2:239144037 | GATGGGGGTCTGCTC[A/G]GTCTTGTCCTTCTGC | 9759 |
rs3791481 | snp | C/T | 0.427727 | 0.175821 | intron-variant | HDAC4 | GRCh38.p7 | 2:239144223 | GAACAGGGCAGAGCA[C/T]GCGATTCACCACTAC | 9759 |
rs3791482 | snp | A/G | 0.135825 | 0.222405 | intron-variant | HDAC4 | GRCh38.p7 | 2:239145174 | CTGACAGGGATGTGA[A/G]GCTGGGCCCAGGGAT | 9759 |
rs3791483 | snp | A/G | 0.35574 | 0.226537 | intron-variant | HDAC4 | GRCh38.p7 | 2:239145312 | CTGGGGAGGCTCAGC[A/G]GAGCCCATCCCAACA | 9759 |
rs3791484 | snp | A/G | 0.325563 | 0.238307 | intron-variant | HDAC4 | GRCh38.p7 | 2:239145533 | GGATCTAAAGGCAGC[A/G]ACCGGAGTCAAAGAA | 9759 |
rs3791485 | snp | C/T | 0.433527 | 0.169758 | intron-variant | HDAC4 | GRCh38.p7 | 2:239145535 | ATCTAAAGGCAGCGA[C/T]CGGAGTCAAAGAAAT | 9759 |
rs3791486 | snp | A/G | 0.316968 | 0.240864 | intron-variant | HDAC4 | GRCh38.p7 | 2:239146008 | GAGAGGCGCTGTGAG[A/G]AGGTACCAGACTCTA | 9759 |
rs3791487 | snp | C/G | 0.199873 | 0.244923 | intron-variant | HDAC4 | GRCh38.p7 | 2:239146126 | CCACGGGCTACTGAC[C/G]AGGGCACACTTCTGT | 9759 |
rs3791489 | snp | A/G | 0.159622 | 0.233092 | intron-variant | HDAC4 | GRCh38.p7 | 2:239147362 | ATTGACTTAAGACAT[A/G]GGGACCTACAATATC | 9759 |
rs3791493 | snp | A/T | 0.379522 | 0.213832 | intron-variant | HDAC4 | GRCh38.p7 | 2:239149397 | AAATAAATAAATAAA[A/T]AAAAAGATAATTCTA | 9759 |
rs3791494 | snp | A/G | 0.159951 | 0.233219 | intron-variant | HDAC4 | GRCh38.p7 | 2:239151101 | CCAAACTCAGGGATG[A/G]ATGTGAGGGTGGAAA | 9759 |
rs3791495 | snp | C/T | 0.15698 | 0.23205 | intron-variant | HDAC4 | GRCh38.p7 | 2:239151407 | ACCAAGCGGGACAGC[C/T]TCCCCCCAAAATGGA | 9759 |
rs3791496 | snp | A/G | 0.15698 | 0.23205 | intron-variant | HDAC4 | GRCh38.p7 | 2:239152031 | TCTATCAGCAGTCAC[A/G]TGAGGGGAAAATTTA | 9759 |
rs3791497 | snp | G/T | 0.162253 | 0.234095 | intron-variant | HDAC4 | GRCh38.p7 | 2:239152549 | GGCCCTGGGTAGAGG[G/T]CTCTGACTCTCAAGC | 9759 |
rs3791498 | snp | A/G | 0.486855 | 0.0799975 | intron-variant | HDAC4 | GRCh38.p7 | 2:239153339 | ATAAGTTAATGTAAA[A/G]TCAAAATCATATAAT | 9759 |
rs3791499 | snp | A/G | 0.332568 | 0.235971 | intron-variant | HDAC4 | GRCh38.p7 | 2:239153567 | TTAAGTGGTTTAAAC[A/G]TTTTCTCGGAAATCT | 9759 |
rs3791500 | snp | C/T | 0.494057 | 0.0541878 | intron-variant | HDAC4 | GRCh38.p7 | 2:239153849 | GGAAGCCAACAGCCA[C/T]GGAATCTACGAGAGA | 9759 |
rs3791501 | snp | C/T | 0.499741 | 0.0113788 | intron-variant | HDAC4 | GRCh38.p7 | 2:239153894 | CCTATGGGAGAAAGG[C/T]CTCTGATGGTGAACA | 9759 |
rs3791502 | snp | C/T | 0.159951 | 0.233219 | intron-variant | HDAC4 | GRCh38.p7 | 2:239153935 | GCCGTGACAGTGTGC[C/T]GTCTCCCATGCTGAT | 9759 |
rs3791503 | snp | A/G | 0.440333 | 0.16209 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239155016 | CCACCAGCCCGATAC[A/G]GCCCACTCCTCTGAG | 9759 |
rs3791504 | snp | C/T | 0.499879 | 0.0077866 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239155675 | TTGTGTGACTGAGTA[C/T]GTTCACTGTTTCCGC | 9759 |
rs3791505 | snp | C/T | 0.333722 | 0.235565 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239155777 | ATCTCCAAGAGCCGC[C/T]CCCTAGGGAGGACGC | 9759 |
rs3791506 | snp | A/G | 0.499902 | 0.00698814 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239155791 | CCCCCTAGGGAGGAC[A/G]CCTTGGGATTTCCCA | 9759 |
rs3791507 | snp | A/G | 0.207253 | 0.246318 | intron-variant | HDAC4 | GRCh38.p7 | 2:239157209 | ATAGGCAGCTGAGAC[A/G]GGGCAAAAAACGGTC | 9759 |
rs3791508 | snp | C/G | 0.499933 | 0.00579035 | intron-variant | HDAC4 | GRCh38.p7 | 2:239158051 | GCAGTCAGGCTCGGA[C/G]TGCAGGGCTGGGACA | 9759 |
rs3791509 | snp | A/G | 0.32955 | 0.237006 | intron-variant | HDAC4 | GRCh38.p7 | 2:239158603 | GGGCCCTGCCCCCCA[A/G]CTGCCAGCGCCTCCC | 9759 |
rs3791510 | snp | C/T | 0.165527 | 0.235296 | intron-variant | HDAC4 | GRCh38.p7 | 2:239158782 | AGGGCAGGTCACACC[C/T]GCCCAGCCCTGGTCA | 9759 |
rs3791511 | snp | A/G | 0.157972 | 0.232445 | intron-variant | HDAC4 | GRCh38.p7 | 2:239158844 | CCTCCGCGAAGAAGC[A/G]TCCAGCAGGGCGAGC | 9759 |
rs3791512 | snp | C/G | 0.339882 | 0.233284 | intron-variant | HDAC4 | GRCh38.p7 | 2:239159844 | CCTGGGGATGGGACA[C/G]AGACGCTGGGCCAGG | 9759 |
rs3791513 | snp | C/T | 0.16028 | 0.233346 | intron-variant | HDAC4 | GRCh38.p7 | 2:239159851 | ATGGGACACAGACGC[C/T]GGGCCAGGAGCCGAG | 9759 |
rs3791514 | snp | A/G | 0.436408 | 0.16659 | intron-variant | HDAC4 | GRCh38.p7 | 2:239159906 | GCCAACCCGGATGCC[A/G]CACCTAAAGGCAAAC | 9759 |
rs3791515 | snp | A/G | 0.425863 | 0.177686 | intron-variant | HDAC4 | GRCh38.p7 | 2:239161832 | CACCCCTCCTCCCTG[A/G]AAGCCCCCCATCTCC | 9759 |
rs3791516 | snp | A/T | 0.10829 | 0.205957 | intron-variant | HDAC4 | GRCh38.p7 | 2:239162357 | GCCCCTGGCTCCTCA[A/T]CCTGCCCTTTCCAGC | 9759 |
rs3791517 | snp | C/G | 0.49928 | 0.018956 | intron-variant | HDAC4 | GRCh38.p7 | 2:239162605 | CTCAGGTCCCAGTGG[C/G]TCACTGCTGTCACGT | 9759 |
rs3791518 | snp | A/G | 0.161267 | 0.233723 | intron-variant | HDAC4 | GRCh38.p7 | 2:239162697 | TACCCAAATCCAGAC[A/G]GTGTGTCTGCCGTGA | 9759 |
rs3791519 | snp | C/T | 0.154661 | 0.231107 | intron-variant | HDAC4 | GRCh38.p7 | 2:239165575 | CTAGTATATGCCAGC[C/T]CTGGCCTGGTTCGGC | 9759 |
rs3791520 | snp | A/G | 0.261332 | 0.249743 | intron-variant | HDAC4 | GRCh38.p7 | 2:239165948 | ATTTGGTTATTTGCT[A/G]AATTTTTTCATGACT | 9759 |
rs3791521 | snp | A/G | 0.49941 | 0.0171624 | intron-variant | HDAC4 | GRCh38.p7 | 2:239166307 | ACTACACGACCACCA[A/G]CATGAGTCCGGGAAG | 9759 |
rs3791522 | snp | C/T | 0.499382 | 0.017561 | intron-variant | HDAC4 | GRCh38.p7 | 2:239166412 | AAGCTGTGCCTGTGA[C/T]GTCCCCCAGCTCATG | 9759 |
rs3791523 | snp | A/G | 0.338523 | 0.233803 | intron-variant | HDAC4 | GRCh38.p7 | 2:239166779 | ATAAAAGGAAAGGCC[A/G]GGCGGTGGGGAAGAT | 9759 |
rs3791524 | snp | C/T | 0.236724 | 0.249647 | intron-variant | HDAC4 | GRCh38.p7 | 2:239167077 | GCAGGTCCCCCTACA[C/T]GGCCGTCCTTGAGTG | 9759 |
rs3791526 | snp | C/T | 0.154993 | 0.231244 | intron-variant | HDAC4 | GRCh38.p7 | 2:239169628 | AAGAACACTGCCAGC[C/T]GGGTTCCACTTGGGA | 9759 |
rs3791527 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | HDAC4 | GRCh38.p7 | 2:239169815 | CTCTCCCCTATGCCG[C/T]CCCGTCTCCTCAAGG | 9759 |
rs3791529 | snp | A/G | 0.389715 | 0.207315 | intron-variant | HDAC4 | GRCh38.p7 | 2:239170827 | TCAACAGTGGGTTTC[A/G]GAAGAGGCCCTTGAT | 9759 |
rs3791531 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | HDAC4 | GRCh38.p7 | 2:239170916 | TAGGACCTCAAAGGG[A/T]TATGCCTTATGAGTA | 9759 |
rs3791533 | snp | A/G | 0.367503 | 0.220665 | intron-variant | HDAC4 | GRCh38.p7 | 2:239178920 | CAAAGCATAGAGTGG[A/G]GTGTGTGTGCGAGGC | 9759 |
rs3791536 | snp | A/G | 0.342582 | 0.232225 | intron-variant | HDAC4 | GRCh38.p7 | 2:239180017 | CCCTTCTCTGTGGGC[A/G]CCAACCTTCAGCGGC | 9759 |
rs3791538 | snp | C/T | 0.148996 | 0.228688 | intron-variant | HDAC4 | GRCh38.p7 | 2:239180314 | TTTCATGGTCACAGG[C/T]GGTGCAGGGGATGAG | 9759 |
rs3791539 | snp | C/T | 0.348134 | 0.229934 | intron-variant | HDAC4 | GRCh38.p7 | 2:239180631 | AGCCCAGACAAGGGA[C/T]AGAGACAGGCATTGG | 9759 |
rs3791540 | snp | A/G | 0.126564 | 0.217402 | intron-variant | HDAC4 | GRCh38.p7 | 2:239181145 | CCGGCTCTCCTCACA[A/G]ATGAAAAGCCCTGTC | 9759 |
rs3791542 | snp | C/T | 0.285519 | 0.247464 | intron-variant | HDAC4 | GRCh38.p7 | 2:239182259 | AACTGATCTCCTCGT[C/T]ATGGCGAGCCCCTCC | 9759 |
rs3791543 | snp | C/T | 0.149999 | 0.229128 | intron-variant | HDAC4 | GRCh38.p7 | 2:239182271 | CGTCATGGCGAGCCC[C/T]TCCCCTCTGGCTGTC | 9759 |
rs3791549 | snp | A/G | 0.342358 | 0.232314 | intron-variant | HDAC4 | GRCh38.p7 | 2:239187328 | CAACATGCAGAATAC[A/G]AAGGAGCTACGGTAC | 9759 |
rs3791551 | snp | A/G | 0.426354 | 0.177198 | intron-variant | HDAC4 | GRCh38.p7 | 2:239187585 | GGCCAGAAAAACAGA[A/G]GCCAGCTGCAGTTGC | 9759 |
rs3791552 | snp | A/T | 0.146314 | 0.227484 | intron-variant | HDAC4 | GRCh38.p7 | 2:239187779 | CACCCTAAACTCGAG[A/T]GTGCTTGTTAAAGTG | 9759 |
rs3791553 | snp | C/T | 0.425586 | 0.17796 | intron-variant | HDAC4 | GRCh38.p7 | 2:239187781 | CCCTAAACTCGAGTG[C/T]GCTTGTTAAAGTGGA | 9759 |
rs3791554 | snp | A/G | 0.239902 | 0.249796 | intron-variant | HDAC4 | GRCh38.p7 | 2:239190318 | GCCCATGGGAGGTCA[A/G]GCCAGGACGCACTCC | 9759 |
rs3791556 | snp | A/G | 0.314544 | 0.241524 | intron-variant | HDAC4 | GRCh38.p7 | 2:239191276 | AGCACCTTTGGGCGT[A/G]ACCTTGTCCAGGTGC | 9759 |
rs3791558 | snp | A/G | 0.309154 | 0.242901 | intron-variant | HDAC4 | GRCh38.p7 | 2:239191559 | TCAGCCTTCTCCTGA[A/G]AAAAGGGTGGGAAAT | 9759 |
rs3791562 | snp | C/T | 0.316 | 0.241131 | intron-variant | HDAC4 | GRCh38.p7 | 2:239191740 | CCTCCCCTGCCCCAC[C/T]GCAGTCAATCATGCT | 9759 |
rs3791563 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | HDAC4 | GRCh38.p7 | 2:239192114 | ATGTGAGAAGAATCT[A/G]CGCACATAAACTGCG | 9759 |
rs3791566 | snp | C/T | 0.146314 | 0.227484 | intron-variant | HDAC4 | GRCh38.p7 | 2:239192620 | CTCTCACAAGCACGG[C/T]GGTGCTAAATGCTTT | 9759 |
rs3791568 | snp | A/G | 0.31014 | 0.242659 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194005 | CCTGGCCAGATCTGA[A/G]CCCGGGGTGGTCAAT | 9759 |
rs3791570 | snp | C/T | 0.077417 | 0.180873 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194602 | CCCAGCACTCCCCAC[C/T]CCCAAAAGACAGGAC | 9759 |
rs3791571 | snp | G/T | 0.077417 | 0.180873 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194746 | TGGGAAGCTGCTTCC[G/T]ACTCCTCCAGGCCCC | 9759 |
rs3791572 | snp | C/T | 0.078151 | 0.181571 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194949 | TCTGTGTCTCCAGCT[C/T]GGTGCGCGTCTCCCT | 9759 |
rs3791573 | snp | A/G | | | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194950 | CTGTGTCTCCAGCTC[A/G]GTGCGCGTCTCCCTA | 9759 |
rs3791574 | snp | C/G | 0.0777841 | 0.181223 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194961 | GCTCGGTGCGCGTCT[C/G]CCTACGGACATGGAA | 9759 |
rs3791575 | snp | C/T | 0.389903 | 0.207189 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194966 | GTGCGCGTCTCCCTA[C/T]GGACATGGAAGAGTG | 9759 |
rs3791576 | snp | A/G | 0.079617 | 0.182947 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239195162 | TACGGCACCTCCTGC[A/G]TTTTCACTCATTGTG | 9759 |
rs3791577 | snp | A/C/T | 0.0150663 | 0.0855261 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239195219 | TTTACCGGACTGCCA[A/C/T]GTGAAACTCCACTAT | 9759 |
rs3791578 | snp | A/G | 0.081446 | 0.184634 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239195363 | TTTATGTTGGATTCA[A/G]TAACACAAATGGAGC | 9759 |
rs3791580 | snp | G/T | 0.301429 | 0.244653 | intron-variant | HDAC4 | GRCh38.p7 | 2:239198820 | AAATACACAAAAGCA[G/T]GAAGAATAGTGTAAT | 9759 |
rs3791581 | snp | A/G | 0.328382 | 0.237395 | intron-variant | HDAC4 | GRCh38.p7 | 2:239199052 | TCACGATCCAAATAC[A/G]TTGTAATTAGCTGAT | 9759 |
rs3791585 | snp | C/T | 0.231482 | 0.249313 | intron-variant | HDAC4 | GRCh38.p7 | 2:239200851 | GGCAGCTGCAGCACA[C/T]GGCCAGGCCTGGATG | 9759 |
rs3791588 | snp | A/C | 0.2768 | 0.248559 | intron-variant | HDAC4 | GRCh38.p7 | 2:239202010 | CCTGCAGTTGGCAGG[A/C]TCTTTCCCCAGCCTC | 9759 |
rs3791590 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HDAC4 | GRCh38.p7 | 2:239203535 | GAGTCCTGTGGTCTC[A/G]AAGCTGAACCGCTTT | 9759 |
rs3791591 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | HDAC4 | GRCh38.p7 | 2:239204528 | TCGGATCACGTCCAG[C/T]GAAACCGGCCCTTAC | 9759 |
rs3791592 | snp | C/T | 0.00558427 | 0.0525448 | intron-variant | HDAC4 | GRCh38.p7 | 2:239204612 | AGGGAAAAGAGGGTC[C/T]GTGGAGGGCTGCACC | 9759 |
rs3791594 | snp | A/C | 0.0916144 | 0.193427 | intron-variant | HDAC4 | GRCh38.p7 | 2:239205853 | TTAAAGTGTCTGTAA[A/C]CCACGTGTTGTAGAG | 9759 |
rs3791596 | snp | C/G | 0.274929 | 0.248754 | intron-variant | HDAC4 | GRCh38.p7 | 2:239209660 | ATGACGTTGTTACAT[C/G]TGACTACATTTAAAT | 9759 |
