Tag | Content |
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EnhancerAtlas ID | HS127-26709 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr6:33475850-33477980 |
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) |
HOXA13 | MA0650.2 | chr6:33476635-33476646 | ACCAATAAAAC | + | 6.32 | MEF2A | MA0052.3 | chr6:33476495-33476507 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr6:33476495-33476507 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr6:33476494-33476509 | TTCTATTTTTAGTAG | - | 6.57 | Nr2f6(var.2) | MA0728.1 | chr6:33477916-33477931 | GAGTTCAAGAGTTCA | + | 6.19 | Nr2f6(var.2) | MA0728.1 | chr6:33476000-33476015 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr6 | 33477400 | 33477755 | chr6 | 33476217 | 33476331 | chr6 | 33475884 | 33477400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I033508 | chr6 | 33476578 | 33477577 |
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Enhancer Sequence | AGTGCTGGGA TTACAGACGT GAGCCACTGG GCCCTGTCTA AAATATATTT CTTACTGTGG 60 GTCCTAGTCA AAAAAGTTTG AAAGCAGGCC AGGCACGGCT CACGCCTGTA ATCCCAGCAC 120 TTTGGGAGGC CCAAGGTGGG TGGATTACCT GAGGTCAGGA GTTCAGGACC AGCCTGACCA 180 ACATGGTGAA ACCCCATCTT TACTAAGTAC AAAAAATTAG CTGGGTGTGG TGGCACATGC 240 CTGTAATCCC AGTTATTTAG GAGGCTGAGG CAGGAGAATC GCCTGAACCC GGGAGGCGGA 300 GGGTGCAGTG AGCCGAGATT GCACCATTGC ACTCCAGCCT AGGCAACAGG AGCAAAATCT 360 GTCTCAAAAA CAAACAAAGA AACAAAGTTT GAAATTAACC GACATAGTGA CTAAATTCGT 420 ACCCTTTTGA GTCAGCTGGA ACTGGGCTCA GCTATGTGGC TTCGGGCAAG TAACTTAACT 480 TCTTTTTTTT TGAGACAGAG TTTCGCTCTT GTTGCCCAGG CTGGAGTGCA AGGGCGCGAC 540 CTCGGCTCAC CACAACCTCC GCTTCCGGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCG 600 AGTAGCTGGG ATTACAGGCA TGTGCCACCA TGCTTGGCTA ATTTTTCTAT TTTTAGTAGT 660 GACGGGGTTT CTCCATGTTG GTCAGGCTAG TCTCAAACTC CCGACCTCAG GTGATCTGCC 720 CGTCTCGGCC TCCCAAAGTG CTGGGATTAC AGGTGTGGTA ACAACTTCTC TGAGAGAATT 780 TCCTCACCAA TAAAACAAGA TTGTAATATC CGTCTTCTTA GATTGTTATA TGAGGATTAA 840 ATAAGTGCAA ATTGCTTAGT TCGGCATCGG GAATGTAATA TGTTCAGAAG ATGTGGTTAT 900 TATTTTCTAG CTTTAAAGAT ACGCACACAT GGCCTTGTTT CTTTCTCATT CCCAGCTCTA 960 TTAATTTCAC TTCCTACTTT CTATTTTCAG CCATTTAGAG AAGCAAGTCT GCGACTCTCT 1020 AGCAATCCTG GATTTTATGG AAATTATCTC TCCCATCTCA GAGGGTTTCA AGGCCCATAA 1080 ACCTGCTCCT CCCACAGCTT GCTGTCTGCA GTTCGGGGGC GGATGAACCA CTCTGTGTCC 1140 CAGCCCACTC TCCGCTGTTG AGGATCAGCG TCCCGGGATC TTTGGTAATA GAGGATGCAG 1200 CTGAGGGTTT TGTTTTTAAA ACTGGGCTCT CCTTCCTTTT CCTCTGAGGA AAGGAAACTT 1260 TTTTCCTGCC TCTCCTCCCA ACATTGCAAG CTCTTCCTCG CTTTCTCTCA CAGGTCTGCG 1320 CTCTCCTGCT AAGCCCAGGA CGTTTCCTTC CCTTTTTCCC TGTGCCCCTG TTCCTTGGCC 1380 ACAGGGTGGA GGTGAGCTCA CGCCCCTGCC CCTCCGTTCC CTTCACCTCC ATTCTGGCAT 1440 GTTGCCCCCA CTGTTCTCAG ACTGGGGTGC TCGAGCAATC TGCCCTCCTG TGTTTTGGGG 1500 GCTGTCCAGC TGTAACCCCT TCCCTGGGTT GGGCTGCTTT ACACTTGGGC TCCCACCAGG 1560 GTCCAGGAAG GGGTGGGGGC TTGGGGGTGG AGACTATGGA CCCCACCTCC TCCTGGGAAT 1620 GGGCACCTGG ATGGCTGCTT TATGGCCATG TGAAAGCAGA GCAGGCATCA CTCATTCCAT 1680 CCTCATTCAT TCCTTCACTC ACAACAAGTG CTGCAGATAC CCAAGATGAC TAAGAAATGG 1740 CCCCTGCTTT CAAAAAGCTC AGTCTAGTCC CATGATGTCC TTAATCACAC CCCCTCAAAA 1800 AAGTCGTATT AAGCAGTAGG TAAGGGGAAG TGACCTCTAA GAAGGATCTA ACAGTGGAAA 1860 TTACCTATCT TAACGACACA GGTAAATTCA ACTTTGTAAA AGAGTTTATG GAGTGAGAAA 1920 AAGCATCAGA ATCAAGTAAG TTTGAGGGAT GAAGCCAAGT GTGCTTTTAG AAAAGTCTAT 1980 TCACATTGCA AAGGTTTCTC TCCTTTCGAC AGTGGCTCAT GCCTATAATC CCAGCACTTT 2040 GGGAGGCCAA GGTGGGAGGA TCACTTGAGT TCAAGAGTTC AAGACCAGCC TGGGCAACAT 2100 AGGGAGAACC TGTCTCCATA AAAAGGTTTA 2130
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