Tag | Content |
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EnhancerAtlas ID | HS092-12788 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:88825080-88830040 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6 | MA0463.2 | chr12:88829225-88829241 | ATTTCCTGGAAAGCCC | - | 6.15 | E2F3 | MA0469.3 | chr12:88826736-88826752 | ATTTTGGTGCCAAATT | + | 6.01 | E2F3 | MA0469.3 | chr12:88826736-88826752 | ATTTTGGTGCCAAATT | - | 6.02 | GATA2 | MA0036.3 | chr12:88828692-88828703 | ACAGATAAGAA | - | 6.14 | Gata1 | MA0035.3 | chr12:88828692-88828703 | ACAGATAAGAA | - | 6.62 | HNF1A | MA0046.2 | chr12:88825269-88825284 | AGTTAATCATTTACT | + | 6.74 | HNF1A | MA0046.2 | chr12:88825269-88825284 | AGTTAATCATTTACT | - | 6.96 | HNF1B | MA0153.2 | chr12:88825270-88825283 | GTTAATCATTTAC | + | 6.39 | HNF1B | MA0153.2 | chr12:88825270-88825283 | GTTAATCATTTAC | - | 6.87 | MIXL1 | MA0662.1 | chr12:88829164-88829174 | TCTAATTAAC | + | 6.02 | MYB | MA0100.3 | chr12:88829814-88829824 | GACAGTTGGT | - | 6.02 | Myod1 | MA0499.1 | chr12:88825487-88825500 | TGCAGCTGTCTCT | + | 6.36 | Myog | MA0500.1 | chr12:88825486-88825497 | CTGCAGCTGTC | - | 6.62 | NFAT5 | MA0606.1 | chr12:88826942-88826952 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr12:88826942-88826952 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr12:88826942-88826952 | AATGGAAAAT | - | 6.02 | REST | MA0138.2 | chr12:88826994-88827015 | GCTGCTGACCTTGCTGCTGAC | - | 6.24 | SOX10 | MA0442.2 | chr12:88829785-88829796 | AAAACAAAGCA | + | 6.02 | STAT1 | MA0137.3 | chr12:88829226-88829237 | TTTCCTGGAAA | - | 6.62 | Stat4 | MA0518.1 | chr12:88829223-88829237 | CCATTTCCTGGAAA | - | 8.42 | Tcf12 | MA0521.1 | chr12:88825486-88825497 | CTGCAGCTGTC | - | 6.14 | ZBTB18 | MA0698.1 | chr12:88825424-88825437 | AAACATCTGGAAG | - | 6.46 | Zfx | MA0146.2 | chr12:88828752-88828766 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH12I088432 | chr12 | 88826285 | 88827190 | GH12I088433 | chr12 | 88827374 | 88829755 |
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Enhancer Sequence | ACTTCTGTTT GGAAATTCAA TTCTAACTAG CGACTTCTGT TACTGTAGCT ATCCTGTACA 60 TGGCAGTCAC TGTATGTGGC CAGTGACACT CTGCATACAT GCTGAGGGCT ATAATAGTGG 120 TAAGAAGGGT GGCAGGAAGA AACCTAGTAA TATGGTCAAG GACTGTCTGC TCCCTAGTGG 180 CAGCAGAAAA GTTAATCATT TACTTAACTT TAACTGTTAC TAGCAACAGA TTAATTACGA 240 TGTATTGGAA AGTAATTGGT ATCCACCATA GTGCCTTGTT GCCACAGTGA GCTGCTGCCT 300 GTGACACTGG AGCTGCTTGT TACCAAACAC AGGCAGAGAT ATGGAAACAT CTGGAAGGTC 360 CCTGAGGTAC CATAGCTATT GAGGTGGCCC TGGTTATCTC TGGAAGCTGC AGCTGTCTCT 420 TGATTCAGTC TAGAAAAACC GAAGTCCATG AGACAACAGG TTATCAGTTG AGTTTCGGCT 480 CTGTTATGAA CAACTCCATG GAACAATTTC