Tag | Content |
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EnhancerAtlas ID | HS038-00222 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr1:19227620-19228950 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:19228574-19228586 | GCTAAAAATAGA | + | 6.92 | MEF2B | MA0660.1 | chr1:19228574-19228586 | GCTAAAAATAGA | + | 6.44 | MEF2C | MA0497.1 | chr1:19228572-19228587 | GTGCTAAAAATAGAA | + | 8.55 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_26830 | chr1:19228361-19230663 | Esophagus | SE_47330 | chr1:19227817-19231739 | Panc1 | SE_53460 | chr1:19228446-19230083 | Spleen |
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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 | CATCTTCCTG AGTCTCAGAG TGCAGGGAAG GCCTGCAAAC GGGATCACAC AGGGAGTATG 60 GCAAGTGTGG CCCCAGTCTC AGCCTAGAAG AGGAACCCCT CTGTCCCATG TCCTCTTCCT 120 GCGCCCTTTC CTATCCCCTC TTCACCCACA GAGGACACAC AGCAGTGTTG CAACTCACTT 180 GTGCTCAGAG CACCACCATG CCATCCCTTG GGGGAAGGGA GAGGGCCACT GATTAACTCA 240 GAAAGGGCAC AGCTCATCAG GAAAGACACT GCCACTAACA GCCCCAGGGG TCAAGCAAAC 300 AAACCTCAAA TGGGAGGGGG GGCTGATCCA CAGGTGGGCA GCCCCACCAG ACTAGGAACC 360 CCTCTGGGGC AGGGTCTGTG TCCCACCTAC CTCTCCAAAC CTAGCTCCGA GCTGGAGGGG 420 CTCTGAGAAT ATTTGTCATT GAGTGGGCAA GGGTCCAGGC ACCTGGCTCC ACAATGTCAG 480 GTTTGCAAAT CGGGATTTGA AGGGCAGGTC CACCCCTGAA CTGCTCCTGG GTTTCTTCAT 540 TATTTGGAAT AATGACCTGC CTCACAGGAG TGAGAAGTTT AAATAGAGGT GATAATGATG 600 ATGATCGTGG CAATAATAAT AACCGGGCGC TGCCTTTGTG CTGGGCACTG TTCAGTGCAC 660 TCCCCATGTA TTAACTCATT TAATCCTCAT AAGACACCTG CCAATTGCCC GGCCAGCATT 720 TGGTTCATTA TAAGCACTCT ATAAATATGA TTATTCCACC TACAAGAAGA AAGGAATCCT 780 TTTTTCTGTC CAACATTTAA CTTGAAAAAA AAAAAAAAAA ACGGGCGGCG GGGTGTGTGG 840 GGAGCGGAAA AGAGAGAGGT AGAAATCCTG GTAGAAGGAG AGGACTCGGG GAATCCGGGG 900 CGGGATGGGG ACACTGAACG TGAGACGAGG GTGGGGAAGT GAGATGTGTG GTGTGCTAAA 960 AATAGAAGGG CCCCTCAGGG GAAGCCAGCA AATTGCGAAG ATCCAGTATT AGGAGTGAGG 1020 TGAGTGACTA CAGAGGCTAC TTTCCGAGCG TGGGAACCGG CAGGGCCACC GAGGCACCCT 1080 ACTCGGTCGC AGGATTCGGG AAGAGGGGTC CCCTCGCTAA AGGAAGGTGA CTACCTGAGG 1140 GAGGAGGCTA AGGGATCTCA GTGGGAGAAA GGCCTGGGTG GGGGTCGGAG GGGAGCCCCT 1200 GAGGAACCCG GCGTTGACCG AGGCAGCTTG GGGGTCCGGC AGGGAGGGAG TGCGGCGCGG 1260 GGGACGCCCA GTGACTCTCA GGCTCCCGGG CCCCAGGCGC GCGCTCGGGC CGCCCCGGGC 1320 CCCGTGCTCA 1330
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