Tag | Content |
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EnhancerAtlas ID | HS187-14766 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:231658290-231659990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr2:231658478-231658493 | TTGTTGAGTCAGCAA | + | 6.01 | MAFF | MA0495.3 | chr2:231658478-231658493 | TTGTTGAGTCAGCAA | - | 6 | MAFG | MA0659.1 | chr2:231658475-231658496 | ACTTTGTTGAGTCAGCAAAGT | + | 6.1 | MAFK | MA0496.2 | chr2:231658476-231658495 | CTTTGTTGAGTCAGCAAAG | + | 6.31 | SP1 | MA0079.4 | chr2:231659396-231659411 | GAAGCCCCGCCCACC | + | 6.7 | SP2 | MA0516.2 | chr2:231659395-231659412 | GGAAGCCCCGCCCACCT | + | 7.03 | SP4 | MA0685.1 | chr2:231659396-231659413 | GAAGCCCCGCCCACCTC | + | 6.85 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_36475 | chr2:231657688-231662098 | HMEC | SE_64504 | chr2:231657231-231662110 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 231658439 | 231659623 | chr2 | 231658746 | 231658958 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I230792 | chr2 | 231657248 | 231661845 |
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Enhancer Sequence | TGACTGAAGG AAAAAATAAT AATTCTCTGT GGTCTTATTT CTGTTCTCTA GGATTTAAAA 60 AAGTTGAATT TCATTGAAGT ATCAGTTAAG TTATATATTG AAAGACATCT CCTTTGGACA 120 TAATACGCAC GCTGTAAGGC AGTAAAAGCT GCCTCTTAAA TGGAGCATGG ATTCTCTACA 180 GCTTTACTTT GTTGAGTCAG CAAAGTACAT GTTTATGAAG TAGTGTCCTT TGATTTTTAC 240 CTCTCTGTGT CCACTTACTA ATCCATATAA TTTGGTAATT CACAGTGCAT CTTCCTGAAA 300 TTACTACTGG TCTAAGCAGG CATTAATGTT TGGGTAGTCT TGTCAGTTTA AAAAAGCCTG 360 AAAACCGAAC CATAGAACCA AATGCCCTTC TCCCTCATCC CTGAGCCTCA TTGACTGGCA 420 AGGTAACCTC CTGCTGTTTC ACACCAGAGT TGTGTGCCAG CCCCGGGTAT GGTGTGCATC 480 TGTTTGTCCC AACATTGGTG GTGGTCTGTT CTATTAAGTT GGTGGGCAGG CATGTTCCTG 540 GCATGACTGT TGGTGTGAAT CAGCTTGCTC TACTCCTCCT GGCTTTATAG CTTGCCTCAG 600 TCTGATTCAC GTCTCTGCGG TTTAACACTT CCCCCAAGTT CAAGCTTGTT TAGACAAAGT 660 GTGAGTCAGT GCCTGTGTTG CACGCCAGCG TTCTGTTTCC CTCTTTCTAT TTCTAACCAT 720 CTGTGTTACT TCTTCAGATT TTGGGATACA GAACTTTTGG CATCTAATTT TGTGTTGTAT 780 CAATTCAGAG TTGTATGTAA AAACATGTAG TGAGCAGTGT GAAATTGTGG TGATCTTAGA 840 GCAGCTTTCA GGTGCCTTTG TGTGTTTTTA AAGCCCATAT TTCCTTTTCC ATAGAAACCA 900 AGGATTATTA AAATCAATAC ATTAGTTAAC TCTGCTGACA TTTTTCACTT CAGAGTAATC 960 AGAGGCATGA TATGAATGTT GTTAAATGGC ATGTCAAGAA AGACTTTTGA GATACAATTT 1020 ACAGTTTAGA GCTCTCACCT GTGCTGGCCA GAGCAGACAC TTCCAGCCAG GAAGTAGCAT 1080 GGAGAATGCA ACTGGTGGGC CCACCGGAAG CCCCGCCCAC CTCCTTTGTT GTGAAAAATA 1140 TACGTACAAC TAGAGGGAAT ATGTAACATA CCGGTTCCTA CCCTAAACCC AGCTTCAACA 1200 GTTACGAATG TTCTGTCATT CTTGTTCCTC TAGTCCTTGC CCCCTTTTTC CTCTGACACA 1260 TGACATCACT CAGTATGCAT CCCTAGTACG CATTACAAAA CACAGTATAA CACAGTTACG 1320 TTACCATTTG CAAACCTAAT GTCTAATGCC CAATCTACAG ATTTCCTCAA TTTTCACAAA 1380 AATGGCATTT TACAGTTCGT TTATTTAATA TTACTTCCAG GCTGGACATG GTGGCTCACG 1440 CCTGTAATAC CAGCATTTGG GAGGCCAAGG CGGGTGGATC ACTTGAGTCC AGGAGTTTGA 1500 GACCAGCCTG GGCAATATGG TGAAACCCCG CCTCTACTAA AAATACAAAA ATTAGCCGGG 1560 TGTGGTGGCA CACACCTGTA ATCCCAGCTA TTCGGGAGGC TGAGGCACAA GAATAGCTTG 1620 AACCCAGGAG ATGGAGGTTG CAGTGAGCCG AGATTGCGCC ACTGCACTTT AGCCTGGGTG 1680 ACAGAGCAAG ACTTGATTTC 1700
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