Tag | Content |
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EnhancerAtlas ID | HS006-02408 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr1:155017030-155017660 |
Target genes | Number: 29 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:155017560-155017579 | TCTCCACAAGAGGGCACTC | + | 6.44 | EWSR1-FLI1 | MA0149.1 | chr1:155017431-155017449 | GGAAGGAAGGAGGCACAG | + | 6.04 | EWSR1-FLI1 | MA0149.1 | chr1:155017427-155017445 | GGAGGGAAGGAAGGAGGC | + | 7.41 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27386 | chr1:155016985-155017672 | Esophagus | SE_41765 | chr1:155016859-155017626 | LNCaP | SE_50747 | chr1:155015129-155018108 | Sigmoid_Colon |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I155042 | chr1 | 155015098 | 155018110 |
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Enhancer Sequence | AGGGCCATTC TATGGATTGG CTTTTGAGAC GTGTATGGGA GCTGGGAAGG TGCCCCTTGG 60 AAGGGCAATA ACTGGGCTCC AAATGGCCGC AGATGCGGAA CGGTGGTCAA GGAAAGAAGG 120 GTGTCCCTTG CGTAAGGCTC CTGGTATCCA TGGGATGCAG AGGGCAGAGG CTGGCCTGGA 180 GAACTGAAGT GGGCATGACC AGAACAGTCT GGAAAGCCCT GCAGGAAGAC CTGGAACTGG 240 CGGTGGTGGC AAGATGGCCT CAGGAAGTCT GGAGGGAGGG CGGGAGGCCA GGCTGGGTTG 300 GAGGTTAGGG AGCCTGGCCC GGGTAGAGCA TGGCAGGAAG ATGGCTTGAG ATGGTGGGGG 360 AAGGGGAAAG GTGCAGCGAG GCTCAGAGCC AGCTTGTGGA GGGAAGGAAG GAGGCACAGA 420 GTCAAAAGCT ACTTCCAGGC TTTCAAGCTG GGTGAGGTCA TGCACTGAAA GGACAGCTGG 480 CGGGAGGGCA GGCCCTGGCT CAGGAAGCCC AGGCACCACC TCTGTGAGCC TCTCCACAAG 540 AGGGCACTCA CAGTATGTCT TTGCACTTAC AGTAGTTTTA AAGGCAAAGA TGTGGATTTT 600 TACAGGGCCC CAGAAGCAAT AGCATTGAAA 630
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