Tag | Content |
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EnhancerAtlas ID | HS168-02426 |
Organism | Homo sapiens |
Tissue/cell | RPE |
Coordinate | chr22:39541770-39542490 |
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) |
KLF5 | MA0599.1 | chr22:39541797-39541807 | GCCCCGCCCC | + | 6.02 | USF1 | MA0093.2 | chr22:39541781-39541792 | GCCACGTGACC | + | 6.62 | USF2 | MA0526.2 | chr22:39541779-39541795 | CGGCCACGTGACCTCC | - | 7.66 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_06470 | chr22:39539496-39550242 | Brain_Hippocampus_Middle | SE_32434 | chr22:39539806-39549575 | Gastric | SE_54097 | chr22:39539642-39549819 | Spleen | SE_63135 | chr22:39510695-39550154 | Tonsil |
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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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Enhancer Sequence | AGATAAACAC GGCCACGTGA CCTCCCCGCC CCGCCCCACG GCCGGGTAAA CAAGCCCCGG 60 CCGCCCAGCC AAAGCCCCGC CGCGCAGGGC TCGCCCTGCT GCGGTGAGGG CACGCAGTGG 120 GAAGGGGCGC AGCGGGTGCA GGACCCCCGC CGGCCTTTCC CGGGGGGTCG GGGGAAGCGG 180 GGTTTGGAGG CGCTGCTGAG CTGTGACGCA GGCGGCCTTG GGGCAGGTGG AACCACCCGG 240 AACCCCGCAG AGCCAGGCCA ACCCCCAAGC CCCAGTCCCC ACTCCGATTT AAAGCTGCTG 300 CACAGAAGAC ACAGCACGGG CTCTGGTCCA GACTGCGGGG TGCGGCCTCG TTCAGGAGAC 360 GCCACCGCTC TGGGGCCTCA TCCTAAAGTG GGCCCACCAG TAACCCCAGT CGTATAGGGC 420 TGTAGTGAAG ATTAGATGTG TTAAGCCACG GAAAGCATTT CGATCAGTGT GGTACACAGT 480 GAAGGCAAAT AAGCCTGAGT TAAATCAATG AAAAGCCCAG GGAGCGTAAA AGTCTGCGGC 540 TCCTAACTCC AGTCTCCCCA GCCTGGGTGG AGACAGCTCC CACTCTGCCC CTGGCAGGGT 600 GTTAATGAAT CTTGTCTTGT CTCAGGCAAT CTTCAGCAGG GCCCTGTGAG GTTAGGGCCT 660 CATTTTTATA GGTGGGGAAA GTGAGGCACA GAGAGGTTGA GGGCTTTGCC CTGGGTCACA 720
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