Tag | Content |
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EnhancerAtlas ID | HS091-18251 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:84095850-84096900 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr16:84096525-84096544 | GGGCGCCCCCTCGTGGCAG | - | 6.89 | Nr2f6(var.2) | MA0728.1 | chr16:84095944-84095959 | TGAACTCCTGACCTT | - | 6.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33714 | chr16:84095967-84097739 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I084062 | chr16 | 84096381 | 84096630 |
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Enhancer Sequence | AAGCAGCTGG GACTACAGGC ACACGCCACC ACGCCTGGCT AATTTTTGTA TTTTTAGTAG 60 AGACGCGGTT TCACTGTGTT GGCCAGGCTG GTCATGAACT CCTGACCTTG TGACCCACTC 120 ACCTCGGCCT ACCAAAGTGC TGGGATCACA GGCGTGAGCC ACCGCGCCCG GCCCATTTTT 180 GATTTTTAAA AAGACCCATC CCAGTCTAGG GATTTACATA AATGCCAGGA ATGTAGTCAA 240 CTTCAGCCTG AAACGGAGGG GCACACACAC ACCTCTCAGC GCACGCTGTT AGTGCCTCAT 300 TCTTGTCACT CACCACCCGC CCTGTGCCTC GAGTTCCCCA GTGGTCACAG CGCATTAGAA 360 GGTTGCCTTT CAGTCCTGGT GTCATTATCA TCTCACCAGG TAAAAACATG GAGCACTTTT 420 ACCATTCTTT CTCCCCTTTA CAAAATGAGA AAAATAGTCT GTGCCCAACC TCAAGCCCCC 480 AAATCCAACG GATGCATCGA GAGACTGACA TAAAGACGCG GAGGGAAGAG GACTGGCATG 540 CCTATTTGCC TCCCCTTCAC GCCTCGAGAT AACAAACGCT CTTCACTGAT AAAGGCTAAG 600 AAAAGCCCGA ATTCCAGGTC TGGAAGGACA GCCAAGAGCC AGCCCTCCAG TAAAAGAGTG 660 AGTCAGACCA GAGAAGGGCG CCCCCTCGTG GCAGTGCCCA CAAAGTCCAG GCAGCACGGC 720 GTAGGAAGCC TGGGAGGGGC AGGCCCCAAG GAAGTCAGGG AAGGGACTCT CCACCACAAC 780 GCGGGAGTCC CGCCTCCGCT GGCCTCAGGA AGGTGAAGAT GGAGAAGAGG CATCATGGCC 840 CCAACAAGTA GCTTTGTTTT GCTTATTAAA TGTGTGCACA CTCAGACACC TATCAAAATA 900 TTCCAAGCAA TCAAAGTGAC TGCAACATCT CCAGCTGAGC CTGGCTCAAG TGAACAGATG 960 TCGGCTGATC TGCCAGCATC TCACGGGCGC CTTTCCAGAG ACAAAGGGAA GAAAGGATCT 1020 GAGTGCCGAA GTCACAAAGT CCATCTGCGT 1050
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