rs3791597 | snp | C/G | 0.406468 | 0.194981 | intron-variant | HDAC4 | GRCh38.p7 | 2:239210525 | TGAATGGCTTTACTA[C/G]AAACGTGTACATTTA | 9759 |
rs3791598 | snp | C/T | 0.274393 | 0.248807 | intron-variant | HDAC4 | GRCh38.p7 | 2:239210562 | GGCCTGTGAGCACAA[C/T]GGCTTGGGGCTCCCT | 9759 |
rs3791599 | snp | C/T | 0.274124 | 0.248833 | intron-variant | HDAC4 | GRCh38.p7 | 2:239210972 | AACACACTCCACAAA[C/T]ACTGAGGGTCCTTTA | 9759 |
rs3791600 | snp | A/G | 0.211819 | 0.247067 | intron-variant | HDAC4 | GRCh38.p7 | 2:239211285 | TGTTGCCCTCACAAT[A/G]CAAAATCACTAAGCA | 9759 |
rs3791601 | snp | C/T | 0.174288 | 0.23826 | intron-variant | HDAC4 | GRCh38.p7 | 2:239212014 | CACAGGGTCACTTTT[C/T]AGAAAACATCCCTTA | 9759 |
rs3791603 | snp | A/G | 0.212122 | 0.247114 | intron-variant | HDAC4 | GRCh38.p7 | 2:239212357 | CTAGGGCACTGACCC[A/G]ACTCCCTCAACCCCA | 9759 |
rs3791604 | snp | A/C | 0.0908922 | 0.192833 | intron-variant | HDAC4 | GRCh38.p7 | 2:239212603 | CCATACAGGGACCAA[A/C]CCCATTCCCCCAGAA | 9759 |
rs3791605 | snp | C/G | 0.0908922 | 0.192833 | intron-variant | HDAC4 | GRCh38.p7 | 2:239212704 | GCTGACATGCCAAGG[C/G]GTGAGGCTGTGTGAG | 9759 |
rs3791607 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | HDAC4 | GRCh38.p7 | 2:239213556 | CTATCCCCAAAAGCC[C/T]GCATCTGCATAGTCA | 9759 |
rs3791608 | snp | A/G | 0.305186 | 0.243833 | intron-variant | HDAC4 | GRCh38.p7 | 2:239216751 | GGAACAGGACTGACC[A/G]GGAAGGGTGTGTGTC | 9759 |
rs3791610 | snp | C/T | 0.499776 | 0.0105807 | intron-variant | HDAC4 | GRCh38.p7 | 2:239222176 | CCGTGATGTTATTCT[C/T]GTGGAATTCCGTGTG | 9759 |
rs3791611 | snp | A/C/T | 0.0103295 | 0.0711199 | intron-variant | HDAC4 | GRCh38.p7 | 2:239222533 | AGGCCTTACCCCATA[A/C/T]CAAAAAAAAAAAAAA | 9759 |
rs3791612 | snp | A/T | 0.230896 | 0.249269 | intron-variant | HDAC4 | GRCh38.p7 | 2:239223512 | CACCTGGGCAGCTTG[A/T]TAAAAAGTGACTTAC | 9759 |
rs3791615 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239225595 | GGGAAGCCAGGAAGG[C/T]GGGGAAGGCAGGTCG | 9759 |
rs3791616 | snp | A/G | 0.31357 | 0.241783 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239226836 | TCCTGGGCCGCGTGG[A/G]GAGGCACGGTCCCAC | 9759 |
rs3791617 | snp | A/G | 0.0399052 | 0.1355 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239227105 | GCCAGGGTGGGCCAA[A/G]GGAGGGGCAGACCAG | 9759 |
rs3791618 | snp | C/G | 0.231482 | 0.249313 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239227160 | CACAGGGGCTGGTGG[C/G]ACCAGGACTGGAGGT | 9759 |
rs3791623 | snp | A/C | 0.410737 | 0.191478 | intron-variant | HDAC4 | GRCh38.p7 | 2:239233966 | TGAGGACTGACATAA[A/C]ATATACCTAAAAATG | 9759 |
rs3791624 | snp | C/T | 0.354881 | 0.226936 | intron-variant | HDAC4 | GRCh38.p7 | 2:239234244 | TGGGCATCGCTGCTA[C/T]GTTATTTAAAATTAC | 9759 |
rs3791625 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | HDAC4 | GRCh38.p7 | 2:239234678 | AGCAACTCGCCTAAG[C/T]TCCCACGCAAACAGG | 9759 |
rs3811563 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239052272 | CGCGAGCTGGCCTGA[C/T]GCCTCAAGCACGGGC | 9759 |
rs3811564 | snp | C/T | 0.124491 | 0.216211 | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239048916 | AGAACTGGGCGGACT[C/T]GAAAGAGTCCCCTTT | 9759 |
rs3816376 | snp | A/G | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239080587 | GCAGGGCGCCGTTTA[A/G]AGACGCAGTGTTTGC | 9759 |
rs3816377 | snp | A/C/T | 0.000710586 | 0.0188377 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239156609 | GGCGTGGAAGGTGCC[A/C/T]GTGCAGGAGACCTCC | 9759 |
rs3828195 | snp | A/G | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | HDAC4, MIR4441 | GRCh38.p7 | 2:239087905 | AACTGTCGGTGAGGC[A/G]TGGTGCCCTTGGCTC | 9759 |
rs3828196 | snp | A/G | 0.283158 | 0.247791 | intron-variant | HDAC4 | GRCh38.p7 | 2:239095628 | GAGGGCTCCAAGGAC[A/G]CTGCAGCTGCACGCC | 9759 |
rs3828197 | snp | A/G | 0.36955 | 0.219562 | intron-variant | HDAC4 | GRCh38.p7 | 2:239097414 | ATGGCTCACGGACCC[A/G]CCACTGCCTGGAGTC | 9759 |
rs3828198 | snp | C/T | 0.367708 | 0.220556 | intron-variant | HDAC4 | GRCh38.p7 | 2:239098332 | TACTTGTCTGTTTGC[C/T]GCGGGCTGGCAGACA | 9759 |
rs3828199 | snp | C/T | 0.368938 | 0.219895 | intron-variant | HDAC4 | GRCh38.p7 | 2:239098334 | CTTGTCTGTTTGCCG[C/T]GGGCTGGCAGACAGG | 9759 |
rs3828200 | snp | A/G | 0.352721 | 0.227922 | intron-variant | HDAC4 | GRCh38.p7 | 2:239098335 | TTGTCTGTTTGCCGC[A/G]GGCTGGCAGACAGGC | 9759 |
rs3828201 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HDAC4 | GRCh38.p7 | 2:239103638 | GGTTGTGGCTGTTAC[C/T]TGCTTCCCCCAGGCC | 9759 |
rs3828202 | snp | A/G | 0.490943 | 0.0666801 | intron-variant | HDAC4 | GRCh38.p7 | 2:239108426 | CTCATGCTCACAGTA[A/G]CGCCCCAGGACCCAG | 9759 |
rs3828203 | snp | C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239108852 | CAGCATGGACGGGCC[C/T]CCAGGGTGCGGCAGC | 9759 |
rs3828204 | snp | A/G | 0.172674 | 0.237741 | intron-variant | HDAC4 | GRCh38.p7 | 2:239109293 | CAGGCTGATAAGGGC[A/G]GGGCGCACGGTGAAG | 9759 |
rs3828205 | snp | C/T | 0.499974 | 0.00359416 | intron-variant | HDAC4 | GRCh38.p7 | 2:239121350 | TGGCGGTGGAGGTAG[C/T]GGGGGTCATAGCGGG | 9759 |
rs3828206 | snp | A/G | 0.31357 | 0.241783 | intron-variant | HDAC4 | GRCh38.p7 | 2:239126809 | CCCGCCAGCCCAGGC[A/G]TTCTGCCCTGGTGCC | 9759 |
rs3828207 | snp | G/T | 0.148996 | 0.228688 | intron-variant | HDAC4 | GRCh38.p7 | 2:239127696 | GAGGCCCTGGTGGGG[G/T]ACTCTTTGGAACTCG | 9759 |
rs3828208 | snp | G/T | 0.429987 | 0.173507 | intron-variant | HDAC4 | GRCh38.p7 | 2:239142106 | AAGGCACAGAACACG[G/T]GCTGCGGGAATGTGC | 9759 |
rs3828209 | snp | C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239142573 | CTAGGTGCCTCGGCA[C/T]GGGCTCCCTTTATGC | 9759 |
rs3828210 | snp | C/T | 0.418974 | 0.184249 | intron-variant | HDAC4 | GRCh38.p7 | 2:239143835 | CCTTGGCCTTCAAGT[C/T]GAACACTTTCTGTTG | 9759 |
rs3828211 | snp | C/G | 0.427575 | 0.175975 | intron-variant | HDAC4 | GRCh38.p7 | 2:239144337 | CACCCTTGTGCACCT[C/G]AGCCCACCTAGAACC | 9759 |
rs3828213 | snp | A/G | 0.257454 | 0.249889 | intron-variant | HDAC4 | GRCh38.p7 | 2:239149549 | GAACGCACTGCCGCT[A/G]AGCAACCTCCATTCA | 9759 |
rs3828214 | snp | A/G | 0.351418 | 0.228505 | intron-variant | HDAC4 | GRCh38.p7 | 2:239149551 | ACGCACTGCCGCTAA[A/G]CAACCTCCATTCAGC | 9759 |
rs3828215 | snp | A/C | 0.15698 | 0.23205 | intron-variant | HDAC4 | GRCh38.p7 | 2:239151410 | AAGCGGGACAGCTTC[A/C]CCCCAAAATGGAGGA | 9759 |
rs3828216 | snp | C/T | 0.499846 | 0.00878459 | intron-variant | HDAC4 | GRCh38.p7 | 2:239162035 | CCACTGACTCCTGGG[C/T]GAGGGGGCGCCAGCT | 9759 |
rs3828217 | snp | C/T | 0.164546 | 0.234942 | intron-variant | HDAC4 | GRCh38.p7 | 2:239162555 | CGGGCTCCCAGGTGC[C/T]GGTTGCCAGCGATTC | 9759 |
rs3828218 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | HDAC4 | GRCh38.p7 | 2:239163048 | TCACTGTTTCAAGCC[G/T]CATCACCTCGCCACT | 9759 |
rs3828219 | snp | C/T | 0.499354 | 0.0179596 | intron-variant | HDAC4 | GRCh38.p7 | 2:239164720 | GGTCAAAAACACACC[C/T]TGAGGTGAGTGAAGC | 9759 |
rs3828220 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | HDAC4 | GRCh38.p7 | 2:239181441 | CACGCCCGGCAGCAG[C/T]GTGTGCGCAGGAGGG | 9759 |
rs3828222 | snp | C/T | 0.341685 | 0.232581 | intron-variant | HDAC4 | GRCh38.p7 | 2:239187872 | ACACGGCTGCTAGGT[C/T]GCTCTGAAATCTGAA | 9759 |
rs3828223 | snp | C/T | 0.146314 | 0.227484 | intron-variant | HDAC4 | GRCh38.p7 | 2:239188353 | ACAAAGTGTCTTACA[C/T]ATAAAGGAAGGGAAA | 9759 |
rs3828224 | snp | C/T | | | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239193678 | GAGAGCAGCCAAGAG[C/T]GCGAGGGGAAGCAGC | 9759 |
rs3828225 | snp | A/C | 0.225005 | 0.248747 | intron-variant | HDAC4 | GRCh38.p7 | 2:239202033 | CCAGCCTCCACCCCC[A/C]TGCAGGCATCTCCAG | 9759 |
rs3828227 | snp | A/T | 0.274661 | 0.248781 | intron-variant | HDAC4 | GRCh38.p7 | 2:239206330 | AAAAACCTGCCTCAA[A/T]AAAAAAGAAAGTAAT | 9759 |
rs3828231 | snp | A/G | 0.355954 | 0.226437 | intron-variant | HDAC4 | GRCh38.p7 | 2:239234704 | ACAGGCAGCAGAGGC[A/G]GGCCCCAGGTGCCCT | 9759 |
rs3834782 | in-del | -/C | 0.077417 | 0.180873 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239193514 | CCCAGGGGAAGGGCC[-/C]ACAGTGGGCTGCGTC | 9759 |
rs3838507 | in-del | -/G | 0.473359 | 0.112298 | intron-variant | HDAC4 | GRCh38.p7 | 2:239078404 | GCATGCATTGTCCCC[-/G]GGGGGCCCCCGTGGG | 9759 |
rs3838508 | in-del | -/CACA | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239079845 | ACACAGCGATATACA[-/CACA]AAGACATGTGCATGC | 9759 |
rs3838509 | in-del | -/G | 0.39527 | 0.203462 | intron-variant | HDAC4 | GRCh38.p7 | 2:239106742 | CCAGCTTCTAAAGGA[-/G]GGGCAGGCGAACCTG | 9759 |
rs3838510 | in-del | -/TTCT | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239118225 | ATCCCTTAACTTTCT[-/TTCT]AAGAGCAGTTTAAAG | 9759 |
rs3838511 | in-del | -/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239141855 | TAATTTTATTTTTTT[-/T]GCATTCTACTTCCAG | 9759 |
rs3838512 | in-del | -/A | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239143260 | ACTTTAAAAAAAAAA[-/A]CAACAAAAAAACGCA | 9759 |
rs3838513 | in-del | -/AACAGCTCTGCCTGTG | 0.375 | 0.216506 | intron-variant | HDAC4 | GRCh38.p7 | 2:239145394 | GGGTCGGTTTCTGTG[-/AACAGCTCTGCCTGTG]TGGACAGAGCCATTT | 9759 |
rs3838514 | in-del | -/AG | 0.5 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239145802 | CAAGGAATGAGACGG[-/AG]TTTCTCCTGGAAGCA | 9759 |
rs3838515 | in-del | -/TAAA | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239149400 | AAATAAATAAATAAA[-/TAAA]AAGATAATTCTAAAA | 9759 |
rs3838516 | in-del | -/A | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239151995 | GGACAACAGTTAGTT[-/A]GTTGTTTTGGCCTCC | 9759 |
rs3838517 | in-del | -/AGTG | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239187195 | CGGAGTGAGTGAGTG[-/AGTG]GTCCTCATGTCCCCG | 9759 |
rs3838519 | in-del | -/CACACACA | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239221639 | ACACACACACACACA[-/CACACACA]GCCTTCAACTGAAGA | 9759 |
rs3841081 | in-del | -/CTAT/CTATCTAT/CTATCTATCTAT/CTATCTATCTATCTAT | 0.32708 | 0.271616 | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239048560 | tatctatctatctat[lengthTooLong]ACAGGGGGCTTGAAC | 9759 |
rs3842553 | in-del | -/CGGCCTCCCTCCCTCTGCC | 0 | 0 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239176389 | CTCCCTCCCTCTGCC[-/CGGCCTCCCTCCCTCTGCC]TGGCCTTCCGTGCCC | 9759 |
rs3842554 | in-del | -/AGAAAATCAAAGATCCTT | 0.483053 | 0.0904792 | intron-variant | HDAC4 | GRCh38.p7 | 2:239236833 | ATTTGTATTTGCCAA[-/AGAAAATCAAAGATCCTT]TGTAGAATAATCAAA | 9759 |
rs4132982 | snp | C/T | | | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239313811 | GTTTC[C/T] | 9759 |
rs4456728 | snp | A/T | 0.339429 | 0.233457 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239225926 | AAAAGATGGGCAGGT[A/T]CCTCTGGTAGGGGAC | 9759 |
rs4482505 | snp | C/G | 0.423413 | 0.180077 | intron-variant | HDAC4 | GRCh38.p7 | 2:239373091 | GTCCTGGGGTCTGTG[C/G]CCCTGTGGAGCACAG | 9759 |
rs4490210 | snp | C/T | 0.448323 | 0.15221 | intron-variant | HDAC4 | GRCh38.p7 | 2:239263171 | TGTCTGCTGTGTCGG[C/T]GCCCTAGCCTCTGCC | 9759 |
rs4502439 | snp | A/G | 0.333261 | 0.235728 | intron-variant | HDAC4 | GRCh38.p7 | 2:239293067 | AGGTGTGAGGCCAGC[A/G]GCCAGCTCCCAGGTA | 9759 |
rs4507124 | snp | A/G | 0.160938 | 0.233598 | intron-variant | HDAC4 | GRCh38.p7 | 2:239132409 | CAACCTGGGGAGGCT[A/G]TGCAGGAGAGAAGGG | 9759 |
rs4572614 | snp | A/G | 0.321292 | 0.23962 | intron-variant | HDAC4 | GRCh38.p7 | 2:239132510 | AGAGCAAGCTGGGCA[A/G]CCATGCATGGGCCCC | 9759 |
rs4622755 | snp | A/G | 0.40853 | 0.193309 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239226050 | ACAAGGGTCGGCAAA[A/G]AGCCATCTCCCTCGT | 9759 |
