Tag | Content |
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EnhancerAtlas ID | HS061-16739 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr22:38558130-38559430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr22:38559097-38559111 | ATTCCCCAGGGACC | + | 6.84 | IRF1 | MA0050.2 | chr22:38558240-38558261 | AAAAAGAAAGTGAGAGCAGTC | - | 6.27 | IRF1 | MA0050.2 | chr22:38558234-38558255 | AAAAAAAAAAAGAAAGTGAGA | - | 6.77 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27733 | chr22:38558110-38562572 | Fetal_Intestine | SE_28874 | chr22:38556949-38562636 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 38558200 | 38559288 | chr22 | 38558947 | 38559326 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I038161 | chr22 | 38557803 | 38562790 |
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Enhancer Sequence | GCTTGAACCC CGGAGGTGGA GGTTGCAGTG AGCTGAGAGT GTGCCACTGC ACTCCAGCCT 60 GGGCAACAGA GCGAGACTCT GTGTCAAAAA AAAAAAAAAG AAAAAAAAAA AAAAAGAAAG 120 TGAGAGCAGT CAGCAAAAAG GTATGTTCCC CTAGCCATGG TGGAGAACTG AAACCAAGCA 180 GTTCTGGGGT GGTGATGCCA GGATGACGAA GAGAGAGAGA AGCAAGGAGG CAGGAAGTAT 240 AGGTGAAGGA GTGACAATGA CAGGCCATGG AGTCCATGCT GGGTACAAAG CAAGGCACAT 300 GAACGGGATG GGGCTGGGAA AAGCGGCCAG GAGCAATTCC CTGTCAATGG GGAAAAGCAC 360 TGTGTGGGTG GAGGACTAGA GGGAATGAAC TGGAAAGACA GAAGGCAGAG ACTGGAAAGT 420 GGGGTGCTTG AAACTTGTAT TTACGGGAGA GCTGCTGTCA CTGGCGATGA TAAAGGCCAG 480 CGCGTGGTCA TGTGAATGTG GAGGGTCAGG AACCAGAGGC AACGCTGAGT CAGGGGCTCA 540 CATCTTTGAG GATGTGGGGG AGCACCCCAG GCTCGTAGAT ACCTATCACC GGGGTGACAG 600 CAAGTGGTAT TGTAGGGTGA CAGAAGATTC AAGGCTGGGG GCAAGGAGGA CCCTACCCCA 660 CCTCCAGGCC CAGTGGGAGA GGGACTGGGA GAGAAAACTC TCAGGAGGCT GCGGGGCAAG 720 CGGGTCCTTC AAGGAGAGCC AGGTGTGGGT TACAGTGAGG AGGCAAAGGG GAGATTCAGG 780 GAGAAGGCTG AGGCTCTGGA GGACACACGG GGGTGTGTCT CTTCCCTCCC TTCTAGAACC 840 CCAGGCTGAA GCCACCTGGC CTCCACTCAG AAGCCTCTGC TGTGTCTCTG CTGGGGTGGG 900 AGGGGTCTGT GGCTAAGCCT CAGGGGACCT GCAAACCTCT TGAAAGTGGC TGTGTGAGCC 960 TGTTCTCATT CCCCAGGGAC CTCAGGGGGT CCTGGACCAA AAAAAATGCC AAGGACCCTC 1020 ACGCTAGAGC AGTACCTGAG TCCCCAGTTT CAAAGCCCAG CACAGGCCCT TCCTGCCCAC 1080 AGGCTCCCCA CAGGGCCCCT CCTCTGTCCT CTGGGCCTTT CCTAGTACCT TGTCTCTGTA 1140 GGGCCTTTCC CTCCAGCTGG TGGAGTCTTC TGGACCCCTT AAGGTCTATC TCTACCCCAG 1200 CCACCCCAGT GGAGCCTTTC CCACGCCCTC TGGTCAACAC ACTTGGCCTT CAGCAACCAT 1260 GGATACATCT AGCCACTCGG CAGATATTTA CCGTGCACCC 1300
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