Tag | Content |
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EnhancerAtlas ID | HS089-07223 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr2:28583720-28584820 |
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) |
MAFF | MA0495.3 | chr2:28583982-28583997 | GGGCTGACTCAGCAC | - | 6.05 | MAFF | MA0495.3 | chr2:28583982-28583997 | GGGCTGACTCAGCAC | + | 6.08 | RARA | MA0729.1 | chr2:28584729-28584747 | GAGGCCAGGAGGTCAAGG | + | 6.13 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_20015 | chr2:28580994-28584412 | CD56 | SE_22508 | chr2:28581176-28584226 | CD8_primiary | SE_34659 | chr2:28581009-28584958 | HeLa | SE_51112 | chr2:28583810-28584935 | Skeletal_Muscle | SE_62927 | chr2:28581266-28660518 | Tonsil | SE_65553 | chr2:28582948-28584730 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 28583784 | 28584228 | chr2 | 28583781 | 28584578 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I028358 | chr2 | 28581236 | 28585206 |
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Enhancer Sequence | CCACACAGCG GGGAGCAGGT GGCAGCACGG ACGCTCGAAG CTTGGTCTCT CGCTGTGGAG 60 TTTTCTCTCG CCTGTCTCTA CCGCTATCAT CCTAATACTG AAGCATCAGG TCCTTTTTCA 120 AGACACCACC AGCTACAAGC AGAGGGCAAG CCTGGGGCTG AGAAGCACTG TGGGGAGGAG 180 GGGTGGAGCT GGGAGAGGGT CACGGGAGTC AGGGGCCAGG GAAAGCTGCC AAGCAGAGAC 240 AGCCTCTCCT GCCCCTTTCC CAGGGCTGAC TCAGCACCTT ACGCGTGAGG ATTTGTCATC 300 AACAACTGAC CCCAAAAGCC ATGGTGCCCT GGGGTTGGTG TCCCAGTGAT GCTTTTCTGA 360 CTCGTGGCCC AGGATGACAC AAAGCCCCAA GGGACAAGCC AGAGATCCCA CTGGCCCAGC 420 CAGATGCTCC AAGATTCCTT TTGCCTGTAA CCCAGAACTG GCCCACCCTC TTGCCTGGTT 480 ACTGGGGCTT TCACGAAAGA GCAATGGACA GTGGGAAGGG CTCGCTGTGA GGCAGGATCA 540 GTCCTGGGGC CCTGGGAGTG TCTCTTCCCT TCCCCGAGCC TCAGTGTTCT TGTCTGTACA 600 ATGGAAGTTC AGGTCAGATG GTCTCTGGAT TCCTTCCCAG CTCTGAGAAC CAGGTTCTAC 660 CTCAGCTGTT CTCAGAAAGG ACAGGGTGGT CCGGGCTGGG CATGGGCTTG AGGCTTGTGC 720 CCCTCTCCTA GCCCCAAGGA CTTCCCATCC TTTCAGGTCC CGCTGGGGCT CAGCTGCCCA 780 ACTCTGATCA GAAAGAAGAG CTGTAAGTCT GGCTGGGCGG TGGCTCATGC CTCTAATCCC 840 AGCACTTTGG GAGGCCAAAG AGGATGGACT GCTTGAGCCC AGGAGTTCGG GACCAGCCTG 900 GGTAATGTGG CGAAACCCTG TCTCTACAAA AAATACAAAA ATTAGCCAGA TGTGGTGATG 960 TGCGGCTGTA GTCCCAGCTA CTCAGGAGGC TGAGGTGGGA GGATCACTTG AGGCCAGGAG 1020 GTCAAGGCTG CCATGAGCTA AGATCACAAC ACTGCATTCC GGCCTGGGTA ACAGAGCAAG 1080 ACCATGTCTC TAAGAGAGGG 1100
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