rs4629183 | snp | A/C | 0.202343 | 0.245416 | intron-variant | HDAC4 | GRCh38.p7 | 2:239132354 | ACGTGACACTGGCTC[A/C]GAGGCTCCCTGCCAG | 9759 |
rs4629184 | snp | C/T | 0.20511 | 0.245937 | intron-variant | HDAC4 | GRCh38.p7 | 2:239132408 | GCAACCTGGGGAGGC[C/T]GTGCAGGAGAGAAGG | 9759 |
rs4851967 | snp | C/T | 0.301932 | 0.244547 | intron-variant | HDAC4 | GRCh38.p7 | 2:239068148 | CGCCTGCCAGAGAAG[C/T]GGCATGGGGCACATC | 9759 |
rs4851968 | snp | A/G | 0.133777 | 0.221342 | intron-variant | HDAC4 | GRCh38.p7 | 2:239104395 | CATCACACCTGGCTA[A/G]TTTTTGTATTTTTAT | 9759 |
rs4851969 | snp | C/G | 0.363985 | 0.222503 | intron-variant | HDAC4 | GRCh38.p7 | 2:239302072 | CATGGAAAATAATCT[C/G]TAATGATGCTATAAA | 9759 |
rs4851970 | snp | C/T | 0.324382 | 0.238678 | intron-variant | HDAC4 | GRCh38.p7 | 2:239317739 | AGTCCACATTTCACG[C/T]TGTCCACAGGTTCTT | 9759 |
rs4851971 | snp | C/T | 0.441977 | 0.16014 | intron-variant | HDAC4 | GRCh38.p7 | 2:239318510 | GAGACATCACTAGAC[C/T]ATCAGCGAAACATAA | 9759 |
rs4851972 | snp | A/G | 0.324145 | 0.238752 | intron-variant | HDAC4 | GRCh38.p7 | 2:239327224 | CCTGGGAGCCTAGCC[A/G]TACCCACCTGGGAGG | 9759 |
rs4851973 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | HDAC4 | GRCh38.p7 | 2:239332127 | tgacagagctaaaaa[C/G]agaaacaatgccaat | 9759 |
rs4852010 | snp | C/T | 0.446249 | 0.154875 | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239051187 | CACGGAGGGGAAAAA[C/T]ACACCACCCCTCGTA | 9759 |
rs4852013 | snp | A/G | 0.316726 | 0.240931 | intron-variant | HDAC4 | GRCh38.p7 | 2:239061654 | AGTGACTGGAAGCAG[A/G]CAGCCAGCTCTCAGG | 9759 |
rs4852017 | snp | C/T | 0.456095 | 0.141508 | intron-variant, upstream-variant-2KB | HDAC4, MIR4441 | GRCh38.p7 | 2:239086494 | TCTCTTCCCTGCACA[C/T]GAAGGAGACTCTGCT | 9759 |
rs4852018 | snp | A/G | 0.492823 | 0.0594727 | intron-variant | HDAC4 | GRCh38.p7 | 2:239093078 | GTACGAGAGCAGGCC[A/G]GGACTCCGCTGGGCG | 9759 |
rs4852019 | snp | A/G | 0.493613 | 0.0561475 | intron-variant | HDAC4 | GRCh38.p7 | 2:239098926 | CAGATTTTAAAGCAC[A/G]AAGCTTTCCAGGAAA | 9759 |
rs4852020 | snp | G/T | 0.369142 | 0.219784 | intron-variant | HDAC4 | GRCh38.p7 | 2:239099021 | GGAGAACAGGAATGG[G/T]GCAAAGGGATGCTGC | 9759 |
rs4852021 | snp | C/T | 0.427119 | 0.176434 | intron-variant | HDAC4 | GRCh38.p7 | 2:239111989 | GGATCCTGCCATGGG[C/T]TACGTTAACAGGATA | 9759 |
rs4852022 | snp | C/T | 0.16911 | 0.236552 | intron-variant | HDAC4 | GRCh38.p7 | 2:239125346 | tcttgccaagtgatg[C/T]gcccgctcccccttc | 9759 |
rs4852023 | snp | A/G | 0.183886 | 0.241099 | intron-variant | HDAC4 | GRCh38.p7 | 2:239128386 | ATACAAAAATCAGCC[A/G]TGTATGGTGGCACAT | 9759 |
rs4852024 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | HDAC4 | GRCh38.p7 | 2:239134089 | TTTCACTGCAGTCAC[A/G]GTGGCTACATCACGT | 9759 |
rs4852025 | snp | C/T | 0.32 | 0.24 | intron-variant | HDAC4 | GRCh38.p7 | 2:239150580 | TATATACCACACCTT[C/T]ACATACAGCAGCAGG | 9759 |
rs4852026 | snp | A/G | 0.499968 | 0.00399348 | intron-variant | HDAC4 | GRCh38.p7 | 2:239150606 | GCAGGAAGTCTCACC[A/G]CGCTGCACCTCCTGA | 9759 |
rs4852027 | snp | A/G | 0.5 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239150665 | GCAGGAAGTCTCACC[A/G]CACTGCACCTCCTGA | 9759 |
rs4852028 | snp | A/G | 0.5 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239150667 | AGGAAGTCTCACCAC[A/G]CTGCACCTCCTGAAG | 9759 |
rs4852029 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HDAC4 | GRCh38.p7 | 2:239165588 | GCCCTGGCCTGGTTC[A/G]GCCTCGCATGAGAGC | 9759 |
rs4852032 | snp | A/G | 0.421368 | 0.182025 | intron-variant | HDAC4 | GRCh38.p7 | 2:239188650 | CCTGAATGGAGACAT[A/G]CCCTACGTGCGACCC | 9759 |
rs4852034 | snp | A/G | 0.040671 | 0.13668 | intron-variant | HDAC4 | GRCh38.p7 | 2:239220947 | AAAAAGCCAGGGACC[A/G]ACCTTGGTACCGTGT | 9759 |
rs4852035 | snp | A/G | 0.457504 | 0.139435 | intron-variant | HDAC4 | GRCh38.p7 | 2:239253058 | ACAACACACATTCCC[A/G]TCACACTTCATACGC | 9759 |
rs4852036 | snp | C/T | 0.454664 | 0.143571 | intron-variant | HDAC4 | GRCh38.p7 | 2:239253123 | TAAGATATTAGAGTC[C/T]CGGGAACAAATCCAC | 9759 |
rs4852037 | snp | A/G | 0.318656 | 0.240388 | intron-variant | HDAC4 | GRCh38.p7 | 2:239255895 | GCTACACACTTGGGC[A/G]AAAGCAATTCTTTGT | 9759 |
rs4852038 | snp | A/G | 0.44638 | 0.154709 | intron-variant | HDAC4 | GRCh38.p7 | 2:239264071 | CAAAAGGGGGAAGAC[A/G]CAGCCCTGGAAAGGA | 9759 |
rs4852039 | snp | A/G | 0.35809 | 0.225425 | intron-variant | HDAC4 | GRCh38.p7 | 2:239264265 | CTCCACTGCGGAGGA[A/G]CAGATGCGCCTGCCA | 9759 |
rs4852040 | snp | C/T | 0.454784 | 0.1434 | intron-variant | HDAC4 | GRCh38.p7 | 2:239269230 | ATTCACACACCCACA[C/T]ACATTCACACATCTA | 9759 |
rs4852041 | snp | A/C | 0.499879 | 0.0077866 | intron-variant | HDAC4 | GRCh38.p7 | 2:239279662 | TCACACAGCCCCCAC[A/C]GTGCCTCCCACAAAT | 9759 |
rs4852042 | snp | A/G | 0.331642 | 0.236293 | intron-variant | HDAC4 | GRCh38.p7 | 2:239279750 | CCGCAGGGGGCATGG[A/G]ATGGGGGCGACTGAG | 9759 |
rs4852044 | snp | A/G | 0.446118 | 0.155041 | intron-variant | HDAC4 | GRCh38.p7 | 2:239294124 | TTGGGCAGAAAGCTC[A/G]TGGATGCTCCGTGCA | 9759 |
rs4852045 | snp | A/C | 0.446249 | 0.154875 | intron-variant | HDAC4 | GRCh38.p7 | 2:239294205 | GATCCACCTCTATCA[A/C]CTCCCAGTGACTCAG | 9759 |
rs4852046 | snp | C/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239321319 | aaatacaaaaaatta[C/G]ccgggcgtggtggcg | 9759 |
rs4852047 | snp | A/G | 0.364609 | 0.222182 | intron-variant | HDAC4 | GRCh38.p7 | 2:239326226 | catgccacaatacga[A/G]tgaaccctgacacat | 9759 |
rs4852048 | snp | A/G | 0.322245 | 0.239334 | intron-variant | HDAC4 | GRCh38.p7 | 2:239336906 | TCCACATCACACTTA[A/G]GTGTCGCATGTCCTG | 9759 |
rs4852050 | snp | C/T | 0.331179 | 0.236453 | intron-variant | HDAC4 | GRCh38.p7 | 2:239347766 | ATGATCTGCCCACCT[C/T]GGCCTCTCAAAGCAC | 9759 |
rs4852051 | snp | C/T | 0.422158 | 0.181278 | intron-variant | HDAC4 | GRCh38.p7 | 2:239348612 | TTCCGTCCACACTCC[C/T]GGTTTCATGCCAGGG | 9759 |
rs4852052 | snp | A/T | 0.499382 | 0.017561 | intron-variant | HDAC4 | GRCh38.p7 | 2:239350968 | TAAAATAATCAAGTG[A/T]ACTCAAACAATAATT | 9759 |
rs4852053 | snp | C/T | 0.471863 | 0.115225 | intron-variant | HDAC4 | GRCh38.p7 | 2:239355808 | GTTCTGTGTTCACTT[C/T]AATACTGGTCAATTA | 9759 |
rs4852054 | snp | A/G | 0.496681 | 0.0405994 | intron-variant | HDAC4 | GRCh38.p7 | 2:239358250 | GTGACTCAGTAATCT[A/G]CTTCCGTTCGTGTGG | 9759 |
rs4852055 | snp | A/G | 0.435694 | 0.167385 | intron-variant | HDAC4 | GRCh38.p7 | 2:239360183 | GCCCTTGACCAGGGA[A/G]GCCAGGACACCCTGA | 9759 |
rs4852056 | snp | A/G | 0.435119 | 0.16802 | intron-variant | HDAC4 | GRCh38.p7 | 2:239360327 | GCCGCAAGGGGACCC[A/G]GAGACCCCAGCCCCC | 9759 |
rs4852057 | snp | A/G | 0.406814 | 0.194704 | intron-variant | HDAC4 | GRCh38.p7 | 2:239366901 | ACCAGACTAAGTAAG[A/G]AAAGATCTCTTCCAC | 9759 |
rs4852060 | snp | C/G | 0.413914 | 0.188765 | intron-variant | HDAC4 | GRCh38.p7 | 2:239372007 | CAGAGCTGCAAAGCA[C/G]ACCAGGGCAGGGCGC | 9759 |
rs4852061 | snp | A/T | 0.421684 | 0.181726 | intron-variant | HDAC4 | GRCh38.p7 | 2:239376805 | AGGCATACGGCTGGG[A/T]GGCAGGGTCTCGGTG | 9759 |
rs4852062 | snp | C/G | 0.188946 | 0.24243 | intron-variant | HDAC4 | GRCh38.p7 | 2:239383168 | CACCCAAAGGCTCCC[C/G]TTGTCGAGGAAGATG | 9759 |
rs4852063 | snp | A/G | 0.220544 | 0.248259 | intron-variant | HDAC4 | GRCh38.p7 | 2:239391047 | CCATCAGACCGCTCG[A/G]GTCATCCTCAGGGCC | 9759 |
rs4991655 | snp | A/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239172299 | GTGAAAAAAAATATA[A/T]ATATATATATATATA | 9759 |
rs5026849 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239232767 | GGTGGCCCTTCCCTC[A/T]CCAAGCCAAGGGCGG | 9759 |
rs5026852 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239232807 | TCACCAAGCCAAGGG[C/T]GGCCCTTCCCTCACC | 9759 |
rs5839722 | in-del | -/C | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239104387 | GTGCCCACCATCACA[-/C]CTGGCTAATTTTTGT | 9759 |
rs5839723 | in-del | -/AC | 0.499891 | 0.00738737 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239156892 | GCCCCACCTCAACAG[-/AC]ACACCTTTTCCCTAG | 9759 |
rs5839724 | in-del | -/A | | | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239156896 | CACCTCAACAGACAC[-/A]CCTTTTCCCTAGGGT | 9759 |
rs5839727 | in-del | -/A | 0.234982 | 0.249549 | intron-variant | HDAC4 | GRCh38.p7 | 2:239174404 | GAATATTCATTCGGC[-/A]AAAAAAACTTATGAA | 9759 |
rs5839728 | in-del | -/C | 0.491104 | 0.0660973 | intron-variant | HDAC4 | GRCh38.p7 | 2:239183914 | CCAGAAAACTAGGTT[-/C]CTTTCCGTGTTAGTT | 9759 |
rs5839729 | in-del | -/CA/CACA | 0.203131 | 0.260681 | intron-variant | HDAC4 | GRCh38.p7 | 2:239206394 | ATGCACACATACGTG[-/CA/CACA]CACACACACACACAC | 9759 |
rs5839730 | in-del | -/G | | | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239232752 | CCTCACCAAGCCAAG[-/G]GTGGCCCTTCCCTCT | 9759 |
rs5839735 | in-del | -/C | 0.0759472 | 0.179459 | intron-variant | HDAC4 | GRCh38.p7 | 2:239235197 | GGAGCCCCCCGAACA[-/C]CCCCCCAAGAGGCCA | 9759 |
rs5839737 | in-del | -/G | 0.464416 | 0.128553 | intron-variant | HDAC4 | GRCh38.p7 | 2:239256885 | TACCATTCCATTTGT[-/G]TAGAATGCAGGTATA | 9759 |
rs5839738 | in-del | -/T | 0.0197687 | 0.0974348 | intron-variant | HDAC4 | GRCh38.p7 | 2:239274013 | CGGAAGACACCTGCA[-/T]TGACGGTAGAACTGC | 9759 |
rs5839739 | in-del | -/C | 0.0372196 | 0.131242 | intron-variant | HDAC4 | GRCh38.p7 | 2:239289727 | GGAGAGCAGAGAGCA[-/C]CCCCCAAAGTCCCCG | 9759 |
rs5839740 | in-del | -/CA | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239290705 | GCACACACACGCACG[-/CA]CACACTCACATACGC | 9759 |
rs5839741 | in-del | -/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239291035 | AAGAGCCGTTCAGAA[-/G]GCAGCGCCTGCCTCC | 9759 |
rs5839742 | in-del | -/A | 0.470521 | 0.117772 | intron-variant | HDAC4 | GRCh38.p7 | 2:239384452 | GACCCCTGTCTCTAC[-/A]AAAAAAAAAAAAAAA | 9759 |
rs6147245 | in-del | -/GAACGCAGCCCGCGT | 0.491316 | 0.0653198 | intron-variant | HDAC4 | GRCh38.p7 | 2:239391904 | AACAGAACTTCGTCA[-/GAACGCAGCCCGCGT]GTGCTGAAGCTGGCA | 9759 |
rs6543510 | snp | A/G | 0.277067 | 0.24853 | intron-variant | HDAC4 | GRCh38.p7 | 2:239102958 | TGCTTCAGCTCCACA[A/G]ACAGAAACTCCAACT | 9759 |
rs6543511 | snp | C/T | 0.473081 | 0.112848 | intron-variant | HDAC4 | GRCh38.p7 | 2:239125193 | GGACCTGGCAGGAGG[C/T]GGCTGGATCATGTGG | 9759 |
rs6543512 | snp | A/G | 0.481319 | 0.0948228 | intron-variant | HDAC4 | GRCh38.p7 | 2:239125372 | CCTTCGCCTACCACA[A/G]TTGAATGTTTCCTCG | 9759 |
rs6543513 | snp | A/C | 0.474544 | 0.10991 | intron-variant | HDAC4 | GRCh38.p7 | 2:239125520 | GCAGGAATGGCCTGA[A/C]ACAGGGACTCAGGTT | 9759 |
rs6543514 | snp | C/T | 0.314787 | 0.241459 | intron-variant | HDAC4 | GRCh38.p7 | 2:239174994 | gaaggggGAAGTGCA[C/T]AAGGACTTCTCTTCT | 9759 |
rs6543516 | snp | C/T | 0.268995 | 0.249277 | intron-variant | HDAC4 | GRCh38.p7 | 2:239209098 | gttgctcaggctggt[C/T]ttgaactcctgagct | 9759 |
rs6543517 | snp | A/G | 0.136506 | 0.222754 | intron-variant | HDAC4 | GRCh38.p7 | 2:239209548 | gattaagactcaaat[A/G]tgaaagacaaaatgt | 9759 |
rs6543518 | snp | A/G | 0.412249 | 0.190198 | intron-variant | HDAC4 | GRCh38.p7 | 2:239222589 | TTCTCATACAGAAGC[A/G]CAGCCATGAAAGACA | 9759 |
rs6543519 | snp | C/T | 0.479502 | 0.0991411 | intron-variant | HDAC4 | GRCh38.p7 | 2:239249261 | CAGGTCCGAAGGCCA[C/T]GGTAAGGACCTTCCA | 9759 |
rs6543520 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | HDAC4 | GRCh38.p7 | 2:239291652 | ACAACCTACAATTAA[C/G]ACAGGGACAATTATC | 9759 |
rs6543521 | snp | G/T | 0.195526 | 0.243993 | intron-variant, upstream-variant-2KB | HDAC4, MIR4269 | GRCh38.p7 | 2:239304947 | AGCAGAGAACACAGT[G/T]AGCATCACAGAGTCC | 9759 |
rs6543522 | snp | C/T | 0.443866 | 0.157848 | intron-variant | HDAC4 | GRCh38.p7 | 2:239306535 | GGGCCCCGACACACT[C/T]GTTTCGTACCTTTCC | 9759 |
