Tag | Content |
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EnhancerAtlas ID | HS081-01776 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:209978040-209979290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:209978709-209978729 | CCCCAGAGCAACCACACCCC | + | 6.16 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27309 | chr1:209977673-209980487 | Esophagus | SE_27823 | chr1:209977468-209983975 | Fetal_Intestine | SE_35823 | chr1:209974126-209984775 | HMEC | SE_64223 | chr1:209974556-209984573 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 209978699 | 209978810 | chr1 | 209979142 | 209979287 |
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Enhancer Sequence | AGCCTCCTCC GAGCATAACT GTCCTCTCCC ATACCCCTAT TCTAGGGAGC AGGTCCTCCA 60 TAAACACCCT CATTGCCACC TCCATAGCTC CTCCCCAGAC TAGTTTCCAG GGGCACTGCC 120 ACACAAAAGC CGAGATTTGG CCGTCAGTGG TTTTGCTCAG GTTAAAACAC ACGCCATTTC 180 TCGCAGACAA TTCTTAGCAG TCCCAGCTCT TCCCTTTCTC CTGAAAGAAA TGAAATGCCA 240 TCGTCTAAGT TCCGTTCCTC AGGCTTCCCT GTTTAGCCCT GCTTAGGGGT AAACTGCAGG 300 CCTCTAGTCA AAATGCCCAC ACCCTTCCCT TCTGCTGGAT GGAAGCTGGG GGATGGCGAA 360 TGGGAGTTAC AAGGTATTGA GTGCCACTGT CATACATCAT ACACACGTCT CATCCTAAAC 420 CACACTCCTG GGTCAACACC AGCTTTCACC AATCCCACCC AAGCGCCTTC CTCTCTCTAT 480 CCATCTCTTT TCCCTGACTT CCACTCTTGA CATCCACCAA GAGAACAGGT TGGAACAGGA 540 TGACCCCTTT ACCACAAAGC AGGCTCCCTG TAAAGAGTGA CACCTCAGGC CTCCTTTCCA 600 AGTCAGGCCT GGGAGACTTT CCCCATTCTC CACACCACCC TCCAGCCCCT TCGGGCAAAG 660 AGGGCCCACC CCCAGAGCAA CCACACCCCA GCGCCACCCT CCCCAGCACC TAGCTCCGCT 720 CCTTGGAAAT CCAAGGTTGT CTCCCAGGCC CAGGGCGAAG GGCCTAACTG TGCCAAACAG 780 ACTCAGGGAG GGAAGACAAA CCGCCAATGC TCCAAAGCTC CTGGCCACCC TCACTCCAGT 840 TTCCCAAAAC GCCCACTAGG ATCAAGGACC TGCGGACCTG GGAAGTCCCC TCTCTGGGAC 900 ACAGGGGCCA GCCGCAAGTT GGTAAGACTG AAGGGGGCGC GGTGCTTTAG CTCTACCGGA 960 TAGTGGGGTT GTTGACGGCC GAGAGCAGTG CCCTCCGCTT CGGCGGTGGG GGTAGGGAGA 1020 GTAGACACAA GTGTAGATTC GAGAGGGGCC TAGCGCTACA GAACTGAGGC CGCCCCAAAG 1080 CTATCTGGAA AAGGGCGACA GGCACCCAGC CCCAGTGGGT ACCCACCCCA AACACACAGA 1140 TGCCCCCAAG CAAGTTCTCT CACCCCCTAC AAACTCCGGG GATGGGTCCT ACCCCACCCA 1200 CGGGGGAGCC TCTCCTCCCT CAAGCTGGTC CCCAGAAGTT GGCGTACCCA 1250
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