Tag | Content |
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EnhancerAtlas ID | HS048-33232 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr7:1452080-1453020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr7:1452599-1452618 | CAGCGCCACCTGCCGGCTA | - | 6.78 | KLF13 | MA0657.1 | chr7:1452738-1452756 | AGGCCACGCCCCTTGTAG | + | 7.34 | KLF14 | MA0740.1 | chr7:1452739-1452753 | GGCCACGCCCCTTG | + | 6.08 | KLF5 | MA0599.1 | chr7:1452682-1452692 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr7:1452679-1452694 | GAGGCCCCGCCCCTA | + | 6.06 | SP1 | MA0079.4 | chr7:1452660-1452675 | GAGGCCCCGCCCACA | + | 6.45 | SP1 | MA0079.4 | chr7:1452737-1452752 | CAGGCCACGCCCCTT | + | 6.7 | SP3 | MA0746.2 | chr7:1452739-1452752 | GGCCACGCCCCTT | + | 6.02 | SP4 | MA0685.1 | chr7:1452660-1452677 | GAGGCCCCGCCCACAGC | + | 6.13 | SP4 | MA0685.1 | chr7:1452737-1452754 | CAGGCCACGCCCCTTGT | + | 6.76 |
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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 |
GH07I001411 | chr7 | 1451488 | 1453169 |
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Enhancer Sequence | CCTGGTGCCC TCCCAGCTCA AGGCCTTGCC TGACTACAGA TGCTGTCCCT GCCTCGGGCC 60 TGCCTGGCTG ACAGCGGGCA TCTGGGCCAG CGCTGCAATG CTGCCAGGTA GAAGTGCTCC 120 CTCCAGGCTG GGGGGACCTG CAACTCCCGC CCGGGAGTCC CTCAGACTTG GAGTGCTCTG 180 AAGAAAGCAA GCCAGCGGCC AAGTGGGCTA TGGGCCAGGT GCGGGAAGGC TCCAGACCCG 240 GGGCTGCAGG GTTGGAGAAG GGCGCAGCAA AGGCCTGGAG ACAGCCTGAA CCAGGGATTC 300 AGGATGGAAT GGGTCTGGGT CAGGGAGCCA GGGTGACCGT GGGCCGCACA GGCCTGCGCG 360 CGCGGGTGCA CGTGCGTAAT GGATGCACAC GCATGCAGCT GGTGTGCGTG CAGTCGGGCG 420 CACCTGTAAC CGGTGCGCAC CCCGCGTCTG GCGTGCAAGT GGGAGCACCT GGCCCAGCGC 480 CCAGCGGGGC CTCGCCCGCC GCTTTCTTAG GAAACGCCGC AGCGCCACCT GCCGGCTACG 540 CGGTCTCAGC TGGACGCGGG CGGGGAGGGC GCCGGGCCAC GAGGCCCCGC CCACAGCCGG 600 AGGCCCCGCC CCTAAAGACT ATCTTGGTGC CCCGCCTCTT CAGACTCCGC CCGATTCCAG 660 GCCACGCCCC TTGTAGGCGT GACCGAGGAC GCTGGTACCC GGACCTGGAC TTCGCAGGGT 720 CTTGGAGGGG CGGGCAGTGG GGGATCTCCG CTTTGGGTCT CCTGGCTGCA AAGCGAGGAC 780 AACTATGAGC CTTAAACGCA CACCAGGAGT GTAATAAGAG CATCTGCTGC GTCACTAACT 840 CTTCCCATTT ACCGATGAGG AAACCAAGAC AGAGAAGTCA AGTCACCTGC CCAGAGTCAC 900 GCAGGAGAAA GTCGTAGGCC GGCTTTGAGC CCAGCATCCT 940
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