Tag | Content |
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EnhancerAtlas ID | HS104-03858 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:155016960-155017660 |
Target genes | Number: 34 | 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 | AAAAAAAAAA AAAAAAAAAG CTAATGATCT AGTTGGGATC ATGAGACACC CACAAGACAG 60 AGATGGTTCA AGGGCCATTC TATGGATTGG CTTTTGAGAC GTGTATGGGA GCTGGGAAGG 120 TGCCCCTTGG AAGGGCAATA ACTGGGCTCC AAATGGCCGC AGATGCGGAA CGGTGGTCAA 180 GGAAAGAAGG GTGTCCCTTG CGTAAGGCTC CTGGTATCCA TGGGATGCAG AGGGCAGAGG 240 CTGGCCTGGA GAACTGAAGT GGGCATGACC AGAACAGTCT GGAAAGCCCT GCAGGAAGAC 300 CTGGAACTGG CGGTGGTGGC AAGATGGCCT CAGGAAGTCT GGAGGGAGGG CGGGAGGCCA 360 GGCTGGGTTG GAGGTTAGGG AGCCTGGCCC GGGTAGAGCA TGGCAGGAAG ATGGCTTGAG 420 ATGGTGGGGG AAGGGGAAAG GTGCAGCGAG GCTCAGAGCC AGCTTGTGGA GGGAAGGAAG 480 GAGGCACAGA GTCAAAAGCT ACTTCCAGGC TTTCAAGCTG GGTGAGGTCA TGCACTGAAA 540 GGACAGCTGG CGGGAGGGCA GGCCCTGGCT CAGGAAGCCC AGGCACCACC TCTGTGAGCC 600 TCTCCACAAG AGGGCACTCA CAGTATGTCT TTGCACTTAC AGTAGTTTTA AAGGCAAAGA 660 TGTGGATTTT TACAGGGCCC CAGAAGCAAT AGCATTGAAA 700
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