rs6543523 | snp | A/G | 0.499477 | 0.0161657 | intron-variant | HDAC4 | GRCh38.p7 | 2:239306568 | GTCATGATACAAAAC[A/G]TAAGCTGGAAAGGGT | 9759 |
rs6543524 | snp | A/G | 0.490727 | 0.0674567 | intron-variant | HDAC4 | GRCh38.p7 | 2:239324815 | CGCAGCGACAGGGAC[A/G]GGAGCCAAAGAACAA | 9759 |
rs6543526 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | HDAC4 | GRCh38.p7 | 2:239330383 | TCCAAAGGCCTGAGC[A/G]AGGGCCACTGGGGCC | 9759 |
rs6543529 | snp | C/G | 0.387832 | 0.208572 | intron-variant | HDAC4 | GRCh38.p7 | 2:239380275 | GGGCATATGCACACA[C/G]ACGTCCGTGCACACA | 9759 |
rs6705378 | snp | A/G | 0.496175 | 0.0435625 | intron-variant | HDAC4 | GRCh38.p7 | 2:239272193 | TTAGCATTTACATTC[A/G]ACAGAAGCCAAAAGC | 9759 |
rs6706275 | snp | C/T | 0.254385 | 0.249962 | intron-variant | HDAC4 | GRCh38.p7 | 2:239343922 | AACGTGTCCAGCTCA[C/T]GTCACAGGCTATATG | 9759 |
rs6708882 | snp | A/G | 0.445592 | 0.155704 | intron-variant | HDAC4 | GRCh38.p7 | 2:239272704 | AACCTCTCGCAGCCA[A/G]CCATCTGCACTCACC | 9759 |
rs6710684 | snp | A/G | 0.394538 | 0.203982 | intron-variant | HDAC4 | GRCh38.p7 | 2:239106701 | CGGGGGGTAAGATGA[A/G]GCACAGATTAAAAGT | 9759 |
rs6711380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HDAC4 | GRCh38.p7 | 2:239167042 | GACCCAGATGGCCAG[C/T]TGTTGGAGGGGACTG | 9759 |
rs6712523 | snp | C/T | 0.445592 | 0.155704 | intron-variant | HDAC4 | GRCh38.p7 | 2:239272710 | TCGCAGCCAACCATC[C/T]GCACTCACCCCCAAT | 9759 |
rs6712730 | snp | C/G | 0.38821 | 0.208322 | intron-variant | HDAC4 | GRCh38.p7 | 2:239380493 | TGAGTTCACCACGGG[C/G]CTGACAGTAACCTTG | 9759 |
rs6712793 | snp | C/T | 0.11228 | 0.208646 | intron-variant | HDAC4 | GRCh38.p7 | 2:239368049 | caagatatctcatta[C/T]gtatacgcaaatact | 9759 |
rs6712996 | snp | C/T | 0.45889 | 0.13735 | intron-variant | HDAC4 | GRCh38.p7 | 2:239242994 | GGCCCAGGGGGTTTT[C/T]GGGAACAGGAAGGCA | 9759 |
rs6713685 | snp | C/G | 0.274929 | 0.248754 | intron-variant | HDAC4 | GRCh38.p7 | 2:239207922 | aaaaattacagtctt[C/G]gtcataaatacagtc | 9759 |
rs6714076 | snp | A/G | 0.132409 | 0.220618 | intron-variant | HDAC4 | GRCh38.p7 | 2:239148014 | ACAGAGGGGACAGGC[A/G]TGCACCTGGCACCAG | 9759 |
rs6714704 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | HDAC4 | GRCh38.p7 | 2:239072303 | gtttttttcaaaata[C/T]gcattttctacgaac | 9759 |
rs6715517 | snp | C/T | 0.367913 | 0.220446 | intron-variant | HDAC4 | GRCh38.p7 | 2:239100042 | taaaactggcatggc[C/T]gcaGGCCCCATGGAG | 9759 |
rs6716359 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HDAC4 | GRCh38.p7 | 2:239153512 | TGTTTGAAAGTAGAT[A/G]TCAAGGGTGATACAG | 9759 |
rs6717001 | snp | C/T | 0.212425 | 0.24716 | intron-variant | HDAC4 | GRCh38.p7 | 2:239145773 | GAACAGGCAGTGCAC[C/T]GCCTCCAGAGCAACA | 9759 |
rs6717473 | snp | C/G | 0.171704 | 0.237423 | intron-variant | HDAC4 | GRCh38.p7 | 2:239148441 | ACTTGTCCAGCTGAA[C/G]AGGAGCTGGACACGG | 9759 |
rs6719901 | snp | C/T | 0.443866 | 0.157848 | intron-variant | HDAC4 | GRCh38.p7 | 2:239246870 | TCCACTGCCCAGTGG[C/T]GAGGGCACATGTGGG | 9759 |
rs6719956 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239314916 | gatggggacgggcat[C/T]cagatgtgcctcatg | 9759 |
rs6719970 | snp | C/T | 0.138886 | 0.22395 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239314953 | tcctcccttttggaa[C/T]tgctgatagaacaga | 9759 |
rs6722812 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HDAC4 | GRCh38.p7 | 2:239222836 | TGAAGCAGGTCCCAG[C/T]GGGGACCTGGGTATC | 9759 |
rs6724175 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HDAC4, MIR4440 | GRCh38.p7 | 2:239069552 | CTTGCTTGGTGAGAG[G/T]GAGTCACAGTGCAAG | 9759 |
rs6724269 | snp | C/T | 0.368938 | 0.219895 | intron-variant | HDAC4 | GRCh38.p7 | 2:239099682 | CCCCAGCCCCAGCGG[C/T]GCTCCCCGCCTCCGC | 9759 |
rs6724280 | snp | G/T | | | intron-variant, upstream-variant-2KB | HDAC4, MIR4440 | GRCh38.p7 | 2:239069631 | GCCAGCAAGCCCCAC[G/T]GCACTTGCTTGGTGA | 9759 |
rs6724302 | snp | G/T | | | intron-variant, upstream-variant-2KB | HDAC4, MIR4440 | GRCh38.p7 | 2:239069680 | GCCAGCAAGCCCCAC[G/T]GCACTTGCTTGGTGA | 9759 |
rs6726499 | snp | A/G | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239261927 | AAAGCCTATGTCGGA[A/G]GGTCCTCGGGTTGCC | 9759 |
rs6728895 | snp | C/T | 0.173965 | 0.238157 | intron-variant | HDAC4 | GRCh38.p7 | 2:239148518 | CTGGGGACAAAGGCT[C/T]GGCCTTGAGAACAGT | 9759 |
rs6732098 | snp | C/T | 0.413083 | 0.189483 | intron-variant | HDAC4 | GRCh38.p7 | 2:239222880 | GCAGCCAGTAAGCAT[C/T]GTCACCTGGATTCAA | 9759 |
rs6732638 | snp | C/T | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239155241 | ACCCTAATAGGTGTA[C/T]TGGGAACATGGCCGG | 9759 |
rs6732673 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | HDAC4 | GRCh38.p7 | 2:239277508 | GTGCCAGTCACGCCA[C/T]GGTGGCCCATCGCTG | 9759 |
rs6733619 | snp | C/T | 0.469937 | 0.118861 | intron-variant | HDAC4 | GRCh38.p7 | 2:239248243 | TGAAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 9759 |
rs6734218 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | HDAC4 | GRCh38.p7 | 2:239285429 | AGCAAGGGGTTCCAC[C/T]GAGGCTGGGGCTTCG | 9759 |
rs6734425 | snp | C/G | 0.0637235 | 0.166737 | intron-variant | HDAC4 | GRCh38.p7 | 2:239285613 | TTCCTCTTCTGGGGA[C/G]GTGGCAGACAAGTCA | 9759 |
rs6735945 | snp | C/G | 0.040671 | 0.13668 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194122 | CATTCATCATTGAGC[C/G]TGGAGGAGATGCGCT | 9759 |
rs6737742 | snp | A/G | 0.274929 | 0.248754 | intron-variant | HDAC4 | GRCh38.p7 | 2:239294326 | CTGGGAGCTCCTGAT[A/G]GGCCTTGGCAGAGGC | 9759 |
rs6739116 | snp | A/G | 0.350764 | 0.228794 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194463 | TGAAGCTTGGGTGAC[A/G]CTCCTGCCCGCCTCA | 9759 |
rs6739632 | snp | A/G | 0.386504 | 0.209444 | intron-variant | HDAC4 | GRCh38.p7 | 2:239285324 | GCGGCTGGGCCCCCA[A/G]GTTCGCGGCTGTGCA | 9759 |
rs6740198 | snp | C/T | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239156965 | AAGCAAGCAAACATC[C/T]GATGCCCACATCCTC | 9759 |
rs6740794 | snp | A/G | 0.0321571 | 0.122656 | synonymous-codon | HDAC4 | GRCh38.p7 | 2:239189860 | GTGGAGCTGCGCCTC[A/G]TGCTGCCGGGAGAGC | 9759 |
rs6741059 | snp | C/G | 0.365024 | 0.221967 | intron-variant | HDAC4 | GRCh38.p7 | 2:239327360 | GGAGGCACCCCCATG[C/G]AGCTCAGAAACTGGG | 9759 |
rs6741795 | snp | C/T | 0.234982 | 0.249549 | intron-variant | HDAC4 | GRCh38.p7 | 2:239179476 | GGGATTTAGGATGCA[C/T]GGTCCTTATGAGAAT | 9759 |
rs6741865 | snp | G/T | 0.366885 | 0.220993 | intron-variant | HDAC4 | GRCh38.p7 | 2:239054321 | GGTCGGTGCCAGAAC[G/T]CAGAGGGCCTACACC | 9759 |
rs6742444 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | HDAC4 | GRCh38.p7 | 2:239200809 | CGTGCTCGGAGTGGC[A/G]TTCTCGGTGCAGAGT | 9759 |
rs6742576 | snp | A/G | 0.400325 | 0.199756 | intron-variant | HDAC4 | GRCh38.p7 | 2:239265936 | TGGGCCTGGTGGGAT[A/G]AGGTGAGGCCAAAGC | 9759 |
rs6742777 | snp | C/T | 0.20511 | 0.245937 | intron-variant | HDAC4 | GRCh38.p7 | 2:239132666 | CTCAGAGAGGTGAGA[C/T]CCATGCACACTCGAT | 9759 |
rs6742783 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | HDAC4 | GRCh38.p7 | 2:239201105 | ccccgcttgacaggt[A/G]tgggaaactgatgta | 9759 |
rs6743011 | snp | C/T | 0.162253 | 0.234095 | intron-variant | HDAC4 | GRCh38.p7 | 2:239132862 | GTTTTTAAAGACAGG[C/T]GAGAAACTCAGGTGT | 9759 |
rs6743546 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HDAC4 | GRCh38.p7 | 2:239292205 | TCAGTGTGGCTGGGG[A/G]CTCCCAGCCGGGCAG | 9759 |
rs6743553 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | HDAC4 | GRCh38.p7 | 2:239157386 | TGGCAGCTACTGATA[C/T]CCTGTGCCCAGGGAG | 9759 |
rs6743929 | snp | A/C | 0.277867 | 0.248442 | intron-variant | HDAC4 | GRCh38.p7 | 2:239092694 | GCTTCAGGACCACGG[A/C]TCCAGCTCCCAGGGA | 9759 |
rs6745266 | snp | A/G | 0.403509 | 0.197319 | intron-variant | HDAC4 | GRCh38.p7 | 2:239271879 | ACTTGTGTTTCGAGT[A/G]GGGGAAAAGCCACTA | 9759 |
rs6745354 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HDAC4 | GRCh38.p7 | 2:239293698 | TCTCTCCAGCTGATG[C/T]GCTTCTAGCTGCTGT | 9759 |
rs6748232 | snp | C/G | 0.114036 | 0.209795 | intron-variant | HDAC4 | GRCh38.p7 | 2:239189064 | GGTAATTTTGTTACA[C/G]AGATATAGATAACTT | 9759 |
rs6748376 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HDAC4 | GRCh38.p7 | 2:239162751 | AGCACAGCGGCTGCC[A/G]GAGTGGAGGACGTGG | 9759 |
rs6749348 | snp | A/G | 0.357024 | 0.225933 | intron-variant | HDAC4 | GRCh38.p7 | 2:239242720 | tgtttctgatcttac[A/G]aaggatatttcaatg | 9759 |
rs6749737 | snp | C/G | 0.153332 | 0.230554 | intron-variant | HDAC4 | GRCh38.p7 | 2:239368202 | agtgtgaagggctcc[C/G]gagtttgagaaccgT | 9759 |
rs6752136 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | HDAC4 | GRCh38.p7 | 2:239288612 | attggatataaaaat[A/G]aaatataaaaatcaa | 9759 |
rs6752438 | snp | A/C | 0.0224033 | 0.103439 | intron-variant | HDAC4 | GRCh38.p7 | 2:239190094 | TGTGGGAAAAACAAG[A/C]AGGAGAGCCGGTCAC | 9759 |
rs6752883 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HDAC4 | GRCh38.p7 | 2:239366170 | GTCGTCAGGGTCATG[C/T]GTGTGGCACTATGTG | 9759 |
rs6753167 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HDAC4 | GRCh38.p7 | 2:239062582 | CGGCTGAAAGCGAAG[G/T]TCCCTATTGTTATTT | 9759 |
rs6753325 | snp | A/G | 0.44252 | 0.159487 | intron-variant | HDAC4 | GRCh38.p7 | 2:239128302 | AATCCTAGCACTTTG[A/G]GAGGCCGAGGTGGGT | 9759 |
rs6754748 | snp | G/T | 0.00597455 | 0.054357 | intron-variant | HDAC4 | GRCh38.p7 | 2:239143712 | GAGTCCCTGTGTGAT[G/T]CCAATGCTCGCACAC | 9759 |
rs6754852 | snp | C/T | 0.368938 | 0.219895 | intron-variant | HDAC4 | GRCh38.p7 | 2:239100676 | agccgtgagtgccag[C/T]ataagggatctcagg | 9759 |
rs6755156 | snp | A/C | 0.277867 | 0.248442 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239311433 | GTCAGCTGTTCTGAT[A/C]CGCAGAACACATAAC | 9759 |
rs6755401 | snp | C/T | 0.138886 | 0.22395 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239311616 | AGAGGGACACTGTGA[C/T]CCATGACAGGAAAGG | 9759 |
rs6755496 | snp | C/T | 0.276267 | 0.248616 | intron-variant | HDAC4 | GRCh38.p7 | 2:239101152 | ACCTGCTTCCTACTG[C/T]TGTTCACTCCCTTCT | 9759 |
rs6756485 | snp | A/C | 0.17461 | 0.238362 | intron-variant | HDAC4 | GRCh38.p7 | 2:239366775 | CAGTGGGGTCCCAGG[A/C]AGATGGCTGCAACCC | 9759 |
rs6756979 | snp | C/T | 0.17332 | 0.23795 | intron-variant | HDAC4 | GRCh38.p7 | 2:239367117 | CCGTTTCTAAAAcag[C/T]ggtcctcataatgcg | 9759 |
rs6757396 | snp | A/C | 0.338976 | 0.23363 | intron-variant | HDAC4 | GRCh38.p7 | 2:239236324 | GCCAGGCAGTTGGTG[A/C]CTTTGGGAAGAACAC | 9759 |
rs6759400 | snp | C/T | 0.14933 | 0.228835 | intron-variant | HDAC4 | GRCh38.p7 | 2:239136889 | CGCCCCAGAGGAAAC[C/T]CTGCAACTCCCTTTA | 9759 |
rs6760848 | snp | C/T | 0.414245 | 0.188477 | intron-variant | HDAC4 | GRCh38.p7 | 2:239303073 | AGAGGTCATCACCTC[C/T]GCGTACTGAACAGAA | 9759 |
rs6761010 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HDAC4, MIR4440 | GRCh38.p7 | 2:239069593 | CCACTGCACTTGCTT[A/G]GTGAGAGTGAGTCAC | 9759 |
rs6761023 | snp | A/G | | | intron-variant, upstream-variant-2KB | HDAC4, MIR4440 | GRCh38.p7 | 2:239069632 | CCAGCAAGCCCCACT[A/G]CACTTGCTTGGTGAG | 9759 |
rs6761046 | snp | A/G | | | intron-variant, upstream-variant-2KB | HDAC4, MIR4440 | GRCh38.p7 | 2:239069681 | CCAGCAAGCCCCACT[A/G]CACTTGCTTGGTGAG | 9759 |
rs6761097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HDAC4 | GRCh38.p7 | 2:239368215 | ccggagtttgagaac[C/T]gTGGCTCTGCAGGTG | 9759 |
rs6761274 | snp | A/G | | | intron-variant, upstream-variant-2KB | HDAC4, MIR4440 | GRCh38.p7 | 2:239069789 | CCACTGCACTTGCTT[A/G]GTGAGAGGGAGTCAC | 9759 |
rs6761277 | snp | G/T | | | intron-variant, upstream-variant-2KB | HDAC4, MIR4440 | GRCh38.p7 | 2:239069797 | CTTGCTTGGTGAGAG[G/T]GAGTCACGGTGCAAG | 9759 |
