Tag | Content |
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EnhancerAtlas ID | HS048-38211 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr9:132359670-132360990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr9:132360121-132360134 | TTCGGGAACATTC | + | 6 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_32072 | chr9:132358214-132361177 | Gastric | SE_34237 | chr9:132356536-132361476 | HCT-116 | SE_35734 | chr9:132358097-132361117 | HepG2 | SE_54057 | chr9:132358174-132360891 | Spleen | SE_56758 | chr9:132358957-132360994 | VACO_400 |
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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 |
GH09I129594 | chr9 | 132357267 | 132361100 |
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Enhancer Sequence | CCCGGCCCTG TCCCGGGAAG GCTGGACCGG CCCGCGGCTT GCCCTTTCAA GTCGGCCTCC 60 CGGAGTCTCC GGAGCCGTCC GAGCGCTGGG GCCGCTGGCG CGGACTTCAA AGCCCGCCGC 120 CCCCAGCCAG ATCCGGTTGC GGGTGGGGCG GGCGAGCTGG GAGGGAGGCG GGTTTCGGTG 180 GATTCCCCTT TCATCCCGCG GCTGCAGCCG GGCGCAGACC TCGGGGAGGC CCGGCGCGTC 240 CCCGCTGGGC AAGTCCCTGC AGGGCAGCGA CCGGGAACGG AGGGCTGGGG ACGCCACGAG 300 GCCGCGCCGC AGGGCGGGGG AGGCCTGAAC CCAGACTGGG GGCTTCGGAC CCGCCTGCGC 360 TGTGGGACCT CAGGCCAGCG CCTACCTGTC GCTGGGCCTC AGCTTTCCTG AATGCCCTAC 420 TCCCTGCCCA GGACTCCTCT GGGGAGGGGC ATTCGGGAAC ATTCAGTGGC CCTTGGACAG 480 CTGAGATAGG AACAGGAAGC TAAGCTGGGA GCCCGGGCTC TCCTTGGGGT ACCTGCCCGA 540 CCCCACCCAT CCCACCGGAG AGGAACCGCT TCCTGCATCA GCCAAGCCCT GCCCGCAGTG 600 TAACCCGTGG TCCAGCCTGG CCCTCTCTGG GCCTCAGCTT CCTGGAAGGC TGAGGGGGTG 660 GCGGCTGAAT GCCCTCCCTC CGGGTTGAGG TGTAGCGCAT TCCTTCTTGC CGTCCTGTTT 720 CCCGGTCCCT AAAGTAAGGG TGGAGGGAAA TGGCTCTCCC TTTCTGGTGT AACCATAAGG 780 AAGTGGCTGC CTGACATTCT GTAGCCGTCC GCGTGCCCCA TCCAAGCCCC ACAGAGCCCT 840 GTGTGTAGAT TAAGAACATC CTTTTTTTAG GTGAACAGCC TGAGGCAGAG GGGGTGTCGC 900 TTGCCCCAGG TCTCAGCTGG CAGGAAAACT GGGACTTGAC ACAAAGTTAC TTGGGCTTTC 960 CTCCACCTTC CTCCCTGCCC GTGGTCCCCA CTGATTGCAA AACAGTCATA GGGGAGGTGA 1020 GTCCAGGCTG GGAATTTGGA AAGCAGACAC TGACATAACG TGGGGTGCAG GCGCAGGAGT 1080 AGTATCACCC CCGCTTTACA GACCCAGAAA CGGACACCGA GAGGTTGCGA AGCCAGACAA 1140 GGGGCAGAGC TGGGTATTGA CGCAGATTTT TGGGGCCCCA GAGACTTGAG GTTTAGCCAC 1200 TGCCTCTGGG GTGAGAGGGG CAGGGCACTT ACTGTGTGTC AGGCCCAGGC TGGGAAGCAT 1260 CTTGATCAAC ACAAGAACCC CAGCTGGGAG GTGGTGGTGT AGGAAAGGGG TCCAGATCCA 1320
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