Tag | Content |
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EnhancerAtlas ID | HS080-28477 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr5:72617510-72618550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr5:72617726-72617739 | GAACATTCCAGAA | - | 6.59 | RUNX1 | MA0002.2 | chr5:72618187-72618198 | GTCTGTGGTTT | + | 6.62 |
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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 |
GH05I073320 | chr5 | 72616822 | 72618700 |
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Enhancer Sequence | TTCACATTGG AGAGGTATTA CTTTTAAATC AGAAAATAAA ATGTTTAAAA ATTGCATAGA 60 TGTAGGCAGT ATAGCTTCTT AAAGTATCCA GTATTTGCCT TTGCCTTTTA TCCATGAACC 120 ACAATGTTTT GGGTGATTCA TGAATGATTC ACATCAAAAG CCCTGGCCTA TCTAAAATTT 180 CATATTTCTT CTTGCTCTTT CAGGTAGGAG ATTAATGAAC ATTCCAGAAT GAGACTATGG 240 CGTGGGAAGG AAGTGTGTAA TGAACCCAGG AGGATGCCTA GGAGATGTGT CCATTGTAGC 300 ATTCTAGGTG TGACCACAAA GTGCCCAGCA TGTGGCATTC TGAAGAAGGC CCTATGAGCT 360 CAGCATTCTA TTTCCTTTAC TCAGAATGGA AGCAGGAAGA TAGAATTCAA TTGCAAAATG 420 TTGGTCACTG ACTCTGAAAA GGATTCAAAT TACTGACAGC TTAAAGTAAT CAATGCTATG 480 AAAGCCATAA TTATCCCAAT ACTGCAAAGA TTTGGAGGTT TAACAACAAC AACAACAACA 540 AAAACCAGTT CTCCCAATCT GTGTCTTTCT GTCTGCATCT CTGTGGTTAC ATAACTAGAA 600 AAGGGCCGGT TCAGGAATGA ATCCCAGATG GCTCCGCTCA GTGTTTGCTT TGAAGTCGGT 660 TCAATTCGAT TTATCTGGTC TGTGGTTTGA GGATAGGGTG GAAGGATCCA ACTACACAAC 720 AGTGCCCAGA CCCCAGAGTA GGGACAGAAC ATCTGCTTCC TGGGCACAAG TGCATGAGGA 780 AAGGATTTAC CCTTCAAGGG TGTTGATTCT GATCCTGGCT ACATGGGGGA GAGGGGTGTG 840 GGGTGTTGCT TCCTGGCCTG CTCAGCCTGG GGTCTCGGGG GCTGCTTCTC ACCCTGCTGT 900 GTGAAAGCCA TGGCTGTAAG TCCCAGCCAA GCTTGGCCCC ACGGGTCTCC TACACCCAGG 960 AAGGTGTCAG ACCATCTCAG CTGGGTAAGG TCAAGTGGGG CCCCGGGGTT CCGCCCTTCA 1020 TTGTGGGTCT TGGTATTTAT 1040
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