rs6761279 | snp | A/G | 0.368938 | 0.219895 | intron-variant | HDAC4 | GRCh38.p7 | 2:239099884 | TTGCCCTGGGACagc[A/G]tgtcctccggtggct | 9759 |
rs6761340 | snp | G/T | 0.484421 | 0.0868729 | intron-variant | HDAC4 | GRCh38.p7 | 2:239240298 | ATAGACAAGCTGCGG[G/T]ACACAGCCAGCTGGA | 9759 |
rs7355652 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | HDAC4 | GRCh38.p7 | 2:239302772 | GCAGGAAGAACCATC[A/G]CTGCTCAAGGCAGTC | 9759 |
rs7355702 | snp | C/G | 0.170408 | 0.236992 | intron-variant, upstream-variant-2KB | HDAC4, MIR4269 | GRCh38.p7 | 2:239304079 | CAGGCCCAGCTCCCC[C/G]ACCCGTAAGCAGTTG | 9759 |
rs7556743 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | HDAC4 | GRCh38.p7 | 2:239202948 | TCCACGCCGCCTGAG[C/G]AGCAGCAGACTGATC | 9759 |
rs7557540 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | HDAC4 | GRCh38.p7 | 2:239072518 | GTCCCCACGGCCTCC[C/T]CAGCACACGCGTGTG | 9759 |
rs7559295 | snp | A/G | 0.417845 | 0.185278 | intron-variant | HDAC4 | GRCh38.p7 | 2:239306468 | TAATACCTGACCCAG[A/G]GCCAAGCTATCCTGT | 9759 |
rs7559584 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | HDAC4 | GRCh38.p7 | 2:239151420 | GCTTCCCCCCAAAAT[A/G]GAGGAAAACCCACCC | 9759 |
rs7561354 | snp | A/C | 0.227074 | 0.248947 | intron-variant | HDAC4 | GRCh38.p7 | 2:239202572 | ATGGGTGTGGCTGGT[A/C]TTCAACACAGGACTC | 9759 |
rs7564271 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HDAC4 | GRCh38.p7 | 2:239175041 | CTACAAGAGTAAATC[C/T]CTCTACTCTCCTTAC | 9759 |
rs7564713 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HDAC4 | GRCh38.p7 | 2:239199545 | atcctgagtgggtct[C/T]gtggcagcctccaaa | 9759 |
rs7564777 | snp | C/T | 0.167484 | 0.23599 | intron-variant | HDAC4 | GRCh38.p7 | 2:239202674 | GCGGTGGCAGGGCCA[C/T]GCAACATGGAGAATC | 9759 |
rs7566403 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HDAC4 | GRCh38.p7 | 2:239120376 | acagatacatatacc[C/T]gcagaggcacacaca | 9759 |
rs7566731 | snp | C/G | 0.432797 | 0.170544 | intron-variant | HDAC4 | GRCh38.p7 | 2:239245795 | ATTCAATATGTCTTT[C/G]CTGAGCATCTGCTGG | 9759 |
rs7567577 | snp | C/T | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239175634 | CAGATAGCAAGAGCA[C/T]GCTGCTGGCCCTCAC | 9759 |
rs7570607 | snp | A/G | 0.157642 | 0.232314 | intron-variant | HDAC4 | GRCh38.p7 | 2:239139953 | CCATGGTTTCAAAAA[A/G]GAAAGTATGATGCTG | 9759 |
rs7570805 | snp | C/T | 0.347694 | 0.230122 | intron-variant | HDAC4 | GRCh38.p7 | 2:239247160 | ATAACCGCGCTCCCT[C/T]GCTGCCGGGCCACCC | 9759 |
rs7570903 | snp | C/T | 0.369958 | 0.21934 | intron-variant | HDAC4 | GRCh38.p7 | 2:239247183 | GGCCACCCGCACAGC[C/T]GGGCAAACCAAAAGG | 9759 |
rs7571345 | snp | A/G | 0.349671 | 0.229272 | intron-variant | HDAC4 | GRCh38.p7 | 2:239330554 | AGGCTGCCAGTGACC[A/G]CGCACAGTGGTTGAA | 9759 |
rs7573580 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | HDAC4 | GRCh38.p7 | 2:239139610 | AGGGCAAGTGCAAAG[C/T]GGGGTCATTTCAAGC | 9759 |
rs7573680 | snp | C/T | 0.479014 | 0.100263 | intron-variant | HDAC4 | GRCh38.p7 | 2:239247381 | TTGGGGTGGAATATC[C/T]CCCCTGTCGAGTGGA | 9759 |
rs7574008 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | HDAC4 | GRCh38.p7 | 2:239307825 | CCCAGCCTGAAACGC[C/T]ACCCCACAGCCACTG | 9759 |
rs7574691 | snp | C/T | 0.195214 | 0.243923 | intron-variant | HDAC4 | GRCh38.p7 | 2:239122991 | TTAGGCGGCCCTGGG[C/T]AAGATTCTTGTCTTC | 9759 |
rs7575631 | snp | C/G/T | 0.0205511 | 0.0992634 | intron-variant | HDAC4 | GRCh38.p7 | 2:239383789 | GGCAGGAATGGACAA[C/G/T]AGAGACTGGAAAGTG | 9759 |
rs7579350 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | HDAC4 | GRCh38.p7 | 2:239062132 | TTTTCACTGCCCATA[C/G]TCACTGGCAGTTGCA | 9759 |
rs7580176 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | HDAC4 | GRCh38.p7 | 2:239387881 | CAATGGGCACTAAGG[A/G]GAGTGGAAGGCGTGG | 9759 |
rs7580301 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | HDAC4 | GRCh38.p7 | 2:239382737 | tctttttcttttttt[C/T]tttttagacgcagtt | 9759 |
rs7581200 | snp | A/G | 0.49975 | 0.0111793 | intron-variant | HDAC4 | GRCh38.p7 | 2:239162515 | GGACTGGCTCTGGGG[A/G]CACAGATCGGGGTCT | 9759 |
rs7581656 | snp | A/G | 0.332106 | 0.236133 | intron-variant | HDAC4 | GRCh38.p7 | 2:239107795 | AGGTGGGAGCGAAAC[A/G]TCAGGAAAGGTCACA | 9759 |
rs7584828 | snp | A/G | 0.450985 | 0.148678 | intron-variant | HDAC4 | GRCh38.p7 | 2:239258492 | GTAAACCAGAAAACA[A/G]TAATATCTTTCACAG | 9759 |
rs7585225 | snp | C/T | 0.27742 | 0.248492 | intron-variant | HDAC4 | GRCh38.p7 | 2:239108040 | GCCCACCTGCCCCGG[C/T]CGGCGTTACCTCGCA | 9759 |
rs7585378 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | HDAC4 | GRCh38.p7 | 2:239060487 | CAGGTGGCCAATAGG[C/T]AGATGCGGGGCTGCT | 9759 |
rs7587182 | snp | C/T | 0.081446 | 0.184634 | intron-variant | HDAC4 | GRCh38.p7 | 2:239387127 | gcacgtgcacacgca[C/T]gtacatgtgtgtTGA | 9759 |
rs7587542 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | HDAC4 | GRCh38.p7 | 2:239330922 | CCTTCTCCATCCCAA[A/G]AAGGCCACTGAAGAG | 9759 |
rs7587786 | snp | A/G | 0.400325 | 0.199756 | intron-variant | HDAC4 | GRCh38.p7 | 2:239264822 | GCCCACTGCTGCCCC[A/G]TCGGAGGGTCCTGCC | 9759 |
rs7588545 | snp | A/C | 0.308661 | 0.24302 | intron-variant | HDAC4 | GRCh38.p7 | 2:239386065 | AAGACCCGGCAGGCA[A/C]GGCAGAGGGGCCTGC | 9759 |
rs7588698 | snp | A/G | 0.206642 | 0.246211 | intron-variant | HDAC4 | GRCh38.p7 | 2:239120200 | TGGGAGACAGATCAG[A/G]ACTGGAGCAGTACGC | 9759 |
rs7588996 | snp | A/G | 0.387263 | 0.208947 | intron-variant | HDAC4 | GRCh38.p7 | 2:239164790 | GTTGTTAGAAACCAC[A/G]CTGCAGTGAACATTT | 9759 |
rs7589150 | snp | C/G | 0.111928 | 0.208413 | intron-variant | HDAC4 | GRCh38.p7 | 2:239392575 | TCACTAATTAAGATA[C/G]ACCCCGCTTGTGTGG | 9759 |
rs7589695 | snp | C/T | 0.408871 | 0.193029 | intron-variant | HDAC4 | GRCh38.p7 | 2:239332851 | GGAAAAATGAGAGAA[C/T]AAACAATATCAGGAA | 9759 |
rs7590833 | snp | A/G | 0.4983 | 0.0291038 | intron-variant | HDAC4 | GRCh38.p7 | 2:239361639 | AAGCAGCGCTATCTG[A/G]AGCCCACGAGGAAAG | 9759 |
rs7591120 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | HDAC4 | GRCh38.p7 | 2:239149514 | AACAAGCAAAGACGA[C/T]GCCCCACAGAAGAAC | 9759 |
rs7593103 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HDAC4, MGC16025 | GRCh38.p7 | 2:239196204 | GGAGACAGCACATCA[A/G]AAATGCATGACTTAG | 9759 |
rs7594398 | snp | C/T | 0.361894 | 0.223562 | intron-variant | HDAC4 | GRCh38.p7 | 2:239328761 | GACCTCTCGGGCGCC[C/T]GCTGGCCCTCTTTAT | 9759 |
rs7594553 | snp | A/G | 0.337841 | 0.23406 | intron-variant | HDAC4 | GRCh38.p7 | 2:239296289 | ATGTGTGCCCTGGGC[A/G]TGGACACCAGCACTC | 9759 |
rs7595357 | snp | A/C | 0.450609 | 0.149185 | intron-variant | HDAC4 | GRCh38.p7 | 2:239258640 | GAAGACATTCTCACA[A/C]CTGATCTCAGAGGGA | 9759 |
rs7599094 | snp | A/T | 0.477768 | 0.103061 | intron-variant | HDAC4 | GRCh38.p7 | 2:239357730 | ctcgacaaaaaataa[A/T]aaaaaaaaataagct | 9759 |
rs7599555 | snp | C/T | 0.338069 | 0.233974 | intron-variant | HDAC4 | GRCh38.p7 | 2:239164884 | CATCTAACAAACTTA[C/T]TATTCTAACCCTCGG | 9759 |
rs7602246 | snp | C/T | 0.145305 | 0.227022 | intron-variant | HDAC4 | GRCh38.p7 | 2:239235996 | AGTGAGCCAAGATTA[C/T]GCCACTCCACTCCAG | 9759 |
rs7604498 | snp | A/G | 0.256061 | 0.249927 | intron-variant | HDAC4 | GRCh38.p7 | 2:239164766 | CTTCCCGACTGGGAG[A/G]CAGTTTTGGTTGTTA | 9759 |
rs7605696 | snp | C/T | 0.100944 | 0.200705 | intron-variant | HDAC4 | GRCh38.p7 | 2:239141630 | CTGCCCCACCTGCAG[C/T]CCACCGTAGCCCACC | 9759 |
rs7607837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HDAC4 | GRCh38.p7 | 2:239289866 | TGCATAAACCCTCAC[C/T]TCATAATCATCCTTC | 9759 |
rs7608582 | snp | C/T | 0.215747 | 0.247642 | intron-variant | HDAC4 | GRCh38.p7 | 2:239398180 | CCTCTGCGGCTCCTT[C/T]GCGCCCTACATCAGG | 9759 |
rs9308908 | snp | C/T | 0.335559 | 0.234904 | intron-variant | HDAC4 | GRCh38.p7 | 2:239074483 | AGGCTTGGTGTGTGG[C/T]GTTGCCTCAAAGCCA | 9759 |
rs9308910 | snp | A/G | 0.330482 | 0.236691 | intron-variant | HDAC4 | GRCh38.p7 | 2:239290003 | AATAAAATTAACAAA[A/G]TTCTATCAACTACAG | 9759 |
rs9631045 | snp | A/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239158212 | TTTCTCTACCAAATA[A/G]TATTTTCAGATTGTA | 9759 |
rs9636379 | snp | A/G | 0.2768 | 0.248559 | intron-variant | HDAC4 | GRCh38.p7 | 2:239219744 | TGCAATCGAGATATC[A/G]GTATCACAAAGATTG | 9759 |
rs9677989 | snp | C/T | 0.252421 | 0.249988 | intron-variant | HDAC4 | GRCh38.p7 | 2:239120725 | GTGCCTGCCTTTCTT[C/T]AGCAGCCCAGGGGCC | 9759 |
rs9678428 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | HDAC4 | GRCh38.p7 | 2:239124028 | TGGAGTGAGGGGGGC[A/G]CTTTCACAGGAGAGA | 9759 |
rs9941534 | snp | C/T | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239215671 | TCTCTAATCTCCAGA[C/T]AGCAGACACCCCTTC | 9759 |
rs9941711 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | HDAC4 | GRCh38.p7 | 2:239215239 | TGAGGACTGGTGGCC[A/G]GGGCGGGGGAAGGTA | 9759 |
rs10164440 | snp | A/G | 0.174932 | 0.238463 | intron-variant | HDAC4 | GRCh38.p7 | 2:239366668 | CAGACAGACACACAG[A/G]AGGCCCAAGGATTTG | 9759 |
rs10166405 | snp | C/T | 0.205417 | 0.245993 | intron-variant | HDAC4 | GRCh38.p7 | 2:239135733 | AGCACCCAGCAGGCA[C/T]GGCAGAGCTATGCGG | 9759 |
rs10166651 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | HDAC4 | GRCh38.p7 | 2:239273729 | CACAGGCAGTGAGAG[C/T]TCTGCCGTGGCCACA | 9759 |
rs10167383 | snp | C/T | 0.175254 | 0.238565 | intron-variant | HDAC4 | GRCh38.p7 | 2:239366618 | AGACTTGTTTCCGTT[C/T]GCTGTGAAATAAAAG | 9759 |
rs10168053 | snp | A/G | 0.0283545 | 0.115643 | intron-variant | HDAC4 | GRCh38.p7 | 2:239066976 | TCGAGACACATGGCC[A/G]GGCCGGGTTTCGTTT | 9759 |
rs10168525 | snp | A/G | 0.106633 | 0.204807 | intron-variant | HDAC4 | GRCh38.p7 | 2:239273215 | caagggttatgtcca[A/G]aagactcaagggcca | 9759 |
rs10168537 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HDAC4 | GRCh38.p7 | 2:239116588 | ACCTCCAGCGTCAAC[A/G]CTTTGCAATCTTCTT | 9759 |
rs10168632 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HDAC4 | GRCh38.p7 | 2:239081810 | GCCTGGGCCCTGCCC[A/G]GAGGAAAACGGGCAC | 9759 |
rs10168694 | snp | A/C/G | 0.0382716 | 0.132943 | intron-variant, upstream-variant-2KB | HDAC4, MIR2467 | GRCh38.p7 | 2:239352670 | GAGAAGAAATGACCC[A/C/G]GCCTTACCTGGATGG | 9759 |
rs10168964 | snp | A/G | 0.0452352 | 0.143427 | synonymous-codon | HDAC4 | GRCh38.p7 | 2:239082177 | GTACAGGACGCTGGG[A/G]TCGCTGTAGAAAGCC | 9759 |
rs10169279 | snp | C/T | 0.490453 | 0.0684267 | intron-variant | HDAC4 | GRCh38.p7 | 2:239101379 | GAAGGCGTGAGCGAG[C/T]GAGTGAGTGAACGCA | 9759 |
rs10169764 | snp | C/T | 0.499104 | 0.0211472 | intron-variant | HDAC4 | GRCh38.p7 | 2:239339397 | AGGAGGCAATGGGCC[C/T]AGTCCAGGTCACCCC | 9759 |
rs10170311 | snp | C/G | 0.499121 | 0.020948 | intron-variant | HDAC4 | GRCh38.p7 | 2:239339934 | GGCCAGGGCCACCGG[C/G]CTTTGTGACTGCTTC | 9759 |
rs10170911 | snp | C/T | 0.426966 | 0.176587 | intron-variant | HDAC4 | GRCh38.p7 | 2:239242558 | GTAGTTATCGTGTat[C/T]ttctacatatagaat | 9759 |
rs10171344 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HDAC4 | GRCh38.p7 | 2:239239899 | CGGCCTTGGAGGCGG[C/T]GGCACAGACATGGGT | 9759 |
rs10171515 | snp | A/G | 0.175576 | 0.238665 | intron-variant | HDAC4 | GRCh38.p7 | 2:239368886 | TCGATGTCGGCATCG[A/G]CAGCTGAGGCTGCCC | 9759 |
rs10172353 | snp | C/T | 0.244776 | 0.249945 | intron-variant | HDAC4 | GRCh38.p7 | 2:239074834 | TCCACGACTTTCCTA[C/T]AAGAGGAAGCTGAAG | 9759 |
rs10173871 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | HDAC4 | GRCh38.p7 | 2:239104163 | AGCCAGGCAGGAGGG[A/T]CGTACTCTCTGGGTA | 9759 |
rs10174339 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | HDAC4 | GRCh38.p7 | 2:239273774 | AAGCTCCCCAACAAA[C/T]AGACTGGAGAGCAAG | 9759 |
rs10174432 | snp | G/T | 0.424348 | 0.179172 | intron-variant | HDAC4 | GRCh38.p7 | 2:239338810 | GCCACCAACCACATT[G/T]CAAAAGCCACTGGTG | 9759 |
