Tag | Content |
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EnhancerAtlas ID | HS098-03537 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:155017000-155017660 |
Target genes | Number: 32 | 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 | ATGAGACACC CACAAGACAG AGATGGTTCA AGGGCCATTC TATGGATTGG CTTTTGAGAC 60 GTGTATGGGA GCTGGGAAGG TGCCCCTTGG AAGGGCAATA ACTGGGCTCC AAATGGCCGC 120 AGATGCGGAA CGGTGGTCAA GGAAAGAAGG GTGTCCCTTG CGTAAGGCTC CTGGTATCCA 180 TGGGATGCAG AGGGCAGAGG CTGGCCTGGA GAACTGAAGT GGGCATGACC AGAACAGTCT 240 GGAAAGCCCT GCAGGAAGAC CTGGAACTGG CGGTGGTGGC AAGATGGCCT CAGGAAGTCT 300 GGAGGGAGGG CGGGAGGCCA GGCTGGGTTG GAGGTTAGGG AGCCTGGCCC GGGTAGAGCA 360 TGGCAGGAAG ATGGCTTGAG ATGGTGGGGG AAGGGGAAAG GTGCAGCGAG GCTCAGAGCC 420 AGCTTGTGGA GGGAAGGAAG GAGGCACAGA GTCAAAAGCT ACTTCCAGGC TTTCAAGCTG 480 GGTGAGGTCA TGCACTGAAA GGACAGCTGG CGGGAGGGCA GGCCCTGGCT CAGGAAGCCC 540 AGGCACCACC TCTGTGAGCC TCTCCACAAG AGGGCACTCA CAGTATGTCT TTGCACTTAC 600 AGTAGTTTTA AAGGCAAAGA TGTGGATTTT TACAGGGCCC CAGAAGCAAT AGCATTGAAA 660
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