Tag | Content |
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EnhancerAtlas ID | HS052-13607 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr15:91388000-91389250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr15:91388239-91388249 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr15:91388239-91388249 | GGCACGTGCC | - | 6.02 | JUN(var.2) | MA0489.1 | chr15:91388555-91388569 | GAGAAATGACTCAG | + | 6 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_19151 | chr15:91387934-91389298 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_40123 | chr15:91388102-91389199 | K562 | SE_62828 | chr15:91350349-91418017 | Tonsil |
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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 |
GH15I090844 | chr15 | 91387875 | 91389289 |
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Enhancer Sequence | CTGTAACCTT GAACTTCTGG GCTCAAGCAA TTCTCCAGCC TCAGACTCCT GAGTAGCTGG 60 GACCACAGGC GCATACCACC ACGCCTGGCT AAAACTGGTT CCTTTTTTTT TTTTTTGAGA 120 CAGTGCCTTG TCCTGTCCCC CGGGCTGCAG TGCAATGGCA CAAACACTGC CCACTGCAGC 180 CTTGACCTCC TGGGCTCAAG CGATCTTCCC CTACAGCCTC CTGAGTAGCT GGCACCACAG 240 GCACGTGCCA CCATGCCTGG CCAAATTTTT TTTTTTTTTT TGTAGGGATG GAGTCTCACT 300 ATGTTGCCCA AGCTGGTCTC AATCTCCTGG GCTCAAGCCA TCCTCCTGCC TTGGCCTCCC 360 AAAGTGCTGG GATTAAAGGC ATGAGCCACC GTGCCCAGCC TAAAAATGGT CTTGATTCAA 420 TGAGTGAGTA AATGAAGCCT GTGCCCAGGG CCTGCCAGGC CCCCTGGGGC TGCCCACAGG 480 GTAAACACAG ACCCACACGG AGCCCCACTC CAGGCCTGGT CGAAAAAAAT GCTGCTCCAG 540 CTGAAGGCTT TCTCAGAGAA ATGACTCAGC CTGAGCACTC AGATGCAACT TCCACGTTTT 600 ATGGACTGAA GGTGCTTTCA TAACAGCTGG TGATGATGAG CCAGAGGCGG GCTATAAACA 660 GAGCGGTGAT CTGGTCCTGA ACACTCAGGT CTCAGCCCCC ACCCACAAGC AGGGCCTCTG 720 AGGCTGTGGC TTCTCCACAC TGGTGCTGCT TTGTGCTGGC AAATAGCACA GGCCCCCAAA 780 ATGACCTGGA GGCTCCTTAA CTGAGGAGGC AGATGAGTGA CAGGGCCAGA CCTGCAGCCT 840 CAAGGGCCTG GCTGTGCCCT CCCTAGCTCC CTTGGGCCTG GGAGCCTTCC ATGAACCTGT 900 GGCCTGGGAC CAAGAGCATG GGGGGCCTAG TGATGTGCCT GGTGGGGAGC GGGGAGTGCT 960 GCCAGCAATG ACAGTCCCGC TGGGGGGACG TGGTACAGAC TCACTGAGAC ACAGAACCCT 1020 GTGAGCAAGG GGGGTTCACT TAATCCTCCC TGAGGACTCA GACAGGTGGG CTGCAGGCAG 1080 TGGGGTAGCC TTGCCTCTCA CTCATGCCCA CCCACCCATT TGCTCATTCA TTCAGACAAG 1140 CGTGGATTGA GTATTTTCTT TTTTTTTCTT TTAAAGACAG GGTTTTGCTC TGTCGCTCAG 1200 GCTGAAGTGC AGTGGCATGA TCTCAGCTCA CTACAGCCTC ATCCTCCCAG 1250
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