Tag | Content |
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EnhancerAtlas ID | HS176-41042 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr8:145597800-145599130 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr8:145598581-145598592 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr8:145598582-145598592 | GGGGCGGGGC | - | 6.02 | MEF2A | MA0052.3 | chr8:145598719-145598731 | GCTATAAATAGC | + | 6.32 | MEF2B | MA0660.1 | chr8:145598719-145598731 | GCTATAAATAGC | + | 7.22 | SP2 | MA0516.2 | chr8:145598579-145598596 | GGGGGGGCGGGGCAGAG | - | 6.19 | SP3 | MA0746.2 | chr8:145598580-145598593 | GGGGGGCGGGGCA | - | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGACTCTCCC GGCCCGGGGC GCCCGAGATC CTGCACACCA GCCCCAGAGA CCCGAGACCC 60 GCAAGTCCCC AGACCCCGCC CTAGAGACCC TCGGGGCTTT TTCCCTCTTT TTTTTTGAGG 120 CAGGGTCTCG CTCTGTCGCC CTGGAGCGCA GTGGTGCGAT CTCCGCTCAC CGCAGCTTCC 180 GCCTCCCGGA CTCAGGCGAT CCTCCCGCCT CGGCCCCGCA AGTAGCTGAC ACCGCAGGCG 240 TGACCGCTCC CGGCCGACTC TGTTTAGCAG AGTCGGGGTC TCGCCGTGTT GCTCAGGCTG 300 GTCTCGAATT CCTGGGCTCT AGCGATCCGC CCGCCTCAGC CTCCCCGAGA GCTGGGATTT 360 CAGGCGGGAG CCGCGCCCGC AGCCCTGACG CCGCCTGCAC CGGGAGCCGC AGGGGCCCCT 420 CCGCCCAGCC CGGAGGCGGG TGCCCGGCGC CCCGGAGAGC GCGATCTCCA GAGGGCAGGG 480 GCCCCGCGGG GAAGCCTCAG GCGCCGTTCC CCTCGCGAGG CGGCCTCCCG GAATCACGGA 540 CGCCTCCCTG CCCAGCCTGC TGCCCCGGAC CTCCTTCGCT CGCCTCCCCG CCGGGCCTGC 600 CCTGCCCTGA GGCGGCGGGC GGGCGGGGGC TGCAGGCCGG GCTCTGCTCT GAGCGCCCCT 660 GCGTCGTCTC AGGGGCGCGC CCCCCATGGC TCCGAGGCCC CCTCTCTCAG GCTCTCGGCG 720 TCTCCCCGCT CCCACGTCGC CGCCGGGTCC CGTTGCTCTG TCCCTGCGGT TAGGACTGCG 780 GGGGGGCGGG GCAGAGGCCT TGACACGCAT CTTACCCACC CCCTTCCAGA AGAGATGAAG 840 GGGCTCCCAG CGCCGTTCCT TTTTTTCTTG GAATGTCAGC AGAGCTTGTG TTTGGCGATA 900 AGCTAGCCTT GCCCGTCTGG CTATAAATAG CACAGATGGA CGGCCCACTC GTGCCCCAGC 960 CCAGCTGTGT GACCCCAGGG TGCTTCATGG GCCGGGGAGG TGGCCTTCAG TGCAGCTCCT 1020 TCCAGGTGAC AAAGTCTTCC CACGTGCAGG CCACTCAGTC CCTCCCCAGC CCCAGCGAGT 1080 GGACAGGTCG GTTTAGCCTC TGGTTAGGAG CTGCTCATGG CCAGTGAGCA GGGCTGGGTC 1140 CAGGCGGCGT TTGAGGGCTG GCTGGGGCTG ACAGGGTCAC ACACCCTGGG AGAAGGACAG 1200 TGTCTGTGGT CGCCAGACCC ACTTACCCTG CCCAGACTCC CAATCTGTCT CTTCCTAACT 1260 TTGGGGACAA TTATGTGCCT CAGTTTCCCC TCATGTTGAG GTGCACAGTG CTGTTGGGTT 1320 CCCCAGGCTC 1330
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