Tag | Content |
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EnhancerAtlas ID | HS050-28776 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr17:41618080-41619010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6 | MA0463.2 | chr17:41618637-41618653 | CGTTCCTGGAGAGCAG | - | 6.04 | EWSR1-FLI1 | MA0149.1 | chr17:41618384-41618402 | CTTGCCTTTCTTCCTGCC | - | 6.17 | MNX1 | MA0707.1 | chr17:41618660-41618670 | TTTAATTACC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_69101 | chr17:41617858-41619537 | H9 |
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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 |
GH17I043538 | chr17 | 41616036 | 41619151 |
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Enhancer Sequence | CTGTCCACCT GCCCAGGGAT GCAAAGCCAG GCTCCCCACT GTGCCCTCTG GTCCATTCAG 60 AGGCAACATC CCCCAAGGTG GCAGGAAGCT GGGGTGATGG GAGCAGAGTG ACCAACATTT 120 CCCTCCCTCC TACTAGGCAA GAAGGGTCCC AAGGGAAAGG GTGGTGCAGA ACTCAGGGGT 180 GGCTGACGCA TTCCGGCCCC ACCCCTGGGG CCTCATTAAC TGCTACTTTC CATTGAGGTA 240 ATGGGCTGGG GGTATCTCTT GCTGGCGTCA CTGGTGCTGG AGAGCAGAGA ACCCTCAGCA 300 TCATCTTGCC TTTCTTCCTG CCTCGGGCCT GACAGTTTAA CCAGGGACCC CTCCAGGCCC 360 GGAATCCAGG AGGAGGCTTC CTCCAGCACA CAGACCACAC CCCAAAAGAG GTGGTGCCAT 420 CCTCTTCCCA GAGCCAGGAG AAATCTGTCC TAGCTCAGCC CCTCCCCCAA ACACTGGCCT 480 TCTCCCAAAG GGGTAGGCCA GGGCCCTCAG TCATCCAGAG ACTGTCAACA GGATAGAAAC 540 AGGAACACTG AGCCTCGCGT TCCTGGAGAG CAGGAGAATT TTTAATTACC ATGTTTCGTC 600 TTAAGTGTAC ACCACTCTCT TTATTTATTT GTTAACTTGG CTGAGTCTTG GCTGCCAAGC 660 CAGTGTGCCA GGGTCTGTCC CCAGCTCCAT CCCGGTACTA AGATGGAGTT TATCTGTCTG 720 GGGACGAGGC AGATGATTAA GGAGGGGGTG GGAAAAGTGC CAAGACAGCA TAATGCCCAG 780 AGAGAGAGAA AGAATTTTAG GGACTCTCCT TTCAAAAAGG GGGGTTAGTA AAAAAAGAGG 840 AGGGGCTTGG GGGGTCTCCC AAGCTGGATT CTGGAAGAAC TGAGAGGTTA AAACAGAGAT 900 ACACTGAAGC TCACCATAGG TTAGCCACCC 930
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