Tag | Content |
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EnhancerAtlas ID | HS053-21724 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr2:109830010-109831410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr2:109830433-109830444 | TGTGGATTGGG | - | 6.14 | Gata4 | MA0482.1 | chr2:109830698-109830709 | AAGAGATAAGA | - | 6.02 | Spz1 | MA0111.1 | chr2:109830287-109830298 | AGGGTTACAGC | + | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_43595 | chr2:109828645-109837604 | MM1S | SE_67371 | chr2:109828645-109837604 | MM1S |
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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 |
GH02I109212 | chr2 | 109829393 | 109831464 |
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Enhancer Sequence | GCTCTTAAAG CAAGGAAGAT GGGGGCATTG GGTGGACACC AGCTGTGTCC AACACAGCAG 60 GCACCTTTGA GCCATGTCAG GGCAGCAAAC TGTGTGTCTA CACAGGCATA CTAAGGTCAG 120 GTCAAGATGG CTTCATCTGT CACGTGTCAG AGCCTGGCCT TTATCCTTTA CCTTGAGTGG 180 GGAACGTGGG GATGGTTTTA AATAGGAACG TGACGTGGTC TCACTGTGGT GTGGTGTGAT 240 AGGGTGTGGT GTGGTGTGGT GGATGGGCTG GAAGGGCAGG GTTACAGCCC GTGGGTCGTT 300 CTGAGGTCAC TGAAGTAACC CAAGCCCATG AGGCAAAGCC TCCCGGGACA CTGGTGTCAG 360 AGTGTGGAGG AAGCTGACTC AGTGACTGCC CTCAGAGGCC TGGAGCAGTC CCTGCAAAAG 420 ACCTGTGGAT TGGGTGGACG TGGCGGGCAG GGGAGGGAGG AGCTCTGAGA CCAGCCCTGC 480 AGTTCTGGTT GGAGGAAATG GAGGGCAGGC AGTGGTCACT GGACGGCGAG GAGGAAGGGG 540 TGTTTCTGCC AATTGTCTTG GGTGTGCCGG GTGCCCCCAT GCTGCGTCTA GGTAGGGGCC 600 TCAGCAGGCT GTTGGAGGTG AGGCTAAGAC GCAGACTGGA AGTGACTGGA AATAAAGCTG 660 TCAGCATGTG GTTTATGGGT AAAACCACAA GAGATAAGAT CACCCAAAGG GAGTGGCCCC 720 AAAAGCTGGG GCAGAAGGGC TTGCCTTATT CTCCTGGGAG CATTGCTACC CTGGCAGAGG 780 AGGGGCCTTG GGGCTGTGGG GGCAGCAGGA GGCCGGGGCC ACGTGTGCTG TGTAGAGAGT 840 TCTTGTGTAA CAAACCTGCA CACTGTGTAC ATGTACCCTA GAACTTAAAG TATTAAAAAA 900 AAAGAGTCAT AGAAAAGAGA AAAAAAAAAA AAGGAGTGGA GCCCAAGCCA GCCAGGCCCT 960 GGCGTAGAAG ACCTGTGAGA CAAGGACTAA GAAATTTCAT TGACATGAAA CAAAAGGGGG 1020 ATGATTGAAA GACAGCCAAA CAGGAATCCT TTTTGAGGAG GACATCTGAA CAGCCCTGGA 1080 AGAACGTCTC TGCCTGACAC TCTTGCTGGC ATCTGTGGGC TCTCTCTGTC CCGTGGACAG 1140 GACAATCAGA AGATGGGCTC CACTCCAGCT GCAACTCTGG TGACATTTAG CTGTGTGGCC 1200 TTGAGCCTGT GGCTTCACCC CTCTGGACTT GCGTCCTCAC CCCTAAAGGG GAGCAAGATC 1260 TATGTATATT GGAGACTGAG TTCCAAGGGC TGCTGGGGGT GACGCGGACA GCAGTGTTTT 1320 GGGAGATCTG AGACTTGGAG GGTGGTAGGC ACTGACACCA CAGCCCAGGA GCTCTGCACC 1380 AGCTGTAGTG AGCTGAGGAG 1400
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