TGAGTATTAG AGACGTAAAC ATCTTCCTGC 540 ATCTTCCTTT TATGGTGATT ATCTCCTCTG CTAGTCCAGG AGCCTTTTGA GCAGTGGGAC 600 TTACTTACAC CTTGACATTC CCTATAGACC CTCGCAGAAT CTTAAAGGAA GCTGCTACAG 660 ACACCACCAC CACTATATAT GAAGAAACTA TCCCAGACAC TGCTCCAGGG GCTCCACAAT 720 CATAATTCTA TTTAATCCTC ATAGGCCACT CTAAGTTATA TATTGCTTTC CTATTGATGG 780 ATAGAATGAT TGAAGTTCTA AGTAGTTGTA AGGTTTGTGC AAGGGCACAA AGCATGGGGC 840 CAACATTCTA CCCAAACCTG TGTTACTCTC ACACCTTATT TTCTGTCACT GCAATAAAAT 900 ATCTCCTTCA CATAACACCT CTCAGTGGTG GCTGTTTCTG AGCTTGTCTG CTTGCACTGT 960 ATCCATACAC AAACCTGGTG GTTAGACTGT CTTTGGAGGG AATTTGAACA CAAGAGAGTA 1020 GAAACAAGAT TTGTGGCTAT CAAGATAATA GAGGCAAGTA GTATTACCAA ATATACAGTC 1080 CATTGCTTTA GAAATTTTGC AAAGAACAGT CAATAATAAT TAGTTTTTAC ATACATCTAG 1140 TGAAAATATG ATAAAATGTT GTTCAAAATT TTATAGCTAG AGGTGAAAAG AATTCAGAGG 1200 AAGTTGTCTG AGTATTCCTA ATGCTTTCAA TCTACAGCAG CCAAAGCCAT ATTTATTGTT 1260 TTCATAGAAA GTAAGAAGTT TGGGATCATA GTTACTAACT TTGGTCTGGA ACTTCTGGCC 1320 TACGGCCTGT GTTTTAGAAC TGCTAGATTG CATTGTACTC CAAAGAGGCA TGTGACCAGT 1380 GAGCAAAACC AGATGGTGAA GTATGCAAGG CCTATCTTCT GCTGAACTCA CTTCTCTCTT 1440 ATGAAGCCCT CTGACCTCCC TGCCTGCCCC AGTTCTCAGT GCTCCGCTCC ACACATCCAG 1500 GAGAAAACAA ATCATTAGTG TTTTCAGAAA AATTTGTCTG TTAGACGTCT CTGAGACTTT 1560 ATAACTACCC CAAAGGCAGA AACTCAAAAT AATCTTTGGT GATACCGATG ACTAATAGTG 1620 GTATTTCAAC TTCTGTGTCT TCTGATTAAG GGAATTATTT TGGTGCCAAA TTATACTCTG 1680 TAAGGGGCAA ATTGTATTAC TAAATCTGCC ACTTGCCCTC TCCTCTCAGG TGGCTTTGCT 1740 TAGCACTACA AAGATGGTAG AAAAACAGTT TTCCAGTAGC CACATAAGAG ACTATGCACA 1800 ATTCCAGATT TGATTCCACA CTAATATAGA GGTGGAAGAG TTGCTAATAG TAGAGCTCGA 1860 TGAATGGAAA ATTGCAAGCT GGTTTTTCGT TTAGGATGGG CTGCTGTTGA CCTCGCTGCT 1920 GACCTTGCTG CTGACCTCAC TGCTGACCTT GCTGCTGACT TCACCGTTTC TCCCAATATA 1980 TGTCAGCTGA GTGGACTTTT GGCTGCCGGA CATGAAGAAA TCATATAATC AATTAAGCAA 2040 TCAATCAACA AATATATAGT GGACTTCTGC AATTTGCAAG GCTCTGTGGC AAATTGTACA 2100 AGGTATGCAA AGATGACTTA TAAGCAATAT TCCTGTTTTT AAGTAGTATG TGACAACTAC 2160 CAAATGAAGA GTGTACATGA TATATATTAC AGGAGTCAGA GGAGAAAGCT ACTCCTGTGG 2220 CTGAAGTTCT AGAGAAAGTT TTGTTTTTTA GCAGCATTTG CCATATAGAG TAATATTATA 2280 GGAAAATAAC ATAATTTTTA AACTGAATAC TTTCTTCATG CCAGGCACTG TGTTAAGCTG 2340 TTTACACAAA TAGTATGCGG AATACTTAGA TGAGTACATG GCACGTGGTA AATGCTCAAT 2400 AAGTATTACT TTTTGTTTTT AATCATTGCA TTAATCCTTC CATACCCTTT TAGTAGGAGC 2460 TATTATTTCC CACATACTAT AGTTGACAAA ATGGAGGCAA ATTAAGGTTA TATGACTTGT 2520 ATAAGCTAGT AAGTGTGAAC ATAGATACTG ACTCCAGAGT CAATAAGGTT GGTAAGTAAG 2580 GCAGAAGCTG GGGGCTGGGG TTGGGGTTTA CACCCAAGGA GCACCAGGGG CATATGAATA 2640 GAAGTCATAA CGTTCTAATC CTGTTCAGGA GGTCAGAAAG TTAACTAGGG TAGAGAACAG 2700 GATGAAAAGC TATGAGAGGT CTGCCTAGAA AAATAATTGA GAATGAATTA TGATGGATTT 2760 