Tag | Content |
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EnhancerAtlas ID | HS136-19370 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr8:94944350-94945610 |
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 | Foxd3 | MA0041.1 | chr8:94944449-94944461 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr8:94944453-94944465 | AAACAAACAAAC | - | 6.32 | 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: 2 | Chromosome | Start | End |
chr8 | 94944837 | 94944971 | chr8 | 94944432 | 94945524 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I093931 | chr8 | 94944033 | 94949536 |
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Enhancer Sequence | GAGGCAGGAG AATCGCTTAA ACCCAGGAGG CAGAGGTTGC AGTGAGCCAA GATTGTGCCA 60 TTGCACTCCA ACCTGGGTGA CAGAGCAAGA CTGTGTCTCA AACAAACAAA CAAACAACAA 120 TTAAAAAAAA GAAGAGAATT GAGGGATGAC TTTCTTGGAA GAAGGCAGAA CTCGTGTTTG 180 AAGAGCTCTG AGTGCCTTTC ATATGGGTAG AACATGCACT GGTGGGGAGC TGTGGTGGGT 240 GATGAGGTGG AAAGGTAGAA ACAGCACAGA AGAGCCCTAA GCAAATACAC AGTCACTCTG 300 GAGCACTTTT GCAGCCAGCA AAACTTTAGA GACAGAACTG CTTGAGAAGG CAGAGGTCAA 360 CCAAGACAAG CATGGGATGC AAGAGTTGGT GGAGGCAGGC GTGGGAGGAA GAAGGACAAA 420 GGAAGGTCAG CTGGACCCGT GCCAGGCTGA GATCTGGCTT CTAGCCACTC ACAGATAGGA 480 GCCTAGACGG ATTTAAGTGA GGAAGTGTTG ATGGTTAAAC AAGAGAACAT CCGTGTGATT 540 TGCATATTGC CATTAGTCAT TCGTGGGTCT GCAGTCAAAT TTAGTAACCT GGTGTTTAAT 600 TCAAACATAG GCATATTTTT GTTCCCCTCA GTTCCTTGGC TACTATAGTA CACTTACTGA 660 ACACTACTCA GGTATTGGGC AACTTAAAAG CCACTGAACC TGAGTAACCT ACCAGCCATC 720 CATCAAAGTC TTGGACCATG ATAGCTGGAT TGAATTACCA GCCACAGGCT GGTTCAGTCC 780 AATCTAGCAA GTGTGTATTG GGTTCCTTCA TTGTTTTAGG TACTAGGGAT ACGTGGTAAT 840 CAGCCTTCAG GATGGCTCTC AGTGACCCCT GCCTCCTGGT ATTTACATCC TGCGTAGTCA 900 ATACACTCCT AGGATTGGGT TAGAGTATAG CAGATGAAAT GGGATGGCCC TCCTGATATT 960 AGATTGTAAA AAGACACTGC AGCTTCTGTC TTGGACACTG CTTTGCTCTT GGATAACTGA 1020 CTCTAGGAAG AGCCATGCTG TGCGCAGCCT TCTAGAGAGG CCCATGGAGA AAGGGACTGA 1080 ATCCTTCTTC CAACAATCAC ATGAGTGAAC TTGGAAGCAG ATTTTGCAGT CCCAGTGACG 1140 TCTTCATGGC TGCACCCTTA GTCAACAGCA TGACTGTGAC CTCATGAATG ACCTTGAGCT 1200 AGAAAAGCTG CTATCAGGTT CTAAACCCTC AGAAACTGCG TGAGAAATAA CTTTGTTGTT 1260
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