Tag | Content |
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EnhancerAtlas ID | HS052-37462 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr8:116439190-116440380 |
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) |
FOSL2 | MA0478.1 | chr8:116439975-116439986 | ATGAGTCATCC | - | 6.62 | JUN(var.2) | MA0489.1 | chr8:116439975-116439989 | ATGAGTCATCCTTC | - | 6.35 | JUN(var.2) | MA0489.1 | chr8:116439970-116439984 | AAGAAATGAGTCAT | + | 7.12 | JUNB | MA0490.1 | chr8:116439975-116439986 | ATGAGTCATCC | - | 6.62 | Lhx3 | MA0135.1 | chr8:116439521-116439534 | AAATTAATTAAAT | + | 6.07 | TFAP4 | MA0691.1 | chr8:116439931-116439941 | AACAGCTGAT | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_55889 | chr8:116437383-116449753 | u87 | SE_67761 | chr8:116437383-116449753 | u87 |
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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 |
GH08I115426 | chr8 | 116439135 | 116443622 |
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Enhancer Sequence | CAGGATCATA TTCTAAAAAG CATTTTTGGC CAGGCGTGGT AGCTCATGCC TGTAATCCCA 60 GTGCTTTGGG AGGTCAAGGT GGGAGGATTG CTTGAGGCTA GGAGCTTGAG ATCAACCAAG 120 GCAAACACAG CAAGAACGTG TCTCTACAAA AAGTTAAAAA AAAAATTAGT TGGGTGTGGT 180 GGTATGCATC TATAATCTGA GCTACTCTGG AGGCTGAGGA GAGAGGATGG TTTGAGCCCA 240 GGGGTTCTAG ACTGTAGTGA GCTATAATCA TGTCACTGTA CTCCAGCCTG GGCAACAGAG 300 CGAGACACTG TCTCTAAAAT AGATAAATAG AAAATTAATT AAATAAAAAA GAATTTTTGA 360 ATCAACTATT TAATAGAATA CTCTTGTTTG ACTATCTTTG TCCCTTTTTA AATAATCATC 420 ATTGCACATA TGTTTGCAGG ATAACATATG ATAGGCCTAG TCTCATTATC TGATATCCTC 480 AGAATGATCC TAAGAGGCAA GTATTATTAT CATTATTATT ATTATTCCCT CCACTTTATA 540 GATGAGAAAA CTGAGGCTTA GAAGCAATTT GCAACTGCTG AATAGTAGGG CTAAGATATA 600 AACCCAGGTT GCCCTCACTT CAAAGCCACA GTGAACCATG TTTCAGGCCT TATTACTAAA 660 GAGGAGATTG GGGAATTTTT ACCAAAAATA TTACACCATA TCCTGGCCTT AAAGAACGCT 720 TATCTCTTCA AACCACCCAA TAACAGCTGA TTGAAATTAT GCAAGTTTTG AGGTACCAGA 780 AAGAAATGAG TCATCCTTCA TCAGATATGG CAACGAGCTG TTTTGAGGTC GACAGACACA 840 GTCATAGCCA GAGGAACAGA GCACTTGGCT GATGGAGGGG GCAGTGCTGG GGAGGGGGGA 900 GGGGTGCAGT ACATGTGTTT TGATCCTGCT GTGTCAAAAA AAATAAAAAA AGTATGTGAA 960 ACAGGCCGCT GCTTAAAAGC AGAAGTTGGT GACACCACTG ACTTAGCCTC TCATAGCGCC 1020 TGCTACATGG GAGGTTAGCT GTGAATGAAA GTCTCTCTTT GCTTTTGCAG AAGACTTGGC 1080 TAGAGTTGGG GCAAGAAAAA TGGTGCTGGG GTTTTGACAT GCTCTGTAAA CACACATGTT 1140 CAGGTAACAA TTTACTAGAT TTCTTTTATA TATGTGTATG TTCCAAGGCA 1190
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