Tag | Content |
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EnhancerAtlas ID | HS081-16144 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr5:150998980-151000410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr5:151000297-151000312 | CCTTTCCTGAGAAGC | + | 6.25 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_26617 | chr5:150998299-151003490 | Esophagus | SE_33777 | chr5:150996068-151001541 | HCC1954 | SE_36199 | chr5:150991861-151001529 | HMEC | SE_64237 | chr5:150991708-151001277 | NHEK |
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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 |
GH05I151612 | chr5 | 150992051 | 151001367 |
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Enhancer Sequence | GTGACATGAT GTGTCCAGAG TCATTCAGCT CACAGGTAGT CAGAAAGAGT CCCCACGCCT 60 CCAGGATCCT GGTGTTTCCC TGACACCACA TCCTGAGATG ACTGACAACT GGTCAACTCA 120 TGTATTGTCC AGGAGCCATG GAGCCATGTG ACAAAGTAGC CTGAGGGACC CCCAAGAGAC 180 CACTGGTTCC ACACTTTACC TCCATTGTTG TGTTAGAGCT TTATACCCTG TGAAGAGAGC 240 AGGCCCAGAA ATTGAGAAAA CCTGCATTTG AATCCACCTA ACTAGCTGCG AACCCAACAA 300 ATGTCTCTTT TCTGGGCCTC AGTTTCCCCA CCTGCAAAAG GAGTTAGTTG GGCTCAGTGA 360 TACCTAAAGA CACTTCTAGC TCCAGCTTGG CCACTGTCTC AGGTTCCAAG ATTTCCCCAC 420 CCCTTGTGGT AGCTTCAGAT TTCTTGCCTG GGGGAAGAGC CAGGGCAAGT TGCTGCAGTT 480 CTGTTCTCTC CACACAGCAG AGTGGCGGCT CCCAGCCCAG AGTGGAGGCT TACCTAACCC 540 CAGCAAGCTG AGCAAATCCC TGAGAACAAA AGGGGGAGAA GACCTGACAA GGGAGGGGAA 600 GGAGTGAGTC TATTCCTTCC TTGCACAGCA ACTTTAACCC CTTCCATGCC TCCCCAGCAG 660 CAGGAGGGCA GGCAGGGTTT CCAGACAGGG GGTAATGAAT GCATCTCAGG CATGCACGGG 720 CTTCCAGGAA CTGCTGTGCC ACCAAAGCCA ACTTTCCATA GGGGAGCCCT CCCTGGGAGC 780 AGCCACAGCT GGAGATGCCA TTTGTCCTTC ATAGACCCAG ACTCATGGCA TCAAAGCCCC 840 CCACCGCTCC ACCCCCAACA AAAGCCAGAA GGGAGCTGCA TTCCATCCTT CTGCCAGTCA 900 GGAAGCTGAA GCCTAGAAAT GGGGAGGAAC TTGCCCAAGG TAACATAGCT TTCGACTCAC 960 AGGAAGGGGC CTCGACTAGG ACAGTGCCAG ACACAGAAAT GAATAAAGTG TGTTCAATGA 1020 CCGGAATCAA GGCCTCCCCA CCTTGCGCTC CTTCCTCTGT GCATACTATA TTGCCTTTTG 1080 GGATTCTTAA ATCAAAGTTT CCATCCCCAA ATTAGAAGCA GATTGTTGAG GCCTGTCCAT 1140 AAATTCCTCA CTTGAACCTG TAGTGACTAA TTCTCTCGGG AGTGTGGGAT CAAACCCACC 1200 ATGGCTATTA AGAATTTAAT ATGAAGCCCC AGTGCCTGGG GCCGTGCTTT CTCATCAGCC 1260 CCGAAACAGG GCGAAGCCTG CATGTCAGGC GGGGCCAAGA ATGCAAAGTC TGGAGTCCCT 1320 TTCCTGAGAA GCTTCCTGGG ACAGCAGCCT TCCCTCTGGG GAAATTCTCA GGGGACCTTC 1380 TGAACAAGAA GTGTCTTTTT TCCTGCACCA GTCCTAATCA TAGACAAAGT 1430
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