Tag | Content |
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EnhancerAtlas ID | HS006-08234 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr11:129731410-129732640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr11:129731420-129731430 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr11:129731420-129731430 | GGCACGTGCC | - | 6.02 | RREB1 | MA0073.1 | chr11:129732499-129732519 | CCCCTAACCACCCAACAACT | + | 6.32 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_27353 | chr11:129731037-129732709 | Esophagus | SE_27846 | chr11:129730398-129732763 | Fetal_Intestine | SE_35121 | chr11:129730409-129733029 | HeLa | SE_36539 | chr11:129730682-129732779 | HMEC | SE_57651 | chr11:129732057-129732417 | VACO_503 | SE_64293 | chr11:129730399-129732758 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 129731556 | 129732597 | chr11 | 129731747 | 129732130 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I129860 | chr11 | 129730176 | 129732734 |
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Enhancer Sequence | AGGGCGTGGT GGCACGTGCC TGTGATTGAT CCCAACTACT CAGGAGGCTG AGGCAGGAGA 60 ATCACTTGAA CCCAGGAGGC GGAGGTTGCA GTGAGCTGAG ATCTTGCCGC TGCACTCCAG 120 CCTGGGCTAC AGAGTGAGAC TCCATCTCAA AAACAAAAAC AAAAACAAAA CACTCACCAT 180 AGCTGTGCCA TTCATCTATC AGAAACCTGA AGCCAGCATA TGAAGGAAGC AAGTGTGGCA 240 CAAATCCTGG GCTGTCACCG TAAACAGCTC CAGTAGGAAG TTCCCATTCT CCGCTATTGC 300 CATTCCACCC ACAGGCTGGA TAGTGCCGAA GTTACACTTC TGAGGAGTCA GCATCCTGAC 360 GCAGCCTAAA CTTTACACTC ACTCCCTGCT CTCCAGAATG CACACGTCTG CCTGTGCAAA 420 AACGACAAGC AGAGTCAGGT GACCTCAGCT AACAGGAATG TGGGCAGGGC TGCGGCTGAA 480 TGCCAGAGCT ACTTTTATTA AATTCCTTGT TAAGTAAATT CAAAAGGGGT TTGTTTGTAG 540 CTGGCAGTAA ATACCTAAGA CAAGATCTCT GGAATTTCTA CCTTTTTTTT TTTTTAATTT 600 AAAAACTGTC ACATGGCTTT CTATGTGAAA TGTGATTCTT GAAAATAACA GATACGCAAA 660 TATCAAAGGA TTATCAAACG CAGACACACT CGCCTTTCTC AGGTGGAAAG GCCCATTTCC 720 CCGCACTGCA TCCTACCTCT CCCCACTGCC AACCTCATCC CGTGCCAGTC TACTTGCCCA 780 TCACAAGCTC AACCTGGGAG GCCCATTCAC CTCTGCTCTC TGCAATGCAG GCCTCCCACC 840 TCCTAAGACT GGATCGCCCC CAGGCTCGCC AGGATACATC ACAGCCCTCC TGCCCGGAGG 900 AAGGCAACAG AGAGAGACTT GACTTAGAAT CAGAAGCTTC TCTTTAACTT CAACTCAGAC 960 TCATGTCTTC CAACGGTTAA AGGGGAATGA TGACACTGAT TTTACAAAAT TGCTCTAAGA 1020 ATTAAACAAA ATGTCTGTGA AACAGCTGTG GAGCCAACCA GCCTCCCAGA CCCTCCTCCG 1080 CTTCGCAACC CCCTAACCAC CCAACAACTA AGCCAGGCTG CCTCCATCCC ACATCCTTCA 1140 GCTCCACCTC TTCAACCCAC AAGAGCTTCA ATACACTCCA AAAATTAAAG ATACTTTTTT 1200 TTTTTGAGAC GGAGTCTTGC TCTGTGGCCC 1230
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