Tag | Content |
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EnhancerAtlas ID | HS091-36135 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:1803750-1804640 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr4:1804361-1804382 | GGCCCTGTCCAGGGTGCAGGT | - | 6.86 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_25282 | chr4:1794206-1804359 | Colon_Crypt_3 |
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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 | AGGTGGGCCA CCGTGTGCAC GTGGGTGCCG CCGCTGGGGC TCCTGGGCTG GCCCCAAGGG 60 TGCCCCTTGG CTGCGGGTTG CGTGAGGATT TGGGTCTAGG GGTTGGAGCT TCGGGGGCAG 120 AAGCTGTGGG GGTGCTTGTG GGGCCAAGTC TCAGCCACCC CACACCTCAG GGCCATAGGC 180 AGCTGCGTTG GGACCCGTTT CCGTGTCTGC AGAGGGCCAG CCTCAGCCAC TGAAGTCCCT 240 GACATGGAGC TGCCCACGGG CTTCTTGGGG GTGGGTGCGG CTTGGGCAGC AGTGGTGCCC 300 CAGGACAGGA GGGCAGTGTG GCCAAGCCCT CCAGGCCCCC TCTGGGCCTC AGAGGCGGTG 360 GCTGAGCCCC GACCTGGCCG ATTGGCTCTC GTCAGCTGTG TGCAGTGGGG CCCGAGCTCA 420 CTGTCTGCCC GCCTCCTGAA GCCCTTAGCT TTGTTCCCAT GGCTGCCGGG TGGGGGCCAC 480 TGAATTGGGA CGGTTGCGAC ACTCAAAGCC CAAAGAGAAA CATCTGTTCA GAGAGAAGAC 540 GGTCTCTTGG GGGCGGGGAG CAGGCGCAGG GCGAGGGTGG AGTCCAGACC CCGCCCAGAG 600 AGGCCGCCTC GGGCCCTGTC CAGGGTGCAG GTTCTGCAAG AGCCCGGGGG AGGGCAGGCC 660 AGTGACCAGA GGTTGTCTGA GGGTCTGGGC TGGGTTGTTG GGGTGGAGGC AGAGACGTGC 720 ATCCTGTGAA ACCACAGCCA CCGTGAAGTG CCTCCACGCC TCCTCCAGGC AGCCTTTGGG 780 GCTGACGCAG CCCAGCCTCG ATCTGTACCT TGGGGGTCTC CCACATCCTG CCTCGTGCCC 840 GGCGGGGCTG CCTCGGGGGC GTGCCTGAGC CGGGTCTCTT GTCCCCGCAG 890
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