Tag | Content |
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EnhancerAtlas ID | HS187-18235 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr4:2291360-2293530 |
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) |
ELK4 | MA0076.2 | chr4:2293267-2293278 | GCCGGAAGTGG | - | 6.62 | Gabpa | MA0062.2 | chr4:2293268-2293279 | CCGGAAGTGGC | + | 6.62 | PLAG1 | MA0163.1 | chr4:2292280-2292294 | GGGGGCCATGGGGG | + | 6.02 | ZBTB7A | MA0750.2 | chr4:2293266-2293279 | GGCCGGAAGTGGC | + | 7.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_55288 | chr4:2291500-2293949 | Thymus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 2292802 | 2293042 | chr4 | 2292648 | 2292996 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I002290 | chr4 | 2291910 | 2293925 |
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Enhancer Sequence | CCAAAGCAAT GGGATTACAG GTGTGAGCCA CAGCACCTGG CCTCACCTTC CCATTTTACA 60 GACAAGTAAA CTGAGGTGCT GGGAGGTTAA GTTCCCTGCC CAGACGGCAG AGGTGACACA 120 GCTTACCACA GCCTGCGGGG GCCTGTGCAT CGTGCTCCAG GACACTTGTG GACTTGGGGC 180 TCAGGAGGTC CCAGAGATGT CTCTGGTCAG TCATCACGGT GGTGTCCAGA AGAACTCGGC 240 GAACCTGAGT TCCCCTGAGC CCCCGATCCT CATCACCCAC AGGGGACAGC CAGGCTGTGG 300 CCAGCACTCC TCACCCCAGG GATGCTCTGC AGAAGCTCAG GGGGAGGACA GACACAGACA 360 GACAGTGGAC AGGCCCAGGG AGCCGCTGTC CTTGCGGAGG CCAGCCCAGC TCAACAACTG 420 ACAGACAGCC AGGCCTCAGC CAGCAGCGTG ATGGCAGGCC CCGTCAGAGC CACCCCCCGG 480 TCACCAGGCC CCCAGCCTGT GCCCCAGGGG ACTCACGTGC AAGATCTCCT CAGGGGACAA 540 GGCCGCCCAT GCTGGCAACC CGGAGCCCAG AGAGAGCAGC CCATATGGGG ATGGCCCGGC 600 AGTCCCCAGG ACCATGCCAC CTGGAAGGTG TGTGACCACA AGCCTGCCTG CCTTCTCCGA 660 GGAGCTGGGG TCTCCTCAGC TACAGAACAG GGTCTCGAAC TCTTGGCCTC CCAAAGTGTG 720 ATCCTTCAGA GGATCACAAT GTGCCTGGTG AGACAGGCAG GTTGCAGGCC CCAAGGGCCA 780 CTTTGCCAGT CGTCATGGTG ACCCCTCCAT GATCCCGTAG CTACCCTGAC ACTCCTGTCT 840 GTTGGCCCTC TCCAGCTTTG TCCTCTCGTG AGGATGCAAC GCTGCTCACT GATGGCCCCC 900 AGGAGATGTC TCCAAAAGCC GGGGGCCATG GGGGCAGGTG CAGCAGAGCA GGACACGACC 960 ACACCTGCCC CCTGGCCCCA GAGCAGCTGC TGACGTCCAC GGCTCACCAG GTCCTTCAAG 1020 AAGTCAGCTC CTCTGGGACG GCCTCACCCC TCTCCTGCTG TGGGGCAGGG GCCAGGCCAG 1080 GGCTGGGCCA GGGGCCAGGC ATCGCCTTGG GGTGCTCACC TGGCTCCTTG CTTCCCCTAT 1140 TAAGTCCAAG CACAAGCCGA GCAGTGGTGG GGAGGGGTGG GGGCCATAAT CTGGTCCCTC 1200 CTGGCCCAGC CCTGCCTGGC CAAGATCTGG ACTCTGGGGA CACAGTGAAG CCCAGGCCTA 1260 GACACAGCCC AGCTCTTGAA AAGATCCCAC TATTATTATG GTCTGGGAAA CTATCCCTTT 1320 ATGTTTTTCT TCGTAATTAC ATAAGCAATA CATGTGCACC CTAAAAAAAT GAGGAAATGC 1380 AGATTAGCGA AGAGTGCCTG CACGTGTGCT CCTGCCCCCG GCACACGAGC GGGAGGAGCT 1440 CCTGTCGCCC TTCTCGTCTC GCACCTTGCA GGCGCTTTTG CTGCTTTAAA AAGCTCTCTG 1500 AACAGAAGCC ACCACAACTG GCGAGTCTCA GAGAGGTGGG TGAAGTCAGC TGAGGACGGC 1560 ATCCTGGTCT CCGGCTGCAG CATCACCGCG GTTGAAACCC GCTTCCTCTT GCTTTCGGCT 1620 CAGTGAAGGT GGGAGGAGAT GCTTGGCTTT CGAGAAGGGG CTGTTCCCCC TGGAATTTTC 1680 CTGGTCCCAT GGGGTGGAGG AAAACGACCC CTTGAGAATG CTTCCTGGAG CCACTGGGGA 1740 GCAAGTGGCT GGCACCTTCT CACCTTCTTG GGCTCACGGG GAGGCCCCAT CCCCTTCTAG 1800 GCTCCCCGAG GAGGGGCCAA TGCTTACCAA GCAGGCTCCA CTGCAGCCAA AGCCCCCGCT 1860 TCCACCCCTT GACGGGCTCC CTGATGCTGC CAGGAGCAGG GAGTAGGGCC GGAAGTGGCC 1920 CTGAGTCCCC TCTCTCTCCA CCTCAGACAC TGCTGTGTGC CTCACTGAGA CCTGTCCTGA 1980 GGGACAGGGC TGGGGGTCCT GGGGTCAGGA GAGCGGGAAC TGAGAGCTGC ACCTCAAGGG 2040 GCAGCACTAC AGGCCTGGAC TCTGCCCAGC TCCTTCTCCT GGAGCCCCCC TCGGAATGGC 2100 AGCCTGCCAC ACTTGCCGAT GCCCATCCCA CTCCCCACAC GCCTGGCTGG TGGAGGACAT 2160 GAACCCTGCC 2170
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