Tag | Content |
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EnhancerAtlas ID | HS087-09915 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr18:28786050-28787570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr18:28787555-28787570 | GGTTAATAATTAGCA | + | 6.05 | HNF1B | MA0153.2 | chr18:28787556-28787569 | GTTAATAATTAGC | - | 6.02 | SOX10 | MA0442.2 | chr18:28786064-28786075 | AAAACAAAGCA | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28330 | chr18:28782024-28789597 | Fetal_Intestine | SE_29124 | chr18:28781818-28789503 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I031202 | chr18 | 28782183 | 28789344 |
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Enhancer Sequence | ACACATTGCT TTATAAAACA AAGCAGTAGA CTGAAGAAAT GCTGAATGGT GGCCTTGATT 60 ACTACCTCAT TGTGCCTTTG CACAAGTGGA AAGGCTGGGC TTGGAAGTCA AAAGACTTTA 120 ATGTTAGTTC TGCTAGCTAT AAACTGTATG ATCCCAGCAA ATAACATAAC CACTGTTGCC 180 TCATTTCCTC TGTCTGTGAA ACTGGAATTA TACTTCCGCC TCTATGACTT TGAAAAGATA 240 TGGGAGGTAA CTGCACAAGA GAAAGCACCT CACGTAAAAC CTAAAAAGCA ATAACAGCTC 300 TCCTGTAGGA AGTATCTACT GTGTGCTGGC TATGTTACGT ATTTCGTTTA ATCCTTATAA 360 CACCCCCTTT GATAGGTATT ACTTTTCACT TCCTACAGGT GAGGAAAATA AGGCCTAAAT 420 AGGTTAAGTA ACTTCCCTGA AGCCCCACAG CTTTGCCACT TAGCCAAGAT TTGAACCCAG 480 TTCTAGCTCA GACCAACGCC ATGCAAGCTT TTTGCTCTAA TGCCTTTTCC CCCTTCCTTT 540 CTCTTTTTGG CACACCAACT ACAGACTGCA ATAGGTTTTA ATTTAAAATG CCTAATAAAA 600 ACATACTTTT ATCAGAAAAA GCTACATACT TATATATGTA TCATGCACAT GATTACATGA 660 GCAACACATA TTCGCAATAT AATTAATTCA AGTAATAATT CTGTCCCACC CTGATATTAT 720 GTATGTCCCA TTTCCGATAC CATCTTCTGT GTTCCAGAGA TGAGCAACCT TGCTTGTGCT 780 TGCTCAAGCG AAACACAGTC AACTGCTCCG GTGTCACTCG CTCCTCAAGT GGCCTGAAGC 840 CGTCCAGCGG TCTCGGTGAG TAATGCAGTG ACTAAAGCCC ACACAAAAAG GAAGCAGTGC 900 CCTTTTAATA GAGCCACAAT ATAAAGAAAA CACTCAAGCC AGTTCCAGCT ACTGTGAATG 960 ATTTATTGGG TGAGCCCTGC CCGACTAGGC CCAGCAATTT CCCATTTGTT GCGTCCCAAT 1020 CCTGCCCCTC CCACATCTCC ACCCTCCTGC TGCGGGCCCT TCCCAGGCAC CTCCCTCTTT 1080 TTATGGTGAC TGCAACTCTG CAGCTAACAG CTCACACACC ACACCCTGAC TCCTGCACTG 1140 GCTCAGGCTC CCTGGGATCT CTCTGCCCAA CCCTCAATCC CCTCCTTCTA CCTGCATGAA 1200 GCCTCTCATT AACGTGCCTT CCTTGACTCC TCTACAGACA CCTCCCACTT AGATTCCTCA 1260 GCCTGTCTTC TTTCATCTCC TTTTTCATTT TATAAATTCT TTCCTAATTA CCTCAAATCA 1320 CAAGCATGTC AGATTAATTG AGTAAACCTC TTGAAAGTCT GTCCTCATAG ACAGAGCACT 1380 CTGATGACAA TCTTCCTCGA AGGGACAGCT AGACACTCGG TTAGGTCAGC TCCTTAGGTC 1440 TTGCGGCAAT GCCTCATGTA AATGCTGCAC GATATCCATT CGAGTGCAGA CAATTGCCAA 1500 TTACTGGTTA ATAATTAGCA 1520
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