Tag | Content |
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EnhancerAtlas ID | HS051-01466 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr1:149764120-149764780 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:149764606-149764625 | CGGCGCCACCTGGCGGCCG | - | 7.17 |
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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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Enhancer Sequence | GGATGGGGCG TCGCGCTCCG AGCGTGTCCC GCGGCGGGCC CCTGGCGCCA CACTGTGGCC 60 GCATGTGCAT ATTGCAGCCT CCGCCTGTAT CTGGGGGCCG CAGCCGCCAG CGCCCGGGGA 120 CCCAGCTGCG GCGAAAGCTG TTGGGCGCGC GCTTCTCCGC AGCTCCGCGC CCCCGCCAAA 180 ACCCAGTGAG AAATTATTTG CATTCCTGGA GGCTGCAGGA GCGAGAAATG AGCTGTAGGA 240 GTCGGTGGGC AGCAACGGCG GCAGGCGGAT GGAAGAGAGC AAGGGGTCGC CGTTCGTGTC 300 CCATTCGCCC GAGTCAAGGG GCGGCCCCCC AAAATCCCAA CGTCATTGTT TCCTCGGGGC 360 CGGCAGGTGT GAAAACCCGG CGGCAGAATG GAAGTTCGGT AGTCTGCGAG GGCCCGCGGC 420 CTCCCCAGGC GCGTAGCTGA GTCCCTCCAA CCCCGCCCCG GGCCCGCCAG CTCCCGGGCC 480 CCGGCGCGGC GCCACCTGGC GGCCGTCTGT GGAGGTTGCA GCTGCCGCCA AGCCCCGGGG 540 ATGCTGCCGG CCTCAGGTGC GCCCGGCCGA GCCTCCGCGG AGAGGAGGAT TGGTAGATCA 600 CAGGAAACGG GAGGACGGCG CTGGGCTCCC AGCAGGCGCC CCATTTTCTT GGCTTGTCGC 660
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