Tag | Content |
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EnhancerAtlas ID | HS091-36129 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:1730520-1732020 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr4:1731764-1731776 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr4:1731768-1731780 | GTTTGTTTGTTT | + | 6.32 | MIXL1 | MA0662.1 | chr4:1731547-1731557 | TCTAATTAAC | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34415 | chr4:1726014-1731280 | HCT-116 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 1731500 | 1731747 | chr4 | 1731421 | 1731488 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I001725 | chr4 | 1726945 | 1730790 |
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Enhancer Sequence | GTGAGGATGG GATGGGGAGC GTGGCGTGGG GCAGCTGCCC TGCAGTGTAT GTGGTCCAGG 60 ACCCGAGGCC AGAAGTGTCA TCAGATACTC CTTTGAGGCC GGGTAGGTTC TGCCTGAGGA 120 GGGGCCTCTG GATAAAAACA GGGCTCAGGT GGCTCCCAGC TGAGGGTGCT TGGCCTTGCC 180 TTGGCTGCCA TGCATCTCTT TAGTGCTCCT GGCCTAAGGA GGGATCCAAT AAGGGCGGGC 240 TCAGGCCAGA AGCCAAATGC AACCAACCCT GGGCAGGACC CTGTCCCCCA GTCATGTTCC 300 TCCTCAGGTG AACTTGACTT GGGTGTGTAA CTCCAAAAGC CAGGCAAAGC CTGTTACTGC 360 CTGGGTGGCG TCCGCTGCTT GCTGGGGTCT TGGCCGTGGG TCTGCTGCCT CCTGGCTGAA 420 TGGTCTTAGG CTACATCTCC TAGAGTTGCT CAGTGGGAGA TTGTCCTGCC TGTAGGGTCC 480 AGCCCTACTG GGTCTGTGGG TTTTTTCTCC TCGTGTGCAT AGACAAGAGA TTGTACAAAT 540 AAAGACACAA GAAAAAGACA GAAGAAAAGA CAGCTGGGCC CGGGGGACCA CTACCACCAA 600 GGCACGGAGA TCGGTAATGG CCCCGAATGT CTGGCTGCGC TGTTACTTAT TGGATACAAG 660 GCAAGGGGAC AGGTTAAGGA GTGTGAGCCA TCTCCAATGA TAGGTCAGGT CACGCAAGTC 720 ACGTGTCCAC TGGGCCCTTC CCTGTTTGGC AGCCAAGGCG GAGAGAGAGG ACAGCTGACG 780 CCATTATTTT TTCTATGTAT TTCAAAGACT TTAGCACTTT GACTAATTCT GCTACTGCTA 840 TCTAGAAGAC AGAGCCAGGT GTACAGAGCG GATCATGAAA GTGGACCAGG AGCGTGACTG 900 CTGAAGCACA GCATCACAGG GACACAGGCC TCTGGATGGC TGCGGGCGGG CCTGACTGAT 960 TCCACAAGAG ATGGTGGAGC AGAGTCTTCT CTAACTCCCC CAGGGAAAGG GAGACTCCCT 1020 TTCCCAGTCT AATTAACGGG TGCCTTCCCA GGCACTGGTG CTACCGCTAG ACCAAGCTAG 1080 GTAACGGGTG CCTTCCCAAG TGCTGGTGTT ACCGCTAGAC CAGGGAGCCC TCCAGTGGCC 1140 CTGTCCGGGC GTGACAGAGG GCTCACACAC CTCTTCCGGT CACTTTCTCA CCGTGTGCCT 1200 TCACCTCCTA TCTCTATATG GCCTGGTTTT TCCTAGGGTT ATTTGTTTGT TTGTTTGTTT 1260 TTTGAGACAG AGTCTCGCTC TGTCACCCAG GCTGGAGCGC AGTGGCGTGA TCTCGCCTCA 1320 CTGCGAGTTC TGCCTCCCGG GTTCACACCA TTCTCCTGCC TCAGCCTCCC GAGTAGCTGG 1380 GACTGCAGGC ACCCGCCACC ATGCCCGGCT AATTTTTTTG TATTTTTTAG TAGAGACGGG 1440 GTTTCACCGT GTTAGCCAGG ATGGTCTAGA TATGACCTCG TGATCCGACC GCCTCGGCCT 1500
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