rs10174562 | snp | C/T | 0.267364 | 0.249396 | utr-variant-3-prime | HDAC4 | GRCh38.p7 | 2:239050673 | CCCTGTAAACTTTAC[C/T]AAACTCCGAAACTCG | 9759 |
rs10175140 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | HDAC4 | GRCh38.p7 | 2:239384414 | agaccaggagctcaa[A/G]accagcctggacaac | 9759 |
rs10175200 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | HDAC4 | GRCh38.p7 | 2:239118532 | TGTCCACGGGTGAGC[A/G]TGCCGTTGGGAGAGG | 9759 |
rs10177607 | snp | C/T | 0.391397 | 0.206172 | intron-variant, upstream-variant-2KB | HDAC4, MIR4269 | GRCh38.p7 | 2:239304744 | CCAGGGGTAACTGCT[C/T]GCTTCTGAATCTCCT | 9759 |
rs10177619 | snp | A/T | 0.493881 | 0.054972 | intron-variant | HDAC4 | GRCh38.p7 | 2:239339635 | CTCCAGAGCAGAATC[A/T]TCCCAGAGAACCACA | 9759 |
rs10178347 | snp | C/G | 0.101301 | 0.200969 | intron-variant | HDAC4 | GRCh38.p7 | 2:239117069 | CTCATCGCACATTCA[C/G]TAAAAGGATGGGGCA | 9759 |
rs10178931 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | HDAC4 | GRCh38.p7 | 2:239290831 | TTCTATACAGGGCCT[A/G]GCCCACCTGAAAGTC | 9759 |
rs10179405 | snp | C/T | 0.332799 | 0.23589 | intron-variant | HDAC4 | GRCh38.p7 | 2:239347992 | TGCACTGCTTCCTAT[C/T]GAGAGCATCATCCCG | 9759 |
rs10180424 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | HDAC4 | GRCh38.p7 | 2:239122785 | TCACAGTGATGTTTC[C/T]AAAACAACTGCCCTC | 9759 |
rs10180874 | snp | A/G | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239361427 | ACTCCCAATGCCTCA[A/G]AGAGCCTGCAGAGGG | 9759 |
rs10181205 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | HDAC4 | GRCh38.p7 | 2:239215752 | GTGGACTGGCAAAGC[C/T]GTCTGCACCAGCGCC | 9759 |
rs10182074 | snp | C/T | 0.490063 | 0.0697833 | intron-variant | HDAC4 | GRCh38.p7 | 2:239324222 | AACCCAAATTGGACA[C/T]GCAAAGGCAAAAATG | 9759 |
rs10182187 | snp | C/T | 0.224116 | 0.248656 | intron-variant | HDAC4 | GRCh38.p7 | 2:239205973 | AAAGCAGCGGTCAGG[C/T]TGGGGCAGGATCCAT | 9759 |
rs10182344 | snp | A/G | 0.488545 | 0.074807 | intron-variant | HDAC4 | GRCh38.p7 | 2:239356959 | accctgctcttagta[A/G]ctgttagaacaagta | 9759 |
rs10182433 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HDAC4 | GRCh38.p7 | 2:239357058 | cactccataaacaac[A/G]gctgaatacacgtta | 9759 |
rs10183376 | snp | C/T | 0.315758 | 0.241197 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239308870 | CGAAAGACGGGTTCC[C/T]CTTCCTCTACACCCA | 9759 |
rs10183592 | snp | C/T | 0.363985 | 0.222503 | intron-variant, utr-variant-5-prime, splice-donor-variant, upstream-variant-2KB | HDAC4 | GRCh38.p7 | 2:239309074 | AGTTAATCGTACTGA[C/T]TTGGTGCTTTACCTT | 9759 |
rs10184565 | snp | A/G | 0.3512 | 0.228601 | intron-variant | HDAC4 | GRCh38.p7 | 2:239091996 | gaatggcgtgaaccc[A/G]ggaggcggagcttgc | 9759 |
rs10185139 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | HDAC4 | GRCh38.p7 | 2:239333260 | GATTTTACATTAAGT[A/G]GTTGGTaaaaaaaag | 9759 |
rs10185553 | snp | A/C | 0.312837 | 0.241974 | intron-variant | HDAC4 | GRCh38.p7 | 2:239082428 | GGTCGCAGGGGTTCT[A/C]AGGGCCAATGTTCGC | 9759 |
rs10186964 | snp | C/T | 0.448963 | 0.151372 | intron-variant | HDAC4 | GRCh38.p7 | 2:239347943 | TCATCCCGGTGACCA[C/T]AGACACGTCCCAGCA | 9759 |
rs10187175 | snp | C/G | 0.204803 | 0.245881 | intron-variant | HDAC4 | GRCh38.p7 | 2:239133122 | CAAAACAAAGATTGC[C/G]CCATTTGGCTTCTGG | 9759 |
rs10187459 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HDAC4 | GRCh38.p7 | 2:239318962 | GCCAAGGAACGGAAC[A/G]GCCCCAGTGGAACTG | 9759 |
rs10187532 | snp | C/T | 0.418974 | 0.184249 | intron-variant | HDAC4 | GRCh38.p7 | 2:239307682 | CCCTCCTCACTCAGA[C/T]GACGTTCTCATGACC | 9759 |
rs10187686 | snp | A/G | 0.154661 | 0.231107 | intron-variant | HDAC4 | GRCh38.p7 | 2:239187861 | GTGTTTGTTACACAC[A/G]GCTGCTAGGTCGCTC | 9759 |
rs10188303 | snp | A/C | 0.318415 | 0.240457 | intron-variant | HDAC4 | GRCh38.p7 | 2:239325702 | gggcgtggtggctca[A/C]gcctgtaatcccagc | 9759 |
rs10189342 | snp | A/G | 0.323434 | 0.238972 | intron-variant | HDAC4 | GRCh38.p7 | 2:239148723 | ACGTGCATGACCAAG[A/G]TGGCGAGGCCGCAGA | 9759 |
rs10189520 | snp | A/G | 0.319856 | 0.240042 | intron-variant | HDAC4 | GRCh38.p7 | 2:239329222 | TCAGAAGGGGTCCAC[A/G]GGGACCCCACCAGCT | 9759 |
rs10192336 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | HDAC4 | GRCh38.p7 | 2:239148859 | CAGAGGAGGGTCTCC[G/T]AGGTCTGCTGAAATG | 9759 |
rs10193548 | snp | C/T | 0.499087 | 0.0213463 | intron-variant | HDAC4 | GRCh38.p7 | 2:239079097 | GCCAGTTCTCTGGGG[C/T]GACAACTAAGTGAGG | 9759 |
rs10193575 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | HDAC4 | GRCh38.p7 | 2:239254802 | AGCATGCTAAGTCTC[A/T]ATTAGGATAAATAAG | 9759 |
rs10195361 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | HDAC4 | GRCh38.p7 | 2:239361903 | GATTAGAGAACTACG[A/G]TGATCACTTTTCTAA | 9759 |
rs10195501 | snp | C/G | 0.32768 | 0.237625 | intron-variant | HDAC4 | GRCh38.p7 | 2:239265631 | ACAGAGCAGGAACAC[C/G]AGGTGATGCCAATGC | 9759 |
rs10196133 | snp | G/T | 0.326506 | 0.238006 | intron-variant | HDAC4 | GRCh38.p7 | 2:239266183 | CCATAGCCCCTCGCC[G/T]GCATCCCAGCACAGT | 9759 |
rs10197122 | snp | C/T | 0.46875 | 0.121031 | intron-variant | HDAC4 | GRCh38.p7 | 2:239363622 | aatgttaaaggtaag[C/T]aatgaggcctggtct | 9759 |
rs10197739 | snp | G/T | 0.17332 | 0.23795 | intron-variant | HDAC4 | GRCh38.p7 | 2:239366566 | AATAAACTCTGGAGA[G/T]GAAGAGTCCAAATGG | 9759 |
rs10199413 | snp | C/G | 0.20511 | 0.245937 | intron-variant | HDAC4 | GRCh38.p7 | 2:239133749 | TGGGATTACAGGTGT[C/G]AGTCACCGTGTCCGG | 9759 |
rs10200378 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | HDAC4 | GRCh38.p7 | 2:239372946 | TCAATACCATGTCTC[A/G]GGGGAGTCCGTCACG | 9759 |
rs10200850 | snp | A/G | 0.324382 | 0.238678 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239313206 | ACAGATGTTCTCAGC[A/G]GCAGAGCCTGGCTTC | 9759 |
rs10201155 | snp | A/G | 0.213635 | 0.247341 | intron-variant | HDAC4 | GRCh38.p7 | 2:239133211 | AAACAAGAAAACACC[A/G]AAATCCACCAGACTA | 9759 |
rs10201188 | snp | A/G | 0.213937 | 0.247385 | intron-variant | HDAC4 | GRCh38.p7 | 2:239133275 | CCCCTAGCCCCACGC[A/G]TCCTGCAGCGCAGCC | 9759 |
rs10201317 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | HDAC4 | GRCh38.p7 | 2:239272818 | GACAAGAGCAGCAGA[A/G]GGGCTCACCTCTGTA | 9759 |
rs10201558 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | HDAC4 | GRCh38.p7 | 2:239273042 | TACATCCTCATTCCC[A/G]GAACCTAGAAATACA | 9759 |
rs10203767 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | HDAC4 | GRCh38.p7 | 2:239343836 | ATTGGCCTCTGATGC[A/G]CTGCCCAGCCTCAGC | 9759 |
rs10204440 | snp | A/G | 0.213937 | 0.247385 | intron-variant | HDAC4 | GRCh38.p7 | 2:239134177 | TCCAAAGGCAGGCGA[A/G]GGCGGGGCACCATCC | 9759 |
rs10204505 | snp | A/G | 0.359787 | 0.224604 | intron-variant, upstream-variant-2KB | HDAC4, MIR4269 | GRCh38.p7 | 2:239303760 | CCTCACTCTTCAAAA[A/G]CGACTGCGACAGCTG | 9759 |
rs10205271 | snp | A/G | 0.285257 | 0.247501 | intron-variant | HDAC4 | GRCh38.p7 | 2:239214226 | CCTTCTCTAGCTTCC[A/G]GAGGCTGCCATGTCC | 9759 |
rs10206855 | snp | C/G | 0.16911 | 0.236552 | intron-variant | HDAC4 | GRCh38.p7 | 2:239366441 | ATGTCAGCACTGAGG[C/G]CCTTTTGCAGATGCC | 9759 |
rs10207397 | snp | A/G | 0.0314385 | 0.121371 | intron-variant, downstream-variant-500B | HDAC4, MIR4440 | GRCh38.p7 | 2:239068400 | GCCCTTCCTTATCTC[A/G]TTATTAAAAAGGGGA | 9759 |
rs10207474 | snp | C/T | 0.0739136 | 0.177464 | intron-variant | HDAC4 | GRCh38.p7 | 2:239134235 | TGCACCCAGGCCCAT[C/T]TGTGCTCACCTGTGA | 9759 |
rs10208460 | snp | A/C | 0.0655868 | 0.168795 | intron-variant | HDAC4 | GRCh38.p7 | 2:239297081 | TGCTTCCTACAAGGG[A/C]TGGCCTATGCATCCT | 9759 |
rs10208676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HDAC4 | GRCh38.p7 | 2:239144305 | CTGACTGCATCTCCC[A/G]CAGTGCCAAGCTGGG | 9759 |
rs10208713 | snp | C/T | 0.297382 | 0.245469 | intron-variant | HDAC4 | GRCh38.p7 | 2:239267222 | GGGCAGTGCCCGGCC[C/T]ACAGAAAGTTCCCAT | 9759 |
rs10208802 | snp | C/T | 0.399073 | 0.200692 | intron-variant | HDAC4 | GRCh38.p7 | 2:239088780 | GCTTTCCAGTGAAAA[C/T]TACAAGTTTGGAACA | 9759 |
rs10208855 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | HDAC4 | GRCh38.p7 | 2:239166365 | CTCAGGGCTCTCTGT[C/T]GGTCTGAGAAAATCA | 9759 |
rs10209084 | snp | G/T | 0.460702 | 0.134554 | intron-variant | HDAC4 | GRCh38.p7 | 2:239089068 | gaggccacgatttga[G/T]ttcagatccacactg | 9759 |
rs10209224 | snp | G/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239174989 | ttggggaaggggGAA[G/T]TGCATAAGGACTTCT | 9759 |
rs10209266 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | HDAC4 | GRCh38.p7 | 2:239380854 | CCACTCGGCCTTCAC[A/G]TCCCATCTCAGAAAA | 9759 |
rs10209343 | snp | C/T | 0.371987 | 0.218218 | intron-variant | HDAC4 | GRCh38.p7 | 2:239342525 | TGAAAAAAACAAATA[C/T]GTTACAATAAGTTTT | 9759 |
rs10209850 | snp | C/T | 0.416218 | 0.186739 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239312972 | CTCTCAGGCCCCACG[C/T]TCCTCTCACTGGCTG | 9759 |
rs10209938 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HDAC4 | GRCh38.p7 | 2:239343130 | TTAAAAGCTCAGGGC[C/T]AGATATAATTCAAAA | 9759 |
rs10210263 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HDAC4 | GRCh38.p7 | 2:239134756 | TCTGATATATGAGCG[C/T]AAACGTACATGTAAC | 9759 |
rs10210496 | snp | C/T | 0.0382325 | 0.13287 | intron-variant | HDAC4 | GRCh38.p7 | 2:239066914 | CGCAGCCAGCACAGC[C/T]CAGAAACGCGTCTCA | 9759 |
rs10210839 | snp | C/T | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239368175 | tctttggagtccatg[C/T]taatttgcaggagtg | 9759 |
rs10211084 | snp | A/G | 0.31014 | 0.242659 | intron-variant | HDAC4 | GRCh38.p7 | 2:239341889 | AAGTGGGGCCTCTGG[A/G]GAGTGATTAAGTTAT | 9759 |
rs10211157 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HDAC4 | GRCh38.p7 | 2:239243253 | cgcctcccaggttca[C/T]gccattctcctgcct | 9759 |
rs10211599 | snp | C/T | 0.297382 | 0.245469 | intron-variant | HDAC4 | GRCh38.p7 | 2:239142610 | TCAGCACTGATCACG[C/T]CCTGCCACGCATGGC | 9759 |
rs10460499 | snp | C/T | 0.358303 | 0.225323 | intron-variant | HDAC4 | GRCh38.p7 | 2:239291308 | AGGGCCAAGTGCACA[C/T]GGGGATGGGCCTTGC | 9759 |
rs10460500 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | HDAC4 | GRCh38.p7 | 2:239291432 | CCCTGGGTGGCGGGG[G/T]GCCTGAGGGCACACA | 9759 |
rs10530231 | in-del | -/A | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239321491 | AAAAAAAAAAAAAAA[-/A]GGTTAGCTTACATTT | 9759 |
rs10535738 | in-del | -/TA | 0.499933 | 0.00579035 | intron-variant | HDAC4 | GRCh38.p7 | 2:239216191 | AAAAACGCACGTGTT[-/TA]TATATATACACACAC | 9759 |
rs10543545 | in-del | -/A | 0.27008 | 0.249192 | intron-variant | HDAC4 | GRCh38.p7 | 2:239109610 | GATGGGACTTCTGGT[-/A]AAAAAAAAAAAAAAG | 9759 |
rs10551133 | in-del | -/CTCT | 0.0607341 | 0.163335 | intron-variant | HDAC4 | GRCh38.p7 | 2:239384293 | TATTTTAGTACCTCT[-/CTCT]ATCATATGGAAATGT | 9759 |
rs10552393 | in-del | -/ACAC | 0.432357 | 0.171014 | intron-variant | HDAC4 | GRCh38.p7 | 2:239079842 | CACACACAGCGATAT[-/ACAC]ACAAAGACATGTGCA | 9759 |
rs10572423 | in-del | -/TTT | 0.399611 | 0.200291 | intron-variant | HDAC4 | GRCh38.p7 | 2:239070928 | atgcagtctctgttg[-/TTT]ttttttttttttttt | 9759 |
rs10596307 | in-del | -/AGTG | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239387081 | TGTCCGGGGAGCACG[-/AGTG]TGTGGGTGGGAATGC | 9759 |
rs10602135 | in-del | -/AT | 0.388398 | 0.208197 | intron-variant | HDAC4 | GRCh38.p7 | 2:239380344 | TACATTAAATTATAC[-/AT]ATGTTATAAATACAC | 9759 |
rs10622509 | in-del | -/TCCC | 0.457504 | 0.139435 | intron-variant | HDAC4 | GRCh38.p7 | 2:239294289 | CACTCAGGGAAGCTG[-/TCCC]GTTCGCCGTGAGGAC | 9759 |
rs10623712 | in-del | -/AAAC | 0.5 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239320421 | ATAAATCAAACAAAC[-/AAAC]AAAAAAATTTAGAAG | 9759 |