CAATATTGAC TGGGAAGGAT ATTTTCAAAA TCTGCTTATC TTACACGTAG TAGAGAGCCG 2820 ATGGTATTTA TACACACACA CGCACCTGTG TGCAGGCACA TGCGCTGACA TAAAGGAAAG 2880 GACGTTTTTG TGAAGATTAA GCTAGGGATA TTATCAGAGC TAAGTTATCC ATTAAGCACA 2940 GTAGGCACAG TCTCTAGAGC CCAAAGTACA TTTAGCACAT TTCAAATGTT TTATAATATT 3000 TTAAGTGAGA AGGACAAATG AATATAATCG TAATAATTAA TACTTAATAA TGAATACAGA 3060 CTAGATTATG TTTATCTTTA TAGCAATAGA ATCATAAAAT CTAATTTTTA ATTTTTTTCC 3120 TGGACAGGGG AAAAGTGTTT GTGGCCCACA GAAATCATGC TGCAGCCCTG GGTGATATGC 3180 TGAGACATCT GGGGGAGGAA ATGACTAGGC ATAAGTAAAA CAGGGAACTA CTAAAATCCT 3240 TATGCATGCA GGCTTTGACT AAGTTTGTGA CCATGACAGT GTAAAATGAA AGCCAAAAGC 3300 ACTGCAAATA AAAAGCGTAG AAAAGTTAAC TGCCTCTGTA TGTATGGGCG TTTGGTGGAA 3360 TGTGAGATTA TGAGTTACAT CTGGGGACAC AAAATGTAAA TTTGATTCAA GATAGTGGGC 3420 AACTATATGC ATTTACTTTC TTTGCATTTC AATGAGGCAG GCAGTTAGCA AATGGGCATG 3480 ATTATTTGCA GGCGGCTAAA AGCAATACAA GTGGGCCTAG ACAGGTTAGC ATAAGGACCC 3540 ATCTCCCCAG TAGGAAGAAA CTGTTACAAC AGACTATAAC AATGAAGAGA TTGCAGACAT 3600 CCTGCTTTAG GCACAGATAA GAATATAACA GGCCGGGCGC GGTGGCTCAC GCCTGCAATC 3660 CCAGCACTTT GAGAGGCCGA GGCGGGCGGA TCACGAGGTC AGGAGATCGA GACCATCCCG 3720 GCTAAAACGG TGAAACCCCG TCTCTACTAA AAATACAAAA AATTAGCCGG GCATAGTGGC 3780 GGGCGCCTGT AGTCCCAGCT ACTTGGGAGG CTGAGGCAGG AGAATGGCGT GAACCCGGGA 3840 GGCGGAGCTT GCAGTGAGCC GAGATCCCGC CACTGCACTC CAGCCTGGGC GACAGAGAGA 3900 GACTCCGTCT CAAAAAAAAA AAAAAAAAAG AATATAACAA AAAATAAACT GGGTGGCAAC 3960 TGGTTAAATC CAAGGTGACC GAAAATTACT CACTGTTGAT CCTTGGCTTC ACTATGCCCC 4020 ATTACCATAA CATTTCTGTG GGGAAGCCTC CCACTCCTAT CATGCACCTG ATGCCATGAC 4080 ACTTTCTAAT TAACCATATT TAGTTAAGAA AAGGGTGGTA CCCCCATTCC AGGTGTTGCT 4140 CACCCATTTC CTGGAAAGCC CCTCCCCTAA TTATAGAATA TTCTGTGCCT TCATCATGCT 4200 TATCCATATA ATACATGAGC CCTGACCACA TGGCATGCGG CTCATTCTTT TGAGCATGCA 4260 TGCACTCCTC TCTTGAGTGT GTACTTGCTT TCACTCTGCA ATAGAGTTTC TATACTTTCA 4320 CTGTGGTCTT GCTTCCAAAT TATTTTGTGT GGTGAACACA AGAAACTGAA ATAGACTTCT 4380 GGAAGCACCA ACATTTCTTG AAACAACAGA AGAGATATAT TTTTCAAAAT CTACCATACT 4440 GCTTAAAAGT AAAAGGCTGA AGCAGCAGAC TAGAGAAAGT TCAGGACTCT GACTGACAAA 4500 GAAAAAATCA AAGCTGAGAA ACCTGAAATA AGCACAGGGA GAGTTGCAGA ATTCATGTCA 4560 GACTAAAGGA GCCTAAGAAT AGAAACTCGT CATAGGACGA GGAGTGTAAT AATTCGTTTA 4620 AAGGATTGTG GAAAACTAGA TCAGTTCTAT GTAGGGCAGC TGGCTGAAAT GTTTGCCTCT 4680 GAGTATAAAC CTAATGATAG CTTTCAAAAC AAAGCAGAAA ATCTGCTGGG CTAAGACAGT 4740 TGGTAAAATC TCAACATGAC CTTGGTGCTA AAAACAAAAT GATGCAGATC CTGGGTGACT 4800 TTAAACCCAC ACAGATATGG AATAAGGGCG GGAGAGAATA AATGGCTCAA CACTGCAGTG 4860 AAATACACTG TAATGTTCTA TTTCCTTTCA TATCTCAGCA TATGAGAGAA GTCCTGCCTT 4920 CCTTGCCAGC TTTCTGCCCA TGAGCCCATC AGCCAGCATA 4960
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