Tag | Content |
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EnhancerAtlas ID | HS102-02355 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr1:209977860-209979290 |
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 | CCACCCAAAT CCCAACGCCT GAAGAACCAC CTTAGCCTAG TTGAACTCAT CTTGGTATCT 60 CTAGCTGCCA TCACAGCAAA ATGTAAGGCC TGTGTCTCTA ACAGGTACTT AAACAGCCAA 120 AGGACAATGA TGCTAACCTA TCTATTCCCC TCACAGTGAG CATAGAGGAG GGACACTTTC 180 AGCCTCCTCC GAGCATAACT GTCCTCTCCC ATACCCCTAT TCTAGGGAGC AGGTCCTCCA 240 TAAACACCCT CATTGCCACC TCCATAGCTC CTCCCCAGAC TAGTTTCCAG GGGCACTGCC 300 ACACAAAAGC CGAGATTTGG CCGTCAGTGG TTTTGCTCAG GTTAAAACAC ACGCCATTTC 360 TCGCAGACAA TTCTTAGCAG TCCCAGCTCT TCCCTTTCTC CTGAAAGAAA TGAAATGCCA 420 TCGTCTAAGT TCCGTTCCTC AGGCTTCCCT GTTTAGCCCT GCTTAGGGGT AAACTGCAGG 480 CCTCTAGTCA AAATGCCCAC ACCCTTCCCT TCTGCTGGAT GGAAGCTGGG GGATGGCGAA 540 TGGGAGTTAC AAGGTATTGA GTGCCACTGT CATACATCAT ACACACGTCT CATCCTAAAC 600 CACACTCCTG GGTCAACACC AGCTTTCACC AATCCCACCC AAGCGCCTTC CTCTCTCTAT 660 CCATCTCTTT TCCCTGACTT CCACTCTTGA CATCCACCAA GAGAACAGGT TGGAACAGGA 720 TGACCCCTTT ACCACAAAGC AGGCTCCCTG TAAAGAGTGA CACCTCAGGC CTCCTTTCCA 780 AGTCAGGCCT GGGAGACTTT CCCCATTCTC CACACCACCC TCCAGCCCCT TCGGGCAAAG 840 AGGGCCCACC CCCAGAGCAA CCACACCCCA GCGCCACCCT CCCCAGCACC TAGCTCCGCT 900 CCTTGGAAAT CCAAGGTTGT CTCCCAGGCC CAGGGCGAAG GGCCTAACTG TGCCAAACAG 960 ACTCAGGGAG GGAAGACAAA CCGCCAATGC TCCAAAGCTC CTGGCCACCC TCACTCCAGT 1020 TTCCCAAAAC GCCCACTAGG ATCAAGGACC TGCGGACCTG GGAAGTCCCC TCTCTGGGAC 1080 ACAGGGGCCA GCCGCAAGTT GGTAAGACTG AAGGGGGCGC GGTGCTTTAG CTCTACCGGA 1140 TAGTGGGGTT GTTGACGGCC GAGAGCAGTG CCCTCCGCTT CGGCGGTGGG GGTAGGGAGA 1200 GTAGACACAA GTGTAGATTC GAGAGGGGCC TAGCGCTACA GAACTGAGGC CGCCCCAAAG 1260 CTATCTGGAA AAGGGCGACA GGCACCCAGC CCCAGTGGGT ACCCACCCCA AACACACAGA 1320 TGCCCCCAAG CAAGTTCTCT CACCCCCTAC AAACTCCGGG GATGGGTCCT ACCCCACCCA 1380 CGGGGGAGCC TCTCCTCCCT CAAGCTGGTC CCCAGAAGTT GGCGTACCCA 1430
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