rs10629563 | in-del | -/AC | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239398084 | CCCCATCCCCAGCTA[-/AC]GTCATCAATTCTGAG | 9759 |
rs10674168 | in-del | -/CAGACA | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239278173 | CAAATTATCCCACCA[-/CAGACA]TTAGAGAAAAAAAGA | 9759 |
rs10690859 | in-del | -/CCCT/TCCC | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239294290 | ACTCAGGGAAGCTGT[-/CCCT/TCCC]TCGCCGTGAGGACGT | 9759 |
rs10715561 | in-del | -/G | 0.351853 | 0.228311 | intron-variant | HDAC4 | GRCh38.p7 | 2:239095280 | TGGGTCACAGACCCT[-/G]GTGGGGACACCTCAA | 9759 |
rs10716644 | in-del | -/A | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239222554 | AAAAAAAAAAAAAAA[-/A]TGGTGAAATGTGCTT | 9759 |
rs10719385 | in-del | -/A | 0.461148 | 0.133852 | intron-variant | HDAC4 | GRCh38.p7 | 2:239269991 | ATCTCCCCGCCCCCC[-/A]AAATGATGTCCTTAC | 9759 |
rs10865080 | snp | A/G | 0.423726 | 0.179776 | intron-variant | HDAC4 | GRCh38.p7 | 2:239334349 | ACATGGTGACGCCCC[A/G]TCTCTACAAAAAATA | 9759 |
rs10865082 | snp | A/C | 0.498734 | 0.0251279 | intron-variant | HDAC4 | GRCh38.p7 | 2:239365795 | TGCACAGACCAGGGT[A/C]GTCAGGGTCACACGT | 9759 |
rs11124180 | snp | C/G | 0.270621 | 0.249148 | intron-variant | HDAC4 | GRCh38.p7 | 2:239110213 | ACCACTGGGGAGTGG[C/G]ATTACGGGCAAACGG | 9759 |
rs11124182 | snp | A/C | 0.172674 | 0.237741 | intron-variant | HDAC4 | GRCh38.p7 | 2:239163707 | CTCCTTCCCTGCCTC[A/C]GGTGAAGAGCTGGCT | 9759 |
rs11124183 | snp | A/C | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239165217 | aatgcgagtttagac[A/C]ctgtctcaaaagaaa | 9759 |
rs11124184 | snp | C/G | 0.499451 | 0.0165644 | intron-variant | HDAC4 | GRCh38.p7 | 2:239165265 | TCTCTACACGCTGAC[C/G]CCCTGAACCACCCAT | 9759 |
rs11124187 | snp | A/C/G | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239201070 | CTTTAGTGCTGATGT[A/C/G]TTAATTCATTTAAGG | 9759 |
rs11124188 | snp | C/T | 0.406814 | 0.194704 | intron-variant | HDAC4 | GRCh38.p7 | 2:239216262 | TATGTAGTATTTATG[C/T]GGAAGATTCCATTCA | 9759 |
rs11124189 | snp | A/G | 0.475348 | 0.108251 | intron-variant | HDAC4 | GRCh38.p7 | 2:239295164 | TACAAAAAATTAGCC[A/G]GGCGTAGTGGCGGGC | 9759 |
rs11124190 | snp | C/G | 0.308661 | 0.24302 | intron-variant | HDAC4 | GRCh38.p7 | 2:239301385 | GAGAGCAGCAGCCCA[C/G]AGCCAGTGATGCCAG | 9759 |
rs11124191 | snp | A/G | 0.390464 | 0.206809 | intron-variant | HDAC4 | GRCh38.p7 | 2:239301386 | AGAGCAGCAGCCCAC[A/G]GCCAGTGATGCCAGG | 9759 |
rs11124192 | snp | C/T | 0.314787 | 0.241459 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239312970 | TGCTCTCAGGCCCCA[C/T]GCTCCTCTCACTGGC | 9759 |
rs11124194 | snp | C/T | 0.466204 | 0.125522 | intron-variant | HDAC4 | GRCh38.p7 | 2:239368799 | TTGCGTTCTTTCGGA[C/T]CAAAGCAGTAAATAA | 9759 |
rs11124195 | snp | C/G | 0.333952 | 0.235483 | intron-variant | HDAC4 | GRCh38.p7 | 2:239377481 | GCCTCTCTGGACCCT[C/G]CTGGAGGCCCTGTCT | 9759 |
rs11124196 | snp | C/T | 0.47709 | 0.104548 | intron-variant | HDAC4 | GRCh38.p7 | 2:239387730 | CCAGAGCAGCTGGAA[C/T]GTGGCTCCACCAAGA | 9759 |
rs11277127 | in-del | -/A | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239286546 | GAAGGAAGGGAAGGA[-/A]GGAAGACTATGGAGC | 9759 |
rs11281622 | in-del | -/CTGGACC | 0.493247 | 0.0577133 | intron-variant | HDAC4 | GRCh38.p7 | 2:239289590 | CAGAGGTCTTTTCTT[-/CTGGACC]TCTGGAAATCCAGGC | 9759 |
rs11343522 | in-del | -/A | 0.5 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239320403 | AAAAAAAAAAAAAAA[-/A]GTGATAAATCAAACA | 9759 |
rs11366042 | in-del | -/A | 0.5 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239092257 | CTGTCTCCAAAGAGG[-/A]AAAAAAAAAAAAAAA | 9759 |
rs11374131 | in-del | -/C | 0.166832 | 0.235761 | intron-variant | HDAC4 | GRCh38.p7 | 2:239163089 | TGCTCTGTGAACTCT[-/C]CCCCCGAAGGCCTTC | 9759 |
rs11396312 | in-del | -/A | 0.416382 | 0.186593 | intron-variant | HDAC4 | GRCh38.p7 | 2:239249778 | AAGAAAAAAAAAAAA[-/A]CAAGGAGCTGAATAT | 9759 |
rs11402529 | in-del | -/A | 0.35207 | 0.228214 | intron-variant | HDAC4 | GRCh38.p7 | 2:239286738 | CAGTGAGACACAGAC[-/A]AGACAAGGAAGGAGC | 9759 |
rs11432561 | in-del | -/C | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239213245 | GAGGGGCGGGCGGGG[-/C]CACAGCCACAAGGAC | 9759 |
rs11455611 | in-del | -/A/AA | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239222535 | AAAAAAAAAAAAAAA[-/A/AA]TGGTGAAATGTGCTT | 9759 |
rs11456343 | in-del | -/C | 0.132751 | 0.2208 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239225743 | GCCCGTGGCCACGTA[-/C]CTGCTACCCAAGGGA | 9759 |
rs11673904 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | HDAC4 | GRCh38.p7 | 2:239143069 | TCCTGGATGGTCTCA[C/T]GTGTGATGTGCTGCT | 9759 |
rs11674551 | snp | C/T | 0.145642 | 0.227177 | intron-variant | HDAC4 | GRCh38.p7 | 2:239135496 | CAAATTGGCAAACAC[C/T]TTTGAAACATGGTAA | 9759 |
rs11675157 | snp | A/C | 0 | 0 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239298660 | GCCGTGAGACTGTGG[A/C]TAAATCATTTATCCA | 9759 |
rs11675165 | snp | C/T | 0.2776 | 0.248472 | intron-variant | HDAC4 | GRCh38.p7 | 2:239095953 | TCCAGGGAGACTGGC[C/T]TGATGTAACAGGCTC | 9759 |
rs11675596 | snp | C/T | 0.116488 | 0.211364 | intron-variant | HDAC4 | GRCh38.p7 | 2:239198506 | CAGTGACTAGCCCCC[C/T]GTTCTTGCTGCAGTA | 9759 |
rs11675637 | snp | A/G | 0.319856 | 0.240042 | intron-variant | HDAC4 | GRCh38.p7 | 2:239322437 | TAGTAGGACCCATCC[A/G]TAGGCTGTTGTGGGG | 9759 |
rs11675700 | snp | A/C | 0.146314 | 0.227484 | intron-variant | HDAC4 | GRCh38.p7 | 2:239138612 | AGCGTACCCCTCCCA[A/C]CCCTGCCCTGCAGTC | 9759 |
rs11677357 | snp | A/G | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239173577 | gcccctacagaaaac[A/G]tggcacctaacagta | 9759 |
rs11677464 | snp | A/G | 0.136847 | 0.222927 | intron-variant | HDAC4 | GRCh38.p7 | 2:239143660 | CAGGGCCCTGTATTT[A/G]GCGGGTAGGTCTGGC | 9759 |
rs11678103 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HDAC4 | GRCh38.p7 | 2:239104100 | GGTCCCATCCACATA[A/G]CCTAGTGCTGCTTCT | 9759 |
rs11679247 | snp | G/T | 0.155656 | 0.231515 | intron-variant | HDAC4 | GRCh38.p7 | 2:239168616 | GTGTTTTCAAATGCT[G/T]AGATGCTGGCGGTGC | 9759 |
rs11680120 | snp | A/G | 0.5 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239150568 | CACCTCCTCAAGTAT[A/G]TACCACACCTTCACA | 9759 |
rs11680390 | snp | G/T | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239350311 | TAAAGCAAAAAATGG[G/T]TATTAATGTAAAAAG | 9759 |
rs11680524 | snp | C/T | 0.355954 | 0.226437 | intron-variant | HDAC4 | GRCh38.p7 | 2:239320542 | AGGACTCTTCTGTTA[C/T]GTAAAAATATGTATT | 9759 |
rs11680537 | snp | A/G | 0.155987 | 0.23165 | intron-variant | HDAC4 | GRCh38.p7 | 2:239150089 | CGTTGAGCTTCATAC[A/G]TAAAAATGGAATAAT | 9759 |
rs11680658 | snp | A/C | 0.497329 | 0.0364438 | intron-variant | HDAC4 | GRCh38.p7 | 2:239377925 | CTGCTTGGTTTTACA[A/C]CCACCTCAAGGACCT | 9759 |
rs11680981 | snp | C/T | 0.157972 | 0.232445 | intron-variant | HDAC4 | GRCh38.p7 | 2:239247551 | CCAGGGCATCTGAGC[C/T]GAACAAGCTGCTCAC | 9759 |
rs11680988 | snp | C/T | 0.27893 | 0.24832 | intron-variant | HDAC4 | GRCh38.p7 | 2:239277673 | CACACAGCCGCCCAG[C/T]CTGGTGTAGCCACAA | 9759 |
rs11681247 | snp | A/G | 0.422 | 0.181428 | intron-variant | HDAC4 | GRCh38.p7 | 2:239185409 | GCCTCCTGGGGAGAG[A/G]TGTACCCTAACTGCT | 9759 |
rs11681283 | snp | G/T | 0.146314 | 0.227484 | intron-variant | HDAC4 | GRCh38.p7 | 2:239185527 | GTGCACAGTGTGGGG[G/T]GTGCCCTGTGCCTCC | 9759 |
rs11681339 | snp | G/T | 0.170084 | 0.236883 | intron-variant | HDAC4 | GRCh38.p7 | 2:239180389 | CCCACTGCTGAGGAC[G/T]CAGCCGGTTTCCACG | 9759 |
rs11681412 | snp | C/T | 0.49995 | 0.00499176 | intron-variant | HDAC4 | GRCh38.p7 | 2:239275654 | CACACCTGGGTTCGG[C/T]ACTGCCACCCTGCGA | 9759 |
rs11682101 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HDAC4 | GRCh38.p7 | 2:239080934 | GCCAAGATTCCACGC[C/T]TGGCACTGAAGAATG | 9759 |
rs11682879 | snp | C/T | 0.122758 | 0.215196 | intron-variant | HDAC4 | GRCh38.p7 | 2:239124065 | ACGGAGAAATGATTC[C/T]GTCTGTCGCCAAATC | 9759 |
rs11683046 | snp | A/C | 0.269267 | 0.249256 | intron-variant | HDAC4 | GRCh38.p7 | 2:239277319 | GGCCTTTCCAAAGGC[A/C]CAAGGGTGAGAGGTG | 9759 |
rs11683224 | snp | A/G | 0.34659 | 0.230587 | intron-variant | HDAC4 | GRCh38.p7 | 2:239332875 | tcaggaatttaaaag[A/G]ggatgacactacaaa | 9759 |
rs11685604 | snp | A/G | 0.325799 | 0.238232 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239193681 | AGCAGCCAAGAGCGC[A/G]AGGGGAAGCAGCAGC | 9759 |
rs11685857 | snp | A/G | 0.144296 | 0.226554 | intron-variant | HDAC4 | GRCh38.p7 | 2:239133982 | ACAGAAACCCAAATC[A/G]CAAGAGCCGGTGGCC | 9759 |
rs11685880 | snp | C/T | 0.167484 | 0.23599 | intron-variant | HDAC4 | GRCh38.p7 | 2:239223942 | GAGAGTTCATGTCCA[C/T]GTATCTTTCTGCTAT | 9759 |
rs11686104 | snp | A/G | 0.2776 | 0.248472 | intron-variant | HDAC4 | GRCh38.p7 | 2:239364451 | CTACTGTAGGGCTCC[A/G]TGTGCATAAAATGTG | 9759 |
rs11686355 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | HDAC4 | GRCh38.p7 | 2:239386776 | AAGGCTGGCCCTTGT[C/T]CAGAGACAGCCCAGT | 9759 |
rs11687909 | snp | A/G | 0.437683 | 0.165152 | intron-variant | HDAC4 | GRCh38.p7 | 2:239185634 | CACTCACCAGCCTGG[A/G]GCATGCTCTAGCCAT | 9759 |
rs11687913 | snp | C/T | 0.445855 | 0.155373 | intron-variant | HDAC4 | GRCh38.p7 | 2:239124867 | GACATTCTGGTGTGC[C/T]GGCGTGTGGCCGCGT | 9759 |
rs11688627 | snp | G/T | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239141105 | TGGAGGCATGGAGCA[G/T]CAACATCACTCGTCC | 9759 |
rs11688812 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | HDAC4, MIR4440 | GRCh38.p7 | 2:239070537 | TTCATGTCTCCTTTA[A/G]GCTGCCGCCTTCGAT | 9759 |
rs11689462 | snp | G/T | 0.369346 | 0.219673 | intron-variant | HDAC4 | GRCh38.p7 | 2:239096029 | ACCCCCCGCTGTGGG[G/T]CTCCTCTCCCATTCT | 9759 |
rs11689823 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | HDAC4 | GRCh38.p7 | 2:239201394 | CAGAACTTCTGCTCC[A/G]GAGTCGATGGTCTTC | 9759 |
rs11689916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HDAC4 | GRCh38.p7 | 2:239234279 | CAAACACTCCCACCA[C/T]GCCCACCAACCCATG | 9759 |
rs11690216 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HDAC4, MGC16025 | GRCh38.p7 | 2:239196346 | CAATGAGGCCCAAAC[A/G]TCACCCTCTGCGTCC | 9759 |
rs11690847 | snp | C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239088374 | CGGACGCCGCAGGGA[C/T]CAGGCTCAGGAAGGG | 9759 |
rs11691535 | snp | A/G | 0.451483 | 0.148002 | intron-variant | HDAC4 | GRCh38.p7 | 2:239267736 | GACGAGGCCCCTCAC[A/G]AAGAGCTCTGCCCTG | 9759 |
rs11691856 | snp | C/T | 0.20111 | 0.245173 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239230063 | gagtcagggtggaac[C/T]gggaatcttactgct | 9759 |
rs11692243 | snp | A/G | 0.393987 | 0.204372 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239193676 | GGGAGAGCAGCCAAG[A/G]GCGCGAGGGGAAGCA | 9759 |
rs11692633 | snp | G/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239092862 | ttctttttttttttg[G/T]tttcttttcctttct | 9759 |
rs11693183 | snp | C/T | 0.368529 | 0.220116 | intron-variant | HDAC4 | GRCh38.p7 | 2:239100455 | aacttgtccacgtta[C/T]gtggatgtggcatcc | 9759 |
rs11693243 | snp | C/T | 0.368529 | 0.220116 | intron-variant | HDAC4 | GRCh38.p7 | 2:239100529 | tctgcccccagcctc[C/T]ttcccctgtgtggct | 9759 |
rs11693500 | snp | A/G | 0.34989 | 0.229177 | intron-variant | HDAC4 | GRCh38.p7 | 2:239198405 | CTGTCCACGAGAGGC[A/G]CCTCTCCATCCTGGG | 9759 |
rs11693556 | snp | C/T | 0.349452 | 0.229367 | intron-variant, upstream-variant-2KB | HDAC4, MGC16025 | GRCh38.p7 | 2:239196235 | CTACAATGTCCTTCA[C/T]CCTTTATTTATTGTG | 9759 |
rs11693641 | snp | A/C | 0.496905 | 0.0392151 | intron-variant | HDAC4 | GRCh38.p7 | 2:239330042 | TGGCCCCTGCCCTCC[A/C]AGCCCAAGCTGCTGC | 9759 |
