Tag | Content |
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EnhancerAtlas ID | HS034-29428 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr8:94944460-94945640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr8:94945536-94945547 | AATGACCTTGA | - | 6.32 | Esrra | MA0592.2 | chr8:94945537-94945548 | ATGACCTTGAG | - | 6.02 | Esrrg | MA0643.1 | chr8:94945537-94945547 | ATGACCTTGA | - | 6.02 | POU2F2 | MA0507.1 | chr8:94944884-94944897 | GTGATTTGCATAT | + | 6.04 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_33930 | chr8:94942359-94946105 | HCC1954 | SE_34232 | chr8:94942255-94952002 | HCT-116 | SE_41045 | chr8:94942335-94946404 | Left_Ventricle |
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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 |
GH08I093931 | chr8 | 94944033 | 94949536 |
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Enhancer Sequence | CAAACAACAA TTAAAAAAAA GAAGAGAATT GAGGGATGAC TTTCTTGGAA GAAGGCAGAA 60 CTCGTGTTTG AAGAGCTCTG AGTGCCTTTC ATATGGGTAG AACATGCACT GGTGGGGAGC 120 TGTGGTGGGT GATGAGGTGG AAAGGTAGAA ACAGCACAGA AGAGCCCTAA GCAAATACAC 180 AGTCACTCTG GAGCACTTTT GCAGCCAGCA AAACTTTAGA GACAGAACTG CTTGAGAAGG 240 CAGAGGTCAA CCAAGACAAG CATGGGATGC AAGAGTTGGT GGAGGCAGGC GTGGGAGGAA 300 GAAGGACAAA GGAAGGTCAG CTGGACCCGT GCCAGGCTGA GATCTGGCTT CTAGCCACTC 360 ACAGATAGGA GCCTAGACGG ATTTAAGTGA GGAAGTGTTG ATGGTTAAAC AAGAGAACAT 420 CCGTGTGATT TGCATATTGC CATTAGTCAT TCGTGGGTCT GCAGTCAAAT TTAGTAACCT 480 GGTGTTTAAT TCAAACATAG GCATATTTTT GTTCCCCTCA GTTCCTTGGC TACTATAGTA 540 CACTTACTGA ACACTACTCA GGTATTGGGC AACTTAAAAG CCACTGAACC TGAGTAACCT 600 ACCAGCCATC CATCAAAGTC TTGGACCATG ATAGCTGGAT TGAATTACCA GCCACAGGCT 660 GGTTCAGTCC AATCTAGCAA GTGTGTATTG GGTTCCTTCA TTGTTTTAGG TACTAGGGAT 720 ACGTGGTAAT CAGCCTTCAG GATGGCTCTC AGTGACCCCT GCCTCCTGGT ATTTACATCC 780 TGCGTAGTCA ATACACTCCT AGGATTGGGT TAGAGTATAG CAGATGAAAT GGGATGGCCC 840 TCCTGATATT AGATTGTAAA AAGACACTGC AGCTTCTGTC TTGGACACTG CTTTGCTCTT 900 GGATAACTGA CTCTAGGAAG AGCCATGCTG TGCGCAGCCT TCTAGAGAGG CCCATGGAGA 960 AAGGGACTGA ATCCTTCTTC CAACAATCAC ATGAGTGAAC TTGGAAGCAG ATTTTGCAGT 1020 CCCAGTGACG TCTTCATGGC TGCACCCTTA GTCAACAGCA TGACTGTGAC CTCATGAATG 1080 ACCTTGAGCT AGAAAAGCTG CTATCAGGTT CTAAACCCTC AGAAACTGCG TGAGAAATAA 1140 CTTTGTTGTT TTAGATGCTA AGATTTGAGT TAATTTGTTA 1180
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