Tag | Content |
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EnhancerAtlas ID | HS067-05757 |
Organism | Homo sapiens |
Tissue/cell | GM18522 |
Coordinate | chr5:142356550-142357750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr5:142357212-142357225 | AGCAGCTGTCTCT | + | 6.32 | NFAT5 | MA0606.1 | chr5:142357619-142357629 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr5:142357619-142357629 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr5:142357619-142357629 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09220 | chr5:142352975-142359932 | CD14 | SE_20025 | chr5:142348657-142359928 | CD56 | SE_22391 | chr5:142348639-142359898 | CD8_primiary |
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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 |
GH05I142976 | chr5 | 142355818 | 142359764 |
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Enhancer Sequence | TCATTGGCCT GGGCCAGGTT CTGTATTCAT CCCTAAAGTG GTCACTGTGA CTGAGGCCAC 60 TCCTGAGTCA TATGCTAGCC CTGGGGTTAG CTCCGCCCAA CCACACAGAC AGAGCTGAGG 120 GAAGGAGTAC ACTAAAGGAA AATTGAGAAG TTTTAGTTAG AAAGTGGGGA TGGATTCTGG 180 GCTGGCAGAA AGAACAGATG TTCCTCATAA TGAGCAATTG CAAGGGCTCA TACAAGACAA 240 GTTTCAGAGG GGCTATTGAT GGTGTGGGTA AAGAAAATTA TATAAAAGTA ACACCTCAAC 300 CCGCGGTTCT TCCTTGAGAT TATGGTTCCT TTTATTTCAC AATTTGTGGC ATTGCTGGGC 360 CAATAAAGAG AACTTCAAAC AGATATTCCA CATTCTTTTA TTGGCACACA GAGGGCCATC 420 AATTAACCTT ATTAAAAAAA AAACAACAGT GGAAGAATCC TGTTTTGAAA TCTTGATTTG 480 CTTTAAAAGC ACGTAGATGG TTGTTGACAG ATTTTTGTTG GTCCTGGGGC TGCCACAGGT 540 CAGCCAGGTG TTTTTTTCCC CCTGCTGGAT ACGGATCTTT GGACATTTGC CTCCAGTCTT 600 TGCGTTGAAC TCAGCAGTTT CCTGGGTGAG GAGGCAACCT TTGTGTGCTC AGCTTCTTCC 660 AAAGCAGCTG TCTCTAGAAG TTGCTAGCCA TCTCCTGGTT AAGAAAGAAG ATGGAAGGTG 720 GTAGGGAGAG GAAGCAAAAA CATTTCACAC TGCCTCCCCA AAGACAGATC TGTTATCCTG 780 CCTTGACCAC AAAAATTCAC GGAGGAAGTC AGTGAGTCAG AGATGCGCCA GGGTGTAAGT 840 TGTCAGCACA GTTCAGCGAG CTCTGGTATC TTGTGTTTCT CTGTTCGTAC CACTACTGCT 900 TTCCTTCCTG GCTACATTCA CCAGCATGAA GAAACTGGAG CAGCACCTTG AGAGGTTTCA 960 TCAGCCCATG GCTGGGATGG TTGACAGATC ACTTGCAAAG CCATGGGAAA AGGACCTGGT 1020 TCCTCTTGAC TCCTCTGACT TATTTTCAGT GATCCGACAT CTTGAAAATA TTTTCCATTT 1080 CACTCCTAGG TTCTTGTAGG CCTTCCCACA ATGAGCACAT TCAGTCTTAA AAATTTTTTT 1140 TCTGCTTTAA TTGGCGTGGG GTCGGATCGC TTCTCCTTGG GTCTTAACTG TATTCAGAGG 1200
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