rs11693783 | snp | C/T | 0.283158 | 0.247791 | intron-variant | HDAC4 | GRCh38.p7 | 2:239095629 | AGGGCTCCAAGGACG[C/T]TGCAGCTGCACGCCA | 9759 |
rs11695895 | snp | C/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239120422 | acacacacagacaca[C/G]acagatgcacaaata | 9759 |
rs11695950 | snp | A/G | 0.5 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239150627 | CACCTCCTGAAGTAT[A/G]TACCACACCTTCACA | 9759 |
rs11696040 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HDAC4 | GRCh38.p7 | 2:239120735 | TTCTTTAGCAGCCCA[C/G/T]GGGCCATTCTGAAGT | 9759 |
rs11696086 | snp | G/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239120862 | GGAGGGGTTCCTGCA[G/T]CAAATGGCCACTCCC | 9759 |
rs11696099 | snp | C/T | 0.278664 | 0.248351 | intron-variant | HDAC4 | GRCh38.p7 | 2:239297974 | GCGGCTGCTAAGTGC[C/T]TCTGTCCCTACATGG | 9759 |
rs11883563 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | HDAC4 | GRCh38.p7 | 2:239295342 | AAAAAAAGATGATTA[C/T]AGTAAACTGGCAAGG | 9759 |
rs11883623 | snp | C/T | 0.461592 | 0.133149 | intron-variant | HDAC4 | GRCh38.p7 | 2:239295421 | AAAAACCAACGAGAA[C/T]GAGACAAGATGGGAG | 9759 |
rs11883661 | snp | A/C | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239173223 | aaactgtttggcaat[A/C]tccctcaggaacaca | 9759 |
rs11884306 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | HDAC4 | GRCh38.p7 | 2:239067573 | TGAGGATGTGGTGGC[C/T]GCGGTGCTCCGGGCC | 9759 |
rs11884365 | snp | A/G | 0.142947 | 0.22592 | intron-variant | HDAC4 | GRCh38.p7 | 2:239101441 | CTGAGTCTGCCGGGC[A/G]CAGGCCTGGCACGGA | 9759 |
rs11884598 | snp | C/G | 0.3512 | 0.228601 | intron-variant | HDAC4 | GRCh38.p7 | 2:239338914 | GCGTAGGTTCGGTTC[C/G]CCAGTGGCTGAGTTT | 9759 |
rs11885107 | snp | A/G | 0.077417 | 0.180873 | intron-variant | HDAC4 | GRCh38.p7 | 2:239242733 | acgaaggatatttca[A/G]tgttttactggaaag | 9759 |
rs11885793 | snp | C/T | 0.317933 | 0.240593 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239315177 | cacacttcgagttgt[C/T]ccgcgtttctggact | 9759 |
rs11886012 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HDAC4 | GRCh38.p7 | 2:239222838 | AAGCAGGTCCCAGCG[C/G]GGACCTGGGTATCAC | 9759 |
rs11886387 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | HDAC4 | GRCh38.p7 | 2:239247766 | AAAGTGGCCATTTGC[A/C/G]GAAAGTCTAGGCAGG | 9759 |
rs11886812 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | HDAC4, MIR4269 | GRCh38.p7 | 2:239304256 | GCTGGGAAGGCCTCA[A/G]GCAGTGTGAGCTCGG | 9759 |
rs11887902 | snp | C/T | 0.46014 | 0.13543 | intron-variant | HDAC4 | GRCh38.p7 | 2:239243451 | GCCACCGCTCCCGGC[C/T]GGATAAATTAACATT | 9759 |
rs11888868 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | HDAC4 | GRCh38.p7 | 2:239374298 | AACACAGGTCAGAGG[C/T]GCTGCAGGGAAATGA | 9759 |
rs11888915 | snp | C/T | 0.340784 | 0.232934 | intron-variant | HDAC4 | GRCh38.p7 | 2:239168593 | AGAATAAACAGATGC[C/T]GTGCACCGTGTTTTC | 9759 |
rs11889720 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | HDAC4, MIR4269 | GRCh38.p7 | 2:239305200 | TCTGAGGATTGCTGC[A/C/T]GTGTTTTCTAACTGC | 9759 |
rs11891013 | snp | A/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239185851 | gcctggccaacatgg[A/G]aaaaacccatctcta | 9759 |
rs11891124 | snp | A/G | 0.187053 | 0.241946 | intron-variant | HDAC4 | GRCh38.p7 | 2:239246387 | CACCGGGGTTGCTGC[A/G]GGCCACAGGACGCGA | 9759 |
rs11892831 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | HDAC4 | GRCh38.p7 | 2:239056410 | ctgggaaatcaggac[A/G]tgcctgaaggtcaag | 9759 |
rs11894562 | snp | A/C/G | 0.00597678 | 0.0543977 | intron-variant | HDAC4 | GRCh38.p7 | 2:239190295 | CCTCAAGGGCAAAAA[A/C/G]CACAAAAGCCCATGG | 9759 |
rs11894654 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239225458 | CACGAAGGCAGAAGT[C/T]GGTCTGCGGGAGAGT | 9759 |
rs11895350 | snp | A/G | 0.164873 | 0.23506 | intron-variant | HDAC4 | GRCh38.p7 | 2:239134146 | GGGGGTGGGACAGGC[A/G]TGCATTCCTGTCTCC | 9759 |
rs11896634 | snp | C/G | 0.00144656 | 0.026855 | intron-variant | HDAC4 | GRCh38.p7 | 2:239134517 | CACGGACCCACGGGG[C/G]CTGACTTACCGCAGA | 9759 |
rs11897158 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | HDAC4 | GRCh38.p7 | 2:239056454 | acaggacatgcaggg[C/T]cagtctgaaaggtgc | 9759 |
rs11898008 | snp | A/C | 0.0410537 | 0.137264 | intron-variant | HDAC4 | GRCh38.p7 | 2:239258034 | CAATTTAAGATCCTG[A/C]GGCAGTTTTAGAAAT | 9759 |
rs11898644 | snp | A/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239192250 | CCCCACCCCACACAT[A/G]GGTGAGGACTGTTCC | 9759 |
rs11898664 | snp | C/T | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239185697 | GTATCCATGTTTGTG[C/T]CCTGCCTCTCCATAT | 9759 |
rs11899184 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HDAC4 | GRCh38.p7 | 2:239258573 | ATCCTCTAACCAGCA[C/T]GGGCATTCTTCAAAG | 9759 |
rs11899820 | snp | A/G | 0.315516 | 0.241263 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239312797 | GGTGGCCCAGCTGCC[A/G]TGGCGCCGGCAGACT | 9759 |
rs11900589 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | HDAC4 | GRCh38.p7 | 2:239056637 | gagcatttcaaataa[C/T]gcacgtatctactcc | 9759 |
rs11902108 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | HDAC4 | GRCh38.p7 | 2:239143722 | GTGATGCCAATGCTC[A/G]CACACACGGGGCATG | 9759 |
rs11902456 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239311882 | GCCTTGGGCAGCCCA[C/T]GGGGCAGCTCTGAGC | 9759 |
rs11903582 | snp | A/G | 0.475525 | 0.107882 | intron-variant | HDAC4 | GRCh38.p7 | 2:239295291 | CAGCCTGGGTGACAG[A/G]GCAAGACTCCGTCTC | 9759 |
rs11904463 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | HDAC4 | GRCh38.p7 | 2:239368136 | GACAGTCAGCCTGTG[C/T]ATCTCAATCATTGAA | 9759 |
rs12105700 | snp | C/T | 0.0618563 | 0.164627 | intron-variant, nc-transcript-variant | HDAC4, MGC16025 | GRCh38.p7 | 2:239194891 | GCTGGCGCTGATCCG[C/T]CCCTGGCAGTGCTGG | 9759 |
rs12151452 | snp | G/T | 0.147991 | 0.228242 | intron-variant | HDAC4 | GRCh38.p7 | 2:239253344 | ATCTTGAATTAAAAC[G/T]AACACCCCTGTATGC | 9759 |
rs12151480 | snp | A/G | 0.476746 | 0.10529 | intron-variant | HDAC4 | GRCh38.p7 | 2:239254785 | AGTCCTTAGATTTAA[A/G]AAGCATGCTAAGTCT | 9759 |
rs12151485 | snp | A/G | 0.476918 | 0.104919 | intron-variant | HDAC4 | GRCh38.p7 | 2:239255040 | CTAAACTATCATTCG[A/G]GTAAAAGGGAAAACA | 9759 |
rs12151594 | snp | C/T | 0.212425 | 0.24716 | intron-variant | HDAC4 | GRCh38.p7 | 2:239253100 | CATGACATATTTTCA[C/T]CTTCTCCTAAGATAT | 9759 |
rs12232929 | snp | A/C | 0.497091 | 0.0380279 | intron-variant | HDAC4 | GRCh38.p7 | 2:239368309 | GGCCCGCAGAGACAC[A/C]GGAACTTGGCTGTGA | 9759 |
rs12233076 | snp | C/T | 0.277778 | 0.248452 | intron-variant, nc-transcript-variant | HDAC4, MIR4441 | GRCh38.p7 | 2:239085848 | TCTCCTCCCTGTACA[C/T]GAAGGAGACTCTGCT | 9759 |
rs12233096 | snp | A/T | 0.461813 | 0.132798 | intron-variant, downstream-variant-500B | HDAC4, MIR4441 | GRCh38.p7 | 2:239085347 | CCTTCTTGATCTCAA[A/T]TTCCCTTTGTCCGAA | 9759 |
rs12328590 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | HDAC4 | GRCh38.p7 | 2:239284568 | TCAGGTGCCCCTGGG[C/T]ATCCGGTGCCAACAG | 9759 |
rs12373814 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | HDAC4 | GRCh38.p7 | 2:239067424 | CTGATTAGAGAGCCC[A/G]GAACCACGCGCCGCT | 9759 |
rs12463565 | snp | C/G | 0.424037 | 0.179474 | intron-variant | HDAC4 | GRCh38.p7 | 2:239145496 | AAACCTCCGGCGCGA[C/G]GCCCGCCTTGGGAAG | 9759 |
rs12464590 | snp | A/G | 0.0104709 | 0.0715948 | intron-variant | HDAC4 | GRCh38.p7 | 2:239152048 | GAGGGGAAAATTTAA[A/G]AGTCATTATAAAAAA | 9759 |
rs12466124 | snp | C/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239075202 | gcactccagcctggg[C/G]gacagaatgagactc | 9759 |
rs12466878 | snp | A/G | 0.369346 | 0.219673 | intron-variant | HDAC4 | GRCh38.p7 | 2:239099222 | AATTCCACAGGTTTG[A/G]AAGACTGAAGGTGGT | 9759 |
rs12467524 | snp | A/G | 0.134119 | 0.221521 | intron-variant | HDAC4 | GRCh38.p7 | 2:239104778 | GACCCACTGGATAAG[A/G]GACTGAATTGCAGAA | 9759 |
rs12468101 | snp | A/G | 0.138207 | 0.223612 | intron-variant | HDAC4 | GRCh38.p7 | 2:239119644 | AGGGCTGAGGGTGCG[A/G]GGACCAGACCTAAGG | 9759 |
rs12468306 | snp | A/G | 0.153665 | 0.230694 | intron-variant | HDAC4 | GRCh38.p7 | 2:239109428 | ATCCCCAGCCAAGGG[A/G]AGCTGAGATTCAAGG | 9759 |
rs12469994 | snp | A/G | 0.474453 | 0.110094 | intron-variant | HDAC4 | GRCh38.p7 | 2:239132270 | ACACAGAGCATAAGC[A/G]GCTTCCCAGGGTCAT | 9759 |
rs12470591 | snp | A/G | 0.131038 | 0.219882 | intron-variant, upstream-variant-2KB | HDAC4, MIR4441 | GRCh38.p7 | 2:239087134 | GCTGCCTGCATGGAC[A/G]TGGCTCTGTGGCTTG | 9759 |
rs12471054 | snp | C/T | 0.408188 | 0.193589 | intron-variant | HDAC4 | GRCh38.p7 | 2:239360513 | TGTGACTCATGTGCT[C/T]GCTTATCTGATGAGC | 9759 |
rs12471350 | snp | A/G | 0.172997 | 0.237846 | intron-variant | HDAC4 | GRCh38.p7 | 2:239157903 | GTGGGGTGCTGGGCC[A/G]TGCATCACAGGAGGA | 9759 |
rs12472107 | snp | A/C | 0.313082 | 0.241911 | intron-variant | HDAC4 | GRCh38.p7 | 2:239060396 | ATCTGTCTAATTCAC[A/C]CCACTAAGAACAAAT | 9759 |
rs12472108 | snp | C/G | 0.313082 | 0.241911 | intron-variant | HDAC4 | GRCh38.p7 | 2:239060397 | TCTGTCTAATTCACC[C/G]CACTAAGAACAAATA | 9759 |
rs12472246 | snp | C/T | 0.124144 | 0.21601 | intron-variant | HDAC4 | GRCh38.p7 | 2:239090888 | ATGTAAGGGGAATCA[C/T]GACCAGTCTCTTCCA | 9759 |
rs12475311 | snp | A/G | 0 | 0 | intron-variant | HDAC4 | GRCh38.p7 | 2:239142082 | GAGTGAGAGAACTCA[A/G]GTGTGAGGAAGGCAC | 9759 |
rs12475580 | snp | C/T | 0.351853 | 0.228311 | intron-variant | HDAC4 | GRCh38.p7 | 2:239334343 | tgatcaacatggtga[C/T]gccccgtctctacaa | 9759 |
rs12476417 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | HDAC4 | GRCh38.p7 | 2:239290006 | AAAATTAACAAAGTT[A/C]TATCAACTACAGAAA | 9759 |
rs12476461 | snp | C/T | 0.46885 | 0.12085 | intron-variant | HDAC4 | GRCh38.p7 | 2:239370711 | GGTGCACCTGCAGCC[C/T]TGCGGCGCCTGGAGG | 9759 |
rs12476996 | snp | C/T | 0.442957 | 0.20933 | intron-variant | HDAC4 | GRCh38.p7 | 2:239336199 | CTAGAGAAGTGGTAT[C/T]TAGAGGGTGTGAGAG | 9759 |
rs12477189 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | HDAC4 | GRCh38.p7 | 2:239158210 | TCTTTCTCTACCAAA[C/T]AGTATTTTCAGATTG | 9759 |
rs12477294 | snp | C/T | 0.225893 | 0.248835 | intron-variant | HDAC4 | GRCh38.p7 | 2:239296238 | ACATATGCAGGTATG[C/T]ACACATGCACGCACA | 9759 |
rs12477532 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | HDAC4 | GRCh38.p7 | 2:239371646 | TCATATAACCTCAAA[A/C]ACACATACGCACGGA | 9759 |
rs12478301 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HDAC4 | GRCh38.p7 | 2:239340093 | ACACATTCAGGCCAG[A/G]ATGGTCCCTGCAGCA | 9759 |
rs12478915 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | HDAC4 | GRCh38.p7 | 2:239313115 | TGTCCCGTGCCTCCC[C/G/T]GGGGGCGTTCCGAGG | 9759 |
rs12613718 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HDAC4 | GRCh38.p7 | 2:239378608 | GAGGTGGCCTGAAAC[A/G]GCCCCGGGAACCAAG | 9759 |
rs12613816 | snp | A/T | 0.306927 | 0.243432 | intron-variant | HDAC4 | GRCh38.p7 | 2:239198113 | ggcctcccaaagtgc[A/T]gggattacaggcctg | 9759 |
rs12614834 | snp | C/G | | | intron-variant | HDAC4 | GRCh38.p7 | 2:239279566 | GGACACTGTCGGGGT[C/G]AGGAGCAGAAGGGCA | 9759 |
rs12615371 | snp | A/G | 0.400147 | 0.19989 | intron-variant | HDAC4 | GRCh38.p7 | 2:239260970 | CACTGGGGTGGAGAC[A/G]GAAGCCAGCCTGGGA | 9759 |
rs12615955 | snp | A/C | 0.338523 | 0.233803 | intron-variant | HDAC4 | GRCh38.p7 | 2:239276543 | TCACCAGTCATGGGG[A/C]CCTAAGTCCCTCTAG | 9759 |
rs12617027 | snp | A/G | 0.336017 | 0.234736 | intron-variant | HDAC4 | GRCh38.p7 | 2:239152888 | CCTCGATCTGGTCCT[A/G]CTCGAAGGACTTTGC | 9759 |
rs12617218 | snp | A/G | 0.49917 | 0.0203505 | intron-variant | HDAC4 | GRCh38.p7 | 2:239388087 | AACATGGCAGGACGC[A/G]GCTGGGCAGGTCCTC | 9759 |