Tag | Content |
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EnhancerAtlas ID | HS052-15245 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr17:1480310-1481540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr17:1481439-1481454 | GGGACAGGCTGACCC | - | 6.32 | SPI1 | MA0080.4 | chr17:1481159-1481173 | AACTTCCGCATTTA | - | 6.42 | SPIB | MA0081.2 | chr17:1481159-1481171 | AACTTCCGCATT | - | 6.27 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_09501 | chr17:1477198-1482172 | CD14 | SE_24303 | chr17:1480428-1481001 | Colon_Crypt_2 | SE_24303 | chr17:1481005-1481629 | Colon_Crypt_2 | SE_25267 | chr17:1480380-1481766 | Colon_Crypt_3 | SE_27390 | chr17:1480364-1481857 | Esophagus | SE_41871 | chr17:1480390-1481757 | LNCaP | SE_50860 | chr17:1480343-1481848 | Sigmoid_Colon | SE_53184 | chr17:1480354-1481865 | Small_Intestine | SE_68949 | chr17:1480336-1481912 | H9 |
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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 |
GH17I001573 | chr17 | 1477152 | 1482396 |
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Enhancer Sequence | ACCACATCTG GCTAATTTTT TGTATTTTTA GTAGAGACGG GGTTTCACTA CGTTGGCCAG 60 GCTGGTCTCA AACTCCTGAC CTTGTGATCT GCCTGCCTCG GCCTCCCAAA GTTCTGGGAT 120 TACAGGCGTG AGCCACCGCG CCCGGCCCTG CTGGGTGGTT CTGCAAAGTG TTTCTCTTTG 180 GACCAGCTCC AGGCCCCAGA CTCTGGGGAG GGCCCACCCC ACTCAGCTGT GCCCAGGGCC 240 TGTGGGTGTC TGGCTGAGCC GAGTGGAAAG CGTGGTGCCA GCGGGGACCT GCGGTTTGGG 300 AAACAGGCCC AGAGAGGAGT GTGGAGGCTG GGCTTGGCTC TGCAGTGCCC TCGTCCAGAG 360 AAGCATTGAG TAATCGCGGA AACTCAGCAC CACAGATCCC GCCCCCCTCC CTCAGACCCT 420 GCCAGGACAG CCACAGCTTC CTCCAGGCCT GGGGAGGGGC AGGCGGAGGG CAAGCGGAGC 480 TGGGATTACC CCAGGGGCTG TTGCGGGAAT TGGGAGAGAG TTCCGGGCTA AATCTTAGCA 540 CATGTCAGGC TCTGCTGGCC CAGAGGTGGG AAAGGAATCC CAGCAACACA TGAGCTGGTC 600 CCACATCAGA GACTGTGGAT GATGATGTTT GAGTTTCAGT TTTTGGGTCA AGGCCTGAGC 660 CAGAGAAGAA GGAACCACTG TGGTTCCTTT TATGTTTCTG GGGCTTCTTG GAAAAAGATA 720 CAGGTTTCAT TTTAGCCAGG GCTGGAGAAA GCTATGGCCA GAGCTGGGCG CACTGAGGCT 780 CTGGATGGGC CCGTCTGGTG TATTCTGGAC TCAGTCACCC ATGTTGCTGC CCGTGATGAG 840 GGCAACTGGA ACTTCCGCAT TTAGCTTCAG GCAGCCAGAA CCTACCCATC CTTCCCAGTG 900 AGCAGCCAGG GCCAGCCCCA GGACTCGGCT GTAGTGGCCC CTGAGGCCAT AATGAGCTGC 960 ACAGGTGCCT GACCCTGGCT GGGGGAACTG ACTTCGTGTT GAATGCCAAG GCTTGTGAGC 1020 ACCCAACTGT CTGCCCACTG ACCTGCTTCC CACGAGGTAT GGCCTTTCCC TGAAACACCC 1080 AGCAGAAACC CTGGTACCTG TCCCCTGAAG CAGGAAGATG AGCCCTTCTG GGACAGGCTG 1140 ACCCTGCCTC AGAGTCTCAG TCCCACCAGC AACCTCCCCC CGGCCATTCC CACACCCTCG 1200 CCCACCAGGC CACCTGCGGC TTCCAGGACT 1230
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