Tag | Content |
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EnhancerAtlas ID | HS127-26597 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr6:29931510-29932890 |
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) |
DUX4 | MA0468.1 | chr6:29932191-29932202 | TAATTCAATCA | + | 6.14 | FOXP1 | MA0481.2 | chr6:29932208-29932220 | TTCTGTTTACTG | - | 6.02 | NFE2L1 | MA0089.2 | chr6:29932792-29932807 | ACTGCTGAGTCATTT | - | 7.29 | Nfe2l2 | MA0150.2 | chr6:29932794-29932809 | TGCTGAGTCATTTCC | - | 6.41 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_57150 | chr6:29932125-29934802 | VACO_400 |
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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: 1 | ID | Chromosome | Start | End |
GH06I029963 | chr6 | 29931647 | 29936405 |
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Enhancer Sequence | AAAGGATTAT AAACATTTTA CTATAAAGAT ACATACACAC ATATGTTTAT TGCGGCACTG 60 TTCACAATAG CAAAGACTTG GAACCAATCC AAATGCCCAT CAATGATAGA CTGAATAAAG 120 AAAATGTGGC ACATATACAC CATGGAATAC TATGCAGCCA TAAAAAGGAT GAGTTCATGT 180 CCTTTGCAGG GACATGGATG AAGCTGGAAA CCATCATTCT CAGGAAACCA TCAGCTACGT 240 GTTCTCTGGG TCTCTCAGAG AAAGACCCAC AAGAACAGAA AACCAAACAC TGCATGTTCT 300 CACTCAAATG GGAGTTGAAC AATGAGAACA CATGGACACA GGGAGGGGAA CATCACACAC 360 TGGGGCCTGT CTGAGGGTAG GGGGCTAGGG GAGGGATAGC ATTAGGAGAA ATACCTAATG 420 TAGATGATGA GTTGATGGGT GCAGCAAACC ACCATGGCAC ATGTATACCT ATGTAACAAA 480 CCTGCATGTT CTGCACGTGT ATCCCAGAGT TTAAAGTATA ATAATGATAA TAATAATAAA 540 TTGGATTTGT AAGTGTGCCT TTAACAAGTA CTGAGGTTAG GAATTTTAAA AAGGAAATGA 600 GGCCACTCTC GGAAGATCCC CTCAGTTTAG CAGAACAGCT AGATCAATTT TTAGAACCAA 660 ATTTTTATAC TTGGGCTGAG ATAATTCAAT CATGAATATT CTGTTTACTG GGAAAAAGAC 720 GGGAATAATT AGAAGGGCAG CCATAATCAT TTGGGAGAGA CAGCAGCATC CTCCTGGGTA 780 AGGAGTCCTG CCAGCTAAGC AGAAATTCCC AAATGCAGAT CCTGGATGGG ATAATAATGA 840 CCCCAGGGAT CGGGTCCAAA TGCAAGACCA TAGGGAGCTA ATAATTAGAG GGATTATGCA 900 GTCCACTCAT AGGACACAAA ACGTCCCCAA AGCATTCAAG ATCCAACAAC AAGAAGAGGA 960 GACTCCCTCT GCATTTCTGC AGAGGCTCAG GGATCAAGTG AAAAAATATT CAGGATTAAA 1020 TCCAGAGGAC CCAGTAGGGC AAGGCCTTTT AAAGGTTAAT TTTGTAACTA AAAGCTGATG 1080 TAATATTACT AAGAAACTGC AAAAGATTAA CGGATGGAAT AAAAAACCAA TTAAGGAAAT 1140 ACTGAGGGAA GCTCAGAAAG TTTGTGTGTG TGTGTGAGAG AAAGAGAGAG AGAGAGAGTT 1200 AAGCTGCTAT ACCTGAAGGA AGAGAGAGCC AGCGGCACAG CTGTGTGTGG CAGCTGGCTT 1260 CTAAAAGCTG TTGATAAAGG TTACTGCTGA GTCATTTCCG CAGAGCTGCC TGTTTTTGCA 1320 GACAGACAAG GGGAGCCAGG GCACAGCACG GCTCGGCTCA TGCCCAGAGA AAGAGGAAGA 1380
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